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Medicare Program Changes in the Senate
Amendment in the Nature of a Substitute to
H.R. 3590

Patricia A. Davis, Coordinator
Specialist in Health Care Financing
Jim Hahn
Analyst in Health Care Financing
Paulette C. Morgan
Specialist in Health Care Financing
Holly Stockdale
Analyst in Health Care Financing
Julie Stone
Specialist in Health Care Financing
Sibyl Tilson
Specialist in Health Care Financing
December 4, 2009
Congressional Research Service
7-5700
www.crs.gov
R40970
CRS Report for Congress
P
repared for Members and Committees of Congress

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Medicare Program Changes in the Senate Amendment

Summary
Medicare is a federal program that pays for covered health services for most persons 65 years and
older and for most permanently disabled individuals under the age of 65 years. The rising cost of
health care, the impact of the aging baby boomer generation, and declining revenues in a
weakened economy continue to challenge the program’s ability to provide quality and effective
health services to its 45 million beneficiaries in a financially sustainable manner.
On November 18, 2009, Senate Majority Leader Harry Reid unveiled the Senate Amendment in
the nature of a substitute to H.R. 3590, the Patient Protection and Affordable Care Act. This
report, one of a series of CRS products on this Senate Amendment, examines the Medicare
related provisions in this Amendment. Estimates from CBO on the Senate Amendment indicate
that net reductions in Medicare direct spending may approach $400 billion from FY2010 to 2019.
Major savings are expected from constraining Medicare’s annual payment increases for certain
providers, basing payment rates in the Medicare Advantage program on average bids, reducing
payments to hospitals that serve a large number of low-income patients, creating an independent
Medicare Advisory Board to make changes in Medicare payment rates, and modifying the high-
income threshold adjustment for Part B premiums. A new Hospital Insurance tax for high wage
earners would also raise approximately $54 billion over 10 years.
Other provisions in the Amendment address more systemic issues such as increasing the
efficiency and quality of Medicare services, and strengthening program integrity. For example,
the Amendment would establish a national, voluntary pilot program that would bundle payments
for physician, hospital and post-acute care services with the goal of improving patient care and
reducing spending. Another provision would adjust payments to hospitals for readmissions related
to certain potentially preventable conditions. Additionally, the Amendment would increase
funding for anti-fraud activities, and subject providers and suppliers to enhanced screening before
allowing them to participate in the Medicare program.
The Senate Amendment would also improve some benefits provided to Medicare beneficiaries.
For instance, Medicare prescription drug program enrollees would receive a 50% discount off the
price of brand name drugs during the coverage gap (the “doughnut hole”) and the coverage gap
would be reduced by $500 in 2010. Other provisions would expand assistance for some low-
income beneficiaries enrolled in the Medicare drug program, and eliminate beneficiary
copayments for certain preventive care services.

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Medicare Program Changes in the Senate Amendment

Contents
Introduction ................................................................................................................................ 1
Congressional Budget Office (CBO) Score.................................................................................. 1
Payment Rate Changes Affecting Medicare Fee-for-Service Providers......................................... 3
Hospitals and Other Part A Providers..................................................................................... 4
Acute Care Hospitals ...................................................................................................... 4
Skilled Nursing Facilities (SNFs) .................................................................................... 5
Home Health Agencies (HHAs) ...................................................................................... 6
Physicians and Other Part B Providers .................................................................................. 7
Payment and Administrative Changes Affecting the Medicare Advantage Program...................... 8
Changes Affecting Medicare’s Prescription Drug Benefit ............................................................ 9
Efforts to Improve the Efficiency and Quality of Health Care Services Provided Under
Medicare................................................................................................................................ 10
Changes to Address Medicare Sustainability ............................................................................. 11
Changes to Address Fraud, Waste, and Abuse ............................................................................ 12
Concluding Observations .......................................................................................................... 13

Appendixes
Appendix. Selected Medicare Provisions in the Senate Amendment (S.Amdt. 2786) in the
Nature of a Substitute to H.R. 3590 ........................................................................................ 15

Contacts
Author Contact Information ...................................................................................................... 69
Acknowledgments .................................................................................................................... 69

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Medicare Program Changes in the Senate Amendment

Introduction
On November 18, 2009, the proposed Senate Amendment in the Nature of a Substitute to H.R.
3590 (“the Amendment”), was made public.1 If adopted, the Amendment would replace the
substantive text of H.R. 3590 with the text of the Patient Protection and Affordable Care Act. The
Amendment contains numerous provisions affecting Medicare payments, payment rules, covered
benefits, and the delivery of care. On December 3, 2009, S.Amdt. 2826, which would add an
additional provision to (“the Amendment”) related to protecting and improving Medicare
benefits, was agreed to in the Senate.
The Congressional Budget Office (CBO) estimates that, under current law, total mandatory
annual expenditures for Medicare will grow from $498 billion in 2009 to $942 billion in 2019.2
Cumulative spending for the years 2010 to 2019 is expected to exceed $7 trillion. CBO estimates
on the Senate Amendment provisions affecting Medicare indicate that, absent interaction effects,
net reductions in Medicare direct spending may approach $400 billion over the FY2010-2019
period.
The proposed legislation includes nine titles. This report discusses selected provisions in Titles II,
III, IV, V, VI and IX in the Amendment concerning payment and program modifications to
Medicare’s fee-for-service program, its prescription drug benefit, and the Medicare Advantage
(MA) program; efforts to reform Medicare’s payment methods, program integrity changes to
address fraud, waste and abuse, and other miscellaneous Medicare changes. Provisions that would
modify Medicare’s graduate medical education payments to teaching hospitals, some quality
measurement efforts, and other public health initiatives are not covered.3 The body of this report
includes a discussion of the financial impact on the Medicare program by the Amendment
established by the CBO (the CBO score), then provides an overview of Medicare changes by
provider type and program, followed by a brief discussion of the changes to address efficiencies
and quality in Medicare, efforts to address long-term Medicare financing, and program integrity
changes.4 The Appendix, Selected Medicare Provisions in the Senate Amendment (S.Amdt.
2786) in the Nature of a Substitute to H.R. 3590, provides a brief current law description,
explanation of the proposed change and the CBO score for most of the Medicare provisions in the
Senate Amendment.
Congressional Budget Office (CBO) Score
On November 18, 2009, the CBO and the staff of the Joint Committee on Taxation completed
their analyses of the Senate Amendment in the Nature of a Substitute to H.R. 3590, the Patient
Protection and Affordable Care Act. Their analyses provide estimates of the direct spending and

1 The Amendment in the nature of a substitute to H.R. 3590 (S.Amdt. 2786) may be found at
http://democrats.senate.gov/reform/patient-protection-affordable-care-act.pdf.
2 CBO’s Baseline Projections of Mandatory Spending, August 2009, Table 1-4. http://www.cbo.gov/ftpdocs/105xx/
doc10521/budgetprojections.pdf.
3 Those provisions are discussed in CRS Report R40943, Public Health, Workforce, Quality, and Related Provisions in
the Senate Amendment in the Nature of a Substitute to H.R. 3590
, coordinated by C. Stephen Redhead and Erin D.
Williams.
4 Background information on the Medicare program can be found in the CRS Report R40425, Medicare Primer.
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revenue effects of the Amendment.5 The estimates do not, however, include certain administrative
costs that would be incurred by the government to implement the changes.
CBO estimates that the provisions in the Amendment that would affect the Medicare, Medicaid,
Children’s Health Insurance and other federal programs would reduce direct spending by $491
billion over the FY2010-FY2019 period.6 Medicare (absent interaction affects) accounts for
almost $400 billion of the reduction. Total Medicare reductions in direct spending over the 10-
year period are estimated to be about $450 billion, but these reductions would be offset by
Medicare payment increases of close to $50 billion. As noted by CBO, the provisions that would
result in the largest savings include:
• Permanent reductions in the annual updates to Medicare’s fee-for-service
payment rates (other than physicians’ services) would account for an estimated
budgetary savings of $192 billion over 10 years;7
• Setting payment rates in the Medicare Advantage program on the basis of the
average bids submitted by MA plans in each market would account for an
estimated $118 billion in savings (before interactions) over 10 years;
• Reducing Medicare payments to hospitals that serve a large number of low-
income patients, known as disproportionate share (DSH) hospitals, would
decrease expenditures by about $21 billion;
• Modifying the high-income adjustment for Part B premiums would save
$24 billion over 10 years; and
• Creating an Independent Medicare Advisory Board to make changes in Medicare
payment rates is expected to save $23 billion over 10 years.
Additionally, a new Hospital Insurance tax on taxable wages over $200,000 per year for single
filers ($250,000 for joint filers) is expected to raise $54 billion from FY2013 through FY2019.
CBO estimates that Medicare spending under the bill would increase more slowly over the next
20 years compared to the past 20 years—a 6% average annual rate compared to the prior 8%.
CBO notes, however, that their estimates are subject to uncertainty. For example, this savings rate
assumes that the sustainable growth rate (SGR) mechanism that constrains Medicare physician
payment rates would go back into effect in 2011 (a year after the one-time increase in 2010
provided for under the Amendment), at which time physicians would be facing an approximate
23% cut in payments. The longer term projections also assume that the Independent Medicare
Advisory Board established by this Amendment would be effective in reducing costs. CBO could
not determine whether the reduction in the growth rate would be achieved through greater
efficiencies in the delivery of health care or if the payment reductions would lead to lower quality
of care.

5 The CBO score can be found at http://www.cbo.gov/ftpdocs/107xx/doc10731/Reid_letter_11_18_09.pdf. The JCT
score may be found at http://www.jct.gov/publications.html?func=startdown&id=3635.
6 The estimated overall effect of the proposed legislation is a net decrease in the federal budget deficit of $130 billion
over the FY2010-FY2019 period. The projected 10-year cost of increasing insurance coverage of $599 billion is offset
by the net spending decrease of $491 billion and by revenue provisions that are estimated to raise $238 billion over the
same period.
7 This estimate excludes interaction effects including the impact on these reductions to payments to Medicare
Advantage plans and on the collection of Part B premiums.
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Payment Rate Changes Affecting Medicare Fee-for-
Service Providers

Medicare is a federal program that pays for covered health services for most persons 65 years of
age and older and for most permanently disabled individuals under the age of 65. It consists of
four parts, each responsible for paying for different benefits, subject to different eligibility criteria
and financing mechanisms.8 Under traditional Medicare, Part A and Part B services are typically
paid on a fee-for-service basis (each service or group of services provided to a patient is
reimbursed through a separate payment) using different prospective payment systems (PPS) or
fee schedules.9 Certain other services are paid on the basis of reasonable costs or reasonable
charges.
In general, each year, the Centers for Medicare and Medicaid Services (CMS) issues regulations
to set Medicare’s payment rates to specific providers, physicians, practitioners and suppliers for
the upcoming year. For instance, the program provides for annual updates of Medicare payments
to reflect inflation and other factors. In some cases, these updates are linked to the consumer price
index for all urban consumers (CPI-U) or to a provider-specific market basket (MB) index which
measures the change in the price of goods and services purchased by the provider to produce a
unit of output. While CMS implements the payment methods through detailed rule-making,
typically, the basic parameters for setting these payments, including updates over time, have been
established by Congress.
In March of each year, the Medicare Payment Advisory Commission (MedPAC) makes payment
update recommendations concerning Medicare’s different fee-for-service payment systems to
Congress.10 To do so, MedPAC staff first examines the adequacy of the Medicare payments for
efficient providers in the current year and then assesses how provider costs are likely to change in
the upcoming year, including scheduled policy changes that will affect Medicare’s payment
rates.11 As stated by MedPAC, Medicare’s payment systems should encourage efficiency and
Medicare providers can achieve efficiency gains similar to the economy at large. This policy
target links Medicare’s expectations for efficiency improvements to the productivity gains
achieved by firms and workers who pay taxes that fund Medicare. The amount, if any, of
MedPAC’s update recommendations will depend on its overall assessment of the circumstances
of a given set of providers in any year. To differing extents, MedPAC’s analyses and

8 Part A, the Hospital Insurance program, covers hospital services, up to 100 days of post-hospital skilled nursing
facility services, post-institutional home health visits, and hospice services. Part B, the Supplementary Medical
Insurance program, covers a broad range of medical services including physician services, laboratory services, durable
medical equipment, and outpatient hospital services. Part B also covers some home health visits. Part C provides
private plan options, such as managed care, for beneficiaries who are enrolled in both Parts A and B. Part D provides
optional outpatient prescription drug coverage.
9 Medicare has specific rules for fee-for-service payments under Parts A and B as well as capitation (or per person)
payments under Part C. Outpatient prescription drugs covered under Part D are not subject to Medicare payment rules.
Prices are determined through negotiation between prescription drug plans (PDPs), or Medicare Advantage Prescription
Drug (MA-PD) plans, and drug manufacturers. The Secretary of Health and Human Services is statutorily prohibited
from intervening in Part D drug price negotiations.
10 Medicare Payment Advisory Commission (MedPAC) Report to Congress: Medicare Payment Policy, March 2009,
http://www.medpac.gov/documents/Mar09_EntireReport.pdf.
11 See pp. 35-41 of Medicare Payment Advisory Commission (MedPAC) Report to Congress: Medicare Payment
Policy
, March 2009 for a discussion of their update framework.
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recommendations have shaped provisions in the Senate Amendment; that influence is noted in
this report wherever applicable.
Hospitals and Other Part A Providers
Part A provides coverage for inpatient hospital services, post-hospital skilled nursing facility
(SNF) services, post-hospital home health services, and hospice care, subject to certain conditions
and limitations. Approximately 20% of beneficiaries enrolled in Part A use these services during
any year. CBO estimates that about $223 billion was spent on Part A benefits in 2008, an amount
that is projected to increase to $435.2 billion in 2019. In part because of its sheer size, provisions
reducing Part A spending comprise a significant proportion of the savings attributed to this
legislation either through constraining payment updates or by other payment changes.
Acute Care Hospitals
Generally, the provisions of the Senate Amendment affecting Medicare’s payments to acute care
hospitals would constrain payment increases to these hospitals, restructure payments to address
treatment inefficiencies, and then reshape Medicare’s disproportionate share hospital (DSH)
hospital subsidies. Also, the exception which permits physicians with ownership interests in a
hospital to refer Medicare and Medicaid patients to that hospital would be eliminated for new
physician-owed hospitals or those that did not meet certain criteria.
Specifically, the amendment would adjust Medicare’s annual payment updates to Part A hospitals
to account for economy-wide productivity increases for cost savings (along with certain other
reductions) which is estimated to reduce Medicare spending significantly over 10 years. Under
current law, the market basket component of the physician update or the Medicare economic
index (MEI) is adjusted to exclude productivity gains. This provision uses the same measure of
productivity improvement, the 10-year moving average of all-factory productivity, which is
included in the MEI. This estimated savings include the reduction for outpatient and inpatient
services for all hospitals; the savings from extending this policy to only acute care hospitals were
not separately identified.
Since 1986, an increasing number of acute care hospitals have received additional payments
under Medicare’s inpatient prospective payment system (IPPS) because they serve a
disproportionate share of low-income patients. The justification for this subsidy has changed over
time. Originally, the DSH adjustment was intended to compensate hospitals for their higher
Medicare costs associated with the provision of services to a large proportion of low-income
patients. Now, the adjustment is considered as a way to protect access to care for Medicare
beneficiaries. The Amendment would reduce hospitals’ DSH payments starting in FY2015 equal
to 25% of what otherwise be made, a payment that represents the empirically justified amount as
determined by MedPAC in its March 2007 Report to Congress. Acute care hospitals would be
paid additional amounts which would depend on the difference in the hospital’s DSH payments
under this legislation; the difference in the percentage change in the uninsured under-65
population from 2012; and the percentage of uncompensated care provided by the hospital
(relative to all acute care hospitals). CBO has estimated that this policy would save $20.6 billion
from FY2015 to FY2019.
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Skilled Nursing Facilities (SNFs)
Medicare covers nursing home services for beneficiaries who require skilled nursing care and/or
rehabilitation services following a hospitalization of at least three consecutive days. The Balanced
Budget Act of 1997 (BBA 97, P.L. 105-33) required the Secretary to establish a prospective
payment system (PPS) for SNF care to be phased in over three years, beginning in 1998. Under
the PPS, SNFs receive a daily payment that covers all the services provided that day, including
room and board, nursing, therapy, and drugs, as well as an estimate of capital-related costs. Any
profits are retained by the SNF, and any losses must be absorbed by the SNF. The daily base
payment is based on 1995 costs that have been increased for inflation and vary by urban or rural
location. A portion of these daily payments is further adjusted for variations in area wages, using
the hospital wage index, to account for geographic variation in wages. SNF per diem PPS
payments are also adjusted to include a temporary 128% increase for any SNF residents who are
HIV-positive or have Acquired Immune Deficiency Syndrome. Section 1888(e) of the Social
Security Act requires that the base payments be adjusted each year by the SNF MB update—that
is, the measure of inflation of goods and services used by SNFs.
In the final FY2010 rule, CMS describes its proposal to recalibrate the case mix indexes to better
account for the resources used in the care of the medically complex and to improve upon its
payment refinements made in 2006.12 According to CMS, the total impact of these changes for
FY2010, accounting for a MB increase of 2.2 percentage points, would be a decrease in Medicare
payments for FY2010 to SNFs of 1.1% (or $360 million) below FY2009 payments. Some
individual providers could experience larger decreases in payments than others due to case-mix
utilization. The proposed PPS and Consolidated Billing SNF payment regulation for FY2010
describes how the Secretary would recalibrate the case-mix indexes (CMIs) for 2010 to more
accurately match the service needs of beneficiaries.
Although MedPAC finds that Medicare payments to SNFs overall are adequate, it has raised
concerns about the efficiency of the payment categories pertaining to nontherapy ancillary (NTA)
services (e.g., prescription drugs, medical equipment and supplies, IV therapy) and therapy
services. To better account for SNF stays with exceptionally high ancillary care needs, MedPAC
recommends, in a June 2009 letter to the Secretary13 and its March 2009 Report,14 that the
Secretary revise the PPS by separating payments for NTA from the bundled PPS rate and by
establishing an outlier policy for stays with exceptionally high NTA costs. In addition, MedPAC
explains that the current reimbursement system for therapy costs encourages the under provision
of therapy services to patients. To improve payments for therapy, MedPAC recommends that the
Secretary recalibrate the payment category for therapy costs so as to better match such payments
to the actual amount of therapy services needed by patients. MedPAC also recommends that the
market basket update for 2010 be eliminated.
On another note, as Medicare beneficiaries with complex health conditions and multiple co-
morbidities can experience multiple hospital readmissions, moving between hospital stays and a

12 Centers for Medicare and Medicaid Services, “Medicare Program; Prospective Payment System and Consolidated
Billing for Skilled Nursing Facilities for FY 2010; Minimum Data Set, Version 3.0 for Skilled Nursing Facilities and
Medicaid Nursing Facilities,” 74 Federal Register 153, August 11, 2009.
13 Letter from Glenn M. Hackbarth, J.D., Chairman, Medicare Payment Advisory Commission, to Charlene Frizerra,
Acting Administrator, Centers for Medicare and Medicaid Services, June 29, 2009.
14 MedPAC’s March 2009 Report, Section 2D, pp. 157-182.
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range of post-acute care providers, including SNFs, In addition, some policy makers, analysts,
and health care practitioners consider relatively high readmission rates for persons with chronic
illnesses to be a symptom of a payment system under Medicare that works less well for the
management of chronically ill patients who leave the hospital and enter other care settings.
MedPAC, among others, has suggested that Medicare test new incentives and payment models to
encourage providers to better coordinate across patients’ episodes of care and to evaluate the full
spectrum of care a patient may receive during these episodes within a hospital, during a patient’s
discharge, and post-hospitalization.
The provisions contained in the Senate Amendment would make all SNF market-basket annual
updates subject to a productivity adjustment starting in FY2012. Under the Amendment, the rate
of growth in payments to SNFs would likely slow and could fall below zero. In addition, certain
Medicare-certified SNFs, together with certain hospitals, physicians and other post-acute care
providers, would be part of National Pilot Program on Payment Bundling. Such a pilot would test
the effectiveness of bundled payments to provide incentives for multiple providers coordinate a
patient’s care around a hospitalization. The Secretary would also be required to develop a plan,
and submit it to Congress no later than October 1, 2011, to implement a Medicare value-based
purchasing program for SNFs, among others.
Home Health Agencies (HHAs)
Home health agencies (HHAs) are paid under a prospective payment system (PPS), which covers
skilled nursing, therapy, medical social services, aide visits, medical supplies, and other services.
Durable medical equipment is not included in the home health PPS. The base payment amount for
the national standardized 60-day episode rate is increased annually by an update factor that is
determined, in part, by the projected increase in the home health market basket (MB) index. This
index measures the changes in the costs of goods and services purchased by HHAs. HHAs are
currently required to submit to the Secretary health care quality data. An HHA that does not
submit the required quality data will receive an update of the MB minus two percentage points for
that fiscal year.
The proposed rule for calendar year (CY) 2010 reports that the HH MB will increase by 2.2% for
that year.15 In addition, in an effort to address potential fraud and abuse in the use of HH outlier
payments, CMS proposes to cap outlier payments at 10% of total HH PPS payments and to target
outlier payments to be no greater than 2.5% of total HH PPS payments, among other things.
In CY2008, CMS made refinements to the home health (HH) PPS to try to improve payment
efficiencies. Specifically, this regulation established changes to the home health agency (HHA)
case-mix index to account for the relative resource utilization of different patients. These changes
modified the coding or classification of different units of service that do not reflect real changes
in case-mix. As a result, the national prospective 60-day episode payment rate was adjusted
downward by 2.75% for CY2008, by 2.75% for each year of CY2009 and CY2010, and by 2.71%
for CY2011.
In its March 2009 Report, MedPAC explains that payments to HHAs have exceeded costs by a
wide margin since the PPS was implemented in 2000. As a result, MedPAC recommends that the

15 Centers for Medicare and Medicaid Services, “Medicare Program; Home Health Prospective Payment System; Rate
Update for Calendar Year 2010,” 74 Federal Register 216, November 10, 2009.
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MB increase for 2010 be eliminated and that the payment coding changes scheduled by the
Secretary be accelerated. Further, MedPAC recommends that HHA rates be rebased to better
reflect the average costs of care.
Two provisions in the Senate Amendment would impact HH payments. The first would reduce the
HH MB update by 1.0 percentage point in 2011 and 2012, and all HH MB annual updates would
be subject to a productivity adjustment starting in 2015. Under the Amendment, the rate of
growth in payments to HHAs would likely slow and could fall below zero. The second would
require the Secretary, starting in CY2013, to rebase home health payments by a percentage
considered appropriate by the Secretary to, among other things, reflect the number, mix and level
of intensity of HH services in an episode, and the average cost of providing care. Starting in
CY2011, the Secretary would be directed to establish a provider-specific annual cap of ten
percent of revenues that a HH agency may be reimbursed in a given year from outlier payments.
For visits ending on or after April 1, 2010 and before January 1, 2016, the Secretary would be
directed to provide for a three percent add-on payment for HH providers serving rural areas.
The Secretary would also be required to develop a plan, and submit it to Congress no later than
October 1, 2011, to implement a Medicare value-based purchasing program for HHAs, among
others. In addition, certain Medicare-certified SNFs, together with certain hospitals, physicians
and other post-acute care providers, would be part of National Pilot Program on Payment
Bundling. Such a pilot would test the effectiveness of bundled payments to provide incentives for
multiple providers to coordinate a patient’s care around a hospitalization.
Physicians and Other Part B Providers
The Senate Amendment would make several changes to how Medicare payments to physicians
are determined and to physician reporting and feedback programs. These modifications include
refinements to the calculation of the payments, the introduction of new bonus payments, and
adjustments to existing programs for physicians. The payment reduction as determined under the
sustainable growth rate (SGR) system would be averted by a one-year 0.5% increase for
physician payments in 2010.16
In addition, the Amendment would give the Secretary (through CMS) additional flexibility to be
able to review and adjust potentially misvalued codes under the physician fee schedule, extend
the floor for the index representing geographic variation in physician work used in determining
payments, extend the payment for the technical component of certain pathology services, and
modify the payment for imaging services to more closely reflect the actual use of the equipment.
The Senate Amendment would also modify the physician quality reporting initiative program
(PQRI) and extend the years of the bonus payments while introducing a penalty for non-reporting
in future years.

16 For more detail on the SGR system and Medicare physician payments, see CRS Report R40907, Medicare Physician
Payment Updates and the Sustainable Growth Rate (SGR) System
, by Jim Hahn.
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Payment and Administrative Changes Affecting the
Medicare Advantage Program

The Senate Amendment would change how the maximum possible payment to Medicare
Advantage (MA) plans is determined, in addition to other payment and administrative changes.
Payments to MA plans are determined by comparing a plan’s cost of providing required Medicare
benefits (bid) to the maximum amount Medicare will pay for those benefits in each area
(benchmark). Historically, Congress has increased the benchmark amounts through statutorily
specified formulas, in part, to encourage plan participation in all areas of the country. As a result,
the benchmark amounts in some areas are higher than the average cost of original fee-for-service
Medicare. The Amendment would require the benchmark to be determined based on the weighted
average of MA plan bids, rather than the statutorily determined formulas. This requirement would
be phased-in starting in 2012. By 2015, MA benchmarks would only be based on a weighted
average of plan bids. This change in the calculation of MA benchmarks could lead to reductions
in benchmarks which in turn could result in reductions in the extra benefits currently received by
MA enrollees, reduced cost sharing, or reduced premiums that some MA plans offer. It may also
impact access to MA plans in some areas.
Several provisions in the amendment would also increase payments to qualifying plans in
qualifying areas of the country. Starting 2014, the amendment would provide bonus payments for
plans that provided care coordination and management activities. Currently, MA plans are
required to have quality improvement programs before January 1, 2010; however, payments to
MA plans are not contingent on the quality of care provided to plan enrollees. Starting in 2014, a
provision would create a second bonus payment for achievement or improvement in plan quality
performance. Other provisions in the amendment would mitigate the reduction in extra benefits
that result from competitive bidding in specified areas or for specified enrollees. Taken together,
the provision to base benchmarks on the bids of MA plans (which may reduce payments to plans)
and the provisions designed to increase payments are estimated to save $34.1 billion over the
FY2010-2014 period and $117.4 billion over the FY2010-2019 period.
In addition, the amendment would extend the Secretary’s authority to adjust payments to plans for
differences in the way diagnosis coding of patients differs between MA plans and original
Medicare. In general, MA plan payments are risk-adjusted to account for the variation in the cost
of providing care. Risk adjustment is designed to compensate plans for the increased cost of
treating older and sicker beneficiaries, and thus discourage plans from preferential enrollment of
healthier individuals. The Deficit Reduction Act of 2005 (P.L. 109-171, DRA) required the
Secretary to adjust for patterns of diagnosis coding differences between MA plans and providers
under parts A and B of Medicare for plan payments in 2008, 2009, and 2010. The amendment
would require the Secretary to conduct further analyses on the differences in coding patterns and
adjust MA plan payments based on the results for 2011, 2012, and 2013. The Secretary would be
granted authority to incorporate results for further analyses for subsequent years. CBO estimates
that this provision would save $1.9 billion over the FY2010-2014 period and $1.9 billion over the
FY2010-2019 period.
The amendment makes additional changes to the Medicare Advantage program that would result
in costs or savings of less than $1.0 billion over the 10-year period (2010-2019), as estimated by
CBO. Each of these provisions is explained in detail in the Appendix.
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Changes Affecting Medicare’s Prescription Drug
Benefit

In January 2010, the Medicare prescription drug program will began its fifth year of operation.
The Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (MMA, P.L. 108-
173) created this voluntary outpatient prescription drug benefit under a new Medicare Part D,
effective January 1, 2006. At that time, Medicare replaced Medicaid as the primary source of drug
coverage for beneficiaries covered under both programs (called dual eligibles). Prescription drug
coverage is provided through private prescription drug plans (PDPs), which offer only
prescription drug coverage, or through Medicare Advantage prescription drug plans (MA-PDs),
which offer prescription drug coverage that is integrated with the health care coverage they
provide to Medicare beneficiaries under Part C. Medicare’s payments to plans are determined
through a competitive bidding process, and enrollee premiums are tied to plan bids. Plans bear
some risk for their enrollees’ drug spending.
Medicare law sets out a defined standard benefit structure under the Part D benefit. In 2009, the
standard benefit includes a $295 deductible and a 25% coinsurance until the enrollee reaches
$2,700 in total covered drug spending. After this initial coverage limit is reached, there is a gap in
coverage in which the enrollee is responsible for the full cost of the drugs (often called the
doughnut hole
) until total costs hit the catastrophic threshold, $6,153.75 in 2009. A major focus of
the drug benefit is the enhanced coverage provided to low-income individuals who enroll in Part
D. Individuals with incomes below 150% of the federal poverty limit and with limited assets are
eligible for the low-income subsidy (LIS). The LIS reduces beneficiaries’ out-of-pocket spending
by paying for all or some of the Part D monthly premium and annual deductible, and limits drug
copayments to a nominal amount.
The Senate Amendment would make several changes to the Medicare Part D program that would
impact beneficiary premiums and out-of-pocket costs. Specifically, the bill would increase Part D
premiums for higher income enrollees; the income thresholds would be set at the same level and
in the same manner as those currently used to establish Part B premiums. Additionally, during the
coverage gap, consistent with a voluntary agreement with the pharmaceutical industry, Part D
enrollees would be provided discounts of 50% for brand name drugs. However, the full drug price
(the amount paid by the beneficiary plus the discount) would be used to calculate a beneficiary’s
out-of-pocket costs. Although this provision would help reduce the out-of-pocket expenditures for
Medicare beneficiaries, CBO scored this provision as a 10-year cost of $19.5 billion to the federal
government.17 This projected cost increase is, in part, based on the expectation that under this
provision a larger number of enrollees would reach the catastrophic phase when Medicare bears
most of the costs, and on the possibility that enrollees who switch from generic to brand name
drugs to take advantage of discounts during the coverage gap may stay on the more expensive
brand name drugs during the catastrophic period.
The amendment also contains several provisions designed to improve access to and availability of
LIS plans. For example, the redetermination of LIS eligibility subsequent to the death of a spouse
would be postponed for a year, and cost sharing would be eliminated for individuals receiving

17 The score for this provision, Section 3301, is combined with the score for Section 3315 which reduces the coverage
gap by $500 in 2010. In its October 7, 2009 analysis of S. 1796, CBO scored the coverage gap discount program alone
at a cost of $17.7 billion over 10 years.
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care under a Medicaid home and community based waiver who would otherwise require care in a
medical institution or a facility. The bill would also make changes to the methodology used to
determine which plans are eligible to enroll low-income beneficiaries so that more plans could
qualify and thus reduce the number of low-income beneficiaries who need to change plans from
year to year. Additional funding would also be provided for outreach and assistance for low-
income programs. The CBO cost estimate for the changes to the low-income subsidy program in
the amendment is $2.4 billion over 10 years.
The Senate amendment also includes a number of provisions aimed at expanding consumer
protections for Part D enrollees. For example, the Secretary would be required to develop and
maintain a centralized system to handle complaints regarding Medicare Advantage and Part
D plans or their sponsors. Additionally, Part D plans would be required to use a single,
uniform exceptions and appeals process.
Efforts to Improve the Efficiency and Quality of
Health Care Services Provided Under Medicare

By statute, Medicare is prohibited from interfering in the practice of medicine or the manner in
which medical services are provided. As such, Medicare pays for virtually all covered products
and services if they are determined to be medically necessary. However, there is growing
evidence that some services provided to Medicare beneficiaries are not medically indicated or are
unnecessary. Additionally, differences in local practice patterns have resulted in substantial
differences in expenditures per beneficiary across geographic areas, but with no measurable
differences in health status.
In June of each year, MedPAC issues a report to Congress that examines systemic issues affecting
the Medicare program and makes recommendations to increase Medicare’s value, to promote its
efficiency, to increase payment accuracy, and/or to realign Medicare’s payment incentives.18 For
instance, MedPAC has concluded that Medicare’s fee-for-service reimbursement system rewards
excessive care and does not encourage service coordination or quality care. Several provisions in
the Senate Amendment are consistent with MedPAC recommendations to provide adequate
incentives to produce appropriate, high-quality care at an efficient price. For example, a provision
included in the Amendment would establish a national, voluntary pilot program that would bundle
payments for physician and hospital as well as post-acute care services with the goal of
improving patient care and reducing spending. Another provision would establish rewards for
accountable care organizations19 that meet quality-of-care targets and reduce costs per patient
relative to a spending benchmark with a share of the savings they achieve for the Medicare
program. CBO estimates that this shared savings program would save Medicare $4.9 billion over
FY2010-2019.
Additionally, under Medicare’s IPPS, acute care hospitals receive a full payment for patient
admissions even if the readmission is preventable and related to the initial admission, the result of

18 MedPAC’s Report to Congress: Improving Incentives in the Medicare Program, June 2009, http://www.medpac.gov/
documents/Jun09_EntireReport.pdf.
19 Defined as groups of providers and suppliers who work together to manage and coordinate care for Medicare fee-for-
service beneficiaries and who meet certain criteria specified by the Secretary.
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inadequate discharge planning at the treating hospital, or results from inadequate post-discharge
care coordination. The Senate Amendment, consistent with MedPAC recommendations, would
adjust payments for hospitals paid under the IPPS based on the dollar value of each hospital’s
percentage of potentially preventable Medicare readmissions for three conditions. The Secretary
of the Department of Health and Human Services would have the authority to expand the policy
to include additional conditions in future years. CBO estimates that this provision would save
$7.1 billion over FY2010-2019. Another provision in the amendment would also subject some
hospitals to a payment penalty under Medicare for certain high-cost and common health
conditions acquired in the hospital. CBO estimates that this provision would result in savings of
$1.5 billion over the next 10 years.
The Senate Amendment would also create a Center for Medicare and Medicaid Innovation within
CMS. The purpose of the center would be to research, develop, test, and expand innovative
payment and delivery arrangements to improve the quality and reduce the cost of care provided to
patients. Successful models could be expanded nationally. CBO estimates that this provision
would lead to an additional savings of $1.3 billion over 10 years.
Changes to Address Medicare Sustainability
Medicare’s financial operations are accounted for through two trust funds, the Hospital Insurance
(HI) trust fund and the Supplementary Medical Insurance (SMI) trust fund, which are maintained
by the Department of the Treasury.20 The primary source of income credited to the HI trust fund,
which finances Medicare Part A, is payroll taxes paid by employees and employers; each pays a
tax of 1.45% on earnings. The trust fund is an accounting mechanism; there is no actual transfer
of money into and out of the fund; rather, income to the trust fund is credited to the fund in the
form of interest-bearing government securities. As long as the trust fund has a balance, the
Treasury Department is authorized to make payments for it from the U.S. Treasury. The 2009
report of the Medicare Board of Trustees, however, projects that the HI trust fund will become
insolvent in 2017.21 If the HI trust fund becomes insolvent, Congress would face a decision of
whether to ensure the continued funding of Medicare Part A, as there is currently no statutory
mechanism that would allow for general fund transfers to cover HI expenditures that exceed
payroll tax income.
Medicare Parts B and D are financed primarily through a combination of monthly premiums paid
by current enrollees and general revenues. Income from these sources is credited to the SMI trust
fund.22 Because the SMI trust fund is funded by annually-adjusted premiums and general revenue
transfers, it is kept in balance and does not face depletion. Growth in SMI expenditures will,
however, require significant increases in beneficiary premiums and general revenue over time.

20 For additional information on Medicare financing see CRS Report RS20173, Medicare: Financing the Part A
Hospital Insurance Program
, by Patricia A. Davis; and CRS Report RS20946, Medicare: History of Part A Trust Fund
Insolvency Projections
, by Patricia A. Davis.
21 2009 Annual Report of the Boards of Trustees of the Federal Hospital Insurance and Federal Supplementary Medical
Insurance Trust Funds, http://www.cms.hhs.gov/reportstrustfunds/.
22 For beneficiaries enrolled in MA, Part C payments are made on their behalf in appropriate portions from the HI and
SMI trust funds.
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In addition to provisions that would reduce annual updates to certain Medicare fee-for-service
payment rates, the Senate Amendment contains several other provisions to address Medicare’s
financial challenges. For example, the Amendment includes a provision to establish an
Independent Medicare Advisory Board to reduce the rate of growth in Medicare spending.
Beginning in 2013, if the Chief Actuary of the Centers for Medicare & Medicaid Services
(OACT) makes a determination that the projected per capita growth rate under Medicare exceeds
certain spending targets in the second year following the determination, the Board is required to
develop a proposal containing recommendations to reduce that per capita growth rate for
submission the following year. The Board would be subject to strict fiscal and policy criteria in
developing its recommendations, including limitations on the types of providers it could target
between years 2015 through 2019. Recommendations made by the Board would be implemented
automatically absent Congressional action. CBO estimates that this provision would save $23
billion between 2015 and 2019.
The Senate Amendment would also impose an additional tax of 0.5% on high-income workers
with wages over $200,000 for single filers and $250,000 for joint filers effective for taxable years
after December 31, 2012. The Joint Committee on Taxation estimates that this provision would
raise $53.8 billion between 2013 and 2019. Another provision in the Amendment would freeze
the income thresholds used to determine which beneficiaries are subject to higher Part B premium
rates at 2010 levels through 2019. Over time, this would result in a larger number of beneficiaries
paying the higher premiums. CBO estimates that this provision would save the Medicare program
$25 billion over 10 years. Additionally, as previously noted, the Senate Amendment would
require high-income Part D prescription drug program enrollees to pay higher premiums. CBO
estimates that this would lead to savings of close to $11 billion over 10 years.
CBO estimated that the Senate Amendment would reduce net Part A outlays by $246 billion over
FY2010-2019.23 As a result of cost reductions and additional revenues raised through increased
payroll taxes, CBO estimates that the HI trust fund would have a positive balance of about $120
billion at the end of FY2019. The balance, however, would still be declining and the HI trust fund
would become insolvent within a few years after 2019.
Changes to Address Fraud, Waste, and Abuse
Health care fraud costs the nation billions of dollars annually. Although the actual amount of
money lost to fraud is unknown, the estimates range from as much as 3% of all health care
expenditures to as much as 10%.24 As health care expenditures continue to rise, developing new
and innovative approaches to fight fraud in both public and private health insurance programs
become increasingly important.

23 http://www.cbo.gov/ftpdocs/107xx/doc10731/Estimated_Effects_of_PPACA_on_HI_TF.pdf.
24 The National Health Care Anti-Fraud Association (NHCAA) estimates conservatively that 3% of all health care
spending—or $68 billion—is lost to health care fraud. The Problem of Health Care Fraud. Available on the NHCAA
website at http://www.nhcaa.org/eweb/DynamicPage.aspx?webcode=anti_fraud_resource_centr&wpscode=
TheProblemOfHCFraud. The Federal Bureau of Investigation (FBI) estimates that as much as 10% of total health care
expenditures could be lost to public and private sector health care fraud. Financial Crimes Report to the Public for
Fiscal Year 2007. Available on the FBI website at http://www.fbi.gov/publications/financial/fcs_report2007/
financial_crime_2007.htm#health.
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As the agency responsible for administering Medicare and Medicaid, the Centers for Medicare
and Medicaid Services (CMS) conducts a variety of activities designed to prevent, detect, and
investigate health care fraud. These activities are referred to as program integrity activities. CMS
shares responsibility for combating health care fraud with three federal agencies: the Department
of Health and Human Services Office of the Inspector General (OIG), the Department of Justice
(DOJ), and the Federal Bureau of Investigation (FBI). The OIG is an independent unit within
HHS that has the primary responsibility for detecting health care fraud and abuse in federal health
care programs. The FBI conducts complex fraud investigations related to both private and public
health care programs, and the OIG, FBI, and CMS refer suspected cases of fraud to the DOJ for
prosecution.
In general, the anti-fraud provisions contained in the Amendment target CMS’s program integrity
activities, the HHS OIG and DOJ enforcement efforts, and funding for anti-fraud activities.
Certain provisions would also apply to the CHIP program. In the area of program integrity, the
legislation would require the Secretary to develop screening procedures for enrolling providers
and suppliers in Medicare, Medicaid, and CHIP. The Secretary would have the authority to
impose background checks, unannounced site visits, enhanced oversight measures, and
moratoriums on enrolling providers. To pay for these screening measures, the legislation would
require providers pay an enrollment fee. Other program integrity measures include requiring
Medicare, Medicaid, and CHIP providers to implement compliance programs, mandating the
expansion of CMS’s payment and claims database, clarifying access to payment and claims data
by law enforcement agencies, and expanding Medicare’s Recovery Audit Contractor (RAC)
program to Medicaid and Medicare Parts C and D.
In the area of enforcement, the legislation introduces new Civil Monetary Penalties (CMPs) for
certain types of infractions, including falsifying information on provider enrollment applications
and delaying investigations and audits by the OIG. The legislation would also enhance the
Secretary’s authority to impose penalties on MA plans for violating the terms of their contract.
Practices such as enrolling individuals into new MA plans or transferring individuals from one
plan to another without consent would be subject to new penalties. Finally, the Senate
Amendment would increase funding for the Health Care Fraud and Abuse Control Program
(HCFAC) by $10 million annually for years 2011 through 2020.
Concluding Observations
Similar to other purchases of health care, Medicare spending has been growing much faster than
the general economy, and concerns about Medicare’s long-term sustainability continue to
intensify. Studies by CBO, MedPAC and others attribute most of the cost growth to the
development and increasing utilization of new treatments and other forms of medical technology.
Although Medicare will have the additional challenge of higher enrollment associated with aging
baby boomers, CBO estimates that most of the expected increase will result from growth in per
capita costs rather than from the aging of the population. The Medicare trustees note that, over
time, the program will require major new sources of financing and impose a significant financial
liability on taxpayers if Medicare benefits and payment systems remain as they are today.
Additionally, Medicare beneficiaries will be responsible for paying for a portion of these rising
expenditures through higher premiums and higher cost sharing.
The Senate Amendment contains provisions designed to reduce Medicare program costs by
approximately $400 billion over the next 10 years through adjustments in payments to certain
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types of providers, by equalizing payment rates between Medicare Advantage and fee-for-service
Medicare, and by increasing efficiencies in the way that health services are paid for and delivered.
There are differing views, however, about whether and to what extent Medicare savings should be
considered as offsets to fund the expansion of health care coverage or, whether these funds are
more appropriately directed at strengthening the program’s future financial standing. Additionally,
Congress confronts a delicate balancing act in weighing the financing issues against the need to
provide and maintain access to appropriate, high quality medical care for Medicare beneficiaries.

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Appendix. Selected Medicare Provisions in the
Senate Amendment (S.Amdt. 2786) in the Nature of
a Substitute to H.R. 3590

This appendix contains the majority of provisions in the proposed legislation affecting the
Medicare program with a brief current law, simplified provision description and, where possible,
the associated CBO score. The section number and title of Medicare provisions that have been
omitted from this appendix will be included in footnotes to the immediately preceding provision.
Title II – Role of Public Programs
Subtitle K—Protections for American Indians and Alaska Natives
Sec. 2902. Elimination of Sunset For Reimbursement for All Medicare Part B Services
Furnished By Certain Indian Hospitals and Clinics.
Medicare covers specified Part B services
provided by, or at the direction of, a hospital or ambulatory care clinic (whether provider-based or
free-standing) that is operated by the Indian Health Service (IHS) and Indian tribe (IT) or a tribal
organization (TO). These services include physician services, health practitioners (physician
assistants, nurse anesthetists, certified nurse-midwives, clinical social workers, clinical
psychologists, and registered dietitians or nutrition professionals) and outpatient physical therapy
services provided by physical or occupational therapists. Section 630 of the Medicare
Prescription Drug, Improvement, and Modernization Act of 2003 (MMA, P.L. 108-173) instituted
a five-year expansion of the items and services covered under Medicare Part B when furnished in,
or at the direction of, IHS, IT, or TO hospitals or ambulatory care clinics, applying to items and
services furnished on or after January 1, 2005. The current five-year reimbursement extension
will expire on January 1, 2010. The provision would amend SSA Sec. 1880(e) (1) (A) to extend
the period for which IHS, IT, and TO services are reimbursed by Medicare Part B indefinitely
beginning January 1, 2010. The CBO score is $0.1 billion for FY2010-FY2014 and is $0.2 billion
for FY2010-FY2019.

Title III – Improving the Quality and Efficiency of Health Care
Subtitle A—Transforming the Health Care Delivery System
Part I – Linking Payment to Quality Outcomes Under the Medicare Program
Sec. 3001. Hospital Value-Based Purchasing Program. Since FY2005, acute care hospitals that
submit required quality data have received higher payments than those hospitals that do not
submit such information under Medicare’s Reporting Hospital Quality Data for Annual Payment
Update (RHQDAPU) program (often referred to as the hospital pay-for-reporting program or P4P
program). There are 46 quality measures collected in the RHQDAPU program that impact the
FY2011 payment update. Individual hospital performance on specific quality measures and on
certain conditions is available on Hospital Compare available on the CMS website. In November,
2007, CMS released a mandated report on the implementation of a Medicare hospital value-based
purchasing (VBP) program, which recommends expanding the RQHDAPU program in order to
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financially reward hospitals differentially for performance; public reporting of performance
would be a key component as well.
Under the Amendment, starting for discharges on October 1, 2012, hospitals would receive value-
based incentive payments from Medicare. The first year of the VBP program would be a data
collection/performance year. Beginning in FY2013, hospital payments would be adjusted based
on performance under the VBP program. Certain hospitals would be excluded from the VBP
program. Acute care hospitals in Maryland paid under their state specific Medicare system would
be exempt if an annual report documents that a similar state program achieves at least comparable
patient outcomes and cost savings. The Secretary would select measures for the hospital VBP
program from those used in the RHQDAPU program. In FY2013, the measures would cover at
least five specified conditions. For discharges occurring during FY2014 and subsequently, the
Secretary would ensure that measures would include appropriate efficiency measures, such as
adjusted Medicare spending per beneficiary.
The Secretary would establish VBP performance standards, including levels of achievement and
improvement, and a methodology for assessing the total performance of each hospital. The
performance standards would be announced no later than 60 days prior to the beginning of the
period. Hospitals with the highest scores would receive the largest VBP payments. There would
not be a minimum performance standard in determining the performance score for any hospital.
Hospitals that meet or exceed the established standards for a performance period would receive
an increased base operating diagnosis-related group (DRG) payment for each discharge in the
fiscal year. Starting in FY2013, the Secretary would fund the VBP incentive payments by
reducing the base operating DRG payments for each hospital’s discharges in a fiscal year by an
applicable percentage. These reductions would apply to all hospitals. The applicable percentage
would be 1.0% in FY2013; 1.25% in FY2014; 1.5% in FY2015; 1.75% in FY2016; and 2.0% in
FY2017 and in subsequent years. Certain adjustments within Medicare’s inpatient hospital
payment system, such as those for outliers, indirect medical education, disproportionate share
hospital and low volume, would not be affected. Certain payments to sole community hospitals
and Medicare dependent hospitals (for FY2012 and FY2013) would also not be affected.
Individual hospital performance on each specific quality measure, on each condition or
procedure, and on total performance would all be publicly reported. A process would be
established that allows hospitals to appeal their performance assessment and score; these appeals
would be resolved in a timely manner. There would be no judicial or administrative review of
certain aspects of the VBP program. The Secretary would consult with small rural and urban
hospitals on the application of the VBP program to such hospitals. The RHAQDPU program
would be modified. The Secretary would be able to require hospitals to submit data on measures
that are not used for the determination of VBP payments. Effective for FY2013 payments, the
Secretary would be required to provide for appropriate risk adjustment for quality measures for
outcomes of care. These measures would be validated appropriately.
The Government Accountability Office (GAO) would conduct a study of the VBP program with
an interim report to Congress due by October 1, 2015 and a final report due by July 1, 2017. The
Secretary would conduct a study of the VBP with a report to Congress due by January 1, 2016.
No later than 2 years from enactment, 3-year, budget neutral VBP demonstration projects would
be established in critical access hospitals (CAHs) and in hospitals excluded from VBP because of
an insufficient volume; reports on the demonstration projects would be due to Congress no later
than 18 months after completion of the projects. The CBO score is $0.0 billion for FY2010-
FY2014 and is $0.0 billion for FY2010-FY2019.

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Sec. 3002. Improvements to the Physician Quality Reporting System. The Tax Relief and
Health Care Act of 2006 (TRHCA, P.L. 109-432) required the establishment of a physician
quality reporting system that would include an incentive payment to eligible professionals who
satisfactorily report data on quality measures, based on a percentage of the allowed Medicare
charges for all such covered professional services. CMS named this program the Physician
Quality Reporting Initiative (PQRI). The Medicare Improvements for Patients and Providers Act
of 2008 (MIPPA, P.L. 110-275) made this program permanent and extended the bonuses through
2010; the incentive payment was increased from 1.5% of total allowable charges under the
physician fee schedule in 2007 and 2008 to 2% in 2009 and 2010.
The proposal would extend PQRI incentive payments through 2014 and implement an incentive
(penalty) for providers who did not report quality measures beginning in 2015. Eligible
professionals who successfully report in 2010 would receive a 1% bonus in 2011; those who
successfully report in 2011, 2012, and 2013 would receive a 0.5% bonus in 2012, 2013, and 2014,
respectively. Subsequently, eligible professionals who failed to participate successfully in the
program would face a 1.5% payment penalty in 2015 and a 2% payment penalty in 2016 and in
subsequent years. The incentive payments and adjustments in payment would be based on the
allowed charges for all covered services furnished by the eligible professional, based on the
applicable percent of the fee schedule amount. The proposal would require CMS to develop a
plan to integrate the PQRI program with the standards for meaningful use of certified electronic
health records as created in the American Recovery and Reinvestment Act of 2009. CBO
estimates that the provision would cost $500 million over FY2010-FY2014 and $100 million over
FY2010-2019; savings would accrue beginning in 2016 and in subsequent years.

Sec. 3003. Improvements to the Physician Feedback Program. MedPAC, GAO and others
have recently recommended providing information to physicians on their resource use. MedPAC
asserts that physicians would be able to assess their practice styles, evaluate whether they tend to
use more resources than their peers or what evidence-based research (if available) recommends,
and revise practice styles as appropriate. MedPAC notes that in certain instances, the private
sector use of feedback has led to a small downward trend in resource use. The GAO noted that
certain public and private health care purchasers routinely evaluate physicians in their networks
using measures of efficiency and other factors and that the purchasers it studied linked their
evaluation results to a range of incentives to encourage efficiency.
MIPPA established a physician feedback program with the intent to improve efficiency and to
control costs. Under the Physician Feedback Program, the Secretary will use Medicare claims
data to provide confidential reports to physicians that measure the resources involved in
furnishing care to Medicare beneficiaries. The resources to be considered in this program may be
measured on an episode basis, on a per capita basis, or on both an episode and a per capita basis.
The GAO will conduct a study of the Physician Feedback Program, including the implementation
of the Program, and will submit a report to Congress by March 1, 2011 containing the results of
the study, together with recommendations for such legislation and administrative action as the
Comptroller General determines appropriate.
The proposal would require new types of reports and data analysis under the physician feedback
program. Not later than January 1, 2012, the Secretary would develop an episode grouper that
combines separate but clinically related items and services into an episode of care for an
individual, as appropriate. Beginning with 2012, the Secretary would provide reports to
physicians that compare patterns of resource use of the individual physician to such patterns of
other physicians.
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In preparing these reports, the Secretary would establish methodologies as appropriate to (i)
attribute episodes of care, in whole or in part, to physicians, (ii) identify appropriate physicians
for purposes of comparison, and (iii) aggregate episodes of care attributed to a physician into a
composite measure per individual. In preparing these reports, the Secretary would make
appropriate adjustments, including adjustments (i) to account for differences in socioeconomic
and demographic characteristics, ethnicity, and health status of individuals, and (ii) to eliminate
the effect of geographic adjustments in payment rates. CBO estimates that this provision would
have no effect on spending over the 5-year or 10-year budget window.

Sec. 3004. Quality Reporting for Long-term Care Hospitals, Inpatient Rehabilitation
Hospitals and Hospice Programs.
Under current law, inpatient rehabilitation facilities (IRFs),
long term care hospitals (LTCHs) and hospices are not required to report quality data to the
Centers for Medicare and Medicaid Services (CMS). Medicare pays for inpatient care provided
by IRFs and LTCHs, and for hospices, using different prospective payment systems (PPS). Each
PPS is updated annually using a market basket (MB) index which measures the estimated change
in the price of goods and services purchased by the provider to produce a unit of output. The
Secretary would be directed to establish quality reporting programs for LTCHs, IRFs, and
hospices. Starting in rate year 2014, LTCHs would be required to submit data on specified quality
measures. This requirement would start in FY2014 for IRFs and hospices. Entities that did not
comply would have a reduction in their annual update of 2 percentage points. The reduction
would be able to result in an annual update that is less than 0.0 which would result in a basis of
payment that is lower than in the preceding year. Any reduction would not affect payments in
subsequent years. The required measures affecting these payments would be published no later
than October 1, 2012. The providers would be able to review the data prior to being publically
available. The CBO score is between -$50 million and +$50 million for FY2010-FY2014 and
-$0.2 billion for FY2010-FY2019.

Sec. 3005. Quality Reporting for PPS-Exempt Cancer Hospitals. Eleven cancer hospitals are
exempt from the Medicare inpatient prospective payment system (IPPS) used to pay inpatient
hospital services provided by acute care hospitals. As part of these exemptions, these facilities are
paid on a reasonable cost basis for providing inpatient services, subject to certain payment
limitations and incentives. Currently, there are no quality reporting requirements for these
hospitals. The Secretary would be directed to establish quality reporting programs for IPPS-
exempt cancer hospitals starting FY2014. These measures would be published no later than
October 1, 2012. The providers would be able to review the data prior to being publically
available. The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-
FY2019

Sec. 3006. Plans for a Value-Based Purchasing Program for Skilled Nursing Facilities
(SNFs) and Home Health Agencies (HHAs).
The Secretary would be required to develop a plan
and submit it to Congress, no later than October 1, 2011, to implement a Medicare value-based
purchasing program for HHAs and SNFs. The plan would be required to consider the following
for each: (1) the development, selection, and modification process of measures, to the extent
feasible and practicable, of all dimensions of quality and efficiency; (2) the reporting, collection,
and validation of quality data; (3) a structure of proposed value-based payment adjustments,
including the determination of thresholds or improvements in quality that would substantiate a
payment adjustment; and (4) methods for publicly disclosing performance information on SNFs.
The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.
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Sec. 3007. Value-Based Payment Modifier Under the Physician Fee Schedule. The Secretary
of Health and Human Services would be required to establish and apply a separate, budget-
neutral payment modifier to the Medicare physician fee schedule. The separate payment modifier
would be based on the relative quality and cost of the care provided by physicians or physician
groups. Quality of care would be evaluated on a composite of risk-adjusted measures of quality
established by the Secretary, such as measures that reflect health outcomes. Costs, defined as
expenditures per individual, would be evaluated based on a composite of appropriate measures of
costs established by the Secretary that eliminate the effect of geographic adjustments in payment
rates and take into account risk factors (such as socioeconomic and demographic characteristics,
ethnicity, and health status of individuals) and other factors determined appropriate by the
Secretary.
By January 1, 2012, the Secretary would publish the specific measures of quality and cost, the
specific dates for implementation of the payment adjustment, and the proposed prospective
performance period. The Secretary would begin implementing the value-based payment
adjustment in the 2013 rulemaking process. During the performance period, which would begin
in 2014, the Secretary would provide information to physicians about the value of care they
provide, as reflected by the measures of relative quality and cost. The Secretary would apply the
payment modifier for items and services furnished beginning on January 1, 2015, for specific
physicians and groups of physicians the Secretary determines appropriate, and not later than
January 1, 2017, for all physicians and groups of physicians. The Secretary would apply the
payment modifier in a manner that promotes systems-based care and takes into account the
special circumstances of physicians or groups of physicians in rural areas and other underserved
communities. CBO estimates that this provision would have no effect on spending over the 5-year
or 10-year budget window.

Sec. 3008. Payment Adjustment for Conditions Acquired in Hospitals. Medicare pays acute
care hospitals using the inpatient prospective payment system (IPPS), where each patient is
classified into a Medicare severity adjusted diagnosis-related group (MS-DRG). Generally, except
for outlier cases, a hospital receives a predetermined amount for a given MS-DRG regardless of
the services provided to a patient. In some instances, Medicare patients may be assigned to a
different MS-DRG with a higher payment rate based on secondary diagnoses. Starting October 1,
2008, hospitals did not receive additional Medicare payment for complications that were acquired
during a patient’s hospital stay for certain select conditions. These hospital acquired conditions
(HACs) are: (1) high cost, high volume, or both; (2) identified though a secondary diagnosis that
will result in the assignment to a different, higher paid MS-DRG; and (3) reasonably preventable
through the application of evidence-based guidelines. Starting for discharges during FY2015,
acute care hospitals in the top quartile of national, risk-adjusted hospital acquired condition
(HAC) rates for an applicable period in a fiscal year would receive 99% of their otherwise
applicable payment. Acute care hospitals in Maryland paid under their state specific Medicare
system would be exempt if an annual report documents that a similar state program achieves at
least comparable quality outcomes and cost savings. Prior to FY2015, the hospitals would receive
confidential reports with respect to their HAC conditions which would be made publicly available
on the Hospital Compare Internet website after the hospital has the opportunity to review and
correct the data. There would be no administrative or judicial review of certain aspects of the
program. The Secretary would submit a report to Congress by January 1, 2012, with
recommendations with respect to expanding Medicare’s HAC payment policy to other facilities,
including IRFs, LTCHs, hospital outpatient departments, inpatient psychiatric facilities, cancer
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hospitals, skilled nursing facilities, ambulatory surgery centers and health clinics. The CBO score
is $0.0 billion for FY2010-FY2014 and -$1.5 billion for FY2010-FY2019.25

Part III – Encouraging Development of New Patient Care Models
Sec. 3021. Establishment of Center for Medicare and Medicaid Innovation Within CMS.
Under the Social Security Act, the Secretary of HHS has broad authority to develop research and
demonstration projects to test new approaches to paying providers, delivering health care
services, or providing benefits to Medicare beneficiaries. This provision would require the
Secretary, no later than January 1, 2011, to establish a Medicare and Medicaid Innovation Center
within CMS. The Innovation Center would test innovative payment and service delivery models
to reduce program expenditures under Medicare, Medicaid, and CHIP while preserving or
enhancing the quality of care furnished to individuals under such titles. In selecting these models,
the Secretary would be required to choose models that also improve the coordination, quality, and
efficiency of health care services furnished to such individuals. The Secretary would be required
to select models that address a defined population for which there are deficits in care leading to
poor clinical outcomes, and may include models which, for example, promote broad payment and
practice reform in primary care; contract directly with groups of providers of services and
suppliers to promote innovative care delivery models; promote care coordination between
providers of services and suppliers that transition health care providers away from fee-for-service
based reimbursement and toward salary-based payment; or utilize medication therapy
management services, among others. The Secretary would not have to require, as a condition for
testing a model under this section, that the model be budget neutral. The Secretary would be
required to conduct an evaluation of each model tested, and make the results of these evaluations
publicly available, including an analysis of (i) the quality of care furnished under the model,
including the measurement of patient-level outcomes; and (ii) the changes in spending under the
applicable titles by reason of the model. This section would also allow the Secretary to expand
the duration and the scope of a model that is being tested under this section or a demonstration
project, if the Secretary determines that such expansion would reduce spending under this title
without reducing the quality of patient care.
This section would authorize to be appropriated, from amounts in the Treasury not otherwise
appropriated, $5 million for the design, implementation, and evaluation of models for FY2010;
$10 billion for the activities under this section for the years 2011 through 2019; and $10 billion
for the activities initiated under this section for each subsequent 10-year fiscal period beginning
with 2020. Beginning in 2012, and not less than once every other year thereafter, the Secretary
would be required to submit to Congress a report on activities under this section. Each such report
would describe: (1) the models tested by the Center, including the number of individuals
participating in such models and payments made under the applicable titles for services on behalf
of such individuals, (2) any models chosen for expansion, and (3) the results from evaluations
under this section. In addition, each such report would provide such recommendations as the
Secretary determines are appropriate for legislative action to facilitate the development and
expansion of successful payment models. The net CBO score on the costs of the center and the

25 Provisions in Part II of Subtitle A of Title III are discussed in CRS Report R40943, Public Health, Workforce,
Quality, and Related Provisions in the Senate Amendment in the Nature of a Substitute to H.R. 3590
, coordinated by C.
Stephen Redhead and Erin D. Williams.

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effect on Medicare spending for benefits is +$0.7 billion for FY2010-FY2014 and -$1.3 billion for
FY2010-FY2019.

Sec. 3022. Medicare Shared Savings Program. In April 2005, CMS initiated the Physician
Group Practice (PGP) demonstration, which offers 10 large practices the opportunity to earn
performance payments for improving the quality and cost-efficiency of health care delivered to
Medicare fee-for-service beneficiaries. Accountable care organizations (ACOs) would go beyond
the PGP model, which is based on physician groups, to include additional providers.
The provision would allow groups of providers who voluntarily meet certain statutory criteria,
including quality measurements, to be recognized as ACOs and be eligible to share in the cost-
savings they achieve for the Medicare program. Beginning no later than Jan. 1, 2012, this shared
savings program would enable eligible ACOs to qualify for an annual incentive bonus if they
achieve a threshold savings amount, established by the Secretary, for total per beneficiary
spending under Medicare parts A and B for those beneficiaries assigned to the ACO. An eligible
ACO would be defined as a group of providers and suppliers who have an established mechanism
for joint decision making, and would be required to participate in the shared savings program for
a minimum of three years, among other requirements. An ACO would include practitioners
(physicians, regardless of specialty; nurse practitioners; physician assistants; and clinical nurse
specialists) in group practice arrangements; networks of practices; and partnerships or joint-
venture arrangements between hospitals and practitioners, among others.
To earn the incentive payment the organization would have to submit data pertaining to quality
and fulfill certain quality requirements related to clinical processes and outcomes, patient and
caregiver experience of care, and utilization measures. The Secretary would have the authority to
adjust the savings thresholds to account for the varying sizes of participating ACOs. If the
Secretary determines that an ACO has taken steps to avoid at-risk patients in order to reduce the
likelihood of increasing costs, the Secretary would be authorized to impose an appropriate
sanction, including terminating agreements with participating ACOs. The CBO score is -$0.5
billion for FY2010-FY2014 and -$4.9 billion for FY2010-FY2019.

Sec. 3023. National Pilot Program on Payment Bundling. As Medicare beneficiaries with
complex health conditions and multiple co-morbidities move between hospital stays and a range
of post-acute care providers, Medicare makes separate payments to each provider for covered
services. The Medicare Payment Advisory Commission (MedPAC), among others, has suggested
that Medicare test new incentives and payment models to encourage providers to better
coordinate across patients’ episodes of care and to evaluate the full spectrum of care a patient may
receive during these episodes.
Under this provision, beginning no later than January 1, 2013, the Secretary would be required to
develop, test and evaluate alternative payment methodologies for Medicare services through a
five-year, national, voluntary pilot program that is designed to provide incentives for providers to
coordinate patient care across the continuum and to be jointly accountable for an entire episode of
care around a hospitalization. Unless otherwise specified by the Secretary, an episode of care
would include the three days prior to a hospital admission for an applicable condition, the hospital
length of stay, and the 30 days following discharge. The pilot program’s bundled payment would
be applicable to one or more of eight conditions and would involve a mix of chronic and acute
conditions, surgical and medical conditions, among others, as selected by the Secretary. The
comprehensive bundled payment would be made to a Medicare provider or other entity
comprised of multiple providers to cover the costs of acute care inpatient and outpatient hospital
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services, physician services delivered in and outside of an acute care hospital setting, and post-
acute services, among others. The payment methodology would also take into account the
provision of care coordination, medication reconciliation, discharge planning and transitional care
services and other patient-centered activities, as determined appropriate by the Secretary.
The bundled payment would comprehensively cover the costs of applicable services and other
appropriate services furnished to an individual during an episode of care (as determined by the
Secretary). Any provider of services and suppliers, including hospitals, physician groups, or post-
acute entities interested in assuming responsibility for the bundled payment would be able to
apply to participate in the pilot program. The Secretary would be directed to establish quality
measures related to the provision of care and to select a patient assessment instrument to evaluate
a beneficiary’s conditions in determining appropriate post-acute care sites. The Secretary would
also be required to conduct an independent evaluation of the pilot program, including an
examination of the extent of performance improvement related to quality measures, health
outcomes, access to care and financial outcomes, and submit reports to Congress no later than
two and three years after date of the implementation of the pilot program. The CBO score is $0.0
billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019
.
Sec. 3024. Independence at Home Demonstration Program. The Secretary would be required
to conduct a Medicare demonstration program, beginning no later than January 1, 2012, to test a
payment incentive and service delivery model that uses physician and nurse practitioner directed
home-based primary care teams designed to reduce expenditures and improve health outcomes in
the provision of items and services to certain chronically ill Medicare beneficiaries. The Secretary
would enter into agreements with qualifying independence at home medical practices, legal
entities comprised of an individual physician or nurse practitioner or group of physicians and
nurse practitioners that provide care as part of a team that includes physicians, nurses, physician
assistants, pharmacists, and other health and social services staff, as appropriate. These practice
staff would have experience providing home-based primary care services to applicable
beneficiaries. Practice staff would make in-home visits, and be available 24 hours per day, 7 days
per week to implement care plans tailored to the individual beneficiary’s chronic conditions and
designed to reduce expenditures and improve health outcomes in the provision of items and
services to applicable beneficiaries.
The Secretary would establish a methodology for sharing savings with independence at home
medical practices that have expenditures below an annual target spending level. The annual
spending target (established by the Secretary) would be the amount the Secretary estimates would
have been spent in the absence of the demonstration, for items and services covered under
Medicare parts A and B provided to applicable beneficiaries. Subject to performance on quality
measures, qualifying practices would be eligible to receive incentive payments if actual annual
expenditures for applicable beneficiaries are less than the estimated spending target. Incentive
payments would be equal to a portion (as determined by the Secretary) of the amount by which
actual expenditures (including incentive payments) would be estimated to be less than 5% less
than the estimated annual spending target.
Agreements with practices under the program could not cover more than a three-year period. The
Secretary would be required to conduct an independent evaluation of the demonstration and
submit to Congress a final report on the demonstration’s best practices and the impact of the pilot
program on coordination of care, expenditures under this provision, access to services, and the
quality of health care services provided to applicable beneficiaries. The Secretary would also be
required to submit a plan, no later than January 1, 2016, for expanding the program if the
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Secretary determines that such expansion would result in improving or not reducing the quality of
patient care and reducing spending under this provision. The provision would appropriate to the
CMS Program Management Account $5 million for each of fiscal years 2010 through 2015 to
administer the demonstration program. The CBO score is between -$50 million and +$50 million
for FY2010-FY2014 and -$0.2 billion for FY2010-FY2019.

Sec. 3025. Hospital Readmissions Reduction Program. Medicare pays for inpatient care
provided by acute care hospitals using an inpatient prospective payment system (IPPS) where
each patient is assigned to a MS-DRG and paid based on an estimate of the average resources
needed to care for a patient with specific diagnoses. Certain atypical cases may qualify for
additional outlier payments. Certain hospitals receive additional indirect medical education (IME)
payments because of their status as a teaching hospital, because they qualify for disproportionate
share hospital (DSH) payments or because they treat a small number (or low volume) of
Medicare patients. Certain types of hospitals that qualify as sole community hospitals (SCHs) or
Medicare dependent hospitals (MDHs) receive additional hospital specific payments. Medicare
pays for inpatient services provided by acute care hospitals in Maryland using a state specific
reimbursement system established under a waiver. Medicare pays for inpatient services in other
types of hospitals such as inpatient rehabilitation facilities (IRFs), inpatient psychiatric facilities
(IPFs), children’s hospitals, and long-term care hospitals using different reimbursement systems.
According to Medicare Payment Advisory Commission’s (MedPAC), in 2005, 6.2% of acute care
hospitalizations of Medicare beneficiaries resulted in readmission within 7 days and 17.6% of
hospitalizations resulted in readmission within 30 days. The 17.6% of hospital readmission
accounted for $15 billion in Medicare spending.
Starting for discharges on October 1, 2012, the Secretary would establish a hospital readmissions
reduction program for certain potentially preventable Medicare inpatient hospital readmissions
covering 3 conditions with high volume or high rate (or both). Medicare’s base operating DRG
payment amounts would be reduced by an adjustment factor. Certain components of Medicare
hospital payments would be exempt from these payment reductions, including outlier, IME, DSH,
and low volume payments. Certain aspects of Medicare’s payments to SCHs and MDHs would be
exempt as well. Acute care hospitals in Maryland would be exempt from these payment
adjustments if a comparable state program achieves the same or higher patient outcomes and cost
savings.
The adjustment factor for a hospital in a fiscal year would be the greater of (1) a floor adjustment
factor equal to a reduced percentage of the discharge payment or (2) the excess readmissions ratio
for the applicable fiscal year. The floor adjustment factor would be 0.99 of the discharge
payments in FY2013, 0.98 of the discharge in FY2014, 0.97 in FY2015 and in subsequent fiscal
years. The excess readmissions ratio would equal 1 minus the ratio of the aggregate payments for
excess readmissions for the hospital divided by the aggregate payments for all discharges. (Each
component of this formula is specified in the provision.) Excess readmissions would include
readmissions over an established minimum number for the specific applicable condition within a
certain period for a hospital.
An applicable condition would be defined as a condition or procedure that represents high volume
(above a minimum threshold) or high expenditures for Medicare or meets other specified criteria
that also satisfies certain measures of readmissions (that have been endorsed by a consensus-
based entity with a performance measurement contract under Section 1890 of the Social Security
Act). Readmissions would not include those readmissions that are unrelated to the prior
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discharge, such as a planned readmission or a transfer to another hospital. Beginning in FY2015,
the number of applicable conditions would be expanded beyond the initial 3 conditions to 4
additional conditions that were identified by MedPAC in its June, 2007, Report to Congress and
other appropriate conditions. These additional conditions would not necessarily need to be
endorsed by a consensus based organization as long as due consideration has been given to such
endorsed or adopted measures.
Readmission information for acute care hospitals would be made publically available after a
hospital has the opportunity to review and correct the data prior to being made public. No judicial
and administrative review would be permitted for certain aspects of the readmission program.
Readmission data for all patients would be submitted by acute care hospitals, IRFs, IPFs,
children’s hospitals, and LTCHs and be made publically available after appropriate review. The
required data would be able to be submitted by a state or other appropriate entity rather than by
each hospital.
No later than 2 years after enactment, a program to improve readmission rates through the use of
patient safety organizations would be established for eligible hospitals. An eligible hospital would
be those with historically high rates of risk adjusted readmissions that have not taken appropriate
steps to reduce readmissions and improve patient safety. Eligible hospitals and patient safety
organizations would report on the processes used to improve readmission rates and resulting
impact on such readmissions. The CBO score is -$0.5 billion for FY2010-FY2014 and -$7.1
billion for FY2010-FY2019.

Sec. 3026. Community-Based Care Transitions Program. Beginning January 1, 2011, the
provision would establish a five-year Community Care Transitions Program under Medicare.
Under this program, the Secretary would fund eligible hospitals (with high admission rates, as
defined under section 3025 of this bill) and certain community-based organizations (that provide
transition services across a continuum of care through arrangements with certain hospitals and
whose governing body includes sufficient representation of multiple health care stakeholders) that
furnish improved care transition services to high-risk Medicare beneficiaries. High-risk Medicare
beneficiaries would refer to beneficiaries who have attained a minimum hierarchical condition
category score, as determined by the Secretary, based on a diagnosis of multiple chronic
conditions or other risk factors associated with a hospital readmission or substandard transition
into post-hospitalizations. Such diagnoses or risk factors could include cognitive impairment,
depression, or a history of multiple readmissions.
Applications by community-based organizations and hospitals to participate in this program
would be required to propose at least one care transition intervention, other than discharge
planning, such as initiating care transition services for targeted high-risk beneficiaries no later
than 24 hours prior to the hospital discharge; arranging timely post-discharge follow-up to
educate patients and, as appropriate, the primary caregiver, about responding to health symptoms
that may indicate additional health problems or a deteriorating condition; among others. In
selecting participating entities, the Secretary would be required to prioritize those entities that
participate in a program administered by the Administration on Aging or provide services to
medically underserved populations, small communities, and rural areas.
A total of $500 million would be transferred by the Secretary from the Federal Hospital Insurance
Trust Fund and the Federal Supplementary Medical Insurance Trust Fund for this program. The
Secretary would have the authority to continue or expand the scope and duration of the program if
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it were determined that quality of care would improve and projected Medicare spending could be
reduced. The CBO score is $0.3 billion for FY2010-FY2014 and $0.5 billion for FY2010-FY2019.
Sec. 3027. Extension of Gainsharing Demonstration. Certain gainsharing demonstrations to
evaluate arrangements between hospitals and physicians have been authorized. CMS is currently
operating two projects, each consisting of one hospital in New York and West Virginia. Although
authorized to begin on January 1, 2007, the project began on October 1, 2008 and will end as
mandated on December 31, 2009. The Secretary was required to submit mandated reports by
certain due dates. The project was appropriated $6 million in FY2006 to be available for
expenditure through FY2010. The authority to conduct the gainsharing demonstration project in
operation as of October 1, 2008 would be extended until September 30, 2011. The due date of the
required interim report would be extended from December 1, 2008, to March 31, 2011 with the
final report due on March 31, 2013. An additional $1.6 million would be appropriated in FY2010;
all appropriations would be available through FY2014 or until expended. The CBO score is
between -$50 million and +$50 million for FY2010-FY2014 and for FY2010-FY2019.

Subtitle B—Improving Medicare for Patients and Providers
Part I – Ensuring Beneficiary Access to Physician Care and Other Services
Sec. 3101. Increase in the Physician Payment Update. Medicare payments for services of
physicians and certain non-physician practitioners are made on the basis of a fee schedule. The
fee schedule assigns relative values to services that reflect physician work (i.e., time, skill, and
intensity it takes to provide the service), practice expenses, and malpractice costs. The relative
values are adjusted for geographic variation in costs. The adjusted relative values are then
converted into a dollar payment amounts by a conversion factor. The law specifies a formula,
commonly referred to as the sustainable growth rate (SGR) formula, for calculating the annual
update to the conversion factors and the resultant fees. Section 101 of the Medicare, Medicaid,
and SCHIP Extension Act of 2007 (MMSEA, P.L. 110-173) increased the update to the
conversion factor for Medicare physician payment by 0.5% compared with 2007 rates for the first
six months of 2008. The Medicare Improvements for Patients and Providers Act of 2008 (MIPPA,
P.L. 110-275) extended the 0.5% increase in the physician fee schedule that was set to expire on
June 30, 2008, through the end of 2008 and set the update to the conversion factor to 1.1% for
2009. The conversion factor for 2010 and subsequent years will be computed as if this
modification had never applied, so unless further legislation is passed, the update formula will
require a 21% reduction in physician fees beginning January 1, 2010 and by additional amounts
annually for at least several years thereafter.
Under this provision, the annual update to the conversion factor used in the determination of the
Medicare fee schedule would be a 0.5% increase in 2010. The conversion factor for 2011 and
subsequent years would be computed as if the increase in 2010 had never applied. CBO estimates
that this provision would cost $7.2 billion in 2010 and $4.1 billion in 2011, with no other
budgetary impact in subsequent years.

Sec. 3102. Extension of the Work Geographic Index Floor and Revisions to the Practice
Expense Geographic Adjustment Under the Medicare Physician Fee Schedule.
The Medicare
fee schedule is adjusted geographically for three factors to reflect differences in the cost of
resources needed to produce physician services: physician work, practice expense, and medical
malpractice insurance. The geographic adjustments are indices—known as Geographic Practice
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Cost Indices (GPCIs)—that reflect how each area compares to the national average in a “market
basket” of goods. A value of 1.00 represents an average across all areas. A series of bills set a
temporary floor value of 1.00 on the physician work index beginning January 2004; most
recently, Section 134 of the MIPPA extended the application of this floor when calculating
Medicare physician reimbursement through December, 2009. The other geographic indices (for
practice expense and medical malpractice) were not modified by these acts.
The proposal would provide a short extension of the floor and introduce a new methodology to
determine the practice expense GPCI. First, the proposal would extend the 1.00 floor for the
geographic index for physician work for an additional year through December 31, 2011. Second,
the proposal would direct the Secretary to adjust the practice expense GPCI for 2010 to reflect 3/4
of the difference between the relative costs of employee wages and rents in each of the different
fee schedule areas and the national averages (i.e., a blend of 3/4 local and 1/4 national) instead of
the full difference under current law. For 2011, the adjustment would reflect 1/2 of the difference
between the relative costs of employee wages and rents in each of the different fee schedule areas
and the national averages (i.e., a blend of 1/2 local and 1/2 national). Relief would apply only to
areas with a practice expense GPCI less than 1.0. The proposal would hold-harmless any areas
negatively impacted by the adjustment.
The proposal would direct the Secretary to analyze current methods of establishing practice
expense geographic adjustments under the physician fee schedule (PE GPCI) and evaluate data
that fairly and reliably establishes distinctions in the costs of operating a medical practice in the
different Medicare payment localities. Based on the analysis and evaluation, the Secretary would
make appropriate adjustments to the PE GPCI to ensure accurate geographic adjustments across
payment areas, no later than January 1, 2012. Adjustments made in 2012 would be made without
regard to the adjustments made in 2010 and 2011. If the Secretary has not completed the required
analysis and evaluation and made appropriate adjustments in the Medicare Physician Fee
Schedule rule for 2012 (or subsequent year), the 2011 payment rule would remain in effect. CBO
estimates that this provision would cost $1.8 billion over the next three years with no further
impact over the remaining years of the 10-year budget window.

Sec. 3103. Extension of Exceptions Process for Medicare Therapy Caps. Current law places
two annual per beneficiary payment limits for all outpatient therapy services provided by non-
hospital providers. For 2009, the annual limit on the allowed amount for outpatient physical
therapy and speech-language pathology combined is $1,840, and there is a separate limit for
occupational therapy of $1,840. The Secretary was required to implement an exceptions process
for 2006, 2007, and the first half of 2008 for cases in which the provision of additional therapy
services was determined to be medically necessary. Section 141 of MIPPA extended the
exceptions process for therapy caps through December 31, 2009. The provision would extend the
exceptions process for therapy caps for an additional year, through December 31, 2010. CBO
estimates that this provision would cost $800 million over the next two years, with no additional
impact over the remaining years of the 10-year budget window.

Sec. 3104. Extension of Payment for Technical Component of Certain Physician Pathology
Services.
In 1999, the Health Care Financing Administration, (now the Centers for Medicare and
Medicaid Services or CMS), proposed terminating an exception to a payment rule that had
permitted laboratories to receive direct payment from Medicare when providing technical
pathology services that had been outsourced by certain hospitals. This exception has been
extended through legislation at various times. Most recently, the Medicare Modernization Act of
2003 (MMA, P.L. 108-173) extended the provision until January 1, 2010. This proposal would
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extend the provision until January 1, 2011. CBO estimates that this provision would cost $100
million in 2010, with negligible or zero costs in future years.

Sec. 3105. Extension of Ambulance Add-ons. Bonus payments were established for ground
ambulance services furnished on or after July 1, 2004 and before January 1, 2010 that originate in
a qualified rural area. The qualified rural areas are those with the lowest population densities that
collectively represent a total of 25% of the population. Subsequently, Medicare rate for ground
ambulance services otherwise established for the year was increased an additional 3% for rural
ambulance services and 2% for other areas for the period July 1, 2008 through December 31,
2009. Areas designated as rural on December 31, 2006 are treated as rural for purposes of
payments for air ambulance services during this period as well. The provision would extend the
bonus payments and the increased ground ambulance payments from April 1, 2010 until January
1, 2011. The provision to pay certain urban air ambulance services as rural was extended from
April 1, 2010 until January 1, 2011, as well. The CBO score is $0.1 billion for FY2010-FY2014
and $0.1 billion for FY2010-FY2019.

Sec. 3106. Extension of Certain Payment Rules for Long-term Care Hospital Services and of
Moratorium on the Establishment of Certain Hospitals and Facilities.
Long-term care
hospitals (LTCHs) are designed to provide extended medical and rehabilitative care for patients
who are clinically complex and have multiple acute or chronic conditions. LTCHs that are distinct
part units of other hospitals are not explicitly permitted by the Medicare statute. Over time,
however, the LTCH industry has evolved to include co-located hospitals-within-hospitals (HwHs)
or satellite facilities in addition to traditional freestanding facilities. CMS has implemented
additional organizational requirements on these LTCHs, in an attempt to ensure that these are
separate entities. Certain LTCHs (grandfathered HwHs) have been exempted from the
requirements. Starting October 1, 2004, CMS established limits on the number of discharged
Medicare patients that an HwHs and satellite LTCHs (except grandfathered LTCHs) can admit
and be paid as independent LTCHs; after that threshold has been reached, generally, the LTCH
will receive a substantially lower payment for subsequent patient admissions who have been
discharged from the host hospital. Starting July 1, 2007, CMS extended this payment policy to
other types of LTCHs, including grandfathered entities. Congress provided for a 3-year
moratorium on the application of this payment policy for certain LTCHs starting December 29,
2007.
Effective for the first cost reporting period beginning on or after October 1, 2002, LTCHs are paid
according to a prospective payment system (PPS), subject to a five-year transition period. By
statute, total payments under LTCH-PPS must be equal to the amount that would have been paid
if the PPS had not been implemented in the initial year of implementation. CMS proposed to
review LTCH payments and make a one-time prospective adjustment to the LTCH PPS to correct
for any errors in the original budget neutrality calculations. The same moratorium was applied to
this policy.
The LTCH-PPS includes certain case level adjustments for short stay and interrupted stay cases.
CMS adopted a very short-stay outlier payment policy starting July 1, 2007 to reduce payments
for patients who have lengths of stay that are less than or equal to one standard deviation from the
geometric average length-of-stay of the same MS-DRG under the IPPS The same moratorium
was applied to this policy. Finally, a 3-year moratorium on new LTCHs, including HwHs and
satellite facilities, and on the increase of hospital beds in existing LTCHs was established.
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The provisions would extend the existing 3-year moratoriums for 1 year until December 29, 2011.
The CBO score is $0.1 billion for FY2010-FY2014 and $0.1 billion for FY2010-FY2019.
Sec. 3107. Extension of Physician Fee Schedule Mental Health Add-On. The Medicare
Improvements for Patients and Providers Act of 2008 (MIPPA, P.L. 110-275) increased payments
for certain Medicare mental health services by 5% beginning on July 1, 2008 and ending on
December 31, 2009. This provision would extend the add-on payment provision through
December 31, 2010. The CBO score is between -$50 million and +$50 million for FY2010-
FY2014 and for FY2010-FY2019.

Sec. 3108. Permitting Physician Assistants to Order Post-Hospital Extended Care Services.
In a skilled nursing facility (SNF), Medicare law allows physicians, as well as nurse practitioners
and clinical nurse specialists who do not have a direct or indirect employment relationship with a
SNF, but who are working in collaboration with a physician, to certify the need for post-hospital
extended care services for purposes of Medicare payment. Section 20.2.1 of Chapter 8 of the
Medicare Benefit Policy Manual defines post-hospital extended care services as services provided
as an extension of care for a condition for which the individual received inpatient hospital
services. Extended care services are considered “post-hospital” if they are initiated within 30 days
after discharge from a hospital stay that included at least three consecutive days of medically
necessary inpatient hospital care.
On or after January 1, 2011, the provision would allow a physician assistant who does not have a
direct or indirect employment relationship with a SNF, but who is working in collaboration with a
physician, to certify the need for post-hospital extended care services for Medicare payment
purposes. The CBO score is between -$50 million and +$50 million for FY2010-FY2014 and for
FY2010-FY2019.

Sec. 3109. Exemption of Certain Pharmacies from Accreditation Requirements. MMA
required the Secretary to establish and implement quality standards for suppliers of durable
medical equipment, prosthetics and supplies (DMEPOS) under Part B of Medicare. MIPPA
requires DMEPOS suppliers to prove their compliance with the quality standards by being
accredited by October 1, 2009. In general, MIPPA exempted specified eligible professionals from
having to comply with the accreditation requirements. Pharmacists and pharmacies are not
exempted from the accreditation requirements. Effective January 1, 2011, the amendment would
exempt certain pharmacies from the accreditation requirements. The CBO score is $0.0 billion for
FY2010-FY2014 and $0.0 billion for FY2010-FY2019
.
Sec. 3110. Part B Special Enrollment Period for Disabled Tricare Beneficiaries. TRICARE,
the health care plan under the Department of Defense (DoD) that covers members of the
uniformed services, their families and survivors, was extended to Medicare-eligible military
retirees, their Medicare-eligible spouses and dependent children and Medicare-eligible
widow/widowers by the Floyd D. Spence National Defense Authorization Act of 2001 (P.L. 106-
398). This law authorized a program known as TRICARE For Life (TFL) which acts as a
secondary payer to Medicare and provides supplemental coverage to TRICARE-eligible
beneficiaries who are entitled to Medicare Part A based on age, disability or end stage renal
disease (ESRD). In order to participate in TFL, these TRICARE-eligible beneficiaries must enroll
in and pay premiums for Medicare Part B. Under Present Law (10 U.S.C. 1086(d)), TRICARE-
eligible beneficiaries who are entitled to Medicare Part A based on age, disability or ESRD, but
decline Part B, lose eligibility for TRICARE benefits. Additionally, individuals who choose not to
enroll in Medicare Part B upon becoming eligible may elect to do so later during an annual
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enrollment period; however, the Medicare Part B late enrollment penalty, would apply. Veterans’
advocacy groups have reported that many beneficiaries are not aware that their TRICARE
coverage is dependent upon Part B enrollment.
This provision would create a twelve-month special enrollment period (SEP) for military retirees,
their spouses (including widows/ widowers) and dependent children, who are otherwise eligible
for TRICARE and entitled to Medicare Part A based on disability or ESRD, but who have
declined Part B. This twelve-month special enrollment period (SEP) would be available to
individuals once in their lifetime and begin on the day after the last day of the initial enrollment
period. Individuals would also have the option of choosing Part B coverage retroactive to the first
month after the initial enrollment period. The late enrollment penalty would not apply to
individuals who enroll during the SEP. The Secretary of Defense would be required to identify
and notify individuals of their eligibility for the SEP; the Secretary of Health and Human Services
and the Commissioner for Social Security would support these efforts. The provision would
become effective on the date of enactment. The CBO score is between -$50 million and +$50
million for FY2010-FY2014 and for FY2010-FY2019.

Sec. 3111. Payment for Bone Density Tests. Dual energy X-ray absorptiometry (DXA) machines
are used to measure bone mass to identify individuals who may have or be at risk of having
osteoporosis. For those individuals who are eligible, Medicare will pay for a bone density study
once every two years, or more frequently if the procedure is determined to be medically
necessary. As reported by CMS and MedPAC, spending for imaging services reimbursed under
the Medicare physician fee schedule grew rapidly between 2003 and 2005. The Deficit Reduction
Act of 2005 (DRA; P.L. 109-171) capped reimbursement of the technical component for x-ray
and imaging services at the lesser rate of the hospital outpatient rate or the physician fee schedule.
Additionally, CMS implemented a new methodology for determining resource-based practice
expense payments for all services that has led to reductions in the professional component
reimbursement. It is estimated that reimbursement rates for DXA services have been reduced
by more than half since 2006. This provision would set payments for DXA at 70% of the 2006
reimbursement rates for these services in 2010 and 2011. The provision would also direct the
Secretary to arrange with the Institute of Medicine of the National Academies to study and report
to the Secretary and Congress on the ramifications of Medicare reimbursement reductions for
DXA on beneficiary access to bone mass measurement benefits. CBO estimates that this
provision would cost $0.1 billion in both FY2010 and FY2011.

Sec. 3112. Revision to the Medicare Improvement Fund. Section 188 of MIPPA established the
Medicare Improvement Fund (MIF), available to the Secretary to make improvements under the
original fee-for-service program under Parts A and B for Medicare beneficiaries. Under current
law, $22.4 billion is available for services furnished during FY2014. The provision would
eliminate the funding in the MIF. The CBO score is -$16.7 billion for FY2010-FY2014 and is
-$22.3 billion for FY2010-FY2019.

Sec. 3113. Treatment of Certain Complex Diagnostic Laboratory Tests. Currently, Medicare
reimbursement for diagnostic laboratory tests performed on specimens collected from a hospital
patient is included in the hospital payment (DRG or outpatient PPS). The proposal would
establish a demonstration project under Medicare part B that would make separate payments to
laboratories for complex diagnostic laboratory tests provided to Medicare beneficiaries.
The term ‘‘complex diagnostic laboratory test’’ would mean a diagnostic laboratory test that is (a)
an analysis of gene protein expression, topographic genotyping, or a cancer chemotherapy
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sensitivity assay, (b) determined by the Secretary to be a laboratory test for which there is not an
alternative test having equivalent performance characteristics, (c) billed using a Health Care
Procedure Coding System (HCPCS) code other than a not otherwise classified code, (d) approved
or cleared by the Food and Drug Administration or is covered under the Medicare program; and
(e) described in section 1861(s)(3) of the Social Security Act (42 U.S.C. 1395x(s)(3)). The term
“separate payment” would mean direct payment to a laboratory (including a hospital-based or
independent laboratory) that performs a complex diagnostic laboratory test on a specimen
collected from a hospital patient if the test is performed after the hospitalization and if a separate
Medicare payment would not otherwise be made.
The demonstration project would run for a 2-year period beginning on July 1, 2011, so long as the
cost of the demonstration program does not exceed $100 million. Not later than 2 years after the
completion of the demonstration project, the Secretary would submit a report to Congress that
would include (1) an assessment of the impact of the demonstration project on access to care,
quality of care, health outcomes, and expenditures or savings to the Medicare program, and (2)
such recommendations as the Secretary would determine to be appropriate. CBO estimates that
this provision would cost $100 million over the next 5 years with no additional impact over the
remaining years of the 10-year budget window.

Sec. 3114. Improved Access for Certified Nurse-Midwife Services. Section 1833 of the SSA
provides for Medicare payments for services received by covered individuals. For certified nurse-
midwife services, the amount required to be paid is 80% of the lesser of either (1) the actual
charge for the services, or (2) the amount determined by a fee schedule established by the
Secretary. The fee schedule is not allowed to exceed 65% of the prevailing charge that would be
allowed for the same services performed by a physician. This provision would amend Section
1833 by adding that for services provided on or after January 1, 2011, the fee schedule for
certified-midwife services would not be allowed to exceed 100% of the fee schedule amount
provided under Section 1848 for the same service performed by a physician. The CBO score is
between -$50 million and +$50 million for FY2010-FY2014 and for FY2010-FY2019.

Part II – Rural Protections
Sec. 3121. Extension of Outpatient Hold Harmless Provision. Small rural hospitals (with no
more than 100 beds) that are not sole community hospitals (SCHs) can receive additional
Medicare payments if their outpatient payments under the prospective payment system are less
than under the prior hospital outpatient department (HOPD) reimbursement system. For calendar
year (CY) 2006, these hospitals received 95% of the difference between payments under the
prospective payment system and those that would have been made under the prior reimbursement
system. The hospitals receive 90% of the difference in CY2007 and 85% of the difference in
CY2008 and CY2009. Sole community hospitals with not more than 100 beds receive 85% of the
payment difference for covered HOPD services furnished on or after January 1, 2009, and before
January 1, 2010. The provision would establish that small rural hospitals would receive 85% of
the payment difference in CY2010. SCHs with not more than 100 beds would receive 85% of the
payment difference in CY2010. The 100-bed limitation for SCHs would be removed so that all
SCHs would receive 85% of the payment difference in CY2010. The CBO score is $0.2 billion
for FY2010-FY2014 and $0.2 billion for FY2010-FY2019.

Sec. 3122. Extension of Medicare Reasonable Costs Payments for Certain Clinical
Diagnostic Laboratory Tests Furnished to Hospital Patients in Certain Rural Areas.
Generally, hospitals that provide clinical diagnostic laboratory services under Part B are
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reimbursed using a fee schedule. Hospitals with under 50 beds in qualified rural areas (certain
rural areas with low population densities) receive 100% of reasonable cost reimbursement for the
clinical diagnostic laboratories covered under Part B that are provided as outpatient hospital
services. Reasonable cost reimbursement for laboratory services provided by these hospitals
ended July 1, 2008. Reasonable cost reimbursement for clinical diagnostic laboratory service for
qualifying rural hospitals with under 50 beds would be reinstated from July 1, 2010 and extended
for one year, ending July 1, 2011. The CBO score is between -$50 million and +$50 million for
FY2010-FY2014 and for FY2010-FY2019.

Sec. 3123. Extension of the Rural Community Hospital Demonstration Program. CMS is
conducting a five-year Rural Community Hospital Demonstration Program to test the feasibility
and advisability of reasonable cost reimbursement for small rural hospitals (those with fewer than
51 beds) in low population density areas. No more than 15 hospitals can participate in the
demonstration. Currently, there are 10 hospitals participating in the program. This provision
would extend the demonstration program for an additional year, expand the maximum number of
participating hospitals to 30 for that period, and specify that the 20 states with low population
densities would participate in the demonstration project. The Secretary would provide for the
continued participation for those hospitals that are in the demonstration at the end of the initial 5-
year period during the 1-year extension unless the hospital elects to discontinue such
participation. The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-
FY2019.

Sec. 3124. Extension of the Medicare-dependent Hospital (MDH) Program. Medicare
dependent hospitals (MDHs) are small rural hospitals with a high proportion of patients who are
Medicare beneficiaries. Specifically, the hospitals have at least 60% of acute inpatient days or
discharges attributable to Medicare in FY1987 or in 2 of the 3 most recently audited cost
reporting periods. As specified in regulation, they cannot be a sole community hospital and must
have 100 or fewer beds. MDHs receive special treatment, including higher payments, under
Medicare’s inpatient prospective payment system. The sunset date for the MDH classification has
been periodically extended by legislation and is presently set to expire September 30, 2011. The
MDH classification would be extended one year, until September 30, 2012. The CBO score is
between -$50 million and +$50 million for FY2010-FY2014 and for FY2010-FY2019.

Sec. 3125. Temporary Improvements to the Medicare Inpatient Hospital Payment
Adjustment for Low-Volume Hospitals.
Under Medicare’s inpatient prospective payment
system (IPPS), certain low-volume hospitals receive a payment adjustment to account for their
higher costs per discharge. A low-volume hospital is defined as an acute care hospital that is
located more than 25 road miles from another comparable hospital and that has less than 800 total
discharges during the fiscal year. Under current law, the Secretary is required to determine an
appropriate percentage increase for these low-volume hospitals based on the empirical
relationship between the standardized cost-per-case for such hospitals and their total discharges to
account for the additional incremental costs (if any) that are associated with such number of
discharges. The low-volume adjustment is limited to no more than 25%. Accordingly, under
regulations, qualifying hospitals (those located more than 25 road miles from another comparable
hospital) with less than 200 total discharges receive a 25% payment increase for every Medicare
discharge. A temporary adjustment that would increase payment in FY2011 and FY2012 for
certain low-volume hospitals would be created. A low volume hospital could be located more
than 15 road miles from another comparable hospital and have 1,500 discharges of individuals
entitled to or enrolled for Medicare Part A benefits. The Secretary would determine the applicable
percentage increase using a continuous linear sliding scale ranging from 25% for low-volume
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hospitals with 200 or fewer discharges of individuals with Medicare Part A benefits to no
adjustment for hospitals with greater than 1,500 discharges of individuals with Medicare Part A
benefits. The CBO score is $0.3 billion for FY2010-FY2014 and $0.3 billion for FY2010-FY2019.
Sec. 3126. Improvements to the Demonstration Project on Community Health Integration
Models in Certain Rural Counties.
A demonstration project to allow eligible entities to develop
and test new models for the delivery of health care services in eligible counties has been
authorized. Those eligible to participate in the demonstration project are limited to certain entities
in States with at least 65% of its counties in the State with 6 or fewer residents per square mile.
Based on these criteria, the Secretary is instructed to select up to 4 states to participate in the
demonstration program, and within those states, up to 6 counties. For a county to be eligible to
participate, it must have 6 or fewer residents per square mile and contain a critical access hospital
(CAH) that furnished one or more of specified services (home health, hospice, or rural health
clinic) and had a daily inpatient census of 5 or less as of date of enactment; skilled nursing facility
services must be available in the eligible county. The 3-year demonstration project is to begin on
October 1, 2009 and be done in a budget neutral manner. The provision would eliminate the limit
of 6 eligible counties that may participate in the demonstration project within the qualifying
states. Rural health clinic services would no longer be one of specified CAH services. Rural
health clinic services would be removed from the definition of other essential services and
replaced with physician services. The CBO score is $0.0 billion for FY2010-FY2014 and $0.0
billion for FY2010-FY2019.

Sec. 3127. MedPAC Study on Adequacy of Medicare Payments for Health Care Providers
Serving in Rural Areas.
MedPAC would be required to review payment adequacy for rural
health care providers and suppliers serving the Medicare program and provide a report to
Congress by January 1, 2011. MedPAC would analyze rural payment adjustments, beneficiaries’
access to care in rural communities, adequacy of Medicare payments to rural providers and
suppliers, and quality of care in rural areas, and submit a report to Congress by January 1, 2011.
The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.
Sec. 3128. Technical Correction Related to Critical Access Hospital Services. Critical Access
Hospitals (CAHs) are limited-service rural facilities that meet certain distance criteria; offer 24-
hour emergency care; have no more than 25 acute care inpatient beds and have a 96-hour average
length of stay. Generally, a rural hospital designated as a CAH receives 101% reasonable, cost
based reimbursement for inpatient and outpatient care rendered to Medicare beneficiaries. A CAH
may elect an all-inclusive outpatient payment which is equal to a 101% of reasonable costs for
facility services plus 115% of the Medicare physician fee schedule payment for professional
services when the physician or practitioner has reassigned his or her billing rights to the CAH. As
part of its FY2010 rulemaking process, starting October 1, 2009, CMS will lower the facility
component of the all-inclusive, elective payment method from 101% to 100% of the CAH’s
reasonable costs; the payment for professional services will remain at 115% of the fee schedule
amount. Medicare pays for ambulance services provided by a CAH or by an entity owned and
operated by a CAH at 100% of reasonable costs, but only if CAH or the entity is the only supplier
or provider of ambulance services with a 35-mile drive of the CAH or the entity.
Under this provision, Medicare would pay the facility component of the all-inclusive elective
CAH payment for outpatient services at 101% of reasonable costs. Medicare would pay for
qualifying ambulance services provided by a CAH or by an entity owned and operated by a CAH
at 101% of reasonable cost. The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion
for FY2010-FY2019.

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Sec. 3129. Extension of and Revisions to Medicare Rural Hospital Flexibility Program. One
component of the Medicare Rural Hospital Flexibility Program is a grant program (FLEX grants)
that is administered by the Health Resources and Services Administration (HRSA). Under this
program, Flex grants may be awarded to States and to small rural hospital for certain purposes.
There are certain limitations imposed on the use of grant funds for administrative expenses, both
at the state and Federal level. The FLEX grant program is authorized at $55 million for each
fiscal year from 2009 and 2010 and the new rural mental health and other services grants would
be authorized at $55 million for each of fiscal years 2009 and 2010. The FLEX grant program
would be extended two years until 2012. Starting January 1, 2010, grant funding would be
available to be used to assist small rural hospitals to participate in delivery system reforms. The
CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

Part III – Improving Payment Accuracy
Sec. 3131. Payment Adjustments for Home Health Care. Home health agencies (HHAs) are
paid under a prospective payment system (PPS) that provides payments based on 60-day episodes
of care for beneficiaries, subject to several adjustments. The base payment amount of the PPS is
adjusted for differences in the care needs of patients (case mix) using “HH resource groups”
(HHRGs) and outlier adjustments (to account for extraordinarily costly patients), among other
adjustments. Presently, there is no difference between urban and rural base payment amounts.
In CY2008, refinements to the Medicare HH PPS included, among other changes, a reduction in
the payment rate for 4 years (to continue through CY2011) to adjust for increases in case mix that
are related to changes in coding instead of increased patient severity of illness. The proposed
CMS rule for CY 2010 would continue with the 2.75% reduction to the HH PPS rates for CY
2010. Among other things, the proposed rule would also implement a cap on outlier payments to
be no more than 2.5% of total HH PPS payments.
Starting in CY2013, the Secretary would be directed to rebase home health payments by a
percentage considered appropriate by the Secretary to, among other things, reflect the number,
mix and level of intensity of HH services in an episode, and the average cost of providing care. In
doing so, the Secretary could consider the differences between HH agencies in regards to
hospital-based and freestanding providers; for-profit and non-profit providers; and resource costs
between urban and rural providers. Any such adjustments that would result would be required to
be made before the next HH market basket payment update. A four-year phase-in, ending in 2016,
would be provided for, in equal increments that could not exceed 3.5% of applicable amounts for
each year.
Starting in CY2011, the Secretary would be directed to establish a provider-specific annual cap of
ten percent of revenues that a HH agency may be reimbursed in a given year from outlier
payments. For visits ending on or after Apri1 1, 2010 and before January 1, 2016, the Secretary
would be directed to provide for a three percent add-on payment for HH providers serving rural
areas. The CBO score is -$5.4 billion for FY2010-FY2014 and -$42.1 billion for FY2010-FY2019.
Sec. 3132. Hospice Reform. For a person to be considered terminally ill for eligibility purposes
for Medicare’s hospice benefit, the beneficiary’s attending physician and the medical director of
the hospice (or physician member of the hospice team) must certify that the individual has a life
expectancy of six months or less. The medical director or physician member of the hospice team
must recertify that the beneficiary is terminally ill at the beginning of each 90- or 60-day
eligibility period. Medicare payments to hospices are predetermined fixed daily amounts for each
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case, and are based on one of four prospectively determined units of payment, which correspond
to four different levels of care (i.e., routine home care, continuous home care, inpatient respite
care, and general inpatient care).
Under the provision, Secretary would be required to begin, by January 1, 2011, collecting
additional data and information needed to revise payments for hospice care. Not earlier than
October 1, 2013, the Secretary would be required to, by rulemaking, implement budget neutral
revisions to the methodology for determining hospice payments for routine home care and other
services that could include per diem payments to hospices reflecting differences in resources used
or additional payments (end-of-episode payment) reflecting resource intensity of services
provided at the end of episode, among others.
In addition, the provision would require the Secretary to impose new requirements on hospice
providers that participate in Medicare, including requiring, on or after January 1, 2011, that (1) a
hospice physician or advanced practice nurse have a face-to-face encounter with the individual
regarding eligibility and recertification and attest that hospice visits are made; and (2) stays in
excess of 180 days, that meet certain conditions, be medically reviewed by CMS or its
contractors. The CBO score is between -$50 million and +$50 million for FY2010-FY2014 and
for FY2010-FY2019.

Sec. 3133. Improvement to Medicare Disproportionate Share Hospital (DSH) Payments.
Medicare’s disproportionate share hospital (DSH) adjustment was included in the inpatient
prospective payment system (IPPS) in 1986 on the premise that low-income patients are more
costly to treat and those acute care hospitals serving a large number of such patients would be
likely to have higher costs for their Medicare patients than would otherwise similar institutions.
Over time, as the formulas for Medicare’s DSH adjustment have been changed, the justification
for the higher payments has evolved and the adjustment is viewed as a way to insure access to
hospital care. Medicare’s DSH payments are distributed through a hospital-specific percentage
increase to its prospective payment rate. In most instances, the size of a hospital’s DSH
adjustment would depend upon the number of patient days provided to poor Medicare patients or
Medicaid patients. In its March 2007 Report to Congress, MedPAC found that about three-
quarters of the Medicare DSH payments (accounting for about $5.5 billion in FY2004) was not
empirically justified in terms of higher patient care costs. Also, Medicare’s DSH payments were
poorly targeted to hospitals’ shares of uncompensated care
Starting in FY2015 and for subsequent fiscal years, the Secretary would make DSH payments
equal to 25% of what otherwise would be made, a payment that represents the empirically
justified amount as determined by MedPAC in its March 2007 Report to Congress. In addition to
this amount, starting in FY2015, the Secretary would pay to such acute care hospitals an
additional amount using a formula that is the product of 3 factors: the difference in the hospital’s
DSH payments because of this legislation; the difference in the percentage change in the
uninsured under-65 population from 2012; and the percentage of uncompensated care provided
by the hospital (relative to all acute care hospitals). There would be no administrative or judicial
review of certain aspects of this payment policy. The CBO score is $0.0 billion for FY2010-
FY2014 and -$20.6 billion for FY2010-FY2019.

Sec. 3134. Misvalued Codes Under the Physician Fee Schedule. The Medicare physician fee
schedule is based on assigning relative weights to each of the more than 7,000 physician service
codes used to bill Medicare. The relative value for a service compares the relative work involved
in performing one service with the work involved in providing other physicians’ services. The
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scale used to compare the value of one service with another is known as a resource-based relative
value scale (RBRVS). CMS is responsible for maintaining and updating the fee schedule,
including the modification and refinement of the methodology for estimating relative value units
(RVUs). CMS relies on advice and recommendations from the American Medical
Association/Specialty Society Relative Value Scale Update Committee (RUC) in its assessments.
In general, as currently implemented, increases in RVUs for a service or number of services
lowers the resultant fees for other physician services because of the budget neutrality condition.
One consequence has been that the payments for evaluation and management codes, whose RVUs
typically are not increased over time, have fallen relative to other codes whose RVUs have
increased and as a consequence of new technologies that have been introduced into coverage with
relatively high RVUs. CMS is required to review the RVUs no less than every five years.
The Secretary would be required to periodically identify physician services as being potentially
misvalued, and make appropriate adjustments to the relative values of such services under the
Medicare physician fee schedule. To identify potentially misvalued services, the Secretary would
examine codes (and families of codes as appropriate) with the fastest growth, that have
experienced substantial changes in practice expenses, for new technologies or services, that are
frequently billed in conjunction with furnishing a single service, with low relative values,
particularly those that are often billed multiple times for a single treatment, that have not been
subject to review since the implementation of the RBRVS (the so-called ‘Harvard-valued codes’),
and other codes the Secretary determined to be appropriate. The Secretary would review and
make appropriate adjustments to the work relative value units under the fee schedule.
The provision would repeal Section 4505(d) of the Balanced Budget Act of 1997, which
established requirements for developing new resource-based practice expense relative value units,
as well as Section 1868(a) of the Social Security Act (42 U.S.C. 1395ee(a)), which established the
Practicing Physicians Advisory Council, a group of physicians who meet quarterly to discuss
proposed changes in regulations and carrier manual instructions related to physician services.
CBO estimates that this provision would have no impact on spending over the 5-year or 10-year
budget window.

Sec. 3135. Modification of Equipment Utilization Factor for Advanced Imaging Services.
Under the Medicare fee schedule, some services have separate payments for the technical
component and the professional component. For example, imaging procedures generally have two
parts: the actual taking of the image (the technical component), and the interpretation of the
image (the professional component). Medicare pays for each of these components separately
when the technical component is furnished by one provider and the professional component by
another. When both components are furnished by one provider, Medicare makes a single global
payment that is equal to the sum of the payment for each of the components.
CMS’s method for calculating the Medicare fee schedule reimbursement rate for advanced
imaging services assumed that imaging machines are operated 25 hours per week, or 50% of the
time that practices are open for business. Setting the equipment use factor at a lower rate has led
to higher payment for these services. Citing evidence showing that the utilization rate is 90%,
rather than the 50% previously assumed, MedPAC is urging CMS to use the higher utilization rate
in the calculation of fee schedule payments for advanced imaging services.
The proposal would change the utilization rate assumption for calculating the payment for
advanced imaging equipment from 50% to 65% for 2010 through 2012. The rate would be further
increased to 70% for services provided in 2013 and 75% for services provided in 2014.
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According to MedPAC and the Government Accountability Office (GAO), there are opportunities
to improve the efficiency of the Medicare fee schedule. In 2005, MedPAC recommended
reducing certain fees to account for efficiencies and savings from the technical preparation and
supplies achieved when multiple imaging services are furnished sequentially on contiguous body
parts during the same visit. Starting January 1, 2006, physicians receive the full technical
component fee for the highest paid imaging service in a visit, but technical component fees for
additional imaging services are reduced by 25%. The proposal would increase the technical
component payment reduction for sequential imaging services on contiguous body parts during
the same visit from 25% to 50%. By January 1, 2013, the CMS Chief Actuary would conduct and
make publicly available an analysis of whether the cumulative expenditure reductions attributable
to these adjustments are projected to exceed $3 billion for the period 2010 through 2019. The
CBO score is -$1.1 billion for FY2010-FY2014 and -$3.0 billion for FY2010-FY2019.

Sec. 3136. Revision of Payment for Power-Driven Wheelchairs. Medicare pays for new or
replacement power-driven wheelchairs either through monthly rental payments during the
beneficiary’s period of medical need (not to exceed 13 continuous months), or, on a lump-sum
basis. Rental payments for wheelchairs are statutorily determined as 10% of the purchase price of
the chair for each of the first 3 months and 7.5% of the purchase price for each of the remaining
10 months of the rental period. Medicare pays for most DME on the basis of a fee schedule,
except in Competitive Acquisition Areas where payments are to be determined based on supplier
bids. Starting January 1, 2011, the provision would restrict the lump-sum payment option for new
or replacement chairs to only the complex, rehabilitative power wheelchairs. The lump-sum
payment option would be eliminated for all other wheelchairs. The provision would not apply to
competitive acquisition areas prior to January 1, 2011. Also starting January 1, 2011, the rental
payment for power-driven wheelchairs would be 15% of the purchase price for each of the first
three months (instead of 10%), and 6% of the purchase price for each of the remaining 10 months
of the rental period (instead of 7.5%). The CBO score is -$0.6 billion for FY2010-FY2014 and
-$0.8 billion for FY2010-FY2019
.
Sec. 3137. Hospital Wage Index Improvement. A hospital wage index is used to adjust the
standardized amount to account for the local wage variation or cost of labor in the hospital’s area.
Starting in FY2005, CMS has adjusted this data to account for the relative skill mix of the
hospitals in the area. This occupationally mix adjusted average hourly wage is then divided by the
same measure calculated using data from all hospitals in the nation to establish the area’s adjusted
wage index. MedPAC issued its mandated report on recommended changes to the hospital wage
index in June 2007. CMS has hired an independent consulting firm to further evaluate the impact
of making the recommended changes.
Unlike other providers, acute care hospitals may apply to the Medicare Geographic Classification
Review Board (MGCRB) for a change in classification from a rural area to an urban area, or
reassignment from one urban area to another urban area. To reclassify, a hospital had to meet
certain standards, establishing that its average hourly wage (AHW) was within a certain threshold
of the AHW of the area where it wanted to reclassify. Starting in FY2010, CMS raised the
reclassification threshold. MGCRB hospital reclassifications are established on a budget neutral
basis so aggregate inpatient payments will not increase as a result of the reclassified hospitals’
higher payments.
Section 508 of the Medicare Prescription Drug, Improvement and Modernization Act of 2003
(MMA, P.L. 108-173) provided $900 million for a one-time, three year geographic
reclassification of certain hospitals who were otherwise unable to qualify for administrative
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reclassification to areas with higher wage index values. These reclassifications were extended
legislatively at various points until September 30, 2009
This provision would extend the Section 508 reclassifications until September 30, 2010. The
Secretary would be required to use the FY2010 wage index data throughout the extension. By
December 31, 2011, the Secretary would be required to provide a plan to Congress on how to
comprehensively reform the Medicare wage index system; this plan would take into account
MedPAC recommendations included in its June 2007, Report to Congress. The Secretary would
also be required to restore the reclassifications thresholds used in determining hospital
reclassifications to the percentages used for FY2009 MGCRB decisions, starting in FY2011 and
in subsequent fiscal years (until the first fiscal year beginning on or after the date that is one year
after the date of the submission of the Secretary’s wage index reform plan). This provision would
be implemented in a budget neutral fashion. The CBO score is $0.2 billion for FY2010-FY2014
and $0.2 billion for FY2010-FY2019.

Sec. 3138. Treatment of Certain Cancer Hospitals. Eleven cancer hospitals are exempt from
the inpatient prospective payment system (IPPS) used to pay inpatient hospital services provided
by acute care hospitals. These hospitals are also held harmless under the outpatient prospective
payment system (OPPS) and will not receive less from Medicare under this payment system than
under the prior outpatient payment system. Under OPPS, Medicare pays for outpatient services
using ambulatory payment classification (APC) groups. This provision would require the
Secretary to conduct a study which would consider the cost of drugs and biologics to determine if
the outpatient costs incurred by IPPS-exempt cancer hospitals with respect to Medicare’s APCs
exceed those costs incurred by other hospitals reimbursed under OPPS. If so, the Secretary would
be required to provide for an appropriate OPPS adjustment starting January 1, 2011. The CBO
score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

Sec. 3139. Payment for Biosimilar Biological Products. A biologic is a preparation, such as a
therapeutic product or a vaccine, which is made from living organisms. Medicare Part B pays for
a limited number of drugs and therapeutic products, including biologics, administered to patients
in physician offices and hospital outpatient departments, or those administered through durable
medical equipment (DME) and billed by pharmacy suppliers. CMS assigns a Healthcare
Common Procedure Coding System (HCPCS) code to each drug, and Medicare payments for Part
B drugs are based on the average sales price (ASP) for each HCPCS code. CMS uses the same
HCPCS code for all drug products listed as therapeutically equivalent in FDA’s Orange Book.
Therefore, a brand-name drug and any generic versions of the same drug would have the same
HCPCS code and the prices would be averaged together for ASP determinations. The provision
would allow a Part B biosimilar product approved by the Food and Drug Administration to be
reimbursed at the ASP of the biosimilar plus six percent of the ASP of the reference product. (The
term reference biological product means the licensed biological product that is referred to in the
application for the biosimilar product.) This provision assumes the enactment of Title VII of this
amendment that would expand the regulatory activities of FDA by opening a pathway for the
approval of biosimilars.26 The CBO score (Sections 3139 and Sections 7001-7003 combined) is
-$0.1 billion for FY2010-FY2014 and -$7.1 billion for FY2010-FY2019.


26 Sections 7001-7003 in Subtitle A of Title VII on biologic price competition and innovation are discussed in CRS
Report R40943, Public Health, Workforce, Quality, and Related Provisions in the Senate Amendment in the Nature of a
Substitute to H.R. 3590
, coordinated by C. Stephen Redhead and Erin D. Williams.

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Sec. 3140. Medicare Hospice Concurrent Care Demonstration Program. Medicare covers
hospice care for terminally ill beneficiaries instead of most other Medicare services related to the
curative treatment of their illness. The provision would require the Secretary to conduct a three-
year demonstration program, from Medicare funds that would otherwise be paid for hospice care,
to allow patients who are eligible for hospice to also receive all other Medicare covered services
during the same period of time. The Secretary would select not more than 15 hospice programs in
both urban and rural areas to examine improvement in patient care, quality of life, and cost-
effectiveness that results from the demonstration project. The CBO score is between -$50 million
and +$50 million for FY2010-FY2014 and for FY2010-FY2019.

Sec. 3141. Application of Budget Neutrality on a National Basis in the Calculation of the
Medicare Hospital Wage Index Floor for Each All-Urban and Rural State.
A hospital wage
index is used to adjust the standardized amount to account for the local wage variation or cost of
labor in the hospital’s area. As required by statute, the wage index for any urban area in a state
cannot be less than the rural wage index of that state (often referred to as the rural floor). The
effect of the rural floor (that is, raising the wage index for urban areas in a state to that state’s
rural wage index) is required to be implemented on a budget neutral basis by adjusting the wage
index of all hospitals not affected by the rural floor. Until FY2009, CMS funded the budget
neutrality requirement associated with the impact of the rural floor though a nationwide
adjustment. Starting in FY2009, CMS began a transition to fund the budget neutrality
requirement through a state-specific adjustment; the statewide adjustment would be fully
implemented in FY2011. States with no hospitals receiving the rural floor wage index would not
have a reduced payment; those hospitals within each state with urban areas paid at the higher
rural wage index would fund the higher payments for the affected hospitals. The proposal would
require application of budget neutrality requirement associated with the effect of the imputed
rural and rural floor on a national basis (through a uniform, national adjustment to the area wage
index). The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.
Sec. 3142. HHS Study on Urban Medicare-Dependent Hospitals. Medicare dependent
hospitals (MDHs) are small rural hospitals with a high proportion of patients who are Medicare
beneficiaries. MDHs receive special treatment, including higher payments, under Medicare’s
inpatient prospective payment system (IPPS). Certain other hospitals, such as rural referral
centers (RRC) and sole community hospitals (SCHs) receive special treatment under IPPS. Other
small, limited service critical access hospitals (CAHs) are exempt from IPPS and paid 101% of
their reasonable costs. IPPS includes certain payment adjustments, such as the indirect medical
education (IME) adjustment for teaching hospitals, to compensate hospitals for higher average
costs which might not be in their control. The disproportionate share hospital (DSH) adjustment
increases payments for hospitals that serve a relatively high proportion of poor Medicare and
Medicaid patients. This provision would require the Secretary to conduct a study within 9 months
of enactment on the need for an additional Medicare payments for urban Medicare-dependent
hospitals paid under IPPS which receive no additional IPPS payments (have an IME or DSH
adjustment) or receive special treatment (as an RRC, SCH, or MDH). CAHs would be excluded
as well. The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.
Subtitle C—Provisions Relating to Part C
Sec. 3201. Medicare Advantage Payment. Medicare Advantage (MA) is an alternative way for
Medicare beneficiaries to receive covered benefits. Under MA, private plans are paid a per-person
amount to provide all Medicare-covered benefits (except hospice) to beneficiaries who enroll in
their plan. Payments to MA plans are determined by comparing plan bids to a benchmark. Each
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bid represents the plan’s estimated revenue requirement for providing required Medicare services
to an average Medicare beneficiary. The benchmark is the maximum amount Medicare will pay a
plan. If the plan bid is below the benchmark, the plan payment is the bid plus a rebate equal to
75% of the difference between the bid and the benchmark. If the bid is above the benchmark, the
plan is paid the benchmark and each plan enrollee must pay a premium equal to the difference
between the bid and the benchmark. MA benchmarks are based, in part, on historical Medicare
private plan payment rates. (MA benchmarks for Regional MA plans are based in part on
historical MA plan payments, and in part on Regional MA plan bids.) Benchmark amounts are
increased each year by the growth in Medicare spending (the national MA per capita growth
percentage), or in certain years, the benchmark may be set at the greater of the previous year’s
rate increased by the growth in Medicare or average spending in original Medicare in that area,
with adjustments. Local MA plans choose the counties they wish to serve. Regional plans must
serve an entire region defined by the Secretary, and may choose to serve more than one region.
Regions are made up of states or groups of states. Though all MA organizations are required to
have a quality improvement program by January 1, 2010, payments to MA plans are not
contingent on the quality of care provided to plan enrollees.
Under the proposal:
MA Benchmarks and Rebates. In 2011, the national MA per capita growth percentage used to
increase benchmarks would be reduced by three percentage points. Starting in 2012, the proposed
law would phase-in MA benchmarks based on a weighted average of plan bids. In 2012, local MA
benchmarks would be based on 33% of the enrollment weighted average of plan bids for each
payment area and 67% of the current law MA benchmarks. By 2015, the MA local benchmarks
would be determined by the enrollment weighted average of MA bids in each payment area.
Local benchmarks would be prohibited from exceeding the levels that would have existed under
current law. Regional plan benchmarks would continue to be calculated as a weighted blend of
the regional bids and local MA benchmarks. However, the local benchmark portion of the
regional benchmark would be based on the new competitively bid MA benchmarks. Beginning in
2014, the MA plan rebates would be increased from 75% of the difference between the bid and
the benchmark, to 100% of the difference. For bids submitted on or after January 1, 2012, the
proposed law would require bid information to be certified by a member of the American
Academy of Actuaries, in addition to other specified requirements.
Payment Areas. Beginning in 2012, the Secretary would establish new MA payment areas for
urban areas based on Core Based Statistical Area (CBSA). CBSAs that crossed state boundaries
would be divided into separate payment areas. The Secretary would have authority to adjust
CBSA-based payment areas and exempt certain plans from the requirements. MA plans would be
allowed to choose which payment areas to serve, but would be required to bid and serve the entire
payment area, and would no longer be allowed to apply different premiums to different segments
within their service area.
Bonus Payments. Starting in 2014, the amendment would establish two new bonus payments for
local and regional MA plans – a care coordination and management bonus and a quality bonus.
The value of the bonuses would be based on specified percentages of the national per capita
monthly cost for individuals enrolled under the original Medicare program (hereafter “national
expenditures”). Under the care coordination and management bonus, plans would be able to earn
0.5% of “national expenditures” for each of 8 specified programs with a maximum of 2.0% of
“national expenditures” possible. The quality bonus program would be based on a plan’s absolute
quality or improvement in quality. Quality would be measured using a 5-star rating system, or a
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similar system. Plans that receive at least a 3-star rating would receive 2% of “national
expenditures”; plans that receive a 4- or 5-star rating would receive 4% of “national
expenditures.” Plans that did not achieve at least a three-star rating would be eligible for a one
percent quality bonus if their ratings improve over a prior year. Additional quality bonuses would
be available for new plans, and low-enrollment plans.
Grandfather Policy. MA plans would be allowed to grandfather extra benefits for their current
enrollees (as of enactment) in certain areas of the country where average bids were not greater
than 75% of local fee-for-service costs in 2009. Plans would be able to grandfather enrollees
beginning in 2012. The amount of extra benefits would be reduced by 5% each year beginning in
2013.
Transitional benefits. Starting in 2012, the Secretary would provide for transitional rebates for
extra benefits to specified enrollees. This provision would apply to beneficiaries who enroll in an
MA local plan and experiences a significant reduction of benefits as a result of competitive
bidding. The policy would apply to (1) the two largest metropolitan statistical areas if the total
amount of extra benefits for each enrollee for the month in those areas was greater than $100, or
(2) a county where the MA benchmark amount in 2011 was equal to the legacy urban floor
amount, the Medicare Advantage enrollment penetration was greater than 30% in 2011, and the
average of MA plan bids was below local fee-for-service costs, with adjustments. The total
amount available for transitional benefits would be $5 billion through 2019.
The CBO score (combined with Section 3209) is -$34.4 billion for FY2010-FY2014 and -$118.1
billion for FY2010-FY2019
.
Sec. 3202. Benefit Protection and Simplification. Under MA, enrollee cost sharing (i.e.,
coinsurance, copayments, and deductibles) is determined on a plan-by-plan basis. Cost sharing
for a particular service may be greater than or less than the cost sharing under original Medicare,
and may change from year to year. However, the total value of cost sharing required by an MA
plan is constrained by the estimated actuarial value of total cost sharing under original Medicare.
Under the amendment, beginning in 2011, MA plans would be prohibited from charging cost
sharing that is greater than the cost sharing under original Medicare for certain services including
chemotherapy treatment, renal dialysis, skilled nursing care, and services identified by the
Secretary. Beginning in 2012, the amendment would restrict plans’ authority to apportion their
rebates and bonus payments between additional benefits, reduced cost sharing and reduced
premiums. MA plans would have to apply the full amount of rebates, bonuses, and supplemental
premiums according to the following priority order: (1) reduction of cost sharing, (2) coverage of
preventive and wellness benefits, and (3) other benefits not covered under original Medicare. MA
plans would be prohibited from reducing or eliminating the Part B premium as an additional
benefit. The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.
Sec. 3203. Application of Coding Intensity Adjustment During MA Payment Transition.
Medicare payments to MA plans are risk-adjusted to account for the variation in the cost of
providing care. DRA required the Secretary to adjust for patterns of diagnosis coding differences
between MA plans and providers under parts A and B of Medicare for plan payments in 2008,
2009, and 2010, to the extent that the Secretary identified such differences. The Secretary did not
make adjustments in 2008 and 2009, due to ongoing analyses, but is to adjust rates in 2010. The
amendment would require the Secretary to conduct an analysis of the differences in coding
patterns between MA and original Medicare and incorporate the results of the analysis into risk
scores for 2011, 2012, and 2013. The Secretary would be granted authority to incorporate the
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results of further analyses for subsequent years. The CBO score is -$1.9 billion for FY2010-
FY2014 and -$1.9 billion for FY2010-FY2019
.
Sec. 3204. Simplification of Annual Beneficiary Election Periods. Medicare beneficiaries may
enroll in or change their enrollment in MA from November 15 to December 31 each year (the
annual, coordinated election period). Changes go into effect January 1st of the next year. During
the first 3 months of the year, beneficiaries can enroll in an MA plan, and individuals enrolled in
an MA plan can either switch to a different MA plan or return to original Medicare (the
continuous open enrollment and disenrollment period). Effective beginning in 2011, the
amendment would shift the annual, coordinated election period for MA and Part D to October 15
through December 7. Also beginning in 2011, the amendment would prohibit beneficiaries from
switching MA plans or enrolling in an MA plan from original Medicare after the start of the
benefit year. The amendment would, however, allow beneficiaries who had enrolled in Medicare
Advantage during the annual, coordinated election period to disenroll and return to original
Medicare during the first 45-day period of the new benefit year (January 1-February 15), and
allow those beneficiaries to enroll in a Part D prescription drug plan. The CBO score is between
-$50 million and +$50 million for FY2010-FY2014 and for FY2010-FY2019.
Sec. 3205. Extension for Specialized MA Plans for Special Needs Individuals. The Medicare
Prescription Drug, Improvement, and Modernization Act of 2003 (MMA, P.L. 108-173)
established a new type of Medicare Advantage (MA) coordinated care plan focused on
individuals with special needs. Special needs plans (SNPs) are allowed to target enrollment to one
or more types of special needs individuals including 1) institutionalized; 2) dually eligible; and/or
3) individuals with severe or disabling chronic conditions. This provision of the Amendment
would extend SNP authority through December 31, 2013. The Secretary would be required to
establish a frailty payment adjustment, similar to PACE, for fully-integrated dual-eligible SNPs.
The Secretary would only have authority to adjust payments to dual-eligible SNP when those
plans had fully integrated Medicare and Medicaid benefits, including long-term care, and met
other criteria. Fully-integrated dual-eligible SNPs would be exempted from the IME payment
phase-out applicable to all MA plans.
In addition, the provision would temporarily extend authority through the end of 2012 for SNPs
that do not have contracts with state Medicaid programs to continue to operate, but not to expand
their service area. The proposal would require the Secretary to establish a process to transition
SNP beneficiaries that do not qualify as special needs individuals, to fee-for-service Medicare and
other MA plans. As part of the transition process, the Secretary would provide for an exception
process for beneficiaries who lose Medicaid coverage to reapply for benefits. Beginning in 2012,
SNPs would be required to have approval of the National Committee for Quality Assurance in
order to serve targeted populations. Periodically, beginning in 2011, the Secretary would be
required to evaluate, revise, and publish the MA risk adjustment payment methodology to
recalibrate payments for higher medical and care coordination costs for specified conditions. The
CBO score (combined with Section 3208) is $0.7 billion for FY2010-FY2014 and $0.9 billion for
FY2010-FY2019
.
Sec. 3206. Extension of Reasonable Cost Contracts. Reasonable cost plans are Medicare
Advantage (MA) plans that are reimbursed by Medicare for the actual cost of providing services
to enrollees. Cost plans were created in the Tax Equity and Fiscal Responsibility Act (TEFRA) of
1982. The Balanced Budget Act of 1997 included a provision to phase-out the reasonable cost
contracts, however, the phase-out has been delayed over the years through Congressional action.
These plans are allowed to operate indefinitely, unless two other plans of the same type (i.e.,
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either 2 local or 2 regional plans) offered by different organizations operate for the entire year in
the cost contract’s service area. After January 1, 2010, the Secretary may not extend or renew a
reasonable cost contract for a service area if: (a) during the entire previous year there were either
two or more MA regional plans or two or more MA local plans in the service area offered by
different MA organizations; and (b) these regional or local plans meet minimum enrollment
requirements. The amendment would extend for three years—from January 1, 2010, to January 1,
2013—the length of time reasonable cost plans may continue operating regardless of any other
MA plans serving the area. The CBO score is between -$50 million and +$50 million for FY2010-
FY2014 and for FY2010-FY2019.

Sec. 3207. Technical Correction to MA Private Fee-for-Service Plans. MA coordinated care
plans are required to meet medical access requirements by forming networks of contracted
providers. Prior to 2011, PFFS plans can meet medical access requirements either by establishing
payment rates for providers that are not less than rates paid under original Medicare or by
developing contracts and agreements with a sufficient number and range of providers within a
category to provide covered services under the terms of the plan. Starting in 2011, PFFS plans
sponsored by employers or unions are required to establish contracted networks of providers to
meet access requirements. Non-employer sponsored MA PFFS plans are required to establish
contracted networks of providers in “network areas” defined as areas having at least two plans
with networks (such as health maintenance organizations [HMOs], provider sponsored
organizations [PSOs], or local preferred provider organizations [PPOs]). In areas without at least
two network-based plans, the non-employer PFFS plans retain the ability to establish access
requirements through establishing payment rates that are not less than those under original
Medicare.
This provision would allow the Secretary to grant employer-based PFFS plans a waiver from the
network requirements in a manner similar to the Secretary’s authority to waive or modify other
MA requirements for employer-based coordinated care plans as specified in a 2008 service area
extension waiver policy, as modified in an April 11, 2008 CMS memo entitled “2009 Employer
Group Waiver-Modification of the 2008 Service Area Extension Waiver Granted to Certain MA
Local Coordinated Care Plans.” The CBO score is $0.1 billion for FY2010-FY2014 and $0.1
billion for FY2010-FY2019
.
Sec. 3208. Making Senior Housing Facility Demonstration Permanent. In general, MA plans
are required to serve an area no smaller than a county, which prevents plans from targeting
smaller areas of healthier, low-cost enrollees. However, it is possible for an MA plan to receive a
waiver of this requirement to be able to restrict enrollment to residents of a retirement
community. Effective January 1, 2010, the amendment would create a new type of MA plan
called an MA Senior Housing Facility Plan, which would be allowed to limit its service area to a
senior housing facility within a geographic area. An MA Senior Housing Facility Plan would be
an MA plan that serves beneficiaries who reside in a continuing care retirement community, has a
sufficient number of on-site primary care providers as determined by the Secretary, supplies
transportation benefits to other providers, and were in existence under a demonstration for at least
one year. The CBO score for this section was included in the estimate for Section 3205.
Sec. 3209. Authority to Deny Plan Bids. In general, the Secretary has the authority to negotiate
bids submitted by MA plans similar to the authority of the Director of the Office of Personnel
Management with respect to negotiations with plans participating in the Federal Employees
Health Benefits Program. The Secretary may only accept a bid after determining that it is
supported actuarially and that it reasonably and equitably reflects the revenue requirements of
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benefits provided under the plan. The Secretary’s authority to negotiate with plans does not apply
to Private Fee-for-Service (PFFS) MA plans. Effective January 1, 2011, the amendment would
clarify that the Secretary is not required to accept any or every bid submitted by an MA plan or
Part D prescription drug plan. The CBO score for this section was included in the estimate for
Section 3201.

Sec. 3210. Development of New Standards for Certain Medigap Plans. Many Medicare
beneficiaries have individually purchased health insurance policies, commonly referred to as
“Medigap” policies. Beneficiaries with Medigap insurance typically have coverage for
Medicare’s deductibles and coinsurance; they may also have coverage for some items and
services not covered by Medicare. Individuals generally select from one of a set of standardized
plans (Plan “A” through Plan “L”, though not all plans are offered in all states). The law
incorporates by reference, as part of the statutory requirements, certain minimum standards
established by the National Association of Insurance Commissioners (NAIC) and provides for
modification where appropriate to reflect program changes. The provision would request that
NAIC create new model plans for C and F that include nominal cost sharing to encourage the use
of appropriate Part B physician services. The nominal cost sharing would be based on evidence
either published or from integrated delivery systems. The revisions would be consistent with rules
applicable to changes in NAIC Model Regulations. The new models C and F would be available
in 2015. The CBO score is $0.0 billion for FY2010-FY2014 and -$0.1 billion for FY2010-
FY2019
.
Subtitle D—Medicare Part D Improvements for Prescription Drug Plans and
MA-PD Plans

Sec. 3301. Medicare Coverage Gap Discount Program for Brand-Name Drugs. This
provision incorporates a voluntary agreement with the Pharmaceutical Research and
Manufacturers of America (PhRMA) to provide discounts of 50% for brand-name drugs used by
Part D enrollees in the Part D coverage gap. Manufacturers of prescription drugs would enter into
agreements with Medicare Part D drug plan sponsors to provide discounts on drugs provided to
plan enrollees in the coverage gap period. The amount of the discount, in addition to the amount
actually paid by the enrollee, would count toward costs incurred by the plan enrollee. Plan
enrollees receiving the low income subsidy, enrolled in an employee–sponsored retiree drug plan,
or have annual incomes that exceeds the Part B income thresholds as determined under current
law ($85,000 for singles and $170,000 for couples in 2009) would not be eligible for the discount.
Drugs sold and marketed in the U.S. by a manufacturer would not be covered under Part D unless
the manufacturer agrees to participate in the discount program. The provision would also require
the Secretary to contract with a third party entity (or entities) to administer the drug discount
program and would establish performance requirements and data standards for the third-party
contractor(s). This provision would be applicable to drugs dispensed beginning July 1, 2010. The
CBO score (combined with Sec. 3315) is +$7.4 billion for FY2010-FY2014 and +$19.5 billion
for FY2010-FY2019.

Sec. 3302. Improvement in Determination of Part D Low-Income Benchmark Premium. The
federal government pays up to 100% of the Part D premiums for low-income subsidy (LIS)
beneficiaries who are enrolled in “benchmark” plans. A Part D plan qualifies as a benchmark plan
if it offers basic Part D coverage with premiums equal to or lower than the regional low-income
premium subsidy amount. MA plans offering prescription drug coverage submit a separate bid for
the Part D portion. Payment for the portion of the premium attributable to basic prescription drug
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benefits is calculated in the same way as that for stand-alone PDPs, however an MA plan may
choose to apply some of its Part C rebate payments to lower the Part D premium. If an MA plan
uses rebate payments to reduce its Part D premium, this reduced amount is factored into the
calculation of the regional low-income benchmark. This has the effect of lowering the benchmark
and potentially of reducing the number of plans that qualify as low-income plans. MedPAC has
noted that the number of plans that qualify as low-income benchmark plans has been decreasing
in recent years, resulting in fewer options for LIS enrollees. This provision would exclude the
Medicare Advantage rebate amounts from the MA-PDP premium bids when calculating the low-
income regional benchmark for subsidy determinations made. The provision would take effect in
2011. The CBO score is +$0.3 billion for FY2010-FY2014 and +$07 billion for FY2010-FY2019.
Sec. 3303. Voluntary De Minimus Policy for Subsidy Eligible Individuals Under
Prescription Drug Plans and MA-PD Plans.
To help maintain plans that wish to serve LIS
beneficiaries at fully subsidized or $0 premiums, this provision would authorize a policy,
beginning in 2011, through which plans that bid a nominal amount above the regional low-
income subsidy (LIS) benchmark amount could choose to absorb the cost of the small difference
between their bid and the LIS benchmark in order to qualify as a LIS-eligible plan. The Secretary
would be given discretion to auto-enroll LIS beneficiaries into these plans in order to maintain
adequate LIS plan choices. The de minimus threshold amount would be established by the
Secretary. The CBO score is +$0.1 billion for FY2010-FY2014 and +$0.4 billion for FY2010-
FY2019.

Sec. 3304. Special Rule for Widows and Widowers Regarding Eligibility for Low-Income
Assistance.
To qualify for financial assistance under the Part D low-income subsidy (LIS)
program, Medicare beneficiaries must have resources no greater than the income and resource
limits established by the Medicare Prescription Drug, Improvement, and Modernization Act of
2003 (MMA, P.L. 108-173). Each year, the Secretary conducts a redeeming process to determine
whether those who automatically qualified for the full subsidy in a given year continue to meet
the criteria for eligibility in the following year. For those who have qualified for the full or partial
subsidy through the application process, the agency that made the determination decision (SSA or
an individual state) is responsible for monitoring a recipient’s eligibility. For example, for cases in
which eligibility has been established through an application with SSA, a report of a subsidy-
changing event, such as marriage, divorce, or death of a spouse, will trigger a redetermination of
subsidy eligibility during the calendar year. This can result in changes to the individual’s
deductible, premium and cost sharing subsidy, or even termination of his or her LIS eligibility
status. In the case of the death of a spouse, it is possible that the surviving spouse, as the sole
owner of the previously combined resources, may exceed the resource limit for an individual and
may no longer qualify for the LIS program.
The proposal would require that, beginning in 2011, the surviving spouse of an LIS-eligible
couple undergo a redetermination of his or her eligibility status no earlier than one year from the
next redetermination that would have occurred after the death of a spouse. Subsequently, the LIS
widow/widower would be determined or redetermined, as appropriate, for LIS on the same basis
as other LIS-eligible beneficiaries. The CBO score is +$0.1 billion for FY2010-FY2014 and
+$0.2 billion for FY2010-FY2019.

Sec. 3305. Improved Information for Subsidy Eligible Individuals Reassigned to
Prescription Drug Plans and MA-PD Plans.
According to the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA, P.L. 108-173), low-income subsidy (LIS)
beneficiaries who are enrolled in plans with premiums below the low-income regional benchmark
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amount receive assistance with premiums and cost sharing. Those who are enrolled in LIS-
eligible plans whose plan bids exceed the regional benchmark amount for the next benefit year
are randomly reassigned by the Secretary of HHS to new plans whose bids are at or below the
regional benchmark amount in order to ensure that these beneficiaries continue to receive a
subsidy of plan premiums. It is possible that the new plan’s exceptions, appeals and grievance
mechanisms could differ from the old plan and that some covered drug(s) a beneficiary is
currently taking would not be covered by the new plan.
In the case of an LIS beneficiary who has been reassigned to another LIS plan, the provision
would require the Secretary, beginning in 2011 to transmit within 30 days of the reassignment,
information to the beneficiary about formulary differences between the former plan and the new
plan with respect to the beneficiary’s drug regimen, as well as a description of the beneficiary’s
rights to request a coverage determination, exception or reconsideration, or resolve a grievance.
The CBO score is between -$50 million and +$50 million for FY2010-FY2014 and for FY2010-
FY2019.

Sec. 3306. Funding Outreach and Assistance for Low-Income Programs. Section 119 of the
Medicare Improvements for Patients and Providers Act of 2008 (MIPPA, P.L. 110-275) provided
$25 million for fiscal years 2008 and 2009 for beneficiary outreach and education activities
related to low-income programs related to the Medicare through State Health Insurance
Counseling and Assistance Programs (SHIPs), Area Agencies on Aging (AAAs), Aging and
Disability Resource Centers (ADRCs), and the Administration on Aging (AoA). This provision
would extend MIPPA Section 119 and provide an additional $45 million for outreach and
education activities related to Medicare low-income assistance programs, including the Part D
low-income subsidy (LIS) program and the Medicare Savings Program (MSP). Funds would be
allocated to SHIPs, AAAs, ADRCs, and the National Center for Benefits Outreach and
Enrollment in the same proportion as under MIPPA and would be available for obligation through
2012. The Secretary would also be provided the authority to enlist the support of these entities to
conduct outreach activities aimed at preventing disease and promoting wellness as an additional
use of these funds. The CBO score is between -$50 million and +$50 million for FY2010-FY2014
and for FY2010-FY2019.

Sec. 3307. Improving Formulary Requirements for Prescription Drug Plans and MA-PD
Plans with Respect to Certain Categories or Classes of Drugs.
The Medicare Prescription
Drug, Improvement, and Modernization Act of 2003 (MMA, P.L. 108-173) requires Part D plans
to operate formularies that cover drugs within each therapeutic category and class of covered Part
D drugs, although not necessarily all drugs within such categories and classes. The Secretary of
HHS published a regulation (42 CFR Section 423.120) that requires Part D plans to have at least
two drugs within each therapeutic category and class. However, through sub-regulatory guidance,
the Secretary protected access to certain classes of drugs by requiring Part D plans to cover all, or
substantially all, of the drugs in the following six drug classes: immunosuppressant,
antidepressant, antipsychotic, anticonvulsant, antiretroviral, and anti-neoplastic. Section 176 of
the Medicare Improvements for Patients and Providers Act of 2008 (MIPPA, P.L. 110-275)
codified that, beginning in plan year 2010, the Secretary would identify the classes and categories
of drugs that should be protected, or covered entirely by Part D plans, to ensure that beneficiaries
have access to certain therapies and to a wide variety of therapy options for certain conditions and
established certain criteria the Secretary would use to identify such drugs.
The proposal would give the Secretary authority to identify classes of clinical concern as defined
by the Secretary and PDP sponsors would be required to include all drugs in these classes in their
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formularies. The proposal would also codify the current six classes of clinical concern as they are
currently specified through sub-regulatory guidance until the Secretary issues a rule regarding
classes of clinical concern to be protected on plan formularies. The proposed law would also
remove the criteria specified in Section 176 of MIPPA that would have been used by the
Secretary to identify protected classes of drugs. The provision would be effective for the 2011
plan year. The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-
FY2019.

Sec. 3308. Reducing Part D Premium Subsidy for High-Income Beneficiaries. Beginning in
2007, as required by the MMA, high-income beneficiaries are required to pay higher premiums
for Part B benefits. Beneficiaries with modified adjusted gross income that exceeds a threshold
amount are charged additional premiums based on a sliding scale that ranges from 35 percent to
80 percent of the value of Part B. In 2009, threshold levels started at $85,000 for an individual tax
return and $170,000 for a joint return (based on 2007 returns). The threshold amounts are
specified in the law, and are adjusted annually for inflation using the Consumer Price Index
(CPI). The income thresholds are tied to specific premium shares. Beneficiary premiums under
Part D are not subject to income thresholds or means testing. This provision would require Part D
enrollees who exceed certain income thresholds to pay higher premiums. The income thresholds
would be set in a similar manner to those under Part B. The provision would also inflate the
income thresholds by the CPI, except for the period between 2010 and 2019 when the income
thresholds would not be updated. In addition, the provision would expand the current authority
for IRS to disclose income information to SSA for purposes of adjusting the Part B subsidy to
include the Part D subsidy adjustments. The CBO score is -$2.4 billion for FY2010-FY2014 and
-$10.7 billion for FY2010-FY2019.

Sec. 3309. Elimination of Cost Sharing for Certain Dual Eligible Individuals. Cost-sharing
subsides for LIS enrollees are linked to the standard Part D prescription drug coverage. Full-
subsidy eligibles have no deductible, minimal cost sharing during the initial coverage period and
coverage gap, and no cost-sharing over the catastrophic threshold. Full-benefit dual eligibles who
are residents of medical institutions or nursing facilities have no cost-sharing. This provision
would eliminate cost sharing for drugs dispensed on or after January 1, 2011 for people receiving
care under a home and community based waiver who would otherwise require institutional care.
The CBO score is +$0.3 billion for FY2010-FY2014 and +$1.1 billion for FY2010-FY2019.
Sec. 3310. Reducing Wasteful Dispensing of Outpatient Prescription Drugs in Long-Term
Care Facilities Under Prescription Drug Plans and MA-PD Plans.
Part D plans are required to
offer a contract to any pharmacy willing to participate in its long-term care (LTC) pharmacy
network so long as the pharmacy is capable of meeting certain minimum performance and service
criteria and any other standard terms and conditions established by the plan for its network
pharmacies. Each LTC facility selects at least one eligible LTC pharmacy to provide Medicare
drug benefits to its residents. Plan formularies must be structured so that they meet the needs of
long-term care residents and provide coverage for all medically necessary medications at all
levels of care. Both physician prescribing patterns and pharmacy benefit manager (PBM)
payment practices result in prescriptions commonly being dispensed in 30- or 90-day quantities.
In situations when the full amount dispensed is not utilized by the patient, for example. due to
discharge, death, adverse reactions, the remaining medication may become waste. This provision
would require Part D sponsors, starting January 1, 2012, to employ utilization management
techniques, determined by the Secretary in consultation with relevant stakeholders, to reduce the
quantity dispensed per fill when dispensing medications to beneficiaries who reside in long-term
care facilities in order to reduce waste associated with 30-day fills. These techniques could
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include such things as weekly, daily, or automated dose dispensing. The CBO score is -$1.0
billion for FY2010-FY2014 and -$5.7 billion for FY2010-FY2019.

Sec. 3311. Improved Medicare Prescription Drug Plan and MA-PD Complaint System. Part
D and Medicare Advantage (MA) related complaints are tracked and resolved through a
centralized complaints system within the Centers for Medicare & Medicaid Services (CMS),
while complaints submitted directly to plan sponsors (grievances) are tracked and resolved by
each plan sponsor using its own system. CMS maintains a central repository of MA and Part D-
related complaints received by its Regional Offices, Central Office, or through 1-800-
MEDICARE. This provision would require the Secretary to develop and maintain a system,
which is widely known and easy to use, to handle complaints regarding MA and Part D plans or
their sponsors. The system would have the ability to report and initiate appropriate interventions
and monitoring based on substantial complaints and to guide quality improvement. A plan
complaint would be defined as a complaint that is received (including by telephone, letter, e-mail,
or any other means) by the Secretary (including by a regional office, the Medicare Beneficiary
Ombudsman, a sub-contractor, a carrier, a fiscal intermediary, or a Medicare Administrative
Contractor). The Secretary would be required to develop a model electronic complaint form to be
used for reporting complaints under the system that would be displayed on the Medicare.gov and
Medicare Beneficiary Ombudsman websites. The Secretary would also be required to conduct
annual reports of the complaint system that would include an analysis of the numbers and types of
complaints reported under the system; geographic variations in the complaints; the timeliness of
agency or plan responses to the complaints; and the resolution of the complaints. The CBO score
is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

Sec. 3312. Uniform Exceptions and Appeals Process for Prescription Drug Plans and MA-
PD Plans.
Section 1852(g) of the Social Security Act outlines general requirements regarding
Medicare Advantage exceptions and appeals processes. The Part D program adapted many of the
existing rules for appeals that apply to Medicare Advantage program. The coverage and
determination and appeals processes may vary among MA and Part D plans as long as these
general requirements are met. This provision would require a prescription drug plan sponsor or a
MA organization offering MA-PD plans to use a single, uniform exceptions and appeals process
with respect to the determination of prescription drug coverage for an enrollee under the plan and
to provide instant access to this process through a toll-free telephone number and an Internet
website. This provision would apply to exceptions and appeals made on or after January 1, 2012.
The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.
Sec. 3313. Office of the Inspector General Studies and Reports. According to Section 1860D-
14 of the SSA, full-benefit dual-eligible individuals who have not elected a Part D plan are to be
auto-enrolled into one by CMS. Because plans vary in the formularies they offer, some dual
eligibles could find that they have been auto-enrolled in a plan that may not best meet their needs.
Additionally, when the Medicare prescription drug program was created, it was expected that
drug plan sponsors would negotiate with drug manufacturers to obtain price concessions on drugs
covered under Part D, and thus reduce total costs to the government and to beneficiaries. Some
studies have suggested that Part D plans are not obtaining rebates equivalent to those required
under Medicaid.
The proposal would require the Office of Inspector General of HHS (OIG) to report annually,
beginning July 1, 2011, on the extent to which formularies used by prescription drug plans and
MA-PD plans under Part D include drugs commonly used by full-benefit dual eligible
individuals. OIG would also be required to complete a study by October 1, 2011 that would
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compare covered prescription drug prices paid under the Medicare Part D program to those
negotiated by state Medicaid plans for the top 200 drugs determined by both volume and
expenditures including all rebates and discounts received by the Medicaid and Part D plans. The
report would not disclose information that is deemed proprietary or likely to negatively impact a
Medicaid program or Part D plans’ ability to negotiate drug prices. The CBO score is $0.0 billion
for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

Sec. 3314. Including Costs Incurred By AIDS Drug Assistance Programs And Indian Health
Service In Providing Prescription Drugs Toward The Annual Out Of Pocket Threshold
Under Part D.
Under a standard Medicare Part D plan design, beneficiaries must incur a certain
level of out-of-pocket costs ($4,350 in 2009) before catastrophic protection begins. These include
costs that are incurred for the deductible, cost-sharing, or benefits not paid because they fall in the
coverage gap. Costs are counted as incurred, and thus treated as true out-of-pocket (TrOOP) costs
only if they are paid by the individual (or by another family member on behalf of the individual),
paid on behalf of a low-income individual under the subsidy provisions, or paid under a State
Pharmaceutical Assistance Program. Additional payments that do not count toward TrOOP
include Part D premiums and coverage by other insurance, including group health plans, workers’
compensation, Part D plans’ supplemental or enhanced benefits, or other third parties. This
provision would allow costs paid by the Indian Health Service or under an AIDS Drug Assistance
Program to count toward the out-of-pocket threshold for costs incurred on or after January 1,
2011. The CBO score is +$0.2 billion for FY2010-FY2014 and +$0.6 billion for FY2010-FY2019.
Sec. 3315. Immediate Reduction in Coverage Gap in 2010. Medicare law sets out a defined
standard benefit structure under the Part D prescription drug benefit that includes a gap in
coverage (the doughnut hole). In 2009, the standard benefit includes a $295 deductible and a 25%
coinsurance until the enrollee reaches $2,700 in total covered drug spending. After this initial
coverage limit is reached, the enrollee is responsible for the full cost of the drugs until total costs
hit the catastrophic threshold, $6,153.75 in 2009. This provision would increase the previously
announced 2010 standard initial coverage limit of $2,830 by $500,27 thus decreasing the time that
a Part D enrollee would need to be in the coverage gap. There would be no change in the
premiums, bids, or any other parameters as a result of this increase. Additionally, the Secretary
would be required to establish procedures to reimburse drug plan sponsors for the associated
reduction in beneficiary cost sharing. The Secretary would also be required to develop an
estimate of the additional increased costs for increased drug utilization and financing and
administrative costs, and use such estimates to adjust payments to Part D sponsors. The initial
coverage limit would only apply to 2010; the initial coverage limit for plan years beginning in
2011 would be determined as if this 2010 increase had not occurred. The CBO score (combined
with Sec. 3301) is +$7.4 billion for FY2010-FY2014 and +$19.5 billion for FY2010-FY2019.

Subtitle E—Ensuring Medicare Sustainability
Sec. 3401. Revision of Certain Market Basket Updates and Incorporation of Productivity
Improvements into Market Basket Updates That Do Not Already Incorporate Such
Improvements
. Currently, most fee-for-service Medicare providers receive predetermined

27 See CMS fact sheet, CMS Announces 2010 Payment Information for Part C Medicare Advantage Plans and Part D
Prescription Drug Plans, April 6, 2009, http://www.cms.hhs.gov/apps/media/press/factsheet.asp?Counter=3437&
intNumPerPage=10&checkDate=&checkKey=&srchType=1&numDays=3500&srchOpt=0&srchData=&
keywordType=All&chkNewsType=6&intPage=&showAll=&pYear=&year=&desc=false&cboOrder=date
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payment amounts established under different, unique prospective payment systems. Each year,
the base payment amounts in the different Medicare payment systems are increased by an update
factor to reflect the increase in the unit costs associated with providing health care services.
Generally, Medicare’s annual updates are linked to either: (1) projected changes in specific
market basket (MB) indices which are designed to measure the change in the price of goods and
services (such as labor and equipment) that are purchased by the provider and intended to reflect
the effect of inflation on providers’ costs per service; or (2) the Consumer Price Index for All
Urban Consumers (CPI-U). Generally, the provision would provide for updates based on the MB
or CPI minus full productivity estimates for all Parts A and B providers and suppliers who are
subject to a MB or CPI update. The productivity offset would equal the percentage change in the
10-year moving average of annual economy-wide private nonfarm business multi-factor
productivity. The estimate used would be that published before the promulgation of the regulation
establishing increases in the Medicare rates for the year or period.
Specifically, this change would implement a full productivity adjustment for inpatient and
outpatient hospital services, inpatient psychiatric facilities, inpatient rehabilitation, long term care
hospital services and nursing homes beginning in FY2012. It would implement a full productivity
adjustment for hospice providers beginning in FY2013. In addition, it would implement a full
productivity adjustment for home health providers beginning in FY2015. For providers paid
through the clinical laboratory test fee schedule, the proposal would replace the scheduled 0.5%
payment reduction for calendar years 2011 through 2013 with a full productivity adjustment for
calendar year (CY) 2011 and subsequent years. All other productivity adjustments for other Part
B providers would begin in CY2011. Except where noted below, the application of the update
adjustments would be able to result in a negative factor and a basis of payment that would be
lower than in the preceding year. The update factors for Medicare providers and suppliers would
be subject to the following adjustments:
Acute care hospitals, long term care hospitals, inpatient rehabilitation facilities, inpatient
psychiatric facilities, and outpatient hospitals:
Aside from the productivity factor beginning in
FY2012, the MB update for inpatient acute hospitals services would be reduced 0.25 percentage
points in FY2010 and FY2011. In FY2012 and FY2013, the MB update would be reduced 0.2
percentage points. For each of the fiscal years from FY2014 through FY2019, the 0.2 percentage
point reduction to the MB would be contingent upon the level of the insured nonelderly
population relative to the projection of insured population for the year preceding enactment
(CBO’s fiscal year estimate at time of enrollment of the bill in either House). Specifically, only if
the level of non-elderly insured population is 5 or fewer percentage points above the projections,
would the MB update be reduced by 0.2 percentage points. Skilled nursing facilities: The SNF
MB update would be subject to the productivity factor adjustment beginning in FY2012. Home
health agencies:
Aside from the productivity factor adjustment beginning in 2015, the MB
update for home health services would be reduced by 1.0 percentage point in 2011 and 2012.
Hospice care: The hospice MB update would be subject to the productivity factor adjustment
beginning in FY2013. Aside from the productivity factor adjustment, the MB update would be
reduced by 0.5 percentage points in FY2013. For each of the fiscal years from FY2014 through
FY2019, a 0.5 percentage point reduction to the MB would be contingent upon the level of the
insured population relative to the projection of insured population the year preceding enactment.
Dialysis: The ESRD MB would no longer be subject to a 1 percentage point reduction beginning
in 2012, but would be subject to the productivity factor adjustments starting in 2012. Ambulance
services:
The productivity adjustment factor would be applied to the CPI-U used to increase the
ambulance fee schedule starting in CY2011. Ambulatory surgical services: The productivity
adjustment factor would be applied to the CPI-U used to update payments for ambulatory surgical
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services starting in CY2011. Laboratory services: The existing 0.5 percentage point reduction to
the CPI-U update to the fee schedule in CY2009 and CY2010 would be retained. A 1.75
percentage point reduction to the update in CY2011 through CY2015 would be established; this
reduction would be able to result in a negative update. The productivity adjustment factor would
be applied to the CPI-U starting in CY2011, but in the application of the adjustment would not be
able to reduce the increase to less than zero. Certain durable medical equipment: The
productivity adjustment factor would be applied to the CPI-U used to increase the fee schedules
for certain durable medical equipment (DME) beginning in CY2011. Certain DME would have
received a payment increase of CPI-U plus 2 percentage points in CY2014. The 2 percentage
point increase was eliminated. Prosthetic devices, orthotics, and prosthetics: The productivity
adjustment factor would be applied to the CPI-U update for the applicable fee schedule for this
DME category starting in CY2011. Other items: The productivity adjustment factor would be
applied to the CPI-U update for this DME category starting in CY2011. The CBO score is -$24.4
billion for FY2010-FY2014 and -$150.0 billion for FY2010-FY2019.

Sec. 3402. Temporary Adjustment to the Calculation of Part B Premiums. Medicare Part B
finances coverage for physicians’ and other outpatient services, in part through premiums paid by
beneficiaries who enroll in the voluntary program. Before January 2007, the Part B premium was
set at 25 percent of the program’s costs per aged enrollee (enrollees who were age 65 or older)
and was applied universally to all enrollees. Since then, under a provision of the Medicare
Modernization Act, approximately 1.7 million higher-income beneficiaries have faced
progressively greater shares of those costs—35 percent, 50 percent, 65 percent, or 80 percent,
depending on income. The income categories that those shares apply to are based on enrollees’
modified adjusted gross income. In 2009, the income thresholds for those premium shares are
$85,000, $107,000, $160,000, and $213,000, respectively. (For married couples, the
corresponding income thresholds are twice those values.) The income thresholds rise each year
with changes in the consumer price index. The provision would freeze the current income
thresholds for the period of 2011 through 2019 at the 2010 levels. The CBO score is -$7.5 billion
for FY2010-FY2014 and is- $25.0 billion for FY2010-FY2019.

Sec. 3403. Independent Medicare Advisory Board. This provision would establish an
Independent Medicare Advisory Board to develop and submit detailed proposals to Congress and
the President to reduce Medicare spending. The Board would consist of 15 members with
expertise in health care financing, delivery, and organization. All members would be appointed by
the President and confirmed by the Senate. Proposals would primarily focus on payments to MA
and PDP plans and reimbursement rates for certain providers. The Board would be prohibited
from developing proposals related to Medicare benefits, eligibility, or financing. Proposals, which
would only be required in certain years, would have to meet specific savings targets.
Recommendations made by the Board would automatically go into effect unless Congress
enacted specific legislation to prevent their implementation. The first year the Board’s proposals
could take effect would be 2015.
Membership and Structure. The Board would be composed of 15 members, appointed by the
President with the advice and consent of the Senate. Members of the Board would serve six-year,
staggered terms. Members could not serve more than 2 full consecutive terms. The Senate
Majority Leader, the Speaker of the House, the Senate Minority Leader, and the House Minority
Leader would each present three recommendations for appointees to the President. The President,
with the advice and consent of the Senate, would also be required to appoint a Chair for the
Board. The Board would elect a Vice Chairman. Members could only be removed by the
President for neglect of duty or malfeasance in office. In addition to the 15 members of the
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Board, the Secretary of Health and Human Services (HHS), the Administrator of the Center for
Medicare and Medicaid Services (CMS), and the Administrator of the Health Resources and
Services Administration (HRSA) would serve as ex-officio, non-voting members of the Board.
Qualifications for membership would be similar to the qualifications required for members of the
Medicare Payment Advisory Board (MedPAC). Individuals involved in the delivery or
management of health care services could not constitute a majority of the Board. In addition to
these qualifications, the President would be required to establish a system for publicly disclosing
any financial or other conflicts of interests relating to members. Individuals that engage in any
other business, vocation, or employment could not serve as appointed members of the Board.
Members would be considered officers in the executive branch for purposes of applying Title I of
the Ethics in Government Act of 1978. After serving on the Board, former members would be
barred from lobbying the Board and other relevant executive branch departments and agencies
and relevant congressional committees for one year.
The Chair would be responsible for exercising all of the Board’s executive and administrative
functions, including those related to the appointment and supervision of employees and the use of
funds. All requests for discretionary appropriations to fund the Board’s activities must be
approved by a majority vote.
Requirements for Proposal Submission. The provision would require that the Board submit
proposals to the President for years in which the projected rate of growth in Medicare spending
per beneficiary exceeds a target growth rate. Determinations of the projected and target growth
rates would be made by the CMS Office of the Actuary (OACT) beginning in 2013.28 The Board
would be required to submit its first proposal to the President by January 15th, 2014 for
implementation in 2015.
For years 2014 through 2017, the Board would be required to submit proposals for years in which
the projected rate of growth in Medicare spending per beneficiary exceeds the average of the
projected percentage increase in the Consumer Price Index for All Urban Consumers (CPI) and
the Consumer Price Index for Medical care (CPI-M). Beginning in 2018, proposals would only be
required for years in which the projected rate of growth in Medicare spending exceeds the
average of the CPI, the CPI-M, and the Gross Domestic Product (GDP) plus 1.0%. The Board
would not be required to submit a proposal to the President after 2018 if the OACT determines
that the projected rate of growth in National Health Expenditures (NHE) exceeded the projected
rate of growth in Medicare spending. Recommendations proposed by the Board would be
required to reduce Medicare spending by the lesser of 0.5 percentage points in 2015, 1.0
percentage points in 2016, 1.25 percentage points in 2017, 1.5 percentage points in 2018 and the
amount by which the rate of growth in Medicare spending exceeds the target growth rate.
Proposals could not increase Medicare spending over a 10-year period.
Scope of Proposals. The Senate Amendment lays out a number of specific fiscal and policy
criteria which the Board would be required to meet in making its recommendations. When
developing and submitting proposals, the Board would be required, to the extent feasible, to: (1)
prioritize recommendations that would extend Medicare solvency and target reductions to sources

28 The projected Medicare growth rate per beneficiary would be calculated as a projected five-year average of the
growth in Medicare spending. Projections would be required to assume a zero update in payments for physicians. The
projection would also be required to take into account any delivery system reforms or payment changes that have not
yet been implemented.
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of excess cost growth; (2) include only those recommendations that improve the health care
delivery system, including the promotion of integrated care, care coordination, prevention and
wellness and quality improvement and protect beneficiary access to care, including in rural and
frontier areas; (3) consider the effects of changes in provider and supplier payments on
beneficiaries; consider the effects of proposals on any provider who has, or is projected to have,
negative profit margins or payment updates; 4) consider the unique needs of individuals dually
eligible for Medicare and Medicaid, and 5) include recommendations for administrative funding
to carry out its recommendations.
As appropriate, each proposal would be required to include recommendations that would reduce
spending in Medicare Parts C and D. Reductions could be obtained by reducing Medicare
payments for administrative expenses to MA and PDP plans, denying or removing high bids for
drug coverage from the calculation of the monthly bid amount for Part D plans, and reducing
performance bonuses for MA plans. Recommendations could not target the base beneficiary
premium percentage for Part D plans.
The Board would be prohibited from making recommendations that would ration care, raise
revenues, increase beneficiary premiums, increase beneficiary cost-sharing, restrict benefits, or
modify eligibility. Additionally, proposals submitted before December 2018 for implementation
in 2020, could not include recommendations that would reduce payments to providers and
suppliers scheduled to receive a reduction in their payment updates in excess of a reduction due to
productivity.
Presidential Review. At the beginning of the year following the determination by the Secretary,
the Advisory Board is to submit its recommendations to the President who is to, in turn,
immediately submit them to Congress. The Senate Amendment dictates certain information which
must accompany the Advisory Board’s submission, including a requirement for legislative
language implementing the recommendations.
Congressional Consideration. Section 3403 directs the Secretary to automatically implement the
Board’s recommendations unless Congress, by August 15 of the year in which the
recommendations are submitted, enacts legislation superseding the Board’s proposal. The Senate
Amendment establishes special “fast track,” parliamentary procedures governing congressional
consideration of legislation implementing the Board’s recommendations. These fast track
procedures differ from the normal parliamentary mechanisms used by the chambers to consider
most legislation and are designed to ensure that Congress, should it choose to do so, can act
quickly on the proposal put forth by the Advisory Board.
The fast track procedures established by the Senate Amendment mandate the introduction of the
Board’s legislative proposal by the House and Senate majority leaders “by request” on the day it
is submitted to Congress. When introduced, such legislation is to be referred to the Senate
Committee on Finance and to the House Committees on Energy and Commerce and Ways and
Means. These committees may mark up the measure, and must report it to their respective
chambers not later than April 1 or be discharged of its further consideration. The expedited
procedure established by the Senate’s amendment waives the provisions of Senate Rule XV
which would ordinarily bar the Finance Committee from reporting a committee amendment
containing significant matter not in its jurisdiction so long as the amendment in question “is
relevant” to a proposal in the Advisory Board bill.
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The Senate Amendment includes provisions which are intended to restrict the House or Senate
from considering any amendment (including committee amendment), bill, or conference report
which would repeal or change the Board’s recommendations unless those changes meet the same
fiscal and policy criteria (described above) which the Board was required to meet in developing
its recommendations. The authors of the Senate Amendment provide for this restriction to apply
not only to House and Senate consideration of the Board legislation submitted by the President,
but to all other legislation Congress considers as well. This restriction may be waived solely by a
vote of three-fifths of the Members duly chosen and sworn, and in addition, the substitute
prohibits the consideration of legislation that would repeal or modify this restriction.29
No expedited procedures are established for initial House floor consideration of the Board’s
legislation. The House would presumably establish the terms of its consideration of the legislation
by adopting a special rule reported by the House Committee on Rules. In the Senate, a motion to
proceed to consider the legislation is privileged and not debatable. Amendments offered to the
legislation on the Senate floor must be germane and may not reduce the savings in Medicare per
capita growth below established targets. Debate in the Senate on each amendment to the bill is
limited and overall Senate consideration of the legislation may not exceed 30 hours, after which a
final vote will be taken on it.
The Senate Amendment also includes “fast track” provisions which are intended to facilitate the
exchange of legislation between the House and Senate by establishing an automatic “hookup” of
the versions passed by the two chambers. In the event that there is a need to resolve bicameral
differences on the legislation, debate on any conference report or amendment exchange is limited
to no more than 10 hours, after which a final vote will occur. Should the measure be vetoed,
Senate debate on a veto message is limited to one hour.
Fast Track Consideration of Legislation to Discontinue Medicare Advisory Board. The
Senate Amendment establishes an additional set of fast track parliamentary procedures governing
House and Senate consideration of a joint resolution to discontinue the Independent Medicare
Advisory Board and the “automatic” process of implementation described above. These
procedures ensure that the House and Senate may act promptly on such a measure by limiting
debate and amendment at the committee and floor level. The procedures also establish a
supermajority requirement of three-fifths of Members duly chosen and sworn for passage of such
a joint resolution in each chamber.30
Additional Review Procedures. The Board must submit a draft copy of each proposal it develops
to the Medicare Payment Advisory Commission (MedPAC) and to the Secretary for review.
Funding. The provision would appropriate $15 million to the Board to carry out its functions
beginning in year 2012. This amount would increase by the rate of inflation for each year
thereafter. Sixty percent of the appropriation would come from the Part A Medicare Trust Fund
and 40 percent from the Part B Trust Fund.

29 It is not clear, and will likely require further clarification by the House and Senate, in close consultation with the
Parliamentarians of the respective chambers, how these provisions, which attempt to limit congressional consideration
of any other legislation changing or differing from an Advisory Board recommendation, could be enforced in practice.
30 If such a joint resolution were vetoed, as one might argue could be likely, it would require a two-third’s vote of each
chamber to override and enact the measure.
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Oversight Mechanisms. The provision would establish a consumer advisory council to advise the
Board on the impact of payment policies on consumers. The Council would be composed of 10
consumer representatives appointed by the Comptroller General of the United States, each from
among the 10 regions established by the Secretary. The provision would also require the GAO to
conduct a study on changes in payment policies, methodologies, rates, and coverage policies
under Medicare resulting from the Board’s proposal. Specifically, the study would provide an
assessment of the effect of the Board’s proposal on Medicare beneficiary’s access to providers,
affordability of premiums and cost-sharing, the potential impact of changes on other government
or private sector purchasers of care, and the quality of care provided. The report would be due by
July 1, 2015. The GAO would conduct additional studies as appropriate.
The CBO score is $0 for FY2010-FY2014 and -$23.4 billion for FY2010-FY2019.31
Senate Amendment 2826 (Agreed to December 3, 2009)
Sec. 3601. Protecting and Improving Guaranteed Medicare Benefits. This section would
require that that no provisions in the Senate Amendment could result in a reduction in Medicare
benefits currently guaranteed under Title XVIII. Amendment 2826 also would require that
Medicare savings achieved under the Senate Amendment in the nature of a substitute to H.R.
3590 are to be used to extend the solvency of the Medicare trust funds, reduce Medicare
premiums and other cost-sharing for beneficiaries, improve or expand guaranteed Medicare
benefits, and protect access to Medicare providers.
Title IV—Prevention of Chronic Disease and Improving Public
Health

Subtitle B—Increasing Access to Clinical Prevention Services.32
Sec. 4103. Medicare Coverage of Annual Wellness Visit Providing a Personalized Prevention
Plan.
Medicare covers a one-time initial preventive physical examination (IPPE), for purposes of
health promotion and disease detection, which includes education, counseling, and referrals with
respect to screening and other preventive services. The IPPE is reimbursable only if provided
within one year of Medicare Part B enrollment. Medicare does not otherwise cover periodic
routine health examinations (i.e., those provided in the absence of symptoms).
The U.S. Preventive Services Task Force (USPSTF), administered by the HHS Agency for
Healthcare Research and Quality (AHRQ), is an independent panel of private-sector experts in
primary care and prevention that conducts assessments of scientific evidence of the effectiveness
of a broad range of clinical preventive services, including screening, counseling, and preventive
medications.33 It provides evidence-based recommendations for the use of preventive services,
which may vary depending on age, gender, and risk factors for disease, among other

31 Subtitle F on health care quality improvements is discussed in CRS Report R40943, Public Health, Workforce,
Quality, and Related Provisions in the Senate Amendment in the Nature of a Substitute to H.R. 3590
.
32 All other provisions in Title IV are addressed in CRS Report R40943, Public Health, Workforce, Quality, and
Related Provisions in the Senate Amendment in the Nature of a Substitute to H.R. 3590
.
33 See the U.S. Preventive Services Task Force, http://www.ahrq.gov/clinic/uspstfix.htm.
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considerations. Services are given a grade of A, B, C, D or an I Statement. Services graded A or B
are recommended. For services graded C, the USPSTF makes no recommendation for or against
their routine use. For services graded D, the USPSTF recommends against routinely providing the
service to asymptomatic patients, based on evidence that the service is not beneficial, and may be
harmful. “I” Statements are provided when evidence is insufficient to support a recommendation.
Under this provision, Medicare Part B would cover, beginning in 2011, personalized prevention
plan services, including a comprehensive health risk assessment. The personalized plan could
include several specified elements, among them: review and update of medical and family
history; a 5- to 10-year screening schedule and referral for services recommended by the USPSTF
and ACIP; a list of identified risk factors and conditions, and a strategy to address them; lists of
all medications currently prescribed and all providers regularly involved in the patient’s care;
review or referral for testing and treatment of chronic conditions; and cognitive impairment
assessment. All enrolled beneficiaries would be eligible for personalized prevention plan services
once every year, without any cost sharing. During the first year of Part B enrollment,
beneficiaries could choose to receive either the IPPE or personalized prevention plan services, but
not both. The Secretary would be required to develop appropriate guidance, and conduct outreach
and related activities, with respect to personalized prevention plan services and health risk
assessments. The CBO score is $1.6 billion for FY2010-FY2014 and $3.7 billion for FY2010-
FY2019.

Sec. 4104. Removal of Barriers to Preventive Services in Medicare. Section 1833(a) of the
SSA establishes coinsurance for the beneficiary, generally requiring Medicare to cover 80% of the
costs of covered services under Part B, with specified exceptions. Section 1833(b) establishes an
annual deductible for which the beneficiary is responsible. These sections have been amended
over the years to waive coinsurance and/or the deductible for many, but not all, covered
preventive services.
The provision would amend SSA Sec. 1861 to define preventive services covered by Medicare to
mean a specified list of currently covered services, including colorectal cancer screening services
even if diagnostic or treatment services were furnished in connection with the screening. The list
would also include the IPPE, as well as the personalized prevention plan services that would be
covered pursuant to Sec. 4103 of this amendment. Coverage would continue to be subject to all
criteria that apply to each preventive service covered under current law. The provision would also
amend SSA Sec. 1833 to waive beneficiary coinsurance requirements for most preventive
services, requiring Medicare to cover 100% of the costs. Services for which no coinsurance
would be required are the IPPE, personalized prevention plan services, any additional preventive
service covered under the Secretary’s administrative authority, and any currently covered
preventive service (including medical nutrition therapy, and excluding electrocardiograms) if it is
recommended with a grade of A or B by the USPSTF. The provision would generally waive the
application of the deductible for the same types of preventive services noted above for which
coinsurance would be waived. It would not, however, waive the application of the deductible for
any additional preventive service covered under the Secretary’s administrative authority. The
CBO score is $0.3 billion for FY2010-FY2014 and $0.8 billion for FY2010-FY2019.

Sec. 4105. Evidence-Based Coverage of Medicare Preventive Services. The provision would
authorize the Secretary to modify the coverage of any currently covered preventive service
(including services included in the IPPE, but not the IPPE itself), to the extent that the
modification is consistent with USPSTF recommendations. The provision would also allow the
Secretary to withhold payment for any currently covered preventive service graded D (i.e., not
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recommended) by the USPSTF. The enhanced authority and the prohibition would not apply to
services furnished for the purposes of diagnosis or treatment (rather than as preventive services
furnished to asymptomatic patients). The CBO score is -$0.3 billion for FY2010-FY2014 and
-$0.7 billion for FY2010-FY2019.

Subtitle C—Creating Healthier Communities.
Sec. 4202. Medicare Demonstration: Promotion of Healthy Lifestyles. Subsection (b) of this
provision would require the Secretary to conduct an evaluation of community-based prevention
and wellness programs, and based on findings, develop a plan for promoting healthy lifestyles
and chronic disease self-management for Medicare beneficiaries. The evaluation would include
an evidence review of literature, best practices, and resources, and an evaluation of existing
community prevention and wellness programs sponsored by the Administration on Aging. To
fund the evaluation, the Secretary would be required to transfer to CMS $50 million in total from
the Part A and Part B Trust Funds, in whatever proportion the Secretary determines. Activities
under this evaluation would not be subject to review under the Paperwork Reduction Act of 1995,
which subjects collections of information from the public to clearance by OMB. The CBO score
is $0.1 billion for FY2010-FY2014 and $0.1 billion for FY2010-FY2019.

Sec. 4204. Immunizations. Among other requirements, this section would require a GAO study
and report to Congress on the impact of the coverage of vaccines under Medicare Part D on
access to those vaccines by beneficiaries who are 65 years of age or older. The section would
appropriate $1 million for FY2010 for this study. The CBO score is between -$50 million and
+$50 million for FY2010-FY2014 and for FY2010-FY2019.

Title V—Health Care Workforce
Subtitle F—Strengthening Primary Care and Other Workforce Improvements34
Sec. 5501. Expanding Access to Primary Care Services and General Surgery Services.
Medicare uses a fee schedule to reimburse physicians for the services they provide. In certain
circumstances, physicians receive an additional payment to encourage targeted activities. These
bonuses, typically a percentage increase above the Medicare fee schedule amounts, can be
awarded for a number of activities including demonstrating quality achievements, participating in
electronic prescribing, or practicing in underserved areas. For instance, Section 1833(m) of the
Social Security Act provides bonus payments for physicians who furnish medical care services in
geographic areas that are designated by the Health Resources and Services Administration
(HRSA) as primary medical care health professional shortage areas (HPSAs) under section 332
(a)(1)(A) of the Public Health Service (PHS) Act. The bonus payment equals 10% of what would
otherwise be paid under the fee schedule.
The provision would establish a new 10% bonus on select evaluation & management and general
surgery codes under the Medicare fee schedule for five years, beginning January 1, 2011. The
primary care service codes to which this bonus would apply would be office visits, nursing

34 All other Title V provisions are discussed in Those provisions are discussed in CRS Report R40943, Public Health,
Workforce, Quality, and Related Provisions in the Senate Amendment in the Nature of a Substitute to H.R. 3590
.

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facility visits, and home visits. The bonus would be available to primary care practitioners who
(1) are physicians who have a specialty designation of family medicine, internal medicine,
geriatric medicine, or pediatric medicine, or are nurse practitioners, clinical nurse specialists, or
physician assistants, and (2) furnish 60% of their services in the select codes.
Practitioners providing major surgical procedures in health professional shortage areas would also
be eligible for a bonus under this provision. Over the same five year period beginning January 1,
2011, general surgeons providing care in a HPSA would also be eligible for a 10% bonus on
major surgical procedure codes, defined as surgical procedures for which a 10-day or 90-day
global period is used for payment under the Medicare fee schedule.
The review and adjustment of RVUs (under Section 1848(c)(2)(B)) would be adjusted for these
incentives; only half (50%) of the cost of the bonuses would be taken into consideration in the
budget neutrality calculation in 2011 and in subsequent years, with an across-the-board reduction
to all codes (through a modification of the conversion factor) accounting for the adjustment,
except for physicians who primarily provide services in health professionals shortage areas. The
CBO score is $1.1 billion for FY2010-FY2014 and is $1.6 billion for FY2010-FY2019.

Sec. 5502. Medicare Federally Qualified Health Center Improvements. A federally qualified
health center (FQHC) is a type of provider defined by the Medicare and Medicaid statutes.
FQHCs include all organizations receiving grants under section 330 of the Public Health Service
Act (PHSA), clinics that have been certified as meeting such requirements (called FQHC Look-
Alikes) or outpatient facilities that are operated by tribal organization or urban Indian
organizations. FQHC services are defined by Medicare statute as rural health clinic services (such
as physician services, those provided by physician assistants, nurse practitioners, nurse midwives,
visiting nurses, clinical psychologist or social workers and related services and supplies), diabetes
outpatient self-management training services, medical nutrition therapy services and preventive
primary health services required under section 330 of the Public Health Service Act (PHSA).35
FQHCs receive cost-based reimbursement from Medicare, subject to a per-visit payment limit
and certain productivity standards. Medicare pays FQHCs on an interim basis for covered
services furnished to beneficiaries using an all-inclusive rate for each visit (except for certain
vaccines which are paid on a cost basis). Generally, the FQHC’s final payment rate is calculated
by dividing the FQHC’s total allowable cost for such services by the total visits which is subject
to the maximum per-visit payment limit. The payment limits are increased each year by the
Medicare Economic Index (MEI) and are different for urban and rural FQHCs. The upper
payment limit per visit for urban FQHCs is $119.29 starting January 1, 2009, through December
31, 2009 and per visit limit for rural FQHCs is $102.58 effective January 1, 2009.
Effective for services starting on January 1, 2011, the statutory definition of FQHC services
would include the Medicare definition of preventive services at 1861(ddd)(3) that would be
established in Section 2002 of this legislation. These services would include screening and
preventive services (other than electrocardiograms), an initial preventive physical examination,

35 The preventive services as defined by the PHSA include prenatal and perinatal services; appropriate cancer
screening; well-child services; immunizations against vaccine-preventable diseases; screenings for elevated blood lead
levels, communicable diseases, and cholesterol; pediatric eye, ear, and dental screenings to determine the need for
vision and hearing correction and dental care; voluntary family planning services; preventive dental services.

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and personalized prevention plan services. The cross reference to preventive services in the PHSA
would be retained.
The Secretary would develop a prospective payment system (PPS) for FQHC services; FQHCs
would be required to submit necessary information for the implementation of such a PPS,
including the reporting of services using medical coding conventions. PPS payments for FQHC
services would begin October 1, 2014. The PPS system would be implemented so that the
resulting expenditures are 103% of what would have been spent under the prior system. FQHC
payment rates would be increased by the MEI in each subsequent year. The CBO score is between
-$50 million and +$50 million for FY2010-FY2014 and $0.2 billion for FY2010-FY2019.

Title VI—Transparency and Program Integrity
Subtitle A—Physician Ownership and Other Transparency
Sec. 6001. Limitation on Medicare Exception to the Prohibition on Certain Physician
Referrals for Hospitals.
Physicians are generally prohibited from referring Medicare patients for
certain services to facilities in which they (or their immediate family members) have financial
interests. However, among other exceptions, physicians are not prohibited from referring patients
to whole hospitals in which they have ownership or investment interests. Providers that furnish
substantially all of their designated health services to individuals residing in rural areas are
exempt as well. Under this provision, beginning no later than 18 months after the date of
enactment, only physician-owned hospitals meeting certain requirements would be exempt from
the prohibition on self-referral. Hospitals that have physician ownership and a provider agreement
in operation on February 10, 2010, and that met other specified requirements would be exempt
from this self-referral ban. These requirements include a limitation on the expansion of the
facilities’ service capacity and would address conflicts of interest, bona fide investments, and
patient safety issues. In addition, the hospital could not have converted from an ambulatory
surgical center to a hospital after the date of enactment.
Exempt hospitals meeting those requirements would not be permitted to increase the number of
operating rooms, procedure rooms or beds for which the hospital is licensed as the date of
enactment. A process would be established to allow certain hospitals to expand by August 1, 2011
as established by regulations published by July 1, 2011. Hospitals could apply for such an
expansion once every two years. The increase would be limited to facilities on the main campus
of the hospital. There would be no administrative or judicial review of this process. The Secretary
would be required to establish policies and procedures to ensure compliance with these
requirements, beginning on their effective date, including unannounced site reviews of hospitals.
These audits would begin no later than November 1, 2011. The CBO score is -$0.2 billion for
FY2010-FY2014 and -$0.7 billion for FY2010-FY2019.

Sec. 6002. Transparency Reports and Reporting of Physician Ownership or Investment
Interests.
This provision would add a new section 1128G to the Social Security Act to require
covered drug, device, biological, or medical supply manufacturers that make a payment or
another transfer of value to a physician (other than employees of a manufacturer) or a teaching
hospital to report annually, in electronic form, specified information on such transactions to the
Secretary of HHS. Certain information would be excluded from these reporting requirements,
including payments or transfers of $10 or less, unless the aggregate annual payments or transfers
to a recipient exceeds $100 (which, after 2012, would be indexed for inflation), samples intended
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for patient use, patient educational materials, and loans of a covered device for a short-term time
period. The provision would also require manufacturers, or group purchasing organizations to
report annually to the Secretary, in electronic form, certain information regarding an ownership or
investment interest held by a physician (or an immediate family member) in the manufacturer or
group purchasing organization during the preceding year. Certain penalties would apply for
failure to submit these reports to the Secretary. The Secretary would also be required to establish
procedures to ensure public availability of the information to be submitted under this section. The
CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

Sec. 6003. Disclosure Requirements for In-Office Ancillary Services Exception to the
Prohibition on Physician Self-Referral for Certain Imaging Services.
This section would
amend section 1877 of the Social Security Act, which prohibits physician referrals, for certain
services that may be paid for by Medicare, to entities with which the physician has a financial
relationship. Specifically, section 6003 would amend one of the exceptions to this prohibition, the
in-office ancillary services exception. The provision would add a requirement that with respect to
magnetic resonance imaging, computed tomography, positron emission tomography, and any
other designated health services as determined by the Secretary, the referring physician must
inform the individual in writing at the time of the referral that the individual may obtain the
services from a person other than the referring physician, a physician who is a member of the
same group practice as the referring physician, or an individual who is directly supervised by the
physician or by another physician in the group practice. The individual must be provided with a
written list of suppliers who furnish these services in the area in which the individual resides. The
CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

Sec. 6004. Prescription Drug Sample Transparency. The bill would add a new section 1128H
of the Social Security Act to require drug manufacturers and authorized distributors of an
applicable drug to submit annually to the Secretary of Department of Health and Human Services
the identity and quantity of drug samples requested and distributed under section 503 of the
Prescription Drug Marketing Act of 1987 (PDMA, P.L. 100-293). This submission must be
aggregated by the name, address, professional designation, and signature or the practitioner
making the request for the sample (or an individual acting on the practitioner’s behalf), as well as
any other category of information that the Secretary determines is appropriate. An applicable drug
is defined to include drugs that are available by prescription and for which payment is available
under Medicare or a Medicaid state plan (or a waiver of such plan). The CBO score is $0.0 billion
for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

Sec. 6005. Pharmacy Benefit Managers Transparency Requirements. Pharmacy benefit
managers (PBMs) are companies that administer drug benefit programs for employers and health
insurance carriers. Drug manufacturers may provide “rebates” to PBMs for a particular drug in
exchange for the placement of the drug on the PBM’s formulary (it’s list of approved drugs). The
proposal would require PBMs that manage prescription drug coverage under a contract with a
Part D drug plan or a qualified health benefits plan offered through an exchange, established by a
state under Section 1311 of this proposed amendment, to share certain financial information with
the Secretary of HHS, the plans the PBMs contract with through Medicare Part D, or the
exchanges in a manner, form, and timeframe specified by the Secretary. Specifically, PBMs
would be required to disclose information on: (1) the percent of all prescriptions that are provided
through retail pharmacies compared to mail order pharmacies, and the generic dispensing rates
for each type of pharmacy (for example, independent, chain, supermarket or mass merchandiser
pharmacy) that is paid by the PBM under contract; (2) the aggregate amount and types of rebates,
discounts or price concessions that the PBM negotiates on behalf of the plan and the aggregate
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amount of these that are passed through to the plan sponsor, and the total number of prescriptions
dispensed; and (3) the aggregate amount of the difference between the amount the plan pays the
PBM and the amount that the PBM pays the retail and mail order pharmacy, and the total number
of prescriptions dispensed. This information would be considered confidential and would be
protected by the Secretary. The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion for
FY2010-FY2019.36

Subtitle D—Patient-Centered Outcomes Research
Sec. 6301. Patient-Centered Outcomes Research. The need for credible information about
which clinical strategies work best, under what circumstances and for whom has been widely
recognized by clinicians, patients, researchers and policy makers. Commonly referred to as
comparative effectiveness research (CER), the Institute of Medicine (IOM) defines this type of
research as the “the generation and synthesis of evidence that compares the benefits and harms of
alternative methods to prevent, diagnose, treat, monitor a clinical condition and improve delivery
of care” with the aim of tailoring decisions to the needs of individual patients. CBO has referred
to CER as “a comparison of the impact of different options that are available for treating a given
medical condition for a particular set of patients.” MedPAC has referred to “comparative-
effectiveness” as “analysis [that] compares the clinical effectiveness of a service (drugs, devices,
diagnostic and surgical procedures, diagnostic tests, and medical services) with its alternatives.”
The phrase “patient-centered outcomes research” has also been used as an alternate term.
Most recently, comparative effectiveness research has been addressed in current law by the
Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (MMA, P.L. 108-173)
and the American Recovery and Reinvestment Act of 2009 (ARRA, P.L. 111-5). Section 1013 of
the MMA authorizes the Agency for Healthcare Research and Quality (AHRQ) to conduct and
support research on outcomes, comparative clinical effectiveness, and appropriateness of
pharmaceuticals, devices, and health care services. The section also prohibits the Center for
Medicare and Medicaid Services (CMS) from using the data to withhold coverage of a
prescription drug. The ARRA provided $1.1 billion in funds to support the development and
dissemination of CER. ARRA also asked the Institute of Medicine to recommend national
priorities for the research to be addressed by ARRA funds.
The bill modifies Title XI of the Social Security Act to add a Part D, Comparative Clinical
Effectiveness Research after sections on General Provisions, Peer Review, and Administrative
Simplification. The proposal would authorize the establishment of a private, non-profit, tax-
exempt corporation, which would be neither an agency nor establishment of the United States
government that would be known as the “Patient-Centered Outcomes Research Institute.” This
institute would enhance the capacity to conduct comparative clinical effectiveness research
(CCER). The purpose of the Institute would be to “assist patients, clinicians, purchasers, and
policy makers in making informed health decisions by advancing the quality and relevance of
evidence concerning the manner in which diseases, disorders, and other health conditions can
effectively and appropriately be prevented, diagnosed, treated, monitored, and managed through
research and evidence synthesis that considers variations in patient sub- populations, and the

36 Subtitle B on nursing home transparency and Subtitle C on background checks are discussed in CRS Report R40943,
Public Health, Workforce, Quality, and Related Provisions in the Senate Amendment in the Nature of a Substitute to
H.R. 3590
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dissemination of research findings with respect to the relative health outcomes, clinical
effectiveness, and appropriateness of the medical treatments, services, and items.”
The duties of the Institute would be to (1) identify research priorities and establish a research
agenda, (2) carry out the research project agenda, (3) collect relevant data from CMS and other
sources, (4) appoint expert advisory panels, (5) support patient and consumer representatives, (6)
establish a methodology committee, (7) provide for a peer-review process for primary research,
and (8) release research findings. The Institute would give preference to the Agency for
Healthcare Research and Quality and the National Institutes of Health in the awarding of
contracts to conduct the research, if the organizations are so authorized in their governing
statutes.
The proposal would establish a Board of Governors for the Institute, which would be responsible
for carrying out the duties of the Institute. The Institute’s Board would consist of the Directors of
AHRQ and the NIH (or their designee) as well as 17 members appointed by the Comptroller
General of the United States representing patients and health care consumers, physicians and
providers, private payers, pharmaceutical, device, and diagnostic manufacturers or developers,
representatives of quality improvement or independent health service researchers, and
representatives of the federal government or the states.
The proposal includes a number of limitations on the use of CCER. A rule of construction
specifying that the Institute is not to be permitted to mandate coverage, reimbursement or other
policies for any public or private payer nor to prevent the Secretary from covering the routine
costs of clinical care received by Medicare, Medicaid, or CHIP beneficiaries in the case where the
individual is participating in a clinical trial where the costs would be covered by the program. in
addition, the Secretary could only use evidence and findings from CCER research to make a
Medicare coverage determination if the process is iterative and transparent and includes public
comment and considers the effect on subpopulations. The Secretary would not use CCER
evidence and findings in determining Medicare coverage, reimbursement, or incentive programs
in a manner that would preclude or have the intent to discourage individuals from choosing health
care treatments based on how the individual values the tradeoff between extending the length of
life and the risk of disability. Nor would the Institute be allowed to develop or employ a dollars-
per-quality adjusted life year or similar measure that discounts value of life because of disability
as a threshold to establish what type of care is cost effective or recommended.
The proposal would create a new trust fund, the Patient-Centered Outcomes Research Trust Fund
(the ‘PCORTF’) in the U.S. Treasury to fund the Institute and its activities. Monies would be
directed to this fund from the general fund of the Treasury as well as the Medicare Trust Funds
and from fees imposed on health insurance and self-insured plans. For FY2013, the Secretary
would transfer amounts from the Medicare Federal Hospital Insurance and the Federal
Supplemental Medical Trust Funds to the PCORTF in proportion to total Medicare expenditures
that come from each Fund for a given year. In FY2013, the amount would be equivalent to $1
multiplied by the average number of individuals entitled to benefits under Part A or enrolled
under Part B of Medicare during the year. In FY2014 through FY2019, the amounts would be
equivalent to $2, adjusted for increases in health care spending FY2014, multiplied by the
average number of such individuals for the given year.
In years 2010, 2011, and 2012, $10 million, $50 million, and $150 million would be appropriated
from Treasury to the fund. In addition, beginning in 2013, the PCORTF would also be financed
from fees on insured and self-insured health plans. For fiscal years 2014 through 2019, the
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proposal would require a transfer of $150 million from the Treasury as well as the net revenues
from a fee of $1 in FY2013 and $2 (adjusted for health care spending increases) in FY2014
through FY2019, on each health insurance policy in the United States multiplied by the number
of lives covered under that policy. Insurance policies that primarily provide non-health benefits
would be exempt. This fee would sunset after FY2019 (plan years ending after September 30,
2019). The CBO score is +$0.1 billion for FY2010-FY2014 and is -$0.3 billion for FY2010-
FY2019.

Subtitle E—Medicare, Medicaid, and CHIP Program Integrity Provisions
Sec. 6401. Provider Screening and Other Enrollment Requirements Under Medicare,
Medicaid, and CHIP.
The enrollment process for participating in Medicare, Medicaid, and CHIP
is different across all three federal programs. This provision would require that the Secretary, in
consultation with the OIG, establish similar procedures for screening providers and suppliers
enrolling in the Medicare, Medicaid, and CHIP programs. Procedures would be required to
include a process for screening, enhanced oversight measures, disclosure requirements,
moratoriums on enrollment, and requirements for developing compliance programs. The
Secretary would have six months from the date this legislation is enacted to develop the
procedures, which would apply to both new and current providers. The Secretary would have
three years to implement these requirements. The level of screening would be determined, with
respect to a category of providers or suppliers, by the Secretary according to the risk of fraud. At
a minimum, all providers and suppliers would be subject to licensure checks, including checks
across states. The Secretary would have the authority to impose additional screening measures
such as criminal background checks, fingerprinting, unannounced site visits, database checks, and
periods of enhanced oversight if necessary. To cover the costs of the screening, providers and
suppliers would be subject to fees, with some exceptions. Fees would start at $200 in 2010 for
individual providers (i.e., physicians), and $500 for institutional providers. The fee would
increase by the rate of inflation thereafter. The Secretary would also have the authority to impose
a temporary moratorium on enrolling new providers if necessary.
The proposal would also impose new disclosure requirements on providers and suppliers
enrolling or re-enrolling in Medicare, Medicaid, or CHIP. Applicants would be required to
disclose current or previous affiliations with any provider or supplier that has uncollected debt,
has had their payments suspended, has been excluded from participating in Medicare, Medicaid,
or CHIP, or has had their billing privileges revoked. The Secretary would be authorized to adjust
payments or deny enrollment in these programs if these affiliations pose an undue risk to the
program.
Lastly, the provision would require Medicare, Medicaid, and CHIP providers and suppliers,
within a particular industry or category, to establish a compliance program. The requirements for
the compliance program would be developed by the Secretary and the OIG. The Secretary would
be required to consider the extent to which compliance programs have been adopted by providers
when creating a timeline for implementation. The CBO score is $0.3 billion for FY2010-FY2014
and $0.6 billion for FY2010-FY2019.

Sec. 6402. Enhanced Medicare and Medicaid Program Integrity Provisions
Data Matching. Currently, claims and payment data for Medicare and Medicaid are housed in
multiple databases. CMS is in the process of consolidating information stored in these databases
into an Integrated Data Repository (IDR). According to the agency’s website, the eventual goal of
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the IDR is to support an integrated data warehouse containing data related to Medicare &
Medicaid claims, beneficiaries, providers, and health plans. This provision would require CMS to
include in the IDR claims and payment data from the following programs: Medicare (Parts A, B,
C, and D), Medicaid, CHIP, health-related programs administered by the Departments of Veterans
Affairs (VA) and Defense (DOD), Social Security, and the Indian Health Service (IHS). The
priority would be the integration of Medicare claims and payment data. Data for the remaining
programs would be integrated as appropriate.
Access to Data. Inspectors General have substantial independence and powers to carry out their
mandate to combat waste, fraud, and abuse, including relatively unlimited authority to access all
records and information of an agency. This provision would grant the OIG and the DOJ explicit
access to Medicare, Medicaid, and CHIP payment and claims data (including Medicare Part D
data) for the purposes of conducting law enforcement and oversight activities. The provision
would also grant the OIG the authority to obtain information (i.e., supporting documentation,
medical records, etc.) from any individual that directly or indirectly provides medical services
payable by a Federal health care program.
Beneficiary Participation in Health Care Fraud Scheme. The provision would require the
Secretary to impose penalties against beneficiaries entitled to or enrolled in Medicare, Medicaid,
or CHIP that knowingly participate in a health care fraud offense.
Overpayments. In accordance with CMS instructions, overpayments must be repaid to CMS
within 30 days of receiving a demand letter. If the debt is not paid in full after 30 days, interest is
assessed and CMS reserves the right to collect the overpayment by offset. Under this provision,
individuals would be required to report and return an overpayment within 60 days. Overpayments
reported after this date would be considered an obligation as defined in Title 31 of the USC.
National Provider Identifier. Health care providers often have many different provider numbers,
one for billing each private insurance plan or public health care program. The administrative
simplification provisions of HIPAA required the adoption and use of a standard unique identifier
for health care providers or National Provider Identifier (NPI). All health care providers who are
considered covered entities under HIPAA were required to obtain and submit claims using an NPI
as of May 2007. This provision would require the Secretary to issue a regulation by January 1,
2011 mandating that all Medicare and Medicaid providers include their NPI on all claims and
enrollment applications.
Medicaid Statistical Information System. States are required to operate an automated claims
processing or Medicaid Management Information System (MMIS) to administer their state plans.
MMISs must be capable of providing timely and accurate data, meet other specifications as
required by the Secretary, and provide for electronic transmission of claims data as well as be
consistent with Medicaid Statistical Information Systems data formats. This provision would
provide the Secretary with the authority to withhold the federal matching payment to states for
medical assistance expenditures when the state does not report enrollee encounter data (as defined
by the Secretary) in a timely manner (as determined by the Secretary) to the state’s MMIS.
Permissive Exclusions. HHS OIG has the authority to exclude health care providers from
participation in Federal health care programs. Exclusions are mandatory under certain
circumstances, and permissive in others (i.e., HHS OIG has discretion in whether to exclude an
entity or individual). This provision would subject any individual or entity that makes a false
statement or misrepresentation on an application to enroll or participate in a Federal health care
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program to the OIG’s permissive exclusion authority. The provision would explicitly apply to
MA, PDP, and Medicaid managed care plans as well as their participating providers and
suppliers.
Civil Monetary Penalties. Section 1128A (a) of the SSA authorizes the imposition of CMPs on a
person, organization, agency, or other entity that engages in various types of improper conduct
with respect to federal health care programs. This section generally provides for CMPs of up to
$10,000 for each false claim submitted, $15,000 or $50,000 under other circumstances, and an
assessment of up to three times the amount claimed. This provision would add additional actions
that would be subject to CMPs. Specifically, individuals that have been excluded from a Federal
health care program who order or prescribe an item or service, individuals that make false
statements on enrollment applications, bids, or contracts to participate in a federal health care
program, or persons who know of an overpayment and do not return the overpayment would be
subject to CMPs. Under this provision, those who knowingly make a false statement or
misrepresentation on an enrollment application, bid, or contract to participate in a federal health
care program would be subject to a CMP of $50,000 and an assessment of up to three times the
amount claimed.
Testimonial Subpoena Authority. The testimonial subpoena authority grants the authority to issue
subpoenas and require the attendance and testimony of witnesses and the production of any other
evidence that relates to matters under investigation or in question. Under this provision, the
Secretary would be able to issue subpoenas and require the attendance and testimony of witnesses
and the production of any other evidence that relates to matters under investigation or in question
by the Secretary. The Secretary would also have the ability to delegate this authority to the OIG
and the Administrator of CMS for the purposes of a program exclusion investigation.
Surety Bonds. To be eligible to receive a provider number from CMS and bill Medicare, DME
suppliers are required to provide the Secretary with a surety bond in the amount of $50,000 or
greater. A surety bond issued by a State would satisfy this requirement. The Secretary has the
authority to impose these requirements on other Part A and B providers and suppliers, except
physicians. Home health agencies are required to provide the Secretary with a surety bond equal
to 10% of the aggregate Medicare and Medicaid payments made to the agency for that year or
$50,000, whichever is smaller. A surety bond for a home health agency is effective for 4 years,
with limited exceptions. This provision would give the Secretary the authority to require certain
providers and suppliers to provide surety bonds commensurate with the volume of billing. The
value of the bond, however, could not be less than $50,000. The Secretary would also have the
authority to impose this requirement on other providers and suppliers considered to be at risk by
the Secretary.
Payment Suspensions. CMS and its contractors have the authority to withhold payment in whole
or in part if there is reliable evidence of an overpayment or fraud. CMS regulations stipulate the
procedures CMS and its contractors must follow when deciding to suspend payment. The
Secretary would have the authority to suspend payments to a provider or supplier pending a fraud
investigation, except when there is not good cause.
Health Care Fraud and Abuse Control Account. Medicare program integrity and anti-fraud
activities are funded through the Health Care Fraud and Abuse Control (HCFAC) Account.
HCFAC was established by the Health Insurance Portability and Accountability Act of 1996
(HIPAA), which sought to increase and stabilize Federal funding for health care anti-fraud
activities. The HCFAC account funds the fraud control activities conducted by DOJ, HHS, the
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OIG, and the FBI. Total funding for health care fraud activities for FY2009 amounted to
approximately $1.4 billion. This provision would increase funding for HCFAC by $10 million
each year for years 2011 through 2020. The provision would also permanently apply the CPI
adjustment to HCFAC funding. Funds would be allocated in the same manner as in current law
and would be available until expended.
Medicare and Medicaid Integrity Programs. Under the Medicare Integrity Program (MIP), CMS
contracts with private entities to conduct a variety of activities designed to protect Medicare from
fraud, waste, and abuse. Activities include auditing providers, identifying and recovering
improper payments, educating providers about fraudulent providers, and instituting a Medicare-
Medicaid data matching program. Established by DRA, the Medicaid Integrity Program (MIP) is
modeled after Medicare’s MIP program. Medicaid MIP provides HHS with dedicated resources to
contract with entities to reduce fraud, waste, and abuse, and to add 100 full-time equivalent MIP
staff. This provision would require both Medicare and Medicaid Integrity Program contractors to
provide the Secretary and the OIG with performance statistics, including the number and amount
of overpayments recovered, the number of fraud referrals, and the return on investment for such
activities. The Secretary would also be required to conduct evaluations of eligible entities at least
every 3 years. No later than 6 months after the end of the fiscal year, the Secretary would be
required to submit a report to Congress describing the use and effectiveness of MIP funds.The
CBO score is -$1.3 billion for FY2010-FY2014 and -$3.2 billion for FY2010-FY2019.

Sec. 6403. Elimination of Duplication Between the Healthcare Integrity and Protection Data
Bank (HIPDB) and the National Practitioner Data Bank (NPDB).
The HIPAA of 1996
required the Secretary to develop and maintain a national health care fraud and abuse data
collection program for the reporting of adverse actions taken against health care providers. This
database is called the Healthcare Integrity and Protection Data Bank (HIPDB). Prior to the
HIPDB, Congress established the National Practitioner Data Bank or NPDB with the Health Care
Quality Improvement Act of 1986. The NPDB collects data related to the professional
competence of physicians, dentists, and other health care practitioners. The types of information
included in the NPDB are medical malpractice payments, certain adverse licensure actions,
adverse privilege actions, adverse professional society actions, and exclusions from Medicare and
Medicaid. States are required to have a system for reporting adverse actions to the NPDB. This
provision would require the Secretary to transfer the information collected in the HIPDB to the
NPDB, thereby eliminating the HIPDB. Certain agencies and officials as well as health care
providers that were subject to such adverse actions would have access to this information, at a
reasonable fee established by the Secretary. The provision would also require States to have a
system for reporting information with respect to any final adverse action taken against a health
care provider, supplier, or practitioner. The CBO score is $0.0 billion for FY2010-FY2014 and
$0.0 billion for FY2010-FY2019.

Sec. 6404. Maximum Period of Submission of Medicare Claims Reduced to Not More Than
12 months.
Medicare statute requires that payments only be made if a written request for
payment is filed within three calendar years after the year in which the services were provided.
The Secretary is authorized to reduce this period to no less than one year if it deems it necessary
for the efficient administration of the program. As established by CMS regulations, the time limit
on submitting a claim for payment is the close of the calendar year after the year in which the
services were furnished. This provision would require that beginning January 2010, the maximum
period for submission of Medicare claims be reduced to not more than 12 months. The CBO score
is $0.0 billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

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Sec. 6405. Physicians Who Order Items and Services Required to be Medicare Enrolled
Physicians or Eligible Professionals.
In order to receive payment from Medicare, physicians are
required to certify that specified services (i.e., inpatient psychiatric services, post-hospital
extended care services, and home health services) meet certain conditions. In the case of home
health services, physicians are required to certify that such services were required because the
individual was confined to his home and needs skilled nursing care or physical, speech, or
occupational therapy; a plan for furnishing services to the individual has been established; and
such services were provided under the care of a physician. In the case of DME, the Secretary is
authorized to require, for specified covered items, that payment be made for items and services
only if a physician has communicated to the supplier a written order for the item. This provision
would require physicians who order durable medical equipment or home health services to be a
Medicare eligible professional or enrolled in the Medicare program. The Secretary would have
the authority to extend these requirements to other Medicare items and services, including
covered Part D drugs, to reduce fraud, waste, and abuse. The CBO score is -$0.2 billion for
FY2010-FY2014 and -$0.4 billion for FY2010-FY2019.

Sec. 6406. Requirement for Physicians to Provide Documentation on Referrals to Programs
at High Risk of Waste and Abuse.
OIG has “permissive” authority to exclude an entity or an
individual from a federal health program under numerous circumstances, including failing to
supply documentation related to payment for items and services. Beginning January 1, 2010 the
Secretary would have the authority to disenroll, for no more than one year, a Medicare enrolled
physician or supplier that fails to maintain and provide access to written orders or requests for
payment for DME, certification for home health services, or referrals for other items and services
to the Secretary. The provision would also extend the OIG’s permissive exclusion authority to
include individuals or entities that order, refer, or certify the need for health care services that fail
to provide adequate documentation to the Secretary to verify payment. The CBO score is $0.0
billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

Sec. 6407. Face to Face Encounter with Patient Required Before Physicians May Certify
Eligibility for Home Health Services or Durable Medical Equipment Under Medicare.
Home
health services are covered under Medicare Parts A and B. In order to receive payment from
Medicare, physicians are required to certify and re-certify that specified services (i.e., inpatient
psychiatric services, post-hospital extended care services, and home health services) meet certain
conditions. In the case of home health services, physicians are required to certify that such
services were required because the individual was confined to his home and needs skilled nursing
care or physical, speech, or occupational therapy; a plan for furnishing services to the individual
has been established; and such services were provided under the care of a physician. In the case
of DME, the Secretary is authorized to require, for specified covered items, that payment be made
for items and services only if a physician has communicated to the supplier a written order for the
item. This provision would require that physicians have a face-to-face encounter (including
through telehealth) with the individual prior to issuing a certification or re-certification for home
health services or durable medical equipment. The provision would also apply to physicians
making home health certifications in Medicaid and CHIP. The Secretary would be authorized to
apply the face-to-face encounter requirement to other Medicare items and services based upon a
finding that doing so would reduce the risk of waste, fraud, and abuse. The CBO score is -$0.5
billion for FY2010-FY2014 and -$1.3 billion for FY2010-FY2019.

Sec. 6408. Enhanced penalties. Section 1128A (a) of the SSA authorizes the imposition of CMPs
on a person, organization, agency, or other entity that engages in various types of improper
conduct with respect to federal health care programs. This section generally provides for CMPs of
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up to $10,000 for each false claim submitted, $15,000 or $50,000 under other circumstances, and
an assessment of up to three times the amount claimed. This provision would mandate that
persons who knowingly make, use, or cause to be made or used any false statement material to a
fraudulent claim be subject to a civil monetary penalty of $50,000 for each violation. This
provision would also add a new clause to the CMP statute, persons who fail to grant timely
access, upon reasonable request (as defined by the Secretary in regulations), to the Office of the
Inspector General (OIG), for the purpose of audits, investigations, evaluations, or other statutory
functions of the OIG, be subject to CMPs of $15,000 for each day of failure.
Medicare Advantage and Part D Plans. MA plans enter into contracts with the Secretary to
participate in the Medicare program. The Secretary has the authority to impose sanctions and
CMPs on MA plans that violate the terms of the contract. Among the types of violations are
failing to provide medically necessary care, imposing excess beneficiary premiums, expelling or
refusing to re-enroll beneficiaries, and misrepresenting or falsifying information. This provision
would increase the number of violations subject to sanctions and CMPs by the Secretary. Under
the provision, plans that enroll individuals in a MA or Part D plan without their consent (except
Part D dual eligibles), transfer an individual from one plan to another for the purpose of earning a
commission, fail to comply with marketing requirements, including CMS guidance, or employ or
contract with an individual or entity that commits a violation would be subject to sanctions
imposed by the Secretary. This provision would also enhance penalties for MA and Part D plans
that misrepresent or falsify. The CBO score is $0.0 billion for FY2010-FY2014 and $0.0 billion
for FY2010-FY2019.

Sec. 6409. Medicare self-referral disclosure protocol. In 1998, the HHS Office of the Inspector
General (HHS OIG) issued a Self-Disclosure Protocol (SDP), which includes a process under
which a health care provider can voluntarily self-disclose evidence of potential fraud, in an effort,
to avoid the costs or disruptions that may be associated with an investigation or litigation. On
March 24, 2009, HHS OIG issued an “Open Letter to Health Care Providers” that makes
refinements to the SDP. In the Open Letter, HHS OIG announced that it would no longer accept
disclosure of a matter that involves only liability under the physician self-referral law in “the
absence of a colorable anti-kickback statute violation.” Further, for anti-kickback-related
submissions accepted into the SDP following the date of the letter, HHS OIG requires a minimum
$50,000 settlement amount to resolve the matter. This provision would require that the Secretary,
in cooperation with the OIG, establish a self-referral disclosure protocol (SRDP) to enable health
care providers and suppliers to disclose actual or potential violations of the physician self-referral
law. In addition, the Secretary would be required to post information on CMS’ website to inform
stakeholders of how to disclose actual or potential SRDP violations. The CBO score is $0.0
billion for FY2010-FY2014 and $0.0 billion for FY2010-FY2019.

Sec. 6410. Adjustments to the Medicare Durable Medical Equipment, Prosthetics, Orthotics,
and Supplies Competitive Acquisition Program
. Medicare generally pays for most durable
medical equipment, prosthetics, orthotics and supplies (DMEPOS) on the basis of a fee schedule.
MMA required the Secretary to establish a Competitive Acquisition Program for specified
medical equipment in specified areas to replace the Medicare fee schedule. The program is to be
phased-in, starting in nine of the largest metropolitan statistical areas (MSAs) in 2009 (round 1);
expanding to an additional 70 of the largest MSAs in 2011 (round two) and remaining areas after
2011. The proposal would expand the number of areas included in round two of the program to
100 of the largest MSAs. The Secretary would extend the program, or apply competitively-bid
rates, to remaining areas by 2016. The CBO score is -$0.3 billion for FY2010-FY2014 and -$1.4
billion for FY2010-FY2019
.
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Sec. 6411. Expansion of the Recovery Audit Contractor (RAC) Program. Recovery Audit
Contractors, or RACs, are private organizations that contract with CMS to identify and collect
improper payments made in Medicare Parts A and B. Congress originally required the Secretary
to conduct a three-year demonstration program using RACs in the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA, P.L. 108-173). In December 2006,
Congress passed the Tax Relief and Health Care Act of 2006 (TRHCA, P.L. 109-432), which
made the program permanent and mandated the expansion of RACs nationwide by January 1,
2010. Medicare pays RACs differently than it pays other administrative contractors. Historically,
Medicare’s administrative contractors have been paid a fixed annual budget for a defined scope of
work. In contrast, Congress mandated that CMS pay RACs using contingency fees. A
contingency fee is a negotiated payment, typically a percentage, for every overpayment
recovered. This provision would require that the RAC program be expanded to Medicaid and
Medicare Parts C and D by December 2010. Among the requirements for Part C and D RACs,
would be ensuring that each MA or PDP plan have in place an anti-fraud plan, reviewing the
reinsurance payments of Part D plans, and comparing Part D plan’s enrollment estimates for high
cost beneficiaries. The CBO score is between -$50 million and +$50 million for FY2010-FY2014
and for FY2010-FY2019.37

Title IX—Revenue Provisions
Subtitle A—Revenue Offset Provisions
Sec. 9015. Additional Hospital Insurance Tax on High-Income Taxpayers. Under current law,
employees and employers each pay a payroll tax of 1.45% to finance Medicare Part A. The
Senate amendment would impose an additional tax of 0.5% on high-income workers with wages
over $200,000 for single filers and $250,000 for joint filers effective for taxable years after
December 31, 2012. Since employers would not know the wages of a spouse, they would be
directed to collect these revenues from all workers with wages exceeding $200,000 and then the
individuals would have to reconcile any excess withholding on their tax return. The 0.5% tax
would also be levied on the self-employed if their incomes exceed the specified thresholds. The
self-employed would not be allowed to deduct this additional tax as a business expense. The JCT
score is -$18.4 billion for FY2010-FY2014 and -$53.8 billion for FY2010-FY2019.



37 Provisions in Subtitle F regarding Medicaid program integrity will be discussed in an upcoming CRS report.
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Author Contact Information

Patricia A. Davis, Coordinator
Holly Stockdale
Specialist in Health Care Financing
Analyst in Health Care Financing
pdavis@crs.loc.gov, 7-7362
hstockdale@crs.loc.gov, 7-9553
Jim Hahn
Julie Stone
Analyst in Health Care Financing
Specialist in Health Care Financing
jhahn@crs.loc.gov, 7-4914
jstone@crs.loc.gov, 7-1386
Paulette C. Morgan
Sibyl Tilson
Specialist in Health Care Financing
Specialist in Health Care Financing
pcmorgan@crs.loc.gov, 7-7317
stilson@crs.loc.gov, 7-7368

Acknowledgments
Cliff Binder, Christopher Davis, Sarah Lister, Janemarie Mulvey, Amanda Sarata, and Jennifer Staman also
contributed to this report.

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