Medicare and Medicaid Programs; CY 2018 Home Health Prospective Payment System Rate Update and CY 2019 Case-Mix Adjustment Methodology Refinements; Home Health Value-Based Purchasing Model; and Home Health Quality Reporting Requirements, 51676-51752 [2017-23935]
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Contact Joan Proctor, (410) 786–0949
for information about the Home Health
Quality Reporting Program (HH QRP).
SUPPLEMENTARY INFORMATION: Wage
index addenda will be available only
through the internet on the CMS Web
site at: https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
HomeHealthPPS/coding_billing.html.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 484
[CMS–1672–F]
RIN 0938–AT01
Table of Contents
Medicare and Medicaid Programs; CY
2018 Home Health Prospective
Payment System Rate Update and CY
2019 Case-Mix Adjustment
Methodology Refinements; Home
Health Value-Based Purchasing Model;
and Home Health Quality Reporting
Requirements
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Final rule.
AGENCY:
This final rule updates the
home health prospective payment
system (HH PPS) payment rates,
including the national, standardized 60day episode payment rates, the national
per-visit rates, and the non-routine
medical supply (NRS) conversion factor,
effective for home health episodes of
care ending on or after January 1, 2018.
This rule also: Updates the HH PPS
case-mix weights using the most
current, complete data available at the
time of rulemaking; implements the
third year of a 3-year phase-in of a
reduction to the national, standardized
60-day episode payment to account for
estimated case-mix growth unrelated to
increases in patient acuity (that is,
nominal case-mix growth) between
calendar year (CY) 2012 and CY 2014;
and discusses our efforts to monitor the
potential impacts of the rebasing
adjustments that were implemented in
CY 2014 through CY 2017. In addition,
this rule finalizes changes to the Home
Health Value-Based Purchasing
(HHVBP) Model and to the Home Health
Quality Reporting Program (HH QRP).
We are not finalizing the
implementation of the Home Health
Groupings Model (HHGM) in this final
rule.
DATES: These regulations are effective
on January 1, 2018.
FOR FURTHER INFORMATION CONTACT:
For general information about the
Home Health Prospective Payment
System (HH PPS), please send your
inquiry via email to:
HomehealthPolicy@cms.hhs.gov.
For information about the Home
Health Value-Based Purchasing
(HHVBP) Model, please send your
inquiry via email to: HHVBPquestions@
cms.hhs.gov.
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SUMMARY:
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I. Executive Summary
A. Purpose
B. Summary of the Major Provisions
C. Summary of Costs and Benefits
II. Background
A. Statutory Background
B. Current System for Payment of Home
Health Services
C. Updates to the Home Health Prospective
Payment System
D. Report to Congress: Home Health Study
on Access to Care for Vulnerable Patient
Populations and Subsequent Research
and Analyses
III. Provisions of the Proposed Rule: Payment
Under the Home Health Prospective
Payment System (HH PPS) and
Responses to Comments
A. Monitoring for Potential Impacts—
Affordable Care Act Rebasing
Adjustments
B. CY 2018 HH PPS Case-Mix Weights
C. CY 2018 Home Health Payment Rate
Update
D. Payments for High-Cost Outliers Under
the HH PPS
E. Proposed Implementation of the Home
Health Groupings Model (HHGM) for CY
2019
IV. Provisions of the Home Health ValueBased Purchasing (HHVBP) Model and
Responses to Comments
A. Background
B. Quality Measures
C. Quality Measures for Future
Consideration
V. Updates to the Home Health Care Quality
Reporting Program (HH QRP)
A. Background and Statutory Authority
B. General Considerations Used for the
Selection of Quality Measures for the HH
QRP
C. Accounting for Social Risk Factors in
the HH QRP
D. Removal From OASIS
E. Collection of Standardized Patient
Assessment Data Under the HH QRP
F. HH QRP Quality Measures Beginning
With the CY 2020 HH QRP
G. HH QRP Quality Measures and Measure
Concepts Under Consideration for Future
Years
H. Standardized Patient Assessment Data
I. Form, Manner, and Timing of Data
Submission Under the HH QRP
J. Other Provisions for the CY 2019 HH
QRP and Subsequent Years
K. Policies Regarding Public Display of
Quality Measure Data for the HH QRP
L. Mechanism for Providing Confidential
Feedback Reports to HHAs
M. Home Health Care CAHPS® Survey
(HHCAHPS)
VI. Collection of Information Requirements
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A. Statutory Requirement for Solicitation
of Comments
B. Collection of Information Requirements
for the HH QRP
C. Submission of PRA-Related Comments
VII. Regulatory Impact Analysis
A. Statement of Need
B. Overall Impact
C. Detailed Economic Analysis
D. Accounting Statement and Table
E. Reducing Regulation and Controlling
Regulatory Costs
F. Conclusion
VIII. Federalism Analysis
Regulation Text
Acronyms
In addition, because of the many
terms to which we refer by abbreviation
in this final rule, we are listing these
abbreviations and their corresponding
terms in alphabetical order below:
ACH LOS Acute Care Hospital Length of
Stay
ADL Activities of Daily Living
AM–PAC Activity Measure for Post-Acute
Care
APR DRG All-Patient Refined DiagnosisRelated Group
APU Annual Payment Update
ASPE Assistant Secretary for Planning and
Evaluation
BBA Balanced Budget Act of 1997, Public
Law 105–33
BBRA Medicare, Medicaid, and SCHIP
Balanced Budget Refinement Act of 1999,
(Pub. L. 106–113)
BIMS Brief Interview for Mental Status
BLS Bureau of Labor Statistics
CAD Coronary Artery Disease
CAH Critical Access Hospital
CAM Confusion Assessment Method
CARE Continuity Assessment Record and
Evaluation
CASPER Certification and Survey Provider
Enhanced Reports
CBSA Core-Based Statistical Area
CCN CMS Certification Number
CHF Congestive Heart Failure
CMI Case-Mix Index
CMP Civil Money Penalty
CMS Centers for Medicare & Medicaid
Services
CoPs Conditions of Participation
COPD Chronic Obstructive Pulmonary
Disease
CVD Cardiovascular Disease
CY Calendar Year
DM Diabetes Mellitus
DRA Deficit Reduction Act of 2005, Public
Law 109–171, enacted February 8, 2006
DRG Diagnosis-Related Group
DTI Deep Tissue Injury
EOC End of Care
FDL Fixed Dollar Loss
FI Fiscal Intermediaries
FR Federal Register
FY Fiscal Year
HAVEN Home Assessment Validation and
Entry System
HCC Hierarchical Condition Categories
HCIS Health Care Information System
HH Home Health
HHA Home Health Agency
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HHCAHPS Home Health Care Consumer
Assessment of Healthcare Providers and
Systems Survey
HH PPS Home Health Prospective Payment
System
HHGM Home Health Groupings Model
HHQRP Home Health Quality Reporting
Program
HHRG Home Health Resource Group
HHVBP Home Health Value-Based
Purchasing
HIPPS Health Insurance Prospective
Payment System
HVBP Hospital Value-Based Purchasing
IADL Instrumental Activities of Daily
Living
ICD–9–CM International Classification of
Diseases, Ninth Revision, Clinical
Modification
ICD–10–CM International Classification of
Diseases, Tenth Revision, Clinical
Modification
IH Inpatient Hospitalization
IMPACT Act Improving Medicare PostAcute Care Transformation Act of 2014
(Pub. L. 113–185)
IPPS [Acute Care Hospital] Inpatient
Prospective Payment System
IPR Interim Performance Report
IRF Inpatient Rehabilitation Facility
IRF–PAI IRF Patient Assessment Instrument
IV Intravenous
LCDS LTCH CARE Data Set
LEF Linear Exchange Function
LTCH Long-Term Care Hospital
LUPA Low-Utilization Payment Adjustment
MACRA Medicare Access and CHIP
Reauthorization Act of 2015
MAP Measure Applications Partnership
MDS Minimum Data Set
MFP Multifactor productivity
MMA Medicare Prescription Drug,
Improvement, and Modernization Act of
2003, Public Law 108–173, enacted
December 8, 2003
MSA Metropolitan Statistical Area
MSS Medical Social Services
NQF National Quality Forum
NQS National Quality Strategy
NRS Non-Routine Supplies
OASIS Outcome and Assessment
Information Set
OBRA Omnibus Budget Reconciliation Act
of 1987, Public Law 100–2–3, enacted
December 22, 1987
OCESAA Omnibus Consolidated and
Emergency Supplemental Appropriations
Act, Public Law 105–277, enacted October
21, 1998
OES Occupational Employment Statistics
OIG Office of Inspector General
OLS Ordinary Least Squares
OT Occupational Therapy
OMB Office of Management and Budget
PAC Post-Acute Care
PAC–PRD Post-Acute Care Payment Reform
Demonstration
PAMA Protecting Access to Medicare Act of
2014
PEP Partial Episode Payment Adjustment
PHQ–2 Patient Health Questionnaire-2
PPOC Primary Point of Contact
PPS Prospective Payment System
PRA Paperwork Reduction Act
PRRB Provider Reimbursement Review
Board
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PT Physical Therapy
PY Performance Year
QAP Quality Assurance Plan
QIES Quality Improvement Evaluation
System
QRP Quality Reporting Program
RAP Request for Anticipated Payment
RF Renal Failure
RFA Regulatory Flexibility Act, Public Law
96—354
RHHIs Regional Home Health
Intermediaries
RIA Regulatory Impact Analysis
ROC Resumption of Care
SAF Standard Analytic File
SLP Speech-Language Pathology
SN Skilled Nursing
SNF Skilled Nursing Facility
SOC Start of Care
SSI Surgical Site Infection
TEP Technical Expert Panel
TPS Total Performance Score
UMRA Unfunded Mandates Reform Act of
1995
VAD Vascular Access Device
VBP Value-Based Purchasing
I. Executive Summary
A. Purpose
This final rule updates the payment
rates for home health agencies (HHAs)
for calendar year (CY) 2018, as required
under section 1895(b) of the Social
Security Act (the Act). This final rule
also updates the case-mix weights under
section 1895(b)(4)(A)(i) and (b)(4)(B) of
the Act for CY 2018 and implements a
0.97 percent reduction to the national,
standardized 60-day episode payment
amount to account for case-mix growth
unrelated to increases in patient acuity
(that is, nominal case-mix growth)
between CY 2012 and CY 2014, under
the authority of section 1895(b)(3)(B)(iv)
of the Act. Additionally, this rule
finalizes changes to the Home Health
Value Based Purchasing (HHVBP)
Model under the authority of section
1115A of the Act, and Home Health
Quality Reporting Program (HH QRP)
requirements under the authority of
section 1895(b)(3)(B)(v) of the Act. We
are not finalizing the implementation of
the Home Health Groupings Model
(HHGM) in this final rule. We received
a number of comments from the public
that we would like to take into further
consideration.
B. Summary of the Major Provisions
In the CY 2015 HH PPS final rule (79
FR 66072), we finalized our proposal to
recalibrate the case-mix weights every
year with the most current and complete
data available at the time of rulemaking.
In section III.B. of this final rule, we are
recalibrating the HH PPS case-mix
weights, using the most current cost and
utilization data available, in a budgetneutral manner. Also in section III.B. of
this final rule, as finalized in the CY
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2016 HH PPS final rule (80 FR 68624),
we are implementing a reduction to the
national, standardized 60-day episode
payment rate for CY 2018 of 0.97
percent to account for estimated casemix growth unrelated to increases in
patient acuity (that is, nominal case-mix
growth) between CY 2012 and CY 2014.
In section III.C. of this final rule, we
update the payment rates under the HH
PPS by 1 percent for CY 2018 in
accordance with section 411(d) of the
Medicare Access and CHIP
Reauthorization Act of 2015 (MACRA)
(Pub. L. 114–10, enacted April 16, 2015)
which amended section 1895(b)(3)(B) of
the Act. Additionally, section III.C. of
this final rule, updates the CY 2018
home health wage index using FY 2014
hospital cost report data. In section
III.D. of this final rule, we note that the
fixed-dollar loss ratio remains 0.55 for
CY 2018 to pay up to, but no more than,
2.5 percent of total payments as outlier
payments, as required by section
1895(b)(5)(A) of the Act.
In section IV of this final rule, we are
finalizing changes to the Home Health
Value-Based Purchasing (HHVBP)
Model implemented January 1, 2016.
We are amending the definition of
‘‘applicable measure’’ to mean a
measure for which a competing HHA
has provided a minimum of 40
completed surveys for Home Health
Care Consumer Assessment of
Healthcare Providers and Systems
(HHCAHPS) measures, beginning with
Performance Year (PY) 1, for purposes
of receiving a performance score for any
of the HHCAHPS measures, and for PY
3 and subsequent years, we are
finalizing the removal of the Outcome
and Assessment Information Set
(OASIS)-based measure, Drug Education
on All Medications Provided to Patient/
Caregiver during All Episodes of Care,
from the set of applicable measures.
In section V. of this final rule, we are
finalizing updates to the Home Health
Quality Reporting Program, including:
The replacement of one quality measure
and the adoption of two new quality
measures, data submission
requirements, exception and extension
requirements, and reconsideration and
appeals procedures. We have also
finalized the removal of 235 data
elements from 33 current OASIS items,
effective with all HHA assessments on
or after January 1, 2019. We are not
finalizing the standardized patient
assessment data elements that we
proposed to adopt for three of the five
categories under section 1899B(b)(1)(B)
of the Act: Cognitive Function and
Mental Status; Special Services,
Treatments, and Interventions; and
Impairments.
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C. Summary of Costs and Benefits
TABLE 1—SUMMARY OF COSTS AND TRANSFERS
Provision description
Costs
Transfers
CY 2018 HH PPS Payment Rate
Update.
CY 2018 HHVBP Model ..................
........................................................
The overall economic impact of the HH PPS payment rate update is
an estimated ¥$80 million (¥0.4 percent) in payments to HHAs.
The overall economic impact of the HHVBP Model provision for CY
2018 through 2022 is an estimated $378 million in total savings
from a reduction in unnecessary hospitalizations and SNF usage
as a result of greater quality improvements in the HH industry
(none of which is attributable to the changes finalized in this final
rule). As for payments to HHAs, there are no aggregate increases
or decreases expected to be applied to the HHAs competing in the
model.
CY 2019 HH QRP ...........................
........................................................
The overall economic impact of
the HH QRP changes is a savings to HHAs of an estimated
$146.0 million, beginning January 1, 2019.
II. Background
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A. Statutory Background
The Balanced Budget Act of 1997
(BBA) (Pub. L. 105–33, enacted August
5, 1997), significantly changed the way
Medicare pays for Medicare home
health services. Section 4603 of the BBA
mandated the development of the HH
PPS. Until the implementation of the
HH PPS on October 1, 2000, HHAs
received payment under a retrospective
reimbursement system.
Section 4603(a) of the BBA mandated
the development of a HH PPS for all
Medicare-covered home health services
provided under a plan of care (POC) that
were paid on a reasonable cost basis by
adding section 1895 of the Act, entitled
‘‘Prospective Payment For Home Health
Services.’’ Section 1895(b)(1) of the Act
requires the Secretary to establish a HH
PPS for all costs of home health services
paid under Medicare. Section 1895(b)(2)
of the Act requires that, in defining a
prospective payment amount, the
Secretary shall consider an appropriate
unit of service and the number, type,
and duration of visits provided within
that unit, potential changes in the mix
of services provided within that unit
and their cost, and a general system
design that provides for continued
access to quality services.
Section 1895(b)(3)(A) of the Act
requires the following: (1) The
computation of a standard prospective
payment amount include all costs for
HH services covered and paid for on a
reasonable cost basis and that such
amounts be initially based on the most
recent audited cost report data available
to the Secretary; and (2) the
standardized prospective payment
amount be adjusted to account for the
effects of case-mix and wage levels
among HHAs.
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Section 1895(b)(3)(B) of the Act
addresses the annual update to the
standard prospective payment amounts
by the home health applicable
percentage increase. Section 1895(b)(4)
of the Act governs the payment
computation. Sections 1895(b)(4)(A)(i)
and (b)(4)(A)(ii) of the Act require the
standard prospective payment amount
to be adjusted for case-mix and
geographic differences in wage levels.
Section 1895(b)(4)(B) of the Act requires
the establishment of an appropriate
case-mix change adjustment factor for
significant variation in costs among
different units of services.
Similarly, section 1895(b)(4)(C) of the
Act requires the establishment of wage
adjustment factors that reflect the
relative level of wages, and wage-related
costs applicable to home health services
furnished in a geographic area
compared to the applicable national
average level. Under section
1895(b)(4)(C) of the Act, the wageadjustment factors used by the Secretary
may be the factors used under section
1886(d)(3)(E) of the Act.
Section 1895(b)(5) of the Act gives the
Secretary the option to make additions
or adjustments to the payment amount
otherwise paid in the case of outliers
due to unusual variations in the type or
amount of medically necessary care.
Section 3131(b)(2) of the Affordable
Care Act revised section 1895(b)(5) of
the Act so that total outlier payments in
a given year would not exceed 2.5
percent of total payments projected or
estimated. The provision also made
permanent a 10 percent agency-level
outlier payment cap.
In accordance with the statute, as
amended by the BBA, we published a
final rule in the July 3, 2000 Federal
Register (65 FR 41128) to implement the
HH PPS legislation. The July 2000 final
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rule established requirements for the
new HH PPS for home health services
as required by section 4603 of the BBA,
as subsequently amended by section
5101 of the Omnibus Consolidated and
Emergency Supplemental
Appropriations Act for Fiscal Year 1999
(OCESAA), (Pub. L. 105–277, enacted
October 21, 1998); and by sections 302,
305, and 306 of the Medicare, Medicaid,
and SCHIP Balanced Budget Refinement
Act of 1999, (BBRA) (Pub. L. 106–113,
enacted November 29, 1999). The
requirements include the
implementation of a HH PPS for home
health services, consolidated billing
requirements, and a number of other
related changes. The HH PPS described
in that rule replaced the retrospective
reasonable cost-based system that was
used by Medicare for the payment of
home health services under Part A and
Part B. For a complete and full
description of the HH PPS as required
by the BBA, see the July 2000 HH PPS
final rule (65 FR 41128 through 41214).
Section 5201(c) of the Deficit
Reduction Act of 2005 (DRA) (Pub. L.
109–171, enacted February 8, 2006)
added new section 1895(b)(3)(B)(v) to
the Act, requiring HHAs to submit data
for purposes of measuring health care
quality, and links the quality data
submission to the annual applicable
percentage increase. This data
submission requirement is applicable
for CY 2007 and each subsequent year.
If an HHA does not submit quality data,
the home health market basket
percentage increase is reduced by 2
percentage points. In the November 9,
2006 Federal Register (71 FR 65884,
65935), we published a final rule to
implement the pay-for-reporting
requirement of the DRA, which was
codified at § 484.225(h) and (i) in
accordance with the statute. The pay-
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for-reporting requirement was
implemented on January 1, 2007.
The Affordable Care Act made
additional changes to the HH PPS. One
of the changes in section 3131 of the
Affordable Care Act is the amendment
to section 421(a) of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) (Pub.
L. 108–173, enacted on December 8,
2003) as amended by section 5201(b) of
the DRA. Section 421(a) of the MMA, as
amended by section 3131 of the
Affordable Care Act, requires that the
Secretary increase, by 3 percent, the
payment amount otherwise made under
section 1895 of the Act, for HH services
furnished in a rural area (as defined in
section 1886(d)(2)(D) of the Act) with
respect to episodes and visits ending on
or after April 1, 2010, and before
January 1, 2016.
Section 210 of the MACRA amended
section 421(a) of the MMA to extend the
rural add-on for 2 more years. Section
421(a) of the MMA, as amended by
section 210 of the MACRA, requires that
the Secretary increase, by 3 percent, the
payment amount otherwise made under
section 1895 of the Act, for home health
services provided in a rural area (as
defined in section 1886(d)(2)(D) of the
Act) with respect to episodes and visits
ending on or after April 1, 2010, and
before January 1, 2018. Section 411(d) of
MACRA amended section 1895(b)(3)(B)
of the Act such that for home health
payments for CY 2018, the market
basket percentage increase shall be 1
percent.
B. Current System for Payment of Home
Health Services
Generally, Medicare currently makes
payment under the HH PPS on the basis
of a national, standardized 60-day
episode payment rate that is adjusted for
the applicable case-mix and wage index.
The national, standardized 60-day
episode rate includes the six home
health disciplines (skilled nursing,
home health aide, physical therapy,
speech-language pathology,
occupational therapy, and medical
social services). Payment for nonroutine supplies (NRS) is not part of the
national, standardized 60-day episode
rate, but is computed by multiplying the
relative weight for a particular NRS
severity level by the NRS conversion
factor. Payment for durable medical
equipment covered under the HH
benefit is made outside the HH PPS
payment system. To adjust for case-mix,
the HH PPS uses a 153-category casemix classification system to assign
patients to a home health resource
group (HHRG). The clinical severity
level, functional severity level, and
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service utilization are computed from
responses to selected data elements in
the OASIS assessment instrument and
are used to place the patient in a
particular HHRG. Each HHRG has an
associated case-mix weight which is
used in calculating the payment for an
episode. Therapy service use is
measured by the number of therapy
visits provided during the episode and
can be categorized into nine visit level
categories (or thresholds): 0 to 5; 6; 7 to
9; 10; 11 to 13; 14 to 15; 16 to 17; 18
to 19; and 20 or more visits.
For episodes with four or fewer visits,
Medicare pays national per-visit rates
based on the discipline(s) providing the
services. An episode consisting of four
or fewer visits within a 60-day period
receives what is referred to as a lowutilization payment adjustment (LUPA).
Medicare also adjusts the national
standardized 60-day episode payment
rate for certain intervening events that
are subject to a partial episode payment
adjustment (PEP adjustment). For
certain cases that exceed a specific cost
threshold, an outlier adjustment may
also be available.
C. Updates to the Home Health
Prospective Payment System
As required by section 1895(b)(3)(B)
of the Act, we have historically updated
the HH PPS rates annually in the
Federal Register. The August 29, 2007
final rule with comment period set forth
an update to the 60-day national
episode rates and the national per-visit
rates under the HH PPS for CY 2008.
The CY 2008 HH PPS final rule
included an analysis performed on CY
2005 home health claims data, which
indicated a 12.78 percent increase in the
observed case-mix since 2000. Case-mix
represents the variations in conditions
of the patient population served by the
HHAs. Subsequently, a more detailed
analysis was performed on the 2005
case-mix data to evaluate if any portion
of the 12.78 percent increase was
associated with a change in the actual
clinical condition of home health
patients. We identified 8.03 percent of
the total case-mix change as real, and
therefore, decreased the 12.78 percent of
total case-mix change by 8.03 percent to
get a final nominal case-mix increase
measure of 11.75 percent (0.1278 *
(1¥0.0803) = 0.1175).
To account for the changes in casemix that were not related to an
underlying change in patient health
status, we implemented a reduction,
over 4 years, to the national,
standardized 60-day episode payment
rates. That reduction was to be 2.75
percent per year for 3 years beginning in
CY 2008 and 2.71 percent for the fourth
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year in CY 2011. In the CY 2011 HH PPS
final rule (76 FR 68532), we updated our
analyses of case-mix change and
finalized a reduction of 3.79 percent,
instead of 2.71 percent, for CY 2011 and
deferred finalizing a payment reduction
for CY 2012 until further study of the
case-mix change data and methodology
was completed.
In the CY 2012 HH PPS final rule (76
FR 68526), we updated the 60-day
national episode rates and the national
per-visit rates. In addition, as discussed
in the CY 2012 HH PPS final rule (76
FR 68528), our analysis indicated that
there was a 22.59 percent increase in
overall case-mix from 2000 to 2009 and
that only 15.76 percent of that overall
observed case-mix percentage increase
was due to real case-mix change. As a
result of our analysis, we identified a
19.03 percent nominal increase in casemix. At that time, to fully account for
the 19.03 percent nominal case-mix
growth identified from 2000 to 2009, we
finalized a 3.79 percent payment
reduction in CY 2012 and a 1.32 percent
payment reduction for CY 2013.
In the CY 2013 HH PPS final rule (77
FR 67078), we implemented the 1.32
percent reduction to the payment rates
for CY 2013 finalized the previous year,
to account for nominal case-mix growth
from 2000 through 2010. When taking
into account the total measure of casemix change (23.90 percent) and the
15.97 percent of total case-mix change
estimated as real from 2000 to 2010, we
obtained a final nominal case-mix
change measure of 20.08 percent from
2000 to 2010 (0.2390 * (1¥0.1597) =
0.2008). To fully account for the
remainder of the 20.08 percent increase
in nominal case-mix beyond that which
was accounted for in previous payment
reductions, we estimated that the
percentage reduction to the national,
standardized 60-day episode rates for
nominal case-mix change would be 2.18
percent. Although we considered
proposing a 2.18 percent reduction to
account for the remaining increase in
measured nominal case-mix, we
finalized the 1.32 percent payment
reduction to the national, standardized
60-day episode rates in the CY 2012 HH
PPS final rule (76 FR 68532).
Section 3131(a) of the Affordable Care
Act requires that, beginning in CY 2014,
we apply an adjustment to the national,
standardized 60-day episode rate and
other amounts that reflect factors such
as changes in the number of visits in an
episode, the mix of services in an
episode, the level of intensity of services
in an episode, the average cost of
providing care per episode, and other
relevant factors. Additionally, we must
phase in any adjustment over a 4-year
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period in equal increments, not to
exceed 3.5 percent of the amount (or
amounts) as of the date of enactment of
the Affordable Care Act, and fully
implement the rebasing adjustments by
CY 2017. The statute specifies that the
maximum rebasing adjustment is to be
no more than 3.5 percent per year of the
CY 2010 rates. Therefore, in the CY
2014 HH PPS final rule (78 FR 72256)
for each year, CY 2014 through CY 2017,
we finalized a fixed-dollar reduction to
the national, standardized 60-day
episode payment rate of $80.95 per year,
increases to the national per-visit
payment rates per year, and a decrease
to the NRS conversion factor of 2.82
percent per year. We also finalized three
separate LUPA add-on factors for skilled
nursing, physical therapy, and speechlanguage pathology and removed 170
diagnosis codes from assignment to
diagnosis groups in the HH PPS
Grouper. In the CY 2015 HH PPS final
rule (79 FR 66032), we implemented the
second year of the 4-year phase-in of the
rebasing adjustments to the HH PPS
payment rates and made changes to the
HH PPS case-mix weights. In addition,
we simplified the face-to-face encounter
regulatory requirements and the therapy
reassessment timeframes.
In the CY 2016 HH PPS final rule (80
FR 68624), we implemented the third
year of the 4-year phase-in of the
rebasing adjustments to the national,
standardized 60-day episode payment
amount, the national per-visit rates and
the NRS conversion factor (as outlined
previously). In the CY 2016 HH PPS
final rule, we also recalibrated the HH
PPS case-mix weights, using the most
current cost and utilization data
available, in a budget-neutral manner
and finalized reductions to the national,
standardized 60-day episode payment
rate in CY 2016, CY 2017, and CY 2018
of 0.97 percent in each year to account
for estimated case-mix growth unrelated
to increases in patient acuity (that is,
nominal case-mix growth) between CY
2012 and CY 2014. Finally, section
421(a) of the MMA, as amended by
section 210 of the MACRA, extended
the payment increase of 3 percent for
HH services provided in rural areas (as
defined in section 1886(d)(2)(D) of the
Act) to episodes or visits ending before
January 1, 2018.
In the CY 2017 HH PPS final rule (81
FR 76702), we implemented the last
year of the 4-year phase-in of the
rebasing adjustments to the national,
standardized 60-day episode payment
amount, the national per-visit rates and
the NRS conversion factor (as outlined
previously). We also finalized changes
to the methodology used to calculate
outlier payments under the authority of
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section 1895(b)(5) of the Act. Lastly, in
accordance with section 1834(s) of the
Act, as added by section 504(a) of the
Consolidated Appropriations Act, 2016
(Pub. L. 114–113, enacted December 18,
2015), we implemented changes in
payment for furnishing Negative
Pressure Wound Therapy (NPWT) using
a disposable device for patients under a
home health plan of care for which
payment would otherwise be made
under section 1895(b) of the Act.
D. Report to Congress: Home Health
Study on Access to Care for Vulnerable
Patient Populations and Subsequent
Research and Analyses
Section 3131(d) of the Affordable Care
Act required CMS to conduct a study on
home health agency costs involved with
providing ongoing access to care to lowincome Medicare beneficiaries or
beneficiaries in medically underserved
areas, and in treating beneficiaries with
varying levels of severity of illness and
submit a report to Congress. As
discussed in the CY 2016 HH PPS
proposed rule (80 FR 39840) and the CY
2017 HH PPS proposed rule (81 FR
43744), the findings from the Report to
Congress on the ‘‘Medicare Home
Health Study: An Investigation on
Access to Care and Payment for
Vulnerable Patient Populations,’’ found
that payment accuracy could be
improved under the current payment
system, particularly for patients with
certain clinical characteristics requiring
more nursing care than therapy.1
The research for the Report to
Congress, released in December 2014,
consisted of extensive analysis of both
survey and administrative data. The
CMS-developed surveys were given to
physicians who referred vulnerable
patient populations to Medicare home
health and to Medicare-certified HHAs.2
The response rates were 72 percent and
59 percent for the HHA and physician
surveys, respectively. The results of the
survey revealed that over 80 percent of
respondent HHAs and over 90 percent
of respondent physicians reported that
access to home health care for Medicare
fee-for-service beneficiaries in their
local area was excellent or good. When
survey respondents reported access
issues, specifically their inability to
place or admit Medicare fee-for-service
patients into home health, the most
1 The Report to Congress can be found in its
entirety at https://www.cms.gov/Medicare/
Medicare-Fee-for-ServicePayment/HomeHealthPPS/
Downloads/HH-Report-to-Congress.pdf.
2 For the purposes of the surveys, ‘‘vulnerable
patient populations’’ were defined as beneficiaries
who were either eligible for the Part D low-income
subsidy (LIS) 27 or residing in a health professional
shortage area (HPSA).
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common reason reported (64 percent of
respondent HHAs surveyed) was that
the patients did not qualify for the
Medicare home health benefit. HHAs
and physicians also cited family or
caregiver issues as an important
contributing factor in the inability to
admit or place patients. Only 17.2
percent of HHAs and 16.7 percent of
physicians reported insufficient
payment as an important contributing
factor in the inability to admit or place
patients. The results of the CMSconducted surveys suggested that CMS’
ability to improve access for certain
vulnerable patient populations through
payment policy may be limited.
However, we are able to revise the casemix system to minimize differences in
payment that could potentially be
serving as a barrier to receiving care. In
the near future, we intend to better align
payment with resource use so that it
reduces HHAs’ financial incentives to
select certain patients over others.
We also performed an analysis of
Medicare administrative data (CY 2010
Medicare claims and cost report data)
and calculated margins for episodes of
care. This was done because margin
differences associated with patient
clinical and social characteristics can
indicate whether financial incentives
exist in the current HH PPS to provide
home health care for certain types of
patients over others. Lower margins, if
systematically associated with care for
vulnerable patient populations, may
indicate financial disincentives for
HHAs to admit these patients,
potentially creating access to care
issues. The findings from the data
analysis found that certain patient
characteristics appear to be strongly
associated with margin levels, and thus
may create financial incentives to select
certain patients over others. Margins
were estimated to be lower for patients
who required parenteral nutrition, who
had traumatic wounds or ulcers, or
required substantial assistance in
bathing. For example, in CY 2010,
episodes for patients with parenteral
nutrition were, on average, associated
with a $178.53 lower margin than
episodes for patients without parenteral
nutrition. Given that these variables are
already included in the HH PPS casemix system, the results indicated that
modifications to the way the current
case-mix system accounts for resource
use differences may be needed to
mitigate any financial incentives to
select certain patients over others.
Margins were also lower for
beneficiaries who were admitted after
acute or post-acute stays or who had
certain poorly-controlled clinical
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conditions, such as poorly controlled
pulmonary disorders, indicating that
accounting for additional patient
characteristic variables in the HH PPS
case-mix system may also reduce
financial incentives to select certain
types of patients over others. More
information on the results from the
home health study required by section
3131(d) of the Affordable Care Act can
be found in the Report to Congress on
the ‘‘Medicare Home Health Study: An
Investigation on Access to Care and
Payment for Vulnerable Patient
Populations’’ available at https://
www.cms.gov/center/provider-Type/
home-Health-Agency-HHA-Center.html.
Section 3131(d)(5) of the Affordable
Care Act authorized the Secretary to
determine whether it would be
appropriate to conduct a Medicare
demonstration project based on the
result of the home health study. If the
Secretary determined it was appropriate
to conduct the demonstration project
under this subsection, the Secretary was
to conduct the project for a 4-year
period beginning not later than January
1, 2015. We did not determine that it
was appropriate to conduct a
demonstration project based on the
findings from the home health study.
Rather, the findings from the home
health study suggested that follow-on
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work should be conducted to better
align payments with costs under the
authority of section 1895 of the Act.
In addition to the findings from the
Report to Congress on the ‘‘Medicare
Home Health Study: An Investigation on
Access to Care and Payment for
Vulnerable Patient Populations,’’
concerns have also been raised about
the use of therapy thresholds in the
current payment system. Under the
current payment system, HHAs receive
higher payments for providing more
therapy visits once certain thresholds
are reached. As a result, the average
number of therapy visits per 60-day
episode of care have increased since the
implementation of the HH PPS, while
the number of skilled nursing and home
health aide visits have decreased over
the same time period (82 FR 35280
(Figure 3)). A study examining an
option of using predicted, rather than
actual, therapy visits in the home health
found that in 2013, 58 percent of home
health episodes included some therapy
services, and these episodes accounted
for 72 percent of all Medicare home
health payments.3 Figure 1, from that
3 Fout
B, Plotzke M, Christian T. (2016). Using
Predicted Therapy Visits in the Medicare Home
Health Prospective Payment System. Home Health
Care Management & Practice, 29(2), 81–90. https://
journals.sagepub.com/doi/abs/10.1177/
1084822316678384.
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51681
study, demonstrates that the percentage
of episodes, and the average episode
payment by the number of therapy visits
for episodes with at least one therapy
visit in 2013 increased sharply in
therapy provision just over payment
thresholds at 6, 7, and 16. According to
the study, the presence of sharp
increases in the percentage of episodes
just above payment thresholds suggests
a response to financial incentives in the
home health payment system. Similarly,
between 2008 and 2013, MedPAC
reported a 26 percent increase in the
number of episodes with at least 6
therapy visits, compared with a 1
percent increase in the number of
episodes with 5 or fewer therapy visits.4
CMS analysis demonstrates that the
average share of therapy visits across all
60-day episodes of care increased from
9 percent of all visits in 1997, prior to
the implementation of the HH PPS (see
64 FR 58151), to 39 percent of all visits
in 2015 (82 FR 35277 through 35278
(Table 2)).
4 Medicare Payment Advisory Commission
(MedPAC). ‘‘Home Health Care Services.’’ Report to
Congress: Medicare Payment Policy. Washington,
DC, March 2015. P. 223. Accessed on March 28,
2017 at: https://www.medpac.gov/docs/defaultsource/reports/mar2015_entirereport_revised
.pdf?sfvrsn=0.
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Figure 1 suggests that HHAs may be
responding to financial incentives in the
home health payment system when
making care plan decisions.
Additionally, an investigation into the
therapy practices of the four largest
publically-traded home health
companies, conducted by the Senate
Committee on Finance in 2010, found
that three out of the four companies
investigated ‘‘encouraged therapists to
target the most profitable number of
therapy visits, even when patient need
alone may not have justified such
patterns’’.5 The Senate Committee on
Finance investigation also highlighted
the abrupt and dramatic responses the
home health industry has taken to
maximize reimbursement under the
therapy threshold models (both the
original 10-visit threshold model and
under the revised thresholds
implemented in the CY 2008 HH PPS
final rule (72 FR 49762)). The report
noted that, under the HH PPS, HHAs
have broad discretion over the number
of therapy visits to provide patients, and
therefore, have control of the singlelargest variable in determining
reimbursement and overall margins. The
report recommended that CMS closely
examine a future payment approach that
focuses on patient well-being and health
characteristics, rather than the
numerical utilization measures.
MedPAC also continues to
recommend the removal of the therapy
thresholds used for determining
payment from the HH PPS, as it believes
that such thresholds run counter to the
goals of a prospective payment system,
create financial incentives that detract
from a focus on patient characteristics
and care needs when agencies are
setting plans of care for their patients,
and incentivize unnecessary therapy
utilization. For the average HHA,
according to MedPAC, the increase in
payment for therapy visits rises faster
than costs, resulting in financial
incentives for HHAs to overprovide
therapy services.6 HHAs that provide
more therapy episodes tend to be more
profitable and this higher profitability
and rapid growth in the number of
therapy episodes suggest that financial
incentives are causing agencies to favor
therapy services when possible.7
Eliminating therapy as a payment factor
will base home health payment solely
on patient characteristics, which is a
more patient-focused approach to
payment, as recommended by both
MedPAC and previously by the Senate
Committee on Finance.
After considering the findings from
the Report to Congress and
recommendations from MedPAC and
the Senate Committee on Finance, CMS,
along with our contractor, conducted
additional research on ways to improve
the payment accuracy under the current
payment system. Exploring all options
and different models ultimately led us
to further develop the Home Health
Groupings Model (HHGM). As
discussed in the CY 2018 HH PPS
proposed rule (82 FR 35294), we shared
5 Committee on Finance, United States Senate.
Staff Report on Home Health and the Medicare
Therapy Threshold. Washington, DC, 2011.
Accessed on March 28, 2017 at https://
www.finance.senate.gov/imo/media/doc/Home_
Health_Report_Final4.pdf.
6 Medicare Payment Advisory Commission
(MedPAC). ‘‘Home Health Services.’’ Report to
Congress: Medicare Payment Policy. Washington,
DC, March 2011. P. 182–183. Accessed on March
28, 2017 at https://www.medpac.gov/docs/defaultsource/reports/Mar11_Ch08.pdf?sfvrsn=0.
7 Medicare Payment Advisory Commission
(MedPAC). ‘‘Home Health Care Services.’’ Report to
Congress: Medicare Payment Policy. Washington,
DC, March 2017. P. 243–244. Accessed on March
28, 2017 at https://www.medpac.gov/docs/defaultsource/reports/mar17_medpac_ch9.pdf?sfvrsn=0.
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the analysis and development of the
HHGM with both internal and external
stakeholders via technical expert panels,
clinical workgroups, special open door
forums, in the CY 2016 HH PPS
proposed rule (80 FR 39840) and the CY
2017 HH PPS proposed rule (81 FR
43744), in a detailed technical report
posted on the CMS Web site in
December 2016 (followed by additional
technical and clinical expert panels)
and a National Provider Call in January
2017. The HHGM uses 30-day periods,
rather than 60-day episodes, and relies
more heavily on clinical characteristics
and other patient information (for
example, principal diagnosis, functional
level, comorbid conditions, admission
source, and timing) to place patients
into meaningful payment categories,
rather than the current therapy-driven
system, which are the major differences
between the current system and the
HHGM.
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III. Provisions of the Proposed Rule:
Payment Under the Home Health
Prospective Payment System (HH PPS)
and Responses to Comments
In the July 28, 2017 Federal Register
(82 FR 35270 through 35393), we
published the proposed rule titled
‘‘Medicare and Medicaid Programs; CY
2018 Home Health Prospective Payment
System Rate Update and Proposed CY
2019 Case-Mix Adjustment
Methodology Refinements; Home Health
Value-Based Purchasing Model; and
Home Health Quality Reporting
Requirements’’. We received
approximately 1,346 timely comments
from the public, including comments
from home health agencies, national and
state provider associations, patient and
other advocacy organizations, nurses,
and physical therapists. In the following
sections, we summarize the proposed
provisions and the public comments,
and provide the responses to comments.
A. Monitoring for Potential Impacts—
Affordable Care Act Rebasing
Adjustments
In the CY 2018 HH PPS proposed rule
(82 FR 35277), we provided a summary
of analysis on fiscal year (FY) 2015 HHA
cost report data and how such data, if
used, would impact our estimate of the
percentage difference between Medicare
payments and HHA costs used to
calculate the Affordable Care Act
rebasing adjustments. In addition, we
presented information on Medicare
home health utilization statistics and
trends that included HHA claims data
through CY 2016. We will continue
monitoring the impacts due to the
rebasing adjustments and other policy
changes and will provide the industry
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with periodic updates on our analysis in
rulemaking and announcements on the
HHA Center Web page at https://
www.cms.gov/Center/Provider-Type/
Home-Health-Agency-HHA-Center.html.
The following is a summary of the
comments received on the analysis of
HHA cost report and utilization data
and our responses.
Comment: A commenter noted that it
may come as no surprise that payments
exceed costs by 21 percent, given that
Medicare payment for home health is
statutorily required to be based on a
prospective payment system and the
industry is now 90 percent for-profit,
with incentives to admit only the most
profitable cases. The commenter went
on to state that home health payments
from Medicare Advantage (MA) plans
are inadequate and that HHAs subsidize
low payments from MA plans with
payments for fee-for-service patients.
The commenter further noted that the
number of patients coming into home
health care from the community (rather
than following an acute or post-acute
care stay) has risen in response to
deliberate Medicare and public health
effort to keep patients out of the
hospital. Similar comments from
MedPAC stated that CMS’s review of
utilization is consistent with the
Commission’s findings on access to
care, and the analysis of the cost and
utilization data in the proposed rule
underscores the Commission’s longstanding concern that the Patient
Protection and Affordable Care Act
(PPACA) rebasing provision would not
adequately reduce payments.
Response: We thank the commenters
for their feedback on the HHA cost and
utilization data presented in the
proposed rule. We will continue
monitoring the impacts due to the
rebasing adjustments and other policy
changes and will provide the industry
with periodic updates on our analysis in
rulemaking or announcements on the
HHA Center Web page at: https://
www.cms.gov/Center/Provider-Type/
Home-Health-Agency-HHA-Center.html.
Comment: A commenter questioned
whether CMS did any trimming to the
cost report data used to populate Table
2 in the CY 2018 HH PPS proposed rule
and whether NRS costs were excluded
from this calculation.
Response: As we noted in the CY
2018 HH PPS proposed rule (82 FR
35277), to determine the 2015 average
cost per visit per discipline, we applied
the same trimming methodology
outlined in the CY 2014 HH PPS
proposed rule (78 FR 40284) and
weighted the costs per visit from the
2015 cost reports by size, facility type,
and urban/rural location so the costs per
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51683
visit were nationally representative
according to 2015 claims data. The 2015
average number of visits was taken from
2015 claims data (82 FR 35277). Because
CMS currently pays for NRS using a
separate conversion factor, NRS costs
were not included in Table 2 as the
national, standardized 60-day episode
payment amount only reflects the cost
of care related to skilled nursing,
physical therapy, occupational therapy,
speech-language pathology, home health
aide, and medical social services. The
payment for NRS is calculated through
the NRS conversion factor, multiplied
by the weights for the six severity levels.
B. CY 2018 HH PPS Case-Mix Weights
In the CY 2015 HH PPS final rule (79
FR 66072), we finalized a policy to
annually recalibrate the HH PPS casemix weights—adjusting the weights
relative to one another—using the most
current, complete data available. To
recalibrate the HH PPS case-mix weights
for CY 2018, we will use the same
methodology finalized in the CY 2008
HH PPS final rule (72 FR 49762), the CY
2012 HH PPS final rule (76 FR 68526),
and the CY 2015 HH PPS final rule (79
FR 66032). Annual recalibration of the
HH PPS case-mix weights ensures that
the case-mix weights reflect, as
accurately as possible, current home
health resource use and changes in
utilization patterns.
To generate the CY 2018 HH PPS
case-mix weights, we used CY 2016
home health claims data (as of August
17, 2017) with linked OASIS data.
These data are the most current and
complete data available at this time. We
noted in the proposed rule that we
would use CY 2016 home health claims
data (as of June 30, 2017 or later) with
linked OASIS data to generate the CY
2018 HH PPS case-mix weights for this
final rule. The process we used to
calculate the HH PPS case-mix weights
is outlined in this section.
Step 1: Re-estimate the four-equation
model to determine the clinical and
functional points for an episode using
wage-weighted minutes of care as our
dependent variable for resource use.
The wage-weighted minutes of care are
determined using the CY 2015 Bureau of
Labor Statistics national hourly wage
plus fringe rates for the six home health
disciplines and the minutes per visit
from the claim. The points for each of
the variables for each leg of the model,
updated with CY 2016 home health
claims data, are shown in Table 2. The
points for the clinical variables are
added together to determine an
episode’s clinical score. The points for
the functional variables are added
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together to determine an episode’s
functional score.
TABLE 2—CASE-MIX ADJUSTMENT VARIABLES AND SCORES
Episode number within sequence of adjacent episodes ....................................
Therapy visits ......................................................................................................
EQUATION: ........................................................................................................
1 or 2
0–13
1
1 or 2
14+
2
3+
0–13
3
3+
14+
4
........................
........................
........................
........................
1
2
........................
1
4
3
........................
16
........................
........................
........................
........................
........................
1
........................
........................
4
........................
........................
10
1
5
........................
9
........................
........................
........................
7
........................
........................
2
........................
........................
........................
........................
........................
1
3
........................
3
9
4
........................
6
........................
2
9
4
2
4
2
4
3
........................
9
2
2
........................
4
........................
........................
........................
........................
........................
3
7
5
11
7
1
7
........................
3
........................
3
7
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
2
........................
........................
........................
1
........................
3
17
6
17
6
14
7
14
2
........................
........................
........................
2
2
........................
........................
........................
........................
3
4
4
9
4
7
2
........................
1
........................
4
........................
16
17
17
15
16
........................
........................
6
19
31
13
17
7
6
1
3
11
........................
8
........................
........................
5
........................
........................
2
4
7
10
8
9
6
5
........................
........................
2
........................
18
17
12
15
6
........................
........................
6
17
25
13
17
13
10
........................
2
8
........................
1
6
........................
........................
5
1
........................
6
........................
........................
2
........................
CLINICAL DIMENSION
1
2
3
4
5
6
.......................
.......................
.......................
.......................
.......................
.......................
7 .......................
8 .......................
9 .......................
10 .....................
11 .....................
12 .....................
13 .....................
14 .....................
15 .....................
16 .....................
17 .....................
18 .....................
19 .....................
20 .....................
21 .....................
22 .....................
23 .....................
24 .....................
25 .....................
26 .....................
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27 .....................
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
Primary or Other Diagnosis = Blindness/Low Vision .........................................
Primary or Other Diagnosis = Blood disorders ..................................................
Primary or Other Diagnosis = Cancer, selected benign neoplasms ..................
Primary Diagnosis = Diabetes ............................................................................
Other Diagnosis = Diabetes ...............................................................................
Primary or Other Diagnosis = Dysphagia AND Primary or Other Diagnosis =
Neuro 3—Stroke.
Primary or Other Diagnosis = Dysphagia AND M1030 (Therapy at home) = 3
(Enteral).
Primary or Other Diagnosis = Gastrointestinal disorders ...................................
Primary or Other Diagnosis = Gastrointestinal disorders AND M1630
(ostomy)= 1 or 2.
Primary or Other Diagnosis = Gastrointestinal disorders AND Primary or
Other Diagnosis = Neuro 1—Brain disorders and paralysis, OR Neuro 2—
Peripheral neurological disorders, OR Neuro 3—Stroke, OR Neuro 4—Multiple Sclerosis.
Primary or Other Diagnosis = Heart Disease OR Hypertension ........................
Primary Diagnosis = Neuro 1—Brain disorders and paralysis ...........................
Primary or Other Diagnosis = Neuro 1—Brain disorders and paralysis AND
M1840 (Toilet transfer) = 2 or more.
Primary or Other Diagnosis = Neuro 1—Brain disorders and paralysis OR
Neuro 2—Peripheral neurological disorders AND M1810 or M1820 (Dressing upper or lower body) = 1, 2, or 3.
Primary or Other Diagnosis = Neuro 3—Stroke .................................................
Primary or Other Diagnosis = Neuro 3—Stroke AND M1810 or M1820
(Dressing upper or lower body) = 1, 2, or 3.
Primary or Other Diagnosis = Neuro 3—Stroke AND M1860 (Ambulation) = 4
or more.
Primary or Other Diagnosis = Neuro 4—Multiple Sclerosis AND AT LEAST
ONE OF THE FOLLOWING: M1830 (Bathing) = 2 or more OR M1840 (Toilet transfer) = 2 or more OR M1850 (Transferring) = 2 or more OR M1860
(Ambulation) = 4 or more.
Primary or Other Diagnosis = Ortho 1—Leg Disorders or Gait Disorders AND
M1324 (most problematic pressure ulcer stage) = 1, 2, 3 or 4.
Primary or Other Diagnosis = Ortho 1—Leg OR Ortho 2—Other orthopedic
disorders AND M1030 (Therapy at home) = 1 (IV/Infusion) or 2 (Parenteral).
Primary or Other Diagnosis = Psych 1—Affective and other psychoses, depression.
Primary or Other Diagnosis = Psych 2—Degenerative and other organic psychiatric disorders.
Primary or Other Diagnosis = Pulmonary disorders ..........................................
Primary or Other Diagnosis = Pulmonary disorders AND M1860 (Ambulation)
= 1 or more.
Primary Diagnosis = Skin 1—Traumatic wounds, burns, and post-operative
complications.
Other Diagnosis = Skin 1—Traumatic wounds, burns, post-operative complications.
Primary or Other Diagnosis = Skin 1—Traumatic wounds, burns, and post-operative complications OR Skin 2—Ulcers and other skin conditions AND
M1030 (Therapy at home) = 1 (IV/Infusion) or 2 (Parenteral).
Primary or Other Diagnosis = Skin 2—Ulcers and other skin conditions ..........
Primary or Other Diagnosis = Tracheostomy .....................................................
Primary or Other Diagnosis = Urostomy/Cystostomy ........................................
M1030 (Therapy at home) = 1 (IV/Infusion) or 2 (Parenteral) ...........................
M1030 (Therapy at home) = 3 (Enteral) ............................................................
M1200 (Vision) = 1 or more ...............................................................................
M1242 (Pain)= 3 or 4 .........................................................................................
M1311 = Two or more pressure ulcers at stage 3 or 4 .....................................
M1324 (Most problematic pressure ulcer stage) = 1 or 2 ..................................
M1324 (Most problematic pressure ulcer stage)= 3 or 4 ...................................
M1334 (Stasis ulcer status) = 2 .........................................................................
M1334 (Stasis ulcer status) = 3 .........................................................................
M1342 (Surgical wound status) = 2 ...................................................................
M1342 (Surgical wound status) = 3 ...................................................................
M1400 (Dyspnea) = 2, 3, or 4 ............................................................................
M1620 (Bowel Incontinence) = 2 to 5 ................................................................
M1630 (Ostomy) = 1 or 2 ...................................................................................
M2030 (Injectable Drug Use) = 0, 1, 2, or 3 ......................................................
FUNCTIONAL DIMENSION
46 .....................
47 .....................
48 .....................
VerDate Sep<11>2014
M1810 or M1820 (Dressing upper or lower body) = 1, 2, or 3 ..........................
M1830 (Bathing) = 2 or more .............................................................................
M1840 (Toilet transferring) = 2 or more .............................................................
20:38 Nov 06, 2017
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07NOR2
51685
Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
TABLE 2—CASE-MIX ADJUSTMENT VARIABLES AND SCORES—Continued
49 .....................
50 .....................
51 .....................
M1850 (Transferring) = 2 or more ......................................................................
M1860 (Ambulation) = 1, 2 or 3 .........................................................................
M1860 (Ambulation) = 4 or more .......................................................................
3
7
8
1
........................
9
2
4
7
.
........................
7
Source: CY 2016 Medicare claims data for episodes ending on or before December 31, 2016 (as of August 17, 2017) for which we had a linked
OASIS assessment. LUPA episodes, outlier episodes, and episodes with PEP adjustments were excluded.
Note(s): Points are additive; however, points may not be given for the same line item in the table more than once. Please see Medicare Home
Health Diagnosis Coding guidance at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/HomeHealthPPS/coding_billing.html for
definitions of primary and secondary diagnoses.
In updating the four-equation model
for CY 2018, using 2016 home health
claims data (the last update to the fourequation model for CY 2017 used CY
2015 home health claims data), there
were few changes to the point values for
the variables in the four-equation
model. These relatively minor changes
reflect the change in the relationship
between the grouper variables and
resource use between CY 2015 and CY
2016. The CY 2018 four-equation model
resulted in 120 point-giving variables
being used in the model (as compared
to the 124 variables for the CY 2017
recalibration). There were 8 variables
that were added to the model and 12
variables that were dropped from the
model due to the absence of additional
resources associated with the variable.
Of the variables that were in both the
four-equation model for CY 2017 and
the four-equation model for CY 2018,
the points for 14 variables increased in
the CY 2018 four-equation model and
the points for 48 variables decreased in
the CY 2018 4-equation model. There
were 50 variables with the same point
values.
Step 2: Redefining the clinical and
functional thresholds so they are
reflective of the new points associated
with the CY 2018 four-equation model.
After estimating the points for each of
the variables and summing the clinical
and functional points for each episode,
we look at the distribution of the
clinical score and functional score,
breaking the episodes into different
steps. The categorizations for the steps
are as follows:
• Step 1: First and second episodes,
0–13 therapy visits.
• Step 2.1: First and second episodes,
14–19 therapy visits.
• Step 2.2: Third episodes and
beyond, 14–19 therapy visits.
• Step 3: Third episodes and beyond,
0–13 therapy visits.
• Step 4: Episodes with 20+ therapy
visits
Then, we divide the distribution of
the clinical score for episodes within a
step such that a third of episodes are
classified as low clinical score, a third
of episodes are classified as medium
clinical score, and a third of episodes
are classified as high clinical score. The
same approach is then done looking at
the functional score. It was not always
possible to evenly divide the episodes
within each step into thirds due to
many episodes being clustered around
one particular score.8 Also, we looked at
the average resource use associated with
each clinical and functional score and
used that as a guide for setting our
thresholds. We grouped scores with
similar average resource use within the
same level (even if it meant that more
or less than a third of episodes were
placed within a level). The new
thresholds, based off the CY 2018 fourequation model points are shown in
Table 3.
TABLE 3—CY 2018 CLINICAL AND FUNCTIONAL THRESHOLDS
1st and 2nd episodes
0 to 13
therapy visits
3rd+ episodes
14 to 19
therapy visits
0 to 13
therapy visits
All episodes
14 to 19
therapy visits
20+ therapy
visits
Grouping Step
1
2 .......................
3 .......................
4 .......................
5
Equations used to calculate points (see Table 1)
1
2 .......................
3 .......................
4 .......................
(2&4)
0 to 1 ................
2 to 3 ................
4+ .....................
0 to 13 ..............
14 .....................
15+ ...................
0 to 1 ................
2 to 7 ................
8+ .....................
0 to 7 ................
8 to 15 ..............
16+ ...................
0 to 1 ................
2 .......................
3+ .....................
0 to 6 ................
7 to 10 ..............
11+ ...................
0 to 1 ................
2 to 9 ................
10+ ...................
0 to 2 ................
3 to 7 ................
8+ .....................
0 to
4 to
17+
0 to
3 to
7+
Dimension
Severity
Level
Clinical .............................................
asabaliauskas on DSKBBXCHB2PROD with RULES
Functional ........................................
C1
C2
C3
F1
F2
F3
............
............
............
............
............
............
3
16
2
6
Step 3: Once the clinical and
functional thresholds are determined
and each episode is assigned a clinical
and functional level, the payment
regression is estimated with an
episode’s wage-weighted minutes of
care as the dependent variable.
Independent variables in the model are
indicators for the step of the episode as
well as the clinical and functional levels
within each step of the episode. Like the
four-equation model, the payment
regression model is also estimated with
robust standard errors that are clustered
at the beneficiary level. Table 4 shows
the regression coefficients for the
variables in the payment regression
model updated with CY 2016 home
health claims data. The R-squared value
for the payment regression model is
8 For Step 1, 45.3 percent of episodes were in the
medium functional level (All with score 14).
For Step 2.1, 87.3 percent of episodes were in the
low functional level (Most with scores 5 to 7).
For Step 2.2, 81.9 percent of episodes were in the
low functional level (Most with score 2).
For Step 3, 46.3 percent of episodes were in the
medium functional level (Most with score 10).
For Step 4, 48.7 percent of episodes were in the
medium functional level (Most with score 5 or 6).
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E:\FR\FM\07NOR2.SGM
07NOR2
51686
Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
0.5095 (an increase from 0.4919 for the
CY 2017 recalibration).
TABLE 4—PAYMENT REGRESSION MODEL
Payment regression
from 4-equation
model for CY 2018
Step 1, Clinical Score Medium ....................................................................................................................................................
Step 1, Clinical Score High .........................................................................................................................................................
Step 1, Functional Score Medium ...............................................................................................................................................
Step 1, Functional Score High ....................................................................................................................................................
Step 2.1, Clinical Score Medium .................................................................................................................................................
Step 2.1, Clinical Score High ......................................................................................................................................................
Step 2.1, Functional Score Medium ............................................................................................................................................
Step 2.1, Functional Score High .................................................................................................................................................
Step 2.2, Clinical Score Medium .................................................................................................................................................
Step 2.2, Clinical Score High ......................................................................................................................................................
Step 2.2, Functional Score Medium ............................................................................................................................................
Step 2.2, Functional Score High .................................................................................................................................................
Step 3, Clinical Score Medium ....................................................................................................................................................
Step 3, Clinical Score High .........................................................................................................................................................
Step 3, Functional Score Medium ...............................................................................................................................................
Step 3, Functional Score High ....................................................................................................................................................
Step 4, Clinical Score Medium ....................................................................................................................................................
Step 4, Clinical Score High .........................................................................................................................................................
Step 4, Functional Score Medium ...............................................................................................................................................
Step 4, Functional Score High ....................................................................................................................................................
Step 2.1, 1st and 2nd Episodes, 14 to 19 Therapy Visits ..........................................................................................................
Step 2.2, 3rd+ Episodes, 14 to 19 Therapy Visits ......................................................................................................................
Step 3, 3rd+ Episodes, 0–13 Therapy Visits ..............................................................................................................................
Step 4, All Episodes, 20+ Therapy Visits ....................................................................................................................................
Intercept .......................................................................................................................................................................................
$24.58
54.24
72.76
107.48
48.81
135.99
31.51
57.73
39.37
194.18
21.53
56.25
17.07
95.93
59.15
90.40
80.09
263.75
27.97
62.20
512.27
523.60
¥72.22
907.99
389.35
Source: CY 2016 Medicare claims data for episodes ending on or before December 31, 2016 (as of August 17, 2017) for which we had a
linked OASIS assessment.
asabaliauskas on DSKBBXCHB2PROD with RULES
Step 4: We use the coefficients from
the payment regression model to predict
each episode’s wage-weighted minutes
of care (resource use). We then divide
these predicted values by the mean of
the dependent variable (that is, the
average wage-weighted minutes of care
across all episodes used in the payment
regression). This division constructs the
weight for each episode, which is
simply the ratio of the episode’s
predicted wage-weighted minutes of
care divided by the average wageweighted minutes of care in the sample.
Each episode is then aggregated into one
of the 153 home health resource groups
(HHRGs) and the ‘‘raw’’ weight for each
HHRG was calculated as the average of
the episode weights within the HHRG.
Step 5: The raw weights associated
with 0 to 5 therapy visits are then
increased by 3.75 percent, the weights
associated with 14 to 15 therapy visits
are decreased by 2.5 percent, and the
weights associated with 20+ therapy
visits are decreased by 5 percent. These
adjustments to the case-mix weights
were finalized in the CY 2012 HH PPS
final rule (76 FR 68557) and were done
to address MedPAC’s concerns that the
HH PPS overvalues therapy episodes
and undervalues non-therapy episodes
and to better align the case-mix weights
with episode costs estimated from cost
report data.9
Step 6: After the adjustments in Step
5 are applied to the raw weights, the
weights are further adjusted to create an
increase in the payment weights for the
therapy visit steps between the therapy
thresholds. Weights with the same
clinical severity level, functional
severity level, and early/later episode
status were grouped together. Then
within those groups, the weights for
each therapy step between thresholds
9 Medicare Payment Advisory Commission
(MedPAC), Report to the Congress: Medicare
Payment Policy. March 2011, p. 176.
10 When computing the average, we compute a
weighted average, assigning a value of one to each
normal episode and a value equal to the episode
length divided by 60 for PEPs.
VerDate Sep<11>2014
20:38 Nov 06, 2017
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are gradually increased. We do this by
interpolating between the main
thresholds on the model (from 0 to 5 to
14 to 15 therapy visits, and from 14 to
15 to 20+ therapy visits). We use a
linear model to implement the
interpolation so the payment weight
increase for each step between the
thresholds (such as the increase
between 0 and 5 therapy visits and 6
therapy visits and the increase between
6 therapy visits and 7 to 9 therapy
visits) are constant. This interpolation is
identical to the process finalized in the
CY 2012 HH PPS final rule (76 FR
68555).
Step 7: The interpolated weights are
then adjusted so that the average casemix for the weights is equal to 1.0000.10
This last step creates the final CY 2018
case-mix weights shown in Table 5.
E:\FR\FM\07NOR2.SGM
07NOR2
Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
51687
TABLE 5—CY 2018 CASE-MIX PAYMENT WEIGHTS
asabaliauskas on DSKBBXCHB2PROD with RULES
Pay group
10111
10112
10113
10114
10115
10121
10122
10123
10124
10125
10131
10132
10133
10134
10135
10211
10212
10213
10214
10215
10221
10222
10223
10224
10225
10231
10232
10233
10234
10235
10311
10312
10313
10314
10315
10321
10322
10323
10324
10325
10331
10332
10333
10334
10335
21111
21112
21113
21121
21122
21123
21131
21132
21133
21211
21212
21213
21221
21222
21223
21231
21232
21233
21311
21312
21313
21321
21322
Description
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
VerDate Sep<11>2014
Clinical and
functional
levels
(1 = Low;
2 = Medium;
3 = High)
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
1st
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
and
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
2nd
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
Episodes,
20:38 Nov 06, 2017
Jkt 244001
0 to 5 Therapy Visits ...........................................................................
6 Therapy Visits ..................................................................................
7 to 9 Therapy Visits ...........................................................................
10 Therapy Visits ................................................................................
11 to 13 Therapy Visits .......................................................................
0 to 5 Therapy Visits ...........................................................................
6 Therapy Visits ..................................................................................
7 to 9 Therapy Visits ...........................................................................
10 Therapy Visits ................................................................................
11 to 13 Therapy Visits .......................................................................
0 to 5 Therapy Visits ...........................................................................
6 Therapy Visits ..................................................................................
7 to 9 Therapy Visits ...........................................................................
10 Therapy Visits ................................................................................
11 to 13 Therapy Visits .......................................................................
0 to 5 Therapy Visits ...........................................................................
6 Therapy Visits ..................................................................................
7 to 9 Therapy Visits ...........................................................................
10 Therapy Visits ................................................................................
11 to 13 Therapy Visits .......................................................................
0 to 5 Therapy Visits ...........................................................................
6 Therapy Visits ..................................................................................
7 to 9 Therapy Visits ...........................................................................
10 Therapy Visits ................................................................................
11 to 13 Therapy Visits .......................................................................
0 to 5 Therapy Visits ...........................................................................
6 Therapy Visits ..................................................................................
7 to 9 Therapy Visits ...........................................................................
10 Therapy Visits ................................................................................
11 to 13 Therapy Visits .......................................................................
0 to 5 Therapy Visits ...........................................................................
6 Therapy Visits ..................................................................................
7 to 9 Therapy Visits ...........................................................................
10 Therapy Visits ................................................................................
11 to 13 Therapy Visits .......................................................................
0 to 5 Therapy Visits ...........................................................................
6 Therapy Visits ..................................................................................
7 to 9 Therapy Visits ...........................................................................
10 Therapy Visits ................................................................................
11 to 13 Therapy Visits .......................................................................
0 to 5 Therapy Visits ...........................................................................
6 Therapy Visits ..................................................................................
7 to 9 Therapy Visits ...........................................................................
10 Therapy Visits ................................................................................
11 to 13 Therapy Visits .......................................................................
14 to 15 Therapy Visits .......................................................................
16 to 17 Therapy Visits .......................................................................
18 to 19 Therapy Visits .......................................................................
14 to 15 Therapy Visits .......................................................................
16 to 17 Therapy Visits .......................................................................
18 to 19 Therapy Visits .......................................................................
14 to 15 Therapy Visits .......................................................................
16 to 17 Therapy Visits .......................................................................
18 to 19 Therapy Visits .......................................................................
14 to 15 Therapy Visits .......................................................................
16 to 17 Therapy Visits .......................................................................
18 to 19 Therapy Visits .......................................................................
14 to 15 Therapy Visits .......................................................................
16 to 17 Therapy Visits .......................................................................
18 to 19 Therapy Visits .......................................................................
14 to 15 Therapy Visits .......................................................................
16 to 17 Therapy Visits .......................................................................
18 to 19 Therapy Visits .......................................................................
14 to 15 Therapy Visits .......................................................................
16 to 17 Therapy Visits .......................................................................
18 to 19 Therapy Visits .......................................................................
14 to 15 Therapy Visits .......................................................................
16 to 17 Therapy Visits .......................................................................
PO 00000
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E:\FR\FM\07NOR2.SGM
C1F1S1
C1F1S2
C1F1S3
C1F1S4
C1F1S5
C1F2S1
C1F2S2
C1F2S3
C1F2S4
C1F2S5
C1F3S1
C1F3S2
C1F3S3
C1F3S4
C1F3S5
C2F1S1
C2F1S2
C2F1S3
C2F1S4
C2F1S5
C2F2S1
C2F2S2
C2F2S3
C2F2S4
C2F2S5
C2F3S1
C2F3S2
C2F3S3
C2F3S4
C2F3S5
C3F1S1
C3F1S2
C3F1S3
C3F1S4
C3F1S5
C3F2S1
C3F2S2
C3F2S3
C3F2S4
C3F2S5
C3F3S1
C3F3S2
C3F3S3
C3F3S4
C3F3S5
C1F1S1
C1F1S2
C1F1S3
C1F2S1
C1F2S2
C1F2S3
C1F3S1
C1F3S2
C1F3S3
C2F1S1
C2F1S2
C2F1S3
C2F2S1
C2F2S2
C2F2S3
C2F3S1
C2F3S2
C2F3S3
C3F1S1
C3F1S2
C3F1S3
C3F2S1
C3F2S2
07NOR2
CY 2018
weight
0.5595
0.6911
0.8227
0.9543
1.0859
0.6640
0.7832
0.9025
1.0217
1.1409
0.7139
0.8302
0.9466
1.0629
1.1792
0.5948
0.7325
0.8703
1.0080
1.1457
0.6994
0.8247
0.9500
1.0753
1.2007
0.7493
0.8717
0.9941
1.1166
1.2390
0.6374
0.7902
0.9429
1.0957
1.2484
0.7420
0.8823
1.0227
1.1630
1.3034
0.7919
0.9293
1.0668
1.2042
1.3417
1.2176
1.3807
1.5439
1.2601
1.4213
1.5826
1.2955
1.4600
1.6244
1.2835
1.4598
1.6361
1.3260
1.5004
1.6748
1.3614
1.5390
1.7166
1.4012
1.6188
1.8364
1.4437
1.6594
51688
Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
TABLE 5—CY 2018 CASE-MIX PAYMENT WEIGHTS—Continued
asabaliauskas on DSKBBXCHB2PROD with RULES
Pay group
21323
21331
21332
21333
22111
22112
22113
22121
22122
22123
22131
22132
22133
22211
22212
22213
22221
22222
22223
22231
22232
22233
22311
22312
22313
22321
22322
22323
22331
22332
22333
30111
30112
30113
30114
30115
30121
30122
30123
30124
30125
30131
30132
30133
30134
30135
30211
30212
30213
30214
30215
30221
30222
30223
30224
30225
30231
30232
30233
30234
30235
30311
30312
30313
30314
30315
30321
30322
Description
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
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................
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................
................
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................
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................
................
................
................
................
................
................
................
................
................
VerDate Sep<11>2014
Clinical and
functional
levels
(1 = Low;
2 = Medium;
3 = High)
1st and 2nd Episodes, 18 to 19 Therapy Visits .......................................................................
1st and 2nd Episodes, 14 to 15 Therapy Visits .......................................................................
1st and 2nd Episodes, 16 to 17 Therapy Visits .......................................................................
1st and 2nd Episodes, 18 to 19 Therapy Visits .......................................................................
3rd+ Episodes, 14 to 15 Therapy Visits ..................................................................................
3rd+ Episodes, 16 to 17 Therapy Visits ..................................................................................
3rd+ Episodes, 18 to 19 Therapy Visits ..................................................................................
3rd+ Episodes, 14 to 15 Therapy Visits ..................................................................................
3rd+ Episodes, 16 to 17 Therapy Visits ..................................................................................
3rd+ Episodes, 18 to 19 Therapy Visits ..................................................................................
3rd+ Episodes, 14 to 15 Therapy Visits ..................................................................................
3rd+ Episodes, 16 to 17 Therapy Visits ..................................................................................
3rd+ Episodes, 18 to 19 Therapy Visits ..................................................................................
3rd++ Episodes, 14 to 15 Therapy Visits ................................................................................
3rd+ Episodes, 16 to 17 Therapy Visits ..................................................................................
3rd+ Episodes, 18 to 19 Therapy Visits ..................................................................................
3rd+ Episodes, 14 to 15 Therapy Visits ..................................................................................
3rd+ Episodes, 16 to 17 Therapy Visits ..................................................................................
3rd+ Episodes, 18 to 19 Therapy Visits ..................................................................................
3rd+ Episodes, 14 to 15 Therapy Visits ..................................................................................
3rd+ Episodes, 16 to 17 Therapy Visits ..................................................................................
3rd+ Episodes, 18 to 19 Therapy Visits ..................................................................................
3rd+ Episodes, 14 to 15 Therapy Visits ..................................................................................
3rd+ Episodes, 16 to 17 Therapy Visits ..................................................................................
3rd+ Episodes, 18 to 19 Therapy Visits ..................................................................................
3rd+ Episodes, 14 to 15 Therapy Visits ..................................................................................
3rd+ Episodes, 16 to 17 Therapy Visits ..................................................................................
3rd+ Episodes, 18 to 19 Therapy Visits ..................................................................................
3rd+ Episodes, 14 to 15 Therapy Visits ..................................................................................
3rd+ Episodes, 16 to 17 Therapy Visits ..................................................................................
3rd+ Episodes, 18 to 19 Therapy Visits ..................................................................................
3rd+ Episodes, 0 to 5 Therapy Visits ......................................................................................
3rd+ Episodes, 6 Therapy Visits ..............................................................................................
3rd+ Episodes, 7 to 9 Therapy Visits ......................................................................................
3rd+ Episodes, 10 Therapy Visits ............................................................................................
3rd+ Episodes, 11 to 13 Therapy Visits ..................................................................................
3rd+ Episodes, 0 to 5 Therapy Visits ......................................................................................
3rd+ Episodes, 6 Therapy Visits ..............................................................................................
3rd+ Episodes, 7 to 9 Therapy Visits ......................................................................................
3rd+ Episodes, 10 Therapy Visits ............................................................................................
3rd+ Episodes, 11 to 13 Therapy Visits ..................................................................................
3rd+ Episodes, 0 to 5 Therapy Visits ......................................................................................
3rd+ Episodes, 6 Therapy Visits ..............................................................................................
3rd+ Episodes, 7 to 9 Therapy Visits ......................................................................................
3rd+ Episodes, 10 Therapy Visits ............................................................................................
3rd+ Episodes, 11 to 13 Therapy Visits ..................................................................................
3rd+ Episodes, 0 to 5 Therapy Visits ......................................................................................
3rd+ Episodes, 6 Therapy Visits ..............................................................................................
3rd+ Episodes, 7 to 9 Therapy Visits ......................................................................................
3rd+ Episodes, 10 Therapy Visits ............................................................................................
3rd+ Episodes, 11 to 13 Therapy Visits ..................................................................................
3rd+ Episodes, 0 to 5 Therapy Visits ......................................................................................
3rd+ Episodes, 6 Therapy Visits ..............................................................................................
3rd+ Episodes, 7 to 9 Therapy Visits ......................................................................................
3rd+ Episodes, 10 Therapy Visits ............................................................................................
3rd+ Episodes, 11 to 13 Therapy Visits ..................................................................................
3rd+ Episodes, 0 to 5 Therapy Visits ......................................................................................
3rd+ Episodes, 6 Therapy Visits ..............................................................................................
3rd+ Episodes, 7 to 9 Therapy Visits ......................................................................................
3rd+ Episodes, 10 Therapy Visits ............................................................................................
3rd+ Episodes, 11 to 13 Therapy Visits ..................................................................................
3rd+ Episodes, 0 to 5 Therapy Visits ......................................................................................
3rd+ Episodes, 6 Therapy Visits ..............................................................................................
3rd+ Episodes, 7 to 9 Therapy Visits ......................................................................................
3rd+ Episodes, 10 Therapy Visits ............................................................................................
3rd+ Episodes, 11 to 13 Therapy Visits ..................................................................................
3rd+ Episodes, 0 to 5 Therapy Visits ......................................................................................
3rd+ Episodes, 6 Therapy Visits ..............................................................................................
20:38 Nov 06, 2017
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07NOR2
CY 2018
weight
1.8751
1.4791
1.6981
1.9170
1.2328
1.3909
1.5489
1.2619
1.4225
1.5832
1.3088
1.4688
1.6288
1.2860
1.4615
1.6369
1.3151
1.4931
1.6712
1.3620
1.5394
1.7168
1.4951
1.6814
1.8677
1.5241
1.7130
1.9019
1.5710
1.7593
1.9476
0.4557
0.6111
0.7666
0.9220
1.0774
0.5407
0.6850
0.8292
0.9734
1.1177
0.5856
0.7303
0.8749
1.0195
1.1642
0.4802
0.6414
0.8025
0.9637
1.1249
0.5652
0.7152
0.8652
1.0151
1.1651
0.6101
0.7605
0.9109
1.0612
1.2116
0.5936
0.7739
0.9542
1.1345
1.3148
0.6786
0.8477
Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
51689
TABLE 5—CY 2018 CASE-MIX PAYMENT WEIGHTS—Continued
Pay group
asabaliauskas on DSKBBXCHB2PROD with RULES
30323
30324
30325
30331
30332
30333
30334
30335
40111
40121
40131
40211
40221
40231
40311
40321
40331
Description
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
................
3rd+ Episodes, 7 to 9 Therapy Visits ......................................................................................
3rd+ Episodes, 10 Therapy Visits ............................................................................................
3rd+ Episodes, 11 to 13 Therapy Visits ..................................................................................
3rd+ Episodes, 0 to 5 Therapy Visits ......................................................................................
3rd+ Episodes, 6 Therapy Visits ..............................................................................................
3rd+ Episodes, 7 to 9 Therapy Visits ......................................................................................
3rd+ Episodes, 10 Therapy Visits ............................................................................................
3rd+ Episodes, 11 to 13 Therapy Visits ..................................................................................
All Episodes, 20+ Therapy Visits .............................................................................................
All Episodes, 20+ Therapy Visits .............................................................................................
All Episodes, 20+ Therapy Visits .............................................................................................
All Episodes, 20+ Therapy Visits .............................................................................................
All Episodes, 20+ Therapy Visits .............................................................................................
All Episodes, 20+ Therapy Visits .............................................................................................
All Episodes, 20+ Therapy Visits .............................................................................................
All Episodes, 20+ Therapy Visits .............................................................................................
All Episodes, 20+ Therapy Visits .............................................................................................
To ensure the changes to the HH PPS
case-mix weights are implemented in a
budget neutral manner, we then apply a
case-mix budget neutrality factor to the
CY 2018 national, standardized 60-day
episode payment rate (see section
III.C.3. of this final rule). The case-mix
budget neutrality factor is calculated as
the ratio of total payments when the CY
2018 HH PPS case-mix weights
(developed using CY 2016 home health
claims data) are applied to CY 2016
utilization (claims) data to total
payments when CY 2017 HH PPS casemix weights (developed using CY 2015
home health claims data) are applied to
CY 2016 utilization data. This produces
a case-mix budget neutrality factor for
CY 2018 of 1.0160.
The following is a summary of the
comments and our responses to
comments on the CY 2018 case-mix
weights:
Comment: A few commenters stated
that CMS did not provide sufficient
transparency of the details and methods
used to recalibrate the HH PPS case-mix
weights in the proposed rule. In
addition, commenters stated that CMS
provided little justification for
recalibrating the case-mix weights just 1
year following the recalibration of casemix weights in CY 2017, 2 years since
the recalibration in 2016, and 5 years
since the recalibration for the CY 2012
HH PPS final rule. The commenters
noted that they opposed the
recalibration of the case weights for CY
2018, but supported the budget
neutrality adjustment to account for the
recalibrated case-mix weights if CMS
finalizes the recalibration.
VerDate Sep<11>2014
Clinical and
functional
levels
(1 = Low;
2 = Medium;
3 = High)
20:38 Nov 06, 2017
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Response: As stated in the CY 2018
HH PPS proposed rule (82 FR 35282),
the methodology used to recalibrate the
weights is identical to the methodology
used in the CY 2012 recalibration except
for the minor exceptions as noted in the
CY 2015 HH PPS proposed and final
rules (79 FR 38366 and 79 FR 66032,
respectively). In the CY 2015 HH PPS
final rule, we finalized annual
recalibration and the methodology to be
used for each year’s recalibration (79 FR
66072). For more detail, we also
encourage commenters to refer to the CY
2012 HH PPS proposed and final rules
(76 FR 40988 and 76 FR 68526,
respectively) and the November 1, 2011
‘‘Revision of the Case-Mix Weights for
the HH PPS Report’’ on our home page
at: https://www.cms.gov/center/
provider-Type/home-Health-AgencyHHA-Center.html for additional
information about the recalibration
methodology.
We note that in comparing the final
CY 2018 HH PPS case-mix weights (see
Table 5) to the final CY 2015 HH PPS
case-mix weights (79 FR 66062), the
case-mix weights change very little,
with most case-mix weights either
increasing or decreasing by 1 to 2
percent with no case-mix weights
increasing by more than 3 percent or
decreasing by more than 3 percent. The
aggregate decreases in the case-mix
weights are offset by the case-mix
budget neutrality factor, which is
applied to the national, standardized 60day episode payment rate. In other
words, although the case-mix weights
themselves may increase or decrease
from year-to-year, we correspondingly
offset any estimated increases or
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CY 2018
weight
1.0168
1.1859
1.3550
0.7235
0.8930
1.0625
1.2320
1.4015
1.7070
1.7438
1.7888
1.8124
1.8492
1.8942
2.0540
2.0908
2.1359
decreases in total payments under the
HH PPS, as a result of the case-mix
recalibration, by applying a budget
neutrality factor to the national,
standardized 60-day episode payment
rate. For CY 2018, the case-mix budget
neutrality factor will be 1.0160 as
described previously. The recalibration
of the case-mix weights is not intended
to increase or decrease overall HH PPS
payments, but rather is used to update
the relative differences in resource use
amongst the 153 groups in the HH PPS
case-mix system and maintain the level
of aggregate payments before
application of any other adjustments.
We will continue to monitor the
performance of any finalized case-mix
model, and will make changes to it as
necessary.
Final Decision: We are finalizing the
recalibrated scores for the case-mix
adjustment variables, clinical and
functional thresholds, payment
regression model, and case-mix weights
in Tables 2 through 5. For this final rule,
the CY 2018 scores for the case-mix
variables, the clinical and functional
thresholds, and the case-mix weights
were developed using complete CY
2016 claims data as of August 17, 2017.
We note that we finalized the
recalibration methodology and the
proposal to annually recalibrate the HH
PPS case-mix weights in the CY 2015
HH PPS final rule (79 FR 66072). No
additional proposals were made with
regard to the recalibration methodology
in the CY 2018 HH PPS proposed rule.
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Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
asabaliauskas on DSKBBXCHB2PROD with RULES
C. CY 2018 Home Health Payment Rate
Update
1. CY 2018 Home Health Market Basket
Update
Section 1895(b)(3)(B) of the Act
requires that the standard prospective
payment amounts for CY 2018 be
increased by a factor equal to the
applicable HH market basket update for
those HHAs that submit quality data as
required by the Secretary. The home
health market basket was rebased and
revised in CY 2013. A detailed
description of how we derive the HHA
market basket is available in the CY
2013 HH PPS final rule (77 FR 67080
through 67090).
Section 1895(b)(3)(B)(vi) of the Act,
requires that, in CY 2015 (and in
subsequent calendar years, except CY
2018 (under section 411(c) of the
Medicare Access and CHIP
Reauthorization Act of 2015 (MACRA)
(Pub. L. 114–10, enacted April 16,
2015)), the market basket percentage
under the HHA prospective payment
system as described in section
1895(b)(3)(B) of the Act be annually
adjusted by changes in economy-wide
productivity. Section
1886(b)(3)(B)(xi)(II) of the Act defines
the productivity adjustment to be equal
to the 10-year moving average of change
in annual economy-wide private
nonfarm business multifactor
productivity (MFP) (as projected by the
Secretary for the 10-year period ending
with the applicable fiscal year, calendar
year, cost reporting period, or other
annual period) (the ‘‘MFP adjustment’’).
The Bureau of Labor Statistics (BLS) is
the agency that publishes the official
measure of private nonfarm business
MFP. Please see https://www.bls.gov/mfp
to obtain the BLS historical published
MFP data.
Prior to the enactment of the MACRA,
which amended section 1895(b)(3)(B) of
the Act, the home health update
percentage for CY 2018 would have
been based on the estimated home
health market basket update of 2.5
percent (based on IHS Global Inc.’s
third-quarter 2017 forecast with
historical data through second-quarter
2017). Due to the requirements specified
at section 1895(b)(3)(B)(vi) of the Act
prior to the enactment of MACRA, the
estimated CY 2018 home health market
basket update of 2.5 percent would have
been reduced by a MFP adjustment as
mandated by the Affordable Care Act
(currently estimated to be 0.6 percentage
point for CY 2018). In effect, the home
health payment update percentage for
CY 2018 would have been 1.9 percent.
However, section 411(c) of the MACRA
amended section 1895(b)(3)(B) of the
VerDate Sep<11>2014
20:38 Nov 06, 2017
Jkt 244001
Act, such that, for home health
payments for CY 2018, the market
basket percentage increase is required to
be 1 percent.
Section 1895(b)(3)(B) of the Act
requires that the home health update be
decreased by 2 percentage points for
those HHAs that do not submit quality
data as required by the Secretary. For
HHAs that do not submit the required
quality data for CY 2018, the home
health payment update will be ¥1
percent (1 percent minus 2 percentage
points).
2. CY 2018 Home Health Wage Index
Sections 1895(b)(4)(A)(ii) and (b)(4)(C)
of the Act require the Secretary to
provide appropriate adjustments to the
proportion of the payment amount
under the HH PPS that account for area
wage differences, using adjustment
factors that reflect the relative level of
wages and wage-related costs applicable
to the furnishing of HH services. Since
the inception of the HH PPS, we have
used inpatient hospital wage data in
developing a wage index to be applied
to HH payments. We proposed to
continue this practice for CY 2018, as
we continue to believe that, in the
absence of HH-specific wage data, using
inpatient hospital wage data is
appropriate and reasonable for the HH
PPS. Specifically, we proposed to
continue to use the pre-floor, prereclassified hospital wage index as the
wage adjustment to the labor portion of
the HH PPS rates. For CY 2018, the
updated wage data are for hospital cost
reporting periods beginning on or after
October 1, 2013, and before October 1,
2014 (FY 2014 cost report data). We
apply the appropriate wage index value
to the labor portion of the HH PPS rates
based on the site of service for the
beneficiary (defined by section 1861(m)
of the Act as the beneficiary’s place of
residence).
To address those geographic areas in
which there are no inpatient hospitals,
and thus, no hospital wage data on
which to base the calculation of the CY
2018 HH PPS wage index, we proposed
to continue to use the same
methodology discussed in the CY 2007
HH PPS final rule (71 FR 65884) to
address those geographic areas in which
there are no inpatient hospitals. For
rural areas that do not have inpatient
hospitals, we proposed to use the
average wage index from all contiguous
Core Based Statistical Areas (CBSAs) as
a reasonable proxy. Currently, the only
rural area without a hospital from which
hospital wage data could be derived is
Puerto Rico. However, for rural Puerto
Rico, we do not apply this methodology
due to the distinct economic
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circumstances that exist there (for
example, due to the close proximity to
one another of almost all of Puerto
Rico’s various urban and non-urban
areas, this methodology would produce
a wage index for rural Puerto Rico that
is higher than that in half of its urban
areas). Instead, we proposed to continue
to use the most recent wage index
previously available for that area. For
urban areas without inpatient hospitals,
we use the average wage index of all
urban areas within the state as a
reasonable proxy for the wage index for
that CBSA. For CY 2018, the only urban
area without inpatient hospital wage
data is Hinesville, GA (CBSA 25980).
On February 28, 2013, OMB issued
Bulletin No. 13–01, announcing
revisions to the delineations of MSAs,
Micropolitan Statistical Areas, and
CBSAs, and guidance on uses of the
delineation of these areas. In the CY
2015 HH PPS final rule (79 FR 66085
through 66087), we adopted the OMB’s
new area delineations using a 1-year
transition. The most recent bulletin (No.
15–01) concerning the revised
delineations was published by the OMB
on July 15, 2015.
The CY 2018 wage index is available
on the CMS Web site at https://
www.cms.gov/Medicare/Medicare-Feefor-Service-Payment/HomeHealthPPS/
Home-Health-Prospective-PaymentSystem-Regulations-and-Notices.html.
3. CY 2018 Annual Payment Update
a. Background
The Medicare HH PPS has been in
effect since October 1, 2000. As set forth
in the July 3, 2000 final rule (65 FR
41128), the base unit of payment under
the Medicare HH PPS is a national,
standardized 60-day episode payment
rate. As set forth in § 484.220, we adjust
the national, standardized 60-day
episode payment rate by a case-mix
relative weight and a wage index value
based on the site of service for the
beneficiary.
To provide appropriate adjustments to
the proportion of the payment amount
under the HH PPS to account for area
wage differences, we apply the
appropriate wage index value to the
labor portion of the HH PPS rates. The
labor-related share of the case-mix
adjusted 60-day episode rate will
continue to be 78.535 percent and the
non-labor-related share will continue to
be 21.465 percent as set out in the CY
2013 HH PPS final rule (77 FR 67068).
The CY 2018 HH PPS rates use the same
case-mix methodology as set forth in the
CY 2008 HH PPS final rule with
comment period (72 FR 49762) and will
be adjusted as described in section III.B.
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Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
of this final rule. The following are the
steps we take to compute the case-mix
and wage-adjusted 60-day episode rate:
(1) Multiply the national 60-day
episode rate by the patient’s applicable
case-mix weight.
(2) Divide the case-mix adjusted
amount into a labor (78.535 percent)
and a non-labor portion (21.465
percent).
(3) Multiply the labor portion by the
applicable wage index based on the site
of service of the beneficiary.
(4) Add the wage-adjusted portion to
the non-labor portion, yielding the casemix and wage adjusted 60-day episode
rate, subject to any additional applicable
adjustments.
In accordance with section
1895(b)(3)(B) of the Act, we proposed
the annual update of the HH PPS rates.
Section 484.225 sets forth the specific
annual percentage update methodology.
In accordance with § 484.225(i), for a
HHA that does not submit HH quality
data, as specified by the Secretary, the
unadjusted national prospective 60-day
episode rate is equal to the rate for the
previous calendar year increased by the
applicable HH market basket index
amount minus 2 percentage points. Any
reduction of the percentage change will
apply only to the calendar year involved
and will not be considered in
computing the prospective payment
amount for a subsequent calendar year.
Medicare pays the national,
standardized 60-day case-mix and wageadjusted episode payment on a split
percentage payment approach. The split
percentage payment approach includes
an initial percentage payment and a
final percentage payment as set forth in
§ 484.205(b)(1) and (b)(2). We may base
the initial percentage payment on the
submission of a request for anticipated
payment (RAP) and the final percentage
payment on the submission of the claim
for the episode, as discussed in § 409.43.
The claim for the episode that the HHA
submits for the final percentage
payment determines the total payment
amount for the episode and whether we
make an applicable adjustment to the
60-day case-mix and wage-adjusted
episode payment. The end date of the
60-day episode as reported on the claim
determines which calendar year rates
Medicare will use to pay the claim.
We may also adjust the 60-day casemix and wage-adjusted episode
payment based on the information
submitted on the claim to reflect the
following:
• A low-utilization payment
adjustment (LUPA) is provided on a pervisit basis as set forth in §§ 484.205(c)
and 484.230.
• A partial episode payment (PEP)
adjustment as set forth in §§ 484.205(d)
and 484.235.
• An outlier payment as set forth in
§§ 484.205(e) and 484.240.
b. CY 2018 National, Standardized 60Day Episode Payment Rate
Section 1895(b)(3)(A)(i) of the Act
requires that the 60-day episode base
rate and other applicable amounts be
standardized in a manner that
eliminates the effects of variations in
relative case-mix and area wage
adjustments among different home
health agencies in a budget neutral
manner. To determine the CY 2018
national, standardized 60-day episode
payment rate, we apply a wage index
budget neutrality factor; a case-mix
budget neutrality factor described in
section III.B. of this final rule; a
reduction of 0.97 percent to account for
nominal case-mix growth from 2012 to
2014, as finalized in the CY 2016 HH
PPS final rule (80 FR 68646); and the
home health payment update percentage
51691
discussed in section III.C.1 of this final
rule.
To calculate the wage index budget
neutrality factor, we simulated total
payments for non-LUPA episodes using
the CY 2018 wage index and compared
it to our simulation of total payments for
non-LUPA episodes using the CY 2017
wage index. By dividing the total
payments for non-LUPA episodes using
the CY 2018 wage index by the total
payments for non-LUPA episodes using
the CY 2017 wage index, we obtain a
wage index budget neutrality factor of
1.0004. We will apply the wage index
budget neutrality factor of 1.0004 to the
calculation of the CY 2018 national,
standardized 60-day episode rate.
As discussed in section III.B. of the
proposed rule, to ensure the changes to
the case-mix weights are implemented
in a budget neutral manner, we
proposed to apply a case-mix weight
budget neutrality factor to the CY 2018
national, standardized 60-day episode
payment rate. The case-mix weight
budget neutrality factor is calculated as
the ratio of total payments when CY
2018 case-mix weights are applied to CY
2016 utilization (claims) data to total
payments when CY 2017 case-mix
weights are applied to CY 2016
utilization data. The case-mix budget
neutrality factor for CY 2018 is 1.0160
as described in section III.B of this final
rule.
Next, we apply a reduction of 0.97
percent to the national, standardized 60day payment rate for CY 2018 to
account for nominal case-mix growth
between CY 2012 and CY 2014. Lastly,
we will update the payment rates by the
CY 2018 home health payment update
percentage of 1 percent as mandated by
section 1895(b)(3)(B)(iii) of the Act. The
CY 2018 national, standardized 60-day
episode payment rate is calculated in
Table 6.
TABLE 6—CY 2018 60-DAY NATIONAL, STANDARDIZED 60-DAY EPISODE PAYMENT AMOUNT
Case-mix
weights
budget
neutrality
factor
Nominal
case-mix
growth
adjustment
(1–0.0097)
CY 2018 HH
payment
update
CY 2018
national,
standardized
60-day
episode
payment
$2,989.97 .............................................................................
asabaliauskas on DSKBBXCHB2PROD with RULES
CY 2017 national, standardized 60-day episode payment
Wage index
budget
neutrality
factor
× 1.0004
× 1.0160
× 0.9903
× 1.01
$3,039.64
The CY 2018 national, standardized
60-day episode payment rate for an
HHA that does not submit the required
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quality data is updated by the CY 2018
home health payment update of 1
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percent minus 2 percentage points and
is shown in Table 7.
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TABLE 7—CY 2017 NATIONAL, STANDARDIZED 60-DAY EPISODE PAYMENT AMOUNT FOR HHAS THAT DO NOT SUBMIT
THE QUALITY DATA
CY 2017 national, standardized 60-day episode payment
Wage index
budget neutrality
factor
Case-mix
weights
budget
neutrality
factor
Nominal
case-mix
growth
adjustment
(1–0.0097)
CY 2018 HH
payment
update
CY 2018
national,
standardized
60-day
episode
payment
$2,989.97 .............................................................................
× 1.0004
× 1.0160
× 0.9903
× 0.99
$2,979.45
c. CY 2018 National Per-Visit Rates
The national per-visit rates are used to
pay LUPAs (episodes with four or fewer
visits) and are also used to compute
imputed costs in outlier calculations.
The per-visit rates are paid by type of
visit or HH discipline. The six HH
disciplines are as follows:
• Home health aide (HH aide).
• Medical Social Services (MSS).
• Occupational therapy (OT).
• Physical therapy (PT).
• Skilled nursing (SN).
• Speech-language pathology (SLP).
To calculate the CY 2018 national pervisit rates, we started with the CY 2017
national per-visit rates. Then we applied
a wage index budget neutrality factor to
ensure budget neutrality for LUPA per-
visit payments. We calculated the wage
index budget neutrality factor by
simulating total payments for LUPA
episodes using the CY 2018 wage index
and comparing it to simulated total
payments for LUPA episodes using the
CY 2017 wage index. By dividing the
total payments for LUPA episodes using
the CY 2018 wage index by the total
payments for LUPA episodes using the
CY 2017 wage index, we obtained a
wage index budget neutrality factor of
1.0010. We apply the wage index budget
neutrality factor of 1.0010 in order to
calculate the CY 2018 national per-visit
rates.
The LUPA per-visit rates are not
calculated using case-mix weights.
Therefore, there is no case-mix weights
budget neutrality factor needed to
ensure budget neutrality for LUPA
payments. Lastly, the per-visit rates for
each discipline are updated by the CY
2018 home health payment update
percentage of 1 percent. The national
per-visit rates are adjusted by the wage
index based on the site of service of the
beneficiary. The per-visit payments for
LUPAs are separate from the LUPA addon payment amount, which is paid for
episodes that occur as the only episode
or initial episode in a sequence of
adjacent episodes. The CY 2018 national
per-visit rates are shown in Tables 8 and
9.
TABLE 8—CY 2018 NATIONAL PER-VISIT PAYMENT AMOUNTS FOR HHAS THAT DO SUBMIT THE REQUIRED QUALITY
DATA
CY 2017
per-visit
payment
HH Discipline
Home Health Aide ...........................................................................................
Medical Social Services ...................................................................................
Occupational Therapy ......................................................................................
Physical Therapy .............................................................................................
Skilled Nursing .................................................................................................
Speech-Language Pathology ..........................................................................
The CY 2018 per-visit payment rates
for HHAs that do not submit the
$64.23
227.36
156.11
155.05
141.84
168.52
required quality data are updated by the
CY 2018 HH payment update percentage
Wage index
budget
neutrality
factor
×
×
×
×
×
×
1.0010
1.0010
1.0010
1.0010
1.0010
1.0010
CY 2018
HH
payment
update
×
×
×
×
×
×
1.01
1.01
1.01
1.01
1.01
1.01
CY 2018
per-visit
payment
$64.94
229.86
157.83
156.76
143.40
170.38
of 1 percent minus 2 percentage points
and are shown in Table 9.
TABLE 9—CY 2018 NATIONAL PER-VISIT PAYMENT AMOUNTS FOR HHAS THAT DO NOT SUBMIT THE REQUIRED QUALITY
DATA
CY 2017
per-visit
rates
asabaliauskas on DSKBBXCHB2PROD with RULES
HH Discipline
Home Health Aide ...........................................................................................
Medical Social Services ...................................................................................
Occupational Therapy ......................................................................................
Physical Therapy .............................................................................................
Skilled Nursing .................................................................................................
Speech-Language Pathology ..........................................................................
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$64.23
227.36
156.11
155.05
141.84
168.52
Wage index
budget
neutrality
factor
×
×
×
×
×
×
1.0010
1.0010
1.0010
1.0010
1.0010
1.0010
E:\FR\FM\07NOR2.SGM
07NOR2
CY 2018
HH payment
update minus
2 percentage
points
×
×
×
×
×
×
0.99
0.99
0.99
0.99
0.99
0.99
CY 2018
per-visit
rates
$63.65
225.31
154.70
153.65
140.56
167.00
Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
d. Low-Utilization Payment Adjustment
(LUPA) Add-On Factors
LUPA episodes that occur as the only
episode or as an initial episode in a
sequence of adjacent episodes are
adjusted by applying an additional
amount to the LUPA payment before
adjusting for area wage differences. In
the CY 2014 HH PPS final rule (78 FR
72305), we changed the methodology for
calculating the LUPA add-on amount by
finalizing the use of three LUPA add-on
factors: 1.8451 for SN; 1.6700 for PT;
and 1.6266 for SLP. We multiply the
per-visit payment amount for the first
SN, PT, or SLP visit in LUPA episodes
that occur as the only episode or an
initial episode in a sequence of adjacent
episodes by the appropriate factor to
determine the LUPA add-on payment
amount. For example, in the case of
HHAs that do submit the required
quality data, for LUPA episodes that
occur as the only episode or an initial
51693
percent. We did not apply a
standardization factor as the NRS
payment amount calculated from the
conversion factor is not wage or casemix adjusted when the final claim
payment amount is computed. The NRS
conversion factor for CY 2018 is shown
in Table 10.
episode in a sequence of adjacent
episodes, if the first skilled visit is SN,
the payment for that visit will be
$264.59 (1.8451 multiplied by $143.40),
subject to area wage adjustment.
e. CY 2018 Non-Routine Medical
Supply (NRS) Payment Rates
All medical supplies (routine and
nonroutine) must be provided by the
HHA while the patient is under a home
health plan of care. Examples of
supplies that can be considered nonroutine include dressings for wound
care, I.V. supplies, ostomy supplies,
catheters, and catheter supplies.
Payments for NRS are computed by
multiplying the relative weight for a
particular severity level by the NRS
conversion factor. To determine the CY
2018 NRS conversion factor, we
updated the CY 2017 NRS conversion
factor ($52.50) by the CY 2018 home
health payment update percentage of 1
TABLE 10—CY 2018 NRS CONVERSION FACTOR FOR HHAS THAT DO
SUBMIT THE REQUIRED QUALITY
DATA
CY 2017
NRS
conversion
factor
CY 2018 HH
payment
update
CY 2018 NRS
conversion
factor
$52.50 .......
× 1.01
$53.03
Using the CY 2018 NRS conversion
factor, the payment amounts for the six
severity levels are shown in Table 11.
TABLE 11—CY 2018 NRS PAYMENT AMOUNTS FOR HHAS THAT DO SUBMIT THE REQUIRED QUALITY DATA
Points
(scoring)
Severity level
1
2
3
4
5
6
...................................................................................................................................................
...................................................................................................................................................
...................................................................................................................................................
...................................................................................................................................................
...................................................................................................................................................
...................................................................................................................................................
For HHAs that do not submit the
required quality data, we updated the
CY 2017 NRS conversion factor ($52.50)
by the CY 2018 home health payment
update percentage of 1 percent minus 2
percentage points. The CY 2018 NRS
conversion factor for HHAs that do not
submit quality data is shown in Table
12.
0 .....................
1 to 14 ...........
15 to 27 .........
28 to 48 .........
49 to 98 .........
99+ .................
Relative
weight
0.2698
0.9742
2.6712
3.9686
6.1198
10.5254
CY 2018 NRS
payment
amounts
$14.31
51.66
141.65
210.45
324.53
558.16
The payment amounts for the various
TABLE 12—CY 2018 NRS CONVERSION FACTOR FOR HHAS THAT DO severity levels based on the updated
NOT SUBMIT THE REQUIRED QUAL- conversion factor for HHAs that do not
submit quality data are calculated in
ITY DATA
Table 13.
CY 2017
NRS
conversion
factor
CY 2018 HH
payment
update
percentage
minus 2
percentage
points
CY 2018 NRS
conversion
factor
$52.50 .......
× 0.99
$51.98
TABLE 13—CY 2018 NRS PAYMENT AMOUNTS FOR HHAS THAT DO NOT SUBMIT THE REQUIRED QUALITY DATA
Points
(scoring)
asabaliauskas on DSKBBXCHB2PROD with RULES
Severity level
1
2
3
4
5
6
...................................................................................................................................................
...................................................................................................................................................
...................................................................................................................................................
...................................................................................................................................................
...................................................................................................................................................
...................................................................................................................................................
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0 .....................
1 to 14 ...........
15 to 27 .........
28 to 48 .........
49 to 98 .........
99+ .................
E:\FR\FM\07NOR2.SGM
07NOR2
Relative
weight
0.2698
0.9742
2.6712
3.9686
6.1198
10.5254
CY 2018 NRS
payment
amounts
$14.02
50.64
138.85
206.29
318.11
547.11
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asabaliauskas on DSKBBXCHB2PROD with RULES
f. Rural Add-On
Section 421(a) of the MMA required,
for HH services furnished in a rural area
(as defined in section 1886(d)(2)(D) of
the Act), for episodes or visits ending on
or after April 1, 2004, and before April
1, 2005, that the Secretary increase the
payment amount that otherwise would
have been made under section 1895 of
the Act for the services by 5 percent.
Section 5201 of the DRA amended
section 421(a) of the MMA. The
amended section 421(a) of the MMA
required, for HH services furnished in a
rural area (as defined in section
1886(d)(2)(D) of the Act), on or after
January 1, 2006, and before January 1,
2007, that the Secretary increase the
payment amount otherwise made under
section 1895 of the Act for those
services by 5 percent.
Section 3131(c) of the Affordable Care
Act amended section 421(a) of the MMA
to provide an increase of 3 percent of
the payment amount otherwise made
under section 1895 of the Act for HH
services furnished in a rural area (as
defined in section 1886(d)(2)(D) of the
Act), for episodes and visits ending on
or after April 1, 2010, and before
January 1, 2016.
Section 210 of the MACRA amended
section 421(a) of the MMA to extend the
rural add-on by providing an increase of
3 percent of the payment amount
otherwise made under section 1895 of
the Act for HH services provided in a
rural area (as defined in section
1886(d)(2)(D) of the Act), for episodes
and visits ending before January 1, 2018.
Therefore, for episodes and visits that
end on or after January 1, 2018, a rural
add-on payment will not apply.
The following is a summary of the
public comments received on the ‘‘CY
2018 Home Health Payment Rate
Update’’ proposals and our responses:
Comment: Several commenters stated
that they wanted CMS to rescind the
nominal case-mix reduction for CY
2018. Some commenters stated that
implementation of the nominal case-mix
reductions in 2016, 2017, and 2018
violated the limits on payment
reductions set out by the Congress, and
urged CMS to adhere to the statutory
limits on home health rate cuts.
Commenters expressed concerns with
the data and methodology used to
develop the proposed case-mix cuts and
stated that the annual recalibration may
have eliminated any practice of
assigning an inaccurate code to increase
reimbursement and questioned the
interaction between the rebasing
adjustments, nominal case-mix growth
reductions, and case-mix recalibration.
A few commenters stated that the
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baseline used in calculating the amount
of case-mix growth was inappropriate.
Some commenters noted that actual
program spending on home health was
consistently less than Congressional
Budget Office (CBO) estimates, and
questioned CMS’ authority to
implement case mix weight adjustments
when home health spending was less
than these estimates. Commenters stated
that there was no increase in aggregate
expenditures that warranted the
application of this statutory authority,
and CMS should withdraw its proposal.
Some commenters stated that CMS
should implement program integrity
measures to control aberrant coding by
some providers instead of imposing
across-the-board case mix creep
adjustments on all providers.
Response: We finalized the nominal
case-mix reduction for CY 2018 in the
CY 2016 HH PPS final rule. We did not
propose changes to the finalized
reduction for CY 2018, nor did we
propose any changes in the
methodology used to calculate nominal
case-mix growth in the CY 2018 HH PPS
proposed rule. The majority of the
comments received regarding the
payment reductions for nominal casemix growth were very similar to the
comments submitted during the
comment period for the CY 2016 HH
PPS proposed rule. Therefore, we
encourage commenters to review our
responses to the comments we received
on the payment reductions for nominal
case-mix growth in the CY 2016 HH PPS
final rule (80 FR 68639 through 68646),
which include responses on the
interaction between the rebasing and
recalibration of the case-mix weights on
the measurement of nominal case-mix
growth between 2012 and 2014, our
rationale for the methodology used to
determine ‘‘real’’ versus ‘‘nominal’’
case-mix growth in CYs 2012–2014, the
role of CBO estimates in our
determination of nominal case-mix
reductions, and our ability to target
nominal case-mix reductions to certain
providers rather the industry as a whole.
We will continue to monitor real and
nominal case-mix growth and may
propose additional reductions for
nominal case-mix growth, as needed, in
the future.
Comment: MedPAC stated that they
have long believed that it was necessary
for CMS to make adjustments to account
for nominal case-mix change to prevent
additional overpayments. MedPAC
stated that the CMS’ reduction to
account for nominal case-mix growth is
consistent with the agency’s past
findings on trends in case-mix change in
the payment system and thus is
warranted to ensure the accuracy of
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payments under the home health PPS.
MedPAC stated that a reduction of 0.97
percent should not significantly affect
access to care.
Response: We thank MedPAC for their
comments.
Comment: Several commenters stated
their belief that the CY 2018 payment
update of 1 percent is inadequate.
Response: We appreciate the
commenters’ concerns. However, the 1
percent payment update for CY 2018 is
mandated by section 1895(b)(3)(B)(iii) of
the Act, as amended by section 411(c)
of the MACRA.
Comment: Several commenters urged
CMS to continue providing rural add-on
payments in order that beneficiaries in
rural communities continue to have
access to home health services.
Response: The sunset of rural add-on
payments for CY 2018 is statutory and
we do not have the authority to reauthorize rural add-on payments for
episodes and visits ending on or after
January 1, 2018.11 However, we plan to
continue to monitor the costs associated
with providing home health care in
rural versus urban areas. We note that
in Chapter 9 of its 2013 Report to
Congress (available at https://
medpac.gov/docs/default-source/
reports/mar13_ch09.pdf?sfvrsn=0),
MedPAC stated that the use of the
‘‘broadly targeted add-on, providing the
same payment for all rural areas
regardless of access, results in rural
areas with the highest utilization
drawing a disproportionate share of the
add-on payments.’’ MedPAC stated that
‘‘70 percent of the episodes that
received the add-on payments in 2011
were in rural counties with utilization
significantly higher than the national
average’’ and recommended that
Medicare target payment adjustments
for rural areas to those areas that have
access challenges.
Comment: A commenter
recommended that CMS explore
policies that provide Medicare coverage
for services from therapy providers who
furnish telehealth services to their
patients as proper application of
telehealth rehabilitation therapy
services, particularly in underserved
areas, can potentially have a dramatic
impact on improving care, diminishing
negative consequences, and reducing
costs.
Response: The definition of a visit for
purposes of Medicare home health
services as set forth in § 409.48(c)
specifies that a visit is an episode of
personal contact with the beneficiary by
11 See U.S. CONST. art. I, § 9 (‘‘No money shall
be drawn from the Treasury, but in Consequence of
Appropriations made by Law’’).
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Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
staff of the HHA or others under
arrangements with the HHA for the
purpose of providing a covered service.
A telephone contact or telehealth visit
does not meet the definition of a visit
and therefore does not count as a visit.
While there is nothing to preclude an
HHA from furnishing services via
telehealth or other technologies that
they believe promote efficiencies, those
technologies are not specifically
recognized and paid by Medicare under
the home health benefit.
Comment: Several commenters
expressed concerns with the wage index
for rural areas in Maine, citing it as one
of the lowest in New England. Another
commenter questioned the validity of
the wage index data, especially in the
case of the CBSA for AlbanySchenectady-Troy, noting that in the
past 5 years, this CBSA has seen its
wage index reduced 5.41 percent, going
from 0.8647 in 2013 to a proposed CY
2018 wage index of 0.8179.
Response: As discussed in the CY
2017 HH PPS final rule (81 FR 76721),
we believe that the wage index values
are reflective of the labor costs in each
geographic area as they reflect the costs
included on the cost reports of hospitals
in those specific labor market areas. The
wage index values are based on data
submitted on the inpatient hospital cost
reports. We utilize efficient means to
ensure and review the accuracy of the
hospital cost report data and resulting
wage index. The home health wage
index is derived from the pre-floor, prereclassified wage index, which is
calculated based on cost report data
from hospitals paid under the Hospital
Inpatient Prospective Payment System
(IPPS). All IPPS hospitals must
complete the wage index survey
(Worksheet S–3, Parts II and III) as part
of their Medicare cost reports. Cost
reports will be rejected if Worksheet S–
3 is not completed. In addition,
Medicare contractors perform desk
reviews on all hospitals’ Worksheet S–
3 wage data, and we run edits on the
wage data to further ensure the accuracy
and validity of the wage data. We
believe that our review processes result
in an accurate reflection of the
applicable wages for the areas given.
The processes and procedures
describing how the inpatient hospital
wage index is developed are discussed
in the IPPS rule each year, with the
most recent discussion provided in the
FY 2018 IPPS final rule (82 FR 38130
through 38136 and 82 FR 38152 through
38156). Any provider type may submit
comments on the hospital wage index
during the annual IPPS rulemaking
cycle.
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Comment: A commenter stated that
CMS’s decision to switch from MSAs to
the CBSAs for the wage index
calculation has had serious financial
ramifications for New York HHAs. The
commenter stated that CMS’s shift to the
CBSA wage index designation has
resulted in below trend reimbursement
for New York City agencies.
Response: The MSA delineations as
well as the CBSA delineations are
determined by the OMB. The OMB
reviews its Metropolitan Area
definitions preceding each decennial
census to reflect recent population
changes. We believe that the OMB’s
CBSA designations reflect the most
recent available geographic
classifications and are a reasonable and
appropriate way to define geographic
areas for purposes of wage index values.
Comment: Several commenters
opposed the fact that hospitals are given
the opportunity to appeal their annual
wage index and apply for geographic
reclassification while HHAs in the same
geographic location are not given that
same privilege. The commenters believe
that this lack of parity between different
health care sectors further exemplifies
the inadequacy of CMS’s decision to
continue to use the pre-floor, prereclassified hospital wage index to
adjust home health services payment
rates. Another commenter suggests that
CMS include wage data from
reclassified hospitals in calculating
rural wage index values.
Response: We continue to believe that
the regulations and statutes that govern
the HH PPS do not provide a
mechanism for allowing HHAs to seek
geographic reclassification or to utilize
the rural floor provisions that exist for
IPPS hospitals. Section 4410(a) of the
BBA provides that the area wage index
applicable to any hospital that is located
in an urban area of a State may not be
less than the area wage index applicable
to hospitals located in rural areas in that
state. This is the rural floor provision
and it is specific to hospitals. The
reclassification provision at section
1886(d)(10)(C)(i) of the Act states that
the Board shall consider the application
of any subsection (d) hospital requesting
the Secretary change the hospital’s
geographic classification. This
reclassification provision is only
applicable to hospitals as defined in
section 1886(d) of the Act. In addition,
we do not believe that using hospital
reclassification data would be
appropriate as these data are specific to
the requesting hospitals and may or may
not apply to a given HHA.
We continue to believe that using the
pre-floor, pre-reclassified hospital wage
index as the wage adjustment to the
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51695
labor portion of the HH PPS rates is
appropriate and reasonable.
Comment: Several commenters
requested that CMS explore wholesale
revision and reform of the home health
wage index, including the development
of a home health-specific wage index.
Commenters noted that reform of the
home health wage index should address
the commenters’ following concerns and
opinions: (1) The impact on care access
and financial stability of HHAs at the
local level; (2) the unpredictable year-toyear swings in wage index values that
are often based on inaccurate or
incomplete hospital cost reports which
have negatively impacted HHAs
throughout the years and jeopardized
access to care; (3) the inadequacy and
inaccuracy of the pre-floor, prereclassified hospital wage index for
adjusting home health costs; and (4) the
labor market distortions created by
reclassification of hospitals in areas in
which home health labor costs are not
reclassified.
Response: We appreciate the
commenter’s recommendation to
continue exploring potential approaches
for wage index reform, including
collecting home health-specific wage
data in order to establish a home healthspecific wage index. We note that our
previous attempts at either proposing or
developing a home health-specific wage
index were not well-received by the
home health industry. In September 30,
1988 Federal Register notice (53 FR
38476), the Health Care Financing
Administration (HCFA), as CMS was
then known, implemented an HHAspecific wage index based on data
received from HHAs. Subsequently,
providers gave significant feedback
concerning the burden that the reporting
requirements posed and the accuracy of
the data. As a result, the Medicare
Catastrophic Coverage Act of 1988
retroactively repealed the use of an
HHA-specific wage index and
referenced use of the hospital wage
index (see section 1895(b)(4)(C) of the
Act). While this occurred many years
ago, we believe that HHAs would voice
similar concerns regarding the burden
such reporting requirements would
place on HHAs.
Consistent with our previous
responses to these recurring comments
(most recently published in the CY 2016
HH PPS final rule (80 FR 68654)), we
also note that developing such a wage
index would require a resourceintensive audit process similar to that
used for IPPS hospital data, to improve
the quality of the HHA cost report data
in order for it to be used as part of this
analysis. This audit process is quite
extensive in the case of approximately
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3,300 hospitals, it would be
significantly more so in the case of
approximately 11,000 HHAs. We believe
auditing all HHA cost reports, similar to
the process used to audit inpatient
hospital cost reports for purposes of the
IPPS wage index, would also place a
burden on providers in terms of
recordkeeping and completion of the
cost report worksheet.
We also believe that adopting such an
approach would require a significant
commitment of resources by CMS and
the Medicare Administrative
Contractors, potentially far in excess of
those required under the IPPS given that
there are more than three times as many
HHAs as there are hospitals. Therefore,
we continue to believe that, in the
absence of the appropriate home healthspecific wage data, using the pre-floor,
pre-reclassified inpatient hospital wage
data is appropriate and reasonable for
the HH PPS.
Finally, CMS has conducted research
on a possible alternative to the hospital
wage index. CMS issued its ‘‘Report to
Congress: Plan to Reform the Medicare
Wage Index’’ concerning the hospital
wage index, on April 11, 2012 and is
available on our Wage Index Reform
Web page https://www.cms.gov/
Medicare/Medicare-Fee-for-ServicePayment/AcuteInpatientPPS/WageIndex-Reform.html. This report
describes the concept of a commutingbased wage index (CBWI). However,
implementation of a CBWI may require
both statutory and regulatory changes.
In addition, we believe other
intermediate steps for implementation,
including the collection of commuting
data, may be necessary. In considering
alternative methodologies for area wage
adjustment, CMS would have to
consider whether the benefits of such
methodologies outweigh the reporting,
record keeping and audit burden that
would be placed on HHAs and/or other
providers.
Comment: Several commenters stated
that the pre-floor, pre-reclassified
hospital wage index is inadequate for
adjusting home health costs,
particularly in states like New York,
which has among the nation’s highest
labor costs, exacerbated, in the
commenters’ opinions, by their state’s
implementation of a phased-in $15 perhour minimum wage hike, which they
argue would be unfunded by Medicare.
The commenters estimated that the
minimum wage mandate, when fully
phased-in, would add $2 billion in costs
for that state’s HHAs across all payers
(Medicaid, Medicare, managed care,
commercial insurance and private-pay),
and would not be captured by the prefloor, pre-reclassified hospital wage
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index. One commenter recommended
that providers meeting higher minimum
wage standards, such as HHAs, obtain
additional supplemental funding to
better align payments with cost trends
impacting providers.
Response: Regarding minimum wage
standards, we note that such increases
will be reflected in future data used to
create the hospital wage index to the
extent that these changes to state
minimum wage standards are reflected
in increased wages to hospital staff.
Comment: Commenters raised issues
with CMS’s decision to maintain the
current policy of using the pre-floor,
pre-reclassified hospital wage index to
adjust home health services payment
rates because this resulted in volatility
in the home health wage index from one
year to the next. These commenters
believe that what they view as
unpredictable year-to-year swings in
wage index values were based on
inaccurate or incomplete hospital cost
reports.
Response: We appreciate the
commenters’ concerns regarding the
accuracy of the home health wage
index. We utilize efficient means to
ensure and review the accuracy of the
hospital cost report data and resulting
wage index. The home health wage
index is derived from the pre-floor, prereclassified wage index, which is
calculated based on cost report data
from hospitals paid under the IPPS. All
IPPS hospitals must complete the wage
index survey (Worksheet S–3, Parts II
and III) as part of their Medicare cost
reports. Cost reports will be rejected if
Worksheet S–3 is not completed. In
addition, Medicare contractors perform
desk reviews on all hospitals’
Worksheet S–3 wage data, and we run
edits on the wage data to further ensure
the accuracy and validity of the wage
data. We believe that our review
processes result in an accurate reflection
of the applicable wages for the areas
given. The processes and procedures
describing how the inpatient hospital
wage index is developed, including a
wage data verification and correction
process, are discussed in the IPPS rule
each year, with the most recent
discussion provided in the FY 2018
IPPS final rule (82 FR 38130 through
38136, and 82 FR 38152 through 38156).
Any provider type may submit
comments on the hospital wage index
during the annual IPPS rulemaking
cycle.
Comment: A commenter
recommended that CMS research the
impact of instituting a population
density adjustment to the labor portion
of the HH PPS payments.
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Response: As discussed in the CY
2017 HH PPS final rule (81 FR 76721),
we do not believe that a population
density adjustment is appropriate at this
time. Rural HHAs continually cite the
added cost of traveling from one patient
to the next patient. However, urban
HHAs cite the added costs associated
with needed security measures and
traffic congestion. The home health
wage index values in rural areas are not
necessarily lower than the home health
wage index values in urban areas. The
home health wage index reflects the
wages that inpatient hospitals pay in
their local geographic areas.
Final Decision: After considering the
comments received in response to the
CY 2018 HH PPS proposed rule, we are
finalizing our proposal to use the prefloor, pre-reclassified hospital inpatient
wage index as the wage adjustment to
the labor portion of the HH PPS rates.
For CY 2018, the updated wage data are
for the hospital cost reporting periods
beginning on or after October 1, 2013
and before October 1, 2014 (FY 2014
cost report data). In addition, we are
implementing the third and final year of
a 0.97 percent payment reduction to
account for nominal case-mix growth
from CY 2012 through CY 2014 when
finalizing the CY 2018 HH PPS payment
rates. We note that the payment
reductions to account for nominal casemix growth from 2012 to 2014 were
finalized in the CY 2016 HH PPS final
rule. No additional adjustments or
reductions were proposed in the CY
2018 proposed rule.
D. Payments for High-Cost Outliers
Under the HH PPS
1. Background
Section 1895(b)(5) of the Act allows
for the provision of an addition or
adjustment to the home health payment
amount in the case of outliers because
of unusual variations in the type or
amount of medically necessary care.
Outlier payments serve as a type of
‘‘reinsurance’’ whereby, under the HH
PPS, Medicare reimburses HHAs 80
percent of their costs for outlier cases
once the case exceeds an outlier
threshold amount. Prior to the
enactment of the Affordable Care Act,
section 1895(b)(5) of the Act stipulated
that projected total outlier payments
could not exceed 5 percent of total
projected or estimated HH payments in
a given year. In the July 3, 2000
Medicare Program; Prospective Payment
System for Home Health Agencies final
rule (65 FR 41188 through 41190), we
described the method for determining
outlier payments. Under this system,
outlier payments are made for episodes
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whose estimated costs exceed a
threshold amount for each Home Health
Resource Group (HHRG). The episode’s
estimated cost was established as the
sum of the national wage-adjusted pervisit payment amounts delivered during
the episode. The outlier threshold for
each case-mix group or Partial Episode
Payment (PEP) adjustment is defined as
the 60-day episode payment or PEP
adjustment for that group plus a fixeddollar loss (FDL) amount. The outlier
payment is defined to be a proportion of
the wage-adjusted estimated cost
beyond the wage-adjusted threshold.
The threshold amount is the sum of the
wage and case-mix adjusted PPS
episode amount and wage-adjusted FDL
amount. The proportion of additional
costs over the outlier threshold amount
paid as outlier payments is referred to
as the loss-sharing ratio.
In the CY 2010 HH PPS proposed rule
(74 FR 40948, 40957), we stated that
outlier payments increased as a
percentage of total payments from 4.1
percent in CY 2005, to 5.0 percent in CY
2006, to 6.4 percent in CY 2007 and that
this excessive growth in outlier
payments was primarily the result of
unusually high outlier payments in a
few areas of the country. In that
discussion, we noted that despite
program integrity efforts associated with
excessive outlier payments in targeted
areas of the country, we discovered that
outlier expenditures still exceeded the 5
percent target in CY 2007 and, in the
absence of corrective measures, would
continue do to so. Consequently, we
assessed the appropriateness of taking
action to curb outlier abuse. As
described in the CY 2010 HH PPS final
rule (74 FR 58080 through 58087), to
mitigate possible billing vulnerabilities
associated with excessive outlier
payments and adhere to our statutory
limit on outlier payments, we finalized
an outlier policy that included a 10
percent agency-level cap on outlier
payments. This cap was implemented in
concert with a reduced FDL ratio of
0.67. These policies resulted in a
projected target outlier pool of
approximately 2.5 percent. (The
previous outlier pool was 5 percent of
total home health expenditures). For CY
2010, we first returned the 5 percent
held for the previous target outlier pool
to the national, standardized 60-day
episode rates, the national per-visit
rates, the LUPA add-on payment
amount, and the NRS conversion factor.
Then, we reduced the CY 2010 rates by
2.5 percent to account for the new
outlier pool of 2.5 percent. This outlier
policy was adopted for CY 2010 only.
As we noted in the CY 2011 HH PPS
final rule (75 FR 70397 through 70399),
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section 3131(b)(1) of the Affordable Care
Act amended section 1895(b)(3)(C) of
the Act, and required the Secretary to
reduce the HH PPS payment rates such
that aggregate HH PPS payments were
reduced by 5 percent. In addition,
section 3131(b)(2) of the Affordable Care
Act amended section 1895(b)(5) of the
Act by redesignating the existing
language as section 1895(b)(5)(A) of the
Act, and revising the language to state
that the total amount of the additional
payments or payment adjustments for
outlier episodes may not exceed 2.5
percent of the estimated total HH PPS
payments for that year. Section
3131(b)(2)(C) of the Affordable Care Act
also added section 1895(b)(5)(B) of the
Act which capped outlier payments as
a percent of total payments for each
HHA at 10 percent.
As such, beginning in CY 2011, our
HH PPS outlier policy is that we reduce
payment rates by 5 percent and target
up to 2.5 percent of total estimated HH
PPS payments to be paid as outliers. To
do so, we returned the 2.5 percent held
for the target CY 2010 outlier pool to the
national, standardized 60-day episode
rates, the national per visit rates, the
LUPA add-on payment amount, and the
NRS conversion factor for CY 2010.
Then we reduced the rates by 5 percent
as required by section 1895(b)(3)(C) of
the Act, as amended by section
3131(b)(1) of the Affordable Care Act.
For CY 2011 and subsequent calendar
years we target up to 2.5 percent of
estimated total payments to be paid as
outlier payments, and apply a 10
percent agency-level outlier cap.
In the CY 2017 HH PPS proposed and
final rules (81 FR 43737 through 43742
and 81 FR 76724), we described our
concerns regarding patterns observed in
home health outlier episodes.
Specifically, we noted that the
methodology for calculating home
health outlier payments may have
created a financial incentive for
providers to increase the number of
visits during an episode of care to
surpass the outlier threshold and
simultaneously created a disincentive
for providers to treat medically complex
beneficiaries who require fewer but
longer visits. Given these concerns, in
the CY 2017 HH PPS final rule (81 FR
76724), we finalized changes to the
methodology used to calculate outlier
payments, using a cost-per-unit
approach rather than a cost-per-visit
approach. This change in methodology
allows for more accurate payment for
outlier episodes, accounting for both the
number of visits during an episode of
care and also the length of the visits
provided. Using this approach, we now
convert the national per-visit rates into
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per 15-minute unit rates. These per 15minute unit rates are used to calculate
the estimated cost of an episode to
determine whether the claim will
receive an outlier payment and the
amount of payment for an episode of
care. In conjunction with our finalized
policy to change to a cost-per-unit
approach to estimate episode costs and
determine whether an outlier episode
should receive outlier payments, in the
CY 2017 HH PPS final rule (81 FR
76725) we also finalized the
implementation of a cap on the amount
of time per day that would be counted
toward the estimation of an episode’s
costs for outlier calculation purposes.
Specifically, we limit the amount of
time per day (summed across the six
disciplines of care) to 8 hours (32 units)
per day when estimating the cost of an
episode for outlier calculation purposes.
2. Fixed Dollar Loss (FDL) Ratio
For a given level of outlier payments,
there is a trade-off between the values
selected for the FDL ratio and the losssharing ratio. A high FDL ratio reduces
the number of episodes that can receive
outlier payments, but makes it possible
to select a higher loss-sharing ratio, and
therefore, increase outlier payments for
qualifying outlier episodes.
Alternatively, a lower FDL ratio means
that more episodes can qualify for
outlier payments, but outlier payments
per episode must then be lower.
The FDL ratio and the loss-sharing
ratio must be selected so that the
estimated total outlier payments do not
exceed the 2.5 percent aggregate level
(as required by section 1895(b)(5)(A) of
the Act). Historically, we have used a
value of 0.80 for the loss-sharing ratio
which, we believe, preserves incentives
for agencies to attempt to provide care
efficiently for outlier cases. With a losssharing ratio of 0.80, Medicare pays 80
percent of the additional estimated costs
above the outlier threshold amount.
Simulations based on CY 2015 claims
data (as of June 30, 2016) completed for
the CY 2017 HH PPS final rule showed
that outlier payments were estimated to
represent approximately 2.84 percent of
total HH PPS payments in CY 2017, and
as such, we finalized a change to the
FDL ratio from 0.45 to 0.55. We stated
that raising the FDL ratio to 0.55, while
maintaining a loss-sharing ratio of 0.80,
struck an effective balance of
compensating for high-cost episodes
while still meeting the statutory
requirement to target up to, but no more
than, 2.5 percent of total payments as
outlier payments (81 FR 76726). The
national, standardized 60-day episode
payment amount is multiplied by the
FDL ratio. That amount is wage-adjusted
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to derive the wage-adjusted FDL
amount, which is added to the case-mix
and wage-adjusted 60-day episode
payment amount to determine the
outlier threshold amount that costs have
to exceed before Medicare would pay 80
percent of the additional estimated
costs.
Using preliminary CY 2016 claims
data (as of March 17, 2017) and the
proposed CY 2018 payment rates
presented in section III.C. of the CY
2018 HH PPS proposed rule (82 FR
35293), we estimated that outlier
payments would constitute
approximately 2.47 percent of total HH
PPS payments in CY 2018 under the
current outlier methodology. Given the
statutory requirement to target up to, but
no more than, 2.5 percent of total
payments as outlier payments, we did
not propose a change to the FDL ratio
for CY 2018 as we believed that
maintaining an FDL ratio of 0.55 with a
loss-sharing ratio of 0.80 was still
appropriate given the percentage of
outlier payments projected for CY 2018.
Likewise, we did not propose a change
to the loss-sharing ratio (0.80) for the
HH PPS to remain consistent with
payment for high-cost outliers in other
Medicare payment systems (for
example, Inpatient Rehabilitation
Facility (IRF) PPS, IPPS, etc.). While we
did not propose to change the FDL ratio
of 0.55 for CY 2018, we noted that we
would update our estimate of outlier
payments as a percent of total HH PPS
payments using the most current and
complete year of HH PPS data (CY 2016
claims data as of June 30, 2017 or later)
in this final rule.
Using updated CY 2016 claims data
(as of August 18, 2017) and the final CY
2018 payment rates presented in section
III.C of this final rule, we estimate that
outlier payments would continue to
constitute approximately 2.47 percent of
total HH PPS payments in CY 2018
under the current outlier methodology.
Given the statutory requirement to target
up to, but no more than, 2.5 percent of
total payments as outlier payments, we
continue to believe that maintaining an
FDL ratio of 0.55 with a loss-sharing
ratio of 0.80 is still appropriate given
the percentage of outlier payments
projected for CY 2018.
The following is a summary of the
comments received and our responses.
Comment: A commenter questioned if
we would provide the CY 2018 cost-perunit values to be used for the outlier
calculation.
Response: The cost-per-unit amounts
for CY 2018 are in Table 14 of this final
rule. We note that in the CY 2017 HH
PPS final rule (81 FR 76724), we stated
that we did not plan to re-estimate the
average minutes per visit by discipline
every year. Additionally, we noted that
the per-unit rates used to estimate an
episode’s cost will be updated by the
home health update percentage each
year, meaning we would start with the
national per-visit amounts for the same
calendar year when calculating the costper-unit used to determine the cost of an
episode of care (81 FR 76727).
TABLE 14—CY 2018 COST-PER-UNIT PAYMENT RATES FOR THE CALCULATION OF OUTLIER PAYMENTS *
CY 2018
National
per-visit
payment rates
Visit type
Home health aide ........................................................................................................................
Medical social services ................................................................................................................
Occupational therapy ...................................................................................................................
Physical therapy ..........................................................................................................................
Skilled nursing .............................................................................................................................
Speech-language pathology ........................................................................................................
$64.94
229.86
157.83
156.76
143.40
170.38
Average
minutesper-visit
63.0
56.5
47.1
46.6
44.8
48.1
Cost-per-unit
(1 unit = 15
minutes)
$15.46
61.02
50.26
50.46
48.01
53.13
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* These values reflect the national per visit rates for each discipline for providers who have submitted quality data; for rates applicable to those
providers who did not submit quality data submitted, please see our forthcoming CY 2018 Rate Update Change Request, which will be available
here: https://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/2017-Transmittals.html.
We note that we will continue to
monitor the visit length by discipline as
more recent data become available, and
we may propose to update the rates as
needed in the future.
Comment: Several commenters stated
that the changes to the outlier
methodology made in the CY 2017 final
rule, particularly the increase in the
FDL ratio from 0.45 to 0.55, were
significant and may have led to a
reduction in the number of home health
episodes that would qualify for outlier
payment. The commenters
recommended that CMS release data on
the impact of this policy change on the
dually eligible beneficiary population
and in particular those patients with
clinically complex conditions.
Response: We appreciate the
commenters’ concerns regarding the
potential impact of the changes to the
outlier policy finalized in the CY 2017
HH PPS final rule (81 FR 76727). Data
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reflecting the changes to the outlier
policy made for CY 2017 are not yet
available for analysis and assessment.
However, as these updated data become
available, we will evaluate for changes,
analyze patterns in home health outlier
payments, and monitor for any impacts,
particularly for those beneficiaries with
clinically complex conditions, and may
include the results of such efforts in
future rulemaking.
Additionally, as discussed in the CY
2017 HH PPS final rule (81 FR 76728),
the goal of this policy change is to more
accurately pay for outlier episodes. We
noted in the CY 2017 HH PPS proposed
rule that analysis indicates that a larger
percentage of episodes of care for
patients with a fragile overall health
status will qualify for outlier payments
(81 FR 43713). The outlier system is
meant to help address extra costs
associated with extra, and potentially
unpredictable, medically necessary care.
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In section II.D. of the CY 2018 HH PPS
proposed rule (82 FR 35275), we
discussed Report to Congress: Home
Health Study on Access to Care for
Vulnerable Patient Populations and
Subsequent Research and Analyses. We
believe that this change in the outlier
payment policy may ultimately serve to
address some of the findings from the
home health study, where margins were
lower for patients with medically
complex needs that typically require
longer visits, thus potentially creating
an incentive to treat only or primarily
patients with less complex needs.
Moreover, the 2.5 percent target of
outlier payments to total home health
payments is a statutory requirement, as
established in section 1895(b)(5) of the
Act. Therefore, we modified the FDL in
order to align the estimated outlier
payments with the 2.5 percent target
required by law.
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Comment: A few commenters
expressed disagreement with CMS’s
decision to maintain the existing 10percent cap on outlier payments to
HHAs as a purported fraud-fighting
effort, suggesting that a potentially more
appropriate and targeted fraud-fighting
initiative will include a possible
minimum provider-specific number or
percent of episodes that result in
LUPAs, suggesting that reporting
periods with zero LUPAs could be an
indicator of inappropriate provider
behavior.
Response: Regarding the
appropriateness of the 10 percent peragency cap, we note that the 2.5 percent
target of outlier payments to total home
health payments and the 10 percent cap
on outlier payments at the home health
agency level are statutory requirements,
as established in section 1895(b)(5) of
the Act. Therefore, we do not have the
authority to adjust or eliminate the 10percent cap or increase the 2.5 percent
target amount. Additionally, we
appreciate the commenter’s suggestion
regarding alternative approaches for
targeting fraud within the Medicare
home health benefit. The Program for
Evaluating Payment Patterns Electronic
Report (PEPPER) is a comparative data
report that summarizes a single
provider’s Medicare claims data
statistics for services vulnerable to
improper payments. PEPPER can
support a hospital or facility’s
compliance efforts by identifying where
its billing patterns are different from the
majority of other providers in the
nation. This data can help identify both
potential overpayments and potential
underpayments, and can provide
guidance on areas in which a provider
may want to focus auditing and
monitoring efforts with the goal of
preventing improper Medicare
payments. In the HHA PEPPER, we
include a metric for non-LUPA
payment, which represents the count of
episodes paid to the HHA that did not
have a LUPA payment during the report
period as a proportion of total episodes
paid to the HHA during the report
period (available at: https://
www.pepperresources.org/Portals/0/
Documents/PEPPER/HHA/HHA_
PEPPERUsersGuide_Edition2.pdf). This
measure is provided to the HHA
community for review and may also be
used by our Center for Program Integrity
as a guide for audits and other
investigative efforts.
We also note that, as described in the
CY 2017 HH PPS final rule (82 FR
76727), in 2015, only about 1 percent of
HHAs received 10 percent of their total
HH PPS payments as outlier payments,
while almost 71 percent of HHAs
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received less than 1 percent of their
total HH PPS payments as outliers.
Therefore, the 10 percent agency-level
cap does not seem to significantly
impact a large portion of HHAs.
Comment: Several commenters
recommended that CMS conduct a more
detailed analysis to determine whether
the total cap of 2.5 percent of total
payments as outlier payments is
adequate or whether it needs to be
increased for future years, particularly
given the expected change in Medicare
beneficiary demographics anticipated in
the coming years.
Response: As established in section
1895(b)(5) of the Act, both the 2.5
percent target of outlier payments to
total home health payments and the 10percent cap on outlier payments at the
home health agency level are statutory
requirements. Therefore, we do not have
the authority to adjust or eliminate the
10-percent cap or increase the 2.5percent target amount. However, we
will continue to evaluate for the
appropriateness of those elements of the
outlier policy that may be modified,
including the FDL and the loss-sharing
ratio. We note that other Medicare
payment systems with outlier payments,
such as the IRF PPS and IPPS, annually
reassess the fixed-loss cost outlier
threshold amount. Adjusting the outlier
threshold amount in order to target the
statutorily required percentage of total
payments as outlier payments is
standard practice.
Comment: A commenter
recommended that CMS eliminate
outlier payments in their entirety.
Response: We believe that section
1895(b)(5)(A) of the Act allows the
Secretary the discretion as to whether or
not to have an outlier policy under the
HH PPS. However, we also believe that
outlier payments are beneficial in that
they help mitigate the incentive for
HHAs to avoid patients that may have
episodes of care that result in unusual
variations in the type or amount of
medically necessary care. The outlier
system is meant to help address extra
costs associated with extra, and
potentially unpredictable, medically
necessary care. We note that we plan to
continue evaluating whether or not an
outlier policy remains appropriate as
well as ways to maintain an outlier
policy for episodes that incur unusually
high costs due to patient care needs.
Final Decision: We are finalizing no
change to the FDL ratio or loss sharing
ratio for CY 2018. We are maintaining
an FDL ratio of 0.55 with a loss-sharing
ratio of 0.80 for CY 2018. However, we
will continue to monitor outlier
payments and continue to explore ways
to maintain an outlier policy for
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episodes that incur unusually high
costs.
E. Proposed Implementation of the
Home Health Groupings Model (HHGM)
for CY 2019
We proposed case-mix methodology
refinements through the implementation
of the Home Health Groupings Model
(HHGM). We proposed to implement the
HHGM for home health periods of care
beginning on or after January 1, 2019.
The HHGM uses 30-day periods rather
than the 60-day episode used in the
current payment system, eliminates the
use of the number of therapy visits
provided to determine payment, and
relies more heavily on clinical
characteristics and other patient
information (for example, diagnosis,
functional level, comorbid conditions,
admission source) to place patients into
clinically meaningful payment
categories.
We are not finalizing the
implementation of the HHGM in this
final rule. We received many comments
from the public that we would like to
take into further consideration. While
commenters were generally supportive
of the concept of revising the HH PPS
case-mix methodology to better align
payments with the costs of providing
care, commenters included technical
comments on various aspects of the
proposed case-mix adjustment
methodology under the HHGM and
were most concerned about the
proposed change in the unit of payment
from 60 days to 30 days and such
change being proposed for
implementation in a non-budget neutral
manner. Commenters also stated their
desire for greater involvement in the
development of the HHGM and the need
for access to the necessary data in order
to replicate and model the effects on
their businesses.
We note that information continues to
be available to stakeholders around this
important initiative. The analyses and
the ultimate development of HHGM was
previously shared with both internal
and external stakeholders via technical
expert panels, clinical workgroups, and
special open door forums. We provided
high-level summaries on our case-mix
methodology refinement work in the HH
PPS proposed rules for CYs 2016 and
2017 (80 FR 39839, and 81 FR 76702).
Additionally, a detailed technical report
was posted on the CMS Web site in
December 2016 and remains available,
additional technical expert panel and
clinical workgroup webinars were held
after the posting of the technical report,
and a National Provider call occurred in
January 2017 to further solicit feedback
from stakeholders and the general
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public.12 As many did, any provider or
organization wishing to receive the
necessary data to replicate and model
the effects of the HHGM or study the
Medicare home health benefit can
submit a request through the CMS Data
Request Center.13 We note that the
Home Health Agency Limited Data Set
files and Research Identifiable Files are
available on a quarterly and annual
basis. The fourth quarter data for CY
2016 were available in mid-May of
2017. The fourth quarter files include all
final action fee-for-service claims
received by December 31, 2016. We also
posted a HHGM Groupings Tool along
with the CY 2018 HH PPS proposed rule
on the HHA Center Web page, which
providers can continue to use in order
to replicate the HHGM methodology
using their own internal data.
We also note that, in the CY 2018 HH
PPS proposed rule, we assumed that
behavioral responses would occur upon
implementation of the HHGM. If no
behavioral assumptions were made and
we implemented the HHGM for CY
2018, we estimate that the 30-day
payment amount needed to achieve
budget neutrality would have been
$1,722.29. However, because we have a
continued fiduciary duty as stewards of
the Medicare program to mitigate
potential overpayments, if possible, we
assumed behavioral responses would
occur in the estimation of the 30-day
payment amount. We determined that, if
the HHGM were implemented for CY
2018 with assumed behavioral
responses, the 30-day payment amount
needed to achieve budget neutrality
would have been $1,622.61. For the CY
2018 HH PPS proposed rule, we
included two behavioral assumptions in
our impact estimates related to the
proposed implementation of the HHGM
for CY 2019: (1) For LUPAs one visit
under the proposed HHGM case-mix
group thresholds, HHAs would provide
an additional visit so the 30-day period
of care becomes a non-LUPA; and (2)
the highest-paying diagnosis code
would be listed as primary for clinical
grouping assignment. While we do not
support or condone coding practices or
the provision of services solely to
maximize payment, we often take into
account expected behavioral effects of
policy changes related to rate setting.
We included a LUPA behavioral
assumption in our estimated impact of
the HHGM based on past behavioral
assumptions made under the HH PPS.
12 https://www.cms.gov/Outreach-and-Education/
Outreach/NPC/National-Provider-Calls-and-EventsItems/2017-01-18-Home-Health.html.
13 https://www.resdac.org/cms-data/request/cmsdata-request-center.
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As noted in the FY 2001 HH PPS final
rule, the episode file showed that
approximately 16 percent of episodes
would have received a LUPA (65 FR
41162). However, currently, about 7
percent of all 60-day episodes receive a
LUPA. For the HHGM, approximately 7
percent of 30-day periods would receive
a LUPA. However, because 4.9 percent
of 30-day periods of care are just one
visit below the LUPA thresholds under
the HHGM, we assume that for these 30day periods, HHAs will provide an
additional visit to avoid receiving a
LUPA, especially in the absence of
therapy thresholds and the change from
a 60-day to 30-day unit of payment.
With regards to our assumption that
HHAs would code the highest-paying
diagnosis code as primary for the
clinical grouping assignment, this
assumption was based on decades of
past experience under the HH PPS and
other case-mix systems, such as the
implementation of the diagnosis-related
groups (DRGs) and the Medicare
Severity (MS)-DRGs under the inpatient
prospective payment system. In the FY
2008 IPPS final rule (72 FR 47176), we
noted that case-mix refinements can
lead to substantial unwarranted increase
in payments. To address this issue when
CMS transitioned from DRGs to MS–
DRGs, MedPAC recommended that the
Secretary project the likely effect of
reporting improvements on total
payments and make an offsetting
adjustment to the national average base
payment amounts (72 FR 47176). In the
FY 2008 IPPS final rule (72 FR 47181),
we summarized instances where casemix increases resulted from
documentation and coding-induced
changes for the first year of the IRF PPS
and in Maryland hospitals’ transition to
APR DRGs (estimated at around 5
percent in both instances). Therefore,
we estimated that an adjustment of 4.8
percent would be necessary to maintain
budget neutrality for the transition to
the MS–DRGs (72 FR 47178). With
regards to experience under the HH
PPS, as outlined in the CY 2018 HH PPS
proposed rule (82 FR 35274), between
CY 2000 and 2010, total case-mix
change was 23.90 percent, with 20.08
considered nominal case-mix growth, an
average of approximately 2 percent
nominal case-mix growth per year.
IV. Provisions of the Home Health
Value-Based Purchasing (HHVBP)
Model
A. Background
As authorized by section 1115A of the
Act and finalized in the CY 2016 HH
PPS final rule (80 FR 68624), we began
testing the HHVBP Model on January 1,
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2016. The HHVBP Model has an overall
purpose of improving the quality and
delivery of home health care services to
Medicare beneficiaries. The specific
goals of the Model are to: (1) Provide
incentives for better quality care with
greater efficiency; (2) study new
potential quality and efficiency
measures for appropriateness in the
home health setting; and (3) enhance the
current public reporting process.
Using the randomized selection
methodology finalized in the CY 2016
HH PPS final rule, nine states were
selected for inclusion in the HHVBP
Model, representing each geographic
area across the nation. All Medicarecertified HHAs providing services in
Arizona, Florida, Iowa, Maryland,
Massachusetts, Nebraska, North
Carolina, Tennessee, and Washington
(competing HHAs) are required to
compete in the Model. Requiring all
Medicare-certified HHAs providing
services in the selected states to
participate in the Model ensures that:
(1) There is no selection bias; (2)
participating HHAs are representative of
HHAs nationally; and, (3) there is
sufficient participation to generate
meaningful results.
As finalized in the CY 2016 HH PPS
final rule, the HHVBP Model will utilize
the waiver authority under section
1115A(d)(1) of the Act to adjust
Medicare payment rates under section
1895(b) of the Act beginning in CY 2018
based on performance on applicable
measures. Payment adjustments will be
increased incrementally over the course
of the HHVBP Model in the following
manner: (1) A maximum payment
adjustment of 3 percent (upward or
downward) in CY 2018; (2) a maximum
payment adjustment of 5 percent
(upward or downward) in CY 2019; (3)
a maximum payment adjustment of 6
percent (upward or downward) in CY
2020; (4) a maximum payment
adjustment of 7 percent (upward or
downward) in CY 2021; and (5) a
maximum payment adjustment of 8
percent (upward or downward) in CY
2022. Payment adjustments will be
based on each HHA’s Total Performance
Score (TPS) in a given performance year
(PY) on: (1) A set of measures already
reported via OASIS and HHCAHPS for
all patients serviced by the HHA and
select claims data elements; and (2)
three new measures where points are
achieved for reporting data.
In the CY 2017 HH PPS final rule (81
FR 76741 through 76752), in addition to
providing an update on the progress
towards developing public reporting of
performance under the HHVBP Model,
we finalized the following changes
related to the HHVBP Model:
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• Calculating benchmarks and
achievement thresholds at the state level
rather than the level of the size-cohort
and revising the definition for
benchmark to state that benchmark
refers to the mean of the top decile of
Medicare-certified HHA performance on
the specified quality measure during the
baseline period, calculated for each
state.
• Requiring a minimum of eight
HHAs in a size-cohort.
• Increasing the timeframe for
submitting new measure data from
seven calendar days to 15 calendar days
following the end of each reporting
period to account for weekends and
holidays.
• Removing four measures (Care
Management: Types and Sources of
Assistance, Prior Functioning Activities
of Daily Living (ADL)/Instrumental ADL
(IADL), Influenza Vaccine Data
Collection Period, and Reason
Pneumococcal Vaccine Not Received)
from the set of applicable measures.
• Adjusting the reporting period and
submission date for the Influenza
Vaccination Coverage for Home Health
Personnel measure from a quarterly
submission to an annual submission.
• Allowing for an appeals process
that includes the recalculation process
finalized in the CY 2016 HH PPS final
rule (80 FR 68688 through 68689), as
modified, and adds a reconsideration
process.
B. Quality Measures
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1. Adjustment to the Minimum Number
of Completed Home Health Care
Consumer Assessment of Healthcare
Providers and System (HHCAHPS)
Surveys
The HHCAHPS survey presents home
health patients with a set of
standardized questions about their
home health care providers and about
the quality of their home health care.
The survey is designed to measure the
experiences of people receiving home
health care from Medicare-certified
home health care agencies and meet the
following three broad goals to: (1)
Produce comparable data on the
patient’s perspective that allows
objective and meaningful comparisons
between HHAs on domains that are
important to consumers; (2) create
incentives through public reporting of
survey results for agencies to improve
their quality of care; and (3) enhance
public accountability in health care by
increasing the transparency of the
quality of care provided in return for
public investment through public
reporting.
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As finalized in the CY 2016 HH PPS
final rule (80 FR 68685 through 68686),
if a HHA does not have a minimum of
20 episodes of care during a
performance year (PY) to generate a
performance score on at least five
measures, that HHA would not be
included in the Linear Exchange
Function (LEF) and would not have a
payment adjustment percentage
calculated. The LEF is used to translate
an HHA’s Total Performance Score
(TPS) into a percentage of the valuebased payment adjustment earned by
each HHA under the HHVBP Model. For
the HHCAHPS measures, a minimum of
20 HHCAHPS completed surveys would
be necessary in order for scores to be
generated for the HHCAHPS quality
measures that can be included in the
calculation of the TPS.
However, as we stated in the CY 2018
HH PPS proposed rule (82 FR 35333),
we believe that using a minimum of 40
completed HHCAHPS surveys, rather
than a minimum of 20 completed
HHCAHPS surveys, will better align the
Model with HHCAHPS policy for the
Patient Survey Star Ratings on Home
Health Compare.14 The decision to use
a minimum of 40 completed surveys for
these star ratings was a result of
balancing two competing goals. One
goal was to provide star ratings that
were meaningful and minimized
random variations. This goal was best
served by calculating star ratings for
large numbers of cases by having a
larger minimum of completed
HHCAHPS surveys (for example, 50 or
100 completed HHCAHPS surveys). At
the same time, we also wanted to be
able to provide star ratings for as many
HHAs as possible. This goal was best
served by using a lower minimum of
completed HHCAHPS surveys (for
example, 20 completed HHCAHPS
surveys). We chose to balance these
opposing and necessary goals by using
40 completed HHCAHPS surveys for the
Patient Survey Star Ratings. Because we
believe that aligning the Patient Survey
Star Ratings system and the HHVBP
Model provides uniformity, consistency,
and standard transformability for
different healthcare platforms, we
proposed using a minimum of 40
instead of 20 completed HHCAHPS
surveys under the HHVBP Model (82 FR
35333).
In the CY 2018 HH PPS proposed rule
(82 FR 35333), we noted that we
received a comment in response to the
CY 2016 HH PPS proposed rule in
support of using a higher minimum
14 Patient Survey Star Ratings https://
www.medicare.gov/HomeHealthCompare/Data/
Patient-Survey-Star-Ratings.html.
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threshold for HHCAHPS completed
surveys for the Patient Survey Star
Ratings if the data are going to be used
in HHVBP or any other quality
assessment program. We also noted that
we received public comment in
response to the CY 2017 HH PPS
proposed rule in support of using a
higher minimum threshold for
HHCAHPS completed surveys in the
HHVBP Model, including a
recommendation to use a minimum of
100 HHCAHPS rather than a sample size
of 20 surveys (82 FR 35333). We stated
in the CY 2018 HH PPS proposed rule
(82 FR 35333) that we believe that
proposing a minimum of 40 completed
HHCAHPS surveys for the Model would
be more appropriate than the higher
minimums previously recommended by
some commenters because it represents
a balance between providing meaningful
data and having sufficient numbers of
HHAs with performance scores for at
least 5 measures in the cohorts.
Moreover, using a minimum of 40
completed HHCAHPS surveys aligns
with the Patient Survey Star Ratings on
Home Health Compare (82 FR 35333).
To understand the possible impact of
our proposal to use a minimum of 40
HHCAHPS completed surveys, we noted
in the CY 2018 HH PPS proposed rule
(82 FR 35333) that HHAs may refer to
the Interim Performance Reports (IPRs)
issued in October 2016, January 2017
and April 2017, which analyzed 40 or
more completed HHCAHPS surveys to
determine each HHA’s HHCAHPS
quality measure scores. As a point of
comparison to the minimum of 40
HHCAHPS completed surveys, these
IPRs were reissued using a minimum of
20 or more completed HHCAHPS
surveys and included quality measure
scores, for these same time periods,
calculated with HHAs that qualify for
the LEF by having sufficient data for at
least five measures. HHAs had the
opportunity to submit a request for
recalculation of the revised interim
performance scores.
HHAs had an opportunity to evaluate
these IPRs in light of the proposal to
change to a minimum of 40 HHCAHPS
completed surveys, as well as seek
clarification on the difference in their
reports. The participating HHAs
received concurrent IPRs in July 2017
and concurrent Annual Total
Performance Score and Payment
Adjustment Reports, which we made
available in August 2017. The
concurrent reports showed one report
with HHCAHPS quality measure scores
calculated based on a minimum of 40
completed surveys and one report with
HHCAHPS quality measure scores
calculated based on a minimum of 20
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completed surveys. Because the CY
2018 HH PPS proposed rule would not
be finalized before the timeline for
submission of recalculation and
reconsideration requests, we noted
HHAs would have the opportunity to
submit recalculation requests for the
interim performance scores based on
both a minimum of 40 and 20
completed surveys, and recalculation
and reconsideration requests, as
applicable, for the annual total
performance scores included in these
reports for these thresholds in
accordance with the appeals process set
forth at § 484.335, which was finalized
in the CY 2017 HH PPS final rule (82
FR 35333).
As discussed in the CY 2018 HH PPS
proposed rule (82 FR 35333 through
35334), we analyzed the effects on
participating HHAs of using the
proposed 40 or more completed
HHCAHPS surveys as compared to
using 20 or more completed HHCAHPS
surveys by examining OASIS measures
submitted from January 1, 2015 through
December 31, 2016, claims measures
submitted from September 1, 2015
through September 30, 2016, and 12
months ending June 30, 2016 for
HHCAHPS-based measures. We found
that achievement thresholds, which are
calculated as the median of all HHAs’
performance on the specified quality
measures during the 2015 baseline year
for each state, would not change by
more than ±1.1 percent, with the largest
changes occurring in the statewide
achievement thresholds for the
HHCAHPS Willingness to Recommend
the Agency measure in Arizona (+1.1
percent) and Nebraska (¥1.1 percent).
Benchmarks (the mean of the top decile
of Medicare-certified HHA performance
on the specified quality measures
during the 2015 baseline year,
calculated for each state) had greater
potential for change, ranging down to
¥3.2 percent. For instance, we found
that when calculated using a minimum
of 40 surveys rather than a minimum of
20 surveys, there was a ¥2.0 percent
change in the benchmark for the
HHCAHPS Willingness to Recommend
the Agency measure for Arizona and a
¥1.7 percent change in the benchmark
for Nebraska. We also found that when
calculated using a minimum of 40
surveys rather than a minimum of 20
surveys, there was a ¥1.7 percent
change in the benchmark for the
HHCAHPS Communications between
Providers and Patients measure for
Arizona, a ¥1.7 percent change in the
benchmark for Florida, and a ¥3.2
percent change in the benchmark for
Nebraska. Overall, the proposed change
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in the HHCAHPS minimum of 40
completed surveys was estimated to
result in a limited percent change in the
average statewide TPS for larger-volume
HHAs, ranging from ¥0.4 through +2.2
percent. We provided estimates of the
expected payment adjustment
distribution based on the proposed
minimum of 40 completed HHCAHPS
surveys in the impact analysis of the CY
2018 HH PPS proposed rule (82 FR
35387).’’
We invited public comment on our
proposal to use 40 or more completed
HHCAHPS surveys as the minimum to
generate a quality measure score on the
HHCAHPS measures, as is currently
used in Home Health Compare and the
Patient Survey Star Ratings. Therefore,
we proposed to revise the definition of
‘‘applicable measure’’ at § 484.305 from
a measure for which the competing
HHA has provided 20 home health
episodes of care per year to a measure
for which a competing HHA has
provided a minimum of 20 home health
episodes of care per year for the OASISbased measures, 20 home health
episodes of care per year for the claimsbased measures, or 40 completed
surveys for the HHCAHPS measures. We
proposed that if finalized, this policy
would apply to the calculation of the
benchmark and achievement thresholds
and the calculation of performance
scores for all Model years, beginning
with PY 1.
The following is a summary of the
public comments received on this
proposal and our responses:
Comment: Most commenters
supported CMS’ proposal to adjust the
minimum number of completed Home
Health Care Consumer Assessment of
Healthcare Providers and System
(HHCAHPS) Surveys. Several of these
commenters expressed that it will result
in more reliable and valid data results,
as well as better align with the Patient
Survey Star Ratings policy. A few
commenters expressed concern about
the proposed change and that using a
minimum of 40 completed HHCAHPS
surveys will greatly reduce the number
of agencies with data sufficient for
Model participation. A commenter
specifically requested that CMS provide
a clear and separate announcement
regarding the change in survey
minimum, how to interpret changes in
total performance scores, and how to
engage in the appeals process. Finally,
a few commenters were concerned that
smaller volume agencies will be
negatively impacted, or forced to close,
given the shift from 20 to 40 completed
HHCAHPS surveys.
Response: We appreciate commenters’
support for our proposal to use a
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minimum of 40 completed HHCAHPS
surveys, rather than a minimum of 20
completed HHCAHPS surveys. We
continue to believe that a minimum of
40 completed HHCAHPS surveys, rather
than a minimum of 20 completed
HHCAHPS surveys, better aligns the
Model with HHCAHPS policy for the
Patient Survey Star Ratings on Home
Health Compare. As discussed in the
proposed rule, we believe that aligning
the Patient Survey Star Ratings and the
HHVBP Model will provide uniformity,
consistency, and standard
transformability for different healthcare
platforms. While we recognize that this
change could result in fewer agencies
receiving a measure score on the
HHCAHPS measures, we believe, as
indicated in the proposed rule, that
using a minimum of 40 completed
HHCAHPS surveys represents an
appropriate balance between providing
meaningful data and having sufficient
numbers of HHAs with performance
scores on five other measures (for
example OASIS based and claims based)
to be included in the LEF. As we
discuss later in this section, however,
our updated analysis using full CY 2016
data found that no HHA fell below the
minimum of having five measures to
generate a TPS as a result of using a
minimum of 40 rather than 20
completed HHCAHPs surveys.
For purposes of this final rule, we
analyzed the effects on participating
HHAs of using the proposed 40 or more
completed HHCAHPS surveys as
compared to using 20 or more
completed HHCAHPS surveys by
examining OASIS, claims and
HHCAHPS measures from January 1,
2016 to December 31, 2016. We found
that achievement thresholds will not
change by more than ±1.1 percent, with
the largest changes occurring in the
statewide achievement thresholds for
the HHCAHPS Willingness to
Recommend the Agency measure in
Arizona (+1.1 percent) and Nebraska
(¥1.1 percent). Benchmarks continued
to have greater potential for change,
ranging down to ¥3.1 percent. For
instance, we found that when calculated
using a minimum of 40 surveys rather
than a minimum of 20 surveys, there
was a ¥2.0 percent change in the
benchmark for the HHCAHPS
Willingness to Recommend the Agency
measure for Arizona and a ¥1.7 percent
change in the benchmark for Nebraska.
We also found that when calculated
using a minimum of 40 surveys rather
than a minimum of 20 surveys, there
was a ¥1.6 percent change in the
benchmark for the HHCAHPS
Communications between Providers and
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Patients measure for Arizona, a ¥1.7
percent change in the benchmark for
Florida, and a ¥3.1 percent change in
the benchmark for Nebraska.
Overall, based on this updated
analysis using full CY 2016 data, the
proposed change in the HHCAHPS
minimum of 40 completed surveys was
estimated to result in a limited percent
change in the average statewide TPS for
larger-volume HHAs, ranging from ¥0.3
percent through +1.8 percent and the
majority of the states were close to zero.
Additionally, the updated analysis
using full CY 2016 data found that there
were no Medicare-certified HHAs in the
selected states that fell below the
minimum of having five measures to
generate a TPS for CY 2018 as a result
of using a minimum of 40 rather than
20 completed HHCAHPs surveys.
To provide HHAs with information on
the effects of using a minimum of 40
completed HHCAHPS surveys, rather
than a minimum of 20 completed
HHCAHPS surveys, we reissued the
October 2016, January 2017 and April
2017 IPRs, which analyzed 40 or more
completed HHCAHPS surveys, so that
they could be recalculated with HHAs
that have 20 or more completed
HHCAHPS surveys. Moreover, CMS
provided HHAs with concurrent IPRs in
July 2017 and concurrent Annual Total
Performance Score and Payment
Adjustment Reports in August 2017 to
show one report with HHCAHPS quality
measure scores calculated based on a
minimum of 40 completed surveys and
one report with HHCAHPS quality
measure scores calculated based on a
minimum of 20 completed surveys.
HHAs also had the opportunity to
submit recalculation requests for the
interim performance scores and
recalculation and reconsideration
requests, as applicable, for the annual
total performance scores, in accordance
with the process set forth at § 484.335.
Additionally, we provided a number of
webinars and other information on the
interpretation of the quality measure
scores and the Total Performance Scores
and on the appeals process. More
specifically, we provided all HHAs with
a questions and answers document on
the use of HHCAHPS measures in
HHVBP Model performance reports
when the reissued and concurrent IPRs
were made available. These reports and
communications provided points of
comparison, clarification and
information on the potential impact of
using a minimum of 40 completed
HHCAHPS surveys, rather than a
minimum of 20 completed HHCAHPS
surveys, to generate a quality measure
score on the HHCAHPS measures. CMS
notes that no recalculation requests on
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the reissued and concurrent IPRs were
received and no recalculation or
reconsideration requests on the
concurrent Annual Reports were
received that related to our proposal to
change to the minimum of 40 completed
HHCAHPS surveys.
The change from a minimum of 20
completed HHCAHPS surveys to a
minimum of 40 completed HHCAHPS
surveys was not intended to negatively
impact smaller agencies. We do not
believe smaller HHAs will be
disadvantaged by this change to a
minimum of 40, because given their
exemption from HHCAHPS reporting
requirements, it is unlikely they would
be measured on HHCAHPS under the
Model and they can still compete on
other measures.
We will continue to monitor the
impacts of using a minimum of 40
completed HHCAHPS surveys, rather
than a minimum of 20 completed
HHCAHPS surveys, for purposes of
receiving a performance score for any of
the HHCAHPS measures.
Comment: A commenter suggested
that because one negative survey might
affect a score based on a minimum of 20
completed HHCAHPS surveys,
removing the lowest and highest
HHCAHPS for HHAs may be an
effective method to align with the
average customer response.
Response: We believe this comment is
outside of the scope of the proposed
methodology change in the CY 2018 HH
PPS proposed rule to use a minimum of
40 completed HHCAHPS surveys rather
than a minimum of 20 completed
HHCAHPS surveys. However, we note
that we believe each HHCAHPS survey
may be an important avenue for public
quality reporting and continued
improvement within the HHA
environment.
Final Decision: For the reasons stated
previously and in consideration of the
comments received, we are finalizing
our proposal to amend the definition of
‘‘applicable measure’’ to mean a
measure for which a competing HHA
has provided a minimum of 40
completed surveys for HHCAHPS
measures, for purposes of receiving a
performance score for any of the
HHCAHPS measures, beginning with
PY1. In addition, we are finalizing a few
minor technical edits to the regulation
at § 484.305 to replace the colon and
spell out ‘‘twenty’’ and ‘‘forty’’ (rather
than ‘‘20’’ and ‘‘40’’).
2. Removal of One OASIS-Based
Measure Beginning With Performance
Year 3
In the CY 2016 HH PPS final rule, we
finalized a set of quality measures in
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51703
Figure 4a: Final PY1 Measures and
Figure 4b: Final PY1 new measures (80
FR 68671 through 68673) for the
HHVBP Model to be used in PY 1,
referred to as the starter set.
The measures were selected for the
Model using the following guiding
principles: (1) Use a broad measure set
that captures the complexity of the
services HHAs provide; (2) Incorporate
the flexibility for future inclusion of the
Improving Medicare Post-Acute Care
Transformation Act of 2014 (IMPACT)
measures that cut across post-acute care
settings; (3) Develop ‘second generation’
(of the HHVBP Model) measures of
patient outcomes, health and functional
status, shared decision making, and
patient activation; (4) Include a balance
of process, outcome and patient
experience measures; (5) Advance the
ability to measure cost and value; (6)
Add measures for appropriateness or
overuse; and (7) Promote infrastructure
investments. This set of quality
measures encompasses the multiple
National Quality Strategy (NQS)
domains 15 (80 FR 68668). The NQS
domains include six priority areas
identified in the CY 2016 HH PPS final
rule (80 FR 68668) as the CMS
Framework for Quality Measurement
Mapping. These areas are: (1) Clinical
quality of care; (2) care coordination; (3)
population & community health; (4)
person- and caregiver-centered
experience and outcomes; (5) safety; and
(6) efficiency and cost reduction.
Figures 4a and 4b of the CY 2016 HH
PPS final rule (80 FR 68671 through
68673) identified 15 outcome measures
(five from the HHCAHPS, eight from
Outcome and Assessment Information
Set (OASIS), and two from the Chronic
Care Warehouse (claims)), and nine
process measures (six from OASIS, and
three new measures, which were not
previously reported in the home health
setting).
In the CY 2017 HH PPS final rule (81
FR 76743 through 76747), we removed
the following four measures from the
measure set for PY 1 and subsequent
performance years: (1) Care
Management: Types and Sources of
Assistance; (2) Prior Functioning ADL/
IADL; (3) Influenza Vaccine Data
Collection Period: Does this episode of
care include any dates on or between
October 1 and March 31?; and (4)
Reason Pneumococcal Vaccine Not
Received, for the reasons discussed in
that final rule.
For PY 3, we proposed to remove one
OASIS-based measure, Drug Education
15 2015 Annual Report to Congress, https://
www.ahrq.gov/workingforquality/reports/annualreports/nqs2015annlrpt.htm.
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on All Medications Provided to Patient/
Caregiver during All Episodes of Care,
from the set of applicable measures (82
FR 35334). We stated in the CY 2018 HH
PPS proposed rule that, as part of our
ongoing monitoring efforts, we found
that based on the standard metrics of
measure performance, many providers
have achieved full performance on the
Drug Education measure. For example,
for the January 2017 IPRs (which
covered the 12-month period of October
1, 2015 through September 30, 2016),
the average value for this measure
across all participating HHAs was 95.69
percent from October 2015 through
September 2016. When looking at
September 2016, the mean value on this
measure across all participating HHAs
had increased to 97.8 percent. In
addition, we noted that there are few
HHAs with poor performance on the
measure. Based on the January 2017
IPRs, across all participating HHAs, the
10th percentile was 89 percent and the
5th percentile was 81.8 percent, but
only 1.8 percent of HHAs had a value
below 70 percent on the measure. We
stated in the CY 2018 HH PPS proposed
rule (82 FR 35334) that we believe that
removing this measure would be
consistent with our policy, as noted in
the CY 2017 HH PPS final rule (81 FR
76746), that when a measure has
achieved full performance, we may
propose the removal of the measure in
future rulemaking. In addition, our
contractor’s Technical Expert Panel
(TEP), which consists of 11 panelists
with expertise in home health care and
quality measures, expressed concern
that the Drug Education measure does
not capture whether the education
provided by the HHA was meaningful.
We presented the revised set of
applicable measures, reflecting our
proposal to remove the OASIS-based
measure, Drug Education on All
Medications Provided to Patient/
Caregiver during All Episodes of Care,
in Table 43 of the CY 2018 HH PPS
proposed rule. We stated that this
measure set would be applicable to PY3
and each subsequent performance year
until such time that another set of
applicable measures, or changes to this
measure set, are proposed and finalized
in future rulemaking (82 FR 35334
through 35336).
We invited public comment on the
proposal to remove one OASIS-based
measure, Drug Education on All
Medications Provided to Patient/
Caregiver during All Episodes of Care,
from the set of applicable measures for
PY3 and subsequent performance years
and Table 43 of the CY 2018 HH PPS
proposed rule. The following is a
summary of the public comments
received on this proposal and our
responses:
Comment: Several commenters
expressed support for removing the
OASIS-based quality measure, Drug
Education on All Medications Provided
to Patient/Caregiver during All Episodes
of Care, from the set of applicable
measures as it has ‘‘topped out.’’
Response: We appreciate the support
regarding the proposed removal of the
‘‘Drug Education’’ measure from the
HHVBP Model’s set of applicable
measures because it has ‘‘topped out’’.
We are finalizing the removal of the
‘‘Drug Education’’ measure as most
providers have achieved full
performance on the measure.
Comment: Several commenters
provided feedback regarding the
measure set more generally and some
were outside of the scope of the
proposed change. A commenter
recommended that CMS consider
assigning 50 percent of the ‘‘Star
Rating’’ and HHVBP performance to
claims-based measures and Patient
Satisfaction, as the commenter believed
that these measures are difficult or
impossible to manipulate, and then
assign the other 50 percent to OASISbased self-reported measures. A
commenter expressed concern that the
measure set for the HHVBP Model
mainly requires improvement in patient
functioning and that this conflicts
directly with the Jimmo v. Sebelius
settlement.16 Another commenter
recommended replacing the
Pneumococcal Polysaccharide Vaccine
Ever Received (NQF#0525) because the
measure no longer reflects current
recommendations of the Advisory
Committee for Immunization Practice
(ACIP).
Response: We appreciate the
comments on the measures
methodology and, as discussed in the
CY 2016 HH PPS final rule (80 FR
68669) and CY 2017 HH PPS final rule
(81 FR 76747), acknowledge that skilled
care may be necessary to improve a
patient’s current condition, to maintain
the patient’s current condition, or to
prevent or slow further deterioration of
the patient’s condition, as was clarified
through the provisions revised as part of
Jimmo v. Sebelius settlement. As stated
in those rules, this settlement agreement
pertains only to the clarification of
CMS’s manual guidance on coverage
standards, not payment measures like
those at issue here, and expressly does
not pertain to or prevent the
implementation of new regulations,
including new regulations pertaining to
the HHVBP Model. We refer readers to
the CY 2016 HH PPS final rule (80 FR
68669 through 68670) for additional
discussion of our analyses of measure
selection, including our analyses of
existing measures relating to
improvement and stabilization. As
discussed in that rule, the HHVBP
Model is designed such that any
measures determined to be good
indicators of quality will be considered
for use in the HHVBP Model in future
years and may be added through the
rulemaking process. As discussed in
prior years, we will continue to seek
and consider input we have received on
the measure set for the HHVBP Model.
Final Decision: We are finalizing our
proposal to remove the OASIS-based
measure, Drug Education on All
Medications Provided to Patient/
Caregiver during All Episodes of Care,
from the set of applicable measures for
PY3 and subsequent years, as reflected
in Table 15. Table 15 identifies the
applicable measures set for PY3 and
each subsequent performance year until
such time that another set of applicable
measures, or changes to this measure
set, are proposed and finalized in future
rulemaking.
TABLE 15—MEASURE SET FOR THE HHVBP MODEL* BEGINNING PY 3
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NQS domains
Clinical Quality of
Care.
Measure title
Measure type
Identifier
Improvement in
Ambulation-Locomotion.
Outcome .......
NQF0167 ......
16 Jimmo v. Sebelius Settlement Agreement Fact
Sheet: https://www.cms.gov/Medicare/Medicare-
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Data source
OASIS
(M1860).
Numerator
Denominator
Number of home health episodes
of care where the value recorded
on the discharge assessment indicates less impairment in ambulation/locomotion at discharge
than at the start (or resumption)
of care.
Number of home health episodes
of care ending with a discharge
during the reporting period, other
than those covered by generic or
measure-specific exclusions.
Fee-for-Service-Payment/SNFPPS/Downloads/
Jimmo-FactSheet.pdf.
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TABLE 15—MEASURE SET FOR THE HHVBP MODEL* BEGINNING PY 3—Continued
Measure title
Measure type
Identifier
Clinical Quality of
Care.
Improvement in
Bed Transferring.
Outcome .......
NQF0175 ......
OASIS
(M1850).
Clinical Quality of
Care.
Improvement in
Bathing.
Outcome .......
NQF0174 ......
OASIS
(M1830).
Clinical Quality of
Care.
Improvement in
Dyspnea.
Outcome .......
NA .................
OASIS
(M1400).
Communication &
Care Coordination.
Discharged to
Community.
Outcome .......
NA .................
OASIS
(M2420).
Efficiency & Cost
Reduction.
Acute Care Hospitalization: Unplanned Hospitalization during first 60
days of Home
Health.
Outcome .......
NQF0171 ......
CCW (Claims)
Number of home health stays for
patients who have a Medicare
claim for an unplanned admission to an acute care hospital in
the 60 days following the start of
the home health stay.
Efficiency & Cost
Reduction.
Emergency Department Use
without Hospitalization.
Outcome .......
NQF0173 ......
CCW (Claims)
Number of home health stays for
patients who have a Medicare
claim for outpatient emergency
department use and no claims
for acute care hospitalization in
the 60 days following the start of
the home health stay.
Patient Safety .......
Improvement in
Pain Interfering
with Activity.
Outcome .......
NQF0177 ......
OASIS
(M1242).
Patient Safety .......
Improvement in
Management of
Oral Medications.
Outcome .......
NQF0176 ......
OASIS
(M2020).
Population/Community Health.
Influenza Immunization Received for Current Flu Season.
Process .........
NQF0522 ......
OASIS
(M1046).
Population/Community Health.
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NQS domains
Pneumococcal
Polysaccharide
Vaccine Ever
Received.
Process .........
NQF0525 ......
OASIS
(M1051).
Number of home health episodes
of care where the value recorded
on the discharge assessment indicates less frequent pain at discharge than at the start (or resumption) of care.
Number of home health episodes
of care where the value recorded
on the discharge assessment indicates less impairment in taking
oral medications correctly at discharge than at start (or resumption) of care.
Number of home health episodes
during which patients (a) received vaccination from the HHA
or (b) had received vaccination
from HHA during earlier episode
of care, or (c) was determined to
have received vaccination from
another provider.
Number of home health episodes
during which patients were determined to have ever received
Pneumococcal
Polysaccharide
Vaccine (PPV).
Patient & Caregiver-Centered
Experience.
Patient & Caregiver-Centered
Experience.
Care of Patients
Outcome .......
.......................
CAHPS .........
NA ...................................................
Number of home health episodes
of care ending with discharge or
transfer to inpatient facility during
the reporting period, other than
those covered by generic or
measure-specific exclusions.
NA.
Communications
between Providers and Patients.
Specific Care
Issues.
Outcome .......
.......................
CAHPS .........
NA ...................................................
NA.
Outcome .......
.......................
CAHPS .........
NA ...................................................
NA.
Overall rating of
home health
care.
Outcome .......
.......................
CAHPS .........
NA ...................................................
NA.
Patient & Caregiver-Centered
Experience.
Patient & Caregiver-Centered
Experience.
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Data source
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Numerator
Denominator
Number of home health episodes
of care where the value recorded
on the discharge assessment indicates less impairment in bed
transferring at discharge than at
the start (or resumption) of care.
Number of home health episodes
of care where the value recorded
on the discharge assessment indicates less impairment in bathing at discharge than at the start
(or resumption) of care.
Number of home health episodes
of care where the discharge assessment indicates less dyspnea
at discharge than at start (or resumption) of care.
Number of home health episodes
where the assessment completed
at the discharge indicates the patient remained in the community
after discharge.
Number of home health episodes
of care ending with a discharge
during the reporting period, other
than those covered by generic or
measure-specific exclusions.
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07NOR2
Number of home health episodes
of care ending with a discharge
during the reporting period, other
than those covered by generic or
measure-specific exclusions.
Number of home health episodes
of care ending with a discharge
during the reporting period, other
than those covered by generic or
measure-specific exclusions.
Number of home health episodes
of care ending with discharge or
transfer to inpatient facility during
the reporting period, other than
those covered by generic or
measure-specific exclusions.
Number of home health stays that
begin during the 12-month observation period. A home health
stay is a sequence of home
health payment episodes separated from other home health
payment episodes by at least 60
days.
Number of home health stays that
begin during the 12-month observation period. A home health
stay is a sequence of home
health payment episodes separated from other home health
payment episodes by at least 60
days.
Number of home health episodes
of care ending with a discharge
during the reporting period, other
than those covered by generic or
measure-specific exclusions.
Number of home health episodes
of care ending with a discharge
during the reporting period, other
than those covered by generic or
measure-specific exclusions.
Number of home health episodes
of care ending with discharge, or
transfer to inpatient facility during
the reporting period, other than
those covered by generic or
measure-specific exclusions.
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TABLE 15—MEASURE SET FOR THE HHVBP MODEL* BEGINNING PY 3—Continued
Measure title
Measure type
Identifier
Data source
Numerator
Patient & Caregiver-Centered
Experience.
Population/Community Health.
NQS domains
Willingness to
recommend the
agency.
Influenza Vaccination Coverage for Home
Health Care
Personnel.
Outcome .......
.......................
CAHPS .........
NA ...................................................
NA.
Process .........
NQF0431
(Used in
other care
settings, not
Home
Health).
Reported by
HHAs
through
Web Portal.
Number of healthcare personnel
who
are
working
in
the
healthcare facility for at least 1
working day between October 1
and March 31 of the following
year, regardless of clinical responsibility or patient contact.
Population/Community Health.
Herpes zoster
(Shingles) vaccination: Has
the patient ever
received the
shingles vaccination?
Advance Care
Plan.
Process .........
NA .................
Reported by
HHAs
through
Web Portal.
Healthcare personnel in the denominator population who during
the time from October 1 (or when
the vaccine became available)
through March 31 of the following
year: a) received an influenza
vaccination administered at the
healthcare facility, or reported in
writing or provided documentation that influenza vaccination
was received elsewhere: or b)
were determined to have a medical contraindication/condition of
severe allergic reaction to eggs
or to other components of the
vaccine or history of GuillainBarre Syndrome within 6 weeks
after a previous influenza vaccination; or c) declined influenza
vaccination; or d) persons with
unknown vaccination status or
who do not otherwise meet any
of the definitions of the abovementioned numerator categories.
Total number of Medicare beneficiaries aged 60 years and over
who report having ever received
zoster vaccine (shingles vaccine).
Process .........
NQF0326 ......
Reported by
HHAs
through
Web Portal.
Patients who have an advance
care plan or surrogate decision
maker documented in the medical record or documentation in
the medical record that an advanced care plan was discussed
but the patient did not wish or
was not able to name a surrogate decision maker or provide
an advance care plan.
All patients aged 65 years and
older.
Communication &
Care Coordination.
Denominator
Total number of Medicare beneficiaries aged 60 years and over
receiving services from the HHA.
* Notes: For more detailed information on the measures utilizing OASIS refer to the OASIS–C1/ICD–9, Changed Items & Data Collection Resources dated September 3, 2014 available at www.oasisanswers.com/LiteratureRetrieve.aspx?ID=215074. For NQF endorsed measures see The NQF Quality Positioning System
available at https://www.qualityforum.org/QPS. For non-NQF measures using OASIS see links for data tables related to OASIS measures at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html. For information on HHCAHPS measures see https://
homehealthcahps.org/SurveyandProtocols/SurveyMaterials.aspx.
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C. Quality Measures for Future
Consideration
The CY 2016 HH PPS final rule
discusses the HHVBP Model design, the
guiding principles to select measures,
and the six priority areas of the National
Quality Strategy (NQS) we considered
for the Model (80 FR 68656 through
68678). Under the HHVBP Model, any
measures we determine to be good
indicators of quality will be considered
for use in the HHVBP Model in future
years, and may be added or removed
through the rulemaking process. To
further our commitment to objectively
assess HHVBP quality measures, we are
utilizing an implementation contractor
that invited a group of measure experts
to provide advice on the adjustment of
the current measure set for
consideration. The contractor convened
a technical expert panel (TEP)
consisting of 11 panelists with expertise
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in home health care and quality
measures that met on September 7,
2016, in Baltimore, Maryland and via
conference call on December 2, 2016.
The TEP discussed developing a
composite total change in ADL/IADL
measure; a composite functional decline
measure; a measure to capture when an
HHA correctly identifies the patient’s
need for mental and behavioral health
supervision; and a measure to identify
if a caregiver is able to provide the
patient’s mental or behavioral health
supervision, to align with
§ 409.45(b)(3)(iii) and the Medicare
Benefit Policy Manual (Pub. 100–02),
Chapter 7, Section 20.2. We discussed
each of these potential measures in
further detail in the CY 2018 HH PPS
proposed rule (82 FR 35336 through
35340), and also discuss in this section
of this final rule. While any new
measures would be proposed for use in
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future rulemaking, we solicited
comment on these potential measures
now to inform measure development
and selection.
As noted in the CY 2017 HH PPS final
rule (81 FR 76747), we received several
comments expressing concern that the
measures under the Model do not reflect
the patient population served under the
Medicare Home Health benefit as the
outcome measures focus on a patient’s
clinical improvement and do not
address patients with chronic illnesses;
deteriorating neurological, pulmonary,
cardiac, and other conditions; and some
with terminal illness. The commenters
opined that the value of including
stabilization measures in the HHVBP
Model is readily apparent as it aligns
the Model with the Medicare Home
Health benefit. Commenters also
expressed concerns that improvement is
not always the goal for each patient and
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Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
1. Total Change in ADL/IADL
Performance by HHA Patients
The measure set finalized in the CY
2016 HH PPS final rule included
Change in Daily Activity Function as
Measured by the Activity Measure for
Post-Acute Care (AM–PAC) (NQF
#0430). However, the measure was
removed in the CY 2017 HH PPS final
rule and never used in the HHVBP
Model because the measure required use
of a proprietary data collection
instrument in the home health
environment. We stated in the CY 2018
HH PPS proposed rule that we were
considering replacing Change in Daily
Activity Function as Measured by AM–
PAC (NQF #0430) with a composite
total ADL/IADL change performance
measure. During the September 2016
TEP meeting, an alternative to the
Change in Daily Activity Function
measure was presented. The TEP
requested that a composite Total ADL/
IADL Change measure be investigated
empirically. This measure was
discussed as part of the follow-up
conference call, and the TEP supported
continued development of the measure
in the HHVBP Model as a way of
including a measure that captures all
three potential outcomes for home
health patients: stabilization; decline;
and improvement. They provided input
on the technical specifications of the
potential composite measure, including
the feasibility of implementing the
measure and the overall measure
reliability and validity. We noted in the
CY 2018 HH PPS proposed rule that we
reviewed this suggested alternative and
believe this measure would provide
actionable and transparent information
that would support HHA efforts to
improve care and prevent functional
decline for all patients across a broad
range of patient functional outcomes.
The measure would also improve
accountability during an episode of care
when the patient is directly under the
HHA’s care.
We noted in the CY 2018 HH PPS
proposed rule that the name of this
potential composite measure could be
Total Change in ADL/IADL Performance
by HHA Patients. The measure would
report the average, normalized, total
improved functioning across the 11
ADL/IADL items on the current OASIS–
C2 instrument. The measure is
calculated by comparing scores from the
start-of-care/resumption of care to
scores at discharge. For each item the
patient’s discharge assessed
performance score is subtracted from
the patient’s start of care/resumption of
care assessed performance score, and
then divided by the maximum
improvement value based on the
number of response options for that
item. These values are summed into a
total normalized change score that can
range from ¥11 (that is, for an episode
where there is maximum decline on all
11 items used in the measure) to +11
(that is, for an episode where there is
the maximum improvement on all 11
items). An HHA’s score on the measure
is based on its average across all eligible
episodes. Patients who are independent
on all 11 ADL/IADL items at Start of
Care (SOC)/Resumption of Care (ROC)
would also be included in the measure.
The HHA’s observed score on the
measure is the average of the
normalized total scores for all eligible
episodes for its patients during the
reporting period.
The following 11 ADLs/IADL-related
items from OASIS–C2 items were
included in developing a composite
measure:
ADL OASIS–C2 items related to SelfCare:
• M1800 (Grooming).
• M1810 (Upper body dressing).
• M1820 (Lower body dressing).
• M1845 (Toileting hygiene).
• M1870 (Eating).
ADL OASIS–C2 items related to
Mobility:
• M1840 (Toilet transferring).
• M1840 (Bed transferring).
17 Fox, John (1997). Applied Regression Analysis,
Linear Models, and Related\Methods/Edition 1,
1997, SAGE.
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• M1860 (Ambulation).
Other IADLs OASIS items:
• M1880 (Light meal preparation).
• M1890 (Telephone use).
• M2020 (Oral medication
management).
Based on these identified measures,
we would risk-adjust using OASIS–C2
items to account for case-mix variation
and other factors that affect functional
decline but are outside the influence of
the HHA. The risk-adjustment model
uses an ordinary least squares (OLS) 17 18
regression framework because the
outcome measure (normalized change in
ADL/IADL performance) is a continuous
variable.
The prediction model for this
outcome measure was derived using the
predicted values from the 11 individual
outcomes that are currently used to risk
adjust these 11 individual quality
measures. Of the 11 values tested, the 8
identified in the proposed rule were
found to be statistically related to the
Total Change in ADL/IADL Performance
by HHA Patients measure at p < 0.0001
level and would be used in the
prediction model that we are
considering proposing to use to risk
adjust the HHA’s observed value for this
potential future measure. The prediction
model for this outcome measure uses
predicted values from the following
individual outcomes (NOTE: The primary
source OASIS item is listed in
parenthesis after the name of the quality
measure):
• Improvement in Upper Body
Dressing (M1810).
• Improvement in Management of
Oral Medications (M2020).
• Improvement in Bed Transferring
(M1850).
• Improvement in Ambulation/
Locomotion (M1860).
• Improvement in Grooming (M1800).
• Improvement in Toileting Hygiene
(M1845).
• Discharged to the Community
(M2420).
• Improvement in Toileting Transfer
(M1840).
Two predictive models, one based on
predicted values from CY 2014 and one
from CY 2015, were computed. The
correlations at the episode level
between observed and predicted values
for the target outcome measure Total
Change in ADL/IADL Performance by
HHA Patients are shown in Table 16.
18 Greene, William H. (2017). Econometric
analysis (8th ed.). New Jersey: Pearson. ISBN 978–
0134461366.
that stabilization is a reasonable clinical
goal for some patients. Commenters
suggested the addition of stabilization or
maintenance measures be considered for
the HHVBP Model. Many commenters
objected to the use of improvement
measures in the HHVBP Model. We did
not receive any specific measures for
future consideration as part of those
comments. In the CY 2018 HH PPS
proposed rule (82 FR 35336 through
35340), we identified measures that we
are considering for possible inclusion
under the Model in future rulemaking
and sought input from the public on the
measures described, as well as any
input about the development or
construction of the measures and their
features or methodologies. We are also
including the description of these
possible measures in this final rule in
the subsections that follow.
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Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
TABLE 16—CORRELATIONS AT THE EPISODE LEVEL BETWEEN OBSERVED AND PREDICTED VALUES FOR THE TARGET
OUTCOME MEASURE TOTAL CHANGE IN ADL/IADL PERFORMANCE BY HHA PATIENTS
Data group
CY2014,
CY2014,
CY2015,
CY2015,
National .........................................................................................................................
HHVBP states ...............................................................................................................
National .........................................................................................................................
HHVBP states ...............................................................................................................
The results in Table 16 suggest that
either model would account for 25
percent or more of the variability in the
outcome measure. These models could
be considered very strong predictive
models for the target outcome measure.
Although the analysis supports
developing a composite measure, the
analysis assumes that the OASIS–C2
items identified to be used in the
composite measure do not change.
However, we recognize that OASIS–C2
items could be removed or added in any
given year. We expect to conduct an
additional analysis, in advance of any
future proposal, to assess whether
changes to OASIS–C2 items that are
removed or added could significantly
impact a HHA’s ability to address
several measures to improve its overall
score in the composite measure. We
solicited public comments on whether
or not to include a composite total ADL/
IADL change performance measure in
the set of applicable measures, the name
of any such measure, the risk
adjustment method, and whether we
should conduct an analysis of the
impact of removal/addition of OASIS–
C2 items.
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Correlation
2. Composite Functional Decline
Measure
The second measure we are
considering for possible inclusion under
the Model in future rulemaking is a
Composite Functional Decline Measure
that could be the percentage of episodes
where there was decline on one or more
of the eight ADL items used in the
measure. As noted in the CY 2018 HH
PPS proposed rule and this final rule,
we received comments on the CY 2017
HH PPS proposed rule suggesting that
we consider the addition of stabilization
or maintenance measures. We stated in
the CY 2018 HH PPS proposed rule that
to address this suggestion, we are
considering a composite functional
decline measure because the existing
functional stabilization measures, taken
individually, are topped out, with HHA
level means of 95 percent or higher.
This type of composite functional
decline measure is similar to the
composite ADL decline measure that is
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used in the Skilled Nursing Facility
(SNF) Quality Reporting program
(QRP).19 The SNF QRP measure is
constructed from four ADL items: Bed
mobility; transfer; eating; and toileting.
An HHVBP composite functional
decline measure could provide
actionable and transparent information
that could support HHA efforts to
improve care and prevent functional
decline for all patients, including those
for whom improvement in functional
status is not a realistic care goal. We
noted in the CY 2018 HH PPS proposed
rule that this concept was discussed
during the TEP meeting on September 7,
2016, with a follow-up conference call
held on December 2, 2016. The TEP
supported the inclusion of measures of
stabilization and decline in the HHVBP
Model, as well as further development
of the composite functional decline
measure. They provided input on the
technical specifications of the potential
composite measure, including the
feasibility of implementing the measure
and the overall measure reliability and
validity.
When calculating the composite
functional decline measure, we noted
that we could use the following 8
existing OASIS–C2 items:
• Ambulation/Locomotion (M1860).
• Bed Transferring (M1840).
• Toilet Transferring (M1840).
• Bathing (M1830).
• Toilet Hygiene (M1845).
• Lower Body Dressing (M1820).
• Upper Body Dressing (M1810).
• Grooming (M1800).
We noted that the measure could be
defined as 1 if there is decline reported
in one or more of these items between
the Start of Care and the Discharge
assessments and zero if no decline is
reported on any of these items. As with
other OASIS-based measures, a
performance score for the measure
would only be calculated for HHAs that
have 20 or more episodes of care during
a performance year.
19 ‘‘Long-stay Nursing Home Care: Percent of
Residents Whose Need for help with Activities of
Daily Living has Increased.’’ https://
www.qualitymeasures.ahrq.gov/summaries/
summary/50060.
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0.5022
0.5094
0.5011
0.5076
Significance
(p < )
0.0001
0.0001
0.0001
0.0001
r2 (Coeff.
Determination)
%
25.22
25.95
25.11
25.76
The measure could be risk-adjusted
using OASIS–C2 items to account for
case-mix variation and other factors that
affect functional decline but are outside
of the influence of the HHA. The riskadjustment model uses a logistic
regression framework. The model
includes a large number of patient
clinical conditions and other
characteristics measured at start of care.
A logistic regression model is estimated
to predict whether the patient will have
a length of stay of greater than 60 days.
The predicted probability of a length of
stay of greater than 60 days is used,
along with other patient characteristics,
to construct a logistic regression model
to predict the probability of decline in
any of eight ADLs. This model is used
to estimate the predicted percent of ADL
decline at the HHA level. To calculate
case-mix adjusted values, the observed
value of the measure is adjusted by the
difference between the HHA predicted
percent and the national predicted
percent. The risk-adjustment model
reduces the adjusted difference between
HHAs that serve a disproportionate
number of longer-stay patients and
those that serve patients with more
typical lengths of stay of one episode.
Across all participating HHAs in the
HHVBP Model, for HHAs that had less
than 20 percent of episodes lasting more
than 60 days, the average on the
functional decline measure was 8.08
percent. This increased to 11.08 percent
for HHAs with 20 percent to 40 percent
of episodes lasting more than 60 days,
14.23 percent for HHAs with 40 percent
to 60 percent of episodes lasting more
than 60 days, and 20.59 percent for
HHAs with more than 60 percent of
episodes lasting more than 60 days. This
finding suggests that, in addition to
focusing on prevention of functional
decline, we should also attempt to better
predict a patient’s functional trajectory
and potentially stratify the population
to exclude those on a likely downward
trajectory. However, in spite of this
finding, the inclusion of a measure that
rewards providers for avoiding
functional decline has the advantage of
diversifying the set of measures for the
HHVBP model. We solicited public
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comments on whether or not to include
a composite functional decline measure
in the set of applicable measures, the
name of any such measure, the risk
adjustment method, and whether we
should conduct an analysis of the
impact of removal/addition of OASIS–
C2 items.
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3. Behavioral Health Measures
Although we did not receive
comments or suggestions through the
rulemaking process for the HHVBP
Model regarding behavioral or mental
health measures, we noted in the CY
2018 HH PPS proposed rule that we
recognize that the Model does not
include such measures. The OASIS–C2
collects several items related to
behavioral and mental health (M1700
Cognitive Functioning; M1710
Confusion Frequency; M1720 Anxiety;
M1730 Depression Screening; M1740
Cognitive, Behavioral, and Psychiatric
Symptoms; M1745 Frequency of
Disruptive Behavior Symptoms; and
M1750 Psychiatric Nursing Services).
These items are used to compute both
Improvement and Process measures as
well as Potentially Avoidable Events.
The inclusion of behavioral health
measures is important for care
transformation and improvement
activities as many persons served by the
Home Health program may have
behavioral health needs.
The TEP made several suggestions
during the December 2016 conference
call as to whether the focus of a
behavioral or mental health measure
could be identifying whether a patient
needed mental or behavioral health
assistance compared to the supervision
of the patient or advocacy assistance.
The TEP supported the supervision type
measure due to its opportunity for
potential improvement. In further
analyses, we identified two underlying
components to outcomes for providing
assistance. We developed a method,
described in the following section, to
identify patients who have or do not
have needs for mental or behavioral
health supervision. We noted that we
are considering further refining this
method by identifying the involvement
of the caregiver in addressing the
patient’s mental or behavioral health
supervision needs as an important
outcome measure, and we solicited
comment on whether this is an
appropriate factor or feature that we
should consider in developing such a
measure in future rulemaking.
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a. HHA Correctly Identifies Patient’s
Need for Mental or Behavioral Health
Supervision
We stated in the CY 2018 HH PPS
proposed rule that we are considering
adding a HHA Correctly Identifies
Patient’s Need for Mental or Behavioral
Health Supervision measure to the
HHVBP Model in the future to capture
a patient’s need for mental or behavioral
health supervision based on an
identifier. This identifier is based on
information from existing Neuro/
Emotional/Behavioral Status OASIS
items, along with other indicators of
mental/behavioral health problems to
identify a patient in need of supervisory
assistance. The outcome measure
assesses whether the HHA correctly
identifies whether or not the patient
needs mental or behavioral health
supervision based on the OASIS SOC/
ROC assessment item M2102f, Types
and Sources of Assistance: Supervision
and Safety.
A composite Mental/Behavioral
Health measure could be a dichotomous
measure that reports the percentage of
episodes of care where the HHA
correctly identifies: (a) Patients who
need mental or behavioral health
supervision; and (b) patients who do not
need mental or behavioral health
supervision. The numerator could be a
combination of two values: (1) The
number of episodes of care where the
HHA correctly identifies patients who
need mental or behavioral health
supervision; plus (2) the number of
episodes of care where the HHA
correctly identifies patients who do not
need mental or behavioral health
supervision. The denominator is all
episodes of care.
The composite measure requires that
a patient’s need for mental or behavioral
health supervision be identified. The
following algorithm was designed to
identify if a patient was in need of
mental or behavioral health supervision.
If the patient met any of the following
conditions, the patient was identified by
the algorithm as in need of mental or
behavioral health supervision:
• Was discharged from a psychiatric
hospital prior to entering home health
care (M1000 = 6).
• Is diagnosed as having chronic
mental behavioral problems (M1021 and
M1023).
• Is diagnosed with a mental illness
(M1021 and M1023).
• Is cognitively impaired (M1700 ≥ 2).
• Is confused (M1710 ≥ 2).
• Is identified as having a memory
deficit (M1740 = 1).
• Is identified as having impaired
decision-making (M1740 = 2).
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• Is identified as being verbally
disruptive (M1740 = 3).
• Is identified as being physically
aggressive (M1740 = 4).
• Is identified as exhibiting
disruptive, infantile, or inappropriate
behaviors (M1740 = 5).
• Is identified as being delusional
(M1740 = 6).
• Has a frequency of disruptive
symptoms (M1745 ≥ 2).
The measure also requires that the
HHA identify if the patient is in need of
mental or behavioral health supervision.
This requirement is based on the SOC/
ROC code for M2102f, Types and
Sources of Assistance: Supervision and
Safety. If the HHA codes a value of zero,
then the HHA has identified this patient
as not needing mental or behavioral
health supervision. If the HHA codes
another value for M2102f, Types and
Sources of Assistance: Supervision and
Safety, then the HHA has identified this
patient as needing mental or behavioral
health supervision. The outcome
measure is defined as the agreement
between the algorithm’s identification of
a patient’s need for mental or behavioral
health supervision and the HHA’s
coding of this need. That is, if—
• The algorithm identifies the patient
as not in need of mental or behavioral
health supervision and the HHA
identifies the patient as not in need of
mental or behavioral health supervision;
or
• The algorithm identifies the patient
as in need of mental or behavioral
health supervision and the HHA
identifies the patient as in need of
mental or behavioral health supervision;
then
• The outcome is coded as 1,
successful.
As with other OASIS-based measures,
a performance score for the measure
would only be calculated for HHAs that
have 20 or more episodes of care during
a performance year.
The measure is risk-adjusted using
OASIS–C2 items to account for case-mix
variation and other factors that affect
functional decline but are outside the
influence of the HHA. The riskadjustment model uses a logistic
regression framework. The model
includes a large number of patient
clinical conditions and other
characteristics measured at the start of
care. To calculate case-mix adjusted
values, the observed value of the
measure is adjusted by the difference
between the HHA predicted percent and
the national predicted percent.
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The prediction model for this
outcome measure uses 39 risk factors 20
with each risk factor statistically
significant at p<0.0001. The correlation
for the model between observed and
predicted values as estimated by
Somers’ D 21 is 0.427, that yields an
estimated coefficient of determination
(r2) value based on the Tau-a 22 of 0.201.
This suggests that the variability in the
model accounts for (predicts)
approximately 20 percent of the
variability in the outcome measure. The
best statistic for evaluating the power of
a prediction model that is derived using
logistic regression is the c-statistic.23
This statistic identifies the overall
accuracy of prediction by comparing
observed and predicted value pairs to
the proportion of the time that both
predict the outcome in the same
direction with 0.500 being a coin-flip.
The discussed prediction model has a cstatistic equal to 0.713, which is
considered to be good. Using data from
CY 2015, the episode-level mean for the
HHA Correctly Identifies Patient’s Need
for Mental or Behavioral Health
Supervision measure is 61.98 percent,
nationally, and 62.98 percent for the
HHVBP states.
20 ‘‘Home Health Quality Initiative: Quality
Measures’’ https://www.cms.gov/Medicare/QualityInitiatives-Patient-Assessment-Instruments/
HomeHealthQualityInits/
HHQIQualityMeasures.html
21 Somers’ D is a statistic that is based on the
concept of concordant vs. discordant pairs for two
related values. In this case, if both the observed and
predicted values are higher than the average or if
both values are less than the average, then the pair
of numbers is considered concordant. However, if
one value is higher than average and the other is
lower than average—or vice versa, then the pair of
values is considered discordant. The Somer’s D is
(# of concordant pairs—# of discordant pairs)/total
# of pairs. The higher the ratio, the stronger the
concordance between the two set of values.
22 The Kendall Tau-a assumes that if there is a
correlation between two variables, then sorting the
variables based on one of the values will result in
ordering the second variable. It uses the same
concept of concordant pairs in Somers’ D but a
different formula: t = [(4P)/[(n) (n–1)]—1 where
p = # of concordant pairs and n = # of pairs. This
correlation method reduces the effect of outlier
values as the values are essentially ranked.
23 The C-statistic (sometimes called the
‘‘concordance’’ statistic or C-index) is a measure of
goodness of fit for binary outcomes in a logistic
regression model. In clinical studies, the C-statistic
gives the probability a randomly selected patient
who experienced an event (for example, a disease
or condition) had a higher risk score than a patient
who had not experienced the event. It is equal to
the area under the Receiver Operating Characteristic
(ROC) curve and ranges from 0.5 to 1.
• A value below 0.5 indicates a very poor model.
• A value of 0.5 means that the model is no better
than predicting an outcome than random chance.
• Values over 0.7 indicate a good model.
• Values over 0.8 indicate a strong model.
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b. Caregiver Can/Does Provide for
Patient’s Mental or Behavioral Health
Supervision Need
We stated in the CY 2018 HH PPS
proposed rule that we are considering
including under the Model in future
rulemaking a Caregiver Can/Does
Provide for Patient’s Mental or
Behavioral Health Supervision Need
measure that would encourage HHAs to
ensure that patients who need mental or
behavioral health supervision are
receiving such care from the patient’s
caregivers, and would be a realistic care
goal.
When considering how to develop a
measure to determine whether or not
the caregiver can/does provide the
patient’s mental or behavioral health
supervision, we would create an
identifier of a patient’s need for mental
or behavioral health supervision. This
identifier is based on the same
algorithm described in the previous
section from existing Neuro/Emotional/
Behavioral Status OASIS items along
with other indicators of mental/
behavioral health problems to identify a
patient in need of supervisory
assistance. The outcome measure is
whether the HHA correctly identifies
this patient as having the need for
mental or behavioral health supervision
based on the OASIS SOC/ROC
assessment item M2102f, Types and
Sources of Assistance: Supervision and
Safety.
The measure could be a dichotomous
measure that reports the percentage of
episodes where patients with identified
mental or behavioral health supervision
needs have their needs met or could
have their needs met by the patient’s
caregiver with additional training (if
needed) and support by the HHA. The
numerator is the intersection of the
number of episodes of care where: (1)
The patient needs mental or behavioral
health supervision; and (2) these
patients have their needs met or could
have their needs met by the patient’s
caregiver with additional training (if
needed) and support by the HHA. By
intersection, we mean that, for the
numerator to equal one, a patient has to
need mental or behavioral health
supervision and has to have these needs
met by his or her caregiver, or could
have their needs met by the caregiver
with additional training and/or support
by the HHA. The denominator is all
episodes of care. The algorithm
discussed previously for HHA Correctly
Identifies Patient’s Need for Mental or
Behavioral Health Supervision could
also be used to first identify if a patient
was in need of mental or behavioral
health supervision.
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To identify whether caregivers are
able to provide supervisory care or, with
training, could be able to provide
supervisory care for these patients, we
could use the SOC/ROC code for
M2102f, Types and Sources of
Assistance: Supervision and Safety. If
the HHA codes a value of 1 (Non-agency
caregiver(s) currently provide
assistance) or 2 (Non-agency caregiver(s)
need training/supportive services to
provide assistance), then the measure
identifies that a caregiver does or could
provide supervision to a patient who
has been identified as needing mental or
behavioral health supervision.
The outcome measure is defined as
the agreement between the algorithm’s
identification of a patient’s need for
mental or behavioral health supervision
and the availability of supervision from
the patient’s caregiver(s). That is, if—
• The algorithm identifies the patient
as in need of mental or behavioral
health supervision and there is
documentation that the patient’s
caregiver(s) do or could provide this
supervision; then
• The outcome is coded as 1,
successful.
As with other OASIS-based measures,
a performance score for the measure
would only be calculated for HHAs that
have 20 or more episodes during a
performance year. We would use the
same methodology to risk-adjust by
using OASIS–C2 items and the
prediction model described previously.
The prediction model for this outcome
measure uses 55 risk factors with each
risk factor significant at p <0.0001. The
correlation for the model between
observed and predicted values as
estimated by Somers’ D is 0.672, that
yields an estimated coefficient of
determination (r2) value based on the
Tau-a of 0.205. This suggests that the
variability in the model accounts for
(predicts) approximately 20 percent of
the variability in the outcome measure.
The best statistic for evaluating the
power of a prediction model that is
derived using logistic regression is the
c-statistic. This statistic identifies the
overall accuracy of prediction by
comparing observed and predicted
value pairs to the proportion of the time
that both predict the outcome in the
same direction with 0.500 being a coinflip. The prediction model has a cstatistic equal to 0.836, which is
considered to be extremely strong.
We noted in the CY 2018 HH PPS
proposed rule that we are considering
whether the HHA Correctly Identifies
Patient’s Need for Mental or Behavioral
Health Supervision measure or the
Caregiver Can/Does Provide for Patient’s
Mental or Behavioral Health
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Supervision Need measure would be
most meaningful to include in the
Model. We also noted that we were
considering the interactions between the
Home Health Grouping Model (HHGM)
proposal on quality measures discussed
in section III. of the proposed rule and
the HHVBP Model for the quality
measures discussed in section IV.B of
the proposed rule. We solicited public
comments on the methodologies,
analyses used to test the quality
measure, and issues described in this
section for future measure
considerations. We noted that we will
continue to share analyses as they
become available with participating
HHAs during future webinars.
The following is a summary of the
public comments received on the
‘‘Quality Measures for Future
Consideration’’ and our responses:
Comment: We received several
comments from stakeholders offering
their input on the quality measures
discussed. Many were receptive to the
development of new measures. Some
commenters supported the development
of composite measures, but believed
improvement should not be the sole
focus of any measure as they indicated
that many patients benefit greatly from
skilled home health services but are not
likely to improve on these measures.
While many commenters were in
support of the inclusion of measures
that capture an agency’s ability to
identify mental or behavioral health
needs and identify whether a caregiver
is available to provide behavioral
supervision, they cautioned CMS that
home health providers should not be
made responsible for determining
behavioral health diagnoses outside of a
simple recognition of need. MedPAC
was one of a few commenters that did
not support developing new process
measures, such as the described
measure concepts of correctly
identifying the patient’s need for mental
and behavioral health supervision, and
identifying if a caregiver is able to
provide the patient’s mental or
behavioral health supervision. MedPAC
indicated that while it believes that
improving a patient’s functional ability
is a goal of home health care, it has
some degree of concern that the
‘composite total change in ADL/IADL
measure’ and the ‘composite functional
decline measure’ represent reporting
elements completely within the control
of the home health agency. MedPAC
recommended that if CMS includes
these measures, it may also want to
consider and propose ways that such
data could be independently audited or
otherwise verified. Another commenter
opposed the addition of a composite
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functional decline measure as they
believe it rewards agencies that have
selective admission practices of refusing
patients that are likely to decline toward
end of life, and also opposed the
inclusion of behavioral health measures
as they believe that they may discourage
agencies from accepting patients when
there are behavioral health issues or few
local resources.
Response: We appreciate the
comments on the discussion of the
measures that we are considering for
possible inclusion in the Model and will
take the recommendations into
consideration as we determine whether
or not to include new measures in
future rulemaking.
Comment: In response to our
solicitation of public comment, we also
received a few comments that were
outside the scope of discussion of the
specific future quality measures that we
are considering, as discussed in the
proposed rule. A commenter
recommended that CMS develop and
implement HHVBP policies in
alignment with Congressional activity
supporting one national approach to
VBP for home care services. Another
commenter recommended that CMS
factor quality metrics into HHVBP that
not only relate to health outcomes, but
also that are within the control of the
home health care provider, adequately
measuring the quality of care provided.
Another commenter recommended that
CMS ensure that value-based home
health purchasing models incorporate a
shared definition of value that
incorporates the patient and caregiver
voice. A few commenters questioned the
level of payment at risk under the
Model, and believed that placing up to
eight percent of HHA payment at risk
for performance is too much. A few
commenters questioned the geographic
participation criteria for the Model and
recommended including voluntary
participation by interested HHAs in
non-participating states.
Response: We appreciate the
comment to align home health VBP
policies with Congressional activity
supporting a national approach to VBP
home care services. We also appreciate
the comments that recommend
adequately measuring the quality of care
provided and for CMS to ensure that
value-based home health purchasing
models incorporate a shared definition
of value that incorporates the patient
and caregiver voice. As an Innovation
Center model, we are closely monitoring
the quality measures and will address
any needed adjustments through future
rulemaking. With respect to the
comments regarding the level of
payment at risk under the Model, as
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discussed in the CY 2016 HH PPS final
rule (80 FR 68687), competing HHAs
that provide the highest quality of care
and that receive the maximum upward
adjustment will improve their financial
viability that could ensure that the
vulnerable population that they serve
has access to high quality care. Only
HHAs that provide very poor quality of
care, relative to the cohort they compete
within, would be subject to the highest
downward payment adjustments. We
appreciate the desire for interested
HHAs in non-participating states to
participate in the Model, but do not
plan to re-open the Model to additional
participants at this time.
We appreciate the comments on
potential new quality measures and
intend to continue to provide
opportunities for stakeholder input as
we consider additional measures for
possible inclusion in the HHVBP
Model’s applicable measure set. We will
continue to collect and analyze data as
we consider whether to propose any
additional measures in future
rulemaking.
V. Updates to the Home Health Care
Quality Reporting Program (HH QRP)
A. Background and Statutory Authority
Section 1895(b)(3)(B)(v)(II) of the Act
requires that for 2007 and subsequent
years, each HHA submit to the Secretary
in a form and manner, and at a time,
specified by the Secretary, such data
that the Secretary determines are
appropriate for the measurement of
health care quality. To the extent that an
HHA does not submit data in
accordance with this clause, the
Secretary is directed to reduce the home
health market basket percentage
increase applicable to the HHA for such
year by 2 percentage points. As
provided at section 1895(b)(3)(B)(vi) of
the Act, depending on the market basket
percentage increase applicable for a
particular year, the reduction of that
increase by 2 percentage points for
failure to comply with the requirements
of the HH QRP and (except in 2018)
further reduction of the increase by the
productivity adjustment described in
section 1886(b)(3)(B)(xi)(II) of the Act
may result in the home health market
basket percentage increase being less
than 0.0 percent for a year, and may
result in payment rates under the Home
Health PPS for a year being less than
payment rates for the preceding year.
We use the terminology ‘‘CY [year]
HH QRP’’ to refer to the calendar year
for which the HH QRP requirements
applicable to that calendar year must be
met in order for an HHA to avoid a 2
percentage point reduction to its market
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basket percentage increase under
section 1895(b)(3)(B)(v)(I) of the Act
when calculating the payment rates
applicable to it for that calendar year.
The Improving Medicare Post-Acute
Care Transformation Act of 2014 (Pub.
L. 113–185, enacted on October 6, 2014)
(IMPACT Act) amended Title XVIII of
the Act, in part, by adding new section
1899B of the Act, entitled
‘‘Standardized Post-Acute Care
Assessment Data for Quality, Payment,
and Discharge Planning,’’ and by
enacting new data reporting
requirements for certain post-acute care
(PAC) providers, including Home
Health Agencies (HHAs). Specifically,
new sections 1899B(a)(1)(A)(ii) and (iii)
of the Act require HHAs, Inpatient
Rehabilitation Facilities (IRFs), Long
Term Care Hospitals (LTCHs) and
Skilled Nursing Facilities (SNFs), under
each of their respective quality reporting
program (which, for HHAs, is found at
section 1895(b)(3)(B)(v) of the Act), to
report data on quality measures
specified under section 1899B(c)(1) of
the Act for at least five domains, and
data on resource use and other measures
specified under section 1899B(d)(1) of
the Act for at least three domains.
Section 1899B(a)(1)(A)(i) of the Act
further requires each of these PAC
providers to report under its respective
quality reporting program standardized
patient assessment data in accordance
with subsection (b) for at least the
quality measures specified under
subsection (c)(1) and that is with respect
to five specific categories: Functional
status; cognitive function and mental
status; special services, treatments, and
interventions; medical conditions and
co-morbidities; and impairments. All of
the data that must be reported in
accordance with section 1899B(a)(1)(A)
of the Act must be standardized and
interoperable, so as to allow for the
exchange of the information among PAC
providers and other providers, as well
as for the use of such data to enable
access to longitudinal information and
to facilitate coordinated care. We refer
readers to the CY 2016 HH PPS final
rule (80 FR 68690 through 68692) for
additional information on the IMPACT
Act and its applicability to HHAs.
B. General Considerations Used for the
Selection of Quality Measures for the
HH QRP
We refer readers to the CY 2016 HH
PPS final rule (80 FR 68695 through
68698) for a detailed discussion of the
considerations we apply in measure
selection for the HH QRP, such as
alignment with the CMS Quality
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Strategy,24 which incorporates the three
broad aims of the National Quality
Strategy.25 As part of our consideration
for measures for use in the HH QRP, we
review and evaluate measures that have
been implemented in other programs
and take into account measures that
have been endorsed by NQF for
provider settings other than the home
health setting. We have previously
adopted measures with the term
‘‘Application of’’ in the names of those
measures. We have received questions
pertaining to the term ‘‘application’’ and
clarified in the proposed rule that when
we refer to a measure as an
‘‘Application of’’ the measure, we mean
that the measure would be used in a
setting other than the setting for which
it was endorsed by the NQF. For
example, in the FY 2016 SNF PPS Rule
(80 FR 46440 through 46444) we
adopted An Application of the Measure
Percent of Residents with Experiencing
Falls with Major Injury (Long Stay)
(NQF #0674), which is endorsed for the
Nursing Home setting but not the SNF
setting. For such measures, we stated
that we intend to seek NQF
endorsement for the home health
setting, and if the NQF endorses one or
more of them, we would update the title
of the measure to remove the reference
to ‘‘Application of.’’
We received comments on the
considerations we apply in our measure
selection and on other topics related to
measures used in the HH QRP.
Comment: Some commenters
supported the standardization of
measures and data across HHAs, LTCHs,
IRFs, and SNFs so that CMS can make
comparisons between them, but
cautioned that such standardization
could compromise the validity of the
data. These commenters stated that the
home is different than institutional
settings because the patient has a greater
role in determining how, when, and if
certain interventions are provided, and
that individual skill, cognitive and
functional ability, and financial
resources affect the ability of home
health patients to safely manage their
health care needs, interventions, and
medication regimens. Other commenters
expressed concerns about the reliability
and validity of cross-setting measures
due to the unique characteristics of the
home health setting and emphasized
caution in interpreting measure rates.
Response: We appreciate the support
for standardization to enable
24 https://www.cms.gov/Medicare/QualityInitiatives-Patient-Assessment-Instruments/
QualityInitiativesGenInfo/CMS-QualityStrategy.html.
25 https://www.ahrq.gov/workingforquality/nqs/
nqs2011annlrpt.htm.
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comparisons across post-acute care
providers. We also recognize the
uniqueness of the home setting,
including patients’ capacity to directly
and independently manage their
environment and health care needs,
such as medications and treatments.
However, we disagree that patients are
limited in their freedom to help set their
goals and preferences when receiving
care services within LTCHs, IRFs or
SNFs. In our measure development and
alignment work, we continuously assess
and account for the unique
characteristics of home health patients
including the use of risk-adjustment
models that account for differences in
cognitive and functional ability.
Further, we are mindful that regardless
of where services are rendered, risk
adjustment is generally applied to
characteristics of the individual rather
than the provider setting.
All of the measures we proposed to
adopt for the HH QRP were tested for
reliability and/or validity, and we
believe that the results of that testing
support our conclusion that the
measures are sufficiently reliable and
valid to warrant their adoption in the
HH QRP. The results of our reliability
and validity testing for these measures
may be found in the Measure
Specifications for Measures Proposed in
CY 2018 HH QRP Final Rule, posted on
the CMS HH QRP Web page at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HHQIQualityMeasures.html. We will
continue to test, monitor and validate
these measures as part of measure
maintenance.
Comment: One commenter suggested
that the claims-based measures be
weighted more than OASIS measures in
order to control for inflated outcomes.
Another commenter was concerned that
OASIS measure data can be
manipulated and suggested the HH QRP
should only use claims-based measures
because they are more objective.
Response: We wish to clarify that we
do not weight home health measures in
the home health quality reporting
program. However, we believe that the
commenter is concerned about the
gaming on behalf of home health
agencies. We believe that the collection
of both claims-based and OASIS based
measures is appropriate for the program.
Claims-based data can be limited
because they are associated with billing
and do not always provide a complete
picture of the patient’s health
assessment status. OASIS fills in those
gaps by giving us additional information
about care processes and outcomes that
are furnished to HHA patients.
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Although we recognize that OASIS
assessments are, by their nature, more
subjective than claims, we require
HHAs to attest to the accuracy of the
data submitted on each OASIS
assessment.
C. Accounting for Social Risk Factors in
the HH QRP
In the CY 2018 HH PPS proposed rule
(82 FR 35341 through 35342), we
discussed accounting for social risk
factors in the HH QRP. We understand
that social risk factors such as income,
education, race and ethnicity,
employment, disability, community
resources, and social support (certain
factors of which are also sometimes
referred to as socioeconomic status
(SES) factors or socio-demographic
status (SDS) factors) play a major role in
health. One of our core objectives is to
improve beneficiary outcomes including
reducing health disparities, and we
want to ensure that all beneficiaries,
including those with social risk factors,
receive high quality care. In addition,
we seek to ensure that the quality of
care furnished by providers and
suppliers is assessed as fairly as
possible under our programs while
ensuring that beneficiaries have
adequate access to excellent care.
We have been reviewing reports
prepared by the Office of the Assistant
Secretary for Planning and Evaluation
(ASPE 26) and the National Academies
of Sciences, Engineering, and Medicine
on the issue of measuring and
accounting for social risk factors in
CMS’ quality measurement and
payment programs, and considering
options on how to address the issue in
these programs. On December 21, 2016,
ASPE submitted a Report to Congress on
a study it was required to conduct under
section 2(d) of the Improving Medicare
Post-Acute Care Transformation
(IMPACT) Act of 2014. The study
analyzed the effects of certain social risk
factors of Medicare beneficiaries on
quality measures and measures of
resource use used in one or more of nine
Medicare value-based purchasing
programs.27 The report also included
considerations for strategies to account
for social risk factors in these programs.
In a January 10, 2017 report released by
The National Academies of Sciences,
Engineering, and Medicine, that body
provided various potential methods for
26 https://aspe.hhs.gov/pdf-report/reportcongress-social-risk-factors-and-performanceunder-medicares-value-based-purchasingprograms.
27 https://aspe.hhs.gov/pdf-report/reportcongress-social-risk-factors-and-performanceunder-medicares-value-based-purchasingprograms.
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measuring and accounting for social risk
factors, including stratified public
reporting.28
In addition, the NQF undertook a 2year trial period in which new
measures, measures undergoing
maintenance review, and measures
endorsed with the condition that they
enter the trial period were assessed to
determine whether risk adjustment for
selected social risk factors was
appropriate for these measures.
Measures from the HH QRP,
Rehospitalization During the First 30
Days of Home Health (NQF# 2380), and
Emergency Department Use without
Hospital Readmission During the First
30 Days of Home Health (NQF# 2505)
were included in this trial. This trial
entailed temporarily allowing inclusion
of social risk factors in the riskadjustment approach for these
measures. Since the publication of the
CY 2018 HH PPS proposed rule, the
National Quality Forum (NQF) has
concluded their initial trial on risk
adjustment for quality measures. Based
on the findings from the initial trial,
NQF will continue its work to evaluate
the impact of social risk factor
adjustment on intermediate outcome
and outcome measures for an additional
3 years. The extension of this work will
allow NQF to determine further how to
effectively account for social risk factors
through risk adjustment and other
strategies in quality measurement.
As we continue to consider the
analyses and recommendations from
these reports, we are continuing to work
with stakeholders in this process. As we
have previously communicated, we are
concerned about holding providers to
different standards for the outcomes of
their patients with social risk factors
because we do not want to mask
potential disparities or minimize
incentives to improve the outcomes for
disadvantaged populations. Keeping
this concern in mind, while we sought
input on this topic previously, we
continue to seek public comment on
whether we should account for social
risk factors in measures in the HH QRP,
and if so, what method or combination
of methods would be most appropriate
for accounting for social risk factors.
Examples of methods include:
confidential reporting to providers of
measure rates stratified by social risk
factors, public reporting of stratified
measure rates, and potential risk
adjustment of a particular measure as
appropriate based on data and evidence.
28 National Academies of Sciences, Engineering,
and Medicine. 2017. Accounting for social risk
factors in Medicare payment. Washington, DC: The
National Academies Press.
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In addition, in the CY 2018 HH PPS
proposed rule (82 FR 35341 through
35342), we sought public comment on
which social risk factors might be most
appropriate for reporting stratified
measure scores and potential risk
adjustment of a particular measure.
Examples of social risk factors include,
but are not limited to, dual eligibility/
low-income subsidy, race and ethnicity,
and geographic area of residence. We
also sought comments on which of these
factors, including current data sources
where this information would be
available, could be used alone or in
combination, and whether other data
should be collected to better capture the
effects of social risk. We will take
commenters’ input into consideration as
we continue to assess the
appropriateness and feasibility of
accounting for social risk factors in the
HH QRP. We note that to the extent we
consider making any changes we would
propose them through future notice and
comment rulemaking.
We look forward to working with
stakeholders as we consider the issue of
accounting for social risk factors and
reducing health disparities in CMS
programs. Of note, implementing any of
the methods previously stated will be
taken into consideration in the context
of how this and other CMS programs
operate (for example, data submission
methods, availability of data, statistical
considerations relating to reliability of
data calculations, among others), so we
also sought comment on operational
considerations. We are committed to
ensuring that beneficiaries have access
to and receive excellent care, and that
the quality of care furnished by
providers and suppliers is assessed
fairly in CMS programs. This section of
this final rule includes a discussion of
the comments we received on this topic,
along with our responses.
Comment: Commenters were
generally supportive of accounting for
social risk factors in the HH QRP quality
measures. Many commenters stated that
there was evidence demonstrating that
these factors can have substantial
influence on patient health outcomes.
Some commenters who supported
accounting for social risk factors noted
that these factors are outside the control
of the provider and were concerned that
without risk adjustment, differences in
quality scores may reflect differences in
patient populations rather than
differences in quality.
A few other commenters, while
acknowledging the influence of social
risk factors on health outcomes,
cautioned against adjusting for them in
quality measurement due to the
potential for unintended consequences.
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These commenters expressed concern
over the possibility that risk- adjusted
measures may remove incentives for
quality improvement among facilities
that serve higher levels of underserved
populations.
Regarding risk adjustment
methodology, some commenters made
specific recommendations regarding the
type of risk adjustment that must be
used. Commenters stated that any risk
stratification must be considered on a
measure-by-measure basis, and that
measures that are broadly within the
control of the provider and reflective of
direct care, such as pressure ulcers,
must not be stratified. The commenters
stated that social risk factor adjustment
be used only on outcome measures, not
process measures. One commenter
alternately suggested using
socioeconomic factors to stratify, rather
than adjust, measure results. Multiple
commenters recommended that we
conduct further research and testing of
risk-adjustment methods. A commenter
suggested that CMS use Social Risk
Factors, Social Determinants of Health
or Distressed Communities Index scores
within the HH QRP. Some commenters
suggested the formation of a TEP to
further refine the use of such data.
In addition to supporting race and
ethnicity, dual eligibility status, and
geographical location, commenters
suggested additional risk factors,
including: Patient-level factors such as
lack of personal resources, education
level, and employment. Some
commenters also suggested community
resources and other factors such as
access to adequate food, medications,
living conditions (including living
alone), and lack of an adequate support
system or caregiver availability. Several
encouraged the development of
measures that reflect person-centered
domains to improve the focus on
outcomes for disadvantaged
populations.
A few commenters provided feedback
on confidential and public reporting of
data adjusted for social risk factors. A
commenter suggested that CMS start
with confidential reporting and, once
there has been opportunity for HHAs to
review and understand their results,
CMS could transition to public
reporting.
Response: We thank commenters for
their suggestions. As we have
previously stated, we are concerned
about holding providers to different
standards for the outcomes of their
patients with social risk factors because
we do not want to mask potential
disparities. We believe that the path
forward must incentivize improvements
in health outcomes for disadvantaged
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populations while ensuring that
beneficiaries have adequate access to
excellent care. Also, based on the
findings from the initial trial, NQF will
continue its work to evaluate the impact
of social risk factor adjustment on
intermediate outcome and outcome
measures for an additional three years.
The extension of this work will allow
NQF to determine further how to
effectively account for social risk factors
through risk adjustment and other
strategies in quality measurement. We
await recommendations of the NQF trial
to further inform our efforts.
We will consider all suggestions as we
continue to assess each measure and the
overall HH QRP. We intend to explore
options including but not limited to
measure stratification by social risk
factors in a consistent manner across
several quality reporting programs,
informed by considerations of
stratification methods described in
IX.A.13 of the preamble of the FY 2018
IPPS/LTCH PPS final rule. We thank
commenters for this important feedback
and will continue to consider options to
account for social risk factors that will
allow us to address disparities and
potentially incentivize improvement in
care for patients and beneficiaries. We
will also consider providing feedback to
providers on outcomes for individuals
with social risk factors in confidential
reports.
D. Removal of OASIS Items
In the CY 2018 HH PPS proposed rule
(82 FR 35342) we proposed to remove
247 data elements from 35 OASIS items
collected at specific time points during
a home health episode. These data
elements are not used in the calculation
of quality measures already adopted in
the HH QRP, nor are they being used for
previously established purposes
unrelated to the HH QRP, including
payment, survey, the HH VBP Model or
care planning. We included list of the
35 OASIS items we proposed to remove,
in part or in their entirety, in Table 45
of the proposed rule (82 FR 35342 and
35343) and also made them available at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
OASIS-Data-Sets.html. Subsequent to
issuing the proposed rule, we
discovered that we had inadvertently
included three OASIS items in Table 45
that are used either for payment or for
the HH QRP. Those items are M1200
Vision (used for payment), M2030
Management of Injectable Medications
(used for payment), and M1730
Depression Screening (used in the HH
QRP). Accordingly, we will not be
removing these items from the OASIS.
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Comment: Many commenters
supported our proposal to remove items
from OASIS. Most of these commenters
agreed that items not used for the
purposes of determining patient
outcomes or the quality of care should
be removed.
Response: We appreciate the support
for our proposal to remove items from
OASIS.
Comment: One commenter noted that
OASIS Item M2250 (Plan of Care
Synopsis) is proposed for removal and
questioned whether OASIS Item M2401
(Intervention Synopsis) will continue to
be collected.
Response: We proposed to remove
OASIS Item M2250 because it is not
used for the HH QRP or for any other
purpose. OASIS Item M2401 is used in
the calculation of the quality measure
Diabetic Foot Care and Patient
Education Implemented (NQF #0519),
which we adopted in the CY 2010 HH
PPS final rule (74 FR 58096), and will
therefore continue to be collected at the
time point of Transfer to an Inpatient
Facility and Discharge from Agency.
Comment: One commenter questioned
if there is another OASIS version that
will be implemented so that a
beneficiary’s Medicare Beneficiary
Identifier (MBI) can be provided in the
OASIS.
Response: Effective January 1, 2018
the OASIS–C2 will be able to
accommodate the MBI which is an
alternative Medicare Beneficiary
Identifier that we are adopting to
replace the Social Security number
(SSN)-based Health Insurance Claim
Number (HICN) in an effort to prevent
identity theft in the Medicare
population. Instructions for reporting
OASIS Item M0063 (Medicare
Beneficiary Number) can be found in
the OASIS–C2 Guidance Manual:
Effective January 1, 2018 at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
Downloads/OASIS-C2-GuidanceManual-Effective_1_1_18.pdf.
Comment: A few commenters raised
concerns about the overall burden
associated with CMS’ proposals, noting
that if all proposed new assessment
items are finalized, the new assessment
items could be more burdensome to
collect than the one being removed.
Response: We appreciate the
comments and as more fully discussed
in section V.H. of this final rule, we
have decided not to finalize the
standardized patient assessment data
elements proposed for three of the five
categories under § 1899B(b)(1)(B) of the
Act: Cognitive Function and Mental
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Status; Special Services, Treatments,
and Interventions; and Impairments.
Final Decision: After consideration of
the comments received, we are
finalizing the removal of 235 data
elements from 33 OASIS items collected
at specific time points during a home
health episode, effective with all HHA
assessments on or after January 1, 2019.
As previously explained, we will
continue to collect OASIS items M1200,
M2030 and M1730. Table 17 lists the
51715
OASIS items and data elements to be
removed and they can also be found at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
OASIS-Data-Sets.html.
TABLE 17—ITEMS TO BE REMOVED FROM OASIS EFFECTIVE JANUARY 1, 2019
Specific time point
OASIS item
Start of care
Resumption of
care
Follow-up
Transfer to
an inpatient
facility
Death at
home
Discharge
from agency
M0903 ......................................................
M1011 ......................................................
M1017 ......................................................
M1018 ......................................................
M1025 ......................................................
M1034 ......................................................
M1036 ......................................................
M1210 ......................................................
M1220 ......................................................
M1230 ......................................................
M1240 ......................................................
M1300 ......................................................
M1302 ......................................................
M1320 ......................................................
M1322 ......................................................
M1332 ......................................................
M1350 ......................................................
M1410 ......................................................
M1501 ......................................................
M1511 ......................................................
M1610 ......................................................
M1615 ......................................................
M1750 ......................................................
M1880 ......................................................
M1890 ......................................................
M1900 ......................................................
M2030 ......................................................
M2040 ......................................................
M2102 * ....................................................
M2110 ......................................................
M2250 ......................................................
M2310 ......................................................
M2430 ......................................................
........................
6
6
6
12
1
4
1
1
1
1
1
1
1
........................
........................
1
3
........................
........................
........................
1
1
1
1
4
........................
2
6
1
7
........................
........................
........................
6
6
6
12
1
4
1
1
1
1
1
1
1
........................
........................
1
3
........................
........................
........................
1
1
1
1
4
........................
2
6
1
7
........................
........................
........................
6
........................
........................
12
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
1
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
1
5
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
*** 15
20
1
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
........................
1
........................
........................
........................
........................
........................
........................
........................
........................
1
........................
........................
........................
1
1
1
........................
........................
1
5
1
1
........................
1
1
........................
1
........................
** 3
........................
........................
*** 15
........................
Total ..................................................
70
70
18
42
1
34
* M2102 row f to remain collected at Start of Care, Resumption of Care and Discharge from Agency as part of the HH VBP program.
** M2102 rows a, c, d to remain collected at Discharge from Agency for survey purposes.
*** M2310 responses 1, 10, OTH, UK to remain collected at Transfer to an Inpatient Facility and Discharge from Agency for survey purposes.
E. Collection of Standardized Patient
Assessment Data Under the HH QRP
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1. Definition of Standardized Patient
Assessment Data
Section 1895(b)(3)(B)(v)(IV)(bb) of the
Act requires that beginning with the CY
2019 HH QRP, HHAs report
standardized patient assessment data
required under section 1899B(b)(1) of
the Act. For purposes of meeting this
requirement, section
1895(b)(3)(B)(v)(IV)(cc) of the Act
requires that a HHA submit the
standardized patient assessment data
required under section 1899B(b)(1) of
the Act in the form and manner, and at
the time, as specified by the Secretary.
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Section 1899B(b)(1)(B) of the Act
describes standardized patient
assessment data as data required for at
least the quality measures described in
sections 1899B(c)(1) of the Act and that
is with respect to the following
categories:
• Functional status, such as mobility
and self-care at admission to a PAC
provider and before discharge from a
PAC provider.
• Cognitive function, such as ability
to express and understand ideas, and
mental status, such as depression and
dementia.
• Special services, treatments and
interventions such as the need for
ventilator use, dialysis, chemotherapy,
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central line placement, and total
parenteral nutrition.
• Medical conditions and
comorbidities such as diabetes,
congestive heart failure and pressure
ulcers.
• Impairments, such as incontinence
and an impaired ability to hear, see or
swallow.
• Other categories deemed necessary
and appropriate by the Secretary.
As required under section
1899B(b)(1)(A) of the Act, the
standardized patient assessment data
must be reported at least for the
beginning of the home health episode
(for example, HH start of care/
resumption of care) and end of episode
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(discharge), but the Secretary may
require the data to be reported more
frequently.
In the CY 2018 HH PPS proposed rule
(82 FR 35343), we proposed to define
the standardized patient assessment
data that HHAs must report under the
HH QRP, as well as the requirements for
the reporting of these data. The
collection of standardized patient
assessment data is critical to our efforts
to drive improvement in healthcare
quality across the four post-acute care
(PAC) settings to which the IMPACT
Act applies. We noted that we intend to
use these data for a number of purposes,
including facilitating their exchange and
longitudinal use among healthcare
providers to enable high quality care
and outcomes through care
coordination, as well as for quality
measure calculation, and identifying
comorbidities that might increase the
medical complexity of a particular
admission.
HHAs are currently required to report
patient assessment data through the
Outcome and Assessment Information
Set (OASIS) by responding to an
identical set of assessment questions
using an identical set of response
options (we refer to a solitary question/
response option as a data element and
we refer to a group of questions/
responses as data elements), both of
which incorporate an identical set of
definitions and standards. The primary
purpose of the identical questions and
response options is to ensure that we
collect a set of standardized data
elements across HHAs, which we can
then use for a number of purposes,
including HH payment and measure
calculation for the HH QRP.
LTCHs, IRFs, and SNFs are also
required to report patient assessment
data through their applicable PAC
assessment instruments, and they do so
by responding to identical assessment
questions developed for their respective
settings using an identical set of
response options (which incorporate an
identical set of definitions and
standards). Like the OASIS, the
questions and response options for each
of these other PAC assessment
instruments are standardized across the
PAC provider type to which the PAC
assessment instrument applies.
However, the assessment questions and
response options in the four PAC
assessment instruments are not
currently standardized with each other.
As a result, questions and response
options that appear on the OASIS
cannot be readily compared with
questions and response options that
appear, for example, on the Inpatient
Rehabilitation Facility-Patient
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Assessment Instrument (IRF–PAI),
which is the PAC assessment
instrument used by IRFs. This is true
even when the questions and response
options are similar. This lack of
standardization across the four PAC
provider types has limited our ability to
compare one PAC provider type with
another for purposes such as care
coordination and quality improvement.
To achieve a level of standardization
across HHAs, LTCHs, IRFs, and SNFs
that enables us to make comparisons
between them, we proposed to define
‘‘standardized patient assessment data’’
as patient or resident assessment
questions and response options that are
identical in all four PAC assessment
instruments, and to which identical
standards and definitions apply.
We stated in the proposed rule that
standardizing the questions and
response options across the four PAC
assessment instruments is an essential
step in making that data interoperable,
allowing it to be shared electronically,
or otherwise, between PAC provider
types. It will enable the data to be
comparable for various purposes,
including the development of crosssetting quality measures and to inform
payment models that take into account
patient characteristics rather than
setting, as described in the IMPACT Act.
We did not receive any specific
comments on the proposed definition.
Final Decision: We are finalizing as
proposed our definition of standardized
patient assessment data.
2. General Considerations Used for the
Selection of Standardized Patient
Assessment Data
As part of our effort to identify
appropriate standardized patient
assessment data for purposes of
collecting under the HH QRP, we sought
input from the general public,
stakeholder community, and subject
matter experts on items that would
enable person-centered, high quality
health care, as well as access to
longitudinal information to facilitate
coordinated care and improved
beneficiary outcomes.
To identify optimal data elements for
standardization, our data element
contractor organized teams of
researchers for each category, with each
team working with a group of advisors
made up of clinicians and academic
researchers with expertise in PAC.
Information-gathering activities were
used to identify data elements, as well
as key themes related to the categories
described in section 1899B(b)(1)(B) of
the Act. In January and February 2016,
our data element contractor also
conducted provider focus groups for
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each of the four PAC provider types,
and a focus group for consumers that
included current or former PAC patients
and residents, caregivers, ombudsmen,
and patient advocacy group
representatives. The Development and
Maintenance of Post-Acute Care CrossSetting Standardized Patient
Assessment Data Focus Group Summary
Report is available at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Post-Acute-Care-QualityInitiatives/IMPACT-Act-of-2014/
IMPACT-Act-Downloads-andVideos.html.
Our data element contractor also
assembled a 16-member TEP that met on
April 7 and 8, 2016, and January 5 and
6, 2017, in Baltimore, Maryland, to
provide expert input on data elements
that are currently in each PAC
assessment instrument, as well as data
elements that could be standardized.
The Development and Maintenance of
Post-Acute Care Cross-Setting
Standardized Patient Assessment Data
TEP Summary Reports are available at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Post-Acute-Care-QualityInitiatives/IMPACT-Act-of-2014/
IMPACT-Act-Downloads-andVideos.html.
As part of the environmental scan,
data elements currently in the four
existing PAC assessment instruments
were examined to see if any could be
considered for proposal as standardized
patient assessment data. Specifically,
this evaluation included consideration
of data elements in OASIS–C2 (effective
January 2017); IRF–PAI, v1.4 (effective
October 2016); LCDS, v3.00 (effective
April 2016); and MDS 3.0, v1.14
(effective October 2016). Data elements
in the standardized assessment
instrument that we tested in the PostAcute Care Payment Reform
Demonstration (PAC PRD)—the
Continuity Assessment Record and
public reporting Evaluation (CARE)—
were also considered. A literature
search was also conducted to determine
whether we could propose to adopt
additional data elements as
standardized patient assessment data.
Additionally, we held four Special
Open Door Forums (SODFs) on October
27, 2015; May 12, 2016; September 15,
2016; and December 8, 2016, to present
data elements we were considering and
to solicit input. At each SODF, some
stakeholders provided immediate input,
and all were invited to submit
additional comments via the CMS
IMPACT Mailbox:
PACQualityInitiative@cms.hhs.gov.
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We also convened a meeting with
federal agency subject matter experts
(SMEs) on May 13, 2016. In addition, a
public comment period was open from
August 12 to September 12, 2016 to
solicit comments on detailed candidate
data element descriptions, data
collection methods, and coding
methods. The IMPACT Act Public
Comment Summary Report containing
the public comments (summarized and
verbatim) and our responses is available
at https://www.cms.gov/Medicare/
Quality-Initiatives-Patient-AssessmentInstruments/Post-Acute-Care-QualityInitiatives/IMPACT-Act-of-2014/
IMPACT-Act-Downloads-andVideos.html.
We specifically sought to identify
standardized patient assessment data
that we could feasibly incorporate into
the LTCH, IRF, SNF, and HHA
assessment instruments and that have
the following attributes: (1) Being
supported by current science; (2) testing
well in terms of their reliability and
validity, consistent with findings from
the Post-Acute Care Payment Reform
Demonstration (PAC PRD); (3) the
potential to be shared (for example,
through interoperable means) among
PAC and other provider types to
facilitate efficient care coordination and
improved beneficiary outcomes; (4) the
potential to inform the development of
quality, resource use and other
measures, as well as future payment
methodologies that could more directly
take into account individual beneficiary
health characteristics; and (5) the ability
to be used by practitioners to inform
their clinical decision and care planning
activities. We also applied the same
considerations that we apply to quality
measures, including the CMS Quality
Strategy which is framed using the three
broad aims of the National Quality
Strategy.
3. Policy for Retaining HH QRP
Measures and Standardized Patient
Assessment Data
In the CY 2017 HH PPS final rule (81
FR 76755 through 76756), we adopted a
policy that will allow for any quality
measure adopted for use in the HH QRP
to remain in effect until the measure is
removed, suspended, or replaced. For
further information on how measures
are considered for removal, suspension
or replacement, we refer readers to the
CY 2017 HH PPS final rule (81 FR 76755
through 76756). We proposed to apply
this same policy to the standardized
patient assessment data that we adopt
for the HH QRP.
Comment: Several commenters
supported this proposal.
Response: We appreciate the
commenters’ support.
Final Decision: We are finalizing that
our policy for retaining HH QRP
measures will apply to the standardized
patient assessment data that we adopt
for the HH QRP.
4. Policy for Adopting Changes to HH
QRP Measures and Application of That
Policy to Standardized Patient
Assessment Data
In the CY 2017 HH PPS final rule (81
FR 76756), we adopted a subregulatory
process to incorporate updates to HH
quality measure specifications that do
not substantively change the nature of
the measure. We noted that substantive
changes will be proposed and finalized
through rulemaking. For further
information on what constitutes a
substantive versus a nonsubstantive
change and the subregulatory process
51717
for nonsubstantive changes, we refer
readers to the CY 2017 HH PPS final
rule (81 FR 76756). We proposed to
apply this policy to the standardized
patient assessment data that we adopt
for the HH QRP. We invited public
comment on this proposal.
Comment: One commenter requested
that we propose to adopt all substantive
changes to measures only after soliciting
input from a technical expert panel of
home health clinical leaders, holding a
Special Open Door Forum to explain the
changes under consideration, and
allowing stakeholders to submit
meaningful comments on those
potential changes.
Response: We agree that input from
both technical experts and the public is
critical to the measure development
process, and we generally solicit both
types of input when we consider
whether to propose substantive updates
to measures. We also solicit input in
other ways, such as through open door
forums and solicitations for public
comment, and often engage in these
activities prior to proposing substantive
updates through the rulemaking
process. Finally, the rulemaking process
itself gives the public an additional
opportunity to comment on the
substantive updates to measures under
consideration.
Final Decision: After consideration of
the public comments, we are finalizing
that we will apply our policy for
adopting changes to HH QRP measures
to the standardized patient assessment
data that we adopt for the HH QRP.
5. Quality Measures Previously
Finalized for the HH QRP
The HH QRP currently has 23
measures, as outlined in Table 18.
TABLE 18—MEASURES CURRENTLY ADOPTED FOR THE HH QRP
Short name
Measure name & data source
OASIS-based
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Pressure Ulcers ...........................................
DRR .............................................................
Ambulation ...................................................
Bathing .........................................................
Dyspnea .......................................................
Oral Medications ..........................................
Pain ..............................................................
Surgical Wounds ..........................................
Bed Transferring ..........................................
Timely Care ..................................................
Depression Assessment ..............................
Influenza .......................................................
PPV ..............................................................
Falls Risk .....................................................
Diabetic Foot Care .......................................
Drug Education ............................................
Percent of Patients or Residents with Pressure Ulcers that are New or Worsened (NQF # 0678).* ∂
Drug Regimen Review Conducted with Follow-Up for Identified Issues-Post Acute Care (PAC) Home Health Quality Reporting Program.∂
Improvement in Ambulation/Locomotion (NQF #0167).
Improvement in Bathing (NQF #0174).
Improvement in Dyspnea.
Improvement in Management of Oral Medication (NQF #0176).
Improvement in Pain Interfering with Activity (NQF #0177).
Improvement in Status of Surgical Wounds (NQF #0178).
Improvement in Bed Transferring (NQF # 0175).
Timely Initiation Of Care (NQF # 0526).
Depression Assessment Conducted.
Influenza Immunization Received for Current Flu Season (NQF #0522).
Pneumococcal Polysaccharide Vaccine Ever Received (NQF #0525).
Multifactor Fall Risk Assessment Conducted For All Patients Who Can Ambulate (NQF #0537).
Diabetic Foot Care and Patient/Caregiver Education Implemented during All Episodes of Care (NQF #0519).
Drug Education on All Medications Provided to Patient/Caregiver during All Episodes of Care.
Claims-based
MSPB ...........................................................
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Total Estimated Medicare Spending Per Beneficiary (MSPB)—Post Acute Care (PAC) Home Health (HH) Quality Reporting Program (QRP). ∂
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TABLE 18—MEASURES CURRENTLY ADOPTED FOR THE HH QRP—Continued
Short name
Measure name & data source
DTC ..............................................................
PPR ..............................................................
ACH ..............................................................
ED Use .........................................................
Rehospitalization ..........................................
ED Use without Readmission ......................
Discharge to Community-Post Acute Care (PAC) Home Health (HH) Quality Reporting Program (QRP). ∂
Potentially Preventable 30-Day Post-Discharge Readmission Measure for Home Health Quality Reporting Program. ∂
Acute Care Hospitalization During the First 60 Days of Home Health (NQF #0171).
Emergency Department Use without Hospitalization During the First 60 Days of Home Health (NQF #0173).
Rehospitalization During the First 30 Days of Home Health (NQF #2380).
Emergency Department Use without Hospital Readmission During the First 30 Days of Home Health (NQF #2505).
HHCAHPs-based
Professional Care ........................................
Communication ............................................
Team Discussion .........................................
Overall Rating ..............................................
Willing to Recommend .................................
How often the home health team gave care in a professional way.
How well did the home health team communicate with patients.
Did the home health team discuss medicines, pain, and home safety with patients.
How do patients rate the overall care from the home health agency.
Will patients recommend the home health agency to friends and family.
* Not currently NQF-endorsed for the home health setting.
The data collection period will begin with CY 2017 Q1&2 reporting for CY 2018 APU determination, followed by the previously established HH QRP use of 12
months (July 1, 2017–June 30, 2018) of CY 2017 reporting for CY 2019 APU determination. Subsequent years will be based on the HH July 1–June 30 timeframe for
APU purposes. For claims data, the performance period will use rolling CY claims for subsequent reporting purposes.
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F. New HH QRP Quality Measures
Beginning With the CY 2020 HH QRP
In the CY 2018 HH PPS proposed rule
(82 FR 35345) we proposed that
beginning with the CY 2020 HH QRP, in
addition to the quality measures we are
retaining under our policy described in
section V.B. of this final rule, we would
replace the current pressure ulcer
measure entitled Percent of Residents or
Patients with Pressure Ulcers That Are
New or Worsened (Short Stay) (NQF
#0678) with a modified version of the
measure and adopt one measure on
patient falls and one measure on
assessment of patient functional status.
We also proposed to characterize the
data elements described in this section
as standardized patient assessment data
under section 1899B(b)(1)(B) of the Act
that must be reported by HHAs under
the HH QRP through the OASIS. The
new measures that we proposed to
adopt are as follows:
• Changes in Skin Integrity PostAcute Care: Pressure Ulcer/Injury.
• Application of Percent of Residents
Experiencing One or More Falls with
Major Injury (NQF #0674).
• Application of Percent of LongTerm Care Hospital Patients with an
Admission and Discharge Functional
Assessment and a Care Plan That
Addresses Function (NQF #2631).
The measures are described in more
detail as follows:
1. Replacing the Current Pressure Ulcer
Quality Measure, Entitled Percent of
Residents or Patients With Pressure
Ulcers That Are New or Worsened
(Short Stay) (NQF #0678), With a
Modified Pressure Ulcer Measure,
Entitled Changes in Skin Integrity PostAcute Care: Pressure Ulcer/Injury
a. Measure Background
We proposed to remove the current
pressure ulcer measure, Percent of
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Residents or Patients with Pressure
Ulcers That Are New or Worsened
(Short Stay) (NQF #0678), from the HH
QRP measure set and to replace it with
a modified version of that measure,
Changes in Skin Integrity Post-Acute
Care: Pressure Ulcer/Injury, beginning
with the CY 2020 HH QRP. The change
in the measure name is to reduce
confusion about the new modified
measure. The modified version differs
from the current version of the measure
because it includes new or worsened
unstageable pressure ulcers, including
deep tissue injuries (DTIs), in the
measure numerator. The proposed
modified version of the measure also
contained updated specifications
intended to eliminate redundancies in
the assessment items needed for its
calculation and to reduce the potential
for underestimating the frequency of
pressure ulcers. The modified version of
the measure would satisfy the IMPACT
Act domain of ‘‘Skin integrity and
changes in skin integrity.’’
b. Measure Importance
As described in the CY 2016 HH PPS
final rule (80 FR 68697), pressure ulcers
are high-cost adverse events and are an
important measure of quality. For
information on the history and rationale
for the relevance, importance, and
applicability of having a pressure ulcer
measure in the HH QRP, we referred
readers to the CY 2016 HH PPS final
rule (80 FR 68697 to 68700.
We proposed to adopt a modified
version of the current pressure ulcer
measure because unstageable pressure
ulcers, including DTIs, are similar to
Stage 2, Stage 3, and Stage 4 pressure
ulcers in that they represent poor
outcomes, are a serious medical
condition that can result in death and
disability, are debilitating and painful
and are often an avoidable outcome of
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medical care.29 30 31 32 33 34 Studies show
that most pressure ulcers can be avoided
and can also be healed in acute, postacute, and long term care settings with
appropriate medical care. 35
Furthermore, some studies indicate that
DTIs, if managed using appropriate care,
can be resolved without deteriorating
into a worsened pressure ulcer.36 37
While there are few studies that
provide information regarding the
incidence of unstageable pressure ulcers
in PAC settings, an analysis conducted
by our measure development contractor
indicated that adding unstageable
pressure ulcers to the quality measure
numerator would result in a higher
29 Casey, G. (2013). ‘‘Pressure ulcers reflect
quality of nursing care.’’ Nurs N Z 19(10): 20–24.
30 Gorzoni, M.L. and S.L. Pires (2011). ‘‘Deaths in
nursing homes.’’ Rev Assoc Med Bras 57(3): 327–
331.
31 Thomas, J.M., et al. (2013). ‘‘Systematic review:
health-related characteristics of elderly hospitalized
adults and nursing home residents associated with
short-term mortality.’’ J Am Geriatr Soc 61(6): 902–
911.
32 White-Chu, E.F., et al. (2011). ‘‘Pressure ulcers
in long-term care.’’ Clin Geriatr Med 27(2): 241–258.
33 Bates-Jensen BM. Quality indicators for
prevention and management of pressure ulcers in
vulnerable elders. Ann Int Med. 2001;135 (8 Part 2),
744–51.
34 Bennet, G, Dealy, C Posnett, J (2004). The cost
of pressure ulcers in the UK, Age and Aging,
33(3):230–235.
35 Black, Joyce M., et al. ‘‘Pressure ulcers:
avoidable or unavoidable? Results of the national
pressure ulcer advisory panel consensus
conference.’’ Ostomy-Wound Management 57.2
(2011): 24.
36 Sullivan, R. (2013). A Two-year Retrospective
Review of Suspected Deep Tissue Injury Evolution
in Adult Acute Care Patients. Ostomy Wound
Management 59(9) https://www.o-wm.com/article/
two-year-retrospective-review-suspected-deeptissue-injury-evolution-adult-acute-care-patien.
37 Posthauer, ME, Zulkowski, K. (2005). Special to
OWM: The NPUAP Dual Mission Conference:
Reaching Consensus on Staging and Deep Tissue
Injury. Ostomy Wound Management 51(4) https://
www.o-wm.com/content/the-npuap-dual-missionconference-reaching-consensus-staging-and-deeptissue-injury.
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percentage of patients with new or
worsened pressure ulcers in HHA
settings and increase the variability of
measure scores. A higher percentage
indicates lower quality. This increased
variability serves to improve the
measure by improving the ability of the
measure to distinguish between high
and low quality home health agencies.
We have found in the testing of this
measure that given the low prevalence
of pressure ulcers in the home health
setting, the addition of unstageable
ulcers to this measure could enhance
variability. Analysis of 2015 OASIS data
found that in approximately 1.2 percent,
or more than 70,000 episodes, of
patients had an unstageable ulcer upon
admission. Patients in more than 13,000
episodes were discharged with an
unstageable ulcer. In addition,
unstageable ulcers due to slough/eschar
worsened between admission and
discharge in approximately 5,000
episodes of care. In conclusion, the
inclusion of unstageable pressure ulcers,
including DTIs, in the numerator of this
measure is expected to increase measure
scores and variability in measure scores,
thereby improving the ability to
discriminate among poor- and highperforming HHAs.
Testing shows similar results in other
PAC settings. For example, in SNFs,
using data from Quarter 4 2015 through
Quarter 3 2016, the mean score on the
currently implemented pressure ulcer
measure is 1.75 percent, compared with
2.58 percent in the proposed measure.
In the proposed measure, the SNF mean
score is 2.58 percent; the 25th and 75th
percentiles are 0.65 percent and 3.70
percent, respectively; and 20.32 percent
of facilities have perfect scores. In
LTCHs, using data from Quarter 1
through Quarter 4 2015, the mean score
on the currently implemented pressure
ulcer measure is 1.95 percent, compared
with 3.73 percent in the proposed
measure. In the proposed measure, the
LTCH mean score is 3.73 percent; the
25th and 75th percentiles are 1.53
percent and 4.89 percent, respectively;
and 5.46 percent of facilities have
perfect scores. In IRFs, using data from
Quarter 4 2016, the mean score on the
currently implemented pressure ulcer
measure is 0.64 percent, compared with
1.46 percent in the proposed measure.
In the proposed measure, the IRF mean
score is 1.46 percent and the 25th and
75th percentiles are 0 percent and 2.27
percent, respectively. The inclusion of
unstageable pressure ulcers, including
DTIs, in the numerator of this measure
is expected to increase measure scores
and variability in measure scores,
thereby improving the ability to
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distinguish between poor and high
performing HHAs.
This increased variability of scores
across quarters and deciles may improve
the ability of the measure to distinguish
between high and low performing
providers across PAC settings.
c. Stakeholder Feedback
Our measure development contractor
sought input from subject matter
experts, including Technical Expert
Panels (TEPs), over the course of several
years on various skin integrity topics
and specifically those associated with
the inclusion of unstageable pressure
ulcers including DTIs. Most recently, on
July 18, 2016, a TEP convened by our
measure development contractor
provided input on the technical
specifications of this proposed quality
measure, including the feasibility of
implementing the proposed measure’s
updates across PAC settings. The TEP
supported the use of the proposed
measure across PAC settings, including
the use of different data elements for
measure calculation. The TEP supported
the updates to the measure across PAC
settings, including the inclusion in the
numerator of unstageable pressure
ulcers due to slough and/or eschar that
are new or worsened, new unstageable
pressure ulcers due to a non-removable
dressing or device, and new DTIs. The
TEP recommended supplying additional
guidance to providers regarding each
type of unstageable pressure ulcer. This
support was in agreement with earlier
TEP meetings, held on June 13, and
November 15, 2013, which had
recommended that CMS update the
specifications for the pressure ulcer
measure to include unstageable pressure
ulcers in the numerator.38 39 Exploratory
data analysis conducted by our measure
development contractor suggests that
the addition of unstageable pressure
ulcers, including DTIs, will increase the
38 Schwartz, M., Nguyen, K.H., Swinson Evans,
T.M., Ignaczak, M.K., Thaker, S., and Bernard, S.L.:
Development of a Cross-Setting Quality Measure for
Pressure Ulcers: OY2 Information Gathering, Final
Report. Centers for Medicare & Medicaid Services,
November 2013. Available: https://www.cms.gov/
Medicare/Quality-Initiatives-Patient-AssessmentInstruments/Post-Acute-Care-Quality-Initiatives/
Downloads/Development-of-a-Cross-SettingQuality-Measure-for-Pressure-Ulcers-InformationGathering-Final-Report.pdf.
39 Schwartz, M., Ignaczak, M.K., Swinson Evans,
T.M., Thaker, S., and Smith, L.: The Development
of a Cross-Setting Pressure Ulcer Quality Measure:
Summary Report on November 15, 2013, Technical
Expert Panel Follow-Up Webinar. Centers for
Medicare & Medicaid Services, January 2014.
Available: https://www.cms.gov/Medicare/QualityInitiatives-Patient-Assessment-Instruments/PostAcute-Care-Quality-Initiatives/Downloads/
Development-of-a-Cross-Setting-Pressure-UlcerQuality-Measure-Summary-Report-on-November15-2013-Technical-Expert-Pa.pdf.
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observed incidence of new or worsened
pressure ulcers at the facility level and
may improve the ability of the proposed
quality measure to discriminate between
poor- and high-performing agencies.
We solicited stakeholder feedback on
this proposed measure by means of a
public comment period held from
October 17 through November 17, 2016.
In general, we received considerable
support for the proposed measure. A
few commenters supported all of the
changes to the current pressure ulcer
measure that resulted in the proposed
measure, with one commenter noting
the significance of the work to align the
pressure ulcer quality measure
specifications across the PAC settings.
Many commenters supported the
inclusion of unstageable pressure ulcers
due to slough/eschar, due to nonremovable dressing/device, and DTIs in
the proposed quality measure. Other
commenters did not support the
inclusion of DTIs in the proposed
quality measure because they stated that
there is no universally accepted
definition for this type of skin injury.
Some commenters provided feedback
on the data elements used to calculate
the proposed quality measure. We
believe that these data elements will
promote facilitation of cross-setting
quality comparison as required under
the IMPACT Act, alignment between
quality measures and payment,
reduction in redundancies in
assessment items, and prevention of
inappropriate underestimation of
pressure ulcers. The currently
implemented pressure ulcer measure is
calculated using retrospective data
elements that assess the number of new
or worsened pressure ulcers at each
stage, while the proposed measure is
calculated using data elements that
assess the current number of unhealed
pressure ulcers at each stage, and the
number of these that were present upon
admission, which are subtracted from
the current number at that stage. Some
commenters did not support the data
elements that will be used to calculate
the proposed measure, and requested
further testing of these data elements.
Other commenters supported the use of
these data elements stating that these
data elements simplified the measure
calculation process.
The public comment summary report
for the proposed measure is available on
the CMS Web site at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Post-Acute-Care-QualityInitiatives/IMPACT-Act-of-2014/
IMPACT-Act-Downloads-andVideos.html.
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The NQF-convened Measures
Application Partnership (MAP) PostAcute Care/Long-Term Care (PAC/LTC)
Workgroup met on December 14 and 15,
2016, and provided us input about this
proposed measure. The NQF-convened
MAP PAC/LTC workgroup provided a
recommendation of ‘‘support for
rulemaking’’ for use of the proposed
measure in the HH QRP. The MAP
Coordinating Committee met on January
24 and 25, 2017, and provided a
recommendation of ‘‘conditional
support for rulemaking’’ for use of the
proposed measure in the HH QRP. The
MAP’s conditions of support include
that, as a part of measure
implementation, we provide guidance
on the correct collection and calculation
of the measure result, as well as
guidance on public reporting Web sites
explaining the impact of the
specification changes on the measure
result. The MAP’s conditions also
specify that CMS continue analyzing the
proposed measure to investigate
unexpected results reported in public
comment. We stated in the proposed
rule that we intend to fulfill these
conditions by offering additional
training opportunities and educational
materials in advance of public reporting,
and by continuing to monitor and
analyze the proposed measure. We
currently provide private provider
feedback reports as well as a Quarterly
Quality Measure report that allows
HHAs to track their measure outcomes
for quality improvement purposes.
Aside from those reports, we conduct
internal monitoring and evaluation of
our measures to ensure that the
measures are performing as they were
intended to perform during the
development of the measure. More
information about the MAP’s
recommendations for this measure is
available at https://www.qualityforum.
org/WorkArea/linkit.aspx?Link
Identifier=id&ItemID=84452.
We reviewed the NQF’s consensus
endorsed measures and were unable to
identify any home health measures that
address changes in skin integrity related
to pressure ulcers. Therefore, based on
the evidence previously discussed, we
proposed to adopt the quality measure
entitled, Changes in Skin Integrity PostAcute Care: Pressure Ulcer/Injury, for
the HH QRP beginning with the CY
2020 HH QRP. We noted that we plan
to submit the proposed measure to the
NQF for endorsement consideration as
soon as feasible.
d. Data Collection
The data for this quality measure will
be collected using the OASIS data set,
which is currently submitted by HHAs
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through the Quality Improvement and
Evaluation System (QIES) Assessment
Submission and Processing (ASAP)
System. While the inclusion of
unstageable wounds in the proposed
measure results in a measure calculation
methodology that is different from the
methodology used to calculate the
current pressure ulcer measure, the data
elements needed to calculate the
proposed measure are already included
on the OASIS data set. In addition, our
proposal to eliminate duplicative data
elements that were used in calculation
of the current pressure ulcer measure
will result in an overall reduced
reporting burden for HHAs for the
proposed measure. For more
information on OASIS data set
submission using the QIES ASAP
System, we refer readers to https://
www.qtso.com/.
For technical information about this
proposed measure, including
information about the measure
calculation and the standardized patient
assessment data elements used to
calculate this measure, we refer readers
to the document titled Finalized
Specifications for HH QRP Quality
Measures and Standardized Patient
Assessment Data Elements, available at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HHQIQualityMeasures.html.
We proposed that HHAs will begin
reporting the proposed pressure ulcer
measure, Changes in Skin Integrity PostAcute Care: Pressure Ulcer/Injury,
which will replace the current pressure
ulcer measure, with data collection
beginning with respect to admissions
and discharges occurring on or after
January 1, 2019.
We solicited public comment on our
proposal to remove the current pressure
ulcer measure, Percent of Residents or
Patients with Pressure Ulcers That Are
New or Worsened (Short Stay) (NQF
#0678), and replace it with a modified
version of that measure, entitled,
Changes in Skin Integrity Post-Acute
Care: Pressure Ulcer/Injury, beginning
with the CY 2020 HH QRP.
Comment: Several commenters
supported the proposed replacement of
the current pressure ulcer measure,
Percent of Residents or Patients with
Pressure Ulcers That Are New or
Worsened (Short Stay) (NQF #0678),
with a modified version of that measure
entitled, Changes in Skin Integrity PostAcute Care: Pressure Ulcer/Injury. One
of these commenters noted that this
measure will increase the number of
identified pressure ulcers.
One commenter supported the
proposed measure calculation approach
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because it does not include pressure
ulcers that were present at the time of
admission, and noted that a pressure
ulcer that is present on admission is
only included in the measure if it
subsequently worsens during the home
health episode of care.
Response: We appreciate the
commenters’ support.
Comment: A few commenters
suggested that we make additional
refinements to the proposed measure
before we adopt it for the HH QRP;
however, these commenters did not
specifically describe any proposed
refinements. One commenter stated
generally that the measure was not fully
developed. Another commenter
expressed concerns about the
differences between the specifications
for this measure in the SNF setting
related to other PAC settings, including
the home health setting. A few
commenters additionally commented on
the reliability and validity of the
proposed measure, Changes in Skin
Integrity Post-Acute Care: Pressure
Ulcer/Injury. Some commenters
requested that additional testing
analyses be conducted prior to the
implementation of this measure, and
others recommended that we conduct
additional testing to determine the
applicability of this measure for its use
in the home health setting. One
commenter encouraged CMS to
continue to test the measure to ensure
it collects accurate data.
Response: We believe that the
Changes in Skin Integrity Post-Acute
Care: Pressure Ulcer/Injury measure is a
fully developed measure that is
standardized across the PAC settings,
including in the SNF setting. Testing
results for this measure indicated
increased observed pressure ulcer scores
in the LTCH, IRF, SNF and HH patient
populations when the unstageable
ulcers were included, compared with
the previously implemented pressure
ulcer measure. Specifically, an analysis
conducted by the measure development
contractor, using data from October
through December 2016, showed mean
scores increasing by 2.03 percentage
points in home health, with the addition
of unstageable pressure ulcers in the
measure. The changes in the proposed
measure also increased the variability of
measures scores.
Further, the reliability and validity of
the M0300/M1311 data elements used to
calculate this quality measure have been
tested in several ways. The MDS 3.0
pilot test showed good reliability in the
SNF setting, and we believe that the
results are applicable to other post-acute
care providers, including HHAs,
because the data elements are
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standardized across the LTCH, IRF,
SNF, and HH settings. Testing
conducted to evaluate our ability to
derive the measure’s numerator from the
M0300 data elements revealed that
accuracy improved. The M0300 data
elements are standardized with the
M1311 data elements used in OASIS,
and we are able to determine that we
can also reliably use M1311 data
elements to calculate the measure.
Additionally, with regard to the
reliability of the pressure ulcer data
elements, the average gold-standard to
gold-standard kappa statistic was 0.905.
The average gold-standard to facilitynurse kappa statistic was 0.937. These
kappa scores indicate ‘‘almost perfect’’
agreement using the Landis and Koch
standard for strength of agreement.40
A main difference between the
current and proposed pressure ulcer
measures is that the proposed measure
includes unstageable pressure ulcers,
including DTIs, in the numerator of the
quality measure, resulting in increased
scores in all settings. By including
pressure ulcers that were not included
in the numerator of the current pressure
ulcer measure, the scores on the
proposed measure are higher and the
risk of the measure being ‘‘topped-out’’
is lower.
To assess the construct validity of this
measure, or the degree to which the
measure assesses what it claims or
purports to be assessing, our measure
contractor sought input from TEPs over
the course of several years. Most
recently, on July 18, 2016, a TEP
supported the inclusion in the
numerator of unstageable pressure
ulcers due to slough and/or eschar that
are new or worsened, new unstageable
pressure ulcers/injuries due to a nonremovable dressing or device, and new
DTIs. The measure testing activities
were presented to TEP members for
their input on the reliability, validity,
and feasibility of the proposed measure
and the changes. The TEP members
supported the measure construct.
We intend to continue to perform
reliability and validity testing to ensure
that that the measure demonstrates
scientific acceptability (including
reliability and validity) and meets the
goals of the HH QRP. Further, while we
intend to validate the data collected to
ensure data accuracy, we note that
providers are expected to submit
accurate data. Finally, as with all
measure development and
40 Landis, R., & Koch, G. (1977, March). The
measurement of observer agreement for categorical
data. Biometrics 33(1), 159–174. Landis, R., & Koch,
G. (1977, March). The measurement of observer
agreement for categorical data. Biometrics 33(1),
159–174.
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implementation, we will provide
training and guidance prior to
implementation of the measure to
promote consistency in the
interpretation of the measure.
Comment: A few commenters
suggested that we monitor the measure
for unintended consequences such as
surveillance bias, suggesting that this
could affect measure performance.
Response: We appreciate the
comments pertaining to unintended
consequences, including potential bias
in reporting the number and stage of
pressure ulcers, which could affect
measure performance. We intend to
monitor measure results and item-level
responses on an ongoing basis to
identify potential biases or other issues.
Comment: Some commenters
expressed concerns pertaining to the
importance of appropriate
documentation of unstageable pressure
ulcers, including deep tissue injuries
(DTIs). One commenter commented that
the definition of pressure ulcers
included in the measure may be too
subjective to collect reliable, accurate
measure data across post-acute care
providers, citing DTIs specifically. This
commenter added that, as a result, the
measure could provide misleading
portrayals of HH performance.
Response: We appreciate the
comments pertaining to the concerns
related to appropriate documentation
and definition of unstageable pressure
ulcers. We interpret the commenters’
comment regarding appropriate
documentation of unstageable pressure
ulcers in the medical record to mean
that as a result of this measure,
providers should ensure such
documentation is incorporated into the
medical record. We note that accurate
assessment and documentation of all
patient assessment findings is
customary for ensuring quality care.
We agree that unstageable pressure
ulcers should be appropriately
documented, but disagree that the
definition of pressure ulcers used in the
measure may be too subjective to allow
for accurate and reliable data capture in
post-acute care settings. The definitions
of the pressure-related ulcers and
injuries used in this measure are
standardized and, while all healthcare
assessment information can invoke
clinical subjectivity, we believe that the
definitions provided in our guidance
manuals, which align with nationally
recognized definitions, enables the
collection of data in a reliable manner.
We are also confident, based on the
reliability testing results previously
explained, that the measure can
accurately assess HHA performance.
Further, we intend to provide training to
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HHAs to ensure that they understand
how to properly report it.
Comment: Some commenters
requested training, help desk support,
and guidance in completing the items
that will be used to calculate the
proposed measure. One commenter also
recommended that CMS conduct
training on steps HHAs can take to
improve quality.
Response: We are currently engaged
in efforts to provide educational
activities related to the HH QRP,
including training events and responses
to questions submitted to the Help Desk,
which will include information to help
HHAs understand how to complete and
code the pressure ulcer. Such
educational and training information is
part of our ongoing strategy to ensure
successful implementation of the HH
QRP, and ultimately quality
improvement. Recordings of previous
trainings are available on the CMS
YouTube Web site at https://
www.youtube.com/user/CMSHHSgov/
featured, and we will continue to make
recordings of trainings available there.
We invite HHAs to submit specific
inquiries related to the coding of the
OASIS through our help desk,
HHQualityQuestions@cms.hhs.gov.
Additionally, a Frequently Asked
Questions document is provided
quarterly for the HH QRP, in the
Downloads section of the HH Quality
Reporting FAQs Web site at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HH-Quality-Reporting/HHQuality-Reporting-FAQs-.html. These
FAQ documents are updated to reflect
current guidance related to the HH QRP,
including data submission deadlines
and training materials.
Comment: One commenter noted the
proposed measure requires HHAs to
count the number of unhealed pressure
ulcers at each stage and subtract the
number present upon admission. While
the commenter agreed that excluding
pressure ulcers that are present on
admission is an appropriate
improvement to the measure, the
commenter cautioned that it adds
complexity to the coding process. Other
commenters stated that this information
may be difficult for providers to capture
because of the new data elements used
to calculate the new measure.
Response: We disagree that the
proposed measure will require HHAs to
make adjustments to their coding
processes because HHAs already submit
the data to calculate the modified
measure. Additionally, the assessment
does not require HHAs to tally or count
the number of unhealed pressure ulcers.
We perform that calculation for
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purposes of calculating the measure
rates.
Comment: Several commenters
recommended that CMS attain NQF
endorsement of the Changes in Skin
Integrity Post-Acute Care: Pressure
Ulcer/Injury measure prior to
implementation.
Response: While this measure is not
currently -endorsed by a consensusbased entity, which is currently the
National Quality Forum (NQF), we
believe that this measure possess the
attributes necessary for such
endorsement, including the measure’s
applicability, face validity and
feasibility, and its reliability and
validity as derived from the national
testing. Therefore, we believe that this
measure is appropriate for adoption into
the HH QRP. However, we intend to
submit this measure to NQF for
consideration for its consideration for
endorsement as soon as feasible.
Comment: A few commenters
provided feedback on the use of the
term ‘‘pressure injury’’. Commenters
encouraged CMS to use the terminology
recommended by NPUAP and to align
with their staging definitions, which
will assist providers to be more
standardized.
Response: We have integrated the
current language of NPUAP terminology
for coding the patient and resident
assessment instruments, especially in
light of the recent updates made by the
NPUAP to their Pressure Ulcer Staging
System. The NPUAP announced a
change in terminology to use the term
‘‘pressure injury’’ in April 2016.41 A
TEP held by our measure development
contractor on July 15, 2016, was
supportive of using the term ‘‘pressure
injury.’’ Some members of the TEP
stated that the term ‘‘injury’’ is not
associated with blame or harm by an
entity, that ‘‘injury’’ may be a more
inclusive term than ‘‘ulcer’’, and that
the term ‘‘pressure injury’’ may be more
easily and positively understood by
patients, residents, and family members
than ‘‘pressure ulcer.’’ The TEP
recommended training for providers and
consumers regarding any change in
terminology. This change will be
accompanied by additional training and
guidance for providers, patients, or
residents to clarify any confusion.
Comment: One commenter suggested
that the burden of replacing the current
41 National Pressure Ulcer Advisory Panel
(NPUAP) announces a change in terminology from
pressure ulcer to pressure injury and updates the
stages of pressure injury √ The National Pressure
Ulcer Advisory Panel—NPUAP. (2016, April 13),
from https://www.npuap.org/national-pressureulcer-advisory-panel-npuap-announces-a-changein-terminology-from-pressure-ulcer-to-pressureinjury-and-updates-the-stages-of-pressure-injury/.
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measure with the modified pressure
ulcer measure will be greater than the
burden associated with reporting the
current pressure ulcer measure. The
commenter encouraged CMS to
streamline reporting and reduce
duplicative efforts. The commenter
further commented that CMS should
review the total number of data points,
including the OASIS measure set, to
eliminate HHA documentation and
administrative burden.
Response: We appreciate the
commenter’s feedback. We do not
believe that the reporting of the
proposed measure will impose a new
burden on HHAs because the measure is
calculated using data elements that are
currently included in OASIS that HHAs
already submit. As we continue to refine
and modify the OASIS, we will
continue to evaluate and avoid any
unnecessary burden associated with the
implementation of the HH QRP.
Final Decision: After consideration of
the comments received, we are
finalizing our proposal to replace the
current pressure ulcer measure, Percent
of Residents or Patients with Pressure
Ulcers That Are New or Worsened
(Short Stay) (NQF #0678), with a
modified version of that measure
entitled, Changes in Skin Integrity PostAcute Care: Pressure Ulcer/Injury,
effective with the CY 2020 HH QRP.
2. Addressing the IMPACT Act Domain
of Functional Status, Cognitive
Function, and Changes in Function and
Cognitive Function: Application of
Percent of Long-Term Care Hospital
Patients With an Admission and
Discharge Functional Assessment and a
Care Plan That Addresses Function
(NQF #2631)
a. Measure Background
Sections 1899B(c)(1)(A) of the Act
requires that no later than the specified
application date (which under section
1899B(a)(1)(E)(ii) is January 1, 2019 for
HHAs, and October 1, 2016 for SNFs,
IRFs and LTCHs), the Secretary specify
a quality measure to address the domain
of ‘‘Functional status, cognitive
function, and changes in function and
cognitive function.’’ We proposed to
adopt the measure, Application of
Percent of Long-Term Care Hospital
Patients with an Admission and
Discharge Functional Assessment and a
Care Plan That Addresses Function
(NQF #2631) for the HH QRP, beginning
with the CY 2020 program year. This is
a process measure that reports the
percentage of patients with an
admission and discharge functional
assessment and treatment goal that
addresses function. The treatment goal
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provides evidence that a care plan with
a goal has been established for the HH
patient.
The National Committee on Vital and
Health Statistics’ Subcommittee on
Health,42 noted that ‘‘information on
functional status is becoming
increasingly essential for fostering
healthy people and a healthy
population. Achieving optimal health
and well-being for Americans requires
an understanding across the life span of
the effects of people’s health conditions
on their ability to do basic activities and
participate in life situations in other
words, their functional status.’’ This is
supported by research showing that
patient and resident functioning is
associated with important outcomes
such as discharge destination and length
of stay in inpatient settings,43 as well as
the risk of nursing home placement and
hospitalization of older adults living in
the community.44 For example, many
patients who utilize HH services may be
at risk for a decline in function due to
limited mobility and ambulation.45
Thus, impairment in function activities
such as self-care and mobility is highly
prevalent in HH patients. For example,
in 98 percent of the over six million HH
episodes in 2015, the patient had at
least one limitation or was not
completely independent in self-care
activities such as grooming, upper and
lower body dressing, bathing, toilet
hygiene, and/or feeding/eating.46
The primary goal of home health care
is to provide restorative care when
improvement is expected, maintain
function and health status if
improvement is not expected, slow the
rate of functional decline to avoid
institutionalization in an acute or postacute setting, and/or facilitate transition
to end-of-life care as appropriate.47 48
42 Subcommittee on Health National Committee
on Vital and Health Statistics, ‘‘Classifying and
Reporting Functional Status’’ (2001).
43 Reistetter TA, Graham JE, Granger CV, Deutsch
A, Ottenbacher KJ. Utility of Functional Status for
Classifying Community Versus Institutional
Discharges after Inpatient Rehabilitation for Stroke.
Archives of Physical Medicine and Rehabilitation,
2010; 91:345–350.
44 Miller EA, Weissert WG. Predicting Elderly
People’s Risk for Nursing Home Placement,
Hospitalization, Functional Impairment, and
Mortality: A Synthesis. Medical Care Research and
Review, 57; 3: 259–297.
45 Kortebein, P., Ferrando, A., Lombebeida, J.,
Wolfe, R., & Evans, W.J. (2007). Effect of 10 days
of bed rest on skeletal muscle in health adults.
JAMA; 297(16):1772–4.
47 Riggs, J.S. & Madigan, E.A. (2012). Describing
variation in home health care episodes for patients
with heart failure. Home Health Care Management
and Practice, 24(3): 146–152.
48 Ellenbecker, C.H., Samia, L., Cushman, M.J., &
Alster, K (2008). Patient safety and quality: an
evidence-based handbook for nurses. Rockville
(MD): agency for healthcare research and quality
(US); 2008 Apr. Chapter 13.
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Home health care can positively impact
functional outcomes. In stroke patients,
home-based rehabilitation programs
administered by home health clinicians
significantly improved ADL function
and gait performance.49 Home health
services, delivered by a registered nurse,
positively impacted patient Quality of
Life (QOL) and clinical outcomes,
including significant improvement in
dressing lower body, bathing meal
preparation, shopping, and
housekeeping. For some home health
patients, achieving independence
within the living environment and
improved community mobility might be
the goal of care. For others, the goal of
care might be to slow the rate of
functional decline to avoid
institutionalization.50
Patients’ functional status is
associated with important patient
outcomes, so measuring and monitoring
the patients’ extent of engaging in selfcare and mobility is valuable.
Functional decline among the elderly; 51
and chronic illness comorbidities, such
as chronic pain among the older adult
population 52 53 are associated with
decreases in self-sufficiency and patient
activation (defined as the patient’s
knowledge and confidence in selfmanaging their health). Impaired
mobility, frailty, and low physical
activity are associated with
institutionalization,54 higher risk of falls
and falls-related hip fracture and
death,55 56 greater risk of under
44 Miller EA, Weissert WG. Predicting Elderly
People’s Risk for Nursing Home Placement,
Hospitalization, Functional Impairment, and
Mortality: A Synthesis. Medical Care Research and
Review, 57; 3: 259–297.
45 Kortebein, P., Ferrando, A., Lombebeida, J.,
Wolfe, R., & Evans, W.J. (2007). Effect of 10 days
of bed rest on skeletal muscle in health adults.
JAMA; 297(16):1772–4.
47 Riggs, J.S. & Madigan, E.A. (2012). Describing
variation in home health care episodes for patients
with heart failure. Home Health Care Management
and Practice, 24(3): 146–152.
48 Ellenbecker, C.H., Samia, L., Cushman, M.J., &
Alster, K (2008). Patient safety and quality: an
evidence-based handbook for nurses. Rockville
(MD): agency for healthcare research and quality
(US); 2008 Apr. Chapter 13.
49 Asiri, F.Y., Marchetti, G.F., Ellis, J.L., Otis, L.,
Sparto, P.J., Watzlaf, V., & Whitney, S.L. (2014).
Predictors of functional and gait outcomes for
persons poststroke undergoing home-based
rehabilitation. Journal of Stroke and
Cerebrovascular Diseases: The Official Journal of
National Stroke Association, 23(7), 1856–1864.
https://doi.org/10.1016/j.jstrokecerebrovasdis.2014.
02.025.
50 Ellenbecker, C.H., Samia, L., Cushman, M.J., &
Alster, K (2008). Patient safety and quality: an
evidence-based handbook for nurses. Rockville
(MD): agency for healthcare research and quality
(US); 2008 Apr. Chapter 13.
51 Gleason, K.T., Tanner, E.K., Boyd, C. M.,
Saczynski, J.S., & Szanton, S. L. (2016). Factors
associated with patient activation in an older adult
population with functional difficulties. Patient
Education and Counseling, 99(8), 1421–1426.
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nutrition,57 higher rates of inpatient
admission from the emergency
department,58 and higher prevalence of
hypertension and diabetes.59
In addition, the assessment of
functional ability and provision of
treatment plans directed toward
improving or maintaining functional
ability could impact health care costs.
Providing comprehensive home health
care, which includes improving or
maintaining functional ability for frail
elderly adults, can reduce the likelihood
of hospital readmissions or emergency
department visits, leading to reduced
health care service expenditures. 60 61 62
Reducing preventable
rehospitalizations, which made up
approximately 17 percent of Medicare’s
$102.6 billion in 2004 hospital
payments, creates the potential for large
health care cost savings.63 64
between difficulties in daily activities and falling:
loco-check as a self-assessment of fall risk.
Interactive Journal of Medical Research, 5(2), e20.
https://doi.org/10.2196/ijmr.5590.
56 Zaslavsky, O., Zelber-Sagi, S., Gray, S. L.,
LaCroix, A. Z., Brunner, R.L., Wallace, R.B., . . .
Woods, N.F. (2016). Comparison of Frailty
Phenotypes for Prediction of Mortality, Incident
Falls, and Hip Fracture in Older Women. Journal of
the American Geriatrics Society, 64(9), 1858–1862.
https://doi.org/10.1111/jgs.14233.
57 57 van der Pols-Vijlbrief, R., Wijnhoven, H.A.
H., Bosmans, J.E., Twisk, J.W.R., & Visser, M.
(2016). Targeting the underlying causes of
undernutrition. Cost-effectiveness of a
multifactorial personalized intervention in
community-dwelling older adults: A randomized
controlled trial. Clinical Nutrition (Edinburgh,
Scotland). https://doi.org/10.1016/j.clnu.2016.
09.030.
58 Hominick, K., McLeod, V., & Rockwood, K.
(2016). Characteristics of older adults admitted to
hospital versus those discharged home, in
emergency department patients referred to internal
medicine. Canadian Geriatrics Journal 202F;: CGJ,
19(1), 9–14. https://doi.org/10.5770/cgj.19.195.
59 Halaweh, H., Willen, C., Grimby-Ekman, A., &
Svantesson, U. (2015). Physical activity and healthrelated quality of life among community dwelling
elderly. J Clin Med Res, 7(11), 845–52.
60 Hirth, V., Baskins, J., & Dever-Bumba, M.
(2009). Program of all-inclusive care (PACE): Past,
present, and future. Journal of the American
Medical Directors Association, 10, 155–160.
61 Mukamel, D.B., Fortinsky, R.H., White, A.,
Harrington, C., White, L.M., & Ngo-Metzger, Q.
(2014). The policy implications of the cost structure
of home health agencies. Medicare & Medicaid
Research Review, 4(1). https://doi.org/10.5600/
mmrr2014-004-01-a03.
62 Meunier, M.J., Brant, J.M., Audet, S., Dickerson,
D., Gransbery, K., & Ciemins, E.L. (2016). Life after
PACE (Program of All-Inclusive Care for the
Elderly): A retrospective/prospective, qualitative
analysis of the impact of closing a nurse
practitioner centered PACE site. Journal of the
American Association of Nurse Practitioners.
https://doi.org/10.1002/2327-6924.12379.
63 Jencks, S.F., Williams, M.V., and Coleman, E.A.
(2009). Rehospitalizations among patients in the
Medicare fee-for-service program. New England
Journal of Medicine; 360(14):1418–28.
64 Tao, H., Ellenbecker, C.H., Chen, J., Zhan, L.,
& Dalton, J. (2012). The influence of social
environmental factors on rehospitalization among
patients receiving home health care services. ANS.
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Further, improving and maintaining
functional ability in individuals with
high needs, defined as those with three
or more chronic conditions, may also
account for an increase in healthcare
savings. Adults with three or more
chronic conditions have nearly four
times the average annual per-person
spending for health care services and
prescription medications than the
average for all U.S. adults, and high
needs adults with limitations in their
ability to perform ADLs, have even
higher average annual health care
expenditures.65 High needs individuals
with functional limitations spend, on
average, $21,021 on annual health care
services, whereas the average annual
health care expenditures for all U.S.
adults are approximately $4,845.45.
b. Measure Importance
The majority of individuals who
receive PAC services, including care
provided by HHAs, SNFs, IRFs, and
LTCHs, have functional limitations, and
many of these individuals are at risk for
further decline in function due to
limited mobility and ambulation.66 The
patient populations treated by HHAs,
SNFs, IRFs, and LTCHs vary in terms of
their functional abilities. For example,
for home health patients, achieving
independence within the home
environment and promoting community
mobility may be the goal of care. For
other home health patients, the goal of
care may be to slow the rate of
functional decline in order to allow the
person to remain at home and avoid
institutionalization.67 The clinical
practice guideline Assessment of
Physical Function 68 recommends that
clinicians document functional status at
baseline and over time to validate
capacity, decline, or progress. Therefore,
assessment of functional status at
admission and discharge, as well as
establishing a functional goal for
discharge as part of the care plan is an
Advances in Nursing Science, 35(4), 346–358.
https://doi.org/10.1097/ANS.0b013e318271d2ad.
65 Hayes, S.L., Salzberg, C.A., McCarthy, D.,
Radley, DC, Abrams, M.K., Shah, T., and Anderson,
G.F. (2016). High-Need, High-Cost Patients: Who are
they and how do they use health care—A
population-based comparison of demographics,
health care use, and expenditures. The
Commonwealth Fund.
66 Kortebein P, Ferrando A, Lombebeida J, Wolfe
R, Evans WJ. Effect of 10 days of bed rest on skeletal
muscle in health adults. JAMA; 297(16):1772–4.
67 Ellenbecker CH, Samia L, Cushman MJ, Alster
K. Patient safety and quality in home health care.
Patient Safety and Quality: An Evidence-Based
Handbook for Nurses. Vol 1.
68 Kresevic DM. Assessment of physical function.
In: Boltz M, Capezuti E, Fulmer T, Zwicker D,
editor(s). Evidence-based geriatric nursing protocols
for best practice. 4th ed. New York (NY): Springer
Publishing Company; 2012. p. 89–103.
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important aspect of patient or resident
care across PAC settings.
Currently, functional assessment data
are collected by all four PAC providers,
yet data collection has employed
different assessment instruments, scales,
and item definitions. The data cover
similar topics, but are not standardized
across PAC settings. The different sets of
functional assessment items coupled
with different rating scales makes
communication about patient and
resident functioning challenging when
patients and residents transition from
one type of setting to another. Collection
of standardized functional assessment
data across HHAs, SNFs, IRFs, and
LTCHs using common data items will
establish a common language for patient
and resident functioning, which may
facilitate communication and care
coordination as patients and residents
transition from one type of provider to
another. The collection of standardized
functional status data may also help
improve patient functioning during an
episode of care by ensuring that basic
daily activities are assessed for all PAC
residents at the start and end of care,
and that at least one functional goal is
established.
The functional assessment items
included in the proposed functional
status quality measure were originally
developed and tested as part of the PostAcute Care Payment Reform
Demonstration version of the Continuity
Assessment Record and Evaluation
(CARE) Item Set, which was designed to
standardize the assessment of a person’s
status, including functional status,
across acute and post-acute settings
(HHAs, SNFs, IRFs, and LTCHs). The
functional status items in the CARE
Item Set are daily activities that
clinicians typically assess at the time of
admission and/or discharge to
determine patient or resident needs,
evaluate patient or resident progress,
and prepare patients, residents, and
their families for a transition to home or
to another setting.
The development of the CARE Item
Set and a description and rationale for
each item is described in a report
entitled ‘‘The Development and Testing
of the Continuity Assessment Record
and Evaluation (CARE) Item Set: Final
Report on the Development of the CARE
Item Set: Volume 1 of 3.’’ 69 Reliability
and validity testing were conducted as
part of CMS’s Post-Acute Care Payment
Reform Demonstration (PAC–PRD), and
we concluded that the functional status
69 Barbara Gage et al., ‘‘The Development and
Testing of the Continuity Assessment Record and
Evaluation (CARE) Item Set: Final Report on the
Development of the CARE Item Set’’ (RTI
International, 2012).
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items have acceptable reliability and
validity. Testing for the functional
assessment items concluded that the
items were able to evaluate all patients
on basic self-care and mobility
activities, regardless of functional level
or PAC setting. A description of the
testing methodology and results are
available in several reports, including
the report entitled ‘‘The Development
and Testing of the Continuity
Assessment Record And Evaluation
(CARE) Item Set: Final Report On
Reliability Testing: Volume 2 of 3’’ 70
and the report entitled ‘‘The
Development and Testing of The
Continuity Assessment Record And
Evaluation (CARE) Item Set: Final
Report on Care Item Set and Current
Assessment Comparisons: Volume 3 of
3.’’ 71 These reports are available on our
Post-Acute Care Quality Initiatives Web
page at https://www.cms.gov/Medicare/
Quality-Initiatives-Patient-AssessmentInstruments/Post-Acute-Care-QualityInitiatives/CARE-Item-Set-and-BCARE.html.
Additional testing of these functional
assessment items was conducted in a
small field test occurring in 2016–2017,
capturing data from 12 HHAs.
Preliminary data results yielded
moderate to substantial reliability for
the self-care and mobility data items.
More information about testing design
and results can be found at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
OASIS-Data-Sets.html.
The functional status quality measure
we proposed to adopt beginning with
the CY 2020 HH QRP is a process
quality measure that is an application of
the NQF-endorsed quality measure, the
Percent of Long-Term Care Hospital
Patients with an Admission and
Discharge Functional Assessment and a
Care Plan that Addresses Function (NQF
#2631). This quality measure reports the
percent of patients with both an
admission and a discharge functional
assessment and a functional treatment
goal.
This process measure requires the
collection of admission and discharge
functional status data by clinicians
using standardized patient assessment
data elements, which assess specific
functional activities, such as self-care
and mobility activities. The self-care
and mobility function activities are
coded using a 6-level rating scale that
indicates the patient’s level of
independence with the activity at both
admission and discharge. A higher score
70 Ibid.
71 Ibid.
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indicates more independence. These
functional assessment data elements
will be collected at Start or Resumption
of Care (SOC/ROC) and discharge.
For this quality measure, there must
be documentation at the time of
admission (SOC) that at least one
activity performance (function) goal is
recorded for at least one of the
standardized self-care or mobility
function items using the 6-level rating
scale. This indicates that an activity
goal(s) has been established. Following
this initial assessment, the clinical best
practice will be to ensure that the
patient’s care plan reflected and
included a plan to achieve such activity
goal(s). At the time of discharge, goal
setting and establishment of a care plan
to achieve the goal, is reassessed using
the same 6-level rating scale, allowing
for the ability to evaluate success in
achieving the patient’s activity
performance goals.
To the extent that a patient has an
unplanned discharge, for example,
transfer to an acute care facility, the
collection of discharge functional status
data may not be feasible. Therefore, for
patients with unplanned discharges,
admission functional status data and at
least one treatment goal must be
reported, but discharge functional status
data are not required to be reported.
c. Stakeholder Feedback
Our measures contractor convened a
TEP on October 17 and October 18,
2016. The TEP was composed of a
diverse group of stakeholders with HH,
PAC, and functional assessment
expertise. The panel provided input on
the technical specifications of this
proposed measure, including the
feasibility of implementing the measure,
as well as the overall measure of
reliability and validity. The TEP
additionally provided feedback on the
clinical assessment items used to
calculate the measure. The TEP
reviewed the measure ‘‘Percent of LongTerm Care Patients with an Admission
and Discharge Functional Assessment
and a Care Plan That Addresses
Function (NQF 2631)’’ for potential
application to the home health setting.
Overall they were supportive of a
functional process measure, noting it
could have the positive effect of
focusing clinician attention on
functional status and goals. A summary
of the TEP proceedings is available on
the PAC Quality Initiatives Downloads
and Videos Web page at https://
www.cms.gov/medicare/qualityinitiatives-patient-assessmentinstruments/post-acute-care-qualityinitiatives/impact-act-of-2014/impactact-downloads-and-videos.html.
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We also solicited stakeholder
feedback on the development of this
measure through a public comment
period held from November 4, 2016
through December 5, 2016. Several
stakeholders and organizations
supported this measure for
implementation and for measure
standardization. Some commenters also
provided feedback on the standardized
patient assessment data elements used
to calculate the proposed quality
measure. Commenters offered
suggestions, including providing
education regarding the difference in
measure scales for the standardized
items relative to current OASIS
functional items, and guidance on the
type of clinical staff input needed to
appropriately complete new functional
assessment items. Commenters also
addressed the feasibility of collecting
data for the individual standardized
self-care and mobility items in the home
health setting. Finally, commenters
noted the importance of appropriate
goal setting when functional
improvement for a patient may not be
feasible. The public comment summary
report for the proposed measure is
available on the CMS Web site at
https://www.cms.gov/medicare/qualityinitiatives-patient-assessmentinstruments/post-acute-care-qualityinitiatives/impact-act-of-2014/impactact-downloads-and-videos.html.
The NQF-convened MAP met on
December 14 and 15, 2016, and
provided input on the use of this
proposed measure in the HH QRP. The
MAP recommended ‘‘conditional
support for rulemaking’’ for this
measure. MAP members noted the
measure will drive care coordination
and improve transitions by encouraging
the use of standardized functional
assessment items across PAC settings,
but recommended submission to the
NQF for endorsement to include the
home health setting. More information
about the MAP’s recommendations for
this measure is available at https://
www.qualityforum.org/Publications/
2017/02/MAP_2017_Considerations_
for_Implementing_Measures_in_
Federal_Programs_-_PAC-LTC.aspx.
We reviewed the NQF’s consensus
endorsed measures and were unable to
identify any home health measures that
address functional assessment and
treatment goals that that address
function. However, we were able to
identify five functional measures in
home health that assess functional
activities only, without a treatment goal.
These measures are: (1) Improvement in
Ambulation/Locomotion (NQF #0167);
(2) Improvement in Bathing (NQF
#0174); (3) Improvement in Bed
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Transfer (NQF #0175); (4) Improvement
in Management of Oral Medications
(NQF # 0176); and (5) Improvement in
Pain Interfering with Activity (NQF
#0177). Our review determined that
these setting-specific measures are not
appropriate to meet the specified
IMPACT Act domain as they do not
include standardized items or are not
included for various other PAC
populations. Specifically—
• The items used to collect data for
the current home health measures are
less specific, leading to broader measure
results, whereas the standardized
patient assessment data items used for
the proposed measure assess core
activities such as rolling in bed, walking
a specified distance, or wheelchair
capability.
• The item coding responses are more
detailed when compared to the nonstandardized OASIS item responses,
allowing for more granular data for the
measure.
• The proposed functional measure
will capture a patient’s discharge goal at
admission into home health; this detail
is not captured in the existing endorsed
HH function measures.
Therefore, based on the evidence
discussed previously, we proposed to
adopt the quality measure entitled,
Application of Percent of Long-Term
Care Hospital Patients with an
Admission and Discharge Functional
Assessment and a Care Plan That
Addresses Function (NQF #2631), for
the HH QRP beginning with the CY
2020 HH QRP. We noted that we plan
to submit the proposed measure to the
NQF for endorsement consideration as
soon as is feasible.
For technical information about the
proposed measure, including
information about the measure
calculation and the standardized patient
assessment data elements used to
calculate this measure, we referred
readers to the document titled, Final
Specifications for HH QRP Quality
Measures and Standardized Patient
Assessment Data, available at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HHQIQualityMeasures.html.
d. Data Collection
For purposes of assessment data
collection, we proposed to add new
functional status items to the OASIS, to
be collected at SOC/ROC and discharge.
These items will assess specific self-care
and mobility activities, and will be
based on functional items included in
the PAC–PRD version of the CARE Item
Set. More information pertaining to item
testing is available on our Post-Acute
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Care Quality Initiatives Web page at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Post-Acute-Care-QualityInitiatives/CARE-Item-Set-and-BCARE.html.
To allow HHAs to fulfill the
requirements of the Home Health
Agency Conditions of Participation
(HHA CoPs) (82 FR 4509), we proposed
to add a subset of the functional
assessment items to the OASIS, with
collection of these items at Follow-Up
(FU). The collection of these assessment
items at FU by HHAs will allow them
to fulfill the requirements outlined in
the HHA CoPs that suggest that the
collection of a patient’s current health,
including functional status, be collected
on the comprehensive assessment.
This new subset of functional status
items are standardized across PAC
settings and support the proposed
standardized measure. They are
organized into two functional domains:
Self-Care and Mobility. Each domain
includes dimensions of these functional
constructs that are relevant for home
health patients. The proposed function
items that we proposed to add to the
OASIS for purposes of the calculation of
this proposed quality measure would
not duplicate existing items currently
collected in that assessment instrument
for other purposes. The current OASIS
function items evaluate current ability,
whereas the proposed functional items
would evaluate an individual’s usual
performance at the time of admission
and at the time of discharge for goal
setting purposes. Additionally, we
noted that there are several key
differences between the existing and
new proposed function items that may
result in variation in the patient
assessment results including: (1) The
data collection and associated data
collection instructions; (2) the rating
scales used to score a resident’s level of
independence; and (3) the item
definitions. A description of these
differences is provided with the
measure specifications available at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HHQIQualityMeasures.html.
Because of the differences between
the current function assessment items
(OASIS C–2) and the proposed function
assessment items that we would collect
for purposes of calculating the proposed
measure, we would require that HHAs
submit data on both sets of items. Data
collection for the new proposed
function items do not substitute for the
data collection under the current OASIS
ADL and IADL items, and as discussed
previously, we do not believe that the
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items are duplicative. However, we
solicited comment on opportunities to
streamline reporting to avoid
duplication and minimize burden.
We proposed that data for the
proposed quality measure would be
collected through the OASIS, which
HHAs currently submit through the
QIES ASAP system. We referred readers
to section V.F.2 of the proposed rule (82
FR 35345 through 35353) for more
information on the proposed data
collection and submission timeline for
this proposed quality measure. We
noted that if this measure is finalized,
we intended to provide initial
confidential feedback to home health
agencies, prior to the public reporting of
this measure.
We solicited public comment on our
proposal to adopt the measure,
Application of Percent of Long-Term
Care Hospital Patients with an
Admission and Discharge Functional
Assessment and a Care Plan That
Addresses Function (NQF #2631).
Comment: A number of commenters
supported the proposed measure,
Application of Percent of Long-Term
Care Hospital Patients with an
Admission and Discharge Functional
Assessment and a Care Plan That
Addresses Function (NQF #2631).
MedPAC acknowledged the value of a
functional status quality measure that
would be standardized with other
functional status quality measures
across the four PAC settings.
Response: We appreciate the
commenters’ support of the measure.
Comment: Some commenters
suggested that CMS refine the measure
and conduct additional testing for home
health setting applicability before
adopting it Other commenters
recommended that we provide training
and give HHAs time to adjust their
workflow to both accommodate the new
measure and the removal of duplicative
data elements in the OASIS. Further, a
few commenters expressed concern over
the addition of the items used to
calculate the proposed process quality
measure, claiming that the items will be
duplicative and that the legacy items
must be removed from the OASIS–C2
assessment instrument to limit provider
burden. Commenters also requested that
CMS consider the additional resources
providers will need to accommodate
item set changes and encouraged
ongoing education efforts for new data
elements.
Response: The items for this measure
were rigorously tested in the Post-Acute
Care Payment Reform Demonstration
(PAC PRD). Based on testing from the
PAC PRD, the inter-rater reliability of
the items needed to calculate this
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measure was favorable, with items’
kappa scores between 0.59 and 0.80.
This is important for measuring progress
in some of the most complex cases
treated in post-acute care settings. The
data elements developed to calculate
this proposed process measure were
also tested in a comprehensive field test
of existing and potential OASIS data
elements and found to be feasible with
acceptable levels of inter-rater
reliability, as described at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
OASIS-Data-Sets.html.
Although HHAs will need to
incorporate the data on this measure
into their workflow, we do not believe
that these data elements are duplicative
of other data already collected. The
items needed to calculate the proposed
measure different assessment scales,
coding options for those with medical
complexities, and have different
definitions for items and activities, and
the proposed measure’s data elements
evaluate usual performance in various
manners. Further, to reduce potential
burden associated with collecting the
proposed measure, we have included
several mechanisms to reduce the
number of items that apply to any one
patient. For example, there are gateway
questions pertaining to walking and
wheelchair mobility that allow the
clinician to skip items that ask if the
patient does not walk or does not use a
wheelchair, respectively.
Comment: Commenters provided
feedback on the reliability and validity
of the items necessary to calculate the
function process measure. Some of these
commenters expressed concern that the
proposed function measure has not
undergone testing and validation in the
home health setting or may not be
applicable for home health setting as in
the facility-based post-acute care
settings. One of these commenter
expressed concern that the scales used
to assess the items for the proposed
process quality measure and the current
OASIS functional assessment items are
different, which could affect the items’
reliability and validity. Another
commenter raised concern with the
difference in timeframe allowed for data
collection when compared to other
OASIS items.
Response: In the PAC PRD, the
functional activity items (self-care and
mobility) were tested sufficiently in
HHAs and with sufficient patients to
support reliability. The functional
assessment items were compared to
other functional assessment instrument
data (including OASIS functional
assessment items), as part of the PAC–
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PRD analyses with positive results. The
inter-rater reliability of the functional
activity items has been tested and the
results have been favorable with items’
kappa scores between .59 and .80. We
also conducted analyses of the internal
consistency of the function data
analyses which indicate moderate to
substantial agreement suggesting
sufficient reliability for the items used
to calculate the proposed process
quality measure.
We acknowledge that the scale for the
items used to calculate the proposed
quality measure vary from the scales
that are used in current OASIS–C2
items. The scale used to assess the items
for the proposed process quality
measure assesses independence in
functional activities (a higher score
indicates greater independence). We
believe that the 6-level scale will allow
us to better distinguish change at the
highest and lowest levels of patient
functioning by documenting minimal
change from no change at the low end
of the scale.72 The PAC PRD supported
the use of the scale in HHAs with both
the alpha testing and beta testing
reinforcing the clinical logic and
consistency of language for the
functional assessment items. The items
in section GG were developed with
input from clinicians and stakeholders
to better measure the change in
function, regardless of the severity of
the individual’s impairment.
The items used to calculate the
proposed process quality measure are
standardized across the four PAC
settings, based on the need for data to
reflect the patient’s status at the time of
SOC/ROC and EOC. We are currently
conducting testing across the four PAC
settings to align the most appropriate
time frame of data collection at
admission/SOC and at discharge/EOC.
A full description of the analyses and
the results are provided in the report,
The Development and Testing of the
Continuity Assessment Record and
Evaluation (CARE) Item Set: Final
Report on the Development of the CARE
Item Set and Current Assessment
Comparisons Volume 3 of 3, and the
report is available at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Post-Acute-Care-QualityInitiatives/CARE-Item-Set-and-BCARE.html. Additional testing of the
Section GG items with the OASIS
functional items was recently completed
72 Barbara Gage et al., ‘‘The Development and
Testing of the Continuity Assessment Record and
Evaluation (CARE) Item Set: Final Report on the
Development of the CARE Item Set’’ (RTI
International, 2012).
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and will to continue to help inform
guidance for HH providers.
Comment: One commenter suggested
that the OASIS should include an
assessment of Instrumental Activities of
Daily Living (IADL) as a part of
functional assessment.
Response: We appreciate the
commenter’s recommendation and will
take it into consideration in future
measure refinement work.
Comment: Commenters expressed
concern about different clinical staff
assessing functional status and setting
functional goals across PAC settings,
noting that in some settings, such as
SNFs, licensed physical therapists
typically assess function and set
functional goals, whereas in HHAs,
nurses typically perform that
assessment. Commenters noted that
setting a goal will pose a challenge for
nurses in the home health setting.
Response: We are unclear why the
commenters believe that goal setting
will be more difficult in the home
health setting than in other settings. The
goals being assessed through the
measure are intended to be set by
patients, not clinicians. In addition, the
original testing of the assessment items
used for the proposed measure included
a wide variety of clinicians to assess
item collection, coding and reliability.
For more information on testing results,
we refer readers to the PAC PRD final
report located at: https://www.cms.gov/
Medicare/Quality-Initiatives-PatientAssessment-Instruments/Post-AcuteCare-Quality-Initiatives/Downloads/
The-Development-and-Testing-of-theContinuity-Assessment-Record-andEvaluation-CARE-Item-Set-Final-Reporton-the-Development-of-the-CARE-ItemSet-Volume-1-of-3.pdf.
Final Decision: After consideration of
the comments received, we are
finalizing, as proposed, the adoption of
the measure entitled the Application of
Percent of Long-Term Care Hospital
Patients with an Admission and
Discharge Functional Assessment and a
Care Plan That Addresses Function
(NQF #2631) for the HH QRP beginning
with the CY 2020 program year.
asabaliauskas on DSKBBXCHB2PROD with RULES
3. Addressing the IMPACT Act Domain
of ‘‘Incidence of Major Falls’’ Measure:
Percent of Residents Experiencing One
or More Falls With Major Injury
a. Measure Background
Section 1899B(c)(1)(D) of the Act
requires that no later than the specified
application date (which under section
1899B(a)(1)(E)(i)(IV) of the Act is
January 1, 2019 for HHAs, and October
1, 2016 for SNFs, IRFs and LTCHs), the
Secretary specify a measure to address
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the domain of incidence of major falls,
including falls with major injury. We
proposed to adopt the measure,
Application of Percent of Residents
Experiencing One or More Falls with
Major Injury (NQF #0674), for which we
would begin to collect data on January
1, 2019 for the CY 2020 HH QRP to meet
this requirement. This proposed
outcome measure reports the percentage
of patients who have experienced falls
with major injury during episodes
ending in a 3-month period.
b. Measure Importance
Falls affect an estimated 6 to 12
million older adults each year and are
the leading cause of both fatal injury
and nonfatal hospital admissions.73 74
Within the home health population, the
risk of falling is significant as
approximately one third of individuals
over the age of 65 experienced at least
one fall annually.75 Major fall-related
injuries among older communitydwelling adults are a growing health
concern within the United States 76 77
because they can have high medical and
cost implications for the Medicare
community.78 In 2013, the direct
medical cost for falls in older adults was
$34 billion 79 and is projected to
increase to over $101 billion by 2030
due to the aging population.80
Evidence from various studies
indicates that implementing effective
fall prevention interventions and
73 Bohl, A.A., Phelan, E.A., Fishman, P.A., &
Harris, J R. (2012). How are the costs of care for
medical falls distributed? The costs of medical falls
by component of cost, timing, and injury severity.
The Gerontologist, 52(5): 664–675.
74 National Council on Aging (2015). Falls
Prevention Fact Sheet. Retrieved from https://
www.ncoa.org/wp-content/;uploads/FactSheet_Falls-Prevention.pdf.
75 Avin G.K., Hanke A.T., Kirk-Sanche, N.,
McDonough M.C., Shubert E.T., Hardage, J.,&
Hartley, G. (2015). Management of Falls in
Community-Dwelling Older Adults: Clinical
Guidance Statement From the Academy of Geriatric
Physical Therapy of the American Physical Therapy
Association. Physical Therapy, 95(6), 815–834.
doi:10.2522/ptj.20140415.
76 Hester, A.L. & Wei, F. (2013). Falls in the
community: State of the science. Clinical
Interventions in Aging, 8:675–679.
77 Orces, C.H. & Alamgir, H. (2014). Trends in fallrelated injuries among older adults treated in
emergency departments in the USA. Injury
Prevention, 20: 421–423.
78 Liu, S.W., Obermeyer, Z., Chang, Y., & Shankar,
K.N. (2015). Frequency of ED revisits and death
among older adults after a fall. American Journal of
Emergency Medicine, 33(8), 1012–1018.
doi:10.1016/j.ajem.2015.04.023.
79 Centers for Disease Control and Prevention
(2015b). Important facts about falls. https://
www.cdc.gov/homeandrecreationalsafety/falls/
adultfalls.html. Accessed April 19, 2016.
80 Houry, D., Florence, C. Bladwin, G., Stevens, J.,
& McClure, R. (2015). The CDC Injury Center’s
response to the growing public health problem of
falls among older adults. American Journal of
Lifestyle Medicine, 10(1), 74–77.
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minimizing the impact of falls that do
occur reduces overall costs, emergency
department visits, hospital
readmissions, and overall Medicare
resource utilization.81 82 83 84 In the 2006
Home Assessments and Modification
study, a home visit by an occupational
therapist or home care worker to
identify and mitigate potential home
hazards and risky behavior, resulted in
a 46 percent reduction in fall rates for
those receiving the intervention
compared to controls.85 Overall,
patients participating in interventions
experienced improved quality of life
due to reduced morbidity, improved
functional ability and mobility, reduced
number of falls and injurious falls, and
a decrease in the fear of falling.86 87
Falls also represent a significant cost
burden to Medicare. Each year, 2.8
million older people are treated in
Emergency Departments for fall related
injuries and over 800,000 require
hospitalization.88 Adjusted to 2015
dollars, nationally, direct medical costs
for nonfatal fall related injuries in older
adults were over $31.3 billion.89
Additional health care costs (in 2010
dollars) can range from $3,500 for a fall
without serious injury to $27,000 for a
81 Bamgbade, S., & Dearmon, V. (2016). Fall
prevention for older adults receiving home
healthcare. Home Healthcare Now, 34(2), 68–75.
82 Carande-Kulis, V., Stevens, J.A., Florence, C.S.,
Beattie, B.L., & Arias, I. (2015). A cost–benefit
analysis of three older adult fall prevention
interventions. Journal of Safety Research, 52, 65–70.
doi:10.1016/j.jsr.2014.12.007.
83 Cohen, A.M., Miller, J., Shi, X., Sandhu, J., &
Lipsitz, A. (2015). Prevention program lowered the
risk of falls and decreased claims for long-term care
services among elder participants. Health Affairs,
34(6), 971–977.
84 Howland, J., Shankar, K.N., Peterson, E.W., &
Taylor, A.A. (2015). Savings in acute care costs if
all older adults treated for fall-related injuries
completed matter of balance. Injury Epidemiology,
2(25), 1–7.
85 Pighills AC, Torgerson DJ, Sheldon TA,
Drummond AE, Bland JM. Environmental
assessment and modification to prevent falls in
older people. Journal of the American Geriatrics
Society. 2011;59(1):26–33.
86 Chase, C.A., Mann, K., Wasek, S., & Arbesman,
M. (2012). Systematic review of the effect of home
modification and fall prevention programs on falls
and the performance of community-dwelling older
adults. American Journal of Occupational Therapy,
66(3), 284–291.
87 Patil, R., Uusi-Rasi, K., Tokola, K., Karinkanta,
S., Kannus, P., & Sievanen, H. (2015). Effects of a
Multimodal Exercise Program on Physical Function,
Falls, and Injuries in Older Women: A 2-Year
Community-Based, Randomized Controlled Trial.
Journal of the American Geriatrics Society, 63(7),
1306–1313.
88 Centers for Disease Control and Prevention,
National Center for Injury Prevention and Control.
Web–based Injury Statistics Query and Reporting
System (WISQARS) [online]. Accessed August 5,
2016.
89 Burns ER, Stevens JA, Lee R. The direct costs
of fatal and non-fatal falls among older adults—
United States. J Safety Res 2016;58:99–103.
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fall with a serious injury.90 Between
1988 and 2005, fractures accounted for
84 percent of hospitalizations for fallrelated injuries among older adults.91
Researchers evaluated the cost of fallrelated hospitalizations among older
adults using the 2011 Texas Hospital
Inpatient Discharge Data and
determined that the average cost for fallrelated hip fractures was $61,715 for
individuals 50 and older living in
metropolitan areas and $55,366 for
those living nonmetropolitan areas.92
To meet the IMPACT Act provision
requiring the development of a
standardized quality measure for the
domain of Incidence of Major Falls
(sections 1899B(c)(1)(D) of the Act), we
proposed the standardized measure, The
Percent of Residents Experiencing One
or More Falls with Major Injury (Long
Stay) (NQF #0674). We noted that this
quality measure is NQF-endorsed and
has been successfully implemented in
the Nursing Home Quality Initiative for
nursing facility long-stay residents since
2011, demonstrating the measure is
feasible, appropriate for assessing PAC
quality of care, and could be used as a
platform for standardized quality
measure development. This quality
measure is standardized across PAC
settings and contains items that are
collected uniformly in each setting’s
assessment instruments (that is, MDS,
IRF–PAI, and LCDS). Further, an
application of the quality measure was
adopted for use in the LTCH QRP in the
FY 2014 IPPS/LTCH PPS final rule (78
FR 50874 through 50877), revised in the
FY 2015 IPPS/LTCH PPS final rule (79
FR 50290 through 50291), and adopted
to fulfill IMPACT Act requirements in
the FY 2016 IPPS/LTCH PPS final rule
(80 FR 49736 through 49739). Data
collection began in April 1, 2016 for
LTCHs, and October 1, 2016 for SNFs
and IRFs.
More information on the NQFendorsed quality measure, the Percent
of Residents Experiencing One or More
Falls with Major Injury (Long Stay)
(NQF #0674) is available at https://
www.qualityforum.org/QPS/0674.
90 Wu S, Keeler EB, Rubenstein LZ, Maglione MA,
Shekelle PG. A cost-effectiveness analysis of a
proposed national falls prevention program. Clin
Geriatr Med. 2010;26(4): 751–66.
91 Orces, C.H. & Alamgir, H. (2014). Trends in fallrelated injuries among older adults treated in
emergency departments in the USA. Injury
Prevention, 20: 421–423.
92 Towne, S.D., Ory, M.G., & Smith, M.L. (2014).
Cost of fall-related hospitalizations among older
adults: Environmental comparisons from the 2011
Texas hospital inpatient discharge data. Population
Health Management, 17(6), 351–356.
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c. Stakeholder Feedback
A TEP convened by our measure
development contractor provided input
on the technical specifications of an
application of the quality measure, the
Percent of Residents Experiencing One
or More Falls with Major Injury (Long
Stay) (NQF #0674), including the
feasibility of implementing the measure
across PAC settings. The TEP was
supportive of the implementation of this
measure across PAC settings and was
also supportive of our efforts to
standardize this measure for crosssetting development. More information
about this TEP can be found at https://
www.cms.gov/medicare/qualityinitiatives-patient-assessmentinstruments/post-acute-care-qualityinitiatives/impact-act-of-2014/impactact-downloads-and-videos.html.
In addition, we solicited public
comment on this measure from
September 19, 2016, through October
14, 2016. Overall, commenters were
generally supportive of the measure, but
raised concerns about the attribution
given that home health clinicians are
not present in the home at all times and
recommended risk-adjusting the
measure. The summary of this public
comment period can be found at https://
www.cms.gov/medicare/qualityinitiatives-patient-assessmentinstruments/post-acute-care-qualityinitiatives/impact-act-of-2014/impactact-downloads-and-videos.html.
Finally, we presented this measure to
the NQF-convened MAP on December
14, 2016. The MAP conditionally
supported the use of an application of
the quality measure, the Percent of
Residents Experiencing One or More
Falls with Major Injury (Long Stay)
(NQF #0674) in the HH QRP as a crosssetting quality measure. The MAP
highlighted the clinical significance of
falls with major injury, while noting
potential difficulties in collecting falls
data and more limited action ability in
the home health setting. The MAP
suggested that CMS explore
stratification of measure rates by referral
origin when public reporting. More
information about the MAP’s
recommendations for this measure is
available at https://
www.qualityforum.org/Publications/
2017/02/MAP_2017_Considerations_
for_Implementing_Measures_in_
Federal_Programs_-_PAC-LTC.aspx. We
solicited public comment on the
stratification of the proposed measure,
specifically on the measure rates for
public reporting. The quality measure,
the Percent of Residents Experiencing
One or More Falls with Major Injury
(Long Stay) (NQF #0674) is not
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currently endorsed for the home health
setting. We reviewed the NQF’s
consensus endorsed measures and were
unable to identify any NQF-endorsed
cross-setting quality measures for that
setting that are focused on falls with
major injury. We found one falls-related
measure in home health titled,
Multifactor Fall Risk Assessment
Conducted for All Patients Who Can
Ambulate (NQF #0537).
We noted that we are also aware of
one NQF-endorsed measure, Falls with
Injury (NQF #0202), which is a measure
designed for adult acute inpatient and
rehabilitation patients capturing ‘‘all
documented patient falls with an injury
level of minor or greater on eligible unit
types in a calendar quarter, reported as
injury falls per 100 days.’’ 93 After
careful review, we determined that
these measures are not appropriate to
meet the IMPACT Act domain of
incidence of major falls. Specifically—
• NQF #0202 includes minor injuries
in the numerator definition. Including
all falls in an outcome measure could
result in providers limiting activity for
individuals at higher risk for falls.
• NQF #0537 is a process-based
measure of HHAs’ efforts to assess the
risk for any fall, but not actual falls.
• Neither measure is standardized
across PAC settings.
We are unaware of any other crosssetting quality measures for falls with
major injury that have been endorsed or
adopted by another consensus
organization for the Home health
setting. Therefore, based on the
evidence discussed previously, we
proposed to adopt the quality measure
entitled, An Application of the Measure
Percent of Residents Experiencing One
or More Falls with Major Injury (Long
Stay) (NQF #0674), for the HH QRP
beginning with the CY 2020 HH QRP.
We noted in the proposed rule that we
plan to submit the proposed measure to
the NQF for endorsement consideration
as soon as it is feasible.
d. Data Collection
For purposes of assessment data
collection, we proposed to add two new
falls-related items to the OASIS. The
proposed falls with major injury item
used to calculate the proposed quality
measure does not duplicate existing
items currently collected in the OASIS.
We proposed to add two standardized
items to the OASIS for collection at
EOC, which comprises the Discharge
from Agency, Death at Home, and
Transfer to an Inpatient Facility time
93 American Nurses Association (2014, April 9).
Falls with injury. Retrieved from https://
www.qualityforum.org/QPS/0202.
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points: J1800 and J1900. The first item
(J1800) is a gateway item that asks
whether the patient has experienced any
falls since admission/resumption of care
(prior assessment). If the answer to
J1800 is yes, the next item (J1900) asks
for the number of falls with: (a) No
injury, (b) injury (except major), and (c)
major injury. The measure is calculated
using data reported for J1900C (number
of falls with major injury). This measure
would be calculated at the time of
discharge (see 82 FR 35351). For
technical information about this
proposed measure, including
information pertaining to measure
calculation and the standardized patient
assessment data element used to
calculate this measure, we referred
readers to the document titled, Final
Specifications for HH QRP Quality
Measures and Standardized Patient
Assessment Data, available at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HHQIQualityMeasures.html.
We proposed that data for the
proposed quality measure would be
collected through the OASIS, which
HHAs currently submit through the
QIES ASAP system. We referred readers
to section V.I.4 of the proposed rule for
more information on the proposed data
collection and submission timeline for
this proposed quality measure.
We solicited public comments on our
proposal to adopt an application of the
quality measure, the Percent of
Residents Experiencing One or More
Falls with Major Injury (Long Stay)
(NQF #0674) beginning with the CY
2020 HH QRP.
Comment: A few commenters
supported the proposed measure,
Application of Percent of Residents
Experiencing One or More Falls With
Major Injury (Long Stay) (NQF #0674),
noting that it aligned with measures in
other post-acute care settings.
Response: We appreciate the
commenters’ support of the proposed
measures.
Comment: Several commenters
suggested that CMS further refine and
test Application of Percent of Residents
Experiencing One or More Falls With
Major Injury (Long Stay) (NQF #0674),
to determine HHA setting applicability
before adopting it for the HH QRP.
Other commenters recommended that
we provide training and time for HHAs
to accommodate the new measures into
their workflow. One commenter
recommended that we review the
impact of new measures on high needs
beneficiaries.
Response: This measure is fully
developed and testing of this measure is
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based on a comprehensive field test of
the items used to calculate this measure.
Further, feedback from clinicians
suggested that the items used to
calculate this measure are feasible to
collect in a Home health setting,
reinforcing the measure testing by CMS
and their measure contractor. Therefore,
by way of testing results and consensus
vetting, we believe that this measure is
applicable to a home health setting.
With respect to training, we intend to
engage in multiple activities including
updating our manual and conducting
training sessions, to ensure that HHAs
understand how to properly report the
measure.
Comment: A few commenters
addressed the administrative burden of
the measure, specifically focusing on
the addition of items used in its
calculation to the OASIS. Specifically,
one of these commenters encouraged
CMS to review the overall number of
OASIS data elements and measures. The
same commenter noted that HHAs
already are evaluated on a falls measure,
‘‘Multifactor Fall Risk Assessment
Conducted for All Patients Who Can
Ambulate’’.
Response: This proposed measure is
an outcome measure that we are
adopting to satisfy the measure domain,
Incidence of Major Falls, required by the
IMPACT Act. The process measure,
‘‘Multifactor Fall Risk Assessment
Conducted for All Patients Who Can
Ambulate’’, is a measure that assesses
falls risk rather than the outcome of a
major fall. That measure is not aligned
across post-acute care settings and
therefore does not meet the
requirements of the IMPACT Act.
Pertaining to the administrative
burden, the proposed measure, ‘‘Falls
with Major Injury,’’ requires a total of
two items to be added to the OASIS,
which were considered feasible for
collection in post-acute care settings.
We believe these items add minimally
to the quality reporting burden.
Comment: Several commenters noted
that the home health setting is unique
from facility-based care, making it
difficult to assess or prevent patient
falls. Commenters noted that home
health staff are not with their patients
around the clock, unlike facility-based
care, and that patients may refuse or
decline to follow staff recommendations
on falls prevention.
Response: Assessing the incidence of
major falls, which is associated with
morbidity, mortality, and high costs, is
required under the IMPACT Act and is
also one of our major priorities for
improving the quality of patient care. In
order to ensure that this measure is
appropriate for a home health setting,
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51729
we examined fall risk and prevalence
among the cohort of home health
patients by means of an analysis using
2015 OASIS data. In nearly 32 percent
of the 5.3 million episodes with relevant
data, the patient had a history of falls,
defined as two or more falls, or any fall
with an injury, in the previous 12
months. For the more than 6.1 million
episodes where the patient received a
multi-factor falls risk assessment using
a standardized, validated assessment
tool, the patient was found to have falls
risk 93 percent of the time.
Additionally, there were nearly 100,000
instances documented where a patient
required emergency care for an injury
due to a fall. Our environmental scan
identified evidence-based strategies that
can and have been applied in the home
health setting to reduce falls risk.
Therefore, we believe that a measure of
this type is important for both providers
and individuals, to support personcentered care to properly assess for the
risk of falling accompanied by a major
injury to support proper care planning.
In addition to meeting the requirements
of the IMPACT Act, this measure will
address the current gap in the HH QRP
measure set for this type of injurious
fall.
Comment: Several commenters
recommended that this measure be riskadjusted for the purpose of publicreporting, and that unadjusted rates be
shared with providers via confidential
feedback only. Commenters additionally
suggested that there may be unintended
consequences without risk adjustment
such that HHAs may be hesitant to
accept higher falls’ risk patients for fear
of the financial impact. The commenters
stated that this may potentially limit the
value of comparison amongst HHAs.
According to one of these commenters,
without risk adjustment, the measure
could present a distorted correlation
between the rate of major injuries
related to falls and the quality of care
provided by the agency. This will limit
comparisons among home health
agencies. Another commenter noted that
stratifying results for public reporting
may not be feasible given sample sizes
and will not be a substitute for riskadjustment.
Response: While we acknowledge that
various patient characteristics can
elevate the risk for falls, falls with major
injury are considered to be ‘never
events. A never event is a serious
reportable event. For that reason, we do
not believe we should risk adjust the
proposed measure. Risk adjusting for
falls with major injury could
unintentionally lead to insufficient risk
prevention by the provider. The need
for risk assessment, based on varying
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risk factors among residents, does not
remove the obligation of providers to
minimize that risk.
Comment: Many commenters noted
that the falls measure is not endorsed by
NQF for the home health setting and
encouraged CMS to pursue NQF
endorsement.
Response: While this measure is not
currently NQF-endorsed, we recognize
that the NQF endorsement process is an
important part of measure development
and we plan to submit this measure for
NQF endorsement consideration as soon
as feasible.
Final Decision: After consideration of
the comments received, we are
finalizing as proposed the measure
Percent of Residents Experiencing One
or More Falls with Major Injury for
adoption in the HH QRP beginning with
the CY 2020 program year.
G. HH QRP Quality Measures and
Measure Concepts Under Consideration
for Future Years
We solicited public comment on the
importance, relevance, appropriateness,
and applicability of each of the quality
measures listed in Table 19 for use in
future years in the HH QRP.
TABLE 19—HH QRP QUALITY MEASURES UNDER CONSIDERATION FOR FUTURE YEARS
IMPACT Act domain
Functional status, cognitive function, and changes in function and cognitive function
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Measures ............................................................
We noted that we are considering four
measures that will assess a change in
functional outcomes such as self-care
and mobility across a HH episode.
These measures would be standardized
to measures finalized in other PAC
quality reporting programs, such as the
IRF QRP. We solicited feedback on the
importance, relevance, appropriateness,
and applicability of these measure
constructs.
Based on input from stakeholders, we
have identified additional concept areas
for potential future measure
development for the HH QRP. These
include claims-based within stay
potentially preventable hospitalization
measures. The potentially preventable
within-stay hospitalization measures
will look at the percentage of HH
episodes in which patients were
admitted to an acute care hospital or
seen in an emergency department for a
potentially preventable condition
during an HH episode. We solicited
feedback on the importance, relevance,
appropriateness, and applicability of
these measure constructs.
In alignment with the requirements of
the IMPACT Act to develop quality
measures and standardize data for
comparative purposes, we believe that
evaluating outcomes across the postacute settings using standardized data is
an important priority. Therefore, in
addition to proposing a process-based
measure for the domain of ‘‘Functional
status, cognitive function, and changes
in function and cognitive function’’,
included in the proposed rule, we noted
that we also intended to develop
outcomes-based quality measures,
including functional status and other
quality outcome measures to further
satisfy this domain.
Comment: Three commenters
expressed general support for the
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A. Application of NQF #2633—Change in Self-Care Score for Medical Rehabilitation Patients.
B. Application of NQF #2634—Change in Mobility Score for Medical Rehabilitation Patients.
C. Application of NQF #2635—Discharge Self-Care Score for Medical Rehabilitation Patients.
D. Application of NQF #2636—Discharge Mobility Score for Medical Rehabilitation Patients.
measures under consideration for future
years. These commenters stated that
measures should be tested in the home
health setting prior to being finalized,
highlighting that the home setting is
different than other standardized
institutional care settings and presents
unique challenges to caregivers and
beneficiaries. One of the commenters
stated that the measurement domains
are critically important in the home
health setting and highly relevant,
especially for patients whose goal is
improvement, adding that the relevance,
appropriateness, and applicability can
only be discussed after validity and
reliability testing is completed in the
home health setting. Another
commenter suggested leveraging
changes in quality measures as an effort
to safeguard the delivery of therapy
services and ensure accountability on
the part of the provider.
Response: We appreciate the
recommendations and comments. We
agree that all future measures should be
adequately tested and found reliable for
the home health setting.
Comment: Commenters supported the
development of functional status
measures. MedPAC also supported
measures that cut-across sectors, as long
as they are standardized, and noted they
would support the self-care and
mobility measure concepts for HHAs
based on the IRF measure specifications,
as long as CMS ensured that the
measures are aligned across PAC
settings. A few commenters
recommended that functional measures
may assess for beneficiaries who do not
have the goal of improvement. Other
commenters noted that stabilization
measures are appropriate for quality
improvement initiatives as they closely
align with the goal of HH services to
help patients maintain their current
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level of function or when possible to
improve it. Another commenter
suggested closely monitoring functional
status measures to determine the impact
of other reforms, such as changes to the
payment approaches, to determine the
impact of these changes on patient
outcomes.
Response: We appreciate the
comments from MedPAC and others.
We agree that the maintenance of
function and avoidance or reduction in
functional decline are appropriate goals
for HH patients. We appreciate all
recommendations and will take these
comments into consideration as we
consider measures for future
rulemaking.
Comment: Three commenters
specifically supported the potentially
preventable within-stay hospitalization
measure. MedPAC supported the
development of a claims-based,
potentially preventable hospitalization
measure, adding that measuring
potentially preventable hospitalizations
holds providers accountable only for
conditions that generally could have
been managed by the HHA.
Response: We appreciate the
comments from MedPAC and others
pertaining to the potentially preventable
within-stay hospitalization measure
under consideration for future
implementation in the HH QRP. We
note that appropriately assessing
hospital readmissions as an outcome is
important, acknowledge the importance
of avoiding unintended consequences
that may arise from such assessments,
and will take into consideration the
commenters’ recommendations.
Comment: Commenters had
suggestions for other measures that
could be added to the HH QRP.
Response: We appreciate the
commenters’ recommendations and will
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take them into account in our future
measure development work.
1. IMPACT Act Implementation Update
As a result of the input and
suggestions provided by technical
experts at the TEPs held by our measure
developer, we noted in the proposed
rule that we are engaging in additional
development work for two measures
that will satisfy section 1899B(c)(1)(E) of
the Act, including performing
additional testing. We noted that we
intended to specify these measures
under section 1899B(c)(1)(E) of the Act
no later than January 1, 2019 and we
intend to propose to adopt them for the
CY 2021 HH QRP, with data collection
beginning on or about January 1, 2020.
We did not receive any comments on
this update.
H. Standardized Patient Assessment
Data
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1. Standardized Patient Assessment
Data Reporting for the CY 2019 HH QRP
Section 1895(b)(3)(B)(v)(IV)(bb) of the
Act requires that for calendar years
beginning on or after January 1, 2019,
HHAs submit to the Secretary
standardized patient assessment data
required under section 1899B(b)(1) of
the Act.
In the CY 2018 HH PPS proposed rule
(82 FR 35351) we proposed that the
current pressure ulcer measure,
Application of Percent of Residents or
Patients with Pressure Ulcers That Are
New or Worsened (Short Stay) (NQF
#0678), be replaced with the proposed
pressure ulcer measure, Changes in Skin
Integrity Post-Acute Care: Pressure
Ulcer/Injury, beginning with the CY
2020 HH QRP. The current pressure
ulcer measure will remain in the HH
QRP until that time. Accordingly, for
the requirement that HHAs report
standardized patient assessment data for
the CY 2019 HH QRP, we proposed that
the data elements used to calculate that
measure meet the definition of
standardized patient assessment data for
medical conditions and co-morbidities
under section 1899B(b)(1)(B)(iv) of the
Act, and that the successful reporting of
that data under section
1895(b)(3)(b)(v)(IV)(aa) of the Act for the
beginning of the HH episode (for
example, HH start of care/resumption of
care), as well as the end of the HH
episode (discharges) occurring during
the first two quarters of CY 2018 will
also satisfy the requirement to report
standardized patient assessment data
beginning with the CY 2019 HH QRP.
The collection of assessment data
pertaining to skin integrity, specifically
pressure related wounds, is important
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for multiple reasons. Clinical decision
making, care planning, and quality
improvement all depend on reliable
assessment data collection. Pressure
related wounds represent poor
outcomes, are a serious medical
condition that can result in death and
disability, are debilitating and painful,
and are often avoidable.94 95 96 97 98 99
Pressure related wounds are considered
healthcare acquired conditions.
As we noted, the data elements
needed to calculate the current pressure
ulcer measure are already included on
the OASIS data set and reported by
HHAs, and exhibit validity and
reliability for use across PAC providers.
Item reliability for these data elements
was also tested for the nursing home
setting during implementation of MDS
3.0. Testing results are from the RAND
Development and Validation of MDS 3.0
project.100 The RAND pilot test of the
MDS 3.0 data elements showed good
reliability and are applicable to the
OASIS because the data elements tested
are the same as those used in the OASIS
Data Set. Across the pressure ulcer data
elements, the average gold-standard
nurse to gold-standard nurse kappa
statistic was 0.905. The average goldstandard nurse to facility-nurse kappa
statistic was 0.937. Data elements used
to risk adjust this quality measure were
also tested under this same pilot test,
and the gold-standard to gold-standard
kappa statistic, or percent agreement
(where kappa statistic not available),
ranged from 0.91 to 0.99 for these data
elements. These kappa scores indicate
‘‘almost perfect’’ agreement using the
Landis and Koch standard for strength
of agreement.101
94 Casey, G. (2013). ‘‘Pressure ulcers reflect
quality of nursing care.’’ Nurs N Z 19(10): 20–24.
95 Gorzoni, M.L. and S.L. Pires (2011). ‘‘Deaths in
nursing homes.’’ Rev Assoc Med Bras 57(3): 327–
331.
96 Thomas, J.M., et al. (2013). ‘‘Systematic review:
Health-related characteristics of elderly
hospitalized adults and nursing home residents
associated with short-term mortality.’’ J Am Geriatr
Soc 61(6): 902–911.
97 White-Chu, E.F., et al. (2011). ‘‘Pressure ulcers
in long-term care.’’ Clin Geriatr Med 27(2): 241–258.
98 Bates-Jensen BM. Quality indicators for
prevention and management of pressure ulcers in
vulnerable elders. Ann Int Med. 2001;135 (8 Part 2),
744–51.
99 Bennet, G, Dealy, C Posnett, J (2004). The cost
of pressure ulcers in the UK, Age and Aging,
33(3):230–235.
100 Saliba, D., & Buchanan, J. (2008, April).
Development and validation of a revised nursing
home assessment tool: MDS 3.0. Contract No. 500–
00–0027/Task Order #2. Santa Monica, CA: Rand
Corporation. Retrieved from https://
www.cms.hhs.gov/NursingHomeQualityInits/
Downloads/MDS30FinalReport.pdf.
101 Landis, R., & Koch, G. (1977, March). The
measurement of observer agreement for categorical
data. Biometrics 33(1), 159–174.
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51731
The data elements used to calculate
the current pressure ulcer measure
received public comment on several
occasions, including when that measure
was proposed in the CY 2016 HH PPS
(80 FR 68623). Further, they were
discussed in the past by TEPs held by
our measure development contractor on
June 13 and November 15, 2013, and
recently by a TEP on July 18, 2016. TEP
members supported the measure and its
cross-setting use in PAC. The report,
Technical Expert Panel Summary
Report: Refinement of the Percent of
Patients or Residents with Pressure
Ulcers that are New or Worsened (ShortStay) (NQF #0678) Quality Measure for
Skilled Nursing Facilities (SNFs),
Inpatient Rehabilitation Facilities
(HHAs), Long-Term Care Hospitals
(LTCHs), and Home Health Agencies
(HHAs), is available at and https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/Post-Acute-Care-QualityInitiatives/IMPACT-Act-of-2014/
IMPACT-Act-Downloads-andVideos.html.
Comment: Some commenters
supported reporting the data elements
already implemented in the HH QRP to
fulfill the requirement to report
standardized patient assessment data for
the CY 2019 HH QRP. Specifically, the
commenters supported the use of data
elements used in calculation of the
Percent of Residents or Patients with
Pressure Ulcers That Are New or
Worsened (Short Stay) (NQF #0678) to
fulfill this requirement. However, one
commenter recommended that CMS
implement such measures after public
deliberation and discussion. A
commenter suggested that CMS adopt
the same policies in this CY 2018 HH
PPS final rule as it adopted for IRFs,
SNFs and LTCHs in the other final rules
issued this year.
Response: We appreciate the support
and where possible we have aligned
with the other settings. We affirm that
as we continue to implement measures,
such as the pressure ulcer quality
measure, we will continue to engage the
public both during the measure
development phase and through the
rulemaking process.
Final Decision: After consideration of
the public comments received, we are
finalizing as proposed that the data
elements currently reported by HHAs to
calculate the current measure, Percent
of Residents or Patients with Pressure
Ulcers That Are New or Worsened
(Short Stay) (NQF #0678),to meet the
definition of standardized patient
assessment data with respect to medical
conditions and co-morbidities under
section 1899B(b)(1)(B)(iv) of the Act,
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and that the successful reporting of that
data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will
also satisfy the requirement to report
standardized patient assessment data
under section 1895(b)(3)(B)(v)(IV)(bb) of
the Act beginning with the CY 2019 HH
QRP.
2. Standardized Patient Assessment
Data Reporting Beginning With the CY
2020 HH QRP
In the CY 2018 HH PPS proposed rule
(82 FR 35355 through 35371), we
described our proposals for the
reporting of standardized patient
assessment data by HHAs beginning
with the CY 2020 HH QRP. LTCHs,
IRFs, and SNFs are also required to
report standardized patient assessment
data through their applicable PAC
assessment instruments, and they do so
by responding to identical assessment
questions developed for their respective
settings using an identical set of
response options (which incorporate an
identical set of definitions and
standards). We proposed that HHAs will
be required to report these data at
admission (SOC/ROC) and discharge
beginning on January 1, 2019, with the
exception of three data elements (Brief
Interview of Mental Status (BIMS),
Hearing, and Vision) that will be
required at SOC/ROC only. Following
the initial reporting year (which will be
based on 6 months of data) for the CY
2020 HH QRP, subsequent years for the
HH QRP would be based on a full
calendar year of such data reporting.
In selecting the data elements, we
carefully weighed the balance of burden
in assessment-based data collection and
aimed to minimize additional burden
through the utilization of existing data
in the assessment instruments. We also
noted that the patient and resident
assessment instruments are considered
part of the medical record and sought
the inclusion of data elements relevant
to patient care.
We also took into consideration the
following factors for each data element:
overall clinical relevance; ability to
support clinical decisions, care
planning, and interoperable exchange to
facilitate care coordination during
transitions in care; and the ability to
capture medical complexity and risk
factors that can inform both payment
and quality. In addition, the data
elements had to have strong scientific
reliability and validity; be meaningful
enough to inform longitudinal analysis
by providers; had to have received
general consensus agreement for its
usability; and had to have the ability to
collect such data once but support
multiple uses. Further, to inform the
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final set of data elements for proposal,
we took into account technical and
clinical subject matter expert review,
public comment, and consensus input
in which such principles were applied.
We received several comments related
to the reporting of the standardized
patient assessment data.
Comment: Many commenters
expressed significant concerns with
respect to our standardized patient
assessment data proposals. Several
commenters stated that the new
standardized patient assessment data
reporting requirements will impose
significant burden on providers, given
the volume of new standardized patient
assessment data elements that we
proposed to add to the OASIS. Several
commenters noted that the addition of
the proposed standardized patient
assessment data elements will require
hiring more staff, retraining staff on
revised questions or coding guidance,
and reconfiguring internal databases
and EHRs. Other commenters expressed
concerns about the gradual but
significant past and future expansion of
the OASIS through the addition of
standardized patient assessment data
elements and quality measures, noting
the challenge of coping with ongoing
additions and changes.
Several commenters expressed
concern related to the implementation
timeline in the proposed rule. Several
commenters noted that CMS had not yet
provided sufficient specifications or
educational materials to support
implementation of the new patient
assessments in the proposed timeline. A
few commenters urged CMS to delay the
reporting of new standardized patient
assessment data elements and to
carefully assess whether all of the
proposed standardized patient
assessment data elements are necessary
under the IMPACT Act.
Response: We understand the
concerns raised by commenters that
finalizing our standardized patient
assessment data proposals will require
HHAs to spend a significant amount of
resources preparing to report the data,
including updating relevant protocols
and systems and training appropriate
staff. We also recognize that we can
meet our obligation to require the
reporting of standardized patient
assessment data for the categories
described in section 1899B(b)(1)(B) of
the Act while simultaneously being
responsive to these concerns. Therefore,
after consideration of the public
comments we received on these issues,
we have decided that at this time, we
will not finalize the standardized
patient assessment data elements we
proposed for three of the five categories
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under section 1899B(b)(1)(B) of the Act:
Cognitive Function and Mental Status;
Special Services, Treatments, and
Interventions; and Impairments.
Although we believe that the
proposed standardized patient
assessment data elements would
promote transparency around quality of
care and price as we continue to explore
reforms to the PAC payment system, the
data elements that we proposed for each
of these categories would have imposed
a new reporting burden on HHAs. We
agree that it would be useful to evaluate
further how to best identify the
standardized patient assessment data
that would satisfy each of these
categories; would be most appropriate
for our intended purposes including
payment and measure standardization;
and can be reported by HHAs in the
least burdensome manner. As part of
this effort, we intend to conduct a
national field test that allows for
stakeholder feedback and to consider
how to maximize the time HHAs have
to prepare for the reporting of
standardized patient assessment data in
these categories. We intend to make new
proposals for the categories described in
sections 1899B(b)(1)(B)(ii), (iii) and (v)
of the Act no later than in the CY 2020
HH PPS proposed rule.
In this final rule, we are finalizing the
standardized patient assessment data
elements that we proposed to adopt for
the IMPACT Act categories of
Functional Status and Medical
Conditions and Co-Morbidities. Unlike
the standardized patient assessment
data that we are not finalizing, the
standardized patient assessment data
that we proposed for Medical
Conditions Co-Morbidities category is
already required to calculate the Percent
of Residents or Patients with Pressure
Ulcers That Are New or Worsened (NQF
#0678) quality measure, and the
Changes in Skin Integrity Post-Acute
Care: Pressure Ulcer/Injury quality
measure. We are finalizing the quality
measure, Application of Percent of
Long-Term Care Hospital Patients with
an Admission and Discharge Functional
Assessment and a Care Plan That
Addresses Function (NQF #2631), and
the additional standardized patient
assessment data elements in Section GG
to satisfy the category of Functional
Status.
Comment: Some commenters
expressed support for the adoption of
standardized patient assessment data
elements. Several of these commenters
expressed support for standardizing the
definitions as well as the
implementation of the data collection
effort. A few commenters also supported
CMS’ goal of standardizing the
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questions and responses across all PAC
settings. Another commenter approved
of the efforts CMS is making to engage
the PAC community on the
implementation of the IMPACT Act,
including holding Special Open Door
Forums and Medicare Learning Network
(MLN) Calls to communicate with
providers about expectations/timelines
over five years. MedPAC recognized the
value of and need for a unified patient
assessment system for PAC as part of a
potential unified payment system for
PAC.
Response: We appreciate the support.
Comment: A few commenters stated
that there is insufficient evidence
demonstrating the reliability and
validity of the proposed standardized
patient assessment data elements.
Several commenters stated that the
expanded standardized patient
assessment data reporting requirements
have not yet been adequately tested to
ensure they collect accurate and useful
data in the HHA setting.
Response: Our standardized patient
assessment data elements were selected
based on a rigorous multistage process
described in the CY 2018 HH PPS
proposed rule (82 FR 35344). In
addition, we believe that the PAC PRD
testing of many of these data elements
provides good evidence from a large,
national sample of patients and
residents in PAC settings to support the
use of these standardized patient
assessment data elements in and across
PAC settings. However, as previously
explained, we have decided at this time
not to finalize the proposals for three of
the five categories under section
1899B(b)(1)(B) of the Act: Cognitive
Function and Mental Status; Special
Services, Treatments, and Interventions;
and Impairments. Prior to making new
proposals for these categories, we intend
to conduct additional testing to ensure
that the standardized patient assessment
data elements we select are reliable,
valid and appropriate for their intended
use.
Comment: MedPAC suggested that
CMS should be mindful that some data
elements, when used for risk
adjustment, may be susceptible to
provider manipulation. MedPAC is
concerned about the proposed elements
such as oxygen therapy, intravenous
medications, and nutritional approaches
that may incentivize increased use of
services. MedPAC supported the
inclusion of these care items when they
are tied to medical necessity, such as in
previous MedPAC work, where patients
were counted as using oxygen services
only if they have diagnoses that
typically require the use of oxygen.
MedPAC encouraged CMS to take a
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similar approach in measuring use of
services that are especially
discretionary. For some data elements,
MedPAC suggested that CMS consider
requiring a physician to attest that the
reported service was reasonable and
necessary and include a statement
adjacent to the signature line warning
that filing a false claim is subject to
treble damages under the False Claims
Act.
Response: We thank MedPAC for their
support of the standardized patient
assessment data elements that are
associated with medical necessity. We
appreciate their suggestions to mitigate
the potential for false data submission
and the unintended consequence of use
of services that are not medically
indicated.
Comment: While supporting the
overall concept of standardization
across PAC settings, several commenters
strongly believed that the home health
setting is different than institutional
settings and urged CMS to consider this.
One of these commenters encouraged
CMS to perform testing specifically in
the home health setting. Another
commenter was concerned about the use
of some data elements because they
were not designed for the home health
setting and require specialized training
to accurately administer. Several
commenters emphasized the importance
of risk adjustment, with some stating
that effective risk adjustment will be an
essential policy feature for home health
agencies to distinguish how patients
and data collection in non-standardized
settings such as the beneficiary’s home
differ from institutional settings.
Response: We acknowledge that the
four PAC provider types each have
unique challenges and provide unique
services and appreciate the commenters’
concerns specific to the home health
setting and the potential variation in
services and populations. Because of
this, we conducted a thorough process
of phased testing and stakeholder
consensus to ensure we considered
items that are aligned across PAC
settings and are relevant to and feasible
in each setting. However, for the reasons
previously explained, we have decided
at this time not to finalize the
standardized patient assessment data
elements we proposed for three of the
five categories under section
1899B(b)(1)(B) of the Act.
A full discussion of the standardized
patient assessment data elements that
we proposed to adopt for the categories
described in sections 1899B(b)(1)(B)(ii),
(iii) and (v) of the Act can be found in
the CY 2018 HH PPS proposed rule (82
FR 35355 through 35371). In light of our
decision not to finalize our proposals
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51733
with respect to these categories, we are
not going to address in this final rule the
specific technical comments that we
received on these proposed
standardized patient assessment data
elements. However, we appreciate the
many technical comments we did
receive specific to each of these data
elements, and we will take them into
consideration as we develop new
proposals for these categories. In this
section, we discuss the comments we
received specific to the standardized
patient assessment data we proposed to
adopt and are finalizing in this final
rule, for the categories of Functional
Status and Medical Conditions and CoMorbidities.
3. Standardized Patient Assessment
Data by Category
a. Functional Status Data
We proposed that the data elements
that will be reported by HHAs to
calculate the measure, Application of
Percent of Long-Term Care Hospital
Patients with an Admission and
Discharge Functional Assessment and a
Care Plan That Addresses Function
(NQF #2631), as described in section
V.F.2 of the proposed rule will also
meet the definition of standardized
patient assessment data for functional
status under section 1899B(b)(1)(B)(i) of
the Act, and that the successful
reporting of that data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will
also satisfy the requirement to report
standardized patient assessment data
under section 1895(b)(3)(B)(v)(IV)(bb) of
the Act. Details on the data used to
calculate this measure is discussed in
section V.F.2. of this final rule.
To further satisfy the requirements
under section 1899B(b)(1)(B)(i) of the
Act and specifically our efforts to
achieve standardized patient assessment
data pertaining to functional status,
such as mobility and self-care at
admission to a PAC provider and before
discharge from a PAC provider, we also
proposed to adopt the functional status
data elements that specifically address
mobility and self-care as provided in the
Act. We noted that these data elements
were also used to calculate the function
outcome measures implemented and/or
proposed for implementation in three
other post-acute quality reporting
programs to which the IMPACT Act
applies (Application of NQF #2633—
Change in Self-Care Score for Medical
Rehabilitation Patients; Application of
NQF #2634—Change in Mobility Score
for Medical Rehabilitation Patients;
Application of NQF #2635—Discharge
Self-Care Score for Medical
Rehabilitation Patients; and Application
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of NQF #2636—Discharge Mobility
Score for Medical Rehabilitation
Patients).
To achieve standardization, we noted
that we have implemented such data
elements, or sub-sets of the items, into
the other post-acute care patient/
resident assessment instruments and we
proposed that they also meet the
definition of standardized patient
assessment data for functional status
under section 1899B(b)(1)(B)(i) of the
Act, and that the successful reporting of
such data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will
also satisfy the requirement to report
standardized patient assessment data
under section 1895(b)(3)(B)(v)(IV)(bb) of
the Act. These data elements currently
are collected in the Section GG:
Functional Abilities and Goals located
in current versions of the MDS and the
IRF–PAI assessment instruments.
As previously described, the patient
assessment data that assess for
functional status are from the CARE
Item Set. They were specifically
developed for cross-setting application
and are the result of consensus building
and public input. Further, we received
public comment and input on these
patient assessment data. Their reliability
and validity testing were conducted as
part of CMS’ Post-Acute Care Payment
Reform Demonstration, and we
concluded that the functional status
items have acceptable reliability and
validity. We referred the reader to
section V.F.2 of the proposed rule for a
full description of the CARE Item Set
and description of the testing
methodology and results that are
available in several reports. For more
information about this quality measure
and the data elements used to calculate
it, we referred readers to the FY 2016
IPPS/LTCH PPS final rule (80 FR 49739
through 49747), the FY 2016 IRF PPS
final rule (80 FR 47100 through 47111),
and the FY 2016 SNF PPS final rule (80
FR 46444 through 46453).
Therefore, we proposed to adopt the
functional status data elements for the
CY 2020 HH QRP, requiring HHAs to
report these data starting on January 1,
2019. We noted that this proposal
would align with the required reporting
timeframe for the CY 2020 HH QRP.
Following the initial 2 quarters of
reporting for the CY 2020 HH QRP, we
proposed that for subsequent years for
the HH QRP, the reporting of
standardized patient assessment data
would be based on 12 months of data
reporting beginning with July 1, 2019,
through June 30, 2020 for the CY 2021
HH QRP.
Comment: Several commenters,
including MedPAC, supported the
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collection of standardized patient
assessment data across PAC settings.
Some commenters specifically
addressed support for CMS’ proposal
that data elements submitted to CMS to
calculate the measure, Application of
Percent of Long-Term Care Hospital
Patients with an Admission and
Discharge Functional Assessment and a
Care Plan that Addresses Function (NQF
#2631), would also satisfy the
requirement to report standardized
patient assessment data elements under
section 1899B(b)(1)(B)(i) of the Act
addressing functional status, such as
mobility and self-care at admission to a
PAC provider and before discharge from
a PAC provider.
Response: We appreciate the
commenters’ support.
Comment: A commenter suggested
that CMS use the functional assessment
item, GG0170C: Lying to sitting on the
side of bed for purposes of
standardization.
Response: We do not believe that
collecting only GG170C would be
sufficient for purposes of collecting
standardized function data. We need a
larger subset of Section GG items to
calculate one of the measures that we
are finalizing in this final rule,
Application of Percent of Long-Term
Care Hospital Patients with an
Admission and Discharge Functional
Assessment and a Care Plan That
Addresses Function (NQF #2631),
which is already finalized for SNFs,
LTCHs and IRFs. Section GG in its
entirety also meets the definition of
standardized patient assessment data
with respect to function because it is
standardized across the four PAC
settings. If we did not collect Section
GG in its entirety from HHAs, we would
be collecting a different set of function
items from HHAs than we collect from
other PAC provider types.
Final Decision: After consideration of
the public comments received, we are
finalizing that the data elements in
Section GG: Functional Abilities and
Goals meet the definition of
standardized patient assessment data
elements for functional status under
section 1899B(b)(1)(B)(i) of the Act,
specifically those Section GG
standardized patient assessment data
elements that are used in the quality
measure, ‘‘Percent of Long-Term Care
Hospital Patients with an Admission
and Discharge Functional Assessment
and a Care Plan that Addresses Function
(NQF #2631)’’, and the additional
standardized functional status data
elements in Section GG. We note that
Section GG includes item GG170Q,
which we inadvertently omitted in the
specifications that accompanied the CY
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2018 HH PPS proposed rule. The
Section GG data elements can be found
in the Finalized Specifications for HH
QRP Quality Measures and
Standardized Patient Assessment Data
Elements document available at: https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HHQIQualityMeasures.html. We are
also finalizing that the data elements
needed to calculate the measure,
Application of Percent of Long-Term
Care Hospital Patients with an
Admission and Discharge Functional
Assessment and a Care Plan That
Addresses Function (NQF #2631), meet
the definition of standardized patient
assessment data elements for functional
status under section 1899B(b)(1)(B)(i) of
the Act, and that the successful
reporting of that data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will
also satisfy the requirement to report
standardized patient assessment data
elements under section
1895(b)(3)(B)(v)(IV)(bb) of the Act.
b. Medical Condition and Comorbidity
Data
We proposed that the data elements
needed to calculate the current measure,
Percent of Residents or Patients with
Pressure Ulcers That Are New or
Worsened (Short Stay) (NQF #0678),
and that the proposed measure, Changes
in Skin Integrity Post-Acute Care:
Pressure Ulcer/Injury, meet the
definition of standardized patient
assessment data element with respect to
medical conditions and co-morbidities
under section 1899B(b)(1)(B)(iv) of the
Act, and that the successful reporting of
that data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will
also satisfy the requirement to report
standardized patient assessment data
under section 1895(b)(3)(B)(v)(IV)(bb) of
the Act.
‘‘Medical conditions and comorbidities’’ and the conditions
addressed in the standardized
assessment patient data elements used
in the calculation and risk adjustment of
these measures, that is, the presence of
pressure ulcers, diabetes, incontinence,
peripheral vascular disease or
peripheral arterial disease, mobility, as
well as low body mass index (BMI), are
all health-related conditions that
indicate medical complexity that can be
indicative of underlying disease severity
and other comorbidities.
Specifically, the data elements used
in the measure are important for care
planning and provide information
pertaining to medical complexity.
Pressure ulcers are serious wounds
representing poor outcomes, and can
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result in sepsis and death. Assessing
skin condition, care planning for
pressure ulcer prevention and healing,
and informing providers about their
presence in patient transitions of care
are a customary and best practice.
Venous and arterial disease and diabetes
are associated with insufficient low
blood flow, which may increase the risk
of tissue damage. These diseases
commonly are indicators of factors that
may place individuals at risk for
pressure ulcer development and are
therefore important for care planning.
Low BMI, which may be an indicator of
underlying disease severity, may be
associated with loss of fat and muscle,
resulting in potential risk for pressure
ulcers due to shearing. Bowel
incontinence, and the possible
maceration to the skin associated, can
lead to higher risk for pressure ulcers.
In addition, the bacteria associated with
bowel incontinence can complicate
current wounds and cause local
infection. Mobility is an indicator of
impairment or reduction in mobility
and movement which is a major risk
factor for the development of pressure
ulcers. These data elements are
important for care planning, transitions
in services and identifying medical
complexities.
Comment: Commenters supported our
proposal to use data elements already
implemented in the HH QRP to satisfy
the requirement to report standardized
patient assessment data.
Response: We appreciate the support.
Final decision: After consideration of
the public comments received, we are
finalizing as proposed that the data
elements currently reported by HHAs to
calculate the current measure, Percent
of Residents or Patients with Pressure
Ulcers That Are New or Worsened
(Short Stay) (NQF #0678), and the
finalized measure, Changes in Skin
Integrity Post-Acute Care: Pressure
Ulcer/Injury, meet the definition of
standardized patient assessment data for
medical conditions and co-morbidities
under section 1899B(b)(1)(B)(iv) of the
Act, and that the successful reporting of
that data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will
also satisfy the requirement to report
standardized patient assessment data
under section 1895(b)(3)(B)(v)(IV)(bb) of
the Act.
We note that for purposes of meeting
the requirements of the CY 2020 HH
QRP, HHAs will be required to report
the data elements needed to calculate
the current pressure ulcer measure for
the last two quarters of CY 2018 (July–
December) and the data elements
needed to calculate the updated
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pressure ulcer measure for the first two
quarters of CY 2019 (January–June).
I. Form, Manner, and Timing of Data
Submission Under the HH QRP
1. Start Date for Reporting Standardized
Patient Assessment Data by New HHAs
In the CY 2016 HH PPS final rule (80
FR 68703 through 68706), we adopted
timing for new HHAs to begin reporting
data on quality measures under the HH
QRP. In the CY 2018 HH PPS proposed
rule (82 FR 35371), we proposed that
new HHAs would be required to begin
reporting standardized patient
assessment data on the same schedule.
Comment: One commenter supported
our proposed policy to require that new
HHAs begin reporting standardized
patient assessment data on the same
schedule that they are required to begin
reporting data on quality measures.
Response: We thank the commenter
for the support.
Final Decision: After consideration of
the comments we received, we are
finalizing our proposal that new HHAs
will be required to begin reporting
standardized patient assessment data on
the same schedule that they are
currently required to begin reporting
other quality data under the HH QRP.
2. Mechanism for Reporting
Standardized Patient Assessment Data
Beginning With the CY 2019 HH QRP
Under our current policy, HHAs
report data by completing applicable
sections of the OASIS, and submitting
the OASIS to CMS through the QIES,
ASAP system. For more information on
HH QRP reporting through the QIES
ASAP system, we referred readers to
https://www.qtso.com/index.php. In
addition to the data currently submitted
on quality measures as previously
finalized and described in Table 18 of
this rule, in the CY 2018 HH PPS
proposed rule (82 FR 35372), we
proposed that HHAs would be required
to begin submitting the proposed
standardized patient assessment data for
HHA Medicare and Medicaid quality
episodes that begin or end on or after
January 1, 2019 using the OASIS.
Further, we proposed that all
standardized patient assessment data
elements would be collected at SOC/
ROC using the OASIS item set, and all
except the Brief Interview for Mental
Status (BIMS), Hearing, and Vision data
elements are or would be collected at
discharge using the OASIS item set.
Details on the modifications and
assessment collection for the OASIS for
the proposed standardized data are
available at https://www.cms.gov/
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Medicare/Quality-Initiatives-PatientAssessment-Instruments/
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HHQIQualityMeasures.html.
We invited public comment on these
proposals.
Comment: We received a comment in
support of the proposed mechanisms for
reporting standardized patient
assessment in the same manner as the
quality measure data for assessment
based data beginning with the CY 2019
HH QRP.
Response: We thank the commenter
for its support.
Final Decision: After consideration of
the public comment received, we are
finalizing our policy as proposed to use
the same data reporting mechanism for
the submission of the standardized
patient assessment data elements that is
already used for reporting quality
measure data used in the HH QRP
beginning with the CY 2019 HH QRP.
3. Schedule for Reporting Standardized
Patient Assessment Data Beginning
With the CY 2019 HH QRP
In the CY 2018 HH PPS proposed rule
(82 FR 35372) we proposed to apply our
current schedule for the reporting of
measure data to the reporting of
standardized patient assessment data,
beginning with the CY 2019 HH QRP.
Under that policy, except for the first
program year for which a measure is
adopted, HHAs must report data on
measures for HHA Medicare and
Medicaid quality episodes that occur
during the 12-month period (between
July 1 and June 30) that applies to the
program year. For the first program year
for which a measure is adopted, HHAs
are only required to report data on HHA
Medicare and Medicaid quality episodes
that begin on or after January 1 and end
up to and including June 30 of the
calendar year that applies to that
program year. For example, for the CY
2019 HH QRP, data on measures
adopted for earlier program years must
be reported for all HHA Medicare and
Medicaid quality episodes that begin on
or after July 1, 2017, and end on or
before June 30, 2018. However, data on
new measures adopted for the first time
for the CY 2019 HH QRP program year
must only be reported for HHA
Medicare and Medicaid quality episodes
that begin or end during the first two
quarters of CY 2018. Tables 20 and 21
illustrate this policy and its proposed
application to the reporting of
standardized patient assessment data,
using CY 2019 and CY 2020 as
examples.
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TABLE 20—SUMMARY ILLUSTRATION OF INITIAL REPORTING FOR NEWLY ADOPTED MEASURES AND PROPOSED
STANDARDIZED PATIENT ASSESSMENT DATA REPORTING USING CY Q1 AND Q2 DATA FOR THE HH QRP *
Proposed data submission deadlines beginning with CY 2019 HH
QRP *
Proposed data collection/submission reporting period *
January 1, 2018–June 30, 2018. .............................................................
July 31, 2018.
* We note that submission of the OASIS must also adhere to the HH PPS deadlines.
¥ The term ‘‘CY 2019 HH QRP’’ means the calendar year for which the HH QRP requirements applicable to that calendar year must be met in
order for a HHA to avoid a two percentage point reduction to its market basket percentage when calculating the payment rates applicable to it for
that calendar year.
TABLE 21—SUMMARY ILLUSTRATION OF OASIS 12 MONTH DATA REPORTING FOR MEASURES AND PROPOSED
STANDARDIZED PATIENT ASSESSMENT DATA REPORTING FOR THE HH QRP *
Proposed data submission deadlines beginning with CY 2020 HH
QRP * ∧
Proposed data collection/submission reporting period *
July 1, 2018–June 30, 2019. ....................................................................
July 31, 2019.
* We note that submission of the OASIS must also adhere to the HH PPS deadlines.
∧ The term ‘‘CY 2020 HH QRP’’ means the calendar year for which the HH QRP requirements applicable to that calendar year must be met in
order for a HHA to avoid a two percentage point reduction to its market basket percentage when calculating the payment rates applicable to it for
that calendar year.
We invited comment on our proposal
to extend our current policy governing
the schedule for reporting the quality
measure data to the reporting of
standardized patient assessment data for
the HH QRP beginning with the CY
2019 HH QRP.
We did not receive any comments
regarding this proposal.
Final Decision: We are finalizing our
proposal as proposed to extend our
current policy governing the schedule
for reporting the quality measure data to
the reporting of standardized patient
assessment data for the HH QRP
beginning with the CY 2019 HH QRP.
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4. Schedule for Reporting Quality
Measures Beginning With the CY 2020
HH QRP
As discussed in section V.I. of this
final rule, we are finalizing the adoption
of three quality measures beginning
with the CY 2020 HH QRP: Changes in
Skin Integrity Post-Acute Care: Pressure
Ulcer/Injury; Application of The Percent
of Residents Experiencing One or More
Falls with Major Injury (NQF #0674);
and Application of Percent of LongTerm Care Hospital Patients with an
Admission and Discharge Functional
Assessment and a Care Plan That
Addresses Function (NQF #2631). In the
CY 2018 HH PPS proposed rule (82 FR
35372), we proposed that HHAs would
report data on these measures using
OASIS reporting that is submitted
through the QIES ASAP system. More
information on OASIS reporting using
the QIES ASAP system is located at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/OASIS/
DataSpecifications.html.
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For the CY 2020 HH QRP, under our
current policy HHAs will be required to
report these data for HHA Medicare and
Medicaid quality episodes that begin or
end during the period from January 1,
2019, to June 30, 2019. Beginning with
the CY 2021 HH QRP, we proposed that
HHAs would will be required to submit
data for the entire 12-month period from
July 1 to June 30. Further, for the
purposes of measure calculation, our
policy was established in the CY 2017
HH PPS final rule (81 FR76784) that
data are utilized using calendar year
timeframes with review and correction
periods.
Comment: A commenter supported
the proposed schedule for reporting the
three new quality measures beginning
with the CY 2020 QRP. However, the
commenter also suggested that there is
a disparity in how home health
providers are reimbursed, which creates
challenges for their submission of the
required data.
Response: We interpret the comment
to be suggesting that Medicare
reimbursement rates for HH services,
compared to Medicare rates for postacute care services furnished by
different provider-types, may affect the
ability of HHAs to comply with the data
reporting requirements under the HH
QRP. We are cognizant of the challenges
of data collection and we consider this
when developing and adopting our
measures.
Final Decision: After consideration of
the public comment received, we are
finalizing our policy as proposed for the
Schedule for Reporting the Quality
Measures beginning with the CY 2020
HH QRP.
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5. Input Sought for Data Reporting
Related to Assessment Based Measures
We have received input suggesting
that we expand the population for
quality measurement to include all
patients regardless of payer.
Approximately 75 percent of home
health expenditures in 2014 were made
by either Medicare or Medicaid and
currently both Medicare and Medicaid
collect and report data for OASIS. We
believe that expanding the patient
population for which OASIS collects
data will allow us to ensure data that is
representative of quality provided to all
patients in the HHA setting, and
therefore, allow us to better determine
whether HH Medicare beneficiaries
receive the same quality of care that
other patients receive. We also
appreciate that collecting quality data
on all patients regardless of payer
source may create additional burden.
However, we have also received input
that the effort to separate out Medicare
and Medicaid beneficiaries, who are
currently reported through OASIS, from
other patients, creates clinical and work
flow implications with an associated
burden too, and noted that we further
appreciate that it is common practice for
HHAs to collect OASIS data on all
patients, regardless of payer source.
Thus, we sought input on whether we
should require quality data reporting on
all HH patients, regardless of payer,
where feasible—noting that because
Medicare Part A claims data are
submitted only with respect to Medicare
beneficiaries, claims-based measures
would continue to be calculated only for
Medicare beneficiaries. We would like
to clarify that CMS sought comment on
this all payor topic and therefore there
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is no proposed policy to finalize. We
appreciate the comments received and
will take all recommendations into
consideration.
Comment: Several commenters
supported data collection on all patients
regardless of payor. One commenter
requested that CMS provide additional
explanation of what the benefit would
be to collecting OASIS data on all
patients regardless of payor. Several
commenters stated that the addition of
OASIS reporting for all patients
regardless of payor will impose
significant burden on HHAs. Some
commenters noted that they used
separate assessment documents for
patients who are insured by private
payors and that they used these
assessments, in part, to avoid the
burden of OASIS. A few commenters
suggested that the collection of OASIS
data on all patients regardless of payor
could result in healthcare professionals
spending more time with
documentation and less time providing
patient care. Some commenters
suggested that if CMS requires HHAs to
submit OASIS assessments on all
patients, they might need to increase
their staff hours, hire additional staff
and incur additional expenses.
Response: We continue to believe that
the reporting of all-payor data under the
HH QRP would add value to the
program and provide a more accurate
representation of the quality provided
by HHAs. Although we acknowledge the
concerns raised by commenters
regarding the potential burden of
reporting all-payer data and on the
potential impact of such a requirement
for the HH QRP, we wish to clarify that
under the HH Conditions of
Participation (42 CFR 484.55), each
patient must receive, and an HHA must
provide, a patient-specific,
comprehensive assessment that
accurately reflects the patient’s current
health status and includes information
that may be used to demonstrate the
patient’s progress toward achievement
of desired outcomes. The
comprehensive assessment must also
incorporate the use of the current
version of the OASIS items, using the
language and groupings of the OASIS
items, as specified by the Secretary.
Comment: We received several
comments pertaining to the submission
requirements of the OASIS instrument.
Some commenters suggested that OASIS
data was required for submission on
only Medicare fee-for-service
beneficiaries, while other commenters
stated that HHAs must complete the
OASIS for all Medicare and Medicaid
patients. Another commenter noted that
the HH Conditions of Participation
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already apply to all patients in a
Medicare-certified HHA. Other
commenters stated that they did not
know what patient populations must be
given an OASIS assessment.
Response: As previously discussed,
for the purposes HH QRP, data reporting
on the OASIS includes all Medicare and
Medicaid beneficiaries. However, the
comprehensive assessment must also
incorporate the collection of the current
version of the OASIS items, using the
language and groupings of the OASIS
items.
Comment: Several commenters stated
concerns about the potential impact of
all-payor information on the HH QRP
public reporting and on the HHVBP
model because private payors differ
from CMS with regard to care pathways,
approval, and authorization processes.
Some commenters stated that private
payors had proprietary information and
that CMS would exceed its authority if
it required all-payor reporting.
Commenters also stated that some
private insurers had different
requirements than CMS pertaining to
the number of visits paid for by such
insurers, which would inhibit the
agency in comparing performance
across HHAs.
Response: We acknowledge concerns
raised for the HHVBP model and the
potential downstream impacts. With
regard to the commenter suggesting that
private payors’ patients would generate
proprietary information, we want to
clarify that the OASIS is not a
proprietary instrument and therefore we
do not believe that a requirement that
HHAs use the OASIS in compliance
with our CoPs raises proprietary issues.
J. Other Provisions for the CY 2019 HH
QRP and Subsequent Years
1. Application of the HH QRP Data
Completion Thresholds to the
Submission of Standardized Patient
Assessment Data Beginning With the CY
2019 HH QRP
In the CY 2016 HH PPS final rule (80
FR 68703 through 68704), we defined
the pay-for-reporting performance
system model that could accurately
measure the level of an HHA’s
submission of OASIS data based on the
principle that each HHA is expected to
submit a minimum set of two matching
assessments for each patient admitted to
their agency. These matching
assessments together create what is
considered a quality episode of care,
consisting ideally of a SOC or ROC
assessment and a matching End of Care
EOC assessment. EOC assessments
comprise the Discharge from Agency,
Death at Home and Transfer to an
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51737
Inpatient Facility time points. For
further information on successful
submission of OASIS assessments, types
of assessments submitted by an HHA
that fit the definition of a quality
assessment, defining the ‘‘Quality
Assessments Only’’ (QAO) formula, and
implementing a pay-for-reporting
performance requirement over a 3-year
period, please see the CY 2016 HH PPS
final rule (80 FR 68704 to 68705).
Additionally, we finalized the payfor-reporting threshold requirements in
the CY 2016 HH PPS final rule. We
finalized a policy through which HHAs
must score at least 70 percent on the
QAO metric of pay-for-reporting
performance requirement for CY 2017
(reporting period July 1, 2015, to June
30, 2016), 80 percent for CY 2018
(reporting period July 1, 2016, to June
30, 2017) and 90 percent for CY 2019
(reporting period July 1, 2017, to June
30, 2018). An HHA that does not meet
this requirement for a calendar year will
be subject to a two percentage point
reduction to the market basket
percentage increase that will otherwise
apply for that calendar year. In the CY
2018 HH PPS proposed rule (82 FR
35373), we proposed to apply the
threshold requirements established in
the CY 2016 HH PPS rule to the
submission of standardized patient
assessment data beginning with the CY
2019 HH QRP.
Comment: Commenter provided
feedback on the QAO standard which
requires that at least 90 percent of
OASIS assessments be usable for
calculating quality measures or be
subject to a 2-percentage point
reduction to the market basket update
for CY 2019. One commenter agreed
with our proposal to apply the HH QRP
data completion thresholds to the
submission of standardized patient
assessment data beginning in the CY
2019 HH QRP. A commenter suggested
that the proposed 90 percent threshold
is very high and may be difficult for
small or rural providers meet, and
suggested changing this to 80 percent or
higher.
Response: We disagree that the 90
percent threshold for CY 2019 is too
high or difficult for HHAs to meet.
The home health CoPs as codified (42
CFR 484.55) mandate use of the OASIS
data set. OASIS reporting was first
implemented on July 19, 1999 and in
2007, we adopted mandatory OASIS
reporting for quality reporting purposes
under section 1895(b)(3)(B)(v)(I) of the
Act. Furthermore, HHAs have been
required to submit OASIS data as a
condition of payment of their Medicare
claims since 2010. Since, HHAs have
been required to report OASIS data for
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the last 18 years as a CoP in the
Medicare program and as a condition of
payment of their Medicare claims for
the past 7 years, our establishment of a
90 percent threshold for OASIS
reporting should not place any new or
additional burden on HHAs.
Final Decision: After consideration of
the comments received, we are
finalizing our proposal as proposed to
extend our current HH QRP data
completion requirements to the
submission of standardized patient
assessment data.
2. HH QRP Submission Exception and
Extension Requirements
Our experience with other QRPs has
shown that there are times when
providers are unable to submit quality
data due to extraordinary circumstances
outside their control (for example,
natural, or man-made disasters). Other
extenuating circumstances are reviewed
on a case-by-case basis. In the CY 2018
HH QRP proposed rule (82 FR 35373),
we proposed to define a ‘‘disaster’’ as
any natural or man-made catastrophe
which causes damages of sufficient
severity and magnitude to partially or
completely destroy or delay access to
medical records and associated
documentation. Natural disasters could
include events such as hurricanes,
tornadoes, earthquakes, volcanic
eruptions, fires, mudslides, snowstorms,
and tsunamis. Man-made disasters
could include such events as terrorist
attacks, bombings, floods caused by
man-made actions, civil disorders, and
explosions. A disaster may be
widespread and impact multiple
structures or be isolated and impact a
single site only.
In certain instances of either natural
or man-made disasters, an HHA may
have the ability to conduct a full patient
assessment and record and save the
associated data either during or before
the occurrence of the extraordinary
event. In this case, the extraordinary
event has not caused the agency’s data
files to be destroyed, but it could hinder
the HHA’s ability to meet the QRP’s data
submission deadlines. In this scenario,
the HHA will potentially have the
ability to report the data at a later date,
after the emergency has passed. In such
cases, a temporary extension of the
deadlines for reporting might be
appropriate.
In other circumstances of natural or
man-made disaster, an HHA may not
have had the ability to conduct a full
patient assessment, or to record and
save the associated data before the
occurrence of the extraordinary event.
In such a scenario, the agency may not
have complete data to submit to CMS.
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We believe that it may be appropriate,
in these situations, to grant a full
exception to the reporting requirements
for a specific period of time.
We do not wish to penalize HHAs in
these circumstances or to unduly
increase their burden during these
times. Therefore, we proposed a process
for HHAs to request and for us to grant
exceptions and extensions for the
reporting requirements of the HH QRP
for one or more quarters, beginning with
the CY 2019 HH QRP, when there are
certain extraordinary circumstances
outside the control of the HHA. When
an exception or extension is granted, we
would not reduce the HHA’s PPS
payment for failure to comply with the
requirements of the HH QRP.
We proposed that if an HHA seeks to
request an exception or extension for
the HH QRP, the HHA must request an
exception or extension within 90 days
of the date that the extraordinary
circumstances occurred. The HHA may
request an exception or extension for
one or more quarters by submitting a
written request to CMS that contains the
information noted below, via email to
the HHA Exception and Extension
mailbox at HHAPureConsiderations@
cms.hhs.gov. Requests sent to CMS
through any other channel would not be
considered as valid requests for an
exception or extension from the HH
QRP’s reporting requirements for any
payment determination.
The subject of the email must read
‘‘HH QRP Exception or Extension
Request’’ and the email must contain
the all following information:
• HHA CCN.
• HHA name.
• CEO or CEO-designated personnel
contact information including name,
telephone number, email address, and
mailing address (the address must be a
physical address, not a post office box).
• HHA’s reason for requesting an
exception or extension.
• Evidence of the impact of
extraordinary circumstances, including
but not limited to photographs,
newspaper and other media articles.
• A date when the HHA believes it
will be able to again submit HH QRP
data and a justification for the proposed
date.
We proposed that exception and
extension requests would need to be
signed by the HHA’s CEO or CEOdesignated personnel, and that if the
CEO designates an individual to sign the
request, the CEO-designated individual
would be able to submit such a request
on behalf of the HHA. Following receipt
of the email, we would provide a: (1)
Written acknowledgement, using the
contact information provided in the
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email, to the CEO or CEO-designated
contact notifying them that the request
has been received; and (2) a formal
response to the CEO or any CEOdesignated HHA personnel, using the
contact information provided in the
email, indicating our decision.
We stated that this proposal would
not preclude us from granting
exceptions or extensions to HHAs that
have not requested them when we
determine that an extraordinary
circumstance, such as an act of nature,
affects an entire region or locale. If we
were to make the determination to grant
an exception or extension to all HHAs
in a region or locale, we proposed to
communicate this decision through
routine communication channels to
HHAs and vendors, including, but not
limited to, issuing memos, emails, and
notices on our HH QRP Web site once
it is available at https://www.cms.gov/
Medicare/Quality-Initiatives-PatientAssessment-Instruments/
HomeHealthQualityInits/
HomeHealthQualityReportingReconsideration-and-Exception-andExtension.html.
We also proposed that we may grant
an exception or extension to HHAs if we
determine that a systemic problem with
one of our data collection systems
directly affected the ability of the HHA
to submit data. Because we do not
anticipate that these types of systemic
errors will happen often, we do not
anticipate granting an exception or
extension on this basis frequently.
If an HHA is granted an exception, we
would not require that the HHA submit
any measure data for the period of time
specified in the exception request
decision. If we grant an extension to the
original submission deadline, the HHA
would still remain responsible for
submitting quality data collected during
the timeframe in question, although we
would specify a revised deadline by
which the HHA must submit this
quality data.
We also proposed that any exception
or extension requests submitted for
purposes of the HH QRP would apply to
that program only, and not to any other
program we administer for HHAs such
as survey and certification. OASIS
requirements, including electronic
submission, during Declared Public
Health Emergencies can be found at
FAQs I–5, I–6, I–7, I–8 at https://
www.cms.gov/Medicare/ProviderEnrollment-and-Certification/
SurveyCertEmergPrep/downloads/
AllHazardsFAQs.pdf.
We intend to provide additional
information pertaining to exceptions
and extensions for the HH QRP,
including any additional guidance, on
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the HH QRP Web site at https://
www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HomeHealthQualityReportingReconsideration-and-Exception-andExtension.html.
In the CY 2018 HH PPS proposed rule
(82 FR 35374), we proposed to codify
the HH QRP Submission Exception and
Extension Requirements at § 484.250(d)
of our regulations.
Comment: One commenter expressed
support for the creation of an exception
and extension request process for HHAs
that experience disasters or other
extraordinary circumstances.
Response: We thank the commenter
for the comment and support.
Final Decision: After consideration of
comments received, we are finalizing
the adoption of the policy as proposed
for HH QRP Submission Exception and
Extension Requirements beginning with
the CY 2019 HH QRP and our decision
to codify the HH QRP Submission
Exception and Extension Requirements
at § 484.250(d) of our regulations.
3. HH QRP Submission Reconsideration
and Appeals Procedures
The HH QRP reconsiderations and
appeals process was finalized in the CY
2013 HH PPS final rule (77 FR 67096).
At the conclusion of the required
quality data reporting and submission
period, we review the data received
from each HHA during that reporting
period to determine if the HHA met the
HH QRP reporting requirements. HHAs
that are found to be noncompliant with
the HH QRP reporting requirements for
the applicable calendar year will receive
a 2 percentage point reduction to its
market basket percentage update for that
calendar year.
Similar to our other quality reporting
programs, such as the SNF QRP, the
LTCH QRP, and the IRF QRP, we
include an opportunity for the providers
to request a reconsideration of our
initial noncompliance determination.
To be consistent with other established
quality reporting programs and to
provide an opportunity for HHAs to
seek reconsideration of our initial
noncompliance decision, in the CY 2018
HH PPS proposed rule (82 FR 35374
through 35375) we proposed a process
that enables an HHA to request
reconsideration of our initial noncompliance decision in the event that it
believes that it was incorrectly
identified as being non-compliant with
the HH QRP reporting requirements for
a particular calendar year.
For the CY 2019 HH QRP, and
subsequent years, we proposed a HHA
would receive a notification of
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noncompliance if we determine that the
HHA did not submit data in accordance
with the HH QRP reporting
requirements for the applicable CY. The
purpose of this notification is to put the
HHA on notice that the HHA: (1) Has
been identified as being non-compliant
with the HH QRP’s reporting
requirements for the applicable calendar
year; (2) will be scheduled to receive a
reduction in the amount of two
percentage points to its market basket
percentage update for the applicable
calendar year; (3) may file a request for
reconsideration if it believes that the
finding of noncompliance is erroneous,
has submitted a request for an extension
or exception that has not yet been
decided, or has been granted an
extension or exception; and (4) must
follow a defined process on how to file
a request for reconsideration, which will
be described in the notification.
We stated that we would only
consider requests for reconsideration
after an HHA has been found to be
noncompliant.
Notifications of noncompliance and
any subsequent notifications from CMS
would be sent via a traceable delivery
method, such as certified U.S. mail or
registered U.S. mail, or through other
practicable notification processes, such
as a report from CMS to the provider as
a Certification and Survey Provider
Enhanced Reports (CASPER) report, that
will provide information pertaining to
their compliance with the reporting
requirements for the given reporting
cycle or from the Medicare
Administrative Contractors assigned to
process the provider’s claims. To obtain
the compliance reports, we stated that
HHAs must access the CASPER
Reporting Application. HHAs can access
the CASPER Reporting application via
their CMS OASIS System Welcome page
by selecting the CASPER Reporting link.
The ‘‘CASPER Reports’’ link will
connect an HHA to the QIES National
System Login page for CASPER
Reporting.
We proposed to disseminate
communications regarding the
availability of compliance reports
through routine channels to HHAs and
vendors, including, but not limited to
issuing memos, emails, Medicare
Learning Network (MLN)
announcements, and notices on our HH
QRP Web site once it is available at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HomeHealthQualityReportingReconsideration-and-Exception-andExtension.html.
We proposed that an HHA would
have 30 days from the date of the letter
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51739
of noncompliance to submit to us a
request for reconsideration. This
proposed time frame would allow us to
balance our desire to ensure that HHA
s have the opportunity to request
reconsideration with our need to
complete the process and provide HHAs
with our reconsideration decision in a
timely manner. We proposed that an
HHA may withdraw its request at any
time and may file an updated request
within the proposed 30-day deadline.
We also proposed that, in very limited
circumstances, we may grant a request
by an HHA to extend the proposed
deadline for reconsideration requests.
We stated that it would be the
responsibility of an HHA to request an
extension and demonstrate that
extenuating circumstances existed that
prevented the filing of the
reconsideration request by the proposed
deadline.
We also proposed that as part of the
HHA’s request for reconsideration, the
HHA would be required to submit all
supporting documentation and evidence
demonstrating full compliance with all
HH QRP reporting requirements for the
applicable calendar year, that the HHA
has requested an extension or exception
for which a decision has not yet been
made, that the HHA has been granted an
extension or exception, or has
experienced an extenuating
circumstance as defined in section V.I.2.
of this final rule, but failed to file a
timely request of exception. We
proposed that we would not review any
reconsideration request that fails to
provide the necessary documentation
and evidence along with the request.
We proposed that the documentation
and evidence may include copies of any
communications that demonstrate the
HHA’s compliance with the HH QRP, as
well as any other records that support
the HHA’s rationale for seeking
reconsideration, but must not include
any protected health information (PHI).
We stated that we intended to provide
a sample list of acceptable supporting
documentation and evidence, as well as
instructions for HHAs on how to
retrieve copies of the data submitted to
CMS for the appropriate program year in
the future on our HH QRP Web site at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HomeHealthQualityReportingReconsideration-and-Exception-andExtension.html.
We proposed that an HHA wishing to
request a reconsideration of our initial
noncompliance determination would be
required to do so by submitting an email
to the following email address:
HHAPureConsiderations@cms.hhs.gov.
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Any request for reconsideration
submitted to us by an HHA would be
required to follow the guidelines
outlined on our HH QRP Web site once
it is available once it is available at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HomeHealthQualityReportingReconsideration-and-Exception-andExtension.html.
All emails must contain a subject line
that reads ‘‘HH QRP Reconsideration
Request.’’ Electronic email submission
is the only form of reconsideration
request submission that will be accepted
by us. We proposed that any
reconsideration requests communicated
through another channel including, but
not limited to, U.S. Postal Service or
phone, would not be considered as a
valid reconsideration request.
We proposed that a reconsideration
request include the all of the following
information:
• HHA CMS Certification Number
(CCN).
• HHA Business Name.
• HHA Business Address.
• The CEO contact information
including name, email address,
telephone number, and physical mailing
address; or the CEO-designated
representative contact information
including name, title, email address,
telephone number and physical mailing
address.
• CMS identified reason(s) for
noncompliance from the noncompliance notification.
• The reason(s) for requesting
reconsideration.
We proposed that the request for
reconsideration must be accompanied
by supporting documentation
demonstrating compliance. Following
receipt of a request for reconsideration,
we would provide an email
acknowledgment, using the contact
information provided in the
reconsideration request, to the CEO or
CEO-designated representative that the
request has been received. Once we
have reached a decision regarding the
reconsideration request, an email would
be sent to the HHA CEO or CEO
designated representative, using the
contact information provided in the
reconsideration request, notifying the
HHA of our decision.
We also proposed that the
notifications of our decision regarding
reconsideration requests may be made
available through a traceable delivery
method, such as certified U.S. mail or
registered U.S. mail or through the use
of CASPER reports. If the HHA is
dissatisfied with the decision rendered
at the reconsideration level, the HHA
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may appeal the decision to the PRRB
under 42 CFR 405.1835. We believe the
proposed process is more efficient and
less costly for CMS and for HHAs
because it decreases the number of
PRRB appeals by resolving issues earlier
in the process. Additional information
about the reconsideration process
including details for submitting a
reconsideration request will be posted
in the future to our HH QRP Web site
at https://www.cms.gov/Medicare/
Quality-Initiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
HomeHealthQualityReportingReconsideration-and-Exception-andExtension.html.
In the CY 2018 HH PPS proposed rule
(82 FR 35375), we proposed to add the
HH QRP Submission Reconsideration
and Appeals Procedures at §§ 484.250(e)
and (f) of our regulations.
Comment: One commenter expressed
support for the submission
reconsideration and appeals procedures
for HHAs.
Response: We thank the commenter
for the comment and support.
Final Decision: After consideration of
the public comments received, we are
finalizing as proposed the adoption of
the policy for HH QRP Submission
Reconsideration and Appeals
Procedures for the CY 2019 HH QRP
and subsequent years, which will be
codified at § 484.250(e) and (f) of our
regulations.
K. Policies Regarding Public Display of
Quality Measure Data for the HH QRP
Our home health regulations, at
§ 484.250(a), require HHAs to submit
OASIS assessments and Home Health
Care Consumer Assessment of
Healthcare Providers and Systems
Survey® (HHCAHPS) data to meet the
quality reporting requirements of
section 1895(b)(3)(B)(v) of the Act.
Section 1899B(g) of the Act requires that
data and information of provider
performance on quality measures and
resource use and other measures be
made publicly available beginning not
later than 2 years after the applicable
specified ‘‘application date’’. In
addition, section 1895(b)(3)(B)(v)(III) of
the Act requires the Secretary to
establish procedures for making data
submitted under section
1895(b)(3)(B)(v)(II) of the Act available
to the public, and section 1899B(g)(1) of
the Act requires the Secretary to do the
same with respect to HHA performance
on measures specified under sections
1899B(c)(1) and (d)(1) of the Act.
Section 1895(b)(3)(B)(v)(III) of the Act
requires that the public reporting
procedures for data submitted under
subclause (II) ensure that a HHA has the
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opportunity to review the data that is to
be made public with respect to it prior
to such data being made public. Under
section 1899B(g)(2) of the Act, the
public reporting procedures for
performance on measures under
sections 1899B(c)(1) and (d)(1) of the
Act must ensure, including through a
process consistent with the process
applied under section
1886(b)(3)(B)(viii)(VII) of the Act,
(which refers to public display and
review requirements in the Hospital
Inpatient Quality Reporting (Hospital
IQR) Program), that a HHA has the
opportunity to review and submit
corrections to its data and information
that are to be made public for the agency
prior to such data being made public.
We recognize that public reporting of
quality data is a vital component of a
robust quality reporting program and are
fully committed to ensuring that the
data made available to the public are
meaningful. Further, we agree that
measures for comparing performance
across home health agencies must be
constructed from data collected in a
standardized and uniform manner.
In the CY 2017 HH PPS final rule (81
FR 76785 through 76786), we finalized
procedures that allow individual HHAs
to review and correct their data and
information on IMPACT Act measures
that are to be made public before those
measure data are made public.
Information on how to review and
correct data on IMPACT Act measures
that are to be made public before those
measure data are made public can be
found on the HH QRP Web site at
https://www.cms.gov/Medicare/QualityInitiatives-Patient-AssessmentInstruments/HomeHealthQualityInits/
Home-Health-Quality-ReportingRequirements.html. We did not propose
any changes to these policies in the CY
2018 HH PPS proposed rule.
However, in the CY 2018 HH PPS
proposed rule (82 FR 35375 and 35376),
pending the availability of data, we
proposed to publicly report data
beginning in CY 2019 for the following
two assessment-based measures: (1)
Percent of Patients or Residents with
Pressure Ulcers that are New or
Worsened (NQF #0678); and (2) Drug
Regimen Review Conducted with
Follow-Up for Identified Issues—PAC
HH QRP. Data collection for these two
assessment-based measures began on
OASIS on January 1, 2017. We proposed
to publicly report data beginning in CY
2019 for these assessment-based
measures based on four rolling quarters
of data, beginning with data collected
for discharges in 2017.
We proposed to publicly report data
beginning in CY 2019 for the following
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3 claims-based measures: (1) Medicare
Spending Per Beneficiary—PAC HH
QRP; (2) Discharge to Community-PAC
HH QRP; and (3) Potentially Preventable
30-Day Post-Discharge Readmission
Measure for HH QRP. As adopted in the
CY 2017 HH PPS final rule (81 FR
43773), for the MSPB–PAC HH QRP
measure, we will use 1 year of claims
data beginning with CY 2016 claims
data to inform confidential feedback
reports for HHAs, and CY 2017 claims
data for public reporting for the HH
QRP. For the Discharge to Community—
PAC HH QRP measure we will use 2
years of claims data, beginning with CYs
2015 and 2016 claims data to inform
confidential feedback and CYs 2016 and
2017 claims data for public reporting.
For the Potentially Preventable 30-Day
Post-Discharge Readmission Measure for
HH QRP, we will use 3 years of claims
data, beginning with CY 2014, 2015 and
2016 claims data to inform confidential
feedback reports for HHAs, and CY
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2015, 2016 and 2017 claims data for
public reporting.
Finally, we proposed to assign HHAs
with fewer than 20 eligible cases during
a performance period to a separate
category: ‘‘The number of patient
episodes for this measure is too small to
report,’’ 102 to ensure the statistical
reliability of the measures. If a HHA had
fewer than 20 eligible cases, the HHA’s
performance would not be publicly
reported for the measure for that
performance period.
TABLE 22—NEW HH QRP MEASURES PROPOSED FOR CY 2019 PUBLIC DISPLAY
asabaliauskas on DSKBBXCHB2PROD with RULES
Proposed measures:
Percent of Residents or Patients with Pressure Ulcers that Are New or Worsened (Short Stay) (NQF #0678).
Drug Regimen Review Conducted with Follow-Up for Identified Issues—PAC HH QRP.
Potentially Preventable 30-Day Post-Discharge Readmission Measure for HH QRP.
Discharge to Community—(PAC) HH QRP.
Medicare Spending Per Beneficiary (PAC) HH QRP.
We invited public comments on these
proposals for the public display of
quality data.
Comment: Commenters provide
feedback regarding the public display of
quality measures beginning CY 2019 for
data collected beginning CY 2017. One
commenter questioned if the Medicare
Spending Per Beneficiary—PAC HH
QRP measure includes spending data
that is specific to HH services or the
total amount of Medicare spending for
beneficiaries specific to a defined
timeframe. One commenter did not
support public reporting for the
Discharge to Community—PAC HH QRP
measure based on the potential for
providers to have incentives against the
appropriate use of hospice services in a
patient-centered continuum of care.
Another commenter did not support
publicly reporting the Drug Regimen
Review Conducted with Follow-Up for
Identified Issues—PAC HH QRP
measure, stating that this measure is
dependent on physician response and is
not a measure of HHA quality or
performance. Finally, a commenter
suggested a dashboard of measures
aligned across home health quality
initiatives, including star ratings, Home
Health Compare and the HH VBP
demonstration.
Response: We appreciate the
commenters’ suggestions regarding the
public display of quality measures. As
finalized in the CY 2017 rule, the
MSPB–PAC HH QRP measure episode is
comprised of a treatment period and an
associated services period. The
treatment period includes those services
that are provided directly by the HHA.
The associated services period is the
time during which Medicare Part A and
Part B services that are not treatment
services are counted towards the
episode, subject to certain exclusions,
such as planned admissions and organ
transplants. More detailed specifications
for the MSPB–PAC measures, including
the MSPB–PAC HH QRP measure, are
available at https://www.cms.gov/
Medicare/Quality-Initiatives-PatientAssessment-Instruments/
HomeHealthQualityInits/
HHQIQualityMeasures.html.
The Discharge to Community measure
excludes patients discharged to home or
facility-based hospice care. Thus,
discharges to hospice are not considered
discharges to community, but rather are
excluded from the measure calculation.
We wish to also note that including 31day post-discharge mortality outcomes
is intended to identify successful
discharges to community, and to avoid
the potential unintended consequence
of inappropriate community discharges
that bypass hospice care. With respect
to the public reporting of Drug Regimen
Review Conducted with Follow-Up for
Identified Issues, the intent of the
measure is to capture timely follow up
for all potential clinically significant
issues. We believe the timely review
and follow up of potentially clinically
significant medication issues at every
assessment time period and across the
patient’s episode of care is essential for
providing the best quality care for
patients, and that this measure helps to
ensure that high quality care services
are furnished and that patient harm is
avoided.
102 This language is currently available as
Footnote #4 on Home Health Compare (https://
With regard to the commenter’s
suggestion that we provide a dashboard
that communicates alignment across the
measures, we will take the commenter’s
suggestion under consideration.
Comment: We received several
comments about the Quality of Patient
Care star ratings. One commenter noted
increased administrative and clinical
costs HHAs incur to maintain or
improve the number of stars instead of
focusing on improving the scores on
individual quality measures. Another
commenter stated that poor performing
home health agencies could rate higher
than their actual performance while
good or excellent agencies could rate
lower than their actual performance due
to the way the data is calculated.
Response: We thank the commenters,
but note that these comments relate to
issues for which we made no proposals
in the CY 2018 HH proposed rule.
Therefore, we believe these comments
to be outside the scope of the proposed
rule and will not address them here.
Final Decision: After considering the
comments received, we are finalizing
our proposals regarding public display
of quality measure data in the HH QRP.
www.medicare.gov/HomeHealthCompare/Data/
Footnotes.html).
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L. Mechanism for Providing Confidential
Feedback Reports to HHAs
Section 1899B(f) of the Act requires
the Secretary to provide confidential
feedback reports to post-acute care
(PAC) providers on their performance
on the measures specified under
subsections (c)(1) and (d)(1) of section
1899B of the Act, beginning one year
after the specified application date that
applies to such measures and PAC
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providers. In the CY 2017 HH PPS final
rule (81 FR 76702), we finalized
processes to allow HH providers the
opportunity to review their data and
information using confidential feedback
reports that will enable HHAs to review
their performance on the measures
required under the HH QRP.
Information on how to obtain these and
other reports available to the HH QRP
can be found at https://www.cms.gov/
Medicare/Quality-Initiatives-PatientAssessment-Instruments/
HomeHealthQualityInits/Home-HealthQuality-Reporting-Requirements.html.
We did not propose any changes to this
policy.
asabaliauskas on DSKBBXCHB2PROD with RULES
M. Home Health Care CAHPS® Survey
(HHCAHPS)
In the CY 2017 HH PPS final rule (81
FR 76787), we stated that the home
health quality measures reporting
requirements for Medicare-certified
agencies includes the Home Health Care
CAHPS® (HHCAHPS) Survey for the
Home Health Quality Reporting Program
and along with OASIS measures,
HHCAHPS participation is required for
the Annual Payment Update (APU). In
the CY 2017 HH PPS final rule, we
finalized the reporting requirements and
the data submission dates for the CY
2017–CY 2020 APU periods. We
proposed to continue the HHCAHPS
requirements in future years for the
continuous monthly data collection and
quarterly data submission of HHCAHPS
data.
1. Background and Description of
HHCAHPS
The HHCAHPS survey is part of a
family of CAHPS® surveys that asks
patients to report on and rate their
experiences with health care. For more
details about the HHCAHPS Survey
please see 81 FR 76787 through 76788.
We stated in previous rules that
Medicare-certified HHAs are required to
contract with an approved HHCAHPS
survey vendor. This requirement
continues, and Medicare-certified
agencies are required to provide a
monthly list of their HHCAHPS-eligible
patients to their respective HHCAHPS
survey vendors. Home health agencies
are not allowed to influence their
patients about how the HHCAHPS
survey.
As previously required, new
HHCAHPS survey vendors are required
to attend Introduction training, and
current HHCAHPS vendors are required
to attend Update training conducted by
CMS and the HHCAHPS Survey
Coordination Team. New HHCAHPS
vendors need to pass a post-training
certification test. We have
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approximately 25 approved HHCAHPS
survey vendors. The list of approved
HHCAHPS survey vendors is available
at https://homehealthcahps.org.
2. HHCAHPS Oversight Activities
We stated in prior final rules that all
approved HHCAHPS survey vendors are
required to participate in HHCAHPS
oversight activities to ensure
compliance with HHCAHPS protocols,
guidelines, and survey requirements.
The purpose of the oversight activities
is to ensure that approved HHCAHPS
survey vendors follow the HHCAHPS
Protocols and Guidelines Manual.
In the CY 2013 HH PPS final rule (77
FR 67095 through 67097, 67164), we
codified at § 484.250(c)(3) that all
approved HHCAHPS survey vendors are
required to fully comply with all
HHCAHPS oversight activities.
In the CY 2018 HH PPS proposed rule
(82 FR 35377), we restated the
HHCAHPS requirements for CY 2019,
because participation occurs in the
period of the publication of the
proposed and final rules for CY 2018.
We additionally presented the
HHCAHPS requirements for CY 2020 for
the sake of continuity. We proposed the
HHCAHPS requirements for the CY
2021 Annual Payment Update.
3. HHCAHPS Requirements for the CY
2019 HH QRP
In the CY 2017 HH PPS final rule (81
FR 76789), we finalized the
requirements for the CY 2019 HH QRP.
For the CY 2019 HH QRP, we require
continuous monthly HHCAHPS data
collection and reporting for four
quarters. The data collection period for
the CY 2018 HH QRP includes the
second quarter 2017 through the first
quarter 2018 (the months of April 2017
through March 2018). HHAs will be
required to submit their HHCAHPS data
files to the HHCAHPS Data Center for
the second quarter 2017 by 11:59 p.m.,
eastern daylight time (e.d.t.) on October
19, 2017; for the third quarter 2017 by
11:59 p.m., eastern standard time (e.s.t.)
on January 18, 2018; for the fourth
quarter 2017 by 11:59 p.m., e.d.t. on
April 19, 2018; and for the first quarter
2018 by 11:59 p.m., e.d.t. on July 19,
2018. These deadlines are firm; no
exceptions will be permitted.
For more details on the CY 2019 HH
QRP, we refer readers to 81 FR 76789.
4. HHCAHPS Requirements for the CY
2020 HH QRP
In the CY 2017 HH PPS final rule (81
FR 76789), we finalized the
requirements for the CY 2020 HH QRP.
For the CY 2020 HH QRP, we require
continued monthly HHCAHPS data
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collection and reporting for four
quarters. The data collection period for
the CY 2020 HH QRP includes the
second quarter 2018 through the first
quarter 2019 (the months of April 2018
through March 2019). HHAs will be
required to submit their HHCAHPS data
files to the HHCAHPS Data Center for
the second quarter 2018 by 11:59 p.m.,
e.d.t. on October 18, 2018; for the third
quarter 2018 by 11:59 p.m., e.s.t. on
January 17, 2019; for the fourth quarter
2018 by 11:59 p.m., e.d.t. on April 18,
2019; and for the first quarter 2019 by
11:59 p.m., e.d.t. on July 18, 2019. These
deadlines are firm; no exceptions will
be permitted.
For more details about the CY 2020
HH QRP, we refer readers to 81 FR
76789.
5. HHCAHPS Requirements for the CY
2021 HH QRP
For the CY 2021 HH QRP, we
proposed to require the continued
monthly HHCAHPS data collection and
reporting for four quarters. The data
collection period for the CY 2021 HH
QRP includes the second quarter 2019
through the first quarter 2020 (the
months of April 2019 through March
2020). HHAs will be required to submit
their HHCAHPS data files to the
HHCAHPS Data Center for the second
quarter 2019 by 11:59 p.m., e.d.t. on
October 17, 2019; for the third quarter
2019 by 11:59 p.m., e.s.t. on January 16,
2020; for the fourth quarter 2019 by
11:59 p.m., e.d.t. on April 16, 2020; and
for the first quarter 2020 by 11:59 p.m.,
e.d.t. on July 16, 2020. These deadlines
are firm; no exceptions will be
permitted.
For the CY 2021 HH QRP, we
proposed to require that all HHAs with
fewer than 60 HHCAHPS-eligible
unduplicated or unique patients in the
period of April 1, 2018 through March
31, 2019 are exempt from the HHCAHPS
data collection and submission
requirements for the CY 2021 HH QRP,
upon completion of the CY 2021
HHCAHPS Participation Exemption
Request form, and upon CMS
verification of the HHA patient counts.
Agencies with fewer than 60
HHCAHPS-eligible, unduplicated or
unique patients in the period of April 1,
2018 through March 31, 2019 were
proposed to be required to submit their
patient counts on the CY 2021
HHCAHPS Participation Exemption
Request form posted on https://
homehealthcahps.org from April 1,
2019 to 11:59 p.m., e.d.t. to March 31,
2020. This deadline is firm, as are all of
the quarterly data submission deadlines
for the HHAs that participate in
HHCAHPS.
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We proposed to automatically exempt
HHAs receiving Medicare certification
on or after the start of the period in
which HHAs do their patient count for
a particular year’s HHCAHPS data
submission from the HHCAHPS
reporting requirement for the year. We
proposed that HHAs receiving
Medicare-certification on or after April
1, 2019 would be exempt from the
HHCAHPS reporting requirement for the
CY 2021 HH QRP. As we have finalized
in previous years, we proposed that
these newly-certified HHAs do not need
to complete the HHCAHPS Participation
Exemption Request Form for the CY
2021 HH QRP.
6. HHCAHPS Reconsiderations and
Appeals Process
As finalized in previous rules, we
proposed that HHAs must monitor their
respective HHCAHPS survey vendors to
ensure that vendors submit their
HHCAHPS data on time, by accessing
their HHCAHPS Data Submission
Reports on https://
homehealthcahps.org. This helps HHAs
ensure that their data are submitted in
the proper format for data processing to
the HHCAHPS Data Center.
We proposed to continue HHCAHPS
oversight activities as finalized in the
previous rules. In the CY 2013 HH PPS
final rule (77 FR 67068, 67164), we
codified the current guideline that all
approved HHCAHPS survey vendors
must fully comply with all HHCAHPS
oversight activities. We included this
survey requirement at § 484.250(c)(3).
For further information on the HH
QRP reconsiderations and appeals
process, please see section V.J.3. of this
final rule.
7. Summary
We did not propose any changes to
the participation requirements, or to the
requirements pertaining to the
implementation of the Home Health
CAHPS® Survey (HHCAHPS). We only
proposed updates to the information to
reflect the dates for future HH QRP
years. We encouraged HHAs to keep upto-date about the HHCAHPS by
regularly viewing the official Web site
for the HHCAHPS at https://
homehealthcahps.org. We noted that
HHAs can also send an email to the
HHCAHPS Survey Coordination Team
at hhcahps@rti.org or to CMS at
homehealthcahps@cms.hhs.gov, or
telephone toll-free
(1–866–354–0985) for more information
about the HHCAHPS Survey.
Final Decision: We did not receive
any comments on our proposals.
Accordingly, we are finalizing the
proposals. We again strongly encourage
HHAs to keep up-to-date about the
HHCAHPS by regularly viewing the
official Web site for the HHCAHPS at
https://homehealthcahps.org. HHAs can
also send an email to the HHCAHPS
Survey Coordination Team at hhcahps@
rti.org or to CMS at homehealthcahps@
cms.hhs.gov, or telephone toll-free (1–
866–354–0985) for more information
about the HHCAHPS Survey.
VI. Collection of Information
Requirements
A. Statutory Requirement for
Solicitation of Comments
Under the Paperwork Reduction Act
of 1995 (PRA), we are required to
provide 60-day notice in the Federal
Register and solicit public comment
before a collection of information
requirement is submitted to the OMB for
review and approval. We note that we
51743
will submit a revised information
collection request (OMB control number
0938–1279) to OMB for review. This
will also extend the information
collection request which expires
December 30, 2019. 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.
This final rule makes reference to
associated information collections that
are not discussed in the regulation text
contained in this document.
B. Collection of Information
Requirements for the HH QRP
We believe that the burden associated
with the HH QRP is the time and effort
associated with data collection and
reporting. As of April 1, 2017, there are
approximately 12,149 HHAs reporting
quality data to CMS. For the purposes
of calculating the costs associated with
the collection of information
requirements, we obtained mean hourly
wages for these staff from the U.S.
Bureau of Labor Statistics’ May 2016
National Occupational Employment and
Wage Estimates (https://www.bls.gov/
oes/current/oes_nat.htm). To account
for overhead and fringe benefits (100
percent), we have doubled the hourly
wage. These amounts are detailed in
Table 23.
TABLE 23—U.S. BUREAU OF LABOR STATISTICS’ MAY 2016 NATIONAL OCCUPATIONAL EMPLOYMENT AND WAGE
ESTIMATES
Occupation
code
Occupation title
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Registered Nurse (RN) ....................................................................................
Physical therapists HHAs ................................................................................
Speech-Language Pathologists (SLP) ............................................................
Occupational Therapists (OT) .........................................................................
The OASIS changes that we are
finalizing in section V.D of this final
rule will result in the removal of 70 data
elements from the OASIS at the time
point of Start of Care (SOC), 70 data
elements at the time point of
Resumption of Care (ROC), 18 data
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29–1141
29–1123
29–1127
29–1122
elements at the time point of Follow-up
(FU), 42 data elements at the time point
of Transfer to an Inpatient Facility
(TOC), 1 data element at the time point
of Death at Home (Death), and 34 data
elements at the time point of Discharge
from Agency (Discharge). These data
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Mean hourly
wage
($/hr)
$34.70
46.42
37.60
40.25
Fringe
benefit
(100%)
($/hr)
$34.70
46.42
37.60
40.25
Adjusted
hourly
wage
($/hr)
$69.40
92.84
75.20
80.50
items will not be used in the calculation
of quality measures adopted in the HH
QRP, or for other purposes that are not
related to the HH QRP.
Section V.F.1. of this final rule adopts
a new pressure ulcer measure to replace
the current pressure ulcer measure that
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we previously specified under section
1899B(c)(1)(B) of the Act, beginning
with the CY 2020 HH QRP. The
replacement measure is entitled,
‘‘Changes in Skin Integrity Post-Acute
Care: Pressure Ulcer/Injury.’’ The new
measure will be calculated using data
elements that are currently collected
and reported using the OASIS–C2
(version effective January 1, 2017).
Adoption of the Changes in Skin
Integrity Post-Acute Care: Pressure
Ulcer/Injury measure will result in the
removal of item M1313, which has 6
data elements that cover the same issues
that are addressed in the pressure ulcer
assessment that will be required under
the new pressure ulcer measure, making
it duplicative and no longer necessary to
separately collect.
In sections V.F.2. of this final rule, we
are adopting a new quality measure
under section 1899B(c)(1)(A) of the Act
beginning with the CY 2020 HH QRP
entitled ‘‘Application of Percent of
Long-Term Care Hospital Patients with
an Admission and Discharge Functional
Assessment and a Care Plan That
Addresses Function (NQF #2631).’’ In
the CY 2018 HH PPS proposed rule (82
FR 35379), we stated that if we finalized
the adoption of this measure, we would
add 13 standardized patient assessment
data elements at SOC, 13 data elements
at ROC, 15 standardized patient
assessment data elements at FU, and 13
standardized patient assessment data
elements at Discharge. We inadvertently
did not include in our original burden
estimate two OASIS items (GG0170Q
and GG0170RR) that are needed to
calculate this measure.103 We have
updated our burden estimate to include
these items, and note that as a result of
finalizing this measure, we will be
adding 15 standardized patient
assessment data elements at SOC, 15
standardized patient assessment data
elements at ROC, 16 standardized
patient assessment data elements at FU,
and 15 standardized patient assessment
data elements at Discharge.
In sections V.F.3. of this final rule, we
are adopting a new quality measure
under section 1899B(c)(1)(D) of the Act
beginning with the CY 2020 HH QRP
entitled ‘‘Application of Percent of
Residents Experiencing One or More
Falls with Major Injury (NQF# 0674).’’
The new measure will be calculated
using new standardized data elements
added to the OASIS. Specifically, we are
adding 4 data elements at TOC, 4 data
elements at Death, and 4 data elements
at Discharge.
In sections V.H.2 and V.H.3 of this
final rule, we are finalizing our proposal
to collect standardized patient
assessment data with respect to the
Medical Condition and Comorbidity
category beginning with the CY 2019
HH QRP and Functional Status
beginning with the CY 2020 HH QRP.
As a result, we are adding to the OASIS
the standardized patient assessment
data elements associated with these
categories, which include 17
standardized patient assessment data
elements at SOC, 17 standardized
patient assessment data elements at
ROC, and 12 standardized patient
assessment data elements at Discharge.
We are not finalizing our proposals to
require HHAs to report standardized
patient assessment data elements for
three of the five categories under section
1899B(b)(1)(B) of the Act: Cognitive
Function and Mental Status; Special
Services, Treatments, and Interventions;
and Impairments. As a result, we will
not be adding to the OASIS the data
elements associated with these
proposals, which included 36 data
elements at SOC, 36 data elements at
ROC, or 24 data elements at discharge.
The OASIS instrument is used for
both the HH QRP and the HH PPS. In
sections III.E. of this final rule, after
receiving detailed comments from the
public we are not finalizing the
implementation of the HHGM.
Therefore, we are not finalizing the
proposal to add two current OASIS–C2
items, M1033 and M1800, at the FU
time point or to remove collection of
eight current OASIS–C2 integumentary
status items at the FU time point.
In summary, as a net result of the
policies we are finalizing in this final
rule, we will be removing 38 data
elements at SOC, 38 data elements at
ROC, 2 data elements at FU, 38 data
elements at TOC and 9 data elements at
Discharge. We will be adding 3 data
elements at Death.
Under section 1899B(m) of the Act,
the Paperwork Reduction Act does not
apply to section 1899B, or to the
sections of the OASIS that require
modification to achieve the
standardization of patient assessment
data. We are, however, setting out the
burden as a courtesy to advise interested
parties of the actions’ time and costs
and for reference in the regulatory
impact analysis (RIA) section VII. of this
final rule. The requirement and burden
will be submitted to OMB for review
and approval when the modifications to
the OASIS have achieved
standardization and are no longer
exempt from the requirements under
section 1899B(m) of the Act.
We assume that each data element
requires 0.3 minutes of clinician time to
complete. Therefore, there is a reduction
in clinician burden per OASIS
assessment of 11.4 minutes at SOC, 11.4
minutes at ROC, 0.6 minutes at FU, 11.4
minutes at TOC 2.7 minutes at
Discharge. There is an increase in
clinician burden per assessment of 0.9
minutes at Death.
The OASIS is completed by RNs or
PTs, or very occasionally by
occupational therapists (OT) or speech
language pathologists (SLP/ST). Data
from 2016 show that the SOC/ROC
OASIS is completed by RNs
(approximately 87 percent of the time),
PTs (approximately 12.7 percent of the
time), and other therapists, including
OTs and SLP/STs (approximately 0.3
percent of the time). Based on this
analysis, we estimated a weighted
clinician average hourly wage of $72.40,
inclusive of fringe benefits, using the
hourly wage data in Table 23.
Individual providers determine the
staffing resources necessary.
Table 24 shows the total number of
assessments submitted in CY 2016 and
estimated burden at each time point.
TABLE 24—CY 2016 OASIS SUBMISSIONS AND ESTIMATED BURDEN, BY TIME POINT
CY 2016
assessments
completed
asabaliauskas on DSKBBXCHB2PROD with RULES
Time point
Start of Care ................................................................................................................................................
Resumption of Care .....................................................................................................................................
Follow-up .....................................................................................................................................................
Transfer to an inpatient facility ....................................................................................................................
Death at Home ............................................................................................................................................
Discharge from agency ................................................................................................................................
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E:\FR\FM\07NOR2.SGM
6,261,934
1,049,247
3,797,410
1,892,099
41,128
5,120,124
07NOR2
Estimated
burden
($)
¥$86,139,164.10
¥14,443,441.73
¥2,749,324.84
¥26,027,713.84
44,665.01
¥16,681,363.99
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51745
TABLE 24—CY 2016 OASIS SUBMISSIONS AND ESTIMATED BURDEN, BY TIME POINT—Continued
CY 2016
assessments
completed
Time point
Total ......................................................................................................................................................
18,161,942
Estimated
burden
($)
¥145,986,343.50
* Estimated Burden ($) at each Time-Point = (# CY 2016 Assessments Completed) x (clinician burden [min]/60) x ($72.40 [weighted clinician
average hourly wage]).
Based on the data in Table 24, for the
12,149 active Medicare-certified HHAs
in April 2017, we estimate the total
average decrease in cost associated with
changes to the HH QRP at $12,016.33
per HHA annually, or $145,986,343.50
for all HHAs annually. This corresponds
to an estimated reduction in clinician
burden associated with changes to the
HH QRP of 166 hours per HHA
annually, or 2,016,386 hours for all
HHAs annually. This decrease in
burden will be accounted for in the
information collection under OMB
control number 0938–1279.
C. Submission of PRA-Related
Comments
We have submitted a copy of this final
rule to OMB for its review of the rule’s
information collection and
recordkeeping requirements. The
requirements are not effective until they
have been approved by OMB.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.gov/Regulations-andGuidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
See this final rule’s DATES and
ADDRESSES sections for the comment
due date and for additional instructions.
asabaliauskas on DSKBBXCHB2PROD with RULES
VII. Regulatory Impact Analysis
A. Statement of Need
Section 1895(b)(1) of the Act requires
the Secretary to establish a HH PPS for
all costs of home health services paid
under Medicare. In addition, section
1895(b) of the Act requires: (1) The
computation of a standard prospective
payment amount include all costs for
home health services covered and paid
for on a reasonable cost basis and that
such amounts be initially based on the
most recent audited cost report data
available to the Secretary; (2) the
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prospective payment amount under the
HH PPS to be an appropriate unit of
service based on the number, type, and
duration of visits provided within that
unit; and (3) the standardized
prospective payment amount be
adjusted to account for the effects of
case-mix and wage levels among HHAs.
Section 1895(b)(3)(B) of the Act
addresses the annual update to the
standard prospective payment amounts
by the HH applicable percentage
increase. Section 1895(b)(4) of the Act
governs the payment computation.
Sections 1895(b)(4)(A)(i) and
(b)(4)(A)(ii) of the Act require the
standard prospective payment amount
to be adjusted for case-mix and
geographic differences in wage levels.
Section 1895(b)(4)(B) of the Act requires
the establishment of appropriate casemix adjustment factors for significant
variation in costs among different units
of services. Lastly, section 1895(b)(4)(C)
of the Act requires the establishment of
wage adjustment factors that reflect the
relative level of wages, and wage-related
costs applicable to home health services
furnished in a geographic area
compared to the applicable national
average level.
Section 1895(b)(3)(B)(iv) of the Act
provides the Secretary with the
authority to implement adjustments to
the standard prospective payment
amount (or amounts) for subsequent
years to eliminate the effect of changes
in aggregate payments during a previous
year or years that was the result of
changes in the coding or classification
of different units of services that do not
reflect real changes in case-mix. Section
1895(b)(5) of the Act provides the
Secretary with the option to make
changes to the payment amount
otherwise paid in the case of outliers
because of unusual variations in the
type or amount of medically necessary
care. Section 1895(b)(3)(B)(v) of the Act
requires HHAs to submit data for
purposes of measuring health care
quality, and links the quality data
submission to the annual applicable
percentage increase.
The HHVBP Model will apply a
payment adjustment based on an HHA’s
performance on quality measures to test
the effects on quality and expenditures.
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B. Overall Impact
We have examined the impacts of this
final 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), the Regulatory
Flexibility Act (RFA) (September 19,
1980, Pub. L. 96–354), section 1102(b) of
the Act, section 202 of the Unfunded
Mandates Reform Act of 1995 (UMRA,
March 22, 1995; Pub. L. 104–4),
Executive Order 13132 on Federalism
(August 4, 1999), the Congressional
Review Act (5 U.S.C. 804(2) and
Executive Order 13771 on Reducing
Regulation and Controlling Regulatory
Costs (January 30, 2017).
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). We included a detailed
alternatives considered section in the
CY 2018 HH PPS proposed rule, which
outlined alternatives considered for the
CY 2018 HH PPS payment update, the
proposed HHGM, and HH VBP model
(82 FR 35388 and 35389).
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 $100 million or more in any
1 year, or adversely and materially
affecting a sector of the economy,
productivity, competition, jobs, the
environment, public health or safety, or
state, local or tribal governments or
communities (also referred to as
‘‘economically significant’’); (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 novel legal or policy issues
arising out of legal mandates, the
President’s priorities, or the principles
set forth in the Executive Order.
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Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
A regulatory impact analysis (RIA)
must be prepared for major rules with
economically significant effects ($100
million or more in any 1 year). The
savings impacts related to the HHVBP
Model as a whole are estimated at a total
projected 5-year gross savings of $378
million assuming a savings estimate of
a 6 percent annual reduction in
hospitalizations and a 1.0 percent
annual reduction in SNF admissions;
the portion attributable to this final rule
is negligible. In section VII. of this final
rule, we identified a reduction in our
regulatory reporting burden of $
145,986,343.50. We estimate that this
rulemaking is ‘‘economically
significant’’ as measured by the $100
million threshold, and hence also a
major rule under the Congressional
Review Act. Accordingly, we have
prepared a Regulatory Impact Analysis
that, to the best of our ability, presents
the costs and benefits of the rulemaking.
In addition, section 1102(b) of the Act
requires us to prepare a RIA 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 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. This rule
is applicable exclusively to HHAs.
Therefore, the Secretary has determined
this final rule will not have a significant
economic impact on the operations of
small rural hospitals.
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 2017, that
threshold is approximately $148
million. This final rule is not
anticipated to have an effect on State,
local, or tribal governments, in the
aggregate, or on the private sector of
$148 million or more.
If regulations impose administrative
costs on private entities, such as the
time needed to read and interpret this
final rule, we must estimate the cost
associated with regulatory review. Due
to the uncertainty involved with
accurately quantifying the number of
entities that will review the rule, we
assume that the total number of unique
commenters on this year’s proposed rule
will be the number of reviewers of this
final rule. We acknowledge that this
assumption may understate or overstate
the costs of reviewing this final rule. It
is possible that not all commenters
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reviewed this year’s rule in detail, and
it is also possible that some reviewers
chose not to comment on the proposed
rule. For these reasons we believe that
the number of commenters will be a fair
estimate of the number of reviewers of
this final rule.
We also recognize that different types
of entities are in many cases affected by
mutually exclusive sections of this
proposed rule, and therefore for the
purposes of our estimate we assume that
each reviewer reads approximately 50
percent of the rule.
Using the 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 $105.16 per hour, including overhead
and fringe benefits (https://www.bls.gov/
oes/2016/may/naics4_621100.htm).
Assuming an average reading speed, we
estimate that it will take approximately
2.6 hours for the staff to review half of
this final rule. For each HHA that
reviews the rule, the estimated cost is
$273.42 (2.6 hours x $105.16).
Therefore, we estimate that the total cost
of reviewing this regulation is
$368,023.32 ($273.42 x 1,346
reviewers).
1. HH PPS for CY 2018
The update set forth in this final rule
applies to Medicare payments under HH
PPS in CY 2018. Accordingly, the
following analysis describes the impact
in CY 2018 only. We estimate that the
net impact of the policies in this final
rule is approximately $80 million in
decreased payments to HHAs in CY
2018. We applied a wage index budget
neutrality factor and a case-mix weights
budget neutrality factor to the rates as
discussed in section III.C.3. of this final
rule. Therefore, the estimated impact of
the 2018 wage index and the
recalibration of the case-mix weights for
2018 is zero. The ¥$80 million impact
reflects the distributional effects of a 0.5
percent reduction in payments due to
the sunset of the rural add-on provision
($100 million decrease), a 1 percent
home health payment update percentage
($190 million increase), and a ¥0.97
percent adjustment to the national,
standardized 60-day episode payment
rate to account for nominal case-mix
growth for an impact of ¥0.9 percent
($170 million decrease). The $80
million in decreased payments is
reflected in the last column of the first
row in Table 25 as a 0.4 percent
decrease in expenditures when
comparing CY 2017 payments to
estimated CY 2018 payments.
The RFA requires agencies to analyze
options for regulatory relief of small
entities, if a rule has a significant impact
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Fmt 4701
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on a substantial number of small
entities. For purposes of the RFA, small
entities include small businesses,
nonprofit organizations, and small
governmental jurisdictions. Most
hospitals and most other providers and
suppliers are small entities, either by
nonprofit status or by having revenues
of less than $7.5 million to $38.5
million in any one year. For the
purposes of the RFA, we estimate that
almost all HHAs are small entities as
that term is used in the RFA.
Individuals and states are not included
in the definition of a small entity. The
economic impact assessment is based on
estimated Medicare payments
(revenues) and HHS’s practice in
interpreting the RFA is to consider
effects economically ‘‘significant’’ only
if greater than 5 percent of providers
reach a threshold of 3 to 5 percent or
more of total revenue or total costs. The
majority of HHAs’ visits are Medicarepaid visits, and therefore, the majority
of HHAs’ revenue consists of Medicare
payments. Based on our analysis, we
conclude that the policies in this final
rule will result in an estimated total
impact of 3 to 5 percent or more on
Medicare revenue for greater than 5
percent of HHAs. Therefore, the
Secretary has determined that this HH
PPS rule will have a significant
economic impact on a substantial
number of small entities. Further detail
is presented in Table 25, by HHA type
and location.
With regards to options for regulatory
relief, the sunset of rural add-on
payments for CY 2018 is statutory and
we do not have the authority to
authorize rural add-on payments past
December 31, 2017. We believe it is
appropriate to reduce the national,
standardized 60-day episode payment
amount by 0.97 percent in CY 2018 to
account for the estimated increase in
nominal case-mix in order to move
towards more accurate payment for the
delivery of home health services where
payments better align with the costs of
providing such services.
2. HHVBP Model
Under the HHVBP Model, the first
payment adjustment will apply in CY
2018 based on PY1 (2016) data and the
final payment adjustment will apply in
CY 2022 based on PY5 (2020) data. In
the CY 2016 HH PPS final rule, we
estimated that the overall impact of the
HHVBP Model from CY 2018 through
CY 2022 was a reduction of
approximately $380 million (80 FR
68716). In the CY 2017 HH PPS final
rule, we estimated that the overall
impact of the HHVBP Model from CY
2018 through CY 2022 was a reduction
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Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
of approximately $378 million (81 FR
76795). We do not believe the changes
finalized in this final rule will affect the
prior estimates.
C. Detailed Economic Analysis
This final rule updates for CY 2018
the HH PPS rates contained in the CY
2017 HH PPS final rule (81 FR 76702
through 76797). The impact analysis of
this final rule presents the estimated
expenditure effects of policy changes
that are be finalized. We use the latest
data and best analysis available, but we
do not make adjustments for future
changes in such variables as number of
visits or case-mix.
This analysis incorporates the latest
estimates of growth in service use and
payments under the Medicare HH
benefit, based primarily on Medicare
claims data from 2016. We note that
certain events may combine to limit the
scope or accuracy of our impact
analysis, because such an analysis is
future-oriented and, thus, susceptible to
errors resulting from other changes in
the impact time period assessed. Some
examples of such possible events are
newly-legislated general Medicare
program funding changes made by the
Congress, or changes specifically related
to HHAs. In addition, changes to the
Medicare program may continue to be
made as a result of the Affordable Care
Act, or new statutory provisions.
Although these changes may not be
specific to the HH PPS, the nature of the
Medicare program is such that the
changes may interact, and the
complexity of the interaction of these
changes could make it difficult to
predict accurately the full scope of the
impact upon HHAs.
1. HH PPS for CY 2018
Table 25 represents how HHA
revenues are likely to be affected by the
policy changes in this final rule for CY
2018. For this analysis, we used an
analytic file with linked CY 2016 OASIS
assessments and HH claims data for
dates of service that ended on or before
December 31, 2016. The first column of
Table 25 classifies HHAs according to a
number of characteristics including
provider type, geographic region, and
urban and rural locations. The second
column shows the number of facilities
in the impact analysis. The third
column shows the payment effects of
the CY 2018 wage index. The fourth
column shows the payment effects of
the CY 2018 case-mix weights. The fifth
column shows the effects the 0.97
percent reduction to the national,
standardized 60-day episode payment
amount to account for nominal case-mix
growth. The sixth column shows the
payment effects from the sunset of the
51747
rural add-on payment provision in
statute. The seventh column shows the
effects of the CY 2018 home health
payment update percentage.
The last column shows the combined
effects of all the policies in this final
rule. Overall, it is projected that
aggregate payments in CY 2018 will
decrease by 0.4 percent. As illustrated
in Table 25, the combined effects of all
of the changes vary by specific types of
providers and by location. We note that
some individual HHAs within the same
group may experience different impacts
on payments than others due to the
distributional impact of the CY 2018
wage index, the extent to which HHAs
had episodes in case-mix groups where
the case-mix weight decreased for CY
2018 relative to CY 2017, the percentage
of total HH PPS payments that were
subject to the low-utilization payment
adjustment (LUPA) or paid as outlier
payments, and the degree of Medicare
utilization. In addition, we clarify that
there are negative estimated impacts
attributed to the sunset of the rural addon provision for HHAs located in urban
areas as well as rural areas. This is due
to the fact that HHAs located in urban
areas provide services to patients
located in rural areas and payments are
based on the location of the beneficiary.
TABLE 25—ESTIMATED HHA IMPACTS BY FACILITY TYPE AND AREA OF THE COUNTRY, CY 2018
Number of
agencies
All Agencies ..............................................................................
CY 2018
wage
index 1
%
11,056
60-Day
episode
rate nominal
case-mix
reduction 3
%
Sunset of
rural add-on
HH payment
update
percentage 4
%
0.0
¥0.9
¥0.5
1.0
¥0.4
0.1
0.0
0.1
0.2
0.2
0.2
0.0
0.2
0.1
0.0
0.2
¥0.8
¥0.9
¥0.9
¥0.8
¥0.9
¥0.9
¥0.9
¥0.8
¥0.8
¥0.9
¥0.9
¥0.4
¥0.4
¥1.3
¥0.7
¥1.3
¥1.5
¥0.4
¥0.8
¥0.5
¥0.5
¥1.4
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
¥0.1
¥0.3
¥1.4
¥0.3
¥1.3
¥1.2
¥0.3
¥0.4
¥0.2
¥0.4
¥1.3
0.1
¥0.2
0.0
0.1
0.1
0.1
¥0.9
¥0.9
¥0.9
¥0.8
¥0.9
¥0.8
¥2.5
¥2.3
¥2.6
¥2.7
¥2.7
¥2.6
1.0
1.0
1.0
1.0
1.0
1.0
¥2.1
¥2.5
¥2.9
¥2.8
¥2.6
¥2.5
0.1
0.0
0.2
0.2
0.2
¥0.8
¥0.9
¥0.9
¥0.8
¥0.9
¥0.1
¥0.2
¥0.1
¥0.1
¥0.2
1.0
1.0
1.0
1.0
1.0
¥0.7
¥0.1
¥0.1
0.4
¥0.4
CY 2018
case-mix
weights 2
%
0.0
Total
%
Facility Type and Control
Free-Standing/Other Vol/NP .....................................................
Free-Standing/Other Proprietary ...............................................
Free-Standing/Other Government .............................................
Facility-Based Vol/NP ...............................................................
Facility-Based Proprietary .........................................................
Facility-Based Government .......................................................
Subtotal: Freestanding ..............................................................
Subtotal: Facility-based .............................................................
Subtotal: Vol/NP ........................................................................
Subtotal: Proprietary .................................................................
Subtotal: Government ...............................................................
1,110
8,724
318
634
81
189
10,152
904
1,744
8,805
507
0.0
0.0
¥0.3
0.0
¥0.3
0.0
0.0
0.0
0.0
0.0
¥0.2
asabaliauskas on DSKBBXCHB2PROD with RULES
Facility Type and Control: Rural
Free-Standing/Other Vol/NP .....................................................
Free-Standing/Other Proprietary ...............................................
Free-Standing/Other Government .............................................
Facility-Based Vol/NP ...............................................................
Facility-Based Proprietary .........................................................
Facility-Based Government .......................................................
265
832
224
285
42
142
0.2
¥0.1
¥0.4
¥0.4
¥0.1
¥0.2
Facility Type and Control: Urban
Free-Standing/Other Vol/NP .....................................................
Free-Standing/Other Proprietary ...............................................
Free-Standing/Other Government .............................................
Facility-Based Vol/NP ...............................................................
Facility-Based Proprietary .........................................................
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845
7,892
94
349
39
Frm 00073
Fmt 4701
¥0.9
0.0
¥0.3
0.1
¥0.5
Sfmt 4700
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TABLE 25—ESTIMATED HHA IMPACTS BY FACILITY TYPE AND AREA OF THE COUNTRY, CY 2018—Continued
Number of
agencies
Facility-Based Government .......................................................
CY 2018
wage
index 1
%
47
60-Day
episode
rate nominal
case-mix
reduction 3
%
Sunset of
rural add-on
HH payment
update
percentage 4
%
0.2
¥0.9
¥0.3
1.0
0.3
¥0.1
0.0
¥0.9
¥0.9
¥2.4
¥0.2
1.0
1.0
¥2.5
¥0.1
¥0.8
¥0.8
¥0.9
¥0.9
¥0.9
¥0.9
¥0.9
¥0.9
¥0.9
¥0.8
¥0.3
¥0.2
¥0.4
¥0.8
¥0.3
¥1.3
¥0.7
¥0.4
¥0.1
¥0.6
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
1.0
0.0
¥0.1
¥0.1
¥0.4
¥0.5
¥1.6
¥0.7
¥0.4
0.6
¥1.3
¥0.9
¥0.9
¥0.9
¥0.9
¥0.9
¥0.4
¥0.5
¥0.5
¥0.5
¥0.5
1.0
1.0
1.0
1.0
1.0
¥0.2
¥0.1
¥0.1
¥0.4
¥0.6
CY 2018
case-mix
weights 2
%
0.3
Total
%
Facility Location: Urban or Rural
Rural ..........................................................................................
Urban .........................................................................................
1,790
9,266
¥0.1
0.0
Facility Location: Region of the Country (Census Region)
New England .............................................................................
Mid Atlantic ................................................................................
East North Central ....................................................................
West North Central ...................................................................
South Atlantic ............................................................................
East South Central ....................................................................
West South Central ...................................................................
Mountain ....................................................................................
Pacific ........................................................................................
Other .........................................................................................
359
495
2,235
711
1,736
426
2,987
683
1,377
47
0.0
0.0
0.0
0.2
¥0.2
¥0.2
0.2
¥0.2
0.1
0.1
0.1
¥0.1
0.2
0.1
¥0.1
¥0.2
¥0.3
0.1
0.5
¥1.0
Facility Size (Number of 1st Episodes)
<100 episodes ...........................................................................
100 to 249 .................................................................................
250 to 499 .................................................................................
500 to 999 .................................................................................
1,000 or More ............................................................................
3,092
2,467
2,225
1,710
1,562
0.0
0.1
0.1
0.0
¥0.1
0.1
0.2
0.2
0.0
¥0.1
asabaliauskas on DSKBBXCHB2PROD with RULES
Source: CY 2016 Medicare claims data for episodes ending on or before December 31, 2016 for which we had a linked OASIS assessment.
1 The impact of the CY 2018 home health wage index is offset by the wage index budget neutrality factor described in section III.C.3 of this final rule.
2 The impact of the CY 2018 home health case-mix weights reflects the recalibration of the case-mix weights offset by the case-mix weights budget neutrality factor
described in section III.B of this final rule.
3 The 0.97 percent reduction to the national, standardized 60-day episode payment amount in CY 2018 is estimated to have a 0.9 percent impact on overall HH
PPS expenditures.
4 The CY 2018 home health payment update percentage reflects the home health payment update of 1 percent as described in section III.C.1 of this final rule.
REGION KEY:
New England = Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont.
Middle Atlantic = Pennsylvania, New Jersey, New York.
South Atlantic = Delaware, District of Columbia, Florida, Georgia, Maryland, North Carolina, South Carolina, Virginia, West Virginia.
East North Central = Illinois, Indiana, Michigan, Ohio, Wisconsin.
East South Central = Alabama, Kentucky, Mississippi, Tennessee.
West North Central = Iowa, Kansas, Minnesota, Missouri, Nebraska, North Dakota, South Dakota.
West South Central = Arkansas, Louisiana, Oklahoma, Texas.
Mountain = Arizona, Colorado, Idaho, Montana, Nevada, New Mexico, Utah, Wyoming.
Pacific = Alaska, California, Hawaii, Oregon, Washington.
Other = Guam, Puerto Rico, Virgin Islands.
The following is a summary of the
public comments received on the
‘‘Regulatory Impact Analysis’’ and our
responses:
Comment: A commenter requested
that CMS provide the impact analyses of
the case-mix weight changes that are
annually proposed.
Response: The analyses of the annual
case-mix weight changes are included in
Table 25 in the fourth column titled,
‘‘CY 2018 Case-Mix Weights’’.
Comment: A commenter stated that
when isolating the case mix changes
from CY2017 to the CY2018 proposed
rule, they are seeing an average impact
of ¥0.58% which differs from the CMS
projected 0.0 percent in Table 54 of the
proposed rule. This analysis is for the
case-mix components only (weights and
budget neutrality factor), and excludes
all other components such as wage
index, nominal CM reduction, sunset of
rural add-on, and the payment update
percentage. The commenter requested
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an explanation of the apparent
discrepancy.
Response: We estimate that all HHAs
nationwide will see a decrease in
average case-mix between CY 2017 and
CY 2018 of 1.6 percent due to
recalibration of the case-mix weights
(hence the BN factor of 1.6 percent). In
increasing the base rate by 1.6 percent
to offset the decrease in average casemix, those HHAs that have a decrease in
average case-mix of less than 1.6 percent
between CY 2017 and CY 2018 will see
a small increase in payment for CY 2018
due to the case-mix weights budget
neutrality factor. Those HHAs that have
a decrease in average case-mix of more
than 1.6 percent due to the case-mix
weight recalibration between CY 2017
and CY 2018 will see a small decrease
in payment for CY 2018 (generally
proportional to the decrease in average
case-mix above and beyond ¥1.6
percent). The adjustment for case-mix
normalization is budget neutral in the
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aggregate but not so for individual
HHAs.
2. HHVBP Model
Table 26 displays our analysis of the
distribution for possible payment
adjustments at the 3-percent, 5-percent,
6-percent, 7-percent, and 8-percent rates
that are being used in the Model using
CY 2015 baseline data and CY 2016 PY
1 data for OASIS-based measures,
claims-based hospitalization and
Emergency Department (ED) measures,
and HHCAHPS data. The estimated
impacts account for the minimum 40
HHCAHPS completed surveys policy,
beginning with PY 1, as finalized in this
rule. For PY 1 and 2, we show the
impacts based on ten OASIS quality
measures (9 OASIS quality measures
were used for PY 3 through 5 to
represent the removal of the Drug
Education measure), two claims-based
measures in QIES, five HHCAHPS
measures, and the three new measures
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beneficiaries that reside in rural areas
and HHA organizational status. HHAs
with a higher proportion of duallyeligible beneficiaries and HHAs whose
beneficiaries have higher acuity tend to
have better performance.
The payment adjustment percentages
are calculated at the state and size
cohort level. Hence, the values of each
separate analysis in the tables reflect the
baseline year of 2015 and the
performance year of 2016. There are
1,622 Medicare-certified HHAs in the
nine selected states that have a
sufficient number of measures to receive
a payment adjustment in the Model. We
note in Table 28, that at the time of our
analysis, seven of the 1,622 Medicarecertified HHAs were missing
information needed for the
stratifications in the table. Not all
Medicare-certified HHAs in the nine
states have a payment adjustment
because some HHAs are servicing too
small of a population to report an
adequate number of measures to
calculate a TPS. However, as noted
previously, our updated analysis found
that the number of such HHAs was not
affected by the proposed minimum 40
HHCAHPS survey policy, which we are
finalizing.
Additional analysis (see Table 29) was
conducted to illustrate the effect of the
finalized policy to require 40 or more
completed HHCAHPS surveys versus 20
or more completed HHCAHPS surveys.
We include information on average
statewide TPS by size of the HHA. The
percentage difference in the average TPS
across all larger-volume HHAs for each
state ranges from ¥0.3 percent through
1.8 percent and the majority of states are
close to zero.
be one cohort that will include all the
HHAs in that state. As indicated in
Table 27, Arizona, Maryland, North
Carolina, Tennessee and Washington
will only have one cohort while Florida,
Iowa, Massachusetts, and Nebraska will
have both a smaller-volume cohort and
a larger-volume cohort. For example,
Iowa has 26 HHAs exempt from the
requirement that their beneficiaries
complete HHCAHPS surveys because
they provided HHA services to fewer
than 60 beneficiaries in CY 2015.
Therefore, 26 HHAs competed in Iowa’s
smaller-volume cohort for the 2016
performance year under the Model.
Using CY 2015 baseline year data and
CY 2016 PY 1 data and the maximum
payment adjustment for PY 1 of 3percent (as applied in CY 2018), based
on the ten OASIS quality measures, two
claims-based measures in QIES, the five
HHCAHPS measures, and the three new
measures, the smaller-volume HHAs in
Iowa have a mean payment adjustment
of ¥0.1 percent (Table 27). Ten percent
of HHAs in the smaller-volume cohort
will be subject to payment adjustments
of more than minus 1.1 percent (¥1.1
percent), the lowest 10th percentile. The
next columns provide the distribution of
scores by percentile; we see that the
cohort payment adjustment distribution
for HHAs in Iowa in the smaller-volume
cohort ranges from ¥1.1 percent at the
10th percentile to +1.5 percent at the
90th percentile, while the cohort
payment adjustment distribution
median is ¥0.3 percent.
Table 28 provides the payment
adjustment distribution based on agency
size, proportion of dually-eligible
beneficiaries, average case mix (using
the average case-mix for non-LUPA
episodes), the proportion of the HHA’s
(using the October 2016 and January
2017 submission data), using the QIES
Roll Up File data in the same manner as
they will be in the Model. HHAs were
classified as being in the smaller or
larger volume cohort using the 2015
Quality Episode File, as updated for this
final rule, which is created using OASIS
assessments. The basis of the payment
adjustment was derived from complete
2015 claims data. We note that this
impact analysis is based on the
aggregate value of all nine states.
Table 27 displays our analysis of the
distribution of possible payment
adjustments based on the same CY 2015
baseline data and 2016 PY 1 data used
to calculate Table 26, providing
information on the estimated impact of
the finalized policies in this final rule.
Note that all Medicare-certified HHAs
that provide services in Massachusetts,
Maryland, North Carolina, Florida,
Washington, Arizona, Iowa, Nebraska,
and Tennessee are required to compete
in this Model. This analysis reflects that
only HHAs that have data for at least
five measures that meet the
requirements of § 484.305, as amended
by this final rule, will be included in the
LEF and will have a payment
adjustment calculated. Value-based
incentive payment adjustments for the
estimated 1,600 plus HHAs in the
selected states that will compete in the
HHVBP Model are stratified by size as
described in section IV.B. of the CY
2017 HH PPS final rule. As finalized in
section IV.B. of the CY 2017 HH PPS
final rule, there must be a minimum of
eight HHAs in any cohort.
Those HHAs that are in states that do
not have at least eight smaller-volume
HHAs do not have a separate smallervolume cohort and thus there will only
TABLE 26—ADJUSTMENT DISTRIBUTION BY PERCENTILE LEVEL OF QUALITY TOTAL PERFORMANCE SCORE AT DIFFERENT
MODEL PAYMENT ADJUSTMENT RATES
[Percentage]*
Range
(%)
Payment adjustment distribution
3%
5%
6%
7%
8%
Payment
Payment
Payment
Payment
Payment
Adjustment
Adjustment
Adjustment
Adjustment
Adjustment
For
For
For
For
For
Performance
Performance
Performance
Performance
Performance
Year
Year
Year
Year
Year
1
2
3
4
5
of
of
of
of
of
the
the
the
the
the
Model .....
Model .....
Model** ..
Model** ..
Model** ..
2.8
4.6
5.8
6.7
7.7
10%
¥1.3
¥2.2
¥2.8
¥3.2
¥3.7
20%
30%
¥0.9
¥1.6
¥1.9
¥2.2
¥2.5
¥0.6
¥1.0
¥1.3
¥1.5
¥1.7
40%
Median
¥0.4
¥0.6
¥0.7
¥0.9
¥1.0
¥0.1
¥0.1
¥0.2
¥0.2
¥0.2
60%
70%
0.2
0.3
0.4
0.5
0.5
0.5
0.8
1.0
1.2
1.4
80%
0.8
1.4
1.7
1.9
2.2
90%
1.4
2.4
3.0
3.5
4.0
asabaliauskas on DSKBBXCHB2PROD with RULES
* Based on measure performance data from Performance Year 1 (January 1, 2016 to December 31, 2016), the baseline year (January 1, 2015 to December 31,
2015), and home health Medicare claims data from 2015.
** For Performance Years 3, 4, and 5, the payment adjustment rate simulation incorporated the removal of the Drug Education measure.
TABLE 27—HHA COHORT PAYMENT ADJUSTMENT DISTRIBUTIONS BY STATE/COHORT
[Based on a 3-percent payment adjustment]
Number
of HHAs
State
Average
payment
adj. %
10%
20%
30%
40%
50%
60%
70%
80%
90%
HHA Cohort in States with no small cohorts (percent)
AZ ....................................................................
MD ...................................................................
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0.1
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¥0.8
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¥0.9
¥0.8
Sfmt 4700
¥0.7
¥0.6
¥0.4
¥0.4
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0.1
07NOR2
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0.4
0.5
0.5
0.7
0.8
1.1
1.0
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TABLE 27—HHA COHORT PAYMENT ADJUSTMENT DISTRIBUTIONS BY STATE/COHORT—Continued
[Based on a 3-percent payment adjustment]
Average
payment
adj. %
Number
of HHAs
State
NC ...................................................................
TN ....................................................................
WA ...................................................................
10%
¥0.1
¥0.1
¥0.1
163
123
57
20%
¥1.3
¥1.3
¥1.0
30%
¥0.9
¥1.0
¥0.8
40%
¥0.5
¥0.7
¥0.6
50%
¥0.2
¥0.4
¥0.2
60%
70%
80%
90%
0.0
¥0.1
¥0.2
0.2
0.2
0.0
0.4
0.3
0.3
0.7
0.6
0.3
0.9
1.0
0.8
¥0.2
¥0.3
¥0.8
0.2
0.6
0.0
¥0.4
0.6
0.9
0.4
0.3
1.1
1.5
0.8
0.8
1.2
2.2
1.5
2.3
2.7
0.0
¥0.3
¥0.3
0.1
0.2
0.0
0.0
0.3
0.6
0.3
0.3
0.7
1.0
0.7
0.6
0.9
1.7
1.2
1.1
1.2
Smaller-volume HHA Cohort in states with small cohort (percent)
FL ....................................................................
IA .....................................................................
MA ...................................................................
NE ...................................................................
82
26
16
16
0.1
¥0.1
¥0.4
0.2
¥1.6
¥1.1
¥1.7
¥1.6
¥1.3
¥1.0
¥1.5
¥1.5
¥1.0
¥0.9
¥1.5
¥1.0
¥0.6
¥0.6
¥1.1
¥0.1
Large-volume HHA Cohort in states with small cohort (percent)
FL ....................................................................
IA .....................................................................
MA ...................................................................
NE ...................................................................
706
99
124
45
0.1
¥0.2
¥0.2
0.0
¥1.2
¥1.4
¥1.5
¥1.4
¥0.8
¥1.1
¥1.1
¥0.7
¥0.5
¥0.8
¥0.8
¥0.6
¥0.3
¥0.5
¥0.6
¥0.2
Notes: Based on measure performance data from Performance Year 1 (January 1, 2016 to December 31, 2016), the baseline year (January 1, 2015 to December
31, 2015), and home health Medicare claims data from 2015.
TABLE 28—PAYMENT ADJUSTMENT DISTRIBUTIONS BY CHARACTERISTICS
[Based on a 3-percent payment adjustment]1
Number of
HHAs
Cohort
Small HHA (<60 patients in CY 2015) ............
Large HHA (≥60 patients in CY 2015) ............
Low % Dually-Eligible .....................................
Medium % Dually-Eligible ...............................
High % Dually-Eligible .....................................
Low Acuity .......................................................
Mid Acuity ........................................................
High Acuity ......................................................
All non-rural beneficiaries ...............................
Up to 35% rural beneficiaries .........................
Over 35% rural beneficiaries ..........................
Non-Profit HHAs ..............................................
For-Profit HHAs ...............................................
Government HHAs ..........................................
Freestanding ...................................................
Facility-based ..................................................
Average payment adj. %
150
1,465
403
809
403
403
809
403
956
384
275
295
1,211
109
1,460
155
0.0
0.0
0.1
¥0.1
0.1
¥0.3
0.0
0.4
0.1
¥0.1
¥0.1
0.1
0.0
¥0.2
0.0
¥0.1
10%
20%
¥1.6
¥1.2
¥1.1
¥1.3
¥1.5
¥1.6
¥1.2
¥1.1
¥1.3
¥1.3
¥1.3
¥1.1
¥1.4
¥1.1
¥1.3
¥1.3
30%
¥1.4
¥0.9
¥0.8
¥0.9
¥1.1
¥1.2
¥0.9
¥0.6
¥0.9
¥0.9
¥1.0
¥0.8
¥1.0
¥0.9
¥0.9
¥0.9
40%
¥1.0
¥0.6
¥0.5
¥0.6
¥0.8
¥1.0
¥0.6
¥0.3
¥0.6
¥0.6
¥0.7
¥0.5
¥0.6
¥0.8
¥0.6
¥0.6
50%
¥0.6
¥0.3
¥0.2
¥0.4
¥0.5
¥0.7
¥0.4
0.0
¥0.3
¥0.3
¥0.4
¥0.2
¥0.4
¥0.5
¥0.4
¥0.3
60%
¥0.3
¥0.1
0.1
¥0.1
¥0.1
¥0.4
¥0.1
0.3
0.0
¥0.1
¥0.2
0.0
¥0.1
¥0.3
¥0.1
¥0.1
0.2
0.2
0.3
0.1
0.3
¥0.1
0.1
0.6
0.3
0.1
0.0
0.3
0.2
0.0
0.2
0.1
70%
80%
0.7
0.5
0.6
0.4
0.7
0.2
0.4
0.9
0.6
0.4
0.2
0.6
0.5
0.1
0.5
0.3
90%
1.2
0.8
0.9
0.6
1.3
0.6
0.7
1.4
1.0
0.7
0.7
0.9
0.8
0.4
0.8
0.7
2.2
1.4
1.4
1.0
2.1
1.1
1.2
2.1
1.7
1.0
1.2
1.3
1.5
1.0
1.5
1.0
Notes:
1 Rural beneficiaries identified based on the CBSA code reported on the claim. Acuity is based on the average case-mix weight for non-LUPA episodes. Low acuity
is defined as the bottom 25 percent (among HHVBP Model participants); mid-acuity is the middle 50 percent and high acuity is the highest 25 percent. Note that at
the time of the analysis, seven HHAs were missing information needed for the stratifications in this table.
TABLE 29—IMPACT OF CHANGING MINIMUM REQUIRED SAMPLE SIZE FOR HHCAHPS PERFORMANCE MEASURES ON
AVERAGE TPS AND PAYMENT ADJUSTMENT RANGE*
Average TPS
HHA
count
State
20
Minimum
40
Minimum
Minimum payment
adjustment
Difference
%
Difference
20
Minimum
(%)
40
Minimum
(%)
Maximum payment
adjustment
20
Minimum
(%)
40
Minimum
(%)
asabaliauskas on DSKBBXCHB2PROD with RULES
Larger-volume HHAS
AZ ..............................................................
FL ..............................................................
IA ...............................................................
MA .............................................................
MD .............................................................
NC .............................................................
NE .............................................................
TN ..............................................................
WA .............................................................
107
706
99
124
50
163
45
119
57
42.160
39.110
43.191
41.380
49.179
45.798
42.252
47.462
51.840
42.924
39.731
43.186
41.256
49.549
46.187
43.028
47.540
51.712
0.765
0.621
¥0.005
¥0.125
0.370
0.390
0.776
0.078
¥0.128
1.8
1.6
0.0
¥0.3
0.7
0.8
1.8
0.2
¥0.2
¥2.3
¥2.5
¥2.1
¥2.6
¥1.3
¥2.1
¥2.1
¥2.5
¥1.5
¥2.3
¥2.5
¥2.1
¥2.5
¥1.3
¥2.1
¥2.1
¥2.3
¥1.6
2.8
3.0
2.0
2.4
2.0
2.9
2.6
1.6
1.1
2.7
3.0
2.4
2.5
2.0
2.9
2.4
2.1
1.1
Total ...................................................
1,470
....................
....................
....................
................
................
................
....................
....................
0.0
0.0
0.0
0.0
¥1.8
¥2.3
¥1.8
¥1.7
¥1.9
¥2.3
¥1.8
¥1.7
1.0
2.9
2.2
2.3
1.0
2.9
2.2
2.3
Smaller-volume HHAS
AZ ..............................................................
FL ..............................................................
IA ...............................................................
MA .............................................................
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42.810
38.663
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0.000
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TABLE 29—IMPACT OF CHANGING MINIMUM REQUIRED SAMPLE SIZE FOR HHCAHPS PERFORMANCE MEASURES ON
AVERAGE TPS AND PAYMENT ADJUSTMENT RANGE*—Continued
Average TPS
HHA
count
State
20
Minimum
40
Minimum
Minimum payment
adjustment
Difference
%
Difference
20
Minimum
(%)
40
Minimum
(%)
Maximum payment
adjustment
20
Minimum
(%)
40
Minimum
(%)
MD .............................................................
NE .............................................................
TN ..............................................................
1
16
4
61.135
37.485
39.983
61.135
37.485
39.983
0.000
0.000
0.000
0.0
0.0
0.0
0.8
¥2.6
¥1.8
0.8
¥2.6
¥1.8
0.8
3.0
1.9
0.8
3.0
1.9
Total ...................................................
152
....................
....................
....................
................
................
................
....................
....................
Total ...................................................
1,622
....................
....................
....................
................
................
................
....................
....................
* OASIS, claims and HHCAHPS measures run from January 1, 2016 to December 31, 2016 for Performance Year 1. The baseline year is January 1, 2015 to December 31, 2015. Payment based on 2015 Medicare home health claims data. North Carolina and Washington did not have any smaller-volume HHAs.
3. HH QRP
Failure to submit data required under
section 1895(b)(3)(B)(v) of the Act will
result in the reduction of the annual
update to the standard federal rate for
discharges occurring during such fiscal
year by 2 percentage points for any HHA
that does not comply with the
requirements established by the
Secretary. At the time that this analysis
was prepared, 1,206, or approximately
9.9 percent, of the 12,149 active
Medicare-certified HHAs, did not
receive the full annual percentage
increase for CY 2017 because they did
not meet the requirements of the HH
QRP. Information is not available to
determine the precise number of HHAs
that will not meet the requirements to
receive the full annual percentage
increase for the CY 2018 payment
determination.
As noted in section VII.B. of this final
rule, the net effect of our provisions is
an estimated decrease in cost associated
with changes to the HH QRP on average
of $12,016.33 per HHA annually, or
$145,986,343.50 for all HHAs annually.
Comment: A commenter stated that
CMS had underestimated the cost of
changes to the OASIS, adding that CMS
had not considered training and
opportunity costs related to data set
changes.
Response: Our burden estimates
reflect the burden on data submission.
We intend to provide educational
resources on the OASIS changes,
including training and guidance, to
providers at no cost.
transfers and costs associated with the
HH PPS provisions of this final rule.
Table 30 provides our best estimate of
the decrease in Medicare payments
under the HH PPS as a result of the
changes presented in this final rule for
the HH PPS provisions in CY 2018.
Table 31 provides our best estimates of
the changes associated with the HH QRP
provisions.
TABLE 30—ACCOUNTING STATEMENT:
HH PPS CLASSIFICATION OF ESTIMATED TRANSFERS, FROM CY 2017
TO 2018
D. Accounting Statements and Tables
As required by OMB Circular A–4
(available at https://
www.whitehouse.gov/omb/circulars_
a004_a-4), in Table 30, we have
prepared an accounting statement
showing the classification of the
Category
Annualized Monetized
Transfers.
From Whom to
Whom?
Transfers
¥$80 million.
Federal Government
to HHAs.
TABLE 31—ACCOUNTING STATEMENT: HH QRP CLASSIFICATION OF ESTIMATED COSTS, FROM CY 2018 TO 2019
Category
Costs
Annualized Monetized Net Burden for HHAs Submission of the OASIS
F. Conclusion
payments to HHAs for CY 2018. The
¥$80 million impact reflects the effects
of a 0.5 percent reduction in payments
due to the sunset of the rural add-on
provision ($100 million decrease), a 1
percent CY 2018 HH payment update
percentage ($190 million increase), and
a 0.9 percent decrease in payments due
to the 0.97 percent reduction to the
national, standardized 60-day episode
payment rate in CY 2017 to account for
nominal case-mix growth ($170 million
decrease).
1. HH PPS
2. HHVBP Model
In conclusion, we estimate that the
net impact of the HH PPS policies in
this final rule is a decrease of 0.4
percent, or $80 million, in Medicare
In conclusion, we estimate there will
be no net impact (to include either a net
increase or reduction in payments) in
this final rule in Medicare payments to
E. Reducing Regulation and Controlling
Regulatory Costs
asabaliauskas on DSKBBXCHB2PROD with RULES
¥$146.0 million.
Executive Order 13771, entitled
Reducing Regulation and Controlling
Regulatory Costs (82 FR 9339), was
issued on January 30, 2017. This final
rule is considered an E.O. 13771
deregulatory action. Details on the
estimated cost savings of this proposed
rule can be found in the rule’s PRA and
economic analysis.
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20:38 Nov 06, 2017
Jkt 244001
PO 00000
Frm 00077
Fmt 4701
Sfmt 4700
HHAs competing in the HHVBP Model
for CY 2018. However, the overall
economic impact of the HHVBP Model
is an estimated $378 million in total
savings from a reduction in unnecessary
hospitalizations and SNF usage as a
result of greater quality improvements
in the home health industry over the life
of the HHVBP Model.
3. HH QRP
In conclusion, for CY 2019 we
estimate that there will be a total
decrease in costs of $145,986,343.50
associated with the changes to the HH
QRP.
This analysis, together with the
remainder of this preamble, provides
afinal Regulatory Flexibility Analysis.
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Federal Register / Vol. 82, No. 214 / Tuesday, November 7, 2017 / Rules and Regulations
VIII. Federalism Analysis
Executive Order 13132 on Federalism
(August 4, 1999) establishes certain
requirements that an agency must meet
when it promulgates a final rule that
imposes substantial direct requirement
costs on state and local governments,
preempts state law, or otherwise has
Federalism implications. We have
reviewed this final rule under the
threshold criteria of Executive Order
13132, Federalism, and have
determined that it will not have
substantial direct effects on the rights,
roles, and responsibilities of states, local
or tribal governments.
In accordance with the provisions of
Executive Order 12866, this final rule
was reviewed by the Office of
Management and Budget.
List of Subjects for 42 CFR Part 484
Health facilities, Health professions,
Medicare, Reporting and recordkeeping
requirements.
For the reasons set forth in the
preamble, the Centers for Medicare &
Medicaid Services amends 42 CFR part
484 as set forth below:
PART 484—HOME HEALTH SERVICES
1. The authority citation for part 484
continues to read as follows:
■
Authority: Secs 1102 and 1871 of the Act
(42 U.S.C. 1302 and 1395(hh)) unless
otherwise indicated.
2. Section 484.250 is amended by
revising paragraph (a)(1) and adding
paragraphs (d) through (f) to read as
follows:
■
asabaliauskas on DSKBBXCHB2PROD with RULES
§ 484.250
Patient assessment data.
(a) * * *
(1) The OASIS data described at
§ 484.55(b) and (d) for CMS to
administer the payment rate
methodologies described in §§ 484.215,
484.220, 484. 230, 484.235, and 484.240;
and to meet the quality reporting
requirements of section 1895(b)(3)(B)(v)
of the Act.
*
*
*
*
*
(d) Exceptions and extension
requirements. (1) A HHA may request
and CMS may grant exceptions or
extensions to the reporting requirements
under section 1895(b)(3)(B)(v) of the Act
for one or more quarters, when there are
certain extraordinary circumstances
beyond the control of the HHA.
(2) A HHA may request an exception
or extension within 90 days of the date
VerDate Sep<11>2014
20:38 Nov 06, 2017
Jkt 244001
that the extraordinary circumstances
occurred by sending an email to CMS
HHAPU reconsiderations at
HHAPUReconsiderations@cms.hhs.gov
that contains all of the following
information:
(i) HHA CMS Certification Number
(CCN).
(ii) HHA Business Name.
(iii) HHA Business Address.
(iv) CEO or CEO-designated personnel
contact information including name,
telephone number, title, email address,
and mailing address (the address must
be a physical address, not a post office
box).
(v) HHA’s reason for requesting the
exception or extension.
(vi) Evidence of the impact of
extraordinary circumstances, including,
but not limited to, photographs,
newspaper, and other media articles.
(vii) Date when the HHA believes it
will be able to again submit data under
section 1895(b)(3)(B)(v) of the Act and a
justification for the proposed date.
(3) Except as provided in paragraph
(d)(4) of this section, CMS will not
consider an exception or extension
request unless the HHA requesting such
exception or extension has complied
fully with the requirements in this
paragraph (d).
(4) CMS may grant exceptions or
extensions to HHAs without a request if
it determines that one or more of the
following has occurred:
(i) An extraordinary circumstance
affects an entire region or locale.
(ii) A systemic problem with one of
CMS’s data collection systems directly
affected the ability of a HHA to submit
data under section 1895(b)(3)(B)(v) of
the Act.
(e) Reconsideration. (1) HHAs that do
not meet the quality reporting
requirements under section
1895(b)(3)(B)(v) of the Act for a program
year will receive a letter of noncompliance via the United States Postal
Service and notification in CASPER. An
HHA may request reconsideration no
later than 30 calendar days after the date
identified on the letter of noncompliance.
(2) Reconsideration requests may be
submitted to CMS by sending an email
to CMS HHAPU reconsiderations at
HHAPureConsiderations@cms.hhs.gov
containing all of the following
information:
(i) HHA CCN.
(ii) HHA Business Name.
PO 00000
Frm 00078
Fmt 4701
Sfmt 9990
(iii) HHA Business Address.
(iv) CEO or CEO-designated personnel
contact information including name,
telephone number, title, email address,
and mailing address (the address must
be a physical address, not a post office
box).
(v) CMS identified reason(s) for noncompliance from the non-compliance
letter.
(vi) Reason(s) for requesting
reconsideration, including all
supporting documentation.
(3) CMS will not consider an
exception or extension request unless
the HHA has complied fully with the
requirements in paragraph (e)(2) of this
section.
(4) CMS will make a decision on the
request for reconsideration and provide
notice of the decision to the HHA
through CASPER and via letter sent via
the United States Postal Service.
(f) Appeals. (1) A HHA that is
dissatisfied with CMS’ decision on a
request for reconsideration submitted
under paragraph (e) of this section may
file an appeal with the Provider
Reimbursement Review Board (PRRB)
under 42 CFR part 405, subpart R.
(2) [Reserved]
3. Section 484.305 is amended by
revising the definition of ‘‘Applicable
measure’’ to read as follows:
■
§ 484.305
Definitions.
*
*
*
*
*
Applicable measure means a measure
for which a competing HHA has
provided a minimum of—
(1) Twenty home health episodes of
care per year for the OASIS-based
measures;
(2) Twenty home health episodes of
care per year for the claims-based
measures; or
(3) Forty completed surveys for the
HHCAHPS measures.
*
*
*
*
*
Dated: October 23, 2017.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
Dated: October 24, 2017.
Eric D. Hargan,
Acting Secretary, Department of Health and
Human Services.
[FR Doc. 2017–23935 Filed 11–1–17; 4:15 pm]
BILLING CODE 4120–01–P
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Agencies
[Federal Register Volume 82, Number 214 (Tuesday, November 7, 2017)]
[Rules and Regulations]
[Pages 51676-51752]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-23935]
[[Page 51675]]
Vol. 82
Tuesday,
No. 214
November 7, 2017
Part II
Department of Health and Human Services
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Centers for Medicare & Medicaid Services
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42 CFR Part 484
Medicare and Medicaid Programs; CY 2018 Home Health Prospective
Payment System Rate Update and CY 2019 Case-Mix Adjustment Methodology
Refinements; Home Health Value-Based Purchasing Model; and Home Health
Quality Reporting Requirements; Final Rule
Federal Register / Vol. 82 , No. 214 / Tuesday, November 7, 2017 /
Rules and Regulations
[[Page 51676]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 484
[CMS-1672-F]
RIN 0938-AT01
Medicare and Medicaid Programs; CY 2018 Home Health Prospective
Payment System Rate Update and CY 2019 Case-Mix Adjustment Methodology
Refinements; Home Health Value-Based Purchasing Model; and Home Health
Quality Reporting Requirements
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This final rule updates the home health prospective payment
system (HH PPS) payment rates, including the national, standardized 60-
day episode payment rates, the national per-visit rates, and the non-
routine medical supply (NRS) conversion factor, effective for home
health episodes of care ending on or after January 1, 2018. This rule
also: Updates the HH PPS case-mix weights using the most current,
complete data available at the time of rulemaking; implements the third
year of a 3-year phase-in of a reduction to the national, standardized
60-day episode payment to account for estimated case-mix growth
unrelated to increases in patient acuity (that is, nominal case-mix
growth) between calendar year (CY) 2012 and CY 2014; and discusses our
efforts to monitor the potential impacts of the rebasing adjustments
that were implemented in CY 2014 through CY 2017. In addition, this
rule finalizes changes to the Home Health Value-Based Purchasing
(HHVBP) Model and to the Home Health Quality Reporting Program (HH
QRP). We are not finalizing the implementation of the Home Health
Groupings Model (HHGM) in this final rule.
DATES: These regulations are effective on January 1, 2018.
FOR FURTHER INFORMATION CONTACT:
For general information about the Home Health Prospective Payment
System (HH PPS), please send your inquiry via email to:
HomehealthPolicy@cms.hhs.gov.
For information about the Home Health Value-Based Purchasing
(HHVBP) Model, please send your inquiry via email to:
HHVBPquestions@cms.hhs.gov.
Contact Joan Proctor, (410) 786-0949 for information about the Home
Health Quality Reporting Program (HH QRP).
SUPPLEMENTARY INFORMATION: Wage index addenda will be available only
through the internet on the CMS Web site at: https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/HomeHealthPPS/coding_billing.html.
Table of Contents
I. Executive Summary
A. Purpose
B. Summary of the Major Provisions
C. Summary of Costs and Benefits
II. Background
A. Statutory Background
B. Current System for Payment of Home Health Services
C. Updates to the Home Health Prospective Payment System
D. Report to Congress: Home Health Study on Access to Care for
Vulnerable Patient Populations and Subsequent Research and Analyses
III. Provisions of the Proposed Rule: Payment Under the Home Health
Prospective Payment System (HH PPS) and Responses to Comments
A. Monitoring for Potential Impacts--Affordable Care Act
Rebasing Adjustments
B. CY 2018 HH PPS Case-Mix Weights
C. CY 2018 Home Health Payment Rate Update
D. Payments for High-Cost Outliers Under the HH PPS
E. Proposed Implementation of the Home Health Groupings Model
(HHGM) for CY 2019
IV. Provisions of the Home Health Value-Based Purchasing (HHVBP)
Model and Responses to Comments
A. Background
B. Quality Measures
C. Quality Measures for Future Consideration
V. Updates to the Home Health Care Quality Reporting Program (HH
QRP)
A. Background and Statutory Authority
B. General Considerations Used for the Selection of Quality
Measures for the HH QRP
C. Accounting for Social Risk Factors in the HH QRP
D. Removal From OASIS
E. Collection of Standardized Patient Assessment Data Under the
HH QRP
F. HH QRP Quality Measures Beginning With the CY 2020 HH QRP
G. HH QRP Quality Measures and Measure Concepts Under
Consideration for Future Years
H. Standardized Patient Assessment Data
I. Form, Manner, and Timing of Data Submission Under the HH QRP
J. Other Provisions for the CY 2019 HH QRP and Subsequent Years
K. Policies Regarding Public Display of Quality Measure Data for
the HH QRP
L. Mechanism for Providing Confidential Feedback Reports to HHAs
M. Home Health Care CAHPS[supreg] Survey (HHCAHPS)
VI. Collection of Information Requirements
A. Statutory Requirement for Solicitation of Comments
B. Collection of Information Requirements for the HH QRP
C. Submission of PRA-Related Comments
VII. Regulatory Impact Analysis
A. Statement of Need
B. Overall Impact
C. Detailed Economic Analysis
D. Accounting Statement and Table
E. Reducing Regulation and Controlling Regulatory Costs
F. Conclusion
VIII. Federalism Analysis
Regulation Text
Acronyms
In addition, because of the many terms to which we refer by
abbreviation in this final rule, we are listing these abbreviations and
their corresponding terms in alphabetical order below:
ACH LOS Acute Care Hospital Length of Stay
ADL Activities of Daily Living
AM-PAC Activity Measure for Post-Acute Care
APR DRG All-Patient Refined Diagnosis-Related Group
APU Annual Payment Update
ASPE Assistant Secretary for Planning and Evaluation
BBA Balanced Budget Act of 1997, Public Law 105-33
BBRA Medicare, Medicaid, and SCHIP Balanced Budget Refinement Act of
1999, (Pub. L. 106-113)
BIMS Brief Interview for Mental Status
BLS Bureau of Labor Statistics
CAD Coronary Artery Disease
CAH Critical Access Hospital
CAM Confusion Assessment Method
CARE Continuity Assessment Record and Evaluation
CASPER Certification and Survey Provider Enhanced Reports
CBSA Core-Based Statistical Area
CCN CMS Certification Number
CHF Congestive Heart Failure
CMI Case-Mix Index
CMP Civil Money Penalty
CMS Centers for Medicare & Medicaid Services
CoPs Conditions of Participation
COPD Chronic Obstructive Pulmonary Disease
CVD Cardiovascular Disease
CY Calendar Year
DM Diabetes Mellitus
DRA Deficit Reduction Act of 2005, Public Law 109-171, enacted
February 8, 2006
DRG Diagnosis-Related Group
DTI Deep Tissue Injury
EOC End of Care
FDL Fixed Dollar Loss
FI Fiscal Intermediaries
FR Federal Register
FY Fiscal Year
HAVEN Home Assessment Validation and Entry System
HCC Hierarchical Condition Categories
HCIS Health Care Information System
HH Home Health
HHA Home Health Agency
[[Page 51677]]
HHCAHPS Home Health Care Consumer Assessment of Healthcare Providers
and Systems Survey
HH PPS Home Health Prospective Payment System
HHGM Home Health Groupings Model
HHQRP Home Health Quality Reporting Program
HHRG Home Health Resource Group
HHVBP Home Health Value-Based Purchasing
HIPPS Health Insurance Prospective Payment System
HVBP Hospital Value-Based Purchasing
IADL Instrumental Activities of Daily Living
ICD-9-CM International Classification of Diseases, Ninth Revision,
Clinical Modification
ICD-10-CM International Classification of Diseases, Tenth Revision,
Clinical Modification
IH Inpatient Hospitalization
IMPACT Act Improving Medicare Post-Acute Care Transformation Act of
2014 (Pub. L. 113-185)
IPPS [Acute Care Hospital] Inpatient Prospective Payment System
IPR Interim Performance Report
IRF Inpatient Rehabilitation Facility
IRF-PAI IRF Patient Assessment Instrument
IV Intravenous
LCDS LTCH CARE Data Set
LEF Linear Exchange Function
LTCH Long-Term Care Hospital
LUPA Low-Utilization Payment Adjustment
MACRA Medicare Access and CHIP Reauthorization Act of 2015
MAP Measure Applications Partnership
MDS Minimum Data Set
MFP Multifactor productivity
MMA Medicare Prescription Drug, Improvement, and Modernization Act
of 2003, Public Law 108-173, enacted December 8, 2003
MSA Metropolitan Statistical Area
MSS Medical Social Services
NQF National Quality Forum
NQS National Quality Strategy
NRS Non-Routine Supplies
OASIS Outcome and Assessment Information Set
OBRA Omnibus Budget Reconciliation Act of 1987, Public Law 100-2-3,
enacted December 22, 1987
OCESAA Omnibus Consolidated and Emergency Supplemental
Appropriations Act, Public Law 105-277, enacted October 21, 1998
OES Occupational Employment Statistics
OIG Office of Inspector General
OLS Ordinary Least Squares
OT Occupational Therapy
OMB Office of Management and Budget
PAC Post-Acute Care
PAC-PRD Post-Acute Care Payment Reform Demonstration
PAMA Protecting Access to Medicare Act of 2014
PEP Partial Episode Payment Adjustment
PHQ-2 Patient Health Questionnaire-2
PPOC Primary Point of Contact
PPS Prospective Payment System
PRA Paperwork Reduction Act
PRRB Provider Reimbursement Review Board
PT Physical Therapy
PY Performance Year
QAP Quality Assurance Plan
QIES Quality Improvement Evaluation System
QRP Quality Reporting Program
RAP Request for Anticipated Payment
RF Renal Failure
RFA Regulatory Flexibility Act, Public Law 96--354
RHHIs Regional Home Health Intermediaries
RIA Regulatory Impact Analysis
ROC Resumption of Care
SAF Standard Analytic File
SLP Speech-Language Pathology
SN Skilled Nursing
SNF Skilled Nursing Facility
SOC Start of Care
SSI Surgical Site Infection
TEP Technical Expert Panel
TPS Total Performance Score
UMRA Unfunded Mandates Reform Act of 1995
VAD Vascular Access Device
VBP Value-Based Purchasing
I. Executive Summary
A. Purpose
This final rule updates the payment rates for home health agencies
(HHAs) for calendar year (CY) 2018, as required under section 1895(b)
of the Social Security Act (the Act). This final rule also updates the
case-mix weights under section 1895(b)(4)(A)(i) and (b)(4)(B) of the
Act for CY 2018 and implements a 0.97 percent reduction to the
national, standardized 60-day episode payment amount to account for
case-mix growth unrelated to increases in patient acuity (that is,
nominal case-mix growth) between CY 2012 and CY 2014, under the
authority of section 1895(b)(3)(B)(iv) of the Act. Additionally, this
rule finalizes changes to the Home Health Value Based Purchasing
(HHVBP) Model under the authority of section 1115A of the Act, and Home
Health Quality Reporting Program (HH QRP) requirements under the
authority of section 1895(b)(3)(B)(v) of the Act. We are not finalizing
the implementation of the Home Health Groupings Model (HHGM) in this
final rule. We received a number of comments from the public that we
would like to take into further consideration.
B. Summary of the Major Provisions
In the CY 2015 HH PPS final rule (79 FR 66072), we finalized our
proposal to recalibrate the case-mix weights every year with the most
current and complete data available at the time of rulemaking. In
section III.B. of this final rule, we are recalibrating the HH PPS
case-mix weights, using the most current cost and utilization data
available, in a budget-neutral manner. Also in section III.B. of this
final rule, as finalized in the CY 2016 HH PPS final rule (80 FR
68624), we are implementing a reduction to the national, standardized
60-day episode payment rate for CY 2018 of 0.97 percent to account for
estimated case-mix growth unrelated to increases in patient acuity
(that is, nominal case-mix growth) between CY 2012 and CY 2014. In
section III.C. of this final rule, we update the payment rates under
the HH PPS by 1 percent for CY 2018 in accordance with section 411(d)
of the Medicare Access and CHIP Reauthorization Act of 2015 (MACRA)
(Pub. L. 114-10, enacted April 16, 2015) which amended section
1895(b)(3)(B) of the Act. Additionally, section III.C. of this final
rule, updates the CY 2018 home health wage index using FY 2014 hospital
cost report data. In section III.D. of this final rule, we note that
the fixed-dollar loss ratio remains 0.55 for CY 2018 to pay up to, but
no more than, 2.5 percent of total payments as outlier payments, as
required by section 1895(b)(5)(A) of the Act.
In section IV of this final rule, we are finalizing changes to the
Home Health Value-Based Purchasing (HHVBP) Model implemented January 1,
2016. We are amending the definition of ``applicable measure'' to mean
a measure for which a competing HHA has provided a minimum of 40
completed surveys for Home Health Care Consumer Assessment of
Healthcare Providers and Systems (HHCAHPS) measures, beginning with
Performance Year (PY) 1, for purposes of receiving a performance score
for any of the HHCAHPS measures, and for PY 3 and subsequent years, we
are finalizing the removal of the Outcome and Assessment Information
Set (OASIS)-based measure, Drug Education on All Medications Provided
to Patient/Caregiver during All Episodes of Care, from the set of
applicable measures.
In section V. of this final rule, we are finalizing updates to the
Home Health Quality Reporting Program, including: The replacement of
one quality measure and the adoption of two new quality measures, data
submission requirements, exception and extension requirements, and
reconsideration and appeals procedures. We have also finalized the
removal of 235 data elements from 33 current OASIS items, effective
with all HHA assessments on or after January 1, 2019. We are not
finalizing the standardized patient assessment data elements that we
proposed to adopt for three of the five categories under section
1899B(b)(1)(B) of the Act: Cognitive Function and Mental Status;
Special Services, Treatments, and Interventions; and Impairments.
[[Page 51678]]
C. Summary of Costs and Benefits
Table 1--Summary of Costs and Transfers
------------------------------------------------------------------------
Provision description Costs Transfers
------------------------------------------------------------------------
CY 2018 HH PPS Payment Rate ................. The overall economic
Update. impact of the HH PPS
payment rate update
is an estimated -$80
million (-0.4
percent) in payments
to HHAs.
CY 2018 HHVBP Model........... ................. The overall economic
impact of the HHVBP
Model provision for
CY 2018 through 2022
is an estimated $378
million in total
savings from a
reduction in
unnecessary
hospitalizations and
SNF usage as a
result of greater
quality improvements
in the HH industry
(none of which is
attributable to the
changes finalized in
this final rule). As
for payments to
HHAs, there are no
aggregate increases
or decreases
expected to be
applied to the HHAs
competing in the
model.
CY 2019 HH QRP................ The overall .....................
economic impact
of the HH QRP
changes is a
savings to HHAs
of an estimated
$146.0 million,
beginning
January 1, 2019.
------------------------------------------------------------------------
II. Background
A. Statutory Background
The Balanced Budget Act of 1997 (BBA) (Pub. L. 105-33, enacted
August 5, 1997), significantly changed the way Medicare pays for
Medicare home health services. Section 4603 of the BBA mandated the
development of the HH PPS. Until the implementation of the HH PPS on
October 1, 2000, HHAs received payment under a retrospective
reimbursement system.
Section 4603(a) of the BBA mandated the development of a HH PPS for
all Medicare-covered home health services provided under a plan of care
(POC) that were paid on a reasonable cost basis by adding section 1895
of the Act, entitled ``Prospective Payment For Home Health Services.''
Section 1895(b)(1) of the Act requires the Secretary to establish a HH
PPS for all costs of home health services paid under Medicare. Section
1895(b)(2) of the Act requires that, in defining a prospective payment
amount, the Secretary shall consider an appropriate unit of service and
the number, type, and duration of visits provided within that unit,
potential changes in the mix of services provided within that unit and
their cost, and a general system design that provides for continued
access to quality services.
Section 1895(b)(3)(A) of the Act requires the following: (1) The
computation of a standard prospective payment amount include all costs
for HH services covered and paid for on a reasonable cost basis and
that such amounts be initially based on the most recent audited cost
report data available to the Secretary; and (2) the standardized
prospective payment amount be adjusted to account for the effects of
case-mix and wage levels among HHAs.
Section 1895(b)(3)(B) of the Act addresses the annual update to the
standard prospective payment amounts by the home health applicable
percentage increase. Section 1895(b)(4) of the Act governs the payment
computation. Sections 1895(b)(4)(A)(i) and (b)(4)(A)(ii) of the Act
require the standard prospective payment amount to be adjusted for
case-mix and geographic differences in wage levels. Section
1895(b)(4)(B) of the Act requires the establishment of an appropriate
case-mix change adjustment factor for significant variation in costs
among different units of services.
Similarly, section 1895(b)(4)(C) of the Act requires the
establishment of wage adjustment factors that reflect the relative
level of wages, and wage-related costs applicable to home health
services furnished in a geographic area compared to the applicable
national average level. Under section 1895(b)(4)(C) of the Act, the
wage-adjustment factors used by the Secretary may be the factors used
under section 1886(d)(3)(E) of the Act.
Section 1895(b)(5) of the Act gives the Secretary the option to
make additions or adjustments to the payment amount otherwise paid in
the case of outliers due to unusual variations in the type or amount of
medically necessary care. Section 3131(b)(2) of the Affordable Care Act
revised section 1895(b)(5) of the Act so that total outlier payments in
a given year would not exceed 2.5 percent of total payments projected
or estimated. The provision also made permanent a 10 percent agency-
level outlier payment cap.
In accordance with the statute, as amended by the BBA, we published
a final rule in the July 3, 2000 Federal Register (65 FR 41128) to
implement the HH PPS legislation. The July 2000 final rule established
requirements for the new HH PPS for home health services as required by
section 4603 of the BBA, as subsequently amended by section 5101 of the
Omnibus Consolidated and Emergency Supplemental Appropriations Act for
Fiscal Year 1999 (OCESAA), (Pub. L. 105-277, enacted October 21, 1998);
and by sections 302, 305, and 306 of the Medicare, Medicaid, and SCHIP
Balanced Budget Refinement Act of 1999, (BBRA) (Pub. L. 106-113,
enacted November 29, 1999). The requirements include the implementation
of a HH PPS for home health services, consolidated billing
requirements, and a number of other related changes. The HH PPS
described in that rule replaced the retrospective reasonable cost-based
system that was used by Medicare for the payment of home health
services under Part A and Part B. For a complete and full description
of the HH PPS as required by the BBA, see the July 2000 HH PPS final
rule (65 FR 41128 through 41214).
Section 5201(c) of the Deficit Reduction Act of 2005 (DRA) (Pub. L.
109-171, enacted February 8, 2006) added new section 1895(b)(3)(B)(v)
to the Act, requiring HHAs to submit data for purposes of measuring
health care quality, and links the quality data submission to the
annual applicable percentage increase. This data submission requirement
is applicable for CY 2007 and each subsequent year. If an HHA does not
submit quality data, the home health market basket percentage increase
is reduced by 2 percentage points. In the November 9, 2006 Federal
Register (71 FR 65884, 65935), we published a final rule to implement
the pay-for-reporting requirement of the DRA, which was codified at
Sec. 484.225(h) and (i) in accordance with the statute. The pay-
[[Page 51679]]
for-reporting requirement was implemented on January 1, 2007.
The Affordable Care Act made additional changes to the HH PPS. One
of the changes in section 3131 of the Affordable Care Act is the
amendment to section 421(a) of the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA) (Pub. L. 108-173,
enacted on December 8, 2003) as amended by section 5201(b) of the DRA.
Section 421(a) of the MMA, as amended by section 3131 of the Affordable
Care Act, requires that the Secretary increase, by 3 percent, the
payment amount otherwise made under section 1895 of the Act, for HH
services furnished in a rural area (as defined in section 1886(d)(2)(D)
of the Act) with respect to episodes and visits ending on or after
April 1, 2010, and before January 1, 2016.
Section 210 of the MACRA amended section 421(a) of the MMA to
extend the rural add-on for 2 more years. Section 421(a) of the MMA, as
amended by section 210 of the MACRA, requires that the Secretary
increase, by 3 percent, the payment amount otherwise made under section
1895 of the Act, for home health services provided in a rural area (as
defined in section 1886(d)(2)(D) of the Act) with respect to episodes
and visits ending on or after April 1, 2010, and before January 1,
2018. Section 411(d) of MACRA amended section 1895(b)(3)(B) of the Act
such that for home health payments for CY 2018, the market basket
percentage increase shall be 1 percent.
B. Current System for Payment of Home Health Services
Generally, Medicare currently makes payment under the HH PPS on the
basis of a national, standardized 60-day episode payment rate that is
adjusted for the applicable case-mix and wage index. The national,
standardized 60-day episode rate includes the six home health
disciplines (skilled nursing, home health aide, physical therapy,
speech-language pathology, occupational therapy, and medical social
services). Payment for non-routine supplies (NRS) is not part of the
national, standardized 60-day episode rate, but is computed by
multiplying the relative weight for a particular NRS severity level by
the NRS conversion factor. Payment for durable medical equipment
covered under the HH benefit is made outside the HH PPS payment system.
To adjust for case-mix, the HH PPS uses a 153-category case-mix
classification system to assign patients to a home health resource
group (HHRG). The clinical severity level, functional severity level,
and service utilization are computed from responses to selected data
elements in the OASIS assessment instrument and are used to place the
patient in a particular HHRG. Each HHRG has an associated case-mix
weight which is used in calculating the payment for an episode. Therapy
service use is measured by the number of therapy visits provided during
the episode and can be categorized into nine visit level categories (or
thresholds): 0 to 5; 6; 7 to 9; 10; 11 to 13; 14 to 15; 16 to 17; 18 to
19; and 20 or more visits.
For episodes with four or fewer visits, Medicare pays national per-
visit rates based on the discipline(s) providing the services. An
episode consisting of four or fewer visits within a 60-day period
receives what is referred to as a low-utilization payment adjustment
(LUPA). Medicare also adjusts the national standardized 60-day episode
payment rate for certain intervening events that are subject to a
partial episode payment adjustment (PEP adjustment). For certain cases
that exceed a specific cost threshold, an outlier adjustment may also
be available.
C. Updates to the Home Health Prospective Payment System
As required by section 1895(b)(3)(B) of the Act, we have
historically updated the HH PPS rates annually in the Federal Register.
The August 29, 2007 final rule with comment period set forth an update
to the 60-day national episode rates and the national per-visit rates
under the HH PPS for CY 2008. The CY 2008 HH PPS final rule included an
analysis performed on CY 2005 home health claims data, which indicated
a 12.78 percent increase in the observed case-mix since 2000. Case-mix
represents the variations in conditions of the patient population
served by the HHAs. Subsequently, a more detailed analysis was
performed on the 2005 case-mix data to evaluate if any portion of the
12.78 percent increase was associated with a change in the actual
clinical condition of home health patients. We identified 8.03 percent
of the total case-mix change as real, and therefore, decreased the
12.78 percent of total case-mix change by 8.03 percent to get a final
nominal case-mix increase measure of 11.75 percent (0.1278 * (1-0.0803)
= 0.1175).
To account for the changes in case-mix that were not related to an
underlying change in patient health status, we implemented a reduction,
over 4 years, to the national, standardized 60-day episode payment
rates. That reduction was to be 2.75 percent per year for 3 years
beginning in CY 2008 and 2.71 percent for the fourth year in CY 2011.
In the CY 2011 HH PPS final rule (76 FR 68532), we updated our analyses
of case-mix change and finalized a reduction of 3.79 percent, instead
of 2.71 percent, for CY 2011 and deferred finalizing a payment
reduction for CY 2012 until further study of the case-mix change data
and methodology was completed.
In the CY 2012 HH PPS final rule (76 FR 68526), we updated the 60-
day national episode rates and the national per-visit rates. In
addition, as discussed in the CY 2012 HH PPS final rule (76 FR 68528),
our analysis indicated that there was a 22.59 percent increase in
overall case-mix from 2000 to 2009 and that only 15.76 percent of that
overall observed case-mix percentage increase was due to real case-mix
change. As a result of our analysis, we identified a 19.03 percent
nominal increase in case-mix. At that time, to fully account for the
19.03 percent nominal case-mix growth identified from 2000 to 2009, we
finalized a 3.79 percent payment reduction in CY 2012 and a 1.32
percent payment reduction for CY 2013.
In the CY 2013 HH PPS final rule (77 FR 67078), we implemented the
1.32 percent reduction to the payment rates for CY 2013 finalized the
previous year, to account for nominal case-mix growth from 2000 through
2010. When taking into account the total measure of case-mix change
(23.90 percent) and the 15.97 percent of total case-mix change
estimated as real from 2000 to 2010, we obtained a final nominal case-
mix change measure of 20.08 percent from 2000 to 2010 (0.2390 * (1-
0.1597) = 0.2008). To fully account for the remainder of the 20.08
percent increase in nominal case-mix beyond that which was accounted
for in previous payment reductions, we estimated that the percentage
reduction to the national, standardized 60-day episode rates for
nominal case-mix change would be 2.18 percent. Although we considered
proposing a 2.18 percent reduction to account for the remaining
increase in measured nominal case-mix, we finalized the 1.32 percent
payment reduction to the national, standardized 60-day episode rates in
the CY 2012 HH PPS final rule (76 FR 68532).
Section 3131(a) of the Affordable Care Act requires that, beginning
in CY 2014, we apply an adjustment to the national, standardized 60-day
episode rate and other amounts that reflect factors such as changes in
the number of visits in an episode, the mix of services in an episode,
the level of intensity of services in an episode, the average cost of
providing care per episode, and other relevant factors. Additionally,
we must phase in any adjustment over a 4-year
[[Page 51680]]
period in equal increments, not to exceed 3.5 percent of the amount (or
amounts) as of the date of enactment of the Affordable Care Act, and
fully implement the rebasing adjustments by CY 2017. The statute
specifies that the maximum rebasing adjustment is to be no more than
3.5 percent per year of the CY 2010 rates. Therefore, in the CY 2014 HH
PPS final rule (78 FR 72256) for each year, CY 2014 through CY 2017, we
finalized a fixed-dollar reduction to the national, standardized 60-day
episode payment rate of $80.95 per year, increases to the national per-
visit payment rates per year, and a decrease to the NRS conversion
factor of 2.82 percent per year. We also finalized three separate LUPA
add-on factors for skilled nursing, physical therapy, and speech-
language pathology and removed 170 diagnosis codes from assignment to
diagnosis groups in the HH PPS Grouper. In the CY 2015 HH PPS final
rule (79 FR 66032), we implemented the second year of the 4-year phase-
in of the rebasing adjustments to the HH PPS payment rates and made
changes to the HH PPS case-mix weights. In addition, we simplified the
face-to-face encounter regulatory requirements and the therapy
reassessment timeframes.
In the CY 2016 HH PPS final rule (80 FR 68624), we implemented the
third year of the 4-year phase-in of the rebasing adjustments to the
national, standardized 60-day episode payment amount, the national per-
visit rates and the NRS conversion factor (as outlined previously). In
the CY 2016 HH PPS final rule, we also recalibrated the HH PPS case-mix
weights, using the most current cost and utilization data available, in
a budget-neutral manner and finalized reductions to the national,
standardized 60-day episode payment rate in CY 2016, CY 2017, and CY
2018 of 0.97 percent in each year to account for estimated case-mix
growth unrelated to increases in patient acuity (that is, nominal case-
mix growth) between CY 2012 and CY 2014. Finally, section 421(a) of the
MMA, as amended by section 210 of the MACRA, extended the payment
increase of 3 percent for HH services provided in rural areas (as
defined in section 1886(d)(2)(D) of the Act) to episodes or visits
ending before January 1, 2018.
In the CY 2017 HH PPS final rule (81 FR 76702), we implemented the
last year of the 4-year phase-in of the rebasing adjustments to the
national, standardized 60-day episode payment amount, the national per-
visit rates and the NRS conversion factor (as outlined previously). We
also finalized changes to the methodology used to calculate outlier
payments under the authority of section 1895(b)(5) of the Act. Lastly,
in accordance with section 1834(s) of the Act, as added by section
504(a) of the Consolidated Appropriations Act, 2016 (Pub. L. 114-113,
enacted December 18, 2015), we implemented changes in payment for
furnishing Negative Pressure Wound Therapy (NPWT) using a disposable
device for patients under a home health plan of care for which payment
would otherwise be made under section 1895(b) of the Act.
D. Report to Congress: Home Health Study on Access to Care for
Vulnerable Patient Populations and Subsequent Research and Analyses
Section 3131(d) of the Affordable Care Act required CMS to conduct
a study on home health agency costs involved with providing ongoing
access to care to low-income Medicare beneficiaries or beneficiaries in
medically underserved areas, and in treating beneficiaries with varying
levels of severity of illness and submit a report to Congress. As
discussed in the CY 2016 HH PPS proposed rule (80 FR 39840) and the CY
2017 HH PPS proposed rule (81 FR 43744), the findings from the Report
to Congress on the ``Medicare Home Health Study: An Investigation on
Access to Care and Payment for Vulnerable Patient Populations,'' found
that payment accuracy could be improved under the current payment
system, particularly for patients with certain clinical characteristics
requiring more nursing care than therapy.\1\
---------------------------------------------------------------------------
\1\ The Report to Congress can be found in its entirety at
https://www.cms.gov/Medicare/Medicare-Fee-for-ServicePayment/HomeHealthPPS/Downloads/HH-Report-to-Congress.pdf.
---------------------------------------------------------------------------
The research for the Report to Congress, released in December 2014,
consisted of extensive analysis of both survey and administrative data.
The CMS-developed surveys were given to physicians who referred
vulnerable patient populations to Medicare home health and to Medicare-
certified HHAs.\2\ The response rates were 72 percent and 59 percent
for the HHA and physician surveys, respectively. The results of the
survey revealed that over 80 percent of respondent HHAs and over 90
percent of respondent physicians reported that access to home health
care for Medicare fee-for-service beneficiaries in their local area was
excellent or good. When survey respondents reported access issues,
specifically their inability to place or admit Medicare fee-for-service
patients into home health, the most common reason reported (64 percent
of respondent HHAs surveyed) was that the patients did not qualify for
the Medicare home health benefit. HHAs and physicians also cited family
or caregiver issues as an important contributing factor in the
inability to admit or place patients. Only 17.2 percent of HHAs and
16.7 percent of physicians reported insufficient payment as an
important contributing factor in the inability to admit or place
patients. The results of the CMS-conducted surveys suggested that CMS'
ability to improve access for certain vulnerable patient populations
through payment policy may be limited. However, we are able to revise
the case-mix system to minimize differences in payment that could
potentially be serving as a barrier to receiving care. In the near
future, we intend to better align payment with resource use so that it
reduces HHAs' financial incentives to select certain patients over
others.
---------------------------------------------------------------------------
\2\ For the purposes of the surveys, ``vulnerable patient
populations'' were defined as beneficiaries who were either eligible
for the Part D low-income subsidy (LIS) 27 or residing in a health
professional shortage area (HPSA).
---------------------------------------------------------------------------
We also performed an analysis of Medicare administrative data (CY
2010 Medicare claims and cost report data) and calculated margins for
episodes of care. This was done because margin differences associated
with patient clinical and social characteristics can indicate whether
financial incentives exist in the current HH PPS to provide home health
care for certain types of patients over others. Lower margins, if
systematically associated with care for vulnerable patient populations,
may indicate financial disincentives for HHAs to admit these patients,
potentially creating access to care issues. The findings from the data
analysis found that certain patient characteristics appear to be
strongly associated with margin levels, and thus may create financial
incentives to select certain patients over others. Margins were
estimated to be lower for patients who required parenteral nutrition,
who had traumatic wounds or ulcers, or required substantial assistance
in bathing. For example, in CY 2010, episodes for patients with
parenteral nutrition were, on average, associated with a $178.53 lower
margin than episodes for patients without parenteral nutrition. Given
that these variables are already included in the HH PPS case-mix
system, the results indicated that modifications to the way the current
case-mix system accounts for resource use differences may be needed to
mitigate any financial incentives to select certain patients over
others. Margins were also lower for beneficiaries who were admitted
after acute or post-acute stays or who had certain poorly-controlled
clinical
[[Page 51681]]
conditions, such as poorly controlled pulmonary disorders, indicating
that accounting for additional patient characteristic variables in the
HH PPS case-mix system may also reduce financial incentives to select
certain types of patients over others. More information on the results
from the home health study required by section 3131(d) of the
Affordable Care Act can be found in the Report to Congress on the
``Medicare Home Health Study: An Investigation on Access to Care and
Payment for Vulnerable Patient Populations'' available at https://www.cms.gov/center/provider-Type/home-Health-Agency-HHA-Center.html.
Section 3131(d)(5) of the Affordable Care Act authorized the
Secretary to determine whether it would be appropriate to conduct a
Medicare demonstration project based on the result of the home health
study. If the Secretary determined it was appropriate to conduct the
demonstration project under this subsection, the Secretary was to
conduct the project for a 4-year period beginning not later than
January 1, 2015. We did not determine that it was appropriate to
conduct a demonstration project based on the findings from the home
health study. Rather, the findings from the home health study suggested
that follow-on work should be conducted to better align payments with
costs under the authority of section 1895 of the Act.
In addition to the findings from the Report to Congress on the
``Medicare Home Health Study: An Investigation on Access to Care and
Payment for Vulnerable Patient Populations,'' concerns have also been
raised about the use of therapy thresholds in the current payment
system. Under the current payment system, HHAs receive higher payments
for providing more therapy visits once certain thresholds are reached.
As a result, the average number of therapy visits per 60-day episode of
care have increased since the implementation of the HH PPS, while the
number of skilled nursing and home health aide visits have decreased
over the same time period (82 FR 35280 (Figure 3)). A study examining
an option of using predicted, rather than actual, therapy visits in the
home health found that in 2013, 58 percent of home health episodes
included some therapy services, and these episodes accounted for 72
percent of all Medicare home health payments.\3\ Figure 1, from that
study, demonstrates that the percentage of episodes, and the average
episode payment by the number of therapy visits for episodes with at
least one therapy visit in 2013 increased sharply in therapy provision
just over payment thresholds at 6, 7, and 16. According to the study,
the presence of sharp increases in the percentage of episodes just
above payment thresholds suggests a response to financial incentives in
the home health payment system. Similarly, between 2008 and 2013,
MedPAC reported a 26 percent increase in the number of episodes with at
least 6 therapy visits, compared with a 1 percent increase in the
number of episodes with 5 or fewer therapy visits.\4\ CMS analysis
demonstrates that the average share of therapy visits across all 60-day
episodes of care increased from 9 percent of all visits in 1997, prior
to the implementation of the HH PPS (see 64 FR 58151), to 39 percent of
all visits in 2015 (82 FR 35277 through 35278 (Table 2)).
---------------------------------------------------------------------------
\3\ Fout B, Plotzke M, Christian T. (2016). Using Predicted
Therapy Visits in the Medicare Home Health Prospective Payment
System. Home Health Care Management & Practice, 29(2), 81-90. https://journals.sagepub.com/doi/abs/10.1177/1084822316678384.
\4\ Medicare Payment Advisory Commission (MedPAC). ``Home Health
Care Services.'' Report to Congress: Medicare Payment Policy.
Washington, DC, March 2015. P. 223. Accessed on March 28, 2017 at:
https://www.medpac.gov/docs/default-source/reports/mar2015_entirereport_revised.pdf?sfvrsn=0.
---------------------------------------------------------------------------
[[Page 51682]]
[GRAPHIC] [TIFF OMITTED] TR07NO17.000
Figure 1 suggests that HHAs may be responding to financial
incentives in the home health payment system when making care plan
decisions. Additionally, an investigation into the therapy practices of
the four largest publically-traded home health companies, conducted by
the Senate Committee on Finance in 2010, found that three out of the
four companies investigated ``encouraged therapists to target the most
profitable number of therapy visits, even when patient need alone may
not have justified such patterns''.\5\ The Senate Committee on Finance
investigation also highlighted the abrupt and dramatic responses the
home health industry has taken to maximize reimbursement under the
therapy threshold models (both the original 10-visit threshold model
and under the revised thresholds implemented in the CY 2008 HH PPS
final rule (72 FR 49762)). The report noted that, under the HH PPS,
HHAs have broad discretion over the number of therapy visits to provide
patients, and therefore, have control of the single-largest variable in
determining reimbursement and overall margins. The report recommended
that CMS closely examine a future payment approach that focuses on
patient well-being and health characteristics, rather than the
numerical utilization measures.
---------------------------------------------------------------------------
\5\ Committee on Finance, United States Senate. Staff Report on
Home Health and the Medicare Therapy Threshold. Washington, DC,
2011. Accessed on March 28, 2017 at https://www.finance.senate.gov/imo/media/doc/Home_Health_Report_Final4.pdf.
---------------------------------------------------------------------------
MedPAC also continues to recommend the removal of the therapy
thresholds used for determining payment from the HH PPS, as it believes
that such thresholds run counter to the goals of a prospective payment
system, create financial incentives that detract from a focus on
patient characteristics and care needs when agencies are setting plans
of care for their patients, and incentivize unnecessary therapy
utilization. For the average HHA, according to MedPAC, the increase in
payment for therapy visits rises faster than costs, resulting in
financial incentives for HHAs to overprovide therapy services.\6\ HHAs
that provide more therapy episodes tend to be more profitable and this
higher profitability and rapid growth in the number of therapy episodes
suggest that financial incentives are causing agencies to favor therapy
services when possible.\7\ Eliminating therapy as a payment factor will
base home health payment solely on patient characteristics, which is a
more patient-focused approach to payment, as recommended by both MedPAC
and previously by the Senate Committee on Finance.
---------------------------------------------------------------------------
\6\ Medicare Payment Advisory Commission (MedPAC). ``Home Health
Services.'' Report to Congress: Medicare Payment Policy. Washington,
DC, March 2011. P. 182-183. Accessed on March 28, 2017 at https://www.medpac.gov/docs/default-source/reports/Mar11_Ch08.pdf?sfvrsn=0.
\7\ Medicare Payment Advisory Commission (MedPAC). ``Home Health
Care Services.'' Report to Congress: Medicare Payment Policy.
Washington, DC, March 2017. P. 243-244. Accessed on March 28, 2017
at https://www.medpac.gov/docs/default-source/reports/mar17_medpac_ch9.pdf?sfvrsn=0.
---------------------------------------------------------------------------
After considering the findings from the Report to Congress and
recommendations from MedPAC and the Senate Committee on Finance, CMS,
along with our contractor, conducted additional research on ways to
improve the payment accuracy under the current payment system.
Exploring all options and different models ultimately led us to further
develop the Home Health Groupings Model (HHGM). As discussed in the CY
2018 HH PPS proposed rule (82 FR 35294), we shared
[[Page 51683]]
the analysis and development of the HHGM with both internal and
external stakeholders via technical expert panels, clinical workgroups,
special open door forums, in the CY 2016 HH PPS proposed rule (80 FR
39840) and the CY 2017 HH PPS proposed rule (81 FR 43744), in a
detailed technical report posted on the CMS Web site in December 2016
(followed by additional technical and clinical expert panels) and a
National Provider Call in January 2017. The HHGM uses 30-day periods,
rather than 60-day episodes, and relies more heavily on clinical
characteristics and other patient information (for example, principal
diagnosis, functional level, comorbid conditions, admission source, and
timing) to place patients into meaningful payment categories, rather
than the current therapy-driven system, which are the major differences
between the current system and the HHGM.
III. Provisions of the Proposed Rule: Payment Under the Home Health
Prospective Payment System (HH PPS) and Responses to Comments
In the July 28, 2017 Federal Register (82 FR 35270 through 35393),
we published the proposed rule titled ``Medicare and Medicaid Programs;
CY 2018 Home Health Prospective Payment System Rate Update and Proposed
CY 2019 Case-Mix Adjustment Methodology Refinements; Home Health Value-
Based Purchasing Model; and Home Health Quality Reporting
Requirements''. We received approximately 1,346 timely comments from
the public, including comments from home health agencies, national and
state provider associations, patient and other advocacy organizations,
nurses, and physical therapists. In the following sections, we
summarize the proposed provisions and the public comments, and provide
the responses to comments.
A. Monitoring for Potential Impacts--Affordable Care Act Rebasing
Adjustments
In the CY 2018 HH PPS proposed rule (82 FR 35277), we provided a
summary of analysis on fiscal year (FY) 2015 HHA cost report data and
how such data, if used, would impact our estimate of the percentage
difference between Medicare payments and HHA costs used to calculate
the Affordable Care Act rebasing adjustments. In addition, we presented
information on Medicare home health utilization statistics and trends
that included HHA claims data through CY 2016. We will continue
monitoring the impacts due to the rebasing adjustments and other policy
changes and will provide the industry with periodic updates on our
analysis in rulemaking and announcements on the HHA Center Web page at
https://www.cms.gov/Center/Provider-Type/Home-Health-Agency-HHA-
Center.html.
The following is a summary of the comments received on the analysis
of HHA cost report and utilization data and our responses.
Comment: A commenter noted that it may come as no surprise that
payments exceed costs by 21 percent, given that Medicare payment for
home health is statutorily required to be based on a prospective
payment system and the industry is now 90 percent for-profit, with
incentives to admit only the most profitable cases. The commenter went
on to state that home health payments from Medicare Advantage (MA)
plans are inadequate and that HHAs subsidize low payments from MA plans
with payments for fee-for-service patients. The commenter further noted
that the number of patients coming into home health care from the
community (rather than following an acute or post-acute care stay) has
risen in response to deliberate Medicare and public health effort to
keep patients out of the hospital. Similar comments from MedPAC stated
that CMS's review of utilization is consistent with the Commission's
findings on access to care, and the analysis of the cost and
utilization data in the proposed rule underscores the Commission's
long-standing concern that the Patient Protection and Affordable Care
Act (PPACA) rebasing provision would not adequately reduce payments.
Response: We thank the commenters for their feedback on the HHA
cost and utilization data presented in the proposed rule. We will
continue monitoring the impacts due to the rebasing adjustments and
other policy changes and will provide the industry with periodic
updates on our analysis in rulemaking or announcements on the HHA
Center Web page at: https://www.cms.gov/Center/Provider-Type/Home-
Health-Agency-HHA-Center.html.
Comment: A commenter questioned whether CMS did any trimming to the
cost report data used to populate Table 2 in the CY 2018 HH PPS
proposed rule and whether NRS costs were excluded from this
calculation.
Response: As we noted in the CY 2018 HH PPS proposed rule (82 FR
35277), to determine the 2015 average cost per visit per discipline, we
applied the same trimming methodology outlined in the CY 2014 HH PPS
proposed rule (78 FR 40284) and weighted the costs per visit from the
2015 cost reports by size, facility type, and urban/rural location so
the costs per visit were nationally representative according to 2015
claims data. The 2015 average number of visits was taken from 2015
claims data (82 FR 35277). Because CMS currently pays for NRS using a
separate conversion factor, NRS costs were not included in Table 2 as
the national, standardized 60-day episode payment amount only reflects
the cost of care related to skilled nursing, physical therapy,
occupational therapy, speech-language pathology, home health aide, and
medical social services. The payment for NRS is calculated through the
NRS conversion factor, multiplied by the weights for the six severity
levels.
B. CY 2018 HH PPS Case-Mix Weights
In the CY 2015 HH PPS final rule (79 FR 66072), we finalized a
policy to annually recalibrate the HH PPS case-mix weights--adjusting
the weights relative to one another--using the most current, complete
data available. To recalibrate the HH PPS case-mix weights for CY 2018,
we will use the same methodology finalized in the CY 2008 HH PPS final
rule (72 FR 49762), the CY 2012 HH PPS final rule (76 FR 68526), and
the CY 2015 HH PPS final rule (79 FR 66032). Annual recalibration of
the HH PPS case-mix weights ensures that the case-mix weights reflect,
as accurately as possible, current home health resource use and changes
in utilization patterns.
To generate the CY 2018 HH PPS case-mix weights, we used CY 2016
home health claims data (as of August 17, 2017) with linked OASIS data.
These data are the most current and complete data available at this
time. We noted in the proposed rule that we would use CY 2016 home
health claims data (as of June 30, 2017 or later) with linked OASIS
data to generate the CY 2018 HH PPS case-mix weights for this final
rule. The process we used to calculate the HH PPS case-mix weights is
outlined in this section.
Step 1: Re-estimate the four-equation model to determine the
clinical and functional points for an episode using wage-weighted
minutes of care as our dependent variable for resource use. The wage-
weighted minutes of care are determined using the CY 2015 Bureau of
Labor Statistics national hourly wage plus fringe rates for the six
home health disciplines and the minutes per visit from the claim. The
points for each of the variables for each leg of the model, updated
with CY 2016 home health claims data, are shown in Table 2. The points
for the clinical variables are added together to determine an episode's
clinical score. The points for the functional variables are added
[[Page 51684]]
together to determine an episode's functional score.
Table 2--Case-Mix Adjustment Variables and Scores
----------------------------------------------------------------------------------------------------------------
----------------------------------------------------------------------------------------------------------------
Episode number within 1 or 2 1 or 2 3+ 3+
sequence of adjacent
episodes.
Therapy visits........... 0-13 14+ 0-13 14+
EQUATION:................ 1 2 3 4
----------------------------------------------------------------------------------------------------------------
CLINICAL DIMENSION
----------------------------------------------------------------------------------------------------------------
1.................... Primary or Other .............. .............. .............. ..............
Diagnosis = Blindness/
Low Vision.
2.................... Primary or Other .............. 1 .............. ..............
Diagnosis = Blood
disorders.
3.................... Primary or Other .............. 4 .............. 4
Diagnosis = Cancer,
selected benign
neoplasms.
4.................... Primary Diagnosis = .............. 3 .............. ..............
Diabetes.
5.................... Other Diagnosis = 1 .............. .............. ..............
Diabetes.
6.................... Primary or Other 2 16 1 10
Diagnosis = Dysphagia
AND Primary or Other
Diagnosis = Neuro 3--
Stroke.
7.................... Primary or Other 1 5 .............. 9
Diagnosis = Dysphagia
AND M1030 (Therapy at
home) = 3 (Enteral).
8.................... Primary or Other .............. .............. .............. 2
Diagnosis =
Gastrointestinal
disorders.
9.................... Primary or Other .............. 7 .............. ..............
Diagnosis =
Gastrointestinal
disorders AND M1630
(ostomy)= 1 or 2.
10................... Primary or Other .............. .............. .............. ..............
Diagnosis =
Gastrointestinal
disorders AND Primary or
Other Diagnosis = Neuro
1--Brain disorders and
paralysis, OR Neuro 2--
Peripheral neurological
disorders, OR Neuro 3--
Stroke, OR Neuro 4--
Multiple Sclerosis.
11................... Primary or Other 1 3 .............. 2
Diagnosis = Heart
Disease OR Hypertension.
12................... Primary Diagnosis = Neuro 3 9 6 9
1--Brain disorders and
paralysis.
13................... Primary or Other .............. 4 .............. 4
Diagnosis = Neuro 1--
Brain disorders and
paralysis AND M1840
(Toilet transfer) = 2 or
more.
14................... Primary or Other 2 4 2 4
Diagnosis = Neuro 1--
Brain disorders and
paralysis OR Neuro 2--
Peripheral neurological
disorders AND M1810 or
M1820 (Dressing upper or
lower body) = 1, 2, or 3.
15................... Primary or Other 3 9 2 4
Diagnosis = Neuro 3--
Stroke.
16................... Primary or Other .............. 2 .............. ..............
Diagnosis = Neuro 3--
Stroke AND M1810 or
M1820 (Dressing upper or
lower body) = 1, 2, or 3.
17................... Primary or Other .............. .............. .............. ..............
Diagnosis = Neuro 3--
Stroke AND M1860
(Ambulation) = 4 or more.
18................... Primary or Other 3 7 5 11
Diagnosis = Neuro 4--
Multiple Sclerosis AND
AT LEAST ONE OF THE
FOLLOWING: M1830
(Bathing) = 2 or more OR
M1840 (Toilet transfer)
= 2 or more OR M1850
(Transferring) = 2 or
more OR M1860
(Ambulation) = 4 or more.
19................... Primary or Other 7 1 7 ..............
Diagnosis = Ortho 1--Leg
Disorders or Gait
Disorders AND M1324
(most problematic
pressure ulcer stage) =
1, 2, 3 or 4.
20................... Primary or Other 3 .............. 3 7
Diagnosis = Ortho 1--Leg
OR Ortho 2--Other
orthopedic disorders AND
M1030 (Therapy at home)
= 1 (IV/Infusion) or 2
(Parenteral).
21................... Primary or Other .............. .............. .............. ..............
Diagnosis = Psych 1--
Affective and other
psychoses, depression.
22................... Primary or Other .............. .............. .............. ..............
Diagnosis = Psych 2--
Degenerative and other
organic psychiatric
disorders.
23................... Primary or Other .............. 2 .............. 1
Diagnosis = Pulmonary
disorders.
24................... Primary or Other .............. .............. .............. ..............
Diagnosis = Pulmonary
disorders AND M1860
(Ambulation) = 1 or more.
25................... Primary Diagnosis = Skin 3 17 6 17
1--Traumatic wounds,
burns, and post-
operative complications.
26................... Other Diagnosis = Skin 1-- 6 14 7 14
Traumatic wounds, burns,
post-operative
complications.
27................... Primary or Other 2 .............. .............. ..............
Diagnosis = Skin 1--
Traumatic wounds, burns,
and post-operative
complications OR Skin 2--
Ulcers and other skin
conditions AND M1030
(Therapy at home) = 1
(IV/Infusion) or 2
(Parenteral).
28................... Primary or Other 2 16 8 18
Diagnosis = Skin 2--
Ulcers and other skin
conditions.
29................... Primary or Other 2 17 .............. 17
Diagnosis = Tracheostomy.
30................... Primary or Other .............. 17 .............. 12
Diagnosis = Urostomy/
Cystostomy.
31................... M1030 (Therapy at home) = .............. 15 5 15
1 (IV/Infusion) or 2
(Parenteral).
32................... M1030 (Therapy at home) = .............. 16 .............. 6
3 (Enteral).
33................... M1200 (Vision) = 1 or .............. .............. .............. ..............
more.
34................... M1242 (Pain)= 3 or 4..... 3 .............. 2 ..............
35................... M1311 = Two or more 4 6 4 6
pressure ulcers at stage
3 or 4.
36................... M1324 (Most problematic 4 19 7 17
pressure ulcer stage) =
1 or 2.
37................... M1324 (Most problematic 9 31 10 25
pressure ulcer stage)= 3
or 4.
38................... M1334 (Stasis ulcer 4 13 8 13
status) = 2.
39................... M1334 (Stasis ulcer 7 17 9 17
status) = 3.
40................... M1342 (Surgical wound 2 7 6 13
status) = 2.
41................... M1342 (Surgical wound .............. 6 5 10
status) = 3.
42................... M1400 (Dyspnea) = 2, 3, 1 1 .............. ..............
or 4.
43................... M1620 (Bowel .............. 3 .............. 2
Incontinence) = 2 to 5.
44................... M1630 (Ostomy) = 1 or 2.. 4 11 2 8
45................... M2030 (Injectable Drug .............. .............. .............. ..............
Use) = 0, 1, 2, or 3.
----------------------------------------------------------------------------------------------------------------
FUNCTIONAL DIMENSION
----------------------------------------------------------------------------------------------------------------
46................... M1810 or M1820 (Dressing 1 .............. .............. ..............
upper or lower body) =
1, 2, or 3.
47................... M1830 (Bathing) = 2 or 6 5 6 2
more.
48................... M1840 (Toilet .............. 1 .............. ..............
transferring) = 2 or
more.
[[Page 51685]]
49................... M1850 (Transferring) = 2 3 1 2 .
or more.
50................... M1860 (Ambulation) = 1, 2 7 .............. 4 ..............
or 3.
51................... M1860 (Ambulation) = 4 or 8 9 7 7
more.
----------------------------------------------------------------------------------------------------------------
Source: CY 2016 Medicare claims data for episodes ending on or before December 31, 2016 (as of August 17, 2017)
for which we had a linked OASIS assessment. LUPA episodes, outlier episodes, and episodes with PEP adjustments
were excluded.
Note(s): Points are additive; however, points may not be given for the same line item in the table more than
once. Please see Medicare Home Health Diagnosis Coding guidance at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/HomeHealthPPS/coding_billing.html for definitions of primary and secondary diagnoses.
In updating the four-equation model for CY 2018, using 2016 home
health claims data (the last update to the four-equation model for CY
2017 used CY 2015 home health claims data), there were few changes to
the point values for the variables in the four-equation model. These
relatively minor changes reflect the change in the relationship between
the grouper variables and resource use between CY 2015 and CY 2016. The
CY 2018 four-equation model resulted in 120 point-giving variables
being used in the model (as compared to the 124 variables for the CY
2017 recalibration). There were 8 variables that were added to the
model and 12 variables that were dropped from the model due to the
absence of additional resources associated with the variable. Of the
variables that were in both the four-equation model for CY 2017 and the
four-equation model for CY 2018, the points for 14 variables increased
in the CY 2018 four-equation model and the points for 48 variables
decreased in the CY 2018 4-equation model. There were 50 variables with
the same point values.
Step 2: Redefining the clinical and functional thresholds so they
are reflective of the new points associated with the CY 2018 four-
equation model. After estimating the points for each of the variables
and summing the clinical and functional points for each episode, we
look at the distribution of the clinical score and functional score,
breaking the episodes into different steps. The categorizations for the
steps are as follows:
Step 1: First and second episodes, 0-13 therapy visits.
Step 2.1: First and second episodes, 14-19 therapy visits.
Step 2.2: Third episodes and beyond, 14-19 therapy visits.
Step 3: Third episodes and beyond, 0-13 therapy visits.
Step 4: Episodes with 20+ therapy visits
Then, we divide the distribution of the clinical score for episodes
within a step such that a third of episodes are classified as low
clinical score, a third of episodes are classified as medium clinical
score, and a third of episodes are classified as high clinical score.
The same approach is then done looking at the functional score. It was
not always possible to evenly divide the episodes within each step into
thirds due to many episodes being clustered around one particular
score.\8\ Also, we looked at the average resource use associated with
each clinical and functional score and used that as a guide for setting
our thresholds. We grouped scores with similar average resource use
within the same level (even if it meant that more or less than a third
of episodes were placed within a level). The new thresholds, based off
the CY 2018 four-equation model points are shown in Table 3.
---------------------------------------------------------------------------
\8\ For Step 1, 45.3 percent of episodes were in the medium
functional level (All with score 14).
For Step 2.1, 87.3 percent of episodes were in the low
functional level (Most with scores 5 to 7).
For Step 2.2, 81.9 percent of episodes were in the low
functional level (Most with score 2).
For Step 3, 46.3 percent of episodes were in the medium
functional level (Most with score 10).
For Step 4, 48.7 percent of episodes were in the medium
functional level (Most with score 5 or 6).
Table 3--CY 2018 Clinical and Functional Thresholds
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
1st and 2nd episodes 3rd+ episodes All episodes
----------------------------------------------------------------------------------------------------------------------------------------
0 to 13 therapy visits 14 to 19 therapy visits 0 to 13 therapy visits 14 to 19 therapy visits 20+ therapy visits
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Grouping Step 1 2......................... 3........................ 4........................ 5
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Equations used to calculate points (see Table 1) 1 2......................... 3........................ 4........................ (2&4)
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Dimension Severity Level
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Clinical.......................... C1................. 0 to 1.................... 0 to 1.................... 0 to 1................... 0 to 1................... 0 to 3
C2................. 2 to 3.................... 2 to 7.................... 2........................ 2 to 9................... 4 to 16
C3................. 4+........................ 8+........................ 3+....................... 10+...................... 17+
Functional........................ F1................. 0 to 13................... 0 to 7.................... 0 to 6................... 0 to 2................... 0 to 2
F2................. 14........................ 8 to 15................... 7 to 10.................. 3 to 7................... 3 to 6
F3................. 15+....................... 16+....................... 11+...................... 8+....................... 7+
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Step 3: Once the clinical and functional thresholds are determined
and each episode is assigned a clinical and functional level, the
payment regression is estimated with an episode's wage-weighted minutes
of care as the dependent variable. Independent variables in the model
are indicators for the step of the episode as well as the clinical and
functional levels within each step of the episode. Like the four-
equation model, the payment regression model is also estimated with
robust standard errors that are clustered at the beneficiary level.
Table 4 shows the regression coefficients for the variables in the
payment regression model updated with CY 2016 home health claims data.
The R-squared value for the payment regression model is
[[Page 51686]]
0.5095 (an increase from 0.4919 for the CY 2017 recalibration).
Table 4--Payment Regression Model
------------------------------------------------------------------------
Payment regression
from
4[dash]equation
model for CY 2018
------------------------------------------------------------------------
Step 1, Clinical Score Medium....................... $24.58
Step 1, Clinical Score High......................... 54.24
Step 1, Functional Score Medium..................... 72.76
Step 1, Functional Score High....................... 107.48
Step 2.1, Clinical Score Medium..................... 48.81
Step 2.1, Clinical Score High....................... 135.99
Step 2.1, Functional Score Medium................... 31.51
Step 2.1, Functional Score High..................... 57.73
Step 2.2, Clinical Score Medium..................... 39.37
Step 2.2, Clinical Score High....................... 194.18
Step 2.2, Functional Score Medium................... 21.53
Step 2.2, Functional Score High..................... 56.25
Step 3, Clinical Score Medium....................... 17.07
Step 3, Clinical Score High......................... 95.93
Step 3, Functional Score Medium..................... 59.15
Step 3, Functional Score High....................... 90.40
Step 4, Clinical Score Medium....................... 80.09
Step 4, Clinical Score High......................... 263.75
Step 4, Functional Score Medium..................... 27.97
Step 4, Functional Score High....................... 62.20
Step 2.1, 1st and 2nd Episodes, 14 to 19 Therapy 512.27
Visits.............................................
Step 2.2, 3rd+ Episodes, 14 to 19 Therapy Visits.... 523.60
Step 3, 3rd+ Episodes, 0-13 Therapy Visits.......... -72.22
Step 4, All Episodes, 20+ Therapy Visits............ 907.99
Intercept........................................... 389.35
------------------------------------------------------------------------
Source: CY 2016 Medicare claims data for episodes ending on or before
December 31, 2016 (as of August 17, 2017) for which we had a linked
OASIS assessment.
Step 4: We use the coefficients from the payment regression model
to predict each episode's wage-weighted minutes of care (resource use).
We then divide these predicted values by the mean of the dependent
variable (that is, the average wage-weighted minutes of care across all
episodes used in the payment regression). This division constructs the
weight for each episode, which is simply the ratio of the episode's
predicted wage-weighted minutes of care divided by the average wage-
weighted minutes of care in the sample. Each episode is then aggregated
into one of the 153 home health resource groups (HHRGs) and the ``raw''
weight for each HHRG was calculated as the average of the episode
weights within the HHRG.
Step 5: The raw weights associated with 0 to 5 therapy visits are
then increased by 3.75 percent, the weights associated with 14 to 15
therapy visits are decreased by 2.5 percent, and the weights associated
with 20+ therapy visits are decreased by 5 percent. These adjustments
to the case-mix weights were finalized in the CY 2012 HH PPS final rule
(76 FR 68557) and were done to address MedPAC's concerns that the HH
PPS overvalues therapy episodes and undervalues non-therapy episodes
and to better align the case-mix weights with episode costs estimated
from cost report data.\9\
---------------------------------------------------------------------------
\9\ Medicare Payment Advisory Commission (MedPAC), Report to the
Congress: Medicare Payment Policy. March 2011, p. 176.
---------------------------------------------------------------------------
Step 6: After the adjustments in Step 5 are applied to the raw
weights, the weights are further adjusted to create an increase in the
payment weights for the therapy visit steps between the therapy
thresholds. Weights with the same clinical severity level, functional
severity level, and early/later episode status were grouped together.
Then within those groups, the weights for each therapy step between
thresholds are gradually increased. We do this by interpolating between
the main thresholds on the model (from 0 to 5 to 14 to 15 therapy
visits, and from 14 to 15 to 20+ therapy visits). We use a linear model
to implement the interpolation so the payment weight increase for each
step between the thresholds (such as the increase between 0 and 5
therapy visits and 6 therapy visits and the increase between 6 therapy
visits and 7 to 9 therapy visits) are constant. This interpolation is
identical to the process finalized in the CY 2012 HH PPS final rule (76
FR 68555).
Step 7: The interpolated weights are then adjusted so that the
average case-mix for the weights is equal to 1.0000.\10\ This last step
creates the final CY 2018 case-mix weights shown in Table 5.
---------------------------------------------------------------------------
\10\ When computing the average, we compute a weighted average,
assigning a value of one to each normal episode and a value equal to
the episode length divided by 60 for PEPs.
[[Page 51687]]
Table 5--CY 2018 Case-Mix Payment Weights
----------------------------------------------------------------------------------------------------------------
Clinical and functional levels
Pay group Description (1 = Low; 2 = Medium; 3 = High) CY 2018 weight
----------------------------------------------------------------------------------------------------------------
10111............................ 1st and 2nd Episodes, 0 to 5 C1F1S1 0.5595
Therapy Visits.
10112............................ 1st and 2nd Episodes, 6 C1F1S2 0.6911
Therapy Visits.
10113............................ 1st and 2nd Episodes, 7 to 9 C1F1S3 0.8227
Therapy Visits.
10114............................ 1st and 2nd Episodes, 10 C1F1S4 0.9543
Therapy Visits.
10115............................ 1st and 2nd Episodes, 11 to C1F1S5 1.0859
13 Therapy Visits.
10121............................ 1st and 2nd Episodes, 0 to 5 C1F2S1 0.6640
Therapy Visits.
10122............................ 1st and 2nd Episodes, 6 C1F2S2 0.7832
Therapy Visits.
10123............................ 1st and 2nd Episodes, 7 to 9 C1F2S3 0.9025
Therapy Visits.
10124............................ 1st and 2nd Episodes, 10 C1F2S4 1.0217
Therapy Visits.
10125............................ 1st and 2nd Episodes, 11 to C1F2S5 1.1409
13 Therapy Visits.
10131............................ 1st and 2nd Episodes, 0 to 5 C1F3S1 0.7139
Therapy Visits.
10132............................ 1st and 2nd Episodes, 6 C1F3S2 0.8302
Therapy Visits.
10133............................ 1st and 2nd Episodes, 7 to 9 C1F3S3 0.9466
Therapy Visits.
10134............................ 1st and 2nd Episodes, 10 C1F3S4 1.0629
Therapy Visits.
10135............................ 1st and 2nd Episodes, 11 to C1F3S5 1.1792
13 Therapy Visits.
10211............................ 1st and 2nd Episodes, 0 to 5 C2F1S1 0.5948
Therapy Visits.
10212............................ 1st and 2nd Episodes, 6 C2F1S2 0.7325
Therapy Visits.
10213............................ 1st and 2nd Episodes, 7 to 9 C2F1S3 0.8703
Therapy Visits.
10214............................ 1st and 2nd Episodes, 10 C2F1S4 1.0080
Therapy Visits.
10215............................ 1st and 2nd Episodes, 11 to C2F1S5 1.1457
13 Therapy Visits.
10221............................ 1st and 2nd Episodes, 0 to 5 C2F2S1 0.6994
Therapy Visits.
10222............................ 1st and 2nd Episodes, 6 C2F2S2 0.8247
Therapy Visits.
10223............................ 1st and 2nd Episodes, 7 to 9 C2F2S3 0.9500
Therapy Visits.
10224............................ 1st and 2nd Episodes, 10 C2F2S4 1.0753
Therapy Visits.
10225............................ 1st and 2nd Episodes, 11 to C2F2S5 1.2007
13 Therapy Visits.
10231............................ 1st and 2nd Episodes, 0 to 5 C2F3S1 0.7493
Therapy Visits.
10232............................ 1st and 2nd Episodes, 6 C2F3S2 0.8717
Therapy Visits.
10233............................ 1st and 2nd Episodes, 7 to 9 C2F3S3 0.9941
Therapy Visits.
10234............................ 1st and 2nd Episodes, 10 C2F3S4 1.1166
Therapy Visits.
10235............................ 1st and 2nd Episodes, 11 to C2F3S5 1.2390
13 Therapy Visits.
10311............................ 1st and 2nd Episodes, 0 to 5 C3F1S1 0.6374
Therapy Visits.
10312............................ 1st and 2nd Episodes, 6 C3F1S2 0.7902
Therapy Visits.
10313............................ 1st and 2nd Episodes, 7 to 9 C3F1S3 0.9429
Therapy Visits.
10314............................ 1st and 2nd Episodes, 10 C3F1S4 1.0957
Therapy Visits.
10315............................ 1st and 2nd Episodes, 11 to C3F1S5 1.2484
13 Therapy Visits.
10321............................ 1st and 2nd Episodes, 0 to 5 C3F2S1 0.7420
Therapy Visits.
10322............................ 1st and 2nd Episodes, 6 C3F2S2 0.8823
Therapy Visits.
10323............................ 1st and 2nd Episodes, 7 to 9 C3F2S3 1.0227
Therapy Visits.
10324............................ 1st and 2nd Episodes, 10 C3F2S4 1.1630
Therapy Visits.
10325............................ 1st and 2nd Episodes, 11 to C3F2S5 1.3034
13 Therapy Visits.
10331............................ 1st and 2nd Episodes, 0 to 5 C3F3S1 0.7919
Therapy Visits.
10332............................ 1st and 2nd Episodes, 6 C3F3S2 0.9293
Therapy Visits.
10333............................ 1st and 2nd Episodes, 7 to 9 C3F3S3 1.0668
Therapy Visits.
10334............................ 1st and 2nd Episodes, 10 C3F3S4 1.2042
Therapy Visits.
10335............................ 1st and 2nd Episodes, 11 to C3F3S5 1.3417
13 Therapy Visits.
21111............................ 1st and 2nd Episodes, 14 to C1F1S1 1.2176
15 Therapy Visits.
21112............................ 1st and 2nd Episodes, 16 to C1F1S2 1.3807
17 Therapy Visits.
21113............................ 1st and 2nd Episodes, 18 to C1F1S3 1.5439
19 Therapy Visits.
21121............................ 1st and 2nd Episodes, 14 to C1F2S1 1.2601
15 Therapy Visits.
21122............................ 1st and 2nd Episodes, 16 to C1F2S2 1.4213
17 Therapy Visits.
21123............................ 1st and 2nd Episodes, 18 to C1F2S3 1.5826
19 Therapy Visits.
21131............................ 1st and 2nd Episodes, 14 to C1F3S1 1.2955
15 Therapy Visits.
21132............................ 1st and 2nd Episodes, 16 to C1F3S2 1.4600
17 Therapy Visits.
21133............................ 1st and 2nd Episodes, 18 to C1F3S3 1.6244
19 Therapy Visits.
21211............................ 1st and 2nd Episodes, 14 to C2F1S1 1.2835
15 Therapy Visits.
21212............................ 1st and 2nd Episodes, 16 to C2F1S2 1.4598
17 Therapy Visits.
21213............................ 1st and 2nd Episodes, 18 to C2F1S3 1.6361
19 Therapy Visits.
21221............................ 1st and 2nd Episodes, 14 to C2F2S1 1.3260
15 Therapy Visits.
21222............................ 1st and 2nd Episodes, 16 to C2F2S2 1.5004
17 Therapy Visits.
21223............................ 1st and 2nd Episodes, 18 to C2F2S3 1.6748
19 Therapy Visits.
21231............................ 1st and 2nd Episodes, 14 to C2F3S1 1.3614
15 Therapy Visits.
21232............................ 1st and 2nd Episodes, 16 to C2F3S2 1.5390
17 Therapy Visits.
21233............................ 1st and 2nd Episodes, 18 to C2F3S3 1.7166
19 Therapy Visits.
21311............................ 1st and 2nd Episodes, 14 to C3F1S1 1.4012
15 Therapy Visits.
21312............................ 1st and 2nd Episodes, 16 to C3F1S2 1.6188
17 Therapy Visits.
21313............................ 1st and 2nd Episodes, 18 to C3F1S3 1.8364
19 Therapy Visits.
21321............................ 1st and 2nd Episodes, 14 to C3F2S1 1.4437
15 Therapy Visits.
21322............................ 1st and 2nd Episodes, 16 to C3F2S2 1.6594
17 Therapy Visits.
[[Page 51688]]
21323............................ 1st and 2nd Episodes, 18 to C3F2S3 1.8751
19 Therapy Visits.
21331............................ 1st and 2nd Episodes, 14 to C3F3S1 1.4791
15 Therapy Visits.
21332............................ 1st and 2nd Episodes, 16 to C3F3S2 1.6981
17 Therapy Visits.
21333............................ 1st and 2nd Episodes, 18 to C3F3S3 1.9170
19 Therapy Visits.
22111............................ 3rd+ Episodes, 14 to 15 C1F1S1 1.2328
Therapy Visits.
22112............................ 3rd+ Episodes, 16 to 17 C1F1S2 1.3909
Therapy Visits.
22113............................ 3rd+ Episodes, 18 to 19 C1F1S3 1.5489
Therapy Visits.
22121............................ 3rd+ Episodes, 14 to 15 C1F2S1 1.2619
Therapy Visits.
22122............................ 3rd+ Episodes, 16 to 17 C1F2S2 1.4225
Therapy Visits.
22123............................ 3rd+ Episodes, 18 to 19 C1F2S3 1.5832
Therapy Visits.
22131............................ 3rd+ Episodes, 14 to 15 C1F3S1 1.3088
Therapy Visits.
22132............................ 3rd+ Episodes, 16 to 17 C1F3S2 1.4688
Therapy Visits.
22133............................ 3rd+ Episodes, 18 to 19 C1F3S3 1.6288
Therapy Visits.
22211............................ 3rd++ Episodes, 14 to 15 C2F1S1 1.2860
Therapy Visits.
22212............................ 3rd+ Episodes, 16 to 17 C2F1S2 1.4615
Therapy Visits.
22213............................ 3rd+ Episodes, 18 to 19 C2F1S3 1.6369
Therapy Visits.
22221............................ 3rd+ Episodes, 14 to 15 C2F2S1 1.3151
Therapy Visits.
22222............................ 3rd+ Episodes, 16 to 17 C2F2S2 1.4931
Therapy Visits.
22223............................ 3rd+ Episodes, 18 to 19 C2F2S3 1.6712
Therapy Visits.
22231............................ 3rd+ Episodes, 14 to 15 C2F3S1 1.3620
Therapy Visits.
22232............................ 3rd+ Episodes, 16 to 17 C2F3S2 1.5394
Therapy Visits.
22233............................ 3rd+ Episodes, 18 to 19 C2F3S3 1.7168
Therapy Visits.
22311............................ 3rd+ Episodes, 14 to 15 C3F1S1 1.4951
Therapy Visits.
22312............................ 3rd+ Episodes, 16 to 17 C3F1S2 1.6814
Therapy Visits.
22313............................ 3rd+ Episodes, 18 to 19 C3F1S3 1.8677
Therapy Visits.
22321............................ 3rd+ Episodes, 14 to 15 C3F2S1 1.5241
Therapy Visits.
22322............................ 3rd+ Episodes, 16 to 17 C3F2S2 1.7130
Therapy Visits.
22323............................ 3rd+ Episodes, 18 to 19 C3F2S3 1.9019
Therapy Visits.
22331............................ 3rd+ Episodes, 14 to 15 C3F3S1 1.5710
Therapy Visits.
22332............................ 3rd+ Episodes, 16 to 17 C3F3S2 1.7593
Therapy Visits.
22333............................ 3rd+ Episodes, 18 to 19 C3F3S3 1.9476
Therapy Visits.
30111............................ 3rd+ Episodes, 0 to 5 C1F1S1 0.4557
Therapy Visits.
30112............................ 3rd+ Episodes, 6 Therapy C1F1S2 0.6111
Visits.
30113............................ 3rd+ Episodes, 7 to 9 C1F1S3 0.7666
Therapy Visits.
30114............................ 3rd+ Episodes, 10 Therapy C1F1S4 0.9220
Visits.
30115............................ 3rd+ Episodes, 11 to 13 C1F1S5 1.0774
Therapy Visits.
30121............................ 3rd+ Episodes, 0 to 5 C1F2S1 0.5407
Therapy Visits.
30122............................ 3rd+ Episodes, 6 Therapy C1F2S2 0.6850
Visits.
30123............................ 3rd+ Episodes, 7 to 9 C1F2S3 0.8292
Therapy Visits.
30124............................ 3rd+ Episodes, 10 Therapy C1F2S4 0.9734
Visits.
30125............................ 3rd+ Episodes, 11 to 13 C1F2S5 1.1177
Therapy Visits.
30131............................ 3rd+ Episodes, 0 to 5 C1F3S1 0.5856
Therapy Visits.
30132............................ 3rd+ Episodes, 6 Therapy C1F3S2 0.7303
Visits.
30133............................ 3rd+ Episodes, 7 to 9 C1F3S3 0.8749
Therapy Visits.
30134............................ 3rd+ Episodes, 10 Therapy C1F3S4 1.0195
Visits.
30135............................ 3rd+ Episodes, 11 to 13 C1F3S5 1.1642
Therapy Visits.
30211............................ 3rd+ Episodes, 0 to 5 C2F1S1 0.4802
Therapy Visits.
30212............................ 3rd+ Episodes, 6 Therapy C2F1S2 0.6414
Visits.
30213............................ 3rd+ Episodes, 7 to 9 C2F1S3 0.8025
Therapy Visits.
30214............................ 3rd+ Episodes, 10 Therapy C2F1S4 0.9637
Visits.
30215............................ 3rd+ Episodes, 11 to 13 C2F1S5 1.1249
Therapy Visits.
30221............................ 3rd+ Episodes, 0 to 5 C2F2S1 0.5652
Therapy Visits.
30222............................ 3rd+ Episodes, 6 Therapy C2F2S2 0.7152
Visits.
30223............................ 3rd+ Episodes, 7 to 9 C2F2S3 0.8652
Therapy Visits.
30224............................ 3rd+ Episodes, 10 Therapy C2F2S4 1.0151
Visits.
30225............................ 3rd+ Episodes, 11 to 13 C2F2S5 1.1651
Therapy Visits.
30231............................ 3rd+ Episodes, 0 to 5 C2F3S1 0.6101
Therapy Visits.
30232............................ 3rd+ Episodes, 6 Therapy C2F3S2 0.7605
Visits.
30233............................ 3rd+ Episodes, 7 to 9 C2F3S3 0.9109
Therapy Visits.
30234............................ 3rd+ Episodes, 10 Therapy C2F3S4 1.0612
Visits.
30235............................ 3rd+ Episodes, 11 to 13 C2F3S5 1.2116
Therapy Visits.
30311............................ 3rd+ Episodes, 0 to 5 C3F1S1 0.5936
Therapy Visits.
30312............................ 3rd+ Episodes, 6 Therapy C3F1S2 0.7739
Visits.
30313............................ 3rd+ Episodes, 7 to 9 C3F1S3 0.9542
Therapy Visits.
30314............................ 3rd+ Episodes, 10 Therapy C3F1S4 1.1345
Visits.
30315............................ 3rd+ Episodes, 11 to 13 C3F1S5 1.3148
Therapy Visits.
30321............................ 3rd+ Episodes, 0 to 5 C3F2S1 0.6786
Therapy Visits.
30322............................ 3rd+ Episodes, 6 Therapy C3F2S2 0.8477
Visits.
[[Page 51689]]
30323............................ 3rd+ Episodes, 7 to 9 C3F2S3 1.0168
Therapy Visits.
30324............................ 3rd+ Episodes, 10 Therapy C3F2S4 1.1859
Visits.
30325............................ 3rd+ Episodes, 11 to 13 C3F2S5 1.3550
Therapy Visits.
30331............................ 3rd+ Episodes, 0 to 5 C3F3S1 0.7235
Therapy Visits.
30332............................ 3rd+ Episodes, 6 Therapy C3F3S2 0.8930
Visits.
30333............................ 3rd+ Episodes, 7 to 9 C3F3S3 1.0625
Therapy Visits.
30334............................ 3rd+ Episodes, 10 Therapy C3F3S4 1.2320
Visits.
30335............................ 3rd+ Episodes, 11 to 13 C3F3S5 1.4015
Therapy Visits.
40111............................ All Episodes, 20+ Therapy C1F1S1 1.7070
Visits.
40121............................ All Episodes, 20+ Therapy C1F2S1 1.7438
Visits.
40131............................ All Episodes, 20+ Therapy C1F3S1 1.7888
Visits.
40211............................ All Episodes, 20+ Therapy C2F1S1 1.8124
Visits.
40221............................ All Episodes, 20+ Therapy C2F2S1 1.8492
Visits.
40231............................ All Episodes, 20+ Therapy C2F3S1 1.8942
Visits.
40311............................ All Episodes, 20+ Therapy C3F1S1 2.0540
Visits.
40321............................ All Episodes, 20+ Therapy C3F2S1 2.0908
Visits.
40331............................ All Episodes, 20+ Therapy C3F3S1 2.1359
Visits.
----------------------------------------------------------------------------------------------------------------
To ensure the changes to the HH PPS case-mix weights are
implemented in a budget neutral manner, we then apply a case-mix budget
neutrality factor to the CY 2018 national, standardized 60-day episode
payment rate (see section III.C.3. of this final rule). The case-mix
budget neutrality factor is calculated as the ratio of total payments
when the CY 2018 HH PPS case-mix weights (developed using CY 2016 home
health claims data) are applied to CY 2016 utilization (claims) data to
total payments when CY 2017 HH PPS case-mix weights (developed using CY
2015 home health claims data) are applied to CY 2016 utilization data.
This produces a case-mix budget neutrality factor for CY 2018 of
1.0160.
The following is a summary of the comments and our responses to
comments on the CY 2018 case-mix weights:
Comment: A few commenters stated that CMS did not provide
sufficient transparency of the details and methods used to recalibrate
the HH PPS case-mix weights in the proposed rule. In addition,
commenters stated that CMS provided little justification for
recalibrating the case-mix weights just 1 year following the
recalibration of case-mix weights in CY 2017, 2 years since the
recalibration in 2016, and 5 years since the recalibration for the CY
2012 HH PPS final rule. The commenters noted that they opposed the
recalibration of the case weights for CY 2018, but supported the budget
neutrality adjustment to account for the recalibrated case-mix weights
if CMS finalizes the recalibration.
Response: As stated in the CY 2018 HH PPS proposed rule (82 FR
35282), the methodology used to recalibrate the weights is identical to
the methodology used in the CY 2012 recalibration except for the minor
exceptions as noted in the CY 2015 HH PPS proposed and final rules (79
FR 38366 and 79 FR 66032, respectively). In the CY 2015 HH PPS final
rule, we finalized annual recalibration and the methodology to be used
for each year's recalibration (79 FR 66072). For more detail, we also
encourage commenters to refer to the CY 2012 HH PPS proposed and final
rules (76 FR 40988 and 76 FR 68526, respectively) and the November 1,
2011 ``Revision of the Case-Mix Weights for the HH PPS Report'' on our
home page at: https://www.cms.gov/center/provider-Type/home-Health-Agency-HHA-Center.html for additional information about the
recalibration methodology.
We note that in comparing the final CY 2018 HH PPS case-mix weights
(see Table 5) to the final CY 2015 HH PPS case-mix weights (79 FR
66062), the case-mix weights change very little, with most case-mix
weights either increasing or decreasing by 1 to 2 percent with no case-
mix weights increasing by more than 3 percent or decreasing by more
than 3 percent. The aggregate decreases in the case-mix weights are
offset by the case-mix budget neutrality factor, which is applied to
the national, standardized 60-day episode payment rate. In other words,
although the case-mix weights themselves may increase or decrease from
year-to-year, we correspondingly offset any estimated increases or
decreases in total payments under the HH PPS, as a result of the case-
mix recalibration, by applying a budget neutrality factor to the
national, standardized 60-day episode payment rate. For CY 2018, the
case-mix budget neutrality factor will be 1.0160 as described
previously. The recalibration of the case-mix weights is not intended
to increase or decrease overall HH PPS payments, but rather is used to
update the relative differences in resource use amongst the 153 groups
in the HH PPS case-mix system and maintain the level of aggregate
payments before application of any other adjustments. We will continue
to monitor the performance of any finalized case-mix model, and will
make changes to it as necessary.
Final Decision: We are finalizing the recalibrated scores for the
case-mix adjustment variables, clinical and functional thresholds,
payment regression model, and case-mix weights in Tables 2 through 5.
For this final rule, the CY 2018 scores for the case-mix variables, the
clinical and functional thresholds, and the case-mix weights were
developed using complete CY 2016 claims data as of August 17, 2017. We
note that we finalized the recalibration methodology and the proposal
to annually recalibrate the HH PPS case-mix weights in the CY 2015 HH
PPS final rule (79 FR 66072). No additional proposals were made with
regard to the recalibration methodology in the CY 2018 HH PPS proposed
rule.
[[Page 51690]]
C. CY 2018 Home Health Payment Rate Update
1. CY 2018 Home Health Market Basket Update
Section 1895(b)(3)(B) of the Act requires that the standard
prospective payment amounts for CY 2018 be increased by a factor equal
to the applicable HH market basket update for those HHAs that submit
quality data as required by the Secretary. The home health market
basket was rebased and revised in CY 2013. A detailed description of
how we derive the HHA market basket is available in the CY 2013 HH PPS
final rule (77 FR 67080 through 67090).
Section 1895(b)(3)(B)(vi) of the Act, requires that, in CY 2015
(and in subsequent calendar years, except CY 2018 (under section 411(c)
of the Medicare Access and CHIP Reauthorization Act of 2015 (MACRA)
(Pub. L. 114-10, enacted April 16, 2015)), the market basket percentage
under the HHA prospective payment system as described in section
1895(b)(3)(B) of the Act be annually adjusted by changes in economy-
wide productivity. Section 1886(b)(3)(B)(xi)(II) of the Act defines the
productivity adjustment to be equal to the 10-year moving average of
change in annual economy-wide private nonfarm business multifactor
productivity (MFP) (as projected by the Secretary for the 10-year
period ending with the applicable fiscal year, calendar year, cost
reporting period, or other annual period) (the ``MFP adjustment''). The
Bureau of Labor Statistics (BLS) is the agency that publishes the
official measure of private nonfarm business MFP. Please see https://www.bls.gov/mfp to obtain the BLS historical published MFP data.
Prior to the enactment of the MACRA, which amended section
1895(b)(3)(B) of the Act, the home health update percentage for CY 2018
would have been based on the estimated home health market basket update
of 2.5 percent (based on IHS Global Inc.'s third-quarter 2017 forecast
with historical data through second-quarter 2017). Due to the
requirements specified at section 1895(b)(3)(B)(vi) of the Act prior to
the enactment of MACRA, the estimated CY 2018 home health market basket
update of 2.5 percent would have been reduced by a MFP adjustment as
mandated by the Affordable Care Act (currently estimated to be 0.6
percentage point for CY 2018). In effect, the home health payment
update percentage for CY 2018 would have been 1.9 percent. However,
section 411(c) of the MACRA amended section 1895(b)(3)(B) of the Act,
such that, for home health payments for CY 2018, the market basket
percentage increase is required to be 1 percent.
Section 1895(b)(3)(B) of the Act requires that the home health
update be decreased by 2 percentage points for those HHAs that do not
submit quality data as required by the Secretary. For HHAs that do not
submit the required quality data for CY 2018, the home health payment
update will be -1 percent (1 percent minus 2 percentage points).
2. CY 2018 Home Health Wage Index
Sections 1895(b)(4)(A)(ii) and (b)(4)(C) of the Act require the
Secretary to provide appropriate adjustments to the proportion of the
payment amount under the HH PPS that account for area wage differences,
using adjustment factors that reflect the relative level of wages and
wage-related costs applicable to the furnishing of HH services. Since
the inception of the HH PPS, we have used inpatient hospital wage data
in developing a wage index to be applied to HH payments. We proposed to
continue this practice for CY 2018, as we continue to believe that, in
the absence of HH-specific wage data, using inpatient hospital wage
data is appropriate and reasonable for the HH PPS. Specifically, we
proposed to continue to use the pre-floor, pre-reclassified hospital
wage index as the wage adjustment to the labor portion of the HH PPS
rates. For CY 2018, the updated wage data are for hospital cost
reporting periods beginning on or after October 1, 2013, and before
October 1, 2014 (FY 2014 cost report data). We apply the appropriate
wage index value to the labor portion of the HH PPS rates based on the
site of service for the beneficiary (defined by section 1861(m) of the
Act as the beneficiary's place of residence).
To address those geographic areas in which there are no inpatient
hospitals, and thus, no hospital wage data on which to base the
calculation of the CY 2018 HH PPS wage index, we proposed to continue
to use the same methodology discussed in the CY 2007 HH PPS final rule
(71 FR 65884) to address those geographic areas in which there are no
inpatient hospitals. For rural areas that do not have inpatient
hospitals, we proposed to use the average wage index from all
contiguous Core Based Statistical Areas (CBSAs) as a reasonable proxy.
Currently, the only rural area without a hospital from which hospital
wage data could be derived is Puerto Rico. However, for rural Puerto
Rico, we do not apply this methodology due to the distinct economic
circumstances that exist there (for example, due to the close proximity
to one another of almost all of Puerto Rico's various urban and non-
urban areas, this methodology would produce a wage index for rural
Puerto Rico that is higher than that in half of its urban areas).
Instead, we proposed to continue to use the most recent wage index
previously available for that area. For urban areas without inpatient
hospitals, we use the average wage index of all urban areas within the
state as a reasonable proxy for the wage index for that CBSA. For CY
2018, the only urban area without inpatient hospital wage data is
Hinesville, GA (CBSA 25980).
On February 28, 2013, OMB issued Bulletin No. 13-01, announcing
revisions to the delineations of MSAs, Micropolitan Statistical Areas,
and CBSAs, and guidance on uses of the delineation of these areas. In
the CY 2015 HH PPS final rule (79 FR 66085 through 66087), we adopted
the OMB's new area delineations using a 1-year transition. The most
recent bulletin (No. 15-01) concerning the revised delineations was
published by the OMB on July 15, 2015.
The CY 2018 wage index is available on the CMS Web site at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/HomeHealthPPS/Home-Health-Prospective-Payment-System-Regulations-and-Notices.html.
3. CY 2018 Annual Payment Update
a. Background
The Medicare HH PPS has been in effect since October 1, 2000. As
set forth in the July 3, 2000 final rule (65 FR 41128), the base unit
of payment under the Medicare HH PPS is a national, standardized 60-day
episode payment rate. As set forth in Sec. 484.220, we adjust the
national, standardized 60-day episode payment rate by a case-mix
relative weight and a wage index value based on the site of service for
the beneficiary.
To provide appropriate adjustments to the proportion of the payment
amount under the HH PPS to account for area wage differences, we apply
the appropriate wage index value to the labor portion of the HH PPS
rates. The labor-related share of the case-mix adjusted 60-day episode
rate will continue to be 78.535 percent and the non-labor-related share
will continue to be 21.465 percent as set out in the CY 2013 HH PPS
final rule (77 FR 67068). The CY 2018 HH PPS rates use the same case-
mix methodology as set forth in the CY 2008 HH PPS final rule with
comment period (72 FR 49762) and will be adjusted as described in
section III.B.
[[Page 51691]]
of this final rule. The following are the steps we take to compute the
case-mix and wage-adjusted 60-day episode rate:
(1) Multiply the national 60-day episode rate by the patient's
applicable case-mix weight.
(2) Divide the case-mix adjusted amount into a labor (78.535
percent) and a non-labor portion (21.465 percent).
(3) Multiply the labor portion by the applicable wage index based
on the site of service of the beneficiary.
(4) Add the wage-adjusted portion to the non-labor portion,
yielding the case-mix and wage adjusted 60-day episode rate, subject to
any additional applicable adjustments.
In accordance with section 1895(b)(3)(B) of the Act, we proposed
the annual update of the HH PPS rates. Section 484.225 sets forth the
specific annual percentage update methodology. In accordance with Sec.
484.225(i), for a HHA that does not submit HH quality data, as
specified by the Secretary, the unadjusted national prospective 60-day
episode rate is equal to the rate for the previous calendar year
increased by the applicable HH market basket index amount minus 2
percentage points. Any reduction of the percentage change will apply
only to the calendar year involved and will not be considered in
computing the prospective payment amount for a subsequent calendar
year.
Medicare pays the national, standardized 60-day case-mix and wage-
adjusted episode payment on a split percentage payment approach. The
split percentage payment approach includes an initial percentage
payment and a final percentage payment as set forth in Sec.
484.205(b)(1) and (b)(2). We may base the initial percentage payment on
the submission of a request for anticipated payment (RAP) and the final
percentage payment on the submission of the claim for the episode, as
discussed in Sec. 409.43. The claim for the episode that the HHA
submits for the final percentage payment determines the total payment
amount for the episode and whether we make an applicable adjustment to
the 60-day case-mix and wage-adjusted episode payment. The end date of
the 60-day episode as reported on the claim determines which calendar
year rates Medicare will use to pay the claim.
We may also adjust the 60-day case-mix and wage-adjusted episode
payment based on the information submitted on the claim to reflect the
following:
A low-utilization payment adjustment (LUPA) is provided on
a per-visit basis as set forth in Sec. Sec. 484.205(c) and 484.230.
A partial episode payment (PEP) adjustment as set forth in
Sec. Sec. 484.205(d) and 484.235.
An outlier payment as set forth in Sec. Sec. 484.205(e)
and 484.240.
b. CY 2018 National, Standardized 60-Day Episode Payment Rate
Section 1895(b)(3)(A)(i) of the Act requires that the 60-day
episode base rate and other applicable amounts be standardized in a
manner that eliminates the effects of variations in relative case-mix
and area wage adjustments among different home health agencies in a
budget neutral manner. To determine the CY 2018 national, standardized
60-day episode payment rate, we apply a wage index budget neutrality
factor; a case-mix budget neutrality factor described in section III.B.
of this final rule; a reduction of 0.97 percent to account for nominal
case-mix growth from 2012 to 2014, as finalized in the CY 2016 HH PPS
final rule (80 FR 68646); and the home health payment update percentage
discussed in section III.C.1 of this final rule.
To calculate the wage index budget neutrality factor, we simulated
total payments for non-LUPA episodes using the CY 2018 wage index and
compared it to our simulation of total payments for non-LUPA episodes
using the CY 2017 wage index. By dividing the total payments for non-
LUPA episodes using the CY 2018 wage index by the total payments for
non-LUPA episodes using the CY 2017 wage index, we obtain a wage index
budget neutrality factor of 1.0004. We will apply the wage index budget
neutrality factor of 1.0004 to the calculation of the CY 2018 national,
standardized 60-day episode rate.
As discussed in section III.B. of the proposed rule, to ensure the
changes to the case-mix weights are implemented in a budget neutral
manner, we proposed to apply a case-mix weight budget neutrality factor
to the CY 2018 national, standardized 60-day episode payment rate. The
case-mix weight budget neutrality factor is calculated as the ratio of
total payments when CY 2018 case-mix weights are applied to CY 2016
utilization (claims) data to total payments when CY 2017 case-mix
weights are applied to CY 2016 utilization data. The case-mix budget
neutrality factor for CY 2018 is 1.0160 as described in section III.B
of this final rule.
Next, we apply a reduction of 0.97 percent to the national,
standardized 60-day payment rate for CY 2018 to account for nominal
case-mix growth between CY 2012 and CY 2014. Lastly, we will update the
payment rates by the CY 2018 home health payment update percentage of 1
percent as mandated by section 1895(b)(3)(B)(iii) of the Act. The CY
2018 national, standardized 60-day episode payment rate is calculated
in Table 6.
Table 6--CY 2018 60-Day National, Standardized 60-Day Episode Payment Amount
--------------------------------------------------------------------------------------------------------------------------------------------------------
CY 2018
Wage index Case-mix Nominal case- national,
CY 2017 national, standardized 60-day episode payment budget weights budget mix growth CY 2018 HH standardized
neutrality neutrality adjustment (1- payment update 60-day episode
factor factor 0.0097) payment
--------------------------------------------------------------------------------------------------------------------------------------------------------
$2,989.97.......................................................... x 1.0004 x 1.0160 x 0.9903 x 1.01 $3,039.64
--------------------------------------------------------------------------------------------------------------------------------------------------------
The CY 2018 national, standardized 60-day episode payment rate for
an HHA that does not submit the required quality data is updated by the
CY 2018 home health payment update of 1 percent minus 2 percentage
points and is shown in Table 7.
[[Page 51692]]
Table 7--CY 2017 National, Standardized 60-Day Episode Payment Amount for HHAS That Do Not Submit the Quality Data
--------------------------------------------------------------------------------------------------------------------------------------------------------
CY 2018
Wage index Case-mix Nominal case- national,
CY 2017 national, standardized 60-day episode payment budget weights budget mix growth CY 2018 HH standardized
neutrality neutrality adjustment (1- payment update 60-day episode
factor factor 0.0097) payment
--------------------------------------------------------------------------------------------------------------------------------------------------------
$2,989.97.......................................................... x 1.0004 x 1.0160 x 0.9903 x 0.99 $2,979.45
--------------------------------------------------------------------------------------------------------------------------------------------------------
c. CY 2018 National Per-Visit Rates
The national per-visit rates are used to pay LUPAs (episodes with
four or fewer visits) and are also used to compute imputed costs in
outlier calculations. The per-visit rates are paid by type of visit or
HH discipline. The six HH disciplines are as follows:
Home health aide (HH aide).
Medical Social Services (MSS).
Occupational therapy (OT).
Physical therapy (PT).
Skilled nursing (SN).
Speech-language pathology (SLP).
To calculate the CY 2018 national per-visit rates, we started with
the CY 2017 national per-visit rates. Then we applied a wage index
budget neutrality factor to ensure budget neutrality for LUPA per-visit
payments. We calculated the wage index budget neutrality factor by
simulating total payments for LUPA episodes using the CY 2018 wage
index and comparing it to simulated total payments for LUPA episodes
using the CY 2017 wage index. By dividing the total payments for LUPA
episodes using the CY 2018 wage index by the total payments for LUPA
episodes using the CY 2017 wage index, we obtained a wage index budget
neutrality factor of 1.0010. We apply the wage index budget neutrality
factor of 1.0010 in order to calculate the CY 2018 national per-visit
rates.
The LUPA per-visit rates are not calculated using case-mix weights.
Therefore, there is no case-mix weights budget neutrality factor needed
to ensure budget neutrality for LUPA payments. Lastly, the per-visit
rates for each discipline are updated by the CY 2018 home health
payment update percentage of 1 percent. The national per-visit rates
are adjusted by the wage index based on the site of service of the
beneficiary. The per-visit payments for LUPAs are separate from the
LUPA add-on payment amount, which is paid for episodes that occur as
the only episode or initial episode in a sequence of adjacent episodes.
The CY 2018 national per-visit rates are shown in Tables 8 and 9.
Table 8--CY 2018 National Per-Visit Payment Amounts for HHAS That Do Submit the Required Quality Data
----------------------------------------------------------------------------------------------------------------
Wage index
CY 2017 per- budget CY 2018 HH CY 2018 per-
HH Discipline visit payment neutrality payment visit payment
factor update
----------------------------------------------------------------------------------------------------------------
Home Health Aide................................ $64.23 x 1.0010 x 1.01 $64.94
Medical Social Services......................... 227.36 x 1.0010 x 1.01 229.86
Occupational Therapy............................ 156.11 x 1.0010 x 1.01 157.83
Physical Therapy................................ 155.05 x 1.0010 x 1.01 156.76
Skilled Nursing................................. 141.84 x 1.0010 x 1.01 143.40
Speech-Language Pathology....................... 168.52 x 1.0010 x 1.01 170.38
----------------------------------------------------------------------------------------------------------------
The CY 2018 per-visit payment rates for HHAs that do not submit the
required quality data are updated by the CY 2018 HH payment update
percentage of 1 percent minus 2 percentage points and are shown in
Table 9.
Table 9--CY 2018 National Per-Visit Payment Amounts for HHAS That Do Not Submit the Required Quality Data
----------------------------------------------------------------------------------------------------------------
CY 2018 HH
Wage index payment
HH Discipline CY 2017 per- budget update minus CY 2018 per-
visit rates neutrality 2 percentage visit rates
factor points
----------------------------------------------------------------------------------------------------------------
Home Health Aide................................ $64.23 x 1.0010 x 0.99 $63.65
Medical Social Services......................... 227.36 x 1.0010 x 0.99 225.31
Occupational Therapy............................ 156.11 x 1.0010 x 0.99 154.70
Physical Therapy................................ 155.05 x 1.0010 x 0.99 153.65
Skilled Nursing................................. 141.84 x 1.0010 x 0.99 140.56
Speech-Language Pathology....................... 168.52 x 1.0010 x 0.99 167.00
----------------------------------------------------------------------------------------------------------------
[[Page 51693]]
d. Low-Utilization Payment Adjustment (LUPA) Add-On Factors
LUPA episodes that occur as the only episode or as an initial
episode in a sequence of adjacent episodes are adjusted by applying an
additional amount to the LUPA payment before adjusting for area wage
differences. In the CY 2014 HH PPS final rule (78 FR 72305), we changed
the methodology for calculating the LUPA add-on amount by finalizing
the use of three LUPA add-on factors: 1.8451 for SN; 1.6700 for PT; and
1.6266 for SLP. We multiply the per-visit payment amount for the first
SN, PT, or SLP visit in LUPA episodes that occur as the only episode or
an initial episode in a sequence of adjacent episodes by the
appropriate factor to determine the LUPA add-on payment amount. For
example, in the case of HHAs that do submit the required quality data,
for LUPA episodes that occur as the only episode or an initial episode
in a sequence of adjacent episodes, if the first skilled visit is SN,
the payment for that visit will be $264.59 (1.8451 multiplied by
$143.40), subject to area wage adjustment.
e. CY 2018 Non-Routine Medical Supply (NRS) Payment Rates
All medical supplies (routine and nonroutine) must be provided by
the HHA while the patient is under a home health plan of care. Examples
of supplies that can be considered non-routine include dressings for
wound care, I.V. supplies, ostomy supplies, catheters, and catheter
supplies. Payments for NRS are computed by multiplying the relative
weight for a particular severity level by the NRS conversion factor. To
determine the CY 2018 NRS conversion factor, we updated the CY 2017 NRS
conversion factor ($52.50) by the CY 2018 home health payment update
percentage of 1 percent. We did not apply a standardization factor as
the NRS payment amount calculated from the conversion factor is not
wage or case-mix adjusted when the final claim payment amount is
computed. The NRS conversion factor for CY 2018 is shown in Table 10.
Table 10--CY 2018 NRS Conversion Factor for HHAs That Do Submit the
Required Quality Data
------------------------------------------------------------------------
CY 2018 NRS
CY 2017 NRS conversion factor CY 2018 HH conversion
payment update factor
------------------------------------------------------------------------
$52.50................................ x 1.01 $53.03
------------------------------------------------------------------------
Using the CY 2018 NRS conversion factor, the payment amounts for
the six severity levels are shown in Table 11.
Table 11--CY 2018 NRS Payment Amounts for HHAs That Do Submit the Required Quality Data
----------------------------------------------------------------------------------------------------------------
CY 2018 NRS
Severity level Points (scoring) Relative payment
weight amounts
----------------------------------------------------------------------------------------------------------------
1........................................... 0................................. 0.2698 $14.31
2........................................... 1 to 14........................... 0.9742 51.66
3........................................... 15 to 27.......................... 2.6712 141.65
4........................................... 28 to 48.......................... 3.9686 210.45
5........................................... 49 to 98.......................... 6.1198 324.53
6........................................... 99+............................... 10.5254 558.16
----------------------------------------------------------------------------------------------------------------
For HHAs that do not submit the required quality data, we updated
the CY 2017 NRS conversion factor ($52.50) by the CY 2018 home health
payment update percentage of 1 percent minus 2 percentage points. The
CY 2018 NRS conversion factor for HHAs that do not submit quality data
is shown in Table 12.
Table 12--CY 2018 NRS Conversion Factor for HHAs That Do Not Submit the
Required Quality Data
------------------------------------------------------------------------
CY 2018 HH
payment update
percentage CY 2018 NRS
CY 2017 NRS conversion factor minus 2 conversion
percentage factor
points
------------------------------------------------------------------------
$52.50................................ x 0.99 $51.98
------------------------------------------------------------------------
The payment amounts for the various severity levels based on the
updated conversion factor for HHAs that do not submit quality data are
calculated in Table 13.
Table 13--CY 2018 NRS Payment Amounts for HHAs That Do Not Submit the Required Quality Data
----------------------------------------------------------------------------------------------------------------
CY 2018 NRS
Severity level Points (scoring) Relative payment
weight amounts
----------------------------------------------------------------------------------------------------------------
1........................................... 0................................. 0.2698 $14.02
2........................................... 1 to 14........................... 0.9742 50.64
3........................................... 15 to 27.......................... 2.6712 138.85
4........................................... 28 to 48.......................... 3.9686 206.29
5........................................... 49 to 98.......................... 6.1198 318.11
6........................................... 99+............................... 10.5254 547.11
----------------------------------------------------------------------------------------------------------------
[[Page 51694]]
f. Rural Add-On
Section 421(a) of the MMA required, for HH services furnished in a
rural area (as defined in section 1886(d)(2)(D) of the Act), for
episodes or visits ending on or after April 1, 2004, and before April
1, 2005, that the Secretary increase the payment amount that otherwise
would have been made under section 1895 of the Act for the services by
5 percent.
Section 5201 of the DRA amended section 421(a) of the MMA. The
amended section 421(a) of the MMA required, for HH services furnished
in a rural area (as defined in section 1886(d)(2)(D) of the Act), on or
after January 1, 2006, and before January 1, 2007, that the Secretary
increase the payment amount otherwise made under section 1895 of the
Act for those services by 5 percent.
Section 3131(c) of the Affordable Care Act amended section 421(a)
of the MMA to provide an increase of 3 percent of the payment amount
otherwise made under section 1895 of the Act for HH services furnished
in a rural area (as defined in section 1886(d)(2)(D) of the Act), for
episodes and visits ending on or after April 1, 2010, and before
January 1, 2016.
Section 210 of the MACRA amended section 421(a) of the MMA to
extend the rural add-on by providing an increase of 3 percent of the
payment amount otherwise made under section 1895 of the Act for HH
services provided in a rural area (as defined in section 1886(d)(2)(D)
of the Act), for episodes and visits ending before January 1, 2018.
Therefore, for episodes and visits that end on or after January 1,
2018, a rural add-on payment will not apply.
The following is a summary of the public comments received on the
``CY 2018 Home Health Payment Rate Update'' proposals and our
responses:
Comment: Several commenters stated that they wanted CMS to rescind
the nominal case-mix reduction for CY 2018. Some commenters stated that
implementation of the nominal case-mix reductions in 2016, 2017, and
2018 violated the limits on payment reductions set out by the Congress,
and urged CMS to adhere to the statutory limits on home health rate
cuts. Commenters expressed concerns with the data and methodology used
to develop the proposed case-mix cuts and stated that the annual
recalibration may have eliminated any practice of assigning an
inaccurate code to increase reimbursement and questioned the
interaction between the rebasing adjustments, nominal case-mix growth
reductions, and case-mix recalibration. A few commenters stated that
the baseline used in calculating the amount of case-mix growth was
inappropriate. Some commenters noted that actual program spending on
home health was consistently less than Congressional Budget Office
(CBO) estimates, and questioned CMS' authority to implement case mix
weight adjustments when home health spending was less than these
estimates. Commenters stated that there was no increase in aggregate
expenditures that warranted the application of this statutory
authority, and CMS should withdraw its proposal. Some commenters stated
that CMS should implement program integrity measures to control
aberrant coding by some providers instead of imposing across-the-board
case mix creep adjustments on all providers.
Response: We finalized the nominal case-mix reduction for CY 2018
in the CY 2016 HH PPS final rule. We did not propose changes to the
finalized reduction for CY 2018, nor did we propose any changes in the
methodology used to calculate nominal case-mix growth in the CY 2018 HH
PPS proposed rule. The majority of the comments received regarding the
payment reductions for nominal case-mix growth were very similar to the
comments submitted during the comment period for the CY 2016 HH PPS
proposed rule. Therefore, we encourage commenters to review our
responses to the comments we received on the payment reductions for
nominal case-mix growth in the CY 2016 HH PPS final rule (80 FR 68639
through 68646), which include responses on the interaction between the
rebasing and recalibration of the case-mix weights on the measurement
of nominal case-mix growth between 2012 and 2014, our rationale for the
methodology used to determine ``real'' versus ``nominal'' case-mix
growth in CYs 2012-2014, the role of CBO estimates in our determination
of nominal case-mix reductions, and our ability to target nominal case-
mix reductions to certain providers rather the industry as a whole. We
will continue to monitor real and nominal case-mix growth and may
propose additional reductions for nominal case-mix growth, as needed,
in the future.
Comment: MedPAC stated that they have long believed that it was
necessary for CMS to make adjustments to account for nominal case-mix
change to prevent additional overpayments. MedPAC stated that the CMS'
reduction to account for nominal case-mix growth is consistent with the
agency's past findings on trends in case-mix change in the payment
system and thus is warranted to ensure the accuracy of payments under
the home health PPS. MedPAC stated that a reduction of 0.97 percent
should not significantly affect access to care.
Response: We thank MedPAC for their comments.
Comment: Several commenters stated their belief that the CY 2018
payment update of 1 percent is inadequate.
Response: We appreciate the commenters' concerns. However, the 1
percent payment update for CY 2018 is mandated by section
1895(b)(3)(B)(iii) of the Act, as amended by section 411(c) of the
MACRA.
Comment: Several commenters urged CMS to continue providing rural
add-on payments in order that beneficiaries in rural communities
continue to have access to home health services.
Response: The sunset of rural add-on payments for CY 2018 is
statutory and we do not have the authority to re-authorize rural add-on
payments for episodes and visits ending on or after January 1,
2018.\11\ However, we plan to continue to monitor the costs associated
with providing home health care in rural versus urban areas. We note
that in Chapter 9 of its 2013 Report to Congress (available at https://medpac.gov/docs/default-source/reports/mar13_ch09.pdf?sfvrsn=0), MedPAC
stated that the use of the ``broadly targeted add-on, providing the
same payment for all rural areas regardless of access, results in rural
areas with the highest utilization drawing a disproportionate share of
the add-on payments.'' MedPAC stated that ``70 percent of the episodes
that received the add-on payments in 2011 were in rural counties with
utilization significantly higher than the national average'' and
recommended that Medicare target payment adjustments for rural areas to
those areas that have access challenges.
---------------------------------------------------------------------------
\11\ See U.S. CONST. art. I, Sec. 9 (``No money shall be drawn
from the Treasury, but in Consequence of Appropriations made by
Law'').
---------------------------------------------------------------------------
Comment: A commenter recommended that CMS explore policies that
provide Medicare coverage for services from therapy providers who
furnish telehealth services to their patients as proper application of
telehealth rehabilitation therapy services, particularly in underserved
areas, can potentially have a dramatic impact on improving care,
diminishing negative consequences, and reducing costs.
Response: The definition of a visit for purposes of Medicare home
health services as set forth in Sec. 409.48(c) specifies that a visit
is an episode of personal contact with the beneficiary by
[[Page 51695]]
staff of the HHA or others under arrangements with the HHA for the
purpose of providing a covered service. A telephone contact or
telehealth visit does not meet the definition of a visit and therefore
does not count as a visit. While there is nothing to preclude an HHA
from furnishing services via telehealth or other technologies that they
believe promote efficiencies, those technologies are not specifically
recognized and paid by Medicare under the home health benefit.
Comment: Several commenters expressed concerns with the wage index
for rural areas in Maine, citing it as one of the lowest in New
England. Another commenter questioned the validity of the wage index
data, especially in the case of the CBSA for Albany-Schenectady-Troy,
noting that in the past 5 years, this CBSA has seen its wage index
reduced 5.41 percent, going from 0.8647 in 2013 to a proposed CY 2018
wage index of 0.8179.
Response: As discussed in the CY 2017 HH PPS final rule (81 FR
76721), we believe that the wage index values are reflective of the
labor costs in each geographic area as they reflect the costs included
on the cost reports of hospitals in those specific labor market areas.
The wage index values are based on data submitted on the inpatient
hospital cost reports. We utilize efficient means to ensure and review
the accuracy of the hospital cost report data and resulting wage index.
The home health wage index is derived from the pre-floor, pre-
reclassified wage index, which is calculated based on cost report data
from hospitals paid under the Hospital Inpatient Prospective Payment
System (IPPS). All IPPS hospitals must complete the wage index survey
(Worksheet S-3, Parts II and III) as part of their Medicare cost
reports. Cost reports will be rejected if Worksheet S- 3 is not
completed. In addition, Medicare contractors perform desk reviews on
all hospitals' Worksheet S-3 wage data, and we run edits on the wage
data to further ensure the accuracy and validity of the wage data. We
believe that our review processes result in an accurate reflection of
the applicable wages for the areas given. The processes and procedures
describing how the inpatient hospital wage index is developed are
discussed in the IPPS rule each year, with the most recent discussion
provided in the FY 2018 IPPS final rule (82 FR 38130 through 38136 and
82 FR 38152 through 38156). Any provider type may submit comments on
the hospital wage index during the annual IPPS rulemaking cycle.
Comment: A commenter stated that CMS's decision to switch from MSAs
to the CBSAs for the wage index calculation has had serious financial
ramifications for New York HHAs. The commenter stated that CMS's shift
to the CBSA wage index designation has resulted in below trend
reimbursement for New York City agencies.
Response: The MSA delineations as well as the CBSA delineations are
determined by the OMB. The OMB reviews its Metropolitan Area
definitions preceding each decennial census to reflect recent
population changes. We believe that the OMB's CBSA designations reflect
the most recent available geographic classifications and are a
reasonable and appropriate way to define geographic areas for purposes
of wage index values.
Comment: Several commenters opposed the fact that hospitals are
given the opportunity to appeal their annual wage index and apply for
geographic reclassification while HHAs in the same geographic location
are not given that same privilege. The commenters believe that this
lack of parity between different health care sectors further
exemplifies the inadequacy of CMS's decision to continue to use the
pre-floor, pre-reclassified hospital wage index to adjust home health
services payment rates. Another commenter suggests that CMS include
wage data from reclassified hospitals in calculating rural wage index
values.
Response: We continue to believe that the regulations and statutes
that govern the HH PPS do not provide a mechanism for allowing HHAs to
seek geographic reclassification or to utilize the rural floor
provisions that exist for IPPS hospitals. Section 4410(a) of the BBA
provides that the area wage index applicable to any hospital that is
located in an urban area of a State may not be less than the area wage
index applicable to hospitals located in rural areas in that state.
This is the rural floor provision and it is specific to hospitals. The
reclassification provision at section 1886(d)(10)(C)(i) of the Act
states that the Board shall consider the application of any subsection
(d) hospital requesting the Secretary change the hospital's geographic
classification. This reclassification provision is only applicable to
hospitals as defined in section 1886(d) of the Act. In addition, we do
not believe that using hospital reclassification data would be
appropriate as these data are specific to the requesting hospitals and
may or may not apply to a given HHA.
We continue to believe that using the pre-floor, pre-reclassified
hospital wage index as the wage adjustment to the labor portion of the
HH PPS rates is appropriate and reasonable.
Comment: Several commenters requested that CMS explore wholesale
revision and reform of the home health wage index, including the
development of a home health-specific wage index. Commenters noted that
reform of the home health wage index should address the commenters'
following concerns and opinions: (1) The impact on care access and
financial stability of HHAs at the local level; (2) the unpredictable
year-to-year swings in wage index values that are often based on
inaccurate or incomplete hospital cost reports which have negatively
impacted HHAs throughout the years and jeopardized access to care; (3)
the inadequacy and inaccuracy of the pre-floor, pre-reclassified
hospital wage index for adjusting home health costs; and (4) the labor
market distortions created by reclassification of hospitals in areas in
which home health labor costs are not reclassified.
Response: We appreciate the commenter's recommendation to continue
exploring potential approaches for wage index reform, including
collecting home health-specific wage data in order to establish a home
health-specific wage index. We note that our previous attempts at
either proposing or developing a home health-specific wage index were
not well-received by the home health industry. In September 30, 1988
Federal Register notice (53 FR 38476), the Health Care Financing
Administration (HCFA), as CMS was then known, implemented an HHA-
specific wage index based on data received from HHAs. Subsequently,
providers gave significant feedback concerning the burden that the
reporting requirements posed and the accuracy of the data. As a result,
the Medicare Catastrophic Coverage Act of 1988 retroactively repealed
the use of an HHA-specific wage index and referenced use of the
hospital wage index (see section 1895(b)(4)(C) of the Act). While this
occurred many years ago, we believe that HHAs would voice similar
concerns regarding the burden such reporting requirements would place
on HHAs.
Consistent with our previous responses to these recurring comments
(most recently published in the CY 2016 HH PPS final rule (80 FR
68654)), we also note that developing such a wage index would require a
resource-intensive audit process similar to that used for IPPS hospital
data, to improve the quality of the HHA cost report data in order for
it to be used as part of this analysis. This audit process is quite
extensive in the case of approximately
[[Page 51696]]
3,300 hospitals, it would be significantly more so in the case of
approximately 11,000 HHAs. We believe auditing all HHA cost reports,
similar to the process used to audit inpatient hospital cost reports
for purposes of the IPPS wage index, would also place a burden on
providers in terms of recordkeeping and completion of the cost report
worksheet.
We also believe that adopting such an approach would require a
significant commitment of resources by CMS and the Medicare
Administrative Contractors, potentially far in excess of those required
under the IPPS given that there are more than three times as many HHAs
as there are hospitals. Therefore, we continue to believe that, in the
absence of the appropriate home health-specific wage data, using the
pre-floor, pre-reclassified inpatient hospital wage data is appropriate
and reasonable for the HH PPS.
Finally, CMS has conducted research on a possible alternative to
the hospital wage index. CMS issued its ``Report to Congress: Plan to
Reform the Medicare Wage Index'' concerning the hospital wage index, on
April 11, 2012 and is available on our Wage Index Reform Web page
https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/AcuteInpatientPPS/Wage-Index-Reform.html. This report describes the
concept of a commuting-based wage index (CBWI). However, implementation
of a CBWI may require both statutory and regulatory changes. In
addition, we believe other intermediate steps for implementation,
including the collection of commuting data, may be necessary. In
considering alternative methodologies for area wage adjustment, CMS
would have to consider whether the benefits of such methodologies
outweigh the reporting, record keeping and audit burden that would be
placed on HHAs and/or other providers.
Comment: Several commenters stated that the pre-floor, pre-
reclassified hospital wage index is inadequate for adjusting home
health costs, particularly in states like New York, which has among the
nation's highest labor costs, exacerbated, in the commenters' opinions,
by their state's implementation of a phased-in $15 per-hour minimum
wage hike, which they argue would be unfunded by Medicare. The
commenters estimated that the minimum wage mandate, when fully phased-
in, would add $2 billion in costs for that state's HHAs across all
payers (Medicaid, Medicare, managed care, commercial insurance and
private-pay), and would not be captured by the pre-floor, pre-
reclassified hospital wage index. One commenter recommended that
providers meeting higher minimum wage standards, such as HHAs, obtain
additional supplemental funding to better align payments with cost
trends impacting providers.
Response: Regarding minimum wage standards, we note that such
increases will be reflected in future data used to create the hospital
wage index to the extent that these changes to state minimum wage
standards are reflected in increased wages to hospital staff.
Comment: Commenters raised issues with CMS's decision to maintain
the current policy of using the pre-floor, pre-reclassified hospital
wage index to adjust home health services payment rates because this
resulted in volatility in the home health wage index from one year to
the next. These commenters believe that what they view as unpredictable
year-to-year swings in wage index values were based on inaccurate or
incomplete hospital cost reports.
Response: We appreciate the commenters' concerns regarding the
accuracy of the home health wage index. We utilize efficient means to
ensure and review the accuracy of the hospital cost report data and
resulting wage index. The home health wage index is derived from the
pre-floor, pre-reclassified wage index, which is calculated based on
cost report data from hospitals paid under the IPPS. All IPPS hospitals
must complete the wage index survey (Worksheet S-3, Parts II and III)
as part of their Medicare cost reports. Cost reports will be rejected
if Worksheet S-3 is not completed. In addition, Medicare contractors
perform desk reviews on all hospitals' Worksheet S-3 wage data, and we
run edits on the wage data to further ensure the accuracy and validity
of the wage data. We believe that our review processes result in an
accurate reflection of the applicable wages for the areas given. The
processes and procedures describing how the inpatient hospital wage
index is developed, including a wage data verification and correction
process, are discussed in the IPPS rule each year, with the most recent
discussion provided in the FY 2018 IPPS final rule (82 FR 38130 through
38136, and 82 FR 38152 through 38156). Any provider type may submit
comments on the hospital wage index during the annual IPPS rulemaking
cycle.
Comment: A commenter recommended that CMS research the impact of
instituting a population density adjustment to the labor portion of the
HH PPS payments.
Response: As discussed in the CY 2017 HH PPS final rule (81 FR
76721), we do not believe that a population density adjustment is
appropriate at this time. Rural HHAs continually cite the added cost of
traveling from one patient to the next patient. However, urban HHAs
cite the added costs associated with needed security measures and
traffic congestion. The home health wage index values in rural areas
are not necessarily lower than the home health wage index values in
urban areas. The home health wage index reflects the wages that
inpatient hospitals pay in their local geographic areas.
Final Decision: After considering the comments received in response
to the CY 2018 HH PPS proposed rule, we are finalizing our proposal to
use the pre-floor, pre-reclassified hospital inpatient wage index as
the wage adjustment to the labor portion of the HH PPS rates. For CY
2018, the updated wage data are for the hospital cost reporting periods
beginning on or after October 1, 2013 and before October 1, 2014 (FY
2014 cost report data). In addition, we are implementing the third and
final year of a 0.97 percent payment reduction to account for nominal
case-mix growth from CY 2012 through CY 2014 when finalizing the CY
2018 HH PPS payment rates. We note that the payment reductions to
account for nominal case-mix growth from 2012 to 2014 were finalized in
the CY 2016 HH PPS final rule. No additional adjustments or reductions
were proposed in the CY 2018 proposed rule.
D. Payments for High-Cost Outliers Under the HH PPS
1. Background
Section 1895(b)(5) of the Act allows for the provision of an
addition or adjustment to the home health payment amount in the case of
outliers because of unusual variations in the type or amount of
medically necessary care. Outlier payments serve as a type of
``reinsurance'' whereby, under the HH PPS, Medicare reimburses HHAs 80
percent of their costs for outlier cases once the case exceeds an
outlier threshold amount. Prior to the enactment of the Affordable Care
Act, section 1895(b)(5) of the Act stipulated that projected total
outlier payments could not exceed 5 percent of total projected or
estimated HH payments in a given year. In the July 3, 2000 Medicare
Program; Prospective Payment System for Home Health Agencies final rule
(65 FR 41188 through 41190), we described the method for determining
outlier payments. Under this system, outlier payments are made for
episodes
[[Page 51697]]
whose estimated costs exceed a threshold amount for each Home Health
Resource Group (HHRG). The episode's estimated cost was established as
the sum of the national wage-adjusted per-visit payment amounts
delivered during the episode. The outlier threshold for each case-mix
group or Partial Episode Payment (PEP) adjustment is defined as the 60-
day episode payment or PEP adjustment for that group plus a fixed-
dollar loss (FDL) amount. The outlier payment is defined to be a
proportion of the wage-adjusted estimated cost beyond the wage-adjusted
threshold. The threshold amount is the sum of the wage and case-mix
adjusted PPS episode amount and wage-adjusted FDL amount. The
proportion of additional costs over the outlier threshold amount paid
as outlier payments is referred to as the loss-sharing ratio.
In the CY 2010 HH PPS proposed rule (74 FR 40948, 40957), we stated
that outlier payments increased as a percentage of total payments from
4.1 percent in CY 2005, to 5.0 percent in CY 2006, to 6.4 percent in CY
2007 and that this excessive growth in outlier payments was primarily
the result of unusually high outlier payments in a few areas of the
country. In that discussion, we noted that despite program integrity
efforts associated with excessive outlier payments in targeted areas of
the country, we discovered that outlier expenditures still exceeded the
5 percent target in CY 2007 and, in the absence of corrective measures,
would continue do to so. Consequently, we assessed the appropriateness
of taking action to curb outlier abuse. As described in the CY 2010 HH
PPS final rule (74 FR 58080 through 58087), to mitigate possible
billing vulnerabilities associated with excessive outlier payments and
adhere to our statutory limit on outlier payments, we finalized an
outlier policy that included a 10 percent agency-level cap on outlier
payments. This cap was implemented in concert with a reduced FDL ratio
of 0.67. These policies resulted in a projected target outlier pool of
approximately 2.5 percent. (The previous outlier pool was 5 percent of
total home health expenditures). For CY 2010, we first returned the 5
percent held for the previous target outlier pool to the national,
standardized 60-day episode rates, the national per-visit rates, the
LUPA add-on payment amount, and the NRS conversion factor. Then, we
reduced the CY 2010 rates by 2.5 percent to account for the new outlier
pool of 2.5 percent. This outlier policy was adopted for CY 2010 only.
As we noted in the CY 2011 HH PPS final rule (75 FR 70397 through
70399), section 3131(b)(1) of the Affordable Care Act amended section
1895(b)(3)(C) of the Act, and required the Secretary to reduce the HH
PPS payment rates such that aggregate HH PPS payments were reduced by 5
percent. In addition, section 3131(b)(2) of the Affordable Care Act
amended section 1895(b)(5) of the Act by redesignating the existing
language as section 1895(b)(5)(A) of the Act, and revising the language
to state that the total amount of the additional payments or payment
adjustments for outlier episodes may not exceed 2.5 percent of the
estimated total HH PPS payments for that year. Section 3131(b)(2)(C) of
the Affordable Care Act also added section 1895(b)(5)(B) of the Act
which capped outlier payments as a percent of total payments for each
HHA at 10 percent.
As such, beginning in CY 2011, our HH PPS outlier policy is that we
reduce payment rates by 5 percent and target up to 2.5 percent of total
estimated HH PPS payments to be paid as outliers. To do so, we returned
the 2.5 percent held for the target CY 2010 outlier pool to the
national, standardized 60-day episode rates, the national per visit
rates, the LUPA add-on payment amount, and the NRS conversion factor
for CY 2010. Then we reduced the rates by 5 percent as required by
section 1895(b)(3)(C) of the Act, as amended by section 3131(b)(1) of
the Affordable Care Act. For CY 2011 and subsequent calendar years we
target up to 2.5 percent of estimated total payments to be paid as
outlier payments, and apply a 10 percent agency-level outlier cap.
In the CY 2017 HH PPS proposed and final rules (81 FR 43737 through
43742 and 81 FR 76724), we described our concerns regarding patterns
observed in home health outlier episodes. Specifically, we noted that
the methodology for calculating home health outlier payments may have
created a financial incentive for providers to increase the number of
visits during an episode of care to surpass the outlier threshold and
simultaneously created a disincentive for providers to treat medically
complex beneficiaries who require fewer but longer visits. Given these
concerns, in the CY 2017 HH PPS final rule (81 FR 76724), we finalized
changes to the methodology used to calculate outlier payments, using a
cost-per-unit approach rather than a cost-per-visit approach. This
change in methodology allows for more accurate payment for outlier
episodes, accounting for both the number of visits during an episode of
care and also the length of the visits provided. Using this approach,
we now convert the national per-visit rates into per 15-minute unit
rates. These per 15-minute unit rates are used to calculate the
estimated cost of an episode to determine whether the claim will
receive an outlier payment and the amount of payment for an episode of
care. In conjunction with our finalized policy to change to a cost-per-
unit approach to estimate episode costs and determine whether an
outlier episode should receive outlier payments, in the CY 2017 HH PPS
final rule (81 FR 76725) we also finalized the implementation of a cap
on the amount of time per day that would be counted toward the
estimation of an episode's costs for outlier calculation purposes.
Specifically, we limit the amount of time per day (summed across the
six disciplines of care) to 8 hours (32 units) per day when estimating
the cost of an episode for outlier calculation purposes.
2. Fixed Dollar Loss (FDL) Ratio
For a given level of outlier payments, there is a trade-off between
the values selected for the FDL ratio and the loss-sharing ratio. A
high FDL ratio reduces the number of episodes that can receive outlier
payments, but makes it possible to select a higher loss-sharing ratio,
and therefore, increase outlier payments for qualifying outlier
episodes. Alternatively, a lower FDL ratio means that more episodes can
qualify for outlier payments, but outlier payments per episode must
then be lower.
The FDL ratio and the loss-sharing ratio must be selected so that
the estimated total outlier payments do not exceed the 2.5 percent
aggregate level (as required by section 1895(b)(5)(A) of the Act).
Historically, we have used a value of 0.80 for the loss-sharing ratio
which, we believe, preserves incentives for agencies to attempt to
provide care efficiently for outlier cases. With a loss-sharing ratio
of 0.80, Medicare pays 80 percent of the additional estimated costs
above the outlier threshold amount.
Simulations based on CY 2015 claims data (as of June 30, 2016)
completed for the CY 2017 HH PPS final rule showed that outlier
payments were estimated to represent approximately 2.84 percent of
total HH PPS payments in CY 2017, and as such, we finalized a change to
the FDL ratio from 0.45 to 0.55. We stated that raising the FDL ratio
to 0.55, while maintaining a loss-sharing ratio of 0.80, struck an
effective balance of compensating for high-cost episodes while still
meeting the statutory requirement to target up to, but no more than,
2.5 percent of total payments as outlier payments (81 FR 76726). The
national, standardized 60-day episode payment amount is multiplied by
the FDL ratio. That amount is wage-adjusted
[[Page 51698]]
to derive the wage-adjusted FDL amount, which is added to the case-mix
and wage-adjusted 60-day episode payment amount to determine the
outlier threshold amount that costs have to exceed before Medicare
would pay 80 percent of the additional estimated costs.
Using preliminary CY 2016 claims data (as of March 17, 2017) and
the proposed CY 2018 payment rates presented in section III.C. of the
CY 2018 HH PPS proposed rule (82 FR 35293), we estimated that outlier
payments would constitute approximately 2.47 percent of total HH PPS
payments in CY 2018 under the current outlier methodology. Given the
statutory requirement to target up to, but no more than, 2.5 percent of
total payments as outlier payments, we did not propose a change to the
FDL ratio for CY 2018 as we believed that maintaining an FDL ratio of
0.55 with a loss-sharing ratio of 0.80 was still appropriate given the
percentage of outlier payments projected for CY 2018. Likewise, we did
not propose a change to the loss-sharing ratio (0.80) for the HH PPS to
remain consistent with payment for high-cost outliers in other Medicare
payment systems (for example, Inpatient Rehabilitation Facility (IRF)
PPS, IPPS, etc.). While we did not propose to change the FDL ratio of
0.55 for CY 2018, we noted that we would update our estimate of outlier
payments as a percent of total HH PPS payments using the most current
and complete year of HH PPS data (CY 2016 claims data as of June 30,
2017 or later) in this final rule.
Using updated CY 2016 claims data (as of August 18, 2017) and the
final CY 2018 payment rates presented in section III.C of this final
rule, we estimate that outlier payments would continue to constitute
approximately 2.47 percent of total HH PPS payments in CY 2018 under
the current outlier methodology. Given the statutory requirement to
target up to, but no more than, 2.5 percent of total payments as
outlier payments, we continue to believe that maintaining an FDL ratio
of 0.55 with a loss-sharing ratio of 0.80 is still appropriate given
the percentage of outlier payments projected for CY 2018.
The following is a summary of the comments received and our
responses.
Comment: A commenter questioned if we would provide the CY 2018
cost-per-unit values to be used for the outlier calculation.
Response: The cost-per-unit amounts for CY 2018 are in Table 14 of
this final rule. We note that in the CY 2017 HH PPS final rule (81 FR
76724), we stated that we did not plan to re-estimate the average
minutes per visit by discipline every year. Additionally, we noted that
the per-unit rates used to estimate an episode's cost will be updated
by the home health update percentage each year, meaning we would start
with the national per-visit amounts for the same calendar year when
calculating the cost-per-unit used to determine the cost of an episode
of care (81 FR 76727).
Table 14--CY 2018 Cost-Per-Unit Payment Rates for the Calculation of Outlier Payments *
----------------------------------------------------------------------------------------------------------------
CY 2018
National per- Average Cost-per-unit
Visit type visit payment minutes- per- (1 unit = 15
rates visit minutes)
----------------------------------------------------------------------------------------------------------------
Home health aide................................................ $64.94 63.0 $15.46
Medical social services......................................... 229.86 56.5 61.02
Occupational therapy............................................ 157.83 47.1 50.26
Physical therapy................................................ 156.76 46.6 50.46
Skilled nursing................................................. 143.40 44.8 48.01
Speech-language pathology....................................... 170.38 48.1 53.13
----------------------------------------------------------------------------------------------------------------
* These values reflect the national per visit rates for each discipline for providers who have submitted quality
data; for rates applicable to those providers who did not submit quality data submitted, please see our
forthcoming CY 2018 Rate Update Change Request, which will be available here: https://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/2017-Transmittals.html.
We note that we will continue to monitor the visit length by
discipline as more recent data become available, and we may propose to
update the rates as needed in the future.
Comment: Several commenters stated that the changes to the outlier
methodology made in the CY 2017 final rule, particularly the increase
in the FDL ratio from 0.45 to 0.55, were significant and may have led
to a reduction in the number of home health episodes that would qualify
for outlier payment. The commenters recommended that CMS release data
on the impact of this policy change on the dually eligible beneficiary
population and in particular those patients with clinically complex
conditions.
Response: We appreciate the commenters' concerns regarding the
potential impact of the changes to the outlier policy finalized in the
CY 2017 HH PPS final rule (81 FR 76727). Data reflecting the changes to
the outlier policy made for CY 2017 are not yet available for analysis
and assessment. However, as these updated data become available, we
will evaluate for changes, analyze patterns in home health outlier
payments, and monitor for any impacts, particularly for those
beneficiaries with clinically complex conditions, and may include the
results of such efforts in future rulemaking.
Additionally, as discussed in the CY 2017 HH PPS final rule (81 FR
76728), the goal of this policy change is to more accurately pay for
outlier episodes. We noted in the CY 2017 HH PPS proposed rule that
analysis indicates that a larger percentage of episodes of care for
patients with a fragile overall health status will qualify for outlier
payments (81 FR 43713). The outlier system is meant to help address
extra costs associated with extra, and potentially unpredictable,
medically necessary care. In section II.D. of the CY 2018 HH PPS
proposed rule (82 FR 35275), we discussed Report to Congress: Home
Health Study on Access to Care for Vulnerable Patient Populations and
Subsequent Research and Analyses. We believe that this change in the
outlier payment policy may ultimately serve to address some of the
findings from the home health study, where margins were lower for
patients with medically complex needs that typically require longer
visits, thus potentially creating an incentive to treat only or
primarily patients with less complex needs.
Moreover, the 2.5 percent target of outlier payments to total home
health payments is a statutory requirement, as established in section
1895(b)(5) of the Act. Therefore, we modified the FDL in order to align
the estimated outlier payments with the 2.5 percent target required by
law.
[[Page 51699]]
Comment: A few commenters expressed disagreement with CMS's
decision to maintain the existing 10-percent cap on outlier payments to
HHAs as a purported fraud-fighting effort, suggesting that a
potentially more appropriate and targeted fraud-fighting initiative
will include a possible minimum provider-specific number or percent of
episodes that result in LUPAs, suggesting that reporting periods with
zero LUPAs could be an indicator of inappropriate provider behavior.
Response: Regarding the appropriateness of the 10 percent per-
agency cap, we note that the 2.5 percent target of outlier payments to
total home health payments and the 10 percent cap on outlier payments
at the home health agency level are statutory requirements, as
established in section 1895(b)(5) of the Act. Therefore, we do not have
the authority to adjust or eliminate the 10-percent cap or increase the
2.5 percent target amount. Additionally, we appreciate the commenter's
suggestion regarding alternative approaches for targeting fraud within
the Medicare home health benefit. The Program for Evaluating Payment
Patterns Electronic Report (PEPPER) is a comparative data report that
summarizes a single provider's Medicare claims data statistics for
services vulnerable to improper payments. PEPPER can support a hospital
or facility's compliance efforts by identifying where its billing
patterns are different from the majority of other providers in the
nation. This data can help identify both potential overpayments and
potential underpayments, and can provide guidance on areas in which a
provider may want to focus auditing and monitoring efforts with the
goal of preventing improper Medicare payments. In the HHA PEPPER, we
include a metric for non-LUPA payment, which represents the count of
episodes paid to the HHA that did not have a LUPA payment during the
report period as a proportion of total episodes paid to the HHA during
the report period (available at: https://www.pepperresources.org/Portals/0/Documents/PEPPER/HHA/HHA_PEPPERUsersGuide_Edition2.pdf). This
measure is provided to the HHA community for review and may also be
used by our Center for Program Integrity as a guide for audits and
other investigative efforts.
We also note that, as described in the CY 2017 HH PPS final rule
(82 FR 76727), in 2015, only about 1 percent of HHAs received 10
percent of their total HH PPS payments as outlier payments, while
almost 71 percent of HHAs received less than 1 percent of their total
HH PPS payments as outliers. Therefore, the 10 percent agency-level cap
does not seem to significantly impact a large portion of HHAs.
Comment: Several commenters recommended that CMS conduct a more
detailed analysis to determine whether the total cap of 2.5 percent of
total payments as outlier payments is adequate or whether it needs to
be increased for future years, particularly given the expected change
in Medicare beneficiary demographics anticipated in the coming years.
Response: As established in section 1895(b)(5) of the Act, both the
2.5 percent target of outlier payments to total home health payments
and the 10-percent cap on outlier payments at the home health agency
level are statutory requirements. Therefore, we do not have the
authority to adjust or eliminate the 10-percent cap or increase the
2.5-percent target amount. However, we will continue to evaluate for
the appropriateness of those elements of the outlier policy that may be
modified, including the FDL and the loss-sharing ratio. We note that
other Medicare payment systems with outlier payments, such as the IRF
PPS and IPPS, annually reassess the fixed-loss cost outlier threshold
amount. Adjusting the outlier threshold amount in order to target the
statutorily required percentage of total payments as outlier payments
is standard practice.
Comment: A commenter recommended that CMS eliminate outlier
payments in their entirety.
Response: We believe that section 1895(b)(5)(A) of the Act allows
the Secretary the discretion as to whether or not to have an outlier
policy under the HH PPS. However, we also believe that outlier payments
are beneficial in that they help mitigate the incentive for HHAs to
avoid patients that may have episodes of care that result in unusual
variations in the type or amount of medically necessary care. The
outlier system is meant to help address extra costs associated with
extra, and potentially unpredictable, medically necessary care. We note
that we plan to continue evaluating whether or not an outlier policy
remains appropriate as well as ways to maintain an outlier policy for
episodes that incur unusually high costs due to patient care needs.
Final Decision: We are finalizing no change to the FDL ratio or
loss sharing ratio for CY 2018. We are maintaining an FDL ratio of 0.55
with a loss-sharing ratio of 0.80 for CY 2018. However, we will
continue to monitor outlier payments and continue to explore ways to
maintain an outlier policy for episodes that incur unusually high
costs.
E. Proposed Implementation of the Home Health Groupings Model (HHGM)
for CY 2019
We proposed case-mix methodology refinements through the
implementation of the Home Health Groupings Model (HHGM). We proposed
to implement the HHGM for home health periods of care beginning on or
after January 1, 2019. The HHGM uses 30-day periods rather than the 60-
day episode used in the current payment system, eliminates the use of
the number of therapy visits provided to determine payment, and relies
more heavily on clinical characteristics and other patient information
(for example, diagnosis, functional level, comorbid conditions,
admission source) to place patients into clinically meaningful payment
categories.
We are not finalizing the implementation of the HHGM in this final
rule. We received many comments from the public that we would like to
take into further consideration. While commenters were generally
supportive of the concept of revising the HH PPS case-mix methodology
to better align payments with the costs of providing care, commenters
included technical comments on various aspects of the proposed case-mix
adjustment methodology under the HHGM and were most concerned about the
proposed change in the unit of payment from 60 days to 30 days and such
change being proposed for implementation in a non-budget neutral
manner. Commenters also stated their desire for greater involvement in
the development of the HHGM and the need for access to the necessary
data in order to replicate and model the effects on their businesses.
We note that information continues to be available to stakeholders
around this important initiative. The analyses and the ultimate
development of HHGM was previously shared with both internal and
external stakeholders via technical expert panels, clinical workgroups,
and special open door forums. We provided high-level summaries on our
case-mix methodology refinement work in the HH PPS proposed rules for
CYs 2016 and 2017 (80 FR 39839, and 81 FR 76702). Additionally, a
detailed technical report was posted on the CMS Web site in December
2016 and remains available, additional technical expert panel and
clinical workgroup webinars were held after the posting of the
technical report, and a National Provider call occurred in January 2017
to further solicit feedback from stakeholders and the general
[[Page 51700]]
public.\12\ As many did, any provider or organization wishing to
receive the necessary data to replicate and model the effects of the
HHGM or study the Medicare home health benefit can submit a request
through the CMS Data Request Center.\13\ We note that the Home Health
Agency Limited Data Set files and Research Identifiable Files are
available on a quarterly and annual basis. The fourth quarter data for
CY 2016 were available in mid-May of 2017. The fourth quarter files
include all final action fee-for-service claims received by December
31, 2016. We also posted a HHGM Groupings Tool along with the CY 2018
HH PPS proposed rule on the HHA Center Web page, which providers can
continue to use in order to replicate the HHGM methodology using their
own internal data.
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\12\ https://www.cms.gov/Outreach-and-Education/Outreach/NPC/National-Provider-Calls-and-Events-Items/2017-01-18-Home-Health.html.
\13\ https://www.resdac.org/cms-data/request/cms-data-request-center.
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We also note that, in the CY 2018 HH PPS proposed rule, we assumed
that behavioral responses would occur upon implementation of the HHGM.
If no behavioral assumptions were made and we implemented the HHGM for
CY 2018, we estimate that the 30-day payment amount needed to achieve
budget neutrality would have been $1,722.29. However, because we have a
continued fiduciary duty as stewards of the Medicare program to
mitigate potential overpayments, if possible, we assumed behavioral
responses would occur in the estimation of the 30-day payment amount.
We determined that, if the HHGM were implemented for CY 2018 with
assumed behavioral responses, the 30-day payment amount needed to
achieve budget neutrality would have been $1,622.61. For the CY 2018 HH
PPS proposed rule, we included two behavioral assumptions in our impact
estimates related to the proposed implementation of the HHGM for CY
2019: (1) For LUPAs one visit under the proposed HHGM case-mix group
thresholds, HHAs would provide an additional visit so the 30-day period
of care becomes a non-LUPA; and (2) the highest-paying diagnosis code
would be listed as primary for clinical grouping assignment. While we
do not support or condone coding practices or the provision of services
solely to maximize payment, we often take into account expected
behavioral effects of policy changes related to rate setting. We
included a LUPA behavioral assumption in our estimated impact of the
HHGM based on past behavioral assumptions made under the HH PPS. As
noted in the FY 2001 HH PPS final rule, the episode file showed that
approximately 16 percent of episodes would have received a LUPA (65 FR
41162). However, currently, about 7 percent of all 60-day episodes
receive a LUPA. For the HHGM, approximately 7 percent of 30-day periods
would receive a LUPA. However, because 4.9 percent of 30-day periods of
care are just one visit below the LUPA thresholds under the HHGM, we
assume that for these 30-day periods, HHAs will provide an additional
visit to avoid receiving a LUPA, especially in the absence of therapy
thresholds and the change from a 60-day to 30-day unit of payment.
With regards to our assumption that HHAs would code the highest-
paying diagnosis code as primary for the clinical grouping assignment,
this assumption was based on decades of past experience under the HH
PPS and other case-mix systems, such as the implementation of the
diagnosis-related groups (DRGs) and the Medicare Severity (MS)-DRGs
under the inpatient prospective payment system. In the FY 2008 IPPS
final rule (72 FR 47176), we noted that case-mix refinements can lead
to substantial unwarranted increase in payments. To address this issue
when CMS transitioned from DRGs to MS-DRGs, MedPAC recommended that the
Secretary project the likely effect of reporting improvements on total
payments and make an offsetting adjustment to the national average base
payment amounts (72 FR 47176). In the FY 2008 IPPS final rule (72 FR
47181), we summarized instances where case-mix increases resulted from
documentation and coding-induced changes for the first year of the IRF
PPS and in Maryland hospitals' transition to APR DRGs (estimated at
around 5 percent in both instances). Therefore, we estimated that an
adjustment of 4.8 percent would be necessary to maintain budget
neutrality for the transition to the MS-DRGs (72 FR 47178). With
regards to experience under the HH PPS, as outlined in the CY 2018 HH
PPS proposed rule (82 FR 35274), between CY 2000 and 2010, total case-
mix change was 23.90 percent, with 20.08 considered nominal case-mix
growth, an average of approximately 2 percent nominal case-mix growth
per year.
IV. Provisions of the Home Health Value-Based Purchasing (HHVBP) Model
A. Background
As authorized by section 1115A of the Act and finalized in the CY
2016 HH PPS final rule (80 FR 68624), we began testing the HHVBP Model
on January 1, 2016. The HHVBP Model has an overall purpose of improving
the quality and delivery of home health care services to Medicare
beneficiaries. The specific goals of the Model are to: (1) Provide
incentives for better quality care with greater efficiency; (2) study
new potential quality and efficiency measures for appropriateness in
the home health setting; and (3) enhance the current public reporting
process.
Using the randomized selection methodology finalized in the CY 2016
HH PPS final rule, nine states were selected for inclusion in the HHVBP
Model, representing each geographic area across the nation. All
Medicare-certified HHAs providing services in Arizona, Florida, Iowa,
Maryland, Massachusetts, Nebraska, North Carolina, Tennessee, and
Washington (competing HHAs) are required to compete in the Model.
Requiring all Medicare-certified HHAs providing services in the
selected states to participate in the Model ensures that: (1) There is
no selection bias; (2) participating HHAs are representative of HHAs
nationally; and, (3) there is sufficient participation to generate
meaningful results.
As finalized in the CY 2016 HH PPS final rule, the HHVBP Model will
utilize the waiver authority under section 1115A(d)(1) of the Act to
adjust Medicare payment rates under section 1895(b) of the Act
beginning in CY 2018 based on performance on applicable measures.
Payment adjustments will be increased incrementally over the course of
the HHVBP Model in the following manner: (1) A maximum payment
adjustment of 3 percent (upward or downward) in CY 2018; (2) a maximum
payment adjustment of 5 percent (upward or downward) in CY 2019; (3) a
maximum payment adjustment of 6 percent (upward or downward) in CY
2020; (4) a maximum payment adjustment of 7 percent (upward or
downward) in CY 2021; and (5) a maximum payment adjustment of 8 percent
(upward or downward) in CY 2022. Payment adjustments will be based on
each HHA's Total Performance Score (TPS) in a given performance year
(PY) on: (1) A set of measures already reported via OASIS and HHCAHPS
for all patients serviced by the HHA and select claims data elements;
and (2) three new measures where points are achieved for reporting
data.
In the CY 2017 HH PPS final rule (81 FR 76741 through 76752), in
addition to providing an update on the progress towards developing
public reporting of performance under the HHVBP Model, we finalized the
following changes related to the HHVBP Model:
[[Page 51701]]
Calculating benchmarks and achievement thresholds at the
state level rather than the level of the size-cohort and revising the
definition for benchmark to state that benchmark refers to the mean of
the top decile of Medicare-certified HHA performance on the specified
quality measure during the baseline period, calculated for each state.
Requiring a minimum of eight HHAs in a size-cohort.
Increasing the timeframe for submitting new measure data
from seven calendar days to 15 calendar days following the end of each
reporting period to account for weekends and holidays.
Removing four measures (Care Management: Types and Sources
of Assistance, Prior Functioning Activities of Daily Living (ADL)/
Instrumental ADL (IADL), Influenza Vaccine Data Collection Period, and
Reason Pneumococcal Vaccine Not Received) from the set of applicable
measures.
Adjusting the reporting period and submission date for the
Influenza Vaccination Coverage for Home Health Personnel measure from a
quarterly submission to an annual submission.
Allowing for an appeals process that includes the
recalculation process finalized in the CY 2016 HH PPS final rule (80 FR
68688 through 68689), as modified, and adds a reconsideration process.
B. Quality Measures
1. Adjustment to the Minimum Number of Completed Home Health Care
Consumer Assessment of Healthcare Providers and System (HHCAHPS)
Surveys
The HHCAHPS survey presents home health patients with a set of
standardized questions about their home health care providers and about
the quality of their home health care. The survey is designed to
measure the experiences of people receiving home health care from
Medicare-certified home health care agencies and meet the following
three broad goals to: (1) Produce comparable data on the patient's
perspective that allows objective and meaningful comparisons between
HHAs on domains that are important to consumers; (2) create incentives
through public reporting of survey results for agencies to improve
their quality of care; and (3) enhance public accountability in health
care by increasing the transparency of the quality of care provided in
return for public investment through public reporting.
As finalized in the CY 2016 HH PPS final rule (80 FR 68685 through
68686), if a HHA does not have a minimum of 20 episodes of care during
a performance year (PY) to generate a performance score on at least
five measures, that HHA would not be included in the Linear Exchange
Function (LEF) and would not have a payment adjustment percentage
calculated. The LEF is used to translate an HHA's Total Performance
Score (TPS) into a percentage of the value-based payment adjustment
earned by each HHA under the HHVBP Model. For the HHCAHPS measures, a
minimum of 20 HHCAHPS completed surveys would be necessary in order for
scores to be generated for the HHCAHPS quality measures that can be
included in the calculation of the TPS.
However, as we stated in the CY 2018 HH PPS proposed rule (82 FR
35333), we believe that using a minimum of 40 completed HHCAHPS
surveys, rather than a minimum of 20 completed HHCAHPS surveys, will
better align the Model with HHCAHPS policy for the Patient Survey Star
Ratings on Home Health Compare.\14\ The decision to use a minimum of 40
completed surveys for these star ratings was a result of balancing two
competing goals. One goal was to provide star ratings that were
meaningful and minimized random variations. This goal was best served
by calculating star ratings for large numbers of cases by having a
larger minimum of completed HHCAHPS surveys (for example, 50 or 100
completed HHCAHPS surveys). At the same time, we also wanted to be able
to provide star ratings for as many HHAs as possible. This goal was
best served by using a lower minimum of completed HHCAHPS surveys (for
example, 20 completed HHCAHPS surveys). We chose to balance these
opposing and necessary goals by using 40 completed HHCAHPS surveys for
the Patient Survey Star Ratings. Because we believe that aligning the
Patient Survey Star Ratings system and the HHVBP Model provides
uniformity, consistency, and standard transformability for different
healthcare platforms, we proposed using a minimum of 40 instead of 20
completed HHCAHPS surveys under the HHVBP Model (82 FR 35333).
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\14\ Patient Survey Star Ratings https://www.medicare.gov/HomeHealthCompare/Data/Patient-Survey-Star-Ratings.html.
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In the CY 2018 HH PPS proposed rule (82 FR 35333), we noted that we
received a comment in response to the CY 2016 HH PPS proposed rule in
support of using a higher minimum threshold for HHCAHPS completed
surveys for the Patient Survey Star Ratings if the data are going to be
used in HHVBP or any other quality assessment program. We also noted
that we received public comment in response to the CY 2017 HH PPS
proposed rule in support of using a higher minimum threshold for
HHCAHPS completed surveys in the HHVBP Model, including a
recommendation to use a minimum of 100 HHCAHPS rather than a sample
size of 20 surveys (82 FR 35333). We stated in the CY 2018 HH PPS
proposed rule (82 FR 35333) that we believe that proposing a minimum of
40 completed HHCAHPS surveys for the Model would be more appropriate
than the higher minimums previously recommended by some commenters
because it represents a balance between providing meaningful data and
having sufficient numbers of HHAs with performance scores for at least
5 measures in the cohorts. Moreover, using a minimum of 40 completed
HHCAHPS surveys aligns with the Patient Survey Star Ratings on Home
Health Compare (82 FR 35333).
To understand the possible impact of our proposal to use a minimum
of 40 HHCAHPS completed surveys, we noted in the CY 2018 HH PPS
proposed rule (82 FR 35333) that HHAs may refer to the Interim
Performance Reports (IPRs) issued in October 2016, January 2017 and
April 2017, which analyzed 40 or more completed HHCAHPS surveys to
determine each HHA's HHCAHPS quality measure scores. As a point of
comparison to the minimum of 40 HHCAHPS completed surveys, these IPRs
were reissued using a minimum of 20 or more completed HHCAHPS surveys
and included quality measure scores, for these same time periods,
calculated with HHAs that qualify for the LEF by having sufficient data
for at least five measures. HHAs had the opportunity to submit a
request for recalculation of the revised interim performance scores.
HHAs had an opportunity to evaluate these IPRs in light of the
proposal to change to a minimum of 40 HHCAHPS completed surveys, as
well as seek clarification on the difference in their reports. The
participating HHAs received concurrent IPRs in July 2017 and concurrent
Annual Total Performance Score and Payment Adjustment Reports, which we
made available in August 2017. The concurrent reports showed one report
with HHCAHPS quality measure scores calculated based on a minimum of 40
completed surveys and one report with HHCAHPS quality measure scores
calculated based on a minimum of 20
[[Page 51702]]
completed surveys. Because the CY 2018 HH PPS proposed rule would not
be finalized before the timeline for submission of recalculation and
reconsideration requests, we noted HHAs would have the opportunity to
submit recalculation requests for the interim performance scores based
on both a minimum of 40 and 20 completed surveys, and recalculation and
reconsideration requests, as applicable, for the annual total
performance scores included in these reports for these thresholds in
accordance with the appeals process set forth at Sec. 484.335, which
was finalized in the CY 2017 HH PPS final rule (82 FR 35333).
As discussed in the CY 2018 HH PPS proposed rule (82 FR 35333
through 35334), we analyzed the effects on participating HHAs of using
the proposed 40 or more completed HHCAHPS surveys as compared to using
20 or more completed HHCAHPS surveys by examining OASIS measures
submitted from January 1, 2015 through December 31, 2016, claims
measures submitted from September 1, 2015 through September 30, 2016,
and 12 months ending June 30, 2016 for HHCAHPS-based measures. We found
that achievement thresholds, which are calculated as the median of all
HHAs' performance on the specified quality measures during the 2015
baseline year for each state, would not change by more than 1.1 percent, with the largest changes occurring in the statewide
achievement thresholds for the HHCAHPS Willingness to Recommend the
Agency measure in Arizona (+1.1 percent) and Nebraska (-1.1 percent).
Benchmarks (the mean of the top decile of Medicare-certified HHA
performance on the specified quality measures during the 2015 baseline
year, calculated for each state) had greater potential for change,
ranging down to -3.2 percent. For instance, we found that when
calculated using a minimum of 40 surveys rather than a minimum of 20
surveys, there was a -2.0 percent change in the benchmark for the
HHCAHPS Willingness to Recommend the Agency measure for Arizona and a -
1.7 percent change in the benchmark for Nebraska. We also found that
when calculated using a minimum of 40 surveys rather than a minimum of
20 surveys, there was a -1.7 percent change in the benchmark for the
HHCAHPS Communications between Providers and Patients measure for
Arizona, a -1.7 percent change in the benchmark for Florida, and a -3.2
percent change in the benchmark for Nebraska. Overall, the proposed
change in the HHCAHPS minimum of 40 completed surveys was estimated to
result in a limited percent change in the average statewide TPS for
larger-volume HHAs, ranging from -0.4 through +2.2 percent. We provided
estimates of the expected payment adjustment distribution based on the
proposed minimum of 40 completed HHCAHPS surveys in the impact analysis
of the CY 2018 HH PPS proposed rule (82 FR 35387).''
We invited public comment on our proposal to use 40 or more
completed HHCAHPS surveys as the minimum to generate a quality measure
score on the HHCAHPS measures, as is currently used in Home Health
Compare and the Patient Survey Star Ratings. Therefore, we proposed to
revise the definition of ``applicable measure'' at Sec. 484.305 from a
measure for which the competing HHA has provided 20 home health
episodes of care per year to a measure for which a competing HHA has
provided a minimum of 20 home health episodes of care per year for the
OASIS-based measures, 20 home health episodes of care per year for the
claims-based measures, or 40 completed surveys for the HHCAHPS
measures. We proposed that if finalized, this policy would apply to the
calculation of the benchmark and achievement thresholds and the
calculation of performance scores for all Model years, beginning with
PY 1.
The following is a summary of the public comments received on this
proposal and our responses:
Comment: Most commenters supported CMS' proposal to adjust the
minimum number of completed Home Health Care Consumer Assessment of
Healthcare Providers and System (HHCAHPS) Surveys. Several of these
commenters expressed that it will result in more reliable and valid
data results, as well as better align with the Patient Survey Star
Ratings policy. A few commenters expressed concern about the proposed
change and that using a minimum of 40 completed HHCAHPS surveys will
greatly reduce the number of agencies with data sufficient for Model
participation. A commenter specifically requested that CMS provide a
clear and separate announcement regarding the change in survey minimum,
how to interpret changes in total performance scores, and how to engage
in the appeals process. Finally, a few commenters were concerned that
smaller volume agencies will be negatively impacted, or forced to
close, given the shift from 20 to 40 completed HHCAHPS surveys.
Response: We appreciate commenters' support for our proposal to use
a minimum of 40 completed HHCAHPS surveys, rather than a minimum of 20
completed HHCAHPS surveys. We continue to believe that a minimum of 40
completed HHCAHPS surveys, rather than a minimum of 20 completed
HHCAHPS surveys, better aligns the Model with HHCAHPS policy for the
Patient Survey Star Ratings on Home Health Compare. As discussed in the
proposed rule, we believe that aligning the Patient Survey Star Ratings
and the HHVBP Model will provide uniformity, consistency, and standard
transformability for different healthcare platforms. While we recognize
that this change could result in fewer agencies receiving a measure
score on the HHCAHPS measures, we believe, as indicated in the proposed
rule, that using a minimum of 40 completed HHCAHPS surveys represents
an appropriate balance between providing meaningful data and having
sufficient numbers of HHAs with performance scores on five other
measures (for example OASIS based and claims based) to be included in
the LEF. As we discuss later in this section, however, our updated
analysis using full CY 2016 data found that no HHA fell below the
minimum of having five measures to generate a TPS as a result of using
a minimum of 40 rather than 20 completed HHCAHPs surveys.
For purposes of this final rule, we analyzed the effects on
participating HHAs of using the proposed 40 or more completed HHCAHPS
surveys as compared to using 20 or more completed HHCAHPS surveys by
examining OASIS, claims and HHCAHPS measures from January 1, 2016 to
December 31, 2016. We found that achievement thresholds will not change
by more than 1.1 percent, with the largest changes
occurring in the statewide achievement thresholds for the HHCAHPS
Willingness to Recommend the Agency measure in Arizona (+1.1 percent)
and Nebraska (-1.1 percent). Benchmarks continued to have greater
potential for change, ranging down to -3.1 percent. For instance, we
found that when calculated using a minimum of 40 surveys rather than a
minimum of 20 surveys, there was a -2.0 percent change in the benchmark
for the HHCAHPS Willingness to Recommend the Agency measure for Arizona
and a -1.7 percent change in the benchmark for Nebraska. We also found
that when calculated using a minimum of 40 surveys rather than a
minimum of 20 surveys, there was a -1.6 percent change in the benchmark
for the HHCAHPS Communications between Providers and
[[Page 51703]]
Patients measure for Arizona, a -1.7 percent change in the benchmark
for Florida, and a -3.1 percent change in the benchmark for Nebraska.
Overall, based on this updated analysis using full CY 2016 data,
the proposed change in the HHCAHPS minimum of 40 completed surveys was
estimated to result in a limited percent change in the average
statewide TPS for larger-volume HHAs, ranging from -0.3 percent through
+1.8 percent and the majority of the states were close to zero.
Additionally, the updated analysis using full CY 2016 data found that
there were no Medicare-certified HHAs in the selected states that fell
below the minimum of having five measures to generate a TPS for CY 2018
as a result of using a minimum of 40 rather than 20 completed HHCAHPs
surveys.
To provide HHAs with information on the effects of using a minimum
of 40 completed HHCAHPS surveys, rather than a minimum of 20 completed
HHCAHPS surveys, we reissued the October 2016, January 2017 and April
2017 IPRs, which analyzed 40 or more completed HHCAHPS surveys, so that
they could be recalculated with HHAs that have 20 or more completed
HHCAHPS surveys. Moreover, CMS provided HHAs with concurrent IPRs in
July 2017 and concurrent Annual Total Performance Score and Payment
Adjustment Reports in August 2017 to show one report with HHCAHPS
quality measure scores calculated based on a minimum of 40 completed
surveys and one report with HHCAHPS quality measure scores calculated
based on a minimum of 20 completed surveys. HHAs also had the
opportunity to submit recalculation requests for the interim
performance scores and recalculation and reconsideration requests, as
applicable, for the annual total performance scores, in accordance with
the process set forth at Sec. 484.335. Additionally, we provided a
number of webinars and other information on the interpretation of the
quality measure scores and the Total Performance Scores and on the
appeals process. More specifically, we provided all HHAs with a
questions and answers document on the use of HHCAHPS measures in HHVBP
Model performance reports when the reissued and concurrent IPRs were
made available. These reports and communications provided points of
comparison, clarification and information on the potential impact of
using a minimum of 40 completed HHCAHPS surveys, rather than a minimum
of 20 completed HHCAHPS surveys, to generate a quality measure score on
the HHCAHPS measures. CMS notes that no recalculation requests on the
reissued and concurrent IPRs were received and no recalculation or
reconsideration requests on the concurrent Annual Reports were received
that related to our proposal to change to the minimum of 40 completed
HHCAHPS surveys.
The change from a minimum of 20 completed HHCAHPS surveys to a
minimum of 40 completed HHCAHPS surveys was not intended to negatively
impact smaller agencies. We do not believe smaller HHAs will be
disadvantaged by this change to a minimum of 40, because given their
exemption from HHCAHPS reporting requirements, it is unlikely they
would be measured on HHCAHPS under the Model and they can still compete
on other measures.
We will continue to monitor the impacts of using a minimum of 40
completed HHCAHPS surveys, rather than a minimum of 20 completed
HHCAHPS surveys, for purposes of receiving a performance score for any
of the HHCAHPS measures.
Comment: A commenter suggested that because one negative survey
might affect a score based on a minimum of 20 completed HHCAHPS
surveys, removing the lowest and highest HHCAHPS for HHAs may be an
effective method to align with the average customer response.
Response: We believe this comment is outside of the scope of the
proposed methodology change in the CY 2018 HH PPS proposed rule to use
a minimum of 40 completed HHCAHPS surveys rather than a minimum of 20
completed HHCAHPS surveys. However, we note that we believe each
HHCAHPS survey may be an important avenue for public quality reporting
and continued improvement within the HHA environment.
Final Decision: For the reasons stated previously and in
consideration of the comments received, we are finalizing our proposal
to amend the definition of ``applicable measure'' to mean a measure for
which a competing HHA has provided a minimum of 40 completed surveys
for HHCAHPS measures, for purposes of receiving a performance score for
any of the HHCAHPS measures, beginning with PY1. In addition, we are
finalizing a few minor technical edits to the regulation at Sec.
484.305 to replace the colon and spell out ``twenty'' and ``forty''
(rather than ``20'' and ``40'').
2. Removal of One OASIS-Based Measure Beginning With Performance Year 3
In the CY 2016 HH PPS final rule, we finalized a set of quality
measures in Figure 4a: Final PY1 Measures and Figure 4b: Final PY1 new
measures (80 FR 68671 through 68673) for the HHVBP Model to be used in
PY 1, referred to as the starter set.
The measures were selected for the Model using the following
guiding principles: (1) Use a broad measure set that captures the
complexity of the services HHAs provide; (2) Incorporate the
flexibility for future inclusion of the Improving Medicare Post-Acute
Care Transformation Act of 2014 (IMPACT) measures that cut across post-
acute care settings; (3) Develop `second generation' (of the HHVBP
Model) measures of patient outcomes, health and functional status,
shared decision making, and patient activation; (4) Include a balance
of process, outcome and patient experience measures; (5) Advance the
ability to measure cost and value; (6) Add measures for appropriateness
or overuse; and (7) Promote infrastructure investments. This set of
quality measures encompasses the multiple National Quality Strategy
(NQS) domains \15\ (80 FR 68668). The NQS domains include six priority
areas identified in the CY 2016 HH PPS final rule (80 FR 68668) as the
CMS Framework for Quality Measurement Mapping. These areas are: (1)
Clinical quality of care; (2) care coordination; (3) population &
community health; (4) person- and caregiver-centered experience and
outcomes; (5) safety; and (6) efficiency and cost reduction. Figures 4a
and 4b of the CY 2016 HH PPS final rule (80 FR 68671 through 68673)
identified 15 outcome measures (five from the HHCAHPS, eight from
Outcome and Assessment Information Set (OASIS), and two from the
Chronic Care Warehouse (claims)), and nine process measures (six from
OASIS, and three new measures, which were not previously reported in
the home health setting).
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\15\ 2015 Annual Report to Congress, https://www.ahrq.gov/workingforquality/reports/annual-reports/nqs2015annlrpt.htm.
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In the CY 2017 HH PPS final rule (81 FR 76743 through 76747), we
removed the following four measures from the measure set for PY 1 and
subsequent performance years: (1) Care Management: Types and Sources of
Assistance; (2) Prior Functioning ADL/IADL; (3) Influenza Vaccine Data
Collection Period: Does this episode of care include any dates on or
between October 1 and March 31?; and (4) Reason Pneumococcal Vaccine
Not Received, for the reasons discussed in that final rule.
For PY 3, we proposed to remove one OASIS-based measure, Drug
Education
[[Page 51704]]
on All Medications Provided to Patient/Caregiver during All Episodes of
Care, from the set of applicable measures (82 FR 35334). We stated in
the CY 2018 HH PPS proposed rule that, as part of our ongoing
monitoring efforts, we found that based on the standard metrics of
measure performance, many providers have achieved full performance on
the Drug Education measure. For example, for the January 2017 IPRs
(which covered the 12-month period of October 1, 2015 through September
30, 2016), the average value for this measure across all participating
HHAs was 95.69 percent from October 2015 through September 2016. When
looking at September 2016, the mean value on this measure across all
participating HHAs had increased to 97.8 percent. In addition, we noted
that there are few HHAs with poor performance on the measure. Based on
the January 2017 IPRs, across all participating HHAs, the 10th
percentile was 89 percent and the 5th percentile was 81.8 percent, but
only 1.8 percent of HHAs had a value below 70 percent on the measure.
We stated in the CY 2018 HH PPS proposed rule (82 FR 35334) that we
believe that removing this measure would be consistent with our policy,
as noted in the CY 2017 HH PPS final rule (81 FR 76746), that when a
measure has achieved full performance, we may propose the removal of
the measure in future rulemaking. In addition, our contractor's
Technical Expert Panel (TEP), which consists of 11 panelists with
expertise in home health care and quality measures, expressed concern
that the Drug Education measure does not capture whether the education
provided by the HHA was meaningful.
We presented the revised set of applicable measures, reflecting our
proposal to remove the OASIS-based measure, Drug Education on All
Medications Provided to Patient/Caregiver during All Episodes of Care,
in Table 43 of the CY 2018 HH PPS proposed rule. We stated that this
measure set would be applicable to PY3 and each subsequent performance
year until such time that another set of applicable measures, or
changes to this measure set, are proposed and finalized in future
rulemaking (82 FR 35334 through 35336).
We invited public comment on the proposal to remove one OASIS-based
measure, Drug Education on All Medications Provided to Patient/
Caregiver during All Episodes of Care, from the set of applicable
measures for PY3 and subsequent performance years and Table 43 of the
CY 2018 HH PPS proposed rule. The following is a summary of the public
comments received on this proposal and our responses:
Comment: Several commenters expressed support for removing the
OASIS-based quality measure, Drug Education on All Medications Provided
to Patient/Caregiver during All Episodes of Care, from the set of
applicable measures as it has ``topped out.''
Response: We appreciate the support regarding the proposed removal
of the ``Drug Education'' measure from the HHVBP Model's set of
applicable measures because it has ``topped out''. We are finalizing
the removal of the ``Drug Education'' measure as most providers have
achieved full performance on the measure.
Comment: Several commenters provided feedback regarding the measure
set more generally and some were outside of the scope of the proposed
change. A commenter recommended that CMS consider assigning 50 percent
of the ``Star Rating'' and HHVBP performance to claims-based measures
and Patient Satisfaction, as the commenter believed that these measures
are difficult or impossible to manipulate, and then assign the other 50
percent to OASIS-based self-reported measures. A commenter expressed
concern that the measure set for the HHVBP Model mainly requires
improvement in patient functioning and that this conflicts directly
with the Jimmo v. Sebelius settlement.\16\ Another commenter
recommended replacing the Pneumococcal Polysaccharide Vaccine Ever
Received (NQF#0525) because the measure no longer reflects current
recommendations of the Advisory Committee for Immunization Practice
(ACIP).
---------------------------------------------------------------------------
\16\ Jimmo v. Sebelius Settlement Agreement Fact Sheet: https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/SNFPPS/Downloads/Jimmo-FactSheet.pdf.
---------------------------------------------------------------------------
Response: We appreciate the comments on the measures methodology
and, as discussed in the CY 2016 HH PPS final rule (80 FR 68669) and CY
2017 HH PPS final rule (81 FR 76747), acknowledge that skilled care may
be necessary to improve a patient's current condition, to maintain the
patient's current condition, or to prevent or slow further
deterioration of the patient's condition, as was clarified through the
provisions revised as part of Jimmo v. Sebelius settlement. As stated
in those rules, this settlement agreement pertains only to the
clarification of CMS's manual guidance on coverage standards, not
payment measures like those at issue here, and expressly does not
pertain to or prevent the implementation of new regulations, including
new regulations pertaining to the HHVBP Model. We refer readers to the
CY 2016 HH PPS final rule (80 FR 68669 through 68670) for additional
discussion of our analyses of measure selection, including our analyses
of existing measures relating to improvement and stabilization. As
discussed in that rule, the HHVBP Model is designed such that any
measures determined to be good indicators of quality will be considered
for use in the HHVBP Model in future years and may be added through the
rulemaking process. As discussed in prior years, we will continue to
seek and consider input we have received on the measure set for the
HHVBP Model.
Final Decision: We are finalizing our proposal to remove the OASIS-
based measure, Drug Education on All Medications Provided to Patient/
Caregiver during All Episodes of Care, from the set of applicable
measures for PY3 and subsequent years, as reflected in Table 15. Table
15 identifies the applicable measures set for PY3 and each subsequent
performance year until such time that another set of applicable
measures, or changes to this measure set, are proposed and finalized in
future rulemaking.
Table 15--Measure Set for the HHVBP Model* Beginning PY 3
--------------------------------------------------------------------------------------------------------------------------------------------------------
NQS domains Measure title Measure type Identifier Data source Numerator Denominator
--------------------------------------------------------------------------------------------------------------------------------------------------------
Clinical Quality of Care...... Improvement in Outcome.......... NQF0167.......... OASIS (M1860).... Number of home health Number of home health
Ambulation- episodes of care episodes of care
Locomotion. where the value ending with a
recorded on the discharge during the
discharge assessment reporting period,
indicates less other than those
impairment in covered by generic
ambulation/ or measure-specific
locomotion at exclusions.
discharge than at
the start (or
resumption) of care.
[[Page 51705]]
Clinical Quality of Care...... Improvement in Outcome.......... NQF0175.......... OASIS (M1850).... Number of home health Number of home health
Bed Transferring. episodes of care episodes of care
where the value ending with a
recorded on the discharge during the
discharge assessment reporting period,
indicates less other than those
impairment in bed covered by generic
transferring at or measure-specific
discharge than at exclusions.
the start (or
resumption) of care.
Clinical Quality of Care...... Improvement in Outcome.......... NQF0174.......... OASIS (M1830).... Number of home health Number of home health
Bathing. episodes of care episodes of care
where the value ending with a
recorded on the discharge during the
discharge assessment reporting period,
indicates less other than those
impairment in covered by generic
bathing at discharge or measure-specific
than at the start exclusions.
(or resumption) of
care.
Clinical Quality of Care...... Improvement in Outcome.......... NA............... OASIS (M1400).... Number of home health Number of home health
Dyspnea. episodes of care episodes of care
where the discharge ending with a
assessment indicates discharge during the
less dyspnea at reporting period,
discharge than at other than those
start (or covered by generic
resumption) of care. or measure-specific
exclusions.
Communication & Care Discharged to Outcome.......... NA............... OASIS (M2420).... Number of home health Number of home health
Coordination. Community. episodes where the episodes of care
assessment completed ending with
at the discharge discharge or
indicates the transfer to
patient remained in inpatient facility
the community after during the reporting
discharge. period, other than
those covered by
generic or measure-
specific exclusions.
Efficiency & Cost Reduction... Acute Care Outcome.......... NQF0171.......... CCW (Claims)..... Number of home health Number of home health
Hospitalization: stays for patients stays that begin
Unplanned who have a Medicare during the 12-month
Hospitalization claim for an observation period.
during first 60 unplanned admission A home health stay
days of Home to an acute care is a sequence of
Health. hospital in the 60 home health payment
days following the episodes separated
start of the home from other home
health stay. health payment
episodes by at least
60 days.
Efficiency & Cost Reduction... Emergency Outcome.......... NQF0173.......... CCW (Claims)..... Number of home health Number of home health
Department Use stays for patients stays that begin
without who have a Medicare during the 12-month
Hospitalization. claim for outpatient observation period.
emergency department A home health stay
use and no claims is a sequence of
for acute care home health payment
hospitalization in episodes separated
the 60 days from other home
following the start health payment
of the home health episodes by at least
stay. 60 days.
Patient Safety................ Improvement in Outcome.......... NQF0177.......... OASIS (M1242).... Number of home health Number of home health
Pain Interfering episodes of care episodes of care
with Activity. where the value ending with a
recorded on the discharge during the
discharge assessment reporting period,
indicates less other than those
frequent pain at covered by generic
discharge than at or measure-specific
the start (or exclusions.
resumption) of care.
Patient Safety................ Improvement in Outcome.......... NQF0176.......... OASIS (M2020).... Number of home health Number of home health
Management of episodes of care episodes of care
Oral Medications. where the value ending with a
recorded on the discharge during the
discharge assessment reporting period,
indicates less other than those
impairment in taking covered by generic
oral medications or measure-specific
correctly at exclusions.
discharge than at
start (or
resumption) of care.
Population/Community Health... Influenza Process.......... NQF0522.......... OASIS (M1046).... Number of home health Number of home health
Immunization episodes during episodes of care
Received for which patients (a) ending with
Current Flu received vaccination discharge, or
Season. from the HHA or (b) transfer to
had received inpatient facility
vaccination from HHA during the reporting
during earlier period, other than
episode of care, or those covered by
(c) was determined generic or measure-
to have received specific exclusions.
vaccination from
another provider.
Population/Community Health... Pneumococcal Process.......... NQF0525.......... OASIS (M1051).... Number of home health Number of home health
Polysaccharide episodes during episodes of care
Vaccine Ever which patients were ending with
Received. determined to have discharge or
ever received transfer to
Pneumococcal inpatient facility
Polysaccharide during the reporting
Vaccine (PPV). period, other than
those covered by
generic or measure-
specific exclusions.
Patient & Caregiver-Centered Care of Patients. Outcome.......... ................. CAHPS............ NA................... NA.
Experience.
Patient & Caregiver-Centered Communications Outcome.......... ................. CAHPS............ NA................... NA.
Experience. between
Providers and
Patients.
Patient & Caregiver-Centered Specific Care Outcome.......... ................. CAHPS............ NA................... NA.
Experience. Issues.
Patient & Caregiver-Centered Overall rating of Outcome.......... ................. CAHPS............ NA................... NA.
Experience. home health care.
[[Page 51706]]
Patient & Caregiver-Centered Willingness to Outcome.......... ................. CAHPS............ NA................... NA.
Experience. recommend the
agency.
Population/Community Health... Influenza Process.......... NQF0431 (Used in Reported by HHAs Healthcare personnel Number of healthcare
Vaccination other care through Web in the denominator personnel who are
Coverage for settings, not Portal. population who working in the
Home Health Care Home Health). during the time from healthcare facility
Personnel. October 1 (or when for at least 1
the vaccine became working day between
available) through October 1 and March
March 31 of the 31 of the following
following year: a) year, regardless of
received an clinical
influenza responsibility or
vaccination patient contact.
administered at the
healthcare facility,
or reported in
writing or provided
documentation that
influenza
vaccination was
received elsewhere:
or b) were
determined to have a
medical
contraindication/
condition of severe
allergic reaction to
eggs or to other
components of the
vaccine or history
of Guillain-Barre
Syndrome within 6
weeks after a
previous influenza
vaccination; or c)
declined influenza
vaccination; or d)
persons with unknown
vaccination status
or who do not
otherwise meet any
of the definitions
of the above-
mentioned numerator
categories.
Population/Community Health... Herpes zoster Process.......... NA............... Reported by HHAs Total number of Total number of
(Shingles) through Web Medicare Medicare
vaccination: Has Portal. beneficiaries aged beneficiaries aged
the patient ever 60 years and over 60 years and over
received the who report having receiving services
shingles ever received zoster from the HHA.
vaccination? vaccine (shingles
vaccine).
Communication & Care Advance Care Plan Process.......... NQF0326.......... Reported by HHAs Patients who have an All patients aged 65
Coordination. through Web advance care plan or years and older.
Portal. surrogate decision
maker documented in
the medical record
or documentation in
the medical record
that an advanced
care plan was
discussed but the
patient did not wish
or was not able to
name a surrogate
decision maker or
provide an advance
care plan.
--------------------------------------------------------------------------------------------------------------------------------------------------------
* Notes: For more detailed information on the measures utilizing OASIS refer to the OASIS-C1/ICD-9, Changed Items & Data Collection Resources dated
September 3, 2014 available at www.oasisanswers.com/LiteratureRetrieve.aspx?ID=215074. For NQF endorsed measures see The NQF Quality Positioning
System available at https://www.qualityforum.org/QPS. For non-NQF measures using OASIS see links for data tables related to OASIS measures at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html. For information on HHCAHPS
measures see https://homehealthcahps.org/SurveyandProtocols/SurveyMaterials.aspx.
C. Quality Measures for Future Consideration
The CY 2016 HH PPS final rule discusses the HHVBP Model design, the
guiding principles to select measures, and the six priority areas of
the National Quality Strategy (NQS) we considered for the Model (80 FR
68656 through 68678). Under the HHVBP Model, any measures we determine
to be good indicators of quality will be considered for use in the
HHVBP Model in future years, and may be added or removed through the
rulemaking process. To further our commitment to objectively assess
HHVBP quality measures, we are utilizing an implementation contractor
that invited a group of measure experts to provide advice on the
adjustment of the current measure set for consideration. The contractor
convened a technical expert panel (TEP) consisting of 11 panelists with
expertise in home health care and quality measures that met on
September 7, 2016, in Baltimore, Maryland and via conference call on
December 2, 2016. The TEP discussed developing a composite total change
in ADL/IADL measure; a composite functional decline measure; a measure
to capture when an HHA correctly identifies the patient's need for
mental and behavioral health supervision; and a measure to identify if
a caregiver is able to provide the patient's mental or behavioral
health supervision, to align with Sec. 409.45(b)(3)(iii) and the
Medicare Benefit Policy Manual (Pub. 100-02), Chapter 7, Section 20.2.
We discussed each of these potential measures in further detail in the
CY 2018 HH PPS proposed rule (82 FR 35336 through 35340), and also
discuss in this section of this final rule. While any new measures
would be proposed for use in future rulemaking, we solicited comment on
these potential measures now to inform measure development and
selection.
As noted in the CY 2017 HH PPS final rule (81 FR 76747), we
received several comments expressing concern that the measures under
the Model do not reflect the patient population served under the
Medicare Home Health benefit as the outcome measures focus on a
patient's clinical improvement and do not address patients with chronic
illnesses; deteriorating neurological, pulmonary, cardiac, and other
conditions; and some with terminal illness. The commenters opined that
the value of including stabilization measures in the HHVBP Model is
readily apparent as it aligns the Model with the Medicare Home Health
benefit. Commenters also expressed concerns that improvement is not
always the goal for each patient and
[[Page 51707]]
that stabilization is a reasonable clinical goal for some patients.
Commenters suggested the addition of stabilization or maintenance
measures be considered for the HHVBP Model. Many commenters objected to
the use of improvement measures in the HHVBP Model. We did not receive
any specific measures for future consideration as part of those
comments. In the CY 2018 HH PPS proposed rule (82 FR 35336 through
35340), we identified measures that we are considering for possible
inclusion under the Model in future rulemaking and sought input from
the public on the measures described, as well as any input about the
development or construction of the measures and their features or
methodologies. We are also including the description of these possible
measures in this final rule in the subsections that follow.
1. Total Change in ADL/IADL Performance by HHA Patients
The measure set finalized in the CY 2016 HH PPS final rule included
Change in Daily Activity Function as Measured by the Activity Measure
for Post-Acute Care (AM-PAC) (NQF #0430). However, the measure was
removed in the CY 2017 HH PPS final rule and never used in the HHVBP
Model because the measure required use of a proprietary data collection
instrument in the home health environment. We stated in the CY 2018 HH
PPS proposed rule that we were considering replacing Change in Daily
Activity Function as Measured by AM-PAC (NQF #0430) with a composite
total ADL/IADL change performance measure. During the September 2016
TEP meeting, an alternative to the Change in Daily Activity Function
measure was presented. The TEP requested that a composite Total ADL/
IADL Change measure be investigated empirically. This measure was
discussed as part of the follow-up conference call, and the TEP
supported continued development of the measure in the HHVBP Model as a
way of including a measure that captures all three potential outcomes
for home health patients: stabilization; decline; and improvement. They
provided input on the technical specifications of the potential
composite measure, including the feasibility of implementing the
measure and the overall measure reliability and validity. We noted in
the CY 2018 HH PPS proposed rule that we reviewed this suggested
alternative and believe this measure would provide actionable and
transparent information that would support HHA efforts to improve care
and prevent functional decline for all patients across a broad range of
patient functional outcomes. The measure would also improve
accountability during an episode of care when the patient is directly
under the HHA's care.
We noted in the CY 2018 HH PPS proposed rule that the name of this
potential composite measure could be Total Change in ADL/IADL
Performance by HHA Patients. The measure would report the average,
normalized, total improved functioning across the 11 ADL/IADL items on
the current OASIS-C2 instrument. The measure is calculated by comparing
scores from the start-of-care/resumption of care to scores at
discharge. For each item the patient's discharge assessed performance
score is subtracted from the patient's start of care/resumption of care
assessed performance score, and then divided by the maximum improvement
value based on the number of response options for that item. These
values are summed into a total normalized change score that can range
from -11 (that is, for an episode where there is maximum decline on all
11 items used in the measure) to +11 (that is, for an episode where
there is the maximum improvement on all 11 items). An HHA's score on
the measure is based on its average across all eligible episodes.
Patients who are independent on all 11 ADL/IADL items at Start of Care
(SOC)/Resumption of Care (ROC) would also be included in the measure.
The HHA's observed score on the measure is the average of the
normalized total scores for all eligible episodes for its patients
during the reporting period.
The following 11 ADLs/IADL-related items from OASIS-C2 items were
included in developing a composite measure:
ADL OASIS-C2 items related to Self-Care:
M1800 (Grooming).
M1810 (Upper body dressing).
M1820 (Lower body dressing).
M1845 (Toileting hygiene).
M1870 (Eating).
ADL OASIS-C2 items related to Mobility:
M1840 (Toilet transferring).
M1840 (Bed transferring).
M1860 (Ambulation).
Other IADLs OASIS items:
M1880 (Light meal preparation).
M1890 (Telephone use).
M2020 (Oral medication management).
Based on these identified measures, we would risk-adjust using
OASIS-C2 items to account for case-mix variation and other factors that
affect functional decline but are outside the influence of the HHA. The
risk-adjustment model uses an ordinary least squares (OLS)
17 18 regression framework because the outcome measure
(normalized change in ADL/IADL performance) is a continuous variable.
---------------------------------------------------------------------------
\17\ Fox, John (1997). Applied Regression Analysis, Linear
Models, and Related\Methods/Edition 1, 1997, SAGE.
\18\ Greene, William H. (2017). Econometric analysis (8th ed.).
New Jersey: Pearson. ISBN 978-0134461366.
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The prediction model for this outcome measure was derived using the
predicted values from the 11 individual outcomes that are currently
used to risk adjust these 11 individual quality measures. Of the 11
values tested, the 8 identified in the proposed rule were found to be
statistically related to the Total Change in ADL/IADL Performance by
HHA Patients measure at p < 0.0001 level and would be used in the
prediction model that we are considering proposing to use to risk
adjust the HHA's observed value for this potential future measure. The
prediction model for this outcome measure uses predicted values from
the following individual outcomes (NOTE: The primary source OASIS item
is listed in parenthesis after the name of the quality measure):
Improvement in Upper Body Dressing (M1810).
Improvement in Management of Oral Medications (M2020).
Improvement in Bed Transferring (M1850).
Improvement in Ambulation/Locomotion (M1860).
Improvement in Grooming (M1800).
Improvement in Toileting Hygiene (M1845).
Discharged to the Community (M2420).
Improvement in Toileting Transfer (M1840).
Two predictive models, one based on predicted values from CY 2014
and one from CY 2015, were computed. The correlations at the episode
level between observed and predicted values for the target outcome
measure Total Change in ADL/IADL Performance by HHA Patients are shown
in Table 16.
[[Page 51708]]
Table 16--Correlations at the Episode Level Between Observed and Predicted Values for the Target Outcome Measure
Total Change in ADL/IADL Performance by HHA Patients
----------------------------------------------------------------------------------------------------------------
r2 (Coeff.
Data group Correlation Significance Determination)
(p < ) %
----------------------------------------------------------------------------------------------------------------
CY2014, National................................................ 0.5022 0.0001 25.22
CY2014, HHVBP states............................................ 0.5094 0.0001 25.95
CY2015, National................................................ 0.5011 0.0001 25.11
CY2015, HHVBP states............................................ 0.5076 0.0001 25.76
----------------------------------------------------------------------------------------------------------------
The results in Table 16 suggest that either model would account for
25 percent or more of the variability in the outcome measure. These
models could be considered very strong predictive models for the target
outcome measure. Although the analysis supports developing a composite
measure, the analysis assumes that the OASIS-C2 items identified to be
used in the composite measure do not change. However, we recognize that
OASIS-C2 items could be removed or added in any given year. We expect
to conduct an additional analysis, in advance of any future proposal,
to assess whether changes to OASIS-C2 items that are removed or added
could significantly impact a HHA's ability to address several measures
to improve its overall score in the composite measure. We solicited
public comments on whether or not to include a composite total ADL/IADL
change performance measure in the set of applicable measures, the name
of any such measure, the risk adjustment method, and whether we should
conduct an analysis of the impact of removal/addition of OASIS-C2
items.
2. Composite Functional Decline Measure
The second measure we are considering for possible inclusion under
the Model in future rulemaking is a Composite Functional Decline
Measure that could be the percentage of episodes where there was
decline on one or more of the eight ADL items used in the measure. As
noted in the CY 2018 HH PPS proposed rule and this final rule, we
received comments on the CY 2017 HH PPS proposed rule suggesting that
we consider the addition of stabilization or maintenance measures. We
stated in the CY 2018 HH PPS proposed rule that to address this
suggestion, we are considering a composite functional decline measure
because the existing functional stabilization measures, taken
individually, are topped out, with HHA level means of 95 percent or
higher. This type of composite functional decline measure is similar to
the composite ADL decline measure that is used in the Skilled Nursing
Facility (SNF) Quality Reporting program (QRP).\19\ The SNF QRP measure
is constructed from four ADL items: Bed mobility; transfer; eating; and
toileting.
---------------------------------------------------------------------------
\19\ ``Long-stay Nursing Home Care: Percent of Residents Whose
Need for help with Activities of Daily Living has Increased.''
https://www.qualitymeasures.ahrq.gov/summaries/summary/50060.
---------------------------------------------------------------------------
An HHVBP composite functional decline measure could provide
actionable and transparent information that could support HHA efforts
to improve care and prevent functional decline for all patients,
including those for whom improvement in functional status is not a
realistic care goal. We noted in the CY 2018 HH PPS proposed rule that
this concept was discussed during the TEP meeting on September 7, 2016,
with a follow-up conference call held on December 2, 2016. The TEP
supported the inclusion of measures of stabilization and decline in the
HHVBP Model, as well as further development of the composite functional
decline measure. They provided input on the technical specifications of
the potential composite measure, including the feasibility of
implementing the measure and the overall measure reliability and
validity.
When calculating the composite functional decline measure, we noted
that we could use the following 8 existing OASIS-C2 items:
Ambulation/Locomotion (M1860).
Bed Transferring (M1840).
Toilet Transferring (M1840).
Bathing (M1830).
Toilet Hygiene (M1845).
Lower Body Dressing (M1820).
Upper Body Dressing (M1810).
Grooming (M1800).
We noted that the measure could be defined as 1 if there is decline
reported in one or more of these items between the Start of Care and
the Discharge assessments and zero if no decline is reported on any of
these items. As with other OASIS-based measures, a performance score
for the measure would only be calculated for HHAs that have 20 or more
episodes of care during a performance year.
The measure could be risk-adjusted using OASIS-C2 items to account
for case-mix variation and other factors that affect functional decline
but are outside of the influence of the HHA. The risk-adjustment model
uses a logistic regression framework. The model includes a large number
of patient clinical conditions and other characteristics measured at
start of care. A logistic regression model is estimated to predict
whether the patient will have a length of stay of greater than 60 days.
The predicted probability of a length of stay of greater than 60 days
is used, along with other patient characteristics, to construct a
logistic regression model to predict the probability of decline in any
of eight ADLs. This model is used to estimate the predicted percent of
ADL decline at the HHA level. To calculate case-mix adjusted values,
the observed value of the measure is adjusted by the difference between
the HHA predicted percent and the national predicted percent. The risk-
adjustment model reduces the adjusted difference between HHAs that
serve a disproportionate number of longer-stay patients and those that
serve patients with more typical lengths of stay of one episode.
Across all participating HHAs in the HHVBP Model, for HHAs that had
less than 20 percent of episodes lasting more than 60 days, the average
on the functional decline measure was 8.08 percent. This increased to
11.08 percent for HHAs with 20 percent to 40 percent of episodes
lasting more than 60 days, 14.23 percent for HHAs with 40 percent to 60
percent of episodes lasting more than 60 days, and 20.59 percent for
HHAs with more than 60 percent of episodes lasting more than 60 days.
This finding suggests that, in addition to focusing on prevention of
functional decline, we should also attempt to better predict a
patient's functional trajectory and potentially stratify the population
to exclude those on a likely downward trajectory. However, in spite of
this finding, the inclusion of a measure that rewards providers for
avoiding functional decline has the advantage of diversifying the set
of measures for the HHVBP model. We solicited public
[[Page 51709]]
comments on whether or not to include a composite functional decline
measure in the set of applicable measures, the name of any such
measure, the risk adjustment method, and whether we should conduct an
analysis of the impact of removal/addition of OASIS-C2 items.
3. Behavioral Health Measures
Although we did not receive comments or suggestions through the
rulemaking process for the HHVBP Model regarding behavioral or mental
health measures, we noted in the CY 2018 HH PPS proposed rule that we
recognize that the Model does not include such measures. The OASIS-C2
collects several items related to behavioral and mental health (M1700
Cognitive Functioning; M1710 Confusion Frequency; M1720 Anxiety; M1730
Depression Screening; M1740 Cognitive, Behavioral, and Psychiatric
Symptoms; M1745 Frequency of Disruptive Behavior Symptoms; and M1750
Psychiatric Nursing Services). These items are used to compute both
Improvement and Process measures as well as Potentially Avoidable
Events. The inclusion of behavioral health measures is important for
care transformation and improvement activities as many persons served
by the Home Health program may have behavioral health needs.
The TEP made several suggestions during the December 2016
conference call as to whether the focus of a behavioral or mental
health measure could be identifying whether a patient needed mental or
behavioral health assistance compared to the supervision of the patient
or advocacy assistance. The TEP supported the supervision type measure
due to its opportunity for potential improvement. In further analyses,
we identified two underlying components to outcomes for providing
assistance. We developed a method, described in the following section,
to identify patients who have or do not have needs for mental or
behavioral health supervision. We noted that we are considering further
refining this method by identifying the involvement of the caregiver in
addressing the patient's mental or behavioral health supervision needs
as an important outcome measure, and we solicited comment on whether
this is an appropriate factor or feature that we should consider in
developing such a measure in future rulemaking.
a. HHA Correctly Identifies Patient's Need for Mental or Behavioral
Health Supervision
We stated in the CY 2018 HH PPS proposed rule that we are
considering adding a HHA Correctly Identifies Patient's Need for Mental
or Behavioral Health Supervision measure to the HHVBP Model in the
future to capture a patient's need for mental or behavioral health
supervision based on an identifier. This identifier is based on
information from existing Neuro/Emotional/Behavioral Status OASIS
items, along with other indicators of mental/behavioral health problems
to identify a patient in need of supervisory assistance. The outcome
measure assesses whether the HHA correctly identifies whether or not
the patient needs mental or behavioral health supervision based on the
OASIS SOC/ROC assessment item M2102f, Types and Sources of Assistance:
Supervision and Safety.
A composite Mental/Behavioral Health measure could be a dichotomous
measure that reports the percentage of episodes of care where the HHA
correctly identifies: (a) Patients who need mental or behavioral health
supervision; and (b) patients who do not need mental or behavioral
health supervision. The numerator could be a combination of two values:
(1) The number of episodes of care where the HHA correctly identifies
patients who need mental or behavioral health supervision; plus (2) the
number of episodes of care where the HHA correctly identifies patients
who do not need mental or behavioral health supervision. The
denominator is all episodes of care.
The composite measure requires that a patient's need for mental or
behavioral health supervision be identified. The following algorithm
was designed to identify if a patient was in need of mental or
behavioral health supervision. If the patient met any of the following
conditions, the patient was identified by the algorithm as in need of
mental or behavioral health supervision:
Was discharged from a psychiatric hospital prior to
entering home health care (M1000 = 6).
Is diagnosed as having chronic mental behavioral problems
(M1021 and M1023).
Is diagnosed with a mental illness (M1021 and M1023).
Is cognitively impaired (M1700 >= 2).
Is confused (M1710 >= 2).
Is identified as having a memory deficit (M1740 = 1).
Is identified as having impaired decision-making (M1740 =
2).
Is identified as being verbally disruptive (M1740 = 3).
Is identified as being physically aggressive (M1740 = 4).
Is identified as exhibiting disruptive, infantile, or
inappropriate behaviors (M1740 = 5).
Is identified as being delusional (M1740 = 6).
Has a frequency of disruptive symptoms (M1745 >= 2).
The measure also requires that the HHA identify if the patient is
in need of mental or behavioral health supervision. This requirement is
based on the SOC/ROC code for M2102f, Types and Sources of Assistance:
Supervision and Safety. If the HHA codes a value of zero, then the HHA
has identified this patient as not needing mental or behavioral health
supervision. If the HHA codes another value for M2102f, Types and
Sources of Assistance: Supervision and Safety, then the HHA has
identified this patient as needing mental or behavioral health
supervision. The outcome measure is defined as the agreement between
the algorithm's identification of a patient's need for mental or
behavioral health supervision and the HHA's coding of this need. That
is, if--
The algorithm identifies the patient as not in need of
mental or behavioral health supervision and the HHA identifies the
patient as not in need of mental or behavioral health supervision; or
The algorithm identifies the patient as in need of mental
or behavioral health supervision and the HHA identifies the patient as
in need of mental or behavioral health supervision; then
The outcome is coded as 1, successful.
As with other OASIS-based measures, a performance score for the
measure would only be calculated for HHAs that have 20 or more episodes
of care during a performance year.
The measure is risk-adjusted using OASIS-C2 items to account for
case-mix variation and other factors that affect functional decline but
are outside the influence of the HHA. The risk-adjustment model uses a
logistic regression framework. The model includes a large number of
patient clinical conditions and other characteristics measured at the
start of care. To calculate case-mix adjusted values, the observed
value of the measure is adjusted by the difference between the HHA
predicted percent and the national predicted percent.
[[Page 51710]]
The prediction model for this outcome measure uses 39 risk factors
\20\ with each risk factor statistically significant at p<0.0001. The
correlation for the model between observed and predicted values as
estimated by Somers' D \21\ is 0.427, that yields an estimated
coefficient of determination (r2) value based on the Tau-a \22\ of
0.201. This suggests that the variability in the model accounts for
(predicts) approximately 20 percent of the variability in the outcome
measure. The best statistic for evaluating the power of a prediction
model that is derived using logistic regression is the c-statistic.\23\
This statistic identifies the overall accuracy of prediction by
comparing observed and predicted value pairs to the proportion of the
time that both predict the outcome in the same direction with 0.500
being a coin-flip. The discussed prediction model has a c-statistic
equal to 0.713, which is considered to be good. Using data from CY
2015, the episode-level mean for the HHA Correctly Identifies Patient's
Need for Mental or Behavioral Health Supervision measure is 61.98
percent, nationally, and 62.98 percent for the HHVBP states.
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\20\ ``Home Health Quality Initiative: Quality Measures''
https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html.
\21\ Somers' D is a statistic that is based on the concept of
concordant vs. discordant pairs for two related values. In this
case, if both the observed and predicted values are higher than the
average or if both values are less than the average, then the pair
of numbers is considered concordant. However, if one value is higher
than average and the other is lower than average--or vice versa,
then the pair of values is considered discordant. The Somer's D is
(# of concordant pairs--# of discordant pairs)/total # of pairs. The
higher the ratio, the stronger the concordance between the two set
of values.
\22\ The Kendall Tau-a assumes that if there is a correlation
between two variables, then sorting the variables based on one of
the values will result in ordering the second variable. It uses the
same concept of concordant pairs in Somers' D but a different
formula: t = [(4P)/[(n) (n-1)]--1 where p = # of concordant pairs
and n = # of pairs. This correlation method reduces the effect of
outlier values as the values are essentially ranked.
\23\ The C-statistic (sometimes called the ``concordance''
statistic or C-index) is a measure of goodness of fit for binary
outcomes in a logistic regression model. In clinical studies, the C-
statistic gives the probability a randomly selected patient who
experienced an event (for example, a disease or condition) had a
higher risk score than a patient who had not experienced the event.
It is equal to the area under the Receiver Operating Characteristic
(ROC) curve and ranges from 0.5 to 1.
A value below 0.5 indicates a very poor model.
A value of 0.5 means that the model is no better than
predicting an outcome than random chance.
Values over 0.7 indicate a good model.
Values over 0.8 indicate a strong model.
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b. Caregiver Can/Does Provide for Patient's Mental or Behavioral Health
Supervision Need
We stated in the CY 2018 HH PPS proposed rule that we are
considering including under the Model in future rulemaking a Caregiver
Can/Does Provide for Patient's Mental or Behavioral Health Supervision
Need measure that would encourage HHAs to ensure that patients who need
mental or behavioral health supervision are receiving such care from
the patient's caregivers, and would be a realistic care goal.
When considering how to develop a measure to determine whether or
not the caregiver can/does provide the patient's mental or behavioral
health supervision, we would create an identifier of a patient's need
for mental or behavioral health supervision. This identifier is based
on the same algorithm described in the previous section from existing
Neuro/Emotional/Behavioral Status OASIS items along with other
indicators of mental/behavioral health problems to identify a patient
in need of supervisory assistance. The outcome measure is whether the
HHA correctly identifies this patient as having the need for mental or
behavioral health supervision based on the OASIS SOC/ROC assessment
item M2102f, Types and Sources of Assistance: Supervision and Safety.
The measure could be a dichotomous measure that reports the
percentage of episodes where patients with identified mental or
behavioral health supervision needs have their needs met or could have
their needs met by the patient's caregiver with additional training (if
needed) and support by the HHA. The numerator is the intersection of
the number of episodes of care where: (1) The patient needs mental or
behavioral health supervision; and (2) these patients have their needs
met or could have their needs met by the patient's caregiver with
additional training (if needed) and support by the HHA. By
intersection, we mean that, for the numerator to equal one, a patient
has to need mental or behavioral health supervision and has to have
these needs met by his or her caregiver, or could have their needs met
by the caregiver with additional training and/or support by the HHA.
The denominator is all episodes of care. The algorithm discussed
previously for HHA Correctly Identifies Patient's Need for Mental or
Behavioral Health Supervision could also be used to first identify if a
patient was in need of mental or behavioral health supervision.
To identify whether caregivers are able to provide supervisory care
or, with training, could be able to provide supervisory care for these
patients, we could use the SOC/ROC code for M2102f, Types and Sources
of Assistance: Supervision and Safety. If the HHA codes a value of 1
(Non-agency caregiver(s) currently provide assistance) or 2 (Non-agency
caregiver(s) need training/supportive services to provide assistance),
then the measure identifies that a caregiver does or could provide
supervision to a patient who has been identified as needing mental or
behavioral health supervision.
The outcome measure is defined as the agreement between the
algorithm's identification of a patient's need for mental or behavioral
health supervision and the availability of supervision from the
patient's caregiver(s). That is, if--
The algorithm identifies the patient as in need of mental
or behavioral health supervision and there is documentation that the
patient's caregiver(s) do or could provide this supervision; then
The outcome is coded as 1, successful.
As with other OASIS-based measures, a performance score for the
measure would only be calculated for HHAs that have 20 or more episodes
during a performance year. We would use the same methodology to risk-
adjust by using OASIS-C2 items and the prediction model described
previously. The prediction model for this outcome measure uses 55 risk
factors with each risk factor significant at p <0.0001. The correlation
for the model between observed and predicted values as estimated by
Somers' D is 0.672, that yields an estimated coefficient of
determination (r2) value based on the Tau-a of 0.205. This suggests
that the variability in the model accounts for (predicts) approximately
20 percent of the variability in the outcome measure. The best
statistic for evaluating the power of a prediction model that is
derived using logistic regression is the c-statistic. This statistic
identifies the overall accuracy of prediction by comparing observed and
predicted value pairs to the proportion of the time that both predict
the outcome in the same direction with 0.500 being a coin-flip. The
prediction model has a c-statistic equal to 0.836, which is considered
to be extremely strong.
We noted in the CY 2018 HH PPS proposed rule that we are
considering whether the HHA Correctly Identifies Patient's Need for
Mental or Behavioral Health Supervision measure or the Caregiver Can/
Does Provide for Patient's Mental or Behavioral Health
[[Page 51711]]
Supervision Need measure would be most meaningful to include in the
Model. We also noted that we were considering the interactions between
the Home Health Grouping Model (HHGM) proposal on quality measures
discussed in section III. of the proposed rule and the HHVBP Model for
the quality measures discussed in section IV.B of the proposed rule. We
solicited public comments on the methodologies, analyses used to test
the quality measure, and issues described in this section for future
measure considerations. We noted that we will continue to share
analyses as they become available with participating HHAs during future
webinars.
The following is a summary of the public comments received on the
``Quality Measures for Future Consideration'' and our responses:
Comment: We received several comments from stakeholders offering
their input on the quality measures discussed. Many were receptive to
the development of new measures. Some commenters supported the
development of composite measures, but believed improvement should not
be the sole focus of any measure as they indicated that many patients
benefit greatly from skilled home health services but are not likely to
improve on these measures. While many commenters were in support of the
inclusion of measures that capture an agency's ability to identify
mental or behavioral health needs and identify whether a caregiver is
available to provide behavioral supervision, they cautioned CMS that
home health providers should not be made responsible for determining
behavioral health diagnoses outside of a simple recognition of need.
MedPAC was one of a few commenters that did not support developing new
process measures, such as the described measure concepts of correctly
identifying the patient's need for mental and behavioral health
supervision, and identifying if a caregiver is able to provide the
patient's mental or behavioral health supervision. MedPAC indicated
that while it believes that improving a patient's functional ability is
a goal of home health care, it has some degree of concern that the
`composite total change in ADL/IADL measure' and the `composite
functional decline measure' represent reporting elements completely
within the control of the home health agency. MedPAC recommended that
if CMS includes these measures, it may also want to consider and
propose ways that such data could be independently audited or otherwise
verified. Another commenter opposed the addition of a composite
functional decline measure as they believe it rewards agencies that
have selective admission practices of refusing patients that are likely
to decline toward end of life, and also opposed the inclusion of
behavioral health measures as they believe that they may discourage
agencies from accepting patients when there are behavioral health
issues or few local resources.
Response: We appreciate the comments on the discussion of the
measures that we are considering for possible inclusion in the Model
and will take the recommendations into consideration as we determine
whether or not to include new measures in future rulemaking.
Comment: In response to our solicitation of public comment, we also
received a few comments that were outside the scope of discussion of
the specific future quality measures that we are considering, as
discussed in the proposed rule. A commenter recommended that CMS
develop and implement HHVBP policies in alignment with Congressional
activity supporting one national approach to VBP for home care
services. Another commenter recommended that CMS factor quality metrics
into HHVBP that not only relate to health outcomes, but also that are
within the control of the home health care provider, adequately
measuring the quality of care provided. Another commenter recommended
that CMS ensure that value-based home health purchasing models
incorporate a shared definition of value that incorporates the patient
and caregiver voice. A few commenters questioned the level of payment
at risk under the Model, and believed that placing up to eight percent
of HHA payment at risk for performance is too much. A few commenters
questioned the geographic participation criteria for the Model and
recommended including voluntary participation by interested HHAs in
non-participating states.
Response: We appreciate the comment to align home health VBP
policies with Congressional activity supporting a national approach to
VBP home care services. We also appreciate the comments that recommend
adequately measuring the quality of care provided and for CMS to ensure
that value-based home health purchasing models incorporate a shared
definition of value that incorporates the patient and caregiver voice.
As an Innovation Center model, we are closely monitoring the quality
measures and will address any needed adjustments through future
rulemaking. With respect to the comments regarding the level of payment
at risk under the Model, as discussed in the CY 2016 HH PPS final rule
(80 FR 68687), competing HHAs that provide the highest quality of care
and that receive the maximum upward adjustment will improve their
financial viability that could ensure that the vulnerable population
that they serve has access to high quality care. Only HHAs that provide
very poor quality of care, relative to the cohort they compete within,
would be subject to the highest downward payment adjustments. We
appreciate the desire for interested HHAs in non-participating states
to participate in the Model, but do not plan to re-open the Model to
additional participants at this time.
We appreciate the comments on potential new quality measures and
intend to continue to provide opportunities for stakeholder input as we
consider additional measures for possible inclusion in the HHVBP
Model's applicable measure set. We will continue to collect and analyze
data as we consider whether to propose any additional measures in
future rulemaking.
V. Updates to the Home Health Care Quality Reporting Program (HH QRP)
A. Background and Statutory Authority
Section 1895(b)(3)(B)(v)(II) of the Act requires that for 2007 and
subsequent years, each HHA submit to the Secretary in a form and
manner, and at a time, specified by the Secretary, such data that the
Secretary determines are appropriate for the measurement of health care
quality. To the extent that an HHA does not submit data in accordance
with this clause, the Secretary is directed to reduce the home health
market basket percentage increase applicable to the HHA for such year
by 2 percentage points. As provided at section 1895(b)(3)(B)(vi) of the
Act, depending on the market basket percentage increase applicable for
a particular year, the reduction of that increase by 2 percentage
points for failure to comply with the requirements of the HH QRP and
(except in 2018) further reduction of the increase by the productivity
adjustment described in section 1886(b)(3)(B)(xi)(II) of the Act may
result in the home health market basket percentage increase being less
than 0.0 percent for a year, and may result in payment rates under the
Home Health PPS for a year being less than payment rates for the
preceding year.
We use the terminology ``CY [year] HH QRP'' to refer to the
calendar year for which the HH QRP requirements applicable to that
calendar year must be met in order for an HHA to avoid a 2 percentage
point reduction to its market
[[Page 51712]]
basket percentage increase under section 1895(b)(3)(B)(v)(I) of the Act
when calculating the payment rates applicable to it for that calendar
year.
The Improving Medicare Post-Acute Care Transformation Act of 2014
(Pub. L. 113-185, enacted on October 6, 2014) (IMPACT Act) amended
Title XVIII of the Act, in part, by adding new section 1899B of the
Act, entitled ``Standardized Post-Acute Care Assessment Data for
Quality, Payment, and Discharge Planning,'' and by enacting new data
reporting requirements for certain post-acute care (PAC) providers,
including Home Health Agencies (HHAs). Specifically, new sections
1899B(a)(1)(A)(ii) and (iii) of the Act require HHAs, Inpatient
Rehabilitation Facilities (IRFs), Long Term Care Hospitals (LTCHs) and
Skilled Nursing Facilities (SNFs), under each of their respective
quality reporting program (which, for HHAs, is found at section
1895(b)(3)(B)(v) of the Act), to report data on quality measures
specified under section 1899B(c)(1) of the Act for at least five
domains, and data on resource use and other measures specified under
section 1899B(d)(1) of the Act for at least three domains. Section
1899B(a)(1)(A)(i) of the Act further requires each of these PAC
providers to report under its respective quality reporting program
standardized patient assessment data in accordance with subsection (b)
for at least the quality measures specified under subsection (c)(1) and
that is with respect to five specific categories: Functional status;
cognitive function and mental status; special services, treatments, and
interventions; medical conditions and co-morbidities; and impairments.
All of the data that must be reported in accordance with section
1899B(a)(1)(A) of the Act must be standardized and interoperable, so as
to allow for the exchange of the information among PAC providers and
other providers, as well as for the use of such data to enable access
to longitudinal information and to facilitate coordinated care. We
refer readers to the CY 2016 HH PPS final rule (80 FR 68690 through
68692) for additional information on the IMPACT Act and its
applicability to HHAs.
B. General Considerations Used for the Selection of Quality Measures
for the HH QRP
We refer readers to the CY 2016 HH PPS final rule (80 FR 68695
through 68698) for a detailed discussion of the considerations we apply
in measure selection for the HH QRP, such as alignment with the CMS
Quality Strategy,\24\ which incorporates the three broad aims of the
National Quality Strategy.\25\ As part of our consideration for
measures for use in the HH QRP, we review and evaluate measures that
have been implemented in other programs and take into account measures
that have been endorsed by NQF for provider settings other than the
home health setting. We have previously adopted measures with the term
``Application of'' in the names of those measures. We have received
questions pertaining to the term ``application'' and clarified in the
proposed rule that when we refer to a measure as an ``Application of''
the measure, we mean that the measure would be used in a setting other
than the setting for which it was endorsed by the NQF. For example, in
the FY 2016 SNF PPS Rule (80 FR 46440 through 46444) we adopted An
Application of the Measure Percent of Residents with Experiencing Falls
with Major Injury (Long Stay) (NQF #0674), which is endorsed for the
Nursing Home setting but not the SNF setting. For such measures, we
stated that we intend to seek NQF endorsement for the home health
setting, and if the NQF endorses one or more of them, we would update
the title of the measure to remove the reference to ``Application of.''
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\24\ https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/QualityInitiativesGenInfo/CMS-Quality-Strategy.html.
\25\ https://www.ahrq.gov/workingforquality/nqs/nqs2011annlrpt.htm.
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We received comments on the considerations we apply in our measure
selection and on other topics related to measures used in the HH QRP.
Comment: Some commenters supported the standardization of measures
and data across HHAs, LTCHs, IRFs, and SNFs so that CMS can make
comparisons between them, but cautioned that such standardization could
compromise the validity of the data. These commenters stated that the
home is different than institutional settings because the patient has a
greater role in determining how, when, and if certain interventions are
provided, and that individual skill, cognitive and functional ability,
and financial resources affect the ability of home health patients to
safely manage their health care needs, interventions, and medication
regimens. Other commenters expressed concerns about the reliability and
validity of cross-setting measures due to the unique characteristics of
the home health setting and emphasized caution in interpreting measure
rates.
Response: We appreciate the support for standardization to enable
comparisons across post-acute care providers. We also recognize the
uniqueness of the home setting, including patients' capacity to
directly and independently manage their environment and health care
needs, such as medications and treatments. However, we disagree that
patients are limited in their freedom to help set their goals and
preferences when receiving care services within LTCHs, IRFs or SNFs. In
our measure development and alignment work, we continuously assess and
account for the unique characteristics of home health patients
including the use of risk-adjustment models that account for
differences in cognitive and functional ability. Further, we are
mindful that regardless of where services are rendered, risk adjustment
is generally applied to characteristics of the individual rather than
the provider setting.
All of the measures we proposed to adopt for the HH QRP were tested
for reliability and/or validity, and we believe that the results of
that testing support our conclusion that the measures are sufficiently
reliable and valid to warrant their adoption in the HH QRP. The results
of our reliability and validity testing for these measures may be found
in the Measure Specifications for Measures Proposed in CY 2018 HH QRP
Final Rule, posted on the CMS HH QRP Web page at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html. We will continue to
test, monitor and validate these measures as part of measure
maintenance.
Comment: One commenter suggested that the claims-based measures be
weighted more than OASIS measures in order to control for inflated
outcomes. Another commenter was concerned that OASIS measure data can
be manipulated and suggested the HH QRP should only use claims-based
measures because they are more objective.
Response: We wish to clarify that we do not weight home health
measures in the home health quality reporting program. However, we
believe that the commenter is concerned about the gaming on behalf of
home health agencies. We believe that the collection of both claims-
based and OASIS based measures is appropriate for the program. Claims-
based data can be limited because they are associated with billing and
do not always provide a complete picture of the patient's health
assessment status. OASIS fills in those gaps by giving us additional
information about care processes and outcomes that are furnished to HHA
patients.
[[Page 51713]]
Although we recognize that OASIS assessments are, by their nature, more
subjective than claims, we require HHAs to attest to the accuracy of
the data submitted on each OASIS assessment.
C. Accounting for Social Risk Factors in the HH QRP
In the CY 2018 HH PPS proposed rule (82 FR 35341 through 35342), we
discussed accounting for social risk factors in the HH QRP. We
understand that social risk factors such as income, education, race and
ethnicity, employment, disability, community resources, and social
support (certain factors of which are also sometimes referred to as
socioeconomic status (SES) factors or socio-demographic status (SDS)
factors) play a major role in health. One of our core objectives is to
improve beneficiary outcomes including reducing health disparities, and
we want to ensure that all beneficiaries, including those with social
risk factors, receive high quality care. In addition, we seek to ensure
that the quality of care furnished by providers and suppliers is
assessed as fairly as possible under our programs while ensuring that
beneficiaries have adequate access to excellent care.
We have been reviewing reports prepared by the Office of the
Assistant Secretary for Planning and Evaluation (ASPE \26\) and the
National Academies of Sciences, Engineering, and Medicine on the issue
of measuring and accounting for social risk factors in CMS' quality
measurement and payment programs, and considering options on how to
address the issue in these programs. On December 21, 2016, ASPE
submitted a Report to Congress on a study it was required to conduct
under section 2(d) of the Improving Medicare Post-Acute Care
Transformation (IMPACT) Act of 2014. The study analyzed the effects of
certain social risk factors of Medicare beneficiaries on quality
measures and measures of resource use used in one or more of nine
Medicare value-based purchasing programs.\27\ The report also included
considerations for strategies to account for social risk factors in
these programs. In a January 10, 2017 report released by The National
Academies of Sciences, Engineering, and Medicine, that body provided
various potential methods for measuring and accounting for social risk
factors, including stratified public reporting.\28\
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\26\ https://aspe.hhs.gov/pdf-report/report-congress-social-risk-factors-and-performance-under-medicares-value-based-purchasing-programs.
\27\ https://aspe.hhs.gov/pdf-report/report-congress-social-risk-factors-and-performance-under-medicares-value-based-purchasing-programs.
\28\ National Academies of Sciences, Engineering, and Medicine.
2017. Accounting for social risk factors in Medicare payment.
Washington, DC: The National Academies Press.
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In addition, the NQF undertook a 2-year trial period in which new
measures, measures undergoing maintenance review, and measures endorsed
with the condition that they enter the trial period were assessed to
determine whether risk adjustment for selected social risk factors was
appropriate for these measures. Measures from the HH QRP,
Rehospitalization During the First 30 Days of Home Health (NQF# 2380),
and Emergency Department Use without Hospital Readmission During the
First 30 Days of Home Health (NQF# 2505) were included in this trial.
This trial entailed temporarily allowing inclusion of social risk
factors in the risk-adjustment approach for these measures. Since the
publication of the CY 2018 HH PPS proposed rule, the National Quality
Forum (NQF) has concluded their initial trial on risk adjustment for
quality measures. Based on the findings from the initial trial, NQF
will continue its work to evaluate the impact of social risk factor
adjustment on intermediate outcome and outcome measures for an
additional 3 years. The extension of this work will allow NQF to
determine further how to effectively account for social risk factors
through risk adjustment and other strategies in quality measurement.
As we continue to consider the analyses and recommendations from
these reports, we are continuing to work with stakeholders in this
process. As we have previously communicated, we are concerned about
holding providers to different standards for the outcomes of their
patients with social risk factors because we do not want to mask
potential disparities or minimize incentives to improve the outcomes
for disadvantaged populations. Keeping this concern in mind, while we
sought input on this topic previously, we continue to seek public
comment on whether we should account for social risk factors in
measures in the HH QRP, and if so, what method or combination of
methods would be most appropriate for accounting for social risk
factors. Examples of methods include: confidential reporting to
providers of measure rates stratified by social risk factors, public
reporting of stratified measure rates, and potential risk adjustment of
a particular measure as appropriate based on data and evidence.
In addition, in the CY 2018 HH PPS proposed rule (82 FR 35341
through 35342), we sought public comment on which social risk factors
might be most appropriate for reporting stratified measure scores and
potential risk adjustment of a particular measure. Examples of social
risk factors include, but are not limited to, dual eligibility/low-
income subsidy, race and ethnicity, and geographic area of residence.
We also sought comments on which of these factors, including current
data sources where this information would be available, could be used
alone or in combination, and whether other data should be collected to
better capture the effects of social risk. We will take commenters'
input into consideration as we continue to assess the appropriateness
and feasibility of accounting for social risk factors in the HH QRP. We
note that to the extent we consider making any changes we would propose
them through future notice and comment rulemaking.
We look forward to working with stakeholders as we consider the
issue of accounting for social risk factors and reducing health
disparities in CMS programs. Of note, implementing any of the methods
previously stated will be taken into consideration in the context of
how this and other CMS programs operate (for example, data submission
methods, availability of data, statistical considerations relating to
reliability of data calculations, among others), so we also sought
comment on operational considerations. We are committed to ensuring
that beneficiaries have access to and receive excellent care, and that
the quality of care furnished by providers and suppliers is assessed
fairly in CMS programs. This section of this final rule includes a
discussion of the comments we received on this topic, along with our
responses.
Comment: Commenters were generally supportive of accounting for
social risk factors in the HH QRP quality measures. Many commenters
stated that there was evidence demonstrating that these factors can
have substantial influence on patient health outcomes. Some commenters
who supported accounting for social risk factors noted that these
factors are outside the control of the provider and were concerned that
without risk adjustment, differences in quality scores may reflect
differences in patient populations rather than differences in quality.
A few other commenters, while acknowledging the influence of social
risk factors on health outcomes, cautioned against adjusting for them
in quality measurement due to the potential for unintended
consequences.
[[Page 51714]]
These commenters expressed concern over the possibility that risk-
adjusted measures may remove incentives for quality improvement among
facilities that serve higher levels of underserved populations.
Regarding risk adjustment methodology, some commenters made
specific recommendations regarding the type of risk adjustment that
must be used. Commenters stated that any risk stratification must be
considered on a measure-by-measure basis, and that measures that are
broadly within the control of the provider and reflective of direct
care, such as pressure ulcers, must not be stratified. The commenters
stated that social risk factor adjustment be used only on outcome
measures, not process measures. One commenter alternately suggested
using socioeconomic factors to stratify, rather than adjust, measure
results. Multiple commenters recommended that we conduct further
research and testing of risk-adjustment methods. A commenter suggested
that CMS use Social Risk Factors, Social Determinants of Health or
Distressed Communities Index scores within the HH QRP. Some commenters
suggested the formation of a TEP to further refine the use of such
data.
In addition to supporting race and ethnicity, dual eligibility
status, and geographical location, commenters suggested additional risk
factors, including: Patient-level factors such as lack of personal
resources, education level, and employment. Some commenters also
suggested community resources and other factors such as access to
adequate food, medications, living conditions (including living alone),
and lack of an adequate support system or caregiver availability.
Several encouraged the development of measures that reflect person-
centered domains to improve the focus on outcomes for disadvantaged
populations.
A few commenters provided feedback on confidential and public
reporting of data adjusted for social risk factors. A commenter
suggested that CMS start with confidential reporting and, once there
has been opportunity for HHAs to review and understand their results,
CMS could transition to public reporting.
Response: We thank commenters for their suggestions. As we have
previously stated, we are concerned about holding providers to
different standards for the outcomes of their patients with social risk
factors because we do not want to mask potential disparities. We
believe that the path forward must incentivize improvements in health
outcomes for disadvantaged populations while ensuring that
beneficiaries have adequate access to excellent care. Also, based on
the findings from the initial trial, NQF will continue its work to
evaluate the impact of social risk factor adjustment on intermediate
outcome and outcome measures for an additional three years. The
extension of this work will allow NQF to determine further how to
effectively account for social risk factors through risk adjustment and
other strategies in quality measurement. We await recommendations of
the NQF trial to further inform our efforts.
We will consider all suggestions as we continue to assess each
measure and the overall HH QRP. We intend to explore options including
but not limited to measure stratification by social risk factors in a
consistent manner across several quality reporting programs, informed
by considerations of stratification methods described in IX.A.13 of the
preamble of the FY 2018 IPPS/LTCH PPS final rule. We thank commenters
for this important feedback and will continue to consider options to
account for social risk factors that will allow us to address
disparities and potentially incentivize improvement in care for
patients and beneficiaries. We will also consider providing feedback to
providers on outcomes for individuals with social risk factors in
confidential reports.
D. Removal of OASIS Items
In the CY 2018 HH PPS proposed rule (82 FR 35342) we proposed to
remove 247 data elements from 35 OASIS items collected at specific time
points during a home health episode. These data elements are not used
in the calculation of quality measures already adopted in the HH QRP,
nor are they being used for previously established purposes unrelated
to the HH QRP, including payment, survey, the HH VBP Model or care
planning. We included list of the 35 OASIS items we proposed to remove,
in part or in their entirety, in Table 45 of the proposed rule (82 FR
35342 and 35343) and also made them available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/OASIS-Data-Sets.html. Subsequent to issuing the
proposed rule, we discovered that we had inadvertently included three
OASIS items in Table 45 that are used either for payment or for the HH
QRP. Those items are M1200 Vision (used for payment), M2030 Management
of Injectable Medications (used for payment), and M1730 Depression
Screening (used in the HH QRP). Accordingly, we will not be removing
these items from the OASIS.
Comment: Many commenters supported our proposal to remove items
from OASIS. Most of these commenters agreed that items not used for the
purposes of determining patient outcomes or the quality of care should
be removed.
Response: We appreciate the support for our proposal to remove
items from OASIS.
Comment: One commenter noted that OASIS Item M2250 (Plan of Care
Synopsis) is proposed for removal and questioned whether OASIS Item
M2401 (Intervention Synopsis) will continue to be collected.
Response: We proposed to remove OASIS Item M2250 because it is not
used for the HH QRP or for any other purpose. OASIS Item M2401 is used
in the calculation of the quality measure Diabetic Foot Care and
Patient Education Implemented (NQF #0519), which we adopted in the CY
2010 HH PPS final rule (74 FR 58096), and will therefore continue to be
collected at the time point of Transfer to an Inpatient Facility and
Discharge from Agency.
Comment: One commenter questioned if there is another OASIS version
that will be implemented so that a beneficiary's Medicare Beneficiary
Identifier (MBI) can be provided in the OASIS.
Response: Effective January 1, 2018 the OASIS-C2 will be able to
accommodate the MBI which is an alternative Medicare Beneficiary
Identifier that we are adopting to replace the Social Security number
(SSN)-based Health Insurance Claim Number (HICN) in an effort to
prevent identity theft in the Medicare population. Instructions for
reporting OASIS Item M0063 (Medicare Beneficiary Number) can be found
in the OASIS-C2 Guidance Manual: Effective January 1, 2018 at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/Downloads/OASIS-C2-Guidance-Manual-Effective_1_1_18.pdf.
Comment: A few commenters raised concerns about the overall burden
associated with CMS' proposals, noting that if all proposed new
assessment items are finalized, the new assessment items could be more
burdensome to collect than the one being removed.
Response: We appreciate the comments and as more fully discussed in
section V.H. of this final rule, we have decided not to finalize the
standardized patient assessment data elements proposed for three of the
five categories under Sec. 1899B(b)(1)(B) of the Act: Cognitive
Function and Mental
[[Page 51715]]
Status; Special Services, Treatments, and Interventions; and
Impairments.
Final Decision: After consideration of the comments received, we
are finalizing the removal of 235 data elements from 33 OASIS items
collected at specific time points during a home health episode,
effective with all HHA assessments on or after January 1, 2019. As
previously explained, we will continue to collect OASIS items M1200,
M2030 and M1730. Table 17 lists the OASIS items and data elements to be
removed and they can also be found at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/OASIS-Data-Sets.html.
Table 17--Items To Be Removed From OASIS Effective January 1, 2019
--------------------------------------------------------------------------------------------------------------------------------------------------------
Specific time point
-----------------------------------------------------------------------------------------------
OASIS item Transfer to an
Start of care Resumption of Follow-up inpatient Death at home Discharge from
care facility agency
--------------------------------------------------------------------------------------------------------------------------------------------------------
M0903................................................... .............. .............. .............. 1 1 1
M1011................................................... 6 6 6 .............. .............. ..............
M1017................................................... 6 6 .............. .............. .............. ..............
M1018................................................... 6 6 .............. .............. .............. ..............
M1025................................................... 12 12 12 .............. .............. ..............
M1034................................................... 1 1 .............. .............. .............. ..............
M1036................................................... 4 4 .............. .............. .............. ..............
M1210................................................... 1 1 .............. .............. .............. ..............
M1220................................................... 1 1 .............. .............. .............. ..............
M1230................................................... 1 1 .............. .............. .............. 1
M1240................................................... 1 1 .............. .............. .............. ..............
M1300................................................... 1 1 .............. .............. .............. ..............
M1302................................................... 1 1 .............. .............. .............. ..............
M1320................................................... 1 1 .............. .............. .............. 1
M1322................................................... .............. .............. .............. .............. .............. 1
M1332................................................... .............. .............. .............. .............. .............. 1
M1350................................................... 1 1 .............. .............. .............. ..............
M1410................................................... 3 3 .............. .............. .............. ..............
M1501................................................... .............. .............. .............. 1 .............. 1
M1511................................................... .............. .............. .............. 5 .............. 5
M1610................................................... .............. .............. .............. .............. .............. 1
M1615................................................... 1 1 .............. .............. .............. 1
M1750................................................... 1 1 .............. .............. .............. ..............
M1880................................................... 1 1 .............. .............. .............. 1
M1890................................................... 1 1 .............. .............. .............. 1
M1900................................................... 4 4 .............. .............. .............. ..............
M2030................................................... .............. .............. .............. .............. .............. 1
M2040................................................... 2 2 .............. .............. .............. ..............
M2102 *................................................. 6 6 .............. .............. .............. ** 3
M2110................................................... 1 1 .............. .............. .............. ..............
M2250................................................... 7 7 .............. .............. .............. ..............
M2310................................................... .............. .............. .............. *** 15 .............. *** 15
M2430................................................... .............. .............. .............. 20 .............. ..............
-----------------------------------------------------------------------------------------------
Total............................................... 70 70 18 42 1 34
--------------------------------------------------------------------------------------------------------------------------------------------------------
* M2102 row f to remain collected at Start of Care, Resumption of Care and Discharge from Agency as part of the HH VBP program.
** M2102 rows a, c, d to remain collected at Discharge from Agency for survey purposes.
*** M2310 responses 1, 10, OTH, UK to remain collected at Transfer to an Inpatient Facility and Discharge from Agency for survey purposes.
E. Collection of Standardized Patient Assessment Data Under the HH QRP
1. Definition of Standardized Patient Assessment Data
Section 1895(b)(3)(B)(v)(IV)(bb) of the Act requires that beginning
with the CY 2019 HH QRP, HHAs report standardized patient assessment
data required under section 1899B(b)(1) of the Act. For purposes of
meeting this requirement, section 1895(b)(3)(B)(v)(IV)(cc) of the Act
requires that a HHA submit the standardized patient assessment data
required under section 1899B(b)(1) of the Act in the form and manner,
and at the time, as specified by the Secretary.
Section 1899B(b)(1)(B) of the Act describes standardized patient
assessment data as data required for at least the quality measures
described in sections 1899B(c)(1) of the Act and that is with respect
to the following categories:
Functional status, such as mobility and self-care at
admission to a PAC provider and before discharge from a PAC provider.
Cognitive function, such as ability to express and
understand ideas, and mental status, such as depression and dementia.
Special services, treatments and interventions such as the
need for ventilator use, dialysis, chemotherapy, central line
placement, and total parenteral nutrition.
Medical conditions and comorbidities such as diabetes,
congestive heart failure and pressure ulcers.
Impairments, such as incontinence and an impaired ability
to hear, see or swallow.
Other categories deemed necessary and appropriate by the
Secretary.
As required under section 1899B(b)(1)(A) of the Act, the
standardized patient assessment data must be reported at least for the
beginning of the home health episode (for example, HH start of care/
resumption of care) and end of episode
[[Page 51716]]
(discharge), but the Secretary may require the data to be reported more
frequently.
In the CY 2018 HH PPS proposed rule (82 FR 35343), we proposed to
define the standardized patient assessment data that HHAs must report
under the HH QRP, as well as the requirements for the reporting of
these data. The collection of standardized patient assessment data is
critical to our efforts to drive improvement in healthcare quality
across the four post-acute care (PAC) settings to which the IMPACT Act
applies. We noted that we intend to use these data for a number of
purposes, including facilitating their exchange and longitudinal use
among healthcare providers to enable high quality care and outcomes
through care coordination, as well as for quality measure calculation,
and identifying comorbidities that might increase the medical
complexity of a particular admission.
HHAs are currently required to report patient assessment data
through the Outcome and Assessment Information Set (OASIS) by
responding to an identical set of assessment questions using an
identical set of response options (we refer to a solitary question/
response option as a data element and we refer to a group of questions/
responses as data elements), both of which incorporate an identical set
of definitions and standards. The primary purpose of the identical
questions and response options is to ensure that we collect a set of
standardized data elements across HHAs, which we can then use for a
number of purposes, including HH payment and measure calculation for
the HH QRP.
LTCHs, IRFs, and SNFs are also required to report patient
assessment data through their applicable PAC assessment instruments,
and they do so by responding to identical assessment questions
developed for their respective settings using an identical set of
response options (which incorporate an identical set of definitions and
standards). Like the OASIS, the questions and response options for each
of these other PAC assessment instruments are standardized across the
PAC provider type to which the PAC assessment instrument applies.
However, the assessment questions and response options in the four PAC
assessment instruments are not currently standardized with each other.
As a result, questions and response options that appear on the OASIS
cannot be readily compared with questions and response options that
appear, for example, on the Inpatient Rehabilitation Facility-Patient
Assessment Instrument (IRF-PAI), which is the PAC assessment instrument
used by IRFs. This is true even when the questions and response options
are similar. This lack of standardization across the four PAC provider
types has limited our ability to compare one PAC provider type with
another for purposes such as care coordination and quality improvement.
To achieve a level of standardization across HHAs, LTCHs, IRFs, and
SNFs that enables us to make comparisons between them, we proposed to
define ``standardized patient assessment data'' as patient or resident
assessment questions and response options that are identical in all
four PAC assessment instruments, and to which identical standards and
definitions apply.
We stated in the proposed rule that standardizing the questions and
response options across the four PAC assessment instruments is an
essential step in making that data interoperable, allowing it to be
shared electronically, or otherwise, between PAC provider types. It
will enable the data to be comparable for various purposes, including
the development of cross-setting quality measures and to inform payment
models that take into account patient characteristics rather than
setting, as described in the IMPACT Act.
We did not receive any specific comments on the proposed
definition.
Final Decision: We are finalizing as proposed our definition of
standardized patient assessment data.
2. General Considerations Used for the Selection of Standardized
Patient Assessment Data
As part of our effort to identify appropriate standardized patient
assessment data for purposes of collecting under the HH QRP, we sought
input from the general public, stakeholder community, and subject
matter experts on items that would enable person-centered, high quality
health care, as well as access to longitudinal information to
facilitate coordinated care and improved beneficiary outcomes.
To identify optimal data elements for standardization, our data
element contractor organized teams of researchers for each category,
with each team working with a group of advisors made up of clinicians
and academic researchers with expertise in PAC. Information-gathering
activities were used to identify data elements, as well as key themes
related to the categories described in section 1899B(b)(1)(B) of the
Act. In January and February 2016, our data element contractor also
conducted provider focus groups for each of the four PAC provider
types, and a focus group for consumers that included current or former
PAC patients and residents, caregivers, ombudsmen, and patient advocacy
group representatives. The Development and Maintenance of Post-Acute
Care Cross-Setting Standardized Patient Assessment Data Focus Group
Summary Report is available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/IMPACT-Act-of-2014/IMPACT-Act-Downloads-and-Videos.html.
Our data element contractor also assembled a 16-member TEP that met
on April 7 and 8, 2016, and January 5 and 6, 2017, in Baltimore,
Maryland, to provide expert input on data elements that are currently
in each PAC assessment instrument, as well as data elements that could
be standardized. The Development and Maintenance of Post-Acute Care
Cross-Setting Standardized Patient Assessment Data TEP Summary Reports
are available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/IMPACT-Act-of-2014/IMPACT-Act-Downloads-and-Videos.html.
As part of the environmental scan, data elements currently in the
four existing PAC assessment instruments were examined to see if any
could be considered for proposal as standardized patient assessment
data. Specifically, this evaluation included consideration of data
elements in OASIS-C2 (effective January 2017); IRF-PAI, v1.4 (effective
October 2016); LCDS, v3.00 (effective April 2016); and MDS 3.0, v1.14
(effective October 2016). Data elements in the standardized assessment
instrument that we tested in the Post-Acute Care Payment Reform
Demonstration (PAC PRD)--the Continuity Assessment Record and public
reporting Evaluation (CARE)--were also considered. A literature search
was also conducted to determine whether we could propose to adopt
additional data elements as standardized patient assessment data.
Additionally, we held four Special Open Door Forums (SODFs) on
October 27, 2015; May 12, 2016; September 15, 2016; and December 8,
2016, to present data elements we were considering and to solicit
input. At each SODF, some stakeholders provided immediate input, and
all were invited to submit additional comments via the CMS IMPACT
Mailbox: PACQualityInitiative@cms.hhs.gov.
[[Page 51717]]
We also convened a meeting with federal agency subject matter
experts (SMEs) on May 13, 2016. In addition, a public comment period
was open from August 12 to September 12, 2016 to solicit comments on
detailed candidate data element descriptions, data collection methods,
and coding methods. The IMPACT Act Public Comment Summary Report
containing the public comments (summarized and verbatim) and our
responses is available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/IMPACT-Act-of-2014/IMPACT-Act-Downloads-and-Videos.html.
We specifically sought to identify standardized patient assessment
data that we could feasibly incorporate into the LTCH, IRF, SNF, and
HHA assessment instruments and that have the following attributes: (1)
Being supported by current science; (2) testing well in terms of their
reliability and validity, consistent with findings from the Post-Acute
Care Payment Reform Demonstration (PAC PRD); (3) the potential to be
shared (for example, through interoperable means) among PAC and other
provider types to facilitate efficient care coordination and improved
beneficiary outcomes; (4) the potential to inform the development of
quality, resource use and other measures, as well as future payment
methodologies that could more directly take into account individual
beneficiary health characteristics; and (5) the ability to be used by
practitioners to inform their clinical decision and care planning
activities. We also applied the same considerations that we apply to
quality measures, including the CMS Quality Strategy which is framed
using the three broad aims of the National Quality Strategy.
3. Policy for Retaining HH QRP Measures and Standardized Patient
Assessment Data
In the CY 2017 HH PPS final rule (81 FR 76755 through 76756), we
adopted a policy that will allow for any quality measure adopted for
use in the HH QRP to remain in effect until the measure is removed,
suspended, or replaced. For further information on how measures are
considered for removal, suspension or replacement, we refer readers to
the CY 2017 HH PPS final rule (81 FR 76755 through 76756). We proposed
to apply this same policy to the standardized patient assessment data
that we adopt for the HH QRP.
Comment: Several commenters supported this proposal.
Response: We appreciate the commenters' support.
Final Decision: We are finalizing that our policy for retaining HH
QRP measures will apply to the standardized patient assessment data
that we adopt for the HH QRP.
4. Policy for Adopting Changes to HH QRP Measures and Application of
That Policy to Standardized Patient Assessment Data
In the CY 2017 HH PPS final rule (81 FR 76756), we adopted a
subregulatory process to incorporate updates to HH quality measure
specifications that do not substantively change the nature of the
measure. We noted that substantive changes will be proposed and
finalized through rulemaking. For further information on what
constitutes a substantive versus a nonsubstantive change and the
subregulatory process for nonsubstantive changes, we refer readers to
the CY 2017 HH PPS final rule (81 FR 76756). We proposed to apply this
policy to the standardized patient assessment data that we adopt for
the HH QRP. We invited public comment on this proposal.
Comment: One commenter requested that we propose to adopt all
substantive changes to measures only after soliciting input from a
technical expert panel of home health clinical leaders, holding a
Special Open Door Forum to explain the changes under consideration, and
allowing stakeholders to submit meaningful comments on those potential
changes.
Response: We agree that input from both technical experts and the
public is critical to the measure development process, and we generally
solicit both types of input when we consider whether to propose
substantive updates to measures. We also solicit input in other ways,
such as through open door forums and solicitations for public comment,
and often engage in these activities prior to proposing substantive
updates through the rulemaking process. Finally, the rulemaking process
itself gives the public an additional opportunity to comment on the
substantive updates to measures under consideration.
Final Decision: After consideration of the public comments, we are
finalizing that we will apply our policy for adopting changes to HH QRP
measures to the standardized patient assessment data that we adopt for
the HH QRP.
5. Quality Measures Previously Finalized for the HH QRP
The HH QRP currently has 23 measures, as outlined in Table 18.
Table 18--Measures Currently Adopted for the HH QRP
----------------------------------------------------------------------------------------------------------------
Short name Measure name & data source
----------------------------------------------------------------------------------------------------------------
OASIS-based
----------------------------------------------------------------------------------------------------------------
Pressure Ulcers........................................... Percent of Patients or Residents with Pressure
Ulcers that are New or Worsened (NQF # 0678).* +
DRR....................................................... Drug Regimen Review Conducted with Follow-Up for
Identified Issues-Post Acute Care (PAC) Home Health
Quality Reporting Program.+
Ambulation................................................ Improvement in Ambulation/Locomotion (NQF #0167).
Bathing................................................... Improvement in Bathing (NQF #0174).
Dyspnea................................................... Improvement in Dyspnea.
Oral Medications.......................................... Improvement in Management of Oral Medication (NQF
#0176).
Pain...................................................... Improvement in Pain Interfering with Activity (NQF
#0177).
Surgical Wounds........................................... Improvement in Status of Surgical Wounds (NQF
#0178).
Bed Transferring.......................................... Improvement in Bed Transferring (NQF # 0175).
Timely Care............................................... Timely Initiation Of Care (NQF # 0526).
Depression Assessment..................................... Depression Assessment Conducted.
Influenza................................................. Influenza Immunization Received for Current Flu
Season (NQF #0522).
PPV....................................................... Pneumococcal Polysaccharide Vaccine Ever Received
(NQF #0525).
Falls Risk................................................ Multifactor Fall Risk Assessment Conducted For All
Patients Who Can Ambulate (NQF #0537).
Diabetic Foot Care........................................ Diabetic Foot Care and Patient/Caregiver Education
Implemented during All Episodes of Care (NQF
#0519).
Drug Education............................................ Drug Education on All Medications Provided to
Patient/Caregiver during All Episodes of Care.
----------------------------------------------------------------------------------------------------------------
Claims-based
----------------------------------------------------------------------------------------------------------------
MSPB...................................................... Total Estimated Medicare Spending Per Beneficiary
(MSPB)--Post Acute Care (PAC) Home Health (HH)
Quality Reporting Program (QRP). +
[[Page 51718]]
DTC....................................................... Discharge to Community-Post Acute Care (PAC) Home
Health (HH) Quality Reporting Program (QRP). +
PPR....................................................... Potentially Preventable 30-Day Post-Discharge
Readmission Measure for Home Health Quality
Reporting Program. +
ACH....................................................... Acute Care Hospitalization During the First 60 Days
of Home Health (NQF #0171).
ED Use.................................................... Emergency Department Use without Hospitalization
During the First 60 Days of Home Health (NQF
#0173).
Rehospitalization......................................... Rehospitalization During the First 30 Days of Home
Health (NQF #2380).
ED Use without Readmission................................ Emergency Department Use without Hospital
Readmission During the First 30 Days of Home Health
(NQF #2505).
----------------------------------------------------------------------------------------------------------------
HHCAHPs-based
----------------------------------------------------------------------------------------------------------------
Professional Care......................................... How often the home health team gave care in a
professional way.
Communication............................................. How well did the home health team communicate with
patients.
Team Discussion........................................... Did the home health team discuss medicines, pain,
and home safety with patients.
Overall Rating............................................ How do patients rate the overall care from the home
health agency.
Willing to Recommend...................................... Will patients recommend the home health agency to
friends and family.
----------------------------------------------------------------------------------------------------------------
* Not currently NQF-endorsed for the home health setting.
The data collection period will begin with CY 2017 Q1&2 reporting for CY 2018 APU determination, followed by
the previously established HH QRP use of 12 months (July 1, 2017-June 30, 2018) of CY 2017 reporting for CY
2019 APU determination. Subsequent years will be based on the HH July 1-June 30 timeframe for APU purposes.
For claims data, the performance period will use rolling CY claims for subsequent reporting purposes.
F. New HH QRP Quality Measures Beginning With the CY 2020 HH QRP
In the CY 2018 HH PPS proposed rule (82 FR 35345) we proposed that
beginning with the CY 2020 HH QRP, in addition to the quality measures
we are retaining under our policy described in section V.B. of this
final rule, we would replace the current pressure ulcer measure
entitled Percent of Residents or Patients with Pressure Ulcers That Are
New or Worsened (Short Stay) (NQF #0678) with a modified version of the
measure and adopt one measure on patient falls and one measure on
assessment of patient functional status. We also proposed to
characterize the data elements described in this section as
standardized patient assessment data under section 1899B(b)(1)(B) of
the Act that must be reported by HHAs under the HH QRP through the
OASIS. The new measures that we proposed to adopt are as follows:
Changes in Skin Integrity Post-Acute Care: Pressure Ulcer/
Injury.
Application of Percent of Residents Experiencing One or
More Falls with Major Injury (NQF #0674).
Application of Percent of Long-Term Care Hospital Patients
with an Admission and Discharge Functional Assessment and a Care Plan
That Addresses Function (NQF #2631).
The measures are described in more detail as follows:
1. Replacing the Current Pressure Ulcer Quality Measure, Entitled
Percent of Residents or Patients With Pressure Ulcers That Are New or
Worsened (Short Stay) (NQF #0678), With a Modified Pressure Ulcer
Measure, Entitled Changes in Skin Integrity Post-Acute Care: Pressure
Ulcer/Injury
a. Measure Background
We proposed to remove the current pressure ulcer measure, Percent
of Residents or Patients with Pressure Ulcers That Are New or Worsened
(Short Stay) (NQF #0678), from the HH QRP measure set and to replace it
with a modified version of that measure, Changes in Skin Integrity
Post-Acute Care: Pressure Ulcer/Injury, beginning with the CY 2020 HH
QRP. The change in the measure name is to reduce confusion about the
new modified measure. The modified version differs from the current
version of the measure because it includes new or worsened unstageable
pressure ulcers, including deep tissue injuries (DTIs), in the measure
numerator. The proposed modified version of the measure also contained
updated specifications intended to eliminate redundancies in the
assessment items needed for its calculation and to reduce the potential
for underestimating the frequency of pressure ulcers. The modified
version of the measure would satisfy the IMPACT Act domain of ``Skin
integrity and changes in skin integrity.''
b. Measure Importance
As described in the CY 2016 HH PPS final rule (80 FR 68697),
pressure ulcers are high-cost adverse events and are an important
measure of quality. For information on the history and rationale for
the relevance, importance, and applicability of having a pressure ulcer
measure in the HH QRP, we referred readers to the CY 2016 HH PPS final
rule (80 FR 68697 to 68700.
We proposed to adopt a modified version of the current pressure
ulcer measure because unstageable pressure ulcers, including DTIs, are
similar to Stage 2, Stage 3, and Stage 4 pressure ulcers in that they
represent poor outcomes, are a serious medical condition that can
result in death and disability, are debilitating and painful and are
often an avoidable outcome of medical care.\29\ \30\ \31\ \32\ \33\
\34\ Studies show that most pressure ulcers can be avoided and can also
be healed in acute, post-acute, and long term care settings with
appropriate medical care. \35\ Furthermore, some studies indicate that
DTIs, if managed using appropriate care, can be resolved without
deteriorating into a worsened pressure ulcer.\36\ \37\
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\29\ Casey, G. (2013). ``Pressure ulcers reflect quality of
nursing care.'' Nurs N Z 19(10): 20-24.
\30\ Gorzoni, M.L. and S.L. Pires (2011). ``Deaths in nursing
homes.'' Rev Assoc Med Bras 57(3): 327-331.
\31\ Thomas, J.M., et al. (2013). ``Systematic review: health-
related characteristics of elderly hospitalized adults and nursing
home residents associated with short-term mortality.'' J Am Geriatr
Soc 61(6): 902-911.
\32\ White-Chu, E.F., et al. (2011). ``Pressure ulcers in long-
term care.'' Clin Geriatr Med 27(2): 241-258.
\33\ Bates-Jensen BM. Quality indicators for prevention and
management of pressure ulcers in vulnerable elders. Ann Int Med.
2001;135 (8 Part 2), 744-51.
\34\ Bennet, G, Dealy, C Posnett, J (2004). The cost of pressure
ulcers in the UK, Age and Aging, 33(3):230-235.
\35\ Black, Joyce M., et al. ``Pressure ulcers: avoidable or
unavoidable? Results of the national pressure ulcer advisory panel
consensus conference.'' Ostomy-Wound Management 57.2 (2011): 24.
\36\ Sullivan, R. (2013). A Two-year Retrospective Review of
Suspected Deep Tissue Injury Evolution in Adult Acute Care Patients.
Ostomy Wound Management 59(9) https://www.o-wm.com/article/two-year-retrospective-review-suspected-deep-tissue-injury-evolution-adult-acute-care-patien.
\37\ Posthauer, ME, Zulkowski, K. (2005). Special to OWM: The
NPUAP Dual Mission Conference: Reaching Consensus on Staging and
Deep Tissue Injury. Ostomy Wound Management 51(4) https://www.o-wm.com/content/the-npuap-dual-mission-conference-reaching-consensus-staging-and-deep-tissue-injury.
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While there are few studies that provide information regarding the
incidence of unstageable pressure ulcers in PAC settings, an analysis
conducted by our measure development contractor indicated that adding
unstageable pressure ulcers to the quality measure numerator would
result in a higher
[[Page 51719]]
percentage of patients with new or worsened pressure ulcers in HHA
settings and increase the variability of measure scores. A higher
percentage indicates lower quality. This increased variability serves
to improve the measure by improving the ability of the measure to
distinguish between high and low quality home health agencies.
We have found in the testing of this measure that given the low
prevalence of pressure ulcers in the home health setting, the addition
of unstageable ulcers to this measure could enhance variability.
Analysis of 2015 OASIS data found that in approximately 1.2 percent, or
more than 70,000 episodes, of patients had an unstageable ulcer upon
admission. Patients in more than 13,000 episodes were discharged with
an unstageable ulcer. In addition, unstageable ulcers due to slough/
eschar worsened between admission and discharge in approximately 5,000
episodes of care. In conclusion, the inclusion of unstageable pressure
ulcers, including DTIs, in the numerator of this measure is expected to
increase measure scores and variability in measure scores, thereby
improving the ability to discriminate among poor- and high-performing
HHAs.
Testing shows similar results in other PAC settings. For example,
in SNFs, using data from Quarter 4 2015 through Quarter 3 2016, the
mean score on the currently implemented pressure ulcer measure is 1.75
percent, compared with 2.58 percent in the proposed measure. In the
proposed measure, the SNF mean score is 2.58 percent; the 25th and 75th
percentiles are 0.65 percent and 3.70 percent, respectively; and 20.32
percent of facilities have perfect scores. In LTCHs, using data from
Quarter 1 through Quarter 4 2015, the mean score on the currently
implemented pressure ulcer measure is 1.95 percent, compared with 3.73
percent in the proposed measure. In the proposed measure, the LTCH mean
score is 3.73 percent; the 25th and 75th percentiles are 1.53 percent
and 4.89 percent, respectively; and 5.46 percent of facilities have
perfect scores. In IRFs, using data from Quarter 4 2016, the mean score
on the currently implemented pressure ulcer measure is 0.64 percent,
compared with 1.46 percent in the proposed measure. In the proposed
measure, the IRF mean score is 1.46 percent and the 25th and 75th
percentiles are 0 percent and 2.27 percent, respectively. The inclusion
of unstageable pressure ulcers, including DTIs, in the numerator of
this measure is expected to increase measure scores and variability in
measure scores, thereby improving the ability to distinguish between
poor and high performing HHAs.
This increased variability of scores across quarters and deciles
may improve the ability of the measure to distinguish between high and
low performing providers across PAC settings.
c. Stakeholder Feedback
Our measure development contractor sought input from subject matter
experts, including Technical Expert Panels (TEPs), over the course of
several years on various skin integrity topics and specifically those
associated with the inclusion of unstageable pressure ulcers including
DTIs. Most recently, on July 18, 2016, a TEP convened by our measure
development contractor provided input on the technical specifications
of this proposed quality measure, including the feasibility of
implementing the proposed measure's updates across PAC settings. The
TEP supported the use of the proposed measure across PAC settings,
including the use of different data elements for measure calculation.
The TEP supported the updates to the measure across PAC settings,
including the inclusion in the numerator of unstageable pressure ulcers
due to slough and/or eschar that are new or worsened, new unstageable
pressure ulcers due to a non-removable dressing or device, and new
DTIs. The TEP recommended supplying additional guidance to providers
regarding each type of unstageable pressure ulcer. This support was in
agreement with earlier TEP meetings, held on June 13, and November 15,
2013, which had recommended that CMS update the specifications for the
pressure ulcer measure to include unstageable pressure ulcers in the
numerator.\38\ \39\ Exploratory data analysis conducted by our measure
development contractor suggests that the addition of unstageable
pressure ulcers, including DTIs, will increase the observed incidence
of new or worsened pressure ulcers at the facility level and may
improve the ability of the proposed quality measure to discriminate
between poor- and high-performing agencies.
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\38\ Schwartz, M., Nguyen, K.H., Swinson Evans, T.M., Ignaczak,
M.K., Thaker, S., and Bernard, S.L.: Development of a Cross-Setting
Quality Measure for Pressure Ulcers: OY2 Information Gathering,
Final Report. Centers for Medicare & Medicaid Services, November
2013. Available: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/Downloads/Development-of-a-Cross-Setting-Quality-Measure-for-Pressure-Ulcers-Information-Gathering-Final-Report.pdf.
\39\ Schwartz, M., Ignaczak, M.K., Swinson Evans, T.M., Thaker,
S., and Smith, L.: The Development of a Cross-Setting Pressure Ulcer
Quality Measure: Summary Report on November 15, 2013, Technical
Expert Panel Follow-Up Webinar. Centers for Medicare & Medicaid
Services, January 2014. Available: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/Downloads/Development-of-a-Cross-Setting-Pressure-Ulcer-Quality-Measure-Summary-Report-on-November-15-2013-Technical-Expert-Pa.pdf.
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We solicited stakeholder feedback on this proposed measure by means
of a public comment period held from October 17 through November 17,
2016. In general, we received considerable support for the proposed
measure. A few commenters supported all of the changes to the current
pressure ulcer measure that resulted in the proposed measure, with one
commenter noting the significance of the work to align the pressure
ulcer quality measure specifications across the PAC settings. Many
commenters supported the inclusion of unstageable pressure ulcers due
to slough/eschar, due to non-removable dressing/device, and DTIs in the
proposed quality measure. Other commenters did not support the
inclusion of DTIs in the proposed quality measure because they stated
that there is no universally accepted definition for this type of skin
injury.
Some commenters provided feedback on the data elements used to
calculate the proposed quality measure. We believe that these data
elements will promote facilitation of cross-setting quality comparison
as required under the IMPACT Act, alignment between quality measures
and payment, reduction in redundancies in assessment items, and
prevention of inappropriate underestimation of pressure ulcers. The
currently implemented pressure ulcer measure is calculated using
retrospective data elements that assess the number of new or worsened
pressure ulcers at each stage, while the proposed measure is calculated
using data elements that assess the current number of unhealed pressure
ulcers at each stage, and the number of these that were present upon
admission, which are subtracted from the current number at that stage.
Some commenters did not support the data elements that will be used to
calculate the proposed measure, and requested further testing of these
data elements. Other commenters supported the use of these data
elements stating that these data elements simplified the measure
calculation process.
The public comment summary report for the proposed measure is
available on the CMS Web site at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/IMPACT-Act-of-2014/IMPACT-Act-Downloads-and-Videos.html.
[[Page 51720]]
The NQF-convened Measures Application Partnership (MAP) Post-Acute
Care/Long-Term Care (PAC/LTC) Workgroup met on December 14 and 15,
2016, and provided us input about this proposed measure. The NQF-
convened MAP PAC/LTC workgroup provided a recommendation of ``support
for rulemaking'' for use of the proposed measure in the HH QRP. The MAP
Coordinating Committee met on January 24 and 25, 2017, and provided a
recommendation of ``conditional support for rulemaking'' for use of the
proposed measure in the HH QRP. The MAP's conditions of support include
that, as a part of measure implementation, we provide guidance on the
correct collection and calculation of the measure result, as well as
guidance on public reporting Web sites explaining the impact of the
specification changes on the measure result. The MAP's conditions also
specify that CMS continue analyzing the proposed measure to investigate
unexpected results reported in public comment. We stated in the
proposed rule that we intend to fulfill these conditions by offering
additional training opportunities and educational materials in advance
of public reporting, and by continuing to monitor and analyze the
proposed measure. We currently provide private provider feedback
reports as well as a Quarterly Quality Measure report that allows HHAs
to track their measure outcomes for quality improvement purposes. Aside
from those reports, we conduct internal monitoring and evaluation of
our measures to ensure that the measures are performing as they were
intended to perform during the development of the measure. More
information about the MAP's recommendations for this measure is
available at https://www.qualityforum.org/WorkArea/linkit.aspx?LinkIdentifier=id&ItemID=84452.
We reviewed the NQF's consensus endorsed measures and were unable
to identify any home health measures that address changes in skin
integrity related to pressure ulcers. Therefore, based on the evidence
previously discussed, we proposed to adopt the quality measure
entitled, Changes in Skin Integrity Post-Acute Care: Pressure Ulcer/
Injury, for the HH QRP beginning with the CY 2020 HH QRP. We noted that
we plan to submit the proposed measure to the NQF for endorsement
consideration as soon as feasible.
d. Data Collection
The data for this quality measure will be collected using the OASIS
data set, which is currently submitted by HHAs through the Quality
Improvement and Evaluation System (QIES) Assessment Submission and
Processing (ASAP) System. While the inclusion of unstageable wounds in
the proposed measure results in a measure calculation methodology that
is different from the methodology used to calculate the current
pressure ulcer measure, the data elements needed to calculate the
proposed measure are already included on the OASIS data set. In
addition, our proposal to eliminate duplicative data elements that were
used in calculation of the current pressure ulcer measure will result
in an overall reduced reporting burden for HHAs for the proposed
measure. For more information on OASIS data set submission using the
QIES ASAP System, we refer readers to https://www.qtso.com/.
For technical information about this proposed measure, including
information about the measure calculation and the standardized patient
assessment data elements used to calculate this measure, we refer
readers to the document titled Finalized Specifications for HH QRP
Quality Measures and Standardized Patient Assessment Data Elements,
available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html.
We proposed that HHAs will begin reporting the proposed pressure
ulcer measure, Changes in Skin Integrity Post-Acute Care: Pressure
Ulcer/Injury, which will replace the current pressure ulcer measure,
with data collection beginning with respect to admissions and
discharges occurring on or after January 1, 2019.
We solicited public comment on our proposal to remove the current
pressure ulcer measure, Percent of Residents or Patients with Pressure
Ulcers That Are New or Worsened (Short Stay) (NQF #0678), and replace
it with a modified version of that measure, entitled, Changes in Skin
Integrity Post-Acute Care: Pressure Ulcer/Injury, beginning with the CY
2020 HH QRP.
Comment: Several commenters supported the proposed replacement of
the current pressure ulcer measure, Percent of Residents or Patients
with Pressure Ulcers That Are New or Worsened (Short Stay) (NQF #0678),
with a modified version of that measure entitled, Changes in Skin
Integrity Post-Acute Care: Pressure Ulcer/Injury. One of these
commenters noted that this measure will increase the number of
identified pressure ulcers.
One commenter supported the proposed measure calculation approach
because it does not include pressure ulcers that were present at the
time of admission, and noted that a pressure ulcer that is present on
admission is only included in the measure if it subsequently worsens
during the home health episode of care.
Response: We appreciate the commenters' support.
Comment: A few commenters suggested that we make additional
refinements to the proposed measure before we adopt it for the HH QRP;
however, these commenters did not specifically describe any proposed
refinements. One commenter stated generally that the measure was not
fully developed. Another commenter expressed concerns about the
differences between the specifications for this measure in the SNF
setting related to other PAC settings, including the home health
setting. A few commenters additionally commented on the reliability and
validity of the proposed measure, Changes in Skin Integrity Post-Acute
Care: Pressure Ulcer/Injury. Some commenters requested that additional
testing analyses be conducted prior to the implementation of this
measure, and others recommended that we conduct additional testing to
determine the applicability of this measure for its use in the home
health setting. One commenter encouraged CMS to continue to test the
measure to ensure it collects accurate data.
Response: We believe that the Changes in Skin Integrity Post-Acute
Care: Pressure Ulcer/Injury measure is a fully developed measure that
is standardized across the PAC settings, including in the SNF setting.
Testing results for this measure indicated increased observed pressure
ulcer scores in the LTCH, IRF, SNF and HH patient populations when the
unstageable ulcers were included, compared with the previously
implemented pressure ulcer measure. Specifically, an analysis conducted
by the measure development contractor, using data from October through
December 2016, showed mean scores increasing by 2.03 percentage points
in home health, with the addition of unstageable pressure ulcers in the
measure. The changes in the proposed measure also increased the
variability of measures scores.
Further, the reliability and validity of the M0300/M1311 data
elements used to calculate this quality measure have been tested in
several ways. The MDS 3.0 pilot test showed good reliability in the SNF
setting, and we believe that the results are applicable to other post-
acute care providers, including HHAs, because the data elements are
[[Page 51721]]
standardized across the LTCH, IRF, SNF, and HH settings. Testing
conducted to evaluate our ability to derive the measure's numerator
from the M0300 data elements revealed that accuracy improved. The M0300
data elements are standardized with the M1311 data elements used in
OASIS, and we are able to determine that we can also reliably use M1311
data elements to calculate the measure. Additionally, with regard to
the reliability of the pressure ulcer data elements, the average gold-
standard to gold-standard kappa statistic was 0.905. The average gold-
standard to facility-nurse kappa statistic was 0.937. These kappa
scores indicate ``almost perfect'' agreement using the Landis and Koch
standard for strength of agreement.\40\
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\40\ Landis, R., & Koch, G. (1977, March). The measurement of
observer agreement for categorical data. Biometrics 33(1), 159-174.
Landis, R., & Koch, G. (1977, March). The measurement of observer
agreement for categorical data. Biometrics 33(1), 159-174.
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A main difference between the current and proposed pressure ulcer
measures is that the proposed measure includes unstageable pressure
ulcers, including DTIs, in the numerator of the quality measure,
resulting in increased scores in all settings. By including pressure
ulcers that were not included in the numerator of the current pressure
ulcer measure, the scores on the proposed measure are higher and the
risk of the measure being ``topped-out'' is lower.
To assess the construct validity of this measure, or the degree to
which the measure assesses what it claims or purports to be assessing,
our measure contractor sought input from TEPs over the course of
several years. Most recently, on July 18, 2016, a TEP supported the
inclusion in the numerator of unstageable pressure ulcers due to slough
and/or eschar that are new or worsened, new unstageable pressure
ulcers/injuries due to a non-removable dressing or device, and new
DTIs. The measure testing activities were presented to TEP members for
their input on the reliability, validity, and feasibility of the
proposed measure and the changes. The TEP members supported the measure
construct.
We intend to continue to perform reliability and validity testing
to ensure that that the measure demonstrates scientific acceptability
(including reliability and validity) and meets the goals of the HH QRP.
Further, while we intend to validate the data collected to ensure data
accuracy, we note that providers are expected to submit accurate data.
Finally, as with all measure development and implementation, we will
provide training and guidance prior to implementation of the measure to
promote consistency in the interpretation of the measure.
Comment: A few commenters suggested that we monitor the measure for
unintended consequences such as surveillance bias, suggesting that this
could affect measure performance.
Response: We appreciate the comments pertaining to unintended
consequences, including potential bias in reporting the number and
stage of pressure ulcers, which could affect measure performance. We
intend to monitor measure results and item-level responses on an
ongoing basis to identify potential biases or other issues.
Comment: Some commenters expressed concerns pertaining to the
importance of appropriate documentation of unstageable pressure ulcers,
including deep tissue injuries (DTIs). One commenter commented that the
definition of pressure ulcers included in the measure may be too
subjective to collect reliable, accurate measure data across post-acute
care providers, citing DTIs specifically. This commenter added that, as
a result, the measure could provide misleading portrayals of HH
performance.
Response: We appreciate the comments pertaining to the concerns
related to appropriate documentation and definition of unstageable
pressure ulcers. We interpret the commenters' comment regarding
appropriate documentation of unstageable pressure ulcers in the medical
record to mean that as a result of this measure, providers should
ensure such documentation is incorporated into the medical record. We
note that accurate assessment and documentation of all patient
assessment findings is customary for ensuring quality care.
We agree that unstageable pressure ulcers should be appropriately
documented, but disagree that the definition of pressure ulcers used in
the measure may be too subjective to allow for accurate and reliable
data capture in post-acute care settings. The definitions of the
pressure-related ulcers and injuries used in this measure are
standardized and, while all healthcare assessment information can
invoke clinical subjectivity, we believe that the definitions provided
in our guidance manuals, which align with nationally recognized
definitions, enables the collection of data in a reliable manner. We
are also confident, based on the reliability testing results previously
explained, that the measure can accurately assess HHA performance.
Further, we intend to provide training to HHAs to ensure that they
understand how to properly report it.
Comment: Some commenters requested training, help desk support, and
guidance in completing the items that will be used to calculate the
proposed measure. One commenter also recommended that CMS conduct
training on steps HHAs can take to improve quality.
Response: We are currently engaged in efforts to provide
educational activities related to the HH QRP, including training events
and responses to questions submitted to the Help Desk, which will
include information to help HHAs understand how to complete and code
the pressure ulcer. Such educational and training information is part
of our ongoing strategy to ensure successful implementation of the HH
QRP, and ultimately quality improvement. Recordings of previous
trainings are available on the CMS YouTube Web site at https://www.youtube.com/user/CMSHHSgov/featured, and we will continue to make
recordings of trainings available there. We invite HHAs to submit
specific inquiries related to the coding of the OASIS through our help
desk, HHQualityQuestions@cms.hhs.gov. Additionally, a Frequently Asked
Questions document is provided quarterly for the HH QRP, in the
Downloads section of the HH Quality Reporting FAQs Web site at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HH-Quality-Reporting/HH-Quality-Reporting-FAQs-.html. These
FAQ documents are updated to reflect current guidance related to the HH
QRP, including data submission deadlines and training materials.
Comment: One commenter noted the proposed measure requires HHAs to
count the number of unhealed pressure ulcers at each stage and subtract
the number present upon admission. While the commenter agreed that
excluding pressure ulcers that are present on admission is an
appropriate improvement to the measure, the commenter cautioned that it
adds complexity to the coding process. Other commenters stated that
this information may be difficult for providers to capture because of
the new data elements used to calculate the new measure.
Response: We disagree that the proposed measure will require HHAs
to make adjustments to their coding processes because HHAs already
submit the data to calculate the modified measure. Additionally, the
assessment does not require HHAs to tally or count the number of
unhealed pressure ulcers. We perform that calculation for
[[Page 51722]]
purposes of calculating the measure rates.
Comment: Several commenters recommended that CMS attain NQF
endorsement of the Changes in Skin Integrity Post-Acute Care: Pressure
Ulcer/Injury measure prior to implementation.
Response: While this measure is not currently -endorsed by a
consensus-based entity, which is currently the National Quality Forum
(NQF), we believe that this measure possess the attributes necessary
for such endorsement, including the measure's applicability, face
validity and feasibility, and its reliability and validity as derived
from the national testing. Therefore, we believe that this measure is
appropriate for adoption into the HH QRP. However, we intend to submit
this measure to NQF for consideration for its consideration for
endorsement as soon as feasible.
Comment: A few commenters provided feedback on the use of the term
``pressure injury''. Commenters encouraged CMS to use the terminology
recommended by NPUAP and to align with their staging definitions, which
will assist providers to be more standardized.
Response: We have integrated the current language of NPUAP
terminology for coding the patient and resident assessment instruments,
especially in light of the recent updates made by the NPUAP to their
Pressure Ulcer Staging System. The NPUAP announced a change in
terminology to use the term ``pressure injury'' in April 2016.\41\ A
TEP held by our measure development contractor on July 15, 2016, was
supportive of using the term ``pressure injury.'' Some members of the
TEP stated that the term ``injury'' is not associated with blame or
harm by an entity, that ``injury'' may be a more inclusive term than
``ulcer'', and that the term ``pressure injury'' may be more easily and
positively understood by patients, residents, and family members than
``pressure ulcer.'' The TEP recommended training for providers and
consumers regarding any change in terminology. This change will be
accompanied by additional training and guidance for providers,
patients, or residents to clarify any confusion.
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\41\ National Pressure Ulcer Advisory Panel (NPUAP) announces a
change in terminology from pressure ulcer to pressure injury and
updates the stages of pressure injury The National
Pressure Ulcer Advisory Panel--NPUAP. (2016, April 13), from https://www.npuap.org/national-pressure-ulcer-advisory-panel-npuap-announces-a-change-in-terminology-from-pressure-ulcer-to-pressure-injury-and-updates-the-stages-of-pressure-injury/.
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Comment: One commenter suggested that the burden of replacing the
current measure with the modified pressure ulcer measure will be
greater than the burden associated with reporting the current pressure
ulcer measure. The commenter encouraged CMS to streamline reporting and
reduce duplicative efforts. The commenter further commented that CMS
should review the total number of data points, including the OASIS
measure set, to eliminate HHA documentation and administrative burden.
Response: We appreciate the commenter's feedback. We do not believe
that the reporting of the proposed measure will impose a new burden on
HHAs because the measure is calculated using data elements that are
currently included in OASIS that HHAs already submit. As we continue to
refine and modify the OASIS, we will continue to evaluate and avoid any
unnecessary burden associated with the implementation of the HH QRP.
Final Decision: After consideration of the comments received, we
are finalizing our proposal to replace the current pressure ulcer
measure, Percent of Residents or Patients with Pressure Ulcers That Are
New or Worsened (Short Stay) (NQF #0678), with a modified version of
that measure entitled, Changes in Skin Integrity Post- Acute Care:
Pressure Ulcer/Injury, effective with the CY 2020 HH QRP.
2. Addressing the IMPACT Act Domain of Functional Status, Cognitive
Function, and Changes in Function and Cognitive Function: Application
of Percent of Long-Term Care Hospital Patients With an Admission and
Discharge Functional Assessment and a Care Plan That Addresses Function
(NQF #2631)
a. Measure Background
Sections 1899B(c)(1)(A) of the Act requires that no later than the
specified application date (which under section 1899B(a)(1)(E)(ii) is
January 1, 2019 for HHAs, and October 1, 2016 for SNFs, IRFs and
LTCHs), the Secretary specify a quality measure to address the domain
of ``Functional status, cognitive function, and changes in function and
cognitive function.'' We proposed to adopt the measure, Application of
Percent of Long-Term Care Hospital Patients with an Admission and
Discharge Functional Assessment and a Care Plan That Addresses Function
(NQF #2631) for the HH QRP, beginning with the CY 2020 program year.
This is a process measure that reports the percentage of patients with
an admission and discharge functional assessment and treatment goal
that addresses function. The treatment goal provides evidence that a
care plan with a goal has been established for the HH patient.
The National Committee on Vital and Health Statistics' Subcommittee
on Health,\42\ noted that ``information on functional status is
becoming increasingly essential for fostering healthy people and a
healthy population. Achieving optimal health and well-being for
Americans requires an understanding across the life span of the effects
of people's health conditions on their ability to do basic activities
and participate in life situations in other words, their functional
status.'' This is supported by research showing that patient and
resident functioning is associated with important outcomes such as
discharge destination and length of stay in inpatient settings,\43\ as
well as the risk of nursing home placement and hospitalization of older
adults living in the community.\44\ For example, many patients who
utilize HH services may be at risk for a decline in function due to
limited mobility and ambulation.\45\ Thus, impairment in function
activities such as self-care and mobility is highly prevalent in HH
patients. For example, in 98 percent of the over six million HH
episodes in 2015, the patient had at least one limitation or was not
completely independent in self-care activities such as grooming, upper
and lower body dressing, bathing, toilet hygiene, and/or feeding/
eating.\46\
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\42\ Subcommittee on Health National Committee on Vital and
Health Statistics, ``Classifying and Reporting Functional Status''
(2001).
\43\ Reistetter TA, Graham JE, Granger CV, Deutsch A,
Ottenbacher KJ. Utility of Functional Status for Classifying
Community Versus Institutional Discharges after Inpatient
Rehabilitation for Stroke. Archives of Physical Medicine and
Rehabilitation, 2010; 91:345-350.
\44\ Miller EA, Weissert WG. Predicting Elderly People's Risk
for Nursing Home Placement, Hospitalization, Functional Impairment,
and Mortality: A Synthesis. Medical Care Research and Review, 57; 3:
259-297.
\45\ Kortebein, P., Ferrando, A., Lombebeida, J., Wolfe, R., &
Evans, W.J. (2007). Effect of 10 days of bed rest on skeletal muscle
in health adults. JAMA; 297(16):1772-4.
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The primary goal of home health care is to provide restorative care
when improvement is expected, maintain function and health status if
improvement is not expected, slow the rate of functional decline to
avoid institutionalization in an acute or post-acute setting, and/or
facilitate transition to end-of-life care as appropriate.\47\ \48\
[[Page 51723]]
Home health care can positively impact functional outcomes. In stroke
patients, home-based rehabilitation programs administered by home
health clinicians significantly improved ADL function and gait
performance.\49\ Home health services, delivered by a registered nurse,
positively impacted patient Quality of Life (QOL) and clinical
outcomes, including significant improvement in dressing lower body,
bathing meal preparation, shopping, and housekeeping. For some home
health patients, achieving independence within the living environment
and improved community mobility might be the goal of care. For others,
the goal of care might be to slow the rate of functional decline to
avoid institutionalization.\50\
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\47\ Riggs, J.S. & Madigan, E.A. (2012). Describing variation in
home health care episodes for patients with heart failure. Home
Health Care Management and Practice, 24(3): 146-152.
\48\ Ellenbecker, C.H., Samia, L., Cushman, M.J., & Alster, K
(2008). Patient safety and quality: an evidence-based handbook for
nurses. Rockville (MD): agency for healthcare research and quality
(US); 2008 Apr. Chapter 13.
\49\ Asiri, F.Y., Marchetti, G.F., Ellis, J.L., Otis, L.,
Sparto, P.J., Watzlaf, V., & Whitney, S.L. (2014). Predictors of
functional and gait outcomes for persons poststroke undergoing home-
based rehabilitation. Journal of Stroke and Cerebrovascular
Diseases: The Official Journal of National Stroke Association,
23(7), 1856-1864. https://doi.org/10.1016/j.jstrokecerebrovasdis.2014.02.025.
\50\ Ellenbecker, C.H., Samia, L., Cushman, M.J., & Alster, K
(2008). Patient safety and quality: an evidence-based handbook for
nurses. Rockville (MD): agency for healthcare research and quality
(US); 2008 Apr. Chapter 13.
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Patients' functional status is associated with important patient
outcomes, so measuring and monitoring the patients' extent of engaging
in self-care and mobility is valuable. Functional decline among the
elderly; \51\ and chronic illness comorbidities, such as chronic pain
among the older adult population 52 53 are associated with
decreases in self-sufficiency and patient activation (defined as the
patient's knowledge and confidence in self-managing their health).
Impaired mobility, frailty, and low physical activity are associated
with institutionalization,\54\ higher risk of falls and falls-related
hip fracture and death,55 56 greater risk of under
nutrition,\57\ higher rates of inpatient admission from the emergency
department,\58\ and higher prevalence of hypertension and diabetes.\59\
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\51\ Gleason, K.T., Tanner, E.K., Boyd, C. M., Saczynski, J.S.,
& Szanton, S. L. (2016). Factors associated with patient activation
in an older adult population with functional difficulties. Patient
Education and Counseling, 99(8), 1421-1426. https://doi.org/10.1016/j.pec.2016.03.011.
\52\ Roberts AR, Betts Adams K, Beckette & Warner C. (2016).
Effects of chronic illness on daily life and barriers to self-care
for older women: a mixed-methods exploration. J Women Aging, Jul
25:1-11.
\53\ Wu, J.-R., Lennie, T.A., & Moser, D.K. (2016). A
prospective, observational study to explore health disparities in
patients with heart failure-ethnicity and financial status. European
Journal of Cardiovascular Nursing: Journal of the Working Group on
Cardiovascular Nursing of the European Society of Cardiology.
https://doi.org/10.1177/1474515116641296.
\54\ Hajek, A., Brettschneider, C., Lange, C., Posselt, T.,
Wiese, B., Steinmann, S., Weyerer, S., Werle, J., Pentzek, M.,
Fuchs, A., Stein, J., Luck, T., Bickel, H., M[ouml]sch, E., Wagner,
M., Jessen, F., Maier, W., Scherer, M., Riedel-Heller, S.G.,
K[ouml]nig, H.H., & AgeCoDe Study Group. (2015). Longitudinal
Predictors of Institutionalization in Old Age. PLoS One,
10(12):e0144203.
\55\ Akahane, M., Maeyashiki, A., Yoshihara, S., Tanaka, Y., &
Imamura, T. (2016). Relationship between difficulties in daily
activities and falling: loco-check as a self-assessment of fall
risk. Interactive Journal of Medical Research, 5(2), e20. https://doi.org/10.2196/ijmr.5590.
\56\ Zaslavsky, O., Zelber-Sagi, S., Gray, S. L., LaCroix, A.
Z., Brunner, R.L., Wallace, R.B., . . . Woods, N.F. (2016).
Comparison of Frailty Phenotypes for Prediction of Mortality,
Incident Falls, and Hip Fracture in Older Women. Journal of the
American Geriatrics Society, 64(9), 1858-1862. https://doi.org/10.1111/jgs.14233.
\57\ 57 van der Pols-Vijlbrief, R., Wijnhoven, H.A. H., Bosmans,
J.E., Twisk, J.W.R., & Visser, M. (2016). Targeting the underlying
causes of undernutrition. Cost-effectiveness of a multifactorial
personalized intervention in community-dwelling older adults: A
randomized controlled trial. Clinical Nutrition (Edinburgh,
Scotland). https://doi.org/10.1016/j.clnu.2016.09.030.
\58\ Hominick, K., McLeod, V., & Rockwood, K. (2016).
Characteristics of older adults admitted to hospital versus those
discharged home, in emergency department patients referred to
internal medicine. Canadian Geriatrics Journal 202F;: CGJ, 19(1), 9-
14. https://doi.org/10.5770/cgj.19.195.
\59\ Halaweh, H., Willen, C., Grimby-Ekman, A., & Svantesson, U.
(2015). Physical activity and health-related quality of life among
community dwelling elderly. J Clin Med Res, 7(11), 845-52.
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In addition, the assessment of functional ability and provision of
treatment plans directed toward improving or maintaining functional
ability could impact health care costs. Providing comprehensive home
health care, which includes improving or maintaining functional ability
for frail elderly adults, can reduce the likelihood of hospital
readmissions or emergency department visits, leading to reduced health
care service expenditures. 60 61 62 Reducing preventable
rehospitalizations, which made up approximately 17 percent of
Medicare's $102.6 billion in 2004 hospital payments, creates the
potential for large health care cost savings.63 64
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\60\ Hirth, V., Baskins, J., & Dever-Bumba, M. (2009). Program
of all-inclusive care (PACE): Past, present, and future. Journal of
the American Medical Directors Association, 10, 155-160.
\61\ Mukamel, D.B., Fortinsky, R.H., White, A., Harrington, C.,
White, L.M., & Ngo-Metzger, Q. (2014). The policy implications of
the cost structure of home health agencies. Medicare & Medicaid
Research Review, 4(1). https://doi.org/10.5600/mmrr2014-004-01-a03.
\62\ Meunier, M.J., Brant, J.M., Audet, S., Dickerson, D.,
Gransbery, K., & Ciemins, E.L. (2016). Life after PACE (Program of
All-Inclusive Care for the Elderly): A retrospective/prospective,
qualitative analysis of the impact of closing a nurse practitioner
centered PACE site. Journal of the American Association of Nurse
Practitioners. https://doi.org/10.1002/2327-6924.12379.
\63\ Jencks, S.F., Williams, M.V., and Coleman, E.A. (2009).
Rehospitalizations among patients in the Medicare fee-for-service
program. New England Journal of Medicine; 360(14):1418-28.
\64\ Tao, H., Ellenbecker, C.H., Chen, J., Zhan, L., & Dalton,
J. (2012). The influence of social environmental factors on
rehospitalization among patients receiving home health care
services. ANS. Advances in Nursing Science, 35(4), 346-358. https://doi.org/10.1097/ANS.0b013e318271d2ad.
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Further, improving and maintaining functional ability in
individuals with high needs, defined as those with three or more
chronic conditions, may also account for an increase in healthcare
savings. Adults with three or more chronic conditions have nearly four
times the average annual per-person spending for health care services
and prescription medications than the average for all U.S. adults, and
high needs adults with limitations in their ability to perform ADLs,
have even higher average annual health care expenditures.\65\ High
needs individuals with functional limitations spend, on average,
$21,021 on annual health care services, whereas the average annual
health care expenditures for all U.S. adults are approximately
$4,845.45.
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\65\ Hayes, S.L., Salzberg, C.A., McCarthy, D., Radley, DC,
Abrams, M.K., Shah, T., and Anderson, G.F. (2016). High-Need, High-
Cost Patients: Who are they and how do they use health care--A
population-based comparison of demographics, health care use, and
expenditures. The Commonwealth Fund.
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b. Measure Importance
The majority of individuals who receive PAC services, including
care provided by HHAs, SNFs, IRFs, and LTCHs, have functional
limitations, and many of these individuals are at risk for further
decline in function due to limited mobility and ambulation.\66\ The
patient populations treated by HHAs, SNFs, IRFs, and LTCHs vary in
terms of their functional abilities. For example, for home health
patients, achieving independence within the home environment and
promoting community mobility may be the goal of care. For other home
health patients, the goal of care may be to slow the rate of functional
decline in order to allow the person to remain at home and avoid
institutionalization.\67\ The clinical practice guideline Assessment of
Physical Function \68\ recommends that clinicians document functional
status at baseline and over time to validate capacity, decline, or
progress. Therefore, assessment of functional status at admission and
discharge, as well as establishing a functional goal for discharge as
part of the care plan is an
[[Page 51724]]
important aspect of patient or resident care across PAC settings.
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\66\ Kortebein P, Ferrando A, Lombebeida J, Wolfe R, Evans WJ.
Effect of 10 days of bed rest on skeletal muscle in health adults.
JAMA; 297(16):1772-4.
\67\ Ellenbecker CH, Samia L, Cushman MJ, Alster K. Patient
safety and quality in home health care. Patient Safety and Quality:
An Evidence-Based Handbook for Nurses. Vol 1.
\68\ Kresevic DM. Assessment of physical function. In: Boltz M,
Capezuti E, Fulmer T, Zwicker D, editor(s). Evidence-based geriatric
nursing protocols for best practice. 4th ed. New York (NY): Springer
Publishing Company; 2012. p. 89-103.
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Currently, functional assessment data are collected by all four PAC
providers, yet data collection has employed different assessment
instruments, scales, and item definitions. The data cover similar
topics, but are not standardized across PAC settings. The different
sets of functional assessment items coupled with different rating
scales makes communication about patient and resident functioning
challenging when patients and residents transition from one type of
setting to another. Collection of standardized functional assessment
data across HHAs, SNFs, IRFs, and LTCHs using common data items will
establish a common language for patient and resident functioning, which
may facilitate communication and care coordination as patients and
residents transition from one type of provider to another. The
collection of standardized functional status data may also help improve
patient functioning during an episode of care by ensuring that basic
daily activities are assessed for all PAC residents at the start and
end of care, and that at least one functional goal is established.
The functional assessment items included in the proposed functional
status quality measure were originally developed and tested as part of
the Post-Acute Care Payment Reform Demonstration version of the
Continuity Assessment Record and Evaluation (CARE) Item Set, which was
designed to standardize the assessment of a person's status, including
functional status, across acute and post-acute settings (HHAs, SNFs,
IRFs, and LTCHs). The functional status items in the CARE Item Set are
daily activities that clinicians typically assess at the time of
admission and/or discharge to determine patient or resident needs,
evaluate patient or resident progress, and prepare patients, residents,
and their families for a transition to home or to another setting.
The development of the CARE Item Set and a description and
rationale for each item is described in a report entitled ``The
Development and Testing of the Continuity Assessment Record and
Evaluation (CARE) Item Set: Final Report on the Development of the CARE
Item Set: Volume 1 of 3.'' \69\ Reliability and validity testing were
conducted as part of CMS's Post-Acute Care Payment Reform Demonstration
(PAC-PRD), and we concluded that the functional status items have
acceptable reliability and validity. Testing for the functional
assessment items concluded that the items were able to evaluate all
patients on basic self-care and mobility activities, regardless of
functional level or PAC setting. A description of the testing
methodology and results are available in several reports, including the
report entitled ``The Development and Testing of the Continuity
Assessment Record And Evaluation (CARE) Item Set: Final Report On
Reliability Testing: Volume 2 of 3'' \70\ and the report entitled ``The
Development and Testing of The Continuity Assessment Record And
Evaluation (CARE) Item Set: Final Report on Care Item Set and Current
Assessment Comparisons: Volume 3 of 3.'' \71\ These reports are
available on our Post-Acute Care Quality Initiatives Web page at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/CARE-Item-Set-and-B-CARE.html.
---------------------------------------------------------------------------
\69\ Barbara Gage et al., ``The Development and Testing of the
Continuity Assessment Record and Evaluation (CARE) Item Set: Final
Report on the Development of the CARE Item Set'' (RTI International,
2012).
\70\ Ibid.
\71\ Ibid.
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Additional testing of these functional assessment items was
conducted in a small field test occurring in 2016-2017, capturing data
from 12 HHAs. Preliminary data results yielded moderate to substantial
reliability for the self-care and mobility data items. More information
about testing design and results can be found at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/OASIS-Data-Sets.html.
The functional status quality measure we proposed to adopt
beginning with the CY 2020 HH QRP is a process quality measure that is
an application of the NQF-endorsed quality measure, the Percent of
Long-Term Care Hospital Patients with an Admission and Discharge
Functional Assessment and a Care Plan that Addresses Function (NQF
#2631). This quality measure reports the percent of patients with both
an admission and a discharge functional assessment and a functional
treatment goal.
This process measure requires the collection of admission and
discharge functional status data by clinicians using standardized
patient assessment data elements, which assess specific functional
activities, such as self-care and mobility activities. The self-care
and mobility function activities are coded using a 6-level rating scale
that indicates the patient's level of independence with the activity at
both admission and discharge. A higher score indicates more
independence. These functional assessment data elements will be
collected at Start or Resumption of Care (SOC/ROC) and discharge.
For this quality measure, there must be documentation at the time
of admission (SOC) that at least one activity performance (function)
goal is recorded for at least one of the standardized self-care or
mobility function items using the 6-level rating scale. This indicates
that an activity goal(s) has been established. Following this initial
assessment, the clinical best practice will be to ensure that the
patient's care plan reflected and included a plan to achieve such
activity goal(s). At the time of discharge, goal setting and
establishment of a care plan to achieve the goal, is reassessed using
the same 6-level rating scale, allowing for the ability to evaluate
success in achieving the patient's activity performance goals.
To the extent that a patient has an unplanned discharge, for
example, transfer to an acute care facility, the collection of
discharge functional status data may not be feasible. Therefore, for
patients with unplanned discharges, admission functional status data
and at least one treatment goal must be reported, but discharge
functional status data are not required to be reported.
c. Stakeholder Feedback
Our measures contractor convened a TEP on October 17 and October
18, 2016. The TEP was composed of a diverse group of stakeholders with
HH, PAC, and functional assessment expertise. The panel provided input
on the technical specifications of this proposed measure, including the
feasibility of implementing the measure, as well as the overall measure
of reliability and validity. The TEP additionally provided feedback on
the clinical assessment items used to calculate the measure. The TEP
reviewed the measure ``Percent of Long-Term Care Patients with an
Admission and Discharge Functional Assessment and a Care Plan That
Addresses Function (NQF 2631)'' for potential application to the home
health setting. Overall they were supportive of a functional process
measure, noting it could have the positive effect of focusing clinician
attention on functional status and goals. A summary of the TEP
proceedings is available on the PAC Quality Initiatives Downloads and
Videos Web page at https://www.cms.gov/medicare/quality-initiatives-
patient-assessment-instruments/post-acute-care-quality-initiatives/
impact-act-of-2014/impact-act-downloads-and-videos.html.
[[Page 51725]]
We also solicited stakeholder feedback on the development of this
measure through a public comment period held from November 4, 2016
through December 5, 2016. Several stakeholders and organizations
supported this measure for implementation and for measure
standardization. Some commenters also provided feedback on the
standardized patient assessment data elements used to calculate the
proposed quality measure. Commenters offered suggestions, including
providing education regarding the difference in measure scales for the
standardized items relative to current OASIS functional items, and
guidance on the type of clinical staff input needed to appropriately
complete new functional assessment items. Commenters also addressed the
feasibility of collecting data for the individual standardized self-
care and mobility items in the home health setting. Finally, commenters
noted the importance of appropriate goal setting when functional
improvement for a patient may not be feasible. The public comment
summary report for the proposed measure is available on the CMS Web
site at https://www.cms.gov/medicare/quality-initiatives-patient-
assessment-instruments/post-acute-care-quality-initiatives/impact-act-
of-2014/impact-act-downloads-and-videos.html.
The NQF-convened MAP met on December 14 and 15, 2016, and provided
input on the use of this proposed measure in the HH QRP. The MAP
recommended ``conditional support for rulemaking'' for this measure.
MAP members noted the measure will drive care coordination and improve
transitions by encouraging the use of standardized functional
assessment items across PAC settings, but recommended submission to the
NQF for endorsement to include the home health setting. More
information about the MAP's recommendations for this measure is
available at https://www.qualityforum.org/Publications/2017/02/MAP_2017_Considerations_for_Implementing_Measures_in_Federal_Programs_-_PAC-LTC.aspx.
We reviewed the NQF's consensus endorsed measures and were unable
to identify any home health measures that address functional assessment
and treatment goals that that address function. However, we were able
to identify five functional measures in home health that assess
functional activities only, without a treatment goal. These measures
are: (1) Improvement in Ambulation/Locomotion (NQF #0167); (2)
Improvement in Bathing (NQF #0174); (3) Improvement in Bed Transfer
(NQF #0175); (4) Improvement in Management of Oral Medications (NQF #
0176); and (5) Improvement in Pain Interfering with Activity (NQF
#0177). Our review determined that these setting-specific measures are
not appropriate to meet the specified IMPACT Act domain as they do not
include standardized items or are not included for various other PAC
populations. Specifically--
The items used to collect data for the current home health
measures are less specific, leading to broader measure results, whereas
the standardized patient assessment data items used for the proposed
measure assess core activities such as rolling in bed, walking a
specified distance, or wheelchair capability.
The item coding responses are more detailed when compared
to the non-standardized OASIS item responses, allowing for more
granular data for the measure.
The proposed functional measure will capture a patient's
discharge goal at admission into home health; this detail is not
captured in the existing endorsed HH function measures.
Therefore, based on the evidence discussed previously, we proposed
to adopt the quality measure entitled, Application of Percent of Long-
Term Care Hospital Patients with an Admission and Discharge Functional
Assessment and a Care Plan That Addresses Function (NQF #2631), for the
HH QRP beginning with the CY 2020 HH QRP. We noted that we plan to
submit the proposed measure to the NQF for endorsement consideration as
soon as is feasible.
For technical information about the proposed measure, including
information about the measure calculation and the standardized patient
assessment data elements used to calculate this measure, we referred
readers to the document titled, Final Specifications for HH QRP Quality
Measures and Standardized Patient Assessment Data, available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html.
d. Data Collection
For purposes of assessment data collection, we proposed to add new
functional status items to the OASIS, to be collected at SOC/ROC and
discharge. These items will assess specific self-care and mobility
activities, and will be based on functional items included in the PAC-
PRD version of the CARE Item Set. More information pertaining to item
testing is available on our Post-Acute Care Quality Initiatives Web
page at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/CARE-Item-Set-and-B-CARE.html.
To allow HHAs to fulfill the requirements of the Home Health Agency
Conditions of Participation (HHA CoPs) (82 FR 4509), we proposed to add
a subset of the functional assessment items to the OASIS, with
collection of these items at Follow-Up (FU). The collection of these
assessment items at FU by HHAs will allow them to fulfill the
requirements outlined in the HHA CoPs that suggest that the collection
of a patient's current health, including functional status, be
collected on the comprehensive assessment.
This new subset of functional status items are standardized across
PAC settings and support the proposed standardized measure. They are
organized into two functional domains: Self-Care and Mobility. Each
domain includes dimensions of these functional constructs that are
relevant for home health patients. The proposed function items that we
proposed to add to the OASIS for purposes of the calculation of this
proposed quality measure would not duplicate existing items currently
collected in that assessment instrument for other purposes. The current
OASIS function items evaluate current ability, whereas the proposed
functional items would evaluate an individual's usual performance at
the time of admission and at the time of discharge for goal setting
purposes. Additionally, we noted that there are several key differences
between the existing and new proposed function items that may result in
variation in the patient assessment results including: (1) The data
collection and associated data collection instructions; (2) the rating
scales used to score a resident's level of independence; and (3) the
item definitions. A description of these differences is provided with
the measure specifications available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html.
Because of the differences between the current function assessment
items (OASIS C-2) and the proposed function assessment items that we
would collect for purposes of calculating the proposed measure, we
would require that HHAs submit data on both sets of items. Data
collection for the new proposed function items do not substitute for
the data collection under the current OASIS ADL and IADL items, and as
discussed previously, we do not believe that the
[[Page 51726]]
items are duplicative. However, we solicited comment on opportunities
to streamline reporting to avoid duplication and minimize burden.
We proposed that data for the proposed quality measure would be
collected through the OASIS, which HHAs currently submit through the
QIES ASAP system. We referred readers to section V.F.2 of the proposed
rule (82 FR 35345 through 35353) for more information on the proposed
data collection and submission timeline for this proposed quality
measure. We noted that if this measure is finalized, we intended to
provide initial confidential feedback to home health agencies, prior to
the public reporting of this measure.
We solicited public comment on our proposal to adopt the measure,
Application of Percent of Long-Term Care Hospital Patients with an
Admission and Discharge Functional Assessment and a Care Plan That
Addresses Function (NQF #2631).
Comment: A number of commenters supported the proposed measure,
Application of Percent of Long-Term Care Hospital Patients with an
Admission and Discharge Functional Assessment and a Care Plan That
Addresses Function (NQF #2631). MedPAC acknowledged the value of a
functional status quality measure that would be standardized with other
functional status quality measures across the four PAC settings.
Response: We appreciate the commenters' support of the measure.
Comment: Some commenters suggested that CMS refine the measure and
conduct additional testing for home health setting applicability before
adopting it Other commenters recommended that we provide training and
give HHAs time to adjust their workflow to both accommodate the new
measure and the removal of duplicative data elements in the OASIS.
Further, a few commenters expressed concern over the addition of the
items used to calculate the proposed process quality measure, claiming
that the items will be duplicative and that the legacy items must be
removed from the OASIS-C2 assessment instrument to limit provider
burden. Commenters also requested that CMS consider the additional
resources providers will need to accommodate item set changes and
encouraged ongoing education efforts for new data elements.
Response: The items for this measure were rigorously tested in the
Post-Acute Care Payment Reform Demonstration (PAC PRD). Based on
testing from the PAC PRD, the inter-rater reliability of the items
needed to calculate this measure was favorable, with items' kappa
scores between 0.59 and 0.80. This is important for measuring progress
in some of the most complex cases treated in post-acute care settings.
The data elements developed to calculate this proposed process measure
were also tested in a comprehensive field test of existing and
potential OASIS data elements and found to be feasible with acceptable
levels of inter-rater reliability, as described at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/OASIS-Data-Sets.html.
Although HHAs will need to incorporate the data on this measure
into their workflow, we do not believe that these data elements are
duplicative of other data already collected. The items needed to
calculate the proposed measure different assessment scales, coding
options for those with medical complexities, and have different
definitions for items and activities, and the proposed measure's data
elements evaluate usual performance in various manners. Further, to
reduce potential burden associated with collecting the proposed
measure, we have included several mechanisms to reduce the number of
items that apply to any one patient. For example, there are gateway
questions pertaining to walking and wheelchair mobility that allow the
clinician to skip items that ask if the patient does not walk or does
not use a wheelchair, respectively.
Comment: Commenters provided feedback on the reliability and
validity of the items necessary to calculate the function process
measure. Some of these commenters expressed concern that the proposed
function measure has not undergone testing and validation in the home
health setting or may not be applicable for home health setting as in
the facility-based post-acute care settings. One of these commenter
expressed concern that the scales used to assess the items for the
proposed process quality measure and the current OASIS functional
assessment items are different, which could affect the items'
reliability and validity. Another commenter raised concern with the
difference in timeframe allowed for data collection when compared to
other OASIS items.
Response: In the PAC PRD, the functional activity items (self-care
and mobility) were tested sufficiently in HHAs and with sufficient
patients to support reliability. The functional assessment items were
compared to other functional assessment instrument data (including
OASIS functional assessment items), as part of the PAC-PRD analyses
with positive results. The inter-rater reliability of the functional
activity items has been tested and the results have been favorable with
items' kappa scores between .59 and .80. We also conducted analyses of
the internal consistency of the function data analyses which indicate
moderate to substantial agreement suggesting sufficient reliability for
the items used to calculate the proposed process quality measure.
We acknowledge that the scale for the items used to calculate the
proposed quality measure vary from the scales that are used in current
OASIS-C2 items. The scale used to assess the items for the proposed
process quality measure assesses independence in functional activities
(a higher score indicates greater independence). We believe that the 6-
level scale will allow us to better distinguish change at the highest
and lowest levels of patient functioning by documenting minimal change
from no change at the low end of the scale.\72\ The PAC PRD supported
the use of the scale in HHAs with both the alpha testing and beta
testing reinforcing the clinical logic and consistency of language for
the functional assessment items. The items in section GG were developed
with input from clinicians and stakeholders to better measure the
change in function, regardless of the severity of the individual's
impairment.
---------------------------------------------------------------------------
\72\ Barbara Gage et al., ``The Development and Testing of the
Continuity Assessment Record and Evaluation (CARE) Item Set: Final
Report on the Development of the CARE Item Set'' (RTI International,
2012).
---------------------------------------------------------------------------
The items used to calculate the proposed process quality measure
are standardized across the four PAC settings, based on the need for
data to reflect the patient's status at the time of SOC/ROC and EOC. We
are currently conducting testing across the four PAC settings to align
the most appropriate time frame of data collection at admission/SOC and
at discharge/EOC.
A full description of the analyses and the results are provided in
the report, The Development and Testing of the Continuity Assessment
Record and Evaluation (CARE) Item Set: Final Report on the Development
of the CARE Item Set and Current Assessment Comparisons Volume 3 of 3,
and the report is available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/CARE-Item-Set-and-B-CARE.html. Additional testing of the
Section GG items with the OASIS functional items was recently completed
[[Page 51727]]
and will to continue to help inform guidance for HH providers.
Comment: One commenter suggested that the OASIS should include an
assessment of Instrumental Activities of Daily Living (IADL) as a part
of functional assessment.
Response: We appreciate the commenter's recommendation and will
take it into consideration in future measure refinement work.
Comment: Commenters expressed concern about different clinical
staff assessing functional status and setting functional goals across
PAC settings, noting that in some settings, such as SNFs, licensed
physical therapists typically assess function and set functional goals,
whereas in HHAs, nurses typically perform that assessment. Commenters
noted that setting a goal will pose a challenge for nurses in the home
health setting.
Response: We are unclear why the commenters believe that goal
setting will be more difficult in the home health setting than in other
settings. The goals being assessed through the measure are intended to
be set by patients, not clinicians. In addition, the original testing
of the assessment items used for the proposed measure included a wide
variety of clinicians to assess item collection, coding and
reliability. For more information on testing results, we refer readers
to the PAC PRD final report located at: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/Downloads/The-Development-and-Testing-of-the-Continuity-Assessment-Record-and-Evaluation-CARE-Item-Set-Final-Report-on-the-Development-of-the-CARE-Item-Set-Volume-1-of-3.pdf.
Final Decision: After consideration of the comments received, we
are finalizing, as proposed, the adoption of the measure entitled the
Application of Percent of Long-Term Care Hospital Patients with an
Admission and Discharge Functional Assessment and a Care Plan That
Addresses Function (NQF #2631) for the HH QRP beginning with the CY
2020 program year.
3. Addressing the IMPACT Act Domain of ``Incidence of Major Falls''
Measure: Percent of Residents Experiencing One or More Falls With Major
Injury
a. Measure Background
Section 1899B(c)(1)(D) of the Act requires that no later than the
specified application date (which under section 1899B(a)(1)(E)(i)(IV)
of the Act is January 1, 2019 for HHAs, and October 1, 2016 for SNFs,
IRFs and LTCHs), the Secretary specify a measure to address the domain
of incidence of major falls, including falls with major injury. We
proposed to adopt the measure, Application of Percent of Residents
Experiencing One or More Falls with Major Injury (NQF #0674), for which
we would begin to collect data on January 1, 2019 for the CY 2020 HH
QRP to meet this requirement. This proposed outcome measure reports the
percentage of patients who have experienced falls with major injury
during episodes ending in a 3-month period.
b. Measure Importance
Falls affect an estimated 6 to 12 million older adults each year
and are the leading cause of both fatal injury and nonfatal hospital
admissions.73 74 Within the home health population, the risk
of falling is significant as approximately one third of individuals
over the age of 65 experienced at least one fall annually.\75\ Major
fall-related injuries among older community-dwelling adults are a
growing health concern within the United States 76 77
because they can have high medical and cost implications for the
Medicare community.\78\ In 2013, the direct medical cost for falls in
older adults was $34 billion \79\ and is projected to increase to over
$101 billion by 2030 due to the aging population.\80\
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\73\ Bohl, A.A., Phelan, E.A., Fishman, P.A., & Harris, J R.
(2012). How are the costs of care for medical falls distributed? The
costs of medical falls by component of cost, timing, and injury
severity. The Gerontologist, 52(5): 664-675.
\74\ National Council on Aging (2015). Falls Prevention Fact
Sheet. Retrieved from https://www.ncoa.org/wp-content/;uploads/Fact-
Sheet_Falls-Prevention.pdf.
\75\ Avin G.K., Hanke A.T., Kirk-Sanche, N., McDonough M.C.,
Shubert E.T., Hardage, J.,& Hartley, G. (2015). Management of Falls
in Community-Dwelling Older Adults: Clinical Guidance Statement From
the Academy of Geriatric Physical Therapy of the American Physical
Therapy Association. Physical Therapy, 95(6), 815-834. doi:10.2522/
ptj.20140415.
\76\ Hester, A.L. & Wei, F. (2013). Falls in the community:
State of the science. Clinical Interventions in Aging, 8:675-679.
\77\ Orces, C.H. & Alamgir, H. (2014). Trends in fall-related
injuries among older adults treated in emergency departments in the
USA. Injury Prevention, 20: 421-423.
\78\ Liu, S.W., Obermeyer, Z., Chang, Y., & Shankar, K.N.
(2015). Frequency of ED revisits and death among older adults after
a fall. American Journal of Emergency Medicine, 33(8), 1012-1018.
doi:10.1016/j.ajem.2015.04.023.
\79\ Centers for Disease Control and Prevention (2015b).
Important facts about falls. https://www.cdc.gov/homeandrecreationalsafety/falls/adultfalls.html. Accessed April 19,
2016.
\80\ Houry, D., Florence, C. Bladwin, G., Stevens, J., &
McClure, R. (2015). The CDC Injury Center's response to the growing
public health problem of falls among older adults. American Journal
of Lifestyle Medicine, 10(1), 74-77.
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Evidence from various studies indicates that implementing effective
fall prevention interventions and minimizing the impact of falls that
do occur reduces overall costs, emergency department visits, hospital
readmissions, and overall Medicare resource
utilization.81 82 83 84 In the 2006 Home Assessments and
Modification study, a home visit by an occupational therapist or home
care worker to identify and mitigate potential home hazards and risky
behavior, resulted in a 46 percent reduction in fall rates for those
receiving the intervention
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\81\ Bamgbade, S., & Dearmon, V. (2016). Fall prevention for
older adults receiving home healthcare. Home Healthcare Now, 34(2),
68-75.
\82\ Carande-Kulis, V., Stevens, J.A., Florence, C.S., Beattie,
B.L., & Arias, I. (2015). A cost-benefit analysis of three older
adult fall prevention interventions. Journal of Safety Research, 52,
65-70. doi:10.1016/j.jsr.2014.12.007.
\83\ Cohen, A.M., Miller, J., Shi, X., Sandhu, J., & Lipsitz, A.
(2015). Prevention program lowered the risk of falls and decreased
claims for long-term care services among elder participants. Health
Affairs, 34(6), 971-977.
\84\ Howland, J., Shankar, K.N., Peterson, E.W., & Taylor, A.A.
(2015). Savings in acute care costs if all older adults treated for
fall-related injuries completed matter of balance. Injury
Epidemiology, 2(25), 1-7.
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compared to controls.\85\ Overall, patients participating in
interventions experienced improved quality of life due to reduced
morbidity, improved functional ability and mobility, reduced number of
falls and injurious falls, and a decrease in the fear of falling.\86\
\87\ Falls also represent a significant cost burden to Medicare. Each
year, 2.8 million older people are treated in Emergency Departments for
fall related injuries and over 800,000 require hospitalization.\88\
Adjusted to 2015 dollars, nationally, direct medical costs for nonfatal
fall related injuries in older adults were over $31.3 billion.\89\
Additional health care costs (in 2010 dollars) can range from $3,500
for a fall without serious injury to $27,000 for a
[[Page 51728]]
fall with a serious injury.\90\ Between 1988 and 2005, fractures
accounted for 84 percent of hospitalizations for fall-related injuries
among older adults.\91\ Researchers evaluated the cost of fall-related
hospitalizations among older adults using the 2011 Texas Hospital
Inpatient Discharge Data and determined that the average cost for fall-
related hip fractures was $61,715 for individuals 50 and older living
in metropolitan areas and $55,366 for those living nonmetropolitan
areas.\92\
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\85\ Pighills AC, Torgerson DJ, Sheldon TA, Drummond AE, Bland
JM. Environmental assessment and modification to prevent falls in
older people. Journal of the American Geriatrics Society.
2011;59(1):26-33.
\86\ Chase, C.A., Mann, K., Wasek, S., & Arbesman, M. (2012).
Systematic review of the effect of home modification and fall
prevention programs on falls and the performance of community-
dwelling older adults. American Journal of Occupational Therapy,
66(3), 284-291.
\87\ Patil, R., Uusi-Rasi, K., Tokola, K., Karinkanta, S.,
Kannus, P., & Sievanen, H. (2015). Effects of a Multimodal Exercise
Program on Physical Function, Falls, and Injuries in Older Women: A
2-Year Community-Based, Randomized Controlled Trial. Journal of the
American Geriatrics Society, 63(7), 1306-1313.
\88\ Centers for Disease Control and Prevention, National Center
for Injury Prevention and Control. Web-based Injury Statistics Query
and Reporting System (WISQARS) [online]. Accessed August 5, 2016.
\89\ Burns ER, Stevens JA, Lee R. The direct costs of fatal and
non-fatal falls among older adults--United States. J Safety Res
2016;58:99-103.
\90\ Wu S, Keeler EB, Rubenstein LZ, Maglione MA, Shekelle PG. A
cost-effectiveness analysis of a proposed national falls prevention
program. Clin Geriatr Med. 2010;26(4): 751-66.
\91\ Orces, C.H. & Alamgir, H. (2014). Trends in fall-related
injuries among older adults treated in emergency departments in the
USA. Injury Prevention, 20: 421-423.
\92\ Towne, S.D., Ory, M.G., & Smith, M.L. (2014). Cost of fall-
related hospitalizations among older adults: Environmental
comparisons from the 2011 Texas hospital inpatient discharge data.
Population Health Management, 17(6), 351-356.
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To meet the IMPACT Act provision requiring the development of a
standardized quality measure for the domain of Incidence of Major Falls
(sections 1899B(c)(1)(D) of the Act), we proposed the standardized
measure, The Percent of Residents Experiencing One or More Falls with
Major Injury (Long Stay) (NQF #0674). We noted that this quality
measure is NQF-endorsed and has been successfully implemented in the
Nursing Home Quality Initiative for nursing facility long-stay
residents since 2011, demonstrating the measure is feasible,
appropriate for assessing PAC quality of care, and could be used as a
platform for standardized quality measure development. This quality
measure is standardized across PAC settings and contains items that are
collected uniformly in each setting's assessment instruments (that is,
MDS, IRF-PAI, and LCDS). Further, an application of the quality measure
was adopted for use in the LTCH QRP in the FY 2014 IPPS/LTCH PPS final
rule (78 FR 50874 through 50877), revised in the FY 2015 IPPS/LTCH PPS
final rule (79 FR 50290 through 50291), and adopted to fulfill IMPACT
Act requirements in the FY 2016 IPPS/LTCH PPS final rule (80 FR 49736
through 49739). Data collection began in April 1, 2016 for LTCHs, and
October 1, 2016 for SNFs and IRFs.
More information on the NQF-endorsed quality measure, the Percent
of Residents Experiencing One or More Falls with Major Injury (Long
Stay) (NQF #0674) is available at https://www.qualityforum.org/QPS/0674.
c. Stakeholder Feedback
A TEP convened by our measure development contractor provided input
on the technical specifications of an application of the quality
measure, the Percent of Residents Experiencing One or More Falls with
Major Injury (Long Stay) (NQF #0674), including the feasibility of
implementing the measure across PAC settings. The TEP was supportive of
the implementation of this measure across PAC settings and was also
supportive of our efforts to standardize this measure for cross-setting
development. More information about this TEP can be found at https://
www.cms.gov/medicare/quality-initiatives-patient-assessment-
instruments/post-acute-care-quality-initiatives/impact-act-of-2014/
impact-act-downloads-and-videos.html.
In addition, we solicited public comment on this measure from
September 19, 2016, through October 14, 2016. Overall, commenters were
generally supportive of the measure, but raised concerns about the
attribution given that home health clinicians are not present in the
home at all times and recommended risk-adjusting the measure. The
summary of this public comment period can be found at https://
www.cms.gov/medicare/quality-initiatives-patient-assessment-
instruments/post-acute-care-quality-initiatives/impact-act-of-2014/
impact-act-downloads-and-videos.html.
Finally, we presented this measure to the NQF-convened MAP on
December 14, 2016. The MAP conditionally supported the use of an
application of the quality measure, the Percent of Residents
Experiencing One or More Falls with Major Injury (Long Stay) (NQF
#0674) in the HH QRP as a cross-setting quality measure. The MAP
highlighted the clinical significance of falls with major injury, while
noting potential difficulties in collecting falls data and more limited
action ability in the home health setting. The MAP suggested that CMS
explore stratification of measure rates by referral origin when public
reporting. More information about the MAP's recommendations for this
measure is available at https://www.qualityforum.org/Publications/2017/02/MAP_2017_Considerations_for_Implementing_Measures_in_Federal_Programs_-_PAC-LTC.aspx. We solicited public comment on the stratification of the
proposed measure, specifically on the measure rates for public
reporting. The quality measure, the Percent of Residents Experiencing
One or More Falls with Major Injury (Long Stay) (NQF #0674) is not
currently endorsed for the home health setting. We reviewed the NQF's
consensus endorsed measures and were unable to identify any NQF-
endorsed cross-setting quality measures for that setting that are
focused on falls with major injury. We found one falls-related measure
in home health titled, Multifactor Fall Risk Assessment Conducted for
All Patients Who Can Ambulate (NQF #0537).
We noted that we are also aware of one NQF-endorsed measure, Falls
with Injury (NQF #0202), which is a measure designed for adult acute
inpatient and rehabilitation patients capturing ``all documented
patient falls with an injury level of minor or greater on eligible unit
types in a calendar quarter, reported as injury falls per 100 days.''
\93\ After careful review, we determined that these measures are not
appropriate to meet the IMPACT Act domain of incidence of major falls.
Specifically--
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\93\ American Nurses Association (2014, April 9). Falls with
injury. Retrieved from https://www.qualityforum.org/QPS/0202.
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NQF #0202 includes minor injuries in the numerator
definition. Including all falls in an outcome measure could result in
providers limiting activity for individuals at higher risk for falls.
NQF #0537 is a process-based measure of HHAs' efforts to
assess the risk for any fall, but not actual falls.
Neither measure is standardized across PAC settings.
We are unaware of any other cross-setting quality measures for
falls with major injury that have been endorsed or adopted by another
consensus organization for the Home health setting. Therefore, based on
the evidence discussed previously, we proposed to adopt the quality
measure entitled, An Application of the Measure Percent of Residents
Experiencing One or More Falls with Major Injury (Long Stay) (NQF
#0674), for the HH QRP beginning with the CY 2020 HH QRP. We noted in
the proposed rule that we plan to submit the proposed measure to the
NQF for endorsement consideration as soon as it is feasible.
d. Data Collection
For purposes of assessment data collection, we proposed to add two
new falls-related items to the OASIS. The proposed falls with major
injury item used to calculate the proposed quality measure does not
duplicate existing items currently collected in the OASIS. We proposed
to add two standardized items to the OASIS for collection at EOC, which
comprises the Discharge from Agency, Death at Home, and Transfer to an
Inpatient Facility time
[[Page 51729]]
points: J1800 and J1900. The first item (J1800) is a gateway item that
asks whether the patient has experienced any falls since admission/
resumption of care (prior assessment). If the answer to J1800 is yes,
the next item (J1900) asks for the number of falls with: (a) No injury,
(b) injury (except major), and (c) major injury. The measure is
calculated using data reported for J1900C (number of falls with major
injury). This measure would be calculated at the time of discharge (see
82 FR 35351). For technical information about this proposed measure,
including information pertaining to measure calculation and the
standardized patient assessment data element used to calculate this
measure, we referred readers to the document titled, Final
Specifications for HH QRP Quality Measures and Standardized Patient
Assessment Data, available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html.
We proposed that data for the proposed quality measure would be
collected through the OASIS, which HHAs currently submit through the
QIES ASAP system. We referred readers to section V.I.4 of the proposed
rule for more information on the proposed data collection and
submission timeline for this proposed quality measure.
We solicited public comments on our proposal to adopt an
application of the quality measure, the Percent of Residents
Experiencing One or More Falls with Major Injury (Long Stay) (NQF
#0674) beginning with the CY 2020 HH QRP.
Comment: A few commenters supported the proposed measure,
Application of Percent of Residents Experiencing One or More Falls With
Major Injury (Long Stay) (NQF #0674), noting that it aligned with
measures in other post-acute care settings.
Response: We appreciate the commenters' support of the proposed
measures.
Comment: Several commenters suggested that CMS further refine and
test Application of Percent of Residents Experiencing One or More Falls
With Major Injury (Long Stay) (NQF #0674), to determine HHA setting
applicability before adopting it for the HH QRP. Other commenters
recommended that we provide training and time for HHAs to accommodate
the new measures into their workflow. One commenter recommended that we
review the impact of new measures on high needs beneficiaries.
Response: This measure is fully developed and testing of this
measure is based on a comprehensive field test of the items used to
calculate this measure. Further, feedback from clinicians suggested
that the items used to calculate this measure are feasible to collect
in a Home health setting, reinforcing the measure testing by CMS and
their measure contractor. Therefore, by way of testing results and
consensus vetting, we believe that this measure is applicable to a home
health setting.
With respect to training, we intend to engage in multiple
activities including updating our manual and conducting training
sessions, to ensure that HHAs understand how to properly report the
measure.
Comment: A few commenters addressed the administrative burden of
the measure, specifically focusing on the addition of items used in its
calculation to the OASIS. Specifically, one of these commenters
encouraged CMS to review the overall number of OASIS data elements and
measures. The same commenter noted that HHAs already are evaluated on a
falls measure, ``Multifactor Fall Risk Assessment Conducted for All
Patients Who Can Ambulate''.
Response: This proposed measure is an outcome measure that we are
adopting to satisfy the measure domain, Incidence of Major Falls,
required by the IMPACT Act. The process measure, ``Multifactor Fall
Risk Assessment Conducted for All Patients Who Can Ambulate'', is a
measure that assesses falls risk rather than the outcome of a major
fall. That measure is not aligned across post-acute care settings and
therefore does not meet the requirements of the IMPACT Act.
Pertaining to the administrative burden, the proposed measure,
``Falls with Major Injury,'' requires a total of two items to be added
to the OASIS, which were considered feasible for collection in post-
acute care settings. We believe these items add minimally to the
quality reporting burden.
Comment: Several commenters noted that the home health setting is
unique from facility-based care, making it difficult to assess or
prevent patient falls. Commenters noted that home health staff are not
with their patients around the clock, unlike facility-based care, and
that patients may refuse or decline to follow staff recommendations on
falls prevention.
Response: Assessing the incidence of major falls, which is
associated with morbidity, mortality, and high costs, is required under
the IMPACT Act and is also one of our major priorities for improving
the quality of patient care. In order to ensure that this measure is
appropriate for a home health setting, we examined fall risk and
prevalence among the cohort of home health patients by means of an
analysis using 2015 OASIS data. In nearly 32 percent of the 5.3 million
episodes with relevant data, the patient had a history of falls,
defined as two or more falls, or any fall with an injury, in the
previous 12 months. For the more than 6.1 million episodes where the
patient received a multi-factor falls risk assessment using a
standardized, validated assessment tool, the patient was found to have
falls risk 93 percent of the time. Additionally, there were nearly
100,000 instances documented where a patient required emergency care
for an injury due to a fall. Our environmental scan identified
evidence-based strategies that can and have been applied in the home
health setting to reduce falls risk. Therefore, we believe that a
measure of this type is important for both providers and individuals,
to support person-centered care to properly assess for the risk of
falling accompanied by a major injury to support proper care planning.
In addition to meeting the requirements of the IMPACT Act, this measure
will address the current gap in the HH QRP measure set for this type of
injurious fall.
Comment: Several commenters recommended that this measure be risk-
adjusted for the purpose of public-reporting, and that unadjusted rates
be shared with providers via confidential feedback only. Commenters
additionally suggested that there may be unintended consequences
without risk adjustment such that HHAs may be hesitant to accept higher
falls' risk patients for fear of the financial impact. The commenters
stated that this may potentially limit the value of comparison amongst
HHAs. According to one of these commenters, without risk adjustment,
the measure could present a distorted correlation between the rate of
major injuries related to falls and the quality of care provided by the
agency. This will limit comparisons among home health agencies. Another
commenter noted that stratifying results for public reporting may not
be feasible given sample sizes and will not be a substitute for risk-
adjustment.
Response: While we acknowledge that various patient characteristics
can elevate the risk for falls, falls with major injury are considered
to be `never events. A never event is a serious reportable event. For
that reason, we do not believe we should risk adjust the proposed
measure. Risk adjusting for falls with major injury could
unintentionally lead to insufficient risk prevention by the provider.
The need for risk assessment, based on varying
[[Page 51730]]
risk factors among residents, does not remove the obligation of
providers to minimize that risk.
Comment: Many commenters noted that the falls measure is not
endorsed by NQF for the home health setting and encouraged CMS to
pursue NQF endorsement.
Response: While this measure is not currently NQF-endorsed, we
recognize that the NQF endorsement process is an important part of
measure development and we plan to submit this measure for NQF
endorsement consideration as soon as feasible.
Final Decision: After consideration of the comments received, we
are finalizing as proposed the measure Percent of Residents
Experiencing One or More Falls with Major Injury for adoption in the HH
QRP beginning with the CY 2020 program year.
G. HH QRP Quality Measures and Measure Concepts Under Consideration for
Future Years
We solicited public comment on the importance, relevance,
appropriateness, and applicability of each of the quality measures
listed in Table 19 for use in future years in the HH QRP.
Table 19--HH QRP Quality Measures Under Consideration for Future Years
------------------------------------------------------------------------
Functional status, cognitive function,
IMPACT Act domain and changes in function and cognitive
function
------------------------------------------------------------------------
Measures..................... A. Application of NQF #2633--Change in
Self-Care Score for Medical
Rehabilitation Patients.
B. Application of NQF #2634--Change in
Mobility Score for Medical
Rehabilitation Patients.
C. Application of NQF #2635--Discharge
Self-Care Score for Medical
Rehabilitation Patients.
D. Application of NQF #2636--Discharge
Mobility Score for Medical
Rehabilitation Patients.
------------------------------------------------------------------------
We noted that we are considering four measures that will assess a
change in functional outcomes such as self-care and mobility across a
HH episode. These measures would be standardized to measures finalized
in other PAC quality reporting programs, such as the IRF QRP. We
solicited feedback on the importance, relevance, appropriateness, and
applicability of these measure constructs.
Based on input from stakeholders, we have identified additional
concept areas for potential future measure development for the HH QRP.
These include claims-based within stay potentially preventable
hospitalization measures. The potentially preventable within-stay
hospitalization measures will look at the percentage of HH episodes in
which patients were admitted to an acute care hospital or seen in an
emergency department for a potentially preventable condition during an
HH episode. We solicited feedback on the importance, relevance,
appropriateness, and applicability of these measure constructs.
In alignment with the requirements of the IMPACT Act to develop
quality measures and standardize data for comparative purposes, we
believe that evaluating outcomes across the post-acute settings using
standardized data is an important priority. Therefore, in addition to
proposing a process-based measure for the domain of ``Functional
status, cognitive function, and changes in function and cognitive
function'', included in the proposed rule, we noted that we also
intended to develop outcomes-based quality measures, including
functional status and other quality outcome measures to further satisfy
this domain.
Comment: Three commenters expressed general support for the
measures under consideration for future years. These commenters stated
that measures should be tested in the home health setting prior to
being finalized, highlighting that the home setting is different than
other standardized institutional care settings and presents unique
challenges to caregivers and beneficiaries. One of the commenters
stated that the measurement domains are critically important in the
home health setting and highly relevant, especially for patients whose
goal is improvement, adding that the relevance, appropriateness, and
applicability can only be discussed after validity and reliability
testing is completed in the home health setting. Another commenter
suggested leveraging changes in quality measures as an effort to
safeguard the delivery of therapy services and ensure accountability on
the part of the provider.
Response: We appreciate the recommendations and comments. We agree
that all future measures should be adequately tested and found reliable
for the home health setting.
Comment: Commenters supported the development of functional status
measures. MedPAC also supported measures that cut-across sectors, as
long as they are standardized, and noted they would support the self-
care and mobility measure concepts for HHAs based on the IRF measure
specifications, as long as CMS ensured that the measures are aligned
across PAC settings. A few commenters recommended that functional
measures may assess for beneficiaries who do not have the goal of
improvement. Other commenters noted that stabilization measures are
appropriate for quality improvement initiatives as they closely align
with the goal of HH services to help patients maintain their current
level of function or when possible to improve it. Another commenter
suggested closely monitoring functional status measures to determine
the impact of other reforms, such as changes to the payment approaches,
to determine the impact of these changes on patient outcomes.
Response: We appreciate the comments from MedPAC and others. We
agree that the maintenance of function and avoidance or reduction in
functional decline are appropriate goals for HH patients. We appreciate
all recommendations and will take these comments into consideration as
we consider measures for future rulemaking.
Comment: Three commenters specifically supported the potentially
preventable within-stay hospitalization measure. MedPAC supported the
development of a claims-based, potentially preventable hospitalization
measure, adding that measuring potentially preventable hospitalizations
holds providers accountable only for conditions that generally could
have been managed by the HHA.
Response: We appreciate the comments from MedPAC and others
pertaining to the potentially preventable within-stay hospitalization
measure under consideration for future implementation in the HH QRP. We
note that appropriately assessing hospital readmissions as an outcome
is important, acknowledge the importance of avoiding unintended
consequences that may arise from such assessments, and will take into
consideration the commenters' recommendations.
Comment: Commenters had suggestions for other measures that could
be added to the HH QRP.
Response: We appreciate the commenters' recommendations and will
[[Page 51731]]
take them into account in our future measure development work.
1. IMPACT Act Implementation Update
As a result of the input and suggestions provided by technical
experts at the TEPs held by our measure developer, we noted in the
proposed rule that we are engaging in additional development work for
two measures that will satisfy section 1899B(c)(1)(E) of the Act,
including performing additional testing. We noted that we intended to
specify these measures under section 1899B(c)(1)(E) of the Act no later
than January 1, 2019 and we intend to propose to adopt them for the CY
2021 HH QRP, with data collection beginning on or about January 1,
2020.
We did not receive any comments on this update.
H. Standardized Patient Assessment Data
1. Standardized Patient Assessment Data Reporting for the CY 2019 HH
QRP
Section 1895(b)(3)(B)(v)(IV)(bb) of the Act requires that for
calendar years beginning on or after January 1, 2019, HHAs submit to
the Secretary standardized patient assessment data required under
section 1899B(b)(1) of the Act.
In the CY 2018 HH PPS proposed rule (82 FR 35351) we proposed that
the current pressure ulcer measure, Application of Percent of Residents
or Patients with Pressure Ulcers That Are New or Worsened (Short Stay)
(NQF #0678), be replaced with the proposed pressure ulcer measure,
Changes in Skin Integrity Post-Acute Care: Pressure Ulcer/Injury,
beginning with the CY 2020 HH QRP. The current pressure ulcer measure
will remain in the HH QRP until that time. Accordingly, for the
requirement that HHAs report standardized patient assessment data for
the CY 2019 HH QRP, we proposed that the data elements used to
calculate that measure meet the definition of standardized patient
assessment data for medical conditions and co-morbidities under section
1899B(b)(1)(B)(iv) of the Act, and that the successful reporting of
that data under section 1895(b)(3)(b)(v)(IV)(aa) of the Act for the
beginning of the HH episode (for example, HH start of care/resumption
of care), as well as the end of the HH episode (discharges) occurring
during the first two quarters of CY 2018 will also satisfy the
requirement to report standardized patient assessment data beginning
with the CY 2019 HH QRP.
The collection of assessment data pertaining to skin integrity,
specifically pressure related wounds, is important for multiple
reasons. Clinical decision making, care planning, and quality
improvement all depend on reliable assessment data collection. Pressure
related wounds represent poor outcomes, are a serious medical condition
that can result in death and disability, are debilitating and painful,
and are often avoidable.\94\ \95\ \96\ \97\ \98\ \99\ Pressure related
wounds are considered healthcare acquired conditions.
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\94\ Casey, G. (2013). ``Pressure ulcers reflect quality of
nursing care.'' Nurs N Z 19(10): 20-24.
\95\ Gorzoni, M.L. and S.L. Pires (2011). ``Deaths in nursing
homes.'' Rev Assoc Med Bras 57(3): 327-331.
\96\ Thomas, J.M., et al. (2013). ``Systematic review: Health-
related characteristics of elderly hospitalized adults and nursing
home residents associated with short-term mortality.'' J Am Geriatr
Soc 61(6): 902-911.
\97\ White-Chu, E.F., et al. (2011). ``Pressure ulcers in long-
term care.'' Clin Geriatr Med 27(2): 241-258.
\98\ Bates-Jensen BM. Quality indicators for prevention and
management of pressure ulcers in vulnerable elders. Ann Int Med.
2001;135 (8 Part 2), 744-51.
\99\ Bennet, G, Dealy, C Posnett, J (2004). The cost of pressure
ulcers in the UK, Age and Aging, 33(3):230-235.
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As we noted, the data elements needed to calculate the current
pressure ulcer measure are already included on the OASIS data set and
reported by HHAs, and exhibit validity and reliability for use across
PAC providers. Item reliability for these data elements was also tested
for the nursing home setting during implementation of MDS 3.0. Testing
results are from the RAND Development and Validation of MDS 3.0
project.\100\ The RAND pilot test of the MDS 3.0 data elements showed
good reliability and are applicable to the OASIS because the data
elements tested are the same as those used in the OASIS Data Set.
Across the pressure ulcer data elements, the average gold-standard
nurse to gold-standard nurse kappa statistic was 0.905. The average
gold-standard nurse to facility-nurse kappa statistic was 0.937. Data
elements used to risk adjust this quality measure were also tested
under this same pilot test, and the gold-standard to gold-standard
kappa statistic, or percent agreement (where kappa statistic not
available), ranged from 0.91 to 0.99 for these data elements. These
kappa scores indicate ``almost perfect'' agreement using the Landis and
Koch standard for strength of agreement.\101\
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\100\ Saliba, D., & Buchanan, J. (2008, April). Development and
validation of a revised nursing home assessment tool: MDS 3.0.
Contract No. 500-00-0027/Task Order #2. Santa Monica, CA: Rand
Corporation. Retrieved from https://www.cms.hhs.gov/NursingHomeQualityInits/Downloads/MDS30FinalReport.pdf.
\101\ Landis, R., & Koch, G. (1977, March). The measurement of
observer agreement for categorical data. Biometrics 33(1), 159-174.
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The data elements used to calculate the current pressure ulcer
measure received public comment on several occasions, including when
that measure was proposed in the CY 2016 HH PPS (80 FR 68623). Further,
they were discussed in the past by TEPs held by our measure development
contractor on June 13 and November 15, 2013, and recently by a TEP on
July 18, 2016. TEP members supported the measure and its cross-setting
use in PAC. The report, Technical Expert Panel Summary Report:
Refinement of the Percent of Patients or Residents with Pressure Ulcers
that are New or Worsened (Short-Stay) (NQF #0678) Quality Measure for
Skilled Nursing Facilities (SNFs), Inpatient Rehabilitation Facilities
(HHAs), Long-Term Care Hospitals (LTCHs), and Home Health Agencies
(HHAs), is available at and https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/Post-Acute-Care-Quality-Initiatives/IMPACT-Act-of-2014/IMPACT-Act-Downloads-and-Videos.html.
Comment: Some commenters supported reporting the data elements
already implemented in the HH QRP to fulfill the requirement to report
standardized patient assessment data for the CY 2019 HH QRP.
Specifically, the commenters supported the use of data elements used in
calculation of the Percent of Residents or Patients with Pressure
Ulcers That Are New or Worsened (Short Stay) (NQF #0678) to fulfill
this requirement. However, one commenter recommended that CMS implement
such measures after public deliberation and discussion. A commenter
suggested that CMS adopt the same policies in this CY 2018 HH PPS final
rule as it adopted for IRFs, SNFs and LTCHs in the other final rules
issued this year.
Response: We appreciate the support and where possible we have
aligned with the other settings. We affirm that as we continue to
implement measures, such as the pressure ulcer quality measure, we will
continue to engage the public both during the measure development phase
and through the rulemaking process.
Final Decision: After consideration of the public comments
received, we are finalizing as proposed that the data elements
currently reported by HHAs to calculate the current measure, Percent of
Residents or Patients with Pressure Ulcers That Are New or Worsened
(Short Stay) (NQF #0678),to meet the definition of standardized patient
assessment data with respect to medical conditions and co-morbidities
under section 1899B(b)(1)(B)(iv) of the Act,
[[Page 51732]]
and that the successful reporting of that data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will also satisfy the requirement
to report standardized patient assessment data under section
1895(b)(3)(B)(v)(IV)(bb) of the Act beginning with the CY 2019 HH QRP.
2. Standardized Patient Assessment Data Reporting Beginning With the CY
2020 HH QRP
In the CY 2018 HH PPS proposed rule (82 FR 35355 through 35371), we
described our proposals for the reporting of standardized patient
assessment data by HHAs beginning with the CY 2020 HH QRP. LTCHs, IRFs,
and SNFs are also required to report standardized patient assessment
data through their applicable PAC assessment instruments, and they do
so by responding to identical assessment questions developed for their
respective settings using an identical set of response options (which
incorporate an identical set of definitions and standards). We proposed
that HHAs will be required to report these data at admission (SOC/ROC)
and discharge beginning on January 1, 2019, with the exception of three
data elements (Brief Interview of Mental Status (BIMS), Hearing, and
Vision) that will be required at SOC/ROC only. Following the initial
reporting year (which will be based on 6 months of data) for the CY
2020 HH QRP, subsequent years for the HH QRP would be based on a full
calendar year of such data reporting.
In selecting the data elements, we carefully weighed the balance of
burden in assessment-based data collection and aimed to minimize
additional burden through the utilization of existing data in the
assessment instruments. We also noted that the patient and resident
assessment instruments are considered part of the medical record and
sought the inclusion of data elements relevant to patient care.
We also took into consideration the following factors for each data
element: overall clinical relevance; ability to support clinical
decisions, care planning, and interoperable exchange to facilitate care
coordination during transitions in care; and the ability to capture
medical complexity and risk factors that can inform both payment and
quality. In addition, the data elements had to have strong scientific
reliability and validity; be meaningful enough to inform longitudinal
analysis by providers; had to have received general consensus agreement
for its usability; and had to have the ability to collect such data
once but support multiple uses. Further, to inform the final set of
data elements for proposal, we took into account technical and clinical
subject matter expert review, public comment, and consensus input in
which such principles were applied.
We received several comments related to the reporting of the
standardized patient assessment data.
Comment: Many commenters expressed significant concerns with
respect to our standardized patient assessment data proposals. Several
commenters stated that the new standardized patient assessment data
reporting requirements will impose significant burden on providers,
given the volume of new standardized patient assessment data elements
that we proposed to add to the OASIS. Several commenters noted that the
addition of the proposed standardized patient assessment data elements
will require hiring more staff, retraining staff on revised questions
or coding guidance, and reconfiguring internal databases and EHRs.
Other commenters expressed concerns about the gradual but significant
past and future expansion of the OASIS through the addition of
standardized patient assessment data elements and quality measures,
noting the challenge of coping with ongoing additions and changes.
Several commenters expressed concern related to the implementation
timeline in the proposed rule. Several commenters noted that CMS had
not yet provided sufficient specifications or educational materials to
support implementation of the new patient assessments in the proposed
timeline. A few commenters urged CMS to delay the reporting of new
standardized patient assessment data elements and to carefully assess
whether all of the proposed standardized patient assessment data
elements are necessary under the IMPACT Act.
Response: We understand the concerns raised by commenters that
finalizing our standardized patient assessment data proposals will
require HHAs to spend a significant amount of resources preparing to
report the data, including updating relevant protocols and systems and
training appropriate staff. We also recognize that we can meet our
obligation to require the reporting of standardized patient assessment
data for the categories described in section 1899B(b)(1)(B) of the Act
while simultaneously being responsive to these concerns. Therefore,
after consideration of the public comments we received on these issues,
we have decided that at this time, we will not finalize the
standardized patient assessment data elements we proposed for three of
the five categories under section 1899B(b)(1)(B) of the Act: Cognitive
Function and Mental Status; Special Services, Treatments, and
Interventions; and Impairments.
Although we believe that the proposed standardized patient
assessment data elements would promote transparency around quality of
care and price as we continue to explore reforms to the PAC payment
system, the data elements that we proposed for each of these categories
would have imposed a new reporting burden on HHAs. We agree that it
would be useful to evaluate further how to best identify the
standardized patient assessment data that would satisfy each of these
categories; would be most appropriate for our intended purposes
including payment and measure standardization; and can be reported by
HHAs in the least burdensome manner. As part of this effort, we intend
to conduct a national field test that allows for stakeholder feedback
and to consider how to maximize the time HHAs have to prepare for the
reporting of standardized patient assessment data in these categories.
We intend to make new proposals for the categories described in
sections 1899B(b)(1)(B)(ii), (iii) and (v) of the Act no later than in
the CY 2020 HH PPS proposed rule.
In this final rule, we are finalizing the standardized patient
assessment data elements that we proposed to adopt for the IMPACT Act
categories of Functional Status and Medical Conditions and Co-
Morbidities. Unlike the standardized patient assessment data that we
are not finalizing, the standardized patient assessment data that we
proposed for Medical Conditions Co-Morbidities category is already
required to calculate the Percent of Residents or Patients with
Pressure Ulcers That Are New or Worsened (NQF #0678) quality measure,
and the Changes in Skin Integrity Post-Acute Care: Pressure Ulcer/
Injury quality measure. We are finalizing the quality measure,
Application of Percent of Long-Term Care Hospital Patients with an
Admission and Discharge Functional Assessment and a Care Plan That
Addresses Function (NQF #2631), and the additional standardized patient
assessment data elements in Section GG to satisfy the category of
Functional Status.
Comment: Some commenters expressed support for the adoption of
standardized patient assessment data elements. Several of these
commenters expressed support for standardizing the definitions as well
as the implementation of the data collection effort. A few commenters
also supported CMS' goal of standardizing the
[[Page 51733]]
questions and responses across all PAC settings. Another commenter
approved of the efforts CMS is making to engage the PAC community on
the implementation of the IMPACT Act, including holding Special Open
Door Forums and Medicare Learning Network (MLN) Calls to communicate
with providers about expectations/timelines over five years. MedPAC
recognized the value of and need for a unified patient assessment
system for PAC as part of a potential unified payment system for PAC.
Response: We appreciate the support.
Comment: A few commenters stated that there is insufficient
evidence demonstrating the reliability and validity of the proposed
standardized patient assessment data elements. Several commenters
stated that the expanded standardized patient assessment data reporting
requirements have not yet been adequately tested to ensure they collect
accurate and useful data in the HHA setting.
Response: Our standardized patient assessment data elements were
selected based on a rigorous multistage process described in the CY
2018 HH PPS proposed rule (82 FR 35344). In addition, we believe that
the PAC PRD testing of many of these data elements provides good
evidence from a large, national sample of patients and residents in PAC
settings to support the use of these standardized patient assessment
data elements in and across PAC settings. However, as previously
explained, we have decided at this time not to finalize the proposals
for three of the five categories under section 1899B(b)(1)(B) of the
Act: Cognitive Function and Mental Status; Special Services,
Treatments, and Interventions; and Impairments. Prior to making new
proposals for these categories, we intend to conduct additional testing
to ensure that the standardized patient assessment data elements we
select are reliable, valid and appropriate for their intended use.
Comment: MedPAC suggested that CMS should be mindful that some data
elements, when used for risk adjustment, may be susceptible to provider
manipulation. MedPAC is concerned about the proposed elements such as
oxygen therapy, intravenous medications, and nutritional approaches
that may incentivize increased use of services. MedPAC supported the
inclusion of these care items when they are tied to medical necessity,
such as in previous MedPAC work, where patients were counted as using
oxygen services only if they have diagnoses that typically require the
use of oxygen. MedPAC encouraged CMS to take a similar approach in
measuring use of services that are especially discretionary. For some
data elements, MedPAC suggested that CMS consider requiring a physician
to attest that the reported service was reasonable and necessary and
include a statement adjacent to the signature line warning that filing
a false claim is subject to treble damages under the False Claims Act.
Response: We thank MedPAC for their support of the standardized
patient assessment data elements that are associated with medical
necessity. We appreciate their suggestions to mitigate the potential
for false data submission and the unintended consequence of use of
services that are not medically indicated.
Comment: While supporting the overall concept of standardization
across PAC settings, several commenters strongly believed that the home
health setting is different than institutional settings and urged CMS
to consider this. One of these commenters encouraged CMS to perform
testing specifically in the home health setting. Another commenter was
concerned about the use of some data elements because they were not
designed for the home health setting and require specialized training
to accurately administer. Several commenters emphasized the importance
of risk adjustment, with some stating that effective risk adjustment
will be an essential policy feature for home health agencies to
distinguish how patients and data collection in non-standardized
settings such as the beneficiary's home differ from institutional
settings.
Response: We acknowledge that the four PAC provider types each have
unique challenges and provide unique services and appreciate the
commenters' concerns specific to the home health setting and the
potential variation in services and populations. Because of this, we
conducted a thorough process of phased testing and stakeholder
consensus to ensure we considered items that are aligned across PAC
settings and are relevant to and feasible in each setting. However, for
the reasons previously explained, we have decided at this time not to
finalize the standardized patient assessment data elements we proposed
for three of the five categories under section 1899B(b)(1)(B) of the
Act.
A full discussion of the standardized patient assessment data
elements that we proposed to adopt for the categories described in
sections 1899B(b)(1)(B)(ii), (iii) and (v) of the Act can be found in
the CY 2018 HH PPS proposed rule (82 FR 35355 through 35371). In light
of our decision not to finalize our proposals with respect to these
categories, we are not going to address in this final rule the specific
technical comments that we received on these proposed standardized
patient assessment data elements. However, we appreciate the many
technical comments we did receive specific to each of these data
elements, and we will take them into consideration as we develop new
proposals for these categories. In this section, we discuss the
comments we received specific to the standardized patient assessment
data we proposed to adopt and are finalizing in this final rule, for
the categories of Functional Status and Medical Conditions and Co-
Morbidities.
3. Standardized Patient Assessment Data by Category
a. Functional Status Data
We proposed that the data elements that will be reported by HHAs to
calculate the measure, Application of Percent of Long-Term Care
Hospital Patients with an Admission and Discharge Functional Assessment
and a Care Plan That Addresses Function (NQF #2631), as described in
section V.F.2 of the proposed rule will also meet the definition of
standardized patient assessment data for functional status under
section 1899B(b)(1)(B)(i) of the Act, and that the successful reporting
of that data under section 1895(b)(3)(B)(v)(IV)(aa) of the Act will
also satisfy the requirement to report standardized patient assessment
data under section 1895(b)(3)(B)(v)(IV)(bb) of the Act. Details on the
data used to calculate this measure is discussed in section V.F.2. of
this final rule.
To further satisfy the requirements under section 1899B(b)(1)(B)(i)
of the Act and specifically our efforts to achieve standardized patient
assessment data pertaining to functional status, such as mobility and
self-care at admission to a PAC provider and before discharge from a
PAC provider, we also proposed to adopt the functional status data
elements that specifically address mobility and self-care as provided
in the Act. We noted that these data elements were also used to
calculate the function outcome measures implemented and/or proposed for
implementation in three other post-acute quality reporting programs to
which the IMPACT Act applies (Application of NQF #2633--Change in Self-
Care Score for Medical Rehabilitation Patients; Application of NQF
#2634--Change in Mobility Score for Medical Rehabilitation Patients;
Application of NQF #2635--Discharge Self-Care Score for Medical
Rehabilitation Patients; and Application
[[Page 51734]]
of NQF #2636--Discharge Mobility Score for Medical Rehabilitation
Patients).
To achieve standardization, we noted that we have implemented such
data elements, or sub-sets of the items, into the other post-acute care
patient/resident assessment instruments and we proposed that they also
meet the definition of standardized patient assessment data for
functional status under section 1899B(b)(1)(B)(i) of the Act, and that
the successful reporting of such data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will also satisfy the requirement
to report standardized patient assessment data under section
1895(b)(3)(B)(v)(IV)(bb) of the Act. These data elements currently are
collected in the Section GG: Functional Abilities and Goals located in
current versions of the MDS and the IRF-PAI assessment instruments.
As previously described, the patient assessment data that assess
for functional status are from the CARE Item Set. They were
specifically developed for cross-setting application and are the result
of consensus building and public input. Further, we received public
comment and input on these patient assessment data. Their reliability
and validity testing were conducted as part of CMS' Post-Acute Care
Payment Reform Demonstration, and we concluded that the functional
status items have acceptable reliability and validity. We referred the
reader to section V.F.2 of the proposed rule for a full description of
the CARE Item Set and description of the testing methodology and
results that are available in several reports. For more information
about this quality measure and the data elements used to calculate it,
we referred readers to the FY 2016 IPPS/LTCH PPS final rule (80 FR
49739 through 49747), the FY 2016 IRF PPS final rule (80 FR 47100
through 47111), and the FY 2016 SNF PPS final rule (80 FR 46444 through
46453).
Therefore, we proposed to adopt the functional status data elements
for the CY 2020 HH QRP, requiring HHAs to report these data starting on
January 1, 2019. We noted that this proposal would align with the
required reporting timeframe for the CY 2020 HH QRP. Following the
initial 2 quarters of reporting for the CY 2020 HH QRP, we proposed
that for subsequent years for the HH QRP, the reporting of standardized
patient assessment data would be based on 12 months of data reporting
beginning with July 1, 2019, through June 30, 2020 for the CY 2021 HH
QRP.
Comment: Several commenters, including MedPAC, supported the
collection of standardized patient assessment data across PAC settings.
Some commenters specifically addressed support for CMS' proposal that
data elements submitted to CMS to calculate the measure, Application of
Percent of Long-Term Care Hospital Patients with an Admission and
Discharge Functional Assessment and a Care Plan that Addresses Function
(NQF #2631), would also satisfy the requirement to report standardized
patient assessment data elements under section 1899B(b)(1)(B)(i) of the
Act addressing functional status, such as mobility and self-care at
admission to a PAC provider and before discharge from a PAC provider.
Response: We appreciate the commenters' support.
Comment: A commenter suggested that CMS use the functional
assessment item, GG0170C: Lying to sitting on the side of bed for
purposes of standardization.
Response: We do not believe that collecting only GG170C would be
sufficient for purposes of collecting standardized function data. We
need a larger subset of Section GG items to calculate one of the
measures that we are finalizing in this final rule, Application of
Percent of Long-Term Care Hospital Patients with an Admission and
Discharge Functional Assessment and a Care Plan That Addresses Function
(NQF #2631), which is already finalized for SNFs, LTCHs and IRFs.
Section GG in its entirety also meets the definition of standardized
patient assessment data with respect to function because it is
standardized across the four PAC settings. If we did not collect
Section GG in its entirety from HHAs, we would be collecting a
different set of function items from HHAs than we collect from other
PAC provider types.
Final Decision: After consideration of the public comments
received, we are finalizing that the data elements in Section GG:
Functional Abilities and Goals meet the definition of standardized
patient assessment data elements for functional status under section
1899B(b)(1)(B)(i) of the Act, specifically those Section GG
standardized patient assessment data elements that are used in the
quality measure, ``Percent of Long-Term Care Hospital Patients with an
Admission and Discharge Functional Assessment and a Care Plan that
Addresses Function (NQF #2631)'', and the additional standardized
functional status data elements in Section GG. We note that Section GG
includes item GG170Q, which we inadvertently omitted in the
specifications that accompanied the CY 2018 HH PPS proposed rule. The
Section GG data elements can be found in the Finalized Specifications
for HH QRP Quality Measures and Standardized Patient Assessment Data
Elements document available at: https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html. We are also finalizing that the data elements
needed to calculate the measure, Application of Percent of Long-Term
Care Hospital Patients with an Admission and Discharge Functional
Assessment and a Care Plan That Addresses Function (NQF #2631), meet
the definition of standardized patient assessment data elements for
functional status under section 1899B(b)(1)(B)(i) of the Act, and that
the successful reporting of that data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will also satisfy the requirement
to report standardized patient assessment data elements under section
1895(b)(3)(B)(v)(IV)(bb) of the Act.
b. Medical Condition and Comorbidity Data
We proposed that the data elements needed to calculate the current
measure, Percent of Residents or Patients with Pressure Ulcers That Are
New or Worsened (Short Stay) (NQF #0678), and that the proposed
measure, Changes in Skin Integrity Post-Acute Care: Pressure Ulcer/
Injury, meet the definition of standardized patient assessment data
element with respect to medical conditions and co-morbidities under
section 1899B(b)(1)(B)(iv) of the Act, and that the successful
reporting of that data under section 1895(b)(3)(B)(v)(IV)(aa) of the
Act will also satisfy the requirement to report standardized patient
assessment data under section 1895(b)(3)(B)(v)(IV)(bb) of the Act.
``Medical conditions and co-morbidities'' and the conditions
addressed in the standardized assessment patient data elements used in
the calculation and risk adjustment of these measures, that is, the
presence of pressure ulcers, diabetes, incontinence, peripheral
vascular disease or peripheral arterial disease, mobility, as well as
low body mass index (BMI), are all health-related conditions that
indicate medical complexity that can be indicative of underlying
disease severity and other comorbidities.
Specifically, the data elements used in the measure are important
for care planning and provide information pertaining to medical
complexity. Pressure ulcers are serious wounds representing poor
outcomes, and can
[[Page 51735]]
result in sepsis and death. Assessing skin condition, care planning for
pressure ulcer prevention and healing, and informing providers about
their presence in patient transitions of care are a customary and best
practice. Venous and arterial disease and diabetes are associated with
insufficient low blood flow, which may increase the risk of tissue
damage. These diseases commonly are indicators of factors that may
place individuals at risk for pressure ulcer development and are
therefore important for care planning. Low BMI, which may be an
indicator of underlying disease severity, may be associated with loss
of fat and muscle, resulting in potential risk for pressure ulcers due
to shearing. Bowel incontinence, and the possible maceration to the
skin associated, can lead to higher risk for pressure ulcers. In
addition, the bacteria associated with bowel incontinence can
complicate current wounds and cause local infection. Mobility is an
indicator of impairment or reduction in mobility and movement which is
a major risk factor for the development of pressure ulcers. These data
elements are important for care planning, transitions in services and
identifying medical complexities.
Comment: Commenters supported our proposal to use data elements
already implemented in the HH QRP to satisfy the requirement to report
standardized patient assessment data.
Response: We appreciate the support.
Final decision: After consideration of the public comments
received, we are finalizing as proposed that the data elements
currently reported by HHAs to calculate the current measure, Percent of
Residents or Patients with Pressure Ulcers That Are New or Worsened
(Short Stay) (NQF #0678), and the finalized measure, Changes in Skin
Integrity Post-Acute Care: Pressure Ulcer/Injury, meet the definition
of standardized patient assessment data for medical conditions and co-
morbidities under section 1899B(b)(1)(B)(iv) of the Act, and that the
successful reporting of that data under section
1895(b)(3)(B)(v)(IV)(aa) of the Act will also satisfy the requirement
to report standardized patient assessment data under section
1895(b)(3)(B)(v)(IV)(bb) of the Act.
We note that for purposes of meeting the requirements of the CY
2020 HH QRP, HHAs will be required to report the data elements needed
to calculate the current pressure ulcer measure for the last two
quarters of CY 2018 (July-December) and the data elements needed to
calculate the updated pressure ulcer measure for the first two quarters
of CY 2019 (January-June).
I. Form, Manner, and Timing of Data Submission Under the HH QRP
1. Start Date for Reporting Standardized Patient Assessment Data by New
HHAs
In the CY 2016 HH PPS final rule (80 FR 68703 through 68706), we
adopted timing for new HHAs to begin reporting data on quality measures
under the HH QRP. In the CY 2018 HH PPS proposed rule (82 FR 35371), we
proposed that new HHAs would be required to begin reporting
standardized patient assessment data on the same schedule.
Comment: One commenter supported our proposed policy to require
that new HHAs begin reporting standardized patient assessment data on
the same schedule that they are required to begin reporting data on
quality measures.
Response: We thank the commenter for the support.
Final Decision: After consideration of the comments we received, we
are finalizing our proposal that new HHAs will be required to begin
reporting standardized patient assessment data on the same schedule
that they are currently required to begin reporting other quality data
under the HH QRP.
2. Mechanism for Reporting Standardized Patient Assessment Data
Beginning With the CY 2019 HH QRP
Under our current policy, HHAs report data by completing applicable
sections of the OASIS, and submitting the OASIS to CMS through the
QIES, ASAP system. For more information on HH QRP reporting through the
QIES ASAP system, we referred readers to https://www.qtso.com/index.php. In addition to the data currently submitted on quality
measures as previously finalized and described in Table 18 of this
rule, in the CY 2018 HH PPS proposed rule (82 FR 35372), we proposed
that HHAs would be required to begin submitting the proposed
standardized patient assessment data for HHA Medicare and Medicaid
quality episodes that begin or end on or after January 1, 2019 using
the OASIS.
Further, we proposed that all standardized patient assessment data
elements would be collected at SOC/ROC using the OASIS item set, and
all except the Brief Interview for Mental Status (BIMS), Hearing, and
Vision data elements are or would be collected at discharge using the
OASIS item set. Details on the modifications and assessment collection
for the OASIS for the proposed standardized data are available at
https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html.
We invited public comment on these proposals.
Comment: We received a comment in support of the proposed
mechanisms for reporting standardized patient assessment in the same
manner as the quality measure data for assessment based data beginning
with the CY 2019 HH QRP.
Response: We thank the commenter for its support.
Final Decision: After consideration of the public comment received,
we are finalizing our policy as proposed to use the same data reporting
mechanism for the submission of the standardized patient assessment
data elements that is already used for reporting quality measure data
used in the HH QRP beginning with the CY 2019 HH QRP.
3. Schedule for Reporting Standardized Patient Assessment Data
Beginning With the CY 2019 HH QRP
In the CY 2018 HH PPS proposed rule (82 FR 35372) we proposed to
apply our current schedule for the reporting of measure data to the
reporting of standardized patient assessment data, beginning with the
CY 2019 HH QRP. Under that policy, except for the first program year
for which a measure is adopted, HHAs must report data on measures for
HHA Medicare and Medicaid quality episodes that occur during the 12-
month period (between July 1 and June 30) that applies to the program
year. For the first program year for which a measure is adopted, HHAs
are only required to report data on HHA Medicare and Medicaid quality
episodes that begin on or after January 1 and end up to and including
June 30 of the calendar year that applies to that program year. For
example, for the CY 2019 HH QRP, data on measures adopted for earlier
program years must be reported for all HHA Medicare and Medicaid
quality episodes that begin on or after July 1, 2017, and end on or
before June 30, 2018. However, data on new measures adopted for the
first time for the CY 2019 HH QRP program year must only be reported
for HHA Medicare and Medicaid quality episodes that begin or end during
the first two quarters of CY 2018. Tables 20 and 21 illustrate this
policy and its proposed application to the reporting of standardized
patient assessment data, using CY 2019 and CY 2020 as examples.
[[Page 51736]]
Table 20--Summary Illustration of Initial Reporting for Newly Adopted
Measures and Proposed Standardized Patient Assessment Data Reporting
Using CY Q1 and Q2 Data for the HH QRP *
------------------------------------------------------------------------
Proposed data submission
Proposed data collection/submission deadlines beginning with CY
reporting period * 2019 HH QRP *
------------------------------------------------------------------------
January 1, 2018-June 30, 2018.......... July 31, 2018.
------------------------------------------------------------------------
* We note that submission of the OASIS must also adhere to the HH PPS
deadlines.
- The term ``CY 2019 HH QRP'' means the calendar year for which the HH
QRP requirements applicable to that calendar year must be met in order
for a HHA to avoid a two percentage point reduction to its market
basket percentage when calculating the payment rates applicable to it
for that calendar year.
Table 21--Summary Illustration of Oasis 12 Month Data Reporting for
Measures and Proposed Standardized Patient Assessment Data Reporting for
the HH QRP *
------------------------------------------------------------------------
Proposed data submission
Proposed data collection/submission deadlines beginning with CY
reporting period * 2020 HH QRP * [supcaret]
------------------------------------------------------------------------
July 1, 2018-June 30, 2019............. July 31, 2019.
------------------------------------------------------------------------
* We note that submission of the OASIS must also adhere to the HH PPS
deadlines.
[supcaret] The term ``CY 2020 HH QRP'' means the calendar year for which
the HH QRP requirements applicable to that calendar year must be met
in order for a HHA to avoid a two percentage point reduction to its
market basket percentage when calculating the payment rates applicable
to it for that calendar year.
We invited comment on our proposal to extend our current policy
governing the schedule for reporting the quality measure data to the
reporting of standardized patient assessment data for the HH QRP
beginning with the CY 2019 HH QRP.
We did not receive any comments regarding this proposal.
Final Decision: We are finalizing our proposal as proposed to
extend our current policy governing the schedule for reporting the
quality measure data to the reporting of standardized patient
assessment data for the HH QRP beginning with the CY 2019 HH QRP.
4. Schedule for Reporting Quality Measures Beginning With the CY 2020
HH QRP
As discussed in section V.I. of this final rule, we are finalizing
the adoption of three quality measures beginning with the CY 2020 HH
QRP: Changes in Skin Integrity Post-Acute Care: Pressure Ulcer/Injury;
Application of The Percent of Residents Experiencing One or More Falls
with Major Injury (NQF #0674); and Application of Percent of Long-Term
Care Hospital Patients with an Admission and Discharge Functional
Assessment and a Care Plan That Addresses Function (NQF #2631). In the
CY 2018 HH PPS proposed rule (82 FR 35372), we proposed that HHAs would
report data on these measures using OASIS reporting that is submitted
through the QIES ASAP system. More information on OASIS reporting using
the QIES ASAP system is located at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/OASIS/DataSpecifications.html.
For the CY 2020 HH QRP, under our current policy HHAs will be
required to report these data for HHA Medicare and Medicaid quality
episodes that begin or end during the period from January 1, 2019, to
June 30, 2019. Beginning with the CY 2021 HH QRP, we proposed that HHAs
would will be required to submit data for the entire 12-month period
from July 1 to June 30. Further, for the purposes of measure
calculation, our policy was established in the CY 2017 HH PPS final
rule (81 FR76784) that data are utilized using calendar year timeframes
with review and correction periods.
Comment: A commenter supported the proposed schedule for reporting
the three new quality measures beginning with the CY 2020 QRP. However,
the commenter also suggested that there is a disparity in how home
health providers are reimbursed, which creates challenges for their
submission of the required data.
Response: We interpret the comment to be suggesting that Medicare
reimbursement rates for HH services, compared to Medicare rates for
post-acute care services furnished by different provider-types, may
affect the ability of HHAs to comply with the data reporting
requirements under the HH QRP. We are cognizant of the challenges of
data collection and we consider this when developing and adopting our
measures.
Final Decision: After consideration of the public comment received,
we are finalizing our policy as proposed for the Schedule for Reporting
the Quality Measures beginning with the CY 2020 HH QRP.
5. Input Sought for Data Reporting Related to Assessment Based Measures
We have received input suggesting that we expand the population for
quality measurement to include all patients regardless of payer.
Approximately 75 percent of home health expenditures in 2014 were made
by either Medicare or Medicaid and currently both Medicare and Medicaid
collect and report data for OASIS. We believe that expanding the
patient population for which OASIS collects data will allow us to
ensure data that is representative of quality provided to all patients
in the HHA setting, and therefore, allow us to better determine whether
HH Medicare beneficiaries receive the same quality of care that other
patients receive. We also appreciate that collecting quality data on
all patients regardless of payer source may create additional burden.
However, we have also received input that the effort to separate out
Medicare and Medicaid beneficiaries, who are currently reported through
OASIS, from other patients, creates clinical and work flow implications
with an associated burden too, and noted that we further appreciate
that it is common practice for HHAs to collect OASIS data on all
patients, regardless of payer source. Thus, we sought input on whether
we should require quality data reporting on all HH patients, regardless
of payer, where feasible--noting that because Medicare Part A claims
data are submitted only with respect to Medicare beneficiaries, claims-
based measures would continue to be calculated only for Medicare
beneficiaries. We would like to clarify that CMS sought comment on this
all payor topic and therefore there
[[Page 51737]]
is no proposed policy to finalize. We appreciate the comments received
and will take all recommendations into consideration.
Comment: Several commenters supported data collection on all
patients regardless of payor. One commenter requested that CMS provide
additional explanation of what the benefit would be to collecting OASIS
data on all patients regardless of payor. Several commenters stated
that the addition of OASIS reporting for all patients regardless of
payor will impose significant burden on HHAs. Some commenters noted
that they used separate assessment documents for patients who are
insured by private payors and that they used these assessments, in
part, to avoid the burden of OASIS. A few commenters suggested that the
collection of OASIS data on all patients regardless of payor could
result in healthcare professionals spending more time with
documentation and less time providing patient care. Some commenters
suggested that if CMS requires HHAs to submit OASIS assessments on all
patients, they might need to increase their staff hours, hire
additional staff and incur additional expenses.
Response: We continue to believe that the reporting of all-payor
data under the HH QRP would add value to the program and provide a more
accurate representation of the quality provided by HHAs. Although we
acknowledge the concerns raised by commenters regarding the potential
burden of reporting all-payer data and on the potential impact of such
a requirement for the HH QRP, we wish to clarify that under the HH
Conditions of Participation (42 CFR 484.55), each patient must receive,
and an HHA must provide, a patient-specific, comprehensive assessment
that accurately reflects the patient's current health status and
includes information that may be used to demonstrate the patient's
progress toward achievement of desired outcomes. The comprehensive
assessment must also incorporate the use of the current version of the
OASIS items, using the language and groupings of the OASIS items, as
specified by the Secretary.
Comment: We received several comments pertaining to the submission
requirements of the OASIS instrument. Some commenters suggested that
OASIS data was required for submission on only Medicare fee-for-service
beneficiaries, while other commenters stated that HHAs must complete
the OASIS for all Medicare and Medicaid patients. Another commenter
noted that the HH Conditions of Participation already apply to all
patients in a Medicare-certified HHA. Other commenters stated that they
did not know what patient populations must be given an OASIS
assessment.
Response: As previously discussed, for the purposes HH QRP, data
reporting on the OASIS includes all Medicare and Medicaid
beneficiaries. However, the comprehensive assessment must also
incorporate the collection of the current version of the OASIS items,
using the language and groupings of the OASIS items.
Comment: Several commenters stated concerns about the potential
impact of all-payor information on the HH QRP public reporting and on
the HHVBP model because private payors differ from CMS with regard to
care pathways, approval, and authorization processes. Some commenters
stated that private payors had proprietary information and that CMS
would exceed its authority if it required all-payor reporting.
Commenters also stated that some private insurers had different
requirements than CMS pertaining to the number of visits paid for by
such insurers, which would inhibit the agency in comparing performance
across HHAs.
Response: We acknowledge concerns raised for the HHVBP model and
the potential downstream impacts. With regard to the commenter
suggesting that private payors' patients would generate proprietary
information, we want to clarify that the OASIS is not a proprietary
instrument and therefore we do not believe that a requirement that HHAs
use the OASIS in compliance with our CoPs raises proprietary issues.
J. Other Provisions for the CY 2019 HH QRP and Subsequent Years
1. Application of the HH QRP Data Completion Thresholds to the
Submission of Standardized Patient Assessment Data Beginning With the
CY 2019 HH QRP
In the CY 2016 HH PPS final rule (80 FR 68703 through 68704), we
defined the pay-for-reporting performance system model that could
accurately measure the level of an HHA's submission of OASIS data based
on the principle that each HHA is expected to submit a minimum set of
two matching assessments for each patient admitted to their agency.
These matching assessments together create what is considered a quality
episode of care, consisting ideally of a SOC or ROC assessment and a
matching End of Care EOC assessment. EOC assessments comprise the
Discharge from Agency, Death at Home and Transfer to an Inpatient
Facility time points. For further information on successful submission
of OASIS assessments, types of assessments submitted by an HHA that fit
the definition of a quality assessment, defining the ``Quality
Assessments Only'' (QAO) formula, and implementing a pay-for-reporting
performance requirement over a 3-year period, please see the CY 2016 HH
PPS final rule (80 FR 68704 to 68705).
Additionally, we finalized the pay-for-reporting threshold
requirements in the CY 2016 HH PPS final rule. We finalized a policy
through which HHAs must score at least 70 percent on the QAO metric of
pay-for-reporting performance requirement for CY 2017 (reporting period
July 1, 2015, to June 30, 2016), 80 percent for CY 2018 (reporting
period July 1, 2016, to June 30, 2017) and 90 percent for CY 2019
(reporting period July 1, 2017, to June 30, 2018). An HHA that does not
meet this requirement for a calendar year will be subject to a two
percentage point reduction to the market basket percentage increase
that will otherwise apply for that calendar year. In the CY 2018 HH PPS
proposed rule (82 FR 35373), we proposed to apply the threshold
requirements established in the CY 2016 HH PPS rule to the submission
of standardized patient assessment data beginning with the CY 2019 HH
QRP.
Comment: Commenter provided feedback on the QAO standard which
requires that at least 90 percent of OASIS assessments be usable for
calculating quality measures or be subject to a 2-percentage point
reduction to the market basket update for CY 2019. One commenter agreed
with our proposal to apply the HH QRP data completion thresholds to the
submission of standardized patient assessment data beginning in the CY
2019 HH QRP. A commenter suggested that the proposed 90 percent
threshold is very high and may be difficult for small or rural
providers meet, and suggested changing this to 80 percent or higher.
Response: We disagree that the 90 percent threshold for CY 2019 is
too high or difficult for HHAs to meet.
The home health CoPs as codified (42 CFR 484.55) mandate use of the
OASIS data set. OASIS reporting was first implemented on July 19, 1999
and in 2007, we adopted mandatory OASIS reporting for quality reporting
purposes under section 1895(b)(3)(B)(v)(I) of the Act. Furthermore,
HHAs have been required to submit OASIS data as a condition of payment
of their Medicare claims since 2010. Since, HHAs have been required to
report OASIS data for
[[Page 51738]]
the last 18 years as a CoP in the Medicare program and as a condition
of payment of their Medicare claims for the past 7 years, our
establishment of a 90 percent threshold for OASIS reporting should not
place any new or additional burden on HHAs.
Final Decision: After consideration of the comments received, we
are finalizing our proposal as proposed to extend our current HH QRP
data completion requirements to the submission of standardized patient
assessment data.
2. HH QRP Submission Exception and Extension Requirements
Our experience with other QRPs has shown that there are times when
providers are unable to submit quality data due to extraordinary
circumstances outside their control (for example, natural, or man-made
disasters). Other extenuating circumstances are reviewed on a case-by-
case basis. In the CY 2018 HH QRP proposed rule (82 FR 35373), we
proposed to define a ``disaster'' as any natural or man-made
catastrophe which causes damages of sufficient severity and magnitude
to partially or completely destroy or delay access to medical records
and associated documentation. Natural disasters could include events
such as hurricanes, tornadoes, earthquakes, volcanic eruptions, fires,
mudslides, snowstorms, and tsunamis. Man-made disasters could include
such events as terrorist attacks, bombings, floods caused by man-made
actions, civil disorders, and explosions. A disaster may be widespread
and impact multiple structures or be isolated and impact a single site
only.
In certain instances of either natural or man-made disasters, an
HHA may have the ability to conduct a full patient assessment and
record and save the associated data either during or before the
occurrence of the extraordinary event. In this case, the extraordinary
event has not caused the agency's data files to be destroyed, but it
could hinder the HHA's ability to meet the QRP's data submission
deadlines. In this scenario, the HHA will potentially have the ability
to report the data at a later date, after the emergency has passed. In
such cases, a temporary extension of the deadlines for reporting might
be appropriate.
In other circumstances of natural or man-made disaster, an HHA may
not have had the ability to conduct a full patient assessment, or to
record and save the associated data before the occurrence of the
extraordinary event. In such a scenario, the agency may not have
complete data to submit to CMS. We believe that it may be appropriate,
in these situations, to grant a full exception to the reporting
requirements for a specific period of time.
We do not wish to penalize HHAs in these circumstances or to unduly
increase their burden during these times. Therefore, we proposed a
process for HHAs to request and for us to grant exceptions and
extensions for the reporting requirements of the HH QRP for one or more
quarters, beginning with the CY 2019 HH QRP, when there are certain
extraordinary circumstances outside the control of the HHA. When an
exception or extension is granted, we would not reduce the HHA's PPS
payment for failure to comply with the requirements of the HH QRP.
We proposed that if an HHA seeks to request an exception or
extension for the HH QRP, the HHA must request an exception or
extension within 90 days of the date that the extraordinary
circumstances occurred. The HHA may request an exception or extension
for one or more quarters by submitting a written request to CMS that
contains the information noted below, via email to the HHA Exception
and Extension mailbox at HHAPureConsiderations@cms.hhs.gov. Requests
sent to CMS through any other channel would not be considered as valid
requests for an exception or extension from the HH QRP's reporting
requirements for any payment determination.
The subject of the email must read ``HH QRP Exception or Extension
Request'' and the email must contain the all following information:
HHA CCN.
HHA name.
CEO or CEO-designated personnel contact information
including name, telephone number, email address, and mailing address
(the address must be a physical address, not a post office box).
HHA's reason for requesting an exception or extension.
Evidence of the impact of extraordinary circumstances,
including but not limited to photographs, newspaper and other media
articles.
A date when the HHA believes it will be able to again
submit HH QRP data and a justification for the proposed date.
We proposed that exception and extension requests would need to be
signed by the HHA's CEO or CEO-designated personnel, and that if the
CEO designates an individual to sign the request, the CEO-designated
individual would be able to submit such a request on behalf of the HHA.
Following receipt of the email, we would provide a: (1) Written
acknowledgement, using the contact information provided in the email,
to the CEO or CEO-designated contact notifying them that the request
has been received; and (2) a formal response to the CEO or any CEO-
designated HHA personnel, using the contact information provided in the
email, indicating our decision.
We stated that this proposal would not preclude us from granting
exceptions or extensions to HHAs that have not requested them when we
determine that an extraordinary circumstance, such as an act of nature,
affects an entire region or locale. If we were to make the
determination to grant an exception or extension to all HHAs in a
region or locale, we proposed to communicate this decision through
routine communication channels to HHAs and vendors, including, but not
limited to, issuing memos, emails, and notices on our HH QRP Web site
once it is available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HomeHealthQualityReporting-Reconsideration-and-Exception-and-Extension.html.
We also proposed that we may grant an exception or extension to
HHAs if we determine that a systemic problem with one of our data
collection systems directly affected the ability of the HHA to submit
data. Because we do not anticipate that these types of systemic errors
will happen often, we do not anticipate granting an exception or
extension on this basis frequently.
If an HHA is granted an exception, we would not require that the
HHA submit any measure data for the period of time specified in the
exception request decision. If we grant an extension to the original
submission deadline, the HHA would still remain responsible for
submitting quality data collected during the timeframe in question,
although we would specify a revised deadline by which the HHA must
submit this quality data.
We also proposed that any exception or extension requests submitted
for purposes of the HH QRP would apply to that program only, and not to
any other program we administer for HHAs such as survey and
certification. OASIS requirements, including electronic submission,
during Declared Public Health Emergencies can be found at FAQs I-5, I-
6, I-7, I-8 at https://www.cms.gov/Medicare/Provider-Enrollment-and-Certification/SurveyCertEmergPrep/downloads/AllHazardsFAQs.pdf.
We intend to provide additional information pertaining to
exceptions and extensions for the HH QRP, including any additional
guidance, on
[[Page 51739]]
the HH QRP Web site at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HomeHealthQualityReporting-Reconsideration-and-Exception-and-Extension.html.
In the CY 2018 HH PPS proposed rule (82 FR 35374), we proposed to
codify the HH QRP Submission Exception and Extension Requirements at
Sec. 484.250(d) of our regulations.
Comment: One commenter expressed support for the creation of an
exception and extension request process for HHAs that experience
disasters or other extraordinary circumstances.
Response: We thank the commenter for the comment and support.
Final Decision: After consideration of comments received, we are
finalizing the adoption of the policy as proposed for HH QRP Submission
Exception and Extension Requirements beginning with the CY 2019 HH QRP
and our decision to codify the HH QRP Submission Exception and
Extension Requirements at Sec. 484.250(d) of our regulations.
3. HH QRP Submission Reconsideration and Appeals Procedures
The HH QRP reconsiderations and appeals process was finalized in
the CY 2013 HH PPS final rule (77 FR 67096). At the conclusion of the
required quality data reporting and submission period, we review the
data received from each HHA during that reporting period to determine
if the HHA met the HH QRP reporting requirements. HHAs that are found
to be noncompliant with the HH QRP reporting requirements for the
applicable calendar year will receive a 2 percentage point reduction to
its market basket percentage update for that calendar year.
Similar to our other quality reporting programs, such as the SNF
QRP, the LTCH QRP, and the IRF QRP, we include an opportunity for the
providers to request a reconsideration of our initial noncompliance
determination. To be consistent with other established quality
reporting programs and to provide an opportunity for HHAs to seek
reconsideration of our initial noncompliance decision, in the CY 2018
HH PPS proposed rule (82 FR 35374 through 35375) we proposed a process
that enables an HHA to request reconsideration of our initial non-
compliance decision in the event that it believes that it was
incorrectly identified as being non-compliant with the HH QRP reporting
requirements for a particular calendar year.
For the CY 2019 HH QRP, and subsequent years, we proposed a HHA
would receive a notification of noncompliance if we determine that the
HHA did not submit data in accordance with the HH QRP reporting
requirements for the applicable CY. The purpose of this notification is
to put the HHA on notice that the HHA: (1) Has been identified as being
non-compliant with the HH QRP's reporting requirements for the
applicable calendar year; (2) will be scheduled to receive a reduction
in the amount of two percentage points to its market basket percentage
update for the applicable calendar year; (3) may file a request for
reconsideration if it believes that the finding of noncompliance is
erroneous, has submitted a request for an extension or exception that
has not yet been decided, or has been granted an extension or
exception; and (4) must follow a defined process on how to file a
request for reconsideration, which will be described in the
notification.
We stated that we would only consider requests for reconsideration
after an HHA has been found to be noncompliant.
Notifications of noncompliance and any subsequent notifications
from CMS would be sent via a traceable delivery method, such as
certified U.S. mail or registered U.S. mail, or through other
practicable notification processes, such as a report from CMS to the
provider as a Certification and Survey Provider Enhanced Reports
(CASPER) report, that will provide information pertaining to their
compliance with the reporting requirements for the given reporting
cycle or from the Medicare Administrative Contractors assigned to
process the provider's claims. To obtain the compliance reports, we
stated that HHAs must access the CASPER Reporting Application. HHAs can
access the CASPER Reporting application via their CMS OASIS System
Welcome page by selecting the CASPER Reporting link. The ``CASPER
Reports'' link will connect an HHA to the QIES National System Login
page for CASPER Reporting.
We proposed to disseminate communications regarding the
availability of compliance reports through routine channels to HHAs and
vendors, including, but not limited to issuing memos, emails, Medicare
Learning Network (MLN) announcements, and notices on our HH QRP Web
site once it is available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HomeHealthQualityReporting-Reconsideration-and-Exception-and-Extension.html.
We proposed that an HHA would have 30 days from the date of the
letter of noncompliance to submit to us a request for reconsideration.
This proposed time frame would allow us to balance our desire to ensure
that HHA s have the opportunity to request reconsideration with our
need to complete the process and provide HHAs with our reconsideration
decision in a timely manner. We proposed that an HHA may withdraw its
request at any time and may file an updated request within the proposed
30-day deadline. We also proposed that, in very limited circumstances,
we may grant a request by an HHA to extend the proposed deadline for
reconsideration requests. We stated that it would be the responsibility
of an HHA to request an extension and demonstrate that extenuating
circumstances existed that prevented the filing of the reconsideration
request by the proposed deadline.
We also proposed that as part of the HHA's request for
reconsideration, the HHA would be required to submit all supporting
documentation and evidence demonstrating full compliance with all HH
QRP reporting requirements for the applicable calendar year, that the
HHA has requested an extension or exception for which a decision has
not yet been made, that the HHA has been granted an extension or
exception, or has experienced an extenuating circumstance as defined in
section V.I.2. of this final rule, but failed to file a timely request
of exception. We proposed that we would not review any reconsideration
request that fails to provide the necessary documentation and evidence
along with the request.
We proposed that the documentation and evidence may include copies
of any communications that demonstrate the HHA's compliance with the HH
QRP, as well as any other records that support the HHA's rationale for
seeking reconsideration, but must not include any protected health
information (PHI). We stated that we intended to provide a sample list
of acceptable supporting documentation and evidence, as well as
instructions for HHAs on how to retrieve copies of the data submitted
to CMS for the appropriate program year in the future on our HH QRP Web
site at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HomeHealthQualityReporting-Reconsideration-and-Exception-and-Extension.html.
We proposed that an HHA wishing to request a reconsideration of our
initial noncompliance determination would be required to do so by
submitting an email to the following email address:
HHAPureConsiderations@cms.hhs.gov.
[[Page 51740]]
Any request for reconsideration submitted to us by an HHA would be
required to follow the guidelines outlined on our HH QRP Web site once
it is available once it is available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HomeHealthQualityReporting-Reconsideration-and-Exception-and-Extension.html.
All emails must contain a subject line that reads ``HH QRP
Reconsideration Request.'' Electronic email submission is the only form
of reconsideration request submission that will be accepted by us. We
proposed that any reconsideration requests communicated through another
channel including, but not limited to, U.S. Postal Service or phone,
would not be considered as a valid reconsideration request.
We proposed that a reconsideration request include the all of the
following information:
HHA CMS Certification Number (CCN).
HHA Business Name.
HHA Business Address.
The CEO contact information including name, email address,
telephone number, and physical mailing address; or the CEO-designated
representative contact information including name, title, email
address, telephone number and physical mailing address.
CMS identified reason(s) for noncompliance from the non-
compliance notification.
The reason(s) for requesting reconsideration.
We proposed that the request for reconsideration must be
accompanied by supporting documentation demonstrating compliance.
Following receipt of a request for reconsideration, we would provide an
email acknowledgment, using the contact information provided in the
reconsideration request, to the CEO or CEO-designated representative
that the request has been received. Once we have reached a decision
regarding the reconsideration request, an email would be sent to the
HHA CEO or CEO designated representative, using the contact information
provided in the reconsideration request, notifying the HHA of our
decision.
We also proposed that the notifications of our decision regarding
reconsideration requests may be made available through a traceable
delivery method, such as certified U.S. mail or registered U.S. mail or
through the use of CASPER reports. If the HHA is dissatisfied with the
decision rendered at the reconsideration level, the HHA may appeal the
decision to the PRRB under 42 CFR 405.1835. We believe the proposed
process is more efficient and less costly for CMS and for HHAs because
it decreases the number of PRRB appeals by resolving issues earlier in
the process. Additional information about the reconsideration process
including details for submitting a reconsideration request will be
posted in the future to our HH QRP Web site at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HomeHealthQualityReporting-Reconsideration-and-Exception-and-Extension.html.
In the CY 2018 HH PPS proposed rule (82 FR 35375), we proposed to
add the HH QRP Submission Reconsideration and Appeals Procedures at
Sec. Sec. 484.250(e) and (f) of our regulations.
Comment: One commenter expressed support for the submission
reconsideration and appeals procedures for HHAs.
Response: We thank the commenter for the comment and support.
Final Decision: After consideration of the public comments
received, we are finalizing as proposed the adoption of the policy for
HH QRP Submission Reconsideration and Appeals Procedures for the CY
2019 HH QRP and subsequent years, which will be codified at Sec.
484.250(e) and (f) of our regulations.
K. Policies Regarding Public Display of Quality Measure Data for the HH
QRP
Our home health regulations, at Sec. 484.250(a), require HHAs to
submit OASIS assessments and Home Health Care Consumer Assessment of
Healthcare Providers and Systems Survey[supreg] (HHCAHPS) data to meet
the quality reporting requirements of section 1895(b)(3)(B)(v) of the
Act. Section 1899B(g) of the Act requires that data and information of
provider performance on quality measures and resource use and other
measures be made publicly available beginning not later than 2 years
after the applicable specified ``application date''. In addition,
section 1895(b)(3)(B)(v)(III) of the Act requires the Secretary to
establish procedures for making data submitted under section
1895(b)(3)(B)(v)(II) of the Act available to the public, and section
1899B(g)(1) of the Act requires the Secretary to do the same with
respect to HHA performance on measures specified under sections
1899B(c)(1) and (d)(1) of the Act. Section 1895(b)(3)(B)(v)(III) of the
Act requires that the public reporting procedures for data submitted
under subclause (II) ensure that a HHA has the opportunity to review
the data that is to be made public with respect to it prior to such
data being made public. Under section 1899B(g)(2) of the Act, the
public reporting procedures for performance on measures under sections
1899B(c)(1) and (d)(1) of the Act must ensure, including through a
process consistent with the process applied under section
1886(b)(3)(B)(viii)(VII) of the Act, (which refers to public display
and review requirements in the Hospital Inpatient Quality Reporting
(Hospital IQR) Program), that a HHA has the opportunity to review and
submit corrections to its data and information that are to be made
public for the agency prior to such data being made public. We
recognize that public reporting of quality data is a vital component of
a robust quality reporting program and are fully committed to ensuring
that the data made available to the public are meaningful. Further, we
agree that measures for comparing performance across home health
agencies must be constructed from data collected in a standardized and
uniform manner.
In the CY 2017 HH PPS final rule (81 FR 76785 through 76786), we
finalized procedures that allow individual HHAs to review and correct
their data and information on IMPACT Act measures that are to be made
public before those measure data are made public. Information on how to
review and correct data on IMPACT Act measures that are to be made
public before those measure data are made public can be found on the HH
QRP Web site at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/Home-Health-Quality-Reporting-Requirements.html. We did not propose any changes to
these policies in the CY 2018 HH PPS proposed rule.
However, in the CY 2018 HH PPS proposed rule (82 FR 35375 and
35376), pending the availability of data, we proposed to publicly
report data beginning in CY 2019 for the following two assessment-based
measures: (1) Percent of Patients or Residents with Pressure Ulcers
that are New or Worsened (NQF #0678); and (2) Drug Regimen Review
Conducted with Follow-Up for Identified Issues--PAC HH QRP. Data
collection for these two assessment-based measures began on OASIS on
January 1, 2017. We proposed to publicly report data beginning in CY
2019 for these assessment-based measures based on four rolling quarters
of data, beginning with data collected for discharges in 2017.
We proposed to publicly report data beginning in CY 2019 for the
following
[[Page 51741]]
3 claims-based measures: (1) Medicare Spending Per Beneficiary--PAC HH
QRP; (2) Discharge to Community-PAC HH QRP; and (3) Potentially
Preventable 30-Day Post-Discharge Readmission Measure for HH QRP. As
adopted in the CY 2017 HH PPS final rule (81 FR 43773), for the MSPB-
PAC HH QRP measure, we will use 1 year of claims data beginning with CY
2016 claims data to inform confidential feedback reports for HHAs, and
CY 2017 claims data for public reporting for the HH QRP. For the
Discharge to Community--PAC HH QRP measure we will use 2 years of
claims data, beginning with CYs 2015 and 2016 claims data to inform
confidential feedback and CYs 2016 and 2017 claims data for public
reporting. For the Potentially Preventable 30-Day Post-Discharge
Readmission Measure for HH QRP, we will use 3 years of claims data,
beginning with CY 2014, 2015 and 2016 claims data to inform
confidential feedback reports for HHAs, and CY 2015, 2016 and 2017
claims data for public reporting.
Finally, we proposed to assign HHAs with fewer than 20 eligible
cases during a performance period to a separate category: ``The number
of patient episodes for this measure is too small to report,'' \102\ to
ensure the statistical reliability of the measures. If a HHA had fewer
than 20 eligible cases, the HHA's performance would not be publicly
reported for the measure for that performance period.
---------------------------------------------------------------------------
\102\ This language is currently available as Footnote #4 on
Home Health Compare (https://www.medicare.gov/HomeHealthCompare/Data/Footnotes.html).
Table 22--New HH QRP Measures Proposed for CY 2019 Public Display
------------------------------------------------------------------------
-------------------------------------------------------------------------
Proposed measures:
Percent of Residents or Patients with Pressure Ulcers that Are New
or Worsened (Short Stay) (NQF #0678).
Drug Regimen Review Conducted with Follow-Up for Identified Issues--
PAC HH QRP.
Potentially Preventable 30-Day Post-Discharge Readmission Measure
for HH QRP.
Discharge to Community--(PAC) HH QRP.
Medicare Spending Per Beneficiary (PAC) HH QRP.
------------------------------------------------------------------------
We invited public comments on these proposals for the public
display of quality data.
Comment: Commenters provide feedback regarding the public display
of quality measures beginning CY 2019 for data collected beginning CY
2017. One commenter questioned if the Medicare Spending Per
Beneficiary--PAC HH QRP measure includes spending data that is specific
to HH services or the total amount of Medicare spending for
beneficiaries specific to a defined timeframe. One commenter did not
support public reporting for the Discharge to Community--PAC HH QRP
measure based on the potential for providers to have incentives against
the appropriate use of hospice services in a patient-centered continuum
of care. Another commenter did not support publicly reporting the Drug
Regimen Review Conducted with Follow-Up for Identified Issues--PAC HH
QRP measure, stating that this measure is dependent on physician
response and is not a measure of HHA quality or performance. Finally, a
commenter suggested a dashboard of measures aligned across home health
quality initiatives, including star ratings, Home Health Compare and
the HH VBP demonstration.
Response: We appreciate the commenters' suggestions regarding the
public display of quality measures. As finalized in the CY 2017 rule,
the MSPB-PAC HH QRP measure episode is comprised of a treatment period
and an associated services period. The treatment period includes those
services that are provided directly by the HHA. The associated services
period is the time during which Medicare Part A and Part B services
that are not treatment services are counted towards the episode,
subject to certain exclusions, such as planned admissions and organ
transplants. More detailed specifications for the MSPB-PAC measures,
including the MSPB-PAC HH QRP measure, are available at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/HHQIQualityMeasures.html.
The Discharge to Community measure excludes patients discharged to
home or facility-based hospice care. Thus, discharges to hospice are
not considered discharges to community, but rather are excluded from
the measure calculation. We wish to also note that including 31-day
post-discharge mortality outcomes is intended to identify successful
discharges to community, and to avoid the potential unintended
consequence of inappropriate community discharges that bypass hospice
care. With respect to the public reporting of Drug Regimen Review
Conducted with Follow-Up for Identified Issues, the intent of the
measure is to capture timely follow up for all potential clinically
significant issues. We believe the timely review and follow up of
potentially clinically significant medication issues at every
assessment time period and across the patient's episode of care is
essential for providing the best quality care for patients, and that
this measure helps to ensure that high quality care services are
furnished and that patient harm is avoided.
With regard to the commenter's suggestion that we provide a
dashboard that communicates alignment across the measures, we will take
the commenter's suggestion under consideration.
Comment: We received several comments about the Quality of Patient
Care star ratings. One commenter noted increased administrative and
clinical costs HHAs incur to maintain or improve the number of stars
instead of focusing on improving the scores on individual quality
measures. Another commenter stated that poor performing home health
agencies could rate higher than their actual performance while good or
excellent agencies could rate lower than their actual performance due
to the way the data is calculated.
Response: We thank the commenters, but note that these comments
relate to issues for which we made no proposals in the CY 2018 HH
proposed rule. Therefore, we believe these comments to be outside the
scope of the proposed rule and will not address them here.
Final Decision: After considering the comments received, we are
finalizing our proposals regarding public display of quality measure
data in the HH QRP.
L. Mechanism for Providing Confidential Feedback Reports to HHAs
Section 1899B(f) of the Act requires the Secretary to provide
confidential feedback reports to post-acute care (PAC) providers on
their performance on the measures specified under subsections (c)(1)
and (d)(1) of section 1899B of the Act, beginning one year after the
specified application date that applies to such measures and PAC
[[Page 51742]]
providers. In the CY 2017 HH PPS final rule (81 FR 76702), we finalized
processes to allow HH providers the opportunity to review their data
and information using confidential feedback reports that will enable
HHAs to review their performance on the measures required under the HH
QRP. Information on how to obtain these and other reports available to
the HH QRP can be found at https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HomeHealthQualityInits/Home-Health-Quality-Reporting-Requirements.html. We did not propose any
changes to this policy.
M. Home Health Care CAHPS[supreg] Survey (HHCAHPS)
In the CY 2017 HH PPS final rule (81 FR 76787), we stated that the
home health quality measures reporting requirements for Medicare-
certified agencies includes the Home Health Care CAHPS[supreg]
(HHCAHPS) Survey for the Home Health Quality Reporting Program and
along with OASIS measures, HHCAHPS participation is required for the
Annual Payment Update (APU). In the CY 2017 HH PPS final rule, we
finalized the reporting requirements and the data submission dates for
the CY 2017-CY 2020 APU periods. We proposed to continue the HHCAHPS
requirements in future years for the continuous monthly data collection
and quarterly data submission of HHCAHPS data.
1. Background and Description of HHCAHPS
The HHCAHPS survey is part of a family of CAHPS[supreg] surveys
that asks patients to report on and rate their experiences with health
care. For more details about the HHCAHPS Survey please see 81 FR 76787
through 76788.
We stated in previous rules that Medicare-certified HHAs are
required to contract with an approved HHCAHPS survey vendor. This
requirement continues, and Medicare-certified agencies are required to
provide a monthly list of their HHCAHPS-eligible patients to their
respective HHCAHPS survey vendors. Home health agencies are not allowed
to influence their patients about how the HHCAHPS survey.
As previously required, new HHCAHPS survey vendors are required to
attend Introduction training, and current HHCAHPS vendors are required
to attend Update training conducted by CMS and the HHCAHPS Survey
Coordination Team. New HHCAHPS vendors need to pass a post-training
certification test. We have approximately 25 approved HHCAHPS survey
vendors. The list of approved HHCAHPS survey vendors is available at
https://homehealthcahps.org.
2. HHCAHPS Oversight Activities
We stated in prior final rules that all approved HHCAHPS survey
vendors are required to participate in HHCAHPS oversight activities to
ensure compliance with HHCAHPS protocols, guidelines, and survey
requirements. The purpose of the oversight activities is to ensure that
approved HHCAHPS survey vendors follow the HHCAHPS Protocols and
Guidelines Manual.
In the CY 2013 HH PPS final rule (77 FR 67095 through 67097,
67164), we codified at Sec. 484.250(c)(3) that all approved HHCAHPS
survey vendors are required to fully comply with all HHCAHPS oversight
activities.
In the CY 2018 HH PPS proposed rule (82 FR 35377), we restated the
HHCAHPS requirements for CY 2019, because participation occurs in the
period of the publication of the proposed and final rules for CY 2018.
We additionally presented the HHCAHPS requirements for CY 2020 for the
sake of continuity. We proposed the HHCAHPS requirements for the CY
2021 Annual Payment Update.
3. HHCAHPS Requirements for the CY 2019 HH QRP
In the CY 2017 HH PPS final rule (81 FR 76789), we finalized the
requirements for the CY 2019 HH QRP. For the CY 2019 HH QRP, we require
continuous monthly HHCAHPS data collection and reporting for four
quarters. The data collection period for the CY 2018 HH QRP includes
the second quarter 2017 through the first quarter 2018 (the months of
April 2017 through March 2018). HHAs will be required to submit their
HHCAHPS data files to the HHCAHPS Data Center for the second quarter
2017 by 11:59 p.m., eastern daylight time (e.d.t.) on October 19, 2017;
for the third quarter 2017 by 11:59 p.m., eastern standard time
(e.s.t.) on January 18, 2018; for the fourth quarter 2017 by 11:59
p.m., e.d.t. on April 19, 2018; and for the first quarter 2018 by 11:59
p.m., e.d.t. on July 19, 2018. These deadlines are firm; no exceptions
will be permitted.
For more details on the CY 2019 HH QRP, we refer readers to 81 FR
76789.
4. HHCAHPS Requirements for the CY 2020 HH QRP
In the CY 2017 HH PPS final rule (81 FR 76789), we finalized the
requirements for the CY 2020 HH QRP. For the CY 2020 HH QRP, we require
continued monthly HHCAHPS data collection and reporting for four
quarters. The data collection period for the CY 2020 HH QRP includes
the second quarter 2018 through the first quarter 2019 (the months of
April 2018 through March 2019). HHAs will be required to submit their
HHCAHPS data files to the HHCAHPS Data Center for the second quarter
2018 by 11:59 p.m., e.d.t. on October 18, 2018; for the third quarter
2018 by 11:59 p.m., e.s.t. on January 17, 2019; for the fourth quarter
2018 by 11:59 p.m., e.d.t. on April 18, 2019; and for the first quarter
2019 by 11:59 p.m., e.d.t. on July 18, 2019. These deadlines are firm;
no exceptions will be permitted.
For more details about the CY 2020 HH QRP, we refer readers to 81
FR 76789.
5. HHCAHPS Requirements for the CY 2021 HH QRP
For the CY 2021 HH QRP, we proposed to require the continued
monthly HHCAHPS data collection and reporting for four quarters. The
data collection period for the CY 2021 HH QRP includes the second
quarter 2019 through the first quarter 2020 (the months of April 2019
through March 2020). HHAs will be required to submit their HHCAHPS data
files to the HHCAHPS Data Center for the second quarter 2019 by 11:59
p.m., e.d.t. on October 17, 2019; for the third quarter 2019 by 11:59
p.m., e.s.t. on January 16, 2020; for the fourth quarter 2019 by 11:59
p.m., e.d.t. on April 16, 2020; and for the first quarter 2020 by 11:59
p.m., e.d.t. on July 16, 2020. These deadlines are firm; no exceptions
will be permitted.
For the CY 2021 HH QRP, we proposed to require that all HHAs with
fewer than 60 HHCAHPS-eligible unduplicated or unique patients in the
period of April 1, 2018 through March 31, 2019 are exempt from the
HHCAHPS data collection and submission requirements for the CY 2021 HH
QRP, upon completion of the CY 2021 HHCAHPS Participation Exemption
Request form, and upon CMS verification of the HHA patient counts.
Agencies with fewer than 60 HHCAHPS-eligible, unduplicated or unique
patients in the period of April 1, 2018 through March 31, 2019 were
proposed to be required to submit their patient counts on the CY 2021
HHCAHPS Participation Exemption Request form posted on https://homehealthcahps.org from April 1, 2019 to 11:59 p.m., e.d.t. to March
31, 2020. This deadline is firm, as are all of the quarterly data
submission deadlines for the HHAs that participate in HHCAHPS.
[[Page 51743]]
We proposed to automatically exempt HHAs receiving Medicare
certification on or after the start of the period in which HHAs do
their patient count for a particular year's HHCAHPS data submission
from the HHCAHPS reporting requirement for the year. We proposed that
HHAs receiving Medicare-certification on or after April 1, 2019 would
be exempt from the HHCAHPS reporting requirement for the CY 2021 HH
QRP. As we have finalized in previous years, we proposed that these
newly-certified HHAs do not need to complete the HHCAHPS Participation
Exemption Request Form for the CY 2021 HH QRP.
6. HHCAHPS Reconsiderations and Appeals Process
As finalized in previous rules, we proposed that HHAs must monitor
their respective HHCAHPS survey vendors to ensure that vendors submit
their HHCAHPS data on time, by accessing their HHCAHPS Data Submission
Reports on https://homehealthcahps.org. This helps HHAs ensure that
their data are submitted in the proper format for data processing to
the HHCAHPS Data Center.
We proposed to continue HHCAHPS oversight activities as finalized
in the previous rules. In the CY 2013 HH PPS final rule (77 FR 67068,
67164), we codified the current guideline that all approved HHCAHPS
survey vendors must fully comply with all HHCAHPS oversight activities.
We included this survey requirement at Sec. 484.250(c)(3).
For further information on the HH QRP reconsiderations and appeals
process, please see section V.J.3. of this final rule.
7. Summary
We did not propose any changes to the participation requirements,
or to the requirements pertaining to the implementation of the Home
Health CAHPS[supreg] Survey (HHCAHPS). We only proposed updates to the
information to reflect the dates for future HH QRP years. We encouraged
HHAs to keep up-to-date about the HHCAHPS by regularly viewing the
official Web site for the HHCAHPS at https://homehealthcahps.org. We
noted that HHAs can also send an email to the HHCAHPS Survey
Coordination Team at hhcahps@rti.org or to CMS at
homehealthcahps@cms.hhs.gov, or telephone toll-free (1-866-354-0985)
for more information about the HHCAHPS Survey.
Final Decision: We did not receive any comments on our proposals.
Accordingly, we are finalizing the proposals. We again strongly
encourage HHAs to keep up-to-date about the HHCAHPS by regularly
viewing the official Web site for the HHCAHPS at https://homehealthcahps.org. HHAs can also send an email to the HHCAHPS Survey
Coordination Team at hhcahps@rti.org or to CMS at
homehealthcahps@cms.hhs.gov, or telephone toll-free (1-866-354-0985)
for more information about the HHCAHPS Survey.
VI. Collection of Information Requirements
A. Statutory Requirement for Solicitation of Comments
Under the Paperwork Reduction Act of 1995 (PRA), we are required to
provide 60-day notice in the Federal Register and solicit public
comment before a collection of information requirement is submitted to
the OMB for review and approval. We note that we will submit a revised
information collection request (OMB control number 0938-1279) to OMB
for review. This will also extend the information collection request
which expires December 30, 2019. 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.
This final rule makes reference to associated information
collections that are not discussed in the regulation text contained in
this document.
B. Collection of Information Requirements for the HH QRP
We believe that the burden associated with the HH QRP is the time
and effort associated with data collection and reporting. As of April
1, 2017, there are approximately 12,149 HHAs reporting quality data to
CMS. For the purposes of calculating the costs associated with the
collection of information requirements, we obtained mean hourly wages
for these staff from the U.S. Bureau of Labor Statistics' May 2016
National Occupational Employment and Wage Estimates (https://www.bls.gov/oes/current/oes_nat.htm). To account for overhead and
fringe benefits (100 percent), we have doubled the hourly wage. These
amounts are detailed in Table 23.
Table 23--U.S. Bureau of Labor Statistics' May 2016 National Occupational Employment and Wage Estimates
----------------------------------------------------------------------------------------------------------------
Fringe Adjusted
Occupation title Occupation Mean hourly benefit hourly wage
code wage ($/hr) (100%) ($/hr) ($/hr)
----------------------------------------------------------------------------------------------------------------
Registered Nurse (RN)........................... 29-1141 $34.70 $34.70 $69.40
Physical therapists HHAs........................ 29-1123 46.42 46.42 92.84
Speech-Language Pathologists (SLP).............. 29-1127 37.60 37.60 75.20
Occupational Therapists (OT).................... 29-1122 40.25 40.25 80.50
----------------------------------------------------------------------------------------------------------------
The OASIS changes that we are finalizing in section V.D of this
final rule will result in the removal of 70 data elements from the
OASIS at the time point of Start of Care (SOC), 70 data elements at the
time point of Resumption of Care (ROC), 18 data elements at the time
point of Follow-up (FU), 42 data elements at the time point of Transfer
to an Inpatient Facility (TOC), 1 data element at the time point of
Death at Home (Death), and 34 data elements at the time point of
Discharge from Agency (Discharge). These data items will not be used in
the calculation of quality measures adopted in the HH QRP, or for other
purposes that are not related to the HH QRP.
Section V.F.1. of this final rule adopts a new pressure ulcer
measure to replace the current pressure ulcer measure that
[[Page 51744]]
we previously specified under section 1899B(c)(1)(B) of the Act,
beginning with the CY 2020 HH QRP. The replacement measure is entitled,
``Changes in Skin Integrity Post-Acute Care: Pressure Ulcer/Injury.''
The new measure will be calculated using data elements that are
currently collected and reported using the OASIS-C2 (version effective
January 1, 2017). Adoption of the Changes in Skin Integrity Post-Acute
Care: Pressure Ulcer/Injury measure will result in the removal of item
M1313, which has 6 data elements that cover the same issues that are
addressed in the pressure ulcer assessment that will be required under
the new pressure ulcer measure, making it duplicative and no longer
necessary to separately collect.
In sections V.F.2. of this final rule, we are adopting a new
quality measure under section 1899B(c)(1)(A) of the Act beginning with
the CY 2020 HH QRP entitled ``Application of Percent of Long-Term Care
Hospital Patients with an Admission and Discharge Functional Assessment
and a Care Plan That Addresses Function (NQF #2631).'' In the CY 2018
HH PPS proposed rule (82 FR 35379), we stated that if we finalized the
adoption of this measure, we would add 13 standardized patient
assessment data elements at SOC, 13 data elements at ROC, 15
standardized patient assessment data elements at FU, and 13
standardized patient assessment data elements at Discharge. We
inadvertently did not include in our original burden estimate two OASIS
items (GG0170Q and GG0170RR) that are needed to calculate this
measure.\103\ We have updated our burden estimate to include these
items, and note that as a result of finalizing this measure, we will be
adding 15 standardized patient assessment data elements at SOC, 15
standardized patient assessment data elements at ROC, 16 standardized
patient assessment data elements at FU, and 15 standardized patient
assessment data elements at Discharge.
In sections V.F.3. of this final rule, we are adopting a new
quality measure under section 1899B(c)(1)(D) of the Act beginning with
the CY 2020 HH QRP entitled ``Application of Percent of Residents
Experiencing One or More Falls with Major Injury (NQF# 0674).'' The new
measure will be calculated using new standardized data elements added
to the OASIS. Specifically, we are adding 4 data elements at TOC, 4
data elements at Death, and 4 data elements at Discharge.
In sections V.H.2 and V.H.3 of this final rule, we are finalizing
our proposal to collect standardized patient assessment data with
respect to the Medical Condition and Comorbidity category beginning
with the CY 2019 HH QRP and Functional Status beginning with the CY
2020 HH QRP. As a result, we are adding to the OASIS the standardized
patient assessment data elements associated with these categories,
which include 17 standardized patient assessment data elements at SOC,
17 standardized patient assessment data elements at ROC, and 12
standardized patient assessment data elements at Discharge.
We are not finalizing our proposals to require HHAs to report
standardized patient assessment data elements for three of the five
categories under section 1899B(b)(1)(B) of the Act: Cognitive Function
and Mental Status; Special Services, Treatments, and Interventions; and
Impairments. As a result, we will not be adding to the OASIS the data
elements associated with these proposals, which included 36 data
elements at SOC, 36 data elements at ROC, or 24 data elements at
discharge.
The OASIS instrument is used for both the HH QRP and the HH PPS. In
sections III.E. of this final rule, after receiving detailed comments
from the public we are not finalizing the implementation of the HHGM.
Therefore, we are not finalizing the proposal to add two current OASIS-
C2 items, M1033 and M1800, at the FU time point or to remove collection
of eight current OASIS-C2 integumentary status items at the FU time
point.
In summary, as a net result of the policies we are finalizing in
this final rule, we will be removing 38 data elements at SOC, 38 data
elements at ROC, 2 data elements at FU, 38 data elements at TOC and 9
data elements at Discharge. We will be adding 3 data elements at Death.
Under section 1899B(m) of the Act, the Paperwork Reduction Act does
not apply to section 1899B, or to the sections of the OASIS that
require modification to achieve the standardization of patient
assessment data. We are, however, setting out the burden as a courtesy
to advise interested parties of the actions' time and costs and for
reference in the regulatory impact analysis (RIA) section VII. of this
final rule. The requirement and burden will be submitted to OMB for
review and approval when the modifications to the OASIS have achieved
standardization and are no longer exempt from the requirements under
section 1899B(m) of the Act.
We assume that each data element requires 0.3 minutes of clinician
time to complete. Therefore, there is a reduction in clinician burden
per OASIS assessment of 11.4 minutes at SOC, 11.4 minutes at ROC, 0.6
minutes at FU, 11.4 minutes at TOC 2.7 minutes at Discharge. There is
an increase in clinician burden per assessment of 0.9 minutes at Death.
The OASIS is completed by RNs or PTs, or very occasionally by
occupational therapists (OT) or speech language pathologists (SLP/ST).
Data from 2016 show that the SOC/ROC OASIS is completed by RNs
(approximately 87 percent of the time), PTs (approximately 12.7 percent
of the time), and other therapists, including OTs and SLP/STs
(approximately 0.3 percent of the time). Based on this analysis, we
estimated a weighted clinician average hourly wage of $72.40, inclusive
of fringe benefits, using the hourly wage data in Table 23. Individual
providers determine the staffing resources necessary.
Table 24 shows the total number of assessments submitted in CY 2016
and estimated burden at each time point.
Table 24--CY 2016 OASIS Submissions and Estimated Burden, by Time Point
------------------------------------------------------------------------
CY 2016
Time point assessments Estimated burden
completed ($)
------------------------------------------------------------------------
Start of Care..................... 6,261,934 -$86,139,164.10
Resumption of Care................ 1,049,247 -14,443,441.73
Follow-up......................... 3,797,410 -2,749,324.84
Transfer to an inpatient facility. 1,892,099 -26,027,713.84
Death at Home..................... 41,128 44,665.01
Discharge from agency............. 5,120,124 -16,681,363.99
-------------------------------------
[[Page 51745]]
Total......................... 18,161,942 -145,986,343.50
------------------------------------------------------------------------
* Estimated Burden ($) at each Time-Point = (# CY 2016 Assessments
Completed) x (clinician burden [min]/60) x ($72.40 [weighted clinician
average hourly wage]).
Based on the data in Table 24, for the 12,149 active Medicare-
certified HHAs in April 2017, we estimate the total average decrease in
cost associated with changes to the HH QRP at $12,016.33 per HHA
annually, or $145,986,343.50 for all HHAs annually. This corresponds to
an estimated reduction in clinician burden associated with changes to
the HH QRP of 166 hours per HHA annually, or 2,016,386 hours for all
HHAs annually. This decrease in burden will be accounted for in the
information collection under OMB control number 0938-1279.
C. Submission of PRA-Related Comments
We have submitted a copy of this final rule to OMB for its review
of the rule's information collection and recordkeeping requirements.
The requirements are not effective until they have been approved by
OMB.
To obtain copies of a supporting statement and any related forms
for the proposed collection(s) summarized in this notice, you may make
your request using one of following:
1. Access CMS' Web site address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at (410) 786-1326.
See this final rule's DATES and ADDRESSES sections for the comment
due date and for additional instructions.
VII. Regulatory Impact Analysis
A. Statement of Need
Section 1895(b)(1) of the Act requires the Secretary to establish a
HH PPS for all costs of home health services paid under Medicare. In
addition, section 1895(b) of the Act requires: (1) The computation of a
standard prospective payment amount include all costs for home health
services covered and paid for on a reasonable cost basis and that such
amounts be initially based on the most recent audited cost report data
available to the Secretary; (2) the prospective payment amount under
the HH PPS to be an appropriate unit of service based on the number,
type, and duration of visits provided within that unit; and (3) the
standardized prospective payment amount be adjusted to account for the
effects of case-mix and wage levels among HHAs. Section 1895(b)(3)(B)
of the Act addresses the annual update to the standard prospective
payment amounts by the HH applicable percentage increase. Section
1895(b)(4) of the Act governs the payment computation. Sections
1895(b)(4)(A)(i) and (b)(4)(A)(ii) of the Act require the standard
prospective payment amount to be adjusted for case-mix and geographic
differences in wage levels. Section 1895(b)(4)(B) of the Act requires
the establishment of appropriate case-mix adjustment factors for
significant variation in costs among different units of services.
Lastly, section 1895(b)(4)(C) of the Act requires the establishment of
wage adjustment factors that reflect the relative level of wages, and
wage-related costs applicable to home health services furnished in a
geographic area compared to the applicable national average level.
Section 1895(b)(3)(B)(iv) of the Act provides the Secretary with
the authority to implement adjustments to the standard prospective
payment amount (or amounts) for subsequent years to eliminate the
effect of changes in aggregate payments during a previous year or years
that was the result of changes in the coding or classification of
different units of services that do not reflect real changes in case-
mix. Section 1895(b)(5) of the Act provides the Secretary with the
option to make changes to the payment amount otherwise paid in the case
of outliers because of unusual variations in the type or amount of
medically necessary care. Section 1895(b)(3)(B)(v) of the Act requires
HHAs to submit data for purposes of measuring health care quality, and
links the quality data submission to the annual applicable percentage
increase.
The HHVBP Model will apply a payment adjustment based on an HHA's
performance on quality measures to test the effects on quality and
expenditures.
B. Overall Impact
We have examined the impacts of this final 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), the Regulatory Flexibility Act (RFA)
(September 19, 1980, Pub. L. 96-354), section 1102(b) of the Act,
section 202 of the Unfunded Mandates Reform Act of 1995 (UMRA, March
22, 1995; Pub. L. 104-4), Executive Order 13132 on Federalism (August
4, 1999), the Congressional Review Act (5 U.S.C. 804(2) and Executive
Order 13771 on Reducing Regulation and Controlling Regulatory Costs
(January 30, 2017).
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). We
included a detailed alternatives considered section in the CY 2018 HH
PPS proposed rule, which outlined alternatives considered for the CY
2018 HH PPS payment update, the proposed HHGM, and HH VBP model (82 FR
35388 and 35389).
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 $100 million or more in
any 1 year, or adversely and materially affecting a sector of the
economy, productivity, competition, jobs, the environment, public
health or safety, or state, local or tribal governments or communities
(also referred to as ``economically significant''); (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 novel
legal or policy issues arising out of legal mandates, the President's
priorities, or the principles set forth in the Executive Order.
[[Page 51746]]
A regulatory impact analysis (RIA) must be prepared for major rules
with economically significant effects ($100 million or more in any 1
year). The savings impacts related to the HHVBP Model as a whole are
estimated at a total projected 5-year gross savings of $378 million
assuming a savings estimate of a 6 percent annual reduction in
hospitalizations and a 1.0 percent annual reduction in SNF admissions;
the portion attributable to this final rule is negligible. In section
VII. of this final rule, we identified a reduction in our regulatory
reporting burden of $ 145,986,343.50. We estimate that this rulemaking
is ``economically significant'' as measured by the $100 million
threshold, and hence also a major rule under the Congressional Review
Act. Accordingly, we have prepared a Regulatory Impact Analysis that,
to the best of our ability, presents the costs and benefits of the
rulemaking.
In addition, section 1102(b) of the Act requires us to prepare a
RIA 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 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. This rule is applicable exclusively to HHAs. Therefore,
the Secretary has determined this final rule will not have a
significant economic impact on the operations of small rural hospitals.
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 2017, that
threshold is approximately $148 million. This final rule is not
anticipated to have an effect on State, local, or tribal governments,
in the aggregate, or on the private sector of $148 million or more.
If regulations impose administrative costs on private entities,
such as the time needed to read and interpret this final rule, we must
estimate the cost associated with regulatory review. Due to the
uncertainty involved with accurately quantifying the number of entities
that will review the rule, we assume that the total number of unique
commenters on this year's proposed rule will be the number of reviewers
of this final 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 this year's rule in detail, and it is
also possible that some reviewers chose not to comment on the proposed
rule. For these reasons we believe that the number of commenters will
be a fair estimate of the number of reviewers of this final rule.
We also recognize that different types of entities are in many
cases affected by mutually exclusive sections of this proposed rule,
and therefore for the purposes of our estimate we assume that each
reviewer reads approximately 50 percent of the rule.
Using the 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 $105.16 per hour, including overhead and fringe
benefits (https://www.bls.gov/oes/2016/may/naics4_621100.htm). Assuming
an average reading speed, we estimate that it will take approximately
2.6 hours for the staff to review half of this final rule. For each HHA
that reviews the rule, the estimated cost is $273.42 (2.6 hours x
$105.16). Therefore, we estimate that the total cost of reviewing this
regulation is $368,023.32 ($273.42 x 1,346 reviewers).
1. HH PPS for CY 2018
The update set forth in this final rule applies to Medicare
payments under HH PPS in CY 2018. Accordingly, the following analysis
describes the impact in CY 2018 only. We estimate that the net impact
of the policies in this final rule is approximately $80 million in
decreased payments to HHAs in CY 2018. We applied a wage index budget
neutrality factor and a case-mix weights budget neutrality factor to
the rates as discussed in section III.C.3. of this final rule.
Therefore, the estimated impact of the 2018 wage index and the
recalibration of the case-mix weights for 2018 is zero. The -$80
million impact reflects the distributional effects of a 0.5 percent
reduction in payments due to the sunset of the rural add-on provision
($100 million decrease), a 1 percent home health payment update
percentage ($190 million increase), and a -0.97 percent adjustment to
the national, standardized 60-day episode payment rate to account for
nominal case-mix growth for an impact of -0.9 percent ($170 million
decrease). The $80 million in decreased payments is reflected in the
last column of the first row in Table 25 as a 0.4 percent decrease in
expenditures when comparing CY 2017 payments to estimated CY 2018
payments.
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 hospitals and most other providers and
suppliers are small entities, either by nonprofit status or by having
revenues of less than $7.5 million to $38.5 million in any one year.
For the purposes of the RFA, we estimate that almost all HHAs are small
entities as that term is used in the RFA. Individuals and states are
not included in the definition of a small entity. The economic impact
assessment is based on estimated Medicare payments (revenues) and HHS's
practice in interpreting the RFA is to consider effects economically
``significant'' only if greater than 5 percent of providers reach a
threshold of 3 to 5 percent or more of total revenue or total costs.
The majority of HHAs' visits are Medicare-paid visits, and therefore,
the majority of HHAs' revenue consists of Medicare payments. Based on
our analysis, we conclude that the policies in this final rule will
result in an estimated total impact of 3 to 5 percent or more on
Medicare revenue for greater than 5 percent of HHAs. Therefore, the
Secretary has determined that this HH PPS rule will have a significant
economic impact on a substantial number of small entities. Further
detail is presented in Table 25, by HHA type and location.
With regards to options for regulatory relief, the sunset of rural
add-on payments for CY 2018 is statutory and we do not have the
authority to authorize rural add-on payments past December 31, 2017. We
believe it is appropriate to reduce the national, standardized 60-day
episode payment amount by 0.97 percent in CY 2018 to account for the
estimated increase in nominal case-mix in order to move towards more
accurate payment for the delivery of home health services where
payments better align with the costs of providing such services.
2. HHVBP Model
Under the HHVBP Model, the first payment adjustment will apply in
CY 2018 based on PY1 (2016) data and the final payment adjustment will
apply in CY 2022 based on PY5 (2020) data. In the CY 2016 HH PPS final
rule, we estimated that the overall impact of the HHVBP Model from CY
2018 through CY 2022 was a reduction of approximately $380 million (80
FR 68716). In the CY 2017 HH PPS final rule, we estimated that the
overall impact of the HHVBP Model from CY 2018 through CY 2022 was a
reduction
[[Page 51747]]
of approximately $378 million (81 FR 76795). We do not believe the
changes finalized in this final rule will affect the prior estimates.
C. Detailed Economic Analysis
This final rule updates for CY 2018 the HH PPS rates contained in
the CY 2017 HH PPS final rule (81 FR 76702 through 76797). The impact
analysis of this final rule presents the estimated expenditure effects
of policy changes that are be finalized. We use the latest data and
best analysis available, but we do not make adjustments for future
changes in such variables as number of visits or case-mix.
This analysis incorporates the latest estimates of growth in
service use and payments under the Medicare HH benefit, based primarily
on Medicare claims data from 2016. We note that certain events may
combine to limit the scope or accuracy of our impact analysis, because
such an analysis is future-oriented and, thus, susceptible to errors
resulting from other changes in the impact time period assessed. Some
examples of such possible events are newly-legislated general Medicare
program funding changes made by the Congress, or changes specifically
related to HHAs. In addition, changes to the Medicare program may
continue to be made as a result of the Affordable Care Act, or new
statutory provisions. Although these changes may not be specific to the
HH PPS, the nature of the Medicare program is such that the changes may
interact, and the complexity of the interaction of these changes could
make it difficult to predict accurately the full scope of the impact
upon HHAs.
1. HH PPS for CY 2018
Table 25 represents how HHA revenues are likely to be affected by
the policy changes in this final rule for CY 2018. For this analysis,
we used an analytic file with linked CY 2016 OASIS assessments and HH
claims data for dates of service that ended on or before December 31,
2016. The first column of Table 25 classifies HHAs according to a
number of characteristics including provider type, geographic region,
and urban and rural locations. The second column shows the number of
facilities in the impact analysis. The third column shows the payment
effects of the CY 2018 wage index. The fourth column shows the payment
effects of the CY 2018 case-mix weights. The fifth column shows the
effects the 0.97 percent reduction to the national, standardized 60-day
episode payment amount to account for nominal case-mix growth. The
sixth column shows the payment effects from the sunset of the rural
add-on payment provision in statute. The seventh column shows the
effects of the CY 2018 home health payment update percentage.
The last column shows the combined effects of all the policies in
this final rule. Overall, it is projected that aggregate payments in CY
2018 will decrease by 0.4 percent. As illustrated in Table 25, the
combined effects of all of the changes vary by specific types of
providers and by location. We note that some individual HHAs within the
same group may experience different impacts on payments than others due
to the distributional impact of the CY 2018 wage index, the extent to
which HHAs had episodes in case-mix groups where the case-mix weight
decreased for CY 2018 relative to CY 2017, the percentage of total HH
PPS payments that were subject to the low-utilization payment
adjustment (LUPA) or paid as outlier payments, and the degree of
Medicare utilization. In addition, we clarify that there are negative
estimated impacts attributed to the sunset of the rural add-on
provision for HHAs located in urban areas as well as rural areas. This
is due to the fact that HHAs located in urban areas provide services to
patients located in rural areas and payments are based on the location
of the beneficiary.
Table 25--Estimated HHA Impacts by Facility Type and Area of the Country, CY 2018
--------------------------------------------------------------------------------------------------------------------------------------------------------
60-Day
episode
CY 2018 CY 2018 rate Sunset of HH payment
Number of wage index case-mix nominal rural add- update Total %
agencies \1\ % weights \2\ case-mix on percentage
% reduction \4\ %
\3\ %
--------------------------------------------------------------------------------------------------------------------------------------------------------
All Agencies................................................. 11,056 0.0 0.0 -0.9 -0.5 1.0 -0.4
--------------------------------------------------------------------------------------------------------------------------------------------------------
Facility Type and Control
--------------------------------------------------------------------------------------------------------------------------------------------------------
Free-Standing/Other Vol/NP................................... 1,110 0.0 0.1 -0.8 -0.4 1.0 -0.1
Free-Standing/Other Proprietary.............................. 8,724 0.0 0.0 -0.9 -0.4 1.0 -0.3
Free-Standing/Other Government............................... 318 -0.3 0.1 -0.9 -1.3 1.0 -1.4
Facility-Based Vol/NP........................................ 634 0.0 0.2 -0.8 -0.7 1.0 -0.3
Facility-Based Proprietary................................... 81 -0.3 0.2 -0.9 -1.3 1.0 -1.3
Facility-Based Government.................................... 189 0.0 0.2 -0.9 -1.5 1.0 -1.2
Subtotal: Freestanding....................................... 10,152 0.0 0.0 -0.9 -0.4 1.0 -0.3
Subtotal: Facility-based..................................... 904 0.0 0.2 -0.8 -0.8 1.0 -0.4
Subtotal: Vol/NP............................................. 1,744 0.0 0.1 -0.8 -0.5 1.0 -0.2
Subtotal: Proprietary........................................ 8,805 0.0 0.0 -0.9 -0.5 1.0 -0.4
Subtotal: Government......................................... 507 -0.2 0.2 -0.9 -1.4 1.0 -1.3
--------------------------------------------------------------------------------------------------------------------------------------------------------
Facility Type and Control: Rural
--------------------------------------------------------------------------------------------------------------------------------------------------------
Free-Standing/Other Vol/NP................................... 265 0.2 0.1 -0.9 -2.5 1.0 -2.1
Free-Standing/Other Proprietary.............................. 832 -0.1 -0.2 -0.9 -2.3 1.0 -2.5
Free-Standing/Other Government............................... 224 -0.4 0.0 -0.9 -2.6 1.0 -2.9
Facility-Based Vol/NP........................................ 285 -0.4 0.1 -0.8 -2.7 1.0 -2.8
Facility-Based Proprietary................................... 42 -0.1 0.1 -0.9 -2.7 1.0 -2.6
Facility-Based Government.................................... 142 -0.2 0.1 -0.8 -2.6 1.0 -2.5
--------------------------------------------------------------------------------------------------------------------------------------------------------
Facility Type and Control: Urban
--------------------------------------------------------------------------------------------------------------------------------------------------------
Free-Standing/Other Vol/NP................................... 845 -0.9 0.1 -0.8 -0.1 1.0 -0.7
Free-Standing/Other Proprietary.............................. 7,892 0.0 0.0 -0.9 -0.2 1.0 -0.1
Free-Standing/Other Government............................... 94 -0.3 0.2 -0.9 -0.1 1.0 -0.1
Facility-Based Vol/NP........................................ 349 0.1 0.2 -0.8 -0.1 1.0 0.4
Facility-Based Proprietary................................... 39 -0.5 0.2 -0.9 -0.2 1.0 -0.4
[[Page 51748]]
Facility-Based Government.................................... 47 0.3 0.2 -0.9 -0.3 1.0 0.3
--------------------------------------------------------------------------------------------------------------------------------------------------------
Facility Location: Urban or Rural
--------------------------------------------------------------------------------------------------------------------------------------------------------
Rural........................................................ 1,790 -0.1 -0.1 -0.9 -2.4 1.0 -2.5
Urban........................................................ 9,266 0.0 0.0 -0.9 -0.2 1.0 -0.1
--------------------------------------------------------------------------------------------------------------------------------------------------------
Facility Location: Region of the Country (Census Region)
--------------------------------------------------------------------------------------------------------------------------------------------------------
New England.................................................. 359 0.0 0.1 -0.8 -0.3 1.0 0.0
Mid Atlantic................................................. 495 0.0 -0.1 -0.8 -0.2 1.0 -0.1
East North Central........................................... 2,235 0.0 0.2 -0.9 -0.4 1.0 -0.1
West North Central........................................... 711 0.2 0.1 -0.9 -0.8 1.0 -0.4
South Atlantic............................................... 1,736 -0.2 -0.1 -0.9 -0.3 1.0 -0.5
East South Central........................................... 426 -0.2 -0.2 -0.9 -1.3 1.0 -1.6
West South Central........................................... 2,987 0.2 -0.3 -0.9 -0.7 1.0 -0.7
Mountain..................................................... 683 -0.2 0.1 -0.9 -0.4 1.0 -0.4
Pacific...................................................... 1,377 0.1 0.5 -0.9 -0.1 1.0 0.6
Other........................................................ 47 0.1 -1.0 -0.8 -0.6 1.0 -1.3
--------------------------------------------------------------------------------------------------------------------------------------------------------
Facility Size (Number of 1st Episodes)
--------------------------------------------------------------------------------------------------------------------------------------------------------
<100 episodes................................................ 3,092 0.0 0.1 -0.9 -0.4 1.0 -0.2
100 to 249................................................... 2,467 0.1 0.2 -0.9 -0.5 1.0 -0.1
250 to 499................................................... 2,225 0.1 0.2 -0.9 -0.5 1.0 -0.1
500 to 999................................................... 1,710 0.0 0.0 -0.9 -0.5 1.0 -0.4
1,000 or More................................................ 1,562 -0.1 -0.1 -0.9 -0.5 1.0 -0.6
--------------------------------------------------------------------------------------------------------------------------------------------------------
Source: CY 2016 Medicare claims data for episodes ending on or before December 31, 2016 for which we had a linked OASIS assessment.
\1\ The impact of the CY 2018 home health wage index is offset by the wage index budget neutrality factor described in section III.C.3 of this final
rule.
\2\ The impact of the CY 2018 home health case-mix weights reflects the recalibration of the case-mix weights offset by the case-mix weights budget
neutrality factor described in section III.B of this final rule.
\3\ The 0.97 percent reduction to the national, standardized 60-day episode payment amount in CY 2018 is estimated to have a 0.9 percent impact on
overall HH PPS expenditures.
\4\ The CY 2018 home health payment update percentage reflects the home health payment update of 1 percent as described in section III.C.1 of this final
rule.
REGION KEY:
New England = Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont.
Middle Atlantic = Pennsylvania, New Jersey, New York.
South Atlantic = Delaware, District of Columbia, Florida, Georgia, Maryland, North Carolina, South Carolina, Virginia, West Virginia.
East North Central = Illinois, Indiana, Michigan, Ohio, Wisconsin.
East South Central = Alabama, Kentucky, Mississippi, Tennessee.
West North Central = Iowa, Kansas, Minnesota, Missouri, Nebraska, North Dakota, South Dakota.
West South Central = Arkansas, Louisiana, Oklahoma, Texas.
Mountain = Arizona, Colorado, Idaho, Montana, Nevada, New Mexico, Utah, Wyoming.
Pacific = Alaska, California, Hawaii, Oregon, Washington.
Other = Guam, Puerto Rico, Virgin Islands.
The following is a summary of the public comments received on the
``Regulatory Impact Analysis'' and our responses:
Comment: A commenter requested that CMS provide the impact analyses
of the case-mix weight changes that are annually proposed.
Response: The analyses of the annual case-mix weight changes are
included in Table 25 in the fourth column titled, ``CY 2018 Case-Mix
Weights''.
Comment: A commenter stated that when isolating the case mix
changes from CY2017 to the CY2018 proposed rule, they are seeing an
average impact of -0.58% which differs from the CMS projected 0.0
percent in Table 54 of the proposed rule. This analysis is for the
case-mix components only (weights and budget neutrality factor), and
excludes all other components such as wage index, nominal CM reduction,
sunset of rural add-on, and the payment update percentage. The
commenter requested an explanation of the apparent discrepancy.
Response: We estimate that all HHAs nationwide will see a decrease
in average case-mix between CY 2017 and CY 2018 of 1.6 percent due to
recalibration of the case-mix weights (hence the BN factor of 1.6
percent). In increasing the base rate by 1.6 percent to offset the
decrease in average case-mix, those HHAs that have a decrease in
average case-mix of less than 1.6 percent between CY 2017 and CY 2018
will see a small increase in payment for CY 2018 due to the case-mix
weights budget neutrality factor. Those HHAs that have a decrease in
average case-mix of more than 1.6 percent due to the case-mix weight
recalibration between CY 2017 and CY 2018 will see a small decrease in
payment for CY 2018 (generally proportional to the decrease in average
case-mix above and beyond -1.6 percent). The adjustment for case-mix
normalization is budget neutral in the aggregate but not so for
individual HHAs.
2. HHVBP Model
Table 26 displays our analysis of the distribution for possible
payment adjustments at the 3-percent, 5-percent, 6-percent, 7-percent,
and 8-percent rates that are being used in the Model using CY 2015
baseline data and CY 2016 PY 1 data for OASIS-based measures, claims-
based hospitalization and Emergency Department (ED) measures, and
HHCAHPS data. The estimated impacts account for the minimum 40 HHCAHPS
completed surveys policy, beginning with PY 1, as finalized in this
rule. For PY 1 and 2, we show the impacts based on ten OASIS quality
measures (9 OASIS quality measures were used for PY 3 through 5 to
represent the removal of the Drug Education measure), two claims-based
measures in QIES, five HHCAHPS measures, and the three new measures
[[Page 51749]]
(using the October 2016 and January 2017 submission data), using the
QIES Roll Up File data in the same manner as they will be in the Model.
HHAs were classified as being in the smaller or larger volume cohort
using the 2015 Quality Episode File, as updated for this final rule,
which is created using OASIS assessments. The basis of the payment
adjustment was derived from complete 2015 claims data. We note that
this impact analysis is based on the aggregate value of all nine
states.
Table 27 displays our analysis of the distribution of possible
payment adjustments based on the same CY 2015 baseline data and 2016 PY
1 data used to calculate Table 26, providing information on the
estimated impact of the finalized policies in this final rule. Note
that all Medicare-certified HHAs that provide services in
Massachusetts, Maryland, North Carolina, Florida, Washington, Arizona,
Iowa, Nebraska, and Tennessee are required to compete in this Model.
This analysis reflects that only HHAs that have data for at least five
measures that meet the requirements of Sec. 484.305, as amended by
this final rule, will be included in the LEF and will have a payment
adjustment calculated. Value-based incentive payment adjustments for
the estimated 1,600 plus HHAs in the selected states that will compete
in the HHVBP Model are stratified by size as described in section IV.B.
of the CY 2017 HH PPS final rule. As finalized in section IV.B. of the
CY 2017 HH PPS final rule, there must be a minimum of eight HHAs in any
cohort.
Those HHAs that are in states that do not have at least eight
smaller-volume HHAs do not have a separate smaller-volume cohort and
thus there will only be one cohort that will include all the HHAs in
that state. As indicated in Table 27, Arizona, Maryland, North
Carolina, Tennessee and Washington will only have one cohort while
Florida, Iowa, Massachusetts, and Nebraska will have both a smaller-
volume cohort and a larger-volume cohort. For example, Iowa has 26 HHAs
exempt from the requirement that their beneficiaries complete HHCAHPS
surveys because they provided HHA services to fewer than 60
beneficiaries in CY 2015. Therefore, 26 HHAs competed in Iowa's
smaller-volume cohort for the 2016 performance year under the Model.
Using CY 2015 baseline year data and CY 2016 PY 1 data and the
maximum payment adjustment for PY 1 of 3-percent (as applied in CY
2018), based on the ten OASIS quality measures, two claims-based
measures in QIES, the five HHCAHPS measures, and the three new
measures, the smaller-volume HHAs in Iowa have a mean payment
adjustment of -0.1 percent (Table 27). Ten percent of HHAs in the
smaller-volume cohort will be subject to payment adjustments of more
than minus 1.1 percent (-1.1 percent), the lowest 10th percentile. The
next columns provide the distribution of scores by percentile; we see
that the cohort payment adjustment distribution for HHAs in Iowa in the
smaller-volume cohort ranges from -1.1 percent at the 10th percentile
to +1.5 percent at the 90th percentile, while the cohort payment
adjustment distribution median is -0.3 percent.
Table 28 provides the payment adjustment distribution based on
agency size, proportion of dually-eligible beneficiaries, average case
mix (using the average case-mix for non-LUPA episodes), the proportion
of the HHA's beneficiaries that reside in rural areas and HHA
organizational status. HHAs with a higher proportion of dually-eligible
beneficiaries and HHAs whose beneficiaries have higher acuity tend to
have better performance.
The payment adjustment percentages are calculated at the state and
size cohort level. Hence, the values of each separate analysis in the
tables reflect the baseline year of 2015 and the performance year of
2016. There are 1,622 Medicare-certified HHAs in the nine selected
states that have a sufficient number of measures to receive a payment
adjustment in the Model. We note in Table 28, that at the time of our
analysis, seven of the 1,622 Medicare-certified HHAs were missing
information needed for the stratifications in the table. Not all
Medicare-certified HHAs in the nine states have a payment adjustment
because some HHAs are servicing too small of a population to report an
adequate number of measures to calculate a TPS. However, as noted
previously, our updated analysis found that the number of such HHAs was
not affected by the proposed minimum 40 HHCAHPS survey policy, which we
are finalizing.
Additional analysis (see Table 29) was conducted to illustrate the
effect of the finalized policy to require 40 or more completed HHCAHPS
surveys versus 20 or more completed HHCAHPS surveys. We include
information on average statewide TPS by size of the HHA. The percentage
difference in the average TPS across all larger-volume HHAs for each
state ranges from -0.3 percent through 1.8 percent and the majority of
states are close to zero.
Table 26--Adjustment Distribution by Percentile Level of Quality Total Performance Score at Different Model Payment Adjustment Rates
[Percentage]*
--------------------------------------------------------------------------------------------------------------------------------------------------------
Range
Payment adjustment distribution (%) 10% 20% 30% 40% Median 60% 70% 80% 90%
--------------------------------------------------------------------------------------------------------------------------------------------------------
3% Payment Adjustment For Performance Year 1 of the Model..... 2.8 -1.3 -0.9 -0.6 -0.4 -0.1 0.2 0.5 0.8 1.4
5% Payment Adjustment For Performance Year 2 of the Model..... 4.6 -2.2 -1.6 -1.0 -0.6 -0.1 0.3 0.8 1.4 2.4
6% Payment Adjustment For Performance Year 3 of the Model**... 5.8 -2.8 -1.9 -1.3 -0.7 -0.2 0.4 1.0 1.7 3.0
7% Payment Adjustment For Performance Year 4 of the Model**... 6.7 -3.2 -2.2 -1.5 -0.9 -0.2 0.5 1.2 1.9 3.5
8% Payment Adjustment For Performance Year 5 of the Model**... 7.7 -3.7 -2.5 -1.7 -1.0 -0.2 0.5 1.4 2.2 4.0
--------------------------------------------------------------------------------------------------------------------------------------------------------
* Based on measure performance data from Performance Year 1 (January 1, 2016 to December 31, 2016), the baseline year (January 1, 2015 to December 31,
2015), and home health Medicare claims data from 2015.
** For Performance Years 3, 4, and 5, the payment adjustment rate simulation incorporated the removal of the Drug Education measure.
Table 27--HHA Cohort Payment Adjustment Distributions by State/Cohort
[Based on a 3-percent payment adjustment]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average
State Number of payment adj. 10% 20% 30% 40% 50% 60% 70% 80% 90%
HHAs %
--------------------------------------------------------------------------------------------------------------------------------------------------------
HHA Cohort in States with no small cohorts (percent)
--------------------------------------------------------------------------------------------------------------------------------------------------------
AZ......................................... 114 -0.1 -1.3 -0.9 -0.7 -0.4 -0.2 0.1 0.5 0.7 1.1
MD......................................... 51 0.1 -0.8 -0.8 -0.6 -0.4 0.1 0.4 0.5 0.8 1.0
[[Page 51750]]
NC......................................... 163 -0.1 -1.3 -0.9 -0.5 -0.2 0.0 0.2 0.4 0.7 0.9
TN......................................... 123 -0.1 -1.3 -1.0 -0.7 -0.4 -0.1 0.2 0.3 0.6 1.0
WA......................................... 57 -0.1 -1.0 -0.8 -0.6 -0.2 -0.2 0.0 0.3 0.3 0.8
--------------------------------------------------------------------------------------------------------------------------------------------------------
Smaller-volume HHA Cohort in states with small cohort (percent)
--------------------------------------------------------------------------------------------------------------------------------------------------------
FL......................................... 82 0.1 -1.6 -1.3 -1.0 -0.6 -0.2 0.6 0.9 1.5 2.2
IA......................................... 26 -0.1 -1.1 -1.0 -0.9 -0.6 -0.3 0.0 0.4 0.8 1.5
MA......................................... 16 -0.4 -1.7 -1.5 -1.5 -1.1 -0.8 -0.4 0.3 0.8 2.3
NE......................................... 16 0.2 -1.6 -1.5 -1.0 -0.1 0.2 0.6 1.1 1.2 2.7
--------------------------------------------------------------------------------------------------------------------------------------------------------
Large-volume HHA Cohort in states with small cohort (percent)
--------------------------------------------------------------------------------------------------------------------------------------------------------
FL......................................... 706 0.1 -1.2 -0.8 -0.5 -0.3 0.0 0.2 0.6 1.0 1.7
IA......................................... 99 -0.2 -1.4 -1.1 -0.8 -0.5 -0.3 0.0 0.3 0.7 1.2
MA......................................... 124 -0.2 -1.5 -1.1 -0.8 -0.6 -0.3 0.0 0.3 0.6 1.1
NE......................................... 45 0.0 -1.4 -0.7 -0.6 -0.2 0.1 0.3 0.7 0.9 1.2
--------------------------------------------------------------------------------------------------------------------------------------------------------
Notes: Based on measure performance data from Performance Year 1 (January 1, 2016 to December 31, 2016), the baseline year (January 1, 2015 to December
31, 2015), and home health Medicare claims data from 2015.
Table 28--Payment Adjustment Distributions by Characteristics
[Based on a 3-percent payment adjustment]\1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average
Cohort HHAs payment adj. % 10% 20% 30% 40% 50% 60% 70% 80% 90%
--------------------------------------------------------------------------------------------------------------------------------------------------------
Small HHA (<60 patients in CY 2015)........ 150 0.0 -1.6 -1.4 -1.0 -0.6 -0.3 0.2 0.7 1.2 2.2
Large HHA (>=60 patients in CY 2015)....... 1,465 0.0 -1.2 -0.9 -0.6 -0.3 -0.1 0.2 0.5 0.8 1.4
Low % Dually-Eligible...................... 403 0.1 -1.1 -0.8 -0.5 -0.2 0.1 0.3 0.6 0.9 1.4
Medium % Dually-Eligible................... 809 -0.1 -1.3 -0.9 -0.6 -0.4 -0.1 0.1 0.4 0.6 1.0
High % Dually-Eligible..................... 403 0.1 -1.5 -1.1 -0.8 -0.5 -0.1 0.3 0.7 1.3 2.1
Low Acuity................................. 403 -0.3 -1.6 -1.2 -1.0 -0.7 -0.4 -0.1 0.2 0.6 1.1
Mid Acuity................................. 809 0.0 -1.2 -0.9 -0.6 -0.4 -0.1 0.1 0.4 0.7 1.2
High Acuity................................ 403 0.4 -1.1 -0.6 -0.3 0.0 0.3 0.6 0.9 1.4 2.1
All non-rural beneficiaries................ 956 0.1 -1.3 -0.9 -0.6 -0.3 0.0 0.3 0.6 1.0 1.7
Up to 35% rural beneficiaries.............. 384 -0.1 -1.3 -0.9 -0.6 -0.3 -0.1 0.1 0.4 0.7 1.0
Over 35% rural beneficiaries............... 275 -0.1 -1.3 -1.0 -0.7 -0.4 -0.2 0.0 0.2 0.7 1.2
Non-Profit HHAs............................ 295 0.1 -1.1 -0.8 -0.5 -0.2 0.0 0.3 0.6 0.9 1.3
For-Profit HHAs............................ 1,211 0.0 -1.4 -1.0 -0.6 -0.4 -0.1 0.2 0.5 0.8 1.5
Government HHAs............................ 109 -0.2 -1.1 -0.9 -0.8 -0.5 -0.3 0.0 0.1 0.4 1.0
Freestanding............................... 1,460 0.0 -1.3 -0.9 -0.6 -0.4 -0.1 0.2 0.5 0.8 1.5
Facility-based............................. 155 -0.1 -1.3 -0.9 -0.6 -0.3 -0.1 0.1 0.3 0.7 1.0
--------------------------------------------------------------------------------------------------------------------------------------------------------
Notes:
\1\ Rural beneficiaries identified based on the CBSA code reported on the claim. Acuity is based on the average case-mix weight for non-LUPA episodes.
Low acuity is defined as the bottom 25 percent (among HHVBP Model participants); mid-acuity is the middle 50 percent and high acuity is the highest 25
percent. Note that at the time of the analysis, seven HHAs were missing information needed for the stratifications in this table.
Table 29--Impact of Changing Minimum Required Sample Size for HHCAHPS Performance Measures on Average TPS and Payment Adjustment Range*
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average TPS Minimum payment Maximum payment
--------------------------------------------------- adjustment adjustment
-----------------------------------------------
State HHA count % 20 40
20 Minimum 40 Minimum Difference Difference Minimum Minimum 20 Minimum 40 Minimum
(%) (%) (%) (%)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Larger-volume HHAS
--------------------------------------------------------------------------------------------------------------------------------------------------------
AZ........................................ 107 42.160 42.924 0.765 1.8 -2.3 -2.3 2.8 2.7
FL........................................ 706 39.110 39.731 0.621 1.6 -2.5 -2.5 3.0 3.0
IA........................................ 99 43.191 43.186 -0.005 0.0 -2.1 -2.1 2.0 2.4
MA........................................ 124 41.380 41.256 -0.125 -0.3 -2.6 -2.5 2.4 2.5
MD........................................ 50 49.179 49.549 0.370 0.7 -1.3 -1.3 2.0 2.0
NC........................................ 163 45.798 46.187 0.390 0.8 -2.1 -2.1 2.9 2.9
NE........................................ 45 42.252 43.028 0.776 1.8 -2.1 -2.1 2.6 2.4
TN........................................ 119 47.462 47.540 0.078 0.2 -2.5 -2.3 1.6 2.1
WA........................................ 57 51.840 51.712 -0.128 -0.2 -1.5 -1.6 1.1 1.1
-------------------------------------------------------------------------------------------------------------
Total................................. 1,470 ........... ........... ........... .......... ......... ......... ........... ...........
--------------------------------------------------------------------------------------------------------------------------------------------------------
Smaller-volume HHAS
--------------------------------------------------------------------------------------------------------------------------------------------------------
AZ........................................ 7 36.706 36.706 0.000 0.0 -1.8 -1.9 1.0 1.0
FL........................................ 82 42.810 42.810 0.000 0.0 -2.3 -2.3 2.9 2.9
IA........................................ 26 38.663 38.663 0.000 0.0 -1.8 -1.8 2.2 2.2
MA........................................ 16 25.004 25.004 0.000 0.0 -1.7 -1.7 2.3 2.3
[[Page 51751]]
MD........................................ 1 61.135 61.135 0.000 0.0 0.8 0.8 0.8 0.8
NE........................................ 16 37.485 37.485 0.000 0.0 -2.6 -2.6 3.0 3.0
TN........................................ 4 39.983 39.983 0.000 0.0 -1.8 -1.8 1.9 1.9
-------------------------------------------------------------------------------------------------------------
Total................................. 152 ........... ........... ........... .......... ......... ......... ........... ...........
-------------------------------------------------------------------------------------------------------------
Total................................. 1,622 ........... ........... ........... .......... ......... ......... ........... ...........
--------------------------------------------------------------------------------------------------------------------------------------------------------
* OASIS, claims and HHCAHPS measures run from January 1, 2016 to December 31, 2016 for Performance Year 1. The baseline year is January 1, 2015 to
December 31, 2015. Payment based on 2015 Medicare home health claims data. North Carolina and Washington did not have any smaller-volume HHAs.
3. HH QRP
Failure to submit data required under section 1895(b)(3)(B)(v) of
the Act will result in the reduction of the annual update to the
standard federal rate for discharges occurring during such fiscal year
by 2 percentage points for any HHA that does not comply with the
requirements established by the Secretary. At the time that this
analysis was prepared, 1,206, or approximately 9.9 percent, of the
12,149 active Medicare-certified HHAs, did not receive the full annual
percentage increase for CY 2017 because they did not meet the
requirements of the HH QRP. Information is not available to determine
the precise number of HHAs that will not meet the requirements to
receive the full annual percentage increase for the CY 2018 payment
determination.
As noted in section VII.B. of this final rule, the net effect of
our provisions is an estimated decrease in cost associated with changes
to the HH QRP on average of $12,016.33 per HHA annually, or
$145,986,343.50 for all HHAs annually.
Comment: A commenter stated that CMS had underestimated the cost of
changes to the OASIS, adding that CMS had not considered training and
opportunity costs related to data set changes.
Response: Our burden estimates reflect the burden on data
submission. We intend to provide educational resources on the OASIS
changes, including training and guidance, to providers at no cost.
D. Accounting Statements and Tables
As required by OMB Circular A-4 (available at https://www.whitehouse.gov/omb/circulars_a004_a-4), in Table 30, we have
prepared an accounting statement showing the classification of the
transfers and costs associated with the HH PPS provisions of this final
rule. Table 30 provides our best estimate of the decrease in Medicare
payments under the HH PPS as a result of the changes presented in this
final rule for the HH PPS provisions in CY 2018. Table 31 provides our
best estimates of the changes associated with the HH QRP provisions.
Table 30--Accounting Statement: HH PPS Classification of Estimated
Transfers, From CY 2017 To 2018
------------------------------------------------------------------------
Category Transfers
------------------------------------------------------------------------
Annualized Monetized Transfers............ -$80 million.
From Whom to Whom? Federal Government to HHAs.
------------------------------------------------------------------------
Table 31--Accounting Statement: HH QRP Classification of Estimated
Costs, From CY 2018 To 2019
------------------------------------------------------------------------
Category Costs
------------------------------------------------------------------------
Annualized Monetized Net Burden for -$146.0 million.
HHAs Submission of the OASIS.
------------------------------------------------------------------------
E. Reducing Regulation and Controlling Regulatory Costs
Executive Order 13771, entitled Reducing Regulation and Controlling
Regulatory Costs (82 FR 9339), was issued on January 30, 2017. This
final rule is considered an E.O. 13771 deregulatory action. Details on
the estimated cost savings of this proposed rule can be found in the
rule's PRA and economic analysis.
F. Conclusion
1. HH PPS
In conclusion, we estimate that the net impact of the HH PPS
policies in this final rule is a decrease of 0.4 percent, or $80
million, in Medicare payments to HHAs for CY 2018. The -$80 million
impact reflects the effects of a 0.5 percent reduction in payments due
to the sunset of the rural add-on provision ($100 million decrease), a
1 percent CY 2018 HH payment update percentage ($190 million increase),
and a 0.9 percent decrease in payments due to the 0.97 percent
reduction to the national, standardized 60-day episode payment rate in
CY 2017 to account for nominal case-mix growth ($170 million decrease).
2. HHVBP Model
In conclusion, we estimate there will be no net impact (to include
either a net increase or reduction in payments) in this final rule in
Medicare payments to HHAs competing in the HHVBP Model for CY 2018.
However, the overall economic impact of the HHVBP Model is an estimated
$378 million in total savings from a reduction in unnecessary
hospitalizations and SNF usage as a result of greater quality
improvements in the home health industry over the life of the HHVBP
Model.
3. HH QRP
In conclusion, for CY 2019 we estimate that there will be a total
decrease in costs of $145,986,343.50 associated with the changes to the
HH QRP.
This analysis, together with the remainder of this preamble,
provides afinal Regulatory Flexibility Analysis.
[[Page 51752]]
VIII. Federalism Analysis
Executive Order 13132 on Federalism (August 4, 1999) establishes
certain requirements that an agency must meet when it promulgates a
final rule that imposes substantial direct requirement costs on state
and local governments, preempts state law, or otherwise has Federalism
implications. We have reviewed this final rule under the threshold
criteria of Executive Order 13132, Federalism, and have determined that
it will not have substantial direct effects on the rights, roles, and
responsibilities of states, local or tribal governments.
In accordance with the provisions of Executive Order 12866, this
final rule was reviewed by the Office of Management and Budget.
List of Subjects for 42 CFR Part 484
Health facilities, Health professions, Medicare, Reporting and
recordkeeping requirements.
For the reasons set forth in the preamble, the Centers for Medicare
& Medicaid Services amends 42 CFR part 484 as set forth below:
PART 484--HOME HEALTH SERVICES
0
1. The authority citation for part 484 continues to read as follows:
Authority: Secs 1102 and 1871 of the Act (42 U.S.C. 1302 and
1395(hh)) unless otherwise indicated.
0
2. Section 484.250 is amended by revising paragraph (a)(1) and adding
paragraphs (d) through (f) to read as follows:
Sec. 484.250 Patient assessment data.
(a) * * *
(1) The OASIS data described at Sec. 484.55(b) and (d) for CMS to
administer the payment rate methodologies described in Sec. Sec.
484.215, 484.220, 484. 230, 484.235, and 484.240; and to meet the
quality reporting requirements of section 1895(b)(3)(B)(v) of the Act.
* * * * *
(d) Exceptions and extension requirements. (1) A HHA may request
and CMS may grant exceptions or extensions to the reporting
requirements under section 1895(b)(3)(B)(v) of the Act for one or more
quarters, when there are certain extraordinary circumstances beyond the
control of the HHA.
(2) A HHA may request an exception or extension within 90 days of
the date that the extraordinary circumstances occurred by sending an
email to CMS HHAPU reconsiderations at
HHAPUReconsiderations@cms.hhs.gov that contains all of the following
information:
(i) HHA CMS Certification Number (CCN).
(ii) HHA Business Name.
(iii) HHA Business Address.
(iv) CEO or CEO-designated personnel contact information including
name, telephone number, title, email address, and mailing address (the
address must be a physical address, not a post office box).
(v) HHA's reason for requesting the exception or extension.
(vi) Evidence of the impact of extraordinary circumstances,
including, but not limited to, photographs, newspaper, and other media
articles.
(vii) Date when the HHA believes it will be able to again submit
data under section 1895(b)(3)(B)(v) of the Act and a justification for
the proposed date.
(3) Except as provided in paragraph (d)(4) of this section, CMS
will not consider an exception or extension request unless the HHA
requesting such exception or extension has complied fully with the
requirements in this paragraph (d).
(4) CMS may grant exceptions or extensions to HHAs without a
request if it determines that one or more of the following has
occurred:
(i) An extraordinary circumstance affects an entire region or
locale.
(ii) A systemic problem with one of CMS's data collection systems
directly affected the ability of a HHA to submit data under section
1895(b)(3)(B)(v) of the Act.
(e) Reconsideration. (1) HHAs that do not meet the quality
reporting requirements under section 1895(b)(3)(B)(v) of the Act for a
program year will receive a letter of non-compliance via the United
States Postal Service and notification in CASPER. An HHA may request
reconsideration no later than 30 calendar days after the date
identified on the letter of non-compliance.
(2) Reconsideration requests may be submitted to CMS by sending an
email to CMS HHAPU reconsiderations at
HHAPureConsiderations@cms.hhs.gov containing all of the following
information:
(i) HHA CCN.
(ii) HHA Business Name.
(iii) HHA Business Address.
(iv) CEO or CEO-designated personnel contact information including
name, telephone number, title, email address, and mailing address (the
address must be a physical address, not a post office box).
(v) CMS identified reason(s) for non-compliance from the non-
compliance letter.
(vi) Reason(s) for requesting reconsideration, including all
supporting documentation.
(3) CMS will not consider an exception or extension request unless
the HHA has complied fully with the requirements in paragraph (e)(2) of
this section.
(4) CMS will make a decision on the request for reconsideration and
provide notice of the decision to the HHA through CASPER and via letter
sent via the United States Postal Service.
(f) Appeals. (1) A HHA that is dissatisfied with CMS' decision on a
request for reconsideration submitted under paragraph (e) of this
section may file an appeal with the Provider Reimbursement Review Board
(PRRB) under 42 CFR part 405, subpart R.
(2) [Reserved]
0
3. Section 484.305 is amended by revising the definition of
``Applicable measure'' to read as follows:
Sec. 484.305 Definitions.
* * * * *
Applicable measure means a measure for which a competing HHA has
provided a minimum of--
(1) Twenty home health episodes of care per year for the OASIS-
based measures;
(2) Twenty home health episodes of care per year for the claims-
based measures; or
(3) Forty completed surveys for the HHCAHPS measures.
* * * * *
Dated: October 23, 2017.
Seema Verma,
Administrator, Centers for Medicare & Medicaid Services.
Dated: October 24, 2017.
Eric D. Hargan,
Acting Secretary, Department of Health and Human Services.
[FR Doc. 2017-23935 Filed 11-1-17; 4:15 pm]
BILLING CODE 4120-01-P