Medicare Program; FY 2024 Inpatient Psychiatric Facilities Prospective Payment System-Rate Update, 51054-51162 [2023-16083]
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Federal Register / Vol. 88, No. 147 / Wednesday, August 2, 2023 / Rules and Regulations
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 412
[CMS–1783–F]
RIN 0938–AV06
Medicare Program; FY 2024 Inpatient
Psychiatric Facilities Prospective
Payment System—Rate Update
Centers for Medicare &
Medicaid Services (CMS), Department
of Health and Human Services (HHS).
ACTION: Final rule.
AGENCY:
This final rule updates the
prospective payment rates, the outlier
threshold, and the wage index for
Medicare inpatient hospital services
provided by Inpatient Psychiatric
Facilities (IPF), which include
psychiatric hospitals and excluded
psychiatric units of an acute care
hospital or critical access hospital.
Additionally, this final rule rebases and
revises the IPF market basket to reflect
a 2021 base year. These changes will be
effective for IPF discharges occurring
during the Fiscal Year (FY) beginning
October 1, 2023 through September 30,
2024 (FY 2024). In addition, this final
rule discusses quality measures and
reporting requirements under the
Inpatient Psychiatric Facilities Quality
Reporting (IPFQR) Program with
changes beginning with the FY 2025
payment determination through changes
beginning with the FY 2028 payment
determination.
DATES: These regulations are effective
on October 1, 2023.
FOR FURTHER INFORMATION CONTACT:
Mollie Knight (410) 786–7948 or Bridget
Dickensheets (410) 786–8670, for
information regarding the market basket
update or the labor-related share.
Nick Brock (410) 786–5148 or Theresa
Bean (410) 786–2287, for information
regarding the regulatory impact
analysis.
Lauren Lowenstein-Turner, (410)
786–4507, for information regarding the
inpatient psychiatric facilities quality
reporting program.
SUPPLEMENTARY INFORMATION:
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SUMMARY:
Availability of Certain Tables
Exclusively Through the Internet on the
CMS Website
Addendum A to this final rule
summarizes the fiscal year (FY) 2024
IPF PPS payment rates, outlier
threshold, cost of living adjustment
factors (COLA) for Alaska and Hawaii,
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national and upper limit cost-to-charge
ratios, and adjustment factors. In
addition, Addenda B to this final rule
show the complete listing of ICD–10
Clinical Modification (CM) and
Procedure Coding System (PCS) codes,
the FY 2024 IPF PPS comorbidity
adjustment, and electroconvulsive
therapy (ECT) procedure codes.
Addenda A and B to this final rule are
available online at: https://
www.cms.gov/Medicare/Medicare-Feefor-Service-Payment/
InpatientPsychFacilPPS/tools.html.
Tables setting forth the FY 2024 Wage
Index for Urban Areas Based on Core
Based Statistical Area (CBSA) Labor
Market Areas and the FY 2024 Wage
Index Based on CBSA Labor Market
Areas for Rural Areas are available
exclusively through the internet, on the
CMS website at https://www.cms.gov/
Medicare/Medicare-Fee-for-ServicePayment/IPFPPS/WageIndex.html.
I. Executive Summary
A. Purpose
This final rule rebases and revises the
market basket for the Inpatient
Psychiatric Facility Prospective
Payment System (IPF PPS) to reflect a
2021 base year, revises the labor-related
share, and updates the prospective
payment rates, the outlier threshold,
and the wage index for Medicare
inpatient hospital services provided by
Inpatient Psychiatric Facilities (IPFs) for
discharges occurring during FY 2024,
(beginning October 1, 2023 through
September 30, 2024). This rule also
modifies our regulations to make it
easier for hospitals to open new
excluded psychiatric units paid under
the IPF PPS. In addition, this final rule
includes a summary of the public
comments received to inform revisions
to IPF PPS payments for FY 2025, as
required by the Consolidated
Appropriations Act, 2023 (hereafter
referred to as CAA, 2023) (Pub. L. 117328). Lastly, this final rule discusses
quality measures and reporting
requirements under the Inpatient
Psychiatric Facilities Quality Reporting
(IPFQR) Program.
B. Summary of the Major Provisions
1. Inpatient Psychiatric Facilities
Prospective Payment System (IPF PPS)
For the IPF PPS, we are finalizing our
proposal to—
• Modify the regulations to allow the
status of a hospital psychiatric unit to be
changed from not excluded to excluded,
and therefore paid under the IPF PPS,
at any time during a cost reporting
period if certain requirements are met.
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• Rebase and revise the IPF market
basket to reflect a 2021 base year.
• Adjust the 2021-based IPF market
basket update (3.5 percent) for
economy-wide productivity (0.2
percentage point) as required by section
1886(s)(2)(A)(i) of the Social Security
Act (the Act), resulting in a final IPF
payment rate update of 3.3 percent for
FY 2024.
• Make technical rate setting updates:
The IPF PPS payment rates will be
adjusted annually for inflation, as well
as statutory and other policy factors.
This rule updates:
++ The IPF PPS Federal per diem base
rate from $865.63 to $895.63.
++ The IPF PPS Federal per diem base
rate for providers who failed to report
quality data to $878.29.
++ The electroconvulsive therapy
(ECT) payment per treatment from
$372.67 to $385.58 .
++ The ECT payment per treatment
for providers who failed to report
quality data to $378.12.
++ The labor-related share from 77.4
percent to 78.7 percent.
++ The wage index budget-neutrality
factor to 1.0016.
++ The fixed dollar loss threshold
amount from $24,630 to $33,470 to
maintain estimated outlier payments at
2 percent of total estimated aggregate
IPF PPS payments.
2. Inpatient Psychiatric Facilities
Quality Reporting (IPFQR) Program
For the IPFQR Program, we are
finalizing our proposals to—
• Adopt the Facility Commitment to
Health Equity measure beginning with
the FY 2026 payment determination;
• Adopt the Screening for Social
Drivers of Health measure beginning
with voluntary reporting of calendar
year (CY) 2024 data followed by
mandatory reporting of CY 2025 data for
the FY 2027 payment determination;
• Adopt the Screen Positive Rate for
Social Drivers of Health measure
beginning with voluntary reporting of
CY 2024 data followed by mandatory
reporting of CY 2025 data for the FY
2027 payment determination;
• Adopt the Psychiatric Inpatient
Experience (PIX) survey to measure
patient experience of care in the IPF
setting beginning with voluntary
reporting of CY 2025 data followed by
mandatory reporting of CY 2026 data for
the FY 2028 payment determination;
• Modify the Coronavirus disease
2019 (COVID–19) Vaccination Coverage
Among Health Care Personnel (HCP)
measure to align the measure with
updated measure specifications
developed by the Centers for Disease
Control and Prevention (CDC), which
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II. Background
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A. Overview of the Legislative
Requirements of the IPF PPS
Section 124 of the Medicare,
Medicaid, and State Children’s Health
Insurance Program Balanced Budget
Refinement Act of 1999 (BBRA) (Pub. L.
106–113) required the establishment
and implementation of an IPF PPS.
Specifically, section 124 of the BBRA
mandated that the Secretary of the
Department of Health and Human
Services (the Secretary) develop a per
diem payment perspective system (PPS)
for inpatient hospital services furnished
in psychiatric hospitals and excluded
psychiatric units including an adequate
patient classification system that reflects
the differences in patient resource use
and costs among psychiatric hospitals
and excluded psychiatric units.
‘‘Excluded psychiatric unit’’ means a
psychiatric unit of an acute care
hospital or of a Critical Access Hospital
(CAH), which is excluded from payment
under the Inpatient Prospective
Payment System (IPPS) or CAH
payment system, respectively. These
excluded psychiatric units will be paid
under the IPF PPS.
Section 405(g)(2) of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) (Pub.
L. 108–173) extended the IPF PPS to
psychiatric distinct part units of CAHs.
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• Remove the following two measures
beginning with the FY 2025 payment
determination and subsequent years:
++ Patients Discharged on Multiple
Antipsychotic Medications with
Appropriate Justification (HBIPS–5);
and
++ Tobacco Use Brief Intervention
Provided or Offered and Tobacco Use
Brief Intervention Provided (TOB–2/2a)
measure;
• Adopt a data validation pilot
program starting with data submitted in
CY 2025 and continuing until a full data
validation program is proposed and
adopted in future rulemaking; and
• Codify the IPFQR Program’s
procedural requirements related to
statutory authority, participation and
withdrawal, data submission, quality
measure retention and removal,
extraordinary circumstances exceptions,
and public reporting at 42 CFR 412.433
Procedural requirements under the
IPFQR Program.
Sections 3401(f) and 10322 of the
Patient Protection and Affordable Care
Act (Pub. L. 111–148) as amended by
section 10319(e) of that Act and by
section 1105(d) of the Health Care and
Education Reconciliation Act of 2010
(Pub. L. 111–152) (hereafter referred to
jointly as ‘‘the Affordable Care Act’’)
added subsection (s) to section 1886 of
the Social Security Act (the Act).
Section 1886(s)(1) of the Act titled,
‘‘Reference to Establishment and
Implementation of System,’’ refers to
section 124 of the BBRA, which relates
to the establishment of the IPF PPS.
Section 1886(s)(2)(A)(i) of the Act
requires the application of the
productivity adjustment described in
section 1886(b)(3)(B)(xi)(II) of the Act to
the IPF PPS for the rate year (RY)
beginning in 2012 (that is, a RY that
coincides with a FY) and each
subsequent RY.
Section 1886(s)(2)(A)(ii) of the Act
required the application of an ‘‘other
adjustment’’ that reduced any update to
an IPF PPS base rate by a percentage
point amount specified in section
1886(s)(3) of the Act for the RY
beginning in 2010 through the RY
beginning in 2019. As noted in the FY
2020 IPF PPS final rule, for the RY
beginning in 2019, section 1886(s)(3)(E)
of the Act required that the other
adjustment reduction be equal to 0.75
percentage point; that was the final year
the statute required the application of
this adjustment. Because FY 2021 was a
RY beginning in 2020, FY 2021 was the
first-year section 1886(s)(2)(A)(ii) of the
Act did not apply since its enactment.
Sections 1886(s)(4)(A) through (D) of
the Act require that for RY 2014 and
each subsequent RY, IPFs that fail to
report required quality data with respect
to such a RY will have their annual
update to a standard Federal rate for
discharges reduced by 2.0 percentage
points. This may result in an annual
update being less than 0.0 for a RY, and
may result in payment rates for the
upcoming RY being less than such
payment rates for the preceding RY.
Any reduction for failure to report
required quality data will apply only to
the RY involved, and the Secretary will
not consider such reduction in
computing the payment amount for a
subsequent RY. Section 4125 of division
FF, title IV, subtitle C, the CAA, 2023
requires that not later than FY 2028
each IPF will submit data through the
use of a standardized assessment
instrument which includes data on
functional status; cognitive function;
special services treatments, and
interventions for psychiatric conditions;
impairments; and other categories
deemed appropriate. In addition,
section 4125 of the CAA, 2023 requires
that a patients’ perspective of care
quality measure be added to the IPFQR
Program not later than for FY 2031.
Information regarding the newly
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C. Summary of Impacts
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ER02AU23.000
address refinements reflecting the
availability, and FDA authorization, of
Moderna and Pfizer-BioNTech COVID–
19 vaccines for use as booster doses,
beginning with fourth quarter CY 2023
data for the FY 2025 payment
determination and, following this first
single-quarter reporting period,
reporting for the full calendar year
beginning with CY 2024 data for the FY
2026 payment determination;
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adopted Psychiatric Inpatient
Experience (PIX) survey measure is
provided in section VI.D.5 of this final
rule.
Section 4125 of the CAA, 2023 also
requires revisions to the Medicare
prospective payment system (PPS) for
psychiatric hospitals and psychiatric
units. Specifically, section 4125(a) of
the CAA, 2023 amends section 1886(s)
of the Act by adding a new paragraph
(5) that requires the Secretary to collect
data and information beginning no later
than October 1, 2023, as the Secretary
determines appropriate, to inform
revisions to IPF PPS payments. In
addition, the Secretary is required to
implement revisions to the methodology
for determining the payment rates under
the IPF PPS for FY 2025 as the Secretary
determines appropriate.
To implement and periodically
update the IPF PPS, we have published
various proposed and final rules and
notices in the Federal Register. For
more information regarding these
documents, see the CMS website at
https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
InpatientPsychFacilPPS/
index.html?redirect=/
InpatientPsychFacilPPS/.
B. Overview of the IPF PPS
On November 15, 2004, we published
the IPF PPS final rule in the Federal
Register (69 FR 66922). The November
2004 IPF PPS final rule established the
IPF PPS, as required by section 124 of
the BBRA and codified at 42 CFR part
412, subpart N. The November 2004 IPF
PPS final rule set forth the Federal per
diem base rate for the implementation
year (the 18-month period from January
1, 2005 through June 30, 2006), and
provided payment for the inpatient
operating and capital costs to IPFs for
covered psychiatric services they
furnish (that is, routine, ancillary, and
capital costs, but not costs of approved
educational activities, bad debts, and
other services or items that are outside
the scope of the IPF PPS). Covered
psychiatric services include services for
which benefits are provided under the
fee-for-service Part A (Hospital
Insurance Program) of the Medicare
program.
The IPF PPS established the Federal
per diem base rate for each patient day
in an IPF derived from the national
average daily routine operating,
ancillary, and capital costs in IPFs in FY
2002. The average per diem cost was
updated to the midpoint of the first year
under the IPF PPS, standardized to
account for the overall positive effects of
the IPF PPS payment adjustments, and
adjusted for budget-neutrality.
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The Federal per diem payment under
the IPF PPS is comprised of the Federal
per diem base rate described previously
and certain patient- and facility-level
payment adjustments for characteristics
that were found in the regression
analysis to be associated with
statistically significant per diem cost
differences; with statistical significance
defined as p less than 0.05. A complete
discussion of the regression analysis
that established the IPF PPS adjustment
factors can be found in the November
2004 IPF PPS final rule (69 FR 66933
through 66936).
The patient-level adjustments include
age, Diagnosis-Related Group (DRG)
assignment, and comorbidities, as well
as adjustments to reflect higher per
diem costs at the beginning of a
patient’s IPF stay and lower costs for
later days of the stay. Facility-level
adjustments include adjustments for the
IPF’s wage index, rural location,
teaching status, a cost-of-living
adjustment for IPFs located in Alaska
and Hawaii, and an adjustment for the
presence of a qualifying emergency
department (ED).
The IPF PPS has additional payment
policies for outlier cases, interrupted
stays, and a per treatment payment for
patients who undergo ECT. During the
IPF PPS mandatory 3-year transition
period, stop-loss payments were also
provided; however, since the transition
ended as of January 1, 2008, these
payments are no longer available.
C. Annual Requirements for Updating
the IPF PPS
Section 124 of the BBRA did not
specify an annual rate update strategy
for the IPF PPS and was broadly written
to give the Secretary discretion in
establishing an update methodology. In
the November 2004 IPF PPS final rule
(69 FR 66922), we implemented the IPF
PPS using the following update strategy:
• Calculate the final Federal per diem
base rate to be budget-neutral for the 18month period of January 1, 2005
through June 30, 2006.
• Use a July 1 through June 30 annual
update cycle.
• Allow the IPF PPS first update to be
effective for discharges on or after July
1, 2006 through June 30, 2007.
In developing the IPF PPS, and to
ensure that the IPF PPS can account
adequately for each IPF’s case-mix, we
performed an extensive regression
analysis of the relationship between the
per diem costs and certain patient and
facility characteristics to determine
those characteristics associated with
statistically significant cost differences
on a per diem basis. That regression
analysis is described in detail in our
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November 28, 2003 IPF PPS proposed
rule (68 FR 66923; 66928 through
66933) and our November 15, 2004 IPF
PPS final rule (69 FR 66933 through
66960). For characteristics with
statistically significant cost differences,
we used the regression coefficients of
those variables to determine the size of
the corresponding payment
adjustments.
In the November 2004 IPF PPS final
rule, we explained the reasons for
delaying an update to the adjustment
factors, derived from the regression
analysis, including waiting until we
have IPF PPS data that yields as much
information as possible regarding the
patient-level characteristics of the
population that each IPF serves. We
indicated that we did not intend to
update the regression analysis and the
patient-level and facility-level
adjustments until we complete that
analysis. Until that analysis is complete,
we stated our intention to publish a
notice in the Federal Register each
spring to update the IPF PPS (69 FR
66966).
On May 6, 2011, we published a final
rule in the Federal Register titled,
‘‘Inpatient Psychiatric Facilities
Prospective Payment System—Update
for Rate Year Beginning July 1, 2011 (RY
2012)’’ (76 FR 26432), which changed
the payment rate update period to a RY
that coincides with a FY update.
Therefore, final rules are now published
in the Federal Register in the summer
to be effective on October 1st. When
proposing changes in IPF payment
policy, a proposed rule would be issued
in the spring and the final rule in the
summer to be effective on October 1st.
For a detailed list of updates to the IPF
PPS, we refer readers to our regulations
at 42 CFR 412.428.
The most recent IPF PPS annual
update was published in a final rule on
July 29, 2022 in the Federal Register
titled, ‘‘Medicare Program; FY 2023
Inpatient Psychiatric Facilities
Prospective Payment System—Rate
Update and Quality Reporting—Request
for Information’’ (87 FR 46846), which
updated the IPF PPS payment rates for
FY 2023. That final rule updated the IPF
PPS Federal per diem base rates that
were published in the FY 2022 IPF PPS
Rate Update final rule (86 FR 42608) in
accordance with our established
policies.
III. Analysis of and Responses to Public
Comments
We received 2,506 public comments
that pertain to proposed IPF PPS
payment policies, requests for
information, and the proposed updates
to the IPFQR Program. Comments were
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from Inpatient Psychiatric Facilities,
health systems, national and state level
provider and patient advocacy
organizations, the Medicare Payment
Advisory Commission (MedPAC), and
individuals. We reviewed each
comment and grouped related
comments, after which we placed them
in categories based on subject matter or
section(s) of the regulation affected.
Summaries of the public comments
received and our responses to those
comments are provided in the
appropriate sections in the preamble of
this final rule.
IV. Provisions of the FY 2024 IPF PPS
Final Rule and Responses to Comments
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A. Rebasing and Revising of the Market
Basket for the IPF PPS
1. Background
Originally, the input price index used
to develop the IPF PPS was the
Excluded Hospital with Capital market
basket. This market basket was based on
1997 Medicare cost reports for
Medicare-participating inpatient
rehabilitation facilities (IRFs), IPFs,
long-term care hospitals (LTCHs),
cancer hospitals, and children’s
hospitals. Although ‘‘market basket’’
technically describes the mix of goods
and services used in providing health
care at a given point in time, this term
is also commonly used to denote the
input price index (that is, cost category
weights and price proxies) derived from
that market basket. Accordingly, the
term ‘‘market basket,’’ as used in this
document, refers to an input price
index.
Since the IPF PPS inception, the
market basket used to update IPF PPS
payments has been rebased and revised
to reflect more recent data on IPF cost
structures. We last rebased and revised
the market basket applicable to the IPF
PPS in the FY 2020 IPF PPS final rule
(84 FR 38426 through 38447), where we
adopted a 2016-based IPF market basket.
The 2016-based IPF market basket used
Medicare cost report data for both
Medicare-participating freestanding
psychiatric hospitals and hospital-based
psychiatric units. References to the
historical market baskets used to update
IPF PPS payments are listed in the FY
2016 IPF PPS final rule (80 FR 46656).
For the FY 2024 IPF PPS proposed rule,
we proposed to rebase and revise the
IPF market basket to reflect a 2021 base
year.
2. Overview of the 2021-Based IPF
Market Basket
The 2021-based IPF market basket is
a fixed-weight, Laspeyres-type price
index. A Laspeyres price index
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measures the change in price, over time,
of the same mix of goods and services
purchased in the base period. Any
changes in the quantity or mix of goods
and services (that is, intensity)
purchased over time relative to a base
period are not measured.
The index itself is constructed in
three steps. First, a base period is
selected (in the proposed rule, we
proposed to use 2021 as the base period)
and total base period costs are estimated
for a set of mutually exclusive and
exhaustive cost categories. Each
category is calculated as a proportion of
total costs. These proportions are called
cost weights. Second, each cost category
is matched to an appropriate price or
wage variable, referred to as a price
proxy. In nearly every instance, these
price proxies are derived from publicly
available statistical series that are
published on a consistent schedule
(preferably at least on a quarterly basis).
Finally, the cost weight for each cost
category is multiplied by the level of its
respective price proxy. The sum of these
products (that is, the cost weights
multiplied by their price index levels)
for all cost categories yields the
composite index level of the market
basket in a given period. Repeating this
step for other periods produces a series
of market basket levels over time.
Dividing an index level for a given
period by an index level for an earlier
period produces a rate of growth in the
input price index over that timeframe.
As noted, the market basket is
described as a fixed-weight index
because it represents the change in price
over time of a constant mix (quantity
and intensity) of goods and services
needed to provide IPF services. The
effects on total costs resulting from
changes in the mix of goods and
services purchased subsequent to the
base period are not measured. For
example, an IPF hiring more nurses after
the base period to accommodate the
needs of patients will increase the
volume of goods and services purchased
by the IPF but will not be factored into
the price change measured by a fixedweight IPF market basket. Only when
the index is rebased will changes in the
quantity and intensity be captured, with
those changes being reflected in the cost
weights. Therefore, we rebase the
market basket periodically so that the
cost weights reflect recent changes in
the mix of goods and services that IPFs
purchase to furnish inpatient care
between base periods.
3. Rebasing and Revising of the IPF
Market Basket
As discussed in the FY 2020 IPF PPS
final rule (84 FR 38426 through 38447),
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the 2016-based IPF market basket
reflects the Medicare cost reports for
both freestanding and hospital-based
IPFs. Beginning with FY 2024, we
proposed to rebase and revise the IPF
market basket to a 2021 base year
reflecting the 2021 Medicare cost report
data submitted by both freestanding and
hospital-based IPFs. We provide a
detailed description of our proposed
methodology used to develop the 2021based IPF market basket below. This
proposed methodology is generally
similar to the methodology used to
develop the 2016-based IPF market
basket. We solicited public comment on
our proposed methodology for
developing the 2021-based IPF market
basket.
Comment: Several commenters
supported CMS’s proposal to rebase and
revise the market basket to reflect more
recent data, noting that the changes in
the cost weights were consistent with
their expectations or experience. One
commenter, however, proposed that
CMS wait to rebase the IPF market
basket until FY 2022 data is available.
The commenter stated that, due to the
increased demand for hospital care
during the initial year following the
outbreak of COVID–19 in the United
States, they assume that a base year of
FY 2021 would not necessarily reflect
costs in FY 2024. Though inflation was
particularly high during FY 2021, the
commenter noted that FY 2022 would
be further removed from the initial
outbreak of COVID–19 in the United
States and the massive changes in
healthcare that occurred during that
time. Similarly, one commenter
supported the proposal to rebase but
recommended CMS plan to rebase and
revise the market basket and laborrelated share to reflect a 2023 base year
to fully incorporate the cost structures
from the Public Health Emergency
(PHE) as well as the evolving hospital
workforce shortage.
Response: We appreciate the
commenters’ support regarding the
proposed IPF market basket. For the
proposed rebasing and revising, we used
the most current and complete set of
Medicare cost report data (2021) at the
time of rulemaking to determine the
major base year cost weights (Wages and
Salaries, Employee Benefits, Contract
Labor, Professional Liability Insurance,
Pharmaceuticals, Home Office/Related
Organization Contract Labor, and
Capital).
As stated in the FY 2024 IPF PPS
proposed rule (88 FR 21241), many
commenters expressed concern in
response to the FY 2023 IPF PPS
proposed rule, in which we did not
propose to rebase the IPF market basket.
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The commenters stated at that time that
the 2016-based IPF market basket did
not reflect the current costs of IPFs,
particularly the use of contract labor.
Therefore, based on the typical
timeframe for rebasing the market
baskets and in response to commenters’
concerns expressed in FY 2023 IPF
rulemaking, we proposed to rebase and
revise the IPF market basket for FY
2024. We understand the commenters’
concerns that the impact of the PHE
may have resulted in increased costs
compared to 2016. However, we believe
it is appropriate to rebase the market
basket regularly and to reflect more
recent IPF cost structures. It has been
our longstanding practice to rebase the
IPF market basket (as well as other CMS
market baskets) on a regular basis to
ensure it reflects a more up-to-date
input cost structure of IPFs so that the
price change in the market basket best
reflects input prices faced by IPFs.
Because complete 2022 IPF Medicare
cost report data is currently unavailable,
we believe it is more appropriate to
update the base year cost weights to
2021 to reflect changes over this period
rather than to delay the rebasing for
another year or two in order to use 2022
or 2023 Medicare cost report data as
suggested by the commenter. We
regularly rebase every 4 to 5 years
because more recent data is typically
more reflective of IPF cost structures.
Therefore, we are using the most recent
cost report data we have, which is 2021
cost report data, as it is more reflective
of IPF cost structures than 2016 data.
For example, the 2021-based IPF market
basket reflects the higher compensation
cost weight (as compared to the 2016based IPF market basket) as a result of
an increase in the contract labor cost
weight (calculated using the 2021
Medicare cost report data) as noted by
the commenters in response to the FY
2023 IPF proposed rule (87 FR 46849).
Additionally, we will continue to
monitor the Medicare cost report data to
assess whether a more frequent rebasing
of the IPF market basket is appropriate
through future notice and comment
rulemaking.
Final Decision: We are finalizing our
proposal to rebase the IPF market basket
to reflect a 2021 base year for FY 2024.
We provide a summary of the more
detailed public comments received on
our proposed methodology for
developing the 2021-based IPF market
basket and our responses in the
following sections.
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a. Development of Cost Categories and
Weights for the 2021-Based IPF Market
Basket
(1) Use of Medicare Cost Report Data
We proposed a 2021-based IPF market
basket that consists of seven major cost
categories and a residual derived from
the 2021 Medicare cost reports (CMS
Form 2552–10, OMB No. 0938–0050) for
freestanding and hospital-based IPFs.
The seven major cost categories are
Wages and Salaries, Employee Benefits,
Contract Labor, Pharmaceuticals,
Professional Liability Insurance (PLI),
Home Office/Related Organization
Contract Labor, and Capital. The cost
reports include providers whose cost
reporting period began on or after
October 1, 2020 and before October 1,
2021. As noted previously, the current
IPF market basket is based on 2016
Medicare cost reports and therefore,
reflects the 2016 cost structure for IPFs.
As described in the FY 2023 IPF PPS
final rule (87 FR 46849), we received
comments on the FY 2023 IPF PPS
proposed rule (87 FR 19418 through
19419) where stakeholders expressed
concern that the proposed market basket
update inadequately reflected the input
price inflation experienced by IPFs,
particularly as a result of the COVID–19
PHE. These commenters stated that the
PHE, along with inflation, has
significantly driven up operating costs.
Specifically, some commenters noted
changes to labor markets that led to the
use of more contract labor, a trend that
we verified in analyzing the Medicare
cost report data through 2021.
Therefore, we believe it is appropriate to
incorporate more recent data to reflect
updated cost structures for IPFs, and so
we proposed to use 2021 as the base
year, because we believe that the
Medicare cost reports for this year
represent the most recent complete set
of Medicare cost report data available
for developing the proposed IPF market
basket at the time of this rulemaking.
Given the potential impact of the PHE
on the Medicare cost report data, we
will continue to monitor these data
going forward, and any changes to the
IPF market basket will be proposed in
future rulemaking.
Similar to the Medicare cost report
data used to develop the 2016-based IPF
market basket, the Medicare cost report
data for 2021 show large differences
between some providers’ Medicare
length of stay (LOS) and total facility
LOS. Our goal has always been to
measure cost weights that are reflective
of case mix and practice patterns
associated with providing services to
Medicare beneficiaries. Therefore, we
proposed to limit our selection of
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Medicare cost reports used in the 2021based IPF market basket to those
facilities that had a Medicare LOS
within a comparable range of their total
facility average LOS. The Medicare
average LOS for freestanding IPFs is
calculated from data reported on line 14
of Worksheet S–3, part I. The Medicare
average LOS for hospital-based IPFs is
calculated from data reported on line 16
of Worksheet S–3, part I. To derive the
2021-based IPF market basket, for those
IPFs with an average facility LOS of
greater than or equal to 15 days, we
proposed to include IPFs where the
Medicare LOS is within 50 percent
(higher or lower) of the average facility
LOS. For those IPFs whose average
facility LOS is less than 15 days, we
proposed to include IPFs where the
Medicare LOS is within 95 percent
(higher or lower) of the facility LOS. We
proposed to apply this LOS edit to the
data for IPFs to exclude providers that
serve a population whose LOS will
indicate that the patients served are not
consistent with a LOS of a typical
Medicare patient. This is the same LOS
edit applied to the 2016-based IPF
market basket.
Applying these trims to the
approximate 1,370 total cost reports
(freestanding and hospital-based)
resulted in roughly 1,250 IPF Medicare
cost reports with an average Medicare
LOS of 13 days, average facility LOS of
10 days, and Medicare utilization (as
measured by Medicare inpatient IPF
days as a percentage of total facility
days) of 16 percent. Providers excluded
from the 2021-based IPF market basket
(about 120 Medicare cost reports) had
an average Medicare LOS of 21 days,
average facility LOS of 41 days, and a
Medicare utilization of 3 percent. Of
those excluded, about 62 percent of
these were freestanding providers; on
the other hand, freestanding providers
represent about 38 percent of all IPFs.
We note that 70 percent of those
excluded from the 2016-based IPF
market basket using this LOS edit were
freestanding providers.
We then proposed to use the cost
reports for IPFs that met this
requirement to calculate the costs for
the seven major cost categories (Wages
and Salaries, Employee Benefits,
Contract Labor, Professional Liability
Insurance, Pharmaceuticals, Home
Office/Related Organization Contract
Labor, and Capital) for the market
basket. These are the same categories
used for the 2016-based IPF market
basket. Also, as described in section
IV.A.3.a.(4) of this final rule, and as
done for the 2016-based IPF market
basket, we proposed to use the Medicare
cost report data to calculate the detailed
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capital cost weights for the
Depreciation, Interest, Lease, and Other
Capital-related cost categories. We also
proposed to rename the Home Office
Contract Labor cost category to the
Home Office/Related Organization
Contract Labor cost category to be more
consistent with the Medicare cost report
instructions.
Similar to the 2016-based IPF market
basket major cost weights, for the
majority of the 2021-based IPF market
basket cost weights, we proposed to
divide the costs for each cost category
by total Medicare allowable costs
(routine, ancillary and capital)—costs
that are eligible for payment through the
IPF PPS (we noted that we use total
facility medical care costs as the
denominator to derive both the PLI and
Home Office/Related Organization
Contract Labor cost weights). We next
describe our proposed methodology for
deriving the cost levels used to derive
the 2021-based IPF market basket.
(a) Total Medicare Allowable Costs
For freestanding IPFs, we proposed
that total Medicare allowable costs
would be equal to the sum of total costs
for the Medicare allowable cost centers
as reported on Worksheet B, part I,
column 26, lines 30 through 35, 50
through 76 (excluding 52 and 75), 90
through 91, and 93.
For hospital-based IPFs, we proposed
that total Medicare allowable costs
would be equal to the total costs for the
IPF inpatient unit after the allocation of
overhead costs (Worksheet B, part I,
column 26, line 40) and a proportion of
total ancillary costs reported on
Worksheet B, part I, column 26, lines 50
through 76 (excluding 52 and 75), 90
through 91, and 93.
We proposed to calculate total
ancillary costs attributable to the
hospital-based IPF by first deriving an
‘‘IPF ancillary ratio’’ for each ancillary
cost center. The IPF ancillary ratio is
defined as the ratio of IPF Medicare
ancillary costs for the cost center (as
reported on Worksheet D–3, column 3
for hospital-based IPFs) to total
Medicare ancillary costs for the cost
center (equal to the sum of Worksheet
D–3, column 3 for all relevant PPSs [that
is, IPPS, IRF, IPF and skilled nursing
facility (SNF)]). For example, if hospitalbased IPF Medicare laboratory costs
represent about 2 percent of the total
Medicare laboratory costs for the entire
facility, then the IPF ancillary ratio for
laboratory costs would be 2 percent. We
believe it is appropriate to use only a
portion of the ancillary costs in the
market basket cost weight calculations
since the hospital-based IPF only
utilizes a portion of the facility’s
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ancillary services. We believe the ratio
of reported IPF Medicare costs to
reported total Medicare costs provides a
reasonable estimate of the ancillary
services utilized, and costs incurred, by
the hospital-based IPF. We proposed
that this IPF ancillary ratio for each cost
center is also used to calculate Wages
and Salaries and Capital costs as
described below.
Then, for each ancillary cost center,
we proposed to multiply the IPF
ancillary ratio for the given cost center
by the total facility ancillary costs for
that specific cost center (as reported on
Worksheet B, part I, column 26) to
derive IPF ancillary costs. For example,
the 2 percent IPF ancillary ratio for
laboratory cost center would be
multiplied by the total ancillary costs
for laboratory (Worksheet B, part I,
column 26, line 60). The IPF ancillary
costs for each cost center are then added
to total costs for the IPF inpatient unit
after the allocation of overhead costs
(Worksheet B, part I, column 26, line 40)
to derive total Medicare allowable costs.
We proposed to use these methods to
derive levels of total Medicare allowable
costs for IPF providers. This is the same
methodology used for the 2016-based
IPF market basket. We proposed that
these total Medicare allowable costs for
the IPF will be the denominator for the
cost weight calculations for the Wages
and Salaries, Employee Benefits,
Contract Labor, Pharmaceuticals, and
Capital cost weights. With this work
complete, we then set about deriving
cost levels for the seven major cost
categories and then derive a residual
cost weight reflecting all other costs not
classified.
(b) Wages and Salaries Costs
For freestanding IPFs, we proposed to
derive Wages and Salaries costs as the
sum of routine inpatient salaries
(Worksheet A, column 1, lines 30
through 35), ancillary salaries
(Worksheet A, column 1, lines 50
through 76 (excluding 52 and 75), 90
through 91, and 93), and a proportion of
overhead (or general service cost centers
in the Medicare cost reports) salaries.
Since overhead salary costs are
attributable to the entire IPF, we only
include the proportion attributable to
the Medicare allowable cost centers. We
proposed to estimate the proportion of
overhead salaries that are attributed to
Medicare allowable costs centers by
multiplying the ratio of Medicare
allowable area salaries (Worksheet A,
column 1, lines 30 through 35, 50
through 76 (excluding 52 and 75), 90
through 91, and 93) to total nonoverhead salaries (Worksheet A, column
1, line 200 less Worksheet A, column 1,
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51059
lines 4 through 18) times total overhead
salaries (Worksheet A, column 1, lines
4 through 18). This is a similar
methodology as used in the 2016-based
IPF market basket.
For hospital-based IPFs, we proposed
to derive Wages and Salaries costs as the
sum of the following salaries
attributable to the hospital-based IPF:
Inpatient routine salary costs
(Worksheet A, column 1, line 40);
overhead salary costs; ancillary salary
costs; and a portion of overhead salary
costs attributable to the ancillary
departments.
(i) Overhead Salary Costs
We proposed to calculate the portion
of overhead salary cost attributable to
hospital-based IPFs by first calculating
an IPF overhead salary ratio, which is
equal to the ratio of total facility
overhead salaries (as reported on
Worksheet A, column 1, lines 4–18) to
total facility noncapital overhead costs
(as reported on Worksheet A, column 1
and 2, lines 4–18). We then proposed to
multiply this IPF overhead salary ratio
by total noncapital overhead costs (sum
of Worksheet B, part I, columns 4
through 18, line 40, less Worksheet B,
part II, columns 4 through 18, line 40).
This methodology assumes the
proportion of total costs related to
salaries for the overhead cost center is
similar for all inpatient units (that is,
acute inpatient or inpatient psychiatric).
(ii) Ancillary Salary Costs
We proposed to calculate hospitalbased IPF ancillary salary costs for a
specific cost center (Worksheet A,
column 1, lines 50 through 76
(excluding 52 and 75), 90 through 91,
and 93) as salary costs from Worksheet
A, column 1, multiplied by the IPF
ancillary ratio for each cost center as
described in section IV.A.3.a.(1)(a) of
this final rule. The sum of these costs
represents hospital-based IPF ancillary
salary costs.
(iii) Overhead Salary Costs for Ancillary
Cost Centers
We proposed to calculate the portion
of overhead salaries attributable to each
ancillary department (lines 50 through
76 (excluding 52 and 75), 90 through 91,
and 93) by first calculating total
noncapital overhead cost attributable to
each specific ancillary department (sum
of Worksheet B, part I, columns 4–18,
less Worksheet B, part II, column 26).
We then identify the portion of these
total noncapital overhead cost for each
ancillary department that is attributable
to the hospital-based IPF by multiplying
these costs by the IPF ancillary ratio as
described in section IV.A.3.a.(1)(a) of
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this final rule. We then sum these
estimated IPF Medicare allowable
noncapital overhead costs for all
ancillary departments (cost centers 50
through 76, 90 through 91, and 93).
Finally, we then identify the portion of
these IPF Medicare allowable noncapital
overhead cost that are attributable to
Wages and Salaries by multiplying these
costs by the IPF overhead salary ratio as
described in section IV.A.3.a.(1)(b)(i) of
this final rule. This is the same
methodology used to derive the 2016based IPF market basket.
(c) Employee Benefits Costs
Effective with the implementation of
CMS Form 2552–10, we began
collecting Employee Benefits and
Contract Labor data on Worksheet S–3,
part V.
For the 2021 Medicare cost report
data, the majority of IPF providers did
not report data on Worksheet S–3, part
V. Two percent of freestanding IPFs and
roughly 48 percent of hospital-based
IPFs reported Employee Benefits data on
Worksheet S–3, part V. Two percent of
freestanding IPFs and roughly 13
percent of hospital-based IPFs reported
Contract Labor data on Worksheet S–3,
part V. We continue to encourage all
providers to report these data on the
Medicare cost report.
For freestanding IPFs, we proposed
that Employee Benefits cost would be
equal to the data reported on Worksheet
S–3, part V, column 2, line 2. We note
that while not required to do so,
freestanding IPFs also may report
Employee Benefits data on Worksheet
S–3, part II, which is applicable to only
IPPS providers. Similar to the method
for the 2016-based IPF market basket,
for those freestanding IPFs that report
Worksheet S–3, part II, data, but not
Worksheet S–3, part V, we proposed to
use the sum of Worksheet S–3, part II,
lines 17, 18, 20, and 22, to derive
Employee Benefits costs.
For hospital-based IPFs, we proposed
to calculate total benefit cost as the sum
of inpatient unit benefit cost, a portion
of ancillary departments benefit costs,
and a portion of overhead benefits
attributable to both the routine inpatient
unit and the ancillary departments. For
those hospital-based IPFs that report
Worksheet S–3, part V data, we
proposed inpatient unit benefit costs be
equal to Worksheet S–3, part V, column
2, line 3. Given the limited reporting on
Worksheet S–3, part V, we proposed
that for those hospital-based IPFs that
do not report these data, we calculate
inpatient unit benefits cost using a
portion of benefits cost reported for
Excluded areas on Worksheet S–3, part
II. We proposed to calculate the ratio of
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inpatient unit salaries (Worksheet A,
column 1, line 40) to total excluded area
salaries (sum of Worksheet A, column 1,
lines 20, 23, 40 through 42, 44, 45, 46,
94, 95, 98 through 101, 105 through 112,
114, 115 through 117, 190 through 194).
We then proposed to apply this ratio to
Excluded area benefits (Worksheet S–3,
part II, column 4, line 19) to derive
inpatient unit benefits cost for those
providers that do not report benefit
costs on Worksheet S–3, part V.
We proposed the ancillary
departments benefits and overhead
benefits (attributable to both the
inpatient unit and ancillary
departments) costs are derived by first
calculating the sum of hospital-based
IPF overhead salaries as described in
section IV.A.3.a.(1)(b)(i) of this final
rule, hospital-based IPF ancillary
salaries as described in section
IV.A.3.a.(1)(b)(ii) of this final rule and
hospital-based IPF overhead salaries for
ancillary cost centers as described in
section IV.A.3.a.(1)(b)(iii) of this final
rule. This sum is then multiplied by the
ratio of total facility benefits to total
facility salaries, where total facility
benefits is equal to the sum of
Worksheet S- 3, part II, column 4, lines
17–25, and total facility salaries is equal
to Worksheet S–3, part II, column 4, line
1.
(d) Contract Labor Costs
Contract Labor costs are primarily
associated with direct patient care
services. Contract labor costs for other
services such as accounting, billing, and
legal are calculated separately using
other government data sources as
described in section IV.A.3.a.(3) of this
final rule. To derive contract labor costs
using Worksheet S–3, part V, data for
freestanding IPFs, we proposed Contract
Labor costs be equal to Worksheet S–3,
part V, column 1, line 2. As we noted
for Employee Benefits, freestanding IPFs
also may report Contract Labor data on
Worksheet S–3, part II, which is
applicable to only IPPS providers. For
those freestanding IPFs that report
Worksheet S–3, part II data, but not
Worksheet S–3, part V, we proposed to
use the sum of Worksheet S–3, part II,
column 4, lines 11 and 13, to derive
Contract Labor costs.
For hospital-based IPFs, we proposed
that Contract Labor costs be equal to
Worksheet S- 3, part V, column 1, line
3. Reporting of this data continues to be
somewhat limited; therefore, we
continue to encourage all providers to
report these data on the Medicare cost
report. Given the limited reporting on
Worksheet S–3, part V, we proposed
that for those hospital-based IPFs that
do not report these data, we calculate
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Contract Labor costs using a portion of
contract labor costs reported on
Worksheet S–3, part II. We proposed to
calculate the ratio of contract labor costs
(Worksheet S–3, part II, column 4, lines
11 and 13) to PPS salaries (Worksheet
S–3, part II, column 4, line 1 less the
sum of Worksheet S–3, part II, column
4, lines 3, 401, 5, 6, 7, 701, 8, 9, 10 less
Worksheet A, column 1, line 20 and 23).
We then proposed to apply this ratio to
total inpatient routine salary costs
(Worksheet A, column 1, line 40) to
derive contract labor costs for those
providers that do not report contract
labor costs on Worksheet S–3, part V.
(e) Pharmaceuticals Costs
For freestanding IPFs, we proposed to
calculate pharmaceuticals costs using
non-salary costs reported on Worksheet
A, column 7, less Worksheet A, column
1, for the pharmacy cost center (line 15)
and drugs charged to patients cost
center (line 73).
For hospital-based IPFs, we proposed
to calculate pharmaceuticals costs as the
sum of a portion of the non-salary
pharmacy costs and a portion of the
non-salary drugs charged to patient
costs reported for the total facility. We
proposed that non-salary pharmacy
costs attributable to the hospital-based
IPF would be calculated by multiplying
total pharmacy costs attributable to the
hospital-based IPF (as reported on
Worksheet B, part I, column 15, line 40)
by the ratio of total non-salary pharmacy
costs (Worksheet A, column 2, line 15)
to total pharmacy costs (sum of
Worksheet A, columns 1 and 2 for line
15) for the total facility. We proposed
that non-salary drugs charged to patient
costs attributable to the hospital-based
IPF would be calculated by multiplying
total non-salary drugs charged to patient
costs (Worksheet B, part I, column 0,
line 73 plus Worksheet B, part I, column
15, line 73 less Worksheet A, column 1,
line 73) for the total facility by the ratio
of Medicare drugs charged to patient
ancillary costs for the IPF unit (as
reported on Worksheet D–3 for hospitalbased IPFs, column 3, line 73) to total
Medicare drugs charged to patient
ancillary costs for the total facility
(equal to the sum of Worksheet D–3,
column 3, line 73 for all relevant PPS
[that is, IPPS, IRF, IPF and SNF]).
(f) Professional Liability Insurance Costs
For freestanding and hospital-based
IPFs, we proposed that Professional
Liability Insurance (PLI) costs (often
referred to as malpractice costs) would
be equal to premiums, paid losses and
self-insurance costs reported on
Worksheet S–2, columns 1 through 3,
line 118—the same data used for the
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2016-based IPF market basket. For
hospital-based IPFs, we proposed to
assume that the PLI weight for the total
facility is similar to the hospital-based
IPF unit since the only data reported on
this worksheet is for the entire facility,
as we currently have no means to
identify the proportion of total PLI costs
that are only attributable to the hospitalbased IPF. However, when we derive
the cost weight for PLI for both hospitalbased and freestanding IPFs, we use the
total facility medical care costs as the
denominator as opposed to total
Medicare allowable costs. For
freestanding IPFs and hospital-based
IPFs, we proposed to derive total facility
medical care costs as the sum of total
costs (Worksheet B, part I, column 26,
line 202) less non-reimbursable costs
(Worksheet B, part I, column 26, lines
190 through 201). Our assumption is
that the same proportion of expenses are
used among each unit of the hospital.
(g) Home Office/Related Organization
Contract Labor Costs
For hospital-based IPFs, we proposed
to calculate the Home Office/Related
Organization Contract Labor costs using
data reported on Worksheet S–3, part II,
column 4, lines 1401, 1402, 2550, and
2551. Similar to the PLI costs, these
costs are for the entire facility.
Therefore, when we derive the cost
weight for home office/related
organization contract labor costs, we use
the total facility medical care costs as
the denominator (reflecting the total
facility costs (Worksheet B, part I,
column 26, line 202) less the
nonreimbursable costs reported on lines
190 through 201).
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(h) Capital Costs
For freestanding IPFs, we proposed
that capital costs would be equal to
Medicare allowable capital costs as
reported on Worksheet B, part II,
column 26, lines 30 through 35, 50
through 76 (excluding 52 and 75), 90
through 91, and 93.
For hospital-based IPFs, we proposed
that capital costs would be equal to IPF
inpatient capital costs (as reported on
Worksheet B, part II, column 26, line 40)
and a portion of IPF ancillary capital
costs. We calculate the portion of
ancillary capital costs attributable to the
hospital-based IPF for a given cost
center by multiplying total facility
ancillary capital costs for the specific
ancillary cost center (as reported on
Worksheet B, part II, column 26) by the
IPF ancillary ratio as described in
section IV.A.3.a.(1)(a) of this final rule.
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(2) Final Major Cost Category
Computation
After we derive costs for each of the
major cost categories and total Medicare
allowable costs for each provider using
the Medicare cost report data as
previously described, we proposed to
address data outliers using the following
steps. First, for the Wages and Salaries,
Employee Benefits, Contract Labor,
Pharmaceuticals, and Capital cost
weights, we first divide the costs for
each of these five categories by total
Medicare allowable costs calculated for
the provider to obtain cost weights for
the universe of IPF providers. We then
proposed to trim the data to remove
outliers (a standard statistical process)
by: (1) requiring that major expenses
(such as Wages and Salaries costs) and
total Medicare allowable operating costs
be greater than zero; and (2) excluding
the top and bottom 5 percent of the
major cost weight (for example, Wages
and Salaries costs as a percent of total
Medicare allowable operating costs). We
note that missing values are assumed to
be zero consistent with the methodology
for how missing values were treated in
the 2016-based IPF market basket. After
these outliers have been excluded, we
sum the costs for each category across
all remaining providers. We then divide
this by the sum of total Medicare
allowable costs across all remaining
providers to obtain a cost weight for the
2021-based IPF market basket for the
given category.
The proposed trimming methodology
for the Home Office/Related
Organization Contract Labor and PLI
cost weights are slightly different than
the proposed trimming methodology for
the other five cost categories as
described above. For these cost weights,
since we are using total facility medical
care costs rather than Medicare
allowable costs associated with IPF
services, we proposed to trim the
freestanding and hospital-based IPF cost
weights separately.
For the PLI cost weight, for each of
the providers, we first divide the PLI
costs by total facility medical care costs
to obtain a PLI cost weight for the
universe of IPF providers. We then
proposed to trim the data to remove
outliers by: (1) requiring that PLI costs
are greater than zero and are less than
total facility medical care costs; and (2)
excluding the top and bottom 5 percent
of the major cost weight trimming
freestanding and hospital-based
providers separately. After removing
these outliers, we are left with a
trimmed data set for both freestanding
and hospital-based providers. We
proposed to separately sum the costs for
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each category (freestanding and
hospital-based) across all remaining
providers. We next divide this by the
sum of total facility medical care costs
across all remaining providers to obtain
both a freestanding cost weight and
hospital-based cost weight. Lastly, we
proposed to weight these two cost
weights together using the Medicare
allowable costs from the sample of
freestanding and hospital-based IPFs
that passed the PLI trim (63 percent for
hospital-based and 37 percent for
freestanding IPFs) to derive a PLI cost
weight for the 2021-based IPF market
basket.
For the Home Office/Related
Organization Contract Labor cost
weight, for each of the providers, we
first divide the home office/related
organization contract labor costs by total
facility medical care costs to obtain a
Home Office/Related Organization
Contract Labor cost weight for the
universe of IPF providers. Similar to the
other market basket costs weights, we
proposed to trim the Home Office/
Related Organization Contract Labor
cost weight to remove outliers. Since
not all hospital-based IPFs will have
home office/related organization
contract labor costs (approximately 80
percent of hospital-based IPFs report
having a home office), we proposed to
trim the top one percent of the Home
Office/Related Organization Contract
Labor cost weight. Using this proposed
methodology, we calculate a Home
Office/Related Organization Contract
Labor cost weight for hospital-based
IPFs of 5.1 percent.
Freestanding IPFs are not required to
complete Worksheet S–3, part II.
Therefore, to estimate the Home Office/
Related Organization Contract Labor
cost weight for freestanding IPFs, we
proposed the following methodology:
Step 1: Using hospital-based IPFs
with a home office and also passing the
1 percent trim as described, we
calculate the ratio of the Home Office/
Related Organization Contract Labor
cost weight to the Medicare allowable
non-salary, non-capital cost weight
(Medicare allowable non-salary, noncapital costs as a percent of total
Medicare allowable costs).
Step 2: We identify freestanding IPFs
that report a home office on Worksheet
S–2, line 140—roughly 87 percent of
freestanding IPFs. We proposed to
calculate a Home Office/Related
Organization Contract Labor cost weight
for these freestanding IPFs by
multiplying the ratio calculated in Step
1 by the Medicare allowable non-salary,
noncapital cost weight for those
freestanding IPFs with a home office.
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Step 3: We then calculate the
freestanding IPF cost weight by
multiplying the Home Office/Related
Organization Contract Labor cost weight
in Step 2 by the total Medicare
allowable costs for freestanding IPFs
with a home office as a percent of total
Medicare allowable costs for all
freestanding IPFs (87 percent), which
derives a freestanding Home Office/
Related Organization Contract Labor
cost weight of 4.2 percent.
To calculate the overall Home Office/
Related Organization Contract Labor
cost weight for the 2021-based IPF
market basket, we proposed to weight
together the freestanding Home Office/
Related Organization Contract Labor
cost weight (4.2 percent) and the
hospital-based Home Office Contract
Labor/Related Organization cost weight
(5.1 percent) using total Medicare
allowable costs from the sample of
hospital-based IPFs that passed the one
percent trim and the universe of
freestanding IPFs. The resulting overall
cost weight for Home Office/Related
Organization Contract Labor is 4.7
percent (4.2 percent × 44 percent + 5.1
percent × 56 percent). This is the same
methodology used to calculate the
Home Office/Related Organization
Contract Labor cost weight in the 2016based IPF market basket.
Finally, we proposed to calculate the
residual ‘‘All Other’’ cost weight that
reflects all remaining costs that are not
captured in the seven cost categories
listed. See Table 1 for the resulting cost
weights for these major cost categories
that we obtain from the Medicare cost
reports.
As we did for the 2016-based IPF
market basket, we proposed to allocate
the Contract Labor cost weight to the
Wages and Salaries and Employee
Benefits cost weights based on their
relative proportions under the
assumption that contract labor costs are
comprised of both wages and salaries,
and employee benefits. The Contract
Labor allocation proportion for Wages
and Salaries is equal to the Wages and
Salaries cost weight as a percent of the
sum of the Wages and Salaries cost
weight and the Employee Benefits cost
weight. For the proposed rule, the
rounded percentage is 79 percent;
therefore, we proposed to allocate 79
percent of the Contract Labor cost
weight to the Wages and Salaries cost
weight and 21 percent to the Employee
Benefits cost weight. This allocation
was 81/19 in the 2016-based IPF market
basket (84 FR 38430). Table 2 shows the
Wages and Salaries and Employee
Benefit cost weights after Contract Labor
cost weight allocation for both the 2021based IPF market basket and 2016-based
IPF market basket.
We did not receive any comments on
our proposed methodology for
developing the major cost weights of the
2021-based IPF market basket. We are
finalizing these major cost weights as
proposed.
more detailed cost categories, we
proposed to use the 2012 Benchmark
Input-Output (I–O) ‘‘Use Tables/Before
Redefinitions/Purchaser Value’’ for
North American Industry Classification
System (NAICS) 622000, Hospitals,
published by the Bureau of Economic
Analysis (BEA). This data is publicly
available at https://www.bea.gov/
industry/io_annual.htm. For the 2016based IPF market basket, we also used
the 2012 Benchmark I–O data, the most
recent data available at the time (84 FR
38431).
The BEA Benchmark I–O data are
scheduled for publication every 5 years
with the most recent data available for
2012. The 2012 Benchmark I–O data are
derived from the 2012 Economic Census
and are the building blocks for BEA’s
economic accounts. Thus, they
represent the most comprehensive and
complete set of data on the economic
processes or mechanisms by which
(3) Derivation of the Detailed Operating
Cost Weights
To further divide the ‘‘All Other’’
residual cost weight estimated from the
2021 Medicare cost report data into
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output is produced and distributed.1
BEA also produces Annual I–O
estimates; however, while based on a
similar methodology, these estimates
reflect less comprehensive and less
detailed data sources and are subject to
revision when benchmark data becomes
available. Instead of using the less
detailed Annual I–O data, we proposed
to inflate the 2012 Benchmark I–O data
forward to 2021 by applying the annual
price changes from the respective price
proxies to the appropriate market basket
cost categories that are obtained from
the 2012 Benchmark I–O data. We
repeat this practice for each year. We
then proposed to calculate the cost
shares that each cost category represents
of the inflated 2012 data. These
resulting 2021 cost shares are applied to
the ‘‘All Other’’ residual cost weight to
obtain the detailed cost weights for the
2021-based IPF market basket. For
example, the cost for Food: Direct
Purchases represents 5.0 percent of the
sum of the ‘‘All Other’’ 2012 Benchmark
I–O Hospital Expenditures inflated to
2021; therefore, the Food: Direct
Purchases cost weight represents 5.0
percent of the proposed 2021-based IPF
market basket’s ‘‘All Other’’ cost
category (16.7 percent), yielding a
‘‘final’’ Food: Direct Purchases cost
weight of 0.8 percent in the 2021-based
IPF market basket (0.05 * 16.7 percent
= 0.8 percent).
Using this methodology, we proposed
to derive seventeen detailed IPF market
basket cost category weights from the
2021-based IPF market basket residual
cost weight (16.7 percent). These
categories are: (1) Electricity and Other
Non-Fuel Utilities; (2) Fuel: Oil and Gas;
(3) Food: Direct Purchases; (4) Food:
Contract Services; (5) Chemicals; (6)
Medical Instruments; (7) Rubber and
Plastics; (8) Paper and Printing
Products; (9) Miscellaneous Products;
(10) Professional Fees: Labor-Related;
(11) Administrative and Facilities
Support Services; (12) Installation,
Maintenance, and Repair Services; (13)
All Other Labor-Related Services; (14)
Professional Fees: Nonlabor-Related;
(15) Financial Services; (16) Telephone
Services; and (17) All Other NonlaborRelated Services.
We did not receive any comments on
our methodology to use the BEA I–O
data to derive the detailed operating
cost weights. We are finalizing this
methodology as we proposed. We note
that we did receive one comment on the
derivation of the Professional Fees:
Labor-Related cost weight, which we
1 https://www.bea.gov/papers/pdf/IOmanual_
092906.pdf.
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discuss in section IV.A.5 of this final
rule.
(4) Derivation of the Detailed Capital
Cost Weights
As described in section IV.A.3.a.(2) of
this final rule, we proposed a CapitalRelated cost weight of 7.2 percent as
obtained from the 2021 Medicare cost
reports for freestanding and hospitalbased IPF providers. We proposed to
then separate this total Capital-Related
cost weight into more detailed cost
categories.
Using 2021 Medicare cost reports, we
are able to group Capital-Related costs
into the following categories:
Depreciation, Interest, Lease, and Other
Capital-Related costs. For each of these
categories, we proposed to determine
separately for hospital-based IPFs and
freestanding IPFs what proportion of
total capital-related costs the category
represents.
For freestanding IPFs, using Medicare
Cost Report data on Worksheet A–7 part
III, we proposed to derive the
proportions for Depreciation (column 9),
Interest (column 11), Lease (column 10),
and Other Capital-related costs (column
12 through 14), which is similar to the
methodology used for the 2016-based
IPF market basket.
For hospital-based IPFs, data for these
four categories are not reported
separately for the hospital-based IPF;
therefore, we proposed to derive these
proportions using data reported on
Worksheet A–7 for the total facility. We
are assuming the cost shares for the
overall hospital are representative for
the hospital-based IPF unit. For
example, if depreciation costs make up
60 percent of total capital costs for the
entire facility, we believe it is
reasonable to assume that the hospitalbased IPF would also have a 60 percent
proportion because it is a unit contained
within the total facility. This is the same
methodology used for the 2016-based
IPF market basket (84 FR 38431).
To combine each detailed capital cost
weight for freestanding and hospitalbased IPFs into a single capital cost
weight for the 2021-based IPF market
basket, we proposed to weight together
the shares for each of the categories
(Depreciation, Interest, Lease, and Other
Capital-Related costs) based on the
share of total capital costs each provider
type represents of the total capital costs
for all IPFs for 2021. Applying this
methodology results in proportions of
total capital-related costs for
Depreciation, Interest, Lease and Other
Capital-Related costs that are
representative of the universe of IPF
providers. This is the same methodology
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used for the 2016-based IPF market
basket (84 FR 38432).
Lease costs are unique in that they are
not broken out as a separate cost
category in the 2021-based IPF market
basket. Rather, we proposed to
proportionally distribute these costs
among the cost categories of
Depreciation, Interest, and Other
Capital-Related costs, reflecting the
assumption that the underlying cost
structure of leases is similar to that of
Capital-Related costs in general. As was
done for the 2016-based IPF market
basket, we proposed to assume that 10
percent of the lease costs as a proportion
of total Capital-Related costs represent
overhead and assign those costs to the
Other Capital-Related cost category
accordingly. We proposed to distribute
the remaining lease costs proportionally
across the three cost categories
(Depreciation, Interest, and Other
Capital-Related) based on the proportion
that these categories comprise of the
sum of the Depreciation, Interest, and
Other Capital-Related cost categories
(excluding lease expenses). This would
result in three primary Capital-Related
cost categories in the 2021-based IPF
market basket: Depreciation, Interest,
and Other Capital-Related costs. This is
the same methodology used for the
2016-based IPF market basket (84 FR
38432). The allocation of these lease
expenses is shown in Table 3.
Finally, we proposed to further divide
the Depreciation and Interest cost
categories. We proposed to separate
Depreciation into the following two
categories: (1) Building and Fixed
Equipment; and (2) Movable Equipment.
We proposed to separate Interest into
the following two categories: (1)
Government/Nonprofit; and (2) Forprofit.
To disaggregate the Depreciation cost
weight, we need to determine the
percent of total Depreciation costs for
IPFs that is attributable to Building and
Fixed Equipment, which we hereafter
refer to as the ‘‘fixed percentage.’’ For
the 2021-based IPF market basket, we
proposed to use slightly different
methods to obtain the fixed percentages
for hospital-based IPFs compared to
freestanding IPFs.
For freestanding IPFs, we proposed to
use depreciation data from Worksheet
A–7 of the 2021 Medicare cost reports.
However, for hospital-based IPFs, we
determined that the fixed percentage for
the entire facility may not be
representative of the hospital-based IPF
unit due to the entire facility likely
employing more sophisticated movable
assets that are not utilized by the
hospital-based IPF. Therefore, for
hospital-based IPFs, we proposed to
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both freestanding and hospital-based
IPFs. We proposed to determine the
percent of total interest costs that are
attributed to government and nonprofit
IPFs separately for hospital-based and
freestanding IPFs. We then proposed to
weight the nonprofit percentages for
hospital-based and freestanding IPFs
together using the proportion of total
capital costs that each provider type
represents.
Table 3 provides the proposed
detailed capital cost share composition
estimated from the 2021 IPF Medicare
cost reports. These detailed capital cost
share composition percentages are
applied to the total Capital-Related cost
weight of 7.2 percent explained in detail
in sections IV.A.3.a.(1)(h) and
IV.A.3.a.(2) of this final rule.
calculate a fixed percentage using: (1)
building and fixture capital costs
allocated to the hospital-based IPF unit
as reported on Worksheet B, part I,
column 1, line 40; and (2) building and
fixture capital costs for the top five
ancillary cost centers utilized by
hospital-based IPFs accounting for 82
percent of hospital-based IPF ancillary
total costs: Clinic (Worksheet B, part I,
column 1, line 90), Drugs Charged to
Patients (Worksheet B, part I, column 1,
line 73), Emergency (Worksheet B, part
I, column 1, line 91), Laboratory
(Worksheet B, part I, column 1, line 60)
and Radiology—Diagnostic (Worksheet
B, part I, column 1, line 54). We
proposed to weight these two fixed
percentages (inpatient and ancillary)
using the proportion that each capital
cost type represents of total capital costs
in the 2021-based IPF market basket. We
proposed to then weight the fixed
percentages for hospital-based and
freestanding IPFs together using the
proportion of total capital costs each
provider type represents. For both
freestanding and hospital-based IPFs,
this is the same methodology used for
the 2016-based IPF market basket (84 FR
38432).
To disaggregate the Interest cost
weight, we determined the percent of
total interest costs for IPFs that are
attributable to government and
nonprofit facilities, which is hereafter
referred to as the ‘‘nonprofit
percentage,’’ as price pressures
associated with these types of interest
costs tend to differ from those for forprofit facilities. For the 2021-based IPF
market basket, we proposed to use
interest costs data from Worksheet A–7
of the 2021 Medicare cost reports for
BILLING CODE 4120–010–P
We did not receive any comments on
our proposed methodology for
developing the detailed capital cost
weights of the 2021-based IPF market
basket. We are finalizing these detailed
capital cost weights as proposed.
(5) 2021-Based IPF Market Basket Cost
Categories and Weights
IPF market basket compared to the
2016-based IPF market basket.
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Table 4 compares the cost categories
and weights for the finalized 2021-based
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b. Selection of Price Proxies
After developing the cost weights for
the 2021-based IPF market basket, we
proposed to select the most appropriate
wage and price proxies currently
available to represent the rate of price
change for each expenditure category.
For the majority of the cost weights, we
base the price proxies on Bureau of
Labor Statistics (BLS) data and grouped
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them into one of the following BLS
categories:
• Employment Cost Indexes (ECIs):
measure the rate of change in
employment wage rates and employer
costs for employee benefits per hour
worked. These indexes are fixed-weight
indexes and strictly measure the change
in wage rates and employee benefits per
hour. ECIs are superior to Average
Hourly Earnings (AHE) as price proxies
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for input price indexes because they are
not affected by shifts in occupation or
industry mix, and because they measure
pure price change and are available by
both occupational group and by
industry. The industry ECIs are based
on the NAICS and the occupational ECIs
are based on the Standard Occupational
Classification System (SOC).
• Producer Price Indexes (PPI):
measure the average change over time in
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the selling prices received by domestic
producers for their output. The prices
included in the PPI are from the first
commercial transaction for many
products and some services (https://
www.bls.gov/ppi/).
• Consumer Price Indexes (CPIs):
measure the average change over time in
the prices paid by urban consumers for
a market basket of consumer goods and
services (https://www.bls.gov/cpi/). CPIs
are only used when the purchases are
similar to those of retail consumers
rather than purchases at the wholesale
level, or if no appropriate PPIs are
available.
We evaluated the price proxies using
the criteria of reliability, timeliness,
availability, and relevance:
• Reliability: indicates that the index
is based on valid statistical methods and
has low sampling variability. Widely
accepted statistical methods ensure that
the data were collected and aggregated
in a way that can be replicated. Low
sampling variability is desirable because
it indicates that the sample reflects the
typical members of the population.
(Sampling variability is variation that
occurs by chance because only a sample
was surveyed rather than the entire
population.)
• Timeliness: implies that the proxy
is published regularly, preferably at
least once a quarter. The market baskets
are updated quarterly and, therefore, it
is important for the underlying price
proxies to be up-to-date, reflecting the
most recent data available. We believe
that using proxies that are published
regularly (at least quarterly, whenever
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possible) helps to ensure that we are
using the most recent data available to
update the market basket. We strive to
use publications that are disseminated
frequently, because we believe that this
is an optimal way to stay abreast of the
most current data available.
• Availability: means that the proxy is
publicly available. We prefer that our
proxies are publicly available because
this will help ensure that our market
basket updates are as transparent to the
public as possible. In addition, this
enables the public to be able to obtain
the price proxy data on a regular basis.
• Relevance: means that the proxy is
applicable and representative of the cost
category weight to which it is applied.
The CPIs, PPIs, and ECIs that we
proposed in this regulation meet these
criteria. Therefore, we believe that they
continue to be the best measure of price
changes for the cost categories to which
they would be applied.
Table 13 lists all price proxies that we
proposed to use for the 2021-based IPF
market basket. A detailed explanation of
the price proxies we proposed for each
cost category weight is provided below.
(1) Price Proxies for the Operating
Portion of the 2021-Based IPF Market
Basket
(a) Wages and Salaries
There is not a published wage proxy
that we believe represents the
occupational distribution of workers in
IPFs. To measure wage price growth in
the 2021-based IPF market basket, we
proposed to apply a proxy blend based
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on six occupational subcategories
within the Wages and Salaries category,
which would reflect the IPF
occupational mix, as was done for the
2016-based IPF market basket.
We proposed to use the National
Industry-Specific Occupational
Employment and Wage estimates for
NAICS 622200, Psychiatric & Substance
Abuse Hospitals, published by the BLS
Occupational Employment and Wage
Statistics (OEWS) program, as the data
source for the wage cost shares in the
wage proxy blend. We note that in the
spring of 2021, the Occupational
Employment Statistics (OES) program
began using the name Occupational
Employment and Wage Statistics
(OEWS) to better reflect the range of
data available from the program. Data
released on or after March 31, 2021
reflect the new program name. We
proposed to use May 2021 OEWS data.
Detailed information on the
methodology for the national industryspecific occupational employment and
wage estimates survey can be found at
https://www.bls.gov/oes/current/oes_
tec.htm. For the 2016-based IPF market
basket, we used May 2016 OES data.
Based on the OEWS data, there are six
wage subcategories: Management;
NonHealth Professional and Technical;
Health Professional and Technical;
Health Service; NonHealth Service; and
Clerical. Table 5 lists the 2021
occupational assignments for the six
wage subcategories; these are the same
occupational groups used in the 2016based IPF market basket.
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Total expenditures by occupation
(that is, occupational assignment) were
calculated by taking the OEWS number
of employees multiplied by the OEWS
annual average salary. These
expenditures were aggregated based on
the six groups in Table 5. We next
calculated the proportion of each
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group’s expenditures relative to the total
expenditures of all six groups. These
proportions, listed in Table 6, represent
the weights used in the wage proxy
blend. We then proposed to use the
published wage proxies in Table 6 for
each of the six groups (that is, wage
subcategories) as we believe these six
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price proxies are the most technically
appropriate indices available to measure
the price growth of the Wages and
Salaries cost category. These are the
same price proxies used in the 2016based IPF market basket (84 FR 38437).
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A comparison of the yearly changes
from FY 2021 to FY 2024 for the 2021based IPF wage blend and the 2016-
based IPF wage blend is shown in Table
7. The average annual growth rate is the
same for both price proxies over 2021–
2024.
(b) Employee Benefits
The benefit ECIs, listed in Table 8, are
not publicly available. Therefore, an
‘‘ECIs for Total Benefits’’ is calculated
using publicly available ‘‘ECIs for Total
Compensation’’ for each subcategory
and the relative importance of wages
within that subcategory’s total
compensation. This is the same benefits
ECI methodology that we implemented
in our 2016-based IPF market basket as
well as used in the IPPS, SNF, Home
Health Agency (HHA), IRF, LTCH, and
End-Stage Renal Disease (ESRD) market
baskets. We believe that the six price
proxies listed in Table 8 are the most
technically appropriate indices to
measure the price growth of the
Employee Benefits cost category in the
2021-based IPF market basket.
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To measure benefits price growth in
the 2021-based IPF market basket, we
proposed to apply a benefits proxy
blend based on the same six
subcategories and the same six blend
weights for the wage proxy blend. These
subcategories and blend weights are
listed in Table 8.
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A comparison of the yearly changes
from FY 2021 to FY 2024 for the 2021based IPF benefit proxy blend and the
2016-based IPF benefit proxy is shown
in Table 9. The average annual growth
rate is the same for both price proxies
over 2021 through 2024.
(c) Electricity and Other Non-Fuel
Utilities
data (use table before redefinitions,
purchaser’s value for NAICS 622000
[Hospitals]), shows that Petroleum
Refineries expenses account for
approximately 90 percent and Natural
Gas expenses account for approximately
10 percent of Hospitals’ (NAICS 622000)
total Fuel: Oil and Gas expenses.
Therefore, we proposed to use a blend
of 90 percent of the PPI for Petroleum
Refineries (BLS series code
PCU324110324110) and 10 percent of
the PPI Commodity Index for Natural
Gas (BLS series code WPU0531) as the
price proxy for this cost category. This
is the same blend that was used for the
2016-based IPF market basket (84 FR
38438).
(e) Professional Liability Insurance
(d) Fuel: Oil and Gas
Similar to the 2016-based IPF market
basket, for the 2021-based IPF market
basket, we proposed to use a blend of
the PPI for Petroleum Refineries and the
PPI Commodity for Natural Gas. Our
analysis of the Bureau of Economic
Analysis’ 2012 Benchmark Input-Output
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We proposed to use the CMS Hospital
Professional Liability Index to measure
changes in PLI premiums. To generate
this index, we collect commercial
insurance premiums for a fixed level of
coverage while holding non-price
factors constant (such as a change in the
level of coverage). This is the same
proxy used in the 2016-based IPF
market basket (84 FR 38438).
(f) Pharmaceuticals
We proposed to use the PPI for
Pharmaceuticals for Human Use,
Prescription (BLS series code
WPUSI07003) to measure the price
growth of this cost category. This is the
same proxy used in the 2016-based IPF
market basket (84 FR 38438).
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We proposed to use the PPI
Commodity Index for Commercial
Electric Power (BLS series code
WPU0542) to measure the price growth
of this cost category (which we
proposed to rename from Electricity to
Electricity and Other Non-Fuel
Utilities). This is the same price proxy
used in the 2016-based IPF market
basket (84 FR 38438).
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(j) Medical Instruments
We proposed to use a blended price
proxy for the Medical Instruments
category, as shown in Table 11. The
2012 Benchmark I–O data shows the
majority of medical instruments and
supply costs are for NAICS 339112—
Surgical and medical instrument
manufacturing costs (approximately 56
percent) and NAICS 339113—Surgical
appliance and supplies manufacturing
costs (approximately 43 percent).
Therefore, we proposed to use a blend
of these two price proxies. To proxy the
price changes associated with NAICS
339112, we proposed to use the PPI for
Surgical and medical instruments (BLS
series code WPU1562). This is the same
price proxy we used in the 2016-based
IPF market basket. To proxy the price
changes associated with NAICS 339113,
we proposed to use a 50/50 blend of the
PPI for Medical and surgical appliances
and supplies (BLS series code
WPU1563) and the PPI for
Miscellaneous products, Personal safety
equipment and clothing (BLS series
code WPU1571). We proposed to
include the latter price proxy as it will
reflect personal protective equipment
including but not limited to face shields
and protective clothing. The 2012
Benchmark I–O data does not provide
specific expenses for these products;
however, we recognize that this category
reflects costs faced by IPFs.
(k) Rubber and Plastics
category. This is the same proxy used in
the 2016-based IPF market basket (84 FR
38439).
(n) Professional Fees: Labor-Related
We proposed to use the PPI for
Rubber and Plastic Products (BLS series
code WPU07) to measure price growth
of this cost category. This is the same
proxy used in the 2016-based IPF
market basket (84 FR 38439).
(l) Paper and Printing Products
We proposed to use the PPI for
Converted Paper and Paperboard
Products (BLS series code WPU0915) to
measure the price growth of this cost
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(i) Chemicals
(m) Miscellaneous Products
We proposed to use the PPI for
Finished Goods Less Food and Energy
(BLS series code WPUFD4131) to
measure the price growth of this cost
category. This is the same proxy used in
the 2016-based IPF market basket (84 FR
38439).
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We proposed to use the ECI for Total
Compensation for Private Industry
workers in Professional and Related
(BLS series code CIU2010000120000I) to
measure the price growth of this
category. This is the same proxy used in
the 2016-based IPF market basket (84 FR
38439).
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(h) Food: Contract Purchases
We proposed to use the CPI for Food
Away From Home (BLS series code
CUUR0000SEFV) to measure the price
growth of this cost category. This is the
same proxy used in the 2016-based IPF
market basket (84 FR 38438).
Similar to the 2016-based IPF market
basket, we proposed to use a four-part
blended PPI as the proxy for the
chemical cost category in the 2021based IPF market basket. The proposed
blend is composed of the PPI for
Industrial Gas Manufacturing, Primary
Products (BLS series code
PCU325120325120P), the PPI for Other
Basic Inorganic Chemical
Manufacturing (BLS series code
PCU32518–32518-), the PPI for Other
Basic Organic Chemical Manufacturing
(BLS series code PCU32519–32519-),
and the PPI for Other Miscellaneous
Chemical Product Manufacturing (BLS
series code PCU325998325998). For the
2021-based IPF market basket, we
proposed to derive the weights for the
PPIs using the 2012 Benchmark I–O
data.
Table 10 shows the weights for each
of the four PPIs used to create the
blended Chemical proxy for the 2021based IPF market basket. This is the
same blend that was used for the 2016based IPF market basket (84 FR 38439).
(g) Food: Direct Purchases
We proposed to use the PPI for
Processed Foods and Feeds (BLS series
code WPU02) to measure the price
growth of this cost category. This is the
same proxy used in the 2016-based IPF
market basket (84 FR 38438).
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(o) Administrative and Facilities
Support Services
We proposed to use the ECI for Total
Compensation for Private Industry
workers in Office and Administrative
Support (BLS series code
CIU2010000220000I) to measure the
price growth of this category. This is the
same proxy used in the 2016-based IPF
market basket (84 FR 38439).
(p) Installation, Maintenance, and
Repair Services
We proposed to use the ECI for Total
Compensation for Civilian workers in
Installation, Maintenance, and Repair
(BLS series code CIU1010000430000I) to
measure the price growth of this cost
category. This is the same proxy used in
the 2016-based IPF market basket (84 FR
38439).
(q) All Other: Labor-Related Services
We proposed to use the ECI for Total
Compensation for Private Industry
workers in Service Occupations (BLS
series code CIU2010000300000I) to
measure the price growth of this cost
category. This is the same proxy used in
the 2016-based IPF market basket (84 FR
38439).
(r) Professional Fees: Nonlabor-Related
We proposed to use the ECI for Total
Compensation for Private Industry
workers in Professional and Related
(BLS series code CIU2010000120000I) to
measure the price growth of this
category. This is the same proxy used in
the 2016-based IPF market basket (84 FR
38439).
(s) Financial Services
We proposed to use the ECI for Total
Compensation for Private Industry
workers in Financial Activities (BLS
series code CIU201520A000000I) to
measure the price growth of this cost
category. This is the same proxy used in
the 2016-based IPF market basket (84 FR
38439).
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(t) Telephone Services
We proposed to use the CPI for
Telephone Services (BLS series code
CUUR0000SEED) to measure the price
growth of this cost category. This is the
same proxy used in the 2016-based IPF
market basket (84 FR 38439).
(u) All Other: Nonlabor-Related Services
We proposed to use the CPI for All
Items Less Food and Energy (BLS series
code CUUR0000SA0L1E) to measure the
price growth of this cost category. This
is the same proxy used in the 2016based IPF market basket (84 FR 38439).
We did not receive any comments on
our proposed price proxies for the
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operating portion of the 2021-based IPF
market basket. We are finalizing these
price proxies as proposed.
Table 13 lists all price proxies that we
are finalizing for the 2021-based IPF
market basket.
(2) Price Proxies for the Capital Portion
of the 2021-Based IPF Market Basket
(a) Capital Price Proxies Prior to Vintage
Weighting
We proposed to use the same price
proxies for the capital-related cost
categories in the 2021-based IPF market
basket as were used in the 2016-based
IPF market basket, which are provided
in Table 13 and described below.
Specifically, we proposed to proxy:
• Depreciation: Building and Fixed
Equipment cost category by BEA’s
Chained Price Index for Nonresidential
Construction for Hospitals and Special
Care Facilities (BEA Table 5.4.4. Price
Indexes for Private Fixed Investment in
Structures by Type).
• Depreciation: Movable Equipment
cost category by the PPI for Machinery
and Equipment (BLS series code
WPU11).
• Nonprofit Interest cost category by
the average yield on domestic municipal
bonds (Bond Buyer 20-bond index).
• For-profit Interest cost category by
the iBoxx AAA Corporate Bond Yield
index
• Other Capital-Related cost category
by the CPI–U for Rent of Primary
Residence (BLS series code
CUUS0000SEHA).
We believe these are the most
appropriate proxies for IPF capitalrelated costs that meet our selection
criteria of relevance, timeliness,
availability, and reliability. We also
proposed to vintage weight the capital
price proxies for Depreciation and
Interest to capture the long-term
consumption of capital. This vintage
weighting method is similar to the
method used for the 2016-based IPF
market basket (84 FR 38440) and is
described below.
(b) Vintage Weights for Price Proxies
Because capital is acquired and paid
for over time, capital-related expenses
in any given year are determined by
both past and present purchases of
physical and financial capital. The
vintage-weighted capital-related portion
of the 2021-based IPF market basket is
intended to capture the long-term
consumption of capital, using vintage
weights for depreciation (physical
capital) and interest (financial capital).
These vintage weights reflect the
proportion of capital-related purchases
attributable to each year of the expected
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life of building and fixed equipment,
movable equipment, and interest. We
proposed to use vintage weights to
compute vintage-weighted price
changes associated with depreciation
and interest expenses.
Capital-related costs are inherently
complicated and are determined by
complex capital-related purchasing
decisions, over time, based on such
factors as interest rates and debt
financing. In addition, capital is
depreciated over time instead of being
consumed in the same period it is
purchased. By accounting for the
vintage nature of capital, we are able to
provide an accurate and stable annual
measure of price changes. Annual nonvintage price changes for capital are
unstable due to the volatility of interest
rate changes, and therefore, do not
reflect the actual annual price changes
for IPF capital-related costs. The capitalrelated component of the 2021-based
IPF market basket reflects the
underlying stability of the capitalrelated acquisition process.
The methodology used to calculate
the vintage weights for the 2021-based
IPF market basket is the same as that
used for the 2016-based IPF market
basket (84 FR 38439 through 38441)
with the only difference being the
inclusion of more recent data. To
calculate the vintage weights for
depreciation and interest expenses, we
first need a time series of capital-related
purchases for building and fixed
equipment and movable equipment. We
found no single source that provides an
appropriate time series of capital-related
purchases by hospitals for all of the
above components of capital purchases.
The early Medicare cost reports did not
have sufficient capital-related data to
meet this need. Data we obtained from
the American Hospital Association
(AHA) do not include annual capitalrelated purchases. However, we are able
to obtain data on total expenses back to
1963 from the AHA. Consequently, we
proposed to use data from the AHA
Panel Survey and the AHA Annual
Survey to obtain a time series of total
expenses for hospitals. We then
proposed to use data from the AHA
Panel Survey supplemented with the
ratio of depreciation to total hospital
expenses obtained from the Medicare
cost reports to derive a trend of annual
depreciation expenses for 1963 through
2020, which is the latest year of AHA
data available. We proposed to separate
these depreciation expenses into annual
amounts of building and fixed
equipment depreciation and movable
equipment depreciation as determined
earlier. From these annual depreciation
amounts, we derive annual end-of-year
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book values for building and fixed
equipment and movable equipment
using the expected life for each type of
asset category. While data is not
available that is specific to IPFs, we
believe this information for all hospitals
serves as a reasonable alternative for the
pattern of depreciation for IPFs.
To continue to calculate the vintage
weights for depreciation and interest
expenses, we also need to account for
the expected lives for Building and
Fixed Equipment, Movable Equipment,
and Interest for the 2021-based IPF
market basket. We proposed to calculate
the expected lives using Medicare cost
report data from freestanding and
hospital-based IPFs. The expected life of
any asset can be determined by dividing
the value of the asset (excluding fully
depreciated assets) by its current year
depreciation amount. This calculation
yields the estimated expected life of an
asset if the rates of depreciation were to
continue at current year levels,
assuming straight-line depreciation. We
proposed to determine the expected life
of building and fixed equipment
separately for hospital-based IPFs and
freestanding IPFs, and then weight these
expected lives using the percent of total
capital costs each provider type
represents. We proposed to apply a
similar method for movable equipment.
Using these proposed methods, we
determined the average expected life of
building and fixed equipment to be
equal to 25 years, and the average
expected life of movable equipment to
be equal to 12 years. For the expected
life of interest, we believe vintage
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weights for interest should represent the
average expected life of building and
fixed equipment because, based on
previous research described in the FY
1997 IPPS final rule (61 FR 46198), the
expected life of hospital debt
instruments and the expected life of
buildings and fixed equipment are
similar. We note that for the 2016-based
IPF market basket, the expected life of
building and fixed equipment is 22
years, and the expected life of movable
equipment is 11 years (84 FR 38441).
Multiplying these expected lives by
the annual depreciation amounts results
in annual year-end asset costs for
building and fixed equipment and
movable equipment. We then calculate
a time series, beginning in 1964, of
annual capital purchases by subtracting
the previous year’s asset costs from the
current year’s asset costs.
For the building and fixed equipment
and movable equipment vintage
weights, we proposed to use the real
annual capital-related purchase
amounts for each asset type to capture
the actual amount of the physical
acquisition, net of the effect of price
inflation. These real annual capitalrelated purchase amounts are produced
by deflating the nominal annual
purchase amount by the associated price
proxy as provided earlier in this final
rule. For the interest vintage weights,
we proposed to use the total nominal
annual capital-related purchase
amounts to capture the value of the debt
instrument (including, but not limited
to, mortgages and bonds). Using these
capital-related purchase time series
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specific to each asset type, we proposed
to calculate the vintage weights for
building and fixed equipment, for
movable equipment, and for interest.
The vintage weights for each asset
type are deemed to represent the
average purchase pattern of the asset
over its expected life (in the case of
building and fixed equipment and
interest, 25 years, and in the case of
movable equipment, 12 years). For each
asset type, we used the time series of
annual capital-related purchase
amounts available from 2020 back to
1964. These data allow us to derive
thirty-three 25-year periods of capitalrelated purchases for building and fixed
equipment and interest, and forty-six
12-year periods of capital-related
purchases for movable equipment. For
each 25-year period for building and
fixed equipment and interest, or 12-year
period for movable equipment, we
calculate annual vintage weights by
dividing the capital-related purchase
amount in any given year by the total
amount of purchases over the entire 25year or 12-year period. This calculation
is done for each year in the 25-year or
12-year period and for each of the
periods for which we have data. We
then calculate the average vintage
weight for a given year of the expected
life by taking the average of these
vintage weights across the multiple
periods of data. The vintage weights for
the capital-related portion of the 2021based IPF market basket and the 2016based IPF market basket are presented
in Table 12.
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The process of creating vintageweighted price proxies requires
applying the vintage weights to the
price proxy index where the last applied
vintage weight in Table 12 is applied to
the most recent data point. We have
provided on the CMS website an
example of how the vintage weighting
price proxies are calculated, using
example vintage weights and example
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price indices. The example can be found
at https://www.cms.gov/ResearchStatistics-Data-and-Systems/StatisticsTrends-and-Reports/
MedicareProgramRatesStats/
MarketBasketResearch.html in the zip
file titled ‘‘Weight Calculations as
described in the IPPS FY 2010 Proposed
Rule.’’
We did not receive any comments on
our proposed price proxies for the
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capital portion of the 2021-based IPF
market basket. We are finalizing these
price proxies as proposed.
(3) Summary of Price Proxies of the
2021-Based IPF Market Basket
Table 13 shows both the operating
and capital price proxies that we are
finalizing for the 2021-based IPF market
basket.
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After consideration of public
comments, we are finalizing the 2021based IPF market basket as proposed.
4. FY 2024 Market Basket Update and
Productivity Adjustment
a. FY 2024 Market Basket Update
For FY 2024 (that is, beginning
October 1, 2023 and ending September
30, 2024), we proposed to use an
estimate of the proposed 2021-based IPF
market basket increase factor to update
the IPF PPS base payment rate.
Consistent with historical practice, we
estimate the market basket update for
the IPF PPS based on IHS Global Inc.’s
(IGI) forecast. IGI is a nationally
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b. Productivity Adjustment
Section 1886(s)(2)(A)(i) of the Act
requires the application of the
productivity adjustment described in
section 1886(b)(3)(B)(xi)(II) of the Act to
the IPF PPS for the RY beginning in
2012 (that is, a RY that coincides with
a FY) and each subsequent RY. The
statute defines the productivity
adjustment to be equal to the 10-year
moving average of changes in annual
economy-wide, private nonfarm
business multifactor productivity (as
projected by the Secretary for the 10year period ending with the applicable
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recognized economic and financial
forecasting firm with which CMS
contracts to forecast the components of
the market baskets.
Using IGI’s fourth quarter 2022
forecast with historical data through the
third quarter of 2022, the projected
proposed 2021-based IPF market basket
increase factor for FY 2024 was 3.2
percent. We also proposed that if more
recent data were subsequently available
(for example, a more recent estimate of
the market basket increase factor) we
would use such data, to determine the
FY 2024 update in the final rule.
Based on IGI’s second quarter 2023
forecast with historical data through the
first quarter of 2023, the 2021-based IPF
market basket increase percentage for
FY 2024 is 3.5 percent. For comparison,
the current 2016-based IPF market
basket is also projected to increase by
3.5 percent in FY 2024 based on IGI’s
second quarter 2023 forecast. Table 14
compares the 2021-based IPF market
basket and the 2016-based IPF market
basket percent changes. On average, the
two indexes produce similar updates to
one another, with the 4-year average
historical growth rates (for FY 2019–FY
2022) of the 2021-based IPF market
basket being equal to 3.2 percent
compared to the 2016-based IPF market
basket with 3.2 percent.
FY, year, cost reporting period, or other
annual period) (the ‘‘productivity
adjustment’’). The United States
Department of Labor’s Bureau of Labor
Statistics (BLS) publishes the official
measures of productivity for the United
States economy. We note that
previously the productivity measure
referenced in section
1886(b)(3)(B)(xi)(II) of the Act, was
published by BLS as private nonfarm
business multifactor productivity.
Beginning with the November 18, 2021
release of productivity data, BLS
replaced the term multifactor
productivity (MFP) with total factor
productivity (TFP). BLS noted that this
is a change in terminology only and will
not affect the data or methodology. As
a result of the BLS name change, the
productivity measure referenced in
section 1886(b)(3)(B)(xi)(II) of the Act is
now published by BLS as private
nonfarm business total factor
productivity. However, as mentioned
above, the data and methods are
unchanged. We refer readers to
www.bls.gov for the BLS historical
published TFP data. A complete
description of IGI’s TFP projection
methodology is available on the CMS
website at https://www.cms.gov/
research-statistics-data-and-systems/
statistics-trends-and-reports/
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medicareprogramratesstats/
marketbasketresearch. In addition, in
the FY 2022 IPF PPS final rule (86 FR
42611), we noted that effective with FY
2022 and forward, CMS changed the
name of this adjustment to refer to it as
the productivity adjustment rather than
the MFP adjustment.
Using IGI’s fourth quarter 2022
forecast, the 10-year moving average
growth of TFP for FY 2024 was
projected to be 0.2 percent. Thus, in
accordance with section 1886(s)(2)(A)(i)
of the Act, we proposed to calculate the
FY 2024 market basket update, which is
used to determine the applicable
percentage increase for the IPF
payments, using IGI’s fourth quarter
2022 forecast of the proposed 2021based IPF market basket. We proposed
to then reduce this percentage increase
by the estimated productivity
adjustment for FY 2024 of 0.2
percentage point (the 10-year moving
average growth of TFP for the period
ending FY 2024 based on IGI’s fourth
quarter 2022 forecast). Therefore, the
proposed FY 2024 IPF update was equal
to 3.0 percent (3.2 percent market basket
update reduced by the 0.2 percentage
point productivity adjustment).
Furthermore, we proposed that if more
recent data became available after the
publication of the proposed rule and
before the publication of the final rule
(for example, a more recent estimate of
the productivity adjustment), we would
use such data, if appropriate, to
determine the FY 2024 productivity
adjustment in the final rule.
Using IGI’s second quarter 2023
forecast, the 10-year moving average
growth of TFP for FY 2024 is projected
to be 0.2 percent. Thus, in accordance
with section 1886(s)(2)(A)(i) of the Act,
we calculate the FY 2024 market basket
update, which is used to determine the
applicable percentage increase for the
IPF payments, using IGI’s second
quarter 2023 forecast of the 2021-based
IPF market basket. We then reduce this
percentage increase by the estimated
productivity adjustment for FY 2024 of
0.2 percentage point (the 10-year
moving average growth of TFP for the
period ending FY 2024 based on IGI’s
second quarter 2023 forecast).
Therefore, the FY 2024 IPF update is
equal to 3.3 percent (3.5 percent market
basket update reduced by the 0.2
percentage point productivity
adjustment).
We invited public comment on our
proposals for the FY 2024 market basket
update and productivity adjustment.
The following is a summary of the
public comments received on the
proposed FY 2024 market basket update
and productivity adjustment.
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Comment: Several commenters
expressed concern about the proposed
2021-based IPF market basket increase
factor for FY 2024 of 3.2 percent. They
stated that hospitals throughout the
country face enormous cost pressures,
with labor costs (due to increased
demand and workforce shortages)
leading to this dramatic increase in
overall cost pressure. They also noted
the significant cost increases for drugs,
medical supplies, and personal
protective equipment since before the
PHE. The commenters stated that the
cumulative effect of this inflationary
pressure coupled with the proposed low
Medicare payment increases for FY
2024 will continue to have negative
effects on IPF operating margins. They
cited that the Medicare Payment
Advisory Commission determined that
Medicare has failed to cover the cost of
caring for patients in hospital-based and
freestanding nonprofit IPFs since at
least 2016.
The commenters also noted that CMS
proposed that if more recent data
became available after the publication of
the proposed rule and before the
publication of the final rule that CMS
would use such data to determine the
FY 2024 update in the final rule. They
recommended CMS use more recent
data and implement a payment rate for
FY 2024 that more accurately reflects
current costs, rather than relying on data
that preceded the extraordinary
inflation they are experiencing. Some
commenters suggested CMS use other
methods to determine the market basket
update, such as the average growth rate
in allowable Medicare costs per riskadjusted discharge for IPFs between FY
2019 and FY 2021 to calculate the FY
2024 final rule market basket update.
They stated that if CMS fails to provide
an adequate market basket update, they
are deeply concerned inadequate
payments will result in reduced access
to inpatient psychiatric services for
Medicare beneficiaries.
Response: We appreciate the
commenters’ concerns regarding
inflationary pressure facing IPFs and the
proposed FY 2024 market basket
update. As stated in Section IV.A.2 in
this final rule, the IPF market basket
(including the proposed 2021-based and
other CMS market baskets) is a fixedweight, Laspeyres-type index that
measures price changes over time. Since
the inception of the IPF PPS, the IPF
payment rates (with the exception of
statutorily mandated updates) have been
updated by a projection of a market
basket percentage increase, which is
designed to measure price inflation for
IPF providers and does not reflect
increases in costs associated with
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changes in the volume or intensity of
input goods and services (such as the
quantity of labor used). In this way, the
IPF market basket is consistent in
concept and methodology with market
baskets used for other CMS PPS
updates, including IPPS, SNF, and
HHA. The longstanding IPF market
basket methodology establishes a market
basket that appropriately reflects
expectations, based on the latest
available data, of price inflation for IPF
providers for FY 2024. It would be
inappropriate for the IPF market basket
to reflect the method proposed by the
commenter where the update would be
based on increases in Medicare
allowable costs per risk-adjusted
discharge from a past period, since that
measure would incorporate changes in
costs that are not solely reflective of
price inflation that is intended to be
captured by the market basket update in
the IPF PPS.
The projection of the 2021-based IPF
market basket is based on the most
recent forecast from IHS Global Inc.—a
nationally recognized economic and
financial forecasting firm with which
CMS contracts to forecast the price
proxies of the market baskets. For this
final rule, based on the more recent IGI
second quarter 2023 forecast with
historical data through the first quarter
of 2023, the projected 2021-based IPF
market basket increase factor for FY
2024 is 3.5 percent, which is 0.3
percentage point higher than the
projected FY 2024 market basket
increase factor in the proposed rule, and
reflects an increase in compensation
prices of 4.0 percent. We note that the
10-year historical average (2013–2022)
growth rate of the 2021-based IPF
market basket is 2.4 percent with an
average growth rate in compensation
prices of 2.5 percent.
Therefore, consistent with our
historical practice of estimating market
basket increases based on the best
available data, we are finalizing a
market basket increase percentage of 3.5
percent for FY 2024.
Comment: Several commenters
expressed concern about the application
of the productivity adjustment, stating
that the PHE has had unimaginable
impacts on hospital productivity. They
state that even before the PHE, OACT
indicated that hospital productivity will
be less than the general economy-wide
productivity, which is the measure that
is required by law to be used to derive
the productivity adjustment. Given that
CMS is required by statute to implement
a productivity adjustment to the market
basket update, commenters asked the
agency to work with the Congress to
permanently eliminate this unjustified
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reduction to hospital payments. Further,
they asked CMS to use its authority
under section 1886(s) of the Act to
remove the productivity adjustment for
any fiscal year that was covered under
PHE determination (that is, 2020 (0.4
percent), 2021 (0.0 percent), 2022 (0.7
percent), and 2023 (0.3 percent)) from
the calculation of the market basket
update for FY 2024 and any year
thereafter.
Response: Section 1886(s)(2)(A)(i) of
the Act requires the application of the
productivity adjustment described in
section 1886(b)(3)(xi)(II) of the Act. As
required by statute, the FY 2024
productivity adjustment is derived
based on the 10-year moving average
growth in economy-wide productivity
for the period ending FY 2024. We
recognize the concerns of the
commenters regarding the
appropriateness of the productivity
adjustment; however, we are required
pursuant to section 1886(s)(2)(A)(i) of
the Act to apply the specific
productivity adjustment described here.
Because that provision specifically
requires application of the productivity
adjustment, we do not believe section
1886(s) of the Act permits the Secretary
discretion to remove it from the
calculation of the market basket update.
Comment: Commenters noted that
CMS has underestimated the IPF market
basket increase over the last several
years. They encouraged CMS to utilize
its exceptions and adjustments authority
to apply a one-time adjustment to
course correct for its significantly lower
estimates of costs for FYs 2021 through
2023. They stated that failing to correct
CMS’s gross underestimation of the
payment updates during the pandemic
will further perpetuate inaccuracies in
the payment rate moving forward,
resulting in a permanent cut to IPF
payments.
Response: The IPF market basket
updates are set prospectively, which
means that the update relies on a mix
of both historical data for part of the
period for which the update is
calculated and forecasted data for the
remainder. For instance, the FY 2024
market basket update in this final rule
reflects historical data through the first
quarter of CY 2023 and forecasted data
through the third quarter of CY 2024.
While there is no precedent to adjust for
market basket forecast error in the IPF
payment update, a forecast error can be
calculated by comparing the actual
market basket increase for a given year
less the forecasted market basket
increase. Due to the uncertainty
regarding future price trends, forecast
errors can be both positive and negative.
Regarding the comment that the IPF
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market basket increase over the last
several years has been underestimated,
we disagree with this assertion, as from
2012 through 2020, the forecasted
market basket updates for each payment
year for IPFs were higher than the actual
market basket updates. For this final
rule, we have incorporated more recent
historical data and forecasts to capture
the price and wage pressures facing
IPFs. We believe IGI’s second quarter
2023 forecast of the FY 2024 percentage
increase in the 2021-based IPF market
basket is the best available projection of
inflation to determine the applicable
percentage increase for the IPF
payments in FY 2024.
Final Decision: After consideration of
public comments, we are finalizing a FY
2024 IPF payment rate update of 3.3
percent (3.5 percent IPF market basket
percentage increase reduced by the 0.2
percentage point productivity
adjustment).
5. Labor-Related Share for FY 2024
Due to variations in geographic wage
levels and other labor-related costs, we
believe that payment rates under the IPF
PPS should continue to be adjusted by
a geographic wage index, which applies
to the labor-related portion of the
Federal per diem base rate (hereafter
referred to as the labor-related share).
The labor-related share is determined by
identifying the national average
proportion of total costs that are related
to, influenced by, or vary with the local
labor market. We proposed to continue
to classify a cost category as laborrelated if the costs are labor-intensive
and vary with the local labor market.
We proposed to include in the laborrelated share the sum of the relative
importance of the following cost
categories: Wages and Salaries,
Employee Benefits, Professional Fees:
Labor-Related, Administrative and
Facilities Support Services, Installation,
Maintenance, and Repair Services, All
Other: Labor-Related Services, and a
portion of the Capital-Related cost
weight from the 2021-based IPF market
basket. These are the same categories as
the 2016-based IPF market basket.
Similar to the 2016-based IPF market
basket, the 2021-based IPF market
basket includes two cost categories for
nonmedical Professional fees (including
but not limited to, expenses for legal,
accounting, and engineering services).
These are Professional Fees: LaborRelated and Professional Fees:
Nonlabor-Related. For the 2021-based
IPF market basket, we proposed to
estimate the labor-related percentage of
non-medical professional fees (and
assign these expenses to the
Professional Fees: Labor-Related
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services cost category) based on the
same method that was used to
determine the labor-related percentage
of professional fees in the 2016-based
IPF market basket.
As was done in the 2016-based IPF
market basket, we proposed to
determine the proportion of legal,
accounting and auditing, engineering,
and management consulting services
that meet our definition of labor-related
services based on a survey of hospitals
conducted by CMS in 2008. We notified
the public of our intent to conduct this
survey on December 9, 2005, (70 FR
73250) and did not receive any public
comments in response to the notice (71
FR 8588). A discussion of the
composition of the survey and poststratification can be found in the FY
2010 IPPS/LTCH PPS final rule (74 FR
43850 through 43856). Based on the
weighted results of the survey, we
determined that hospitals purchase, on
average, the following portions of
contracted professional services outside
of their local labor market:
• 34 percent of accounting and
auditing services.
• 30 percent of engineering services.
• 33 percent of legal services.
• 42 percent of management
consulting services.
We proposed to apply each of these
percentages to the respective 2012
Benchmark I–O cost category
underlying the professional fees cost
category to determine the Professional
Fees: Nonlabor-Related costs. The
Professional Fees: Labor-Related costs
were determined to be the difference
between the total costs for each
Benchmark I–O category and the
Professional Fees: Nonlabor-Related
costs. This is the same methodology that
we used to separate the 2016-based IPF
market basket professional fees category
into Professional Fees: Labor-Related
and Professional Fees: Nonlabor-Related
cost categories (84 FR 38445).
Effective for transmittal 18, (https://
www.cms.gov/Regulations-andGuidance/Guidance/Transmittals/
Transmittals/r18p240i) the hospital
Medicare cost report (CMS Form 2552–
10, OMB No. 0938–0050) is collecting
information on whether a hospital
purchased professional services (for
example, legal, accounting, tax
preparation, bookkeeping, payroll,
advertising, and/or management/
consulting services) from an unrelated
organization and if the majority of these
expenses were purchased from
unrelated organizations located outside
of the main hospital’s local area labor
market. We encourage all providers to
provide this information so we can
potentially use these data in future
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rulemaking to determine the laborrelated share.
In the 2021-based IPF market basket,
nonmedical professional fees that were
subject to allocation based on these
survey results represent 3.3 percent of
total costs (and are limited to those fees
related to Accounting & Auditing, Legal,
Engineering, and Management
Consulting services). Based on our
survey results, we proposed to
apportion 2.1 percentage points of the
3.3 percentage point figure into the
Professional Fees: Labor-Related share
cost category and designate the
remaining 1.2 percentage point into the
Professional Fees: Nonlabor-Related cost
category.
In addition to the professional
services listed, for the 2021-based IPF
market basket, we proposed to allocate
a proportion of the Home Office/Related
Organization Contract Labor cost
weight, calculated using the Medicare
cost reports, into the Professional Fees:
Labor-Related and Professional Fees:
Nonlabor-Related cost categories. We
proposed to classify these expenses as
labor-related and nonlabor-related, as
many facilities are not located in the
same geographic area as their home
office and, therefore, do not meet our
definition for the labor-related share,
which requires the services to be
purchased in the local labor market.
Similar to the 2016-based IPF market
basket, we proposed for the 2021-based
IPF market basket to use the Medicare
cost reports for both freestanding IPF
providers and hospital-based IPF
providers to determine the home office
labor-related percentages. The Medicare
cost report requires a hospital to report
information regarding its home office
provider. Using information on the
Medicare cost report, we then compare
the location of the IPF with the location
of the IPF’s home office. We proposed
to classify an IPF with a home office
located in its respective labor market if
the IPF and its home office are located
in the same metropolitan statistical area
(MSA). We then determine the
proportion of the Home Office/Related
Organization Contract Labor cost weight
that should be allocated to the laborrelated share based on the percent of
total Medicare allowable costs for those
IPFs that had home offices located in
their respective local labor markets of
total Medicare allowable costs for IPFs
with a home office. We determined an
IPF’s and its home office’s MSA using
their zip code information from the
Medicare cost report. Using this
methodology, we determined that 46
percent of IPFs’ Medicare allowable
costs were for home offices located in
their respective local labor markets.
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Therefore, we are allocating 46 percent
of the Home Office/Related
Organization Contract Labor cost weight
(2.1 percentage points = 4.7 percent
times 46 percent) to the Professional
Fees: Labor-Related cost weight and 54
percent of the Home Office/Related
Organization Contract Labor cost weight
to the Professional Fees: NonlaborRelated cost weight (2.5 percentage
points = 4.7 percent times 54 percent).
The same methodology was used for the
2016-based IPF market basket (84 FR
38445).
In summary, we apportioned 2.1
percentage points of the non-medical
professional fees and 2.1 percentage
points of the Home Office/Related
Organization Contract Labor cost weight
into the Professional Fees: LaborRelated cost category. This amount was
added to the portion of professional fees
that we already identified as laborrelated using the I–O data such as
contracted advertising and marketing
costs (approximately 0.5 percentage
point of total costs), resulting in a
Professional Fees: Labor-Related cost
weight of 4.7 percent.
Comment: One commenter
appreciated CMS’s proposal to increase
the labor-related share based on data
that better reflects increased labor costs
as a percentage of an IPF’s overall cost
structure. However, they disagreed with
CMS’s proposal to exclude from the
labor-related share the proportion of
non-medical professional services fees
presumed to have been purchased
outside of the hospital’s labor market.
The commenter disagreed with CMS’s
assertion/assumption that services
purchased from national firms are not
affected by the local labor market. The
commenter stated that when hospitals
seek professional services, the services
they are seeking (such as, accounting,
engineering, or management consulting)
typically are not so unique that they
could only be provided by regional or
national firms. The commenter stated
that CMS’s own survey data support this
conclusion, as approximately 64 percent
of these services are sourced from firms
in the local market. The commenter
stated that costs of services purchased
from firms outside the hospital’s labor
market should be included with the
labor-related share of costs.
The commenter requested that CMS
provide evidence that pricing for
professional services provided by
regional and national firms to hospitals
is offered in a national market that is not
subject to geographic cost variation. The
commenter urged that, unless the
agency can produce strong evidence that
prices for professional services provided
by firms outside of a hospital’s local
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labor market are homogenous, CMS
restore the 1.2 percentage points it
proposed to reclassify to Professional
Services: Nonlabor-Related to the
Professional Services: Labor-Related
category.
Response: We respectfully disagree
with the commenter and continue to
believe it is appropriate that a
proportion of Accounting & Auditing,
Legal, Engineering, and Management
Consulting services costs purchased by
hospitals should be excluded from the
labor-related share.
As discussed in the RY 2007 IPF PPS
final rule (71 FR 27061), RY 2009 IPF
PPS (73 FR 25719) and the RY 2010 IPF
PPS notices (74 FR 20373), to provide
an adjustment for geographic wage
levels, the labor-related portion of an
IPF’s payment is adjusted using an
appropriate wage index. The purpose of
the labor-related share is to reflect the
proportion of the national PPS base
payment rate that is adjusted by the
hospital’s wage index (representing the
relative costs of their local labor market
to the national average). Therefore, we
include a cost category in the laborrelated share if the costs are laborintensive and vary with the local labor
market.
As acknowledged by the commenter
and confirmed by the survey of
hospitals conducted by CMS in 2008 (as
stated above), professional services can
be purchased from local firms as well as
national and regional professional
services firms. It is not necessarily the
case, as asserted by the commenter, that
these national and regional firms have
fees that match those in the local labor
market even though providers have the
option to utilize those firms. That is,
fees for services purchased from firms
outside the local labor market may differ
from those that would be purchased in
the local labor market for any number of
reasons (including but not limited to,
the skill level of the contracted
personnel, higher capital costs, etc.). As
noted earlier in this section of this final
rule, the definition for the labor-related
share requires the services to be
purchased in the local labor market;
therefore, CMS’s allocation of
approximately 64 percent of the
Professional Fees cost weight allocated
to the Professional Fees: Labor-Related
cost weight based on the 2008 survey
results 2 is consistent with the
commenter’s assertion that not all
Professional Fees services are purchased
2 The 64 percent value is based on a survey
conducted by CMS in 2008 as detailed in the FY
2010 IPPS/LTCH PPS final rule (74 FR 43850
through 43856). This was also used to determine
the Professional Fees: Labor-Related cost weight in
the 2016-based IPF market basket.
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in the local labor market. We believe it
is reasonable to conclude that costs of
those professional services purchased
directly within the local labor market
are directly related to local labor market
conditions (which are reflected in the
IPF’s respective wage index) and, thus,
should be included in the labor-related
share. The remaining approximately 36
percent of Professional Fees costs which
are purchased outside the local labor
market reflects different and additional
factors outside the local labor market
and, thus, should be excluded from the
labor-related share. In addition, we note
the compensation costs of professional
services provided by hospital employees
(which would reflect the local labor
market) are included in the labor-related
share, as they are included in the Wages
and Salaries and Benefit cost weights.
Therefore, for the reasons discussed,
we believe our proposed methodology
of allocating only a portion of
Professional Fees to the Professional
Fees: Labor-Related cost category is
appropriate. As stated previously,
effective for transmittal 18 (https://
www.cms.gov/Regulations-andGuidance/Guidance/Transmittals/
Transmittals/r18p240i), the hospital
Medicare Cost Report (CMS Form 2552–
10, OMB No. 0938–0050) is collecting
information on whether a hospital
purchased professional services (for
example, legal, accounting, tax
preparation, bookkeeping, payroll,
advertising, and/or management/
consulting services) from an unrelated
organization and if the majority of these
expenses were purchased from
unrelated organizations located outside
of the main hospital’s local area labor
market. We encourage all providers to
provide this information for potential
use in future rulemaking to determine
the labor-related share.
Comment: One commenter did not
support the proposed increase to the
labor-related share. This commenter
stated that any increase to the laborrelated share percentage penalizes any
facility that has a wage index less than
1.0. The commenter further stated that
across the country, there is a growing
disparity between high-wage and lowwage states that harms hospitals in
many rural and underserved
communities. The commenter stated
that limiting the increase in the laborrelated share would help mitigate that
growing disparity and recommended
that CMS consider excluding the labor
portion of capital-related costs for FY
2024 and going forward.
Response: As discussed in section
IV.D.1.a, the IPF PPS wage index is
applied to the labor-related portion of
an IPF’s payment to provide an
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adjustment for geographic wage levels.
The methodology to use the relative
importance values for the labor-related
cost categories from the most recent IPF
market basket is consistent with the
determination of the labor-related share
since the implementation of the IPF PPS
in 2007. The labor-related cost
categories reflect IPF costs that are
related to, influenced by, or vary with
the local labor market, which would
include a portion of the capital-related
costs since the construction costs for
capital infrastructure would be
influenced by the local labor market.
Therefore, we disagree with the
commenter that we should exclude the
labor portion of capital-related costs for
FY 2024 and going forward.
Comment: One commenter disagreed
with the assumption that home office
compensation costs that occur outside
of a hospital’s labor market are not
subject to geographic wage variation and
stated that they do not believe that the
proposed reclassification to the
Professional Fees: Non-Labor-Related
cost category is justified. The
commenters stated that the proposed
methodology fails to consider that the
home office is essentially a part of the
hospital, and thus the hospital, along
with its home office, is operating in
multiple labor markets. The commenters
stated that the home office’s portion of
the hospital’s labor costs should not be
excluded from the labor-related share
simply because they are not in the same
labor market as the hospital.
The commenter conducted their own
analysis of the Medicare cost report data
showing that providers with a home
office outside of their local labor market
had wage indexes both below 1 as well
as greater than 1. The commenter stated
that those hospitals in a labor market
with a wage index greater than 1 had
mean home office average hourly wage
costs that were greater than the mean
home office average hourly wage costs
of those hospitals in a labor market with
a wage index less than 1. The
commenter claimed that these data
indicate that, contrary to CMS’
assertion, home office salary, wage, and
benefit costs for hospitals with home
offices outside of their labor market are
subject to geographic wage variation.
The commenter requested that CMS
allocate the full 4.7 percentage points of
the Home Office/Related Organization
cost weight to the labor-related share.
Response: As discussed in the RY
2007 IPF PPS final rule (71 FR 27061),
RY 2009 IPF PPS (73 FR 25719) and the
RY 2010 IPF PPS notices (74 FR 20373),
to provide an adjustment for geographic
wage levels, the labor-related portion of
an IPF’s payment is adjusted using an
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appropriate wage index. Due to the
variation in costs and because of the
differences in geographic wage levels, in
the November 15, 2004 IPF PPS final
rule, we required that payment rates
under the IPF PPS be adjusted by a
geographic wage index. We proposed
and finalized a policy to use the
unadjusted, pre-floor, pre-reclassified
IPPS hospital wage index (representing
the wage level in the geographic area of
the hospital compared to the national
average hospital wage level as specified
under Section 1886(d)(3)(E)) to account
for geographic differences in IPF labor
costs. Therefore, consistent with the
definition of labor-related share used for
IPPS hospitals, we have included a cost
category in the labor-related share for
IPFs if the costs are labor-intensive and
vary with the local labor market (that is,
the geographic area of the hospital).
As the commenter stated, and as
validated with the Medicare cost report
data, a hospital’s home office can be
located outside the hospital’s local labor
market. For other types of professional
services, we only include the costs for
services purchased directly within the
geographic area of the hospital in the
labor-related share because they reflect
the local labor market conditions that
are consistent with the intent of the
geographic adjustment. We believe it is
reasonable to conclude that costs of
those home office services purchased
directly within the geographic area of
the hospital should also be included in
the labor-related share because they are
impacted by local labor market
conditions. As we have previously
discussed in the RY 2007 final rule (71
FR 27066), we believe that the actual
location of an IPF (as opposed to the
location of affiliated providers) is most
appropriate for determining the wage
adjustment, because the prevailing
wages in the area in which the IPF is
located influence the cost of a case. And
as we do for professional services, we
believe home office costs that are not in
the same geographic area as the hospital
should be excluded from the laborrelated share because they are
influenced by factors outside of the
hospital’s local labor market. To
implement this approach, we proposed
a methodology that relies on the
Medicare cost report data for hospitals
reporting home office information to
determine whether their home office is
in the same geographic area of the
hospital (which we define as the
hospital’s Metropolitan Statistical Area).
Our methodology determined that 46
percent of the Home Office/Related
Organization cost weight (reflecting
compensation costs) are associated with
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the geographic area of the hospital,
whereas the remaining 54 percent of
home office costs are purchased outside
the geographic area of the hospital.
Therefore, we believe our proposed
methodology of only allocating the
portion of the Home Office/Related
Organization cost weight (46 percent)
into the Professional Fees: LaborRelated cost weight that are purchased
in the same geographic area as the
hospital is appropriate as it is consistent
with the intent of the geographic
adjustment. In addition, we note that
the compensation costs for hospital
employees, which would reflect the
local labor market performing the same
tasks as home office personnel are
included in the labor-related share as
they are included in the Wages and
Salaries and Employee Benefits cost
weights.
As stated, we proposed to include in
the labor-related share the sum of the
relative importance of Wages and
Salaries, Employee Benefits,
Professional Fees: Labor-Related,
Administrative and Facilities Support
Services, Installation, Maintenance, and
Repair Services, All Other: LaborRelated Services, and a portion of the
Capital-Related cost weight from the
2021-based IPF market basket, as this
meets our definition of the labor-related
share with costs that are labor intensive
and vary with the local labor market.
Final Decision: After consideration of
public comments, we are finalizing the
2021-based IPF market basket proposed
labor-related cost categories and base
year cost weights as proposed.
We also proposed that if more recent
data were subsequently available, we
would use such data to determine the
FY 2024 labor-related share in the final
rule. Based on IGI’s second quarter 2023
forecast for the 2021-based IPF market
basket, the sum of the FY 2024 relative
importance for Wages and Salaries,
Employee Benefits, Professional Fees:
Labor-Related, Administrative and
Facilities Support Services, Installation
Maintenance & Repair Services, and All
Other: Labor-Related Services is 75.6
percent. The portion of Capital-Related
costs that is influenced by the local
labor market is estimated to be 46
percent, which is the same percentage
applied to the 2016-based IPF market
basket (84 FR 38446 through 38447).
Since the relative importance for
Capital-Related costs is 6.8 percent of
the 2021-based IPF market basket in FY
2024, we took 46 percent of 6.8 percent
to determine the labor-related share of
Capital-Related costs for FY 2024 of 3.1
percent. Therefore, the total laborrelated share for FY 2024 based on more
recent data is 78.7 percent (the sum of
75.6 percent for the operating costs and
3.1 percent for the labor-related share of
Capital-Related costs). Table 15 shows
the FY 2024 labor-related share using
the 2021-based IPF market basket
relative importance and the FY 2023
labor-related share using the 2016-based
IPF market basket.
The FY 2024 labor-related share using
the 2021-based IPF market basket is
about 1.0 percentage point higher than
the FY 2023 labor-related share using
the 2016-based IPF market basket. This
higher labor-related share is primarily
due to the incorporation of the 2021
Medicare cost report data, which
increased the Compensation cost weight
by 0.9 percentage point compared to the
2016-based IPF market basket, as shown
in Table 1 and Table 2 in section
IV.A.3.a.(2) of this final rule.
as the standard payment per day under
the IPF PPS and is adjusted by the
patient-level and facility-level
adjustments that are applicable to the
IPF stay. A detailed explanation of how
we calculated the average per diem cost
appears in the November 2004 IPF PPS
final rule (69 FR 66926).
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B. Updates to the IPF PPS Rates for FY
Beginning October 1, 2023
The IPF PPS is based on a
standardized Federal per diem base rate
calculated from the IPF average per
diem costs and adjusted for budget
neutrality in the implementation year.
The Federal per diem base rate is used
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1. Determining the Standardized
Budget-Neutral Federal Per Diem Base
Rate
Section 124(a)(1) of the BBRA
required that we implement the IPF PPS
in a budget-neutral manner. In other
words, the amount of total payments
under the IPF PPS, including any
payment adjustments, must be projected
to be equal to the amount of total
payments that would have been made if
the IPF PPS were not implemented.
Therefore, we calculated the budget
neutrality factor by setting the total
estimated IPF PPS payments to be equal
to the total estimated payments that
would have been made under the Tax
Equity and Fiscal Responsibility Act of
1982 (TEFRA) (Pub. L. 97–248)
methodology had the IPF PPS not been
implemented. A step-by-step
description of the methodology used to
estimate payments under the Tax Equity
and Fiscal Responsibility Act (TEFRA)
payment system appears in the
November 2004 IPF PPS final rule (69
FR 66926).
Under the IPF PPS methodology, we
calculated the final Federal per diem
base rate to be budget-neutral during the
IPF PPS implementation period (that is,
the 18-month period from January 1,
2005, through June 30, 2006) using a
July 1 update cycle. We updated the
average cost per day to the midpoint of
the IPF PPS implementation period
(October 1, 2005), and this amount was
used in the payment model to establish
the budget-neutrality adjustment.
Next, we standardized the IPF PPS
Federal per diem base rate to account
for the overall positive effects of the IPF
PPS payment adjustment factors by
dividing total estimated payments under
the TEFRA payment system by
estimated payments under the IPF PPS.
The information concerning this
standardization can be found in the
November 2004 IPF PPS final rule (69
FR 66932) and the RY 2006 IPF PPS
final rule (71 FR 27045). We then
reduced the standardized Federal per
diem base rate to account for the outlier
policy, the stop loss provision, and
anticipated behavioral changes. A
complete discussion of how we
calculated each component of the
budget neutrality adjustment appears in
the November 2004 IPF PPS final rule
(69 FR 66932 through 66933) and in the
RY 2007 IPF PPS final rule (71 FR 27044
through 27046). The final standardized
budget-neutral Federal per diem base
rate established for cost reporting
periods beginning on or after January 1,
2005, was calculated to be $575.95.
The Federal per diem base rate has
been updated in accordance with
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applicable statutory requirements and
§ 412.428 through publication of annual
notices or proposed and final rules. A
detailed discussion on the standardized
budget-neutral Federal per diem base
rate and the ECT payment per treatment
appears in the FY 2014 IPF PPS update
notice (78 FR 46738 through 46740).
These documents are available on the
CMS website at https://www.cms.gov/
Medicare/Medicare-Fee-for-ServicePayment/InpatientPsychFacilPPS/
index.html.
IPFs must include a valid procedure
code for ECT services provided to IPF
beneficiaries in order to bill for ECT
services, as described in our Medicare
Claims Processing Manual, Chapter 3,
Section 190.7.3 (available at https://
www.cms.gov/Regulations-andGuidance/Guidance/Manuals/
Downloads/clm104c03.pdf.) There were
no changes to the ECT procedure codes
used on IPF claims as a result of the
final update to the ICD–10–PCS code set
for FY 2024. Addendum B to this final
rule shows the ECT procedure codes for
FY 2024 and is available on our website
at https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
InpatientPsychFacilPPS/tools.html.
2. Update of the Federal Per Diem Base
Rate and Electroconvulsive Therapy
Payment Per Treatment
The current (FY 2023) Federal per
diem base rate is $865.63, and the ECT
payment per treatment is $372.67. For
the final FY 2024 Federal per diem base
rate, we applied the payment rate
update of 3.3 percent—that is, the 2021based IPF market basket increase for FY
2024 of 3.5 percent less the productivity
adjustment of 0.2 percentage point—and
the wage index budget-neutrality factor
of 1.0016 (as discussed in section IV.D.1
of this final rule) to the FY 2023 Federal
per diem base rate of $865.63, yielding
a final Federal per diem base rate of
$895.63 for FY 2024. Similarly, we
applied the 3.3 percent payment rate
update and the 1.0016 wage index
budget-neutrality factor to the FY 2023
ECT payment per treatment of $372.67,
yielding a final ECT payment per
treatment of $385.58 for FY 2024.
Section 1886(s)(4)(A)(i) of the Act
requires that for RY 2014 and each
subsequent RY, in the case of an IPF
that fails to report required data under
the IPFQR Program with respect to such
RY, the Secretary will reduce any
annual update to a standard federal rate
for discharges during the RY by 2.0
percentage points. Therefore, we are
applying a 2.0 percentage points
reduction to the Federal per diem base
rate and the ECT payment per treatment
as follows:
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• For IPFs that fail requirements
under the IPFQR Program, we applied a
1.3 percent payment rate update—that
is, the IPF market basket increase for FY
2024 of 3.5 percent less the productivity
adjustment of 0.2 percentage point for
an update of 3.3 percent, and further
reduced by 2.0 percentage points in
accordance with section 1886(s)(4)(A)(i)
of the Act—and the wage index budgetneutrality factor of 1.0016 to the FY
2023 Federal per diem base rate of
$865.63, yielding a Federal per diem
base rate of $878.29 for FY 2024.
• For IPFs that fail to meet
requirements under the IPFQR Program,
we applied a 1.3 percent annual
payment rate update and a 1.0016 wage
index budget-neutrality factor to the FY
2023 ECT payment per treatment of
$372.67 yielding an ECT payment per
treatment of $378.12 for FY 2024.
Lastly, we proposed that if more recent
data became available, we would use
such data, if appropriate, to determine
the FY 2024 Federal per diem base rate
and ECT payment per treatment for the
final rule.
Finally, we note that in the April 10,
2023 IPF PPS proposed rule (88 FR
21259), there were two technical errors
in describing the calculation of the FY
2024 proposed base rate and
electroconvulsive therapy (ECT)
payment per treatment for IPFs that fail
to meet requirements under the
Inpatient Psychiatric Facility Quality
Reporting (IPFQR) Program. In
describing the calculation of the FY
2024 Federal per diem base rate for IPFs
that fail to meet requirements under the
IPFQR Program, we inadvertently stated
that we applied the market basket
update, reduced by 2.0 percentage
points to the FY 2024 Federal per diem
base rate and FY 2024 ECT payment per
treatment. In accordance with our
longstanding methodology, and with the
actual calculation of these proposed
payment updates, the description of
these calculations should have used the
FY 2023 Federal per diem rate and FY
2023 ECT payment per treatment rather
than the FY 2024 Federal per diem rate
and ECT payment per treatment. To be
clear, these errors only affected the
description of the starting values from
which the rates were calculated, and the
calculations themselves, as well as the
rates indicated in the proposed rule,
were correct and consistent with our
longstanding methodology for updating
the IPF Federal per diem base rate and
ECT payment per treatment.
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C. Updates to the IPF PPS Patient-Level
Adjustment Factors
1. Overview of the IPF PPS Adjustment
Factors
The IPF PPS payment adjustments
were derived from a regression analysis
of 100 percent of the FY 2002 Medicare
Provider and Analysis Review
(MedPAR) data file, which contained
483,038 cases. For a more detailed
description of the data file used for the
regression analysis, see the November
2004 IPF PPS final rule (69 FR 66935
through 66936). We proposed to use the
existing regression-derived adjustment
factors established in 2005 for FY 2024.
However, we have used more recent
claims data to simulate payments to
finalize the outlier fixed dollar loss
threshold amount and to assess the
impact of the IPF PPS updates.
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2. IPF PPS Patient-Level Adjustments
The IPF PPS includes payment
adjustments for the following patientlevel characteristics: Medicare Severity
Diagnosis Related Groups (MS–DRGs)
assignment of the patient’s principal
diagnosis, selected comorbidities,
patient age, and the variable per diem
adjustments.
a. Update to MS–DRG Assignment
We believe it is important to maintain
for IPFs the same diagnostic coding and
Diagnosis Related Group (DRG)
classification used under the IPPS for
providing psychiatric care. For this
reason, when the IPF PPS was
implemented for cost reporting periods
beginning on or after January 1, 2005,
we adopted the same diagnostic code set
(ICD–9–CM) and DRG patient
classification system (MS–DRGs) that
were utilized at the time under the IPPS.
In the RY 2009 IPF PPS notice (73 FR
25709), we discussed CMS’s effort to
better recognize resource use and the
severity of illness among patients. CMS
adopted the new MS–DRGs for the IPPS
in the FY 2008 IPPS final rule with
comment period (72 FR 47130). In the
RY 2009 IPF PPS notice (73 FR 25716),
we provided a crosswalk to reflect
changes that were made under the IPF
PPS to adopt the new MS–DRGs. For a
detailed description of the mapping
changes from the original DRG
adjustment categories to the current
MS–DRG adjustment categories, we
refer readers to the RY 2009 IPF PPS
notice (73 FR 25714).
The IPF PPS includes payment
adjustments for designated psychiatric
DRGs assigned to the claim based on the
patient’s principal diagnosis. The DRG
adjustment factors were expressed
relative to the most frequently reported
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psychiatric DRG in FY 2002, that is,
DRG 430 (psychoses). The coefficient
values and adjustment factors were
derived from the regression analysis
discussed in detail in the November 28,
2003 IPF PPS proposed rule (68 FR
66923; 66928 through 66933) and the
November 15, 2004 IPF PPS final rule
(69 FR 66933 through 66960). Mapping
the DRGs to the MS–DRGs resulted in
the current 17 IPF MS–DRGs, instead of
the original 15 DRGs, for which the IPF
PPS provides an adjustment. For FY
2024, we did not propose any changes
to the IPF MS–DRG adjustment factors.
Therefore, we are retaining the existing
IPF MS–DRG adjustment factors.
In the FY 2015 IPF PPS final rule
published August 6, 2014, in the
Federal Register titled, ‘‘Inpatient
Psychiatric Facilities Prospective
Payment System—Update for FY
Beginning October 1, 2014 (FY 2015)’’
(79 FR 45945 through 45947), we
finalized conversions of the ICD–9–CMbased MS–DRGs to ICD–10–CM/PCSbased MS–DRGs, which were
implemented on October 1, 2015. As
discussed in the FY 2015 IPF PPS
proposed rule (79 FR 26047) in more
detail, every year, changes to the ICD–
10–CM and the ICD–10–PCS coding
system are addressed in the IPPS
proposed and final rules. The changes to
the codes are effective October 1 of each
year and must be used by acute care
hospitals as well as other providers to
report diagnostic and procedure
information. In accordance with
§ 412.428(e), the IPF PPS has always
incorporated ICD–10–CM and ICD–10–
PCS coding changes made in the annual
IPPS update and will continue to do so.
We will continue to publish coding
changes in a Transmittal/Change
Request, similar to how coding changes
are announced by the IPPS and LTCH
PPS. The coding changes relevant to the
IPF PPS are also published in the IPF
PPS proposed and final rules, or in IPF
PPS update notices. Further information
on the ICD–10–CM/PCS MS–DRG
conversion project can be found on the
CMS ICD–10–CM website at https://
www.cms.gov/Medicare/Coding/ICD10/
ICD-10-MS-DRG-ConversionProject.html.
For FY 2024, we proposed to continue
making the existing payment adjustment
for psychiatric diagnoses that group to
one of the existing 17 IPF MS–DRGs
listed in Addendum A. Addendum A is
available on our website at https://
www.cms.gov/Medicare/Medicare-Feefor-Service-Payment/
InpatientPsychFacilPPS/tools.html..
Psychiatric principal diagnoses that do
not group to one of the 17 designated
MS–DRGs will still receive the Federal
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per diem base rate and all other
applicable adjustments, but the payment
will not include an MS–DRG
adjustment.
As we did not propose any changes to
the IPF MS–DRG adjustment factors, we
are retaining the existing IPF MS–DRG
adjustment factors for FY 2024.
The diagnoses for each IPF MS–DRG
will be updated as of October 1, 2023,
using the final FY 2024 IPPS ICD–10–
CM/PCS code sets. The FY 2024 IPPS/
LTCH PPS final rule will include tables
of the changes to the ICD–10–CM/PCS
code sets, which underlie the FY 2024
IPF MS–DRGs. Both the FY 2024 IPPS
final rule and the tables of final changes
to the ICD–10–CM/PCS code sets, which
underlie the FY 2024 MS–DRGs, will be
available on the CMS IPPS website at
https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
AcuteInpatientPPS/.
Code First
As discussed in the ICD–10–CM
Official Guidelines for Coding and
Reporting, certain conditions have both
an underlying etiology and multiple
body system manifestations due to the
underlying etiology. For such
conditions, the ICD–10–CM has a
coding convention that requires the
underlying condition be sequenced first
followed by the manifestation.
Wherever such a combination exists,
there is a ‘‘use additional code’’ note at
the etiology code, and a ‘‘code first’’
note at the manifestation code. These
instructional notes indicate the proper
sequencing order of the codes (etiology
followed by manifestation). In
accordance with the ICD–10–CM
Official Guidelines for Coding and
Reporting, when a primary (psychiatric)
diagnosis code has a ‘‘code first’’ note,
the provider will follow the instructions
in the ICD–10–CM Tabular List. The
submitted claim goes through the CMS
processing system, which will identify
the principal diagnosis code as nonpsychiatric and search the secondary
codes for a psychiatric code to assign a
DRG code for adjustment. The system
will continue to search the secondary
codes for those that are appropriate for
comorbidity adjustment.
For more information on the code first
policy, we refer our readers to the
November 2004 IPF PPS final rule (69
FR 66945), and see sections I.A.13 and
I.B.7 of the FY 2020 ICD–10–CM Coding
Guidelines, available at https://
www.cdc.gov/nchs/data/icd/
10cmguidelines-FY2020_final.pdf. In
the FY 2015 IPF PPS final rule, we
provided a code first table for reference
that highlights the same or similar
manifestation codes where the code first
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instructions apply in ICD–10–CM that
were present in ICD–10–CM (79 FR
46009). In FY 2018, FY 2019 and FY
2020, there were no changes to the final
ICD–10–CM codes in the IPF Code First
table. For FY 2021 and FY 2022, there
were 18 ICD–10–CM codes deleted from
the final IPF Code First table. For FY
2023, there were 2 ICD–10–CM codes
deleted and 48 ICD–10–CM codes added
to the IPF Code First table.
For FY 2024, there were no proposed
changes to the Code First Table. For this
final rule, we are finalizing the deletion
of 1 ICD–10–CM code and the addition
of 5 ICD–10–CM codes as ‘‘code first’’
codes. There are 26 codes whose ‘‘code
first’’ codes are being updated in the IPF
Code First Table to reflect these changes
In accordance with our longstanding
practice for the IPF PPS and with
§ 412.428(e), we are adopting these
latest ICD–10–CM changes for October,
2023 and describing these changes in
this FY 2024 IPF PPS final rule. The FY
2024 Code First table is shown in
Addendum B on the CMS website at
https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
InpatientPsychFacilPPS/tools.html.
b. Payment for Comorbid Conditions
The intent of the comorbidity
adjustments is to recognize the
increased costs associated with
comorbid conditions by providing
additional payments for certain existing
medical or psychiatric conditions that
are expensive to treat. In our RY 2012
IPF PPS final rule (76 FR 26451 through
26452), we explained that the IPF PPS
includes 17 comorbidity categories and
identified the new, revised, and deleted
ICD–9–CM diagnosis codes that generate
a comorbid condition payment
adjustment under the IPF PPS for RY
2012 (76 FR 26451).
Comorbidities are specific patient
conditions that are secondary to the
patient’s principal diagnosis and that
require treatment during the stay.
Diagnoses that relate to an earlier
episode of care and have no bearing on
the current hospital stay are excluded
and must not be reported on IPF claims.
Comorbid conditions must exist at the
time of admission or develop
subsequently, and affect the treatment
received, LOS, or both treatment and
LOS.
For each claim, an IPF may receive
only one comorbidity adjustment within
a comorbidity category, but it may
receive an adjustment for more than one
comorbidity category. Current billing
instructions for discharge claims, on or
after October 1, 2015, require IPFs to
enter the complete ICD–10–CM codes
for up to 24 additional diagnoses if they
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co-exist at the time of admission, or
develop subsequently and impact the
treatment provided.
The comorbidity adjustments were
determined based on the regression
analysis using the diagnoses reported by
IPFs in FY 2002. The principal
diagnoses were used to establish the
DRG adjustments and were not
accounted for in establishing the
comorbidity category adjustments,
except where ICD–9–CM code first
instructions applied. In a code first
situation, the submitted claim goes
through the CMS processing system,
which will identify the principal
diagnosis code as non-psychiatric and
search the secondary codes for a
psychiatric code to assign an MS–DRG
code for adjustment. The system will
continue to search the secondary codes
for those that are appropriate for
comorbidity adjustment.
As noted previously, it is our policy
to maintain the same diagnostic coding
set for IPFs that is used under the IPPS
for providing the same psychiatric care.
The 17 comorbidity categories formerly
defined using ICD–9–CM codes were
converted to ICD–10–CM/PCS in our FY
2015 IPF PPS final rule (79 FR 45947
through 45955). The goal for converting
the comorbidity categories is referred to
as replication, meaning that the
payment adjustment for a given patient
encounter is the same after ICD–10–CM
implementation as it would be if the
same record had been coded in ICD–9–
CM and submitted prior to ICD–10–CM/
PCS implementation on October 1,
2015. All conversion efforts were made
with the intent of achieving this goal.
For FY 2024, we proposed to use the
same comorbidity adjustment factors in
effect in FY 2023. The FY 2024
comorbidity adjustment factors are
found in Addendum A, available on the
CMS website at https://www.cms.gov/
Medicare/Medicare-Fee-for-ServicePayment/InpatientPsychFacilPPS/
tools.html.
For FY 2024, we proposed to add 2
ICD–10–CM codes and remove 1 ICD–
10–CM code from the Chronic Renal
Failure category. We did not receive any
comments on this proposal, and we are
finalizing these changes as proposed. In
addition, we are adding 2 ICD–10–CM
codes to the Chronic Obstructive
Pulmonary Disease category, 1 ICD–10–
CM code to the Infectious Disease
category, 4 ICD–10–CM codes to the
Poisoning category, 6 ICD–10–PCS
codes for the Oncology Treatment
Procedure category. For the Oncology
Treatment Diagnosis Category, we are
adding 12 ICD–10–CM codes and
deleting 2 ICD–10–CM codes. Finally,
for the Acute Renal Failure Category, we
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are adding 1 ICD–10–CM code and
deleting 1 ICD–10_CM code. In
accordance with our longstanding
practice for the IPF PPS and with
§ 412.428(e), we are adopting these
latest ICD–10–CM changes for October,
2023 and describing these changes in
this FY 2024 IPF PPS final rule.
The FY 2024 comorbidity codes are
shown in Addenda B, available on the
CMS website at https://www.cms.gov/
Medicare/Medicare-Fee-for-ServicePayment/InpatientPsychFacilPPS/
tools.html.
In accordance with the policy
established in the FY 2015 IPF PPS final
rule (79 FR 45949 through 45952), we
reviewed all new FY 2024 ICD–10–CM
codes to remove codes that were site
‘‘unspecified’’ in terms of laterality from
the FY 2024 ICD–10–CM/PCS codes in
instances where more specific codes are
available. As we stated in the FY 2015
IPF PPS final rule, we believe that
specific diagnosis codes that narrowly
identify anatomical sites where disease,
injury, or a condition exists should be
used when coding patients’ diagnoses
whenever these codes are available. We
finalized in the FY 2015 IPF PPS rule,
that we will remove site ‘‘unspecified’’
codes from the IPF PPS ICD–10–CM/
PCS codes in instances when laterality
codes (site specified codes) are
available, as the clinician should be able
to identify a more specific diagnosis
based on clinical assessment at the
medical encounter. None of the
finalized additions to the FY 2024 ICD–
10–CM/PCS codes were site
‘‘unspecified’’ by laterality; therefore,
we are not removing any of the new
codes.
c. Patient Age Adjustments
As explained in the November 2004
IPF PPS final rule (69 FR 66922), we
analyzed the impact of age on per diem
cost by examining the age variable
(range of ages) for payment adjustments.
In general, we found that the cost per
day increases with age. The older age
groups are costlier than the under 45 age
group, the differences in per diem cost
increase for each successive age group,
and the differences are statistically
significant. For FY 2024, we proposed
continuing to use the patient age
adjustments currently in effect for FY
2023, as shown in Addendum A of this
final rule (see https://www.cms.gov/
Medicare/Medicare-Fee-for-ServicePayment/InpatientPsychFacilPPS/
tools.html).
As we did not propose any changes to
the patient age adjustment factors, we
are retaining the existing patient age
adjustment factors for FY 2024.
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d. Variable Per Diem Adjustments
We explained in the November 2004
IPF PPS final rule (69 FR 66946) that the
regression analysis indicated that per
diem cost declines as the LOS increases.
The variable per diem adjustments to
the Federal per diem base rate account
for ancillary and administrative costs
that occur disproportionately in the first
days after admission to an IPF. As
discussed in the November 2004 IPF
PPS final rule, we used a regression
analysis to estimate the average
differences in per diem cost among stays
of different lengths (69 FR 66947
through 66950). As a result of this
analysis, we established variable per
diem adjustments that begin on day 1
and decline gradually until day 21 of a
patient’s stay. For day 22 and thereafter,
the variable per diem adjustment
remains the same each day for the
remainder of the stay. However, the
adjustment applied to day 1 depends
upon whether the IPF has a qualifying
ED. If an IPF has a qualifying ED, it
receives a 1.31 adjustment factor for day
1 of each stay. If an IPF does not have
a qualifying ED, it receives a 1.19
adjustment factor for day 1 of the stay.
The ED adjustment is explained in more
detail in section IV.D.4 of this final rule.
For FY 2024, we proposed to use the
variable per diem adjustment factors
currently in effect in FY 2023, as shown
in Addendum A to this final rule
(available at https://www.cms.gov/
Medicare/Medicare-Fee-for-ServicePayment/InpatientPsychFacilPPS/
tools.html). A complete discussion of
the variable per diem adjustments
appears in the November 2004 IPF PPS
final rule (69 FR 66946).
As we did not propose any changes to
the variable per diem adjustment
factors, we are retaining the existing
variable per diem adjustment factors for
FY 2024.
D. Updates to the IPF PPS Facility-Level
Adjustments
The IPF PPS includes facility-level
adjustments for the wage index, IPFs
located in rural areas, teaching IPFs,
cost of living adjustments for IPFs
located in Alaska and Hawaii, and IPFs
with a qualifying ED.
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1. Wage Index Adjustment
a. Background
As discussed in the RY 2007 IPF PPS
final rule (71 FR 27061), RY 2009 IPF
PPS (73 FR 25719) and the RY 2010 IPF
PPS notices (74 FR 20373), to provide
an adjustment for geographic wage
levels, the labor-related portion of an
IPF’s payment is adjusted using an
appropriate wage index. Currently, an
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IPF’s geographic wage index value is
determined based on the actual location
of the IPF in an urban or rural area, as
defined in 42 CFR 412.64(b)(1)(ii)(A)
and (C).
Due to the variation in costs and
because of the differences in geographic
wage levels, in the November 15, 2004
IPF PPS final rule, we required that
payment rates under the IPF PPS be
adjusted by a geographic wage index.
We proposed and finalized a policy to
use the unadjusted, pre-floor, prereclassified IPPS hospital wage index to
account for geographic differences in
IPF labor costs. We implemented use of
the pre-floor, pre-reclassified IPPS
hospital wage data to compute the IPF
wage index since there was not an IPFspecific wage index available. We
believe that IPFs generally compete in
the same labor market as IPPS hospitals,
so the pre-floor, pre-reclassified IPPS
hospital wage data should be reflective
of labor costs of IPFs. We believe this
pre-floor, pre-reclassified IPPS hospital
wage index to be the best available data
to use as proxy for an IPF specific wage
index. As discussed in the RY 2007 IPF
PPS final rule (71 FR 27061 through
27067), under the IPF PPS, the wage
index is calculated using the IPPS wage
index for the labor market area in which
the IPF is located, without considering
geographic reclassifications, floors, and
other adjustments made to the wage
index under the IPPS. For a complete
description of these IPPS wage index
adjustments, we refer readers to the FY
2019 IPPS/LTCH PPS final rule (83 FR
41362 through 41390). Our wage index
policy at § 412.424(a)(2), requires that
we use the best Medicare data available
to estimate costs per day, including an
appropriate wage index to adjust for
wage differences.
When the IPF PPS was implemented
in the November 15, 2004 IPF PPS final
rule, with an effective date of January 1,
2005, the pre-floor, pre-reclassified IPPS
hospital wage index that was available
at the time was the FY 2005 pre-floor,
pre-reclassified IPPS hospital wage
index. Historically, the IPF wage index
for a given RY has used the pre-floor,
pre-reclassified IPPS hospital wage
index from the prior FY as its basis.
This has been due in part to the prefloor, pre-reclassified IPPS hospital
wage index data that were available
during the IPF rulemaking cycle, where
an annual IPF notice or IPF PPS final
rule was usually published in early
May. This publication timeframe was
relatively early compared to other
Medicare payment rules, because the
IPF PPS follows a RY, which was
defined in the implementation of the
IPF PPS as the 12-month period from
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July 1 to June 30 (69 FR 66927).
Therefore, the best available data at the
time the IPF PPS was implemented was
the pre-floor, pre-reclassified IPPS
hospital wage index from the prior FY
(for example, the RY 2006 IPF wage
index was based on the FY 2005 prefloor, pre-reclassified IPPS hospital
wage index).
In the RY 2012 IPF PPS final rule, we
changed the reporting year timeframe
for IPFs from a RY to the FY, which
begins October 1 and ends September 30
(76 FR 26434 through 26435). In that RY
2012 IPF PPS final rule, we continued
our established policy of using the prefloor, pre-reclassified IPPS hospital
wage index from the prior year (that is,
from FY 2011) as the basis for the FY
2012 IPF wage index. This policy of
basing a wage index on the prior year’s
pre-floor, pre-reclassified IPPS hospital
wage index has been followed by other
Medicare payment systems, such as
hospice and inpatient rehabilitation
facilities. By continuing with our
established policy, we remained
consistent with other Medicare payment
systems.
In FY 2020, we finalized the IPF wage
index methodology to align the IPF PPS
wage index with the same wage data
timeframe used by the IPPS for FY 2020
and subsequent years. Specifically, we
finalized to use the pre-floor, prereclassified IPPS hospital wage index
from the FY concurrent with the IPF FY
as the basis for the IPF wage index. For
example, the FY 2020 IPF wage index
was based on the FY 2020 pre-floor, prereclassified IPPS hospital wage index
rather than on the FY 2019 pre-floor,
pre-reclassified IPPS hospital wage
index.
We explained in the FY 2020
proposed rule (84 FR 16973), that using
the concurrent pre-floor, pre-reclassified
IPPS hospital wage index will result in
the most up-to-date wage data being the
basis for the IPF wage index. It will also
result in more consistency and parity in
the wage index methodology used by
other Medicare payment systems. The
Medicare SNF PPS already used the
concurrent IPPS hospital wage index
data as the basis for the SNF PPS wage
index. Thus, the wage adjusted
Medicare payments of various provider
types will be based upon wage index
data from the same timeframe. CMS
proposed similar policies to use the
concurrent pre-floor, pre-reclassified
IPPS hospital wage index data in other
Medicare payment systems, such as
hospice and inpatient rehabilitation
facilities. For FY 2024, we proposed to
continue using the concurrent pre-floor,
pre-reclassified IPPS hospital wage
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index as the basis for the IPF wage
index.
We proposed to apply the IPF wage
index adjustment to the labor-related
share of the national base rate and ECT
payment per treatment. The laborrelated share of the national rate and
ECT payment per treatment would
change from 77.4 percent in FY 2023 to
78.7 percent in FY 2024. This
percentage reflects the labor-related
share of the 2021-based IPF market
basket for FY 2024 (see section IV.A of
this final rule).
Comment: Several commenters urged
CMS to revise the IPF wage index
methodology. Specifically, a few
commenters suggested CMS revise the
policy so that the post-reclassification
and post-floor hospital IPPS wage index
is used to calculate the wage index for
IPFs. The commenter believes that the
continued use of the pre-reclassification
and pre-floor hospital inpatient wage
index is unreasonable because it places
IPFs at a disadvantage in the labor
markets in which they operate relative
to hospitals in the same markets.
Other commenters suggested CMS
exercise its authority to refine the IPF
PPS by applying the pre-floor, prereclassified IPPS hospital wage index
for the CBSA in which the nearest IPPS
hospital is located where the pre-floor,
pre-classified IPPS hospital wage index
for the CBSA in which the IPF is located
only includes data from a closed IPPS
hospital. Commenters stated they
believe the closed hospital data is more
likely to be unreliable such that the
application of the pre-floor, prereclassified IPPS hospital wage index
would result in an inappropriately
deflated wage index value. Commenters
further asserted that the closure of the
only IPPS hospital in the CBSA would
suggest that the community is currently
underserved, and would make it
particularly appropriate to ensure that
aberrant wage index data does not serve
as an impediment to new IPF services
in a community.
Response: We appreciate the
commenters’ recommendations. We did
not propose the specific policies
suggested by commenters, but we will
take them into consideration to
potentially inform future rulemaking.
We do not believe that the continued
use of the pre-reclassification and prefloor hospital inpatient wage index for
FY 2024 is unreasonable or that this
policy puts IPFs at a disadvantage
relative to hospitals in the labor markets
in which they operate. As we have
previously discussed in the RY 2007
final rule (71 FR 27066), we believe that
the actual location of an IPF (as opposed
to the location of affiliated providers) is
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most appropriate for determining the
wage adjustment, because the prevailing
wages in the area in which the IPF is
located influence the cost of a case. In
that same RY 2007 final rule (71 FR
27066), we also stated that we believe
the ‘‘rural floor’’ is required only for the
acute care hospital payment system,
because section 4410 of the Balanced
Budget Act of 1997 (Pub. L. 105–33)
applies specifically to acute care
hospitals and not excluded hospitals
and excluded units. As we have
previously discussed, the IPF wage
index is intended to be a relative
measure of the value of labor in
prescribed labor market areas (87 FR
46857). There is a variety of reasons
why our longstanding IPF wage index
policy has not applied floors or
reclassifications, which as we
previously noted, are not applied to the
IPF wage index by statute. For example,
applying floors and reclassifications to
the IPF wage index would significantly
increase administrative burden, both for
IPFs and for CMS, that would be
associated with IPFs reclassifying from
one CBSA to another, and it would
significantly increase the complexity of
the methodology. Furthermore, because
floors and reclassifications would be
applied budget-neutrally under the
wage index, these policies would
increase the wage index for some IPFs
while reducing IPF PPS payments for all
other IPFs, which would upset the longsettled expectations with which IPFs
across the country have been operating.
For these reasons, we believe using the
pre-floor, pre-reclassified IPPS hospital
wage index is the most appropriate data
to use as a proxy for an IPF wage index.
Regarding the suggestion to apply the
wage index for the CBSA of the nearest
IPPS hospital in cases when an IPF’s
CBSA includes only a closed IPPS
hospital, we disagree with the
commenter that wage data from a
hospital that has subsequently closed is
more likely to be unreliable and that
such data would inappropriately deflate
the wage index for that CBSA. Rather,
following the longstanding methodology
for calculating the wage index, wage
data from the period during which the
hospital was open would be comparable
to wage data from the same period for
hospitals located in other geographical
areas, and would provide an appropriate
relative measure of the value of labor in
that CBSA’s labor market area compared
to others. We do not believe that such
wage data or the wage index of a CBSA
in this situation would serve as an
impediment for either new or existing
IPF services in a community. In
addition, we recognize that in some
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cases, the closure of the only IPPS
hospital in the CBSA could suggest that
the community is underserved;
however, in other cases, the lack of an
IPPS hospital could be due to other
factors, such as when an area’s only
IPPS hospital converts to another
hospital type such as a CAH. We note
that at this time, there is only one urban
CBSA with no IPPS hospitals; however,
there are also no IPFs located in this
CBSA.
Lastly, as discussed in the FY 2024
IPPS proposed rule (88 FR 26966) in
constructing the proposed FY 2024
wage index, wage data was included for
facilities that were IPPS hospitals in FY
2020, inclusive of those facilities that
have since terminated their
participation in the program as
hospitals, as long as those data did not
fail any of our edits for reasonableness.
We believe that including the wage data
for these hospitals is, in general,
appropriate to reflect the economic
conditions in the various labor market
areas during the relevant past period
and to ensure that the current wage
index represents the labor market area’s
current wages as compared to the
national average of wages.
Final Decision: After consideration of
the comments received, we are
finalizing our proposal for FY 2024 to
continue to use the concurrent pre-floor,
pre-reclassified IPPS hospital wage
index as the basis for the IPF wage
index.
We will apply the IPF wage index
adjustment to the labor-related share of
the national base rate and ECT payment
per treatment. The labor-related share of
the national rate and ECT payment per
treatment will change from 77.4 percent
in FY 2023 to 78.7 percent in FY 2024.
This percentage reflects the laborrelated share of the 2021-based IPF
market basket for FY 2024 (see section
IV.A.5 of this final rule).
b. Office of Management and Budget
(OMB) Bulletins
i. Background
The wage index used for the IPF PPS
is calculated using the unadjusted, prereclassified and pre-floor IPPS wage
index data and is assigned to the IPF on
the basis of the labor market area in
which the IPF is geographically located.
IPF labor market areas are delineated
based on the CBSAs established by the
OMB.
Generally, OMB issues major
revisions to statistical areas every 10
years, based on the results of the
decennial census. However, OMB
occasionally issues minor updates and
revisions to statistical areas in the years
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between the decennial censuses through
OMB Bulletins. These bulletins contain
information regarding CBSA changes,
including changes to CBSA numbers
and titles. OMB bulletins may be
accessed online at https://
www.whitehouse.gov/wp-content/
uploads/2020/03/Bulletin-20-01.pdf. In
accordance with our established
methodology, the IPF PPS has
historically adopted any CBSA changes
that are published in the OMB bulletin
that corresponds with the IPPS hospital
wage index used to determine the IPF
wage index and, when necessary and
appropriate, has proposed and finalized
transition policies for these changes.
In the RY 2007 IPF PPS final rule (71
FR 27061 through 27067), we adopted
the changes discussed in the OMB
Bulletin No. 03–04 (June 6, 2003),
which announced revised definitions
for Micropolitan Statistical Areas and
the creation of Micropolitan Statistical
Areas and Combined Statistical Areas.
In adopting the OMB CBSA geographic
designations in RY 2007, we did not
provide a separate transition for the
CBSA-based wage index since the IPF
PPS was already in a transition period
from TEFRA payments to PPS
payments.
In the RY 2009 IPF PPS notice, we
incorporated the CBSA nomenclature
changes published in the most recent
OMB bulletin that applied to the IPPS
hospital wage index used to determine
the current IPF wage index and stated
that we expected to continue to do the
same for all the OMB CBSA
nomenclature changes in future IPF PPS
rules and notices, as necessary (73 FR
25721).
Subsequently, CMS adopted the
changes that were published in past
OMB bulletins in the FY 2016 IPF PPS
final rule (80 FR 46682 through 46689),
the FY 2018 IPF PPS rate update (82 FR
36778 through 36779), the FY 2020 IPF
PPS final rule (84 FR 38453 through
38454), and the FY 2021 IPF PPS final
rule (85 FR 47051 through 47059). We
direct readers to each of these rules for
more information about the changes that
were adopted and any associated
transition policies.
In part due to the scope of changes
involved in adopting the CBSA
delineations for FY 2021, we finalized a
2-year transition policy consistent with
our past practice of using transition
policies to help mitigate negative
impacts on hospitals of certain wage
index policy changes. We applied a 5percent cap on wage index decreases to
all IPF providers that had any decrease
in their wage indexes, regardless of the
circumstance causing the decline, so
that an IPF’s final wage index for FY
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2021 will not be less than 95 percent of
its final wage index for FY 2020,
regardless of whether the IPF was part
of an updated CBSA. We refer readers
to the FY 2021 IPF PPS final rule (85 FR
47058 through 47059) for a more
detailed discussion about the wage
index transition policy for FY 2021.
On March 6, 2020 OMB issued OMB
Bulletin 20–01 (available on the web at
https://www.whitehouse.gov/wpcontent/uploads/2020/03/Bulletin-2001.pdf). In considering whether to adopt
this bulletin, we analyzed whether the
changes in this bulletin would have a
material impact on the IPF PPS wage
index. This bulletin creates only one
Micropolitan statistical area. As
discussed in further detail in section
IV.D.1.b.ii of this final rule, since
Micropolitan areas are considered rural
for the IPF PPS wage index, this bulletin
has no material impact on the IPF PPS
wage index. That is, the constituent
county of the new Micropolitan area
was considered rural effective as of FY
2021 and would continue to be
considered rural if we adopted OMB
Bulletin 20–01. Therefore, we did not
propose to adopt OMB Bulletin 20–01 in
the FY 2022 IPF PPS proposed rule.
In the FY 2023 IPF PPS final rule (87
FR 46856 through 46859), we finalized
a permanent 5-percent cap on any
decrease to a provider’s wage index
from its wage index in the prior year,
and we stated that we would apply this
cap in a budget-neutral manner.
Additionally, we finalized a policy that
a new IPF would be paid the wage index
for the area in which it is geographically
located for its first full or partial FY
with no cap applied because a new IPF
would not have a wage index in the
prior FY. We amended the IPF PPS
regulations at § 412.424(d)(1)(i) to reflect
this permanent cap on wage index
decreases. We refer readers to the FY
2023 IPF PPS final rule for a more
detailed discussion about this policy.
ii. Micropolitan Statistical Areas (MSA)
OMB defines a ‘‘Micropolitan
Statistical Area’’ as a CBSA associated
with at least one urban cluster that has
a population of at least 10,000, but less
than 50,000 (75 FR 37252). We refer to
these as Micropolitan Areas. After
extensive impact analysis, consistent
with the treatment of these areas under
the IPPS as discussed in the FY 2005
IPPS final rule (69 FR 49029 through
49032), we determined the best course
of action would be to treat Micropolitan
Areas as ‘‘rural’’ and include them in
the calculation of each state’s IPF PPS
rural wage index. We refer the reader to
the FY 2007 IPF PPS final rule (71 FR
27064 through 27065) for a complete
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discussion regarding treating
Micropolitan Areas as rural.
c. Adjustment for Rural Location
In the November 2004 IPF PPS final
rule, (69 FR 66954), we provided a 17
percent payment adjustment for IPFs
located in a rural area. This adjustment
was based on the regression analysis,
which indicated that the per diem cost
of rural facilities was 17 percent higher
than that of urban facilities after
accounting for the influence of the other
variables included in the regression.
This 17 percent adjustment has been
part of the IPF PPS each year since the
inception of the IPF PPS. For FY 2024,
we proposed to apply a 17 percent
payment adjustment for IPFs located in
a rural area as defined at
§ 412.64(b)(1)(ii)(C) (see 69 FR 66954 for
a complete discussion of the adjustment
for rural locations).
d. Budget Neutrality Adjustment
Changes to the wage index are made
in a budget-neutral manner so that
updates do not increase expenditures.
Therefore, for FY 2024, we proposed to
apply a budget-neutrality adjustment in
accordance with our existing budgetneutrality policy. This policy requires
us to update the wage index in such a
way that total estimated payments to
IPFs for FY 2024 are the same with or
without the changes (that is, in a
budget-neutral manner) by applying a
budget-neutrality factor to the IPF PPS
rates. We use the following steps to
ensure that the rates reflect the FY 2024
update to the wage indexes (based on
the FY 2020 hospital cost report data)
and the labor-related share in a budgetneutral manner:
Step 1: Simulate estimated IPF PPS
payments, using the FY 2023 IPF wage
index values (available on the CMS
website) and labor-related share (as
published in the FY 2023 IPF PPS final
rule (87 FR 46846).
Step 2: Simulate estimated IPF PPS
payments using the FY 2024 IPF wage
index values (available on the CMS
website) and FY 2024 labor-related
share (based on the latest available data
as discussed previously).
Step 3: Divide the amount calculated
in step 1 by the amount calculated in
step 2. The resulting quotient is the FY
2024 budget-neutral wage adjustment
factor of 1.0016.
Step 4: Apply the FY 2024 budgetneutral wage adjustment factor from
step 3 to the FY 2023 IPF PPS Federal
per diem base rate after the application
of the market basket update described in
section IV.A of this final rule, to
determine the FY 2024 IPF PPS Federal
per diem base rate.
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2. Teaching Adjustment
a. Background
In the November 2004 IPF PPS final
rule, we implemented regulations at
§ 412.424(d)(1)(iii) to establish a facilitylevel adjustment for IPFs that are, or are
part of, teaching hospitals. The teaching
adjustment accounts for the higher
indirect operating costs experienced by
hospitals that participate in graduate
medical education (GME) programs. The
payment adjustments are made based on
the ratio of the number of fulltime
equivalent (FTE) interns and residents
training in the IPF and the IPF’s average
daily census.
Medicare makes direct GME payments
(for direct costs such as resident and
teaching physician salaries, and other
direct teaching costs) to all teaching
hospitals including those paid under a
PPS, and those paid under the TEFRA
rate-of-increase limits. These direct
GME payments are made separately
from payments for hospital operating
costs and are not part of the IPF PPS.
The direct GME payments do not
address the estimated higher indirect
operating costs teaching hospitals may
face.
The results of the regression analysis
of FY 2002 IPF data established the
basis for the payment adjustments
included in the November 2004 IPF PPS
final rule. The results showed that the
indirect teaching cost variable is
significant in explaining the higher
costs of IPFs that have teaching
programs. We calculated the teaching
adjustment based on the IPF’s ‘‘teaching
variable’’, which is (1 + [the number of
FTE residents training in the IPF’s
average daily census]). The teaching
variable is then raised to the 0.5150
power to result in the teaching
adjustment. This formula is subject to
the limitations on the number of FTE
residents, which are described in this
section of this final rule.
We established the teaching
adjustment in a manner that limited the
incentives for IPFs to add FTE residents
for the purpose of increasing their
teaching adjustment. We imposed a cap
on the number of FTE residents that
may be counted for purposes of
calculating the teaching adjustment. The
cap limits the number of FTE residents
that teaching IPFs may count for the
purpose of calculating the IPF PPS
teaching adjustment, not the number of
residents teaching institutions can hire
or train. We calculated the number of
FTE residents that trained in the IPF
during a ‘‘base year’’ and used that FTE
resident number as the cap. An IPF’s
FTE resident cap is ultimately
determined based on the final
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settlement of the IPF’s most recent cost
report filed before November 15, 2004
(69 FR 66955). A complete discussion of
the temporary adjustment to the FTE
cap to reflect residents due to hospital
closure or residency program closure
appears in the RY 2012 IPF PPS
proposed rule (76 FR 5018 through
5020) and the RY 2012 IPF PPS final
rule (76 FR 26453 through 26456).
In the regression analysis, the
logarithm of the teaching variable had a
coefficient value of 0.5150. We
converted this cost effect to a teaching
payment adjustment by treating the
regression coefficient as an exponent
and raising the teaching variable to a
power equal to the coefficient value. We
note that the coefficient value of 0.5150
was based on the regression analysis
holding all other components of the
payment system constant. A complete
discussion of how the teaching
adjustment was calculated appears in
the November 2004 IPF PPS final rule
(69 FR 66954 through 66957) and the
RY 2009 IPF PPS notice (73 FR 25721).
As with other adjustment factors
derived through the regression analysis,
we do not plan to propose updates to
the teaching adjustment factors until we
more fully analyze IPF PPS data.
Therefore, in this FY 2024 final rule, we
are retaining the coefficient value of
0.5150 for the teaching adjustment to
the Federal per diem base rate.
Comment: One commenter
recommended CMS update its
methodology for calculating the IPF
teaching adjustment, particularly in
recognition of the Congress authorizing
the awarding of new Medicarereimbursable residency positions under
the CAA, 2023 and the Consolidated
Appropriations Act, 2021 (hereafter
referred to as CAA, 2021) (Pub. L. 116–
260). This commenter suggested CMS
collect information on awards of new
Medicare residency positions under
section 126 of division CC, CAA, 2021
and section 4122 of CAA, 2023 from
those hospitals subject to the IPF so that
it can provide resident FTE cap
increases under the IPF for those
hospitals that receive awards for
psychiatry programs.
One commenter requested that CMS
permit IPFs to aggregate and adjust their
FTE caps through affiliation agreements.
The commenter noted training residents
often indirectly increases the hospital’s
operational costs, but freestanding IPFs
that take over this role are unable to
receive any corresponding payment
increase that was previously available to
the host-hospital distinct part unit
(DPU).
Response: We appreciate the
commenter’s suggestion regarding
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potential changes to the IPF teaching
adjustment to recognize new Medicarereimbursable residency positions under
the CAA, 2023 and the CAA, 2021. The
CAA, 2021 and CAA, 2023 established
resident slots for direct medical
education and indirect medical
education, which are paid under the
IPPS. We will take this comment into
consideration to potentially inform
future rulemaking for the IPF PPS.
Regarding the commenter’s suggestion
to recognize affiliation agreements, we
did not propose to recognize affiliation
agreements for the IPF PPS teaching
adjustment and are not making a change
to this policy. As we previously stated
in the RY 2005 IPF PPS final rule (69
FR 66956), our intent is not to affect
affiliation agreements and rotational
arrangements for hospitals that have
residents that train in more than one
hospital. We have not implemented a
provision concerning affiliation
agreements specifically pertaining to the
FTE caps used in the teaching
adjustment under the IPF PPS.
Final Decision: We are finalizing as
proposed to calculate the IPF teaching
adjustment according to our established
methodology.
3. Cost of Living Adjustment (COLA) for
IPFs Located in Alaska and Hawaii
The IPF PPS includes a payment
adjustment for IPFs located in Alaska
and Hawaii based upon the area in
which the IPF is located. As we
explained in the November 2004 IPF
PPS final rule, the FY 2002 data
demonstrated that IPFs in Alaska and
Hawaii had per diem costs that were
disproportionately higher than other
IPFs. Other Medicare prospective
payment systems (for example, the IPPS
and LTCH PPS) adopted a COLA to
account for the cost differential of care
furnished in Alaska and Hawaii.
We analyzed the effect of applying a
COLA to payments for IPFs located in
Alaska and Hawaii. The results of our
analysis demonstrated that a COLA for
IPFs located in Alaska and Hawaii will
improve payment equity for these
facilities. As a result of this analysis, we
provided a COLA in the November 2004
IPF PPS final rule.
A COLA for IPFs located in Alaska
and Hawaii is made by multiplying the
non-labor-related portion of the Federal
per diem base rate by the applicable
COLA factor based on the COLA area in
which the IPF is located.
The COLA factors through 2009 were
published by the Office of Personnel
Management (OPM), and the OPM
memo showing the 2009 COLA factors
is available at https://www.chcoc.gov/
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We note that the COLA areas for
Alaska are not defined by county as are
the COLA areas for Hawaii. In 5 CFR
591.207, the OPM established the
following COLA areas:
• City of Anchorage, and 80-kilometer
(50-mile) radius by road, as measured
from the Federal courthouse.
• City of Fairbanks, and 80-kilometer
(50-mile) radius by road, as measured
from the Federal courthouse.
• City of Juneau, and 80-kilometer
(50-mile) radius by road, as measured
from the Federal courthouse.
• Rest of the state of Alaska.
As stated in the November 2004 IPF
PPS final rule, we update the COLA
factors according to updates established
by the OPM. However, sections 1911
through 1919 of the Non-foreign Area
Retirement Equity Assurance Act, as
contained in subtitle B of title XIX of the
National Defense Authorization Act
(NDAA) (Pub. L. 111–84, October 28,
2009), for FY 2010 transitions the
Alaska and Hawaii COLAs to locality
pay. Under section 1914 of NDAA,
locality pay was phased in over a 3-year
period beginning in January 2010, with
COLA rates frozen as of the date of
enactment, October 28, 2009, and then
proportionately reduced to reflect the
phase-in of locality pay.
When we published the proposed
COLA factors in the RY 2012 IPF PPS
proposed rule (76 FR 4998), we
inadvertently selected the FY 2010
COLA rates, which had been reduced to
account for the phase-in of locality pay.
We did not intend to propose the
reduced COLA rates because that would
have understated the adjustment. Since
the 2009 COLA rates did not reflect the
phase-in of locality pay, we finalized
the FY 2009 COLA rates for RY 2010
through RY 2014.
In the FY 2013 IPPS/LTCH final rule
(77 FR 53700 through 53701), we
established a new methodology to
update the COLA factors for Alaska and
Hawaii and adopted this methodology
for the IPF PPS in the FY 2015 IPF PPS
final rule (79 FR 45958 through 45960).
We adopted this new COLA
methodology for the IPF PPS because
IPFs are hospitals with a similar mix of
commodities and services. We believe it
is appropriate to have a consistent
policy approach with that of other
hospitals in Alaska and Hawaii.
Therefore, the IPF COLAs for FY 2015
through FY 2017 were the same as those
applied under the IPPS in those years.
As finalized in the FY 2013 IPPS/LTCH
PPS final rule (77 FR 53700 and 53701),
the COLA updates are determined every
4 years, when the IPPS market basket
labor-related share is updated. Because
the labor-related share of the IPPS
market basket was updated for FY 2022,
the COLA factors were updated in FY
2022 IPPS/LTCH rulemaking (86 FR
45547). As such, we also updated the
IPF PPS COLA factors for FY 2022 (86
FR 42621 through 42622) to reflect the
updated COLA factors finalized in the
FY 2022 IPPS/LTCH rulemaking. Table
16 shows the IPF PPS COLA factors
effective for FY 2022 through FY 2025.
The IPF PPS COLA factors for FY
2024 are also shown in Addendum A to
this final rule, which is available at
https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
InpatientPsychFacilPPS/tools.html.
ED costs incurred by a psychiatric
hospital with a qualifying ED or an
excluded psychiatric unit of an IPPS
hospital or a CAH, for preadmission
services otherwise payable under the
Medicare Hospital Outpatient
Prospective Payment System (OPPS),
furnished to a beneficiary on the date of
the beneficiary’s admission to the
hospital and during the day
immediately preceding the date of
admission to the IPF (see § 413.40(c)(2)),
and the overhead cost of maintaining
the ED. This payment is a facility-level
adjustment that applies to all IPF
admissions (with one exception, which
we described), regardless of whether a
particular patient receives preadmission
services in the hospital’s ED.
The ED adjustment is incorporated
into the variable per diem adjustment
for the first day of each stay for IPFs
with a qualifying ED. Those IPFs with
a qualifying ED receive an adjustment
factor of 1.31 as the variable per diem
adjustment for day 1 of each patient
stay. If an IPF does not have a qualifying
ED, it receives an adjustment factor of
1.19 as the variable per diem adjustment
for day 1 of each patient stay.
The ED adjustment is made on every
qualifying claim except as described in
4. Adjustment for IPFs With a
Qualifying Emergency Department (ED)
The IPF PPS includes a facility-level
adjustment for IPFs with qualifying EDs.
We provide an adjustment to the
Federal per diem base rate to account
for the costs associated with
maintaining a full-service ED. The
adjustment is intended to account for
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this section of this final rule. As
specified in § 412.424(d)(1)(v)(B), the ED
adjustment is not made when a patient
is discharged from an IPPS hospital or
CAH and admitted to the same IPPS
hospital’s or CAH’s excluded
psychiatric unit. We clarified in the
November 2004 IPF PPS final rule (69
FR 66960) that an ED adjustment is not
made in this case because the costs
associated with ED services are reflected
in the DRG payment to the IPPS hospital
or through the reasonable cost payment
made to the CAH.
Therefore, when patients are
discharged from an IPPS hospital or
CAH and admitted to the same
hospital’s or CAH’s excluded
psychiatric unit, the IPF receives the
1.19 adjustment factor as the variable
per diem adjustment for the first day of
the patient’s stay in the IPF. For FY
2024, we proposed to retain the 1.31
adjustment factor for IPFs with
qualifying EDs. A complete discussion
of the steps involved in the calculation
of the ED adjustment factors are in the
November 2004 IPF PPS final rule (69
FR 66959 through 66960) and the RY
2007 IPF PPS final rule (71 FR 27070
through 27072).
As we did not propose any changes to
the ED adjustment, we are retaining the
existing ED adjustment for FY 2024.
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E. Other Proposed Payment
Adjustments and Policies
1. Outlier Payment Overview
The IPF PPS includes an outlier
adjustment to promote access to IPF
care for those patients who require
expensive care and to limit the financial
risk of IPFs treating unusually costly
patients. In the November 2004 IPF PPS
final rule, we implemented regulations
at § 412.424(d)(3)(i) to provide a per
case payment for IPF stays that are
extraordinarily costly. Providing
additional payments to IPFs for
extremely costly cases strongly
improves the accuracy of the IPF PPS in
determining resource costs at the patient
and facility level. These additional
payments reduce the financial losses
that would otherwise be incurred in
treating patients who require costlier
care, and therefore, reduce the
incentives for IPFs to under-serve these
patients. We make outlier payments for
discharges in which an IPF’s estimated
total cost for a case exceeds a fixed
dollar loss threshold amount
(multiplied by the IPF’s facility-level
adjustments) plus the Federal per diem
payment amount for the case.
In instances when the case qualifies
for an outlier payment, we pay 80
percent of the difference between the
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estimated cost for the case and the
adjusted threshold amount for days 1
through 9 of the stay (consistent with
the median LOS for IPFs in FY 2002),
and 60 percent of the difference for day
10 and thereafter. The adjusted
threshold amount is equal to the outlier
threshold amount adjusted for wage
area, teaching status, rural area, and the
COLA adjustment (if applicable), plus
the amount of the Medicare IPF
payment for the case. We established
the 80 percent and 60 percent loss
sharing ratios because we were
concerned that a single ratio established
at 80 percent (like other Medicare PPSs)
might provide an incentive under the
IPF per diem payment system to
increase LOS in order to receive
additional payments.
After establishing the loss sharing
ratios, we determined the current fixed
dollar loss threshold amount through
payment simulations designed to
compute a dollar loss beyond which
payments are estimated to meet the 2
percent outlier spending target. Each
year when we update the IPF PPS, we
simulate payments using the latest
available data to compute the fixed
dollar loss threshold so that outlier
payments represent 2 percent of total
estimated IPF PPS payments.
2. Update to the Outlier Fixed Dollar
Loss Threshold Amount
In accordance with the update
methodology described in § 412.428(d),
we proposed to update the fixed dollar
loss threshold amount used under the
IPF PPS outlier policy. Based on the
regression analysis and payment
simulations used to develop the IPF
PPS, we established a 2 percent outlier
policy, which strikes an appropriate
balance between protecting IPFs from
extraordinarily costly cases while
ensuring the adequacy of the Federal
per diem base rate for all other cases
that are not outlier cases.
Our longstanding methodology for
updating the outlier fixed dollar loss
threshold involves using the best
available data, which is typically the
most recent available data. For the FY
2022 IPF PPS final rule, we finalized the
use of FY 2019 claims rather than the
more recent FY 2020 claims for
updating the outlier fixed dollar loss
threshold (86 FR 42623). We noted that
our use of the FY 2019 claims to set the
final outlier fixed dollar loss threshold
for FY 2022 deviated from our
longstanding practice of using the most
recent available year of claims but
remained otherwise consistent with the
established outlier update methodology.
We explained that we finalized our
proposal to deviate from our
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longstanding practice of using the most
recent available year of claims only
because, and to the extent that, the
‘‘coronavirus disease 2019’’ (abbreviated
‘‘COVID–19’’) Public Health Emergency
(PHE) appeared to have significantly
impacted the FY 2020 IPF claims. We
further stated that we intended to
continue to analyze further data in order
to better understand both the short-term
and long-term effects of the COVID–19
PHE on IPFs (86 FR 42624).
In the FY 2023 IPF PPS final rule (87
FR 46862 through 46864) we noted that
we observed an overall increase in
average cost per day and an overall
decrease in the number of covered days.
However, we identified that some
providers had significant increases in
their charges, resulting in higher-thannormal estimated cost per day that
would skew our estimate of outlier
payments for FY 2022 and FY 2023. We
finalized our proposal for FY 2023 to
use the latest available FY 2021 claims,
in accordance with our longstanding
practice, to simulate payments for
determining the final FY 2023 IPF PPS
outlier fixed dollar loss threshold
amount. In addition, we finalized a
methodology for FY 2023 to exclude
providers from our impact simulations
whose change in simulated cost per day
is outside 3 standard deviations from
the mean.
For the FY 2024 IPF PPS proposed
rule, consistent with our longstanding
practice, we analyzed the most recent
available data for simulating IPF PPS
payments in FY 2023. Based on an
analysis of these updated data, we
estimated that IPF outlier payments as
a percentage of total estimated payments
were approximately 3.0 percent in FY
2023. We analyzed the change in
providers’ charges from the FY 2021
claims that were used to simulate
payments for determining the final FY
2023 IPF PPS outlier threshold, and the
latest available FY 2022 claims. In
contrast to our analysis of FY 2021
claims for the FY 2023 IPF PPS
proposed and final rules, we did not
find the same level of significant
increases in charges in the FY 2022
claims that we believe would skew our
estimate of outlier payments for FY
2023 and FY 2024. Therefore, we
proposed to update the outlier threshold
amount to $34,750. This would allow us
to maintain estimated outlier payments
at 2 percent of total estimated aggregate
IPF payments for FY 2024. This
proposed update was an increase from
the FY 2023 threshold of $24,630. We
solicited comments on this proposed
increase to the outlier threshold for FY
2024, and whether we should consider
alternative methodologies for FY 2024.
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Specifically, we were interested in
understanding whether commenters
believe it would be appropriate to
exclude providers from our FY 2024
impact simulations whose change in
simulated cost per day is outside 3
standard deviations from the mean,
following the same methodology we
applied in FY 2023. We noted that our
analysis for the FY 2024 proposed rule
showed that the FY 2024 outlier fixed
dollar loss threshold amount would be
closer to $30,000 if we were to exclude
providers based on the same
methodology finalized for FY 2023. We
were also interested in other
methodologies that commenters believe
might be appropriate to consider,
including why commenters believe
applying such a methodology would be
appropriate for establishing the outlier
threshold for FY 2024.
Comment: We received five comments
in response to the FY 2024 IPF PPS
pertaining to an alternative IPF PPS
outlier policy. Commenters included
state-level and national provider
associations. One commenter stated the
increase in the outlier threshold amount
should be limited to no more than the
market basket update for the year but
did not provide a rationale for this
suggestion. Two commenters
recommended CMS mitigate the
financial impact that imperfect outlier
threshold estimates have on IPFs. Four
commenters requested that CMS explain
in greater detail the factors driving the
increase and that CMS examine its
methodology and consider making
changes to mitigate increases to the
outlier threshold. Commenters also
requested information on how the
proposed increase would affect the IPF
field and its patients.
Response: We appreciate the
suggestions from commenters regarding
mitigating the financial impact of the
outlier threshold on IPFs and the use of
alternative methodologies for estimating
the outlier threshold. We are not
finalizing any of the alternative
methodologies that commenters
suggested, but we are providing
additional information about the drivers
and impact of the increase to the outlier
threshold, as commenters requested.
As we previously noted in the FY
2023 final rule (87 FR 46863), we
observed two main trends in the claims
data for FY 2020 and FY 2021. In
summary, these were an increase in
average cost per day and a decrease in
total IPF PPS payments corresponding
with a decrease in covered IPF PPS
days. Both of these trends continued in
the FY 2022 claims data used for this FY
2024 IPF PPS final rule. First, we
observed that average cost per day
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increased approximately 8 percent
when comparing the simulated FY 2022
IPF PPS payments from the FY 2023 IPF
PPS final rule to the simulated FY 2023
IPF PPS payments that we used to
estimate the outlier percentage for this
FY 2024 IPF PPS final rule. In the FY
2022 IPF PPS proposed rule (86 FR
19526), we explained that we estimate
the costs per case based on the covered
charges on each IPF claim and the IPF’s
most recent CCR. The second continued
trend that we observed was that the
number of covered days continued to
decrease in the FY 2022 claims. The
number of covered days in the FY 2022
claims were approximately 12 percent
lower than the number of covered days
in the FY 2021 claims used for FY 2023
final rulemaking, before applying the
statistical trim for the FY 2023 IPF PPS
final rule (87 FR 46862). This decrease
in covered days corresponds with a
decrease of approximately 10 percent in
the total simulated FY 2023 IPF PPS
payments compared to total simulated
FY 2022 IPF PPS payments used for FY
2023 final rulemaking. In addition,
when comparing the data used for this
FY 2024 IPF PPS final rule with the
statistically trimmed data used for the
FY 2023 IPF PPS final rule, the covered
days for FY 2024 were approximately 8
percent lower than FY 2023, and total
simulated FY 2023 IPF PPS payments
that we used to estimate the outlier
percentage for this FY 2024 IPF PPS
final rule were approximately 4 percent
lower than total simulated FY 2022 IPF
PPS payments. Because we calculate the
outlier fixed dollar loss threshold
amount so that outlier payments
represent 2 percent of total estimated
IPF PPS payments, the decrease to the
number of days and total estimated IPF
PPS payments increases the percentage
of outlier payments relative to total
payments, which contributes to the
upward trend in the outlier fixed dollar
loss threshold amount. In our simulated
FY 2023 outlier payments using the FY
2023 IPF PPS outlier fixed dollar loss
threshold of $24,630, we estimated that
5,817 cases will receive outlier
payments, with a mean outlier payment
amount per outlier case of $13,807.28.
We observed that the distribution of
simulated FY 2023 outlier payments is
skewed right, which means that a large
number of outlier cases receive
relatively small amounts of outlier
payments, and a smaller number of
outlier cases receive relatively large
outlier payments. Consequently, half of
all simulated outlier cases receive
outlier payments of $7,543.65 or less,
and 559 cases receive outlier payments
of $1,000 or less. We also observed that
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51091
outlier payments are concentrated
among certain types of IPFs. As shown
in Table 40, in section VIII.C.2 of this
final rule, urban government-owned IPF
units are projected to experience the
largest decreases in estimated payments
as a result of the increase to the outlier
fixed dollar loss threshold amount,
because these providers had a larger
share of outlier cases than other
provider types. We did not observe that
changes in case mix appear to be driving
the increase in the outlier percentage. In
the simulated FY 2023 IPF PPS
payments, we observed that
approximately 79 percent of outlier
cases are for DRG 885 (Psychoses),
which aligns with the proportion of IPF
PPS cases that typically receive that
DRG. We estimate that the average
outlier payment for cases with DRG 885
is $14,485.21, which is comparable to
the average outlier payment for all
cases.
Regarding the suggestion to limit
increases to the outlier threshold to no
more than the market basket update, we
are concerned that this methodology
would not be technically appropriate for
the IPF PPS outlier policy. As discussed
earlier in this section, the longstanding
IPF PPS 2-percent outlier policy was
established based on the regression
analysis and payment simulations used
to develop the IPF PPS. We have
previously explained that the 2-percent
outlier policy strikes an appropriate
balance between protecting IPFs from
extraordinarily costly cases while
ensuring the adequacy of the Federal
per diem base rate for all other cases
that are not outlier cases. Each year
when we update the IPF PPS, we
simulate payments using the latest
available data to compute the fixed
dollar loss threshold so that outlier
payments represent 2 percent of total
estimated IPF PPS payments. For this
FY 2024 IPF PPS final rule, we have
simulated payments using the latest
available data, and these payment
simulations indicate that an increase to
the outlier fixed dollar loss threshold is
necessary in order to maintain outlier
payments at 2 percent of total payments.
We are concerned that limiting
increases to the outlier fixed dollar loss
threshold to no more than the market
basket update percentage would not
appropriately target outlier payments
such that they remain at 2 percent of
total IPF PPS payments and that such a
policy would increase outlier payments
above the 2 percent target for FY 2024.
As we noted in the prior paragraph, we
observe that the increase in the outlier
fixed dollar loss threshold is driven in
part by a continual downward trend in
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covered days over the past several years.
We are concerned that it would not be
appropriate to increase outlier payments
to offset the fact that IPFs are providing
fewer days of care for Medicare
beneficiaries.
Final Decision: After consideration of
the comments received, we are
finalizing our proposal to update the
fixed dollar loss threshold amount used
under the IPF PPS outlier policy. Based
on the latest available data, we are
finalizing an outlier fixed dollar loss
threshold amount of $33,470 for FY
2024.
3. Update to IPF Cost-To-Charge Ratio
Ceilings
Under the IPF PPS, an outlier
payment is made if an IPF’s cost for a
stay exceeds a fixed dollar loss
threshold amount plus the IPF PPS
amount. In order to establish an IPF’s
cost for a particular case, we multiply
the IPF’s reported charges on the
discharge bill by its overall cost-tocharge ratio (CCR). This approach to
determining an IPF’s cost is consistent
with the approach used under the IPPS
and other PPSs. In the FY 2004 IPPS
final rule (68 FR 34494), we
implemented changes to the IPPS policy
used to determine CCRs for IPPS
hospitals, because we became aware
that payment vulnerabilities resulted in
inappropriate outlier payments. Under
the IPPS, we established a statistical
measure of accuracy for CCRs to ensure
that aberrant CCR data did not result in
inappropriate outlier payments.
As indicated in the November 2004
IPF PPS final rule (69 FR 66961), we
believe that the IPF outlier policy is
susceptible to the same payment
vulnerabilities as the IPPS; therefore, we
adopted a method to ensure the
statistical accuracy of CCRs under the
IPF PPS. Specifically, we adopted the
following procedure in the November
2004 IPF PPS final rule:
• Calculated two national ceilings,
one for IPFs located in rural areas and
one for IPFs located in urban areas.
• Computed the ceilings by first
calculating the national average and the
standard deviation of the CCR for both
urban and rural IPFs using the most
recent CCRs entered in the most recent
Provider Specific File (PSF) available.
For FY 2024, we proposed to continue
to follow this methodology.
To determine the rural and urban
ceilings, we multiplied each of the
standard deviations by 3 and added the
result to the appropriate national CCR
average (either rural or urban). The
upper threshold CCR for IPFs in FY
2024 is 2.1419 for rural IPFs, and 1.8026
for urban IPFs, based on CBSA-based
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geographic designations. If an IPF’s CCR
is above the applicable ceiling, the ratio
is considered statistically inaccurate,
and we assign the appropriate national
(either rural or urban) median CCR to
the IPF.
We apply the national median CCRs
to the following situations:
• New IPFs that have not yet
submitted their first Medicare cost
report. We continue to use these
national median CCRs until the facility’s
actual CCR can be computed using the
first tentatively or final settled cost
report.
• IPFs whose overall CCR is in excess
of three standard deviations above the
corresponding national geometric mean
(that is, above the ceiling).
• Other IPFs for which the Medicare
Administrative Contractor (MAC)
obtains inaccurate or incomplete data
with which to calculate a CCR.
We proposed to update the FY 2024
national median and ceiling CCRs for
urban and rural IPFs based on the CCRs
entered in the latest available IPF PPS
PSF.
Specifically, for FY 2024, to be used
in each of the three situations listed
previously, using the most recent CCRs
entered in the CY 2022 PSF, we
provided an estimated national median
CCR of 0.5720 for rural IPFs and a
national median CCR of 0.4200 for
urban IPFs. These calculations are based
on the IPF’s location (either urban or
rural) using the CBSA-based geographic
designations. A complete discussion
regarding the national median CCRs
appears in the November 2004 IPF PPS
final rule (69 FR 66961 through 66964).
4. Modification to the Regulation for
Excluded Psychiatric Units Paid Under
the IPF PPS
a. Background
Under current regulation, in order to
be excluded from the IPPS and paid
under the IPF PPS or the IRF PPS, an
IPF or IRF unit of a hospital must meet
a number of requirements under 42 CFR
412.25. As discussed in the following
paragraphs, both this regulation and the
policies applying to excluded units
(which include excluded IRF units and
excluded IPF units) have been in effect
since before both the IPF PPS and IRF
PPS were established. Before the IRF
PPS and the IPF PPS were established,
excluded units were paid based on their
costs, as reported on their Medicare cost
reports, subject to certain facilityspecific cost limits. These cost-based
payments were determined separately
for operating and capital costs. Thus,
under cost-based payments, the process
of allocating costs to an IPF unit for
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reimbursement created significant
administrative complexity. This
administrative complexity necessitated
strict regulations that allowed hospitals
to open a new IPPS-excluded unit only
at the start of a cost reporting period.
In the January 3, 1984 final rule (49
FR 235), CMS (then known as the
Health Care Financing Administration)
established policies and regulations for
hospitals and units subject to and
excluded from the IPPS. In that rule, we
explained that section 1886(d) of the
Act requires that the prospective
payment system apply to inpatient
hospital services furnished by all
hospitals participating in the Medicare
program except those hospitals or units
specifically excluded by the law. We
further explained our expectation that a
hospital’s status (that is, whether it is
subject to, or excluded from, the
prospective payment system) would
generally be determined at the
beginning of each cost reporting period.
We also stated that this status would
continue throughout the period, which
is normally 1 year. Accordingly, we
stated that changes in a hospital’s (or
unit’s) status that result from meeting or
failing to meet the criteria for exclusion
would be implemented only at the start
of a cost reporting period. However, we
also acknowledged that under some
circumstances involving factors external
to the hospital, status changes could be
made at times other than the beginning
of the cost reporting period. For
example, a change in status could occur
if a hospital is first included under the
prospective payment system and, after
the start of its cost reporting period, is
excluded because of its participation in
an approved demonstration project or
State reimbursement control program
that begins after the hospital’s cost
reporting period has begun.
In the 1993 IPPS final rule (57 FR
39798 through 39799), we codified our
longstanding policies regarding when a
hospital unit can change its status from
not excluded to excluded. We explained
in that final rule that since the inception
of the PPS for operating costs of hospital
inpatient services in October 1983,
certain types of specialty-care hospitals
and hospital units have been excluded
from that system under section
1888(d)(1)(B) of the Act. We noted that
these currently include psychiatric and
rehabilitation hospitals and distinct part
units, children’s hospitals, and longterm care hospitals. We further
explained that section 6004(a)(1) of
Public Law 101–239 amended section
1886(d)(1)(B) of the Act to provide that
certain cancer hospitals are also
excluded. We noted that the preamble to
the January 3, 1984 final rule
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implementing the PPS for operating
costs (49 FR 235) stated that the status
of a hospital or unit (that is, whether it
is subject to, or excluded from, the PPS)
will be determined at the beginning of
each cost reporting period. We noted
that that same 1984 final rule also
provided that changes in a hospital’s or
unit’s status that result from meeting or
failing to meet the criteria for exclusion
will be implemented prospectively only
at the start of a cost reporting period,
that is, starting with the beginning date
of the next cost reporting period (49 FR
243). However, we noted that this policy
was not set forth in the regulations. In
that 1993 IPPS final rule, we stated that
we proposed revising §§ 412.22 and
412.25 to specify that changes in the
status of each hospital or hospital unit
would be recognized only at the start of
a cost reporting period. We stated that,
except in the case of retroactive
payment adjustments for excluded
rehabilitation units described in
§ 412.30(c), any change in a hospital’s or
unit’s compliance with the exclusion
criteria that occurs after the start of a
cost reporting period would not be
taken into consideration until the start
of the following period. We noted that
this policy would also apply to any unit
that is added to a hospital during the
hospital’s cost reporting period. We also
stated that we proposed revising
§ 412.25(a) to specify that as a
requirement for exclusion, a hospital
unit must be fully equipped and staffed,
and be capable of providing inpatient
psychiatric or rehabilitation care as of
the first day of the first cost reporting
period for which all other exclusion
requirements are met. We explained that
a unit that meets this requirement
would be considered open regardless of
whether there are any inpatients in the
unit.
In the same 1993 IPPS final rule, we
responded to commenters who objected
to this policy, stating that it
unnecessarily penalizes hospitals for
factors beyond their control, such as
construction delays, that it discourages
hospitals from making changes in their
programs to meet community needs, or
that it can place undue workload
demands on regulatory agencies during
certain time periods. In response, we
explained that we believed that
regulatory agencies, hospitals, and the
public generally would benefit from
policies that are clearly stated, can be
easily understood by both hospitals and
intermediaries, and can be simply
administered. We stated that
recognizing changes in status only at the
beginning of cost reporting periods is
consistent with these goals, while
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recognizing changes in the middle of
cost reporting periods would introduce
added complexity to the administration
of the exclusion provisions. Therefore,
we did not revise the proposed changes
based on these comments.
In the FY 2000 IPPS final rule (64 FR
41531 through 41532), we amended the
regulations at § 412.25(c) to allow a
hospital unit to change from excluded to
not excluded at any time during the cost
reporting period. We explained the
statutory basis and rationale for this
change in the FY 2000 IPPS proposed
rule (64 FR 24740) and noted that a
number of hospitals suggested that we
consider a change in our policy to
recognize, for purposes of exclusion
from the IPPS, reductions in number of
beds in, or entire closure of, units at any
time during a cost reporting period. In
that FY 2000 IPPS proposed rule, we
explained that hospitals indicated that
the bed capacity made available as a
result of these changes could be used as
needed to provide additional services to
meet patient needs in the acute care part
of the hospital that is paid under the
IPPS. We further explained that we
evaluated the concerns of the hospitals
and the effects on the administration of
the Medicare program and the health
care of beneficiaries of making these
payment changes. As a result of that
evaluation, we stated that we believed it
was reasonable to adopt a more flexible
policy in recognition of hospitals’
changes in the use of their facilities.
However, we noted that whenever a
hospital establishes an excluded unit
within the hospital, our Medicare fiscal
intermediary would need to be able to
determine costs of the unit separately
from costs of the part of the hospital
paid under the prospective payment
system. At that time, we stated that the
proper determination of costs ensured
that the hospital was paid the correct
amount for services in each part of the
facility, and that payments under the
IPPS did not duplicate payments made
under the rules that were applicable to
excluded hospitals and units, or vice
versa. For this reason, we did not
believe it would be appropriate to
recognize, for purposes of exclusion
from the IPPS, changes in the bed size
or status of an excluded unit that are so
frequent that they interfere with the
ability of the intermediary to accurately
determine costs. Moreover, we
explained that section 1886(d)(1)(B) of
the Act authorizes exclusion from the
IPPS of specific types of hospitals and
units, but not of specific admissions or
stays, such as admissions for
rehabilitation or psychiatric care, in a
hospital paid under the IPPS. We stated
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that without limits on the frequency of
changes in excluded units for purposes
of proper Medicare payment, there was
the potential for some hospitals to
adjust the status or size of their
excluded units so frequently that the
units would no longer be distinct
entities and the exclusion would
effectively apply only to certain types of
care.
In the FY 2012 IRF PPS final rule (76
FR 47870), we began further efforts to
increase flexibilities for excluded IPF
and IRF units. In that rule, we explained
that cost-based reimbursement
methodologies that were in place before
the IPF PPS and IRF PPS meant that the
facilities’ capital costs were determined,
in part, by their bed size and square
footage. Changes in the bed size and
square footage would complicate the
facilities’ capital cost allocation. Thus,
regulations at § 412.25 limited the
situations under which an IRF or IPF
could change its bed size and square
footage. In the FY 2012 IRF PPS final
rule, we revised § 412.25(b) to enable
IRFs and IPFs to more easily adjust to
beneficiary changes in demand for IRF
or IPF services and improve beneficiary
access to these services. We believed
that the first requirement (that beds can
only be added at the start of a cost
reporting period) was difficult, and
potentially costly, for IRFs and IPFs that
were expanding through new
construction because the exact timing of
the end of a construction project is often
difficult to predict. In that same FY
2012 IRF PPS final rule, commenters
suggested that CMS allow new IRF units
or new IPF units to open and begin
being paid under their respective IRF
PPS or IPF PPS at any time during a cost
reporting period, rather than requiring
that they could only begin being paid
under the IRF PPS or the IPF PPS at the
start of a cost reporting period. We
believed that this suggestion was
outside the scope of the FY 2012 IRF
PPS proposed rule (76 FR 24214),
because we did not propose any changes
to the § 412.25(c). However, we stated
that we would consider this suggestion
for possible inclusion in future
rulemaking.
b. Current Challenges Related to
Excluded Hospital Units (§§ 412.25(c)(1)
and (c)(2))
Currently, under § 412.25(c)(1), a
hospital can only start being paid under
the IPF PPS or the IRF PPS for services
provided in an excluded hospital unit at
the start of a cost reporting period.
Specifically, § 412.25(c) limits when the
status of hospital units may change for
purposes of exclusion from the IPPS, as
specified in §§ 412.25(c)(1) and
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412.25(c)(2). Section 412.25(c)(1) states
that the status of a hospital unit may be
changed from not excluded to excluded
only at the start of the cost reporting
period. If a unit is added to a hospital
after the start of a cost reporting period,
it cannot be excluded from the IPPS
before the start of a hospital’s next cost
reporting period. Section 412.25(c)(2)
states the status of a hospital unit may
be changed from excluded to not
excluded at any time during a cost
reporting period, but only if the hospital
notifies the fiscal intermediary and the
CMS Regional Office in writing of the
change at least 30 days before the date
of the change, and maintains the
information needed to accurately
determine costs that are or are not
attributable to the excluded unit. A
change in the status of a unit from
excluded to not excluded that is made
during a cost reporting period must
remain in effect for the rest of that cost
reporting period.
In recent years, interested parties,
such as hospitals, have written CMS to
express concerns about what they see as
the unnecessary restrictiveness of the
requirements at § 412.25(c). Based on
this feedback, we continued to explore
opportunities to reduce burden for
providers and clinicians, while keeping
patient-centered care a priority. For
instance, we considered whether this
regulation might create unnecessary
burden for hospitals and potentially
delay necessary psychiatric beds from
opening and being paid under the IPF
PPS. As we continued to review and
reconsider regulations to identify ways
to improve policy, we recognized that
the requirement at § 412.25(c)(1), that
hospital units can only be excluded at
the start of a cost reporting period, may
be challenging and potentially costly for
facilities under some circumstances, for
example, those that are expanding
through new construction. Hospitals
have indicated it is often difficult to
predict the exact timing of the end of a
construction project and construction
delays may hamper a hospital’s ability
to have the construction of an excluded
unit completed exactly at the start of a
cost reporting period, which hospitals
have said can lead to significant revenue
loss if they are unable to be paid under
the IPF PPS or IRF PPS until the start
of the next cost reporting period.
As previously stated, the
requirements at § 412.25(c) were
established to manage the
administrative complexity associated
with cost-based reimbursement for
excluded IPF and IRF units. Today,
however, because IPF units are paid
under the IPF PPS and IRF units are
paid under the IRF PPS, cost allocation
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is not used for payment purposes.
Because advancements in technology
since the inception of the IPF PPS and
IRF PPS have simplified the cost
reporting process and enhanced
communication between providers,
Medicare contractors, and CMS, we are
reconsidering whether it is necessary to
continue to allow hospital units to
become excluded only at the start of a
cost reporting period.
c. Changes to Excluded Hospital Units
(§§ 412.25(c)(1) and (c)(2))
We are committed to continuing to
transform the health care delivery
system and the Medicare program by
putting additional focus on patientcentered care and working with
providers, physicians, and patients to
improve outcomes, while meeting
relevant health care priorities and
exploring burden reduction.
In response to increased mental
health needs, including the need for
availability of inpatient psychiatric
beds, we proposed changes to
§ 412.25(c) to allow greater flexibility for
hospitals to open excluded units, while
minimizing the amount of effort
Medicare contractors would need to
spend administering the regulatory
requirements. Although we are
cognizant that there is need for mental
health services and support for
providers along a continuum of care,
including a robust investment in
community-based mental health
services, this proposal was focused on
inpatient psychiatric facility settings.
We proposed that changes to
§ 412.25(c) would apply to both IPFs
and IRFs; therefore, revisions to
§ 412.25(c) would also affect IRFs in
similar ways. Readers should refer to
the FY 2024 IRF PPS proposed rule (88
FR 20981 through 20984) for discussion
of proposed revisions to § 412.25(c) and
unique considerations applicable to IRF
units. As previously stated, the current
requirements at § 412.25(c)(1) were
originally established to manage the
administrative complexity associated
with cost-based reimbursement for
excluded IPF and IRF units. Because IPF
and IRF units are no longer paid under
cost-based reimbursement, but rather
under the IPF PPS and IRF PPS
respectively, we believe that the
restriction that limits an IPF or IRF unit
to being excluded only at the start of a
cost reporting period is no longer
necessary. We amended our regulations
in the FY 2012 IRF PPS final rule to
address a regulation that, similarly, was
previously necessary for cost-based
reimbursement, but was not material to
payment under the IRF PPS and IPF
PPS. In that final rule, we explained that
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under cost-based payments, the
facilities’ capital costs were determined,
in part, by their bed size and square
footage. Changes in the bed size and
square footage would complicate the
facilities’ capital cost allocation. We
explained that under the IRF PPS and
IPF PPS, a facility’s bed size and square
footage were not relevant for
determining the individual facility’s
Medicare payment. Therefore, we
believed it was appropriate to modify
some of the restrictions on a facility’s
ability to change its bed size and square
footage. Accordingly, we relaxed the
restrictions on a facility’s ability to
increase its bed size and square footage.
Under the revised requirements that we
adopted in the FY 2012 IRF PPS final
rule at § 412.25(b), an IRF or IPF can
change (either increase or decrease) its
bed size or square footage one time at
any point in a given cost reporting
period as long as it notifies the CMS
Regional Office (RO) at least 30 days
before the date of the proposed change,
and maintains the information needed
to accurately determine costs that are
attributable to the excluded units.
Similarly, in the case of the
establishment of new excluded IPF and
IRF units, we do not believe that the
timing of the establishment of the new
unit is material for determining the
individual facility’s Medicare payment
under the IPF PPS or IRF PPS. We
believe it would be appropriate to allow
a unit to become excluded at any time
in the cost reporting year. However, we
also believe it is important to minimize
the potential administrative complexity
associated with units changing their
excluded status.
Accordingly, we proposed to modify
the requirements currently in regulation
at § 412.25(c)(1) to allow a hospital to
change the status of an IPF unit any
time within the cost reporting year, as
long as the hospital notifies the CMS
Regional Office and Medicare
Administrative Contractor (MAC) in
writing of the change at least 30 days
before the date of the change, and that
this change would remain in effect for
the rest of that cost reporting year. We
also proposed to maintain the current
requirements of § 412.25(c)(2) which
specify that, if an excluded unit
becomes not excluded during a cost
reporting year, the hospital must notify
the MAC and CMS Regional Office in
writing of the change at least 30 days
before the change, and this change
would remain in effect for the rest of
that cost reporting year. Finally, we
proposed to consolidate the
requirements for § 412.25(c)(1) and
§ 412.25(c)(2) into a new § 412.25(c)(2)
that would apply to IPF units and
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specify the requirements for an IPF unit
to become excluded or not excluded.
We stated that we believed this proposal
would provide greater flexibility to
hospitals to establish an excluded unit
at a time other than the start of a cost
reporting period. We solicited
comments on the proposed changes.
Comment: We received unanimous
commenter support on the proposal to
modify the requirements to allow a
hospital to open a new IPF unit any
time within the cost reporting year, as
long as the hospital notifies the CMS
Regional Office and MAC in writing of
the change at least 30 days before the
date of the change. Commenters were
appreciative of how this change would
allow greater flexibility in how and
when a unit could be designated to be
excluded or not from the IPPS.
Commenters also stated this change
could alleviate the problem of limited
bed availability by allowing hospitals to
be more responsive to the need for
inpatient psychiatric beds in their
communities.
Response: We thank commenters for
their support and agree this
modification will allow greater
flexibility in how and when a unit could
be designated to be excluded from the
IPPS. We also agree this change will
allow hospitals to be more responsive to
the need for inpatient psychiatric beds.
Comment: One commenter requested
that CMS allow certain units that have
changed their status to change their
status back at least one time during the
same cost reporting period. Specifically,
they believe that units that experience a
status change on the first day of the cost
reporting period should have the
opportunity to revert to their original
designation one time throughout the
cost reporting period. They further
clarified that, if an IPF unit specifies
and communicates with the appropriate
parties before the beginning of the next
cost reporting year that it would want to
reclassify, and then when the cost
reporting period begins decides to
revert, it should be allowed the
opportunity to make the necessary
changes.
Response: We do not fully understand
the commenter’s concern, but we
believe the commenter is seeking
clarification about whether a hospital
unit would be permitted to change its
status during the cost reporting year to
revert to the status it held during the
prior year. Under the proposed policy,
a hospital unit would be permitted to
change its status to either excluded or
not excluded only one time during the
cost reporting year, and would be
required to maintain that status until the
end of the cost reporting year. We are
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clarifying that changes made at the
beginning of a cost reporting year would
not limit the ability of the hospital unit
to make a one-time status change during
the same cost reporting year. Therefore,
if the hospital unit starts the cost
reporting year as excluded, it could
become not excluded at any time during
the cost reporting year; if the hospital
unit starts the cost reporting year as not
excluded, it could become excluded at
any time during the cost reporting year.
Final Decision: After consideration of
the comments received, we are
finalizing our proposal to modify the
requirements currently in regulation at
§ 412.25(c)(1) to allow a hospital to
change the status of an IPF unit from not
excluded to excluded any time within
the cost reporting year. We are also
finalizing as proposed that a hospital
will be required to notify the CMS
Regional Office and MAC in writing of
the change at least 30 days before the
date of the change, and that this change
would remain in effect for the rest of
that cost reporting year. In addition, we
are finalizing our proposal to maintain
the current requirements of
§ 412.25(c)(2), which specify that, if an
excluded unit becomes not excluded
during a cost reporting year, the hospital
must notify the MAC and CMS Regional
Office in writing of the change at least
30 days before the change, and this
change would remain in effect for the
rest of that cost reporting year.
Lastly, we proposed an identical
policy for rehabilitation units of
hospitals in the FY 2024 IRF PPS
proposed rule, specifying that the
regulatory provision that would pertain
to IRF units would appear in
§ 412.25(c)(1). We proposed discrete
regulation text for each of the hospital
unit types (that is, IRF units and IPF
units) in order to solicit comments on
issues that might impact one hospital
unit type and not the other. We also
stated that we may consider adopting
one consolidated regulations text for
both IRF and IPF units in the final rules
if we finalize both of our proposals. We
did not receive any comments regarding
a consolidated regulation for both IRF
and IPF units; nor did commenters raise
any issues that would impact one
hospital unit type and not the other. We
are finalizing a consolidated regulation
at § 412.25(c) that applies to both IPF
hospital units and IRF hospital units.
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V. Existing Data Collection and Request
for Information (RFI) To Inform
Revisions to the IPF PPS as Required by
the CAA, 2023
A. Changes to IPF PPS in the CAA, 2023
As discussed in section IV.C.1 of this
final rule, we proposed to continue
using the existing regression-derived
IPF PPS adjustment factors for FY 2024.
In the FY 2023 IPF PPS proposed rule
(87 FR 19428 through 19429), we
discussed the background of these
current IPF PPS patient-level and
facility-level adjustment factors, which
are the regression-derived adjustment
factors from the November 15, 2004 IPF
PPS final rule and briefly discussed past
analyses and areas of concern for future
refinement, about which we previously
solicited comments. Finally, in the FY
2023 proposed rule, we described the
results of the latest analysis of the IPF
PPS, which were summarized in a
technical report posted to the CMS
website 3 accompanying the rule and
solicited comments on certain topics
from the report.
Section 4125 of the CAA, 2023
amended section 1886(s) of the Act to
add new paragraph 1886(s)(5), which
requires revisions to the methodology
for determining the payment rates under
the IPF PPS for FY 2025 and future
years as the Secretary determines
appropriate. Specifically, new section
1886(s)(5)(A) of the Act requires the
Secretary to collect data and
information as the Secretary as
determines appropriate to revise
payments under the IPF PPS. This data
collection is required to begin no later
than October 1, 2023, which is the start
of FY 2024. In addition, new section
1886(s)(5)(D) of the Act requires that the
Secretary implement by regulation
revisions to the methodology for
determining the payment rates for
psychiatric hospitals and psychiatric
units (that is, under the IPF PPS), for
rate year 2025 (FY 2025) and for
subsequent years if the Secretary
determines it appropriate. The revisions
may be based on a review of the data
and information collection.
As noted above, section 1886(s)(5)(A)
of the Act requires the Secretary to
begin collecting, by not later than
October 1, 2023, data and information as
appropriate to inform revisions to the
IPF PPS. New section 1886(s)(5)(B) of
the Act, as added by the CAA, 2023 lists
the following types of data and
information as a non-exhaustive list of
3 https://www.cms.gov/files/document/technicalreport-medicare-program-inpatient-psychiatricfacilities-prospective-payment-system.pdf.
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examples of what may be collected
under this authority:
• Charges, including those related to
ancillary services;
• The required intensity of behavioral
monitoring, such as cognitive deficit,
suicidal ideations, violent behavior, and
need for physical restraint; and
• Interventions, such as
detoxification services for substance
abuse, dependence on respirator, total
parenteral nutritional support,
dependence on renal dialysis, and burn
care.
We note that our extensive years-long
and ongoing data collection efforts are
consistent with the types of data the
CAA, 2023 suggests we might collect as
well as the purpose for which the CAA,
2023 requires the data collection, as
described in the following paragraphs.
B. Current Data and Information
Collection Requirements
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1. Charges, Including Those Related to
Ancillary Services
As specified at 42 CFR 413.20,
hospitals are required to file cost reports
on an annual basis and maintain
sufficient financial records and
statistical data for proper determination
of costs payable under the Medicare
program. Currently, IPFs and
psychiatric units are required to report
ancillary charges on cost reports.
In general, most providers allocate
their Medicare costs using costs and
charges as described at 42 CFR
413.53(a)(1)(i) and referred to as the
Departmental Method. For cost
reporting periods beginning on or after
October 1, 1982, the Departmental
Method, which is the ratio of
beneficiary charges to total patient
charges for the services of each ancillary
department, is applied to apportion the
cost of the department. Added to this
amount is the cost of routine services for
program beneficiaries, determined on
the basis of a separate average cost per
diem for all patients for general routine
patient care areas as required at
§ 413.53(a)(1)(i) and (e).
The Departmental Method for
apportioning allowable cost between
Medicare and non-Medicare patients
under the program is not readily
adaptable to those hospitals that do not
have a charge structure. Current cost
reporting rules allow hospitals that do
not have a charge structure to file an allinclusive cost report using an
alternative cost allocation method.
These alternative methods as described
in the CMS Pub. 15–1, chapter 22 of the
Provider Reimbursement Manual (PRM),
Methods A, B and E, in order of
preference, must be approved by the
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MAC after considering the data
available and ascertaining which
method can be applied to achieve
equity, not merely greater
reimbursement, in the allocation of
costs for services rendered to Medicare
beneficiaries.
Method A (Departmental Statistical
Method) is used in the absence of charge
data and where adequate departmental
statistics are available. Where Method A
was not used, the MAC may have
granted specific permission for a
hospital to continue to use on a
temporary basis a less sophisticated
Method B (Sliding Scale) or E
(Percentage of Per Diem). A provider
that elects and is approved under
Method A, may not change to a Method
B or E in a subsequent year. These
alternative methods of apportionment
are limited and available only to those
hospitals that do not and never have
had a charge structure for individual
services rendered. Historically, most
hospitals that were approved to file allinclusive cost reports were Indian
Health Services hospitals, governmentowned psychiatric and acute care
hospitals, and nominal charge hospitals.
In the FY 2016 IPF PPS final rule (80
FR 46693 through 46694), we discussed
analysis conducted to better understand
IPF industry practices for future IPF PPS
refinements. This analysis revealed that
in 2012 to 2013, over 20 percent of IPF
stays show no reported ancillary costs,
such as laboratory and drug costs, on
cost reports or charges on claims. In the
FY 2016 IPF PPS final rule (80 FR
46694), FY 2017 IPF PPS final rule (81
FR 50513), FY 2018 IPF PPS final rule
(82 FR 36784), FY 2019 IPF PPS final
rule (83 FR 38588) and FY 2020 IPF PPS
final rule (84 FR 38458), we reminded
providers that we pay only the IPF for
services furnished to a Medicare
beneficiary who is an inpatient of that
IPF, except for certain professional
services, and payments are considered
to be payments in full for all inpatient
hospital services provided directly or
under arrangement (see 42 CFR
412.404(d)), as specified in 42 CFR
409.10.
On November 17, 2017, we issued
Transmittal 12, which made changes to
the hospital cost report form CMS–
2552–10 (OMB No. 0938–0050), and
included cost report Level I edit 10710S,
effective for cost reporting periods
ending on or after August 31, 2017. Edit
10710S required that cost reports from
psychiatric hospitals include certain
ancillary costs, or the cost report will be
rejected. On January 30, 2018, we issued
Transmittal 13, which changed the
implementation date for Transmittal 12
to be for cost reporting periods ending
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on or after September 30, 2017. CMS
suspended edit 10710S effective April
27, 2018, pending evaluation of the
application of the edit to all-inclusiverate providers. CMS issued Transmittal
15 on October 19, 2018, reinstating the
requirement that cost reports from
psychiatric hospitals, except allinclusive rate providers, include certain
ancillary costs. For details, we refer
readers to see these Transmittals, which
are available on the CMS website at
https://www.cms.gov/regulations-andguidance/guidance/transmittals.
2. Required Intensity of Behavioral
Monitoring and Interventions
As discussed in the November 2004
IPF PPS final rule (69 FR 66946), we
encourage IPFs to code all diagnoses
requiring active treatment during the
IPF stay. These include ICD–10–CM
codes that indicate the required
intensity of behavioral monitoring, such
as cognitive deficit, suicidal ideations,
violent behavior, and need for physical
restraint. The IPF PPS includes
comorbidity and MS–DRG adjustment
factors that increase IPF PPS payment
for stays that include these codes. For
example, ICD–10–CM codes X71
through X83 indicate self-harm. ICD–
10–CM codes under R45 indicate
emotional state including violent
behavior. These and other ICD–10–CM
codes indicate the required intensity of
behavioral monitoring and should be
reported on the IPF claims, if
applicable.
The presence of certain ICD–10–CM
codes as a principal or comorbid
condition is used to adjust IPF PPS
payments to reflect the resource
intensity associated with these
conditions. For example, codes that
group to MS–DRG 884 Organic
Disturbances & Intellectual Disabilities,
and codes that are included in the IPF
comorbidity category for Developmental
Disabilities, result in increased payment
for IPF stays for patients with cognitive
deficit.
As we further discussed in the
November 2004 IPF PPS final rule (69
FR 66938 through 66944), we developed
comorbidity categories based on the
clinical expertise of physicians to
identify conditions that would require
comparatively more costly treatment
during an IPF stay than other comorbid
conditions. We used a regression
analysis of administrative claims and
cost report data to determine the
adjustment factors associated with each
comorbidity category. In addition, we
used the same regression analysis to
determine the adjustment factors
associated with the 17 MS–DRGs that
are included for payment adjustments
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under the IPF PPS (as identified in
Addendum A). As discussed in section
IV.C.2.b of this final rule, we routinely
update the ICD–10–CM codes that are
included in the MS–DRGs and
comorbidity categories.
We also collect relevant demographic
information such as patient age, and we
collect information and adjust payment
based on the length of IPF stays. Each
of these adjustments reflects the
difference in service intensity, as
measured by increased or decreased
costs, for different patients over the
course of an IPF stay.
In addition, IPFs and psychiatric units
report on claims the ICD–10–PCS codes
for interventions including oncology
treatment procedures, which is used for
adjusting payment under the oncology
comorbidity category, and ECT, which
is paid for using a per treatment amount
as discussed in section IV.B.2 of this
final rule. Other ICD–10–CM diagnosis
codes indicate the need for certain
interventions, such as detoxification
services or substance abuse (for
example, F10.121, which is included in
the drug and alcohol abuse comorbidity
category), dependence on respirator (for
example, Z99.11 included in the COPD
category), and dependence on renal
dialysis (for example, Z99.2 included in
the chronic renal failure category). We
note that the IPS PPF does not currently
adjust for burn care but recognize there
are ICD–10–CM/PCS codes that denote
conditions and procedures related to
burn care. As discussed in the previous
paragraph, the IPF PPS includes
comorbidity adjustments that reflect the
higher relative costs for active treatment
of these conditions. IPF patients with
these conditions are costlier to treat
primarily because of the costs associated
with interventions and longer lengths of
stay.
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3. Request for Information on Data and
Information Collection
As noted in section V.A of this final
rule, our extensive years-long and
ongoing data collection efforts are
consistent with the types of data that the
CAA, 2023 suggests we might collect, as
well as aligns with the purpose for
which the CAA, 2023 requires the data
collection. In this final rule, we are
requesting information from the public
to inform revisions to the IPF PPS
required by section 4125(a) of the CAA,
2023. We are seeking information about
specific additional data and information
psychiatric hospitals and psychiatric
units might report that could be
appropriate and useful to help inform
possible revisions to the methodology
for payment rates under the IPF PPS for
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FY 2025 and future years if determined
appropriate by the Secretary.
Section 1886(s)(5)(C) of the Act
provides that the Secretary may collect
additional data and information on cost
reports, claims, or otherwise. Therefore,
we also sought information about
potential available data and information
sources, including using additional
elements of the current cost reports,
claims, or other sources, taking into
consideration factors such as the timing
and availability of data, the quality of
the potential data and information to be
collected, and the potential
administrative burden on providers,
MACs, and CMS.
We solicited comment on the
following topics:
• What other data and information
would be beneficial for informing
revisions to the IPF PPS payment
methodologies that are currently
obtainable through claims or cost report
information? What codes, conditions, or
other indicators should we examine in
order to potentially identify this data
from existing sources?
• What other data and information
would be beneficial for informing
revisions to the IPF PPS payment
methodologies that are not routinely
coded on claims or identifiable through
cost report information? What are some
potential alternative sources we could
consider for collecting these data and
information?
• What data and information that is
currently reported on claims data could
be used to inform revisions to the IPF
PPS payment methodologies?
• As we discussed in the FY 2024 IPF
PPS proposed rule, the current IPF PPS
payment adjustments were derived from
a regression analysis based on the FY
2002 MedPAR data file. The adjustment
factors included for payment were
found in the regression analysis to be
associated with statistically significant
per diem cost differences; with
statistical significance defined as p less
than 0.05. Are there alternative
methodological approaches or
considerations that we should consider
for future analysis?
• What if any additional data or
information should we consider
collecting that could address access to
care in rural and isolated communities?
4. Request for Information About
Charges for Ancillary Services
In conjunction with the FY 2023 IPF
PPS proposed rule (87 FR 19428
through 19429), we posted a report on
the CMS website that summarizes the
results of the latest analysis of more
recent IPF cost and claim information
for potential IPF PPS adjustments and
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requested comments about the results
summarized in the report. That report
showed that approximately 23 percent
of IPF stays were trimmed from the data
set used in that analysis because they
were stays at facilities where fewer than
5 percent of their stays had ancillary
charges. This report is available online
at https://www.cms.gov/medicare/
inpatient-psychiatric-facility-pps/ipfreports-and-educational-resources.
In response to the comment
solicitation, we received a comment
from MedPAC regarding facilities that
do not report ancillary charges on most
or any of their claims. Ancillary services
are the services for which charges are
customarily made in addition to routine
services. These include services such as
labs, drugs, radiology, physical and
occupational therapy services, and other
types of services that typically vary
between stays. Generally, based on the
nature of IPF services and the
conditions of participation 4 applicable
to IPFs, we expect to see ancillary
services and correlating charges, such as
labs and drugs, on most IPF claims. Our
ongoing analysis has found that certain
providers, especially for-profit
freestanding IPFs, are consistently
reporting no ancillary charges or very
minimal ancillary charges. MedPAC
stated that it is not known: whether IPFs
fail to report ancillary charges
separately because they were
appropriately bundled with all other
charges into an all-inclusive per diem
rate; if no ancillary charges were
incurred because the IPF cares for a
patient mix with lower care needs or
inappropriately stints on care; or if
ancillary charges for services furnished
during the IPF stay are inappropriately
billed outside of the IPF base rate
(unbundling). MedPAC recommended
CMS conduct further investigation into
the lack of certain ancillary costs and
charges and whether IPFs are providing
necessary care and appropriately billing
for inpatient psychiatric services under
the IPF PPS.
As discussed in the previous section
of this FY 2024 IPF PPS final rule, we
requested information related to the
specific types of data and information
specified in the CAA, 2023, including
the reporting of charges for ancillary
services, such as labs and drugs, on IPF
claims. We are interested in better
understanding IPF industry practices
4 IPFs are subject to all hospital conditions of
participation, including 42 CFR 482.25, which
specifies that ‘‘The hospital must have
pharmaceutical services that meet the needs of the
patients,’’ and 482.27, which specifies that ‘‘The
hospital must maintain, or have available, adequate
laboratory services to meet the needs of its
patients.’’
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pertaining to the billing and provision
of ancillary services to inform future IPF
PPS refinements. We are considering
whether to require charges for ancillary
services to be reported on claims and
potentially reject claims if no ancillary
services are reported, and whether to
consider payment for such claims to be
inappropriate or erroneous and subject
to recoupment. Accordingly, we
solicited comments on the following
questions:
• What would be the appropriate
level of ancillary charges CMS should
expect to be reported on claims? Are
there specific reasons that an IPF stay
would include no ancillary services?
• What are the reasons that some
providers are not reporting ancillary
charges on their claims?
• Would it be appropriate for CMS to
require and reject claims if there are no
ancillary charges reported? Or should
CMS consider adjusting payment to
providers that do not report ancillary
charges on their claims? For example,
does the lack of ancillary charges on
claims suggest a lack of reasonable and
necessary treatment during the IPF stay,
and would it be appropriate for CMS to
only apply the IPF PPS patient-level
adjustment factors for claims that
include ancillary charges?
C. Social Drivers of Health
Social drivers of health (SDOH), also
known as social determinants of health,
are the conditions in the environments
where people are born, live, learn, work,
play, worship, and age that affect a wide
range of health, functioning, and
quality-of-life outcomes and risks.5
Studies have shown that there is a
correlation between the effects of low
income and education and overall
health status. One study derived that the
lowest income and least educated
individuals were consistently least
healthy.6 We have previously
demonstrated our commitment to
advancing health equity and reducing
health disparities. In the past, and in
our ongoing efforts, we have strived to
identify and implement policies,
procedures, reporting protocols, and
other initiatives in a number of our
programs that address the impact of
SDOH on an individual’s health.
For the IPF Quality Reporting
Program, as discussed in section VI.D
below of this final rule, we are adopting
5 https://health.gov/healthypeople/priority-areas/
social-determinants-health.
6 Paula A. Braveman, Catherine Cubbin, Susan
Egerter, David R. Williams, and Elsie Pamuk, 2010:
Socioeconomic Disparities in Health in the
United States: What the Patterns Tell Us American
Journal of Public Health 100, S186_S196, https://
doi.org/10.2105/AJPH.2009.166082.
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the Facility Commitment to Health
Equity measure for the FY 2026
payment determination and subsequent
years, the Screening for Social Drivers of
Health measure beginning with
voluntary reporting of data reflecting
care provided in 2024 beginning in CY
2025 with required reporting for the FY
2027 payment determination and
subsequent years, and the Screen
Positive Rate for Social Drivers of
Health measure beginning with
voluntary reporting of data beginning in
CY 2024 with required reporting for the
FY 2027 payment determination and
subsequent years.
Additionally, in the technical report 7
accompanying the FY 2023 IPF PPS
proposed rule, we explained that we
analyzed the costs associated with
SDOH but found that our analysis was
confounded by a low frequency of IPF
claims reporting the applicable ICD–10
diagnosis codes. In response to the FY
2023 IPF PPS proposed rule we received
10 comments pertaining to the report on
the analysis of patient-level and facilitylevel adjustment factors, and areas of
interest for further research, including
additional SDOH analysis.
Working in collaboration with a
contractor, subsequent analysis has
shown that other SDOH codes, such as
Z59.9 Problem related to housing and
economic circumstances, unspecified,
are associated with statistically
significant, higher costs. In general, our
analysis found that claims that included
SDOH codes had lower costs than
claims that did not include such codes.
This finding is counterintuitive;
however, we note that studies have
found that there are disparities in the
reporting of SDOH codes, such as
homelessness.8 Additionally, our
analysis found that certain codes were
associated with increased cost for IPF
treatment. Specifically, the below SDOH
codes in the analysis were found to be
statistically significant and had a stay
count of greater than 100. These codes
had an adjustment factor above 1,
suggesting that these conditions may
increase relative costliness of IPF stays:
• Z559 Problems related to education
and literacy, unspecified.
• Z599 Problems related to housing
and economic circumstances,
unspecified.
• Z600 Problems of adjustment to
life-cycle transitions.
• Z634 Disappearance and death of
family member.
7 https://www.cms.gov/files/document/technicalreport-medicare-program-inpatient-psychiatricfacilities-prospective-payment-system.pdf.
8 https://aspe.hhs.gov/reports/health-conditionsamong-individuals-history-homelessness-researchbrief-0.
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• Z653 Problems related to other legal
circumstances.
• Z659 Problems related to
unspecified psychosocial
circumstances.
We solicited comments on these
findings and information about whether
it would be appropriate to consider
incorporating these codes into the IPF
PPS in the future, for example as a
patient-level adjustment. Specifically,
for codes that are ‘‘unspecified,’’ we
sought information about what types of
conditions or circumstances these codes
might represent. We sought any
information that commenters could
provide about the reasons for including
these codes on claims. We also
requested information on what factors
commenters believe we should consider
in order to better understand the cost
regression results presented above.
D. Public Comments Received in
Response to CY 2024 IPF PPS Proposed
Rule
We received 15 comments in response
to the FY 2024 IPF PPS proposed rule
pertaining to existing and future data
collection to inform revisions to the IPF
PPS as required by the CAA, 2023.
Commenters offered various suggestions
of patient characteristics and factors we
could consider for analysis.
Commenters included MedPAC, statelevel and national provider and patient
advocacy organizations, and health
systems.
We thank commenters for their
detailed responses to this comment
solicitation. We will take these
comments into consideration to
potentially inform future rulemaking.
VI. Inpatient Psychiatric Facility
Quality Reporting (IPFQR) Program
A. Background and Statutory Authority
The Inpatient Psychiatric Facility
Quality Reporting (IPFQR) Program is
authorized by section 1886(s)(4) of the
Act, and it applies to psychiatric
hospitals and psychiatric units paid by
Medicare under the IPF PPS (see section
VI.B. of this final rule). Section
1886(s)(4)(A)(i) of the Act requires the
Secretary to reduce by 2 percentage
points the annual update to the standard
federal rate for discharges for the IPF
occurring during such fiscal year 9 for
9 We note that the statute uses the term ‘‘rate
year’’ (RY). However, beginning with the annual
update of the inpatient psychiatric facility
prospective payment system (IPF PPS) that took
effect on July 1, 2011 (RY 2012), we aligned the IPF
PPS update with the annual update of the ICD
codes, effective on October 1 of each year. This
change allowed for annual payment updates and
the ICD coding update to occur on the same
schedule and appear in the same Federal Register
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any IPF that does not comply with
quality data submission requirements
under the IPFQR Program, set forth in
accordance with section 1886(s)(4)(C) of
the Act, with respect to an applicable
fiscal year.
Section 1886(s)(4)(C) of the Act
requires IPFs to submit to the Secretary
data on quality measures specified by
the Secretary under section
1886(s)(4)(D) of the Act. Except as
provided in section 1886(s)(4)(D)(ii) of
the Act, section 1886(s)(4)(D)(i) of the
Act requires that any measure specified
by the Secretary must have been
endorsed by the consensus-based entity
(CBE) with a contract under section
1890(a) of the Act. Section
1886(s)(4)(D)(ii) of the Act provides that,
in the case of a specified area or medical
topic determined appropriate by the
Secretary for which a feasible and
practical measure has not been endorsed
by the CBE with a contract under
section 1890(a) of the Act, the Secretary
may specify a measure that is not
endorsed as long as due consideration is
given to measures that have been
endorsed or adopted by a consensus
organization identified by the Secretary.
We refer readers to the FY 2019 IPF
PPS final rule (83 FR 38589) for a more
detailed discussion of the background
and statutory authority of the IPFQR
Program.
For the IPFQR Program, we refer to
the year in which an IPF would receive
the 2-percentage point reduction to the
annual update to the standard federal
rate as the payment determination year.
An IPF generally meets IPFQR Program
requirements by submitting data on
specified quality measures in a specified
time and manner during a data
submission period that occurs prior to
the payment determination year. These
data reflect a period prior to the data
submission period during which the IPF
furnished care to patients; this period is
known as the performance period. For
example, for a measure affecting FY
2026 payment determination, for which
CY 2024 is the performance period and
for which data are required to be
submitted in CY 2025, if an IPF did not
submit the data for this measure as
document, promoting administrative efficiency. To
reflect the change to the annual payment rate
update cycle, we revised the regulations at 42 CFR
412.402 to specify that, beginning October 1, 2012,
the IPF PPS RY means the 12-month period from
October 1 through September 30, which we refer to
as a ‘‘fiscal year’’ (FY) (76 FR 26435). Therefore,
with respect to the IPFQR Program, the terms ‘‘rate
year,’’ as used in the statute, and ‘‘fiscal year’’ as
used in the regulation, both refer to the period from
October 1 through September 30. For more
information regarding this terminology change, we
refer readers to section III of the RY 2012 IPF PPS
final rule (76 FR 26434 through 26435).
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specified during CY 2025 (even if the
IPF meets all other IPFQR Program
requirements for the FY 2026 payment
determination) we would reduce by 2percentage points that IPF’s update for
the FY 2026 payment determination
year.
In the FY 2024 IPF PPS proposed rule
(88 FR 21273), we proposed to codify
the IPFQR Program requirements
governing IPF reporting on quality
measures in a new regulation at
§ 412.433, which is the section
preceding our existing regulation
governing reconsideration and appeals
procedures for IPFQR Program decisions
in our regulations at § 412.434.
Specifically, we proposed to codify a
general statement of the IPFQR Program
authority and structure at § 412.433(a).
Paragraph (a) will cite section 1886(s)(4)
of the Act, which requires the Secretary
to implement a quality reporting
program for inpatient psychiatric
hospitals and psychiatric units.
Paragraph (a) will also state that IPFs
paid under the IPF PPS as provided in
section 1886(s)(1) of the Act that do not
report data required for the quality
measures selected by the Secretary in a
form and manner, and at a time
specified by the Secretary will incur a
2.0 percentage point reduction to the
annual update to the standard federal
rate with respect to the applicable fiscal
year.
We solicited comments on this
proposal.
Comment: One commenter requested
clarification regarding whether there are
penalties for facilities that do not meet
all the reporting requirements for a
specific year.
Response: The IPFQR Program is a
pay-for-reporting program. IPFs are not,
and will not be, penalized based on
their performance on measures reported
to CMS as part of the IPFQR Program.
However, if an IPF does not comply
with quality data submission
requirements under the IPFQR Program
for a given fiscal year, section
1886(s)(4)(A)(i) of the Act requires the
Secretary to reduce by 2 percentage
points the annual update to the standard
federal rate for discharges for the IPF
occurring during such fiscal year.
We specifically proposed to codify
established IPFQR Program
requirements, particularly those set
forth in the statute at section 1886(s)(4)
of the Act and our prior rulemaking, in
a new regulation at § 412.433. Our
proposal to codify penalties for an IPF’s
failure to submit data as required by the
IPFQR Program at § 412.433(a) merely
reiterates the penalty already required
by the statute set forth at section
1886(s)(4) of the Act.
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Final Decision: After consideration of
the public comments we received, we
are finalizing codification of the IPFQR
Program requirements governing IPF
reporting on quality measures at a new
regulation at § 412.433. We are
finalizing the regulation text as
proposed except that we are correcting
one typographical error in which the
‘‘Act’’ was inadvertently referred to as
the ‘‘act.’’
B. Covered Entities
In the FY 2013 IPPS/LTCH PPS final
rule (77 FR 53645), we established that
the IPFQR Program’s quality reporting
requirements cover those psychiatric
hospitals and psychiatric units paid by
Medicare under IPF PPS in accordance
with § 412.404(b). Generally, psychiatric
hospitals and psychiatric units within
acute care and critical access hospitals
(CAHs) that treat Medicare patients are
paid under the IPF PPS. Consistent with
previous regulations, we continue to use
the terms ‘‘facility’’ or ‘‘IPF’’ to refer to
both inpatient psychiatric hospitals and
psychiatric units. This usage follows the
terminology in our IPF PPS regulations
at § 412.402. For more information on
covered entities, we refer readers to the
FY 2013 IPPS/LTCH PPS final rule (77
FR 53645).
C. Previously Finalized Measures
The current IPFQR Program includes
14 measures for the FY 2024 payment
determination. For more information on
these measures, we refer readers to
Table 20 of this final rule (see section
VI.G of this final rule).
D. Measure Adoption
We strive to put patients and
caregivers first, ensuring they are
empowered to partner with their
clinicians in their healthcare decisionmaking using information from datadriven insights that are increasingly
aligned with meaningful quality
measures. We support technology that
reduces burden and allows clinicians to
focus on providing high-quality
healthcare for their patients. We also
support innovative approaches to
improve quality, accessibility, and
affordability of care while paying
particular attention to improving
clinicians’ and beneficiaries’
experiences when interacting with our
programs. In combination with other
efforts across HHS, we believe the
IPFQR Program helps to incentivize
IPFs to improve healthcare quality and
value while giving patients and
providers the tools and information
needed to make the best individualized
decisions. Consistent with these goals,
our objective in selecting quality
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measures for the IPFQR Program is to
balance the need for information on the
full spectrum of care delivery and the
need to minimize the burden of data
collection and reporting. We have
primarily focused on measures that
evaluate critical processes of care that
have significant impact on patient
outcomes and support CMS and HHS
priorities for improved quality and
efficiency of care provided by IPFs.
When possible, we also propose to
incorporate measures that directly
evaluate patient outcomes and
experience.
We refer readers to the CMS National
Quality Strategy,10 the Behavioral
Health Strategy,11 the Framework for
Health Equity,12 and the Meaningful
Measures Framework 13 for information
related to our priorities in selecting
quality measures.
recommendations provided by this
multi-stakeholder group in selecting all
measures for the IPFQR Program.
Information about the multistakeholder group’s input on each of our
newly adopted measures is described in
the following subsections. In our
evaluation of the IPFQR Program
measure set, we identified four
measures that we believe are
appropriate for adoption for the IPFQR
Program:
• Facility Commitment to Health
Equity;
• Screening for Social Drivers of
Health;
• Screen Positive Rate for Social
Drivers of Health; and
• Psychiatric Inpatient Experience
(PIX) Survey.
These four measures are described in
the following subsections.
1. Measure Selection Process
Section 1890A of the Act requires that
the Secretary establish and follow a prerulemaking process, in coordination
with the consensus-based entity (CBE)
with a contract under section 1890 of
the Act, to solicit input from certain
groups regarding the selection of quality
and efficiency measures for the IPFQR
Program. Before being proposed for
inclusion in the IPFQR Program,
measures are placed on a list of
Measures Under Consideration (MUC)
list, which is published annually on
behalf of CMS by the consensus-based
entity (CBE),14 with which the Secretary
must contract as required by section
1890(a) of the Act. Following
publication on the MUC list, a multistakeholder group convened by the CBE
reviews the measures under
consideration for the IPFQR Program,
among other federal programs, and
provides input on those measures to the
Secretary. We consider the input and
2. Adoption of the Facility Commitment
to Health Equity Measure Beginning
With the CY 2024 Reporting Period
(Data Submitted in CY 2025)/FY 2026
Payment Determination
10 Schreiber, M, Richards, A, et al. (2022). The
CMS National Quality Strategy: A Person-Centered
Approach to Improving Quality. Available at:
https://www.cms.gov/blog/cms-national-qualitystrategy-person-centered-approach-improvingquality. Accessed on February 20, 2023.
11 CMS. (2022). CMS Behavioral Health Strategy.
Available at https://www.cms.gov/cms-behavioralhealth-strategy. Accessed on February 20, 2023.
12 CMS. (2022). CMS Framework for Health
Equity 2022–2032. Available at https://
www.cms.gov/files/document/cms-frameworkhealth-equity-2022.pdf. Accessed on February 20,
2023.
13 CMS. (2022). Meaningful Measures 2.0: Moving
from Measure Reduction to Modernization.
Available at https://www.cms.gov/medicare/
meaningful-measures-framework/meaningfulmeasures-20-moving-measure-reductionmodernization. Accessed on February 20, 2023.
14 In previous years, we referred to the consensusbased entity by corporate name. We have updated
this language to refer to the consensus-based entity
more generally.
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a. Background
Significant and persistent disparities
in healthcare outcomes exist in the
United States. For example, belonging to
a racial or ethnic minority group, living
with a disability, being a member of the
lesbian, gay, bisexual, transgender, and
queer (LGBTQ+) community, being a
member of a religious minority, living in
a rural area, or being near or below the
poverty level, is often associated with
worse health
outcomes.15 16 17 18 19 20 21 22 23 24
15 Joynt KE, Orav E, Jha AK. (2011). Thirty-Day
Readmission Rates for Medicare Beneficiaries by
Race and Site of Care. JAMA, 305(7), 675–681.
Available at: https://jamanetwork.com/journals/
jama/fullarticle/645647. Accessed on February 13,
2023.
16 Lindenauer PK, Lagu T, Rothberg MB, et al.
(2013). Income Inequality and Thirty-Day Outcomes
After Acute Myocardial Infarction, Heart Failure,
and Pneumonia: Retrospective Cohort Study. BMJ,
346. Available at: https://doi.org/10.1136/bmj.f521.
Accessed on February 13, 2023.
17 Trivedi AN, Nsa W, Hausmann LRM, et al.
(2014). Quality and Equity of Care in U.S. Hospitals.
N Engl J Med, 371(24), 2298–2308. Available at:
https://www.nejm.org/doi/10.1056/NEJMsa1405003.
Accessed on February 13, 2023.
18 Polyakova, M, Udalova V, et al. (2021). Racial
Disparities In Excess All-Cause Mortality During
The Early COVID–19 Pandemic Varied
Substantially Across States. Health Affairs, 40(2),
307–316. Available at: https://doi.org/10.1377/
hlthaff.2020.02142. Accessed on February 14, 2023.
19 Rural Health Research Gateway. (2018). Rural
Communities: Age, Income, and Health Status.
Rural Health Research Recap. Available at: https://
www.ruralhealthresearch.org/assets/2200–8536/
rural-communities-age-income-health-statusrecap.pdf. Accessed on February 14, 2023.
20 HHS Office of Minority Health. (2020). Progress
Report to Congress, 2020 Update on the Action Plan
to Reduce Racial and Ethnic Health Disparities.
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Numerous studies have shown that
among Medicare beneficiaries, racial
and ethnic minority individuals often
receive clinical care of lower quality,
report having worse care experiences,
and experience more frequent hospital
readmissions and procedural
complications.25 26 27 28 29 30 Readmission
rates in the Hospital Readmissions
Reduction Program have been shown to
be higher among Black and Hispanic
Medicare beneficiaries with common
Department of Health and Human Services.
Available at: https://www.minorityhealth.hhs.gov/
assets/PDF/Update_HHS_Disparities_DeptFY2020.pdf . Accessed on February 14, 2023.
21 Heslin KC, Hall JE. (2021). Sexual Orientation
Disparities in Risk Factors for Adverse COVID–19
Related Outcomes, by Race/Ethnicity—Behavioral
Risk Factor Surveillance System, United States,
2017–2019. MMWR Morb Mortal Wkly Rep, 70(5),
149. Available at: https://www.cdc.gov/mmwr/
volumes/70/wr/mm7005a1.htm. Accessed on
February 14, 2023.
22 Poteat TC, Reisner SL, Miller M, Wirtz AL.
(2020). COVID–19 Vulnerability of Transgender
Women With and Without HIV Infection in the
Eastern and Southern U.S. medRxiv. Available at:
https://www.medrxiv.org/content/10.1101/
2020.07.21.20159327v1.full.pdf. Accessed on
February 14, 2023.
23 Vu M, Azmat A, Radejko T, Padela AI. (2016).
Predictors of Delayed Healthcare Seeking Among
American Muslim Women. Journal of Women’s
Health, 25(6), 586–593. Available at: https://
www.ncbi.nlm.nih.gov/pmc/articles/PMC5912720/.
Accessed on February 14, 2023.
24 Nadimpalli SB, Cleland CM, Hutchinson MK,
Islam N, Barnes LL, Van Devanter N. (2016). The
Association Between Discrimination and the Health
of Sikh Asian Indians. Health Psychology, 35(4),
351–355. Available at: https://doi.org/10.1037/
hea0000268. Accessed o n February 14, 2023.
25 CMS Office of Minority Health. (2020). Racial,
Ethnic, and Gender Disparities in Healthcare in
Medicare Advantage. Baltimore, MD: Centers for
Medicare & Medicaid Services. Available at: https://
www.cms.gov/files/document/2020-national-levelresults-race-ethnicity-and-gender-pdf.pdf Accessed
on February 14, 2023.
26 CMS Office of Minority Health. (2018). Guide
to Reducing Disparities in Readmissions. Available
at: https://www.cms.gov/About-CMS/AgencyInformation/OMH/Downloads/OMH_
Readmissions_Guide.pdf. Accessed on February 14,
2023.
27 Singh JA, Lu X, et al. (2014). Racial Disparities
in Knee and Hip Total Joint Arthroplasty: An 18year analysis of national Medicare data. Ann
Rheum Dis., 73(12), 2107–15. Available at: https://
ard.bmj.com/content/73/12/2107.full. Accessed on
February 14, 2023.
28 Rivera-Hernandez M, Rahman M, Mor V,
Trivedi AN. (2019). Racial Disparities in
Readmission Rates among Patients Discharged to
Skilled Nursing Facilities. J Am Geriatr Soc., 67(8),
1672–1679. Available at: https://doi.org/10.1111/
jgs.15960. Accessed on February 14, 2023.
29 Joynt KE, Orav E, Jha AK. (2011). Thirty-Day
Readmission Rates for Medicare Beneficiaries by
Race and Site of Care. JAMA, 305(7), 675–681.
Available at: https://jamanetwork.com/journals/
jama/fullarticle/645647. Accessed on February 13,
2023.
30 Tsai TC, Orav EJ, Joynt KE. (2014). Disparities
in Surgical 30-day Readmission Rates for Medicare
Beneficiaries by Race and Site of Care. Ann Surg.,
259(6), 1086–1090. Available at: https://
www.ncbi.nlm.nih.gov/pmc/articles/PMC4107654/.
Accessed on February 14, 2023.
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conditions, including congestive heart
failure and acute myocardial infarction.
31 32 33 34 35 Data indicate that, even after
accounting for factors such as
socioeconomic conditions, members of
racial and ethnic minority groups
reported experiencing lower quality of
healthcare.36 Evidence of differences in
quality of care received among people
from racial and ethnic minority groups
shows worse health outcomes,
including a higher incidence of diabetes
complications such as retinopathy.37
Additionally, inequities in the social
drivers of health (SDOH) affecting these
groups, such as poverty and healthcare
access, are interrelated and influence a
wide range of health and quality-of-life
outcomes and risks.38
Because we are working toward the
goal of all patients receiving highquality healthcare, regardless of
individual characteristics, we are
committed to supporting healthcare
organizations in building a culture of
31 Rodriguez F, Joynt KE, Lopez L, Saldana F, Jha
AK. (2011). Readmission Rates for Hispanic
Medicare Beneficiaries with Heart Failure and
Acute Myocardial Infarction. Am Heart J., 162(2),
254–261 e253. Available at: https://
www.sciencedirect.com/science/article/pii/
S0002870311003966?viewFullText=true. Accessed
on February 14, 2023.
32 Centers for Medicare & Medicaid Services.
(2014). Medicare Hospital Quality Chartbook:
Performance Report on Outcome Measures.
Available at: https://www.hhs.gov/guidance/sites/
default/files/hhs-guidance-documents/YNH_
Chartbook_2014_508Compliant_FINAL.pdf.
Accessed on February 14, 2023.
33 CMS Office of Minority Health. (2018). Guide
to Reducing Disparities in Readmissions. Available
at: https://www.cms.gov/About-CMS/AgencyInformation/OMH/Downloads/OMH_
Readmissions_Guide.pdf. Accessed on February 14,
2023.
34 Prieto-Centurion V, Gussin HA, Rolle AJ,
Krishnan JA. (2013). Chronic Obstructive
Pulmonary Disease Readmissions at Minority
Serving Institutions. Ann Am Thorac Soc., 10(6),
680–684. Available at: https://doi.org/10.1513/
AnnalsATS.201307-223OT. Accessed on February
14, 2023.
35 Joynt KE, Orav E, Jha AK. (2011). Thirty-Day
Readmission Rates for Medicare Beneficiaries by
Race and Site of Care. JAMA, 305(7), 675–681.
Available at: https://jamanetwork.com/journals/
jama/fullarticle/645647. Accessed on February 13,
2023.
36 Nelson AR. (2003). Unequal Treatment: Report
of the Institute of Medicine on Racial and Ethnic
Disparities in Healthcare. The Annals of Thoracic
Surgery, 76(4), S1377–S1381. https://
www.annalsthoracicsurgery.org/action/
showPdf?pii=S0003-4975%2803%2901205-0.
Accessed on February 14, 2023.
37 Peek, ME, Odoms-Young, A, et al. (2010). Race
and Shared Decision-Making: Perspectives of
African-Americans with diabetes. Social Science &
Medicine, 71(1), 1–9. Available at: https://
www.ncbi.nlm.nih.gov/pmc/articles/PMC2885527/.
Accessed on February 14, 2023.
38 Department of Health and Human Services.
(2023). Healthy People 2030: Social Determinants of
Health. Available at: https://health.gov/
healthypeople/priority-areas/social-determinantshealth. Accessed on February 20, 2023.
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safety and equity that focuses on
educating and empowering their
workforce to recognize and eliminate
health disparities. This includes
patients receiving the right care, at the
right time, in the right setting for their
condition(s), regardless of those
characteristics.
In the FY 2022 IPF PPS final rule (86
FR 42625 through 42632), we
summarized the comments we received
in response to our Request for
Information (RFI) on closing health
equity gaps in our quality programs,
specifically the IPFQR Program. In
response to this RFI, several
commenters recommended that we
consider a measure of organizational
commitment to health equity. These
commenters further described how
infrastructure supports delivery of
equitable care. In the FY 2023 IPF PPS
final rule (87 FR 46865 through 46873),
we described our RFI on overarching
principles for measuring equity and
healthcare quality across our quality
programs and summarized the
comments we received in response to
that RFI. Because we had specifically
solicited comments on the potential for
a structural measure assessing an IPF’s
commitment to health equity, many
commenters provided input on a
structural measure. While many
commenters supported the concept, one
commenter expressed concern with this
measure concept and stated that there is
no evidence that performance on this
measure will lead to improved patient
outcomes (87 FR 46872 through 46873).
However, we believe that strong and
committed leadership from IPF
executives and board members is
essential and can play a role in shifting
organizational culture and advancing
equity goals.
Additionally, studies demonstrate
that facility leadership can positively
influence culture for better quality,
patient outcomes, and experience of
care.39 40 41 A systematic review of 122
39 Bradley EH, Brewster AL, et al. (2018). How
Guiding Coalitions Promote Positive Culture
Change in Hospitals: A Longitudinal Mixed
Methods Interventional Study. BMJ Qual Saf., 27(3),
218–225. Available at: https://
qualitysafety.bmj.com/content/qhc/27/3/
218.full.pdf. Accessed on February 14, 2023.
40 Smith SA, Yount N, Sorra J. (2017). Exploring
Relationships Between Hospital Patient Safety
Culture and Consumer Reports Safety Scores. BMC
Health Services Research, 17(1), 143. Available at:
https://bmchealthservres.biomedcentral.com/
articles/10.1186/s12913-017-2078-6. Accessed on
February 14, 2023.
41 Keroack MA, Youngberg BJ, et al. (2007).
Organizational Factors Associated with High
Performance in Quality and Safety in Academic
Medical Centers. Acad Med., 82(12), 1178–86.
Available at: https://journals.lww.com/
academicmedicine/Fulltext/2007/12000/
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published studies showed that strong
leadership that prioritized safety,
quality, and the setting of clear guidance
with measurable goals for improvement
resulted in high-performing facilities
with better patient outcomes.42
Therefore, we believe leadership
commitment to health equity will have
a parallel effect in contributing to a
reduction in health disparities.
Further, we note that the Agency for
Healthcare Research and Quality
(AHRQ) and The Joint Commission
(TJC) identified that facility leadership
plays an important role in promoting a
culture of quality and safety.43 44 45 For
instance, AHRQ research shows that a
facility’s board can influence quality
and safety in a variety of ways, not only
through strategic initiatives, but also
through more direct interactions with
frontline workers.46
In addition, the Institute of Healthcare
Improvement’s (IHI’s) research of 23
health systems throughout the United
States and Canada shows that health
equity must be a priority championed
by leadership teams to improve both
patient access to needed healthcare
services and outcomes among
populations that have been
disadvantaged by the healthcare
system.47 This IHI study specifically
identified concrete actions to make
advancing health equity a core strategy,
Organizational_Factors_Associated_with_
High.14.aspx. Accessed on February 14, 2023.
42 Millar R, Mannion R, Freeman T, et al. (2013).
Hospital Board Oversight of Quality and Patient
Safety: A Narrative Review and Synthesis of Recent
Empirical Research. The Milbank Quarterly, 91(4),
738–70. Available at: https://
onlinelibrary.wiley.com/doi/10.1111/14680009.12032. Accessed February 14, 2023.
43 Agency for Healthcare Research and Quality.
Leadership Role in Improving Patient Safety.
Patient Safety Primer, September 2019. Available at:
https://psnet.ahrq.gov/primer/leadership-roleimproving-safety. Accessed on February 14, 2023.
44 Joint Commission on Accreditation of
Healthcare Organizations, USA. The essential role
of leadership in developing a safety culture.
Sentinel Event Alert. 2017 (Revised June 2021).
Available at: https://www.jointcommission.org/-/
media/tjc/documents/resources/patient-safetytopics/sentinel-event/sea-57-safety-culture-andleadership-final2.pdf. Accessed on February 15,
2023.
45 See information on launch of new ‘‘Health Care
Equity Certification’’ in July 2023 from Joint
Commission on Accreditation of Healthcare
Organizations, USA, available at: https://
www.jointcommission.org/our-priorities/healthcare-equity/health-care-equity-prepublication/.
Accessed on February 15, 2023.
46 Agency for Healthcare Research and Quality.
Leadership Role in Improving Patient Safety.
Patient Safety Primer. (2019). Available at: https://
psnet.ahrq.gov/primer/leadership-role-improvingsafety. Accessed on February 14, 2023.
47 Mate KS and Wyatt R. (2017). Health Equity
Must Be a Strategic Priority. NEJM Catalyst.
Available at: https://catalyst.nejm.org/doi/full/
10.1056/CAT.17.0556. Accessed on February 15,
2023.
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including establishing this goal as a
leader-driven priority alongside
organizational development structures
and processes.48
Based upon these findings, we believe
that IPF leadership can be instrumental
in setting specific, measurable,
attainable, realistic, and time-based
(SMART) goals to assess progress
towards achieving equity goals and
ensuring high-quality care is accessible
to all. Therefore, consistent with the
Hospital Inpatient Quality Reporting
(IQR) Program’s adoption of an
attestation-based structural measure in
the FY 2023 IPPS/LTCH PPS final rule
(87 FR 49191 through 49201), we
proposed to adopt an attestation-based
structural measure, Facility
Commitment to Health Equity, to
address health equity beginning with
the CY 2024 reporting period/FY 2026
payment determination.
The first pillar of our strategic
priorities 49 reflects our deep
commitment to improvements in health
equity by addressing the health
disparities that underly our health
system. In line with this strategic pillar,
we developed this structural measure to
assess facility commitment to health
equity across five domains (described in
Table 17 in section VI.D.2.b of this final
rule) using a suite of organizational
competencies aimed at achieving health
equity for racial and ethnic minority
groups, people with disabilities,
members of the LGBTQ+ community,
individuals with limited English
proficiency, rural populations, religious
minorities, and people facing
socioeconomic challenges. We believe
these elements are actionable focus
areas, and assessment of IPFs’
leadership commitment to them is
foundational.
We also believe adoption of the
Facility Commitment to Health Equity
measure will incentivize IPFs to collect
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48 Mate KS and Wyatt R. (2017). Health Equity
Must Be a Strategic Priority. NEJM Catalyst.
Available at: https://catalyst.nejm.org/doi/full/
10.1056/CAT.17.0556. Accessed on February 15,
2023.
49 Brooks-LaSure, C. (2021). My First 100 Days
and Where We Go From Here: A Strategic Vision
for CMS. Centers for Medicare & Medicaid.
Available at: https://www.cms.gov/blog/my-first100-days-and-where-we-go-here-strategic-visioncms. Accessed on February 15, 2023. Also see
https://www.cms.gov/cms-strategic-plan.
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and utilize data to identify critical
equity gaps, implement plans to address
these gaps, and ensure that resources are
dedicated toward addressing health
equity initiatives. While many factors
contribute to health equity, we believe
this measure is an important step
toward assessing IPFs’ leadership
commitment, and a fundamental step
toward closing the gap in equitable care
for all populations. We note that this
measure is not intended to encourage
IPFs to act on any one data element or
domain, but instead encourages IPFs to
analyze their own findings to
understand if there are any demographic
factors (for example, race, national
origin, primary language, and ethnicity)
as well as SDOHs (for example, housing
status and food security) associated with
underlying inequities and, in turn,
develop solutions to deliver more
equitable care. Thus, the Facility
Commitment to Health Equity measure
aims to support IPFs in leveraging
available data, pursuing focused quality
improvement activities, and promoting
efficient and effective use of resources.
The Facility Commitment to Health
Equity measure aligns with the measure
previously adopted in the Hospital IQR
Program, and we refer readers to the FY
2023 IPPS/LTCH PPS final rule (87 FR
49191 through 49201) for more
information regarding the measure’s
adoption in the Hospital IQR Program.
The five domains of the Facility
Commitment to Health Equity measure
are adapted from the CMS Office of
Minority Health’s Building an
Organizational Response to Health
Disparities framework, which focuses
on data collection, data analysis, culture
of equity, and quality improvement.50
The Facility Commitment to Health
Equity measure also aligns with our
efforts under the Meaningful Measures
Framework, which identifies highpriority areas for quality measurement
and improvement to assess core issues
most critical to high-quality healthcare
and improving patient outcomes.51 In
50 CMS. (2021). Building an Organizational
Response to Health Disparities [Fact Sheet].
Available at: https://www.cms.gov/About-CMS/
Agency-Information/OMH/Downloads/HealthDisparities-Guide.pdf. Accessed on February 15,
2023.
51 Centers for Medicare & Medicaid Services.
Meaningful Measures Framework. Available at:
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2021, we launched Meaningful
Measures 2.0 to promote innovation and
modernization of all aspects of quality,
and to address a wide variety of settings,
stakeholders, and measure
requirements.52 We are addressing
healthcare priorities and gaps with
Meaningful Measures 2.0 by leveraging
quality measures to promote equity and
close gaps in care. The Facility
Commitment to Health Equity measure
supports these efforts and is aligned
with the Meaningful Measures Area of
‘‘Equity of Care’’ and the Meaningful
Measures 2.0 goal to ‘‘Leverage Quality
Measures to Promote Equity and Close
Gaps in Care.’’ This measure also
supports the Meaningful Measures 2.0
objective to commit to a patientcentered approach in quality measure
and value-based incentives programs to
ensure that quality and safety measures
address health equity.
b. Overview of Measure
The Facility Commitment to Health
Equity measure will assess IPFs’
commitment to health equity using a
suite of equity-focused organizational
competencies aimed at achieving health
equity for populations that have been
disadvantaged, marginalized, and
underserved by the healthcare system.
As previously noted, these populations
include, but are not limited to, racial
and ethnic minority groups, people with
disabilities, members of the LGBTQ+
community, individuals with limited
English proficiency, rural populations,
religious minorities, and people facing
socioeconomic challenges. Table 17 sets
forth the five attestation domains, and
the elements within each of those
domains, to which an IPF will
affirmatively attest for the IPF to receive
credit for that domain within the
Facility Commitment to Health Equity
measure.
https://www.cms.gov/Medicare/Quality-InitiativesPatient-Assessment-Instruments/
QualityInitiativesGenInfo/CMS-Quality-Strategy.
Accessed on February 15, 2023.
52 CMS. (2022). Meaningful Measures 2.0: Moving
from Measure Reduction to Modernization.
Available at https://www.cms.gov/medicare/
meaningful-measures-framework/meaningfulmeasures-20-moving-measure-reductionmodernization. Accessed on February 20, 2023.
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(1) Measure Calculation
The Facility Commitment to Health
Equity measure consists of five
attestation-based questions, each
representing a separate domain of the
IPF’s commitment to addressing health
equity. Some of these domains have
multiple elements to which an IPF will
be required to attest. For an IPF to
affirmatively attest ‘‘yes’’ to a domain,
and receive credit for that domain, the
IPF would evaluate and determine
whether it engages in each of the
elements that comprise that domain.
Each of the domains will be represented
in the denominator as a point, for a total
of five points (that is, one point per
domain).
The numerator of the Facility
Commitment to Health Equity measure
will capture the total number of domain
attestations that the IPF is able to affirm.
An IPF that affirmatively attests to each
element within the five domains will
receive the maximum five points.
An IPF will only receive a point for
a domain if it attests ‘‘yes’’ to all related
elements within that domain. There is
no ‘‘partial credit’’ for elements. For
example, for Domain 1 (‘‘Facility
commitment to reducing healthcare
disparities is strengthened when equity
is a key organizational priority’’), an IPF
will evaluate and determine whether its
strategic plan meets each of the
elements described in (A) through (D)
(see Table 17 in section VI.D.2.b of this
final rule). If the IPF’s strategic plan
meets all four of these elements, the IPF
would affirmatively attest ‘‘yes’’ to
Domain 1 and would receive one (1)
point for that attestation. An IPF will
not be able to receive partial credit for
a domain. For example, if the IPF’s
strategic plan meets elements (A) and
(B), but not (C) and (D), of Domain 1,
then the IPF would not be able to
affirmatively attest ‘‘yes’’ to Domain 1
and would not receive a point for that
attestation, and instead would receive
zero points for Domain 1.
In response to our RFI on the
potential for a structural measure
assessing an IPF’s commitment to health
equity, several commenters expressed
concern that such a measure would be
difficult for IPFs to report because of the
requirement to use certified electronic
health record (EHR) technology for
Domain 2 (87 FR 46972 through 46873).
We believe that use of certified EHR
technology is an important element of
collecting valid and reliable
demographic and social drivers of
health data on patients served in an IPF
and that use of this technology
facilitates data analytics to ensure
consistent, high-quality, equitable care.
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However, we recognize that some IPFs
may face challenges to adopting
certified EHR technology. We note that
the IPFQR Program is a pay-forreporting program, not a pay-forperformance program, and therefore
IPFs that do not have certified EHR
technology can attest that they satisfy
the other domains, as applicable, and
receive a score of 0–4 out of 5 without
any penalties.
(2) Review by the Measure Applications
Partnership (MAP) 53
We included the Facility Commitment
to Health Equity measure on the
publicly available MUC List, a list of
measures under consideration for use in
various Medicare programs.54 The
specifications for the Facility
Commitment to Health Equity measure,
which were available during the review
of the MUC List, are available on the
CMS website at: https://
mmshub.cms.gov/sites/default/files/
map-hospital-measure-specificationsmanual-2022.pdf.
The CBE-convened MAP Health
Equity Advisory Group reviewed the
MUC List and the Facility Commitment
to Health Equity measure (MUC 2022–
027) in detail on December 6 through 7,
2022.55 The MAP Health Equity
Advisory Group raised concerns that
this measure does not evaluate
outcomes and may not directly address
health inequities at a systemic level, but
generally agreed that a structural
measure such as this one represents
progress toward improving equitable
care.56
In addition, on December 8 through 9,
2022, the MAP Rural Health Advisory
Group reviewed the 2022 MUC List and
expressed support for this measure as a
step towards advancing access to and
quality of care with the caveat that
resource challenges exist in rural
communities.57
53 Interested parties convened by the consensusbased entity provide input and recommendations
on the Measures under Consideration (MUC) list as
part of the pre-rulemaking process required by
section 1890A of the Act. We refer readers to
https://p4qm.org/PRMR-MSR for more information.
54 Centers for Medicare & Medicaid Services. List
of Measures Under Consideration for December 1,
2022. Available at: https://mmshub.cms.gov/
measure-lifecycle/measure-implementation/prerulemaking/lists-and-reports.
55 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
56 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
57 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
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The MAP Hospital Workgroup
reviewed the 2022 MUC List on
December 13 through 14, 2022.58 The
MAP Hospital Workgroup recognized
that reducing health care disparities
would represent a substantial benefit to
overall quality of care but expressed
reservations about the measure’s link to
clinical outcomes. As stated in the MAP
recommendations document, the MAP
Hospital Workgroup members voted to
conditionally support the Facility
Commitment to Health Equity measure
for rulemaking pending: (1)
endorsement by the CBE; (2)
commitment to consideration of equity
related outcome measures in the future;
(3) provision of more clarity on the
Facility Commitment to Health Equity
measure and supplementing
interpretation with results; and (4)
verification of accurate attestation by
IPFs.59 Thereafter, the MAP
Coordinating Committee deliberated on
January 24 through 25, 2023 and
ultimately voted to uphold the MAP
Hospital Workgroup’s recommendation
to conditionally support the measure for
rulemaking.60
We believe that the Facility
Commitment to Health Equity measure
establishes an important foundation for
prioritizing the achievement of health
equity among IPFs participating in the
IPFQR Program. Our approach to
developing health equity measures has
been incremental to date, but we see
inclusion of such measures in the
IPFQR Program as informing efforts to
advance and achieve health equity not
only among IPFs, but also other acute
care settings. We believe this measure to
be a building block that lays the
groundwork for a future meaningful
suite of measures that would assess IPF
progress in providing high-quality
healthcare for all patients regardless of
social risk factors or demographic
characteristics.
(3) CBE Endorsement
We have not submitted this measure
for CBE endorsement at this time.
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
58 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
59 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
60 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
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Although section 1886(s)(4)(D)(i) of the
Act generally requires that measures
specified by the Secretary must be
endorsed by the entity with a contract
under section 1890(a) of the Act, section
1886(s)(4)(D)(ii) of the Act states that, in
the case of a specified area or medical
topic determined appropriate by the
Secretary for which a feasible and
practical measure has not been endorsed
by the entity with a contract under
section 1890(a) of the Act, the Secretary
may specify a measure that is not so
endorsed as long as due consideration is
given to measures that have been
endorsed or adopted by a consensus
organization identified by the Secretary.
We reviewed measures endorsed by
consensus organizations and were
unable to identify any other measures
on this topic endorsed by a consensus
organization, and therefore, we believe
the exception in section 1886(s)(4)(D)(ii)
of the Act applies.
c. Data Collection, Submission, and
Reporting
IPFs are required to submit
information for structural measures
once annually using a CMS-approved
web-based data collection tool available
within the Hospital Quality Reporting
(HQR) System. For more information
about our previously finalized policies
related to reporting of structural
measures, we refer readers to the FY
2014 IPPS/LTCH PPS final rule (78 FR
50890 through 50901) and the FY 2015
IPF PPS final rule (79 FR 45963 through
45964 and 45976). Given the role of
committed leadership in improving
health outcomes for all patients, we
proposed to adopt this measure
beginning with attestations submitted to
CMS in CY 2025 reflecting the CY 2024
reporting period and affecting the FY
2026 payment determination.
We invited comments on our
proposed adoption of the Facility
Commitment to Health Equity Measure
beginning with the FY 2026 payment
determination.
Comment: Many commenters
supported adoption of the Facility
Commitment to Health Equity measure.
One commenter stated that alignment
with other programs will support
consistent measurement across the
continuum of patient care. Several
commenters stated that facilities’
commitment to health equity is
particularly important for IPFs because
of health disparities experienced by
patients with mental health conditions.
Several commenters stated that the
Facility Commitment to Health Equity
measure is consistent with new
standards from The Joint Commission.
One commenter stated that facilities
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attesting to their commitment to health
equity will help empower the healthcare
workforce to recognize and eliminate
health disparities.
Response: We thank commenters for
their support of our proposal to adopt
the Facility Commitment to Health
Equity measure and agree that this
measure addresses a topic that is
important for IPF patients and this
setting.
Comment: Other commenters
recommended additional testing,
specifically in the IPF setting, to ensure
that this measure addresses unique
challenges associated with treating the
psychiatric patient population prior to
adoption of this measure. Some of these
commenters also recommended
engaging IPFs to voluntarily test the
measure to ensure usability,
acceptability, and face validity are met
for this setting.
Response: We acknowledge that this
measure was initially developed for the
general acute care setting. While we
recognize the value of measures
undergoing testing and evaluation of
validity and feasibility in the setting for
which they are being adopted, given the
urgency of achieving health equity and,
as there are currently no other existing
measures that address facility
commitment to health equity, we
believe it is important to implement this
measure as soon as feasible. Strong and
consistent facility leadership can be
instrumental in establishing specific,
measurable, and attainable goals to
advance equity priorities and improve
care for all patients in any care setting,
including patients who receive care in
inpatient psychiatric facilities. We
believe that this measure is equally
applicable to freestanding IPFs and
psychiatric units within acute care
facilities as it is to general acute care
settings. Leaders of health services
organizations across the health care
system, including both IPFs and acute
care hospitals, are likely to encounter
the same challenges and use the same
types of strategies to achieve
organizational goals related to
improving health equity within their
respective organizations. We note that
health equity is a critical topic for
patients treated in IPFs and that there
are high levels of health disparities
experienced by this patient population.
CMS will monitor measure
implementation and data reporting as
part of standard program and measure
review and will consider updates to the
measure if improvements are identified
through this process.
Comment: Many commenters
expressed concern that this measure has
not received endorsement by the CBE.
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51105
Response: While we recognize the
value of measures undergoing review for
potential CBE endorsement, given the
urgency of achieving health equity, we
believe it is important to implement this
measure beginning with the CY 2024
reporting period. We note that, in
accordance with section 1886(s)(4)(D)(ii)
of the Act, the Secretary may specify a
measure that is not so endorsed as long
as due consideration is given to
measures that have been endorsed or
adopted by a consensus organization
identified by the Secretary. We
reviewed measures endorsed by
consensus organizations and were
unable to identify any other measures
on this topic endorsed by a consensus
organization, and therefore, we believe
the exception in section 1886(s)(4)(D)(ii)
of the Act applies.
Comment: Some commenters
recommended that CMS defer adoption
of this measure until CMS and IPFs
have reviewed the Hospital IQR
Program’s implementation of this
measure to identify potential
improvements to data collection
processes that would reduce burden for
IPFs. These commenters stated that IPFs
often have fewer resources available for
data collection relative to acute care
hospitals.
Response: We acknowledge
commenters’ desire to be able to learn
from the experiences of acute care
hospitals reporting this measure. We
note that hospitals participating in the
Hospital IQR Program will have already
reported data on the similar Hospital
Commitment to Health Equity measure
for the FY 2025 payment determination
(that is, data submitted in CY 2024
representing the CY 2023 performance
period) (87 FR 49201) before the
reporting of the Facility Commitment to
Health Equity Measure for the IPFQR
Program begins with the FY 2026
payment determination. Given the
timing of this similar measure in the
Hospital IQR Program, we believe IPFs
will have had the opportunity to learn
from the experiences of acute care
hospitals, including best practices for
minimally burdensome assessment of
performance on the required domains.
Comment: Many commenters
supported adoption of this measure on
the condition that CMS commit to
development and adoption of health
equity related outcome measures in the
future.
Response: We believe this measure to
be a building block that lays the
groundwork for a more comprehensive
suite of measures that would assess
progress in providing high-quality
healthcare for all patients regardless of
social risk factors or demographic
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characteristics. This more
comprehensive suite of measures could
eventually include health equity related
outcome measures.
Comment: Many commenters
recommended that CMS establish a
process to ensure that results are
publicly reported in a way that helps
patients interpret IPF scores on the
Facility Commitment to Health Equity
measure.
Response: We believe this measure
will provide insightful information to
healthcare providers and the public on
the number of IPFs currently
participating in health equity strategic
planning, collecting data, using these
data to identify equity gaps, establishing
key performance indicators, and
reviewing them with hospital senior
leaders. We intend to provide
educational materials as part of our
outreach and public reporting of this
measure to ensure understanding and
interpretation of publicly reported data.
Comment: Many commenters
recommended that prior to adoption of
the Facility Commitment to Health
Equity measure CMS identify a means to
verify accurate attestation of
commitment by IPFs.
Response: We understand
commenters’ concerns regarding the
accuracy of provider self-reported data.
While we do not have a specific means
to validate IPFs’ attestation to this
measure, we do require all IPFs
participating in the IPFQR Program to
complete the Data Accuracy and
Completeness Acknowledgement
(DACA) each year, which requires
attestation that all of the information
reported to CMS for the IPFQR Program
is accurate and complete. For more
information on the IPFQR Program’s
DACA requirements, we refer readers to
the FY 2013 IPPS/LTCH PPS final rule
(77 FR 53658).
Comment: Several commenters
recommended that CMS update the
measure specifications so that IPFs
without certified EHR technology are
able to positively attest to all domains.
These commenters expressed concern
that public reporting of measure results
for IPFs that do not positively attest to
all domains because they are without
access to certified EHR technology
could lead the public to misinterpret the
results as a lack of commitment to
health equity when it is actually a
resource limitation which, the
commenters believed, is due to a lack of
federal funding for EHR
implementation.
Response: We acknowledge that some
IPFs may face challenges to adopting
certified EHR technology. We note that
the IPFQR Program is a pay-for-
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reporting program, not a pay-forperformance program, and therefore
IPFs that do not have certified EHR
technology can attest that they satisfy
the other domains, as applicable, and
receive a score of 0–4 out of 5 without
any penalties. We understand the
commenters’ concern that the public
may misinterpret IPFs’ reported results
that are due to resource limitations as a
lack of commitment to health equity. To
reduce the likelihood of
misinterpretation, we intend to provide
educational materials as part of our
outreach and public reporting of this
measure to ensure understanding and
appropriate interpretation of publicly
reported data.
Comment: Some commenters
recommended respecifying the measure
so that IPFs are scored on a zero to
eleven scale (one point for each element
within a domain) as opposed to a zero
to five scale (one point for each
domain). Other commenters
recommended only requiring attestation
for 3 out of 5 domains. Some of these
commenters stated that some domains
are harder to achieve or have more
required elements for attestation than
others and expressed the belief that
reducing the number of required
domains would address this concern.
Response: We believe the five
domains of this measure are actionable
focus areas, and assessment of facility
leadership commitment to them is
foundational. We also believe this
measure will incentivize providers to
collect and utilize data to identify
critical equity gaps, implement plans to
address any identified gaps, and ensure
that resources are dedicated toward
addressing health equity initiatives. The
five questions of the proposed structural
measure are adapted from the CMS
Office of Minority Health’s Building an
Organizational Response to Health
Disparities framework, which focuses
on data collection, data analysis, culture
of equity, and quality improvement.61
We believe that accomplishing each
element within a domain is important
together with the other elements to help
hospitals identify, prioritize, and take
action on health disparities.
Additionally, as discussed previously,
we note that the IPFQR Program is a
pay-for-reporting program, and IPFs are
not scored based on their performance
on measures.
Comment: Several commenters
expressed concern that IPFs may not
61 Centers for Medicare & Medicaid Services.
(2021). Building an Organizational Response to
Health Disparities [Fact Sheet]. U.S. Department of
Health and Human Services. Available at: https://
www.cms.gov/About-CMS/Agency-Information/
OMH/Downloads/Health-Disparities-Guide.pdf.
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report the measure consistently, and one
commenter recommended that CMS
provide clarification of key terms (such
as ‘‘strategic plan’’) to mitigate the risk
of inconsistent reporting.
Response: We note that Attestation
Guidance for the similar measure
adopted in the Hospital IQR Program
(the Hospital Commitment to Health
Equity measure), includes definitions of
key terms including ‘‘strategic plan,’’
which we define as ‘‘a written plan to
address health equity that is shared
across the hospital’’ (or facility in the
case of IPFs).62 To help with consistent
implementation, we will develop a
similar Attestation Guidance document
for IPFs as part of providing educational
and training materials, and which will
be conveyed through routine
communication channels to IPFs,
vendors, and QIOs, including, but not
limited to, issuing memos, emails, and
notices on a CMS website.
Comment: One commenter did not
support adoption of the Facility
Commitment to Health Equity measure
and expressed their belief that there is
insufficient evidence that this measure
leads to improved patient outcomes.
Response: We believe this measure is
an important foundational measure for
improving health equity among those
that have been disadvantaged or
underserved by the healthcare system.
Furthermore, as discussed in section
VI.D.2.a of the proposed rule, there is
substantial research showing differences
in care and experiences among these
populations (88 FR 21274 through
21275). We also believe adoption of the
Facility Commitment to Health Equity
measure will incentivize IPFs to collect
and utilize data to identify critical
equity gaps, implement plans to address
these gaps, and ensure that resources are
dedicated toward addressing health
equity initiatives. This measure aims to
support IPFs in leveraging available
data, pursuing focused quality
improvement activities, and promoting
efficient and effective use of resources.
Through this measure, providers are
encouraged to analyze their own data to
understand the many factors, including
race, ethnicity, and various social
drivers of health, such as housing
stability and food security, in order to
deliver more equitable care. We believe
the delivery of more equitable care will,
in turn, improve patient outcomes.
62 Available at: https://qualitynet.cms.gov/files/
6481de126f7752001c37e34f?
filename=AttstGdnceHCHEMeas_v1.1.pdf.
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Federal Register / Vol. 88, No. 147 / Wednesday, August 2, 2023 / Rules and Regulations
Final Decision: After consideration of
the public comments we received, we
are finalizing adoption of the Facility
Commitment to Health Equity measure
as proposed.
3. Adoption of the Screening for Social
Drivers of Health Measure Beginning
With Voluntary Reporting of CY 2024
Data Followed by Mandatory Reporting
Beginning With CY 2025 Data/FY 2027
Payment Determination
ddrumheller on DSK120RN23PROD with RULES3
a. Background
Health-related social needs (HRSNs),
which we define as individual-level,
adverse social conditions that negatively
impact an individual person’s health or
healthcare, are significant risk factors
associated with worse health outcomes
as well as increased healthcare
utilization.63 We believe that
consistently pursuing identification of
HRSNs would have two significant
benefits. First, HRSNs
disproportionately impact people who
have historically been underserved by
the healthcare system,64 and screening
helps identify individuals who may
have HRSNs. Second, screening for
HRSNs could support ongoing IPF
quality improvement initiatives by
providing data with which to stratify
patient risk and organizational
performance. Further, we believe that
IPFs collecting patient-level HRSN data
through screening is essential for the
long-term in encouraging meaningful
collaboration between healthcare
providers and community-based
organizations and in implementing and
evaluating related innovations in health
and social care delivery.
Health disparities manifest primarily
as worse health outcomes in population
groups where access to care is
inequitable.65 66 67 68 69 Such differences
63 Centers for Medicare & Medicaid Services.
(2021). A Guide to Using the Accountable Health
Communities Health-Related Social Needs
Screening Tool: Promising Practices and Key
Insights. June 2021. Available at: https://
innovation.cms.gov/media/document/ahcmscreeningtool-companion. Accessed on February 20,
2023.
64 American Hospital Association. (2020). Health
Equity, Diversity & Inclusion Measures for
Hospitals and Health System Dashboards. December
2020. Available at: https://ifdhe.aha.org/system/
files/media/file/2020/12/ifdhe_inclusion_
dashboard.pdf. Accessed on February 20, 2023.
65 Seligman, H.K., & Berkowitz, S.A. (2019).
Aligning Programs and Policies to Support Food
Security and Public Health Goals in the United
States. Annual Review of Public Health, 40(1), 319–
337. Available at: https://www.ncbi.nlm.nih.gov/
pmc/articles/PMC6784838/. Accessed on February
20, 2023.
66 The Physicians Foundation. (2020). Survey of
America’s Patients, Part Three. Available at: https://
physiciansfoundation.org/wp-content/uploads/
2020/10/2020-Physicians-Foundation-SurveyPart3.pdf. Accessed on February 20, 2023.
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persist across geography and healthcare
settings irrespective of improvements in
quality of care over time.70 71 72
Assessment of HRSNs is an essential
mechanism for capturing the interaction
between social, community, and
environmental factors associated with
health status and health outcomes.73 74 75
Growing evidence demonstrates that
specific HRSNs are directly associated
with patient health outcomes as well as
healthcare utilization, costs, and
performance in quality-based payment
programs.76 77 While widespread interest
67 Office of the Assistant Secretary for Planning
and Evaluation (ASPE) (2020). Report to Congress:
Social Risk Factors and Performance Under
Medicare’s Value-Based Purchasing Program
(Second of Two Reports). Available at: https://
aspe.hhs.gov/pdf-report/second-impact-report-tocongress. Accessed on February 20, 2023.
68 Trivedi AN, Nsa W, Hausmann LRM, et al.
(2014). Quality and Equity of Care in U.S. Hospitals.
N Engl J Med, 371(24), 2298–2308. Available at:
https://www.nejm.org/doi/10.1056/NEJMsa1405003.
Accessed on February 13, 2023.
69 Billioux, A., Verlander, K., Anthony, S., &
Alley, D. (2017). Standardized Screening for Health
Related Social Needs in Clinical Settings: The
Accountable Health Communities Screening Tool.
NAM Perspectives, 7(5). Available at: https://
doi.org/10.31478/201705b. Accessed on February
20, 2023.
70 Office of the Assistant Secretary for Planning
and Evaluation (ASPE) (2020). Report to Congress:
Social Risk Factors and Performance Under
Medicare’s Value-Based Purchasing Program
(Second of Two Reports). Available at: https://
aspe.hhs.gov/pdf-report/second-impact-report-tocongress. Accessed on February 20, 2023.≤
71 Hill-Briggs, F. (2021). Social Determinants of
Health and Diabetes: A Scientific Review. Diabetes
Care. Available at: https://diabetesjournals.org/
care/article/44/1/258/33180/Social-Determinantsof-Health-and-Diabetes-A. Accessed on February
20, 2023.
72 Khullar, D., MD. (2020). Association Between
Patient Social Risk and Physician Performance
American academy of Family Physicians.
Addressing Social Determinants of Health in
Primary Care team-based approach for advancing
health equity. Available at: https://www.aafp.org/
dam/AAFP/documents/patient_care/everyone_
project/team-based-approach.pdf. Accessed on
February 20, 2023.
73 Institute of Medicine. (2014). Capturing Social
and Behavioral Domains and Measures in
Electronic Health Records: Phase 2. Washington,
DC: The National Academies Press. Available at:
https://doi.org/10.17226/18951. Accessed on
February 20, 2023.
74 Alley, D.E., C.N. Asomugha, P.H. Conway, and
D.M. Sanghavi. (2016). Accountable Health
Communities—Addressing Social Needs through
Medicare and Medicaid. The New England Journal
of Medicine 374(1):8–11. Available at: https://
doi.org/10.1056/NEJMp1512532. Accessed on
February 20, 2023.
75 Centers for Disease Control and Prevention.
CDC COVID–19 Response Health Equity Strategy:
Accelerating Progress Towards Reducing COVID–19
Disparities and Achieving Health Equity. July 2020.
Available at: https://www.cdc.gov/coronavirus/
2019-ncov/community/health-equity/cdcstrategy.html. Accessed on February 2, 2023.
76 Zhang Y, Li J, Yu J, Braun RT, Casalino LP
(2021). Social Determinants of Health and
Geographic Variation in Medicare per Beneficiary
Spending. JAMA Network Open.
2021;4(6):e2113212. https://jamanetwork.com/
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51107
in addressing HRSNs exists, action is
inconsistent.78
While social risk factors account for
50 to 70 percent of health outcomes, the
mechanisms by which this connection
emerges are complex and
multifaceted.79 80 81 82 The persistent
interactions among individuals’ HRSNs,
medical providers’ practices and
behaviors, and community resources
significantly impact healthcare access,
quality, and ultimately costs, as
described in the CMS Equity Plan for
Improving Quality in Medicare.83 84 In
their 2018 survey, to which more than
8,500 physicians responded, the
journals/jamanetworkopen/fullarticle/2780864.
Accessed on February 20, 2023.
77 Khullar, D., Schpero, W.L., Bond, A.M., Qian,
Y., & Casalino, L.P. (2020). Association Between
Patient Social Risk and Physician Performance
Scores in the First Year of the Merit-based Incentive
Payment System. JAMA, 324(10), 975–983. https://
doi.org/10.1001/jama.2020.13129. Accessed on
February 20, 2023.
78 TK Fraze, AL Brewster, VA Lewis, LB Beidler,
GF Murray, CH Colla. Prevalence of screening for
food insecurity, housing instability, utility needs,
transportation needs, and interpersonal violence by
US physician practices and hospitals. JAMA
Network Open 2019; https://jamanetwork.com/
journals/jamanetworkopen/fullarticle/10.1001/
jamanetworkopen.2019.11514. Accessed on
February 20, 2023.
79 Kaiser Family Foundation. (2021). Racial and
Ethnic Health Inequities and Medicare. Available
at: https://www.kff.org/medicare/report/racial-andethnic-health-inequities-and-medicare/. Accessed
February 20, 2023.
80 Khullar, D., MD. (2020). Association Between
Patient Social Risk and Physician Performance
American academy of Family Physicians.
Addressing Social Determinants of Health in
Primary Care team-based approach for advancing
health equity. Available at: https://www.aafp.org/
dam/AAFP/documents/patient_care/everyone_
project/team-based-approach.pdf. Accessed on
February 20, 2023.
81 Hammond, G., Johnston, K., Huang, K., Joynt
Maddox, K. (2020). Social Determinants of Health
Improve Predictive Accuracy of Clinical Risk
Models for Cardiovascular Hospitalization, Annual
Cost, and Death. Circulation: Cardiovascular
Quality and Outcomes, 13 (6) 290–299. Available at:
https://doi.org/10.1161/
CIRCOUTCOMES.120.006752. Accessed on
February 20, 2023.
82 The Physicians Foundation. (2021).
Viewpoints: Social Determinants of Health.
Available at: https://physiciansfoundation.org/wpcontent/uploads/2019/08/The-PhysiciansFoundation-SDOH-Viewpoints.pdf. Accessed on
February 20, 2023.
83 Centers for Medicare & Medicaid Services.
(2021). Paving the Way to Equity: A Progress
Report. Available at: https://www.cms.gov/files/
document/paving-way-equity-cms-omh-progressreport.pdf. Accessed on February 20, 2023.
84 Centers for Medicare & Medicaid Services
Office of Minority Health. (2021). The CMS Equity
Plan for Improving Quality in Medicare. 2015–2021.
Available at: https://www.cms.gov/About-CMS/
Agency-Information/OMH/OMH_Dwnld-CMS_
EquityPlanforMedicare_090615.pdf#:∼:text=The
%20Centers%20for%20Medicare%20%26
%20Medicaid%20Services%20%28CMS
%29,evidence%20base%2C%20identifying
%20opportunities%2C%20and
%20gathering%20stakeholder%20input. Accessed
on February 20, 2023.
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Federal Register / Vol. 88, No. 147 / Wednesday, August 2, 2023 / Rules and Regulations
Physicians Foundation found that
almost 90 percent of these physician
respondents reported their patients had
a serious health problem linked to
poverty or other social conditions.85
Additionally, associations among
disproportionate health risk,
hospitalization, and adverse health
outcomes have been highlighted and
magnified by the COVID–19
pandemic.86 87
In 2017, CMS’ Center for Medicare
and Medicaid Innovation (CMMI)
launched the Accountable Health
Communities (AHC) Model to test the
impact of systematically identifying and
addressing the HRSNs of Medicare and
Medicaid beneficiaries (that is, through
screening, referral, and community
navigation) on their health outcomes
and related healthcare utilization and
costs.88 89 90 91 The AHC Model is one of
the first federal pilots to systematically
test whether identifying and addressing
core HRSNs improves healthcare costs,
utilization, and outcomes with over 600
clinical sites in 21 states.92 The AHC
Model had a 5-year period of
performance that began in May 2017
and ended in April 2022, with
beneficiary screening beginning in the
summer of 2018.93 94 Evaluation of the
AHC Model data is still underway.
Under the AHC Model, the following
five core domains were selected to
screen for HRSNs among Medicare and
Medicaid beneficiaries: (1) food
insecurity; (2) housing instability; (3)
transportation needs; (4) utility
difficulties; and (5) interpersonal safety.
These domains were chosen based upon
literature review and expert consensus
utilizing the following criteria: (1)
availability of high-quality scientific
evidence linking a given HRSN to
adverse health outcomes and increased
healthcare utilization, including
hospitalizations and associated costs; (2)
ability for a given HRSN to be screened
and identified in the inpatient setting
prior to discharge, addressed by
community-based services, and
potentially improve healthcare
outcomes, including reduced
readmissions; and (3) evidence that a
given HRSN is not systematically
addressed by healthcare providers.95 In
addition to established evidence of their
association with health status, risk, and
outcomes, these five domains were
selected because they can be assessed
across the broadest spectrum of
individuals in a variety of settings.96 97 98
These five evidence-based HRSN
domains, which informed development
of the two Social Drivers of Health
measures adopted in the Hospital IQR
Program and finalized here for the
IPFQR Program, are described in Table
18. We note that while the measures
were initially developed by The Health
Initiative (THI), CMS has since assumed
stewardship.
85 The Physicians Foundation. (2019).
Viewpoints: Social Determinants of Health.
Available at: https://physiciansfoundation.org/wpcontent/uploads/2019/08/The-PhysiciansFoundation-SDOH-Viewpoints.pdf. Accessed on
February 20, 2023.
86 Centers for Disease Control and Prevention.
(2020). CDC COVID–19 Response Health Equity
Strategy: Accelerating Progress Towards Reducing
COVID–19 Disparities and Achieving Health Equity.
July 2020. Available at: https://www.cdc.gov/
coronavirus/2019-ncov/community/health-equity/
cdc-strategy.html. Accessed on February 20, 2023.
87 Kaiser Family Foundation. (2021). Racial and
Ethnic Health Inequities and Medicare. Available
at: https://www.kff.org/medicare/report/racial-andethnic-health-inequities-and-medicare/. Accessed
on February 20, 2023.
88 Centers for Medicare & Medicaid Services.
(2021). A Guide to Using the Accountable Health
Communities Health-Related Social Needs
Screening Tool: Promising Practices and Key
Insights. June 2021. Accessed: November 23, 2021.
Available at: https://innovation.cms.gov/media/
document/ahcm-screeningtool-companion.
Accessed on February 20, 2023.
89 Alley, D.E., Asomugha, C.N., et al. (2016).
Accountable Health Communities—Addressing
Social Needs through Medicare and Medicaid. The
New England Journal of Medicine 374(1):8–11.
Available at: https://doi.org/10.1056/
NEJMp1512532. Accessed on February 20, 2023.
90 Billioux, A., Verlander, K., Anthony, S., &
Alley, D. (2017). Standardized Screening for HealthRelated Social Needs in Clinical Settings: The
Accountable Health Communities Screening Tool.
NAM Perspectives, 7(5). Available at: https://
doi.org/10.31478/201705b. Accessed on February
20, 2023.
91 Centers for Medicare & Medicaid Services.
(2021). Accountable Health Communities Model.
Accountable Health Communities Model | CMS
Innovation Center Available at: https://
innovation.cms.gov/innovation-models/ahcm.
Accessed on February 20, 2023.
92 RTI International. (2020). Accountable Health
Communities (AHC) Model Evaluation. Available
at: https://innovation.cms.gov/data-and-reports/
2020/ahc-first-eval-rpt. Accessed on February 20,
2023.
93 RTI International. (2020). Accountable Health
Communities (AHC) Model Evaluation. Available
at: https://innovation.cms.gov/data-and-reports/
2020/ahc-first-eval-rpt. Accessed on February 20,
2023.
94 We note that the model officially concluded in
April 2022, but many awardees have continued
with no-cost extensions to continue utilizing
unspent cooperative agreement funding and all
awardees will conclude by April 2023.
95 Billioux, A., Verlander, K., Anthony, S., &
Alley, D. (2017). Standardized Screening for HealthRelated Social Needs in Clinical Settings: The
Accountable Health Communities Screening Tool.
NAM Perspectives, 7(5). Available at: https://
doi.org/10.31478/201705b. Accessed on February
20, 2023.
96 Billioux, A., Verlander, K., Anthony, S., &
Alley, D. (2017). Standardized Screening for HealthRelated Social Needs in Clinical Settings: The
Accountable Health Communities Screening Tool.
NAM Perspectives, 7(5). Available at: https://
doi.org/10.31478/201705b. Accessed on February
20, 2023.
97 Centers for Medicare & Medicaid Services.
(2021). Accountable Health Communities Model.
Accountable Health Communities Model √ CMS
Innovation Center. Available at: https://
innovation.cms.gov/innovation-models/ahcm.
Accessed on February 20, 2023.
98 Kamyck, D., Senior Director of Marketing.
(2019). CMS releases standardized screening tool
for health-related social needs. Activate Care.
Available at: https://blog.activatecare.com/
standardized-screening-for-health-related-socialneeds-in-clinical-settings-the-accountable-healthcommunities-screening-tool/. Accessed on February
20, 2023.
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99 Berkowitz SA, Seligman HK, Meigs JB, Basu S.
Food insecurity, healthcare utilization, and high
cost: a longitudinal cohort study. Am J Managed
Care. 2018 Sep;24(9):399–404. PMID: 30222918;
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pubmed.ncbi.nlm.nih.gov/30222918/. Accessed on
February 20, 2023.
100 Hill-Briggs, F. (2021). Social Determinants of
Health and Diabetes: A Scientific Review. Diabetes
Care. Available at: https://diabetesjournals.org/
care/article/44/1/258/33180/Social-Determinantsof-Health-and-Diabetes-A. Accessed on February
20, 2023.
101 Seligman, H.K., & Berkowitz, S.A. (2019).
Aligning Programs and Policies to Support Food
Security and Public Health Goals in the United
States. Annual Review of Public Health, 40(1), 319–
337. Available at: https://pubmed.ncbi.nlm.nih.gov/
30444684/. Accessed on February 20, 2023.
102 National Academies of Sciences, Engineering,
and Medicine 2006. Executive Summary: CostBenefit Analysis of Providing Non-Emergency
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National Academies Press. Available at: https://
doi.org/10.17226/23285. Accessed on February 20,
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103 Hill-Briggs, F. (2021). Social Determinants of
Health and Diabetes: A Scientific Review. Diabetes
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care/article/44/1/258/33180/Social-Determinantsof-Health-and-Diabetes-A. Accessed on February
20, 2023.
104 Berkowitz SA, Seligman HK, Meigs JB, Basu
S. Food insecurity, healthcare utilization, and high
cost: a longitudinal cohort study. Am J Managed
Care. 2018 Sep;24(9):399–404. PMID: 30222918;
PMCID: PMC6426124. Available at https://
pubmed.ncbi.nlm.nih.gov/30222918/. Accessed on
February 20, 2023.
105 Dean, E.B., French, M.T., & Mortensen, K.
(2020a). Food insecurity, health care utilization,
and health care expenditures. Health Services
Research, 55(S2), 883–893. Available at: https://
doi.org/10.1111/1475-6773.13283. Accessed on
February 20, 2023.
106 https://ps.psychiatryonline.org/doi/10.1176/
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id=ori:rid:crossref.org&rfr_dat=cr_
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107 Larimer, M.E. (2009). Health Care and Public
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of Housing for Chronically Homeless Persons with
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108 Hill-Briggs, F. (2021, January 1). Social
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109 Henry, M., de Sousa, T., Roddey, C., Gayen,
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110 Larimer, M.E. (2009). Health Care and Public
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Severe Alcohol Problems. JAMA, 301(13), 1349.
Available at: https://doi.org/10.1001/
jama.2009.414.
111 Baxter, A., Tweed, E., Katikireddi, S.,
Thomson, H. (2019). Effects of Housing First
approaches on health and well-being of adults who
are homeless or at risk of homelessness: systematic
review and meta-analysis of randomized controlled
trials. Journal of Epidemiology and Community
Health, 73; 379–387. Available at: https://
jech.bmj.com/content/jech/73/5/379.full.pdf.
112 Housing Instability and Mental Health. UNC
Greensboro. May 7, 2021. Available at: https://
chcs.uncg.edu/housing-instability-mental-health/
#:∼:text=Mental%20health%20is%20
correlated%20with%20housing%20in%20several,
homeless%20population%20in%20
America%20suffer%20a%20mental%20illness.
Accessed on December 7, 2022.
113 National Academies of Sciences, Engineering,
and Medicine 2006. Executive Summary: CostBenefit Analysis of Providing Non-Emergency
Medical Transportation. Washington, DC: The
National Academies Press. Available at: https://
doi.org/10.17226/23285.
114 National Academies of Sciences, Engineering,
and Medicine 2006. Executive Summary: CostBenefit Analysis of Providing Non-Emergency
Medical Transportation. Washington, DC: The
National Academies Press. Available at: https://
doi.org/10.17226/23285.
115 Hill-Briggs, F. (2021, January 1). Social
Determinants of Health and Diabetes: A Scientific
Review. Diabetes Care. Available at: https://
pubmed.ncbi.nlm.nih.gov/33139407/.
116 Billioux, A., Verlander, K., Anthony, S., &
Alley, D. (2017). Standardized Screening for HealthRelated Social Needs in Clinical Settings: The
Accountable Health Communities Screening Tool.
NAM Perspectives, 7(5). Available at: https://
doi.org/10.31478/201705b.
117 Shier, G., Ginsburg, M., Howell, J., Volland, P.,
& Golden, R. (2013). Strong Social Support Services,
Such as Transportation And Help For Caregivers,
Can Lead To Lower Health Care Use And Costs.
Health Affairs, 32(3), 544–551. Available at: https://
doi.org/10.1377/hlthaff.2012.0170.
118 https://www.nami.org/Advocacy/PolicyPriorities/Supporting-Community-Inclusion-andNon-Discrimination/Medicaid-Non-EmergencyMedical-Transportation.
119 Baxter, A., Tweed, E., Katikireddi, S.,
Thomson, H. (2019). Effects of Housing First
approaches on health and well-being of adults who
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As a first step towards leveraging the
opportunity to close equity gaps by
identifying patients’ HRSNs, we
finalized the adoption of two evidencebased measures in the Hospital IQR
Program—the Screening for Social
Drivers of Health measure and the
Screen Positive Rate for Social Drivers
of Health measure (collectively, Social
Drivers of Health measures)—and refer
readers to the FY 2023 IPPS/LTCH PPS
final rule (87 FR 49191 through 49220).
Through adoption in the IPFQR
Program, these two Social Drivers of
Health measures (that is, the Screening
for Social Drivers of Health measure
discussed in this section and the Screen
Positive Rate for Social Drivers of
Health measure discussed in section
VI.D.4 of this final rule) will support
identification of specific risk factors for
inadequate healthcare access and
adverse health outcomes among
patients. We note that these measures
will enable systematic collection of
are homeless or at risk of homelessness: systematic
review and meta-analysis of randomized controlled
trials. Journal of Epidemiology and Community
Health, 73; 379–387. Available at: https://
jech.bmj.com/content/jech/73/5/379.full.pdf.
120 Wright, B.J., Vartanian, K.B., Li, H.F., Royal,
N., & Matson, J.K. (2016). Formerly Homeless
People Had Lower Overall Health Care
Expenditures After Moving into Supportive
Housing. Health Affairs, 35(1), 20–27. Available at:
https://doi.org/10.1377/hlthaff.2015.0393.
121 Billioux, A., Verlander, K., Anthony, S., &
Alley, D. (2017). Standardized Screening for HealthRelated Social Needs in Clinical Settings: The
Accountable Health Communities Screening Tool.
NAM Perspectives, 7(5). Available at: https://
doi.org/10.31478/201705b.
122 Henry M., de Sousa, T., Roddey, C., Gayen, S.,
Bednar, T.; Abt Associates. The 2020 Annual
Homeless Assessment Report (AHAR) to Congress;
Part 1: Point-in-Time Estimates of Homelessness,
January 2021. U.S. Department of Housing and
Urban Development. Accessed November 24, 2021.
Available at: https://www.huduser.gov/portal/sites/
default/files/pdf/2020-AHAR-Part-1.pdf.
123 Larimer, M.E. (2009). Health Care and Public
Service Use and Costs Before and After Provision
of Housing for Chronically Homeless Persons with
Severe Alcohol Problems. JAMA, 301(13), 1349.
Available at: https://doi.org/10.1001/
jama.2009.414.
124 https://ajph.aphapublications.org/doi/abs/
10.2105/AJPH.2013.301680.
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HRSNs data. This activity aligns with
our other efforts beyond the acute care
setting, including the CY 2023 Medicare
Advantage and Part D final rule in
which we finalized the policy requiring
that all Special Needs Plans (SNPs)
include one or more questions on
housing stability, food security, and
access to transportation in their health
risk assessment using questions from a
list of screening instruments specified
in sub-regulatory guidance (87 FR 27726
through 27740) as well as the CY 2023
Physician Fee Schedule (PFS) final rule
in which we adopted the Screening for
Social Drivers of Health measure in the
Merit-based Incentive Payment System
(MIPS) (87 FR 70054 through 70055).
The Social Drivers of Health measures
(as set forth in this section VI.D.3 and
section VI.D.4. of this final rule) will
encourage IPFs to identify patients with
HRSNs, who are known to experience
the greatest risk of poor health
outcomes, thereby improving the
accuracy of high-risk prediction
calculations. Improvement in risk
prediction has the potential to reduce
healthcare access barriers, address the
disproportionate expenditures
attributed to people with greatest risk,
and improve the IPF’s quality of
care.125 126 127 128 Further, these data
could guide future public and private
resource allocation to promote targeted
collaboration among IPFs, health
systems, community-based
organizations, and others in support of
improving patient outcomes. We believe
that this screening is especially
important for IPF patients because
patients with psychiatric conditions
have an increased risk of having
HRSNs.129
125 Baker, M.C., Alberti, P.M., et al. (2021). Social
Determinants Matter for Hospital Readmission
Policy: Insights From New York City. Health
Affairs, 40(4), 645–654. Available at: https://
doi.org/10.1377/hlthaff.2020.01742. Accessed on
February 20, 2023.
126 Hammond, G., Johnston, K., et al. (2020).
Social Determinants of Health Improve Predictive
Accuracy of Clinical Risk Models for
Cardiovascular Hospitalization, Annual Cost, and
Death. Circulation: Cardiovascular Quality and
Outcomes, 13 (6) 290–299. Available at: https://
doi.org/10.1161/CIRCOUTCOMES.120.006752.
Accessed on February 20, 2023.
127 Hill-Briggs, F. (2021). Social Determinants of
Health and Diabetes: A Scientific Review. Diabetes
Care. Available at: https://diabetesjournals.org/
care/article/44/1/258/33180/Social-Determinantsof-Health-and-Diabetes-A. Accessed on February
20, 2023.
128 Jaffrey, J.B., Safran, G.B., Addressing Social
Risk Factors in Value-Based Payment: Adjusting
Payment Not Performance to Optimize Outcomes
and Fairness. Health Affairs Blog, April 19, 2021.
Available at: https://www.healthaffairs.org/do/
10.1377/forefront.20210414.379479/full/. Accessed
on February 20, 2023.
129 Adepoju, OE, Liaw, W, et al. (2022)
Assessment of Unmet Health-Related Social Needs
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In the FY 2023 IPF PPS final rule, we
observed that the Hospital IQR Program
had proposed two Social Drivers of
Health measures and stated that we
would consider these measures for the
IPFQR Program in the future (87 FR
46873). The first of these two measures
is the Screening for Social Drivers of
Health measure, which assesses the
percent of patients admitted to the
hospital who are 18 years or older at
time of admission and are screened for
food insecurity, housing instability,
transportation needs, utility difficulties,
and interpersonal safety.
Utilization of screening tools to
identify the burden of unmet HRSNs
can be a helpful first step for IPFs in
identifying necessary community
partners and connecting individuals to
resources in their communities. We
believe collecting data across the same
five HRSN domains that were screened
under the AHC Model and adopted for
acute care hospitals in the Hospital IQR
Program will illuminate their impact on
health outcomes and disparities and the
healthcare cost burden for IPFs,
particularly for IPFs that serve patients
with disproportionately high levels of
social risk, given that patients with
serious mental illness are especially
vulnerable to and affected by HRSNs. In
addition, data collection in the IPF care
setting could inform meaningful and
sustainable solutions for provider-types
participating in other quality reporting
programs to close equity gaps among the
communities they serve.130 131 132 133 134
For data collection of the Screening
for Social Drivers of Health measure,
Among Patients with Mental Illness Enrolled in
Medicare Advantage. Available at: https://
jamanetwork.com/journals/jamanetworkopen/
fullarticle/2798096. Accessed on December 7, 2022.
130 The Physicians Foundation: 2020 Survey of
America’s Patients, Part Three. Available at: https://
physiciansfoundation.org/wp-content/uploads/
2020/10/2020-Physicians-Foundation-SurveyPart3.pdf.
131 Office of the Assistant Secretary for Planning
and Evaluation (ASPE) (2020). Report to Congress:
Social Risk Factors and Performance Under
Medicare’s Value-Based Purchasing Program
(Second of Two Reports). Available at: https://
aspe.hhs.gov/pdf-report/second-impact-report-tocongress.
132 Billioux, A., Verlander, K., Anthony, S., &
Alley, D. (2017). Standardized Screening for HealthRelated Social Needs in Clinical Settings: The
Accountable Health Communities Screening Tool.
NAM Perspectives, 7(5). Available at: https://
doi.org/10.31478/201705b.
133 Baker, M.C., Alberti, P.M., Tsao, T.Y., Fluegge,
K., Howland, R.E., & Haberman, M. (2021). Social
Determinants Matter for Hospital Readmission
Policy: Insights From New York City. Health
Affairs, 40(4), 645–654. Available at: https://
doi.org/10.1377/hlthaff.2020.01742.
134 De Marchis, E., Knox, M., Hessler, D.,
WillardGrace, R., Oliyawola, JN, et al. (2019).
Physician Burnout and Higher Clinic Capacity to
Address Patients’ Social Needs. The Journal of the
American Board of Family Medicine, 32 (1), 69–78.
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IPFs could use a self-selected screening
tool and collect these data in multiple
ways, which can vary to accommodate
the population they serve and their
individual needs. One example of a
potential screening tool for IPFs to
collect data on the Screening for Social
Drivers Health Measure is the AHC
Model’s standard 10-item AHC HealthRelated Social Needs Screening Tool
(AHC HRSN Screening Tool), which
enables providers to identify HRSNs in
the five core domains (described in
Table 18) among community-dwelling
Medicare, Medicaid, and dually eligible
beneficiaries. The AHC Model,
including its screening tool, was tested
across many care delivery sites in
diverse geographic locations across the
United States. More than one million
Medicare and Medicaid beneficiaries
have been screened using the AHC
HRSN Screening Tool, which was
evaluated psychometrically and
demonstrated evidence of both
reliability and validity, including interrater reliability and concurrent and
predictive validity. Moreover, the AHC
HRSN Screening Tool can be
implemented in a variety of places
where patients seek healthcare,
including inpatient psychiatric
facilities.
The intent of the Screening for Social
Drivers of Health measure is to promote
adoption of HRSN screening by IPFs.
We encourage IPFs to use the screening
as a basis for developing their own
individual action plans (for example,
navigation services and subsequent
referral), as well as an opportunity to
initiate or improve partnerships with
community-based service providers. We
believe that this measure will yield
actionable information to close equity
gaps by encouraging IPFs to identify
patients with HRSNs, with a reciprocal
goal of strengthening linkages between
IPFs and local community-based
partners to promptly connect patients
and families to the support they need.
Both the Screening for Social Drivers
of Health measure and the Screen
Positive Rate for Social Drivers of
Health measure, discussed in VI.D.4. of
this final rule, address our Meaningful
Measures Framework’s 135 quality
priority of ‘‘Work with Communities to
Promote Best Practices of Healthy
Living’’ through the Meaningful
Measures Area of ‘‘Equity of Care.’’
Additionally, pursuant to our
Meaningful Measures 2.0, these Social
Drivers of Health measures address the
135 Centers for Medicare & Medicaid Services.
Meaningful Measures Framework. Available at:
https://www.cms.gov/Medicare/Quality-InitiativesPatient-Assessment-Instruments/
QualityInitiativesGenInfo/CMS-Quality-Strategy.
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equity priority area and align with our
commitment to introduce plans to close
health equity gaps and promote equity
through quality measures, including to
‘‘develop and implement measures that
reflect social and economic
determinants.’’ 136 Development,
proposal, and adoption of these
measures also aligns with our strategic
pillar to advance health equity by
addressing the health disparities that
underlie our health system.137 Further,
inclusion of these measures in the
IPFQR Program aligns with these
measures’ adoption in the Hospital IQR
Program in the FY 2023 IPPS/LTCH
final rule (87 FR 49202 through 49215).
The Screening for Social Drivers of
Health measure (alongside the Screen
Positive Rate for Social Drivers of
Health measure described in section
VI.D.4 of this final rule) will be the first
measurement of social drivers of health
in the IPFQR Program. We believe these
measures are appropriate for
measurement of the quality of care
furnished by IPFs. Screening patients
for HRSNs during inpatient
hospitalization in an IPF will allow
healthcare providers, including IPFs, to
identify and potentially help address
HRSNs for this medically underserved
patient population as part of discharge
planning and contribute to long-term
improvements in patient outcomes.
Identifying and addressing HRSNs for
patients receiving care in IPFs could
have a direct and positive impact on
IPFs’ quality performance because of
improvements in patient outcomes that
could occur when patients’ HRSNs are
reduced. Moreover, collecting aggregate
data on the HRSNs of IPF patient
populations via these measures is
crucial in informing design of future
measures that could enable us to set
appropriate performance targets for IPFs
with respect to closing the gap on health
equity.
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b. Overview of Measure
The Screening for Social Drivers of
Health measure assesses whether an IPF
implements screening for all patients
who are 18 years or older at time of
admission for food insecurity, housing
instability, transportation needs, utility
difficulties, and interpersonal safety. To
report on this measure, IPFs will
provide: (1) the number of inpatients
136 Centers for Medicare & Medicaid Services.
Meaningful Measures 2.0: Moving from Measure
Reduction to Modernization. Available at: https://
www.cms.gov/meaningful-measures-20-movingmeasure-reduction-modernization.
137 Brooks-LaSure, C. (2021). My First 100 Days
and Where We Go From Here: A Strategic Vision
for CMS. Available at: https://www.cms.gov/blog/
my-first-100-days-and-where-we-go-here-strategicvision-cms.
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admitted to the facility who are 18 years
or older at time of admission and who
are screened for all of the five HRSNs
(food insecurity, housing instability,
transportation needs, utility difficulties,
and interpersonal safety); and (2) the
total number of patients who are
admitted to the facility who are 18 years
or older on the date they are admitted.
Measure specifications for the
Screening for Social Drivers of Health
measure, which were available during
the review of the MUC List, are
available at https://mmshub.cms.gov/
sites/default/files/map-hospitalmeasure-specifications-manual2022.pdf.
(1) Measure Calculation
(a) Cohort
The Screening for Social Drivers of
Health measure assesses the total
number of patients aged 18 years and
older, screened for HRSNs (specifically,
food insecurity, housing instability,
transportation needs, utility difficulties,
and interpersonal safety) during an IPF
stay.
(b) Numerator
The numerator of the Screening for
Social Drivers of Health measure
consists of the number of patients
admitted to an IPF stay who are 18 years
or older on the date of admission and
are screened during their IPF stay for all
of the following five HRSNs: food
insecurity, housing instability,
transportation needs, utility difficulties,
and interpersonal safety.
(c) Denominator
The denominator of the Screening for
Social Drivers of Health measure
consists of the number of patients who
are admitted to an IPF stay and who are
18 years or older on the date of
admission. The following patients are
excluded from the denominator: (1)
patients who opt-out of screening; and
(2) patients who are themselves unable
to complete the screening during their
inpatient stay and have no legal
guardian or caregiver able to do so on
the patient’s behalf during their IPF
stay.
(d) Calculation
The Screening for Social Drivers of
Health measure is calculated as the
number of patients admitted to an IPF
stay who are 18 years or older on the
date of admission screened for all five
HRSNs (food insecurity, housing
instability, transportation needs, utility
difficulties, and interpersonal safety)
divided by the number of patients 18
years or older on the date of admission
admitted to the IPF.
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(2) Review by the Measure Applications
Partnership
We included the Screening for Social
Drivers of Health measure on the
publicly available ‘‘List of Measures
Under Consideration for December 1,
2022’’ (MUC List), a list of measures
under consideration for use in various
Medicare programs.138 The CBEconvened MAP Health Equity Advisory
Group reviewed the MUC List including
the Screening for Social Drivers of
Health measure (MUC 2022–053) in
detail on December 6 through 7,
2022.139 The MAP Health Equity
Advisory Group expressed support for
the collection of data related to social
drivers of health, but raised concerns
regarding public reporting of these data
and potential repetition of asking
patients the same questions across
settings.140
In addition, on December 8 through 9,
2022, the MAP Rural Health Advisory
Group reviewed the 2022 MUC List and
the MAP Hospital Workgroup did so on
December 13 through 14, 2022.141 The
MAP Rural Health Advisory Group
noted some potential reporting
challenges including the potential
masking of health disparities that are
underrepresented in some areas and that
sample size and populations served may
be an issue, but expressed that the
Screening for Social Drivers of Health
measure serves as a starting point to
determine where screening is occurring.
The MAP Hospital Workgroup
expressed strong support for the
measure but noted that interoperability
will be important and cautioned about
survey fatigue. The MAP Hospital
Workgroup members conditionally
supported the measure pending: (1)
testing of the measure’s reliability and
validity; (2) endorsement by the CBE; (3)
additional details on how potential tools
map to the individual HRSNs, as well as
best practices; (4) identification of
resources that may be available to assist
patients with identified HRSNs; and (5)
138 Centers for Medicare & Medicaid Services. List
of Measures Under Consideration for December 1,
2022. Available at: https://mmshub.cms.gov/
measure-lifecycle/measure-implementation/prerulemaking/lists-and-reports.
139 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
140 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
141 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
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the measure’s alignment with data
standards, particularly the GRAVITY
project.142 The GRAVITY project’s
mission statement is ‘‘to serve as the
open public collaborative advancing
health and social data standardization
for health equity.’’ 143 Thereafter, the
MAP Coordinating Committee
deliberated on January 24 through 25,
2023, and ultimately voted to uphold
the MAP Hospital Workgroup’s
recommendation to conditionally
support for rulemaking with the same
conditions.144
We believe this measure establishes
an important foundation for prioritizing
the achievement of health equity among
IPFs. Our approach to developing health
equity measures is incremental, and we
believe that health care equity outcomes
in the IPFQR Program will inform future
efforts to advance and achieve health
care equity by IPFs. We additionally
believe this measure to be a building
block that lays the groundwork for a
future meaningful suite of measures that
would assess IPF progress in providing
high-quality healthcare for all patients,
regardless of social risk factors or
demographic characteristics.
(3) CBE Endorsement
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We have not submitted this measure
for CBE endorsement at this time.
Although section 1886(s)(4)(D)(i) of the
Act generally requires that measures
specified by the Secretary must be
endorsed by the entity with a contract
under section 1890(a) of the Act, section
1886(s)(4)(D)(ii) of the Act, states that in
the case of a specified area or medical
topic determined appropriate by the
Secretary for which a feasible and
practical measure has not been endorsed
by the entity with a contract under
section 1890(a) of the Act, the Secretary
may specify a measure that is not so
endorsed as long as due consideration is
given to a measure that has been
endorsed or adopted by a consensus
organization identified by the Secretary.
We reviewed measures endorsed by
consensus organizations and were
unable to identify any other measures
on this topic endorsed by a consensus
organization and therefore, we believe
the exception in section 1886(s)(4)(D)(ii)
of the Act applies.
142 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
143 https://thegravityproject.net/.
144 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
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c. Data Collection, Submission and
Reporting
We believe incremental
implementation of the Screening for
Social Drivers of Health measure, by
permitting one year of voluntary
reporting prior to mandatory reporting,
will allow IPFs who are not yet
screening patients for HRSNs to get
experience with collecting data for this
measure and equally allow IPFs who
already undertake screening efforts to
report data already being collected.
Therefore, we proposed voluntary
reporting of this measure beginning
with the data collected in CY 2024,
which would be reported to CMS in CY
2025, followed by mandatory reporting
beginning with data collected in CY
2025, which would be reported to CMS
in CY 2026 for the FY 2027 payment
determination.
Due to variability across IPFs and the
populations they serve, and in
alignment with the Hospital IQR
Program, we will allow IPFs flexibility
with the selection of tools to screen
patients for food insecurity, housing
instability, transportation needs, utility
difficulties, and interpersonal safety.
Potential sources of these data could
include, for example, administrative
claims data, electronic clinical data,
standardized patient assessments, or
patient-reported data and surveys.
Multiple screening tools for healthrelated social needs (HRSNs) already
exist. For additional information on
resources, we refer readers to evidencebased resources like the Social
Interventions Research and Evaluation
Network (SIREN) website, for example,
for comprehensive information about
the most widely used HRSN screening
tools.145 146 SIREN contains descriptions
of the content and characteristics of
various tools, including information
about intended populations, completion
time, and number of questions.
We encourage IPFs to consider digital
standardized screening tools and refer
readers to the FY 2023 IPPS/LTCH PPS
final rule (87 FR 49207 through 49208)
where we discuss how the use of
certified health information technology
(IT), including but not limited to
certified EHR technology, can support
capture of HRSN information in an
145 Social Interventions Research & Evaluation
Network. (2019). Social Needs Screening Tool
Comparison Table. Available at: https://
sirenetwork.ucsf.edu/tools-resources/resources/
screening-tools-comparison. Accessed January 18,
2021.
146 The Social Interventions Research and
Evaluation Network (SIREN) at University of
California San Francisco was launched in the spring
of 2016 to synthesize, disseminate, and catalyze
research on SDOH and healthcare delivery.
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interoperable fashion so that these data
can be shared across the care continuum
to support coordinated care. We also
encourage readers to learn about the
United States Core Data for
Interoperability (USCDI) standard used
in certified health IT and how this
standard can support interoperable
exchange of health and HRSN
assessment data.147
We proposed that IPFs would report
aggregate data on this measure, that is
IPFs would report aggregated data for
the numerator and the denominator to
CMS (as described in section
VI.D.3.b.(1). of this final rule) but would
not be required to report patient-level
data. IPFs are required to submit
information for chart-abstracted
measures once annually using a CMSapproved web-based data collection tool
available within the HQR System
(previously referred to as the QualityNet
Secure Portal). We refer readers to
section VI.I of this final rule (Form,
Manner, and Timing of Quality Data
Submission) for more details on our
previously finalized data submission
and deadline requirements across
measure types.
We invited public comment on this
proposal.
Comment: Many commenters
supported adoption of the Screening for
Social Drivers of Health measure. Some
commenters stated that screening for
these HRSNs will help IPFs better
understand patients’ needs, improve
care coordination with outpatient and
community resources, increase the
dignity and respect with which patients
are treated, and support development of
patient-centered treatment plans. One
commenter stated that the data collected
through these screenings could help
IPFs shape facility level goals associated
with health equity and empower the
workforce to recognize and eliminate
health disparities. One commenter
specifically supported the flexibility
with respect to tool selection and stated
that this will help IPFs select the
standardized screening instruments
most applicable for their individual
patient populations. Another
commenter stated that discharge will
not lead to positive patient outcomes if
the patient is discharged to unstable
conditions or without the transportation
necessary to access support services.
Response: We thank commenters for
their support of the Screening for Social
Drivers of Health measure. We agree
that HRSNs are critical factors that
147 Office of the National Coordinator for Health
IT (ONC). United States Core Data for
Interoperability. Accessed at: https://
www.healthit.gov/isa/united-states-core-datainteroperability-uscdi.
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impact patient outcomes, and increased
knowledge about patients’ HRSNs will
help IPFs shape goals associated with
health equity. Further, we agree that
collecting these data will help IPFs
improve coordination with outpatient
and community resources to better
deliver patient-centered care. Finally,
we note that these activities would
support IPFs’ execution of
responsibilities related to the required
standard for social services under 42
CFR 482.62(f).
Comment: Several commenters
recommended that CMS conduct
additional testing, specifically in the IPF
setting, to ensure that the measure
addresses the specific needs of the IPF
patient population.
Response: We acknowledge that this
measure was initially developed for the
general acute care setting. While we
recognize the value of measures
undergoing testing and evaluation of
validity and feasibility in the setting for
which they are being adopted, given the
urgency of identifying and addressing
HRSNs described in section VI.D.4.a of
this final rule, and, as there are
currently no other existing measures
that address Screening for Social Drivers
of Health, we believe it is important to
implement this measure as soon as
feasible. We believe that this measure is
equally applicable to freestanding IPFs
and psychiatric units within acute care
facilities as to general acute care
settings, because we believe that
identifying the HRSNs of IPF patients
will be equally valuable in
understanding patients’ needs,
improving care coordination with
outpatient and community resources,
increasing the dignity and respect with
which patients are treated, and
supporting development of patientcentered treatment plans as identifying
the HRSNs of acute care hospital
patients. We note that identifying and
addressing HRSNs is a critical topic for
patients treated in IPFs and that there
are high levels of health disparities
experienced by this patient population.
CMS will monitor measure
implementation and data reporting as
part of standard program and measure
review and will consider updates to the
measure if improvements are identified
through this process.
Comment: Many commenters
expressed concern that this measure has
not received endorsement by the CBE.
Response: While we recognize the
value of measures undergoing review for
potential CBE endorsement, given the
urgency of achieving health equity, we
believe it is important to implement this
measure with voluntary reporting
beginning with the CY 2024 reporting
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period followed by mandatory reporting
beginning with the CY 2025 reporting
period/FY 2027 payment determination.
We note that, under section
1886(s)(4)(D)(ii) of the Act, the Secretary
may specify a measure that is not so
endorsed as long as due consideration is
given to measures that have been
endorsed or adopted by a consensus
organization identified by the Secretary.
We reviewed measures endorsed by
consensus organizations and were
unable to identify any other measures
on this topic endorsed by a consensus
organization, and therefore, we believe
the exception in section 1886(s)(4)(D)(ii)
of the Act applies.
Comment: Many commenters
recommended extending the voluntary
reporting phase for this measure.
Response: Beginning to collect the
data remains imperative as we continue
to build on our strategic pillar to
advance health equity by addressing the
health disparities that underlie our
health system. We therefore have
determined that the proposed voluntary
and mandatory reporting periods
prioritize the urgency of capturing
social drivers of health data and taking
actionable steps towards closing the
health equity gap.
Comment: Some commenters
recommended that CMS defer adoption
of this measure until the Hospital IQR
Program’s voluntary reporting period for
its version of this measure concludes to
allow CMS and IPFs to identify best
practices for screening patients and
collecting HRSNs data in a minimally
burdensome way. Some of these
commenters stated that IPFs often have
fewer resources available for such data
collection relative to acute care
hospitals. Other commenters
recommended engaging IPFs to
voluntarily test the measure to ensure
usability, acceptability, and face validity
are met for this setting.
Response: We acknowledge
commenters’ desire to be able to learn
from the experiences of acute care
hospitals reporting this measure.
Hospitals participating in the Hospital
IQR Program that choose to voluntarily
report this measure will have already
reported data in CY 2024 (87 FR 49207).
Furthermore, the Hospital IQR Program
finalized mandatory reporting of this
measure for the FY 2026 payment
determination (that is data submitted in
CY 2025 representing the CY 2024
performance period) (87 FR 49207).
Given the timing of reporting this
measure in the Hospital IQR Program,
we believe that IPFs will have the
opportunity to learn from the
experiences of acute care hospitals,
including best practices for collecting
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HRSNs data, prior to mandatory
reporting for the IPFQR Program for the
FY 2027 payment determination.
Furthermore, we believe that the
voluntary reporting of CY 2024 data
submitted to CMS in CY 2025 for the
IPFQR Program will provide additional
opportunities to identify minimally
burdensome screening instruments and
data collection practices. Finally, we
note that we will monitor measure
implementation and data reporting as
part of standard program and measure
review and will consider updates to the
measure if improvements are identified
through this process. Therefore, we do
not believe that the benefits of
extending voluntary reporting of this
measure in the IPFQR Program for more
than one year outweigh the potential
detriments associated with delay in
measure adoption that extending the
voluntary reporting period would
require.
Comment: Several commenters had
recommendations related to the
specifications for the Screening for
Social Drivers of Health measure
regarding the frequency and timing of
administering these screenings. One
commenter recommended not requiring
individual patients to be screened more
frequently than once per quarter so that
patients who are readmitted or admitted
to other settings over a short duration
are not repeatedly screened when their
HRSNs are unlikely to have changed.
Another commenter recommended that
for patients who have long stays
(sometimes greater than one year) the
measure should be updated to require
an annual screening and screening at
discharge. This commenter stated that
for these patients screening at discharge
would provide data which would
inform discharge planning.
Response: We understand the
commenters’ concerns, especially given
the frequency of unmet HRSNs among
psychiatric patients, regarding patients
who may be screened frequently, or
whose screening results may change
significantly during their inpatient stay
(such as those patients with long
duration stays). We note that screening
can occur any time during the hospital
admission prior to discharge. Further,
for patients frequently admitted to
inpatient facilities, the IPF could
confirm the current status of any
previously reported HRSNs and inquire
about other HRSNs not previously
reported or that may have changed in
the intervening period. For additional
information on how to apply and report
these screenings, we refer readers to the
Hospital IQR Program’s Frequently
Asked Questions document regarding
this measure in the Hospital IQR
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Program, available at: We will develop
a similar Frequently Asked Questions
document for IPFs as part of providing
educational and training materials; this
document will be conveyed through
routine communication channels to
hospitals, vendors, and QIOs, including,
but not limited to, issuing memos,
emails, and notices on a CMS website.
Comment: Several commenters
recommended additional changes to the
measure specifications. Due to the
sensitive nature of screening for risk of
interpersonal violence, commenters
recommended changes that included
removing this domain from the measure
specifications, and updating the
measure to ensure patient privacy when
responding to this screening question,
either by excluding patients who could
not respond to the question
confidentially, or by ensuring responses
remain hidden in all records and
handouts accessible to patients. One
commenter recommended removing the
exclusion language ‘‘and lack of a
guardian or caregiver available to do so
on the patient’s behalf’’ because such a
guardian or caregiver may provide
inaccurate information about the
patient’s risk of interpersonal violence.
One commenter recommended
excluding patients coming from or being
discharged to long-term care settings
because these patients would be at
lower risk for these five HRSNs.
Another commenter recommended
expanding the measure to include
screening for lack of financial resources.
Response: We have prioritized
selection of the proposed five HRSN
domains based on existing evidence
from both the AHC Model, including
recommendations from a technical
expert panel (TEP) that informed the
initial selection, and emerging evidence
of correlations between given social
drivers of health and worse health
outcomes and social drivers of health
for which interventions have shown
marked improvements in health
outcomes and healthcare utilization (88
FR 21280). Through this process we did
not identify lack of financial resources
as being one of the social drivers of
health that met our criteria for selection
(these criteria are set forth in section
V.D.3.a. of the proposed rule and in
section VI.D.3 of this final rule);
therefore, we did not include it in the
Screening for Social Drivers of Health
measure. We note that while the
Screening for Social Drivers of Health
measure requires screening for the five
identified HRSNs, IPFs may screen for
additional HRSNs that they believe are
relevant for their patient population and
the community in which they serve, and
that standardized screening instruments
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such as those available for screening for
these five HRSNs may also include a
screening for lack of financial resources.
For example, the Accountable Health
Communities screening tool includes
questions for eight supplemental
domains, including financial strain.
Furthermore, we note that this measure
is a first step towards development of a
long-term strategy to integrate social
drivers of health and HRSN data into
quality performance measurement and
is part of our broader commitment to
health equity.
We believe it is imperative that IPFs
screen for all five domains established
in this measure. We understand
commenters’ concerns regarding the
sensitive nature of screening for risk of
interpersonal violence and agree that
patient safety must remain the IPF’s
principal concern. We recommend that
IPFs ensure that patients feel that they
are safe answering questions and
remind patients that they may opt out
of the screening for any reason. We note
that, because IPFs likely are covered
entities under the Health Insurance
Portability and Accountability Act of
1996 (HIPAA) Rules (codified at 45 CFR
parts 160 and 164),148 information
provided by patients in response to
screening for this measure would be
protected health information (PHI).149
Therefore, IPFs are responsible for
adopting reasonable safeguards to
ensure that patients’ PHI is not
impermissibly disclosed contrary to
applicable confidentiality, security, and
privacy laws.
We do not believe it would be
appropriate to remove the exclusion
which would allow a caregiver or
guardian to provide information on a
patient’s behalf if the patient is unable
to do so. While we agree that the
scenario presented by commenters (that
is, a guardian or caregiver may provide
inaccurate information about the
patient’s risk of interpersonal violence)
is possible, we do not believe that the
potential unintended consequence of
capturing inaccurate data for this HRSN
for a small portion of patients outweighs
the potential benefit of capturing
accurate data regarding all of these five
HRSNs for as many patients as possible,
including those who are unable to
respond to the screening without the
assistance of a caregiver or guardian.
Finally, we believe that it is
appropriate to assess the HRSNs of all
eligible patients (that is, patients who
148 For more information on the three HIPAA
rules, we refer readers to the HIPAA for
Professionals site at: https://www.hhs.gov/hipaa/
for-professionals/.
149 https://www.hhs.gov/answers/hipaa/what-isphi/.
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51115
are over 18 years of age at admission
and do not meet the measure’s
exclusion criteria) including patients
being admitted from or discharged to
long-term care settings. While these
patients are at lower risk during their
stay in the long-term care facility, we
believe it is appropriate for the IPF to
assess the patient’s overall risk of unmet
HRSNs. We note, for example, that the
AHC screening instrument assesses the
patient’s HRSNs over the past 12
months for the majority of the HRSNs
included in this tool. Therefore,
screening patients admitted from or
being discharged to long-term care
settings could help identify unmet
HRSNs among this patient population.
We will continue to take all concerns,
comments, and suggestions into account
and will consider them as part of any
potential future modifications to these
measures or potential new measure
development in future notice-andcomment rulemaking.
Comment: One commenter
recommended that the Screening for
Social Drivers of Health measure be
completed by a peer support specialist
to engender trust and create a safe
environment.
Response: We agree with the
commenter that it is important for the
screening for HRSNs to be accomplished
in a way that engenders trust and
creates a safe environment. We
recommend that IPFs evaluate the
requirements for administration (such as
whether the screening instrument can
be administered by peer support
specialists) as part of their instrument
selection process. We note that the AHC
instrument described in section VI.D.3
of this rule allows administration by
clinicians and staff 150 and would allow
administration by peer support
specialists.
Comment: One commenter
recommended aligning SDOH related
measures, including this one, across
programs including programs for the
ambulatory setting (including MIPS).
Response: We agree with the
commenter that addressing patients’
HRSNs is important in all settings in
which patients access care. We note that
this measure was adopted into MIPS in
the CY 2023 Physician Fee Schedule
(PFS) final rule (87 FR 70055) as well as
the Hospital IQR Program in the FY
2023 IPPS/LTCH PPS final rule (87 FR
49215). In addition, we have proposed
to adopt this measure in the PPSExempt Cancer Hospital Quality
Reporting Program in the FY 2024 IPPS/
150 https://nam.edu/standardized-screening-forhealth-related-social-needs-in-clinical-settings-theaccountable-health-communities-screening-tool/.
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LTCH PPS proposed rule (88 FR 27128)
and the End-Stage Renal Disease Quality
Incentive Program in the CY 2024 ESRD
PPS proposed rule (88 FR 42515). We
note that only the IPFQR Program is the
subject of this final rule, and the
commenter’s recommendation is
therefore beyond the scope of this final
rule.
Comment: One commenter
recommended against public reporting
until a standardized, validated
instrument is adopted so the data are
collected using a uniform tool. One
commenter requested that CMS provide
guidance on which available,
standardized assessment instruments
address each of the domains.
Response: We are sensitive to the
concerns raised by commenters about
the lack of clarity about which screening
instrument IPFs should use in order to
screen for HRSNs. We acknowledge the
challenges that lack of standardization
across screening instruments or data
collection practices may introduce in
the consistency of the information
collected across IPFs. While we
acknowledge the potential benefits of a
single screening instrument or
prescribed set of standards, we also
recognize the benefits of providing IPFs
with flexibility to customize screening
and data collection to their local
community contexts and patient
populations, especially in the initial
stages of implementing screening
protocols. We encourage IPFs to
prioritize screening tools that have
undergone thorough testing to ensure
they are accurate and reliable. We
believe that this measure should
promote high-quality screening
practices which, among other things,
ensure accurate identification of unmet
social needs.
For selecting a screening tool, we
suggest that IPFs refer to evidence-based
resources for comprehensive
information about the most widely used
HRSN screening tools. For example, the
Social Interventions Research and
Evaluation Network (SIREN) website,151
housed at the Center for Health and
Community at the University of
California, San Francisco, contains
descriptions of the content and
characteristics of various tools,
including information about intended
populations, completion time, and
number of questions.
Comment: Several commenters stated
that a measurement of whether a
screening occurred does not indicate
whether the needs have been met nor
the impact of these specific HRSNs on
the patient’s health outcomes. Some of
151 https://chc.ucsf.edu/siren.
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these commenters also stated that the
lack of resources faced by IPFs may lead
IPFs to screen for SDOH for which they
are unable to assist patients. These
commenters expressed concern that this
may be frustrating for patients who
would expect the IPF to address these
needs after the screening.
Response: During the development of
both Social Drivers of Health measures,
we gave this topic significant
consideration. The intent of the two
measures is to promote adoption of
screening patients for HRSNs by
healthcare providers as well as taking
action to connect patients who identify
one or more HRSNs with available
resources. Evaluation of the AHC Model
concluded that universal screening may
identify needs that would otherwise
remain undetected.152 While broad
availability of community-based
resources that address patients’ healthrelated social needs would be ideal, we
believe that one of the benefits of
collecting data from screening for
HRSNs will be identification of
opportunities to enable meaningful
action, including prioritizing and
investing in such resources. Beginning
to collect the data on patients’ HRSNs
remains imperative and a crucial step in
developing resources for advancing
health equity. Such data collection has
already allowed some entities to
reallocate resources to address
particular HRSNs that
disproportionately affect a given patient
population or geographic region, as
noted in the FY 2023 IPPS/LTCH PPS
final rule, in which the Hospital IQR
Program adopted these measures (87 FR
49213).
Comment: One commenter requested
clarification of whether the measure
will represent the ‘‘total number’’ of
patients screened for SDOH or the
proportion of patients screened for
SDOH.
Response: IPFs will report the
aggregate numerator for this measure
(that is, the total number of patients
admitted to an IPF stay who are 18 years
or older on the date of admission and
screened for all five HRSNs), and the
aggregate denominator (that is, number
of patients who are admitted to an IPF
stay and who are 18 years or older on
the date of admission). Using these data
and the denominator exclusions (that is,
patients who opt-out of screening and
patients who are themselves unable to
complete the screening during their
inpatient stay and have no legal
152 RTI International. (2020). Accountable Health
Communities (AHC) Model Evaluation. Available
at: https://innovation.cms.gov/data-and-reports/
2020/ahc-first-eval-rpt.
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guardian or caregiver able to do so on
their behalf during their IPF stay), we
will calculate the screening rate (that is,
the proportion of patients screened for
all five SDOH) for this measure.
Comment: One commenter did not
support this measure because of their
concern that the specific HRSNs in the
Screening for Social Drivers of Health
measure are not completely aligned
with the HL7 Gravity Project.
Response: We have prioritized the
five HRSN domains in this measure
based on existing evidence from the
AHC Model including recommendations
from a TEP that informed the initial
selection. We commend additional
initiatives currently underway to
expand capabilities to capture
additional social drivers of health data
elements, including the Gravity Project.
We note that the five domains covered
by the Screening for Social Drivers of
Health measure are included within the
‘‘social risk domains’’ of the Gravity
Project. We support harmonization of
data regarding HRSNs for interoperable
electronic health information exchange
that will meet information exchange
standards.
Comment: One commenter did not
support this measure stating their belief
that there is a lack of evidence that
screening impacts quality of care
provided by IPFs.
Response: We note that the two Social
Drivers of Health measures are derived
from existing evidence from both the
AHC Model and emerging evidence of
correlations between the designated
social drivers of health and higher
healthcare utilization of emergency
departments and hospitals, worse health
outcomes and/or drivers of health for
which interventions have shown
marked improvements in health
outcomes and health care utilization (88
FR 21280).
Comment: One commenter did not
support required reporting of these data
because, while the commenter agreed
that screening for SDOH is important
and should be occurring in the IPF
setting, the commenter expressed
concern that reporting these data is too
burdensome and takes away from
patient care. Another commenter did
not support the Screening for Social
Drivers of Health measure because IPF
stays are typically only a few days, and
the commenter stated their belief that
there is therefore insufficient time to
complete these screenings during the
stay.
Response: While we understand
implementation of HRSN screening
processes and reporting of the SDOH
measures is associated with some
burden, as discussed in sections VII.B.
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and VIII.A of this final rule, we believe
the benefits outweigh the burden, as
screening for and identifying patients’
HRSNs is a critical step towards treating
the whole patient, improving clinical
outcomes, improving equitable care, and
ultimately eliminating disparities in
health outcomes among populations
that have been historically underserved
by the healthcare system.
We note that screening can occur any
time during the IPF admission prior to
discharge and that, for example, the
AHC Screening Tool addresses these 5
HRSNs using a total of 10 questions.
Therefore, we believe that IPFs will be
able to find sufficient time during the
patient’s IPF stay to administer this or
a similar screening tool for SDOH.
Final Decision: After consideration of
the public comments we received, we
are finalizing adoption of the Screening
for Social Drivers of Health measure as
proposed.
4. Adoption of the Screen Positive Rate
for Social Drivers of Health Measure
Beginning With Voluntary Reporting of
CY 2024 Data and Followed by
Mandatory Reporting Beginning With
CY 2025 Data/FY 2027 Payment
Determination
ddrumheller on DSK120RN23PROD with RULES3
a. Background
The impact of social risk factors on
health outcomes has been wellestablished in the
literature.153 154 155 156 157 The Physicians
Foundation reported that 73 percent of
the physician respondents to the 2021
iteration of their annual survey agreed
that social risk factors like housing
instability and food insecurity would
153 Institute of Medicine 2014. Capturing Social
and Behavioral Domains and Measures in
Electronic Health Records: Phase 2. Washington,
DC: The National Academies Press. Available at:
https://doi.org/10.17226/18951.
154 Centers for Medicare & Medicaid Services.
(2021). Accountable Health Communities Model.
Accountable Health Communities Model | CMS
Innovation Center. Available at: https://
innovation.cms.gov/innovation-models/ahcm.
Accessed November 23, 2021.
155 Kaiser Family Foundation. (2021). Racial and
Ethnic Health Inequities and Medicare. Available
at: https://www.kff.org/medicare/report/racial-andethnic-health-inequities-and-medicare/. Accessed
November 23, 2021.
156 Milkie Vu et al. Predictors of Delayed
Healthcare Seeking Among American Muslim
Women, Journal of Women’s Health 26(6) (2016) at
58; Nadimpalli SB, Cleland CM, Hutchinson MK,
Islam N, Barnes LL, Van Devanter N. (2016) The
Association between Discrimination and the Health
of Sikh Asian Indians. Health Psychology, 35(4),
351–355. https://doi.org/10.1037/hea0000268.
157 Office of the Assistant Secretary for Planning
and Evaluation (ASPE). (2020). Report to Congress:
Social Risk Factors and Performance Under
Medicare’s Value-Based Purchasing Program
(Second of Two Reports). Available at: https://
aspe.hhs.gov/pdf-report/second-impact-report-tocongress.
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drive health services demand.158
Recognizing the need for a more
comprehensive approach to eliminating
the health equity gap, we have
prioritized quality measures that would
capture social risk factors and facilitate
assessment of their impact on health
outcomes and disparities and healthcare
utilization and costs.159 160 161
Specifically, in the inpatient setting, we
aim to encourage systematic
identification of patients’ HRSNs (as
defined in section VI.D.3.a. of this final
rule) as part of discharge planning with
the intention of promoting linkages with
relevant community-based services that
address those needs and support
improvements in health outcomes
following discharge from the IPF.
While the Screening for Social Drivers
of Health measure (discussed previously
in section VI.D.3. of this final rule)
enables identification of individuals
with HRSNs, use of the Screen Positive
Rate for Social Drivers of Health
measure would allow IPFs to capture
the magnitude of these needs and even
estimate the impact of individual-level
HRSNs on healthcare utilization when
evaluating quality of care.162 163 164 The
Screen Positive Rate for Social Drivers
of Health measure will require IPFs to
report the rates of patients who screened
158 The Physicians Foundation. (2020) 2020
Survey of America’s Patients, Part Three. Available
at: https://physiciansfoundation.org/wp-content/
uploads/2020/10/2020-Physicians-FoundationSurvey-Part3.pdf.
159 Alley, D.E., C.N. Asomugha, P.H. Conway, and
D.M. Sanghavi. 2016. Accountable Health
Communities–Addressing Social Needs through
Medicare and Medicaid. The New England Journal
of Medicine 374(1):8–11. Available at: https://
doi.org/10.1056/NEJMp1512532.
160 Centers for Medicare & Medicaid Services.
(2021). Accountable Health Communities Model.
Accountable Health Communities Model | CMS
Innovation Center. Available at: https://
innovation.cms.gov/innovation-models/ahcm.
Accessed November 23, 2021.
161 Billioux, A., Verlander, K., Anthony, S., &
Alley, D. (2017). Standardized Screening for HealthRelated Social Needs in Clinical Settings: The
Accountable Health Communities Screening Tool.
NAM Perspectives, 7(5). Available at: https://
doi.org/10.31478/201705b.
162 Baker, M.C., Alberti, P.M., Tsao, T.Y., Fluegge,
K., Howland, R.E., & Haberman, M. (2021). Social
Determinants Matter for Hospital Readmission
Policy: Insights From New York City. Health
Affairs, 40(4), 645–654. Available at: https://
doi.org/10.1377/hlthaff.2020.01742.
163 CMS. Accountable Health Communities
Model. Accountable Health Communities Model |
CMS Innovation Center. Available at: https://
innovation.cms.gov/innovation-models/ahcm.
Accessed November 23, 2021.
164 Hammond, G., Johnston, K., Huang, K., Joynt
Maddox, K. (2020). Social Determinants of Health
Improve Predictive Accuracy of Clinical Risk
Models for Cardiovascular Hospitalization, Annual
Cost, and Death. Circulation: Cardiovascular
Quality and Outcomes, 13 (6) 290–299. Available at:
https://doi.org/10.1161/
CIRCOUTCOMES.120.006752.
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51117
positive for each of the five core HRSNs.
Reporting the screen positive rate for
each of the five core HRSNs will inform
actionable planning by IPFs towards
closing health equity gaps unique to the
populations they serve and enable the
development of individual patient
action plans (including navigation and
referral services).
In the FY 2022 IPF PPS final rule (86
FR 42625 through 42632) and the FY
2023 IPF PPS final rule (87 FR 46865
through 46873), we discussed our
ongoing consideration of potential
approaches that could be implemented
to address health equity through the
IPFQR Program. As a result of the
feedback we received, we identified the
Screen Positive Rate for Social Drivers
of Health measure to help inform efforts
to address health equity.
This measure assesses the percent of
patients admitted to the IPF who are 18
years or older at time of admission who
were screened for HRSNs and who
screen positive for one or more of the
five HRSNs, including food insecurity,
housing instability, transportation
needs, utility difficulties, or
interpersonal safety (reported as five
separate rates).165
We refer readers to section VI.D.3 of
this final rule where we previously
discussed the screening and
identification process resulting in the
selection of these five domains
associated with the Screen for Social
Drivers of Health measure. The
Screening for Social Drivers of Health
measure forms the basis of this Screen
Positive Rate for Social Drivers of
Health measure. That is, the number of
patients screened for all five HRSNs in
the Screening for Social Drivers of
Health measure is the denominator of
the Screen Positive Rate for Social
Drivers of Health measure described
here.
The COVID–19 pandemic
underscored the overwhelming impact
that these five core domains of HRSNs
have on disparities, health risk,
healthcare access, and health outcomes,
including premature mortality.166 167
165 Billioux, A., Verlander, K., Anthony, S., &
Alley, D. (2017). Standardized Screening for Health
Related Social Needs in Clinical Settings: The
Accountable Health Communities Screening Tool.
NAM Perspectives, 7(5). Available at: https://
doi.org/10.31478/201705b.
166 Kaiser Family Foundation. (2021). Racial and
Ethnic Health Inequities and Medicare. Available
at: https://www.kff.org/medicare/report/racial-andethnic-health-inequities-and-medicare/. Accessed
November 23, 2021.
167 Centers for Disease Control and Prevention.
(2019). CDC COVID–19 Response Health Equity
Strategy: Accelerating Progress Towards Reducing
COVID–19 Disparities and Achieving Health Equity.
July 2020. Available at: https://www.cdc.gov/
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Adoption of the Screen Positive Rate for
Social Drivers of Health measure will
encourage IPFs to track prevalence of
specific HRSNs among patients over
time and use the data to stratify risk as
part of quality performance
improvement efforts. This measure may
also prove useful for patients by
providing data transparency and
signifying IPFs’ familiarity, expertise,
and commitment regarding these health
equity issues. This measure also has the
potential to reduce healthcare provider
burden and burnout, including among
IPFs and their staff, by both
acknowledging patients’ non-clinical
needs that nevertheless greatly
contribute to adverse clinical outcomes
and linking providers with communitybased organizations to enhance patientcentered treatment and discharge
planning.168 169 170 Finally, we believe
the Screen Positive Rate for Social
Drivers of Health measure has the
potential to facilitate data-informed
collaboration with community-based
services and focused community
investments, including the development
of pathways and infrastructure to
connect patients to local community
resources.
Ultimately, we are focused on
supporting effective and sustainable
collaboration between healthcare
delivery and local community-based
services organizations to meet the
unmet needs of people they serve.
Reporting data from both the Screening
for Social Drivers of Health and the
Screen Positive Rate for Social Drivers
of Health measures will enable both
identification and quantification of the
levels of unmet HRSNs among
communities served by IPFs. These two
Social Drivers of Health measures
harmonize, as it is important to know
both whether screening occurred and
the results from the screening in order
to develop sustainable solutions. We
believe that there are multiple benefits
to increasing IPFs’ understanding of
their patients’ HRSNs. First, we believe
that this could lead to increased
clinical-community collaborations and
coronavirus/2019-ncov/community/health-equity/
cdc-strategy.html. Accessed November 17, 2021.
168 The Physicians Foundation. (2020). Survey of
America’s Patients, Part Three. Available at: https://
physiciansfoundation.org/wp-content/uploads/
2020/10/2020-Physicians-Foundation-SurveyPart3.pdf.
169 De Marchis, E., Knox, M., Hessler, D.,
WillardGrace, R., Oliyawola, JN, et al. (2019).
Physician Burnout and Higher Clinic Capacity to
Address Patients’ Social Needs. The Journal of the
American Board of Family Medicine, 32 (1), 69–78.
170 Kung, A., Cheung, T., Knox, M., WillardGrace, R., Halpern, J., et.al, (2019). Capacity to
Address Social Needs Affect Primary Care Clinician
Burnout. Annals of Family Medicine. 17 (6), 487–
494. Available at: https://doi.org/10.1370/afm.2470.
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an associated increase in system
capacity and community investments.
Second, we believe this in turn could
yield a net reduction in costly
healthcare utilization by promoting
more appropriate healthcare service
consumption.171
Pursuant to our Meaningful Measures
2.0 Framework and in alignment with
the measures previously adopted for
hospitals participating in the Hospital
IQR Program, the Screen Positive Rate
for Social Drivers of Health measure
will address the equity priority area and
align with our commitment to introduce
plans to close health equity gaps and
promote equity through quality
measures, including to ‘‘develop and
implement measures that reflect social
and economic determinants.’’ 172 Under
our Meaningful Measures Framework,
the Screen Positive Rate for Social
Drivers of Health measure will address
the quality priority of ‘‘Work with
Communities to Promote Best Practices
of Healthy Living’’ through the
Meaningful Measures Area of ‘‘Equity of
Care.’’ 173 Adoption of this measure will
also align with our strategic pillar to
advance health equity by addressing the
health disparities that underlie our
health system.174
b. Overview of Measure
The Screen Positive Rate for Social
Drivers of Health measure is intended to
enhance standardized data collection
that can identify individuals who are at
higher risk for poor health outcomes
related to HRSNs who would benefit
from connection via the IPF to targeted
community-based services.175 The
measure identifies the proportion of
patients admitted to an IPF stay who are
171 Centers for Medicare & Medicaid Services.
(2021). Accountable Health Communities Model.
Accountable Health Communities Model | CMS
Innovation Center. Available at: https://
innovation.cms.gov/innovation-models/ahcm.
Accessed November 23, 2021.
172 Centers for Medicare & Medicaid Services.
Meaningful Measures 2.0: Moving from Measure
Reduction to Modernization. Available at: https://
www.cms.gov/meaningful-measures-20-movingmeasure-reduction-modernization.
173 Centers for Medicare & Medicaid Services.
(2021). CMS Measures Management System
Blueprint (Blueprint v 17.0). Available at: https://
www.cms.gov/Medicare/Quality-Initiatives-PatientAssessment-Instruments/MMS/MMS-Blueprint.
174 Brooks-LaSure, C. (2021). My First 100 Days
and Where We Go From Here: A Strategic Vision
for CMS. Available at: https://www.cms.gov/blog/
my-first-100-days-and-where-we-go-here-strategicvision-cms.
175 Centers for Medicare & Medicaid Services.
(2021). A Guide to Using the Accountable Health
Communities Health-Related Social Needs
Screening Tool: Promising Practices and Key
Insights (June 2021). Available at: https://
innovation.cms.gov/media/document/ahcmscreeningtool-companion. Accessed November 23,
2021.
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18 years or older on the date of
admission to the IPF who screened
positive for one or more of the following
five HRSNs: food insecurity, housing
instability, transportation needs, utility
difficulties, and interpersonal safety.
Consistent with the Hospital IQR
Program, which adopted this measure in
the FY 2023 IPPS/LTCH PPS final rule
(87 FR 49215 through 49220), we will
require IPFs to report this measure as
five separate rates. Specifically, IPFs
will report the number of patients who
screened positive for food insecurity,
the number of patients who screened
positive for housing instability, the
number of patients who screened
positive for transportation needs, the
number of patients who screened
positive for utility difficulties, and the
number of patients who screened
positive for interpersonal safety. We
note that this measure is intended to
provide information to IPFs on the level
of unmet HRSNs among patients served,
and not for comparison between IPFs.
The specifications for the Screen
Positive Rate for Social Drivers of
Health measure, which were available
during the review of the MUC List, are
available at: https://mmshub.cms.gov/
sites/default/files/map-hospitalmeasure-specifications-manual2022.pdf.
(1) Measure Calculation
(a) Cohort
The Screen Positive Rate for Social
Drivers of Health measure is a process
measure that provides information on
the percent of patients, 18 years or older
on the date of admission for an IPF stay,
who were screened for all five
HRSNs,176 and who screen positive for
one or more of the following five
HRSNs: food insecurity; housing
instability; transportation needs; utility
difficulties; or interpersonal safety.
(b) Numerator
The numerator consists of the number
of patients admitted for an IPF stay who
are 18 years or older on the date of
admission, who were screened for an
HRSN, and who screen positive for
having an unmet need in one or more
of the following five HRSNs (calculated
separately): The number of patients who
screened positive for food insecurity,
the number of patients who screened
positive for housing instability, the
number of patients who screened
positive for transportation needs, the
176 We have updated this language to read ‘‘all
five HRSNs’’ as opposed to ‘‘an HRSN’’ to update
the language on the 2022 MUC List: https://
mmshub.cms.gov/sites/default/files/2022-MUCList.xlsx.
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number of patients who screened
positive for utility difficulties, and the
number of patients who screened
positive for interpersonal safety. IPFs
will report the number of patients who
screened positive for having unmet
needs in each of the five HRSNs as a
separate numerator. A patient who
screened positive for more than one
unmet HRSN will be included in the
numerator for each of those HRSNs. For
example, a patient who screened
positive for food insecurity, housing
instability, and transportation needs
would be included in each of these
numerators.
(c) Denominator
The denominator consists of the
number of patients admitted for an IPF
stay who are 18 years or older on the
date of admission and are screened for
all five HRSNs (food insecurity, housing
instability, transportation needs, utility
difficulties and interpersonal safety) 177
during their IPF stay. The following
patients are excluded from the
denominator: (1) patients who opt out of
screening; and (2) patients who are
themselves unable to complete the
screening during their inpatient stay
and have no caregiver able to do so on
the patient’s behalf during their
inpatient stay.
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(d) Calculation
The results of this measure are
calculated as five separate rates. Each
rate is derived from the number of
patients admitted for an IPF stay and
who are 18 years or older on the date
of admission, screened for an HRSN,
and who screen positive for each of the
five HRSNs (that is, the number of
patients who screened positive for food
insecurity, the number of patients who
screened positive for housing
instability, the number of patients who
screened positive for transportation
needs, the number of patients who
screened positive for utility difficulties,
and the number of patients who
screened positive for interpersonal
safety) divided by the number of
patients 18 years or older on the date of
admission screened for all five HRSNs.
The measure is reported as five separate
rates—one for each HRSN, each
calculated with the same denominator.
(2) Review by the Measure Applications
Partnership
We included the Screen Positive Rate
for Social Drivers of Health measure on
177 We have updated this language to read ‘‘all
five HRSNs’’ as opposed to ‘‘an HRSN’’ to update
the language on the 2022 MUC List: https://
mmshub.cms.gov/sites/default/files/2022-MUCList.xlsx.
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the publicly available MUC List, a list
of measures under consideration for use
in various Medicare programs.178 The
CBE-convened MAP Health Equity
Advisory Group reviewed the MUC List
and the Screen Positive Rate for Social
Drivers of Health measure (MUC 2022–
050) in detail on December 6 through 7,
2022.179 The MAP Health Equity
Advisory Group expressed support for
the collection of data related to social
drivers of health, but raised concerns
regarding public reporting of these data
and potential repetition of asking
patients the same questions across
settings.180
In addition, on December 8 through 9,
2022, the MAP Rural Health Advisory
Group reviewed the 2022 MUC List,
which was also reviewed by the MAP
Hospital Workgroup on December 13
through 14, 2022.181 The MAP Rural
Health Advisory Group noted potential
reporting challenges including the
potential masking of health disparities
that are underrepresented in some areas
and that sample size and populations
served may be an issue but also
expressed support that the measure
seeks to advance the drivers of health
and serves as a starting point to
determine where screening is occurring.
The MAP Hospital Workgroup
recommended conditional support of
the measure for rulemaking pending: (1)
endorsement by the CBE to address
reliability and validity concerns; (2)
attentiveness to how results are shared
and contextualized for public reporting;
and (3) examination of any differences
in reported rates by reporting process
(that is, to assess whether reported rates
are the same or different across IPFs and
other facilities that may use different
processes to report their data).182
Thereafter, the MAP Coordinating
Committee deliberated on January 24
178 Centers for Medicare & Medicaid Services. List
of Measures Under Consideration for December 1,
2022. Available at: https://mmshub.cms.gov/
measure-lifecycle/measure-implementation/prerulemaking/lists-and-reports.
179 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
180 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
181 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
182 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
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51119
through 25, 2023, and ultimately voted
to conditionally support the Screen
Positive Rate for Social Drivers of
Health measure for rulemaking with the
same conditions.183
We agree with the MAP Coordinating
Committee’s support for the proposed
Screen Positive Rate for Social Drivers
of Health measure. We believe this
measure, alongside the Screening for
Social Drivers of Health measure,
establishes an important foundation to
prioritizing the achievement of health
equity among IPFs participating in the
IPFQR Program. Our approach to
developing health equity measures is
incremental, and we believe that health
equity outcomes in the IPFQR Program
will inform future efforts to advance and
achieve health equity by IPFs. We
believe this measure to be a building
block that lays the groundwork for a
future meaningful suite of measures that
would assess IPF progress in providing
high-quality healthcare for all patients,
regardless of social risk factors or
demographic characteristics.
(3) CBE Endorsement
We have not submitted this measure
for CBE endorsement at this time.
Although section 1886(s)(4)(D)(i) of the
Act generally requires that measures
specified by the Secretary must be
endorsed by the entity with a contract
under section 1890(a) of the Act, section
1886(s)(4)(D)(ii) of the Act states that in
the case of a specified area or medical
topic determined appropriate by the
Secretary for which a feasible and
practical measure has not been endorsed
by the entity with a contract under
section 1890(a) of the Act, the Secretary
may specify a measure that is not so
endorsed as long as due consideration is
given to a measure that has been
endorsed or adopted by a consensus
organization identified by the Secretary.
We reviewed measures endorsed by
consensus organizations and were
unable to identify any other measures
on this topic endorsed by a consensus
organization; therefore, we believe the
exception in section 1886(s)(4)(D)(ii) of
the Act applies.
c. Data Collection, Submission, and
Reporting
We believe incremental
implementation of the Screen Positive
Rate for Social Drivers of Health
measure, by permitting one year of
voluntary reporting prior to mandatory
reporting, will allow IPFs who are not
183 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
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yet screening patients for HRSNs to get
experience with the measure and
equally allow IPFs who already
undertake screening efforts to report
data already being collected. Therefore,
we proposed voluntary reporting of this
measure, along with the Screening for
Social Drivers of Health measure
described in section VI.D.3 of this final
rule, beginning with the data collected
in CY 2024, which will be reported to
CMS in CY 2025 followed by mandatory
reporting beginning with data collected
in CY 2025, which will be reported to
CMS in CY 2026 and affect FY 2027
payment determination.
While this measure will require IPFs
to collect patient-level data on their
patients’ social drivers of health
screening results, we proposed to adopt
this measure as an aggregate measure
(that is, IPFs would be required to
submit only numerator results for each
of the five screening areas and the
number of patients screened for all five
of the HRSNs). IPFs are required to
submit information for aggregate chartabstracted measures once annually
using a CMS-approved web-based data
collection tool available within the HQR
System (previously referred to as the
QualityNet Secure Portal). We refer
readers to section VI.I of this final rule
(Form, Manner, and Timing of Quality
Data Submission) for more details on
our previously finalized data
submission and deadline requirements
across measure types.
We invited public comment on our
proposal.
We note that we have addressed
comments that broadly referred to both
the Screening for Social Drivers of
Health measure and the Screen Positive
Rate for Social Drivers of Health
measure in the previous section of this
final rule (VI.D.3.).
Comment: Many commenters
supported adoption of the Screen
Positive Rate for Social Drivers of
Health measure. Some commenters
stated that knowing which patients have
each of these HRSNs will help IPFs
better understand patients’ needs,
improve care coordination with
outpatient and community resources,
increase the dignity and respect with
which patients are treated, and support
development of patient-centered
treatment plans.
Response: We thank commenters for
their support of the Screen Positive Rate
for Social Drivers of Health measure. We
agree that HRSNs are critical factors that
impact patient outcomes, and increased
knowledge about patients’ HRSNs will
help IPFs shape goals associated with
health equity. Further, we agree that
collecting these data will help IPFs
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improve coordination with outpatient
and community resources to better
deliver patient-centered care.
Comment: One commenter stated that
access to these data will be useful for
patient advocates to be able to identify
IPFs that are more experienced with
treating patients with more intensive
resource needs.
Response: We agree with the
commenter that publicly reporting these
data might help patients with more
intensive resource needs select IPFs that
are more familiar with treating patients
with that level of need. We note,
however, that the measure is intended
to provide information to IPFs on the
level of unmet need among their
patients and potentially in the
community, and not for comparison
between IPFs (88 FR 21286).
Comment: Some commenters
expressed concern that publicly
reporting these data may lead to
inaccurate perceptions of the quality of
care at IPFs that treat high volumes of
patients who screen positive for one or
more HRSNs. Several of these
commenters stated that IPF patients may
also have more unmet HRSNs than
those at acute care hospitals so the data
may be further misleading if the two
settings are compared.
Response: We appreciate the
commenters’ concerns. The measure is
intended to provide information to IPFs
on the level of unmet need among their
patients and potentially in the
community, and not for comparison
between IPFs (88 FR 21286). We believe
public reporting of healthcare quality
data promotes transparency in the
delivery of care by increasing the
involvement of leadership in healthcare
quality improvement, creating a sense of
accountability, helping to focus
organizational priorities, and providing
a means of delivering important
healthcare information to consumers
and patient advocates. We intend to
conduct outreach and education with
providers and patients to share
information about the two Social
Drivers of Health measures in
conjunction with public reporting.
Comment: One commenter expressed
the belief that reporting five separate
rates, individually reflecting the
proportion of patients who screened
positive for each of the five HRSNs, is
a flawed methodology because it may
not yield reliable and valid
comparisons. Another commenter
expressly supported reporting five
separate rates for this measure to
improve transparency.
Response: We believe that reporting a
separate screen positive rate for each of
the five HRSNs will provide important
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information to IPFs, the communities
that they serve, and policy makers.
Because different community-based
resources are appropriate to address
each of the five HRSNs, we believe that
reporting each of these rates separately
will provide reliable and valid
information to identify which
communities are most in need of which
resources to better enable support in
addressing the most prevalent HRSNs.
Comment: Several commenters
recommended that we develop outcome
measures related to each of the five
HRSNs for future adoption in this and
other quality reporting programs.
Response: We thank commenters for
their feedback. We view the two Social
Drivers of Health measures as a first step
towards development of a long-term
strategy to integrate social drivers of
health data into IPF quality performance
measurement as part of our broader
commitment to health equity. We will
continue to take all comments,
concerns, and suggestions into account
and will consider them as part of any
potential new measure development in
future notice-and-comment rulemaking.
Comment: One commenter requested
clarification on how to define a positive
screening on a tool with a reporting
scale.
Response: Because the reported value
of screening results could vary among
different screening tools or instruments,
we recommend that IPFs carefully
review the supporting materials that
accompany each tool to understand how
to properly administer the instrument
and interpret results when selecting a
screening instrument for their patient
population.
Comment: One commenter did not
support adoption of the Screen Positive
Rate for Social Drivers of Health
measure because the commenter
expressed their belief that only IPFs
would be able to use the data regarding
their patient population and that they
will already have the data from
performing the screening.
Response: We respectfully disagree
and believe that there are multiple
interested parties who will be able to
use data regarding IPFs’ patient
populations, including patients and
their caregivers, patient advocacy
organizations, local community services
organizations, and federal, state, and
local policy makers. We also believe
that the measure will facilitate
systematic gathering of such data in a
manner that provides information to
IPFs on the level of unmet need among
their patients that many IPFs do not
compile currently.
Final Decision: After consideration of
the public comments we received, we
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are finalizing adoption of the Screen
Positive Rate for Social Drivers of
Health measure as proposed.
5. Adoption of the Psychiatric Inpatient
Experience (PIX) Survey Beginning
With Voluntary Reporting of CY 2025
Data Followed by Mandatory Reporting
Beginning With CY 2026 Data/FY 2028
Payment Determination
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a. Background
We believe that a comprehensive
approach to quality must include
directly reported feedback regarding
facility, provider, and payer
performance. Therefore, we have
consistently stated our commitment to
identifying an appropriate patient
experience of care measure for the IPF
setting and adopting this measure in the
IPFQR Program at the first opportunity
(77 FR 53646, 78 FR 50897, 79 FR 45964
through 45965, 80 FR 46714 through
46715, 82 FR 38470 through 38471, 83
FR 38596, 84 FR 38467, 85 FR 47043,
86 FR 42654 through 42656, and 87 FR
46846).
In the FY 2014 IPPS/LTCH PPS final
rule, we adopted a voluntary
information collection regarding
whether IPFs participating in the IPFQR
Program assess patient experience of
inpatient behavioral health services
using a standardized instrument and for
IPFs that answer ‘‘Yes’’ to indicate the
name of the survey that they administer
(78 FR 50896 through 50897). In the FY
2015 IPF PPS final rule, we adopted this
information collection as the
Assessment of Patient Experience of
Care measure beginning with the FY
2016 payment determination (79 FR
45964 through 45965). Data collected for
the FY 2018 payment determination
(that is, data collected in CY 2016)
showed that while the majority of IPFs
(approximately 76 percent) were
collecting patient experience of care
data through a standardized instrument,
there was a wide variation in the
instrument being used. The data for CY
2016 indicated that the most widely
used survey instrument was not in the
public domain and was used by less
than 30 percent of the IPFs that used a
patient experience survey. In the FY
2015 IPF PPS final rule, we indicated
our intention to adopt a standardized
measure of patient experience of care for
the IPFQR Program (79 FR 45964
through 45965).
In the FY 2019 IPF PPS final rule, we
removed the Assessment of Patient
Experience of Care measure from the
IPFQR Program, because we believed
that we had collected sufficient
information to inform development of a
patient experience of care measure (83
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FR 38596 through 38597). In the FY
2020 IPF PPS final rule, we summarized
our analysis of the results of the
Assessment of Patient Experience of
Care measure and requested feedback on
potential adoption of the Hospital
Consumer Assessment of Healthcare
Providers and Systems (HCAHPS)
survey for the IPFQR Program (84 FR
38467). In response to our request, many
commenters expressed concern that the
HCAHPS survey was not specified for
the IPF setting and recommended that
CMS identify a survey that has been
developed for and tested in the IPF
setting. Furthermore, in the FY 2021 IPF
PPS proposed rule, we did not propose
any updates to the IPFQR Program;
however, we received many comments
requesting that we adopt a patient
experience of care measure in the IPFQR
Program, which we summarized in the
FY 2021 IPF PPS final rule (85 FR
47043). We received similar input
strongly advocating for a patient
experience of care measure for the
IPFQR Program in response to a
solicitation of comments on potential
measures for the IPFQR Program in the
FY 2022 IPF PPS proposed rule (86 FR
19511 through 19512), which we
summarized in the FY 2022 IPF PPS
final rule (86 FR 42654 through 42656).
Many of these comments were from
patients and their families and
described how meaningful such a
measure would be for individuals who
receive services from IPFs. Though we
did not solicit input on a patient
experience of care measure in the FY
2023 IPF PPS proposed rule, we
received many comments strongly
recommending that we adopt such a
measure, which we summarized in the
FY 2023 IPF PPS final rule (87 FR
46846). Since publication of the FY
2023 IPF PPS final rule, section 4125(c)
of the Consolidated Appropriations Act,
2023 (Pub. L. 117–328) was enacted,
which amends section 1886(s)(4) of the
Act to require that the quality measures
specified for the IPFQR Program must
include a quality measure of patients’
perspective on care not later than the FY
2031 payment determination.
We have continued to review publicly
available patient experience of care
instruments to identify such an
instrument specified for, and tested in,
the IPF setting. In our review, we
identified the Psychiatric Inpatient
Experience (PIX) survey as a publicly
available survey instrument developed
for and tested in the IPF setting.
Pursuant to the Meaningful Measures
2.0 Framework, this measure addresses
the ‘‘Person-Centered’’ priority area, as
well as the ‘‘Individual and Caregiver
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51121
Voice’’ foundation and aligns with our
commitment to prioritize outcome and
patient-reported measures.184 This
measure also aligns with the CMS
National Quality Strategy Goal 4 ‘‘Foster
Engagement.’’ It also supports the
Behavioral Health Strategy goal of
‘‘Strengthen Equity and Quality in
Behavioral Health Care.’’ 185
Furthermore, this measure supports the
new Universal Foundation domain of
‘‘Person-Centered Care.’’ 186
b. Overview of Measure
The PIX survey was developed by a
team at the Yale University, Yale New
Haven Psychiatric Hospital to address
the gap in available experience of care
surveys, specifically the lack of publicly
available, minimally burdensome,
psychometrically validated surveys
specified for the IPF setting.187 The
interdisciplinary team that developed
this survey, including researchers and
clinicians, conducted the following
steps in developing the survey: (1)
literature review; (2) patient focus
groups; (3) solicitation of input from a
patient and family advisory council; (4)
review of content validity with an
expert panel; (5) development of survey;
and (6) survey testing within the Yale
New Haven Psychiatric Hospital
system.188
The resulting survey contains 23
items in four domains. Patients can
respond to each of the 23 items using a
five-point Likert scale (that is, strongly
disagree, somewhat disagree, neutral,
somewhat agree, strongly agree) or
choose that the item does not apply. The
four domains are:
• Relationship with Treatment Team;
• Nursing Presence;
• Treatment Effectiveness; and
• Healing Environment.189
184 Centers for Medicare & Medicaid Services.
Meaningful Measures 2.0: Moving from Measure
Reduction to Modernization. Available at: https://
www.cms.gov/meaningful-measures-20-movingmeasure-reduction-modernization.
185 CMS. (2022). CMS Behavioral Health Strategy.
Available at https://www.cms.gov/cms-behavioralhealth-strategy. Accessed on February 20, 2023.
186 https://www.nejm.org/doi/full/10.1056/
NEJMp2215539.
187 Klemanski DH, Barnes T, Bautista C, Tancreti
C, Klink B, Dix E. Development and Validation of
the Psychiatric Inpatient Experience (PIX) Survey:
A Novel Measure of Patient Experience Quality
Improvement. Journal of Patient Experience.
2022;9. doi:10.1177/23743735221105671
188 Klemanski DH, Barnes T, Bautista C, Tancreti
C, Klink B, Dix E. Development and Validation of
the Psychiatric Inpatient Experience (PIX) Survey:
A Novel Measure of Patient Experience Quality
Improvement. Journal of Patient Experience.
2022;9. doi:10.1177/23743735221105671.
189 Klemanski DH, Barnes T, Bautista C, Tancreti
C, Klink B, Dix E. Development and Validation of
the Psychiatric Inpatient Experience (PIX) Survey:
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The PIX survey is distributed to
patients by administrative staff at a time
beginning 24 hours prior to planned
discharge. The survey, which is
available in both English and Spanish
and in accessible formats can be
completed prior to discharge using
either a paper copy of the survey or an
electronic version of the survey via
tablet computer.190 For a complete list
of survey questions, including which
questions are elements of each domain,
we refer readers to the description of the
survey in the Journal of Patient
Experience: .
(1) Measure Calculation
(a) Cohort
The cohort for this measure is all
patients discharged from an IPF during
the reporting period who do not meet
one of the following exclusions: (1)
patients who are under 13 years of age
at time of discharge, and (2) patients
who are unable to complete the survey
due to cognitive or intellectual
limitations. The sampling procedures
that IPFs can apply to the PIX survey
measure are described in section VI.I.6
of this final rule.
(b) Calculation
The measure will be reported as five
separate rates, one for each of the four
domains of the PIX survey and one
overall rate. Each of these rates will be
calculated from patient responses on the
PIX survey and then publicly reported
on the Care Compare website (or
successor CMS website). We will report
the mean rates for each domain as well
as the overall mean rate on the Care
Compare website (or successor CMS
website). To calculate the mean scores,
we will assign a numerical value
ranging from 1 (Strongly Disagree) to 5
(Strongly Agree). We will then calculate
the average response by adding the
values of all responses and dividing that
value by the number of responses,
excluding questions that were omitted
or to which the patient selected ‘‘Does
Not Apply.’’
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(2) Review by the Measure Applications
Partnership (MAP)
We included the PIX survey measure
on the publicly available ‘‘List of
Measures Under Consideration for
December 1, 2022’’ (MUC List), a list of
A Novel Measure of Patient Experience Quality
Improvement. Journal of Patient Experience.
2022;9. doi:10.1177/23743735221105671.
190 Klemanski DH, Barnes T, Bautista C, Tancreti
C, Klink B, Dix E. Development and Validation of
the Psychiatric Inpatient Experience (PIX) Survey:
A Novel Measure of Patient Experience Quality
Improvement. Journal of Patient Experience.
2022;9. doi:10.1177/23743735221105671.
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measures under consideration for use in
various Medicare programs.191 The CBEconvened Measure Applications
Partnership (MAP) reviewed the MUC
List and discussed the potential use of
the PIX survey for the IPFQR Program.
The MAP Health Equity Advisory
Group agreed that well-constructed
patient experience of care measures are
an important indicator of quality care.
Overall, the MAP Health Equity
Advisory Group expressed that this
measure is a ‘‘step in the right direction
for behavioral health.’’ 192
In addition, on December 8 through 9,
2022, the MAP Rural Health Workgroup
reviewed the 2022 MUC List and
expressed support for this measure,
with patient support being especially
strong. Some members of the MAP Rural
Health Advisory Group were concerned
about operational challenges,
specifically costs related to
implementation and maintenance and
potential bias if the surveying occurs
prior to discharge.193
The MAP Hospital workgroup
reviewed the 2022 MUC List on
December 13 through 14, 2022. The
MAP Hospital workgroup conditionally
supported the measure for rulemaking,
while emphasizing the importance of
including patient reported experience of
care data in the IPFQR Program. The
MAP Hospital workgroup’s conditions
for support included endorsement by
the CBE and additional testing data for
this measure, specifically: (1) data from
testing of the measure in a variety of
settings (including urban, rural, safety
net providers, and others), (2) data
regarding survey results depending on
the timing of survey administration
(pre- versus post-discharge), (3) data
regarding patient factors (for example,
voluntary versus involuntary
admissions), and (4) data regarding of
mode of administration (for example,
email versus mail) that may affect
performance.194 Thereafter, the MAP
Coordinating Committee deliberated on
191 Centers for Medicare & Medicaid Services. List
of Measures Under Consideration for December 1,
2022. Available at: https://mmshub.cms.gov/
measure-lifecycle/measure-implementation/prerulemaking/lists-and-reports.
192 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
193 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
194 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
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January 24 through 25, 2023 and
ultimately voted to uphold the Hospital
Workgroup’s recommendation to
conditionally support the PIX survey
measure for rulemaking pending the
same conditions as the MAP Hospital
workgroup.195
We believe that the testing that has
been conducted on the PIX survey
demonstrates that it is a valid and
reliable tool for measuring patient
experience of care in IPFs, and that the
results from this initial testing are
generalizable across IPFs. However, we
agree with the MAP Hospital workgroup
that additional testing of this measure
could help better understand measure
results, including any differences in
measure results that were not analyzed
during the PIX survey’s initial testing.
Therefore, the measure developer
intends to conduct additional testing of
the PIX survey prior to public reporting
of the measure data, and we proposed
a voluntary reporting period before
beginning mandatory reporting of the
PIX survey.196
(3) CBE Endorsement
The measure developer has not
submitted this measure for CBE
endorsement at this time. The developer
does intend to submit this measure for
endorsement in the future, following
additional testing as recommended by
the MAP Hospital workgroup. Although
section 1886(s)(4)(D)(i) of the Act
generally requires that measures
specified by the Secretary must be
endorsed by the entity with a contract
under section 1890(a) of the Act, section
1886(s)(4)(D)(ii) of the Act states that in
the case of a specified area or medical
topic determined appropriate by the
Secretary for which a feasible and
practical measure has not been endorsed
by the entity with a contract under
section 1890(a) of the Act, the Secretary
may specify a measure that is not so
endorsed as long as due consideration is
given to a measure that has been
endorsed or adopted by a consensus
organization identified by the Secretary.
We reviewed measures endorsed by
consensus organizations and were
195 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
196 We note that in the FY 2024 IPF PPS proposed
rule we inadvertently stated in section V.5.b.(2)
‘‘Review by the MAP’’ of the proposal that we were
providing a two-year voluntary reporting period (88
FR 21289), which was inconsistent with our
proposal to provide a one-year voluntary reporting
period (88 FR 21290). As noted throughout the
proposed rule, we proposed that voluntary
reporting would begin with CY 2025 data and
mandatory reporting would begin with CY 2026
data. We have corrected the above error here.
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unable to identify any other measures
on this topic endorsed by a consensus
organization. We did identify the
Experience of Care and Health
Outcomes (ECHO) Survey measure (CBE
#008); however, this measure has had its
endorsement removed as of the spring
2020 cycle. Additionally, the ECHO
Survey was developed and tested for
outpatient behavioral health, not the
inpatient setting. Additionally, we
identified the Patient Experience of
Psychiatric Care as Measured by the
Inpatient Consumer Survey (ICS)
measure (CBE #0726). This measure has
also had its endorsement removed as of
the spring 2018 cycle. As neither of
these two measures is endorsed at this
time, we believe the exception in
section 1886(s)(4)(D)(ii) of the Act
applies.
c Data Collection, Submission and
Reporting
IPFs will be responsible for
administering the survey and collecting
data on survey responses, because the
PIX survey is administered beginning 24
hours prior to a patient’s planned
discharge. Therefore, IPFs will collect
the data in a manner similar to the
collection of data for chart-abstracted
measures or other patient screening
measures. That is, the IPFs will collect
data in the facility and then report these
data to CMS using the methods
described in section VI.I.4 of this final
rule, ‘‘Data Submission Requirements,’’
under ‘‘Procedural Requirements.’’
Because we anticipate that many IPFs,
which already administer different
patient experience of care survey
instruments to their patients, will need
to transition to the PIX survey, we
proposed a voluntary reporting period
beginning with data from CY 2025,
which will be reported to CMS in CY
2026. We will then require IPFs to
report data for the PIX survey measure
beginning with data collected during CY
2026, to be reported to CMS during CY
2027 and affecting the FY 2028 payment
determination.
We invited comments on our
proposal.
Comment: Many commenters strongly
supported the PIX survey measure.
These commenters expressed that the
measure addresses a long-standing
measure gap in the IPFQR Program,
which these commenters characterized
as discriminatory, and specifically
supported the PIX survey instrument
because it was developed with input
from people with lived experience in
the IPF setting. Some of these
commenters representing patients and
their families provided descriptions of
their own and their family members’
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lived experiences to explain how
important such a survey opportunity
would be to IPF patients. Some
commenters stated that patients are
especially vulnerable during inpatient
treatment and that psychological
distress can be exacerbated in this
setting. These commenters expressed
that collecting data regarding the
patients’ experiences of care can
improve patient-centered, traumainformed care in which patients are
treated with dignity and respect. Other
commenters stated that formal patient
feedback motivates improved care. One
commenter stated that collection and
public reporting of these data would
assist community-based providers in
identifying IPFs to which to refer
patients. Other commenters stated that
surveying IPF patients regarding their
experience of care is a form of treating
them with dignity and respect,
empowering them, and showing that
their experiences are important. Several
commenters stated that survey data can
be tied to other data sets to support
research. Another commenter expressed
that IPFs will be able to compare
themselves to other IPFs, which could
motivate quality improvement.
Response: We thank commenters for
their support of the PIX survey measure.
We agree that adoption of a patient
experience of care measure for the IPF
setting addresses a long-standing
measure gap, encourages patientcentered care, and shows that we
believe that the patient’s experience is
a critical element of providing quality
care.
Comment: Some commenters
expressed concern regarding measuring
patient experience of care prior to
discharge. Some of these commenters
expressed that patients may feel unsafe
responding honestly at any point prior
to discharge because of a fear of
retaliation for unfavorable responses.
These commenters recommended
providing an option for patients to
respond post-discharge (such as
providing a paper copy of the survey
with a sealable, addressed envelope to
return the survey after completing it).
Another commenter stated that the
setting in which the survey is
administered, and time provided to
complete the survey, could lead to
variation in results and recommended
administering the survey post-discharge.
Many commenters recommended
allowing vendors to collect and report
the data for IPFs. Other commenters
were specifically concerned regarding
the 24 hours prior to discharge time
period for administering the survey.
Some of these commenters stated that
there are many clinical activities
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51123
occurring during this phase of the
patient’s stay and that adding another
step may be burdensome for staff and
patients. Other commenters concerned
about the 24 hour prior to discharge
time period expressed that discharge
timelines are often uncertain, and
therefore it may be difficult to know
when the 24 hours prior to discharge
window has started, especially for
patients with long stays.
Response: We would like to clarify
that, if it is not possible for a patient to
complete the survey prior to discharge,
the facility should provide a sealable,
addressed envelope for the patient to
return the survey following discharge.
This situation could apply in situations
in which the patient would prefer more
time or privacy to complete the survey,
in situations in which there are
competing clinical priorities prior to
discharge, or in situations in which
there is uncertainty regarding the timing
of a patient’s discharge. However, we
caution IPFs that relying exclusively on
the mail-back option may prevent the
IPF from meeting the measure’s
minimum sampling requirements. If the
IPF is able to meet the minimum
sampling requirements and chooses to
use a vendor to receive paper surveys,
aggregate and analyze data provided
through the surveys, or to report these
data to CMS on the IPF’s behalf, that
would be consistent with the measure
methodology and specifications.
Comment: Many commenters
expressed support for surveying patients
regarding their experience of care, but
expressed that they already have tools
or vendors in place and that
transitioning to the PIX survey would be
disruptive. Some commenters
specifically stated that this transition
would disrupt their historical trend
data. One commenter expressed concern
that patients complete too many
experience surveys and recommended
that CMS select one tool based on an
evaluation of all current surveys. Some
commenters expressed a preference for
a CAHPS survey because these surveys
are used in other care settings and are
the core element of the CMS
Foundational Measurement Strategy to
address the person-centered care
domain. Other commenters stated that
patients with primary psychiatric
diagnoses continue to be excluded from
HCAHPS and that, even if this exclusion
were removed, by adopting the PIX
survey, data about patient experience in
an IPF would not be comparable to data
regarding patient experience in general
acute care hospitals. Other commenters
recommended that CMS allow IPFs to
select their own patient experience
instrument provided that it addresses
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the domains addressed by the PIX
survey.
Response: We recognize that many
IPFs already use patient experience of
care survey instruments or vendors to
administer and collect survey
instruments on behalf of IPFs, and that
there is a burden for these IPFs to
transition to a new survey instrument
and administration and collection
process. We further recognize that
historical quality improvement trend
data and analytical processes may be
impacted for these IPFs who already use
other patient experience of care survey
instruments. We considered allowing
IPFs to select their own patient
experience data collection instrument
provided that it addresses the domains
addressed by the PIX survey. However,
we believe that using a single,
standardized instrument to assess
patient experience of care across both
freestanding IPFs and those psychiatric
units in acute care hospitals will
provide comparability of experience
data. We believe that publicly reporting
patient experience of care data that
allows for comparisons between IPFs
will be most meaningful to patients and
their caregivers, and will allow IPFs to
compare their measure results to similar
IPFs as part of their quality
improvement initiative. We understand
commenters’ concern that by adopting a
different patient experience of care
measure in the IPF setting than that for
general acute care hospitals (that is, the
HCAHPS survey) measure results will
not be comparable across these settings,
even if HCAHPS is expanded to patients
with primary psychiatric diagnoses in
the general acute care setting. However,
in response to our previous RFIs about
incorporating a patient experience of
care measure in the IPFQR Program,
many commenters (representing
patients, patient advocates, caregivers,
IPFs, and provider associations)
recommended that we adopt a patient
experience of care measure that was
developed specifically for patients
receiving care in IPFs (84 FR 38467).
These commenters stated that there are
elements of care, such as group therapy,
that are unique to the IPF setting and
stated that a survey for this setting
should specifically address these
elements of care. Because it was
developed specifically for this setting,
with input from patients and their
caregivers, the PIX survey does include
questions regarding these unique
elements of care, whereas the HCAHPS
survey does not.
With respect to concerns regarding
loss of trend data, we have proposed to
adopt the measure for mandatory
reporting beginning with CY 2026 data
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(which will be submitted to CMS in CY
2027 and affect FY 2028 payment
determination) to provide additional
time for IPFs to transition to this new
survey. We wish to clarify that IPFs will
be permitted to add questions to the
survey, so if there are specific metrics
that an IPF wishes to continue tracking,
they will be able to do so. We believe
that IPFs will have sufficient time prior
to when mandatory reporting of this
measure begins with the FY 2028
payment determination to determine
which questions will be most
appropriate to add to the survey without
overburdening patients, or how to
compare results from patient responses
to the PIX survey to those of their
existing surveys.
We believe that the commenter who
referenced the CMS Foundational
Measurement Strategy was referring to
the CMS Universal Foundation,197
which includes setting specific versions
of the Consumer Assessment of
Healthcare Providers and Systems
(CAHPS) survey. We considered
potential adoption of a CAHPS measure
for the IPFQR Program and solicited
comment on this in the FY 2020 IPF
PPS proposed rule (84 FR 16986
through 16987) and summarized the
responses to this request in the FY 2020
IPF PPS final rule (84 FR 38467).
Following our review of the HCAHPS
survey and responses to that request for
information, we determined that the PIX
survey is more appropriate for the
IPFQR Program since it has been
developed and tested specifically for
IPFs and with the input of individuals
with lived experience with care in this
setting. Therefore, while the HCAHPS
survey is appropriate for the general
acute care setting, we believe that the
PIX survey is a more appropriate
instrument for measuring patient
experience of care in the IPF setting.
Comment: Many commenters
expressed concern that the PIX survey
has not been sufficiently tested for
national implementation. These
commenters specifically noted a lack of
testing in diverse geographic settings
(including testing for differences in
performance in urban versus rural
settings), lack of testing which compares
this survey to other inpatient consumer
surveys, lack of information about the
correlation coefficients for the proposed
domains, lack of reliability coefficients
to determine the survey’s internal
consistency, lack of demographic data
regarding patients who respond versus
those who do not, lack of testing among
the forensically and/or involuntarily
197 https://www.cms.gov/aligning-qualitymeasures-across-cms-universal-foundation.
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admitted populations, lack of
longitudinal testing, and lack of testing
with facilities which have an average
length of stay greater than 10 days.
Some commenters recommended
additional testing with volunteer IPFs
prior to implementation as a mandatory
measure. Some of these commenters
recommended postponing mandatory
adoption to ensure sufficient testing.
One commenter expressed concern that
the PIX survey does not clearly connect
questions to key outcomes, and
recommended further research and
testing to identify these connections.
Response: We understand
commenters’ concerns regarding the
testing of the PIX survey measure. We
recognize that this is a relatively new
instrument. We note that the measure
developer is continuing to test this
instrument to further address these
questions and concerns prior to the
national implementation of the measure.
To increase time for testing and to better
identify information that will need to be
provided during education and outreach
sessions prior to public reporting, we
proposed and are adopting mandatory
reporting of this measure for the FY
2028 payment determination, which
would not require IPFs to begin
administering and collecting responses
to the PIX survey until CY 2026.
Comment: Some commenters
expressed concern that this survey
instrument is only available in a limited
number of languages and recommended
translation into additional languages to
improve accessibility for all patients.
Some of these commenters
recommended adding supportive
services to help those with language
barriers or limited health literacy
complete the survey.
Response: The measure developer has
translated the survey from English into
Spanish, Mandarin, and Farsi. The
measure developer is currently working
to translate the survey into other
frequently requested languages
(including, French, Arabic, and
Japanese). For patients who have
language barriers, the measure
developer is currently developing
survey administration guidelines for
best practices in survey administration
to enhance the accessibility of the PIX
survey. These include but are not
limited to screen readers, the use of
visual cueing (for example, using simple
emojis that correspond with the Likert
scale options), and the ability to request
assistance in completing the survey.
Options for phone surveys and the use
of interpreters will also be included in
these guidelines. Finally, the measure
developer will add a question to the
survey to indicate if the survey was
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completed with assistance. We
anticipate that the updated survey will
be available during FY 2023 so that IPFs
can review it during their
implementation planning in advance of
the performance period for voluntary
reporting (that is CY 2025).
Comment: Some commenters
requested clarification regarding
whether facilities could add their own
elements to the survey to maintain
historical trend data regarding questions
that are important among their specific
patient populations. Other commenters
specifically requested the inclusion of a
free-text comment section.
Response: Individual facilities can
add supplemental items to the survey
instrument provided that they do not
amend or remove the key elements of
the PIX survey in order to collect data
for and report on this measure. We note
that IPFs may not factor supplemental
items into existing scoring procedures
as this would affect reliability and
validity of this measure. Furthermore,
we encourage facilities to consider the
number of supplemental questions so as
not to overburden or fatigue patients in
completing the survey instrument.
Comment: One commenter
recommended allowing patients to
complete surveys regularly throughout
their stay.
Response: Although we believe that
this may be unduly burdensome to
patients and create administrative and
logistical burden for facilities, this is not
inconsistent with reporting data on the
PIX survey for this measure if the IPF
only includes data for surveys
administered according to the PIX
survey measure’s guidelines
(specifically, PIX surveys administered
beginning 24 hours prior to discharge)
in the measure results reported to CMS.
Comment: Several commenters
recommended additional questions,
topics, and domains that they believe
would be important to include in a
patient experience of care survey for the
IPF setting. These topics included: (1)
data on racial and ethnic disparities in
diagnosing, treating, and providing care;
(2) addressing patients’ spiritual needs;
(3) progress towards remediating life
circumstances that precipitated the
hospitalization; (4) perceptions of
discharge planning and aftercare; (5)
follow-up appointment availability
(were they offered and scheduled); (6)
staff cultural competency; (7) family
involvement in treatment; (8) nurses’
performance; (9) quantity of food; (10)
overall rating; (11) wait time; and (12)
family and caregiver perspectives.
Response: We note that the PIX
survey was developed by an
interdisciplinary team with input from
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patients and a patient and family
advisory council to address items that
are important to patients in this setting
of care. However, as discussed
previously, individual facilities can add
supplemental items to the survey to
address issues important to their patient
populations or that are significant in the
historical trend data.
Comment: One commenter stated that
frequency measurement (which asks
patients to recall how often something
happened) versus evaluative
measurement (which asks patients to
identify how well their needs were met)
can influence the magnitude of
differences when evaluating patient
experience by race and ethnicity. This
commenter specifically noted that
evaluative measures are typically better
at identifying disparities than
frequency-based measures and
recommended considering this in
developing a survey for this setting.
Response: The PIX survey uses an
evaluative measurement (which asks
patients to evaluate their experience of
their care) approach with a Likert Scale
(that is, strongly disagree, somewhat
disagree, neutral, somewhat agree,
strongly agree, and does not apply)
versus a frequency style of evaluation
(which asks patients to report whether
or how frequently something occurred).
We agree with the commenter that
one strength of the evaluative
measurement approach is the ability to
better identify disparities and detect
inequities and note that this was a factor
in the survey design of the PIX
survey.198
Comment: Many commenters
recommended that the survey be
administered by a peer or advocate to
reduce concerns regarding retaliation.
Response: We appreciate this
recommendation and believe that peer
advocates could assist with survey
administration with minimal training.
The measure developer is currently
developing survey administration
guidelines which will incorporate
information on the appropriate training
for staff (including peer advocates) who
will be responsible for survey
administration. We anticipate that these
guidelines will be available during FY
2023 so that IPFs can review them
during their implementation planning
in advance of the performance period
for voluntary reporting (that is, CY
2025).
Comment: Several commenters had
questions regarding public reporting of
these data for this measure. One
198 Linacre JM. Optimizing rating scale category
effectiveness. J Appl Meas. 2002;3(1):85–106. PMID:
11997586.
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commenter requested clarification
regarding whether the data would be
publicly reported. Another commenter
recommended that the data be
accompanied by patient demographic
and clinical information to allow for
stratification and analysis.
Response: As described in section
VI.H of the FY 2024 IPF PPS proposed
rule, we have an established policy for
publicly displaying the data submitted
by IPFs for the IPFQR Program (88 FR
21299 through 21300). Consistent with
that policy, we intend to publicly report
these data. Specifically, in accordance
with section 1886(s)(4)(E) of the Act,
data that an IPF submits to CMS for the
IPFQR Program will be made publicly
available on a CMS website after
providing the IPF an opportunity to
review the data to be made public. In
the FY 2013 IPPS/LTCH PPS final rule
(77 FR 53653 through 53654), we
adopted procedures for making data
submitted under the IPFQR Program
available to the public, after an IPF has
the opportunity to review such data
prior to public display, as required by
section 1886(s)(4)(E) of the Act. We
adopted modifications to these
procedural requirements in the FY 2014
IPPS/LTCH PPS final rule (78 FR 50897
through 50898), and the FY 2017 IPPS/
LTCH PPS final rule (81 FR 57248
through 57249). Specifically, IPFs will
have a period of 30 days to review and
submit corrections to errors resulting
from CMS calculations prior to the data
being made public.
We agree that the intersectionality of
patient characteristics, including the
categorization of clinical populations
would provide useful information for
researchers and potentially for patients
and caregivers in selecting a facility at
which to receive care. However, we note
that the survey is anonymous and
therefore cannot be linked to patients’
clinical data. The measure developer
specifically omitted clinical
characterizations because of patients’
concerns regarding discrimination,
retaliation, and uncertainty about their
suspected versus diagnosed conditions.
We will consider the appropriateness
and feasibility of including
demographic data with publicly
reported measure results for future
public reporting.
Comment: Several commenters
requested clarification on how the data
would be collected and reported. Some
of these commenters stated that IPFs
with limited technological resources
would find it hard to implement this
survey. Some of these commenters
further stated that without sufficient
technological resources this survey
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would be burdensome for IPFs to
administer.
Response: IPFs will collect data in the
facility and then report these data to
CMS using the methods described in
section VI.I.4 of this final rule, that is
‘‘Data Submission Requirements’’ under
‘‘Procedural Requirements.’’ This aligns
with previously finalized policies for
submitting data on chart-abstracted
measures. We recognize that this may be
burdensome for IPFs; however, given
the importance of including a patient
experience of care measure in the IPFQR
Program, we believe that the benefit of
adopting this measure outweighs this
burden.
Comment: One commenter requested
clarification regarding whether IPFs
would be required to respond to
patients to resolve issues identified in
the PIX survey prior to the patient’s
discharge. Another commenter
expressed concern that patients may
include a threat to self or others in their
survey response which would require
IPFs to review responses to ensure that
such threats were addressed prior to
discharge.
Response: We wish to clarify that the
PIX survey is an anonymous survey.
Therefore, it would not be possible for
IPFs to address input from individual
patients, either prior to or after
discharge. We note that there are no
questions on the PIX survey, which is a
series of 23 items to which patients
respond using a five-point Likert scale
(that is, strongly disagree, somewhat
disagree, neutral, somewhat agree,
strongly agree) or choose that the item
does not apply, that address a patient’s
potential threat to self or others. We
acknowledge the possibility that, during
IPF staff’s administration of the survey,
the patient may express to the staff
member a potential threat to self or
others. However, we believe the IPF will
be able to train its staff to appropriately
respond to and notify clinical and other
staff of the patient’s potential threat to
self or others as with any other situation
where IPF staff interact with IPF
patients.
Comment: One commenter requested
clarification regarding whether
completing the survey would be
mandatory for patients. Another
commenter expressed concern that
behavioral health patients often refuse
to complete surveys.
Response: We agree that some
patients may choose not to complete a
survey. We note that, consistent with
our proposal in the FY 2024 IPF PPS
proposed rule (88 FR 21301), we are
requiring IPFs to develop sampling
plans that ensure that IPFs are able to
submit data for 300 completed PIX
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surveys per year. IPFs would be
required to sample from every month
throughout the entire reporting period
and not stop sampling or curtail ongoing
interview activities once a certain
number of completed surveys has been
attained. We recommend that in
developing sampling plans, IPFs
consider the predicted rate of noncompletion to ensure that they reach
300 completed PIX surveys.
Comment: Several commenters
requested clarification regarding
whether patients would be able to have
assistance, such as from a family
member, friend, or peer support
specialist, to complete the survey if the
patient is unable to complete the survey.
One commenter requested clarification
regarding whether a parent or guardian
would be required to complete the
survey for minors.
Response: The PIX survey is suitable
for individuals of all ages within the
measure cohort, which includes patients
who are 13 or older at time of discharge.
The survey was tested with adolescents
aged 13 to17 and testing found that they
were able to complete it without any
significant differences in scores
compared to adults. Nonetheless, we
understand that some individuals may
require assistance, and patients must be
offered the option to seek help from
staff, a caregiver (including parents or
guardians), or a peer. Additionally, the
measure developer is updating the
survey to include a question asking if
the patient received any assistance
while completing it. We anticipate that
the updated survey will be available
during FY 2023 so that IPFs can review
it during their implementation planning
in advance of the performance period
for voluntary reporting (that is CY 2025)
Comment: Several commenters
expressed concern that the exclusion of
patients who are unable to complete the
survey due to cognitive or intellectual
limitations could lead to subjective
exclusions and create bias in the survey
administration. Several of these
commenters recommended removing
this exclusion, and other commenters
recommended providing standardized
definitions that IPFs could apply.
Response: The measure developer is
currently developing guidelines for best
practices in survey administration to
enhance the accessibility of the PIX
survey and sampling integrity. All
patients, including people with
intellectual and development
disabilities, must have an opportunity to
participate in or benefit from the survey
equal to that afforded to others. We
anticipate that these guidelines will be
available during FY 2023 so that IPFs
can review them during their
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implementation planning in advance of
the performance period for voluntary
reporting (that is, CY 2025). We will
communicate the availability of these
guidelines through regular subregulatory communications.
We note that patients who are unable
to complete the survey unaided on the
basis of a disability must be offered
reasonable modifications, such as the
use of visual cueing (for example, using
simple emojis that correspond with the
Likert scale options). We believe that
inclusivity is a key priority of adopting
a patient experience of care survey and
emphasize the importance of
maximizing accessibility for all patients.
Comment: Several commenters
expressed concern that the data
collected by this survey may not be
sufficient to improve patient experience.
Another commenter requested
clarification regarding whether the
survey has been shown to improve
patient outcomes. One commenter
expressed concern about the Healing
Environment domain in the PIX survey
instrument because regulations and
licensing requirements heavily restrict
the environment of the IPF. One
commenter expressed concern that IPFs
do not have the resources to improve
care based on the results of the PIX
survey.
Response: We believe that a
comprehensive approach to quality
must include directly reported feedback
from patients. We have consistently
stated our commitment to identifying a
patient experience of care measure for
the IPF setting, and in our measure
strategies, including the Meaningful
Measures 2.0 Framework, the CMS
National Quality Strategy, the
Behavioral Health Strategy, and the
Universal Foundation, we have
consistently identified the need for
person-centered care and engagement.
Furthermore, we note that a review of
55 studies found that within these
studies it was more common to find
positive associations between patient
experience and patient safety and
clinical effectiveness than no
associations.199 However, including a
measure of patient experience
demonstrates that a positive patient
experience is an important goal in its
own right. This is supported by
consistently strong patient and caregiver
input requesting such a measure be
adopted in the IPFQR Program and
emphasizing that such a measure is an
important element of showing that we
199 Doyle, c. Lennox, L, and Bell, D. A systematic
review of evidence on the links between patient
experience and clinical safety and effectiveness.
BMJ Open. Available at: https://bmjopen.bmj.com/
content/3/1/e001570.
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believe that IPF patients should be
treated with dignity and respect in an
environment in which their voices
matter as part of a patient-centered care
experience. Additionally, we believe
that having a nationally standardized
patient experience of care measure will
allow IPFs to compare their patient
experience results with the results of
other IPFs. This will allow IPFs to
identify opportunities for improvement,
including to their Healing Environment
score, within the regulatory and
licensure constraints under which IPFs
operate. That is, if other similar IPFs
score higher in the Healing Environment
domain despite operating within the
same regulatory and licensure
constraints, this will highlight the
opportunity for the IPF to improve its
Healing Environment.
Comment: One commenter expressed
concern that the domain names do not
appear to match the substance of the
questions within the domain. This
commenter expressed concern that there
may be overlap or inconsistencies
between the use of ‘‘treatment team’’
and ‘‘nursing team.’’
Response: We appreciate this concern;
however, we believe the domain labels
have been appropriately applied.
Specifically, the four-domain survey
aligned with the theoretical basis of
patient experience and was chosen
through extensive focus group testing.
Further, decisions around domains and
their labels were based on the degree to
which individual items statistically
coalesced around central themes. We
noted that patients in focus groups
rarely distinguished roles among their
care teams. Functionally, medical
providers and social workers operate in
a collaborative framework to guide
treatment and coordinate aftercare.
Thus, questions about patients’
relationships with their treatment team
center around their interactions with
those who provide medical and
therapeutic care. The Nursing Presence
domain was identified as a separate
domain due to the distinctive nature of
nurses’ roles in comprehensively caring
for all patients on the unit in support of
the treatment team. We agree with the
measure developer that this important
distinction merited a separate domain to
represent the unique work of the
varying team members with whom
patients interact.
Comment: Some commenters
expressed concerns that this measure
has not been endorsed by the CBE.
Response: We note that following
additional testing, the measure
developer intends to submit this
measure to the CBE for endorsement.
While we recognize the value of
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measures undergoing CBE endorsement
review, given the urgency of adopting a
patient experience of care measure for
this setting, as there are currently no
CBE-endorsed measures that address
IPF patient experience of care, we
believe it is important to implement this
measure beginning with voluntary
reporting of CY 2025 data followed by
mandatory reporting beginning with CY
2026 data, reported to CMS in CY 2027
and affecting the FY 2028 payment
determination. We note that under
section 1886(s)(4)(D)(ii) of the Act the
Secretary may specify a measure that is
not so endorsed as long as due
consideration is given to measures that
have been endorsed or adopted by a
consensus organization identified by the
Secretary. We reviewed measures
endorsed by consensus organizations
and were unable to identify any other
measures on this topic endorsed by a
consensus organization, and therefore,
we believe the exception in section
1886(s)(4)(D)(ii) of the Act applies.
Comment: One commenter requested
clarification on who developed the
survey, whether it is proprietary, and if
so, how IPFs will obtain licenses to use
the survey.
Response: As described in the FY
2024 IPF PPS proposed rule (88 FR
21288), the PIX survey was developed
by a team at the Yale University, Yale
New Haven Psychiatric Hospital and is
in the public domain. We note that the
measure developer is currently
developing guidelines for best practices
in survey administration, and we
strongly encourage staff who will be
responsible for administering the survey
to review these guidelines as soon as
they become available. Because the
measure developer has made the PIX
survey available in the public domain,
there is no certification or license
required to administer the PIX survey.
Comment: One commenter expressed
concern that there are too many
questions for patients to complete.
Response: We understand the
importance of balancing the number of
survey questions to improve completion
rates with minimal burden to the
patient, while including a sufficient
range of questions to address the most
important aspects of patients’
experiences about the care they
received. We note that the PIX survey
has 23 items, which is comparable to
the number of questions in other patient
experience of care survey instruments.
Specifically, two other surveys which
address inpatient care include the
HCAHPS survey, which has 29
questions, and the Inpatient Consumer
Survey (ICS), which has 28 items.
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Comment: One commenter opposed
adopting this survey in a pay-forperformance program.
Response: We note that the IPFQR
Program is a pay-for-reporting program
(that is, IPFs that comply with all
requirements and submit required data
under the IPFQR Program receive their
full payment update) and that there are
not currently any Medicare pay-forperformance programs (that is, programs
which adjust payment based on the
performance on measures) which
address the IPF setting.
Comment: Some commenters
requested clarification regarding
whether the measure would be scored
with ‘‘top-box’’ scoring or with mean
scores, because the MUC List and the
proposed rule described different
methods.
Response: We considered ‘‘top-box’’
scoring and mean scores as we
identified an approach to adopting and
publicly reporting the PIX survey
measure in the IPFQR Program.
Specifically, we considered modeling
the ‘‘top-box’’ scoring used for reporting
performance on the HCAHPS measure
in which data are reported based on the
percent of respondents who selected the
most positive response (that is, the ‘‘topbox’’). However, we believe that mean
scores (that is, the numerical average
calculated by assigning each response a
numerical value from 1—the least
positive, to 5 the most positive,
summing the scores, and dividing that
value by the number of responses)
provide information that is more
meaningful to patients and their
caregivers who are more likely to be
familiar with mean scores as opposed to
‘‘top-box’’ scores. Therefore, we decided
to propose mean scores, which we
described in the FY 2024 IPF PPS
proposed rule (88 FR 21289). We note
that the MUC list submission
acknowledged the possibility that mean
scores would be useful for reporting
with the statement that ‘‘it may be
useful for the distribution of total Likertscale responses to be made available
during initial implementation.’’
Comment: One commenter expressed
support for reporting separate rates for
each domain in addition to the overall
rate. This commenter stated that this
level of data will improve patient choice
and support IPFs’ quality improvement
efforts.
Response: We thank this commenter
for the support and agree that the
increased level of detail will improve
patient choice and support IPF’s quality
improvement efforts.
Comment: Several commenters
requested clarification regarding
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whether there will be a one-year or twoyear voluntary reporting period.
Response: We wish to clarify that,
consistent with our proposal in the FY
2024 IPF PPS proposed rule (88 FR
21290), there will be a 1-year voluntary
reporting period. IPFs that wish to
participate in the voluntary reporting
period will be able to report CY 2025
data to CMS in CY 2026. Beginning with
CY 2026 data, which will be reported to
CMS in CY 2027, all IPFs will be
required to report these data to CMS and
failure to do so would affect their
payment determination for FY 2028.
Comment: Several commenters
expressed support for adoption of this
measure for voluntary reporting of CY
2025 data in CY 2026 followed by
mandatory reporting beginning with CY
2026 data affecting the FY 2028
payment determination to ensure there
is a patient experience measure in the
IPFQR Program as soon as technically
feasible.
Response: We thank these
commenters for their support.
Final Decision: After consideration of
the public comments we received, we
are finalizing adoption of the PIX survey
measure as proposed.
E. Modification of the COVID–19
Vaccination Coverage Among
Healthcare Personnel (HCP) Measure
Beginning With the Quarter 4 CY 2023
Reporting Period/FY 2025 Payment
Determination
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1. Background
On January 31, 2020, the Secretary of
the Department of Health and Human
Services declared a public health
emergency (PHE) for the United States
in response to the global outbreak of
SARS–COV–2, a novel (new)
coronavirus that causes a disease named
‘‘coronavirus disease 2019’’ (COVID–
19).200 Subsequently, multiple quality
reporting programs including the
Hospital IQR Program (86 FR 45374)
and the IPFQR Program (86 FR 42633
through 42640) adopted the COVID–19
Vaccination Coverage Among
Healthcare Personnel (HCP) measure.
The COVID–19 Vaccination Coverage
Among Healthcare Personnel (HCP)
measure adopted in the IPFQR Program
in the FY 2022 IPF PPS final rule (86 FR
42633 through 42650) requires each IPF
to calculate the percentage of HCP
eligible to work in the IPF for at least
one day during the reporting period,
200 U.S. Dept of Health and Human Services,
Office of the Assistant Secretary for Preparedness
and Response. (2020). Determination that a Public
Health Emergency Exists. Available at: https://
www.phe.gov/emergency/news/healthactions/phe/
Pages/2019-nCoV.aspx.
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excluding persons with
contraindications to the COVID–19
vaccine, who have received a complete
vaccination course against SARS-CoV–2
(86 FR 42633 through 42640).
COVID–19 has continued to spread
domestically and around the world with
more than 103.9 million cases and 1.13
million deaths in the United States as of
June 19,2023.201 In recognition of the
ongoing significance and complexity of
COVID–19, the Secretary renewed the
PHE on April 21, 2020, July 23, 2020,
October 2, 2020, January 7, 2021, April
15, 2021, July 19, 2021, October 15,
2021, January 14, 2022, April 12, 2022,
July 15, 2022, October 13, 2022, January
11, 2023, and February 9, 2023.202
While the PHE status ended on May 11,
2023,203 HHS has stated that the public
health response to COVID–19 remains a
public health priority with a whole of
government approach to combatting the
virus, including through vaccination
efforts.204
In the FY 2022 IPF PPS final rule (86
FR 42633 through 42635) and in our
Revised Guidance for Staff Vaccination
Requirements,205 we stated that
vaccination is a critical part of the
nation’s strategy to effectively counter
the spread of COVID–19. We continue to
believe it is important to incentivize and
track HCP vaccination through quality
measurement across care settings,
including IPFs, in order to protect HCP,
patients, and caregivers, and to help
sustain the ability of HCP to continue
serving their communities throughout
the PHE and beyond.
At the time we issued the FY 2022 IPF
PPS final rule where we adopted the
COVID–19 Vaccination Coverage
Among Healthcare Personnel (HCP)
measure, the Food and Drug
Administration (FDA) had issued
emergency use authorizations (EUAs)
for initial and primary adult vaccines
201 Centers for Disease Control and Prevention.
COVID Data Tracker. Accessed February 13, 2023.
Available at: https://covid.cdc.gov/covid-datatracker/#datatracker-home.
202 U.S. Dept. of Health and Human Services.
Office of the Assistant Secretary for Preparedness
and Response. (2023). Renewal of Determination
that a Public Health Emergency Exists. Available at:
https://aspr.hhs.gov/legal/PHE/Pages/covid1911Jan23.aspx.
203 https://www.whitehouse.gov/wp-content/
uploads/2023/01/SAP-H.R.-382-H.J.-Res.-7.pdf.
204 U.S. Dept. of Health and Human Services. Fact
Sheet: COVID–19 Public Health Emergency
Transition Roadmap. February 9, 2023. Available at:
https://www.hhs.gov/about/news/2023/02/09/factsheet-covid-19-public-health-emergency-transitionroadmap.html.
205 Centers for Medicare & Medicaid Services.
Revised Guidance for Staff Vaccination
Requirements QSO–23–02–ALL. October 26, 2022.
Available at: https://www.cms.gov/files/document/
qs0-23-02-all.pdf.
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manufactured by Pfizer-BioNTech,206
Moderna,207 and Janssen.208 On August
23, 2021, the FDA issued an approval
for the Pfizer-BioNTech vaccine, now
marketed as Comirnaty.209 The FDA
issued approval for the Moderna
vaccine, marketed as Spikevax, on
January 31, 2022 210 and an EUA for the
Novavax adjuvanted vaccine on July 13,
2022.211 The FDA also issued EUAs for
COVID–19 single vaccine booster doses
in September 2021 212 and October
2021 213 for certain populations and in
November 2021 214 for all individuals 18
years of age and older. EUAs were
subsequently issued for a second
vaccine booster dose in March 2022 215
206 Food and Drug Administration. (December
2020). FDA Takes Key Action in Fight Against
COVID–19 By Issuing Emergency Use Authorization
for First COVID–19 Vaccine. Available at: https://
www.fda.gov/news-events/press-announcements/
fda-takes-key-action-fight-against-covid-19-issuingemergency-use-authorization-first-covid-19.
207 Food and Drug Administration. (December
2020). FDA Takes Additional Action in Fight
Against COVID–19 By Issuing Emergency Use
Authorization for Second COVID–19 Vaccine.
Available at: https://www.fda.gov/news-events/
press-announcements/fda-takes-additional-actionfight-against-covid-19-issuing-emergency-useauthorization-second-covid.
208 Food and Drug Administration. (February
2021). FDA Issues Emergency Use Authorization for
Third COVID–19 Vaccine. Available at: https://
www.fda.gov/news-events/press-announcements/
fda-issues-emergency-use-authorization-thirdcovid-19-vaccine.
209 Food and Drug Administration. (August 2021).
FDA Approves First COVID–19 Vaccine. Available
at: https://www.fda.gov/news-events/pressannouncements/fda-approves-first-covid-19vaccine.
210 Food and Drug Administration. (January
2022). Coronavirus (COVID–19) Update: FDA Takes
Key Action by Approving Second COVID–19
Vaccine. Available at: https:/www.fda.gov/newsevents/press-announcements/coronavirus-covid-19update-fda-takes-key-action-approving-secondcovid-19-vaccine.
211 Food and Drug Administration. (July 2022).
Coronavirus (COVID–19) Update: FDA Authorizes
Emergency Use of Novavax COVID–19 Vaccine,
Adjuvanted. Available at: https://www.fda.gov/
news-events/press-announcements/coronaviruscovid-19-update-fda-authorizes-emergency-usenovavax-covid-19-vaccine-adjuvanted.
212 Food and Drug Administration. (September
2021). FDA Authorizes Booster Dose of PfizerBioNTech COVID–19 Vaccine for Certain
Populations. Available at: https://www.fda.gov/
news-events/press-announcements/fda-authorizesbooster-dose-pfizer-biontech-covid-19-vaccinecertain-populations.
213 Food and Drug Administration. (October
2021). Coronavirus (COVID–19) Update: FDA Takes
Additional Actions on the Use of a Booster Dose for
COVID–19 Vaccines. Available at: https://
www.fda.gov/news-events/press-announcements/
coronavirus-covid-19-update-fda-takes-additionalactions-use-booster-dose-covid-19-vaccines.
214 Food and Drug Administration. (November
2021). Coronavirus (COVID–19) Update: FDA
Expands Eligibility for COVID–19 Vaccine Boosters.
Available at: https://www.fda.gov/news-events/
press-announcements/coronavirus-covid-19update-fda-expands-eligibility-covid-19-vaccineboosters.
215 Food and Drug Administration. (March 2022).
Coronavirus (COVID–19) Update: FDA Authorizes
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and for bivalent or ‘‘updated’’ booster
doses in August 2022.216
In the FY 2022 IPF PPS final rule, we
stated that data demonstrating the
effectiveness of COVID–19 vaccines to
prevent asymptomatic infection or
transmission of SARS–COV–2, the novel
(new) coronavirus that causes COVID–
19, were limited (86 FR 42634). While
the impact of COVID–19 vaccines on
asymptomatic infection and
transmission was not yet fully known at
the time of the FY 2022 IPF PPS final
rule, there were robust data available on
COVID–19 vaccine effectiveness across
multiple populations against
symptomatic infection, hospitalization,
and death. Two-dose COVID–19
vaccines from Pfizer-BioNTech and
Moderna had been found to be 88
percent and 93 percent effective against
hospitalization for COVID–19,
respectively, over 6 months for adults
over age 18 without
immunocompromising conditions.217
During a SARS–COV–2 surge in the
spring and summer of 2021, 92 percent
of COVID–19 hospitalizations and 91
percent of COVID–19-associated deaths
were reported among persons not fully
vaccinated.218 Real-world studies of
population-level vaccine effectiveness
indicated similarly high rates of
effectiveness in preventing SARS–COV–
2 infection among frontline workers in
multiple industries, with a 90 percent
effectiveness in preventing symptomatic
and asymptomatic infection from
December 2020 through August 2021.219
Second Booster Dose of Two COVID–19 Vaccines
for Older and Immunocompromised Individuals.
Available at: https://www.fda.gov/news-events/
press-announcements/coronavirus-covid-19update-fda-authorizes-second-booster-dose-twocovid-19-vaccines-older-and.
216 Food and Drug Administration. (August 2022).
Coronavirus (COVID–19) Update: FDA Authorizes
Moderna, Pfizer-BioNTech Bivalent COVID–19
Vaccines for Use as a Booster Dose. Available at:
https://www.fda.gov/news-events/pressannouncements/coronavirus-covid-19-update-fdaauthorizes-moderna-pfizer-biontech-bivalent-covid19-vaccines-use.
217 Centers for Disease Control and Prevention.
(September 24, 2021). Morbidity and Mortality
Weekly Report (MMWR). Comparative Effectiveness
of Moderna, Pfizer-BioNTech, and Janssen (Johnson
& Johnson) Vaccines in Preventing COVID–19
Hospitalizations Among Adults Without
Immunocompromising Conditions—United States,
March-August 2021. Available at: https://cdc.gov/
mmwr/volumes/70/wr/mm7038e1.htm?s_
cid=mm7038e1_w.
218 Centers for Disease Control and Prevention.
(September 10, 2021). Morbidity and Mortality
Weekly Report (MMWR). Monitoring Incidence of
COVID–19 Cases, Hospitalizations, and Deaths, by
Vaccination Status—13 U.S. Jurisdictions, April 4–
July 17, 2021. Available at: https://cdc.gov.mmwr/
volumes/70/wr/mm7037e1.htm.
219 Centers for Disease Control and Prevention.
(August 27, 2021). Morbidity and Mortality Weekly
Report (MMWR). Effectiveness of COVID–19
Vaccines in Preventing SARS–COV–2 Infection
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Vaccines have also been highly effective
in real-world conditions (that is,
vaccines have continued to be highly
effective in conditions other than
clinical trials) at preventing COVID–19
in HCP with up to 96 percent
effectiveness for fully vaccinated HCP,
including those at risk for severe
infection and those in racial and ethnic
groups disproportionately affected by
COVID–19.220 In the presence of high
community prevalence of COVID–19,
residents of nursing homes with low
staff vaccination coverage had cases of
COVID–19-related deaths 195 percent
higher than those among residents of
nursing homes with high staff
vaccination coverage.221 Currently
available data demonstrate that COVID–
19 vaccines are effective and prevent
severe disease, including
hospitalization, and death.
As SARS–COV–2 persists and
evolves, our COVID–19 vaccination
strategy must remain responsive. When
we adopted the COVID–19 Vaccination
Coverage Among HCP measure in the
FY 2022 IPF PPS final rule, we stated
that the need for booster doses of the
COVID–19 vaccine had not been
established and no additional doses had
been recommended (86 FR 42639). We
also stated that we believed the
numerator was sufficiently broad to
include potential future boosters as part
of a ‘‘complete vaccination course’’ and
that the measure was sufficiently
specified to address boosters (86 FR
42639). Since we adopted the COVID–
19 Vaccination Coverage Among HCP
measure in the FY 2022 IPF PPS final
rule, new variants of SARS–COV–2 have
emerged around the world and within
the United States. Specifically, the
Omicron variant (and its related
subvariants) is listed as a variant of
concern by the Centers for Disease
Control and Prevention (CDC) because it
spreads more easily than earlier
variants.222 Vaccine manufacturers have
responded to the Omicron variant by
Among Frontline Workers Before and During
B.1.617.2 (Delta) Variant Predominance—Eight U.S.
Locations, December 2020–August 2021. Available
at: https://cdc.gov/mmwr/volume/70/wr/
mm7034e4.htm
220 Pilishivi, T. et al. (December 2022).
Effectiveness of mRNA Covid-19 Vaccine among
U.S. Health Care Personnel. New England Journal
of Medicine. 2021 Dec 16;385(25):e90. Available
online at: https://pubmed.ncbi.nlm.nih.gov/
34551224/.
221 McGarry BE et al. (January 2022). Nursing
Home Staff Vaccination and Covid-19 Outcomes.
New England Journal of Medicine. 2022 Jan
27;386(4):397–398. Available online at: https://
pubmed.ncbi.nlm.nih.gov/34879189/.
222 Centers for Disease Control and Prevention.
(August 2021). Variants of the Virus. Available at:
https://www.cdc.gov/coronavirus/2019-ncov/
variants/.
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developing bivalent COVID–19
vaccines, which include a component of
the original virus strain to provide broad
protection against COVID–19 and a
component of the Omicron variant to
provide better protection against
COVID–19 caused by the Omicron
variant.223 These booster doses of the
bivalent COVID–19 vaccine have been
shown to increase immune response to
SARS–COV–2 variants, including
Omicron, particularly in individuals
who are more than 6 months removed
from receipt of their primary series.224
The FDA issued EUAs for two bivalent
COVID–19 vaccine booster doses, one
from Pfizer-BioNTech 225 and one from
Moderna,226 and strongly encourages
anyone who is eligible to consider
receiving a booster dose with a bivalent
COVID–19 vaccine to provide better
protection against currently circulating
variants.227 COVID–19 booster doses are
associated with a greater reduction in
infections among HCP and their patients
relative to those who only received
primary series vaccination. One study
showed a rate of breakthrough
infections among HCP who received
only the two-dose regimen of the
COVID–19 vaccine of 21.4 percent
compared to a rate of 0.7 percent among
HCP who received a third dose of the
COVID–19 vaccine.228
Despite the efficacy of COVID–19
vaccination generally, data submitted to
the CDC via the National Healthcare
Safety Network (NHSN) demonstrate
clinically significant variation in booster
dose vaccination rates across facilities,
including IPFs. During the first quarter
of 2022, IPFs reported a median
223 Food and Drug Administration. (November
2022). COVID–19 Bivalent Vaccine Boosters.
224 Chalkias, S et al. (October 2022). A Bivalent
Omicron-Containing Booster Vaccine against Covid19. N Engl J Med 2022; 387:1279–1291. Available
online at: https://www.nejm.org/doi/full/10.1056/
NEJMoa2208343.
225 Food and Drug Administration. (November
2022). Pfizer-BioNTech COVID–19 Vaccines.
Available at: https://www.fda.gov/emergencypreparedness-and-response/coronavirus-disease2019-covid-19/pfizer-biontech-covid-19-vaccines.
226 Food and Drug Administration. (November
2022). Moderna COVID–19 Vaccines. Available at:
https://www.fda.gov/emergency-preparedness-andresponse/coronavirus-disease-2019-covid-19/
moderna-covid-19-vaccines.
227 Food and Drug Administration. (August 2022).
Coronavirus (COVID–19) Update: FDA Authorizes
Moderna, Pfizer-BioNTech Bivalent COVID–19
Vaccines for Use as a Booster Dose. Available at:
https://www.fda.gov/news-events/pressannouncements/coronavirus-covid-19-update-fdaauthorizes-moderna-pfizer-biontech-bivalent-covid19-vaccines-use.
228 Oster Y et al. (May 2022). The effect of a third
BNT162b2 vaccine on breakthrough infections in
health care workers: a cohort analysis. Clin
Microbiol Infect. 2022 May;28(5): 735.e1–735.e3.
Available online at: https://
pubmed.ncbi.nlm.nih.gov/35143997/.
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coverage rate of booster or additional
dose(s) of 19.1 percent, with an
interquartile range of 8.7 percent to 37.9
percent. These data, which show a
performance gap in booster coverage,
indicate that there is opportunity to
improve booster vaccination coverage
among HCP in IPFs.229
We believe that vaccination remains
the most effective means to prevent the
worst consequences of COVID–19,
including severe illness, hospitalization,
and death. Given the availability of
vaccine efficacy data, EUAs issued by
the FDA for bivalent boosters, the
continued presence of SARS–COV–2 in
the United States, and variance among
rates of booster dose vaccination, it is
important to modify the COVID–19
Vaccination Coverage Among HCP
measure to refer explicitly to HCP who
receive primary series and booster
vaccine doses in a timely manner. Given
the persistent spread of COVID–19, we
continue to believe that monitoring and
surveillance of vaccination rates among
HCP is important and provides patients,
beneficiaries, and their caregivers with
information to support informed
decision-making.
Beginning with the fourth quarter of
the CY 2023 reporting period/FY 2025
payment determination, we proposed to
modify the COVID–19 Vaccination
Coverage Among HCP measure in the
IPFQR Program to replace the term
‘‘complete vaccination course’’ with the
term ‘‘up-to-date’’ in the HCP
vaccination definition. We also
proposed to update the numerator to
specify the time frames within which an
HCP is considered ‘‘up-to-date’’ with
recommended COVID–19 vaccines,
including booster doses.
In the FY 2022 IPF PPS final rule (86
FR 42638), we stated, and reiterate now,
that the COVID–19 Vaccination
Coverage Among HCP measure is a
process measure that assesses HCP
vaccination coverage rates. Unlike
outcome measures, process measures do
not assess a particular clinical outcome.
2. Overview of Measure
The proposed COVID–19 Vaccination
Coverage Among HCP measure is a
process measure developed by the CDC
to track COVID–19 vaccination coverage
among HCP in settings such as acute
care facilities, including IPFs, and postacute care facilities.
We refer readers to the FY 2022 IPF
PPS final rule (86 FR 42635 through
42636) for more information on the
229 Measure Applications Partnership (MAP)
Hospital Workgroup Preliminary Analyses.
Available at: https://mmshub.cms.gov/sites/default/
files/map-hospital-measure-specifications-manual2022.pdf.
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initial review of the current COVID–19
Vaccination Coverage Among HCP
measure by the Measure Applications
Partnership (MAP). We included an
updated version of the proposed
modification of the COVID–19
Vaccination Coverage Among HCP
measure on the list of measures under
consideration (MUC List), which is
published annually on behalf of CMS by
the CBE with which the Secretary must
contract as required by section 1890(a)
of the Act, for the 2022 to 2023 prerulemaking cycle for consideration by
the MAP.
In December 2022, the MAP Hospital
Workgroup discussed the proposed
modification of the COVID–19
Vaccination Coverage Among HCP
measure. The MAP Hospital Workgroup
stated that the proposed modification of
the current measure captures ‘‘up-todate’’ vaccination information in
accordance with the CDC’s
recommendations, which have been
updated since their initial development.
Additionally, the MAP Hospital
Workgroup appreciated that the
modified measure’s denominator is
broader and simplified from seven
categories of healthcare personnel to
four.230
During review on December 6 and 7,
2022, the MAP Health Equity Advisory
Group highlighted the importance of
COVID–19 measures and asked whether
the proposed modified measure
excludes individuals with
contraindications to Food and Drug
Administration (FDA) authorized or
approved COVID–19 vaccines, and
whether the measure will be stratified
by demographic factors.231 The CDC, the
measure developer for this measure,
responded to the question regarding
individuals with contraindications by
confirming that HCP with
contraindications to the vaccines are
excluded from the measure
denominator. The CDC further
explained that the modified measure
will not be stratified since the data are
submitted at an aggregate rather than an
individual level.
During review on December 8 through
9, 2022, the MAP Rural Health Advisory
Group expressed concerns about data
collection burden, citing that collection
is performed manually and that small
230 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
231 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
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rural hospitals may not have employee
health software.232 The measure
developer (that is, the CDC)
acknowledged the challenge of getting
adequate documentation and
emphasized the goal to ensure the
measure does not present a burden on
providers. The measure developer also
noted that the model used for this
measure is based on the Influenza
Vaccination Coverage Among HCP
measure (CBE #0431), and it intends to
utilize a similar approach to the
modified COVID–19 Vaccination
Coverage Among HCP measure if
vaccination strategy becomes seasonal.
The modified COVID–19 Vaccination
Coverage Among HCP measure received
conditional support for rulemaking
pending testing indicating the measure
is reliable and valid, and endorsement
by the CBE. The MAP noted that the
previous version of the measure
received endorsement from the CBE
(CBE #3636) 233 and that the CDC
intends to submit the proposed updated
measure for endorsement.
a. Measure Specifications
The modification of the COVID–19
Vaccination Coverage Among HCP
measure will require that IPFs continue
to collect data at least one week each
month for each of the three months in
a quarter.
The denominator is the number of
HCP eligible to work in the facility for
at least one day during the reporting
period, excluding persons with
contraindications to COVID–19
vaccination that are described by the
CDC.234 There are not any changes to
the denominator exclusions for the
current COVID–19 Vaccination
Coverage Among HCP measure, and the
modified COVID–19 Vaccination
Coverage Among HCP measure will
continue to exclude otherwise
denominator-eligible HCPs with
contraindications as defined by the
CDC.235 IPFs report the following four
232 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports.
233 Centers for Medicare & Medicaid Services.
2022–2023 MAP Final Recommendations. Available
at: https://mmshub.cms.gov/measure-lifecycle/
measure-implementation/pre-rulemaking/lists-andreports. and CMS Measures Inventory Tool.
Available at: https://cmit.cms.gov/cmit/#/
MeasureView?variantId=5273§ionNumber=1.
234 Centers for Disease Control and Prevention.
(2022). Contraindications and precautions.
Available at: https://www.cdc.gov/vaccines/covid19/clinical-considerations/interim-considerationsus.html#contraindications.
235 Centers for Disease Control and Prevention.
(2022). Contraindications and precautions.
Available at: https://www.cdc.gov/vaccines/covid-
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categories of HCP to NHSN 236; the first
three categories are included in the
measure denominator:
1. Employees: This category includes
all persons who receive a direct
paycheck from the IPF (that is, on the
IPF’s payroll), regardless of clinical
responsibility or patient contact.
2. Licensed independent practitioners
(LIPs): This category includes
physicians (MD, DO), advanced practice
nurses, and physician assistants who are
affiliated with the IPF but are not
directly employed by it (that is, they do
not receive a paycheck from the IPF),
regardless of clinical responsibility or
patient contact. Post-residency fellows
are also included in this category if they
are not on the IPF’s payroll.
3. Adult students/trainees and
volunteers: This category includes
medical, nursing, or other health
professional students, interns, medical
residents, or volunteers aged 18 or older
who are affiliated with the healthcare
facility, but are not directly employed
by it (that is, they do not receive a
paycheck from the facility), regardless of
clinical responsibility or patient contact.
4. Other contract personnel: Contract
personnel are defined as persons
providing care, treatment, or services at
the IPF through a contract who do not
fall into any of the previously discussed
denominator categories. Please note that
this also includes vendors providing
care, treatment, or services at the facility
who may or may not be paid through a
contract. Facilities are required to enter
data on other contract personnel for
submission in the NHSN application,
but reporting for this category is not
included in the COVID–19 Vaccination
Coverage Among HCP measure.
The numerator is the cumulative
number of HCP in the denominator
population who are ‘‘up-to-date’’ with
CDC recommended COVID–19 vaccines.
IPFs would refer to the CDC’s guidance,
to determine the then-applicable
definition of ‘‘up-to-date,’’ as of the first
day of the applicable reporting quarter.
The CDC’s guidance can be found at:
https://www.cdc.gov/nhsn/pdfs/hps/
covidvax/UpToDateGuidance-508.pdf.
For purposes of NHSN surveillance, the
CDC used the following definition of
‘‘up-to-date’’ during the fourth quarter
of CY 2022 surveillance period
(September 26, 2022 through December
25, 2022):
1. Individuals who received an
updated bivalent 237 booster dose, or
19/clinical-considerations/interim-considerationsus.html#contraindications.
236 https://www.cdc.gov/nhsn/pdfs/nqf/covid-vaxhcpcoverage-rev-2023-508.pdf.
237 The updated (bivalent) Moderna and PfizerBioNTech boosters target the most recent Omicron
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2a. Individuals who received their last
booster dose less than 2 months ago, or
2b. Individuals who completed their
primary series 238 less than 2 months
ago.
Subsequent to the publication of the
FY 2024 IPF PPS proposed rule, the
CDC has updated the definition of ‘‘upto-date’’ for the second quarter of CY
2023 surveillance period:
1. Individuals who received an
updated bivalent 239 booster dose, or
2. Individuals who completed their
primary series 240 less than 2 months
ago.
We refer readers to https://
www.cdc.gov/nhsn/nqf/ for
more details on the modified measure
specifications.
We proposed that public reporting of
the modified version of the COVID–19
Vaccination Coverage Among HCP
measure would begin with the October
2024 Care Compare refresh, or as soon
as technically feasible after that refresh.
b. CBE Endorsement
The current version of the COVID–19
Vaccination Coverage Among HCP
measure received CBE endorsement
(CBE #3636, ‘‘Quarterly Reporting of
COVID–19 Vaccination Coverage
Among Healthcare Personnel’’) on July
26, 2022.241
Although section 1886(s)(4)(D)(i) of
the Act generally requires that measures
specified by the Secretary must be
endorsed by the entity with a contract
under section 1890(a) of the Act, section
1886(s)(4)(D)(ii) of the Act states that in
the case of a specified area or medical
topic determined appropriate by the
Secretary for which a feasible and
practical measure has not been endorsed
by the entity with a contract under
section 1890(a) of the Act, the Secretary
may specify a measure that is not so
endorsed as long as due consideration is
given to a measure that has been
subvariants. The updated (bivalent) boosters were
recommended by the CDC on 9/2/2022. As of this
date, the original, monovalent mRNA vaccines are
no longer authorized as a booster dose for people
ages 12 years and older.
238 Completing a primary series means receiving
a two-dose series of a COVID–19 vaccine or a single
dose of Janssen/J&J COVID–19 vaccine.
239 The updated (bivalent) Moderna and PfizerBioNTech boosters target the most recent Omicron
subvariants. The updated (bivalent) boosters were
recommended by the CDC on 9/2/2022. As of this
date, the original, monovalent mRNA vaccines are
no longer authorized as a booster dose for people
ages 12 years and older.
240 Completing a primary series means receiving
a two-dose series of a COVID–19 vaccine or a single
dose of Janssen/J&J COVID–19 vaccine.
241 CMS Measures Inventor Tool. COVID–19
Vaccination Coverage among Healthcare Personnel.
Available at: https://cmit.cms.gov/cmit/#/
MeasureView?variantId=5273§ionNumber=1.
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51131
endorsed or adopted by a consensus
organization identified by the Secretary.
We reviewed measures endorsed by
consensus organizations and were
unable to identify any other measures
on this topic endorsed by a consensus
organization; therefore, we believe the
exception in section 1886(s)(4)(D)(ii) of
the Act applies. The CDC, as the
measure developer, is currently
pursuing endorsement for the modified
version of the measure as the current
version of the measure has already
received endorsement.
3. Data Collection, Submission, and
Reporting
We refer readers to the FY 2022 IPF
PPS final rule (86 FR 42636 through
42640) for information on data
submission and reporting of the current
COVID–19 Vaccination Coverage
Among HCP measure. While we did not
propose any changes to the data
submission or reporting process, we
proposed that reporting of the updated
modified measure would begin with the
fourth quarter of CY 2023 reporting
period for FY 2025 payment
determination. Beginning with the FY
2026 payment determination, we
proposed that IPFs would be required to
submit data for the modified measure
for the entire calendar year.
Under the data submission and
reporting process, IPFs collect the
numerator and denominator for the
COVID–19 Vaccination Coverage
Among HCP measure for at least one
self-selected week during each month of
the reporting quarter and submit the
data to the CDC’s National Health Safety
Network (NHSN) Healthcare Personnel
Safety (HPS) Component before the
quarterly deadline. If an IPF submits
more than one week of data in a month,
the CDC would use most recent week’s
data to calculate the measure results
which would be publicly reported. Each
quarter, the CDC calculates a single
quarterly COVID–19 HCP vaccination
coverage rate for each IPF, which is
calculated by taking the average of the
data from the three weekly rates
submitted by the IPF for that quarter.
CMS publicly reports each quarterly
COVID–19 HCP vaccination coverage
rate as calculated by the CDC based on
the data IPFs submit to the NHSN (86
FR 42636 through 42640).
We invited public comment on our
proposal.
Comment: Some commenters
supported the proposed modification to
the COVID–19 Vaccination Coverage
Among HCP measure. One of these
commenters stated that the modified
specifications would lead to increased
vaccination and booster adoption among
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HCP. One commenter stated that
patients with mental illness are more
vulnerable to COVID–19 driving the
increased need for their providers to be
vaccinated.
Response: We thank the commenters
for their support. We agree that
vaccination plays a critical part of the
nation’s strategy to effectively counter
the spread of COVID–19. We continue to
believe it is important to incentivize and
track rates of vaccination among HCP
through quality measurement across
care settings, including the IPF setting,
in order to protect healthcare workers,
patients, and caregivers, and to help
sustain the ability of HCP in each of
these care settings to continue serving
their communities.
Comment: Several commenters did
not support updating the specifications
for the COVID–19 Vaccination Coverage
Among HCP measure because the PHE
has expired and the Conditions of
Participation (COPs) for hospitals have
been revised to no longer require
reporting of these data. Some of these
commenters requested clarification
regarding whether the change in COPs
means that we will remove the measure
from our quality reporting programs.
One commenter expressed concern that
retaining measurement of COVID–19
Vaccination Coverage Among HCP after
the vaccination requirement has been
removed from COPs sends an
inconsistent message regarding CMS’s
priorities.
Response: As commenters noted, the
PHE for COVID–19 expired on May 11,
2023.242 Since May 11, 2023, some state
and federal reporting requirements have
changed. While CMS requirements for
Medicare and Medicaid-certified
providers and suppliers to ensure that
their staff were fully vaccinated for
COVID–19 have ended with the
expiration of the COVID–19 PHE (88 FR
36488), CMS revised the hospital and
critical access hospitals (CAHs)
infection prevention and control
Condition of Participation so that
hospitals and CAHs will continue to
report on a reduced number of COVID–
19 data elements after the conclusion of
the COVID- 19 PHE until April 30, 2024,
unless the Secretary establishes an
earlier end date.243 While these changes
may impact certain aspects of facility
reporting on COVID–19 data, we note
242 U.S. Dept. of Health and Human Services. Fact
Sheet: COVID–19 Public Health Emergency
Transition Roadmap. February 9, 2023. Available at:
https://www.hhs.gov/about/news/2023/02/09/factsheet-covid-19-public-health-emergency-transitionroadmap.html.
243 https://www.hhs.gov/about/news/2023/05/09/
fact-sheet-end-of-the-covid-19-public-healthemergency.html.
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that the reporting requirements of the
IPFQR Program are distinct from those
related to the expiration of the COVID–
19 PHE and facilities participating in
the IPFQR Program are required to
report the COVID–19 Vaccination
Coverage Among HCP measure. We
further note that in our final rule
removing staff vaccination
requirements, we clarified that we were
aligning our approach with that for
other infectious diseases, specifically
influenza, and that we would encourage
ongoing COVID–19 vaccination through
our quality reporting and value-based
incentive programs (88 FR 38486).
We believe this measure continues to
align with our goals to promote wellness
and disease prevention. Under CMS’
Meaningful Measures Framework 2.0,
the COVID–19 Vaccination Coverage
Among HCP measure addresses the
quality priorities of ‘‘Immunizations’’
and ‘‘Public Health’’ through the
Meaningful Measures Area of ‘‘Wellness
and Prevention.’’ Under the National
Quality Strategy, the measure addresses
the goal of ‘‘Safety’’ under the priority
area ‘‘Safety and Resiliency.’’ Our
response to COVID–19 is not fully
dependent on the emergency
declaration for the COVID–19 PHE and,
beyond the end of the COVID–19 PHE,
we continue to work to protect
individuals and communities from the
virus and its worst impacts by
supporting access to COVID–19
vaccines, treatments, and tests.
Comment: Many commenters did not
support updating the COVID–19
Vaccination Coverage Among HCP
measure because of concerns that the
frequency of changes to the CDC’s
definition of ‘‘up-to-date’’ combined
with the uncertainty around future
vaccination schedules creates
unnecessary burden for facilities. Some
of these commenters recommended
allowing voluntary reporting until the
appropriate definitions and guidance
are stable. One commenter stated that
understanding how changing guidelines
apply to all members of staff (such as
those with risk factors) is burdensome.
Others stated that publicly reporting
these data may not be meaningful to
consumers due to the changing
definitions and the time lag between
collection and public reporting.
Response: Since the adoption of the
current version of the measure, the
public health response to COVID–19 has
necessarily adapted to respond to the
changing nature of the virus’s
transmission and community spread.
When we finalized the adoption of the
COVID–19 Vaccination Coverage
Among HCP measure in the FY 2022 IPF
PPS final rule (86 FR 42640), we
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received several comments encouraging
us to continue to update the measure as
new evidence on COVID–19 continues
to arise and we stated our intention to
continue to work with partners
including FDA and CDC to consider any
updates to the measure in future
rulemaking as appropriate. We believe
that the measure modification aligns
with the CDC’s responsive approach to
COVID–19 and will continue to support
vaccination as the most effective means
to prevent the worst consequences of
COVID–19, including severe illness,
hospitalization, and death. We agree
with commenters who observe that
there is a delay between data collection
and public reporting for this measure
and note that such a delay exists for all
measures in the IPFQR Program.
However, we believe that the data will
provide meaningful information to
consumers in making healthcare
decisions because the data will be able
to reflect differences between IPFs in
COVID–19 vaccination coverage among
HCP even if the data do not reflect
immediate vaccination rates.
Comment: Many commenters
recommended that CMS reduce the
mandatory reporting frequency to
quarterly or to annually to reduce
reporting burden for facilities. Some of
these commenters stated that this
mirrors the reporting schedule for the
Influenza Vaccination Coverage Among
HCP measure which is in some quality
reporting programs.
Response: As we stated in the FY
2024 IPF PPS proposed rule (88 FR
21292), the measure developer noted
that the model used for this measure is
based on the Influenza Vaccination
Coverage Among HCP measure (CBE
#0431), and it intends to utilize a
similar approach to the modified
COVID–19 Vaccination Coverage
Among HCP measure if vaccination
strategy becomes seasonal. We continue
to monitor COVID–19 as part of our
public health response and will
consider information we collect to
inform any potential action that may
address seasonality in future
rulemaking.
Comment: Some commenters
expressed concern that the COVID–19
Vaccination Coverage Among HCP
measure has not been endorsed by the
CBE.
Response: The current version of the
measure received CBE endorsement
(CBE #3636, ‘‘Quarterly Reporting of
COVID–19 Vaccination Coverage
Among Healthcare Personnel’’) on July
26, 2022. As we stated in the FY 2024
IPF PPS proposed rule (88 FR 21292
through 21293), in the case of a
specified area or medical topic
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determined appropriate by the Secretary
for which a feasible and practical
measure has not been endorsed by the
entity with a contract under section
1890(a) of the Act, the Secretary may
specify a measure that is not so
endorsed as long as due consideration is
given to measures that have been
endorsed or adopted by a consensus
organization identified by the Secretary.
As discussed in section V.E.2.b. of the
proposed rule (88 FR 21292 through
21293) and this final rule, we reviewed
measures endorsed by consensus
organizations and were unable to
identify any other measures on this
topic endorsed by a consensus
organization; therefore, we believe the
exception for non- CBE- endorsed
measures applies. The measure steward,
CDC, is currently pursuing endorsement
for the modified version of the measure
as the current version of the measure
has already received endorsement.
Comment: Some commenters
recommended that CMS include an
exclusion for sincerely held religious
beliefs to adhere to HHS Office of Civil
Rights Guidance. Some of these
commenters also requested the measure
be updated to track the number of HCP
who decline vaccination. Several
commenters stated that there are many
factors beyond an IPF’s control (such as
weather, holidays, vaccine supply, etc.)
that may affect performance on this
measure.
Response: We recognize that there are
many reasons, including religious
objections or concerns regarding an
individual HCP’s specific health status
which may lead individual HCP to
decline vaccination. The CDC’s NHSN
tool allows facilities to report on the
number of HCP who were offered a
vaccination but declined for religious or
philosophical objections.244 We
understand the commenters’ concern
that there are many factors outside of an
IPF’s control that could affect
vaccination coverage; however, we
believe that all IPFs face such concerns
and that public reporting of these data
can help patients and their caregivers
identify which IPFs have better
vaccination coverage among their HCP.
Furthermore, we believe that reporting
of the measure based on one week per
month over three months will allow
some seasonal or other effects to be
mitigated. We wish to emphasize that
neither the modified measure nor the
current version of the measure mandate
vaccines. The COVID–19 Vaccination
244 https://www.cdc.gov/nhsn/forms/
COVIDVax.HCP_.FORM_May2022-508.pdf.
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Coverage Among HCP measure only
requires reporting of vaccination rates
for successful program participation.
Final Decision: After consideration of
the public comments we received, we
are finalizing modification of the
COVID–19 Vaccination Coverage
Among HCP measure as proposed.
F. Removal or Retention of IPFQR
Program Measures
1. Background
In the FY 2018 IPPS/LTCH PPS final
rule (82 FR 38463 through 38465) and
FY 2019 IPF PPS final rule (83 FR 38591
through 38593), we adopted several
considerations for removing or retaining
measures within the IPFQR Program.
Specifically, we have adopted eight
factors that we consider when
evaluating whether to propose a
measure for removal from the IPFQR
Program. These factors are: (1) measure
performance among IPFs is so high and
unvarying that meaningful distinctions
and improvements in performance can
no longer be made (‘‘topped out’’
measures); (2) measure does not align
with current clinical guidelines or
practice; (3) measure can be replaced by
a more broadly applicable measure
(across setting or populations) or a
measure that is more proximal in time
to desired patient outcomes for the
particular topic; (4) measure
performance or improvement does not
result in better patient outcomes; (5)
measure can be replaced by a measure
more strongly associated with desired
patient outcomes for the particular
topic; (6) measure collection or public
reporting leads to negative intended
consequences other than patient harm;
(7) measure is not feasible to implement
as specified; and (8) the costs associated
with a measure outweigh the benefit of
its continued use in the program. For
measure removal factor one, we
specified that a measure is ‘‘topped out’’
if it meets the following criteria: (1)
statistically indistinguishable
performance at the 75th and 90th
percentiles; and (2) the truncated
coefficient of variation is less than or
equal to 0.10.
We also adopted three factors for
consideration in determining whether to
retain a measure in the IPFQR Program,
even if the measure meets one or more
factors for removal. These retention
factors are: (1) measure aligns with other
CMS and HHS policy goals, such as
those delineated in the National Quality
Strategy and CMS Quality Strategy; (2)
measure aligns with other CMS
programs, including other quality
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reporting programs; and (3) measure
supports efforts to move IPFs towards
reporting electronic measures. In the FY
2018 IPPS/LTCH PPS final rule (82 FR
38464), we stated that these removal
and retention factors are considerations
that we consider in balancing the
benefits and drawbacks of removing or
retaining measures on a case-by-case
basis.
Since adoption, we have not proposed
any changes to these policies for
removal or retention and refer readers to
the FY 2018 IPPS/LTCH PPS final rule
(82 FR 38463 through 38465) and the FY
2019 IPF PPS final rule (83 FR 38591
through 38593) for more information.
We did not propose any updates to
these measure retention and removal
policies. We proposed to codify these
previously adopted policies at
§ 412.433(e).
We welcomed comments on this
proposal.
Comment: One commenter
recommended an additional factor,
relevance and importance of the
measure to patients, for CMS to consider
when deciding whether to remove or
modify a measure in the IPFQR. The
commenter stated this was consistent
with TEPs which inform the measure
development process and would
improve the patient centeredness of the
program.
Response: We appreciate this
recommendation and will consider it in
the future as we continue to evaluate all
elements of the IPFQR Program.
Final Decision: After consideration of
the public comments we received, we
are finalizing codification of our
measure retention and removal policies
as proposed.
2. Measures for Removal
We continue to evaluate our measure
set against these removal and retention
factors on an ongoing basis. In this
continual evaluation of the IPFQR
Program measure set under our
Meaningful Measures Framework and
according to our measure removal and
retention factors, we identified two
measures that we believe are
appropriate to remove from the IPFQR
Program beginning with the FY 2025
payment determination. Our discussion
of these measures follows.
a. Removal of the Patients Discharged
on Multiple Antipsychotic Medications
With Appropriate Justification (HBIPS–
5) (Previously Endorsed Under CBE
#0560) Measure Beginning With FY
2025 Payment Determination
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As we assessed our existing measure
set to ensure that it remains appropriate
for the IPFQR Program, we determined
that measure removal factor two (that is,
measure does not align with current
clinical guidelines or practice) applies
to the Patients Discharged on Multiple
Antipsychotic Medications with
Appropriate Justification (HBIPS–5)
(CBE #560) measure due to the
American Psychiatric Association’s
(APA’s) updated guidelines for patients
with schizophrenia.
We adopted the HBIPS–5 measure in
the FY 2013 IPPS/LTCH PPS final rule
as part of a set with the Patients
Discharged on Multiple Antipsychotic
Medications (HBIPS–4) (previously
endorsed under CBE #0552) measure
because of the belief that these two
measures would help reduce
unnecessary use of multiple
antipsychotics, which would lead to
better clinical outcomes and reduced
side effects for patients (77 FR 53649
through 53650). We subsequently
removed the HBIPS–4 measure in the
FY 2016 IPF PPS final rule (80 FR 46695
through 46696). As we described in that
final rule, following our adoption of
these measures, some experts, including
the CBE, provided input that the
HBIPS–4 measure did not provide
meaningful information about the
quality of care received by IPF patients.
This led to the removal of the HBIPS–
4 measure’s CBE endorsement in
January 2014. During the CBE’s review
of the HBIPS–4 measure in 2014, the
CBE observed that the HBIPS–4 and
HBIPS–5 measures could be collected
and reported separately and expressed
that the HBIPS–5 measure should be
retained in the IPFQR Program as it
continued to provide meaningful quality
of care information (80 FR 046695
through 46696).
Evidence supporting development
and adoption of the HBIPS–5 measure
included the APA Workgroup on
Schizophrenia’s 2004 Practice Guideline
for the Treatment of Patients with
Schizophrenia. These guidelines stated
that the ‘‘combinations of antipsychotics
. . . should be justified by strong
documentation that the patient is not
equally benefited by monotherapy.’’ 245
In December 2019, the APA Board of
Trustees approved updated guidelines
for treatment of patients with
schizophrenia.246 The updated
guidelines are based on evolving
clinical knowledge and have increased
245 https://www.researchgate.net/publication/
298561608_Practice_guideline_for_the_treatment_
of_patients_with_schizophrenia_second_edition.
246 https://ajp.psychiatryonline.org/doi/10.1176/
appi.ajp.2020.177901.
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focus and specificity of
recommendations for the use of
pharmacotherapy; they also underscore
the importance of patient preference
and shared-decision making.247 These
guidelines no longer contain the
recommendation that combinations of
antipsychotics should be justified by
strong documentation that patients are
not equally benefited by monotherapy.
Therefore, the guidelines that originally
supported the HBIPS–5 measure have
changed substantially, and the HBIPS–
5 measure is no longer aligned with
current clinical guidelines and practice.
Furthermore, the HBIPS–5 measure is
no longer supported by the measure
steward (that is, The Joint Commission),
who withdrew it from the CBE
endorsement process in 2019. As a
result, the HBIPS–5 measure lost its CBE
endorsement in October 2019.248
Subsequent to this, the CBE-convened
MAP’s discussion of measure set
removal for 2021–2022 included a
discussion of this measure. Because the
HBIPS–5 measure no longer aligns with
clinical guidelines and is no longer CBE
endorsed due to lack of support from
the measure developer, the MAP
recommended that the measure should
be removed from the IPFQR Program.249
We agree with the MAP’s assessment
that the measure no longer aligns with
clinical guidelines and therefore
proposed to remove the measure from
the IPFQR Program beginning with the
FY 2025 payment determination. We
note that data for the FY 2024 payment
determination represents care provided
in CY 2022 and will be reported to CMS
prior to the publication of this FY 2024
IPF PPS final rule; therefore, the FY
2025 payment determination is the first
period for which we can remove this
measure.
We invited comments on our
proposal.
Comment: Many commenters
supported removing HBIPS–5 from the
IPFQR Program. These commenters
agreed that the measure no longer aligns
with the updated clinical guidance from
the APA.
247 The American Psychiatric Association.
Practice Guideline for the Treatment of Patients
with Schizophrenia, Third Edition. Available at:
https://psychiatryonline.org/doi/book/10.1176/
appi.books.9780890424841. Accessed on February
15, 2023.
248 CMS Measures Inventory Tool. Patients
Discharged on multiple antipsychotic medications
with appropriate justification. Available at: https://
cmit.cms.gov/cmit/#/
MeasureView?variantId=1141§ionNumber=1.
249 MAP 2021–2022 Considerations for
Implementing Measures in Federal Programs.
Available at: https://mmshub.cms.gov/sites/default/
files/map_2021-2022_considerations_for_
implementing_measures_in_federal_programs_
final_report.pdf.
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Response: We thank these
commenters for their support.
Comment: Several commenters
expressed concern about the long-term
effects of psychotropic medications,
especially antipsychotics, and
recommended that CMS defer removal
until additional research can be
performed to ensure there are minimal
long-term effects of antipsychotic
medications.
Response: We appreciate commenters’
concern about the long-term effects of
psychotropic medications. We note that
our proposed removal of the measure
was based on the updated APA
guidelines for treatment of patients with
schizophrenia. These guidelines
underwent a rigorous review process
prior to being updated, which included
a review of the benefits and harms of
each treatment.250
Final Decision: After consideration of
the public comments we received, we
are finalizing removal of the Patients
Discharged on Multiple Antipsychotic
Medications with Appropriate
Justification (HBIPS–5) measure as
proposed.
b. Removal of the Tobacco Use Brief
Intervention Provided or Offered and
Tobacco Use Brief Intervention (TOB–2/
2a) Measure Beginning With the FY
2025 Payment Determination
We adopted the Tobacco Use Brief
Intervention Provided or Offered and
Tobacco Use Brief Intervention (TOB–2/
2a) measure in the FY 2015 IPF PPS
final rule (79 FR 45971 through 45972)
because of our belief that it is important
to address the common comorbidity of
tobacco use among IPF patients. The
TOB–2/2a measure requires IPFs to
chart-abstract measure data on a sample
of IPF patient records, in accordance
with established sampling policies (80
FR 46717 through 46719). When we
introduced the TOB–2/2a measure to
the IPFQR Program, the benefits of this
measure were high because IPF
performance was not consistent with
respect to, and there were no other
measures addressing, provision of
tobacco use cessation counseling or
treatment. At the time, the TOB–2/2a
measure provided a means of
distinguishing IPF performance
regarding, and incentivized facilities to
improve rates of, treatment for this
common comorbidity. To further
address tobacco use, we subsequently
adopted the Tobacco Use Treatment
Provided or Offered at Discharge and
250 https://www.psychiatry.org/File%20Library/
Psychiatrists/Practice/
Clinical%20Practice%20Guidelines/GuidelineDevelopment-Process.pdf.
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Tobacco Use Treatment at Discharge
(TOB–3/3a) measure in the FY 2016 IPF
PPS final rule (80 FR 46696 through
46699).
In the FY 2022 IPF PPS proposed rule,
we proposed to remove the Tobacco Use
Brief Intervention Provided or Offered
and Tobacco Use Brief Intervention
(TOB–2/2a) measure from the IPFQR
Program beginning with the FY 2024
payment determination under our
measure removal factor 8, the costs
associated with a measure outweigh the
benefit of its continued use in the
program (86 FR 19508 through 19509).
We expressed our belief that the quality
improvement benefits from the TOB–2/
2a measure had greatly diminished
because performance had leveled off,
that is overall performance on the
measure was no longer improving. We
took this to mean that most IPFs
routinely offer tobacco use brief
interventions.
In the FY 2022 IPF PPS proposed rule,
we also expressed our belief that the
costs of maintaining this measure are
high because costs are multi-faceted and
include not only the IPFs’ burden
associated with reporting, but also our
costs associated with implementing and
maintaining the measure (86 FR 19508
through 19509). Additionally, we must
expend resources in maintaining
information collection systems,
analyzing reported data, and providing
public reporting of the collected
information. We expressed that, for this
measure, IPF information collection
burden and related costs associated with
reporting this measure to CMS were
high because the measure is a chartabstracted measure. Furthermore, we
observed CMS incurs costs associated
with the program oversight of the
measure for public display.
However, in the FY 2022 IPF PPS
final rule, we did not finalize our
proposal to remove the Tobacco Use
Brief Intervention Provided or Offered
and Tobacco Use Brief Intervention
(TOB–2/2a) measure (86 FR 42648
through 42651). We stated that,
following review of the public
comments we received, we believed the
benefits of continuing to encourage
facilities to offer tobacco use brief
interventions were greater than we had
estimated. We noted that these benefits
included the potential for IPFs to
continue improving performance on the
TOB–2/2a measure, the importance of
tobacco use interventions due to
increased tobacco use during the
COVID–19 pandemic, and this
measure’s potential influence on other
quality improvement activities related
to tobacco use.
In our continual evaluation of the
IPFQR Program measure set under our
Meaningful Measures Framework and
according to our measure removal and
retention factors, we observed that
having two measures addressing tobacco
use, which are both associated with
relatively high information collection
burden, may not appropriately balance
costs and benefits within the program.
While we believe that both the TOB–2/
2a measure and the TOB–3/3a measure
address clinically important
interventions to address smoking in this
population, we believe that the overall
cost associated with retaining both of
these measures outweighs the benefit of
having two measures to address
treatment for the same comorbidity
among the same patient population.
Both measures capture information
about tobacco cessation counseling and
FDA-approved tobacco cessation
medications. The difference between the
measures is that the TOB–2/2a measure
captures whether the tobacco cessation
counseling and FDA-approved tobacco
cessation medications were offered or
refused during the inpatient stay, while
the TOB–3/3a measure captures
whether a referral to outpatient tobacco
cessation counseling and FDA-approved
tobacco cessation medications were
offered or refused at the time of the
patient’s discharge.
As we considered each of these
measures, we determined that it would
be more appropriate to retain the TOB–
3/3a measure in the IPFQR Program,
that is, to remove the TOB–2/2a
measure instead of the TOB–3/3a
measure, because there is more
opportunity for improvement on the
TOB–3/3a measure. Specifically, the
performance on the TOB–3/3a measure
is lower than performance on the TOB–
2/2a measure. National performance on
TOB–2 and 2a measure and TOB–3 and
3a measure for the last five payment
determination years in the IPFQR
Program is presented in Table 19. Given
the relatively high performance on the
TOB–2/2a measure compared to the
TOB–3/3a measure, we believe that
retaining the TOB–3/3a measure, and
removing the TOB–2/2a measure, would
provide more opportunity to drive
improvement among IPFs; therefore,
would potentially impact more patients.
As described earlier in this section
VI.F.2.b of this final rule, because the
TOB–2/2a measure has a high cost
(especially due to its high information
collection burden), we believe that these
high costs are no longer greater than the
benefits of retaining this measure.
Therefore, we believe measure removal
factor 8 (that is, the costs associated
with a measure outweigh the benefit of
its continued use in the IPFQR
Program), applies to the TOB–2/2a
measure.
Furthermore, the TOB–2/2a measure
is no longer supported by the measure
steward (that is, The Joint Commission),
who withdrew it from the CBE
endorsement process in 2018. Therefore,
the TOB–2/2a measure has not been
CBE endorsed since October 2018.251
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251 CMS Measures Inventory Tool. Tobacco Use
Treatment Provided or Offered. Available at:
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Subsequent to this, the CBE-convened
MAP’s discussion of measure set
removal for 2021and 2022 included a
discussion of this measure. Because the
TOB–2/2a measure is a high-cost
measure and is no longer CBE endorsed,
the MAP recommended that we remove
the measure from the IPFQR Program.252
We agree with the MAP that this is a
high-cost measure. Furthermore, we
recognize that it is similar to the other
tobacco use measure in the IPFQR
Program measure set (that is, the TOB–
3/3a measure) which we did not
propose to remove. Therefore, we
proposed to remove Tobacco Use Brief
Intervention Provided or Offered and
Tobacco Use Brief Intervention (TOB–2/
2a) measure under our measure removal
factor 8, ‘‘the costs associated with a
measure outweigh the benefit of its
continued use in the program,’’
beginning with FY 2025 payment
determination. We note that data for the
FY 2024 payment determination
represents care provided in CY 2022
and will be reported to CMS prior to the
publication of this FY 2024 IPF PPS
final rule; therefore, the FY 2025
payment determination is the first
period for which we can remove this
measure.
We invited public comment on this
proposal.
Comment: Many commenters
supported removal of the TOB–2/2a
measure because it will reduce burden
with minimal impact on patient
outcomes due to the retention of the
TOB–3/3a measure. Some of these
commenters stated that the TOB–3/3a
measure has more room for
improvement and is more likely to lead
to improved patient outcomes.
Response: We thank these
commenters for their support.
Comment: Many commenters opposed
removal of the TOB–2/2a measure.
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MeasureView?variantId=1818§ionNumber=1.
252 MAP 2021–2022 Considerations for
Implementing Measures in Federal Programs.
Available at: https://mmshub.cms.gov/sites/default/
files/map_2021-2022_considerations_for_
implementing_measures_in_federal_programs_
final_report.pdf.
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These commenters stated that tobacco
use is a common comorbidity among
this patient population that leads to
negative long-term health outcomes.
These commenters expressed that the
TOB–2/2a and TOB–3/3a measures both
address important interventions to
reduce tobacco use and therefore
recommended retaining both measures.
Some of these commenters expressed
concern that, without the TOB–2/2a
measure, IPFs will not offer tobacco use
interventions in the inpatient setting
which represents a missed opportunity
to increase the likelihood that these
patients will quit using tobacco. Some
of these commenters stated that there is
still room for improvement on the TOB–
2/2a measure.
Response: We agree with commenters
that tobacco use is a common
comorbidity among this patient
population that leads to negative longterm health outcomes. We remain
committed to the screening, counseling
and provision of smoking intervention
services in this population of patients.
We note that studies have demonstrated
that during the acute hospital stay, there
is no statistically significant increase in
smoking cessation for non-intensive
counseling interventions, such as brief
intervention,253 which is what TOB–2/
2a measures. We will retain TOB–3/3a
which focuses on the provision of
smoking cessation referral and treatment
for smoking cessation at discharge, to be
continued in the ambulatory setting,
which studies have shown a greater
benefit to the patient. Even though we
are finalizing the removal of the TOB–
2/2a measure, and therefore IPFs and
IPFs will no longer be required to
collect and submit TOB–2/2a data to
CMS, IPFs are still encouraged to
continue to provide smoking cessation
counseling and brief interventions
during the psychiatric stay as
determined appropriate by the patient’s
253 : Rigotti NA, Clair C, Munafo
` MR, Stead LF.
Interventions for smoking cessation in hospitalised
patients. Cochrane Database Syst Rev. 2012 May
16;5(5):CD001837. doi: 10.1002/
14651858.CD001837.pub3. PMID: 22592676;
PMCID: PMC4498489. Available at:: https://
www.ncbi.nlm.nih.gov/pmc/articles/PMC4498489/.
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provider and patient. We appreciate
commenters concerns and will continue
to monitor whether additional measures
related to smoking cessation and/or
intensive behavioral counseling are
necessary. We also support the
extensive other work that is being done
by HHS and the broader Administration
to reduce smoking, including the
framework proposed by the Office of the
Assistant Secretary for Health (OASH)
(88 FR 42377).
We agree with commenters that TOB–
2/2a and TOB–3/3a both address
important interventions (that is, tobacco
use treatment brief intervention
provided or offered during the inpatient
stay and tobacco use treatment provided
or offered at discharge) and that there is
still room for improvement for both
measures. While it is possible that,
without the TOB–2/2a measure, some
IPFs may stop providing inpatient
tobacco use interventions prior to
during the patient’s discharge planning,
we continue to believe that the benefit
of having two measures to address this
comorbidity does not outweigh the
significant reporting burden for IPF’s
associated with these specific measures.
We note that we believe that the benefits
of tobacco use interventions during the
inpatient stay are high; however, we do
not believe the benefits of measuring
these interventions along with similar
interventions at discharge are
sufficiently high to outweigh the
burden.
Final Decision: After consideration of
the public comments we received, we
are finalizing removal of the Tobacco
Use Brief Intervention Provided or
Offered and Tobacco Use Brief
Intervention measure as proposed.
G. Summary of IPFQR Program
Measures
1. IPFQR Program Measures for the FY
2024 Payment Determination
We did not propose any changes to
our measure set for the FY 2024
payment determination. The 14
measures which will be in the program
for FY 2024 payment determination are
shown in Table 20.
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In this final rule. we are removing two
measures for the FY 2025 payment
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determination and subsequent years. We
also are modifying one measure for the
FY 2025 payment determination and
subsequent years. The 12 measures,
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which will be in the program for FY
2025 payment determination are shown
Table 21.
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2. IPFQR Program Measures for the FY
2025 Payment Determination
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3. IPFQR Program Measures for the FY
2026 Payment Determination
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The measure set for FY 2026 payment
determination and subsequent years
will include 13 mandatory and two
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voluntary measures. This includes the
12 mandatory measures listed in Table
21 of this final rule for the FY 2025
payment determination and subsequent
years, as well as the one mandatory
measure and two voluntary measures
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we adopted for the FY 2026 payment
determination and subsequent years.
The measures which will be in the
program for FY 2026 payment
determination are shown Table 22.
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The measure set for the FY 2027
payment determination and subsequent
years, will include 15 mandatory
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measures and one voluntary measure.
This includes the 13 mandatory
measures listed in Table 22 of this final
rule for the FY 2026 payment
determination and subsequent years, as
well as the two measures which we are
requiring for the FY 2027 payment
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determination and subsequent years. It
also includes the one new voluntary
measure adopted in section VI.D.5 of
this final rule. The measures which we
are finalizing for the FY 2027 payment
determination and subsequent years are
shown Table 23.
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4. IPFQR Program Measures for the FY
2027 IPFQR Program’s Payment
Determination
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5. IPFQR Program Measures for the FY
2028 Payment Determination
The measure set for the FY 2028
payment determination and subsequent
years will include 16 mandatory
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measures. This includes the 15
mandatory measures listed in Table 23
of this final rule for the FY 2027
payment determination as well as the
measure which we finalized beginning
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with the FY 2028 payment
determination. The measures which will
be in the program beginning with the FY
2028 payment determination are shown
Table 24.
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H. Public Display and Review
Requirements
In the FY 2013 IPPS/LTCH PPS final
rule (77 FR 53653 through 53654), we
adopted procedures for making data
submitted under the IPFQR Program
available to the public, after an IPF has
the opportunity to review such data
prior to public display, as required by
section 1886(s)(4)(E) of the Act. We
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adopted modifications to these
procedural requirements in the FY 2014
IPPS/LTCH PPS final rule (78 FR 50897
through 50898), and the FY 2017 IPPS/
LTCH PPS final rule (81 FR 57248
through 57249).
Specifically, the IPFQR Program
adopted a policy to provide IPFs a 30day period to review their data, and
submit corrections to errors resulting
from CMS calculations, prior to public
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51141
display on a CMS website. The IPFQR
Program notifies IPFs of the exact
timeframes for this preview period and
public display through subregulatory
guidance. We did not propose any
changes to these requirements.
We proposed to codify the procedural
requirements for public reporting of
IPFQR Program data at § 412.433(g). If
finalized, paragraph (g) would provide
that IPFs will have a period of 30 days
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to review data on quality measures that
CMS received under the IPFQR
Program, and submit corrections to
errors resulting from CMS calculations,
prior to CMS publishing this data on a
CMS website.
We welcomed comments on our
proposal to codify these policies.
We did not receive any comments on
this proposal.
Final Decision: We are finalizing
codification of these policies.
I. Form, Manner, and Timing of Quality
Data Submission for the FY 2024
Payment Determination and Subsequent
Years
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1. Procedural Requirements for the FY
2024 Payment Determination and
Subsequent Years
We refer readers to the FY 2013 IPPS/
LTCH PPS final rule (77 FR 53654
through 53655), the FY 2014 IPPS/LTCH
PPS final rule (78 FR 50898 through
50899), the FY 2018 IPPS/LTCH PPS
final rule (82 FR 38471 through 38472),
and the FY 2022 IPF PPS final rule (86
FR 42656 through 42657) for our
previously finalized procedural
requirements for participation in, and
withdrawal from, the IPFQR Program, as
well as data submission requirements.
We did not propose any changes to our
previously finalized procedural
requirements.
We proposed to codify these
procedural requirements for
participation in the IPFQR Program at
§ 412.433(b) through (d). Paragraphs (b)
through (d) will set forth the procedural
requirements for an IPF to register for,
or withdraw from, participation in the
IPFQR Program and to submit the
required data on measures in a form and
manner and time specified by CMS.
We welcomed comments on our
proposal to codify these policies.
We did not receive any comments on
this proposal.
Final Decision: We are finalizing
codification of the procedural
requirements for participation in the
IPFQR Program at § 412.433(b) through
(d). We are finalizing the regulation text
as proposed except to replace references
to ‘‘QualityNet’’ with ‘‘CMS-designated
information system’’ and update the
description of the registration process
because we inadvertently referred to
QualityNet in the proposed rule. We
have migrated to a new internet system
for many quality reporting programs,
and we use the term ‘‘CMS-designated
information system’’ to refer both to that
system and any future updates to it.
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2. Data Submission Requirements for
the FY 2025 Payment Determination
and Subsequent Years
4. Data Submission Requirements for
the FY 2027 Payment Determination
and Subsequent Years
We refer readers to the FY 2013 IPPS/
LTCH PPS final rule (77 FR 53655
through 53657), the FY 2014 IPPS/LTCH
PPS final rule (78 FR 50899 through
50900), the FY 2018 IPPS/LTCH PPS
final rule (82 FR 38472 through 38473),
and the FY 2022 IPF PPS final rule (86
FR 42657 through 42661) for our
previously finalized data submission
requirements.
The measure we are modifying
beginning with the FY 2025 payment
determination—the COVID–19
Vaccination Coverage Among HCP
measure—requires facilities to report
data on the number of HCP who have
received a complete vaccination course
of a COVID–19 vaccine through the
Centers for Disease Control and
Prevention’s (CDC’s) National
Healthcare Safety Network (NHSN). We
are updating this measure to no longer
refer to ‘‘complete vaccination course’’
but instead to refer to ‘‘up-to-date’’
vaccination, as described in section
VI.E. of this final rule.
We did not propose any updates to
the form, manner, and timing of data
submission for the COVID–19
Vaccination Coverage Among HCP
measure and refer readers to the FY
2022 IPF PPS final rule (86 FR 42657)
for these policies.
In section VI.D.5. of this final rule, we
are adopting one patient-reported
measure, Psychiatric Inpatient
Experience (PIX) measure for voluntary
reporting beginning with the CY 2025
performance period (the data for which
will be submitted to CMS during CY
2026) and mandatory reporting
beginning with the FY 2028 payment
determination (that is, data from the CY
2026 performance period submitted to
CMS during CY 2027). Because, unlike
other patient experience of care
measures, this measure is collected by
facilities prior to discharge, we
proposed that facilities would report
these data using the patient-level data
reporting described in the FY 2022 IPF
PPS final rule (86 FR 42658 through
42661).
We invited public comment on our
proposal.
We did not receive any public
comments on this proposal.
Final Decision: We are finalizing our
proposal for data submission
requirements for the FY 2027 payment
determination and subsequent years. We
note that reporting these data will be
voluntary for the FY 2027 payment
determination and will be mandatory
beginning with the FY 2028 payment
determination.
3. Data Submission Requirements for
the FY 2026 Payment Determination
and Subsequent Years
In sections VI.D 3 and VI.D.4 of this
final rule, we are adopting measures for
voluntary reporting for the FY 2026
IPFQR Program and mandatory
reporting for the FY 2027 IPFQR
Program’s payment determination and
subsequent years. These measures are
the Screening for Social Drivers of
Health measure and Screen Positive
Rate for Social Drivers of Health
measure. We proposed that our
previously finalized data submission
requirements, specifically, our
previously finalized data submission
requirements for aggregate data
reporting described in the FY 2018
IPPS/LTCH PPS final rule (82 FR 38472
through 38473) would apply to these
measures.
We invited public comment on our
proposal.
We did not receive any public
comments on this proposal.
Final Decision: We are finalizing our
proposal for data submission
requirements for the FY 2026 payment
determination and subsequent years.
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5. Data Validation Pilot Beginning With
Data Submitted in CY 2025
As discussed in the FY 2019 IPF PPS
final rule (83 FR 28607) and in the FY
2022 IPF PPS final rule (86 FR 42661),
we are concerned that the ability to
detect error is lower for aggregate
measure data reporting than for patientlevel data reporting (that is, data
regarding each patient included in a
measure and, for example, whether the
patient was included in the numerator
and denominator of the measure). In the
FY 2022 IPF PPS final rule, we noted
that adoption of patient-level data
requirements would enable us to adopt
a data validation policy for the IPFQR
Program in the future (86 FR 42661). We
believe that it would be appropriate to
develop such a policy incrementally
through adoption of a data validation
pilot prior to national implementation
of data validation within the IPFQR
Program. We sought public input on a
potential data validation pilot, and
many commenters supported the
concept of data validation following
implementation of patient-level
reporting (86 FR 42661). In the FY 2022
IPF PPS final rule, we adopted
mandatory patient-level reporting
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beginning with data submitted in CY
2023 affecting the FY 2024 payment
determination and reflecting care
provided during CY 2022 (86 FR 42658
through 42661).
We are now finalizing a data
validation pilot beginning with data
submitted in CY 2025 (reflecting care
provided during CY 2024). When we
sought public comment on a data
validation pilot in the FY 2022 IPF PPS
proposed rule (86 FR 19515), we
requested input on potential elements of
such a pilot, including the number of
measures and the number of
participating IPFs. As summarized in
the FY 2022 IPF PPS final rule (86 FR
42661), one commenter recommended
selecting two measures and 200 IPFs for
this pilot. We considered that
recommendation; however, to align with
validation policies in our other quality
reporting programs, we decided to
request a specific number of charts.
Specifically, we proposed to request
eight charts per quarter from each IPF as
opposed to requesting all of the charts
that each facility used to calculate one
or more specific measures. We also
decided to initiate our pilot with fewer
IPFs than the commenter recommended
to limit the burden associated with this
pilot.
We also reviewed the validation
policies of other quality reporting
programs. We specifically reviewed the
Hospital IQR Program’s chart-abstracted
measure validation policies described in
the FY 2017 IPPS/LTCH PPS final rule
(81 FR 57179 through 57180), the
Hospital IQR Program’s pilot for eCQM
validation described in the FY 2015
IPPS/LTCH PPS final rule (79 FR 50262
through 50273), the Hospital Outpatient
Quality Reporting (OQR) Program’s
planned pilot of data validation as
described in the CY 2009 OPPS/ASC
final rule (73 FR 68502), and the
Hospital OQR Program’s finalized
validation policies as described in the
CY 2012 OPPS/ASC final rule (76 FR
74485) and the CY 2018 OPPS/ASC
final rule (82 FR 59441 through 5944)
because these programs are also pay-forreporting programs, like the IPFQR
Program.
Following our review of the
validation policies within these
programs, we proposed a validation
pilot in which we would randomly
select on an annual basis up to 100 IPFs
and request each selected IPF to provide
to CMS eight charts per quarter, a total
of 32 charts per year, used to calculate
all chart-based measures beginning with
data submitted in CY 2025. We believe
that randomly selecting up to 100 IPFs
would provide a sufficiently large set of
IPFs to meaningfully test our validation
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procedures while minimizing burden
for IPFs. We will specify the timeline
and mechanism for submitting data in
our data requests to individual IPFs that
have been selected to participate in the
validation pilot. We note that consistent
with the Hospital IQR Program, we will
reimburse IPFs for the cost of submitting
charts for validation at a rate of $3.00
per chart (85 FR 58949).
Because this is a voluntary pilot, we
recognize that some selected IPFs will
not participate; however, we believe
that this pilot would be beneficial for
IPFs that do participate as an
opportunity to receive education and
feedback on the data they submit prior
to future proposal and adoption of a
validation requirement in the IPFQR
Program.
We invited comments on our
proposal.
Comment: Several commenters
expressed support for the data
validation pilot.
Response: We thank these
commenters for their support.
Comment: Several commenters
provided recommendations for the data
validation pilot. One commenter
suggested allowing participants to opt
into the pilot as opposed to selecting
potential participants. One commenter
requested that CMS ensure that the
individuals doing the data validation
have clinical expertise in the psychiatric
setting to ensure appropriate
interpretation of data. Another
commenter recommended that CMS
complete the pilot and analyze the data
generated by the pilot prior to proposing
and adopting a full data validation
program.
Response: We thank these
commenters for their input. We note
that the data validation pilot described
in this section is based on validation
programs in other quality reporting
programs. We believe that selecting IPFs
to participate will allow us to test our
processes for selection and notification
and therefore we believe that this will
be a more effective test than allowing
IPFs to opt into the pilot. We note that
participation in the data validation pilot
will be voluntary for the IPFs which we
select. We will consider
recommendations for qualifications for
personnel to perform the data validation
and for analysis of the results as we
implement this program. We believe it
is appropriate to develop a data
validation policy incrementally through
adoption of a data validation pilot prior
to national implementation of data
validation within the IPFQR Program.
We intend to analyze data collected
through this data validation pilot to
inform development of a future
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nationally implemented data validation
program. We note that while we will
analyze data collected through the data
validation pilot in developing the
program for national implementation,
the pilot will be ongoing until national
implementation so that we can continue
to collect data and IPFs can continue to
receive education and feedback on the
data they submit.
Comment: One commenter expressed
that a data validation pilot with
payment ramifications is premature
because patient-level data submission is
still new to the IPFQR Program, because
CMS has not sufficiently defined the
pilot elements, and because it is unclear
that there would be auditors with
sufficient clinical expertise. Another
commenter recommended that CMS use
the data in the future IPF patient
assessment instrument (PAI) to validate
quality measure data. Another
commenter recommended postponing
this pilot until the financial and staffing
shortages caused by the COVID–19
pandemic have been resolved.
Response: We note that the
participation in the data validation pilot
is voluntary, and that IPFs will not
receive any payment penalties during
the data validation program’s pilot
period. With respect to the future IPF
PAI, we will consider the potential
interplay between data elements
included in the PAI and IPFQR Program
quality measure data for validation
purposes, but believe those
considerations are premature as a PAI
has not yet been implemented for the
IPF setting. Finally, we recognize that
healthcare providers, including IPFs, are
still recovering from the effects of the
COVID–19 pandemic, but note that
participation in the data validation pilot
is voluntary.
Comment: One commenter stated that
the reimbursement rate of $3.00/chart is
insufficient to cover the time and
materials associated with participating
in the pilot.
Response: We understand the
commenters concern that $3.00/chart
may not cover the time and materials
associated with participating in the
pilot. We note that this reimbursement
is consistent with the reimbursement
rates for submitting charts for validation
in other quality reporting programs.
However, we intend to use the pilot
program to identify potential
modifications prior to adopting a full
validation program. We will consider
the appropriateness of our
reimbursement at that time.
Final Decision: After consideration of
the public comments we received, we
are finalizing our data validation pilot
as proposed.
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6. Quality Measure Sampling
Requirements
We refer readers to the FY 2013 IPPS/
LTCH PPS final rule (77 FR 53657
through 53658), the FY 2014 IPPS/LTCH
PPS final rule (78 FR 50901 through
50902), the FY 2016 IPF PPS final rule
(80 FR 46717 through 46719), and the
FY 2019 IPF PPS final rule (83 FR 38607
through 38608) for discussions of our
previously finalized sampling policies.
Because the Facility Commitment to
Health Equity measure proposed in
section VI.D.2 of this final rule is a
structural attestation measure, these
policies do not apply to that measure.
Additionally, because the Screening for
Social Drivers of Health measure
(described in section VI.D.3 of this final
rule) applies to all patients and the
Screen Positive Rate for Social Drivers
of Health measure (described in section
VI.D.4 of this final rule) applies to all
patients who have been screened for
health-related social needs (HRSNs), our
previously finalized sampling policies
would not apply to these two measures.
As described in the FY 2022 IPF PPS
final rule, our sampling policies do not
apply to the COVID–19 Vaccination
Coverage Among Healthcare Personnel
measure because the denominator is all
healthcare personnel (86 FR 42661).
Generally, we have applied our
sampling procedures to chart-abstracted
measures, where appropriate (that is,
where the measure does not require
application to the entire patient
population). However, because the PIX
survey measure is a patient reported
measure, we have considered whether
our sampling procedures for chartabstracted measures are appropriate for
this measure. After consideration of our
current sampling procedures and
sampling for patient reported measures
in other quality reporting programs
(specifically, the requirements for
reporting the HCAHPS measure), we
proposed that the PIX survey measure
(described in section VI.D.5 of this final
rule) would be eligible for sampling but
would not be included in the global
sample. Instead, we proposed that
sampling for this measure would align
with sampling for the HCAHPS survey
measure in acute care hospitals and the
Hospital IQR Program as described in
the HCAHPS Quality Assurance
Guidelines.254 Specifically, we
proposed to require IPFs to develop
sampling plans that ensure that IPFs are
able to submit data for 300 completed
PIX surveys per year. IPFs will be
254 HCHAPS Quality Assurance Guidelines,
Version 17.0. March 2022. Available at: https://
hcahpsonline.org/globalassets/hcahps/qualityassurance/2022_qag_v17.0.pdf.
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required to sample from every month
throughout the entire reporting period
and not stop sampling or curtail ongoing
interview activities once a certain
number of completed surveys has been
attained. IPFs that are unable to reach
300 completed surveys through
sampling will be required to submit data
on survey results for all eligible patient
discharges.
We invited public comment on our
proposal.
Comment: One commenter
recommended allowing facilities to
apply their sampling methodologies to
the Screening for Social Drivers of
Health measure and the Screen Positive
Rate for Social Drivers of Health
measure to reduce burden.
Response: We acknowledge that
applying sampling methodologies for
these two measures would impact
abstraction and reporting burden. We
have proposed these measures to align
with other quality reporting and valuebased purchasing programs
(specifically, the Hospital IQR Program)
as well as the same measure proposals
for the PPS-Exempt Cancer Hospital
Quality Reporting Program in the FY
2024 IPPS/LTCH PPS proposed rule (88
FR 27122 through 27130) and the EndStage Renal Disease (ESRD) Quality
Incentive Program in the CY 2024 ESRD
Prospective Payment System proposed
rule (88 FR 42509 through 42518). We
note that the Hospital IQR Program
adopted these two measures without
sampling in the FY 2023 IPPS/LTCH
PPS final rule (87 FR 49191 through
49220). We believe that adopting these
measures consistently across programs
will increase the cross-setting
comparability of measure results for the
Screening for Social Drivers of Health
measure; provide more information
regarding community needs for specific
communities that are served by multiple
healthcare organizations for the Screen
Positive Rate for Social Drivers of
Health measure; and ensure that we are
consistently conveying the importance
of identifying and addressing HRSNs
across all settings.
Comment: Several commenters
recommended that CMS establish a
statistically valid random sampling
process for all IPFs to apply for the PIX
survey measure to ensure that selection
bias does not occur.
Response: We will provide updated
guidance for developing sampling plans
and other implementation guidance for
the PIX survey measure. This guidance
will align with sampling guidance for
the HCAHPS measure in the Hospital
IQR Program.
Comment: One commenter requested
clarification regarding whether all
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patients would be eligible for inclusion
in the sample for the PIX survey
measure or only Medicare patients.
Response: To the extent feasible we
believe that it is important to include all
patients in our quality reporting
measures. While some measures do not
allow inclusion of all patients
(specifically, measures abstracted from
Medicare claims data); there are no
feasibility issues which require the PIX
survey measure to be limited to patients
covered by any specific payer.
Therefore, all patients, regardless of
payer, are included in the population
from which the sample for this measure
is selected.
Comment: One commenter requested
clarification regarding whether IPFs that
were unable to reach 300 completed
surveys would be penalized.
Response: IPFs that are unable to
reach 300 completed PIX surveys
because of the size or characteristics of
their patient population should submit
data on all eligible patients. IPFs that
meet this requirement would not be
penalized for not submitting data on 300
completed PIX surveys.
Final Decision: We are finalizing our
proposals related to sampling for the
newly adopted measures.
7. Non-Measure Data Collection
We refer readers to the FY 2015 IPF
PPS final rule (79 FR 45973), the FY
2016 IPF PPS final rule (80 FR 46717),
and the FY 2019 IPF PPS final rule (83
FR 38608) for our previously finalized
non-measure data collection policies.
We did not propose any changes to
these policies.
8. Data Accuracy and Completeness
Acknowledgement (DACA)
Requirements
We refer readers to the FY 2013 IPPS/
LTCH PPS final rule (77 FR 53658) for
our previously finalized DACA
requirements. We did not propose any
changes to these policies.
J. Reconsideration and Appeals
Procedures
We refer readers to 42 CFR 412.434
for the IPFQR Program’s reconsideration
and appeals procedures. We did not
propose any changes to these policies.
K. Extraordinary Circumstances
Exceptions (ECE) Policy
We refer readers to the FY 2013 IPPS/
LTCH PPS final rule (77 FR 53659
through 53660), the FY 2014 IPPS/LTCH
PPS final rule (78 FR 50903), the FY
2015 IPF PPS final rule (79 FR 45978),
and the FY 2018 IPPS/LTCH PPS final
rule (82 FR 38473 through 38474) for
our previously finalized Extraordinary
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remaining provisions are not associated
with any information collection
requirements. In that regard they are not
subject to the requirements of the PRA
and are not addressed under this section
of the preamble. For this rule’s full
burden implications, please see the
Regulatory Impact Analysis under
section VIII of this final rule.
VII. Collection of Information
Requirements
Under the Paperwork Reduction Act
of 1995 (PRA) (44 U.S.C. 3501 et seq.),
we are required to provide 30-day notice
in the Federal Register and solicit
public comment before a ‘‘collection of
information’’ requirement is submitted
to the Office of Management and Budget
(OMB) for review and approval. For the
purposes of the PRA and this section of
the preamble, collection of information
is defined under 5 CFR 1320.3(c) of the
PRA’s implementing regulations.
To fairly evaluate whether an
information collection should be
approved by OMB, section 3506(c)(2)(A)
of the PRA requires that we solicit
comment on the following issues:
• The need for the information
collection and its usefulness in carrying
out the proper functions of our agency.
• The accuracy of our estimate of the
information collection burden.
• The quality, utility, and clarity of
the information to be collected.
• Recommendations to minimize the
information collection burden on the
affected public, including automated
collection techniques.
Our April 10, 2023 (88 FR 21238)
proposed rule solicited public comment
on each of the aforementioned issues for
the following sections of the rule that
contained information collection
requirements beginning in CY 2024
through CY 2027. A summary of these
comments and our responses is in
section VII.C of this final rule. The
As indicated, we are adjusting our
hourly wage estimates by a factor of 100
percent. This is necessarily a rough
adjustment, both because fringe benefits
and other indirect costs vary
significantly from employer to
employer, and because methods of
estimating these costs vary widely from
study to study. Nonetheless, we believe
that doubling the hourly wage to
estimate the total cost is a reasonably
accurate estimation method.
In the FY 2022 IPF PPS final rule (86
FR 42662), which was the most recent
rule in which we adopted updates to the
IPFQR Program, we estimated that
reporting measures for the IPFQR
Program could be accomplished by a
Medical Records and Health
Information Technician (BLS
Occupation Code: 29–2072) with a
median hourly wage of $20.50/hour
(BLS, May 2019). We note that since the
publication of the FY 2022 IPF PPS final
rule, the BLS occupation category of
‘Medical Records and Health
Information Technician (BLS
Occupation Code: 29–2071)’ has been
replaced with ‘Medical Records
Specialist (BLS Occupation Code: 29–
2072). Therefore, in the FY 2024 IPF
PPS proposed rule, we proposed to
adjust our cost estimates using BLS’
May 2021 median wage rate figure of
$22.43/hour, an increase of $1.93/hour
($22.43/hour–$20.50/hour). When
factoring in our overhead and other
indirect cost adjustments, the wage is
increased by $3.86/hour ($44.86/hour–
$41.00/hour).
We have also estimated the average
hourly cost for patients undertaking
administrative and other tasks on their
own time. Based on recommendations
from the Valuing Time in U.S.
Department of Health and Human
Services Regulatory Impact Analyses 256
guidance we have estimated a post-tax
wage of $20.71/hr. The Valuing Time in
U.S. Department of Health and Human
Services Regulatory Impact Analyses:
Conceptual Framework and Best
Practices identifies the approach for
valuing time when individuals
undertake activities on their own time.
To derive the costs for patients, a
measurement of the usual weekly
earnings of wage and salary workers of
$998, divided by 40 hours to calculate
an hourly pre-tax wage rate of $24.95/
hour. This rate is adjusted downwards
by an estimate of the effective tax rate
for median income households of about
17 percent, resulting in the post-tax
hourly wage rate of $20.71/hour. Unlike
our State and private sector wage
adjustments, we are not adjusting
beneficiary wages for fringe benefits and
other indirect costs since the
individuals’ activities, if any, will occur
outside the scope of their employment.
255 We have previously estimated that labor
performed could be accomplished by Medical
Records and Health Information Technician staff
and note that this BLS occupation category has been
replaced with Medical Records Specialists.
256 https://aspe.hhs.gov/sites/default/files/
private/pdf/257746/VOT.pdf.
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A. Wage Estimates
To derive average costs for this FY
2024 IPF PPS final rule, we used data
from the U.S. Bureau of Labor Statistics’
(BLS’) May 2021 National Occupational
Employment and Wage Estimates for all
salary estimates (https://www.bls.gov/
oes/2021/may/oes292072.htm). In this
regard, Table 25 presents BLS’ median
hourly wage for Medical Records
Specialists 255 (the occupation title that
we have estimated is appropriate for
completing data collection and
reporting under the IPFQR Program),
our estimated cost of fringe benefits and
other indirect costs (calculated at 100
percent of salary), and our adjusted
hourly wage.
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Circumstances Exceptions policies. We
did not propose any changes to these
policies.
We proposed to codify the ECE
policies at § 412.433(f). As finalized,
paragraph (f) provides that we may grant
an exception to one or more data
submission deadlines and requirements
in the event of extraordinary
circumstances beyond the control of the
IPF either in response to a request by
the IPF or at our discretion if we
determine an extraordinary
circumstance occurred.
We solicited comments on our
proposal to codify these policies.
We did not receive any comments on
this proposal.
Final Decision: We are finalizing our
proposal to codify these policies.
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B. Information Collection Requirements
(ICRs) Regarding the IPFQR Program
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The following changes will be
submitted to OMB for approval under
control number 0938–1171 (CMS–
10432). We are not making changes to
any of the data collection instruments
that are currently approved under that
control number. We are, however,
adopting one new instrument, the
Psychiatric Inpatient Experience survey,
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to calculate the patient experience of
care measure described in section VI.D.5
of this final rule.
In section VII.B.1 of this final rule, we
restate our currently approved burden
estimates. In section VII.B.2 of this final
rule, we estimate the changes in burden
associated with the policies finalized in
this rule and updated estimates for wage
rates, facility counts, and case counts.
Then in section VII.B.3 of this final rule,
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we provide an overview of the total
estimated burden.
1. Currently Approved Burden
For a detailed discussion of the
burden for the IPFQR Program
requirements that we have previously
adopted, we refer readers to the FY 2022
IPF PPS final rule (86 FR 42661 through
42672).
Table 26 provides an overview of our
currently approved burden estimates.
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2. Adjustments Due to Changes in This
Final Rule
We are finalizing provisions that
impact policies beginning with the FY
2025 through FY 2028 payment
determinations. For the purposes of
calculating burden, we attribute the
costs to the year in which the costs
begin. For example, data submission for
the measures that affect the FY 2025
payment determination occurs during
CY 2024 and generally reflects care
provided during CY 2023. The following
discussion describes the burden changes
for policies attributed to the year in
which the costs begin. For the policies
in this final rule, those years are CY
2024 through CY 2027.
Additionally, in the FY 2022 IPF PPS
final rule (86 FR 42661 through 42672),
which is the most recent rule that
updated the IPFQR Program policies, we
estimated that there were 1,634
participating IPFs and that (for measures
that require reporting on the entire
patient population) these IPFs will
report on an average of 1,346 cases per
IPF. In this FY 2024 IPF PPS final rule,
we are adjusting our IPF count and case
estimates by using the most recent data
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available. Specifically, we estimate that
there are now approximately 1,596
facilities (a decrease of 38 facilities) and
an average of 1,261 cases per facility (a
decrease of 85 cases per facility). We
will update our estimates, as applicable,
using these revised estimates in the
following subsections.
that control number, including those of
the COVID–19 Vaccination Coverage
Among HCP measure.
a. Policies Affecting Data Reporting
Beginning in CY 2023
In section VI.E. of this final rule, we
are modifying the COVID–19
Vaccination Coverage Among
Healthcare Personnel (HCP) measure
beginning with data reflecting the fourth
quarter of CY 2023 affecting the FY 2025
payment determination. We do not
believe that this modification (that is, a
change in terminology to refer to ‘‘upto-date’’ instead of ‘‘complete
vaccination course’’) will impact our
currently approved IPF information
collection requirements or burden
estimates because the modified measure
will be calculated using data already
being submitted by IPFs to the CDC for
healthcare safety surveillance under the
CDC’s OMB control number 0920–1317.
In this regard, the CDC owns the
requirements and burden that fall under
In section VI.F.2 of this final rule, we
are removing two measures beginning
with the FY 2025 payment
determination. Data for these measures
would have been submitted in CY 2024,
so we are estimating the reduced burden
to occur in CY 2024. The two measures
are:
• Patients Discharged on Multiple
Antipsychotic Medications with
Appropriate Justification (HBIPS–5);
and
• Tobacco Use Treatment Provided or
Offered and Tobacco Use Treatment
(TOB–2 and TOB–2a).
Using our currently approved burden
estimates as a baseline, the changes
associated with removing these
measures are: a decrease of 1,990,212
responses, a decrease of 497,553 hours,
and a decrease of $20,339,673 as set
forth in Table 27.
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b. Policies Affecting Burden Beginning
With CY 2024
(1) Updates Affecting Facility Reporting
Burden
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Additionally, we are applying our
updated wage rate (from $41.00/hour to
$44.86/hour), case count (from 1,346 to
1,261), and facility counts (from 1,634 to
1,596) to the remaining measure set and
program requirements for data
submission in CY 2024. See Table 28
and 29 for information on the effects of
these updates. Specifically, we estimate
that there are now approximately 1,596
facilities (a decrease of 38 facilities) and
an average of 1,261 cases per facility (a
decrease of 85 cases per facility). We
also estimate a wage increase of $3.86/
hour as described in section VI.A of this
final rule. Our previous estimate shows
that the two measures which do not
allow sampling had 1,346 cases per
measure and the six remaining measures
which do allow sampling require 609
cases per measure per facility. We have
estimated that these measures will take
0.25 hours per case. The effects of the
updated hourly wage are set forth in
Table 28.
The remaining calculations will use
the updated hourly wage to calculate
the effects of other updates.
Our active burden estimates account
for 1,346 cases for measures that do not
allow sampling. Based on more recent
data, we are updating our estimate for
measures that do not allow sampling to
1,261 cases per IPF (a decrease of 85
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cases for each of the 2 measures which
do not allow sampling). This is
equivalent to 138,890 cases across the
1,634 IPFs (85 cases × 1,634 IPFs) in our
previous estimate for each measure. We
are not changing our estimated case
counts for measures that allow
sampling. We continue to assume an
average of 0.25 hours of effort per case.
Therefore, this change in cases reflects
a total annual effort of 42.5 hours per
facility (2 measures * 85 cases per
measure * 0.25 hours per case) at a cost
of $1,907 (42.5 hours * $44.86/hour).
As indicated above we estimate a
reduction of 38 facilities based on
updated numbers. Table 29 shows the
effects of this reduction in facilities on
the reporting burden associated with
each measure type.
We note that at 6,180 cases per
facility, removing 38 facilities from our
estimate removes a total of 234,840
cases (6,180 cases per facility * 38
facilities).
The total effects of changes for the CY
2024 calendar year on our burden
estimates are summarized in Table 30.
(2) Updates Affecting Patient Survey
Burden
In section VI.D.3 of this final rule, we
are adopting the Screening for Social
Drivers of Health measure beginning
with a voluntary data submission in CY
2025 (reflecting care provided in CY
2024). IPFs will be able to collect data
and report the measure via multiple
methods, potentially including
administrative claims data, electronic
clinical data, standardized patient
assessments, or patient-reported data
and surveys. For additional information
on these methods, we refer readers to
section VI.D.3.c of this final rule. We
believe that most IPFs will likely collect
data during the patient intake process.
Because this measure reflects care
provided in CY 2024, the burden for
administering the screening to patients
will occur during CY 2024.
Under OMB Control Number 0938–
1022 (CMS–10210) and the FY 2022
IPPS/LTCH PPS final rule (87 FR 49385
through 49386), the Hospital IQR
Program, which adopted the Screening
for Social Drivers of Health measure,
estimates that it will take 2 minutes
(0.033 hr) per patient to complete the
selected screening instrument. The
Hospital IQR Program also estimated
that during the voluntary reporting
period roughly 50 percent of hospitals
will survey 50 percent of patients (87 FR
49385 through 49386).
We agree with these estimates and
believe that a similar proportion of IPFs
will participate in the voluntary
reporting period. As described in
section VII.A of this final rule, we
estimate the cost of patients’ time for
completing surveys to be $20.71/hour.
Using these estimates, we believe that
during the voluntary reporting period
the annual burden of surveying IPF
patients will be 503,139 responses
[(1,596 facilities × 50 percent of
facilities) × (1,261 patients per facility ×
50 percent of patients)], 16,604 hours
(503,139 responses × 0.033 hours/
response] at a cost of $343,869 (16,604
hours × $20.71/hour). These estimates
are summarized in Table 31.
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c. Policies Affecting Burden Beginning
With CY 2025
(1) Updates Affecting Facility Reporting
Burden
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because this burden will accrue during
CY 2024. The burden associated with
reporting each of these measures to CMS
will occur during CY 2025. We
anticipate that the burden for reporting
the two measures will be consistent
with the burden for other web-based
submissions, such as the Facility
Commitment to Health Equity measure
described previously in this section and
for similar measures adopted in the
Ambulatory Surgical Center Quality
Reporting (ASCQR) Program (OMB
control number 0938–1270; CMS–
10530), which we have estimated to
have a reporting burden of 10 minutes
(0.167 hours) per facility. We note that
for the voluntary reporting year we have
estimated only 50 percent or 798 IPFs
(1,596 IPFs × 0.50) will report these
data. Therefore, we estimate the burden
associated with reporting of each of
these measures to be 133 hours (0.167
hr. × 798 IPFs) at a cost of $5,966 (133
hr. × $44.86/hour) for a medical records
specialist) for the voluntary reporting
period. These estimates are summarized
in Table 32.
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In section VI.I.5 of this final rule, we
are adopting a data validation pilot for
the IPFQR Program. Under this pilot we
will reimburse hospitals directly for
expenses associated with submission of
charts for clinical process of care
measure data validation. Because we
will reimburse facilities directly for
these expenses we do not believe that
this pilot will increase information
collection burden.
In section VI.D.2. of this final rule, we
are adopting the Facility Commitment to
Health Equity measure beginning with
the FY 2026 payment determination.
Data for this attestation measure will be
submitted during CY 2025. Consistent
with our burden estimate from the
Hospital IQR Program, when we
adopted the similar Hospital
Commitment to Health Equity measure
in the FY 2023 IPPS/LTCH PPS final
rule, we estimated an average of 10
minutes per facility for a medical
records specialist to collect and report
this information (87 FR 49385). We
recognize that some IPFs may take more
than 10 minutes to collect this
information, especially in the first year
of reporting; however, we believe that
many IPFs will require less than 10
minutes. In addition, we believe that
many IPFs will be able to submit similar
responses in future years. Using the
estimate of 10 minutes (0.167 hour) per
IPF per year at $44.86/hour for a
medical records specialist, we estimate
that this policy will result in a total
annual burden increase of 267 hours
(0.167 hours × 1,596 IPFs) at a cost of
$11,956.63 (267 hours × $44.86/hour)
across all participating IPFs.
In sections VI.D.3 and VI.D.4 of this
final rule, we are adopting the Screening
for Social Drivers of Health measure and
the associated Screen Positive Rate for
Social Drivers of Health measure
beginning with a voluntary data
submission in CY 2025 (reflecting care
provided in CY 2024). We described our
anticipated burden (16,604 hours at a
cost of $343,869) for administering the
screening in the previous section
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(2) Updates Affecting Patient Survey
Burden
Beginning with CY 2025, IPFs will
need to screen 100 percent of their
patients to prepare for mandatory
reporting of the Screening for Social
Drivers of Health measure in CY 2026
(for the FY 2027 payment
determination). Therefore, we estimate
that 100 percent of IPFs will screen 100
percent of their patients. We recognize
that this may be an overestimate as
some IPFs may choose not to participate
and some patients may opt out of
screening or be unable to provide
responses; however, we believe that the
numbers of IPFs and patients opting out
will be relatively small and therefore
100 percent will be a reasonable
approximation.
Using the facility counts (1,596
facilities), patient counts (1,261 patients
per facility), average hourly earnings
($20.71/hour), and time per response
(10 min or 0.033 hours) described
previously, we estimate the burden of
surveying IPF patients for health-related
social needs (HRSNs) under the
Screening for Social Drivers of Health
and Screen Positive Rate for Social
Drivers of Health measures will be
66,414 hours (1,596 facilities × 1,261
patients per facility × 0.033 hr) at a cost
of $1,375,434 (66,414 hour × $20.71/
hour) across all patients. We note that
16,604 hours and $343,960 of this
burden was accounted for in our
analysis of the burden of the voluntary
reporting period described in section
VII.B.2.c.(2). Therefore, the incremental
burden of switching to mandatory
reporting is 49,810 hours (66,414 hours–
16,604 hours) and $1,031,474
($1,375,434–$343,960).
Additionally, in section VI.D.5 of this
final rule, we are adopting the
Psychiatric Inpatient Experience (PIX)
survey measure beginning with
voluntary data submission in CY 2026.
To prepare for data submission in 2026,
IPFs will begin administering this
survey in CY 2025. We believe 50
percent or 798 (1,596 facilities × 0.50) of
IPFs would begin collecting these data
for the voluntary data submission
period. We note that we proposed to
allow IPFs with more than 300 eligible
discharges to sample, which would
require these facilities to survey 300
patients. Because the questions on the
PIX survey are similar in content and
response options to the questions on the
Hospital Consumer Assessment of
Healthcare Providers and Systems
(HCAHPS) survey, we believe that it
will take patients a similar amount of
time to respond to these questions. In
the Information Collection Request
associated with OMB control number
0938–0981 (CMS–10102), we have
estimated this time to be 7.25 minutes
(0.121 hours).
Therefore, we believe that the burden
associated with conducting the PIX
survey in CY 2025 will be 28,967 hours
(798 facilities × 300 patients/facility ×
0.121 hours/response) at a cost of
$599,907 (28,967 hours × $20.71/hour).
Our estimates for the CY 2025 total
patient survey burden changes are
summarized in Table 33.
d. Policies Affecting Burden Beginning
With CY 2026
accounted for 50 percent of facilities
submitting voluntary data on these
measures, the incremental burden is the
burden associated with the remaining
50 percent of facilities submitting data;
that is, we estimate this burden to be
266 hours at a cost of $11,933. We also
believe that 50 percent of facilities will
submit data on the PIX survey measure
for the voluntary reporting period in CY
2025. Because the data for this measure
will require calculating an average of
scores across a sample of patient
surveys, we anticipate that the
information collection and reporting
burden for this measure will be
approximately 15 minutes (0.25 hours)
per patient for whom they are reporting
data. The burden associated with
reporting the Screening for Social
Drivers of Health measure, the Screen
Positive Rate for Social Drivers of
Health measure, and the PIX survey
measure to CMS is described in Table
34.
(1) Updates Affecting Facility Reporting
Burden
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Beginning with CY 2026 data
submission (affecting the FY 2027
payment determination), we estimate
that 100 percent of IPFs will submit data
on the Screening for Social Drivers of
Health measure and Screen Positive
Rate for Social Drivers of Health
measure. Because we have already
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(2) Updates Affecting Patient Survey
Burden
Because reporting the PIX survey
measure will be mandatory for the FY
2028 payment determination, the
remaining 50 percent of facilities (those
which did not participate in the
voluntary reporting period) will begin
surveying patients in CY 2026. To
prepare for data submission of the PIX
survey measure to CMS in CY 2027,
IPFs that had not previously begun
administering the PIX survey will begin
administering this survey in CY 2026.
The incremental burden of these 50
percent of facilities administering the
survey will be equivalent to the burden
associated with the 50 percent of
facilities that participated in the
voluntary reporting in CY 2025. These
estimates are summarized in Table 35.
e. Policies Affecting Facility Reporting
Burden Beginning With CY 2027
we believe that an additional 50 percent
of facilities will report the measure (that
is, the 50 percent of facilities not
previously accounted for under the
voluntary reporting period). Therefore,
we estimate that the incremental
increase in burden for IPFs associated
with this requirement will be reporting
by the 50 percent of facilities that had
not previously reported the PIX survey
measure. This burden is set forth in
Table 36.
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For data submission occurring in CY
2027, submission on the PIX survey
measure will be mandatory, therefore,
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3. Overall Burden Summary
with policies for data collection and
submission in CYs 2024 through 2027 as
well as updates to our estimated wage
rate, facility counts, and case counts.
Table 38 summarizes the incremental
changes in burden for patients due to
data collection associated with
proposed policies for data collection
and submission in CYs 2024 through CY
2026.
Table 39 summarizes the total annual
change in burden associated with the
IPFQR Program’s finalized policies in
this final rule. These figures are
calculated by adding the annual changes
in Table 37 with the annual changes in
Table 38. We note that these figures
represent the changes to our previously
approved burden (set forth in Table 26
of this final rule).
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Table 37 summarizes the incremental
changes in burden for IPFs associated
C. Comments Received on the Proposed
Collection of Information Requirements
We solicited public comment on our
estimated burden associated with the
information collection requirements.
The following comments were
received.
Comment: Several commenters
expressed concern that the policies
under the IPFQR Program will be
burdensome, and some commenters
specifically noted burden related to the
PIX survey. One commenter expressed
the belief that removing two measures
while adopting four measures would
increase overall burden.
Response: We understand
commenters’ concerns that some of the
policies under the IPFQR Program may
contribute to IPF reporting burden. With
respect to the PIX survey, we do not
believe that administering a patient
experience of care survey will be
unduly burdensome for the majority of
IPFs that previously self-reported that
they already administer such a survey
when responding to the IPFQR
Program’s former Assessment of Patient
Experience of Care measure. We
recognize that there will be some nonrecurring burden for these IPFs to
transition to the newly adopted survey.
With respect to the concern that
removing two measures while adopting
four measures would increase the
overall burden, we note that the
measures we are removing are chartabstracted measures with high reporting
burden. We estimate that the newly
adopted measures require less time to
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calculate and report. Therefore, we
believe that our estimate that the overall
burden of the IPFQR Program will be
decreased by these policies is accurate.
VIII. Regulatory Impact Analysis
A. Statement of Need
This rule finalizes updates to the
prospective payment rates for Medicare
inpatient hospital services provided by
IPFs for discharges occurring during FY
2024 (October 1, 2023 through
September 30, 2024). We are finalizing
our proposal to apply a 2021-based IPF
market basket increase for FY 2024 of
3.5 percent, less the productivity
adjustment of 0.2 percentage point as
required by 1886(s)(2)(A)(i) of the Act
for a final total FY 2024 payment rate
update of 3.3 percent. In this final rule,
we are finalizing our proposal to update
the outlier fixed dollar loss threshold
amount, update the IPF labor-related
share, and update the IPF wage index to
reflect the FY 2024 hospital inpatient
wage index. Section 1886(s)(3)(4) of the
Act requires IPFs to report data in
accordance with the requirements of the
IPFQR Program for purposes of
measuring and making publicly
available information on health care
quality, and links the quality data
submission to the annual applicable
percentage increase.
B. Overall Impact
We have examined the impacts of this
rule as required by Executive Order
12866 on Regulatory Planning and
Review (September 30, 1993), Executive
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Order 13563 on Improving Regulation
and Regulatory Review (January 18,
2011), Executive Order 14094 entitled
‘‘Modernizing Regulatory Review’’
(April 6, 2023), the Regulatory
Flexibility Act (RFA) (September 19,
1980, Pub. L. 96–354), section 1102(b) of
the Social Security Act, section 202 of
the Unfunded Mandates Reform Act of
1995 (March 22, 1995; Pub. L. 104–4),
Executive Order 13132 on Federalism
(August 4, 1999), and the Congressional
Review Act (5 U.S.C. 804(2)).
Executive Orders 12866 and 13563
direct agencies to assess all costs and
benefits of available regulatory
alternatives and, if regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety
effects, distributive impacts, and
equity). The Executive Order 14094
entitled ‘‘Modernizing Regulatory
Review’’ (hereinafter, the Modernizing
E.O.) amends section 3(f)(1) of Executive
Order 12866 (Regulatory Planning and
Review). The amended section 3(f) of
Executive Order 12866 defines a
‘‘significant regulatory action’’ as an
action that is likely to result in a rule:
(1) having an annual effect on the
economy of $200 million or more in any
1 year (adjusted every 3 years by the
Administrator of OIRA for changes in
gross domestic product), or adversely
affect in a material way the economy, a
sector of the economy, productivity,
competition, jobs, the environment,
public health or safety, or State, local,
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territorial, or tribal governments or
communities; (2) creating a serious
inconsistency or otherwise interfering
with an action taken or planned by
another agency; (3) materially altering
the budgetary impacts of entitlement
grants, user fees, or loan programs or the
rights and obligations of recipients
thereof; or (4) raising legal or policy
issues for which centralized review
would meaningfully further the
President’s priorities or the principles
set forth in the order, as specifically
authorized in a timely manner by the
Administrator of OIRA in each case.
A regulatory impact analysis (RIA)
must be prepared for major rules with
significant regulatory action(s) and/or
with significant effects as per section
3(f)(1) ($200 million or more in any 1
year). We estimate that the total impact
of these changes for FY 2024 payments
compared to FY 2023 payments will be
a net increase of approximately $70
million. This reflects a $95 million
increase from the update to the payment
rates (+$100 million due to the FY
2024IPF market basket update of 3.5
percent, and ¥$5 million for the
productivity adjustment of 0.2
percentage point), as well as a $25
million decrease as a result of the
update to the outlier threshold amount.
Outlier payments are estimated to
change from 2.9 percent in FY 2023 to
2.0 percent of total estimated IPF
payments in FY 2024.
Based on our estimates, OMB’s Office
of Information and Regulatory Affairs
has determined that this rulemaking is
not significant per section 3(f)(1) as
measured by the $200 million threshold
or more in any 1 year. Nevertheless, this
rule is a major rule, and accordingly, we
have prepared a Regulatory Impact
Analysis that to the best of our ability
presents the costs and benefits of the
rulemaking. Therefore, OMB has
reviewed this final regulation, and we
have provided the following assessment
of its impact.
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C. Detailed Economic Analysis
In this section, we discuss the
historical background of the IPF PPS
and the impact of this final rule on the
Federal Medicare budget and on IPFs.
1. Budgetary Impact
As discussed in the November 2004
and RY 2007 IPF PPS final rules, we
applied a budget neutrality factor to the
Federal per diem base rate and ECT
payment per treatment to ensure that
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total estimated payments under the IPF
PPS in the implementation period will
equal the amount that would have been
paid if the IPF PPS had not been
implemented. This Budget neutrality
factor included the following
components: Outlier adjustment, stop
loss adjustment, and the behavioral
offset. As discussed in the RY 2009 IPF
PPS notice (73 FR 25711), the stop-loss
adjustment is no longer applicable
under the IPF PPS.
As discussed in section III.D.1 of this
final rule, we proposed to update the
wage index and labor-related share in a
budget neutral manner by applying a
wage index budget neutrality factor to
the Federal per diem base rate and ECT
payment per treatment. Therefore, the
budgetary impact to the Medicare
program of this final rule will be due to
the IPF market basket update for FY
2024 of 3.5 percent (see section IV.A.2
of this final rule) reduced by the
productivity adjustment of 0.2
percentage point as required by section
1886(s)(2)(A)(i) of the Act and the
update to the outlier fixed dollar loss
threshold amount.
We estimate that the FY 2024 impact
will be a net increase of $70 million in
payments to IPF providers. This reflects
an estimated $95 million increase from
the update to the payment rates and a
$25 million decrease due to the update
to the outlier threshold amount to set
total estimated outlier payments at 2.0
percent of total estimated payments in
FY 2024. This estimate does not include
the implementation of the mandatory
2.0 percentage point reduction of the
productivity-adjusted IPF market basket
update factor for any IPF that fails to
meet the IPF quality reporting
requirements (as discussed in section
IV.B.2. of this final rule).
2. Impact on Providers
To show the impact on providers of
the changes to the IPF PPS discussed in
this final rule, we compare estimated
payments under the proposed IPF PPS
rates and factors for FY 2024 versus
those under FY 2023. We determined
the percent change in the estimated FY
2024 IPF PPS payments compared to the
estimated FY 2023 IPF PPS payments
for each category of IPFs. In addition,
for each category of IPFs, we have
included the estimated percent change
in payments resulting from the final
update to the outlier fixed dollar loss
threshold amount; the updated wage
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index data including the final laborrelated share; and the final IPF market
basket update for FY 2024, as reduced
by the final productivity adjustment
according to section 1886(s)(2)(A)(i) of
the Act.
To illustrate the impacts of the FY
2024 changes in this final rule, our
analysis begins with FY 2022 IPF PPS
claims (based on the 2022 MedPAR
claims, March 2023 update). We
estimate FY 2023 IPF PPS payments
using these 2022 claims, the finalized
FY 2023 IPF PPS Federal per diem base
rates, and the finalized FY 2023 IPF PPS
patient and facility level adjustment
factors (as published in the FY 2023 IPF
PPS final rule (87 FR 46846)). We then
estimate the FY 2024 outlier payments
based on these simulated FY 2023 IPF
PPS payments using the same
methodology that we used to set the
initial outlier threshold amount in the
RY 2007 IPF PPS final rule (71 FR 27072
and 27073), which is also the same
methodology that we used to update the
outlier threshold amounts for years 2008
through 2022, where total outlier
payments are maintained at 2 percent of
total estimated FY 2023 IPF PPS
payments. We note that in the FY 2023
final rule (87 FR 46862 through 46864)
we excluded providers from our
simulation of IPF PPS payments for FY
2022 and FY 2023 if their change in
estimated average cost per day was
outside 3 standard deviations from the
mean. As discussed in section IV.E.2 of
this final rule, we did not propose to
apply this methodology for FY 2024.
Each of the following changes is
added incrementally to this baseline
model in order for us to isolate the
effects of each change:
• The update to the outlier fixed
dollar loss threshold amount.
• The FY 2024 IPF wage index and
the FY 2024 labor-related share.
• The IPF market basket update for
FY 2024 of 3.5 percent less the
productivity adjustment of 0.2
percentage point in accordance with
section 1886(s)(2)(A)(i) of the Act for a
final IPF payment rate update of 3.3
percent.
Our column comparison in Table 40
illustrates the percent change in
payments from FY 2023 (that is, October
1, 2022, to September 30, 2023) to FY
2024 (that is, October 1, 2023, to
September 30, 2024) including all the
payment policy changes.
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3. Impact Results
Table 40 displays the results of our
analysis. The table groups IPFs into the
categories listed here based on
characteristics provided in the Provider
of Services file, the IPF PSF, and cost
report data from the Healthcare Cost
Report Information System:
• Facility Type.
• Location.
• Teaching Status Adjustment.
• Census Region.
• Size.
The top row of the table shows the
overall impact on the 1,479 IPFs
included in the analysis. In column 2,
we present the number of facilities of
each type that had information available
in the PSF and had claims in the
MedPAR dataset for FY 2022.
In column 3, we present the effects of
the update to the outlier fixed dollar
loss threshold amount. We estimate that
IPF outlier payments as a percentage of
total IPF payments are 2.9 percent in FY
2023. Therefore, we adjusted the outlier
threshold amount to set total estimated
outlier payments equal to 2.0 percent of
total payments in FY 2024. The
estimated change in total IPF payments
for FY 2024, therefore, includes an
approximate 0.9 percent decrease in
payments because we expect the outlier
portion of total payments to decrease
from approximately 2.9 percent to 2.0
percent.
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The overall impact of the estimated
decrease to payments due to updating
the outlier fixed dollar loss threshold (as
shown in column 3 of Table 3), across
all hospital groups, is a 0.9 percentage
point decrease. The largest decrease in
payments due to this change is
estimated to be 2.6 percent for urban
government unit IPFs.
In column 4, we present the effects of
the budget-neutral update to the IPF
wage index, the Labor-Related Share
(LRS), and the 5-percent cap on any
decrease to a provider’s wage index
from its wage index in the prior year.
This represents the effect of using the
concurrent hospital wage data as
discussed in section IV.D.1.a of this
final rule. That is, the impact
represented in this column reflects the
update from the FY 2023 IPF wage
index to the FY 2024 IPF wage index,
which includes basing the FY 2024 IPF
wage index on the FY 2024 pre-floor,
pre-reclassified IPPS hospital wage
index data, applying a 5-percent cap on
any decrease to a provider’s wage index
from its wage index in the prior year,
and updating the LRS from 77.4 percent
in FY 2023 to 78.7 percent in FY 2024.
We note that there is no projected
change in aggregate payments to IPFs, as
indicated in the first row of column 4;
however, there will be distributional
effects among different categories of
IPFs. For example, we estimate the
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largest increase in payments to be 1.1
percent for Mid-Atlantic IPFs, and the
largest decrease in payments to be 1.3
percent for freestanding, rural, for-profit
IPFs.
Column 5 incorporates the FY 2024
IPF market basket update of 3.5 percent
reduced by 0.2 percentage point for the
productivity adjustment as required by
section 1886(s)(2)(A)(i) of the Act. This
includes rebasing the IPF market basket
to reflect a 2021 base year.
Overall, IPFs are estimated to
experience a net increase in payments
as a result of the updates in this final
rule. IPF payments are estimated to
increase by 2.4 percent in urban areas
and 2.0 percent in rural areas. The
largest payment increases are estimated
at 3.4 percent for freestanding, urban,
non-profit IPFs.
4. Effect on Beneficiaries
Under the FY 2024 IPF PPS, IPFs will
continue to receive payment based on
the average resources consumed by
patients for each day. Our longstanding
payment methodology reflects the
differences in patient resource use and
costs among IPFs, as required under
section 124 of the BBRA. We expect that
updating IPF PPS rates in this final rule
will improve or maintain beneficiary
access to high quality care by ensuring
that payment rates reflect the best
available data on the resources involved
in inpatient psychiatric care and the
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costs of these resources. We continue to
expect that paying prospectively for IPF
services under the FY 2024 IPF PPS will
enhance the efficiency of the Medicare
program.
As discussed in sections VI.D.3 and
VI.D.4 of this final rule, we expect that
additional IPFQR Program measures
will support improving care for patients
with health-related social needs. We
also believe that our data validation
pilot is an important step towards
ensuring that the data beneficiaries and
their caregivers access on Care Compare
(or a successor CMS website) are
accurate and reliable. Based on the
input from patients and their caregivers
regarding the importance of having a
patient experience of care measure for
the IPF setting in which they note many
benefits (including, but not limited to
helping patients select facilities in
which to receive care, providing
patients an opportunity to be heard, and
increasing alignment between general
acute and acute psychiatric settings).
We believe that our PIX survey measure
will have positive effects on patients
and their caregivers. Therefore, we
expect that the updates to the IPFQR
Program will improve quality for
beneficiaries.
5. Effects of the Updates to the IPFQR
Program
In section VI.D.3 of this final rule, we
are adopting the Screening for Social
Drivers of Health measure for the IPFQR
Program beginning with voluntary
reporting of CY 2024 data, and with
mandatory reporting of CY 2025 data for
the FY 2027 payment determination.
For IPFs that are not currently
administering some screening
mechanism and elect to begin doing so
as a result of this policy, there will be
some non-recurring costs associated
with changes in workflow and
information systems to collect the data.
The extent of these costs is difficult to
quantify as different facilities may
utilize different modes of data collection
(for example, paper-based,
electronically patient-directed and
clinician-facilitated). In addition,
depending on the method of data
collection utilized, the time mandatory
to complete the survey may add a
negligible amount of time to patient
visits.
In section VI.D.5 of this final rule, we
are adopting the Psychiatric Inpatient
Experience (PIX) survey measure. There
may be some non-recurring costs
associated with changes in workflow
and information systems to administer
this survey and collect the data. The
extent of these costs is difficult to
quantify as different facilities currently
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have different practices for surveying
patients to gather information on their
experiences of care.
In addition, for the IPFQR Program,
we are adopting the Facility
Commitment to Health Equity measure
and the Screen Positive for Social
Drivers of Health measure, as well as to
update the COVID–19 Vaccination
Coverage Among HCP measure. These
updates will not impact providers
workflows or information systems to
collect or report the data, and because
they represent processes of care or
structural data that the IPFs will already
have in place, we do not believe they
will incur costs for providers beyond
the recurring information collection
costs (described in section VII.B of this
final rule).
Finally, we are removing two chartabstracted measures from the IPFQR
Program. We believe that the impact of
removing the Tobacco Use Brief
Intervention Provided or Offered and
Tobacco Use Brief Intervention
Provided (TOB–2/2a) measure will be
minimal as we do not believe that IPFs
will update their workflow to no longer
provide brief tobacco cessation
interventions to patients who use
tobacco. However, we believe that there
may be some simplification of
workflows and clinical documentation
associated with the removal of the
Patients Discharged on Multiple
Antipsychotic Medications with
Appropriate Justification (HBIPS–5)
measure because IPFs will no longer
have to ensure the presence of
appropriate documentation for the use
of multiple antipsychotics. For more
information on the updated clinical
guidelines regarding polypharmacy for
patients with schizophrenia, we refer
readers to section VI.F.2.a of this final
rule.
As discussed in section IV.B.2 of this
final rule and in accordance with
section 1886(s)(4)(A)(i) of the Act, we
will apply a 2-percentage point
reduction to the FY 2024 market basket
update for IPFs that have failed to
comply with the IPFQR Program
requirements for FY 2024, including
reporting on the mandatory measures. In
section IV.B.2 of this final rule, we
discuss how the 2-percentage point
reduction will be applied. For the FY
2023 payment determination, of the
1,596 IPFs eligible for the IPFQR
Program, 6 IPFs did not receive the full
market basket update because of the
IPFQR Program; 2 of these IPFs chose
not to participate and 4 did not meet the
requirements of the program. Thus, we
estimate that the IPFQR Program will
have a negligible impact on overall IPF
payments for FY 2024.
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Based on the IPFQR Program policies
in this final rule, we estimate a total
decrease in burden of 380,897 hours
across all IPFs, resulting in a total
decrease in information collection cost
of $8.15 million across all IPFs. Further
information on these estimates can be
found in section VII.B of this final rule.
We intend to closely monitor the
effects of the IPFQR Program on IPFs
and help facilitate successful reporting
outcomes through ongoing stakeholder
education, national trainings, and a
technical help desk.
6. Regulatory Review Costs
If regulations impose administrative
costs on private entities, such as the
time needed to read and interpret this
final rule, we should estimate the cost
associated with regulatory review. Due
to the uncertainty involved with
accurately quantifying the number of
entities that will be directly impacted
and will review this final rule, we
assume that the total number of unique
commenters on the most recent IPF PPS
proposed rule will be the number of
reviewers of this final rule. For this FY
2024 IPF PPS final rule, the most recent
IPF PPS proposed rule was the FY 2024
IPF PPS proposed rule, and we received
2,506 unique comments on this
proposed rule. We acknowledge that
this assumption may understate or
overstate the costs of reviewing this
final rule. It is possible that not all
commenters reviewed the FY 2024 IPF
PPS proposed rule in detail, and it is
also possible that some reviewers chose
not to comment on that proposed rule.
For these reasons, we thought that the
number of commenters will be a fair
estimate of the number of reviewers
who are directly impacted by this final
rule. We solicited comments on this
assumption.
We also recognize that different types
of entities are in many cases affected by
mutually exclusive sections of this final
rule; therefore, for the purposes of our
estimate, we assume that each reviewer
reads approximately 50 percent of this
final rule. Using the May, 2022 mean
(average) wage information from the
BLS for medical and health service
managers (Code 11–9111), we estimate
that the cost of reviewing this final rule
is $123.06 per hour, including overhead
and fringe benefits https://www.bls.gov/
oes/current/oes119111.htm. Assuming
an average reading speed of 250 words
per minute, we estimate that it will take
approximately 198 minutes (3.3 hours)
for the staff to review half of this final
rule (49,500), which contains a total of
approximately 99,000 words. For each
IPF that reviews the final rule, the
estimated cost is (3.3 × $123.06) or
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$406.10. Therefore, we estimate that the
total cost of reviewing this final rule is
$1,017,686.60 ($406.10 × 2,506
reviewers).
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D. Alternatives Considered
The statute does not specify an update
strategy for the IPF PPS and is broadly
written to give the Secretary discretion
in establishing an update methodology.
We continue to believe it is appropriate
to routinely update the IPF PPS so that
it reflects the best available data about
differences in patient resource use and
costs among IPFs as required by the
statute. Therefore, we are finalizing our
proposal to: Update the IPF PPS using
the methodology published in the
November 2004 IPF PPS final rule;
F. Regulatory Flexibility Act
The RFA requires agencies to analyze
options for regulatory relief of small
entities if a rule has a significant impact
on a substantial number of small
entities. For purposes of the RFA, small
entities include small businesses,
nonprofit organizations, and small
governmental jurisdictions. Most IPFs
and most other providers and suppliers
are small entities, either by nonprofit
status or having revenues of $8 million
to $41.5 million or less in any 1 year.
Individuals and states are not included
in the definition of a small entity.
Because we lack data on individual
hospital receipts, we cannot determine
the number of small proprietary IPFs or
the proportion of IPFs’ revenue derived
from Medicare payments. Therefore, we
assume that all IPFs are considered
small entities.
The Department of Health and Human
Services generally uses a revenue
impact of 3 to 5 percent as a significance
threshold under the RFA. As shown in
Table 40, we estimate that the overall
revenue impact of this final rule on all
IPFs is to increase estimated Medicare
payments by 2.3 percent. As a result,
since the estimated impact of this final
rule is a net increase in revenue across
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apply the 2021-based IPF market basket
update for FY 2024 of 3.5 percent
reduced by the productivity adjustment
of 0.2 percentage point as required by
section 1886(s)(2)(A)(i) of the Act along
with the wage index budget neutrality
adjustment to update the payment rates;
and use a FY 2024 IPF wage index
which uses the FY 2024 pre-floor, prereclassified IPPS hospital wage index as
its basis.
Lastly, we solicited comments on
alternative methodologies that could be
appropriate for establishing the FY 2024
outlier fixed dollar loss threshold.
E. Accounting Statement
As required by OMB Circular A–4
(https://www.whitehouse.gov/wp-
almost all categories of IPFs, the
Secretary has determined that this final
rule will have a positive revenue impact
on a substantial number of small
entities.
In addition, section 1102(b) of the Act
requires us to prepare a regulatory
impact analysis if a rule may have a
significant impact on the operations of
a substantial number of small rural
hospitals. This analysis must conform to
the provisions of section 604 of the
RFA. For purposes of section 1102(b) of
the Act, we define a small rural hospital
as a hospital that is located outside of
a metropolitan statistical area and has
fewer than 100 beds. As discussed in
section VIII.C.2 of this final rule, the
rates and policies set forth in this final
rule will not have an adverse impact on
the rural hospitals based on the data of
the 211 rural excluded psychiatric units
and 61 rural psychiatric hospitals in our
database of 1,479 IPFs for which data
were available. Therefore, the Secretary
has determined that this final rule will
not have a significant impact on the
operations of a substantial number of
small rural hospitals.
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content/uploads/legacy_drupal_files/
omb/circulars/A4/a-4.pdf), in Table 41,
we have prepared an accounting
statement showing the classification of
the expenditures associated with the
updates to the IPF wage index and
payment rates in this final rule. Table 41
provides our best estimate of the
increase in Medicare payments under
the IPF PPS as a result of the changes
presented in this final rule and is based
on 1,479 IPFs with data available in the
PSF and with claims in our FY 2022
MedPAR claims dataset. Lastly, Table
41 also includes our best estimate of the
costs of reviewing and understanding
this final rule.
G. Unfunded Mandate Reform Act
(UMRA)
Section 202 of the Unfunded
Mandates Reform Act of 1995 (UMRA)
also requires that agencies assess
anticipated costs and benefits before
issuing any rule whose mandates
require spending in any 1 year of $100
million in 1995 dollars, updated
annually for inflation. In 2023, that
threshold is approximately $177
million. This final rule does not
mandate any requirements for state,
local, or tribal governments, or for the
private sector. This final rule will not
impose a mandate that will result in the
expenditure by state, local, and tribal
governments, in the aggregate, or by the
private sector, of more than $177
million in any 1 year.
H. Federalism
Executive Order 13132 establishes
certain requirements that an agency
must meet when it promulgates a
proposed rule that imposes substantial
direct requirement costs on state and
local governments, preempts state law,
or otherwise has Federalism
implications. This final rule does not
impose substantial direct costs on state
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or local governments or preempt state
law.
Chiquita Brooks-LaSure,
Administrator of the Centers for
Medicare & Medicaid Services,
approved this document on July 24,
2023.
List of Subjects in 42 CFR Part 412
Administrative practice and
procedure, Health facilities, Medicare,
Puerto Rico, Reporting and
recordkeeping requirements.
For the reasons set forth in the
preamble, the Centers for Medicare &
Medicaid Services amends 42 CFR part
412 as set forth below:
PART 412—PROSPECTIVE PAYMENT
SYSTEMS PROSPECTIVE PAYMENT
SYSTEMS FOR INPATIENT HOSPITAL
SERVICES
1. The authority citation for part 412
continues to read as follows:
■
Authority: 42 U.S.C. 1302 and 1395hh.
2. Section 412.25 is amended by
revising paragraph (c) to read as follows:
■
§ 412.25 Excluded hospital units: Common
requirements.
*
*
*
*
*
(c) The status of a hospital unit may
be changed from not excluded to
excluded or excluded to not excluded at
any time during a cost reporting period,
but only if the hospital notifies the fiscal
intermediary and the CMS Regional
Office in writing of the change at least
30 days before the date of the change,
and maintains the information needed
to accurately determine costs that are or
are not attributable to the hospital unit.
A change in the status of a hospital unit
from not excluded to excluded or
excluded to not excluded that is made
during a cost reporting period must
remain in effect for the rest of that cost
reporting period.
*
*
*
*
*
■ 3. Section 412.433 is added to read as
follows:
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§ 412.433 Procedural requirements under
the IPFQR Program.
(a) Statutory authority. Section
1886(s)(4) of the Act requires the
Secretary to implement a quality
reporting program for inpatient
psychiatric hospitals and psychiatric
units. Under section 1886(s)(4) of the
Act, for an IPF paid under the IPF PPS
that fails to submit data required for the
quality measures selected by the
Secretary in a form and manner and at
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a time specified by the Secretary, we
reduce the otherwise applicable annual
update to the standard Federal rate by
2.0 percentage points with respect to the
applicable fiscal year.
(b) Participation in the IPFQR
Program. To participate in the IPFQR
Program, an IPF (as defined under
§ 412.402) that is paid under the IPF
PPS must:
(1) Register and maintain an account
on the CMS-designated information
system before beginning to report data,
identification of a security official is
necessary to complete such registration;
and
(2) Submit a notice of participation
(NOP).
(c) Withdrawal from the IPFQR
Program. An IPF may withdraw from
the IPFQR Program by changing the
NOP status in the secure portion of the
CMS-designated information system.
The IPF may withdraw at any time up
to and including August 15 before the
beginning of each respective payment
determination year. A withdrawn IPF is
subject to a reduced annual payment
update as specified under paragraph (a)
of this section and is mandatory to
renew participation as specified in
paragraph (b) of this section in order to
participate in any future year of the
IPFQR Program.
(d) Submission of IPFQR Program
data. In general, except as provided in
paragraph (f) of this section, IPFs that
participate in the IPFQR Program must
submit to CMS data on measures
selected under section 1886(s)(4)(D) of
the Act and specified non-measure data
in a form and manner, and at a time
specified by CMS.
(e) Quality measure updates,
retention, and removal. (1) General rule
for updates to quality measures. CMS
uses rulemaking to make substantive
updates to the specifications of
measures used in the IPFQR Program
(2) General rule for the retention of
quality measures. Quality measures
adopted for the IPFQR Program measure
set for a previous payment
determination year are retained for use
in subsequent payment determination
years, except when they are removed,
suspended, or modified as set forth in
paragraph (3) of this section.
(3) Measure removal, suspension, or
modification through the rulemaking
process. CMS will use the regular
rulemaking process to remove, suspend,
or modify quality measures in the
IPFQR Program to allow for public
comment.
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(i) Factors for consideration in
removal or replacement of quality
measures. CMS will weigh whether to
remove or modify measures based on
the following factors:
(A) Factor 1: Measure performance
among IPFs is so high and unvarying
that meaningful distinctions and
improvements in performance can no
longer be made;
(B) Factor 2: Measure does not align
with current clinical guidelines or
practice;
(C) Factor 3: Measure can be replaced
by a more broadly applicable measure
(across settings or populations) or a
measure that is more proximal in time
to desired patient outcomes for the
particular topic;
(D) Factor 4: Measure performance or
improvement does not result in better
patient outcomes;
(E) Factor 5: Measure can be replaced
by a measure that is more strongly
associated with desired patient
outcomes for the particular topic;
(F) Factor 6: Measure collection or
public reporting leads to negative
unintended consequences other than
patient harm;
(G) Factor 7: Measure is not feasible
to implement as specified; and
(H) Factor 8: The costs associated
with a measure outweigh the benefit of
its continued use in the program.
(ii) Retention. CMS may retain a
quality measure that meets one or more
of the measure removal factors
described in paragraph (i) of this
subsection if the continued collection of
data on the quality measure would align
with other CMS and HHS policy goals,
align with other CMS programs, or
support efforts to move IPFs toward
reporting electronic measures.
(f) Extraordinary circumstances
exception. CMS may grant an exception
to one or more data submissions
deadlines and requirements in the event
of extraordinary circumstances beyond
the control of the IPF, such as when an
act of nature affects an entire region or
locale or a systemic problem with one
of CMS’s data collection systems
directly or indirectly affects data
submission. CMS may grant an
exception as follows:
(1) Upon request by the IPF.
(2) At the discretion of CMS. CMS
may grant exceptions to IPFs that have
not requested them when CMS
determines that an extraordinary
circumstance has occurred.
E:\FR\FM\02AUR3.SGM
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(g) Public reporting of IPFQR Program
data. Data that an IPF submits to CMS
for the IPFQR Program will be made
publicly available on a CMS website
after providing the IPF an opportunity
to review the data to be made public.
IPFs will have a period of 30 days to
review and submit corrections to errors
resulting from CMS calculations prior to
the data being made public.
Xavier Becerra,
Secretary, Department of Health and Human
Services.
[FR Doc. 2023–16083 Filed 7–27–23; 4:15 pm]
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Agencies
[Federal Register Volume 88, Number 147 (Wednesday, August 2, 2023)]
[Rules and Regulations]
[Pages 51054-51162]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-16083]
[[Page 51053]]
Vol. 88
Wednesday,
No. 147
August 2, 2023
Part III
Department of Health and Human Services
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Centers for Medicare & Medicaid Services
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42 CFR Part 412
Medicare Program; FY2024 Inpatient Psychiatric Facilities Prospective
Payment System--Rate Update; Final Rule
Federal Register / Vol. 88 , No. 147 / Wednesday, August 2, 2023 /
Rules and Regulations
[[Page 51054]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 412
[CMS-1783-F]
RIN 0938-AV06
Medicare Program; FY 2024 Inpatient Psychiatric Facilities
Prospective Payment System--Rate Update
AGENCY: Centers for Medicare & Medicaid Services (CMS), Department of
Health and Human Services (HHS).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This final rule updates the prospective payment rates, the
outlier threshold, and the wage index for Medicare inpatient hospital
services provided by Inpatient Psychiatric Facilities (IPF), which
include psychiatric hospitals and excluded psychiatric units of an
acute care hospital or critical access hospital. Additionally, this
final rule rebases and revises the IPF market basket to reflect a 2021
base year. These changes will be effective for IPF discharges occurring
during the Fiscal Year (FY) beginning October 1, 2023 through September
30, 2024 (FY 2024). In addition, this final rule discusses quality
measures and reporting requirements under the Inpatient Psychiatric
Facilities Quality Reporting (IPFQR) Program with changes beginning
with the FY 2025 payment determination through changes beginning with
the FY 2028 payment determination.
DATES: These regulations are effective on October 1, 2023.
FOR FURTHER INFORMATION CONTACT: Mollie Knight (410) 786-7948 or
Bridget Dickensheets (410) 786-8670, for information regarding the
market basket update or the labor-related share.
Nick Brock (410) 786-5148 or Theresa Bean (410) 786-2287, for
information regarding the regulatory impact analysis.
Lauren Lowenstein-Turner, (410) 786-4507, for information regarding
the inpatient psychiatric facilities quality reporting program.
SUPPLEMENTARY INFORMATION:
Availability of Certain Tables Exclusively Through the Internet on the
CMS Website
Addendum A to this final rule summarizes the fiscal year (FY) 2024
IPF PPS payment rates, outlier threshold, cost of living adjustment
factors (COLA) for Alaska and Hawaii, national and upper limit cost-to-
charge ratios, and adjustment factors. In addition, Addenda B to this
final rule show the complete listing of ICD-10 Clinical Modification
(CM) and Procedure Coding System (PCS) codes, the FY 2024 IPF PPS
comorbidity adjustment, and electroconvulsive therapy (ECT) procedure
codes. Addenda A and B to this final rule are available online at:
https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/tools.html.
Tables setting forth the FY 2024 Wage Index for Urban Areas Based
on Core Based Statistical Area (CBSA) Labor Market Areas and the FY
2024 Wage Index Based on CBSA Labor Market Areas for Rural Areas are
available exclusively through the internet, on the CMS website at
https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/IPFPPS/WageIndex.html.
I. Executive Summary
A. Purpose
This final rule rebases and revises the market basket for the
Inpatient Psychiatric Facility Prospective Payment System (IPF PPS) to
reflect a 2021 base year, revises the labor-related share, and updates
the prospective payment rates, the outlier threshold, and the wage
index for Medicare inpatient hospital services provided by Inpatient
Psychiatric Facilities (IPFs) for discharges occurring during FY 2024,
(beginning October 1, 2023 through September 30, 2024). This rule also
modifies our regulations to make it easier for hospitals to open new
excluded psychiatric units paid under the IPF PPS. In addition, this
final rule includes a summary of the public comments received to inform
revisions to IPF PPS payments for FY 2025, as required by the
Consolidated Appropriations Act, 2023 (hereafter referred to as CAA,
2023) (Pub. L. 117- 328). Lastly, this final rule discusses quality
measures and reporting requirements under the Inpatient Psychiatric
Facilities Quality Reporting (IPFQR) Program.
B. Summary of the Major Provisions
1. Inpatient Psychiatric Facilities Prospective Payment System (IPF
PPS)
For the IPF PPS, we are finalizing our proposal to--
Modify the regulations to allow the status of a hospital
psychiatric unit to be changed from not excluded to excluded, and
therefore paid under the IPF PPS, at any time during a cost reporting
period if certain requirements are met.
Rebase and revise the IPF market basket to reflect a 2021
base year.
Adjust the 2021-based IPF market basket update (3.5
percent) for economy-wide productivity (0.2 percentage point) as
required by section 1886(s)(2)(A)(i) of the Social Security Act (the
Act), resulting in a final IPF payment rate update of 3.3 percent for
FY 2024.
Make technical rate setting updates: The IPF PPS payment
rates will be adjusted annually for inflation, as well as statutory and
other policy factors.
This rule updates:
++ The IPF PPS Federal per diem base rate from $865.63 to $895.63.
++ The IPF PPS Federal per diem base rate for providers who failed
to report quality data to $878.29.
++ The electroconvulsive therapy (ECT) payment per treatment from
$372.67 to $385.58 .
++ The ECT payment per treatment for providers who failed to report
quality data to $378.12.
++ The labor-related share from 77.4 percent to 78.7 percent.
++ The wage index budget-neutrality factor to 1.0016.
++ The fixed dollar loss threshold amount from $24,630 to $33,470
to maintain estimated outlier payments at 2 percent of total estimated
aggregate IPF PPS payments.
2. Inpatient Psychiatric Facilities Quality Reporting (IPFQR) Program
For the IPFQR Program, we are finalizing our proposals to--
Adopt the Facility Commitment to Health Equity measure
beginning with the FY 2026 payment determination;
Adopt the Screening for Social Drivers of Health measure
beginning with voluntary reporting of calendar year (CY) 2024 data
followed by mandatory reporting of CY 2025 data for the FY 2027 payment
determination;
Adopt the Screen Positive Rate for Social Drivers of
Health measure beginning with voluntary reporting of CY 2024 data
followed by mandatory reporting of CY 2025 data for the FY 2027 payment
determination;
Adopt the Psychiatric Inpatient Experience (PIX) survey to
measure patient experience of care in the IPF setting beginning with
voluntary reporting of CY 2025 data followed by mandatory reporting of
CY 2026 data for the FY 2028 payment determination;
Modify the Coronavirus disease 2019 (COVID-19) Vaccination
Coverage Among Health Care Personnel (HCP) measure to align the measure
with updated measure specifications developed by the Centers for
Disease Control and Prevention (CDC), which
[[Page 51055]]
address refinements reflecting the availability, and FDA authorization,
of Moderna and Pfizer-BioNTech COVID-19 vaccines for use as booster
doses, beginning with fourth quarter CY 2023 data for the FY 2025
payment determination and, following this first single-quarter
reporting period, reporting for the full calendar year beginning with
CY 2024 data for the FY 2026 payment determination;
Remove the following two measures beginning with the FY
2025 payment determination and subsequent years:
++ Patients Discharged on Multiple Antipsychotic Medications with
Appropriate Justification (HBIPS-5); and
++ Tobacco Use Brief Intervention Provided or Offered and Tobacco
Use Brief Intervention Provided (TOB-2/2a) measure;
Adopt a data validation pilot program starting with data
submitted in CY 2025 and continuing until a full data validation
program is proposed and adopted in future rulemaking; and
Codify the IPFQR Program's procedural requirements related
to statutory authority, participation and withdrawal, data submission,
quality measure retention and removal, extraordinary circumstances
exceptions, and public reporting at 42 CFR 412.433 Procedural
requirements under the IPFQR Program.
C. Summary of Impacts
[GRAPHIC] [TIFF OMITTED] TR02AU23.000
II. Background
A. Overview of the Legislative Requirements of the IPF PPS
Section 124 of the Medicare, Medicaid, and State Children's Health
Insurance Program Balanced Budget Refinement Act of 1999 (BBRA) (Pub.
L. 106-113) required the establishment and implementation of an IPF
PPS. Specifically, section 124 of the BBRA mandated that the Secretary
of the Department of Health and Human Services (the Secretary) develop
a per diem payment perspective system (PPS) for inpatient hospital
services furnished in psychiatric hospitals and excluded psychiatric
units including an adequate patient classification system that reflects
the differences in patient resource use and costs among psychiatric
hospitals and excluded psychiatric units. ``Excluded psychiatric unit''
means a psychiatric unit of an acute care hospital or of a Critical
Access Hospital (CAH), which is excluded from payment under the
Inpatient Prospective Payment System (IPPS) or CAH payment system,
respectively. These excluded psychiatric units will be paid under the
IPF PPS.
Section 405(g)(2) of the Medicare Prescription Drug, Improvement,
and Modernization Act of 2003 (MMA) (Pub. L. 108-173) extended the IPF
PPS to psychiatric distinct part units of CAHs.
Sections 3401(f) and 10322 of the Patient Protection and Affordable
Care Act (Pub. L. 111-148) as amended by section 10319(e) of that Act
and by section 1105(d) of the Health Care and Education Reconciliation
Act of 2010 (Pub. L. 111-152) (hereafter referred to jointly as ``the
Affordable Care Act'') added subsection (s) to section 1886 of the
Social Security Act (the Act).
Section 1886(s)(1) of the Act titled, ``Reference to Establishment
and Implementation of System,'' refers to section 124 of the BBRA,
which relates to the establishment of the IPF PPS.
Section 1886(s)(2)(A)(i) of the Act requires the application of the
productivity adjustment described in section 1886(b)(3)(B)(xi)(II) of
the Act to the IPF PPS for the rate year (RY) beginning in 2012 (that
is, a RY that coincides with a FY) and each subsequent RY.
Section 1886(s)(2)(A)(ii) of the Act required the application of an
``other adjustment'' that reduced any update to an IPF PPS base rate by
a percentage point amount specified in section 1886(s)(3) of the Act
for the RY beginning in 2010 through the RY beginning in 2019. As noted
in the FY 2020 IPF PPS final rule, for the RY beginning in 2019,
section 1886(s)(3)(E) of the Act required that the other adjustment
reduction be equal to 0.75 percentage point; that was the final year
the statute required the application of this adjustment. Because FY
2021 was a RY beginning in 2020, FY 2021 was the first-year section
1886(s)(2)(A)(ii) of the Act did not apply since its enactment.
Sections 1886(s)(4)(A) through (D) of the Act require that for RY
2014 and each subsequent RY, IPFs that fail to report required quality
data with respect to such a RY will have their annual update to a
standard Federal rate for discharges reduced by 2.0 percentage points.
This may result in an annual update being less than 0.0 for a RY, and
may result in payment rates for the upcoming RY being less than such
payment rates for the preceding RY. Any reduction for failure to report
required quality data will apply only to the RY involved, and the
Secretary will not consider such reduction in computing the payment
amount for a subsequent RY. Section 4125 of division FF, title IV,
subtitle C, the CAA, 2023 requires that not later than FY 2028 each IPF
will submit data through the use of a standardized assessment
instrument which includes data on functional status; cognitive
function; special services treatments, and interventions for
psychiatric conditions; impairments; and other categories deemed
appropriate. In addition, section 4125 of the CAA, 2023 requires that a
patients' perspective of care quality measure be added to the IPFQR
Program not later than for FY 2031. Information regarding the newly
[[Page 51056]]
adopted Psychiatric Inpatient Experience (PIX) survey measure is
provided in section VI.D.5 of this final rule.
Section 4125 of the CAA, 2023 also requires revisions to the
Medicare prospective payment system (PPS) for psychiatric hospitals and
psychiatric units. Specifically, section 4125(a) of the CAA, 2023
amends section 1886(s) of the Act by adding a new paragraph (5) that
requires the Secretary to collect data and information beginning no
later than October 1, 2023, as the Secretary determines appropriate, to
inform revisions to IPF PPS payments. In addition, the Secretary is
required to implement revisions to the methodology for determining the
payment rates under the IPF PPS for FY 2025 as the Secretary determines
appropriate.
To implement and periodically update the IPF PPS, we have published
various proposed and final rules and notices in the Federal Register.
For more information regarding these documents, see the CMS website at
https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/?redirect=/InpatientPsychFacilPPS/.
B. Overview of the IPF PPS
On November 15, 2004, we published the IPF PPS final rule in the
Federal Register (69 FR 66922). The November 2004 IPF PPS final rule
established the IPF PPS, as required by section 124 of the BBRA and
codified at 42 CFR part 412, subpart N. The November 2004 IPF PPS final
rule set forth the Federal per diem base rate for the implementation
year (the 18-month period from January 1, 2005 through June 30, 2006),
and provided payment for the inpatient operating and capital costs to
IPFs for covered psychiatric services they furnish (that is, routine,
ancillary, and capital costs, but not costs of approved educational
activities, bad debts, and other services or items that are outside the
scope of the IPF PPS). Covered psychiatric services include services
for which benefits are provided under the fee-for-service Part A
(Hospital Insurance Program) of the Medicare program.
The IPF PPS established the Federal per diem base rate for each
patient day in an IPF derived from the national average daily routine
operating, ancillary, and capital costs in IPFs in FY 2002. The average
per diem cost was updated to the midpoint of the first year under the
IPF PPS, standardized to account for the overall positive effects of
the IPF PPS payment adjustments, and adjusted for budget-neutrality.
The Federal per diem payment under the IPF PPS is comprised of the
Federal per diem base rate described previously and certain patient-
and facility-level payment adjustments for characteristics that were
found in the regression analysis to be associated with statistically
significant per diem cost differences; with statistical significance
defined as p less than 0.05. A complete discussion of the regression
analysis that established the IPF PPS adjustment factors can be found
in the November 2004 IPF PPS final rule (69 FR 66933 through 66936).
The patient-level adjustments include age, Diagnosis-Related Group
(DRG) assignment, and comorbidities, as well as adjustments to reflect
higher per diem costs at the beginning of a patient's IPF stay and
lower costs for later days of the stay. Facility-level adjustments
include adjustments for the IPF's wage index, rural location, teaching
status, a cost-of-living adjustment for IPFs located in Alaska and
Hawaii, and an adjustment for the presence of a qualifying emergency
department (ED).
The IPF PPS has additional payment policies for outlier cases,
interrupted stays, and a per treatment payment for patients who undergo
ECT. During the IPF PPS mandatory 3-year transition period, stop-loss
payments were also provided; however, since the transition ended as of
January 1, 2008, these payments are no longer available.
C. Annual Requirements for Updating the IPF PPS
Section 124 of the BBRA did not specify an annual rate update
strategy for the IPF PPS and was broadly written to give the Secretary
discretion in establishing an update methodology. In the November 2004
IPF PPS final rule (69 FR 66922), we implemented the IPF PPS using the
following update strategy:
Calculate the final Federal per diem base rate to be
budget-neutral for the 18-month period of January 1, 2005 through June
30, 2006.
Use a July 1 through June 30 annual update cycle.
Allow the IPF PPS first update to be effective for
discharges on or after July 1, 2006 through June 30, 2007.
In developing the IPF PPS, and to ensure that the IPF PPS can
account adequately for each IPF's case-mix, we performed an extensive
regression analysis of the relationship between the per diem costs and
certain patient and facility characteristics to determine those
characteristics associated with statistically significant cost
differences on a per diem basis. That regression analysis is described
in detail in our November 28, 2003 IPF PPS proposed rule (68 FR 66923;
66928 through 66933) and our November 15, 2004 IPF PPS final rule (69
FR 66933 through 66960). For characteristics with statistically
significant cost differences, we used the regression coefficients of
those variables to determine the size of the corresponding payment
adjustments.
In the November 2004 IPF PPS final rule, we explained the reasons
for delaying an update to the adjustment factors, derived from the
regression analysis, including waiting until we have IPF PPS data that
yields as much information as possible regarding the patient-level
characteristics of the population that each IPF serves. We indicated
that we did not intend to update the regression analysis and the
patient-level and facility-level adjustments until we complete that
analysis. Until that analysis is complete, we stated our intention to
publish a notice in the Federal Register each spring to update the IPF
PPS (69 FR 66966).
On May 6, 2011, we published a final rule in the Federal Register
titled, ``Inpatient Psychiatric Facilities Prospective Payment System--
Update for Rate Year Beginning July 1, 2011 (RY 2012)'' (76 FR 26432),
which changed the payment rate update period to a RY that coincides
with a FY update. Therefore, final rules are now published in the
Federal Register in the summer to be effective on October 1st. When
proposing changes in IPF payment policy, a proposed rule would be
issued in the spring and the final rule in the summer to be effective
on October 1st. For a detailed list of updates to the IPF PPS, we refer
readers to our regulations at 42 CFR 412.428.
The most recent IPF PPS annual update was published in a final rule
on July 29, 2022 in the Federal Register titled, ``Medicare Program; FY
2023 Inpatient Psychiatric Facilities Prospective Payment System--Rate
Update and Quality Reporting--Request for Information'' (87 FR 46846),
which updated the IPF PPS payment rates for FY 2023. That final rule
updated the IPF PPS Federal per diem base rates that were published in
the FY 2022 IPF PPS Rate Update final rule (86 FR 42608) in accordance
with our established policies.
III. Analysis of and Responses to Public Comments
We received 2,506 public comments that pertain to proposed IPF PPS
payment policies, requests for information, and the proposed updates to
the IPFQR Program. Comments were
[[Page 51057]]
from Inpatient Psychiatric Facilities, health systems, national and
state level provider and patient advocacy organizations, the Medicare
Payment Advisory Commission (MedPAC), and individuals. We reviewed each
comment and grouped related comments, after which we placed them in
categories based on subject matter or section(s) of the regulation
affected. Summaries of the public comments received and our responses
to those comments are provided in the appropriate sections in the
preamble of this final rule.
IV. Provisions of the FY 2024 IPF PPS Final Rule and Responses to
Comments
A. Rebasing and Revising of the Market Basket for the IPF PPS
1. Background
Originally, the input price index used to develop the IPF PPS was
the Excluded Hospital with Capital market basket. This market basket
was based on 1997 Medicare cost reports for Medicare-participating
inpatient rehabilitation facilities (IRFs), IPFs, long-term care
hospitals (LTCHs), cancer hospitals, and children's hospitals. Although
``market basket'' technically describes the mix of goods and services
used in providing health care at a given point in time, this term is
also commonly used to denote the input price index (that is, cost
category weights and price proxies) derived from that market basket.
Accordingly, the term ``market basket,'' as used in this document,
refers to an input price index.
Since the IPF PPS inception, the market basket used to update IPF
PPS payments has been rebased and revised to reflect more recent data
on IPF cost structures. We last rebased and revised the market basket
applicable to the IPF PPS in the FY 2020 IPF PPS final rule (84 FR
38426 through 38447), where we adopted a 2016-based IPF market basket.
The 2016-based IPF market basket used Medicare cost report data for
both Medicare-participating freestanding psychiatric hospitals and
hospital-based psychiatric units. References to the historical market
baskets used to update IPF PPS payments are listed in the FY 2016 IPF
PPS final rule (80 FR 46656). For the FY 2024 IPF PPS proposed rule, we
proposed to rebase and revise the IPF market basket to reflect a 2021
base year.
2. Overview of the 2021-Based IPF Market Basket
The 2021-based IPF market basket is a fixed-weight, Laspeyres-type
price index. A Laspeyres price index measures the change in price, over
time, of the same mix of goods and services purchased in the base
period. Any changes in the quantity or mix of goods and services (that
is, intensity) purchased over time relative to a base period are not
measured.
The index itself is constructed in three steps. First, a base
period is selected (in the proposed rule, we proposed to use 2021 as
the base period) and total base period costs are estimated for a set of
mutually exclusive and exhaustive cost categories. Each category is
calculated as a proportion of total costs. These proportions are called
cost weights. Second, each cost category is matched to an appropriate
price or wage variable, referred to as a price proxy. In nearly every
instance, these price proxies are derived from publicly available
statistical series that are published on a consistent schedule
(preferably at least on a quarterly basis). Finally, the cost weight
for each cost category is multiplied by the level of its respective
price proxy. The sum of these products (that is, the cost weights
multiplied by their price index levels) for all cost categories yields
the composite index level of the market basket in a given period.
Repeating this step for other periods produces a series of market
basket levels over time. Dividing an index level for a given period by
an index level for an earlier period produces a rate of growth in the
input price index over that timeframe.
As noted, the market basket is described as a fixed-weight index
because it represents the change in price over time of a constant mix
(quantity and intensity) of goods and services needed to provide IPF
services. The effects on total costs resulting from changes in the mix
of goods and services purchased subsequent to the base period are not
measured. For example, an IPF hiring more nurses after the base period
to accommodate the needs of patients will increase the volume of goods
and services purchased by the IPF but will not be factored into the
price change measured by a fixed-weight IPF market basket. Only when
the index is rebased will changes in the quantity and intensity be
captured, with those changes being reflected in the cost weights.
Therefore, we rebase the market basket periodically so that the cost
weights reflect recent changes in the mix of goods and services that
IPFs purchase to furnish inpatient care between base periods.
3. Rebasing and Revising of the IPF Market Basket
As discussed in the FY 2020 IPF PPS final rule (84 FR 38426 through
38447), the 2016-based IPF market basket reflects the Medicare cost
reports for both freestanding and hospital-based IPFs. Beginning with
FY 2024, we proposed to rebase and revise the IPF market basket to a
2021 base year reflecting the 2021 Medicare cost report data submitted
by both freestanding and hospital-based IPFs. We provide a detailed
description of our proposed methodology used to develop the 2021-based
IPF market basket below. This proposed methodology is generally similar
to the methodology used to develop the 2016-based IPF market basket. We
solicited public comment on our proposed methodology for developing the
2021-based IPF market basket.
Comment: Several commenters supported CMS's proposal to rebase and
revise the market basket to reflect more recent data, noting that the
changes in the cost weights were consistent with their expectations or
experience. One commenter, however, proposed that CMS wait to rebase
the IPF market basket until FY 2022 data is available. The commenter
stated that, due to the increased demand for hospital care during the
initial year following the outbreak of COVID-19 in the United States,
they assume that a base year of FY 2021 would not necessarily reflect
costs in FY 2024. Though inflation was particularly high during FY
2021, the commenter noted that FY 2022 would be further removed from
the initial outbreak of COVID-19 in the United States and the massive
changes in healthcare that occurred during that time. Similarly, one
commenter supported the proposal to rebase but recommended CMS plan to
rebase and revise the market basket and labor-related share to reflect
a 2023 base year to fully incorporate the cost structures from the
Public Health Emergency (PHE) as well as the evolving hospital
workforce shortage.
Response: We appreciate the commenters' support regarding the
proposed IPF market basket. For the proposed rebasing and revising, we
used the most current and complete set of Medicare cost report data
(2021) at the time of rulemaking to determine the major base year cost
weights (Wages and Salaries, Employee Benefits, Contract Labor,
Professional Liability Insurance, Pharmaceuticals, Home Office/Related
Organization Contract Labor, and Capital).
As stated in the FY 2024 IPF PPS proposed rule (88 FR 21241), many
commenters expressed concern in response to the FY 2023 IPF PPS
proposed rule, in which we did not propose to rebase the IPF market
basket.
[[Page 51058]]
The commenters stated at that time that the 2016-based IPF market
basket did not reflect the current costs of IPFs, particularly the use
of contract labor. Therefore, based on the typical timeframe for
rebasing the market baskets and in response to commenters' concerns
expressed in FY 2023 IPF rulemaking, we proposed to rebase and revise
the IPF market basket for FY 2024. We understand the commenters'
concerns that the impact of the PHE may have resulted in increased
costs compared to 2016. However, we believe it is appropriate to rebase
the market basket regularly and to reflect more recent IPF cost
structures. It has been our longstanding practice to rebase the IPF
market basket (as well as other CMS market baskets) on a regular basis
to ensure it reflects a more up-to-date input cost structure of IPFs so
that the price change in the market basket best reflects input prices
faced by IPFs. Because complete 2022 IPF Medicare cost report data is
currently unavailable, we believe it is more appropriate to update the
base year cost weights to 2021 to reflect changes over this period
rather than to delay the rebasing for another year or two in order to
use 2022 or 2023 Medicare cost report data as suggested by the
commenter. We regularly rebase every 4 to 5 years because more recent
data is typically more reflective of IPF cost structures. Therefore, we
are using the most recent cost report data we have, which is 2021 cost
report data, as it is more reflective of IPF cost structures than 2016
data. For example, the 2021-based IPF market basket reflects the higher
compensation cost weight (as compared to the 2016-based IPF market
basket) as a result of an increase in the contract labor cost weight
(calculated using the 2021 Medicare cost report data) as noted by the
commenters in response to the FY 2023 IPF proposed rule (87 FR 46849).
Additionally, we will continue to monitor the Medicare cost report data
to assess whether a more frequent rebasing of the IPF market basket is
appropriate through future notice and comment rulemaking.
Final Decision: We are finalizing our proposal to rebase the IPF
market basket to reflect a 2021 base year for FY 2024.
We provide a summary of the more detailed public comments received
on our proposed methodology for developing the 2021-based IPF market
basket and our responses in the following sections.
a. Development of Cost Categories and Weights for the 2021-Based IPF
Market Basket
(1) Use of Medicare Cost Report Data
We proposed a 2021-based IPF market basket that consists of seven
major cost categories and a residual derived from the 2021 Medicare
cost reports (CMS Form 2552-10, OMB No. 0938-0050) for freestanding and
hospital-based IPFs. The seven major cost categories are Wages and
Salaries, Employee Benefits, Contract Labor, Pharmaceuticals,
Professional Liability Insurance (PLI), Home Office/Related
Organization Contract Labor, and Capital. The cost reports include
providers whose cost reporting period began on or after October 1, 2020
and before October 1, 2021. As noted previously, the current IPF market
basket is based on 2016 Medicare cost reports and therefore, reflects
the 2016 cost structure for IPFs. As described in the FY 2023 IPF PPS
final rule (87 FR 46849), we received comments on the FY 2023 IPF PPS
proposed rule (87 FR 19418 through 19419) where stakeholders expressed
concern that the proposed market basket update inadequately reflected
the input price inflation experienced by IPFs, particularly as a result
of the COVID-19 PHE. These commenters stated that the PHE, along with
inflation, has significantly driven up operating costs. Specifically,
some commenters noted changes to labor markets that led to the use of
more contract labor, a trend that we verified in analyzing the Medicare
cost report data through 2021. Therefore, we believe it is appropriate
to incorporate more recent data to reflect updated cost structures for
IPFs, and so we proposed to use 2021 as the base year, because we
believe that the Medicare cost reports for this year represent the most
recent complete set of Medicare cost report data available for
developing the proposed IPF market basket at the time of this
rulemaking. Given the potential impact of the PHE on the Medicare cost
report data, we will continue to monitor these data going forward, and
any changes to the IPF market basket will be proposed in future
rulemaking.
Similar to the Medicare cost report data used to develop the 2016-
based IPF market basket, the Medicare cost report data for 2021 show
large differences between some providers' Medicare length of stay (LOS)
and total facility LOS. Our goal has always been to measure cost
weights that are reflective of case mix and practice patterns
associated with providing services to Medicare beneficiaries.
Therefore, we proposed to limit our selection of Medicare cost reports
used in the 2021-based IPF market basket to those facilities that had a
Medicare LOS within a comparable range of their total facility average
LOS. The Medicare average LOS for freestanding IPFs is calculated from
data reported on line 14 of Worksheet S-3, part I. The Medicare average
LOS for hospital-based IPFs is calculated from data reported on line 16
of Worksheet S-3, part I. To derive the 2021-based IPF market basket,
for those IPFs with an average facility LOS of greater than or equal to
15 days, we proposed to include IPFs where the Medicare LOS is within
50 percent (higher or lower) of the average facility LOS. For those
IPFs whose average facility LOS is less than 15 days, we proposed to
include IPFs where the Medicare LOS is within 95 percent (higher or
lower) of the facility LOS. We proposed to apply this LOS edit to the
data for IPFs to exclude providers that serve a population whose LOS
will indicate that the patients served are not consistent with a LOS of
a typical Medicare patient. This is the same LOS edit applied to the
2016-based IPF market basket.
Applying these trims to the approximate 1,370 total cost reports
(freestanding and hospital-based) resulted in roughly 1,250 IPF
Medicare cost reports with an average Medicare LOS of 13 days, average
facility LOS of 10 days, and Medicare utilization (as measured by
Medicare inpatient IPF days as a percentage of total facility days) of
16 percent. Providers excluded from the 2021-based IPF market basket
(about 120 Medicare cost reports) had an average Medicare LOS of 21
days, average facility LOS of 41 days, and a Medicare utilization of 3
percent. Of those excluded, about 62 percent of these were freestanding
providers; on the other hand, freestanding providers represent about 38
percent of all IPFs. We note that 70 percent of those excluded from the
2016-based IPF market basket using this LOS edit were freestanding
providers.
We then proposed to use the cost reports for IPFs that met this
requirement to calculate the costs for the seven major cost categories
(Wages and Salaries, Employee Benefits, Contract Labor, Professional
Liability Insurance, Pharmaceuticals, Home Office/Related Organization
Contract Labor, and Capital) for the market basket. These are the same
categories used for the 2016-based IPF market basket. Also, as
described in section IV.A.3.a.(4) of this final rule, and as done for
the 2016-based IPF market basket, we proposed to use the Medicare cost
report data to calculate the detailed
[[Page 51059]]
capital cost weights for the Depreciation, Interest, Lease, and Other
Capital-related cost categories. We also proposed to rename the Home
Office Contract Labor cost category to the Home Office/Related
Organization Contract Labor cost category to be more consistent with
the Medicare cost report instructions.
Similar to the 2016-based IPF market basket major cost weights, for
the majority of the 2021-based IPF market basket cost weights, we
proposed to divide the costs for each cost category by total Medicare
allowable costs (routine, ancillary and capital)--costs that are
eligible for payment through the IPF PPS (we noted that we use total
facility medical care costs as the denominator to derive both the PLI
and Home Office/Related Organization Contract Labor cost weights). We
next describe our proposed methodology for deriving the cost levels
used to derive the 2021-based IPF market basket.
(a) Total Medicare Allowable Costs
For freestanding IPFs, we proposed that total Medicare allowable
costs would be equal to the sum of total costs for the Medicare
allowable cost centers as reported on Worksheet B, part I, column 26,
lines 30 through 35, 50 through 76 (excluding 52 and 75), 90 through
91, and 93.
For hospital-based IPFs, we proposed that total Medicare allowable
costs would be equal to the total costs for the IPF inpatient unit
after the allocation of overhead costs (Worksheet B, part I, column 26,
line 40) and a proportion of total ancillary costs reported on
Worksheet B, part I, column 26, lines 50 through 76 (excluding 52 and
75), 90 through 91, and 93.
We proposed to calculate total ancillary costs attributable to the
hospital-based IPF by first deriving an ``IPF ancillary ratio'' for
each ancillary cost center. The IPF ancillary ratio is defined as the
ratio of IPF Medicare ancillary costs for the cost center (as reported
on Worksheet D-3, column 3 for hospital-based IPFs) to total Medicare
ancillary costs for the cost center (equal to the sum of Worksheet D-3,
column 3 for all relevant PPSs [that is, IPPS, IRF, IPF and skilled
nursing facility (SNF)]). For example, if hospital-based IPF Medicare
laboratory costs represent about 2 percent of the total Medicare
laboratory costs for the entire facility, then the IPF ancillary ratio
for laboratory costs would be 2 percent. We believe it is appropriate
to use only a portion of the ancillary costs in the market basket cost
weight calculations since the hospital-based IPF only utilizes a
portion of the facility's ancillary services. We believe the ratio of
reported IPF Medicare costs to reported total Medicare costs provides a
reasonable estimate of the ancillary services utilized, and costs
incurred, by the hospital-based IPF. We proposed that this IPF
ancillary ratio for each cost center is also used to calculate Wages
and Salaries and Capital costs as described below.
Then, for each ancillary cost center, we proposed to multiply the
IPF ancillary ratio for the given cost center by the total facility
ancillary costs for that specific cost center (as reported on Worksheet
B, part I, column 26) to derive IPF ancillary costs. For example, the 2
percent IPF ancillary ratio for laboratory cost center would be
multiplied by the total ancillary costs for laboratory (Worksheet B,
part I, column 26, line 60). The IPF ancillary costs for each cost
center are then added to total costs for the IPF inpatient unit after
the allocation of overhead costs (Worksheet B, part I, column 26, line
40) to derive total Medicare allowable costs.
We proposed to use these methods to derive levels of total Medicare
allowable costs for IPF providers. This is the same methodology used
for the 2016-based IPF market basket. We proposed that these total
Medicare allowable costs for the IPF will be the denominator for the
cost weight calculations for the Wages and Salaries, Employee Benefits,
Contract Labor, Pharmaceuticals, and Capital cost weights. With this
work complete, we then set about deriving cost levels for the seven
major cost categories and then derive a residual cost weight reflecting
all other costs not classified.
(b) Wages and Salaries Costs
For freestanding IPFs, we proposed to derive Wages and Salaries
costs as the sum of routine inpatient salaries (Worksheet A, column 1,
lines 30 through 35), ancillary salaries (Worksheet A, column 1, lines
50 through 76 (excluding 52 and 75), 90 through 91, and 93), and a
proportion of overhead (or general service cost centers in the Medicare
cost reports) salaries. Since overhead salary costs are attributable to
the entire IPF, we only include the proportion attributable to the
Medicare allowable cost centers. We proposed to estimate the proportion
of overhead salaries that are attributed to Medicare allowable costs
centers by multiplying the ratio of Medicare allowable area salaries
(Worksheet A, column 1, lines 30 through 35, 50 through 76 (excluding
52 and 75), 90 through 91, and 93) to total non-overhead salaries
(Worksheet A, column 1, line 200 less Worksheet A, column 1, lines 4
through 18) times total overhead salaries (Worksheet A, column 1, lines
4 through 18). This is a similar methodology as used in the 2016-based
IPF market basket.
For hospital-based IPFs, we proposed to derive Wages and Salaries
costs as the sum of the following salaries attributable to the
hospital-based IPF: Inpatient routine salary costs (Worksheet A, column
1, line 40); overhead salary costs; ancillary salary costs; and a
portion of overhead salary costs attributable to the ancillary
departments.
(i) Overhead Salary Costs
We proposed to calculate the portion of overhead salary cost
attributable to hospital-based IPFs by first calculating an IPF
overhead salary ratio, which is equal to the ratio of total facility
overhead salaries (as reported on Worksheet A, column 1, lines 4-18) to
total facility noncapital overhead costs (as reported on Worksheet A,
column 1 and 2, lines 4-18). We then proposed to multiply this IPF
overhead salary ratio by total noncapital overhead costs (sum of
Worksheet B, part I, columns 4 through 18, line 40, less Worksheet B,
part II, columns 4 through 18, line 40). This methodology assumes the
proportion of total costs related to salaries for the overhead cost
center is similar for all inpatient units (that is, acute inpatient or
inpatient psychiatric).
(ii) Ancillary Salary Costs
We proposed to calculate hospital-based IPF ancillary salary costs
for a specific cost center (Worksheet A, column 1, lines 50 through 76
(excluding 52 and 75), 90 through 91, and 93) as salary costs from
Worksheet A, column 1, multiplied by the IPF ancillary ratio for each
cost center as described in section IV.A.3.a.(1)(a) of this final rule.
The sum of these costs represents hospital-based IPF ancillary salary
costs.
(iii) Overhead Salary Costs for Ancillary Cost Centers
We proposed to calculate the portion of overhead salaries
attributable to each ancillary department (lines 50 through 76
(excluding 52 and 75), 90 through 91, and 93) by first calculating
total noncapital overhead cost attributable to each specific ancillary
department (sum of Worksheet B, part I, columns 4-18, less Worksheet B,
part II, column 26). We then identify the portion of these total
noncapital overhead cost for each ancillary department that is
attributable to the hospital-based IPF by multiplying these costs by
the IPF ancillary ratio as described in section IV.A.3.a.(1)(a) of
[[Page 51060]]
this final rule. We then sum these estimated IPF Medicare allowable
noncapital overhead costs for all ancillary departments (cost centers
50 through 76, 90 through 91, and 93). Finally, we then identify the
portion of these IPF Medicare allowable noncapital overhead cost that
are attributable to Wages and Salaries by multiplying these costs by
the IPF overhead salary ratio as described in section
IV.A.3.a.(1)(b)(i) of this final rule. This is the same methodology
used to derive the 2016-based IPF market basket.
(c) Employee Benefits Costs
Effective with the implementation of CMS Form 2552-10, we began
collecting Employee Benefits and Contract Labor data on Worksheet S-3,
part V.
For the 2021 Medicare cost report data, the majority of IPF
providers did not report data on Worksheet S-3, part V. Two percent of
freestanding IPFs and roughly 48 percent of hospital-based IPFs
reported Employee Benefits data on Worksheet S-3, part V. Two percent
of freestanding IPFs and roughly 13 percent of hospital-based IPFs
reported Contract Labor data on Worksheet S-3, part V. We continue to
encourage all providers to report these data on the Medicare cost
report.
For freestanding IPFs, we proposed that Employee Benefits cost
would be equal to the data reported on Worksheet S-3, part V, column 2,
line 2. We note that while not required to do so, freestanding IPFs
also may report Employee Benefits data on Worksheet S-3, part II, which
is applicable to only IPPS providers. Similar to the method for the
2016-based IPF market basket, for those freestanding IPFs that report
Worksheet S-3, part II, data, but not Worksheet S-3, part V, we
proposed to use the sum of Worksheet S-3, part II, lines 17, 18, 20,
and 22, to derive Employee Benefits costs.
For hospital-based IPFs, we proposed to calculate total benefit
cost as the sum of inpatient unit benefit cost, a portion of ancillary
departments benefit costs, and a portion of overhead benefits
attributable to both the routine inpatient unit and the ancillary
departments. For those hospital-based IPFs that report Worksheet S-3,
part V data, we proposed inpatient unit benefit costs be equal to
Worksheet S-3, part V, column 2, line 3. Given the limited reporting on
Worksheet S-3, part V, we proposed that for those hospital-based IPFs
that do not report these data, we calculate inpatient unit benefits
cost using a portion of benefits cost reported for Excluded areas on
Worksheet S-3, part II. We proposed to calculate the ratio of inpatient
unit salaries (Worksheet A, column 1, line 40) to total excluded area
salaries (sum of Worksheet A, column 1, lines 20, 23, 40 through 42,
44, 45, 46, 94, 95, 98 through 101, 105 through 112, 114, 115 through
117, 190 through 194). We then proposed to apply this ratio to Excluded
area benefits (Worksheet S-3, part II, column 4, line 19) to derive
inpatient unit benefits cost for those providers that do not report
benefit costs on Worksheet S-3, part V.
We proposed the ancillary departments benefits and overhead
benefits (attributable to both the inpatient unit and ancillary
departments) costs are derived by first calculating the sum of
hospital-based IPF overhead salaries as described in section
IV.A.3.a.(1)(b)(i) of this final rule, hospital-based IPF ancillary
salaries as described in section IV.A.3.a.(1)(b)(ii) of this final rule
and hospital-based IPF overhead salaries for ancillary cost centers as
described in section IV.A.3.a.(1)(b)(iii) of this final rule. This sum
is then multiplied by the ratio of total facility benefits to total
facility salaries, where total facility benefits is equal to the sum of
Worksheet S- 3, part II, column 4, lines 17-25, and total facility
salaries is equal to Worksheet S-3, part II, column 4, line 1.
(d) Contract Labor Costs
Contract Labor costs are primarily associated with direct patient
care services. Contract labor costs for other services such as
accounting, billing, and legal are calculated separately using other
government data sources as described in section IV.A.3.a.(3) of this
final rule. To derive contract labor costs using Worksheet S-3, part V,
data for freestanding IPFs, we proposed Contract Labor costs be equal
to Worksheet S-3, part V, column 1, line 2. As we noted for Employee
Benefits, freestanding IPFs also may report Contract Labor data on
Worksheet S-3, part II, which is applicable to only IPPS providers. For
those freestanding IPFs that report Worksheet S-3, part II data, but
not Worksheet S-3, part V, we proposed to use the sum of Worksheet S-3,
part II, column 4, lines 11 and 13, to derive Contract Labor costs.
For hospital-based IPFs, we proposed that Contract Labor costs be
equal to Worksheet S- 3, part V, column 1, line 3. Reporting of this
data continues to be somewhat limited; therefore, we continue to
encourage all providers to report these data on the Medicare cost
report. Given the limited reporting on Worksheet S-3, part V, we
proposed that for those hospital-based IPFs that do not report these
data, we calculate Contract Labor costs using a portion of contract
labor costs reported on Worksheet S-3, part II. We proposed to
calculate the ratio of contract labor costs (Worksheet S-3, part II,
column 4, lines 11 and 13) to PPS salaries (Worksheet S-3, part II,
column 4, line 1 less the sum of Worksheet S-3, part II, column 4,
lines 3, 401, 5, 6, 7, 701, 8, 9, 10 less Worksheet A, column 1, line
20 and 23). We then proposed to apply this ratio to total inpatient
routine salary costs (Worksheet A, column 1, line 40) to derive
contract labor costs for those providers that do not report contract
labor costs on Worksheet S-3, part V.
(e) Pharmaceuticals Costs
For freestanding IPFs, we proposed to calculate pharmaceuticals
costs using non-salary costs reported on Worksheet A, column 7, less
Worksheet A, column 1, for the pharmacy cost center (line 15) and drugs
charged to patients cost center (line 73).
For hospital-based IPFs, we proposed to calculate pharmaceuticals
costs as the sum of a portion of the non-salary pharmacy costs and a
portion of the non-salary drugs charged to patient costs reported for
the total facility. We proposed that non-salary pharmacy costs
attributable to the hospital-based IPF would be calculated by
multiplying total pharmacy costs attributable to the hospital-based IPF
(as reported on Worksheet B, part I, column 15, line 40) by the ratio
of total non-salary pharmacy costs (Worksheet A, column 2, line 15) to
total pharmacy costs (sum of Worksheet A, columns 1 and 2 for line 15)
for the total facility. We proposed that non-salary drugs charged to
patient costs attributable to the hospital-based IPF would be
calculated by multiplying total non-salary drugs charged to patient
costs (Worksheet B, part I, column 0, line 73 plus Worksheet B, part I,
column 15, line 73 less Worksheet A, column 1, line 73) for the total
facility by the ratio of Medicare drugs charged to patient ancillary
costs for the IPF unit (as reported on Worksheet D-3 for hospital-based
IPFs, column 3, line 73) to total Medicare drugs charged to patient
ancillary costs for the total facility (equal to the sum of Worksheet
D-3, column 3, line 73 for all relevant PPS [that is, IPPS, IRF, IPF
and SNF]).
(f) Professional Liability Insurance Costs
For freestanding and hospital-based IPFs, we proposed that
Professional Liability Insurance (PLI) costs (often referred to as
malpractice costs) would be equal to premiums, paid losses and self-
insurance costs reported on Worksheet S-2, columns 1 through 3, line
118--the same data used for the
[[Page 51061]]
2016-based IPF market basket. For hospital-based IPFs, we proposed to
assume that the PLI weight for the total facility is similar to the
hospital-based IPF unit since the only data reported on this worksheet
is for the entire facility, as we currently have no means to identify
the proportion of total PLI costs that are only attributable to the
hospital-based IPF. However, when we derive the cost weight for PLI for
both hospital-based and freestanding IPFs, we use the total facility
medical care costs as the denominator as opposed to total Medicare
allowable costs. For freestanding IPFs and hospital-based IPFs, we
proposed to derive total facility medical care costs as the sum of
total costs (Worksheet B, part I, column 26, line 202) less non-
reimbursable costs (Worksheet B, part I, column 26, lines 190 through
201). Our assumption is that the same proportion of expenses are used
among each unit of the hospital.
(g) Home Office/Related Organization Contract Labor Costs
For hospital-based IPFs, we proposed to calculate the Home Office/
Related Organization Contract Labor costs using data reported on
Worksheet S-3, part II, column 4, lines 1401, 1402, 2550, and 2551.
Similar to the PLI costs, these costs are for the entire facility.
Therefore, when we derive the cost weight for home office/related
organization contract labor costs, we use the total facility medical
care costs as the denominator (reflecting the total facility costs
(Worksheet B, part I, column 26, line 202) less the nonreimbursable
costs reported on lines 190 through 201).
(h) Capital Costs
For freestanding IPFs, we proposed that capital costs would be
equal to Medicare allowable capital costs as reported on Worksheet B,
part II, column 26, lines 30 through 35, 50 through 76 (excluding 52
and 75), 90 through 91, and 93.
For hospital-based IPFs, we proposed that capital costs would be
equal to IPF inpatient capital costs (as reported on Worksheet B, part
II, column 26, line 40) and a portion of IPF ancillary capital costs.
We calculate the portion of ancillary capital costs attributable to the
hospital-based IPF for a given cost center by multiplying total
facility ancillary capital costs for the specific ancillary cost center
(as reported on Worksheet B, part II, column 26) by the IPF ancillary
ratio as described in section IV.A.3.a.(1)(a) of this final rule.
(2) Final Major Cost Category Computation
After we derive costs for each of the major cost categories and
total Medicare allowable costs for each provider using the Medicare
cost report data as previously described, we proposed to address data
outliers using the following steps. First, for the Wages and Salaries,
Employee Benefits, Contract Labor, Pharmaceuticals, and Capital cost
weights, we first divide the costs for each of these five categories by
total Medicare allowable costs calculated for the provider to obtain
cost weights for the universe of IPF providers. We then proposed to
trim the data to remove outliers (a standard statistical process) by:
(1) requiring that major expenses (such as Wages and Salaries costs)
and total Medicare allowable operating costs be greater than zero; and
(2) excluding the top and bottom 5 percent of the major cost weight
(for example, Wages and Salaries costs as a percent of total Medicare
allowable operating costs). We note that missing values are assumed to
be zero consistent with the methodology for how missing values were
treated in the 2016-based IPF market basket. After these outliers have
been excluded, we sum the costs for each category across all remaining
providers. We then divide this by the sum of total Medicare allowable
costs across all remaining providers to obtain a cost weight for the
2021-based IPF market basket for the given category.
The proposed trimming methodology for the Home Office/Related
Organization Contract Labor and PLI cost weights are slightly different
than the proposed trimming methodology for the other five cost
categories as described above. For these cost weights, since we are
using total facility medical care costs rather than Medicare allowable
costs associated with IPF services, we proposed to trim the
freestanding and hospital-based IPF cost weights separately.
For the PLI cost weight, for each of the providers, we first divide
the PLI costs by total facility medical care costs to obtain a PLI cost
weight for the universe of IPF providers. We then proposed to trim the
data to remove outliers by: (1) requiring that PLI costs are greater
than zero and are less than total facility medical care costs; and (2)
excluding the top and bottom 5 percent of the major cost weight
trimming freestanding and hospital-based providers separately. After
removing these outliers, we are left with a trimmed data set for both
freestanding and hospital-based providers. We proposed to separately
sum the costs for each category (freestanding and hospital-based)
across all remaining providers. We next divide this by the sum of total
facility medical care costs across all remaining providers to obtain
both a freestanding cost weight and hospital-based cost weight. Lastly,
we proposed to weight these two cost weights together using the
Medicare allowable costs from the sample of freestanding and hospital-
based IPFs that passed the PLI trim (63 percent for hospital-based and
37 percent for freestanding IPFs) to derive a PLI cost weight for the
2021-based IPF market basket.
For the Home Office/Related Organization Contract Labor cost
weight, for each of the providers, we first divide the home office/
related organization contract labor costs by total facility medical
care costs to obtain a Home Office/Related Organization Contract Labor
cost weight for the universe of IPF providers. Similar to the other
market basket costs weights, we proposed to trim the Home Office/
Related Organization Contract Labor cost weight to remove outliers.
Since not all hospital-based IPFs will have home office/related
organization contract labor costs (approximately 80 percent of
hospital-based IPFs report having a home office), we proposed to trim
the top one percent of the Home Office/Related Organization Contract
Labor cost weight. Using this proposed methodology, we calculate a Home
Office/Related Organization Contract Labor cost weight for hospital-
based IPFs of 5.1 percent.
Freestanding IPFs are not required to complete Worksheet S-3, part
II. Therefore, to estimate the Home Office/Related Organization
Contract Labor cost weight for freestanding IPFs, we proposed the
following methodology:
Step 1: Using hospital-based IPFs with a home office and also
passing the 1 percent trim as described, we calculate the ratio of the
Home Office/Related Organization Contract Labor cost weight to the
Medicare allowable non-salary, non-capital cost weight (Medicare
allowable non-salary, non-capital costs as a percent of total Medicare
allowable costs).
Step 2: We identify freestanding IPFs that report a home office on
Worksheet S-2, line 140--roughly 87 percent of freestanding IPFs. We
proposed to calculate a Home Office/Related Organization Contract Labor
cost weight for these freestanding IPFs by multiplying the ratio
calculated in Step 1 by the Medicare allowable non-salary, noncapital
cost weight for those freestanding IPFs with a home office.
[[Page 51062]]
Step 3: We then calculate the freestanding IPF cost weight by
multiplying the Home Office/Related Organization Contract Labor cost
weight in Step 2 by the total Medicare allowable costs for freestanding
IPFs with a home office as a percent of total Medicare allowable costs
for all freestanding IPFs (87 percent), which derives a freestanding
Home Office/Related Organization Contract Labor cost weight of 4.2
percent.
To calculate the overall Home Office/Related Organization Contract
Labor cost weight for the 2021-based IPF market basket, we proposed to
weight together the freestanding Home Office/Related Organization
Contract Labor cost weight (4.2 percent) and the hospital-based Home
Office Contract Labor/Related Organization cost weight (5.1 percent)
using total Medicare allowable costs from the sample of hospital-based
IPFs that passed the one percent trim and the universe of freestanding
IPFs. The resulting overall cost weight for Home Office/Related
Organization Contract Labor is 4.7 percent (4.2 percent x 44 percent +
5.1 percent x 56 percent). This is the same methodology used to
calculate the Home Office/Related Organization Contract Labor cost
weight in the 2016-based IPF market basket.
Finally, we proposed to calculate the residual ``All Other'' cost
weight that reflects all remaining costs that are not captured in the
seven cost categories listed. See Table 1 for the resulting cost
weights for these major cost categories that we obtain from the
Medicare cost reports.
[GRAPHIC] [TIFF OMITTED] TR02AU23.001
As we did for the 2016-based IPF market basket, we proposed to
allocate the Contract Labor cost weight to the Wages and Salaries and
Employee Benefits cost weights based on their relative proportions
under the assumption that contract labor costs are comprised of both
wages and salaries, and employee benefits. The Contract Labor
allocation proportion for Wages and Salaries is equal to the Wages and
Salaries cost weight as a percent of the sum of the Wages and Salaries
cost weight and the Employee Benefits cost weight. For the proposed
rule, the rounded percentage is 79 percent; therefore, we proposed to
allocate 79 percent of the Contract Labor cost weight to the Wages and
Salaries cost weight and 21 percent to the Employee Benefits cost
weight. This allocation was 81/19 in the 2016-based IPF market basket
(84 FR 38430). Table 2 shows the Wages and Salaries and Employee
Benefit cost weights after Contract Labor cost weight allocation for
both the 2021-based IPF market basket and 2016-based IPF market basket.
[GRAPHIC] [TIFF OMITTED] TR02AU23.002
We did not receive any comments on our proposed methodology for
developing the major cost weights of the 2021-based IPF market basket.
We are finalizing these major cost weights as proposed.
(3) Derivation of the Detailed Operating Cost Weights
To further divide the ``All Other'' residual cost weight estimated
from the 2021 Medicare cost report data into more detailed cost
categories, we proposed to use the 2012 Benchmark Input-Output (I-O)
``Use Tables/Before Redefinitions/Purchaser Value'' for North American
Industry Classification System (NAICS) 622000, Hospitals, published by
the Bureau of Economic Analysis (BEA). This data is publicly available
at https://www.bea.gov/industry/io_annual.htm. For the 2016-based IPF
market basket, we also used the 2012 Benchmark I-O data, the most
recent data available at the time (84 FR 38431).
The BEA Benchmark I-O data are scheduled for publication every 5
years with the most recent data available for 2012. The 2012 Benchmark
I-O data are derived from the 2012 Economic Census and are the building
blocks for BEA's economic accounts. Thus, they represent the most
comprehensive and complete set of data on the economic processes or
mechanisms by which
[[Page 51063]]
output is produced and distributed.\1\ BEA also produces Annual I-O
estimates; however, while based on a similar methodology, these
estimates reflect less comprehensive and less detailed data sources and
are subject to revision when benchmark data becomes available. Instead
of using the less detailed Annual I-O data, we proposed to inflate the
2012 Benchmark I-O data forward to 2021 by applying the annual price
changes from the respective price proxies to the appropriate market
basket cost categories that are obtained from the 2012 Benchmark I-O
data. We repeat this practice for each year. We then proposed to
calculate the cost shares that each cost category represents of the
inflated 2012 data. These resulting 2021 cost shares are applied to the
``All Other'' residual cost weight to obtain the detailed cost weights
for the 2021-based IPF market basket. For example, the cost for Food:
Direct Purchases represents 5.0 percent of the sum of the ``All Other''
2012 Benchmark I-O Hospital Expenditures inflated to 2021; therefore,
the Food: Direct Purchases cost weight represents 5.0 percent of the
proposed 2021-based IPF market basket's ``All Other'' cost category
(16.7 percent), yielding a ``final'' Food: Direct Purchases cost weight
of 0.8 percent in the 2021-based IPF market basket (0.05 * 16.7 percent
= 0.8 percent).
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\1\ https://www.bea.gov/papers/pdf/IOmanual_092906.pdf.
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Using this methodology, we proposed to derive seventeen detailed
IPF market basket cost category weights from the 2021-based IPF market
basket residual cost weight (16.7 percent). These categories are: (1)
Electricity and Other Non-Fuel Utilities; (2) Fuel: Oil and Gas; (3)
Food: Direct Purchases; (4) Food: Contract Services; (5) Chemicals; (6)
Medical Instruments; (7) Rubber and Plastics; (8) Paper and Printing
Products; (9) Miscellaneous Products; (10) Professional Fees: Labor-
Related; (11) Administrative and Facilities Support Services; (12)
Installation, Maintenance, and Repair Services; (13) All Other Labor-
Related Services; (14) Professional Fees: Nonlabor-Related; (15)
Financial Services; (16) Telephone Services; and (17) All Other
Nonlabor-Related Services.
We did not receive any comments on our methodology to use the BEA
I-O data to derive the detailed operating cost weights. We are
finalizing this methodology as we proposed. We note that we did receive
one comment on the derivation of the Professional Fees: Labor-Related
cost weight, which we discuss in section IV.A.5 of this final rule.
(4) Derivation of the Detailed Capital Cost Weights
As described in section IV.A.3.a.(2) of this final rule, we
proposed a Capital-Related cost weight of 7.2 percent as obtained from
the 2021 Medicare cost reports for freestanding and hospital-based IPF
providers. We proposed to then separate this total Capital-Related cost
weight into more detailed cost categories.
Using 2021 Medicare cost reports, we are able to group Capital-
Related costs into the following categories: Depreciation, Interest,
Lease, and Other Capital-Related costs. For each of these categories,
we proposed to determine separately for hospital-based IPFs and
freestanding IPFs what proportion of total capital-related costs the
category represents.
For freestanding IPFs, using Medicare Cost Report data on Worksheet
A-7 part III, we proposed to derive the proportions for Depreciation
(column 9), Interest (column 11), Lease (column 10), and Other Capital-
related costs (column 12 through 14), which is similar to the
methodology used for the 2016-based IPF market basket.
For hospital-based IPFs, data for these four categories are not
reported separately for the hospital-based IPF; therefore, we proposed
to derive these proportions using data reported on Worksheet A-7 for
the total facility. We are assuming the cost shares for the overall
hospital are representative for the hospital-based IPF unit. For
example, if depreciation costs make up 60 percent of total capital
costs for the entire facility, we believe it is reasonable to assume
that the hospital-based IPF would also have a 60 percent proportion
because it is a unit contained within the total facility. This is the
same methodology used for the 2016-based IPF market basket (84 FR
38431).
To combine each detailed capital cost weight for freestanding and
hospital-based IPFs into a single capital cost weight for the 2021-
based IPF market basket, we proposed to weight together the shares for
each of the categories (Depreciation, Interest, Lease, and Other
Capital-Related costs) based on the share of total capital costs each
provider type represents of the total capital costs for all IPFs for
2021. Applying this methodology results in proportions of total
capital-related costs for Depreciation, Interest, Lease and Other
Capital-Related costs that are representative of the universe of IPF
providers. This is the same methodology used for the 2016-based IPF
market basket (84 FR 38432).
Lease costs are unique in that they are not broken out as a
separate cost category in the 2021-based IPF market basket. Rather, we
proposed to proportionally distribute these costs among the cost
categories of Depreciation, Interest, and Other Capital-Related costs,
reflecting the assumption that the underlying cost structure of leases
is similar to that of Capital-Related costs in general. As was done for
the 2016-based IPF market basket, we proposed to assume that 10 percent
of the lease costs as a proportion of total Capital-Related costs
represent overhead and assign those costs to the Other Capital-Related
cost category accordingly. We proposed to distribute the remaining
lease costs proportionally across the three cost categories
(Depreciation, Interest, and Other Capital-Related) based on the
proportion that these categories comprise of the sum of the
Depreciation, Interest, and Other Capital-Related cost categories
(excluding lease expenses). This would result in three primary Capital-
Related cost categories in the 2021-based IPF market basket:
Depreciation, Interest, and Other Capital-Related costs. This is the
same methodology used for the 2016-based IPF market basket (84 FR
38432). The allocation of these lease expenses is shown in Table 3.
Finally, we proposed to further divide the Depreciation and
Interest cost categories. We proposed to separate Depreciation into the
following two categories: (1) Building and Fixed Equipment; and (2)
Movable Equipment. We proposed to separate Interest into the following
two categories: (1) Government/Nonprofit; and (2) For-profit.
To disaggregate the Depreciation cost weight, we need to determine
the percent of total Depreciation costs for IPFs that is attributable
to Building and Fixed Equipment, which we hereafter refer to as the
``fixed percentage.'' For the 2021-based IPF market basket, we proposed
to use slightly different methods to obtain the fixed percentages for
hospital-based IPFs compared to freestanding IPFs.
For freestanding IPFs, we proposed to use depreciation data from
Worksheet A-7 of the 2021 Medicare cost reports. However, for hospital-
based IPFs, we determined that the fixed percentage for the entire
facility may not be representative of the hospital-based IPF unit due
to the entire facility likely employing more sophisticated movable
assets that are not utilized by the hospital-based IPF. Therefore, for
hospital-based IPFs, we proposed to
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calculate a fixed percentage using: (1) building and fixture capital
costs allocated to the hospital-based IPF unit as reported on Worksheet
B, part I, column 1, line 40; and (2) building and fixture capital
costs for the top five ancillary cost centers utilized by hospital-
based IPFs accounting for 82 percent of hospital-based IPF ancillary
total costs: Clinic (Worksheet B, part I, column 1, line 90), Drugs
Charged to Patients (Worksheet B, part I, column 1, line 73), Emergency
(Worksheet B, part I, column 1, line 91), Laboratory (Worksheet B, part
I, column 1, line 60) and Radiology--Diagnostic (Worksheet B, part I,
column 1, line 54). We proposed to weight these two fixed percentages
(inpatient and ancillary) using the proportion that each capital cost
type represents of total capital costs in the 2021-based IPF market
basket. We proposed to then weight the fixed percentages for hospital-
based and freestanding IPFs together using the proportion of total
capital costs each provider type represents. For both freestanding and
hospital-based IPFs, this is the same methodology used for the 2016-
based IPF market basket (84 FR 38432).
To disaggregate the Interest cost weight, we determined the percent
of total interest costs for IPFs that are attributable to government
and nonprofit facilities, which is hereafter referred to as the
``nonprofit percentage,'' as price pressures associated with these
types of interest costs tend to differ from those for for-profit
facilities. For the 2021-based IPF market basket, we proposed to use
interest costs data from Worksheet A-7 of the 2021 Medicare cost
reports for both freestanding and hospital-based IPFs. We proposed to
determine the percent of total interest costs that are attributed to
government and nonprofit IPFs separately for hospital-based and
freestanding IPFs. We then proposed to weight the nonprofit percentages
for hospital-based and freestanding IPFs together using the proportion
of total capital costs that each provider type represents.
Table 3 provides the proposed detailed capital cost share
composition estimated from the 2021 IPF Medicare cost reports. These
detailed capital cost share composition percentages are applied to the
total Capital-Related cost weight of 7.2 percent explained in detail in
sections IV.A.3.a.(1)(h) and IV.A.3.a.(2) of this final rule.
BILLING CODE 4120-010-P
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We did not receive any comments on our proposed methodology for
developing the detailed capital cost weights of the 2021-based IPF
market basket. We are finalizing these detailed capital cost weights as
proposed.
(5) 2021-Based IPF Market Basket Cost Categories and Weights
Table 4 compares the cost categories and weights for the finalized
2021-based IPF market basket compared to the 2016-based IPF market
basket.
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b. Selection of Price Proxies
After developing the cost weights for the 2021-based IPF market
basket, we proposed to select the most appropriate wage and price
proxies currently available to represent the rate of price change for
each expenditure category. For the majority of the cost weights, we
base the price proxies on Bureau of Labor Statistics (BLS) data and
grouped them into one of the following BLS categories:
Employment Cost Indexes (ECIs): measure the rate of change
in employment wage rates and employer costs for employee benefits per
hour worked. These indexes are fixed-weight indexes and strictly
measure the change in wage rates and employee benefits per hour. ECIs
are superior to Average Hourly Earnings (AHE) as price proxies for
input price indexes because they are not affected by shifts in
occupation or industry mix, and because they measure pure price change
and are available by both occupational group and by industry. The
industry ECIs are based on the NAICS and the occupational ECIs are
based on the Standard Occupational Classification System (SOC).
Producer Price Indexes (PPI): measure the average change
over time in
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the selling prices received by domestic producers for their output. The
prices included in the PPI are from the first commercial transaction
for many products and some services (https://www.bls.gov/ppi/).
Consumer Price Indexes (CPIs): measure the average change
over time in the prices paid by urban consumers for a market basket of
consumer goods and services (https://www.bls.gov/cpi/). CPIs are only
used when the purchases are similar to those of retail consumers rather
than purchases at the wholesale level, or if no appropriate PPIs are
available.
We evaluated the price proxies using the criteria of reliability,
timeliness, availability, and relevance:
Reliability: indicates that the index is based on valid
statistical methods and has low sampling variability. Widely accepted
statistical methods ensure that the data were collected and aggregated
in a way that can be replicated. Low sampling variability is desirable
because it indicates that the sample reflects the typical members of
the population. (Sampling variability is variation that occurs by
chance because only a sample was surveyed rather than the entire
population.)
Timeliness: implies that the proxy is published regularly,
preferably at least once a quarter. The market baskets are updated
quarterly and, therefore, it is important for the underlying price
proxies to be up-to-date, reflecting the most recent data available. We
believe that using proxies that are published regularly (at least
quarterly, whenever possible) helps to ensure that we are using the
most recent data available to update the market basket. We strive to
use publications that are disseminated frequently, because we believe
that this is an optimal way to stay abreast of the most current data
available.
Availability: means that the proxy is publicly available.
We prefer that our proxies are publicly available because this will
help ensure that our market basket updates are as transparent to the
public as possible. In addition, this enables the public to be able to
obtain the price proxy data on a regular basis.
Relevance: means that the proxy is applicable and
representative of the cost category weight to which it is applied. The
CPIs, PPIs, and ECIs that we proposed in this regulation meet these
criteria. Therefore, we believe that they continue to be the best
measure of price changes for the cost categories to which they would be
applied.
Table 13 lists all price proxies that we proposed to use for the
2021-based IPF market basket. A detailed explanation of the price
proxies we proposed for each cost category weight is provided below.
(1) Price Proxies for the Operating Portion of the 2021-Based IPF
Market Basket
(a) Wages and Salaries
There is not a published wage proxy that we believe represents the
occupational distribution of workers in IPFs. To measure wage price
growth in the 2021-based IPF market basket, we proposed to apply a
proxy blend based on six occupational subcategories within the Wages
and Salaries category, which would reflect the IPF occupational mix, as
was done for the 2016-based IPF market basket.
We proposed to use the National Industry-Specific Occupational
Employment and Wage estimates for NAICS 622200, Psychiatric & Substance
Abuse Hospitals, published by the BLS Occupational Employment and Wage
Statistics (OEWS) program, as the data source for the wage cost shares
in the wage proxy blend. We note that in the spring of 2021, the
Occupational Employment Statistics (OES) program began using the name
Occupational Employment and Wage Statistics (OEWS) to better reflect
the range of data available from the program. Data released on or after
March 31, 2021 reflect the new program name. We proposed to use May
2021 OEWS data. Detailed information on the methodology for the
national industry-specific occupational employment and wage estimates
survey can be found at https://www.bls.gov/oes/current/oes_tec.htm. For
the 2016-based IPF market basket, we used May 2016 OES data.
Based on the OEWS data, there are six wage subcategories:
Management; NonHealth Professional and Technical; Health Professional
and Technical; Health Service; NonHealth Service; and Clerical. Table 5
lists the 2021 occupational assignments for the six wage subcategories;
these are the same occupational groups used in the 2016-based IPF
market basket.
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Total expenditures by occupation (that is, occupational assignment)
were calculated by taking the OEWS number of employees multiplied by
the OEWS annual average salary. These expenditures were aggregated
based on the six groups in Table 5. We next calculated the proportion
of each group's expenditures relative to the total expenditures of all
six groups. These proportions, listed in Table 6, represent the weights
used in the wage proxy blend. We then proposed to use the published
wage proxies in Table 6 for each of the six groups (that is, wage
subcategories) as we believe these six price proxies are the most
technically appropriate indices available to measure the price growth
of the Wages and Salaries cost category. These are the same price
proxies used in the 2016-based IPF market basket (84 FR 38437).
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A comparison of the yearly changes from FY 2021 to FY 2024 for the
2021-based IPF wage blend and the 2016-based IPF wage blend is shown in
Table 7. The average annual growth rate is the same for both price
proxies over 2021-2024.
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(b) Employee Benefits
To measure benefits price growth in the 2021-based IPF market
basket, we proposed to apply a benefits proxy blend based on the same
six subcategories and the same six blend weights for the wage proxy
blend. These subcategories and blend weights are listed in Table 8.
The benefit ECIs, listed in Table 8, are not publicly available.
Therefore, an ``ECIs for Total Benefits'' is calculated using publicly
available ``ECIs for Total Compensation'' for each subcategory and the
relative importance of wages within that subcategory's total
compensation. This is the same benefits ECI methodology that we
implemented in our 2016-based IPF market basket as well as used in the
IPPS, SNF, Home Health Agency (HHA), IRF, LTCH, and End-Stage Renal
Disease (ESRD) market baskets. We believe that the six price proxies
listed in Table 8 are the most technically appropriate indices to
measure the price growth of the Employee Benefits cost category in the
2021-based IPF market basket.
[[Page 51070]]
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A comparison of the yearly changes from FY 2021 to FY 2024 for the
2021-based IPF benefit proxy blend and the 2016-based IPF benefit proxy
is shown in Table 9. The average annual growth rate is the same for
both price proxies over 2021 through 2024.
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(c) Electricity and Other Non-Fuel Utilities
We proposed to use the PPI Commodity Index for Commercial Electric
Power (BLS series code WPU0542) to measure the price growth of this
cost category (which we proposed to rename from Electricity to
Electricity and Other Non-Fuel Utilities). This is the same price proxy
used in the 2016-based IPF market basket (84 FR 38438).
(d) Fuel: Oil and Gas
Similar to the 2016-based IPF market basket, for the 2021-based IPF
market basket, we proposed to use a blend of the PPI for Petroleum
Refineries and the PPI Commodity for Natural Gas. Our analysis of the
Bureau of Economic Analysis' 2012 Benchmark Input-Output data (use
table before redefinitions, purchaser's value for NAICS 622000
[Hospitals]), shows that Petroleum Refineries expenses account for
approximately 90 percent and Natural Gas expenses account for
approximately 10 percent of Hospitals' (NAICS 622000) total Fuel: Oil
and Gas expenses. Therefore, we proposed to use a blend of 90 percent
of the PPI for Petroleum Refineries (BLS series code PCU324110324110)
and 10 percent of the PPI Commodity Index for Natural Gas (BLS series
code WPU0531) as the price proxy for this cost category. This is the
same blend that was used for the 2016-based IPF market basket (84 FR
38438).
(e) Professional Liability Insurance
We proposed to use the CMS Hospital Professional Liability Index to
measure changes in PLI premiums. To generate this index, we collect
commercial insurance premiums for a fixed level of coverage while
holding non-price factors constant (such as a change in the level of
coverage). This is the same proxy used in the 2016-based IPF market
basket (84 FR 38438).
(f) Pharmaceuticals
We proposed to use the PPI for Pharmaceuticals for Human Use,
Prescription (BLS series code WPUSI07003) to measure the price growth
of this cost category. This is the same proxy used in the 2016-based
IPF market basket (84 FR 38438).
[[Page 51071]]
(g) Food: Direct Purchases
We proposed to use the PPI for Processed Foods and Feeds (BLS
series code WPU02) to measure the price growth of this cost category.
This is the same proxy used in the 2016-based IPF market basket (84 FR
38438).
(h) Food: Contract Purchases
We proposed to use the CPI for Food Away From Home (BLS series code
CUUR0000SEFV) to measure the price growth of this cost category. This
is the same proxy used in the 2016-based IPF market basket (84 FR
38438).
(i) Chemicals
Similar to the 2016-based IPF market basket, we proposed to use a
four-part blended PPI as the proxy for the chemical cost category in
the 2021-based IPF market basket. The proposed blend is composed of the
PPI for Industrial Gas Manufacturing, Primary Products (BLS series code
PCU325120325120P), the PPI for Other Basic Inorganic Chemical
Manufacturing (BLS series code PCU32518-32518-), the PPI for Other
Basic Organic Chemical Manufacturing (BLS series code PCU32519-32519-),
and the PPI for Other Miscellaneous Chemical Product Manufacturing (BLS
series code PCU325998325998). For the 2021-based IPF market basket, we
proposed to derive the weights for the PPIs using the 2012 Benchmark I-
O data.
Table 10 shows the weights for each of the four PPIs used to create
the blended Chemical proxy for the 2021-based IPF market basket. This
is the same blend that was used for the 2016-based IPF market basket
(84 FR 38439).
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(j) Medical Instruments
We proposed to use a blended price proxy for the Medical
Instruments category, as shown in Table 11. The 2012 Benchmark I-O data
shows the majority of medical instruments and supply costs are for
NAICS 339112--Surgical and medical instrument manufacturing costs
(approximately 56 percent) and NAICS 339113--Surgical appliance and
supplies manufacturing costs (approximately 43 percent). Therefore, we
proposed to use a blend of these two price proxies. To proxy the price
changes associated with NAICS 339112, we proposed to use the PPI for
Surgical and medical instruments (BLS series code WPU1562). This is the
same price proxy we used in the 2016-based IPF market basket. To proxy
the price changes associated with NAICS 339113, we proposed to use a
50/50 blend of the PPI for Medical and surgical appliances and supplies
(BLS series code WPU1563) and the PPI for Miscellaneous products,
Personal safety equipment and clothing (BLS series code WPU1571). We
proposed to include the latter price proxy as it will reflect personal
protective equipment including but not limited to face shields and
protective clothing. The 2012 Benchmark I-O data does not provide
specific expenses for these products; however, we recognize that this
category reflects costs faced by IPFs.
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(k) Rubber and Plastics
We proposed to use the PPI for Rubber and Plastic Products (BLS
series code WPU07) to measure price growth of this cost category. This
is the same proxy used in the 2016-based IPF market basket (84 FR
38439).
(l) Paper and Printing Products
We proposed to use the PPI for Converted Paper and Paperboard
Products (BLS series code WPU0915) to measure the price growth of this
cost category. This is the same proxy used in the 2016-based IPF market
basket (84 FR 38439).
(m) Miscellaneous Products
We proposed to use the PPI for Finished Goods Less Food and Energy
(BLS series code WPUFD4131) to measure the price growth of this cost
category. This is the same proxy used in the 2016-based IPF market
basket (84 FR 38439).
(n) Professional Fees: Labor-Related
We proposed to use the ECI for Total Compensation for Private
Industry workers in Professional and Related (BLS series code
CIU2010000120000I) to measure the price growth of this category. This
is the same proxy used in the 2016-based IPF market basket (84 FR
38439).
[[Page 51072]]
(o) Administrative and Facilities Support Services
We proposed to use the ECI for Total Compensation for Private
Industry workers in Office and Administrative Support (BLS series code
CIU2010000220000I) to measure the price growth of this category. This
is the same proxy used in the 2016-based IPF market basket (84 FR
38439).
(p) Installation, Maintenance, and Repair Services
We proposed to use the ECI for Total Compensation for Civilian
workers in Installation, Maintenance, and Repair (BLS series code
CIU1010000430000I) to measure the price growth of this cost category.
This is the same proxy used in the 2016-based IPF market basket (84 FR
38439).
(q) All Other: Labor-Related Services
We proposed to use the ECI for Total Compensation for Private
Industry workers in Service Occupations (BLS series code
CIU2010000300000I) to measure the price growth of this cost category.
This is the same proxy used in the 2016-based IPF market basket (84 FR
38439).
(r) Professional Fees: Nonlabor-Related
We proposed to use the ECI for Total Compensation for Private
Industry workers in Professional and Related (BLS series code
CIU2010000120000I) to measure the price growth of this category. This
is the same proxy used in the 2016-based IPF market basket (84 FR
38439).
(s) Financial Services
We proposed to use the ECI for Total Compensation for Private
Industry workers in Financial Activities (BLS series code
CIU201520A000000I) to measure the price growth of this cost category.
This is the same proxy used in the 2016-based IPF market basket (84 FR
38439).
(t) Telephone Services
We proposed to use the CPI for Telephone Services (BLS series code
CUUR0000SEED) to measure the price growth of this cost category. This
is the same proxy used in the 2016-based IPF market basket (84 FR
38439).
(u) All Other: Nonlabor-Related Services
We proposed to use the CPI for All Items Less Food and Energy (BLS
series code CUUR0000SA0L1E) to measure the price growth of this cost
category. This is the same proxy used in the 2016-based IPF market
basket (84 FR 38439).
We did not receive any comments on our proposed price proxies for
the operating portion of the 2021-based IPF market basket. We are
finalizing these price proxies as proposed.
Table 13 lists all price proxies that we are finalizing for the
2021-based IPF market basket.
(2) Price Proxies for the Capital Portion of the 2021-Based IPF Market
Basket
(a) Capital Price Proxies Prior to Vintage Weighting
We proposed to use the same price proxies for the capital-related
cost categories in the 2021-based IPF market basket as were used in the
2016-based IPF market basket, which are provided in Table 13 and
described below. Specifically, we proposed to proxy:
Depreciation: Building and Fixed Equipment cost category
by BEA's Chained Price Index for Nonresidential Construction for
Hospitals and Special Care Facilities (BEA Table 5.4.4. Price Indexes
for Private Fixed Investment in Structures by Type).
Depreciation: Movable Equipment cost category by the PPI
for Machinery and Equipment (BLS series code WPU11).
Nonprofit Interest cost category by the average yield on
domestic municipal bonds (Bond Buyer 20-bond index).
For-profit Interest cost category by the iBoxx AAA
Corporate Bond Yield index
Other Capital-Related cost category by the CPI-U for Rent
of Primary Residence (BLS series code CUUS0000SEHA).
We believe these are the most appropriate proxies for IPF capital-
related costs that meet our selection criteria of relevance,
timeliness, availability, and reliability. We also proposed to vintage
weight the capital price proxies for Depreciation and Interest to
capture the long-term consumption of capital. This vintage weighting
method is similar to the method used for the 2016-based IPF market
basket (84 FR 38440) and is described below.
(b) Vintage Weights for Price Proxies
Because capital is acquired and paid for over time, capital-related
expenses in any given year are determined by both past and present
purchases of physical and financial capital. The vintage-weighted
capital-related portion of the 2021-based IPF market basket is intended
to capture the long-term consumption of capital, using vintage weights
for depreciation (physical capital) and interest (financial capital).
These vintage weights reflect the proportion of capital-related
purchases attributable to each year of the expected life of building
and fixed equipment, movable equipment, and interest. We proposed to
use vintage weights to compute vintage-weighted price changes
associated with depreciation and interest expenses.
Capital-related costs are inherently complicated and are determined
by complex capital-related purchasing decisions, over time, based on
such factors as interest rates and debt financing. In addition, capital
is depreciated over time instead of being consumed in the same period
it is purchased. By accounting for the vintage nature of capital, we
are able to provide an accurate and stable annual measure of price
changes. Annual non-vintage price changes for capital are unstable due
to the volatility of interest rate changes, and therefore, do not
reflect the actual annual price changes for IPF capital-related costs.
The capital-related component of the 2021-based IPF market basket
reflects the underlying stability of the capital-related acquisition
process.
The methodology used to calculate the vintage weights for the 2021-
based IPF market basket is the same as that used for the 2016-based IPF
market basket (84 FR 38439 through 38441) with the only difference
being the inclusion of more recent data. To calculate the vintage
weights for depreciation and interest expenses, we first need a time
series of capital-related purchases for building and fixed equipment
and movable equipment. We found no single source that provides an
appropriate time series of capital-related purchases by hospitals for
all of the above components of capital purchases. The early Medicare
cost reports did not have sufficient capital-related data to meet this
need. Data we obtained from the American Hospital Association (AHA) do
not include annual capital-related purchases. However, we are able to
obtain data on total expenses back to 1963 from the AHA. Consequently,
we proposed to use data from the AHA Panel Survey and the AHA Annual
Survey to obtain a time series of total expenses for hospitals. We then
proposed to use data from the AHA Panel Survey supplemented with the
ratio of depreciation to total hospital expenses obtained from the
Medicare cost reports to derive a trend of annual depreciation expenses
for 1963 through 2020, which is the latest year of AHA data available.
We proposed to separate these depreciation expenses into annual amounts
of building and fixed equipment depreciation and movable equipment
depreciation as determined earlier. From these annual depreciation
amounts, we derive annual end-of-year
[[Page 51073]]
book values for building and fixed equipment and movable equipment
using the expected life for each type of asset category. While data is
not available that is specific to IPFs, we believe this information for
all hospitals serves as a reasonable alternative for the pattern of
depreciation for IPFs.
To continue to calculate the vintage weights for depreciation and
interest expenses, we also need to account for the expected lives for
Building and Fixed Equipment, Movable Equipment, and Interest for the
2021-based IPF market basket. We proposed to calculate the expected
lives using Medicare cost report data from freestanding and hospital-
based IPFs. The expected life of any asset can be determined by
dividing the value of the asset (excluding fully depreciated assets) by
its current year depreciation amount. This calculation yields the
estimated expected life of an asset if the rates of depreciation were
to continue at current year levels, assuming straight-line
depreciation. We proposed to determine the expected life of building
and fixed equipment separately for hospital-based IPFs and freestanding
IPFs, and then weight these expected lives using the percent of total
capital costs each provider type represents. We proposed to apply a
similar method for movable equipment. Using these proposed methods, we
determined the average expected life of building and fixed equipment to
be equal to 25 years, and the average expected life of movable
equipment to be equal to 12 years. For the expected life of interest,
we believe vintage weights for interest should represent the average
expected life of building and fixed equipment because, based on
previous research described in the FY 1997 IPPS final rule (61 FR
46198), the expected life of hospital debt instruments and the expected
life of buildings and fixed equipment are similar. We note that for the
2016-based IPF market basket, the expected life of building and fixed
equipment is 22 years, and the expected life of movable equipment is 11
years (84 FR 38441).
Multiplying these expected lives by the annual depreciation amounts
results in annual year-end asset costs for building and fixed equipment
and movable equipment. We then calculate a time series, beginning in
1964, of annual capital purchases by subtracting the previous year's
asset costs from the current year's asset costs.
For the building and fixed equipment and movable equipment vintage
weights, we proposed to use the real annual capital-related purchase
amounts for each asset type to capture the actual amount of the
physical acquisition, net of the effect of price inflation. These real
annual capital-related purchase amounts are produced by deflating the
nominal annual purchase amount by the associated price proxy as
provided earlier in this final rule. For the interest vintage weights,
we proposed to use the total nominal annual capital-related purchase
amounts to capture the value of the debt instrument (including, but not
limited to, mortgages and bonds). Using these capital-related purchase
time series specific to each asset type, we proposed to calculate the
vintage weights for building and fixed equipment, for movable
equipment, and for interest.
The vintage weights for each asset type are deemed to represent the
average purchase pattern of the asset over its expected life (in the
case of building and fixed equipment and interest, 25 years, and in the
case of movable equipment, 12 years). For each asset type, we used the
time series of annual capital-related purchase amounts available from
2020 back to 1964. These data allow us to derive thirty-three 25-year
periods of capital-related purchases for building and fixed equipment
and interest, and forty-six 12-year periods of capital-related
purchases for movable equipment. For each 25-year period for building
and fixed equipment and interest, or 12-year period for movable
equipment, we calculate annual vintage weights by dividing the capital-
related purchase amount in any given year by the total amount of
purchases over the entire 25-year or 12-year period. This calculation
is done for each year in the 25-year or 12-year period and for each of
the periods for which we have data. We then calculate the average
vintage weight for a given year of the expected life by taking the
average of these vintage weights across the multiple periods of data.
The vintage weights for the capital-related portion of the 2021-based
IPF market basket and the 2016-based IPF market basket are presented in
Table 12.
[[Page 51074]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.013
The process of creating vintage-weighted price proxies requires
applying the vintage weights to the price proxy index where the last
applied vintage weight in Table 12 is applied to the most recent data
point. We have provided on the CMS website an example of how the
vintage weighting price proxies are calculated, using example vintage
weights and example price indices. The example can be found at https://www.cms.gov/Research-Statistics-Data-and-Systems/Statistics-Trends-and-Reports/MedicareProgramRatesStats/MarketBasketResearch.html in the zip
file titled ``Weight Calculations as described in the IPPS FY 2010
Proposed Rule.''
We did not receive any comments on our proposed price proxies for
the capital portion of the 2021-based IPF market basket. We are
finalizing these price proxies as proposed.
(3) Summary of Price Proxies of the 2021-Based IPF Market Basket
Table 13 shows both the operating and capital price proxies that we
are finalizing for the 2021-based IPF market basket.
[[Page 51075]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.014
[[Page 51076]]
After consideration of public comments, we are finalizing the 2021-
based IPF market basket as proposed.
4. FY 2024 Market Basket Update and Productivity Adjustment
a. FY 2024 Market Basket Update
For FY 2024 (that is, beginning October 1, 2023 and ending
September 30, 2024), we proposed to use an estimate of the proposed
2021-based IPF market basket increase factor to update the IPF PPS base
payment rate. Consistent with historical practice, we estimate the
market basket update for the IPF PPS based on IHS Global Inc.'s (IGI)
forecast. IGI is a nationally recognized economic and financial
forecasting firm with which CMS contracts to forecast the components of
the market baskets.
Using IGI's fourth quarter 2022 forecast with historical data
through the third quarter of 2022, the projected proposed 2021-based
IPF market basket increase factor for FY 2024 was 3.2 percent. We also
proposed that if more recent data were subsequently available (for
example, a more recent estimate of the market basket increase factor)
we would use such data, to determine the FY 2024 update in the final
rule.
Based on IGI's second quarter 2023 forecast with historical data
through the first quarter of 2023, the 2021-based IPF market basket
increase percentage for FY 2024 is 3.5 percent. For comparison, the
current 2016-based IPF market basket is also projected to increase by
3.5 percent in FY 2024 based on IGI's second quarter 2023 forecast.
Table 14 compares the 2021-based IPF market basket and the 2016-based
IPF market basket percent changes. On average, the two indexes produce
similar updates to one another, with the 4-year average historical
growth rates (for FY 2019-FY 2022) of the 2021-based IPF market basket
being equal to 3.2 percent compared to the 2016-based IPF market basket
with 3.2 percent.
[GRAPHIC] [TIFF OMITTED] TR02AU23.015
BILLING CODE 4120-010-C
b. Productivity Adjustment
Section 1886(s)(2)(A)(i) of the Act requires the application of the
productivity adjustment described in section 1886(b)(3)(B)(xi)(II) of
the Act to the IPF PPS for the RY beginning in 2012 (that is, a RY that
coincides with a FY) and each subsequent RY. The statute defines the
productivity adjustment to be equal to the 10-year moving average of
changes in annual economy-wide, private nonfarm business multifactor
productivity (as projected by the Secretary for the 10-year period
ending with the applicable FY, year, cost reporting period, or other
annual period) (the ``productivity adjustment''). The United States
Department of Labor's Bureau of Labor Statistics (BLS) publishes the
official measures of productivity for the United States economy. We
note that previously the productivity measure referenced in section
1886(b)(3)(B)(xi)(II) of the Act, was published by BLS as private
nonfarm business multifactor productivity. Beginning with the November
18, 2021 release of productivity data, BLS replaced the term
multifactor productivity (MFP) with total factor productivity (TFP).
BLS noted that this is a change in terminology only and will not affect
the data or methodology. As a result of the BLS name change, the
productivity measure referenced in section 1886(b)(3)(B)(xi)(II) of the
Act is now published by BLS as private nonfarm business total factor
productivity. However, as mentioned above, the data and methods are
unchanged. We refer readers to www.bls.gov for the BLS historical
published TFP data. A complete description of IGI's TFP projection
methodology is available on the CMS website at https://www.cms.gov/
research-statistics-data-and-systems/statistics-trends-and-reports/
[[Page 51077]]
medicareprogramratesstats/marketbasketresearch. In addition, in the FY
2022 IPF PPS final rule (86 FR 42611), we noted that effective with FY
2022 and forward, CMS changed the name of this adjustment to refer to
it as the productivity adjustment rather than the MFP adjustment.
Using IGI's fourth quarter 2022 forecast, the 10-year moving
average growth of TFP for FY 2024 was projected to be 0.2 percent.
Thus, in accordance with section 1886(s)(2)(A)(i) of the Act, we
proposed to calculate the FY 2024 market basket update, which is used
to determine the applicable percentage increase for the IPF payments,
using IGI's fourth quarter 2022 forecast of the proposed 2021-based IPF
market basket. We proposed to then reduce this percentage increase by
the estimated productivity adjustment for FY 2024 of 0.2 percentage
point (the 10-year moving average growth of TFP for the period ending
FY 2024 based on IGI's fourth quarter 2022 forecast). Therefore, the
proposed FY 2024 IPF update was equal to 3.0 percent (3.2 percent
market basket update reduced by the 0.2 percentage point productivity
adjustment). Furthermore, we proposed that if more recent data became
available after the publication of the proposed rule and before the
publication of the final rule (for example, a more recent estimate of
the productivity adjustment), we would use such data, if appropriate,
to determine the FY 2024 productivity adjustment in the final rule.
Using IGI's second quarter 2023 forecast, the 10-year moving
average growth of TFP for FY 2024 is projected to be 0.2 percent. Thus,
in accordance with section 1886(s)(2)(A)(i) of the Act, we calculate
the FY 2024 market basket update, which is used to determine the
applicable percentage increase for the IPF payments, using IGI's second
quarter 2023 forecast of the 2021-based IPF market basket. We then
reduce this percentage increase by the estimated productivity
adjustment for FY 2024 of 0.2 percentage point (the 10-year moving
average growth of TFP for the period ending FY 2024 based on IGI's
second quarter 2023 forecast). Therefore, the FY 2024 IPF update is
equal to 3.3 percent (3.5 percent market basket update reduced by the
0.2 percentage point productivity adjustment).
We invited public comment on our proposals for the FY 2024 market
basket update and productivity adjustment. The following is a summary
of the public comments received on the proposed FY 2024 market basket
update and productivity adjustment.
Comment: Several commenters expressed concern about the proposed
2021-based IPF market basket increase factor for FY 2024 of 3.2
percent. They stated that hospitals throughout the country face
enormous cost pressures, with labor costs (due to increased demand and
workforce shortages) leading to this dramatic increase in overall cost
pressure. They also noted the significant cost increases for drugs,
medical supplies, and personal protective equipment since before the
PHE. The commenters stated that the cumulative effect of this
inflationary pressure coupled with the proposed low Medicare payment
increases for FY 2024 will continue to have negative effects on IPF
operating margins. They cited that the Medicare Payment Advisory
Commission determined that Medicare has failed to cover the cost of
caring for patients in hospital-based and freestanding nonprofit IPFs
since at least 2016.
The commenters also noted that CMS proposed that if more recent
data became available after the publication of the proposed rule and
before the publication of the final rule that CMS would use such data
to determine the FY 2024 update in the final rule. They recommended CMS
use more recent data and implement a payment rate for FY 2024 that more
accurately reflects current costs, rather than relying on data that
preceded the extraordinary inflation they are experiencing. Some
commenters suggested CMS use other methods to determine the market
basket update, such as the average growth rate in allowable Medicare
costs per risk-adjusted discharge for IPFs between FY 2019 and FY 2021
to calculate the FY 2024 final rule market basket update. They stated
that if CMS fails to provide an adequate market basket update, they are
deeply concerned inadequate payments will result in reduced access to
inpatient psychiatric services for Medicare beneficiaries.
Response: We appreciate the commenters' concerns regarding
inflationary pressure facing IPFs and the proposed FY 2024 market
basket update. As stated in Section IV.A.2 in this final rule, the IPF
market basket (including the proposed 2021-based and other CMS market
baskets) is a fixed-weight, Laspeyres-type index that measures price
changes over time. Since the inception of the IPF PPS, the IPF payment
rates (with the exception of statutorily mandated updates) have been
updated by a projection of a market basket percentage increase, which
is designed to measure price inflation for IPF providers and does not
reflect increases in costs associated with changes in the volume or
intensity of input goods and services (such as the quantity of labor
used). In this way, the IPF market basket is consistent in concept and
methodology with market baskets used for other CMS PPS updates,
including IPPS, SNF, and HHA. The longstanding IPF market basket
methodology establishes a market basket that appropriately reflects
expectations, based on the latest available data, of price inflation
for IPF providers for FY 2024. It would be inappropriate for the IPF
market basket to reflect the method proposed by the commenter where the
update would be based on increases in Medicare allowable costs per
risk-adjusted discharge from a past period, since that measure would
incorporate changes in costs that are not solely reflective of price
inflation that is intended to be captured by the market basket update
in the IPF PPS.
The projection of the 2021-based IPF market basket is based on the
most recent forecast from IHS Global Inc.--a nationally recognized
economic and financial forecasting firm with which CMS contracts to
forecast the price proxies of the market baskets. For this final rule,
based on the more recent IGI second quarter 2023 forecast with
historical data through the first quarter of 2023, the projected 2021-
based IPF market basket increase factor for FY 2024 is 3.5 percent,
which is 0.3 percentage point higher than the projected FY 2024 market
basket increase factor in the proposed rule, and reflects an increase
in compensation prices of 4.0 percent. We note that the 10-year
historical average (2013-2022) growth rate of the 2021-based IPF market
basket is 2.4 percent with an average growth rate in compensation
prices of 2.5 percent.
Therefore, consistent with our historical practice of estimating
market basket increases based on the best available data, we are
finalizing a market basket increase percentage of 3.5 percent for FY
2024.
Comment: Several commenters expressed concern about the application
of the productivity adjustment, stating that the PHE has had
unimaginable impacts on hospital productivity. They state that even
before the PHE, OACT indicated that hospital productivity will be less
than the general economy-wide productivity, which is the measure that
is required by law to be used to derive the productivity adjustment.
Given that CMS is required by statute to implement a productivity
adjustment to the market basket update, commenters asked the agency to
work with the Congress to permanently eliminate this unjustified
[[Page 51078]]
reduction to hospital payments. Further, they asked CMS to use its
authority under section 1886(s) of the Act to remove the productivity
adjustment for any fiscal year that was covered under PHE determination
(that is, 2020 (0.4 percent), 2021 (0.0 percent), 2022 (0.7 percent),
and 2023 (0.3 percent)) from the calculation of the market basket
update for FY 2024 and any year thereafter.
Response: Section 1886(s)(2)(A)(i) of the Act requires the
application of the productivity adjustment described in section
1886(b)(3)(xi)(II) of the Act. As required by statute, the FY 2024
productivity adjustment is derived based on the 10-year moving average
growth in economy-wide productivity for the period ending FY 2024. We
recognize the concerns of the commenters regarding the appropriateness
of the productivity adjustment; however, we are required pursuant to
section 1886(s)(2)(A)(i) of the Act to apply the specific productivity
adjustment described here. Because that provision specifically requires
application of the productivity adjustment, we do not believe section
1886(s) of the Act permits the Secretary discretion to remove it from
the calculation of the market basket update.
Comment: Commenters noted that CMS has underestimated the IPF
market basket increase over the last several years. They encouraged CMS
to utilize its exceptions and adjustments authority to apply a one-time
adjustment to course correct for its significantly lower estimates of
costs for FYs 2021 through 2023. They stated that failing to correct
CMS's gross underestimation of the payment updates during the pandemic
will further perpetuate inaccuracies in the payment rate moving
forward, resulting in a permanent cut to IPF payments.
Response: The IPF market basket updates are set prospectively,
which means that the update relies on a mix of both historical data for
part of the period for which the update is calculated and forecasted
data for the remainder. For instance, the FY 2024 market basket update
in this final rule reflects historical data through the first quarter
of CY 2023 and forecasted data through the third quarter of CY 2024.
While there is no precedent to adjust for market basket forecast error
in the IPF payment update, a forecast error can be calculated by
comparing the actual market basket increase for a given year less the
forecasted market basket increase. Due to the uncertainty regarding
future price trends, forecast errors can be both positive and negative.
Regarding the comment that the IPF market basket increase over the last
several years has been underestimated, we disagree with this assertion,
as from 2012 through 2020, the forecasted market basket updates for
each payment year for IPFs were higher than the actual market basket
updates. For this final rule, we have incorporated more recent
historical data and forecasts to capture the price and wage pressures
facing IPFs. We believe IGI's second quarter 2023 forecast of the FY
2024 percentage increase in the 2021-based IPF market basket is the
best available projection of inflation to determine the applicable
percentage increase for the IPF payments in FY 2024.
Final Decision: After consideration of public comments, we are
finalizing a FY 2024 IPF payment rate update of 3.3 percent (3.5
percent IPF market basket percentage increase reduced by the 0.2
percentage point productivity adjustment).
5. Labor-Related Share for FY 2024
Due to variations in geographic wage levels and other labor-related
costs, we believe that payment rates under the IPF PPS should continue
to be adjusted by a geographic wage index, which applies to the labor-
related portion of the Federal per diem base rate (hereafter referred
to as the labor-related share). The labor-related share is determined
by identifying the national average proportion of total costs that are
related to, influenced by, or vary with the local labor market. We
proposed to continue to classify a cost category as labor-related if
the costs are labor-intensive and vary with the local labor market.
We proposed to include in the labor-related share the sum of the
relative importance of the following cost categories: Wages and
Salaries, Employee Benefits, Professional Fees: Labor-Related,
Administrative and Facilities Support Services, Installation,
Maintenance, and Repair Services, All Other: Labor-Related Services,
and a portion of the Capital-Related cost weight from the 2021-based
IPF market basket. These are the same categories as the 2016-based IPF
market basket.
Similar to the 2016-based IPF market basket, the 2021-based IPF
market basket includes two cost categories for nonmedical Professional
fees (including but not limited to, expenses for legal, accounting, and
engineering services). These are Professional Fees: Labor-Related and
Professional Fees: Nonlabor-Related. For the 2021-based IPF market
basket, we proposed to estimate the labor-related percentage of non-
medical professional fees (and assign these expenses to the
Professional Fees: Labor-Related services cost category) based on the
same method that was used to determine the labor-related percentage of
professional fees in the 2016-based IPF market basket.
As was done in the 2016-based IPF market basket, we proposed to
determine the proportion of legal, accounting and auditing,
engineering, and management consulting services that meet our
definition of labor-related services based on a survey of hospitals
conducted by CMS in 2008. We notified the public of our intent to
conduct this survey on December 9, 2005, (70 FR 73250) and did not
receive any public comments in response to the notice (71 FR 8588). A
discussion of the composition of the survey and post-stratification can
be found in the FY 2010 IPPS/LTCH PPS final rule (74 FR 43850 through
43856). Based on the weighted results of the survey, we determined that
hospitals purchase, on average, the following portions of contracted
professional services outside of their local labor market:
34 percent of accounting and auditing services.
30 percent of engineering services.
33 percent of legal services.
42 percent of management consulting services.
We proposed to apply each of these percentages to the respective
2012 Benchmark I-O cost category underlying the professional fees cost
category to determine the Professional Fees: Nonlabor-Related costs.
The Professional Fees: Labor-Related costs were determined to be the
difference between the total costs for each Benchmark I-O category and
the Professional Fees: Nonlabor-Related costs. This is the same
methodology that we used to separate the 2016-based IPF market basket
professional fees category into Professional Fees: Labor-Related and
Professional Fees: Nonlabor-Related cost categories (84 FR 38445).
Effective for transmittal 18, (https://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/Transmittals/r18p240i) the hospital
Medicare cost report (CMS Form 2552-10, OMB No. 0938-0050) is
collecting information on whether a hospital purchased professional
services (for example, legal, accounting, tax preparation, bookkeeping,
payroll, advertising, and/or management/consulting services) from an
unrelated organization and if the majority of these expenses were
purchased from unrelated organizations located outside of the main
hospital's local area labor market. We encourage all providers to
provide this information so we can potentially use these data in future
[[Page 51079]]
rulemaking to determine the labor-related share.
In the 2021-based IPF market basket, nonmedical professional fees
that were subject to allocation based on these survey results represent
3.3 percent of total costs (and are limited to those fees related to
Accounting & Auditing, Legal, Engineering, and Management Consulting
services). Based on our survey results, we proposed to apportion 2.1
percentage points of the 3.3 percentage point figure into the
Professional Fees: Labor-Related share cost category and designate the
remaining 1.2 percentage point into the Professional Fees: Nonlabor-
Related cost category.
In addition to the professional services listed, for the 2021-based
IPF market basket, we proposed to allocate a proportion of the Home
Office/Related Organization Contract Labor cost weight, calculated
using the Medicare cost reports, into the Professional Fees: Labor-
Related and Professional Fees: Nonlabor-Related cost categories. We
proposed to classify these expenses as labor-related and nonlabor-
related, as many facilities are not located in the same geographic area
as their home office and, therefore, do not meet our definition for the
labor-related share, which requires the services to be purchased in the
local labor market.
Similar to the 2016-based IPF market basket, we proposed for the
2021-based IPF market basket to use the Medicare cost reports for both
freestanding IPF providers and hospital-based IPF providers to
determine the home office labor-related percentages. The Medicare cost
report requires a hospital to report information regarding its home
office provider. Using information on the Medicare cost report, we then
compare the location of the IPF with the location of the IPF's home
office. We proposed to classify an IPF with a home office located in
its respective labor market if the IPF and its home office are located
in the same metropolitan statistical area (MSA). We then determine the
proportion of the Home Office/Related Organization Contract Labor cost
weight that should be allocated to the labor-related share based on the
percent of total Medicare allowable costs for those IPFs that had home
offices located in their respective local labor markets of total
Medicare allowable costs for IPFs with a home office. We determined an
IPF's and its home office's MSA using their zip code information from
the Medicare cost report. Using this methodology, we determined that 46
percent of IPFs' Medicare allowable costs were for home offices located
in their respective local labor markets. Therefore, we are allocating
46 percent of the Home Office/Related Organization Contract Labor cost
weight (2.1 percentage points = 4.7 percent times 46 percent) to the
Professional Fees: Labor-Related cost weight and 54 percent of the Home
Office/Related Organization Contract Labor cost weight to the
Professional Fees: Nonlabor-Related cost weight (2.5 percentage points
= 4.7 percent times 54 percent). The same methodology was used for the
2016-based IPF market basket (84 FR 38445).
In summary, we apportioned 2.1 percentage points of the non-medical
professional fees and 2.1 percentage points of the Home Office/Related
Organization Contract Labor cost weight into the Professional Fees:
Labor-Related cost category. This amount was added to the portion of
professional fees that we already identified as labor-related using the
I-O data such as contracted advertising and marketing costs
(approximately 0.5 percentage point of total costs), resulting in a
Professional Fees: Labor-Related cost weight of 4.7 percent.
Comment: One commenter appreciated CMS's proposal to increase the
labor-related share based on data that better reflects increased labor
costs as a percentage of an IPF's overall cost structure. However, they
disagreed with CMS's proposal to exclude from the labor-related share
the proportion of non-medical professional services fees presumed to
have been purchased outside of the hospital's labor market. The
commenter disagreed with CMS's assertion/assumption that services
purchased from national firms are not affected by the local labor
market. The commenter stated that when hospitals seek professional
services, the services they are seeking (such as, accounting,
engineering, or management consulting) typically are not so unique that
they could only be provided by regional or national firms. The
commenter stated that CMS's own survey data support this conclusion, as
approximately 64 percent of these services are sourced from firms in
the local market. The commenter stated that costs of services purchased
from firms outside the hospital's labor market should be included with
the labor-related share of costs.
The commenter requested that CMS provide evidence that pricing for
professional services provided by regional and national firms to
hospitals is offered in a national market that is not subject to
geographic cost variation. The commenter urged that, unless the agency
can produce strong evidence that prices for professional services
provided by firms outside of a hospital's local labor market are
homogenous, CMS restore the 1.2 percentage points it proposed to
reclassify to Professional Services: Nonlabor-Related to the
Professional Services: Labor-Related category.
Response: We respectfully disagree with the commenter and continue
to believe it is appropriate that a proportion of Accounting &
Auditing, Legal, Engineering, and Management Consulting services costs
purchased by hospitals should be excluded from the labor-related share.
As discussed in the RY 2007 IPF PPS final rule (71 FR 27061), RY
2009 IPF PPS (73 FR 25719) and the RY 2010 IPF PPS notices (74 FR
20373), to provide an adjustment for geographic wage levels, the labor-
related portion of an IPF's payment is adjusted using an appropriate
wage index. The purpose of the labor-related share is to reflect the
proportion of the national PPS base payment rate that is adjusted by
the hospital's wage index (representing the relative costs of their
local labor market to the national average). Therefore, we include a
cost category in the labor-related share if the costs are labor-
intensive and vary with the local labor market.
As acknowledged by the commenter and confirmed by the survey of
hospitals conducted by CMS in 2008 (as stated above), professional
services can be purchased from local firms as well as national and
regional professional services firms. It is not necessarily the case,
as asserted by the commenter, that these national and regional firms
have fees that match those in the local labor market even though
providers have the option to utilize those firms. That is, fees for
services purchased from firms outside the local labor market may differ
from those that would be purchased in the local labor market for any
number of reasons (including but not limited to, the skill level of the
contracted personnel, higher capital costs, etc.). As noted earlier in
this section of this final rule, the definition for the labor-related
share requires the services to be purchased in the local labor market;
therefore, CMS's allocation of approximately 64 percent of the
Professional Fees cost weight allocated to the Professional Fees:
Labor-Related cost weight based on the 2008 survey results \2\ is
consistent with the commenter's assertion that not all Professional
Fees services are purchased
[[Page 51080]]
in the local labor market. We believe it is reasonable to conclude that
costs of those professional services purchased directly within the
local labor market are directly related to local labor market
conditions (which are reflected in the IPF's respective wage index)
and, thus, should be included in the labor-related share. The remaining
approximately 36 percent of Professional Fees costs which are purchased
outside the local labor market reflects different and additional
factors outside the local labor market and, thus, should be excluded
from the labor-related share. In addition, we note the compensation
costs of professional services provided by hospital employees (which
would reflect the local labor market) are included in the labor-related
share, as they are included in the Wages and Salaries and Benefit cost
weights.
---------------------------------------------------------------------------
\2\ The 64 percent value is based on a survey conducted by CMS
in 2008 as detailed in the FY 2010 IPPS/LTCH PPS final rule (74 FR
43850 through 43856). This was also used to determine the
Professional Fees: Labor-Related cost weight in the 2016-based IPF
market basket.
---------------------------------------------------------------------------
Therefore, for the reasons discussed, we believe our proposed
methodology of allocating only a portion of Professional Fees to the
Professional Fees: Labor-Related cost category is appropriate. As
stated previously, effective for transmittal 18 (https://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/Transmittals/r18p240i),
the hospital Medicare Cost Report (CMS Form 2552-10, OMB No. 0938-0050)
is collecting information on whether a hospital purchased professional
services (for example, legal, accounting, tax preparation, bookkeeping,
payroll, advertising, and/or management/consulting services) from an
unrelated organization and if the majority of these expenses were
purchased from unrelated organizations located outside of the main
hospital's local area labor market. We encourage all providers to
provide this information for potential use in future rulemaking to
determine the labor-related share.
Comment: One commenter did not support the proposed increase to the
labor-related share. This commenter stated that any increase to the
labor-related share percentage penalizes any facility that has a wage
index less than 1.0. The commenter further stated that across the
country, there is a growing disparity between high-wage and low-wage
states that harms hospitals in many rural and underserved communities.
The commenter stated that limiting the increase in the labor-related
share would help mitigate that growing disparity and recommended that
CMS consider excluding the labor portion of capital-related costs for
FY 2024 and going forward.
Response: As discussed in section IV.D.1.a, the IPF PPS wage index
is applied to the labor-related portion of an IPF's payment to provide
an adjustment for geographic wage levels. The methodology to use the
relative importance values for the labor-related cost categories from
the most recent IPF market basket is consistent with the determination
of the labor-related share since the implementation of the IPF PPS in
2007. The labor-related cost categories reflect IPF costs that are
related to, influenced by, or vary with the local labor market, which
would include a portion of the capital-related costs since the
construction costs for capital infrastructure would be influenced by
the local labor market. Therefore, we disagree with the commenter that
we should exclude the labor portion of capital-related costs for FY
2024 and going forward.
Comment: One commenter disagreed with the assumption that home
office compensation costs that occur outside of a hospital's labor
market are not subject to geographic wage variation and stated that
they do not believe that the proposed reclassification to the
Professional Fees: Non-Labor-Related cost category is justified. The
commenters stated that the proposed methodology fails to consider that
the home office is essentially a part of the hospital, and thus the
hospital, along with its home office, is operating in multiple labor
markets. The commenters stated that the home office's portion of the
hospital's labor costs should not be excluded from the labor-related
share simply because they are not in the same labor market as the
hospital.
The commenter conducted their own analysis of the Medicare cost
report data showing that providers with a home office outside of their
local labor market had wage indexes both below 1 as well as greater
than 1. The commenter stated that those hospitals in a labor market
with a wage index greater than 1 had mean home office average hourly
wage costs that were greater than the mean home office average hourly
wage costs of those hospitals in a labor market with a wage index less
than 1. The commenter claimed that these data indicate that, contrary
to CMS' assertion, home office salary, wage, and benefit costs for
hospitals with home offices outside of their labor market are subject
to geographic wage variation. The commenter requested that CMS allocate
the full 4.7 percentage points of the Home Office/Related Organization
cost weight to the labor-related share.
Response: As discussed in the RY 2007 IPF PPS final rule (71 FR
27061), RY 2009 IPF PPS (73 FR 25719) and the RY 2010 IPF PPS notices
(74 FR 20373), to provide an adjustment for geographic wage levels, the
labor-related portion of an IPF's payment is adjusted using an
appropriate wage index. Due to the variation in costs and because of
the differences in geographic wage levels, in the November 15, 2004 IPF
PPS final rule, we required that payment rates under the IPF PPS be
adjusted by a geographic wage index. We proposed and finalized a policy
to use the unadjusted, pre-floor, pre-reclassified IPPS hospital wage
index (representing the wage level in the geographic area of the
hospital compared to the national average hospital wage level as
specified under Section 1886(d)(3)(E)) to account for geographic
differences in IPF labor costs. Therefore, consistent with the
definition of labor-related share used for IPPS hospitals, we have
included a cost category in the labor-related share for IPFs if the
costs are labor-intensive and vary with the local labor market (that
is, the geographic area of the hospital).
As the commenter stated, and as validated with the Medicare cost
report data, a hospital's home office can be located outside the
hospital's local labor market. For other types of professional
services, we only include the costs for services purchased directly
within the geographic area of the hospital in the labor-related share
because they reflect the local labor market conditions that are
consistent with the intent of the geographic adjustment. We believe it
is reasonable to conclude that costs of those home office services
purchased directly within the geographic area of the hospital should
also be included in the labor-related share because they are impacted
by local labor market conditions. As we have previously discussed in
the RY 2007 final rule (71 FR 27066), we believe that the actual
location of an IPF (as opposed to the location of affiliated providers)
is most appropriate for determining the wage adjustment, because the
prevailing wages in the area in which the IPF is located influence the
cost of a case. And as we do for professional services, we believe home
office costs that are not in the same geographic area as the hospital
should be excluded from the labor-related share because they are
influenced by factors outside of the hospital's local labor market. To
implement this approach, we proposed a methodology that relies on the
Medicare cost report data for hospitals reporting home office
information to determine whether their home office is in the same
geographic area of the hospital (which we define as the hospital's
Metropolitan Statistical Area). Our methodology determined that 46
percent of the Home Office/Related Organization cost weight (reflecting
compensation costs) are associated with
[[Page 51081]]
the geographic area of the hospital, whereas the remaining 54 percent
of home office costs are purchased outside the geographic area of the
hospital. Therefore, we believe our proposed methodology of only
allocating the portion of the Home Office/Related Organization cost
weight (46 percent) into the Professional Fees: Labor-Related cost
weight that are purchased in the same geographic area as the hospital
is appropriate as it is consistent with the intent of the geographic
adjustment. In addition, we note that the compensation costs for
hospital employees, which would reflect the local labor market
performing the same tasks as home office personnel are included in the
labor-related share as they are included in the Wages and Salaries and
Employee Benefits cost weights.
As stated, we proposed to include in the labor-related share the
sum of the relative importance of Wages and Salaries, Employee
Benefits, Professional Fees: Labor-Related, Administrative and
Facilities Support Services, Installation, Maintenance, and Repair
Services, All Other: Labor-Related Services, and a portion of the
Capital-Related cost weight from the 2021-based IPF market basket, as
this meets our definition of the labor-related share with costs that
are labor intensive and vary with the local labor market.
Final Decision: After consideration of public comments, we are
finalizing the 2021-based IPF market basket proposed labor-related cost
categories and base year cost weights as proposed.
We also proposed that if more recent data were subsequently
available, we would use such data to determine the FY 2024 labor-
related share in the final rule. Based on IGI's second quarter 2023
forecast for the 2021-based IPF market basket, the sum of the FY 2024
relative importance for Wages and Salaries, Employee Benefits,
Professional Fees: Labor-Related, Administrative and Facilities Support
Services, Installation Maintenance & Repair Services, and All Other:
Labor-Related Services is 75.6 percent. The portion of Capital-Related
costs that is influenced by the local labor market is estimated to be
46 percent, which is the same percentage applied to the 2016-based IPF
market basket (84 FR 38446 through 38447). Since the relative
importance for Capital-Related costs is 6.8 percent of the 2021-based
IPF market basket in FY 2024, we took 46 percent of 6.8 percent to
determine the labor-related share of Capital-Related costs for FY 2024
of 3.1 percent. Therefore, the total labor-related share for FY 2024
based on more recent data is 78.7 percent (the sum of 75.6 percent for
the operating costs and 3.1 percent for the labor-related share of
Capital-Related costs). Table 15 shows the FY 2024 labor-related share
using the 2021-based IPF market basket relative importance and the FY
2023 labor-related share using the 2016-based IPF market basket.
[GRAPHIC] [TIFF OMITTED] TR02AU23.016
The FY 2024 labor-related share using the 2021-based IPF market
basket is about 1.0 percentage point higher than the FY 2023 labor-
related share using the 2016-based IPF market basket. This higher
labor-related share is primarily due to the incorporation of the 2021
Medicare cost report data, which increased the Compensation cost weight
by 0.9 percentage point compared to the 2016-based IPF market basket,
as shown in Table 1 and Table 2 in section IV.A.3.a.(2) of this final
rule.
B. Updates to the IPF PPS Rates for FY Beginning October 1, 2023
The IPF PPS is based on a standardized Federal per diem base rate
calculated from the IPF average per diem costs and adjusted for budget
neutrality in the implementation year. The Federal per diem base rate
is used as the standard payment per day under the IPF PPS and is
adjusted by the patient-level and facility-level adjustments that are
applicable to the IPF stay. A detailed explanation of how we calculated
the average per diem cost appears in the November 2004 IPF PPS final
rule (69 FR 66926).
[[Page 51082]]
1. Determining the Standardized Budget-Neutral Federal Per Diem Base
Rate
Section 124(a)(1) of the BBRA required that we implement the IPF
PPS in a budget-neutral manner. In other words, the amount of total
payments under the IPF PPS, including any payment adjustments, must be
projected to be equal to the amount of total payments that would have
been made if the IPF PPS were not implemented. Therefore, we calculated
the budget neutrality factor by setting the total estimated IPF PPS
payments to be equal to the total estimated payments that would have
been made under the Tax Equity and Fiscal Responsibility Act of 1982
(TEFRA) (Pub. L. 97-248) methodology had the IPF PPS not been
implemented. A step-by-step description of the methodology used to
estimate payments under the Tax Equity and Fiscal Responsibility Act
(TEFRA) payment system appears in the November 2004 IPF PPS final rule
(69 FR 66926).
Under the IPF PPS methodology, we calculated the final Federal per
diem base rate to be budget-neutral during the IPF PPS implementation
period (that is, the 18-month period from January 1, 2005, through June
30, 2006) using a July 1 update cycle. We updated the average cost per
day to the midpoint of the IPF PPS implementation period (October 1,
2005), and this amount was used in the payment model to establish the
budget-neutrality adjustment.
Next, we standardized the IPF PPS Federal per diem base rate to
account for the overall positive effects of the IPF PPS payment
adjustment factors by dividing total estimated payments under the TEFRA
payment system by estimated payments under the IPF PPS. The information
concerning this standardization can be found in the November 2004 IPF
PPS final rule (69 FR 66932) and the RY 2006 IPF PPS final rule (71 FR
27045). We then reduced the standardized Federal per diem base rate to
account for the outlier policy, the stop loss provision, and
anticipated behavioral changes. A complete discussion of how we
calculated each component of the budget neutrality adjustment appears
in the November 2004 IPF PPS final rule (69 FR 66932 through 66933) and
in the RY 2007 IPF PPS final rule (71 FR 27044 through 27046). The
final standardized budget-neutral Federal per diem base rate
established for cost reporting periods beginning on or after January 1,
2005, was calculated to be $575.95.
The Federal per diem base rate has been updated in accordance with
applicable statutory requirements and Sec. 412.428 through publication
of annual notices or proposed and final rules. A detailed discussion on
the standardized budget-neutral Federal per diem base rate and the ECT
payment per treatment appears in the FY 2014 IPF PPS update notice (78
FR 46738 through 46740). These documents are available on the CMS
website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/.
IPFs must include a valid procedure code for ECT services provided
to IPF beneficiaries in order to bill for ECT services, as described in
our Medicare Claims Processing Manual, Chapter 3, Section 190.7.3
(available at https://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/Downloads/clm104c03.pdf.) There were no changes to the ECT
procedure codes used on IPF claims as a result of the final update to
the ICD-10-PCS code set for FY 2024. Addendum B to this final rule
shows the ECT procedure codes for FY 2024 and is available on our
website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/tools.html.
2. Update of the Federal Per Diem Base Rate and Electroconvulsive
Therapy Payment Per Treatment
The current (FY 2023) Federal per diem base rate is $865.63, and
the ECT payment per treatment is $372.67. For the final FY 2024 Federal
per diem base rate, we applied the payment rate update of 3.3 percent--
that is, the 2021-based IPF market basket increase for FY 2024 of 3.5
percent less the productivity adjustment of 0.2 percentage point--and
the wage index budget-neutrality factor of 1.0016 (as discussed in
section IV.D.1 of this final rule) to the FY 2023 Federal per diem base
rate of $865.63, yielding a final Federal per diem base rate of $895.63
for FY 2024. Similarly, we applied the 3.3 percent payment rate update
and the 1.0016 wage index budget-neutrality factor to the FY 2023 ECT
payment per treatment of $372.67, yielding a final ECT payment per
treatment of $385.58 for FY 2024.
Section 1886(s)(4)(A)(i) of the Act requires that for RY 2014 and
each subsequent RY, in the case of an IPF that fails to report required
data under the IPFQR Program with respect to such RY, the Secretary
will reduce any annual update to a standard federal rate for discharges
during the RY by 2.0 percentage points. Therefore, we are applying a
2.0 percentage points reduction to the Federal per diem base rate and
the ECT payment per treatment as follows:
For IPFs that fail requirements under the IPFQR Program,
we applied a 1.3 percent payment rate update--that is, the IPF market
basket increase for FY 2024 of 3.5 percent less the productivity
adjustment of 0.2 percentage point for an update of 3.3 percent, and
further reduced by 2.0 percentage points in accordance with section
1886(s)(4)(A)(i) of the Act--and the wage index budget-neutrality
factor of 1.0016 to the FY 2023 Federal per diem base rate of $865.63,
yielding a Federal per diem base rate of $878.29 for FY 2024.
For IPFs that fail to meet requirements under the IPFQR
Program, we applied a 1.3 percent annual payment rate update and a
1.0016 wage index budget-neutrality factor to the FY 2023 ECT payment
per treatment of $372.67 yielding an ECT payment per treatment of
$378.12 for FY 2024. Lastly, we proposed that if more recent data
became available, we would use such data, if appropriate, to determine
the FY 2024 Federal per diem base rate and ECT payment per treatment
for the final rule.
Finally, we note that in the April 10, 2023 IPF PPS proposed rule
(88 FR 21259), there were two technical errors in describing the
calculation of the FY 2024 proposed base rate and electroconvulsive
therapy (ECT) payment per treatment for IPFs that fail to meet
requirements under the Inpatient Psychiatric Facility Quality Reporting
(IPFQR) Program. In describing the calculation of the FY 2024 Federal
per diem base rate for IPFs that fail to meet requirements under the
IPFQR Program, we inadvertently stated that we applied the market
basket update, reduced by 2.0 percentage points to the FY 2024 Federal
per diem base rate and FY 2024 ECT payment per treatment. In accordance
with our longstanding methodology, and with the actual calculation of
these proposed payment updates, the description of these calculations
should have used the FY 2023 Federal per diem rate and FY 2023 ECT
payment per treatment rather than the FY 2024 Federal per diem rate and
ECT payment per treatment. To be clear, these errors only affected the
description of the starting values from which the rates were
calculated, and the calculations themselves, as well as the rates
indicated in the proposed rule, were correct and consistent with our
longstanding methodology for updating the IPF Federal per diem base
rate and ECT payment per treatment.
[[Page 51083]]
C. Updates to the IPF PPS Patient-Level Adjustment Factors
1. Overview of the IPF PPS Adjustment Factors
The IPF PPS payment adjustments were derived from a regression
analysis of 100 percent of the FY 2002 Medicare Provider and Analysis
Review (MedPAR) data file, which contained 483,038 cases. For a more
detailed description of the data file used for the regression analysis,
see the November 2004 IPF PPS final rule (69 FR 66935 through 66936).
We proposed to use the existing regression-derived adjustment factors
established in 2005 for FY 2024. However, we have used more recent
claims data to simulate payments to finalize the outlier fixed dollar
loss threshold amount and to assess the impact of the IPF PPS updates.
2. IPF PPS Patient-Level Adjustments
The IPF PPS includes payment adjustments for the following patient-
level characteristics: Medicare Severity Diagnosis Related Groups (MS-
DRGs) assignment of the patient's principal diagnosis, selected
comorbidities, patient age, and the variable per diem adjustments.
a. Update to MS-DRG Assignment
We believe it is important to maintain for IPFs the same diagnostic
coding and Diagnosis Related Group (DRG) classification used under the
IPPS for providing psychiatric care. For this reason, when the IPF PPS
was implemented for cost reporting periods beginning on or after
January 1, 2005, we adopted the same diagnostic code set (ICD-9-CM) and
DRG patient classification system (MS-DRGs) that were utilized at the
time under the IPPS. In the RY 2009 IPF PPS notice (73 FR 25709), we
discussed CMS's effort to better recognize resource use and the
severity of illness among patients. CMS adopted the new MS-DRGs for the
IPPS in the FY 2008 IPPS final rule with comment period (72 FR 47130).
In the RY 2009 IPF PPS notice (73 FR 25716), we provided a crosswalk to
reflect changes that were made under the IPF PPS to adopt the new MS-
DRGs. For a detailed description of the mapping changes from the
original DRG adjustment categories to the current MS-DRG adjustment
categories, we refer readers to the RY 2009 IPF PPS notice (73 FR
25714).
The IPF PPS includes payment adjustments for designated psychiatric
DRGs assigned to the claim based on the patient's principal diagnosis.
The DRG adjustment factors were expressed relative to the most
frequently reported psychiatric DRG in FY 2002, that is, DRG 430
(psychoses). The coefficient values and adjustment factors were derived
from the regression analysis discussed in detail in the November 28,
2003 IPF PPS proposed rule (68 FR 66923; 66928 through 66933) and the
November 15, 2004 IPF PPS final rule (69 FR 66933 through 66960).
Mapping the DRGs to the MS-DRGs resulted in the current 17 IPF MS-DRGs,
instead of the original 15 DRGs, for which the IPF PPS provides an
adjustment. For FY 2024, we did not propose any changes to the IPF MS-
DRG adjustment factors. Therefore, we are retaining the existing IPF
MS-DRG adjustment factors.
In the FY 2015 IPF PPS final rule published August 6, 2014, in the
Federal Register titled, ``Inpatient Psychiatric Facilities Prospective
Payment System--Update for FY Beginning October 1, 2014 (FY 2015)'' (79
FR 45945 through 45947), we finalized conversions of the ICD-9-CM-based
MS-DRGs to ICD-10-CM/PCS-based MS-DRGs, which were implemented on
October 1, 2015. As discussed in the FY 2015 IPF PPS proposed rule (79
FR 26047) in more detail, every year, changes to the ICD-10-CM and the
ICD-10-PCS coding system are addressed in the IPPS proposed and final
rules. The changes to the codes are effective October 1 of each year
and must be used by acute care hospitals as well as other providers to
report diagnostic and procedure information. In accordance with Sec.
412.428(e), the IPF PPS has always incorporated ICD-10-CM and ICD-10-
PCS coding changes made in the annual IPPS update and will continue to
do so. We will continue to publish coding changes in a Transmittal/
Change Request, similar to how coding changes are announced by the IPPS
and LTCH PPS. The coding changes relevant to the IPF PPS are also
published in the IPF PPS proposed and final rules, or in IPF PPS update
notices. Further information on the ICD-10-CM/PCS MS-DRG conversion
project can be found on the CMS ICD-10-CM website at https://www.cms.gov/Medicare/Coding/ICD10/ICD-10-MS-DRG-Conversion-Project.html.
For FY 2024, we proposed to continue making the existing payment
adjustment for psychiatric diagnoses that group to one of the existing
17 IPF MS-DRGs listed in Addendum A. Addendum A is available on our
website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/tools.html.. Psychiatric principal
diagnoses that do not group to one of the 17 designated MS-DRGs will
still receive the Federal per diem base rate and all other applicable
adjustments, but the payment will not include an MS-DRG adjustment.
As we did not propose any changes to the IPF MS-DRG adjustment
factors, we are retaining the existing IPF MS-DRG adjustment factors
for FY 2024.
The diagnoses for each IPF MS-DRG will be updated as of October 1,
2023, using the final FY 2024 IPPS ICD-10-CM/PCS code sets. The FY 2024
IPPS/LTCH PPS final rule will include tables of the changes to the ICD-
10-CM/PCS code sets, which underlie the FY 2024 IPF MS-DRGs. Both the
FY 2024 IPPS final rule and the tables of final changes to the ICD-10-
CM/PCS code sets, which underlie the FY 2024 MS-DRGs, will be available
on the CMS IPPS website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/AcuteInpatientPPS/.
Code First
As discussed in the ICD-10-CM Official Guidelines for Coding and
Reporting, certain conditions have both an underlying etiology and
multiple body system manifestations due to the underlying etiology. For
such conditions, the ICD-10-CM has a coding convention that requires
the underlying condition be sequenced first followed by the
manifestation. Wherever such a combination exists, there is a ``use
additional code'' note at the etiology code, and a ``code first'' note
at the manifestation code. These instructional notes indicate the
proper sequencing order of the codes (etiology followed by
manifestation). In accordance with the ICD-10-CM Official Guidelines
for Coding and Reporting, when a primary (psychiatric) diagnosis code
has a ``code first'' note, the provider will follow the instructions in
the ICD-10-CM Tabular List. The submitted claim goes through the CMS
processing system, which will identify the principal diagnosis code as
non-psychiatric and search the secondary codes for a psychiatric code
to assign a DRG code for adjustment. The system will continue to search
the secondary codes for those that are appropriate for comorbidity
adjustment.
For more information on the code first policy, we refer our readers
to the November 2004 IPF PPS final rule (69 FR 66945), and see sections
I.A.13 and I.B.7 of the FY 2020 ICD-10-CM Coding Guidelines, available
at https://www.cdc.gov/nchs/data/icd/10cmguidelines-FY2020_final.pdf.
In the FY 2015 IPF PPS final rule, we provided a code first table for
reference that highlights the same or similar manifestation codes where
the code first
[[Page 51084]]
instructions apply in ICD-10-CM that were present in ICD-10-CM (79 FR
46009). In FY 2018, FY 2019 and FY 2020, there were no changes to the
final ICD-10-CM codes in the IPF Code First table. For FY 2021 and FY
2022, there were 18 ICD-10-CM codes deleted from the final IPF Code
First table. For FY 2023, there were 2 ICD-10-CM codes deleted and 48
ICD-10-CM codes added to the IPF Code First table.
For FY 2024, there were no proposed changes to the Code First
Table. For this final rule, we are finalizing the deletion of 1 ICD-10-
CM code and the addition of 5 ICD-10-CM codes as ``code first'' codes.
There are 26 codes whose ``code first'' codes are being updated in the
IPF Code First Table to reflect these changes In accordance with our
longstanding practice for the IPF PPS and with Sec. 412.428(e), we are
adopting these latest ICD-10-CM changes for October, 2023 and
describing these changes in this FY 2024 IPF PPS final rule. The FY
2024 Code First table is shown in Addendum B on the CMS website at
https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/tools.html.
b. Payment for Comorbid Conditions
The intent of the comorbidity adjustments is to recognize the
increased costs associated with comorbid conditions by providing
additional payments for certain existing medical or psychiatric
conditions that are expensive to treat. In our RY 2012 IPF PPS final
rule (76 FR 26451 through 26452), we explained that the IPF PPS
includes 17 comorbidity categories and identified the new, revised, and
deleted ICD-9-CM diagnosis codes that generate a comorbid condition
payment adjustment under the IPF PPS for RY 2012 (76 FR 26451).
Comorbidities are specific patient conditions that are secondary to
the patient's principal diagnosis and that require treatment during the
stay. Diagnoses that relate to an earlier episode of care and have no
bearing on the current hospital stay are excluded and must not be
reported on IPF claims. Comorbid conditions must exist at the time of
admission or develop subsequently, and affect the treatment received,
LOS, or both treatment and LOS.
For each claim, an IPF may receive only one comorbidity adjustment
within a comorbidity category, but it may receive an adjustment for
more than one comorbidity category. Current billing instructions for
discharge claims, on or after October 1, 2015, require IPFs to enter
the complete ICD-10-CM codes for up to 24 additional diagnoses if they
co-exist at the time of admission, or develop subsequently and impact
the treatment provided.
The comorbidity adjustments were determined based on the regression
analysis using the diagnoses reported by IPFs in FY 2002. The principal
diagnoses were used to establish the DRG adjustments and were not
accounted for in establishing the comorbidity category adjustments,
except where ICD-9-CM code first instructions applied. In a code first
situation, the submitted claim goes through the CMS processing system,
which will identify the principal diagnosis code as non-psychiatric and
search the secondary codes for a psychiatric code to assign an MS-DRG
code for adjustment. The system will continue to search the secondary
codes for those that are appropriate for comorbidity adjustment.
As noted previously, it is our policy to maintain the same
diagnostic coding set for IPFs that is used under the IPPS for
providing the same psychiatric care. The 17 comorbidity categories
formerly defined using ICD-9-CM codes were converted to ICD-10-CM/PCS
in our FY 2015 IPF PPS final rule (79 FR 45947 through 45955). The goal
for converting the comorbidity categories is referred to as
replication, meaning that the payment adjustment for a given patient
encounter is the same after ICD-10-CM implementation as it would be if
the same record had been coded in ICD-9-CM and submitted prior to ICD-
10-CM/PCS implementation on October 1, 2015. All conversion efforts
were made with the intent of achieving this goal. For FY 2024, we
proposed to use the same comorbidity adjustment factors in effect in FY
2023. The FY 2024 comorbidity adjustment factors are found in Addendum
A, available on the CMS website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/tools.html.
For FY 2024, we proposed to add 2 ICD-10-CM codes and remove 1 ICD-
10-CM code from the Chronic Renal Failure category. We did not receive
any comments on this proposal, and we are finalizing these changes as
proposed. In addition, we are adding 2 ICD-10-CM codes to the Chronic
Obstructive Pulmonary Disease category, 1 ICD-10-CM code to the
Infectious Disease category, 4 ICD-10-CM codes to the Poisoning
category, 6 ICD-10-PCS codes for the Oncology Treatment Procedure
category. For the Oncology Treatment Diagnosis Category, we are adding
12 ICD-10-CM codes and deleting 2 ICD-10-CM codes. Finally, for the
Acute Renal Failure Category, we are adding 1 ICD-10-CM code and
deleting 1 ICD-10_CM code. In accordance with our longstanding practice
for the IPF PPS and with Sec. 412.428(e), we are adopting these latest
ICD-10-CM changes for October, 2023 and describing these changes in
this FY 2024 IPF PPS final rule.
The FY 2024 comorbidity codes are shown in Addenda B, available on
the CMS website at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/tools.html.
In accordance with the policy established in the FY 2015 IPF PPS
final rule (79 FR 45949 through 45952), we reviewed all new FY 2024
ICD-10-CM codes to remove codes that were site ``unspecified'' in terms
of laterality from the FY 2024 ICD-10-CM/PCS codes in instances where
more specific codes are available. As we stated in the FY 2015 IPF PPS
final rule, we believe that specific diagnosis codes that narrowly
identify anatomical sites where disease, injury, or a condition exists
should be used when coding patients' diagnoses whenever these codes are
available. We finalized in the FY 2015 IPF PPS rule, that we will
remove site ``unspecified'' codes from the IPF PPS ICD-10-CM/PCS codes
in instances when laterality codes (site specified codes) are
available, as the clinician should be able to identify a more specific
diagnosis based on clinical assessment at the medical encounter. None
of the finalized additions to the FY 2024 ICD-10-CM/PCS codes were site
``unspecified'' by laterality; therefore, we are not removing any of
the new codes.
c. Patient Age Adjustments
As explained in the November 2004 IPF PPS final rule (69 FR 66922),
we analyzed the impact of age on per diem cost by examining the age
variable (range of ages) for payment adjustments. In general, we found
that the cost per day increases with age. The older age groups are
costlier than the under 45 age group, the differences in per diem cost
increase for each successive age group, and the differences are
statistically significant. For FY 2024, we proposed continuing to use
the patient age adjustments currently in effect for FY 2023, as shown
in Addendum A of this final rule (see https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/tools.html).
As we did not propose any changes to the patient age adjustment
factors, we are retaining the existing patient age adjustment factors
for FY 2024.
[[Page 51085]]
d. Variable Per Diem Adjustments
We explained in the November 2004 IPF PPS final rule (69 FR 66946)
that the regression analysis indicated that per diem cost declines as
the LOS increases. The variable per diem adjustments to the Federal per
diem base rate account for ancillary and administrative costs that
occur disproportionately in the first days after admission to an IPF.
As discussed in the November 2004 IPF PPS final rule, we used a
regression analysis to estimate the average differences in per diem
cost among stays of different lengths (69 FR 66947 through 66950). As a
result of this analysis, we established variable per diem adjustments
that begin on day 1 and decline gradually until day 21 of a patient's
stay. For day 22 and thereafter, the variable per diem adjustment
remains the same each day for the remainder of the stay. However, the
adjustment applied to day 1 depends upon whether the IPF has a
qualifying ED. If an IPF has a qualifying ED, it receives a 1.31
adjustment factor for day 1 of each stay. If an IPF does not have a
qualifying ED, it receives a 1.19 adjustment factor for day 1 of the
stay. The ED adjustment is explained in more detail in section IV.D.4
of this final rule.
For FY 2024, we proposed to use the variable per diem adjustment
factors currently in effect in FY 2023, as shown in Addendum A to this
final rule (available at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/tools.html). A complete
discussion of the variable per diem adjustments appears in the November
2004 IPF PPS final rule (69 FR 66946).
As we did not propose any changes to the variable per diem
adjustment factors, we are retaining the existing variable per diem
adjustment factors for FY 2024.
D. Updates to the IPF PPS Facility-Level Adjustments
The IPF PPS includes facility-level adjustments for the wage index,
IPFs located in rural areas, teaching IPFs, cost of living adjustments
for IPFs located in Alaska and Hawaii, and IPFs with a qualifying ED.
1. Wage Index Adjustment
a. Background
As discussed in the RY 2007 IPF PPS final rule (71 FR 27061), RY
2009 IPF PPS (73 FR 25719) and the RY 2010 IPF PPS notices (74 FR
20373), to provide an adjustment for geographic wage levels, the labor-
related portion of an IPF's payment is adjusted using an appropriate
wage index. Currently, an IPF's geographic wage index value is
determined based on the actual location of the IPF in an urban or rural
area, as defined in 42 CFR 412.64(b)(1)(ii)(A) and (C).
Due to the variation in costs and because of the differences in
geographic wage levels, in the November 15, 2004 IPF PPS final rule, we
required that payment rates under the IPF PPS be adjusted by a
geographic wage index. We proposed and finalized a policy to use the
unadjusted, pre-floor, pre-reclassified IPPS hospital wage index to
account for geographic differences in IPF labor costs. We implemented
use of the pre-floor, pre-reclassified IPPS hospital wage data to
compute the IPF wage index since there was not an IPF-specific wage
index available. We believe that IPFs generally compete in the same
labor market as IPPS hospitals, so the pre-floor, pre-reclassified IPPS
hospital wage data should be reflective of labor costs of IPFs. We
believe this pre-floor, pre-reclassified IPPS hospital wage index to be
the best available data to use as proxy for an IPF specific wage index.
As discussed in the RY 2007 IPF PPS final rule (71 FR 27061 through
27067), under the IPF PPS, the wage index is calculated using the IPPS
wage index for the labor market area in which the IPF is located,
without considering geographic reclassifications, floors, and other
adjustments made to the wage index under the IPPS. For a complete
description of these IPPS wage index adjustments, we refer readers to
the FY 2019 IPPS/LTCH PPS final rule (83 FR 41362 through 41390). Our
wage index policy at Sec. 412.424(a)(2), requires that we use the best
Medicare data available to estimate costs per day, including an
appropriate wage index to adjust for wage differences.
When the IPF PPS was implemented in the November 15, 2004 IPF PPS
final rule, with an effective date of January 1, 2005, the pre-floor,
pre-reclassified IPPS hospital wage index that was available at the
time was the FY 2005 pre-floor, pre-reclassified IPPS hospital wage
index. Historically, the IPF wage index for a given RY has used the
pre-floor, pre-reclassified IPPS hospital wage index from the prior FY
as its basis. This has been due in part to the pre-floor, pre-
reclassified IPPS hospital wage index data that were available during
the IPF rulemaking cycle, where an annual IPF notice or IPF PPS final
rule was usually published in early May. This publication timeframe was
relatively early compared to other Medicare payment rules, because the
IPF PPS follows a RY, which was defined in the implementation of the
IPF PPS as the 12-month period from July 1 to June 30 (69 FR 66927).
Therefore, the best available data at the time the IPF PPS was
implemented was the pre-floor, pre-reclassified IPPS hospital wage
index from the prior FY (for example, the RY 2006 IPF wage index was
based on the FY 2005 pre-floor, pre-reclassified IPPS hospital wage
index).
In the RY 2012 IPF PPS final rule, we changed the reporting year
timeframe for IPFs from a RY to the FY, which begins October 1 and ends
September 30 (76 FR 26434 through 26435). In that RY 2012 IPF PPS final
rule, we continued our established policy of using the pre-floor, pre-
reclassified IPPS hospital wage index from the prior year (that is,
from FY 2011) as the basis for the FY 2012 IPF wage index. This policy
of basing a wage index on the prior year's pre-floor, pre-reclassified
IPPS hospital wage index has been followed by other Medicare payment
systems, such as hospice and inpatient rehabilitation facilities. By
continuing with our established policy, we remained consistent with
other Medicare payment systems.
In FY 2020, we finalized the IPF wage index methodology to align
the IPF PPS wage index with the same wage data timeframe used by the
IPPS for FY 2020 and subsequent years. Specifically, we finalized to
use the pre-floor, pre-reclassified IPPS hospital wage index from the
FY concurrent with the IPF FY as the basis for the IPF wage index. For
example, the FY 2020 IPF wage index was based on the FY 2020 pre-floor,
pre-reclassified IPPS hospital wage index rather than on the FY 2019
pre-floor, pre-reclassified IPPS hospital wage index.
We explained in the FY 2020 proposed rule (84 FR 16973), that using
the concurrent pre-floor, pre-reclassified IPPS hospital wage index
will result in the most up-to-date wage data being the basis for the
IPF wage index. It will also result in more consistency and parity in
the wage index methodology used by other Medicare payment systems. The
Medicare SNF PPS already used the concurrent IPPS hospital wage index
data as the basis for the SNF PPS wage index. Thus, the wage adjusted
Medicare payments of various provider types will be based upon wage
index data from the same timeframe. CMS proposed similar policies to
use the concurrent pre-floor, pre-reclassified IPPS hospital wage index
data in other Medicare payment systems, such as hospice and inpatient
rehabilitation facilities. For FY 2024, we proposed to continue using
the concurrent pre-floor, pre-reclassified IPPS hospital wage
[[Page 51086]]
index as the basis for the IPF wage index.
We proposed to apply the IPF wage index adjustment to the labor-
related share of the national base rate and ECT payment per treatment.
The labor-related share of the national rate and ECT payment per
treatment would change from 77.4 percent in FY 2023 to 78.7 percent in
FY 2024. This percentage reflects the labor-related share of the 2021-
based IPF market basket for FY 2024 (see section IV.A of this final
rule).
Comment: Several commenters urged CMS to revise the IPF wage index
methodology. Specifically, a few commenters suggested CMS revise the
policy so that the post-reclassification and post-floor hospital IPPS
wage index is used to calculate the wage index for IPFs. The commenter
believes that the continued use of the pre-reclassification and pre-
floor hospital inpatient wage index is unreasonable because it places
IPFs at a disadvantage in the labor markets in which they operate
relative to hospitals in the same markets.
Other commenters suggested CMS exercise its authority to refine the
IPF PPS by applying the pre-floor, pre-reclassified IPPS hospital wage
index for the CBSA in which the nearest IPPS hospital is located where
the pre-floor, pre-classified IPPS hospital wage index for the CBSA in
which the IPF is located only includes data from a closed IPPS
hospital. Commenters stated they believe the closed hospital data is
more likely to be unreliable such that the application of the pre-
floor, pre-reclassified IPPS hospital wage index would result in an
inappropriately deflated wage index value. Commenters further asserted
that the closure of the only IPPS hospital in the CBSA would suggest
that the community is currently underserved, and would make it
particularly appropriate to ensure that aberrant wage index data does
not serve as an impediment to new IPF services in a community.
Response: We appreciate the commenters' recommendations. We did not
propose the specific policies suggested by commenters, but we will take
them into consideration to potentially inform future rulemaking. We do
not believe that the continued use of the pre-reclassification and pre-
floor hospital inpatient wage index for FY 2024 is unreasonable or that
this policy puts IPFs at a disadvantage relative to hospitals in the
labor markets in which they operate. As we have previously discussed in
the RY 2007 final rule (71 FR 27066), we believe that the actual
location of an IPF (as opposed to the location of affiliated providers)
is most appropriate for determining the wage adjustment, because the
prevailing wages in the area in which the IPF is located influence the
cost of a case. In that same RY 2007 final rule (71 FR 27066), we also
stated that we believe the ``rural floor'' is required only for the
acute care hospital payment system, because section 4410 of the
Balanced Budget Act of 1997 (Pub. L. 105-33) applies specifically to
acute care hospitals and not excluded hospitals and excluded units. As
we have previously discussed, the IPF wage index is intended to be a
relative measure of the value of labor in prescribed labor market areas
(87 FR 46857). There is a variety of reasons why our longstanding IPF
wage index policy has not applied floors or reclassifications, which as
we previously noted, are not applied to the IPF wage index by statute.
For example, applying floors and reclassifications to the IPF wage
index would significantly increase administrative burden, both for IPFs
and for CMS, that would be associated with IPFs reclassifying from one
CBSA to another, and it would significantly increase the complexity of
the methodology. Furthermore, because floors and reclassifications
would be applied budget-neutrally under the wage index, these policies
would increase the wage index for some IPFs while reducing IPF PPS
payments for all other IPFs, which would upset the long-settled
expectations with which IPFs across the country have been operating.
For these reasons, we believe using the pre-floor, pre-reclassified
IPPS hospital wage index is the most appropriate data to use as a proxy
for an IPF wage index.
Regarding the suggestion to apply the wage index for the CBSA of
the nearest IPPS hospital in cases when an IPF's CBSA includes only a
closed IPPS hospital, we disagree with the commenter that wage data
from a hospital that has subsequently closed is more likely to be
unreliable and that such data would inappropriately deflate the wage
index for that CBSA. Rather, following the longstanding methodology for
calculating the wage index, wage data from the period during which the
hospital was open would be comparable to wage data from the same period
for hospitals located in other geographical areas, and would provide an
appropriate relative measure of the value of labor in that CBSA's labor
market area compared to others. We do not believe that such wage data
or the wage index of a CBSA in this situation would serve as an
impediment for either new or existing IPF services in a community. In
addition, we recognize that in some cases, the closure of the only IPPS
hospital in the CBSA could suggest that the community is underserved;
however, in other cases, the lack of an IPPS hospital could be due to
other factors, such as when an area's only IPPS hospital converts to
another hospital type such as a CAH. We note that at this time, there
is only one urban CBSA with no IPPS hospitals; however, there are also
no IPFs located in this CBSA.
Lastly, as discussed in the FY 2024 IPPS proposed rule (88 FR
26966) in constructing the proposed FY 2024 wage index, wage data was
included for facilities that were IPPS hospitals in FY 2020, inclusive
of those facilities that have since terminated their participation in
the program as hospitals, as long as those data did not fail any of our
edits for reasonableness. We believe that including the wage data for
these hospitals is, in general, appropriate to reflect the economic
conditions in the various labor market areas during the relevant past
period and to ensure that the current wage index represents the labor
market area's current wages as compared to the national average of
wages.
Final Decision: After consideration of the comments received, we
are finalizing our proposal for FY 2024 to continue to use the
concurrent pre-floor, pre-reclassified IPPS hospital wage index as the
basis for the IPF wage index.
We will apply the IPF wage index adjustment to the labor-related
share of the national base rate and ECT payment per treatment. The
labor-related share of the national rate and ECT payment per treatment
will change from 77.4 percent in FY 2023 to 78.7 percent in FY 2024.
This percentage reflects the labor-related share of the 2021-based IPF
market basket for FY 2024 (see section IV.A.5 of this final rule).
b. Office of Management and Budget (OMB) Bulletins
i. Background
The wage index used for the IPF PPS is calculated using the
unadjusted, pre-reclassified and pre-floor IPPS wage index data and is
assigned to the IPF on the basis of the labor market area in which the
IPF is geographically located. IPF labor market areas are delineated
based on the CBSAs established by the OMB.
Generally, OMB issues major revisions to statistical areas every 10
years, based on the results of the decennial census. However, OMB
occasionally issues minor updates and revisions to statistical areas in
the years
[[Page 51087]]
between the decennial censuses through OMB Bulletins. These bulletins
contain information regarding CBSA changes, including changes to CBSA
numbers and titles. OMB bulletins may be accessed online at https://www.whitehouse.gov/wp-content/uploads/2020/03/Bulletin-20-01.pdf. In
accordance with our established methodology, the IPF PPS has
historically adopted any CBSA changes that are published in the OMB
bulletin that corresponds with the IPPS hospital wage index used to
determine the IPF wage index and, when necessary and appropriate, has
proposed and finalized transition policies for these changes.
In the RY 2007 IPF PPS final rule (71 FR 27061 through 27067), we
adopted the changes discussed in the OMB Bulletin No. 03-04 (June 6,
2003), which announced revised definitions for Micropolitan Statistical
Areas and the creation of Micropolitan Statistical Areas and Combined
Statistical Areas. In adopting the OMB CBSA geographic designations in
RY 2007, we did not provide a separate transition for the CBSA-based
wage index since the IPF PPS was already in a transition period from
TEFRA payments to PPS payments.
In the RY 2009 IPF PPS notice, we incorporated the CBSA
nomenclature changes published in the most recent OMB bulletin that
applied to the IPPS hospital wage index used to determine the current
IPF wage index and stated that we expected to continue to do the same
for all the OMB CBSA nomenclature changes in future IPF PPS rules and
notices, as necessary (73 FR 25721).
Subsequently, CMS adopted the changes that were published in past
OMB bulletins in the FY 2016 IPF PPS final rule (80 FR 46682 through
46689), the FY 2018 IPF PPS rate update (82 FR 36778 through 36779),
the FY 2020 IPF PPS final rule (84 FR 38453 through 38454), and the FY
2021 IPF PPS final rule (85 FR 47051 through 47059). We direct readers
to each of these rules for more information about the changes that were
adopted and any associated transition policies.
In part due to the scope of changes involved in adopting the CBSA
delineations for FY 2021, we finalized a 2-year transition policy
consistent with our past practice of using transition policies to help
mitigate negative impacts on hospitals of certain wage index policy
changes. We applied a 5-percent cap on wage index decreases to all IPF
providers that had any decrease in their wage indexes, regardless of
the circumstance causing the decline, so that an IPF's final wage index
for FY 2021 will not be less than 95 percent of its final wage index
for FY 2020, regardless of whether the IPF was part of an updated CBSA.
We refer readers to the FY 2021 IPF PPS final rule (85 FR 47058 through
47059) for a more detailed discussion about the wage index transition
policy for FY 2021.
On March 6, 2020 OMB issued OMB Bulletin 20-01 (available on the
web at https://www.whitehouse.gov/wp-content/uploads/2020/03/Bulletin-20-01.pdf). In considering whether to adopt this bulletin, we analyzed
whether the changes in this bulletin would have a material impact on
the IPF PPS wage index. This bulletin creates only one Micropolitan
statistical area. As discussed in further detail in section IV.D.1.b.ii
of this final rule, since Micropolitan areas are considered rural for
the IPF PPS wage index, this bulletin has no material impact on the IPF
PPS wage index. That is, the constituent county of the new Micropolitan
area was considered rural effective as of FY 2021 and would continue to
be considered rural if we adopted OMB Bulletin 20-01. Therefore, we did
not propose to adopt OMB Bulletin 20-01 in the FY 2022 IPF PPS proposed
rule.
In the FY 2023 IPF PPS final rule (87 FR 46856 through 46859), we
finalized a permanent 5-percent cap on any decrease to a provider's
wage index from its wage index in the prior year, and we stated that we
would apply this cap in a budget-neutral manner. Additionally, we
finalized a policy that a new IPF would be paid the wage index for the
area in which it is geographically located for its first full or
partial FY with no cap applied because a new IPF would not have a wage
index in the prior FY. We amended the IPF PPS regulations at Sec.
412.424(d)(1)(i) to reflect this permanent cap on wage index decreases.
We refer readers to the FY 2023 IPF PPS final rule for a more detailed
discussion about this policy.
ii. Micropolitan Statistical Areas (MSA)
OMB defines a ``Micropolitan Statistical Area'' as a CBSA
associated with at least one urban cluster that has a population of at
least 10,000, but less than 50,000 (75 FR 37252). We refer to these as
Micropolitan Areas. After extensive impact analysis, consistent with
the treatment of these areas under the IPPS as discussed in the FY 2005
IPPS final rule (69 FR 49029 through 49032), we determined the best
course of action would be to treat Micropolitan Areas as ``rural'' and
include them in the calculation of each state's IPF PPS rural wage
index. We refer the reader to the FY 2007 IPF PPS final rule (71 FR
27064 through 27065) for a complete discussion regarding treating
Micropolitan Areas as rural.
c. Adjustment for Rural Location
In the November 2004 IPF PPS final rule, (69 FR 66954), we provided
a 17 percent payment adjustment for IPFs located in a rural area. This
adjustment was based on the regression analysis, which indicated that
the per diem cost of rural facilities was 17 percent higher than that
of urban facilities after accounting for the influence of the other
variables included in the regression. This 17 percent adjustment has
been part of the IPF PPS each year since the inception of the IPF PPS.
For FY 2024, we proposed to apply a 17 percent payment adjustment for
IPFs located in a rural area as defined at Sec. 412.64(b)(1)(ii)(C)
(see 69 FR 66954 for a complete discussion of the adjustment for rural
locations).
d. Budget Neutrality Adjustment
Changes to the wage index are made in a budget-neutral manner so
that updates do not increase expenditures. Therefore, for FY 2024, we
proposed to apply a budget-neutrality adjustment in accordance with our
existing budget-neutrality policy. This policy requires us to update
the wage index in such a way that total estimated payments to IPFs for
FY 2024 are the same with or without the changes (that is, in a budget-
neutral manner) by applying a budget-neutrality factor to the IPF PPS
rates. We use the following steps to ensure that the rates reflect the
FY 2024 update to the wage indexes (based on the FY 2020 hospital cost
report data) and the labor-related share in a budget-neutral manner:
Step 1: Simulate estimated IPF PPS payments, using the FY 2023 IPF
wage index values (available on the CMS website) and labor-related
share (as published in the FY 2023 IPF PPS final rule (87 FR 46846).
Step 2: Simulate estimated IPF PPS payments using the FY 2024 IPF
wage index values (available on the CMS website) and FY 2024 labor-
related share (based on the latest available data as discussed
previously).
Step 3: Divide the amount calculated in step 1 by the amount
calculated in step 2. The resulting quotient is the FY 2024 budget-
neutral wage adjustment factor of 1.0016.
Step 4: Apply the FY 2024 budget-neutral wage adjustment factor
from step 3 to the FY 2023 IPF PPS Federal per diem base rate after the
application of the market basket update described in section IV.A of
this final rule, to determine the FY 2024 IPF PPS Federal per diem base
rate.
[[Page 51088]]
2. Teaching Adjustment
a. Background
In the November 2004 IPF PPS final rule, we implemented regulations
at Sec. 412.424(d)(1)(iii) to establish a facility-level adjustment
for IPFs that are, or are part of, teaching hospitals. The teaching
adjustment accounts for the higher indirect operating costs experienced
by hospitals that participate in graduate medical education (GME)
programs. The payment adjustments are made based on the ratio of the
number of fulltime equivalent (FTE) interns and residents training in
the IPF and the IPF's average daily census.
Medicare makes direct GME payments (for direct costs such as
resident and teaching physician salaries, and other direct teaching
costs) to all teaching hospitals including those paid under a PPS, and
those paid under the TEFRA rate-of-increase limits. These direct GME
payments are made separately from payments for hospital operating costs
and are not part of the IPF PPS. The direct GME payments do not address
the estimated higher indirect operating costs teaching hospitals may
face.
The results of the regression analysis of FY 2002 IPF data
established the basis for the payment adjustments included in the
November 2004 IPF PPS final rule. The results showed that the indirect
teaching cost variable is significant in explaining the higher costs of
IPFs that have teaching programs. We calculated the teaching adjustment
based on the IPF's ``teaching variable'', which is (1 + [the number of
FTE residents training in the IPF's average daily census]). The
teaching variable is then raised to the 0.5150 power to result in the
teaching adjustment. This formula is subject to the limitations on the
number of FTE residents, which are described in this section of this
final rule.
We established the teaching adjustment in a manner that limited the
incentives for IPFs to add FTE residents for the purpose of increasing
their teaching adjustment. We imposed a cap on the number of FTE
residents that may be counted for purposes of calculating the teaching
adjustment. The cap limits the number of FTE residents that teaching
IPFs may count for the purpose of calculating the IPF PPS teaching
adjustment, not the number of residents teaching institutions can hire
or train. We calculated the number of FTE residents that trained in the
IPF during a ``base year'' and used that FTE resident number as the
cap. An IPF's FTE resident cap is ultimately determined based on the
final settlement of the IPF's most recent cost report filed before
November 15, 2004 (69 FR 66955). A complete discussion of the temporary
adjustment to the FTE cap to reflect residents due to hospital closure
or residency program closure appears in the RY 2012 IPF PPS proposed
rule (76 FR 5018 through 5020) and the RY 2012 IPF PPS final rule (76
FR 26453 through 26456).
In the regression analysis, the logarithm of the teaching variable
had a coefficient value of 0.5150. We converted this cost effect to a
teaching payment adjustment by treating the regression coefficient as
an exponent and raising the teaching variable to a power equal to the
coefficient value. We note that the coefficient value of 0.5150 was
based on the regression analysis holding all other components of the
payment system constant. A complete discussion of how the teaching
adjustment was calculated appears in the November 2004 IPF PPS final
rule (69 FR 66954 through 66957) and the RY 2009 IPF PPS notice (73 FR
25721). As with other adjustment factors derived through the regression
analysis, we do not plan to propose updates to the teaching adjustment
factors until we more fully analyze IPF PPS data. Therefore, in this FY
2024 final rule, we are retaining the coefficient value of 0.5150 for
the teaching adjustment to the Federal per diem base rate.
Comment: One commenter recommended CMS update its methodology for
calculating the IPF teaching adjustment, particularly in recognition of
the Congress authorizing the awarding of new Medicare-reimbursable
residency positions under the CAA, 2023 and the Consolidated
Appropriations Act, 2021 (hereafter referred to as CAA, 2021) (Pub. L.
116-260). This commenter suggested CMS collect information on awards of
new Medicare residency positions under section 126 of division CC, CAA,
2021 and section 4122 of CAA, 2023 from those hospitals subject to the
IPF so that it can provide resident FTE cap increases under the IPF for
those hospitals that receive awards for psychiatry programs.
One commenter requested that CMS permit IPFs to aggregate and
adjust their FTE caps through affiliation agreements. The commenter
noted training residents often indirectly increases the hospital's
operational costs, but freestanding IPFs that take over this role are
unable to receive any corresponding payment increase that was
previously available to the host-hospital distinct part unit (DPU).
Response: We appreciate the commenter's suggestion regarding
potential changes to the IPF teaching adjustment to recognize new
Medicare-reimbursable residency positions under the CAA, 2023 and the
CAA, 2021. The CAA, 2021 and CAA, 2023 established resident slots for
direct medical education and indirect medical education, which are paid
under the IPPS. We will take this comment into consideration to
potentially inform future rulemaking for the IPF PPS.
Regarding the commenter's suggestion to recognize affiliation
agreements, we did not propose to recognize affiliation agreements for
the IPF PPS teaching adjustment and are not making a change to this
policy. As we previously stated in the RY 2005 IPF PPS final rule (69
FR 66956), our intent is not to affect affiliation agreements and
rotational arrangements for hospitals that have residents that train in
more than one hospital. We have not implemented a provision concerning
affiliation agreements specifically pertaining to the FTE caps used in
the teaching adjustment under the IPF PPS.
Final Decision: We are finalizing as proposed to calculate the IPF
teaching adjustment according to our established methodology.
3. Cost of Living Adjustment (COLA) for IPFs Located in Alaska and
Hawaii
The IPF PPS includes a payment adjustment for IPFs located in
Alaska and Hawaii based upon the area in which the IPF is located. As
we explained in the November 2004 IPF PPS final rule, the FY 2002 data
demonstrated that IPFs in Alaska and Hawaii had per diem costs that
were disproportionately higher than other IPFs. Other Medicare
prospective payment systems (for example, the IPPS and LTCH PPS)
adopted a COLA to account for the cost differential of care furnished
in Alaska and Hawaii.
We analyzed the effect of applying a COLA to payments for IPFs
located in Alaska and Hawaii. The results of our analysis demonstrated
that a COLA for IPFs located in Alaska and Hawaii will improve payment
equity for these facilities. As a result of this analysis, we provided
a COLA in the November 2004 IPF PPS final rule.
A COLA for IPFs located in Alaska and Hawaii is made by multiplying
the non-labor-related portion of the Federal per diem base rate by the
applicable COLA factor based on the COLA area in which the IPF is
located.
The COLA factors through 2009 were published by the Office of
Personnel Management (OPM), and the OPM memo showing the 2009 COLA
factors is available at https://www.chcoc.gov/
[[Page 51089]]
content/nonforeign-area-retirement-equity-assurance-act.
We note that the COLA areas for Alaska are not defined by county as
are the COLA areas for Hawaii. In 5 CFR 591.207, the OPM established
the following COLA areas:
City of Anchorage, and 80-kilometer (50-mile) radius by
road, as measured from the Federal courthouse.
City of Fairbanks, and 80-kilometer (50-mile) radius by
road, as measured from the Federal courthouse.
City of Juneau, and 80-kilometer (50-mile) radius by road,
as measured from the Federal courthouse.
Rest of the state of Alaska.
As stated in the November 2004 IPF PPS final rule, we update the
COLA factors according to updates established by the OPM. However,
sections 1911 through 1919 of the Non-foreign Area Retirement Equity
Assurance Act, as contained in subtitle B of title XIX of the National
Defense Authorization Act (NDAA) (Pub. L. 111-84, October 28, 2009),
for FY 2010 transitions the Alaska and Hawaii COLAs to locality pay.
Under section 1914 of NDAA, locality pay was phased in over a 3-year
period beginning in January 2010, with COLA rates frozen as of the date
of enactment, October 28, 2009, and then proportionately reduced to
reflect the phase-in of locality pay.
When we published the proposed COLA factors in the RY 2012 IPF PPS
proposed rule (76 FR 4998), we inadvertently selected the FY 2010 COLA
rates, which had been reduced to account for the phase-in of locality
pay. We did not intend to propose the reduced COLA rates because that
would have understated the adjustment. Since the 2009 COLA rates did
not reflect the phase-in of locality pay, we finalized the FY 2009 COLA
rates for RY 2010 through RY 2014.
In the FY 2013 IPPS/LTCH final rule (77 FR 53700 through 53701), we
established a new methodology to update the COLA factors for Alaska and
Hawaii and adopted this methodology for the IPF PPS in the FY 2015 IPF
PPS final rule (79 FR 45958 through 45960). We adopted this new COLA
methodology for the IPF PPS because IPFs are hospitals with a similar
mix of commodities and services. We believe it is appropriate to have a
consistent policy approach with that of other hospitals in Alaska and
Hawaii. Therefore, the IPF COLAs for FY 2015 through FY 2017 were the
same as those applied under the IPPS in those years. As finalized in
the FY 2013 IPPS/LTCH PPS final rule (77 FR 53700 and 53701), the COLA
updates are determined every 4 years, when the IPPS market basket
labor-related share is updated. Because the labor-related share of the
IPPS market basket was updated for FY 2022, the COLA factors were
updated in FY 2022 IPPS/LTCH rulemaking (86 FR 45547). As such, we also
updated the IPF PPS COLA factors for FY 2022 (86 FR 42621 through
42622) to reflect the updated COLA factors finalized in the FY 2022
IPPS/LTCH rulemaking. Table 16 shows the IPF PPS COLA factors effective
for FY 2022 through FY 2025.
[GRAPHIC] [TIFF OMITTED] TR02AU23.017
The IPF PPS COLA factors for FY 2024 are also shown in Addendum A
to this final rule, which is available at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/InpatientPsychFacilPPS/tools.html.
4. Adjustment for IPFs With a Qualifying Emergency Department (ED)
The IPF PPS includes a facility-level adjustment for IPFs with
qualifying EDs. We provide an adjustment to the Federal per diem base
rate to account for the costs associated with maintaining a full-
service ED. The adjustment is intended to account for ED costs incurred
by a psychiatric hospital with a qualifying ED or an excluded
psychiatric unit of an IPPS hospital or a CAH, for preadmission
services otherwise payable under the Medicare Hospital Outpatient
Prospective Payment System (OPPS), furnished to a beneficiary on the
date of the beneficiary's admission to the hospital and during the day
immediately preceding the date of admission to the IPF (see Sec.
413.40(c)(2)), and the overhead cost of maintaining the ED. This
payment is a facility-level adjustment that applies to all IPF
admissions (with one exception, which we described), regardless of
whether a particular patient receives preadmission services in the
hospital's ED.
The ED adjustment is incorporated into the variable per diem
adjustment for the first day of each stay for IPFs with a qualifying
ED. Those IPFs with a qualifying ED receive an adjustment factor of
1.31 as the variable per diem adjustment for day 1 of each patient
stay. If an IPF does not have a qualifying ED, it receives an
adjustment factor of 1.19 as the variable per diem adjustment for day 1
of each patient stay.
The ED adjustment is made on every qualifying claim except as
described in
[[Page 51090]]
this section of this final rule. As specified in Sec.
412.424(d)(1)(v)(B), the ED adjustment is not made when a patient is
discharged from an IPPS hospital or CAH and admitted to the same IPPS
hospital's or CAH's excluded psychiatric unit. We clarified in the
November 2004 IPF PPS final rule (69 FR 66960) that an ED adjustment is
not made in this case because the costs associated with ED services are
reflected in the DRG payment to the IPPS hospital or through the
reasonable cost payment made to the CAH.
Therefore, when patients are discharged from an IPPS hospital or
CAH and admitted to the same hospital's or CAH's excluded psychiatric
unit, the IPF receives the 1.19 adjustment factor as the variable per
diem adjustment for the first day of the patient's stay in the IPF. For
FY 2024, we proposed to retain the 1.31 adjustment factor for IPFs with
qualifying EDs. A complete discussion of the steps involved in the
calculation of the ED adjustment factors are in the November 2004 IPF
PPS final rule (69 FR 66959 through 66960) and the RY 2007 IPF PPS
final rule (71 FR 27070 through 27072).
As we did not propose any changes to the ED adjustment, we are
retaining the existing ED adjustment for FY 2024.
E. Other Proposed Payment Adjustments and Policies
1. Outlier Payment Overview
The IPF PPS includes an outlier adjustment to promote access to IPF
care for those patients who require expensive care and to limit the
financial risk of IPFs treating unusually costly patients. In the
November 2004 IPF PPS final rule, we implemented regulations at Sec.
412.424(d)(3)(i) to provide a per case payment for IPF stays that are
extraordinarily costly. Providing additional payments to IPFs for
extremely costly cases strongly improves the accuracy of the IPF PPS in
determining resource costs at the patient and facility level. These
additional payments reduce the financial losses that would otherwise be
incurred in treating patients who require costlier care, and therefore,
reduce the incentives for IPFs to under-serve these patients. We make
outlier payments for discharges in which an IPF's estimated total cost
for a case exceeds a fixed dollar loss threshold amount (multiplied by
the IPF's facility-level adjustments) plus the Federal per diem payment
amount for the case.
In instances when the case qualifies for an outlier payment, we pay
80 percent of the difference between the estimated cost for the case
and the adjusted threshold amount for days 1 through 9 of the stay
(consistent with the median LOS for IPFs in FY 2002), and 60 percent of
the difference for day 10 and thereafter. The adjusted threshold amount
is equal to the outlier threshold amount adjusted for wage area,
teaching status, rural area, and the COLA adjustment (if applicable),
plus the amount of the Medicare IPF payment for the case. We
established the 80 percent and 60 percent loss sharing ratios because
we were concerned that a single ratio established at 80 percent (like
other Medicare PPSs) might provide an incentive under the IPF per diem
payment system to increase LOS in order to receive additional payments.
After establishing the loss sharing ratios, we determined the
current fixed dollar loss threshold amount through payment simulations
designed to compute a dollar loss beyond which payments are estimated
to meet the 2 percent outlier spending target. Each year when we update
the IPF PPS, we simulate payments using the latest available data to
compute the fixed dollar loss threshold so that outlier payments
represent 2 percent of total estimated IPF PPS payments.
2. Update to the Outlier Fixed Dollar Loss Threshold Amount
In accordance with the update methodology described in Sec.
412.428(d), we proposed to update the fixed dollar loss threshold
amount used under the IPF PPS outlier policy. Based on the regression
analysis and payment simulations used to develop the IPF PPS, we
established a 2 percent outlier policy, which strikes an appropriate
balance between protecting IPFs from extraordinarily costly cases while
ensuring the adequacy of the Federal per diem base rate for all other
cases that are not outlier cases.
Our longstanding methodology for updating the outlier fixed dollar
loss threshold involves using the best available data, which is
typically the most recent available data. For the FY 2022 IPF PPS final
rule, we finalized the use of FY 2019 claims rather than the more
recent FY 2020 claims for updating the outlier fixed dollar loss
threshold (86 FR 42623). We noted that our use of the FY 2019 claims to
set the final outlier fixed dollar loss threshold for FY 2022 deviated
from our longstanding practice of using the most recent available year
of claims but remained otherwise consistent with the established
outlier update methodology. We explained that we finalized our proposal
to deviate from our longstanding practice of using the most recent
available year of claims only because, and to the extent that, the
``coronavirus disease 2019'' (abbreviated ``COVID-19'') Public Health
Emergency (PHE) appeared to have significantly impacted the FY 2020 IPF
claims. We further stated that we intended to continue to analyze
further data in order to better understand both the short-term and
long-term effects of the COVID-19 PHE on IPFs (86 FR 42624).
In the FY 2023 IPF PPS final rule (87 FR 46862 through 46864) we
noted that we observed an overall increase in average cost per day and
an overall decrease in the number of covered days. However, we
identified that some providers had significant increases in their
charges, resulting in higher-than-normal estimated cost per day that
would skew our estimate of outlier payments for FY 2022 and FY 2023. We
finalized our proposal for FY 2023 to use the latest available FY 2021
claims, in accordance with our longstanding practice, to simulate
payments for determining the final FY 2023 IPF PPS outlier fixed dollar
loss threshold amount. In addition, we finalized a methodology for FY
2023 to exclude providers from our impact simulations whose change in
simulated cost per day is outside 3 standard deviations from the mean.
For the FY 2024 IPF PPS proposed rule, consistent with our
longstanding practice, we analyzed the most recent available data for
simulating IPF PPS payments in FY 2023. Based on an analysis of these
updated data, we estimated that IPF outlier payments as a percentage of
total estimated payments were approximately 3.0 percent in FY 2023. We
analyzed the change in providers' charges from the FY 2021 claims that
were used to simulate payments for determining the final FY 2023 IPF
PPS outlier threshold, and the latest available FY 2022 claims. In
contrast to our analysis of FY 2021 claims for the FY 2023 IPF PPS
proposed and final rules, we did not find the same level of significant
increases in charges in the FY 2022 claims that we believe would skew
our estimate of outlier payments for FY 2023 and FY 2024. Therefore, we
proposed to update the outlier threshold amount to $34,750. This would
allow us to maintain estimated outlier payments at 2 percent of total
estimated aggregate IPF payments for FY 2024. This proposed update was
an increase from the FY 2023 threshold of $24,630. We solicited
comments on this proposed increase to the outlier threshold for FY
2024, and whether we should consider alternative methodologies for FY
2024.
[[Page 51091]]
Specifically, we were interested in understanding whether commenters
believe it would be appropriate to exclude providers from our FY 2024
impact simulations whose change in simulated cost per day is outside 3
standard deviations from the mean, following the same methodology we
applied in FY 2023. We noted that our analysis for the FY 2024 proposed
rule showed that the FY 2024 outlier fixed dollar loss threshold amount
would be closer to $30,000 if we were to exclude providers based on the
same methodology finalized for FY 2023. We were also interested in
other methodologies that commenters believe might be appropriate to
consider, including why commenters believe applying such a methodology
would be appropriate for establishing the outlier threshold for FY
2024.
Comment: We received five comments in response to the FY 2024 IPF
PPS pertaining to an alternative IPF PPS outlier policy. Commenters
included state-level and national provider associations. One commenter
stated the increase in the outlier threshold amount should be limited
to no more than the market basket update for the year but did not
provide a rationale for this suggestion. Two commenters recommended CMS
mitigate the financial impact that imperfect outlier threshold
estimates have on IPFs. Four commenters requested that CMS explain in
greater detail the factors driving the increase and that CMS examine
its methodology and consider making changes to mitigate increases to
the outlier threshold. Commenters also requested information on how the
proposed increase would affect the IPF field and its patients.
Response: We appreciate the suggestions from commenters regarding
mitigating the financial impact of the outlier threshold on IPFs and
the use of alternative methodologies for estimating the outlier
threshold. We are not finalizing any of the alternative methodologies
that commenters suggested, but we are providing additional information
about the drivers and impact of the increase to the outlier threshold,
as commenters requested.
As we previously noted in the FY 2023 final rule (87 FR 46863), we
observed two main trends in the claims data for FY 2020 and FY 2021. In
summary, these were an increase in average cost per day and a decrease
in total IPF PPS payments corresponding with a decrease in covered IPF
PPS days. Both of these trends continued in the FY 2022 claims data
used for this FY 2024 IPF PPS final rule. First, we observed that
average cost per day increased approximately 8 percent when comparing
the simulated FY 2022 IPF PPS payments from the FY 2023 IPF PPS final
rule to the simulated FY 2023 IPF PPS payments that we used to estimate
the outlier percentage for this FY 2024 IPF PPS final rule. In the FY
2022 IPF PPS proposed rule (86 FR 19526), we explained that we estimate
the costs per case based on the covered charges on each IPF claim and
the IPF's most recent CCR. The second continued trend that we observed
was that the number of covered days continued to decrease in the FY
2022 claims. The number of covered days in the FY 2022 claims were
approximately 12 percent lower than the number of covered days in the
FY 2021 claims used for FY 2023 final rulemaking, before applying the
statistical trim for the FY 2023 IPF PPS final rule (87 FR 46862). This
decrease in covered days corresponds with a decrease of approximately
10 percent in the total simulated FY 2023 IPF PPS payments compared to
total simulated FY 2022 IPF PPS payments used for FY 2023 final
rulemaking. In addition, when comparing the data used for this FY 2024
IPF PPS final rule with the statistically trimmed data used for the FY
2023 IPF PPS final rule, the covered days for FY 2024 were
approximately 8 percent lower than FY 2023, and total simulated FY 2023
IPF PPS payments that we used to estimate the outlier percentage for
this FY 2024 IPF PPS final rule were approximately 4 percent lower than
total simulated FY 2022 IPF PPS payments. Because we calculate the
outlier fixed dollar loss threshold amount so that outlier payments
represent 2 percent of total estimated IPF PPS payments, the decrease
to the number of days and total estimated IPF PPS payments increases
the percentage of outlier payments relative to total payments, which
contributes to the upward trend in the outlier fixed dollar loss
threshold amount. In our simulated FY 2023 outlier payments using the
FY 2023 IPF PPS outlier fixed dollar loss threshold of $24,630, we
estimated that 5,817 cases will receive outlier payments, with a mean
outlier payment amount per outlier case of $13,807.28. We observed that
the distribution of simulated FY 2023 outlier payments is skewed right,
which means that a large number of outlier cases receive relatively
small amounts of outlier payments, and a smaller number of outlier
cases receive relatively large outlier payments. Consequently, half of
all simulated outlier cases receive outlier payments of $7,543.65 or
less, and 559 cases receive outlier payments of $1,000 or less. We also
observed that outlier payments are concentrated among certain types of
IPFs. As shown in Table 40, in section VIII.C.2 of this final rule,
urban government-owned IPF units are projected to experience the
largest decreases in estimated payments as a result of the increase to
the outlier fixed dollar loss threshold amount, because these providers
had a larger share of outlier cases than other provider types. We did
not observe that changes in case mix appear to be driving the increase
in the outlier percentage. In the simulated FY 2023 IPF PPS payments,
we observed that approximately 79 percent of outlier cases are for DRG
885 (Psychoses), which aligns with the proportion of IPF PPS cases that
typically receive that DRG. We estimate that the average outlier
payment for cases with DRG 885 is $14,485.21, which is comparable to
the average outlier payment for all cases.
Regarding the suggestion to limit increases to the outlier
threshold to no more than the market basket update, we are concerned
that this methodology would not be technically appropriate for the IPF
PPS outlier policy. As discussed earlier in this section, the
longstanding IPF PPS 2-percent outlier policy was established based on
the regression analysis and payment simulations used to develop the IPF
PPS. We have previously explained that the 2-percent outlier policy
strikes an appropriate balance between protecting IPFs from
extraordinarily costly cases while ensuring the adequacy of the Federal
per diem base rate for all other cases that are not outlier cases. Each
year when we update the IPF PPS, we simulate payments using the latest
available data to compute the fixed dollar loss threshold so that
outlier payments represent 2 percent of total estimated IPF PPS
payments. For this FY 2024 IPF PPS final rule, we have simulated
payments using the latest available data, and these payment simulations
indicate that an increase to the outlier fixed dollar loss threshold is
necessary in order to maintain outlier payments at 2 percent of total
payments. We are concerned that limiting increases to the outlier fixed
dollar loss threshold to no more than the market basket update
percentage would not appropriately target outlier payments such that
they remain at 2 percent of total IPF PPS payments and that such a
policy would increase outlier payments above the 2 percent target for
FY 2024. As we noted in the prior paragraph, we observe that the
increase in the outlier fixed dollar loss threshold is driven in part
by a continual downward trend in
[[Page 51092]]
covered days over the past several years. We are concerned that it
would not be appropriate to increase outlier payments to offset the
fact that IPFs are providing fewer days of care for Medicare
beneficiaries.
Final Decision: After consideration of the comments received, we
are finalizing our proposal to update the fixed dollar loss threshold
amount used under the IPF PPS outlier policy. Based on the latest
available data, we are finalizing an outlier fixed dollar loss
threshold amount of $33,470 for FY 2024.
3. Update to IPF Cost-To-Charge Ratio Ceilings
Under the IPF PPS, an outlier payment is made if an IPF's cost for
a stay exceeds a fixed dollar loss threshold amount plus the IPF PPS
amount. In order to establish an IPF's cost for a particular case, we
multiply the IPF's reported charges on the discharge bill by its
overall cost-to-charge ratio (CCR). This approach to determining an
IPF's cost is consistent with the approach used under the IPPS and
other PPSs. In the FY 2004 IPPS final rule (68 FR 34494), we
implemented changes to the IPPS policy used to determine CCRs for IPPS
hospitals, because we became aware that payment vulnerabilities
resulted in inappropriate outlier payments. Under the IPPS, we
established a statistical measure of accuracy for CCRs to ensure that
aberrant CCR data did not result in inappropriate outlier payments.
As indicated in the November 2004 IPF PPS final rule (69 FR 66961),
we believe that the IPF outlier policy is susceptible to the same
payment vulnerabilities as the IPPS; therefore, we adopted a method to
ensure the statistical accuracy of CCRs under the IPF PPS.
Specifically, we adopted the following procedure in the November 2004
IPF PPS final rule:
Calculated two national ceilings, one for IPFs located in
rural areas and one for IPFs located in urban areas.
Computed the ceilings by first calculating the national
average and the standard deviation of the CCR for both urban and rural
IPFs using the most recent CCRs entered in the most recent Provider
Specific File (PSF) available.
For FY 2024, we proposed to continue to follow this methodology.
To determine the rural and urban ceilings, we multiplied each of
the standard deviations by 3 and added the result to the appropriate
national CCR average (either rural or urban). The upper threshold CCR
for IPFs in FY 2024 is 2.1419 for rural IPFs, and 1.8026 for urban
IPFs, based on CBSA-based geographic designations. If an IPF's CCR is
above the applicable ceiling, the ratio is considered statistically
inaccurate, and we assign the appropriate national (either rural or
urban) median CCR to the IPF.
We apply the national median CCRs to the following situations:
New IPFs that have not yet submitted their first Medicare
cost report. We continue to use these national median CCRs until the
facility's actual CCR can be computed using the first tentatively or
final settled cost report.
IPFs whose overall CCR is in excess of three standard
deviations above the corresponding national geometric mean (that is,
above the ceiling).
Other IPFs for which the Medicare Administrative
Contractor (MAC) obtains inaccurate or incomplete data with which to
calculate a CCR.
We proposed to update the FY 2024 national median and ceiling CCRs
for urban and rural IPFs based on the CCRs entered in the latest
available IPF PPS PSF.
Specifically, for FY 2024, to be used in each of the three
situations listed previously, using the most recent CCRs entered in the
CY 2022 PSF, we provided an estimated national median CCR of 0.5720 for
rural IPFs and a national median CCR of 0.4200 for urban IPFs. These
calculations are based on the IPF's location (either urban or rural)
using the CBSA-based geographic designations. A complete discussion
regarding the national median CCRs appears in the November 2004 IPF PPS
final rule (69 FR 66961 through 66964).
4. Modification to the Regulation for Excluded Psychiatric Units Paid
Under the IPF PPS
a. Background
Under current regulation, in order to be excluded from the IPPS and
paid under the IPF PPS or the IRF PPS, an IPF or IRF unit of a hospital
must meet a number of requirements under 42 CFR 412.25. As discussed in
the following paragraphs, both this regulation and the policies
applying to excluded units (which include excluded IRF units and
excluded IPF units) have been in effect since before both the IPF PPS
and IRF PPS were established. Before the IRF PPS and the IPF PPS were
established, excluded units were paid based on their costs, as reported
on their Medicare cost reports, subject to certain facility-specific
cost limits. These cost-based payments were determined separately for
operating and capital costs. Thus, under cost-based payments, the
process of allocating costs to an IPF unit for reimbursement created
significant administrative complexity. This administrative complexity
necessitated strict regulations that allowed hospitals to open a new
IPPS-excluded unit only at the start of a cost reporting period.
In the January 3, 1984 final rule (49 FR 235), CMS (then known as
the Health Care Financing Administration) established policies and
regulations for hospitals and units subject to and excluded from the
IPPS. In that rule, we explained that section 1886(d) of the Act
requires that the prospective payment system apply to inpatient
hospital services furnished by all hospitals participating in the
Medicare program except those hospitals or units specifically excluded
by the law. We further explained our expectation that a hospital's
status (that is, whether it is subject to, or excluded from, the
prospective payment system) would generally be determined at the
beginning of each cost reporting period. We also stated that this
status would continue throughout the period, which is normally 1 year.
Accordingly, we stated that changes in a hospital's (or unit's) status
that result from meeting or failing to meet the criteria for exclusion
would be implemented only at the start of a cost reporting period.
However, we also acknowledged that under some circumstances involving
factors external to the hospital, status changes could be made at times
other than the beginning of the cost reporting period. For example, a
change in status could occur if a hospital is first included under the
prospective payment system and, after the start of its cost reporting
period, is excluded because of its participation in an approved
demonstration project or State reimbursement control program that
begins after the hospital's cost reporting period has begun.
In the 1993 IPPS final rule (57 FR 39798 through 39799), we
codified our longstanding policies regarding when a hospital unit can
change its status from not excluded to excluded. We explained in that
final rule that since the inception of the PPS for operating costs of
hospital inpatient services in October 1983, certain types of
specialty-care hospitals and hospital units have been excluded from
that system under section 1888(d)(1)(B) of the Act. We noted that these
currently include psychiatric and rehabilitation hospitals and distinct
part units, children's hospitals, and long-term care hospitals. We
further explained that section 6004(a)(1) of Public Law 101-239 amended
section 1886(d)(1)(B) of the Act to provide that certain cancer
hospitals are also excluded. We noted that the preamble to the January
3, 1984 final rule
[[Page 51093]]
implementing the PPS for operating costs (49 FR 235) stated that the
status of a hospital or unit (that is, whether it is subject to, or
excluded from, the PPS) will be determined at the beginning of each
cost reporting period. We noted that that same 1984 final rule also
provided that changes in a hospital's or unit's status that result from
meeting or failing to meet the criteria for exclusion will be
implemented prospectively only at the start of a cost reporting period,
that is, starting with the beginning date of the next cost reporting
period (49 FR 243). However, we noted that this policy was not set
forth in the regulations. In that 1993 IPPS final rule, we stated that
we proposed revising Sec. Sec. 412.22 and 412.25 to specify that
changes in the status of each hospital or hospital unit would be
recognized only at the start of a cost reporting period. We stated
that, except in the case of retroactive payment adjustments for
excluded rehabilitation units described in Sec. 412.30(c), any change
in a hospital's or unit's compliance with the exclusion criteria that
occurs after the start of a cost reporting period would not be taken
into consideration until the start of the following period. We noted
that this policy would also apply to any unit that is added to a
hospital during the hospital's cost reporting period. We also stated
that we proposed revising Sec. 412.25(a) to specify that as a
requirement for exclusion, a hospital unit must be fully equipped and
staffed, and be capable of providing inpatient psychiatric or
rehabilitation care as of the first day of the first cost reporting
period for which all other exclusion requirements are met. We explained
that a unit that meets this requirement would be considered open
regardless of whether there are any inpatients in the unit.
In the same 1993 IPPS final rule, we responded to commenters who
objected to this policy, stating that it unnecessarily penalizes
hospitals for factors beyond their control, such as construction
delays, that it discourages hospitals from making changes in their
programs to meet community needs, or that it can place undue workload
demands on regulatory agencies during certain time periods. In
response, we explained that we believed that regulatory agencies,
hospitals, and the public generally would benefit from policies that
are clearly stated, can be easily understood by both hospitals and
intermediaries, and can be simply administered. We stated that
recognizing changes in status only at the beginning of cost reporting
periods is consistent with these goals, while recognizing changes in
the middle of cost reporting periods would introduce added complexity
to the administration of the exclusion provisions. Therefore, we did
not revise the proposed changes based on these comments.
In the FY 2000 IPPS final rule (64 FR 41531 through 41532), we
amended the regulations at Sec. 412.25(c) to allow a hospital unit to
change from excluded to not excluded at any time during the cost
reporting period. We explained the statutory basis and rationale for
this change in the FY 2000 IPPS proposed rule (64 FR 24740) and noted
that a number of hospitals suggested that we consider a change in our
policy to recognize, for purposes of exclusion from the IPPS,
reductions in number of beds in, or entire closure of, units at any
time during a cost reporting period. In that FY 2000 IPPS proposed
rule, we explained that hospitals indicated that the bed capacity made
available as a result of these changes could be used as needed to
provide additional services to meet patient needs in the acute care
part of the hospital that is paid under the IPPS. We further explained
that we evaluated the concerns of the hospitals and the effects on the
administration of the Medicare program and the health care of
beneficiaries of making these payment changes. As a result of that
evaluation, we stated that we believed it was reasonable to adopt a
more flexible policy in recognition of hospitals' changes in the use of
their facilities. However, we noted that whenever a hospital
establishes an excluded unit within the hospital, our Medicare fiscal
intermediary would need to be able to determine costs of the unit
separately from costs of the part of the hospital paid under the
prospective payment system. At that time, we stated that the proper
determination of costs ensured that the hospital was paid the correct
amount for services in each part of the facility, and that payments
under the IPPS did not duplicate payments made under the rules that
were applicable to excluded hospitals and units, or vice versa. For
this reason, we did not believe it would be appropriate to recognize,
for purposes of exclusion from the IPPS, changes in the bed size or
status of an excluded unit that are so frequent that they interfere
with the ability of the intermediary to accurately determine costs.
Moreover, we explained that section 1886(d)(1)(B) of the Act authorizes
exclusion from the IPPS of specific types of hospitals and units, but
not of specific admissions or stays, such as admissions for
rehabilitation or psychiatric care, in a hospital paid under the IPPS.
We stated that without limits on the frequency of changes in excluded
units for purposes of proper Medicare payment, there was the potential
for some hospitals to adjust the status or size of their excluded units
so frequently that the units would no longer be distinct entities and
the exclusion would effectively apply only to certain types of care.
In the FY 2012 IRF PPS final rule (76 FR 47870), we began further
efforts to increase flexibilities for excluded IPF and IRF units. In
that rule, we explained that cost-based reimbursement methodologies
that were in place before the IPF PPS and IRF PPS meant that the
facilities' capital costs were determined, in part, by their bed size
and square footage. Changes in the bed size and square footage would
complicate the facilities' capital cost allocation. Thus, regulations
at Sec. 412.25 limited the situations under which an IRF or IPF could
change its bed size and square footage. In the FY 2012 IRF PPS final
rule, we revised Sec. 412.25(b) to enable IRFs and IPFs to more easily
adjust to beneficiary changes in demand for IRF or IPF services and
improve beneficiary access to these services. We believed that the
first requirement (that beds can only be added at the start of a cost
reporting period) was difficult, and potentially costly, for IRFs and
IPFs that were expanding through new construction because the exact
timing of the end of a construction project is often difficult to
predict. In that same FY 2012 IRF PPS final rule, commenters suggested
that CMS allow new IRF units or new IPF units to open and begin being
paid under their respective IRF PPS or IPF PPS at any time during a
cost reporting period, rather than requiring that they could only begin
being paid under the IRF PPS or the IPF PPS at the start of a cost
reporting period. We believed that this suggestion was outside the
scope of the FY 2012 IRF PPS proposed rule (76 FR 24214), because we
did not propose any changes to the Sec. 412.25(c). However, we stated
that we would consider this suggestion for possible inclusion in future
rulemaking.
b. Current Challenges Related to Excluded Hospital Units (Sec. Sec.
412.25(c)(1) and (c)(2))
Currently, under Sec. 412.25(c)(1), a hospital can only start
being paid under the IPF PPS or the IRF PPS for services provided in an
excluded hospital unit at the start of a cost reporting period.
Specifically, Sec. 412.25(c) limits when the status of hospital units
may change for purposes of exclusion from the IPPS, as specified in
Sec. Sec. 412.25(c)(1) and
[[Page 51094]]
412.25(c)(2). Section 412.25(c)(1) states that the status of a hospital
unit may be changed from not excluded to excluded only at the start of
the cost reporting period. If a unit is added to a hospital after the
start of a cost reporting period, it cannot be excluded from the IPPS
before the start of a hospital's next cost reporting period. Section
412.25(c)(2) states the status of a hospital unit may be changed from
excluded to not excluded at any time during a cost reporting period,
but only if the hospital notifies the fiscal intermediary and the CMS
Regional Office in writing of the change at least 30 days before the
date of the change, and maintains the information needed to accurately
determine costs that are or are not attributable to the excluded unit.
A change in the status of a unit from excluded to not excluded that is
made during a cost reporting period must remain in effect for the rest
of that cost reporting period.
In recent years, interested parties, such as hospitals, have
written CMS to express concerns about what they see as the unnecessary
restrictiveness of the requirements at Sec. 412.25(c). Based on this
feedback, we continued to explore opportunities to reduce burden for
providers and clinicians, while keeping patient-centered care a
priority. For instance, we considered whether this regulation might
create unnecessary burden for hospitals and potentially delay necessary
psychiatric beds from opening and being paid under the IPF PPS. As we
continued to review and reconsider regulations to identify ways to
improve policy, we recognized that the requirement at Sec.
412.25(c)(1), that hospital units can only be excluded at the start of
a cost reporting period, may be challenging and potentially costly for
facilities under some circumstances, for example, those that are
expanding through new construction. Hospitals have indicated it is
often difficult to predict the exact timing of the end of a
construction project and construction delays may hamper a hospital's
ability to have the construction of an excluded unit completed exactly
at the start of a cost reporting period, which hospitals have said can
lead to significant revenue loss if they are unable to be paid under
the IPF PPS or IRF PPS until the start of the next cost reporting
period.
As previously stated, the requirements at Sec. 412.25(c) were
established to manage the administrative complexity associated with
cost-based reimbursement for excluded IPF and IRF units. Today,
however, because IPF units are paid under the IPF PPS and IRF units are
paid under the IRF PPS, cost allocation is not used for payment
purposes. Because advancements in technology since the inception of the
IPF PPS and IRF PPS have simplified the cost reporting process and
enhanced communication between providers, Medicare contractors, and
CMS, we are reconsidering whether it is necessary to continue to allow
hospital units to become excluded only at the start of a cost reporting
period.
c. Changes to Excluded Hospital Units (Sec. Sec. 412.25(c)(1) and
(c)(2))
We are committed to continuing to transform the health care
delivery system and the Medicare program by putting additional focus on
patient-centered care and working with providers, physicians, and
patients to improve outcomes, while meeting relevant health care
priorities and exploring burden reduction.
In response to increased mental health needs, including the need
for availability of inpatient psychiatric beds, we proposed changes to
Sec. 412.25(c) to allow greater flexibility for hospitals to open
excluded units, while minimizing the amount of effort Medicare
contractors would need to spend administering the regulatory
requirements. Although we are cognizant that there is need for mental
health services and support for providers along a continuum of care,
including a robust investment in community-based mental health
services, this proposal was focused on inpatient psychiatric facility
settings.
We proposed that changes to Sec. 412.25(c) would apply to both
IPFs and IRFs; therefore, revisions to Sec. 412.25(c) would also
affect IRFs in similar ways. Readers should refer to the FY 2024 IRF
PPS proposed rule (88 FR 20981 through 20984) for discussion of
proposed revisions to Sec. 412.25(c) and unique considerations
applicable to IRF units. As previously stated, the current requirements
at Sec. 412.25(c)(1) were originally established to manage the
administrative complexity associated with cost-based reimbursement for
excluded IPF and IRF units. Because IPF and IRF units are no longer
paid under cost-based reimbursement, but rather under the IPF PPS and
IRF PPS respectively, we believe that the restriction that limits an
IPF or IRF unit to being excluded only at the start of a cost reporting
period is no longer necessary. We amended our regulations in the FY
2012 IRF PPS final rule to address a regulation that, similarly, was
previously necessary for cost-based reimbursement, but was not material
to payment under the IRF PPS and IPF PPS. In that final rule, we
explained that under cost-based payments, the facilities' capital costs
were determined, in part, by their bed size and square footage. Changes
in the bed size and square footage would complicate the facilities'
capital cost allocation. We explained that under the IRF PPS and IPF
PPS, a facility's bed size and square footage were not relevant for
determining the individual facility's Medicare payment. Therefore, we
believed it was appropriate to modify some of the restrictions on a
facility's ability to change its bed size and square footage.
Accordingly, we relaxed the restrictions on a facility's ability to
increase its bed size and square footage. Under the revised
requirements that we adopted in the FY 2012 IRF PPS final rule at Sec.
412.25(b), an IRF or IPF can change (either increase or decrease) its
bed size or square footage one time at any point in a given cost
reporting period as long as it notifies the CMS Regional Office (RO) at
least 30 days before the date of the proposed change, and maintains the
information needed to accurately determine costs that are attributable
to the excluded units.
Similarly, in the case of the establishment of new excluded IPF and
IRF units, we do not believe that the timing of the establishment of
the new unit is material for determining the individual facility's
Medicare payment under the IPF PPS or IRF PPS. We believe it would be
appropriate to allow a unit to become excluded at any time in the cost
reporting year. However, we also believe it is important to minimize
the potential administrative complexity associated with units changing
their excluded status.
Accordingly, we proposed to modify the requirements currently in
regulation at Sec. 412.25(c)(1) to allow a hospital to change the
status of an IPF unit any time within the cost reporting year, as long
as the hospital notifies the CMS Regional Office and Medicare
Administrative Contractor (MAC) in writing of the change at least 30
days before the date of the change, and that this change would remain
in effect for the rest of that cost reporting year. We also proposed to
maintain the current requirements of Sec. 412.25(c)(2) which specify
that, if an excluded unit becomes not excluded during a cost reporting
year, the hospital must notify the MAC and CMS Regional Office in
writing of the change at least 30 days before the change, and this
change would remain in effect for the rest of that cost reporting year.
Finally, we proposed to consolidate the requirements for Sec.
412.25(c)(1) and Sec. 412.25(c)(2) into a new Sec. 412.25(c)(2) that
would apply to IPF units and
[[Page 51095]]
specify the requirements for an IPF unit to become excluded or not
excluded. We stated that we believed this proposal would provide
greater flexibility to hospitals to establish an excluded unit at a
time other than the start of a cost reporting period. We solicited
comments on the proposed changes.
Comment: We received unanimous commenter support on the proposal to
modify the requirements to allow a hospital to open a new IPF unit any
time within the cost reporting year, as long as the hospital notifies
the CMS Regional Office and MAC in writing of the change at least 30
days before the date of the change. Commenters were appreciative of how
this change would allow greater flexibility in how and when a unit
could be designated to be excluded or not from the IPPS. Commenters
also stated this change could alleviate the problem of limited bed
availability by allowing hospitals to be more responsive to the need
for inpatient psychiatric beds in their communities.
Response: We thank commenters for their support and agree this
modification will allow greater flexibility in how and when a unit
could be designated to be excluded from the IPPS. We also agree this
change will allow hospitals to be more responsive to the need for
inpatient psychiatric beds.
Comment: One commenter requested that CMS allow certain units that
have changed their status to change their status back at least one time
during the same cost reporting period. Specifically, they believe that
units that experience a status change on the first day of the cost
reporting period should have the opportunity to revert to their
original designation one time throughout the cost reporting period.
They further clarified that, if an IPF unit specifies and communicates
with the appropriate parties before the beginning of the next cost
reporting year that it would want to reclassify, and then when the cost
reporting period begins decides to revert, it should be allowed the
opportunity to make the necessary changes.
Response: We do not fully understand the commenter's concern, but
we believe the commenter is seeking clarification about whether a
hospital unit would be permitted to change its status during the cost
reporting year to revert to the status it held during the prior year.
Under the proposed policy, a hospital unit would be permitted to change
its status to either excluded or not excluded only one time during the
cost reporting year, and would be required to maintain that status
until the end of the cost reporting year. We are clarifying that
changes made at the beginning of a cost reporting year would not limit
the ability of the hospital unit to make a one-time status change
during the same cost reporting year. Therefore, if the hospital unit
starts the cost reporting year as excluded, it could become not
excluded at any time during the cost reporting year; if the hospital
unit starts the cost reporting year as not excluded, it could become
excluded at any time during the cost reporting year.
Final Decision: After consideration of the comments received, we
are finalizing our proposal to modify the requirements currently in
regulation at Sec. 412.25(c)(1) to allow a hospital to change the
status of an IPF unit from not excluded to excluded any time within the
cost reporting year. We are also finalizing as proposed that a hospital
will be required to notify the CMS Regional Office and MAC in writing
of the change at least 30 days before the date of the change, and that
this change would remain in effect for the rest of that cost reporting
year. In addition, we are finalizing our proposal to maintain the
current requirements of Sec. 412.25(c)(2), which specify that, if an
excluded unit becomes not excluded during a cost reporting year, the
hospital must notify the MAC and CMS Regional Office in writing of the
change at least 30 days before the change, and this change would remain
in effect for the rest of that cost reporting year.
Lastly, we proposed an identical policy for rehabilitation units of
hospitals in the FY 2024 IRF PPS proposed rule, specifying that the
regulatory provision that would pertain to IRF units would appear in
Sec. 412.25(c)(1). We proposed discrete regulation text for each of
the hospital unit types (that is, IRF units and IPF units) in order to
solicit comments on issues that might impact one hospital unit type and
not the other. We also stated that we may consider adopting one
consolidated regulations text for both IRF and IPF units in the final
rules if we finalize both of our proposals. We did not receive any
comments regarding a consolidated regulation for both IRF and IPF
units; nor did commenters raise any issues that would impact one
hospital unit type and not the other. We are finalizing a consolidated
regulation at Sec. 412.25(c) that applies to both IPF hospital units
and IRF hospital units.
V. Existing Data Collection and Request for Information (RFI) To Inform
Revisions to the IPF PPS as Required by the CAA, 2023
A. Changes to IPF PPS in the CAA, 2023
As discussed in section IV.C.1 of this final rule, we proposed to
continue using the existing regression-derived IPF PPS adjustment
factors for FY 2024. In the FY 2023 IPF PPS proposed rule (87 FR 19428
through 19429), we discussed the background of these current IPF PPS
patient-level and facility-level adjustment factors, which are the
regression-derived adjustment factors from the November 15, 2004 IPF
PPS final rule and briefly discussed past analyses and areas of concern
for future refinement, about which we previously solicited comments.
Finally, in the FY 2023 proposed rule, we described the results of the
latest analysis of the IPF PPS, which were summarized in a technical
report posted to the CMS website \3\ accompanying the rule and
solicited comments on certain topics from the report.
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\3\ https://www.cms.gov/files/document/technical-report-medicare-program-inpatient-psychiatric-facilities-prospective-payment-system.pdf.
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Section 4125 of the CAA, 2023 amended section 1886(s) of the Act to
add new paragraph 1886(s)(5), which requires revisions to the
methodology for determining the payment rates under the IPF PPS for FY
2025 and future years as the Secretary determines appropriate.
Specifically, new section 1886(s)(5)(A) of the Act requires the
Secretary to collect data and information as the Secretary as
determines appropriate to revise payments under the IPF PPS. This data
collection is required to begin no later than October 1, 2023, which is
the start of FY 2024. In addition, new section 1886(s)(5)(D) of the Act
requires that the Secretary implement by regulation revisions to the
methodology for determining the payment rates for psychiatric hospitals
and psychiatric units (that is, under the IPF PPS), for rate year 2025
(FY 2025) and for subsequent years if the Secretary determines it
appropriate. The revisions may be based on a review of the data and
information collection.
As noted above, section 1886(s)(5)(A) of the Act requires the
Secretary to begin collecting, by not later than October 1, 2023, data
and information as appropriate to inform revisions to the IPF PPS. New
section 1886(s)(5)(B) of the Act, as added by the CAA, 2023 lists the
following types of data and information as a non-exhaustive list of
[[Page 51096]]
examples of what may be collected under this authority:
Charges, including those related to ancillary services;
The required intensity of behavioral monitoring, such as
cognitive deficit, suicidal ideations, violent behavior, and need for
physical restraint; and
Interventions, such as detoxification services for
substance abuse, dependence on respirator, total parenteral nutritional
support, dependence on renal dialysis, and burn care.
We note that our extensive years-long and ongoing data collection
efforts are consistent with the types of data the CAA, 2023 suggests we
might collect as well as the purpose for which the CAA, 2023 requires
the data collection, as described in the following paragraphs.
B. Current Data and Information Collection Requirements
1. Charges, Including Those Related to Ancillary Services
As specified at 42 CFR 413.20, hospitals are required to file cost
reports on an annual basis and maintain sufficient financial records
and statistical data for proper determination of costs payable under
the Medicare program. Currently, IPFs and psychiatric units are
required to report ancillary charges on cost reports.
In general, most providers allocate their Medicare costs using
costs and charges as described at 42 CFR 413.53(a)(1)(i) and referred
to as the Departmental Method. For cost reporting periods beginning on
or after October 1, 1982, the Departmental Method, which is the ratio
of beneficiary charges to total patient charges for the services of
each ancillary department, is applied to apportion the cost of the
department. Added to this amount is the cost of routine services for
program beneficiaries, determined on the basis of a separate average
cost per diem for all patients for general routine patient care areas
as required at Sec. 413.53(a)(1)(i) and (e).
The Departmental Method for apportioning allowable cost between
Medicare and non-Medicare patients under the program is not readily
adaptable to those hospitals that do not have a charge structure.
Current cost reporting rules allow hospitals that do not have a charge
structure to file an all-inclusive cost report using an alternative
cost allocation method. These alternative methods as described in the
CMS Pub. 15-1, chapter 22 of the Provider Reimbursement Manual (PRM),
Methods A, B and E, in order of preference, must be approved by the MAC
after considering the data available and ascertaining which method can
be applied to achieve equity, not merely greater reimbursement, in the
allocation of costs for services rendered to Medicare beneficiaries.
Method A (Departmental Statistical Method) is used in the absence
of charge data and where adequate departmental statistics are
available. Where Method A was not used, the MAC may have granted
specific permission for a hospital to continue to use on a temporary
basis a less sophisticated Method B (Sliding Scale) or E (Percentage of
Per Diem). A provider that elects and is approved under Method A, may
not change to a Method B or E in a subsequent year. These alternative
methods of apportionment are limited and available only to those
hospitals that do not and never have had a charge structure for
individual services rendered. Historically, most hospitals that were
approved to file all-inclusive cost reports were Indian Health Services
hospitals, government-owned psychiatric and acute care hospitals, and
nominal charge hospitals.
In the FY 2016 IPF PPS final rule (80 FR 46693 through 46694), we
discussed analysis conducted to better understand IPF industry
practices for future IPF PPS refinements. This analysis revealed that
in 2012 to 2013, over 20 percent of IPF stays show no reported
ancillary costs, such as laboratory and drug costs, on cost reports or
charges on claims. In the FY 2016 IPF PPS final rule (80 FR 46694), FY
2017 IPF PPS final rule (81 FR 50513), FY 2018 IPF PPS final rule (82
FR 36784), FY 2019 IPF PPS final rule (83 FR 38588) and FY 2020 IPF PPS
final rule (84 FR 38458), we reminded providers that we pay only the
IPF for services furnished to a Medicare beneficiary who is an
inpatient of that IPF, except for certain professional services, and
payments are considered to be payments in full for all inpatient
hospital services provided directly or under arrangement (see 42 CFR
412.404(d)), as specified in 42 CFR 409.10.
On November 17, 2017, we issued Transmittal 12, which made changes
to the hospital cost report form CMS-2552-10 (OMB No. 0938-0050), and
included cost report Level I edit 10710S, effective for cost reporting
periods ending on or after August 31, 2017. Edit 10710S required that
cost reports from psychiatric hospitals include certain ancillary
costs, or the cost report will be rejected. On January 30, 2018, we
issued Transmittal 13, which changed the implementation date for
Transmittal 12 to be for cost reporting periods ending on or after
September 30, 2017. CMS suspended edit 10710S effective April 27, 2018,
pending evaluation of the application of the edit to all-inclusive-rate
providers. CMS issued Transmittal 15 on October 19, 2018, reinstating
the requirement that cost reports from psychiatric hospitals, except
all-inclusive rate providers, include certain ancillary costs. For
details, we refer readers to see these Transmittals, which are
available on the CMS website at https://www.cms.gov/regulations-and-guidance/guidance/transmittals.
2. Required Intensity of Behavioral Monitoring and Interventions
As discussed in the November 2004 IPF PPS final rule (69 FR 66946),
we encourage IPFs to code all diagnoses requiring active treatment
during the IPF stay. These include ICD-10-CM codes that indicate the
required intensity of behavioral monitoring, such as cognitive deficit,
suicidal ideations, violent behavior, and need for physical restraint.
The IPF PPS includes comorbidity and MS-DRG adjustment factors that
increase IPF PPS payment for stays that include these codes. For
example, ICD-10-CM codes X71 through X83 indicate self-harm. ICD-10-CM
codes under R45 indicate emotional state including violent behavior.
These and other ICD-10-CM codes indicate the required intensity of
behavioral monitoring and should be reported on the IPF claims, if
applicable.
The presence of certain ICD-10-CM codes as a principal or comorbid
condition is used to adjust IPF PPS payments to reflect the resource
intensity associated with these conditions. For example, codes that
group to MS-DRG 884 Organic Disturbances & Intellectual Disabilities,
and codes that are included in the IPF comorbidity category for
Developmental Disabilities, result in increased payment for IPF stays
for patients with cognitive deficit.
As we further discussed in the November 2004 IPF PPS final rule (69
FR 66938 through 66944), we developed comorbidity categories based on
the clinical expertise of physicians to identify conditions that would
require comparatively more costly treatment during an IPF stay than
other comorbid conditions. We used a regression analysis of
administrative claims and cost report data to determine the adjustment
factors associated with each comorbidity category. In addition, we used
the same regression analysis to determine the adjustment factors
associated with the 17 MS-DRGs that are included for payment
adjustments
[[Page 51097]]
under the IPF PPS (as identified in Addendum A). As discussed in
section IV.C.2.b of this final rule, we routinely update the ICD-10-CM
codes that are included in the MS-DRGs and comorbidity categories.
We also collect relevant demographic information such as patient
age, and we collect information and adjust payment based on the length
of IPF stays. Each of these adjustments reflects the difference in
service intensity, as measured by increased or decreased costs, for
different patients over the course of an IPF stay.
In addition, IPFs and psychiatric units report on claims the ICD-
10-PCS codes for interventions including oncology treatment procedures,
which is used for adjusting payment under the oncology comorbidity
category, and ECT, which is paid for using a per treatment amount as
discussed in section IV.B.2 of this final rule. Other ICD-10-CM
diagnosis codes indicate the need for certain interventions, such as
detoxification services or substance abuse (for example, F10.121, which
is included in the drug and alcohol abuse comorbidity category),
dependence on respirator (for example, Z99.11 included in the COPD
category), and dependence on renal dialysis (for example, Z99.2
included in the chronic renal failure category). We note that the IPS
PPF does not currently adjust for burn care but recognize there are
ICD-10-CM/PCS codes that denote conditions and procedures related to
burn care. As discussed in the previous paragraph, the IPF PPS includes
comorbidity adjustments that reflect the higher relative costs for
active treatment of these conditions. IPF patients with these
conditions are costlier to treat primarily because of the costs
associated with interventions and longer lengths of stay.
3. Request for Information on Data and Information Collection
As noted in section V.A of this final rule, our extensive years-
long and ongoing data collection efforts are consistent with the types
of data that the CAA, 2023 suggests we might collect, as well as aligns
with the purpose for which the CAA, 2023 requires the data collection.
In this final rule, we are requesting information from the public to
inform revisions to the IPF PPS required by section 4125(a) of the CAA,
2023. We are seeking information about specific additional data and
information psychiatric hospitals and psychiatric units might report
that could be appropriate and useful to help inform possible revisions
to the methodology for payment rates under the IPF PPS for FY 2025 and
future years if determined appropriate by the Secretary.
Section 1886(s)(5)(C) of the Act provides that the Secretary may
collect additional data and information on cost reports, claims, or
otherwise. Therefore, we also sought information about potential
available data and information sources, including using additional
elements of the current cost reports, claims, or other sources, taking
into consideration factors such as the timing and availability of data,
the quality of the potential data and information to be collected, and
the potential administrative burden on providers, MACs, and CMS.
We solicited comment on the following topics:
What other data and information would be beneficial for
informing revisions to the IPF PPS payment methodologies that are
currently obtainable through claims or cost report information? What
codes, conditions, or other indicators should we examine in order to
potentially identify this data from existing sources?
What other data and information would be beneficial for
informing revisions to the IPF PPS payment methodologies that are not
routinely coded on claims or identifiable through cost report
information? What are some potential alternative sources we could
consider for collecting these data and information?
What data and information that is currently reported on
claims data could be used to inform revisions to the IPF PPS payment
methodologies?
As we discussed in the FY 2024 IPF PPS proposed rule, the
current IPF PPS payment adjustments were derived from a regression
analysis based on the FY 2002 MedPAR data file. The adjustment factors
included for payment were found in the regression analysis to be
associated with statistically significant per diem cost differences;
with statistical significance defined as p less than 0.05. Are there
alternative methodological approaches or considerations that we should
consider for future analysis?
What if any additional data or information should we
consider collecting that could address access to care in rural and
isolated communities?
4. Request for Information About Charges for Ancillary Services
In conjunction with the FY 2023 IPF PPS proposed rule (87 FR 19428
through 19429), we posted a report on the CMS website that summarizes
the results of the latest analysis of more recent IPF cost and claim
information for potential IPF PPS adjustments and requested comments
about the results summarized in the report. That report showed that
approximately 23 percent of IPF stays were trimmed from the data set
used in that analysis because they were stays at facilities where fewer
than 5 percent of their stays had ancillary charges. This report is
available online at https://www.cms.gov/medicare/inpatient-psychiatric-facility-pps/ipf-reports-and-educational-resources.
In response to the comment solicitation, we received a comment from
MedPAC regarding facilities that do not report ancillary charges on
most or any of their claims. Ancillary services are the services for
which charges are customarily made in addition to routine services.
These include services such as labs, drugs, radiology, physical and
occupational therapy services, and other types of services that
typically vary between stays. Generally, based on the nature of IPF
services and the conditions of participation \4\ applicable to IPFs, we
expect to see ancillary services and correlating charges, such as labs
and drugs, on most IPF claims. Our ongoing analysis has found that
certain providers, especially for-profit freestanding IPFs, are
consistently reporting no ancillary charges or very minimal ancillary
charges. MedPAC stated that it is not known: whether IPFs fail to
report ancillary charges separately because they were appropriately
bundled with all other charges into an all-inclusive per diem rate; if
no ancillary charges were incurred because the IPF cares for a patient
mix with lower care needs or inappropriately stints on care; or if
ancillary charges for services furnished during the IPF stay are
inappropriately billed outside of the IPF base rate (unbundling).
MedPAC recommended CMS conduct further investigation into the lack of
certain ancillary costs and charges and whether IPFs are providing
necessary care and appropriately billing for inpatient psychiatric
services under the IPF PPS.
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\4\ IPFs are subject to all hospital conditions of
participation, including 42 CFR 482.25, which specifies that ``The
hospital must have pharmaceutical services that meet the needs of
the patients,'' and 482.27, which specifies that ``The hospital must
maintain, or have available, adequate laboratory services to meet
the needs of its patients.''
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As discussed in the previous section of this FY 2024 IPF PPS final
rule, we requested information related to the specific types of data
and information specified in the CAA, 2023, including the reporting of
charges for ancillary services, such as labs and drugs, on IPF claims.
We are interested in better understanding IPF industry practices
[[Page 51098]]
pertaining to the billing and provision of ancillary services to inform
future IPF PPS refinements. We are considering whether to require
charges for ancillary services to be reported on claims and potentially
reject claims if no ancillary services are reported, and whether to
consider payment for such claims to be inappropriate or erroneous and
subject to recoupment. Accordingly, we solicited comments on the
following questions:
What would be the appropriate level of ancillary charges
CMS should expect to be reported on claims? Are there specific reasons
that an IPF stay would include no ancillary services?
What are the reasons that some providers are not reporting
ancillary charges on their claims?
Would it be appropriate for CMS to require and reject
claims if there are no ancillary charges reported? Or should CMS
consider adjusting payment to providers that do not report ancillary
charges on their claims? For example, does the lack of ancillary
charges on claims suggest a lack of reasonable and necessary treatment
during the IPF stay, and would it be appropriate for CMS to only apply
the IPF PPS patient-level adjustment factors for claims that include
ancillary charges?
C. Social Drivers of Health
Social drivers of health (SDOH), also known as social determinants
of health, are the conditions in the environments where people are
born, live, learn, work, play, worship, and age that affect a wide
range of health, functioning, and quality-of-life outcomes and
risks.\5\ Studies have shown that there is a correlation between the
effects of low income and education and overall health status. One
study derived that the lowest income and least educated individuals
were consistently least healthy.\6\ We have previously demonstrated our
commitment to advancing health equity and reducing health disparities.
In the past, and in our ongoing efforts, we have strived to identify
and implement policies, procedures, reporting protocols, and other
initiatives in a number of our programs that address the impact of SDOH
on an individual's health.
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\5\ https://health.gov/healthypeople/priority-areas/social-determinants-health.
\6\ Paula A. Braveman, Catherine Cubbin, Susan Egerter, David R.
Williams, and Elsie Pamuk, 2010:
Socioeconomic Disparities in Health in the United States: What
the Patterns Tell Us American Journal of Public Health 100,
S186_S196, https://doi.org/10.2105/AJPH.2009.166082.
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For the IPF Quality Reporting Program, as discussed in section VI.D
below of this final rule, we are adopting the Facility Commitment to
Health Equity measure for the FY 2026 payment determination and
subsequent years, the Screening for Social Drivers of Health measure
beginning with voluntary reporting of data reflecting care provided in
2024 beginning in CY 2025 with required reporting for the FY 2027
payment determination and subsequent years, and the Screen Positive
Rate for Social Drivers of Health measure beginning with voluntary
reporting of data beginning in CY 2024 with required reporting for the
FY 2027 payment determination and subsequent years.
Additionally, in the technical report \7\ accompanying the FY 2023
IPF PPS proposed rule, we explained that we analyzed the costs
associated with SDOH but found that our analysis was confounded by a
low frequency of IPF claims reporting the applicable ICD-10 diagnosis
codes. In response to the FY 2023 IPF PPS proposed rule we received 10
comments pertaining to the report on the analysis of patient-level and
facility-level adjustment factors, and areas of interest for further
research, including additional SDOH analysis.
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\7\ https://www.cms.gov/files/document/technical-report-medicare-program-inpatient-psychiatric-facilities-prospective-payment-system.pdf.
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Working in collaboration with a contractor, subsequent analysis has
shown that other SDOH codes, such as Z59.9 Problem related to housing
and economic circumstances, unspecified, are associated with
statistically significant, higher costs. In general, our analysis found
that claims that included SDOH codes had lower costs than claims that
did not include such codes. This finding is counterintuitive; however,
we note that studies have found that there are disparities in the
reporting of SDOH codes, such as homelessness.\8\ Additionally, our
analysis found that certain codes were associated with increased cost
for IPF treatment. Specifically, the below SDOH codes in the analysis
were found to be statistically significant and had a stay count of
greater than 100. These codes had an adjustment factor above 1,
suggesting that these conditions may increase relative costliness of
IPF stays:
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\8\ https://aspe.hhs.gov/reports/health-conditions-among-individuals-history-homelessness-research-brief-0.
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Z559 Problems related to education and literacy,
unspecified.
Z599 Problems related to housing and economic
circumstances, unspecified.
Z600 Problems of adjustment to life-cycle transitions.
Z634 Disappearance and death of family member.
Z653 Problems related to other legal circumstances.
Z659 Problems related to unspecified psychosocial
circumstances.
We solicited comments on these findings and information about
whether it would be appropriate to consider incorporating these codes
into the IPF PPS in the future, for example as a patient-level
adjustment. Specifically, for codes that are ``unspecified,'' we sought
information about what types of conditions or circumstances these codes
might represent. We sought any information that commenters could
provide about the reasons for including these codes on claims. We also
requested information on what factors commenters believe we should
consider in order to better understand the cost regression results
presented above.
D. Public Comments Received in Response to CY 2024 IPF PPS Proposed
Rule
We received 15 comments in response to the FY 2024 IPF PPS proposed
rule pertaining to existing and future data collection to inform
revisions to the IPF PPS as required by the CAA, 2023. Commenters
offered various suggestions of patient characteristics and factors we
could consider for analysis. Commenters included MedPAC, state-level
and national provider and patient advocacy organizations, and health
systems.
We thank commenters for their detailed responses to this comment
solicitation. We will take these comments into consideration to
potentially inform future rulemaking.
VI. Inpatient Psychiatric Facility Quality Reporting (IPFQR) Program
A. Background and Statutory Authority
The Inpatient Psychiatric Facility Quality Reporting (IPFQR)
Program is authorized by section 1886(s)(4) of the Act, and it applies
to psychiatric hospitals and psychiatric units paid by Medicare under
the IPF PPS (see section VI.B. of this final rule). Section
1886(s)(4)(A)(i) of the Act requires the Secretary to reduce by 2
percentage points the annual update to the standard federal rate for
discharges for the IPF occurring during such fiscal year \9\ for
[[Page 51099]]
any IPF that does not comply with quality data submission requirements
under the IPFQR Program, set forth in accordance with section
1886(s)(4)(C) of the Act, with respect to an applicable fiscal year.
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\9\ We note that the statute uses the term ``rate year'' (RY).
However, beginning with the annual update of the inpatient
psychiatric facility prospective payment system (IPF PPS) that took
effect on July 1, 2011 (RY 2012), we aligned the IPF PPS update with
the annual update of the ICD codes, effective on October 1 of each
year. This change allowed for annual payment updates and the ICD
coding update to occur on the same schedule and appear in the same
Federal Register document, promoting administrative efficiency. To
reflect the change to the annual payment rate update cycle, we
revised the regulations at 42 CFR 412.402 to specify that, beginning
October 1, 2012, the IPF PPS RY means the 12-month period from
October 1 through September 30, which we refer to as a ``fiscal
year'' (FY) (76 FR 26435). Therefore, with respect to the IPFQR
Program, the terms ``rate year,'' as used in the statute, and
``fiscal year'' as used in the regulation, both refer to the period
from October 1 through September 30. For more information regarding
this terminology change, we refer readers to section III of the RY
2012 IPF PPS final rule (76 FR 26434 through 26435).
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Section 1886(s)(4)(C) of the Act requires IPFs to submit to the
Secretary data on quality measures specified by the Secretary under
section 1886(s)(4)(D) of the Act. Except as provided in section
1886(s)(4)(D)(ii) of the Act, section 1886(s)(4)(D)(i) of the Act
requires that any measure specified by the Secretary must have been
endorsed by the consensus-based entity (CBE) with a contract under
section 1890(a) of the Act. Section 1886(s)(4)(D)(ii) of the Act
provides that, in the case of a specified area or medical topic
determined appropriate by the Secretary for which a feasible and
practical measure has not been endorsed by the CBE with a contract
under section 1890(a) of the Act, the Secretary may specify a measure
that is not endorsed as long as due consideration is given to measures
that have been endorsed or adopted by a consensus organization
identified by the Secretary.
We refer readers to the FY 2019 IPF PPS final rule (83 FR 38589)
for a more detailed discussion of the background and statutory
authority of the IPFQR Program.
For the IPFQR Program, we refer to the year in which an IPF would
receive the 2-percentage point reduction to the annual update to the
standard federal rate as the payment determination year. An IPF
generally meets IPFQR Program requirements by submitting data on
specified quality measures in a specified time and manner during a data
submission period that occurs prior to the payment determination year.
These data reflect a period prior to the data submission period during
which the IPF furnished care to patients; this period is known as the
performance period. For example, for a measure affecting FY 2026
payment determination, for which CY 2024 is the performance period and
for which data are required to be submitted in CY 2025, if an IPF did
not submit the data for this measure as specified during CY 2025 (even
if the IPF meets all other IPFQR Program requirements for the FY 2026
payment determination) we would reduce by 2-percentage points that
IPF's update for the FY 2026 payment determination year.
In the FY 2024 IPF PPS proposed rule (88 FR 21273), we proposed to
codify the IPFQR Program requirements governing IPF reporting on
quality measures in a new regulation at Sec. 412.433, which is the
section preceding our existing regulation governing reconsideration and
appeals procedures for IPFQR Program decisions in our regulations at
Sec. 412.434. Specifically, we proposed to codify a general statement
of the IPFQR Program authority and structure at Sec. 412.433(a).
Paragraph (a) will cite section 1886(s)(4) of the Act, which requires
the Secretary to implement a quality reporting program for inpatient
psychiatric hospitals and psychiatric units. Paragraph (a) will also
state that IPFs paid under the IPF PPS as provided in section
1886(s)(1) of the Act that do not report data required for the quality
measures selected by the Secretary in a form and manner, and at a time
specified by the Secretary will incur a 2.0 percentage point reduction
to the annual update to the standard federal rate with respect to the
applicable fiscal year.
We solicited comments on this proposal.
Comment: One commenter requested clarification regarding whether
there are penalties for facilities that do not meet all the reporting
requirements for a specific year.
Response: The IPFQR Program is a pay-for-reporting program. IPFs
are not, and will not be, penalized based on their performance on
measures reported to CMS as part of the IPFQR Program. However, if an
IPF does not comply with quality data submission requirements under the
IPFQR Program for a given fiscal year, section 1886(s)(4)(A)(i) of the
Act requires the Secretary to reduce by 2 percentage points the annual
update to the standard federal rate for discharges for the IPF
occurring during such fiscal year.
We specifically proposed to codify established IPFQR Program
requirements, particularly those set forth in the statute at section
1886(s)(4) of the Act and our prior rulemaking, in a new regulation at
Sec. 412.433. Our proposal to codify penalties for an IPF's failure to
submit data as required by the IPFQR Program at Sec. 412.433(a) merely
reiterates the penalty already required by the statute set forth at
section 1886(s)(4) of the Act.
Final Decision: After consideration of the public comments we
received, we are finalizing codification of the IPFQR Program
requirements governing IPF reporting on quality measures at a new
regulation at Sec. 412.433. We are finalizing the regulation text as
proposed except that we are correcting one typographical error in which
the ``Act'' was inadvertently referred to as the ``act.''
B. Covered Entities
In the FY 2013 IPPS/LTCH PPS final rule (77 FR 53645), we
established that the IPFQR Program's quality reporting requirements
cover those psychiatric hospitals and psychiatric units paid by
Medicare under IPF PPS in accordance with Sec. 412.404(b). Generally,
psychiatric hospitals and psychiatric units within acute care and
critical access hospitals (CAHs) that treat Medicare patients are paid
under the IPF PPS. Consistent with previous regulations, we continue to
use the terms ``facility'' or ``IPF'' to refer to both inpatient
psychiatric hospitals and psychiatric units. This usage follows the
terminology in our IPF PPS regulations at Sec. 412.402. For more
information on covered entities, we refer readers to the FY 2013 IPPS/
LTCH PPS final rule (77 FR 53645).
C. Previously Finalized Measures
The current IPFQR Program includes 14 measures for the FY 2024
payment determination. For more information on these measures, we refer
readers to Table 20 of this final rule (see section VI.G of this final
rule).
D. Measure Adoption
We strive to put patients and caregivers first, ensuring they are
empowered to partner with their clinicians in their healthcare
decision-making using information from data-driven insights that are
increasingly aligned with meaningful quality measures. We support
technology that reduces burden and allows clinicians to focus on
providing high-quality healthcare for their patients. We also support
innovative approaches to improve quality, accessibility, and
affordability of care while paying particular attention to improving
clinicians' and beneficiaries' experiences when interacting with our
programs. In combination with other efforts across HHS, we believe the
IPFQR Program helps to incentivize IPFs to improve healthcare quality
and value while giving patients and providers the tools and information
needed to make the best individualized decisions. Consistent with these
goals, our objective in selecting quality
[[Page 51100]]
measures for the IPFQR Program is to balance the need for information
on the full spectrum of care delivery and the need to minimize the
burden of data collection and reporting. We have primarily focused on
measures that evaluate critical processes of care that have significant
impact on patient outcomes and support CMS and HHS priorities for
improved quality and efficiency of care provided by IPFs. When
possible, we also propose to incorporate measures that directly
evaluate patient outcomes and experience.
We refer readers to the CMS National Quality Strategy,\10\ the
Behavioral Health Strategy,\11\ the Framework for Health Equity,\12\
and the Meaningful Measures Framework \13\ for information related to
our priorities in selecting quality measures.
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\10\ Schreiber, M, Richards, A, et al. (2022). The CMS National
Quality Strategy: A Person-Centered Approach to Improving Quality.
Available at: https://www.cms.gov/blog/cms-national-quality-strategy-person-centered-approach-improving-quality. Accessed on
February 20, 2023.
\11\ CMS. (2022). CMS Behavioral Health Strategy. Available at
https://www.cms.gov/cms-behavioral-health-strategy. Accessed on
February 20, 2023.
\12\ CMS. (2022). CMS Framework for Health Equity 2022-2032.
Available at https://www.cms.gov/files/document/cms-framework-health-equity-2022.pdf. Accessed on February 20, 2023.
\13\ CMS. (2022). Meaningful Measures 2.0: Moving from Measure
Reduction to Modernization. Available at https://www.cms.gov/medicare/meaningful-measures-framework/meaningful-measures-20-moving-measure-reduction-modernization. Accessed on February 20,
2023.
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1. Measure Selection Process
Section 1890A of the Act requires that the Secretary establish and
follow a pre-rulemaking process, in coordination with the consensus-
based entity (CBE) with a contract under section 1890 of the Act, to
solicit input from certain groups regarding the selection of quality
and efficiency measures for the IPFQR Program. Before being proposed
for inclusion in the IPFQR Program, measures are placed on a list of
Measures Under Consideration (MUC) list, which is published annually on
behalf of CMS by the consensus-based entity (CBE),\14\ with which the
Secretary must contract as required by section 1890(a) of the Act.
Following publication on the MUC list, a multi-stakeholder group
convened by the CBE reviews the measures under consideration for the
IPFQR Program, among other federal programs, and provides input on
those measures to the Secretary. We consider the input and
recommendations provided by this multi-stakeholder group in selecting
all measures for the IPFQR Program.
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\14\ In previous years, we referred to the consensus-based
entity by corporate name. We have updated this language to refer to
the consensus-based entity more generally.
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Information about the multi-stakeholder group's input on each of
our newly adopted measures is described in the following subsections.
In our evaluation of the IPFQR Program measure set, we identified four
measures that we believe are appropriate for adoption for the IPFQR
Program:
Facility Commitment to Health Equity;
Screening for Social Drivers of Health;
Screen Positive Rate for Social Drivers of Health; and
Psychiatric Inpatient Experience (PIX) Survey.
These four measures are described in the following subsections.
2. Adoption of the Facility Commitment to Health Equity Measure
Beginning With the CY 2024 Reporting Period (Data Submitted in CY
2025)/FY 2026 Payment Determination
a. Background
Significant and persistent disparities in healthcare outcomes exist
in the United States. For example, belonging to a racial or ethnic
minority group, living with a disability, being a member of the
lesbian, gay, bisexual, transgender, and queer (LGBTQ+) community,
being a member of a religious minority, living in a rural area, or
being near or below the poverty level, is often associated with worse
health outcomes.15 16 17 18 19 20 21 22 23 24 Numerous
studies have shown that among Medicare beneficiaries, racial and ethnic
minority individuals often receive clinical care of lower quality,
report having worse care experiences, and experience more frequent
hospital readmissions and procedural
complications.25 26 27 28 29 30 Readmission rates in the
Hospital Readmissions Reduction Program have been shown to be higher
among Black and Hispanic Medicare beneficiaries with common
[[Page 51101]]
conditions, including congestive heart failure and acute myocardial
infarction. 31 32 33 34 35 Data indicate that, even after
accounting for factors such as socioeconomic conditions, members of
racial and ethnic minority groups reported experiencing lower quality
of healthcare.\36\ Evidence of differences in quality of care received
among people from racial and ethnic minority groups shows worse health
outcomes, including a higher incidence of diabetes complications such
as retinopathy.\37\ Additionally, inequities in the social drivers of
health (SDOH) affecting these groups, such as poverty and healthcare
access, are interrelated and influence a wide range of health and
quality-of-life outcomes and risks.\38\
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\15\ Joynt KE, Orav E, Jha AK. (2011). Thirty-Day Readmission
Rates for Medicare Beneficiaries by Race and Site of Care. JAMA,
305(7), 675-681. Available at: https://jamanetwork.com/journals/jama/fullarticle/645647. Accessed on February 13, 2023.
\16\ Lindenauer PK, Lagu T, Rothberg MB, et al. (2013). Income
Inequality and Thirty-Day Outcomes After Acute Myocardial
Infarction, Heart Failure, and Pneumonia: Retrospective Cohort
Study. BMJ, 346. Available at: https://doi.org/10.1136/bmj.f521.
Accessed on February 13, 2023.
\17\ Trivedi AN, Nsa W, Hausmann LRM, et al. (2014). Quality and
Equity of Care in U.S. Hospitals. N Engl J Med, 371(24), 2298-2308.
Available at: https://www.nejm.org/doi/10.1056/NEJMsa1405003.
Accessed on February 13, 2023.
\18\ Polyakova, M, Udalova V, et al. (2021). Racial Disparities
In Excess All-Cause Mortality During The Early COVID-19 Pandemic
Varied Substantially Across States. Health Affairs, 40(2), 307-316.
Available at: https://doi.org/10.1377/hlthaff.2020.02142. Accessed
on February 14, 2023.
\19\ Rural Health Research Gateway. (2018). Rural Communities:
Age, Income, and Health Status. Rural Health Research Recap.
Available at: https://www.ruralhealthresearch.org/assets/2200-8536/rural-communities-age-income-health-status-recap.pdf. Accessed on
February 14, 2023.
\20\ HHS Office of Minority Health. (2020). Progress Report to
Congress, 2020 Update on the Action Plan to Reduce Racial and Ethnic
Health Disparities. Department of Health and Human Services.
Available at: https://www.minorityhealth.hhs.gov/assets/PDF/Update_HHS_Disparities_Dept-FY2020.pdf . Accessed on February 14,
2023.
\21\ Heslin KC, Hall JE. (2021). Sexual Orientation Disparities
in Risk Factors for Adverse COVID-19 Related Outcomes, by Race/
Ethnicity--Behavioral Risk Factor Surveillance System, United
States, 2017-2019. MMWR Morb Mortal Wkly Rep, 70(5), 149. Available
at: https://www.cdc.gov/mmwr/volumes/70/wr/mm7005a1.htm. Accessed on
February 14, 2023.
\22\ Poteat TC, Reisner SL, Miller M, Wirtz AL. (2020). COVID-19
Vulnerability of Transgender Women With and Without HIV Infection in
the Eastern and Southern U.S. medRxiv. Available at: https://www.medrxiv.org/content/10.1101/2020.07.21.20159327v1.full.pdf.
Accessed on February 14, 2023.
\23\ Vu M, Azmat A, Radejko T, Padela AI. (2016). Predictors of
Delayed Healthcare Seeking Among American Muslim Women. Journal of
Women's Health, 25(6), 586-593. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5912720/. Accessed on February
14, 2023.
\24\ Nadimpalli SB, Cleland CM, Hutchinson MK, Islam N, Barnes
LL, Van Devanter N. (2016). The Association Between Discrimination
and the Health of Sikh Asian Indians. Health Psychology, 35(4), 351-
355. Available at: https://doi.org/10.1037/hea0000268. Accessed o n
February 14, 2023.
\25\ CMS Office of Minority Health. (2020). Racial, Ethnic, and
Gender Disparities in Healthcare in Medicare Advantage. Baltimore,
MD: Centers for Medicare & Medicaid Services. Available at: https://www.cms.gov/files/document/2020-national-level-results-race-ethnicity-and-gender-pdf.pdf Accessed on February 14, 2023.
\26\ CMS Office of Minority Health. (2018). Guide to Reducing
Disparities in Readmissions. Available at: https://www.cms.gov/About-CMS/Agency-Information/OMH/Downloads/OMH_Readmissions_Guide.pdf. Accessed on February 14, 2023.
\27\ Singh JA, Lu X, et al. (2014). Racial Disparities in Knee
and Hip Total Joint Arthroplasty: An 18-year analysis of national
Medicare data. Ann Rheum Dis., 73(12), 2107-15. Available at:
https://ard.bmj.com/content/73/12/2107.full. Accessed on February
14, 2023.
\28\ Rivera-Hernandez M, Rahman M, Mor V, Trivedi AN. (2019).
Racial Disparities in Readmission Rates among Patients Discharged to
Skilled Nursing Facilities. J Am Geriatr Soc., 67(8), 1672-1679.
Available at: https://doi.org/10.1111/jgs.15960. Accessed on
February 14, 2023.
\29\ Joynt KE, Orav E, Jha AK. (2011). Thirty-Day Readmission
Rates for Medicare Beneficiaries by Race and Site of Care. JAMA,
305(7), 675-681. Available at: https://jamanetwork.com/journals/jama/fullarticle/645647. Accessed on February 13, 2023.
\30\ Tsai TC, Orav EJ, Joynt KE. (2014). Disparities in Surgical
30-day Readmission Rates for Medicare Beneficiaries by Race and Site
of Care. Ann Surg., 259(6), 1086-1090. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107654/. Accessed on February
14, 2023.
\31\ Rodriguez F, Joynt KE, Lopez L, Saldana F, Jha AK. (2011).
Readmission Rates for Hispanic Medicare Beneficiaries with Heart
Failure and Acute Myocardial Infarction. Am Heart J., 162(2), 254-
261 e253. Available at: https://www.sciencedirect.com/science/article/pii/S0002870311003966?viewFullText=true. Accessed on
February 14, 2023.
\32\ Centers for Medicare & Medicaid Services. (2014). Medicare
Hospital Quality Chartbook: Performance Report on Outcome Measures.
Available at: https://www.hhs.gov/guidance/sites/default/files/hhs-guidance-documents/YNH_Chartbook_2014_508Compliant_FINAL.pdf.
Accessed on February 14, 2023.
\33\ CMS Office of Minority Health. (2018). Guide to Reducing
Disparities in Readmissions. Available at: https://www.cms.gov/About-CMS/Agency-Information/OMH/Downloads/OMH_Readmissions_Guide.pdf. Accessed on February 14, 2023.
\34\ Prieto-Centurion V, Gussin HA, Rolle AJ, Krishnan JA.
(2013). Chronic Obstructive Pulmonary Disease Readmissions at
Minority Serving Institutions. Ann Am Thorac Soc., 10(6), 680-684.
Available at: https://doi.org/10.1513/AnnalsATS.201307-223OT.
Accessed on February 14, 2023.
\35\ Joynt KE, Orav E, Jha AK. (2011). Thirty-Day Readmission
Rates for Medicare Beneficiaries by Race and Site of Care. JAMA,
305(7), 675-681. Available at: https://jamanetwork.com/journals/jama/fullarticle/645647. Accessed on February 13, 2023.
\36\ Nelson AR. (2003). Unequal Treatment: Report of the
Institute of Medicine on Racial and Ethnic Disparities in
Healthcare. The Annals of Thoracic Surgery, 76(4), S1377-S1381.
https://www.annalsthoracicsurgery.org/action/showPdf?pii=S0003-4975%2803%2901205-0. Accessed on February 14, 2023.
\37\ Peek, ME, Odoms-Young, A, et al. (2010). Race and Shared
Decision-Making: Perspectives of African-Americans with diabetes.
Social Science & Medicine, 71(1), 1-9. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885527/. Accessed on February
14, 2023.
\38\ Department of Health and Human Services. (2023). Healthy
People 2030: Social Determinants of Health. Available at: https://health.gov/healthypeople/priority-areas/social-determinants-health.
Accessed on February 20, 2023.
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Because we are working toward the goal of all patients receiving
high-quality healthcare, regardless of individual characteristics, we
are committed to supporting healthcare organizations in building a
culture of safety and equity that focuses on educating and empowering
their workforce to recognize and eliminate health disparities. This
includes patients receiving the right care, at the right time, in the
right setting for their condition(s), regardless of those
characteristics.
In the FY 2022 IPF PPS final rule (86 FR 42625 through 42632), we
summarized the comments we received in response to our Request for
Information (RFI) on closing health equity gaps in our quality
programs, specifically the IPFQR Program. In response to this RFI,
several commenters recommended that we consider a measure of
organizational commitment to health equity. These commenters further
described how infrastructure supports delivery of equitable care. In
the FY 2023 IPF PPS final rule (87 FR 46865 through 46873), we
described our RFI on overarching principles for measuring equity and
healthcare quality across our quality programs and summarized the
comments we received in response to that RFI. Because we had
specifically solicited comments on the potential for a structural
measure assessing an IPF's commitment to health equity, many commenters
provided input on a structural measure. While many commenters supported
the concept, one commenter expressed concern with this measure concept
and stated that there is no evidence that performance on this measure
will lead to improved patient outcomes (87 FR 46872 through 46873).
However, we believe that strong and committed leadership from IPF
executives and board members is essential and can play a role in
shifting organizational culture and advancing equity goals.
Additionally, studies demonstrate that facility leadership can
positively influence culture for better quality, patient outcomes, and
experience of care.39 40 41 A systematic review of 122
published studies showed that strong leadership that prioritized
safety, quality, and the setting of clear guidance with measurable
goals for improvement resulted in high-performing facilities with
better patient outcomes.\42\ Therefore, we believe leadership
commitment to health equity will have a parallel effect in contributing
to a reduction in health disparities.
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\39\ Bradley EH, Brewster AL, et al. (2018). How Guiding
Coalitions Promote Positive Culture Change in Hospitals: A
Longitudinal Mixed Methods Interventional Study. BMJ Qual Saf.,
27(3), 218-225. Available at: https://qualitysafety.bmj.com/content/qhc/27/3/218.full.pdf. Accessed on February 14, 2023.
\40\ Smith SA, Yount N, Sorra J. (2017). Exploring Relationships
Between Hospital Patient Safety Culture and Consumer Reports Safety
Scores. BMC Health Services Research, 17(1), 143. Available at:
https://bmchealthservres.biomedcentral.com/articles/10.1186/s12913-017-2078-6. Accessed on February 14, 2023.
\41\ Keroack MA, Youngberg BJ, et al. (2007). Organizational
Factors Associated with High Performance in Quality and Safety in
Academic Medical Centers. Acad Med., 82(12), 1178-86. Available at:
https://journals.lww.com/academicmedicine/Fulltext/2007/12000/Organizational_Factors_Associated_with_High.14.aspx. Accessed on
February 14, 2023.
\42\ Millar R, Mannion R, Freeman T, et al. (2013). Hospital
Board Oversight of Quality and Patient Safety: A Narrative Review
and Synthesis of Recent Empirical Research. The Milbank Quarterly,
91(4), 738-70. Available at: https://onlinelibrary.wiley.com/doi/10.1111/1468-0009.12032. Accessed February 14, 2023.
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Further, we note that the Agency for Healthcare Research and
Quality (AHRQ) and The Joint Commission (TJC) identified that facility
leadership plays an important role in promoting a culture of quality
and safety.43 44 45 For instance, AHRQ research shows that a
facility's board can influence quality and safety in a variety of ways,
not only through strategic initiatives, but also through more direct
interactions with frontline workers.\46\
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\43\ Agency for Healthcare Research and Quality. Leadership Role
in Improving Patient Safety. Patient Safety Primer, September 2019.
Available at: https://psnet.ahrq.gov/primer/leadership-role-improving-safety. Accessed on February 14, 2023.
\44\ Joint Commission on Accreditation of Healthcare
Organizations, USA. The essential role of leadership in developing a
safety culture. Sentinel Event Alert. 2017 (Revised June 2021).
Available at: https://www.jointcommission.org/-/media/tjc/documents/resources/patient-safety-topics/sentinel-event/sea-57-safety-culture-and-leadership-final2.pdf. Accessed on February 15, 2023.
\45\ See information on launch of new ``Health Care Equity
Certification'' in July 2023 from Joint Commission on Accreditation
of Healthcare Organizations, USA, available at: https://www.jointcommission.org/our-priorities/health-care-equity/health-care-equity-prepublication/. Accessed on February 15, 2023.
\46\ Agency for Healthcare Research and Quality. Leadership Role
in Improving Patient Safety. Patient Safety Primer. (2019).
Available at: https://psnet.ahrq.gov/primer/leadership-role-improving-safety. Accessed on February 14, 2023.
\47\ Mate KS and Wyatt R. (2017). Health Equity Must Be a
Strategic Priority. NEJM Catalyst. Available at: https://catalyst.nejm.org/doi/full/10.1056/CAT.17.0556. Accessed on February
15, 2023.
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In addition, the Institute of Healthcare Improvement's (IHI's)
research of 23 health systems throughout the United States and Canada
shows that health equity must be a priority championed by leadership
teams to improve both patient access to needed healthcare services and
outcomes among populations that have been disadvantaged by the
healthcare system.\47\ This IHI study specifically identified concrete
actions to make advancing health equity a core strategy,
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including establishing this goal as a leader-driven priority alongside
organizational development structures and processes.\48\
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\48\ Mate KS and Wyatt R. (2017). Health Equity Must Be a
Strategic Priority. NEJM Catalyst. Available at: https://catalyst.nejm.org/doi/full/10.1056/CAT.17.0556. Accessed on February
15, 2023.
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Based upon these findings, we believe that IPF leadership can be
instrumental in setting specific, measurable, attainable, realistic,
and time-based (SMART) goals to assess progress towards achieving
equity goals and ensuring high-quality care is accessible to all.
Therefore, consistent with the Hospital Inpatient Quality Reporting
(IQR) Program's adoption of an attestation-based structural measure in
the FY 2023 IPPS/LTCH PPS final rule (87 FR 49191 through 49201), we
proposed to adopt an attestation-based structural measure, Facility
Commitment to Health Equity, to address health equity beginning with
the CY 2024 reporting period/FY 2026 payment determination.
The first pillar of our strategic priorities \49\ reflects our deep
commitment to improvements in health equity by addressing the health
disparities that underly our health system. In line with this strategic
pillar, we developed this structural measure to assess facility
commitment to health equity across five domains (described in Table 17
in section VI.D.2.b of this final rule) using a suite of organizational
competencies aimed at achieving health equity for racial and ethnic
minority groups, people with disabilities, members of the LGBTQ+
community, individuals with limited English proficiency, rural
populations, religious minorities, and people facing socioeconomic
challenges. We believe these elements are actionable focus areas, and
assessment of IPFs' leadership commitment to them is foundational.
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\49\ Brooks-LaSure, C. (2021). My First 100 Days and Where We Go
From Here: A Strategic Vision for CMS. Centers for Medicare &
Medicaid. Available at: https://www.cms.gov/blog/my-first-100-days-and-where-we-go-here-strategic-vision-cms. Accessed on February 15,
2023. Also see https://www.cms.gov/cms-strategic-plan.
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We also believe adoption of the Facility Commitment to Health
Equity measure will incentivize IPFs to collect and utilize data to
identify critical equity gaps, implement plans to address these gaps,
and ensure that resources are dedicated toward addressing health equity
initiatives. While many factors contribute to health equity, we believe
this measure is an important step toward assessing IPFs' leadership
commitment, and a fundamental step toward closing the gap in equitable
care for all populations. We note that this measure is not intended to
encourage IPFs to act on any one data element or domain, but instead
encourages IPFs to analyze their own findings to understand if there
are any demographic factors (for example, race, national origin,
primary language, and ethnicity) as well as SDOHs (for example, housing
status and food security) associated with underlying inequities and, in
turn, develop solutions to deliver more equitable care. Thus, the
Facility Commitment to Health Equity measure aims to support IPFs in
leveraging available data, pursuing focused quality improvement
activities, and promoting efficient and effective use of resources.
The Facility Commitment to Health Equity measure aligns with the
measure previously adopted in the Hospital IQR Program, and we refer
readers to the FY 2023 IPPS/LTCH PPS final rule (87 FR 49191 through
49201) for more information regarding the measure's adoption in the
Hospital IQR Program. The five domains of the Facility Commitment to
Health Equity measure are adapted from the CMS Office of Minority
Health's Building an Organizational Response to Health Disparities
framework, which focuses on data collection, data analysis, culture of
equity, and quality improvement.\50\
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\50\ CMS. (2021). Building an Organizational Response to Health
Disparities [Fact Sheet]. Available at: https://www.cms.gov/About-CMS/Agency-Information/OMH/Downloads/Health-Disparities-Guide.pdf.
Accessed on February 15, 2023.
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The Facility Commitment to Health Equity measure also aligns with
our efforts under the Meaningful Measures Framework, which identifies
high-priority areas for quality measurement and improvement to assess
core issues most critical to high-quality healthcare and improving
patient outcomes.\51\ In 2021, we launched Meaningful Measures 2.0 to
promote innovation and modernization of all aspects of quality, and to
address a wide variety of settings, stakeholders, and measure
requirements.\52\ We are addressing healthcare priorities and gaps with
Meaningful Measures 2.0 by leveraging quality measures to promote
equity and close gaps in care. The Facility Commitment to Health Equity
measure supports these efforts and is aligned with the Meaningful
Measures Area of ``Equity of Care'' and the Meaningful Measures 2.0
goal to ``Leverage Quality Measures to Promote Equity and Close Gaps in
Care.'' This measure also supports the Meaningful Measures 2.0
objective to commit to a patient-centered approach in quality measure
and value-based incentives programs to ensure that quality and safety
measures address health equity.
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\51\ Centers for Medicare & Medicaid Services. Meaningful
Measures Framework. Available at: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/QualityInitiativesGenInfo/CMS-Quality-Strategy. Accessed on February
15, 2023.
\52\ CMS. (2022). Meaningful Measures 2.0: Moving from Measure
Reduction to Modernization. Available at https://www.cms.gov/medicare/meaningful-measures-framework/meaningful-measures-20-moving-measure-reduction-modernization. Accessed on February 20,
2023.
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b. Overview of Measure
The Facility Commitment to Health Equity measure will assess IPFs'
commitment to health equity using a suite of equity-focused
organizational competencies aimed at achieving health equity for
populations that have been disadvantaged, marginalized, and underserved
by the healthcare system. As previously noted, these populations
include, but are not limited to, racial and ethnic minority groups,
people with disabilities, members of the LGBTQ+ community, individuals
with limited English proficiency, rural populations, religious
minorities, and people facing socioeconomic challenges. Table 17 sets
forth the five attestation domains, and the elements within each of
those domains, to which an IPF will affirmatively attest for the IPF to
receive credit for that domain within the Facility Commitment to Health
Equity measure.
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[GRAPHIC] [TIFF OMITTED] TR02AU23.018
[[Page 51104]]
(1) Measure Calculation
The Facility Commitment to Health Equity measure consists of five
attestation-based questions, each representing a separate domain of the
IPF's commitment to addressing health equity. Some of these domains
have multiple elements to which an IPF will be required to attest. For
an IPF to affirmatively attest ``yes'' to a domain, and receive credit
for that domain, the IPF would evaluate and determine whether it
engages in each of the elements that comprise that domain. Each of the
domains will be represented in the denominator as a point, for a total
of five points (that is, one point per domain).
The numerator of the Facility Commitment to Health Equity measure
will capture the total number of domain attestations that the IPF is
able to affirm. An IPF that affirmatively attests to each element
within the five domains will receive the maximum five points.
An IPF will only receive a point for a domain if it attests ``yes''
to all related elements within that domain. There is no ``partial
credit'' for elements. For example, for Domain 1 (``Facility commitment
to reducing healthcare disparities is strengthened when equity is a key
organizational priority''), an IPF will evaluate and determine whether
its strategic plan meets each of the elements described in (A) through
(D) (see Table 17 in section VI.D.2.b of this final rule). If the IPF's
strategic plan meets all four of these elements, the IPF would
affirmatively attest ``yes'' to Domain 1 and would receive one (1)
point for that attestation. An IPF will not be able to receive partial
credit for a domain. For example, if the IPF's strategic plan meets
elements (A) and (B), but not (C) and (D), of Domain 1, then the IPF
would not be able to affirmatively attest ``yes'' to Domain 1 and would
not receive a point for that attestation, and instead would receive
zero points for Domain 1.
In response to our RFI on the potential for a structural measure
assessing an IPF's commitment to health equity, several commenters
expressed concern that such a measure would be difficult for IPFs to
report because of the requirement to use certified electronic health
record (EHR) technology for Domain 2 (87 FR 46972 through 46873). We
believe that use of certified EHR technology is an important element of
collecting valid and reliable demographic and social drivers of health
data on patients served in an IPF and that use of this technology
facilitates data analytics to ensure consistent, high-quality,
equitable care. However, we recognize that some IPFs may face
challenges to adopting certified EHR technology. We note that the IPFQR
Program is a pay-for-reporting program, not a pay-for-performance
program, and therefore IPFs that do not have certified EHR technology
can attest that they satisfy the other domains, as applicable, and
receive a score of 0-4 out of 5 without any penalties.
(2) Review by the Measure Applications Partnership (MAP) \53\
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\53\ Interested parties convened by the consensus-based entity
provide input and recommendations on the Measures under
Consideration (MUC) list as part of the pre-rulemaking process
required by section 1890A of the Act. We refer readers to https://p4qm.org/PRMR-MSR for more information.
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We included the Facility Commitment to Health Equity measure on the
publicly available MUC List, a list of measures under consideration for
use in various Medicare programs.\54\ The specifications for the
Facility Commitment to Health Equity measure, which were available
during the review of the MUC List, are available on the CMS website at:
https://mmshub.cms.gov/sites/default/files/map-hospital-measure-specifications-manual-2022.pdf.
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\54\ Centers for Medicare & Medicaid Services. List of Measures
Under Consideration for December 1, 2022. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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The CBE-convened MAP Health Equity Advisory Group reviewed the MUC
List and the Facility Commitment to Health Equity measure (MUC 2022-
027) in detail on December 6 through 7, 2022.\55\ The MAP Health Equity
Advisory Group raised concerns that this measure does not evaluate
outcomes and may not directly address health inequities at a systemic
level, but generally agreed that a structural measure such as this one
represents progress toward improving equitable care.\56\
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\55\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\56\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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In addition, on December 8 through 9, 2022, the MAP Rural Health
Advisory Group reviewed the 2022 MUC List and expressed support for
this measure as a step towards advancing access to and quality of care
with the caveat that resource challenges exist in rural
communities.\57\
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\57\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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The MAP Hospital Workgroup reviewed the 2022 MUC List on December
13 through 14, 2022.\58\ The MAP Hospital Workgroup recognized that
reducing health care disparities would represent a substantial benefit
to overall quality of care but expressed reservations about the
measure's link to clinical outcomes. As stated in the MAP
recommendations document, the MAP Hospital Workgroup members voted to
conditionally support the Facility Commitment to Health Equity measure
for rulemaking pending: (1) endorsement by the CBE; (2) commitment to
consideration of equity related outcome measures in the future; (3)
provision of more clarity on the Facility Commitment to Health Equity
measure and supplementing interpretation with results; and (4)
verification of accurate attestation by IPFs.\59\ Thereafter, the MAP
Coordinating Committee deliberated on January 24 through 25, 2023 and
ultimately voted to uphold the MAP Hospital Workgroup's recommendation
to conditionally support the measure for rulemaking.\60\
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\58\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\59\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\60\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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We believe that the Facility Commitment to Health Equity measure
establishes an important foundation for prioritizing the achievement of
health equity among IPFs participating in the IPFQR Program. Our
approach to developing health equity measures has been incremental to
date, but we see inclusion of such measures in the IPFQR Program as
informing efforts to advance and achieve health equity not only among
IPFs, but also other acute care settings. We believe this measure to be
a building block that lays the groundwork for a future meaningful suite
of measures that would assess IPF progress in providing high-quality
healthcare for all patients regardless of social risk factors or
demographic characteristics.
(3) CBE Endorsement
We have not submitted this measure for CBE endorsement at this
time.
[[Page 51105]]
Although section 1886(s)(4)(D)(i) of the Act generally requires that
measures specified by the Secretary must be endorsed by the entity with
a contract under section 1890(a) of the Act, section 1886(s)(4)(D)(ii)
of the Act states that, in the case of a specified area or medical
topic determined appropriate by the Secretary for which a feasible and
practical measure has not been endorsed by the entity with a contract
under section 1890(a) of the Act, the Secretary may specify a measure
that is not so endorsed as long as due consideration is given to
measures that have been endorsed or adopted by a consensus organization
identified by the Secretary. We reviewed measures endorsed by consensus
organizations and were unable to identify any other measures on this
topic endorsed by a consensus organization, and therefore, we believe
the exception in section 1886(s)(4)(D)(ii) of the Act applies.
c. Data Collection, Submission, and Reporting
IPFs are required to submit information for structural measures
once annually using a CMS-approved web-based data collection tool
available within the Hospital Quality Reporting (HQR) System. For more
information about our previously finalized policies related to
reporting of structural measures, we refer readers to the FY 2014 IPPS/
LTCH PPS final rule (78 FR 50890 through 50901) and the FY 2015 IPF PPS
final rule (79 FR 45963 through 45964 and 45976). Given the role of
committed leadership in improving health outcomes for all patients, we
proposed to adopt this measure beginning with attestations submitted to
CMS in CY 2025 reflecting the CY 2024 reporting period and affecting
the FY 2026 payment determination.
We invited comments on our proposed adoption of the Facility
Commitment to Health Equity Measure beginning with the FY 2026 payment
determination.
Comment: Many commenters supported adoption of the Facility
Commitment to Health Equity measure. One commenter stated that
alignment with other programs will support consistent measurement
across the continuum of patient care. Several commenters stated that
facilities' commitment to health equity is particularly important for
IPFs because of health disparities experienced by patients with mental
health conditions. Several commenters stated that the Facility
Commitment to Health Equity measure is consistent with new standards
from The Joint Commission. One commenter stated that facilities
attesting to their commitment to health equity will help empower the
healthcare workforce to recognize and eliminate health disparities.
Response: We thank commenters for their support of our proposal to
adopt the Facility Commitment to Health Equity measure and agree that
this measure addresses a topic that is important for IPF patients and
this setting.
Comment: Other commenters recommended additional testing,
specifically in the IPF setting, to ensure that this measure addresses
unique challenges associated with treating the psychiatric patient
population prior to adoption of this measure. Some of these commenters
also recommended engaging IPFs to voluntarily test the measure to
ensure usability, acceptability, and face validity are met for this
setting.
Response: We acknowledge that this measure was initially developed
for the general acute care setting. While we recognize the value of
measures undergoing testing and evaluation of validity and feasibility
in the setting for which they are being adopted, given the urgency of
achieving health equity and, as there are currently no other existing
measures that address facility commitment to health equity, we believe
it is important to implement this measure as soon as feasible. Strong
and consistent facility leadership can be instrumental in establishing
specific, measurable, and attainable goals to advance equity priorities
and improve care for all patients in any care setting, including
patients who receive care in inpatient psychiatric facilities. We
believe that this measure is equally applicable to freestanding IPFs
and psychiatric units within acute care facilities as it is to general
acute care settings. Leaders of health services organizations across
the health care system, including both IPFs and acute care hospitals,
are likely to encounter the same challenges and use the same types of
strategies to achieve organizational goals related to improving health
equity within their respective organizations. We note that health
equity is a critical topic for patients treated in IPFs and that there
are high levels of health disparities experienced by this patient
population. CMS will monitor measure implementation and data reporting
as part of standard program and measure review and will consider
updates to the measure if improvements are identified through this
process.
Comment: Many commenters expressed concern that this measure has
not received endorsement by the CBE.
Response: While we recognize the value of measures undergoing
review for potential CBE endorsement, given the urgency of achieving
health equity, we believe it is important to implement this measure
beginning with the CY 2024 reporting period. We note that, in
accordance with section 1886(s)(4)(D)(ii) of the Act, the Secretary may
specify a measure that is not so endorsed as long as due consideration
is given to measures that have been endorsed or adopted by a consensus
organization identified by the Secretary. We reviewed measures endorsed
by consensus organizations and were unable to identify any other
measures on this topic endorsed by a consensus organization, and
therefore, we believe the exception in section 1886(s)(4)(D)(ii) of the
Act applies.
Comment: Some commenters recommended that CMS defer adoption of
this measure until CMS and IPFs have reviewed the Hospital IQR
Program's implementation of this measure to identify potential
improvements to data collection processes that would reduce burden for
IPFs. These commenters stated that IPFs often have fewer resources
available for data collection relative to acute care hospitals.
Response: We acknowledge commenters' desire to be able to learn
from the experiences of acute care hospitals reporting this measure. We
note that hospitals participating in the Hospital IQR Program will have
already reported data on the similar Hospital Commitment to Health
Equity measure for the FY 2025 payment determination (that is, data
submitted in CY 2024 representing the CY 2023 performance period) (87
FR 49201) before the reporting of the Facility Commitment to Health
Equity Measure for the IPFQR Program begins with the FY 2026 payment
determination. Given the timing of this similar measure in the Hospital
IQR Program, we believe IPFs will have had the opportunity to learn
from the experiences of acute care hospitals, including best practices
for minimally burdensome assessment of performance on the required
domains.
Comment: Many commenters supported adoption of this measure on the
condition that CMS commit to development and adoption of health equity
related outcome measures in the future.
Response: We believe this measure to be a building block that lays
the groundwork for a more comprehensive suite of measures that would
assess progress in providing high-quality healthcare for all patients
regardless of social risk factors or demographic
[[Page 51106]]
characteristics. This more comprehensive suite of measures could
eventually include health equity related outcome measures.
Comment: Many commenters recommended that CMS establish a process
to ensure that results are publicly reported in a way that helps
patients interpret IPF scores on the Facility Commitment to Health
Equity measure.
Response: We believe this measure will provide insightful
information to healthcare providers and the public on the number of
IPFs currently participating in health equity strategic planning,
collecting data, using these data to identify equity gaps, establishing
key performance indicators, and reviewing them with hospital senior
leaders. We intend to provide educational materials as part of our
outreach and public reporting of this measure to ensure understanding
and interpretation of publicly reported data.
Comment: Many commenters recommended that prior to adoption of the
Facility Commitment to Health Equity measure CMS identify a means to
verify accurate attestation of commitment by IPFs.
Response: We understand commenters' concerns regarding the accuracy
of provider self-reported data. While we do not have a specific means
to validate IPFs' attestation to this measure, we do require all IPFs
participating in the IPFQR Program to complete the Data Accuracy and
Completeness Acknowledgement (DACA) each year, which requires
attestation that all of the information reported to CMS for the IPFQR
Program is accurate and complete. For more information on the IPFQR
Program's DACA requirements, we refer readers to the FY 2013 IPPS/LTCH
PPS final rule (77 FR 53658).
Comment: Several commenters recommended that CMS update the measure
specifications so that IPFs without certified EHR technology are able
to positively attest to all domains. These commenters expressed concern
that public reporting of measure results for IPFs that do not
positively attest to all domains because they are without access to
certified EHR technology could lead the public to misinterpret the
results as a lack of commitment to health equity when it is actually a
resource limitation which, the commenters believed, is due to a lack of
federal funding for EHR implementation.
Response: We acknowledge that some IPFs may face challenges to
adopting certified EHR technology. We note that the IPFQR Program is a
pay-for-reporting program, not a pay-for-performance program, and
therefore IPFs that do not have certified EHR technology can attest
that they satisfy the other domains, as applicable, and receive a score
of 0-4 out of 5 without any penalties. We understand the commenters'
concern that the public may misinterpret IPFs' reported results that
are due to resource limitations as a lack of commitment to health
equity. To reduce the likelihood of misinterpretation, we intend to
provide educational materials as part of our outreach and public
reporting of this measure to ensure understanding and appropriate
interpretation of publicly reported data.
Comment: Some commenters recommended respecifying the measure so
that IPFs are scored on a zero to eleven scale (one point for each
element within a domain) as opposed to a zero to five scale (one point
for each domain). Other commenters recommended only requiring
attestation for 3 out of 5 domains. Some of these commenters stated
that some domains are harder to achieve or have more required elements
for attestation than others and expressed the belief that reducing the
number of required domains would address this concern.
Response: We believe the five domains of this measure are
actionable focus areas, and assessment of facility leadership
commitment to them is foundational. We also believe this measure will
incentivize providers to collect and utilize data to identify critical
equity gaps, implement plans to address any identified gaps, and ensure
that resources are dedicated toward addressing health equity
initiatives. The five questions of the proposed structural measure are
adapted from the CMS Office of Minority Health's Building an
Organizational Response to Health Disparities framework, which focuses
on data collection, data analysis, culture of equity, and quality
improvement.\61\ We believe that accomplishing each element within a
domain is important together with the other elements to help hospitals
identify, prioritize, and take action on health disparities.
Additionally, as discussed previously, we note that the IPFQR Program
is a pay-for-reporting program, and IPFs are not scored based on their
performance on measures.
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\61\ Centers for Medicare & Medicaid Services. (2021). Building
an Organizational Response to Health Disparities [Fact Sheet]. U.S.
Department of Health and Human Services. Available at: https://www.cms.gov/About-CMS/Agency-Information/OMH/Downloads/Health-Disparities-Guide.pdf.
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Comment: Several commenters expressed concern that IPFs may not
report the measure consistently, and one commenter recommended that CMS
provide clarification of key terms (such as ``strategic plan'') to
mitigate the risk of inconsistent reporting.
Response: We note that Attestation Guidance for the similar measure
adopted in the Hospital IQR Program (the Hospital Commitment to Health
Equity measure), includes definitions of key terms including
``strategic plan,'' which we define as ``a written plan to address
health equity that is shared across the hospital'' (or facility in the
case of IPFs).\62\ To help with consistent implementation, we will
develop a similar Attestation Guidance document for IPFs as part of
providing educational and training materials, and which will be
conveyed through routine communication channels to IPFs, vendors, and
QIOs, including, but not limited to, issuing memos, emails, and notices
on a CMS website.
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\62\ Available at: https://qualitynet.cms.gov/files/6481de126f7752001c37e34f?filename=AttstGdnceHCHEMeas_v1.1.pdf.
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Comment: One commenter did not support adoption of the Facility
Commitment to Health Equity measure and expressed their belief that
there is insufficient evidence that this measure leads to improved
patient outcomes.
Response: We believe this measure is an important foundational
measure for improving health equity among those that have been
disadvantaged or underserved by the healthcare system. Furthermore, as
discussed in section VI.D.2.a of the proposed rule, there is
substantial research showing differences in care and experiences among
these populations (88 FR 21274 through 21275). We also believe adoption
of the Facility Commitment to Health Equity measure will incentivize
IPFs to collect and utilize data to identify critical equity gaps,
implement plans to address these gaps, and ensure that resources are
dedicated toward addressing health equity initiatives. This measure
aims to support IPFs in leveraging available data, pursuing focused
quality improvement activities, and promoting efficient and effective
use of resources. Through this measure, providers are encouraged to
analyze their own data to understand the many factors, including race,
ethnicity, and various social drivers of health, such as housing
stability and food security, in order to deliver more equitable care.
We believe the delivery of more equitable care will, in turn, improve
patient outcomes.
[[Page 51107]]
Final Decision: After consideration of the public comments we
received, we are finalizing adoption of the Facility Commitment to
Health Equity measure as proposed.
3. Adoption of the Screening for Social Drivers of Health Measure
Beginning With Voluntary Reporting of CY 2024 Data Followed by
Mandatory Reporting Beginning With CY 2025 Data/FY 2027 Payment
Determination
a. Background
Health-related social needs (HRSNs), which we define as individual-
level, adverse social conditions that negatively impact an individual
person's health or healthcare, are significant risk factors associated
with worse health outcomes as well as increased healthcare
utilization.\63\ We believe that consistently pursuing identification
of HRSNs would have two significant benefits. First, HRSNs
disproportionately impact people who have historically been underserved
by the healthcare system,\64\ and screening helps identify individuals
who may have HRSNs. Second, screening for HRSNs could support ongoing
IPF quality improvement initiatives by providing data with which to
stratify patient risk and organizational performance. Further, we
believe that IPFs collecting patient-level HRSN data through screening
is essential for the long-term in encouraging meaningful collaboration
between healthcare providers and community-based organizations and in
implementing and evaluating related innovations in health and social
care delivery.
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\63\ Centers for Medicare & Medicaid Services. (2021). A Guide
to Using the Accountable Health Communities Health-Related Social
Needs Screening Tool: Promising Practices and Key Insights. June
2021. Available at: https://innovation.cms.gov/media/document/ahcm-screeningtool-companion. Accessed on February 20, 2023.
\64\ American Hospital Association. (2020). Health Equity,
Diversity & Inclusion Measures for Hospitals and Health System
Dashboards. December 2020. Available at: https://ifdhe.aha.org/system/files/media/file/2020/12/ifdhe_inclusion_dashboard.pdf.
Accessed on February 20, 2023.
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Health disparities manifest primarily as worse health outcomes in
population groups where access to care is
inequitable.65 66 67 68 69 Such differences persist across
geography and healthcare settings irrespective of improvements in
quality of care over time.70 71 72 Assessment of HRSNs is an
essential mechanism for capturing the interaction between social,
community, and environmental factors associated with health status and
health outcomes.73 74 75
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\65\ Seligman, H.K., & Berkowitz, S.A. (2019). Aligning Programs
and Policies to Support Food Security and Public Health Goals in the
United States. Annual Review of Public Health, 40(1), 319-337.
Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784838/.
Accessed on February 20, 2023.
\66\ The Physicians Foundation. (2020). Survey of America's
Patients, Part Three. Available at: https://physiciansfoundation.org/wp-content/uploads/2020/10/2020-Physicians-Foundation-Survey-Part3.pdf. Accessed on February 20, 2023.
\67\ Office of the Assistant Secretary for Planning and
Evaluation (ASPE) (2020). Report to Congress: Social Risk Factors
and Performance Under Medicare's Value-Based Purchasing Program
(Second of Two Reports). Available at: https://aspe.hhs.gov/pdf-report/second-impact-report-to-congress. Accessed on February 20,
2023.
\68\ Trivedi AN, Nsa W, Hausmann LRM, et al. (2014). Quality and
Equity of Care in U.S. Hospitals. N Engl J Med, 371(24), 2298-2308.
Available at: https://www.nejm.org/doi/10.1056/NEJMsa1405003.
Accessed on February 13, 2023.
\69\ Billioux, A., Verlander, K., Anthony, S., & Alley, D.
(2017). Standardized Screening for Health Related Social Needs in
Clinical Settings: The Accountable Health Communities Screening
Tool. NAM Perspectives, 7(5). Available at: https://doi.org/10.31478/201705b. Accessed on February 20, 2023.
\70\ Office of the Assistant Secretary for Planning and
Evaluation (ASPE) (2020). Report to Congress: Social Risk Factors
and Performance Under Medicare's Value-Based Purchasing Program
(Second of Two Reports). Available at: https://aspe.hhs.gov/pdf-report/second-impact-report-to-congress. Accessed on February 20,
2023.>
\71\ Hill-Briggs, F. (2021). Social Determinants of Health and
Diabetes: A Scientific Review. Diabetes Care. Available at: https://diabetesjournals.org/care/article/44/1/258/33180/Social-Determinants-of-Health-and-Diabetes-A. Accessed on February 20,
2023.
\72\ Khullar, D., MD. (2020). Association Between Patient Social
Risk and Physician Performance American academy of Family
Physicians. Addressing Social Determinants of Health in Primary Care
team-based approach for advancing health equity. Available at:
https://www.aafp.org/dam/AAFP/documents/patient_care/everyone_project/team-based-approach.pdf. Accessed on February 20,
2023.
\73\ Institute of Medicine. (2014). Capturing Social and
Behavioral Domains and Measures in Electronic Health Records: Phase
2. Washington, DC: The National Academies Press. Available at:
https://doi.org/10.17226/18951. Accessed on February 20, 2023.
\74\ Alley, D.E., C.N. Asomugha, P.H. Conway, and D.M. Sanghavi.
(2016). Accountable Health Communities--Addressing Social Needs
through Medicare and Medicaid. The New England Journal of Medicine
374(1):8-11. Available at: https://doi.org/10.1056/NEJMp1512532.
Accessed on February 20, 2023.
\75\ Centers for Disease Control and Prevention. CDC COVID-19
Response Health Equity Strategy: Accelerating Progress Towards
Reducing COVID-19 Disparities and Achieving Health Equity. July
2020. Available at: https://www.cdc.gov/coronavirus/2019-ncov/community/health-equity/cdc-strategy.html. Accessed on February 2,
2023.
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Growing evidence demonstrates that specific HRSNs are directly
associated with patient health outcomes as well as healthcare
utilization, costs, and performance in quality-based payment
programs.76 77 While widespread interest in addressing HRSNs
exists, action is inconsistent.\78\
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\76\ Zhang Y, Li J, Yu J, Braun RT, Casalino LP (2021). Social
Determinants of Health and Geographic Variation in Medicare per
Beneficiary Spending. JAMA Network Open. 2021;4(6):e2113212. https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2780864.
Accessed on February 20, 2023.
\77\ Khullar, D., Schpero, W.L., Bond, A.M., Qian, Y., &
Casalino, L.P. (2020). Association Between Patient Social Risk and
Physician Performance Scores in the First Year of the Merit-based
Incentive Payment System. JAMA, 324(10), 975-983. https://doi.org/10.1001/jama.2020.13129. Accessed on February 20, 2023.
\78\ TK Fraze, AL Brewster, VA Lewis, LB Beidler, GF Murray, CH
Colla. Prevalence of screening for food insecurity, housing
instability, utility needs, transportation needs, and interpersonal
violence by US physician practices and hospitals. JAMA Network Open
2019; https://jamanetwork.com/journals/jamanetworkopen/fullarticle/10.1001/jamanetworkopen.2019.11514. Accessed on February 20, 2023.
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While social risk factors account for 50 to 70 percent of health
outcomes, the mechanisms by which this connection emerges are complex
and multifaceted.79 80 81 82 The persistent interactions
among individuals' HRSNs, medical providers' practices and behaviors,
and community resources significantly impact healthcare access,
quality, and ultimately costs, as described in the CMS Equity Plan for
Improving Quality in Medicare.83 84 In their 2018 survey, to
which more than 8,500 physicians responded, the
[[Page 51108]]
Physicians Foundation found that almost 90 percent of these physician
respondents reported their patients had a serious health problem linked
to poverty or other social conditions.\85\ Additionally, associations
among disproportionate health risk, hospitalization, and adverse health
outcomes have been highlighted and magnified by the COVID-19
pandemic.86 87
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\79\ Kaiser Family Foundation. (2021). Racial and Ethnic Health
Inequities and Medicare. Available at: https://www.kff.org/medicare/report/racial-and-ethnic-health-inequities-and-medicare/. Accessed
February 20, 2023.
\80\ Khullar, D., MD. (2020). Association Between Patient Social
Risk and Physician Performance American academy of Family
Physicians. Addressing Social Determinants of Health in Primary Care
team-based approach for advancing health equity. Available at:
https://www.aafp.org/dam/AAFP/documents/patient_care/everyone_project/team-based-approach.pdf. Accessed on February 20,
2023.
\81\ Hammond, G., Johnston, K., Huang, K., Joynt Maddox, K.
(2020). Social Determinants of Health Improve Predictive Accuracy of
Clinical Risk Models for Cardiovascular Hospitalization, Annual
Cost, and Death. Circulation: Cardiovascular Quality and Outcomes,
13 (6) 290-299. Available at: https://doi.org/10.1161/CIRCOUTCOMES.120.006752. Accessed on February 20, 2023.
\82\ The Physicians Foundation. (2021). Viewpoints: Social
Determinants of Health. Available at: https://physiciansfoundation.org/wp-content/uploads/2019/08/The-Physicians-Foundation-SDOH-Viewpoints.pdf. Accessed on February 20, 2023.
\83\ Centers for Medicare & Medicaid Services. (2021). Paving
the Way to Equity: A Progress Report. Available at: https://www.cms.gov/files/document/paving-way-equity-cms-omh-progress-report.pdf. Accessed on February 20, 2023.
\84\ Centers for Medicare & Medicaid Services Office of Minority
Health. (2021). The CMS Equity Plan for Improving Quality in
Medicare. 2015-2021. Available at: https://www.cms.gov/About-CMS/
Agency-Information/OMH/OMH_Dwnld-
CMS_EquityPlanforMedicare_090615.pdf#:~:text=The%20Centers%20for%20Me
dicare%20%26%20Medicaid%20Services%20%28CMS%29,evidence%20base%2C%20i
dentifying%20opportunities%2C%20and%20gathering%20stakeholder%20input
. Accessed on February 20, 2023.
\85\ The Physicians Foundation. (2019). Viewpoints: Social
Determinants of Health. Available at: https://physiciansfoundation.org/wp-content/uploads/2019/08/The-Physicians-Foundation-SDOH-Viewpoints.pdf. Accessed on February 20, 2023.
\86\ Centers for Disease Control and Prevention. (2020). CDC
COVID-19 Response Health Equity Strategy: Accelerating Progress
Towards Reducing COVID-19 Disparities and Achieving Health Equity.
July 2020. Available at: https://www.cdc.gov/coronavirus/2019-ncov/community/health-equity/cdc-strategy.html. Accessed on February 20,
2023.
\87\ Kaiser Family Foundation. (2021). Racial and Ethnic Health
Inequities and Medicare. Available at: https://www.kff.org/medicare/report/racial-and-ethnic-health-inequities-and-medicare/. Accessed
on February 20, 2023.
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In 2017, CMS' Center for Medicare and Medicaid Innovation (CMMI)
launched the Accountable Health Communities (AHC) Model to test the
impact of systematically identifying and addressing the HRSNs of
Medicare and Medicaid beneficiaries (that is, through screening,
referral, and community navigation) on their health outcomes and
related healthcare utilization and costs.\88\ \89\ \90\ \91\ The AHC
Model is one of the first federal pilots to systematically test whether
identifying and addressing core HRSNs improves healthcare costs,
utilization, and outcomes with over 600 clinical sites in 21
states.\92\ The AHC Model had a 5-year period of performance that began
in May 2017 and ended in April 2022, with beneficiary screening
beginning in the summer of 2018.\93\ \94\ Evaluation of the AHC Model
data is still underway.
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\88\ Centers for Medicare & Medicaid Services. (2021). A Guide
to Using the Accountable Health Communities Health-Related Social
Needs Screening Tool: Promising Practices and Key Insights. June
2021. Accessed: November 23, 2021. Available at: https://innovation.cms.gov/media/document/ahcm-screeningtool-companion.
Accessed on February 20, 2023.
\89\ Alley, D.E., Asomugha, C.N., et al. (2016). Accountable
Health Communities--Addressing Social Needs through Medicare and
Medicaid. The New England Journal of Medicine 374(1):8-11. Available
at: https://doi.org/10.1056/NEJMp1512532. Accessed on February 20,
2023.
\90\ Billioux, A., Verlander, K., Anthony, S., & Alley, D.
(2017). Standardized Screening for Health-Related Social Needs in
Clinical Settings: The Accountable Health Communities Screening
Tool. NAM Perspectives, 7(5). Available at: https://doi.org/10.31478/201705b. Accessed on February 20, 2023.
\91\ Centers for Medicare & Medicaid Services. (2021).
Accountable Health Communities Model. Accountable Health Communities
Model [verbar] CMS Innovation Center Available at: https://innovation.cms.gov/innovation-models/ahcm. Accessed on February 20,
2023.
\92\ RTI International. (2020). Accountable Health Communities
(AHC) Model Evaluation. Available at: https://innovation.cms.gov/data-and-reports/2020/ahc-first-eval-rpt. Accessed on February 20,
2023.
\93\ RTI International. (2020). Accountable Health Communities
(AHC) Model Evaluation. Available at: https://innovation.cms.gov/data-and-reports/2020/ahc-first-eval-rpt. Accessed on February 20,
2023.
\94\ We note that the model officially concluded in April 2022,
but many awardees have continued with no-cost extensions to continue
utilizing unspent cooperative agreement funding and all awardees
will conclude by April 2023.
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Under the AHC Model, the following five core domains were selected
to screen for HRSNs among Medicare and Medicaid beneficiaries: (1) food
insecurity; (2) housing instability; (3) transportation needs; (4)
utility difficulties; and (5) interpersonal safety. These domains were
chosen based upon literature review and expert consensus utilizing the
following criteria: (1) availability of high-quality scientific
evidence linking a given HRSN to adverse health outcomes and increased
healthcare utilization, including hospitalizations and associated
costs; (2) ability for a given HRSN to be screened and identified in
the inpatient setting prior to discharge, addressed by community-based
services, and potentially improve healthcare outcomes, including
reduced readmissions; and (3) evidence that a given HRSN is not
systematically addressed by healthcare providers.\95\ In addition to
established evidence of their association with health status, risk, and
outcomes, these five domains were selected because they can be assessed
across the broadest spectrum of individuals in a variety of
settings.96 97 98
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\95\ Billioux, A., Verlander, K., Anthony, S., & Alley, D.
(2017). Standardized Screening for Health-Related Social Needs in
Clinical Settings: The Accountable Health Communities Screening
Tool. NAM Perspectives, 7(5). Available at: https://doi.org/10.31478/201705b. Accessed on February 20, 2023.
\96\ Billioux, A., Verlander, K., Anthony, S., & Alley, D.
(2017). Standardized Screening for Health-Related Social Needs in
Clinical Settings: The Accountable Health Communities Screening
Tool. NAM Perspectives, 7(5). Available at: https://doi.org/10.31478/201705b. Accessed on February 20, 2023.
\97\ Centers for Medicare & Medicaid Services. (2021).
Accountable Health Communities Model. Accountable Health Communities
Model CMS Innovation Center. Available at: https://innovation.cms.gov/innovation-models/ahcm. Accessed on February 20,
2023.
\98\ Kamyck, D., Senior Director of Marketing. (2019). CMS
releases standardized screening tool for health-related social
needs. Activate Care. Available at: https://blog.activatecare.com/standardized-screening-for-health-related-social-needs-in-clinical-settings-the-accountable-health-communities-screening-tool/.
Accessed on February 20, 2023.
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These five evidence-based HRSN domains, which informed development
of the two Social Drivers of Health measures adopted in the Hospital
IQR Program and finalized here for the IPFQR Program, are described in
Table 18. We note that while the measures were initially developed by
The Health Initiative (THI), CMS has since assumed stewardship.
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\99\ Berkowitz SA, Seligman HK, Meigs JB, Basu S. Food
insecurity, healthcare utilization, and high cost: a longitudinal
cohort study. Am J Managed Care. 2018 Sep;24(9):399-404. PMID:
30222918; PMCID: PMC6426124. Available at https://pubmed.ncbi.nlm.nih.gov/30222918/. Accessed on February 20, 2023.
\100\ Hill-Briggs, F. (2021). Social Determinants of Health and
Diabetes: A Scientific Review. Diabetes Care. Available at: https://diabetesjournals.org/care/article/44/1/258/33180/Social-Determinants-of-Health-and-Diabetes-A. Accessed on February 20,
2023.
\101\ Seligman, H.K., & Berkowitz, S.A. (2019). Aligning
Programs and Policies to Support Food Security and Public Health
Goals in the United States. Annual Review of Public Health, 40(1),
319-337. Available at: https://pubmed.ncbi.nlm.nih.gov/30444684/.
Accessed on February 20, 2023.
\102\ National Academies of Sciences, Engineering, and Medicine
2006. Executive Summary: Cost-Benefit Analysis of Providing Non-
Emergency Medical Transportation. Washington, DC: The National
Academies Press. Available at: https://doi.org/10.17226/23285.
Accessed on February 20, 2023.
\103\ Hill-Briggs, F. (2021). Social Determinants of Health and
Diabetes: A Scientific Review. Diabetes Care. Available at: https://diabetesjournals.org/care/article/44/1/258/33180/Social-Determinants-of-Health-and-Diabetes-A. Accessed on February 20,
2023.
\104\ Berkowitz SA, Seligman HK, Meigs JB, Basu S. Food
insecurity, healthcare utilization, and high cost: a longitudinal
cohort study. Am J Managed Care. 2018 Sep;24(9):399-404. PMID:
30222918; PMCID: PMC6426124. Available at https://pubmed.ncbi.nlm.nih.gov/30222918/. Accessed on February 20, 2023.
\105\ Dean, E.B., French, M.T., & Mortensen, K. (2020a). Food
insecurity, health care utilization, and health care expenditures.
Health Services Research, 55(S2), 883-893. Available at: https://doi.org/10.1111/1475-6773.13283. Accessed on February 20, 2023.
\106\ https://ps.psychiatryonline.org/doi/10.1176/appi.ps.201300022?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%20%200pubmed.
Accessed on February 20, 2023.
\107\ Larimer, M.E. (2009). Health Care and Public Service Use
and Costs Before and After Provision of Housing for Chronically
Homeless Persons with Severe Alcohol Problems. JAMA, 301(13), 1349.
Available at: https://doi.org/10.1001/jama.2009.414.
\108\ Hill-Briggs, F. (2021, January 1). Social Determinants of
Health and Diabetes: A Scientific Review. Diabetes Care. Available
at: https://pubmed.ncbi.nlm.nih.gov/33139407/.
\109\ Henry, M., de Sousa, T., Roddey, C., Gayen, S., Bednar,
T.; Abt Associates. The 2020 Annual Homeless Assessment Report
(AHAR) to Congress; Part 1: Point-in-Time Estimates of Homelessness,
January 2021. U.S. Department of Housing and Urban Development.
Accessed November 24, 2021. Available at: https://www.huduser.gov/portal/sites/default/files/pdf/2020-AHAR-Part-1.pdf.
\110\ Larimer, M.E. (2009). Health Care and Public Service Use
and Costs Before and After Provision of Housing for Chronically
Homeless Persons with Severe Alcohol Problems. JAMA, 301(13), 1349.
Available at: https://doi.org/10.1001/jama.2009.414.
\111\ Baxter, A., Tweed, E., Katikireddi, S., Thomson, H.
(2019). Effects of Housing First approaches on health and well-being
of adults who are homeless or at risk of homelessness: systematic
review and meta-analysis of randomized controlled trials. Journal of
Epidemiology and Community Health, 73; 379-387. Available at:
https://jech.bmj.com/content/jech/73/5/379.full.pdf.
\112\ Housing Instability and Mental Health. UNC Greensboro. May
7, 2021. Available at: https://chcs.uncg.edu/housing-instability-
mental-health/
#:~:text=Mental%20health%20is%20correlated%20with%20housing%20in%20se
veral,homeless%20population%20in%20America%20suffer%20a%20mental%20il
lness. Accessed on December 7, 2022.
\113\ National Academies of Sciences, Engineering, and Medicine
2006. Executive Summary: Cost-Benefit Analysis of Providing Non-
Emergency Medical Transportation. Washington, DC: The National
Academies Press. Available at: https://doi.org/10.17226/23285.
\114\ National Academies of Sciences, Engineering, and Medicine
2006. Executive Summary: Cost-Benefit Analysis of Providing Non-
Emergency Medical Transportation. Washington, DC: The National
Academies Press. Available at: https://doi.org/10.17226/23285.
\115\ Hill-Briggs, F. (2021, January 1). Social Determinants of
Health and Diabetes: A Scientific Review. Diabetes Care. Available
at: https://pubmed.ncbi.nlm.nih.gov/33139407/.
\116\ Billioux, A., Verlander, K., Anthony, S., & Alley, D.
(2017). Standardized Screening for Health-Related Social Needs in
Clinical Settings: The Accountable Health Communities Screening
Tool. NAM Perspectives, 7(5). Available at: https://doi.org/10.31478/201705b.
\117\ Shier, G., Ginsburg, M., Howell, J., Volland, P., &
Golden, R. (2013). Strong Social Support Services, Such as
Transportation And Help For Caregivers, Can Lead To Lower Health
Care Use And Costs. Health Affairs, 32(3), 544-551. Available at:
https://doi.org/10.1377/hlthaff.2012.0170.
\118\ https://www.nami.org/Advocacy/Policy-Priorities/Supporting-Community-Inclusion-and-Non-Discrimination/Medicaid-Non-Emergency-Medical-Transportation.
\119\ Baxter, A., Tweed, E., Katikireddi, S., Thomson, H.
(2019). Effects of Housing First approaches on health and well-being
of adults who are homeless or at risk of homelessness: systematic
review and meta-analysis of randomized controlled trials. Journal of
Epidemiology and Community Health, 73; 379-387. Available at:
https://jech.bmj.com/content/jech/73/5/379.full.pdf.
\120\ Wright, B.J., Vartanian, K.B., Li, H.F., Royal, N., &
Matson, J.K. (2016). Formerly Homeless People Had Lower Overall
Health Care Expenditures After Moving into Supportive Housing.
Health Affairs, 35(1), 20-27. Available at: https://doi.org/10.1377/hlthaff.2015.0393.
\121\ Billioux, A., Verlander, K., Anthony, S., & Alley, D.
(2017). Standardized Screening for Health-Related Social Needs in
Clinical Settings: The Accountable Health Communities Screening
Tool. NAM Perspectives, 7(5). Available at: https://doi.org/10.31478/201705b.
\122\ Henry M., de Sousa, T., Roddey, C., Gayen, S., Bednar, T.;
Abt Associates. The 2020 Annual Homeless Assessment Report (AHAR) to
Congress; Part 1: Point-in-Time Estimates of Homelessness, January
2021. U.S. Department of Housing and Urban Development. Accessed
November 24, 2021. Available at: https://www.huduser.gov/portal/sites/default/files/pdf/2020-AHAR-Part-1.pdf.
\123\ Larimer, M.E. (2009). Health Care and Public Service Use
and Costs Before and After Provision of Housing for Chronically
Homeless Persons with Severe Alcohol Problems. JAMA, 301(13), 1349.
Available at: https://doi.org/10.1001/jama.2009.414.
\124\ https://ajph.aphapublications.org/doi/abs/10.2105/AJPH.2013.301680.
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As a first step towards leveraging the opportunity to close equity
gaps by identifying patients' HRSNs, we finalized the adoption of two
evidence-based measures in the Hospital IQR Program--the Screening for
Social Drivers of Health measure and the Screen Positive Rate for
Social Drivers of Health measure (collectively, Social Drivers of
Health measures)--and refer readers to the FY 2023 IPPS/LTCH PPS final
rule (87 FR 49191 through 49220).
Through adoption in the IPFQR Program, these two Social Drivers of
Health measures (that is, the Screening for Social Drivers of Health
measure discussed in this section and the Screen Positive Rate for
Social Drivers of Health measure discussed in section VI.D.4 of this
final rule) will support identification of specific risk factors for
inadequate healthcare access and adverse health outcomes among
patients. We note that these measures will enable systematic collection
of
[[Page 51111]]
HRSNs data. This activity aligns with our other efforts beyond the
acute care setting, including the CY 2023 Medicare Advantage and Part D
final rule in which we finalized the policy requiring that all Special
Needs Plans (SNPs) include one or more questions on housing stability,
food security, and access to transportation in their health risk
assessment using questions from a list of screening instruments
specified in sub-regulatory guidance (87 FR 27726 through 27740) as
well as the CY 2023 Physician Fee Schedule (PFS) final rule in which we
adopted the Screening for Social Drivers of Health measure in the
Merit-based Incentive Payment System (MIPS) (87 FR 70054 through
70055).
The Social Drivers of Health measures (as set forth in this section
VI.D.3 and section VI.D.4. of this final rule) will encourage IPFs to
identify patients with HRSNs, who are known to experience the greatest
risk of poor health outcomes, thereby improving the accuracy of high-
risk prediction calculations. Improvement in risk prediction has the
potential to reduce healthcare access barriers, address the
disproportionate expenditures attributed to people with greatest risk,
and improve the IPF's quality of care.125 126 127 128
Further, these data could guide future public and private resource
allocation to promote targeted collaboration among IPFs, health
systems, community-based organizations, and others in support of
improving patient outcomes. We believe that this screening is
especially important for IPF patients because patients with psychiatric
conditions have an increased risk of having HRSNs.\129\
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\125\ Baker, M.C., Alberti, P.M., et al. (2021). Social
Determinants Matter for Hospital Readmission Policy: Insights From
New York City. Health Affairs, 40(4), 645-654. Available at: https://doi.org/10.1377/hlthaff.2020.01742. Accessed on February 20, 2023.
\126\ Hammond, G., Johnston, K., et al. (2020). Social
Determinants of Health Improve Predictive Accuracy of Clinical Risk
Models for Cardiovascular Hospitalization, Annual Cost, and Death.
Circulation: Cardiovascular Quality and Outcomes, 13 (6) 290-299.
Available at: https://doi.org/10.1161/CIRCOUTCOMES.120.006752.
Accessed on February 20, 2023.
\127\ Hill-Briggs, F. (2021). Social Determinants of Health and
Diabetes: A Scientific Review. Diabetes Care. Available at: https://diabetesjournals.org/care/article/44/1/258/33180/Social-Determinants-of-Health-and-Diabetes-A. Accessed on February 20,
2023.
\128\ Jaffrey, J.B., Safran, G.B., Addressing Social Risk
Factors in Value-Based Payment: Adjusting Payment Not Performance to
Optimize Outcomes and Fairness. Health Affairs Blog, April 19, 2021.
Available at: https://www.healthaffairs.org/do/10.1377/forefront.20210414.379479/full/. Accessed on February 20, 2023.
\129\ Adepoju, OE, Liaw, W, et al. (2022) Assessment of Unmet
Health-Related Social Needs Among Patients with Mental Illness
Enrolled in Medicare Advantage. Available at: https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2798096.
Accessed on December 7, 2022.
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In the FY 2023 IPF PPS final rule, we observed that the Hospital
IQR Program had proposed two Social Drivers of Health measures and
stated that we would consider these measures for the IPFQR Program in
the future (87 FR 46873). The first of these two measures is the
Screening for Social Drivers of Health measure, which assesses the
percent of patients admitted to the hospital who are 18 years or older
at time of admission and are screened for food insecurity, housing
instability, transportation needs, utility difficulties, and
interpersonal safety.
Utilization of screening tools to identify the burden of unmet
HRSNs can be a helpful first step for IPFs in identifying necessary
community partners and connecting individuals to resources in their
communities. We believe collecting data across the same five HRSN
domains that were screened under the AHC Model and adopted for acute
care hospitals in the Hospital IQR Program will illuminate their impact
on health outcomes and disparities and the healthcare cost burden for
IPFs, particularly for IPFs that serve patients with disproportionately
high levels of social risk, given that patients with serious mental
illness are especially vulnerable to and affected by HRSNs. In
addition, data collection in the IPF care setting could inform
meaningful and sustainable solutions for provider-types participating
in other quality reporting programs to close equity gaps among the
communities they serve.130 131 132 133 134
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\130\ The Physicians Foundation: 2020 Survey of America's
Patients, Part Three. Available at: https://physiciansfoundation.org/wp-content/uploads/2020/10/2020-Physicians-Foundation-Survey-Part3.pdf.
\131\ Office of the Assistant Secretary for Planning and
Evaluation (ASPE) (2020). Report to Congress: Social Risk Factors
and Performance Under Medicare's Value-Based Purchasing Program
(Second of Two Reports). Available at: https://aspe.hhs.gov/pdf-report/second-impact-report-to-congress.
\132\ Billioux, A., Verlander, K., Anthony, S., & Alley, D.
(2017). Standardized Screening for Health-Related Social Needs in
Clinical Settings: The Accountable Health Communities Screening
Tool. NAM Perspectives, 7(5). Available at: https://doi.org/10.31478/201705b.
\133\ Baker, M.C., Alberti, P.M., Tsao, T.Y., Fluegge, K.,
Howland, R.E., & Haberman, M. (2021). Social Determinants Matter for
Hospital Readmission Policy: Insights From New York City. Health
Affairs, 40(4), 645-654. Available at: https://doi.org/10.1377/hlthaff.2020.01742.
\134\ De Marchis, E., Knox, M., Hessler, D., WillardGrace, R.,
Oliyawola, JN, et al. (2019). Physician Burnout and Higher Clinic
Capacity to Address Patients' Social Needs. The Journal of the
American Board of Family Medicine, 32 (1), 69-78.
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For data collection of the Screening for Social Drivers of Health
measure, IPFs could use a self-selected screening tool and collect
these data in multiple ways, which can vary to accommodate the
population they serve and their individual needs. One example of a
potential screening tool for IPFs to collect data on the Screening for
Social Drivers Health Measure is the AHC Model's standard 10-item AHC
Health-Related Social Needs Screening Tool (AHC HRSN Screening Tool),
which enables providers to identify HRSNs in the five core domains
(described in Table 18) among community-dwelling Medicare, Medicaid,
and dually eligible beneficiaries. The AHC Model, including its
screening tool, was tested across many care delivery sites in diverse
geographic locations across the United States. More than one million
Medicare and Medicaid beneficiaries have been screened using the AHC
HRSN Screening Tool, which was evaluated psychometrically and
demonstrated evidence of both reliability and validity, including
inter-rater reliability and concurrent and predictive validity.
Moreover, the AHC HRSN Screening Tool can be implemented in a variety
of places where patients seek healthcare, including inpatient
psychiatric facilities.
The intent of the Screening for Social Drivers of Health measure is
to promote adoption of HRSN screening by IPFs. We encourage IPFs to use
the screening as a basis for developing their own individual action
plans (for example, navigation services and subsequent referral), as
well as an opportunity to initiate or improve partnerships with
community-based service providers. We believe that this measure will
yield actionable information to close equity gaps by encouraging IPFs
to identify patients with HRSNs, with a reciprocal goal of
strengthening linkages between IPFs and local community-based partners
to promptly connect patients and families to the support they need.
Both the Screening for Social Drivers of Health measure and the
Screen Positive Rate for Social Drivers of Health measure, discussed in
VI.D.4. of this final rule, address our Meaningful Measures Framework's
\135\ quality priority of ``Work with Communities to Promote Best
Practices of Healthy Living'' through the Meaningful Measures Area of
``Equity of Care.'' Additionally, pursuant to our Meaningful Measures
2.0, these Social Drivers of Health measures address the
[[Page 51112]]
equity priority area and align with our commitment to introduce plans
to close health equity gaps and promote equity through quality
measures, including to ``develop and implement measures that reflect
social and economic determinants.'' \136\ Development, proposal, and
adoption of these measures also aligns with our strategic pillar to
advance health equity by addressing the health disparities that
underlie our health system.\137\ Further, inclusion of these measures
in the IPFQR Program aligns with these measures' adoption in the
Hospital IQR Program in the FY 2023 IPPS/LTCH final rule (87 FR 49202
through 49215).
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\135\ Centers for Medicare & Medicaid Services. Meaningful
Measures Framework. Available at: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/QualityInitiativesGenInfo/CMS-Quality-Strategy.
\136\ Centers for Medicare & Medicaid Services. Meaningful
Measures 2.0: Moving from Measure Reduction to Modernization.
Available at: https://www.cms.gov/meaningful-measures-20-moving-measure-reduction-modernization.
\137\ Brooks-LaSure, C. (2021). My First 100 Days and Where We
Go From Here: A Strategic Vision for CMS. Available at: https://www.cms.gov/blog/my-first-100-days-and-where-we-go-here-strategic-vision-cms.
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The Screening for Social Drivers of Health measure (alongside the
Screen Positive Rate for Social Drivers of Health measure described in
section VI.D.4 of this final rule) will be the first measurement of
social drivers of health in the IPFQR Program. We believe these
measures are appropriate for measurement of the quality of care
furnished by IPFs. Screening patients for HRSNs during inpatient
hospitalization in an IPF will allow healthcare providers, including
IPFs, to identify and potentially help address HRSNs for this medically
underserved patient population as part of discharge planning and
contribute to long-term improvements in patient outcomes. Identifying
and addressing HRSNs for patients receiving care in IPFs could have a
direct and positive impact on IPFs' quality performance because of
improvements in patient outcomes that could occur when patients' HRSNs
are reduced. Moreover, collecting aggregate data on the HRSNs of IPF
patient populations via these measures is crucial in informing design
of future measures that could enable us to set appropriate performance
targets for IPFs with respect to closing the gap on health equity.
b. Overview of Measure
The Screening for Social Drivers of Health measure assesses whether
an IPF implements screening for all patients who are 18 years or older
at time of admission for food insecurity, housing instability,
transportation needs, utility difficulties, and interpersonal safety.
To report on this measure, IPFs will provide: (1) the number of
inpatients admitted to the facility who are 18 years or older at time
of admission and who are screened for all of the five HRSNs (food
insecurity, housing instability, transportation needs, utility
difficulties, and interpersonal safety); and (2) the total number of
patients who are admitted to the facility who are 18 years or older on
the date they are admitted.
Measure specifications for the Screening for Social Drivers of
Health measure, which were available during the review of the MUC List,
are available at https://mmshub.cms.gov/sites/default/files/map-hospital-measure-specifications-manual-2022.pdf.
(1) Measure Calculation
(a) Cohort
The Screening for Social Drivers of Health measure assesses the
total number of patients aged 18 years and older, screened for HRSNs
(specifically, food insecurity, housing instability, transportation
needs, utility difficulties, and interpersonal safety) during an IPF
stay.
(b) Numerator
The numerator of the Screening for Social Drivers of Health measure
consists of the number of patients admitted to an IPF stay who are 18
years or older on the date of admission and are screened during their
IPF stay for all of the following five HRSNs: food insecurity, housing
instability, transportation needs, utility difficulties, and
interpersonal safety.
(c) Denominator
The denominator of the Screening for Social Drivers of Health
measure consists of the number of patients who are admitted to an IPF
stay and who are 18 years or older on the date of admission. The
following patients are excluded from the denominator: (1) patients who
opt-out of screening; and (2) patients who are themselves unable to
complete the screening during their inpatient stay and have no legal
guardian or caregiver able to do so on the patient's behalf during
their IPF stay.
(d) Calculation
The Screening for Social Drivers of Health measure is calculated as
the number of patients admitted to an IPF stay who are 18 years or
older on the date of admission screened for all five HRSNs (food
insecurity, housing instability, transportation needs, utility
difficulties, and interpersonal safety) divided by the number of
patients 18 years or older on the date of admission admitted to the
IPF.
(2) Review by the Measure Applications Partnership
We included the Screening for Social Drivers of Health measure on
the publicly available ``List of Measures Under Consideration for
December 1, 2022'' (MUC List), a list of measures under consideration
for use in various Medicare programs.\138\ The CBE-convened MAP Health
Equity Advisory Group reviewed the MUC List including the Screening for
Social Drivers of Health measure (MUC 2022-053) in detail on December 6
through 7, 2022.\139\ The MAP Health Equity Advisory Group expressed
support for the collection of data related to social drivers of health,
but raised concerns regarding public reporting of these data and
potential repetition of asking patients the same questions across
settings.\140\
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\138\ Centers for Medicare & Medicaid Services. List of Measures
Under Consideration for December 1, 2022. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\139\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\140\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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In addition, on December 8 through 9, 2022, the MAP Rural Health
Advisory Group reviewed the 2022 MUC List and the MAP Hospital
Workgroup did so on December 13 through 14, 2022.\141\ The MAP Rural
Health Advisory Group noted some potential reporting challenges
including the potential masking of health disparities that are
underrepresented in some areas and that sample size and populations
served may be an issue, but expressed that the Screening for Social
Drivers of Health measure serves as a starting point to determine where
screening is occurring. The MAP Hospital Workgroup expressed strong
support for the measure but noted that interoperability will be
important and cautioned about survey fatigue. The MAP Hospital
Workgroup members conditionally supported the measure pending: (1)
testing of the measure's reliability and validity; (2) endorsement by
the CBE; (3) additional details on how potential tools map to the
individual HRSNs, as well as best practices; (4) identification of
resources that may be available to assist patients with identified
HRSNs; and (5)
[[Page 51113]]
the measure's alignment with data standards, particularly the GRAVITY
project.\142\ The GRAVITY project's mission statement is ``to serve as
the open public collaborative advancing health and social data
standardization for health equity.'' \143\ Thereafter, the MAP
Coordinating Committee deliberated on January 24 through 25, 2023, and
ultimately voted to uphold the MAP Hospital Workgroup's recommendation
to conditionally support for rulemaking with the same conditions.\144\
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\141\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\142\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\143\ https://thegravityproject.net/.
\144\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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We believe this measure establishes an important foundation for
prioritizing the achievement of health equity among IPFs. Our approach
to developing health equity measures is incremental, and we believe
that health care equity outcomes in the IPFQR Program will inform
future efforts to advance and achieve health care equity by IPFs. We
additionally believe this measure to be a building block that lays the
groundwork for a future meaningful suite of measures that would assess
IPF progress in providing high-quality healthcare for all patients,
regardless of social risk factors or demographic characteristics.
(3) CBE Endorsement
We have not submitted this measure for CBE endorsement at this
time. Although section 1886(s)(4)(D)(i) of the Act generally requires
that measures specified by the Secretary must be endorsed by the entity
with a contract under section 1890(a) of the Act, section
1886(s)(4)(D)(ii) of the Act, states that in the case of a specified
area or medical topic determined appropriate by the Secretary for which
a feasible and practical measure has not been endorsed by the entity
with a contract under section 1890(a) of the Act, the Secretary may
specify a measure that is not so endorsed as long as due consideration
is given to a measure that has been endorsed or adopted by a consensus
organization identified by the Secretary. We reviewed measures endorsed
by consensus organizations and were unable to identify any other
measures on this topic endorsed by a consensus organization and
therefore, we believe the exception in section 1886(s)(4)(D)(ii) of the
Act applies.
c. Data Collection, Submission and Reporting
We believe incremental implementation of the Screening for Social
Drivers of Health measure, by permitting one year of voluntary
reporting prior to mandatory reporting, will allow IPFs who are not yet
screening patients for HRSNs to get experience with collecting data for
this measure and equally allow IPFs who already undertake screening
efforts to report data already being collected. Therefore, we proposed
voluntary reporting of this measure beginning with the data collected
in CY 2024, which would be reported to CMS in CY 2025, followed by
mandatory reporting beginning with data collected in CY 2025, which
would be reported to CMS in CY 2026 for the FY 2027 payment
determination.
Due to variability across IPFs and the populations they serve, and
in alignment with the Hospital IQR Program, we will allow IPFs
flexibility with the selection of tools to screen patients for food
insecurity, housing instability, transportation needs, utility
difficulties, and interpersonal safety. Potential sources of these data
could include, for example, administrative claims data, electronic
clinical data, standardized patient assessments, or patient-reported
data and surveys.
Multiple screening tools for health-related social needs (HRSNs)
already exist. For additional information on resources, we refer
readers to evidence-based resources like the Social Interventions
Research and Evaluation Network (SIREN) website, for example, for
comprehensive information about the most widely used HRSN screening
tools.145 146 SIREN contains descriptions of the content and
characteristics of various tools, including information about intended
populations, completion time, and number of questions.
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\145\ Social Interventions Research & Evaluation Network.
(2019). Social Needs Screening Tool Comparison Table. Available at:
https://sirenetwork.ucsf.edu/tools-resources/resources/screening-tools-comparison. Accessed January 18, 2021.
\146\ The Social Interventions Research and Evaluation Network
(SIREN) at University of California San Francisco was launched in
the spring of 2016 to synthesize, disseminate, and catalyze research
on SDOH and healthcare delivery.
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We encourage IPFs to consider digital standardized screening tools
and refer readers to the FY 2023 IPPS/LTCH PPS final rule (87 FR 49207
through 49208) where we discuss how the use of certified health
information technology (IT), including but not limited to certified EHR
technology, can support capture of HRSN information in an interoperable
fashion so that these data can be shared across the care continuum to
support coordinated care. We also encourage readers to learn about the
United States Core Data for Interoperability (USCDI) standard used in
certified health IT and how this standard can support interoperable
exchange of health and HRSN assessment data.\147\
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\147\ Office of the National Coordinator for Health IT (ONC).
United States Core Data for Interoperability. Accessed at: https://www.healthit.gov/isa/united-states-core-data-interoperability-uscdi.
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We proposed that IPFs would report aggregate data on this measure,
that is IPFs would report aggregated data for the numerator and the
denominator to CMS (as described in section VI.D.3.b.(1). of this final
rule) but would not be required to report patient-level data. IPFs are
required to submit information for chart-abstracted measures once
annually using a CMS-approved web-based data collection tool available
within the HQR System (previously referred to as the QualityNet Secure
Portal). We refer readers to section VI.I of this final rule (Form,
Manner, and Timing of Quality Data Submission) for more details on our
previously finalized data submission and deadline requirements across
measure types.
We invited public comment on this proposal.
Comment: Many commenters supported adoption of the Screening for
Social Drivers of Health measure. Some commenters stated that screening
for these HRSNs will help IPFs better understand patients' needs,
improve care coordination with outpatient and community resources,
increase the dignity and respect with which patients are treated, and
support development of patient-centered treatment plans. One commenter
stated that the data collected through these screenings could help IPFs
shape facility level goals associated with health equity and empower
the workforce to recognize and eliminate health disparities. One
commenter specifically supported the flexibility with respect to tool
selection and stated that this will help IPFs select the standardized
screening instruments most applicable for their individual patient
populations. Another commenter stated that discharge will not lead to
positive patient outcomes if the patient is discharged to unstable
conditions or without the transportation necessary to access support
services.
Response: We thank commenters for their support of the Screening
for Social Drivers of Health measure. We agree that HRSNs are critical
factors that
[[Page 51114]]
impact patient outcomes, and increased knowledge about patients' HRSNs
will help IPFs shape goals associated with health equity. Further, we
agree that collecting these data will help IPFs improve coordination
with outpatient and community resources to better deliver patient-
centered care. Finally, we note that these activities would support
IPFs' execution of responsibilities related to the required standard
for social services under 42 CFR 482.62(f).
Comment: Several commenters recommended that CMS conduct additional
testing, specifically in the IPF setting, to ensure that the measure
addresses the specific needs of the IPF patient population.
Response: We acknowledge that this measure was initially developed
for the general acute care setting. While we recognize the value of
measures undergoing testing and evaluation of validity and feasibility
in the setting for which they are being adopted, given the urgency of
identifying and addressing HRSNs described in section VI.D.4.a of this
final rule, and, as there are currently no other existing measures that
address Screening for Social Drivers of Health, we believe it is
important to implement this measure as soon as feasible. We believe
that this measure is equally applicable to freestanding IPFs and
psychiatric units within acute care facilities as to general acute care
settings, because we believe that identifying the HRSNs of IPF patients
will be equally valuable in understanding patients' needs, improving
care coordination with outpatient and community resources, increasing
the dignity and respect with which patients are treated, and supporting
development of patient-centered treatment plans as identifying the
HRSNs of acute care hospital patients. We note that identifying and
addressing HRSNs is a critical topic for patients treated in IPFs and
that there are high levels of health disparities experienced by this
patient population. CMS will monitor measure implementation and data
reporting as part of standard program and measure review and will
consider updates to the measure if improvements are identified through
this process.
Comment: Many commenters expressed concern that this measure has
not received endorsement by the CBE.
Response: While we recognize the value of measures undergoing
review for potential CBE endorsement, given the urgency of achieving
health equity, we believe it is important to implement this measure
with voluntary reporting beginning with the CY 2024 reporting period
followed by mandatory reporting beginning with the CY 2025 reporting
period/FY 2027 payment determination. We note that, under section
1886(s)(4)(D)(ii) of the Act, the Secretary may specify a measure that
is not so endorsed as long as due consideration is given to measures
that have been endorsed or adopted by a consensus organization
identified by the Secretary. We reviewed measures endorsed by consensus
organizations and were unable to identify any other measures on this
topic endorsed by a consensus organization, and therefore, we believe
the exception in section 1886(s)(4)(D)(ii) of the Act applies.
Comment: Many commenters recommended extending the voluntary
reporting phase for this measure.
Response: Beginning to collect the data remains imperative as we
continue to build on our strategic pillar to advance health equity by
addressing the health disparities that underlie our health system. We
therefore have determined that the proposed voluntary and mandatory
reporting periods prioritize the urgency of capturing social drivers of
health data and taking actionable steps towards closing the health
equity gap.
Comment: Some commenters recommended that CMS defer adoption of
this measure until the Hospital IQR Program's voluntary reporting
period for its version of this measure concludes to allow CMS and IPFs
to identify best practices for screening patients and collecting HRSNs
data in a minimally burdensome way. Some of these commenters stated
that IPFs often have fewer resources available for such data collection
relative to acute care hospitals. Other commenters recommended engaging
IPFs to voluntarily test the measure to ensure usability,
acceptability, and face validity are met for this setting.
Response: We acknowledge commenters' desire to be able to learn
from the experiences of acute care hospitals reporting this measure.
Hospitals participating in the Hospital IQR Program that choose to
voluntarily report this measure will have already reported data in CY
2024 (87 FR 49207). Furthermore, the Hospital IQR Program finalized
mandatory reporting of this measure for the FY 2026 payment
determination (that is data submitted in CY 2025 representing the CY
2024 performance period) (87 FR 49207). Given the timing of reporting
this measure in the Hospital IQR Program, we believe that IPFs will
have the opportunity to learn from the experiences of acute care
hospitals, including best practices for collecting HRSNs data, prior to
mandatory reporting for the IPFQR Program for the FY 2027 payment
determination. Furthermore, we believe that the voluntary reporting of
CY 2024 data submitted to CMS in CY 2025 for the IPFQR Program will
provide additional opportunities to identify minimally burdensome
screening instruments and data collection practices. Finally, we note
that we will monitor measure implementation and data reporting as part
of standard program and measure review and will consider updates to the
measure if improvements are identified through this process. Therefore,
we do not believe that the benefits of extending voluntary reporting of
this measure in the IPFQR Program for more than one year outweigh the
potential detriments associated with delay in measure adoption that
extending the voluntary reporting period would require.
Comment: Several commenters had recommendations related to the
specifications for the Screening for Social Drivers of Health measure
regarding the frequency and timing of administering these screenings.
One commenter recommended not requiring individual patients to be
screened more frequently than once per quarter so that patients who are
readmitted or admitted to other settings over a short duration are not
repeatedly screened when their HRSNs are unlikely to have changed.
Another commenter recommended that for patients who have long stays
(sometimes greater than one year) the measure should be updated to
require an annual screening and screening at discharge. This commenter
stated that for these patients screening at discharge would provide
data which would inform discharge planning.
Response: We understand the commenters' concerns, especially given
the frequency of unmet HRSNs among psychiatric patients, regarding
patients who may be screened frequently, or whose screening results may
change significantly during their inpatient stay (such as those
patients with long duration stays). We note that screening can occur
any time during the hospital admission prior to discharge. Further, for
patients frequently admitted to inpatient facilities, the IPF could
confirm the current status of any previously reported HRSNs and inquire
about other HRSNs not previously reported or that may have changed in
the intervening period. For additional information on how to apply and
report these screenings, we refer readers to the Hospital IQR Program's
Frequently Asked Questions document regarding this measure in the
Hospital IQR
[[Page 51115]]
Program, available at: We will develop a similar Frequently Asked
Questions document for IPFs as part of providing educational and
training materials; this document will be conveyed through routine
communication channels to hospitals, vendors, and QIOs, including, but
not limited to, issuing memos, emails, and notices on a CMS website.
Comment: Several commenters recommended additional changes to the
measure specifications. Due to the sensitive nature of screening for
risk of interpersonal violence, commenters recommended changes that
included removing this domain from the measure specifications, and
updating the measure to ensure patient privacy when responding to this
screening question, either by excluding patients who could not respond
to the question confidentially, or by ensuring responses remain hidden
in all records and handouts accessible to patients. One commenter
recommended removing the exclusion language ``and lack of a guardian or
caregiver available to do so on the patient's behalf'' because such a
guardian or caregiver may provide inaccurate information about the
patient's risk of interpersonal violence. One commenter recommended
excluding patients coming from or being discharged to long-term care
settings because these patients would be at lower risk for these five
HRSNs. Another commenter recommended expanding the measure to include
screening for lack of financial resources.
Response: We have prioritized selection of the proposed five HRSN
domains based on existing evidence from both the AHC Model, including
recommendations from a technical expert panel (TEP) that informed the
initial selection, and emerging evidence of correlations between given
social drivers of health and worse health outcomes and social drivers
of health for which interventions have shown marked improvements in
health outcomes and healthcare utilization (88 FR 21280). Through this
process we did not identify lack of financial resources as being one of
the social drivers of health that met our criteria for selection (these
criteria are set forth in section V.D.3.a. of the proposed rule and in
section VI.D.3 of this final rule); therefore, we did not include it in
the Screening for Social Drivers of Health measure. We note that while
the Screening for Social Drivers of Health measure requires screening
for the five identified HRSNs, IPFs may screen for additional HRSNs
that they believe are relevant for their patient population and the
community in which they serve, and that standardized screening
instruments such as those available for screening for these five HRSNs
may also include a screening for lack of financial resources. For
example, the Accountable Health Communities screening tool includes
questions for eight supplemental domains, including financial strain.
Furthermore, we note that this measure is a first step towards
development of a long-term strategy to integrate social drivers of
health and HRSN data into quality performance measurement and is part
of our broader commitment to health equity.
We believe it is imperative that IPFs screen for all five domains
established in this measure. We understand commenters' concerns
regarding the sensitive nature of screening for risk of interpersonal
violence and agree that patient safety must remain the IPF's principal
concern. We recommend that IPFs ensure that patients feel that they are
safe answering questions and remind patients that they may opt out of
the screening for any reason. We note that, because IPFs likely are
covered entities under the Health Insurance Portability and
Accountability Act of 1996 (HIPAA) Rules (codified at 45 CFR parts 160
and 164),\148\ information provided by patients in response to
screening for this measure would be protected health information
(PHI).\149\ Therefore, IPFs are responsible for adopting reasonable
safeguards to ensure that patients' PHI is not impermissibly disclosed
contrary to applicable confidentiality, security, and privacy laws.
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\148\ For more information on the three HIPAA rules, we refer
readers to the HIPAA for Professionals site at: https://www.hhs.gov/hipaa/for-professionals/.
\149\ https://www.hhs.gov/answers/hipaa/what-is-phi/.
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We do not believe it would be appropriate to remove the exclusion
which would allow a caregiver or guardian to provide information on a
patient's behalf if the patient is unable to do so. While we agree that
the scenario presented by commenters (that is, a guardian or caregiver
may provide inaccurate information about the patient's risk of
interpersonal violence) is possible, we do not believe that the
potential unintended consequence of capturing inaccurate data for this
HRSN for a small portion of patients outweighs the potential benefit of
capturing accurate data regarding all of these five HRSNs for as many
patients as possible, including those who are unable to respond to the
screening without the assistance of a caregiver or guardian.
Finally, we believe that it is appropriate to assess the HRSNs of
all eligible patients (that is, patients who are over 18 years of age
at admission and do not meet the measure's exclusion criteria)
including patients being admitted from or discharged to long-term care
settings. While these patients are at lower risk during their stay in
the long-term care facility, we believe it is appropriate for the IPF
to assess the patient's overall risk of unmet HRSNs. We note, for
example, that the AHC screening instrument assesses the patient's HRSNs
over the past 12 months for the majority of the HRSNs included in this
tool. Therefore, screening patients admitted from or being discharged
to long-term care settings could help identify unmet HRSNs among this
patient population. We will continue to take all concerns, comments,
and suggestions into account and will consider them as part of any
potential future modifications to these measures or potential new
measure development in future notice-and-comment rulemaking.
Comment: One commenter recommended that the Screening for Social
Drivers of Health measure be completed by a peer support specialist to
engender trust and create a safe environment.
Response: We agree with the commenter that it is important for the
screening for HRSNs to be accomplished in a way that engenders trust
and creates a safe environment. We recommend that IPFs evaluate the
requirements for administration (such as whether the screening
instrument can be administered by peer support specialists) as part of
their instrument selection process. We note that the AHC instrument
described in section VI.D.3 of this rule allows administration by
clinicians and staff \150\ and would allow administration by peer
support specialists.
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\150\ https://nam.edu/standardized-screening-for-health-related-social-needs-in-clinical-settings-the-accountable-health-communities-screening-tool/.
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Comment: One commenter recommended aligning SDOH related measures,
including this one, across programs including programs for the
ambulatory setting (including MIPS).
Response: We agree with the commenter that addressing patients'
HRSNs is important in all settings in which patients access care. We
note that this measure was adopted into MIPS in the CY 2023 Physician
Fee Schedule (PFS) final rule (87 FR 70055) as well as the Hospital IQR
Program in the FY 2023 IPPS/LTCH PPS final rule (87 FR 49215). In
addition, we have proposed to adopt this measure in the PPS-Exempt
Cancer Hospital Quality Reporting Program in the FY 2024 IPPS/
[[Page 51116]]
LTCH PPS proposed rule (88 FR 27128) and the End-Stage Renal Disease
Quality Incentive Program in the CY 2024 ESRD PPS proposed rule (88 FR
42515). We note that only the IPFQR Program is the subject of this
final rule, and the commenter's recommendation is therefore beyond the
scope of this final rule.
Comment: One commenter recommended against public reporting until a
standardized, validated instrument is adopted so the data are collected
using a uniform tool. One commenter requested that CMS provide guidance
on which available, standardized assessment instruments address each of
the domains.
Response: We are sensitive to the concerns raised by commenters
about the lack of clarity about which screening instrument IPFs should
use in order to screen for HRSNs. We acknowledge the challenges that
lack of standardization across screening instruments or data collection
practices may introduce in the consistency of the information collected
across IPFs. While we acknowledge the potential benefits of a single
screening instrument or prescribed set of standards, we also recognize
the benefits of providing IPFs with flexibility to customize screening
and data collection to their local community contexts and patient
populations, especially in the initial stages of implementing screening
protocols. We encourage IPFs to prioritize screening tools that have
undergone thorough testing to ensure they are accurate and reliable. We
believe that this measure should promote high-quality screening
practices which, among other things, ensure accurate identification of
unmet social needs.
For selecting a screening tool, we suggest that IPFs refer to
evidence-based resources for comprehensive information about the most
widely used HRSN screening tools. For example, the Social Interventions
Research and Evaluation Network (SIREN) website,\151\ housed at the
Center for Health and Community at the University of California, San
Francisco, contains descriptions of the content and characteristics of
various tools, including information about intended populations,
completion time, and number of questions.
---------------------------------------------------------------------------
\151\ https://chc.ucsf.edu/siren.
---------------------------------------------------------------------------
Comment: Several commenters stated that a measurement of whether a
screening occurred does not indicate whether the needs have been met
nor the impact of these specific HRSNs on the patient's health
outcomes. Some of these commenters also stated that the lack of
resources faced by IPFs may lead IPFs to screen for SDOH for which they
are unable to assist patients. These commenters expressed concern that
this may be frustrating for patients who would expect the IPF to
address these needs after the screening.
Response: During the development of both Social Drivers of Health
measures, we gave this topic significant consideration. The intent of
the two measures is to promote adoption of screening patients for HRSNs
by healthcare providers as well as taking action to connect patients
who identify one or more HRSNs with available resources. Evaluation of
the AHC Model concluded that universal screening may identify needs
that would otherwise remain undetected.\152\ While broad availability
of community-based resources that address patients' health-related
social needs would be ideal, we believe that one of the benefits of
collecting data from screening for HRSNs will be identification of
opportunities to enable meaningful action, including prioritizing and
investing in such resources. Beginning to collect the data on patients'
HRSNs remains imperative and a crucial step in developing resources for
advancing health equity. Such data collection has already allowed some
entities to reallocate resources to address particular HRSNs that
disproportionately affect a given patient population or geographic
region, as noted in the FY 2023 IPPS/LTCH PPS final rule, in which the
Hospital IQR Program adopted these measures (87 FR 49213).
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\152\ RTI International. (2020). Accountable Health Communities
(AHC) Model Evaluation. Available at: https://innovation.cms.gov/data-and-reports/2020/ahc-first-eval-rpt.
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Comment: One commenter requested clarification of whether the
measure will represent the ``total number'' of patients screened for
SDOH or the proportion of patients screened for SDOH.
Response: IPFs will report the aggregate numerator for this measure
(that is, the total number of patients admitted to an IPF stay who are
18 years or older on the date of admission and screened for all five
HRSNs), and the aggregate denominator (that is, number of patients who
are admitted to an IPF stay and who are 18 years or older on the date
of admission). Using these data and the denominator exclusions (that
is, patients who opt-out of screening and patients who are themselves
unable to complete the screening during their inpatient stay and have
no legal guardian or caregiver able to do so on their behalf during
their IPF stay), we will calculate the screening rate (that is, the
proportion of patients screened for all five SDOH) for this measure.
Comment: One commenter did not support this measure because of
their concern that the specific HRSNs in the Screening for Social
Drivers of Health measure are not completely aligned with the HL7
Gravity Project.
Response: We have prioritized the five HRSN domains in this measure
based on existing evidence from the AHC Model including recommendations
from a TEP that informed the initial selection. We commend additional
initiatives currently underway to expand capabilities to capture
additional social drivers of health data elements, including the
Gravity Project. We note that the five domains covered by the Screening
for Social Drivers of Health measure are included within the ``social
risk domains'' of the Gravity Project. We support harmonization of data
regarding HRSNs for interoperable electronic health information
exchange that will meet information exchange standards.
Comment: One commenter did not support this measure stating their
belief that there is a lack of evidence that screening impacts quality
of care provided by IPFs.
Response: We note that the two Social Drivers of Health measures
are derived from existing evidence from both the AHC Model and emerging
evidence of correlations between the designated social drivers of
health and higher healthcare utilization of emergency departments and
hospitals, worse health outcomes and/or drivers of health for which
interventions have shown marked improvements in health outcomes and
health care utilization (88 FR 21280).
Comment: One commenter did not support required reporting of these
data because, while the commenter agreed that screening for SDOH is
important and should be occurring in the IPF setting, the commenter
expressed concern that reporting these data is too burdensome and takes
away from patient care. Another commenter did not support the Screening
for Social Drivers of Health measure because IPF stays are typically
only a few days, and the commenter stated their belief that there is
therefore insufficient time to complete these screenings during the
stay.
Response: While we understand implementation of HRSN screening
processes and reporting of the SDOH measures is associated with some
burden, as discussed in sections VII.B.
[[Page 51117]]
and VIII.A of this final rule, we believe the benefits outweigh the
burden, as screening for and identifying patients' HRSNs is a critical
step towards treating the whole patient, improving clinical outcomes,
improving equitable care, and ultimately eliminating disparities in
health outcomes among populations that have been historically
underserved by the healthcare system.
We note that screening can occur any time during the IPF admission
prior to discharge and that, for example, the AHC Screening Tool
addresses these 5 HRSNs using a total of 10 questions. Therefore, we
believe that IPFs will be able to find sufficient time during the
patient's IPF stay to administer this or a similar screening tool for
SDOH.
Final Decision: After consideration of the public comments we
received, we are finalizing adoption of the Screening for Social
Drivers of Health measure as proposed.
4. Adoption of the Screen Positive Rate for Social Drivers of Health
Measure Beginning With Voluntary Reporting of CY 2024 Data and Followed
by Mandatory Reporting Beginning With CY 2025 Data/FY 2027 Payment
Determination
a. Background
The impact of social risk factors on health outcomes has been well-
established in the literature.153 154 155 156 157 The
Physicians Foundation reported that 73 percent of the physician
respondents to the 2021 iteration of their annual survey agreed that
social risk factors like housing instability and food insecurity would
drive health services demand.\158\ Recognizing the need for a more
comprehensive approach to eliminating the health equity gap, we have
prioritized quality measures that would capture social risk factors and
facilitate assessment of their impact on health outcomes and
disparities and healthcare utilization and costs.159 160 161
Specifically, in the inpatient setting, we aim to encourage systematic
identification of patients' HRSNs (as defined in section VI.D.3.a. of
this final rule) as part of discharge planning with the intention of
promoting linkages with relevant community-based services that address
those needs and support improvements in health outcomes following
discharge from the IPF.
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\153\ Institute of Medicine 2014. Capturing Social and
Behavioral Domains and Measures in Electronic Health Records: Phase
2. Washington, DC: The National Academies Press. Available at:
https://doi.org/10.17226/18951.
\154\ Centers for Medicare & Medicaid Services. (2021).
Accountable Health Communities Model. Accountable Health Communities
Model [verbar] CMS Innovation Center. Available at: https://innovation.cms.gov/innovation-models/ahcm. Accessed November 23,
2021.
\155\ Kaiser Family Foundation. (2021). Racial and Ethnic Health
Inequities and Medicare. Available at: https://www.kff.org/medicare/report/racial-and-ethnic-health-inequities-and-medicare/. Accessed
November 23, 2021.
\156\ Milkie Vu et al. Predictors of Delayed Healthcare Seeking
Among American Muslim Women, Journal of Women's Health 26(6) (2016)
at 58; Nadimpalli SB, Cleland CM, Hutchinson MK, Islam N, Barnes LL,
Van Devanter N. (2016) The Association between Discrimination and
the Health of Sikh Asian Indians. Health Psychology, 35(4), 351-355.
https://doi.org/10.1037/hea0000268.
\157\ Office of the Assistant Secretary for Planning and
Evaluation (ASPE). (2020). Report to Congress: Social Risk Factors
and Performance Under Medicare's Value-Based Purchasing Program
(Second of Two Reports). Available at: https://aspe.hhs.gov/pdf-report/second-impact-report-to-congress.
\158\ The Physicians Foundation. (2020) 2020 Survey of America's
Patients, Part Three. Available at: https://physiciansfoundation.org/wp-content/uploads/2020/10/2020-Physicians-Foundation-Survey-Part3.pdf.
\159\ Alley, D.E., C.N. Asomugha, P.H. Conway, and D.M.
Sanghavi. 2016. Accountable Health Communities-Addressing Social
Needs through Medicare and Medicaid. The New England Journal of
Medicine 374(1):8-11. Available at: https://doi.org/10.1056/NEJMp1512532.
\160\ Centers for Medicare & Medicaid Services. (2021).
Accountable Health Communities Model. Accountable Health Communities
Model [verbar] CMS Innovation Center. Available at: https://innovation.cms.gov/innovation-models/ahcm. Accessed November 23,
2021.
\161\ Billioux, A., Verlander, K., Anthony, S., & Alley, D.
(2017). Standardized Screening for Health-Related Social Needs in
Clinical Settings: The Accountable Health Communities Screening
Tool. NAM Perspectives, 7(5). Available at: https://doi.org/10.31478/201705b.
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While the Screening for Social Drivers of Health measure (discussed
previously in section VI.D.3. of this final rule) enables
identification of individuals with HRSNs, use of the Screen Positive
Rate for Social Drivers of Health measure would allow IPFs to capture
the magnitude of these needs and even estimate the impact of
individual-level HRSNs on healthcare utilization when evaluating
quality of care.162 163 164 The Screen Positive Rate for
Social Drivers of Health measure will require IPFs to report the rates
of patients who screened positive for each of the five core HRSNs.
Reporting the screen positive rate for each of the five core HRSNs will
inform actionable planning by IPFs towards closing health equity gaps
unique to the populations they serve and enable the development of
individual patient action plans (including navigation and referral
services).
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\162\ Baker, M.C., Alberti, P.M., Tsao, T.Y., Fluegge, K.,
Howland, R.E., & Haberman, M. (2021). Social Determinants Matter for
Hospital Readmission Policy: Insights From New York City. Health
Affairs, 40(4), 645-654. Available at: https://doi.org/10.1377/hlthaff.2020.01742.
\163\ CMS. Accountable Health Communities Model. Accountable
Health Communities Model [verbar] CMS Innovation Center. Available
at: https://innovation.cms.gov/innovation-models/ahcm. Accessed
November 23, 2021.
\164\ Hammond, G., Johnston, K., Huang, K., Joynt Maddox, K.
(2020). Social Determinants of Health Improve Predictive Accuracy of
Clinical Risk Models for Cardiovascular Hospitalization, Annual
Cost, and Death. Circulation: Cardiovascular Quality and Outcomes,
13 (6) 290-299. Available at: https://doi.org/10.1161/CIRCOUTCOMES.120.006752.
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In the FY 2022 IPF PPS final rule (86 FR 42625 through 42632) and
the FY 2023 IPF PPS final rule (87 FR 46865 through 46873), we
discussed our ongoing consideration of potential approaches that could
be implemented to address health equity through the IPFQR Program. As a
result of the feedback we received, we identified the Screen Positive
Rate for Social Drivers of Health measure to help inform efforts to
address health equity.
This measure assesses the percent of patients admitted to the IPF
who are 18 years or older at time of admission who were screened for
HRSNs and who screen positive for one or more of the five HRSNs,
including food insecurity, housing instability, transportation needs,
utility difficulties, or interpersonal safety (reported as five
separate rates).\165\
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\165\ Billioux, A., Verlander, K., Anthony, S., & Alley, D.
(2017). Standardized Screening for Health Related Social Needs in
Clinical Settings: The Accountable Health Communities Screening
Tool. NAM Perspectives, 7(5). Available at: https://doi.org/10.31478/201705b.
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We refer readers to section VI.D.3 of this final rule where we
previously discussed the screening and identification process resulting
in the selection of these five domains associated with the Screen for
Social Drivers of Health measure. The Screening for Social Drivers of
Health measure forms the basis of this Screen Positive Rate for Social
Drivers of Health measure. That is, the number of patients screened for
all five HRSNs in the Screening for Social Drivers of Health measure is
the denominator of the Screen Positive Rate for Social Drivers of
Health measure described here.
The COVID-19 pandemic underscored the overwhelming impact that
these five core domains of HRSNs have on disparities, health risk,
healthcare access, and health outcomes, including premature
mortality.166 167
[[Page 51118]]
Adoption of the Screen Positive Rate for Social Drivers of Health
measure will encourage IPFs to track prevalence of specific HRSNs among
patients over time and use the data to stratify risk as part of quality
performance improvement efforts. This measure may also prove useful for
patients by providing data transparency and signifying IPFs'
familiarity, expertise, and commitment regarding these health equity
issues. This measure also has the potential to reduce healthcare
provider burden and burnout, including among IPFs and their staff, by
both acknowledging patients' non-clinical needs that nevertheless
greatly contribute to adverse clinical outcomes and linking providers
with community-based organizations to enhance patient-centered
treatment and discharge planning.168 169 170 Finally, we
believe the Screen Positive Rate for Social Drivers of Health measure
has the potential to facilitate data-informed collaboration with
community-based services and focused community investments, including
the development of pathways and infrastructure to connect patients to
local community resources.
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\166\ Kaiser Family Foundation. (2021). Racial and Ethnic Health
Inequities and Medicare. Available at: https://www.kff.org/medicare/report/racial-and-ethnic-health-inequities-and-medicare/. Accessed
November 23, 2021.
\167\ Centers for Disease Control and Prevention. (2019). CDC
COVID-19 Response Health Equity Strategy: Accelerating Progress
Towards Reducing COVID-19 Disparities and Achieving Health Equity.
July 2020. Available at: https://www.cdc.gov/coronavirus/2019-ncov/community/health-equity/cdc-strategy.html. Accessed November 17,
2021.
\168\ The Physicians Foundation. (2020). Survey of America's
Patients, Part Three. Available at: https://physiciansfoundation.org/wp-content/uploads/2020/10/2020-Physicians-Foundation-Survey-Part3.pdf.
\169\ De Marchis, E., Knox, M., Hessler, D., WillardGrace, R.,
Oliyawola, JN, et al. (2019). Physician Burnout and Higher Clinic
Capacity to Address Patients' Social Needs. The Journal of the
American Board of Family Medicine, 32 (1), 69-78.
\170\ Kung, A., Cheung, T., Knox, M., Willard-Grace, R.,
Halpern, J., et.al, (2019). Capacity to Address Social Needs Affect
Primary Care Clinician Burnout. Annals of Family Medicine. 17 (6),
487-494. Available at: https://doi.org/10.1370/afm.2470.
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Ultimately, we are focused on supporting effective and sustainable
collaboration between healthcare delivery and local community-based
services organizations to meet the unmet needs of people they serve.
Reporting data from both the Screening for Social Drivers of Health and
the Screen Positive Rate for Social Drivers of Health measures will
enable both identification and quantification of the levels of unmet
HRSNs among communities served by IPFs. These two Social Drivers of
Health measures harmonize, as it is important to know both whether
screening occurred and the results from the screening in order to
develop sustainable solutions. We believe that there are multiple
benefits to increasing IPFs' understanding of their patients' HRSNs.
First, we believe that this could lead to increased clinical-community
collaborations and an associated increase in system capacity and
community investments. Second, we believe this in turn could yield a
net reduction in costly healthcare utilization by promoting more
appropriate healthcare service consumption.\171\
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\171\ Centers for Medicare & Medicaid Services. (2021).
Accountable Health Communities Model. Accountable Health Communities
Model [verbar] CMS Innovation Center. Available at: https://innovation.cms.gov/innovation-models/ahcm. Accessed November 23,
2021.
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Pursuant to our Meaningful Measures 2.0 Framework and in alignment
with the measures previously adopted for hospitals participating in the
Hospital IQR Program, the Screen Positive Rate for Social Drivers of
Health measure will address the equity priority area and align with our
commitment to introduce plans to close health equity gaps and promote
equity through quality measures, including to ``develop and implement
measures that reflect social and economic determinants.'' \172\ Under
our Meaningful Measures Framework, the Screen Positive Rate for Social
Drivers of Health measure will address the quality priority of ``Work
with Communities to Promote Best Practices of Healthy Living'' through
the Meaningful Measures Area of ``Equity of Care.'' \173\ Adoption of
this measure will also align with our strategic pillar to advance
health equity by addressing the health disparities that underlie our
health system.\174\
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\172\ Centers for Medicare & Medicaid Services. Meaningful
Measures 2.0: Moving from Measure Reduction to Modernization.
Available at: https://www.cms.gov/meaningful-measures-20-moving-measure-reduction-modernization.
\173\ Centers for Medicare & Medicaid Services. (2021). CMS
Measures Management System Blueprint (Blueprint v 17.0). Available
at: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/MMS/MMS-Blueprint.
\174\ Brooks-LaSure, C. (2021). My First 100 Days and Where We
Go From Here: A Strategic Vision for CMS. Available at: https://www.cms.gov/blog/my-first-100-days-and-where-we-go-here-strategic-vision-cms.
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b. Overview of Measure
The Screen Positive Rate for Social Drivers of Health measure is
intended to enhance standardized data collection that can identify
individuals who are at higher risk for poor health outcomes related to
HRSNs who would benefit from connection via the IPF to targeted
community-based services.\175\ The measure identifies the proportion of
patients admitted to an IPF stay who are 18 years or older on the date
of admission to the IPF who screened positive for one or more of the
following five HRSNs: food insecurity, housing instability,
transportation needs, utility difficulties, and interpersonal safety.
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\175\ Centers for Medicare & Medicaid Services. (2021). A Guide
to Using the Accountable Health Communities Health-Related Social
Needs Screening Tool: Promising Practices and Key Insights (June
2021). Available at: https://innovation.cms.gov/media/document/ahcm-screeningtool-companion. Accessed November 23, 2021.
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Consistent with the Hospital IQR Program, which adopted this
measure in the FY 2023 IPPS/LTCH PPS final rule (87 FR 49215 through
49220), we will require IPFs to report this measure as five separate
rates. Specifically, IPFs will report the number of patients who
screened positive for food insecurity, the number of patients who
screened positive for housing instability, the number of patients who
screened positive for transportation needs, the number of patients who
screened positive for utility difficulties, and the number of patients
who screened positive for interpersonal safety. We note that this
measure is intended to provide information to IPFs on the level of
unmet HRSNs among patients served, and not for comparison between IPFs.
The specifications for the Screen Positive Rate for Social Drivers
of Health measure, which were available during the review of the MUC
List, are available at: https://mmshub.cms.gov/sites/default/files/map-hospital-measure-specifications-manual-2022.pdf.
(1) Measure Calculation
(a) Cohort
The Screen Positive Rate for Social Drivers of Health measure is a
process measure that provides information on the percent of patients,
18 years or older on the date of admission for an IPF stay, who were
screened for all five HRSNs,\176\ and who screen positive for one or
more of the following five HRSNs: food insecurity; housing instability;
transportation needs; utility difficulties; or interpersonal safety.
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\176\ We have updated this language to read ``all five HRSNs''
as opposed to ``an HRSN'' to update the language on the 2022 MUC
List: https://mmshub.cms.gov/sites/default/files/2022-MUC-List.xlsx.
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(b) Numerator
The numerator consists of the number of patients admitted for an
IPF stay who are 18 years or older on the date of admission, who were
screened for an HRSN, and who screen positive for having an unmet need
in one or more of the following five HRSNs (calculated separately): The
number of patients who screened positive for food insecurity, the
number of patients who screened positive for housing instability, the
number of patients who screened positive for transportation needs, the
[[Page 51119]]
number of patients who screened positive for utility difficulties, and
the number of patients who screened positive for interpersonal safety.
IPFs will report the number of patients who screened positive for
having unmet needs in each of the five HRSNs as a separate numerator. A
patient who screened positive for more than one unmet HRSN will be
included in the numerator for each of those HRSNs. For example, a
patient who screened positive for food insecurity, housing instability,
and transportation needs would be included in each of these numerators.
(c) Denominator
The denominator consists of the number of patients admitted for an
IPF stay who are 18 years or older on the date of admission and are
screened for all five HRSNs (food insecurity, housing instability,
transportation needs, utility difficulties and interpersonal safety)
\177\ during their IPF stay. The following patients are excluded from
the denominator: (1) patients who opt out of screening; and (2)
patients who are themselves unable to complete the screening during
their inpatient stay and have no caregiver able to do so on the
patient's behalf during their inpatient stay.
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\177\ We have updated this language to read ``all five HRSNs''
as opposed to ``an HRSN'' to update the language on the 2022 MUC
List: https://mmshub.cms.gov/sites/default/files/2022-MUC-List.xlsx.
---------------------------------------------------------------------------
(d) Calculation
The results of this measure are calculated as five separate rates.
Each rate is derived from the number of patients admitted for an IPF
stay and who are 18 years or older on the date of admission, screened
for an HRSN, and who screen positive for each of the five HRSNs (that
is, the number of patients who screened positive for food insecurity,
the number of patients who screened positive for housing instability,
the number of patients who screened positive for transportation needs,
the number of patients who screened positive for utility difficulties,
and the number of patients who screened positive for interpersonal
safety) divided by the number of patients 18 years or older on the date
of admission screened for all five HRSNs. The measure is reported as
five separate rates--one for each HRSN, each calculated with the same
denominator.
(2) Review by the Measure Applications Partnership
We included the Screen Positive Rate for Social Drivers of Health
measure on the publicly available MUC List, a list of measures under
consideration for use in various Medicare programs.\178\ The CBE-
convened MAP Health Equity Advisory Group reviewed the MUC List and the
Screen Positive Rate for Social Drivers of Health measure (MUC 2022-
050) in detail on December 6 through 7, 2022.\179\ The MAP Health
Equity Advisory Group expressed support for the collection of data
related to social drivers of health, but raised concerns regarding
public reporting of these data and potential repetition of asking
patients the same questions across settings.\180\
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\178\ Centers for Medicare & Medicaid Services. List of Measures
Under Consideration for December 1, 2022. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\179\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\180\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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In addition, on December 8 through 9, 2022, the MAP Rural Health
Advisory Group reviewed the 2022 MUC List, which was also reviewed by
the MAP Hospital Workgroup on December 13 through 14, 2022.\181\ The
MAP Rural Health Advisory Group noted potential reporting challenges
including the potential masking of health disparities that are
underrepresented in some areas and that sample size and populations
served may be an issue but also expressed support that the measure
seeks to advance the drivers of health and serves as a starting point
to determine where screening is occurring. The MAP Hospital Workgroup
recommended conditional support of the measure for rulemaking pending:
(1) endorsement by the CBE to address reliability and validity
concerns; (2) attentiveness to how results are shared and
contextualized for public reporting; and (3) examination of any
differences in reported rates by reporting process (that is, to assess
whether reported rates are the same or different across IPFs and other
facilities that may use different processes to report their data).\182\
Thereafter, the MAP Coordinating Committee deliberated on January 24
through 25, 2023, and ultimately voted to conditionally support the
Screen Positive Rate for Social Drivers of Health measure for
rulemaking with the same conditions.\183\
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\181\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\182\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\183\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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We agree with the MAP Coordinating Committee's support for the
proposed Screen Positive Rate for Social Drivers of Health measure. We
believe this measure, alongside the Screening for Social Drivers of
Health measure, establishes an important foundation to prioritizing the
achievement of health equity among IPFs participating in the IPFQR
Program. Our approach to developing health equity measures is
incremental, and we believe that health equity outcomes in the IPFQR
Program will inform future efforts to advance and achieve health equity
by IPFs. We believe this measure to be a building block that lays the
groundwork for a future meaningful suite of measures that would assess
IPF progress in providing high-quality healthcare for all patients,
regardless of social risk factors or demographic characteristics.
(3) CBE Endorsement
We have not submitted this measure for CBE endorsement at this
time. Although section 1886(s)(4)(D)(i) of the Act generally requires
that measures specified by the Secretary must be endorsed by the entity
with a contract under section 1890(a) of the Act, section
1886(s)(4)(D)(ii) of the Act states that in the case of a specified
area or medical topic determined appropriate by the Secretary for which
a feasible and practical measure has not been endorsed by the entity
with a contract under section 1890(a) of the Act, the Secretary may
specify a measure that is not so endorsed as long as due consideration
is given to a measure that has been endorsed or adopted by a consensus
organization identified by the Secretary. We reviewed measures endorsed
by consensus organizations and were unable to identify any other
measures on this topic endorsed by a consensus organization; therefore,
we believe the exception in section 1886(s)(4)(D)(ii) of the Act
applies.
c. Data Collection, Submission, and Reporting
We believe incremental implementation of the Screen Positive Rate
for Social Drivers of Health measure, by permitting one year of
voluntary reporting prior to mandatory reporting, will allow IPFs who
are not
[[Page 51120]]
yet screening patients for HRSNs to get experience with the measure and
equally allow IPFs who already undertake screening efforts to report
data already being collected. Therefore, we proposed voluntary
reporting of this measure, along with the Screening for Social Drivers
of Health measure described in section VI.D.3 of this final rule,
beginning with the data collected in CY 2024, which will be reported to
CMS in CY 2025 followed by mandatory reporting beginning with data
collected in CY 2025, which will be reported to CMS in CY 2026 and
affect FY 2027 payment determination.
While this measure will require IPFs to collect patient-level data
on their patients' social drivers of health screening results, we
proposed to adopt this measure as an aggregate measure (that is, IPFs
would be required to submit only numerator results for each of the five
screening areas and the number of patients screened for all five of the
HRSNs). IPFs are required to submit information for aggregate chart-
abstracted measures once annually using a CMS-approved web-based data
collection tool available within the HQR System (previously referred to
as the QualityNet Secure Portal). We refer readers to section VI.I of
this final rule (Form, Manner, and Timing of Quality Data Submission)
for more details on our previously finalized data submission and
deadline requirements across measure types.
We invited public comment on our proposal.
We note that we have addressed comments that broadly referred to
both the Screening for Social Drivers of Health measure and the Screen
Positive Rate for Social Drivers of Health measure in the previous
section of this final rule (VI.D.3.).
Comment: Many commenters supported adoption of the Screen Positive
Rate for Social Drivers of Health measure. Some commenters stated that
knowing which patients have each of these HRSNs will help IPFs better
understand patients' needs, improve care coordination with outpatient
and community resources, increase the dignity and respect with which
patients are treated, and support development of patient-centered
treatment plans.
Response: We thank commenters for their support of the Screen
Positive Rate for Social Drivers of Health measure. We agree that HRSNs
are critical factors that impact patient outcomes, and increased
knowledge about patients' HRSNs will help IPFs shape goals associated
with health equity. Further, we agree that collecting these data will
help IPFs improve coordination with outpatient and community resources
to better deliver patient-centered care.
Comment: One commenter stated that access to these data will be
useful for patient advocates to be able to identify IPFs that are more
experienced with treating patients with more intensive resource needs.
Response: We agree with the commenter that publicly reporting these
data might help patients with more intensive resource needs select IPFs
that are more familiar with treating patients with that level of need.
We note, however, that the measure is intended to provide information
to IPFs on the level of unmet need among their patients and potentially
in the community, and not for comparison between IPFs (88 FR 21286).
Comment: Some commenters expressed concern that publicly reporting
these data may lead to inaccurate perceptions of the quality of care at
IPFs that treat high volumes of patients who screen positive for one or
more HRSNs. Several of these commenters stated that IPF patients may
also have more unmet HRSNs than those at acute care hospitals so the
data may be further misleading if the two settings are compared.
Response: We appreciate the commenters' concerns. The measure is
intended to provide information to IPFs on the level of unmet need
among their patients and potentially in the community, and not for
comparison between IPFs (88 FR 21286). We believe public reporting of
healthcare quality data promotes transparency in the delivery of care
by increasing the involvement of leadership in healthcare quality
improvement, creating a sense of accountability, helping to focus
organizational priorities, and providing a means of delivering
important healthcare information to consumers and patient advocates. We
intend to conduct outreach and education with providers and patients to
share information about the two Social Drivers of Health measures in
conjunction with public reporting.
Comment: One commenter expressed the belief that reporting five
separate rates, individually reflecting the proportion of patients who
screened positive for each of the five HRSNs, is a flawed methodology
because it may not yield reliable and valid comparisons. Another
commenter expressly supported reporting five separate rates for this
measure to improve transparency.
Response: We believe that reporting a separate screen positive rate
for each of the five HRSNs will provide important information to IPFs,
the communities that they serve, and policy makers. Because different
community-based resources are appropriate to address each of the five
HRSNs, we believe that reporting each of these rates separately will
provide reliable and valid information to identify which communities
are most in need of which resources to better enable support in
addressing the most prevalent HRSNs.
Comment: Several commenters recommended that we develop outcome
measures related to each of the five HRSNs for future adoption in this
and other quality reporting programs.
Response: We thank commenters for their feedback. We view the two
Social Drivers of Health measures as a first step towards development
of a long-term strategy to integrate social drivers of health data into
IPF quality performance measurement as part of our broader commitment
to health equity. We will continue to take all comments, concerns, and
suggestions into account and will consider them as part of any
potential new measure development in future notice-and-comment
rulemaking.
Comment: One commenter requested clarification on how to define a
positive screening on a tool with a reporting scale.
Response: Because the reported value of screening results could
vary among different screening tools or instruments, we recommend that
IPFs carefully review the supporting materials that accompany each tool
to understand how to properly administer the instrument and interpret
results when selecting a screening instrument for their patient
population.
Comment: One commenter did not support adoption of the Screen
Positive Rate for Social Drivers of Health measure because the
commenter expressed their belief that only IPFs would be able to use
the data regarding their patient population and that they will already
have the data from performing the screening.
Response: We respectfully disagree and believe that there are
multiple interested parties who will be able to use data regarding
IPFs' patient populations, including patients and their caregivers,
patient advocacy organizations, local community services organizations,
and federal, state, and local policy makers. We also believe that the
measure will facilitate systematic gathering of such data in a manner
that provides information to IPFs on the level of unmet need among
their patients that many IPFs do not compile currently.
Final Decision: After consideration of the public comments we
received, we
[[Page 51121]]
are finalizing adoption of the Screen Positive Rate for Social Drivers
of Health measure as proposed.
5. Adoption of the Psychiatric Inpatient Experience (PIX) Survey
Beginning With Voluntary Reporting of CY 2025 Data Followed by
Mandatory Reporting Beginning With CY 2026 Data/FY 2028 Payment
Determination
a. Background
We believe that a comprehensive approach to quality must include
directly reported feedback regarding facility, provider, and payer
performance. Therefore, we have consistently stated our commitment to
identifying an appropriate patient experience of care measure for the
IPF setting and adopting this measure in the IPFQR Program at the first
opportunity (77 FR 53646, 78 FR 50897, 79 FR 45964 through 45965, 80 FR
46714 through 46715, 82 FR 38470 through 38471, 83 FR 38596, 84 FR
38467, 85 FR 47043, 86 FR 42654 through 42656, and 87 FR 46846).
In the FY 2014 IPPS/LTCH PPS final rule, we adopted a voluntary
information collection regarding whether IPFs participating in the
IPFQR Program assess patient experience of inpatient behavioral health
services using a standardized instrument and for IPFs that answer
``Yes'' to indicate the name of the survey that they administer (78 FR
50896 through 50897). In the FY 2015 IPF PPS final rule, we adopted
this information collection as the Assessment of Patient Experience of
Care measure beginning with the FY 2016 payment determination (79 FR
45964 through 45965). Data collected for the FY 2018 payment
determination (that is, data collected in CY 2016) showed that while
the majority of IPFs (approximately 76 percent) were collecting patient
experience of care data through a standardized instrument, there was a
wide variation in the instrument being used. The data for CY 2016
indicated that the most widely used survey instrument was not in the
public domain and was used by less than 30 percent of the IPFs that
used a patient experience survey. In the FY 2015 IPF PPS final rule, we
indicated our intention to adopt a standardized measure of patient
experience of care for the IPFQR Program (79 FR 45964 through 45965).
In the FY 2019 IPF PPS final rule, we removed the Assessment of
Patient Experience of Care measure from the IPFQR Program, because we
believed that we had collected sufficient information to inform
development of a patient experience of care measure (83 FR 38596
through 38597). In the FY 2020 IPF PPS final rule, we summarized our
analysis of the results of the Assessment of Patient Experience of Care
measure and requested feedback on potential adoption of the Hospital
Consumer Assessment of Healthcare Providers and Systems (HCAHPS) survey
for the IPFQR Program (84 FR 38467). In response to our request, many
commenters expressed concern that the HCAHPS survey was not specified
for the IPF setting and recommended that CMS identify a survey that has
been developed for and tested in the IPF setting. Furthermore, in the
FY 2021 IPF PPS proposed rule, we did not propose any updates to the
IPFQR Program; however, we received many comments requesting that we
adopt a patient experience of care measure in the IPFQR Program, which
we summarized in the FY 2021 IPF PPS final rule (85 FR 47043). We
received similar input strongly advocating for a patient experience of
care measure for the IPFQR Program in response to a solicitation of
comments on potential measures for the IPFQR Program in the FY 2022 IPF
PPS proposed rule (86 FR 19511 through 19512), which we summarized in
the FY 2022 IPF PPS final rule (86 FR 42654 through 42656). Many of
these comments were from patients and their families and described how
meaningful such a measure would be for individuals who receive services
from IPFs. Though we did not solicit input on a patient experience of
care measure in the FY 2023 IPF PPS proposed rule, we received many
comments strongly recommending that we adopt such a measure, which we
summarized in the FY 2023 IPF PPS final rule (87 FR 46846). Since
publication of the FY 2023 IPF PPS final rule, section 4125(c) of the
Consolidated Appropriations Act, 2023 (Pub. L. 117-328) was enacted,
which amends section 1886(s)(4) of the Act to require that the quality
measures specified for the IPFQR Program must include a quality measure
of patients' perspective on care not later than the FY 2031 payment
determination.
We have continued to review publicly available patient experience
of care instruments to identify such an instrument specified for, and
tested in, the IPF setting. In our review, we identified the
Psychiatric Inpatient Experience (PIX) survey as a publicly available
survey instrument developed for and tested in the IPF setting. Pursuant
to the Meaningful Measures 2.0 Framework, this measure addresses the
``Person-Centered'' priority area, as well as the ``Individual and
Caregiver Voice'' foundation and aligns with our commitment to
prioritize outcome and patient-reported measures.\184\ This measure
also aligns with the CMS National Quality Strategy Goal 4 ``Foster
Engagement.'' It also supports the Behavioral Health Strategy goal of
``Strengthen Equity and Quality in Behavioral Health Care.'' \185\
Furthermore, this measure supports the new Universal Foundation domain
of ``Person-Centered Care.'' \186\
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\184\ Centers for Medicare & Medicaid Services. Meaningful
Measures 2.0: Moving from Measure Reduction to Modernization.
Available at: https://www.cms.gov/meaningful-measures-20-moving-measure-reduction-modernization.
\185\ CMS. (2022). CMS Behavioral Health Strategy. Available at
https://www.cms.gov/cms-behavioral-health-strategy. Accessed on
February 20, 2023.
\186\ https://www.nejm.org/doi/full/10.1056/NEJMp2215539.
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b. Overview of Measure
The PIX survey was developed by a team at the Yale University, Yale
New Haven Psychiatric Hospital to address the gap in available
experience of care surveys, specifically the lack of publicly
available, minimally burdensome, psychometrically validated surveys
specified for the IPF setting.\187\ The interdisciplinary team that
developed this survey, including researchers and clinicians, conducted
the following steps in developing the survey: (1) literature review;
(2) patient focus groups; (3) solicitation of input from a patient and
family advisory council; (4) review of content validity with an expert
panel; (5) development of survey; and (6) survey testing within the
Yale New Haven Psychiatric Hospital system.\188\
---------------------------------------------------------------------------
\187\ Klemanski DH, Barnes T, Bautista C, Tancreti C, Klink B,
Dix E. Development and Validation of the Psychiatric Inpatient
Experience (PIX) Survey: A Novel Measure of Patient Experience
Quality Improvement. Journal of Patient Experience. 2022;9.
doi:10.1177/23743735221105671
\188\ Klemanski DH, Barnes T, Bautista C, Tancreti C, Klink B,
Dix E. Development and Validation of the Psychiatric Inpatient
Experience (PIX) Survey: A Novel Measure of Patient Experience
Quality Improvement. Journal of Patient Experience. 2022;9.
doi:10.1177/23743735221105671.
---------------------------------------------------------------------------
The resulting survey contains 23 items in four domains. Patients
can respond to each of the 23 items using a five-point Likert scale
(that is, strongly disagree, somewhat disagree, neutral, somewhat
agree, strongly agree) or choose that the item does not apply. The four
domains are:
Relationship with Treatment Team;
Nursing Presence;
Treatment Effectiveness; and
Healing Environment.\189\
---------------------------------------------------------------------------
\189\ Klemanski DH, Barnes T, Bautista C, Tancreti C, Klink B,
Dix E. Development and Validation of the Psychiatric Inpatient
Experience (PIX) Survey: A Novel Measure of Patient Experience
Quality Improvement. Journal of Patient Experience. 2022;9.
doi:10.1177/23743735221105671.
---------------------------------------------------------------------------
[[Page 51122]]
The PIX survey is distributed to patients by administrative staff
at a time beginning 24 hours prior to planned discharge. The survey,
which is available in both English and Spanish and in accessible
formats can be completed prior to discharge using either a paper copy
of the survey or an electronic version of the survey via tablet
computer.\190\ For a complete list of survey questions, including which
questions are elements of each domain, we refer readers to the
description of the survey in the Journal of Patient Experience: .
---------------------------------------------------------------------------
\190\ Klemanski DH, Barnes T, Bautista C, Tancreti C, Klink B,
Dix E. Development and Validation of the Psychiatric Inpatient
Experience (PIX) Survey: A Novel Measure of Patient Experience
Quality Improvement. Journal of Patient Experience. 2022;9.
doi:10.1177/23743735221105671.
---------------------------------------------------------------------------
(1) Measure Calculation
(a) Cohort
The cohort for this measure is all patients discharged from an IPF
during the reporting period who do not meet one of the following
exclusions: (1) patients who are under 13 years of age at time of
discharge, and (2) patients who are unable to complete the survey due
to cognitive or intellectual limitations. The sampling procedures that
IPFs can apply to the PIX survey measure are described in section
VI.I.6 of this final rule.
(b) Calculation
The measure will be reported as five separate rates, one for each
of the four domains of the PIX survey and one overall rate. Each of
these rates will be calculated from patient responses on the PIX survey
and then publicly reported on the Care Compare website (or successor
CMS website). We will report the mean rates for each domain as well as
the overall mean rate on the Care Compare website (or successor CMS
website). To calculate the mean scores, we will assign a numerical
value ranging from 1 (Strongly Disagree) to 5 (Strongly Agree). We will
then calculate the average response by adding the values of all
responses and dividing that value by the number of responses, excluding
questions that were omitted or to which the patient selected ``Does Not
Apply.''
(2) Review by the Measure Applications Partnership (MAP)
We included the PIX survey measure on the publicly available ``List
of Measures Under Consideration for December 1, 2022'' (MUC List), a
list of measures under consideration for use in various Medicare
programs.\191\ The CBE-convened Measure Applications Partnership (MAP)
reviewed the MUC List and discussed the potential use of the PIX survey
for the IPFQR Program.
---------------------------------------------------------------------------
\191\ Centers for Medicare & Medicaid Services. List of Measures
Under Consideration for December 1, 2022. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
---------------------------------------------------------------------------
The MAP Health Equity Advisory Group agreed that well-constructed
patient experience of care measures are an important indicator of
quality care. Overall, the MAP Health Equity Advisory Group expressed
that this measure is a ``step in the right direction for behavioral
health.'' \192\
---------------------------------------------------------------------------
\192\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
---------------------------------------------------------------------------
In addition, on December 8 through 9, 2022, the MAP Rural Health
Workgroup reviewed the 2022 MUC List and expressed support for this
measure, with patient support being especially strong. Some members of
the MAP Rural Health Advisory Group were concerned about operational
challenges, specifically costs related to implementation and
maintenance and potential bias if the surveying occurs prior to
discharge.\193\
---------------------------------------------------------------------------
\193\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
---------------------------------------------------------------------------
The MAP Hospital workgroup reviewed the 2022 MUC List on December
13 through 14, 2022. The MAP Hospital workgroup conditionally supported
the measure for rulemaking, while emphasizing the importance of
including patient reported experience of care data in the IPFQR
Program. The MAP Hospital workgroup's conditions for support included
endorsement by the CBE and additional testing data for this measure,
specifically: (1) data from testing of the measure in a variety of
settings (including urban, rural, safety net providers, and others),
(2) data regarding survey results depending on the timing of survey
administration (pre- versus post-discharge), (3) data regarding patient
factors (for example, voluntary versus involuntary admissions), and (4)
data regarding of mode of administration (for example, email versus
mail) that may affect performance.\194\ Thereafter, the MAP
Coordinating Committee deliberated on January 24 through 25, 2023 and
ultimately voted to uphold the Hospital Workgroup's recommendation to
conditionally support the PIX survey measure for rulemaking pending the
same conditions as the MAP Hospital workgroup.\195\
---------------------------------------------------------------------------
\194\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\195\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
---------------------------------------------------------------------------
We believe that the testing that has been conducted on the PIX
survey demonstrates that it is a valid and reliable tool for measuring
patient experience of care in IPFs, and that the results from this
initial testing are generalizable across IPFs. However, we agree with
the MAP Hospital workgroup that additional testing of this measure
could help better understand measure results, including any differences
in measure results that were not analyzed during the PIX survey's
initial testing. Therefore, the measure developer intends to conduct
additional testing of the PIX survey prior to public reporting of the
measure data, and we proposed a voluntary reporting period before
beginning mandatory reporting of the PIX survey.\196\
---------------------------------------------------------------------------
\196\ We note that in the FY 2024 IPF PPS proposed rule we
inadvertently stated in section V.5.b.(2) ``Review by the MAP'' of
the proposal that we were providing a two-year voluntary reporting
period (88 FR 21289), which was inconsistent with our proposal to
provide a one-year voluntary reporting period (88 FR 21290). As
noted throughout the proposed rule, we proposed that voluntary
reporting would begin with CY 2025 data and mandatory reporting
would begin with CY 2026 data. We have corrected the above error
here.
---------------------------------------------------------------------------
(3) CBE Endorsement
The measure developer has not submitted this measure for CBE
endorsement at this time. The developer does intend to submit this
measure for endorsement in the future, following additional testing as
recommended by the MAP Hospital workgroup. Although section
1886(s)(4)(D)(i) of the Act generally requires that measures specified
by the Secretary must be endorsed by the entity with a contract under
section 1890(a) of the Act, section 1886(s)(4)(D)(ii) of the Act states
that in the case of a specified area or medical topic determined
appropriate by the Secretary for which a feasible and practical measure
has not been endorsed by the entity with a contract under section
1890(a) of the Act, the Secretary may specify a measure that is not so
endorsed as long as due consideration is given to a measure that has
been endorsed or adopted by a consensus organization identified by the
Secretary.
We reviewed measures endorsed by consensus organizations and were
[[Page 51123]]
unable to identify any other measures on this topic endorsed by a
consensus organization. We did identify the Experience of Care and
Health Outcomes (ECHO) Survey measure (CBE #008); however, this measure
has had its endorsement removed as of the spring 2020 cycle.
Additionally, the ECHO Survey was developed and tested for outpatient
behavioral health, not the inpatient setting. Additionally, we
identified the Patient Experience of Psychiatric Care as Measured by
the Inpatient Consumer Survey (ICS) measure (CBE #0726). This measure
has also had its endorsement removed as of the spring 2018 cycle. As
neither of these two measures is endorsed at this time, we believe the
exception in section 1886(s)(4)(D)(ii) of the Act applies.
c Data Collection, Submission and Reporting
IPFs will be responsible for administering the survey and
collecting data on survey responses, because the PIX survey is
administered beginning 24 hours prior to a patient's planned discharge.
Therefore, IPFs will collect the data in a manner similar to the
collection of data for chart-abstracted measures or other patient
screening measures. That is, the IPFs will collect data in the facility
and then report these data to CMS using the methods described in
section VI.I.4 of this final rule, ``Data Submission Requirements,''
under ``Procedural Requirements.''
Because we anticipate that many IPFs, which already administer
different patient experience of care survey instruments to their
patients, will need to transition to the PIX survey, we proposed a
voluntary reporting period beginning with data from CY 2025, which will
be reported to CMS in CY 2026. We will then require IPFs to report data
for the PIX survey measure beginning with data collected during CY
2026, to be reported to CMS during CY 2027 and affecting the FY 2028
payment determination.
We invited comments on our proposal.
Comment: Many commenters strongly supported the PIX survey measure.
These commenters expressed that the measure addresses a long-standing
measure gap in the IPFQR Program, which these commenters characterized
as discriminatory, and specifically supported the PIX survey instrument
because it was developed with input from people with lived experience
in the IPF setting. Some of these commenters representing patients and
their families provided descriptions of their own and their family
members' lived experiences to explain how important such a survey
opportunity would be to IPF patients. Some commenters stated that
patients are especially vulnerable during inpatient treatment and that
psychological distress can be exacerbated in this setting. These
commenters expressed that collecting data regarding the patients'
experiences of care can improve patient-centered, trauma-informed care
in which patients are treated with dignity and respect. Other
commenters stated that formal patient feedback motivates improved care.
One commenter stated that collection and public reporting of these data
would assist community-based providers in identifying IPFs to which to
refer patients. Other commenters stated that surveying IPF patients
regarding their experience of care is a form of treating them with
dignity and respect, empowering them, and showing that their
experiences are important. Several commenters stated that survey data
can be tied to other data sets to support research. Another commenter
expressed that IPFs will be able to compare themselves to other IPFs,
which could motivate quality improvement.
Response: We thank commenters for their support of the PIX survey
measure. We agree that adoption of a patient experience of care measure
for the IPF setting addresses a long-standing measure gap, encourages
patient-centered care, and shows that we believe that the patient's
experience is a critical element of providing quality care.
Comment: Some commenters expressed concern regarding measuring
patient experience of care prior to discharge. Some of these commenters
expressed that patients may feel unsafe responding honestly at any
point prior to discharge because of a fear of retaliation for
unfavorable responses. These commenters recommended providing an option
for patients to respond post-discharge (such as providing a paper copy
of the survey with a sealable, addressed envelope to return the survey
after completing it). Another commenter stated that the setting in
which the survey is administered, and time provided to complete the
survey, could lead to variation in results and recommended
administering the survey post-discharge. Many commenters recommended
allowing vendors to collect and report the data for IPFs. Other
commenters were specifically concerned regarding the 24 hours prior to
discharge time period for administering the survey. Some of these
commenters stated that there are many clinical activities occurring
during this phase of the patient's stay and that adding another step
may be burdensome for staff and patients. Other commenters concerned
about the 24 hour prior to discharge time period expressed that
discharge timelines are often uncertain, and therefore it may be
difficult to know when the 24 hours prior to discharge window has
started, especially for patients with long stays.
Response: We would like to clarify that, if it is not possible for
a patient to complete the survey prior to discharge, the facility
should provide a sealable, addressed envelope for the patient to return
the survey following discharge. This situation could apply in
situations in which the patient would prefer more time or privacy to
complete the survey, in situations in which there are competing
clinical priorities prior to discharge, or in situations in which there
is uncertainty regarding the timing of a patient's discharge. However,
we caution IPFs that relying exclusively on the mail-back option may
prevent the IPF from meeting the measure's minimum sampling
requirements. If the IPF is able to meet the minimum sampling
requirements and chooses to use a vendor to receive paper surveys,
aggregate and analyze data provided through the surveys, or to report
these data to CMS on the IPF's behalf, that would be consistent with
the measure methodology and specifications.
Comment: Many commenters expressed support for surveying patients
regarding their experience of care, but expressed that they already
have tools or vendors in place and that transitioning to the PIX survey
would be disruptive. Some commenters specifically stated that this
transition would disrupt their historical trend data. One commenter
expressed concern that patients complete too many experience surveys
and recommended that CMS select one tool based on an evaluation of all
current surveys. Some commenters expressed a preference for a CAHPS
survey because these surveys are used in other care settings and are
the core element of the CMS Foundational Measurement Strategy to
address the person-centered care domain. Other commenters stated that
patients with primary psychiatric diagnoses continue to be excluded
from HCAHPS and that, even if this exclusion were removed, by adopting
the PIX survey, data about patient experience in an IPF would not be
comparable to data regarding patient experience in general acute care
hospitals. Other commenters recommended that CMS allow IPFs to select
their own patient experience instrument provided that it addresses
[[Page 51124]]
the domains addressed by the PIX survey.
Response: We recognize that many IPFs already use patient
experience of care survey instruments or vendors to administer and
collect survey instruments on behalf of IPFs, and that there is a
burden for these IPFs to transition to a new survey instrument and
administration and collection process. We further recognize that
historical quality improvement trend data and analytical processes may
be impacted for these IPFs who already use other patient experience of
care survey instruments. We considered allowing IPFs to select their
own patient experience data collection instrument provided that it
addresses the domains addressed by the PIX survey. However, we believe
that using a single, standardized instrument to assess patient
experience of care across both freestanding IPFs and those psychiatric
units in acute care hospitals will provide comparability of experience
data. We believe that publicly reporting patient experience of care
data that allows for comparisons between IPFs will be most meaningful
to patients and their caregivers, and will allow IPFs to compare their
measure results to similar IPFs as part of their quality improvement
initiative. We understand commenters' concern that by adopting a
different patient experience of care measure in the IPF setting than
that for general acute care hospitals (that is, the HCAHPS survey)
measure results will not be comparable across these settings, even if
HCAHPS is expanded to patients with primary psychiatric diagnoses in
the general acute care setting. However, in response to our previous
RFIs about incorporating a patient experience of care measure in the
IPFQR Program, many commenters (representing patients, patient
advocates, caregivers, IPFs, and provider associations) recommended
that we adopt a patient experience of care measure that was developed
specifically for patients receiving care in IPFs (84 FR 38467). These
commenters stated that there are elements of care, such as group
therapy, that are unique to the IPF setting and stated that a survey
for this setting should specifically address these elements of care.
Because it was developed specifically for this setting, with input from
patients and their caregivers, the PIX survey does include questions
regarding these unique elements of care, whereas the HCAHPS survey does
not.
With respect to concerns regarding loss of trend data, we have
proposed to adopt the measure for mandatory reporting beginning with CY
2026 data (which will be submitted to CMS in CY 2027 and affect FY 2028
payment determination) to provide additional time for IPFs to
transition to this new survey. We wish to clarify that IPFs will be
permitted to add questions to the survey, so if there are specific
metrics that an IPF wishes to continue tracking, they will be able to
do so. We believe that IPFs will have sufficient time prior to when
mandatory reporting of this measure begins with the FY 2028 payment
determination to determine which questions will be most appropriate to
add to the survey without overburdening patients, or how to compare
results from patient responses to the PIX survey to those of their
existing surveys.
We believe that the commenter who referenced the CMS Foundational
Measurement Strategy was referring to the CMS Universal
Foundation,\197\ which includes setting specific versions of the
Consumer Assessment of Healthcare Providers and Systems (CAHPS) survey.
We considered potential adoption of a CAHPS measure for the IPFQR
Program and solicited comment on this in the FY 2020 IPF PPS proposed
rule (84 FR 16986 through 16987) and summarized the responses to this
request in the FY 2020 IPF PPS final rule (84 FR 38467). Following our
review of the HCAHPS survey and responses to that request for
information, we determined that the PIX survey is more appropriate for
the IPFQR Program since it has been developed and tested specifically
for IPFs and with the input of individuals with lived experience with
care in this setting. Therefore, while the HCAHPS survey is appropriate
for the general acute care setting, we believe that the PIX survey is a
more appropriate instrument for measuring patient experience of care in
the IPF setting.
---------------------------------------------------------------------------
\197\ https://www.cms.gov/aligning-quality-measures-across-cms-universal-foundation.
---------------------------------------------------------------------------
Comment: Many commenters expressed concern that the PIX survey has
not been sufficiently tested for national implementation. These
commenters specifically noted a lack of testing in diverse geographic
settings (including testing for differences in performance in urban
versus rural settings), lack of testing which compares this survey to
other inpatient consumer surveys, lack of information about the
correlation coefficients for the proposed domains, lack of reliability
coefficients to determine the survey's internal consistency, lack of
demographic data regarding patients who respond versus those who do
not, lack of testing among the forensically and/or involuntarily
admitted populations, lack of longitudinal testing, and lack of testing
with facilities which have an average length of stay greater than 10
days. Some commenters recommended additional testing with volunteer
IPFs prior to implementation as a mandatory measure. Some of these
commenters recommended postponing mandatory adoption to ensure
sufficient testing. One commenter expressed concern that the PIX survey
does not clearly connect questions to key outcomes, and recommended
further research and testing to identify these connections.
Response: We understand commenters' concerns regarding the testing
of the PIX survey measure. We recognize that this is a relatively new
instrument. We note that the measure developer is continuing to test
this instrument to further address these questions and concerns prior
to the national implementation of the measure. To increase time for
testing and to better identify information that will need to be
provided during education and outreach sessions prior to public
reporting, we proposed and are adopting mandatory reporting of this
measure for the FY 2028 payment determination, which would not require
IPFs to begin administering and collecting responses to the PIX survey
until CY 2026.
Comment: Some commenters expressed concern that this survey
instrument is only available in a limited number of languages and
recommended translation into additional languages to improve
accessibility for all patients. Some of these commenters recommended
adding supportive services to help those with language barriers or
limited health literacy complete the survey.
Response: The measure developer has translated the survey from
English into Spanish, Mandarin, and Farsi. The measure developer is
currently working to translate the survey into other frequently
requested languages (including, French, Arabic, and Japanese). For
patients who have language barriers, the measure developer is currently
developing survey administration guidelines for best practices in
survey administration to enhance the accessibility of the PIX survey.
These include but are not limited to screen readers, the use of visual
cueing (for example, using simple emojis that correspond with the
Likert scale options), and the ability to request assistance in
completing the survey. Options for phone surveys and the use of
interpreters will also be included in these guidelines. Finally, the
measure developer will add a question to the survey to indicate if the
survey was
[[Page 51125]]
completed with assistance. We anticipate that the updated survey will
be available during FY 2023 so that IPFs can review it during their
implementation planning in advance of the performance period for
voluntary reporting (that is CY 2025).
Comment: Some commenters requested clarification regarding whether
facilities could add their own elements to the survey to maintain
historical trend data regarding questions that are important among
their specific patient populations. Other commenters specifically
requested the inclusion of a free-text comment section.
Response: Individual facilities can add supplemental items to the
survey instrument provided that they do not amend or remove the key
elements of the PIX survey in order to collect data for and report on
this measure. We note that IPFs may not factor supplemental items into
existing scoring procedures as this would affect reliability and
validity of this measure. Furthermore, we encourage facilities to
consider the number of supplemental questions so as not to overburden
or fatigue patients in completing the survey instrument.
Comment: One commenter recommended allowing patients to complete
surveys regularly throughout their stay.
Response: Although we believe that this may be unduly burdensome to
patients and create administrative and logistical burden for
facilities, this is not inconsistent with reporting data on the PIX
survey for this measure if the IPF only includes data for surveys
administered according to the PIX survey measure's guidelines
(specifically, PIX surveys administered beginning 24 hours prior to
discharge) in the measure results reported to CMS.
Comment: Several commenters recommended additional questions,
topics, and domains that they believe would be important to include in
a patient experience of care survey for the IPF setting. These topics
included: (1) data on racial and ethnic disparities in diagnosing,
treating, and providing care; (2) addressing patients' spiritual needs;
(3) progress towards remediating life circumstances that precipitated
the hospitalization; (4) perceptions of discharge planning and
aftercare; (5) follow-up appointment availability (were they offered
and scheduled); (6) staff cultural competency; (7) family involvement
in treatment; (8) nurses' performance; (9) quantity of food; (10)
overall rating; (11) wait time; and (12) family and caregiver
perspectives.
Response: We note that the PIX survey was developed by an
interdisciplinary team with input from patients and a patient and
family advisory council to address items that are important to patients
in this setting of care. However, as discussed previously, individual
facilities can add supplemental items to the survey to address issues
important to their patient populations or that are significant in the
historical trend data.
Comment: One commenter stated that frequency measurement (which
asks patients to recall how often something happened) versus evaluative
measurement (which asks patients to identify how well their needs were
met) can influence the magnitude of differences when evaluating patient
experience by race and ethnicity. This commenter specifically noted
that evaluative measures are typically better at identifying
disparities than frequency-based measures and recommended considering
this in developing a survey for this setting.
Response: The PIX survey uses an evaluative measurement (which asks
patients to evaluate their experience of their care) approach with a
Likert Scale (that is, strongly disagree, somewhat disagree, neutral,
somewhat agree, strongly agree, and does not apply) versus a frequency
style of evaluation (which asks patients to report whether or how
frequently something occurred).
We agree with the commenter that one strength of the evaluative
measurement approach is the ability to better identify disparities and
detect inequities and note that this was a factor in the survey design
of the PIX survey.\198\
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\198\ Linacre JM. Optimizing rating scale category
effectiveness. J Appl Meas. 2002;3(1):85-106. PMID: 11997586.
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Comment: Many commenters recommended that the survey be
administered by a peer or advocate to reduce concerns regarding
retaliation.
Response: We appreciate this recommendation and believe that peer
advocates could assist with survey administration with minimal
training. The measure developer is currently developing survey
administration guidelines which will incorporate information on the
appropriate training for staff (including peer advocates) who will be
responsible for survey administration. We anticipate that these
guidelines will be available during FY 2023 so that IPFs can review
them during their implementation planning in advance of the performance
period for voluntary reporting (that is, CY 2025).
Comment: Several commenters had questions regarding public
reporting of these data for this measure. One commenter requested
clarification regarding whether the data would be publicly reported.
Another commenter recommended that the data be accompanied by patient
demographic and clinical information to allow for stratification and
analysis.
Response: As described in section VI.H of the FY 2024 IPF PPS
proposed rule, we have an established policy for publicly displaying
the data submitted by IPFs for the IPFQR Program (88 FR 21299 through
21300). Consistent with that policy, we intend to publicly report these
data. Specifically, in accordance with section 1886(s)(4)(E) of the
Act, data that an IPF submits to CMS for the IPFQR Program will be made
publicly available on a CMS website after providing the IPF an
opportunity to review the data to be made public. In the FY 2013 IPPS/
LTCH PPS final rule (77 FR 53653 through 53654), we adopted procedures
for making data submitted under the IPFQR Program available to the
public, after an IPF has the opportunity to review such data prior to
public display, as required by section 1886(s)(4)(E) of the Act. We
adopted modifications to these procedural requirements in the FY 2014
IPPS/LTCH PPS final rule (78 FR 50897 through 50898), and the FY 2017
IPPS/LTCH PPS final rule (81 FR 57248 through 57249). Specifically,
IPFs will have a period of 30 days to review and submit corrections to
errors resulting from CMS calculations prior to the data being made
public.
We agree that the intersectionality of patient characteristics,
including the categorization of clinical populations would provide
useful information for researchers and potentially for patients and
caregivers in selecting a facility at which to receive care. However,
we note that the survey is anonymous and therefore cannot be linked to
patients' clinical data. The measure developer specifically omitted
clinical characterizations because of patients' concerns regarding
discrimination, retaliation, and uncertainty about their suspected
versus diagnosed conditions. We will consider the appropriateness and
feasibility of including demographic data with publicly reported
measure results for future public reporting.
Comment: Several commenters requested clarification on how the data
would be collected and reported. Some of these commenters stated that
IPFs with limited technological resources would find it hard to
implement this survey. Some of these commenters further stated that
without sufficient technological resources this survey
[[Page 51126]]
would be burdensome for IPFs to administer.
Response: IPFs will collect data in the facility and then report
these data to CMS using the methods described in section VI.I.4 of this
final rule, that is ``Data Submission Requirements'' under ``Procedural
Requirements.'' This aligns with previously finalized policies for
submitting data on chart-abstracted measures. We recognize that this
may be burdensome for IPFs; however, given the importance of including
a patient experience of care measure in the IPFQR Program, we believe
that the benefit of adopting this measure outweighs this burden.
Comment: One commenter requested clarification regarding whether
IPFs would be required to respond to patients to resolve issues
identified in the PIX survey prior to the patient's discharge. Another
commenter expressed concern that patients may include a threat to self
or others in their survey response which would require IPFs to review
responses to ensure that such threats were addressed prior to
discharge.
Response: We wish to clarify that the PIX survey is an anonymous
survey. Therefore, it would not be possible for IPFs to address input
from individual patients, either prior to or after discharge. We note
that there are no questions on the PIX survey, which is a series of 23
items to which patients respond using a five-point Likert scale (that
is, strongly disagree, somewhat disagree, neutral, somewhat agree,
strongly agree) or choose that the item does not apply, that address a
patient's potential threat to self or others. We acknowledge the
possibility that, during IPF staff's administration of the survey, the
patient may express to the staff member a potential threat to self or
others. However, we believe the IPF will be able to train its staff to
appropriately respond to and notify clinical and other staff of the
patient's potential threat to self or others as with any other
situation where IPF staff interact with IPF patients.
Comment: One commenter requested clarification regarding whether
completing the survey would be mandatory for patients. Another
commenter expressed concern that behavioral health patients often
refuse to complete surveys.
Response: We agree that some patients may choose not to complete a
survey. We note that, consistent with our proposal in the FY 2024 IPF
PPS proposed rule (88 FR 21301), we are requiring IPFs to develop
sampling plans that ensure that IPFs are able to submit data for 300
completed PIX surveys per year. IPFs would be required to sample from
every month throughout the entire reporting period and not stop
sampling or curtail ongoing interview activities once a certain number
of completed surveys has been attained. We recommend that in developing
sampling plans, IPFs consider the predicted rate of non-completion to
ensure that they reach 300 completed PIX surveys.
Comment: Several commenters requested clarification regarding
whether patients would be able to have assistance, such as from a
family member, friend, or peer support specialist, to complete the
survey if the patient is unable to complete the survey. One commenter
requested clarification regarding whether a parent or guardian would be
required to complete the survey for minors.
Response: The PIX survey is suitable for individuals of all ages
within the measure cohort, which includes patients who are 13 or older
at time of discharge. The survey was tested with adolescents aged 13
to17 and testing found that they were able to complete it without any
significant differences in scores compared to adults. Nonetheless, we
understand that some individuals may require assistance, and patients
must be offered the option to seek help from staff, a caregiver
(including parents or guardians), or a peer. Additionally, the measure
developer is updating the survey to include a question asking if the
patient received any assistance while completing it. We anticipate that
the updated survey will be available during FY 2023 so that IPFs can
review it during their implementation planning in advance of the
performance period for voluntary reporting (that is CY 2025)
Comment: Several commenters expressed concern that the exclusion of
patients who are unable to complete the survey due to cognitive or
intellectual limitations could lead to subjective exclusions and create
bias in the survey administration. Several of these commenters
recommended removing this exclusion, and other commenters recommended
providing standardized definitions that IPFs could apply.
Response: The measure developer is currently developing guidelines
for best practices in survey administration to enhance the
accessibility of the PIX survey and sampling integrity. All patients,
including people with intellectual and development disabilities, must
have an opportunity to participate in or benefit from the survey equal
to that afforded to others. We anticipate that these guidelines will be
available during FY 2023 so that IPFs can review them during their
implementation planning in advance of the performance period for
voluntary reporting (that is, CY 2025). We will communicate the
availability of these guidelines through regular sub-regulatory
communications.
We note that patients who are unable to complete the survey unaided
on the basis of a disability must be offered reasonable modifications,
such as the use of visual cueing (for example, using simple emojis that
correspond with the Likert scale options). We believe that inclusivity
is a key priority of adopting a patient experience of care survey and
emphasize the importance of maximizing accessibility for all patients.
Comment: Several commenters expressed concern that the data
collected by this survey may not be sufficient to improve patient
experience. Another commenter requested clarification regarding whether
the survey has been shown to improve patient outcomes. One commenter
expressed concern about the Healing Environment domain in the PIX
survey instrument because regulations and licensing requirements
heavily restrict the environment of the IPF. One commenter expressed
concern that IPFs do not have the resources to improve care based on
the results of the PIX survey.
Response: We believe that a comprehensive approach to quality must
include directly reported feedback from patients. We have consistently
stated our commitment to identifying a patient experience of care
measure for the IPF setting, and in our measure strategies, including
the Meaningful Measures 2.0 Framework, the CMS National Quality
Strategy, the Behavioral Health Strategy, and the Universal Foundation,
we have consistently identified the need for person-centered care and
engagement. Furthermore, we note that a review of 55 studies found that
within these studies it was more common to find positive associations
between patient experience and patient safety and clinical
effectiveness than no associations.\199\ However, including a measure
of patient experience demonstrates that a positive patient experience
is an important goal in its own right. This is supported by
consistently strong patient and caregiver input requesting such a
measure be adopted in the IPFQR Program and emphasizing that such a
measure is an important element of showing that we
[[Page 51127]]
believe that IPF patients should be treated with dignity and respect in
an environment in which their voices matter as part of a patient-
centered care experience. Additionally, we believe that having a
nationally standardized patient experience of care measure will allow
IPFs to compare their patient experience results with the results of
other IPFs. This will allow IPFs to identify opportunities for
improvement, including to their Healing Environment score, within the
regulatory and licensure constraints under which IPFs operate. That is,
if other similar IPFs score higher in the Healing Environment domain
despite operating within the same regulatory and licensure constraints,
this will highlight the opportunity for the IPF to improve its Healing
Environment.
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\199\ Doyle, c. Lennox, L, and Bell, D. A systematic review of
evidence on the links between patient experience and clinical safety
and effectiveness. BMJ Open. Available at: https://bmjopen.bmj.com/content/3/1/e001570.
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Comment: One commenter expressed concern that the domain names do
not appear to match the substance of the questions within the domain.
This commenter expressed concern that there may be overlap or
inconsistencies between the use of ``treatment team'' and ``nursing
team.''
Response: We appreciate this concern; however, we believe the
domain labels have been appropriately applied. Specifically, the four-
domain survey aligned with the theoretical basis of patient experience
and was chosen through extensive focus group testing. Further,
decisions around domains and their labels were based on the degree to
which individual items statistically coalesced around central themes.
We noted that patients in focus groups rarely distinguished roles among
their care teams. Functionally, medical providers and social workers
operate in a collaborative framework to guide treatment and coordinate
aftercare. Thus, questions about patients' relationships with their
treatment team center around their interactions with those who provide
medical and therapeutic care. The Nursing Presence domain was
identified as a separate domain due to the distinctive nature of
nurses' roles in comprehensively caring for all patients on the unit in
support of the treatment team. We agree with the measure developer that
this important distinction merited a separate domain to represent the
unique work of the varying team members with whom patients interact.
Comment: Some commenters expressed concerns that this measure has
not been endorsed by the CBE.
Response: We note that following additional testing, the measure
developer intends to submit this measure to the CBE for endorsement.
While we recognize the value of measures undergoing CBE endorsement
review, given the urgency of adopting a patient experience of care
measure for this setting, as there are currently no CBE-endorsed
measures that address IPF patient experience of care, we believe it is
important to implement this measure beginning with voluntary reporting
of CY 2025 data followed by mandatory reporting beginning with CY 2026
data, reported to CMS in CY 2027 and affecting the FY 2028 payment
determination. We note that under section 1886(s)(4)(D)(ii) of the Act
the Secretary may specify a measure that is not so endorsed as long as
due consideration is given to measures that have been endorsed or
adopted by a consensus organization identified by the Secretary. We
reviewed measures endorsed by consensus organizations and were unable
to identify any other measures on this topic endorsed by a consensus
organization, and therefore, we believe the exception in section
1886(s)(4)(D)(ii) of the Act applies.
Comment: One commenter requested clarification on who developed the
survey, whether it is proprietary, and if so, how IPFs will obtain
licenses to use the survey.
Response: As described in the FY 2024 IPF PPS proposed rule (88 FR
21288), the PIX survey was developed by a team at the Yale University,
Yale New Haven Psychiatric Hospital and is in the public domain. We
note that the measure developer is currently developing guidelines for
best practices in survey administration, and we strongly encourage
staff who will be responsible for administering the survey to review
these guidelines as soon as they become available. Because the measure
developer has made the PIX survey available in the public domain, there
is no certification or license required to administer the PIX survey.
Comment: One commenter expressed concern that there are too many
questions for patients to complete.
Response: We understand the importance of balancing the number of
survey questions to improve completion rates with minimal burden to the
patient, while including a sufficient range of questions to address the
most important aspects of patients' experiences about the care they
received. We note that the PIX survey has 23 items, which is comparable
to the number of questions in other patient experience of care survey
instruments. Specifically, two other surveys which address inpatient
care include the HCAHPS survey, which has 29 questions, and the
Inpatient Consumer Survey (ICS), which has 28 items.
Comment: One commenter opposed adopting this survey in a pay-for-
performance program.
Response: We note that the IPFQR Program is a pay-for-reporting
program (that is, IPFs that comply with all requirements and submit
required data under the IPFQR Program receive their full payment
update) and that there are not currently any Medicare pay-for-
performance programs (that is, programs which adjust payment based on
the performance on measures) which address the IPF setting.
Comment: Some commenters requested clarification regarding whether
the measure would be scored with ``top-box'' scoring or with mean
scores, because the MUC List and the proposed rule described different
methods.
Response: We considered ``top-box'' scoring and mean scores as we
identified an approach to adopting and publicly reporting the PIX
survey measure in the IPFQR Program. Specifically, we considered
modeling the ``top-box'' scoring used for reporting performance on the
HCAHPS measure in which data are reported based on the percent of
respondents who selected the most positive response (that is, the
``top-box''). However, we believe that mean scores (that is, the
numerical average calculated by assigning each response a numerical
value from 1--the least positive, to 5 the most positive, summing the
scores, and dividing that value by the number of responses) provide
information that is more meaningful to patients and their caregivers
who are more likely to be familiar with mean scores as opposed to
``top-box'' scores. Therefore, we decided to propose mean scores, which
we described in the FY 2024 IPF PPS proposed rule (88 FR 21289). We
note that the MUC list submission acknowledged the possibility that
mean scores would be useful for reporting with the statement that ``it
may be useful for the distribution of total Likert-scale responses to
be made available during initial implementation.''
Comment: One commenter expressed support for reporting separate
rates for each domain in addition to the overall rate. This commenter
stated that this level of data will improve patient choice and support
IPFs' quality improvement efforts.
Response: We thank this commenter for the support and agree that
the increased level of detail will improve patient choice and support
IPF's quality improvement efforts.
Comment: Several commenters requested clarification regarding
[[Page 51128]]
whether there will be a one-year or two-year voluntary reporting
period.
Response: We wish to clarify that, consistent with our proposal in
the FY 2024 IPF PPS proposed rule (88 FR 21290), there will be a 1-year
voluntary reporting period. IPFs that wish to participate in the
voluntary reporting period will be able to report CY 2025 data to CMS
in CY 2026. Beginning with CY 2026 data, which will be reported to CMS
in CY 2027, all IPFs will be required to report these data to CMS and
failure to do so would affect their payment determination for FY 2028.
Comment: Several commenters expressed support for adoption of this
measure for voluntary reporting of CY 2025 data in CY 2026 followed by
mandatory reporting beginning with CY 2026 data affecting the FY 2028
payment determination to ensure there is a patient experience measure
in the IPFQR Program as soon as technically feasible.
Response: We thank these commenters for their support.
Final Decision: After consideration of the public comments we
received, we are finalizing adoption of the PIX survey measure as
proposed.
E. Modification of the COVID-19 Vaccination Coverage Among Healthcare
Personnel (HCP) Measure Beginning With the Quarter 4 CY 2023 Reporting
Period/FY 2025 Payment Determination
1. Background
On January 31, 2020, the Secretary of the Department of Health and
Human Services declared a public health emergency (PHE) for the United
States in response to the global outbreak of SARS-COV-2, a novel (new)
coronavirus that causes a disease named ``coronavirus disease 2019''
(COVID-19).\200\ Subsequently, multiple quality reporting programs
including the Hospital IQR Program (86 FR 45374) and the IPFQR Program
(86 FR 42633 through 42640) adopted the COVID-19 Vaccination Coverage
Among Healthcare Personnel (HCP) measure. The COVID-19 Vaccination
Coverage Among Healthcare Personnel (HCP) measure adopted in the IPFQR
Program in the FY 2022 IPF PPS final rule (86 FR 42633 through 42650)
requires each IPF to calculate the percentage of HCP eligible to work
in the IPF for at least one day during the reporting period, excluding
persons with contraindications to the COVID-19 vaccine, who have
received a complete vaccination course against SARS-CoV-2 (86 FR 42633
through 42640).
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\200\ U.S. Dept of Health and Human Services, Office of the
Assistant Secretary for Preparedness and Response. (2020).
Determination that a Public Health Emergency Exists. Available at:
https://www.phe.gov/emergency/news/healthactions/phe/Pages/2019-nCoV.aspx.
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COVID-19 has continued to spread domestically and around the world
with more than 103.9 million cases and 1.13 million deaths in the
United States as of June 19,2023.\201\ In recognition of the ongoing
significance and complexity of COVID-19, the Secretary renewed the PHE
on April 21, 2020, July 23, 2020, October 2, 2020, January 7, 2021,
April 15, 2021, July 19, 2021, October 15, 2021, January 14, 2022,
April 12, 2022, July 15, 2022, October 13, 2022, January 11, 2023, and
February 9, 2023.\202\ While the PHE status ended on May 11, 2023,\203\
HHS has stated that the public health response to COVID-19 remains a
public health priority with a whole of government approach to
combatting the virus, including through vaccination efforts.\204\
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\201\ Centers for Disease Control and Prevention. COVID Data
Tracker. Accessed February 13, 2023. Available at: https://covid.cdc.gov/covid-data-tracker/#datatracker-home.
\202\ U.S. Dept. of Health and Human Services. Office of the
Assistant Secretary for Preparedness and Response. (2023). Renewal
of Determination that a Public Health Emergency Exists. Available
at: https://aspr.hhs.gov/legal/PHE/Pages/covid19-11Jan23.aspx.
\203\ https://www.whitehouse.gov/wp-content/uploads/2023/01/SAP-H.R.-382-H.J.-Res.-7.pdf.
\204\ U.S. Dept. of Health and Human Services. Fact Sheet:
COVID-19 Public Health Emergency Transition Roadmap. February 9,
2023. Available at: https://www.hhs.gov/about/news/2023/02/09/fact-sheet-covid-19-public-health-emergency-transition-roadmap.html.
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In the FY 2022 IPF PPS final rule (86 FR 42633 through 42635) and
in our Revised Guidance for Staff Vaccination Requirements,\205\ we
stated that vaccination is a critical part of the nation's strategy to
effectively counter the spread of COVID-19. We continue to believe it
is important to incentivize and track HCP vaccination through quality
measurement across care settings, including IPFs, in order to protect
HCP, patients, and caregivers, and to help sustain the ability of HCP
to continue serving their communities throughout the PHE and beyond.
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\205\ Centers for Medicare & Medicaid Services. Revised Guidance
for Staff Vaccination Requirements QSO-23-02-ALL. October 26, 2022.
Available at: https://www.cms.gov/files/document/qs0-23-02-all.pdf.
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At the time we issued the FY 2022 IPF PPS final rule where we
adopted the COVID-19 Vaccination Coverage Among Healthcare Personnel
(HCP) measure, the Food and Drug Administration (FDA) had issued
emergency use authorizations (EUAs) for initial and primary adult
vaccines manufactured by Pfizer-BioNTech,\206\ Moderna,\207\ and
Janssen.\208\ On August 23, 2021, the FDA issued an approval for the
Pfizer-BioNTech vaccine, now marketed as Comirnaty.\209\ The FDA issued
approval for the Moderna vaccine, marketed as Spikevax, on January 31,
2022 \210\ and an EUA for the Novavax adjuvanted vaccine on July 13,
2022.\211\ The FDA also issued EUAs for COVID-19 single vaccine booster
doses in September 2021 \212\ and October 2021 \213\ for certain
populations and in November 2021 \214\ for all individuals 18 years of
age and older. EUAs were subsequently issued for a second vaccine
booster dose in March 2022 \215\
[[Page 51129]]
and for bivalent or ``updated'' booster doses in August 2022.\216\
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\206\ Food and Drug Administration. (December 2020). FDA Takes
Key Action in Fight Against COVID-19 By Issuing Emergency Use
Authorization for First COVID-19 Vaccine. Available at: https://www.fda.gov/news-events/press-announcements/fda-takes-key-action-fight-against-covid-19-issuing-emergency-use-authorization-first-covid-19.
\207\ Food and Drug Administration. (December 2020). FDA Takes
Additional Action in Fight Against COVID-19 By Issuing Emergency Use
Authorization for Second COVID-19 Vaccine. Available at: https://www.fda.gov/news-events/press-announcements/fda-takes-additional-action-fight-against-covid-19-issuing-emergency-use-authorization-second-covid.
\208\ Food and Drug Administration. (February 2021). FDA Issues
Emergency Use Authorization for Third COVID-19 Vaccine. Available
at: https://www.fda.gov/news-events/press-announcements/fda-issues-emergency-use-authorization-third-covid-19-vaccine.
\209\ Food and Drug Administration. (August 2021). FDA Approves
First COVID-19 Vaccine. Available at: https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine.
\210\ Food and Drug Administration. (January 2022). Coronavirus
(COVID-19) Update: FDA Takes Key Action by Approving Second COVID-19
Vaccine. Available at: https:/www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-takes-key-action-approving-second-covid-19-vaccine.
\211\ Food and Drug Administration. (July 2022). Coronavirus
(COVID-19) Update: FDA Authorizes Emergency Use of Novavax COVID-19
Vaccine, Adjuvanted. Available at: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-emergency-use-novavax-covid-19-vaccine-adjuvanted.
\212\ Food and Drug Administration. (September 2021). FDA
Authorizes Booster Dose of Pfizer-BioNTech COVID-19 Vaccine for
Certain Populations. Available at: https://www.fda.gov/news-events/press-announcements/fda-authorizes-booster-dose-pfizer-biontech-covid-19-vaccine-certain-populations.
\213\ Food and Drug Administration. (October 2021). Coronavirus
(COVID-19) Update: FDA Takes Additional Actions on the Use of a
Booster Dose for COVID-19 Vaccines. Available at: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-takes-additional-actions-use-booster-dose-covid-19-vaccines.
\214\ Food and Drug Administration. (November 2021). Coronavirus
(COVID-19) Update: FDA Expands Eligibility for COVID-19 Vaccine
Boosters. Available at: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-expands-eligibility-covid-19-vaccine-boosters.
\215\ Food and Drug Administration. (March 2022). Coronavirus
(COVID-19) Update: FDA Authorizes Second Booster Dose of Two COVID-
19 Vaccines for Older and Immunocompromised Individuals. Available
at: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-second-booster-dose-two-covid-19-vaccines-older-and.
\216\ Food and Drug Administration. (August 2022). Coronavirus
(COVID-19) Update: FDA Authorizes Moderna, Pfizer-BioNTech Bivalent
COVID-19 Vaccines for Use as a Booster Dose. Available at: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-moderna-pfizer-biontech-bivalent-covid-19-vaccines-use.
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In the FY 2022 IPF PPS final rule, we stated that data
demonstrating the effectiveness of COVID-19 vaccines to prevent
asymptomatic infection or transmission of SARS-COV-2, the novel (new)
coronavirus that causes COVID-19, were limited (86 FR 42634). While the
impact of COVID-19 vaccines on asymptomatic infection and transmission
was not yet fully known at the time of the FY 2022 IPF PPS final rule,
there were robust data available on COVID-19 vaccine effectiveness
across multiple populations against symptomatic infection,
hospitalization, and death. Two-dose COVID-19 vaccines from Pfizer-
BioNTech and Moderna had been found to be 88 percent and 93 percent
effective against hospitalization for COVID-19, respectively, over 6
months for adults over age 18 without immunocompromising
conditions.\217\ During a SARS-COV-2 surge in the spring and summer of
2021, 92 percent of COVID-19 hospitalizations and 91 percent of COVID-
19-associated deaths were reported among persons not fully
vaccinated.\218\ Real-world studies of population-level vaccine
effectiveness indicated similarly high rates of effectiveness in
preventing SARS-COV-2 infection among frontline workers in multiple
industries, with a 90 percent effectiveness in preventing symptomatic
and asymptomatic infection from December 2020 through August 2021.\219\
Vaccines have also been highly effective in real-world conditions (that
is, vaccines have continued to be highly effective in conditions other
than clinical trials) at preventing COVID-19 in HCP with up to 96
percent effectiveness for fully vaccinated HCP, including those at risk
for severe infection and those in racial and ethnic groups
disproportionately affected by COVID-19.\220\ In the presence of high
community prevalence of COVID-19, residents of nursing homes with low
staff vaccination coverage had cases of COVID-19-related deaths 195
percent higher than those among residents of nursing homes with high
staff vaccination coverage.\221\ Currently available data demonstrate
that COVID-19 vaccines are effective and prevent severe disease,
including hospitalization, and death.
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\217\ Centers for Disease Control and Prevention. (September 24,
2021). Morbidity and Mortality Weekly Report (MMWR). Comparative
Effectiveness of Moderna, Pfizer-BioNTech, and Janssen (Johnson &
Johnson) Vaccines in Preventing COVID-19 Hospitalizations Among
Adults Without Immunocompromising Conditions--United States, March-
August 2021. Available at: https://cdc.gov/mmwr/volumes/70/wr/mm7038e1.htm?s_cid=mm7038e1_w.
\218\ Centers for Disease Control and Prevention. (September 10,
2021). Morbidity and Mortality Weekly Report (MMWR). Monitoring
Incidence of COVID-19 Cases, Hospitalizations, and Deaths, by
Vaccination Status--13 U.S. Jurisdictions, April 4-July 17, 2021.
Available at: https://cdc.gov.mmwr/volumes/70/wr/mm7037e1.htm.
\219\ Centers for Disease Control and Prevention. (August 27,
2021). Morbidity and Mortality Weekly Report (MMWR). Effectiveness
of COVID-19 Vaccines in Preventing SARS-COV-2 Infection Among
Frontline Workers Before and During B.1.617.2 (Delta) Variant
Predominance--Eight U.S. Locations, December 2020-August 2021.
Available at: https://cdc.gov/mmwr/volume/70/wr/mm7034e4.htm
\220\ Pilishivi, T. et al. (December 2022). Effectiveness of
mRNA Covid-19 Vaccine among U.S. Health Care Personnel. New England
Journal of Medicine. 2021 Dec 16;385(25):e90. Available online at:
https://pubmed.ncbi.nlm.nih.gov/34551224/.
\221\ McGarry BE et al. (January 2022). Nursing Home Staff
Vaccination and Covid-19 Outcomes. New England Journal of Medicine.
2022 Jan 27;386(4):397-398. Available online at: https://pubmed.ncbi.nlm.nih.gov/34879189/.
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As SARS-COV-2 persists and evolves, our COVID-19 vaccination
strategy must remain responsive. When we adopted the COVID-19
Vaccination Coverage Among HCP measure in the FY 2022 IPF PPS final
rule, we stated that the need for booster doses of the COVID-19 vaccine
had not been established and no additional doses had been recommended
(86 FR 42639). We also stated that we believed the numerator was
sufficiently broad to include potential future boosters as part of a
``complete vaccination course'' and that the measure was sufficiently
specified to address boosters (86 FR 42639). Since we adopted the
COVID-19 Vaccination Coverage Among HCP measure in the FY 2022 IPF PPS
final rule, new variants of SARS-COV-2 have emerged around the world
and within the United States. Specifically, the Omicron variant (and
its related subvariants) is listed as a variant of concern by the
Centers for Disease Control and Prevention (CDC) because it spreads
more easily than earlier variants.\222\ Vaccine manufacturers have
responded to the Omicron variant by developing bivalent COVID-19
vaccines, which include a component of the original virus strain to
provide broad protection against COVID-19 and a component of the
Omicron variant to provide better protection against COVID-19 caused by
the Omicron variant.\223\ These booster doses of the bivalent COVID-19
vaccine have been shown to increase immune response to SARS-COV-2
variants, including Omicron, particularly in individuals who are more
than 6 months removed from receipt of their primary series.\224\ The
FDA issued EUAs for two bivalent COVID-19 vaccine booster doses, one
from Pfizer-BioNTech \225\ and one from Moderna,\226\ and strongly
encourages anyone who is eligible to consider receiving a booster dose
with a bivalent COVID-19 vaccine to provide better protection against
currently circulating variants.\227\ COVID-19 booster doses are
associated with a greater reduction in infections among HCP and their
patients relative to those who only received primary series
vaccination. One study showed a rate of breakthrough infections among
HCP who received only the two-dose regimen of the COVID-19 vaccine of
21.4 percent compared to a rate of 0.7 percent among HCP who received a
third dose of the COVID-19 vaccine.\228\
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\222\ Centers for Disease Control and Prevention. (August 2021).
Variants of the Virus. Available at: https://www.cdc.gov/coronavirus/2019-ncov/variants/.
\223\ Food and Drug Administration. (November 2022). COVID-19
Bivalent Vaccine Boosters.
\224\ Chalkias, S et al. (October 2022). A Bivalent Omicron-
Containing Booster Vaccine against Covid-19. N Engl J Med 2022;
387:1279-1291. Available online at: https://www.nejm.org/doi/full/10.1056/NEJMoa2208343.
\225\ Food and Drug Administration. (November 2022). Pfizer-
BioNTech COVID-19 Vaccines. Available at: https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccines.
\226\ Food and Drug Administration. (November 2022). Moderna
COVID-19 Vaccines. Available at: https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/moderna-covid-19-vaccines.
\227\ Food and Drug Administration. (August 2022). Coronavirus
(COVID-19) Update: FDA Authorizes Moderna, Pfizer-BioNTech Bivalent
COVID-19 Vaccines for Use as a Booster Dose. Available at: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-moderna-pfizer-biontech-bivalent-covid-19-vaccines-use.
\228\ Oster Y et al. (May 2022). The effect of a third BNT162b2
vaccine on breakthrough infections in health care workers: a cohort
analysis. Clin Microbiol Infect. 2022 May;28(5): 735.e1-735.e3.
Available online at: https://pubmed.ncbi.nlm.nih.gov/35143997/.
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Despite the efficacy of COVID-19 vaccination generally, data
submitted to the CDC via the National Healthcare Safety Network (NHSN)
demonstrate clinically significant variation in booster dose
vaccination rates across facilities, including IPFs. During the first
quarter of 2022, IPFs reported a median
[[Page 51130]]
coverage rate of booster or additional dose(s) of 19.1 percent, with an
interquartile range of 8.7 percent to 37.9 percent. These data, which
show a performance gap in booster coverage, indicate that there is
opportunity to improve booster vaccination coverage among HCP in
IPFs.\229\
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\229\ Measure Applications Partnership (MAP) Hospital Workgroup
Preliminary Analyses. Available at: https://mmshub.cms.gov/sites/default/files/map-hospital-measure-specifications-manual-2022.pdf.
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We believe that vaccination remains the most effective means to
prevent the worst consequences of COVID-19, including severe illness,
hospitalization, and death. Given the availability of vaccine efficacy
data, EUAs issued by the FDA for bivalent boosters, the continued
presence of SARS-COV-2 in the United States, and variance among rates
of booster dose vaccination, it is important to modify the COVID-19
Vaccination Coverage Among HCP measure to refer explicitly to HCP who
receive primary series and booster vaccine doses in a timely manner.
Given the persistent spread of COVID-19, we continue to believe that
monitoring and surveillance of vaccination rates among HCP is important
and provides patients, beneficiaries, and their caregivers with
information to support informed decision-making.
Beginning with the fourth quarter of the CY 2023 reporting period/
FY 2025 payment determination, we proposed to modify the COVID-19
Vaccination Coverage Among HCP measure in the IPFQR Program to replace
the term ``complete vaccination course'' with the term ``up-to-date''
in the HCP vaccination definition. We also proposed to update the
numerator to specify the time frames within which an HCP is considered
``up-to-date'' with recommended COVID-19 vaccines, including booster
doses.
In the FY 2022 IPF PPS final rule (86 FR 42638), we stated, and
reiterate now, that the COVID-19 Vaccination Coverage Among HCP measure
is a process measure that assesses HCP vaccination coverage rates.
Unlike outcome measures, process measures do not assess a particular
clinical outcome.
2. Overview of Measure
The proposed COVID-19 Vaccination Coverage Among HCP measure is a
process measure developed by the CDC to track COVID-19 vaccination
coverage among HCP in settings such as acute care facilities, including
IPFs, and post-acute care facilities.
We refer readers to the FY 2022 IPF PPS final rule (86 FR 42635
through 42636) for more information on the initial review of the
current COVID-19 Vaccination Coverage Among HCP measure by the Measure
Applications Partnership (MAP). We included an updated version of the
proposed modification of the COVID-19 Vaccination Coverage Among HCP
measure on the list of measures under consideration (MUC List), which
is published annually on behalf of CMS by the CBE with which the
Secretary must contract as required by section 1890(a) of the Act, for
the 2022 to 2023 pre-rulemaking cycle for consideration by the MAP.
In December 2022, the MAP Hospital Workgroup discussed the proposed
modification of the COVID-19 Vaccination Coverage Among HCP measure.
The MAP Hospital Workgroup stated that the proposed modification of the
current measure captures ``up-to-date'' vaccination information in
accordance with the CDC's recommendations, which have been updated
since their initial development. Additionally, the MAP Hospital
Workgroup appreciated that the modified measure's denominator is
broader and simplified from seven categories of healthcare personnel to
four.\230\
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\230\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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During review on December 6 and 7, 2022, the MAP Health Equity
Advisory Group highlighted the importance of COVID-19 measures and
asked whether the proposed modified measure excludes individuals with
contraindications to Food and Drug Administration (FDA) authorized or
approved COVID-19 vaccines, and whether the measure will be stratified
by demographic factors.\231\ The CDC, the measure developer for this
measure, responded to the question regarding individuals with
contraindications by confirming that HCP with contraindications to the
vaccines are excluded from the measure denominator. The CDC further
explained that the modified measure will not be stratified since the
data are submitted at an aggregate rather than an individual level.
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\231\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
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During review on December 8 through 9, 2022, the MAP Rural Health
Advisory Group expressed concerns about data collection burden, citing
that collection is performed manually and that small rural hospitals
may not have employee health software.\232\ The measure developer (that
is, the CDC) acknowledged the challenge of getting adequate
documentation and emphasized the goal to ensure the measure does not
present a burden on providers. The measure developer also noted that
the model used for this measure is based on the Influenza Vaccination
Coverage Among HCP measure (CBE #0431), and it intends to utilize a
similar approach to the modified COVID-19 Vaccination Coverage Among
HCP measure if vaccination strategy becomes seasonal. The modified
COVID-19 Vaccination Coverage Among HCP measure received conditional
support for rulemaking pending testing indicating the measure is
reliable and valid, and endorsement by the CBE. The MAP noted that the
previous version of the measure received endorsement from the CBE (CBE
#3636) \233\ and that the CDC intends to submit the proposed updated
measure for endorsement.
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\232\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
\233\ Centers for Medicare & Medicaid Services. 2022-2023 MAP
Final Recommendations. Available at: https://mmshub.cms.gov/measure-lifecycle/measure-implementation/pre-rulemaking/lists-and-reports.
and CMS Measures Inventory Tool. Available at: https://cmit.cms.gov/cmit/#/MeasureView?variantId=5273§ionNumber=1.
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a. Measure Specifications
The modification of the COVID-19 Vaccination Coverage Among HCP
measure will require that IPFs continue to collect data at least one
week each month for each of the three months in a quarter.
The denominator is the number of HCP eligible to work in the
facility for at least one day during the reporting period, excluding
persons with contraindications to COVID-19 vaccination that are
described by the CDC.\234\ There are not any changes to the denominator
exclusions for the current COVID-19 Vaccination Coverage Among HCP
measure, and the modified COVID-19 Vaccination Coverage Among HCP
measure will continue to exclude otherwise denominator-eligible HCPs
with contraindications as defined by the CDC.\235\ IPFs report the
following four
[[Page 51131]]
categories of HCP to NHSN \236\; the first three categories are
included in the measure denominator:
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\234\ Centers for Disease Control and Prevention. (2022).
Contraindications and precautions. Available at: https://www.cdc.gov/vaccines/covid-19/clinical-considerations/interim-considerations-us.html#contraindications.
\235\ Centers for Disease Control and Prevention. (2022).
Contraindications and precautions. Available at: https://www.cdc.gov/vaccines/covid-19/clinical-considerations/interim-considerations-us.html#contraindications.
\236\ https://www.cdc.gov/nhsn/pdfs/nqf/covid-vax-hcpcoverage-rev-2023-508.pdf.
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1. Employees: This category includes all persons who receive a
direct paycheck from the IPF (that is, on the IPF's payroll),
regardless of clinical responsibility or patient contact.
2. Licensed independent practitioners (LIPs): This category
includes physicians (MD, DO), advanced practice nurses, and physician
assistants who are affiliated with the IPF but are not directly
employed by it (that is, they do not receive a paycheck from the IPF),
regardless of clinical responsibility or patient contact. Post-
residency fellows are also included in this category if they are not on
the IPF's payroll.
3. Adult students/trainees and volunteers: This category includes
medical, nursing, or other health professional students, interns,
medical residents, or volunteers aged 18 or older who are affiliated
with the healthcare facility, but are not directly employed by it (that
is, they do not receive a paycheck from the facility), regardless of
clinical responsibility or patient contact.
4. Other contract personnel: Contract personnel are defined as
persons providing care, treatment, or services at the IPF through a
contract who do not fall into any of the previously discussed
denominator categories. Please note that this also includes vendors
providing care, treatment, or services at the facility who may or may
not be paid through a contract. Facilities are required to enter data
on other contract personnel for submission in the NHSN application, but
reporting for this category is not included in the COVID-19 Vaccination
Coverage Among HCP measure.
The numerator is the cumulative number of HCP in the denominator
population who are ``up-to-date'' with CDC recommended COVID-19
vaccines. IPFs would refer to the CDC's guidance, to determine the
then-applicable definition of ``up-to-date,'' as of the first day of
the applicable reporting quarter. The CDC's guidance can be found at:
https://www.cdc.gov/nhsn/pdfs/hps/covidvax/UpToDateGuidance-508.pdf.
For purposes of NHSN surveillance, the CDC used the following
definition of ``up-to-date'' during the fourth quarter of CY 2022
surveillance period (September 26, 2022 through December 25, 2022):
1. Individuals who received an updated bivalent \237\ booster dose,
or
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\237\ The updated (bivalent) Moderna and Pfizer-BioNTech
boosters target the most recent Omicron subvariants. The updated
(bivalent) boosters were recommended by the CDC on 9/2/2022. As of
this date, the original, monovalent mRNA vaccines are no longer
authorized as a booster dose for people ages 12 years and older.
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2a. Individuals who received their last booster dose less than 2
months ago, or
2b. Individuals who completed their primary series \238\ less than
2 months ago.
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\238\ Completing a primary series means receiving a two-dose
series of a COVID-19 vaccine or a single dose of Janssen/J&J COVID-
19 vaccine.
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Subsequent to the publication of the FY 2024 IPF PPS proposed rule,
the CDC has updated the definition of ``up-to-date'' for the second
quarter of CY 2023 surveillance period:
1. Individuals who received an updated bivalent \239\ booster dose,
or
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\239\ The updated (bivalent) Moderna and Pfizer-BioNTech
boosters target the most recent Omicron subvariants. The updated
(bivalent) boosters were recommended by the CDC on 9/2/2022. As of
this date, the original, monovalent mRNA vaccines are no longer
authorized as a booster dose for people ages 12 years and older.
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2. Individuals who completed their primary series \240\ less than 2
months ago.
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\240\ Completing a primary series means receiving a two-dose
series of a COVID-19 vaccine or a single dose of Janssen/J&J COVID-
19 vaccine.
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We refer readers to https://www.cdc.gov/nhsn/nqf/ for
more details on the modified measure specifications.
We proposed that public reporting of the modified version of the
COVID-19 Vaccination Coverage Among HCP measure would begin with the
October 2024 Care Compare refresh, or as soon as technically feasible
after that refresh.
b. CBE Endorsement
The current version of the COVID-19 Vaccination Coverage Among HCP
measure received CBE endorsement (CBE #3636, ``Quarterly Reporting of
COVID-19 Vaccination Coverage Among Healthcare Personnel'') on July 26,
2022.\241\
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\241\ CMS Measures Inventor Tool. COVID-19 Vaccination Coverage
among Healthcare Personnel. Available at: https://cmit.cms.gov/cmit/#/MeasureView?variantId=5273§ionNumber=1.
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Although section 1886(s)(4)(D)(i) of the Act generally requires
that measures specified by the Secretary must be endorsed by the entity
with a contract under section 1890(a) of the Act, section
1886(s)(4)(D)(ii) of the Act states that in the case of a specified
area or medical topic determined appropriate by the Secretary for which
a feasible and practical measure has not been endorsed by the entity
with a contract under section 1890(a) of the Act, the Secretary may
specify a measure that is not so endorsed as long as due consideration
is given to a measure that has been endorsed or adopted by a consensus
organization identified by the Secretary.
We reviewed measures endorsed by consensus organizations and were
unable to identify any other measures on this topic endorsed by a
consensus organization; therefore, we believe the exception in section
1886(s)(4)(D)(ii) of the Act applies. The CDC, as the measure
developer, is currently pursuing endorsement for the modified version
of the measure as the current version of the measure has already
received endorsement.
3. Data Collection, Submission, and Reporting
We refer readers to the FY 2022 IPF PPS final rule (86 FR 42636
through 42640) for information on data submission and reporting of the
current COVID-19 Vaccination Coverage Among HCP measure. While we did
not propose any changes to the data submission or reporting process, we
proposed that reporting of the updated modified measure would begin
with the fourth quarter of CY 2023 reporting period for FY 2025 payment
determination. Beginning with the FY 2026 payment determination, we
proposed that IPFs would be required to submit data for the modified
measure for the entire calendar year.
Under the data submission and reporting process, IPFs collect the
numerator and denominator for the COVID-19 Vaccination Coverage Among
HCP measure for at least one self-selected week during each month of
the reporting quarter and submit the data to the CDC's National Health
Safety Network (NHSN) Healthcare Personnel Safety (HPS) Component
before the quarterly deadline. If an IPF submits more than one week of
data in a month, the CDC would use most recent week's data to calculate
the measure results which would be publicly reported. Each quarter, the
CDC calculates a single quarterly COVID-19 HCP vaccination coverage
rate for each IPF, which is calculated by taking the average of the
data from the three weekly rates submitted by the IPF for that quarter.
CMS publicly reports each quarterly COVID-19 HCP vaccination coverage
rate as calculated by the CDC based on the data IPFs submit to the NHSN
(86 FR 42636 through 42640).
We invited public comment on our proposal.
Comment: Some commenters supported the proposed modification to the
COVID-19 Vaccination Coverage Among HCP measure. One of these
commenters stated that the modified specifications would lead to
increased vaccination and booster adoption among
[[Page 51132]]
HCP. One commenter stated that patients with mental illness are more
vulnerable to COVID-19 driving the increased need for their providers
to be vaccinated.
Response: We thank the commenters for their support. We agree that
vaccination plays a critical part of the nation's strategy to
effectively counter the spread of COVID-19. We continue to believe it
is important to incentivize and track rates of vaccination among HCP
through quality measurement across care settings, including the IPF
setting, in order to protect healthcare workers, patients, and
caregivers, and to help sustain the ability of HCP in each of these
care settings to continue serving their communities.
Comment: Several commenters did not support updating the
specifications for the COVID-19 Vaccination Coverage Among HCP measure
because the PHE has expired and the Conditions of Participation (COPs)
for hospitals have been revised to no longer require reporting of these
data. Some of these commenters requested clarification regarding
whether the change in COPs means that we will remove the measure from
our quality reporting programs. One commenter expressed concern that
retaining measurement of COVID-19 Vaccination Coverage Among HCP after
the vaccination requirement has been removed from COPs sends an
inconsistent message regarding CMS's priorities.
Response: As commenters noted, the PHE for COVID-19 expired on May
11, 2023.\242\ Since May 11, 2023, some state and federal reporting
requirements have changed. While CMS requirements for Medicare and
Medicaid-certified providers and suppliers to ensure that their staff
were fully vaccinated for COVID-19 have ended with the expiration of
the COVID-19 PHE (88 FR 36488), CMS revised the hospital and critical
access hospitals (CAHs) infection prevention and control Condition of
Participation so that hospitals and CAHs will continue to report on a
reduced number of COVID-19 data elements after the conclusion of the
COVID- 19 PHE until April 30, 2024, unless the Secretary establishes an
earlier end date.\243\ While these changes may impact certain aspects
of facility reporting on COVID-19 data, we note that the reporting
requirements of the IPFQR Program are distinct from those related to
the expiration of the COVID-19 PHE and facilities participating in the
IPFQR Program are required to report the COVID-19 Vaccination Coverage
Among HCP measure. We further note that in our final rule removing
staff vaccination requirements, we clarified that we were aligning our
approach with that for other infectious diseases, specifically
influenza, and that we would encourage ongoing COVID-19 vaccination
through our quality reporting and value-based incentive programs (88 FR
38486).
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\242\ U.S. Dept. of Health and Human Services. Fact Sheet:
COVID-19 Public Health Emergency Transition Roadmap. February 9,
2023. Available at: https://www.hhs.gov/about/news/2023/02/09/fact-sheet-covid-19-public-health-emergency-transition-roadmap.html.
\243\ https://www.hhs.gov/about/news/2023/05/09/fact-sheet-end-of-the-covid-19-public-health-emergency.html.
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We believe this measure continues to align with our goals to
promote wellness and disease prevention. Under CMS' Meaningful Measures
Framework 2.0, the COVID-19 Vaccination Coverage Among HCP measure
addresses the quality priorities of ``Immunizations'' and ``Public
Health'' through the Meaningful Measures Area of ``Wellness and
Prevention.'' Under the National Quality Strategy, the measure
addresses the goal of ``Safety'' under the priority area ``Safety and
Resiliency.'' Our response to COVID-19 is not fully dependent on the
emergency declaration for the COVID-19 PHE and, beyond the end of the
COVID-19 PHE, we continue to work to protect individuals and
communities from the virus and its worst impacts by supporting access
to COVID-19 vaccines, treatments, and tests.
Comment: Many commenters did not support updating the COVID-19
Vaccination Coverage Among HCP measure because of concerns that the
frequency of changes to the CDC's definition of ``up-to-date'' combined
with the uncertainty around future vaccination schedules creates
unnecessary burden for facilities. Some of these commenters recommended
allowing voluntary reporting until the appropriate definitions and
guidance are stable. One commenter stated that understanding how
changing guidelines apply to all members of staff (such as those with
risk factors) is burdensome. Others stated that publicly reporting
these data may not be meaningful to consumers due to the changing
definitions and the time lag between collection and public reporting.
Response: Since the adoption of the current version of the measure,
the public health response to COVID-19 has necessarily adapted to
respond to the changing nature of the virus's transmission and
community spread. When we finalized the adoption of the COVID-19
Vaccination Coverage Among HCP measure in the FY 2022 IPF PPS final
rule (86 FR 42640), we received several comments encouraging us to
continue to update the measure as new evidence on COVID-19 continues to
arise and we stated our intention to continue to work with partners
including FDA and CDC to consider any updates to the measure in future
rulemaking as appropriate. We believe that the measure modification
aligns with the CDC's responsive approach to COVID-19 and will continue
to support vaccination as the most effective means to prevent the worst
consequences of COVID-19, including severe illness, hospitalization,
and death. We agree with commenters who observe that there is a delay
between data collection and public reporting for this measure and note
that such a delay exists for all measures in the IPFQR Program.
However, we believe that the data will provide meaningful information
to consumers in making healthcare decisions because the data will be
able to reflect differences between IPFs in COVID-19 vaccination
coverage among HCP even if the data do not reflect immediate
vaccination rates.
Comment: Many commenters recommended that CMS reduce the mandatory
reporting frequency to quarterly or to annually to reduce reporting
burden for facilities. Some of these commenters stated that this
mirrors the reporting schedule for the Influenza Vaccination Coverage
Among HCP measure which is in some quality reporting programs.
Response: As we stated in the FY 2024 IPF PPS proposed rule (88 FR
21292), the measure developer noted that the model used for this
measure is based on the Influenza Vaccination Coverage Among HCP
measure (CBE #0431), and it intends to utilize a similar approach to
the modified COVID-19 Vaccination Coverage Among HCP measure if
vaccination strategy becomes seasonal. We continue to monitor COVID-19
as part of our public health response and will consider information we
collect to inform any potential action that may address seasonality in
future rulemaking.
Comment: Some commenters expressed concern that the COVID-19
Vaccination Coverage Among HCP measure has not been endorsed by the
CBE.
Response: The current version of the measure received CBE
endorsement (CBE #3636, ``Quarterly Reporting of COVID-19 Vaccination
Coverage Among Healthcare Personnel'') on July 26, 2022. As we stated
in the FY 2024 IPF PPS proposed rule (88 FR 21292 through 21293), in
the case of a specified area or medical topic
[[Page 51133]]
determined appropriate by the Secretary for which a feasible and
practical measure has not been endorsed by the entity with a contract
under section 1890(a) of the Act, the Secretary may specify a measure
that is not so endorsed as long as due consideration is given to
measures that have been endorsed or adopted by a consensus organization
identified by the Secretary. As discussed in section V.E.2.b. of the
proposed rule (88 FR 21292 through 21293) and this final rule, we
reviewed measures endorsed by consensus organizations and were unable
to identify any other measures on this topic endorsed by a consensus
organization; therefore, we believe the exception for non- CBE-
endorsed measures applies. The measure steward, CDC, is currently
pursuing endorsement for the modified version of the measure as the
current version of the measure has already received endorsement.
Comment: Some commenters recommended that CMS include an exclusion
for sincerely held religious beliefs to adhere to HHS Office of Civil
Rights Guidance. Some of these commenters also requested the measure be
updated to track the number of HCP who decline vaccination. Several
commenters stated that there are many factors beyond an IPF's control
(such as weather, holidays, vaccine supply, etc.) that may affect
performance on this measure.
Response: We recognize that there are many reasons, including
religious objections or concerns regarding an individual HCP's specific
health status which may lead individual HCP to decline vaccination. The
CDC's NHSN tool allows facilities to report on the number of HCP who
were offered a vaccination but declined for religious or philosophical
objections.\244\ We understand the commenters' concern that there are
many factors outside of an IPF's control that could affect vaccination
coverage; however, we believe that all IPFs face such concerns and that
public reporting of these data can help patients and their caregivers
identify which IPFs have better vaccination coverage among their HCP.
Furthermore, we believe that reporting of the measure based on one week
per month over three months will allow some seasonal or other effects
to be mitigated. We wish to emphasize that neither the modified measure
nor the current version of the measure mandate vaccines. The COVID-19
Vaccination Coverage Among HCP measure only requires reporting of
vaccination rates for successful program participation.
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\244\ https://www.cdc.gov/nhsn/forms/COVIDVax.HCP_.FORM_May2022-508.pdf.
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Final Decision: After consideration of the public comments we
received, we are finalizing modification of the COVID-19 Vaccination
Coverage Among HCP measure as proposed.
F. Removal or Retention of IPFQR Program Measures
1. Background
In the FY 2018 IPPS/LTCH PPS final rule (82 FR 38463 through 38465)
and FY 2019 IPF PPS final rule (83 FR 38591 through 38593), we adopted
several considerations for removing or retaining measures within the
IPFQR Program.
Specifically, we have adopted eight factors that we consider when
evaluating whether to propose a measure for removal from the IPFQR
Program. These factors are: (1) measure performance among IPFs is so
high and unvarying that meaningful distinctions and improvements in
performance can no longer be made (``topped out'' measures); (2)
measure does not align with current clinical guidelines or practice;
(3) measure can be replaced by a more broadly applicable measure
(across setting or populations) or a measure that is more proximal in
time to desired patient outcomes for the particular topic; (4) measure
performance or improvement does not result in better patient outcomes;
(5) measure can be replaced by a measure more strongly associated with
desired patient outcomes for the particular topic; (6) measure
collection or public reporting leads to negative intended consequences
other than patient harm; (7) measure is not feasible to implement as
specified; and (8) the costs associated with a measure outweigh the
benefit of its continued use in the program. For measure removal factor
one, we specified that a measure is ``topped out'' if it meets the
following criteria: (1) statistically indistinguishable performance at
the 75th and 90th percentiles; and (2) the truncated coefficient of
variation is less than or equal to 0.10.
We also adopted three factors for consideration in determining
whether to retain a measure in the IPFQR Program, even if the measure
meets one or more factors for removal. These retention factors are: (1)
measure aligns with other CMS and HHS policy goals, such as those
delineated in the National Quality Strategy and CMS Quality Strategy;
(2) measure aligns with other CMS programs, including other quality
reporting programs; and (3) measure supports efforts to move IPFs
towards reporting electronic measures. In the FY 2018 IPPS/LTCH PPS
final rule (82 FR 38464), we stated that these removal and retention
factors are considerations that we consider in balancing the benefits
and drawbacks of removing or retaining measures on a case-by-case
basis.
Since adoption, we have not proposed any changes to these policies
for removal or retention and refer readers to the FY 2018 IPPS/LTCH PPS
final rule (82 FR 38463 through 38465) and the FY 2019 IPF PPS final
rule (83 FR 38591 through 38593) for more information. We did not
propose any updates to these measure retention and removal policies. We
proposed to codify these previously adopted policies at Sec.
412.433(e).
We welcomed comments on this proposal.
Comment: One commenter recommended an additional factor, relevance
and importance of the measure to patients, for CMS to consider when
deciding whether to remove or modify a measure in the IPFQR. The
commenter stated this was consistent with TEPs which inform the measure
development process and would improve the patient centeredness of the
program.
Response: We appreciate this recommendation and will consider it in
the future as we continue to evaluate all elements of the IPFQR
Program.
Final Decision: After consideration of the public comments we
received, we are finalizing codification of our measure retention and
removal policies as proposed.
2. Measures for Removal
We continue to evaluate our measure set against these removal and
retention factors on an ongoing basis. In this continual evaluation of
the IPFQR Program measure set under our Meaningful Measures Framework
and according to our measure removal and retention factors, we
identified two measures that we believe are appropriate to remove from
the IPFQR Program beginning with the FY 2025 payment determination. Our
discussion of these measures follows.
a. Removal of the Patients Discharged on Multiple Antipsychotic
Medications With Appropriate Justification (HBIPS-5) (Previously
Endorsed Under CBE #0560) Measure Beginning With FY 2025 Payment
Determination
[[Page 51134]]
As we assessed our existing measure set to ensure that it remains
appropriate for the IPFQR Program, we determined that measure removal
factor two (that is, measure does not align with current clinical
guidelines or practice) applies to the Patients Discharged on Multiple
Antipsychotic Medications with Appropriate Justification (HBIPS-5) (CBE
#560) measure due to the American Psychiatric Association's (APA's)
updated guidelines for patients with schizophrenia.
We adopted the HBIPS-5 measure in the FY 2013 IPPS/LTCH PPS final
rule as part of a set with the Patients Discharged on Multiple
Antipsychotic Medications (HBIPS-4) (previously endorsed under CBE
#0552) measure because of the belief that these two measures would help
reduce unnecessary use of multiple antipsychotics, which would lead to
better clinical outcomes and reduced side effects for patients (77 FR
53649 through 53650). We subsequently removed the HBIPS-4 measure in
the FY 2016 IPF PPS final rule (80 FR 46695 through 46696). As we
described in that final rule, following our adoption of these measures,
some experts, including the CBE, provided input that the HBIPS-4
measure did not provide meaningful information about the quality of
care received by IPF patients. This led to the removal of the HBIPS-4
measure's CBE endorsement in January 2014. During the CBE's review of
the HBIPS-4 measure in 2014, the CBE observed that the HBIPS-4 and
HBIPS-5 measures could be collected and reported separately and
expressed that the HBIPS-5 measure should be retained in the IPFQR
Program as it continued to provide meaningful quality of care
information (80 FR 046695 through 46696).
Evidence supporting development and adoption of the HBIPS-5 measure
included the APA Workgroup on Schizophrenia's 2004 Practice Guideline
for the Treatment of Patients with Schizophrenia. These guidelines
stated that the ``combinations of antipsychotics . . . should be
justified by strong documentation that the patient is not equally
benefited by monotherapy.'' \245\ In December 2019, the APA Board of
Trustees approved updated guidelines for treatment of patients with
schizophrenia.\246\ The updated guidelines are based on evolving
clinical knowledge and have increased focus and specificity of
recommendations for the use of pharmacotherapy; they also underscore
the importance of patient preference and shared-decision making.\247\
These guidelines no longer contain the recommendation that combinations
of antipsychotics should be justified by strong documentation that
patients are not equally benefited by monotherapy. Therefore, the
guidelines that originally supported the HBIPS-5 measure have changed
substantially, and the HBIPS-5 measure is no longer aligned with
current clinical guidelines and practice.
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\245\ https://www.researchgate.net/publication/298561608_Practice_guideline_for_the_treatment_of_patients_with_schizophrenia_second_edition.
\246\ https://ajp.psychiatryonline.org/doi/10.1176/appi.ajp.2020.177901.
\247\ The American Psychiatric Association. Practice Guideline
for the Treatment of Patients with Schizophrenia, Third Edition.
Available at: https://psychiatryonline.org/doi/book/10.1176/appi.books.9780890424841. Accessed on February 15, 2023.
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Furthermore, the HBIPS-5 measure is no longer supported by the
measure steward (that is, The Joint Commission), who withdrew it from
the CBE endorsement process in 2019. As a result, the HBIPS-5 measure
lost its CBE endorsement in October 2019.\248\ Subsequent to this, the
CBE-convened MAP's discussion of measure set removal for 2021-2022
included a discussion of this measure. Because the HBIPS-5 measure no
longer aligns with clinical guidelines and is no longer CBE endorsed
due to lack of support from the measure developer, the MAP recommended
that the measure should be removed from the IPFQR Program.\249\
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\248\ CMS Measures Inventory Tool. Patients Discharged on
multiple antipsychotic medications with appropriate justification.
Available at: https://cmit.cms.gov/cmit/#/MeasureView?variantId=1141§ionNumber=1.
\249\ MAP 2021-2022 Considerations for Implementing Measures in
Federal Programs. Available at: https://mmshub.cms.gov/sites/default/files/map_2021-2022_considerations_for_implementing_measures_in_federal_programs_final_report.pdf.
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We agree with the MAP's assessment that the measure no longer
aligns with clinical guidelines and therefore proposed to remove the
measure from the IPFQR Program beginning with the FY 2025 payment
determination. We note that data for the FY 2024 payment determination
represents care provided in CY 2022 and will be reported to CMS prior
to the publication of this FY 2024 IPF PPS final rule; therefore, the
FY 2025 payment determination is the first period for which we can
remove this measure.
We invited comments on our proposal.
Comment: Many commenters supported removing HBIPS-5 from the IPFQR
Program. These commenters agreed that the measure no longer aligns with
the updated clinical guidance from the APA.
Response: We thank these commenters for their support.
Comment: Several commenters expressed concern about the long-term
effects of psychotropic medications, especially antipsychotics, and
recommended that CMS defer removal until additional research can be
performed to ensure there are minimal long-term effects of
antipsychotic medications.
Response: We appreciate commenters' concern about the long-term
effects of psychotropic medications. We note that our proposed removal
of the measure was based on the updated APA guidelines for treatment of
patients with schizophrenia. These guidelines underwent a rigorous
review process prior to being updated, which included a review of the
benefits and harms of each treatment.\250\
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\250\ https://www.psychiatry.org/File%20Library/Psychiatrists/Practice/Clinical%20Practice%20Guidelines/Guideline-Development-Process.pdf.
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Final Decision: After consideration of the public comments we
received, we are finalizing removal of the Patients Discharged on
Multiple Antipsychotic Medications with Appropriate Justification
(HBIPS-5) measure as proposed.
b. Removal of the Tobacco Use Brief Intervention Provided or Offered
and Tobacco Use Brief Intervention (TOB-2/2a) Measure Beginning With
the FY 2025 Payment Determination
We adopted the Tobacco Use Brief Intervention Provided or Offered
and Tobacco Use Brief Intervention (TOB-2/2a) measure in the FY 2015
IPF PPS final rule (79 FR 45971 through 45972) because of our belief
that it is important to address the common comorbidity of tobacco use
among IPF patients. The TOB-2/2a measure requires IPFs to chart-
abstract measure data on a sample of IPF patient records, in accordance
with established sampling policies (80 FR 46717 through 46719). When we
introduced the TOB-2/2a measure to the IPFQR Program, the benefits of
this measure were high because IPF performance was not consistent with
respect to, and there were no other measures addressing, provision of
tobacco use cessation counseling or treatment. At the time, the TOB-2/
2a measure provided a means of distinguishing IPF performance
regarding, and incentivized facilities to improve rates of, treatment
for this common comorbidity. To further address tobacco use, we
subsequently adopted the Tobacco Use Treatment Provided or Offered at
Discharge and
[[Page 51135]]
Tobacco Use Treatment at Discharge (TOB-3/3a) measure in the FY 2016
IPF PPS final rule (80 FR 46696 through 46699).
In the FY 2022 IPF PPS proposed rule, we proposed to remove the
Tobacco Use Brief Intervention Provided or Offered and Tobacco Use
Brief Intervention (TOB-2/2a) measure from the IPFQR Program beginning
with the FY 2024 payment determination under our measure removal factor
8, the costs associated with a measure outweigh the benefit of its
continued use in the program (86 FR 19508 through 19509). We expressed
our belief that the quality improvement benefits from the TOB-2/2a
measure had greatly diminished because performance had leveled off,
that is overall performance on the measure was no longer improving. We
took this to mean that most IPFs routinely offer tobacco use brief
interventions.
In the FY 2022 IPF PPS proposed rule, we also expressed our belief
that the costs of maintaining this measure are high because costs are
multi-faceted and include not only the IPFs' burden associated with
reporting, but also our costs associated with implementing and
maintaining the measure (86 FR 19508 through 19509). Additionally, we
must expend resources in maintaining information collection systems,
analyzing reported data, and providing public reporting of the
collected information. We expressed that, for this measure, IPF
information collection burden and related costs associated with
reporting this measure to CMS were high because the measure is a chart-
abstracted measure. Furthermore, we observed CMS incurs costs
associated with the program oversight of the measure for public
display.
However, in the FY 2022 IPF PPS final rule, we did not finalize our
proposal to remove the Tobacco Use Brief Intervention Provided or
Offered and Tobacco Use Brief Intervention (TOB-2/2a) measure (86 FR
42648 through 42651). We stated that, following review of the public
comments we received, we believed the benefits of continuing to
encourage facilities to offer tobacco use brief interventions were
greater than we had estimated. We noted that these benefits included
the potential for IPFs to continue improving performance on the TOB-2/
2a measure, the importance of tobacco use interventions due to
increased tobacco use during the COVID-19 pandemic, and this measure's
potential influence on other quality improvement activities related to
tobacco use.
In our continual evaluation of the IPFQR Program measure set under
our Meaningful Measures Framework and according to our measure removal
and retention factors, we observed that having two measures addressing
tobacco use, which are both associated with relatively high information
collection burden, may not appropriately balance costs and benefits
within the program. While we believe that both the TOB-2/2a measure and
the TOB-3/3a measure address clinically important interventions to
address smoking in this population, we believe that the overall cost
associated with retaining both of these measures outweighs the benefit
of having two measures to address treatment for the same comorbidity
among the same patient population.
Both measures capture information about tobacco cessation
counseling and FDA-approved tobacco cessation medications. The
difference between the measures is that the TOB-2/2a measure captures
whether the tobacco cessation counseling and FDA-approved tobacco
cessation medications were offered or refused during the inpatient
stay, while the TOB-3/3a measure captures whether a referral to
outpatient tobacco cessation counseling and FDA-approved tobacco
cessation medications were offered or refused at the time of the
patient's discharge.
As we considered each of these measures, we determined that it
would be more appropriate to retain the TOB-3/3a measure in the IPFQR
Program, that is, to remove the TOB-2/2a measure instead of the TOB-3/
3a measure, because there is more opportunity for improvement on the
TOB-3/3a measure. Specifically, the performance on the TOB-3/3a measure
is lower than performance on the TOB-2/2a measure. National performance
on TOB-2 and 2a measure and TOB-3 and 3a measure for the last five
payment determination years in the IPFQR Program is presented in Table
19. Given the relatively high performance on the TOB-2/2a measure
compared to the TOB-3/3a measure, we believe that retaining the TOB-3/
3a measure, and removing the TOB-2/2a measure, would provide more
opportunity to drive improvement among IPFs; therefore, would
potentially impact more patients.
[GRAPHIC] [TIFF OMITTED] TR02AU23.023
As described earlier in this section VI.F.2.b of this final rule,
because the TOB-2/2a measure has a high cost (especially due to its
high information collection burden), we believe that these high costs
are no longer greater than the benefits of retaining this measure.
Therefore, we believe measure removal factor 8 (that is, the costs
associated with a measure outweigh the benefit of its continued use in
the IPFQR Program), applies to the TOB-2/2a measure.
Furthermore, the TOB-2/2a measure is no longer supported by the
measure steward (that is, The Joint Commission), who withdrew it from
the CBE endorsement process in 2018. Therefore, the TOB-2/2a measure
has not been CBE endorsed since October 2018.\251\
[[Page 51136]]
Subsequent to this, the CBE-convened MAP's discussion of measure set
removal for 2021and 2022 included a discussion of this measure. Because
the TOB-2/2a measure is a high-cost measure and is no longer CBE
endorsed, the MAP recommended that we remove the measure from the IPFQR
Program.\252\
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\251\ CMS Measures Inventory Tool. Tobacco Use Treatment
Provided or Offered. Available at: https://cmit.cms.gov/cmit/#/MeasureView?variantId=1818§ionNumber=1.
\252\ MAP 2021-2022 Considerations for Implementing Measures in
Federal Programs. Available at: https://mmshub.cms.gov/sites/default/files/map_2021-2022_considerations_for_implementing_measures_in_federal_programs_final_report.pdf.
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We agree with the MAP that this is a high-cost measure.
Furthermore, we recognize that it is similar to the other tobacco use
measure in the IPFQR Program measure set (that is, the TOB-3/3a
measure) which we did not propose to remove. Therefore, we proposed to
remove Tobacco Use Brief Intervention Provided or Offered and Tobacco
Use Brief Intervention (TOB-2/2a) measure under our measure removal
factor 8, ``the costs associated with a measure outweigh the benefit of
its continued use in the program,'' beginning with FY 2025 payment
determination. We note that data for the FY 2024 payment determination
represents care provided in CY 2022 and will be reported to CMS prior
to the publication of this FY 2024 IPF PPS final rule; therefore, the
FY 2025 payment determination is the first period for which we can
remove this measure.
We invited public comment on this proposal.
Comment: Many commenters supported removal of the TOB-2/2a measure
because it will reduce burden with minimal impact on patient outcomes
due to the retention of the TOB-3/3a measure. Some of these commenters
stated that the TOB-3/3a measure has more room for improvement and is
more likely to lead to improved patient outcomes.
Response: We thank these commenters for their support.
Comment: Many commenters opposed removal of the TOB-2/2a measure.
These commenters stated that tobacco use is a common comorbidity among
this patient population that leads to negative long-term health
outcomes. These commenters expressed that the TOB-2/2a and TOB-3/3a
measures both address important interventions to reduce tobacco use and
therefore recommended retaining both measures. Some of these commenters
expressed concern that, without the TOB-2/2a measure, IPFs will not
offer tobacco use interventions in the inpatient setting which
represents a missed opportunity to increase the likelihood that these
patients will quit using tobacco. Some of these commenters stated that
there is still room for improvement on the TOB-2/2a measure.
Response: We agree with commenters that tobacco use is a common
comorbidity among this patient population that leads to negative long-
term health outcomes. We remain committed to the screening, counseling
and provision of smoking intervention services in this population of
patients. We note that studies have demonstrated that during the acute
hospital stay, there is no statistically significant increase in
smoking cessation for non-intensive counseling interventions, such as
brief intervention,\253\ which is what TOB-2/2a measures. We will
retain TOB-3/3a which focuses on the provision of smoking cessation
referral and treatment for smoking cessation at discharge, to be
continued in the ambulatory setting, which studies have shown a greater
benefit to the patient. Even though we are finalizing the removal of
the TOB-2/2a measure, and therefore IPFs and IPFs will no longer be
required to collect and submit TOB-2/2a data to CMS, IPFs are still
encouraged to continue to provide smoking cessation counseling and
brief interventions during the psychiatric stay as determined
appropriate by the patient's provider and patient. We appreciate
commenters concerns and will continue to monitor whether additional
measures related to smoking cessation and/or intensive behavioral
counseling are necessary. We also support the extensive other work that
is being done by HHS and the broader Administration to reduce smoking,
including the framework proposed by the Office of the Assistant
Secretary for Health (OASH) (88 FR 42377).
---------------------------------------------------------------------------
\253\ : Rigotti NA, Clair C, Munaf[ograve] MR, Stead LF.
Interventions for smoking cessation in hospitalised patients.
Cochrane Database Syst Rev. 2012 May 16;5(5):CD001837. doi: 10.1002/
14651858.CD001837.pub3. PMID: 22592676; PMCID: PMC4498489. Available
at:: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498489/.
---------------------------------------------------------------------------
We agree with commenters that TOB-2/2a and TOB-3/3a both address
important interventions (that is, tobacco use treatment brief
intervention provided or offered during the inpatient stay and tobacco
use treatment provided or offered at discharge) and that there is still
room for improvement for both measures. While it is possible that,
without the TOB-2/2a measure, some IPFs may stop providing inpatient
tobacco use interventions prior to during the patient's discharge
planning, we continue to believe that the benefit of having two
measures to address this comorbidity does not outweigh the significant
reporting burden for IPF's associated with these specific measures. We
note that we believe that the benefits of tobacco use interventions
during the inpatient stay are high; however, we do not believe the
benefits of measuring these interventions along with similar
interventions at discharge are sufficiently high to outweigh the
burden.
Final Decision: After consideration of the public comments we
received, we are finalizing removal of the Tobacco Use Brief
Intervention Provided or Offered and Tobacco Use Brief Intervention
measure as proposed.
G. Summary of IPFQR Program Measures
1. IPFQR Program Measures for the FY 2024 Payment Determination
We did not propose any changes to our measure set for the FY 2024
payment determination. The 14 measures which will be in the program for
FY 2024 payment determination are shown in Table 20.
[[Page 51137]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.024
2. IPFQR Program Measures for the FY 2025 Payment Determination
In this final rule. we are removing two measures for the FY 2025
payment determination and subsequent years. We also are modifying one
measure for the FY 2025 payment determination and subsequent years. The
12 measures, which will be in the program for FY 2025 payment
determination are shown Table 21.
[[Page 51138]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.025
3. IPFQR Program Measures for the FY 2026 Payment Determination
The measure set for FY 2026 payment determination and subsequent
years will include 13 mandatory and two voluntary measures. This
includes the 12 mandatory measures listed in Table 21 of this final
rule for the FY 2025 payment determination and subsequent years, as
well as the one mandatory measure and two voluntary measures we adopted
for the FY 2026 payment determination and subsequent years. The
measures which will be in the program for FY 2026 payment determination
are shown Table 22.
[[Page 51139]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.026
4. IPFQR Program Measures for the FY 2027 IPFQR Program's Payment
Determination
The measure set for the FY 2027 payment determination and
subsequent years, will include 15 mandatory measures and one voluntary
measure. This includes the 13 mandatory measures listed in Table 22 of
this final rule for the FY 2026 payment determination and subsequent
years, as well as the two measures which we are requiring for the FY
2027 payment determination and subsequent years. It also includes the
one new voluntary measure adopted in section VI.D.5 of this final rule.
The measures which we are finalizing for the FY 2027 payment
determination and subsequent years are shown Table 23.
[[Page 51140]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.027
5. IPFQR Program Measures for the FY 2028 Payment Determination
The measure set for the FY 2028 payment determination and
subsequent years will include 16 mandatory measures. This includes the
15 mandatory measures listed in Table 23 of this final rule for the FY
2027 payment determination as well as the measure which we finalized
beginning with the FY 2028 payment determination. The measures which
will be in the program beginning with the FY 2028 payment determination
are shown Table 24.
[[Page 51141]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.028
H. Public Display and Review Requirements
In the FY 2013 IPPS/LTCH PPS final rule (77 FR 53653 through
53654), we adopted procedures for making data submitted under the IPFQR
Program available to the public, after an IPF has the opportunity to
review such data prior to public display, as required by section
1886(s)(4)(E) of the Act. We adopted modifications to these procedural
requirements in the FY 2014 IPPS/LTCH PPS final rule (78 FR 50897
through 50898), and the FY 2017 IPPS/LTCH PPS final rule (81 FR 57248
through 57249).
Specifically, the IPFQR Program adopted a policy to provide IPFs a
30-day period to review their data, and submit corrections to errors
resulting from CMS calculations, prior to public display on a CMS
website. The IPFQR Program notifies IPFs of the exact timeframes for
this preview period and public display through subregulatory guidance.
We did not propose any changes to these requirements.
We proposed to codify the procedural requirements for public
reporting of IPFQR Program data at Sec. 412.433(g). If finalized,
paragraph (g) would provide that IPFs will have a period of 30 days
[[Page 51142]]
to review data on quality measures that CMS received under the IPFQR
Program, and submit corrections to errors resulting from CMS
calculations, prior to CMS publishing this data on a CMS website.
We welcomed comments on our proposal to codify these policies.
We did not receive any comments on this proposal.
Final Decision: We are finalizing codification of these policies.
I. Form, Manner, and Timing of Quality Data Submission for the FY 2024
Payment Determination and Subsequent Years
1. Procedural Requirements for the FY 2024 Payment Determination and
Subsequent Years
We refer readers to the FY 2013 IPPS/LTCH PPS final rule (77 FR
53654 through 53655), the FY 2014 IPPS/LTCH PPS final rule (78 FR 50898
through 50899), the FY 2018 IPPS/LTCH PPS final rule (82 FR 38471
through 38472), and the FY 2022 IPF PPS final rule (86 FR 42656 through
42657) for our previously finalized procedural requirements for
participation in, and withdrawal from, the IPFQR Program, as well as
data submission requirements. We did not propose any changes to our
previously finalized procedural requirements.
We proposed to codify these procedural requirements for
participation in the IPFQR Program at Sec. 412.433(b) through (d).
Paragraphs (b) through (d) will set forth the procedural requirements
for an IPF to register for, or withdraw from, participation in the
IPFQR Program and to submit the required data on measures in a form and
manner and time specified by CMS.
We welcomed comments on our proposal to codify these policies.
We did not receive any comments on this proposal.
Final Decision: We are finalizing codification of the procedural
requirements for participation in the IPFQR Program at Sec. 412.433(b)
through (d). We are finalizing the regulation text as proposed except
to replace references to ``QualityNet'' with ``CMS-designated
information system'' and update the description of the registration
process because we inadvertently referred to QualityNet in the proposed
rule. We have migrated to a new internet system for many quality
reporting programs, and we use the term ``CMS-designated information
system'' to refer both to that system and any future updates to it.
2. Data Submission Requirements for the FY 2025 Payment Determination
and Subsequent Years
We refer readers to the FY 2013 IPPS/LTCH PPS final rule (77 FR
53655 through 53657), the FY 2014 IPPS/LTCH PPS final rule (78 FR 50899
through 50900), the FY 2018 IPPS/LTCH PPS final rule (82 FR 38472
through 38473), and the FY 2022 IPF PPS final rule (86 FR 42657 through
42661) for our previously finalized data submission requirements.
The measure we are modifying beginning with the FY 2025 payment
determination--the COVID-19 Vaccination Coverage Among HCP measure--
requires facilities to report data on the number of HCP who have
received a complete vaccination course of a COVID-19 vaccine through
the Centers for Disease Control and Prevention's (CDC's) National
Healthcare Safety Network (NHSN). We are updating this measure to no
longer refer to ``complete vaccination course'' but instead to refer to
``up-to-date'' vaccination, as described in section VI.E. of this final
rule.
We did not propose any updates to the form, manner, and timing of
data submission for the COVID-19 Vaccination Coverage Among HCP measure
and refer readers to the FY 2022 IPF PPS final rule (86 FR 42657) for
these policies.
3. Data Submission Requirements for the FY 2026 Payment Determination
and Subsequent Years
In sections VI.D 3 and VI.D.4 of this final rule, we are adopting
measures for voluntary reporting for the FY 2026 IPFQR Program and
mandatory reporting for the FY 2027 IPFQR Program's payment
determination and subsequent years. These measures are the Screening
for Social Drivers of Health measure and Screen Positive Rate for
Social Drivers of Health measure. We proposed that our previously
finalized data submission requirements, specifically, our previously
finalized data submission requirements for aggregate data reporting
described in the FY 2018 IPPS/LTCH PPS final rule (82 FR 38472 through
38473) would apply to these measures.
We invited public comment on our proposal.
We did not receive any public comments on this proposal.
Final Decision: We are finalizing our proposal for data submission
requirements for the FY 2026 payment determination and subsequent
years.
4. Data Submission Requirements for the FY 2027 Payment Determination
and Subsequent Years
In section VI.D.5. of this final rule, we are adopting one patient-
reported measure, Psychiatric Inpatient Experience (PIX) measure for
voluntary reporting beginning with the CY 2025 performance period (the
data for which will be submitted to CMS during CY 2026) and mandatory
reporting beginning with the FY 2028 payment determination (that is,
data from the CY 2026 performance period submitted to CMS during CY
2027). Because, unlike other patient experience of care measures, this
measure is collected by facilities prior to discharge, we proposed that
facilities would report these data using the patient-level data
reporting described in the FY 2022 IPF PPS final rule (86 FR 42658
through 42661).
We invited public comment on our proposal.
We did not receive any public comments on this proposal.
Final Decision: We are finalizing our proposal for data submission
requirements for the FY 2027 payment determination and subsequent
years. We note that reporting these data will be voluntary for the FY
2027 payment determination and will be mandatory beginning with the FY
2028 payment determination.
5. Data Validation Pilot Beginning With Data Submitted in CY 2025
As discussed in the FY 2019 IPF PPS final rule (83 FR 28607) and in
the FY 2022 IPF PPS final rule (86 FR 42661), we are concerned that the
ability to detect error is lower for aggregate measure data reporting
than for patient-level data reporting (that is, data regarding each
patient included in a measure and, for example, whether the patient was
included in the numerator and denominator of the measure). In the FY
2022 IPF PPS final rule, we noted that adoption of patient-level data
requirements would enable us to adopt a data validation policy for the
IPFQR Program in the future (86 FR 42661). We believe that it would be
appropriate to develop such a policy incrementally through adoption of
a data validation pilot prior to national implementation of data
validation within the IPFQR Program. We sought public input on a
potential data validation pilot, and many commenters supported the
concept of data validation following implementation of patient-level
reporting (86 FR 42661). In the FY 2022 IPF PPS final rule, we adopted
mandatory patient-level reporting
[[Page 51143]]
beginning with data submitted in CY 2023 affecting the FY 2024 payment
determination and reflecting care provided during CY 2022 (86 FR 42658
through 42661).
We are now finalizing a data validation pilot beginning with data
submitted in CY 2025 (reflecting care provided during CY 2024). When we
sought public comment on a data validation pilot in the FY 2022 IPF PPS
proposed rule (86 FR 19515), we requested input on potential elements
of such a pilot, including the number of measures and the number of
participating IPFs. As summarized in the FY 2022 IPF PPS final rule (86
FR 42661), one commenter recommended selecting two measures and 200
IPFs for this pilot. We considered that recommendation; however, to
align with validation policies in our other quality reporting programs,
we decided to request a specific number of charts. Specifically, we
proposed to request eight charts per quarter from each IPF as opposed
to requesting all of the charts that each facility used to calculate
one or more specific measures. We also decided to initiate our pilot
with fewer IPFs than the commenter recommended to limit the burden
associated with this pilot.
We also reviewed the validation policies of other quality reporting
programs. We specifically reviewed the Hospital IQR Program's chart-
abstracted measure validation policies described in the FY 2017 IPPS/
LTCH PPS final rule (81 FR 57179 through 57180), the Hospital IQR
Program's pilot for eCQM validation described in the FY 2015 IPPS/LTCH
PPS final rule (79 FR 50262 through 50273), the Hospital Outpatient
Quality Reporting (OQR) Program's planned pilot of data validation as
described in the CY 2009 OPPS/ASC final rule (73 FR 68502), and the
Hospital OQR Program's finalized validation policies as described in
the CY 2012 OPPS/ASC final rule (76 FR 74485) and the CY 2018 OPPS/ASC
final rule (82 FR 59441 through 5944) because these programs are also
pay-for-reporting programs, like the IPFQR Program.
Following our review of the validation policies within these
programs, we proposed a validation pilot in which we would randomly
select on an annual basis up to 100 IPFs and request each selected IPF
to provide to CMS eight charts per quarter, a total of 32 charts per
year, used to calculate all chart-based measures beginning with data
submitted in CY 2025. We believe that randomly selecting up to 100 IPFs
would provide a sufficiently large set of IPFs to meaningfully test our
validation procedures while minimizing burden for IPFs. We will specify
the timeline and mechanism for submitting data in our data requests to
individual IPFs that have been selected to participate in the
validation pilot. We note that consistent with the Hospital IQR
Program, we will reimburse IPFs for the cost of submitting charts for
validation at a rate of $3.00 per chart (85 FR 58949).
Because this is a voluntary pilot, we recognize that some selected
IPFs will not participate; however, we believe that this pilot would be
beneficial for IPFs that do participate as an opportunity to receive
education and feedback on the data they submit prior to future proposal
and adoption of a validation requirement in the IPFQR Program.
We invited comments on our proposal.
Comment: Several commenters expressed support for the data
validation pilot.
Response: We thank these commenters for their support.
Comment: Several commenters provided recommendations for the data
validation pilot. One commenter suggested allowing participants to opt
into the pilot as opposed to selecting potential participants. One
commenter requested that CMS ensure that the individuals doing the data
validation have clinical expertise in the psychiatric setting to ensure
appropriate interpretation of data. Another commenter recommended that
CMS complete the pilot and analyze the data generated by the pilot
prior to proposing and adopting a full data validation program.
Response: We thank these commenters for their input. We note that
the data validation pilot described in this section is based on
validation programs in other quality reporting programs. We believe
that selecting IPFs to participate will allow us to test our processes
for selection and notification and therefore we believe that this will
be a more effective test than allowing IPFs to opt into the pilot. We
note that participation in the data validation pilot will be voluntary
for the IPFs which we select. We will consider recommendations for
qualifications for personnel to perform the data validation and for
analysis of the results as we implement this program. We believe it is
appropriate to develop a data validation policy incrementally through
adoption of a data validation pilot prior to national implementation of
data validation within the IPFQR Program. We intend to analyze data
collected through this data validation pilot to inform development of a
future nationally implemented data validation program. We note that
while we will analyze data collected through the data validation pilot
in developing the program for national implementation, the pilot will
be ongoing until national implementation so that we can continue to
collect data and IPFs can continue to receive education and feedback on
the data they submit.
Comment: One commenter expressed that a data validation pilot with
payment ramifications is premature because patient-level data
submission is still new to the IPFQR Program, because CMS has not
sufficiently defined the pilot elements, and because it is unclear that
there would be auditors with sufficient clinical expertise. Another
commenter recommended that CMS use the data in the future IPF patient
assessment instrument (PAI) to validate quality measure data. Another
commenter recommended postponing this pilot until the financial and
staffing shortages caused by the COVID-19 pandemic have been resolved.
Response: We note that the participation in the data validation
pilot is voluntary, and that IPFs will not receive any payment
penalties during the data validation program's pilot period. With
respect to the future IPF PAI, we will consider the potential interplay
between data elements included in the PAI and IPFQR Program quality
measure data for validation purposes, but believe those considerations
are premature as a PAI has not yet been implemented for the IPF
setting. Finally, we recognize that healthcare providers, including
IPFs, are still recovering from the effects of the COVID-19 pandemic,
but note that participation in the data validation pilot is voluntary.
Comment: One commenter stated that the reimbursement rate of $3.00/
chart is insufficient to cover the time and materials associated with
participating in the pilot.
Response: We understand the commenters concern that $3.00/chart may
not cover the time and materials associated with participating in the
pilot. We note that this reimbursement is consistent with the
reimbursement rates for submitting charts for validation in other
quality reporting programs. However, we intend to use the pilot program
to identify potential modifications prior to adopting a full validation
program. We will consider the appropriateness of our reimbursement at
that time.
Final Decision: After consideration of the public comments we
received, we are finalizing our data validation pilot as proposed.
[[Page 51144]]
6. Quality Measure Sampling Requirements
We refer readers to the FY 2013 IPPS/LTCH PPS final rule (77 FR
53657 through 53658), the FY 2014 IPPS/LTCH PPS final rule (78 FR 50901
through 50902), the FY 2016 IPF PPS final rule (80 FR 46717 through
46719), and the FY 2019 IPF PPS final rule (83 FR 38607 through 38608)
for discussions of our previously finalized sampling policies.
Because the Facility Commitment to Health Equity measure proposed
in section VI.D.2 of this final rule is a structural attestation
measure, these policies do not apply to that measure. Additionally,
because the Screening for Social Drivers of Health measure (described
in section VI.D.3 of this final rule) applies to all patients and the
Screen Positive Rate for Social Drivers of Health measure (described in
section VI.D.4 of this final rule) applies to all patients who have
been screened for health-related social needs (HRSNs), our previously
finalized sampling policies would not apply to these two measures. As
described in the FY 2022 IPF PPS final rule, our sampling policies do
not apply to the COVID-19 Vaccination Coverage Among Healthcare
Personnel measure because the denominator is all healthcare personnel
(86 FR 42661).
Generally, we have applied our sampling procedures to chart-
abstracted measures, where appropriate (that is, where the measure does
not require application to the entire patient population). However,
because the PIX survey measure is a patient reported measure, we have
considered whether our sampling procedures for chart-abstracted
measures are appropriate for this measure. After consideration of our
current sampling procedures and sampling for patient reported measures
in other quality reporting programs (specifically, the requirements for
reporting the HCAHPS measure), we proposed that the PIX survey measure
(described in section VI.D.5 of this final rule) would be eligible for
sampling but would not be included in the global sample. Instead, we
proposed that sampling for this measure would align with sampling for
the HCAHPS survey measure in acute care hospitals and the Hospital IQR
Program as described in the HCAHPS Quality Assurance Guidelines.\254\
Specifically, we proposed to require IPFs to develop sampling plans
that ensure that IPFs are able to submit data for 300 completed PIX
surveys per year. IPFs will be required to sample from every month
throughout the entire reporting period and not stop sampling or curtail
ongoing interview activities once a certain number of completed surveys
has been attained. IPFs that are unable to reach 300 completed surveys
through sampling will be required to submit data on survey results for
all eligible patient discharges.
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\254\ HCHAPS Quality Assurance Guidelines, Version 17.0. March
2022. Available at: https://hcahpsonline.org/globalassets/hcahps/quality-assurance/2022_qag_v17.0.pdf.
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We invited public comment on our proposal.
Comment: One commenter recommended allowing facilities to apply
their sampling methodologies to the Screening for Social Drivers of
Health measure and the Screen Positive Rate for Social Drivers of
Health measure to reduce burden.
Response: We acknowledge that applying sampling methodologies for
these two measures would impact abstraction and reporting burden. We
have proposed these measures to align with other quality reporting and
value-based purchasing programs (specifically, the Hospital IQR
Program) as well as the same measure proposals for the PPS-Exempt
Cancer Hospital Quality Reporting Program in the FY 2024 IPPS/LTCH PPS
proposed rule (88 FR 27122 through 27130) and the End-Stage Renal
Disease (ESRD) Quality Incentive Program in the CY 2024 ESRD
Prospective Payment System proposed rule (88 FR 42509 through 42518).
We note that the Hospital IQR Program adopted these two measures
without sampling in the FY 2023 IPPS/LTCH PPS final rule (87 FR 49191
through 49220). We believe that adopting these measures consistently
across programs will increase the cross-setting comparability of
measure results for the Screening for Social Drivers of Health measure;
provide more information regarding community needs for specific
communities that are served by multiple healthcare organizations for
the Screen Positive Rate for Social Drivers of Health measure; and
ensure that we are consistently conveying the importance of identifying
and addressing HRSNs across all settings.
Comment: Several commenters recommended that CMS establish a
statistically valid random sampling process for all IPFs to apply for
the PIX survey measure to ensure that selection bias does not occur.
Response: We will provide updated guidance for developing sampling
plans and other implementation guidance for the PIX survey measure.
This guidance will align with sampling guidance for the HCAHPS measure
in the Hospital IQR Program.
Comment: One commenter requested clarification regarding whether
all patients would be eligible for inclusion in the sample for the PIX
survey measure or only Medicare patients.
Response: To the extent feasible we believe that it is important to
include all patients in our quality reporting measures. While some
measures do not allow inclusion of all patients (specifically, measures
abstracted from Medicare claims data); there are no feasibility issues
which require the PIX survey measure to be limited to patients covered
by any specific payer. Therefore, all patients, regardless of payer,
are included in the population from which the sample for this measure
is selected.
Comment: One commenter requested clarification regarding whether
IPFs that were unable to reach 300 completed surveys would be
penalized.
Response: IPFs that are unable to reach 300 completed PIX surveys
because of the size or characteristics of their patient population
should submit data on all eligible patients. IPFs that meet this
requirement would not be penalized for not submitting data on 300
completed PIX surveys.
Final Decision: We are finalizing our proposals related to sampling
for the newly adopted measures.
7. Non-Measure Data Collection
We refer readers to the FY 2015 IPF PPS final rule (79 FR 45973),
the FY 2016 IPF PPS final rule (80 FR 46717), and the FY 2019 IPF PPS
final rule (83 FR 38608) for our previously finalized non-measure data
collection policies. We did not propose any changes to these policies.
8. Data Accuracy and Completeness Acknowledgement (DACA) Requirements
We refer readers to the FY 2013 IPPS/LTCH PPS final rule (77 FR
53658) for our previously finalized DACA requirements. We did not
propose any changes to these policies.
J. Reconsideration and Appeals Procedures
We refer readers to 42 CFR 412.434 for the IPFQR Program's
reconsideration and appeals procedures. We did not propose any changes
to these policies.
K. Extraordinary Circumstances Exceptions (ECE) Policy
We refer readers to the FY 2013 IPPS/LTCH PPS final rule (77 FR
53659 through 53660), the FY 2014 IPPS/LTCH PPS final rule (78 FR
50903), the FY 2015 IPF PPS final rule (79 FR 45978), and the FY 2018
IPPS/LTCH PPS final rule (82 FR 38473 through 38474) for our previously
finalized Extraordinary
[[Page 51145]]
Circumstances Exceptions policies. We did not propose any changes to
these policies.
We proposed to codify the ECE policies at Sec. 412.433(f). As
finalized, paragraph (f) provides that we may grant an exception to one
or more data submission deadlines and requirements in the event of
extraordinary circumstances beyond the control of the IPF either in
response to a request by the IPF or at our discretion if we determine
an extraordinary circumstance occurred.
We solicited comments on our proposal to codify these policies.
We did not receive any comments on this proposal.
Final Decision: We are finalizing our proposal to codify these
policies.
VII. Collection of Information Requirements
Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501 et
seq.), we are required to provide 30-day notice in the Federal Register
and solicit public comment before a ``collection of information''
requirement is submitted to the Office of Management and Budget (OMB)
for review and approval. For the purposes of the PRA and this section
of the preamble, collection of information is defined under 5 CFR
1320.3(c) of the PRA's implementing regulations.
To fairly evaluate whether an information collection should be
approved by OMB, section 3506(c)(2)(A) of the PRA requires that we
solicit comment on the following issues:
The need for the information collection and its usefulness
in carrying out the proper functions of our agency.
The accuracy of our estimate of the information collection
burden.
The quality, utility, and clarity of the information to be
collected.
Recommendations to minimize the information collection
burden on the affected public, including automated collection
techniques.
Our April 10, 2023 (88 FR 21238) proposed rule solicited public
comment on each of the aforementioned issues for the following sections
of the rule that contained information collection requirements
beginning in CY 2024 through CY 2027. A summary of these comments and
our responses is in section VII.C of this final rule. The remaining
provisions are not associated with any information collection
requirements. In that regard they are not subject to the requirements
of the PRA and are not addressed under this section of the preamble.
For this rule's full burden implications, please see the Regulatory
Impact Analysis under section VIII of this final rule.
A. Wage Estimates
To derive average costs for this FY 2024 IPF PPS final rule, we
used data from the U.S. Bureau of Labor Statistics' (BLS') May 2021
National Occupational Employment and Wage Estimates for all salary
estimates (https://www.bls.gov/oes/2021/may/oes292072.htm). In this
regard, Table 25 presents BLS' median hourly wage for Medical Records
Specialists \255\ (the occupation title that we have estimated is
appropriate for completing data collection and reporting under the
IPFQR Program), our estimated cost of fringe benefits and other
indirect costs (calculated at 100 percent of salary), and our adjusted
hourly wage.
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\255\ We have previously estimated that labor performed could be
accomplished by Medical Records and Health Information Technician
staff and note that this BLS occupation category has been replaced
with Medical Records Specialists.
[GRAPHIC] [TIFF OMITTED] TR02AU23.029
As indicated, we are adjusting our hourly wage estimates by a
factor of 100 percent. This is necessarily a rough adjustment, both
because fringe benefits and other indirect costs vary significantly
from employer to employer, and because methods of estimating these
costs vary widely from study to study. Nonetheless, we believe that
doubling the hourly wage to estimate the total cost is a reasonably
accurate estimation method.
In the FY 2022 IPF PPS final rule (86 FR 42662), which was the most
recent rule in which we adopted updates to the IPFQR Program, we
estimated that reporting measures for the IPFQR Program could be
accomplished by a Medical Records and Health Information Technician
(BLS Occupation Code: 29-2072) with a median hourly wage of $20.50/hour
(BLS, May 2019). We note that since the publication of the FY 2022 IPF
PPS final rule, the BLS occupation category of `Medical Records and
Health Information Technician (BLS Occupation Code: 29-2071)' has been
replaced with `Medical Records Specialist (BLS Occupation Code: 29-
2072). Therefore, in the FY 2024 IPF PPS proposed rule, we proposed to
adjust our cost estimates using BLS' May 2021 median wage rate figure
of $22.43/hour, an increase of $1.93/hour ($22.43/hour-$20.50/hour).
When factoring in our overhead and other indirect cost adjustments, the
wage is increased by $3.86/hour ($44.86/hour-$41.00/hour).
We have also estimated the average hourly cost for patients
undertaking administrative and other tasks on their own time. Based on
recommendations from the Valuing Time in U.S. Department of Health and
Human Services Regulatory Impact Analyses \256\ guidance we have
estimated a post-tax wage of $20.71/hr. The Valuing Time in U.S.
Department of Health and Human Services Regulatory Impact Analyses:
Conceptual Framework and Best Practices identifies the approach for
valuing time when individuals undertake activities on their own time.
To derive the costs for patients, a measurement of the usual weekly
earnings of wage and salary workers of $998, divided by 40 hours to
calculate an hourly pre-tax wage rate of $24.95/hour. This rate is
adjusted downwards by an estimate of the effective tax rate for median
income households of about 17 percent, resulting in the post-tax hourly
wage rate of $20.71/hour. Unlike our State and private sector wage
adjustments, we are not adjusting beneficiary wages for fringe benefits
and other indirect costs since the individuals' activities, if any,
will occur outside the scope of their employment.
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\256\ https://aspe.hhs.gov/sites/default/files/private/pdf/257746/VOT.pdf.
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[[Page 51146]]
B. Information Collection Requirements (ICRs) Regarding the IPFQR
Program
The following changes will be submitted to OMB for approval under
control number 0938-1171 (CMS-10432). We are not making changes to any
of the data collection instruments that are currently approved under
that control number. We are, however, adopting one new instrument, the
Psychiatric Inpatient Experience survey, to calculate the patient
experience of care measure described in section VI.D.5 of this final
rule.
In section VII.B.1 of this final rule, we restate our currently
approved burden estimates. In section VII.B.2 of this final rule, we
estimate the changes in burden associated with the policies finalized
in this rule and updated estimates for wage rates, facility counts, and
case counts. Then in section VII.B.3 of this final rule, we provide an
overview of the total estimated burden.
1. Currently Approved Burden
For a detailed discussion of the burden for the IPFQR Program
requirements that we have previously adopted, we refer readers to the
FY 2022 IPF PPS final rule (86 FR 42661 through 42672).
Table 26 provides an overview of our currently approved burden
estimates.
[[Page 51147]]
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[[Page 51148]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.031
2. Adjustments Due to Changes in This Final Rule
We are finalizing provisions that impact policies beginning with
the FY 2025 through FY 2028 payment determinations. For the purposes of
calculating burden, we attribute the costs to the year in which the
costs begin. For example, data submission for the measures that affect
the FY 2025 payment determination occurs during CY 2024 and generally
reflects care provided during CY 2023. The following discussion
describes the burden changes for policies attributed to the year in
which the costs begin. For the policies in this final rule, those years
are CY 2024 through CY 2027.
Additionally, in the FY 2022 IPF PPS final rule (86 FR 42661
through 42672), which is the most recent rule that updated the IPFQR
Program policies, we estimated that there were 1,634 participating IPFs
and that (for measures that require reporting on the entire patient
population) these IPFs will report on an average of 1,346 cases per
IPF. In this FY 2024 IPF PPS final rule, we are adjusting our IPF count
and case estimates by using the most recent data available.
Specifically, we estimate that there are now approximately 1,596
facilities (a decrease of 38 facilities) and an average of 1,261 cases
per facility (a decrease of 85 cases per facility). We will update our
estimates, as applicable, using these revised estimates in the
following subsections.
a. Policies Affecting Data Reporting Beginning in CY 2023
In section VI.E. of this final rule, we are modifying the COVID-19
Vaccination Coverage Among Healthcare Personnel (HCP) measure beginning
with data reflecting the fourth quarter of CY 2023 affecting the FY
2025 payment determination. We do not believe that this modification
(that is, a change in terminology to refer to ``up-to-date'' instead of
``complete vaccination course'') will impact our currently approved IPF
information collection requirements or burden estimates because the
modified measure will be calculated using data already being submitted
by IPFs to the CDC for healthcare safety surveillance under the CDC's
OMB control number 0920-1317. In this regard, the CDC owns the
requirements and burden that fall under that control number, including
those of the COVID-19 Vaccination Coverage Among HCP measure.
b. Policies Affecting Burden Beginning With CY 2024
(1) Updates Affecting Facility Reporting Burden
In section VI.F.2 of this final rule, we are removing two measures
beginning with the FY 2025 payment determination. Data for these
measures would have been submitted in CY 2024, so we are estimating the
reduced burden to occur in CY 2024. The two measures are:
Patients Discharged on Multiple Antipsychotic Medications
with Appropriate Justification (HBIPS-5); and
Tobacco Use Treatment Provided or Offered and Tobacco Use
Treatment (TOB-2 and TOB-2a).
Using our currently approved burden estimates as a baseline, the
changes associated with removing these measures are: a decrease of
1,990,212 responses, a decrease of 497,553 hours, and a decrease of
$20,339,673 as set forth in Table 27.
[[Page 51149]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.032
Additionally, we are applying our updated wage rate (from $41.00/
hour to $44.86/hour), case count (from 1,346 to 1,261), and facility
counts (from 1,634 to 1,596) to the remaining measure set and program
requirements for data submission in CY 2024. See Table 28 and 29 for
information on the effects of these updates. Specifically, we estimate
that there are now approximately 1,596 facilities (a decrease of 38
facilities) and an average of 1,261 cases per facility (a decrease of
85 cases per facility). We also estimate a wage increase of $3.86/hour
as described in section VI.A of this final rule. Our previous estimate
shows that the two measures which do not allow sampling had 1,346 cases
per measure and the six remaining measures which do allow sampling
require 609 cases per measure per facility. We have estimated that
these measures will take 0.25 hours per case. The effects of the
updated hourly wage are set forth in Table 28.
[GRAPHIC] [TIFF OMITTED] TR02AU23.033
The remaining calculations will use the updated hourly wage to
calculate the effects of other updates.
Our active burden estimates account for 1,346 cases for measures
that do not allow sampling. Based on more recent data, we are updating
our estimate for measures that do not allow sampling to 1,261 cases per
IPF (a decrease of 85
[[Page 51150]]
cases for each of the 2 measures which do not allow sampling). This is
equivalent to 138,890 cases across the 1,634 IPFs (85 cases x 1,634
IPFs) in our previous estimate for each measure. We are not changing
our estimated case counts for measures that allow sampling. We continue
to assume an average of 0.25 hours of effort per case. Therefore, this
change in cases reflects a total annual effort of 42.5 hours per
facility (2 measures * 85 cases per measure * 0.25 hours per case) at a
cost of $1,907 (42.5 hours * $44.86/hour).
As indicated above we estimate a reduction of 38 facilities based
on updated numbers. Table 29 shows the effects of this reduction in
facilities on the reporting burden associated with each measure type.
[GRAPHIC] [TIFF OMITTED] TR02AU23.034
We note that at 6,180 cases per facility, removing 38 facilities
from our estimate removes a total of 234,840 cases (6,180 cases per
facility * 38 facilities).
The total effects of changes for the CY 2024 calendar year on our
burden estimates are summarized in Table 30.
[GRAPHIC] [TIFF OMITTED] TR02AU23.035
(2) Updates Affecting Patient Survey Burden
In section VI.D.3 of this final rule, we are adopting the Screening
for Social Drivers of Health measure beginning with a voluntary data
submission in CY 2025 (reflecting care provided in CY 2024). IPFs will
be able to collect data and report the measure via multiple methods,
potentially including administrative claims data, electronic clinical
data, standardized patient assessments, or patient-reported data and
surveys. For additional information on these methods, we refer readers
to section VI.D.3.c of this final rule. We believe that most IPFs will
likely collect data during the patient intake process. Because this
measure reflects care provided in CY 2024, the burden for administering
the screening to patients will occur during CY 2024.
Under OMB Control Number 0938-1022 (CMS-10210) and the FY 2022
IPPS/LTCH PPS final rule (87 FR 49385 through 49386), the Hospital IQR
Program, which adopted the Screening for Social Drivers of Health
measure, estimates that it will take 2 minutes (0.033 hr) per patient
to complete the selected screening instrument. The Hospital IQR Program
also estimated that during the voluntary reporting period roughly 50
percent of hospitals will survey 50 percent of patients (87 FR 49385
through 49386).
We agree with these estimates and believe that a similar proportion
of IPFs will participate in the voluntary reporting period. As
described in section VII.A of this final rule, we estimate the cost of
patients' time for completing surveys to be $20.71/hour. Using these
estimates, we believe that during the voluntary reporting period the
annual burden of surveying IPF patients will be 503,139 responses
[(1,596 facilities x 50 percent of facilities) x (1,261 patients per
facility x 50 percent of patients)], 16,604 hours (503,139 responses x
0.033 hours/response] at a cost of $343,869 (16,604 hours x $20.71/
hour). These estimates are summarized in Table 31.
[[Page 51151]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.036
c. Policies Affecting Burden Beginning With CY 2025
(1) Updates Affecting Facility Reporting Burden
In section VI.I.5 of this final rule, we are adopting a data
validation pilot for the IPFQR Program. Under this pilot we will
reimburse hospitals directly for expenses associated with submission of
charts for clinical process of care measure data validation. Because we
will reimburse facilities directly for these expenses we do not believe
that this pilot will increase information collection burden.
In section VI.D.2. of this final rule, we are adopting the Facility
Commitment to Health Equity measure beginning with the FY 2026 payment
determination. Data for this attestation measure will be submitted
during CY 2025. Consistent with our burden estimate from the Hospital
IQR Program, when we adopted the similar Hospital Commitment to Health
Equity measure in the FY 2023 IPPS/LTCH PPS final rule, we estimated an
average of 10 minutes per facility for a medical records specialist to
collect and report this information (87 FR 49385). We recognize that
some IPFs may take more than 10 minutes to collect this information,
especially in the first year of reporting; however, we believe that
many IPFs will require less than 10 minutes. In addition, we believe
that many IPFs will be able to submit similar responses in future
years. Using the estimate of 10 minutes (0.167 hour) per IPF per year
at $44.86/hour for a medical records specialist, we estimate that this
policy will result in a total annual burden increase of 267 hours
(0.167 hours x 1,596 IPFs) at a cost of $11,956.63 (267 hours x $44.86/
hour) across all participating IPFs.
In sections VI.D.3 and VI.D.4 of this final rule, we are adopting
the Screening for Social Drivers of Health measure and the associated
Screen Positive Rate for Social Drivers of Health measure beginning
with a voluntary data submission in CY 2025 (reflecting care provided
in CY 2024). We described our anticipated burden (16,604 hours at a
cost of $343,869) for administering the screening in the previous
section because this burden will accrue during CY 2024. The burden
associated with reporting each of these measures to CMS will occur
during CY 2025. We anticipate that the burden for reporting the two
measures will be consistent with the burden for other web-based
submissions, such as the Facility Commitment to Health Equity measure
described previously in this section and for similar measures adopted
in the Ambulatory Surgical Center Quality Reporting (ASCQR) Program
(OMB control number 0938-1270; CMS-10530), which we have estimated to
have a reporting burden of 10 minutes (0.167 hours) per facility. We
note that for the voluntary reporting year we have estimated only 50
percent or 798 IPFs (1,596 IPFs x 0.50) will report these data.
Therefore, we estimate the burden associated with reporting of each of
these measures to be 133 hours (0.167 hr. x 798 IPFs) at a cost of
$5,966 (133 hr. x $44.86/hour) for a medical records specialist) for
the voluntary reporting period. These estimates are summarized in Table
32.
[GRAPHIC] [TIFF OMITTED] TR02AU23.037
[[Page 51152]]
(2) Updates Affecting Patient Survey Burden
Beginning with CY 2025, IPFs will need to screen 100 percent of
their patients to prepare for mandatory reporting of the Screening for
Social Drivers of Health measure in CY 2026 (for the FY 2027 payment
determination). Therefore, we estimate that 100 percent of IPFs will
screen 100 percent of their patients. We recognize that this may be an
overestimate as some IPFs may choose not to participate and some
patients may opt out of screening or be unable to provide responses;
however, we believe that the numbers of IPFs and patients opting out
will be relatively small and therefore 100 percent will be a reasonable
approximation.
Using the facility counts (1,596 facilities), patient counts (1,261
patients per facility), average hourly earnings ($20.71/hour), and time
per response (10 min or 0.033 hours) described previously, we estimate
the burden of surveying IPF patients for health-related social needs
(HRSNs) under the Screening for Social Drivers of Health and Screen
Positive Rate for Social Drivers of Health measures will be 66,414
hours (1,596 facilities x 1,261 patients per facility x 0.033 hr) at a
cost of $1,375,434 (66,414 hour x $20.71/hour) across all patients. We
note that 16,604 hours and $343,960 of this burden was accounted for in
our analysis of the burden of the voluntary reporting period described
in section VII.B.2.c.(2). Therefore, the incremental burden of
switching to mandatory reporting is 49,810 hours (66,414 hours-16,604
hours) and $1,031,474 ($1,375,434-$343,960).
Additionally, in section VI.D.5 of this final rule, we are adopting
the Psychiatric Inpatient Experience (PIX) survey measure beginning
with voluntary data submission in CY 2026. To prepare for data
submission in 2026, IPFs will begin administering this survey in CY
2025. We believe 50 percent or 798 (1,596 facilities x 0.50) of IPFs
would begin collecting these data for the voluntary data submission
period. We note that we proposed to allow IPFs with more than 300
eligible discharges to sample, which would require these facilities to
survey 300 patients. Because the questions on the PIX survey are
similar in content and response options to the questions on the
Hospital Consumer Assessment of Healthcare Providers and Systems
(HCAHPS) survey, we believe that it will take patients a similar amount
of time to respond to these questions. In the Information Collection
Request associated with OMB control number 0938-0981 (CMS-10102), we
have estimated this time to be 7.25 minutes (0.121 hours).
Therefore, we believe that the burden associated with conducting
the PIX survey in CY 2025 will be 28,967 hours (798 facilities x 300
patients/facility x 0.121 hours/response) at a cost of $599,907 (28,967
hours x $20.71/hour).
Our estimates for the CY 2025 total patient survey burden changes
are summarized in Table 33.
[GRAPHIC] [TIFF OMITTED] TR02AU23.038
d. Policies Affecting Burden Beginning With CY 2026
(1) Updates Affecting Facility Reporting Burden
Beginning with CY 2026 data submission (affecting the FY 2027
payment determination), we estimate that 100 percent of IPFs will
submit data on the Screening for Social Drivers of Health measure and
Screen Positive Rate for Social Drivers of Health measure. Because we
have already accounted for 50 percent of facilities submitting
voluntary data on these measures, the incremental burden is the burden
associated with the remaining 50 percent of facilities submitting data;
that is, we estimate this burden to be 266 hours at a cost of $11,933.
We also believe that 50 percent of facilities will submit data on the
PIX survey measure for the voluntary reporting period in CY 2025.
Because the data for this measure will require calculating an average
of scores across a sample of patient surveys, we anticipate that the
information collection and reporting burden for this measure will be
approximately 15 minutes (0.25 hours) per patient for whom they are
reporting data. The burden associated with reporting the Screening for
Social Drivers of Health measure, the Screen Positive Rate for Social
Drivers of Health measure, and the PIX survey measure to CMS is
described in Table 34.
[[Page 51153]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.039
(2) Updates Affecting Patient Survey Burden
Because reporting the PIX survey measure will be mandatory for the
FY 2028 payment determination, the remaining 50 percent of facilities
(those which did not participate in the voluntary reporting period)
will begin surveying patients in CY 2026. To prepare for data
submission of the PIX survey measure to CMS in CY 2027, IPFs that had
not previously begun administering the PIX survey will begin
administering this survey in CY 2026. The incremental burden of these
50 percent of facilities administering the survey will be equivalent to
the burden associated with the 50 percent of facilities that
participated in the voluntary reporting in CY 2025. These estimates are
summarized in Table 35.
[GRAPHIC] [TIFF OMITTED] TR02AU23.040
e. Policies Affecting Facility Reporting Burden Beginning With CY 2027
For data submission occurring in CY 2027, submission on the PIX
survey measure will be mandatory, therefore, we believe that an
additional 50 percent of facilities will report the measure (that is,
the 50 percent of facilities not previously accounted for under the
voluntary reporting period). Therefore, we estimate that the
incremental increase in burden for IPFs associated with this
requirement will be reporting by the 50 percent of facilities that had
not previously reported the PIX survey measure. This burden is set
forth in Table 36.
[GRAPHIC] [TIFF OMITTED] TR02AU23.041
[[Page 51154]]
3. Overall Burden Summary
Table 37 summarizes the incremental changes in burden for IPFs
associated with policies for data collection and submission in CYs 2024
through 2027 as well as updates to our estimated wage rate, facility
counts, and case counts.
[GRAPHIC] [TIFF OMITTED] TR02AU23.042
Table 38 summarizes the incremental changes in burden for patients
due to data collection associated with proposed policies for data
collection and submission in CYs 2024 through CY 2026.
[GRAPHIC] [TIFF OMITTED] TR02AU23.043
Table 39 summarizes the total annual change in burden associated
with the IPFQR Program's finalized policies in this final rule. These
figures are calculated by adding the annual changes in Table 37 with
the annual changes in Table 38. We note that these figures represent
the changes to our previously approved burden (set forth in Table 26 of
this final rule).
[[Page 51155]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.044
C. Comments Received on the Proposed Collection of Information
Requirements
We solicited public comment on our estimated burden associated with
the information collection requirements.
The following comments were received.
Comment: Several commenters expressed concern that the policies
under the IPFQR Program will be burdensome, and some commenters
specifically noted burden related to the PIX survey. One commenter
expressed the belief that removing two measures while adopting four
measures would increase overall burden.
Response: We understand commenters' concerns that some of the
policies under the IPFQR Program may contribute to IPF reporting
burden. With respect to the PIX survey, we do not believe that
administering a patient experience of care survey will be unduly
burdensome for the majority of IPFs that previously self-reported that
they already administer such a survey when responding to the IPFQR
Program's former Assessment of Patient Experience of Care measure. We
recognize that there will be some non-recurring burden for these IPFs
to transition to the newly adopted survey. With respect to the concern
that removing two measures while adopting four measures would increase
the overall burden, we note that the measures we are removing are
chart-abstracted measures with high reporting burden. We estimate that
the newly adopted measures require less time to calculate and report.
Therefore, we believe that our estimate that the overall burden of the
IPFQR Program will be decreased by these policies is accurate.
VIII. Regulatory Impact Analysis
A. Statement of Need
This rule finalizes updates to the prospective payment rates for
Medicare inpatient hospital services provided by IPFs for discharges
occurring during FY 2024 (October 1, 2023 through September 30, 2024).
We are finalizing our proposal to apply a 2021-based IPF market basket
increase for FY 2024 of 3.5 percent, less the productivity adjustment
of 0.2 percentage point as required by 1886(s)(2)(A)(i) of the Act for
a final total FY 2024 payment rate update of 3.3 percent. In this final
rule, we are finalizing our proposal to update the outlier fixed dollar
loss threshold amount, update the IPF labor-related share, and update
the IPF wage index to reflect the FY 2024 hospital inpatient wage
index. Section 1886(s)(3)(4) of the Act requires IPFs to report data in
accordance with the requirements of the IPFQR Program for purposes of
measuring and making publicly available information on health care
quality, and links the quality data submission to the annual applicable
percentage increase.
B. Overall Impact
We have examined the impacts of this rule as required by Executive
Order 12866 on Regulatory Planning and Review (September 30, 1993),
Executive Order 13563 on Improving Regulation and Regulatory Review
(January 18, 2011), Executive Order 14094 entitled ``Modernizing
Regulatory Review'' (April 6, 2023), the Regulatory Flexibility Act
(RFA) (September 19, 1980, Pub. L. 96-354), section 1102(b) of the
Social Security Act, section 202 of the Unfunded Mandates Reform Act of
1995 (March 22, 1995; Pub. L. 104-4), Executive Order 13132 on
Federalism (August 4, 1999), and the Congressional Review Act (5 U.S.C.
804(2)).
Executive Orders 12866 and 13563 direct agencies to assess all
costs and benefits of available regulatory alternatives and, if
regulation is necessary, to select regulatory approaches that maximize
net benefits (including potential economic, environmental, public
health and safety effects, distributive impacts, and equity). The
Executive Order 14094 entitled ``Modernizing Regulatory Review''
(hereinafter, the Modernizing E.O.) amends section 3(f)(1) of Executive
Order 12866 (Regulatory Planning and Review). The amended section 3(f)
of Executive Order 12866 defines a ``significant regulatory action'' as
an action that is likely to result in a rule: (1) having an annual
effect on the economy of $200 million or more in any 1 year (adjusted
every 3 years by the Administrator of OIRA for changes in gross
domestic product), or adversely affect in a material way the economy, a
sector of the economy, productivity, competition, jobs, the
environment, public health or safety, or State, local,
[[Page 51156]]
territorial, or tribal governments or communities; (2) creating a
serious inconsistency or otherwise interfering with an action taken or
planned by another agency; (3) materially altering the budgetary
impacts of entitlement grants, user fees, or loan programs or the
rights and obligations of recipients thereof; or (4) raising legal or
policy issues for which centralized review would meaningfully further
the President's priorities or the principles set forth in the order, as
specifically authorized in a timely manner by the Administrator of OIRA
in each case.
A regulatory impact analysis (RIA) must be prepared for major rules
with significant regulatory action(s) and/or with significant effects
as per section 3(f)(1) ($200 million or more in any 1 year). We
estimate that the total impact of these changes for FY 2024 payments
compared to FY 2023 payments will be a net increase of approximately
$70 million. This reflects a $95 million increase from the update to
the payment rates (+$100 million due to the FY 2024IPF market basket
update of 3.5 percent, and -$5 million for the productivity adjustment
of 0.2 percentage point), as well as a $25 million decrease as a result
of the update to the outlier threshold amount. Outlier payments are
estimated to change from 2.9 percent in FY 2023 to 2.0 percent of total
estimated IPF payments in FY 2024.
Based on our estimates, OMB's Office of Information and Regulatory
Affairs has determined that this rulemaking is not significant per
section 3(f)(1) as measured by the $200 million threshold or more in
any 1 year. Nevertheless, this rule is a major rule, and accordingly,
we have prepared a Regulatory Impact Analysis that to the best of our
ability presents the costs and benefits of the rulemaking. Therefore,
OMB has reviewed this final regulation, and we have provided the
following assessment of its impact.
C. Detailed Economic Analysis
In this section, we discuss the historical background of the IPF
PPS and the impact of this final rule on the Federal Medicare budget
and on IPFs.
1. Budgetary Impact
As discussed in the November 2004 and RY 2007 IPF PPS final rules,
we applied a budget neutrality factor to the Federal per diem base rate
and ECT payment per treatment to ensure that total estimated payments
under the IPF PPS in the implementation period will equal the amount
that would have been paid if the IPF PPS had not been implemented. This
Budget neutrality factor included the following components: Outlier
adjustment, stop loss adjustment, and the behavioral offset. As
discussed in the RY 2009 IPF PPS notice (73 FR 25711), the stop-loss
adjustment is no longer applicable under the IPF PPS.
As discussed in section III.D.1 of this final rule, we proposed to
update the wage index and labor-related share in a budget neutral
manner by applying a wage index budget neutrality factor to the Federal
per diem base rate and ECT payment per treatment. Therefore, the
budgetary impact to the Medicare program of this final rule will be due
to the IPF market basket update for FY 2024 of 3.5 percent (see section
IV.A.2 of this final rule) reduced by the productivity adjustment of
0.2 percentage point as required by section 1886(s)(2)(A)(i) of the Act
and the update to the outlier fixed dollar loss threshold amount.
We estimate that the FY 2024 impact will be a net increase of $70
million in payments to IPF providers. This reflects an estimated $95
million increase from the update to the payment rates and a $25 million
decrease due to the update to the outlier threshold amount to set total
estimated outlier payments at 2.0 percent of total estimated payments
in FY 2024. This estimate does not include the implementation of the
mandatory 2.0 percentage point reduction of the productivity-adjusted
IPF market basket update factor for any IPF that fails to meet the IPF
quality reporting requirements (as discussed in section IV.B.2. of this
final rule).
2. Impact on Providers
To show the impact on providers of the changes to the IPF PPS
discussed in this final rule, we compare estimated payments under the
proposed IPF PPS rates and factors for FY 2024 versus those under FY
2023. We determined the percent change in the estimated FY 2024 IPF PPS
payments compared to the estimated FY 2023 IPF PPS payments for each
category of IPFs. In addition, for each category of IPFs, we have
included the estimated percent change in payments resulting from the
final update to the outlier fixed dollar loss threshold amount; the
updated wage index data including the final labor-related share; and
the final IPF market basket update for FY 2024, as reduced by the final
productivity adjustment according to section 1886(s)(2)(A)(i) of the
Act.
To illustrate the impacts of the FY 2024 changes in this final
rule, our analysis begins with FY 2022 IPF PPS claims (based on the
2022 MedPAR claims, March 2023 update). We estimate FY 2023 IPF PPS
payments using these 2022 claims, the finalized FY 2023 IPF PPS Federal
per diem base rates, and the finalized FY 2023 IPF PPS patient and
facility level adjustment factors (as published in the FY 2023 IPF PPS
final rule (87 FR 46846)). We then estimate the FY 2024 outlier
payments based on these simulated FY 2023 IPF PPS payments using the
same methodology that we used to set the initial outlier threshold
amount in the RY 2007 IPF PPS final rule (71 FR 27072 and 27073), which
is also the same methodology that we used to update the outlier
threshold amounts for years 2008 through 2022, where total outlier
payments are maintained at 2 percent of total estimated FY 2023 IPF PPS
payments. We note that in the FY 2023 final rule (87 FR 46862 through
46864) we excluded providers from our simulation of IPF PPS payments
for FY 2022 and FY 2023 if their change in estimated average cost per
day was outside 3 standard deviations from the mean. As discussed in
section IV.E.2 of this final rule, we did not propose to apply this
methodology for FY 2024.
Each of the following changes is added incrementally to this
baseline model in order for us to isolate the effects of each change:
The update to the outlier fixed dollar loss threshold
amount.
The FY 2024 IPF wage index and the FY 2024 labor-related
share.
The IPF market basket update for FY 2024 of 3.5 percent
less the productivity adjustment of 0.2 percentage point in accordance
with section 1886(s)(2)(A)(i) of the Act for a final IPF payment rate
update of 3.3 percent.
Our column comparison in Table 40 illustrates the percent change in
payments from FY 2023 (that is, October 1, 2022, to September 30, 2023)
to FY 2024 (that is, October 1, 2023, to September 30, 2024) including
all the payment policy changes.
[[Page 51157]]
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[[Page 51158]]
[GRAPHIC] [TIFF OMITTED] TR02AU23.046
3. Impact Results
Table 40 displays the results of our analysis. The table groups
IPFs into the categories listed here based on characteristics provided
in the Provider of Services file, the IPF PSF, and cost report data
from the Healthcare Cost Report Information System:
Facility Type.
Location.
Teaching Status Adjustment.
Census Region.
Size.
The top row of the table shows the overall impact on the 1,479 IPFs
included in the analysis. In column 2, we present the number of
facilities of each type that had information available in the PSF and
had claims in the MedPAR dataset for FY 2022.
In column 3, we present the effects of the update to the outlier
fixed dollar loss threshold amount. We estimate that IPF outlier
payments as a percentage of total IPF payments are 2.9 percent in FY
2023. Therefore, we adjusted the outlier threshold amount to set total
estimated outlier payments equal to 2.0 percent of total payments in FY
2024. The estimated change in total IPF payments for FY 2024,
therefore, includes an approximate 0.9 percent decrease in payments
because we expect the outlier portion of total payments to decrease
from approximately 2.9 percent to 2.0 percent.
The overall impact of the estimated decrease to payments due to
updating the outlier fixed dollar loss threshold (as shown in column 3
of Table 3), across all hospital groups, is a 0.9 percentage point
decrease. The largest decrease in payments due to this change is
estimated to be 2.6 percent for urban government unit IPFs.
In column 4, we present the effects of the budget-neutral update to
the IPF wage index, the Labor-Related Share (LRS), and the 5-percent
cap on any decrease to a provider's wage index from its wage index in
the prior year. This represents the effect of using the concurrent
hospital wage data as discussed in section IV.D.1.a of this final rule.
That is, the impact represented in this column reflects the update from
the FY 2023 IPF wage index to the FY 2024 IPF wage index, which
includes basing the FY 2024 IPF wage index on the FY 2024 pre-floor,
pre-reclassified IPPS hospital wage index data, applying a 5-percent
cap on any decrease to a provider's wage index from its wage index in
the prior year, and updating the LRS from 77.4 percent in FY 2023 to
78.7 percent in FY 2024. We note that there is no projected change in
aggregate payments to IPFs, as indicated in the first row of column 4;
however, there will be distributional effects among different
categories of IPFs. For example, we estimate the largest increase in
payments to be 1.1 percent for Mid-Atlantic IPFs, and the largest
decrease in payments to be 1.3 percent for freestanding, rural, for-
profit IPFs.
Column 5 incorporates the FY 2024 IPF market basket update of 3.5
percent reduced by 0.2 percentage point for the productivity adjustment
as required by section 1886(s)(2)(A)(i) of the Act. This includes
rebasing the IPF market basket to reflect a 2021 base year.
Overall, IPFs are estimated to experience a net increase in
payments as a result of the updates in this final rule. IPF payments
are estimated to increase by 2.4 percent in urban areas and 2.0 percent
in rural areas. The largest payment increases are estimated at 3.4
percent for freestanding, urban, non-profit IPFs.
4. Effect on Beneficiaries
Under the FY 2024 IPF PPS, IPFs will continue to receive payment
based on the average resources consumed by patients for each day. Our
longstanding payment methodology reflects the differences in patient
resource use and costs among IPFs, as required under section 124 of the
BBRA. We expect that updating IPF PPS rates in this final rule will
improve or maintain beneficiary access to high quality care by ensuring
that payment rates reflect the best available data on the resources
involved in inpatient psychiatric care and the
[[Page 51159]]
costs of these resources. We continue to expect that paying
prospectively for IPF services under the FY 2024 IPF PPS will enhance
the efficiency of the Medicare program.
As discussed in sections VI.D.3 and VI.D.4 of this final rule, we
expect that additional IPFQR Program measures will support improving
care for patients with health-related social needs. We also believe
that our data validation pilot is an important step towards ensuring
that the data beneficiaries and their caregivers access on Care Compare
(or a successor CMS website) are accurate and reliable. Based on the
input from patients and their caregivers regarding the importance of
having a patient experience of care measure for the IPF setting in
which they note many benefits (including, but not limited to helping
patients select facilities in which to receive care, providing patients
an opportunity to be heard, and increasing alignment between general
acute and acute psychiatric settings). We believe that our PIX survey
measure will have positive effects on patients and their caregivers.
Therefore, we expect that the updates to the IPFQR Program will improve
quality for beneficiaries.
5. Effects of the Updates to the IPFQR Program
In section VI.D.3 of this final rule, we are adopting the Screening
for Social Drivers of Health measure for the IPFQR Program beginning
with voluntary reporting of CY 2024 data, and with mandatory reporting
of CY 2025 data for the FY 2027 payment determination. For IPFs that
are not currently administering some screening mechanism and elect to
begin doing so as a result of this policy, there will be some non-
recurring costs associated with changes in workflow and information
systems to collect the data. The extent of these costs is difficult to
quantify as different facilities may utilize different modes of data
collection (for example, paper-based, electronically patient-directed
and clinician-facilitated). In addition, depending on the method of
data collection utilized, the time mandatory to complete the survey may
add a negligible amount of time to patient visits.
In section VI.D.5 of this final rule, we are adopting the
Psychiatric Inpatient Experience (PIX) survey measure. There may be
some non-recurring costs associated with changes in workflow and
information systems to administer this survey and collect the data. The
extent of these costs is difficult to quantify as different facilities
currently have different practices for surveying patients to gather
information on their experiences of care.
In addition, for the IPFQR Program, we are adopting the Facility
Commitment to Health Equity measure and the Screen Positive for Social
Drivers of Health measure, as well as to update the COVID-19
Vaccination Coverage Among HCP measure. These updates will not impact
providers workflows or information systems to collect or report the
data, and because they represent processes of care or structural data
that the IPFs will already have in place, we do not believe they will
incur costs for providers beyond the recurring information collection
costs (described in section VII.B of this final rule).
Finally, we are removing two chart-abstracted measures from the
IPFQR Program. We believe that the impact of removing the Tobacco Use
Brief Intervention Provided or Offered and Tobacco Use Brief
Intervention Provided (TOB-2/2a) measure will be minimal as we do not
believe that IPFs will update their workflow to no longer provide brief
tobacco cessation interventions to patients who use tobacco. However,
we believe that there may be some simplification of workflows and
clinical documentation associated with the removal of the Patients
Discharged on Multiple Antipsychotic Medications with Appropriate
Justification (HBIPS-5) measure because IPFs will no longer have to
ensure the presence of appropriate documentation for the use of
multiple antipsychotics. For more information on the updated clinical
guidelines regarding polypharmacy for patients with schizophrenia, we
refer readers to section VI.F.2.a of this final rule.
As discussed in section IV.B.2 of this final rule and in accordance
with section 1886(s)(4)(A)(i) of the Act, we will apply a 2-percentage
point reduction to the FY 2024 market basket update for IPFs that have
failed to comply with the IPFQR Program requirements for FY 2024,
including reporting on the mandatory measures. In section IV.B.2 of
this final rule, we discuss how the 2-percentage point reduction will
be applied. For the FY 2023 payment determination, of the 1,596 IPFs
eligible for the IPFQR Program, 6 IPFs did not receive the full market
basket update because of the IPFQR Program; 2 of these IPFs chose not
to participate and 4 did not meet the requirements of the program.
Thus, we estimate that the IPFQR Program will have a negligible impact
on overall IPF payments for FY 2024.
Based on the IPFQR Program policies in this final rule, we estimate
a total decrease in burden of 380,897 hours across all IPFs, resulting
in a total decrease in information collection cost of $8.15 million
across all IPFs. Further information on these estimates can be found in
section VII.B of this final rule.
We intend to closely monitor the effects of the IPFQR Program on
IPFs and help facilitate successful reporting outcomes through ongoing
stakeholder education, national trainings, and a technical help desk.
6. Regulatory Review Costs
If regulations impose administrative costs on private entities,
such as the time needed to read and interpret this final rule, we
should estimate the cost associated with regulatory review. Due to the
uncertainty involved with accurately quantifying the number of entities
that will be directly impacted and will review this final rule, we
assume that the total number of unique commenters on the most recent
IPF PPS proposed rule will be the number of reviewers of this final
rule. For this FY 2024 IPF PPS final rule, the most recent IPF PPS
proposed rule was the FY 2024 IPF PPS proposed rule, and we received
2,506 unique comments on this proposed rule. We acknowledge that this
assumption may understate or overstate the costs of reviewing this
final rule. It is possible that not all commenters reviewed the FY 2024
IPF PPS proposed rule in detail, and it is also possible that some
reviewers chose not to comment on that proposed rule. For these
reasons, we thought that the number of commenters will be a fair
estimate of the number of reviewers who are directly impacted by this
final rule. We solicited comments on this assumption.
We also recognize that different types of entities are in many
cases affected by mutually exclusive sections of this final rule;
therefore, for the purposes of our estimate, we assume that each
reviewer reads approximately 50 percent of this final rule. Using the
May, 2022 mean (average) wage information from the BLS for medical and
health service managers (Code 11-9111), we estimate that the cost of
reviewing this final rule is $123.06 per hour, including overhead and
fringe benefits https://www.bls.gov/oes/current/oes119111.htm. Assuming
an average reading speed of 250 words per minute, we estimate that it
will take approximately 198 minutes (3.3 hours) for the staff to review
half of this final rule (49,500), which contains a total of
approximately 99,000 words. For each IPF that reviews the final rule,
the estimated cost is (3.3 x $123.06) or
[[Page 51160]]
$406.10. Therefore, we estimate that the total cost of reviewing this
final rule is $1,017,686.60 ($406.10 x 2,506 reviewers).
D. Alternatives Considered
The statute does not specify an update strategy for the IPF PPS and
is broadly written to give the Secretary discretion in establishing an
update methodology. We continue to believe it is appropriate to
routinely update the IPF PPS so that it reflects the best available
data about differences in patient resource use and costs among IPFs as
required by the statute. Therefore, we are finalizing our proposal to:
Update the IPF PPS using the methodology published in the November 2004
IPF PPS final rule; apply the 2021-based IPF market basket update for
FY 2024 of 3.5 percent reduced by the productivity adjustment of 0.2
percentage point as required by section 1886(s)(2)(A)(i) of the Act
along with the wage index budget neutrality adjustment to update the
payment rates; and use a FY 2024 IPF wage index which uses the FY 2024
pre-floor, pre-reclassified IPPS hospital wage index as its basis.
Lastly, we solicited comments on alternative methodologies that
could be appropriate for establishing the FY 2024 outlier fixed dollar
loss threshold.
E. Accounting Statement
As required by OMB Circular A-4 (https://www.whitehouse.gov/wp-content/uploads/legacy_drupal_files/omb/circulars/A4/a-4.pdf), in Table
41, we have prepared an accounting statement showing the classification
of the expenditures associated with the updates to the IPF wage index
and payment rates in this final rule. Table 41 provides our best
estimate of the increase in Medicare payments under the IPF PPS as a
result of the changes presented in this final rule and is based on
1,479 IPFs with data available in the PSF and with claims in our FY
2022 MedPAR claims dataset. Lastly, Table 41 also includes our best
estimate of the costs of reviewing and understanding this final rule.
[GRAPHIC] [TIFF OMITTED] TR02AU23.047
F. Regulatory Flexibility Act
The RFA requires agencies to analyze options for regulatory relief
of small entities if a rule has a significant impact on a substantial
number of small entities. For purposes of the RFA, small entities
include small businesses, nonprofit organizations, and small
governmental jurisdictions. Most IPFs and most other providers and
suppliers are small entities, either by nonprofit status or having
revenues of $8 million to $41.5 million or less in any 1 year.
Individuals and states are not included in the definition of a small
entity.
Because we lack data on individual hospital receipts, we cannot
determine the number of small proprietary IPFs or the proportion of
IPFs' revenue derived from Medicare payments. Therefore, we assume that
all IPFs are considered small entities.
The Department of Health and Human Services generally uses a
revenue impact of 3 to 5 percent as a significance threshold under the
RFA. As shown in Table 40, we estimate that the overall revenue impact
of this final rule on all IPFs is to increase estimated Medicare
payments by 2.3 percent. As a result, since the estimated impact of
this final rule is a net increase in revenue across almost all
categories of IPFs, the Secretary has determined that this final rule
will have a positive revenue impact on a substantial number of small
entities.
In addition, section 1102(b) of the Act requires us to prepare a
regulatory impact analysis if a rule may have a significant impact on
the operations of a substantial number of small rural hospitals. This
analysis must conform to the provisions of section 604 of the RFA. For
purposes of section 1102(b) of the Act, we define a small rural
hospital as a hospital that is located outside of a metropolitan
statistical area and has fewer than 100 beds. As discussed in section
VIII.C.2 of this final rule, the rates and policies set forth in this
final rule will not have an adverse impact on the rural hospitals based
on the data of the 211 rural excluded psychiatric units and 61 rural
psychiatric hospitals in our database of 1,479 IPFs for which data were
available. Therefore, the Secretary has determined that this final rule
will not have a significant impact on the operations of a substantial
number of small rural hospitals.
G. Unfunded Mandate Reform Act (UMRA)
Section 202 of the Unfunded Mandates Reform Act of 1995 (UMRA) also
requires that agencies assess anticipated costs and benefits before
issuing any rule whose mandates require spending in any 1 year of $100
million in 1995 dollars, updated annually for inflation. In 2023, that
threshold is approximately $177 million. This final rule does not
mandate any requirements for state, local, or tribal governments, or
for the private sector. This final rule will not impose a mandate that
will result in the expenditure by state, local, and tribal governments,
in the aggregate, or by the private sector, of more than $177 million
in any 1 year.
H. Federalism
Executive Order 13132 establishes certain requirements that an
agency must meet when it promulgates a proposed rule that imposes
substantial direct requirement costs on state and local governments,
preempts state law, or otherwise has Federalism implications. This
final rule does not impose substantial direct costs on state
[[Page 51161]]
or local governments or preempt state law.
Chiquita Brooks-LaSure, Administrator of the Centers for Medicare &
Medicaid Services, approved this document on July 24, 2023.
List of Subjects in 42 CFR Part 412
Administrative practice and procedure, Health facilities, Medicare,
Puerto Rico, Reporting and recordkeeping requirements.
For the reasons set forth in the preamble, the Centers for Medicare
& Medicaid Services amends 42 CFR part 412 as set forth below:
PART 412--PROSPECTIVE PAYMENT SYSTEMS PROSPECTIVE PAYMENT SYSTEMS
FOR INPATIENT HOSPITAL SERVICES
0
1. The authority citation for part 412 continues to read as follows:
Authority: 42 U.S.C. 1302 and 1395hh.
0
2. Section 412.25 is amended by revising paragraph (c) to read as
follows:
Sec. 412.25 Excluded hospital units: Common requirements.
* * * * *
(c) The status of a hospital unit may be changed from not excluded
to excluded or excluded to not excluded at any time during a cost
reporting period, but only if the hospital notifies the fiscal
intermediary and the CMS Regional Office in writing of the change at
least 30 days before the date of the change, and maintains the
information needed to accurately determine costs that are or are not
attributable to the hospital unit. A change in the status of a hospital
unit from not excluded to excluded or excluded to not excluded that is
made during a cost reporting period must remain in effect for the rest
of that cost reporting period.
* * * * *
0
3. Section 412.433 is added to read as follows:
Sec. 412.433 Procedural requirements under the IPFQR Program.
(a) Statutory authority. Section 1886(s)(4) of the Act requires the
Secretary to implement a quality reporting program for inpatient
psychiatric hospitals and psychiatric units. Under section 1886(s)(4)
of the Act, for an IPF paid under the IPF PPS that fails to submit data
required for the quality measures selected by the Secretary in a form
and manner and at a time specified by the Secretary, we reduce the
otherwise applicable annual update to the standard Federal rate by 2.0
percentage points with respect to the applicable fiscal year.
(b) Participation in the IPFQR Program. To participate in the IPFQR
Program, an IPF (as defined under Sec. 412.402) that is paid under the
IPF PPS must:
(1) Register and maintain an account on the CMS-designated
information system before beginning to report data, identification of a
security official is necessary to complete such registration; and
(2) Submit a notice of participation (NOP).
(c) Withdrawal from the IPFQR Program. An IPF may withdraw from the
IPFQR Program by changing the NOP status in the secure portion of the
CMS-designated information system. The IPF may withdraw at any time up
to and including August 15 before the beginning of each respective
payment determination year. A withdrawn IPF is subject to a reduced
annual payment update as specified under paragraph (a) of this section
and is mandatory to renew participation as specified in paragraph (b)
of this section in order to participate in any future year of the IPFQR
Program.
(d) Submission of IPFQR Program data. In general, except as
provided in paragraph (f) of this section, IPFs that participate in the
IPFQR Program must submit to CMS data on measures selected under
section 1886(s)(4)(D) of the Act and specified non-measure data in a
form and manner, and at a time specified by CMS.
(e) Quality measure updates, retention, and removal. (1) General
rule for updates to quality measures. CMS uses rulemaking to make
substantive updates to the specifications of measures used in the IPFQR
Program
(2) General rule for the retention of quality measures. Quality
measures adopted for the IPFQR Program measure set for a previous
payment determination year are retained for use in subsequent payment
determination years, except when they are removed, suspended, or
modified as set forth in paragraph (3) of this section.
(3) Measure removal, suspension, or modification through the
rulemaking process. CMS will use the regular rulemaking process to
remove, suspend, or modify quality measures in the IPFQR Program to
allow for public comment.
(i) Factors for consideration in removal or replacement of quality
measures. CMS will weigh whether to remove or modify measures based on
the following factors:
(A) Factor 1: Measure performance among IPFs is so high and
unvarying that meaningful distinctions and improvements in performance
can no longer be made;
(B) Factor 2: Measure does not align with current clinical
guidelines or practice;
(C) Factor 3: Measure can be replaced by a more broadly applicable
measure (across settings or populations) or a measure that is more
proximal in time to desired patient outcomes for the particular topic;
(D) Factor 4: Measure performance or improvement does not result in
better patient outcomes;
(E) Factor 5: Measure can be replaced by a measure that is more
strongly associated with desired patient outcomes for the particular
topic;
(F) Factor 6: Measure collection or public reporting leads to
negative unintended consequences other than patient harm;
(G) Factor 7: Measure is not feasible to implement as specified;
and
(H) Factor 8: The costs associated with a measure outweigh the
benefit of its continued use in the program.
(ii) Retention. CMS may retain a quality measure that meets one or
more of the measure removal factors described in paragraph (i) of this
subsection if the continued collection of data on the quality measure
would align with other CMS and HHS policy goals, align with other CMS
programs, or support efforts to move IPFs toward reporting electronic
measures.
(f) Extraordinary circumstances exception. CMS may grant an
exception to one or more data submissions deadlines and requirements in
the event of extraordinary circumstances beyond the control of the IPF,
such as when an act of nature affects an entire region or locale or a
systemic problem with one of CMS's data collection systems directly or
indirectly affects data submission. CMS may grant an exception as
follows:
(1) Upon request by the IPF.
(2) At the discretion of CMS. CMS may grant exceptions to IPFs that
have not requested them when CMS determines that an extraordinary
circumstance has occurred.
[[Page 51162]]
(g) Public reporting of IPFQR Program data. Data that an IPF
submits to CMS for the IPFQR Program will be made publicly available on
a CMS website after providing the IPF an opportunity to review the data
to be made public. IPFs will have a period of 30 days to review and
submit corrections to errors resulting from CMS calculations prior to
the data being made public.
Xavier Becerra,
Secretary, Department of Health and Human Services.
[FR Doc. 2023-16083 Filed 7-27-23; 4:15 pm]
BILLING CODE 4120-01-P