Medicare Program; Medicare Shared Savings Program: Accountable Care Organizations, 19528-19654 [2011-7880]
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19528
Federal Register / Vol. 76, No. 67 / Thursday, April 7, 2011 / Proposed Rules
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 425
[CMS–1345–P]
RIN 0938–AQ22
Medicare Program; Medicare Shared
Savings Program: Accountable Care
Organizations
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
AGENCY:
This proposed rule would
implement section 3022 of the
Affordable Care Act which contains
provisions relating to Medicare
payments to providers of services and
suppliers participating in Accountable
Care Organizations (ACOs). Under these
provisions, providers of services and
suppliers can continue to receive
traditional Medicare fee-for-service
payments under Parts A and B, and be
eligible for additional payments based
on meeting specified quality and
savings requirements.
DATES: To be assured consideration,
comments must be received at one of
the addresses provided below, no later
than 5 p.m. on June 6, 2011.
ADDRESSES: In commenting, please refer
to file code CMS–1345–P. 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 regulation
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–1345–P, 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–1345–P, Mail
Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
4. By hand or courier. If you prefer,
you may deliver (by hand or courier)
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your written comments before the close
of the comment period to either of 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,
please call telephone number (410) 786–
7195 in advance to schedule your
arrival with one of our staff members.
Comments mailed to the addresses
indicated as appropriate for hand or
courier delivery may be delayed and
received after the comment period.
Submission of comments on
paperwork requirements. You may
submit comments on this document’s
paperwork requirements by following
the instructions at the end of the
‘‘Collection of Information
Requirements’’ section in this document.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Dr.
Terri Postma (410)786–8084.
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
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,
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Baltimore, Maryland 21244, Monday
through Friday of each week from 8:30
a.m. to 4 p.m. To schedule an
appointment to view public comments,
phone 1–800–743–3951.
Table of Contents
To assist readers in referencing
sections contained in this preamble, we
are providing a table of contents.
I. Background
A. Introduction and Overview of ValueBased Purchasing
B. Statutory Basis for the Medicare Shared
Savings Program
C. Overview and Intent of the Medicare
Shared Savings Program
D. Related Affordable Care Act Provisions
1. Establishment of Center for Medicare
and Medicaid Innovation (Innovation
Center)
2. Independence at Home Medical
Practices
3. State Option To Provide Health Homes
4. Community Health Teams
E. Related Ongoing CMS Efforts
1. Physician Group Practice Demonstration
2. Medicare Health Care Quality
Demonstration
II. Provisions of the Proposed Rule
A. Organizations of the Proposed Rule
B. Eligibility and Governance
1. Eligible Entities
2. Legal Structure and Governance
a. Legal Entity
b. Governance
c. Composition of the Governing Body
3. Leadership and Management Structure
4. Accountability for Beneficiaries
5. Agreement Requirement
6. Distribution of Savings
7. Sufficient Number of Primary Care
Providers and Beneficiaries
8. Required Reporting on Participating
ACO Professionals
9. Processes To Promote Evidence-Based
Medicine, Patient Engagement,
Reporting, and Coordination of Care
a. Processes To Promote Evidence-Based
Medicine
b. Processes To Promote Patient
Engagement
c. Processes To Report on Quality and Cost
Measures
d. Processes To Promote Coordination of
Care
10. Patient Centeredness Criteria
a. Beneficiary Experience of Care Survey
b. Patient Involvement in Governance
c. Evaluation of Population Health Needs
and Consideration of Diversity
d. Implementation of Individualize Care
Plans and Integration of Community
Resources
11. ACO Marketing Guidelines
12. Program Integrity Requirements
a. Compliance Plans
b. Compliance With Program Requirements
c. Conflicts of Interest
d. Screening of ACO Applicants
e. Prohibition on Certain Required
Referrals and Cost Shifting
C. Establishing the 3-YearAgreement With
the Secretary
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1. Options for Start Date of the
Performance Year
2. Timing and Process for Evaluating
Shared Savings
3. Data Sharing
4. Sharing Aggregate Data
5. Identification of Historically Assigned
Beneficiaries
6. Sharing Beneficiary Identifiable Claims
Data
a. Legal Authority To Provide Beneficiary
Identifiable Data to ACOs
(1) Sharing Data Related to Medicare Parts
A and B
(2) Sharing Data Related to Medicare Part
D
b. Beneficiary Opportunity To Opt Out of
Claims Data Sharing
7. New Program Standards Established
During 3-Year Agreement Period
8. Managing Significant Changes to the
ACO During the Agreement Period
9. Future Participation of Previously
Terminated Program Participants
D. Assignment of Medicare Fee-For-Service
Beneficiaries
1. Operational Identification of an ACO
2. Definition of Primary Care Services
3. Prospective vs. Retrospective Beneficiary
Assignment to Calculate Eligibility for
Shared Savings
4. Majority vs. Plurality Rule for
Beneficiary Assignment
5. Beneficiary Information and Notification
E. Quality and Other Reporting
Requirements
1. Introduction
2. Proposed Measures To Assess the
Quality of Care Furnished by an ACO
a. General
b. Considerations in Selecting Measures
1. Use of Measures
2. Scoring Methodology
c. Proposed Quality Measures for Use in
Establishing Quality Performance
Standards that ACOs Must Meet for
Shared Savings
3. Requirements for Quality Measures Data
Submission by ACOs
a. General
b. GPRO Tool
c. Certified EHR Technology
4. Quality Performance Standards
a. General
b. Option 1—Performance Scoring
(1) Measure Domains and Measures
Included in the Domains
(2) Methodology for Calculating a
Performance Score for Each Measure
Within a Domain
(3) Methodology for Calculating a
Performance Score for Each Domain
(4) The Quality Performance Standard
Level
c. Option 2—Quality Threshold
(1) Minimum Quality Threshold
(2) Considerations in Establishing a Quality
Threshold
5. Incorporation of Other Reporting
Requirements Related to the Physician
Quality Reporting System and Electronic
Health Records Technology Under
Section 1848 of the Act
6. Public Reporting
7. Aligning ACO Quality Measures with
other Laws and Regulations
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F. Shared Savings Determination
1. Background
2. Overview of Shared Savings
Determination
3. Establishing an Expenditure Benchmark
a. Background
b. Option 1
c. Option 2
d. Summary
4. Adjusting the Benchmark and Average
Per Capita Expenditures for Beneficiary
Characteristics
5. Technical Adjustments to the
Benchmark Impact of IME and DSH
6. Technical Adjustments to the
Benchmark Impact of Geographic
Payment Adjustments on the Calculation
of the Benchmark
7. Technical Adjustments to the
Benchmark Impact of Bonus Payments
and Penalties on the Calculation of the
Benchmark and Actual Expenditures
8. Trending Forward Prior Years’
Experience To Obtain an Initial
Benchmark
a. Flat Dollar vs Growth Rate as a
Benchmark Trending Factor
b. National vs Local Growth Rate as a
Benchmark Trending Factor
9. Updating the Benchmark During the
Agreement Period
10. Minimum Savings Rate (MSR) and
Sharing Rate
11. Net Sharing Rate
12. Additional Shared Savings Payments
13. Withholding Performance Payments To
Offset Future Losses
14. Performance Payment Limit
G. Two-Sided Model
1. Risk-Based Payment Models
2. Two Tracks Provide Incremental
Approach to Incorporating Risk
3. Elements of the Two-Sided Model
a. Beneficiary Notification and Protections
b. Eligibility Requirements
c. Quality Performance Measurement and
Scoring
d. Shared Savings Methodology
(1) Minimum Savings Rate
(2) Additional Shared Savings Payments
(3) Net Sharing Rate
(4) Calculating Sharing in Losses
(5) Maximum Shared Savings and Shared
Loss Caps
e. Ensuring ACO Repayment of Shared
Losses
f. Future Participation of Under-performing
Organizations
g. Public Reporting
h. Impact on States
4. Verification of Savings and Losses
H. Monitoring and Termination of ACOs
1. Monitoring Avoidance of At Risk
Beneficiaries
2. Monitoring Compliance with Quality
Performance Standards
3. Terminating an ACO Agreement
4. Reconsideration Review Process
I. Coordination With Other Agencies
1. Waivers of CMP, Anti Kickback, and
Physician Self Referral Laws
2. IRS Guidance Relating to Tax Exempt
Organization
3. Antitrust Policy Statement
4. Prohibition Against the Shared Savings
Program Participation by ACOs With
Market Power
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a. Coordinating the Shared Savings
Program Application With the Antitrust
Agencies
b. Competition and Quality of Care
c. Competition, Price, and Access to Care
J. Overlap With Other CMS Shared Savings
Initiatives
1. Duplication in Participation in Medicare
Shared Savings Programs
2. Transition of the Physician Group
Practice (PGP) Demonstration Sites Into
the Shared Savings Program
3. Overlap With the Center for Medicare &
Medicaid Innovation (Innovation Center
Shared Savings Models
III. Collection of Information Requirements
IV. Response to Comments
V. Regulatory Impact Analysis
A. Introduction
B. Statement of Need
C. Anticipated Effects
1. Effects on the Medicare Program
a. Assumptions and Uncertainties
b. Detailed Stochastic Modeling Results
c. Further Considerations
2. Impact on Beneficiaries
3. Impact on Providers and Suppliers
D. Alternatives Considered
E. Accounting Statement and Table
F. Conclusion
Acronyms
ACO Accountable Care Organizations
AHRQ Agency for Healthcare Research and
Quality
BCBSMA Blue Cross Blue Shield of
Massachusetts
BIPA Benefits Improvement and Protection
Act
BQI Better Quality Information
CAD Coronary Artery Disease
CAHPS Consumer Assessment of Health
Providers and Systems
CAHs Critical Access Hospitals
CAM Complementary and Alternative
Services
CBIC Competitive Bidding Implementation
Contractor
CCNC Community Care of North Carolina
CHCs Community Health Centers
CHIP Children’s Health Insurance Program
CMMI Center for Medicare and Medicaid
Innovation
CMP Civil Monetary Penalties
CMS Centers for Medicare and Medicaid
Services
CNM Certified Nurse Midwife
CMS–HCC CMS Hierarchal Condition
Category
COPD Chronic Obstructive Pulmonary
Disease
CP Certified Psychologist
CSW Clinical Social Worker
CVE Chartered Value Exchange
CWF Common Working File
DHHS Department of Health and Human
Services
DM Diabetes Mellitus
DOJ Department of Justice
DRA Deficit Reduction Act of 2005(Pub. L.
109–171)
DSH Disproportionate Share Hospital
DUA Data use Agreement
E&M Evaluation and Management
EDB Enrollment Database
EHR Electronic Health Record
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ESRD End Stage Renal Disease
eRx Electronic Prescribing Incentive
Program
FFS Fee For Service
FQHCs Federally Qualified Health Centers
FTC Federal Trade Commission
GAO Government Accountability Office
GPCI Geographic Practice Cost Index
GPRO Group Practice Reporting Option
HAC Hospital Acquired Conditions
HCAHPS Health Care Providers Systems
and Surveys
HCC Hierarchal Condition Category
HCO Health Care Organizations
HCPCS Health Care Procedural Coding
System
HHA Home Health Agencies
HICN Health Insurance Claim Number
HIPAA Heath Insurance Portability and
Accountability Act of 1996
HIE Health Information Exchange
HIT Health Information Technology
HITECH Health Information Technology for
Economic and Clinical Health
HMO Health Maintenance Organization
HRSA Health Resources Services
Administration
HVBP Hospital Value Based Purchasing
IHIE Indiana Health Information Exchange
IME Indirect Medical Education
INPC Indiana Network for Patient Care
IOM Institute of Medicine
IPPS Inpatient Prospective Payment System
IQR Inpatient Quality Reporting
IRS Internal Revenue Services
LTCHs Long-Term Acute Care Hospitals
MA Medicare Advantage
MAeHC Massachusetts eHealth
Collaborative
MDCs Major Diagnostic Categories
MedPAC Medicare Payment Advisory
Commission
MHCQ Medicare Health Care Quality
MMA Medicare Prescription Drug,
Improvement, and Modernization Act
MPFS Medicare Physician Fee Schedule
MS–DRGs Medicare Severity-Diagnosis
Related Groups
MSP Minimum Savings Percentage
MSR Minimum Savings Rate
NC–CCN North Carolina Community Care
Networks
NCH National Claims History
NCQA National Committee for Quality
Assurance
NP Nurse Practitioner
NPI National Provider Identifier
NQF National Quality Forum
NYCLIX The New York Clinical
Information Exchange
OIG Office of Inspector General
OMB Office of Management and Budget
PA Physician Assistant
PACE Program of All Inclusive Care for the
Elderly
PACFs Post-Acute Care Facilities
PCMH Patient Centered Medical Home
PFS Physician Fee Schedule
PGP Physician Group Practice
PHI Protected health information
POS Point of Service
PPO Preferred provider organization
PPS Prospective Payment System
PQRI Physician Quality Reporting Initiative
PQRS Physician Quality Reporting System
PRA Paperwork Reduction Act
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PSA Primary Service Areas
RFI Request for Information
RHCs Rural Health Centers
RHQDAPU Reporting Hospital Quality Data
for Annual Payment Update
RIA Regulatory Impact Analysis
SNFs Skilled Nursing Facilities
SOR Privacy Act Systems of Record
SSA Social Security Administration
SSN Social Security Number
TIN Tax Identification Number
I. Background
A. Introduction and Overview of ValueBased Purchasing
On March 23, 2010, the Patient
Protection and Affordable Care Act
(Pub. L. 111–148) was enacted.
Following the enactment of Public Law
111–148, the Health Care and Education
Reconciliation Act of 2010 (Pub. L. 111–
152) (enacted on March 30, 2010),
amended certain provisions of Public
Law 111–148. These public laws are
collectively known as the Affordable
Care Act. The Affordable Care Act
includes a number of provisions
designed to improve the quality of
Medicare services, support innovation
and the establishment of new payment
models in the program, better align
Medicare payments with provider costs,
strengthen program integrity within
Medicare, and put Medicare on a firmer
financial footing.
With respect to quality improvement,
the Affordable Care Act includes
provisions to expand value-based
purchasing, broaden quality reporting,
improve the level of performance
feedback available to suppliers, create
incentives to enhance quality, improve
beneficiary outcomes, and increase the
value of care.
Value-based purchasing is a concept
that links payment directly to the
quality of care provided and is a strategy
that can help transform the current
payment system by rewarding providers
for delivering high quality, efficient
clinical care. We have significant
experience in developing, refining, and
expanding health care quality
performance measures through our
experience with value-based
demonstration efforts, noting some of
these efforts later in the document, and
various Medicare payment systems. For
example, since 2005, we have applied
the Hospital Inpatient Quality Reporting
(IQR) Program under the hospital
inpatient prospective payment system.
Hospital IQR provides differential
payments to hospitals that meet certain
requirements, including publicly
reporting their performance on a
defined set of inpatient care
performance measures. Beginning in
2007, under the physician fee schedule,
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we have provided for quality measure
reporting through the Physician Quality
Reporting System, which includes
incentive payments for eligible
professionals who satisfactorily report
data on quality measures for covered
professional services furnished to
Medicare beneficiaries. In 2009,
Congress passed the Health Information
and Technology for Economic and
Clinical Health (HITECH) Act. As part of
the Electronic Health Records (EHR)
Incentive Program under HITECH, we
have defined measures for the
meaningful use of certified electronic
health records technology and have
developed incentive payment programs
for both Medicare and Medicaid
providers. We have extended similar
efforts to additional payment systems,
including the hospital outpatient
prospective payment system and
various post-acute care systems.
In addition to improving quality,
value-based purchasing initiatives seek
to reduce growth in health care
expenditures. It is widely recognized
that the trajectory for the nation’s health
care spending is unsustainable.
Medicare beneficiaries share in the
burden of rising costs, as they pay
higher premiums, and larger costsharing obligations and out-of-pocket
expenses. The Affordable Care Act
includes a series of reforms expected to
significantly slow growth in the
Medicare spending rate while
simultaneously strengthening the care
provided to Medicare beneficiaries.
These reforms build upon existing
value-based purchasing efforts currently
underway within CMS to find ways to
better coordinate care and reduce
unnecessary services to lower the
growth in Medicare spending while
improving the quality of care received
by beneficiaries.
We view value-based purchasing as
an important step to revamping how
care and services are paid for, moving
increasingly toward rewarding better
value, outcomes, and innovations
instead of merely volume. In
implementing these value-based
purchasing initiatives, we seek to meet
certain common goals, as follows:
• Improving quality.
++ Value-based payment systems and
public reporting should rely on a mix of
standards, processes, outcomes, and
patient experience measures, including
measures of care transitions and
changes in patient functional status.
Across all programs, we seek to move as
quickly as possible to the use of
outcome and patient experience
measures. To the extent practicable and
appropriate, these outcome and patient
experience measures should be adjusted
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for risk or other appropriate patient,
population, or provider characteristics.
++ To the extent possible, and
recognizing differences in payment
system readiness and statutory
authorities, measures should be aligned
across Medicare and Medicaid’s public
reporting and payment systems. We
seek to evolve a focused core-set of
measures appropriate to each specific
provider category that reflects the level
of care and the most important areas of
service and measures for that provider.
++ The collection of information
should minimize the burden on
providers to the extent possible. As part
of that effort, we will continuously seek
to align our measures with the adoption
of meaningful use standards for health
information technology (HIT), so the
collection of performance information is
part of care delivery.
++ To the extent practicable, the
measures used by the Shared Savings
Program should be nationally endorsed
by a multistakeholder organization. We
should align measures with best
practices among other payers and the
needs of the end users of the measures.
• Lowering growth in expenditures.
++ Providers should be accountable
for the cost of care, and be rewarded for
reducing unnecessary expenditures and
be responsible for excess expenditures.
++ In reducing excess expenditures,
providers should continually improve
the quality of care they deliver and must
honor their commitment to do no harm
to beneficiaries.
++ To the extent possible, and
recognizing differences in payers’ valuebased purchasing initiatives, providers
should apply cost reducing and quality
improving redesigned care processes to
their entire patient population.
As noted previously, the Affordable
Care Act includes provisions to expand
value-based purchasing, broaden quality
reporting, improve the level of
performance feedback available to
suppliers, create incentives to enhance
quality, improve beneficiary outcomes,
and increase the value of care. Among
these provisions, section 3022 of the
Affordable Care Act requires the
Secretary to establish the Medicare
Shared Savings Program (Shared
Savings Program), intended to
encourage the development of
Accountable Care Organizations (ACOs)
in Medicare. The Affordable Care Act
intends the Medicare Shared Saving
Program to be a program ‘‘that promotes
accountability for a patient population
and coordinates items and services
under parts A and B, and encourages
investment in infrastructure and
redesigned care processes for high
quality and efficient service delivery.’’
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The Shared Savings Program is a key
Medicare delivery system reform
initiatives that will be implemented
under the Affordable Care Act and is a
new approach to the delivery of health
care aimed at: (1) Better care for
individuals; (2) better health for
populations; and (3) lower growth in
expenditures. We refer to this approach
throughout the document as the threepart aim.
B. Statutory Basis for the Medicare
Shared Savings Program
Section 3022 of the Affordable Care
Act amended Title XVIII of the Social
Security Act (the Act) (42 U.S.C. 1395
et seq.) by adding new section 1899 to
the Act to establish a Shared Savings
Program that promotes accountability
for a patient population, coordinates
items and services under Parts A and B,
and encourages investment in
infrastructure and redesigned care
processes for high quality and efficient
service delivery. Section 1899(a)(1) of
the Act requires the Secretary to
establish this program no later than
January 1, 2012. Section 1899(a)(1)(A) of
the Act further provides that, ‘‘groups of
providers of services and suppliers
meeting criteria specified by the
Secretary may work together to manage
and coordinate care for Medicare feefor-service beneficiaries through an
[ACO]’’. Section 1899(a)(1)(B) of the Act
also provides that ACOs that meet
quality performance standards
established by the Secretary are eligible
to receive payments for ‘‘shared
savings’’.
Section 1899(b)(1) of the Act
establishes the types of groups of
providers of services and suppliers,
with established mechanisms for shared
governance, that are eligible to
participate as ACOs under the program,
subject to the succeeding provisions of
section 1899 of the Act, as determined
appropriate by the Secretary.
Specifically, sections 1899(b)(1)(A)
through (E) of the Act provide,
respectively, that the following groups
of providers of services and suppliers
are eligible to participate:
• ACO professionals in group practice
arrangements.
• Networks of individual practices of
ACO professionals.
• Partnerships or joint venture
arrangements between hospitals and
ACO professionals.
• Hospitals employing ACO
professionals.
• Such other groups of providers of
services and suppliers as the Secretary
determines appropriate.
Section 1899(b)(2) of the Act
establishes the requirements that such
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eligible groups must meet in order to
participate in the program. Specifically,
sections 1899(b)(2)(A) through (H) of the
Act provide, respectively, that eligible
groups of providers of services and
suppliers must meet the following
requirements to participate in the
program as ACOs:
• The ACO shall be willing to become
accountable for the quality, cost, and
overall care of the Medicare fee-forservice (FFS) beneficiaries assigned to
it.
• The ACO shall enter into an
agreement with the Secretary to
participate in the program for not less
than a 3-year period.
• The ACO shall have a formal legal
structure that would allow the
organization to receive and distribute
payments for shared savings to
participating providers of services and
suppliers.
• The ACO shall include primary care
ACO professionals that are sufficient for
the number of Medicare FFS
beneficiaries assigned to the ACO. At a
minimum, the ACO shall have at least
5,000 such beneficiaries assigned to it in
order to be eligible to participate in the
Shared Savings Program.
• The ACO shall provide the
Secretary with such information
regarding ACO professionals
participating in the ACO as the
Secretary determines necessary to
support the assignment of Medicare feefor-service beneficiaries to an ACO, the
implementation of quality and other
reporting requirements, and the
determination of payments for shared
savings.
• The ACO shall have in place a
leadership and management structure
that includes clinical and administrative
systems.
• The ACO shall define processes to
promote evidence-based medicine and
patient engagement, report on quality
and cost measures, and coordinate care,
such as through the use of telehealth,
remote patient monitoring, and other
such enabling technologies.
• The ACO shall demonstrate to the
Secretary that it meets patientcenteredness criteria specified by the
Secretary, such as the use of patient and
caregiver assessments or the use of
individualized care plans.
Section 1899(b)(3) of the Act
establishes the quality and other
reporting requirements for the Shared
Savings Program. For purposes of
quality reporting, section 1899(b)(3)(A)
of the Act provides that the Secretary
shall determine appropriate measures to
assess the quality of care furnished by
the ACO, such as measures of clinical
processes and outcomes, patient and,
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where practicable, caregiver experience
of care, and utilization (such as rates of
hospital admissions for ambulatory care
sensitive conditions). Section
1899(b)(3)(B) of the Act requires an ACO
to submit data in a form and manner
specified by the Secretary on measures
the Secretary determines necessary for
the ACO to report in order to evaluate
the quality of care furnished by the
ACO. This provision further states that
such data may include care transitions
across health care settings, including
hospital discharge planning and posthospital discharge follow-up by ACO
professionals, as determined to be
appropriate by the Secretary. Section
1899(b)(3)(C) of the Act requires the
Secretary to establish quality
performance standards to assess the
quality of care furnished by ACOs. That
section also requires that the Secretary
shall seek to improve the quality of care
furnished by ACOs over time by
specifying higher standards, new
measures, or both for purposes of
assessing such quality of care. Finally,
section 1899(b)(3)(D) of the Act provides
that the Secretary may, as the Secretary
determines appropriate, incorporate
reporting requirements and incentive
payments related to the Physician
Quality Reporting System under section
1848 of the Act, including such
requirements and such payments related
to electronic prescribing, electronic
health records, and other similar
initiatives under section 1848 of the
Act, and may use alternative criteria
than would otherwise apply under such
section for determining whether to make
such payments. CMS should not take
the incentive payments described in the
preceding sentence into consideration
when calculating any payments
otherwise made under of section
1899(d) the Act.
Section 1899(b)(4) of the Act prohibits
duplication in participation in other
shared savings programs by participants
in the Shared Savings Program.
Specifically, a provider of services or
supplier that participates in any of the
following is not eligible to participate in
an ACO under the Shared Savings
Program: A model tested or expanded
under section 1115A of the Act that
involves shared savings under this title,
any other program or demonstration
project that involves such shared
savings, or the Independence at Home
Demonstration under section 1866E of
the Act.
Section 1899(c) of the Act provides
the Secretary with discretion to
determine an appropriate method to
assign Medicare FFS beneficiaries to an
ACO participating in the Shared Savings
Program. This discretion is limited,
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however, by the fact that under the Act,
assignment must be based on
beneficiaries’ utilization of primary care
services provided under Medicare by an
ACO professional who is a physician as
defined in section 1861(r)(1) of the Act.
Section 1899(d) of the Act establishes
the principles and requirements for
payments and treatment of savings
under the Shared Savings Program.
Specifically, section 1899(d)(1)(A) of the
Act provides that, subject to the
requirements concerning monitoring
avoidance of at-risk patients, payments
shall continue to be made to providers
of services and suppliers participating
in an ACO under the original Medicare
FFS program under Parts A and B in the
same manner as they would otherwise
be made, except that a participating
ACO is eligible to receive payment for
shared savings if the following occur:
• The ACO meets quality
performance standards established by
the Secretary; and
• The ACO meets the requirements
for realizing savings.
Section 1899(d)(1)(B) of the Act
establishes the savings requirements
and the method for establishing and
updating the benchmark against which
any savings would be determined.
Specifically, section 1899(d)(1)(B)(i) of
the Act establishes that, in each year of
the agreement period, an ACO shall be
eligible to receive payment for shared
savings only if the estimated average per
capita Medicare expenditures under the
ACO for Medicare FFS beneficiaries for
Parts A and B services, adjusted for
beneficiary characteristics, is at least the
percent specified by the Secretary below
the applicable benchmark. The
Secretary shall determine the
appropriate percent of shared savings to
account for normal variation in
Medicare expenditures, based upon the
number of Medicare FFS beneficiaries
assigned to an ACO. Section
1899(d)(1)(B)(ii) of the Act, in turn,
requires the Secretary to estimate a
benchmark for each agreement period
for each ACO using the most recent
available 3 years of per beneficiary
expenditures for Parts A and B services
for Medicare FFS beneficiaries assigned
to the ACO. This benchmark must be
adjusted for beneficiary characteristics
and such other factors as the Secretary
determines appropriate and updated by
the projected absolute amount of growth
in national per capita expenditures for
Parts A and B services under the
original Medicare FFS program, as
estimated by the Secretary.
Furthermore, the benchmark must be
reset at the start of each new agreement
period.
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Section 1899(d)(2) of the Act provides
for the actual payments for shared
savings under the Shared Savings
Program. Specifically, if an ACO meets
the quality performance standards
established by the Secretary, and meets
the savings requirements, a percent (as
determined appropriate by the
Secretary) of the difference between the
estimated average per capita Medicare
expenditures in the year, adjusted for
beneficiary characteristics, and the
benchmark for the ACO may be paid to
the ACO as shared savings and the
remainder of the difference shall be
retained by the Medicare program. The
Secretary is required to establish limits
on the total amount of shared savings
paid to an ACO.
Section 1899(d)(3) of the Act requires
the Secretary to monitor ACOs for
avoidance of at-risk patients.
Specifically, if the Secretary determines
that an ACO has taken steps to avoid
patients at risk in order to reduce the
likelihood of increasing costs to the
ACO, the Secretary may impose an
appropriate sanction on the ACO,
including termination from the program.
Section 1899(d)(4) of the Act, in turn,
provides that the Secretary may
terminate an agreement with an ACO if
it does not meet the quality performance
standards established by the Secretary.
Section 1899(e) of the Act provides that
chapter 35 of title 44 of the U.S. Code,
which includes such provisions as the
Paperwork Reduction Act (PRA), shall
not apply to the Shared Savings
Program. Section 1899(f) of the Act
further provides the Secretary with the
authority to waive such requirements of
sections 1128A and 1128B of the Act
and title XVIII of the Act as may be
necessary to carry out the Shared
Savings Program. Section 1899(g) of the
Act establishes limitations on judicial
and administrative review of the Shared
Savings Program. This section provides
that there shall be no administrative or
judicial review under section 1869 of
the Act, section 1878 of the Act, or
otherwise of the following:
• The specification of criteria under
1899(a)(1)(B) of the Act.
• The assessment of the quality of
care furnished by an ACO and the
establishment of performance standards
under 1899(b)(3) of the Act.
• The assignment of Medicare FFS
beneficiaries to an ACO under 1899(c)
of the Act.
• The determination of whether an
ACO is eligible for shared savings under
1899(d)(2) of the Act and the amount of
such shared savings, including the
determination of the estimated average
per capita Medicare expenditures under
the ACO for Medicare FFS beneficiaries
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assigned to the ACO and the average
benchmark for the ACO under
1899(d)(1)(B) of the Act.
• The percent of shared savings
specified by the Secretary under
1899(d)(2) of the Act and any limit on
the total amount of shared savings
established by the Secretary under such
subsection.
• The termination of an ACO under
1899(d)(4) of the Act for failure to meet
the quality performance standards.
Section 1899(h) of the Act defines
some basic terminology that applies to
the Shared Savings Program.
Specifically, section 1899(h)(1) of the
Act defines the term ‘‘ACO professional’’
as a physician (as defined in section
1861(r)(1) of the Act) or a practitioner
described in section 1842(b)(18)(C)(i) of
the Act (that is, a physician assistant,
nurse practitioner or clinical nurse
specialist (as defined in section
1861(aa)(5) of the Act)). Section
1899(h)(2) of the Act defines the term
‘‘hospital’’ as a hospital (as defined in
section 1886(d)(1)(B) of the Act.’’ (A
‘‘subsection (d) hospital’’ is a hospital
located in one of the fifty States or the
District of Columbia, excluding
hospitals and hospital units that are not
paid under the inpatient prospective
payment system under section
1886(d)(1)(B) of the Act, such as
psychiatric, rehabilitation, long term
care, children’s, and cancer hospitals.)
Section 1899(h)(3) of the Act defines the
term ‘‘Medicare fee-for-service
beneficiary’’ as an individual who is
enrolled in the original Medicare FFS
program under Medicare Parts A and B
and is not enrolled in a Medicare
Advantage (MA) plan under Medicare
Part C, an eligible organization under
section 1876 of the Act, or a Program of
All-Inclusive Care for the Elderly
(PACE) under section 1894 of the Act.
Section 1899(i) of the Act provides
that the Secretary may use either a
partial capitation model or other
payment model, rather than the
payment model described in section
1899(d) of the Act, for making payments
under the Shared Savings Program.
Sections 1899(i)(2)(B) and 1899(i)(3)(B)
of the Act require that any such model
maintain budget neutrality. Specifically,
these sections require that any such
model adopted by the Secretary, ‘‘does
not result in spending more for such
ACO for such beneficiaries than would
otherwise be expended for such ACO for
such beneficiaries for such year if the
model were not implemented, as
estimated by the Secretary.’’
Finally, section 1899(k) of the Act
provides for an extension to the
Physician Group Practice (PGP)
demonstration: ‘‘During the period
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beginning on the date of the enactment
of this section and ending on the date
the program is established, the Secretary
may enter into an agreement with an
ACO under the demonstration under
section 1866A, subject to rebasing and
other modifications deemed appropriate
by the Secretary.’’
C. Overview and Intent of the Medicare
Shared Savings Program
The intent of the Shared Savings
Program is to promote accountability for
a population of Medicare beneficiaries,
improve the coordination of FFS items
and services, encourage investment in
infrastructure and redesigned care
processes for high quality and efficient
service delivery, and incent higher
value care. As an incentive to ACOs that
successfully meet quality and savings
requirements, the Medicare Program can
share a percentage of the achieved
savings with the ACO. In order to meet
the intent of the Shared Savings
Program as established by the
Affordable Care Act, we will focus on
achieving, as our highest-level goal, the
three-part aim, which consists of the
following:
• Better care for individuals—as
described by all six dimensions of
quality in the Institute of Medicine
report: Safety, effectiveness, patientcenteredness, timeliness, efficiency, and
equity;
• Better health for populations with
respect to educating beneficiaries about
the upstream causes of ill health—like
poor nutrition, physical inactivity,
substance abuse, economic disparities—
as well as the importance of preventive
services such as annual physicals and
flu shots; and
• Lower growth in expenditures by
eliminating waste and inefficiencies
while not withholding any needed care
that helps beneficiaries.
Under the Shared Savings Program,
ACOs will only share in savings if they
first generate shareable savings and then
meet the quality standards. In the spirit
of the three-part aim and the vision of
always keeping the beneficiary in the
forefront of all decisions, we believe
that an ACO should embrace the
following goals:
• An ACO will put the beneficiary
and family at the center of all its
activities. It will honor individual
preferences, values, backgrounds,
resources, and skills, and it will
thoroughly engage people in shared
decision-making about diagnostic and
therapeutic options.
• An ACO will ensure coordination of
care for beneficiaries regardless of its
time or place. In an ACO, people will
find that they no longer carry the
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burden of ensuring that everyone caring
for them has the information they need.
Beneficiaries will see that organizational
teamwork improves their health care.
• An ACO will attend carefully to
care transitions, especially as
beneficiaries journey from one part of
the care system to another.
• An ACO will manage resources
carefully and respectfully. It will ensure
continual waste reduction, and that
every step in care adds value to the
beneficiary. An ACO will be able to
make investments where investments
count, and move resources to meet
beneficiaries’ needs. Because of its
capabilities with respect to prevention
and anticipation, especially for
chronically ill people, an ACO will be
able to continually reduce its
dependence on inpatient care. Instead,
its patients will more likely be able to
be home, where they often want to be,
and, during a hospital admission, they
receive assurance that their discharges
will be well coordinated, and that they
will not return due to avoidable
complications.
• An ACO will be proactive by
reaching out to patients with reminders
and advice that can help them stay
healthy and let them know when it is
time for a checkup or a test.
• An ACO will collect, evaluate, and
use data on health care processes and
outcomes sufficiently to measure what it
achieves for beneficiaries and
communities over time and use such
data to improve care delivery and
patient outcomes.
• An ACO will be innovative in the
service of the three-part aim of better
care for individuals, better health for
populations, and lower growth in
expenditures. It will draw upon the
best, most advanced models of care,
using modern technologies, including
telehealth and electronic health records,
and other tools to continually reinvent
care in the modern age. It will monitor
and compare its performance to other
ACOs, identify and examine new
processes for care improvement, and
adopt those approaches that are
demonstrated to be effective.
• An ACO will continually invest in
the development and pride of its own
workforce, including affiliated
clinicians. It will maintain and execute
plans for helping build skill, knowledge,
and teamwork.
As proposed in this notice of
proposed rulemaking (NPRM), the
Shared Savings Program encourages
providers of services and suppliers to
form ACOs that seek to achieve a threepart aim of better care for individuals,
better health for populations, and lower
growth in expenditures. The proposed
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rule establishes the requirements for
ACOs to take responsibility for
improving the quality of care they
deliver to a group of Medicare FFS
beneficiaries, while lowering the growth
in costs, in return for a share of the
resulting savings. In addition to
establishing a shared savings model for
rewarding quality and financial
performance, the program also holds
ACOs accountable for excess
expenditures by establishing, as an
option, a two-sided risk model which
requires repayment of losses to us. This
represents a new approach for the
Medicare FFS program, under which
providers have traditionally had little or
no financial incentive to coordinate the
care for their patients or to be
accountable for the total costs and
quality of the care provided.
Since there is little comparative
experience with implementing a Shared
Savings Program and alternative
payment models at the national level,
we sought input on the impact of this
proposed program from a wide range of
external experts, including credentialed
actuaries, clinical managers, and
academic researchers on the potential
impact of the program through, for
example, the White House meeting,
multiple listening sessions, Special
Open Door Forum on ACOs, Workshop
Regarding ACOs with CMS, OIG, and
the Antitrust Agencies, and a Request
For Information. Incorporating their
input, we estimate that up to 5 million
Medicare beneficiaries will receive care
from providers participating in ACOs,
many of which are located in higher
cost areas, and that the program can
have a significant impact on lowering
Medicare expenditure growth.
Furthermore, projections on the initial
impact of the program by the
Congressional Budget Office also
suggest the Shared Savings Program
could result in significant savings to the
Medicare program.
We also believe that the Shared
Savings Program should provide an
entry point for all willing organizations
who wish to move in a direction of
providing value-driven healthcare.
Consequently, in accordance with the
authority granted to the Secretary under
section 1899(i) of the Act, we are
proposing for comment creating and
implementing both a shared savings
model (one-sided model) and a shared
savings/losses model (two-sided model).
Under this proposal, balanced
maximum sharing rates under the two
options to provide greater reward for
ACOs accepting risk while maintaining
an incentive to encourage ACOs not
immediately ready to accept risk to
participate in the one-sided model. This
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approach provides an entry point for
organizations with less experience
managing care and accepting financial
risk, such as physician-driven
organizations or smaller ACOs, to gain
experience with population
management in the FFS setting before
transitioning to more risk.
We believe that ACOs electing to
initially enter the one-sided model
automatically transition to a two-sided
risk model during the final year of their
initial agreement. We also believe that a
two-sided model that builds off a onesided model could be offered as an
option at the beginning of the program.
We would immediately reward ACOs
electing to enter the two-sided model
with higher sharing rates available
under that model. This approach
provides an opportunity for more
experienced ACOs that are ready to
accept risk to enter a sharing
arrangement that provides greater
reward for greater responsibility. For
more detail on the two-sided risk model
refer to section II.G. of this proposed
rule.
In addition to the opportunity to
implement alternative payment models
such as partial capitation under 1899(i)
of the Act, the Center for Medicare and
Medicaid Innovation (Innovation
Center), created by the Affordable Care
Act also has authority to test innovative
payment models. As we gain experience
with the shared savings model and
alternative payment models, we will
continue to refine and improve the
program over time to make it
increasingly effective in achieving our
three-part aim of better care for
individuals, better health for
populations, and lower growth in
expenditures. Finally, in developing the
Shared Savings Program, and in
response to stakeholder suggestions, we
have worked very closely with agencies
across the Federal government to
develop policies to encourage
participation and to ensure a
coordinated and aligned inter- and
intra-agency effort in the
implementation of the program. The
result of this effort is the release of
several notices with which potential
participants are strongly encouraged to
become familiar. Detailed descriptions
of these notices appear in section II.I of
this proposed rule, and include: (1) A
joint CMS and DHHS OIG Medicare
Program; Waiver Designs in Connection
with the Medicare Shared Savings
Program and the Innovation Center;
(2) an Internal Revenue Service (IRS)
notice soliciting comments regarding
the need for additional tax guidance for
tax-exempt organizations, including taxexempt hospitals, participating in the
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Shared Savings Program; and (3) a
proposed Antitrust Policy Statement
issued by the FTC and DOJ (collectively,
the Antitrust Agencies).
D. Related Affordable Care Act
Provisions
The Affordable Care Act intends to
improve quality and make health care
more affordable through the Shared
Savings Program as well as through
other provisions. There are four
programs authorized by the Affordable
Care Act discussed later in the
document which may affect Shared
Savings Program policy or help to guide
future Shared Savings Program policy,
or may intersect with the Shared
Savings Program in other ways.
1. Establishment of Center for Medicare
and Medicaid Innovation (Innovation
Center)
Section 1115A of the Act, as added by
section 3021 of the Affordable Care Act,
required the establishment of the new
Innovation Center not later than January
1, 2011 to test innovative payment and
service delivery models to reduce
program expenditures under Medicare,
Medicaid, and the Children’s Health
Insurance Program (CHIP) while
preserving or enhancing the quality of
care furnished to beneficiaries under
these programs. In selecting such
models for testing, the statute requires
the Secretary to give preference to
models that also improve the
coordination, quality, and efficiency of
health care services furnished under
Medicare, Medicaid, and CHIP.
Section 1115A authorizes the
Secretary to expand the duration and
scope of a model being tested through
rulemaking (including implementation
on a nationwide basis) to the extent the
Secretary—
• Determines expected expansion to
reduce spending under the applicable
title without reducing the quality of care
or improve the quality of patient care
without increasing spending;
• Obtains a certification from our
Chief Actuary that such expansion
would reduce (or would not result in
any increase in) net program spending
under applicable titles; and
• Determines that such expansion
would not deny or limit the coverage or
provision of benefits under Medicare,
Medicaid, or CHIP.
Through the Innovation Center, we
plan to explore alternative payment
models for the Shared Savings Program.
As we test and refine these models, gain
operational experience, and put the
necessary infrastructure in place to
support program wide implementation,
including critical monitoring and
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patient protection infrastructure, we
plan to make these options available
under the Shared Savings Program in
future rulemaking. Our intent is to move
participants of the demonstration
models that have a demonstrated track
record of realizing shared savings and
high quality performance into the
Shared Savings Program in future
agreement periods.
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2. Independence at Home Medical
Practices
Section 1866E of the Act, as added by
section 3024 of the Affordable Care Act
authorizes the Secretary to conduct a
demonstration program to test a
payment incentive and service delivery
model that utilizes Independence at
Home Medical Practices, which are
comprised of physician and nurse
practitioner directed home-based
primary care teams, to provide services
designed to reduce expenditures and
improve health outcomes for certain
Medicare beneficiaries.
Subject to performance on quality
measures established for the
demonstration, participating practices
may be eligible to receive an incentive
payment in the form of shared savings.
In determining whether savings were
generated, the Secretary shall establish
an estimated annual spending target, for
the amount the Secretary estimates
would have been spent in absence of the
demonstration, for items and services
covered under Parts A and B furnished
to applicable beneficiaries for each
qualifying Independence at Home
medical practice. A practice is eligible
to receive an incentive payment if actual
expenditures for the year for the
applicable beneficiaries it enrolls are
less than the estimated spending target
established for the year. An incentive
payment for each year shall be equal to
a portion of the amount by which actual
expenditures for applicable
beneficiaries under Parts A and B for the
year are estimated to be less than 5
percent less than the estimated
spending target for the year.
3. State Option To Provide Health
Homes
Section 1945 of the Act, as added by
section 2703 of the Affordable Care Act
authorizes a State option under
Medicaid to provide a health home for
individuals with chronic conditions.
The definition of the term ‘‘health
home’’ is defined as a designated
provider (including a provider that
operates in coordination with a team of
health care professionals) or a health
team selected by an eligible individual
with chronic conditions to provide
health home services. Health home
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services are defined as comprehensive
and timely high-quality services,
including comprehensive care
management; care coordination and
health promotion; comprehensive
transitional care, including appropriate
follow-up, from inpatient to other
settings; patient and family support
(including authorized representatives);
referral to community and social
support services, if relevant; and use of
health information technology to link
services, as feasible and appropriate.
Under section 1945 of the Act, States
pay the designated provider, team of
health care professionals operating with
such a provider, or health team for the
provision of health home services to
each eligible individual with chronic
conditions that selects them as their
health home. A State specifies in their
State plan amendment the methodology
it will use to determine payment for
health home services. The methodology
may be tiered to reflect, with respect to
each eligible individual with chronic
conditions, the severity or number of
such individual’s chronic conditions or
the specific capabilities of the provider,
team of health care professionals, or
health team. A time-limited higher
Federal Medicaid matching payment is
available for health home services.
4. Community Health Teams
Section 3502 of the Affordable Care
Act requires the Secretary to establish a
program to provide grants to or enter
into contracts with eligible entities to
establish community based
interdisciplinary, inter-professional
teams (referred to in the statute as
‘‘health teams’’) to support primary care
practices, including obstetrics and
gynecology practices, within the
hospital service areas served by the
eligible entities. These grants or
contracts shall be used to establish
health teams to provide support services
to primary care providers and provide
capitated payments to primary care
providers as determined by the
Secretary. For purposes of this section,
primary care is the provision of
integrated, accessible health care
services by clinicians who are
accountable for addressing a large
majority of personal health care needs,
developing a sustained partnership with
patients, and practicing in the context of
the family and community.
A health team established under a
grant or contract must establish
contractual agreements with primary
care providers to provide support
services. The team must support
patient-centered medical homes,
defined as a mode of care that
includes—(1) Personal physicians;
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(2) whole person orientation;
(3) coordinated and integrated care;
(4) safe and high-quality care through
evidence-informed medicine,
appropriate use of health information
technology, and continuous quality
improvements; (5) expanded access to
care; and
(6) payment that recognizes added value
from additional components of patient
centered care.
Health teams must also collaborate
with local primary care providers and
existing State and community-based
resources to coordinate—(1) disease
prevention; (2) chronic disease
management; (3) transitioning between
health care providers and settings; and
(4) case management for patients,
including children, with priority given
to those amenable to prevention and
with chronic diseases or conditions
identified by the Secretary. In
collaboration with local health care
providers, a health team must develop
and implement interdisciplinary,
interprofessional care plans that
integrate clinical and community
preventive and health promotion
services for patients, including children,
with a priority given to those amenable
to prevention and with chronic diseases
or conditions identified by the
Secretary.
E. Related Ongoing CMS Efforts
1. Physician Group Practice
Demonstration
We have previous experience
developing and implementing shared
savings models through demonstrations.
First, under section 412 of the Medicare,
Medicaid, and CHIP Benefits
Improvement and Protection Act of
2000 (BIPA), we implemented the
Physician Group Practice (PGP)
Demonstration in April of 2005—our
first attempt at establishing a Shared
Savings ACO model. The PGP
Demonstration offered a unique
payment model by which PGP providers
received their normal Parts A and B FFS
payments for services rendered and
offered an additional performance
payment for demonstrating ‘‘value.’’ The
performance payments were tied
directly to achieving targets for process
and outcome quality measures as well
as cost savings. The PGP Demonstration
showed that physician-driven
organizations are willing to engage in
efforts to improve the overall quality
and cost efficiency of care for the
patient population they serve. Under the
demonstration, the PGPs were
accountable for a patient population to
whom they provided the plurality of
office-based evaluation and
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management care. The assignment of
patients to the PGP at the end of each
performance year and data has shown
that assigned patients had on average
four or five visits at the PGP during the
year. This provided the opportunity for
the organizations to better coordinate
services and improve the quality and
efficiency of care provided to Medicare
FFS patients. Medicare patients retained
their entitlement to see any Medicare
provider they chose and were not
enrolled or required to only see PGP
physicians under the demonstration.
Based on their experience with the
PGP demonstration, participants
identified several factors as critical to
improving quality and the opportunity
to share savings:
• An integrated organization with an
environment that supports expending
resources on multiple programs and
initiatives to improve quality and
reduce unnecessary services.
• Dedicated physician leadership
with a proven ability to motivate
physicians to participate in the
development and implementation of
quality improvement and other clinical
programs and initiatives.
• Health information technology that
facilitates the aggregation and analysis
of data, allows patient-level feedback,
and provides alerts and reminders at the
point of care.
• Experience with non-Medicare
payer initiatives, particularly through a
managed care affiliate, to improve
quality and reduce expenditure growth.
Under the demonstration, at the end
of the third performance year, all 10 of
the PGPs continued to improve the
quality of care for patients with chronic
illness or who required preventive care
by achieving benchmark or target
performance on at least 28 out of 32
quality markers for patients with
diabetes, coronary artery disease,
congestive heart failure, hypertension,
and for cancer screening. Two of the
PGPs achieved benchmark quality
performance on all 32 quality measures.
Over the course of the first three years,
6 of the 10 groups shared in
approximately $46 million in savings.
2. Medicare Health Care Quality
Demonstration
We have begun testing models under
the Medicare Health Care Quality
(MHCQ) Demonstration, created by the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA) (Pub. L. 108–173). Section
1866C(b) of the Act, as added by section
646 of the MMA, required the Secretary
to establish a 5-year demonstration
program under which the Secretary was
required to approve demonstration
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projects that examine health delivery
factors that encourage the delivery of
improved quality in patient care.
Section 3021(c) of the Affordable Care
Act amended section 1866C of the Act
to allow the Secretary to expand,
through rulemaking, the duration and
scope of a demonstration the Secretary
is conducting under that section to the
extent determined appropriate by the
Secretary if the demonstration meets
certain criteria. The MHCQ
Demonstration Projects design examine
the extent to which major, multi-faceted
changes to traditional Medicare’s health
delivery and financing systems lead to
improvements in the quality of care
provided to Medicare beneficiaries,
without increasing total program
expenditures. We approved one such
program, the Indiana Health Information
Exchange (IHIE).
Beginning July 1, 2009, we began the
first MHQC project, the IHIE’s
implementation of a regional, multipayer, pay-for-performance and quality
reporting program, based (by-and-large)
on a common set of quality measures.
The expectation is such that the IHIE’s
interventions provide important
empirical evidence on the effectiveness
of pay-for-performance, health IT, and
multipayer initiatives in improving the
quality and efficiency of care provided
to Medicare beneficiaries.
IHIE aggregates our claims and
administrative data in the
demonstration with other data
processed in conjunction with its
regional health information exchange
(HIE). Data used from the various
sources generate patient-level and
provider level quality reports, alerts,
and reminders for participating
providers. By incorporating our data
into IHIE’s HIE and producing these
quality reports, IHIE can provide
participating physicians with a more
complete picture of the care that is or is
not being provided to their Medicare
patients and give physicians the
information they need to positively
impact the quality and cost of care being
provided.
During the demonstration, we review
cost and quality data for Medicare FFS
beneficiaries that have at least one office
or other outpatient evaluation and
management (E&M) visit with an IHIE
participating physician. It is expected
that an estimated 100,000 Medicare
beneficiaries residing in the
Indianapolis metropolitan area will
meet this criterion in each year of the
demonstration.
Quality of care is measured at the
population-level (that is, performance
measurement will focus on whether or
not the site has achieved improvements
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in quality when looking at the entire
group of treated patients) using a set of
Medicare specific quality measures.
Improvements in the quality of care
provided to Medicare beneficiaries are
determined on the extent to which IHIE
participating physicians are able to
reduce the gap between the maximum
attainable level for a quality measure
and the baseline performance for the
quality measure. We used
approximately 14 ambulatory care
quality measures in the first year,
growing to approximately 30 in the fifth
year.
Quality-contingent shared savings are
available with our calculating savings in
the intervention population by
comparing actual costs to expected costs
for treated beneficiaries. Expected costs
for the intervention group are projected
using adjusted utilization trends from a
comparison group. In general,
calculated Medicare savings are the
difference between the expected costs
and actual costs for beneficiaries in the
intervention group. At least 50 percent
of shared savings that are available to be
paid for payment to the site are
contingent on quality of care results for
the year. Only after quality of care
performance results for a year are
determined can the final amount of
shared savings to be paid to the site be
determined.
II. Provisions of the Proposed Rule
A. Organization of the Proposed Rule
The remainder of this document is
organized as follows: In section II.A. of
this proposed rule, we propose an
operational definition of an ACO for
purposes of the shared savings program.
In section II.B. of this proposed rule, we
put forth proposed eligibility
requirements for an ACO to participate
in this program. In section II.C. of this
proposed rule, we propose requirements
for an ACO to commit to a 3-year
participation agreement under this
program and present a proposal for data
sharing with ACOs. In section II.D. of
this proposed rule, we discuss our
proposed methodology for assigning
beneficiaries to an ACO. In section II.E.
of this proposed rule, we present our
proposals regarding quality measures
and the methodology for measuring
ACO performance under this program.
In section II.F. of this proposed rule, we
discuss our proposed shared savings
payment methodology, including the
establishment of an expenditure
benchmark, performance target,
minimum savings percentage, sharing
rate, performance cap. In section II.G. of
this proposed rule, we discuss our
proposal for introducing risk into the
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shared savings program, the two-sided
model and differences from the onesided model. In section II.H. of this
proposed rule, we discuss our proposal
for monitoring ACO performance and
we propose grounds and procedures for
terminating agreements. In section II.I.
of this proposed rule, we discuss our
efforts to coordinate the development of
this proposed rule with other Federal
agencies to ensure a coordinated and
aligned inter- and intra-agency effort in
the implementation of the program. In
section II.J. of this proposed rule, we
discuss overlap in Medicare programs
and how this might affect Shared
Savings Program participants. Finally,
in section V. of this proposed rule, we
present our Regulatory Impact Analysis,
which sets forth an analysis of the
impact of these proposals on affected
entities and beneficiaries.
For purposes of this proposed rule,
we propose definitions for the following
terms:
• Accountable care organization
(ACO) means a legal entity that is
recognized and authorized under
applicable State law, as identified by a
Taxpayer Identification Number (TIN),
and comprised of an eligible group (as
discussed in section II.B. of this
proposed rule) of ACO participants that
work together to manage and coordinate
care for Medicare FFS beneficiaries and
have established a mechanism for
shared governance that provides all
ACO participants with an appropriate
proportionate control over the ACO’s
decision making process,
• ACO participant means a Medicareenrolled provider of services and/or a
supplier (as discussed in section II.B. of
this proposed rule, as identified by a
TIN).
• ACO provider/supplier means a
provider of services and/or a supplier
(as discussed in section II.B. of this
proposed rule) that bills for items and
services it furnishes to Medicare
beneficiaries under a Medicare billing
number assigned to the TIN of an ACO
participant in accordance with
applicable Medicare rules and
regulations.
B. Eligibility and Governance
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1. Eligible Entities
Section 1899(b) of the Act establishes
eligibility requirements for ACOs
participating in the Shared Savings
Program. Section 1899(b)(1) of the Act
allows several designated groups of
providers of services and suppliers to
participate as an ACO under this
program, ‘‘as determined appropriate by
the Secretary,’’ and under the condition
that they have ‘‘established a mechanism
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for shared governance.’’ The statute lists
the following groups of providers of
services and suppliers as eligible to
participate as an ACO:
• ACO professionals in group practice
arrangements.
• Networks of individual practices of
ACO professionals.
• Partnerships or joint venture
arrangements between hospitals and
ACO professionals.
• Hospitals employing ACO
professionals.
• Such other groups of providers of
services and suppliers as the Secretary
determines appropriate.
Section 1899(h)(1) of the Act defines
an ‘‘ACO professional’’ as a physician (as
defined in section 1861(r)(1) of the Act,
which refers to a doctor of medicine or
osteopathy), or a practitioner (as defined
in section 1842(b)(18)(C)(i) of the Act,
which includes physician assistants,
nurse practitioners, and clinical nurse
specialists). Section 1899(h)(2) of the
Act also provides that, for purposes of
the Shared Savings Program, the term
‘‘hospital’’ means a subsection (d)
hospital as defined in section
1886(d)(1)(B) of the Act, thus limiting
the definition to include only acute care
hospitals paid under the hospital
inpatient prospective payment system
(IPPS). Other providers of services and
suppliers that play a critical role in the
nation’s health care delivery system,
such as Federally qualified health
centers (FQHCs), rural health centers
(RHCs), skilled nursing facilities (SNFs),
nursing homes, long-term care hospitals
(LTCHs) and critical access hospitals
(CAHs), among others, are not
specifically designated as eligible
participants in the Shared Savings
Program under section 1899(b)(1) of the
Act. We note, however, that the
statutorily defined groups of providers
and suppliers that are eligible to
participate in the Shared Savings
Program as ACOs, would also have to
meet the eligibility criteria discussed in
detail later in this proposed rule in
order to qualify for participation in the
program. While the statute enumerates
certain kinds of provider and supplier
groups that are eligible to participate in
this program, it also provides the
Secretary with discretion to tailor
eligibility in a way that narrows or
expands the statutory list of eligible
ACO participants. Therefore, we have
considered whether it would be
advisable, at least in the initial stage of
the Shared Savings Program, to—(1)
Permit participation in the program by
only those ACO participants that are
specifically identified in the statute; (2)
restrict eligibility to those ACO
participants that would most effectively
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advance the goals of the program; or (3)
employ the discretion provided to the
Secretary under section 1899(b)(1)(E) of
the Act to expand the list of eligible
groups to include other types of
Medicare-enrolled providers and
suppliers identified in the Act.
Some have argued that ACOs would
be most effective if they include certain
entities as ACO participants. For
example, the Medicare Payment
Advisory Commission (MedPAC) has
noted that provider groups with
hospitals in their systems may be most
effective in generating savings. The
MedPAC notes that hospitals working
with physician teams can prevent
further hospitalizations after discharge
and provide ongoing services to keep
the patient as healthy as possible. Also,
the savings generated by ACOs, in many
cases, are expected to result from
reduced inpatient admissions. As a
result, provider groups with hospitals
may have a greater incentive to
coordinate care to ensure that a portion
of the revenue lost from decreased
admissions is made up through shared
savings. (To view the MedPAC
discussion referenced previously go to:
https://www.medpac.gov/documents/
jun09_entirereport.pdf.)
Another option for limiting eligibility
would be to restrict eligibility to only
those ACO professionals providing
primary care services. Primary care
professionals may have the best
opportunity to reduce unnecessary costs
by ensuring care coordination for
beneficiaries with multiple chronic
conditions. By coordinating with
specialists to whom the beneficiary has
been referred, primary care providers
can reduce unnecessary repetition of
laboratory testing or imaging. By
ensuring timely access to the outpatient
services, primary care providers can
also reduce the number of avoidable
admissions. Limiting eligibility for the
Shared Savings Program to primary care
providers, therefore, may be desirable to
emphasize the important role played by
these professionals and ensure a
primary care focus for the program.
Adopting either of these approaches
would require a narrower eligibility
definition than is permitted (although
not required) under the statute.
However, the benefits of limiting
eligibility need to be balanced against
the prospect that such limitations could
compromise potential innovations and
forfeit the opportunity to assess new
models that could potentially transform
health care in ways that improve quality
and beneficiary satisfaction while better
controlling costs. More importantly,
defining eligibility narrowly also has the
potential to impede development of
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ACOs that include other provider and
supplier types, especially those that
provide services in rural and other
underserved areas. For example, while
section 1899(b)(1) of the Act does not
mention certain entities such as critical
access hospital (CAHs), federally
qualified health centers (FQHCs), or
rural health clinics (RHCs) in its listing
of entities eligible to form an ACO
under the Shared Savings Program these
entities play a critical role in the
nation’s health care delivery system,
serving as safety net providers of
primary care and other health care and
social services in rural and other
underserved areas and for low-income
beneficiaries, including those dually
eligible for Medicare and Medicaid.
Permitting participation by these groups
of providers and suppliers has the
potential to improve coordination and
quality of care for a greater number of
beneficiaries in more communities,
while better controlling costs in more
varied settings and across a broader
array of providers and suppliers.
Since the statute requires that
beneficiary assignment be determined
on the basis of utilization of primary
care services provided by ACO
professionals that are physicians, we
considered whether expansion of
eligibility would allow additional
Medicare enrolled providers and
suppliers to form an ACO to participate
in addition to the four groups specified
in section 1899(b)(1)(A)–(D) of the Act.
Specifically, we considered whether it
would be feasible for CAHs, FQHCs, and
RHCs to form an ACO or whether it
would be necessary for these entities to
join with the four groups specified in
section 1899(b)(1)(A)–(D) of the Act in
order to meet statutory criteria. We have
especially considered the circumstances
of CAHs, FQHCs, and RHCs because
these entities play a critical role in the
nation’s health care delivery system,
serving as safety net providers of
primary care and other health care and
social services. At the same time, the
specific payment methodologies, claims
billing systems, and data reporting
requirements that apply to these entities
pose some challenges in relation to their
independent participation in the Shared
Savings Program. In order for an entity
to be able to form an ACO, it is
necessary that we obtain sufficient data
in order to carry out the necessary
functions of the program, including
assignment of beneficiaries,
establishment and updating of
benchmarks, and determination of
shared savings, if any. As we discuss in
section II.D of this proposed rule,
consistent with section 1899(c) of the
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Act, which provides that beneficiaries
shall be assigned to an ACO based on
their utilization of primary care services
furnished by an ACO professional who
is a physician, our proposed
methodology for assignment of
beneficiaries is to assign beneficiaries to
an ACO on the basis of receiving a
plurality of their primary care services
as described in section II.D. of this
proposed rule from a physician, as
defined in section 1861(r)(1) of the Act,
with a specialty designation of general
practice, family practice, internal
medicine and geriatric medicine. Thus,
as required by the statute, the
assignment methodology requires data
that identify the precise services
rendered (that is, primary care HCPCS
codes), type of practitioner providing
the service (that is, a MD/DO as opposed
to NP, PA, or clinical nurse specialist),
and the physician specialty in order to
be able to assign beneficiaries to ACOs.
At this time, FQHC claims for services
furnished prior to January 1, 2011 do
not include HCPCS codes that identify
the specific service provided. Thus,
although the claims do contain
information concerning the attending
physician and the rendering health
professional (for example, physician,
physician assistant, nurse practitioner),
who actually provided the service, they
do not currently provide for associating
the rendering provider with the specific
services furnished to the beneficiary.
RHCs predominantly provide primary
care services to their populations. Most
RHC services are provided by nonphysician practitioners such as PAs and
NPs. RHCs submit claims for each
encounter with a beneficiary and
receive payment based on an interim
all-inclusive rate for the RHC. As in the
case of FQHCs, RHC claims distinguish
general classes of services (for example,
clinic visit, home visit by RHC
practitioner, mental health services) by
revenue code, the beneficiary to whom
the service was provided, and other
information relevant to determining
whether the all-inclusive rate can be
paid for the service. These claims do not
include HCPCS codes that identify the
specific service provided. The claims
also contain limited information
concerning the individual practitioner,
or even the type of health professional
(for example, physician, PA, NP), who
provided the service.
For FQHCs and RHCs, therefore, we
currently lack the requisite data
elements (service code, physician,
physician specialty, and specific
attribution of services to the rendering
health care professionals) in the claims
and payment systems to enable us to
determine (1) beneficiary assignment
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during the performance year under
section 1899(c) of the Act, which
requires that assignment to an ACO be
based on utilization of primary care
services furnished by a physician; and
(2) expenditures during the 3-year
benchmark. In the case of FQHCs, we
recently finalized regulations requiring
the collection of HCPCS codes for
services beginning in 2011, in
preparation for the development of the
FQHC PPS. However, there is no
statutory requirement for collecting
from FQHCs the other data elements,
such as the direct link between provider
and service, which would be required
for beneficiary assignment under the
Shared Savings Program. Moreover,
there is neither the statutory
requirement for collection of HCPCS
codes from RHCs nor any plan to
expand this data collection effort to
RHCs. In both the case of FQHCs and
RHCs, reporting the information
necessary to participate in the Shared
Savings Program would be a significant
change in operations that we are
reluctant to impose through regulation
without either a statutory requirement
or clear support for such a regulatory
change from the FQHC and RHC
community at large that they would be
willing to have all RHC/FQHCs provide
this information uniformly, solely to
enable independent formation of an
ACO for purposes of participation in the
Shared Savings Program by the subset of
those FQHC/RHCs that choose to do so.
Therefore, in the absence of the data
elements required for assignment of
beneficiaries, it is not possible for
FQHCs and RHCs to participate in the
Shared Savings Program by forming
their own ACOs. It is, however, possible
for them to join as an ACO participant
in an ACO containing one or more of the
statutory organizations eligible to form
an ACO (as specified in section
1899(b)(1)(A)–(D) of the Act) and upon
which assignment can be made
consistent with the statute and the
assignment methodology proposed in
section II.D. of this proposed rule.
However, we note that even in this case,
for the reasons stated previously, we
would not have the data necessary to
consider FQHC or RHC patients in the
assignment process. Thus, assignment of
beneficiaries to ACOs in which FQHCs
and RHCs are participating would have
to be based solely on data from the other
eligible ACO participants upon whom
assignment can be based. As the Shared
Savings Program develops, we will
continue to assess the possibilities for
collecting the requisite data from
FQHCs and RHCs, and in light of any
such developments we will consider
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whether it is possible at some future
date for Medicare beneficiaries to be
assigned to an ACO on the basis of
services furnished by an FQHC or RHC,
thereby allowing these entities to have
their Medicare beneficiaries included in
the ACO’s assigned population.
The situation is somewhat more
complicated with regard to CAHs.
Section 1834(g) of the Act provides for
two payment methods for outpatient
CAH services.
Under the method specified in section
1834(g)(1) of the Act (referred to as the
standard method), facility services are
paid at 101 percent of reasonable costs
to the CAH through the Medicare fiscal
intermediary or the Medicare Part A/B
MAC, while payments for physician and
other professional services are made
separately to the physician or other
practitioner under the MPFS through
Medicare carriers. Accordingly, CAHs
that bill under the standard method
would not submit claims with
information on individual practitioners,
or the type of health professional (for
example, physician, PA, NP), that
provided a specific service.
Under the method specified in section
1834(g)(2) of the Act (referred to as
method II), a CAH submits bills for both
the facility and the professional services
to its Medicare fiscal intermediary or its
Medicare Part A/B MAC. If a CAH
chooses this method for outpatient
services, the physician or other
practitioner must reassign his or her
right to bill the Medicare program for
those services to the CAH. Under
method II, the CAH receives—(1) 101
percent of the reasonable cost payment
for its facility costs; and (2) 115 percent
of the amount otherwise paid under the
MPFS for professional services under
Medicare.
Thus, current Medicare payment and
billing policies could generally support
the formation of an ACO by a CAH
billing under method II.
In summary, in this proposed rule, we
considered three options for defining
the range of potentially eligible
providers and suppliers that would be
eligible to form an ACO. One option that
we considered would be to limit
eligibility initially to the groups
specifically identified in the statute.
Under this option, only the four groups
specified in section 1899(b)(1)(A)–(D) of
the Act would be eligible to form an
ACO and participate in the program.
A second option would be to
narrowly define which groups of
providers of services and suppliers are
eligible to form an ACO and participate
in the Shared Savings Program. The
approach noted by MedPAC is one
example of this option. This option
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would require the participation of a
hospital in the ACO so that only
partnerships or joint venture
arrangements between hospitals and
ACO professionals or hospitals
employing ACO professionals (groups
specified in 1899(b)(1)(C)–(D) of the
Act) would be eligible to participate in
the program. Another example of this
option would be limiting participation
to only those entities comprised of
primary care professionals so that only
ACO professionals in group practice
arrangements or networks of individual
practices of ACO professionals (groups
specified in 1899(b)(1)(A)–(B) of the
Act) would be eligible to form an ACO
and participate in the program. This
approach would be grounded in the
premise that ACOs should be primary
care-focused and that primary care
professionals are in the best position to
both reduce the fragmentation of
services and improve the overall quality
of care delivered to Medicare
beneficiaries.
Under the third option, the four
groups specified in section
1899(b)(1)(A)–(D) of the Act would be
eligible to form an ACO and participate
in the program, but in addition, we
would employ the discretion provided
to the Secretary under section
1899(b)(1)(E) of the Act to allow other
Medicare enrolled entities, such as
CAHs billing under method II to form an
ACO. Additionally, employing
Secretarial discretion to expand the
definition of eligible providers or
suppliers would allow other Medicare
enrolled entities such as FQHCs and
RHCs, to become ACO participants, if
the ACO that is formed is able to meet
the other qualifications to participate in
the program.
After evaluating the three options for
defining the range of potentially eligible
providers and suppliers, we have
decided to propose the third option.
Under this proposal, the four groups
specifically identified in section
1899(b)(1)(A)–(D) of the Act, and CAHs
billing under method II, would have the
opportunity to form ACOs
independently. In addition, the four
statutorily indentified groups, as well as
CAHs billing under method II, could
establish an ACO with broader
collaborations by including additional
Medicare enrolled entities such as
FQHCs and RHCs and other Medicareenrolled providers and suppliers as
defined in the Act as ACO participants.
While this proposal potentially
increases the administrative complexity
of implementing the program and could
also require stronger measures to
oversee the varied kinds of ACO
arrangements that might evolve, we
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believe this approach best serves the
goals of the program by allowing greater
opportunities for broadly transforming
the health care delivery system and
increasing access to high quality and
lower cost care under the Shared
Savings Program for Medicare
beneficiaries regardless of where they
live. Specifically, this option allows for
a wide variety of ACO configurations
that incorporate a broad range of health
care providers and suppliers, including
safety net providers, post-acute care
facilities, FQHCs, RHCs, and CAHs,
which we believe will enable ACOs to
offer more comprehensive care and
better serve the needs of rural
communities. The proposal also offers
greater opportunity for innovation by
ACOs in determining the most effective
organizational structure to meet the
needs of their respective populations.
In addition to requesting comment on
this proposal generally, we are soliciting
comment on the following: (1) The
kinds of providers and suppliers that
should or should not be included as
potential ACO participants; (2) the
potential benefits or concerns regarding
including or not including certain
provider or supplier types; (3) the
administrative measures that would be
needed to effectively implement and
monitor particular partnerships; (4)
other ways in which we could employ
the discretion provided to the Secretary
to allow the independent participation
of providers and suppliers not
specifically mentioned in the statute, for
example, through an ACO formed by a
group of FQHCs and RHCs; and (5) any
operational issues associated with our
proposal. We will consider whether it
would be appropriate to expand the list
of entities eligible to participate in the
Shared Savings Program, either in the
final rule or in future rulemaking, if we
determine that it is feasible and
consistent with the requirements of the
program for more entities to participate
as ACOs. In the interim, and until such
time as FQHCs and RHCs would be
eligible to form ACOs or have their
patients assigned to an ACO, we are also
proposing to provide an incentive for
ACOs to include RHCs and FQHCs as
ACO participants, by allowing ACOs
that include such entities to receive a
higher percentage of any shared savings
under the program. We believe that this
proposal to encourage participation by
RHCs and FQHCs in ACOs is
appropriate in light of the special role
that these entities play in the health care
delivery system, especially in providing
care to otherwise underserved and
vulnerable populations. We discuss how
this proposal affects the determination
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of shared savings under the program in
section II.F. of this proposed rule.
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2. Legal Structure and Governance
Section 1899(b)(2)(C) of the Act
requires an ACO to ‘‘have a formal legal
structure that would allow the
organization to receive and distribute
payments for shared savings’’ to
‘‘participating providers of services and
suppliers.’’ As previously noted, section
1899(b)(1) of the Act also requires ACO
participants to have a ‘‘mechanism for
shared governance’’ in order to
participate in the program.
Operationally, an ACO’s legal structure
must provide both the basis for its
shared governance as well as the
mechanism for it to receive and
distribute shared savings payments to
ACO participants and providers/
suppliers.
a. Legal Entity
The ACO’s legal entity may be
structured in a variety of ways,
including as a corporation, partnership,
limited liability company, foundation,
or other entity permitted by State law.
As discussed previously in section II. B.
of this proposed rule, and consistent
with section 1899(b)(1)(A)–(D) of the
Act, certain specified groups of
providers of services and suppliers who
have a mechanism of shared governance
may be eligible to participate as ACOs
in the Shared Savings Program. In
addition to the groups specifically
identified in the statute, we are
proposing to use the Secretary’s
discretion under section 1899(b)(1)(E) of
the Act to expand the list of eligible
groups of providers and suppliers that
may participate in the Shared Savings
rogram. Specifically, we are proposing
that ACOs may incorporate other groups
of Medicare enrolled providers and
suppliers, many of whom would not be
able to form ACOs and participate in the
program independently. As described
previously, each of the Medicareenrolled providers and suppliers that
join together to form an ACO is
identified by their Medicare-enrolled
TIN and is referred to herein as an ACO
participant. Regardless of whether an
ACO participant is able to meet the
eligibility criteria for participation in
the Shared Savings Program
independently or must join with others
in order to meet criteria, we propose
that the ACO must demonstrate a
mechanism of shared governance that
provides all ACO participants with an
appropriate proportionate control over
the ACO’s decision making process.
In response to the request for
information (RFI) that appeared in the
November 17, 2010 Federal Register (75
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FR 70165), we received comments
regarding the need for us to remain
flexible when defining the required
legal structure to allow for a variety of
structural options. For example,
commenters noted that we should
permit existing organizations to
participate in the Shared Savings
Program instead of requiring the
formation of a new legal entity in order
to avoid additional costs and
duplication of organizational
competencies. Commenters also
recommended that the legal structure
requirements should not disadvantage
solo and small groups of physicians
with fewer resources relative to larger
hospital and physician groups by
requiring the use of specific structures
that may result in increased costs,
implementation delays, and
cumbersome operational requirements
for these smaller entities. Moreover, our
intent is to encourage participation by
not-for-profit, community-based
organizations.
When considering options for the
legal structure of ACOs, we sought to
balance the need for an organization to
be recognized by the State with the need
for flexibility to permit the participants
to select the appropriate organizational
structure for their ACO. We also
considered the importance of
minimizing costs related to organizing
as a specific legal entity. In order to
implement the statutory requirements
that ACOs have a shared governance
mechanism and a formal legal structure
for receiving and distributing shared
payments, we believe that it is necessary
for each ACO to be constituted as a legal
entity appropriately recognized and
authorized to conduct its business
under applicable State law in order to
best achieve the objectives of the Shared
Savings Program and that it must have
a TIN. Therefore, we are proposing to
require an ACO to be an organization
that is recognized and authorized to
conduct its business under applicable
State law and is capable of—(1)
Receiving and distributing shared
savings; (2) repaying shared losses; (3)
establishing, reporting, and ensuring
ACO participant and ACO provider/
supplier compliance with program
requirements, including the quality
performance standards; and (4)
performing the other ACO functions
identified in the statute.
We note that by proposing that the
ACO be required to have a TIN, we are
not proposing to require that the ACO
itself be enrolled in the Medicare
program, in contrast to this requirement
for each ACO participant.
Also, by proposing that each ACO
must be constituted as a legal entity
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appropriately recognized and
authorized under applicable State law,
we are not proposing to require that
existing legal entities appropriately
recognized under State law must form a
separate new entity for the purpose of
participating in the Shared Savings
Program. If the existing legal entity
meets the eligibility requirements to be
an ACO, as described in this proposed
rule, it may operate as an ACO, as long
as it is recognized under applicable
State law and is capable of receiving
and distributing shared savings,
repaying shared losses, and performing
the other ACO functions identified in
the statute and regulations, including
the requirement for shared governance
for ACO participants.
For example, a hospital employing
ACO professionals, which is one of the
entities identified in section 1899(b)(1)
of the Act, may be eligible to participate
in the Shared Savings Program as an
ACO with its current legal structure, as
recognized under applicable State law,
and would not be required to develop a
separate new entity. We recognize,
however, that the absence of a separate
legal entity to operate the ACO may
make it more difficult for us to audit
and otherwise assess ACO performance.
We solicit comment on whether we
should require all ACOs participating in
the Shared Savings Program to be
formed as a distinct legal entity
appropriately recognized and
authorized to conduct its business
under applicable State law or whether
an existing legal entity could be
permitted to participate in the Shared
Savings Program as an ACO, including
entities that have similar arrangements
with other payors. However, we propose
that if an existing entity, such as a
hospital employing ACO professionals
would like to include as ACO
participants other providers of services
and suppliers who are not already part
of its existing legal structure, a separate
entity would have to be established in
order to provide all ACO participants a
mechanism for shared governance and
decision making.
We propose that each ACO would
certify that it is recognized as a legal
entity under State law and authorized
by the State to conduct its business. In
addition, an ACO with operations in
multiple States would have to certify
that it is recognized as a legal entity in
the State in which it was established
and that it is authorized to conduct
business in each State in which it
operates. An ACO must provide in its
application evidence that it is
recognized as a legal entity in the State
in which it was established and that it
is authorized to conduct business in
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each State in which it operates. We
solicit comment on our proposal for the
required legal structure and seek input
on other suitable legal structure
requirements that we should consider
adding in the final rule or through
subsequent rulemaking. Moreover, our
intent is to encourage not-for-profit,
community-based organizations to
participate in the Shared Savings
Program. We request comment on
whether requirements for the creation of
a separate entity would create
disincentives for the formation of ACOs
and whether there is an alternative
requirement that could be used to
achieve the aims of shared governance
and decision making and the ability to
receive and distribute payments for
shared savings.
b. Governance
Although section 1899(b)(1) of the Act
requires that an ACO have a
‘‘mechanism for shared governance’’ and
section 1899(b)(2)(F) of the Act further
requires that an ‘‘ACO shall have in
place a leadership and management
structure that includes clinical and
administrative systems,’’ the statute does
not specify the elements that this shared
governance mechanism or the
accompanying leadership and
management structures must possess.
We believe that such a governance
mechanism should allow for
appropriate proportionate control for
ACO participants, giving each ACO
participant a voice in the ACO’s
decision making process, and be
sufficient to meet the statutory
requirements regarding clinical and
administrative systems. We envision a
mechanism that is transparent,
accountable to the affected beneficiary
community, and also accountable and
responsive to the ACO participants and
the ACO providers/suppliers they
represent. Further, we would anticipate
that the leadership and management
structures would provide for adequate
authority to enable the ACO to execute
its core functions of enhancing the
quality, efficiency, and patientcenteredness of the health care services
furnished to assigned beneficiaries.
Commonly used mechanisms for
establishing shared governance are a
board of directors, board of managers, or
other similar governing bodies that
provide a mechanism for representation
and control in shared decision-making
for all ACO participants. Accordingly,
we are proposing that an ACO must
establish and maintain a governing body
with adequate authority to execute the
statutory functions of an ACO, as
defined by the shared governance
criterion described in more detail later
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in this proposed rule. The governing
body may be a board of directors, board
of managers, or any other governing
body that provides a mechanism for
shared governance and decision-making
for all ACO participants, and that has
the authority to execute the statutory
functions of an ACO, including for
example, to ‘‘define processes to
promote evidence-based medicine and
patient engagement, report on quality
and cost measures, and coordinate care,’’
as required under section 1899(b)(1)(G)
of the Act. As discussed in more detail
later in the document, this governing
body would be comprised of the ACO
participants or their designated
representatives, include Medicare
beneficiaries served by the ACO, and
possess broad responsibility for the
ACO’s administrative, fiduciary, and
clinical operations. While the
representatives on the governing body
could be serving in a similar or
complementary manner for an ACO
participant within the ACO, this body
must be separate and unique to the ACO
when the ACO participants are not
already represented by an existing legal
entity appropriately recognized and
authorized to conduct its business
under applicable State law. In those
instances where the ACO is comprised
of a self-contained financially and
clinically integrated entity that has a
pre-existing board of directors or other
governing body, such as a hospital that
employs ACO professionals, we are also
proposing that the ACO would not need
to form a separate governing body, as
long as that governing body is able to
meet all other criteria required for ACO
governing bodies. In this case, the
integrated entity’s governing body
would be the governing body of the
ACO, and the ACO would be required
to provide in its application evidence
that its pre-existing board of directors or
other governing body, meets all other
criteria required for ACO governing
bodies. Although we wish to provide
potential ACOs with some flexibility on
corporate governance and ACO
formation, we are concerned that
allowing existing entities to be ACOs
would complicate our monitoring and
auditing of the ACO. We solicit
comment on this issue.
Moreover, our intent is to encourage
not-for-profit, community-based
organizations to participate in the
Shared Savings Program. We request
comment on whether requirements for
the creation of a governing body as a
mechanism for shared governance
would create disincentives for the
formation of ACOs and whether there is
an alternative requirement that could be
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used to achieve the aims of shared
governance and decision making.
c. Composition of the Governing Body
For purposes of the Shared Savings
Program, the ACO is, by definition,
comprised of groups of Medicareenrolled providers and suppliers (ACO
participants) that agree to work together
to manage and coordinate care for
beneficiaries, and have established a
mechanism for shared governance—as
opposed to an outside entity directing
their day-to-day operations. Therefore,
we believe that the ACO should be
operated and directed by Medicareenrolled entities that directly provide
health care services to beneficiaries.
Stakeholders have indicated to us that
in the private sector, entrepreneurial
management companies and health
plans have expressed interest in forming
or participating in ACOs. Often, small
groups of providers lack both the capital
and infrastructure necessary to form an
ACO and to administer the
programmatic requirements of the
Shared Savings Program and could
benefit from partnerships with nonMedicare-enrolled entities. For this
reason, we propose that in order to be
eligible for participation in the Shared
Savings Program, the ACO participants
must have at least 75 percent control of
the ACO’s governing body. In addition,
each of the ACO participants must
choose an appropriate representative
from within its organization to represent
them on the governing body. This
proposal ensures that ACOs remain
provider-driven, but also leaves room
for both non-providers and small
provider groups to participate in the
program.
We are requesting comment on this
proposal for whether more or less than
75 percent control of the governing body
being held by the ACO participants is an
appropriate percentage. We are also
requesting comment on whether the
appropriate representative should be
held by persons employed by and
representing Medicare-enrolled TINs.
As discussed in more detail later in
the document, we believe a process for
integrating community resources is an
essential part of patient centeredness.
We are proposing that ACOs be
required to describe how they will
partner with community stakeholders as
part of their application. ACOs that have
a community stakeholder organization
serving on their governing body would
be deemed to have satisfied that
application criterion.
Additionally, as discussed in more
detail later in the document, we are
proposing a requirement that ACOs
provide for beneficiary involvement in
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their governing processes. Specifically,
we are proposing that ACOs will be
required to demonstrate a partnership
with Medicare FFS beneficiaries by
having beneficiary representation in the
ACO governing body.
3. Leadership and Management
Structure
Section 1899(b)(2)(F) of the Act
requires an eligible ACO to ‘‘have in
place a leadership and management
structure that includes clinical and
administrative systems.’’ We believe this
structure should align with and support
the goals of the Shared Savings Program
and the three-part aim of better care for
individuals, better health for
populations, and lower growth in
expenditures. Based on their experience
with the PGP demonstration,
participants identified several factors as
critical to improving quality and the
opportunity to share savings:
• An integrated organization with an
environment that supports expending
resources on multiple programs and
initiatives to improve quality and
reduce unnecessary services.
• Dedicated physician leadership
with a proven ability to motivate
physicians to participate in the
development and implementation of
quality improvement and other clinical
programs and initiatives.
• Health information technology that
facilitates the aggregation and analysis
of data, allows patient-level feedback,
and provides alerts and reminders at the
point of care.
• Experience with non-Medicare
payer initiatives, particularly through a
managed care affiliate, to improve
quality and reduce expenditure growth.
In addition, another important factor
that must be considered is whether the
leadership and management structure of
the ACO should include appropriate
safeguards to ensure the ACO’s
integration and likelihood of achieving
quality improvements and cost
efficiencies. The Antitrust Agencies
have developed criteria to assess
whether collaborations of otherwise
competing health care providers should
be condemned as per se illegal under
antitrust law or subject to a more
thorough evaluation under the ‘‘Rule of
Reason,’’ which would examine likely
procompetitive or anticompetitive
effects.1 To avoid per se condemnation
as ‘‘shams’’ that facilitate price fixing or
other per se illegal activities,
collaborations of competing health care
providers must show that they are
integrated ventures that are likely to, or
1 Arizona v. Maricopa County Medical Society,
457 U.S. 332 (1982).
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do, enable their participants jointly to
achieve cost efficiencies and quality
improvements in providing services.
The efficiency-enhancing integration
‘‘must likely generate procompetitive
benefits that enhance the participants’
ability or incentives to compete, and
thus offset any anticompetitive
tendencies of the arrangement.’’ 2
Accordingly, the antitrust perspective
focuses on how collaboration, including
coordinated care, can lower costs and
improve quality, just as the intent of the
Shared Savings Program under section
1899 of the Act is to promote
accountability for Medicare
beneficiaries, improve the coordination
of FFS items and services, and
encourage investment in infrastructure
and redesigned care processes for high
quality and efficient service delivery.
For antitrust purposes, collaborations of
competing health care providers may
use either financial or clinical
integration, or both, as means to achieve
cost efficiencies and quality
improvements.3 To demonstrate
financial integration, participants in
collaboration must share substantial
financial risk, so they have the incentive
to cooperate in controlling costs and
improving quality by managing the
provision of services.4 To demonstrate
clinical integration, participants must
show a degree of interaction and
interdependence among providers in
their provision of medical services that
enables them to jointly achieve cost
efficiencies and quality improvements.5
The Federal Antitrust Agencies have
concluded that successfully achieving
clinical integration requires the
establishment and operation of active
and ongoing processes and mechanisms
to facilitate, encourage, and assure the
necessary cooperative interaction.6
We believe that these criteria also
provide insight into the leadership and
management structures, including
clinical and administrative systems,
necessary for ACOs to achieve the threepart aim of better care for individuals,
better health for populations, and lower
growth in expenditures. We also note
that these criteria are very similar to the
2 Letter from Jeffrey Brennan, Assistant Director,
Bureau of Competition, Federal Trade Commission
to John J. Miles, Ober, Kaler, Grimes & Shriver
(February 19, 2002), available at https://www.ftc.gov/
bc/adops/medsouth.shtm.
3 Department of Justice and Federal Trade
Commission, Statements of Antitrust Enforcement
Policy in Health Care, Statement 8 (1996), available
at https://www.ftc.gov/reports/hlth3s.pdf.
4 Id.
5 See, for example, Letter from Markus Meier to
John J. Miles, Ober, Kaler, Grimes & Shriver 7 (June
18, 2007), available at https://www.ftc.gov/bc/adops/
070618mewdsouth.pdf.
6 Id.
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factors identified previously by
participants in the PGP demonstration
as critical to improving quality and
controlling the cost of health care.
Similarly, antitrust analyses have
examined whether participants in such
a collaboration are committed to the
collective development and
implementation of evidence-based
protocols and benchmarks, to individual
and group accountability for adherence
to those protocols and benchmarks, to
the development of technology to
facilitate providers’ compliance, to the
measurement of compliance with those
protocols, and to improved performance
with respect to benchmarks, among
other things.7
It is in the public interest to
harmonize the eligibility criteria for
ACOs that wish to participate in the
Shared Savings Program with the
similar antitrust criteria on clinical
integration. As discussed in more detail
in section II. I. of this proposed rule,
competition between ACOs is expected
to have significant benefits for Medicare
beneficiaries, by improving the quality
of care they receive, protecting their
access to a variety of providers, and
helping to sustain the Medicare program
by controlling costs. Furthermore,
because ACOs that operate in the
Shared Savings Program are likely to
use the same organizational structure
and clinical care practices to serve both
Medicare beneficiaries and consumers
covered by commercial insurance, the
certainty created by harmonizing our
eligibility criteria with antitrust
requirements will help to ensure that an
ACO organization participating in the
Shared Savings Program will not
subsequently face an antitrust challenge
that its conduct is per se illegal, which
could prevent the ACO from fulfilling
the 3-year term of its agreement under
the Shared Savings Program.
Accordingly, we believe an ACO, the
ACO participants, and ACO providers/
suppliers should demonstrate an
organizational commitment to the
Shared Savings Program and the terms
of the 3-year agreement, both as a group
and individually, as well as the
leadership and management capabilities
7 See, for example, Letter from Markus H. Meier,
Assistant Director, Bureau of Competition, Federal
Trade Commission to Christi J. Braun, Ober, Kaler,
Grimes & Shriver 8 (April 13, 2009), available at
https://www.ftc.gov/os/closings/staff/
090413tristateaoletter.pdf; Letter from Markus H.
Meier, Assistant Director, Bureau of Competition,
Federal Trade Commission to Christi J. Braun &
John J. Miles, Ober, Kaler, Grimes & Shriver 7 (Sept.
17, 2007), available at https://www.ftc.gov/bc/adops/
gripa.pdf; Letter from Jeffrey Brennan, Assistant
Director, Bureau of Competition, Federal Trade
Commission to John J. Miles, Ober, Kaler, Grimes
& Shriver (Feb. 19, 2002), available at https://
www.ftc.gov/bc/adops/medsouth.shtm.
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necessary to achieve the three-part aim
by managing and coordinating the care
of assigned Medicare beneficiaries. We
note that the statute permits ACO
participants that form an ACO to use a
variety of collaborative organizational
structures, including collaborations
short of merger, to evidence the required
organizational commitment and
leadership and management
capabilities.
Thus, consistent with the requirement
in section 1899(b)(2)(F) of the Act that
an ACO have a leadership and
management structure that includes
clinical and administrative systems, we
are proposing that ACOs meet the
following criteria:
• The ACO’s operations would be
managed by an executive, officer,
manager, or general partner, whose
appointment and removal are under
control of the organization’s governing
body and whose leadership team has
demonstrated the ability to influence or
direct clinical practice to improve
efficiency processes and outcomes.
• Clinical management and oversight
would be managed by a senior-level
medical director who is a boardcertified physician, licensed in the State
in which the ACO operates, and
physically present in that State.
• ACO participants and ACO
providers/suppliers would have a
meaningful commitment to the ACO’s
clinical integration program to ensure
its likely success. Meaningful
commitment may include, for example,
a meaningful financial investment in the
ACO, or a meaningful human
investment (for example, time and
effort) in the ongoing operations of the
ACO such that the potential loss or
recoupment of the investment is likely
to motivate the participant to make the
clinical integration program succeed.
• The ACO would have a physiciandirected quality assurance and process
improvement committee that would
oversee an ongoing quality assurance
and improvement program. The quality
assurance program would establish
internal performance standards for
quality of care and services, cost
effectiveness, and process and outcome
improvements, and hold ACO
providers/suppliers accountable for
meeting the performance standards. The
program would also have processes and
procedures in place to identify and
correct poor compliance with such
standards and to promote continuous
quality improvement.
• The ACO would develop and
implement evidence-based medical
practice or clinical guidelines and
processes for delivering care consistent
with the goals of better care for
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individuals, better health for
populations, lower growth in
expenditures. The guidelines and care
delivery processes would cover
diagnoses with significant potential for
the ACO to achieve quality and cost
improvements, taking into account the
circumstances of the individual
beneficiary, and could be accomplished,
for example, through an integrated
electronic health record with clinical
decision support. ACO participants and
ACO providers/suppliers would have to
agree to comply with these guidelines
and processes and to be subject to
performance evaluations and potential
remedial actions.
• The ACO would have an
infrastructure, such as information
technology, that enables the ACO to
collect and evaluate data and provide
feedback to the ACO providers/
suppliers across the entire organization,
including providing information to
influence care at the point of care via,
for example, shared clinical decision
support, feedback from patient
experience of care surveys or other
internal or external quality and
utilization assessments.
As discussed later in the document,
and in section II. C. of this proposed
rule, it is our expectation that ACO
participants and ACO providers/
suppliers participating in the ACO
would make a commitment to
participate in the ACO for not less than
3 years. However, we recognize it will
be necessary for the ACO to include a
remedial process for ACO participants
that fail to comply with the ACO’s
internal procedures and performance
standards, including the possibility of
expulsion of significant outliers. We
caution that expulsion cannot be used
as a mechanism to avoid at-risk
beneficiaries.
In order to determine an ACO’s
compliance with these requirements, as
part of the application process, we are
proposing that an ACO would submit all
of the following:
• ACO documents (for example,
participation agreements, employment
contracts, and operating policies) that
describe the ACO participants’ and ACO
providers/suppliers’ rights and
obligations in the ACO, the shared
savings that will encourage ACO
participants and ACO providers/
suppliers to adhere to the quality
assurance and improvement program
and the evidenced-based clinical
guidelines;
• Documents that describe the scope
and scale of the quality assurance and
clinical integration program, including
documents that describe all relevant
clinical integration program systems
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and processes, such as the internal
performance standards and the
processes for monitoring and evaluating
performance;
• Supporting materials documenting
the ACO’s organization and
management structure, including an
organizational chart, a list of committees
(including names of committee
members) and their structures, and job
descriptions for senior administrative
and clinical leaders; and
• Evidence that the ACO has a boardcertified physician as its medical
director who is licensed in the State in
which the ACO resides and that a
principal CMS liaison is identified in its
leadership structure.
• Evidence that the governing body
includes persons who represent the
ACO participants, and that these ACO
participants hold at least 75 percent
control of the governing body.
Additionally, upon request, the ACO
would also be required to provide
copies of the following documents:
• Documents effectuating the ACO’s
formation and operation, including
charters, by-laws, articles of
incorporation, and partnership, joint
venture, management, or asset purchase
agreements.
• Descriptions of the remedial
processes that will apply when ACO
participants and ACO providers/
suppliers fail to comply with the ACO’s
internal procedures and performance
standards, including corrective action
plans and the circumstances under
which expulsion could occur.
In an effort to allow flexibility and
innovation, we are proposing that ACOs
with innovative leadership and
management structures have the
opportunity to describe an alternative
mechanism for how their leadership and
management structure would conduct
the activities noted previously in order
to achieve the same goals so that they
may be given consideration in the
application process. That is, an
organization that does not have one or
more of the following: An executive,
officer, manager, or general partner;
senior-level medical director; or
physician-directed quality assurance
and process improvement committee,
would be required in its application to
describe how the ACO will perform
these functions without such
leadership. For example, if an ACO does
not have a physician-directed quality
assurance and process improvement
committee, the ACO would need to
describe how it plans to oversee an
ongoing quality assurance and
improvement program as described
previously. Additionally, we seek
comment on the requirement for
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submission of certain documents as
noted previously and whether an
alternative method could be used to
verify compliance with requirements.
We request comment on the proposed
leadership and management structure
and whether the compliance burden
associated with these requirements will
discourage participation, hinder
innovative organizational structures, or
whether there are other or alternative
leadership and management
requirements that would enable these
organizations in meeting the three-part
aim.
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4. Accountability for Beneficiaries
Section 1899(b)(2)(A) of the Act
requires participating ACOs to ‘‘be
willing to become accountable for the
quality, cost, and overall care of the
Medicare fee-for-service beneficiaries
assigned to it.’’ To satisfy this
requirement, we are proposing that an
ACO executive who has the authority to
bind the ACO must certify to the best of
his or her knowledge, information, and
belief that the ACO participants are
willing to become accountable for, and
to report to us on, the quality, cost, and
overall care of the Medicare FFS
beneficiaries assigned to the ACO. The
certification would be included as part
of the ACO’s application and 3-year
participation agreement.
5. Agreement Requirement
Section 1899(b)(2)(B) of the Act
requires participating ACOs to ‘‘enter
into an agreement with the Secretary to
participate in the program for not less
than a 3-year period * * *.’’ For the first
round of the Shared Savings Program,
we are proposing to limit participation
agreements to a 3-year period. We are
seeking comments on this proposal and
whether a longer agreement period
should be considered initially.
If the ACO is approved for
participation, we propose that an
authorized representative—specifically,
an executive who has the ability to bind
the ACO, must certify to the best of his
or her knowledge, information, and
belief that the ACO participants agree to
the requirements set forth in the 3-year
agreement between the ACO and us—
sign a 3-year participation agreement
and submit the signed agreement to us.
This participation agreement would
include an acknowledgment that the
ACO agrees to comply with all of the
requirements for participation in the
Shared Savings Program and that all
contracts or arrangements between or
among the ACO, ACO participants, ACO
providers/suppliers, and other entities
furnishing services related to ACO
activities must require compliance with
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the ACO’s obligations under the 3-year
agreement. The participation agreement
would be signed by an authorized
representative of the ACO after it has
been approved for participation. The
ACO would be responsible for providing
a copy of the agreement to its ACO
participants and ACO providers/
suppliers. We are soliciting comment on
this proposal, including any additional
measures or alternative means that we
should consider to fulfill this
requirement.
We also recognize that, while having
signed a 3-year participation agreement
with us in good faith and with the
intention to participate in the program
for the full 3-year agreement period,
there may be instances where an ACO
might need to discontinue its
participation in the Shared Savings
Program prior to the end of the
agreement period. As described in
section II. H. Monitoring and
Termination of ACOs of this proposed
rule, we propose to require an ACO to
give us 60 days advance written notice
of its intention to terminate its
agreement to participate in the Shared
Savings Program and the effective date
of its termination. As described in more
detail in section II. F of this proposed
rule, we propose the ACO will be
subject to a 25 percent withhold of
shared savings in order to offset any
future losses under the two-sided
model. We propose that if an ACO
completes its 3-year agreement
successfully, we will refund in full any
portion of shared savings withheld
during the course of the 3-year
agreement period that is not needed to
offset losses. We further propose that in
the event an ACO’s 3-year agreement is
terminated before the completion of the
3 years, we will retain any portion of
shared savings withheld.
Finally, it is our intention that all
ACOs, ACO participants, and ACO
providers/suppliers with direct or
indirect obligations under the Shared
Savings Program be subject to the
requirements of the agreement between
the ACO and CMS and that all
certifications submitted on behalf of the
ACO in connection with the Shared
Savings Program application,
agreement, shared savings distribution,
as discussed in section II. F. or
otherwise extend to all parties with
obligations to which the particular
certification applies.
We are considering the best way to
achieve this end and solicit public
comments on this issue.
6. Distribution of Savings
As discussed previously, an ACO
must be a legal entity appropriately
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recognized and authorized to conduct
its business under State law, and would
be identified by a TIN. We propose to
make any shared savings payments
directly to the ACO as identified by its
TIN. The TIN associated with the ACO’s
legal entity may, or may not, be enrolled
in the Medicare program, unlike the
ACO participant TINs that are Medicareenrolled groups of providers of services
and suppliers. Therefore, because the
statute contemplates payment directly
to the ACO, we are proposing to pay the
ACO TIN directly. We acknowledge that
this proposal could raise program
integrity concerns, because allowing
shared savings payments to be made
directly to a non-Medicare-enrolled
entity would likely impede the
program’s ability to recoup
overpayments as there would be no
regular payments that could be offset.
This is part of the rationale for the
payment withhold described in more
detail in section II. F, Shared Savings
Determination, as well as the other
safeguards for assuring ACO repayment
of shared losses described in section
II.G.of this proposed rule. We solicit
comments on our proposal to make
shared savings payments directly to the
ACO, as identified by its TIN. In
addition, we are soliciting comment on
our proposal to make shared savings
payments to a non-Medicare-enrolled
entity.
While section 1899(b)(2)(C) of the Act
requires an ACO to have a formal legal
structure that would allow the
organization to receive and distribute
payments for shared savings to
participating providers of services and
suppliers, the statute does not establish
any requirements for the manner in
which shared savings payments are
distributed. We have considered
whether it would be appropriate, under
the broad discretion granted to the
Secretary in implementing the Shared
Savings Program, to propose criteria for
the distribution of shared savings by the
ACO. Although we do not believe we
have the authority to specify how
shared savings must be distributed (so
long as the distribution is consistent
with all applicable legal requirements),
we believe it would be consistent with
the purpose and intent of the statute to
require the ACO to indicate as part of
its application how it plans to use
potential shared savings to meet the
goals of the program. More specifically,
ACOs would have to indicate how
potential shared savings would be used
to promote accountability for their
Medicare population and the
coordination of their care as well as how
they might be invested in infrastructure
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and redesigned care processes for high
quality and efficient health care service
delivery. Therefore, we propose to
require ACOs to provide a description
in their application of the criteria they
plan to employ for distributing shared
savings among ACO participants and
ACO providers/suppliers, and how any
shared savings will be used to align
with the aims of better care for
individuals, better health for
populations, and lower growth in
expenditures. We believe the proposed
requirement would achieve the most
appropriate balance among objectives
for encouraging participation,
innovation, and achievement of program
while still focusing on the aims of better
care for individuals, better health for
populations, and lower growth in
expenditures. Additionally, it is the
intention of this requirement for ACOs
to include this description in the
application, to both guard against
improper financial incentives as well as
ensure appropriate beneficiary
protections.
7. Sufficient Number of Primary Care
Providers and Beneficiaries
Section 1899(b)(2)(D) of the Act
requires participating ACOs to ‘‘include
primary care ACO professionals that are
sufficient for the number of Medicare
fee-for-service beneficiaries assigned to
the ACO * * *’’ and that at a minimum,
‘‘the ACO shall have at least 5,000 such
beneficiaries assigned to it * * *’’
Physician patient panels can vary
widely in the number of FFS Medicare
beneficiaries served. In section II. C. of
this proposed rule, we discuss our
proposal to assign beneficiaries to an
ACO on the basis of primary care
services rendered by physicians with
primary care specializations in general
practice, internal medicine, family
practice, and geriatric medicine. We are
proposing that this algorithm will also
be used to assign beneficiaries during
the baseline years in order to establish
a historical per capita cost benchmark
against which the ACO would be
evaluated during each year of the
agreement period. We believe it is
reasonable to assume that if by using
this algorithm the ACO demonstrates a
sufficient number of beneficiaries to
fulfill this eligibility requirement for
purposes of establishing a benchmark,
then the ACO also contains a sufficient
number of primary care professionals to
provide care to these beneficiaries. It is
also reasonable to assume the ACO
would continue to approximate this
number in each year of the agreement
period. Thus, we are proposing that for
purposes of eligibility under section
1899(b)(2)(D) of the Act, an ACO would
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be determined to have a sufficient
number of primary care ACO
professionals to serve the number of
Medicare beneficiaries assigned to it if
the number of beneficiaries historically
assigned over the three-year
benchmarking period using the ACO
participant TINs exceeds the 5,000
threshold for each year. We are
soliciting comment on this proposal as
well as any additional guidance that
could be considered for meeting these
requirements.
While an ACO could meet the
requirements in section 1899(b)(2)(D) of
the Act when it applies to participate in
the Shared Savings Program, the
number of assigned beneficiaries could
fall below the 5,000 level due to either
significant events, such as when an
ACO professional or group of
professionals cease to participate in the
ACO, or in those instances where the
actual number of beneficiaries is close
to 5,000 as a result of normal
fluctuations in patient populations. The
requirements under section
1899(b)(2)(D) of the Act are important
with respect both to the sufficiency of
the ACO to provide primary care
services to its assigned beneficiary
population and statistical stability for
purposes of calculating per capita
expenditures and assessing quality
performance. Simply stated, and as
described in detail in section II.D. of
this proposed rule, as the number of
assigned beneficiaries increases, the
minimum savings rate (MSR) gets
smaller. Conversely, as the number of
assigned beneficiaries decreases, the
MSR expands thus making it
significantly more difficult for an ACO
to obtain shared savings. So, retaining
5,000 assigned beneficiaries is
important from both the perspective of
the capacity of the ACO to provide
primary care services to its assigned
beneficiary population as well as the
ability of the ACO to realize shared
savings by exceeding the MSR.
Thus, we considered what action, if
any, should be taken in the event the
number of beneficiaries falls below
5,000. Specifically, we considered
whether an ACO’s participation in the
program should be terminated or its
eligibility for shared savings be deferred
if the number of beneficiaries dropped
below 5,000. We considered terminating
the ACO for falling below 5,000
beneficiaries immediately or after giving
the ACO an opportunity to implement a
corrective action plan. We have
concerns that immediately terminating
an ACO or denying it an opportunity to
share in savings because its population
fell slightly may discourage
participation among smaller ACOs. We
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believe this would be inconsistent with
the goals of allowing greater
opportunities for broadly transforming
the health care delivery system and
increasing access to high quality and
lower cost care under the Shared
Savings Program for Medicare
beneficiaries regardless of where they
live. Another option would be to take no
action if the ACO falls below 5,000
assigned beneficiaries. Taking no action
in these instances would be inconsistent
with the statutory requirement that an
ACO have 5,000 assigned beneficiaries
in order to be eligible to participate in
the Shared Savings Program and would
reduce incentives for smaller provider
organizations to affiliate with other
providers and suppliers to be successful
under the Shared Savings Program. A
third option might be to adjust, or scale,
the shared savings in those instances
where the number of assigned
beneficiaries falls below the floor of
5,000 over the course of a performance
year. If shared savings are realized, and
all other requirements of participation
are met, an ACO that falls below the
5,000 assigned beneficiary floor could
realize shared savings but at a reduced
rate of savings that would parallel the
number of beneficiaries assigned to the
ACO. Thus, the amount of the incentive
payment would be scaled to the number
of beneficiaries in the ACO during the
performance year. However, since the
MSR adjusts with the number of
assigned beneficiaries, there is a built-in
incentive for ACOs to increase their
beneficiary population.
We believe a reasonable compromise
would balance the statutory
requirements, program incentives, and
recognition of expected variation in an
ACO’s assigned population. Thus, we
are proposing that if an ACO’s assigned
population falls below 5,000 during the
course of the agreement period, we
would issue a warning and place the
ACO on a corrective action plan. The
ACO would remain eligible for shared
savings for the performance year for
which the warning was issued. We
further propose that if the ACO fails to
meet the eligibility criterion of having
more than 5,000 beneficiaries by the
completion of the next performance
year, the ACO’s participation agreement
will be terminated and the ACO will not
be eligible to share in savings for that
year. Thus, for example, if during the
first performance year, an ACO’s
assigned population fell below 5,000,
we would issue a warning, notifying the
ACO of the variation in their assigned
population. The ACO would be placed
on a corrective action plan which could
include, for example, a plan to add more
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primary care providers to the ACO. The
ACO would remain eligible to share in
savings for the first performance year.
However, if the ACO’s assigned
population had not returned to at least
5,000 by the end of the second
performance year, then that ACO’s
agreement will be terminated and the
ACO would not be eligible to share in
savings for the second performance
year. We also propose to reserve the
right to review the status of the ACO
while on the corrective action plan and
terminate the agreement on the basis
that the ACO no longer meets eligibility
requirements. We request comment on
this proposal and on other potential
options for addressing situations where
the assigned beneficiary population falls
below 5,000 during the course of an
agreement period.
8. Required Reporting on Participating
ACO Professionals
Section 1899(b)(2)(E) of the Act
requires ACOs to ‘‘provide the Secretary
with such information regarding ACO
professionals participating in the ACO
as the Secretary determines necessary to
support the assignment of Medicare FFS
beneficiaries to an ACO, the
implementation of quality and other
reporting requirements * * *, and the
determination of payments for shared
savings * * *.’’ As discussed in sections
II.B. and II.D. of this proposed rule, we
are proposing to define an ACO
operationally as a legal entity that is
comprised of a group of ACO
participants which are in turn defined
to mean Medicare-enrolled providers or
suppliers, as identified by their TINs.
However, TIN level data alone may not
be entirely sufficient for a number of
purposes in the Shared Savings Program
such as implementing our methodology
for beneficiary assignment and
calculating the quality performance
score. Accordingly, to satisfy the
requirements under section
1899(b)(2)(E) of the Act, we are
proposing that entities applying to
participate in the Shared Savings
Program must provide not only the TINs
of the ACO and the ACO participants,
but also a list of national provider
identifiers (NPIs) associated with the
ACO providers/suppliers, which
separately identifies the physicians that
provide primary care.
We are also proposing to require an
ACO to maintain, update, and annually
report to us the TINs of its ACO
participants and the NPIs associated
with the ACO providers/suppliers. We
believe that requiring this information
offers the level of transparency needed
to implement the Shared Savings
Program.
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9. Processes To Promote Evidence-Based
Medicine, Patient Engagement,
Reporting, and Coordination of Care
Section 1899(b)(2) of the Act
establishes a number of requirements
which ACOs must satisfy in order to be
eligible to participate in the Shared
Savings Program. Several of these
standards deal with how patient care is
provided by the ACO, with a focus on
processes and methods to: (1) Promote
higher quality of care; (2) better
coordinate care; and (3) meet the needs
and concerns of patients and their
families, including effectively engaging
patients and their families in medical
decision-making. Specifically, section
1899(b)(2)(G) of the Act requires an
ACO to ‘‘define processes to promote
evidence-based medicine and patient
engagement, report on quality and cost
measures, and coordinate care, such as
through the use of telehealth, remote
patient monitoring, and other such
enabling technologies.’’
With regard to each of the specific
requirements under section
1899(b)(2)(G) of the Act, we have two
options. One option is simply to
propose to require documentation of an
ACO’s plans to ‘‘define processes to
promote evidence-based medicine and
patient engagement, report on quality
and cost measures, and coordinate care,
such as through the use of telehealth,
remote patient monitoring, and other
such enabling technologies.’’ Under this
option, we would not establish any
more specific criteria for these
requirements. However, we would
expect that the required documentation
present convincing evidence of concrete
and effective plans to satisfy these
requirements, by providing specific
processes and criteria that the ACO
intends to use for promoting, improving,
and assessing evidence-based medicine,
beneficiary engagement, reporting of
quality and cost measures, and
coordination of care. Such processes
would have to include provisions for
internal assessment of cost and quality
of care within the ACO, and employ
these assessments in continuous
improvement of the ACO’s care
practices.
The other option is to identify specific
criteria that we would propose to
require ACOs to meet with regard to
each of these requirements. For
example, with regard to the requirement
to promote evidence-based medicine,
we could provide a detailed description
of evidence-based guidelines for various
conditions and diseases for which we
would hold ACOs accountable,
including specific instructions for how
an ACO would demonstrate it is
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following these guidelines and
monitoring compliance among its ACO
participants and ACO providers/
suppliers. We could also specify a
number of conditions for which the
ACO would maintain an evidence-based
medicine preventive health guidelines
program. Similarly, we could identify
and require the use of specific decision
support tools, patient activation
measures, or other patient support tools
in order for an ACO to satisfy the
requirement for beneficiary engagement.
However, we have concerns that a
prescriptive approach would be
premature and potentially impede
innovation and the goals of this
program. Thus, for the requirements
under section 1899(b)(2)(G) of the Act,
we are proposing that in order to be
eligible to participate in the Shared
Savings Program, the ACO provide
documentation in its application
describing its plans to: (1) Promote
evidence-based medicine; (2) promote
beneficiary engagement; (3) report
internally on quality and cost metrics;
and (4) coordinate care. We are
proposing this option in order to allow
ACOs the flexibility to choose the tools
for meeting these requirements that are
most appropriate for their practitioners
and patient populations. Over time, as
we learn more about successful
strategies in these areas, and as we have
more experience assessing specific
critical elements for success, the Shared
Savings Program eligibility
requirements with regard to section
1899(b)(2)(G) of the Act may be revised.
We are also specifically soliciting
comment on whether more prescriptive
criteria may be appropriate for meeting
some or all of these requirements under
section 1899(b)(2)(G) of the Act for
future rulemaking. Later in the
document, we discuss the concepts of
evidence-based medicine, patient
engagement, internal quality and cost
reporting, and coordination of care, and
describe how Shared Savings Program
applicants can establish compliance
with the requirements of section
1899(b)(2)(G) of the Act.
a. Processes To Promote Evidence-Based
Medicine
As stated previously, section
1899(b)(2)(G) of the Act requires an
ACO to ‘‘define processes to promote
evidence-based medicine * * *.’’
Evidence-based medicine can be
generally defined as the application of
the best available evidence gained from
the scientific method to clinical
decision-making. It seeks to assess the
strength of evidence of the risks and
benefits of treatments (including lack of
treatment) and diagnostic tests, and
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applies this evidence to the processes of
medical decision-making and treatment.
In practice, such an approach should
involve the establishment and
implementation of evidence-based
guidelines, based on the best available
evidence concerning the effectiveness of
medical treatments, at the
organizational or institutional level. A
genuine evidence-based approach
would also involve regularly assessing
and updating such guidelines to
promote continuous improvement in the
quality of care in light of new evidence
concerning the effectiveness of medical
treatments. We propose that as part of
the application, the ACO would
describe the evidence-based guidelines
it intends to establish, implement, and
periodically update.
b. Processes To Promote Patient
Engagement
Section 1899(b)(2)(G) of the Act also
requires an ACO to ‘‘define processes to
promote * * * patient engagement.’’
The term ‘‘patient engagement’’ is the
active participation of patients and their
families in the process of making
medical decisions. Patient engagement
in decision-making requires
consideration not only of the best
scientific evidence concerning medical
treatment, but also the opportunity for
patients and families to assess
prospective treatment approaches in the
light of their own values and
convictions. Measures for promoting
patient engagement may include, but are
not limited to, the use of decision
support tools and shared decision
making methods with which the patient
can assess the merits of various
treatment options in the context of his
or her values and convictions. Patient
engagement also includes methods for
fostering what might be termed ‘‘health
literacy’’ in patients and their families.
Health literacy is the possession of basic
knowledge about maintaining good
health, avoiding preventable medical
conditions, managing existing
conditions, as well as knowledge about
how the care system works (for
example, the roles of primary care
physicians and specialist physicians,
the nature and operation of both public
and private health insurance, etc.).
We propose that as part of the
application, the ACO would describe
the patient engagement processes it
intends to establish, implement, and
periodically update.
c. Processes To Report on Quality and
Cost Measures
Section 1899(b)(2)(G) of the Act
requires an ACO to ‘‘define processes to
* * * report on quality and cost
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measures.’’ Processes that may be used
for reporting on quality and cost
measures may include, but are not
limited to, developing a population
health data management capability, or
implementing practice and physician
level data capabilities with point-ofservice (POS) reminder systems to drive
improvement in quality and cost
outcomes. We would expect ACOs to be
able to monitor both costs and quality
internally and make appropriate
modifications based upon their
collection of such information.
We propose that as part of the
application, the ACO would describe its
process to report internally on quality
and cost measures, and how it intends
to use that process to respond to the
needs of its Medicare population and to
make modifications in its care delivery.
d. Processes To Promote Coordination of
Care
Finally, section 1899(b)(2)(G) of the
Act requires an ACO to ‘‘define
processes to * * * coordinate care, such
as through the use of telehealth, remote
patient monitoring, and other such
enabling technologies.’’ Coordination of
care involves strategies to promote,
improve, and assess integration and
consistency of care across primary care
physicians, specialists, and acute and
post-acute providers and suppliers,
including methods to manage care
throughout an episode of care and
during its transitions, such as discharge
from a hospital or transfer of care from
a primary care physician to a specialist.
Compliance with this requirement may
involve a range of strategies which may
include the following examples:
• A capability to use predictive
modeling to anticipate likely care needs.
• Utilization of case managers in
primary care offices.
• Having a specific transition of care
program that includes clear guidance
and instructions for patients, their
families, and their caregivers.
• Remote monitoring.
• Telehealth.
• The establishment and use of health
information technology, including
electronic health records and an
electronic health information exchange
to enable the provision of a beneficiary’s
summary of care record during
transitions of care both within and
outside of the ACO.
The provisions of any free services
(telehealth, case managers, etc.) between
parties in a position to generate Federal
health care program referrals could
trigger evaluation under the relevant
fraud and abuse laws. Stakeholders
interested in this issue may also wish to
comment on the joint OIG/CMS notice
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referenced in section II.I of this
proposed rule.
The strategies employed by an ACO to
optimize care coordination should not
impede the ability of a beneficiary to
seek care from providers that are not
participating in the ACO, or develop
policies to place any restrictions that are
not legally required on the exchange of
medical records with providers who are
not part of the ACO. We are proposing
to prohibit the ACO from developing
any policies that would restrict a
beneficiary’s freedom to seek care from
providers and suppliers outside of the
ACO.
10. Patient-Centeredness Criteria
Section 1899(b)(2)(H) of the Act
requires an ACO to ‘‘demonstrate to the
Secretary that it meets patientcenteredness criteria specified by the
Secretary, such as the use of patient and
caregiver assessments or the use of
individualized care plans.’’ A patientcentered, or person-centered,
orientation could be defined as care that
incorporates the values (to the extent
the informed, individual patient desires
it) of transparency, individualization,
recognition, respect, dignity, and choice
in all matters, without exception,
related to one’s person, circumstances,
and relationships in health care. Patientcentered care should extend not only to
the patient but to the family and
caregivers of the patient. Patientcenteredness is one of the Institute of
Medicine’s (IOM’s) aims for
improvement in health care. In IOM’s
report ‘‘Crossing the Quality Chasm: A
New Health System for the 21st
Century,’’ providing patient-centered
care is defined as ‘‘providing care that is
respectful of and responsive to
individual patient preferences, needs,
and values, and ensuring that patient
values guide all clinical decisions.’’ (to
view IOM’s report discussed previously,
visit https://iom.edu/Reports/2001/
Crossing-the-Quality-Chasm-A-NewHealth-System-for-the-21stCentury.aspx) The National Partnership
for Women and Families suggests the
following principles for patient-centered
care: (1) Care is comprehensive,
coordinated, personalized, and planned;
(2) patients’ experience of care is
routinely assessed and improved; (3)
patients and their caregivers are full
partners in their care; (4) transitions
between settings of care are smooth,
safe, effective, and efficient; (5) patients
can get care when and where they need
it; (6) care is integrated with the
community resources patients need to
maintain health and wellbeing; and (7)
continuous quality improvement and
elimination of disparities are top
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priorities. (To view the Statement of
Debra L. Ness, President, Nat’l
Partnership for Women & Families,
Senate Finance Committee, Roundtable
on Delivery System Reform April 21,
2009 visit https://www.national
partnership.org/site/DocServer/090421_
SenateFinanceRoundtableStatement
_Ness.pdf?docID=4881)
The statutory requirement for
‘‘patient-centeredness criteria’’ clearly
implies that one goal of the Shared
Savings Program is for ACOs to adopt a
focus on patient-centeredness that is
promoted by the governing body and
integrated into practice by leadership
and management working with the
organization’s health care teams.
Drawing from the perspectives
discussed previously, we believe the
following list of proposed patientcenteredness principles should inform
the care provided by an ACO
participating in the Shared Savings
Program:
• Care should be individualized
based on the person’s unique needs,
preferences, values, and priorities.
• Beneficiaries should have access to
their own medical records and to
clinical knowledge so that they may
make informed choices about their care.
• Beneficiaries (and their caregivers
and/or family members where
applicable) should be encouraged to be
partners in care and make choices
regarding the care they receive, based on
both the medical record and clinical
knowledge (that is, evidence-based
medicine) provided by their ACO and
the beneficiary’s individual values.
• Beneficiary and caregiver and/or
family experience of care should be
routinely assessed and the ACO should
seek to improve it where opportunities
for improvement are identified.
• Care should be integrated with the
community resources beneficiaries
require to maintain well-being.
• Transitions in care among providers
in the ACO, as well as other providers
outside the ACO from whom the
beneficiaries may also seek care, should
be supported consistent with the
patient-centeredness goals of
coordinating care and having
information follow patients by, for
example, developing processes for the
electronic exchange of information.
In the light of these principles, we
believe the following processes and
actions listed later in the document
would be necessary to ensure the
patient-centered orientation required by
section 1899. We propose that an ACO
would be considered patient-centered if
it has all of the following:
• A beneficiary experience of care
survey in place and a description in the
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ACO application how the ACO will use
the results to improve care over time. As
discussed in more detail later in the
document, and as proposed in section
II.E. of this proposed rule, scoring on
this survey would help the ACO meet
the quality performance standard.
• Patient involvement in ACO
governance. As discussed in more detail
later in the document, the ACO would
be required to have a Medicare
beneficiary on the governing board.
• A process for evaluating the health
needs of the ACO’s assigned population,
including consideration of diversity in
their patient populations, and a plan to
address the needs of their population.
As discussed in more detail later in this
document, the ACO would be required
to describe this process as part of the
application and describe how it would
consider diversity in its patient
population and plans to address its
population needs.
• Systems in place to identify highrisk individuals and processes to
develop individualized care plans for
targeted patient populations, including
integration of community resources to
address individual needs. This proposal
and application requirements are
discussed in more detail later in this
document.
• A mechanism in place for the
coordination of care (for example, via
use of enabling technologies or care
coordinators). The ACO would be
required to describe its mechanism for
coordinating care for Medicare
beneficiaries. In addition, the ACO
should have a process in place (or clear
path to develop such a process) to
electronically exchange summary of
care information when patients
transition to another provider or setting
of care, both within and outside the
ACO, consistent with meaningful use
requirements under the EHR Incentive
program. The ACO would be required to
describe their process or their plan to
develop a process to electronically
exchange summary of care information
during care transitions. Additionally, in
section II.E. of this proposed rule, we
propose to include care transitions
measures as part of the assessment of
ACO quality.
• A process in place for
communicating clinical knowledge/
evidence-based medicine to
beneficiaries in a way that is
understandable to them. This process
should allow for beneficiary engagement
and shared decision-making that takes
into account the beneficiaries’ unique
needs, preferences, values, and
priorities. The ACO would be required
to describe its process, as discussed in
section II.E. of this proposed rule, for
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communicating clinical knowledge/
evidence-based medicine and describe
how the ACO providers/suppliers will
engage the beneficiary in shared
decision-making.
• Written standards in place for
beneficiary access and communication
and a process in place for beneficiaries
to access their medical record. As part
of its application, the ACO would be
required to submit its written standards
for beneficiary access and
communication. Additionally, the ACO
would be required to describe its
process for beneficiaries to access their
medical record.
• Internal processes in place for
measuring clinical or service
performance by physicians across the
practices, and using these results to
improve care and service over time. As
described previously, the documents
submitted to meet leadership and
management criteria related to quality
assurance and clinical integration
program would satisfy this patientcenteredness criterion.
We believe that this list provides a
comprehensive set of criteria for
realizing and demonstrating patientcenteredness in the operation of an
ACO. Accordingly, we are proposing to
require that ACOs demonstrate patientcenteredness as required by the statute
by addressing all 8 areas outlined
previously. We also considered
confining the list of mandatory criteria
to only those items specifically
mentioned in section 1899(b)(2)(H) of
the Act that is, to ‘‘the use of patient and
caregiver assessments’’ and ‘‘the use of
individualized care plans.’’ However,
the statute clearly identifies these two
items only as examples of patientcenteredness, and specifies that an ACO
must be required to demonstrate that it
meets patient-centeredness criteria
‘‘specified by the Secretary.’’ Thus, we
believe the Secretary is required to
define and has discretion to specify
criteria in addition to the two criteria
that are specifically mentioned in the
statute.
We note there is substantial overlap
and alignment between these patient
centeredness criteria as defined by the
Secretary in accordance with section
1899(b)(2)(H) of the Act and the
processes ACOs are required to define
and documents they are required to
submit as discussed previously to fulfill
eligibility as outlined in section
1899(b)(2)(G) of the Act and
1899(b)(2)(F) of the Act. Therefore,
many of the ways an ACO defines
certain processes required by statute
may also serve to demonstrate it meets
patient centeredness criteria as defined
by the Secretary, thus reducing the
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burden for the ACO in meeting
eligibility requirements.
We are soliciting comment on
whether there are redundancies in the
list of the 8 criteria or other
considerations that might justify
narrowing the list. We are also
interested in whether the patient
centeredness criteria as defined by the
Secretary are sufficient to ensure that
ACOs participating in the Shared
Savings Program meet the eligibility
requirement to demonstrate patient
centeredness or whether there are
additional patient centeredness criteria
that should be added to our proposed
list in order to meet the goals of
improving the quality of health care
delivery and improving patient
satisfaction with their care.
Additionally, we seek comment on
whether these criteria are burdensome
and whether they might create
disincentives to participate or make it
difficult for small entities to participate
in the program.
Later in the document, we discuss 4
of the 8 criteria in detail and solicit
comment regarding (a) Implementation
of the beneficiary experience of care
survey; (b) beneficiary involvement in
governance; (c) identification of
population health needs and
consideration of diversity; and (d)
implementation of individualized care
plans and integration of community
resources.
a. Beneficiary Experience of Care Survey
As discussed previously, we propose
that ACOs have a beneficiary experience
of care survey in place and that the
ACO’s application should describe how
the ACO will use the survey results to
improve care over time. Surveys are
important tools for assessing beneficiary
experience of care and outcomes. As
part of the requirement to implement a
beneficiary experience of care survey,
we propose to require ACOs to collect
and report on measures of beneficiaries’
experience of care and we expect ACOs
to submit their plan on how they will
promote, assess, and continually
improve in weak areas identified by the
survey.
Many surveys are being used in both
the private and public sectors, including
the Medicare Health Outcomes Survey
used by Medicare Advantage (MA)
plans, Consumer Assessment of
Healthcare Providers and Systems
(CAHPS) survey tools, and Health
Resources Services Administration’s
(HRSA’s) Health Center Patient
Satisfaction Survey. We are proposing
that ACOs be required to use a specified
survey that assesses beneficiary
experience of care and functional status.
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As proposed in section II.E. of this
proposed rule, scoring on the patient
experience of care survey would become
part of the assessment of the ACOs
quality performance. Specifically, we
are proposing that ACOs be required to
use the Clinician and Group CAHPS
survey. We also propose to require
adoption of an appropriate functional
status survey module that may be
incorporated into the CAHPS survey.
The CAHPS Survey is a nationally
recognized survey, developed by the
Agency for Healthcare Research and
Quality (AHRQ), which is widely used
across the health care spectrum. The
survey is designed to standardized
patient questionnaires that can be used
to compare results across sponsors and
over time, which identifies the issues
that are salient to consumers and
influence their decisions. Since the
ACO must contain primary care ACO
professionals but otherwise has
flexibility to incorporate other types of
ACO participants, we believe the
Clinician and Group CAHPS Survey is
an appropriate tool to assess beneficiary
experience of care and functional status
in the ACO. Using this standard and
well established survey instrument, we
can more easily compare outcomes and
beneficiary satisfaction across ACOs, as
well as in certain modules in common
between ACOs and Medicare FFS and
MA plans. It would also help to ensure
that survey measures are adequate to
meet the program’s purposes and that
measures employed in the instrument
are valid and reliable. However, we
recognize that requiring the use of a
specific survey instrument would
increase the administrative burden of
the Shared Savings Program on ACOs
who are not currently using the
specified instrument. Accordingly, we
are soliciting comment on whether other
existing survey tools would be more
appropriate for ACO quality assessment.
We also considered proposing to
allow ACOs to continue using the
survey tools with which they are
already familiar or of their own
choosing at least in the initial stages of
the program. Allowing ACOs to employ
survey tools of their own choosing
would provide maximum flexibility for
ACOs, and would be least disruptive to
existing ACO initiatives to survey
beneficiary experience. However,
allowing ACOs to employ survey tools
of their own choosing would severely
impede our ability to compare
beneficiary experience across ACOs.
Moreover, in some instances, the
instruments selected by ACOs may use
measures that are insufficient to meet
the program’s purposes, or measures
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which are not valid and reliable. In
other instances, it might be that ACOs
using more comprehensive survey tools
would be unfairly penalized from the
perspective of the performance
standards in comparison to ACOs using
less extensive surveys.
b. Patient Involvement in Governance
Another of the proposed patientcentered criteria discussed previously is
the requirement that ACOs provide for
patient involvement in their governing
processes. We are proposing that, in
order to satisfy this criterion, ACOs will
be required to demonstrate a
partnership with Medicare FFS
beneficiaries by having representation
by a Medicare beneficiary serviced by
the ACO, in the ACO governing body.
We believe the best way to demonstrate
a patient-centered program is for
Medicare beneficiaries to have a voice
in the decision making process.
Although, there may be concerns or
differences in the ability of some ACOs
to include a beneficiary on the
governing board, given State laws, we
are seeking comment on the inclusion of
a Medicare beneficiary serviced by the
ACO on the governing body. In order to
safeguard against any conflicts of
interest, any patient(s) included in an
ACO’s governing body, or an immediate
family member, must not have any
conflict of interest, and they may not be
an ACO provider/supplier within the
ACO’s network.
We recognize that a requirement for
representation by a Medicare
beneficiary serviced by the ACO, on an
ACO’s governing body will not
necessarily guarantee outcomes that are
in line with the goals of the Shared
Savings Program in general or patientcentered criteria in particular. Medicare
beneficiary representation on an ACO’s
governing body may even be relatively
ineffectual if Medicare beneficiaries
hold relatively few seats on the
governing body. Furthermore, such a
requirement may pose difficulties for
ACOs that already have a governing
body and bylaws that do not require or
may even prohibit Medicare beneficiary
presence, and this requirement may
therefore reduce the number of ACOs
that participate in the Shared Savings
Program, at least in its initial stages.
However, we believe it is important to
the patient-centered orientation of the
Shared Savings Program to provide for
beneficiaries to have a voice in ACO
governance.
We considered proposing that, instead
of requiring direct Medicare beneficiary
representation on ACO governing
bodies, ACOs could demonstrate a
partnership with Medicare FFS
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beneficiaries by having a Medicare
beneficiary advisory committee or
panel. Such a proposal would also serve
to indicate the importance of beneficiary
engagement in the ACO’s activities to
improve the quality and efficiency of
health care services. It would also
provide ACOs with the opportunity to
form committees or panels that
represent the voices of all of their
patient types, including Medicare FFS
beneficiaries. In addition, a unified
advisory committee voice may, under
some circumstances at least, be more
effective than, a single beneficiary
representative in the ACO governing
body in advancing the goal of
beneficiary participation in ACO
governance. Furthermore, it would
avoid requiring existing ACO governing
bodies that do not currently have or
whose bylaws do not permit Medicare
beneficiary representation to revise their
bylaws or to forego participation in the
Shared Savings Program. However, a
pure advisory committee or panel may
be an inadequate conduit for Medicare
beneficiary participation in ACO
governance compared to their presence
on the actual decision-making body of
the ACO. Presence on the governing
body would provide beneficiaries with
an active role in the decision-making
process and thus give beneficiaries more
influence over the ACO’s activities. In
contrast, as an advisory committee or
panel member, the beneficiary’s voice
provides guidance on the Shared
Savings Program ACO’s decisionmaking without the benefit of more
active control over ACO activities.
Therefore, we are proposing that
ACOs be required to demonstrate a
partnership with Medicare FFS
beneficiaries and meet patient
centeredness criteria by including a
Medicare beneficiary serviced by the
ACO on the ACO governing body. We
are soliciting comment on whether the
requirement for beneficiary
participation should include a
minimum standard for such beneficiary
participation on ACO governing bodies
(for example, a minimum number of
beneficiaries, or a minimum proportion
of control over an ACO’s governing
body.). In addition, we are soliciting
comment on the possible role of a
Medicare beneficiary advisory panel or
committee in promoting the goal of
engaging patients in ACO governance.
In particular, we seek comment on
whether—(1) a Medicare beneficiary
advisory panel or committee would be
sufficient in and of itself in providing
for appropriate patient participation in
ACO governance; and (2) establishing
Medicare beneficiary advisory panels or
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committees should be required in
addition to requiring patient
representation on ACO governing
bodies.
We request comment on the proposal
to engage in partnership with Medicare
beneficiaries. We are specifically
interested in whether this requirement
will create disincentives for
participation among smaller entities.
c. Evaluation of Population Health
Needs and Consideration of Diversity
A third proposed patient-centered
criterion on which we are seeking
comments is the requirement that an
ACO has a process for evaluating the
health needs of the population,
including consideration of diversity in
its patient populations, and a plan to
address the needs of its populations.
Several institutions and associations
such as National Committee for Quality
Assurance (NCQA) and AHRQ have
made recommendations regarding
evaluation of population health and
diversity. For example, NCQA has
developed multicultural health care
standards and guidelines which include
requirements for collecting of patient
information that help the organization
understand the composition of the
population, providing culturally and
linguistically appropriate services, and
detecting health care disparities. Other
institutions and associations have
developed similar guidelines which
emphasize promoting cultural
sensitivity and addressing disparities
through provider/management
education and the translation of surveys
and health promoting literature
distributed by the provider into
languages relevant to the provider’s
population. Establishing partnerships
with a State or local health department
which performs community health
needs assessments and applying these
findings to the ACO’s population and
activities may be another viable option
for meeting this criterion.
Accordingly, we propose that, in
order to satisfy this patient-centered
criterion, ACOs would be required to
describe in their application their
process for evaluating the health needs
of their Medicare population, including
consideration of diversity, and a plan to
address the needs of their Medicare
population.
d. Implementation of Individualized
Care Plans and Integration of
Community Resources
Finally, we are proposing that ACOs
must have systems in place to identify
high-risk individuals and processes to
develop individualized care plans for
targeted patient populations. The plan
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must be tailored to—(1) The
beneficiary’s health and psychosocial
needs; (2) account for beneficiary
preferences and values; and (3) identify
community and other resources to
support the beneficiary in following the
plan. This plan would be voluntary for
the beneficiary, privacy protected, and
would not be shared with Medicare or
the ACO governing body; it would
solely be used by the patient and ACO
providers/suppliers for care
coordination. If applicable, and the
beneficiary consents, the care plan
should be shared with the caregiver,
family, and others involved in the
beneficiary’s care. We propose that an
ACO would be required to have a
process in place for developing,
updating, and, as appropriate, sharing
the beneficiary care plan with others
involved in the beneficiary’s care, and
providing it in a format that is
actionable by the beneficiary.
We are requesting comments on our
proposal that ACOs be required to
demonstrate use of individualized care
plans for targeted beneficiary
populations in order to be eligible for
the Shared Savings Program. In order to
satisfy this requirement fully, we
propose that the development of such
individualized care plans must grow
from adherence of a related patientcenteredness criterion, that is, their
development should be a result of
shared decision-making which fully
engages beneficiaries and their families,
taking into account their values and
preferences in developing a unique plan
of care for each individual.
The individualized care plans should
include identification of community
and other resources to support the
beneficiary in following the plan. To
this end, we believe that a process for
integrating community resources into
the ACO is an important part of patient
centeredness. A wide variety of
organizations, although not necessarily
ACO participants, may be considered a
community resource, including:
Employers, commercial health plans,
local businesses, State/local government
agencies, local quality improvement
organizations or collaboratives (such as
health information exchanges).
Collaboration with these types of
community resources can be an
important part of enabling ACOs to take
account of the entirety of Medicare
beneficiary population’s needs relative
to their environment. Community
stakeholder engagement in an ACO
could be explicitly incorporated via
community representation on the
governing body, by having a community
representative on an advisory board, or
by other innovative mechanisms.
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Individualized plans of care are not
only an integral part of providing
quality health care to both high-risk
patients or patients with multiple
chronic conditions, but are equally
important in proactively maintaining
the health for any beneficiary. For
purposes of the application to
participate in the Shared Savings
Program, we propose that an ACO
would be required to submit a
description of its individualized care
program, along with a sample care plan,
and explain how this program is used to
promote improved outcomes for, at a
minimum, their high-risk and multiple
chronic condition patients. In addition,
the ACO should describe additional
target populations that would benefit
from individualized care plans. We also
propose that ACOs be required to
describe how they will partner with
community stakeholders as part of their
application. ACOs that have a
stakeholder organization serving on
their governing body would be deemed
to have satisfied this requirement. We
request comment on these proposals.
We are specifically interested in
whether these requirements will create
disincentives for participation among
smaller entities.
11. ACO Marketing Guidelines
We believe there is a potential for
beneficiaries to be misled about
Medicare services available from an
ACO or about the providers and
suppliers from whom they can receive
those services. We realize that care
coordination is an important component
of the Shared Savings Program;
however, the potential for shared
savings may be an incentive for ACOs,
ACO participants, or ACO providers/
suppliers to engage in behavior that may
confuse or mislead beneficiaries about
the Shared Savings Program or their
Medicare rights. For example, although
it is expected that ACO providers/
suppliers participating in an ACO will
refer patients to other ACO providers/
suppliers in the ACO, we are concerned
that beneficiaries may be misled into
thinking the ACO is similar to a
managed care organization, and that
they may only receive services or only
certain services from the other
participating ACO providers/suppliers.
Although section 1899 of the Act is
silent with regard to marketing activities
and other forms of beneficiary
communications by ACOs, section
1899(b)(2)(H) of the Act requires an
ACO to demonstrate ‘‘that it meets
patient-centeredness criteria.’’ We
believe that in order to be truly patientcentered, an ACO must not only provide
care coordination that is tailored to the
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needs of the individual beneficiary, but
also avoid engaging in activities that
may prevent its assigned beneficiaries
from taking advantage of the full range
of benefits to which they are entitled
under the Medicare FFS program,
including the right to choose between
healthcare providers and care settings.
As a result, issuing beneficiary
communications or engaging in
marketing activities that may be
confusing or misleading would not be
patient-centered because these activities
restrict the ability of beneficiaries and/
or their caregivers to be informed about
their health care choices and thus limit
the opportunity for beneficiaries to be
properly involved in the management of
their own care.
Accordingly, we think it would be
appropriate and consistent with the
purpose and intent of the statute to limit
and monitor the use of beneficiary
communications specifically related to
the ACO operations or functions as well
as ACO marketing activities and
materials by ACOs to ensure that such
communications and marketing by
ACOs are used only for appropriate
purposes, such as notification that a
beneficiary’s healthcare provider is
participating in the ACO, issuance of
any CMS required notices, notification
of provider or ACO terminations. This
policy will protect Medicare
beneficiaries by minimizing the
potential that they will be misled or
confused by ACO marketing.
Additionally, the policy is consistent
with marketing provisions used in other
Medicare programs such as MA.
We are proposing that all ACO
marketing materials, communications,
and activities related to the ACO and its
participation in the Shared Savings
Program, such as mailings, telephone
calls or community events, that are used
to educate, solicit, notify, or contact
Medicare beneficiaries or providers/
suppliers regarding the ACO and its
participation in the Shared Savings
Program, be approved by us before use
to protect beneficiaries and to ensure
that they are not confusing or
misleading. This requirement would
also apply to any materials or activities
used by ACO participants or ACO
providers/suppliers on behalf of the
ACO to communicate about the ACO’s
participation in the Shared Savings
Program in any manner to Medicare
beneficiaries. In addition, we would
want to ensure that materials distributed
to beneficiaries do not misrepresent
Shared Savings Program policies or
suggest that we endorse the ACO, its
ACO participants, or its ACO providers/
suppliers.
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We are further proposing that before
any changes can be made to any
approved materials, the revised
materials must be approved by us before
use. Finally, because the failure to
comply with these requirements would
demonstrate that the ACO does not meet
the patient-centeredness criteria and
therefore may no longer be eligible to
participate in the program, we propose
that an ACO that fails to adhere to these
requirements may be placed under a
corrective action plan or terminated, at
our discretion.
For purposes of the Shared Savings
Program, we are proposing to define
ACO marketing materials,
communications, and activities as
including, but not limited to, general
audience materials such as brochures,
advertisements, outreach events, letters
to beneficiaries, web pages, mailings, or
other activities, conducted by or on
behalf of the ACO, or by ACO
participants, or ACO providers/
suppliers participating in the ACO, or
by other individuals on behalf of the
ACO or its participating providers and
suppliers. If these materials or activities
are used to educate, solicit, notify, or
contact Medicare beneficiaries or
providers and suppliers regarding the
ACO and its participation in the Shared
Savings Program, they must be
approved by us.
We do not believe that the following
materials and activities would be
subject to our approval: Beneficiary
communications that are informational
materials, that are customized or limited
to a subset of beneficiaries; and
materials that do not include
information about the ACO or providers
in the ACO; materials that cover
beneficiary-specific billing and claims
issues or other specific individual
health related issues; and educational
information on specific medical
conditions, (for example, flu shot
reminders), or referrals, for example, as
discussed in section II. C. of this
proposed rule, exceptions to the
definition of ‘‘marketing’’ under the
HIPAA Privacy Rule.
12. Program Integrity Requirements
Section 1899(a)(1)(A) of the Act
authorizes the Secretary to specify
criteria that ACO participants must meet
in order to work together to manage and
coordinate care for Medicare FFS
beneficiaries through an ACO. Using
this authority, we propose several
program integrity criteria to protect the
Shared Savings Program from fraud and
abuse and to ensure that the Shared
Savings Program does not become a
vehicle for, or increase the potential for,
fraud and abuse in other parts of the
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Medicare program or in other Federal
health care programs.
a. Compliance Plans
We are proposing that an ACO must
have a compliance plan that addresses
how the ACO will comply with
applicable legal requirements. We
recognize that the specific design and
structure of an effective compliance
plan may vary depending on the size
and business structure of the ACO. We
are proposing that the ACO demonstrate
that it has a compliance plan that
includes at least the following elements,
which are common in the compliance
industry: A designated compliance
official or individual who is not legal
counsel to the ACO and who reports
directly to the ACO’s governing body;
mechanisms for identifying and
addressing compliance problems related
to the ACO’s operations and
performance; a method for employees or
contractors of the ACO or ACO
providers/suppliers to report suspected
problems related to the ACO;
compliance training of the ACO’s
employees and contractors; and a
requirement to report suspected
violations of law to an appropriate law
enforcement agency. Nothing in this
rule would prevent an ACO from using
or building on an existing compliance
program, if it has one (or if its ACO
participants have programs that can be
incorporated). To achieve an effective
compliance program, an ACO may also
want to consider coordinating its
compliance efforts with existing
compliance efforts of its ACO providers/
suppliers. It is not our intention that an
ACO would need to engage in
duplicative efforts to meet the
compliance program requirement. The
goal is for ACOs to have effective
compliance mechanisms.
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b. Compliance With Program
Requirements
We propose that, notwithstanding any
relationships that the ACO may have
with other entities related to ACO
activities, the ACO maintains ultimate
responsibility for compliance with all
terms and conditions of its agreement
with us. We propose to require that all
contracts or arrangements between or
among the ACO, its ACO participants
and ACO providers/suppliers, and other
entities furnishing services related to
ACO activities require compliance with
the obligations under the 3-year
agreement, including the document
retention and access requirements
discussed in section II.H of this
proposed rule. We solicit comments on
our proposal.
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We must ensure the accuracy,
completeness, and truthfulness of
information submitted to us to
determine an organization’s eligibility to
participate in the Shared Savings
Program as an ACO, its compliance with
program requirements, its eligibility for
shared savings payments, and the
amount of any payments owed to or by
the ACO. To that end, we propose that
an authorized representative of the
ACO—specifically, an executive who
has the ability to legally bind the ACO—
must certify the accuracy, completeness,
and truthfulness of information
contained in its Shared Savings Program
application, 3-year agreement, and
submissions of quality data and other
information. The certification must be
made at the time the application,
agreement, and information is
submitted.
We further propose that, as a
condition of receiving a shared savings
payment, an authorized representative
with authority to legally bind the ACO
must make a written request to us for
payment of the shared savings in a
document that certifies the ACO’s
compliance with program requirements
as well as the accuracy, completeness,
and truthfulness of any information
submitted by the ACO the ACO
participants, or the ACO providers/
suppliers to us, including any quality
data or other information or data relied
upon by us in determining the ACO’s
eligibility for, and the amount of, a
shared savings payment or the amount
owed by the ACO to us. We further
propose that, if such data are generated
by ACO participants or another
individual or entity, or a contractor, or
subcontractor of the ACO or the ACO
participants, such ACO participant,
individual, entity, contractor, or
subcontractor must similarly certify the
accuracy, completeness, and
truthfulness of the data and provide the
government with access to such data for
audit, evaluation, and inspection.
c. Conflicts of Interest
We are proposing that the ACO
governing body have a conflicts of
interest policy that applies to members
of the governing body. The purpose of
this proposal is to ensure that members
of the governing body act in the best
interests of the ACO and Medicare
beneficiaries We propose that the
conflicts of interest policy must require
members of the governing body to
disclose relevant financial interests.
Further, the policy must provide a
procedure for the ACO to determine
whether a conflict of interest exists and
set forth a process to address any
conflicts that arise. Such a policy would
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also address remedial action for
members of the governing body that fail
to comply with the policy. We solicit
comments on this proposal, including
the scope and content of such a policy.
d. Screening of ACO Applicants
The Medicare program includes
substantial screens of enrolling
providers and suppliers, including, for
example, newly enrolling ACO
participants. ACOs will not be subject to
those existing screens because they are
not enrolling in Medicare. Consistent
with our efforts throughout the
Medicare program to strengthen
provider enrollment standards and
encourage compliance with program
requirements, we are considering
screening ACOs during the Shared
Savings Program application process
with regard to their program integrity
history, including any history of
program exclusions or other sanctions
and affiliations with individuals or
entities that have a history of program
integrity issues. ACOs whose screening
reveals a history of program integrity
issues and/or affiliations with
individuals or entities that have a
history of program integrity issues may
be subject to rejection of their Shared
Savings Program applications or the
imposition of additional safeguards or
assurances against program integrity
risks. We solicit comments on the
nature and extent of such screening and
the screening results that would justify
rejection of an application or increased
scrutiny.
e. Prohibition on Certain Required
Referrals and Cost-Shifting
In section II.D. of this proposed rule,
we propose to assign beneficiaries to an
ACO after the conclusion of a
performance period, but we also
indicate that we are considering
assigning beneficiaries to an ACO on a
prospective basis at the beginning of a
performance period. We are concerned
that ACOs or ACO participants may
offer or be offered inducements to
overutilize services or to otherwise
increase costs for Medicare or other
Federal health care programs with
respect to the care of individuals who
are not assigned to the ACO under the
Shared Savings Program. The risk of
such abuse might be heightened if the
final rule provides for prospective
assignment of beneficiaries. To address
the risk of inappropriate cost-shifting
within Medicare and other Federal
health care programs, we are
considering prohibiting ACOs and their
ACO participants from conditioning
participation in the ACO on referrals of
Federal health care program business
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that the ACO or its ACO participants
know or should know is being provided
to beneficiaries who are not assigned to
the ACO.
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C. Establishing the 3-Year Agreement
With the Secretary
1. Options for Start Date of the
Performance Year
Section 1899 (b)(2)(B) of the Act, as
added by section 3022 of the Affordable
Care Act provides that an ‘‘ACO shall
enter into an agreement with the
Secretary to participate in the [Shared
Savings Program] for no less than a 3year period * * * ’’ In establishing the
requirement for a minimum 3-year
agreement period, the statute does not
prescribe a particular application period
or specify a start date for ACO
agreements. In this section of this
proposed rule, we will discuss our
proposals for establishing an application
period and for setting the start date for
the 3-year agreements with ACOs.
We considered several options for
establishing start dates, with the
corresponding 3-year agreement
periods: Annual start dates; semiannual
start dates; rolling start dates; and
delayed start dates. In our consideration
of these options, we attempted to
balance the need for maximum
flexibility for program applicants with
the advantages of establishing a
streamlined administrative approach.
Adopting an annual application period
and start date would create cohorts of
ACO applicants, which would be
simultaneously evaluated for eligibility
to participate in the program.
Agreements with ACOs of the same
cohort would take effect on the same
date each year. This would allow for
more streamlined processes around
agreement renewal and performance
analysis, evaluation and monitoring.
However, under section 1899(a)(1) of
the Act, the Secretary must establish the
Shared Savings Program by not later
than January 1, 2012. Given the short
timeframe for implementation of the
program and our desire to permit as
many qualified ACOs as possible to
participate in the first year, we also gave
a great deal of consideration to
alternative approaches that would
provide flexibility to program
applicants. For instance, we could allow
ACOs to apply on a ‘‘rolling’’ basis in
which applications are accepted and
evaluated any time of year and the
ACO’s agreement period would begin
after a determination that the eligibility
requirements had been met. In this way,
applicants could apply throughout the
course of the year as they become ready
and we could review and approve
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applications and begin performance
periods on a rolling basis.
After exploring the various
alternatives, it has become clear that the
greatest barrier to any option other than
an annual uniform start date relates to
appropriate beneficiary assignment,
particularly for markets where there
may be multiple ACOs. First, if ACO
agreements begin more often than once
a year, beneficiaries could be assigned
to two ACOs for an overlapping period.
As discussed in section II.D. of this
proposed rule, we propose that
beneficiaries will be assigned to ACOs
based upon where they receive the
plurality of their primary care services.
Since the physician associated with the
plurality of a beneficiary’s primary care
services could vary from year to year,
having multiple start dates could result
in a beneficiary being assigned to
multiple ACOs for an overlapping
period. This scenario would result in
confusion for beneficiaries and the
potential for duplicate shared savings
payments for care provided to a single
beneficiary. Problems with patient
assignment may cause unintended
consequences for per capita costs,
making it difficult to make comparisons
of one ACO’s performance to another
that has a different start date. In
addition, adopting multiple start dates
within a year would require multiple
cycles for application review and
approval, calculation of baselines and
targets, data sharing, quality reporting,
and financial reconciliation, which
would impose a significant
administrative challenge.
After evaluating the various options
for start date, we are proposing to
establish an application process with an
annual application period during which
a cohort of ACOs would be evaluated for
eligibility to participate in the Shared
Savings Program. We further propose
that the performance years be based on
the calendar year to be consistent with
most CMS payment and quality
incentive program cycles. In other
words, we propose: (1) To adopt the
general requirement that ACO
applications must be submitted by a
deadline established by us; (2) we will
review the applications and approve
applications from eligible organizations
prior to the end of the calendar year; (3)
the requisite 3-year agreement period
will begin on the January 1 following
approval of an application; and (4) the
ACO’s performance periods under the
agreement will begin on January 1 of
each respective year during the
agreement period.
However, we are concerned that, in
light of the short time frame for
implementing the Shared Savings
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Program in the first year of the program,
a January 1 start date might not provide
the flexibility necessary to allow all
interested ACOs to complete their
application packages. Accordingly, we
solicit comment on any alternatives to a
January 1 start date that would allow the
greatest number of qualified
organizations to apply to participate in
the first year of the program. One
specific example of an alternative to a
single start date of January 1 for the first
year of the Shared Savings Program
might be to add an additional start date
of July 1 and to allow the agreement
period for ACOs with a July 1 start date
to be increased to 3.5 years. Under this
example, the first performance year of
the agreement period would be defined
as 18 months in order that all of the
agreement periods would synchronize
with ACOs entering the program on
January 1 of the following year. We
envision that if adopted, this alternative
would only be available in the first year
of the program and for all subsequent
years all applications would have to be
reviewed and accepted prior to the
beginning of the applicable calendar
year and all agreements would be for 3
years.
2. Timing and Process for Evaluating
Shared Savings
Section 1899(d)(1) of the Act, as
added by section 3022 of the Affordable
Care Act, provides that an ACO shall be
eligible to receive shared savings
payments for each year of the agreement
period, if the ACO has met the quality
performance standards established
under section 1899(b)(3) of the Act and
has achieved the required percent of
savings below its benchmark. However,
the statute is silent with respect to when
the shared savings determination should
be made. Potential ACOs have indicated
that they need timely feedback on their
performance in order to develop and
implement improvements in care
delivery. In developing our proposals,
we have therefore been attentive to the
importance of determining shared
savings payments and providing
feedback to ACOs on their performance
in a timely manner while at the same
time not sacrificing the accuracy needed
to calculate per capita expenditures.
Our determination of an ACO’s
eligibility to receive a payment for
shared savings will be based upon an
analysis of the claims submitted by
providers and suppliers for services and
supplies furnished to beneficiaries
assigned to the ACO. There is an
inherent lag between when a service is
performed and when a claim is
submitted to us for payment.
Additionally, there is also a time lag
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between when the claim is received by
us and when the claim is paid. For this
reason, all Medicare service and
expenditure data have what can be
defined as a claims run-out period. The
claims run-out period is the time
between when a Medicare-covered
service has been furnished to a
beneficiary and when the final payment
is actually issued for the respective
service.
From the perspective of the utilization
and expenditure data that would be
needed in order to determine an ACO’s
eligibility to receive shared savings and
to provide performance feedback
reports, the longer the claim run-out
period, the more complete and accurate
the utilization and expenditure data
would be for any given year. Higher
completion percentages are associated
with longer run out periods and thus
would necessitate a longer delay before
we could determine whether an ACO is
eligible to receive shared savings and
provide performance feedback.
Conversely, a lower completion
percentage would be associated with a
shorter run out period and thus a
quicker turnaround for the shared
savings determination and for the
provision of performance feedback.
Based upon historical trends, a 3-month
run-out would result in a completion
percentage of approximately 98.5
percent for physician services and 98
percent for Part A services. A 6-month
run-out of claims data results in a
completion percentage of approximately
99.5 percent for physician services and
99 percent for Part A services. Since
neither a 3-month nor a 6-month runout of claims data would offer complete
calendar year utilization and
expenditure data, we would have to
work with our Office of the Actuary to
determine if the calculation of a
completion percentage is warranted. If
determined necessary, the completion
percentage would be applied to ensure
that the shared savings determination
reflects the full costs of care furnished
to assigned beneficiaries during a given
calendar year. Thus, we must balance
the need to ensure accurate and
complete claims data are used to
determine shared savings with the need
to provide timely feedback to ACOs
participating in the Shared Savings
Program. Additionally, regardless of
whether we use a 3-month or 6-month
claims run-out period, we are concerned
that some claims (for example, high cost
claims) may be filed after the claims
run-out period which would affect the
accuracy of the amount of the shared
savings payment. We are considering,
and seek comment on, ways to address
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this issue, including applying an
adjustment factor determined by CMS
actuaries to account for incomplete
claims, termination of the ACO’s
agreement with us for ACOs found to be
holding claims back, or attributing
claims submitted after the run-out
period to the following performance
period.
We propose using a 6-month claims
run-out to calculate the benchmark and
per capita expenditures for the
performance year. A 6-month claims
run-out will allow us to more accurately
determine the per capita expenditures
associated with each respective ACO.
Although the use of a 6-month claims
run out will delay the computation of
shared savings payments and the
provision of feedback to participating
ACOs, the trade-off for a more accurate
calculation of per capita costs is
warranted. More accurately defining the
per capita expenditures will allow us to
share the appropriate amount of savings
or alternatively, if no shared savings are
realized, it will allow the ACO to focus
on potential areas for improvement.
However, we seek comment on whether
there are additional considerations that
might make a 3-month claims run-out
more appropriate.
3. Data Sharing
Under section 1899(b)(2)(A) of the
Act, as added by section 3022 of the
Affordable Care Act, an ACO must, ‘‘be
willing to become accountable for the
quality, cost, and overall care of the
Medicare fee-for-service beneficiaries
assigned to it.’’ Section 1899 of the Act
does not address what data, if any, we
should make available to ACOs on their
assigned beneficiary populations to
support them in evaluating the
performance of ACO participants and
ACO providers/suppliers, conducting
quality assessment and improvement
activities, and conducting populationbased activities relating to improved
health. In agreeing to become
accountable for a group of Medicare
beneficiaries, we generally expect that
participating ACOs are able to, or are
working toward, independently
identifying and producing the data they
believe are necessary to best evaluate
the health needs of their patient
population, improve health outcomes,
monitor provider/supplier quality of
care and patient experience of care, and
produce efficiencies in utilization of
services. Moreover, this ability to selfmanage is a critical skill for each ACO
to develop, leading to an understanding
of the unique patient population that it
serves.
However, we also recognize that
while an ACO typically should have, or
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is moving toward having, complete
information for the services it provides
to or coordinates on behalf of its FFS
beneficiary population, it may not have
complete information on a FFS
beneficiary who, for example, has
chosen to receive services, medications
or supplies from providers of services
and suppliers outside its organization.
We believe that providing ACOs with an
opportunity to request CMS claims data,
as described later in this proposed rule,
on their potentially assigned beneficiary
population would allow them to
understand the totality of care provided
to beneficiaries assigned to them by
identifying the services and supplies
that fee-for-service beneficiaries receive
during the performance year both
within and outside of the ACO. We
believe that access to this data would
promote coordinated care and a better
understanding of the population served
by the ACO with resulting positive
impacts on both the quality and
efficiency of ease of delivered. ACOs
represent a positive step toward
transforming the current health care
system and we want to ensure that
participating organizations have access
to information that will assist them in
achieving both improvements in the
quality of care and a better
understanding of the population served
by the ACO while simultaneously
lowering the growth in health care costs.
We could provide data to ACOs in
different forms with a focus on different
levels of information, for example,
aggregated population level data or
beneficiary identifiable data. These data
could be combined with data collected
within the ACO. For example, our data
could be combined with provider level
data compiled within the ACO.
Combining aggregate and beneficiary
identifiable data as well as provider
level and other internally generated data
would provide ACOs with a more
complete picture about the care their
assigned beneficiaries receive both
within and outside the ACO, their ACO
participants and ACO providers/
suppliers’ patterns of care, and could be
used to assess their performance relative
to their previous years’ performance.
With this information, in accordance
with established privacy and security
protections, ACOs would be able to
identify how its ACO participants and
ACO providers/suppliers measure up to
benchmarks and targets, how they
perform in relation to peers internally,
and identify which categories of
beneficiaries would benefit most from
care coordination and other patientcentered approaches. For a more
complete discussion of the requirements
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associated with the sharing of internally
generated data, please see section II.B.
of this proposed rule
4. Sharing Aggregate Data
Because we believe that ACOs have
the potential to significantly improve
the quality of care provided to Medicare
beneficiaries while improving the
efficiency and cost-effectiveness of that
care, we believe that, where feasible, we
should provide information to help
ACOs improve the quality of care,
improve the health of their beneficiary
population, and create efficiencies
within their systems. One possible
approach is to provide aggregated data
on beneficiary use of health care
services. An ACO should be able to use
aggregated data reports on its assigned
or potentially assigned beneficiary
population to monitor, understand, and
manage its utilization and expenditure
patterns as well as to develop, target,
and implement quality improvement
programs and initiatives. For example, if
data shows that an ACO’s beneficiary
population had a high rate of hospital
readmissions, the ACO could consider
the need for actions to improve
discharge coordination among its
attending physicians, hospitals, and
post-acute care providers or to improve
access to primary care clinics. Similarly,
an analysis of aggregated Part D data
that shows beneficiaries were not filling
their prescriptions could lead to
interventions applicable to all
beneficiaries designed to assess and
develop strategies to overcome
difficulties in filling prescriptions.
Likewise, aggregated data could show a
relatively high incidence within the
ACO’s beneficiary population of certain
types of procedures relative to national
benchmarks, potentially prompting an
ACO to further explore and examine the
appropriateness of its ACO participants’
and ACO providers/suppliers’ practice
patterns by using provider-level data.
In the PGP demonstration, we
provided several types of aggregate data
to the participating group practices. We
generated an annual profile report that
provided the following information:
• Financial performance including
number of patients seen, number of
patients assigned, per capita
expenditures, risk score, benchmark,
total assigned beneficiary expenditures,
minimum savings amount, shareable
savings, and annual performance
payment.
• Quality performance scores,
including numerator, denominator, and
rate for each measure along with the
target benchmark for each measure.
• Aggregated metrics on the assigned
beneficiary population, including a
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breakdown of the population into high
risk score beneficiaries, beneficiaries
with 1 or more hospitalizations, and
chronic disease subpopulations such as
patients with congestive heart failure,
coronary artery disease, hypertension,
chronic obstructive pulmonary disease,
and diabetes.
• The number of patients overall and
in each subpopulation with emergency
department visits, hospital discharges,
physician visits and their corresponding
rate for the assigned population.
The feedback received on the PGP
demonstration suggested that making
these data available was helpful to the
participating practices; they noted the
benefits of having aggregate data that
were more easily digestible compared to
‘‘data dumps’’ comprised of claimsbased data.
In general, by making similar types of
aggregate, data available to ACOs
participating in the Shared Savings
Program, we believe ACOs would have
a more complete picture of the services
rendered to their assigned FFS
beneficiaries, which would allow the
pursuit of a variety of strategies to
streamline and consolidate care
provision in a way that enhances quality
and slows the growth in Medicare
expenditures for their assigned
beneficiary population. Thus, providing
aggregated Medicare data reports to
ACOs in the beginning of the program
may be especially helpful to ACOs as
they identify priority areas of care upon
which to focus. Accordingly, similar to
the PGP demonstration, we propose to
provide aggregate data reports which
would include, when available,
aggregated metrics on the assigned
beneficiary population, and beneficiary
utilization data at the start of the
agreement period based on historical
data used to calculate the benchmark.
We further propose to include these
data in conjunction with the yearly
financial and quality performance
reports. Additionally, we propose to
provide quarterly aggregate data reports
to ACOs based upon the most recent 12
months of data from potentially
assigned beneficiaries. We request
comments on these proposals as well as
the kinds of aggregate data and
frequency of data reports that would be
most helpful to the ACO’s efforts in
coordinating care, improving health,
and producing efficiencies.
5. Identification of Historically Assigned
Beneficiaries
Based upon feedback from the PGP
demonstration, the RFI comments on
the Shared Savings Program, and Shared
Savings Program Open Door Forums, we
propose to make certain limited
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beneficiary identifiable data available at
the beginning of the first performance
year. In addition to sharing aggregated
data reports based on the ACO’s
historically assigned beneficiary
population, we believe the ACO would
benefit from understanding which of
their fee-for-service beneficiaries were
used to generate the aggregated data
reports. Accordingly, we propose to
disclose the name, date of birth (DOB),
sex and Health Insurance Claim Number
(HIC) of the historically assigned
beneficiary population. We believe that
knowing these identifiers would be
useful to the ACO in two ways: First,
the ACO providers could use the
information to identify the beneficiaries,
review their records, and identify care
processes that may need to change. For
example, the ACO might look at
whether an inability to get a timely
clinic appointment resulted in an
avoidable emergency room visit for a
particular patient. Second, experience
with the PGP demonstration has
suggested that a high percentage of
historically assigned patients will
continue to receive care from the ACO
participants and ACO providers/
suppliers. Knowing individuals who
have been assigned in the past would
help the ACO participants to identify
individuals who may benefit from
improved care coordination strategies
going forward.
Providing a list of historically
assigned patients to the ACO may also
raise concerns. In section II.D. of this
proposed rule, we have proposed to
assign beneficiaries to the ACO
retrospectively. One reason for this is
that we believe that the ACO should be
evaluated on the quality and cost of care
furnished to those beneficiaries who
actually chose to receive care from ACO
participants during the course of each
performance year. Another reason for
retrospective assignment is to encourage
the ACO to redesign its care processes
for all Medicare FFS beneficiaries, not
just for the subset of beneficiaries upon
whom the ACO is being evaluated. We
recognize that providing a list of
historically assigned beneficiaries may
provide an opportunity for the ACO to
identify and avoid at-risk beneficiaries
that appear on the list so that the costs
of these beneficiaries do not appear in
the calculation of the ACO’s actual
expenditures during a performance year.
We are addressing this concern through
the proposal described in section II.H. of
this proposed rule, that takes steps to
ensure ACOs do not avoid at-risk
beneficiaries.
Furthermore, we recognize that there
are a number of issues and sensitivities
surrounding the disclosure of
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individually-identifiable (patientspecific) health information, and note
that a number of laws place constraints
on the sharing of individually
identifiable health information. For
example, section 1106 of the Act
generally bars the disclosure of
information collected under the Act
without consent unless a law (statute or
regulation) permits for the disclosure. In
this instance, the HIPAA Privacy Rule
permits that legal authority and
provides for this proposed disclosure of
individually identifiable health
information by us.
Under the HIPAA Privacy Rule,
covered entities (defined as health care
plans, providers that conduct covered
transactions, and health care
clearinghouses) are barred from using or
disclosing individually identifiable
health information (called ‘‘protected
health information’’ or PHI) in a manner
that is not explicitly permitted or
required under the HIPAA Privacy Rule.
When another entity conducts a
function or activity involving the use or
disclosure of individually identifiable
health information on behalf of a
covered entity, that entity is a business
associate of the covered entity. (45 CFR
160.103). Under the HIPAA Privacy
Rule, a covered entity may disclose PHI
to business associates if it obtains
‘‘satisfactory assurances that the
business associate will appropriately
safeguard the information’’ (45 CFR
164.502(e)). These satisfactory
assurances generally take the form of
contractual obligations to protect the
data as the covered entity is required to
do under the HIPAA Privacy Rule. Any
use or disclosure of PHI that a covered
entity can make under the HIPAA
Privacy Rule can also be performed on
its behalf by a business associate if the
use or disclosure is authorized in the
contract between the covered entity and
the business associate.
The Medicare FFS program, a ‘‘health
plan’’ function of the Department, is
subject to the HIPAA Privacy Rule
limitations on the disclosure of PHI. The
ACO participants and ACO providers/
suppliers are also covered entities,
provided they are health care providers
as defined by 45 CFR 160.103 and they
or their agents electronically engage in
one or more HIPAA standard
transactions, such as for claims,
eligibility or enrollment transactions.
Similarly, an ACO may itself be a
HIPAA covered entity if it is a health
care provider that conducts such
transactions. Alternatively, based on
their work on behalf of ACO
participants and ACO providers/
suppliers in conducting quality
assessment and improvement activities,
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the ACOs will qualify as the business
associates of their covered entity ACO
participants and ACO providers/
suppliers.
In light of these relationships, the
proposed disclosure of the four
identifiers would be permitted by the
HIPAA Privacy Rule under the
provisions that permit disclosures of
PHI for ‘‘health care operations’’
purposes. Under those provisions, a
covered entity is permitted to disclose
PHI to another covered entity for the
recipient’s health care operations
purposes if both covered entities have or
had a relationship with the subject of
the PHI to be disclosed (which is true
here), the PHI pertains to that
relationship (which is also true here)
and the recipient will use the PHI for a
‘‘health care operations’’ function that
falls within the first two paragraphs of
the definition of ‘‘health care
operations’’ in the HIPAA Privacy Rule.
(45 CFR 164.506(c)(4)). The first
paragraph of the definition of health
care operations includes ‘‘populationbased activities relating to improving
health or reducing health costs, protocol
development, case management and
care coordination’’ (45 CFR 164.501). We
believe that this provision is extensive
enough to cover the uses we would
expect an ACO to make of the
identifying data elements for the
historically assigned patients. In coming
to this conclusion, we recognize that an
individual’s authorization is generally
required before using or disclosing PHI
for marketing purposes, 45 CFR 164.508,
but we also note that both those ACOs
acting as a covered entity (as opposed to
business associates) and those ACOs
acting on behalf of covered entity ACO
participants and ACO providers/
suppliers as business associates will be
able to use the four data elements to
communicate with individuals on the
list to describe available services and for
case management and care coordination
purposes under the exceptions to the
definition of ‘‘marketing’’ under the
HIPAA Privacy Rule, 45 CFR 164.501.
Furthermore, when using or
disclosing PHI, or when requesting this
information from another covered
entity, covered entities must make
‘‘reasonable efforts to limit’’ the
information that is used, disclosed or
requested the ‘‘minimum necessary’’ to
accomplish the intended purpose of the
use, disclosure or request, 45 CFR
164.502(b). We believe that the
provision of the four proposed data
elements would constitute the
minimum data necessary to accomplish
the Shared Savings Program goals of the
ACO.
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The Privacy Act of 1974 also places
limits on agency data disclosures. The
Privacy Act is a Federal withholding
statute. It applies when the Federal
government maintains a system of
records by which information about
individuals is retrieved by use of the
individual’s personal identifiers (names,
Social Security numbers, or any other
codes or identifiers that are assigned to
the individual). The Privacy Act
generally prohibits disclosure of
information from a system of records to
any third party without the prior written
consent of the individual to whom the
records apply, 5 U.S.C. 552a(b).
‘‘Routine uses’’ are an exception to this
general principle. A routine use is a
disclosure outside of the agency that is
compatible with the purpose for which
the data was collected. Routine uses are
established by means of a publication in
the Federal Register about the
applicable system of records describing
to whom the disclosure will be made
and the purpose for the disclosure. We
believe that the proposed data
disclosures are consistent with the
purpose for which the data discussed in
this rule was collected, and thus, should
not run afoul of the Privacy Act,
provided we ensure that an appropriate
Privacy Act system of records ‘‘routine
use’’ is in place prior to making any
disclosures.
Therefore, at the beginning of the
agreement period, at the request of the
ACO, we are proposing to provide the
ACO with a list of beneficiary names,
date of birth, sex, and HICN derived
from the assignment algorithm used to
generate the 3-year benchmark. As
discussed in section II.B. of this
proposed rule, these are beneficiaries
who received the plurality of primary
care services from primary care
physicians who are ACO participants.
We seek comment on this proposal and
on whether and how this information
would be beneficial to the goals of
improved care coordination and
improving care delivery for the ACO’s
assigned beneficiary population.
6. Sharing Beneficiary-Identifiable
Claims Data
While the availability of aggregate
beneficiary information and the
identification of the beneficiaries used
to determine the benchmark should
assist ACOs in the overall redesign of
care processes and coordination of care
for their assigned beneficiary
populations, we believe that more
complete beneficiary-identifiable
information would enable practitioners
in an ACO to better coordinate and
target care strategies towards the
individual beneficiaries who may
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ultimately be assigned to them. For
example, knowing which beneficiaries
have frequent emergency department
visits could help the ACO develop
systems to ensure these beneficiaries
have timely access to office-based care.
The PGP demonstration provided
beneficiary identifiable claims data to
the participating sites but the
beneficiary identifiable claims data that
was provided was the previous year’s
historical data on those beneficiaries
that might be assigned to the site. The
feedback we received from the PGP
demonstration was that the historical
beneficiary identifiable claims data was
useful in some instances but that
current year beneficiary claims data
would be preferred and result in a more
proactive approach to coordinating care.
Through comments on the November
17, 2010 RFI, open door forums, and
other venues, stakeholders have
expressed the importance of timely data
on their patient population. They
submit that they will need detailed data
for their patients so they can establish
baseline levels of utilization and patient
morbidity, identify key beneficiaries
and subpopulations for proactive care
coordination efforts, and track their
progress against defined performance
measures. These data are especially
important for ACOs made up of small
and individual practices that may not
have fully developed information
technology systems. Additionally,
stakeholders have expressed a desire to
receive updated beneficiary identifiable
claims data on either a monthly or
quarterly basis.
For these reasons we believe sharing
beneficiary identifiable claims data with
ACOs will assist them in improving care
for individuals, improving health of
their population, and reducing the
growth in expenditures for their
assigned beneficiary population.
However, there are clear legal and
practical limitations on how useful
these CMS claims data may be to an
ACO. For example, providers have said
that they would like to know when their
patients are admitted to the hospital in
‘‘real time’’. We are not able to provide
this type of data since we generally only
become aware of a hospital admission at
the time of discharge when the hospital
bills us for the service. So, there will
always be a claims lag that will make
our data less useful for ‘‘real time’’
responses. Unlike claims data, real time
information may be more readily
available through development and use
of an interoperable electronic health
record or participation in local/regional
health information exchanges, or
through more effective coordination
with admitting and discharging
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personnel in hospitals that the ACO’s
patients utilize, something that is
consistent with the overall purpose and
intent of the Shared Savings Program
(see Section II.B. of this proposed rule).
Moreover, unlike MA plans, under the
Shared Savings Program, freedom of
choice for FFS beneficiaries is retained,
which means that a full analysis of the
beneficiary population cared for by the
ACO during the course of the
performance year can only be performed
retrospectively.
It should also be noted that 42 U.S.C.
290dd–2 and implementing regulations
at 42 CFR part 2 restrict the disclosure
of patient records by Federally
conducted or assisted substance abuse
programs, except as expressly
authorized. The law states that ‘‘records
of the identity, diagnosis, prognosis, or
treatment of any patient which are
maintained in connection with the
performance of any program or activity
relating to substance abuse education,
prevention, training, treatment,
rehabilitation, or research, which is
conducted, regulated, or directly or
indirectly assisted by any department or
agency of the United States shall * * *
be confidential.’’ Such data may be
disclosed only with the prior written
consent of the patient, or as otherwise
provided in the statute and regulations.
Consistent with this requirement, claims
containing this specifically protected
information would not be included in
any beneficiary identifiable claims data
shared with ACOs.
As discussed later in the document in
more detail, we are proposing to give
the ACO the opportunity to request
certain beneficiary identifiable claims
data on a monthly basis, in compliance
with applicable laws, in the form of a
standardized data set about the
beneficiaries currently being served by
the ACO participants and ACO
providers/suppliers. We propose to
limit the beneficiaries covered by such
data sets to those who have received a
service from a primary care physician
participating in the ACO during the
performance year, and who have not
opted out of having us share their
claims data with the ACO. In order to
obtain beneficiary information that is
subject to 42 CFR 290dd, the individual
must have provided his or her prior
written consent. Furthermore, we also
propose to limit the content of this data
set to the minimum data necessary for
the ACO to effectively coordinate care of
its patient population.
As noted previously, there are
limitations on the content and
timeliness of data that we can share
with an ACO. If an ACO chooses to
request beneficiary identifiable claims
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data as part of the application process,
we propose that the ACO will be
required to explain how it intends to
use these data to evaluate the
performance of ACO participants and
ACO providers/suppliers, conduct
quality assessment and improvement
activities, and conduct populationbased activities to improve the health of
its assigned beneficiary population. If an
ACO does not choose to request these
data at the time of its application, it will
be required to submit a formal request
for data during the agreement period
that includes a description of how it
intends to use the requested data for the
purposes noted previously. We solicit
comment on these proposals.
Additionally, when an ACO is
accepted to participate in the Shared
Savings Program, we propose to require
ACOs to enter into a Data Use
Agreement (DUA) prior to receipt of any
beneficiary identifiable claims data.
Under the DUA, the ACO would be
prohibited from sharing the Medicare
claims data that we provide through the
Shared Savings Program with anyone
outside the ACO. In addition, we
propose to require in the DUA that the
ACO agree not to use or disclose the
claims data obtained under the DUA in
a manner in which a HIPAA covered
entity could not, without violating the
HIPAA Privacy Rule. We propose to
make compliance with the DUA a
condition of the ACO’s participation in
the Shared Savings Program—noncompliance with this requirement
would result in the ACO no longer being
eligible to receive data, and could lead
to termination from the Shared Savings
Program or additional sanctions and
penalties available under the law. For
example, under the Privacy Act, any
‘‘person who knowingly and willfully
requests or obtains any record
concerning an individual from an
agency under false pretenses shall be
guilty of a misdemeanor and fined not
more than $5,000’’ 5 U.S.C. 552a(i)(3). In
those instances where an ACO does not
choose to request the data at the time of
their application, the ACO will be
required to submit a formal request for
data during the agreement period. We
propose that the ACO would be required
to certify compliance with the DUA in
the same manner in which prospective
ACOs did in the original application
process. We solicit comment on these
proposals.
a. Legal Authority To Disclose
Beneficiary-Identifiable Claims Data to
ACOs
As noted previously, section 1106 of
the Act generally bars the disclosure of
information absent patient authorization
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that is collected under the Act unless a
law (statute or regulation) provides for
disclosure. Once again, we believe that
the HIPAA Privacy Rule permits
disclosure for purposes of sharing
Medicare Part A and B claims data with
ACOs participating in the Shared
Savings Program. Similarly, we believe
the regulations governing the sharing of
Part D data would permit us to share
information regarding prescription drug
claims with ACOs. We also believe that
the proposed disclosures of claims data
under Parts A, B, and D are consistent
with the purposes for which the data
were collected, and thus, for the reasons
discussed previously would be
permitted under the Privacy Act if we
ensure that an appropriate Privacy Act
System of Records ‘‘routine use’’ is in
place prior to making any disclosures.
(1) Sharing Data Related to Medicare
Parts A and B
As discussed in section II.B. of this
proposed rule, the ACOs are tasked with
working with ACO participants and
ACO providers/suppliers to evaluate
their performance, conduct quality
assessment and improvement activities,
and conduct population-based activities
relating to improved health for their
assigned beneficiary population. When
done by or on behalf of a covered entity,
these are covered functions and
activities that would qualify as ‘‘health
care operations’’ under the first and
second paragraphs of the definition of
health care operations at 45 CFR
164.501. These activities are done by the
ACOs either on their own behalf as
covered entities, or on behalf of their
covered entity ACO participants and
ACO providers/suppliers, in which case
the ACOs would be the business
associate of its ACO participants and
ACO providers/suppliers.
The proposed disclosure of Part A and
B claims data would be permitted by the
HIPAA Privacy Rule provisions
governing disclosures for ‘‘health care
operations.’’ As discussed previously in
the context of our proposed disclosure
of the four data elements about the
historically assigned beneficiary
population, a covered entity is
permitted to disclose PHI to another
covered entity for the recipient’s health
care operations if both covered entities
have or had a relationship with the
subject of the records to be disclosed
(which is true here), the records pertain
to that relationship (which is also true
here) and the recipient plans to use the
records for a ‘‘health care operations’’
function that falls within the first two
paragraphs of the definition of ‘‘health
care operations’’ in the HIPAA Privacy
Rule. 45 CFR 164.506(c)(4). The first
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two paragraphs of the definition of
health care operations include a covered
entity or its business associate
evaluating a provider’s or supplier’s
performance, conducting quality
assessment and improvement activities,
and conducting population-based
activities relating to improved health. 45
CFR 164.501. We believe that these
provisions are extensive enough to
cover the uses we would expect an ACO
to make of the Parts A and B claims data
set that we are proposing to make
available to them. Thus, we believe that
there is authority for us to disclose to an
ACO, as the business associate of the
covered entity, the minimum Medicare
Parts A and B data necessary to allow
ACOs to conduct the health care
operation activities outlined previously.
Accordingly, barring a beneficiary
requesting to opt-out of having his or
her information shared as described
later in the document, and subject to
applicable confidentiality laws, we are
proposing to make Part A and Part B
data about patients who have had a visit
with a primary care physicians
participation in the ACO during the
performance year available upon request
to participating ACOs this data would
be used for the purposes of aiding the
ACO as it evaluates the performance of
ACO participants and ACO providers/
suppliers, conducts quality assessment
and improvement activities, and
conducting population-based activities
relating to improved health. In doing so,
we will only disclose the minimum data
necessary to accomplish these purposes
in accordance with the requirements of
the HIPAA Privacy Rule. We believe
that the minimum necessary Parts A and
B data elements would include data
elements such as: Procedure code,
diagnosis code, beneficiary ID; date of
birth; gender; and, if applicable, date of
death; claim ID; the from and thru dates
of service; the provider or supplier ID;
and the claim payment type.
As discussed previously, we will not
disclose any patient information related
to alcohol and substance abuse that is
subject to 42 CFR 290dd without the
patient’s written consent.
Similar to the process by which ACOs
can receive the four beneficiary
identifiable data points, under this
proposal, in order to receive data, ACOs
would be required to attest in either
their initial application or in their
subsequent formal request for data if
they failed to request data in the
application stage, that; (1) They are a
covered entity or a business associate of
covered entity ACO participants and
ACO suppliers/providers under the
Shared Savings Program; (2) their
business associate agreement with these
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ACO participants and ACO providers/
suppliers authorizes them to seek PHI
on behalf of the ACO participants and
ACO providers/suppliers for one of the
health care operations purposes laid out
previously; (3) their request reflects the
minimum data necessary to do that
health care operations work; and (4) that
their use of these requested data would
be limited to the Shared Savings
Program activities related to one or more
of the health care operations purposes
laid out previously or (1) They are a
HIPAA covered entity; (2) they are
requesting the claims data about their
own patients for one of the health care
operations purposes laid out previously;
(3) their request reflects the minimum
data necessary to do that health care
operations work; and (4) that their use
of these requested data would be limited
to the Shared Savings Program activities
related to one or more of the health care
operations purposes laid out previously.
(2) Sharing Data Related to Medicare
Part D
Beneficiary identifiable Medicare
prescription drug information could
also be beneficial to ACOs for improving
the care coordination of their patient
population. Having a complete picture,
for example, of the beneficiary’s
medication regimen can assist in
avoiding duplication or adverse
interactions among medications.
We issued a final rule in May of 2008
authorizing the Secretary to recollect
Part D claims data that were originally
collected for Part D payment purposes
for research, analysis, reporting, and
public health functions (73 FR 30664).
In that final rule, we noted our intent to
use the data for a wide variety of
purposes including ‘‘supporting care
coordination and disease management
programs,’’ and ‘‘supporting quality
improvement and performance
measurement activities.’’ (42 CFR
423.505(f)(3)(v), (vi)). We also expressed
our view that ‘‘it is in the interest of
public health to share the information
collected…with entities outside of CMS
for legitimate research, or in cases of
other governmental agencies, for
purposes consistent with their mission.’’
(73 FR 30666). Accordingly, the
regulations specified when data would
be shared with outside entities, such as
other government agencies, and external
entities, including researchers.
The Part D data rule did not expressly
address the question of whether Part D
data could be shared with external
entities, such as ACOs, for purposes
other than research. However, in the
rule, we noted that sharing Part D
claims data, in addition to Parts A and
B data, could have salutary effects on
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the evaluation and functioning of the
Medicare programs as well as improving
the clinical care furnished to
beneficiaries. Furthermore, the rule
explicitly contemplated the use of Part
D data to support care coordination and
disease management programs, as well
as quality improvement and
performance measurement activities,
which are central to the Shared Savings
Program and its success.
We believe that ACOs participating in
the Shared Savings Program would use
information on prescription drug use in
order to improve the quality of care
furnished to their assigned beneficiaries
and to enhance care coordination for
these beneficiaries. As a result, although
the Part D data rule did not expressly
address the question of whether Part D
data could be shared with external
entities for purposes other than
research, we believe that the release of
Part D claims data to ACOs for the
purpose of supporting care
coordination, quality improvement, and
performance measurement activities,
would be consistent with the purposes
outlined in the Part D data rule. The
Part D data will be released in
accordance with the requirements
outlined in the regulations at 42 CFR
423.505(m)(1). As a result, certain data
elements may be unavailable or
available only in an aggregated format.
Accordingly, consistent with the
regulations governing the release of Part
D data, we propose to provide ACOs
with the minimum Part D data
necessary to permit the ACO to
undertake evaluation of the performance
of ACO participants and ACO
providers/suppliers, conduct quality
assessment and improvement activities
with and on behalf of the ACO
participants and ACO providers/
suppliers, and conduct populationbased activities relating to improved
health for Medicare beneficiaries who
have a primary care visit with a primary
care physician used to assign patients to
the ACO during a performance year. We
propose that the minimum data
elements necessary to perform these
functions could include data elements
such as: beneficiary ID, prescriber ID,
drug service date, drug product service
ID, and indication if the drug is on the
formulary.
a. Beneficiary Opportunity To Opt-Out
of Claims Data Sharing
Although we have the legal authority
within the limits described previously
to share Medicare claims data with
ACOs without the consent of the
patients, and while we believe that
these data will provide a valuable tool
to assist ACOs in evaluating the
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performance of ACO participants and
ACO providers/suppliers, conducting
quality assessment and improvement
activities, and conducting populationbased activities relating to improved
health, we nevertheless believe that
beneficiaries should be notified of, and
have meaningful control over who, has
access to their personal health
information for purposes of the Shared
Savings Program. Thus, we are
proposing to require that, as part of its
broader activities to notify patients at
the point of care that their provider or
supplier is participating in an ACO, as
discussed in Section II. D., the ACO
must also inform beneficiaries of its
ability to request claims data about them
if they do not object. We believe that
this notification will give the
beneficiaries meaningful choice as to
whether this information may be shared.
The only exceptions to this advanced
notice would be the initial four data
points (the beneficiary’s name, date of
birth, sex, and HICN) that we will
provide to ACOs for individuals in the
3-year data set used to determine the
ACO’s benchmark.
We believe that to be meaningful, the
opportunity to make a choice as to
whether their information may be
shared would: (1) Allow the individual
advance notice and time to make a
decision; (2) be accompanied by
adequate information about the benefits
and risks of making their data available
for the proposed uses; (3) not compel
consent; and (4) not use the choice to
permit their information to be shared for
discriminatory purposes.
We considered two alternative
mechanisms for implementing
meaningful beneficiary choice: having
beneficiaries affirmatively choose to
permit us to share their protected health
information through the signing of a
consent or authorization (‘‘opt-in’’); and
sharing protected health information
with the ACO unless beneficiaries
indicate that they choose not to have
this information shared (‘‘opt-out’’).
A requirement of patient choice about
whether to participate in a system of
information exchange, whether opt-in or
opt-out should provide an excellent
opportunity for providers to engage
patients in true patient-centered care,
creating a strong incentive for an ACO
and its ACO participants and ACO
providers/suppliers to forge a positive
relationship with each beneficiary.
Consumers have consistently expressed
strong support for the implementation
and exchange of electronic health
information, believing that these
technologies have the potential to
improve care coordination, reduce
paperwork, and reduce the number of
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19559
unnecessary and repeated tests and
procedures.8 Successful electronic
health information exchange systems
have engaged consumers, physicians
and other stakeholders at an early stage
to ensure that choice is integrated into
the architecture of the systems.9
Many organizations engaging in
health information exchange have
selected opt-in models for patient
consent. For example, the
Massachusetts eHealth Collaborative
(MAeHC) achieved an average of 90
percent participation in three pilot
communities using an opt-in system.
The New York Clinical Information
Exchange (NYCLIX) has also realized
high patient participation rates by using
an opt-in method of patient choice.10 An
opt-in method has several advantages.
Consumers have consistently expressed
a desire that their consent should be
sought before their health information
may be shared.11 Obtaining affirmative
written permission would also provide
documentation of the beneficiary’s
choice.
However, many organizations find
that an opt-in approach significantly
reduces both provider and beneficiary
participation for administrative reasons,
and not because patients are making an
active choice not to participate.12 Where
8 See Schneider, S. et al. ‘‘Consumer Engagement
in Developing Electronic Health Information
System.’’ Prepared for: Agency for Healthcare
Research and Quality, July 2009, at 16. Available
at: https://www.healthit.ahrq.gov/portal/server.pt/
gateway/PTARGS_0_1248_888520_0_0_18/
09%E2%80%900081%E2%80%90EF.pdf%00%00
at 16; Markle Foundation. Survey Finds Americans
Want Electronic Personal Health Information to
Improve Own Health Care, November 2006, at 1.
Available at: https://www.markle.org/
downloadable_assets/research_doc_120706.pdf.
9 See Goldstein, M.M. and A.L. Rein. Consumer
Consent Options for Electronic Health Information
Exchange: Policy Considerations and Analysis,’’
March, 2010. Available at: https://healthit.hhs.gov/
portal/server.pt/gateway/
PTARGS_0_11673_911197_0_0_18/
ChoiceModelFinal032610.pdf.
10 J. Shapiro, J. Bartley, G. Kuperman, Health
Information Exchange Consent Policy Influences:
Emergency Department Patient Data Accessibility.
ACEP 2010. See also N. Daurio, et al.
Implementation of an Enterprise-wide Electronic
Health Record: A Nurse-Physician Partnership, in
K. Saranto et al., eds, Connecting Health and
Humans (IOS Press 2009).
11 Schneider, at 36–37. Public Attitudes Toward
Medical Privacy. (2000). Conducted by The Gallup
Organization on behalf of the Institute for Health
Freedom. Available at: https://forhealthfreedom.org/
Gallupsurvey/IHF–Gallup.html.
12 See Micky Tripathi, David Delano, Barbara
Lund and Lynda Rudolph. ‘‘Engaging Patients for
Health Information Exchange.’’ Health Affairs.
Volume 28, Number 2. March/April 2009; Missouri
Office of Health Information Technology. Opt-in
Versus Opt-out: Consent Models for Health
Information Exchange through Missouri’s Statewide
Health Information Exchange Network. Jefferson
City: Missouri. Department of Social Services
(2010). Available online at https://www.dss.mo.gov/
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opt-in rates are very high, significant
paperwork burdens arise as providers
must track consents for the majority of
their patient population. Reducing such
burdens is one of the major reasons that
other organizations engaged in health
information exchange have adopted an
opt-out approach. 12 13 An opt-out
approach is used successfully in most
systems of electronic exchange of
information 13 because it is significantly
less burdensome on consumers and
providers while still providing an
opportunity for caregivers to engage
with patients to promote trust and
permitting patients to exercise control
over their data. We are concerned about
the effect of an opt-in approach on
beneficiary participation and the
additional administrative burdens on
physician practices. Therefore, we
propose affording beneficiaries the
ability to opt-out of sharing their
protected health information with the
ACO. We believe this opportunity
coupled with notification of how
protected health information will be
shared and used affords beneficiaries
meaningful choice. An example of the
opt-out approach would be that when a
beneficiary has a visit with their
primary care physician, their physician
would inform them at this visit that he
or she is an ACO participant or ACO
provider/supplier and that the ACO
would like to be able to request claims
information from us in order to better
coordinate the beneficiary’s care. If the
beneficiary objects, we propose that the
beneficiary would be given a form
stating that they have been informed of
their physician’s participation in the
ACO and explaining how to opt-out of
having their personal data shared. The
form could include a phone number
and/or e-mail address for beneficiaries
to call and request that their data not be
shared. As discussed in section II. D.,
the Shared Savings Program lays the
foundation for a beneficiary-centered
delivery system that should create a
new relationship between beneficiaries
and care providers based, in large part,
on patient engagement in the new care
hie/leadership/pdf2010/
optin_vs_optout_overview.pdf.
12 See Goldstein, M.M. and A.L. Rein. Consumer
Consent Options for Electronic Health Information
Exchange: Policy Considerations and Analysis,’’
March, 2010, at 35. Available at: https://
healthit.hhs.gov/portal/server.pt/gateway/
PTARGS_0_11673_911197_0_0_18/
ChoiceModelFinal032610.pdf.
13 See Goldstein, M.M. and A.L. Rein. Consumer
Consent Options for Electronic Health Information
Exchange: Policy Considerations and Analysis,’’
March, 2010, at 35. Available at: https://
healthit.hhs.gov/portal/server.pt/gateway/
PTARGS_0_11673_911197_0_0_18/
ChoiceModelFinal032610.pdf.
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system. The successful creation of this
relationship is not possible when
beneficiaries are not aware of the new
delivery system available through
ACOs, and the possibility of being
included in the population assigned to
an ACO.
We therefore propose to develop a
communications plan, discussed in
more detail in section II. D of this
proposed rule, that will offer insight
into both the Shared Savings Program in
general and the beneficiaries’ right to
opt-out of the data sharing portion of the
ACO Shared Savings Program.
As noted previously, ACOs will only
be allowed to request beneficiary
identifiable claims data for beneficiaries
who have (1) visited a primary care
participating provider during the
performance year, and (2) have not
chosen to opt-out of claims data sharing.
A beneficiary that chooses to opt-out
is only opting out of the data sharing
portion of the program. The decision to
opt-out in no way effects use of the
beneficiaries’ data or assignment to the
ACO for purposes of determining such
calculations as ACO benchmarks, per
capita costs, quality performance, or
performance year per capita
expenditures. Our data contractor will
maintain a running list of all HICNs that
have chosen to opt-out of data sharing.
We will monitor whether ACOs
continue to request data on beneficiaries
who have opted out of having their data
shared and will take appropriate actions
against any ACO that is found to violate
this requirement.
We request comments on our
proposals related to the provision of
both aggregate and beneficiary
identifiable data to ACOs. We are
particularly interested in comments on
the kinds and frequency of data that
would be useful to ACOs, potential
privacy and security issues, and the
implications for sharing protected
health information with ACOs, and the
use of a beneficiary opt-out, as opposed
to an opt-in, to obtain beneficiary
consent to the sharing of their
information.
7. New Program Standards Established
During 3-Year Agreement Period
The Shared Savings Program is a new
program designed to encourage
providers to redesign care processes in
order to achieve the outcomes of better
care for individuals, better health for
populations, and lower growth in
expenditures for Medicare FFS
beneficiaries. We anticipate that as we
continue to work with the stakeholder
community and learn what methods and
measures work most effectively for the
Shared Savings Program, we will make
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changes and improvements to the
Shared Savings Program. For example,
we expect to integrate lessons learned
from Innovation Center initiatives to
shape and change the Shared Savings
Program over time. Because we expect
that these changes may occur more
frequently than the length of the 3-year
agreement periods, the question arises
as to whether those ACOs that have
already committed to a 3-year agreement
to participate in the Shared Savings
Program should be subject to those
changes. It is not unprecedented for
Medicare agreements to include a
provision requiring that the agreement
is subject to changes in laws and
regulations. For example, the contracts
with Medicare Advantage organizations
contain such a clause. However, these
contracts are for a term of 1 year, as
opposed to 3 or more years. As a result,
there are more frequent opportunities
for these organizations to reassess
whether they wish to continue to
participate in the program in light of
changes to the laws and regulations
governing the program.
In the Shared Savings Program,
regulatory changes could affect a variety
of different components of the program,
including quality measures, reporting
requirements, monitoring requirements,
program integrity, and eligibility
requirements. If the agreements are
subject to all changes in the applicable
regulations, it is possible that some
ACOs that were eligible for participation
in the program at the start of their
respective 3-year agreement might
become ineligible based upon
modifications to the regulations.
Creating an environment in which the
continued eligibility of existing program
participants is uncertain could be
detrimental to the success of program
and could deter program participation.
Conversely, the ability to incorporate
regulatory changes into the agreements
with ACOs would facilitate the
administration of the program because
all ACOs would be subject to the
requirements imposed under the current
regulations, rather than up to 3 different
sets of requirements, based upon the
year in which the ACO entered the
program. Additionally, requiring ACOs
to adhere to certain regulatory changes
related to quality measures, routine
program integrity changes, processes for
quality management and patient
engagement, and patient-centeredness
criteria that are up to date with current
clinical practice ensures that ACO
activities keep pace with changes in
clinical practices and developments in
evidence-based medicine. We do not
believe that requiring ACOs to adhere to
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regulatory modifications related to
quality measures, routine program
integrity changes, processes for quality
management and patient engagement,
and patient centeredness criteria is
likely to affect either the ACOs’
underlying organizational structure or
their continued eligibility to participate
in the Shared Savings Program—
although it may necessitate changes in
how ACOs design and deliver care to
meet these program requirements, as
compared to descriptions of these
processes in their initial applications.
We propose that ACOs be subject to
future changes in regulation with the
exception of the following program
areas:
• Eligibility requirements concerning
the structure and governance of ACOs;
• Calculation of sharing rate; and
• Beneficiary assignment.
For example, ACOs would be subject
to changes in regulation related to the
quality performance standard. The
language of the ACO agreement would
be explicit to ensure that ACOs
understand the dynamic nature of this
part of the program and what specific
programmatic changes would be
incorporated into the agreement. We
further propose that in those instances
where regulatory modifications
effectuate changes in the processes
associated with an ACO pertaining to
design, delivery, and quality of care that
the ACO will be required to submit to
us for review and approval, as a
supplement to their original application,
an explanation of how they will address
key changes in processes resulting from
these modifications. If an ACO fails to
effectuate the changes needed to adhere
to the regulatory modifications, we
propose that the ACO would be placed
on a corrective action plan, and if after
being given an opportunity to act upon
the corrective action plan, the ACO still
fails to come into compliance, it would
be terminated from the program. For a
more detailed discussion of the process
for requiring and implementing a
corrective action plan, please refer to
the section II. H. of this proposed rule.
We propose that ACO participants shall
continue to be subject to all
requirements applicable to FFS
Medicare, such as routine CMS business
operations updates and changes in FFS
coverage decisions, as they may be
amended from time to time. In other
words, nothing in the Shared Savings
Program shall be construed to affect the
payment, coverage, program integrity,
and other requirements that apply to
providers and suppliers under FFS
Medicare.
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8. Managing Significant Changes to the
ACO During the Agreement Period
Aside from changes that an ACO may
experience as a result of regulatory
changes, the ACO itself may also
experience significant changes within
the course of its 3-year agreement period
due to such events as: The following:
• Deviations from approved
application for reasons such as the drop
out of an ACO participant upon which
assignment is based; changes in overall
governing board composition (in terms
of interests represented) or leadership;
changes in ACO’s eligibility to
participate in the program, including
changes to the key processes pertaining
to the design, delivery and quality of
care (such as processes for quality
management and patient engagement
and patient centeredness criteria) as
outlined in the application criteria for
acceptance into the program; or changes
in planned distribution of shared
savings.
• A material change, as defined in
detail in section II. H. of ACOs of this
proposed rule, in the ACOs provider
composition, including the addition of
ACO providers/suppliers such that the
ACO requires a mandatory antitrust
review or re-review as discussed in
section II. I. Coordination with Other
Agencies., and other circumstances
under which an ACO or an ACO
participant is unable to complete its
3-year commitment.
• Government-required ACO
reorganization, or exclusion of ACO
participants or ACO providers/
suppliers, or conduct restriction due to:
OIG excluding the ACO, an ACO
participant, or an ACO provider/
supplier for any reason authorized by
law; CMS revoking an ACO, ACO
participant or ACO provider/supplier’s
Medicare billing privileges under
42 CFR 424.535, for noncompliance
with billing requirements or other
prohibited conduct; or reorganization or
conduct restrictions to resolve antitrust
concerns.
Whenever an ACO reorganizes its
structure, we must determine if the ACO
remains eligible to participate in the
Shared Savings Program. Since an ACO
is admitted to the program based on its
application, adding ACO participants
during the course of the 3-year
agreement may deviate from its
approved application and jeopardize the
ACO’s eligibility since the ACO would
differ from its approved application and
could be subject to further antitrust
review. Changes such as this may result
in termination of the 3-year agreement
and forfeiture of the 25 percent
withhold of shared savings earned by
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the original ACO participants. We
therefore propose that the ACO may not
add ACO participants during the course
of the 3-year agreement. In order to
maintain flexibility, however, we
propose that the ACO may remove ACO
participants (TINs) or add/subtract ACO
providers/suppliers (NPIs). We request
comment on this proposal that ACOs
may not add ACO participants and how
this proposal might impact small or
rural ACOs. We propose that the ACO
be required to notify us in order to have
its new structure approved whenever
significant changes, such as those
referenced previously, occur to its
structure. We have identified five
outcomes that may result from our
review:
• The ACO may continue to operate
under the new structure with savings
calculations for the performance year
based upon the updated list of ACO
participants and ACO providers/
suppliers.
• The remaining ACO structure
qualifies as an ACO but is so different
from the initially approved ACO
structure that the ACO must start over
as a new ACO with a new 3-year
agreement, including an antitrust
review, if warranted.
• The remaining ACO structure
qualifies as an ACO but is materially
different from the initially approved
ACO structure because of the inclusion
of additional ACO providers/suppliers
that the ACO must obtain approval from
a reviewing Antitrust Agency before it
can continue in the program.
• The remaining ACO structure no
longer meets the eligibility criteria for
the program, and the ACO would no
longer be able to participate in the
program, for example, if the ACO’s
assigned population falls below 5,000
during an agreement year as discussed
in section II. B. of this proposed rule.
• CMS and the ACO may mutually
decide to terminate the agreement.
We propose that when an ACO
reorganizes its structure by excluding
ACO participants or by adding or
excluding ACO providers/suppliers,
deviates from its approved application,
changes information contained in its
approved application, or experiences
other changes which may make it
unable to complete its 3-year agreement,
it must notify us within 30 days of the
event for reevaluation of its eligibility to
continue to participate in the Shared
Savings Program. We would respond in
one of the five ways specified
previously. We request comment on this
proposal.
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9. Future Participation of Previously
Terminated Program Participants
disincentives for participation among
smaller entities.
As described in section II.H. of the
proposed rule, there are a number of
circumstances under which we may
terminate our agreement with an ACO,
including avoidance of at-risk
beneficiaries and failure to meet the
quality performance standards. In
contrast, there are also many reasons
why an ACO participant TIN, used for
assignment, or individual ACO
providers/suppliers may drop out of an
ACO; such as government exclusion,
relocation, retirement, a voluntary
decision to terminate participation, or
bankruptcy.
Permanently barring former program
participants from subsequent
participation in the Shared Savings
Program due to a voluntary or forced
termination from an ACO appears
unduly harsh given the dynamic nature
of organizational membership.
Alternatively, we do want to ensure our
policy on subsequent participation in
the Shared Savings Program does not
provide a second chance for underperforming organizations or to providers
or suppliers who have been terminated
for failing to meet program integrity
requirements.
We propose the ACO disclose to CMS
whether the ACO, its ACO participants,
or its ACO providers/suppliers have
participated in the program under the
same or a different name, and specify
whether it was terminated or withdrew
voluntarily from the program. If the
ACO, its ACO participants or ACO
providers/suppliers were previously
terminated from the program, the
applicant must identify the cause of
termination and what safeguards are
now in place to enable the prospective
ACO to participate in the program for
the full period of the 3-year agreement
period. We propose that such ACOs may
not begin another 3-year agreement
period until the original agreement
period has lapsed. Additionally,
because we believe that subsequent
participation in the Shared Savings
Program should not provide a second
chance for under-performing
organizations, we propose that an ACO
may not reapply to participate in the
Shared Savings Program if it previously
experienced a net loss during its first
3-year agreement period. We seek
comment on these proposals and
whether requirements for denying
participation to ACOs that previously
under-perform would create
disincentives for the formation of ACOs.
We are specifically interested in
whether this requirement will create
D. Assignment of Medicare Fee-forService Beneficiaries
Section 1899(c) of the Act, as added
by section 3022 of the Affordable Care
Act, requires the Secretary to ‘‘determine
an appropriate method to assign
Medicare FFS beneficiaries to an ACO
based on their utilization of primary
care services provided under this title
by an ACO professional described in
subsection (h)(1)(A).’’ Subsection
1899(h)(1)(A) of the Affordable Care Act
constitutes one element of the definition
of the term ‘‘ACO professional.’’
Specifically, this subsection establishes
that ‘‘a physician (as defined in section
1861(r)(1))’’ is an ‘‘ACO professional’’ for
purposes of the Shared Savings
Program. Section 1861(r)(1) of the Act in
turn defines the term physician as
‘‘* * * a doctor of medicine or
osteopathy legally authorized to practice
medicine and surgery by the State in
which he performs such function or
action.’’ In addition, subsection
1899(h)(1)(B) defines an ACO
professional to include practitioners
described in section 1842(b)(18)(C)(i) of
the Act, such as PAs and NPs.
Thus, although the statute defines the
term ‘‘ACO professional’’ to include both
physicians and non-physician
practitioners, such as advance practice
nurses, physician assistants, and nurse
practitioners, for purposes of beneficiary
assignment to an ACO, the statute
requires that we consider only
beneficiaries’ utilization of primary care
services provided by ACO professionals
who are physicians. The method of
assigning beneficiaries therefore must
take into account the beneficiaries’
utilization of primary care services
rendered by physicians. Therefore, for
purposes of the Shared Savings
Program, the inclusion of practitioners
described in section 1842(b)(18)(C)(i) of
the Act, such as PAs and NPs in the
statutory definition of the term ‘‘ACO
professional’’ is a factor in determining
the entities that are eligible for
participation in the program (for
example, ‘‘ACO professionals in group
practice arrangements’’ in section
1899(b)(1)(A) of the Act). However,
assignment of beneficiaries to ACOs is
to be determined only on the basis of
primary care services provided by ACO
professionals who are physicians.
Assigning Medicare beneficiaries to
ACOs also requires several other
elements: (1) An operational definition
of an ACO (as distinguished from the
formal definition of an ACO and the
eligibility requirements that we discuss
in section II.B. of this proposed rule) so
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that ACOs can be efficiently identified,
distinguished, and associated with the
beneficiaries for whom they are
providing services; (2) a definition of
primary care services for purposes of
determining the appropriate assignment
of beneficiaries; (3) a determination
concerning whether to assign
beneficiaries to ACOs prospectively, at
the beginning of a performance year on
the basis of services rendered prior to
the performance year, or retrospectively,
on the basis of services actually
rendered by the ACO during the
performance year; and (4) a
determination concerning the
proportion of primary care services that
is necessary for a beneficiary to receive
from an ACO in order to be assigned to
that ACO for purposes of this program.
The term ‘‘assignment’’ in this context
refers only to an operational process by
which Medicare will determine whether
a beneficiary has chosen to receive a
sufficient level of the requisite primary
care services from physicians associated
with a specific ACO so that the ACO
may be appropriately designated as
exercising basic responsibility for that
beneficiary’s care. Consistent with
section 1899(b)(2)(A), the ACO will then
be held accountable ‘‘for the quality,
cost, and overall care of the Medicare
FFS beneficiaries assigned to it.’’ The
ACO may also qualify to receive a share
of any savings that are realized in the
care of these assigned beneficiaries due
to appropriate efficiencies and quality
improvements that the ACO may be able
to implement. It is important to note
that the term ‘‘assignment’’ for purposes
of this provision in no way implies any
limits, restrictions, or diminishment of
the rights of Medicare FFS beneficiaries
to exercise complete freedom of choice
in the physicians and other health care
practitioners and suppliers from whom
they receive their services.
Thus, while the statute refers to the
assignment of beneficiaries to an ACO,
we would characterize the process more
as an ‘‘alignment’’ of beneficiaries with
an ACO as the exercise of free choice by
beneficiaries in the physicians and other
health care providers and suppliers
from whom they receive their services is
a presupposition of the Shared Savings
Program. Therefore, an important
component of the Shared Savings
Program will be timely and effective
communication with beneficiaries
concerning the Shared Savings Program,
their possible assignment to an ACO,
and their retention of freedom of choice
under the Medicare FFS program. The
issues of beneficiary information and
notification regarding their potential
assignment to an ACO are further
discussed at the end of this section.
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1. Operational Identification of an ACO
The first step in developing a method
for assigning beneficiaries is to establish
a clear operational method of
identifying an ACO that correctly
associates its health care professionals
and providers with the ACO. It is
designed to be consistent with the
statutory definition of an ACO as well
as the eligibility and other requirements
for an organization to participate in the
Shared Savings Program as an ACO. As
discussed in section II.B. of this
proposed rule, section 1899(a)(1)(A) of
the Act defines ACOs as ‘‘groups of
providers of services and suppliers’’
who work together to manage and
coordinate care for Medicare fee-forservice beneficiaries. More specifically,
the Act refers to group practice
arrangements, networks of individual
practices of ACO professionals,
partnerships or joint venture
arrangements between hospitals and
ACO professionals, hospitals employing
ACO professionals, or other
combinations that the Secretary
determines appropriate.
From a technical, operational
perspective, there are two data sources
that could be used to identify the
specific providers of services and
suppliers participating in these kinds of
arrangements as ACOs—specifically,
their—(1) National Provider Identifier
(NPI); and (2) TIN. Under the Medicare
program, individual practitioners are
defined by their NPI, but generally file
and receive payment for Medicare
claims based on their TIN. The TIN may
be an employer identification number
(EIN) or social security number (SSN).
Some individual physicians and other
ACO professionals, for example, do not
have EINs, and enroll in the Medicare
program through their SSNs. Physicians
and other ACO professionals who are
members of a group practice and bill for
their services through the group may not
have individual EINs but may use a
group EIN for billing Medicare rather
than their individual SSNs. While all
physicians and practitioners have TINs
(either EINs or SSNs), not all physicians
and practitioners have Medicare
enrolled TINs. For example, physicians
and other ACO professionals who are
members of a group practice often bill
for their services through the group and
may not have individual Medicare
enrolled TINs. Groups of physicians and
practitioners, however, necessarily have
TINs which they employ for billing
Medicare, because a TIN must be used
for billing purposes. It should be noted
that, under the Shared Savings Program,
the standard restrictions on disclosure
of information apply. (For a discussion
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regarding the public disclosure of
information under the Shared Savings
Program, see the discussion in section
II.E. of this proposed rule.)
Under the PGP demonstration,
beneficiaries were assigned and group
quality performance was measured by
identifying practices operationally as a
collection of Medicare enrolled TINs.
Through this demonstration we found
that TINs provide the most direct link
between the beneficiary and the practice
providing primary care services.
Further, TINs are more stable than NPIs
and more likely to provide complete
longitudinal data required for
benchmarking and beneficiary
assignment, and to promote the stability
necessary for the ACO to commit to
redesigning care processes and complete
the required 3-year agreement period.
The reason NPIs tend to be less stable
is because individual physicians and
practitioners often change from one
practice to another, potentially
rendering data continuity and
beneficiary assignment problematic
when only NPIs are available. In the
PGP demonstration, the individual NPIs
associated with the TIN were identified
from claims data and provider
enrollment information, providing for
more effective monitoring of
performance within the ACO. Finally,
reporting at the TIN level appeared to
reduce the reporting burden for
practices participating in the PGP
demonstration.
Therefore, we are proposing to
identify an ACO operationally as a
collection of Medicare enrolled TINs.
More specifically, an ACO will be
identified operationally as a set of one
or more TINs currently practicing as a
‘‘group practice arrangement’’ or in a
‘‘network’’ such as where ‘‘hospitals are
employing ACO professionals’’ or where
there are ‘‘partnerships or joint ventures
of hospitals and ACO professionals’’ as
stated under section 1899(b)(1)(A)
through (E) of the Act. For example, a
single group practice that participates in
the Shared Savings Program would be
identified by its TIN. A network of
independent practices that forms an
ACO would be identified by the set of
TINs of the practices constituting the
ACO. We are proposing to require that
organizations applying to be an ACO
provide their ACO participant TINs.
Each TIN can be systematically linked
to an individual physician specialty
code by us. Therefore, under this
approach, beneficiaries would be
assigned to an ACO through a TIN based
on the primary care services they
received from physicians billing under
that TIN.
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We also propose that ACO
professionals within the respective TIN
on which beneficiary assignment is
based, will be exclusive to one ACO
agreement in the Shared Savings
Program. This exclusivity will only
apply to the primary care physicians
(defined as physicians with a
designation of internal medicine,
geriatric medicine, family practice, and
general practice, as discussed in this
rule) by whom beneficiary assignment is
established.
ACO participant TINs upon which
beneficiary assignment is not dependent
(for example, acute care hospitals,
surgical and medical specialties, RHCs,
and FQHCs) would be required to agree
to participate in the ACO for the term
of the 3-year agreement, but would not
be restricted to participation in a single
ACO. As stated in section II.G. of this
proposed rule, competition in the
marketplace promotes quality of care for
Medicare beneficiaries, protects access
to a variety of providers, and helps
sustain the Medicare program by
controlling cost pressures. All of these
benefits to Medicare patients would be
reduced or eliminated if we allow the
creation of ACOs with significant
market power. This is especially
important in certain areas of the country
that might not have many specialists. In
addition, exclusivity of ACO participant
TINs upon which beneficiary
assignment is not dependent might also
contribute to the prospects that ACOs
could develop excessive market power,
especially in areas with shortages of
physicians. In turn, greater market
power could provide opportunities for
these organizations to engage in
activities that raise issues of fraud and
abuse, such as those related to selfreferrals. For these reasons, physicians
upon whom assignment is dependent
would be committed for a 3-year period
and be exclusive to one ACO.
Conversely, to ensure that physicians
and other entities upon which
assignment is not dependent (that is,
hospitals, FQHC, RHCs, specialists) can
participate in more than one ACO, and
thereby facilitate the creation of
competing ACOs, these providers and
suppliers would be committed to the
3-year agreement but would not be
exclusive and would have the flexibility
to join another ACO.
Based on our experience, we
recognize that the TIN level data alone
will not be entirely sufficient for a
number of purposes in the Shared
Savings Program. In particular, NPI data
will be useful to assess the quality of
care furnished by an ACO. For example,
NPI information will be necessary to
determine what percent of physicians
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and other practitioners in the ACO are
registered in the HITECH program
(discussed in section II.E. of this
proposed rule). NPI data will also be
helpful in our monitoring of ACO
activities (which we discuss in section
II.H. of this proposed rule). Therefore,
we are also proposing to require that
organizations applying to be an ACO
must provide not only their TINs but
also a list of associated NPIs for all ACO
professionals, including a list that
separately identifies physicians that
provide primary care. As we discuss in
more detail later in the document, for
purposes of the Shared Savings
Program, we are proposing to define
primary care physicians as those
physicians that practice in the areas of
internal medicine, general practice,
family practice, and geriatric medicine.
We welcome comments on our proposal
to require reporting of TINs along with
information about the NPIs associated
with the ACO.
In summary, we believe that our
proposal to define the ACO
operationally as a group of Medicareenrolled TINs, while also collecting
information about the NPIs associated
with those TINs, allows us to link the
beneficiary, type of service provided,
and the type of physician providing the
services for purposes of beneficiary
assignment to the ACO as required by
statute. This approach also offers the
most complete longitudinal data
required for benchmarking and
beneficiary assignment, most effectively
limits administrative burden for
participating providers and suppliers,
and makes it possible for us to take
advantage of infrastructure and
methodologies already developed for
group-level reporting and evaluation.
Moreover, this option affords us the
most flexibility and statistical stability
for monitoring and evaluating quality
and outcomes for the population of
patients assigned to the ACO.
2. Definition of Primary Care Services
Section 1899(c) of the Act requires the
Secretary to assign beneficiaries to an
ACO ‘‘based on their utilization of
primary care services’’ provided by a
physician. However, the statute does not
specify which kinds of services should
be considered ‘‘primary care services’’
for this purpose, nor the amount of
those services that would be an
appropriate basis for making
assignments. We discuss issues
concerning the appropriate proportion
of such services in the next section. In
this section of this proposed rule, we
discuss how to identify the appropriate
primary care services on which to base
the assignment and our proposal for
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defining primary care services for this
purpose.
In order to ensure the statistical
reliability of the required performance
measurements and benchmarks, ACOs
must have a sufficient number of
assigned beneficiaries. Having too few
beneficiaries assigned to a participating
ACO will impede determining whether
changes in cost and quality measures
are likely a reflection of normal
variation rather than real improvement
in the delivery of care. Section
1899(b)(2)(D) of the Act specifically
provides that the composition of the
ACO shall include sufficient numbers of
ACO primary care professionals so that
at least 5,000 beneficiaries are assigned
to the ACO.
Primary care services can generally be
defined based on the type of service
provided or the type of provider
specialty that provides the service. The
PGP demonstration has helped inform
assignment methodologies. Under the
PGP demonstration, the assignment
methodology incorporated outpatient
evaluation and management (E&M)
services provided by both primary care
and specialist providers. One reason for
this is that certain specialists (for
example, cardiologists,
endocrinologists, neurologists,
oncologists) are often the principal
primary care provider for elderly and
chronically ill patients who do not
otherwise have a primary care provider,
and it is reasonable to expect them to
take responsibility for these patients’
care. Another reason is that the
assignment methodology provided an
opportunity for specialists to take
responsibility for ensuring that their
patients’ primary care needs were being
met even if the specialist provided care
initially on a referral basis.
We would note that in defining
primary care services, certain Affordable
Care Act provisions also rely on a blend
of the type of service and type of
provider delivering the service. For
example, section 5501 of the Affordable
Care Act makes incentive payments
available to primary care practitioners
for whom primary care services account
for at least 60 percent of the allowed
charges under Part B. For purposes of
this provision, a ‘‘primary care
practitioner’’ is defined as a physician
‘‘who has a primary specialty
designation of family medicine, internal
medicine, geriatric medicine, or
pediatric medicine,’’ or as a ‘‘nurse
practitioner, clinical nurse specialist, or
physician assistant.’’ In that section,
‘‘primary care services’’ are defined as a
set of services identified by these
HCPCS codes: 99201 through 99215;
99304 through 99340; and 99341
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through 99350. Additionally, we would
consider the Welcome to Medicare visit
(G0402) and the annual wellness visits
(G0438 and G0439) as primary care
services for purposes of the Shared
Savings Program.
In developing our proposal, we have
considered three options with respect to
defining ‘‘primary care services’’ for the
purposes of assigning beneficiaries
under the Shared Savings Program: (1)
Assignment of beneficiaries based upon
a predefined set of ‘‘primary care
services;’’ (2) assignment of beneficiaries
based upon both a predefined set of
‘‘primary care services’’ and a predefined
group of ‘‘primary care providers;’’ and
(3) assignment of beneficiaries in a stepwise fashion. Under this option,
beneficiary assignment would proceed
by first identifying primary care
physicians (internal medicine, family
practice, general practice, geriatric
medicine) who are providing primary
care services, and then identifying
specialists who are providing these
same services for patients who are not
seeing any primary care professional.
The first option would assign
beneficiaries by defining ‘‘primary care
services’’ on the basis of the select set of
E&M services, specifically those defined
as ‘‘primary care services’’ in section
5501 of the Affordable Care Act, and
including G-codes associated with the
annual wellness visit and Welcome to
Medicare benefit regardless of provider
specialty. This option would increase
the number of potential beneficiaries
assigned to the ACO in areas with
primary care shortages (where
specialists would necessarily be
providing more primary care services as
defined by the code set). It is also
administratively straightforward, and
we have experience with the similar
methodology initially used in the PGP
demonstration. However, assigning
beneficiaries to ACOs based only on
primary care services without
distinction of caregiver specialty
increases the likelihood of assigning
beneficiaries to a specialist over a
primary care provider. In addition, it
would appear to be somewhat
inconsistent with section 5501 of the
Affordable Care Act, which, for
purposes of establishing an incentive
payment for primary care services, first
defines a set of primary care
practitioners, and then identifies a set of
HCPCS codes as ‘‘primary care services.’’
The primary care services are
recognized for the incentive payment
only when they are provided by primary
care practitioners. It is dubious whether
the codes identified in section 5501 of
the Affordable Care Act alone, when
they are not provided by primary care
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doctors and other practitioners, truly
constitute primary care services. Rather,
these codes alone simply represent
outpatient cognitive services (generally,
consultations and office visits) that are
provided for in all sorts of health care
situations, including primary care but
also specialty care, and are provided by
many types of physicians. As such, this
option has the potential to diminish the
appropriate level of emphasis on a
primary care core in the Shared Savings
Program, by failing to place any priority
on the services of designated primary
care providers (for example, internal
medicine, general practice, family
practice, and geriatric medicine) in the
assignment process.
The second option that we have
considered is therefore to assign
beneficiaries to physicians designated as
primary care providers (internal
medicine, general practice, family
practice, and geriatric medicine) who
are providing the appropriate primary
care services to beneficiaries. As in the
case of the first option, we would define
‘‘primary care services’’ on the basis of
the select set of HCPCS codes identified
in section 5501 of the Affordable Care
Act, including G-codes associated with
the annual wellness visit and Welcome
to Medicare visit. This option more
closely aligns the definition of primary
care services with the definition in
section 5501 of the Affordable Care Act.
As in the case of the first option, this
option would be relatively
straightforward administratively.
However, this option could reduce the
number of beneficiaries assigned to an
ACO, by excluding primary care
services delivered by specialists,
especially in some areas that may have
shortages of primary care physicians but
a relatively greater number of
specialists. Consequently, this option
could make it difficult for ACOs to form
in some geographic regions with such
primary care shortages.
The third option we have considered
is to assign beneficiaries in a step-wise
fashion. Under this option, beneficiary
assignment would proceed by first
identifying primary care physicians
(internal medicine, family practice,
general practice, geriatric medicine)
who are providing primary care
services, and then identifying specialists
who are providing these same services
for patients who are not seeing any
primary care professional. This option
would introduce a greater level of
operational complexity compared to the
two other options we considered. In
addition, it could undermine our goal of
ensuring competition among ACOs by
reducing the number of specialists that
can participate in more than one ACO,
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since specialists to whom beneficiaries
are assigned would be required to be
exclusive to one ACO. As noted
previously, the ability of specialists to
participate in more than one ACO is
especially important in certain areas of
the country that might not have many
specialists. On the other hand, a ‘‘stepwise approach’’ would not affect all
specialists and it would reflect many of
the advantages of the other two
approaches, balancing the need for
emphasis on a primary care core with a
need for increased assignment numbers
in areas with primary care shortages.
After considering these options, we
are proposing the second option, which
would assign beneficiaries with
physicians designated as primary care
providers (internal medicine, general
practice, family practice, and geriatric
medicine) who are providing the
appropriate primary care services to
beneficiaries. We believe that this
option best aligns with other Affordable
Care Act provisions related to primary
care by placing an appropriate level of
emphasis on a primary care core in the
Shared Savings Program. That is, this
option places priority on the services of
designated primary care physicians (for
example, internal medicine, general
practice, family practice, and geriatric
medicine) in the assignment process.
This option also allows ACOs to focus
their efforts to coordinate and redesign
care for patients seeing primary care
providers and creates incentives for
ACOs to establish primary care linkages
for their patients who may not have a
primary care provider. The option is
also relatively straightforward
administratively.
However, we are also concerned that
this proposal may not adequately
account for primary care services
delivered by specialists, especially in
certain areas with shortages of primary
care physicians, and that it may make it
difficult to obtain the minimum number
of beneficiaries to form an ACO in
geographic regions with such primary
care shortages. Therefore, while we are
proposing to assign beneficiaries to
physicians designated as primary care
providers (internal medicine, general
practice, family practice, and geriatric
medicine) who are providing the
appropriate primary care services to
beneficiaries, we invite comments on
this proposal and other options that may
better address the delivery of primary
care services by specialists. In the final
rule, we could consider adopting
another option; therefore we are seeking
comments on the definition of primary
care services approach as well as the
‘‘step-wise’’ approach as described
previously.
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3. Prospective vs. Retrospective
Beneficiary Assignment To Calculate
Eligibility for Shared Savings
Section 1899(d)(1) of the Act provides
that an ACO may be eligible for shared
savings with the Medicare program if
the ACO meets performance standards
established by the Secretary (which we
discuss in section II.E. of this proposed
rule) and meets the requirements for
realizing savings for its assigned
beneficiaries against the benchmark
established by the Secretary under
section 1899(d)(1)(B) of the Act. Thus,
for each year of an agreement period
each ACO will have an assigned
population of beneficiaries. Eligibility
for shared savings will be based on
whether the requirements for receiving
shared savings payments are met for this
assigned population. We refer to each
year for which such determinations
must be made as a ‘‘performance year.’’
There are two basic options for
assigning beneficiaries to an ACO to
calculate eligibility for shared savings
for a performance year. The first option
is that beneficiary assignment could
occur at the beginning of the
performance year, or prospectively,
based on utilization data demonstrating
the provision of primary care services to
beneficiaries in prior periods. The
second option is that beneficiary
assignment could occur at the end of the
performance year, or retrospectively,
based on utilization data demonstrating
the provision of primary care services to
beneficiaries by ACO physicians during
the performance year.
Many observers and prospective ACO
managers have argued that it is essential
for an ACO to know who is included in
its assigned population prior to the start
of the performance year. While they
intend to treat all patients the same,
they assert that it is fundamental to
population management to be able to
profile a population, identify
individuals at high risk, develop
outreach programs, and proactively
work with patients and their families to
establish care plans. These observers
also argue that, as with any well
managed enterprise, it is essential to
have operational goals and targets to
manage effectively. Thus, they would
like to be able to track prospective
targeted expenses, in order to gauge
their results as they go through the
performance year. These observers also
understand that even prospective
assignment methodologies will require a
retrospective definition of the
population to adjust for a variety of
changes in the population that occur
during a performance year. Some
current patients of the practice will
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become eligible for Medicare. Some will
join a Medicare Advantage (MA) plan
and, although they may continue to
receive care furnished by the ACO,
these beneficiaries can no longer be
considered part of the assigned
population of the ACO for purposes of
computing shared savings. Individuals
will move in and out of the service area
during the year. For all these reasons,
any methodology will require a
retrospective redefinition of the
assigned population.
Advocates for the retrospective
approach start with the observation that
the actual population seen by a set of
physicians changes significantly from
year to year. Medicare FFS beneficiaries’
right to see any enrolled physician
typically leads to more year-to-year
variability in treating physicians
compared to patients in managed care
programs. Analysis of the PGP
population did show approximately a
25 percent variation in assignment from
year to year. Prospective assignment of
a population seems inherently
inaccurate from this perspective. If
beneficiary assignment changes by 25
percent from year to year, a prospective
assignment would not be an accurate
reflection of those beneficiaries that
were actually seen by physicians in the
ACO during the performance year.
Retrospective assignment of the
population, on the other hand,
appropriately holds the ACO
accountable for the actual population it
cared for during the performance year.
Proponents of the retrospective
approach also make a second argument.
They suggest that identifying a
population prospectively may lead an
ACO to focus only on providing care
coordination and other ACO services to
this limited population, ignoring other
beneficiaries in their practices or
hospitals. Given that the goal of the
Shared Savings Program is to change the
care experience for all beneficiaries,
ACOs should not be told who among
their patients are likely to be in their
assigned population. ACO participants
and ACO providers/suppliers should
have incentives to treat all patients
equally, using standardized evidencebased care processes, to improve the
quality and efficiency of all of the care
they provide, and in the end they
should see positive results in the
retrospectively assigned population.
We believe there are merits in both
approaches. It does seem appropriate for
an ACO to have information regarding
the population it will likely be
responsible for in order to target its care
improvements to those patients who
would benefit the most. At the same
time, we do not want to encourage
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ACOs to limit their care improvement
activities to a subset of their patients
that they believe may be assigned to
them. Finally, we believe it is critical
that the assessment of ACO performance
in any year be based on patients who
received the plurality of their primary
care from the ACO in that year, rather
than an earlier period. As noted
previously, even under a prospective
assignment approach, a retrospective
redefinition of the assigned population
to account for changes from prior
periods would be required or the ACO
would be held accountable for patients
that it did not provide services for
during the performance year. Under a
prospective system, the assignment
would have to be adjusted every year to
account for beneficiaries entering and
leaving FFS Medicare as well as for
those patients who move in and out of
the geographic area of the ACO, as well
as potentially other adjustments such as
when a beneficiary remains in the area
but chooses to receive their care outside
of the ACO based upon where the
plurality of their primary care services
are being performed. Considering the
merits of both approaches, we believe
that the retrospective approach to
beneficiary assignment for purposes of
determining eligibility for shared
savings is compelling. We believe that
the assignment process should
accurately reflect the population that an
ACO is actually caring for, in order to
ensure that the evaluation of quality
measures is fair and that the calculation
of shared savings, if any, accurately
reflects the ACO’s success in improving
the quality and efficiency of the care
provided to the beneficiaries for which
it was actually accountable. In contrast,
as we noted previously, a prospective
approach has intrinsic inaccuracies, and
requires additional adjustments in order
to achieve the requisite level of accuracy
for purposes of the Shared Savings
Program.
In response to the November 17, 2010
RFI, of the few commenters favoring
retrospective alignment, a group of
commenters suggested the use of
retrospective alignment for determining
utilization and shared savings, but
prospective assignment for purposes of
CMS sharing beneficiary identifiable
data with ACOs. We agree that, given
appropriate safeguards for maintaining
the confidentiality of patient
information, providing ACOs with
meaningful information about their
‘‘expected assigned population’’ with the
potential to identify an ‘‘estimated
benchmark target’’ will be helpful. We
address our proposals for providing
information to ACOs to help them
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understand their patient populations
and better manage their care in section
II.C. of this proposed rule.
Therefore, we are proposing the
combined approach of retrospective
beneficiary assignment for purposes of
determining eligibility for shared
savings balanced by the provision of
aggregate beneficiary level data for the
assigned population of Medicare
beneficiaries during the benchmark
period. (As we discuss in section II.C. of
this proposed rule, we will provide
ACOs with a list of beneficiary names,
date of birth, sex, and other information
derived from the assignment algorithm
used to generate the 3-year benchmark.)
Although the assignment methodology
for the PGP demonstration was different
from the proposed Shared Savings
Program assignment methodology, when
the PGP data is modeled with the
Shared Savings Program assignment
methodology, the assigned patient
population would vary by
approximately 25 percent from year to
year. We believe that providing data on
those beneficiaries that are assigned to
an ACO in the benchmark period is a
good compromise that will allow ACOs
to have information on the population
they will likely be responsible for in
order to target their care improvements
to that population while still not
encouraging ACOs to limit their care
improvement activities to only the
subset of beneficiaries they believe will
be assigned to them in the performance
year. We believe that such a combined
approach provides the best of both
approaches while minimizing the
disadvantages of either. ACO physicians
will have the information they need to
manage their population and estimate a
target to manage towards, while they
will still be encouraged to provide highquality, efficient, and well-coordinated
services to all Medicare FFS
beneficiaries because they will not
know for sure who will be in the
assigned population. However, the
ultimate evaluation of their
effectiveness will be based on the actual
population they served. We solicit
comments on this combined approach
of retrospective beneficiary assignment
for purposes of determining eligibility
for shared savings balanced by the
provision of beneficiary data (names,
date of birth, etc.) and aggregate
beneficiary level data for the assigned
population of Medicare beneficiaries
during the benchmark period. We also
seek comment on alternate assignment
approaches, including the prospective
method of assignment.
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4. Majority vs. Plurality Rule for
Beneficiary Assignment
Section 1899(c) of the Act requires
that Medicare FFS beneficiaries be
assigned to ‘‘an ACO based on their
utilization of primary care services’’
furnished by an ACO professional who
is a physician, but it does not prescribe
the methodology for such assignment,
nor criteria on the level of primary care
services utilization that should serve as
the basis for such assignment. Rather,
the statute requires the Secretary to
‘‘determine an appropriate method to
assign Medicare FFS beneficiaries to an
ACO’’ on the basis of their primary care
utilization.
An obvious general approach is to
make such an assignment on the basis
of some percentage level of the primary
care services a beneficiary receives from
an ACO physician. The more specific
issue under such an approach is
whether to assign beneficiaries to the
ACO when they receive a plurality of
their primary care services from that
ACO, or to adopt a stricter standard
under which a beneficiary will be
assigned to an ACO only when he or she
receives a majority of their primary care
services from an ACO.
Under the PGP demonstration
beneficiaries were assigned to a practice
based on the plurality rule. By
employing a plurality standard for
primary care services, our analysis
indicates that between 78 and 88
percent of the patients seen for primary
care services at the PGP during the year
were subsequently assigned to that PGP
group. As measured by allowed charges
(evaluation and management CPT
codes), the PGP provided on average 95
percent of all primary care services
provided to the assigned patients.
Alternatively, it could be argued that
adopting a majority standard might
enhance an ACO’s sense of
responsibility for its assigned patients,
which is certainly consistent with the
general goals of the Shared Savings
Program. However, adopting a majority
standard would likely somewhat reduce
the number of beneficiaries assigned to
an ACO and more beneficiaries would
be unassigned to any ACO. On balance,
we believe that a majority rule for
assignment is too strict a standard to
employ in a system where many
Medicare beneficiaries may regularly
receive primary care services from two
or more primary care practitioners (for
example, an internal medicine
physician and a geriatric medicine
physician). As such, this standard could
undermine the development and
sustainability of ACOs. Therefore, we
are proposing to assign beneficiaries for
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purposes of the Shared Savings Program
to an ACO if they receive a plurality of
their primary care services from primary
care physicians within that ACO. We
believe that the plurality rule provides
a sufficient standard for assignment
because it ensures that beneficiaries will
be assigned to an ACO when they
receive more primary care from that
ACO than from any other provider. This
will result in a greater number of
beneficiaries assigned to ACOs, which
may enhance the viability of the Shared
Savings Program, especially in its initial
years of operation. We welcome
comments on our proposal to assign
patients based upon a plurality rule.
Additionally we would also welcome
any comments on whether there should
be a minimum threshold number of
primary care services that a beneficiary
should receive from physicians in the
ACO in order to be assigned to the ACO
under the plurality rule and if so, where
that minimum threshold should be set.
Finally, we can determine when a
beneficiary has received a plurality of
primary care services from an ACO
either on the basis of a simple service
count or on the basis of the accumulated
allowed charges for the services
delivered. The method of using a
plurality of allowed charges would
provide a greater weight to more
complex primary care services in the
assignment methodology, while a
simple service method count would
weigh all primary care encounters
equally in determining assignment. We
have previous experience with the
method of using a plurality of allowed
charges in the PGP demonstration. One
advantage of this method is that it
would not require tie-breaker rules,
since it is unlikely that allowed charges
by two different entities would be equal.
On the other hand, this method does not
necessarily assign the beneficiary to the
entity that saw the patient most
frequently, but rather to the entity that
provided the highest complexity and
intensity of primary care services.
Assignment of beneficiaries on the basis
of plurality in a simple service method
count would require tie-breaker rules for
those rare occasions when two or more
entities delivered an equal number of
services to a beneficiary. One possible
tie-breaker for such cases is to assign the
beneficiary to the ACO if it is the entity
that most recently provided primary
care services.
We propose to implement the method
of using a plurality of allowed charges
for primary care services to assign
beneficiaries to ACOs. Allowed charges
are a reasonable proxy for the resource
use of the underlying primary care
services, so the method of using a
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plurality of allowed charges assigns
beneficiaries to ACOs according to the
intensity of their primary care
interactions, not merely the frequency of
such services.
5. Beneficiary Information and
Notification
Section 1899(c) of the Act, as added
by section 3022 of the Affordable Care
Act, does not state whether beneficiaries
should be informed in any way about
the Shared Savings Program. Thus, it
does not specify any information to be
provided to beneficiaries about the
Shared Savings Program in general,
whether they are receiving services from
an ACO participant or ACO provider/
supplier, or whether they have been
assigned to an ACO for purposes of
determining that ACO’s performance
with respect to the quality standards
and its possible shared savings under
the Shared Savings Program.
As discussed previously, the term
‘‘assignment’’ as used in the statute for
purposes of this provision in no way
implies any limits, restrictions, or
diminishment of the rights of Medicare
FFS beneficiaries to exercise freedom of
choice in the physicians and other
health care practitioners from whom
they receive their services. Rather, the
statutory term ‘‘assignment’’ in this
context refers only to an operational
process by which Medicare will
determine whether a beneficiary has
chosen to receive a sufficient level of
the requisite primary care services from
a specific ACO so that the ACO may be
appropriately designated as being
accountable for that beneficiary’s care.
For example, if a beneficiary’s physician
becomes part of an ACO and the
beneficiary does not wish to receive
health care services under the ACO care
coordination and management efforts,
the beneficiary has the freedom of
choice to go to a different physician.
The continued exercise of free choice by
beneficiaries in selecting the physicians
and other health care practitioners from
whom they receive their services is thus
a presupposition of the Shared Savings
Program. The exercise of free choice,
however, can be undermined or even
nullified if beneficiaries do not possess
adequate information to assess the
possible consequences of available
choices, or to evaluate which available
options are most consistent with their
values and preferences concerning their
own health care. We therefore believe
that an important component of the
Shared Savings Program must be timely
and effective communication with
beneficiaries concerning the Shared
Savings Program, their potential
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assignment to an ACO, and what that
may mean for the beneficiaries’ care.
Furthermore, the Shared Savings
Program lays the foundation for a
beneficiary-centered delivery system
that should create a strong relationship
between beneficiaries and care
providers based, in large part, on patient
engagement in the new care system.
Such engagement would be more
difficult when beneficiaries are not
aware of the new delivery system
available from ACOs, and the possibility
of being included in the population
assigned to an ACO. In short,
transparency must be a central feature of
the Shared Savings Program.
Therefore, we intend to develop a
communications plan, including
educational materials and other forms of
outreach, to provide beneficiaries in a
timely manner with accurate, clear, and
understandable information about the
Shared Savings Program in general,
about their utilization of services
furnished by a provider or supplier
participating in an ACO, about the
possibility of their being assigned to an
ACO for quality and shared savings
purposes, and about the potential that
their health information may be shared
with the ACO, and their ability to optout of that data sharing. Accordingly,
we will update the annual Medicare
handbook to contain information about
the Shared Savings Program, ACOs, and
what receiving care from an ACO means
for the Medicare FFS beneficiary.
One limitation on the timing of the
information that we provide to
beneficiaries arises from our proposal to
assign beneficiaries to an ACO
retroactively, that is, after the end of a
performance year, on the basis of a
beneficiary’s actual primary care service
utilization during the year. It is
therefore not possible to inform
beneficiaries of their assignment to an
ACO in advance of the period in which
they may seek services from the ACO.
However, we believe that it is essential
for beneficiaries to receive some form of
advance notification that a physician or
other provider from whom they are
receiving services is participating in an
ACO. The only practical manner in
which such notification could be
provided in a timely manner is to
require ACOs to provide such
notification to beneficiaries when they
seek services from ACO providers/
suppliers. Specifically, we propose to
require ACOs to post signs in the
facilities of participating ACO
providers/suppliers indicating their
participation in the Shared Savings
Program and to make available
standardized written information to
Medicare FFS beneficiaries whom they
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serve. ACOs would provide
standardized written notice to
beneficiaries of both their participation
in the Shared Savings Program and the
potential for CMS to share beneficiary
identifiable data with ACOs when a
beneficiary receives services from a
physician on whom assignment to ACO
is based. We also plan to instruct ACOs
to supply a form allowing beneficiaries
to opt-out of having their data shared.
The form would be provided to each
beneficiary as part of their office visit
with a primary care physician, and must
include a phone number, fax or e-mail
for beneficiaries to contact and request
that their data not be shared.
Likewise, in instances where either an
ACO chooses to no longer participate in
the Shared Savings Program or we have
terminated a participation agreement
with an ACO, beneficiaries should be
made aware of this change. Thus, we are
proposing that ACOs be required to
provide beneficiaries notice in a timely
manner if they will no longer be
participating in the Shared Savings
Program. It should include the effective
date of the termination of their
agreement with us. As discussed in
section II.C. of this proposed rule, we
are also proposing to require an ACO
seeking to terminate its participation in
the Shared Savings Program to provide
us with advanced notice.
We recognize that such a requirement
could place an administrative burden on
ACOs. However, we believe that such
notification is essential to enhance
patient engagement and understanding
of their care. As discussed in section
II.B. of this proposed rule, section
1899(b)(2)(H) of the Act requires that the
‘‘ACO * * * demonstrate to the
Secretary that it meets patientcenteredness criteria specified by the
Secretary * * *.’’ We believe that
providing notice of participation in or
termination from the Shared Savings
Program to beneficiaries is essential to
the ability of beneficiaries to exercise
free choice, and therefore would be an
appropriate patient-centered criterion to
be designated by the Secretary. In
addition to notifying beneficiaries that
they are seeking services from a
provider or supplier participating in an
ACO under the Shared Savings Program,
this proposed notification will inform
beneficiaries how assignment with an
ACO is likely to affect (and not affect)
the care they receive from the providers
they have chosen. We seek comment on
the appropriate form and content of this
notification. For example, we seek
comment on the utility of informing
consumers about those objectives of the
Shared Savings Program that might have
the most impact on the beneficiary as a
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consumer of services from an ACO
professional, such as the following:
• Easing the burden on consumers to
coordinate their own care among
different providers,
• Fostering follow-up with patients as
they receive care from different
providers,
• Facilitating greater dialogue
between and among beneficiaries and
providers about how health care is
delivered, and
• Providing beneficiaries with quality
measures by which they can evaluate
the performance of their providers
compared to regional and national
norms.
We also seek comment on the most
important items to communicate to
beneficiaries about matters that will not
change under the Shared Savings
Program, including the fact that their
cost-sharing will continue to be the
same, and they remain free to seek care
from providers of their choosing.
We welcome comments not only on
our proposal to establish these
notification requirements, but also on
all matters concerning the appropriate
form and content of such notification. If
we adopt a notification requirement in
the final rule, we will take comments on
the issues such as the appropriate form
and content of such a notification into
account as we develop more detailed
instructions for ACOs on beneficiary
notification through guidance.
E. Quality and Other Reporting
Requirements
1. Introduction
As discussed in section I. of this
proposed rule, the intent of the Shared
Savings Program is to: (1) Promote
accountability to Medicare beneficiaries;
(2) improve the coordination of FFS
items and services; and (3) encourage
investment in infrastructure and
redesigned care processes to achieve
high health care quality and efficient
service delivery. In conjunction with the
Shared Savings Program and other
provisions of the Affordable Care Act,
we have adopted three goals for
improvement of the health care of
Medicare beneficiaries and, by
extension, of all Americans. These goals
include: (1) Better care for individuals;
(2) better health for populations; and (3)
lower growth in expenditures. (We
define better health care for individuals
as health care that is safe, effective,
patient-centered, timely, efficient, and
equitable, as described in the IOM’s six
aims for changing U.S. health care
delivery.) 14 This section of this
14 Committee on Quality of Health Care in
America, Institute of Medicine. Crossing the Quality
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proposed rule pertains to the first two
goals.
In this portion of the proposed
regulation, we propose: (1) Measures to
assess the quality of care furnished by
an ACO; (2) requirements for data
submission by ACOs; (3) quality
performance standards; (4) the
incorporation of reporting requirements
under section 1848 of the Act for the
Physician Quality Reporting System;
and (5) requirements for public
reporting by ACOs.
2. Proposed Measures To Assess the
Quality of Care Furnished by an ACO
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b. Considerations in Selecting Measures
We view value-based purchasing as
an important step to revamping how
care and services are paid for, moving
increasingly toward rewarding better
value, outcomes, and innovations
instead of merely volume. The Shared
Savings Program is a critical element of
our Medicare value-based purchasing
initiative. In implementing these valuebased purchasing initiatives, we seek to
meet certain common goals, as follows:
1. Use of Measures
a. General
Section 1899(b)(3)(A) of the Act,
requires the Secretary to determine
appropriate measures to assess the
quality of care furnished by the ACO,
such as measures of clinical processes
and outcomes; patient, and, wherever
practicable, caregiver experience of care;
and utilization (such as rates of hospital
admission for ambulatory sensitive
conditions). Section 1899(b)(3)(B) of the
Act requires ACOs to submit data in a
form and manner specified by the
Secretary on measures that the Secretary
determines necessary for the ACO to
report in order to evaluate the quality of
care furnished by the ACO. We believe
that the Secretary’s authority to
determine the form and manner of data
submission allows for establishing
requirements for submission of data on
measures the Secretary determines to be
appropriate for evaluating the quality of
care furnished by the ACO, without
regard to whether the Secretary has
established a specific quality
performance standard with respect to
those measures that must be met in
order to be eligible for shared savings.
We propose that an ACO be
considered to have met the quality
performance standard if they have
reported quality measures and met the
applicable performance criteria in
accordance with the requirements
detailed in rulemaking for each of the
three performance years. We further
propose to define the quality
performance standard at the reporting
level for the first year of the Shared
Savings Program and to define it based
on measure scores in subsequent
program years. We have listed the
measures we propose to use to establish
quality performance standards that
ACOs must meet for shared savings for
the first performance period in Table 1.
Quality measures for the remaining two
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2001.
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• Value-based payment systems and
public reporting should rely on a mix of
standards, processes, outcomes, and
patient experience measures, including
measures of care transitions and
changes in patient functional status.
Across all programs, we seek to move as
quickly as possible to the use of
outcome and patient experience
measures. To the extent practicable and
appropriate, these outcome and patient
experience measures should be adjusted
for risk or other appropriate patient
population or provider characteristics.
• To the extent possible, and
recognizing differences in payment
system maturity and statutory
authorities, measures should be aligned
across Medicare and Medicaid’s public
reporting and payment systems. We
seek to evolve a focused core-set of
measures appropriate to each specific
provider category that reflects the level
of care and the most important areas of
service and measures for that provider.
• The collection of information
should minimize the burden on
providers to the extent possible. As part
of that effort, we have begun and will
continuously seek to align Shared
Savings Program measures with the
methods and measures included in the
Medicare and Medicaid EHR Incentive
Programs to enable the collection and
reporting of performance information to
be a seamless part of care delivery and
the meaningful use of certified EHR
technology.
• To the extent practicable, measures
used by us should be nationally
endorsed by a multi-stakeholder
organization. Measures should be
aligned with best practices among other
payers and the needs of the end users
of the measures.
2. Scoring Methodology
• Providers should be scored on their
overall achievement relative to national
or other appropriate benchmarks. In
addition, scoring methodologies should
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consider improvement as an
independent goal.
• Measures or measurement domains
need not be given equal weight, but over
time, scoring methodologies should be
more weighted towards outcome,
patient experience and functional status
measures.
• Scoring methodologies should be
reliable, as straightforward as possible,
and stable over time and enable
consumers, providers, and payers to
make meaningful distinctions among
providers’ performance.
Consistent with these value-based
purchasing principles, our principal
goal in selecting quality measures for
ACOs is to identify measures of success
in the delivery of high-quality health
care at the individual and population
levels. We considered a broad array of
process and outcome measures and
accounted for a variety of factors in
arriving at the proposed measures,
prioritizing measures that meet the
following:
• Address the goals we previously
identified: Improving individual health
and improving the health of
populations.
• Address an array of quality
domains, priorities, and aims, including
the IOM six quality aims previously
described and the National Quality
Strategy, and other HHS priorities, such
as prevention, care of chronic illness,
treatment of high prevalence conditions
such as cardiovascular disease, patient
safety, patient and caregiver
engagement, and care coordination.
• Support the goals for the Shared
Savings Program, as stated in section
1899(a)(1) of the Act, of promoting
provider accountability for a patient
population, coordinating care furnished
under Medicare Parts A and B, and
encouraging investment in
infrastructure and redesigned care
processes for high quality and efficient
service delivery. Thus, measures should
have high impact in terms of
accountability and cost, particularly for
vulnerable populations, when
comparing beneficiary care received in
ACOs to beneficiary care received in
non-ACO Medicare FFS.
• Align with other Medicare
incentive programs such as the
Physician Quality Reporting System
(‘‘PQRS’’; formerly known as the
Physician Quality Reporting Initiative),
Electronic Prescribing Incentive
Program, Electronic Health Records
(EHR) Incentive Programs, Hospital
Inpatient Quality Reporting Program,
and also Medicaid and private sector
initiatives that align with the three-part
aim.
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• Include the quality performance
standards that ACOs must meet in order
to be eligible for shared savings, which
should be well-established, correlate
with improved patient outcomes, and be
accepted by the professional and
provider community, such as through
National Quality Forum (NQF)
endorsement.
• Are consistent across ACOs,
regardless of ACO composition.
• Offer key opportunities for
improvement in care and significantly
impact the health status and outcomes
of care for the Medicare beneficiaries
served by the ACO.
• Are limited to those that have high
impact, and/or are cross-cutting to the
extent possible, with parsimony serving
to focus clinical attention, and limiting
the burden of data collection and
reporting.
• Exhibit sensitivity to administrative
burden and seek to become less
burdensome over time.
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c. Proposed Quality Measures for Use in
Establishing Quality Performance
Standards That ACOs Must Meet for
Shared Savings
Based upon the principles described,
we are proposing 65 measures (see
Table 1) for use in the calculation of the
ACO Quality Performance Standard. We
propose that ACOs will submit data on
these measures using the process
described later in this proposed rule and
meet defined quality performance
thresholds. We propose that ACOs be
required to report quality measures and
meet applicable performance criteria, as
defined in rulemaking, for all 3 years
within the 3-year agreement period to be
considered as having met the quality
performance standard. Specifically, for
the first year of the program, we propose
for the quality performance standard to
be at the level of full and accurate
measures reporting; for subsequent
years, we propose the quality
performance standard be based on a
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measures scale with a minimum
attainment level as described in section
II.E.4 of this proposed rule.
ACOs that do not meet the quality
performance thresholds for all proposed
measures would not be eligible for
shared savings, regardless of how much
per capita costs were reduced.
Specifically, as discussed in section
II.H. of this proposed rule, in those
instances where an ACO fails to meet
the minimum attainment level for 1 or
more domains, we propose to give the
ACO a warning and to re-evaluate the
following year. If the ACO continues to
underperform on the quality
performance standards in the following
year, the agreement will be terminated.
We also propose that if an ACO fails to
report 1 or more measures, we would
send the ACO a written request to
submit the required data by a specified
date and to provide a reasonable written
explanation for its delay in reporting the
required information. If the ACO fails to
report by the requested deadline and
does not provide a reasonable
explanation for delayed reporting, we
would immediately terminate the ACO
for failing to report quality measures.
ACOs that exhibit a pattern of
inaccurate or incomplete reporting or
fail to make timely corrections following
notice to resubmit may be terminated
from the program. We note that since
meeting the quality standard is a
condition for sharing in savings, the
ACO would be disqualified from sharing
in savings in each year in which it
underperforms. Termination from the
Shared Savings Program is discussed
further in sections II.H and II.C. of this
proposed rule.
In addition to categorizing each of the
proposed measures into the goals of
better care for individuals and better
health for populations, Table 1 includes
the domain each of the proposed
measures addresses, the measure title, a
brief description of the data the measure
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captures, applicable Physician Quality
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Programs information, the measure
steward or, if applicable, NQF measure
number, the proposed method of data
submission for each measure, and the
Measure Type. Under Measure Type, we
have listed Patient Experience of Care,
Process, or Outcome, consistent with
the domains proposed in the Hospital
Value Based Purchasing rule (76 FR
2457), for each of the proposed Shared
Savings Program quality measures.
In an effort to provide focus to ACO
quality improvement activity, we have
identified 5 key domains within the
dimensions of improved care and
improved health that we propose will
serve as the basis for assessing,
benchmarking, rewarding, and
improving ACO quality performance.
These 5 domains are as follows:
• Better Care for Individuals:
++ Patient/Caregiver Experience
++ Care Coordination
++ Patient Safety
• Better Health for Populations:
++ Preventive Health
++ At-Risk Population/Frail Elderly
Health
We note that while many of the
proposed measures have NQF
endorsement or are currently used in
other CMS quality programs, the
specifications for some of the proposed
measures will need to be refined in
order to be applicable to an ACO
population. However, we propose to
align the quality measures specifications
for the Shared Savings Program with the
measures specifications used in our
existing quality programs to the extent
possible and appropriate for purposes of
the Shared Savings Program. We plan to
make the specifications for the proposed
measures available on our Web site
prior to the start of the Shared Savings
Program.
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Information on Physician Quality
Reporting System measures are
available at: https://www.cms.gov/pqri/.
Information on EHR Incentive Program
measures are available at: https://
www.cms.gov/EHRIncentivePrograms/.
Information on quality measures used
by the Hospital Inpatient Quality
Reporting Program are available at:
https://www.cms.gov/
HospitalQualityInits/
08_HospitalRHQDAPU.asp.
As illustrated in the ‘‘Method of Data
Submission’’ column of Table 1, we
propose to calculate results for the first
program year measures via claims, the
Group Practice Reporting Option
(GPRO) data collection tool, as
discussed in section II.E.4. of this
proposed rule, and survey instruments.
The ACO GPRO tool would be a new
tool based on the data collection tool
currently used in the Physician Quality
Reporting System (formerly known as
the Physician Quality Reporting
Initiative) group practice reporting
option (GPRO) and Physician Group
Practice (PGP) demonstration.
In subsequent program years through
additional rulemaking, we would expect
to refine and expand the ACO measures
to enhance our ability to assess the
quality of care furnished by ACOs
participating in the Shared Savings
Program and expand measures reporting
mechanisms to include those that are
directly EHR-based. Specifically, we
expect to expand the measures through
future rulemaking to include other
highly prevalent conditions and areas of
interest, such as frailty, as well as
measures of caregiver experience. In
addition to ambulatory measures, we
would expect to add measures of
hospital-based care and quality
measures for care furnished in other
settings, such as home health services
and nursing homes. To the extent
consistent with the Shared Savings
Program requirements under section
1899 of the Act, we also anticipate the
ACO quality measures will evolve over
time in an effort to achieve our quality
program alignment goal of developing a
single quality measure set that could be
used by ACOs operating across a wide
variety of payers, including those
dealing with Medicaid, the Children’s
Health Insurance Program (CHIP), and
Special Needs Plans.
We invite comments on the
implication of including or excluding
any proposed measure or measures in
the calculation of the ACO Quality
Performance Standard. Commenters
may suggest variations or substitutions
that are substantially equivalent to the
proposed measures. However, without
future rulemaking, we cannot consider
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measures that do not substantially cover
the same patient populations, processes,
or outcomes addressed by the existing
measures outlined in this proposed rule.
We invite comment on whether the list
of proposed measures should be
narrowed, and also invite comments on
whether any of the measures we
proposed in Table 1 for calculating the
ACO Quality Performance Standard
should be excluded for scoring purposes
and/or instead be considered for quality
monitoring purposes only. Finally, we
also seek comment on a process for
retiring or adjusting the weights of
domains, modules, or measures over
time.
3. Requirements for Quality Measures
Data Submission by ACOs
a. General
Under section 1899(b)(3)(B) of the
Act, ACOs are required to submit data
in a form and manner specified by the
Secretary on measures the Secretary
determines necessary for the ACO to
report in order to evaluate the quality of
care furnished by the ACO. Most of the
proposed measures identified in Table 1
can be derived from CMS systems and
calculated for the assigned patient
population the ACO serves. Most of the
measures are consistent with those
reported for the Physician Quality
Reporting System, others will rely on
eRx and HITECH program data, and
some may rely on Hospital Compare or
the Centers for Disease Control and
Prevention National Healthcare Safety
Network data. However, we recognize
that there are a number of limitations
associated with claims-based reporting,
since the claims processing system was
designed for billing purposes and not
for the submission of quality data. For
instance, measures dealing with
laboratory results are not conducive to
claims-based reporting, since claims
typically include diagnosis and
procedure codes but not specific test
results. For this reason, we propose to
make available a CMS-specified data
collection tool and a survey tool for
certain proposed measures (that is,
those measures in Table 1 where the
proposed method of data submission is
listed as ‘‘GPRO’’).
We also propose that for some
measures ACOs collect data via survey
instruments. As noted previously, we
plan to continually align the ACO
reporting requirements with those
required for the EHR Incentive Program
and leverage the infrastructure and
measures specifications being
developed for that program. We propose
that during the year following the first
performance period, each ACO would
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be required to report via the GPRO tool,
as applicable, the proposed quality
measures listed in Table 1 with respect
to services furnished during the
performance period. We propose that
we would derive the claims-based
measures from claims submitted for
services furnished during the first
performance period, which therefore
would not require any additional
reporting on the part of ACO
professionals. Survey data would also
reflect care received during the first
performance period. For future
performance periods, we intend to use
rulemaking to update the quality
measure requirements and mechanisms.
We welcome comments on the
proposed data submission requirements.
We also seek comment on whether
alternative data submission methods
should be required or considered, such
as limiting the measures to claims-based
and survey-based reporting only.
b. GPRO Tool
In 2010, 36 large group practices and
integrated delivery systems used the
GPRO tool to report 26 quality measures
for an assigned patient population
under the Physician Quality Reporting
System. The GPRO tool affords a key
advantage in that it is a mechanism
through which beneficiary laboratory
results and other measures requiring
clinical information can be reported to
us. The tool would allow ACOs to
submit clinical information from EHRs,
registries, and administrative data
sources required for measurement
reporting. The tool reduces the
administrative burden on health care
providers participating in ACOs by
allowing them to tap into their existing
Information Technology (IT) tools that
support data collection and health care
provider feedback, including at the
point of care. We propose that the
existing GPRO tool be built out, refined,
and upgraded to support clinical data
collection and measurement reporting
and feedback to ACOs under the Shared
Savings Program.
For the measures with ‘‘GPRO’’ listed
as the method of data collection in
Table 1, we plan to determine a sample
for each domain or measure set within
the domain using a sampling
methodology modeled after the
methodology currently used in the 2011
Physician Quality Reporting System
GPRO I, as described later in the
document. Assigned beneficiaries, for
purposes of the GPRO tool, would be
limited to those Medicare FFS
beneficiaries assigned to the ACO, as
discussed in Section II.D.
For the measures with ‘‘GPRO’’ listed
as the method of data collection in
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Table 1, we also plan to provide each
ACO with access to a database (that is,
the GPRO data collection tool) that will
include a sample of its assigned
beneficiary population and the GPRO
quality measures listed in Table 1. We
plan to pre-populate the data collection
tool with the beneficiaries’ demographic
and utilization information based on
their Medicare claims data. The ACO
would be required to populate the
remaining data fields necessary for
capturing quality measure information
on each of the beneficiaries.
Identical to the sampling method used
in the 2011 Physician Quality Reporting
System GPRO I, we plan to require that
the random sample for measures
reported via ACO GPRO must consist of
at least 411 assigned beneficiaries per
measure set/domain. If the pool of
eligible, GPRO assigned beneficiaries is
less than 411 for any measure set/
domain, then we plan to require the
ACO to report on 100 percent, or all, of
the assigned beneficiaries. For each
measure set/domain within the GPRO
tool, the ACO would be required to
report information on the assigned
beneficiaries in the order in which they
appear consecutively in the ACO’s
sample.
Some GPRO measures will not rely on
beneficiary data but rather on ACO
attestation. GPRO measures relying on
attestation include those in the Care
Coordination domain that pertain to
HITECH Meaningful Use, the Electronic
Prescribing Incentive Program, and
patient registry use. We plan to validate
GPRO attestations through CMS data
from the EHR Incentive Program and
Electronic Prescribing Incentive
Program.
For the other measures, that we
propose be reported via the GPRO tool,
we propose to retain the right to validate
the data entered into the tool. In the
event we were to audit the data entered
into the GPRO tool, we propose to do so
via a data validation process based on
the one used in phase I of the PGP
demonstration, as described later in the
document.
In the GPRO audit process, we plan to
abstract a random sample of 30
beneficiaries previously abstracted for
each of the quality measure domains/
measure sets. The audit process would
include up to three phases, depending
on the results of the first two phases.
Although each sample would include 30
beneficiaries per domain, only the first
eight beneficiaries’ medical records
would be audited for mismatches during
the first phase of the audit. A mismatch
represents a discrepancy between the
numerator inclusions or denominator
exclusions in the data submitted by the
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ACO and our determination of their
appropriateness based on supporting
medical records information submitted
by the ACO. If there are no mismatches,
the remaining 22 of the 30 beneficiaries’
records would not be audited. If there
are mismatches, the second phase of the
audit would occur, and the other 22
beneficiaries’ records would be audited.
A third phase would only be undertaken
if mismatches are found in more than 10
percent of the medical records in phase
two. If a specific error is identified and
the audit process goes to Phase 3, which
involves corrective action, we propose
to first provide education to the ACO on
the correct specification process and
provide the opportunity to correct and
resubmit the measure(s) in question. If,
at the conclusion of the third audit
process the mismatch rate is more than
10 percent, we propose that the ACO
will not be given credit for meeting the
quality target for any measures for
which this mismatch rate still exists. We
note that the failure to report quality
measure data accurately, completely
and timely (or to timely correct such
data) may subject the ACO to
termination or other sanctions, per the
Monitoring section of this proposed
rule.
We invite comment on the proposed
quality data submission requirements
and on the administrative burden
associated with reporting.
c. Certified EHR Technology
In July 2010, HHS published final
rules for the EHR Incentive Programs.
Included within the final regulations
were certain clinical quality measures
for which eligible professionals and
eligible hospitals are responsible. We
have noted in Table 1, the proposed
Shared Savings Program quality
measures currently included in the EHR
Incentive Programs and will continue to
further align the measures between the
two programs. Given that we have
proposed in Section II.E.6 that at least
50 percent of an ACO’s PCPs are
‘‘meaningful EHR users’’ as that term is
defined in 42 CFR 495.4 by the start of
the second Shared Savings Program
performance year in order to continue
participation in the Shared Savings
Program, our intent is to develop the
capability of the GPRO web-based tool
to interface with EHR technology, such
that EHR data could directly populate
the ACO GPRO tool with the required
quality data. As we intend to further
align both the Shared Savings Program
and EHR incentive program through
subsequent rulemaking, we anticipate
that certified EHR technology (including
certified EHR modules capable of
reporting clinical quality measures) will
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be an additional measures reporting
mechanism used by ACOs under the
Shared Savings Program for future
program years.
4. Quality Performance Standards
a. General
Before an ACO can share in any
savings created, it must demonstrate
that it is delivering high quality care.
Thus, a calculation of the quality
performance standard will indicate
whether an ACO has met the quality
performance goals that would deem it
eligible for shared savings. As discussed
previously in section II.E.3 of this
proposed rule, we propose to use the 65
measures in Table 1 to establish the
quality performance standards that
ACOs must meet in order to be eligible
for shared savings.
We considered two alternative
options for establishing quality
standards: Rewards for better
performance, and a minimum quality
threshold for shared savings. The
performance score approach rewards
ACOs for better quality with larger
percentages of shared savings. The
threshold approach ensures that ACOs
exceed minimum standards for the
quality of care, but allows full shared
savings if ACOs meet the minimum. We
propose the performance score approach
and seek comment on the threshold
approach.
b. Option 1—Performance Scoring
Under the first option, we would use
quality performance standards to arrive
at a total performance score for an ACO.
We would organize the measures by
domain, as discussed in section II.E.5.b.
of this proposed rule. The performance
on each measure will be scored, as
discussed in section II.E.5.c. of this
proposed rule. The scores for the
measures will be rolled up into a score
by each domain as discussed in section
II.E.5.d. of this proposed rule. ACOs
will receive performance feedback at
both the individual measure and
domain level. The percentage of points
earned for each domain will be
aggregated using the weighting method
discussed in section II.E.5.d. of this
proposed rule to arrive at a single
percentage that will be applied to
determine the quality sharing rate for
which the ACO is eligible. The
aggregated domain scores will
determine the ACO’s eligibility for
sharing up to 50 percent of the total
savings generated by the ACO under the
one-sided model or 60 percent of the
total savings generated by the ACO
under the two-sided risk model
discussed in Section II. G, Two-Side
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(1) Measure Domains and Measures
Included in the Domains
The 65 quality performance standard
measures in Table 1 are subdivided into
5 domains, as discussed in section
II.E.3.c. of this proposed rule. The
domains include: (1) Patient/Caregiver
Experience; (2) Care Coordination; (3)
Patient Safety; (4) Preventive Health; (5)
At-Risk Population/Frail Elderly Health.
The At-Risk Population Care domain
would include the following chronic
diseases: Diabetes mellitus (DM); heart
failure (HF); coronary artery disease
(CAD); hypertension; and chronic
obstructive pulmonary disorder (COPD).
The measures from Table 1 that are
included in each domain are as
indicated in Table 2.
(2) Methodology for Calculating a
Performance Score for Each Measure
Within a Domain
established using the most currently
available data source and most recent
available year of benchmark data prior
to the start of the Shared Savings
Program annual agreement periods. We
would determine Medicare FFS rates by
pulling a data sample and modeling the
measures. For MA rates, we would
check the distribution from annual MA
quality performance data and set the
benchmark accordingly. Furthermore,
since MA quality performance rates
utilize both claims and clinical data, we
propose to use those rates when they are
available.
Benchmark levels for each of the
measures included in the quality
performance standard would be made
available to ACOs, prior to the start of
the Shared Savings Program and each
annual performance period thereafter,
so ACOs will be aware of the
benchmarks they must achieve to
receive the maximum quality score. In
future program years, we anticipate that
actual ACO performance will be used to
update the benchmarks. As discussed in
section II.H of this proposed rule, if an
ACO fails to meet quality performance
standard during a performance year
(that is, fails to meet, the minimum
attainment level for one or more
domain(s)), we propose to give the ACO
a warning, provide an opportunity to
resubmit, and reevaluate the ACO’s
performance the following year. If the
ACO continues to significantly underperform, the agreement may be
terminated. We further propose that
ACOs that exhibit a pattern of
inaccurate or incomplete reporting or
fail to make timely corrections following
notice to resubmit may be terminated
from the program.
srobinson on DSKHWCL6B1PROD with PROPOSALS2
We propose that an ACO will receive
a performance score on each measure
included in Table 1. For the first year
of the Shared Savings Program, these
scores would be for informational
purposes, since we propose to set the
quality performance standard at the
reporting level. We propose setting
benchmarks for each measure using
Medicare FFS claims data, MA quality
performance rates, or, where
appropriate, the corresponding percent
performance rates that an ACO will be
required to demonstrate. For each
measure, we propose to set a
performance benchmark and a
minimum attainment level as defined in
Table 3. The benchmarks would be
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Model. We also discuss our proposal to
set the quality performance standard in
the first year of the Shared Savings
Program at the reporting level and set
the standard at a higher level in
subsequent years in section II.E.5.e. of
this proposed rule.
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2 composite measures. The intent of all
or nothing scoring is to signal to
providers that failing to perform any
element of a process is unacceptable
and will result in a ‘‘zero’’ score for
quality for that measure. We believe that
incorporating all or nothing scoring
concepts into the ACO quality
performance standard would provide
greater insight into the use of these
methodologies, drive ACOs to
aggressively improve their population’s
health, and encourage future
development of composite measures.
However, we also recognize that all or
nothing scoring implies that all
beneficiaries can and should receive the
indicated care process, which may not
necessarily be appropriate for all
beneficiaries in the Medicare population
given the difficulty in attaining targets
for individuals with multiple chronic
conditions and complications that may
not be adequately addressed in
denominator exclusions. Therefore, in
addition to scoring the diabetes and
CAD composites, we also propose
scoring the sub measures within the
diabetes and CAD composites
individually.
Measure #24 is a hospital acquired
conditions (HACs) composite, in which
we propose a summation of the events
included within the measure and
attributing the rate to the same scale
used for other measures described in
Table 3. We do not propose all or
nothing scoring for this composite, since
the HACs are rare events. Because the
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HACs are rare events, we believe that
grouping them into one measure will
make the measure more meaningful for
ACOs, which will have smaller
populations and, therefore, should have
even fewer HAC events than a hospital
would experience for its total
population outside of the Shared
Savings Program. We also believe
grouping the HACs into one measure
reduces the HACs’ impact on the ACO’s
overall quality performance score. We
intend to post performance rates for the
final measures set, including the
applicable benchmarks, on the CMS
Web site prior to the start of the first
performance period.
(3) Methodology for Calculating a
Performance Score for Each Domain
Similar to our proposal for setting a
quality standard for each individual
measure at the reporting level in the
first program year, we also propose
setting a quality standard for each
domain at the reporting level. For
subsequent program years, we plan to
calculate the percentage of points an
ACO earns for each domain after
determining the points earned for each
measure. We plan to divide the points
earned by the ACO across all measures
in the domain by the total points
available in that particular domain.
Each domain would be worth a predefined number of points based on the
number of individual measures in the
domain, as shown in Table 4.
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We propose that performance below
the minimum attainment level would
earn zero points for that measure under
both the one-sided and two-sided risk
models. Performance equal to or greater
than the minimum attainment level but
less than the performance benchmark
shall receive points on a sliding scale
based on the level of performance, for
those measures in which the points
scale applies. Table 3 represents the
approach that we are currently
considering. We also are considering
setting the initial minimum attainment
level for both the one-sided and twosided shared savings models at 30
percent or the 30th percentile of
Medicare FFS or the MA rate,
depending on what performance data
are available.
Measures 35 and 52 in Table 1
include diabetes and coronary artery
disease composite measures in which
we propose ‘‘all or nothing’’ scoring. We
propose that measures designated as all
or nothing measures receive the
maximum available points if all criteria
are met and zero points if at least one
of the criteria are not met. We define ‘‘all
or nothing’’ scoring to mean all of the
care process steps and expected
outcomes for a particular beneficiary
with the target condition must be
achieved to score positively. This means
all 5 submeasures within the diabetes
composite and all 5 submeasures within
the CAD composite would need to be
reported in order to earn points for these
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As illustrated in Table 4, a maximum
of 2 points per measure could be earned
under both the one-sided and two-sided
model based on the ACO’s performance.
However, the total potential for shared
savings will be higher under the twosided model, since the maximum
potential shareable savings based on
quality performance is 60 percent of the
savings generated, compared to 50
percent under the one-sided model.
That is, full and accurate reporting of
the quality measures in the first year of
the Shared Savings Program will result
in an ACO earning 60 or 50 percent of
shareable savings, depending on
whether the ACO is in the two-sided or
one-sided model. For future program
years, the percent of potential shareable
savings will vary on the ACO’s
performance on the measures as
compared with the measure
benchmarks.
For example, the preventive health
domain has 9 measures and would be
worth a maximum of 18 points (that is,
9 measures × 2 points equals 18 quality
points). We propose the sliding scale in
Table 3 for determining points earned
for each measure. As mentioned
previously, we propose calculating the
percentage of points an ACO earns for
each domain by dividing the points
earned by the total points available,
yielding a percentage. For example, if an
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ACO earns 16.2 out of 18 points in the
preventive health domain, the ACO
earned 90 percent of the points for the
preventive health domain (16.2 divided
by 18 equals .90). Assuming the ACO is
operating under the two-sided shared
savings model and earns 90 percent of
the quality performance points across
all five domains and generates shared
savings, it would receive 90 percent of
the ACO’s share of the savings or 54
percent of the total savings generated.
That is, achieving 90 percent of the
potential 60 percent of shared savings
an ACO can earn under the two-sided
model, means the ACO could earn 54
percent of the total savings generated.
Under the one-sided model, achieving
90 percent of the potential 50 percent of
shared savings, means the ACO could
earn 45 percent of the shareable savings
generated.
Under both the one-sided and twosided shared savings models, the quality
measures domain scoring methodology
treats all domains equally regardless of
the number of measures within the
domain. We believe the key benefit of
weighting the domains equally is that it
does not create a preference for any one
domain, which we believe is important
as we expect ACOs to vary in
composition, and, as a result, to place
more emphasis on different domains.
We also considered weighting the
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domains to emphasize priority
conditions or areas in order to
emphasize (or de-emphasize) certain
measures that are more difficult (or
easy) to achieve without needing to
change the scoring methodology. This
method would require judgment about
which domains are more important than
others, which may not be appropriate.
Equal weighting contains an implicit
judgment that domains such as patient/
caregiver experience of care and patient
safety are equally important to the
quality of care. Accordingly, we believe
ACOs should seek to address all aspects
of patient care in order to improve the
overall quality of care under the
Medicare program. Furthermore, we
want to encourage a diverse set of ACOs
and believe that emphasizing certain
domains over others would encourage a
certain type of ACO to participate but
discourage other types from
participating.
We propose aggregating the quality
domain scores into a single overall ACO
score which would be used to calculate
the ACOs final sharing rate for purposes
of determining shared savings or shared
losses as described in section II.F. of
this proposed rule. All domain scores
for an ACO would be averaged together
equally to calculate the overall quality
score that would be used to calculate
the ACO’s final sharing rate.
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We also propose that ACOs must
report completely and accurately on all
measures within all domains to be
deemed eligible for shared savings
consideration. We believe this is
important as it requires ACOs to address
all domains and be accountable across
the continuum of care. If the ACO
demonstrates sufficient cost savings in
addition to meeting the quality
performance requirements, the ACO
would be deemed eligible for shared
savings. We believe that this
methodology provides a sufficient
incentive for quality improvement
targeted to specific domains and allows
ACOs of varying compositions, which
may be stronger in some domains than
others, to receive some level of shared
savings. In addition to this proposed
domain-based scoring methodology, we
considered several other options for
assessing the quality performance of
ACOs. We considered scoring measures
individually under a method that would
weight all measures equally. Each
measure would be worth the maximum
points available as described previously
for a total maximum possible points for
each ACO. This system would avoid
overweighting or underweighting
measures due to the number of
measures in a domain. We also
considered weighting quality measures
by their clinical importance. More
important quality measures would
account for a greater proportion of
shared savings. Outcome measures such
as hospital-acquired infections and
readmissions would be worth more than
process measures. This would avoid
overweighting or underweighting
measures due to their domain, and
account for clinical importance.
However, we did not think either of
these approaches would be consistent
with a larger measurement strategy of
driving better health for populations
and better care for individuals overall
for the ACO beneficiary population,
since we believe population health is
better assessed across domains that
encompass a variety of measures that
apply to beneficiaries with different
needs.
(4) The Quality Performance Standard
Level
We propose to set the quality
performance standard of the first year of
the Shared Savings Program at the
reporting level. That is, under the onesided model, we propose that an ACO
would receive 50 percent of shared
savings (provided that the ACO realizes
sufficient cost savings under the
methodology described in the Shared
Savings Determination section of this
proposed rule) based on 100 percent
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complete and accurate reporting on all
quality measures. Similarly, we propose
that under the two-sided risk model,
ACOs would receive 60 percent of
shared savings (provided that the ACO
realizes sufficient cost savings under the
methodology described in the section
II.G. of this proposed rule) based on 100
percent complete and accurate reporting
on all quality measures. We believe
setting the quality performance standard
for the first year of the Shared Savings
Program at full and accurate reporting
allows ACOs to ramp up, invest in their
infrastructure, engage ACO providers/
suppliers, and redesign care processes
to capture and provide data back to their
ACO providers/suppliers to transform
care at the point of care. It also would
provide CMS with the opportunity to
learn about the process, establish and
refine benchmarks on ACO reported
data, and establish improvement targets
using data reporting for the first
performance year. Setting the quality
performance standard at the reporting
level is also consistent with other valuebased purchasing programs that have
started out initially as pay for reporting
programs.
Via future rulemaking, we plan to
raise the quality performance standard
requirements beginning in the second
program year, when actual performance
on the reported measures would be
considered in determining whether an
ACO is eligible to receive any shared
savings (provided, that the ACO realizes
cost savings under the methodology
described in the Shared Savings
Determination section of this proposed
rule). We believe this approach is
consistent with section 1899(b)(3)(C) of
the Act, which requires that the
Secretary ‘‘seek to improve the quality of
care furnished by ACOs over time by
specifying higher standards, new
measures, or both for the purposes of
assessing such quality of care.’’
c. Option 2: Quality Threshold
Under the second option, we would
establish a minimum quality threshold
for participating ACOs. If an ACO
exceeded the quality threshold, it would
retain the full shared savings percentage
attributable to quality under this
proposed rule (50 percent for one-sided
risk, and 60 percent for two-sided risk).
If an ACO did not meet the minimum
quality standards in a performance year,
it would not be eligible for shared
savings. Furthermore, as discussed in
section II.H. of this proposed rule and
with respect to the performance
standards option, if an ACO that fails to
meet the minimum threshold during a
performance year, we propose to give
the ACO a warning, an opportunity for
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19597
correction, and follow the termination
process described in the Monitoring
section if the ACO continues to
underperform.
(1) Minimum Quality Threshold
Alternatively, we could establish the
minimum quality threshold using the
same set of quality measures and
domains outlined in Table 1. We would
also use the benchmarks for
performance described in Table 3,
established using claims data from FFS
Medicare or the Medicare Advantage
program. The minimum quality
threshold would be performance at or
above the 50th percentile (on the
performance standards described in
Table 3) for each domain: patient/
caregiver experience; care coordination;
patient safety; preventive health; and atrisk population/frail elderly. If an ACO
meets these thresholds, it would be
eligible for the full 50 percent of shared
savings attributable to quality for those
participating in the one-sided model,
and the full 60 percent for those
participating in the two-sided model. If
an ACO failed to meet this threshold, it
would not be eligible for shared savings.
We expect that the quality threshold
will increase over time in future
rulemaking, under the requirement to
improve the quality of care furnished by
the ACO under section 1899(b)(3)(C) of
the Act. We solicit comment on this
approach and the appropriate threshold
level, and on the pros and cons of the
minimum threshold approach.
(2) Considerations in Establishing a
Quality Threshold
The quality threshold option has
advantages and disadvantages compared
with the performance standard option.
Under the performance standard option,
an ACO could receive rewards for
higher quality based on outcomes in one
or two domains (for example, patient/
caregiver experience and preventive
care), while having very low quality in
others (for example, patient safety). This
is true for individual measures (for
example, healthcare-acquired
infections) as well. Setting a minimum
threshold ensures that all ACOs meet
basic standards on all quality measures,
with a special emphasis on patient
safety. An ACO’s quality outcomes may
vary from year to year due to factors
outside of its control, meaning that
performance-based standards could
reward ACOs due to random variability.
A threshold established at a basic level
of quality acknowledged to be
minimally necessary presents less of a
risk of being triggered due to random
variation, as opposed to truly poor
performance. Finally, for ACOs meeting
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the threshold, their shared savings
percentage attributable to quality would
be fixed and certain. This would
increase incentives, achieve savings,
and present more certainty on potential
investment returns for organizations
considering whether or not to become
ACOs.
A quality threshold also presents
disadvantages. Under this model, once
an ACO is certain that it has met the
minimum threshold, there is no
incentive to continue improving quality;
in effect, the quality incentives would
be the same as under traditional FFS.
ACOs may even have an incentive to
reduce quality to just above the
minimum. Additionally, an ACO would
not be rewarded for improving quality
outcomes on specific measures once it
was confident that the minimum was
exceeded.
In addition to proposing these two
options, we also considered establishing
performance standards for the
overarching goals (of improving health
care for individuals and populations) or
a single performance standard to
measure overall ACO performance.
However, we believe that such
aggregated scores may not be
meaningful or useful for the ACO, since
the general goals of improving health for
individuals and populations are not as
actionable as, for instance, a specific
goal of lowering patients’ LDL
cholesterol levels. For the patient
experience domain measures, we also
considered weighting more heavily the
responses of beneficiaries who have
sought care with the ACO providers
longer than the responses of those who
are newer to the ACO providers. Finally,
we considered an option that would
permit the ACO to satisfy the quality
performance standards based on peer to
peer benchmarking. Under this
approach the quality measure
benchmarks would be set based on all
ACOs’ performance during the year.
However, the main reason we did not
propose this option is that, for measures
in which most ACOs achieve high
performance levels, minor changes in
performance could determine whether
an ACO achieves the performance
benchmark. Thus, there would be little
incentive to improve quality beyond the
level necessary to share in savings.
Additionally, our proposed approach
enables us to reward improvement over
the minimum attainment level by
allowing the ACO to share in greater
savings as they improve over time.
We also considered permitting ACOs
to report a subset of the measures in
Table 1, based on their level of
readiness to participate in the Shared
Savings Program. ACOs seeking to
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participate in the Shared Savings
Program may vary with respect to their
readiness to function in the Shared
Savings Program, with respect to their
organizational and systems capacity and
structure. Accordingly, some ACOs
might more quickly be able to
demonstrate quality improvements and
savings than will others. However,
consistent with the overall goals of the
Shared Savings Program discussed in
section I. of this proposed rule, we
believe that ACOs participating in the
Shared Savings Program should seek to
improve quality across a variety of
measures addressing a range of
domains, not only for those areas in
which they are currently able or
comfortable to report, hence our
proposal to require 100 percent
reporting for the measures in Table 1 to
satisfactorily meet the quality
performance requirements under the
Shared Savings Program
We propose the performance scoring
option and invite comment on this
option as well as the quality threshold
option. Within these options, we seek
comment on the appropriateness of
weighting all domains equally in
determining an ACO’s quality
performance or whether certain
domains and/or specific measures
should be weighted more heavily. We
also invite comment on alternatives that
would blend these two approaches. For
example, under the two-sided model,
allowing ACOs that generate savings to
increase their share of savings with
higher quality scores (Option 1) but
using a threshold approach (Option 2)
when calculating losses so that higher
quality does not reduce an ACO’s share
of any losses. Such an approach would
have the effect of essentially applying a
minimum sharing rate for losses (for
example, 50 percent) and could
appropriately reflect the goal of the
Shared Savings Program to reward high
quality and efficient care, by providing
a greater reward when high quality care
is also efficient and less relief for high
quality care that is not efficient.
Alternatively, the threshold option
could be utilized in the two-sided
model so that if the threshold score for
the two-sided model resulted in 60%
shared savings, it would also result in
60 percent shared losses, creating a
symmetrical two-sided model. Another
example of a blended approach would
be to use the threshold approach
(Option 2) for the first 3 years of the
Shared Savings Program and then, as
experience is gained and measures are
further aligned, transition to
performance scoring (Option 1). We also
invite comment on the proposal to set
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the quality performance standard of the
first program year at the reporting level
and to raise the standard to reflect
performance in subsequent years. We
also invite comment on the proposed
quality measures scoring methodologies
under the one-sided and two-sided risk
models. In addition, we invite comment
on our proposal to have all quality
measures listed in Table 1 required of
all ACOs, and the alternative under
which ACOs would be required to only
report a subset of the measures in Table
1, based on their level of readiness for
the Shared Savings Program.
5. Incorporation of Other Reporting
Requirements Related to the Physician
Quality Reporting System and
Electronic Health Records Technology
Under Section 1848 of the Act
Medicare provides multiple incentive
payment options for providers to report
and use clinical information more
proactively in their practices. The
Affordable Care Act gives the Secretary
authority to incorporate reporting
requirements and incentive payments
from these programs into the Shared
Savings Program, and to use alternative
criteria to determine if payments are
warranted. Specifically, section
1899(b)(3)(D) of the Act affords the
Secretary discretion to ‘‘* * *
incorporate reporting requirements and
incentive payments related to the
physician quality reporting initiative
(PQRI), under section 1848, including
such requirements and such payments
related to electronic prescribing,
electronic health records, and other
similar initiatives under section 1848
* * *’’ and permits the Secretary to ‘‘use
alternative criteria than would
otherwise apply under section 1848 for
determining whether to make such
payments.’’ Under this authority, we
propose to incorporate certain reporting
requirements and payments related to
the Physician Quality Reporting System
into the Shared Savings Program for
‘‘eligible professionals’’ within an ACO.
Under section 1848(k)(3)(B) of the Act,
the term ‘‘eligible professional’’ means
any of the following: (1) A physician; (2)
a practitioner described in section
1842(b)(18)(C) of the Act; (3) a physical
or occupational therapist or a qualified
speech-language pathologist; or (4) a
qualified audiologist.
We propose to incorporate a
Physician Quality Reporting System
group practice reporting option (GPRO)
under the Shared Savings Program and
further propose that the eligible
professionals that are ACO participant
providers/suppliers would constitute a
group practice for purposes of
qualifying for a Physician Quality
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Reporting System incentive under the
Shared Savings Program. Specifically,
eligible professionals would be required
to submit data through the ACO on the
quality measures proposed in Table 1
using the GPRO tool and methodology
described in section II.E.3. of this
proposed rule to qualify for the
Physician Quality Reporting System
incentive under the Shared Savings
Program. We propose that the ACO
would report and submit data on behalf
of the eligible professionals in an effort
to qualify for the Physician Quality
Reporting System incentive as a group
practice; that is, eligible professionals
within an ACO would qualify for the
Physician Quality Reporting System
incentive as a group practice, and not as
individuals. In addition, we propose a
calendar year reporting period from
January 1 through December 31, for
purposes of the Physician Quality
Reporting System incentive under the
Shared Savings Program.
With regard to the requirements for
satisfactory reporting for purposes of
earning the Physician Quality Reporting
System incentive under the Shared
Savings Program, we propose to
incorporate certain aspects of the
criteria for satisfactory reporting under
the 2011 Physician Quality Reporting
System GPRO I option (75 FR 73506),
with a few modifications. In particular,
we propose the following criteria for
satisfactory reporting for purposes of the
Physician Quality Reporting System
incentive for the first performance
period under the Shared Savings
Program:
• ACOs, on behalf of its EPs, would
need to report on all measures included
in the data collection tool;
• Beneficiaries will be assigned to the
ACO using the methodology described
in the Assignment section of this
proposed rule. As a result, the GPRO
tool would be populated based on a
sample of the ACO-assigned beneficiary
population. ACOs would need to
complete the tool for the first 411
consecutively ranked and assigned
beneficiaries in the order in which they
appear in the group’s sample for each
domain, measure set, or individual
measure if a separate denominator is
required such as in the case of
preventive care measures which may be
specific to one sex. If the pool of eligible
assigned beneficiaries is less than 411,
the ACO would report on 100 percent of
assigned beneficiaries for the domain,
measure set, or individual measure.
• The GPRO tool will need to be
completed for all domains, measure
sets, and measures described in Table 1.
Accordingly, eligible professionals
within an ACO that satisfactorily report
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the measures proposed in Table 1
during the reporting period would
qualify under the Shared Savings
Program for a Physician Quality
Reporting System incentive equal to 0.5
percent of the ACO’s eligible
professionals’ total estimated Medicare
Part B PFS allowed charges for covered
professional services furnished during
the first performance period. ‘‘Covered
professional services’’ are services for
which payment is made under, or based
on, the physician fee schedule and
which are furnished under the ACO
participant’s TINs.
We plan to align the incorporated
Physician Quality Reporting System
requirements with the general Shared
Savings Program reporting
requirements, such that no extra
reporting is actually required in order
for eligible professionals or the ACO to
earn the Physician Quality Reporting
System incentive under the Shared
Savings Program. Thus, for ACOs that
meet the quality performance standard
under the Shared Savings Program for
the first performance period, the
Physician Quality Reporting System
eligible professionals within such ACOs
will be considered eligible for the
Physician Quality Reporting System
incentive under the Shared Savings
Program for that year. This means ACOs
will need to report on all measures
proposed in Table 1 in order to receive
both the Shared Savings Program shared
savings and Physician Quality Reporting
System incentive. Failure to meet the
Shared Savings Program quality
performance standard would result in
failure to be considered eligible for
shared savings, as well as failure for the
EPs within the ACO to receive a
Physician Quality Reporting System
incentive under the Shared Savings
Program for that year. ACO participant
provider/suppliers who meet the quality
performance standard but do not
generate shareable savings would still
be eligible for PQRS incentive
payments. We intend to discuss the
policy for incorporating the Physician
Quality Reporting System incentive
under the Shared Savings Program for
subsequent years in future rulemaking.
We note that ACOs will be eligible for
the Physician Quality Reporting System
incentive under the Shared Savings
Program to the extent that they contain
eligible professionals as defined under
§ 414.90(b). As a result, not all ACOs
will necessarily be eligible for the
Physician Quality Reporting System
incentive under the Shared Savings
Program. A complete list of Physician
Quality Reporting System eligible
professionals (EP) is available at:
https://www.cms.gov/PQRI/Downloads/
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EligibleProfessionals.pdf. In addition,
similar to traditional Physician Quality
Reporting System, an EP could not
qualify for the Physician Quality
Reporting System incentive as both a
group that is part of an ACO and as an
individual. Furthermore, EPs could not
qualify for a Physician Quality
Reporting System incentive under both
the Physician Quality Reporting System
under the Shared Savings Program and
the traditional Physician Quality
Reporting System. For purposes of
analysis and payment, we intend to use
TINs and National Provider
Identification numbers similar to what
we have done in the traditional
Physician Quality Reporting System (75
FR 40169), and we will provide such
details in guidance.
At this time, we are not proposing to
incorporate such payments for the EHR
Incentive Program or Electronic
Prescribing Incentive Program under the
Shared Savings Program. Professionals
in ACOs may still separately participate
in those other incentive programs.
However, we propose to require in the
Shared Savings Program measures also
included in the EHR Incentive Program
and metrics related to successful
participation in the Medicare and
Medicaid EHR Incentive Programs for
eligible professionals and hospitals and
the eRx Incentive Program, as illustrated
in Table 1. Metrics related to successful
participation in the EHR Incentive
Program and the eRx Incentive Program
includes scoring the percentage of
‘‘meaningful users’’ of certified EHR
technology, as defined in our
regulations, and the percentage of those
professionals that meet the criteria for
the eRx incentive, as measures that are
part of the quality performance
standard. These measures would be
subject to the same points scale and 30
percent or 30th percentile minimum
attainment level previously described in
table D3. We note that including metrics
based on EHR Incentive Program and
eRx Incentive Program data does not in
any way duplicate or replace specific
program measures within each of the
two respective programs or allow
eligible professionals to satisfy the
requirements of either of the two
programs through the Shared Savings
Program. To receive incentive payments
under the EHR incentive or eRx
programs (or to avoid payment
adjustments), eligible professionals will
be required to meet all the requirements
of the respective EHR and eRx
programs. In addition, as a Shared
Savings Program requirement separate
from the quality measures reporting
discussed previously, we propose
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requiring that at least 50 percent of an
ACO’s primary care physicians are
determined to be ‘‘meaningful EHR
users’’ as that term is defined in 42 CFR
495.4 as defined in the HITECH Act and
subsequent Medicare regulations by the
start of the second performance year in
order to continue participation in the
Shared Savings Program. The EHR
Incentive regulations, including the
definition of meaningful EHR user and
certified EHR technology can be found
at 42 CFR part 495, as published on July
28, 2010 (75 FR 44314). The preamble
to the July 28, 2010 final rule also
describes the stages of meaningful use.
We believe these approaches would
foster incentives for improving and
delivering high quality care by engaging
providers in performance based quality
incentive programs; and encourage
adoption of EHRs. The requirement that
at least 50 percent of ACO primary care
physicians be meaningful users
represents a first step towards achieving
our objective of incenting full
participation of ACOs’ providers in the
EHR Incentive Program over time. For
subsequent years, we anticipate
proposing greater alignment between
the Shared Savings Program and the
EHR Incentive program through future
rulemaking. We considered several
other options for incorporating other
program reporting requirements into the
Shared Savings Program. One option
was to incorporate Physician Quality
Reporting System into the Shared
Savings Program via a scaled approach,
in which how the ACO performs on the
quality measures under the Shared
Savings Program would determine the
amount of Physician Quality Reporting
System incentive an ACO could earn.
However, we thought this approach
would be burdensome and confusing to
providers who are used to a different
approach under the traditional
Physician Quality Reporting System. We
also considered proposing to limit
incorporation of the Physician Quality
Reporting System incentive under the
Shared Savings Program to the ACO’s
group practices that were used for
beneficiary assignment rather than to all
group practices associated with an ACO.
However, we thought expanding the
Physician Quality Reporting System
incentive under the Shared Savings
Program to all participant TINs within
an ACO would be more efficient for EPs
participating in both traditional
Physician Quality Reporting System and
the Physician Quality Reporting System
and the Physician Quality Reporting
System incentive under the Shared
Savings Program. This way ACOs would
report one way for the Physician Quality
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Reporting System for all of its ACO
providers/suppliers who are eligible
professionals; that is, for purposes of
qualifying for the Physician Quality
Reporting System incentive, the ACO
would not need to report one way for
the TINs used for beneficiary
assignment and another way for the
TINs not used for assignment. Another
option we considered was to
incorporate the eRx Incentive Program’s
incentive requirements and payments
into the Shared Savings Program.
However, we are not proposing to
incorporate the eRx incentive
requirements and payments under the
Shared Savings Program since the eRx
incentive ends after 2013. We believe it
would be burdensome to require ACOs
to incorporate the eRx incentive
requirements for only a 2-year period.
In concert with the proposal for 50
percent of primary care physicians to be
meaningful EHR users by the second
performance year, we seek comment on
whether we should also specify a
percentage-based requirement for
hospitals. Such a requirement would be
similar to the previous proposal for
primary care physicians and would
require 50 percent of eligible hospitals
that are ACO providers/suppliers
achieve meaningful use of certified EHR
technology by the start of the second
performance year in order for the ACO
to continue participation in the Shared
Savings Program. We also request public
comment related to circumstances
where the ACO may only include one
eligible hospital or no hospital and
whether we would need to provide an
exclusion or exemption in such a
circumstance.
We also considered limiting the
metrics related to percentage of
meaningful users to be applicable to the
Medicare EHR Incentive Program only,
since presumably ACO providers/
suppliers may see a high proportion of
Medicare FFS patients. However, we
realize that ACO providers/suppliers
eligible for the EHR incentive may seek
to qualify for the EHR incentive through
any of the EHR Incentive Programs
available to Medicare and Medicaid
eligible professionals and hospitals.
Finally, we considered incorporating
EHR Incentive Program’s incentive
requirements into the Shared Savings
Program, however, per the previous
discussion, we did not believe the
program was ready for incorporation at
this time. Furthermore, we are
proposing that ACOs report quality
measures as a group, and the EHR
Incentive program does not include a
group reporting option at this time.
We invite comment on our proposal
to incorporate Physician Quality
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Reporting System requirements and
payments and certain metrics related to
under the Shared Savings Program, as
well as the options discussed previously
that we considered.
6. Public Reporting
Increasingly, transparency of
information in the health care sector is
seen as a means to facilitate more
informed patient choice, offer
incentives, and feedback that help
improve the quality and lower the cost
of care, and improve oversight with
respect to program integrity. Examples
of existing efforts that improve
transparency include Hospital Compare,
which enables patients along with their
family and health care providers to
compare the quality of care provided in
the hospitals that agree to submit data
on the quality of certain services they
provide for certain conditions. Hospital
Compare displays the following kinds of
information:
• Rates for process of care measures
that show whether or not hospitals
provide some of the care that is
recommended for patients being treated
for a heart attack, heart failure,
pneumonia, asthma (children only) or
patients having surgery.
• Information on hospital outcome of
care measures, including 30-day risk
adjusted death (mortality) and
readmission rates.
• Data collected from the Hospital
Consumer Assessment of Healthcare
Providers and Systems (HCAHPS)
Survey, reflecting patients’ hospital
experiences.
• Medicare inpatient hospital
payment information.
• The number of Medicare patients
treated for certain illnesses or diagnoses
(as reported by Medicare severitydiagnosis related groups (MS–DRGs)).
(For more information, see the
Hospital Compare Web site at https://
www.hospitalcompare.hhs.gov/hospitalsearch.aspx?
AspxAutoDetectCookieSupport=1.)
Similarly, Nursing Home Compare
reports detailed information about every
Medicare and Medicaid-certified
nursing home in the country. Nursing
Home Compare includes comparative
information on health inspection results
such as: (1) An assessment of the care
of residents; (2) the process of care; (3)
staff and resident interactions; and (4)
the nursing home environment; (5)
nursing home staffing; and quality
measures. (For more information, see
the Nursing Home Compare Web site at
https://www.medicare.gov/NHCompare/
Include/DataSection/Questions/
SearchCriteriaNEW.asp?version=
default&browser=
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IE%7C6%7CWinXP&language=
English&defaultstatus=
0&pagelist=Home&Cookies
EnabledStatus=True.)
The Affordable Care Act included
several new initiatives that will expand
transparency in the Medicare program.
Among these, section 3003 of the
Affordable Care Act will make aggregate
information on physician resource use
publicly available; section 3004 of the
Affordable Care Act will make quality
data relating to long-term care hospitals,
inpatient rehabilitation facilities, and
hospices publicly available; and section
3005 of the Affordable Care Act will
make quality data for certain cancer
hospitals publicly available. Similarly,
section 10331 of the Affordable Care Act
requires the Secretary to develop a
Physician Compare Internet Web site by
January 1, 2011 with information on
physicians enrolled in the Medicare
program and other eligible professionals
who participate in the Physician Quality
Reporting Initiative. Not later than
January 1, 2013, the Secretary must also
implement a plan for making
information on quality and patient
experience measures publicly available.
Further, in developing this plan and as
determined appropriate, the Secretary
must consider the plan to transition to
a value-based purchasing program for
physicians and other practitioners
developed under section 131 of the
Medicare Improvements for Patients and
Providers Act of 2008 (Pub. L. 110–275).
Section 10332 of the Affordable Care
Act requires the Secretary to make
certain standardized claims data under
Medicare Parts A, B, and D available to
entities qualified by the Secretary to use
these data to evaluate the performance
of providers of services and suppliers on
measures of quality, efficiency,
effectiveness, and resource use.
While the Act did not include a
specific requirement for public
reporting and transparency related to
the Shared Savings Program, improved
transparency would support a number
of program requirements. In particular,
increased transparency would be
consistent with and support the
requirement under section 1899(b)(2)(A)
of the Act for ACOs to be willing to
‘‘become accountable for the quality,
cost, and overall care’’ of the Medicare
beneficiaries assigned to it.
Public reporting of ACO cost and
quality measure data would improve a
beneficiary’s ability to make informed
health care choices, and facilitate an
ACO’s ability to improve the quality and
efficiency of its care by making available
information that enables ACO
professionals to assess their
performance relative to their peers, and
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creates incentives for those
professionals to improve their
performance. For example, the
transparency of outcomes that results
when consumers have access to publicly
reported performance information could
be an important catalyst for providers to
continually seek to improve their
performance. Further, many other
stakeholders, including health plans,
employers, and policy makers have an
interest in knowing the degree to which
different health care delivery models are
effective in improving quality and
reducing costs. Timely dissemination of
reports on ACO quality and cost
performance will contribute to the
dialogue, at the national, regional and
local level, on how to drive
improvement and innovation in health
care.
Therefore, we believe it is desirable
and consistent with section
1899(b)(2)(A) of the Act for several
aspects of an ACO’s operation and
performance to be transparent to the
public—specifically, information
regarding: (1) Providers and suppliers
participating in the ACO; (2) parties
sharing in the governance of the ACO;
(3) quality performance standard scores;
and (4) general information on how an
ACO shares savings with its members.
We are proposing that certain
information regarding the operations of
the ACO would be subject to public
reporting to the extent administratively
feasible and permitted by law.
Specifically, we propose that the
following information regarding the
ACO be publicly reported:
• Name and location.
• Primary contact.
• Organizational information
including—
++ ACO participants;
++ Identification of ACO participants
in joint ventures between ACO
professionals and hospitals;
++ Identification of the ACO
participant representatives on its
governing body; and
++ Associated committees and
committee leadership.
• Shared savings information
including—
++ Shared savings performance
payment received by ACOs or shared
losses payable to us; and
++ Total proportion of shared savings
invested in infrastructure, redesigned
care processes and other resources
required to support the three-part aim
goals of better health for populations,
better care for individuals and lower
growth in expenditures, including the
proportion distributed among ACO
participants.
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• Quality performance standard
scores.
In the interest of transparency, it is
important that the ACO make available
to the public information on its
accountability for the quality, cost, and
the overall care furnished to its assigned
beneficiary population. We are
proposing that each ACO be responsible
for making this information available to
the public in a standardized format that
we will make available through
subregulatory guidance. This
requirement would be included in each
ACO’s 3-year agreement.
We seek comments on our proposals,
including whether the proposed list
includes elements that should not be
required, or excludes elements that are
important for achieving transparency or
meaningful public disclosure within the
Shared Savings Program and whether
we should standardize the format or
allow ACOs the flexibility to try
different and innovative approaches for
providing this information to
beneficiaries. We welcome comment on
these requirements and new reporting
requirement recommendations that
could be considered for future program
years through future rulemaking. Also,
we seek comment on whether ACOs
themselves should be required to make
this information publicly available or
whether ACOs should report this
information to us, and we would then
make this information publicly
available.
7. Aligning ACO Quality Measures With
Other Laws and Regulations
The standards for Accountable Care
Organizations proposed in this rule are
among the first quality standards for
doctors and health care organizations
established under the Affordable Care
Act. As such, we believe that they
represent an opportunity to continue a
robust discussion between the Federal
government, affected parties such as
physicians, hospitals, and patients, and
all other stakeholders on developing
and aligning the best possible
framework for ensuring quality care.
The Act directs the Department to
promulgate quality standards and
require accountability or reporting in
several sections. It calls for a National
Quality Strategy that was released on
March 21, 2011. We have already
proposed standards for inpatient
hospitals and the Medicaid program
through rulemaking, as well as the
standards for ACOs outlined in this
rule. These standards affect different
constituencies, including physicians,
hospitals, other providers, and patients
and their families. As such, we have
proposed distinct domains and
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Care Act program as illustrated in Table
5.
While these quality domains and
categories—and the parties that they
affect—overlap in a number of areas,
each set of standards has different
domains, categories, and specific
measures. We recognize that different
quality frameworks and rewards may
add to confusion and administrative
burdens for affected parties, and
mitigate efforts to focus on the highestquality care. We seek comment from
affected parties and other stakeholders
on the best and most appropriate way to
align quality domains, categories,
specific measures, and rewards across
these and other Federal healthcare
programs, to ensure the highest-possible
quality of care. Specifically, we seek
comment on whether quality standards
in different Affordable Care Act
programs should use the same
definition of domains, categories,
specific measures, and rewards for
performance across all programs to the
greatest extent possible, taking into
account meaningful differences in
affected parties.
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F. Shared Savings Determination
1. Background
Section 1899 of the Act, as added by
section 3022 of the Affordable Care Act,
establishes the general requirements for
payments to participating ACOs.
Specifically, section 1899(d)(1)(A) of the
Act provides that ACO participants will
continue to receive payment ‘‘under the
original Medicare fee-for-service
program under Parts A and B in the
same manner as they would otherwise
be made.’’ However, section
1899(d)(1)(A) of the Act also provides
for ACOs to receive payment for shared
Medicare savings provided that the ACO
meets both the quality performance
standards established by the Secretary,
as discussed in section II.E. of proposed
rule, and demonstrates that it has
achieved savings against a benchmark of
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expected average per capita Medicare
FFS expenditures. Additionally, section
1899(i) of the Act authorizes the
Secretary to use other payment models
in the place of the one-sided model
outlined in section 1899(d) of the Act.
This provision authorizes the Secretary
to select a partial capitation model or
any other payment model that the
Secretary determines will improve the
quality and efficiency of items and
services furnished to Medicare
beneficiaries without additional
program expenditures.
In the November 17, 2010 Federal
Register, we solicited public comment
on a number of issues regarding ACOs
and the Shared Savings Program,
including the types of additional
payment models we should consider in
addition to the model laid out in section
1899(d) of the Act, either under the
authority provided in 1899(i) of the Act
or using the Innovation Center authority
under section 1115A of the Act. We
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different frameworks for rewarding
performance, under each Affordable
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further asked about the relative
advantages and disadvantages of any
such payment models.
We considered several options for
structuring the Shared Savings Program.
One option we considered was to offer
a pure one-sided shared savings
approach using the calculation and
payment methodology under 1899(d) of
the Act. This option would have the
potential to attract a large number of
participants to the program and
introduce value-based purchasing
broadly to providers and suppliers,
many of whom may never have
participated in a value-based purchasing
initiative. Another reason we
considered this option was that a onesided model with no downside risk
might be more accessible and attract
smaller group participation. However,
as some commenters suggest, while
such a model may provide incentive for
participants to improve quality, it may
not be enough of an incentive for
participants to improve the efficiency of
health care delivery and cost. Therefore,
we considered whether we should
instead focus on our authority under
section 1899(i) of the Act to create a
risk-based option in the Shared Savings
Program. Such a model would have the
advantage of providing an opportunity
for more experienced ACOs that are
ready to share in losses to enter a
sharing arrangement that provides
greater reward for greater responsibility.
Another option would be to offer a
hybrid approach. A hybrid approach
would combine many of the elements of
the one-sided model under section
1899(d) of the Act with a risk-based
approach under section 1899(i) of the
Act. The hybrid approach would have
the advantage of providing an entry
point for organizations with less
experience with risk models, such as
some physician-driven organizations or
smaller ACOs, to gain experience with
population management before
transitioning to a risk-based model
while also providing an opportunity for
more experienced ACOs that are ready
to share in losses to enter a sharing
arrangement that provides greater
reward for greater responsibility.
Based on the input of commenters on
the November 17, 2010 RFI, other
stakeholders and policy experts we are
proposing to implement a hybrid
approach. Specifically, we are
proposing that ACOs participating in
the Shared Savings Program will have
an option between two tracks:
Track 1: Under Track 1, shared
savings would be reconciled annually
for the first 2 years of the 3-year
agreement using a one-sided shared
savings approach, with ACOs not being
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responsible for any portion of the losses
above the expenditure target. However,
for the third year of the 3-year
agreement, we will use our authority
under section 1899(i) of the Act to
establish an alternative two-sided
payment model. Under this model, an
ACO would be required to agree to share
any losses that may be generated as well
as savings. The portion of shared losses
that the ACO would be at risk for in the
third year of the agreement is further
described in section II.G. of this
proposed rule. ACOs that enter the
Shared Savings Program under Track 1
would be automatically transitioned to
the two-sided model in the third year of
their agreement period. In that year, the
ACO’s payments would be reconciled as
if it was in the first year of the two-sided
model. However quality scoring would
still be based on the methods for the
third year (that is, it would not revert
back to the first year standard of full and
accurate reporting). Thereafter, those
ACOs that wish to continue
participating in the Shared Savings
Program would only have the option of
participating in Track 2, that is, under
the two-sided model.
Track 2: More experienced ACOs that
are ready to share in losses with greater
opportunity for reward may elect to
immediately enter the two-sided model
(as discussed in section II.G. of this
proposed rule). An ACO participating in
Track 2 would be under the two-sided
model for all three years of its
agreement period. Under this model, the
ACO would be eligible for higher
sharing rates than would be available
under the one-sided model.
Unless specifically noted, the
elements discussed in the rest of this
section will apply to both the one-sided
and two-sided models. Section II.G. of
this proposed rule provides additional
detail regarding aspects of the two-sided
model that are not discussed in this
section.
We seek comment on our proposal
and the alternatives discussed
previously.
2. Overview of Shared Savings
Determination
The basic requirements for
establishing and updating the
benchmark, as well as determining
whether an ACO has achieved savings
against the benchmark, are outlined in
section 1899(d)(1)(B) of the Act. Section
1899(d)(1)(B)(i) of the Act establishes
that an ACO shall be eligible for
payment of shared savings ‘‘only if the
estimated average per capita Medicare
expenditures under the ACO for
Medicare FFS beneficiaries for Parts A
and B services, adjusted for beneficiary
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19603
characteristics, is at least the percent
specified by the Secretary below the
applicable benchmark * * * .’’ We will
take into account payments made from
the Medicare Trust Fund for Parts A and
B services, for assigned Medicare FFS
beneficiaries, including payments made
under a demonstration, pilot or time
limited program when computing
average per capita Medicare
expenditures under the ACO. The
statute further requires the Secretary to
establish the percentage that
expenditures must be below the
applicable benchmark ‘‘to account for
normal variation in expenditures under
this title, based upon the number of
Medicare fee-for-service beneficiaries
assigned to an ACO.’’ We will refer to
this percentage as the ‘‘minimum
savings rate’’ (MSR).
Section 1899(d)(1)(B)(ii) of the Act
requires the Secretary to establish and
update the ‘‘benchmark for each
agreement period using the most recent
available 3 years of per-beneficiary
expenditures for parts A and B services
for Medicare fee-for-service
beneficiaries assigned to the ACO.’’ This
section also requires the benchmark to
‘‘be adjusted for beneficiary
characteristics and such other factors as
the Secretary determines appropriate
and updated by the projected absolute
amount of growth in national per capita
expenditures for Parts A and B services
under the original Medicare fee-forservice service program, as estimated by
the Secretary.’’ A new benchmark is to
be established consistent with these
requirements at the beginning of each
new agreement period.
Section 1899(d)(2) of the Act provides
that, if the ACO meets the quality
performance standards established by
the Secretary, as discussed in section
II.E. of this proposed rule ‘‘a percent
(as determined appropriate by the
Secretary) of the difference between
such estimated average per capita
Medicare expenditures in a year,
adjusted for beneficiary characteristics,
under the ACO and such benchmark for
the ACO may be paid to the ACO as
shared savings and the remainder of
such difference shall be retained by the
program under this title.’’ We will refer
to this percentage as the ‘‘sharing rate.’’
This section also requires the Secretary
to ‘‘establish limits on the total amount
of shared savings that may be paid to an
ACO.’’ We will refer to this limit as the
‘‘sharing cap’’.
Thus, in order to implement the
provisions of section 1899(d) of the Act
for determining and appropriately
sharing savings, we must make a
number of determinations about the
specific design of the shared savings
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methodology described by the statute.
First, we must establish an expenditure
benchmark, which involves
determining: (1) The patient population
(that is, assigning patients to ACOs for
purposes of quality and financial
performance measurement) for whom
the benchmark is calculated; (2)
appropriate adjustments for beneficiary
characteristics such as demographic
factors and/or health status that should
be taken into account in the benchmark;
(3) whether any other adjustments to the
3-year benchmark are warranted, such
as to avoid potentially disadvantaging
various types of providers (for example,
hospitals that receive Medicare
disproportionate share hospital
payments (DSH hospitals) or teaching
hospitals that receive indirect graduate
medical education (IME) payments) or
ACOs located in high cost, or low cost,
areas; and (4) appropriate methods for
trending the 3-year benchmark forward
to the start of the agreement period, and
subsequently for updating the
benchmark for each of the 3
performance years of the agreement
period with the ACO.
Second, we must compare the
benchmark to the assigned beneficiary
per capita Medicare expenditures in
each performance year under the
agreement period in order to determine
the amount of any savings.
Third, we must establish the
appropriate MSR, as required by the
statute ‘‘to account for normal variation
in expenditures * * * based upon the
number of Medicare fee-for-service
beneficiaries assigned to an ACO’’ and
we must determine the appropriate
sharing rate for ACOs that have realized
savings against the benchmark above the
MSR. Finally, we must determine the
required sharing cap on the total
amount of shared savings that may be
paid to an ACO. We discuss all these
issues, and our proposals for addressing
them, in this section.
3. Establishing an Expenditure
Benchmark
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a. Background
Section 1899(d)(1)(B)(ii) of the Act
specifies several requirements with
regard to establishing an ACO’s
benchmark.
• First, the law requires the Secretary
‘‘to estimate a benchmark for each
agreement period for each ACO using
the most recent available 3 years of perbeneficiary expenditures for parts A and
B services for Medicare fee-for-service
beneficiaries assigned to the ACO.’’
• Second, the law requires that
‘‘[s]uch benchmark shall be adjusted for
beneficiary characteristics and such
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other factors as the Secretary determines
appropriate.’’
• Third, the law requires that the
benchmark be ‘‘updated by the projected
absolute amount of growth in national
per capita expenditures for parts A and
B services under the original Medicare
fee-for-service program, as estimated by
the Secretary.’’
• Finally, the law requires that
‘‘[s]uch benchmark shall be reset at the
start of each agreement period.’’
A useful way to view the benchmark
is as a surrogate measure of what the
Medicare FFS Parts A and B
expenditures would otherwise have
been in the absence of the ACO. Once
the savings realized by the ACO exceed
a margin for normal variation in
expenditures from year-to-year (what we
call the MSR described in more detail
later in this proposed rule), the
difference between actual expenditures
of the ACO’s assigned beneficiaries
during each year of the agreement
period and its benchmark (updated,
according to statute as described in
more detail later in the document)
should reflect how well the ACO is
coordinating care for these beneficiaries
and improving the overall efficiency of
their care.
An accurate benchmark estimate is
important in order to ensure that an
ACO that successfully coordinates care
and achieves real savings is rewarded
with shared savings. Similarly, an
accurate benchmark estimate helps to
ensure that shared savings are not
inadvertently paid to an ACO that does
not successfully coordinate care well or
that has not achieved savings in excess
of normal variation in annual
expenditures.
We have considered two legally
permissible approaches to meeting the
statutory language for estimating the
benchmark, which we will call Option
1 and Option 2 in this proposed rule.
Both approaches involve benchmarks
that are derived from prior expenditures
of assigned beneficiaries and adjusted
for certain beneficiary characteristics,
and other factors, the Secretary
determines appropriate and updated by
the projected absolute amount of growth
in national per capita expenditures.
Under both approaches, the benchmark
would also be reset at the start of each
agreement period. However, a key
difference between these two
approaches is the beneficiary
population used to determine
expenditures for purposes of the
benchmark. Specifically, under Option
1, we would estimate an ACO’s
benchmark based on the Parts A and B
FFS expenditures of beneficiaries who
would have been assigned to the ACO
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in each of the 3 years prior to the start
of an ACO’s agreement period using the
ACO participants’ TINs. In contrast,
under Option 2, the benchmark would
be based on the Parts A and B FFS
expenditures of beneficiaries, who are
actually assigned to the ACO during
each performance year, with the
expenditures being those incurred in the
3 years immediately preceding the
ACO’s agreement period for those
assigned beneficiaries. We describe
these two options later in this
document. In this proposed rule, we are
proposing Option 1 to establish each
ACO’s benchmark; however, we solicit
comments on both options.
b. Option 1
Under Option 1, we would estimate
the benchmark for an ACO for an
agreement period starting with the TINs
of ACO participants identified at the
start of the agreement period. The same
rules that will be used to determine
assignment of beneficiaries to ACOs
during the agreement period would be
applied to these data. Accordingly,
consistent with the assignment
methodology proposed in section II.D.
of this proposed rule, we would use the
claim records of these ACO participants
to determine a list of beneficiaries who
received a plurality of their primary care
services from primary care physicians
participating in the ACO in each of the
prior 3 most recent available years.
Using the per capita Parts A and B
FFS expenditures for beneficiaries that
would have been assigned to the ACO
in each of these 3 prior years, we will
estimate a fixed benchmark that is
adjusted for overall growth and
beneficiary characteristics, including
health status using prospective HCC
adjustments (as discussed in section 3
later in this document). This benchmark
would then be updated annually during
the agreement period, according to
statute, based on the absolute amount of
growth in national per capita
expenditures for Parts A and B services
under the original Medicare FFS
program.
• The first step in this process is to
calculate annual Parts A and B FFS per
capita expenditures for the beneficiaries
who would have been assigned for each
of the benchmark years. To minimize
variation from catastrophically large
claims, we would truncate an assigned
beneficiary’s total annual Parts A and B
FFS per capita expenditures at the 99th
percentile as determined for each
benchmark year (for example roughly
$100,000 in 2008). We would also
truncate an assigned beneficiary’s total
annual Parts A and B FFS per capita
expenditures at the 99th percentile as
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determined for each subsequent
performance year.
• Next, using our Office of the
Actuary national Medicare expenditure
data for each of the years making up the
benchmark, we would determine an
appropriate growth index and trend
them to benchmark year 3 (BY3) dollars.
Our proposed method for trending
expenditures is discussed in section
II.F.7.of this proposed rule.
• Using health status measures for the
beneficiary population in each of the
years making up the benchmark, we
would establish health status indices for
each year and adjust so they are restated
to reflect BY3 risk. Our approach to
account for health status is discussed
section II.F.3. of this proposed rule.
• Next, we would compute a 3-year
risk-and growth-trend adjusted per
capita expenditure amount for the
patient populations in each of the 3
benchmark years by combining the
initial per capita expenditures for each
year with the respective growth and
health status indices. This yields risk
adjusted per capita expenditures for
beneficiaries historically assigned to the
ACO in each of the 3 years used to
establish the benchmark stated in BY3
risk and expenditure amounts.
• We propose to weight the most
recent year of the benchmark, BY3 at 60
percent, BY2 at 30 percent and BY1 at
10 percent so that we can ensure the
benchmark reflects more accurately the
latest expenditure and health status of
the ACO’s assigned beneficiary
population. This weighting allows us to
establish lower MSRs since the
weighting results in a more accurate
benchmark.
• Last, as required by statute, for each
performance year we would update this
fixed benchmark by the projected
absolute amount of growth in national
per capita expenditures for Parts A and
B services under the original Medicare
FFS program using data from our Office
of the Actuary. This approach for
updating the benchmark avoids current
law issues associated with Medicare
expenditure projections since it uses the
actual claims and expenditure
experience for Medicare patients to
calculate the factor used to update the
benchmark for purposes of annual
reconciliation. Consistent with the
statutory requirement, the benchmark
and its associated computations would
only be rebased at the start of a new
agreement period.
As described in section II.C. of this
proposed rule, if requested by the ACO,
we are proposing to provide the ACO
with aggregated data and information on
beneficiaries that would historically
have been assigned to the ACO and, as
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a result, have a likelihood of being
assigned during the agreement period.
It is possible that to the extent that an
ACO’s population or its composition of
ACO providers/suppliers change over
time, the assigned population could
diverge from the benchmark population,
potentially affecting the comparability
of performance measurement. Modeling
the PGP demonstration data using the
proposed primary care based
assignment methodology revealed that
assignment of beneficiaries varies from
year-to-year, with about 25 percent of
those assigned in one year not being
assigned in the subsequent year (due to
relocation, death, participation in MA,
or changes in their choice of care
professionals). This was consistent
across organizations participating in the
demonstration which were also
geographically diverse. We believe the
approach to establishing the benchmark
described previously would provide a
relatively accurate reflection of the
average population of Medicare FFS
beneficiaries that receive their care from
the ACO participants during the ACO
agreement period. However, because the
FFS population served by the ACO
changes from year to year, some of the
beneficiaries whose expenditures would
be included in the benchmark with this
approach would not be reflected in the
population assigned to the ACO during
the years of the ACO agreement period.
It is also possible that this benchmark
approach could provide unwanted
incentives to seek and/or avoid specific
beneficiaries during the agreement
period so that average expenditures
would more likely be less than for their
historical beneficiaries included in the
benchmark. Therefore we also
considered a second option that relies
on developing a benchmark based on
the populations of specific beneficiaries
who are actually assigned to the ACO
during the agreement period.
c. Option 2
Under this option, for each
beneficiary assigned to the ACO during
the agreement period, we would
calculate their per capita Parts A and B
FFS expenditures during each of the 3
years immediately preceding the first
year of the agreement period. These
amounts would be trended to the start
of the agreement period as was
described for Option 1, that is, since
Option 2 also requires risk adjustment,
we will adjust the benchmark for health
status using the same prospective CMS–
Hierarchal Condition Category (CMS–
HCC) risk adjuster and apply it to
calculate the benchmark in the same
manner as described for Option 1.
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To meet the statutory requirement to
adjust the benchmark for ‘‘beneficiary
characteristics’’ we would adjust the
annual per capita expenditures to
account for changes in health status.
For beneficiaries without 3 full years
of immediately-prior Medicare
eligibility (such as beneficiaries who
were not 68 in their first year assigned
to the ACO), a further adjustment would
be necessary under this option.
• For those beneficiaries with less
than one full year of prior Medicare
experience, we would either—
++ Use a substitute for their own
expenditures in the update amount
within the benchmark, that is, substitute
the average per capita FFS expenditures
for all Medicare beneficiaries during the
year they are first assigned to the ACO,
adjusted for health status (as described
later in the document in section 3); or
++ Exclude their experience from the
shared savings computations.
• For those assigned beneficiaries
with more than 12 months prior
Medicare experience but less than 36
months we also have two choices:
++ Compute a weighted-average
(using number of months as the weight)
that blends.
—Their prior expenditure experience
and
—The average per capita Parts A and B
FFS expenditures for all Medicare
beneficiaries during the year before
the first year they are assigned to the
ACO, adjusted for health status; or
++ Use only their prior expenditure
experience.
We seek comments about these
adjustment approaches and solicit other
approaches we might consider.
After the benchmark is adjusted for
beneficiary health status, the benchmark
would also be updated by the applicable
projected amount of growth in national
per capita expenditures for Parts A and
B services under the original Medicare
FFS program as was described for
Option 1.
For the second and third year of the
agreement period, we would make no
further adjustments for assigned
beneficiaries who were also assigned in
the first year of the ACO agreement
period. However, in the second and
third year of the agreement, there will
also be newly-assigned beneficiaries as
well as previously-assigned
beneficiaries who are no longer assigned
to the ACO. The benchmark would be
adjusted to account for these changes.
We would adjust the benchmark by
adding the experience of the newlyassigned beneficiaries (as discussed
previously for the first year) for the 3
years prior to the agreement period, and
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by removing the prior experience of the
no-longer assigned beneficiaries. In the
case of a beneficiary who was assigned
during the first year, not assigned
during the second year, and then again
assigned during the third year of the
ACO’s agreement period, the prior
expenditure experience that would be
used to adjust the benchmark in the
third year would be the same amount
initially used for their first year of
assignment. These adjustments would
yield a benchmark for each ACO that is
estimated using beneficiary
expenditures for the three years prior to
the agreement period for only those
beneficiaries that were actually assigned
to the ACO during that year of the
agreement period.
Additionally, Option 2 would require
an adjustment for assigned beneficiaries
who die during an agreement year. We
know that approximately 5 percent of
all Medicare beneficiaries die in a single
year, and that their average monthly
expenditures are often higher during
this last year of life compared to the
immediately preceding years. For these
beneficiaries, the benchmark might
therefore not be a fair basis for
comparison with actual expenditures for
purposes of determining shared savings,
which could create incentives for ACOs
to avoid assignment of beneficiaries
who may be in their last year of life or
treat such beneficiaries differently. This
would not be the case for Option 1 as
that benchmark approach would
include the average per capita costs of
beneficiaries who died during the
benchmark period. We are therefore
considering one of two methods to
adjust for this beneficiary characteristic
within Option 2.
Under the first method for adjusting
for decedents, we would propose to
exclude the expenditures of deceased
beneficiaries from actual expenditures
during the agreement period. We believe
this approach would best avoid
concerns about creating incentives for
ACOs to avoid assignment of
beneficiaries in their last year of life or
treat such beneficiaries differently. In a
second method for adjusting for
decedents, we would compare average
expenditures for each deceased
beneficiary during the agreement year to
the average expenditures for
beneficiaries included in the
benchmark.
• If the agreement year’s expenditures
were 5 percent or less above the
benchmark, we would make no
adjustment;
• If the agreement year’s expenditures
were greater than 5 percent above the
benchmark, we would need to decide
upon an acceptable method to adjust the
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accumulated expenditures for deceased
beneficiaries.
Of these two methods for adjusting for
decedents during the course of the
performance year under Option 2, our
preference is for the first method.
However, we invite comments on both
of these methods, and any others that
might be suggested for adjusting for
decedents during the course of the
performance year under Option 2.
The second method is intended to
address the implications of changes to
an ACO’s population over time, but this
option would require additional data
adjustments and computations that are
not required under the first method.
However, to the extent that average
per capita expenditures for all
beneficiaries differs from the average for
the geographic area in which an ACO
operates, the first method previously
discussed would effectively be imputing
a value that is likely to be somewhat
higher or lower than would actually be
expected for that ACO. Alternatively,
excluding the experience of
beneficiaries with less than 1 full year
of experience from the shared savings
computations as contemplated in the
second method previously discussed,
would reduce the size of an ACO’s
beneficiary population, increasing the
MSR that would be needed before an
ACO would be eligible to share savings.
This could have the effect of
discouraging participation among
smaller ACOs, for example, in rural
areas. Likewise, we would expect a
similar impact on an ACO’s MSR if
deceased beneficiaries were excluded
from the shared savings computations as
is previously proposed.
d. Summary
We believe both Option 1 and Option
2 are legally permissible approaches to
setting the expenditure benchmark,
adjusting for beneficiary characteristics,
and updating by the projected absolute
amount of growth in national per capita
expenditures. We also believe that both
approaches can establish viable
benchmarks to measure ACO
performance over time and provide
incentives for ACOs to improve their
processes and outcomes during the
agreement period.
We are proposing to adopt Option 1
for establishing ACO benchmarks, but
seek comments on the merits and
limitations of both options, particularly
with respect to how each approach
might affect the willingness of ACOs or
particular types of ACO to participate in
the Shared Savings Program, create
incentives for ACOs to seek or avoid
certain kinds of beneficiaries, and
impact Medicare expenditures.
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Moreover, we will continue to examine
the merits and potential effects of both
options over the next several months. If,
based on our findings and the comments
received in response to this proposal,
we determine that Option 2 would be a
more appropriate method for
establishing a benchmark, we would
expect to adopt that option in the final
rule.
4. Adjusting the Benchmark and
Average per Capita Expenditures for
Beneficiary Characteristics
Section 1899(d)(1)(B)(i) of the Act
stipulates that an ACO is eligible for
shared savings ‘‘only if the estimated
average per capita Medicare
expenditures under the ACO for
Medicare fee-for-service beneficiaries
for Parts A and B services, adjusted for
beneficiary characteristics’’ is below the
applicable benchmark. Likewise, section
1899(d)(1)(B)(ii) of the Act specifies that
the benchmark ‘‘shall be adjusted for
beneficiary characteristics and such
other factors as the Secretary determines
appropriate * * *.’’ This requirement to
adjust for ‘‘beneficiary characteristics’’
implicitly recognizes that, under a
shared savings model, the realization of
savings against a benchmark could be a
function of two factors. One factor is
reduced expenditure growth as a result
of greater quality and efficiency in the
delivery of health care services. The
other factor could be changes in the
characteristics of the beneficiaries who
are under the care of the ACO. Thus, in
the absence of risk adjustment, some
organizations may realize savings
merely because of treating a patient mix
with better health status than the patient
population reflected in the benchmark.
On the other hand, some organizations
may share in savings on a risk adjusted
basis but would not have shared in
savings if expenditures were not risk
adjusted.
Beneficiary health status can be
measured using various tools, under
which beneficiaries are typically
assigned ‘‘risk scores’’ that reflect their
demographic and diagnostic conditions
and offer an estimate of the relative
extent to which they are likely to utilize
medical services compared to other
beneficiaries. Performance payments are
a function of the ACO’s success in
controlling expenditure growth and
changes in the health status of the
assigned population, thus they are
sensitive to changes in risk scores.
However, an ACO’s ability to share in
savings can be affected not only by
changes in the health status of a
population but also by changes in
coding intensity and changes in the mix
of specialists and other providers within
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an ACO, which in turn could affect the
characteristics of its assigned
beneficiary population, relative to the
benchmark period. Our goal is to
measure improvements in care delivery
of an ACO and to make appropriate
adjustments to reflect the health status
of assigned patients as well as changes
in the ACOs organizational structure
that would affect the case mix of
assigned patients rather than apparent
changes arising from the manner in
which ACO providers/suppliers code
diagnoses. Thus, when applying a risk
adjustment model, it is necessary to
guard against changes that result from
more specific or comprehensive coding
as opposed to improvements in the
coordination and quality of health care.
The statute clearly calls for the
characteristics of the beneficiaries
assigned to an ACO to be taken into
account in estimating both an ACO’s
benchmark and its expenditures during
the agreement period. This requirement
helps to ensure that quality and
efficiency in the delivery of health care
services are the basis for realizing and
sharing savings under the Shared
Savings Program. Because we want to
create an environment where ACOs are
encouraged to effectively coordinate
care for beneficiaries with complex
illnesses, and not create an environment
where ACOs have incentive to avoid
these types of beneficiaries, we believe
that relative health status is one such
beneficiary characteristic that should be
reflected in the calculation of average
per capita expenditures for purposes of
both the benchmark and actual
expenditures during the agreement
period. We have considered two basic
options for risk adjusting the average
per capita expenditures in order to
reflect beneficiary characteristics.
One option is to employ a method
that considers only patient demographic
factors, such as age, sex, Medicaid
status, and the basis for Medicare
entitlement (that is, age, disability or
ESRD), without incorporating diagnostic
information. The second option is to
employ a methodology that incorporates
diagnostic information, specifically the
CMS–HCC prospective risk adjustment
model that has been used under the MA
program. In addition to demographic
variables, the CMS–HCC prospective
risk adjustment model uses
beneficiaries’ prior year diagnoses to
develop risk scores that are then applied
to their current year expenditures. The
model is widely accepted by payers and
providers, and risk scores are annually
calculated for all Medicare beneficiaries
by us, so readily available data can be
incorporated into the Shared Savings
Program. Additional information on the
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CMS–HCC model can be found in the
Advance Notice of Methodological
Changes for Calendar Year (CY) 2011 for
Medicare Advantage (MA) Capitation
Rates, Part C and Part D Payment
Policies and 2011 Call Letter, which can
be found at https://www.cms.gov/
MedicareAdvtgSpecRateStats/
Downloads/Advance2011.pdf and
https://www.cms.gov/
MedicareAdvtgSpecRateStats/
Downloads/Announcement2011.pdf.
As discussed previously, a key issue
when using a risk adjustment model
that incorporates diagnosis data is that
risk scores can be affected not just by
changes in the health status of the
population but also by changes in
coding intensity and by the mix of
specialists and providers furnishing
services. The experience in MA clearly
shows that health plans can
significantly increase the HCC score of
their populations by focusing on more
complete coding. Similarly, our
experience with the PGP demonstration
shows that participating sites have an
incentive to code more fully or intensely
because of the potential impact on
performance payments, to provide more
accurate measurement and reporting of
quality measures, as well as to provide
for more complete and accurate
information that can be used for
population management.
If we adopt a risk adjustment
methodology in the Shared Savings
Program that incorporates diagnostic
data, we expect that ACOs would have
a similar incentive to code more fully
for purposes of population management,
quality reporting and to optimize their
risk scores for the purpose of achieving
shared savings. Because they are
responsible for the delivery of care, and
can control the information included in
Parts A and B claims, the ACO
providers/suppliers could potentially
increase the risk scores for their FFS
patients by more completely reporting
diagnoses. The practical effect of
increasing risk scores would be to
decrease the actual annual expenditures
compared to the benchmark, because
the benchmark would be increased to
reflect changes in the ACO’s risk score,
while actual expenditures would not
change. As a result, the ACO’s chances
of demonstrating savings and receiving
a shared savings payment would
improve. Behaviors such as these could
allow an ACO to achieve apparent
savings by coding changes alone and
without improved methods of
beneficiary care.
We have made adjustments to account
for the upward trend in risk scores in
other programs. For example, for the
MA program we make adjustments to
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account for the upward trend in FFS
diagnostic coding and CMS–HCC model
changes through normalization factors
and coding intensity adjustments.
Another approach to addressing this
upward trend in diagnostic coding
would be to incorporate an annual cap
in the amount of risk score growth we
would allow for each ACO. One option
for setting the annual cap could be
setting a fixed growth percentage for all
ACOs, and any increase in risk score
growth above the cap would be negated.
A challenge to this approach would be
determining a generally acceptable sized
cap. A second option would be to
establish a risk score for the ACO’s
assigned population during the
agreement period based on the
calculated risk score of beneficiaries
who were used to calculate the ACO’s
benchmark. This would establish an
annual cap, that is based on experience
specific to each individual ACO and
would thus result in an individually
calculated cap for each ACO. Yet
another alternative we considered for
addressing the upward trend in coding
intensity would be to use a methodology
similar to the MA methodology that
would reduce the amount of growth in
the risk scores for beneficiaries assigned
to the ACOs, but continue to allow
increases. However, modeling this
approach showed that it would reward
those organizations with exceptionally
high risk score growth while penalizing
organizations that do not engage in
efforts to more completely and
accurately code since their risk score
growth could go negative if they did not
code sufficiently intensively.
A model that uses beneficiary
demographic factors alone would avoid
this issue, and may be simpler
administratively precisely because it
employs a more restricted range of
factors. We have therefore also
considered implementing the MA ‘‘new
enrollee’’ demographic risk adjustment
model. This model includes
adjustments for age, sex, Medicaid
enrollment status and originally
disabled status. Such a model, however,
would not take into account the health
status of the assigned beneficiaries
which could have a particularly adverse
effect on ACOs that include providers
and suppliers that typically treat a
comparatively sick beneficiary
population, including academic medical
centers and tertiary care centers.
Therefore, we are proposing to adjust
Medicare expenditure amounts by
employing the CMS–HCC model used in
the MA program.
The CMS–HCC model more
accurately predicts health care
expenditures than the demographic-
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only model as it accounts for variation
in case complexity and severity. In
addition, incorporating diagnosis data
in the risk adjustment model will
encourage ACOs to maintain complete
and accurate medical documentation
which could result in better information
for population management, care
coordination, and quality improvement.
ACOs will have an incentive to code
more completely and accurately, as is
the case with MA plans, and behaviors
such as these could allow an ACO to
achieve apparent savings by coding
changes alone and without improved
methods of beneficiary care. We do not
want to create an environment that
rewards ACOs for achieving apparent
savings by coding changes alone.
Additionally, we expect the ACO’s
average population risk scores to be
stable over time, given that there is
stability in ACO participants and
therefore case mix and we will have
calculated the benchmark risk
adjustment score for the ACO’s
historically assigned beneficiary
population under conditions when the
ACO providers/suppliers would not
have an incentive to increase coding. As
a result, we believe the benchmark risk
adjustment score for the ACO’s
historically assigned beneficiary
population will be a reasonable
approximation of the actual risk score
for the beneficiary population assigned
to the ACO during the agreement
period, while avoiding any distortion
due to changes in coding practices.
Therefore, we propose to calculate a
single benchmark risk score for each
ACO. The same risk score will then be
applied throughout the agreement
period to the annual assigned patient
populations per capita expenditures for
assigned beneficiaries. The benchmark
risk score will be calculated by applying
the CMS–HCC model to the assigned
beneficiary population attributed in
each year of the 3-year benchmark.
However, changes in the assigned
beneficiary population risk score from
the 3-year benchmark period during the
performance year will not be
incorporated. By not incorporating the
effects of changes in coding intensity
during the performance years (versus
the benchmark), we will protect the
program from costs due to greater
diagnosis coding intensity in ACOs.
We welcome comments on this
proposal including comments on
alternative approaches such as using the
MA ‘‘new enrollee’’ demographic risk
adjustment model for risk adjusting in
the Shared Savings Program or applying
a coding intensity cap on annual growth
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in the risk scores of an ACO’s assigned
beneficiary population.
We intend to monitor and evaluate
the issue of more complete and accurate
coding as we gain experience with the
Shared Savings Program, and would
consider making revisions and
adaptations to the final risk adjustment
model through future rulemaking if they
are warranted. Further, to assure the
appropriateness of ACO coding
practices and our methodology for risk
adjusting, we are also proposing to
retain our option to audit ACOs
especially those ACOs with high levels
of risk score growth relative to their
peers and adjust the risk scores used for
purposes of establishing the 3-year
benchmark accordingly. We seek
comment on this proposal.
5. Technical Adjustments to the
Benchmark: Impact of IME and DSH
Section 1899(d)(1)(B)(ii) of the Act
states that ‘‘Such benchmark shall be
adjusted for beneficiary characteristics
and such other factors as the Secretary
determines appropriate * * *.’’ Several
factors in the Medicare FFS payment
systems can affect an ACO’s ability to
realize savings by adjusting payment
rates and thus affecting both
expenditures during the benchmark
period and each subsequent
performance year. Additionally, changes
in these payment factors, between the
benchmark and performance years can
also influence whether an ACO realizes
savings or incurs losses under the
program.
Teaching hospitals receive additional
payment to support medical education
through an indirect medical education
(IME) adjustment. In addition, hospitals
that serve a disproportionate share of
low-income beneficiaries also receive
additional payments, referred to as the
Medicare disproportionate share
hospital (DSH) adjustment. Many
hospitals, especially academic medical
centers, receive both these adjustments,
which can provide substantial increases
in their Medicare payments compared to
hospitals that do not qualify for these
adjustments. The higher payments
provided to these types of hospitals
could provide ACOs with a strong
incentive to realize savings simply by
avoiding referrals to hospitals that
receive IME and DSH payments.
We have considered whether it would
be appropriate to remove IME and DSH
payments or a portion of these payments
from the benchmark and the calculation
of actual expenditures for an ACO.
However, section 1899(d)(1)(B)(i) of the
Act only provides authority to adjust
expenditures in the performance period
for beneficiary characteristics and does
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not provide authority to adjust for ‘‘other
factors’’. Therefore, while we may adjust
the benchmark under this provision by
removing IME and DSH payments, we
could not also do so in our calculation
of performance year expenditures. If we
were to remove IME and DSH payments
from the benchmark, the benchmark
would be set artificially lower relative to
the performance period, thus making it
more difficult for an ACO to overcome
and achieve savings under this program.
In addition, excluding these payments
would result in an artificial and
incomplete representation of actual
spending of Medicare Trust Fund
dollars. Further, section 1899(d)(1)(B)(ii)
of the Act requires that we update an
ACO’s benchmark during each year of
the agreement period based on a
national standard (‘‘the projected
absolute amount of growth in national
per capita expenditures for parts A and
B under the original Medicare fee-forservice program’’), which would
necessarily include the effects of these
payments. Additionally, we believe all
relevant Medicare costs should be
included in an ACO’s benchmark to
maintain sufficient incentives for ACOs
to ensure their assigned beneficiaries
receive care in the most appropriate
settings. For example, ACOs that
include teaching and/or DSH hospitals
in their network might be more
interested in joining the program if we
do not remove these payments from the
calculations. This is because including
these payments would result in higher
benchmarks against which such ACOs
would work to achieve savings, and
such ACOs may be able to earn back a
portion of forgone IME/DSH payments
in the form of shared savings in cases
where a referral to a less intensive
setting is most appropriate for the
beneficiary.
Thus, we are not proposing to remove
IME and DSH payments from the per
capita costs included in the benchmark
for an ACO. However, we invite
comments on this issue, especially on
how including or excluding these
payments in the benchmark could likely
affect access to medically necessary
services provided at teaching/DSH
hospitals. We will consider comments
on this issue carefully, and in the light
of these comments, we could adopt a
policy in the final rule of adjusting the
benchmark calculation in order to
prevent any adverse effects on access to
services at these hospitals.
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6. Technical Adjustments to the
Benchmark: Impact of Geographic
Payment Adjustments on the
Calculation of the Benchmark
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Similarly, another factor in the
Medicare FFS payment systems that
could affect an ACO’s ability to realize
savings is the geographic payment
adjustment (for example, the IPPS wage
index adjustments and the physician fee
schedule geographic practice cost index
(GPCI) adjustments) that is generally
made to payments under these systems.
These adjustments increase and
decrease payments under these systems
to account for the different costs of
providing care in different areas of the
country. Further, there have been a
number of temporary legislative
adjustments to the wage indexes for
various parts of the country during
recent years. In some cases these have
been extended on virtually an annual
basis while others have been updated
more intermittently. The timing of these
adjustments could result in changes
being made during an ACO’s agreement
period and between the benchmark and
the performance years, thus influencing
an ACO’s ability to realize savings
under the program.
As in the case of IME and DSH
adjustments, we have considered
removing these geographic payment
adjustments from the calculation of the
benchmark and actual expenditures.
However, as with IME and DSH
payments, we only have statutory
authority under section 1899(d)(1)(B) of
the Act to remove them from the
benchmark and thus we cannot remove
them from performance period
expenditure calculations. Consistent
with our proposed treatment of IME and
DSH payments, we are not proposing to
remove geographic payment
adjustments from the calculation of
benchmark expenditures. Again, we
welcome comments on this issue and
will especially consider comments on
the likely impact of this proposal in
areas that are affected by temporary
geographic adjustments. After
consideration of the comments, we
could adopt a policy in the final rule of
adjusting the benchmark calculation to
remove the effects of these geographic
payment adjustments.
7. Technical Adjustments to the
Benchmark: Impact of Bonus Payments
and Penalties on the Calculation of the
Benchmark and Actual Expenditures
Medicare bonus payments are
available and penalties may be imposed
through value-based purchasing
initiatives such as the Physician Quality
Reporting System and the Health
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Information Technology for Economic
and Clinical Health (HITECH) Act,
which encourages hospital and
physician adoption of electronic health
records (EHR), and provides for
penalties in subsequent years for those
that do not demonstrate meaningful use
of EHR. Incentive payments for
programs such as these can affect actual
expenditures and the benchmark, and
thus an ACO’s ability to realize savings.
For example, an ACO’s chances to share
in savings or the level of savings that
would be shared with the ACO would
be reduced when an ACO professional
or hospital participating in the ACO
fails to receive an incentive payment (or
is penalized with a payment reduction)
under one of these programs during a
benchmark year and subsequently
receives an incentive payment from that
program in an ACO performance year.
This is because, all else being equal—
(1) the ACO’s expenditures in the
performance year would be higher than
they would have been in the absence of
the incentive; and (2) the ACO’s
expenditures during the benchmark year
would be relatively lower than they
would have been had an incentive been
received. Conversely, an ACO would be
more likely to share in savings if it
received an incentive payment under
one of these other programs in a
benchmark year and received no
incentive or was penalized during a
performance year. As such, the effect of
including these incentive payments in
the calculation of the benchmark and
actual expenditures could create
perverse incentives with the result that
participation in the Shared Savings
Program has the potential to adversely
affect the performance of providers of
services and suppliers with respect to
other important Medicare efforts, such
as the value-based purchasing and
HITECH initiatives.
Section 1899(b)(3)(D) of the Act
provides authority for the Secretary to
incorporate, as the Secretary determines
appropriate, the reporting requirements
and incentive payments related to the
Physician Quality Reporting System,
eRx, EHR, and other similar initiatives
under section 1848 of the Act. The
statute provides that these incentive
payments ‘‘shall not be taken into
consideration when calculating any
payments otherwise made under
subsection (d).’’ Additionally, we
believe it is important to ensure that
these various programs’ incentives are
properly aligned so that their
interactions support rather than impede
each of the programs’ goals.
Thus, consistent with our statutory
authority, we are proposing to exclude
Medicare expenditures or savings for
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incentive payments and penalties under
section 1848 of the Act for value-based
purchasing initiatives such as Physician
Quality Reporting System, eRx, and the
EHR incentives for eligible professionals
under the HITECH Act from the
computations of both benchmark and
actual expenditures during the
agreement period. We believe that
excluding these costs and savings will
reduce the chances that incentives that
were intended to encourage and reward
participation in one Medicare program
would discourage full participation in
another. We seek comments on this
proposal.
Section 1899(b)(3)(D) of the Act does
not, however, provide authority for the
Secretary to exclude Medicare
expenditures or savings for incentive
payments and penalties not under
section 1848 of the Act from benchmark
and actual expenditures. Therefore,
payments that are reflected in Part A
and B claims for services furnished to
assigned FFS beneficiaries, such as EHR
incentive payments to hospitals and the
Hospital Inpatient Value-Based
Purchasing Program, which are made
under section 1886 of the Act, and EHR
incentive payments to CAHs, which are
made under section 1814 of the Act, (or
any incentive payments not made under
section 1848 of the Act) would be
counted in both the computation of
actual expenditures and benchmark
expenditures for Part A and B costs.
8. Trending Forward Prior Years’
Experience To Obtain an Initial
Benchmark
Section 1899(d)(1)(B)(ii) of the Act
requires the use of ‘‘the most recent 3
years of per-beneficiary expenditures for
parts A and B services’’ to estimate a
benchmark for each ACO. As the statute
requires the use of historical
expenditures, the per capita costs for
each year must be trended forward to
current year dollars and then averaged
using the weights previously described
to obtain the benchmark for the first
agreement period. This benchmark is
subsequently updated for each year of
the agreement period based on the
‘‘projected absolute amount of growth in
national per capita expenditures for
parts A and B services’’ under the FFS
program as estimated by the Secretary.
a. Flat Dollar vs Growth Rate as a
Benchmark Trending Factor
The statute does not specify the
trending factor to be used in estimating
the initial benchmark. Typically, prior
years would be increased using a
percentage growth factor. We
considered two options for trending
forward the most recent 3 years of per
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beneficiary expenditures for Parts A and
B services in order to estimate the
benchmark for each ACO. The first
option is to trend these expenditures
forward using growth rates in
expenditures for Parts A and B services
for FFS beneficiaries. The second option
is to trend these expenditures forward
using a flat dollar amount equivalent to
the absolute amount of growth in per
capita expenditures for Medicare Parts
A and B under the FFS program.
An advantage of the first option is that
the use of a growth rate, as opposed to
a flat dollar amount, would more
accurately reflect each ACO’s historical
experience. That is, in contrast to a flat
dollar amount, this option would
neither raise the bar for ACOs in
historically higher growth rate areas nor
lower it for ACOs in lower growth areas.
At the same time, it could be argued that
this option perpetuates current regional
differences in medical expenditures. An
advantage of the second option, using
the flat dollar amount equivalent to the
absolute amount of growth in per capita
expenditures for Medicare Parts A and
B under the FFS program, is that it is
more consistent with the method
designated by the under section
1899(d)(1)(B)(ii) of the statute for
updating the benchmark (as described
later in this proposed rule) during the
agreement period. This option also
provides a stronger incentive for ACO
development in areas with historically
lower expenditures and growth rates.
Conversely, potential ACOs in areas
with historically higher growth rates
could be reluctant to participate in the
program because the challenge to reduce
their growth rate would be greater in
these areas relative to low expenditure,
low growth ones.
On balance, we believe that for
purposes of establishing an initial
expenditure benchmark, expenditures
should be trended forward in a
relatively neutral and comparable way
across geographic areas. Therefore, we
are proposing to trend forward the most
recent 3 years of per-beneficiary
expenditures using growth rates in per
beneficiary expenditures for Parts A and
B services. For example, we would use
2011, 2012 and 2013 claims year data to
set the benchmark for an ACO starting
its agreement period in 2014. The 2011
and 2012 data would be trended
forward using the factor described later
in this proposed rule so that all
benchmark dollars would be in 2013
dollars. We welcome comments on this
proposal, and especially on whether the
other option that we considered to trend
the benchmark by the flat dollar amount
would be more consistent with our
proposal to update the benchmark as
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specified under section 1899(d)(1)(B)(ii),
as discussed in the next section.
b. National vs Local Growth Rate as a
Benchmark Trending Factor
Under the option described
previously, we could trend per
beneficiary expenditures forward using
national or local growth factors. Using
the national growth rate in Medicare A
and B FFS expenditures would appear
to be more consistent with the
methodology that, as specified in
section 1899(d)(1)(B)(ii) of the Act
incorporates the absolute amount of
growth in per capita expenditures for
Medicare Parts A and B nationwide
under the FFS program in updating each
ACO’s benchmark. A national growth
rate would allow a single growth factor
to be applied to all ACOs regardless of
their size or geographic area. However,
a national rate could also
disproportionately encourage the
development of ACOs in areas with
historical growth rates later in this
proposed rule the national average that
would benefit from having a relatively
higher base, which increases the
chances for shared saving, while
relatively discouraging development of
ACOs in areas with historically higher
growth rates above the national average
that would have a relatively lower base.
In contrast, trending expenditures
based on State or local area growth rates
in Medicare A and B expenditures may
more accurately reflect the experience
in an ACO area and mitigate differential
incentives for participation based on
location. Therefore, we considered an
option to trend the benchmark by the
lower of the national projected growth
rate or the State or the local growth rate.
This option would balance providing a
more accurate reflection of local
experience with not rewarding
historical growth higher than the
average. This method also instills strong
saving incentives for ACOs in both highcost growth and low-cost growth areas.
After considering both of these
alternatives, we are proposing to employ
the national growth rate in Medicare
Parts A and B expenditures for FFS
beneficiaries for trending forward the
fixed benchmark. We believe this
approach will help to ensure that ACOs
in both high spending, high growth and
low spending, low growth areas will
have appropriate incentives to
participate in the Shared Savings
Program, while also moving toward
establishing a national standard for
calculating and measuring ACO
financial performance. We seek
comment on this proposal and on the
alternatives to using a national growth
rate as outlined previously.
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9. Updating the Benchmark During the
Agreement Period
Section 1899(d)(1)(B)(ii) states that
the benchmark shall be ‘‘updated by the
projected absolute amount of growth in
national per capita expenditures’’. We
believe that Congress demonstrated an
interest in mitigating some of the
regional differences in Medicare
spending among ACOs by requiring the
use of a flat dollar amount equivalent of
the absolute amount of growth in
national FFS expenditures to update the
benchmark for the agreement period. In
effect, in the second and third years of
an agreement period, using a flat dollar
increase, which would be the same for
all ACOs, provides a relatively higher
expenditure benchmark for low growth
low spending ACOs and a relatively
lower benchmark for high growth high
spending ACOs. All else being equal, an
ACO can more likely share in savings
when its actual expenditures are judged
against a higher, rather than a lower
benchmark. Thus, with a flat dollar
increase to the benchmark, ACOs in
high cost high growth areas must reduce
their rate of growth more to bring their
costs more in line with the national
average.
However, we also considered our
authority under Section 1899(i) for an
alternative option. Specifically, we
considered an option to update the
benchmark by the lower of the national
projected absolute amount of growth in
national per capita expenditures or the
local/State projected absolute amount of
growth in per capita expenditures.
Incorporating more localized growth
factors reflects the expenditure and
growth patterns within the geographic
area served by ACO participants and
ACO providers/suppliers, potentially
providing a more accurate estimate of
the updated benchmark based on the
area from which the ACO derives its
patient population. Capping the update
at the projected absolute amount of
growth in national per capita
expenditures prevents the update from
disproportionately allowing relatively
larger dollar-amount updates for highspending areas that potentially have a
stronger ability to improve care
coordination and efficiency from
current levels. Not using the national
flat-dollar update for low-spending,
low-growth areas ensures that the
Medicare Shared Savings Program
instills strong saving incentives for
ACOs in low-cost areas, as well as for
those in high-cost areas. Also, as noted
in section V.C.1. of this proposed rule,
using the national flat-dollar update as
specified in section 1899(d)(1)(B)(ii) for
all ACOs could contribute to selective
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program participation that could result
in Medicare costs due to an increase in
the amount of bonus payments for
unearned savings.
In keeping with section
1899(d)(1)(B)(ii) of the Act, we are
proposing to update the benchmark by
the projected absolute amount of growth
in national per capita expenditures. We
believe this approach will help to
ensure that ACOs in both high
spending, high growth and low
spending, low growth areas will have
appropriate incentives to participate in
the Shared Savings Program. We seek
comment on this proposal and on the
alternative to update by the lower of the
national projected absolute amount of
growth in national per capita
expenditures or the local/State projected
absolute amount of growth in per capita
expenditures under section 1899(i) of
the Act.
10. Minimum Savings Rate (MSR) and
Sharing Rate
Section 1899(d)(1)(B)(i) of the Act
provides that ‘‘an ACO shall be eligible
to receive payment for shared savings
under paragraph (2) only if the
estimated average per capita Medicare
expenditures under the ACO for
Medicare fee-for-service beneficiaries
for parts A and B services, adjusted for
beneficiary characteristics, is at least the
percent specified by the Secretary below
the applicable benchmark * * *.’’ That
provision further states that the
‘‘Secretary shall determine the
appropriate percent * * * to account
for normal variation in expenditures
under this title, based upon the number
of Medicare fee-for-service beneficiaries
assigned to an ACO.’’ Section
1899(d)(1)(B)(ii) of the Act provides
that, if an ACO has savings in excess of
the MSR and meets the quality
standards established by the Secretary,
‘‘a percent (as determined appropriate
by the Secretary) of the difference
between such estimated average per
capita Medicare expenditures in a year,
adjusted for beneficiary characteristics,
under the ACO and such benchmark for
the ACO may be paid to the ACO as
shared savings and the remainder of
such difference shall be retained by the
program under this title.’’
A goal of the Shared Savings Program
is to use a portion of the savings (the
difference between the ACO’s actual
expenditures and the benchmark) to
encourage and reward participating
ACOs for coordinating the care for an
assigned beneficiary population in a
way that controls the growth in
Medicare expenditures for that patient
population while also meeting the
established quality performance
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standards. However, observed savings
can also occur as a result of normal
year-to-year variations in Medicare
beneficiaries’ claims expenditures in
addition to the ACO’s activities. Thus,
even if an ACO engages in no activities
to improve the quality and efficiency of
the services it delivers, in certain cases,
differences between the benchmark
expenditures (updated according to
statute) and assigned patients’
expenditures would be observed during
some performance periods merely
because of such normal variation.
Consequently, the statute requires us to
specify a MSR to account for the normal
variations in expenditures, based upon
the number of Medicare FFS
beneficiaries assigned to the ACO. The
MSR should be set in a way that gives
us some assurance that the ACO’s
performance is a result of its
interventions, not normal variation.
However, we also do not want an
outcome where savings that have been
earned are not recognized.
Establishing an MSR on the basis of
standard inferential statistics that take
into account the size of an ACO’s
beneficiary population provides
confidence that, once the savings
achieved by the ACO exceed the MSR,
the change in expenditures represents
actual performance improvements by
the ACO as opposed to normal
variations.
Under the PGP demonstration, the
MSR was initially set at a flat 2 percent
of the benchmark, regardless of number
of assigned beneficiaries, and PGP
practices received back 80 percent of the
savings achieved in excess of the MSR.
However, in establishing a MSR, section
1899(d)(1)(b)(i) of the Act calls on us to
take into account ‘‘the number of fee-forservice beneficiaries assigned to an
ACO.’’ As such, we would need to apply
statistical sampling techniques to
determine a MSR based on the number
of assigned beneficiaries with some
level of statistical confidence.
The MSR in combination with the
savings rate will determine the amount
of shared savings that an ACO can
receive. For example, fewer savings
would be shared if the MSR were set at
a higher percentage. Conversely, shared
savings would be higher if the MSR
were set at a lower percentage. There are
several policy implications associated
with the methodology used to set the
MSR. A higher MSR would provide
greater confidence that the shared
savings amounts reflect the real quality
and efficiency gains, and offer greater
protection to the Medicare Trust Funds.
However, due to the larger barrier to
achieve savings, a higher MSR could
also discourage potentially successful
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ACOs, especially physician organized
ACOs and smaller ACOs in rural areas,
from participating in the program. In
contrast, a lower MSR would encourage
more potential ACOs to participate in
the program, but would also provide
less confidence that savings are a result
of improvements in quality and
efficiency made by an ACO.
We believe that the most appropriate
policy concerning determination of the
‘‘appropriate percent’’ for the MSR
would achieve a balance between the
advantages of making incentives and
rewards available to successful ACOs
and prudent stewardship of the
Medicare Trust Funds. For the onesided model we are proposing a sliding
scale confidence interval (CI) based on
the number of assigned beneficiaries.
The MSR would be established for each
ACO based on increasing nominal
confidence intervals for larger ACOs so
that an ACO with the minimum 5,000
assigned beneficiaries would have an
MSR based on a 90 percent CI; an ACO
with 20,000 assigned beneficiaries
would have a MSR based on a 95
percent CI and an ACO with 50,000
assigned beneficiaries would have an
MSR based on a 99 percent CI. In
addition, the MSR would not be allowed
to fall below 2 percent for larger ACOs.
An ACO that exceeds its MSR would
be eligible to share up to 50 percent of
the savings in the one-sided model
(based on quality performance), as
discussed in section II.E. of this
proposed rule. Table 6 displays the
minimum savings rate an ACO would
have to achieve before savings could be
shared based on the number of its
assigned beneficiaries.
In order to improve the opportunity
for groups of solo and small practices to
participate in the Shared Savings
Program, we are proposing to vary
confidence intervals by the size of the
ACO, which is determined based on the
number of assigned beneficiaries. In
response to our November 17, 2010 RFI,
many commenters recognized the
prevalence of solo and small practices
and the importance of these providers
for rural areas and for the treatment of
specific patient populations, for
example, individuals with mental
health and substance abuse disorders or
beneficiaries residing in skill nursing
facilities. Many of these commenters
urged us to consider policies and
models that encourage the participation
of solo and small practices and to
address barriers they face in forming
ACOs such as access to up-front capital
to invest in the infrastructure and
resources required to redesign care. One
option that would help accomplish this
would be to vary the confidence
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intervals used to establish MSRs so that
smaller practices would have relatively
lower MSRs. Conversely, in recognition
that they are likely to be already
established, possess prior experience,
and thus better able to achieve savings,
larger ACOs would have their MSRs
based on a higher confidence interval,
resulting in a relatively higher MSR.
The MSRs are estimated to provide
confidence that an ACO with a given
number of beneficiaries and assumed to
be of average national baseline percapita expenditure and expenditure
growth rate would be unlikely to
achieve a shared savings payment by
random chance alone. A specific MSR is
a function of both the number of
assigned beneficiaries and a chosen
confidence interval. Recognizing the
higher uncertainty regarding
expenditures for smaller ACOs and the
desire to encourage participation by
smaller ACOs, for the one-sided model,
we propose to set the confidence
interval to 90 percent for ACOs of 5,000
beneficiaries, resulting in an MSR of 3.9
percent. For ACOs with 20,000 and
50,000 beneficiaries, we propose to set
the confidence interval to 95 percent
and 99 percent, respectively, resulting
in MSRs of 2.5 percent and 2.2 percent.
As ACO size increases from 5,000 to
20,000 (or similarly from 20,000 to
50,000), we propose blending the MSRs
between the two neighboring confidence
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intervals, resulting in the MSRs as
shown in Table 6. We specify an MSR
at both the high and low end of each
range of ACO population size. A
particular ACO would be assigned a
linearly-interpolated MSR given their
exact number of beneficiaries. For
example, an ACO with 7,500
beneficiaries would be assigned an MSR
of 3.3 percent because it lies at the
midpoint between 7,000 and 7,999
beneficiaries, sizes at which the MSR
would be 3.4 percent and 3.2 percent,
respectively. For ACOs serving more
than 60,000 aligned beneficiaries, we
propose that the MSR would not be
allowed to fall below 2 percent. This
lower bound is designed to protect the
shared savings formula from
expenditure reduction due to random
chance that can occur in group claims
due to factors that persist regardless of
a group’s size. This lower bound is also
consistent with the flat 2 percent MSR
we propose to use in the two-sided
model and is the minimum level that
was used in the PGP Demonstration for
groups regardless of size which also
provided a lower MSR for smaller
physician groups participating in the
demonstration.
We considered using a flat 95 percent
confidence interval for organizations
which is a recognized standard for
measuring statistical differences, but as
previously noted, because we believe
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that many smaller physician-driven and
rural ACOs have the potential to
improve the quality and efficiency of
care, we were concerned about the
impact on the ability of these ACOs to
participate in the Shared Savings
Program. We also wanted to protect the
Medicare Trust Funds against large
organizations coming together solely for
purposes of aggregating their number of
assigned beneficiaries in order to have
smaller MSRs to be able to achieve the
minimum required savings levels and
share in savings with little or no actual
improvement in the quality and
efficiency of care provided to
beneficiaries.
The proposed confidence intervals
were determined assuming that the
variation in the per capita expenditure
growth for a particular ACO is equal to
the variation in per capita expenditure
growth nationally. This is not the case
for the majority of ACOs, however, as
regional growth rates tend to vary from
the national average due to a number of
variables. Therefore, the confidence
intervals generated using only the
national expenditure growth variation
overstate the relative confidence
associated with an increasing group
size. This is compensated for in two
ways: (1) The 2 percent floor; and (2)
increasing the confidence interval as
group size increases.
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We welcome comments on the most
appropriate means to establish the MSR
for an ACO, including the appropriate
confidence intervals.
11. Net Sharing Rate
Section 1899(d)(2) calls for us to share
‘‘a percent (as determined appropriate
by the Secretary) of the difference
between such estimated average per
capita Medicare expenditures in a year,
adjusted for beneficiary characteristics
under the ACO and such benchmark for
the ACO.’’ Section 1899(i) of the Act
permits the Secretary to consider other
payment models if she determines that
they will ‘‘improve the quality and
efficiency of items and services
furnished under this title’’ and will not
result in additional expenditures. Thus,
in considering the amount of savings
ACOs under the one-sided model could
be eligible to receive, we considered
several options in addition to the
methodology outlined in section
1899(d)(2) of the Act.
The first option we considered is the
one required under section 1899(d)(2) of
the Act, which would permit the ACO
to share on first dollar savings once the
MSR was exceeded. This option would
maximize the reward that an ACO could
realize. This amount could provide
critical financial support for ACOs that
serve a smaller population (for example,
less than 10,000 assigned beneficiaries),
which may be physician only and/or
predominantly care for underserved
populations, or ACOs whose
beneficiaries rely upon safety net
providers for care or ACOs which serve
rural areas. However, given the normal
variation in expenditures, we have
concerns that sharing on first dollar
could result in sharing on unearned
savings rather than on savings achieved
by the ACO for redesigned care
processes.
Therefore, we considered another
alternative which would be to limit the
amount of savings by requiring ACOs to
exceed the MSR and then share with the
ACO only those savings in excess of the
MSR. As discussed in the previous
section, one challenge to appropriate
sharing of savings under this program is
that observed savings can occur as a
result of normal year-to-year variations
in Medicare beneficiaries’ claims
expenditures in addition to the ACO’s
activities. This concern is heightened in
the one-sided model, because absent
initial accountability for losses, ACOs
have less motivation to eliminate
unnecessary expenses and may be more
likely to be rewarded as a result of
methodological requirements. Sharing
only in savings which exceed the MSR
is consistent with the design of the
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original PGP demonstration and would
reduce the probability that shared
savings are earned as a result of chance
or lower pre-existing expenditure trends
due to existing efficiencies, and not
newly enhanced care coordination and/
or redesigned delivery of care. Further,
such a requirement would encourage
ACOs to strive to generate greater levels
of savings.
A third option we considered would
be to require all ACOs to exceed the
MSR to be eligible for savings, but only
share savings in excess of a certain
threshold. ACOs meeting certain criteria
could be exempted from this provision
and be allowed to share in first dollar
savings. This option would balance the
need to have assurance that savings are
not a result of random variation with the
need to provide critical financial
support for under-funded ACOs,
particularly ACOs that serve a smaller
population, safety net providers, or
physician-only participants.
Additionally, we have experience with
this model through the PGP
demonstration.
We are proposing the third option,
that is, we propose that once an ACO
has surpassed its MSR, the ACO would
share in savings beyond a certain
threshold. We further propose that,
unless exempted, ACOs that exceed the
MSR would be eligible to share in net
savings above a 2-percent threshold,
calculated as 2 percent of its benchmark
(updated according to statute). The
sharing rate (earned quality performance
sharing rate and additional increases for
including FQHCs and/or RHCs) would
be applied to net savings above this
2 percent threshold in order to
determine the shared savings amount.
We believe that this threshold protects
the program from sharing unearned
savings and helps to ensure that shared
savings are due to enhanced care
coordination and quality of care on the
part of the ACO.
As previously discussed, many
smaller physician-driven ACOs and
ACOs caring for underserved
populations have the potential to
improve the quality and efficiency of
care, but may be especially challenged
in accessing capital to meet their needs.
We hope to encourage successful
participation by these ACOs in the
Shared Savings Program. Additionally,
we acknowledge that providers/
suppliers working in these
environments face additional challenges
in coordinating care and creating the
infrastructure necessary to create a
successful ACO, and therefore may not
be equipped to assume the risk right
away (and be eligible for greater reward)
of the two-sided model. As such, we are
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proposing that ACOs that meet the
following criteria would be exempt from
the 2 percent net savings threshold and
would instead share on first dollar
savings under the one-sided model. We
propose to exempt ACOs with less than
10,000 assigned beneficiaries in the
most recent year for which we have
complete claims data (for instance, 2012
for 2014 program participation) and that
meet one of the following:
• The ACO is comprised only of ACO
professionals in group practice
arrangements or networks of individual
practices of ACO professionals.
• 75 percent or more of the ACO’s
assigned beneficiaries reside in counties
outside a Metropolitan Statistical Area
(MSA) in the most recent year for which
we have complete claims data.
• 50 percent or more of the ACO’s
assigned beneficiaries were assigned to
the ACO on the basis of primary care
services received from a Method II CAH.
• 50 percent or more of the
beneficiaries assigned to the ACO had at
least one encounter with an ACO
participant FQHC and/or RHC in the
most recent year for which we have
complete claims data, that is, the ACO
has met criteria for receiving full
potential additional payment as
described later in this proposed rule.
We invite comment on these
proposals and the other options
considered.
12. Additional Shared Savings
Payments for Including FQHCs and/or
RHCs
We are also proposing that an ACO in
the one-sided model can receive an
increase in its shared savings rate of up
to 2.5 percentage points during the first
2 years of its agreement, for including a
strong FQHC and/or RHC presence
within the structure of the ACO. (See
section II.G. of this proposed rule for
details surrounding the two-sided
model which provides for a
5 percentage point increase for
including FQHCs or RHCs or both.)
FQHCs and RHCs have long delivered
comprehensive, high-quality primary
health care to patients regardless of their
ability to pay, and increase access to
health care through innovative models
of community-based, comprehensive
primary health care that focus on
outreach, disease prevention, and
patient education activities. FQHCs
provide high-quality care to rural and
urban populations alike by focusing
attention on improving public health
through preventive care in addition to
direct patient care. Not only do health
centers provide critical, high quality
primary care in the Nation’s neediest
areas, but reports have shown that the
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RHCs improve access to primary care
in underserved rural areas through the
use of interdisciplinary team· based
care. Currently, more than 3,800 such
RHCs provide care to more than 1.6
million Medicare beneficiaries
throughout the United States. RHCs
provide critical, quality primary care to
Medicare beneficiaries and others most
in need in underserved areas. Research
has shown that RHCs not only provide
care at costs significantly less than other
providers of care, such as emergency
departments and hospitals, but also
reduce use of those providers.
Additionally, research on RHCs has
shown that:
• Among older adults, the presence of
an RHC in the county reduced
ambulatory care sensitive (ACS)
conditions admission rates, compared to
counties in which an RHC was not
present.16
• RHCs offer financially accessible
care to low income individuals;
96 percent of independent RHCs
surveyed offer free care, sliding fee
scales, or both.17
Accordingly, because FQHCs and
RHCs are unable to participate
independently in this program, we
believe providing incentives to ACOs
that include FQHCs and/or RHCs as
ACO participants is in the interest of the
Shared Savings Program as
incorporation of these types of entities
will promote care coordination and the
delivery of efficient, high-quality health
care. Therefore, we are proposing, for
the one-sided model, up to a 2.5
percentage point increase in the sharing
rate for ACOs that include these entities
as ACO participants. We propose
establishing a sliding-scale payment,
outlined in the following table, based on
the number of Medicare FFS
beneficiaries with one or more visit at
an ACO’s participant FQHC or RHC
during the performance year.
We are also proposing that ACOs
specifically identify their FQHC/RHC
participant TINs in their initial and
annual reporting of ACO participant
TINs, and disclose other provider
identifiers as requested to assure proper
identification of these organizations for
the purpose of awarding the payment
preference.
The statutory definition of FQHCs at
section 1861(aa)(4) of the Act includes
FQHCs receiving grant support under
section 330 of the Public Health Service
Act, so-called FQHC look-a-likes, and
outpatient health programs/facilities
operated by tribal organizations. Our
regulations at 42 CFR 405.2401(b)
include this statutory definition of
FQHCs. Similarly, § 405.2401(b) reflects
the statutory definition of RHCs in
section 1861(aa)(2) of the Act. We
therefore propose to define FQHCs and
RHCs, for the purpose of awarding this
payment preference, as these terms are
defined in § 405.2401(b) of our
regulations. We seek comments on
alternate options for establishing a
payment preference with sliding scale
for ACOs that include FQHCs or RHCs
as ACO participants, including
suggestions for the appropriate method
to measure FQHC/RHC involvement and
the appropriate level of incentives.
We are also interested in encouraging
providers who serve a large portion of
dual eligible beneficiaries to participate
in the Medicare Shared Savings
Program. Medicare beneficiaries who
are also eligible for Medicaid—that is,
are ‘‘dually eligible’’ for these
programs—are among the most
vulnerable of Medicare beneficiaries.
Dual eligible beneficiaries tend to have
higher medical costs than other fee-forservice beneficiaries, and, as a result,
are expected to benefit even more than
other beneficiaries from improvements
in the quality and efficiency of their
care resulting from the greater care
coordination offered by an ACO. The
Affordable Care Act recognizes the
unique status of dual eligible
beneficiaries and includes several
provisions to address their special
15 Falik M. et al. Comparative Effectiveness of
Health Centers as Regular Source of Care. Journal
of Ambulatory Care Management 2006; 29(1):
24–35.
16 Probst, J.C., Laditka, J., and Laditka, S. (2009).
‘‘Community Health Center and Rural Health Clinic
Presence Associated With Lower County-Level
Hospitalization Rates for Ambulatory Care Sensitive
Conditions.’’ South Carolina Rural Health Research
Center.
17 Hartley, D., Gale, J. Leighton, A. and
Bratesman, S. (2010). ‘‘Are Rural Health Clinics Part
of the Rural Safety Net?’’ Muskie School of Public
Service; Maine Rural Health Research Center.
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health center model of care can reduce
the use of costlier providers of care,
such as emergency departments and
hospitals. Currently, more than 1,100
such health centers operate over 7,900
service delivery sites that provide care
to nearly 19 million patients in every
State, the District of Columbia, Puerto
Rico, the U.S. Virgin Islands, and the
Pacific Basin.
Despite serving less healthy and more
vulnerable populations, research
indicates that these health centers have
achieved considerable success in
increasing access to care, improving
health outcomes for patients, reducing
health disparities, and containing health
care costs. For example, regarding
FQHCs, data show health center
Medicaid patients were 11 percent less
likely to be inappropriately hospitalized
and 19 percent less likely to visit the
emergency room inappropriately than
Medicaid beneficiaries who had another
provider as their usual source of care.15
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needs. For instance, section 2602 of the
Affordable Care Act established a
Federal Coordinated Health Care Office
within CMS to bring together officers
and employees of the Medicare and
Medicaid programs at CMS to: (1) more
effectively integrate benefits under the
Medicare and Medicaid programs; and
(2) improve the coordination between
the Federal government and States for
individuals eligible for benefits under
both such programs in order to ensure
that these individuals receive full access
to the items and services to which they
are entitled under titles XVIII and XIX
of the Act.
Additionally section 1899(j) of the Act
provides that ‘‘[t]he Secretary may give
preference to ACOs who are
participating in similar arrangements
with other payers.’’ The statute
prescribes neither the kind of preference
that the Secretary should provide to
such ACOs nor what other types of
arrangements should be considered
‘‘similar’’ for purposes of such a
preference. We believe that the more
patients an ACO sees for which it is
eligible to receive performance-based
incentives, such as shared savings, the
more likely it is that the ACO will adopt
substantial behavior changes conducive
to improved quality and cost savings.
We are seeking comment on methods
to provide preference to ACOs that serve
a large dual-eligible population or that
enter and maintain similar arrangements
with other payers. Specifically we seek
comment regarding suggestions to
encourage accountability for dualeligible beneficiaries and participation
in similar arrangements with other types
of payers.
13. Withholding Performance Payments
To Offset Future Losses
Over the course of the program, an
ACO may earn performance payments
in some years and incur losses in other
years. The issue is whether the full
amount of shared savings payments
should be paid in the year they are
accrued, or whether some portion
should be withheld to offset potential
future losses. For example, under the
PGP demonstration, a flat 25 percent
withhold applied to annual earned
performance payments to guard against
losses in future years as well as to
provide an incentive for PGPs to
continue in the demonstration since the
withhold was only released at the end
of the demonstration period or when the
PGPs were rebased. Under the two-sided
model discussed in section II.G. of this
proposed rule, we propose that an ACO
may use a withhold of their earned
shared savings payment as one option
for demonstrating an adequate
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repayment mechanism in the event they
incur shareable losses. As discussed in
sections II.B. and II.I. of this proposed
rule, we believe the requirement that
ACOs be willing to commit to a 3-year
agreement to participate in the Shared
Savings Program is necessary to ensure
that the program achieves its long-term
goal of redesigning health care
processes, and our proposal here
furthers that intent. Since we want to
encourage ACOs to participate for all 3
years of their agreements, protect the
Medicare program against losses, and
ensure ACOs have an adequate
repayment mechanism in the event they
incur losses under either the one-sided
or two-sided model, we are proposing a
flat 25 percent withholding rate will be
applied annually to any earned
performance payment. Under the twosided model as discussed in Section
II.G. of this proposed rule, we propose
that an ACO may withhold an
additional portion of its earned
performance payment as a mechanism
to demonstrate an adequate repayment
mechanism in the event they incur
shareable losses. Furthermore, we
propose that at the end of each
agreement period, positive balances will
be returned to the ACO. However, if the
ACO does not complete its 3-year
agreement, the ACO would forfeit any
savings withheld.
14. Performance Payment Limit
Section 1899(d)(2) of the Act requires
the Secretary to ‘‘establish limits on the
total amount of shared savings that may
be paid to an ACO * * *.’’ Therefore,
we must propose the maximum
performance payment an ACO may
receive in any given performance year
in this proposed rule. In determining
what would constitute an appropriate
limit, we believe that it should provide
a significant opportunity for ACOs to
receive shared savings generated from
quality improvements and better
coordination and management of Part A
and B services, while avoiding creating
incentives for excessive reductions in
utilization which could be harmful to
beneficiaries. Under the PGP
demonstration, the limit was set at 5
percent of the organization’s Part A and
Part B expenditure target.
For purposes of the Shared Savings
Program, we considered an option to
vary the performance payment limit by
the readiness of the ACO to take on
greater responsibility and risk. ACOs
seeking to participate in the Shared
Savings Program will vary with respect
to their readiness to function under a
risk model with respect to their
organizational and systems capacity and
structure. Accordingly, some ACOs
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might more quickly be able to
demonstrate quality improvements and
savings than will others. Applying
differential payment limits based on an
ACO’s readiness to take on risk could be
another means to encourage and reward
successful ACO participation.
In light of our experience with the
PGP demonstration, we considered a
limit of 5 percent. We also considered
whether a higher limit, such as 10
percent or 15 percent, would be
appropriate to provide an even stronger
incentive for ACOs to develop the
quality and efficiency improvements
that could result in greater shared
savings. Depending on an ACO’s
composition, shared savings payments
under such higher limits could
represent an even larger portion of
Medicare payments to ACO participants
for care furnished to assigned
beneficiaries since the cap is a
percentage of the ACO’s benchmark for
Medicare Part A and B expenditures for
assigned beneficiaries, which reflects all
care furnished to those beneficiaries,
regardless of whether it was provided in
the ACO. For example, an ACO that
does not include a hospital would have
the opportunity to realize a relatively
higher proportion of shared savings as a
percentage of its Medicare revenue by
reducing Part A expenditures for its
assigned beneficiaries. However,
opportunities to earn greater savings
could also raise questions about
whether the quality of care is
improving, which is a goal as important
as achieving savings in the Shared
Savings Program. Providing an incentive
for ACOs to invest to improve quality
and efficiency of care needs to be
balanced against providing an overly
large incentive where an ACO may be
encouraged to generate savings resulting
from inappropriate limitations on
necessary care. A higher cap on total
shared savings could provide such an
incentive to limit care. While all ACOs
may have this incentive to some degree,
ACOs without Part A providers could
have greater incentive to do so,
depending on where the cap is
established.
A lower limit, such as the 5 percent
limit under the PGP demonstration,
would reward ACOs for improving
quality and efficiency and potentially
generate more savings for the Medicare
program without creating incentives to
limit care that is appropriate and
necessary. On the other hand, a lower
limit might be an insufficient incentive
for some potential ACOs to participate
in the program. In contrast, a higher
percentage limit, such as 10 or 15
percent of an ACO’s Part A and B
expenditure benchmark, would provide
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greater incentives for organizations to
participate in the program and to
achieve the quality and efficiency gains
that are the goals of the Shared Savings
Program. Many health care researchers
believe that the rate of unnecessary
health care is more than the
approximate 10 percent which would be
implied by establishing a 5 percent cap
on ACO shared savings. (Since the
maximum shared savings potentially
realized by an ACO under the one-sided
model is 52.5 percent, a 7.5-percent
limit on the ACO share implies an
expectation that overall savings may be
as high as approximately 14 percent; a
10-percent limit implies a savings
expectation of approximately 19
percent.) On the other hand, such a
higher limit may provide some
incentive for ACO providers/suppliers
to reduce utilization inappropriately,
which could potentially be harmful to
beneficiaries
We believe that the considerations in
favor of both a lower (for example, 5
percent) and a higher (for example, 10
percent) limitation on shared savings
with an ACO have merit. Accordingly
we are proposing to establish the
payment limit at 7.5 percent of an
ACO’s benchmark for the first 2 years of
the agreement under the one-sided
model. Following suggestions by
MedPAC, in order to encourage ACOs to
assume risk and participate in the twosided model, as described in section
II.G. of this proposed rule, we are
proposing, for the two-sided model, to
establish the payment limit at 10
percent of an ACO’s benchmark for
those ACOs that either elect the twosided model initially for all 3 years or
are transitioned from the one-sided
model during the third year of their
agreement period. (Since the maximum
shared savings potentially realized by
an ACO under the two-sided model is
65 percent, a 10-percent limit on the
ACO share implies an expectation that
overall savings may be as high as
approximately 15 percent). We are
soliciting comments on these proposed
payment limits and on whether a higher
limit—for example, 10 percent for all
ACOs—would be more appropriate in
the light of the considerations discussed
previously and other considerations that
commenters may wish to raise. We also
seek comments on whether differential
limits should be established based on an
ACO’s readiness, as discussed
previously, including the criteria we
would apply and the methods by which
we would assess readiness and how
differential limits should be structured.
We will consider this information and
the implications for a differential cap
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based on ACO readiness in future
rulemaking cycles.
Regardless of what limit is adopted in
the final rule, we plan to monitor
beneficiary access and utilization of
services, and the potential contribution
of the performance limit to any
inappropriate reductions in services.
Our proposals related to monitoring and
addressing ACO performance can be
found in Section II.H. of this proposed
rule. Furthermore, as we gain more
experience with the Shared Savings
Program and are able to evaluate how
well the incentive structure under the
Shared Savings Program is operating to
generate greater quality and efficiency
without inappropriately reducing
utilization of services, we may
undertake additional rulemaking to
revise the performance payment limits
we establish in the final rule.
G. Two-Sided Model
Section 1899 of the Act implements a
voluntary program that provides
incentives for group of providers of
services and suppliers to work together
to improve the quality and efficiency of
care for a FFS beneficiary population in
exchange for a share in any savings
generated from their effort. Section
1899(i) of the Act authorizes the
Secretary to use other payment models
in addition to the shared savings model
outlined in section 1899(d) of the Act
under which we only share savings with
ACOs. This provision authorizes the
Secretary to select a partial capitation
model or any other payment model that
the Secretary determines would
improve the quality and efficiency of
items and services furnished to
Medicare fee-for-service beneficiaries. In
addition, section 1115A of the Act, as
amended by 3021 of the Affordable Care
Act, authorizes the Center for Medicare
and Medicaid Innovation (Innovation
Center) to test innovative payment and
service delivery models, which could
include alternative ACO payment
models.
In the November 17, 2010 Federal
Register, we solicited public comment
on a number of issues including the
types of alternative payment models we
should consider in addition to the
model laid out in section 1899(d) of the
Act, either in the Shared Savings
Program under the authority provided
in 1899(i) of the Act or using the
Innovation Center authority under
section 1115A of the Act. We further
asked about the relative advantages and
disadvantages of any such payment
models.
Most comments received in response
to this question favored our use of
alternative payment models. A number
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of commenters suggested risk-based
models such as partial capitation (an
up-front fixed dollar amount for a subset of Medicare services rendered by a
provider per beneficiary per period of
time) or global payment (an up-front
fixed dollar amount for all Medicarecovered services required per
beneficiary per period of time).
Commenters proposed both one-sided
shared savings models (to ease
providers of services and suppliers into
this payment model) and models that
would allow ACOs to share in savings
and be held accountable for losses (twosided models).
Taking these comments into account,
we are proposing that ACOs could elect
the two-sided model for their initial
agreement period, to become
accountable for losses and in order to be
eligible for higher sharing rates than
would be available under the one-sided
model, beginning in their first
performance year. In addition, we are
also proposing that ACOs that initially
elect the one-sided model would be
reconciled annually for the first 2 years
of the 3-year agreement using the onesided model and automatically
transitioned to the two-sided model for
the third year of their agreement. This
approach gives ACOs an option of two
tracks for their initial agreement period,
thereby providing an opportunity for
organizations more experienced with
care coordination and risk models, that
are ready to accept risk to enter a
sharing arrangement that provides
greater reward for greater responsibility
in year 1, while also providing an entry
point for organizations with less
experience with risk models, such as
some physician-driven organizations or
smaller ACOs, to gain experience with
population management before
transitioning to more risk.
1. Risk-Based Payment Models
In section II.F of this proposed rule,
we describe in detail the one-sided
model, under which ACOs share in
savings but are not accountable for
repaying any losses if actual
expenditures exceed the benchmark.
While we believe this model holds
promise for creating substantial
improvement in quality and cost, many
commenters on the November 17, 2010
RFI, and other stakeholders urged us to
include risk-based arrangements where
ACOs would also be accountable for
downside risk. Policy experts have also
suggested that incorporating downside
risk-based models into the Shared
Savings Program would provide a
stronger lever than a one-sided model
for encouraging ACOs to achieve
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efficiencies and attain the program’s
transformative goals.18
Risk-based arrangements may take
many forms. Two models considered for
inclusion in the Shared Savings
Program were two-sided risk
arrangements (shared savings and
losses) and partial capitation. Realworld examples of these models vary
widely, according to the terms of
specific provider-payer initiatives they
encompass. Partial capitation refers to a
payment system that incorporates
elements of both capitation and FFS.
Section 1899(i) of the Act defines partial
capitation as a model ‘‘* * * in which
an ACO is at financial risk for some, but
not all, of the items and services
covered under Parts A and B, such as at
risk for some or all physicians’ services
or all items and services under Part B.’’
Our intent is to design and test partial
capitation models in the Innovation
Center first in order to gain more
experience, introduce them to providers
of services and suppliers, and refine
them before adopting them more widely
in the Shared Savings Program.
In a two-sided model based around
FFS within the Shared Savings Program,
ACOs would accept the downside risk
for losses once the minimum loss rate is
exceeded (the equivalent of the
minimum savings rate that must be
exceeded in order to share in savings
under the Shared Savings Program).
ACOs’ exposure to downside risk could
also be limited by the creation of risk
corridors that establish a maximum
shared loss cap. We are proposing to
make available a two-sided model in the
Shared Savings Program to foster ACOs’
accountability for greater risk with a
greater opportunity for reward. ACOs
may elect to enter the one-sided model
(Track 1) or elect the two-sided model
(Track 2). An ACO that elects Track 1
would automatically be transitioned to
the two-sided model for the third year
of its agreement. Thus, in the third year
of the ACO’s agreement under Track 1,
the methodology used to reconcile
ACOs under the first year of the twosided model would apply except ACOs
must meet the quality performance
standard that applies in the third year
(as opposed to the first year standard of
full and accurate reporting). A key
attribute of FFS is beneficiary freedom
of choice to choose any provider they
wish which will be maintained under
both the one-sided and two-sided
models.
18 See e.g., Robert A. Berenson, ‘‘Shared Savings
Program for Accountable Care Organizations: A
Bridge to Nowhere?’’ The American Journal of
Managed Care, Vol 16, No. 10 (October 2010).
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There are pros and cons of risk-based
arrangements. Providers of services and
suppliers engaged in a risk-based
payment arrangement, compared to a
one-sided shared savings structure, have
a stronger incentive to control spending
and achieve efficiencies. This is
consistent with the antitrust perspective
that participants in financially
integrated organizations have the
incentive to cooperate in controlling
costs and improving quality by
managing the provision of services; such
that to demonstrate financial
integration, participants in a
collaboration must share substantial
financial risk, as discussed in section
II.B of this proposed rule. Risk-based
arrangements offer payers a chance to
control spending, either through the
recoupment of excess expenditures
(losses) in two-sided risk arrangements,
or through capitated payments.
However, since providers of services
and suppliers have an increased
motivation to control spending and
achieve efficiencies under a risk-based
model, it would be reasonable to
anticipate an increase in negative
incentives such as incentives to stint on
care or undersupply services, shift costs
(for instance through changes in referral
patterns), as well as increased
incentives for providers of services and
suppliers to avoid at risk beneficiaries.
In the 1990’s, California providers’
willingness to take risk led to the rapid
expansion and failure of many undercapitalized risk-bearing physician
organizations. This experience
illustrates that risk-bearing
arrangements have broad implications
for provider relationships (namely
leading to the integration of providers
through mergers and acquisitions); the
financial solvency of provider
organizations and therefore the stability
of health care markets and patients’
access to care; as well as leverage
between providers and private payers.19
For these reasons, risk-based
arrangements require greater assurance
of providers’ financial solvency in order
to repay Medicare for excess
expenditures that may be incurred, as
well as greater beneficiary protections,
for example by heightened monitoring
to detect inappropriate short-cutting of
care and avoidance of at-risk
beneficiaries. In addition, proper
19 See Robert A. Berenson, Paul B. Ginsburg and
Nicole Kemper, ‘‘Unchecked Provider Clout in
California Foreshadows Challenges To Health
Reform’’ Health Affairs, April 2010; James C.
Robinson & Emma L. Dolan, ‘‘Accountable Care
Organizations in California: Lessons for the
National Debate on Delivery System Reform’’
Integrated Healthcare Association, White Paper
(2010).
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safeguards may be needed to address the
risk of conduct violating fraud and
abuse laws.
Incorporation of downside risk into
the Shared Savings Program, while
retaining a FFS base, has been
encouraged by commenters on the
November 17, 2010 RFI (including
MedPAC), other stakeholders and policy
experts as an entry point for moving
ACOs to risk-based arrangements.
MedPAC suggested offering a two-sided
risk model in addition to the one-sided
model, and over time, making the twosided model the dominant or only
option available to program
participants. Further, to encourage
ACOs to participate in the two-sided
model, MedPAC recommended that it
could be distinguished from the onesided model by features such as a larger
share of savings and risk corridors to
protect ACOs from high levels of
losses.20
A relevant example of a two-sided
risk arrangement in a FFS setting is Blue
Cross Blue Shield of Massachusetts’
(BCBSMA) Alternative Quality Contract,
an initiative that engages groups of
providers for HMO or PPO beneficiaries.
Under this contract, providers continue
to be paid on a FFS basis. Each group’s
yearly expenditures are compared
against a predetermined global budget,
factoring in the level of risk the group
has agreed to take on; the group is paid
any surplus or repays BCBSMA for any
deficit. Groups can earn bonuses based
on quality performance targets, and
achieved savings, and also earn
significant quality bonuses.21
Given these considerations, we
believe payment models where ACOs
bear a degree of financial risk hold the
potential to induce more meaningful
systematic change in the behavior of
groups of providers of services and
suppliers compared to a one-sided
model. We propose to develop an option
for an ACO to either enter into a twosided model within the Shared Savings
Program initially or enter into the onesided model within the Shared Savings
Program initially and be transitioned to
the two-sided model in year 3 of its
initial 3-year agreement. We believe this
proposal strikes a balance between
stakeholders’ requests for risk-based
arrangements with the implications for
beneficiary protections and market
stability posed by capitated models and
the operational complexity of creating
20 Letter from Glenn M. Hackbarth, Chairman
MedPAC, to Dr. Donald M. Berwick, Administrator,
Centers for Medicare and Medicaid Services,
November 22, 2010 (File Code CMS–1345–NC).
21 Michael E. Chernew et al. ‘‘Private-Payer
Innovation In Massachusetts: The ‘Alternative
Quality Contract’ ’’ Health Affairs (January 2011).
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these arrangements in a FFS
environment. As we develop experience
with other risk-based models, for
example through the Innovation Center,
we expect to consider incorporating
additional payment models into the
Shared Savings Program through future
rule making.
2. Two Tracks Provide Incremental
Approach to Incorporating Risk
We considered several options about
how to incorporate a two-sided model
into the Shared Savings Program. The
major options we considered are as
follows:
• Basing the program on a two-sided
model, thereby requiring all participants
to accept risk from the first program
year.
• Allowing applicants to choose
between program tracks, either a onesided model or two-sided model, for the
duration of the agreement.
• Allowing a choice of tracks, but
requiring ACOs electing the one-sided
model to transition to the two-sided
model during their initial agreement
period.
Requiring all ACOs to initially take
downside risk would likely inhibit the
participation of some interested entities.
Potential Shared Savings Program
applicants will likely include providers
and suppliers with different levels of
experience with risk-based payment
arrangements and with different levels
of financial footing, reflecting the
heterogeneity of providers and suppliers
and provider arrangements that exist in
the nation’s health care system. The
comments on the November 17, 2010
RFI reflect this diversity, but in sum,
favored our adoption of a flexible
approach that recognizes the different
levels of ACOs’ readiness to take on
risk. For instance, organizations
experienced with integrated care and
risk-based arrangements, with available
financial reserves, may be ready and
willing to accept risk beginning in the
first program year. Others urged against
program requirements which could
preclude small/solo practices and safety
net providers, from entering the Shared
Savings Program. These comments
underscored the scenario in which
ACOs, otherwise capable of meeting the
program’s requirements, may initially
lack the experience and capital to accept
significant downside risk.
However, allowing ACOs to choose
from either a one-sided model or a twosided model also creates some concerns.
Some ACOs capable of taking risk may
take advantage of the option that allows
for gain by realizing savings without any
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risk for incurring added costs. We
believe it important that all Shared
Savings Program participants quickly
move to taking on downside risk. We
believe that payment models where
ACOs bear a degree of financial risk
have the potential to induce more
meaningful systematic change in
providers’ and suppliers’ behavior.
Additionally, by introducing a risk
model, we believe we will elicit
applicants to the program who are more
serious about their commitment to
achieving the program’s goals around
accountability for the care of Medicare
beneficiaries and the three-part aim of
enhancing the quality of health care,
improving patient satisfaction with their
care, and better controlling the growth
in health care costs.
We propose that applicants will have
the option of choosing between a onesided model and a two-sided model
initially. Under Track 1, ACOs enter the
program under the one-sided model and
must transition to the two-sided model
for the third year of their initial
agreement period. Thereafter, those
ACOs can only participate under the
two-sided model for any subsequent
agreement periods. Alternatively, under
Track 2, an ACO may enter the twosided model option immediately for a
full 3-year agreement period. Those
ACOs must also participate in the twosided model thereafter in subsequent
agreement periods. Thus an ACO may
only participate for a maximum of two
years under the one-sided model, during
its first agreement period, before it must
transition and participate thereafter in
the Shared Savings Program under the
two-sided model. We believe that this
approach addresses the concerns we
have identified. Incorporating both a
one-sided and two-sided model into the
Shared Savings Program provides a path
forward for diverse organizations to gain
experience with redesigning care
processes and assuming accountability
for the quality of care and financial
outcomes of the populations they serve.
Requiring those who enter the program
on Track 1 to migrate to the two-sided
model encourages organizations to take
on greater risk with the opportunity for
greater reward. We invite comments on
this proposal and other options for
incorporating a two-sided model into
the Shared Savings Program, including
mechanisms for transitioning ACOs to
two-sided risk arrangements.
3. Elements of the Two-Sided Model
In developing the elements of a twosided model under the Shared Savings
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Program, we propose to employ, as
feasible and appropriate, the elements of
the one-sided model that we have
described in detail in the rest of this
proposed rule. At the same time, it will
be necessary to develop some policies
for the two-sided model that would not
be necessary under a one-sided model,
for example, a methodology for
determining shared losses. In addition,
we believe that it is also appropriate to
adapt some of the elements of the onesided model to the somewhat different
circumstances and incentives under
which ACOs sharing two-sided risk
would operate. Specifically, in light of
the greater potential for a two-sided
model to bring about positive changes in
the operation of the FFS system by
improving both the quality and
efficiency of medical practice, we
believe that it is both appropriate and
essential to provide greater incentives
for organizations that participate in the
two-sided model. For example, as we
describe below, we believe that it is
appropriate to provide a higher shared
savings rate for organizations
participating in the Shared Savings
Program under the two-sided model
than for those organizations
participating under the one-sided
model.
In the discussion that follows, it can
be assumed that the features of the onesided model we have proposed in this
rule would also apply under the twosided model, unless we specifically
state otherwise. In general, we are
proposing the same eligibility
requirements and methodologies for the
two-sided model as we have proposed
for the one-sided model. That is, we
propose to use the same eligibility
criteria, beneficiary assignment
methodology, benchmark and update
methodology, quality performance
standards, data reporting requirements,
data-sharing provisions, monitoring for
avoidance of at-risk beneficiaries, and
transparency requirements under the
two-sided model that we have described
under the one-sided model. However, as
we discuss below, we are adding some
requirements in order to provide further
assurance about the ability of an ACO
which will be operating under the twosided model to repay the Medicare
program in the case of incurred losses.
The following table provides a
summary comparison of the program’s
two models:
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a. Beneficiary Notification and
Protections
Because we believe participants in
risk models have an increased incentive
to lower costs, we also recognize there
may also be an increased incentive for
ACOs to avoid at-risk beneficiaries. We
believe that the monitoring procedures
that we are proposing as discussed in
section II.H. of this proposed rule, in
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combination with our proposed use of a
retrospective beneficiary assignment
methodology and proposed beneficiary
notification requirements, are sufficient
to guard against the prospects that twosided model ACOs might try to avoid atrisk beneficiaries in order to minimize
the possibilities of realizing losses
against their benchmarks. However, we
invite comments on the sufficiency of
these proposed monitoring procedures
as well as additional areas and
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mechanisms for monitoring two-sided
model ACOs.
b. Eligibility Requirements
We believe the eligibility
requirements for ACOs we are
proposing for the one-sided model, as
discussed in section II.B. of this
proposed rule, in combination with the
proposed requirement that ACOs
entering the two-sided model receive
our approval of their repayment
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mechanisms, are sufficient to ensure the
ability of ACOs to pay CMS in the event
they incur losses. We invite comments
on whether additional eligibility
requirements are necessary for ensuring
that ACOs entering the two-sided model
would be capable of repaying us if
actual expenditures exceed their
benchmark.
c. Quality Performance Measurement
and Scoring
We believe that the comprehensive
quality performance standards that we
have proposed for the one-sided model
are also appropriate for the two-sided
model. However, it is worth
emphasizing in this context that we
place great importance on the quality
aspects of the Shared Savings Program,
and that the quality standards take on
even greater importance for ensuring
high quality of care for beneficiaries
since we are proposing to incorporate a
requirement that all ACOs participating
in the Shared Savings Program accept
risk either beginning in year 1 or year
3 of their initial agreement period.
Therefore, in order to provide greater
incentives for organizations to
participate under the two-sided model,
we are proposing higher shared savings
rates under the two-sided model.
Specifically, we are proposing a sharing
rate of up to 60 percent (based on
quality performance) under this model,
compared to a sharing rate of up to 50
percent under the one-sided model, as
discussed in section II.E. of this
proposed rule. We propose that each of
the 5 quality measure domains in Table
2 would continue to be equally
weighted. Thus, each domain would be
worth 12 percent of the savings
generated by the ACO. That is, 5
domains × 12 percent equals 60 percent
of the total savings generated by the
ACO. Under this model, high
performers in quality scoring would
continue to earn more than lower
quality performers. As discussed in
section II.E. of the proposed rule, Table
3 illustrates our proposed sliding scale
for determining points earned for each
measure; we are proposing that under
the two-sided model ACOs, like onesided model ACOs, could earn a
maximum of 2 points per measure.
As discussed in section II.E. of this
proposed rule, the quality performance
standard for the first year of the Shared
Savings Program will be set at full and
accurate reporting. For the purposes of
determining the shared savings rate for
Track 2 ACOs, ACOs which meet this
standard will obtain the maximum
savings rate for quality performance (60
percent). As previously proposed, under
Track 1, ACOs will be reconciled using
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the methodology under the one-sided
model for the first and second year of
the agreement. In the third year of the
ACO’s agreement under Track 1, the
methodology used to reconcile ACOs
under the first year of the two-sided
model would apply for payment
purposes. With respect to the quality
performance standard, Track 1 ACOs in
the third year of their agreement must
meet the quality performance standard
that applies in the third program year,
as opposed to the first year standard of
full and accurate reporting.
We considered a number of
alternatives to incorporating features
that mirror the quality performance
standard proposed for the one-sided
model into determining the shared
savings and shared losses under the
two-sided model. That is, as proposed,
under the two-sided model ACOs could
increase their share of savings or
decrease their amount of losses with
higher quality scores. Alternatives track
to the options considered for
establishing the quality performance
standard discussed in section II.E. of
this proposed rule. An alternative is to
take a threshold approach to measuring
quality performance for the purpose of
determining the amount of shared
savings or losses. A third option is to
use a blend of these two options, by
allowing ACOs to increase their share of
savings with higher quality scores but
use a threshold approach when
calculating losses, so that higher quality
does not reduce an ACO’s share of any
losses. We seek comment on these
alternate approaches.
d. Shared Savings Methodology
As discussed in Section II.F. of this
proposed rule, we are proposing that
ACOs choosing to participate in the onesided model could share savings if they
exceed a minimum savings rate (MSR).
For those ACOs whose savings exceed
the MSR in the one-sided model, we are
proposing a savings sharing rate of up
to 50 percent of total savings, above a
2 percent savings threshold, with a
payment cap of 7.5 percent of an ACO’s
benchmark. We are also proposing an
additional increase of up to 2.5
percentage points for including FQHCs
and/or RHCs as ACO participants, as
discussed in section II.F of this
proposed rule. Thus, under our
proposal, an ACO participating in the
one-sided model could realize a
maximum shared savings rate of 52.5
percent.
For purposes of the two-sided model,
we are proposing to adopt the same
methodology for determining shared
savings, with some changes and
incentives outlined below. In
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comparison to the one-sided model, the
ACOs participating in the two-sided
model would: (1) Have increased
incentive payments for the same quality
performance and including FQHCs and/
or RHCs as ACO participants; (2) would
be subject to a fixed minimum savings
rate and minimum loss rate of 2 percent
and would share in gross savings once
the MSR is exceeded; and (3) would be
responsible for a portion of the excess
expenditures above the benchmark
based on their quality performance and
inclusion of FQHCs and/or RHCs. ACOs
with excess expenditures within the
minimum loss rate would not be
responsible for repaying Medicare.
ACOs with expenditures exceeding the
minimum loss rate would be
responsible for paying excess
expenditures calculated by multiplying
the amount of excess above the
benchmark by one minus the final
sharing rate. The final sharing rate is
defined as the quality performance
sharing rate plus the percentage points
for including FQHCs and/or RHCs as
ACO participants. ACOs would be
responsible for paying the percentage of
excess expenditures up to the annual
loss cap which is measured as a
percentage of the benchmark: 5 percent,
7.5 percent and 10 percent respectively
across the first 3 years for Track 2 ACOs;
an ACO in Track 1 who has entered the
third year of its initial agreement period
would be liable for an amount not to
exceed the percentage of the first year of
the two-sided model, that is, it would
not exceed 5 percent.
(1) Minimum Savings Rate
We believe that the MSR remains
important under the two-sided model to
guard against normal variation in costs,
so that ACOs share savings or losses
with the program only under those
circumstances in which we can be
confident that such savings or losses are
the result of the ACO’s behavior rather
than normal variation. At the same time,
we believe that it is more appropriate to
employ a fixed minimum savings rate
under this model. First, the greater
predictability of a fixed minimum
savings rate is more likely to attract
organizations to participate under this
model. Second, greater protection to the
Medicare trust fund is afforded by ACOs
accepting the risk of paying Medicare
back for losses. Therefore, based on our
experience with the Physician Group
Practice demonstration and consistent
with the lowest applicable MSR under
the one-sided model, we are proposing
to adopt a fixed 2 percent MSR for
organizations operating under this
model, in place of the variable
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(2) Additional Shared Savings Payments
In the one-sided model described
previously in this proposed rule, we
propose to increase an ACO’s share in
savings for including FQHCs and/or
RHCs as ACO participants. To further
increase the ACO’s reward for taking
risk, we are proposing to double this
amount, awarding a sliding scale
increase of up to 5 percentage points for
including FQHCs and/or RHCs as ACO
participants in an ACO participating in
the two-sided model, compared to 2.5
percentage points available under the
one-sided model.
(3) Net Sharing Rate
As discussed in section II.F. of this
proposed rule, we considered several
options for the amount of savings an
ACO could receive under the one-sided
model. These options included
requiring the ACO to exceed the MSR
and then sharing either on a first dollar
basis or sharing with the ACO savings
in excess of a threshold amount. We
proposed that for the first 2 years of the
agreement for the one-sided model that
ACOs which exceed the MSR would be
eligible to share in savings net of a 2
percent threshold, calculated as 2
percent of their benchmark. We further
proposed that small ACOs under the
one-sided model which meet certain
criteria (namely, physician-driven
ACOs, rural ACOs, and ACOs caring for
underserved populations) which
generate savings that exceed the MSR
will be eligible to share in savings on a
first dollar basis.
We considered the same options on
limiting the amount of savings an ACO
could receive under the two-sided
model. A number of factors favored
allowing two-sided model ACOs to
share on first dollar savings. For one,
ACOs participating in the two-sided
model are assuming the risk of losses
due to normal year-to-year variations in
Medicare beneficiaries’ claims
expenditures. Second, sharing first
dollar savings with two-sided model
ACOs would provide greater reward for
ACOs that choose to participate in the
program’s two-sided model as compared
to the one-sided model. Therefore, we
propose that two-sided model ACOs
which generate savings that exceed the
MSR will be eligible to share in savings
on a first dollar basis. Thus, under the
two-sided model, the final sharing rate
(quality performance sharing rate and
any additional increases for including
FQHCs and/or RHCs) would be applied
to an ACO’s total savings that exceed its
benchmark.
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(4) Calculating Sharing in Losses
In addition to a methodology for
determining shared savings, the twosided model requires a methodology for
determining shared losses in those cases
where an ACO realizes a loss as
opposed to a savings against its
benchmark in any performance year. As
discussed previously, we considered
several options for calculating the
amount of shared losses, tracking the
options considered for establishing the
quality performance standard. While a
methodology for determining shared
losses is obviously not necessary under
a one-sided model, we have mirrored
the structure and features of the shared
savings methodology as much as
possible to the determination of loss
sharing. Thus, for purposes of the losssharing methodology, we propose
adopting a similar structure of
minimum loss rate (the equivalent of
minimum savings rate on the savings
side), shared loss cap, and adjustments
to the shared loss percentage based on
the ACO’s quality performance and
inclusion of FQHCs and/or RHCs.
As noted previously, we are
proposing a minimum loss rate for
purposes of computing shared losses
when an ACO’s actual expenditures
exceed its benchmark. As in the case of
shared savings, we believe that losses
must exceed some minimum percentage
around the benchmark in order to
provide sufficient confidence that the
losses experienced during a given
performance year are not simply the
result of random variation. Further, we
are also proposing a cap on the loss
sharing rate under the two-sided model,
as we discuss later in this proposed
rule.
In addition, as in the determination of
shared savings, we are proposing to
adjust the loss sharing rate by
considering several factors related to
performance and behavior. These factors
would include: (1) Performance on
quality measures; and (2) any additional
adjustment for including FQHCs and/or
RHCs as ACO participants. However, in
order to recognize these factors
appropriately in the determination of
the shared loss rate, these factors must
operate as decreases in the ACO’s
shared loss rate, rather than as the
increases that they represent in the
determination of the shared savings rate.
For example, a two-sided model ACO
that realizes savings against its
benchmark may qualify for a final
sharing rate of up to 65 percent if it is
eligible for the maximum adjustments.
In this case, the 65 percent final sharing
rate is comprised of the savings rate of
up to 60 percent for quality
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performance, plus 5 percentage points
for including FQHCs and/or RHCs as
ACO participants.
On the other hand, a two-sided model
ACO that experiences actual
expenditures in excess of its benchmark
may qualify for a shared loss rate as low
as 35 percent of total losses if it is
eligible for the maximum adjustments to
its shared loss rate. So, for example, if
the ACO obtained maximum points for
its quality performance, and also
received the maximum adjustment for
including FQHCs and/or RHCs as ACO
participants, it would have a sharing
rate of 65 percent for purposes of
sharing in savings. But since there are
losses, the quality performance and
inclusion of FQHCs and/or RHCs should
be taken into consideration when
calculating losses owed to the program.
Accordingly, under our proposed
methodology we would multiply the
total losses by 1 minus the 65 percent
final sharing rate, or 35 percent, making
the ACO responsible for only 35 percent
of the amount of losses.
As discussed in section II.E. of this
proposed rule, the quality performance
standard for the first year of the Shared
Savings Program will be set at full and
accurate reporting. Therefore, for the
purposes of determining the loss sharing
rate, two-sided model ACOs which meet
this standard will obtain the maximum
savings rate for quality performance (60
percent), making them responsible for
40 percent of any losses under the
methodology previously described,
absent any increases in the sharing rate
for FQHC/RHC participation.
(5) Maximum Shared Savings and
Shared Loss Caps
We are proposing a maximum shared
loss cap, so that the shared losses that
an ACO might be required to return to
the Medicare program under this model
could not exceed a designated
percentage of an ACO’s benchmark in
any performance year. However, in
order to provide a greater incentive for
organizations to participate in the
Shared Savings Program under the twosided model, we are proposing to phase
in this shared loss cap over a 3-year
period. Specifically, we are proposing a
shared loss cap of 5 percent of the
benchmark in the first year of the
Shared Savings Program, 7.5 percent in
the second year, and 10 percent in the
third year.
ACOs electing the one-sided model
that are transitioned to the two-sided
model in the third year of their
agreement would be subject to the 5
percent cap on losses since they would
be considered to be in their first year
under the two-sided model.
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beneficiaries is $8,000 the maximum
amount of losses an ACO would be
responsible for the first year is 5 percent
of its benchmark, 7.5 percent the second
year, and 10 percent the third year.
Therefore, the ACO’s maximum per
capita liability could range from $400 to
$800 per assigned beneficiary. Actual
liability depends on the ACO’s actual
final sharing rate which incorporates its
quality performance and any increases
for inclusion of FQHCs and/or RHCs.
Continuing this example, if an ACO
with a benchmark of $8,000 per capita
has actual costs for its assigned
beneficiaries of $8,800, it would have a
per capita loss of $800. The following
table presents how much of the loss the
ACO would be responsible to pay back
under the program based on its final
sharing rate, as determined by its
quality performance, and assuming no
additional increases for FQHC/RHC
participation.
(e) Ensuring ACO Repayment of Shared
Losses
Ensuring that ACOs entering the twosided model will be capable of repaying
us for costs that exceed their benchmark
is a critical program requirement.
Financial protection requirements for
other entities with which CMS does
business provide examples of potential
mechanisms for recouping payment. In
order to enroll in and bill the Medicare
program, some Durable Medical
Equipment, Prosthetics, Orthotics, and
Supplies (DMEPOS) suppliers are
required to obtain a surety bond. Home
Health Agencies (HHA) entering into the
Medicare program must have available
sufficient ‘‘initial reserve operating
funds’’ at the time of application
submission—and at all times during the
enrollment process up to the expiration
of the 3-month period following the
conveyance of Medicare billing
privileges. CMS, through an
intermediary, determines the amount of
the HHA’s required initial reserve
operating funds using reported cost and
visit data from submitted cost reports
for the first full year of operation from
at least three HHAs that the
intermediary serves that are comparable
to the HHA.
As discussed in section II.F. of this
proposed rule, we propose a flat 25
percent withholding rate will be applied
annually to an ACO’s earned
performance payment. We propose that
this withholding serve as a component
of the repayment mechanism ACOs will
need to establish to ensure their ability
to repay Medicare for incurred losses.
We propose that we would apply the
withheld amount towards repayment of
an ACO’s losses. However, we recognize
that the 25 percent withholding of
shared savings may be inadequate to
cover the total amount of shared losses,
particularly if a Track 2 ACO
experiences losses in its first year. In
order to more fully ensure that the
Medicare program is paid back in the
event that an ACO incurs losses, we
have considered a number of options,
including the following:
• Recoup funds from the ACO and
require the ACO to obtain reinsurance,
place ACO funds in escrow, obtain
surety bonds, or establish a line of credit
as evidenced by a letter of credit that the
Medicare program can draw upon.
• Recoup funds from an ACO via the
ACO’s participants. We would require
the ACO to disclose on its application
the percentage of shared losses that each
ACO participant would be responsible
for, and the ACO would provide copies
of signed agreements with its ACO
participants, establishing their liability.
We would require ACO participants to
agree to have their future Medicare
payments reduced by the amount
reflected in the agreement. We note that
such arrangements, to the extent they
involve remuneration between referral
sources and those seeking referrals, may
raise liability issues under the physician
self-referral law and anti-kickback
statute. CMS and the OIG have solicited
comments on how best to approach this
issue in the Medicare Program; Waiver
Designs in Connection with the
Medicare Shared Savings Program and
the Innovation Center, also released
today.
• Withhold an additional portion of
any annual shared savings payments (on
top of the proposed flat 25 percent
withhold discussed in section II.F. of
this proposed rule in order to guard
against losses in subsequent years. This
could be done in combination with
other alternatives in order to guard
against any losses incurred by ACOs
that have not previously received shared
savings sufficient to offset such losses.
• Permit ACOs to specify how they
would repay us, for example through
one or more of the previously noted
recoupment options.
We further considered requiring an
ACO to establish a self-executing
method of repaying losses, using one or
more of the aforementioned options, to
demonstrate its ability to repay a
prescribed portion of its possible losses.
Another option we considered was to
require ACOs to use only one of these
repayment mechanisms. In that regard,
we considered requiring ACOs to obtain
a letter of credit in an amount not less
than the maximum potential downside
exposure for the ACO in any given
performance year (for example 5 percent
of the benchmark in the first
performance year for an ACO entering
Track 2, or for a Track 1 ACO entering
its third performance year of its initial
agreement period).
After considering these options, we
propose to require that an ACO establish
a self-executing method for repaying
losses to the Medicare program by
indicating that funds may be recouped
from Medicare payments to the ACO’s
participants, obtaining reinsurance,
placing funds in escrow, obtaining
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Additionally, as discussed previously,
we are proposing a higher maximum
shared savings cap under the two-sided
model, so that shared savings payment
under this model could not exceed 10
percent of an ACO’s benchmark,
compared to 7.5 percent under the onesided model.
An example of estimating an ACO’s
maximum potential downside risk and
estimating the ACO’s yearly losses is as
follows. If the ACO’s annual average per
capita benchmark for assigned
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surety bonds, establishing a line of
credit as evidenced by a letter of credit
that the Medicare program can draw
upon, or establishing another repayment
mechanism, such as those previously
discussed. This proposal assures
operational simplicity without
establishing eligibility requirements that
might discourage ACOs with limited
risk-bearing experience from entering
Track 2.
We considered several options for
determining the adequacy of an ACO’s
recoupment mechanism. One option
would be to require ACOs to
demonstrate an ability to repay the
maximum amount of possible losses, for
example 5 percent of the benchmark in
the first performance year for an ACO
entering Track 2, or for a Track 1 ACO
entering its third performance year of its
initial agreement period. Such a
requirement could be prohibitively
burdensome given that ACOs may need
to demonstrate their ability to repay a
large amount of capital and potentially
excessive given that ACOs’ loss rates
would be reduced to account for quality
performance and inclusion of FQHCs
and/or RHCs and ACOs have a limited
probability of incurring the maximum
possible losses. Another option,
potentially equally as effective as the
first but less onerous, would be to
require ACOs to demonstrate their
ability to repay losses, defined as a
percentage of the benchmark but below
the annual loss cap. Either option would
require the ACO to estimate anticipated
losses, and for CMS to confirm this
amount against the ACO’s benchmark
(once available). Given the anticipated
variation in ACO composition and
regional variations in cost, there may be
numerous ways of accurately estimating
an ACO’s maximum potential downside
risk. We further recognize that an ACO’s
assigned number of beneficiaries may
vary from year to year. Given the
potential for fluctuation in the size of an
ACO’s assigned population, and the
increase in the cap on shared losses in
the second and third years under Track
2, the sufficiency of the ACO’s
repayment mechanism would need to be
periodically reassessed to ensure its
adequacy.
We propose that an ACO must
demonstrate having established a
repayment mechanism, using one or
more of the recoupment methods
proposed previously, sufficient to
ensure repayment of losses equal to at
least 1 percent of per capita
expenditures for its assigned
beneficiaries from the most recent year
available. We further propose that we
will determine the adequacy of an
ACO’s repayment mechanism prior to
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its entrance into a period of
participation in the Shared Savings
Program. We also propose that an ACO
must demonstrate the adequacy of this
repayment mechanism annually, prior
to the start of each performance year in
which it takes risk, to ensure that it is
adequate to cover the anticipated
number of assigned Medicare
beneficiaries. An ACO must maintain
this repayment mechanism, ensuring
adequate capitalization of funds in the
case of some recoupment methods (such
as adequately funded escrow accounts
or reinsurance coverage), for the
duration of the performance year and up
until the time when we would need to
be reimbursed for the ACO’s losses. We
would ensure that an ACO maintains an
adequate repayment mechanism
through monitoring activities. We invite
comments on this proposal and on the
other options we have considered, as
well as alternate suggestions for
assuring risk-bearing ACOs have an
appropriate amount of available funds
to repay potential losses.
We further propose that an ACO
would be required, as part of its
application, to submit documentation of
such a repayment mechanism for
approval by us. This documentation
would include details supporting the
adequacy of the mechanism for repaying
the ACO’s maximum potential
downside risk exposure. An ACO
applying for Track 2 would be required
to submit this documentation as part of
its initial application. An ACO applying
for Track 1 would also be required to
submit this documentation as part of its
Shared Savings Program application
since Track 1 ACOs will be required to
transition to the two-sided model in the
third year. We believe it is important
that ACOs electing Track 1 can
demonstrate that they can fulfill the
requirements for the full three year
agreement period and that we do not
create an incentive for ACOs to
terminate their agreements prior to the
start of the third year under Track 1. As
a result, it is important to ensure that
prior to entry into the Shared Savings
Program, the ACO has an appropriate
plan for how it will repay any losses
incurred during the third year of its
agreement when it is automatically
transitioned to the two-sided model.
To the extent that an ACO’s
repayment mechanism does not enable
us to fully recoup the losses for a given
performance year, we propose to carry
forward unpaid losses into subsequent
performance years (to be recouped
either against additional financial
reserves, or by offsetting shared savings
earned by the ACO). We invite
comments on this proposal and on other
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options that we have considered, as well
as alternate suggestions for assuring that
any losses by ACOs participating in the
two-sided model can be recouped, the
processes for recouping losses from
these ACOs and/or their ACO
participants, and the appropriate
amount of available funds a risk-bearing
ACO should be required to have.
(f) Future Participation of UnderPerforming Organizations
As discussed in section II.C. of this
proposed rule, we propose that an ACO
which experiences a net loss during its
first 3-year agreement period may not
reapply to participate in the Shared
Savings Program because it has been
unsuccessful in lowering the growth in
Medicare expenditures and/or its
activities contributed in increases in
Medicare expenditure growth. We
believe this proposal is a means for
ensuring that under-performing
organizations do not continue to
increase Medicare expenditure growth.
We seek comment on this proposal and
whether denying continued
participation in the Shared Savings
Program for ACOs that under-perform
would create disincentives for the
formation of ACOs. We are specifically
interested in whether this requirement
will create disincentives for
participation among smaller ACOs.
(g) Public Reporting
We believe that the public reporting
requirements proposed under the onesided model should also apply to the
two-sided model. One such proposed
requirement is for ACOs to report
publicly on the shared savings received
by ACOs. Given that the purpose of this
proposed requirement is to enhance
transparency of the program we further
propose that ACOs under the two-sided
model publicly report on their amount
of losses, if any. We invite comments on
this proposed public reporting
requirement and whether, for the
purpose of ensuring transparency, there
is any additional information that
would be important for two-sided model
ACOs to publicly report.
(h) Impact on States
Finally, we emphasize that, under our
proposal for a two-sided model under
the Shared Savings Program, the
Medicare program retains the insurance
risk and responsibility for paying claims
for the services furnished to Medicare
beneficiaries, and that the agreement to
share risk against the benchmark would
be solely between the Medicare program
and the ACO. We do not intend that any
of our proposals concerning the Shared
Savings Program would render States
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responsible for bearing any costs
resulting from the operation of this
program. However, we note that each
State has its own insurance and risk
oversight programs and that some States
may regulate risk bearing entities, such
as the ACOs participating in the twosided model under the Shared Savings
Program. Accordingly, we seek
comment on whether any of our
proposals for the two-sided model in
particular, or the Shared Savings
Program in general, would trigger the
application of any State insurance laws,
the adequacy of those provisions that
we have set forth, and the ways that we
can work with ACOs and States to
minimize the burden of any additional
regulation.
4. Verification of Savings and Losses
We will notify an ACO in writing
regarding whether the ACO qualifies for
a shared savings payment, and if so, the
amount of the payment due. Similarly,
we will provide written notification to
an ACO of the amount of shared losses,
if any, that it must pay to the program.
We propose that an ACO must make
payment in full to CMS of any shared
losses within 30 days of receipt of
notification. Because we will calculate
amounts due to, or owed by, the ACO
on the basis of information submitted by
the ACO, we propose that the ACO must
certify the accuracy, completeness, and
truthfulness of such information. We
propose that, as a condition of receiving
a shared savings payment, the ACO
must submit to us a written request for
the shared savings payment amount.
The written request must certify the
ACO’s compliance with program
requirements for the relevant
performance period as well as the
accuracy, completeness, and
truthfulness of any information
submitted to us by the ACO, or its ACO
participants, or the ACO providers/
suppliers, or another entity, including
the accuracy, completeness, and
truthfulness of TINs used to assign
patients, any quality data or other
information or data relied upon by us in
determining the ACO’s eligibility for,
and the amount of, the shared savings
payment. In the case of an ACO
participating in the two-sided model
that has incurred shared losses, we
propose to require submission of a
similar certification at such time that
would provide us with assurance of the
ACO’s compliance with program
requirements for the relevant
performance period and the accuracy,
completeness, and truthfulness of any
data or other information submitted by
the ACO upon which we rely in
calculating the amount of shared losses.
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H. Monitoring and Termination of ACOs
Section 1899(d)(3) of the Act, as
added by section 3022 of the Affordable
Care Act, authorizes the Secretary to
‘‘impose an appropriate sanction’’ on an
ACO, including ‘‘termination from the
program,’’ if the Secretary determines an
ACO ‘‘has taken steps to avoid patients
at risk in order to reduce the likelihood
of increasing costs to the ACO.’’ We
discuss later in the document our
proposal to monitor ACOs for avoidance
of at-risk beneficiaries and to take
appropriate corrective actions when
ACOs are found to have engaged in this
prohibited conduct, including
termination where necessary.
Section 1899(d)(4) of the Act
authorizes the Secretary to terminate an
agreement with an ACO that does not
meet the established quality
performance standards. As discussed
later in the document, we propose to
monitor ACO performance with respect
to our proposed quality standards.
Subsequently, we discuss our proposal
to terminate ACOs that fail to meet
quality performance standards which
are described in section II.E. of this
proposed rule.
Section 1899 of the Act sets forth a
number of requirements for ACOs, and
authorizes the Secretary to promulgate
additional criteria that ACOs must
satisfy in order to be eligible to
participate in the Shared Savings
Program. The statute does not prescribe
procedures for monitoring nor what
factors we should consider in imposing
sanctions against an ACO, including
termination of its 3-year agreement for
reasons beyond avoiding patients at risk
and not meeting established quality
standards. Based on our experience with
other Medicare programs, as discussed
this proposed rule, we believe it is
important for patient protection and to
effectuate the Shared Savings Program
that we monitor an ACO to determine if
it meets additional Shared Savings
Program requirements not set forth in
section 1899 of the Act and take actions
such as termination with ACOs that are
not in compliance with additional
Shared Savings Program requirements
that are not set forth in section 1899 of
the Act. We discuss our proposal to
monitor ACO performance with respect
to these requirements and to terminate
or otherwise sanction ACOs that are not
in compliance with the requirements of
the Shared Savings Program.
In implementing other Medicare
programs, including the MA and the
Medicare Prescription Drug programs,
we have gained extensive experience in
monitoring organizational, provider,
and supplier behavior with respect to
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compliance with Medicare program and
program integrity requirements, quality
measurement, and avoidance of
particular types of beneficiaries. For
purposes of the Shared Savings
Program, we propose to employ many of
the methods we have developed for
purposes of the MA and Medicare
prescription drug programs to monitor
and assess ACOs and their participating
providers and suppliers. In general, the
methods we could use to monitor ACO
performance may include, but are not
limited to the following:
• Analysis of specific financial and
quality data as well as aggregated
annual and quarterly reports.
• Site visits.
• Assessment and following up
investigation of beneficiary and
provider complaints.
• Audits (including, for example,
analysis of claims, chart review,
beneficiary surveys, coding audits).
If based upon the monitoring
activities described previously we
conclude that an ACO’s performance
may subject the ACO to termination
from the Shared Savings Program, we
are proposing that CMS in its sole
discretion, may take any or all of the
following actions prior to termination of
the ACO from the Shared Savings
Program:
• Provide a warning notice to the
ACO of the specific performance at
issue.
• Request a corrective action plan
(CAP) from the ACO.
• Place the ACO on a special
monitoring plan.
We are seeking comment on additional
actions that may be appropriate prior to
termination.
A number of factors may trigger
heightened oversight of ACOs by us,
including conditions specified as the
bases for terminating the agreement
described in this proposed rule. Further,
we anticipate close examination of
ACOs that incur large losses to the
Medicare program.
In order to ensure that we have the
information necessary to conduct
appropriate monitoring and oversight of
ACOs, it will be necessary for ACOs,
ACO participants, and ACO providers/
suppliers, and other contracted entities
performing services and functions on
behalf of the ACO to retain records of
their activities under the Shared Savings
Program for a sufficient period of time
to allow the government to conduct the
appropriate audits, evaluations, and
inspections of their activities. A
‘‘contracted entity performing services
or functions on behalf of the ACO’’
would include any party that enters into
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an arrangement with an ACO to provide
services (including administrative,
management, or clinical services) to the
ACO or health care services to the
beneficiaries assigned to the ACO. It
also includes any party that enters into
an arrangement with an entity is in an
arrangement with the ACO down to the
level of the ultimate provider of
services.
We are proposing that an ACO, ACO
participant, ACO providers/suppliers,
and contracted entities performing
services and functions on behalf of the
ACO, will be required to maintain and
give us, the Department of Health and
Human Services (DHHS), the
Comptroller General, the Federal
Government or their designees, the right
to inspect all books, contracts, records,
documents, and other evidence
(including data related to Medicare
utilization and costs, quality
performance measures, shared savings
distributions, and other financial
arrangements related to ACO activities)
sufficient to enable the audit,
evaluation, and inspection of the ACO’s
compliance with Shared Savings
Program requirements and the ACO’s
right to any shared savings payment. We
propose that such books, contracts,
records, documents, and other evidence
be maintained by the ACO for a period
of 10 years from the end of the
agreement period or from the date of
completion of any audit, evaluation, or
inspection, whichever is later, unless
we determine there is a special need to
retain a particular record or group of
records for a longer period and notify
the ACO organization at least 30 days
before the normal disposition date. If
there has been a termination, dispute, or
allegation of fraud or similar fault by the
ACO organization or its members, we
propose that the retention may be
extended to 6 years from the date of any
resulting final resolution of the
termination, dispute, fraud, or similar
fault. We further propose that if we
determine that there is a reasonable
possibility of fraud or similar fault, we
may inspect, evaluate, and audit the
ACO organization at any time. If as a
result of any inspection, evaluation, or
audit, we determine that the amount of
shared savings due to the ACO or the
amount of shared losses owed by the
ACO has been determined in error, we
reserve the right to reopen the initial
determination and issue a revised initial
determination.
We further propose that ACOs include
terms in their agreements with ACO
participants, ACO providers/suppliers,
and the ACO and contracted entities
performing services and functions on
behalf of the ACO requiring them to
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comply with the same record retention
requirements and to make such books,
contracts, records, documents, and other
evidence available to the government
upon request. Notwithstanding any
arrangements between or among an
ACO, ACO participants, ACO providers/
suppliers, and contracted entities
performing services and functions on
behalf of the ACO, the ACO shall have
ultimate responsibility for adhering to
and otherwise fully complying with all
terms and conditions of its agreement
with CMS, including the record
retention requirement.
1. Monitoring Avoidance of At-Risk
Beneficiaries
As noted previously, section
1899(d)(3) of the Act authorizes the
Secretary to ‘‘impose an appropriate
sanction’’ on an ACO, including
‘‘termination from the program,’’ if the
Secretary determines an ACO ‘‘has taken
steps to avoid patients at risk in order
to reduce the likelihood of increasing
costs to the ACO.’’ While the statute
does not define what constitutes
‘‘patients at-risk’’, we believe such
patients are those beneficiaries who
have a high risk score on the CMS–HCC
risk adjustment model, are considered
high cost due to having two or more
hospitalizations or emergency room
visits each year, are dually eligible for
Medicare and Medicaid, have a high
utilization pattern, have one or more
chronic conditions (such as, for
example, diabetes, heart failure,
coronary artery disease, chronic
obstructive pulmonary disease,
depression, dementia, end stage renal
disease) or beneficiaries who have a
recent diagnosis (for example, newly
diagnosed cancer) that is expected to
result in an increased cost.
Such beneficiaries might be
appropriately targeted by an ACO to
implement care improvement strategies
to coordinate their care more efficiently.
However, high-cost beneficiaries are
also potentially at-risk for inappropriate
avoidance by an ACO because the ACO
may believe that it will be more likely
to realize shared savings against its
benchmark costs if it can avoid having
higher-cost patients assigned to it
during a performance year. We seek
comment on this definition of ‘‘at-risk
beneficiary’’ and whether other
beneficiary characteristics should be
considered in determining whether a
beneficiary is ‘‘at-risk.’’
To identify ACOs that could be
avoiding at-risk beneficiaries, we
propose to use a combination of
methods that would begin with an
analysis of claims and examination of
other beneficiary-level documentation
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(for example, beneficiary satisfaction
surveys, medical record audits,
beneficiary and provider complaints) to
identify trends and patterns suggestive
of avoidance of at-risk beneficiaries. The
results of these analyses could lead to
further investigation and follow-up with
the beneficiary or the ACO (including
ACO participants and ACO providers/
suppliers) in order to determine
whether avoidance of at-risk
beneficiaries has occurred. If as a result
of our analysis we conclude that an
ACO has been avoiding at-risk
beneficiaries during a performance year,
we propose to notify the ACO of our
determination and to require the ACO to
submit a corrective action plan (CAP)
for our approval. The CAP must address
actions the ACO will take to ensure that
the ACO, ACO participants, and ACO
providers/suppliers cease avoidance of
at-risk beneficiaries and must be
implemented as approved. In addition,
we propose that the ACO will be reevaluated both during and at the end of
the CAP. If we determine that the ACO
has continued to avoid at-risk
beneficiaries, the ACO would be
terminated from the Shared Savings
Program. We also propose that the ACO
would not receive shared savings
payments while it is under the CAP
regardless of the period of performance
in question and that the ACO would not
be eligible to earn any shared savings for
the period during which it is under the
CAP for avoiding at-risk beneficiaries.
We solicit comments on whether
lesser sanctions may be appropriate
when an ACO avoids at-risk
beneficiaries, such as the cessation of, or
a reduction in, the assignment of new
beneficiaries to the ACO, a reduction in
the amount of the shared savings
payment, or a fine for each instance of
at-risk beneficiary avoidance.
2. Monitoring Compliance With Quality
Performance Standards
Section 1899(d)(4) of the Act further
authorizes the Secretary to terminate an
agreement with an ACO that does not
meet the established quality
performance standards. To identify
ACOs that are not meeting the quality
performance standards, we will review
the ACO’s submission of quality
measurement data. We may request
additional documentation from an ACO
or its ACO participants or ACO
providers/supplier, as appropriate. In
those instances where an ACO fails to
meet the minimum attainment level for
one or more domains, we propose to
give the ACO a warning and to reevaluate the following year. If the ACO
continues to underperform on the
quality performance standards in the
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following year, the agreement will be
terminated. We also propose that if an
ACO fails to report one or more
measures, we would send the ACO a
written request to submit the required
data by a specified date and to provide
a reasonable written explanation for its
delay in reporting the required
information. If the ACO fails to report
by the requested deadline and does not
provide a reasonable explanation for
delayed reporting, we would
immediately terminate the ACO for
failing to report quality measures. We
further propose that ACOs that exhibit
a pattern of inaccurate or incomplete
reporting or fail to make timely
corrections following notice to resubmit
may be terminated from the program.
We note that since meeting the quality
standard is a condition for sharing in
savings, the ACO would be disqualified
from sharing in savings in each year in
which it underperforms.
3. Terminating an ACO Agreement
There are a number of important
program requirements that ACOs must
satisfy in order to be eligible to
participate in the Shared Savings
Program. As a result, in addition to the
statutory provisions at section
1899(d)(3) and (d)(4) of the Act
regarding termination for avoidance of
at-risk beneficiaries and for failure to
meet the quality standards, we believe
the agreement with an ACO should be
contingent upon that ACO continuing to
meet the requirements for eligibility to
participate in the Shared Savings
Program. Accordingly, we propose that
an ACO’s failure to continue to meet the
eligibility requirements for participation
in the Shared Savings Program should
also result in an ACO’s termination from
the Shared Savings Program. As
described in section II.F. of this
proposed rule, termination of an ACO
from the Shared Savings Program by us
or at the ACOs request for any reason
will result in loss of the mandatory 25
percent withhold of shared savings.
Therefore, we are proposing that
based upon monitoring and assessing
ACO operations (including ACO
participants and ACO providers/
suppliers), we may terminate an
agreement with an ACO before the end
of the 3-year agreement period for any
of the following reasons:
• Avoidance of at-risk beneficiaries as
described previously.
• Failure to meet the Shared Savings
Program’s quality performance standard
as described previously.
• Any material change impacting
ability to meet eligibility requirements,
including but not limited to the
following:
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++ Changes in ACO participants that
are the basis for beneficiary assignment.
++ Increase in ACO provider/
supplier composition that results in a
reviewing Antitrust Agency to state it is
likely to challenge or recommend
challenging the ACO.
++ Changes in the ACO’s leadership
and management structure that result in
an inability to perform the functions
discussed in section II.B. of this
proposed rule.
++ Sanctions or other actions taken
against the ACO, its ACO participants,
and ACO providers/suppliers, or
contracted entities performing services
or functions on behalf of the ACO, by
an accrediting organization, or by a
State, Federal or local government
agency.
• Failure of the ACO to effectuate
required regulatory changes during the
agreement period after given the
opportunity for a CAP.
• Failure of an ACO to demonstrate
that it has adequate resources in place
to repay losses and to maintain those
resources for the agreement period.
• Noncompliance with requirements
regarding beneficiary notification of
provider/supplier participation in an
ACO.
• Failure to completely and
accurately report or failure to make
timely corrections.
• Material noncompliance, or a
pattern of noncompliance, with public
reporting and other CMS reporting
requirements.
• Limiting or restricting internally
compiled beneficiary summary of care
or medical records from providers and
suppliers both within and outside of the
ACO, to the extent permitted by law (for
example, not sharing beneficiary
medical records with providers or
suppliers not participating in the ACO
from whom the beneficiary chooses to
receive care).
• Failure to offer beneficiaries the
option to opt out of sharing claims
information.
• Improper use or disclosure of
claims information received from us in
violation of the HIPAA Privacy Rule,
Medicare Part D Data Rule, Privacy Act,
the data use agreement, or other
applicable laws or regulations.
• Violation of physician self-referral
prohibition, civil monetary penalty
laws, anti-kickback statute, other
antifraud laws, antitrust laws, or other
applicable Medicare laws, rules, or
regulations that are relevant to ACO
operations.
• Submission to us of false,
inaccurate, or incomplete data and or
information, including but not limited
to, information provided in the Shared
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Savings Program application, quality
data, financial data, and information
regarding the distribution of shared
savings.
• Failure to submit payment due to us
in a timely manner.
• Use of marketing materials or
activities or other beneficiary
communications subject to approval
that have not been approved by us as
discussed in section II.B.11.of this
proposed rule.
Furthermore, we believe it is
appropriate that an ACO should provide
notice if it elects to terminate its
participation in the Shared Savings
Program. Accordingly, we are proposing
to require an ACO to provide us with a
60-day notice if it chooses to terminate
its agreement. The ACO would be
required to notify us of its decision to
terminate its participation in the Shared
Savings Program and would also be
required to notify all of its ACO
participants and ACO providers/
suppliers, who would in turn be
required to notify beneficiaries in a
timely manner of the ACO’s decision to
withdraw from the Shared Savings
Program. As described in section II.F.of
this proposed rule, the ACO would
forfeit its mandatory 25 percent
withhold of shared savings.
Finally, we propose that an ACO that
has been terminated from the Shared
Savings Program may apply to
participate in the Shared Savings
Program again at the end of the original
3-year agreement period. To be eligible
to participate in the Shared Savings
Program, the ACO must demonstrate in
its application that it has corrected the
deficiencies that caused it to be
terminated from the Shared Savings
Program and has processes in place to
ensure that it will remain in compliance
with the terms of the new participation
agreement. We have proposed in section
II.G. of this proposed rule, that ACOs
may only have one agreement period
involving the one-sided model, thus
ACOs with corrected deficiencies that
wish to reenter the program only have
the option to do so under the two-sided
model.
For violations that we consider minor
in nature and pose no immediate risk or
harm to beneficiaries or impact on care,
we propose to allow ACOs the
opportunity to submit a corrective
action plan (CAP) before termination.
We further propose that the ACO must
submit a CAP for our approval by the
deadline indicated on the notice of
violation. The CAP must address what
actions the ACO will take to ensure that
the ACO, ACO participants, ACO
providers/suppliers, and entities
performing services or functions on
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behalf of the ACO will correct any
deficiencies to remain in compliance
with Shared Savings Program
requirements. The CAP must be
implemented as approved. The ACO’s
performance will be monitored during
the CAP process. Failure of the ACO to
submit, obtain approval for, or
implement a CAP may result in
termination of the agreement. Failure of
the ACO to demonstrate improved
performance upon completion of the
CAP may result in termination. We seek
comments on our proposal, including
any additional conditions that could
merit the termination of an ACO
agreement.
4. Reconsideration Review Process
Section 1899(g) of the Act, as added
by section 3022 of the Affordable Care
Act, states that there shall be no
administrative or judicial review of the
following actions:
• Specification of criteria for meeting
quality performance standards under
section 1899(a)(1)(B) of the Act.
• Assessment of quality of care
furnished by an ACO and the
establishment of quality performance
standards under section 1899(b)(3) of
the Act.
• Assignment of Medicare FFS
beneficiaries to an ACO under section
1899(c) of the Act.
• Determination of whether an ACO
is eligible for shared savings under
section 1899(d)(2) of the Act), the
amount of shared savings, including the
determination of the estimated average
per capita Medicare expenditures under
the ACO for Medicare FFS beneficiaries
assigned to the ACO and the average
benchmark for the ACO under section
1899(d)(1)(B) of the Act.
• Percent of shared savings specified
by the Secretary under section
1899(d)(2) of the Act and any limit on
the total amount of shared savings.
• Termination of an ACO under
section 1899(d)(4) of the Act for failure
to meet quality performance standards.
The statute is otherwise silent
regarding an ACO’s right to contest
decisions on such matters as eligibility
to participate in the Shared Savings
Program or termination for avoidance of
at-risk beneficiaries. Accordingly, we
believe it is important to establish a fair
administrative process by which ACOs
may request review of decisions, such as
the denial of an ACO application or the
termination of an existing ACO
agreement for reasons other than those
exempted by statute. An administrative
reconsideration process provides an
opportunity to resolve disputes quickly
and efficiently, and creates an
administrative record that can serve as
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the basis for any further review of the
agency’s decision.
Based on our experiences with the
Medicare durable medical equipment
prosthetics orthotics and supplies
(DMEPOS) competitive bidding program
and the MA Part C and D programs, we
are proposing to implement
reconsideration review procedure
similar to the review process used by
those programs for initial
determinations that are not precluded
from administrative or judicial review
by statute. These initial determinations
would include the denial of an ACO
application or the termination of an
ACO participation agreement. Under
this proposal, if we deny a Shared
Savings Program application, the
applicant would be able to request
reconsideration of our determination
from a CMS reconsideration official.
This process would not apply to
applicants who are rejected on the
grounds that their certified application
was not submitted by the required
deadline, because in this situation no
valid application would have been
submitted. In the case where an ACO
has entered a 3-year agreement and
subsequently met criteria for
termination, we will give the ACO
notification of our initial determination
to terminate the agreement. The ACO
would be able to request an
independent review from a CMS
reconsideration official who will
reconsider the initial determination.
We propose that if an ACO or ACO
applicant wants to request a review by
a CMS reconsideration official of an
adverse initial determination, it must
submit a written request by an
authorized official for receipt by CMS
within 15 days of the adverse initial
determination. If the 15th day is a
weekend or a Federal holiday, then the
timeframe is extended until the end of
the next business day. Failure to submit
a request for a reconsideration review
within 15 days will result in denial of
the request for a review.
Reconsideration reviews are
scheduled at the discretion of the
review official and may be held orally
(that is, in person, by telephone or other
electronic means) or on the record
(review submitted documentation). The
ACO or ACO applicant will receive
acknowledgement of the reconsideration
request that will outline the review
procedures. The burden of proof would
be on the ACO or ACO applicant to
demonstrate to the reconsideration
official with convincing evidence that
the termination or application denial is
not consistent with CMS’ regulations or
statutory authority. The ACO or ACO
applicant may not use the
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reconsideration process to submit
required documentation as evidence for
the record that was not previously
submitted to CMS by the applicable
deadline. Furthermore, the
reconsideration official will only
consider evidence for the record that is
submitted in the required format and in
the timeframes indicated in the
acknowledgement notification, unless
additional information is requested by
the official. Following the review, the
reconsideration official will issue a
recommended decision.
We further propose that if the ACO or
ACO applicant disagrees with the
recommendation of the reconsideration
official, it will have an opportunity to
request a record review of the initial
determination and recommendation of
the reconsideration official by an
independent CMS official who was not
involved in the initial determination or
the reconsideration review process. An
ACO or ACO applicant that wishes to
request an on the record review of the
reconsideration official’s
recommendation must submit an
explanation of why it disagrees with the
recommendation in the timeframe and
in the format indicated in the
recommendation letter. The CMS
official may also review the
recommendation of the reconsideration
official on his or her own motion. The
on the record review process will be
based only on evidence presented for
the reconsideration review. The CMS
official will review the recommendation
of the reconsideration official and the
supporting materials and make a final
agency determination.
If an ACO applicant requests a review
of a decision to deny its application,
and our initial determination is upheld,
the application will be considered to
have been denied based on the effective
date of the original notice of denial. An
ACO that requests a reconsideration
review of an initial determination to
terminate its participation in the Shared
Savings Program will be permitted to
continue to participate during the
review process. However, if our initial
determination to terminate the
agreement with the ACO is upheld, the
decision to terminate the agreement is
effective as of the date indicated in the
initial notice of termination.
An ACO whose Shared Savings
Program application has been denied or
whose Shared Savings Program
agreement has been terminated due to a
determination made by a reviewing
antitrust agency may not contest the
merits of the antitrust agency’s
determination through the
reconsideration review process
proposed in this rule. Furthermore, the
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reconsideration review process
proposed in this rule shall not be
construed to negate, diminish, or
otherwise alter the applicability of
existing laws, rules, and regulations or
determinations made by other
government agencies.
We invite public comment, in general,
on the structures and procedure of an
appropriate review process for ACOs
terminated for avoidance of at-risk
beneficiaries or other reasons not
exempted from review by statute.
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I. Coordination With Other Agencies
As mentioned previously, in
developing the Shared Savings Program,
and in response to stakeholder
concerns, we have worked very closely
with agencies across the Federal
Government to facilitate participation in
the Shared Savings Program and to
ensure a coordinated and aligned interand intra-agency effort in the
implementation of the program. The
result of this effort is the release of three
documents with which potential
participants are strongly encouraged to
become familiar. These documents
include: (1) A joint CMS and DHHS
Office of Inspector General (OIG)
Medicare Program; Waiver Designs in
Connection with the Medicare Shared
Savings Program and the Innovation
Center addressing proposed waivers of
the civil monetary penalties (CMP) law,
Federal anti-kickback statute, and the
physician self-referral law; (2) an
Internal Revenue Service (IRS) notice
soliciting comments regarding the need
for additional tax guidance for taxexempt organizations, including taxexempt hospitals, participating in the
Shared Savings Program; (3) a proposed
Antitrust Policy Statement issued by the
FTC and DOJ (collectively, the Antitrust
Agencies). In addition, we are proposing
to preserve the benefits of competition
for Medicare beneficiaries by precluding
newly formed ACOs with market power
from participating in the Shared Savings
Program.
1. Waivers of CMP, Anti-Kickback, and
Physician Self-Referral Laws
Certain arrangements between and
among ACOs, ACO participants, other
owners, ACO providers/suppliers, and
third parties may implicate the CMP law
(section 1128A(b)(1) and (2) of the Act),
the Federal anti-kickback statute
(section 1128B(b)(1) and (2) of the Act),
and/or the physician self-referral
prohibition (section 1877 of the Act).
Section 1899(f) of the Act authorizes the
Secretary to waive certain fraud and
abuse laws as necessary to carry out the
provisions of the Shared Savings
Program. Accordingly, pursuant to
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section 1899(f) of the Act, CMS and OIG
have jointly published elsewhere in this
Federal Register a Medicare Program,
Waiver Designs in Connection with the
Medicare Shared Savings Program and
the Innovation Center, which describes
and solicits public input regarding
possible waivers of the application of
certain CMP law provisions, the Federal
anti-kickback statute, and the physician
self-referral law to specified financial
arrangements involving ACOs under the
Shared Savings Program. In addition,
section 1115A(d)(1) of the Act, as added
by section 3021 of the Affordable Care
Act, authorizes the Secretary to waive
the same fraud and abuse laws, among
others, as necessary solely for the
purposes of carrying out the provisions
of section 1115A of the Act with respect
to the testing of certain innovative
payment and service delivery models by
the Innovation Center. The notice with
comment period published elsewhere in
this Federal Register also solicits public
input regarding that separate waiver
authority.
We expect that the waivers applicable
to ACOs participating in the Shared
Savings Program will be issued
concurrently with our publication of the
Shared Savings Program final rule. The
requirements of the Shared Savings
Program final rule will bear on the
scope of any waivers granted for the
Shared Savings Program. Because of the
close nexus between the final
regulations governing the structure and
operation of ACOs under the Shared
Savings Program and the development
of waivers necessary to carry out the
provisions of the Shared Savings
Program, CMS and OIG may, when
crafting waivers applicable to the
Shared Savings Program, consider
comments submitted in response to this
Shared Savings Program proposed rule
and the provisions of the Shared
Savings Program final rule. Conversely,
we may consider comments received in
response to the joint notice with
comment period when drafting the
Shared Savings Program final rule.
Members of the public submitting
comment on this proposed regulation
should consider commenting on the
proposed waivers, as well.
2. IRS Guidance Relating to Tax-Exempt
Organizations
Nonprofit hospitals and other health
care organizations recognized by the IRS
as tax-exempt organizations are likely to
participate in the development and
operation of ACOs in the Shared
Savings Program. Accordingly, the IRS
intends to solicit public comment on
whether existing guidance relating to
the Internal Revenue Code provisions
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governing tax exempt organizations is
sufficient for those tax-exempt
organizations planning to participate in
the Shared Savings Program through
ACOs, and if not, what additional
guidance is needed. The IRS also
intends to solicit comments concerning
what guidance, if any, is necessary for
tax-exempt organizations participating
in ACOs that conduct activities
unrelated to the Shared Savings
Program.
We plan to continue to work with the
IRS to ensure a coordinated and aligned
interagency effort in the implementation
of the program. Nothing in this
proposed rule should be construed to
modify, impair, or supersede the
applicability of any of the Federal tax
laws. For further guidance, tax-exempt
organizations and ACOs should review
the IRS notice and solicitation of public
comment.
3. Antitrust Policy Statement
Concurrently with the issuance of this
Shared Savings Program proposed rule,
the Antitrust Agencies have issued a
proposed Statement of Antitrust
Enforcement Policy Regarding
Accountable Care Organizations
Participating in the Medicare Shared
Savings Program (Antitrust Policy
Statement). The Antitrust Policy
Statement applies to collaborations
among otherwise independent providers
and provider groups formed after March
23, 2010 that have otherwise been
approved to participate, or seek to
participate, as ACOs in the Shared
Savings Program.
The Antitrust Policy Statement sets
forth an antitrust ‘‘Safety Zone’’ for
certain ACOs. Specifically, the Antitrust
Policy Statement provides that the
Antitrust Agencies, absent extraordinary
circumstances, will not challenge an
ACO that otherwise meets the CMS
criteria to participate in the Shared
Savings Program if ACO participants
that provide the same service (common
service) have a combined share of 30
percent or less of each common service
in each ACO participant’s Primary
Service Area (PSA), wherever two or
more ACO participants provide that
service to patients from that PSA. Also,
under the Rural Exception set forth in
the Antitrust Policy Statement, ACOs
may qualify for the Safety Zone under
certain circumstances even if their
combined PSA share for common
services would be greater than 30
percent. The Antitrust Policy Statement
further provides that an ACO outside
the Safety Zone may proceed without
scrutiny by the Antitrust Agencies if its
combined PSA share for each common
service, wherever two or more ACO
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antitrust laws. For further guidance,
ACOs should review the Antitrust
Policy Statement.
4. Prohibition Against Shared Savings
Program Participation by ACOs With
Market Power
a. Coordinating the Shared Savings
Program Application With the Antitrust
Agencies
In light of the Antitrust Agency Policy
Statement, we propose to require that,
except for an ACO that qualifies for the
rural exception articulated in the Policy
Statement, an ACO with a PSA share
above 50 percent for any common
service that two or more ACO
participants provide to patients from the
same PSA must submit to us, as part of
its Shared Savings Program application,
a letter from the reviewing Antitrust
Agency confirming that it has no
present intent to challenge or
recommend challenging, the proposed
ACO. Absent such a letter, the proposed
ACO will not be eligible to participate
in the Shared Savings Program. In
addition, the Antitrust Policy Statement
explains that ACOs that are outside the
Safety Zone and below the 50 percent
mandatory review threshold frequently
may be procompetitive. It highlights
how ACOs in this category that do not
impede the functioning of a competitive
market and that engage in
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procompetitive activities will not raise
competitive concerns and may proceed
without Agency scrutiny. However, to
provide additional antitrust guidance,
the Antitrust Policy Statement identifies
five types of conduct that an ACO can
avoid to significantly reduce the
likelihood of an antitrust investigation.
An ACO in this category that desires
further certainty regarding the
application of the antitrust laws to its
formation and planned operation also
can seek an expedited review from the
Antitrust Agencies, similar to the
mandatory review described previously.
Such an ACO will not be eligible to
participate in the Shared Savings
Program if the reviewing Antitrust
Agency reviews the ACO and
determines that it is likely to challenge
or recommend challenging the ACO as
anticompetitive. Finally, we propose
that an ACO that falls within the Safety
Zone would not be required to obtain an
Antitrust Agency review as a condition
of participation. As noted in the
Antitrust Policy Statement, the Antitrust
Agencies are committed to providing
expedited reviews for ACOs that exceed
the 50 percent threshold and for those
ACOs that fall below the 50 percent
threshold and seek greater antitrust
certainty. The procedures for obtaining
such review are set forth in the Antitrust
Policy Statement.
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participants provide that service to
patients from that PSA, is less than or
equal to 50 percent. An ACO in this
category is also highly unlikely to
present competitive concerns if it avoids
certain specified conduct. The Antitrust
Policy Statement explains, however,
that for ACOs that do not meet the Rural
Exception, a combined PSA share for
common services of more than 50
percent provides a valuable indication
of an ACO’s potential for competitive
harm.
The Antitrust Policy Statement
outlines a methodology by which ACOs
can calculate their shares of common
services (that is, the same services
provided by two or more ACO
participants) provided to patients from
the same PSA. The common services
consist of physician specialties, major
diagnostic categories (‘‘MDCs’’) for
inpatient settings, and outpatient
categories for outpatient settings. We
will make public the information
necessary to designate common services
and to calculate the pertinent PSA
shares.
We plan to continue to work with the
Antitrust Agencies to determine the
extent to which additional action may
be appropriate with regard to ACOs in
the Shared Savings Program. Nothing in
this proposed rule should be construed
to modify, impair, or supersede the
applicability of any of the Federal
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Additionally, we recognize there may
be instances during the 3-year
agreement period where there is a
material change (as discussed in section
II. C.) in the participant and/or
provider/supplier composition of an
ACO. When this occurs, we have
proposed that the ACO must notify us
of the change within 30 days and that
the ACO must recalculate and report at
that time their PSA shares for common
services that two or more independent
ACO participants provide to patients
from the same PSA. We propose that if
any revised PSA share is calculated to
be greater than 50 percent, the ACO will
be subject to mandatory review or rereview by the Antitrust Agencies in
order to maintain the benefits of
competition for Medicare beneficiaries
and eligibility to participate in the
Shared Savings Program. Finally, we
propose that if the ACO fails to obtain
a letter from the reviewing Antitrust
Agency confirming that it has no
present intent to challenge or
recommend challenging the ACO, the
ACO will be terminated from the Shared
Savings Program.
The purpose of requiring Antitrust
Agency confirmation that it has no
present intent to challenge or
recommend challenging the ACO as a
condition of participation is two-fold.
First, the proposal ensures that ACOs
participating in the Shared Savings
Program will not present competitive
problems that could subject them to
antitrust challenge that may prevent
them from completing the term of their
3-year agreement with us. Section
1899(b)(2)(B) of the Act provides that
ACOs shall enter into an agreement with
the Secretary to participate in the
program for not less than a 3-year
period. We believe the requirement that
ACOs be willing and able to commit to
a 3-year agreement to participate in the
Shared Savings Program is necessary to
ensure that the program achieves its
long-term goal of redesigning health
care processes, and our proposal here
furthers that intent.
Second, the proposal maintains
competition for the benefit of Medicare
beneficiaries by reducing the potential
for the creation of ACOs with market
power. As discussed in more detail later
in the document, we believe that
competition in the marketplace benefits
Medicare and the Shared Savings
Program because it promotes quality of
care for Medicare beneficiaries and
protects beneficiary access to a variety
of providers. Furthermore, competition
benefits the Shared Savings Program by
allowing the opportunity for the
formation of two or more ACOs in an
area, which could accelerate
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advancements in quality and efficiency.
All of these benefits to Medicare
patients would be reduced or eliminated
if we allow ACOs to participate in the
Shared Savings Program when their
participation would create market
power.
b. Competition and Quality of Care
Because Medicare prices are
regulated, ACOs participating in the
Shared Savings Program will not
compete on the basis of price.
Nevertheless, economic theory and
competition policy suggest that these
ACOs will compete to serve Medicare
beneficiaries on the basis of nonprice
dimensions such as quality of care,
innovations that improve care, and
choice in treatment options. Empirical
studies of the Medicare program
confirm this theory and demonstrate
that, where prices are fixed, competition
among health care providers produces
higher quality for consumers.22 The
most prominent study of markets with
fixed prices examined the impact of
market concentration on mortality for
Medicare heart attack patients. The
study found that mortality was
significantly higher for patients in more
concentrated markets.23 A later study
had similar findings in that high-risk
Medicare patients’ heart attack mortality
was higher in highly concentrated
markets, while there was no such effect
for low-risk patients.24 Overall, the
evidence suggests that competition in
the presence of regulated prices fosters
improved quality.
The means by which competition
fosters improvements in quality,
innovation, and choice for Medicare
patients can vary. For example,
competition among ACOs can:
• Motivate innovation in the use of
existing treatment and care protocols
and the development of new protocols.
ACOs with better quality would be
expected to attract more patients, and
ACOs with both better quality and lower
costs would obtain a greater percentage
of shared savings.
22 See Daniel P. Kessler & Mark B. McClellan, Is
Hospital Competition Socially Wasteful? 115
Quarterly Journal of Econ. 577 (2000); Daniel P.
Kessler & Jeffrey J. Geppert, The Effects of
Competition on Variation in the Quality and Cost
of Medical Care, 14 Journal of Econ. and Mgmt.
Strategy 575 (2005). See also Abigail Tay Assessing
Competition in Hospital Care Markets: The
Importance of Accounting for Quality
Differentiation 34 RAND Journal of Econ. 786
(2003).
23 Daniel P. Kessler & Mark B. McClellan, Is
Hospital Competition Socially Wasteful? 115
Quarterly Journal of Econ., 577 (2000).
24 Daniel P. Kessler & Jeffrey J. Geppert, The
Effects of Competition on Variation in the Quality
and Cost of Medical Care 14 Journal of Econ. and
Mgmt. Strategy, 575 (2005).
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• Accelerate the development of
evidence-based best practices. In some
instances, physicians may differ on the
best course of treatment in a given case.
In the early stages of developing
evidence-based best practices, there may
be no way to know which practice or
care protocols among several
alternatives would be most effective. An
ACO with market power may have less
incentive to test alternative practices or
care protocols.
• Raise the likelihood of preserving
alternatives in the market, ultimately
leading to the emergency of better
procedures and treatments.
• Provide better benchmarks for
quality improvements. For example,
although a single ACO might claim that
environmental or demographic factors
limit what it can achieve in the
treatment of certain illnesses, a
comparison among multiple ACOs in
the same service area could better
ensure that the best standards possible
under prevailing conditions are being
met.
c. Competition, Price, and Access To
Care
A concern with potential ACO market
power in the commercial (as well as the
Medicare) market is warranted, because
recent commentary suggests that health
care providers are more likely to create
ACOs under the Shared Savings
Program if they can use the same ACOs
to serve both Medicare beneficiaries and
patients covered by commercial
insurance.25 If we permitted the creation
of ACOs with market power to operate
in the Shared Savings Program, those
ACOs would likely operate in the
commercial market as well. In the
commercial market, however, prices are
not regulated, so newly created ACOs
with market power could raise prices to
private purchasers and payers of health
care insurance above competitive levels.
Higher commercial prices create
disparities in payment rates between
commercial purchasers and payers
compared to Medicare rates. As reported
in a study by MedPAC staff, hospitals
with high payments from private payers
had high levels of overall profitability.26
Similarly, ACOs may wish to increase
the profitable private patients they serve
and, as a result, reduce the number of
25 Federal Trade Commision & Department of
Health and Human Services, Medicare Program;
Workshop Regarding Accountable Care
Organizations, and Implications Regarding
Antitrust, Physician Self-Referral, Anti-kickback,
and Civil Monetary Penalty (CMP) Laws, 75 FR
57039.
26 Report to Congress: Medicare Payment Policy,
111th Cong. (2010), available at https://
www.medpac.gov/documents/Mar10_Entire
Report.pdf.
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Medicare beneficiaries they serve. In
this way, commercial price increases
resulting from newly created ACOs with
market power could limit access to care
for Medicare beneficiaries. Our proposal
to require ACOs that exceed the 50
percent threshold to undergo a
mandatory antitrust review seeks to
ensure that there are sufficient providers
to allow the formation of competing
ACOs to serve Medicare beneficiaries.
In summary, we believe that it is
reasonable and appropriate to make
approval of an ACO’s Shared Savings
Program application and continuation
in the program contingent on the
absence of a determination by the
reviewing Antitrust Agency that it is
likely to challenge or recommend
challenging the ACO, or in the case of
an ACO that exceeds the 50 percent
threshold, on the ACO’s submission of
written confirmation from the reviewing
Antitrust Agency that it has no present
intent to challenge or recommend
challenging the ACO.
We plan to continue to work with the
Antitrust Agencies to determine the
extent to which additional actions may
be appropriate with regard to ACOs
participating in the Shared Savings
Program. We will also work closely with
the Innovation Center (which is charged
with considering whether the models it
tests demonstrate effective linkage with
other public and private sector payers)
and will use the results from the ACO
models it tests to inform possible future
rulemaking that may be necessary in
order to maintain ACO competition for
the benefit of Medicare beneficiaries.
Nothing in these regulations shall be
construed to modify, impair, or
supersede the applicability of the
antitrust laws.
srobinson on DSKHWCL6B1PROD with PROPOSALS2
J. Overlap With Other CMS Shared
Savings Initiatives
1. Duplication in Participation in
Medicare Shared Savings Programs
The statute includes a provision that
precludes duplication in participation
in shared savings programs. Section
1899 of the Act states that providers of
services or suppliers that participate in
certain programs are not eligible to
participate in the Shared Savings
Program. Section 1899(b)(4)(A) and (B)
of the statute, as added by section 3022
of the Affordable Care Act, states these
exclusions are ‘‘(A) a model tested or
expanded under section 1115A [the
Innovation Center] that involves shared
savings under this title or any other
program or demonstration project that
involves such shared savings; (B) the
independence at home medical practice
pilot program under section 1866E.’’
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Other shared savings programs that
include the opportunity for Medicareenrolled TINs to earn payment, in the
form of shared savings, for savings to
Medicare for Part A and B services
rendered to Medicare FFS beneficiaries
would be considered duplicative. We
have determined that the following
existing shared savings programs
overlap with the Shared Savings
Program and therefore, a Medicareenrolled TIN may not participate in both
the Shared Savings Program and one of
the following:
• Independence at Home Medical
Practice Demonstration program, as
established by section 3024 of the
Affordable Care Act.
• Medicare Health Care Quality
Demonstration Programs, as established
by section 646 of the Medicare
Modernization Act.
• Medical home demonstrations with
a shared savings element: Currently, the
only such Medicare demonstration that
includes a shared savings component is
the multi-payer advanced primary care
demonstration
• Physician Group Practice Transition
Demonstration.
Additional programs, demonstrations,
or models with a shared savings
component may be introduced in the
Medicare program in the future.
Interested parties should check the CMS
Web site for an updated list to ensure
that a provider or supplier participating
in the Shared Savings Program does not
participate in another Medicare program
or demonstarion involving shared
savings.
The prohibition against duplication in
participation in shared savings
programs applies only to programs that
involve shared savings under Medicare,
and the following are examples of such
programs established by the Affordable
Care Act which are unlikely to generate
duplicative shared savings:
• State initiatives to provide health
homes for Medicaid enrollees with
chronic conditions as authorized under
section 2703 of the Affordable Care Act.
• Program to establish community
health teams to support patient-centered
medical homes under section 3502 of
the Affordable Care Act.
We believe a principal reason
underlying the prohibition against
participation in multiple shared savings
programs is to prevent a provider or
supplier from being rewarded twice for
achieving savings in the cost of care
provided to the same beneficiary. As
discussed in section II.D. of this
proposed rule, we propose that
beneficiaries will be assigned to an ACO
based upon the TIN of the ACO
participant from which they receive the
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plurality of their primary care services.
Therefore, to ensure that a provider or
supplier is rewarded only once with
shared savings for the care of a
beneficiary, an ACO participant may not
also participate in another Medicare
program or demonstration involving
shared savings. However, in order to
maintain as much flexibility as possible
for ACO providers/suppliers to
participate concurrently in multiple
CMS shared savings programs, we do
not believe it is appropriate to extend
this prohibition to individual providers
and suppliers. We explore alternative
provider incentives, payment
arrangements and care delivery
mechanisms through its shared savings
programs, often specific to subsets of
Medicare or Medicaid beneficiaries. To
further our understanding of the
delivery of cost effective and high
quality care, and to ensure beneficiaries
receive the most appropriate care
possible relative to their needs,
individual practitioners should have the
opportunity to concurrently participate
in multiple shared savings programs.
Accordingly, an ACO provider/supplier
who submits claims under multiple
Medicare-enrolled TINs may participate
in both the Shared Savings Program and
another shared savings program if the
patient population is unique to each
program and if none of the relevant
Medicare-enrolled TINs participate in
both programs. For example, an ACO
practitioner participating in the Shared
Savings Program under an ACO
participant practice TIN could also
participate in the Independence at
Home Demonstration under a different
TIN that is not an ACO participant since
there would be no duplication in
beneficiary assignment; and therefore,
no duplication in shared savings.
We propose a process for ensuring
that savings associated with
beneficiaries assigned to an ACO
participating in the Shared Savings
Program are not duplicated by savings
earned in another Medicare program or
demonstration involving shared savings.
If such a program assigns beneficiaries
based upon the TINs of health care
providers from whom they receive care,
we will compare the participating TINs
in the program with those in the Shared
Savings Program to ensure that TINs
used for beneficiary assignment to an
ACO participating in the Shared Savings
Program are unique and that
beneficiaries are assigned to only one
shared savings program. If the other
program or demonstration involving
shared savings does not assign
beneficiaries based upon the TINs of the
health care providers from whom they
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srobinson on DSKHWCL6B1PROD with PROPOSALS2
receive care, but uses an alternate
beneficiary assignment methodology,
we propose working with the
developers of the respective
demonstrations and initiatives to devise
an appropriate method to ensure no
duplication in shared savings payment.
Applications for participation in the
Shared Savings Program that include
TINs that are already participating in
another Medicare shared savings
program will be rejected.
2. Transition of the Physician Group
Practice (PGP) Demonstration Sites Into
the Shared Savings Program
The PGP demonstration, authorized
under section 1866A of the Act, was our
first experience with a shared savings
program in Medicare. The PGP
demonstration serves as a model for
many aspects of the Shared Savings
Program. Section 1899(k) of the Act
speaks directly to the treatment of the
PGP demonstration. ‘‘During the period
beginning on the date of the enactment
of this section and ending on the date
the program is established, the Secretary
may enter into an agreement with an
ACO under the demonstration under
section 1866A of the Act, subject to
rebasing and other modifications
deemed appropriate by the Secretary.’’
As the final performance year of the
initial five year PGP demonstration
concluded in March 2010, this section
of the Affordable Care Act authorizes
the Secretary to extend the PGP
demonstration.
It is likely that the 10 physician
groups in the PGP demonstration will be
uniquely situated and qualified to be
among the organizations which are
ready to become early participants in
the Shared Savings Program. As noted
previously, consistent with section
1899(b)(4) of the Act, to be eligible to
participate in the Shared Savings
Program, a provider of services or
supplier may not also be participating in
a demonstration project that involves
shared savings, such as the PGP
demonstration. Thus, the PGP sites
would be permitted to participate in
either the PGP demonstration or the
Shared Savings Program under section
1899 of the Act, but could not
participate in both. Since assignment
methodologies are similar between the
Shared Savings Program and the PGP
demonstration, we will provide for
unique assignment of beneficiaries by
ensuring there is no overlap in
participating Medicare-enrolled TINs as
mentioned previously.
We believe it is appropriate to
consider what transition process should
be available for those PGP
demonstration sites that wish to
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participate in the Shared Savings
Program. We do not believe that
automatically transferring the PGP
demonstration sites into the Shared
Savings Program is appropriate because
we are concerned that some of the PGP
demonstration participants may be
incapable of meeting the Shared Savings
Program’s requirements, thereby
jeopardizing the participant’s ability to
achieve the overall goals associated with
the Shared Savings Program, including
the ability to achieve shared savings. On
the other hand, requiring the PGP sites
to undergo the same application process
as all other entities would not account
for our familiarity with these
organizations, and their experience with
redesigning care processes and
improving quality in a shared savings
setting. In addition, requiring the sites
to undergo the full application process
could potentially deter qualified sites
that are currently participating in the
PGP demonstration from transitioning
from the PGP demonstration to the
Shared Savings Program.
We propose that should a PGP site
decide to apply for participation to the
Shared Savings Program, we will give
the site the opportunity to complete a
condensed application form. The
condensed application form would
require the applicant to provide the
information that is required for the
standard Shared Savings Program
application but that was not already
obtained through its application for or
via its participation in the PGP
demonstration and, if necessary, to
update any information contained in its
application for the PGP demonstration
that is also required on the standard
Shared Savings Program application.
For instance, the condensed application
would ensure that the PGP site satisfies
the eligibility requirements of the
Shared Savings Program, as follows:
• Establishing a shared governance
structure and leadership and
management structure according to
program requirements;
• Providing documentation around
processes for quality management and
patient engagement, and patientcenteredness criteria as described in
section II.B of this proposed rule.
However, it should be noted that some
PGP sites applying to the Shared
Savings Program may not constitute a
newly created ACO and therefore would
be exempt from the antitrust review
described previously in the
Coordination With Other Agencies
section of this preamble.
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3. Overlap With the Center for Medicare
& Medicaid Innovation (Innovation
Center) Shared Savings Models
Section 1899(i) of the Act gives the
Secretary the authority under the
Shared Savings Program to use other
payment models determined to be
appropriate, including partial capitation
and any additional payment model that
the Secretary determines will improve
the quality and efficiency of items and
services furnished under Medicare. The
purpose of the Innovation Center,
established in section 1115A of the Act,
as amended by section 3021 of the
Affordable Care Act, is to test innovative
payment and service delivery models to
reduce expenditures under Medicare,
Medicaid, and the CHIP, while
preserving or enhancing the quality of
care furnished to individuals under
these programs. Preparations are
currently underway to develop this
capability. Within the Innovation
Center, it may be possible to test
different payment models, provide
assistance to groups of providers and
suppliers that wish to develop into an
ACO, or enhance our understanding of
different benchmarking methods. As the
Innovation Center gains experience with
different ACO payment models, we can
use proven methods to enhance and
improve the Shared Savings Program
over time.
As mentioned previously, section
1899(b)(4) of the Act also restricts
providers of services and suppliers from
participating in both the Shared Savings
Program and other shared savings
programs and demonstrations. We
intend to coordinate our efforts to
ensure that there is no duplication of
participation in shared savings
programs through provider or supplier
participation in both the Shared Savings
Program and any shared savings models
tested by the Innovation Center.
Similarly, we will also take steps to
ensure there is a methodology to avoid
duplication of payments for
beneficiaries aligned with providers and
suppliers in both the Shared Savings
Program and any current or future
models tested by the Innovation Center.
Finally, the Innovation Center is
seeking input on how it can best test
different payment models that provide
financial and technical assistance to
groups of providers and suppliers that
may wish to develop into an ACO.
III. Collection of Information
Requirements
As stated in section 3022 of the
Affordable Care Act, Chapter 35 of title
44, United States Code, shall not apply
to the Shared Savings Program.
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Consequently, the information
collection requirements contained in
this proposed rule need not be reviewed
by the Office of Management and
Budget.
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.
srobinson on DSKHWCL6B1PROD with PROPOSALS2
V. Regulatory Impact Analysis
A. Introduction
We have examined the impacts of this
proposed rule as required by Executive
Order 12866 on Regulatory Planning
and Review (September 30, 1993),
Executive Order 13563 on Improving
Regulation and Regulatory Review
(January 18, 2011), the Regulatory
Flexibility Act (RFA) (September 19,
1980, Pub. L. 96–354), section 1102(b) of
the Act, section 202 of the Unfunded
Mandates Reform Act of 1995 (Pub. L.
104–4), Executive Order 13132 on
Federalism (August 4, 1999), and the
Congressional Review Act (5 U.S.C.
804(2)).
Executive Orders 12866 and 13563
direct agencies to assess all costs and
benefits of available regulatory
alternatives and, if regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety
effects, distributive impacts, and
equity). Executive Order 13563
emphasizes the importance of
quantifying both costs and benefits, of
reducing costs, of harmonizing rules,
and of promoting flexibility. This rule
has been designated an ‘‘economically’’
significant rule, under section 3(f)(1) of
Executive Order 12866. Accordingly,
the rule has been reviewed by the Office
of Management and Budget.
Section 202 of the Unfunded
Mandates Reform Act of 1995 (UMRA)
also requires that agencies assess
anticipated costs and benefits before
issuing any rule whose mandates
require spending in any 1 year of $100
million in 1995 dollars, updated
annually for inflation. In 2011, that
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threshold is approximately $136
million. This proposed rule does not
include any mandate that would result
in spending by State, local or tribal
governments, in the aggregate, or by the
private sector in the amount of $136
million in any one year. We
acknowledge that there will be costs
borne by the private sector, as discussed
in this regulatory impact section, in
order to participate in this program;
however, participation is voluntary and
is not mandated.
Executive Order 13132 establishes
certain requirements that an agency
must meet when it promulgates a
proposed rule (and subsequent final
rule) that imposes substantial direct
requirement costs on State and local
governments, pre-empts State law, or
otherwise has Federalism implications.
We do not believe that there is anything
in this proposed rule that either
explicitly or implicitly pre-empts any
State law, and furthermore we do not
believe that this proposed rule will have
a substantial direct effect on State or
local governments, preempt States law,
or otherwise have a Federalism
implication.
B. Statement of Need
This proposed rule is necessary to
implement section 3022 of the
Affordable Care Act which amended
Title XVIII of the Act (42 U.S.C. 1395 et
seq.) by adding a new section 1899 of
the Act to establish a Shared Savings
Program that promotes accountability
for a patient population, coordinates
items and services under parts A and B,
and encourages investment in
infrastructure and redesigned care
processes for high quality and efficient
service delivery. Section 1889(a)(1) of
the Act requires the Secretary to
establish this program not later than
January 1, 2012. Also, section
1889(a)(1)(A) of the Act states that
under this program, ‘‘groups of
providers of services and suppliers
meeting criteria specified by the
Secretary may work together to manage
and coordinate care for Medicare feefor-service beneficiaries through an
accountable care organization (referred
to as an ‘ACO’);’’ and section
1889(a)(1)(B) of the Act provides that
‘‘ACOs that meet quality performance
standards established by the Secretary
are eligible to receive payments for
shared savings * * *.’’
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The Shared Savings Program is a new
approach to the delivery of health care
aimed at reducing fragmentation,
improving population health, and
lowering overall health care costs.
The Shared Savings Program should
provide an entry point for all willing
organizations who wish to move in a
direction of providing value-driven
healthcare. Consequently, in accordance
with the authority granted to the
Secretary under sections 1899(d) and
1899(i) of the Act, we looked at creating
both a shared savings model (one-sided)
and a shared savings/losses model (twosided). The sharing parameters under
the two options are balanced so as to
provide greater reward for organizations
accepting risk while maintaining
sufficient incentive to encourage
providers to participate in the one-sided
model, providing an entry point to riskoriented models.
As detailed in Table 10, we estimate
a total aggregate median impact of $510
million in net Federal savings for CYs
2012 through 2014 from the
implementation of the Shared Savings
Program. (An estimate produced by the
Office of the Actuary on April 22, 2010
showed no net impact only because the
statute by itself lacked enough detail to
allow for scoring.) The 10th and 90th
percentiles of the estimate distribution,
for the same time period, show net
savings of $960 million and $170
million. These estimated impacts
represent the effect on Federal transfers.
The estimated aggregate cost for start-up
investment and first year operating
expenditures for ACOs in the Shared
Savings Program range from
$131,643,825 to $263,287,650, assuming
75 to 150 ACOs participating in the
Shared Savings Program. Furthermore,
the Shared Savings Program would
benefit beneficiaries since the program
requires ACOs to be accountable for
Medicare beneficiaries, improve the
coordination of FFS items and services,
encourage investment in infrastructure
and redesigned care processes for high
quality and efficient service delivery
that demonstrate a dedication and focus
toward patient-centered care.
Accordingly, we have prepared a RIA
that to the best of our ability presents
the costs and benefits of this proposed
rule. We solicit comment on the
assumptions and analysis presented
throughout this regulatory impact
section.
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As discussed in the preamble of this
proposed rule, the Shared Savings
Program establishes a program whereby
groups of suppliers and providers can
work together through ACOs that would
assume responsibility for managing and
coordinating the care of groups of
traditional FFS Medicare patients.
Participating ACOs will have the
opportunity to earn shared savings
payments by reducing Medicare
expenditure growth for their assigned
beneficiaries below specified target
thresholds or benchmarks while
simultaneously meeting quality
performance measures. An ACO could
initially opt for one of two program
tracks. The first option (one-sided
model) offers eligibility for shared
savings payments in years 1 and 2
without the risk of being responsible for
repaying any losses if actual
expenditures exceed the benchmark,
followed by a third year offering a
higher percentage of shared savings but
also risk for excess expenditures above
the benchmark. The second option (twosided model) provides an opportunity
for receiving a higher percentage of
shared savings for all 3 years, but with
potential liability in each of the 3 years
for annual expenditures that exceed the
benchmark.
There is substantial uncertainty as to
the number of ACOs that will
participate in the program, their
characteristics, provider and supplier
response to the financial incentives
offered by the program, and the ultimate
effectiveness of the changes in care
delivery that may result as ACOs work
to improve the quality and efficiency of
patient care. These program design and
other uncertainties complicate efforts to
assess the financial impacts of the
Shared Savings Program and result in a
wide range of potential outcomes
regarding the net impact on Medicare
expenditures.
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To best reflect these uncertainties, we
designed a stochastic model that
incorporates assumed probability
distributions for each of the key
variables that will affect the overall
financial impact of the Shared Savings
Program. Using a Monte Carlo
simulation approach, the model
randomly draws a set of specific values
for each variable, reflecting the expected
covariance among variables, and
calculates the program’s financial
impact based on the specific set of
assumptions. We repeated the process
for a total of 5,000 random trials,
tabulating the resulting individual cost
or savings estimates to produce a
distribution of potential outcomes that
reflects the assumed probability
distributions of the incorporated
variables, as shown in Table 10. In this
way, we can evaluate the full range of
potential outcomes based on all
combinations of the many factors that
will affect the financial impact, and
with an indication of the likelihood of
these outcomes. It is important to note
that these indications do not represent
formal statistical probabilities in the
usual sense, since basis for the
underlying assumptions for each of the
factors in the model are based on
reasonable judgments, using
independent expert opinion when
available.
The median result from the
distribution of simulated outcomes
represents the ‘‘best estimate’’ of the
financial effect of the Shared Savings
Program, recognizing the uncertainty
inherent in a new program with
uncertain responses. The full
distribution illustrates the uncertainty
surrounding the mean or median
financial impact from the simulation.
As detailed in Table 11, the median
estimate involves a combination of: (1)
Reduced actual Medicare expenditures
due to more efficient care; (2) shared
savings payments to ACOs; and (3)
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payments to CMS for shared losses
when actual expenditures exceed the
benchmark, resulting in a projected total
of $510 million in net savings over CYs
2012 through 2014. Approximately 97
percent of the stochastic trials resulted
in a net savings to the Medicare
program, while the other 3 percent
produced a net cost. At the extremes,
the greatest simulated savings was
approximately $1,960 million, while the
greatest simulated cost was $270
million.
A net savings (costs) occurs when the
payment of earned and unearned
shared-savings bonuses (less penalties
collected) resulting from— (1)
Reductions in spending; (2) program
design; and (3) random group claim
fluctuation, in total are less than (greater
than) assumed savings from reductions
in expenditures.
As we finalize the Shared Savings
Program provisions, and as the actual
number of participating ACOs and their
characteristics become known, the range
of financial outcomes will narrow.
Similarly, as data become available on
the initial differences between actual
expenditures and the target
expenditures reflected in ACO
benchmarks, it will be possible to
evaluate the financial effects with
greater certainty. The estimate
distribution shown provides an
objective and reasonable indication of
the likely range of financial outcomes,
given the chosen variables and their
assumed distributions at this time in the
program’s development.
C. Anticipated Effects
1. Effects on the Medicare Program
As a voluntary program involving an
innovative and complex mix of financial
incentives for quality of care and
efficiency gains within FFS Medicare,
the Shared Savings Program could result
in a wide range of possible outcomes.
While examples exist across the
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healthcare marketplace for risk-sharing
arrangements leading to efficiency
gains, a one-sided model would
presumably provide a weaker incentive
to ACOs than other possible approaches.
The optional two-sided risk model, and
the requirement for all other ACOs to
accept downside risk in their third
program year, both provide stronger
incentives than a shared savings only
approach. For example, under the onesided model, a provider’s worst-case
outcome is the failure to earn sharedsavings. A provider would operate
under the significant possibility that
there would be no impact on their
Medicare reimbursement. The two-sided
risk model, however, presents liability
for excessive expenditures, significantly
increasing a provider’s perceived
likelihood that aggregate Medicare
revenue will depend on the level of
efficiency with which they operate. In
addition, the two-sided model offers a
lower minimum savings rate and a
greater sharing percentage, both of
which enhance the incentive for
efficiency. However, participating ACOs
may be more likely to choose the onesided model for the first 2 years and
thereby avoid the potential for financial
loss if expenditures experience a
significant upward fluctuation or if
efficiency improvements are less
effective than planned.
In the third year of their first
agreement period, as noted previously,
all ACOs that participate in the onesided model during the first 2 years of
the agreement period will be required to
transition to the two-sided risk model.
We believe certain participating ACOs
may choose to terminate their agreement
early after the first 2 years. For example,
ACOs in Track 1 that failed to meet the
expenditure growth targets in the first 2
years (but were protected from penalties
by being in the one-sided model), would
likely reconsider their continuing
participation. Certain other ACOs, such
as those in higher-cost areas of the
country, could also terminate their
agreement if they anticipate that the
national growth formula, relative to
their local baseline cost, puts them in
jeopardy of experiencing losses in the
third year. (Under section 2899(d) of the
Act, we update ACO benchmarks by the
estimated annual increase in the
absolute amount of national average
Medicare Part A and Part B
expenditures, expressed as a flat dollar
amount for each year. As a result, the
updates to ACO benchmarks in
percentage terms will be higher in lowcost areas of the country and lower in
high-cost areas.) This scenario could
contribute to selective program
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participation by ACOs favored by the
national flat-dollar growth target.
While shared FFS savings, even with
optional liability for a portion of excess
expenditures, offers less incentive to
reduce costs or improve efficiency than,
say, full capitation, it still represents a
new incentive for efficiency. Sharedsavings (and potential liabilities) will
have varying degrees of influence on
hospitals, primary physicians, specialty
physicians, and other providers. The
expectation is for different ACOs to
comprise a varying mix of these
providers and suppliers. And while
certain care improvements might be
achieved relatively quickly (for
example, prevention of hospital
readmissions and emergency-room
visits for certain populations with
chronic conditions), many potential
ACOs might need more than 3 years to
achieve comprehensive efficiency gains.
Challenges include identification of
assigned beneficiaries, managing care
furnished by providers and suppliers
outside the ACO, lack of similar
contracts with other payers, achieving
buy-in from ACO providers and
suppliers, and the extent to which
possible future shared savings or losses
will affect the perceived value of
immediate FFS revenue for providers
and suppliers participating in the ACO.
a. Assumptions and Uncertainties
We sought input from a wide range of
external experts, including credentialed
actuaries, consultants, and academic
researchers, to identify the pertinent
variables that could determine the
efficacy of the program, and to identify
the reasonable ranges for each variable.
The assumptions identified and
stochastically modeled include the
following:
• Number of participating ACO
provider groups.
• Size mix of participating ACOs.
• Type of ACO that would consider
accepting risk under the two-sided risk
option.
• Participating ACOs’ current level of
integration and preparedness for
improving the quality and efficiency of
care delivery.
• Baseline per-capita costs for
prospective ACOs, relative to national
average.
• Number and profile of providers
and suppliers unavailable to participate
in the Shared Savings Program due to
participation in ACO models tested by
the Innovation Center.
• Range of savings for participating
ACOs within the first three years of the
program.
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• Local variation in expected claims
cost growth relative to the national
average.
• Quality reporting scores and
resulting attained sharing (or loss)
percentages.
Overall we assumed 1.5 to 4 million
Medicare beneficiaries would align with
a participating ACO during the first
three years of the program. We assumed
ACOs to be more likely to participate
from markets exhibiting baseline percapita FFS expenditures above the
national average. In addition, we
assumed the level of savings generated
by an ACO to positively correlate to the
achieved quality performance score and
resulting sharing percentage.
Of particular relevance is the high
degree of variability observed for local
per-capita cost growth rates relative to
the national average ‘‘flat dollar’’ growth
(used to update ACO benchmarks). The
benchmark or expenditure target
effectively serves as the only measure of
efficiency for participating ACOs.
Factors such as lower-than-average
baseline per-capita expenditure and
variation in local growth rates relative to
the national average can trigger Shared
Savings Program shared savings
payments even in the absence of any
efficiency gains. Similarly, some ACOs
could find that in the determination of
shared savings by factors such as
prevailing per-capita expenditure
growth in their service area that is
higher than the national average
overshadows their hard-fought
efficiency gains.
b. Detailed Stochastic Modeling Results
Table 11 shows the distribution of the
estimated net financial impact for the
5,000 stochastically generated trials.
(The amounts shown are in millions,
with negative net impacts representing
Medicare savings). The net impact is
defined as the total cost of shared
savings less—(1) any amount of savings
generated by reductions in actual
expenditures; and (2) any losses
collected for ACOs that accepted risk
and have actual expenditures exceeding
their benchmark.
The median estimate of the Shared
Savings Program financial impact for
calendar years 2012 through 2014 is a
net savings of $510 million. This
amount represents the ‘‘best estimate’’ of
the 3-year financial impact of the
Shared Savings Program initiative. It is
important to note, however, the
relatively wide range of possible
outcomes. Overall, 97 percent of the
stochastic trials resulted in net program
savings, and the other 3 percent
represented cost increases. The 10th and
90th percentiles of the estimated
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law, as it would be implemented
through this proposed rule. However,
OACT emphasizes the possibility of
outcomes that differ substantially from
the median estimate, as illustrated by
the estimate distribution. With the
adoption of final program provisions
and with additional data on the actual
number and characteristics of
participating ACOs, we can estimate the
financial impact with greater precision.
The projections assume the
assignment of roughly 1.5 to 4 million
beneficiaries to participating ACOs over
the first 3 years. To the extent that the
Shared Savings Program will result in
net savings or costs to Part B of
Medicare, revenues from Part B
beneficiary premiums would also be
correspondingly lower or higher. In
addition, because MA payment rates
depend on the level of spending within
traditional FFS Medicare, Shared
Savings Program savings or costs would
result in corresponding adjustments to
MA payment rates. Neither of these
secondary impacts has been included in
the analysis shown.
Table 12 shows the median estimated
financial effects for the Shared Savings
Program initiative, and the associated
10th and 90th percentile ranges, broken
out for each of the first 3 years. For the
first year, 2012, the median projection
indicates a $100 million savings,
primarily because the ACO costefficiency initiatives are generally not
assumed to have matured, but a number
of provider groups that benefit from
favorable random claim fluctuations or
from low baseline expenditure relative
to the national average would receive
shared saving payments. By the second
and third years, 2013 and 2014, of the
projection, the median estimates
indicate net savings of $210 million and
$200 million, respectively, from
increased cost-saving effectiveness
offset in part by shared savings paid due
to random variation and the (increasing)
variation in the accuracy of updated
national targets compared to actual local
growth as well as participation and
sharing percentage changes resulting
from mandatory transition to two-sided
risk in the third year. As a result, the
projections for years 2 and 3 cover a
wider range of possible outcomes,
reflecting a growing dependence on
uncertain assumptions for savings and
expenditure growth variation relative to
the national average.
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distribution show net savings of $960
million and $170 million, respectively,
suggesting a 10 percent likelihood that
the actual impact would fall outside
respective percentile amounts. In the
extreme scenarios, the results were as
large as $2 billion in savings or $270
million in costs.
Our Office of the Actuary (OACT)
prepared the stochastic model and
resulting financial estimates. OACT
believes that the median result of $510
million in savings is a reasonable ‘‘point
estimate’’ of the impact of the Shared
Savings Program provision in current
c. Further Consideration
The impact analysis shown is only for
the first 3-year agreement period.
Beyond this initial period, there is
additional uncertainty, in significant
part because the rules governing
subsequent Shared Savings Program
agreement periods have not yet been
developed. A risk exists that by ACOs
in low-cost areas could dominate the
Shared Savings Program, where
participation could be a relatively riskfree opportunity to achieve shared
savings simply due to the generous
benchmark presented by national
average ‘‘flat-dollar’’ growth. On the
other hand, the first 3-year agreement
period ACOs could foster significant
improvements in the quality and costefficiency of health care delivery,
leading to broader use of these
techniques nationwide and accelerated
adoption of risk-sharing arrangements
(such as partial capitation, bundled
payments, etc.). These changes could
result in significant efficiency gains in
FFS Medicare. The stochastic model for
the first 3 years of the program, does not
incorporate either of these longer-run
scenarios, but both remain
possibilities—subject to the final
program design and implementation. At
this time, an impact estimate expanded
to include performance beyond the
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initial 3-year period would likely entail
a significantly wider range of possible
outcomes. The results of the first
performance cycle, however, will help
inform estimates of the ongoing
financial effects of the Shared Savings
Program.
2. Impact on Beneficiaries
We anticipate the Shared Savings
Program will benefit beneficiaries
because the intent of the program is to
require ACOs to be accountable for
Medicare beneficiaries, improve the
coordination of FFS items and services,
encourage investment in infrastructure
and redesigned care processes for high
quality and efficient service delivery
that demonstrates a dedication and
focus toward patient-centered care.
Patient-centered care is a concept that
focuses healthcare delivery and
communication on the patient and those
who are close to the patient and bases
the care and communication delivered
around the needs of the beneficiary,
thus benefitting the beneficiary
community. This program does not
affect the beneficiary’s freedom of
choice regarding providers or care. Also,
a requirement of ACO participation in
the Shared Savings Program is reporting
of, and successful performance related
to, quality measures and patient-
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experience surveys. These aspects of the
Shared Savings Program will encourage
the provider and supplier community to
focus on and deliver improved quality
care. In addition to existing Medicare
monitoring programs that are in place to
protect beneficiaries, the Shared Savings
Program will include monitoring and
auditing processes to protect beneficiary
choice as well as ensure that
beneficiaries are receiving the
appropriate care. As is discussed in
more detail in the preamble, these
processes include monitoring ACO
avoidance of at-risk beneficiaries,
assessing and providing follow up on
beneficiary complaints, audits
(including, for example, analysis of
claims, chart review, beneficiary
surveys, coding audits) and analysis of
quality performance.
More specifically, we believe that
beneficiary impacts would be
maximized as the ACO meets the
mission of the Shared Savings Program,
as established by the Affordable Care
Act and embraces the following goals of
better health and experience of care for
individuals, better health for
populations and lower expenditure
growth. The ACO’s impact will be
demonstrated by how effectively it
delivers care as measured under the
financial methodology outlined in
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section II. F, Shared Savings
Determination, of this proposed rule,
how well it improves and delivers high
quality care outlined in the quality
measurement and reporting
methodology in section II.E. of this
proposed rule, and in meeting program
requirements for patient centered care
outlined in the eligibility section II.B. of
this proposed rule.
Therefore, because of the
accountability of ACOs for both the
quality and overall cost of care provided
to their assigned beneficiary population
and must meet the quality performance
standards prior to sharing any savings;
they have new incentives to improve the
health and well being of the
beneficiaries they treat. ACOs will
report on conditions and areas that are
high prevalence and high cost in the
Medicare population, such as chronic
disease, ambulatory care sensitive
conditions, care transitions and
readmissions, and patient experience.
We have observed that measuring
quality and providing incentives can
result in redesigned care processes that
provide clinicians with actionable
information on their patients at the
point of care which can lead to
improved patient care processes and
outcomes. For example, the Medicare
Physician Group Practice Demonstration
Fact Sheet (CMS, August 2009) showed
that over the first three years of the PGP
Demonstration, physician groups
increased their quality scores an average
of 10 percentage points on the 10
diabetes measures, 11 percentage points
on the ten congestive heart failure
measures, 6 percentage points on the
coronary artery disease measures, 10
percentage points on the cancer
screening measures, and 1 percentage
point on the hypertension measures.
Further analysis is provided in the
Physician Group Practice Demonstration
Evaluation Report (Report to Congress,
2009; https://www.cms.gov/
DemoProjectsEvalRpts/downloads/
PGP_RTC_Sept.pdf).
In addition to the overall increases in
quality scores, we can examine the
impact of the PGP Demonstration on
quality can be examined by comparing
the values of the seven claimsbased
quality measures for each PGP site and
its comparison group. Our analysis
found that, on the claims-based
measures, PGP performance exceeded
that of the comparison groups (CGs) on
all measures between the base year (BY)
and performance year 2 (PY2). It also
found that the PGP sites exhibited more
improvement than their CGs on all but
one measure between the BY and PY2.
Even after adjusting for predemonstration trends in the claims-
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based quality indicators, the PGP sites
improved their claims-based quality
process indicators more than their
comparison groups.
3. Impact on Providers and Suppliers
In order to participate in the program,
we realize that there will be costs borne
in building the organizational, financial
and legal infrastructure that is required
of an ACO as well as performing the
tasks required (as discussed throughout
the Preamble) of an eligible ACO, such
as: quality reporting, conducting patient
surveys and investment in infrastructure
for effective care coordination. While
provider and supplier participation in
the Shared Savings Program will be
voluntary, we have examined the
potential costs that program
participation will create.
The proposed rule allows for
flexibility regarding the specific
structure of an ACO and, as such, we
expect the costs to vary greatly.
Furthermore, beyond the statutorily
required assignment of at least 5,000
Medicare beneficiaries to an ACO, the
size of ACOs will also vary in relation
to beneficiary participation and
associated cost. Due to the limited
precedence for this program and
uncertainty regarding the structure and
strategies that the provider community
will pursue in order to participate as an
ACO, estimates of expected provider
costs are difficult to create. An analysis
produced by the Government
Accountability Office (GAO) of first year
total operating expenditures for
participants of the Medicare PGP
Demonstration varied greatly, from
$436,386 to $2,922,820, with the
average for a physician group at
$1,265,897 (Medicare Physician
Payment: Care Coordination Programs
Used in Demonstration Show Promise,
but Wider Use of Payment Approach
May Be Limited. GAO, February 2008).
These costs (for groups which all had
200 or more physicians) include
investments in infrastructure and
information technology enhancements,
management, quality reporting, and
focused care coordination programs.
The GAO also discovered that start-up
investment expenditures in the PGP
Demonstration varied between $82,573
and $917,398, with the average for a
physician group at $489,354.
It is worth noting that the 10
participating physician groups in the
demonstration were large compared
with other physician practices in terms
of annual medical revenues and
nonphysician staff. GAO claims that
their larger relative size gave the 10
participating physician groups in the
PGP Demonstration three size-related
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advantages over smaller physician
practices. First, participants typically
had institutional affiliations with an
integrated delivery system, a general
hospital, or a health insurance entity.
Specifically 9 of the 10 participating
physician groups were part of an
integrated delivery system, 8 affiliated
with a general hospital, and 5 affiliated
with an entity that marketed a health
insurance product. As a result of these
affiliations, GAO claims that
participating physician groups generally
had greater access to relatively large
amounts of financial capital needed to
initiate or expand programs. The second
advantage, GAO claims, the 10 large
participating physician groups had over
smaller physician practices is the
increased probability of having or
acquiring EHR systems, which was
essential in participants’ ability to
gather data and track progress in
meeting quality-of-care targets. For
example, 8 of the 10 participating
physician groups had an EHR in place
before the demonstration began, and the
2 other participants, out of necessity,
developed alternative methods for
gathering patient data electronically.
Lastly, GAO claims that the third sizerelated advantage that most of the 10
participating physician groups had over
smaller physician practices was the
larger groups’ experience with other
pay-for-performance systems prior to
participating in the PGP Demonstration.
That is, 8 of the 10 participants had
previous experience with pay-forperformance programs initiated by
private or public sector organizations.
This experience, GAO concludes, may
have eased their adjustment to the PGP
Demonstration and allowed them
greater initial and overall success.
We use this analysis not to predict
cost investment and operating
expenditures, but to demonstrate that
we expect the range of investment to
vary greatly across ACOs and to provide
potential scope for aspiring participants.
We expect that due to the difference in
program requirements between the
Shared Savings Program and the PGP
Demonstration Project, and the potential
variation in ACO size and structure, the
PGP related costs may be a subset of the
investment required by entities seeking
participation in this program. However,
we recognize that potential
advantageous key drivers for
participating physician groups would
include institutional affiliations that
allow greater access to financial capital,
access to and experience using EHR and
other IT systems and experience with
pay-for-performance programs. As a
result, we present a rough estimate of
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$1,755,251, based on the GAO findings
to reflect the total average start-up
investment and first year operating
expenditures for a participant in the
Shared Savings Program. Lastly,
assuming a range of expected ACOs
participating in the Shared Savings
Program at 75 to 150 yields an estimated
aggregate cost, for ACO start-up
investment and first year operating
expenditures in the Shared Savings
Program, in the range of $131,643,825 to
$263,287,650.
Participating in the Shared Savings
Program will require groups of
providers and suppliers to (among other
things): invest in or improve upon
information technology systems, focus
on evidence-based medicine, improve
care coordination and quality and
generally refine all processes of caring
for their patients and community.
While, as we discussed previously,
there will be a financial cost placed on
ACOs in order to do so, there will be
benefits to the respective organizations
in the form of increased operational and
healthcare delivery efficiency.
Furthermore, as discussed previously,
and explained in more detail in the
preamble of this proposed rule, there
will be an opportunity for financial
reward for success in the program in the
form of shared savings. The estimated
bonuses paid are a median of $800
million over 3 years, with $560 million
and $1,130 million reflecting the 10th
and 90th percentiles. Also, participating
ACO’s will be assuming a risk of a
financial penalty for failing to achieve
savings (that is, if actual expenditures
exceed the benchmark). The estimated
penalties paid are a median of $40
million over 3 years, with $10 million
and $80 million reflecting the 10th and
90th percentiles. (It is important to note
that the given percentiles for bonuses,
penalties, and net impacts are
independently tabulated and therefore
are not additive across the three
parameters.) The actuality of the risk is
dependent on which of the two options
an ACO selects for their first agreement
period. Due to the voluntary nature of
this program, we expect the formation of
ACOs by entities that aspire to receive
benefits that outweigh their costs. We
anticipate that not all ACOs will achieve
shared savings and some will incur a
financial loss, due to requirement to
repay a share of actual expenditures in
excess of their benchmark.
As is previously stated, we expect the
costs and benefits of establishing and
maintaining an ACO to vary and solicit
comment on this issue, including total
ACO expenditures for start-up
investment and annual operating costs
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for the 3 years of the Shared Savings
Program.
D. Alternatives Considered
The proposed rule contains a range of
policies. Many tenets of the program are
statutorily mandated and thus allow for
little, if any, flexibility in the
rulemaking process. Where there was
flexibility, we made our policy
decisions regarding alternatives based
on a balance between creating the least
possible negative impact on the
stakeholders affected by the program on
and satisfactorily fitting the vision of the
program within given operational
constraints.
For example, while the Affordable
Care Act mandates that an ACO be large
enough to care for minimum of 5,000
assigned beneficiaries, as is described in
the preamble, we are proposing a sliding
minimum percentage and confidence
interval for the savings threshold based
on the size of an ACO. This proposal is
a balance of protecting the program from
paying out savings based on random
variation, while allowing attainable
thresholds for smaller sized potential
ACOs and thus encouraging
participation from various sized entities.
The preceding preamble provides
descriptions of the various statutory
provisions that are addressed, identifies
those policies when discretion has been
allowed and exercised, presents the
rationales for our proposals and, where
relevant, alternatives that were
considered. An important example
involves adjustments to an ACO’s
benchmark for changes in FFS price
adjustments (such as the geographic
practice cost index (GPCI) under the
PFS and hospital wage index). Such
price changes regularly occur and often
impact counties or other localities in
magnitudes that can significantly differ
from the national average. If, for
example, operating cost payments are
reduced for section 508 hospitals (as
will occur under current law at the end
of FY 2011) then ACO-attributed claims
incurred in a 508 hospital would exhibit
significant price decreases which could
lead to shared savings payments
unrelated to real improvements in ACO
efficiency. Absent such adjustments,
these statutory changes will impact the
comparison of actual expenditures and
the benchmark. However, as we have
previously noted, the statute provides
authority for adjustment to the
benchmark for ‘‘such other factors as the
Secretary determines appropriate.’’
Another design element involves the
method for constructing a participating
ACO’s benchmark. One proposed
method employs a similar approach to
that used in the CMS PGP
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Demonstration and is based on riskadjusting to take into account changes
in the health status of the population
between the benchmark period and
performance year. If HCC risk
adjustments are specified in the final
program then it must be applied in a
manner that does not reward ACOs for
more complete and accurate coding of
their assigned patient population to
protect the program from costs due to
paying shared savings as a result of
greater diagnosis coding intensity in
ACOs than would occur for a
comparable group of beneficiaries
receiving care outside an ACO.
Finally, a key design element involves
the method for establishing quality
standards. We propose aggregating the
quality domain scores into a single
overall ACO score used to calculate the
ACOs final sharing rate for purposes of
determining shared savings or shared
losses as described in section II.E of this
proposed rule. We would average all
domain scores for an ACO together
equally to calculate the overall quality
score used to calculate the ACO’s final
sharing rate as previously described. We
also considered a variety of scoring
methodology that would have differing
incentives for improving clinical
outcomes such as: Scoring measures
individually under a method that would
weight all measures equally as well as
weighting quality measures by their
clinical importance. In addition to the
performance score approach that
rewards ACOs for better quality with
larger percentages of shared savings as
modeled in this analysis, we could use
a threshold approach that allows any
ACO that meets minimum standards for
the quality to realize the full shared
savings. By design this approach could
ensure higher net savings to the
Medicare program, depending on the
quality threshold and sharing
percentage chosen.
The provisions adopted in the final
Shared Savings Program rule may differ
from the current proposals, possibly
resulting in material changes in the
projected financial impact of the
program. We solicit comment on other
potentially effective and reasonably
feasible alternatives especially those
that reduce burdens and maintain
flexibility and freedom of choice for the
public.
E. Accounting Statement and Table
As required by OMB Circular A–4
(available at https://
www.whitehouse.gov/sites/default/files/
omb/assets/regulatory_matters_pdf/a4.pdf), in Table 13, we have prepared an
accounting statement showing the
classification of transfers, benefits and
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uncertainties identified in establishing
the economic impact estimates, we
intend to update the estimates in the
final rule.
F. Conclusion
As a result of this proposed rule, the
median estimate of the financial impact
from implementation of the Shared
Savings Program, for CYs 2012 through
2014, is a net savings of $510 million.
Although this is the ‘‘best estimate’’ for
the 3-year financial impact of the
Shared Savings Program initiative, a
relatively wide range of possible
outcomes exists. Overall, 80 percent of
the stochastic trials resulted in net
program savings, and the other 30
percent represented cost increases. The
10th and 90th percentiles of the
estimate distribution show net savings
of $960 million and $170 million,
respectively, suggesting a 10-percent
likelihood that the actual impact would
exceed the respective percentile
amounts. In the extreme scenarios, the
results were as large as $1,960 million
in savings or $270 million in costs.
Lastly, the estimated aggregate cost for
ACO start-up investment and first year
operating expenditures in the Shared
Savings Program range from
$131,643,825 to $263,287,650, based on
an assumed 75 to 150 ACOs
participating in the Shared Savings
Program.
In accordance with the provisions of
Executive Order 12866, this regulation
was reviewed by the Office of
Management and Budget.
Medicaid Services proposes to amend
42 CFR Chapter IV by adding part 425
to read as follows:
425.23 Public reporting and transparency.
425.24 Overlap with other CMS shared
savings initiatives.
SUBCHAPTER B—MEDICARE PROGRAM
Subpart A—General Provisions
PART 425—MEDICARE SHARED
SAVINGS PROGRAM
§ 425.2
List of Subjects in Part 425
Administrative practice and
procedure, Health facilities, Health
professions, Medicare, Reporting and
recordkeeping requirements.
For the reasons set forth in the
preamble, the Centers for Medicare &
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Subpart A—General Provisions
425.2 Basis and scope.
425.4 Definitions.
Subpart B—Shared Savings Program
Requirements
425.5 Eligibility and governance
requirements.
425.6 Assignment of Medicare fee-forservice beneficiaries to ACOs.
425.7 Payment and treatment of savings.
425.8 ACO quality and continuous
improvement goals.
425.9 Measures to assess the quality of care
furnished by an ACO.
425.10 Calculating the ACO quality
performance score and determining
shared savings eligibility.
425.11 Incorporating other reporting
requirements related to the Physician
Quality Reporting System and electronic
health records technology.
425.12 Monitoring.
425.13 Actions prior to termination.
425.14 Termination, suspension, and
repayment of Shared Savings.
425.15 Reconsideration review process.
425.16 Audits and record retention.
425.17 Requirements for data submission
by ACOs.
425.18 The 3-year agreement with CMS.
425.19 Data sharing with ACOs.
425.20 New program standards established
during the 3-year agreement period.
425.21 Managing significant changes to the
ACO during the agreement period.
425.22 Future participation of previous
Shared Savings Program participants.
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Basis and scope.
(a) Basis. This part implements
section 1899 of the Act by establishing
a shared savings program that promotes
accountability for a patient population,
coordinates items and services under
parts A and B, and encourages
investment in infrastructure and
redesigned care processes for high
quality and efficient services. Under this
program, groups of providers of services
and suppliers meeting criteria specified
by the Secretary may work together to
manage and coordinate care for
Medicare fee-for-service beneficiaries
through an accountable care
organization (ACO). ACOs that meet
quality performance standards
established by the Secretary are eligible
to receive payments for shared savings.
During years in which the ACO is
participating in a two-sided model, the
ACO may be required to share losses.
(b) Scope. This part sets forth the
following:
(1) The eligibility requirements for an
ACO to participate in the Medicare
Shared Savings Program (Shared
Savings Program).
(2) Program requirements, including
quality and other reporting
requirements.
(3) The method for assigning
Medicare fee-for-service beneficiaries to
ACOs.
(4) Payment criteria and
methodologies (one-sided model and
two-sided model).
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(5) Compliance monitoring and
sanctions for noncompliance.
(6) Reconsideration of adverse
determinations.
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§ 425.4
Definitions.
As used in this part, unless otherwise
indicated—
Accountable care organization (ACO)
means a legal entity that is recognized
and authorized under applicable State
law, as identified by a Taxpayer
Identification Number (TIN), and
comprised of an eligible group (as
defined at § 425.5(b)) of ACO
participants that work together to
manage and coordinate care for
Medicare fee-for-service beneficiaries
and have established a mechanism for
shared governance that provides all
ACO participants with an appropriate
proportionate control over the ACO’s
decision-making process.
ACO participant means a provider (as
defined in § 400.202) or a supplier (as
defined at § 400.202), as identified by a
TIN.
ACO provider/supplier means—
(1) A provider (as defined in
§ 400.202); or
(2) A supplier (as defined at
§ 400.202) that bills for items and
services it furnishes to Medicare
beneficiaries under a Medicare billing
number assigned to the TIN of an ACO
participant in accordance with
applicable Medicare rules and
regulations.
ACO professional means an ACO
provider/supplier who is either of the
following:
(1) A doctor of medicine or
osteopathy legally authorized to practice
medicine and surgery by the State in
which he performs such function or
action, including an osteopathic
practitioner within the scope of his or
her practice as defined by State law.
(2) A practitioner who is one of the
following:
(i) A physician assistant (as defined at
§ 410.74(a)(2)).
(ii) A nurse practitioner (as defined at
§ 410.75(b)).
(iii) A clinical nurse specialist (as
defined at § 410.76(b)).
Antitrust Agency means the
Department of Justice or Federal Trade
Commission.
Antitrust Policy Statement means the
Statement of Antitrust Enforcement
Policy Regarding Accountable Care
Organizations Participating in the
Medicare Shared Savings Program
issued by the antitrust agencies.
Assignment means the operational
process by which CMS determines
whether a beneficiary has chosen to
receive a sufficient level of the requisite
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primary care services from primary care
physician(s) who is an ACO provider/
supplier so that the ACO may be
appropriately designated as exercising
basic responsibility for that beneficiary’s
care.
At-risk beneficiary means a
beneficiary who—
(1) Has a high risk score on the CMS–
HCC risk adjustment model;
(2) Is considered high cost due to
having two or more hospitalizations
each year;
(3) Is dually eligible for Medicare and
Medicaid;
(4) Has a high utilization pattern; or
(5) Has had a recent diagnosis that is
expected to result in increased cost.
CAP means a corrective action plan.
Covered professional services has the
same meaning give these terms under
section 1848(k)(3) of the Act.
Eligible professional has the meanings
given this term under section 1848(k)(3)
of the Act.
Hospital means a hospital subject to
the prospective payment system
specified in § 412.1(a)(1) of this chapter.
Marketing materials and activities
include, but are not limited to, general
audience materials such as brochures,
advertisements, outreach events, letters
to beneficiaries, web pages, data sharing
opt out letters, mailings, or other
activities conducted by or on behalf of
the ACO, or by ACO participants, or
ACO providers/suppliers participating
in the ACO, or by other individuals on
behalf of the ACO or its participating
providers and suppliers when used to
educate, solicit, notify, or contact
Medicare beneficiaries or providers and
suppliers regarding the Shared Savings
Program. The following beneficiary
communications are not marketing
materials and activities: Informational
materials customized or limited to a
subset of beneficiaries; materials that do
not include information about the ACO
or providers in the ACO; materials that
cover beneficiary-specific billing and
claims issues or other specific healthrelated issues; or educational
information on specific medical
conditions (for example, flu shot
reminders), or referrals for Medicare
covered items and services.
Medicare fee-for-service beneficiary
means an individual who is—
(1) Enrolled in the original Medicare
fee-for-service program under parts A
and B; and
(2) Not enrolled in any of the
following:
(i) A MA plan under part C.
(ii) An eligible organization under
section 1876 of the Act.
(iii) A PACE program under section
1894 of the Act.
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Medicare Shared Savings Program
(Shared Savings Program) means the
program, established under section 1899
of the Act and implemented in this part.
One-sided model means a model
under which the ACO may share
savings with the Medicare program, if it
meets the requirements for doing so, but
is not liable for sharing any losses
incurred under the provisions of
§ 425.7(c).
Physician Quality Reporting System
means the system established under
section 1848(k) of the Act.
Primary care physician means a
physician (as defined at § 410.20(b)(1))
who has a primary specialty designation
of internal medicine, general practice,
family practice, or geriatric medicine.
Primary care services mean the set of
services identified by the following
HCPCS codes: 99201 through 99215,
99304 through 99340, and 99341
through 99350, G0402 (the code for the
Welcome to Medicare visit); and G0438
and G0439 (codes for the annual
wellness visits).
Reporting period means January 1
through December 31.
TIN means Federal taxpayer
identification number.
Two-sided model means a model
under which the ACO may share
savings with the Medicare program, if it
meets the requirements for doing so,
and is also liable for sharing any losses
incurred under the provisions of
§ 425.7(d).
Subpart B—Shared Savings Program
Requirements
§ 425.5 Eligibility and governance
requirements.
(a) General requirements. (1) Under
the Shared Savings Program, ACO
participants may work together to
manage and coordinate care for
Medicare fee-for-service beneficiaries
through an ACO that participates in the
Shared Savings Program and meets the
criteria specified in this part.
(2) ACOs that exceed a minimum
savings rate established under
§ 425.7(c)(2) and (d)(2), meet the
minimum quality performance
standards established under § 425.10,
and otherwise maintain their eligibility
to participate in the Shared Savings
Program under this section are eligible
to receive payments for shared savings
under § 425.7 of this subpart.
(3) ACOs that operate under the twosided model established in this section
must share losses with the Medicare
program under § 425.7 of this subpart.
(b) Eligible providers and suppliers.
The following ACO participants, which
must have established a mechanism for
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shared governance, are eligible,
separately or in combination, to form
ACOs that may participate in the Shared
Savings Program:
(1) ACO professionals in group
practice arrangements.
(2) Networks of individual practices
of ACO professionals.
(3) Partnerships or joint venture
arrangements between hospitals and
ACO professionals.
(4) Hospitals employing ACO
professionals.
(5) Providers or suppliers otherwise
recognized under the Act that are not
ACO professionals or hospitals, as
defined in § 425.4.
(6) CAHs that bill under Method II (as
described in § 413.70(b)(3))
(c) Reporting of TINs. (1) Each ACO
must report to CMS the TINs of the ACO
participants comprising the ACO along
with a list of associated National
Provider Identifiers (NPIs), at the
beginning of each performance year and
at other such times as specified by CMS.
(2) For purposes of the Shared
Savings Program, each ACO participant
TIN upon which beneficiary assignment
is dependent is required to commit to a
3-year agreement with CMS and will be
exclusive to one ACO.
(3) ACO participant TINs upon which
beneficiary assignment is not dependent
are required to commit to a 3-year
agreement to the ACO, and the ACO
participant must not be required to be
exclusive to a single ACO.
(d) Other requirements. (1)
Accountability for beneficiaries. As part
of its application and 3-year agreement,
the ACO must certify that the providers
and suppliers forming the ACO have
agreed to become accountable for and
report to CMS on the quality, cost, and
overall care of the Medicare fee-forservice beneficiaries assigned to the
ACO. Each ACO must make information
on its accountability for quality, cost,
and the overall care of its assigned
population available to the public in a
standardized format, as determined by
CMS.
(2) Coordination of Antitrust Agency
review. (i) Except for an ACO that
qualifies for the Rural Exception
articulated in the Antitrust Policy
Statement or other controlling guidance
from the antitrust agencies, an ACO
with a Primary Service Area (PSA)
share, as described in the Antitrust
Policy Statement, greater than 50
percent for any common service that
two or more ACO participants provide
to patients from the same PSA must do
both of the following:
(A) Request an expedited antitrust
review from the Antitrust Agencies.
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(B) Submit, as part of its application,
a letter from the reviewing Antitrust
Agency confirming that it has no
present intent to challenge or to
recommend challenging the proposed
ACO.
(ii) Except for an ACO that qualifies
for the Rural Exception articulated in
the Antitrust Policy Statement, or other
controlling guidance from the antitrust
agencies, an ACO with a PSA share, as
described in the Antitrust Policy
Statement, greater than 30 percent and
less than or equal to 50 percent may do
one of the following:
(A) Request an expedited antitrust
review from the Antitrust Agencies.
(B) Submit a letter from the reviewing
Antitrust Agency confirming that it has
no present intent to challenge or to
recommend challenging the proposed
ACO.
(C) Begin to operate and abide by a
list of conduct restrictions, reducing
significantly the likelihood of antitrust
concern.
(D) Begin to operate and remain
subject to antitrust investigation if it
presents competitive concerns.
(iii) An ACO must notify CMS at least
30 days before any material change
within the 3-year agreement period of
its ACO participants or ACO providers/
suppliers and must submit recalculated
PSA shares for common services that
two or more independent ACO
participants provide to patients from the
same PSA. If any revised PSA share is
calculated to be greater than 50 percent,
the ACO will be subject to review or rereview by an Antitrust Agency in order
to remain eligible to participate in the
Shared Savings Program.
(iv)(A) If an ACO receives a letter
from a reviewing Antitrust Agency
stating that the Antitrust Agency will
likely challenge or recommend
challenging the ACO, then the ACO will
be ineligible to participate in the Shared
Savings Program.
(B) The ACO must promptly inform
CMS if it receives such a letter at any
time from an Antitrust Agency.
(3) Agreement requirements. (i) Upon
being notified by CMS of its approval to
participate in the Shared Savings
Program, an executive of that ACO who
has the ability to legally bind the ACO
must sign and submit to CMS a 3-year
agreement.
(ii) The 3-year agreement must require
the ACO to comply with the provisions
in this part in order to participate in the
Shared Savings Program.
(iii) All contracts or arrangements
between or among the ACO, ACO
participants, ACO providers/suppliers,
and other entities furnishing services
related to ACO activities must require
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compliance with the requirements and
conditions of this part, including those
specified in the 3-year agreement. The
ACO must provide a copy of the 3-year
agreement to these individuals and
entities.
(iv)(A) The ACO must certify the
accuracy, completeness, and
truthfulness of its information contained
in the following:
(1) Shared Savings Program
application.
(2) 3-year agreement.
(3) Submissions of quality data and
other information.
(B) Certification must be made at the
time the ACO submits the following:
(1) Application to participate in the
Shared Savings Program.
(2) Executes the 3-year agreement.
(3) Submits any information,
including quality data, on which shared
savings payments or shared losses are
calculated.
(C) Certification must be signed by an
individual with the authority to legally
bind the ACO (for example the ACO’s
chief executive officer (CEO) or chief
financial officer (CFO)).
(v) The ACO must establish
partnerships with community
stakeholders in order to advance the
three-part aim of better care for
individuals, better health for
populations, and lower growth in
expenditures.
(vi) The ACO must agree, and must
require its ACO participants, ACO
providers/suppliers, and contracted
entities performing functions or services
on behalf of the ACO to agree, or to
comply with applicable provisions of
the following:
(A) Federal criminal law.
(B) The False Claims Act (31 U.S.C.
3729 et seq.).
(C) The anti-kickback statute (42
U.S.C. 1320a–7b(b)).
(D) The civil monetary penalties law
(42 U.S.C. 1320a–7a).
(E) The physician self-referral law (42
U.S.C. 1395nn).
(vii)(A) The ACO must agree, as a
condition of receiving any shared saving
payment and participating in the
program, that an individual with the
authority to legally bind the ACO must
certify that any data or information
requested by or submitted to CMS is
accurate, complete, and truthful.
(B) If data or information is generated
by an entity other than the ACO, such
entity must similarly certify the
accuracy, completeness, and
truthfulness of the information or data.
(4) Marketing materials. (i) Any ACO
marketing materials or activities, as
defined in § 425.4, must be approved by
CMS before use.
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(ii) Any changes to CMS-approved
marketing materials or activities must be
approved by CMS before use.
(5) Notice of ACO participation.
(i) ACO participants must notify
beneficiaries that their ACO providers/
suppliers are participating in an ACO.
(ii) Except as specified in paragraph
§ 412.1(a)(1) of this section, all
beneficiary communications any
materials or activities used by ACO
participants or ACO providers/suppliers
on behalf of the ACO to communicate
about the ACO in any manner to
Medicare beneficiaries, must be
approved by CMS before use.
(6) Tracks during agreement periods.
(i) For its initial agreement period, an
ACO may elect to operate under one of
the following tracks:
(A) Track 1. Under Track 1, the ACO
operates under the one-sided model (as
described under § 425.7(c) of this part)
for 2 years, and under the two-sided
model (as described under § 425.7(d) of
this part) for the third year. In the third
year of the ACO’s agreement under
Track 1, the methodology used to
reconcile ACOs under the first year of
the two-sided model would apply
except ACOs must meet the quality
performance standard that applies in the
third year.
(B) Track 2. Under Track 2, the ACO
operates under the two-sided model (as
described under § 425.7(d) of this part),
sharing both savings and losses with the
Medicare program for 3 years.
(ii) For subsequent agreement periods,
an ACO may operate only under the
two-sided model, sharing both savings
and losses with the Medicare program
(as described in § 425.7(d) of this part).
(iii) In both models an ACO’s share in
savings will be subject to 25 percent
withholding in order to help ensure
repayment of any losses to the Medicare
program. The withheld amount will be
applied towards repayment of an ACO’s
losses.
(iv) ACOs must obtain reinsurance,
place funds in escrow, obtain surety
bonds, establish a line of credit as
evidenced by a letter of credit that the
Medicare program can draw upon, or
establish another appropriate repayment
mechanism in order to ensure
repayment of any losses to the Medicare
program in advance of entering a period
of participation in the Shared Savings
Program under the two-sided model.
(v) An ACO that is applying for
participation in the Shared Savings
Program must, as part of its application,
submit documentation of such a
repayment mechanism for approval by
CMS. This documentation must include
details supporting the adequacy of the
mechanism for repaying losses equal to
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at least 1 percent of the ACO’s per
capita expenditures for its assigned
beneficiaries from the most recent year
available.
(iv) CMS will determine the adequacy
of an ACO’s repayment mechanism.
(v) An ACO must demonstrate the
adequacy of this repayment mechanism
annually, prior to the start of each
performance year in which it takes risk.
(vi) To the extent that such an ACO’s
repayment mechanism does not enable
CMS to fully recoup the losses for a
given performance year, any unpaid
losses will be carried forward into
subsequent performance years and
agreement periods (to be recouped
either against additional financial
reserves, or offset by shared savings
earned by the ACO).
(7) Legal structure. (i) An ACO must
be constituted as a legal entity for
purposes of all of the following:
(A) Receiving and distributing shared
savings.
(B) Repaying shared losses.
(C) Establishing, reporting, and
ensuring provider compliance with
health care quality criteria, including
quality performance standards.
(D) Other ACO functions identified in
this part.
(ii) An ACO must certify that it is
recognized as a legal entity in the State
in which it was established and that it
is authorized to conduct business in
each State in which it operates.
(8) Shared governance. (i) An ACO
must establish and maintain a governing
body with adequate authority to execute
the functions of an ACO as defined
under this part, including but not
limited to, the definition of processes to
promote evidence-based medicine and
patient engagement, report on quality
and cost measures, and coordinate care.
(ii) The governing body must be
comprised of the following:
(A) ACO participants or their
designated representatives.
(B) Medicare beneficiary
representative(s) served by the ACO
who do not have a conflict of interest
with the ACO, and who have no
immediate family member with conflict
of interest with the ACO.
(iii) The governing body must have
and possess broad responsibility for the
ACO’s administrative, fiduciary, and
clinical operations.
(iv) At least 75 percent control of the
ACO’s governing body must be held by
ACO participants. Each ACO participant
must choose an appropriate
representative from within its
organization to represent them on the
governing body and each ACO
participant must have appropriate
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proportionate control over governing
body decision making.
(v)(A) The members of the governing
body may serve in a similar or
complementary manner for an existing
participant in the ACO.
(B) The governing body of the ACO
must be separate and unique to the ACO
in cases where the ACO comprises
multiple, otherwise independent
entities (for example, several
independent physician group practices).
(C) The ACO must provide evidence
within its application that the governing
body is a separate legal entity.
(vi)(A) Except as specified in
paragraph (d)(8)(vi)(b) of this section, a
separate governing body must be
established.
(B) If the ACO is comprised of a single
entity that is financially and clinically
integrated, and if at least 75 percent
control of the entity’s governing body is
comprised of representatives of the
entity, the ACO governing body may be
the same as the governing body of that
entity, provided it satisfies the other
requirements of this section.
(9) Leadership and management
structure. (i) As part of its application
process, an ACO must submit
supporting materials to CMS that
demonstrate the ACO’s leadership and
management structure, including
clinical and administrative systems that
align with and support the goals of the
Shared Savings Program and the aims of
better care for individuals, better health
for populations, and lower growth in
expenditures.
(ii) The ACO’s operations must be
managed by an executive, officer,
manager, or general partner whose
appointment and removal are under the
control of the organization’s governing
body and whose leadership team has
demonstrated the ability to influence or
direct clinical practice to improve
efficiency processes and outcomes.
(iii) Clinical management and
oversight must be managed by a fulltime senior-level medical director who
is physically present on a regular basis
in an established ACO location, and
who is a board-certified physician and
licensed in the State in which the ACO
operates.
(iv) ACO participants and ACO
providers/suppliers must have a
meaningful commitment to the ACO’s
clinical integration program to ensure
its likely success. Meaningful
commitment may include, for example,
a meaningful financial investment in the
ACO or a meaningful human investment
(for example, time and effort) in the
ongoing operations of the ACO such that
the potential loss or recoupment of the
investment is likely to motivate the
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participant and provider/supplier to
make the clinical integration program
succeed.
(v) A physician-directed quality
assurance and process improvement
committee must oversee an ongoing
action-oriented quality assurance and
improvement program. The quality
assurance program must establish
internal performance standards for
quality of care and services, cost
effectiveness, and process and outcome
improvements, and hold ACO’s
providers/suppliers accountable for
meeting the performance standards. The
program must have processes and
procedures in place to identify and
correct poor compliance with such
standards and to promote continuous
quality improvements.
(vi) The ACO must implement
evidence-based medical practice or
clinical guidelines and processes for
delivering care consistent with the aims
of better care for individuals, better
health for populations, and lower
growth in health care expenditures. The
guidelines and care delivery processes
must cover diagnoses with significant
potential for the ACO to achieve quality
and cost improvements, taking into
account the circumstances of individual
beneficiaries.
(vii) ACO participants and providers/
suppliers must agree to comply with
these guidelines and processes and to be
subject to performance evaluations and
potential remedial actions, including
their expulsion from the ACO. The ACO
must have policies and procedures for
expulsion of ACO participants and ACO
provider/suppliers from the ACO.
(viii) The ACO must have an
infrastructure, such as information
technology (which may include EHR
technology certified to the standards
and implementation specifications
adopted by the Secretary for the
purposes of the meaningful use EHR
incentive programs), that enables the
ACO to collect and evaluate data and
provide feedback to ACO participants
and ACO providers/suppliers across the
entire ACO, including providing
information to influence care at the
point of care.
(ix) The supporting materials that are
submitted in the application must
include all of the following:
(A) ACO documents (for example,
participation agreements, employment
contracts, and operating policies) that
describe the ACO participants’ rights
and obligations in the ACO, including
distribution of shared savings to
encourage ACO participants and ACO
providers/suppliers to adhere to the
quality assurance and improvement
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program and the evidenced-based
clinical guidelines.
(B) Documents that describe the scope
and scale of the quality assurance and
clinical integration program, including
documents that describe all relevant
clinical integration program systems
and processes, such as the internal
performance standards and the
processes for monitoring and evaluating
performance.
(C) Supporting materials documenting
the ACO’s organization and
management structure, including an
organizational chart, a list of committees
(including names of committee
members) and their structures, and job
descriptions for senior administrative
and clinical leaders.
(D) Evidence that the ACO has a
board-certified physician as its medical
director who is licensed in the State in
which the ACO resides and that a
principal CMS liaison is identified in its
leadership structure.
(E) Evidence that the governing body
is comprised of representatives the ACO
participants who form the ACO, and
that these ACO participants comprise at
least 75 percent of the governing body.
(F) Upon request, the ACO must
provide copies of all documents
effectuating the ACO’s formation and
operation, including, without limitation
the following:
(1) Charters.
(2) By-laws.
(3) Articles of incorporation.
(4) Partnership agreement.
(5) Joint venture agreement.
(6) Management or asset purchase
agreements.
(7) Financial statements and records.
(8) Descriptions of the remedial
processes that will apply if an ACO
participant or an ACO provider/supplier
fails to comply with the ACO’s internal
procedures and performance standards,
including a CAP and the circumstances
under which expulsion from the ACO
could occur.
(G) A copy of the ACO’s compliance
plan or documentation describing the
plan that will be put in place at the time
the ACO’s agreement with CMS
becomes effective.
(H) A description of how the ACO
will partner with community
stakeholders.
(I) Written standards for beneficiary
access and communication. These
standards must include the ACO’s
process for beneficiaries to access their
medical record.
(x) CMS retains the right to give
consideration to an innovative ACO
with a management structure not
meeting these requirements.
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(10) Compliance plan. (i) The ACO
must have a compliance plan that
includes at least the following elements:
(A) A designated compliance official
or individual who is not legal counsel
and who has the ability to report
directly to the ACO’s governing body.
(B) Mechanisms for identifying and
addressing compliance problems related
to the ACO’s operations and
performance.
(C) A method for employees or
contractors of the ACO, ACO
participants, and ACO providers/
suppliers to report suspected problems
related to the ACO.
(D) Compliance training for the ACO,
the ACO participants, and the ACO
providers/suppliers.
(E) A requirement to report suspected
violations of law to an appropriate law
enforcement agency.
(ii) To achieve an effective
compliance program, an ACO may
consider coordinating its compliance
efforts with existing compliance efforts
of its ACO providers/suppliers.
(11) Distribution of savings. As part of
its application to participate in the
Shared Savings Program, an ACO must
describe how:
(i) It plans to use shared savings
payments, including the criteria it plans
to employ for distributing shared
savings among its participants.
(ii) The proposed plan will achieve
the specific goals of the Shared Savings
Program.
(iii) The proposed plan will achieve
the general aims of better care for
individuals, better health for
populations, and lower growth in
expenditures.
(12) Written request for shared
savings payment. (i) After receipt of
notification from CMS of the anticipated
shared savings payment or amount of
shared losses, an individual with the
authority to legally bind the ACO (such
as the ACO’s CEO or CFO), must make
a written request to CMS for payment of
the shared savings (or acknowledge the
amount of shared losses) in a document
that certifies the ACO’s compliance with
program requirements as well as the
accuracy, completeness, and
truthfulness of any information
submitted directly or indirectly by the
ACO, its ACO participants, the ACO
providers/suppliers, or any other entity
to CMS, including any quality data or
other information or data relied upon by
CMS in determining the ACO’s
eligibility for, and the amount of a
shared savings payment or the amount
owed by the ACO to CMS.
(ii) If such data are generated or
submitted by ACO participants, ACO
providers/suppliers, or another entity,
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such ACO participant, ACO provider/
supplier, must similarly certify the
accuracy, completeness, and
truthfulness of the data and provide the
government with access to such data for
audit, evaluation, investigation, and
inspection.
(13) Sufficient number of primary care
providers and beneficiaries. (i) CMS will
deem an ACO to have a sufficient
number of primary care physicians and
beneficiaries if the number of
beneficiaries historically assigned to the
ACO participants using the assignment
methodology in § 425.6 is 5,000 or more.
(ii) If at the end of a performance year,
an ACO’s assigned population falls
below 5,000, then that ACO will be
issued a warning and placed on a CAP.
(A) While under the CAP, an ACO
remains eligible for shared savings and
losses during that performance year.
(B) If the ACO’s assigned population
has not returned to at least 5,000 by the
end of the next performance year, then
that ACO’s agreement will be
terminated and the ACO will not be
eligible to share in savings for that year.
(14) Required reporting on
participating ACO professionals. A
participating ACO must maintain,
update, and annually report to CMS a
list of the following:
(i) Each ACO participant’s TIN.
(ii) Each ACO providers/supplier’s
NPI and/or TIN.
(15) Required processes and patientcenteredness criteria. (i) Required
processes. In its application to
participate in the Shared Savings
Program, an ACO must provide CMS
with documentation of its plans to do
all of the following:
(A) Promote evidence-based
medicine.
(B) Promote beneficiary engagement.
(C) Internally report quality and cost
metrics.
(D) Coordinate care.
(ii) Patient-centeredness criteria. (A)
An ACO should adopt a focus on
patient-centeredness that is promoted
by the governing body and integrated
into practice by leadership and
management working with the
organization’s health care teams.
(B) An ACO must demonstrate
patient-centeredness by addressing all
of the following areas:
(1) Have a beneficiary experience of
care survey in place (using the Clinician
and Group CAHPS survey, including an
appropriate functional status survey
module) and describe how the ACO will
use the results to improve care over
time.
(2) Patient involvement in ACO
governance.
(3) A process for evaluating the health
needs of the ACO’s assigned population,
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including consideration of diversity in
its patient populations, and a plan to
address the needs of its population.
(4) Systems in place to identify and
update high-risk individuals and
processes to develop individualized
care plans for targeted patient
populations including integration of
community resources to address
individual needs.
(i) Such plans must promote
improved outcomes for, at a minimum,
high-risk and multiple chronic
condition patients, and as appropriate,
other patients with chronic conditions.
(ii) The plan must be tailored to the
beneficiary’s health and psychosocial
needs, account for beneficiary
preferences and values, and identify
community and other resources to
support the beneficiary in following the
plan.
(5) A mechanism in place for the
coordination of care (for example, via
use of enabling technologies or care
coordinators).
(i) The ACO is required to describe its
mechanism for coordinating care for
Medicare beneficiaries.
(ii) The ACO should have a process in
place (or clear path to develop such a
process) to exchange summary of care
information when patients transition to
another provider or setting of care, both
within and outside the ACO.
(iii) For providers enrolled in the
electronic exchange of information, this
process must be consistent with
meaningful use requirements under the
Medicare EHR Incentive Program (as
described in part 495 of this chapter).
(6) A process in place for
communicating clinical knowledge/
evidence-based medicine to
beneficiaries in a way that is
understandable to them.
(7) A process in place for beneficiary
engagement and shared decision-making
that takes into account the beneficiaries’
unique needs, preferences, values, and
priorities.
(8) Written standards in place for
beneficiary access and communication,
and a process in place for beneficiaries
to access their medical record.
(9) Internal processes in place for
measuring clinical or service
performance by physicians across the
practices, and using these results to
improve care and service over time.
§ 425.6 Assignment of Medicare fee-forservice beneficiaries to ACOs.
(a) General rule. (1) Medicare fee-forservice beneficiaries are assigned to an
ACO based on their utilization of
primary care services provided under
this title by a primary care physician
who is an ACO provider/supplier
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during the performance year for which
shared savings are to be determined.
(2) Beneficiary assignment to an ACO
is for purposes of determining the
population of Medicare fee-for-service
beneficiaries for whose care the ACO is
accountable, and for determining
whether an ACO has achieved savings
under § 425.7 of this part, and in no way
diminishes or restricts the rights of
beneficiaries assigned to an ACO to
exercise free choice in determining
where to receive health care services.
(b) Assignment methodology. CMS
employs the following methodology to
assign Medicare beneficiaries to an
ACO:
(1) For each ACO, identify all primary
care physicians as defined in § 425.4 of
this part who were an ACO participant
during the performance year.
(2) At the end of each performance
year, determine all beneficiaries who
received services from primary care
physicians in the ACO, as determined
under paragraph (b)(1) of this section.
(3) Determine the total allowed
charges for the primary care services (as
identified by HCPCS code in the
definition of primary care services
under § 425.4 of this section) that each
of the beneficiaries identified in
paragraph (b)(2) received from any
provider or supplier during the
performance year.
(4) For each beneficiary, add together
the allowed charges for the primary care
services provided by the primary care
physicians (identified in paragraph
(b)(1) of this section) in each ACO
(identified in paragraph (b)(1) of this
section).
(5) Assign a beneficiary to an ACO if
the beneficiary has received a plurality
of his or her primary care services, as
determined by the sum of allowed
charges for those services under
paragraph (b)(4) of this section, from
primary care physicians identified
under paragraph (b)(1) of this section,
who are an ACO participant.
(c) Beneficiary information and
notification. ACO participants will post
signs in each of their facilities and
provide written notification for
beneficiaries about their participation in
the Shared Savings Program.
§ 425.7
Payment and treatment of savings.
(a) Establishing a benchmark. (1)
Using a 6-months claims run-out, CMS
will retrospectively estimate and update
an ACO’s benchmark for an agreement
period starting with ACO participants
identified at the start of the agreement
period.
(2) Using the claim records of ACO
participants and applying the
methodology for assigning beneficiaries
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in § 425.6 of this part, CMS will
compute per capita expenditures for
beneficiaries who would have been
assigned to the ACO in any of the prior
three most recent available years.
(b) Computing per capita Medicare
Part A and Part B expenditures and
updating the benchmark. In computing
these per capita expenditures, CMS uses
the per capita Parts A and B fee-forservice expenditures for beneficiaries
that would have been assigned to the
ACO in each of these 3 prior years, we
will estimate a fixed benchmark that is
adjusted for overall growth and
beneficiary characteristics, including
health status using prospective HCC
adjustments. This benchmark will then
be updated annually during the
agreement period, according to statute,
based on the absolute amount of growth
in national per capita expenditures for
Parts A and B services under the
original Medicare fee-for-service
program. CMS will do all of the
following:
(1) Calculate annual Parts A and B
fee-for-service per capita expenditures
for the beneficiaries who would have
been assigned for each of the benchmark
years. To minimize variation from
catastrophically large claims, CMS
truncates an assigned beneficiary’s
total—
(i) Parts A and B fee-for-service per
capita expenditures at the 99th
percentile as determined for each
benchmark year.
(2) Using CMS Office of the Actuary
national Medicare expenditure data for
each of the years making up the
benchmark, CMS determines national
growth trend indices and trend them to
the third benchmark year (BY3) dollars.
(3) Using health status measures for
the beneficiary population in each of the
years making up the benchmark, CMS
establishes health status indices for each
year and adjust these indices so they are
restated in BY3 risk.
(4) CMS computes a 3-year risk-and
growth-trend adjusted per capita
expenditure amount for the patient
populations in each of the 3 benchmark
years by combining the initial per capita
expenditures for each year with the
respective growth and health status
indices. The result is risk adjusted per
capita expenditures for beneficiaries
historically assigned to the ACO in each
of the 3 years used to establish the
benchmark stated in BY3 risk and
expenditure amounts, and assigned
patient populations.
(5) CMS weights the most recent year
of the benchmark, BY3 at 60 percent,
BY2 at 30 percent and BY1 at 10 percent
to ensure that the benchmark reflects
more accurately the latest expenditure
and health status of the ACO’s assigned
beneficiary population.
(6) CMS updates this fixed benchmark
by the projected absolute amount of
growth in national per capita
expenditures for Parts A and B services
under the original Medicare fee-forservice program using data from CMS’s
Office of the Actuary.
(7) In performing these steps, CMS
does not take into consideration
expenditure increases or decreases
under Section 1848 related to valuebased purchasing programs or the
HITECH Act; specifically, any of the
following:
(i) Physician Quality Reporting
Initiative as provided in § 414.90.
(ii) Electronic prescribing program as
provided in § 414.92.
(iii) HITECH Act incentives for
eligible professionals as provided in
§ 495.102.
(c) Determination of savings and
shared savings rate for ACOs under the
one-sided model. (1) Savings
determination. For each performance
year, CMS determines whether the
estimated average per capita Medicare
expenditures under the ACO for
Medicare fee-for-service beneficiaries
for Parts A and B services, adjusted for
beneficiary characteristics, is below the
applicable benchmark determined
under paragraph (b) of this section. To
minimize variation from
catastrophically large claims, CMS
truncates that assigned beneficiary’s
total annual Parts A and B fee-forservice per capita expenditures at the
99th percentile as determined for each
performance year. In order to qualify for
a shared savings payment, the ACO’s
average per capita Medicare
expenditures for the performance year
must be below the applicable
benchmark by more than a minimum
savings rate established for the ACO
under paragraph (c)(2) of this section.
(2) Minimum savings rate (MSR). CMS
computes a minimum savings rate for
each ACO based on the number of
beneficiaries assigned to the ACO under
§ 425.6 of this part. The minimum
savings rates for ACOs based on the
numbers of assigned beneficiaries will
be as follows:
MSR (low end of
assigned
beneficiaries)
%
Number beneficiaries
5,000–5,999 .................................................................................................................................................
6,000–6,999 .................................................................................................................................................
7,000–7,999 .................................................................................................................................................
8,000–8,999 .................................................................................................................................................
9,000–9,999 .................................................................................................................................................
10,000–14,999 .............................................................................................................................................
15,000–19,999 .............................................................................................................................................
20,000–49,999 .............................................................................................................................................
50,000–59,999 .............................................................................................................................................
3.9
3.6
3.4
3.2
3.1
3.0
2.7
2.5
2.2
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60,000 + .......................................................................................................................................................
(3) Qualification for shared savings
payment. In order to qualify for shared
savings, an ACO must exceed its
minimum savings rate determined
under paragraph (c)(2) of this section,
meet the minimum quality performance
standards established under § 425.10 of
this part, and otherwise maintain its
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eligibility to participate in the Shared
Savings Program under this part.
(4) Net savings threshold. An ACO
under the one-sided model that exceeds
its minimum savings rate is eligible to
share savings net 2 percent of its
benchmark as determined under
§ 425.7(b). An ACO with fewer than
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MSR (high end of
assigned
beneficiaries)
%
3.6
3.4
3.2
3.1
3.0
2.7
2.5
2.2
2.0
2.0
10,000 assigned beneficiaries in the
most recent year for which CMS has
complete claims data, and that meets
any one of the following criteria, is
exempt from the 2 percent net savings
threshold adjustment under the onesided model:
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(d) Determination of savings or losses,
and shared savings or loss rates for
ACOs under the two-sided model. (1)
For each performance year, CMS
determines whether the estimated
average per capita Medicare
expenditures under the ACO for
Medicare fee-for-service beneficiaries
for parts A and B services, adjusted for
beneficiary characteristics, is above or
below the benchmark determined under
paragraph (b) of this section. In order to
qualify for a shared savings payment
under the two-sided model, or to be
responsible for sharing losses with CMS,
an ACO’s average per capita Medicare
expenditures for the performance year
must be below or above the benchmark,
respectively, by more than the
minimum savings or loss rate under
paragraph (d)(2) of this section.
(2) Minimum savings or loss rate. (i)
To qualify for shared savings under the
two-sided model, an ACO’s average per
capita Medicare expenditures for the
performance year must be below its
benchmark costs for the year by at least
2 percent.
(ii) To be responsible for sharing
losses with the Medicare program, an
ACO’s average per capita Medicare
expenditures for the performance year
must be at least 2 percent above its
benchmark costs for the year.
(3) Qualification for shared savings
payment. To qualify for shared savings,
an ACO must meet the minimum
savings rate requirement established
under paragraph (d)(2) of this section,
meet the minimum quality performance
standards established under § 425.10 of
this part, and otherwise maintain its
eligibility to participate in the Shared
Savings Program under this part.
(4) Final sharing rate. The final
sharing rate for an ACO in the two-sided
model will be calculated by adding the
ACO’s earned quality performance
sharing rate under paragraph (d)(5) and
any additional increase described in
§ 425.7(c)(6)) up to the performance
payment limit described in
§ 425.7(d)(7).
Percentage of ACO
(5) Quality performance sharing rate.
assigned benePercentage point inficiaries with 1 or
crease in shared sav- An ACO that meets all the requirements
more visits to an
ings rate (one-sided
for receiving shared savings payments
FQHC/RHC during
model)
under the two-sided model will receive
the performance year
a payment of up to 60 percent of all the
1–10
0.5 savings under the benchmark as
determined on the basis of its quality
11–20
1
21–30
1.5 performance under § 425.10 of this part.
(6) Additional increase to the shared
31–40
2
41–50
2.5 savings rate. Under the two-sided
model, an ACO’s shared savings rate
(8) Performance payment limit. The
may be increased by the following up to
amount of shared savings an eligible
5.0 percentage points if the ACO
ACO receives under the one-sided
includes a RHC or FQHC (as these terms
model may not exceed 7.5 percent of its are defined under § 405.2401(b) of these
benchmark.
regulations) within its structure,
srobinson on DSKHWCL6B1PROD with PROPOSALS2
(i) All ACO participants are
physicians or physician groups.
(ii) 75 percent or more of the ACO’s
assigned beneficiaries reside in counties
outside an MSA in the most recent year
for which CMS has complete claims
data.
(iii) 50 percent or more of an ACO’s
assigned beneficiaries in the most recent
year for which CMS has complete
claims data were assigned on the basis
of services received from Method II
CAHs.
(iv) At least 50 percent of the assigned
beneficiaries had at least one encounter
with a participating FQHC or RHC in
the most recent year for which CMS has
complete claims data such that the ACO
has achieved maximum sharing for this
activity.
(5) Final sharing rate. The final
sharing rate for an ACO in the one-sided
model will be calculated by adding the
ACO’s earned quality performance
sharing rate and any additional increase
described in § 425.7(c)(6)) (up to the
performance payment limit described in
§ 425.7(c)(7)).
(6) Quality performance sharing rate.
An ACO that meets all the requirements
for shared savings payments under the
one-sided model will receive a shared
savings payment based on quality
performance of up to 50 percent, as
determined on the basis of its quality
performance under § 425.10 of this part.
(7) Additional increase to the shared
savings rate. Under the one-sided
model, an ACO’s shared savings rate
may be increased by up to 2.5
percentage points if the ACO includes a
rural health clinic (RHC) or Federally
qualified health center (FQHC) (as
defined under § 405.2401(b) of this
chapter) within its structure,
determined on a sliding scale based on
the number of assigned Medicare
beneficiaries with one or more visit to
an RHC or FQHC during the
performance year. The sliding scale will
operate according to the following table:
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19647
determined on a sliding scale based on
the number of assigned Medicare
beneficiaries with one or more visit to
an RHC or FQHC during the
performance year. The sliding scale will
operate according to the following table:
Percentage of ACO
assigned beneficiaries
with 1 or more visits
to an FQHC/RHC during the performance
year
Percentage point increase in shared savings rate (one-sided
model)
1–10
11–20
21–30
31–40
41–50
1.0
2.0
3.0
4.0
5.0
(7) Performance payment limit. The
amount of shared savings an eligible
ACO receives under the two-sided
model may not exceed 10 percent of its
benchmark.
(8) Shared loss rate. The shared loss
rate for an ACO that is required to share
losses with the Medicare program for
expenditures over the benchmark with
the Medicare program is determined
based on the inverse of its final sharing
rate described in paragraphs (d)(2)
through (6) of this section (that is, 1
minus the shared savings rate
determined under paragraphs (d)(2)
through (6) of this section).
(9) Loss recoupment limit. The
amount of shared losses for which an
eligible ACO is liable may not exceed
the following percentages of its
benchmark as determined under
paragraphs (a) and (b) of this section: 5
percent in the first year of participation
in a two-sided model under the Shared
Savings Program, 7.5 percent in the
second year, and 10 percent in the third
year. An ACO in Track 1 who has
entered the third year of its agreement
period would be liable for an amount
not to exceed the percentage of the first
year of the two-sided model, that is, it
would not exceed 5 percent.
(e) Notification of savings and losses.
CMS notifies an ACO in writing
regarding whether the ACO qualifies for
a shared savings payment, and if so, the
amount of the payment due. Similarly,
CMS will provide written notification to
an ACO of the amount of shared losses,
if any, that it must pay to the program.
If an ACO has shared losses, the ACO
must make payment in full to CMS
within 30 days of receipt of notification.
§ 425.8 ACO quality and continuous
improvement goals.
(a) CMS defines quality and
continuous improvement goals for
ACOs.
(b) An ACO must meet the quality and
continuous improvement goals defined
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by CMS under paragraph (a) of this
section in order to qualify for shared
savings.
§ 425.9 Measures to assess the quality of
care furnished by an ACO.
(a) Selecting measures. CMS selects
the measures designated to determine
an ACO’s success in promoting the aims
of better care for individuals, better
health for populations, and lower
growth in expenditures.
(b) Quality measures for quality
performance standards. (1) CMS
designates the measures for use in the
calculation of the quality performance
standard.
(2) ACOs must submit data on the
measures determined under this
paragraph (b) according to the method
of submission established by CMS.
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§ 425.10 Calculating the ACO quality
performance score and determining shared
savings eligibility.
(a) Measure domains. CMS groups
individual quality performance standard
measures into five domains:
(1) Patient/care giver experience.
(2) Care coordination.
(3) Patient safety.
(4) Preventative health.
(5) At-risk population/frail elderly
health.
(b) Methodology for calculating a
performance score for each measure. (1)
CMS designates quality performance
standards for each measure, including a
performance benchmark and minimum
attainment level and establishes a point
scale for certain measures. Contingent
upon data availability, quality measure
performance benchmarks are defined by
CMS based on Medicare fee-for-service,
MA, or ACO performance data.
(i) For the first performance period
under the Shared Savings Program, CMS
defines the quality performance
standard at the level of complete and
accurate reporting.
(ii) For all subsequent years, CMS
defines the quality performance based
on measure scores.
(2) Performance below the minimum
attainment level will receive zero points
for that measure, for those measures in
which the points scale applies.
(3) Performance equal to or greater
than the minimum attainment level but
less than the performance benchmark
must receive points on a sliding scale
based on the level of performance, for
those measures in which the points
scale applies.
(4) Those measures designated as all
or nothing measures receive the
maximum available points if all criteria
are met and zero points if at least one
of the criteria are not met.
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(c) Methodology for calculating a
performance score for each domain.
CMS designates quality performance
standards for each domain’s
contribution to an overall ACO
performance score.
(d) Shared savings eligibility. If the
ACO demonstrates to CMS that it has
satisfied the quality performance
requirements for each domain, the
requirements of § 425.7 are satisfied,
and the ACO meets all other applicable
requirements, the ACO is eligible for
shared savings. To satisfy the quality
performance requirements for a domain:
(1) The ACO must report all measures
within a domain, via the mechanisms
determined by CMS, in order to be
considered for shared savings for that
domain.
(2) CMS scores individual measures
based on data received.
(3) CMS adds the individual scores for
each of the measures within the domain
to determine the domain scores.
(i) Each of the 5 domains is equally
weighted in determining an ACO’s
overall quality performance score,
regardless of whether the ACO is in
Track 1 or Track 2. All measures within
a domain must have a score above the
minimum attainment level determined
by CMS in order for the domain to be
eligible for shared savings.
(ii) If the ACO satisfies the quality
performance standards for one or more
domains, and also satisfies the
requirements for realizing shared
savings under § 425.7, the ACO may
receive the proportion of those shared
savings for which it qualifies.
(iii) CMS retains the right to audit and
validate quality data reported by an
ACO. In an audit, the ACO would be
required to provide beneficiary medical
record data as requested by CMS. The
audit would consist of three phases of
medical record review. If, at the
conclusion of the third audit process
there is a discrepancy greater than 10
percent between the quality data
reported and the medical records
provided, the ACO will not be given
credit for meeting the quality target for
any measures for which this mismatch
rate exists.
(iv) Failure to report quality measure
data accurately, completely, and timely
(or to timely correct such data) may
subject the ACO to termination or other
sanctions, as described in § 425.12.
(4) In the third year of the ACO’s
agreement under Track 1, the
methodology used to reconcile ACOs
under the first year of the two-sided
model would apply except that ACOs
must meet the quality performance
standard that applies in the third year,
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as opposed to the first year standard of
full and accurate reporting.
§ 425.11 Incorporating other reporting
requirements related to the Physician
Quality Reporting System and electronic
health records technology.
(a) Physician quality reporting system.
(1) ACOs, on behalf of their eligible
professionals, must submit the measures
determined under § 425.10(b) according
to the method of submission established
by CMS, to qualify for a Physician
Quality Reporting System incentive
under the Shared Savings Program.
(2) To qualify as a group practice for
a Physician Quality Reporting System
incentive under the Shared Savings
Program, eligible professionals within
an ACO must report the measures
determined under § 425.10(b) during the
reporting period according to the
method of submission established by
CMS under the Shared Savings Program.
(3) The Physician Quality Reporting
System incentive under the Medicare
Shared Savings Program is equal to 0.5
percent of the ACO’s eligible
professional’s total estimated Medicare
Part B Physician Fee Schedule allowed
charges for covered professional
services furnished during the calendar
year reporting period from January 1
through December 31.
(b) Electronic health records
technology. (1) At least 50 percent of an
ACO’s primary care physicians must be
meaningful EHR users, using certified
EHR technology as defined in § 495.4, in
the HITECH Act and subsequent
Medicare regulations by the start of the
second performance year in order to
continue participating in the Shared
Savings Program.
(2) CMS may terminate an ACO
agreement under § 425.14 of this part if
fewer than 50 percent of an ACO’s
primary care physicians are not
meaningfully EHR users, using certified
EHR technology as defined in § 495.4,
the HITECH Act and subsequent
Medicare regulations by the start of the
ACO’s second performance year.
§ 425.12
Monitoring.
(a) Monitoring of ACOs: General rule.
(1) CMS monitors and assesses the
performance of ACOs and their
participating providers/suppliers.
(2) CMS employs a range of methods
to monitor and assess the performance
of ACOs, including but not limited to
any of the following, as appropriate:
(i) Analysis of specific financial and
quality measurement data reported by
the ACO as well as aggregated annual
and quarterly reports.
(ii) Site visits.
(iii) Analysis of beneficiary and
provider complaints.
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(iv) Audits (including, for example,
analysis of claims, chart review
(medical record), beneficiary survey
reviews, coding audits).
(b) Monitoring ACO avoidance of atrisk beneficiaries. To identify ACOs that
could be avoiding at-risk beneficiaries,
CMS uses a combination of the methods
described in paragraph (a)(2) of this
section (as appropriate) to identify
trends and patterns suggestive of
avoidance of at-risk beneficiaries. The
results of these analyses may
subsequently require further
investigation and follow-up with the
beneficiary or the ACO and its ACO
providers/suppliers in order to
substantiate cases of beneficiary
avoidance. CMS may take the following
actions as set forth in § 425.13(a)(4) of
this part, if it determines that an ACO,
its ACO participants, any ACO
providers/suppliers, or contracted
entities performing functions or services
on behalf of the ACO avoids at-risk
beneficiaries.
(1) The ACO is required to submit a
CAP and implement the plan as
approved by CMS as set forth in
§ 425.13(a)(2) of this part.
(i) The ACO will not receive any
shared savings payments during the
probation period, regardless of the
period of performance for which savings
were attributable to while under the
CAP.
(ii) The ACO will not be eligible to
receive shared savings for the
performance period attributable to the
time the ACO was under the CAP.
(iii) The ACO will not be eligible to
earn shared savings attributable to the
time the ACO is under the CAP.
(iv) The ACO will be re-evaluated
during and after the CAP
implementation period to determine if
the ACO has continued to avoid at-risk
beneficiaries.
(2) ACO may be terminated if CMS
determines that the ACO has continued
to avoid at-risk beneficiaries during or
after the CAP as set forth in § 425.14 of
this part.
(c) Monitoring ACO compliance with
quality performance standards. To
identify ACOs that are not meeting the
quality performance standards, CMS
will review the ACO’s submission of
quality measurement data under
§ 425.9(b)(2). CMS may request
additional documentation from an ACO,
ACO participants, or ACO providers/
suppliers, as appropriate. CMS may take
the following actions, in addition to
actions set forth at § 425.13, if an ACO
does not meet quality performance
standards or fails to report on one or
more quality measures.
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(1) The ACO will be given a warning
for the first time it fails to meet the
minimum attainment level for one or
more domain.
(2) The ACO’s compliance with the
quality performance standards will be
re-evaluated the following year. If the
ACO continues to fail to meet quality
performance standards in the following
year, the agreement may be terminated
immediately or CMS may take an
alternative action as set forth in § 425.13
of this part.
(3) If an ACO fails to report one or
more quality measures or fails to report
completely and accurately on all
measures in a domain, CMS will request
the ACO either to submit the required
measure data, correct the data, and/or
provide a written explanation as to why
it did not report completely and
accurately. If ACO still fails to report,
fails to report by the requested deadline
and/or does not provide reasonable
explanation for not reporting, the ACO
will be terminated immediately as set
forth in § 425.14 of this part.
(4) An ACO that exhibits a pattern of
inaccurate or incomplete reporting, or
fails to make timely corrections
following notice to resubmit, may be
terminated from the program.
(d) Monitoring changes to ACO
eligibility requirements. In order to
ensure that the ACO continues to meet
the eligibility requirements under
§ 425.5 of this part, CMS uses a
combination of the methods described
in paragraph (a) of this section (as
appropriate).
(e) Monitoring beneficiary notification
of the provider and supplier’s role in the
ACO and the ability for the beneficiary
to op-out of sharing claims data. In
order to ensure that the ACO is
notifying beneficiaries concerning
sharing of claims data as provided
under § 425.15 of these regulations, and
providing the opportunity for a
beneficiary to opt-out of those data
sharing arrangements, as required by
that section, CMS uses a combination of
the methods described in paragraph (a)
of this section (as appropriate).
(f) Monitoring ACO marketing
materials and activities. (1) CMS may
monitor compliance with the
requirement for approval of ACO
marketing materials and activities set
forth in § 425(d)(4).
(2) An ACO that fails to adhere to this
requirement may be placed under a CAP
or terminated as set forth in § 425.14 of
this part, at the discretion of CMS.
§ 425.13
Actions prior to termination.
(a) If based upon the monitoring
activities described in § 425.12, CMS
concludes that an ACO’s performance
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may subject the ACO to termination
from the Shared Savings Program, CMS,
in its sole discretion, may take one or
more or all of the following actions prior
to termination of the ACO from the
Shared Savings Program.
(1) Provide a warning notice to the
ACO of the specific performance at
issue.
(2) Request a CAP from the ACO.
(i) The ACO must submit a CAP for
CMS approval by CMS deadline
indicated on the notice of violation.
(ii) The CAP must address what
actions the ACO will take to ensure that
the ACO, ACO participants, and ACO
providers/suppliers and/or contracted
entities performing services or functions
on behalf of the ACO will correct any
deficiencies and remain in compliance
with Shared Savings Program
requirements.
(iii) The ACO’s performance will be
monitored during the CAP process.
(iv) Failure to submit, obtain approval
for, or implement a CAP may result in
termination of the agreement.
(v) ACO failure to demonstrate
improved performance upon completion
of the CAP may result in termination.
(vi) This CAP process does not apply
to determinations made by the Antitrust
Agencies and must not be construed to
negate, diminish, or otherwise alter the
applicability of existing laws, rules, and
regulations, or determinations made by
other government agencies.
(3) Place the ACO on a special
monitoring plan.
(4) These procedures do not apply to
either of the following:
(i) Determinations that an ACO has
violated the Sherman antitrust act (15
U.S.C. 1), Clayton Act (15 U.S.C. 12), or
the Federal Trade Commission Act (15
U.S.C. 45).
(ii) Determinations made by other
government agencies.
(5) The procedures established under
this section do not negate, diminish, or
otherwise alter the applicability of
existing laws, rules, and regulations.
§ 425.14 Termination, suspension, and
repayment of Shared Savings.
(a) Grounds for terminating an ACO
agreement. CMS may terminate an
agreement with an ACO if the ACO, the
ACO participants, the ACO providers/
suppliers or contracted entities
performing services or functions on
behalf of the ACO:
(1) Avoid at-risk beneficiaries.
(2) Fail to meet quality performance
standards.
(3) Fail to completely and accurately
report information or fail to make timely
corrections to reported information.
(4) Are not in compliance with
eligibility requirements or have fallen
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out of compliance with the
requirements of the part because the
ACO has undergone material changes
that affect the ACO’s eligibility to
participate in the Shared Savings
Program, including, but not limited to
changes in governing body composition,
a significant change (as defined in
§ 425.21(b)), and the imposition of
sanctions or other actions taken against
the ACO by an accrediting organization,
State, Federal or local government
agencies.
(5) Are unable to effectuate any
required regulatory changes during the
agreement period after given the
opportunity for a CAP as set forth in
§ 425.20.
(6) Are not in compliance with
requirements to notify beneficiaries of
ACO provider/supplier participation in
an ACO.
(7) Engage in material noncompliance,
or demonstrates a pattern of
noncompliance, with public reporting
and other CMS reporting requirements.
(8) Fail to submit an approvable CAP,
fail to implement an approved CAP, or
fail to demonstrate improved
performance after the implementation of
a CAP.
(9) Violate the physician self-referral
prohibition, civil monetary penalties
(CMP) law, Anti-kickback statute, other
antifraud and antitrust laws (or enter
into a final judgement or other final
resolution of antitrust charges by an
Antitrust Agency), or any other
applicable Medicare laws, rules, or
regulations that are relevant to ACO
operations.
(10) Submit to CMS false, inaccurate,
or incomplete data and or information,
including but not limited to,
information provided in the Shared
Savings Program application, quality
data, financial data, and information
regarding the distribution of shared
savings.
(11) Use marketing materials or
participate in activities or other
beneficiary communications, that are
subject to review and approval, that
have not been approved by CMS.
(12) Fail to maintain an assigned
beneficiary population of at least 5,000
beneficiaries.
(13) Fail to offer beneficiaries the
option to opt-out of sharing claims
information.
(14) Limit or restrict internally
compiled beneficiary summary of care
or medical records from other
providers/suppliers both within and
outside of the Shared Savings Program
to the extent permitted by law.
(15) Improperly use or disclose claims
information received from CMS in
violation of the HIPAA Privacy Rule,
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Medicare Part D Data Rule, Privacy Act,
or the data use agreement.
(16) Fail to demonstrate that the ACO
has adequate resources in place to repay
losses and to maintain those resources
for the agreement period.
(b) Reapplication after termination.
An ACO that has been terminated from
the Shared Savings Program may apply
to participate in the Shared Savings
Program again only after the end of the
original 3-year agreement period.
(i) To be eligible to participate in the
Shared Savings Program, the ACO must
demonstrate in its application that it has
corrected the deficiencies that caused it
to be terminated from the Shared
Savings Program and has processes in
place to ensure that it will remain in
compliance with the terms of the new
participation agreement.
(ii) ACOs with corrected deficiencies
that wish to reenter the program have
the option to do so only under the twosided model.
(c) Forfeiture of mandatory
withholding after termination. If an
agreement is terminated for any reason
before the 3-year agreement period is
completed, the ACO the ACO would
forfeit its mandatory 25 percent
withhold of shared savings.
(d) Termination of an agreement by
an ACO. (1) ACO must notify CMS, its
ACO participants, and other
organizations of its decision to
terminate 60 days before the date of
termination.
(2) The ACO participants must notify
beneficiaries of the ACO’s decision to
terminate in a timely manner.
(3) All termination notification
materials must meet marketing
guidelines as set forth at § 425.12(f).
(e) Grounds for shared saving
payment suspension. If an ACO has
been placed under a CAP because the
ACO, ACO participants, ACO providers/
suppliers, or contracted entities
performing services or functions on
behalf of the ACO were found to have
avoided at-risk beneficiaries—
(1) The ACO must not receive shared
savings payments while it is under the
CAP, regardless of the period of
performance it is attributable to; and
(2) The ACO is not eligible to earn any
shared savings for the performance
period attributable for the time the ACO
was under the CAP.
§ 425.15
Reconsideration review process.
(a) There is no reconsideration,
appeals, or other administrative or
judicial review of the following
determinations under this section:
(1) The specification of quality and
performance standards under § 425.9 of
this part.
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(2) The assessment of the quality of
care furnished by an ACO under the
performance standards established in
§ 425.10.
(3) The assignment of Medicare feefor-service beneficiaries under § 425.6 of
this part.
(4) The determination of whether an
ACO is eligible for shared savings under
§ 425.7(c) of this part, and the amount
of such shared savings, including the
determination of the estimated average
per capita Medicare expenditures under
the ACO for Medicare fee-for-service
beneficiaries assigned to the ACO and
the average benchmark for the ACO
under § 425.7(a) and (b) of this part.
(5) The percent of shared savings
specified by the Secretary and the limit
on the total amount of shared savings
established under § 425.7(c) of this part.
(6) The termination of an ACO for
failure to meet the quality performance
standards established under § 425.14 of
this part.
(7) A determination made by the
reviewing antitrust agency that it is
likely to challenge or recommend
challenging the ACO.
(b) An ACO may appeal an initial
determination that is not prohibited
from administrative or judicial review
under paragraph (a) of this section by
requesting a reconsideration review by a
CMS reconsideration official.
(1) An ACO that wants to request
reconsideration review by a CMS
reconsideration official must submit a
written request by an authorized official
for receipt by CMS within 15 days of the
notice of the initial determination.
(i) If the 15th day is a weekend or a
Federal holiday, then the timeframe is
extended until the end of the next
business day.
(ii) Failure to submit a request for
reconsideration within 15 days will
result in denial of the request for
reconsideration.
(2) The reconsideration review may be
held orally (that is, in person, by
telephone or other electronic means) or
on the record (review submitted
documentation) at the discretion of the
reconsideration official.
(3) The reconsideration official will
send an acknowledgement of the
reconsideration review request to the
ACO and CMS that includes the
following:
(A) Review procedures.
(B) Procedures for submission of
evidence including format and
timelines.
(C) Date, time and location of the
review. The reconsideration official
may, on his or her own motion, or at the
request of CMS or the ACO, change the
time and place for the reconsideration
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review, but must give the parties to the
reconsideration review notice of the
change.
(4) The burden of proof is on the ACO
to demonstrate to the reconsideration
official with convincing evidence that
the initial determination is not
consistent with CMS’ regulations or
statutory authority.
(i) The reconsideration official’s
review will be based only on evidence
submitted by the reconsideration
official’s requested deadline, unless
requested by the reconsideration
official.
(ii) Documentation submitted for the
record as evidence cannot be
documentation that was not previously
submitted to CMS by its required
applicable timelines and in the
requested format.
(iii) All evidence submitted both from
the applicant and CMS, in preparation
for the reconsideration review will be
shared with participating parties prior
to the scheduled date of the hearing, as
indicated in the acknowledgement
notice.
(iv) All parties will be notified of the
reconsideration official’s
recommendation.
(c) If any of the parties disagree with
the recommendation of the
reconsideration official, they may
request an on the record review of the
initial determination and
recommendation by an independent
CMS official who was not involved in
the initial determination or the
reconsideration review process.
(1) Any party that wishes to request
an on the record review of the
reconsideration official’s
recommendation must submit an
explanation of why they disagree with
the recommendation by the timeframe
and in the format indicated on the
recommendation letter.
(2) The on the record review process
will be based only on evidence
presented for the reconsideration
review.
(3) The CMS official will consider the
recommendation of the reconsideration
official and make a final agency
determination.
(d) CMS’s decision after review of the
reconsideration official’s
recommendation is final and binding.
(e) The review process under this
section shall not be construed to negate,
diminish, or otherwise alter the
applicability of existing laws, rules, and
regulations or determinations made by
other government agencies.
(f) If CMS’ initial decision to deny an
ACO’s application to participate in the
Shared Savings Program is upheld, the
application will remain denied based on
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the effective date of the original notice
of denial.
(g) An ACO that requests a
reconsideration review for termination
will remain operational throughout the
review process. If CMS initial
determination to terminate the
agreement with the ACO is upheld,
termination of the agreement is effective
as indicated in the initial notice of
termination.
(1) If CMS’ initial determination to
terminate an agreement with an ACO is
upheld, the decision to terminate the
agreement is effective as of the date
indicated in the initial notice of
termination.
(2) If CMS’ initial determination to
terminate an ACO is reversed, the ACO
is reinstated into the Shared Savings
Program, retroactively back to the
original date of termination.
§ 425.16
Audits and record retention.
(a) Right to audit. The ACO must
agree, and must require its ACO
participants, ACO providers/suppliers,
and contracted entities performing
services or functions on behalf of the
ACO to agree, that the DHHS the
Comptroller General, the OIG or their
designees have the right to audit,
inspect, and evaluate any books,
contracts, records, documents and other
evidence of the ACO, ACO participants,
and ACO providers/suppliers, and other
contracted entities that pertain to—
(1) The ACO’s compliance with
program requirements;
(2) The quality of services performed
and determination of amount due to or
from CMS under the contract; and
(3) The ability of the ACO to bear the
risk of potential losses and to repay any
losses to CMS.
(b) Maintenance of records. An ACO
must agree, and must require its ACO
participants, ACO providers/suppliers,
and contracted entities performing
functions or services on behalf of the
ACO to agree to the following:
(1) To maintain and give DHHS, OIG,
the Comptroller General, or their
designees access to all books, contracts,
records, documents, and other evidence
(including data related to Medicare
utilization and costs, quality
performance measures, shared savings
distributions, and other financial
arrangements related to ACO activities)
sufficient to enable the audit,
evaluation, and inspection of the ACO’s
compliance with program requirements,
quality of services performed, right to
any shared savings payment, or
obligation to repay losses, ability to bear
the risk of potential losses, and ability
to repay any losses to CMS.
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(2) To maintain such books, contracts,
records, documents, and other evidence
for a period of 10 years from the final
date of the agreement period or from the
date of completion of any audit,
evaluation, or inspection, whichever is
later, unless—
(i) CMS determines there is a special
need to retain a particular record or
group of records for a longer period and
notifies the ACO at least 30 days before
the normal disposition date;
(ii) There has been a termination,
dispute, or allegation of fraud or similar
fault by the ACO, its ACO participants,
its ACO providers/suppliers, or
contracted entities that perform
functions or services on behalf of the
ACO, in which case ACOs must retain
records for an additional 6 years from
the date of any resulting final resolution
of the termination, dispute, or allegation
of fraud or similar fault.
(iii) There is a reasonable possibility
of fraud or similar fault by the ACO or
its participating providers/suppliers, or
contracted entities performing services
or functions on behalf of the ACO, in
which case CMS may inspect, evaluate,
and audit the ACO at any time.
(c) Notwithstanding any arrangements
between or among an ACO, ACO
participants, ACO providers/suppliers,
and contracted entities performing
functions or services on behalf of the
ACO, the ACO must have ultimate
responsibility for adhering to and
otherwise fully complying with all
terms and conditions of its agreement
with CMS, including the requirements
set forth in this section.
§ 425.17 Requirements for data
submission by ACOs.
(a) ACOs must submit data in a form
and manner specified by CMS on the
measures designated by CMS under
§ 425.9 of this part.
(b) ACOs that successfully must, on
behalf of their eligible professionals,
submit the measures designated by CMS
under § 425.9 according to the method
of submission established under the
Shared Savings Program for purposes of
the quality data requirements will be
considered satisfactory reporters for
purposes of the Physician Quality
Reporting System incentive under
§ 425.11(a).
§ 425.18
The 3-year agreement with CMS
(a) General rule. In order to
participate in the Shared Savings
Program, an ACO must enter into an
agreement with CMS. ACO applications
must be submitted by the deadline
established by CMS. CMS will
determine whether to approve or deny
applications from eligible organizations
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prior to the end of the calendar year in
which the applications are submitted.
(b) An ACO’s duration of agreement.
The participation agreement must be for
a term of 3 years, starting on the January
1 following approval of an application
or such other date specified in the
agreement.
(c) Performance period. Unless
otherwise specified, the ACO’s annual
performance period under the
agreement must be the 12-month period
beginning on January 1 of each year
during the term of the agreement.
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§ 425.19
Data sharing with ACOs.
(a) General rules. CMS shares both
aggregate and beneficiary identifiable
data with ACOs under the following
general conditions:
(1) The ACO does not unnecessary
limitations or restrictions on the use or
disclosure of individually identifiable
health information that it internally
compiles from providers and suppliers
both within and outside of the ACO.
(2) The ACO observes all relevant
statutory and regulatory provisions
regarding the appropriate use of data
and the confidentiality and privacy of
individually identifiable health
information and complies with the
terms of the data use agreement
described in paragraph (f) of this
section.
(b) Sharing aggregate data. (1) CMS
shares aggregate data (data that omits
the 18 identifiers listed at 45 CFR
164.514(b) with ACOs as follows:
(i) Aggregate data reports at the start
of the agreement period based on the
historical beneficiaries used to calculate
the benchmark, and each quarter
thereafter during the agreement period.
(ii) Quarterly reports will be based
upon the most recent 12 months of data
for beneficiaries that could potentially
be assigned to the ACO under the
assignment methodology in § 425.6.
These data will not include beneficiary
identifying information, but will
include de-identified claims history of
the services rendered for the ACO’s
assigned FFS beneficiaries, as
determined under § 425.6 of this part.
(2) These aggregate data reports will
include, when available, the following
information:
(i) Financial performance.
(ii) Quality performance scores.
(iii) Aggregated metrics on the
assigned beneficiary population.
(iv) Utilization data at the start of the
agreement period based on historical
beneficiaries used to calculate the
benchmark.
(c) Identification of historically
assigned beneficiaries used to calculate
the benchmark established under
§ 425.7.
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(1) At the beginning of the agreement
period, and at the end of each
performance period, CMS will, upon the
ACO’s request for the data for purposes
of population-based activities relating to
improving health or reducing health
care costs, protocol development, case
management, and care coordination,
provide the ACO the following data
about each beneficiary that was
included in the records used under
§ 425.7(a) and (b) of this part to generate
the ACO’s benchmark:
(i) Beneficiary names.
(ii) Date of birth.
(iii) HICN.
(2) In its request for these data, the
ACO must certify that it is seeking the
following information:
(i) As a HIPAA covered entity, and the
request reflects the minimum data
necessary for the ACO to conduct its
own health care operations work that
falls within the first or second
paragraph of the definition of health
care operations at 45 CFR 164.501.
(ii) As the business associate of its
ACO participants, who are HIPAA
covered entities, and the request reflects
the minimum data necessary for the
ACO to conduct health care operations
work that falls within the first or second
paragraph of the definition of health
care operations at 45 CFR 164.501 on
behalf of those participants.
(d) Sharing beneficiary identifiable
data. Subject to the opt-out described in
this paragraph (g) of this section, CMS
will, upon the ACO’s request for the
data for purposes of evaluating ACO
provider/supplier performance,
conducting quality assessment and
improvement activities, and conducting
population-based activities relating to
improved health, provide the ACO with
monthly claims data for potentially
assigned beneficiaries.
(1) If an ACO wishes to receive
beneficiary identifiable claims data, it
must either request these data as part of
the application process or later submit
a formal request for data.
(2) The ACO must certify that it is
requesting claims data about either of
the following:
(i) Its own patients, as a HIPAA
covered entity, and the request reflects
the minimum data necessary for the
ACO to conduct its own health care
operations work that falls within the
first or second paragraph of the
definition of health care operations at 45
CFR 164.501.
(ii) The patients of its HIPAA covered
entity ACO participants as the business
associate of these HIPAA covered
entities, and the request reflects the
minimum data necessary for the ACO to
conduct health care operations work
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Fmt 4701
Sfmt 4702
that falls within the first or second
paragraph of the definition of health
care operations at 45 CFR 164.501 on
behalf of those participants.
(3) The use of identifiers and claims
data will be limited to developing
processes and engaging in appropriate
activities related to coordinating care
and improving the quality and
efficiency of care that are applied
uniformly to all Medicare beneficiaries
assigned to the ACO, and that these data
will not be used to reduce, limit or
restrict care for specific beneficiaries.
(4) To ensure that beneficiaries have
a meaningful opportunity to opt-out of
having their claims data shared with the
ACO, the ACO may only request such
claims data about a beneficiary if—
(i) The beneficiary has been seen in
the office of a participating primary care
physician (as defined in § 425.4 of this
part), during the performance year,
(ii) The beneficiary was informed
about how the ACO intends to use
beneficiary identifiable claims data in
order to improve the quality of care that
is furnished to the beneficiary and,
where applicable, coordinate care
offered to the beneficiary; and
(iii) The beneficiary did not exercise
the opportunity to opt-out of having his/
her claims data shared with the ACO as
provided in paragraph (g) of the section.
(5) CMS will continue to provide
ACOs with certain beneficiary
identifiable claims data on a monthly
basis, subject to beneficiary’s
opportunity to opt-out of the data
sharing under paragraph (g) of this
section.
(6) If an ACO requests beneficiary
identifiable information, compliance
with the terms of the data use agreement
described in paragraph (f) of this section
is a condition of an ACO’s participation
in the Shared Savings Program.
(e) Minimum necessary data set. (1)
The minimum necessary Parts A and B
data elements may include the
following data elements:
(i) Beneficiary ID.
(ii) Date of birth.
(iii) Gender.
(iv) Date of death.
(v) Claim ID.
(vi) The from and through dates of
service.
(vii) The provider or supplier ID.
(viii) The claim payment type.
(2) The minimum necessary Part D
data elements may include the
following data elements:
(i) Beneficiary ID.
(ii) Prescriber ID.
(iii) Drug service date.
(iv) Drug product service ID.
(v) Quantity dispensed.
(vi) Days supplied.
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(vii) Gross drug cost.
(viii) Brand name.
(ix) Generic name.
(x) Drug strength.
(xi) Indication if the drug is on the
formulary, as designated by CMS.
(f) Data Use Agreement. Prior to
receiving any beneficiary identifiable
data, ACOs must enter into a DUA with
CMS. The DUA must—
(1) Specify that the ACO will comply
with the limitations on the use and
disclosure of individually identifiable
health information that the HIPAA
Privacy Rule places on HIPAA covered
entities, as well as all other applicable
privacy and confidentiality
requirements;
(2) Prohibit the ACO from using the
data received under the Shared Savings
Program for any prohibited use of
individually identifiable health
information.
(3) Specify that if an ACO misuses or
discloses data in a manner that violates
any applicable statutory or regulatory
requirements or that is otherwise noncompliant with the provisions of the
DUA, it will no longer be eligible to
receive data, could potentially be
terminated from the shared savings
program as well as subject to additional
sanctions and penalties available under
the law.
(g) Beneficiary opportunity to opt-out
of claims data sharing. (1) Prior to
requesting claims data about a particular
beneficiary, the ACO must inform the
beneficiary that it may request personal
health information about the beneficiary
for purposes of its care coordination and
quality improvement work, and give the
beneficiary meaningful opportunity to
opt-out of having his/her claims
information shared with the ACO.
(2) The ACO must supply
beneficiaries with a form allowing them
to opt-out of data sharing. The form
must be provided to each beneficiary as
part of an office visit with a primary
care physician as defined under § 425.4,
whose services are used to assign
beneficiaries to the ACO.
(3) This requirement will not apply to
the initial four data points that CMS
will provide to ACOs for individuals in
the 3-year base data set (Beneficiary
Name, Beneficiary DOB, Beneficiary
Sex, and Beneficiary HICN) under
paragraph (c) of this section.
§ 425.20 New program standards
established during the 3 year agreement
period.
(a)(1) ACOs will be subject to all
statutory changes.
(2) ACOs will be subject to all
regulatory changes with the exception of
the following program areas:
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19:58 Apr 06, 2011
Jkt 223001
(i) Eligibility requirements concerning
the structure and governance of ACOs.
(ii) Calculation of sharing rate.
(iii) Beneficiary assignment.
(b) In those instances where changes
in law or regulations require, or
otherwise cause an ACO to change its
processes in a manner that affects the
design of its care processes and delivery
of care, changes to the quality of care,
or changes in planned distribution of
shared savings, the ACO will be
required to submit to CMS for review
and approval a supplement to its
original application detailing how it
will address key changes in processes
resulting from these modifications.
(c) If an ACO cannot effectuate the
changes needed to adhere to the
regulatory modifications after being
given an opportunity to act upon a CAP,
the ACO would be terminated from the
program.
(d) Nothing in the regulations under
this part shall be construed to affect the
payment, coverage, program integrity,
and other requirements that apply to
providers and suppliers under FFS
Medicare.
§ 425.21 Managing significant changes to
the ACO during the agreement period.
(a)(1) During the 3-year agreement, an
ACO may remove, but not add, ACO
participants (identified by TINs), and it
may remove or add ACO providers/
suppliers (identified by NPI and/or
TIN).
(2) ACOs must notify CMS at least 30
days prior to any significant change, as
defined in paragraph (b).
(3) CMS will review the ACO’s
notification and make one of the
following determinations:
(i) The ACO may continue to operate
under the new structure with savings
calculations for the performance year
based upon the updated list of ACO
participant TINs.
(ii) The ACO structure is so different
from the initially approved ACO that it
must submit a new application, and, if
applicable, undergo an antitrust review.
(iii) The ACO is materially different
from the initially approved ACO
because of the inclusion of additional
ACO providers/suppliers such that, in
order to continue in the program, the
ACO must obtain an antitrust review
and a letter from the reviewing Antitrust
Agency stating that it has no present
intent to challenge, or to recommend
challenging, the ACO. An ACO’s failure
to timely request antitrust review shall
be deemed to constitute voluntary
termination of its 3-year agreement.
(iv) The ACO no longer meets the
eligibility criteria for the program and
its 3-year agreement must be terminated.
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Frm 00127
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19653
(v) CMS and the ACO may mutually
decide to terminate the agreement.
(b) A ‘‘significant change’’ occurs
when an ACO is unable to fulfill its 3year agreement due to:
(i) Deviation from its approved
application such as a reorganization of
the ACO’s legal structure or other
changes in eligibility.
(ii) A material change as defined in
§ 425.14.
(iii) Government-required
reorganization as a result of fraud or
antitrust concerns.
(c) The ACO must notify CMS within
30 days of the event for reevaluation of
its eligibility to continue to participate
in the Shared Savings Program.
(d) ACO participants continue to be
subject to all requirements applicable to
fee-for-service Medicare, including
routine CMS business operation
updates, and changes in fee-for-service
coverage decisions.
§ 425.22 Future participation of previous
Shared Savings Program participants.
(a) The ACO must disclose to CMS
whether the ACO, its ACO participants,
or its ACO providers/suppliers have
participated in the Medicare program
under the same or a different name, or
is related to or has an affiliation with
another Shared Savings Program ACO.
The ACO must specify whether the
related ACO was terminated or
withdrew voluntarily from the program.
(b) If the ACO was previously
terminated from the program, the
applicant must identify the cause of
termination and what safeguards are
now in place to enable the applicant
ACO to participate in the program for
the full of the three-year agreement
period. For new ACOs, this should be
disclosed on a prospective ACO’s
application. For ACOs that are already
participating in the Shared Savings
Program, this information should be
included in the annual updates that the
ACOs will provide to CMS on their ACO
participants and ACO providers/
suppliers.
§ 425.23 Public reporting and
transparency.
For purposes of the shared savings
program, each ACO will publicly report
the following information regarding the
ACO a standardized format specified by
CMS:
(a) Name and location.
(b) Primary contact.
(c) Organizational information
including all of the following:
(1) Participating providers of services
and suppliers.
(2) Identification of participants in
joint ventures between ACO
professionals and hospitals.
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(3) Identification of the
representatives on its governing body.
(4) Associated committees and
committee leadership.
(5) Quality performance standard
scores.
(d) Shared savings or losses
information, including the amount of
any shared savings performance
payment received by the ACOs or
shared losses owed to CMS.
(e) Total proportion of shared savings
that was distributed among ACO
participants and total proportion that
was used to support quality
performance and the aims of better care
for individuals, better health for
populations, and lower growth in
expenditures.
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§ 425.24 Overlap with other CMS Shared
Savings initiatives.
(a) Medicare providers and suppliers
may not participate in the Shared
Savings Program as ACO participants if
they participate in the independence at
home medical practice pilot program
under section 1866E of the Act, a model
tested or expanded under section 1115A
of the Act that involves shared savings,
or any other Medicare initiative that
involves shared savings. CMS will
review and reject an ACO’s application
if ACO participants are participating in
another Medicare initiative that
involves shared savings payments so
that beneficiaries are assigned to only
one such initiative and in order to avoid
duplicate shared savings payments.
PO 00000
Frm 00128
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(b) PGP demonstration sites applying
for participation to the Shared Savings
Program will be required to complete a
condensed application form.
(Catalog of Federal Domestic Assistance
Program No. 93.773, Medicare—Hospital
Insurance; and Program No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
Dated: March 24, 2011.
Donald M. Berwick,
Administrator, Centers for Medicare &
Medicaid Services.
Approved: March 29, 2011.
Kathleen Sebelius,
Secretary.
[FR Doc. 2011–7880 Filed 3–31–11; 11:15 am]
BILLING CODE 4120–01–P
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Agencies
[Federal Register Volume 76, Number 67 (Thursday, April 7, 2011)]
[Proposed Rules]
[Pages 19528-19654]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-7880]
[[Page 19527]]
Vol. 76
Thursday,
No. 67
April 7, 2011
Part II
Department of Health and Human Services
-----------------------------------------------------------------------
Centers for Medicare & Medicaid Services
Office of the Inspector General
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42 CFR Part 425
Medicare Program; Medicare Shared Savings Program: Accountable Care
Organizations and Medicare Program: Waiver Designs in Connection With
the Medicare Shared Savings Program and the Innovation Center; Proposed
Rule and Notice
Federal Register / Vol. 76, No. 67 / Thursday, April 7, 2011 /
Proposed Rules
[[Page 19528]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 425
[CMS-1345-P]
RIN 0938-AQ22
Medicare Program; Medicare Shared Savings Program: Accountable
Care Organizations
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: This proposed rule would implement section 3022 of the
Affordable Care Act which contains provisions relating to Medicare
payments to providers of services and suppliers participating in
Accountable Care Organizations (ACOs). Under these provisions,
providers of services and suppliers can continue to receive traditional
Medicare fee-for-service payments under Parts A and B, and be eligible
for additional payments based on meeting specified quality and savings
requirements.
DATES: To be assured consideration, comments must be received at one of
the addresses provided below, no later than 5 p.m. on June 6, 2011.
ADDRESSES: In commenting, please refer to file code CMS-1345-P. 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
regulation 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-1345-P, 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-1345-P, Mail
Stop C4-26-05, 7500 Security Boulevard, Baltimore, MD 21244-1850.
4. By hand or courier. If you prefer, you may deliver (by hand or
courier) your written comments before the close of the comment period
to either of 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,
please call telephone number (410) 786-7195 in advance to schedule your
arrival with one of our staff members.
Comments mailed to the addresses indicated as appropriate for hand
or courier delivery may be delayed and received after the comment
period.
Submission of comments on paperwork requirements. You may submit
comments on this document's paperwork requirements by following the
instructions at the end of the ``Collection of Information
Requirements'' section in this document.
For information on viewing public comments, see the beginning of
the SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Dr. Terri Postma (410)786-8084.
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 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. To schedule an appointment to view public comments,
phone 1-800-743-3951.
Table of Contents
To assist readers in referencing sections contained in this
preamble, we are providing a table of contents.
I. Background
A. Introduction and Overview of Value-Based Purchasing
B. Statutory Basis for the Medicare Shared Savings Program
C. Overview and Intent of the Medicare Shared Savings Program
D. Related Affordable Care Act Provisions
1. Establishment of Center for Medicare and Medicaid Innovation
(Innovation Center)
2. Independence at Home Medical Practices
3. State Option To Provide Health Homes
4. Community Health Teams
E. Related Ongoing CMS Efforts
1. Physician Group Practice Demonstration
2. Medicare Health Care Quality Demonstration
II. Provisions of the Proposed Rule
A. Organizations of the Proposed Rule
B. Eligibility and Governance
1. Eligible Entities
2. Legal Structure and Governance
a. Legal Entity
b. Governance
c. Composition of the Governing Body
3. Leadership and Management Structure
4. Accountability for Beneficiaries
5. Agreement Requirement
6. Distribution of Savings
7. Sufficient Number of Primary Care Providers and Beneficiaries
8. Required Reporting on Participating ACO Professionals
9. Processes To Promote Evidence-Based Medicine, Patient
Engagement, Reporting, and Coordination of Care
a. Processes To Promote Evidence-Based Medicine
b. Processes To Promote Patient Engagement
c. Processes To Report on Quality and Cost Measures
d. Processes To Promote Coordination of Care
10. Patient Centeredness Criteria
a. Beneficiary Experience of Care Survey
b. Patient Involvement in Governance
c. Evaluation of Population Health Needs and Consideration of
Diversity
d. Implementation of Individualize Care Plans and Integration of
Community Resources
11. ACO Marketing Guidelines
12. Program Integrity Requirements
a. Compliance Plans
b. Compliance With Program Requirements
c. Conflicts of Interest
d. Screening of ACO Applicants
e. Prohibition on Certain Required Referrals and Cost Shifting
C. Establishing the 3-YearAgreement With the Secretary
[[Page 19529]]
1. Options for Start Date of the Performance Year
2. Timing and Process for Evaluating Shared Savings
3. Data Sharing
4. Sharing Aggregate Data
5. Identification of Historically Assigned Beneficiaries
6. Sharing Beneficiary Identifiable Claims Data
a. Legal Authority To Provide Beneficiary Identifiable Data to
ACOs
(1) Sharing Data Related to Medicare Parts A and B
(2) Sharing Data Related to Medicare Part D
b. Beneficiary Opportunity To Opt Out of Claims Data Sharing
7. New Program Standards Established During 3-Year Agreement
Period
8. Managing Significant Changes to the ACO During the Agreement
Period
9. Future Participation of Previously Terminated Program
Participants
D. Assignment of Medicare Fee-For-Service Beneficiaries
1. Operational Identification of an ACO
2. Definition of Primary Care Services
3. Prospective vs. Retrospective Beneficiary Assignment to
Calculate Eligibility for Shared Savings
4. Majority vs. Plurality Rule for Beneficiary Assignment
5. Beneficiary Information and Notification
E. Quality and Other Reporting Requirements
1. Introduction
2. Proposed Measures To Assess the Quality of Care Furnished by
an ACO
a. General
b. Considerations in Selecting Measures
1. Use of Measures
2. Scoring Methodology
c. Proposed Quality Measures for Use in Establishing Quality
Performance Standards that ACOs Must Meet for Shared Savings
3. Requirements for Quality Measures Data Submission by ACOs
a. General
b. GPRO Tool
c. Certified EHR Technology
4. Quality Performance Standards
a. General
b. Option 1--Performance Scoring
(1) Measure Domains and Measures Included in the Domains
(2) Methodology for Calculating a Performance Score for Each
Measure Within a Domain
(3) Methodology for Calculating a Performance Score for Each
Domain
(4) The Quality Performance Standard Level
c. Option 2--Quality Threshold
(1) Minimum Quality Threshold
(2) Considerations in Establishing a Quality Threshold
5. Incorporation of Other Reporting Requirements Related to the
Physician Quality Reporting System and Electronic Health Records
Technology Under Section 1848 of the Act
6. Public Reporting
7. Aligning ACO Quality Measures with other Laws and Regulations
F. Shared Savings Determination
1. Background
2. Overview of Shared Savings Determination
3. Establishing an Expenditure Benchmark
a. Background
b. Option 1
c. Option 2
d. Summary
4. Adjusting the Benchmark and Average Per Capita Expenditures
for Beneficiary Characteristics
5. Technical Adjustments to the Benchmark Impact of IME and DSH
6. Technical Adjustments to the Benchmark Impact of Geographic
Payment Adjustments on the Calculation of the Benchmark
7. Technical Adjustments to the Benchmark Impact of Bonus
Payments and Penalties on the Calculation of the Benchmark and
Actual Expenditures
8. Trending Forward Prior Years' Experience To Obtain an Initial
Benchmark
a. Flat Dollar vs Growth Rate as a Benchmark Trending Factor
b. National vs Local Growth Rate as a Benchmark Trending Factor
9. Updating the Benchmark During the Agreement Period
10. Minimum Savings Rate (MSR) and Sharing Rate
11. Net Sharing Rate
12. Additional Shared Savings Payments
13. Withholding Performance Payments To Offset Future Losses
14. Performance Payment Limit
G. Two-Sided Model
1. Risk-Based Payment Models
2. Two Tracks Provide Incremental Approach to Incorporating Risk
3. Elements of the Two-Sided Model
a. Beneficiary Notification and Protections
b. Eligibility Requirements
c. Quality Performance Measurement and Scoring
d. Shared Savings Methodology
(1) Minimum Savings Rate
(2) Additional Shared Savings Payments
(3) Net Sharing Rate
(4) Calculating Sharing in Losses
(5) Maximum Shared Savings and Shared Loss Caps
e. Ensuring ACO Repayment of Shared Losses
f. Future Participation of Under-performing Organizations
g. Public Reporting
h. Impact on States
4. Verification of Savings and Losses
H. Monitoring and Termination of ACOs
1. Monitoring Avoidance of At Risk Beneficiaries
2. Monitoring Compliance with Quality Performance Standards
3. Terminating an ACO Agreement
4. Reconsideration Review Process
I. Coordination With Other Agencies
1. Waivers of CMP, Anti Kickback, and Physician Self Referral
Laws
2. IRS Guidance Relating to Tax Exempt Organization
3. Antitrust Policy Statement
4. Prohibition Against the Shared Savings Program Participation
by ACOs With Market Power
a. Coordinating the Shared Savings Program Application With the
Antitrust Agencies
b. Competition and Quality of Care
c. Competition, Price, and Access to Care
J. Overlap With Other CMS Shared Savings Initiatives
1. Duplication in Participation in Medicare Shared Savings
Programs
2. Transition of the Physician Group Practice (PGP)
Demonstration Sites Into the Shared Savings Program
3. Overlap With the Center for Medicare & Medicaid Innovation
(Innovation Center Shared Savings Models
III. Collection of Information Requirements
IV. Response to Comments
V. Regulatory Impact Analysis
A. Introduction
B. Statement of Need
C. Anticipated Effects
1. Effects on the Medicare Program
a. Assumptions and Uncertainties
b. Detailed Stochastic Modeling Results
c. Further Considerations
2. Impact on Beneficiaries
3. Impact on Providers and Suppliers
D. Alternatives Considered
E. Accounting Statement and Table
F. Conclusion
Acronyms
ACO Accountable Care Organizations
AHRQ Agency for Healthcare Research and Quality
BCBSMA Blue Cross Blue Shield of Massachusetts
BIPA Benefits Improvement and Protection Act
BQI Better Quality Information
CAD Coronary Artery Disease
CAHPS Consumer Assessment of Health Providers and Systems
CAHs Critical Access Hospitals
CAM Complementary and Alternative Services
CBIC Competitive Bidding Implementation Contractor
CCNC Community Care of North Carolina
CHCs Community Health Centers
CHIP Children's Health Insurance Program
CMMI Center for Medicare and Medicaid Innovation
CMP Civil Monetary Penalties
CMS Centers for Medicare and Medicaid Services
CNM Certified Nurse Midwife
CMS-HCC CMS Hierarchal Condition Category
COPD Chronic Obstructive Pulmonary Disease
CP Certified Psychologist
CSW Clinical Social Worker
CVE Chartered Value Exchange
CWF Common Working File
DHHS Department of Health and Human Services
DM Diabetes Mellitus
DOJ Department of Justice
DRA Deficit Reduction Act of 2005(Pub. L. 109-171)
DSH Disproportionate Share Hospital
DUA Data use Agreement
E&M Evaluation and Management
EDB Enrollment Database
EHR Electronic Health Record
[[Page 19530]]
ESRD End Stage Renal Disease
eRx Electronic Prescribing Incentive Program
FFS Fee For Service
FQHCs Federally Qualified Health Centers
FTC Federal Trade Commission
GAO Government Accountability Office
GPCI Geographic Practice Cost Index
GPRO Group Practice Reporting Option
HAC Hospital Acquired Conditions
HCAHPS Health Care Providers Systems and Surveys
HCC Hierarchal Condition Category
HCO Health Care Organizations
HCPCS Health Care Procedural Coding System
HHA Home Health Agencies
HICN Health Insurance Claim Number
HIPAA Heath Insurance Portability and Accountability Act of 1996
HIE Health Information Exchange
HIT Health Information Technology
HITECH Health Information Technology for Economic and Clinical
Health
HMO Health Maintenance Organization
HRSA Health Resources Services Administration
HVBP Hospital Value Based Purchasing
IHIE Indiana Health Information Exchange
IME Indirect Medical Education
INPC Indiana Network for Patient Care
IOM Institute of Medicine
IPPS Inpatient Prospective Payment System
IQR Inpatient Quality Reporting
IRS Internal Revenue Services
LTCHs Long-Term Acute Care Hospitals
MA Medicare Advantage
MAeHC Massachusetts eHealth Collaborative
MDCs Major Diagnostic Categories
MedPAC Medicare Payment Advisory Commission
MHCQ Medicare Health Care Quality
MMA Medicare Prescription Drug, Improvement, and Modernization Act
MPFS Medicare Physician Fee Schedule
MS-DRGs Medicare Severity-Diagnosis Related Groups
MSP Minimum Savings Percentage
MSR Minimum Savings Rate
NC-CCN North Carolina Community Care Networks
NCH National Claims History
NCQA National Committee for Quality Assurance
NP Nurse Practitioner
NPI National Provider Identifier
NQF National Quality Forum
NYCLIX The New York Clinical Information Exchange
OIG Office of Inspector General
OMB Office of Management and Budget
PA Physician Assistant
PACE Program of All Inclusive Care for the Elderly
PACFs Post-Acute Care Facilities
PCMH Patient Centered Medical Home
PFS Physician Fee Schedule
PGP Physician Group Practice
PHI Protected health information
POS Point of Service
PPO Preferred provider organization
PPS Prospective Payment System
PQRI Physician Quality Reporting Initiative
PQRS Physician Quality Reporting System
PRA Paperwork Reduction Act
PSA Primary Service Areas
RFI Request for Information
RHCs Rural Health Centers
RHQDAPU Reporting Hospital Quality Data for Annual Payment Update
RIA Regulatory Impact Analysis
SNFs Skilled Nursing Facilities
SOR Privacy Act Systems of Record
SSA Social Security Administration
SSN Social Security Number
TIN Tax Identification Number
I. Background
A. Introduction and Overview of Value-Based Purchasing
On March 23, 2010, the Patient Protection and Affordable Care Act
(Pub. L. 111-148) was enacted. Following the enactment of Public Law
111-148, the Health Care and Education Reconciliation Act of 2010 (Pub.
L. 111-152) (enacted on March 30, 2010), amended certain provisions of
Public Law 111-148. These public laws are collectively known as the
Affordable Care Act. The Affordable Care Act includes a number of
provisions designed to improve the quality of Medicare services,
support innovation and the establishment of new payment models in the
program, better align Medicare payments with provider costs, strengthen
program integrity within Medicare, and put Medicare on a firmer
financial footing.
With respect to quality improvement, the Affordable Care Act
includes provisions to expand value-based purchasing, broaden quality
reporting, improve the level of performance feedback available to
suppliers, create incentives to enhance quality, improve beneficiary
outcomes, and increase the value of care.
Value-based purchasing is a concept that links payment directly to
the quality of care provided and is a strategy that can help transform
the current payment system by rewarding providers for delivering high
quality, efficient clinical care. We have significant experience in
developing, refining, and expanding health care quality performance
measures through our experience with value-based demonstration efforts,
noting some of these efforts later in the document, and various
Medicare payment systems. For example, since 2005, we have applied the
Hospital Inpatient Quality Reporting (IQR) Program under the hospital
inpatient prospective payment system. Hospital IQR provides
differential payments to hospitals that meet certain requirements,
including publicly reporting their performance on a defined set of
inpatient care performance measures. Beginning in 2007, under the
physician fee schedule, we have provided for quality measure reporting
through the Physician Quality Reporting System, which includes
incentive payments for eligible professionals who satisfactorily report
data on quality measures for covered professional services furnished to
Medicare beneficiaries. In 2009, Congress passed the Health Information
and Technology for Economic and Clinical Health (HITECH) Act. As part
of the Electronic Health Records (EHR) Incentive Program under HITECH,
we have defined measures for the meaningful use of certified electronic
health records technology and have developed incentive payment programs
for both Medicare and Medicaid providers. We have extended similar
efforts to additional payment systems, including the hospital
outpatient prospective payment system and various post-acute care
systems.
In addition to improving quality, value-based purchasing
initiatives seek to reduce growth in health care expenditures. It is
widely recognized that the trajectory for the nation's health care
spending is unsustainable. Medicare beneficiaries share in the burden
of rising costs, as they pay higher premiums, and larger cost-sharing
obligations and out-of-pocket expenses. The Affordable Care Act
includes a series of reforms expected to significantly slow growth in
the Medicare spending rate while simultaneously strengthening the care
provided to Medicare beneficiaries. These reforms build upon existing
value-based purchasing efforts currently underway within CMS to find
ways to better coordinate care and reduce unnecessary services to lower
the growth in Medicare spending while improving the quality of care
received by beneficiaries.
We view value-based purchasing as an important step to revamping
how care and services are paid for, moving increasingly toward
rewarding better value, outcomes, and innovations instead of merely
volume. In implementing these value-based purchasing initiatives, we
seek to meet certain common goals, as follows:
Improving quality.
++ Value-based payment systems and public reporting should rely on
a mix of standards, processes, outcomes, and patient experience
measures, including measures of care transitions and changes in patient
functional status. Across all programs, we seek to move as quickly as
possible to the use of outcome and patient experience measures. To the
extent practicable and appropriate, these outcome and patient
experience measures should be adjusted
[[Page 19531]]
for risk or other appropriate patient, population, or provider
characteristics.
++ To the extent possible, and recognizing differences in payment
system readiness and statutory authorities, measures should be aligned
across Medicare and Medicaid's public reporting and payment systems. We
seek to evolve a focused core-set of measures appropriate to each
specific provider category that reflects the level of care and the most
important areas of service and measures for that provider.
++ The collection of information should minimize the burden on
providers to the extent possible. As part of that effort, we will
continuously seek to align our measures with the adoption of meaningful
use standards for health information technology (HIT), so the
collection of performance information is part of care delivery.
++ To the extent practicable, the measures used by the Shared
Savings Program should be nationally endorsed by a multistakeholder
organization. We should align measures with best practices among other
payers and the needs of the end users of the measures.
Lowering growth in expenditures.
++ Providers should be accountable for the cost of care, and be
rewarded for reducing unnecessary expenditures and be responsible for
excess expenditures.
++ In reducing excess expenditures, providers should continually
improve the quality of care they deliver and must honor their
commitment to do no harm to beneficiaries.
++ To the extent possible, and recognizing differences in payers'
value-based purchasing initiatives, providers should apply cost
reducing and quality improving redesigned care processes to their
entire patient population.
As noted previously, the Affordable Care Act includes provisions to
expand value-based purchasing, broaden quality reporting, improve the
level of performance feedback available to suppliers, create incentives
to enhance quality, improve beneficiary outcomes, and increase the
value of care. Among these provisions, section 3022 of the Affordable
Care Act requires the Secretary to establish the Medicare Shared
Savings Program (Shared Savings Program), intended to encourage the
development of Accountable Care Organizations (ACOs) in Medicare. The
Affordable Care Act intends the Medicare Shared Saving Program to be a
program ``that promotes accountability for a patient population and
coordinates items and services under parts A and B, and encourages
investment in infrastructure and redesigned care processes for high
quality and efficient service delivery.'' The Shared Savings Program is
a key Medicare delivery system reform initiatives that will be
implemented under the Affordable Care Act and is a new approach to the
delivery of health care aimed at: (1) Better care for individuals; (2)
better health for populations; and (3) lower growth in expenditures. We
refer to this approach throughout the document as the three-part aim.
B. Statutory Basis for the Medicare Shared Savings Program
Section 3022 of the Affordable Care Act amended Title XVIII of the
Social Security Act (the Act) (42 U.S.C. 1395 et seq.) by adding new
section 1899 to the Act to establish a Shared Savings Program that
promotes accountability for a patient population, coordinates items and
services under Parts A and B, and encourages investment in
infrastructure and redesigned care processes for high quality and
efficient service delivery. Section 1899(a)(1) of the Act requires the
Secretary to establish this program no later than January 1, 2012.
Section 1899(a)(1)(A) of the Act further provides that, ``groups of
providers of services and suppliers meeting criteria specified by the
Secretary may work together to manage and coordinate care for Medicare
fee-for-service beneficiaries through an [ACO]''. Section 1899(a)(1)(B)
of the Act also provides that ACOs that meet quality performance
standards established by the Secretary are eligible to receive payments
for ``shared savings''.
Section 1899(b)(1) of the Act establishes the types of groups of
providers of services and suppliers, with established mechanisms for
shared governance, that are eligible to participate as ACOs under the
program, subject to the succeeding provisions of section 1899 of the
Act, as determined appropriate by the Secretary. Specifically, sections
1899(b)(1)(A) through (E) of the Act provide, respectively, that the
following groups of providers of services and suppliers are eligible to
participate:
ACO professionals in group practice arrangements.
Networks of individual practices of ACO professionals.
Partnerships or joint venture arrangements between
hospitals and ACO professionals.
Hospitals employing ACO professionals.
Such other groups of providers of services and suppliers
as the Secretary determines appropriate.
Section 1899(b)(2) of the Act establishes the requirements that
such eligible groups must meet in order to participate in the program.
Specifically, sections 1899(b)(2)(A) through (H) of the Act provide,
respectively, that eligible groups of providers of services and
suppliers must meet the following requirements to participate in the
program as ACOs:
The ACO shall be willing to become accountable for the
quality, cost, and overall care of the Medicare fee-for-service (FFS)
beneficiaries assigned to it.
The ACO shall enter into an agreement with the Secretary
to participate in the program for not less than a 3-year period.
The ACO shall have a formal legal structure that would
allow the organization to receive and distribute payments for shared
savings to participating providers of services and suppliers.
The ACO shall include primary care ACO professionals that
are sufficient for the number of Medicare FFS beneficiaries assigned to
the ACO. At a minimum, the ACO shall have at least 5,000 such
beneficiaries assigned to it in order to be eligible to participate in
the Shared Savings Program.
The ACO shall provide the Secretary with such information
regarding ACO professionals participating in the ACO as the Secretary
determines necessary to support the assignment of Medicare fee-for-
service beneficiaries to an ACO, the implementation of quality and
other reporting requirements, and the determination of payments for
shared savings.
The ACO shall have in place a leadership and management
structure that includes clinical and administrative systems.
The ACO shall define processes to promote evidence-based
medicine and patient engagement, report on quality and cost measures,
and coordinate care, such as through the use of telehealth, remote
patient monitoring, and other such enabling technologies.
The ACO shall demonstrate to the Secretary that it meets
patient-centeredness criteria specified by the Secretary, such as the
use of patient and caregiver assessments or the use of individualized
care plans.
Section 1899(b)(3) of the Act establishes the quality and other
reporting requirements for the Shared Savings Program. For purposes of
quality reporting, section 1899(b)(3)(A) of the Act provides that the
Secretary shall determine appropriate measures to assess the quality of
care furnished by the ACO, such as measures of clinical processes and
outcomes, patient and,
[[Page 19532]]
where practicable, caregiver experience of care, and utilization (such
as rates of hospital admissions for ambulatory care sensitive
conditions). Section 1899(b)(3)(B) of the Act requires an ACO to submit
data in a form and manner specified by the Secretary on measures the
Secretary determines necessary for the ACO to report in order to
evaluate the quality of care furnished by the ACO. This provision
further states that such data may include care transitions across
health care settings, including hospital discharge planning and post-
hospital discharge follow-up by ACO professionals, as determined to be
appropriate by the Secretary. Section 1899(b)(3)(C) of the Act requires
the Secretary to establish quality performance standards to assess the
quality of care furnished by ACOs. That section also requires that the
Secretary shall seek to improve the quality of care furnished by ACOs
over time by specifying higher standards, new measures, or both for
purposes of assessing such quality of care. Finally, section
1899(b)(3)(D) of the Act provides that the Secretary may, as the
Secretary determines appropriate, incorporate reporting requirements
and incentive payments related to the Physician Quality Reporting
System under section 1848 of the Act, including such requirements and
such payments related to electronic prescribing, electronic health
records, and other similar initiatives under section 1848 of the Act,
and may use alternative criteria than would otherwise apply under such
section for determining whether to make such payments. CMS should not
take the incentive payments described in the preceding sentence into
consideration when calculating any payments otherwise made under of
section 1899(d) the Act.
Section 1899(b)(4) of the Act prohibits duplication in
participation in other shared savings programs by participants in the
Shared Savings Program. Specifically, a provider of services or
supplier that participates in any of the following is not eligible to
participate in an ACO under the Shared Savings Program: A model tested
or expanded under section 1115A of the Act that involves shared savings
under this title, any other program or demonstration project that
involves such shared savings, or the Independence at Home Demonstration
under section 1866E of the Act.
Section 1899(c) of the Act provides the Secretary with discretion
to determine an appropriate method to assign Medicare FFS beneficiaries
to an ACO participating in the Shared Savings Program. This discretion
is limited, however, by the fact that under the Act, assignment must be
based on beneficiaries' utilization of primary care services provided
under Medicare by an ACO professional who is a physician as defined in
section 1861(r)(1) of the Act.
Section 1899(d) of the Act establishes the principles and
requirements for payments and treatment of savings under the Shared
Savings Program. Specifically, section 1899(d)(1)(A) of the Act
provides that, subject to the requirements concerning monitoring
avoidance of at-risk patients, payments shall continue to be made to
providers of services and suppliers participating in an ACO under the
original Medicare FFS program under Parts A and B in the same manner as
they would otherwise be made, except that a participating ACO is
eligible to receive payment for shared savings if the following occur:
The ACO meets quality performance standards established by
the Secretary; and
The ACO meets the requirements for realizing savings.
Section 1899(d)(1)(B) of the Act establishes the savings
requirements and the method for establishing and updating the benchmark
against which any savings would be determined. Specifically, section
1899(d)(1)(B)(i) of the Act establishes that, in each year of the
agreement period, an ACO shall be eligible to receive payment for
shared savings only if the estimated average per capita Medicare
expenditures under the ACO for Medicare FFS beneficiaries for Parts A
and B services, adjusted for beneficiary characteristics, is at least
the percent specified by the Secretary below the applicable benchmark.
The Secretary shall determine the appropriate percent of shared savings
to account for normal variation in Medicare expenditures, based upon
the number of Medicare FFS beneficiaries assigned to an ACO. Section
1899(d)(1)(B)(ii) of the Act, in turn, requires the Secretary to
estimate a benchmark for each agreement period for each ACO using the
most recent available 3 years of per beneficiary expenditures for Parts
A and B services for Medicare FFS beneficiaries assigned to the ACO.
This benchmark must be adjusted for beneficiary characteristics and
such other factors as the Secretary determines appropriate and updated
by the projected absolute amount of growth in national per capita
expenditures for Parts A and B services under the original Medicare FFS
program, as estimated by the Secretary. Furthermore, the benchmark must
be reset at the start of each new agreement period.
Section 1899(d)(2) of the Act provides for the actual payments for
shared savings under the Shared Savings Program. Specifically, if an
ACO meets the quality performance standards established by the
Secretary, and meets the savings requirements, a percent (as determined
appropriate by the Secretary) of the difference between the estimated
average per capita Medicare expenditures in the year, adjusted for
beneficiary characteristics, and the benchmark for the ACO may be paid
to the ACO as shared savings and the remainder of the difference shall
be retained by the Medicare program. The Secretary is required to
establish limits on the total amount of shared savings paid to an ACO.
Section 1899(d)(3) of the Act requires the Secretary to monitor
ACOs for avoidance of at-risk patients. Specifically, if the Secretary
determines that an ACO has taken steps to avoid patients at risk in
order to reduce the likelihood of increasing costs to the ACO, the
Secretary may impose an appropriate sanction on the ACO, including
termination from the program. Section 1899(d)(4) of the Act, in turn,
provides that the Secretary may terminate an agreement with an ACO if
it does not meet the quality performance standards established by the
Secretary. Section 1899(e) of the Act provides that chapter 35 of title
44 of the U.S. Code, which includes such provisions as the Paperwork
Reduction Act (PRA), shall not apply to the Shared Savings Program.
Section 1899(f) of the Act further provides the Secretary with the
authority to waive such requirements of sections 1128A and 1128B of the
Act and title XVIII of the Act as may be necessary to carry out the
Shared Savings Program. Section 1899(g) of the Act establishes
limitations on judicial and administrative review of the Shared Savings
Program. This section provides that there shall be no administrative or
judicial review under section 1869 of the Act, section 1878 of the Act,
or otherwise of the following:
The specification of criteria under 1899(a)(1)(B) of the
Act.
The assessment of the quality of care furnished by an ACO
and the establishment of performance standards under 1899(b)(3) of the
Act.
The assignment of Medicare FFS beneficiaries to an ACO
under 1899(c) of the Act.
The determination of whether an ACO is eligible for shared
savings under 1899(d)(2) of the Act and the amount of such shared
savings, including the determination of the estimated average per
capita Medicare expenditures under the ACO for Medicare FFS
beneficiaries
[[Page 19533]]
assigned to the ACO and the average benchmark for the ACO under
1899(d)(1)(B) of the Act.
The percent of shared savings specified by the Secretary
under 1899(d)(2) of the Act and any limit on the total amount of shared
savings established by the Secretary under such subsection.
The termination of an ACO under 1899(d)(4) of the Act for
failure to meet the quality performance standards.
Section 1899(h) of the Act defines some basic terminology that
applies to the Shared Savings Program. Specifically, section 1899(h)(1)
of the Act defines the term ``ACO professional'' as a physician (as
defined in section 1861(r)(1) of the Act) or a practitioner described
in section 1842(b)(18)(C)(i) of the Act (that is, a physician
assistant, nurse practitioner or clinical nurse specialist (as defined
in section 1861(aa)(5) of the Act)). Section 1899(h)(2) of the Act
defines the term ``hospital'' as a hospital (as defined in section
1886(d)(1)(B) of the Act.'' (A ``subsection (d) hospital'' is a
hospital located in one of the fifty States or the District of
Columbia, excluding hospitals and hospital units that are not paid
under the inpatient prospective payment system under section
1886(d)(1)(B) of the Act, such as psychiatric, rehabilitation, long
term care, children's, and cancer hospitals.) Section 1899(h)(3) of the
Act defines the term ``Medicare fee-for-service beneficiary'' as an
individual who is enrolled in the original Medicare FFS program under
Medicare Parts A and B and is not enrolled in a Medicare Advantage (MA)
plan under Medicare Part C, an eligible organization under section 1876
of the Act, or a Program of All-Inclusive Care for the Elderly (PACE)
under section 1894 of the Act.
Section 1899(i) of the Act provides that the Secretary may use
either a partial capitation model or other payment model, rather than
the payment model described in section 1899(d) of the Act, for making
payments under the Shared Savings Program. Sections 1899(i)(2)(B) and
1899(i)(3)(B) of the Act require that any such model maintain budget
neutrality. Specifically, these sections require that any such model
adopted by the Secretary, ``does not result in spending more for such
ACO for such beneficiaries than would otherwise be expended for such
ACO for such beneficiaries for such year if the model were not
implemented, as estimated by the Secretary.''
Finally, section 1899(k) of the Act provides for an extension to
the Physician Group Practice (PGP) demonstration: ``During the period
beginning on the date of the enactment of this section and ending on
the date the program is established, the Secretary may enter into an
agreement with an ACO under the demonstration under section 1866A,
subject to rebasing and other modifications deemed appropriate by the
Secretary.''
C. Overview and Intent of the Medicare Shared Savings Program
The intent of the Shared Savings Program is to promote
accountability for a population of Medicare beneficiaries, improve the
coordination of FFS items and services, encourage investment in
infrastructure and redesigned care processes for high quality and
efficient service delivery, and incent higher value care. As an
incentive to ACOs that successfully meet quality and savings
requirements, the Medicare Program can share a percentage of the
achieved savings with the ACO. In order to meet the intent of the
Shared Savings Program as established by the Affordable Care Act, we
will focus on achieving, as our highest-level goal, the three-part aim,
which consists of the following:
Better care for individuals--as described by all six
dimensions of quality in the Institute of Medicine report: Safety,
effectiveness, patient-centeredness, timeliness, efficiency, and
equity;
Better health for populations with respect to educating
beneficiaries about the upstream causes of ill health--like poor
nutrition, physical inactivity, substance abuse, economic disparities--
as well as the importance of preventive services such as annual
physicals and flu shots; and
Lower growth in expenditures by eliminating waste and
inefficiencies while not withholding any needed care that helps
beneficiaries.
Under the Shared Savings Program, ACOs will only share in savings
if they first generate shareable savings and then meet the quality
standards. In the spirit of the three-part aim and the vision of always
keeping the beneficiary in the forefront of all decisions, we believe
that an ACO should embrace the following goals:
An ACO will put the beneficiary and family at the center
of all its activities. It will honor individual preferences, values,
backgrounds, resources, and skills, and it will thoroughly engage
people in shared decision-making about diagnostic and therapeutic
options.
An ACO will ensure coordination of care for beneficiaries
regardless of its time or place. In an ACO, people will find that they
no longer carry the burden of ensuring that everyone caring for them
has the information they need. Beneficiaries will see that
organizational teamwork improves their health care.
An ACO will attend carefully to care transitions,
especially as beneficiaries journey from one part of the care system to
another.
An ACO will manage resources carefully and respectfully.
It will ensure continual waste reduction, and that every step in care
adds value to the beneficiary. An ACO will be able to make investments
where investments count, and move resources to meet beneficiaries'
needs. Because of its capabilities with respect to prevention and
anticipation, especially for chronically ill people, an ACO will be
able to continually reduce its dependence on inpatient care. Instead,
its patients will more likely be able to be home, where they often want
to be, and, during a hospital admission, they receive assurance that
their discharges will be well coordinated, and that they will not
return due to avoidable complications.
An ACO will be proactive by reaching out to patients with
reminders and advice that can help them stay healthy and let them know
when it is time for a checkup or a test.
An ACO will collect, evaluate, and use data on health care
processes and outcomes sufficiently to measure what it achieves for
beneficiaries and communities over time and use such data to improve
care delivery and patient outcomes.
An ACO will be innovative in the service of the three-part
aim of better care for individuals, better health for populations, and
lower growth in expenditures. It will draw upon the best, most advanced
models of care, using modern technologies, including telehealth and
electronic health records, and other tools to continually reinvent care
in the modern age. It will monitor and compare its performance to other
ACOs, identify and examine new processes for care improvement, and
adopt those approaches that are demonstrated to be effective.
An ACO will continually invest in the development and
pride of its own workforce, including affiliated clinicians. It will
maintain and execute plans for helping build skill, knowledge, and
teamwork.
As proposed in this notice of proposed rulemaking (NPRM), the
Shared Savings Program encourages providers of services and suppliers
to form ACOs that seek to achieve a three-part aim of better care for
individuals, better health for populations, and lower growth in
expenditures. The proposed
[[Page 19534]]
rule establishes the requirements for ACOs to take responsibility for
improving the quality of care they deliver to a group of Medicare FFS
beneficiaries, while lowering the growth in costs, in return for a
share of the resulting savings. In addition to establishing a shared
savings model for rewarding quality and financial performance, the
program also holds ACOs accountable for excess expenditures by
establishing, as an option, a two-sided risk model which requires
repayment of losses to us. This represents a new approach for the
Medicare FFS program, under which providers have traditionally had
little or no financial incentive to coordinate the care for their
patients or to be accountable for the total costs and quality of the
care provided.
Since there is little comparative experience with implementing a
Shared Savings Program and alternative payment models at the national
level, we sought input on the impact of this proposed program from a
wide range of external experts, including credentialed actuaries,
clinical managers, and academic researchers on the potential impact of
the program through, for example, the White House meeting, multiple
listening sessions, Special Open Door Forum on ACOs, Workshop Regarding
ACOs with CMS, OIG, and the Antitrust Agencies, and a Request For
Information. Incorporating their input, we estimate that up to 5
million Medicare beneficiaries will receive care from providers
participating in ACOs, many of which are located in higher cost areas,
and that the program can have a significant impact on lowering Medicare
expenditure growth. Furthermore, projections on the initial impact of
the program by the Congressional Budget Office also suggest the Shared
Savings Program could result in significant savings to the Medicare
program.
We also believe that the Shared Savings Program should provide an
entry point for all willing organizations who wish to move in a
direction of providing value-driven healthcare. Consequently, in
accordance with the authority granted to the Secretary under section
1899(i) of the Act, we are proposing for comment creating and
implementing both a shared savings model (one-sided model) and a shared
savings/losses model (two-sided model). Under this proposal, balanced
maximum sharing rates under the two options to provide greater reward
for ACOs accepting risk while maintaining an incentive to encourage
ACOs not immediately ready to accept risk to participate in the one-
sided model. This approach provides an entry point for organizations
with less experience managing care and accepting financial risk, such
as physician-driven organizations or smaller ACOs, to gain experience
with population management in the FFS setting before transitioning to
more risk.
We believe that ACOs electing to initially enter the one-sided
model automatically transition to a two-sided risk model during the
final year of their initial agreement. We also believe that a two-sided
model that builds off a one-sided model could be offered as an option
at the beginning of the program. We would immediately reward ACOs
electing to enter the two-sided model with higher sharing rates
available under that model. This approach provides an opportunity for
more experienced ACOs that are ready to accept risk to enter a sharing
arrangement that provides greater reward for greater responsibility.
For more detail on the two-sided risk model refer to section II.G. of
this proposed rule.
In addition to the opportunity to implement alternative payment
models such as partial capitation under 1899(i) of the Act, the Center
for Medicare and Medicaid Innovation (Innovation Center), created by
the Affordable Care Act also has authority to test innovative payment
models. As we gain experience with the shared savings model and
alternative payment models, we will continue to refine and improve the
program over time to make it increasingly effective in achieving our
three-part aim of better care for individuals, better health for
populations, and lower growth in expenditures. Finally, in developing
the Shared Savings Program, and in response to stakeholder suggestions,
we have worked very closely with agencies across the Federal government
to develop policies to encourage participation and to ensure a
coordinated and aligned inter- and intra-agency effort in the
implementation of the program. The result of this effort is the release
of several notices with which potential participants are strongly
encouraged to become familiar. Detailed descriptions of these notices
appear in section II.I of this proposed rule, and include: (1) A joint
CMS and DHHS OIG Medicare Program; Waiver Designs in Connection with
the Medicare Shared Savings Program and the Innovation Center; (2) an
Internal Revenue Service (IRS) notice soliciting comments regarding the
need for additional tax guidance for tax-exempt organizations,
including tax-exempt hospitals, participating in the Shared Savings
Program; and (3) a proposed Antitrust Policy Statement issued by the
FTC and DOJ (collectively, the Antitrust Agencies).
D. Related Affordable Care Act Provisions
The Affordable Care Act intends to improve quality and make health
care more affordable through the Shared Savings Program as well as
through other provisions. There are four programs authorized by the
Affordable Care Act discussed later in the document which may affect
Shared Savings Program policy or help to guide future Shared Savings
Program policy, or may intersect with the Shared Savings Program in
other ways.
1. Establishment of Center for Medicare and Medicaid Innovation
(Innovation Center)
Section 1115A of the Act, as added by section 3021 of the
Affordable Care Act, required the establishment of the new Innovation
Center not later than January 1, 2011 to test innovative payment and
service delivery models to reduce program expenditures under Medicare,
Medicaid, and the Children's Health Insurance Program (CHIP) while
preserving or enhancing the quality of care furnished to beneficiaries
under these programs. In selecting such models for testing, the statute
requires the Secretary to give preference to models that also improve
the coordination, quality, and efficiency of health care services
furnished under Medicare, Medicaid, and CHIP.
Section 1115A authorizes the Secretary to expand the duration and
scope of a model being tested through rulemaking (including
implementation on a nationwide basis) to the extent the Secretary--
Determines expected expansion to reduce spending under the
applicable title without reducing the quality of care or improve the
quality of patient care without increasing spending;
Obtains a certification from our Chief Actuary that such
expansion would reduce (or would not result in any increase in) net
program spending under applicable titles; and
Determines that such expansion would not deny or limit the
coverage or provision of benefits under Medicare, Medicaid, or CHIP.
Through the Innovation Center, we plan to explore alternative
payment models for the Shared Savings Program. As we test and refine
these models, gain operational experience, and put the necessary
infrastructure in place to support program wide implementation,
including critical monitoring and
[[Page 19535]]
patient protection infrastructure, we plan to make these options
available under the Shared Savings Program in future rulemaking. Our
intent is to move participants of the demonstration models that have a
demonstrated track record of realizing shared savings and high quality
performance into the Shared Savings Program in future agreement
periods.
2. Independence at Home Medical Practices
Section 1866E of the Act, as added by section 3024 of the
Affordable Care Act authorizes the Secretary to conduct a demonstration
program to test a payment incentive and service delivery model that
utilizes Independence at Home Medical Practices, which are comprised of
physician and nurse practitioner directed home-based primary care
teams, to provide services designed to reduce expenditures and improve
health outcomes for certain Medicare beneficiaries.
Subject to performance on quality measures established for the
demonstration, participating practices may be eligible to receive an
incentive payment in the form of shared savings. In determining whether
savings were generated, the Secretary shall establish an estimated
annual spending target, for the amount the Secretary estimates would
have been spent in absence of the demonstration, for items and services
covered under Parts A and B furnished to applicable beneficiaries for
each qualifying Independence at Home medical practice. A practice is
eligible to receive an incentive payment if actual expenditures for the
year for the applicable beneficiaries it enrolls are less than the
estimated spending target established for the year. An incentive
payment for each year shall be equal to a portion of the amount by
which actual expenditures for applicable beneficiaries under Parts A
and B for the year are estimated to be less than 5 percent less than
the estimated spending target for the year.
3. State Option To Provide Health Homes
Section 1945 of the Act, as added by section 2703 of the Affordable
Care Act authorizes a State option under Medicaid to provide a health
home for individuals with chronic conditions. The definition of the
term ``health home'' is defined as a designated provider (including a
provider that operates in coordination with a team of health care
professionals) or a health team selected by an eligible individual with
chronic conditions to provide health home services. Health home
services are defined as comprehensive and timely high-quality services,
including comprehensive care management; care coordination and health
promotion; comprehensive transitional care, including appropriate
follow-up, from inpatient to other settings; patient and family support
(including authorized representatives); referral to community and
social support services, if relevant; and use of health information
technology to link services, as feasible and appropriate.
Under section 1945 of the Act, States pay the designated provider,
team of health care professionals operating with such a provider, or
health team for the provision of health home services to each eligible
individual with chronic conditions that selects them as their health
home. A State specifies in their State plan amendment the methodology
it will use to determine payment for health home services. The
methodology may be tiered to reflect, with respect to each eligible
individual with chronic conditions, the severity or number of such
individual's chronic conditions or the specific capabilities of the
provider, team of health care professionals, or health team. A time-
limited higher Federal Medicaid matching payment is available for
health home services.
4. Community Health Teams
Section 3502 of the Affordable Care Act requires the Secretary to
establish a program to provide grants to or enter into contracts with
eligible entities to establish community based interdisciplinary,
inter-professional teams (referred to in the statute as ``health
teams'') to support primary care practices, including obstetrics and
gynecology practices, within the hospital service areas served by the
eligible entities. These grants or contracts shall be used to establish
health teams to provide support services to primary care providers and
provide capitated payments to primary care providers as determined by
the Secretary. For purposes of this section, primary care is the
provision of integrated, accessible health care services by clinicians
who are accountable for addressing a large majority of personal health
care needs, developing a sustained partnership with patients, and
practicing in the context of the family and community.
A health team established under a grant or contract must establish
contractual agreements with primary care providers to provide support
services. The team must support patient-centered medical homes, defined
as a mode of care that includes--(1) Personal physicians; (2) whole
person orientation; (3) coordinated and integrated care; (4) safe and
high-quality care through evidence-informed medicine, appropriate use
of health information technology, and continuous quality improvements;
(5) expanded access to care; and (6) payment that recognizes added
value from additional components of patient centered care.
Health teams must also collaborate with local primary care
providers and existing State and community-based resources to
coordinate--(1) disease prevention; (2) chronic disease management; (3)
transitioning between health care providers and settings; and (4) case
management for patients, including children, with priority given to
those amenable to prevention and with chronic diseases or conditions
identified by the Secretary. In collaboration with local health care
providers, a health team must develop and implement interdisciplinary,
interprofessional care plans that integrate clinical and community
preventive and health promotion services for patients, including
children, with a priority given to those amenable to prevention and
with chronic diseases or conditions identified by the Secretary.
E. Related Ongoing CMS Efforts
1. Physician Group Practice Demonstration
We have previous experience developing and implementing shared
savings models through demonstrations. First, under section 412 of the
Medicare, Medicaid, and CHIP Benefits Improvement and Protection Act of
2000 (BIPA), we implemented the Physician Group Practice (PGP)
Demonstration in April of 2005--our first attempt at establishing a
Shared Savings ACO model. The PGP Demonstration offered a unique
payment model by which PGP providers received their normal Parts A and
B FFS payments for services rendered and offered an additional
performance payment for demonstrating ``value.'' The performance
payments were tied directly to achieving targets for process and
outcome quality measures as well as cost savings. The PGP Demonstration
showed that physician-driven organizations are willing to engage in
efforts to improve the overall quality and cost efficiency of care for
the patient population they serve. Under the demonstration, the PGPs
were accountable for a patient population to whom they provided the
plurality of office-based evaluation and
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management care. The assignment of patients to the PGP at the end of
each performance year and data has shown that assigned patients had on
average four or five visits at the PGP during the year. This provided
the opportunity for the organizations to better coordinate services and
improve the quality and efficiency of care provided to Medicare FFS
patients. Medicare patients retained their entitlement to see any
Medicare provider they chose and were not enrolled or required to only
see PGP physicians under the demonstration.
Based on their experience with the PGP demonstration, participants
identified several factors as critical to improving quality and the
opportunity to share savings:
An integrated organization with an environment that
supports expending resources on multiple programs and initiatives to
improve quality and reduce unnecessary services.
Dedicated physician leadership with a proven ability to
motivate physicians to participate in the development and
implementation of quality improvement and other clinical programs and
initiatives.
Health information technology that facilitates the
aggregation and analysis of data, allows patient-level feedback, and
provides alerts and reminders at the point of care.
Experience with non-Medicare payer initiatives,
particularly through a managed care affiliate, to improve quality and
reduce expenditure growth.
Under the demonstration, at the end of the third performance year,
all 10 of the PGPs continued to improve the quality of care for
patients with chronic illness or who required preventive care by
achieving benchmark or target performance on at least 28 out of 32
quality markers for patients with diabetes, coronary artery disease,
congestive heart failure, hypertension, and for cancer screening. Two
of the PGPs achieved benchmark quality performance on all 32 quality
measures. Over the course of the first three years, 6 of the 10 groups
shared in approximately $46 million in savings.
2. Medicare Health Care Quality Demonstration
We have begun testing models under the Medicare Health Care Quality
(MHCQ) Demonstration, created by the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA) (Pub. L. 108-173).
Section 1866C(b) of the Act, as added by section 646 of the MMA,
required the Secretary to establish a 5-year demonstration program
under which the Secretary was required to approve demonstration
projects that examine health delivery factors that encourage the
delivery of improved quality in patient care. Section 3021(c) of the
Affordable Care Act amended section 1866C of the Act to allow the
Secretary to expand, through rulemaking, the duration and scope of a
demonstration the Secretary is conducting under that section to the
extent determined appropriate by the Secretary if the demonstration
meets certain criteria. The MHCQ Demonstration Projects design examine
the extent to which major, multi-faceted changes to traditional
Medicare's health delivery and financing systems lead to improvements
in the quality of care provided to Medicare beneficiaries, without
increasing total program expenditures. We approved one such program,
the Indiana Health Information Exchange (IHIE).
Beginning July 1, 2009, we began the first MHQC project, the IHIE's
implementation of a regional, multi-payer, pay-for-performance and
quality reporting program, based (by-and-large) on a common set of
quality measures. The expectation is such that the IHIE's interventions
provide important empirical evidence on the effectiveness of pay-for-
performance, health IT, and multipayer initiatives in improving the
quality and efficiency of care provided to Medicare beneficiaries.
IHIE aggregates our claims and administrative data in the
demonstration with other data processed in conjunction with its
regional health information exchange (HIE). Data used from the various
sources generate patient-level and provider level quality reports,
alerts, and reminders for participating providers. By incorporating our
data into IHIE's HIE and producing these quality reports, IHIE can
provide participating physicians with a more complete picture of the
care that is or is not being provided to their Medicare patients and
give physicians the information they need to positively impact the
quality and cost of care being provided.
During the demonstration, we review cost and quality data for
Medicare FFS beneficiaries that have at least one office or other
outpatient evaluation and management (E&M) visit with an IHIE
participating physician. It is expected that an estimated 100,000
Medicare beneficiaries residing in the Indianapolis metropolitan area
will meet this criterion in each year of the demonstration.
Quality of care is measured at the population-level (that is,
performance measurement will focus on whether or not the site has
achieved improvements in quality when looking at the entire group of
treated patients) using a set of Medicare specific quality measures.
Improvements in the quality of care provided to Medicare beneficiaries
are determined on the extent to which IHIE participating physicians are
able to reduce the gap between the maximum attainable level for a
quality measure and the baseline performance for the quality measure.
We used approximately 14 ambulatory care quality measures in the first
year, growing to approximately 30 in the fifth year.
Quality-contingent shared savings are available with our
calculating savings in the intervention population by comparing actual
costs to expected costs for treated beneficiaries. Expected costs for
the in