TRICARE Bundled Payment for Lower Extremity Joint Replacement or Reattachment (LEJR) Surgeries Based on Centers for Medicare and Medicaid Services (CMS) Comprehensive Care for Joint Replacement (CJR) Model, 17159-17161 [2016-06859]
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Federal Register / Vol. 81, No. 59 / Monday, March 28, 2016 / Notices
[FR Doc. 2016–06937 Filed 3–25–16; 8:45 am]
BILLING CODE 5001–06–C
DEPARTMENT OF DEFENSE
Office of the Secretary
TRICARE Bundled Payment for Lower
Extremity Joint Replacement or
Reattachment (LEJR) Surgeries Based
on Centers for Medicare and Medicaid
Services (CMS) Comprehensive Care
for Joint Replacement (CJR) Model
Department of Defense.
Notice of demonstration.
AGENCY:
ACTION:
This notice is to advise
interested parties of a Military Health
System (MHS) demonstration project
under the authority of Title 10, United
States Code, Section 1092, entitled
TRICARE Bundled Payment for Lower
Extremity Joint Replacement or
Reattachment (LEJR) Surgeries that will
test bundled payment and quality
measurement on an ‘‘episode of care’’
basis to encourage hospitals, physicians,
and post-acute care providers to work
together to improve the quality and
coordination of care from the initial
hospitalization through recovery. This
demonstration is being conducted in
compliance with Section 726 of the
National Defense Authorization Act
(NDAA) for 2016. This particular
TRICARE demonstration will be based
on Centers for Medicare and Medicaid
Services’ (CMS) Comprehensive Care for
Joint Replacement (CJR) Model, which
will be implemented in 67 metropolitan
statistical areas (MSAs) beginning April
1, 2016. CMS’s CJR Model is designed
to promote better and more efficient
care for beneficiaries undergoing LEJR
surgery (DRG 469 (major joint
replacement or reattachment of lower
extremity with major complications or
comorbidities) or 470 (major joint
replacement or reattachment of lower
extremity without major complications
or comorbidities)). Participant hospitals
in the CMS model will be held
financially accountable for the quality
and cost of the entire episode of care,
which begins with hospital admission of
a beneficiary and ends 90 days postdischarge in order to cover all related
costs for the complete recovery period.
This ‘‘bundled’’ episode includes all
related items and services paid under
Medicare Part A and Part B for all
Medicare fee-for-service beneficiaries.
The TRICARE demonstration project
will test this value-based payment
model in the Tampa-St. Petersburg MSA
for DRG 470 only (including 90 days of
related post-operative care) to assess
whether value-driven bundled payment
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SUMMARY:
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incentives will result in a reduction in
the rate of increase in health care
spending and improvements in health
care quality, patient experience of care,
and overall health of TRICARE
beneficiaries. All network and nonnetwork hospitals with at least 20
TRICARE admissions for DRG 470 over
the three years of Fiscal Year (FY) 2013,
2014, and 2015 shall be required to
participate in the demonstration project
(excluding admissions for beneficiaries
with primary Other Health Insurance
(OHI), Active Duty Service Members
(ADSMs), and Medicare-TRICARE dual
eligible beneficiaries). Once selected for
participation, hospitals will remain in
the project throughout the duration of
this demonstration (regardless of actual
TRICARE utilization) unless the
Government directs otherwise.
DATES: Effective Date: This
demonstration is mandated by Section
726 of the National Defense
Authorization Act for Fiscal Year 2016,
with an implementation deadline of
May 23, 2016. This demonstration
authority will remain in effect until
December 31, 2019.
ADDRESSES: Defense Health Agency,
Health Plan Execution and Operations,
7700 Arlington Boulevard, Suite 5101,
Falls Church, Virginia 22042.
FOR FURTHER INFORMATION CONTACT: For
questions pertaining to this
demonstration, please contact Ms. Debra
Hatzel at (303) 676–3572.
SUPPLEMENTARY INFORMATION:
A. Background
Section 726 of the National Defense
Authorization Act (NDAA) for Fiscal
Year 2016 directed the Department of
Defense to conduct a demonstration
project on incentives to improve health
care provided under the TRICARE
program, also known as paying for value
rather than for volume or value-based
reimbursement. Innovative health care
payment models are being tested and
implemented by the CMS and a variety
of commercial health care programs and
insurers. This demonstration will assess
whether value-driven incentives will
result in a reduction in the rate of
increase in health care spending and
improvements in health care quality,
patient experience of care, and overall
health of TRICARE beneficiaries.
This demonstration program is based
on the Medicare Program for
Comprehensive Care for Joint
Replacement (CJR) Payment Model for
Acute Care Hospitals Furnishing Lower
Extremity Joint Replacement Services,
under the authority of the Center for
Medicare and Medicaid Innovation
(CMMI) pursuant to section 1115A of
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Fmt 4703
Sfmt 4703
17159
the Social Security Act, and as
implemented by CMS. A copy of the
Final Rule published by CMS on
November 24, 2015, may be found at
https://www.federalregister.gov/articles/
2015/11/24/2015-29438/medicareprogram-comprehensive-care-for-jointreplacement-payment-model-for-acutecare-hospitals. In general, CMS sought
to target high expenditure, high
utilization procedures for which there
were significant regional variation in
spending. Acute care hospitals, as the
site of surgery, will be held accountable
for spending during the entire episode
of care. This model seeks to promote the
alignment of financial and other
incentives for all health care providers
and suppliers caring for a beneficiary
during an LEJR episode, thereby
improving quality and increasing
efficiency in the provision of care. It is
also anticipated the CJR model will
benefit Medicare beneficiaries by
improving coordination and transition
of care by incentivizing more efficient
service delivery and higher value care
across the inpatient and post-acute care
spectrum spanning the episode of care.
The CMS CJR model will be
implemented in 67 metropolitan
statistical areas (MSAs) beginning April
1, 2016. Under Medicare, this episodebased payment model is mandatory for
all hospitals in the designated MSAs.
The Department of Defense elected to
conduct a demonstration project to
adapt, in general, and test this valuebased incentive program to assess
whether a reduction in the rate of
increase in health care spending can be
achieved while simultaneously
improving the experience and quality of
health care provided to our beneficiaries
by providing financial incentives for
high-quality, efficient care. Consistent
with the CJR model, TRICARE
demonstration hospitals will be held
accountable for the costs and quality of
the entire episode of care and will be
afforded the opportunity to earn
performance-based payments by
appropriately reducing expenditures
and meeting certain quality metrics.
An analysis of LEJR surgeries in the
TRICARE beneficiary population was
conducted. This analysis revealed some
of the Metropolitan Service Areas
(MSAs) participating in the CMS
Comprehensive Care for Joint
Replacement (CJR) model have a
substantial number of TRICARE-eligible
beneficiaries. These locations include
the Killeen-Temple TX MSA, the
Seattle-Tacoma WA MSA, and the
Tampa-St. Petersburg FL MSA. Both the
Killeen-Temple MSA and the SeattleTacoma MSA are associated with large
inpatient military treatment facilities
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Federal Register / Vol. 81, No. 59 / Monday, March 28, 2016 / Notices
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(MTFs); however, there are not any
inpatient MTFs associated with the
Tampa-St. Petersburg MSA. Based on
FY 2015 data, there are 74,133 TRICARE
eligibles residing in the Tampa-St.
Petersburg area, and 128 joint
replacement or reattachment surgeries
for TRICARE beneficiaries were
performed in FY 2015. Due to colocation with CMS’s MSA (which makes
hospital participation mandatory), the
significant number of TRICARE eligible
beneficiaries receiving joint replacement
or reattachment surgeries, and the lack
of MTF inpatient resources, Tampa-St.
Petersburg was selected for this
demonstration project. Additionally, it
was determined only one to two percent
of all TRICARE LEJR patients are in
DRG 469 (major joint replacement or
reattachment of lower extremity with
major complications or comorbidities).
As a result, the TRICARE demonstration
project will exclude DRG 469
admissions since there are insufficient
volumes for setting target episode prices
for these procedures.
B. Description of the Demonstration
Project
All network and non-network
hospitals in the Tampa-St. Petersburg
area will be required to participate in
the demonstration if they had at least 20
TRICARE admissions for DRG 470 over
the three years of FY 2013, FY 2014, and
FY 2015 (excluding admissions for
beneficiaries with Other Health
Insurance (OHI), Active Duty Service
Members (ADSMs), and MedicareTRICARE dual eligible beneficiaries).
Once selected for participation,
demonstration hospitals will remain in
the program throughout the duration of
this NDAA demonstration (regardless of
actual TRICARE utilization) unless the
Government directs otherwise.
Demonstration hospitals will be
accountable for quality and cost of care
for an inpatient stay that results in DRG
470, along with all related care provided
during the 90-day period following
discharge.
The Defense Health Agency (DHA)
will prospectively establish target
episode prices for each demonstration
hospital at least 30 days prior to the
start of each demonstration year. This
target episode price shall be based on
TRICARE claims for DRG 470
admissions and associated postoperative care for FY 2013, FY 2014,
and FY 2015, and shall be a blend of
hospital-specific and market-wide
historical episode costs. This historical
data period shall be used for the
duration of the demonstration, with
annual adjustments for inflation. In
Demonstration Years one and two, the
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Jkt 238001
blended rate for the target episode price
shall be developed with two-thirds
hospital-specific data and one-third
market-wide data; in Demonstration
Year three, the target episode price shall
be developed with one-third hospitalspecific data and two-thirds marketwide data.
Although the CMS CJR Model
incorporates an automatic cost savings
of 3percent into their target episode
prices, DHA will not deduct an
automatic cost savings amount when
developing TRICARE target episode
prices. Instead, target episode pricing
will take historical network discounts,
DRG and CPT pricing adjustments, and
annual inflation factors into
consideration. Additionally, the value of
any care provided in the direct care
system will not be considered in
developing target prices. This will
permit local military treatment facilities
to recapture, where appropriate, postsurgery outpatient care under existing
TRICARE procedures based on the
MTF’s capability and capacity without
affecting incentive calculations. The
target episode price will clearly indicate
the cost build-up calculations for each
component of care within the episode.
These target episode prices will become
the basis for calculating any incentive
payments or penalties.
For purposes of this demonstration,
Demonstration Year one will commence
for admissions on May 23, 2016, and
will include all completed episodes
with an end date continuing through
September 30, 2017 (including the full
90 days post-discharge period).
Subsequent demonstration years will be
conducted on a fiscal year basis (i.e., for
episodes ending October 1st through
September 30th). The target episode
price in effect on the date of hospital
admission shall be used for incentive
calculation purposes, even if a portion
of post-discharge care is delivered in the
subsequent demonstration year.
During each demonstration year, all
hospital, physician, and post-acute care
claims will be paid under the normal
TRICARE reimbursement
methodologies. At the end of each
demonstration year, the total costs of all
completed episodes for the year will be
compared to the aggregate target episode
price for each demonstration hospital to
determine whether actual costs were
less than, equal to, or greater than the
target episode price. In order to ensure
all costs are properly attributed to each
demonstration hospital, actual cost
calculations shall occur no sooner than
90 calendar days following the end of
the demonstration year to allow
adequate time for claims processing. In
order to encourage use of the direct care
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Sfmt 4703
system and because the managed care
support contractor processing the
episode calculations will not have
access to direct care cost data, costs for
direct care shall be excluded (consistent
with the target cost development).
In addition to performing these cost
calculations, DHA will utilize the
composite quality score (as determined
by CMS) for each demonstration
hospital as the basis for determining
eligibility for gain-sharing. This
composite quality score is a hospitallevel summary quality score reflecting
performance and improvement on the
quality measures adopted for the
Medicare CJR model (Total Hip
Arthroplasty (THA)/Total Knee
Arthroplasty (TKA)) complications
measure and the Hospital Consumer
Assessment of Healthcare Providers and
Systems (HCAHPS) patient experience
survey measure. TRICARE will use
Hospital Compare as the source for
these data. Hospitals that do not achieve
and maintain a favorable CJR composite
quality score for the full demonstration
year are not eligible for incentive
payments, regardless of whether cost
savings are achieved. TRICARE is
following the same approach as
Medicare in order to ensure hospitals
are not reducing the quality of care
offered to beneficiaries or reducing
patients’ overall perception of their
hospital experience.
Incentive payments will be calculated
using the CMS gain/loss sharing model;
beginning in Demonstration Year one,
positive incentive payments will be
made to hospitals who achieve and
maintain a favorable CJR composite
quality score for the full demonstration
year and who demonstrate cost savings
as compared to the target episode price.
‘‘Downside’’ risk (negative financial
incentives) will not be phased into the
payment model until the second
demonstration year. Gain/Loss sharing
will increase over time, from no loss
sharing in Demonstration Year one (only
gain sharing), to higher levels in later
years (gain sharing of 5 percent in
Demonstration Years one and two, and
10 percent in Demonstration Year
three). Loss sharing is 0 in
Demonstration Year one, 5 percent in
Demonstration Year two, and 10 percent
in Demonstration Year three.
On a quarterly basis, demonstration
hospitals will receive feedback from the
MCSCs on their current quality
performance (as identified in Hospital
Compare), episode of care costs to date,
and projected eligibility for incentives
(based on TRICARE claims and
Medicare’s composite quality scores for
each hospital). To facilitate effective
communication with demonstration
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Federal Register / Vol. 81, No. 59 / Monday, March 28, 2016 / Notices
hospitals, these quarterly reports shall
mirror the format and detail of CMS’s
feedback reports to the extent feasible.
Active Duty Service Members (ADSMs),
Medicare-TRICARE Dual Eligible
(TDEFIC) beneficiaries, and
beneficiaries with Other Health
Insurance (OHI) are excluded from this
demonstration.
C. Communications
The DHA will proactively educate
beneficiaries, providers, and other
stakeholders about this change.
D. Evaluation
This demonstration project will assist
the Department in evaluating whether
value-driven incentives will result in a
reduction in the rate of increase in
health care spending and improvements
in health care quality, patient
experience of care, and overall health of
TRICARE beneficiaries. Regular status
reports and a full analysis of
demonstration outcomes will be
conducted consistent with the
requirements in Section 726 of the 2016
NDAA. Future expansions of the
demonstration project to additional
locations may be considered based on
DHA data analysis for the Tampa-St.
Petersburg market. Details of any future
expansions will be announced via
Federal Register notice prior to
implementation.
Dated: March 22, 2016.
Aaron Siegel,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. 2016–06859 Filed 3–25–16; 8:45 am]
BILLING CODE 5001–06–P
DEPARTMENT OF EDUCATION
[Docket No.: ED–2016–ICCD–0009]
Agency Information Collection
Activities; Submission to the Office of
Management and Budget for Review
and Approval; Comment Request;
Campus Equity in Athletics Disclosure
Act (EADA) Survey
Office of Postsecondary
Education (OPE), Department of
Education (ED).
ACTION: Notice.
AGENCY:
In accordance with the
Paperwork Reduction Act of 1995 (44
U.S.C. chapter 3501 et seq.), ED is
proposing an extension of an existing
information collection.
DATES: Interested persons are invited to
submit comments on or before April 27,
2016.
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SUMMARY:
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To access and review all the
documents related to the information
collection listed in this notice, please
use https://www.regulations.gov by
searching the Docket ID number ED–
2016–ICCD–0009. Comments submitted
in response to this notice should be
submitted electronically through the
Federal eRulemaking Portal at https://
www.regulations.gov by selecting the
Docket ID number or via postal mail,
commercial delivery, or hand delivery.
Please note that comments submitted by
fax or email and those submitted after
the comment period will not be
accepted. Written requests for
information or comments submitted by
postal mail or delivery should be
addressed to the Director of the
Information Collection Clearance
Division, U.S. Department of Education,
400 Maryland Avenue SW., LBJ, Room
2E–103, Washington, DC 20202–4537.
ADDRESSES:
For
specific questions related to collection
activities, please contact Ashley
Higgins, 202–219–7061.
FOR FURTHER INFORMATION CONTACT:
The
Department of Education (ED), in
accordance with the Paperwork
Reduction Act of 1995 (PRA) (44 U.S.C.
3506(c)(2)(A)), provides the general
public and Federal agencies with an
opportunity to comment on proposed,
revised, and continuing collections of
information. This helps the Department
assess the impact of its information
collection requirements and minimize
the public’s reporting burden. It also
helps the public understand the
Department’s information collection
requirements and provide the requested
data in the desired format. ED is
soliciting comments on the proposed
information collection request (ICR) that
is described below. The Department of
Education is especially interested in
public comment addressing the
following issues: (1) Is this collection
necessary to the proper functions of the
Department; (2) will this information be
processed and used in a timely manner;
(3) is the estimate of burden accurate;
(4) how might the Department enhance
the quality, utility, and clarity of the
information to be collected; and (5) how
might the Department minimize the
burden of this collection on the
respondents, including through the use
of information technology. Please note
that written comments received in
response to this notice will be
considered public records.
Title of Collection: Campus Equity in
Athletics Disclosure Act (EADA)
Survey.
OMB Control Number: 1840–0827.
SUPPLEMENTARY INFORMATION:
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17161
Type of Review: An extension of an
existing information collection.
Respondents/Affected Public: State,
Local, and Tribal Governments; Private
Sector.
Total Estimated Number of Annual
Responses: 2,072.
Total Estimated Number of Annual
Burden Hours: 11,397.
Abstract: The collection of
information is necessary under section
485 of the Higher Education Act of
1965, as amended, with the goal of
increasing transparency surrounding
college athletics for student, prospective
students, parents, employees and the
general public. The survey is a
collection tool to compile the annual
data on college athletics. The data
collected from the individual
institutions by ED and is made available
to the public through the Equity in
Athletics Data Analysis Cutting Tool as
well as the College Navigator.
Dated: March 23, 2016.
Kate Mullan,
Acting Director, Information Collection
Clearance Division, Office of the Chief Privacy
Officer, Office of Management.
[FR Doc. 2016–06890 Filed 3–25–16; 8:45 am]
BILLING CODE 4000–01–P
DEPARTMENT OF ENERGY
[FE Docket No. 16–29–LNG]
Cheniere Marketing, LLC; Application
for Blanket Authorization To Export
Previously Imported Liquefied Natural
Gas on a Short-Term Basis
Office of Fossil Energy, DOE.
Notice of application.
AGENCY:
ACTION:
The Office of Fossil Energy
(FE) of the Department of Energy (DOE)
gives notice of receipt of an application
(Application), filed on March 7, 2016,
by Cheniere Marketing, LLC (CMI),
requesting blanket authorization to
export liquefied natural gas (LNG)
previously imported into the United
States from foreign sources in an
amount up to the equivalent of 500
billion cubic feet (Bcf) of natural gas on
a short-term or spot market basis for a
two-year period commencing on June 7,
2016.1 CMI seeks authorization to
export the LNG from the Sabine Pass
LNG terminal owned by Sabine Pass
LNG, L.P. located in Cameron Parish,
Louisiana, to any country with the
capacity to import LNG via ocean-going
carrier and with which trade is not
SUMMARY:
1 CMI’s current blanket authorization to export
previously imported LNG, granted in DOE/FE Order
No. 3442 on June 6, 2014, extends through June 6,
2016.
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Agencies
[Federal Register Volume 81, Number 59 (Monday, March 28, 2016)]
[Notices]
[Pages 17159-17161]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-06859]
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
Office of the Secretary
TRICARE Bundled Payment for Lower Extremity Joint Replacement or
Reattachment (LEJR) Surgeries Based on Centers for Medicare and
Medicaid Services (CMS) Comprehensive Care for Joint Replacement (CJR)
Model
AGENCY: Department of Defense.
ACTION: Notice of demonstration.
-----------------------------------------------------------------------
SUMMARY: This notice is to advise interested parties of a Military
Health System (MHS) demonstration project under the authority of Title
10, United States Code, Section 1092, entitled TRICARE Bundled Payment
for Lower Extremity Joint Replacement or Reattachment (LEJR) Surgeries
that will test bundled payment and quality measurement on an ``episode
of care'' basis to encourage hospitals, physicians, and post-acute care
providers to work together to improve the quality and coordination of
care from the initial hospitalization through recovery. This
demonstration is being conducted in compliance with Section 726 of the
National Defense Authorization Act (NDAA) for 2016. This particular
TRICARE demonstration will be based on Centers for Medicare and
Medicaid Services' (CMS) Comprehensive Care for Joint Replacement (CJR)
Model, which will be implemented in 67 metropolitan statistical areas
(MSAs) beginning April 1, 2016. CMS's CJR Model is designed to promote
better and more efficient care for beneficiaries undergoing LEJR
surgery (DRG 469 (major joint replacement or reattachment of lower
extremity with major complications or comorbidities) or 470 (major
joint replacement or reattachment of lower extremity without major
complications or comorbidities)). Participant hospitals in the CMS
model will be held financially accountable for the quality and cost of
the entire episode of care, which begins with hospital admission of a
beneficiary and ends 90 days post-discharge in order to cover all
related costs for the complete recovery period. This ``bundled''
episode includes all related items and services paid under Medicare
Part A and Part B for all Medicare fee-for-service beneficiaries. The
TRICARE demonstration project will test this value-based payment model
in the Tampa-St. Petersburg MSA for DRG 470 only (including 90 days of
related post-operative care) to assess whether value-driven bundled
payment incentives will result in a reduction in the rate of increase
in health care spending and improvements in health care quality,
patient experience of care, and overall health of TRICARE
beneficiaries. All network and non-network hospitals with at least 20
TRICARE admissions for DRG 470 over the three years of Fiscal Year (FY)
2013, 2014, and 2015 shall be required to participate in the
demonstration project (excluding admissions for beneficiaries with
primary Other Health Insurance (OHI), Active Duty Service Members
(ADSMs), and Medicare-TRICARE dual eligible beneficiaries). Once
selected for participation, hospitals will remain in the project
throughout the duration of this demonstration (regardless of actual
TRICARE utilization) unless the Government directs otherwise.
DATES: Effective Date: This demonstration is mandated by Section 726 of
the National Defense Authorization Act for Fiscal Year 2016, with an
implementation deadline of May 23, 2016. This demonstration authority
will remain in effect until December 31, 2019.
ADDRESSES: Defense Health Agency, Health Plan Execution and Operations,
7700 Arlington Boulevard, Suite 5101, Falls Church, Virginia 22042.
FOR FURTHER INFORMATION CONTACT: For questions pertaining to this
demonstration, please contact Ms. Debra Hatzel at (303) 676-3572.
SUPPLEMENTARY INFORMATION:
A. Background
Section 726 of the National Defense Authorization Act (NDAA) for
Fiscal Year 2016 directed the Department of Defense to conduct a
demonstration project on incentives to improve health care provided
under the TRICARE program, also known as paying for value rather than
for volume or value-based reimbursement. Innovative health care payment
models are being tested and implemented by the CMS and a variety of
commercial health care programs and insurers. This demonstration will
assess whether value-driven incentives will result in a reduction in
the rate of increase in health care spending and improvements in health
care quality, patient experience of care, and overall health of TRICARE
beneficiaries.
This demonstration program is based on the Medicare Program for
Comprehensive Care for Joint Replacement (CJR) Payment Model for Acute
Care Hospitals Furnishing Lower Extremity Joint Replacement Services,
under the authority of the Center for Medicare and Medicaid Innovation
(CMMI) pursuant to section 1115A of the Social Security Act, and as
implemented by CMS. A copy of the Final Rule published by CMS on
November 24, 2015, may be found at https://www.federalregister.gov/articles/2015/11/24/2015-29438/medicare-program-comprehensive-care-for-joint-replacement-payment-model-for-acute-care-hospitals. In general,
CMS sought to target high expenditure, high utilization procedures for
which there were significant regional variation in spending. Acute care
hospitals, as the site of surgery, will be held accountable for
spending during the entire episode of care. This model seeks to promote
the alignment of financial and other incentives for all health care
providers and suppliers caring for a beneficiary during an LEJR
episode, thereby improving quality and increasing efficiency in the
provision of care. It is also anticipated the CJR model will benefit
Medicare beneficiaries by improving coordination and transition of care
by incentivizing more efficient service delivery and higher value care
across the inpatient and post-acute care spectrum spanning the episode
of care. The CMS CJR model will be implemented in 67 metropolitan
statistical areas (MSAs) beginning April 1, 2016. Under Medicare, this
episode-based payment model is mandatory for all hospitals in the
designated MSAs.
The Department of Defense elected to conduct a demonstration
project to adapt, in general, and test this value-based incentive
program to assess whether a reduction in the rate of increase in health
care spending can be achieved while simultaneously improving the
experience and quality of health care provided to our beneficiaries by
providing financial incentives for high-quality, efficient care.
Consistent with the CJR model, TRICARE demonstration hospitals will be
held accountable for the costs and quality of the entire episode of
care and will be afforded the opportunity to earn performance-based
payments by appropriately reducing expenditures and meeting certain
quality metrics.
An analysis of LEJR surgeries in the TRICARE beneficiary population
was conducted. This analysis revealed some of the Metropolitan Service
Areas (MSAs) participating in the CMS Comprehensive Care for Joint
Replacement (CJR) model have a substantial number of TRICARE-eligible
beneficiaries. These locations include the Killeen-Temple TX MSA, the
Seattle-Tacoma WA MSA, and the Tampa-St. Petersburg FL MSA. Both the
Killeen-Temple MSA and the Seattle-Tacoma MSA are associated with large
inpatient military treatment facilities
[[Page 17160]]
(MTFs); however, there are not any inpatient MTFs associated with the
Tampa-St. Petersburg MSA. Based on FY 2015 data, there are 74,133
TRICARE eligibles residing in the Tampa-St. Petersburg area, and 128
joint replacement or reattachment surgeries for TRICARE beneficiaries
were performed in FY 2015. Due to co-location with CMS's MSA (which
makes hospital participation mandatory), the significant number of
TRICARE eligible beneficiaries receiving joint replacement or
reattachment surgeries, and the lack of MTF inpatient resources, Tampa-
St. Petersburg was selected for this demonstration project.
Additionally, it was determined only one to two percent of all TRICARE
LEJR patients are in DRG 469 (major joint replacement or reattachment
of lower extremity with major complications or comorbidities). As a
result, the TRICARE demonstration project will exclude DRG 469
admissions since there are insufficient volumes for setting target
episode prices for these procedures.
B. Description of the Demonstration Project
All network and non-network hospitals in the Tampa-St. Petersburg
area will be required to participate in the demonstration if they had
at least 20 TRICARE admissions for DRG 470 over the three years of FY
2013, FY 2014, and FY 2015 (excluding admissions for beneficiaries with
Other Health Insurance (OHI), Active Duty Service Members (ADSMs), and
Medicare-TRICARE dual eligible beneficiaries). Once selected for
participation, demonstration hospitals will remain in the program
throughout the duration of this NDAA demonstration (regardless of
actual TRICARE utilization) unless the Government directs otherwise.
Demonstration hospitals will be accountable for quality and cost of
care for an inpatient stay that results in DRG 470, along with all
related care provided during the 90-day period following discharge.
The Defense Health Agency (DHA) will prospectively establish target
episode prices for each demonstration hospital at least 30 days prior
to the start of each demonstration year. This target episode price
shall be based on TRICARE claims for DRG 470 admissions and associated
post-operative care for FY 2013, FY 2014, and FY 2015, and shall be a
blend of hospital-specific and market-wide historical episode costs.
This historical data period shall be used for the duration of the
demonstration, with annual adjustments for inflation. In Demonstration
Years one and two, the blended rate for the target episode price shall
be developed with two-thirds hospital-specific data and one-third
market-wide data; in Demonstration Year three, the target episode price
shall be developed with one-third hospital-specific data and two-thirds
market-wide data.
Although the CMS CJR Model incorporates an automatic cost savings
of 3percent into their target episode prices, DHA will not deduct an
automatic cost savings amount when developing TRICARE target episode
prices. Instead, target episode pricing will take historical network
discounts, DRG and CPT pricing adjustments, and annual inflation
factors into consideration. Additionally, the value of any care
provided in the direct care system will not be considered in developing
target prices. This will permit local military treatment facilities to
recapture, where appropriate, post-surgery outpatient care under
existing TRICARE procedures based on the MTF's capability and capacity
without affecting incentive calculations. The target episode price will
clearly indicate the cost build-up calculations for each component of
care within the episode. These target episode prices will become the
basis for calculating any incentive payments or penalties.
For purposes of this demonstration, Demonstration Year one will
commence for admissions on May 23, 2016, and will include all completed
episodes with an end date continuing through September 30, 2017
(including the full 90 days post-discharge period). Subsequent
demonstration years will be conducted on a fiscal year basis (i.e., for
episodes ending October 1st through September 30th). The target episode
price in effect on the date of hospital admission shall be used for
incentive calculation purposes, even if a portion of post-discharge
care is delivered in the subsequent demonstration year.
During each demonstration year, all hospital, physician, and post-
acute care claims will be paid under the normal TRICARE reimbursement
methodologies. At the end of each demonstration year, the total costs
of all completed episodes for the year will be compared to the
aggregate target episode price for each demonstration hospital to
determine whether actual costs were less than, equal to, or greater
than the target episode price. In order to ensure all costs are
properly attributed to each demonstration hospital, actual cost
calculations shall occur no sooner than 90 calendar days following the
end of the demonstration year to allow adequate time for claims
processing. In order to encourage use of the direct care system and
because the managed care support contractor processing the episode
calculations will not have access to direct care cost data, costs for
direct care shall be excluded (consistent with the target cost
development).
In addition to performing these cost calculations, DHA will utilize
the composite quality score (as determined by CMS) for each
demonstration hospital as the basis for determining eligibility for
gain-sharing. This composite quality score is a hospital-level summary
quality score reflecting performance and improvement on the quality
measures adopted for the Medicare CJR model (Total Hip Arthroplasty
(THA)/Total Knee Arthroplasty (TKA)) complications measure and the
Hospital Consumer Assessment of Healthcare Providers and Systems
(HCAHPS) patient experience survey measure. TRICARE will use Hospital
Compare as the source for these data. Hospitals that do not achieve and
maintain a favorable CJR composite quality score for the full
demonstration year are not eligible for incentive payments, regardless
of whether cost savings are achieved. TRICARE is following the same
approach as Medicare in order to ensure hospitals are not reducing the
quality of care offered to beneficiaries or reducing patients' overall
perception of their hospital experience.
Incentive payments will be calculated using the CMS gain/loss
sharing model; beginning in Demonstration Year one, positive incentive
payments will be made to hospitals who achieve and maintain a favorable
CJR composite quality score for the full demonstration year and who
demonstrate cost savings as compared to the target episode price.
``Downside'' risk (negative financial incentives) will not be phased
into the payment model until the second demonstration year. Gain/Loss
sharing will increase over time, from no loss sharing in Demonstration
Year one (only gain sharing), to higher levels in later years (gain
sharing of 5 percent in Demonstration Years one and two, and 10 percent
in Demonstration Year three). Loss sharing is 0 in Demonstration Year
one, 5 percent in Demonstration Year two, and 10 percent in
Demonstration Year three.
On a quarterly basis, demonstration hospitals will receive feedback
from the MCSCs on their current quality performance (as identified in
Hospital Compare), episode of care costs to date, and projected
eligibility for incentives (based on TRICARE claims and Medicare's
composite quality scores for each hospital). To facilitate effective
communication with demonstration
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hospitals, these quarterly reports shall mirror the format and detail
of CMS's feedback reports to the extent feasible. Active Duty Service
Members (ADSMs), Medicare-TRICARE Dual Eligible (TDEFIC) beneficiaries,
and beneficiaries with Other Health Insurance (OHI) are excluded from
this demonstration.
C. Communications
The DHA will proactively educate beneficiaries, providers, and
other stakeholders about this change.
D. Evaluation
This demonstration project will assist the Department in evaluating
whether value-driven incentives will result in a reduction in the rate
of increase in health care spending and improvements in health care
quality, patient experience of care, and overall health of TRICARE
beneficiaries. Regular status reports and a full analysis of
demonstration outcomes will be conducted consistent with the
requirements in Section 726 of the 2016 NDAA. Future expansions of the
demonstration project to additional locations may be considered based
on DHA data analysis for the Tampa-St. Petersburg market. Details of
any future expansions will be announced via Federal Register notice
prior to implementation.
Dated: March 22, 2016.
Aaron Siegel,
Alternate OSD Federal Register Liaison Officer, Department of Defense.
[FR Doc. 2016-06859 Filed 3-25-16; 8:45 am]
BILLING CODE 5001-06-P