Medicare Program; Inpatient Rehabilitation Facility Prospective Payment System for Federal Fiscal Year 2010, 39762-39838 [E9-18616]
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Federal Register / Vol. 74, No. 151 / Friday, August 7, 2009 / Rules and Regulations
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 412
[CMS–1538–F]
RIN 0938–AP56
Medicare Program; Inpatient
Rehabilitation Facility Prospective
Payment System for Federal Fiscal
Year 2010
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AGENCY: Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Final rule.
SUMMARY: This final rule updates the
payment rates for inpatient
rehabilitation facilities (IRFs) for
Federal fiscal year (FY) 2010 (for
discharges occurring on or after October
1, 2009 and on or before September 30,
2010) as required under section
1886(j)(3)(C) of the Social Security Act
(the Act). Section 1886(j)(5) of the Act
requires the Secretary to publish in the
Federal Register on or before the August
1 that precedes the start of each fiscal
year, the classification and weighting
factors for the IRF prospective payment
system’s (PPS) case-mix groups and a
description of the methodology and data
used in computing the prospective
payment rates for that fiscal year.
We are revising existing policies
regarding the IRF PPS within the
authority granted under section 1886(j)
of the Act.
DATES: Effective Date. The provisions of
the final rule are effective October 1,
2009, except for the amendments to
§ 412.23, § 412.29, and § 412.622 which
are effective January 1, 2010.
Applicability Date. The amendments
to § 412.23, § 412.29, and § 412.622 are
applicable to IRF discharges occurring
on or after January 1, 2010. The updated
IRF prospective payment rates are
applicable for IRF discharges occurring
on or after October 1, 2009 and on or
before September 30, 2010 (FY 2010).
FOR FURTHER INFORMATION CONTACT:
Susanne Seagrave, (410) 786–0044, for
information regarding the payment
policies.
Julie Stankivic, (410) 786–5725, for
general information regarding the
proposed rule.
Jeanette Kranacs, (410) 786–9385, for
information regarding the wage index.
SUPPLEMENTARY INFORMATION:
Table of Contents
I. Background
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A. Historical Overview of the Inpatient
Rehabilitation Facility Prospective
Payment System (IRF PPS)
B. Operational Overview of the Current IRF
PPS
II. Summary of Provisions of the Proposed
Rule
A. Proposed Updates to the IRF PPS for
Federal Fiscal Year (FY) 2010
B. Proposed Revisions to Existing
Regulation Text
C. Proposed New Regulation Text
D. Proposed Rescission of Outdated
HCFAR–85–2–1
III. Analysis of and Responses to Public
Comments
IV. Update to the Case-Mix Group (CMG)
Relative Weights and Average Length of
Stay Values for FY 2010
V. Updates to the Facility-Level Adjustment
Factors for FY 2010
A. Updates to the Adjustment Factors for
FY 2010
B. Budget Neutrality Methodology for the
Updates to the IRF Facility-Level
Adjustment Factors
VI. FY 2010 IRF PPS Federal Prospective
Payment Rates
A. Market Basket Increase Factor and
Labor-Related Share for FY 2010
B. Area Wage Adjustment
C. Description of the Final IRF Standard
Payment Conversion Factor and Payment
Rates for FY 2010
D. Example of the Methodology for
Adjusting the Federal Prospective
Payment Rates
VII. Update to Payments for High-Cost
Outliers Under the IRF PPS
A. Update to the Outlier Threshold
Amount for FY 2010
B. Update to the IRF Cost-to-Charge Ratio
Ceilings
VIII. Inpatient Rehabilitation Facility (IRF)
Coverage Requirements
A. Requirements for the Preadmission
Screening
B. Requirement for a Post-Admission
Physician Evaluation
C. Requirement for an Individualized
Overall Plan of Care
D. Requirements for Evaluating the
Appropriateness of an IRF Admission
E. Requirements for the Interdisciplinary
Team Meetings
F. Requirement for Physician Supervision
G. Requirement Regarding Initiation of
Therapy Services
H. Provision of Group Therapies in IRFs
I. Clarifying and Conforming Amendments
J. HCFAR 85–2 Ruling
IX. Revisions to the Regulation Text To
Require IRFs To Submit Patient
Assessments on Medicare Advantage
Patients for Use in the ‘‘60 Percent Rule’’
Calculations
A. Background on the ‘‘60 Percent Rule’’
Calculations
B. Requirement To Submit Assessment
Data on Medicare Advantage Patients
X. Miscellaneous Comments
XI. Provisions of the Final Rule
A. Payment Provision Changes
B. Regulatory Text Changes
XII. Collection of Information Requirements
XIII. Regulatory Impact Analysis
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A. Overall Impact
B. Anticipated Effects of the Final Rule
C. Alternatives Considered
D. Accounting Statement
E. Conclusion
Regulation Text
Addendum
Acronyms
Because of the many terms to which
we refer by acronym in this final rule,
we are listing the acronyms used and
their corresponding terms in
alphabetical order below.
ADC Average Daily Census
ASCA Administrative Simplification
Compliance Act, Public Law 107–105
BBA Balanced Budget Act of 1997, Public
Law 105–33
BBRA Medicare, Medicaid, and SCHIP
[State Children’s Health Insurance
Program] Balanced Budget Refinement Act
of 1999, Public Law 106–113
BIPA Medicare, Medicaid, and SCHIP [State
Children’s Health Insurance Program]
Benefits Improvement and Protection Act
of 2000, Public Law 106–554
CBSA Core-Based Statistical Area
CCR Cost-to-Charge Ratio
CFR Code of Federal Regulations
CMG Case-Mix Group
DRG Diagnostic Related Group
DSH Disproportionate Share Hospital
FI Fiscal Intermediary
FR Federal Register
FTE Full-time Equivalent
FY Federal Fiscal Year
HCFA Health Care Financing
Administration
HHH Hubert H. Humphrey Building
HIPAA Health Insurance Portability and
Accountability Act, Public Law 104–191
IOM Internet Only Manual
IPF Inpatient Psychiatric Facility
IPPS Inpatient Prospective Payment System
IRF Inpatient Rehabilitation Facility
IRF–PAI Inpatient Rehabilitation Facility—
Patient Assessment Instrument
IRF PPS Inpatient Rehabilitation Facility
Prospective Payment System
IRVEN Inpatient Rehabilitation Validation
and Entry
LTCH Long Term Care Hospital
LIP Low-Income Percentage
MA Medicare Advantage
MAC Medicare Administrative Contractor
MBPM Medicare Benefit Policy Manual
MMSEA Medicare, Medicaid, and SCHIP
Extension Act of 2007, Public Law 110–173
OMB Office of Management and Budget
PAI Patient Assessment Instrument
PPS Prospective Payment System
QIC Qualified Independent Contractors
RAC Recovery Audit Contractors
RAND RAND Corporation
RFA Regulatory Flexibility Act, Public Law
96–354
RIA Regulatory Impact Analysis
RIC Rehabilitation Impairment Category
RPL Rehabilitation, Psychiatric, and LongTerm Care Hospital Market Basket
SCHIP State Children’s Health Insurance
Program
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I. Background
A. Historical Overview of the Inpatient
Rehabilitation Facility Prospective
Payment System (IRF PPS)
Section 4421 of the Balanced Budget
Act of 1997 (BBA), Public Law 105–33,
as amended by section 125 of the
Medicare, Medicaid, and SCHIP (State
Children’s Health Insurance Program)
Balanced Budget Refinement Act of
1999 (BBRA), Public Law 106–113, and
by section 305 of the Medicare,
Medicaid, and SCHIP Benefits
Improvement and Protection Act of
2000 (BIPA), Public Law 106–554,
provides for the implementation of a per
discharge prospective payment system
(PPS) under section 1886(j) of the Social
Security Act (the Act) for inpatient
rehabilitation hospitals and inpatient
rehabilitation units of a hospital
(hereinafter referred to as IRFs).
Payments under the IRF PPS
encompass inpatient operating and
capital costs of furnishing covered
rehabilitation services (that is, routine,
ancillary, and capital costs) but not
direct graduate medical education costs,
costs of approved nursing and allied
health education activities, bad debts,
and other services or items outside the
scope of the IRF PPS. Although a
complete discussion of the IRF PPS
provisions appears in the original FY
2002 IRF PPS final rule (66 FR 41316)
and the FY 2006 IRF PPS final rule (70
FR 47880), we are providing below a
general description of the IRF PPS for
fiscal years (FYs) 2002 through 2009.
Under the IRF PPS from FY 2002
through FY 2005, as described in the FY
2002 IRF PPS final rule (66 FR 41316),
the Federal prospective payment rates
were computed across 100 distinct casemix groups (CMGs). We constructed 95
CMGs using rehabilitation impairment
categories (RICs), functional status (both
motor and cognitive), and age (in some
cases, cognitive status and age may not
be a factor in defining a CMG). In
addition, we constructed five special
CMGs to account for very short stays
and for patients who expire in the IRF.
For each of the CMGs, we developed
relative weighting factors to account for
a patient’s clinical characteristics and
expected resource needs. Thus, the
weighting factors accounted for the
relative difference in resource use across
all CMGs. Within each CMG, we created
tiers based on the estimated effects that
certain comorbidities would have on
resource use.
We established the Federal PPS rates
using a standardized payment
conversion factor (formerly referred to
as the budget neutral conversion factor).
For a detailed discussion of the budget
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neutral conversion factor, please refer to
our FY 2004 IRF PPS final rule (68 FR
45684 through 45685). In the FY 2006
IRF PPS final rule (70 FR 47880), we
discussed in detail the methodology for
determining the standard payment
conversion factor.
We applied the relative weighting
factors to the standard payment
conversion factor to compute the
unadjusted Federal prospective
payment rates under the IRF PPS from
FYs 2002 through 2005. Within the
structure of the payment system, we
then made adjustments to account for
interrupted stays, transfers, short stays,
and deaths. Finally, we applied the
applicable adjustments to account for
geographic variations in wages (wage
index), the percentage of low-income
patients, location in a rural area (if
applicable), and outlier payments (if
applicable) to the IRF’s unadjusted
Federal prospective payment rates.
For cost reporting periods that began
on or after January 1, 2002 and before
October 1, 2002, we determined the
final prospective payment amounts
using the transition methodology
prescribed in section 1886(j)(1) of the
Act. Under this provision, IRFs
transitioning into the PPS were paid a
blend of the Federal IRF PPS rate and
the payment that the IRF would have
received had the IRF PPS not been
implemented. This provision also
allowed IRFs to elect to bypass this
blended payment and immediately be
paid 100 percent of the Federal IRF PPS
rate. The transition methodology
expired as of cost reporting periods
beginning on or after October 1, 2002
(FY 2003), and payments for all IRFs
now consist of 100 percent of the
Federal IRF PPS rate.
We established a CMS Web site as a
primary information resource for the
IRF PPS. The Web site URL is https://
www.cms.hhs.gov/
InpatientRehabFacPPS/ and may be
accessed to download or view
publications, software, data
specifications, educational materials,
and other information pertinent to the
IRF PPS.
Section 1886(j) of the Act confers
broad statutory authority upon the
Secretary to propose refinements to the
IRF PPS. In the FY 2006 IRF PPS final
rule (70 FR 47880) and in correcting
amendments to the FY 2006 IRF PPS
final rule (70 FR 57166) that we
published on September 30, 2005, we
finalized a number of refinements to the
IRF PPS case-mix classification system
(the CMGs and the corresponding
relative weights) and the case-level and
facility-level adjustments. These
refinements included the adoption of
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OMB’s Core-Based Statistical Area
(CBSA) market definitions,
modifications to the CMGs, tier
comorbidities, and CMG relative
weights, implementation of a new
teaching status adjustment for IRFs,
revision and rebasing of the IRF market
basket, and updates to the rural, lowincome percentage (LIP), and high-cost
outlier adjustments. Any reference to
the FY 2006 IRF PPS final rule in this
proposed rule also includes the
provisions effective in the correcting
amendments. For a detailed discussion
of the final key policy changes for FY
2006, please refer to the FY 2006 IRF
PPS final rule (70 FR 47880 and 70 FR
57166).
In the FY 2007 IRF PPS final rule (71
FR 48354), we further refined the IRF
PPS case-mix classification system (the
CMG relative weights) and the caselevel adjustments, to ensure that IRF
PPS payments would continue to reflect
as accurately as possible the costs of
care. For a detailed discussion of the FY
2007 policy revisions, please refer to the
FY 2007 IRF PPS final rule (71 FR
48354).
In the FY 2008 IRF PPS final rule (72
FR 44284), we updated the Federal
prospective payment rates and the
outlier threshold, revised the IRF wage
index policy, and clarified how we
determine high-cost outlier payments
for transfer cases. For more information
on the policy changes implemented for
FY 2008, please refer to the FY 2008 IRF
PPS final rule (72 FR 44284), in which
we published the final FY 2008 IRF
Federal prospective payment rates.
After publication of the FY 2008 IRF
PPS final rule (72 FR 44284), section
115 of the Medicare, Medicaid, and
SCHIP Extension Act of 2007, Public
Law 110–173 (MMSEA), amended
section 1886(j)(3)(C) of the Act to apply
a zero percent increase factor for FYs
2008 and 2009, effective for IRF
discharges occurring on or after April 1,
2008. Section 1886(j)(3)(C) of the Act
requires the Secretary to develop an
increase factor to update the IRF Federal
prospective payment rates for each FY.
Based on the legislative change to the
increase factor, we revised the FY 2008
Federal prospective payment rates for
IRF discharges occurring on or after
April 1, 2008. Thus, the final FY 2008
IRF Federal prospective payment rates
that were published in the FY 2008 IRF
PPS final rule (72 FR 44284) were
effective for discharges occurring on or
after October 1, 2007 and on or before
March 31, 2008; and the revised FY
2008 IRF Federal prospective payment
rates were effective for discharges
occurring on or after April 1, 2008 and
on or before September 30, 2008. The
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revised FY 2008 Federal prospective
payment rates are available on the CMS
Web site at https://www.cms.hhs.gov/
InpatientRehabFacPPS/
07_DataFiles.asp#TopOfPage.
In the FY 2009 IRF PPS final rule (73
FR 46370), we updated the CMG relative
weights, the average length of stay
values, and the outlier threshold;
clarified IRF wage index policies
regarding the treatment of ‘‘New
England deemed’’ counties and multicampus hospitals; and revised the
regulation text in response to section
115 of the MMSEA to set the IRF
compliance percentage at 60 percent
(‘‘the 60 percent rule’’) and continue the
practice of including comorbidities in
the calculation of compliance
percentages. We also applied a zero
percent increase factor for FY 2009. For
more information on the policy changes
implemented for FY 2009, please refer
to the FY 2009 IRF PPS final rule (73 FR
46370), in which we published the final
FY 2009 IRF Federal prospective
payment rates.
B. Operational Overview of the Current
IRF PPS
As described in the FY 2002 IRF PPS
final rule, upon the admission and
discharge of a Medicare Part A fee-forservice patient, the IRF is required to
complete the appropriate sections of a
patient assessment instrument (PAI), the
Inpatient Rehabilitation Facility-Patient
Assessment Instrument (IRF–PAI). All
required data must be electronically
encoded into the IRF–PAI software
product. Generally, the software product
includes patient classification
programming called the GROUPER
software. The GROUPER software uses
specific IRF–PAI data elements to
classify (or group) patients into distinct
CMGs and account for the existence of
any relevant comorbidities.
The GROUPER software produces a
five-digit CMG number. The first digit is
an alpha-character that indicates the
comorbidity tier. The last four digits
represent the distinct CMG number.
Free downloads of the Inpatient
Rehabilitation Validation and Entry
(IRVEN) software product, including the
GROUPER software, are available on the
CMS Web site at https://
www.cms.hhs.gov/
InpatientRehabFacPPS/
06_Software.asp.
Once a patient is discharged, the IRF
submits a Medicare claim as a Health
Insurance Portability and
Accountability Act (HIPAA), Public Law
104–191, compliant electronic claim or,
if the Administrative Simplification
Compliance Act (ASCA), Public Law
107–105, permits, a paper claim (a UB–
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04 or a CMS–1450 as appropriate) using
the five-digit CMG number and sends it
to the appropriate Medicare fiscal
intermediary (FI) or Medicare
Administrative Contractor (MAC).
Claims submitted to Medicare must
comply with both ASCA and HIPAA.
Section 3 of the ASCA amends section
1862(a) of the Act by adding paragraph
(22) which requires the Medicare
program, subject to section 1862(h) of
the Act, to deny payment under Part A
or Part B for any expenses for items or
services ‘‘for which a claim is submitted
other than in an electronic form
specified by the Secretary.’’ Section
1862(h) of the Act, in turn, provides that
the Secretary shall waive such denial in
situations in which there is no method
available for the submission of claims in
an electronic form or the entity
submitting the claim is a small provider.
In addition, the Secretary also has the
authority to waive such denial ‘‘in such
unusual cases as the Secretary finds
appropriate.’’ For more information we
refer the reader to the final rule,
‘‘Medicare Program; Electronic
Submission of Medicare Claims’’ (70 FR
71008, November 25, 2005). CMS
instructions for the limited number of
Medicare claims submitted on paper are
available at: https://www.cms.hhs.gov/
manuals/downloads/clm104c25.pdf.
Section 3 of the ASCA operates in the
context of the administrative
simplification provisions of HIPAA,
which include, among others, the
requirements for transaction standards
and code sets codified in 45 CFR parts
160 and 162, subparts A and I through
R (generally known as the Transactions
Rule). The Transactions Rule requires
covered entities, including covered
healthcare providers, to conduct
covered electronic transactions
according to the applicable transaction
standards. (See the program claim
memoranda issued and published by
CMS at: https://www.cms.hhs.gov/
ElectronicBillingEDITrans/ and listed in
the addenda to the Medicare
Intermediary Manual, Part 3, section
3600).
The Medicare FI or MAC processes
the claim through its software system.
This software system includes pricing
programming called the ‘‘PRICER’’
software. The PRICER software uses the
CMG number, along with other specific
claim data elements and providerspecific data, to adjust the IRF’s
prospective payment for interrupted
stays, transfers, short stays, and deaths,
and then applies the applicable
adjustments to account for the IRF’s
wage index, percentage of low-income
patients, rural location, and outlier
payments. For discharges occurring on
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or after October 1, 2005, the IRF PPS
payment also reflects the new teaching
status adjustment that became effective
as of FY 2006, as discussed in the FY
2006 IRF PPS final rule (70 FR 47880).
II. Summary of Provisions of the
Proposed Rule
As discussed in the FY 2010 IRF PPS
proposed rule (74 FR 21052), we
proposed updates to the IRF PPS,
revisions to existing regulations text for
the purpose of providing greater clarity,
new regulations text to improve
calculation of compliance with the ‘‘60
percent’’ rule, and rescission of an
outdated Health Care Financing
Administration (HFCA) Ruling (HCFAR
85–2–1). These proposals are as follows:
A. Proposed Updates to the IRF PPS for
Federal Fiscal Year (FY) 2010
• Update the FY 2010 IRF PPS
relative weights and average length of
stay values using the most current and
complete Medicare claims and cost
report data in a budget neutral manner,
as discussed in section III of the FY
2010 IRF PPS proposed rule (74 FR
21052, 21055 through 21059).
• Update the FY 2010 IRF facilitylevel adjustments (rural, LIP, and
teaching status adjustments) using the
most current and complete Medicare
claims and cost report data in a budget
neutral manner, as discussed in section
IV of the FY 2010 IRF PPS proposed
rule (74 FR 21052, 21059 through
21062).
• Update the FY 2010 IRF PPS
payment rates by the proposed market
basket, as discussed in section V.A of
the FY 2010 IRF PPS proposed rule (74
FR 21052 at 21062).
• Update the FY 2010 IRF PPS
payment rates by the proposed wage
index and the labor-related share in a
budget neutral manner, as discussed in
section V.A and V.B of the FY 2010 IRF
PPS proposed rule (74 FR 21052, 21062
through 21063).
• Update the outlier threshold
amount for FY 2010, as discussed in
section VI.A of the FY 2010 IRF PPS
proposed rule (74 FR 21052 at 21066).
B. Proposed Revisions to Existing
Regulation Text
• Relocate and revise the criteria for
admission to an inpatient rehabilitation
hospital found at existing § 412.23(b)(3)
through (b)(7) that describe
requirements relating to preadmission
screening, close medical supervision, a
director of rehabilitation, the plan of
care, and a coordinated
multidisciplinary team approach.
Redesignate paragraphs (b)(8) and (b)(9)
of § 412.23 as paragraphs (b)(3) and
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(b)(4) and revise newly redesignated
paragraph (b)(4), as described in section
VII of the FY 2010 IRF PPS proposed
rule (74 FR 21052, 21067 through
21071).
• Revise the section heading at
§ 412.29 to include inpatient
rehabilitation hospitals, as described in
section VII of the FY 2010 IRF PPS
proposed rule (74 FR 21052, 21067
through 21071).
• Relocate and revise the existing
requirements at § 412.29(b) through (f)
that describe the admission
requirements relating to preadmission
screening, close medical supervision, a
director of rehabilitation, the plan of
care, and a coordinated
multidisciplinary team approach, as
described in section VII of the FY 2010
IRF PPS proposed rule (74 FR 21052,
21067 through 21071).
• Revise the section heading at
§ 412.30, as described in section VII of
the FY 2010 IRF PPS proposed rule (74
FR 21052, 21067 through 21071).
• Revise the regulation text in
§ 412.604, § 412.606, § 412.610.
§ 412.614 and § 412.618 to require the
collection of inpatient rehabilitation
facility patient assessment instrument
data on Medicare Part C (Medicare
Advantage) patients in IRFs for use in
the 60 percent rule compliance
percentage calculations, as described in
section VIII of the FY 2010 IRF PPS
proposed rule (74 FR 21052, 21071
through 21073).
• Remove § 412.614(a)(3) that
provides for an exception in the
transmission of IRF–PAI data to CMS, as
described in section VIII of the FY 2010
IRF PPS proposed rule (74 FR 21052,
21071 through 21073).
• Revise the heading at § 412.614(d)
to ‘‘Consequences of failure to submit
complete and timely IRF–PAI data, as
required under paragraph (c) of this
section,’’ as described in section VIII of
the FY 2010 IRF PPS proposed rule (74
FR 21052, 21071 through 21073).
• Revise the heading at
§ 412.614(d)(1) to ‘‘Medicare Part A feefor-service data,’’ as described in section
VIII of the FY 2010 IRF PPS proposed
rule (74 FR 21052, 21071 through
21073).
• Make a technical correction to the
paragraph formerly designated as
§ 412.614(d)(1) and assign the revised
language to a new paragraph
§ 412.614(d)(1)(a), as described in
section VIII of the FY 2010 IRF PPS
proposed rule (74 FR 21052, 21071
through 21073).
• Redesignate paragraph
§ 412.614(d)(2) as § 412.614(d)(1)(b), as
described in section VIII of the FY 2010
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IRF PPS proposed rule (74 FR 21052,
21071 through 21073).
C. Proposed New Regulation Text
• Revise § 412.29, as described in
section VII of the FY 2010 IRF PPS
proposed rule (74 FR 21052, 21067
through 21071), to include the
requirements for admission to an IRF.
• Add a new introductory paragraph
at § 412.30 that includes the
requirements previously found in
§ 412.29(a) (describing the admission
requirements for new and converted
rehabilitation units), as described in
section VII of the FY 2010 IRF PPS
proposed rule (74 FR 21052, 21067
through 21071).
• Revise § 412.610(f) to require that
the IRF provide a copy of the electronic
computer file format of the IRF–PAI to
the contractor upon request, as
described in section VII of the FY 2010
IRF PPS proposed rule (74 FR 21052,
21067 through 21071).
• Add a new paragraph
§ 412.614(d)(2) to indicate that failure of
an IRF to submit IRF–PAI data on all of
its Medicare Part C (Medicare
Advantage) patients will result in
forfeiture of the IRF’s ability to have any
of its Medicare Part C (Medicare
Advantage) data used in the compliance
calculations, as described in section VIII
of the FY 2010 IRF PPS proposed rule
(74 FR 21052, 21071 through 21073).
D. Proposed Rescission of Outdated
HCFAR–85–2–1
Rescind HCFA Ruling 85–2–1 entitled
‘‘Medicare Criteria for Medicare
Coverage of Inpatient Hospital
Rehabilitation Services’’ and set forth
new coverage guidance to implement
the new regulations adopted under this
final rule, as described in section VII of
the FY 2010 IRF PPS proposed rule (74
FR 21052 at 21071).
III. Analysis of and Responses to Public
Comments
We received approximately 686
timely responses, many of which
contained multiple comments on the FY
2010 IRF PPS proposed rule (74 FR
21052) from the public. We received
comments from various trade
associations, inpatient rehabilitation
facilities, individual physicians,
therapists, clinicians, health care
industry organizations, and health care
consulting firms. The following section,
arranged by subject area, includes a
summary of the public comments that
we received, and our responses.
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IV. Update to the Case-Mix Group
(CMG) Relative Weights and Average
Length of Stay Values for FY 2010
As specified in 42 CFR 412.620(b)(1),
we calculate a relative weight for each
CMG that is proportional to the
resources needed by an average
inpatient rehabilitation case in that
CMG. For example, cases in a CMG with
a relative weight of 2, on average, will
cost twice as much as cases in a CMG
with a relative weight of 1. Relative
weights account for the variance in cost
per discharge due to the variance in
resource utilization among the payment
groups, and their use helps to ensure
that IRF PPS payments support
beneficiary access to care as well as
provider efficiency.
In the FY 2010 IRF PPS proposed rule
(74 FR 21052, 21055 through 21059), we
proposed to update the CMG relative
weights and average length of stay
values for FY 2010 using the most
recent available data (at that time, FY
2007 IRF claims and cost report data) to
ensure that IRF PPS payments fully
reflect recent changes in IRF utilization
due to the 60 percent rule and medical
review activities. To ensure that IRF
PPS payments continue to reflect as
accurately as possible the current costs
of care in IRFs, we are updating the
CMG relative weights and average
length of stay values for FY 2010 in this
final rule using FY 2008 IRF claims and
FY 2007 IRF cost report data. These data
are the most current and complete data
available at this time. At this time, only
about 20 percent of the FY 2008 IRF cost
report data are available for analysis, but
the majority of the FY 2008 IRF claims
data are available for analysis.
We have used the same methodology
that we used to update the CMG relative
weights and average length of stay
values in the FY 2009 IRF PPS final rule
(73 FR 46370). In calculating the CMG
relative weights, we use a hospitalspecific relative value method to
estimate operating (routine and
ancillary services) and capital costs of
IRFs. The process used to calculate the
CMG relative weights for this final rule
follows below:
Step 1. We calculate the CMG relative
weights by estimating the effects that
comorbidities have on costs.
Step 2. We adjust the cost of each
Medicare discharge (case) to reflect the
effects found in the first step.
Step 3. We use the adjusted costs from
the second step to calculate CMG
relative weights, using the hospitalspecific relative value method.
Step 4. We normalize the FY 2010
CMG relative weights to the same
average CMG relative weight from the
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CMG relative weights implemented in
the FY 2009 IRF PPS final rule (73 FR
46370).
Consistent with the way we
implemented changes to the IRF
classification system in the FY 2006 IRF
PPS final rule (70 FR 47880 and 70 FR
57166), the FY 2007 IRF PPS final rule
(71 FR 48354), and the FY 2009 IRF PPS
final rule (73 FR 46370), we are revising
the CMG relative weights for FY 2010 in
such a way that total estimated
aggregate payments to IRFs for FY 2010
are estimated to be the same with or
without the changes (that is, in a budget
neutral manner) by applying a budget
neutrality factor to the standard
payment amount. To calculate the
appropriate budget neutrality factor for
use in updating the FY 2010 CMG
relative weights, we use the following
steps:
Step 1. Calculate the estimated total
amount of IRF PPS payments for FY
2010 (with no changes to the CMG
relative weights).
Step 2. Apply the changes to the CMG
relative weights (as discussed above) to
calculate the estimated total amount of
IRF PPS payments for FY 2010.
Step 3. Divide the amount calculated
in step 1 by the amount calculated in
step 2 to determine the budget
neutrality factor (1.0020) that maintains
the same total estimated aggregate
payments in FY 2010 with and without
the changes to the CMG relative
weights.
Step 4. Apply the budget neutrality
factor (1.0020) to the FY 2009 IRF PPS
standard payment amount after the
application of the budget-neutral wage
adjustment factor.
In section VI.C of this final rule, we
discuss the methodology for calculating
the standard payment conversion factor
for FY 2010.
Note that the budget neutrality factor
that we use to update the CMG relative
weights for FY 2010 changed from
1.0004 in the proposed rule to 1.0020 in
this final rule due to the use of updated
FY 2008 IRF claims data in this final
rule.
We received 7 comments on the
proposed updates to the CMG relative
weights and average length of stay
values, which are summarized below.
Comment: The vast majority of
commenters supported the proposed
update to the CMG relative weights and
average length of stay values. However,
most suggested that CMS use FY 2008
IRF claims and cost report data in
updating the CMG relative weights and
average length of stay values for the
final rule, saying that the effects of
recent changes in the 60 percent rule
and the IRF medical necessity review
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activities are continuing to be realized
through FY 2008 and early FY 2009.
Several commenters said that we should
continue to update the CMG relative
weights and average length of stay
values annually to reflect changes in IRF
costs and utilization that occur over
time.
Response: We appreciate the
commenters’ suggestions for updating
the data used in the analysis of the CMG
relative weights for FY 2010, and we
agree that we should continue to use the
most recent available data for our
analyses of the CMG relative weights.
However, only about 20 percent of the
FY 2008 IRF cost reports are available
for analysis at this time, and we do not
believe that 20 percent is a large enough
or representative enough sample of all
IRFs on which to base our updates.
Thus, for this final rule, we have
continued to use the most recent
available data, which are the FY 2008
IRF claims and FY 2007 IRF cost report
data. We will continue to update the
CMG relative weights and average
length of stay values in the future, as
appropriate, using the most recent
available data.
Comment: One commenter requested
that CMS seek additional sources of cost
information, such as the Cost Resource
Utilization (CRU) Tool data from the
Post Acute Care Payment Reform
Demonstration (PAC PRD), to address
issues of relative weight compression in
future updates to the CMG relative
weights.
Response: We appreciate the
commenter’s suggestion, and will
consider this suggestion for future
analyses once the CRU data are
complete and available for analysis.
Comment: One commenter stated a
concern that the proposed update to the
CMG relative weights for FY 2010
would result in a slight decrease in the
average payment per case for IRFs and
would increase payments for certain
diagnoses while decreasing payments
for other diagnoses.
Response: Consistent with the way
that we applied updates to the CMG
relative weights and average length of
stay values in the FY 2006 IRF PPS final
rule (70 FR 47880 and 70 FR 57166), the
FY 2007 IRF PPS final rule (71 FR
48354), and the FY 2009 IRF PPS final
rule (73 FR 46370), we are updating the
CMG relative weights and average
length of stay values in this final rule in
a budget-neutral manner, so that
estimated aggregate payments to IRFs do
not increase or decrease as a result of
these updates. Thus, we apply a budgetneutrality factor of 1.0020 to increase
the standard payment conversion factor
(as described in section VI.C of this final
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rule) to counteract any estimated
decrease in aggregate IRF payments as a
result of the updates to the CMG relative
weights and average length of stay
values.
Further, as we stated in the FY 2010
IRF PPS proposed rule (74 FR 21052 at
21059), the updates are generally
expected to result in some increases and
some decreases to the CMG relative
weight values. Changes in the relative
weights are, by definition, distributional
and, therefore, the fact that the updates
shown in Table 1 increase IRF payments
to some diagnoses and decrease IRF
payments to other diagnoses is to be
expected. The intent of these changes is
to ensure that the relative payments
assigned to the CMGs and tiers continue
to reflect the relative costs of caring for
different types of patients in IRFs.
Comment: Several commenters
requested that we reiterate that the
average length of stay values are not
intended to be used as clinical
guidelines for patient care, but are only
used to determine when an IRF
discharge meets the definition of a
short-stay transfer, which results in a
per diem case level adjustment.
Response: We agree with this
comment, and we already stated that the
purpose of the average length of stay
values is to determine when an IRF
discharge meets the definition of a
short-stay transfer in the FY 2010 IRF
PPS proposed rule (74 FR 21052 at
21056). As the commenter notes, the
average length of stay values are not
intended to be used as clinical
guidelines for patient care.
Comment: One commenter suggested
that we consider alternative
methodologies for updating the CMG
relative weights in the future to improve
their ability to predict IRFs’ cost per
case, and expressed a concern about the
need to update the weighted motor
score methodology used to classify IRF
patients into CMGs that was finalized in
the FY 2006 IRF PPS final rule (70 FR
47880 at 47900).
Response: We appreciate the
commenter’s suggestions regarding
alternative methodologies for analyzing
future updates to the CMG relative
weights, and will review them carefully.
We will also take into account the
commenter’s suggestion that we update
the weights used in the motor score
calculation in the future.
Final Decision: After carefully
considering all of the comments that we
received on the proposed updates to the
CMG relative weights and average
length of stay values, we are
implementing the FY 2010 updates to
the CMG relative weights and average
length of stay values presented in Table
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because these final values are based on
analysis of updated FY 2008 data).
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1 below (which are different from the
relative weights and average length of
stay values that we had proposed
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V. Updates to the Facility-Level
Adjustment Factors for FY 2010
A. Updates to the Adjustment Factors
for FY 2010
Section 1886(j)(3)(A)(v) of the Act
confers broad authority upon the
Secretary to adjust the per unit payment
rate ‘‘by such * * * factors as the
Secretary determines are necessary to
properly reflect variations in necessary
costs of treatment among rehabilitation
facilities.’’ For example, we adjust the
Federal prospective payment amount
associated with a CMG to account for
facility-level characteristics such as an
IRF’s LIP percentage, teaching status,
and location in a rural area, if
applicable, as described in § 412.624(e).
In the FY 2010 IRF PPS proposed rule
(74 FR 21052, 21059 through 21062), we
proposed to update the adjustment
factors for calculating the rural, LIP, and
teaching status adjustments based on
the most recent three years worth of IRF
claims data (at that time, FY 2005, FY
2006, and FY 2007) and the most recent
available corresponding IRF cost report
data. Note that, for each IRF claim, we
used the corresponding year’s cost
report data, when available. In the rare
instances in which the corresponding
year’s cost report data were not
available, we used the most recent
available cost report data. For example,
since cost report years are determined
by the start date of the cost report, a
hypothetical IRF’s cost reporting period
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from July 1, 2007 through June 30, 2008
would be referred to as an ‘‘FY 2007’’
cost report. However, the data from this
FY 2007 cost report would
appropriately be matched to IRF
discharges occurring from October 1,
2007 through June 30, 2008 (i.e., during
FY 2008) because these claims would
fall during the period of time covered by
the IRF’s ‘‘FY 2007’’ cost report year. In
the case of FY 2008 claims that would
appropriately match to an IRF’s FY 2008
cost report year, we used the FY 2008
cost report data when available. In
instances in which the matching FY
2008 cost report data were not available,
we used the most recent available data,
which in these cases was the FY 2007
cost report data.
For this final rule, as many
commenters suggested, we are updating
the rural, LIP, and teaching status
adjustment factors using more recent
data (FY 2006, FY 2007, and FY 2008
claims data and the corresponding
year’s cost report data or, if unavailable,
the most recent available cost report
data). We note, however, that we only
have about 20 percent of the IRF cost
reports from FY 2008 available for
analysis at this time, so although we did
use the FY 2008 cost report data that we
had available, in some cases we had to
use a prior year’s cost report data to
match to some of the FY 2008 IRF
claims, as discussed above. Although
the adjustment factors for the rural and
LIP adjustments that we estimate in this
final rule using updated data (18.4
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39773
percent and 0.4613, respectively) do not
differ substantially from the adjustment
factors that we calculated using the
methods set forth in the proposed rule
(18.27 percent and 0.4372, respectively),
the teaching status adjustment factor
that we calculate in this final rule using
updated data (0.6876) is significantly
lower than the teaching status
adjustment factor that we calculated in
the proposed rule (1.0494). This is due
to the relatively large year-to-year
fluctuations in the teaching status
adjustment factor noted in the proposed
rule (74 FR 21052 at 21061).
We believe that it is necessary to
update these adjustment factors at this
time because the adjustment factors that
are being used currently to calculate the
rural, LIP, and teaching status
adjustments are based on FY 2003 data
(as finalized in the FY 2006 IRF PPS
final rule (70 FR 47880, 47928 through
47934)), and the FY 2003 data do not
reflect recent changes in IRF patient
populations resulting from the 60
percent rule and medical review
activities.
The current adjustment factors for the
rural, LIP, and teaching status
adjustments in the FY 2006 IRF PPS
final rule (70 FR 47928 through 47934)
are based on regression analysis by the
RAND Corporation (RAND) using FY
2003 IRF claims and cost report data. In
the FY 2010 IRF PPS proposed rule (74
FR 21052, 21059 through 21062), we
proposed to use the same methodology
RAND used in computing these
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adjustment factors. However, we
proposed to compute the adjustment
factors using three consecutive years of
claims data and the corresponding
year’s cost report data or, when not
available, the most recent available cost
report data and to average the calculated
adjustment factors for all three years to
develop the proposed rural, LIP, and
teaching status adjustment factors for
FY 2010. As discussed in the FY 2010
IRF PPS proposed rule (74 FR 21052,
21059 through 21061), we received a
comment on the FY 2009 IRF PPS
proposed rule (73 FR 22674) suggesting
that we consider a three-year moving
average approach because it would
provide a more stable adjustment factor,
enabling IRFs to project their future
Medicare payments more accurately. We
analyzed the suggestion and agree that
a three year average of the adjustment
factors would promote more stability in
the adjustment factors over time, which
we believe will benefit IRFs by ensuring
reduced variation from year to year and
facilitating IRFs’ long-term budgetary
planning processes.
We received 12 comments on the
proposed updates to the rural, LIP, and
teaching status adjustment factors for
FY 2010, which are summarized below.
Comment: The commenters
overwhelmingly supported the
proposed three-year moving average
approach to updating the rural, LIP, and
teaching status adjustment factors,
saying that this approach makes
payments to IRFs more stable and
predictable over time. The commenters
further requested that CMS continue to
use this methodology to update these
facility-level adjustment factors
annually in the future to ensure that
they continue to reflect the costs of care
in IRFs.
Response: We agree that using the
three-year moving average approach
will provide greater stability and
predictability of Medicare payments for
IRFs, and will finalize this methodology
to update the facility-level adjustment
factors for FY 2010 and future years.
Comment: One commenter expressed
concerns about the proposed decrease in
the rural adjustment factor for FY 2010
and asked us to explain what cost
factors we believe may have caused the
estimated decrease in the rural
adjustment factor.
Response: We believe that it is
important to adjust payments for rural
IRFs to reflect the higher costs that IRFs
in rural areas incur for providing
services in these areas. However, the
results of our analysis using the most
recent available data and the three-year
moving average approach indicate that a
rural adjustment factor of 18.4 percent
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more accurately reflects the current
costs of providing IRF services in rural
areas.
Further, we believe that the estimated
decrease in the rural adjustment factor
for FY 2010 (from 21.3 percent to 18.4
percent) is, in part, the result of
improvements we made to the IRF
classification system in the FY 2006 and
FY 2007 IRF PPS final rules (70 FR
47880, 47886 through 47904 and 71 FR
48354, 48373 through 48374). Those
improvements were designed to account
more appropriately for the variation in
costs among different types of IRF
patients. To the extent that some of the
differences in costs that we previously
observed between rural and urban IRFs
were the result of differences in patient
populations, better accounting for the
variations in costs among patients may
have reduced the need to account for
differences in costs between rural and
urban IRFs.
Comment: The Medicare Payment
Advisory Commission (MedPAC)
suggested that CMS conduct research on
the IRF teaching status adjustment to
determine why the teaching status
adjustment factor appears to vary so
much from year to year, and to evaluate
the accuracy and reliability of the
adjustment. In the meantime, MedPAC
suggested that CMS consider
alternatives to the 3-year moving
average approach, such as maintaining
the IRF teaching adjustment at its FY
2009 level, capping the adjustment at
the level currently in place for IPPS
hospitals or inpatient psychiatric
facilities (IPFs), or capping the
adjustment at a level equal to MedPAC’s
estimate of the empirically justified IME
adjustment for IPPS hospitals. MedPAC
notes that the purpose of these
alternatives would be to either maintain
the teaching status adjustment at its
current level or reduce the adjustment.
Response: As we reported in the FY
2010 IRF PPS proposed rule (74 FR
21052 at 21061), we estimate that the
teaching status adjustment factors
would be 1.5155, 0.6732, and 1.0451
using FY 2005, FY 2006, and FY 2007
data, respectively. In addition, for this
final rule, we estimate that the teaching
status adjustment factor would be
0.4045 using FY 2008 data. We are still
analyzing the reasons for such large
fluctuations in the teaching status
adjustment factors from year to year.
However, we believe that it may be due,
in part, to relatively large fluctuations in
the teaching variable (number of interns
and residents divided by the average
daily census) that we observe in the data
between FY 2005 and FY 2008. On
average, the teaching variable for all
teaching IRFs was 0.1164, 0.1207,
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0.1160, and 0.1295 in FYs 2005, 2006,
2007, and 2008, respectively. We
believe that this variation may reflect
provider responses to the
implementation of the IRF teaching
status adjustment in FY 2006, and that
we may see less variation over time as
IRFs adjust to this new payment
adjustment.
However, to mitigate the impact on
payments of annual fluctuations in the
facility-level adjustment factors, we
have proposed to use and, by this rule,
adopt a three-year moving average
approach instead of using only one
year’s worth of data to calculate the
rural, LIP, and teaching status
adjustment factors for FY 2010. Using
the 3-year moving average approach and
updated IRF claims data from FYs 2006
through 2008, we calculate a teaching
status adjustment factor for this final
rule of 0.6876, which is less than the
factor 0.9012 that was applied to IRF
PPS payments from FY 2006 through FY
2009. Since the teaching status
adjustment factor for this final rule is
lower than the current factor, we do not
believe that it is necessary to consider
the alternative ‘‘capping’’ methodologies
suggested by MedPAC at this time.
However, we will continue to monitor
the data and work with MedPAC to
analyze the reasons for the year-to-year
fluctuations.
Comment: Several commenters
requested that we use FY 2008 IRF
claims and cost report data to update
the facility-level adjustment factors for
FY 2010.
Response: We appreciate the
commenters’ suggestions for updating
the data used in the analysis of the IRF
facility-level adjustment factors for FY
2010, and we agree that we should
continue to use the most recent
available data for these analyses.
However, only about 20 percent of the
FY 2008 IRF cost reports are available
for analysis at this time. Thus, for this
final rule, we have continued to use the
most recent available data, which are
the FY 2006, FY 2007, and FY 2008 IRF
claims data and the corresponding
year’s cost report data or, if unavailable,
the most recent available cost report
data.
Final Decision: After carefully
considering all of the comments that we
received on the proposed updates to the
rural, LIP, and teaching status
adjustment factors for FY 2010,
including the overwhelming support for
the proposed use of a three-year moving
average approach to calculating these
adjustment factors, we are finalizing the
following updates to the rural, LIP, and
teaching status adjustment factors for
FY 2010. Note that these updated
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adjustment factors were calculated
using the same methodology RAND
used in calculating the current
adjustment factors but using updated FY
2006, FY 2007, and 2008 IRF claims
data and the corresponding year’s cost
report data or, if unavailable, the most
recent available cost report data. IRF
PPS payments to IRFs in rural areas will
be increased by 18.4 percent for FY
2010. IRF PPS payments will be
adjusted for FY 2010 to account for the
percentage of low-income patients that
an IRF treats using the updated LIP
39775
adjustment formula of (1 +
disproportionate share hospital (DSH)
patient percentage) raised to the power
of (0.4613), where the DSH patient
percentage for each IRF =
Medicare SSI Days
Medicaid, Non-Medicare Days
+
Total Medicare Days
Total Days
B. Budget Neutrality Methodology for
the Updates to the IRF Facility-Level
Adjustment Factors
Consistent with the way that we
implemented changes to the IRF facilitylevel adjustment factors (the rural, LIP,
and teaching status adjustment factors)
in the FY 2006 IRF PPS final rule (70
FR 47880 and 70 FR 57166), which was
the only year in which we updated
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these adjustment factors, we are
updating the rural, LIP, and teaching
status adjustment factors for FY 2010 in
such a way that total estimated
aggregate payments to IRFs for FY 2010
will be the same with or without the
updates (that is, in a budget neutral
manner) by applying budget neutrality
factors for each of these three changes
to the standard payment amount. To
calculate the budget neutrality factors
used to update the rural, LIP, and
teaching status adjustment factors, we
used the following steps:
Step 1. Using the most recent
available data (currently FY 2008),
calculate the estimated total amount of
IRF PPS payments that would be made
in FY 2010 (without applying the
update to the rural, LIP, or teaching
status adjustment factors).
Step 2. Calculate the estimated total
amount of IRF PPS payments that would
be made in FY 2010 if the update to the
rural adjustment factor were applied.
Step 3. Divide the amount calculated
in step 1 by the amount calculated in
step 2 to determine the budget
neutrality factor (1.0023) that would
maintain the same total estimated
aggregate payments in FY 2010 with and
without the update to the rural
adjustment factor.
Step 4. Calculate the estimated total
amount of IRF PPS payments that would
be made in FY 2010 if the update to the
LIP adjustment factor were applied.
Step 5. Divide the amount calculated
in step 1 by the amount calculated in
step 4 to determine the budget
neutrality factor (1.0192) that would
maintain the same total estimated
aggregate payments in FY 2010 with and
without the update to the LIP
adjustment factor.
Step 6. Calculate the estimated total
amount of IRF PPS payments that would
be made in FY 2010 if the update to the
teaching status adjustment factor were
applied.
Step 7. Divide the amount calculated
in step 1 by the amount calculated in
step 6 to determine the budget
neutrality factor (1.0037) that would
maintain the same total estimated
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aggregate payments in FY 2010 with and
without the update to the teaching
status adjustment factor.
Step 8. Apply the budget neutrality
factors for the updates to the rural, LIP,
and teaching status adjustment factors
to the FY 2009 IRF PPS standard
payment amount after the application of
the budget neutrality factors for the
wage adjustment and the CMG relative
weights.
The budget neutrality factors for the
updates to the rural, LIP, and teaching
status adjustment factors in this final
rule differ from those described in the
proposed rule (74 FR 21052, 21061
through 21062) due to the use of
updated data for the analysis in this
final rule.
In section VI.C of this final rule, we
discuss the methodology for calculating
the final standard payment conversion
factor for FY 2010.
VI. FY 2010 IRF PPS Federal
Prospective Payment Rates
A. Market Basket Increase Factor and
Labor-Related Share for FY 2010
Section 1886(j)(3)(C) of the Act
requires the Secretary to establish an
increase factor that reflects changes over
time in the prices of an appropriate mix
of goods and services included in the
covered IRF services, which is referred
to as a market basket index. According
to section 1886(j)(3)(A)(i) of the Act, the
increase factor shall be used to update
the IRF Federal prospective payment
rates for each FY. Section 115 of the
MMSEA amended section 1886(j)(3)(C)
of the Act to apply a zero percent
increase factor for FYs 2008 and 2009,
effective for IRF discharges occurring on
or after April 1, 2008. In the absence of
any such amendment for FY 2010, we
are updating IRF PPS payments by a
market basket increase factor based
upon the most current data available in
accordance with section 1886(j)(3)(A)(i)
of the Act.
Beginning with the FY 2006 IRF PPS
final rule (70 FR 47908 through 47917),
the market basket index used to update
IRF payments is a 2002-based market
basket reflecting the operating and
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Finally, IRF PPS payments to eligible
IRFs that qualify for the teaching status
adjustment will be adjusted by the
following updated formula for FY 2010:
(1 + full-time equivalent (FTE)
residents/average daily census) raised to
the power of (0.6876). Note that the
rural, LIP, and teaching status
adjustment factors for FY 2010 differ
from those proposed in the FY 2010 IRF
PPS proposed rule (74 FR 21052, 21060
through 21061) due to the use of
updated data in this final rule.
To calculate the updates to the rural,
LIP, and teaching status adjustment
factors for FY 2010, we used the
following steps:
[Steps 1 and 2 are performed
independently for each of three years of
IRF claims data: FY 2006, FY 2007, and
FY 2008]
Step 1. Calculate the average cost per
case for each IRF in the IRF claims data
using the corresponding year’s cost
report data or, if unavailable, the most
recent available cost report data, as
described above.
Step 2. Use logarithmic regression
analysis on average cost per case to
compute the coefficients for the rural,
LIP, and teaching status adjustments.
Step 3. Calculate a simple mean for
each of the coefficients across the three
years of data using logarithms for the
LIP and teaching status adjustment
coefficients (because they are
continuous variables) but not using
logarithms for the rural adjustment
coefficient (because the rural variable is
1 if the facility is rural and zero
otherwise). To compute the LIP and
teaching status adjustment factors, we
convert these factors back out of the
logarithmic form.
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capital cost structures for freestanding
IRFs, freestanding inpatient psychiatric
facilities (IPFs), and long-term care
hospitals (LTCHs) (hereafter referred to
as the rehabilitation, psychiatric, and
long-term care (RPL) market basket).
For this final rule, we have used the
same methodology described in the FY
2006 IRF PPS Final Rule (70 FR 47908
through 47917) to compute the FY 2010
market basket increase factor and laborrelated share. Using this method and the
IHS Global Insight, Inc. forecast for the
second quarter of 2009 of the 2002based RPL market basket, the FY 2010
IRF market basket increase factor is 2.5
percent. IHS Global Insight is an
economic and financial forecasting firm
that contracts with CMS to forecast the
components of providers’ market
baskets.
Also, using the methodology
described in the FY 2006 IRF PPS final
rule (70 FR 47880, 47908 through
47917), we are updating the IRF laborrelated share for FY 2010. Using this
method and the IHS Global Insight, Inc.
forecast for the second quarter of 2009
of the 2002-based RPL market basket,
the IRF labor-related share for FY 2010
is the sum of the FY 2010 relative
importance of each labor-related cost
category. This figure reflects the
different rates of price change for these
cost categories between the base year
(FY 2002) and FY 2010. Consistent with
our proposal to update the labor-related
share with the most recent available
data, the labor-related share for this
final rule reflects IHS Global Insight’s
second quarter 2009 forecast of the
2002-based RPL market basket. As
shown in Table 2, the FY 2010 laborrelated share is 75.779 percent.
TABLE 2—FY 2010 IRF RPL LABORRELATED SHARE RELATIVE IMPORTANCE
Cost category
FY 2010
IRF laborrelated
share
relative
importance
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Wages and salaries ..................
Employee benefits ....................
Professional fees ......................
All other labor intensive services ........................................
52.892
13.949
2.873
Subtotal .............................
Labor-related share of capital
costs (.46) .............................
71.841
Total ...................................
75.779
2.127
3.938
Source: IHS GLOBAL INSIGHT, INC, 2nd
QTR, 2009; @USMACRO/CONTROL0609
@CISSIM/TL0509.SIM Historical Data through
1st QTR, 2009.
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We received 10 comments on the
proposed updates to the IRF market
basket increase factor and labor-related
share for FY 2010, which are
summarized below.
Comment: One commenter supported
the creation of a stand-alone IRF market
basket based on both freestanding and
hospital-based cost report data. The
commenter offered the following
suggestions that CMS could pursue in
order to account for the differences in
costs between the two facility types.
Those suggestions included:
1. To survey a random sample of
facilities to assess the presence of the
array of rehabilitation services that may
be available through the freestanding
IRF as compared to a hospital-based
IRF.
2. To conduct detailed interviews of
the Chief Financial Officers (CFOs) of
freestanding versus hospital based units
to understand the differences in the
ways IRF costs are accounted for in cost
reports.
Response: We appreciate the
commenter’s response concerning the
stand-alone IRF market basket and the
suggestions that were provided. CMS
will take the suggestions into
consideration as we continue to
research the differences between
hospital-based and freestanding
facilities.
Comment: Several commenters noted
that the use of 2002 data is
inappropriate because of major changes
to IRF case mix and patient severity and
requested CMS update the cost weights
of the existing RPL market basket to a
more recent base year.
Response: We recognize the
commenters’ concerns regarding the
continued use of 2002 data in the RPL
market basket. We have focused our
recent efforts on comparing and
contrasting the costs and cost structures
of freestanding and hospital-based IRFs,
including the effects of changes to case
mix and patient severity over the last
several years. We will consider the
suggestions that we received during the
comment period to better understand
those differences (and further
investigate the appropriateness of
creating a stand-alone IRF market
basket), as well as examine the
appropriateness of rebasing and revising
the RPL market basket.
Comment: One commenter noted that
the data used to calculate the RPL
market basket are obtained from
freestanding IRFs, freestanding IPFs,
and LTCHs. The commenter expressed
the concern that each facility type
requires different resources and thus
combining the three types of facilities
distorts the cost structures of IRFs. This
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commenter also suggested incorporating
the most recent available data into the
market basket.
Response: CMS recognizes the
existence of differences in cost
structures across freestanding IPFs,
freestanding IRFs, and LTCHs. However,
pending further research into the
viability of creating a stand-alone IRF
market basket, we feel that it is
appropriate to continue to use the
current 2002-based RPL market basket
to update IRF payments. We will
examine the appropriateness of rebasing
and revising the RPL market basket for
the future.
Comment: Several commenters
offered that one reason for the difference
between freestanding and hospitalbased IRFs cost structures is that most
hospital-based units are smaller than
freestanding IRFs. For example, one
commenter indicated that hospitalbased IRFs have nearly two-thirds fewer
discharges than freestanding IRFs. Thus,
the commenters claimed that hospitalbased IRFs may be unable to achieve the
same level of economies of scale as
freestanding IRFs can.
Response: We have noted that cost
differences between hospital-based and
freestanding IRFs may be due to the
volume of care that hospital-based
facilities provide relative to freestanding
facilities. In an attempt to control for
differences in the volume of services,
we have compared costs per discharge
and costs per day between the two
facility types and continue to find
differences in their overall cost levels.
Notably, CMS feels that, all other things
held constant, differing volumes may
not necessarily explain differing cost
structures as the cost weights reflect the
relative expense of one category to
another within a facility. We will
continue to evaluate our findings related
to these metrics with new data as it
becomes available.
Comment: One commenter mentioned
that one contributing cause of the
difference in cost structures between
freestanding and hospital-based IRFs is
the issue of costs being allocated down
from the IPPS hospital to the hospitalbased IRF unit.
Response: We share the commenter’s
concern that overhead costs from the
host hospital may be skewing the
hospital-based unit’s costs and cost
structure. One of the main reasons why
CMS has historically relied on Medicare
cost report data from freestanding
facilities to construct the market baskets
is our concern over the distribution of
the host hospital’s overhead costs to the
sub-provider units. We will continue to
investigate the allocation of overhead
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costs from the host hospital to the
hospital-based IRF unit.
Comment: One commenter
acknowledged that seeking outside
input regarding differences in cost
structures between hospital-based and
freestanding IRFs is appropriate.
However, the commenter urged CMS to
proceed with caution as it may be
difficult for CMS to confirm that the
methods used to collect outside data are
sound and that the data are
representative of the industry as a
whole. The commenter also stated that
CMS should ultimately determine
whether the market basket should in
fact be based on the cost structure of
hospital-based and freestanding IRFs
instead of just one type of facility if the
higher costs cannot be explained by
differences in case mix and other
patient characteristics.
Response: As stated in the proposed
rule, we do not feel it is appropriate to
move forward on the creation of a standalone IRF market basket until such time
that we can adequately explain the
differences in costs and cost structures
between hospital-based IRFs and
freestanding IRFs. We agree with the
commenter that any information from
the public should be carefully
examined. We reached out to the public
for information to help us better
understand these differences, but we
agree with the commenter that
regardless of the information we receive,
we will have to evaluate thoroughly the
appropriateness and independent nature
of any data provided.
Comment: A couple of commenters
stated that hospital-based IRFs
experience different levels of costs due
to the types of patients admitted and
services that occur during the IRF
hospitalization. They commented that
hospital-based IRFs receive more
medically fragile patients due to the
unit’s immediate access to a variety of
physician specialties and specialized
treatments. The commenter suggested
investigating the ICD–9 code differences
between hospital-based and
freestanding IRFs.
Response: We have looked into case
mix differences between free-standing
and hospital-based facilities. The
average case mix is lower in hospitalbased units than in freestanding units
for the years we examined (2005–2007).
We will continue to monitor differences
in case mix (as we believe case-mix
indexes for freestanding and hospitalbased facilities account for the
differences in patient severity). We will
also explore the viability of an ICD–9
code analysis.
Comment: One commenter supports
CMS in the endeavor of creating a stand-
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alone IRF market basket to replace the
RPL market basket. The commenter
expressed willingness to assist the
agency in its analysis. The commenter
provided the following
recommendations for future research:
• To examine the cost differences
between freestanding and hospitalbased IRFs, as well as the differences
between IRFs and other hospitals such
as Inpatient Psychiatric Hospitals (IPFs)
and Long Term Care Facilities.
• To determine to what extent fewer
economies-of-scale and cost allocation
differences account for cost differences
between freestanding and hospitalbased IRFs.
• To determine whether different
classes of IRFs have different providerto-patient ratios.
• To investigate if differences in
patient severity exist between the two
classes of facilities and if so, to what
extent does higher severity correlate
with higher nursing and rehabilitation
costs.
Response: We appreciate the response
concerning the stand-alone IRF market
basket and the suggestions the
commenter provided. We will be
continuing our efforts to study cost
differences between hospital-based and
freestanding IRFs, as well as differences
between IRFs, IPFs, and Long-Term Care
Hospitals. We have attempted to control
for differences in volume between the
freestanding and hospital-based IRFs by
analyzing costs per discharge and costs
per day. As yet, controlling for patient
volume using these metrics has not
yielded very much insight into the
differences. We will continue to
examine other ways to determine if
economies of scale are able to provide
explanatory information on the
differences we observe. Finally, we will
look more in-depth at the commenter’s
additional suggestions.
Comment: One commenter had
concerns regarding the lower than usual
increase in the 2010 market basket
update. The commenter asserts that
health care organizations are still
required to provide the same care to
patients as in more economically stable
periods and feels that it is unsafe to
assume that hospitals can operate at a
lower level of costs while providing the
same high level of care simply because
the inflation indicators predict a
slowing economy.
The commenter supports the
American Hospital Association’s
(AHA’s) suggestion that CMS should
make the required market basket
adjustments without revising the price
proxies used in the calculation which
indicate potentially lower costs to the
hospitals.
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39777
Response: The 2.5 percent update
found in this final rule does not assume
a lower cost level from the prior year for
the IRF industry. The intent of the RPL
market basket is to estimate the input
price pressures that providers will face
in their respective payment years. The
projected RPL market basket of 2.5
percent, then, reflects our most recent
price projections for the various goods
and services that IRF providers require
in order to provide inpatient
rehabilitation services in FY 2010.
Additionally, the commenter noted
that IRFs have more patients without
insurance and are likely to incur a
higher level of bad debt. This comment
is outside the scope of the market basket
update, since bad debt is reimbursed
outside of the market basket update
factor.
Lastly, we think the commenter may
have confused the AHA comments with
regard to the IPPS market basket and the
revision of various price proxies. IRF
facilities will continue to receive a
market basket update based on the RPL
market basket. We have not made any
technical changes to the composition of
the RPL market basket. As such, the
commenter’s request that CMS should
not revise the price proxies for this
market basket is not applicable.
Comment: One commenter noted
concern with the way CMS estimates
the labor-related share for IRF facilities.
The commenter specifically expressed
concern that the price proxies are based
on FY 2002 data and prior to that were
last updated in FY 1992. This
commenter feels that the 2002 data do
not reflect the effects of the 60-percent
rule, implemented in CY 2004, and
recommends that CMS update the price
proxies more frequently to ensure the
labor share is accurately calculated.
Response: We believe the commenter
may be confusing the term price proxy
with the term cost weight. We will
assume for purposes of this response
that the commenter intended to use the
word cost weight rather than price
proxy. We assume this confusion
because the price proxies are not based
on FY 2002 data, and, while the LRS is
based on the relative importance (a
combination of the cost weight and
price proxies), it is not based solely on
price proxies. Our price proxy
projections are updated on a quarterly
basis. Price proxies are subject to
revision under limited circumstances. A
revision to a price proxy in a market
basket could occur if the price index is
discontinued or if the agency producing
the price proxy (usually the Bureau of
Labor Statistics) pulls an index from
publication for statistical viability
reasons. If an index is discontinued,
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then CMS would have to find a
replacement price proxy. Normally,
revisions to the price indexes included
in a market basket are only made when
the market basket is rebased.
Regarding the 60-percent rule, we are
sensitive to the potential impact that the
implementation of this rule may have
on the cost structures of certain
providers. As noted in a previous
comment, we have focused our recent
efforts on comparing and contrasting the
costs and cost structures of freestanding
and hospital-based IRFs. We will be
continuing that analysis, as well as
exploring the appropriateness of
rebasing and revising the market basket
used to update IRF payments whether
that is in the form of the RPL market
basket or a stand-alone IRF market
basket.
Final Decision: We will update IRF
PPS payments by a market basket
increase factor (of 2.5 percent for FY
2010) based upon the most current data
available, in accordance with section
1886(j)(3)(A)(i) of the Act. Further, we
will update the IRF labor-related share
using our current methodology and the
most recent available data. Thus, for this
final rule, the labor-related share is
75.779 percent. This is based on the IHS
Global Insight Inc. forecast for the
second quarter of 2009 (2009Q2) with
historical data through the first quarter
of 2009 (2009Q1).
As we noted in the proposed rule (74
FR 21052 at 21062), we are interested in
exploring the possibility of creating a
stand-alone IRF market basket that
reflects the cost structures of only IRF
providers. As part of our consideration
of a stand-alone IRF market basket, we
solicited information from the public in
the proposed rule that might help us to
better understand the underlying
reasons for the variations in cost
structure between freestanding and
hospital-based IRFs. Due to the need for
further research regarding the
differences in costs and cost structures
between hospital-based IRFs and
freestanding IRFs, we are not pursuing
a stand-alone IRF market basket at this
time.
B. Area Wage Adjustment
Section 1886(j)(6) of the Act requires
the Secretary to adjust the proportion
(as estimated by the Secretary from time
to time) of rehabilitation facilities’ costs
attributable to wages and wage-related
costs by a factor (established by the
Secretary) reflecting the relative hospital
wage level in the geographic area of the
rehabilitation facility compared to the
national average wage level for those
facilities. The Secretary is required to
update the IRF PPS wage index on the
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basis of information available to the
Secretary on the wages and wage-related
costs to furnish rehabilitation services.
Any adjustments or updates made under
section 1886(j)(6) of the Act for a FY are
made in a budget neutral manner.
In the FY 2009 IRF PPS final rule (73
FR 46370 at 46378), we maintained the
methodology described in the FY 2006
IRF PPS final rule to determine the wage
index, labor market area definitions, and
hold harmless policy consistent with
the rationale outlined in the FY 2006
IRF PPS final rule (70 FR 47880, 47917
through 47933).
In the FY 2010 IRF PPS proposed rule
(74 FR 21052, 21062 through 21063), we
proposed to maintain the policies and
methodologies described in the FY 2009
IRF PPS final rule relating to the labor
market area definitions and the wage
index methodology for areas with wage
data. Thus, we proposed to use the
CBSA labor market area definitions and
the pre-reclassification and pre-floor
hospital wage index data based on 2005
cost report data.
The labor market designations made
by the Office of Management and
Budget (OMB) include some geographic
areas where there are no hospitals and,
thus, no hospital wage index data on
which to base the calculation of the IRF
PPS wage index. We proposed to
continue to use the same methodology
discussed in the FY 2008 IRF PPS final
rule (72 FR 44284 at 44299) to address
those geographic areas where there are
no hospitals and, thus, no hospital wage
index data on which to base the
calculation of the FY 2010 IRF PPS
wage index.
Additionally, we proposed to
incorporate the CBSA changes
published in the most recent OMB
bulletin that applies to the hospital
wage data used to determine the current
IRF PPS wage index. The changes were
nominal and did not represent
substantive changes to the CBSA-based
designations. Specifically, OMB added
or deleted certain CBSA numbers and
revised certain titles. The OMB bulletins
are available online at https://
www.whitehouse.gov/omb/bulletins/
index.html.
To calculate the wage-adjusted facility
payment for the payment rates set forth
in this final rule, we multiply the
unadjusted Federal payment rate for
IRFs by the FY 2010 RPL labor-related
share (75.779 percent) to determine the
labor-related portion of the standard
payment amount. We then multiply the
labor-related portion by the applicable
IRF wage index from the tables in the
addendum to this final rule. Table 1 is
for urban areas, and Table 2 is for rural
areas.
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Adjustments or updates to the IRF
wage index made under section
1886(j)(6) of the Act must be made in a
budget neutral manner. We calculate a
budget neutral wage adjustment factor
as established in the FY 2004 IRF PPS
final rule (68 FR 45674 at 45689),
codified at § 412.624(e)(1), as described
in the steps below. We use the listed
steps to ensure that the FY 2010 IRF
standard payment conversion factor
reflects the update to the wage indexes
(based on the FY 2005 hospital cost
report data) and the labor-related share
in a budget neutral manner:
Step 1. Determine the total amount of
the estimated FY 2009 IRF PPS rates,
using the FY 2009 standard payment
conversion factor and the labor-related
share and the wage indexes from FY
2009 (as published in the FY 2009 IRF
PPS final rule (73 FR 46370 at 44301,
44298, and 44312 through 44335,
respectively)).
Step 2. Calculate the total amount of
estimated IRF PPS payments using the
FY 2009 standard payment conversion
factor and the FY 2010 labor-related
share and CBSA urban and rural wage
indexes.
Step 3. Divide the amount calculated
in step 1 by the amount calculated in
step 2. The resulting quotient is the FY
2010 budget neutral wage adjustment
factor of 1.0011.
Step 4. Apply the FY 2010 budget
neutral wage adjustment factor from
step 3 to the FY 2009 IRF PPS standard
payment conversion factor after the
application of the estimated market
basket update to determine the FY 2010
standard payment conversion factor.
We received 3 comments on the
proposed FY 2010 IRF PPS wage index,
which are summarized below.
Comment: Several commenters
recommended that we consider wage
index policies under the current IPPS
because IRFs compete in a similar labor
pool as acute care hospitals. The IPPS
wage index policies would allow IRFs to
benefit from the IPPS reclassification
and/or floor policies. Several
commenters also recommended that
CMS conduct further analysis of the
wage index methodology to ensure that
fluctuations in the annual wage index
for hospitals are minimized, that all
future updates match the costs of labor
in the market, that IRF’s occupational
mix is appropriately recognized, and
that payments are ‘‘smoothed’’ across
geography and across time.
Response: We note that the IRF PPS
does not account for geographic
reclassification under sections
1886(d)(8) and (d)(10) of the Act and
does not apply the ‘‘rural floor’’ under
section 4410 of Public Law 105–33
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(BBA). Because we do not have an IRF
specific wage index, we are unable to
determine at this time the degree, if any,
to which a geographic reclassification
adjustment under the IRF PPS is
appropriate. Furthermore, we believe
the ‘‘rural floor’’ is applicable only to
the acute care hospital payment system.
The rationale for our current wage index
policies is fully described in the FY
2006 final rule (70 FR 47880, 47926
through 47928).
In addition, we reviewed the
Medicare Payment Advisory
Commission’s (MedPAC) wage index
recommendations as discussed in
MedPAC’s June 2007 report titled,
‘‘Report to Congress: Promoting Greater
Efficiency in Medicare.’’ Although some
commenters recommended that we
adopt the IPPS wage index policies such
as reclassification and floor policies, we
note that MedPAC’s June 2007 report to
Congress recommends that Congress
‘‘repeal the existing hospital wage index
statute, including reclassification and
exceptions, and give the Secretary
authority to establish new wage index
systems.’’ We believe that adopting the
IPPS wage index policies, such as
reclassification or floor, would not be
prudent at this time because MedPAC
suggests that the reclassification and
exception policies in the IPPS wage
index alters the wage index values for
one-third of IPPS hospitals. In addition,
MedPAC found that the exceptions may
lead to anomalies in the wage index. By
adopting the IPPS reclassifications and
exceptions at this time, the IRF PPS
wage index could be vulnerable to
similar issues that MedPAC identified
in the June 2007 Report to Congress.
However, we will continue to review
and consider MedPAC’s
recommendations on a refined or an
alternative wage index methodology for
the IRF PPS in future years.
In addition, we have research
currently under way to examine
alternatives to the wage index
methodology, including the issues the
commenters mentioned about ensuring
that the wage index minimizes
fluctuations, matches the costs of labor
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in the market, and provides for a single
wage index policy. Section 106(b)(2) of
the MIEA–TRHCA instructed the
Secretary of Health and Human Services
to take into account MedPAC’s
recommendations on the Medicare wage
index classification system and to
include in the FY 2009 IPPS proposed
rule one or more proposals to revise the
wage index adjustment applied under
section 1886(d)(3)(E) of the Act for
purposes of the IPPS. The proposal (or
proposals) were to consider each of the
following:
• Problems associated with the
definition of labor markets for the wage
index adjustments.
• The modification or elimination of
geographic reclassifications and other
adjustments.
• The use of Bureau of Labor
Statistics data or other data or
methodologies to calculate relative
wages for each geographic area.
• Minimizing variations in wage
index adjustments between and within
MSAs and statewide rural areas.
• The feasibility of applying all
components of CMS’s proposal to other
settings.
• Methods to minimize the volatility
of wage index adjustments while
maintaining the principle of budget
neutrality.
• The effect that the implementation
of the proposal would have on health
care providers in each region of the
country.
• Methods for implementing the
proposal(s), including methods to phase
in such implementations.
• Issues relating to occupational mix,
such as staffing practices and any
evidence on quality of care and patient
safety, including any recommendations
for alternative calculations to the
occupational mix.
To assist us in meeting the
requirements of section 106(b)(2) of
Public Law 109–432, in February 2008
we awarded a contract to Acumen, LLC.
The contractor conducted a study of
both the current methodology used to
construct the Medicare wage index and
the recommendations reported to
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39779
Congress by MedPAC. Part 1 of
Acumen’s final report, which analyses
the strengths and weaknesses of the data
sources used to construct the CMS and
MedPAC indexes, is available online at
https://www.acumenllc.com/reports/cms.
MedPAC’s recommendations were
presented in the FY 2009 IPPS final rule
(https://edocket.access.gpo.gov/2008/
pdf/E8-17914.pdf). We plan to monitor
these efforts and the impact or influence
they may have to the IRF PPS wage
index.
Final Decision: We will continue to
use the policies and methodologies
described in the FY 2009 IRF PPS final
rule relating to the labor market area
definitions and the wage index
methodology for areas with wage data.
Therefore, this final rule continues to
use the Core-Based Statistical Area
(CBSA) labor market area definitions
and the pre-reclassification and prefloor hospital wage index data based on
2005 cost report data. We discuss the
final standard payment conversion
factor for FY 2010 in the next section.
C. Description of the Final IRF Standard
Payment Conversion Factor and
Payment Rates for FY 2010
To calculate the final standard
payment conversion factor for FY 2010,
as illustrated in Table 4 below, we begin
by applying the estimated market basket
increase factor for FY 2010 (2.5 percent)
to the standard payment conversion
factor for FY 2009 ($12,958), which
would equal $13,282. Then, we apply
the budget neutrality factor for the FY
2010 wage index and labor related share
of 1.0011, which would result in a
standard payment amount of $13,297.
Then, we apply the budget neutrality
factor for the revised CMG relative
weights of 1.0020, which would result
in a standard payment amount of
$13,324. Finally, we apply the budget
neutrality factors for the updates to the
rural, LIP, and IRF teaching status
adjustments of 1.0023, 1.0192, and
1.0037, respectively, which would
result in the final FY 2010 standard
payment conversion factor of $13,661.
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After the application of the CMG
relative weights described in section IV
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of this final rule, the resulting
unadjusted IRF prospective payment
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rates for FY 2010 are shown below in
Table 4, ‘‘FY 2010 Payment Rates.’’
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We received 4 comments on the
proposed standard payment conversion
factor and payment rates for FY 2010,
which are summarized below.
Comment: Several commenters
suggested that we add the estimated
market basket increases for FYs 2008
and 2009 back into the standard
payment conversion factor before we
update it for FY 2010.
Response: We do not believe that this
is the intent of the statute. As discussed
above, section 115 of the MMSEA
amended section 1886(j)(3)(C) of the Act
to apply a zero percent increase factor
for FYs 2008 and 2009, effective for IRF
discharges occurring on or after April 1,
2008. For subsequent fiscal years,
section 1886(j)(3)(C) of the Act requires
the Secretary to establish an increase
factor that reflects changes over time in
the prices of an appropriate mix of
goods and services included in the
covered IRF services, which is referred
to as a market basket index. According
to section 1886(j)(3)(A)(i) of the Act, this
increase factor shall be used to update
the IRF Federal prospective payment
rates for each FY. In accordance with
these provisions of the statute, we will
update IRF PPS payments by a market
basket increase factor for FY 2010 based
upon the most current available data.
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D. Example of the Methodology for
Adjusting the Federal Prospective
Payment Rates
Table 5 illustrates the methodology
for adjusting the Federal prospective
payments (as described in sections VI.A
through VI.C of this final rule). The
examples below are based on two
hypothetical Medicare beneficiaries,
both classified into CMG 0110 (without
comorbidities). The unadjusted Federal
prospective payment rate for CMG 0110
(without comorbidities) appears in
Table 4 above.
One beneficiary is in Facility A, an
IRF located in rural Spencer County,
Indiana, and another beneficiary is in
Facility B, an IRF located in urban
Harrison County, Indiana. Facility A, a
rural non-teaching hospital has a DSH
percentage of 5 percent (which would
result in a LIP adjustment of 1.0228), a
wage index of 0.8473, and a rural
adjustment of 18.4 percent. Facility B,
an urban teaching hospital, has a DSH
percentage of 15 percent (which would
result in a LIP adjustment of 1.0666), a
wage index of 0.9249, and a teaching
status adjustment of 0.0610.
To calculate each IRF’s labor and nonlabor portion of the Federal prospective
payment, we begin by taking the
unadjusted Federal prospective
payment rate for CMG 0110 (without
comorbidities) from Table 4 above.
Then, we multiply the estimated laborrelated share (75.779) described in
section VI.A of this final rule by the
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unadjusted Federal prospective
payment rate. To determine the nonlabor portion of the Federal prospective
payment rate, we subtract the labor
portion of the Federal payment from the
unadjusted Federal prospective
payment.
To compute the wage-adjusted
Federal prospective payment, we
multiply the labor portion of the Federal
payment by the appropriate wage index
found in the addendum in Tables 1 and
2. The resulting figure is the wageadjusted labor amount. Next, we
compute the wage-adjusted Federal
payment by adding the wage-adjusted
labor amount to the non-labor portion.
Adjusting the wage-adjusted Federal
payment by the facility-level
adjustments involves several steps.
First, we take the wage-adjusted Federal
prospective payment and multiply it by
the appropriate rural and LIP
adjustments (if applicable). Second, to
determine the appropriate amount of
additional payment for the teaching
status adjustment (if applicable), we
multiply the teaching status adjustment
(1.0706, in this example) by the wageadjusted and rural-adjusted amount (if
applicable). Finally, we add the
additional teaching status payments (if
applicable) to the wage, rural, and LIPadjusted Federal prospective payment
rates. Table 5 illustrates the components
of the adjusted payment calculation.
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Thus, the adjusted payment for
Facility A would be $31,057.56 and the
adjusted payment for Facility B would
be $30,841.87.
VII. Update to Payments for High-Cost
Outliers Under the IRF PPS
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A. Update to the Outlier Threshold
Amount for FY 2010
Section 1886(j)(4) of the Act provides
the Secretary with the authority to make
payments in addition to the basic IRF
prospective payments for cases
incurring extraordinarily high costs. A
case qualifies for an outlier payment if
the estimated cost of the case exceeds
the adjusted outlier threshold. We
calculate the adjusted outlier threshold
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by adding the IRF PPS payment for the
case (that is, the CMG payment adjusted
by all of the relevant facility-level
adjustments) and the adjusted threshold
amount (also adjusted by all of the
relevant facility-level adjustments).
Then, we calculate the estimated cost of
a case by multiplying the IRF’s overall
cost-to-charge ratio (CCR) by the
Medicare allowable covered charge. If
the estimated cost of the case is higher
than the adjusted outlier threshold, we
make an outlier payment for the case
equal to 80 percent of the difference
between the estimated cost of the case
and the outlier threshold.
In the FY 2002 IRF PPS final rule (66
FR 41316, 41362 through 41363), we
discussed our rationale for setting the
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outlier threshold amount for the IRF
PPS so that estimated outlier payments
would equal 3 percent of total estimated
payments. For the 2002 IRF PPS final
rule, we analyzed various outlier
policies using 3, 4, and 5 percent of the
total estimated payments, and we
concluded that an outlier policy set at
3 percent of total estimated payments
would optimize the extent to which we
could reduce the financial risk to IRFs
of caring for high-cost patients, while
still providing for adequate payments
for all other (non-high cost outlier)
cases.
Subsequently, we updated the IRF
outlier threshold amount in the FYs
2006, 2007, 2008, and 2009 IRF PPS
final rules (70 FR 47880, 70 FR 57166,
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71 FR 48354, 72 FR 44284, and 73 FR
46370, respectively) to maintain
estimated outlier payments at 3 percent
of total estimated payments. We also
stated in the FY 2009 final rule (FR 73
46287) that we would continue to
analyze the estimated outlier payments
for subsequent years and adjust the
outlier threshold amount as appropriate
to maintain the 3 percent target.
In the FY 2010 IRF PPS proposed rule
(74 FR 21052 at 21066), we proposed to
use updated data for calculating the
high-cost outlier threshold amount.
Specifically, we proposed to use FY
2007 claims data using the same
methodology that we used to set the
initial outlier threshold amount in the
FY 2002 IRF PPS final rule (66 FR
41316, 41362 through 41363), which is
also the same methodology that we used
to update the outlier threshold amounts
for FYs 2006 through 2009.
Updated analysis of FY 2008 claims
data using the same methodology that
we used to set the initial outlier
threshold amount in FY 2002 shows
that IRF outlier payments as a
percentage of total estimated payments
are 3 percent in FY 2009. Therefore,
since we estimate that we have achieved
the target percentage in FY 2009, we are
adjusting the outlier threshold amount
in this final rule solely to account for
the 2.5 percent market basket
adjustment for FY 2010 (as discussed in
section VI.A of this rule) and the FY
2010 updates to the facility-level
adjustments (as discussed in section V
of this rule) so that we will continue to
maintain estimated outlier payments at
3 percent of total estimated aggregate
IRF payments for FY 2010.
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B. Update to the IRF Cost-to-Charge
Ratio Ceilings
In accordance with the methodology
stated in the FY 2004 IRF PPS final rule
(68 FR 45674, 45692 through 45694), we
apply a ceiling to IRFs’ cost-to-charge
ratios (CCRs). Using the methodology
described in that final rule, we proposed
in the FY 2010 IRF PPS proposed rule
(74 FR 21052, 21066 through 21067) to
update the national urban and rural
CCRs for IRFs, as well as the national
CCR ceiling for FY 2010, based on
analysis of the most recent data that is
available. We apply the national urban
and rural CCRs in the following
situations:
• New IRFs that have not yet
submitted their first Medicare cost
report.
• IRFs whose overall CCR is in excess
of the national CCR ceiling for FY 2010,
as discussed below.
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• Other IRFs for which accurate data
to calculate an overall CCR are not
available.
Specifically, for FY 2010, we
estimated a national average CCR of
0.622 for rural IRFs, which we calculate
by taking an average of the CCRs for all
rural IRFs using their most recently
submitted cost report data. Similarly,
we estimate a national CCR of 0.494 for
urban IRFs, which we calculate by
taking an average of the CCRs for all
urban IRFs using their most recently
submitted cost report data. We apply
weights to both of these averages using
the IRFs’ estimated costs, meaning that
the CCRs of IRFs with higher costs
factor more heavily into the averages
than the CCRs of IRFs with lower costs.
For this final rule, we have used the
most recent available cost report data
(FY 2007). This includes all IRFs whose
cost reporting periods begin on or after
October 1, 2006, and before October 1,
2007. If, for any IRF, the FY 2007 cost
report was missing or had an ‘‘as
submitted’’ status, we used data from a
previous fiscal year’s settled cost report
for that IRF. However, we do not use
cost report data from before FY 2004 for
any IRF because changes in IRF
utilization since FY 2004 resulting from
the 60 percent rule and IRF medical
review activities suggest that these older
data do not adequately reflect the
current cost of care.
In addition, in light of the analysis
described below, we are setting the
national CCR ceiling at 3 standard
deviations above the mean CCR. The
national CCR ceiling is set at 1.61 for FY
2010. This means that, if an individual
IRF’s CCR exceeds this ceiling of 1.61
for FY 2010, we would replace the IRF’s
CCR with the appropriate national
average CCR (either rural or urban,
depending on the geographic location of
the IRF). We calculated the national
CCR ceiling by:
Step 1. Taking the national average
CCR (weighted by each IRF’s total costs,
as discussed above) of all IRFs for which
we have sufficient cost report data (both
rural and urban IRFs combined);
Step 2. Estimating the standard
deviation of the national average CCR
computed in step 1;
Step 3. Multiplying the standard
deviation of the national average CCR
computed in step 2 by a factor of 3 to
compute a statistically significant
reliable ceiling; and
Step 4. Adding the result from step 3
to the national average CCR of all IRFs
for which we have sufficient cost report
data, from step 1.
We received 4 comments on the
proposed update to payments for high-
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cost outliers under the IRF PPS, which
are summarized below.
Comment: The majority of
commenters said that they support
maintaining estimated outlier payments
at 3 percent of total estimated payments
for FY 2010. However, one commenter
suggested that we reduce the estimated
percentage of outlier payments to 1.5
percent or that we ‘‘hold back’’ a
proportion of outlier payments from
certain IRFs, particularly those IRFs that
might have higher costs because of
decreases in patient volumes. This
commenter expressed concerns that the
IRF outlier policy may be inadvertently
rewarding IRFs for inefficiencies and
suggested that we conduct an analysis of
the distribution of outlier payments
among IRFs.
Response: We will continue to
monitor our IRF outlier policies to
ensure that they continue to compensate
IRFs for treating unusually high-cost
patients and, thereby, promote access to
care for patients who are likely to
require unusually high-cost care. At this
time, however, we do not have any
indications to suggest that the outlier
pool would be better set at 1.5 percent
than at 3 percent, or that it would be
appropriate to ‘‘hold back’’ outlier
payments from individual IRFs. To the
extent that patient volumes in some
IRFs have been declining due to recent
changes in the 60 percent rule and
increased medical review activities, and
that such declines in patient volumes
may have led to temporary cost
increases (due to the allocation of fixed
costs across a smaller number of
patients), we believe that the patient
volumes will soon stabilize and that
fixed costs will decline once IRFs have
had time to adapt to the changes.
However, we will carefully consider this
commenter’s suggestions, and will
consider proposing additional
refinements to the IRF outlier policies in
the future if we find that such
refinements are necessary.
Comment: Several commenters
suggested that we use the FY 2008 IRF
claims data to estimate the IRF outlier
threshold amount for FY 2010.
Response: We agree that we should
use the most recent available data to
estimate the IRF outlier threshold
amount for FY 2010, and have therefore
used the FY 2008 IRF claims data in the
analysis for this final rule.
Comment: One commenter requested
that CMS provide additional
information to the public in the future
to allow the IRF industry and external
researchers to conduct a more thorough
review of CMS’s proposed updates to
the outlier threshold amount and to
verify our estimates of outlier payments
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as a percentage of total payments for FY
2010. This commenter also requested
that we report the actual outlier
payments and outlier payments as a
percentage of total payments for each
FY in this final rule.
Response: We will continue to
provide as much information as possible
to allow the public to analyze and
evaluate our proposed updates to the
IRF outlier threshold amount. In Table
6 below, we provide the requested
information, by FY.
TABLE 6—IRF OUTLIER PAYMENTS
AND OUTLIER PAYMENTS AS A PERCENTAGE OF TOTAL PAYMENTS
Outlier
payments
2003
2004
2005
2006
2007
2008
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Fiscal year
Outlier payments as a
percentage of
total payments
204,193,300
127,308,080
116,534,084
247,632,386
267,474,895
248,047,991
..........
..........
..........
..........
..........
..........
3.3
1.9
1.8
4.0
4.5
4.2
Comment: One commenter suggested
that we adopt the same methodology for
modeling charge increases and cost-tocharge ratio (CCR) changes in the IRF
PPS that we are currently using for IPPS
hospitals.
Response: As we noted in the FY 2008
IRF PPS final rule (72 FR 44284 at
44304), we considered adopting the
same methodology described in the FY
2007 IPPS final rule (71 FR 47870,
48150 though 48151) for projecting cost
and charge growth for IRFs. However,
we discovered that the accuracy of the
projections depends on the case mix of
patients in the facilities remaining
similar from year to year, as it does in
IPPS hospitals. As many of the
commenters on the FY 2009 IRF PPS
proposed rule noted, the case mix of
patients in IRFs was continuing to
change through at least the middle of FY
2008 in response to the 60 percent rule
and recent medical review activities. In
analyzing the data, we discovered that
we could get inaccurate results if we
based future projections of cost and
charge growth on data from years in
which IRFs were experiencing
fluctuations in case mix. Thus, since the
most recent available IRF claims data for
analysis in this final rule are the FY
2008 IRF claims data, and since we are
still seeing evidence of case mix
changes in these data, we do not believe
that adopting the suggested
methodology would be prudent at this
time. We believe that a better approach
would be to wait until the IRF case mix
has stabilized before we attempt to
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project cost and charge growth using the
suggested methodology. Otherwise, the
changes occurring in IRFs all at once,
including changes in IRFs’ charges,
costs, and case mix, could compromise
the accuracy of our results. For the
reasons described above, our analysis
shows that using the same methodology
we used previously for updating the
outlier threshold amount for FY 2010 is
the best approach at this time. However,
we will carefully consider the
commenter’s suggestions as we
investigate alternative approaches for
projecting IRF cost and charge growth in
estimating future updates to the IRF
outlier threshold amount.
Final Decision: Based on careful
consideration of the comments that we
received on the proposed update to the
outlier threshold amount for FY 2010
and based on updated analysis of the FY
2008 data, we are finalizing our decision
to update the outlier threshold amount
for FY 2010 to $10,652. In addition, we
did not receive any comments on the
IRF cost-to-charge ratio ceiling. Based
on our proposed policy and the reasons
set forth in the proposed rule (74 FR
21052, 21066 through 21067), we are
finalizing the national average urban
CCR at 0.494 and the national average
rural CCR at 0.622. We are also
finalizing our estimate of the IRF
national CCR ceiling at 1.61 for FY
2010.
VIII. Inpatient Rehabilitation Facility
(IRF) Coverage Requirements
In the FY 2010 proposed rule (74 FR
21052, 21067 through 21071), we
proposed IRF coverage requirements
and technical revisions to certain other
IRF requirements to reflect changes that
have occurred in medical practice
during the past 25 years and the
implementation of the IRF PPS. In light
of those proposals, we also proposed to
rescind the outdated HCFA Ruling 85–
2. We also noted that we anticipated
issuing new manual provisions to
provide further guidance on the
proposed rules if the changes were
ultimately finalized, and expressly
welcomed comments on the draft of
those manual provisions on our Web
site.
As we discussed in the proposed rule,
the policies that currently govern IRFs
were developed more than 25 years ago,
and were designed to provide coverage
criteria for a small subset of providers
furnishing intensive and complex
therapy services in a fee-for-service
environment to a small segment of
patients whose rehabilitation needs
could only be safely furnished at a
hospital level of care. In recognition of
the need to provide new coverage
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criteria, CMS assembled an internal
workgroup in June 2007 to determine
how best to clarify the criteria. The
workgroup enlisted the advice of
medical directors from within CMS,
from several of the fiscal intermediaries,
from one of the qualified independent
contractors (QICs), and from the
National Institutes of Health. These
individuals, including general
physicians, physiatrists, and therapists,
considered how best to identify those
patients for whom IRF coverage was
intended (that is, patients who both
require complex rehabilitation in a
hospital environment and could most
reasonably be expected to benefit from
IRF services). We also considered
comments that we received from
industry groups in response to the FY
2009 IRF PPS proposed rule (73 FR
22674) and in response to industry
input solicited by CMS contractors who
are preparing the IRF Report to Congress
mandated by section 115(c)(1) of the
Medicare, Medicaid, and SCHIP
Extension Act of 2007 (MMSEA), Public
Law 110–173.
After carefully considering all of the
input that we received from the
workgroup and from stakeholders, we
proposed a number of changes to the
regulation text in § 412.23 and § 412.29,
which were designed to clarify our
expectations regarding IRF coverage
criteria. We discussed our proposals and
suggested regulatory text to implement
those proposals.
Unfortunately, though we never
intended for these criteria to be used in
determining whether facilities could be
classified as IRFs, the combining of
§ 412.23 and § 412.29 and the placement
of the proposed IRF coverage
requirements in § 412.29, which
discusses the requirements for
rehabilitation units to be excluded from
the IPPS and instead be paid under the
IRF PPS, led several commenters to
incorrectly conclude that the proposed
coverage requirements would affect
classification of an IRF. This was not
our intent. To respond to these
comments and to eliminate confusion
on this point, we are creating a new
regulatory section at newly created
§ 412.622(a)(3), § 412.622(a)(4), and
§ 412.622(a)(5), in which we will place
the new IRF coverage requirements that
will be used to determine whether
individual IRF claims are for reasonable
and necessary services under section
1862(a)(1) of the Act. These new
coverage requirements will not be used
to determine whether a facility can be
paid under the IRF PPS. However,
certain of the requirements in the newly
created § 412.622(a)(3), § 412.622(a)(4),
and § 412.622(a)(5) mirror the concepts
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in the long-standing facility
classification requirements in the
existing § 412.23 and § 412.29, such as
the need to have a preadmission
screening process in place for all IRF
patients, the need to provide close
medical supervision by qualified
personnel, the need to have a plan of
treatment for all IRF patients, and the
need to use a ‘‘multidisciplinary’’
approach to care. In this final rule, we
will only make technical corrections to
those provisions governing facility
classification at § 412.23 and § 412.29 to
resolve any inconsistencies between the
new IRF coverage criteria applicable to
individual claims and the existing IRF
classification requirements. The facility
classification requirements at § 412.23
and § 412.29 will not be used to review
individual IRF claims. The details of the
regulatory changes that we are making
in this final rule are in the section
labeled ‘‘Final Decision’’ below.
We received 58 comments on our
overall approach to updating the IRF
coverage requirements, which are
summarized below.
Comment: Several commenters
supported our efforts to clarify the IRF
coverage criteria, with the Medicare
Payment Advisory Commission
(MedPAC) indicating that the new
criteria are a ‘‘positive step forward’’ in
providing a clearer set of expectations
and placing the focus more on patients’
functional needs. However, several
commenters expressed concerns about
the regulatory text that had been
proposed to implement these proposals,
and the authorities that we had cited in
the proposed rule. They especially
noted that, despite having proposed
coverage criteria, we had failed to
include section 1862 of the Act in our
list of authorities. Other commenters
suggested, due to a misunderstanding of
our statements about our intent to issue
manual guidance to implement the
proposed regulations once they were
finalized, that we had not met the
requirements of the Administrative
Procedure Act in our proposal to
rescind HCFAR 85–2.
Response: We believe the commenters
have misunderstood the approach that
we are using to make these updates to
the IRF coverage criteria. We are not
rescinding HCFAR 85–2 and replacing it
with revised manual provisions (in
Chapter 1, Section 110 of the MBPM).
Rather, we are using standard
rulemaking procedures to replace
HCFAR 85–2 with updated regulatory
provisions that contain the substantive
changes to the coverage criteria.
Consistent with the APA requirements,
we will rescind the prior standard
(HCFAR 85–2) in a future notice to be
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issued prior to implementation of the
new legal standards that are established
under this final rule. Once the updated
regulatory provisions are in effect, we
will issue revised manual provisions
that interpret the new regulatory
provisions. The revised manual
provisions will not contain substantive
requirements beyond those that are in
the regulations. We do, however, agree
that we should have included section
1862 of the Act in our list of authorities
in the proposed rule. We appreciate the
commenters bringing this inadvertent
omission to our attention. We have
corrected this omission in the
authorities list in this final rule.
Comment: Several commenters
expressed concerns that an IRF’s failure
to meet the proposed coverage criteria
would not only result in denial of an
individual claim, but would also
possibly result in a facility not being
eligible for classification as an IRF.
Some commenters questioned whether
we were, in effect, changing the ‘‘60
percent rule.’’ If so, they suggested that
CMS consider alternative ways of
amending the ‘‘60 percent rule’’ and
distinguishing IRFs from IPPS hospitals.
These commenters also suggested that
we clarify that the IRF classification
requirements are based on different
statutory authority than the IRF
coverage criteria and that the IRF
coverage criteria are not used to
determine IRF classifications.
Response: As noted above, we did not
intend for any of the proposed coverage
criteria to have any bearing on the
exclusion of facilities from the IPPS, the
requirements for the classification of
facilities as IRFs, or the 60 percent rule.
The proposed regulatory coverage
criteria were intended to update IRF
coverage criteria, not IRF classification
criteria. Unfortunately, the placement of
these draft coverage criteria in the
proposed regulatory text, especially in
concert with some words that were
inadvertently used in the preamble
discussion (we did, unfortunately, make
a reference to ‘‘exclusion’’ and
‘‘classification requirements’’ in our
discussion of the proposed coverage
criteria; however, we believe the
majority of the discussion conveys that
we were discussing coverage, not
classification) led many commenters to
incorrectly conclude that we were
proposing to make compliance with
coverage criteria a component of the IRF
classification requirements.
To eliminate any further confusion
regarding this point, we are creating
§ 412.622(a)(3), § 412.622(a)(4), and
§ 412.622(a)(5), which contain the new
coverage criteria regulations that are
adopted under this rule.
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Further, we agree with the
commenters that the IRF coverage
criteria and the IRF classification
requirements are different and are based
on different statutory authority. We also
agree that the IRF coverage criteria are
not used to determine IRF classification.
To be clear, in this final rule we are
adopting new regulatory IRF coverage
criteria. We do not intend for any IRF
to lose its classification status because
an individual patient does not meet the
IRF coverage criteria. Failure to meet the
coverage criteria in a particular case will
only result in the denial of the IRF’s
claim for the services provided to that
patient, not in a change in the
classification of the facility.
Comment: Several commenters
suggested that we delay implementation
of the new regulations and manual
instructions regarding the IRF medical
necessity criteria to give IRFs adequate
time to adapt their internal processes to
the changes. These commenters also
suggested that the additional time
would allow CMS to conduct training
on the changes, to hold provider
education conference calls similar to the
conference calls that we conducted in
2002 when the IRF PPS went into effect,
and to hold additional meetings with
stakeholders to further refine the
regulations.
Response: We believe that it is critical
to adopt regulatory IRF coverage criteria
as quickly as possible to provide clear
and updated rules that all stakeholders
can easily understand and follow.
However, we agree that a delay in the
implementation of the new regulations,
and the manual instructions that will be
issued to provide further guidance on
the substantive requirements contained
therein, until January 1, 2010 is
reasonable. This would allow IRFs more
time to adjust their internal processes
and procedures to accommodate the
new rules. The delayed implementation
would also allow time for CMS to
conduct thorough training and
education outreach on the new
regulations, which will benefit all
stakeholders by promoting a shared
understanding of the new regulations.
Although we understand the
commenters’ concerns about the need
for stakeholder input into these policies,
we have already incorporated
substantial input from the public in the
development of these policies. As we
noted in the FY 2010 proposed rule (74
FR 21052 at 21067), we received
substantial input from the public on the
medical necessity criteria from a town
hall meeting and Technical Expert Panel
that we conducted in February 2009 in
response to the mandated analysis of
IRF access and utilization issues
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contained in the Medicare, Medicaid,
and SCHIP Extension Act of 2007
(MMSEA), Public Law 110–173, section
155(c)(1). Even though the town hall
meeting and the Technical Expert Panel
were supposed to be focused on
developing alternatives to the criteria
for classifying an IRF, particularly
refinements to the 60 percent rule, in
many cases participants instead
provided CMS with information and
suggestions concerning the criteria for
establishing the medical necessity of
IRF admissions, which we considered in
the development of the proposed
updates to the regulation. In addition,
we received additional input from the
public in the comments that we
received on the FY 2010 IRF PPS
proposed rule. Thus, we do not believe
that it is necessary to conduct further
meetings prior to finalizing the
proposed regulations. However, we will
continue to conduct additional meetings
with stakeholders and provide training
and education to promote a shared
understanding of the new regulations.
We appreciate the suggestions regarding
the provider education conference calls
and plan to include these calls as part
of our training and public outreach on
these new regulations.
Comment: Several commenters
expressed concern that rescinding
HCFAR 85–2 prior to issuing manual
revisions would negatively affect IRF
claims denials that are currently being
reviewed by Administrative Law Judges
(ALJs).
Response: To alleviate the
commenters’ concerns, we will rescind
HCFAR 85–2 in a future notice that will
be issued prior to implementation of the
new regulatory provisions. We plan to
issue new manual guidance that will
interpret the new regulations at that
time as well. The new regulatory
provisions will become effective for IRF
discharges occurring on or after January
1, 2010. Thus, HCFAR 85–2 will
continue to apply for all IRF discharges
that occur prior to January 1, 2010. Once
the updated regulations become
effective, ALJs will be able to use the
new, clarified regulations. We believe
that simplifying and clarifying the rules
will make the rules easier for all
stakeholders, including ALJs, IRFs, and
Medicare contractors, to understand and
to follow. In so doing, we believe that
the updated regulations will reduce the
number of disputed IRF claims denials
that will be appealed to the ALJ level.
Comment: Several commenters
suggested that we provide the scientific
bases for the new regulations and a list
of the people with whom we consulted
in developing the new regulations.
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Response: As the new regulations are
intended merely to update and clarify
the prior IRF medical review policies,
we focused on updating the regulations
to reflect current industry practices that
we believe enhance the quality of care
for patients, not on establishing the
scientific basis for medical treatment.
We do not publish comprehensive
lists of the numerous employees who
participate in the collaborative policy
development process. We do, however,
indicate the names of the lead analysts.
Please see the section labeled ‘‘For
Further Information Contact’’ at the
beginning of this final rule for the
names and contact information of the
lead analysts on this rule. Please contact
the lead analysts for further information.
Comment: One commenter suggested
that we include all IRF medical
necessity requirements in both the
regulation text and the manual
instructions, so that the regulation text
and the manual instructions would both
be revised together through rulemaking.
Response: As we indicated above, we
are using standard rulemaking
procedures to implement regulatory
provisions governing the coverage
criteria for IRF services. Once the
regulatory provisions are finalized, we
will issue revised manual provisions
that provide detailed guidance on the
new regulatory provisions. As these
manual provisions will not contain
substantive requirements, there is no
need to promulgate the manual
provisions through the rulemaking
process. As noted in the proposed rule,
however, we solicited and carefully
considered comments on the draft
manual provisions submitted outside of
this APA rulemaking process.
Comment: One commenter suggested
that, given the complexity of the
proposed changes to the regulation, we
should provide for an additional 60-day
comment period to allow the public an
additional opportunity to comment on
the changes.
Response: We do not believe that the
proposed changes to the regulation were
extraordinarily complex, relative to the
regulations that we typically issue for
IRFs and other Medicare payment
systems. Thus, we believe that one 60day comment period was adequate to
provide for public comment on these
issues.
Comment: One commenter suggested
that we provide ‘‘justifiable exceptions’’
to all of the required timelines for the
preadmission screening, the postadmission physician evaluation, and the
overall individualized plan of care.
Response: We agree that there should
be exceptions to these timelines in the
case of extraordinary events, such as
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natural disasters or other states of
emergency, that are beyond the control
of the IRF. In such instances, we would
consider the appropriateness of using
established mechanisms for waiving or
modifying certain Medicare
requirements such as section 1135 of the
Act (under which the Secretary might
permit a temporary modification of the
timeline during the ‘‘emergency period’’
under section 1135 (g)(1) of the Act).
The preadmission screenings, postadmission physician evaluations, and
individualized overall plans of care are
part of an IRF’s standard operating
procedures. Thus, in non-emergency
situations, we expect that each IRF will
develop its own protocols to ensure
timely completion of these documents.
A. Requirements for the Preadmission
Screening
As discussed in the FY 2010 proposed
rule, we believe that a comprehensive
preadmission screening process is the
key factor in initially identifying
appropriate candidates for IRF care. For
this reason, we proposed to clarify our
expectations regarding the scope of the
preadmission assessment and to require
documentation of the clinical evaluation
process that forms the basis of the
admission decision.
In addition, to ensure that IRF
patients receive close medical
supervision, we proposed to require an
evaluation of each patient’s risk for
clinical and rehabilitation
complications as part of the
preadmission screening.
To capture the preadmission
screening information as close as
possible to the actual time of the IRF
admission, we proposed to require that
the preadmission screening be
conducted by qualified clinicians
designated by a rehabilitation physician
within the 48 hours immediately
preceding the IRF admission, and we
proposed to require that the
preadmission screening documentation
be retained in the patient’s medical
record.
We also proposed to require that a
rehabilitation physician review and
document his or her concurrence with
the findings and results of the
preadmission screening.
Finally, we proposed to eliminate the
3 to 10 day post-admission assessment,
which was used under the guidance
documents that predated the regulations
adopted under this rule for after-the-fact
proof of medical necessity.
We received 27 comments on the
proposed requirement for the
preadmission screening, which are
summarized below.
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Comment: While several commenters
expressed support for the proposed
preadmission screening requirement, a
few commenters said that the level of
detail that we are proposing for this
requirement exceeds what is typically
included in a preadmission screening.
One commenter indicated that acute
care hospital staff generally are not
trained to assess all of the components
of the patient’s condition that we
proposed to require be included in the
preadmission screening, and that the
level of evaluation that we are
suggesting is best performed by the
rehabilitation physician in the IRF.
Response: As noted in the FY 2010
proposed rule (74 FR 21052 at 21068),
we believe that a comprehensive
preadmission screening process is the
key factor in initially identifying
appropriate candidates for IRF care. As
we are placing more weight on the
rehabilitation physician’s decision to
admit the patient to the IRF, we believe
that it is important to require that the
rehabilitation physician document the
reasoning behind this decision, to
enable medical reviewers to understand
the rationale for the decision. We realize
that this level of detail may exceed what
some IRFs may have included in the
patient’s medical record in the past, but
we believe that it will benefit both the
IRFs and the Medicare contractors who
are reviewing IRF claims to have the
rationale for the reasoning behind the
admission decision recorded in each
patient’s medical record.
We agree that the assessment would
best be performed by the rehabilitation
physician or IRF clinical staff
designated by the rehabilitation
physician. We believe that the
commenter may have misunderstood
our proposal in that we do not expect
the acute care hospital staff to be
performing the preadmission screenings
for the IRF.
Comment: Several commenters
suggested that the clinical staff
performing the preadmission screenings
should be ‘‘qualified and competent,’’
but not ‘‘licensed,’’ because State
licensure laws differ and preadmission
screenings are generally not included in
clinicians’ scopes of practice. Several
commenters also suggested that we
allow non-clinical personnel to conduct
the preadmission screening, as is the
current practice in some IRFs. Further,
several commenters suggested that we
allow any licensed physician to review
and document his or her concurrence
with the results of the preadmission
screening.
Response: We disagree. Given the
complexity and the comprehensive
nature of the preadmission screenings
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that are required to determine the
appropriateness of an IRF admission, we
believe that a comprehensive
preadmission screening process is the
key factor in initially identifying
appropriate candidates for IRF care. As
such, we believe that the IRF personnel
involved in collecting the information
for the preadmission screening must be
appropriately trained and qualified to
assess the patient’s medical and
functional status, assess the risk for
clinical and rehabilitation
complications, and assess other aspects
of the patient’s condition both
medically and functionally. We do not
agree that non-clinical personnel can
adequately perform these assessments.
Further, we believe that only a licensed
rehabilitation physician with training
and experience in medical rehabilitation
should be making the IRF admission
decision.
Comment: Several commenters
expressed concerns that the requirement
for the preadmission screening to be
conducted within the 48 hours
immediately preceding the IRF
admission would preclude IRFs from
performing the preadmission screening
on the patients earlier in their acute care
hospital stay, as is the practice in some
IRFs. They suggested that we allow for
the possibility that IRFs could update
their preadmission screenings within
the 48 hours immediately preceding the
IRF admission and have this count
toward meeting the preadmission
screening requirement. One commenter
suggested that we require that the
preadmission screening be conducted
within the 96 hours immediately
preceding the IRF admission, rather
than 48 hours.
Response: We agree with the
commenters that the requirement as
proposed could preclude IRFs from
performing preadmission screenings on
patients earlier in their acute care
hospital stays, and we agree that
performing these preadmission
screenings earlier in the acute care
hospital stays could, in some cases, be
beneficial to the patients. For this
reason, we are changing the requirement
to allow for a comprehensive
preadmission screening that includes all
of the required elements to be
performed more than 48 hours
immediately preceding the IRF
admission, as long as an update is
conducted in person or by telephone
within 48 hours prior to the admission
and documented in the patient’s
medical record to update the patient’s
medical and functional status. To be
clear, a comprehensive preadmission
screening conducted entirely by
telephone without transmission of the
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patient’s acute care hospital records (if
the patient is being transferred from the
acute care hospital) and a review of
those records by licensed clinical staff
in the IRF is not acceptable. However,
if the comprehensive preadmission
screening is completed more than 48
hours prior to the IRF admission, the
required update within 48 hours of the
admission may be completed by
telephone.
We do not believe that permitting the
entire preadmission screening to be
conducted within the 96 hours
immediately preceding the IRF
admission, without the benefit of a more
recent update, would provide
sufficiently current information on the
patient’s medical and functional status
to allow the rehabilitation physician to
make an appropriate admission
decision.
Comment: Several commenters
expressed concerns about eliminating
the 3-day to 10-day inpatient assessment
period for determining whether an IRF
admission is appropriate, indicating that
IRFs often require several days after an
IRF admission to assess whether the
patient can participate in and benefit
from the intensive rehabilitation therapy
provided in IRFs.
Response: We disagree. The current
average length of stay for IRF patients is
only about 13 days, and the average
length of stay for many orthopedic
patients treated in IRFs is only about 8
days. Given this, we believe that it is no
longer appropriate to allow up to 10
days in an IRF merely to assess the
patient. At that point, the average IRF
patient would already be preparing to be
discharged.
In addition, we believe that, in today’s
clinical environment, licensed
physicians with training and experience
in rehabilitation are able to assess a
patient prior to admission to an IRF and
determine whether there is a reasonable
expectation that the patient can
participate in and benefit from
treatment in an IRF. In the unusual
instance that the rehabilitation
physician’s reasonable expectation prior
to admission is not realized once the
patient is admitted to the IRF, we are
allowing the IRF to begin making
arrangements to transfer the patient to
another setting of care and to receive the
short stay outlier payment for IRF stays
of 3 days or less (instead of having the
entire claim denied), as long as the
reasons for the change in the patient’s
status before and after admission are
well-documented in the patient’s
medical record.
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B. Requirement for a Post-Admission
Physician Evaluation
We proposed to add a requirement for
a post-admission evaluation by a
rehabilitation physician within 24 hours
of admission. The purpose of the
proposed post-admission evaluation
would be to document the patient’s
status on admission to the IRF, compare
it to that noted in the preadmission
screening documentation, and begin
development of the patient’s expected
course of treatment that would be
completed with input from all of the
interdisciplinary team members in the
overall plan of care. We also proposed
to require that this document be
retained in the patient’s medical record.
We received 21 comments on the
proposed requirement for a postadmission physician evaluation, which
are summarized below.
Comment: Several commenters
suggested that we allow the physician’s
history and physical (H&P) to satisfy the
requirement for the post-admission
physician evaluation.
Response: While the H&P is a
significant component of the admission
process, the post-admission evaluation
performed by the rehabilitation
physician is meant to include additional
information that goes beyond that
typically found in an H&P. Not only is
the post-admission evaluation intended
to provide a review of the medical
history of the patient and validate the
patient’s condition on admission, it also
provides guidance as to whether or not
it is safe to initiate the patient’s therapy
program and it supports the medical
necessity of the IRF admission. For
example, it would be useful for the postadmission physician evaluation to (1)
describe the clinical rehabilitation
complications for which the patient is at
risk, and the specific plan to avoid
them, (2) describe the adverse medical
conditions that might be created due to
the patient’s comorbidities and the
rigours of the intensive rehabilitation
program, and the methods that might be
used to avoid them, and (3) predict the
functional goals to be achieved within
the medical limitations of the patient.
As such, it is a combination medical/
functional resource for all team
members in the care of the patient as
they prepare to contribute to the
individualized overall plan of care.
Comment: Several commenters
suggested that other licensed
independent practitioners (LIPs), other
than the rehabilitation physician, be
allowed to complete the post-admission
evaluation.
Response: Although LIPs, in many
instances, complete H&Ps on IRF
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patients upon admission to the IRF in
order to write the medical orders, the
post-admission physician evaluation
requirements go beyond an H&P (as
discussed above). Thus, we believe that
the post-admission physician evaluation
requires the unique training and
experience of the rehabilitation
physician, as he or she performs a
hands-on evaluation of the patient.
Comment: Several commenters
expressed concerns that the postadmission physician evaluation would
be difficult to complete with input from
the interdisciplinary team within 24
hours of the patient’s admission to the
IRF, and that we should therefore
extend the requirement for completion
to either 36 hours or 3 days after the
patient’s admission to the IRF.
Additionally, one commenter suggested
that there is no need for a postadmission physician evaluation simply
to document that there have been no
changes in the patient since the
preadmission screening, and that the
post-admission evaluation would
therefore not be beneficial or costeffective.
Response: We agree with the
commenters that it may be difficult for
the rehabilitation physician to obtain
input from all of the interdisciplinary
team members in time to incorporate
this information into the post-admission
physician evaluation. For this reason,
we are removing the requirement that
the rehabilitation physician obtain input
from the interdisciplinary team in
completing the post-admission
physician evaluation. However, we
continue to believe that it would be in
the best interest of the patient for the
rehabilitation physician to consider any
input that is available from the
interdisciplinary team members in
completing the post-admission
physician evaluation.
As we indicated in the FY 2010
proposed rule (74 FR 21052 at 21070),
we believe that rehabilitation therapy
services should begin as soon as
possible after a patient is admitted to an
IRF, thereby increasing the patient’s
potential for achieving functional goals.
For this reason, we believe that it is
necessary for a patient to be seen by a
rehabilitation physician within 24 hours
of the patient’s admission. Therefore,
we disagree that the post-admission
physician evaluation should be allowed
to occur 36 hours or 3 days later. If there
are no changes in the patient since the
preadmission screening, then the
patient’s condition should be relatively
easy for the rehabilitation physician to
document. However, if there have been
changes in the patient’s medical or
functional status, or any other changes
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in the patient’s condition or status, from
that noted in the preadmission
screening, documentation of these
changes and the reasons for these
changes is important in determining the
continued appropriateness of the IRF
admission.
Comment: One commenter asked for
clarification regarding whether the postadmission physician evaluation
requirement affects the IRF–PAI
assessment reference date or the
requirements for completing the IRF–
PAI. Specifically, the commenter asked
whether the IRF–PAI must now be
completed prior to the patient’s
admission to the IRF.
Response: The post-admission
physician evaluation requirement does
not affect the IRF–PAI assessment
reference date or the requirements for
completing the IRF–PAI (as described in
§ 412.610(a)(1)). The IRF–PAI cannot be
completed prior to the patient’s
admission to the IRF. The IRF–PAI must
be completed by the end of the fourth
day after the patient’s admission to the
IRF, and should be based on
information obtained during the first 3
days following the IRF admission.
C. Requirement for an Individualized
Overall Plan of Care
The overall plan of care is essential to
providing high-quality care in IRFs.
Comprehensive planning of the patient’s
course of treatment in the early stages of
the IRF stay leads to a more coordinated
delivery of services to the patient, and
such coordinated care is a critical aspect
of the care provided in IRFs. Thus, we
proposed to require that an
individualized overall plan of care be
developed for each IRF admission by a
rehabilitation physician with input from
the interdisciplinary team within 72
hours of the patient’s admission to the
IRF, and be retained in the patient’s
medical record.
We received 17 comments on the
proposed requirement for an
individualized overall plan of care,
which are summarized below.
Comment: Several commenters
suggested that requiring the
individualized overall plan of care to be
completed within 72 hours of the
patient’s admission to the IRF was
unrealistic, especially given that IRFs
are required to complete the IRF patient
assessment instruments (IRF–PAIs) for
each patient by the end of the patient’s
fourth day in the IRF. Several
commenters suggested alternative
requirements, such as adopting the same
timing for the individualized overall
plan of care that we require for
completing the IRF–PAI (as described in
§ 412.610(a)(1)), extending the period of
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time for completing the overall plan of
care to 96 hours and requiring it to be
finalized at the first interdisciplinary
team meeting, and requiring the overall
plan of care to be finalized within the
first 5 days of admission.
Response: We agree that requiring the
individualized overall plan of care to be
completed by the end of the fourth day
following the patient’s admission to the
IRF would allow all of the information
from the IRF–PAI to be incorporated
into the patient’s overall plan of care,
thereby enriching the patient’s overall
plan of care. Thus, we are adopting the
timeline suggested by several of the
commenters and are requiring that the
overall plan of care be completed by the
end of the fourth day following the
patient’s admission to the IRF. We
believe that the commenters’
suggestions for longer timeframes would
unnecessarily delay the initiation of
treatment in the IRF and would,
thereby, limit patients’ potential for
achieving functional outcomes.
Comment: Several commenters
suggested that we require the first
interdisciplinary team meeting to be
conducted within the first 4 days
following the patient’s admission to the
IRF to develop the individualized
overall plan of care and to adequately
reflect the importance of the
contributions of the interdisciplinary
team to the care planning process.
Response: Although we believe that
conducting the first interdisciplinary
team meeting for each IRF patient
within the first 4 days of admission to
develop the overall plan of care would
be a good practice in IRFs, we do not
believe that a team meeting is the only
way to develop an overall plan of care.
As long as all of the required elements
for the overall plan of care are present
in the patient’s medical record, we
believe that it should be left up to each
individual IRF to determine the best
method for developing the patient’s
overall plan of care.
Comment: One commenter suggested
that we provide examples of overall
individualized plans of care for patients
with specific conditions.
Response: We believe that it is
important to note that the overall plan
of care for each IRF patient should be
individualized to that patient’s unique
care needs. Thus, we do not believe that
it is appropriate to provide such
examples.
D. Requirements for Evaluating the
Appropriateness of an IRF Admission
In the FY 2010 proposed rule (74 FR
21052 at 21069), we also proposed to
require that the comprehensive
preadmission screening include an
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evaluation of the following proposed
requirements that a patient must meet to
be admitted to an IRF:
1. Whether the patient’s condition is
sufficiently stable to allow the patient to
actively participate in an intensive
rehabilitation program.
2. Whether the patient has the
appropriate therapy needs for placement
in an IRF, meaning that the patient
requires the active and ongoing
therapeutic intervention of at least two
therapy disciplines (physical therapy,
occupational therapy, speech-language
pathology, or prosthetics/orthotics
therapy), one of which must be physical
or occupational therapy.
3. Whether the patient requires the
intensive services of an inpatient
rehabilitation setting, which is typically
measured by whether the patient
generally requires and can reasonably be
expected to actively participate in at
least 3 hours of therapy per day at least
5 days per week, and be expected to
make measurable improvement that will
be of practical value to improve the
patient’s functional capacity or
adaptation to impairments.
We received 58 comments on the
proposed requirements for evaluating
the appropriateness of an IRF
admission, which are summarized
below.
Comment: Several commenters
suggested that we further define what
we mean by a patient’s condition being
‘‘sufficiently stable’’ to actively
participate in an intensive rehabilitation
program. Many of these commenters
expressed concerns that we may not be
adequately recognizing that IRFs
provide an inpatient level of care,
similar to that provided in acute care
hospitals. In addition, one commenter
expressed the concern that the new
regulations would mean that patients
would have to remain in the acute care
hospital longer until their conditions
stabilized, which would delay the
initiation of therapy services. Another
commenter expressed the concern that
the new regulations would
inappropriately penalize IRFs for
fluctuations in a patient’s condition.
One commenter suggested that we
revise the regulation to require that a
patient’s condition be sufficiently stable
‘‘at the time that rehabilitation services
are provided,’’ while another
commenter suggested that we require
that all services that are considered part
of the acute care hospital’s Medical
Severity-Diagnostic Related Group (MS–
DRG) payment bundle be completed
prior to transfer to the IRF. A third
commenter suggested that the
determining factor of medical stability
should be whether the patient can
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participate in the intensive
rehabilitation therapy program provided
in an IRF, at the same time that the IRF
manages the patient’s medical issues.
Response: We agree with the
commenters that IRFs provide a
hospital-level of care, with a focus on
providing post-acute rehabilitation
therapy services. However, we do not
believe that patients should be
transferred to IRFs before their medical
conditions are sufficiently stable to
enable them to participate in the
intensive rehabilitation therapy program
provided in IRFs. Specifically, we mean
that, at the time of admission to the IRF,
there must be a reasonable expectation
that the patient is able to tolerate and
benefit from the intensive rehabilitation
services as generally prescribed in this
rule so that he or she can progressively
make the improvements needed to
achieve results of practical value
towards his or her functional capacity or
adaptation to impairment. However, we
note that this does not mean that
patients’ medical conditions will be
fully resolved when they are admitted to
IRFs. As one of the commenters
summarized, we are requiring that a
patient’s medical condition be such that
it can be successfully managed in the
IRF setting at the same time that the
patient is participating in the intensive
rehabilitation therapy program provided
in an IRF.
Comment: Several commenters
expressed concerns that we would be
imposing too high a standard in
requiring the IRF to demonstrate that
each patient it admits meets the IRF
coverage criteria ‘‘at the time of
admission.’’ The commenters suggested,
instead, that we require the IRF to
demonstrate a reasonable expectation at
the time of admission that the patients
would meet the IRF coverage criteria.
Alternatively, several commenters
suggested that we instead require that
the patient meet the IRF coverage
criteria by the assessment reference date
for the IRF–PAI (that is, by the fourth
day following admission to the IRF) or
by the time that therapy is initiated.
Response: We agree with several of
the commenters that a reasonable
expectation that the patient meets the
IRF coverage criteria at the time of
admission is sufficient, and are
therefore clarifying the language to read,
‘‘The facility must ensure that there is
a reasonable expectation that each
patient it admits meets the following
requirements at the time of
admission—.’’ This language better
reflects our intention in proposing this
policy. We note that the detailed
reasoning behind this reasonable
expectation must be documented in the
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preadmission screening, and that it
must be supported by the information in
the post-admission physician evaluation
and the overall individualized plan of
care. We do not believe that it is
appropriate to provide 4 days (at which
point the IRF would generally receive a
full CMG payment for the patient) or an
undefined amount of time for the IRF to
determine whether the patient meets the
IRF medical necessity criteria. This
determination should be made at the
time of admission to the IRF.
Comment: Several commenters
expressed concerns that the ‘‘3-hour
rule’’ could preclude access to IRF care
for certain patients who, for one reason
or another, cannot participate in at least
3 hours of intensive therapy at least 5
days per week, but who nonetheless
could benefit from treatment in an IRF.
Several of these commenters suggested
that this rule would violate Hooper v.
Sullivan, No H–80–99 (PCD) (D Conn.
July 20, 1989). For this reason, some
commenters suggested that we allow
exceptions to this rule for patients who
need other rehabilitation services, but
cannot tolerate 3 hours per day of
physical therapy, occupational therapy,
speech-language pathology, or
prosthetics/orthotics therapy. Some
commenters also suggested that we
allow for exceptions to this rule for
patients who require a lower intensity of
therapy services but for whom an IRF
admission is the only way that they can
participate in a lower intensity of
therapy services. In addition, one of the
commenters suggested that, in some
cases, we should provide more
flexibility for meeting the needs of the
individual patient by requiring instead
that the IRF provide intensive therapy at
least 15 hours per week, to be averaged
over the week as necessary.
Response: We believe that patients
admitted to IRFs should generally
require and be reasonably expected to
benefit from the intensive rehabilitation
therapy services that are uniquely
provided in IRFs. If patients do not need
the intensity of services uniquely
provided in IRFs, or benefit from them,
then it is not clear to us why they would
be admitted to an IRF.
By order of the Court in Hooper v.
Sullivan, rules of thumb cannot serve as
the basis of a coverage denial. In
keeping with this ruling, the reasonable
and necessary test for coverage of an IRF
stay is whether the patient received, and
could be expected to benefit from,
‘‘intensive rehabilitation services.’’
Please refer to section 110 of the
Medicare Benefit Policy Manual, once
the revisions that we anticipate issuing
on January 1, 2010 have been published,
for more specific guidance on what type
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of information to include when
documenting an individualized overall
plan of care. Although the intensity of
rehabilitation services can be reflected
in various ways, the generally-accepted
standard by which the intensity of these
services is typically demonstrated in
IRFs is by the provision of intensive
therapies at least 3 hours per day at least
5 days per week. However, we do not
intend for this to be the only way such
intensity can be demonstrated (that is,
we do not intend for this measure to be
used as a ‘‘rule of thumb’’ for denying
an IRF claim). Rather, we suggest that
this is one generally accepted way of
demonstrating the intensity of services
provided in an IRF.
We agree with several of the
commenters that the intensity of therapy
provided in IRFs could also be
demonstrated by the provision of 15
hours of therapy per week (that is, in a
7-consecutive day period starting from
the date of admission). For example, if
a hypothetical IRF patient was admitted
to an IRF for a hip fracture, but was also
undergoing chemotherapy for an
unrelated issue, the patient might not be
able to tolerate therapy on a predictable
basis due to the chemotherapy. Thus,
this hypothetical patient might be more
effectively served by the provision of 4
hours of therapy 3 days per week and
11⁄2 hours of therapy on 2 (or more)
other days per week in order to
accommodate his or her chemotherapy
schedule. Thus, IRFs may also
demonstrate a patient’s need for
intensive rehabilitation therapy services
by showing that the patient required
and could reasonably be expected to
benefit from at least 15 hours of therapy
per week (defined as a 7 consecutive
day period starting from the date of
admission), as long as the reasons for
the patient’s periodic need for this
program of intensive rehabilitation is
well-documented in the patient’s
medical record and the overall amount
of therapy is ‘‘intensive’’ and can
reasonably be expected to benefit the
patient. We will monitor the
appropriateness of instances where IRFs
demonstrate the required level of
intensity in this way.
In addition, we note that we will
provide guidance in our manuals on
additional instances in which we might
find that the patient is receiving
intensive rehabilitation therapy services
despite not receiving the generally
expected intensity of therapy services
for a brief period of time.
Comment: Several commenters
suggested that we include other
services, such as recreational therapy,
music therapy, respiratory therapy,
psychology, and neuropsychology, on
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the list of therapy services that IRFs
must provide, as needed, under
§ 412.23(b)(4) and § 412.29(c). These
commenters also suggested that we
specify in the new requirements
whether ‘‘other rehabilitative services,’’
such as recreational therapy, music
therapy, or respiratory therapy, can be
used to meet the intensity of therapy
requirements, if they are medical
necessary and ordered by a physician.
Response: While we believe that IRFs
should provide, as needed,
psychological and neuropsychological
services to IRF patients, these services
are separately billable under Medicare
Part B, as described in § 411.15(m)(3)(i)
and § 411.15(m)(3)(v), and are not
included in the IRF PPS payment. Thus,
while we would expect the IRF to
provide appropriate medical oversight
of any medical or psychiatric problem
that is present on admission or develops
during the stay (in accordance with the
overall hospital Conditions of
Participation at § 482.12(c)(1)(i),
(c)(1)(vi), and (c)(4)), psychological and
neuropsychological services furnished
pursuant to this responsibility would
not be considered part of the required
intensity of therapy services that
Medicare pays for under the Part A
benefit that includes payment for IRF
PPS services.
Further, we do not believe that it is
appropriate to mandate that all IRFs
provide recreational therapy, music
therapy, or respiratory therapy services
to all IRF patients, as such services may
be beneficial to some, but not all,
patients as an adjunct to other, primary
types of therapy services provided in an
IRF (physical therapy, occupational
therapy, speech-language pathology,
and prosthetics/orthotics therapy).
However, we do not believe that they
should replace the provision of these
four core skilled therapy services. Thus,
we believe that it should be left to each
individual IRF to determine whether
offering recreational therapy, music
therapy, or respiratory therapy is the
best way to achieve the desired patient
care outcomes. While we are not adding
these therapies to the list of required
therapy services in IRFs, we do
recognize that they are Medicarecovered services in IRFs if the medical
necessity is well documented by the
rehabilitation physician in the medical
record and is ordered by the
rehabilitation physician as part of the
overall plan of care for the patient.
However, consistent with our longstanding policies and standard
practices, these therapy activities are
not used to demonstrate that a patient
has received intensive therapy services.
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Comment: Several commenters
indicated that the term ‘‘of practical
value to the patient’’ when referring to
the level of functional improvement that
a patient may be expected to attain in
an IRF is subjective, and suggested that
we address improvement in the
patient’s ‘‘quality of life’’ instead.
Response: We believe that it will
generally be apparent from the
documentation by the rehabilitation
physician whether there is a reasonable
expectation that a particular functional
improvement or adaptation to
impairment will be of practical value to
the patient, within the context of his or
her individual situation. Quality of life,
a more global term, is influenced by
many factors that are unique to the
patient, but which may or may not be
able to be fully addressed during an IRF
stay.
E. Requirements for the
Interdisciplinary Team Meetings
Since an interdisciplinary approach to
care is such a hallmark of the care
provided in the IRF setting, we
proposed to modify the terminology that
we use throughout the IRF requirements
to specify an ‘‘interdisciplinary’’
approach to care rather than a
‘‘multidisciplinary’’ approach. Further,
since the length of many IRF stays has
decreased significantly in recent years,
we proposed to require that the
interdisciplinary team meetings occur at
least once per week throughout each IRF
stay (instead of at least once every two
weeks, as the previous regulations
stated).
Also, to improve the effectiveness and
coordination of the care provided to IRF
patients and to better reflect best
practices in IRFs, we proposed to
broaden the requirements regarding the
professional personnel that are expected
to participate in the interdisciplinary
team meetings. We proposed that, at a
minimum, the interdisciplinary team
must consist of professionals from the
following disciplines (each of whom
must have current knowledge of the
beneficiary as documented in the
medical record):
• A rehabilitation physician with
specialized training and experience in
rehabilitation services;
• A registered nurse with specialized
training or experience in rehabilitation;
• A social worker or a case manager
(or both); and
• A licensed or certified therapist
from each therapy discipline involved
in treating the patient.
Although the purpose of the proposed
requirement for interdisciplinary team
meetings is to allow the exchange of
information from all of the different
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disciplines involved in the patient’s
care, we indicated in the proposed rule
that we believe that it is important to
designate one person, specifically the
rehabilitation physician, to be
responsible for making the final
decisions regarding the patient’s IRF
care. Thus, we proposed to require that
the rehabilitation physician document
concurrence with all decisions made by
the interdisciplinary team at each
meeting.
As discussed above, we also proposed
to require that the interdisciplinary
team include registered nurses with
specialized training or experience in
rehabilitation. However, we proposed to
eliminate the requirement that IRFs
demonstrate that the patients need 24hour rehabilitation nursing care because
we believe that the patient’s need for
this care would already be identified by
the clinical risk factors documented in
the patient’s medical record. However,
as discussed below, several of the
commenters misinterpreted our
proposed elimination of this admission
criterion as an indication that CMS was
no longer valuing rehabilitation nursing
in IRFs. We emphasize that it was not
our intention to diminish the value of
rehabilitation nursing in IRFs; we
merely believe that this requirement
should be a facility requirement rather
than an IRF admission criterion.
We received 10 comments on the
proposed requirements for the
interdisciplinary team meetings, which
are summarized below.
Comment: The majority of
commenters agreed that weekly
interdisciplinary team meetings were
the standard of care in IRFs today, and
therefore supported this policy.
However, one commenter suggested that
this requirement would remove the
flexibility and individualization in IRFs.
This commenter indicated that
communication among disciplines in an
IRF is ongoing and often informal, and
that the requirement for a representative
of every treating discipline to be present
at every team meeting is excessive. The
commenter suggested that the presence
of one appointed therapist with
knowledge of the patient’s progress
would be sufficient for the team
meeting.
Response: As discussed in the FY
2010 proposed rule (74 FR 21052 at
21070), the purpose of the
interdisciplinary team meeting is to
foster communication among
disciplines to establish, prioritize, and
achieve treatment goals. Though we
agree that informal communications
among the disciplines on a daily basis
are beneficial for the patient, we believe
that it is important to require that all
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treating disciplines meet formally at
least once per week to maximize the
patient’s potential for meeting the
treatment goals.
Comment: Several commenters
expressed concerns about the removal of
the 24-hour rehabilitation nursing
requirement from the IRF coverage
criteria, indicating that we were not
sufficiently recognizing the value of
rehabilitation nursing in IRFs.
Response: As discussed above, we
proposed to require that the
interdisciplinary team include
registered nurses with specialized
training or experience in rehabilitation.
However, we proposed to eliminate this
as a coverage criterion because we
believe that this criterion should be a
facility-level requirement rather than a
patient admission criterion. As a
coverage criterion, the patient’s need for
this care would already be identified by
the clinical risk factors documented in
the patient’s medical record.
Comment: One commenter asked for
clarification regarding whether the first
team conference would be required to
be conducted within the first 72 hours
of the patient’s admission to the IRF in
order to develop the overall
individualized plan of care, or whether
it would be required to be conducted
within the first four days of admission
to correspond with the completion of
the IRF–PAI.
Response: We are merely requiring
the first team conference to occur within
the first week of the patient’s admission
to the IRF. While we believe that it may
be good practice to conduct the first
team meeting within the first 4 days to
develop the overall individualized plan
of care, we believe that there may be
other ways of developing the overall
individualized plan of care, and we
believe that IRFs should have the
flexibility to develop this
documentation using whatever internal
processes they believe are most
appropriate.
F. Requirement for Physician
Supervision
One of the primary reasons for a
patient to receive rehabilitation therapy
services in an inpatient hospital (that is,
IRF) setting is that the patient’s medical
conditions require close medical
supervision. In the past, the definition
of close medical supervision has been
vague. During the past 25 years, it was
often assumed that ‘‘close medical
supervision’’ was demonstrated by
frequent changes in orders due to a
patient’s fluctuating medical status.
Currently, however, patients’ medical
conditions can be more effectively
managed so that they are less likely to
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fluctuate and interfere with the rigorous
program of therapies provided in an
IRF.
In addition, the medical complexity of
rehabilitation patients has increased
over time and they often require the
services of multiple physicians to
manage their medical conditions and
ensure that they are able to maximize
their rehabilitation potential in the IRF.
Therefore, while multiple specialists
may visit the patient at the IRF, we
believe that it is the unique
responsibility of the rehabilitation
physician to coordinate the patient’s
medical needs with his or her functional
rehabilitation needs while in the
facility. Thus, we proposed to require
that a rehabilitation physician conduct
face-to-face visits with the patient at
least 3 days per week throughout the
patient’s IRF stay to assess the patient
both medically and functionally, as well
as to modify the course of treatment as
needed to maximize the patient’s
capacity to benefit from the intensive
rehabilitation program provided in the
IRF.
We received 7 comments on the
proposed requirement for physician
supervision, which are summarized
below.
Comment: Several commenters stated
that the requirement for a minimum of
3 face-to-face visits with the
rehabilitation physician per week was
reasonable. However, several
commenters noted further that a
reasonable standard of care would
require physicians to see an IRF patient
on a more frequent basis.
Response: We believe that each
patient in an IRF requires an
individualized standard of care. We also
acknowledge that each IRF can develop
its own standards as to what specialists
are available to provide medical services
to its patients and the frequency of their
visitation that supports patient safety.
However, our proposal refers only to our
belief that a rehabilitation physician is
that professional who is uniquely
qualified to assess all aspects of the
patient’s medical condition (with input
from others as needed) and apply this
knowledge to modify or advance the
program of therapies that the patient is
receiving in the IRF to provide for a
desirable functional outcome. We
believe that consideration or
reassessment of the patient’s functional
goals at least 3 times per week by the
rehabilitation physician and his or her
documentation of these visits in the
medical record is the minimum
standard that should be applied in an
IRF. All IRFs may increase the
frequency of the physician visits as they
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believe best serves their patient
populations.
G. Requirement Regarding Initiation of
Therapy Services
In addition to the proposed regulatory
changes discussed above, we proposed
to require that the required therapy
treatments begin within 36 hours after
the patient’s admission to the IRF.
We received 9 comments on the
proposed requirement regarding the
initiation of therapy services, which are
summarized below.
Comment: Several commenters
expressed concerns about the
requirement that therapies be initiated
within 36 hours of admission to the IRF.
They indicated that this would require
therapies to be initiated by 4 a.m. on
Sunday for patients admitted to the IRF
at 4 p.m. on Friday, and that this would
be unrealistic. They also indicated that
therapy staff generally do not treat
patients on weekends, and that this
provision would create staffing
problems for IRFs. For this reason, the
commenters suggested that we either
leave it to the physician’s judgment to
determine when therapy treatments
should begin, require therapy to be
initiated within a ‘‘reasonable period of
time’’ from admission to the IRF, or
require that therapy be initiated within
36 or 48 hours from midnight of the day
of admission.
Response: IRFs are a specialized type
of hospital and, like acute care
hospitals, are supposed to provide
services 7 days a week. Therefore, just
as we do not believe that patients who
are admitted to acute care hospitals on
Friday should have to wait until
Monday to have their acute care needs
met, we also do not believe that IRF
patients who are admitted to IRFs on
Friday should have to wait until
Monday to have their rehabilitation
therapy needs met. Given that the
average length of stay in IRFs is only
about 13 days, and that the average
length of stay for certain orthopedic
patients is only about 8 days, we believe
that it would be unreasonable for an IRF
not to provide rehabilitation therapies to
patients on the weekend, as this would
mean that patients would not be
participating in therapies for a
significant portion of their stay in the
IRF. Further, since patients’ potential
for functional recovery often depends
on initiating rehabilitation therapies as
early as possible, we believe that it is
essential that IRFs provide
rehabilitation therapy on weekends to
ensure that patients are able to
maximize their functional goals.
Thus, our intent is to require IRFs to
initiate rehabilitation therapies as soon
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as possible after admission to the IRF.
We had proposed to require that IRFs
initiate therapy no later than 36 hours
after a patient’s admission to the IRF.
However, some commenters suggested
that this would mean that patients
admitted to IRFs at 4 p.m. on Friday
would need to being therapy by 4 a.m.
on Sunday, and that this would
effectively require IRFs to begin
therapies on Saturday. As it was not our
intention to be this restrictive, we are
instead requiring that IRFs initiate
therapies for all patients within 36
hours from midnight of the day of
admission. So, for example, a
hypothetical patient admitted to the IRF
at 4 p.m. on Friday would need to begin
therapies by noon on Sunday.
Comment: Several commenters
suggested that we specify whether
therapy evaluations would satisfy the
requirement for the initiation of therapy.
Response: Therapy evaluations would
satisfy the requirement for therapy to be
initiated within 36 hours from midnight
of the day of admission.
H. Provision of Group Therapies in IRFs
As we discussed in the FY 2010
proposed rule (74 FR 21052, 21070
through 21071), another critical aspect
of IRF care is that rehabilitation therapy
services are generally provided to each
patient by a licensed or certified
therapist working directly with the
patient, more commonly known as oneon-one therapy. It has come to our
attention that some IRFs are providing
essentially all ‘‘group therapy’’ to their
patients. We believe that group
therapies may have a role in patient care
in an IRF, but that they should be used
in IRFs primarily as an adjunct to oneon-one therapy services which should
be the standard of care in therapy
service provided to IRF patients. We
believe that group therapy should be
considered as a supplement to the
intensive individual therapy services
generally provided in an IRF. To
improve our understanding of when
group therapy may be appropriate in
IRFs, we specifically solicited
comments on the types of patients for
which group therapy may be
appropriate, and the specific amounts of
group therapies instead of one-on-one
therapies that may be beneficial for
these types of patients. We stated that
we anticipated using this information to
assess the appropriate use of group
therapies in IRFs and that we might
create standards for group therapies in
IRFs.
We received 32 comments regarding
our request for comments on the types
of patients for which group therapy may
be appropriate, and the specific
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amounts of group instead of one-on-one
therapies that may be beneficial for
these types of patients.
Comment: A majority of the
commenters stated that group therapies
do have an important role in the
provision of therapies in IRFs, but they
also suggested that the amount of group
therapies provided in IRFs should be
limited in some way. Many commenters
agreed that group therapies are a good
adjunct to one-on-one therapies, but
should not be the primary source of
therapy services provided in IRFs.
Several commenters suggested that the
size of the groups should not exceed 2
to 4 patients for every one licensed
therapist, and that the groups should be
comprised of patients with similar
diagnoses. Commenters generally
suggested that we conduct further
research and consult with experts before
proposing standards for the provision of
group therapies in IRFs.
Response: As we have stated, the
standard of care for IRF patients is
individualized therapy. Group therapies
serve as an adjunct to individual
therapies. In those instances in which
group therapy better meets the patient’s
needs on a limited basis, the situation/
rationale that justifies group therapy
should be specified in the patient’s
medical record. We plan to consider the
adoption of specific standards on the
use of group therapies at a future date.
We appreciate the information that the
commenters provided.
I. Clarifying and Conforming
Amendments
In the FY 2010 proposed rule (74 FR
21052, 21080 through 21081), we
proposed revisions to § 412.23 and
§ 412.29 to combine the facility
classification requirements for
rehabilitation hospitals and
rehabilitation units of acute care
hospitals into one section at § 412.29,
and to add the new coverage
requirements to § 412.29. However,
upon reviewing the comments that we
received on the proposed rule, we
realized that combining the
requirements for hospital-based and
freestanding IRFs into one section, and
including coverage requirements in that
same section, resulted in some
confusion about whether and to what
extent the facility requirements were
being altered, and whether we were
making coverage criteria a classification
requirement. To eliminate this
confusion, we are retaining the separate
sections at § 412.23 and § 412.29
(governing facility requirements for
rehabilitation hospitals and
rehabilitation units, respectively) and
making conforming changes to these
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two sections to mirror the new coverage
criteria, which appear in the new
sections § 412.622(a)(3), § 412.622(a)(4),
and § 412.622(a)(5). However, the
facility criteria requirements, as
modified, will be retained in § 412.23
and § 412.29. These facility criteria will
not be used to determine whether
individual IRF claims are for services
that are reasonable and necessary under
section 1862(a)(1) of the Act. The
conforming changes, which we are
making to the identical text in both
§ 412.23 and § 412.29 are:
• To remove the words ‘‘or
assessment’’ from § 412.23(b)(3) and
§ 412.29(b) to indicate that we are no
longer providing for a 3 to 10 day
inpatient assessment period after
admission to assess the appropriateness
of the IRF admission, as discussed
above.
• To amend paragraphs § 412.23(b)(4)
and § 412.29(c) to require that IRFs
‘‘furnish, through the use of qualified
personnel, rehabilitation nursing,
physical therapy, and occupational
therapy, plus, as needed, speechlanguage pathology, social services,
psychological services (including
neuropsychological services), and
orthotic and prosthetic services.’’ This
amendment is in response to comments,
as discussed above. To replace the word
‘‘multidisciplinary’’ with the word
‘‘interdisciplinary’’ in § 412.23(b)(7) and
§ 412.29(e) to make the terminology
consistent with the new IRF coverage
criteria in the newly created
§ 412.622(a)(3), § 412.622(a)(4), and
§ 412.622(a)(5). To require, in both
§ 412.23(b)(7) and § 412.29(e), that the
interdisciplinary team meetings occur at
least once per week to be consistent
with the new IRF coverage criteria in
the newly created § 412.622(a)(3),
§ 412.622(a)(4), and § 412.622(a)(5).
To eliminate any further confusion
about whether we are promulgating new
IRF coverage requirements or new
facility classification requirements in
this final rule, we are withdrawing all
other proposed changes to § 412.23 and
§ 412.29 at this time.
J. HCFAR 85–2 Ruling
As noted previously, the HCFAR is
outdated and inconsistent with the IRF
PPS. The adoption of the proposed
coverage criteria would establish a new
legal framework. These new regulatory
requirements would not mirror the
provisions in HCFAR 85–2. Therefore,
to prevent further confusion over which
document provides instructions on the
IRF PPS regulations, we proposed that
HCFAR 85–2 would be rescinded and
new manual provisions offering
guidance on the new regulatory
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39797
coverage criteria would be issued. In
light of the adoption of a new regulatory
framework under this final rule, it is
appropriate to rescind HCFAR 85–2. We
now realize, however, that the
rescission needs to be done through
issuance of a notice in the Federal
Register. Thus, we will issue a notice in
the Federal Register at a future date to
notify the public of the rescission of
HCFAR 85–2, effective for IRF
discharges occurring on or after January
1, 2010. We anticipate that the new
regulatory requirements that are
adopted by this rule, once implemented,
will be further interpreted by new
manual provisions that will be placed in
Chapter 1, Section 110 of the MBPM.
We received 14 comments on the
proposed rescission of HCFAR 85–2,
which are summarized below.
Comment: Several commenters
expressed concern that rescinding
HCFAR 85–2 prior to issuing manual
revisions would negatively affect IRF
claims denials that are currently being
reviewed by ALJs.
Response: We will rescind HCFAR
85–2 in a future notice issued in the
Federal Register prior to the
implementation of the new regulatory
provisions. We anticipate issuing
manual guidance that will interpret the
new regulations. The new regulatory
provisions will become effective for IRF
discharges occurring on or after January
1, 2010. Thus, as we will discuss in a
future notice to be issued in the Federal
Register, HCFAR 85–2 will continue to
apply for all IRF discharges that occur
prior to January 1, 2010. Once the
updated regulations become effective,
ALJs will be able to use the new,
clarified regulations. We believe that
simplifying and clarifying the rules will
make the rules easier for all
stakeholders, including ALJs, IRFs, and
Medicare contractors, to understand and
to follow. In so doing, we believe that
the updated regulations will reduce the
number of disputed IRF claims denials
that will be appealed to the ALJ level.
Final Decision: After carefully
considering all of the comments we
received on the proposed updates to the
IRF coverage requirements, we are
finalizing the regulation text changes as
proposed, except for the revisions in
response to comment indicated below.
In addition, to eliminate any confusion
that these coverage requirements are
requirements for determining whether
an IRF claim meets the reasonable and
necessary provision of the statute rather
than facility classification requirements,
we are moving these coverage
requirements to a newly created
§ 412.622(a)(3), § 412.622(a)(4), and
§ 412.622(a)(5). Finally, we will rescind
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HCFAR 85–2 in a future notice to be
issued in the Federal Register.
We are adding requirements to
§ 412.622(a) as shown in the regulatory
text of this final rule.
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IX. Revisions to the Regulation Text To
Require IRFs To Submit Patient
Assessments on Medicare Advantage
Patients for Use in the ‘‘60 Percent
Rule’’ Calculations
A. Background on the ‘‘60 Percent Rule’’
Calculations
In order to be excluded from the acute
care inpatient hospital PPS specified in
§ 412.1(a)(1) and instead be paid under
the IRF PPS, rehabilitation hospitals and
units must meet, among other things,
the requirements in § 412.23(b)(2).
According to this section, at least 60
percent of an IRF’s total inpatient
population must require intensive
rehabilitative services for treatment of
one or more of 13 specified conditions.
The instructions that we provide to
Medicare contractors in Chapter 3,
section 140 of the Medicare Claims
Processing Manual, Internet-Only
Manual (IOM) Pub. 100–04, provide for
two methodologies that Medicare
contractors may use to determine
whether an IRF’s patient population
meets the requirements in
§ 412.23(b)(2). We refer to the first of
these two methodologies as the
‘‘presumptive methodology.’’ This
methodology uses the IRF–PAI
information that is submitted for
Medicare Part A fee-for-service
inpatients under § 412.604 and
§ 412.618. It is ‘‘presumptive’’ in that,
while § 412.23(b)(2) specifies that an
IRF’s total inpatient population must
meet the 60 percent rule requirements,
this method examines only the
Medicare patient data and extrapolates
from this the compliance percentage for
the IRF’s entire inpatient population.
The presumptive methodology uses
computer software to examine each
IRF–PAI for the presence of particular
diagnostic codes that indicate whether a
patient has one of the 13 medical
conditions listed in § 412.23(b)(2)(ii). If
the computer software determines that
the patient has one or more of the
diagnostic codes that represent one of
the 13 medical conditions listed in
§ 412.23(b)(2)(ii), then that patient is
counted in the presumptive
methodology calculation of that IRF’s
compliance percentage; otherwise, the
patient is not counted. Once the
computer software has examined all of
the IRF–PAIs submitted by a particular
IRF, the computer software computes
the presumptive compliance percentage
for that IRF. The percentage that the
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software computes is equal to the total
number of IRF–PAIs with one or more
diagnostic codes representing the 13
medical conditions listed in
§ 412.23(b)(2)(ii) divided by the total
number of IRF–PAIs submitted by the
IRF. This becomes the IRF’s
presumptive compliance percentage,
which is then compared with the
required minimum compliance
percentage to determine whether the
IRF has met the required minimum
compliance percentage for the
designated compliance review period.
In accordance with IOM instructions
in Chapter 3, section 140 of the
Medicare Claims Processing Manual, the
presumptive methodology described
above is used when the Medicare
contractor has verified that the IRF’s
Medicare Part A fee-for-service inpatient
population is representative of the
facility’s total inpatient population. For
this to be the case, the IOM instructions
specify that the IRF’s Medicare Part A
fee-for-service inpatient population
must be at least 50 percent or more of
the IRF’s total inpatient population. If
the IRF’s Medicare Part A fee-for-service
inpatient population is less than 50
percent of the IRF’s total inpatient
population, then we cannot verify that
the IRF–PAI data are representative of
the IRF’s total inpatient population.
Therefore, in these situations, we
require the Medicare contractors to use
the second of the 2 methodologies to
determine the IRF’s compliance
percentage.
The second methodology is
commonly known as the ‘‘medical
review’’ methodology. This
methodology requires the Medicare
contractor to review a sample of medical
records from the IRF’s total inpatient
population (which may consist of all of
the IRF’s medical records if the IRF has
100 or fewer inpatients during the
review period) to determine the IRF’s
compliance percentage. The medical
review methodology may be used at any
time at the discretion of the Medicare
contractor, but we specifically require
its use if the IRF’s Medicare Part A feefor-service inpatient population is less
than 50 percent of the IRF’s total
inpatient population (as described
above) or if the IRF fails to meet the
minimum compliance percentage using
the presumptive methodology.
B. Requirement To Submit Assessment
Data on Medicare Advantage Patients
As described above, the presumptive
methodology relies on the IRF–PAI data
that is submitted under § 412.604 and
§ 412.618. To use the presumptive
methodology, the Medicare Part A feefor-service inpatient population must
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make up at least 50 percent or more of
the IRF’s total inpatient population.
Since 2004, however, increasing
numbers of Medicare beneficiaries in
many areas of the country have been
enrolling in Medicare Advantage (MA)
plans rather than remaining in the
traditional Medicare Part A fee-forservice program. This, in turn, has led
to decreases in the number of Medicare
Part A fee-for-service inpatients in
certain IRFs across the country and has
resulted in a reduction in the number of
IRFs for whom the presumptive
methodology can be used.
Thus, although we have not required
IRFs to submit IRF–PAI data on MA
patients until now, we proposed in the
FY 2010 IRF PPS proposed rule (74 FR
21052, 21071 through 21073) to revise
the regulation text in § 412.604,
§ 412.606, § 412.610, § 412.614, and
§ 412.618 to require that IRFs submit
IRF–PAI data on all of their MA patients
to facilitate better calculations under the
60 percent rule. Where an IRF fails to
submit all MA IRF PAIs, we proposed
that CMS would not count the MA
patients in the compliance percentage
for that IRF. In addition, to ensure that
we receive all IRF–PAI data for all
Medicare patients, whether Part A or
Part C, we proposed to remove
§ 412.614(a)(3) of the regulations that
formerly allowed IRFs not to submit
IRF–PAI’s for Medicare patients for
whom they were not seeking payment
from Medicare. However, we
specifically solicited comments on
whether requiring IRFs to submit IRF–
PAI data on all of their MA patients
would be the best way to ensure the
integrity of the compliance review
process.
Requiring IRFs to submit IRF–PAIs for
all of their MA inpatients, in addition to
all of their Medicare Part A fee-forservice inpatients, will allow Medicare
contractors to begin using the
presumptive methodology to determine
IRFs’ compliance percentages when the
Part A fee-for-service and MA inpatient
populations combined are more than 50
percent of their total inpatient
populations. We proposed to preserve
the long-standing 5-year record
retention requirement for the IRF–PAIs
completed on Medicare Part A fee-forservice patients, as currently required in
§ 412.610(f), but we proposed a 10-year
record retention requirement for IRF–
PAIs completed on Medicare Part C
(Medicare Advantage) patients to
maintain consistency with the record
retention requirements for Medicare
Part C data specified in § 422.504(d).
We received 21 comments on the
proposed revisions to the regulation text
to require IRFs to submit patient
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assessments on MA patients for use in
the 60 percent rule calculations, which
are summarized below.
Comment: The majority of
commenters supported the proposed
change to the regulation text to allow
Medicare Advantage patients to be
counted in the 60 percent rule
calculations. However, individual
commenters offered differing
suggestions regarding the effective date
of the proposed change. One commenter
suggested that CMS delay implementing
the new reporting requirements until at
least FY 2011; another commenter
suggested rapid implementation of this
requirement so that the MA IRF–PAIs
could be used in the 60 percent
compliance calculations for current
compliance review periods that are
already underway as of October 1, 2009;
and a third commenter suggested that
the change should be made effective for
compliance review periods beginning
on or after October 1, 2009.
Response: We agree with the
commenters that it is important to
recognize the increasing population of
MA patients in many areas. We also
agree that this change will make the
compliance reviews easier for certain
IRFs with high percentages of MA
patients and for the fiscal intermediaries
or Medicare Administrative Contractors
that review these IRFs’ compliance with
the 60 percent rule. Further, we agree
with one of the commenter’s suggestions
that the change should be made
effective for compliance review periods
beginning on or after October 1, 2009
and we are adopting this effective date.
Comment: Several commenters
suggested that the proposed policy to
not use any of an IRF’s MA IRF–PAIs in
the compliance calculations if the IRF
does not submit all of them is overly
strict, and that we should allow for
some reasonable exceptions. Many of
these commenters also objected to the
proposed removal of the exception for
submission of IRF–PAIs on Part A feefor-service patients. However, one
commenter supported the proposed
requirements for submitting all of the
MA IRF–PAIs, indicating that it was a
‘‘fair and equitable’’ policy that would
avoid ‘‘cherry-picking’’ and reduce the
creation of unfair advantages among
IRFs.
Response: As we did not receive any
specific suggestions regarding a better
way of ensuring the integrity of the
compliance review process, we believe
that requiring IRFs to submit IRF–PAIs
on all of their MA patients and not
including MA patients in the
compliance calculations for those IRFs
that do not submit all of their MA IRF–
PAIs is the only way to ensure the
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integrity of the compliance review
process.
Comment: One commenter said that
IRFs might not always know the
Medicare identification numbers for
their MA patients, and suggested that
we provide a way for IRFs to send the
IRF–PAI data on MA patients without
the Medicare identification number.
Response: To preserve the integrity of
the compliance percentage review
process, we believe that it is important
to require that the patient’s Medicare
identification number be recorded on
the IRF–PAI for MA patients. Having the
Medicare identification numbers on the
IRF–PAIs will allow us to verify the
information that we obtain from the MA
IRF–PAIs with the MA claims that
hospitals are required to submit to CMS
for informational purposes. Currently,
all IPPS hospitals, IRFs, and long-term
care hospitals (LTCHs) are required to
submit abbreviated Medicare claims on
their MA patients for use in the DSH
and LIP adjustment calculations. To
enable IRFs to submit the required MA
claims, the Medicare managed care
organizations are already providing IRFs
with the Medicare beneficiary
identification numbers anytime an MA
patient is admitted to the IRF. Since
IRFs are already obtaining this
information for the MA claims, we do
not believe that it will be a problem for
IRFs to record this same information on
the IRF–PAIs.
Comment: One commenter suggested
that we change the wording in
§ 412.606(c)(1) to recognize that
multiple clinicians may provide
information for completing an IRF–PAI,
rather than specifying that only a single
clinician may complete it.
Response: We agree with the
commenter and are making the
suggested change.
Comment: One commenter suggested
that we revise the presumptive
methodology calculation to include
non-Medicare patients, including
patients that pay for their own IRF care.
Response: We will consider the
commenter’s suggestion. However, we
do not believe that we have the
authority to require IRFs to submit IRF–
PAIs on non-Medicare patients.
Comment: Several commenters
objected to the different record retention
requirements for the IRF–PAIs on Part A
fee-for-service patients and those on MA
patients.
Response: As noted previously, we
proposed to preserve the long-standing
5-year record retention requirement for
the IRF–PAIs completed on Medicare
Part A fee-for-service patients, as
currently required in § 412.610(f), but
we proposed a 10-year record retention
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39799
requirement for IRF–PAIs completed on
Medicare Part C (Medicare Advantage)
patients to maintain consistency with
the record retention requirements for
Medicare Part C data specified in
§ 422.504(d). We believe that the
proposed IRF–PAI record retention
requirements are the only way to
maintain consistency with the different
record retention requirements in each of
these two sections of the regulation.
Comment: Several commenters
suggested that we consider exceptions
to the proposed penalty for late
submission of the Medicare Advantage
IRF–PAIs and that the exceptions
should apply to both Medicare and
Medicare Advantage patients. One
commenter indicated that it would be
completely unreasonable for CMS to
impose the penalty of total exclusion of
the Medicare Advantage IRF–PAI data
based on one late submission.
Response: We understand the
concerns expressed by the commenters
and agree that a limited exception to
this policy is warranted. We currently
provide for a limited exception to the
application of the IRF–PAI penalty for
late submission under § 412.614(e). In
this final rule, we will amend section
412.614(e) to include late transmission
of MA IRF–PAIs, thereby providing for
a limited exception to the penalty for
late transmission of the MA IRF–PAIs
due to extraoridinary situations that are
beyond the control of the IRF.
Final Decision: After carefully
considering the comments that we
received on the proposed revisions to
the regulation text to require IRFs to
submit patient assessments on Medicare
Advantage patients for use in the 60
percent rule calculations, we are
finalizing the following revisions to the
regulation text in § 412.604, § 412.606,
§ 412.610, § 412.614, and § 412.618.
Specifically, we are adding Medicare
Part C (Medicare Advantage) patients to
the patients for whom IRFs must
complete and submit an IRF–PAI,
removing the paragraph that allows IRFs
not to submit IRF PAI data in instances
in which the IRF does not submit a
claim to Medicare, and rejecting MA
IRF–PAI data that is not complete. Thus,
we are finalizing the changes to the
regulation text as follows:
• In § 412.604(c), we are adding the
following sentence to the end of the
paragraph: ‘‘IRFs must also complete a
patient assessment instrument in
accordance with § 412.606 for each
Medicare Part C (Medicare Advantage)
patient admitted to or discharged from
an IRF on or after October 1, 2009.’’
Thus, the paragraph would read as
follows: ‘‘For each Medicare Part A feefor-service patient admitted to or
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discharged from an IRF on or after
January 1, 2002, the inpatient
rehabilitation facility must complete a
patient assessment instrument in
accordance with § 412.606. IRFs must
also complete a patient assessment
instrument in accordance with
§ 412.606 for each Medicare Part C
(Medicare Advantage) patient admitted
to or discharged from an IRF on or after
October 1, 2009.’’
• In § 412.606(b), we are adding the
phrase ‘‘and Medicare Part C (Medicare
Advantage)’’ after ‘‘fee-for-service’’ and
before ‘‘inpatients.’’ The paragraph
reads as follows: ‘‘An inpatient
rehabilitation facility must use the CMS
inpatient rehabilitation facility patient
assessment instrument to assess
Medicare Part A fee-for-service and
Medicare Part C (Medicare Advantage)
inpatients who—’’
• In § 412.606(c)(1), we are adding a
sentence at the end of the existing
paragraph that reads as follows: ‘‘IRFs
must also complete a patient assessment
instrument in accordance with
§ 412.606 for each Medicare Part C
(Medicare Advantage) patient admitted
to or discharged from an IRF on or after
October 1, 2009.’’
• In § 412.610(a), we are adding the
phrase ‘‘and Medicare Part C (Medicare
Advantage)’’ after ‘‘fee-for-service’’ and
before ‘‘inpatient.’’ The paragraph reads
as follows: ‘‘For each Medicare Part A
fee-for-service or Medicare Part C
(Medicare Advantage) inpatient, an
inpatient rehabilitation facility must
complete a patient assessment
instrument as specified in § 412.606 that
covers a time period that is in
accordance with the assessment
schedule specified in paragraph (c) of
this section.’’
• In § 412.610(b), we are adding the
phrase ‘‘or Medicare Part C (Medicare
Advantage)’’ after ‘‘fee-for-service’’ and
before ‘‘inpatient.’’ The paragraph reads
as follows: ‘‘The first day that the
Medicare Part A fee-for-service or
Medicare Part C (Medicare Advantage)
inpatient is furnished Medicare-covered
services during his or her current
inpatient rehabilitation facility hospital
stay is counted as day one of the patient
assessment schedule.’’
• In § 412.610(c), we are adding the
phrase ‘‘or Medicare Part C (Medicare
Advantage)’’ after ‘‘fee-for-service’’ and
before ‘‘patient’s.’’ The paragraph reads
as follows: ‘‘The inpatient rehabilitation
facility must complete a patient
assessment instrument upon the
Medicare Part A fee-for-service or
Medicare Part C (Medicare Advantage)
patient’s admission and discharge as
specified in paragraphs (c)(1) and (c)(2)
of this section.’’
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• In § 412.610(c)(1)(i)(A), we are
adding the phrase ‘‘or Medicare Part C
(Medicare Advantage)’’ after ‘‘fee-forservice’’ and before ‘‘hospitalization.’’
The paragraph reads as follows: ‘‘Time
period is a span of time that covers
calendar days 1 through 3 of the
patient’s current Medicare Part A feefor-service or Medicare Part C (Medicare
Advantage) hospitalization; * * *’’
• In § 412.610(c)(2)(ii)(B), we are
adding the phrase ‘‘or Medicare Part C
(Medicare Advantage)’’ after ‘‘fee-forservice’’ and before ‘‘inpatient,’’ so that
the resulting paragraph reads as follows:
‘‘The patient stops being furnished
Medicare Part A fee-for-service or
Medicare Part C (Medicare Advantage)
inpatient rehabilitation services.’’
• In § 412.610(f), we are adding the
phrase ‘‘and Medicare Part C (Medicare
Advantage) patients within the previous
10 years’’ after ‘‘5 years’’ and before
‘‘either,’’ and also adding the phrase
‘‘and produce upon request to CMS or
its contractors’’ after ‘‘obtain.’’ The
paragraph reads as follows: ‘‘An
inpatient rehabilitation facility must
maintain all patient assessment data sets
completed on Medicare Part A fee-forservice patients within the previous 5
years and Medicare Part C (Medicare
Advantage) patients within the previous
10 years either in a paper format in the
patient’s clinical record or in an
electronic computer file format that the
inpatient rehabilitation facility can
easily obtain and produce upon request
to CMS or its contractors.’’ This
maintains consistency with the 5-year
record retention requirements for IRF–
PAIs completed on Medicare Part A feefor-service patients specified in
§ 412.610(f) and the 10-year record
retention requirements for Medicare
Part C (Medicare Advantage) records
specified in § 422.504(d)(1)(ii).
• In § 412.614(a), we are adding the
phrase ‘‘and Medicare Part C (Medicare
Advantage)’’ after ‘‘fee-for-service’’ and
before ‘‘inpatient,’’ the paragraph reads
as follows: ‘‘The inpatient rehabilitation
facility must encode and transmit data
for each Medicare Part A fee-for-service
and Medicare Part C (Medicare
Advantage) inpatient—’’
• We are removing § 412.614(a)(3).
• In § 412.614(b)(1), we are adding
the phrase ‘‘and Medicare Part C
(Medicare Advantage)’’ after ‘‘fee-forservice’’ and before ‘‘inpatient,’’ the
paragraph reads as follows:
‘‘Electronically transmit complete,
accurate, and encoded data from the
patient assessment instrument for each
Medicare Part A fee-for-service and
Medicare Part C (Medicare Advantage)
inpatient to our patient data system in
accordance with the data format
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specified in paragraph (a) of this
section; and * * *’’
• We are revising § 412.614(d) to
read, ‘‘Consequences of failure to submit
complete and timely IRF–PAI data, as
required under paragraph (c) of this
section.’’
• We are revising § 412.614(d)(1) to
read, ‘‘Medicare Part A fee-for-service
data.’’
• We are making a technical
correction to the paragraph formerly
designated as § 412.614(d)(1) and
assigning the revised language to a new
paragraph § 412.614(d)(1)(a), which
reads as follows: ‘‘We assess a penalty
when an inpatient rehabilitation facility
does not transmit all of the required
data from the patient assessment
instrument for its Medicare Part A feefor-service patients to our patient data
system in accordance with the
transmission timeline in paragraph (c)
of this section.’’
• We are redesignating paragraph
§ 412.614(d)(2) as § 412.614(d)(1)(b).
• We are adding a new paragraph
§ 412.614(d)(2), which reads as follows:
‘‘Medicare Part C (Medicare Advantage)
data. Failure of the inpatient
rehabilitation facility to transmit all of
the required patient assessment
instrument data for its Medicare Part C
(Medicare Advantage) patients to our
patient data system in accordance with
the transmission timeline in paragraph
(c) of this section will result in a
forfeiture of the facility’s ability to have
any of its Medicare Part C (Medicare
Advantage) data used in the calculations
for determining the facility’s
compliance with the regulations at
§ 412.23(b)(2).’’
• We are revising the second sentence
in paragraph § 412.614(e). The sentence
reads as follows ‘‘Only CMS can
determine if a situation encountered by
an inpatient rehabilitation facility is
extraordinary and qualifies as a
situation for waiver of the penalty
specified in paragraph (d)(1)(ii) of this
section or for waiver of the forfeiture
specified in paragraph (d)(2) of this
section.’’
• In the introductory paragraph of
§ 412.618, we are adding the phrase ‘‘or
Medicare Part C (Medicare Advantage)’’
after ‘‘fee-for-service’’ and before
‘‘patient.’’ The paragraph reads as
follows: ‘‘For purposes of the patient
assessment process, if a Medicare Part A
fee-for-service or Medicare Part C
(Medicare Advantage) patient has an
interrupted stay, as defined under
§ 412.602, the following applies: * * *’’
X. Miscellaneous Comments
Comment: A commenter indicated
that posting extensive changes to the
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long-standing policies in the Medicare
Benefit Policy Manual on our Web site
for comment may violate the APA, and
they specifically cited Alaska
Professional Hunters Association, Inc. v.
Federal Aviation Administration, 177
F.3d 1030 (June 4, 1999).
Response: We disagree with the
commenter that the procedures used to
seek the public’s input on the new draft
manual provisions that will, when
finalized, be placed in Section 110 of
MBPM, and the proposal to rescind
HCFAR 85–2, violate the APA. We
proposed regulatory changes related to
IRF coverage policy through the FY
2010 IRF proposed rule. These
regulatory changes are being finalized
through this final rule with an
implementation date of January 1, 2010.
These regulatory provisions replace the
policies outlined in HCFAR 85–2. We
will therefore issue a notice in the
Federal Register at a future date to
rescind HCFAR 85–2, effective on the
date on which the replacement
regulations will take effect. While we
anticipate release of new manual
provisions that will interpret the new
regulations on that same date, the
substantive provisions in the
regulations, not the interpretive
guidance in the manuals, will replace
HCFAR 85–2. Full notice and comment
rulemaking was used to adopt these
regulations, in accordance with the
APA.
Thus, we believe that, in rescinding
the prior standard (HCFAR 85–2) in a
future notice to be issued in the Federal
Register and replacing it with new legal
standards in regulations, and
promulgating updated manual
provisions after consideration of public
comments to the proposed rule, we are
in compliance with all applicable and
necessary notice and comment
processes. Furthermore, by accepting
comments on the draft manual through
our Web site, and publicizing our
interest in receiving comments through
that mechanism in the proposed rule,
we exceeded the legal requirements for
seeking public comment on our draft
policies.
Comment: Several commenters
expressed concerns that the proposed
rule did not include a requirement for
rehabilitation nursing. They stated that
the importance of the rehabilitation
nursing staff to carry out medical
management interventions, repetition of
functional mobility techniques as taught
by the licensed therapists throughout
the patient’s stay, education in disease
management and illness prevention
related to a patient’s unique
presentation of diagnosis, family
training, and education cannot be
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underestimated in the IRF patient’s
potential for functional improvement.
One commenter suggested that CMS
revise the existing requirement to
require the use of certified registered
rehabilitation nurses.
Response: While we agree with the
commenters on the importance of
rehabilitation nursing, as well as the
need to ensure that patients are attended
to by licensed staff with experience in
rehabilitation nursing, we do not agree
that the requirements for rehabilitation
nursing should be included as an IRF
admission criterion. Instead, we believe
that the use of rehabilitation nurses is a
staffing requirement that would be
included in Conditions of Participation
for IRFs. We are actively working on
such Conditions and expect to release a
proposed rule in the near future.
Comment: One commenter requested
clarification on whether payments to an
IRF are reduced when patients are
transferred to a SNF. The commenter
stated that, occasionally, a patient will
be making steady progress toward goals
even up to four weeks after admission,
when family members suddenly change
their minds about their ability to care
for their loved one at home. The
commenter suggested that, if the IRF
keeps the patient beyond the average
length of stay for that CMG with the
intention of discharging the patient to a
home or community-based setting, the
IRF payment for the patient should not
be reduced.
Response: In the scenario that the
commenter described, the IRF payment
for the patient would not be reduced, as
long as the patient meets the IRF
coverage criteria. According to the
regulations, if the patient meets the IRF
coverage criteria and the patient’s length
of stay in the IRF is longer than the
average length of stay for the patient’s
CMG and tier, the IRF will receive the
full CMG payment for the patient
regardless of whether the patient is
discharged to a SNF.
Comment: One commenter suggested
that we clarify the composition of
prosthetic and orthotic services as well
as the specific qualifications of those
individuals that provide these services.
Response: An IRF is required to meet
the Hospital Conditions of Participation.
This means that, among other things, a
governing body is required to be
responsible for the services furnished in
an IRF, including prosthetic and
orthotic services, whether or not they
are furnished under contract. These
services must meet the general Medicare
requirements, which include
requirements for the professional
standards for those providing the
service.
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Comment: One commenter suggested
that CMS clarify the appeals process for
challenging removal of a facility from
the IRF PPS. The commenter proposed
removing IRFs only for the cost
reporting period following an
unfavorable decision by the Provider
Reimbursement Review Board (PRRB) or
the CMS Administrator.
Response: It is the responsibility of
the CMS Regional Office to notify the
IRF prior to the beginning of its next
cost reporting period if the facility has
failed to meet the IRF classification
requirements. This determination may
be appealed to the PRRB. However, an
IRF does not retain its IRF classification
status during the appeal process. The
process for appealing an IRF
declassification is described in 42 CFR
section 405, in Subpart R of the
regulations.
Comment: The Commission on
Accreditation of Rehabilitation
Facilities (CARF) indicated that, due to
the thoroughness of the CARF survey
procedure involving peer review and
the presumption that a facility with
such accreditation meets the majority of
the classification criteria (with the
ability to adjust the required criteria), it
would be appropriate for CMS to give
accreditation a more robust role in
determining IRF classification.
Therefore, they suggested that CMS
should give the CARF (and other
accrediting bodies as appropriate) the
responsibility for evaluating a facility’s
full compliance with the exclusion
criteria through its ongoing on-site
survey and peer review processes. In the
CARF’s view, any facility that is able to
obtain and maintain CARF accreditation
should be deemed to qualify as an IRF
for purposes of reimbursement under
the IRF PPS. Otherwise, the CARF
suggested that the current guidance in
the State Operations Manual, which
creates a presumption of satisfaction of
the exclusion criteria for accredited
facilities and programs, should be
maintained.
Response: The regulations at
§ 412.23(b) set forth the criteria used by
Medicare’s contractors to determine if a
hospital is excluded from the IPPS for
purposes of payment under the
Medicare program. One of these criteria,
commonly known as the ‘‘60 percent
rule,’’ focuses on the medical conditions
of patients admitted to an IRF. The
CARF accreditation criteria serve a
different function in that they define the
facility’s capacity to deliver services
rather than describing the patients being
served. As we have stated above, we are
actively working on Conditions of
Participation for IRFs and expect to
release a proposed rule in the near
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future. Thus, we believe that any role
that the CARF might assume in
determining IRF classifications in the
future would be related to deeming
authority under these ‘‘Conditions.’’
Comment: One commenter suggested
that we clarify whether the services of
aides may, in some instances, be used
to satisfy the ‘‘3 hour rule’’ in IRFs. The
commenter stated that, in other
Medicare programs such as therapy
reimbursed under Part B or through the
SNF PPS, aides cannot provide skilled
therapy, and the role of aides is limited
to the provision of support services.
Response: Therapy aides are
authorized to perform support services
for licensed and/or certified skilled
therapy practitioners. Services
performed by aides may be a useful
adjunct to the overall rehabilitation
program. However, therapy aide
services are not considered skilled, and
would not meet the IRF intensity of
therapy criterion used to evaluate the
appropriateness of IRF care.
Comment: One commenter suggested
that we clarify, with examples, when
Medicare coverage for an IRF stay is no
longer considered reasonable and
necessary.
Response: Under the IRF PPS, we
generally make one CMG payment to an
IRF for each Medicare discharge that is
considered reasonable and necessary
under section 1862(a)(1) of the Act. This
per discharge payment covers the
inpatient operating and capital costs of
furnishing covered rehabilitation
services to a Medicare patient
throughout the patient’s entire IRF stay.
Thus, defining the formal end of an IRF
stay is less important than it would be
if we were making payments by the day.
However, we believe that an IRF stay
should generally end when the patient
no longer requires or can reasonably be
expected to benefit significantly from
the services provided in an IRF. This
typically, though not in all cases, occurs
when the patient is ready to return
home or to a community-based
environment. We recognize that, in
certain limited instances, the patient
may need to be discharged to another
institutional setting of care, but we
believe that this would be a rare
occurrence.
Comment: One commenter suggested
that we clarify whether IRF claim
denials can be made exclusively by nonphysician reviewers, without a final
determination being made by a
physician reviewer.
Response: Medicare’s contractors
(including, but not limited to, fiscal
intermediaries, Medicare
Administrative Contractors (MACs), and
Recovery Audit Contractors (RACs)) are
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responsible for reviewing IRF claims to
ensure that they meet the reasonable
and necessary requirements for payment
of Medicare services under section
1862(a)(1) of the Act. Medicare’s
contractors typically use non-physician
reviewers, such as nurses or therapists,
to review Medicare claims, under the
supervision of physician medical
directors. Though we do not have a
formal process for the physician
medical directors to make the ‘‘final
determinations’’ on all IRF claims
denials, they are actively involved in
overseeing the reviews and ensuring the
integrity of the medical review process.
XI. Provisions in the Final Rule
In this final rule, we are adopting the
provisions as set forth in the FY 2010
IRF proposed rule (74 FR 21052), except
as noted elsewhere in the preamble.
Specifically:
A. Payment Provision Changes
• We will update the FY 2010 IRF
PPS relative weights and average length
of stay values using the most current
and complete Medicare claims and cost
report data in a budget neutral manner,
as discussed in section IV of this final
rule.
• We will update the FY 2010 IRF
facility level adjustments (rural, LIP,
and teaching status adjustments) using
the most current and complete Medicare
claims and cost report data in a budget
neutral manner, as discussed in section
V of this final rule.
• We will update the FY 2010 IRF
PPS payment rates by the proposed
market basket, as discussed in section
VI.A of this final rule.
• We will update the FY 2010 IRF
PPS payment rates by the wage index
and labor-related share in a budget
neutral manner, as discussed in sections
VI.A and B of this final rule.
• We will update the outlier
threshold amount for FY 2010, as
discussed in section VII.A of this final
rule.
• We will update the cost-to-charge
ratio ceiling and the national average
urban and rural cost-to-charge ratios for
purposes of determining the outlier
payments under the IRF PPS for FY
2010, as discussed in section VII.B of
this final rule.
B. Regulatory Text Changes
• We will remove the words ‘‘or
assessment’’ from § 412.23(b)(3) and
§ 412.29(b) to indicate that we are no
longer providing for a 3 to 10 day
inpatient assessment period after
admission to an IRF to assess the
appropriateness of the IRF admission, as
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discussed in section VIII.A of this final
rule.
• We will amend paragraphs
§ 412.23(b)(4) and § 412.29(c) to require
that IRFs ‘‘furnish, through the use of
qualified personnel, rehabilitation
nursing, physical therapy, and
occupational therapy, plus, as needed,
speech-language pathology, social
services, psychological services
(including neuropsychological services),
and orthotic and prosthetic services,’’ as
discussed in section VIII.I of this final
rule.
• We will replace the word
‘‘multidisciplinary’’ with the word
‘‘interdisciplinary’’ in § 412.23(b)(7) and
§ 412.29(e) to make the terminology
consistent with the new IRF coverage
criteria in § 412.622(a), as discussed in
section VIII.E of this final rule.
• We will require, in both
§ 412.23(b)(7) and § 412.29(e), that the
interdisciplinary team meetings occur at
least once per week (rather than once
every two weeks) to be consistent with
the new IRF coverage criteria in
§ 412.622(a), as discussed in section
VIII.E of this final rule.
• We will add new paragraphs (3),
(4), and (5) to § 412.622(a) to implement
new IRF coverage requirements, as
discussed in section VIII of this final
rule.
• With respect to § 412.604,
§ 412.606, § 412.610, § 412.614 and
§ 412.618, we will revise the regulation
text as described in section IX.B of this
final rule.
• With respect to § 412.614(a), we
will remove subparagraph (3) as
described in section IX.B of this final
rule.
• With respect to § 412.614(d), we are
making a technical correction to the
paragraph formerly designated as
paragraph (1) and assigning the revised
language to a new paragraph (1)(a),
redesignating paragraph (2) as (1)(b),
and adding a new paragraph (2), as
described in section IX.B of this final
rule.
XII. Collection of Information
Requirements
Under the Paperwork Reduction Act
of 1995, we are required to provide 30day notice in the Federal Register and
solicit public comment before a
collection of information requirement is
submitted to the Office of Management
and Budget (OMB) for review and
approval. In order to fairly evaluate
whether an information collection
should be approved by OMB, section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires that we
solicit comment on the following issues:
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• 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.
Therefore, we are soliciting public
comment on each of these issues for the
following sections of this document that
contain information collection
requirements:
Section 412.604 Conditions for
Payment Under the Prospective
Payment System for Inpatient
Rehabilitation Facilities
Section 412.604(c) states that for each
Medicare Part A fee-for-service patient
admitted to or discharged from an IRF
on or after January 1, 2002, the IRF must
complete a patient assessment
instrument in accordance with
§ 412.606. IRFs must also complete a
patient assessment instrument in
accordance with § 412.606 for each
Medicare Part C (Medicare Advantage)
patient admitted to or discharged from
an IRF on or after October 1, 2009.
The burden associated with this
requirement is the time and effort put
forth by each IRF to complete an average
of approximately 38 additional patient
assessment instruments each year
associated with its Medicare Part C
patients. We obtained the estimated
average number of Medicare Part C
patients in each IRF from the American
Medical Rehabilitation Providers
Association (AMRPA), based on
AMRPA’s own analysis of the
eRehabData® policy database. CMS
currently estimates that it takes the IRF
0.75 of an hour to complete a single
patient assessment instrument.
Therefore, the annual hour burden for
each IRF to complete approximately 38
additional patient assessment
instruments is 28.5 hours (38 × 0.75).
The total annual hour burden for all
1,205 IRFs is 34,342.5 hours (28.5 hours
× 1,205 IRFs). The burden estimate for
using the patient assessment instrument
for Medicare Part A is currently
approved under 0938–0842. CMS will
revise this currently approved package
as necessary to include any additional
burden placed on the IRF for submitting
the patient assessment instrument for
Medicare Advantage patients.
Section 412.606 Patient Assessments
Section 412.606 states that an IRF
must use the CMS inpatient
rehabilitation facility patient assessment
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instrument to assess Medicare Part A
fee-for-service and Medicare Part C
(Medicare Advantage) inpatients.
The burden for completing the patient
assessment instrument for Medicare Part
A is currently approved under 0938–
0842. CMS will revise this currently
approved package as necessary to
include any additional burden placed
on IRFs for submitting the patient
assessment instrument for Medicare
Advantage patients.
Section 412.610 Assessment Schedule
Section 412.610(f) states that an IRF
must maintain all patient assessment
data sets completed on Medicare Part A
fee-for-service patients within the
previous 5 years and Medicare Part C
(Medicare Advantage) patients within
the previous 10 years either in a paper
format in the patient’s clinical record or
in an electronic computer file format
that the inpatient rehabilitation facility
can easily obtain and produce upon
request to CMS or its contractors.
The burden for maintaining the
patient assessment instrument for
Medicare Part A is currently approved
under OMB# 0938–0842. CMS will
revise this currently approved package
as necessary to include any additional
burden placed on IRFs for maintaining
the patient assessment instrument for
Medicare Advantage patients.
Section 412.614 Transmission of
Patient Assessment Data
Section 412.614(a) requires that the
IRF must encode and transmit patient
assessment data to CMS.
The burden associated with this
requirement is the time staff must take
to transmit the data. CMS currently
estimates that it takes the IRF 0.10 of an
hour to transmit a single patient
assessment instrument. Therefore, the
annual hour burden to transmit an
average of approximately 38 additional
patient assessment instruments per IRF
is 3.8 hours (38 × 0.10). The total annual
hour burden for all 1,205 IRFs is 4,579
hours (3.8 hours × 1,205 IRFs). The
burden estimate for transmitting the
patient assessment instrument for
Medicare Part A is currently approved
under 0938–0842. CMS will revise this
currently approved package as
necessary to include any additional
burden placed on the IRF for
transmitting the patient assessment
instrument for Medicare Advantage
patients.
Section 412.622 IRF Coverage Criteria
Section 412.622(a)(4)(i) requires that a
comprehensive screening meet all of the
requirements in paragraphs (A) through
(E). Section 412(a)(4)(i)(D) requires the
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physician to document his or her
concurrence with the findings and
results of the preadmission screening.
Section 412(a)(4)(i)(E) requires that the
preadmission screening be retained in
the patient’s medical record.
The burden associated with these
requirements is the time and effort put
forth by the rehabilitation physician to
document his or her concurrence with
the preadmission findings and the
results of the preadmission screening
and retain the information in the
patient’s medical record. The burden
associated with these requirements is in
keeping with the ‘‘Condition of
Participation: Medical record services,’’
that are already applicable to Medicare
participating hospitals. The burden
associated with these requirements is
currently approved under OMB# 0938–
0328. As stated in the approved
Hospital CoPs Supporting Statement, we
believe that these requirements reflect
customary and usual business and
medical practice. Thus, in accordance
with section 1320.3(b)(2) of the Act, the
burden is not subject to the PRA.
Section 412.622(a)(4)(ii) is consistent
with the existing Hospital CoP
requirement at § 482.24(c)(2) which
requires the facility to have and utilize
a post-admission evaluation process.
The post-admission evaluation process
requires that a rehabilitation physician
complete a post-admission evaluation
for each patient within 24 hours of that
patient’s admission to the IRF, compare
it to that noted in the preadmission
screening documentation, and begin
development of the overall
individualized plan of care. Similarly,
§ 482.24(c)(2) requires that the postadmission physician evaluation be
retained in the patient’s medical record
in keeping with the Hospital CoPs.
The burden associated with these
requirements is the time and effort put
forth by the rehabilitation physician to
document the patient’s status on
admission to the IRF, compare it to that
noted in the preadmission screening
document, begin development of the
care plan, and retain the information in
the patient’s medical record. The
burden associated with these
requirements is consistent with the
‘‘Condition of Participation: Medical
record services,’’ that is already
applicable to Medicare participating
hospitals. The burden associated with
this requirement is currently approved
under OMB# 0938–0328. As stated in
the approved Hospital CoPs Supporting
Statement, we believe that these
requirements reflect customary and
usual business and medical practice.
Thus, in accordance with section
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1320.3(b)(2) of the Act, the burden is not
subject to the PRA.
The requirements in section 412.622
(a)(4)(iii) regarding an individualized
plan of care are consistent with the
existing Hospital CoPs at § 482.56(b) to
develop an overall plan of care for each
IRF admission. Similarly, the
individualized plan of care required by
412.622(a)(4)(iii)(A) would be required
to be retained in the patient’s medical
record, as currently required by the
Hospital CoPs at § 482.24(c)(2).
The burden associated with these
requirements is the time and effort put
forth by the rehabilitation physician to
develop the individualized overall plan
of care and retain the individualized
overall plan of care in the patient’s
medical record. The burden associated
with these requirements is in keeping
with the ‘‘Condition of Participation:
Medical record services,’’ and
‘‘Condition of Participation:
Rehabilitation services. Standard:
Delivery of Services’’ that are already
applicable to Medicare participating
hospitals. The burden associated with
these requirements is currently
approved under OMB# 0938–0328. As
stated in the approved Hospital CoPs
Supporting Statement, we believe that
these requirements reflect customary
and usual business and medical
practice. Thus, in accordance with
section 1320.3(b)(2) of the Act, the
burden is not subject to the PRA.
Section 412.622(a)(5) requires the
interdisciplinary team to meet at least
once per week throughout the duration
of the patient’s stay to implement
appropriate treatment services; review
the patient’s progress toward stated
rehabilitation goals; identify any
problems that could impede progress
towards those goals; and, where
necessary, reassess previously
established goals in light of
impediments, revise the treatment plan
in light of new goals, and monitor
continued progress toward those goals.
It also requires that the rehabilitation
physician document his or her
concurrence with the results and
findings of the team meeting and that
documentation of the weekly meetings
be retained in the patient’s medical
record.
The burden associated with these
requirements is the time spent
documenting the weekly meetings and
the concurrence of the rehabilitation
physician with the results and findings
of the team meeting and retaining the
information in the patient’s medical
record. The burden associated with
these proposed requirements is
consistent with the ‘‘Condition of
Participation: Medical record services,’’
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that are already applicable to Medicare
participating hospitals. The burden
associated with these requirements is
currently approved under OMB# 0938–
0328. As stated in the approved
‘‘Hospital CoPs Supporting Statement,’’
we believe that the proposed
requirements reflect customary and
usual business and medical practice.
Thus, in accordance with section
1320.3(b)(2) of the Act, the burden is not
subject to the PRA.
You may submit comments on these
information collection and
recordkeeping requirements in one of
the following ways (please choose only
one of the ways listed):
1. Submit your comments
electronically as specified in the
ADDRESSES section of this proposed rule;
or
2. Submit your written comments to
the Office of Information and Regulatory
Affairs, Office of Management and
Budget, Attention: CMS Desk Officer,
[CMS–1538–F], Fax: (202) 395–7245; or
E-mail: OIRA_submission@omb.eop.gov.
XIII. Regulatory Impact Analysis
A. Overall Impact
We have examined the impacts of this
final rule as required by Executive
Order 12866 (September 30, 1993,
Regulatory Planning and Review), the
Regulatory Flexibility Act (RFA,
September 19, 1980, Pub. L. 96–354),
section 1102(b) of the Social Security
Act, section 202 of the Unfunded
Mandates Reform Act of 1995 (Pub. L.
104–4), Executive Order 13132 on
Federalism (August 4, 1999), and the
Congressional Review Act (5 U.S.C.
804(2)).
Executive Order 12866 directs
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). A regulatory impact
analysis (RIA) must be prepared for
major rules with economically
significant effects ($100 million or more
in any one year). This final rule is a
major rule, as defined in Title 5, United
States Code, section 804(2), because we
estimate the impact to the Medicare
program, and the annual effects to the
overall economy, will be more than
$100 million. We estimate that the total
impact of these changes for estimated
FY 2010 payments compared to
estimated FY 2009 payments will be an
increase of approximately $145 million
due to the update to the payment rates.
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The Regulatory Flexibility Act (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 IRFs and most other
providers and suppliers are small
entities, either by nonprofit status or by
having revenues of $7 million to $34.5
million in any one year. (For details, see
the Small Business Administration’s
final rule that set forth size standards for
health care industries, at 65 FR 69432 at
https://www.sba.gov/idc/groups/public/
documents/sba_homepage/
serv_sstd_tablepdf.pdf, November 17,
2000.) Because we lack data on
individual hospital receipts, we cannot
determine the number of small
proprietary IRFs or the proportion of
IRFs’ revenue that is derived from
Medicare payments. Therefore, we
assume that all IRFs (an approximate
total of 1,200 IRFs, of which
approximately 60 percent are nonprofit
facilities) are considered small entities
and that Medicare payment constitutes
the majority of their revenues. The
Department of Health and Human
Services generally uses a revenue
impact of 3 to 5 percent as a significance
threshold under the RFA. As shown in
Table 7, we estimate that the net
revenue impact of this final rule on all
IRFs is to increase estimated payments
by about 2.5 percent, with an estimated
positive increase in payments of 3
percent or higher for some categories of
IRFs (such as urban IRFs in the East
South Central, West North Central, West
South Central, Mountain and Pacific
regions) and an estimated decrease in
payments of 3.8 percent for the 17 IRFs
that have a resident to ADC ratio greater
than 19 percent. Thus, we anticipate
that this final rule would have a
significant impact on a substantial
number of small entities. Medicare
fiscal intermediaries and carriers are not
considered to be small entities.
Individuals and States are not included
in the definition of a small entity.
In addition, section 1102(b) of the Act
requires us to prepare a regulatory
impact analysis if a rule may have a
significant impact on the operations of
a substantial number of small rural
hospitals. This analysis must conform to
the provisions of section 604 of the
RFA. For purposes of section 1102(b) of
the Act, we define a small rural hospital
as a hospital that is located outside of
a Metropolitan Statistical Area and has
fewer than 100 beds. As discussed in
detail below, the rates and policies set
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forth in this final rule will not have an
adverse impact on rural hospitals based
on the data of the 184 rural units and
21 rural hospitals in our database of
1,181 IRFs for which data were
available.
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 one year of
$100 million in 1995 dollars, updated
annually for inflation. In 2009, that
threshold level is approximately $133
million. This final rule will not impose
spending costs on State, local, or tribal
governments, in the aggregate, or by the
private sector, of $133 million.
Executive Order 13132 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.
As stated above, this final rule will not
have a substantial effect on State and
local governments, preempt State law,
or otherwise have a Federalism
implication.
B. Anticipated Effects of the Final Rule
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1. Basis and Methodology of Estimates
This final rule sets forth updates of
the IRF PPS rates contained in the FY
2009 final rule and updates to the CMG
relative weights and length of stay
values, the facility-level adjustments,
the wage index, and the outlier
threshold for high-cost cases.
We estimate that the FY 2010 impact
will be a net increase of $145 million in
payments to IRF providers. The impact
analysis in Table 7 of this final rule
represents the projected effects of the
final policy changes in the IRF PPS for
FY 2010 compared with estimated IRF
PPS payments in FY 2009 without the
policy changes. We determine the
effects by estimating payments while
holding all other payment variables
constant. We use the best data available,
but we do not attempt to predict
behavioral responses to these changes,
and we do not make adjustments for
future changes in such variables as
number of discharges or case-mix.
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 forecasting errors because
of other changes in the forecasted
impact time period. Some examples
could be legislative changes made by
the Congress to the Medicare program
that would impact program funding, or
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changes specifically related to IRFs.
Although some of these changes may
not necessarily be specific to the IRF
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 IRFs.
In updating the rates for FY 2010, we
are implementing a number of standard
annual revisions and clarifications
mentioned elsewhere in this final rule
(for example, the update to the wage
and market basket indexes used to
adjust the Federal rates). We estimate
that these revisions would increase
payments to IRFs by approximately
$145 million (all due to the update to
the market basket index, since the
update to the wage index is done in a
budget neutral manner—as required by
statute—and therefore neither increases
nor decreases aggregate payments to
IRFs).
The effects of the changes that impact
IRF PPS payment rates are shown in
Table 7. The following changes that
affect the IRF PPS payment rates are
discussed separately below:
• The effects of the update to the
outlier threshold amount, consistent
with section 1886(j)(4) of the Act.
• The effects of the annual market
basket update (using the RPL market
basket) to IRF PPS payment rates, as
required by section 1886(j)(3)(A)(i) and
section 1886(j)(3)(C) of the Act.
• The effects of applying the budgetneutral labor-related share and wage
index adjustment, as required under
section 1886(j)(6) of the Act.
• The effects of the budget-neutral
changes to the CMG relative weights
and length of stay values, under the
authority of section 1886(j)(2)(C)(i) of
the Act.
• The effects of the budget-neutral
changes to the facility-level adjustment
factors, as permitted under section
1886(j)(3)(A)(v) of the Act.
• The total change in estimated
payments based on the FY 2010 policy
changes relative to estimated FY 2009
payments without the policy changes.
2. Description of Table 7
The table below categorizes IRFs by
geographic location, including urban or
rural location, and location with respect
to CMS’s nine census divisions (as
defined on the cost report) of the
country. In addition, the table divides
IRFs into those that are separate
rehabilitation hospitals (otherwise
called freestanding hospitals in this
section), those that are rehabilitation
units of a hospital (otherwise called
hospital units in this section), rural or
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urban facilities, ownership (otherwise
called for-profit, non-profit, and
government), and by teaching status.
The top row of the table shows the
overall impact on the 1,181 IRFs
included in the analysis.
The next 12 rows of Table 7 contain
IRFs categorized according to their
geographic location, designation as
either a freestanding hospital or a unit
of a hospital, and by type of ownership;
all urban, which is further divided into
urban units of a hospital, urban
freestanding hospitals, and by type of
ownership; and all rural, which is
further divided into rural units of a
hospital, rural freestanding hospitals,
and by type of ownership. There are 976
IRFs located in urban areas included in
our analysis. Among these, there are 776
IRF units of hospitals located in urban
areas and 200 freestanding IRF hospitals
located in urban areas. There are 205
IRFs located in rural areas included in
our analysis. Among these, there are 184
IRF units of hospitals located in rural
areas and 21 freestanding IRF hospitals
located in rural areas. There are 390 forprofit IRFs. Among these, there are 321
IRFs in urban areas and 69 IRFs in rural
areas. There are 724 non-profit IRFs.
Among these, there are 603 urban IRFs
and 121 rural IRFs. There are 67
government-owned IRFs. Among these,
there are 52 urban IRFs and 15 rural
IRFs.
The remaining three parts of Table 7
show IRFs grouped by their geographic
location within a region and by teaching
status. First, IRFs located in urban areas
are categorized with respect to their
location within a particular one of the
nine CMS geographic regions. Second,
IRFs located in rural areas are
categorized with respect to their
location within a particular one of the
nine CMS geographic regions. In some
cases, especially for rural IRFs located
in the New England, Mountain, and
Pacific regions, the number of IRFs
represented is small. Finally, IRFs are
grouped by teaching status, including
non-teaching IRFs, IRFs with an intern
and resident to average daily census
(ADC) ratio less than 10 percent, IRFs
with an intern and resident to ADC ratio
greater than or equal to 10 percent and
less than or equal to 19 percent, and
IRFs with an intern and resident to ADC
ratio greater than 19 percent.
The estimated impacts of each change
to the facility categories listed above are
shown in the columns of Table 7. The
description of each column is as
follows:
Column (1) shows the facility
classification categories described
above.
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Column (2) shows the number of IRFs
in each category in our FY 2008 analysis
file.
Column (3) shows the number of
cases in each category in our FY 2008
analysis file.
Column (4) shows the estimated effect
of the adjustment to the outlier
threshold amount.
Column (5) shows the estimated effect
of the market basket update to the IRF
PPS payment rates.
Column (6) shows the estimated effect
of the update to the IRF labor-related
share and wage index, in a budget
neutral manner.
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Column (7) shows the estimated effect
of the update to the CMG relative
weights and average length of stay
values, in a budget neutral manner.
Column (8) shows the estimated effect
of the update to the facility-level
adjustment factors (rural, LIP, and
teaching status), in a budget neutral
manner.
Column (9) compares our estimates of
the payments per discharge,
incorporating all of the changes
reflected in this final rule for FY 2010,
to our estimates of payments per
discharge in FY 2009(without these
changes).
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The average estimated increase for all
IRFs is approximately 2.5 percent,
which is entirely due to the market
basket update. Since the update to the
outlier threshold amount does not
impact aggregate payments this year,
and since we are making the remainder
of the changes outlined in this final rule
in a budget-neutral manner, the other
changes being made in this final rule
will not affect total estimated IRF
payments in the aggregate. However, as
described in more detail in each section,
they will affect the estimated
distribution of payments among
providers.
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3. Impact of the Update to the Outlier
Threshold Amount
The outlier threshold adjustment is
presented in column 4 of Table 7. We
estimate that IRF outlier payments as a
percentage of total estimated IRF
payments are 3 percent in FY 2009.
Therefore, since we estimate that we
have achieved the target percentage in
FY 2009, we are adjusting the outlier
threshold amount in this final rule
solely to account for the 2.5 percent
market basket adjustment for FY 2010
(as discussed in section VI.A of this
final rule) and the FY 2010 updates to
the facility-level adjustments (as
discussed in section V of this final rule)
so that we will continue to maintain
estimated outlier payments at 3 percent
of total estimated aggregate IRF
payments for FY 2010.
Since we estimate that we achieved
the 3 percent target in FY 2009, and that
estimated outlier payments will
continue to equal 3 percent of total
estimated payments in FY 2010, there is
no overall impact on FY 2010 aggregate
payments from this update. However,
we estimate slight impacts on
individual groups of IRFs, which are so
small that they round to 0.0 percent.
However, Medicare pays an unusually
high percentage of outlier payments (8.3
percent) to rural IRFs in the Pacific
region. Thus, the estimated impact of
the update to the outlier threshold
amount for FY 2010 just rounds to 0.1
percent for these 5 IRFs.
4. Impact of the Market Basket Update
to the IRF PPS Payment Rates
The market basket update to the IRF
PPS payment rates is presented in
column 5 of Table 7. In the aggregate the
update would result in a 2.5 percent
increase in overall estimated payments
to IRFs.
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5. Impact of the CBSA Wage Index and
Labor-Related Share
In column 6 of Table 7, we present the
effects of the budget neutral update of
the wage index and labor-related share.
The changes to the wage index and the
labor-related share are discussed
together because the wage index is
applied to the labor-related share
portion of payments, so the changes in
the two have a combined effect on
payments to providers. As discussed in
section VI.A of this final rule, the laborrelated share increased from 75.464
percent in FY 2009 to 75.779 percent in
FY 2010.
In the aggregate and for all urban
IRFs, we do not estimate that these
changes will affect overall estimated
payments to IRFs. However, we estimate
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that these changes will have small
distributional effects. We estimate a 0.1
percent increase in payments to rural
IRFs, with the largest increase in
payments of 1.4 percent for urban IRFs
in the Pacific region. We estimate the
largest decrease in payments from the
update to the CBSA wage index and
labor-related share to be a 0.8 percent
decrease for IRFs with an intern and
resident to ADC ratio greater than or
equal to 10 percent and less than or
equal to 19 percent.
6. Impact of the Update to the CMG
Relative Weights and Average Length of
Stay Values
In column 7 of Table 7, we present the
effects of the budget neutral update of
the CMG relative weights and average
length of stay values. In the aggregate
we do not estimate that these changes
will affect overall estimated payments to
IRFs. However, these changes have
small distributional effects, with the
largest effect being a decrease in
payments of 0.3 percent to IRFs in the
Rural Pacific region.
7. Impact of the Update to the Rural,
LIP, and Teaching Status Adjustment
Factors
In column 8 of Table 7, we present the
effects of the budget neutral update to
the rural, LIP, and teaching status
adjustment factors. In the aggregate, we
do not estimate that these changes will
affect overall estimated payments to
IRFs. However, we estimate that these
changes will have small distributional
effects. We estimate the largest increase
in payments to be a 0.7 percent increase
for urban IRFs in the East South Central
region. We estimate the largest decrease
in payments to be a 6.3 percent decrease
for teaching IRFs with a resident to ADC
ratio greater than 19 percent. The
estimated decrease in payments for
teaching IRFs, of between 0.9 percent
and 6.3 percent depending on the IRF’s
intern and resident to average daily
census ratio, is caused by the decrease
in the teaching status adjustment factor
from 0.9012 to 0.6876, as discussed in
section V of this final rule. We also
estimate decreases in payments to rural
IRFs due to the decrease in the rural
adjustment from 21.3 percent in FY
2009 to 18.4 percent in FY 2010, and
slight distributional effects among
facilities due to the decrease in the LIP
adjustment factor from 0.6229 in FY
2009 to 0.4613 in FY 2010. Both the
rural and the LIP adjustment factors are
discussed in section V.A of this final
rule.
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C. Alternatives Considered
Because we have determined that this
final rule would have a significant
economic impact on IRFs and on a
substantial number of small entities, we
will discuss the alternative changes to
the IRF PPS that we considered.
Section 1886(j)(3)(C) of the Act
requires the Secretary to update the IRF
PPS payment rates by an increase factor
that reflects changes over time in the
prices of an appropriate mix of goods
and services included in the covered
IRF services. As noted in section V of
this final rule, in the absence of
statutory direction on the FY 2010
market basket increase factor, it is our
understanding that the Congress
requires a full market basket increase
factor based upon current data. Thus,
we did not consider alternatives to
updating payments using the estimated
RPL market basket increase factor
(currently 2.5 percent) for FY 2010.
We considered maintaining the
existing CMG relative weights and
average length of stay values for FY
2010. However, several commenters on
the FY 2009 IRF PPS proposed rule (73
FR 46373) suggested that the data that
we used for FY 2009 to update the CMG
relative weights and average length of
stay values did not fully reflect recent
changes in IRF utilization that have
occurred because of changes in the IRF
compliance percentage and the
consequences of recent IRF medical
necessity reviews. In light of recently
available data and our desire to ensure
that the CMG relative weights and
average length of stay values are as
reflective as possible of these recent
changes and that IRF PPS payments
continue to reflect as accurately as
possible the current costs of care in
IRFs, we believe that it is appropriate to
update the CMG relative weights and
average length of stay values at this
time.
We also considered maintaining the
existing rural, LIP, and teaching status
adjustment factors for FY 2010.
However, the current rural, LIP, and
teaching status adjustment factors are
based on RAND’s analysis of FY 2003
data, which are not reflective of recent
changes in IRF utilization that have
occurred because of changes in the IRF
compliance percentage and the
consequences of recent IRF medical
necessity reviews. Thus, we believe that
it is important to update these
adjustment factors at this time to ensure
that payments to IRFs reflect as
accurately as possible the current costs
of care in IRFs.
In estimating the updates to the rural,
LIP, and teaching status adjustment
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factors, we considered either basing
them on an analysis of FY 2008 data
alone, or averaging the adjustment
factors based on the most recent three
years of data (FYs 2006, 2007, and
2008). We decided to propose the new
approach of averaging the adjustment
factors based on the most recent three
years of data to avoid unnecessarily
large fluctuations in the adjustment
factors from year to year, and thereby
promote the consistency and
predictability of IRF PPS payments over
time. We believe that this will benefit
all IRFs by enabling them to plan their
future Medicare payments more
accurately.
We considered maintaining the
existing outlier threshold amount for FY
2010. However, we needed to update
the outlier threshold amount to account
for the 2.5 percent market basket
increase to IRF PPS payments and the
effects of the changes to the facilitylevel adjustment factors to maintain
estimated outlier payments at 3 percent
of estimated total payments for FY 2010.
Thus, we believe that this update is
appropriate for FY 2010.
In addition, we considered
maintaining the existing coverage
requirements for IRFs, without
clarification. However, these coverage
requirements have not been updated in
over 20 years and no longer reflect
current medical practice or changes that
have occurred in IRF utilization and
payments as a result of the
implementation of the IRF PPS in 2002.
We believe that the clarifications would
benefit IRFs and Medicare’s contractors
(including fiscal intermediaries,
Medicare Administrative Contractors,
and Recovery Audit Contractors) by
promoting a more consistent
understanding of CMS’s IRF coverage
policies among stakeholders, thereby
leading to fewer disputed IRF claims
denials.
Finally, we considered maintaining
our current policy of requiring that an
IRF’s Medicare Part A inpatient
population consist of at least 50 percent
or more of the facility’s total inpatient
population before the presumptive
methodology can be used to calculate
the IRF’s compliance percentage under
the 60 percent rule. However, increasing
numbers of Medicare beneficiaries in
many areas of the country have been
enrolling in Medicare Advantage (MA)
plans rather than remaining in the
traditional Medicare Part A fee-forservice program. This, in turn, has led
to decreases in the number of Medicare
Part A fee-for-service inpatients in
certain IRFs across the country and has
resulted in a reduction in the number of
IRFs that can benefit from the
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presumptive methodology. We did not
anticipate this result when the policy
was implemented. In light of these
recent trends, we believe that it is
appropriate at this time to include the
Medicare Advantage patients in the
calculations for the purposes of using
the presumptive methodology to
determine IRFs’ compliance with the 60
percent rule requirements.
D. Accounting Statement
As required by OMB Circular A–4
(available at https://
www.whitehouse.gov/omb/circulars/
a004/a-4.pdf), in Table 8 below, we
have prepared an accounting statement
showing the classification of the
expenditures associated with the
provisions of this final rule. This table
provides our best estimate of the
increase in Medicare payments under
the IRF PPS as a result of the changes
presented in this final rule based on the
data for 1,181 IRFs in our database. All
estimated expenditures are classified as
transfers to Medicare providers (that is,
IRFs).
TABLE 8—ACCOUNTING STATEMENT:
CLASSIFICATION OF ESTIMATED EXPENDITURES, FROM THE 2009 IRF
PPS FISCAL YEAR TO THE 2010 IRF
PPS FISCAL YEAR
Category
Annualized Monetized
Transfers.
From Whom to
Whom?
Transfers
$145 million.
Federal Government
to IRF Medicare
Providers.
E. Conclusion
Overall, the estimated payments per
discharge for IRFs in FY 2010 are
projected to increase by 2.5 percent,
compared with those in FY 2009, as
reflected in column 9 of Table 7. IRF
payments are estimated to increase 2.7
percent in urban areas and 1.1 percent
in rural areas, per discharge compared
with FY 2009. Payments to
rehabilitation units in urban areas are
estimated to increase 2.5 percent per
discharge. Payments to rehabilitation
freestanding hospitals in urban areas are
estimated to increase 2.9 percent per
discharge. Payments to rehabilitation
units in rural areas are estimated to
increase 1.2 percent per discharge,
while payments to freestanding
rehabilitation hospitals in rural areas are
estimated to increase 1.0 percent per
discharge.
Overall, the largest payment increase
is estimated at 3.6 percent for urban
IRFs in the Mountain region. Teaching
IRFs with a resident to ADC ratio greater
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39809
than 19 percent are estimated to have
the largest decrease of 3.8 percent in
payments.
We received 1 comment on the
regulatory impact analysis, which is
summarized below.
Comment: One commenter indicated
that the information provided in the
regulatory impact analysis for the
proposed rule was not sufficient to
allow the public to calculate the impacts
for individual IRFs. This commenter
suggested that we add additional
columns, including information about
the FY 2009 estimated average weight
per discharge, the FY 2009 estimated
outlier payments, and the FY 2009 total
estimated payments to the IRF rate
setting file that we post on the IRF PPS
Web site in conjunction with each
proposed and final rule.
Response: To provide as much
information as possible to enable the
public to analyze the impacts of our
policies, we will add the suggested
information to the IRF rate setting file
that we will post on the IRF PPS Web
site at https://www.cms.hhs.gov/
InpatientRehabFacPPS/
07_DataFiles.asp#TopOfPage in
conjunction with this final rule.
In accordance with the provisions of
Executive Order 12866, this regulation
was reviewed by the Office of
Management and Budget.
List of Subjects in 42 CFR Part 412
Administrative practice and
procedure, Health facilities, Medicare,
Puerto Rico, Reporting and
recordkeeping requirements.
■ For the reasons set forth in the
preamble, the Centers for Medicare &
Medicaid Services amends 42 CFR
chapter IV as follows:
PART 412—PROSPECTIVE PAYMENT
SYSTEMS FOR INPATIENT HOSPITAL
SERVICES
1. The authority citation for part 412
is amended to read as follows:
■
Authority: Sections 1102, 1862, and 1871
of the Social Security Act (42 U.S.C. 1302,
1395y, and 1395hh).
Subpart B—Hospital Services Subject
to and Excluded From the Prospective
Payment Systems for Inpatient
Operating Costs and Inpatient CapitalRelated Costs
■
■
■
■
2. Section 412.23 is amended by—
A. Revising paragraph (b)(3).
B. Revising paragraph (b)(4).
C. Revising paragraph (b)(7).
The revisions read as follows:
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§ 412.23 Excluded hospitals:
Classifications.
*
*
*
*
*
(b) * * *
(3) Have in effect a preadmission
screening procedure under which each
prospective patient’s condition and
medical history are reviewed to
determine whether the patient is likely
to benefit significantly from an intensive
inpatient hospital program.
(4) Ensure that the patients receive
close medical supervision and furnish,
through the use of qualified personnel,
rehabilitation nursing, physical therapy,
and occupational therapy, plus, as
needed, speech-language pathology,
social services, psychological services
(including neuropsychological services),
and orthotic and prosthetic services.
*
*
*
*
*
(7) Use a coordinated
interdisciplinary team approach in the
rehabilitation of each inpatient, as
documented by the periodic clinical
entries made in the patient’s medical
record to note the patient’s status in
relationship to goal attainment, and that
team conferences are held at least once
per week to determine the
appropriateness of treatment.
*
■
■
■
■
*
*
*
*
3. Section 412.29 is amended by—
A. Revising paragraph (b).
B. Revising paragraph (c).
C. Revising paragraph (e).
The revisions read as follows:
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4. Section 412.604 is amended by
revising paragraph (c) to read as follows:
■
§ 412.604 Conditions for payment under
the prospective payment system for
inpatient rehabilitation facilities.
*
*
*
*
*
(c) Completion of patient assessment
instrument. For each Medicare Part A
fee-for-service patient admitted to or
discharged from an IRF on or after
January 1, 2002, the inpatient
rehabilitation facility must complete a
patient assessment instrument in
accordance with § 412.606. IRFs must
also complete a patient assessment
instrument in accordance with
§ 412.606 for each Medicare Part C
(Medicare Advantage) patient admitted
to or discharged from an IRF on or after
October 1, 2009.
*
*
*
*
*
5. Section 412.606 is amended by—
A. Revising paragraph (b) introductory
text.
■ B. Revising paragraph (c)(1).
The revisions read as follows:
■
■
Patient assessments.
*
*
*
*
*
(b) Have in effect a preadmission
screening procedure under which each
prospective patient’s condition and
medical history are reviewed to
determine whether the patient is likely
to benefit significantly from an intensive
inpatient hospital program.
(c) Ensure that the patients receive
close medical supervision and furnish,
through the use of qualified personnel,
rehabilitation nursing, physical therapy,
and occupational therapy, plus, as
needed, speech-language pathology,
social services, psychological services
(including neuropsychological services),
and orthotic and prosthetic services.
*
*
*
*
*
(e) Use a coordinated
interdisciplinary team approach in the
rehabilitation of each inpatient, as
documented by the periodic clinical
entries made in the patient’s medical
record to note the patient’s status in
relationship to goal attainment, and that
team conferences are held at least once
*
*
*
*
(b) Patient assessment instrument. An
inpatient rehabilitation facility must use
the CMS inpatient rehabilitation facility
patient assessment instrument to assess
Medicare Part A fee-for-service and
Medicare Part C (Medicare Advantage)
inpatients who—
*
*
*
*
*
(c) * * *
(1) A clinician of the inpatient
rehabilitation facility must perform a
comprehensive, accurate, standardized,
and reproducible assessment of each
Medicare Part A fee-for-service inpatient
using the inpatient rehabilitation facility
patient assessment instrument specified
in paragraph (b) of this section as part
of his or her patient assessment in
accordance with the schedule described
in § 412.610. IRFs must also complete a
patient assessment instrument in
accordance with § 412.606 for each
Medicare Part C (Medicare Advantage)
patient admitted to or discharged from
an IRF on or after October 1, 2009.
*
■
■
■
*
*
*
*
6. Section 412.610 is amended by—
A. Revising paragraph (a).
B. Revising paragraph (b).
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C. Revising paragraph (c) introductory
text.
■ D. Revising paragraph (c)(1)(i)(A).
■ E. Revising paragraph (c)(2)(ii)(B).
■ F. Revising paragraph (f).
The revisions read as follows:
■
Subpart P—Prospective Payment for
Inpatient Rehabilitation Hospitals and
Rehabilitation Units
§ 412.606
§ 412.29 Excluded rehabilitation units:
Additional requirements.
*
per week to determine the
appropriateness of treatment.
*
*
*
*
*
§ 412.610
Assessment schedule.
(a) General. For each Medicare Part A
fee-for-service or Medicare Part C
(Medicare Advantage) inpatient, an
inpatient rehabilitation facility must
complete a patient assessment
instrument as specified in § 412.606 that
covers a time period that is in
accordance with the assessment
schedule specified in paragraph (c) of
this section.
(b) Starting the assessment schedule
day count. The first day that the
Medicare Part A fee-for-service or
Medicare Part C (Medicare Advantage)
inpatient is furnished Medicare-covered
services during his or her current
inpatient rehabilitation facility hospital
stay is counted as day one of the patient
assessment schedule.
(c) Assessment schedules and
references dates. The inpatient
rehabilitation facility must complete a
patient assessment instrument upon the
Medicare Part A fee-for-service or
Medicare Part C (Medicare Advantage)
patient’s admission and discharge as
specified in paragraphs (c)(1) and (c)(2)
of this section.
(1) * * *
(i) * * *
(A) Time period is a span of time that
covers calendar days 1 through 3 of the
patient’s current Medicare Part A feefor-service or Medicare Part C (Medicare
Advantage) hospitalization;
*
*
*
*
*
(2) * * *
(ii) * * *
(B) The patient stops being furnished
Medicare Part A fee-for-service or
Medicare Part C (Medicare Advantage)
inpatient rehabilitation services.
*
*
*
*
*
(f) Patient assessment instrument
record retention. An inpatient
rehabilitation facility must maintain all
patient assessment data sets completed
on Medicare Part A fee-for-service
patients within the previous 5 years and
Medicare Part C (Medicare Advantage)
patients within the previous 10 years
either in a paper format in the patient’s
clinical record or in an electronic
computer file format that the inpatient
rehabilitation facility can easily obtain
and produce upon request to CMS or its
contractors.
7. Section 412.614 is amended by—
A. Revising paragraph (a) introductory
text.
■
■
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■
■
■
■
B. Removing paragraph (a)(3).
C. Revising paragraph (b)(1).
D. Revising paragraph (d).
E. Revising paragraph (e).
The revisions read as follows:
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§ 412.614 Transmission of patient
assessment data.
(a) Data format. General rule. The
inpatient rehabilitation facility must
encode and transmit data for each
Medicare Part A fee-for-service and
Medicare Part C (Medicare Advantage)
inpatient—
*
*
*
*
*
(b) * * *
(1) Electronically transmit complete,
accurate, and encoded data from the
patient assessment instrument for each
Medicare Part A fee-for-service and
Medicare Part C (Medicare Advantage)
inpatient to our patient data system in
accordance with the data format
specified in paragraph (a) of this
section; and
*
*
*
*
*
(d) Consequences of failure to submit
complete and timely IRF–PAI data, as
required under paragraph (c) of this
section.
(1) Medicare Part-A fee-for-service
data—
(i) We assess a penalty when an
inpatient rehabilitation facility does not
transmit all of the required data from
the patient assessment instrument for its
Medicare Part A fee-for-service patients
to our patient data system in accordance
with the transmission timeline in
paragraph (c) of this section.
(ii) If the actual patient assessment
data transmission date for a Medicare
Part A fee-for-service patient is later
than 10 calendar days from the
transmission date specified in paragraph
(c) of this section, the patient
assessment data is considered late and
the inpatient rehabilitation facility
receives a payment rate than is 25
percent less than the payment rate
associated with a case-mix group.
(2) Medicare Part C (Medicare
Advantage) data. Failure of the
inpatient rehabilitation facility to
transmit all of the required patient
assessment instrument data for its
Medicare Part C (Medicare Advantage)
patients to our patient data system in
accordance with the transmission
timeline in paragraph (c) of this section
will result in a forfeiture of the facility’s
ability to have any of its Medicare Part
C (Medicare Advantage) data used in the
calculations for determining the
facility’s compliance with the
regulations in § 412.23(b)(2).
(e) Exemption to the consequences for
transmitting the IRF–PAI data late. CMS
may waive the consequences of failure
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to submit complete and timely IRF–PAI
data specified in paragraph (d) of this
section when, due to an extraordinary
situation that is beyond the control of an
inpatient rehabilitation facility, the
inpatient rehabilitation facility is unable
to transmit the patient assessment data
in accordance with paragraph (c) of this
section. Only CMS can determine if a
situation encountered by an inpatient
rehabilitation facility is extraordinary
and qualifies as a situation for waiver of
the penalty specified in paragraph
(d)(1)(ii) of this section or for waiver of
the forfeiture specified in paragraph
(d)(2) of this section. An extraordinary
situation may be due to, but is not
limited to, fires, floods, earthquakes, or
similar unusual events that inflect
extensive damage to an inpatient
facility. An extraordinary situation may
be one that produces a data
transmission problem that is beyond the
control of the inpatient rehabilitation
facility, as well as other situations
determined by CMS to be beyond the
control of the inpatient rehabilitation
facility. An extraordinary situation must
be fully documented by the inpatient
rehabilitation facility.
8. Section 412.618 is amended by
revising the introductory text to read as
follows.
■
§ 412.618 Assessment process for
interrupted stays.
For purposes of the patient
assessment process, if a Medicare Part A
fee-for-service or Medicare Part C
(Medicare Advantage) patient has an
interrupted stay, as defined under
§ 412.602, the following applies:
*
*
*
*
*
■ 9. Section 412.622 is amended by
adding paragraphs (a)(3) through (a)(5)
to read as follows:
§ 412.622
Basis of payment.
(a) * * *
(3) IRF coverage criteria. In order for
an IRF claim to be considered
reasonable and necessary under section
1862(a)(1) of the Act, there must be a
reasonable expectation that the patient
meets all of the following requirements
at the time of the patient’s admission to
the IRF—
(i) Requires the active and ongoing
therapeutic intervention of multiple
therapy disciplines (physical therapy,
occupational therapy, speech-language
pathology, or prosthetics/orthotics
therapy), one of which must be physical
or occupational therapy.
(ii) Generally requires and can
reasonably be expected to actively
participate in, and benefit from, an
intensive rehabilitation therapy
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program. Under current industry
standards, this intensive rehabilitation
therapy program generally consists of at
least 3 hours of therapy (physical
therapy, occupational therapy, speechlanguage pathology, or prosthetics/
orthotics therapy) per day at least 5 days
per week. In certain well-documented
cases, this intensive rehabilitation
therapy program might instead consist
of at least 15 hours of intensive
rehabilitation therapy within a 7
consecutive day period, beginning with
the date of admission to the IRF. Benefit
from this intensive rehabilitation
therapy program is demonstrated by
measurable improvement that will be of
practical value to the patient in
improving the patient’s functional
capacity or adaptation to impairments.
The required therapy treatments must
begin within 36 hours from midnight of
the day of admission to the IRF.
(iii) Is sufficiently stable at the time of
admission to the IRF to be able to
actively participate in the intensive
rehabilitation therapy program that is
described in paragraph (a)(3)(ii) of this
section.
(iv) Requires physician supervision by
a rehabilitation physician, defined as a
licensed physician with specialized
training and experience in inpatient
rehabilitation. The requirement for
medical supervision means that the
rehabilitation physician must conduct
face-to-face visits with the patient at
least 3 days per week throughout the
patient’s stay in the IRF to assess the
patient both medically and functionally,
as well as to modify the course of
treatment as needed to maximize the
patient’s capacity to benefit from the
rehabilitation process.
(4) Documentation. To document that
each patient for whom the IRF seeks
payment is reasonably expected to meet
all of the requirements in paragraph
(a)(3) of this section at the time of
admission, the patient’s medical record
at the IRF must contain the following
documentation—
(i) A comprehensive preadmission
screening that meets all of the following
requirements—
(A) It is conducted by a licensed or
certified clinician(s) designated by a
rehabilitation physician described in
paragraph (a)(3)(iv) of this section
within the 48 hours immediately
preceding the IRF admission. A
preadmission screening that includes all
of the required elements, but that is
conducted more than 48 hours
immediately preceding the IRF
admission, will be accepted as long as
an update is conducted in person or by
telephone to update the patient’s
medical and functional status within the
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48 hours immediately preceding the IRF
admission and is documented in the
patient’s medical record.
(B) It includes a detailed and
comprehensive review of each patient’s
condition and medical history.
(C) It serves as the basis for the initial
determination of whether or not the
patient meets the requirements for an
IRF admission to be considered
reasonable and necessary in paragraph
(a)(3) of this section.
(D) It is used to inform a rehabilitation
physician who reviews and documents
his or her concurrence with the findings
and results of the preadmission
screening.
(E) It is retained in the patient’s
medical record at the IRF.
(ii) A post-admission physician
evaluation that meets all of the
following requirements—
(A) It is completed by a rehabilitation
physician within 24 hours of the
patient’s admission to the IRF.
(B) It documents the patient’s status
on admission to the IRF, includes a
comparison with the information noted
in the preadmission screening
documentation, and serves as the basis
for the development of the overall
individualized plan of care.
(C) It is retained in the patient’s
medical record at the IRF.
(iii) An individualized overall plan of
care for the patient that meets all of the
following requirements—
(A) It is developed by a rehabilitation
physician, as defined in paragraph
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(a)(3)(iv) of this section, with input from
the interdisciplinary team within 4 days
of the patient’s admission to the IRF.
(B) It is retained in the patient’s
medical record at the IRF.
(5) Interdisciplinary team approach to
care. In order for an IRF claim to be
considered reasonable and necessary
under section 1862(a)(1) of the Act, the
patient must require an
interdisciplinary team approach to care,
as evidenced by documentation in the
patient’s medical record of weekly
interdisciplinary team meetings that
meet all of the following requirements—
(A) The team meetings are led by a
rehabilitation physician as defined in
paragraph (a)(3)(iv) of this section, and
further consist of a registered nurse with
specialized training or experience in
rehabilitation; a social worker or case
manager (or both); and a licensed or
certified therapist from each therapy
discipline involved in treating the
patient. All team members must have
current knowledge of the patient’s
medical and functional status.
(B) The team meetings occur at least
once per week throughout the duration
of the patient’s stay to implement
appropriate treatment services; review
the patient’s progress toward stated
rehabilitation goals; identify any
problems that could impede progress
towards those goals; and, where
necessary, reassess previously
established goals in light of
impediments, revise the treatment plan
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in light of new goals, and monitor
continued progress toward those goals.
(C) The results and findings of the
team meetings, and the concurrence by
the rehabilitation physician with those
results and findings, are retained in the
patient’s medical record.
Authority: (Catalog of Federal Domestic
Assistance Program No. 93.773, Medicare—
Hospital Insurance; and Program No. 93.774,
Medicare—Supplementary Medical
Insurance Program).
Dated: July 20, 2009.
Charlene Frizzera,
Acting Administrator, Centers for Medicare
& Medicaid Services.
Approved: July 30, 2009.
Kathleen Sebelius,
Secretary.
The following addendum will not
appear in the Code of Federal
Regulations.
Addendum
In this addendum, we provide the
wage index tables referred to throughout
the preamble to this proposed rule. The
tables presented below are as follows:
Table 1.—Inpatient Rehabilitation
Facility Wage Index for Urban Areas for
Discharges Occurring from October 1,
2009 through September 30, 2010
Table 2.—Inpatient Rehabilitation
Facility Wage Index for Rural Areas for
Discharges Occurring from October 1,
2009 through September 30, 2010
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Agencies
[Federal Register Volume 74, Number 151 (Friday, August 7, 2009)]
[Rules and Regulations]
[Pages 39762-39838]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-18616]
[[Page 39761]]
-----------------------------------------------------------------------
Part III
Department of Health and Human Services
-----------------------------------------------------------------------
Centers for Medicare & Medicaid Services
-----------------------------------------------------------------------
42 CFR Part 412
Medicare Program; Inpatient Rehabilitation Facility Prospective Payment
System for Federal Fiscal Year 2010; Final Rule
Federal Register / Vol. 74, No. 151 / Friday, August 7, 2009 / Rules
and Regulations
[[Page 39762]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 412
[CMS-1538-F]
RIN 0938-AP56
Medicare Program; Inpatient Rehabilitation Facility Prospective
Payment System for Federal Fiscal Year 2010
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This final rule updates the payment rates for inpatient
rehabilitation facilities (IRFs) for Federal fiscal year (FY) 2010 (for
discharges occurring on or after October 1, 2009 and on or before
September 30, 2010) as required under section 1886(j)(3)(C) of the
Social Security Act (the Act). Section 1886(j)(5) of the Act requires
the Secretary to publish in the Federal Register on or before the
August 1 that precedes the start of each fiscal year, the
classification and weighting factors for the IRF prospective payment
system's (PPS) case-mix groups and a description of the methodology and
data used in computing the prospective payment rates for that fiscal
year.
We are revising existing policies regarding the IRF PPS within the
authority granted under section 1886(j) of the Act.
DATES: Effective Date. The provisions of the final rule are effective
October 1, 2009, except for the amendments to Sec. 412.23, Sec.
412.29, and Sec. 412.622 which are effective January 1, 2010.
Applicability Date. The amendments to Sec. 412.23, Sec. 412.29,
and Sec. 412.622 are applicable to IRF discharges occurring on or
after January 1, 2010. The updated IRF prospective payment rates are
applicable for IRF discharges occurring on or after October 1, 2009 and
on or before September 30, 2010 (FY 2010).
FOR FURTHER INFORMATION CONTACT: Susanne Seagrave, (410) 786-0044, for
information regarding the payment policies.
Julie Stankivic, (410) 786-5725, for general information regarding
the proposed rule.
Jeanette Kranacs, (410) 786-9385, for information regarding the
wage index.
SUPPLEMENTARY INFORMATION:
Table of Contents
I. Background
A. Historical Overview of the Inpatient Rehabilitation Facility
Prospective Payment System (IRF PPS)
B. Operational Overview of the Current IRF PPS
II. Summary of Provisions of the Proposed Rule
A. Proposed Updates to the IRF PPS for Federal Fiscal Year (FY)
2010
B. Proposed Revisions to Existing Regulation Text
C. Proposed New Regulation Text
D. Proposed Rescission of Outdated HCFAR-85-2-1
III. Analysis of and Responses to Public Comments
IV. Update to the Case-Mix Group (CMG) Relative Weights and Average
Length of Stay Values for FY 2010
V. Updates to the Facility-Level Adjustment Factors for FY 2010
A. Updates to the Adjustment Factors for FY 2010
B. Budget Neutrality Methodology for the Updates to the IRF
Facility-Level Adjustment Factors
VI. FY 2010 IRF PPS Federal Prospective Payment Rates
A. Market Basket Increase Factor and Labor-Related Share for FY
2010
B. Area Wage Adjustment
C. Description of the Final IRF Standard Payment Conversion
Factor and Payment Rates for FY 2010
D. Example of the Methodology for Adjusting the Federal
Prospective Payment Rates
VII. Update to Payments for High-Cost Outliers Under the IRF PPS
A. Update to the Outlier Threshold Amount for FY 2010
B. Update to the IRF Cost-to-Charge Ratio Ceilings
VIII. Inpatient Rehabilitation Facility (IRF) Coverage Requirements
A. Requirements for the Preadmission Screening
B. Requirement for a Post-Admission Physician Evaluation
C. Requirement for an Individualized Overall Plan of Care
D. Requirements for Evaluating the Appropriateness of an IRF
Admission
E. Requirements for the Interdisciplinary Team Meetings
F. Requirement for Physician Supervision
G. Requirement Regarding Initiation of Therapy Services
H. Provision of Group Therapies in IRFs
I. Clarifying and Conforming Amendments
J. HCFAR 85-2 Ruling
IX. Revisions to the Regulation Text To Require IRFs To Submit
Patient Assessments on Medicare Advantage Patients for Use in the
``60 Percent Rule'' Calculations
A. Background on the ``60 Percent Rule'' Calculations
B. Requirement To Submit Assessment Data on Medicare Advantage
Patients
X. Miscellaneous Comments
XI. Provisions of the Final Rule
A. Payment Provision Changes
B. Regulatory Text Changes
XII. Collection of Information Requirements
XIII. Regulatory Impact Analysis
A. Overall Impact
B. Anticipated Effects of the Final Rule
C. Alternatives Considered
D. Accounting Statement
E. Conclusion
Regulation Text
Addendum
Acronyms
Because of the many terms to which we refer by acronym in this
final rule, we are listing the acronyms used and their corresponding
terms in alphabetical order below.
ADC Average Daily Census
ASCA Administrative Simplification Compliance Act, Public Law 107-
105
BBA Balanced Budget Act of 1997, Public Law 105-33
BBRA Medicare, Medicaid, and SCHIP [State Children's Health
Insurance Program] Balanced Budget Refinement Act of 1999, Public
Law 106-113
BIPA Medicare, Medicaid, and SCHIP [State Children's Health
Insurance Program] Benefits Improvement and Protection Act of 2000,
Public Law 106-554
CBSA Core-Based Statistical Area
CCR Cost-to-Charge Ratio
CFR Code of Federal Regulations
CMG Case-Mix Group
DRG Diagnostic Related Group
DSH Disproportionate Share Hospital
FI Fiscal Intermediary
FR Federal Register
FTE Full-time Equivalent
FY Federal Fiscal Year
HCFA Health Care Financing Administration
HHH Hubert H. Humphrey Building
HIPAA Health Insurance Portability and Accountability Act, Public
Law 104-191
IOM Internet Only Manual
IPF Inpatient Psychiatric Facility
IPPS Inpatient Prospective Payment System
IRF Inpatient Rehabilitation Facility
IRF-PAI Inpatient Rehabilitation Facility--Patient Assessment
Instrument
IRF PPS Inpatient Rehabilitation Facility Prospective Payment System
IRVEN Inpatient Rehabilitation Validation and Entry
LTCH Long Term Care Hospital
LIP Low-Income Percentage
MA Medicare Advantage
MAC Medicare Administrative Contractor
MBPM Medicare Benefit Policy Manual
MMSEA Medicare, Medicaid, and SCHIP Extension Act of 2007, Public
Law 110-173
OMB Office of Management and Budget
PAI Patient Assessment Instrument
PPS Prospective Payment System
QIC Qualified Independent Contractors
RAC Recovery Audit Contractors
RAND RAND Corporation
RFA Regulatory Flexibility Act, Public Law 96-354
RIA Regulatory Impact Analysis
RIC Rehabilitation Impairment Category
RPL Rehabilitation, Psychiatric, and Long-Term Care Hospital Market
Basket
SCHIP State Children's Health Insurance Program
[[Page 39763]]
I. Background
A. Historical Overview of the Inpatient Rehabilitation Facility
Prospective Payment System (IRF PPS)
Section 4421 of the Balanced Budget Act of 1997 (BBA), Public Law
105-33, as amended by section 125 of the Medicare, Medicaid, and SCHIP
(State Children's Health Insurance Program) Balanced Budget Refinement
Act of 1999 (BBRA), Public Law 106-113, and by section 305 of the
Medicare, Medicaid, and SCHIP Benefits Improvement and Protection Act
of 2000 (BIPA), Public Law 106-554, provides for the implementation of
a per discharge prospective payment system (PPS) under section 1886(j)
of the Social Security Act (the Act) for inpatient rehabilitation
hospitals and inpatient rehabilitation units of a hospital (hereinafter
referred to as IRFs).
Payments under the IRF PPS encompass inpatient operating and
capital costs of furnishing covered rehabilitation services (that is,
routine, ancillary, and capital costs) but not direct graduate medical
education costs, costs of approved nursing and allied health education
activities, bad debts, and other services or items outside the scope of
the IRF PPS. Although a complete discussion of the IRF PPS provisions
appears in the original FY 2002 IRF PPS final rule (66 FR 41316) and
the FY 2006 IRF PPS final rule (70 FR 47880), we are providing below a
general description of the IRF PPS for fiscal years (FYs) 2002 through
2009.
Under the IRF PPS from FY 2002 through FY 2005, as described in the
FY 2002 IRF PPS final rule (66 FR 41316), the Federal prospective
payment rates were computed across 100 distinct case-mix groups (CMGs).
We constructed 95 CMGs using rehabilitation impairment categories
(RICs), functional status (both motor and cognitive), and age (in some
cases, cognitive status and age may not be a factor in defining a CMG).
In addition, we constructed five special CMGs to account for very short
stays and for patients who expire in the IRF.
For each of the CMGs, we developed relative weighting factors to
account for a patient's clinical characteristics and expected resource
needs. Thus, the weighting factors accounted for the relative
difference in resource use across all CMGs. Within each CMG, we created
tiers based on the estimated effects that certain comorbidities would
have on resource use.
We established the Federal PPS rates using a standardized payment
conversion factor (formerly referred to as the budget neutral
conversion factor). For a detailed discussion of the budget neutral
conversion factor, please refer to our FY 2004 IRF PPS final rule (68
FR 45684 through 45685). In the FY 2006 IRF PPS final rule (70 FR
47880), we discussed in detail the methodology for determining the
standard payment conversion factor.
We applied the relative weighting factors to the standard payment
conversion factor to compute the unadjusted Federal prospective payment
rates under the IRF PPS from FYs 2002 through 2005. Within the
structure of the payment system, we then made adjustments to account
for interrupted stays, transfers, short stays, and deaths. Finally, we
applied the applicable adjustments to account for geographic variations
in wages (wage index), the percentage of low-income patients, location
in a rural area (if applicable), and outlier payments (if applicable)
to the IRF's unadjusted Federal prospective payment rates.
For cost reporting periods that began on or after January 1, 2002
and before October 1, 2002, we determined the final prospective payment
amounts using the transition methodology prescribed in section
1886(j)(1) of the Act. Under this provision, IRFs transitioning into
the PPS were paid a blend of the Federal IRF PPS rate and the payment
that the IRF would have received had the IRF PPS not been implemented.
This provision also allowed IRFs to elect to bypass this blended
payment and immediately be paid 100 percent of the Federal IRF PPS
rate. The transition methodology expired as of cost reporting periods
beginning on or after October 1, 2002 (FY 2003), and payments for all
IRFs now consist of 100 percent of the Federal IRF PPS rate.
We established a CMS Web site as a primary information resource for
the IRF PPS. The Web site URL is https://www.cms.hhs.gov/InpatientRehabFacPPS/ and may be accessed to download or view
publications, software, data specifications, educational materials, and
other information pertinent to the IRF PPS.
Section 1886(j) of the Act confers broad statutory authority upon
the Secretary to propose refinements to the IRF PPS. In the FY 2006 IRF
PPS final rule (70 FR 47880) and in correcting amendments to the FY
2006 IRF PPS final rule (70 FR 57166) that we published on September
30, 2005, we finalized a number of refinements to the IRF PPS case-mix
classification system (the CMGs and the corresponding relative weights)
and the case-level and facility-level adjustments. These refinements
included the adoption of OMB's Core-Based Statistical Area (CBSA)
market definitions, modifications to the CMGs, tier comorbidities, and
CMG relative weights, implementation of a new teaching status
adjustment for IRFs, revision and rebasing of the IRF market basket,
and updates to the rural, low-income percentage (LIP), and high-cost
outlier adjustments. Any reference to the FY 2006 IRF PPS final rule in
this proposed rule also includes the provisions effective in the
correcting amendments. For a detailed discussion of the final key
policy changes for FY 2006, please refer to the FY 2006 IRF PPS final
rule (70 FR 47880 and 70 FR 57166).
In the FY 2007 IRF PPS final rule (71 FR 48354), we further refined
the IRF PPS case-mix classification system (the CMG relative weights)
and the case-level adjustments, to ensure that IRF PPS payments would
continue to reflect as accurately as possible the costs of care. For a
detailed discussion of the FY 2007 policy revisions, please refer to
the FY 2007 IRF PPS final rule (71 FR 48354).
In the FY 2008 IRF PPS final rule (72 FR 44284), we updated the
Federal prospective payment rates and the outlier threshold, revised
the IRF wage index policy, and clarified how we determine high-cost
outlier payments for transfer cases. For more information on the policy
changes implemented for FY 2008, please refer to the FY 2008 IRF PPS
final rule (72 FR 44284), in which we published the final FY 2008 IRF
Federal prospective payment rates.
After publication of the FY 2008 IRF PPS final rule (72 FR 44284),
section 115 of the Medicare, Medicaid, and SCHIP Extension Act of 2007,
Public Law 110-173 (MMSEA), amended section 1886(j)(3)(C) of the Act to
apply a zero percent increase factor for FYs 2008 and 2009, effective
for IRF discharges occurring on or after April 1, 2008. Section
1886(j)(3)(C) of the Act requires the Secretary to develop an increase
factor to update the IRF Federal prospective payment rates for each FY.
Based on the legislative change to the increase factor, we revised the
FY 2008 Federal prospective payment rates for IRF discharges occurring
on or after April 1, 2008. Thus, the final FY 2008 IRF Federal
prospective payment rates that were published in the FY 2008 IRF PPS
final rule (72 FR 44284) were effective for discharges occurring on or
after October 1, 2007 and on or before March 31, 2008; and the revised
FY 2008 IRF Federal prospective payment rates were effective for
discharges occurring on or after April 1, 2008 and on or before
September 30, 2008. The
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revised FY 2008 Federal prospective payment rates are available on the
CMS Web site at https://www.cms.hhs.gov/InpatientRehabFacPPS/07_DataFiles.asp#TopOfPage.
In the FY 2009 IRF PPS final rule (73 FR 46370), we updated the CMG
relative weights, the average length of stay values, and the outlier
threshold; clarified IRF wage index policies regarding the treatment of
``New England deemed'' counties and multi-campus hospitals; and revised
the regulation text in response to section 115 of the MMSEA to set the
IRF compliance percentage at 60 percent (``the 60 percent rule'') and
continue the practice of including comorbidities in the calculation of
compliance percentages. We also applied a zero percent increase factor
for FY 2009. For more information on the policy changes implemented for
FY 2009, please refer to the FY 2009 IRF PPS final rule (73 FR 46370),
in which we published the final FY 2009 IRF Federal prospective payment
rates.
B. Operational Overview of the Current IRF PPS
As described in the FY 2002 IRF PPS final rule, upon the admission
and discharge of a Medicare Part A fee-for-service patient, the IRF is
required to complete the appropriate sections of a patient assessment
instrument (PAI), the Inpatient Rehabilitation Facility-Patient
Assessment Instrument (IRF-PAI). All required data must be
electronically encoded into the IRF-PAI software product. Generally,
the software product includes patient classification programming called
the GROUPER software. The GROUPER software uses specific IRF-PAI data
elements to classify (or group) patients into distinct CMGs and account
for the existence of any relevant comorbidities.
The GROUPER software produces a five-digit CMG number. The first
digit is an alpha-character that indicates the comorbidity tier. The
last four digits represent the distinct CMG number. Free downloads of
the Inpatient Rehabilitation Validation and Entry (IRVEN) software
product, including the GROUPER software, are available on the CMS Web
site at https://www.cms.hhs.gov/InpatientRehabFacPPS/06_Software.asp.
Once a patient is discharged, the IRF submits a Medicare claim as a
Health Insurance Portability and Accountability Act (HIPAA), Public Law
104-191, compliant electronic claim or, if the Administrative
Simplification Compliance Act (ASCA), Public Law 107-105, permits, a
paper claim (a UB-04 or a CMS-1450 as appropriate) using the five-digit
CMG number and sends it to the appropriate Medicare fiscal intermediary
(FI) or Medicare Administrative Contractor (MAC). Claims submitted to
Medicare must comply with both ASCA and HIPAA.
Section 3 of the ASCA amends section 1862(a) of the Act by adding
paragraph (22) which requires the Medicare program, subject to section
1862(h) of the Act, to deny payment under Part A or Part B for any
expenses for items or services ``for which a claim is submitted other
than in an electronic form specified by the Secretary.'' Section
1862(h) of the Act, in turn, provides that the Secretary shall waive
such denial in situations in which there is no method available for the
submission of claims in an electronic form or the entity submitting the
claim is a small provider. In addition, the Secretary also has the
authority to waive such denial ``in such unusual cases as the Secretary
finds appropriate.'' For more information we refer the reader to the
final rule, ``Medicare Program; Electronic Submission of Medicare
Claims'' (70 FR 71008, November 25, 2005). CMS instructions for the
limited number of Medicare claims submitted on paper are available at:
https://www.cms.hhs.gov/manuals/downloads/clm104c25.pdf.
Section 3 of the ASCA operates in the context of the administrative
simplification provisions of HIPAA, which include, among others, the
requirements for transaction standards and code sets codified in 45 CFR
parts 160 and 162, subparts A and I through R (generally known as the
Transactions Rule). The Transactions Rule requires covered entities,
including covered healthcare providers, to conduct covered electronic
transactions according to the applicable transaction standards. (See
the program claim memoranda issued and published by CMS at: https://www.cms.hhs.gov/ElectronicBillingEDITrans/ and listed in the addenda to
the Medicare Intermediary Manual, Part 3, section 3600).
The Medicare FI or MAC processes the claim through its software
system. This software system includes pricing programming called the
``PRICER'' software. The PRICER software uses the CMG number, along
with other specific claim data elements and provider-specific data, to
adjust the IRF's prospective payment for interrupted stays, transfers,
short stays, and deaths, and then applies the applicable adjustments to
account for the IRF's wage index, percentage of low-income patients,
rural location, and outlier payments. For discharges occurring on or
after October 1, 2005, the IRF PPS payment also reflects the new
teaching status adjustment that became effective as of FY 2006, as
discussed in the FY 2006 IRF PPS final rule (70 FR 47880).
II. Summary of Provisions of the Proposed Rule
As discussed in the FY 2010 IRF PPS proposed rule (74 FR 21052), we
proposed updates to the IRF PPS, revisions to existing regulations text
for the purpose of providing greater clarity, new regulations text to
improve calculation of compliance with the ``60 percent'' rule, and
rescission of an outdated Health Care Financing Administration (HFCA)
Ruling (HCFAR 85-2-1). These proposals are as follows:
A. Proposed Updates to the IRF PPS for Federal Fiscal Year (FY) 2010
Update the FY 2010 IRF PPS relative weights and average
length of stay values using the most current and complete Medicare
claims and cost report data in a budget neutral manner, as discussed in
section III of the FY 2010 IRF PPS proposed rule (74 FR 21052, 21055
through 21059).
Update the FY 2010 IRF facility-level adjustments (rural,
LIP, and teaching status adjustments) using the most current and
complete Medicare claims and cost report data in a budget neutral
manner, as discussed in section IV of the FY 2010 IRF PPS proposed rule
(74 FR 21052, 21059 through 21062).
Update the FY 2010 IRF PPS payment rates by the proposed
market basket, as discussed in section V.A of the FY 2010 IRF PPS
proposed rule (74 FR 21052 at 21062).
Update the FY 2010 IRF PPS payment rates by the proposed
wage index and the labor-related share in a budget neutral manner, as
discussed in section V.A and V.B of the FY 2010 IRF PPS proposed rule
(74 FR 21052, 21062 through 21063).
Update the outlier threshold amount for FY 2010, as
discussed in section VI.A of the FY 2010 IRF PPS proposed rule (74 FR
21052 at 21066).
B. Proposed Revisions to Existing Regulation Text
Relocate and revise the criteria for admission to an
inpatient rehabilitation hospital found at existing Sec. 412.23(b)(3)
through (b)(7) that describe requirements relating to preadmission
screening, close medical supervision, a director of rehabilitation, the
plan of care, and a coordinated multidisciplinary team approach.
Redesignate paragraphs (b)(8) and (b)(9) of Sec. 412.23 as paragraphs
(b)(3) and
[[Page 39765]]
(b)(4) and revise newly redesignated paragraph (b)(4), as described in
section VII of the FY 2010 IRF PPS proposed rule (74 FR 21052, 21067
through 21071).
Revise the section heading at Sec. 412.29 to include
inpatient rehabilitation hospitals, as described in section VII of the
FY 2010 IRF PPS proposed rule (74 FR 21052, 21067 through 21071).
Relocate and revise the existing requirements at Sec.
412.29(b) through (f) that describe the admission requirements relating
to preadmission screening, close medical supervision, a director of
rehabilitation, the plan of care, and a coordinated multidisciplinary
team approach, as described in section VII of the FY 2010 IRF PPS
proposed rule (74 FR 21052, 21067 through 21071).
Revise the section heading at Sec. 412.30, as described
in section VII of the FY 2010 IRF PPS proposed rule (74 FR 21052, 21067
through 21071).
Revise the regulation text in Sec. 412.604, Sec.
412.606, Sec. 412.610. Sec. 412.614 and Sec. 412.618 to require the
collection of inpatient rehabilitation facility patient assessment
instrument data on Medicare Part C (Medicare Advantage) patients in
IRFs for use in the 60 percent rule compliance percentage calculations,
as described in section VIII of the FY 2010 IRF PPS proposed rule (74
FR 21052, 21071 through 21073).
Remove Sec. 412.614(a)(3) that provides for an exception
in the transmission of IRF-PAI data to CMS, as described in section
VIII of the FY 2010 IRF PPS proposed rule (74 FR 21052, 21071 through
21073).
Revise the heading at Sec. 412.614(d) to ``Consequences
of failure to submit complete and timely IRF-PAI data, as required
under paragraph (c) of this section,'' as described in section VIII of
the FY 2010 IRF PPS proposed rule (74 FR 21052, 21071 through 21073).
Revise the heading at Sec. 412.614(d)(1) to ``Medicare
Part A fee-for-service data,'' as described in section VIII of the FY
2010 IRF PPS proposed rule (74 FR 21052, 21071 through 21073).
Make a technical correction to the paragraph formerly
designated as Sec. 412.614(d)(1) and assign the revised language to a
new paragraph Sec. 412.614(d)(1)(a), as described in section VIII of
the FY 2010 IRF PPS proposed rule (74 FR 21052, 21071 through 21073).
Redesignate paragraph Sec. 412.614(d)(2) as Sec.
412.614(d)(1)(b), as described in section VIII of the FY 2010 IRF PPS
proposed rule (74 FR 21052, 21071 through 21073).
C. Proposed New Regulation Text
Revise Sec. 412.29, as described in section VII of the FY
2010 IRF PPS proposed rule (74 FR 21052, 21067 through 21071), to
include the requirements for admission to an IRF.
Add a new introductory paragraph at Sec. 412.30 that
includes the requirements previously found in Sec. 412.29(a)
(describing the admission requirements for new and converted
rehabilitation units), as described in section VII of the FY 2010 IRF
PPS proposed rule (74 FR 21052, 21067 through 21071).
Revise Sec. 412.610(f) to require that the IRF provide a
copy of the electronic computer file format of the IRF-PAI to the
contractor upon request, as described in section VII of the FY 2010 IRF
PPS proposed rule (74 FR 21052, 21067 through 21071).
Add a new paragraph Sec. 412.614(d)(2) to indicate that
failure of an IRF to submit IRF-PAI data on all of its Medicare Part C
(Medicare Advantage) patients will result in forfeiture of the IRF's
ability to have any of its Medicare Part C (Medicare Advantage) data
used in the compliance calculations, as described in section VIII of
the FY 2010 IRF PPS proposed rule (74 FR 21052, 21071 through 21073).
D. Proposed Rescission of Outdated HCFAR-85-2-1
Rescind HCFA Ruling 85-2-1 entitled ``Medicare Criteria for
Medicare Coverage of Inpatient Hospital Rehabilitation Services'' and
set forth new coverage guidance to implement the new regulations
adopted under this final rule, as described in section VII of the FY
2010 IRF PPS proposed rule (74 FR 21052 at 21071).
III. Analysis of and Responses to Public Comments
We received approximately 686 timely responses, many of which
contained multiple comments on the FY 2010 IRF PPS proposed rule (74 FR
21052) from the public. We received comments from various trade
associations, inpatient rehabilitation facilities, individual
physicians, therapists, clinicians, health care industry organizations,
and health care consulting firms. The following section, arranged by
subject area, includes a summary of the public comments that we
received, and our responses.
IV. Update to the Case-Mix Group (CMG) Relative Weights and Average
Length of Stay Values for FY 2010
As specified in 42 CFR 412.620(b)(1), we calculate a relative
weight for each CMG that is proportional to the resources needed by an
average inpatient rehabilitation case in that CMG. For example, cases
in a CMG with a relative weight of 2, on average, will cost twice as
much as cases in a CMG with a relative weight of 1. Relative weights
account for the variance in cost per discharge due to the variance in
resource utilization among the payment groups, and their use helps to
ensure that IRF PPS payments support beneficiary access to care as well
as provider efficiency.
In the FY 2010 IRF PPS proposed rule (74 FR 21052, 21055 through
21059), we proposed to update the CMG relative weights and average
length of stay values for FY 2010 using the most recent available data
(at that time, FY 2007 IRF claims and cost report data) to ensure that
IRF PPS payments fully reflect recent changes in IRF utilization due to
the 60 percent rule and medical review activities. To ensure that IRF
PPS payments continue to reflect as accurately as possible the current
costs of care in IRFs, we are updating the CMG relative weights and
average length of stay values for FY 2010 in this final rule using FY
2008 IRF claims and FY 2007 IRF cost report data. These data are the
most current and complete data available at this time. At this time,
only about 20 percent of the FY 2008 IRF cost report data are available
for analysis, but the majority of the FY 2008 IRF claims data are
available for analysis.
We have used the same methodology that we used to update the CMG
relative weights and average length of stay values in the FY 2009 IRF
PPS final rule (73 FR 46370). In calculating the CMG relative weights,
we use a hospital-specific relative value method to estimate operating
(routine and ancillary services) and capital costs of IRFs. The process
used to calculate the CMG relative weights for this final rule follows
below:
Step 1. We calculate the CMG relative weights by estimating the
effects that comorbidities have on costs.
Step 2. We adjust the cost of each Medicare discharge (case) to
reflect the effects found in the first step.
Step 3. We use the adjusted costs from the second step to calculate
CMG relative weights, using the hospital-specific relative value
method.
Step 4. We normalize the FY 2010 CMG relative weights to the same
average CMG relative weight from the
[[Page 39766]]
CMG relative weights implemented in the FY 2009 IRF PPS final rule (73
FR 46370).
Consistent with the way we implemented changes to the IRF
classification system in the FY 2006 IRF PPS final rule (70 FR 47880
and 70 FR 57166), the FY 2007 IRF PPS final rule (71 FR 48354), and the
FY 2009 IRF PPS final rule (73 FR 46370), we are revising the CMG
relative weights for FY 2010 in such a way that total estimated
aggregate payments to IRFs for FY 2010 are estimated to be the same
with or without the changes (that is, in a budget neutral manner) by
applying a budget neutrality factor to the standard payment amount. To
calculate the appropriate budget neutrality factor for use in updating
the FY 2010 CMG relative weights, we use the following steps:
Step 1. Calculate the estimated total amount of IRF PPS payments
for FY 2010 (with no changes to the CMG relative weights).
Step 2. Apply the changes to the CMG relative weights (as discussed
above) to calculate the estimated total amount of IRF PPS payments for
FY 2010.
Step 3. Divide the amount calculated in step 1 by the amount
calculated in step 2 to determine the budget neutrality factor (1.0020)
that maintains the same total estimated aggregate payments in FY 2010
with and without the changes to the CMG relative weights.
Step 4. Apply the budget neutrality factor (1.0020) to the FY 2009
IRF PPS standard payment amount after the application of the budget-
neutral wage adjustment factor.
In section VI.C of this final rule, we discuss the methodology for
calculating the standard payment conversion factor for FY 2010.
Note that the budget neutrality factor that we use to update the
CMG relative weights for FY 2010 changed from 1.0004 in the proposed
rule to 1.0020 in this final rule due to the use of updated FY 2008 IRF
claims data in this final rule.
We received 7 comments on the proposed updates to the CMG relative
weights and average length of stay values, which are summarized below.
Comment: The vast majority of commenters supported the proposed
update to the CMG relative weights and average length of stay values.
However, most suggested that CMS use FY 2008 IRF claims and cost report
data in updating the CMG relative weights and average length of stay
values for the final rule, saying that the effects of recent changes in
the 60 percent rule and the IRF medical necessity review activities are
continuing to be realized through FY 2008 and early FY 2009. Several
commenters said that we should continue to update the CMG relative
weights and average length of stay values annually to reflect changes
in IRF costs and utilization that occur over time.
Response: We appreciate the commenters' suggestions for updating
the data used in the analysis of the CMG relative weights for FY 2010,
and we agree that we should continue to use the most recent available
data for our analyses of the CMG relative weights. However, only about
20 percent of the FY 2008 IRF cost reports are available for analysis
at this time, and we do not believe that 20 percent is a large enough
or representative enough sample of all IRFs on which to base our
updates. Thus, for this final rule, we have continued to use the most
recent available data, which are the FY 2008 IRF claims and FY 2007 IRF
cost report data. We will continue to update the CMG relative weights
and average length of stay values in the future, as appropriate, using
the most recent available data.
Comment: One commenter requested that CMS seek additional sources
of cost information, such as the Cost Resource Utilization (CRU) Tool
data from the Post Acute Care Payment Reform Demonstration (PAC PRD),
to address issues of relative weight compression in future updates to
the CMG relative weights.
Response: We appreciate the commenter's suggestion, and will
consider this suggestion for future analyses once the CRU data are
complete and available for analysis.
Comment: One commenter stated a concern that the proposed update to
the CMG relative weights for FY 2010 would result in a slight decrease
in the average payment per case for IRFs and would increase payments
for certain diagnoses while decreasing payments for other diagnoses.
Response: Consistent with the way that we applied updates to the
CMG relative weights and average length of stay values in the FY 2006
IRF PPS final rule (70 FR 47880 and 70 FR 57166), the FY 2007 IRF PPS
final rule (71 FR 48354), and the FY 2009 IRF PPS final rule (73 FR
46370), we are updating the CMG relative weights and average length of
stay values in this final rule in a budget-neutral manner, so that
estimated aggregate payments to IRFs do not increase or decrease as a
result of these updates. Thus, we apply a budget-neutrality factor of
1.0020 to increase the standard payment conversion factor (as described
in section VI.C of this final rule) to counteract any estimated
decrease in aggregate IRF payments as a result of the updates to the
CMG relative weights and average length of stay values.
Further, as we stated in the FY 2010 IRF PPS proposed rule (74 FR
21052 at 21059), the updates are generally expected to result in some
increases and some decreases to the CMG relative weight values. Changes
in the relative weights are, by definition, distributional and,
therefore, the fact that the updates shown in Table 1 increase IRF
payments to some diagnoses and decrease IRF payments to other diagnoses
is to be expected. The intent of these changes is to ensure that the
relative payments assigned to the CMGs and tiers continue to reflect
the relative costs of caring for different types of patients in IRFs.
Comment: Several commenters requested that we reiterate that the
average length of stay values are not intended to be used as clinical
guidelines for patient care, but are only used to determine when an IRF
discharge meets the definition of a short-stay transfer, which results
in a per diem case level adjustment.
Response: We agree with this comment, and we already stated that
the purpose of the average length of stay values is to determine when
an IRF discharge meets the definition of a short-stay transfer in the
FY 2010 IRF PPS proposed rule (74 FR 21052 at 21056). As the commenter
notes, the average length of stay values are not intended to be used as
clinical guidelines for patient care.
Comment: One commenter suggested that we consider alternative
methodologies for updating the CMG relative weights in the future to
improve their ability to predict IRFs' cost per case, and expressed a
concern about the need to update the weighted motor score methodology
used to classify IRF patients into CMGs that was finalized in the FY
2006 IRF PPS final rule (70 FR 47880 at 47900).
Response: We appreciate the commenter's suggestions regarding
alternative methodologies for analyzing future updates to the CMG
relative weights, and will review them carefully. We will also take
into account the commenter's suggestion that we update the weights used
in the motor score calculation in the future.
Final Decision: After carefully considering all of the comments
that we received on the proposed updates to the CMG relative weights
and average length of stay values, we are implementing the FY 2010
updates to the CMG relative weights and average length of stay values
presented in Table
[[Page 39767]]
1 below (which are different from the relative weights and average
length of stay values that we had proposed because these final values
are based on analysis of updated FY 2008 data).
BILLING CODE 4120-01-P
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BILLING CODE 4120-01-C
V. Updates to the Facility-Level Adjustment Factors for FY 2010
A. Updates to the Adjustment Factors for FY 2010
Section 1886(j)(3)(A)(v) of the Act confers broad authority upon
the Secretary to adjust the per unit payment rate ``by such * * *
factors as the Secretary determines are necessary to properly reflect
variations in necessary costs of treatment among rehabilitation
facilities.'' For example, we adjust the Federal prospective payment
amount associated with a CMG to account for facility-level
characteristics such as an IRF's LIP percentage, teaching status, and
location in a rural area, if applicable, as described in Sec.
412.624(e).
In the FY 2010 IRF PPS proposed rule (74 FR 21052, 21059 through
21062), we proposed to update the adjustment factors for calculating
the rural, LIP, and teaching status adjustments based on the most
recent three years worth of IRF claims data (at that time, FY 2005, FY
2006, and FY 2007) and the most recent available corresponding IRF cost
report data. Note that, for each IRF claim, we used the corresponding
year's cost report data, when available. In the rare instances in which
the corresponding year's cost report data were not available, we used
the most recent available cost report data. For example, since cost
report years are determined by the start date of the cost report, a
hypothetical IRF's cost reporting period from July 1, 2007 through June
30, 2008 would be referred to as an ``FY 2007'' cost report. However,
the data from this FY 2007 cost report would appropriately be matched
to IRF discharges occurring from October 1, 2007 through June 30, 2008
(i.e., during FY 2008) because these claims would fall during the
period of time covered by the IRF's ``FY 2007'' cost report year. In
the case of FY 2008 claims that would appropriately match to an IRF's
FY 2008 cost report year, we used the FY 2008 cost report data when
available. In instances in which the matching FY 2008 cost report data
were not available, we used the most recent available data, which in
these cases was the FY 2007 cost report data.
For this final rule, as many commenters suggested, we are updating
the rural, LIP, and teaching status adjustment factors using more
recent data (FY 2006, FY 2007, and FY 2008 claims data and the
corresponding year's cost report data or, if unavailable, the most
recent available cost report data). We note, however, that we only have
about 20 percent of the IRF cost reports from FY 2008 available for
analysis at this time, so although we did use the FY 2008 cost report
data that we had available, in some cases we had to use a prior year's
cost report data to match to some of the FY 2008 IRF claims, as
discussed above. Although the adjustment factors for the rural and LIP
adjustments that we estimate in this final rule using updated data
(18.4 percent and 0.4613, respectively) do not differ substantially
from the adjustment factors that we calculated using the methods set
forth in the proposed rule (18.27 percent and 0.4372, respectively),
the teaching status adjustment factor that we calculate in this final
rule using updated data (0.6876) is significantly lower than the
teaching status adjustment factor that we calculated in the proposed
rule (1.0494). This is due to the relatively large year-to-year
fluctuations in the teaching status adjustment factor noted in the
proposed rule (74 FR 21052 at 21061).
We believe that it is necessary to update these adjustment factors
at this time because the adjustment factors that are being used
currently to calculate the rural, LIP, and teaching status adjustments
are based on FY 2003 data (as finalized in the FY 2006 IRF PPS final
rule (70 FR 47880, 47928 through 47934)), and the FY 2003 data do not
reflect recent changes in IRF patient populations resulting from the 60
percent rule and medical review activities.
The current adjustment factors for the rural, LIP, and teaching
status adjustments in the FY 2006 IRF PPS final rule (70 FR 47928
through 47934) are based on regression analysis by the RAND Corporation
(RAND) using FY 2003 IRF claims and cost report data. In the FY 2010
IRF PPS proposed rule (74 FR 21052, 21059 through 21062), we proposed
to use the same methodology RAND used in computing these
[[Page 39774]]
adjustment factors. However, we proposed to compute the adjustment
factors using three consecutive years of claims data and the
corresponding year's cost report data or, when not available, the most
recent available cost report data and to average the calculated
adjustment factors for all three years to develop the proposed rural,
LIP, and teaching status adjustment factors for FY 2010. As discussed
in the FY 2010 IRF PPS proposed rule (74 FR 21052, 21059 through
21061), we received a comment on the FY 2009 IRF PPS proposed rule (73
FR 22674) suggesting that we consider a three-year moving average
approach because it would provide a more stable adjustment factor,
enabling IRFs to project their future Medicare payments more
accurately. We analyzed the suggestion and agree that a three year
average of the adjustment factors would promote more stability in the
adjustment factors over time, which we believe will benefit IRFs by
ensuring reduced variation from year to year and facilitating IRFs'
long-term budgetary planning processes.
We received 12 comments on the proposed updates to the rural, LIP,
and teaching status adjustment factors for FY 2010, which are
summarized below.
Comment: The commenters overwhelmingly supported the proposed
three-year moving average approach to updating the rural, LIP, and
teaching status adjustment factors, saying that this approach makes
payments to IRFs more stable and predictable over time. The commenters
further requested that CMS continue to use this methodology to update
these facility-level adjustment factors annually in the future to
ensure that they continue to reflect the costs of care in IRFs.
Response: We agree that using the three-year moving average
approach will provide greater stability and predictability of Medicare
payments for IRFs, and will finalize this methodology to update the
facility-level adjustment factors for FY 2010 and future years.
Comment: One commenter expressed concerns about the proposed
decrease in the rural adjustment factor for FY 2010 and asked us to
explain what cost factors we believe may have caused the estimated
decrease in the rural adjustment factor.
Response: We believe that it is important to adjust payments for
rural IRFs to reflect the higher costs that IRFs in rural areas incur
for providing services in these areas. However, the results of our
analysis using the most recent available data and the three-year moving
average approach indicate that a rural adjustment factor of 18.4
percent more accurately reflects the current costs of providing IRF
services in rural areas.
Further, we believe that the estimated decrease in the rural
adjustment factor for FY 2010 (from 21.3 percent to 18.4 percent) is,
in part, the result of improvements we made to the IRF classification
system in the FY 2006 and FY 2007 IRF PPS final rules (70 FR 47880,
47886 through 47904 and 71 FR 48354, 48373 through 48374). Those
improvements were designed to account more appropriately for the
variation in costs among different types of IRF patients. To the extent
that some of the differences in costs that we previously observed
between rural and urban IRFs were the result of differences in patient
populations, better accounting for the variations in costs among
patients may have reduced the need to account for differences in costs
between rural and urban IRFs.
Comment: The Medicare Payment Advisory Commission (MedPAC)
suggested that CMS conduct research on the IRF teaching status
adjustment to determine why the teaching status adjustment factor
appears to vary so much from year to year, and to evaluate the accuracy
and reliability of the adjustment. In the meantime, MedPAC suggested
that CMS consider alternatives to the 3-year moving average approach,
such as maintaining the IRF teaching adjustment at its FY 2009 level,
capping the adjustment at the level currently in place for IPPS
hospitals or inpatient psychiatric facilities (IPFs), or capping the
adjustment at a level equal to MedPAC's estimate of the empirically
justified IME adjustment for IPPS hospitals. MedPAC notes that the
purpose of these alternatives would be to either maintain the teaching
status adjustment at its current level or reduce the adjustment.
Response: As we reported in the FY 2010 IRF PPS proposed rule (74
FR 21052 at 21061), we estimate that the teaching status adjustment
factors would be 1.5155, 0.6732, and 1.0451 using FY 2005, FY 2006, and
FY 2007 data, respectively. In addition, for this final rule, we
estimate that the teaching status adjustment factor would be 0.4045
using FY 2008 data. We are still analyzing the reasons for such large
fluctuations in the teaching status adjustment factors from year to
year. However, we believe that it may be due, in part, to relatively
large fluctuations in the teaching variable (number of interns and
residents divided by the average daily census) that we observe in the
data between FY 2005 and FY 2008. On average, the teaching variable for
all teaching IRFs was 0.1164, 0.1207, 0.1160, and 0.1295 in FYs 2005,
2006, 2007, and 2008, respectively. We believe that this variation may
reflect provider responses to the implementation of the IRF teaching
status adjustment in FY 2006, and that we may see less variation over
time as IRFs adjust to this new payment adjustment.
However, to mitigate the impact on payments of annual fluctuations
in the facility-level adjustment factors, we have proposed to use and,
by this rule, adopt a three-year moving average approach instead of
using only one year's worth of data to calculate the rural, LIP, and
teaching status adjustment factors for FY 2010. Using the 3-year moving
average approach and updated IRF claims data from FYs 2006 through
2008, we calculate a teaching status adjustment factor for this final
rule of 0.6876, which is less than the factor 0.9012 that was applied
to IRF PPS payments from FY 2006 through FY 2009. Since the teaching
status adjustment factor for this final rule is lower than the current
factor, we do not believe that it is necessary to consider the
alternative ``capping'' methodologies suggested by MedPAC at this time.
However, we will continue to monitor the data and work with MedPAC to
analyze the reasons for the year-to-year fluctuations.
Comment: Several commenters requested that we use FY 2008 IRF
claims and cost report data to update the facility-level adjustment
factors for FY 2010.
Response: We appreciate the commenters' suggestions for updating
the data used in the analysis of the IRF facility-level adjustment
factors for FY 2010, and we agree that we should continue to use the
most recent available data for these analyses. However, only about 20
percent of the FY 2008 IRF cost reports are available for analysis at
this time. Thus, for this final rule, we have continued to use the most
recent available data, which are the FY 2006, FY 2007, and FY 2008 IRF
claims data and the corresponding year's cost report data or, if
unavailable, the most recent available cost report data.
Final Decision: After carefully considering all of the comments
that we received on the proposed updates to the rural, LIP, and
teaching status adjustment factors for FY 2010, including the
overwhelming support for the proposed use of a three-year moving
average approach to calculating these adjustment factors, we are
finalizing the following updates to the rural, LIP, and teaching status
adjustment factors for FY 2010. Note that these updated
[[Page 39775]]
adjustment factors were calculated using the same methodology RAND used
in calculating the current adjustment factors but using updated FY
2006, FY 2007, and 2008 IRF claims data and the corresponding year's
cost report data or, if unavailable, the most recent available cost
report data. IRF PPS payments to IRFs in rural areas will be increased
by 18.4 percent for FY 2010. IRF PPS payments will be adjusted for FY
2010 to account for the percentage of low-income patients that an IRF
treats using the updated LIP adjustment formula of (1 +
disproportionate share hospital (DSH) patient percentage) raised to the
power of (0.4613), where the DSH patient percentage for each IRF =
[GRAPHIC] [TIFF OMITTED] TR07AU09.000
Finally, IRF PPS payments to eligible IRFs that qualify for the
teaching status adjustment will be adjusted by the following updated
formula for FY 2010: (1 + full-time equivalent (FTE) residents/average
daily census) raised to the power of (0.6876). Note that the rural,
LIP, and teaching status adjustment factors for FY 2010 differ from
those proposed in the FY 2010 IRF PPS proposed rule (74 FR 21052, 21060
through 21061) due to the use of updated data in this final rule.
To calculate the updates to the rural, LIP, and teaching status
adjustment factors for FY 2010, we used the following steps:
[Steps 1 and 2 are performed independently for each of three years
of IRF claims data: FY 2006, FY 2007, and FY 2008]
Step 1. Calculate the average cost per case for each IRF in the IRF
claims data using the corresponding year's cost report data or, if
unavailable, the most recent available cost report data, as described
above.
Step 2. Use logarithmic regression analysis on average cost per
case to compute the coefficients for the rural, LIP, and teaching
status adjustments.
Step 3. Calculate a simple mean for each of the coefficients across
the three years of data using logarithms for the LIP and teaching
status adjustment coefficients (because they are continuous variables)
but not using logarithms for the rural adjustment coefficient (because
the rural variable is 1 if the facility is rural and zero otherwise).
To compute the LIP and teaching status adjustment factors, we convert
these factors back out of the logarithmic form.
B. Budget Neutrality Methodology for the Updates to the IRF Facility-
Level Adjustment Factors
Consistent with the way that we implemented changes to the IRF
facility-level adjustment factors (the rural, LIP, and teaching status
adjustment factors) in the FY 2006 IRF PPS final rule (70 FR 47880 and
70 FR 57166), which was the only year in which we updated these
adjustment factors, we are updating the rural, LIP, and teaching status
adjustment factors for FY 2010 in such a way that total estimated
aggregate payments to IRFs for FY 2010 will be the same with or without
the updates (that is, in a budget neutral manner) by applying budget
neutrality factors for each of these three changes to the standard
payment amount. To calculate the budget neutrality factors used to
update the rural, LIP, and teaching status adjustment factors, we used
the following steps:
Step 1. Using the most recent available data (currently FY 2008),
calculate the estimated total amount of IRF PPS payments that would be
made in FY 2010 (without applying the update to the rural, LIP, or
teaching status adjustment factors).
Step 2. Calculate the estimated total amount of IRF PPS payments
that would be made in FY 2010 if the update to the rural adjustment
factor were applied.
Step 3. Divide the amount calculated in step 1 by the amount
calculated in step 2 to determine the budget neutrality factor (1.0023)
that would maintain the same total estimated aggregate payments in FY
2010 with and without the update to the rural adjustment factor.
Step 4. Calculate the estimated total amount of IRF PPS payments
that would be made in FY 2010 if the update to the LIP adjustment
factor were applied.
Step 5. Divide the amount calculated in step 1 by the amount
calculated in step 4 to determine the budget neutrality factor (1.0192)
that would maintain the same total estimated aggregate payments in FY
2010 with and without the update to the LIP adjustment factor.
Step 6. Calculate the estimated total amount of IRF PPS payments
that would be made in FY 2010 if the update to the teaching status
adjustment factor were applied.
Step 7. Divide the amount calculated in step 1 by the amount
calculated in step 6 to determine the budget neutrality factor (1.0037)
that would maintain the same total estimated aggregate payments in FY
2010 with and without the update to the teaching status adjustment
factor.
Step 8. Apply the budget neutrality factors for the updates to the
rural, LIP, and teaching status adjustment factors to the FY 2009 IRF
PPS standard payment amount after the application of the budget
neutrality factors for the wage adjustment and the CMG relative
weights.
The budget neutrality factors for the updates to the rural, LIP,
and teaching status adjustment factors in this final rule differ from
those described in the proposed rule (74 FR 21052, 21061 through 21062)
due to the use of updated data for the analysis in this final rule.
In section VI.C of this final rule, we discuss the methodology for
calculating the final standard payment conversion factor for FY 2010.
VI. FY 2010 IRF PPS Federal Prospective Payment Rates
A. Market Basket Increase Factor and Labor-Related Share for FY 2010
Section 1886(j)(3)(C) of the Act requires the Secretary to
establish an increase factor that reflects changes over time in the
prices of an appropriate mix of goods and services included in the
covered IRF services, which is referred to as a market basket index.
According to section 1886(j)(3)(A)(i) of the Act, the increase factor
shall be used to update the IRF Federal prospective payment rates for
each FY. Section 115 of the MMSEA amended section 1886(j)(3)(C) of the
Act to apply a zero percent increase factor for FYs 2008 and 2009,
effective for IRF discharges occurring on or after April 1, 2008. In
the absence of any such amendment for FY 2010, we are updating IRF PPS
payments by a market basket increase factor based upon the most current
data available in accordance with section 1886(j)(3)(A)(i) of the Act.
Beginning with the FY 2006 IRF PPS final rule (70 FR 47908 through
47917), the market basket index used to update IRF payments is a 2002-
based market basket reflecting the operating and
[[Page 39776]]
capital cost structures for freestanding IRFs, freestanding inpatient
psychiatric facilities (IPFs), and long-term care hospitals (LTCHs)
(hereafter referred to as the rehabilitation, psychiatric, and long-
term care (RPL) market basket).
For this final rule, we have used the same methodology described in
the FY 2006 IRF PPS Final Rule (70 FR 47908 through 47917) to compute
the FY 2010 market basket increase factor and labor-related share.
Using this method and the IHS Global Insight, Inc. forecast for the
second quarter of 2009 of the 2002-based RPL market basket, the FY 2010
IRF market basket increase factor is 2.5 percent. IHS Global Insight is
an economic and financial forecasting firm that contracts with CMS to
forecast the components of providers' market baskets.
Also, using the methodology described in the FY 2006 IRF PPS final
rule (70 FR 47880, 47908 through 47917), we are updating the IRF labor-
related share for FY 2010. Using this method and the IHS Global
Insight, Inc. forecast for the second quarter of 2009 of the 2002-based
RPL market basket, the IRF labor-related share for FY 2010 is the sum
of the FY 2010 relative importance of each labor-related cost category.
This figure reflects the different rates of price change for these cost
categories between the base year (FY 2002) and FY 2010. Consistent with
our proposal to update the labor-related share with the most recent
available data, the labor-related share for this final rule reflects
IHS Global Insight's second quarter 2009 forecast of the 2002-based RPL
market basket. As shown in Table 2, the FY 2010 labor-related share is
75.779 percent.
Table 2--FY 2010 IRF RPL Labor-Related Share Relative Importance
------------------------------------------------------------------------
FY 2010 IRF
labor-
related
Cost category share
relative
importance
------------------------------------------------------------------------
Wages and salaries......................................... 52.892
Employee benefits.......................................... 13.949
Professional fees.......................................... 2.873
All other labor intensive services......................... 2.127
------------
Subtotal............................................... 71.841
Labor-related share of capital costs (.46)................. 3.938
------------
Total.................................................. 75.779
------------------------------------------------------------------------
Source: IHS GLOBAL INSIGHT, INC, 2nd QTR, 2009; @USMACRO/CONTROL0609
@CISSIM/TL0509.SIM Historical Data through 1st QTR, 2009.
We received 10 comments on the proposed updates to the IRF market
basket increase factor and labor-related share for FY 2010, which are
summarized below.
Comment: One commenter supported the creation of a stand-alone IRF
market basket based on both freestanding and hospital-based cost report
data. The commenter offered the following suggestions that CMS could
pursue in order to account for the differences in costs between the two
facility types.
Those suggestions included:
1. To survey a random sample of facilities to assess the presence
of the array of rehabilitation services that may be available through
the freestanding IRF as compared to a hospital-based IRF.
2. To conduct detailed interviews of the Chief Financial Officers
(CFOs) of freestanding versus hospital based units to understand the
differences in the ways IRF costs are accounted for in cost reports.
Response: We appreciate the commenter's response concerning the
stand-alone IRF market basket and the suggestions that were provided.
CMS will take the suggestions into consideration as we continue to
research the differences between hospital-based and freestanding
facilities.
Comment: Several commenters noted that the use of 2002 data is
inappropriate because of major changes to IRF case mix and patient
severity and requested CMS update the cost weights of the existing RPL
market basket to a more recent base year.
Response: We recognize the commenters' concerns regarding the
continued use of 2002 data in the RPL market basket. We have focused
our recent efforts on comparing and contrasting the costs and cost
structures of freestanding and hospital-based IRFs, including the
effects of changes to case mix and patient severity over the last
several years. We will consider the suggestions that we received during
the comment period to better understand those differences (and further
investigate the appropriateness of creating a stand-alone IRF market
basket), as well as examine the appropriateness of rebasing and
revising the RPL market basket.
Comment: One commenter noted that the data used to calculate the
RPL market basket are obtained from freestanding IRFs, freestanding
IPFs, and LTCHs. The commenter expressed the concern that each facility
type requires different resources and thus combining the three types of
facilities distorts the cost structures of IRFs. This commenter also
suggested incorporating the most recent available data into the market
basket.
Response: CMS recognizes the existence of differences in cost
structures across freestanding IPFs, freestanding IRFs, and LTCHs.
However, pending further research into the viability of creating a
stand-alone IRF market basket, we feel that it is appropriate to
continue to use the current 2002-based RPL market basket to update IRF
payments. We will examine the appropriateness of rebasing and revising
the RPL market basket for the future.
Comment: Several commenters offered that one reason for the
difference between freestanding and hospital-based IRFs cost structures
is that most hospital-based units are smaller than freestanding IRFs.
For example, one commenter indicated that hospital-based IRFs have
nearly two-thirds fewer discharges than freestanding IRFs. Thus, the
commenters claimed that hospital-based IRFs may be unable to achieve
the same level of economies of scale as freestanding IRFs can.
Response: We have noted that cost differences between hospital-
based and freestanding IRFs may be due to the volume of care that
hospital-based facilities provide relative to freestanding facilities.
In an attempt to control for differences in the volume of services, we
have compared costs per discharge and costs per day between the two
facility types and continue to find differences in their overall cost
levels. Notably, CMS feels that, all other things held constant,
differing volumes may not necessarily explain differing cost structures
as the cost weights reflect the relative expense of one category to
another within a facility. We will continue to evaluate our findings
related to these metrics with new data as it becomes available.
Comment: One commenter mentioned that one contributing cause of the
difference in cost structures between freestanding and hospital-based
IRFs is the issue of costs being allocated down from the IPPS hospital
to the hospital-based IRF unit.
Response: We share the commenter's concern that overhead costs from
the host hospital may be skewing the hospital-based unit's costs and
cost structure. One of the main reasons why CMS has historically relied
on Medicare cost report data from freestanding facilities to construct
the market baskets is our concern over the distribution of the host
hospital's overhead costs to the sub-provider units. We will continue
to investigate the allocation of overhead
[[Page 39777]]
costs from the host hospital to the hospital-based IRF unit.
Comment: One commenter acknowledged that seeking outside input
regarding differences in cost structures between hospital-based and
freestanding IRFs is appropriate. However, the commenter urged CMS to
proceed with caution as it may be difficult for CMS to confir