Medicare Program; Inpatient Prospective Payment Systems; 0.2 Percent Reduction, 75107-75117 [2015-30486]
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[FR Doc. 2015–30357 Filed 11–30–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–1658–NC]
RIN 0938–ZB23
Medicare Program; Inpatient
Prospective Payment Systems; 0.2
Percent Reduction
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice with comment period.
AGENCY:
In accordance with the
Court’s October 6, 2015 order in Shands
Jacksonville Medical Center, Inc., et al.
v. Burwell, No. 14–263 (D.D.C.) and
consolidated cases that challenge the 0.2
percent reduction in inpatient
prospective payment systems (IPPS)
rates to account for the estimated $220
million in additional FY 2014
expenditures resulting from the 2midnight policy, this notice discusses
the basis for the 0.2 percent reduction
and its underlying assumptions and
invites comments on the same in order
to facilitate our further consideration of
the FY 2014 reduction. We will consider
and respond to the comments received
in response to this notice, and to
comments already received on this issue
in a final notice to be published by
March 18, 2016.
DATES: Comment date: To be assured
consideration, comments must be
received at one of the addresses
provided below, no later than 5 p.m.
e.s.t. on February 2, 2016.
ADDRESSES: In commenting, refer to file
code CMS–1658–NC. Because of staff
and resource limitations, we cannot
accept comments by facsimile (FAX)
transmission.
You may submit comments in one of
four ways (please choose only one of the
ways listed):
1. Electronically. You may submit
electronic comments on this notice to
https://www.regulations.gov. Follow the
‘‘Submit a comment’’ instructions.
2. By regular mail. You may mail
written comments to the following
address ONLY: Centers for Medicare &
SUMMARY:
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75107
Medicaid Services, Department of
Health and Human Services, Attention:
CMS–1658–NC, P.O. Box 8013,
Baltimore, MD 21244–8013.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments to the
following address ONLY: Centers for
Medicare & Medicaid Services,
Department of Health and Human
Services, Attention: CMS–1658–NC,
Mail Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
4. By hand or courier. Alternatively,
you may deliver (by hand or courier)
your written comments ONLY to the
following addresses:
a. For delivery in Washington, DC—
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, Room 445–G, Hubert
H. Humphrey Building, 200
Independence Avenue SW.,
Washington, DC 20201.
(Because access to the interior of the
Hubert H. Humphrey Building is not
readily available to persons without
Federal government identification,
commenters are encouraged to leave
their comments in the CMS drop slots
located in the main lobby of the
building. A stamp-in clock is available
for persons wishing to retain a proof of
filing by stamping in and retaining an
extra copy of the comments being filed.)
b. For delivery in Baltimore, MD—
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
If you intend to deliver your
comments to the Baltimore address, call
telephone number (410) 786–9994 in
advance to schedule your arrival with
one of our staff members.
Comments erroneously mailed to the
addresses indicated as appropriate for
hand or courier delivery may be delayed
and received after the comment period.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: IngJye Cheng, (410) 786–2260 or Don
Thompson, 410–786–6504.
SUPPLEMENTARY INFORMATION: Inspection
of Public Comments: All comments
received before the close of the
comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following Web
site as soon as possible after they have
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been received: https://
www.regulations.gov. Follow the search
instructions on that Web site to view
public comments.
Comments received timely will also
be available for public inspection as
they are received, generally beginning
approximately 3 weeks after publication
of a document, at the headquarters of
the Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday
through Friday of each week from 8:30
a.m. to 4 p.m. e.s.t. To schedule an
appointment to view public comments,
phone 1–800–743–3951.
I. Background
In the final rule titled ‘‘Medicare
Program; Hospital Inpatient Prospective
Payment Systems for the Acute Care
Hospitals and the Long-Term Care
Hospital Prospective Payment System
and Final Fiscal Year 2014 Rates;
Quality Reporting Requirements for
Specific Providers; Hospital Conditions
of Participation; Payment Policies
Related to Patient Status’’ (hereinafter
referred to as the FY 2014 IPPS/LTCH
PPS final rule), we adopted the 2midnight policy effective October 1,
2013 (78 FR 50906 through 50954).
Under the 2-midnight policy, an
inpatient admission is generally
appropriate for Medicare Part A
payment if the physician (or other
qualified practitioner) admits the
patient as an inpatient based upon the
expectation that the patient will need
hospital care that crosses at least 2
midnights. In assessing the expected
duration of necessary care, the
physician (or other practitioner) may
take into account outpatient hospital
care received prior to inpatient
admission. If the patient is expected to
need less than 2 midnights of care in the
hospital, the services furnished should
generally be billed as outpatient
services. Our actuaries estimated that
the 2-midnight policy would increase
expenditures by approximately $220
million in FY 2014 due to an expected
net increase in inpatient encounters. We
used our authority under section
1886(d)(5)(I)(i) of the Act to make a
reduction of 0.2 percent to the
standardized amount, the Puerto Rico
standardized amount, and the hospitalspecific payment rate, and we used our
authority under section 1886(g) of the
Act to make a reduction of 0.2 percent
to the national capital Federal rate and
the Puerto Rico-specific capital rate, in
order to offset this estimated $220
million in additional IPPS expenditures
in FY 2014. (In addition to an operating
IPPS payment for each discharge,
hospitals also receive a capital IPPS
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payment for each discharge so a net
increase in the number of inpatient
encounters also results in increased
expenditures under the capital IPPS.)
II. Supplemental Notice Requesting
Comments on the FY 2014 IPPS Rule
A. Overview
As noted in section I. of this notice
with comment period, we estimated
based on an actuarial model that the 2midnight policy would increase IPPS
expenditures by approximately $220
million in FY 2014 due to an expected
net increase in inpatient encounters, as
described in greater detail in an August
19, 2013 memorandum. (See Appendix
A of this notice.)
Section II.B. of this notice with
comment period provides additional
details on the calculation of this
estimate (that is, what we did) and
section II.C. of this notice with comment
period discusses the actuaries’
assumptions, including why those
assumptions were reasonable. We
collectively refer to the calculations and
assumptions as the actuarial ‘‘model’’
for estimating the financial impact of
the policy change. Section II.D. of this
notice with comment period discusses
the status of an analysis currently being
conducted by our actuaries of the claims
experience since the implementation of
the 2-midnight policy. We seek
comment on all aspects of the model
used by our actuaries, including but not
limited to those for which we
specifically request comment. We seek
comment on, and will consider
comments on, all aspects of the 0.2
percent reduction.
B. Calculation of the Impact of the
2-Midnight Policy
The task of modeling the impact of
the 2-midnight policy on hospital
payments begins with a recognition that
some cases that were previously
outpatient cases will become inpatient
cases and vice versa. Therefore, our
actuaries were required to develop a
model that determined the net effect of
the number of cases that would move in
each direction.
In estimating the number of
outpatient cases that would shift to the
inpatient setting, we analyzed calendar
year (CY) 2011 claims that included
spending for observation care or a major
procedure. For the purposes of the ¥0.2
percent estimate, CMS physicians
defined observation care as Outpatient
Prospective Payment System (OPPS)
claims containing Healthcare Common
Procedure Coding System (HCPCS) code
‘‘G0378’’, Hospital observation service,
per hour, or HCPCS code ‘‘G0379’’
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Direct admission of patient for hospital
observation care. We used the difference
between the first date of service for the
HCPCS code (generally the first date
that the service represented by that code
was provided to the patient) and the
‘‘claim through’’ date (generally the last
date any service on the claim was
provided to the patient) to determine
the length of the observation care. In
this manner, we identified
approximately 350,000 observation care
stays of 2 midnights or more using the
CY 2011 claims.
A list of the Ambulatory Payment
Classifications (APCs) containing the
major procedures used in the
determination of the ¥0.2 percent
estimate can be found in Appendix B of
this notice with comment period. As
with observation care, the difference
between the first date of service for the
HCPCS code and the claim through date
was used to determine the length of the
major procedure. We identified
approximately 50,000 claims containing
major procedures with stays lasting 2
midnights or more using the CY 2011
claims.
Combining the observation care and
the major procedures resulted in
approximately 400,000 claims for
services of 2 midnights or more from the
CY 2011 claims data.
For additional details on the
identification of the outpatient claims,
see Appendix C of this notice with
comment period.
In estimating the number of inpatient
stays that would shift to the outpatient
setting, FY 2011 inpatient claims
containing a surgical Medicare Severity
Diagnosis Related Group (MS–DRG)
were analyzed. The number of these
stays that spanned less than 2
midnights, based on the length of stay,
was approximately 360,000. FY 2009
and FY 2010 data were also analyzed
and the results were consistent with the
FY 2011 results.
For additional details on the
identification of the inpatient claims,
see Appendix D of this notice with
comment period.
Our actuaries also assumed that
payment under the OPPS would be 30
percent of the payment under the IPPS
for encounters shifting between the two
systems, and that the beneficiary is
responsible for 20 percent of the Part B
cost.
The number of short stay discharges
(for this purpose, same day discharges
and discharges crossing one or two
midnights) represented about 28 percent
of total discharges in FY 2011, and
approximately 17 percent of total
spending for the total discharges. The
assumed net increase of 40,000
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inpatient discharges (= 400,000 OPPS to
IPPS—360,000 IPPS to OPPS)
represented an increase of 1.2 percent in
the number of short stay discharges.
Taking 1.2 percent of 17 percent of total
spending results in the estimate at the
time of the FY 2014 IPPS/LTCH PPS
rulemaking that the 2-midnight policy
would result in an additional $290
million in inpatient expenditures, as
shown for FY 2014 in the table ‘‘Impact
on Medicare Expenditures’’ found in the
memorandum in Appendix A of this
notice. The estimates for the additional
inpatient expenditures for FYs 2015
through 2018 can also be found in the
table (for example, $320 million for FY
2015).
For the outpatient expenditure
estimate, taking 30 percent (based on
the assumption that payment under the
OPPS would be 30 percent of the
payment under the IPPS) of 80 percent
(to account for the assumed 20 percent
beneficiary responsibility) of the $290
million inpatient estimate results in
approximately $70 million less
outpatient expenditures. The estimates
for the reduction in outpatient
expenditures for FYs 2015 through 2018
can also be found in the table (For
example, $80 million for FY 2015.)
The estimated $290 million increase
in inpatient expenditures less the
estimated $70 million decrease in
outpatient expenditures yields the
estimated net impact by our actuaries at
the time of the FY 2014 IPPS/LTCH PPS
rulemaking of an additional $220
million in expenditures in FY 2014 as
a result of the 2-midnight policy. The
estimated additional expenditures for
FYs 2015 through 2018 can be similarly
calculated.
Using the information contained in
this section and the appendices to this
notice, interested members of the public
should be able to calculate the estimate
by our actuaries of an additional $220
million in expenditures in FY 2014 as
a result of the 2-midnight policy. (For
interested members of the public who
wish to perform this calculation, we
highlight the discussion in Appendix D
regarding the number of inpatient cases
identified in the MedPAR data and the
Integrated Data Repository.)
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C. Discussion of the Assumptions Made
in the Calculation of the Impact of the
2-Midnight Policy
As our actuaries stated in the August
2013 memorandum, the estimates
depend critically on the assumed
utilization changes in the inpatient and
outpatient hospital settings. We discuss
the assumptions underlying the
estimates further in this section.
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1. Estimated Outpatient Cases That
Would Shift to the Inpatient Setting
As indicated previously, in estimating
the number of outpatient cases that
would shift to the inpatient setting, CY
2011 claims that included spending for
observation care or a major procedure
were analyzed. This was done in order
to remove claims with diagnostic
services or minor procedures that would
be less likely to trigger an encounter in
which there was a continuous stay. (See
the discussion in Appendix C of this
notice with comment period.)
For the purpose of the ¥0.2 percent
estimate, observation care was defined
as OPPS claims containing HCPCS
‘‘G0378,’’ Hospital observation service,
per hour, or ‘‘G0379’’ Direct admission
of patient for hospital observation care.
At the time the ¥0.2 percent estimate
was being developed, we were also
examining establishing comprehensive
APCs under the OPPS (for a summary of
the results of this examination see the
CY 2014 OPPS proposed rule (78 FR
43540)). One of the claims analyses that
we developed for this purpose included
service counts of G0378 and G0379 and
significant procedures. Since this
analysis included the universe of
services of interest for the 2-midnight
policy at that time, it was well-suited for
use in the development of the ¥0.2
percent estimate as well. For a
discussion of the data specifications for
this claims analysis, and how it was
subset for the 2-midnight analysis, see
Appendix C of this notice with
comment period.
However, in retrospect, using HCPCS
G0378 and G0379 may have been an
overly conservative definition of
observation services, because not every
use of observation services would be
captured by the G-codes. As indicated
in the Medicare Claims Processing
Manual,1 hospitals are required to
report observation charges under the
revenue center code ‘‘0760’’, Treatment
or observation room—general
classification, or ‘‘0762’’ Treatment or
observation room—observation room
regardless of whether or not the G-codes
are billed.
We also note that the Office of the
Inspector General (OIG) used this
revenue center code definition of
observation services in its report
‘‘Hospitals’ Use of Observation Stays
and Short Inpatient Stays 2 (OEI–02–12–
00040).
1 See section 290.2.1 in Chapter 4 of the Medicare
Claims Processing Manual available at https://
www.cms.gov/Regulations-and-Guidance/
Guidance/Manuals/downloads/clm104c04.pdf)
2 Available at https://oig.hhs.gov/oei/reports/oei02-12-00040.pdf.
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If we had defined observation services
using revenue center codes 0760 and
0762 instead of HCPCS codes G0378
and G0379, we would have identified
approximately 400,000 claims for
observation services spanning 2
midnights or more (instead of 350,000)
and we would have estimated
approximately 450,000 cases shifting
from the outpatient to the inpatient
setting (400,000 claims for observation
stays spanning more than 2 midnights
and approximately 50,000 claims for
major procedures) instead of the
400,000 cases used in the estimate. We
seek comment on whether it would be
more appropriate to define observation
services using revenue center codes
0760 and 0762 rather than HCPCS codes
G0378 and G0379.
Another consequence of the use of the
claims analyses that we developed for
the purpose of the comprehensive APCs
involves the approach used to
determine whether observation stays
spanned 2 midnights or more. In
general, in the claims analysis for
comprehensive APC development, we
examined the difference between the
date of service for the primary HCPCS
code on the claim and the claim through
date. For the observation services in this
analysis, we used the difference
between first date of service for the
observation service and the claim
through date to determine the length of
the observation case. However, in
retrospect, as with the definition of
observation services, this may have been
an overly conservative approach to
determining the length of the
observation case. Under the 2-midnight
policy, for purposes of determining
whether the 2 midnight benchmark was
met and, therefore, whether inpatient
admission was generally appropriate,
the expected duration of care includes
the time the beneficiary spent receiving
outpatient services within the hospital.
This includes services such as
observation services, treatments in the
emergency department, and procedures
provided in the operating room or other
treatment area. It is not just the time
spent receiving observation services. As
such, it may have been more
appropriate to have used the ‘‘claim
from’’ date (in general the date that the
beneficiary entered the hospital), rather
than the first date that observation
services were provided in order to
determine when claims containing
observation services spanned 2
midnights or more. If we had used such
an approach when developing the
original estimate, instead of
approximately 350,000 claims with
observation services spanning 2
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midnights or more, the estimate would
have been approximately 430,000
claims under the HCPCS code G0378/
G0370 definition of observation services
and approximately 520,000 under the
revenue center code 0760/0762
definition of observation services. When
combined with our estimate of major
procedures, we would have estimated as
many as 570,000 cases shifting from the
outpatient to the inpatient setting under
this approach instead of the 400,000
cases used in the estimate. We seek
comment on whether it would be more
appropriate to have used the claim from
date rather than the first date that
observation services were provided in
order to determine when claims
containing observation services spanned
2 midnights or more.
2. Estimated Inpatient Cases That
Would Shift to the Outpatient Setting
We believed some proportion of the
inpatient cases under 2 midnights in the
historical data would remain inpatient
because we believed that behavioral
changes by hospitals and admitting
practitioners would mitigate some of the
impact of cases shifting between the
inpatient hospital setting and the
outpatient hospital setting. The question
was how to reasonably estimate what
that proportion would be for purposes
of modelling the impact of the 2midnight policy. We believe that a
model distinguishing between medical
and surgical cases is a reasonable
approach to use in determining what
proportion of inpatient cases would
remain in the inpatient setting and what
proportion would shift to the outpatient
setting.
Specifically, in estimating the number
of inpatient stays that would shift to the
outpatient setting, FY 2011 inpatient
claims containing a surgical MS–DRG
were analyzed. Our actuaries assumed
that those spanning less than 2
midnights (other than those stays that
were cut short by a death or transfer)
would shift from the inpatient setting to
the outpatient setting. Stays that were
cut short by a death or transfer were
excluded because under the 2-midnight
policy those cases would generally be
considered to be appropriately treated
on an inpatient basis. (For a discussion
of the data specifications for the
inpatient claims analysis, see Appendix
D of this notice.)
Claims containing medical MS–DRGs
were excluded because, as stated in the
August 2013 memorandum, ‘‘it was
assumed that these cases would be
unaffected by the policy change.’’ Our
actuaries excluded medical MS–DRGs
when developing the ¥0.2 percent
estimate because they believed that due
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to behavioral changes by hospitals and
admitting practitioners most inpatient
medical encounters spanning less than
2 midnights before the current 2midnight policy was implemented
might be reasonably expected to extend
past 2 midnights after its
implementation and would thus still be
considered inpatient. They believed that
the clinical assessments and protocols
used by physicians to develop an
expected length of stay for medical
cases were, in general, more variable
and less defined than those used to
develop an expected length of stay for
surgical cases.
Evidence of this medical/surgical
dichotomy is seen in proprietary
utilization review tools such as the
Milliman Care Guidelines, which are
guidelines based originally on actuarial
data, and InterQual, which are clinically
oriented guidelines. Both tools reflect
the same types of distinctions between
medical and surgical cases that we
assumed based on CMS medical staff’s
clinical judgment. Although all
guidelines, and all surgeons, advise
patients that individual patients vary in
their post-operative courses, there are
predictable post-operative courses that
are based on such factors as whether or
not the abdominal cavity or the pleural
cavity are entered, the expected time for
recovery from anesthesia, the expected
time to resume urinary function, the
expected time to resume bowel
function, the expected time to regain
mobility, and the typical period for
common post-operative interventions.
These are by no means absolute but are
fairly well-defined, as evidenced by the
surgeon’s ability to generally inform the
patient, within a day or so, how long the
patient probably can expect to remain in
the hospital if treatment goes well. Part
of this decreased variance is due to the
fact that the reason for admission, a
specific surgical procedure, is welldefined.
Conversely, for medical admissions a
single diagnosis typically covers a much
broader spectrum of possibilities.
Pneumonia may have different
etiologies, with vastly different expected
lengths of stay. A stroke may be minor,
allowing a brief diagnostic workup to be
followed by outpatient rehabilitation, or
catastrophic, triggering a prolonged stay
before stabilization and discharge.
Chronic obstructive pulmonary disease
(COPD) and congestive heart failure
(CHF) may respond rapidly to
medication adjustments or may result in
Intense Care Unit (ICU) stays. Unlike the
surgical procedure, the medical
diagnosis does not imply a reasonably
consistent set of activities. In fact,
typical medical protocols are highly
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branched, with the initial portion of
hospital care typically focused on
diagnostics that serve to differentiate
patient subsets that define treatments
and simultaneously suggest different
hospital courses. The increased
variability in the medical protocols is
influenced by the fact that, for planned
surgical admissions, more of the
branching takes place in the process of
selecting a specific surgical intervention
before the patient is admitted, while for
medical admissions more of the
branching takes place after admission.
For these reasons, the clinical
judgment of CMS’s medical staff
supports our actuaries’ estimate of the
impact of the 2-midnight policy on
program payments to hospitals.
3. Estimated IPPS/OPPS Cost Difference
for Cases That Shift Between the IPPS
and OPPS
Our actuaries assumed that the OPPS
cost for services that shift between the
OPPS and IPPS was 30 percent of the
IPPS cost, and the beneficiary is
responsible for 20 percent of the OPPS
cost. The 30 percent is an assumption
about the difference on average. While
payment under the OPPS is on average
less than payment under the IPPS for
these cases, the key question is how
much less on average? For any given
case, the payment differential will vary.
We note that when the OIG examined
the payment differential between short
inpatient stays and observation stays in
their 2013 report ‘‘Hospitals’ Use of
Observation Stays and Short Inpatient
Stays for Medicare Beneficiaries’’ (OEI–
02–12–00040), it found that on average
Medicare paid nearly three times more
for a short inpatient stay than an
observation stay (p. 12). This is
consistent with the 30 percent estimate
used in the development of the ¥0.2
percent estimate. We seek comment on
whether it is appropriate to utilize a 30
percent estimate.
D. Claims Experience Since the
Implementation of the 2-Midnight Policy
Our actuaries are currently
conducting an analysis of claims
experience for FY 2014 and FY 2015 in
light of available data, including the
MedPAR data. Because that analysis is
not yet complete, we are not proposing
in this notice with comment period to
reconsider the 0.2 percent reduction in
the FY 2014 IPPS/LTCH PPS final rule
based on the results of the claims
analysis. However, we are seeking
comment on whether we should await
the completion of the actuaries’ analysis
of FY 2014 and FY 2015 data before
resolution of this proceeding.
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We note that any potential model
revisions do not necessarily mean that
the net result of the initial modelling,
namely the ultimate ¥0.2 percent
adjustment, was incorrect. As we have
indicated since the ¥0.2 percent
estimate was developed, the
assumptions used for purposes of
reasonably estimating overall impacts
cannot be construed as absolute
statements about every individual
encounter. Under the original 2midnight policy, our actuaries did not
expect that every single surgical MS–
DRG encounter spanning less than 2
midnights would shift to the outpatient
setting, that every single medical MS–
DRG encounter would remain in the
inpatient setting, and that every single
outpatient observation stay or major
surgical encounter spanning more than
2 midnights would shift to the inpatient
setting. However, for purposes of
developing the ¥0.2 percent adjustment
estimate under the original policy, a
model where cases involving a surgical
MS–DRG spanning less than 2
midnights in the historical data shifted
to the outpatient setting, cases involving
a medical MS–DRG spanning less than
2 midnights in the historical data
remained in the inpatient setting, and
outpatient observation stays and major
surgical encounters spanning more than
2 midnights in the historical data
shifted to the inpatient setting yielded a
reasonable estimate of the net effect of
the 2-midnight policy when it was
adopted. To the extent the actual
experience might vary for each of the
individual assumptions, our actuaries
estimated that the total net effect of that
variation would not significantly impact
the estimate.
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23:35 Nov 30, 2015
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There were also factors that could not
be anticipated at the time of the initial
modelling that may influence the actual
experience, such as the prohibition on
Recovery Auditor post-payment reviews
that became effective October 1, 2013.
This prohibition might have affected
hospital behavior in unexpected ways.
Our actuaries will continue to review
the claims experience for FY 2014 and
subsequent years under the 2-midnight
policy to evaluate the assumptions
underlying the original estimate. As we
indicated in the CY 2016 OPPS/ASC
final rule, we will take the reviews into
account during future rulemaking,
including potential future rulemaking
on the issue of whether or not the policy
change that we adopted for the medical
review of inpatient hospital admissions
under Medicare Part A described in the
CY 2016 OPPS final rule will have a
differential impact on expenditures
compared to the original policy.
Although our analysis of the historical
data since the implementation of the 2midnight policy is not yet complete, and
we do not propose to reconsider the
reduction in light of that analysis at this
time, we are including this discussion
in this notice because we received many
comments on the CY 2016 OPPS
proposed rule asserting that the claims
data since the adoption of the original
2-midnight policy is inconsistent with
our original ¥0.2 percent estimate. We
continue to invite comment on this
issue. As indicated in the CY 2016
OPPS final rule, we intend to respond
to all public comments regarding the
validity of the original ¥0.2 percent
adjustment that we received in response
to the CY 2016 OPPS proposed rule as
part of these Shands remand
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75111
proceedings and publish a final notice
by March 18, 2016.
We elected to promulgate the -0.2
percent adjustment for the reasons
described in the FY 2014 IPPS/LTCH
PPS proposed and final rules and
elaborated upon in this notice with
comment period. We request comment
on all aspects of that decision, including
but not limited to the information,
assumptions, and analyses supporting
the adjustment.
III. Collection of Information
Requirements
This document does not impose
information collection requirements,
that is, reporting, recordkeeping or
third-party disclosure requirements.
Consequently, there is no need for
review by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995 (44
U.S.C. 3501 et seq.).
IV. Response to Comments
Because of the large number of public
comments we normally receive on
Federal Register documents, we are not
able to acknowledge or respond to them
individually. We will consider all
comments we receive by the date and
time specified in the ‘‘DATES’’ section
of this preamble, and, when we proceed
with a subsequent document, we will
respond to the comments in the
preamble to that document.
Dated: November 20, 2015.
Andrew M. Slavitt,
Acting Administrator, Centers for Medicare
& Medicaid Services.
Dated: November 24, 2015.
Sylvia M. Burwell,
Secretary, Department of Health and Human
Services.
E:\FR\FM\01DEN1.SGM
01DEN1
75112
Federal Register / Vol. 80, No. 230 / Tuesday, December 1, 2015 / Notices
Appendix A
BILLING CODE 4120–01–C
CA#J/
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01DEN1
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tkelley on DSK3SPTVN1PROD with NOTICES
"•l'
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Federal Register / Vol. 80, No. 230 / Tuesday, December 1, 2015 / Notices
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01DEN1
EN01DE15.064
tkelley on DSK3SPTVN1PROD with NOTICES
(in'>p
ot>d
Federal Register / Vol. 80, No. 230 / Tuesday, December 1, 2015 / Notices
Appendix B
tkelley on DSK3SPTVN1PROD with NOTICES
List of APCs Containing Major
Procedures For Purposes of the 2
Midnight Estimate
APC—APC Description
0005—Level II Needle Biopsy/
Aspiration Except Bone Marrow
0007—Level II Incision & Drainage
0008—Level III Incision and Drainage
0012—Level I Debridement &
Destruction
0017—Level V Debridement &
Destruction
0019—Level I Excision/Biopsy
0020—Level II Excision/Biopsy
0021—Level III Excision/Biopsy
0022—Level IV Excision/Biopsy
0028—Level I Breast Surgery
0029—Level II Breast Surgery
0030—Level III Breast Surgery
0037—Level IV Needle Biopsy/
Aspiration Except Bone Marrow
0041— Arthroscopy
0042—Level II Arthroscopy
0045—Bone/Joint Manipulation Under
Anesthesia
0047—Arthroplasty without Prosthesis
0048—Level I Arthroplasty or
Implantation with Prosthesis
0049—Level I Musculoskeletal
Procedures Except Hand and Foot
0050—Level II Musculoskeletal
Procedures Except Hand and Foot
0051—Level III Musculoskeletal
Procedures Except Hand and Foot
0052—Level IV Musculoskeletal
Procedures Except Hand and Foot
0053—Level I Hand Musculoskeletal
Procedures
0054—Level II Hand Musculoskeletal
Procedures
0055—Level I Foot Musculoskeletal
Procedures
0056—Level II Foot Musculoskeletal
Procedures
0057—Bunion Procedures
0062—Level I Treatment Fracture/
Dislocation
0063—Level II Treatment Fracture/
Dislocation
0064—Level III Treatment Fracture/
Dislocation
0069—Thoracoscopy
0074—Level IV Endoscopy Upper
Airway
0075—Level V Endoscopy Upper
Airway
0076—Level I Endoscopy Lower Airway
0080—Diagnostic Cardiac
Catheterization
0082—Coronary or Non-Coronary
Atherectomy
0083—Coronary Angioplasty,
Valvuloplasty, and Level I
Endovascular Revascularization
0085—Level II Electrophysiologic
Procedures
0086—Level III Electrophysiologic
Procedures
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0088—Thrombectomy
0089—Insertion/Replacement of
Permanent Pacemaker and Electrodes
0090—Level I Insertion/Replacement of
Permanent Pacemaker
0091—Level II Vascular Ligation
0092—Level I Vascular Ligation
0093—Vascular Reconstruction/Fistula
Repair without Device
0103—Miscellaneous Vascular
Procedures
0104—Transcatheter Placement of
Intracoronary Stents
0105—Repair/Revision/Removal of
Pacemakers, AICDs, or Vascular
Devices
0106—Insertion/Replacement of
Pacemaker Leads and/or Electrodes
0107—Insertion of CardioverterDefibrillator Pulse Generator
0108—Insertion/Replacement/Repair of
Cardioverter-Defibrillator System
0113—Excision Lymphatic System
0114—Thyroid/Lymphadenectomy
Procedures
0115—Cannula/Access Device
Procedures
0121—Level I Tube or Catheter Changes
or Repositioning
0130—Level I Laparoscopy
0131—Level II Laparoscopy
0132—Level III Laparoscopy
0135—Level III Skin Repair
0136—Level IV Skin Repair
0137—Level V Skin Repair
0148—Level I Anal/Rectal Procedures
0149—Level III Anal/Rectal Procedures
0150—Level IV Anal/Rectal Procedures
0152—Level I Percutaneous Abdominal
and Biliary Procedures
0153—Peritoneal and Abdominal
Procedures
0154—Hernia/Hydrocele Procedures
0160—Level I Cystourethroscopy and
other Genitourinary Procedures
0161—Level II Cystourethroscopy and
other Genitourinary Procedures
0162—Level III Cystourethroscopy and
other Genitourinary Procedures
0163—Level IV Cystourethroscopy and
other Genitourinary Procedures
0166—Level I Urethral Procedures
0168—Level II Urethral Procedures
0169—Lithotripsy
0174—Level IV Laparoscopy
0181—Level II Male Genital Procedures
0183—Level I Male Genital Procedures
0184—Prostate Biopsy
0190—Level I Hysteroscopy
0192—Level IV Female Reproductive
Proc
0193—Level V Female Reproductive
Proc
0195—Level VI Female Reproductive
Procedures
0202—Level VII Female Reproductive
Procedures
0208—Laminotomies and
Laminectomies
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75115
0220—Level I Nerve Procedures
0221—Level II Nerve Procedures
0224—Implantation of Catheter/
Reservoir/Shunt
0227—Implantation of Drug Infusion
Device
0229—Level II Endovascular
Revascularization of the Lower
Extremity
0233—Level III Anterior Segment Eye
Procedures
0234—Level IV Anterior Segment Eye
Procedures
0237—Level II Posterior Segment Eye
Procedures
0238—Level I Repair and Plastic Eye
Procedures
0239—Level II Repair and Plastic Eye
Procedures
0240—Level III Repair and Plastic Eye
Procedures
0241—Level IV Repair and Plastic Eye
Procedures
0242—Level V Repair and Plastic Eye
Procedures
0243—Strabismus/Muscle Procedures
0244—Corneal and Amniotic Membrane
Transplant
0246—Cataract Procedures with IOL
Insert
0249—Cataract Procedures without IOL
Insert
0252—Level III ENT Procedures
0253—Level IV ENT Procedures
0254—Level V ENT Procedures
0255—Level II Anterior Segment Eye
Procedures
0256—Level VI ENT Procedures
0259—Level VII ENT Procedures
0293—Level VI Anterior Segment Eye
Procedures
0319—Level III Endovascular
Revascularization of the Lower
Extremity
0384—GI Procedures with Stents
0387—Level II Hysteroscopy
0415—Level II Endoscopy Lower
Airway
0419—Level II Upper GI Procedures
0422—Level III Upper GI Procedures
0423—Level II Percutaneous Abdominal
and Biliary Procedures
0425—Level II Arthroplasty or
Implantation with Prosthesis
0427—Level II Tube or Catheter
Changes or Repositioning
0428—Level III Sigmoidoscopy and
Anoscopy
0429—Level V Cystourethroscopy and
other Genitourinary Procedures
0434—Cardiac Defect Repair
0648—Level IV Breast Surgery
0651—Complex Interstitial Radiation
Source Application
0653—Vascular Reconstruction/Fistula
Repair with Device
0654—Level II Insertion/Replacement of
Permanent Pacemaker
0655—Insertion/Replacement/
Conversion of a Permanent Dual
Chamber Pacemaker or Pacing
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0656—Transcatheter Placement of
Intracoronary Drug-Eluting Stents
0672—Level III Posterior Segment Eye
Procedures
0673—Level V Anterior Segment Eye
Procedures
0674—Prostate Cryoablation
0687—Revision/Removal of
Neurostimulator Electrodes
0688—Revision/Removal of
Neurostimulator Pulse Generator
Receiver
tkelley on DSK3SPTVN1PROD with NOTICES
Appendix C
Discussion of the Outpatient Data
This Appendix provides additional detail
on how we identified outpatient claims for
observation services or a major procedure
spanning 2 midnights or more for purposes
of estimating the shift in outpatient cases.
The comprehensive APC analysis that also
formed the basis for the 2 midnight analysis
was performed using 2011 OPPS claims of
bill type 13x extracted from the Standard
Analytic File processed through December
31, 2011 with service line charges converted
to costs per the usual OPPS cost modeling
logic. (A description of the cost modeling
logic can be found in the claims accounting
document for each year of OPPS rulemaking
and is available on our Web site at https://
www.cms.gov/Medicare/Medicare-Fee-forService-Payment/HospitalOutpatientPPS/
Hospital-Outpatient-Regulations-andNotices.html.) Similar conclusions regarding
the ¥0.2 percent estimate can be drawn by
analyzing the OPPS Limited Data Set rather
than the Standard Analytic File. The CMS
Web site at https://www.cms.gov/researchstatistics-data-and-systems/files-for-order/
limiteddatasets/HospitalOPPS.html provides
information about ordering the OPPS Limited
Data Set containing the outpatient hospital
data. In order to facilitate a claims analysis
using the claim from date and the claim
through date a new field has been added to
the OPPS Limited Data Set.
Hospital OP claims do not readily
distinguish between claims based on services
provided while the beneficiary physically
stayed at the hospital and claims where the
beneficiary received recurring services on
successive days while leaving the hospital
between services. Since only continuous
stays apply for this analysis, certain
assumptions had to be made to indirectly
estimate the body of claims for continuous
stays. Claims were trimmed to only those
whose full span of coverage (the difference of
claim-through-date and claim-from-date) was
less than 7 days. Claims with longer than a
7 day span were excluded as unlikely to
represent continuous overnight stays. Claims
were then subset to those containing
observation services or a significant
procedure, as observation services are
reported differently in those two subgroups.
To further remove recurring services during
this subsetting, claims that did not fall into
one of the following were removed from the
analysis:
• Claims containing G0378 (‘‘Hospital
observation per hr’’) and a medical visit
procedure code (status indicator of ‘‘V’’);
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• Claims containing G0379 (‘‘Direct refer
hospital observ’’), considered to be ‘‘medical
claims;’’
• Claims containing a significant OPPS
procedure code (status indicator of ‘‘S’’ or
‘‘T’’) that received Medicare payment,
considered to be ‘‘surgical claims.’’
Next, the highest cost coded services on
non-observation claims (those without G0379
or without G0378 and a medical visit
procedure) were identified. Non-observation
claims where the highest cost procedure was
not a C-code (Temporary Hospital Outpatient
PPS), a J-code (non-orally administered
medication and chemotherapy drugs), a
significant OPPS procedure code (status
indicator of ‘‘S’’ or ‘‘T’’), or a medical visit
procedure code (status indicator of ‘‘V’’) were
removed from the analysis. This removed
non-observation claims where the highest
cost service was not typical for a claim
associated with a major procedure.
Following these steps, a principal
procedure representing the primary service
driving the claim’s overall utilization was
identified for each remaining claim. For
observation claims containing both G0379
and G0378 with a medical visit procedure,
the principal procedure was identified as
G0379 or G0378 depending on which code
reports a higher line-item cost. Otherwise,
observation claims were assigned a principal
procedure of G0379 and G0378 depending on
whether G0379 or G0378 with a medical visit
procedure were respectively reported.
For non-observation claims, the principal
procedure was identified as the claim’s
significant OPPS procedure code (status
indicator of ‘‘S’’ or ‘‘T’’) with the highest
line-item cost. Non-observation claims where
the earliest service date of the principal
procedure occurred more than 5 days before
or on the same date as the claim-through-date
were removed from the analysis, as these
were assumed to represent recurring services.
Additionally, non-observation claims were
trimmed to those where the principal
procedure occurs on only a single service
date, thus removing any claim that contains
major recurring services and ensuring that
the stay is initiated with a single instance of
the major procedure.
To remove aberrant claims, each claim’s
non-observation total claim cost was then
calculated by summing the line-item costs for
all coded services and all OPPS packaged
revenue centers on the claim. Each claim’s
span of coverage was also calculated as the
number of days between the provision of the
principal service and the claim’s throughdate. The geometric mean cost was calculated
for each observation or non-observation
principal procedure using the claims’ total
cost, and those claims with unreasonable
costs (That is, claim costs above 100 times or
below 1 percent of the principal procedure
geometric mean cost) were trimmed from the
analysis.
For purposes of the 2 midnight analysis,
we then further subset the data to APCs
having a status indicator of ‘‘T’’ in order
remove services which were not relevant for
the 2 midnight analysis that is, to remove
those services that were more likely to
represent diagnostic services or minor
procedures interjected into a series of
PO 00000
Frm 00074
Fmt 4703
Sfmt 4703
recurring services, and were less likely to
trigger a ‘‘surgical’’ episode in which a
continuous stay followed the procedure. For
similar reasons, our medical officers also
removed some of the remaining APCs based
on clinical judgment that those services were
unlikely to be indicative of a continuous
protracted hospital stay. The full list of OPPS
status indicators and their definitions is
published in the OPPS/ASC proposed and
final rules each year, available on our Web
site at https://www.cms.gov/Medicare/
Medicare-Fee-for-Service-Payment/
HospitalOutpatientPPS/Hospital-OutpatientRegulations-and-Notices.html. The final list
of major procedure APCs used in the
development of the ¥0.2 percent estimate
can be found in Appendix B.
As described in section II.D of this notice,
we have also been performing an analysis of
the claims experience since the
implementation of the 2-midnight policy.
This analysis has used claims data from the
OPPS Limited Data Set. We have also been
examining similar data from our Integrated
Data Repository (see https://www.cms.gov/
Research-Statistics-Data-and-Systems/
Computer-Data-and-Systems/IDR/ for a
description of the IDR). For the purpose of
this analysis, we have used the following
claim selection criteria: the third position of
the provider number group was equal to ‘‘0’’
(short-term hospital) and the first 2 positions
of the provider number were not equal to
‘‘21’’ (excludes Maryland hospitals.)
We seek comment on the appropriate
outpatient data source to use for the ¥0.2
percent estimate and any data trims and
claims selection criteria that we should apply
to the data.
Appendix D
Discussion of the Inpatient Data
This Appendix provides additional detail
on how we identified inpatient stays
spanning less than 2 midnights for surgical
MS–DRGs for purposes of estimating the shift
in inpatient cases.
The inpatient data used in the original
¥0.2 estimate was based on data from the
CMS Integrated Data Repository (IDR) (see
https://www.cms.gov/Research-StatisticsData-and-Systems/Computer-Data-andSystems/IDR/ for a description of the IDR).
The CMS Web site at https://www.cms.gov/
Research-Statistics-Data-and-Systems/Filesfor-Order/LimitedDataSets/ provides
information about ordering the ‘‘MedPAR
Limited Data Set (LDS)-Hospital (National)’’
containing the publicly available inpatient
hospital data. At the time the original ¥0.2
percent estimate was developed, we believed
similar conclusions regarding the ¥0.2
percent estimate could be drawn using either
the IDR or the publicly available inpatient
data files. However, we did not verify this at
the time.
When we now compare the number of
inpatient stays less than 2 midnights for
surgical MS–DRGs (excluding deaths and
transfers) from the FY 2011 IDR data
available to us at the time of the original
¥0.2 estimate (claims processed through
June of 2013) to the number from the FY
2011 MedPAR data (claims processed
through March of 2013), we get
E:\FR\FM\01DEN1.SGM
01DEN1
Federal Register / Vol. 80, No. 230 / Tuesday, December 1, 2015 / Notices
approximately 360,000 stays from the IDR
data and approximately 380,000 stays from
the MedPAR data. Further complicating a
current analysis relative to the analysis
performed at that time, when we examine the
FY 2011 IDR data available to us now (claims
processed through October 2015) compared
to when the original ¥0.2 percent estimate
was developed (claims processed through
June 2013), we get approximately 340,000
stays instead of the originally estimated
360,000 stays, which we suspect is at least
partly driven by subsequent claim denials for
these cases that have occurred since the data
was examined for the original ¥0.2 percent
estimate. Because the historical MedPAR
data for a given fiscal year is not generally
refreshed after it is created, unlike the IDR
which is refreshed, there is no analogous
number to the 340,000 for the FY 2011
MedPAR.
In determining the 380,000 number from
the FY 2011 MedPAR, the following
inpatient claim selection criteria and data
trims were applied to the data. We selected
FY 2011 MedPAR claims based on a FY 2011
date of discharge where the National Claims
History (NCH) claim type code was equal to
‘‘60’’ (inpatient hospital), the third position
of the provider number group was equal to
‘‘0’’ (short-term hospital), the first 2 positions
of the provider number were not equal to
‘‘21’’ (excludes Maryland hospitals), the
destination discharge code was not equal to
‘‘30’’ (excludes still a patient), the special
unit code was blank (excludes, for example,
PPS exempt units), the GHO paid code was
not equal to ‘‘1’’ (a group health organization
has not paid the provider), the total charge
amount was greater than 0, and the IME
amount was not equal to the DRG price
amount (indicating it was not a managed care
claim).
As described in section II.D of this notice,
we have also been performing an analysis of
the claims experience since the
implementation of the 2-midnight policy.
This analysis has used data from the publicly
available MedPAR file and the IDR.
We seek comment on the appropriate
inpatient data source to use for the ¥0.2
percent estimate and any data trims and
claims selection criteria that we should apply
to the data.
[FR Doc. 2015–30486 Filed 11–30–15; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
tkelley on DSK3SPTVN1PROD with NOTICES
Proposed Information Collection
Activity; Comment Request
Title: Building Bridges and Bonds
(B3) Study: Data Collection.
VerDate Sep<11>2014
23:35 Nov 30, 2015
Jkt 238001
OMB No.: New Collection.
Description: The Administration for
Children and Families (ACF), Office of
Planning, Research and Evaluation
(OPRE) proposes to collect information
as part of the Building Bridges and
Bonds (B3) study. B3 will inform
policymakers, program operators, and
stakeholders about effective ways for
fatherhood programs to support fathers
in their parenting and employment. In
particular, partnering with programs
that serve low-income fathers to
promote responsible fatherhood, the B3
study will examine the effectiveness of
strategies used to (1) engage fathers in
program activities, (2) develop and
support parenting and co-parenting
skills, and (3) advance the employment
of disadvantaged fathers. B3 will test
innovative, evidence-informed
approaches that will be added to the
core components of fatherhood
programs and will reflect the most
recent developments in behavioral
science, adult skill-building, child
development, and other relevant
disciplines. The study will include up
to six sites and specific interventions
will vary by site.
B3 includes an impact evaluation and
a process study. The impact evaluation
will involve randomly assigning
individuals to a treatment or
comparison condition and comparing
key outcomes. In addition, the study
will collect information on employment,
criminal justice and child support
outcomes from administrative records.
These data will be used to estimate the
effects of the parenting or employment
intervention on a range of outcomes
including employment; earnings; child
support; father/child contact, shared
activities, and relationship quality;
father’s commitment to his child,
parenting skills, and parenting efficacy;
co-parenting relationship quality; and
criminal justice outcomes.
The process study will describe and
document each newly established
intervention and how it operated to
provide insight into the treatment
differentials and the context for
interpreting findings of the impact
study. The process study will also
highlight lessons to the field including
what it takes to engage participants, the
challenges sites face when
implementing the parenting or
employment intervention, and the
participants’ perspectives on whether
PO 00000
Frm 00075
Fmt 4703
Sfmt 4703
75117
the program components offered met
their needs.
Data collection instruments for the B3
study include the following: (1)
Screening for program eligibility to help
ensure that only eligible fathers enroll
in the study.
(2) nFORM management information
system (MIS) to record study and
participation information. Note: Only
B3-specific burden is included with this
request. All Responsible Fatherhood
Grantees (funded by the ACF Office of
Family Assistance) are required to use
nFORM. nFORM is being developed by
the Fatherhood and Marriage Local
Evaluation and Cross-site (FaMLE Crosssite) Project and burden for these sites
are captured under OMB #0970–0460.
(3) Applicant characteristics and
program operations data for one nongrantee site. We expect most of the B3
sites will be federally funded
Responsible Fatherhood grantees, but it
is possible that one site will not and
therefore, this request includes burden
for one site to use nFORM. (4) Baseline
and follow-up surveys for the impact
study. There will be two versions of
each survey, specific to the intervention
tested. (5) Baseline and follow-up
questionnaires, interviews, focus
groups, and surveys to inform the
process study; these will also be specific
to the intervention tested.
The sites that are part of the B3 study
will use a slightly modified version of
nFORM that includes B–3 specific
information, such as: (1) B3-specific
enrollment data (2) B3-specific
information about focal child and coparent in in sites testing a parenting
intervention, and (3) B3 tracking of
child and co-parent attendance in
services with the father for program
group members in sites testing a
parenting intervention.
RESPONDENTS: Fathers seeking
services from one of the six Responsible
Fatherhood Programs in the B3 study
and staff members working at the B3
sites.
E:\FR\FM\01DEN1.SGM
01DEN1
Agencies
[Federal Register Volume 80, Number 230 (Tuesday, December 1, 2015)]
[Notices]
[Pages 75107-75117]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-30486]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-1658-NC]
RIN 0938-ZB23
Medicare Program; Inpatient Prospective Payment Systems; 0.2
Percent Reduction
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: In accordance with the Court's October 6, 2015 order in Shands
Jacksonville Medical Center, Inc., et al. v. Burwell, No. 14-263
(D.D.C.) and consolidated cases that challenge the 0.2 percent
reduction in inpatient prospective payment systems (IPPS) rates to
account for the estimated $220 million in additional FY 2014
expenditures resulting from the 2-midnight policy, this notice
discusses the basis for the 0.2 percent reduction and its underlying
assumptions and invites comments on the same in order to facilitate our
further consideration of the FY 2014 reduction. We will consider and
respond to the comments received in response to this notice, and to
comments already received on this issue in a final notice to be
published by March 18, 2016.
DATES: Comment date: To be assured consideration, comments must be
received at one of the addresses provided below, no later than 5 p.m.
e.s.t. on February 2, 2016.
ADDRESSES: In commenting, refer to file code CMS-1658-NC. Because of
staff and resource limitations, we cannot accept comments by facsimile
(FAX) transmission.
You may submit comments in one of four ways (please choose only one
of the ways listed):
1. Electronically. You may submit electronic comments on this
notice to https://www.regulations.gov. Follow the ``Submit a comment''
instructions.
2. By regular mail. You may mail written comments to the following
address ONLY: Centers for Medicare & Medicaid Services, Department of
Health and Human Services, Attention: CMS-1658-NC, P.O. Box 8013,
Baltimore, MD 21244-8013.
Please allow sufficient time for mailed comments to be received
before the close of the comment period.
3. By express or overnight mail. You may send written comments to
the following address ONLY: Centers for Medicare & Medicaid Services,
Department of Health and Human Services, Attention: CMS-1658-NC, Mail
Stop C4-26-05, 7500 Security Boulevard, Baltimore, MD 21244-1850.
4. By hand or courier. Alternatively, you may deliver (by hand or
courier) your written comments ONLY to the following addresses:
a. For delivery in Washington, DC--Centers for Medicare & Medicaid
Services, Department of Health and Human Services, Room 445-G, Hubert
H. Humphrey Building, 200 Independence Avenue SW., Washington, DC
20201.
(Because access to the interior of the Hubert H. Humphrey Building
is not readily available to persons without Federal government
identification, commenters are encouraged to leave their comments in
the CMS drop slots located in the main lobby of the building. A stamp-
in clock is available for persons wishing to retain a proof of filing
by stamping in and retaining an extra copy of the comments being
filed.)
b. For delivery in Baltimore, MD--Centers for Medicare & Medicaid
Services, Department of Health and Human Services, 7500 Security
Boulevard, Baltimore, MD 21244-1850.
If you intend to deliver your comments to the Baltimore address,
call telephone number (410) 786-9994 in advance to schedule your
arrival with one of our staff members.
Comments erroneously mailed to the addresses indicated as
appropriate for hand or courier delivery may be delayed and received
after the comment period.
For information on viewing public comments, see the beginning of
the SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Ing-Jye Cheng, (410) 786-2260 or Don
Thompson, 410-786-6504.
SUPPLEMENTARY INFORMATION: Inspection of Public Comments: All comments
received before the close of the comment period are available for
viewing by the public, including any personally identifiable or
confidential business information that is included in a comment. We
post all comments received before the close of the comment period on
the following Web site as soon as possible after they have
[[Page 75108]]
been received: https://www.regulations.gov. Follow the search
instructions on that Web site to view public comments.
Comments received timely will also be available for public
inspection as they are received, generally beginning approximately 3
weeks after publication of a document, at the headquarters of the
Centers for Medicare & Medicaid Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday through Friday of each week from 8:30
a.m. to 4 p.m. e.s.t. To schedule an appointment to view public
comments, phone 1-800-743-3951.
I. Background
In the final rule titled ``Medicare Program; Hospital Inpatient
Prospective Payment Systems for the Acute Care Hospitals and the Long-
Term Care Hospital Prospective Payment System and Final Fiscal Year
2014 Rates; Quality Reporting Requirements for Specific Providers;
Hospital Conditions of Participation; Payment Policies Related to
Patient Status'' (hereinafter referred to as the FY 2014 IPPS/LTCH PPS
final rule), we adopted the 2-midnight policy effective October 1, 2013
(78 FR 50906 through 50954). Under the 2-midnight policy, an inpatient
admission is generally appropriate for Medicare Part A payment if the
physician (or other qualified practitioner) admits the patient as an
inpatient based upon the expectation that the patient will need
hospital care that crosses at least 2 midnights. In assessing the
expected duration of necessary care, the physician (or other
practitioner) may take into account outpatient hospital care received
prior to inpatient admission. If the patient is expected to need less
than 2 midnights of care in the hospital, the services furnished should
generally be billed as outpatient services. Our actuaries estimated
that the 2-midnight policy would increase expenditures by approximately
$220 million in FY 2014 due to an expected net increase in inpatient
encounters. We used our authority under section 1886(d)(5)(I)(i) of the
Act to make a reduction of 0.2 percent to the standardized amount, the
Puerto Rico standardized amount, and the hospital-specific payment
rate, and we used our authority under section 1886(g) of the Act to
make a reduction of 0.2 percent to the national capital Federal rate
and the Puerto Rico-specific capital rate, in order to offset this
estimated $220 million in additional IPPS expenditures in FY 2014. (In
addition to an operating IPPS payment for each discharge, hospitals
also receive a capital IPPS payment for each discharge so a net
increase in the number of inpatient encounters also results in
increased expenditures under the capital IPPS.)
II. Supplemental Notice Requesting Comments on the FY 2014 IPPS Rule
A. Overview
As noted in section I. of this notice with comment period, we
estimated based on an actuarial model that the 2-midnight policy would
increase IPPS expenditures by approximately $220 million in FY 2014 due
to an expected net increase in inpatient encounters, as described in
greater detail in an August 19, 2013 memorandum. (See Appendix A of
this notice.)
Section II.B. of this notice with comment period provides
additional details on the calculation of this estimate (that is, what
we did) and section II.C. of this notice with comment period discusses
the actuaries' assumptions, including why those assumptions were
reasonable. We collectively refer to the calculations and assumptions
as the actuarial ``model'' for estimating the financial impact of the
policy change. Section II.D. of this notice with comment period
discusses the status of an analysis currently being conducted by our
actuaries of the claims experience since the implementation of the 2-
midnight policy. We seek comment on all aspects of the model used by
our actuaries, including but not limited to those for which we
specifically request comment. We seek comment on, and will consider
comments on, all aspects of the 0.2 percent reduction.
B. Calculation of the Impact of the 2-Midnight Policy
The task of modeling the impact of the 2-midnight policy on
hospital payments begins with a recognition that some cases that were
previously outpatient cases will become inpatient cases and vice versa.
Therefore, our actuaries were required to develop a model that
determined the net effect of the number of cases that would move in
each direction.
In estimating the number of outpatient cases that would shift to
the inpatient setting, we analyzed calendar year (CY) 2011 claims that
included spending for observation care or a major procedure. For the
purposes of the -0.2 percent estimate, CMS physicians defined
observation care as Outpatient Prospective Payment System (OPPS) claims
containing Healthcare Common Procedure Coding System (HCPCS) code
``G0378'', Hospital observation service, per hour, or HCPCS code
``G0379'' Direct admission of patient for hospital observation care. We
used the difference between the first date of service for the HCPCS
code (generally the first date that the service represented by that
code was provided to the patient) and the ``claim through'' date
(generally the last date any service on the claim was provided to the
patient) to determine the length of the observation care. In this
manner, we identified approximately 350,000 observation care stays of 2
midnights or more using the CY 2011 claims.
A list of the Ambulatory Payment Classifications (APCs) containing
the major procedures used in the determination of the -0.2 percent
estimate can be found in Appendix B of this notice with comment period.
As with observation care, the difference between the first date of
service for the HCPCS code and the claim through date was used to
determine the length of the major procedure. We identified
approximately 50,000 claims containing major procedures with stays
lasting 2 midnights or more using the CY 2011 claims.
Combining the observation care and the major procedures resulted in
approximately 400,000 claims for services of 2 midnights or more from
the CY 2011 claims data.
For additional details on the identification of the outpatient
claims, see Appendix C of this notice with comment period.
In estimating the number of inpatient stays that would shift to the
outpatient setting, FY 2011 inpatient claims containing a surgical
Medicare Severity Diagnosis Related Group (MS-DRG) were analyzed. The
number of these stays that spanned less than 2 midnights, based on the
length of stay, was approximately 360,000. FY 2009 and FY 2010 data
were also analyzed and the results were consistent with the FY 2011
results.
For additional details on the identification of the inpatient
claims, see Appendix D of this notice with comment period.
Our actuaries also assumed that payment under the OPPS would be 30
percent of the payment under the IPPS for encounters shifting between
the two systems, and that the beneficiary is responsible for 20 percent
of the Part B cost.
The number of short stay discharges (for this purpose, same day
discharges and discharges crossing one or two midnights) represented
about 28 percent of total discharges in FY 2011, and approximately 17
percent of total spending for the total discharges. The assumed net
increase of 40,000
[[Page 75109]]
inpatient discharges (= 400,000 OPPS to IPPS--360,000 IPPS to OPPS)
represented an increase of 1.2 percent in the number of short stay
discharges. Taking 1.2 percent of 17 percent of total spending results
in the estimate at the time of the FY 2014 IPPS/LTCH PPS rulemaking
that the 2-midnight policy would result in an additional $290 million
in inpatient expenditures, as shown for FY 2014 in the table ``Impact
on Medicare Expenditures'' found in the memorandum in Appendix A of
this notice. The estimates for the additional inpatient expenditures
for FYs 2015 through 2018 can also be found in the table (for example,
$320 million for FY 2015).
For the outpatient expenditure estimate, taking 30 percent (based
on the assumption that payment under the OPPS would be 30 percent of
the payment under the IPPS) of 80 percent (to account for the assumed
20 percent beneficiary responsibility) of the $290 million inpatient
estimate results in approximately $70 million less outpatient
expenditures. The estimates for the reduction in outpatient
expenditures for FYs 2015 through 2018 can also be found in the table
(For example, $80 million for FY 2015.)
The estimated $290 million increase in inpatient expenditures less
the estimated $70 million decrease in outpatient expenditures yields
the estimated net impact by our actuaries at the time of the FY 2014
IPPS/LTCH PPS rulemaking of an additional $220 million in expenditures
in FY 2014 as a result of the 2-midnight policy. The estimated
additional expenditures for FYs 2015 through 2018 can be similarly
calculated.
Using the information contained in this section and the appendices
to this notice, interested members of the public should be able to
calculate the estimate by our actuaries of an additional $220 million
in expenditures in FY 2014 as a result of the 2-midnight policy. (For
interested members of the public who wish to perform this calculation,
we highlight the discussion in Appendix D regarding the number of
inpatient cases identified in the MedPAR data and the Integrated Data
Repository.)
C. Discussion of the Assumptions Made in the Calculation of the Impact
of the 2-Midnight Policy
As our actuaries stated in the August 2013 memorandum, the
estimates depend critically on the assumed utilization changes in the
inpatient and outpatient hospital settings. We discuss the assumptions
underlying the estimates further in this section.
1. Estimated Outpatient Cases That Would Shift to the Inpatient Setting
As indicated previously, in estimating the number of outpatient
cases that would shift to the inpatient setting, CY 2011 claims that
included spending for observation care or a major procedure were
analyzed. This was done in order to remove claims with diagnostic
services or minor procedures that would be less likely to trigger an
encounter in which there was a continuous stay. (See the discussion in
Appendix C of this notice with comment period.)
For the purpose of the -0.2 percent estimate, observation care was
defined as OPPS claims containing HCPCS ``G0378,'' Hospital observation
service, per hour, or ``G0379'' Direct admission of patient for
hospital observation care. At the time the -0.2 percent estimate was
being developed, we were also examining establishing comprehensive APCs
under the OPPS (for a summary of the results of this examination see
the CY 2014 OPPS proposed rule (78 FR 43540)). One of the claims
analyses that we developed for this purpose included service counts of
G0378 and G0379 and significant procedures. Since this analysis
included the universe of services of interest for the 2-midnight policy
at that time, it was well-suited for use in the development of the -0.2
percent estimate as well. For a discussion of the data specifications
for this claims analysis, and how it was subset for the 2-midnight
analysis, see Appendix C of this notice with comment period.
However, in retrospect, using HCPCS G0378 and G0379 may have been
an overly conservative definition of observation services, because not
every use of observation services would be captured by the G-codes. As
indicated in the Medicare Claims Processing Manual,\1\ hospitals are
required to report observation charges under the revenue center code
``0760'', Treatment or observation room--general classification, or
``0762'' Treatment or observation room--observation room regardless of
whether or not the G-codes are billed.
---------------------------------------------------------------------------
\1\ See section 290.2.1 in Chapter 4 of the Medicare Claims
Processing Manual available at https://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/downloads/clm104c04.pdf)
---------------------------------------------------------------------------
We also note that the Office of the Inspector General (OIG) used
this revenue center code definition of observation services in its
report ``Hospitals' Use of Observation Stays and Short Inpatient Stays
\2\ (OEI-02-12-00040).
---------------------------------------------------------------------------
\2\ Available at https://oig.hhs.gov/oei/reports/oei-02-12-00040.pdf.
---------------------------------------------------------------------------
If we had defined observation services using revenue center codes
0760 and 0762 instead of HCPCS codes G0378 and G0379, we would have
identified approximately 400,000 claims for observation services
spanning 2 midnights or more (instead of 350,000) and we would have
estimated approximately 450,000 cases shifting from the outpatient to
the inpatient setting (400,000 claims for observation stays spanning
more than 2 midnights and approximately 50,000 claims for major
procedures) instead of the 400,000 cases used in the estimate. We seek
comment on whether it would be more appropriate to define observation
services using revenue center codes 0760 and 0762 rather than HCPCS
codes G0378 and G0379.
Another consequence of the use of the claims analyses that we
developed for the purpose of the comprehensive APCs involves the
approach used to determine whether observation stays spanned 2
midnights or more. In general, in the claims analysis for comprehensive
APC development, we examined the difference between the date of service
for the primary HCPCS code on the claim and the claim through date. For
the observation services in this analysis, we used the difference
between first date of service for the observation service and the claim
through date to determine the length of the observation case. However,
in retrospect, as with the definition of observation services, this may
have been an overly conservative approach to determining the length of
the observation case. Under the 2-midnight policy, for purposes of
determining whether the 2 midnight benchmark was met and, therefore,
whether inpatient admission was generally appropriate, the expected
duration of care includes the time the beneficiary spent receiving
outpatient services within the hospital. This includes services such as
observation services, treatments in the emergency department, and
procedures provided in the operating room or other treatment area. It
is not just the time spent receiving observation services. As such, it
may have been more appropriate to have used the ``claim from'' date (in
general the date that the beneficiary entered the hospital), rather
than the first date that observation services were provided in order to
determine when claims containing observation services spanned 2
midnights or more. If we had used such an approach when developing the
original estimate, instead of approximately 350,000 claims with
observation services spanning 2
[[Page 75110]]
midnights or more, the estimate would have been approximately 430,000
claims under the HCPCS code G0378/G0370 definition of observation
services and approximately 520,000 under the revenue center code 0760/
0762 definition of observation services. When combined with our
estimate of major procedures, we would have estimated as many as
570,000 cases shifting from the outpatient to the inpatient setting
under this approach instead of the 400,000 cases used in the estimate.
We seek comment on whether it would be more appropriate to have used
the claim from date rather than the first date that observation
services were provided in order to determine when claims containing
observation services spanned 2 midnights or more.
2. Estimated Inpatient Cases That Would Shift to the Outpatient Setting
We believed some proportion of the inpatient cases under 2
midnights in the historical data would remain inpatient because we
believed that behavioral changes by hospitals and admitting
practitioners would mitigate some of the impact of cases shifting
between the inpatient hospital setting and the outpatient hospital
setting. The question was how to reasonably estimate what that
proportion would be for purposes of modelling the impact of the 2-
midnight policy. We believe that a model distinguishing between medical
and surgical cases is a reasonable approach to use in determining what
proportion of inpatient cases would remain in the inpatient setting and
what proportion would shift to the outpatient setting.
Specifically, in estimating the number of inpatient stays that
would shift to the outpatient setting, FY 2011 inpatient claims
containing a surgical MS-DRG were analyzed. Our actuaries assumed that
those spanning less than 2 midnights (other than those stays that were
cut short by a death or transfer) would shift from the inpatient
setting to the outpatient setting. Stays that were cut short by a death
or transfer were excluded because under the 2-midnight policy those
cases would generally be considered to be appropriately treated on an
inpatient basis. (For a discussion of the data specifications for the
inpatient claims analysis, see Appendix D of this notice.)
Claims containing medical MS-DRGs were excluded because, as stated
in the August 2013 memorandum, ``it was assumed that these cases would
be unaffected by the policy change.'' Our actuaries excluded medical
MS-DRGs when developing the -0.2 percent estimate because they believed
that due to behavioral changes by hospitals and admitting practitioners
most inpatient medical encounters spanning less than 2 midnights before
the current 2-midnight policy was implemented might be reasonably
expected to extend past 2 midnights after its implementation and would
thus still be considered inpatient. They believed that the clinical
assessments and protocols used by physicians to develop an expected
length of stay for medical cases were, in general, more variable and
less defined than those used to develop an expected length of stay for
surgical cases.
Evidence of this medical/surgical dichotomy is seen in proprietary
utilization review tools such as the Milliman Care Guidelines, which
are guidelines based originally on actuarial data, and InterQual, which
are clinically oriented guidelines. Both tools reflect the same types
of distinctions between medical and surgical cases that we assumed
based on CMS medical staff's clinical judgment. Although all
guidelines, and all surgeons, advise patients that individual patients
vary in their post-operative courses, there are predictable post-
operative courses that are based on such factors as whether or not the
abdominal cavity or the pleural cavity are entered, the expected time
for recovery from anesthesia, the expected time to resume urinary
function, the expected time to resume bowel function, the expected time
to regain mobility, and the typical period for common post-operative
interventions. These are by no means absolute but are fairly well-
defined, as evidenced by the surgeon's ability to generally inform the
patient, within a day or so, how long the patient probably can expect
to remain in the hospital if treatment goes well. Part of this
decreased variance is due to the fact that the reason for admission, a
specific surgical procedure, is well-defined.
Conversely, for medical admissions a single diagnosis typically
covers a much broader spectrum of possibilities. Pneumonia may have
different etiologies, with vastly different expected lengths of stay. A
stroke may be minor, allowing a brief diagnostic workup to be followed
by outpatient rehabilitation, or catastrophic, triggering a prolonged
stay before stabilization and discharge. Chronic obstructive pulmonary
disease (COPD) and congestive heart failure (CHF) may respond rapidly
to medication adjustments or may result in Intense Care Unit (ICU)
stays. Unlike the surgical procedure, the medical diagnosis does not
imply a reasonably consistent set of activities. In fact, typical
medical protocols are highly branched, with the initial portion of
hospital care typically focused on diagnostics that serve to
differentiate patient subsets that define treatments and simultaneously
suggest different hospital courses. The increased variability in the
medical protocols is influenced by the fact that, for planned surgical
admissions, more of the branching takes place in the process of
selecting a specific surgical intervention before the patient is
admitted, while for medical admissions more of the branching takes
place after admission.
For these reasons, the clinical judgment of CMS's medical staff
supports our actuaries' estimate of the impact of the 2-midnight policy
on program payments to hospitals.
3. Estimated IPPS/OPPS Cost Difference for Cases That Shift Between the
IPPS and OPPS
Our actuaries assumed that the OPPS cost for services that shift
between the OPPS and IPPS was 30 percent of the IPPS cost, and the
beneficiary is responsible for 20 percent of the OPPS cost. The 30
percent is an assumption about the difference on average. While payment
under the OPPS is on average less than payment under the IPPS for these
cases, the key question is how much less on average? For any given
case, the payment differential will vary. We note that when the OIG
examined the payment differential between short inpatient stays and
observation stays in their 2013 report ``Hospitals' Use of Observation
Stays and Short Inpatient Stays for Medicare Beneficiaries'' (OEI-02-
12-00040), it found that on average Medicare paid nearly three times
more for a short inpatient stay than an observation stay (p. 12). This
is consistent with the 30 percent estimate used in the development of
the -0.2 percent estimate. We seek comment on whether it is appropriate
to utilize a 30 percent estimate.
D. Claims Experience Since the Implementation of the 2-Midnight Policy
Our actuaries are currently conducting an analysis of claims
experience for FY 2014 and FY 2015 in light of available data,
including the MedPAR data. Because that analysis is not yet complete,
we are not proposing in this notice with comment period to reconsider
the 0.2 percent reduction in the FY 2014 IPPS/LTCH PPS final rule based
on the results of the claims analysis. However, we are seeking comment
on whether we should await the completion of the actuaries' analysis of
FY 2014 and FY 2015 data before resolution of this proceeding.
[[Page 75111]]
We note that any potential model revisions do not necessarily mean
that the net result of the initial modelling, namely the ultimate -0.2
percent adjustment, was incorrect. As we have indicated since the -0.2
percent estimate was developed, the assumptions used for purposes of
reasonably estimating overall impacts cannot be construed as absolute
statements about every individual encounter. Under the original 2-
midnight policy, our actuaries did not expect that every single
surgical MS-DRG encounter spanning less than 2 midnights would shift to
the outpatient setting, that every single medical MS-DRG encounter
would remain in the inpatient setting, and that every single outpatient
observation stay or major surgical encounter spanning more than 2
midnights would shift to the inpatient setting. However, for purposes
of developing the -0.2 percent adjustment estimate under the original
policy, a model where cases involving a surgical MS-DRG spanning less
than 2 midnights in the historical data shifted to the outpatient
setting, cases involving a medical MS-DRG spanning less than 2
midnights in the historical data remained in the inpatient setting, and
outpatient observation stays and major surgical encounters spanning
more than 2 midnights in the historical data shifted to the inpatient
setting yielded a reasonable estimate of the net effect of the 2-
midnight policy when it was adopted. To the extent the actual
experience might vary for each of the individual assumptions, our
actuaries estimated that the total net effect of that variation would
not significantly impact the estimate.
There were also factors that could not be anticipated at the time
of the initial modelling that may influence the actual experience, such
as the prohibition on Recovery Auditor post-payment reviews that became
effective October 1, 2013. This prohibition might have affected
hospital behavior in unexpected ways.
Our actuaries will continue to review the claims experience for FY
2014 and subsequent years under the 2-midnight policy to evaluate the
assumptions underlying the original estimate. As we indicated in the CY
2016 OPPS/ASC final rule, we will take the reviews into account during
future rulemaking, including potential future rulemaking on the issue
of whether or not the policy change that we adopted for the medical
review of inpatient hospital admissions under Medicare Part A described
in the CY 2016 OPPS final rule will have a differential impact on
expenditures compared to the original policy. Although our analysis of
the historical data since the implementation of the 2-midnight policy
is not yet complete, and we do not propose to reconsider the reduction
in light of that analysis at this time, we are including this
discussion in this notice because we received many comments on the CY
2016 OPPS proposed rule asserting that the claims data since the
adoption of the original 2-midnight policy is inconsistent with our
original -0.2 percent estimate. We continue to invite comment on this
issue. As indicated in the CY 2016 OPPS final rule, we intend to
respond to all public comments regarding the validity of the original -
0.2 percent adjustment that we received in response to the CY 2016 OPPS
proposed rule as part of these Shands remand proceedings and publish a
final notice by March 18, 2016.
We elected to promulgate the -0.2 percent adjustment for the
reasons described in the FY 2014 IPPS/LTCH PPS proposed and final rules
and elaborated upon in this notice with comment period. We request
comment on all aspects of that decision, including but not limited to
the information, assumptions, and analyses supporting the adjustment.
III. Collection of Information Requirements
This document does not impose information collection requirements,
that is, reporting, recordkeeping or third-party disclosure
requirements. Consequently, there is no need for review by the Office
of Management and Budget under the authority of the Paperwork Reduction
Act of 1995 (44 U.S.C. 3501 et seq.).
IV. Response to Comments
Because of the large number of public comments we normally receive
on Federal Register documents, we are not able to acknowledge or
respond to them individually. We will consider all comments we receive
by the date and time specified in the ``DATES'' section of this
preamble, and, when we proceed with a subsequent document, we will
respond to the comments in the preamble to that document.
Dated: November 20, 2015.
Andrew M. Slavitt,
Acting Administrator, Centers for Medicare & Medicaid Services.
Dated: November 24, 2015.
Sylvia M. Burwell,
Secretary, Department of Health and Human Services.
[[Page 75112]]
Appendix A
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Appendix B
List of APCs Containing Major Procedures For Purposes of the 2 Midnight
Estimate
APC--APC Description
0005--Level II Needle Biopsy/Aspiration Except Bone Marrow
0007--Level II Incision & Drainage
0008--Level III Incision and Drainage
0012--Level I Debridement & Destruction
0017--Level V Debridement & Destruction
0019--Level I Excision/Biopsy
0020--Level II Excision/Biopsy
0021--Level III Excision/Biopsy
0022--Level IV Excision/Biopsy
0028--Level I Breast Surgery
0029--Level II Breast Surgery
0030--Level III Breast Surgery
0037--Level IV Needle Biopsy/Aspiration Except Bone Marrow
0041-- Arthroscopy
0042--Level II Arthroscopy
0045--Bone/Joint Manipulation Under Anesthesia
0047--Arthroplasty without Prosthesis
0048--Level I Arthroplasty or Implantation with Prosthesis
0049--Level I Musculoskeletal Procedures Except Hand and Foot
0050--Level II Musculoskeletal Procedures Except Hand and Foot
0051--Level III Musculoskeletal Procedures Except Hand and Foot
0052--Level IV Musculoskeletal Procedures Except Hand and Foot
0053--Level I Hand Musculoskeletal Procedures
0054--Level II Hand Musculoskeletal Procedures
0055--Level I Foot Musculoskeletal Procedures
0056--Level II Foot Musculoskeletal Procedures
0057--Bunion Procedures
0062--Level I Treatment Fracture/Dislocation
0063--Level II Treatment Fracture/Dislocation
0064--Level III Treatment Fracture/Dislocation
0069--Thoracoscopy
0074--Level IV Endoscopy Upper Airway
0075--Level V Endoscopy Upper Airway
0076--Level I Endoscopy Lower Airway
0080--Diagnostic Cardiac Catheterization
0082--Coronary or Non-Coronary Atherectomy
0083--Coronary Angioplasty, Valvuloplasty, and Level I Endovascular
Revascularization
0085--Level II Electrophysiologic Procedures
0086--Level III Electrophysiologic Procedures
0088--Thrombectomy
0089--Insertion/Replacement of Permanent Pacemaker and Electrodes
0090--Level I Insertion/Replacement of Permanent Pacemaker
0091--Level II Vascular Ligation
0092--Level I Vascular Ligation
0093--Vascular Reconstruction/Fistula Repair without Device
0103--Miscellaneous Vascular Procedures
0104--Transcatheter Placement of Intracoronary Stents
0105--Repair/Revision/Removal of Pacemakers, AICDs, or Vascular Devices
0106--Insertion/Replacement of Pacemaker Leads and/or Electrodes
0107--Insertion of Cardioverter-Defibrillator Pulse Generator
0108--Insertion/Replacement/Repair of Cardioverter-Defibrillator System
0113--Excision Lymphatic System
0114--Thyroid/Lymphadenectomy Procedures
0115--Cannula/Access Device Procedures
0121--Level I Tube or Catheter Changes or Repositioning
0130--Level I Laparoscopy
0131--Level II Laparoscopy
0132--Level III Laparoscopy
0135--Level III Skin Repair
0136--Level IV Skin Repair
0137--Level V Skin Repair
0148--Level I Anal/Rectal Procedures
0149--Level III Anal/Rectal Procedures
0150--Level IV Anal/Rectal Procedures
0152--Level I Percutaneous Abdominal and Biliary Procedures
0153--Peritoneal and Abdominal Procedures
0154--Hernia/Hydrocele Procedures
0160--Level I Cystourethroscopy and other Genitourinary Procedures
0161--Level II Cystourethroscopy and other Genitourinary Procedures
0162--Level III Cystourethroscopy and other Genitourinary Procedures
0163--Level IV Cystourethroscopy and other Genitourinary Procedures
0166--Level I Urethral Procedures
0168--Level II Urethral Procedures
0169--Lithotripsy
0174--Level IV Laparoscopy
0181--Level II Male Genital Procedures
0183--Level I Male Genital Procedures
0184--Prostate Biopsy
0190--Level I Hysteroscopy
0192--Level IV Female Reproductive Proc
0193--Level V Female Reproductive Proc
0195--Level VI Female Reproductive Procedures
0202--Level VII Female Reproductive Procedures
0208--Laminotomies and Laminectomies
0220--Level I Nerve Procedures
0221--Level II Nerve Procedures
0224--Implantation of Catheter/Reservoir/Shunt
0227--Implantation of Drug Infusion Device
0229--Level II Endovascular Revascularization of the Lower Extremity
0233--Level III Anterior Segment Eye Procedures
0234--Level IV Anterior Segment Eye Procedures
0237--Level II Posterior Segment Eye Procedures
0238--Level I Repair and Plastic Eye Procedures
0239--Level II Repair and Plastic Eye Procedures
0240--Level III Repair and Plastic Eye Procedures
0241--Level IV Repair and Plastic Eye Procedures
0242--Level V Repair and Plastic Eye Procedures
0243--Strabismus/Muscle Procedures
0244--Corneal and Amniotic Membrane Transplant
0246--Cataract Procedures with IOL Insert
0249--Cataract Procedures without IOL Insert
0252--Level III ENT Procedures
0253--Level IV ENT Procedures
0254--Level V ENT Procedures
0255--Level II Anterior Segment Eye Procedures
0256--Level VI ENT Procedures
0259--Level VII ENT Procedures
0293--Level VI Anterior Segment Eye Procedures
0319--Level III Endovascular Revascularization of the Lower Extremity
0384--GI Procedures with Stents
0387--Level II Hysteroscopy
0415--Level II Endoscopy Lower Airway
0419--Level II Upper GI Procedures
0422--Level III Upper GI Procedures
0423--Level II Percutaneous Abdominal and Biliary Procedures
0425--Level II Arthroplasty or Implantation with Prosthesis
0427--Level II Tube or Catheter Changes or Repositioning
0428--Level III Sigmoidoscopy and Anoscopy
0429--Level V Cystourethroscopy and other Genitourinary Procedures
0434--Cardiac Defect Repair
0648--Level IV Breast Surgery
0651--Complex Interstitial Radiation Source Application
0653--Vascular Reconstruction/Fistula Repair with Device
0654--Level II Insertion/Replacement of Permanent Pacemaker
0655--Insertion/Replacement/Conversion of a Permanent Dual Chamber
Pacemaker or Pacing
[[Page 75116]]
0656--Transcatheter Placement of Intracoronary Drug-Eluting Stents
0672--Level III Posterior Segment Eye Procedures
0673--Level V Anterior Segment Eye Procedures
0674--Prostate Cryoablation
0687--Revision/Removal of Neurostimulator Electrodes
0688--Revision/Removal of Neurostimulator Pulse Generator Receiver
Appendix C
Discussion of the Outpatient Data
This Appendix provides additional detail on how we identified
outpatient claims for observation services or a major procedure
spanning 2 midnights or more for purposes of estimating the shift in
outpatient cases.
The comprehensive APC analysis that also formed the basis for
the 2 midnight analysis was performed using 2011 OPPS claims of bill
type 13x extracted from the Standard Analytic File processed through
December 31, 2011 with service line charges converted to costs per
the usual OPPS cost modeling logic. (A description of the cost
modeling logic can be found in the claims accounting document for
each year of OPPS rulemaking and is available on our Web site at
https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/HospitalOutpatientPPS/Hospital-Outpatient-Regulations-and-Notices.html.) Similar conclusions regarding the -0.2 percent
estimate can be drawn by analyzing the OPPS Limited Data Set rather
than the Standard Analytic File. The CMS Web site at https://www.cms.gov/research-statistics-data-and-systems/files-for-order/limiteddatasets/HospitalOPPS.html provides information about
ordering the OPPS Limited Data Set containing the outpatient
hospital data. In order to facilitate a claims analysis using the
claim from date and the claim through date a new field has been
added to the OPPS Limited Data Set.
Hospital OP claims do not readily distinguish between claims
based on services provided while the beneficiary physically stayed
at the hospital and claims where the beneficiary received recurring
services on successive days while leaving the hospital between
services. Since only continuous stays apply for this analysis,
certain assumptions had to be made to indirectly estimate the body
of claims for continuous stays. Claims were trimmed to only those
whose full span of coverage (the difference of claim-through-date
and claim-from-date) was less than 7 days. Claims with longer than a
7 day span were excluded as unlikely to represent continuous
overnight stays. Claims were then subset to those containing
observation services or a significant procedure, as observation
services are reported differently in those two subgroups. To further
remove recurring services during this subsetting, claims that did
not fall into one of the following were removed from the analysis:
Claims containing G0378 (``Hospital observation per
hr'') and a medical visit procedure code (status indicator of
``V'');
Claims containing G0379 (``Direct refer hospital
observ''), considered to be ``medical claims;''
Claims containing a significant OPPS procedure code
(status indicator of ``S'' or ``T'') that received Medicare payment,
considered to be ``surgical claims.''
Next, the highest cost coded services on non-observation claims
(those without G0379 or without G0378 and a medical visit procedure)
were identified. Non-observation claims where the highest cost
procedure was not a C-code (Temporary Hospital Outpatient PPS), a J-
code (non-orally administered medication and chemotherapy drugs), a
significant OPPS procedure code (status indicator of ``S'' or
``T''), or a medical visit procedure code (status indicator of
``V'') were removed from the analysis. This removed non-observation
claims where the highest cost service was not typical for a claim
associated with a major procedure.
Following these steps, a principal procedure representing the
primary service driving the claim's overall utilization was
identified for each remaining claim. For observation claims
containing both G0379 and G0378 with a medical visit procedure, the
principal procedure was identified as G0379 or G0378 depending on
which code reports a higher line-item cost. Otherwise, observation
claims were assigned a principal procedure of G0379 and G0378
depending on whether G0379 or G0378 with a medical visit procedure
were respectively reported.
For non-observation claims, the principal procedure was
identified as the claim's significant OPPS procedure code (status
indicator of ``S'' or ``T'') with the highest line-item cost. Non-
observation claims where the earliest service date of the principal
procedure occurred more than 5 days before or on the same date as
the claim-through-date were removed from the analysis, as these were
assumed to represent recurring services. Additionally, non-
observation claims were trimmed to those where the principal
procedure occurs on only a single service date, thus removing any
claim that contains major recurring services and ensuring that the
stay is initiated with a single instance of the major procedure.
To remove aberrant claims, each claim's non-observation total
claim cost was then calculated by summing the line-item costs for
all coded services and all OPPS packaged revenue centers on the
claim. Each claim's span of coverage was also calculated as the
number of days between the provision of the principal service and
the claim's through-date. The geometric mean cost was calculated for
each observation or non-observation principal procedure using the
claims' total cost, and those claims with unreasonable costs (That
is, claim costs above 100 times or below 1 percent of the principal
procedure geometric mean cost) were trimmed from the analysis.
For purposes of the 2 midnight analysis, we then further subset
the data to APCs having a status indicator of ``T'' in order remove
services which were not relevant for the 2 midnight analysis that
is, to remove those services that were more likely to represent
diagnostic services or minor procedures interjected into a series of
recurring services, and were less likely to trigger a ``surgical''
episode in which a continuous stay followed the procedure. For
similar reasons, our medical officers also removed some of the
remaining APCs based on clinical judgment that those services were
unlikely to be indicative of a continuous protracted hospital stay.
The full list of OPPS status indicators and their definitions is
published in the OPPS/ASC proposed and final rules each year,
available on our Web site at https://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/HospitalOutpatientPPS/Hospital-Outpatient-Regulations-and-Notices.html. The final list of major procedure APCs
used in the development of the -0.2 percent estimate can be found in
Appendix B.
As described in section II.D of this notice, we have also been
performing an analysis of the claims experience since the
implementation of the 2-midnight policy. This analysis has used
claims data from the OPPS Limited Data Set. We have also been
examining similar data from our Integrated Data Repository (see
https://www.cms.gov/Research-Statistics-Data-and-Systems/Computer-Data-and-Systems/IDR/ for a description of the IDR). For the purpose
of this analysis, we have used the following claim selection
criteria: the third position of the provider number group was equal
to ``0'' (short-term hospital) and the first 2 positions of the
provider number were not equal to ``21'' (excludes Maryland
hospitals.)
We seek comment on the appropriate outpatient data source to use
for the -0.2 percent estimate and any data trims and claims
selection criteria that we should apply to the data.
Appendix D
Discussion of the Inpatient Data
This Appendix provides additional detail on how we identified
inpatient stays spanning less than 2 midnights for surgical MS-DRGs
for purposes of estimating the shift in inpatient cases.
The inpatient data used in the original -0.2 estimate was based
on data from the CMS Integrated Data Repository (IDR) (see https://www.cms.gov/Research-Statistics-Data-and-Systems/Computer-Data-and-Systems/IDR/ for a description of the IDR). The CMS Web site at
https://www.cms.gov/Research-Statistics-Data-and-Systems/Files-for-Order/LimitedDataSets/ provides information about ordering the
``MedPAR Limited Data Set (LDS)-Hospital (National)'' containing the
publicly available inpatient hospital data. At the time the original
-0.2 percent estimate was developed, we believed similar conclusions
regarding the -0.2 percent estimate could be drawn using either the
IDR or the publicly available inpatient data files. However, we did
not verify this at the time.
When we now compare the number of inpatient stays less than 2
midnights for surgical MS-DRGs (excluding deaths and transfers) from
the FY 2011 IDR data available to us at the time of the original -
0.2 estimate (claims processed through June of 2013) to the number
from the FY 2011 MedPAR data (claims processed through March of
2013), we get
[[Page 75117]]
approximately 360,000 stays from the IDR data and approximately
380,000 stays from the MedPAR data. Further complicating a current
analysis relative to the analysis performed at that time, when we
examine the FY 2011 IDR data available to us now (claims processed
through October 2015) compared to when the original -0.2 percent
estimate was developed (claims processed through June 2013), we get
approximately 340,000 stays instead of the originally estimated
360,000 stays, which we suspect is at least partly driven by
subsequent claim denials for these cases that have occurred since
the data was examined for the original -0.2 percent estimate.
Because the historical MedPAR data for a given fiscal year is not
generally refreshed after it is created, unlike the IDR which is
refreshed, there is no analogous number to the 340,000 for the FY
2011 MedPAR.
In determining the 380,000 number from the FY 2011 MedPAR, the
following inpatient claim selection criteria and data trims were
applied to the data. We selected FY 2011 MedPAR claims based on a FY
2011 date of discharge where the National Claims History (NCH) claim
type code was equal to ``60'' (inpatient hospital), the third
position of the provider number group was equal to ``0'' (short-term
hospital), the first 2 positions of the provider number were not
equal to ``21'' (excludes Maryland hospitals), the destination
discharge code was not equal to ``30'' (excludes still a patient),
the special unit code was blank (excludes, for example, PPS exempt
units), the GHO paid code was not equal to ``1'' (a group health
organization has not paid the provider), the total charge amount was
greater than 0, and the IME amount was not equal to the DRG price
amount (indicating it was not a managed care claim).
As described in section II.D of this notice, we have also been
performing an analysis of the claims experience since the
implementation of the 2-midnight policy. This analysis has used data
from the publicly available MedPAR file and the IDR.
We seek comment on the appropriate inpatient data source to use
for the -0.2 percent estimate and any data trims and claims
selection criteria that we should apply to the data.
[FR Doc. 2015-30486 Filed 11-30-15; 8:45 am]
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