Medicare Fee-for-Service Modifications and Medicaid Provisions of H.R. 1 as Enacted
Congressional research reportJan 16, 2004
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Order Code RL32005
CRS Report for Congress
Received through the CRS Web
Medicare Fee-for-Service Modifications and
Medicaid Provisions of H.R. 1 as Enacted
Updated January 16, 2004
-name redacted-, Jennifer Boulanger, -name redacted
Steve Redhead, Evelyne Baumrucker, -name redacted-,
-name redacted-, and -name redactedSpecialists and Analysts in Social Legislation
Domestic Social Policy Division
Congressional Research Service ˜ The Library of Congress
Medicare Fee-for-Service Modifications and
Medicaid Provisions of H.R. 1 as Enacted
Summary
On November 22, the House of Representatives voted 220 to 215 to approve
the conference report on H.R. 1, the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003. The Senate, on November 24, voted 54 to 44 to approve
the conference report. Earlier, the conferees of the Medicare prescription drug and
modernization legislation announced an agreement on November 16 and the
legislative text was released November 20. The legislative language can be
downloaded from the House Committee on Ways and Means website at:
[http://waysandmeans.house.gov]. The bill was signed into law by the President on
December 8, 2003.
As well as establishing a prescription drug benefit for Medicare beneficiaries,
the legislation contains provisions that involving significant payment increases,
payment reductions, an expansion of covered benefits, new demonstration projects
and new beneficiary cost-sharing provisions for the traditional Medicare fee-forservice (FFS) program. The bill includes a measure that would require congressional
consideration of legislation if general revenue funding for the entire Medicare
program exceeds 45%. Provisions affecting the State Childrens’ Health Insurance
Program (SCHIP) and Medicaid programs are included in the legislation as well.
Earlier this year, under Congress’ FY2004 budget resolution, $400 billion was
reserved for Medicare modernization, creation of a prescription drug benefit, and, in
the Senate, to promote geographic equity payment. The Congressional Budget Office
(CBO) has estimated that the legislation for H.R. 1 would increase direct (or
mandatory) spending by $394.3 billion from FY2004 through FY2013. Prescription
drug spending is estimated at $409.8 billion over the 10-year period and Medicare
Advantage spending at $14.2 billion. Overall, the fee-for-service provisions which
change traditional Medicare are estimated to save $21.5 billion over the 10-year
period and adjusting the Part B premium to beneficiaries’ income is estimated to save
$13.3 billion over the period. Some fee-for-service provisions will increase spending
over this 10-year period including the provisions affecting hospitals and physician.
Other fee-for-service provisions are projected to save money over the period
including those affecting durable medical equipment, clinical laboratories and home
health agencies. The CBO estimate is available on the CBO website at
[ftp://ftp.cbo.gov/48xx/doc4808/11-20-MedicareLetter.pdf].
Contents
Changes to Medicare’s Fee for Service Program . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Selected Rural Provider Provisions . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Selected Acute Hospital Provisions . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Selected Physician Provisions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Selected Provisions Affecting Other Providers and Practitioners . . . . . 5
Selected Fee-for Service Demonstration Projects . . . . . . . . . . . . . . . . . 6
Expansion of Covered Benefits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Beneficiary Payments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Income-Relating the Part B Premium . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Indexing the Part B Deductible . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Medicaid and Miscellaneous Provisions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Modifications to Fee-for-Service Medicare . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Provisions Relating to Part A . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Hospital Services . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Allied Health and Graduate Medical Education Payments . . . . . . . . . 22
Skilled Nursing Facility (SNF) and Hospice Services . . . . . . . . . . . . . 25
Other Part A Provisions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Provisions Relating to Part B . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Physician and Practitioner Services . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Hospital Outpatient Department (HOPD), Ambulatory Surgery
Center (ASC), and Clinic Services . . . . . . . . . . . . . . . . . . . . . . . 42
Covered Part B Outpatient Drugs (Not Provided by a HOPD) . . . . . . 48
Covered Drugs and Services at a Dialysis Facility . . . . . . . . . . . . . . . 57
Durable Medical Equipment (DME) and Related Outpatient Drugs . . 58
Ambulance Services . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Other Part B Services and Provisions . . . . . . . . . . . . . . . . . . . . . . . . . 65
Provisions Relating to Parts A and B . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69
Home Health Services . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69
Chronic Care Improvement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Medicare Secondary Payor (MSP) . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Other Medicare A and B Provisions . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Medicare Demonstration Projects and Studies . . . . . . . . . . . . . . . . . . 82
Beneficiary Issues: Cost-Sharing Amounts and Provision of Information . 90
Other Health-Related Studies, Commissions or Committees . . . . . . . . . . . 94
Medicaid and State Children’s Health Insurance Program (SCHIP)
Provisions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99
Cost Containment and Miscellaneous Financial Provisions . . . . . . . . . . . 106
Medicare Fee-for-Service Modifications
and Medicaid Provisions of
H.R. 1 as Enacted
On November 22, 2003, the House of Representatives voted 220 to 215 to
approve the conference report on H.R. 1, the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003. The Senate, on November 24th,
voted 54 to 44 to approve the conference report. The bill was signed by the President
in a ceremony on December 8th. The legislation adds a prescription drug benefit to
Medicare and replaces the existing Medicare+Choice program with a new
MedicareAdvantage program that establishes managed care payments based on a
system of bids and benchmarks. The bill also contains numerous provisions that
would generally increase fee-for-service payments within Medicare’s Part A and Part
B program (also known as traditional Medicare), especially for rural health care
providers; numerous regulatory and administrative practices will also be modified.
This report discusses the fee-for-service (FFS) provisions of the legislation, those
affecting Medicaid as well as the Medicare cost containment provisions1. It
compares the provisions in the bill as enacted with those in the Medicare reform bills
that were originally passed by the Senate and the House.
The Medicare FFS provisions in the bill are found primarily in Titles GGIII
through VIII; some FFS provisions are included in Titles VIII through X as noted.
The cost containment provisions are in Title VIII and the Medicaid and other
provisions are in Title X. An overview of the entire legislation can be found in CRS
Report RL31966.
Changes to Medicare’s Fee for Service Program
The legislation contains extensive changes to Medicare’s FFS program,
including payment increases and, in certain instances, decreases; development of
competitive acquisition programs; implementation or refinement of other prospective
payment systems (notably, the development of an end-stage renal disease (ESRD)
basic payment system); expansion of covered preventive benefits; establishment of
demonstration programs; and required studies. The anticipated financial impact of
these changes on any individual provider, physician, or supplier will vary depending
on many factors, such as the unique characteristics of the individual or entity
participating in Medicare as well as the number and type of services provided to the
1
Cost containment provisions require an analysis of general tax revenue financing of the
Medicare program as well as a Presidential and Congressional response when “excess
general revenue financing of Medicare” exceeds a threshold of 45%.
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Medicare beneficiaries they serve. Selected highlights of the FFS payment
provisions and those establishing preventive care benefits and demonstration
programs will be briefly described.
Selected Rural Provider Provisions.
Generally, Medicare payments to certain rural providers are expected to
increase; many of the rural provisions will benefit urban providers as well. CBO
estimates that the rural provisions in Title IV of the bill will increase Medicare’s
direct spending by $9.3 billion from 2004 through 2008 and by $19.9 billion from
2004 though 2013. It should be noted that other provider payment provisions in H.R.
1 can impact rural providers, but their effect on Medicare payments to rural providers
has not been specifically identified.
Hospitals in rural areas and those in small urban areas will receive
a permanent 1.6% increase to Medicare’s base rate or per discharge
payment; the payment limit for rural and small urban hospitals that
qualify for disproportionate share hospital (DSH) adjustment will
increase from 5.25% to 12%; hospitals in low-wage areas (those
with wage index values below 1) will receive additional payments
through a decrease from 71% to 62% in the labor-related portion of
the base payment rate; and small rural hospitals with less than 50
beds will receive cost reimbursement for outpatient clinical
laboratory tests. In addition, rural hospitals with less than 100 beds
will be protected from payment declines associated with the hospital
outpatient prospective payment system (OPPS) for an additional 2
years; these OPPS hold harmless provisions will be extended to sole
community hospitals for services from 2004 through 2006. CBO
estimates that these provisions will increase direct Medicare
spending by $15.6 billion over the 10-year period.
! Critical access hospitals (CAHs) will have their bed limit increased
from 15 to 25; there will be no restriction on the number of these
beds that can be used for acute care services at any one time. CAHs
will be able to establish distinct part rehabilitation and psychiatric
units of up to 10 beds that will not be included in the CAH bed
count. Cost reimbursement of CAH services will increase to 101%
of reasonable costs, starting January 1, 2004. Periodic interim
payments for CAHs will be authorized. State authority to waive the
35-mile requirement for new entities to qualify as a CAH will be
eliminated as of January 1, 2006. CBO estimates that these
provisions will increase direct Medicare spending by $900 million
over the 10-year period.
! Physicians in newly established scarcity areas will receive a 5%
increase in Medicare payments. Physicians in certain low-cost areas
with geographic adjustment factors below 1 will receive payment
increases so as to increase this factor to 1, starting in 2004 through
2006. CBO estimates that these provisions will increase direct
Medicare spending by $1.7 billion over the 10-year period.
! Practitioners in rural health clinics and federally qualified health
centers will be able to bill separately for services provided to
!
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beneficiaries in skilled nursing facilities. CBO estimates that these
provisions will increase direct Medicare spending by $100 million
over the 10-year period.
! Home health providers in rural areas will receive a 5% increase in
Medicare payments for one year beginning April 1, 2004. CBO
estimates that this one-year increase will increase direct Medicare
spending by $100 million over the 10-year period.
Selected Acute Hospital Provisions.
Generally, Medicare payments to hospitals will increase under the conference
report. Specifically,
Acute hospitals paid under the inpatient prospective payment system
(IPPS) will receive the full increase in the market basket (MB) index
as an update in 2004. From 2005 through 2007, hospitals that
submit data on specified quality indicators will receive the MB as an
update; those hospitals that do not submit such data will receive the
MB minus 0.4 percentage points for the year in question. CBO
expects that this provision will reduce direct spending 0.2 billion
from 2004 through 2008.
! Teaching hospitals will receive an increase in their indirect medical
education adjustment from 2004 through 2006 that CBO projects
will increase spending by $400 million.
! A one-time, geographic reclassification process to increase
hospitals’ wage index values for 3 years that is expected to increase
payments by $900 million from 2004 through 2008 is established.
! Low volume hospitals with fewer than 800 discharges that are 25
road miles away from similar hospitals may qualify for up to a 25%
increase in Medicare payments for an expected cost of $100 million
from 2004-2013.
! Changes in payment methods for covered prescription drugs
provided in outpatient hospital departments is expected to increase
payments by $700 million from FY2004 through FY2008.
! A redistribution of unused resident positions will increase both
direct and indirect graduate medical education spending by an
anticipated $200 million from FY2004 thought FY2008 and by $600
million from FY2004 through FY2013.
! Certain teaching hospitals with high per resident payments will not
receive a payment increase from FY2004 through FY2013; this
provision was scored by CBO as a reduction in Medicare spending
of $500 million from FY2004 through FY2008 and $1.3 billion from
FY2004 through FY2013.
! For 18 months from the date of enactment, physicians will not be
able to refer Medicare patients to specialty hospitals in which they
have an investment interest. This provision will not apply to
hospitals that are in operation or under development before
November 18, 2003. Both MedPAC and HHS are to complete
required studies on specialty hospitals within 15 months of
enactment.
!
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Selected Physician Provisions.
The impact of the legislation on Medicare’s spending for physician spending is
difficult to determine. Although physicians will receive a 1.5% update in 2004 and
2005 which is expected to increase spending by $2.8 billion from FY2004 through
FY2007; subsequently, from FY2008 through FY2012, the provision is expected to
result in a decline of $2.8 billion in Medicare spending. Over the 10 year period
from 2004 through 2013, CBO expects the update provisions to increase Medicare
spending by $200 million.
Medicare’s payments for some practice expenses, particularly the administration
of covered drugs, will increase starting in 2004. A transitional adjustment to the drug
administration payments of 32% in 2004 and 3% in 2005 is also established. These
payment increases are expected to be counterbalanced by a decrease in Medicare’s
payments for covered outpatient drugs provided in a doctor’s office.
Medicare’s payment for covered outpatient drugs furnished incident to a
physician’s service will change during 2004 as follows:
Many covered outpatient drugs furnished in 2004 will be reimbursed
at 85% of the average wholesale price (AWP). Certain of these
drugs may be paid as low as 80% of the AWP (in effect as of April
1, 2003).
! Blood clotting factors and other blood products, drugs or biologicals
(drug products) that were not available for payment by April 1,
2003, covered vaccinations, drug products furnished in during 2004
in connection with renal dialysis services, drugs provided through
covered durable medical equipment will be paid at a higher rate
during 2004.
!
The decline in payments for covered outpatient drugs in 2004 can only be
implemented concurrently with the increased payments for the administration of the
drugs.
Starting in 2005, Medicare’s payment for many covered outpatient drugs will
be based on average sales price methodology, that uses different pricing and cost
data, depending on the prescription drug. Generally, multiple source drugs will be
paid 106% of the average sales price; single source drugs will be paid 106% of the
lower of the average sales price or the wholesale acquisition costs, unless the widely
available market price or the average manufacturer price for those drugs exceeds a
certain threshold. Starting in 2006, physicians will have the option of obtaining
covered Part B drugs from selected entities awarded contracts for competitively
biddable drug products under a newly established competitive acquisition program.
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Selected Provisions Affecting Other Providers and Practitioners.
The follow provisions affecting other providers and practitioners are included
in the legislation:
Ambulatory Surgical Centers. Payments to ambulatory surgical centers
(ASCs) are expected to be lower by $800 million from FY2004 through FY2008 and
by $3.1 billion from FY2004 through FY2013 as a result of the legislation. ASCs
will receive an update of the consumer price index for all urban consumers (CPI-U)
minus 3.0 percentage points starting April 1, 2004 and will receive a O percent
update for services provided starting October 1, 2004 through December 31, 2009.
Therapy Caps. Application of the caps on outpatient therapy services
provided by non-hospital providers is suspended from the date of enactment and for
the remainder of 2003, in 2004 and 2005. CBO estimates that the therapy cap
moratorium will increase direct Medicare spending by $700 million over the 10-year
period.
Durable Medical Equipment (DME). Competitive bidding for DME will
be phased-in beginning in 2007 in 10 of the largest metropolitan statistical areas and
may be phased in first for the highest cost and highest volume items and services.
The update for most DME items and services and for prosthetics and orthotics is 0
in 2004, 2005, 2006, 2007, and 2008. For 2005, payment for certain items, oxygen
and oxygen equipment, standard wheelchairs, nebulizers, diabetic lancets and testing
strips, hospital beds and air mattresses will be reduced by an amount calculated using
2002 payment amounts and the median price paid by the Federal Employees Health
Benefit Program.2 Beginning January 1, 2009, items and services included in the
competitive acquisition program will be paid as determined under that program and
the Secretary can use this information to adjust the payment amounts for DME, offthe-shelf orthotics, and other items and services that are supplied in an area that is not
a competitive acquisition area. Class III items (devices that sustain or support life,
are implanted, or present potential unreasonable risk, e.g., implantable infusion
pumps and heart valve replacements, and are subject to premarket approval, the most
stringent regulatory control) receive the full increase in the consumer price index for
all urban consumers (CPI-U) in 2004, 2005, 2006 , 2008 and subsequent years. The
Secretary will determine the update in 2007. CBO scored the DME provisions of
the bill as reducing spending by $6.8 billion over the 10-year period.
Home Health. Home health agency payments are increased by the full market
basket percentage for the last quarter of 2003 (October, November, and December)
and for the first quarter of 2004 (January, February, and March). The update for the
remainder of 2004 and for 2005 and 2006 is the home health market basket
percentage increase minus 0.8 percentage points. CBO estimates that this provision
2
Section 302 specifies that the reduction uses the “Median FEHP Price” in the table entitled
“Summary of Medicare Prices Compared to VA, Medicaid, Retail, and FEHB Prices for 16
Items” that was included in testimony of the Health and Human Services Inspector General
before the Senate Committee on Appropriations, June 12, 2002, or any subsequent report
by the Inspector General.
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will reduce direct Medicare spending by $6.5 billion over the 10-year period. The
legislation suspends the requirement that home health agencies must collect the
Outcome and Assessment Information Set (OASIS) data on private pay (nonMedicare, non-Medicaid) until the Secretary reports to Congress and publishes final
regulations regarding the collection and use of OASIS.
Selected Fee-for Service Demonstration Projects.
The legislation establishes numerous demonstration projects for the Medicare
program. Several demonstrations address aspects of disease management for
beneficiaries with chronic conditions.
Chronic Care Improvement under Fee-For-Service. The legislation
requires the Secretary to establish and implement chronic care improvement
programs under fee-for-service Medicare to improve clinical quality and beneficiary
satisfaction and achieve spending targets specified by the Secretary for Medicare for
beneficiaries with certain chronic health conditions. Participation by beneficiaries
is voluntary. The contractors are required to assume financial risk for performance
under the contract. CBO has estimated that this demonstration will increase direct
Medicare spending by $500 million over the 10-year period.
Chronically Ill Beneficiary Research, Demonstration. The legislation
requires the Secretary to develop a plan to improve quality of care and to reduce the
cost of care for chronically ill Medicare beneficiaries within 6 months after
enactment. The plan is required to use existing data and identify data gaps, develop
research initiatives, and propose intervention demonstration programs to provide
better health care for chronically ill Medicare beneficiaries. The Secretary is required
to implement the plan no later than 2 years after enactment.
Coverage of Certain Drugs and Biologicals Demonstration. The
Secretary is required to conduct a 2-year demonstration where payment is made for
certain drugs and biologicals that are currently provided as “incident to” a physician’s
services under Part B. The demonstration is required to provide for cost-sharing in
the same manner as applies under Part D of Medicare. The demonstration is required
to begin within 90 days of enactment and is limited to 50,000 Medicare beneficiaries
in sites selected by the Secretary.
Homebound Demonstration. The Secretary is required to conduct a 2-year
demonstration project where beneficiaries with chronic conditions would be deemed
to be homebound in order to receive home health services under Medicare.
Adult Day Care. The Secretary is required to establish a demonstration where
beneficiaries could receive adult day care services as a substitute for a portion of
home health services otherwise provided in a beneficiary’s home.
Expansion of Covered Benefits.
The legislation contains a number of provisions that expand coverage beginning
January 1, 2005, including the following:
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Initial Physical Examination. Medicare coverage of an initial preventive
physical examination is authorized for those individuals whose Medicare coverage
begins on or after January 1, 2005. CBO estimates that this provision will increase
direct Medicare spending by $1.7 billion over the 10-year period.
Cardiovascular Screening Blood Tests. Medicare coverage of
cardiovascular screening blood tests is authorized. CBO estimates that this provision
will increase direct Medicare spending by $300 million over the 10-year period.
Diabetes Screening Tests. Diabetes screening tests furnished to an
individual at risk for diabetes for the purpose of early detection of diabetes are
included as a covered medical service. In this instance, diabetes screening tests
include fasting plasma glucose tests as well as other tests and modifications to those
tests deemed appropriate by the Secretary. CBO estimates that this provision will
increase direct Medicare spending less than $50 million over the 10-year period.
Screening and Diagnostic Mammography. Screening mammography
and diagnostic mammography will be excluded from OPPS and paid separately.
CBO estimates that this provision will increase direct Medicare spending by $200
million over the 10-year period.
Intravenous Immune Globulin. The bill includes intravenous immune
globulin for the treatment in the home of primary immune deficiency diseases as a
covered medical service under Medicare. CBO estimates that this provision will
increase direct Medicare spending by $100 million over the 10-year period.
Beneficiary Payments
The bill contains two provisions which change the beneficiary premiums and
deductibles.
Income-Relating the Part B Premium.
The legislation increases the monthly Part B premiums for higher income
enrollees beginning in 2007. Beneficiaries whose modified adjusted gross income
exceed $80,000 and couples filing joint returns whose modified adjusted gross
income exceeds $160,000 will be subject to higher premium amounts. The increase
will be calculated on a sliding scale basis and will be phased-in over a five-year
period. The highest category on the sliding scale is for beneficiaries whose modified
adjusted gross income is more than $200,000 ($400,000 for a couple filing jointly).
Those amounts are increased beginning in 2007 by the percentage change in the
consumer price index. CBO estimates that direct Medicare spending will be reduced
by $13.3 billion over the 10-year period 2004 through 2013.
Indexing the Part B Deductible.
The Medicare Part B deductible will remain $100 through 2004, increase to
$110 for 2005, and in subsequent years the deductible will be increased by the same
CRS-8
percentage as the Part B premium increase. Specifically, the annual percentage
increase in the monthly actuarial value of benefits payable from the Federal
Supplementary Medical Insurance Trust Fund will be used as the index.
Medicaid and Miscellaneous Provisions
Title X of the legislation makes some changes to Medicaid and other programs.
Omitted from the agreement were two provisions contained in S. 1, including a
provision to amend the Age Discrimination in Employment Act of 1967 to allow an
employee benefit plan to offer different benefits to their Medicare eligible employees
than to their non-Medicare eligible employees, and a provision to allow states to
cover certain lawfully residing aliens under the Medicaid program.
CBO estimates the Medicaid and other provisions included in the bill to increase
direct spending by $5.7 billion between FY2004 and FY2013. The following general
points can be made about the Medicaid and Miscellaneous provisions included in
Title X of the bill:
The legislation temporarily increases states’ disproportionate share
hospital (DSH) allotments to erase the decline in these Medicaid
amounts that occurred after a special rule for their calculation
expired.
! The legislation includes several other Medicaid provisions, including
raising the floor on DSH allotments for “extremely low DSH states,”
providing DSH allotment adjustments impacting Hawaii and/or
Tennessee, increasing reporting requirements for DSH hospitals, and
exempting prices of drugs provided to certain safety net hospitals
from Medicaid’s best price drug program.
! Miscellaneous provisions in Title X of the legislation include
funding federal reimbursement of emergency health services
furnished to undocumented aliens, and funding administrative startup costs for Medicare reform, various research projects, work groups
and infrastructure improvement programs for the health care system.
!
This report contains a detailed side-by-side comparison of the relevant
provisions of the legislation, S. 1, as passed the Senate, and H.R. 1, as passed the
House. Certain of the provisions can be found in one or more of the sections. For
example, the home health homebound demonstration (section 702) is listed in the
home health section and the demonstration projects section. Also included in this
side-by-side, are provision that were included in the House and/or Senate bill which
were dropped in conference.
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Modifications to Fee-for-Service Medicare
Provisions Relating to Part A
Hospital Services.
Provision and Current Law Description
Increase standardized amounts for small
urban and rural hospitals in Medicare’s
inpatient hospital prospective payment
system (IPPS).
Medicare pays for
inpatient services in acute hospitals in
large urban areas using a standardized
amount that is 1.6% larger than the
standardized amount used to reimburse
hospitals in other areas (both rural areas
and smaller urban areas). P.L. 108-7
provided that all Medicare discharges from
April 1, 2003 to September 30, 2003, will
be paid on the basis of the large urban area
amount. The Secretary is authorized to
delay implementation of this payment
increase until November 1, 2003, if
necessary.
Under Medicare’s IPPS, two
different standardized amounts are used for
hospitals in Puerto Rico, one for hospitals
in large urban areas and one for other
hospitals.
Increase payments to hospitals in areas
with wage index values below one (by
lowering Medicare’s IPPS labor-related
share which is the proportion of the
standardized amount multiplied by the
wage index). IPPS payments are adjusted,
H.R. 1 as enacted
S. 1 (as passed the Senate)
Inpatient Prospective Payment System (IPPS) Hospitals
Medicare would pay
Section 401. Medicare will pay hospitals Section 401.
in rural and small urban areas in the 50 hospitals in rural and small urban areas in
states using the standardized amount that the fifty states using the standardized
would be used to pay hospitals in large amount used to pay hospitals in large
urban areas starting for discharges in urban areas starting for discharges in
FY2004. The existing authority of the FY2004. The Secretary would compute
Secretary to delay implementation of this one standardized amount for hospitals in
increase until November 1, 2003 for Puerto Rico equal to that for other areas.
hospitals that are not in Puerto Rico is not
affected. The Secretary will compute one
local standardized amount for all hospitals
in Puerto Rico equal to that for hospitals in
large urban areas in Puerto Rico starting
for discharges in FY2004. Hospitals in
Puerto Rico will receive the legislated
payment increase starting for discharges on
April 1, 2004.
Section 403. For discharges on or after
October 1, 2004, the Secretary is required
to decrease the labor-related share to 62%
of the standardized amount when such
change will result in higher total payments
to the hospital. This provision is to be
Section 402. For cost reporting periods
beginning October 1, 2004, the Secretary
would be required to decrease the laborrelated share to 62% of the standardized
amount only if such change would result in
higher total payments to the hospital. This
H.R. 1 (as passed the House)
Section 402.
Similar provision with
respect to discharges in the fifty states.
Two standardized amounts would still be
used for hospitals in Puerto Rico; one
federal amount would be used in the
calculation of these 2 rates.
Section 416. Same provision except that
the effective date is October 1, 2003.
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Provision and Current Law Description
H.R. 1 as enacted
S. 1 (as passed the Senate)
either increased or decreased as
appropriate, by the hospital wage index of
the area where the hospital is located or
where it has been reassigned. Presently,
approximately 71% of the standardized
amount is adjusted by the area wage index.
applied without regard to certain budgetneutrality requirements. For discharges on
or after October 1, 2004, the Secretary is
also required to decrease the labor-related
share to 62% of the standardized amount
for hospitals in Puerto Rico when such
change results in higher total payments to
the hospital.
Section 406. The Secretary is required to
provide for a graduated adjustment of up to
25% of Medicare’s inpatient payment rates
to account for the empirically established
higher unit costs associated with lowvolume hospitals starting for discharges
occurring in FY2005. A low-volume
hospital is a short-term general hospital
that is located more than 25 road miles
from another such hospital and that has
less than 800 discharges during the fiscal
year. Certain budget neutrality
requirements would not apply to this
provision. The determination of the
percentage payment increase is not subject
to administrative or judicial review.
provision would be applied without regard
to certain budget neutrality requirements.
Increase Medicare IPPS payments for
low-volume hospitals. Medicare pays
inpatient acute hospital services for each
discharge from the hospital without regard
to the number of beneficiaries discharged
from any given hospital. Under certain
circumstances, however, sole community
hospitals (SCHs) and Medicare dependent
hospitals with more than a 5% decline in
total discharges from one period to the
next may apply for an adjustment to their
payment rates to partially account for
higher costs associated with a drop in
patient volume due to circumstances
beyond their control.
Increase disproportionate share hospital
(DSH) payments for small urban and
rural hospitals.
Medicare makes
additional payments to certain acute
hospitals that serve a large number of lowincome Medicare and Medicaid patients.
Although a SCH or rural referral center
(RRC) can qualify for a higher DSH
adjustment, generally, the DSH adjustment
Section 402. Starting for discharges after
April 1, 2004, a hospital that is not a large
urban hospital that qualifies for a DSH
adjustment will receive its DSH payments
using the current DSH adjustment formula
for large urban hospitals, subject to a limit.
The DSH adjustment for any of these
hospitals, except for rural referral centers,
will be capped at 12%. A Pickle hospital
Section 403. The Secretary would be
required to develop a graduated adjustment
of up to 25% of Medicare’s inpatient
payment rates to account for the higher
unit costs in low-volume hospitals. Certain
hospitals with fewer than 2,000 total
discharges during the three most recent
cost reporting periods would be eligible for
up to a 25% increase in their Medicare
payment amount starting with cost reports
that begin during FY2005.
Eligible
hospitals would be located at least 15 miles
from a similar hospital or those determined
by the Secretary to be so located due to
factors such as weather conditions, travel
conditions, or travel time to the nearest
alternative source of appropriate inpatient
care. Certain budget neutrality
requirements would not apply.
Section 404. Starting for discharges after
October 1, 2004, a hospital that qualifies
for a DSH adjustment when its DSH
patient percentage exceeds the 15% DSH
threshold would receive the DSH payments
using the current formula that establishes
the DSH adjustment for a large urban
hospital.
H.R. 1 (as passed the House)
No provision.
Section 401. Starting for discharges after
October 1, 2003, a hospital that is not a
large urban hospital that qualifies for a
DSH adjustment would receive its DSH
payments using the current DSH
adjustment formula for large urban
hospitals, subject to a limit. The DSH
adjustment for any of these hospitals,
except for RRCs, would be capped at 10%.
CRS-11
Provision and Current Law Description
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
that a small urban or rural hospital can
receive is limited to a maximum of a
5.25% increase to its IPPS payment. Large
(100 beds and more) urban hospitals and
large rural hospitals (500 beds and more)
are eligible for a higher adjustment that
can be significantly greater; the amount of
the DSH adjustment received by these
larger hospitals will depend upon its DSH
patient percentage (the percentage of lowincome Medicare or Medicaid patients
served).
Require MedPAC report on Medicare
DSH adjustments.
No provision in
current law.
receiving a DSH adjustment under the
alternative formula will not be affected by
this provision. (For a description of Pickle
hospitals, see page 12 column 1.)
No provision.
Section 404A.
MedPAC would be
required to conduct a study to determine
(1) whether DSH payments should be
made in the same manner as Medicare’s
graduate medical education payments; (2)
the extent that hospitals receiving
Medicaid DSH payments also receive
Medicare DSH payments; and (3) whether
uncompensated care costs should be added
to the Medicare DSH formula. The report,
including recommendations, would be due
to Congress within 1 year from enactment.
No provision.
Exclude wage data of hospitals that
convert to critical access hospitals
(CAHs) from IPPS wage index. Certain
qualified small hospitals are converting to
CAHs. After conversion, these facilities
are paid on a reasonable cost basis and are
not paid under IPPS. Medicare’s IPPS
payments to acute hospitals are adjusted by
the wage index of the area where the
hospital is located or has been reassigned.
Although the hospital wage index is
No provision.
Section 405(e). The Secretary would be
required to exclude wage data from
hospitals that have converted to CAHs
from the IPPS wage index calculation
starting for cost reporting periods
beginning January 1, 2004.
No provision.
CRS-12
Provision and Current Law Description
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
recalculated annually, the wage index for
any given fiscal year is based on data
submitted as part of a hospital’s cost report
from 4 years previously. As of FY2004,
wage data from hospitals that have
converted to CAHs were excluded from
the IPPS wage index calculation.
Increase DSH for “Pickle” hospitals.
Most DSH hospitals receive additional
Medicare payments because they serve a
disproportionate share of poor Medicare
and Medicaid patients. A few urban
hospitals receive DSH payments under an
alternative Pickle formula. If a hospital
receives at least 30% of its patient care
revenue from indigent care funds, it will
get a 35% increase in its Medicare
operating payments. The Pickle hospitals
receive a capital DSH adjustment of
14.16%, the amount that other non-Pickle
hospitals with a 35% operating DSH
adjustment would receive.
No provision.
Section 420A. Hospitals that qualify for
the DSH adjustment under the Pickle
amendment would receive a DSH
operating and capital adjustment of 40%
for discharges beginning October 1, 2003.
No provision.
Increase payments for hospitals in
Puerto Rico. Under Medicare’s IPPS,
separate standardized amounts are used to
pay short-term general hospitals in Puerto
Rico. The Balanced Budget Act of 1997
(BBA 97) provides for an adjustment of
the Puerto Rico rates from blended
amounts based on 25% of the national
amounts and 75% of the local amounts to
blended amounts based on a 50/50 split
between national and local amounts.
Section 504. Hospitals in Puerto Rico will
receive Medicare payments based on a
50/50 split between federal and local
amounts before April 1, 2004. Starting
April 1, 2004 through September 30, 2004,
payment will be based on 62.5% national
amount and 37.5% local amount; this will
change to 75% national and 25% local
after October 1, 2004 and in subsequent
years.
Section 409. Hospitals in Puerto Rico
would receive Medicare payments based
on a 50/50 split between national and local
amounts before October 1, 2004. These
hospitals would receive Medicare
payments based on 100% of the federal
rate for discharges beginning October 1,
2004 and before October 1, 2009. The rate
for hospitals in Puerto Rico would revert to
a 50/50 split after October 1, 2009.
Section 503. From FY2004 though
FY2007, hospitals in Puerto Rico would
receive an increasing amount of the
payment rate based on national rates as
follows: during FY2004, payment would
be 59% national and 41% local; during
2005, payment would be 67% national
and 33% local and 75% national and 25%
local during FY2006 and subsequently.
CRS-13
Provision and Current Law Description
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Require GAO report on appropriateness
of IPPS payments. No provision in
current law.
No provision.
Section 413. Using the most current data,
the Comptroller General (GAO) would be
required to report to Congress within 18
months of enactment on:
(1) the
appropriate level and distribution of IPPS
Medicare payments to short-term general
hospitals; and (2) the need for geographic
adjustments to reflect legitimate
differences in hospital costs.
No provision.
Calculate wage indices for hospitals.
IPPS hospitals may apply to the Medicare
Geographic Classification Review Board
(MGCRB) for a change in classification to
a different area. If reclassification is
granted, the new wage index will be used
to calculating Medicare’s payment for
inpatient and outpatient services. The
reclassification standards are established
by regulation.
Section 508. The Secretary will establish
a wage index appeals process by January 1,
2004. A hospital seeking to be reclassified
must submit an appeal to the MGCRB no
later than February 15, 2004.
Reclassifications will be effective for a 3year period starting April 1, 2004. There
will be no further administrative or judicial
review of these decisions. The additional
spending associated with this provision
cannot exceed $900 million.
Section 404. The Secretary is required to
revise the market basket weights to reflect
the most currently available data and to
establish a schedule for revising the cost
category weights more often than once
every 5 years. The Secretary is required to
publish the reasons for and the options
considered in establishing such a schedule
in the final rule establishing FY2006
inpatient hospital payments.
Section 419. The Secretary would be able
to waive established reclassification
criteria in calculating the wage index in a
state when making payments for hospital
discharges in FY2004.
No provision.
No provision
Section 404. The Secretary would be
required to revise the market basket cost
weights to reflect the most currently
available data and to establish a schedule
for revising the weights more often than
once every 5 years. The Secretary would
be required to submit a report to Congress
by October 1, 2004 on the reasons for and
the options considered in establishing such
a schedule.
Update hospital market basket more
frequently. IPPS standardized amounts
are increased annually using an update
factor which is determined in part by the
projected increase in the hospital market
basket (MB), an input price index which
measures the average change in the price
of goods and services hospitals purchased
in order to furnish inpatient care. Centers
for Medicare and Medicaid Services
(CMS) revises the category weights,
reevaluates the price proxies for such
categories, and rebases the MB every 5
years.
CRS-14
Provision and Current Law Description
H.R. 1 as enacted
Reduce hospital update factor. Each
year, Medicare’s operating payments to
hospitals are increased or updated by a
factor that is determined in part by the
projected annual change in the hospital
MB. Congress establishes the update for
Medicare’s IPPS for operating costs, often
several years in advance. Currently, acute
care hospitals will receive the MB as an
update for FY2004 and subsequently.
Section 501. Acute hospitals will receive
the MB as the operating update for
FY2004. From FY2005 through FY2007,
hospitals that submit required quality data
will receive the MB as an update;
hospitals that do not submit such data will
receive the MB minus 0.4 percentage
points. The reduction would apply to the
year in question only and would not be
taken into account in subsequent years.
The operating update will be the MB in
FY2008 and in subsequent years.
Section 503. The Secretary is required to
add new diagnosis and procedure codes in
April 1 of each year but is not required to
change Medicare’s payment or DRG
classification as a result of these additions
until the fiscal year that begins after that
date. When establishing whether DRG
payments are inadequate, the Secretary is
required to apply a threshold that is the
lesser of 75% of the standardized amount
(increased to reflect the difference between
costs and charges) or 75% of one standard
deviation for the DRG involved. The
Secretary is required to: (1) maintain a
current public list of pending applications
for this additional payment; (2) accept
public comment, recommendations, and
data regarding whether a service or
technology represents a substantial
improvement; and (3) provide for a public
meeting with the clinical staff at CMS and
organizations representing physicians,
beneficiaries, manufacturers or other
interested parties. These actions will occur
Increase pass-through payments for new
inpatient technology. The Medicare,
Medicaid, and SCHIP Benefits
Improvement and Protection Act of 2000
(BIPA) established that Medicare’s IPPS
should recognize the costs of new medical
services and technologies beginning
October 1, 2001. The additional hospital
payments can be made by the means of
new technology groups, an add-on
payment, a payment adjustment, or other
mechanism, but cannot be a separate fee
schedule and must be budget neutral. CMS
established that a technology that provided
a substantial improvement to existing
treatments would qualify for additional
payments. The add-on payment for an
eligible new technology would occur when
the standard diagnosis related group
(DRG) payment was inadequate. This
threshold was established as one standard
deviation above the mean standardized
DRG; the add-on payment for new
technology would be the lesser of: (a) 50%
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
No provision.
Section 501. Acute hospitals would
receive an operating update of the MB
minus 0.4 percentage points for FY2004
through FY2006. The operating update
would be the MB increase in FY2007 and
subsequently.
No provision.
Section 502. New diagnosis and procedure
codes would be added in April 1 of each
year that would affect Medicare’s IPPS
starting the following October. The
Secretary would not be able to deny new
technology status because an item has been
used prior to the 2-to-3 year period before
it was issued a billing code. When
establishing whether DRG payments are
inadequate, the Secretary would be
required to apply a threshold that is the
lesser of 75% of the standardized amount
(adjusted to reflect the difference between
costs and charges) or 75% of one standard
deviation for DRG involved.
The
Secretary would be required to provide
additional regulatory guidance on the new
technology criteria. The Secretary would
be required to deem that a technology
provides a substantial improvement on an
existing treatment if it is designated under
section 506 of the FDA Act, approved
under certain sections of Title 21,
designated for priority review, is an
CRS-15
Provision and Current Law Description
H.R. 1 as enacted
of the costs of the new technology; or (b)
50% of the amount by which the costs
exceeded the standard DRG payment.
However, if the new technology payments
are estimated to exceed the budgeted target
amount of 1% of the total operating
inpatient payments, the add-on payments
are reduced prospectively. CMS has
proposed to reduce the threshold to 75% of
one standard deviation beyond the
geometric mean standardized charge for all
cases in the DRG to which the new service
is assigned.
prior to the publication of a proposed
regulation. Before establishing an add-on
payment as the appropriate reimbursement
mechanism, the Secretary is directed to
identify one or more DRGs and assign the
technology to that DRG. When such
assignment to a DRG occurs, no add-on
payment would be made; the budgetneutrality requirement with respect to
annual DRG reclassifications and
recalculation will apply. Funding for new
technology is no longer required to be
budget neutral. The provisions will apply
to new technology determinations
beginning in FY2005. Applications that
were denied in FY2005 will be
reconsidered under these provisions; if
granted, the maximum time period
otherwise permitted for such classification
as a new technology is extended by 12
months.
Section 505. The Secretary is required to
establish an application process and 3-year
payment adjustment to recognize the outmigration of hospital employees who
reside in a county and work in a different
area with a higher wage index. A hospital
that receives such a payment adjustment
will be located in a qualifying county that
meets certain criteria including (1) a
threshold of no less than 10% for
minimum out-migration to a higher wage
index area or areas, and (2) a requirement
that the average hourly wage of the
hospitals in the qualifying county equals or
exceeds the average hourly wage of all the
Increase hospitals’ wage index values to
reflect commuting patterns from higher
wage index areas. Unlike other providers,
IPPS hospitals may apply to the Medicare
Geographic Classification Review Board
(MGCRB) for reassignment to another
area. The MGCRB was created to
determine whether a hospital should be
redesignated to an area with which it has
close proximity for purposes of using the
other area’s wage index. A hospital can
establish proximity to the new area by
documenting that at least 50% of its
employees reside there. Other cost criteria
must be met before a hospital will be
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
exempt medical device under section
520(m) of such Act, or receives expedited
review under section 515(d)(5). Other
requirements requiring the process for
public input would be imposed. A
preference fo use of a DRG adjustment
would be established. Add-on payments
would be increased to the percentage that
Medicare reimburses inpatient outlier
cases. Funding for this new technology
would no longer be budget neutral.
No provision.
Section 504. The Secretary would be
required to establish an application process
and payment adjustment to recognize the
commuting patterns of hospital employees.
A hospital that qualified for such a
payment adjustment would have average
hourly wages that exceed the average
wages of the area in which it is located and
have at least 10% of its employees living
in one or more areas that have higher wage
index values. The process would be based
on the MGCRB reclassification process
and schedule with respect to data
submitted. Such an adjustment would be
effective for 3 years unless a hospital
CRS-16
Provision and Current Law Description
H.R. 1 as enacted
reclassified. If reclassification is granted,
the wage index for the new area will be
used to calculate Medicare’s payment for
inpatient and outpatient services provided
by the hospital.
hospitals in the area where the county is
located. The Secretary may require acute
hospitals and other hospitals as well as
critical access hospitals to submit data
regarding the location of their employees’
residence or the Secretary may use data
from other sources. A hospital that receives
a commuting wage adjustment is not
eligible for reclassification into another
area by the MCGRB. This adjustment is
exempt from certain budget neutrality
requirements. The thresholds and other
qualifying criteria for the commuting wage
adjustment are not subject to judicial
review. The provisions apply to discharges
on or after October 1, 2004.
Section 407. A hospital will not be able to
be denied treatment as a SCH or receive
payment as a SCH because data are
unavailable for any cost reporting period
due to changes in ownership, changes in
fiscal intermediaries, or other
extraordinary circumstances, so long as
data from at least one applicable base cost
reporting period is available. The provision
applies to cost reporting periods beginning
on or after January 1, 2004.
Permit hospitals with missing cost
reports to be SCHs. SCHs are hospitals
that, because of factors such as isolated
location, weather conditions, travel
conditions, or absence of other hospitals,
are the sole source of inpatient services
reasonably available in a geographic area,
or are located more than 35 road miles
from another hospital. An SCH receives
the higher of the following payment rates:
the current IPPS base payment rate, or its
hospital-specific per discharge costs from
either FY 1982, 1987 or 1996 updated to
the current year. The FY1996 base year
option will be fully implemented
beginning in FY2004.
Provide hospitals with data on patient
days for DSH adjustment. A hospital’s
DSH payments under IPPS are calculated
using a formula that includes data on the
Section 951. The Secretary is required to
provide information that hospitals need to
calculate the number of Medicaid patient
days used in the Medicare DSH payment
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
withdraws or elects to terminate its
payment. It would also be exempt from
certain budget neutrality requirements.
No provision.
Section 414. Beginning January 1, 2004,
a hospital would not be able to be denied
treatment as a SCH or receive payment as
a SCH because data are unavailable for any
cost reporting period due to changes in
o wn e r s h i p , c h a n g e s i n f i s c a l
intermediaries, or other extraordinary
circumstances, so long as data from at least
one applicable base cost reporting period is
available.
No provision.
Section 951. The Secretary would arrange
to furnish necessary patient day
information for the Medicare DSH
computation for the current cost reporting
CRS-17
Provision and Current Law Description
H.R. 1 as enacted
number of total patient days as well as
days provided to those eligible for
Medicaid and to Medicare beneficiaries
who receive Supplemental Security
Income.
Permit adoption of new coding standard.
The Secretary is required to rely on the
recommendations from the National
Committee on Vital and Health Statistics
(NCVHS) before adopting health
information standards and codes.
Require GAO report on use of external
data for IPPS payments. No provision in
current law.
formula not later than 1 year after
enactment.
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
year.
No provision.
No provision.
Section 942(c). GAO is required to study
which external data can be collected in a
shorter time frame by CMS to use in
calculating IPPS payments. GAO may
evaluate feasibility and appropriateness of
using quarterly samples or special surveys
and would include an analysis of whether
other executive agencies are best suited to
collect this information. The report is due
to Congress no later than October 1, 2004.
No provision.
Se c t io n 9 4 2 ( d) . T he new co d ing
standards, International Classification of
Diseases 10th Revision (IDC-10) could be
adopted within 1-year of enactment
without receiving a recommendation from
NCVHS.
Section 942(c). GAO would study which
external data can be collected in a shorter
time frame by CMS to use in calculating
IPPS payments. GAO could evaluate
feasibility and appropriateness of using
quarterly samples or special surveys and
would include an analysis of whether other
executive agencies are best suited to
collect this information. The report would
be due to Congress no later than October 1,
2004.
Critical Access Hospital Services
Increase payments to CAHs. Generally,
a critical access hospital (CAH) receives
reasonable cost reimbursement for care
rendered to Medicare beneficiaries. CAHs
may elect either a cost-based hospital
outpatient service reimbursement or an allinclusive rate which is equal to a
reasonable cost reimbursement for facility
services plus 115% of the fee schedule
payment for professional services.
Section 405(a). Inpatient, outpatient, and
covered skilled nursing facility services
provided by a CAH in its swing beds will
be reimbursed at 101% of reasonable costs
of services furnished to Medicare
beneficiaries. This provision applies to
cost reporting periods beginning on or
after January 1, 2004.
No provision.
Section 405(a). Inpatient, outpatient, and
covered skilled nursing facility services
provided by a CAH in its swing beds
would be reimbursed at 102% of
reasonable costs of services furnished to
Medicare beneficiaries. This provision
would apply to cost reporting periods
beginning on or after October 1, 2003.
CRS-18
Provision and Current Law Description
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Eliminate 35-mile requirement for costbased reimbursement of CAH
ambulance services. Ambulance services
provided by a CAH or provided by an
entity that is owned or operated by a CAH
are paid on a reasonable cost basis and not
the ambulance fee schedule, if the CAH or
entity is the only provider or supplier of
ambulance services that is located within a
35-mile drive of the CAH.
No provision.
Section 405(b). The requirement that the
CAH or the related entity be the only
ambulance provider within a 35-mile drive
in order to receive reasonable cost
reimbursement for the ambulance services
would be dropped for services furnished
beginning January 1, 2005.
Section 405(c). The 35-mile requirement
would not apply to a provider or supplier
of ambulance services who is a first
responder to emergencies for services
furnished after the first cost reporting
period beginning after the date of
enactment.
Expand payment for emergency room
on-call providers. BIPA required the
Secretary to include the costs of
compensation (and related costs) of on-call
emergency room physicians who are not
present on the premises of a CAH, are not
otherwise furnishing services, and are not
on-call at any other provider or facility
when determining the allowable,
reasonable cost of outpatient CAH
services.
Section 405(b). The provision expands
reimbursement of on-call emergency room
providers to include not just emergency
room physicians but also physician
assistants, nurse practitioners, and clinical
nurse specialists for the costs associated
with covered Medicare services provided
beginning January 1, 2005.
Section 405(c). Reimbursement for on-call
emergency room providers would be
expanded to include physician assistants,
nurse practitioners, and clinical nurse
specialists as well as emergency room
physicians for covered Medicare services
provided beginning January 1, 2005.
Section 405(b). Same provision but would
be effective January 1, 2004.
Increase critical access hospital (CAH)
bed limit. A CAH is a limited service
facility that
must provide 24-hour
emergency services and operate a limited
number of inpatient beds in which hospital
stays can average no more than 96 hours.
A CAH is limited to 15 acute-care beds,
but can have an additional 10 swing beds
that are set up for skilled nursing facility
level care. While all 25 beds in a CAH can
be used as swing beds, only 15 of the 25
can be used for acute care at any time.
Section 405(e). A CAH will be able to
operate up to 25 beds. The requirement
that only 15 of the 25 beds be used for
acute care at any time is dropped. The
provision applies to CAH designations
made before, on, or after January 1, 2004,
but any election made pursuant to the
regulations promulgated to implement this
provision will only apply prospectively.
Section 405(a) A CAH would be able to
operate up to 25 swing beds or acute care
beds, subject to the 96-hour average length
of stay for acute care patients. The
requirement that only 15 of the 25 beds be
used for acute care at any time would be
dropped.
This provision would be
effective for designations made beginning
October 1, 2004.
Section 405(f).
For designations
beginning January 1, 2004, the Secretary
would specify standards for establishing
seasonal variations in a CAH’s patient
admissions that would justify a five-bed
increase in the number of beds it can
maintain (and still retain its classification
as a CAH). CAHs with swing beds would
be able to use up to 25 beds for acute care
services as long as no more than 10 beds at
any time are used for non-acute services.
Those CAHs with swing beds that made
this election would not be eligible for the
CRS-19
Provision and Current Law Description
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
five-bed seasonal adjustment. A CAH
with swing beds that elects to operate 15 of
its 25 beds as acute care beds would be
eligible for the five-bed seasonal
adjustment.
Authorize periodic interim payments for
eligible CAHs. Eligible hospitals, skilled
nursing facilities, and hospices which meet
certain requirements receive Medicare
periodic interim payments (PIP) every 2
weeks; these payments are based on
estimated annual costs without regard to
the submission of individual claims. At
the end of the year, a settlement is made to
account for any difference between the
estimated PIP payment and the actual
amount owed. A CAH is not eligible for
PIP payments.
Section 405(c). An eligible CAH will be
able to receive payments made on a PIP
basis for its inpatient services. The
Secretary is required to develop alternative
methods for the timing of PIP payments to
these CAHs. This provision applies to
payments made on or after July 1, 2004.
Section 405(d). Starting with payments
made beginning January 1, 2005, an
eligible CAH would be able to receive
payments made on a PIP basis for inpatient
services.
Section 405(d). Same provision but would
be effective January 1, 2004. Also, the
Secretary would be required to develop
alternative methods based on the
expenditures of the hospital for these PIP
payments.
Exclude beds in distinct-part units from
CAH bed count Beds in distinct-part
skilled nursing facility units do not count
toward the CAH bed limit. Beds in
distinct-part psychiatric or rehabilitation
units operated by an entity seeking to
become a CAH count toward the bed limit.
Section 405(g). A CAH can establish a
distinct part psychiatric or rehabilitation
unit that meets the applicable requirements
for such beds. If the units do not meet
these requirements during a cost reporting
period, then no Medicare payment will be
made to the CAH for services furnished in
the unit during the period in question.
Payments for services provided in these
units will equal payments that are made on
a prospective payment basis to distinct part
units of short term general hospitals. The
beds in the distinct part psychiatric or
rehabilitation units will not count toward
the CAH bed limit. The total number of
beds in these distinct part units cannot
Section 405(g). The Secretary would not
be able to count any beds in a distinct-part
psychiatric or rehabilitation unit operated
by the entity seeking to become a CAH for
designations beginning October 1, 2003.
The total number of beds in these distinctpart units would not be able to exceed 25.
A CAH would be able to establish a such a
distinct-part unit.
No provision.
CRS-20
Provision and Current Law Description
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
exceed 10. The provision will apply to cost
reporting periods starting October 1, 2004
Establish CAH improvement
demonstration program. No provision in
current law.
No provision.
Section 415. The Secretary would be
required to establish a budget neutral 5year CAH demonstration program in four
areas including Kansas and Nebraska to
test various methods to improve the CAH
program. Services would be paid either on
the basis of its reasonable costs (without
regard to customary charges) or using the
relevant PPS for those services. In this
instance, reasonable cost reimbursement of
capital would include a return on equity
payment of 150% of the average rate of
interest paid by the Hospital Insurance (HI)
Trust Fund.
No provision.
Modify CAHs’ billing requirements for
physician services. As specified by
Balanced Budget Refinement Act of 1999
(BBRA), CAHs can elect to be paid for
outpatient services using cost-based
reimbursement for its facility fee and at
115% of the fee schedule for professional
services otherwise included within its
outpatient critical access hospital services
for cost reporting periods starting October
1, 2000.
Section 405(d). The requirement that all
physicians or practitioners providing
services in a CAH assign their billing
rights to the entity in order for the CAH to
be able to be paid 115% of the fee
schedule cannot be imposed. However, a
CAH will not receive payment based on
115% of the fee schedule for any
individual who does not assign billing
rights to the CAH. This provision applies
to cost report periods starting on or after
July 1, 2004 except for those CAHs that
have already elected payment for physician
services on this basis before November 1,
2003; this provision will apply to those
CAHs starting for cost reporting periods on
or after July 1, 2003.
No provision.
Section 405(e). The Secretary would not
be able to require that all physicians
providing services in a CAH assign their
billing rights to the entity in order for the
CAH to be able to be paid on the basis of
115% of the fee schedule for the
professional services provided by the
physicians. However, a CAH would not
receive such payment for any physician
who did not assign billing rights to the
CAH.
CRS-21
Provision and Current Law Description
H.R. 1 as enacted
S. 1 (as passed the Senate)
Eliminate state authority to waive CAH
mileage requirements. Currently, to
qualify as a CAH, the rural, for-profit,
nonprofit, or public hospital must be
located more than 35 miles from another
hospital or 15 miles in areas with
mountainous terrain or those where only
secondary roads are available. These
mileage standards may be waived if the
hospital has been designated by the State
as a necessary provider of health care.
Section 405(h). The State will no longer
be able to waive the mileage standards and
designate a facility seeking to become a
CAH as a necessary provider of care after
January 1, 2004. A facility designated as
CAH before January 1, 2006 and certified
as a necessary provider of care will be able
retain such designation.
No provision.
H.R. 1 (as passed the House)
No provision.
Other Hospitals
Create essential rural hospital category.
Generally, a hospital designated as a CAH
is exempt from IPPS and receives
reasonable, cost-based reimbursement for
care rendered to Medicare beneficiaries.
Certain acute general hospitals receive
special treatment under IPPS, particularly
those facilities identified as isolated or
essential hospitals primarily located in
rural areas, including RRCs and SCHs.
No provision.
No provision.
Section 403. The definition of CAH
hospital and services would be amended to
add an essential rural hospital. An eligible
hospital would apply for such a
classification, have more than 25 licensed
acute care beds, and be located in a rural
area as defined by IPPS. The Secretary
would have to determine that the closure of
this hospital would significantly diminish
the ability of beneficiaries to obtain
essential health care services based on
certain criteria. Such hospitals would not
be able to change such classification and
would not be able to be treated as a SCH,
Medicare dependent hospital or RRC
under IPPS and would be reimbursed
102% of its reasonable costs for inpatient
and outpatient services beginning October
1, 2004. Beneficiary cost-sharing amounts
would not be affected and required billing
for such services would not be waived.
CRS-22
Allied Health and Graduate Medical Education Payments.
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Pay hospitals for training costs of
psychologists. Medicare pays hospitals
for its share of direct costs associated with
approved hospital-based training programs
for nurses and certain other allied health
professionals including inhalation
therapists, nurse anesthetists, occupational
and physical therapists. Medicare does
not pay for such costs associated with
psychologists’ training.
No provision. Discussion of congressional
intent regarding this payment can be found
on p. 276 of the Conference Report
Section 408. Beginning October 1, 2004,
Medicare would reimburse its share of the
reasonable costs of approved education
activities of psychologists under the allied
health professional training provisions.
No provision.
Increase initial residency period for
geriatricians. Medicare counts residents
in their initial residency period (the lesser
of the minimum number of years required
for board eligibility in the physician’s
specialty or 5 years) as 1.0 FTE. Residents
whose training has extended beyond their
initial residency period count as 0.5 FTE.
Geriatrics is a subspecialty of family
practice, internal medicine and psychiatry.
A 1-year fellowship is required for
certification in geriatrics, following an
initial residency in one of those three areas.
Section 712. The bill clarifies that
Congress intended to provide an exception
to the initial residency period for geriatric
fellowship programs to accommodate
programs that require 2 years of training to
initially become board eligible in the
geriatric specialty. The Secretary is
required to promulgate interim final
regulations consistent with this expressed
intent after notice and subject to public
comment. The regulations will be effective
for cost reporting periods on or after
October 1, 2003.
Section 410. The Secretary would be
required to promulgate interim final
regulations after notice and comment that
would establish full GME payment for 2
years as a 2-year initial residency program
for certain geriatric training programs
effective for cost reporting periods
beginning October 1, 2003.
No provision.
Increase indirect medical education
(IME) payments.
A hospital’s IME
payment is based on a percentage add-on
to its IPPS rate that is established by a
complicated curvilinear formula that
currently provides a payment increase of
approximately 5.5% for each 10% increase
in the hospital’s intern and resident-to-bed
(IRB) ratio. The statutory formula is
multiplied by a hospital’s base payment
Section 502. From April 1, 2004 until
September 30, 2004, the IME multiplier is
equal to 1.47; during FY2005, the IME
multiplier is 1.42; during FY2006, the
IME multiplier is 1.37; during FY2007, the
IME multiplier is 1.32; and, starting
October 1, 2007, the IME multiplier is
equal to 1.35. This provision applies to
discharges on or after April 1, 2004.
Section 418. The IME multiplier in
FY2004 and in FY 2005 would be 1.36;
the multiplier would be 1.355 in FY2006
and in subsequent years. This would
provide an IME adjustment of 5.508% for
each 10% increase in a hospital’s IRB ratio
for FY2004 and FY2005. This change has
been projected to increase payments to
teaching hospitals by $300 million over 10
years.
No provision.
CRS-23
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
Section 713. For a 12-month period
starting January 1, 2004 hospitals will be
able to count residents in osteopathic and
allopathic family practice programs in
existence as of January 1, 2002 who are
training at non-hospital setting without
regard to the financial arrangement
between the hospital and the teaching
physician practicing in the non hospital
site. The Inspector General of Health And
Human Services (HHS-IG) will submit a
study including recommendations on the
appropriateness of the payment
methodology for the volunteer supervision.
Section 411. The Secretary would be
required to reimburse teaching hospitals
for residents in non-hospital locations,
when hospitals incur all, or substantially
all, the costs of the training in that site
starting from the effective date of a written
agreement between the hospital and the
entity owning or operating the non-hospital
site. The effective date of the written
agreement would be determined according
to generally accepted accounting
principles. The Secretary would not be
able to take into account the fact that the
hospital costs incurred are lower than
actual Medicare reimbursement. Starting
with FY2005, dental and podiatric
residents would be removed from the 3year rolling average calculation for IME
and DGME reimbursements.
H.R. 1 (as passed the House)
rate for each Medicare discharge to
determine the IME payments: 1.35 X [(1+
IRB)0.405 - 1]. The multiplier of 1.35
increases the level of the IME adjustment
to the existing target level of 5.5%.
Congress has periodically changed the
multiplier to decrease or increase IME
payments to teaching hospitals.
Count residents in a non-provider
setting; drop dentists and podiatrists
from the 3-year rolling limit on IME
payments. Medicare has different resident
limits for the IME adjustment and direct
medical education (DGME) payment.
Generally, the resident counts for both
IME and DGME payments are based on
the number of residents in approved
allopathic and osteopathic teaching
programs reported by the hospital in
calendar year 1996. The DGME limit may
differ from the IME limit because in 1996
residents training in non-hospital sites were
eligible for DGME payments but not for
IME payments. Prior to BBA 1997, the
number of residents that could be counted
for IME purposes included only those in
the hospital inpatient and outpatient
departments. Effective October 1, 1997,
under certain circumstances, a hospital
may now count residents in non-hospital
sites for the purposes of IME. Subject to
these resident limits, a teaching hospital’s
IME and DGME payments are based on a
3-year rolling average of resident counts.
The rolling average calculation includes
No provision.
CRS-24
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
podiatry and dental residents. CMS has
proposed regulations that limit Medicare’s
medical education payments when existing
residents are transferred from a nonhospital entity to a teaching hospital,
particularly when the non-hospital entity
has historically paid for the training costs
without hospital funding.
Extend update limitation on high cost
programs. Hospitals with per resident
amounts between 85% and 140% of the
geographically-adjusted national average
would continue to receive payments based
on their hospital-specific per resident
amounts updated for inflation.
Section 711. Hospitals with per resident
amounts above 140% of the geographically
adjusted national average amount will not
get an update from FY2004 through
FY2013.
No provision.
Section 711. Hospitals with per resident
a mo u n t s a b o v e 1 4 0 % o f t h e
geographically-adjusted national average
amount would not get an update from
FY2004 through FY2013.
Redistribute unused residency positions.
Medicare has different resident limits for
the IME adjustment and DGME payment.
Generally, the resident counts for both
IME and DGME payments are based on
the number of residents in approved
allopathic and osteopathic teaching
programs that were reported by the
hospital for the cost reporting period
ending in calendar year 1996. The DGME
resident limit is based on the unweighted
resident counts. It may differ from the
IME limit because in 1996 residents
training in non-hospital sites were eligible
for DGME payments but not for IME
payments. Generally, a hospital’s IME
adjustment and increased IPPS payments
depends on a hospital’s teaching intensity
as measured by the ratio of the number of
Section 422. A teaching hospital’s total
number of resident positions will be
reduced for cost reporting periods starting
July 1, 2005 if its reference resident level
is less than its applicable resident limit.
Rural hospitals with less than 250 acute
care inpatient beds would be exempt from
these reductions. The reduction for other
hospitals will equal 75% of the difference
between the hospital’s limit and its
reference resident level. The reference
resident level is the highest number of
allopathic and osteopathic resident
positions (before the application of any
weighting factors) for the hospital during
the reference period. This reference period
is either (1) the resident level of the most
recent cost reporting period of the hospital
for which a cost report has been settled (or
No provision.
Section 406. A teaching hospital’s total
number of Medicare-reimbursed resident
positions would be reduced by a portion of
its unused residency slots for cost reporting
periods starting January 1, 2004 if its
resident reference level is less than its
applicable resident limit. If so, the
reduction would be equal to 75% of the
difference between the hospital’s limit and
its resident reference level upon the timely
request for such an adjustment, for the cost
reporting period that includes July 1, 2003.
A hospital’s reference period would be the
three most recent settled or submitted
consecutive cost reporting periods on or
before September 30, 2002. The need for
an increase in the physician specialty and
the location involved would be considered.
Positions would be distributed to programs
CRS-25
Provision and Current Law
H.R. 1 as enacted
interns and residents per bed. Medicare’s
DGME payment to teaching hospitals is
based on its updated cost per resident
(subject to a locality adjustment and
certain payment corridors), the weighted
number of approved full-time equivalent
(FTE) residents, and Medicare’s share of
inpatient days in the hospital.
submitted, subject to audit) on or before
September 30, 2002 or (2) the resident
level for the cost reporting period that
includes July 1, 2003 subject to audit. A
hospital’s reference level may be adjusted
under certain circumstances. The increase
in applicable resident limits applies to
portions of cost reporting periods
occurring on or after July 1, 2005. The
aggregate increase may not exceed the
overall reduction in such limits. The
Secretary is directed to take several factors
into account when distributing the resident
positions to hospitals. No more than 25
additional FTEs will be given to any
hospital. These hospitals will be
reimbursed for DGME for the increase in
resident positions at the locality adjusted
national average per resident amount and
will receive increased IME payments as
well for discharges after July 1, 2005.
The Secretary is required to submit a
report to Congress no later than July 1,
2005 on whether to extend the application
deadline for increases in resident limits.
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
in rural areas and those not in large urban
areas on a first-come-first-served basis.
The hospital would have to demonstrate
that the resident positions would be filled;
not more than 25 positions would be given
to any hospital. These hospitals would be
reimbursed for DGME for the increase in
resident positions at the locality-adjusted
national average per resident amount. IME
payments would also be affected. The
Secretary would be required to submit a
report to Congress, no later than July 1,
2005, on whether to extend the application
deadline for increases in resident limits.
Skilled Nursing Facility (SNF) and Hospice Services.
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Skilled Nursing Facility Services (SNF)
Increase skilled nursing facility (SNF)
payments for AIDS patients. Under PPS,
SNFs are paid a daily rate that varies
depending on the care needs of the
Section 511. Starting October 1, 2004, the
per diem RUG payment for a SNF resident
with acquired immune deficiency
syndrome (AIDS) will be increased by
No provision.
Section 511. Starting October 1, 2003, the
per diem RUG payment for a SNF resident
with acquired immune deficiency
syndrome (AIDS) would be increased by
CRS-26
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
beneficiary. There are 44 resource
utilization groups (RUGs) used to adjust
payment for care needs; each group
reflects the intensity of services, such as
skilled nursing care and/or various therapy
and other services needed by a beneficiary.
128%. This increase does not apply after
the date that the Secretary certifies that the
case-mix adj ustment adequately
compensates for the increased costs
associated with caring for residents with
AIDS.
Exclude certain clinic visits from skilled
nursing facility (SNF) prospective
payment system (PPS) Under Medicare’s
PPS, SNFs are paid a predetermined
amount to cover all services provided in a
day adjusted for the care needs of the
patient. Certain services and items
provided a SNF resident, such as
physicians’ services, specified ambulance
services, specified chemotherapy items and
services, and certain outpatient services
provided by a Medicare-participating
hospital or CAH, are excluded from the
SNF-PPS and paid separately under Part B.
Section 410. Services provided to a SNF
resident by a rural health clinic (RHC) and
a federally qualified health center (FQHC)
after January 1, 2005 are excluded from
SNF-PPS if these services would have
been excluded if furnished by a physician
or practitioner who was not affiliated with
a RHC or FQHC.
Section 429. Services provided by a RHC
and a FQHC after January 1, 2005 would
be excluded from SNF-PPS if these
services would have been excluded if
furnished by a physician or practitioner
who was not affiliated with a RHC or
FQHC.
Outpatient services that are
beyond the general scope of SNF
comprehensive care plans that are provided
by an entity that is 100% owned as a joint
venture by two Medicare-participating
hospitals or critical access hospitals would
be excluded from the SNF-PPS.
Section 408. Provision is limited to RHCs
and FQHC services provided after January
1, 2004 and does not extend to outpatient
services that are beyond the general scope
of SNF comprehensive care plans.
Require background check on workers
for certain Medicare and Medicaid
health and long-term care providers.
Nursing homes and home health agencies
may request the Federal Bureau of
Investigation (FBI) to search its all-state
national data bank of arrest and
convictions for the criminal histories of
applicants who would provide direct
patient care, as long as states establish
mechanisms for processing these requests
(most states require checks for certain
groups of employees). Providers follow
certain procedures to conduct these checks.
Section 306. The Secretary, in consultation
with the Attorney General, is required to
establish pilot projects on background
checks for certain long-term care workers
with direct access to patients or residents in
no more than 10 states. The Secretary is
required to establish criteria for selecting
those states that volunteer to participate.
The bill specifies procedures for
conducting background checks, and
includes searches of state and FBI criminal
records. At least one state in the pilot
project would be allowed to establish
procedures for using employment agencies
Section 636. All providers of long-term
care services that participate in Medicare
and/or Medicaid would be required to
initiate background checks for certain
workers with access to a patient or
resident. Procedures for conducting
background checks would be specified,
and would include searches of state and
FBI criminal records. Violators of these
requirements would be subject to criminal
penalty fines and/or imprisonment.
Providers would be permitted to
provisionally employ workers pending
completion of the checks and would be
No provision.
128%. This increase would not apply after
the date that the Secretary certifies that the
case-mix adj ustment adequately
compensates for the increased costs
associated with caring for residents with
AIDS.
CRS-27
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
HHS maintains a national health care
fraud and abuse data base, the Healthcare
Integrity and Protection Data Bank
(HIPDB). Self-queries of HIPDB are
allowed by government agencies, health
plans, health care providers, suppliers and
practitioners. All states also maintain their
own registries of those persons that the
state determines meet the requirements to
work as nurse aides. Included in these
registries are data describing state findings
of resident neglect, abuse and/or the
misappropriation of resident property.
to conduct these checks. Providers may
provisionally employ workers pending
completion of the checks.
reimbursed for their costs of conducting
these checks.
The Secretary is required to pay those
states for the costs of conducting the pilot
program (reserving 4% of the payments for
the program’s evaluation). A sum of $25
million is appropriated from funds in the
Treasury not otherwise appropriated, for
fiscal years 2004 through 2007.
H.R. 1 (as passed the House)
The nurse aide registry would be expanded
to include all employees of long-term care
providers and renamed “employee
registry.” The investigatory responsibilities
of survey and certification agencies would
be expanded. $10.2 million would be
authorized to be appropriated for FY 2004,
with compliance deadlines varying by
provider group.
Grants would be available to develop
information on best practices in patient
abuse prevention training and for other
purposes.
State survey agencies are required to
investigate allegations of resident neglect,
abuse and/or the misappropriation of
resident property in nursing homes.
Long-term care providers could access the
HIPDB data bank and more information
would be required to be included. A report
on background checks would be due to
Congress no later than 2 years after
enactment.
Hospice Services
Permit hospices to provide core hospice
services under arrangement. Medicare
requires a hospice to provide certain core
services directly. These core services
include nursing care, medical social
services, and counseling services.
Section 946. Beginning with the date of
enactment, a hospice is permitted to enter
into arrangements with another hospice
program to provide core services in
extraordinary circumstances.
Section 406. Beginning with the date of
enactment, a hospice would be permitted
to enter into arrangements with another
hospice program to provide core service in
extraordinary circumstances.
Section 946. Same provision.
CRS-28
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Permit nurse practitioners, clinical
nurse specialists, and physician
assistants to attend hospice patients.
Medicare covers hospice services to care
for the terminal illness of a beneficiary.
Reasonable and necessary medical and
support services for the management of the
terminal illness are furnished under a
written plan-of-care established and
periodically reviewed by the patient’s
attending physician and the hospice. The
attending physician may be employed by
the hospice and is identified by the
beneficiary as having the most significant
role in the determination and delivery of
medical care to the beneficiary at the time
that hospice care is elected.
Section 408. The definition of an attending
physician in hospice is expanded to include
a nurse practitioner. A nurse practitioner is
not permitted to certify a beneficiary as
terminally ill for the purposes of receiving
the hospice benefit. The provision is
effective upon enactment.
Section 407. Beginning October 1, 2004,
a terminally ill beneficiary under hospice
care would be able to designate a physician
assistant, nurse practitioner, or clinical
nurse specialist (who is not an employee of
the hospice program) as his or her
attending physician. The written plan-ofcare would be able to be established by
these professionals who would be able to
periodically review the beneficiary’s
written plan-of-care.
Section 409. Nurse practitioners would be
permitted to be identified as a beneficiary’s
attending physician and would be able to
establish and review the written plan-ofcare as well as provide other services, but
would not be able to certify that a
beneficiary is terminally ill.
Pay for physician consultation services
in certain instances.
Current law
authorizes coverage of hospice services, in
lieu of certain other Medicare benefits, for
terminally ill beneficiaries who elect such
coverage. The hospice can be paid by
Medicare only after the beneficiary has
elected the hospice benefit
Section 512. Beginning January 1, 2005,
Medicare will pay for a hospice-employed
physician’s consultation with a terminally
ill beneficiary who has not elected the
hospice benefit.
No provision.
Section 512. As of January 1, 2004,
Medicare would pay for a hospiceemployed physician’s consultation with a
terminally ill beneficiary who has not
elected the hospice benefit.
Establish rural hospice demonstration
program. Medicare’s hospice services
are provided primarily in a patient’s home
to beneficiaries who are terminally ill and
who elect such services. Medicare law
prescribes that the aggregate number of
days of inpatient care provided to
Medicare beneficiaries who elect hospice
care in any 12-month period cannot
Section 409. The Secretary is required to
establish a demonstration project in 3
hospice programs to deliver hospice care to
Medicare beneficiaries in rural areas. A
project is not permitted to last longer than
5 years. Those Medicare beneficiaries who
lack an appropriate caregiver and are
unable to receive home-based hospice care
could receive hospice care in a facility of
No provision.
Section 418.
The Secretary would
establish a 5-year demonstration project in
three hospice programs to deliver hospice
care to Medicare beneficiaries in rural
areas. Those Medicare beneficiaries who
lack an appropriate caregiver and are
unable to receive home-based hospice care
would be able to receive hospice care in a
facility of 20 or fewer beds that offers a
CRS-29
Provision and Current Law
H.R. 1 as enacted
exceed 20% of the total number of days of
hospice coverage provided to these
persons.
20 or fewer beds that offers a full range of
hospice services within its walls.
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
full range of hospice services within its
walls. The facility would not be required
to offer services outside of the home and
the limit on the aggregate number of
inpatient days provided to Medicare
beneficiaries who elect hospice care would
be waived.
Other Part A Provisions.
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Make grants to States and certain
rural hospitals. The Secretary is able to
make grants for specified purposes to
States or eligible small rural hospitals
that apply for such awards under the
Medicare Hospital Flexibility Program.
The Secretary may also award grants to
hospitals to assist eligible small rural
hospitals (with less than 50 beds) in
implementing data systems required
under BBA 1997. Annual funding for the
Rural Hospital Flexibility Grant Program
was $25 million from 1999 through
2001; $40 million in FY2002; and $25
million in 2003. The authorization to
award the grants expired in FY2002.
Section 405(f). The rural hospital
flexibility grant program is authorized at
$35 million each year from FY2005
through FY2008. Starting in FY2005, a
state is required to consult with the hospital
association and rural hospitals in the state
on the most appropriate way to use such
funds. A state may not spend more than
the lesser of 15% of the grant amount or
the States’ federally negotiated indirect
rate for administrative purposes.
Beginning with FY2005, up to 5% of the
total amount appropriated for grants will
be available to the Health Resources and
Services Administration for administering
these grants.
Section 405(f). Under this program, the
Secretary would be able to award grants of
up to $50,000 to hospitals to assist eligible
small rural hospitals in reducing medical
errors and increasing patient safety under
the new Small Rural Hospital
Improvement Program. Appropriations of
$25 million each year from the Treasury
from FY2004 through FY2008 would be
authorized for this purpose.
Appropriations of $40 million each year
from FY2004 through FY2008 from the HI
Trust Fund for grants to states for specified
purposes would be authorized. States that
are awarded grants would be required to
consult with the hospital associations and
rural hospitals in the state.
Section 405(g). The authorization to
award grants under the existing Rural
Hospital Flexibility Program would be
established from FY2004 through FY2008
from the Federal HI Trust Fund at amounts
of up $25 million each year.
Establish health care infrastructure loan
program. No provision in current law.
Section 1016. A loan program will be
established to improve the cancer-related
health care infrastructure. In order to
receive assistance, the applicant will be
required to: (1) be engaged in cancer
research; and (2) be designated as a
Section 608. A loan program would be
established to improve the cancer-related
health care infrastructure in states with a
population of less than 3 million. In order
to receive assistance, the applicant would
be required to: (1) be engaged in cancer
No provision.
CRS-30
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
cancer center for the National Cancer
Institute (NCI) or be similarly designated
by the state. $200 million in budget
authority is authorized for July 1, 2004
through FY2008 to carry out the loan
program, $2 million for program
administration. By 4 years from enactment,
the Secretary will submit a report to
Congress on continuing the program.
research; and (2) be designated as a cancer
center for the NCI or be similarly
designated by the state. $49 million in
budget authority would be authorized for
July 1, 2004 through FY2008 to carry out
the loan program, $2 million for program
administration.
Establish capital infrastructure
revolving loan program The Public
Health Services Act establishes a fund in
the Treasury from which the Secretary of
HHS can make loans or loan guarantees in
the amounts that have been specified in
appropriations acts from time to time.
Under the Medicare Rural Hospital
Flexibility Program established as part of
Title XVIII, the Secretary may award
grants to rural hospitals to cover the
implementation costs associated with data
systems needed to meet the BBA 97
requirements.
No provision.
Section 609. The Secretary would be able
to make loans to any rural entity including
rural health clinics, a medical facility with
less than 50 beds in non- MSA counties or
in rural census tracts of MSAs, rural
referral centers or sole community
hospitals for various purposes. An
geographically reclassified entity would be
eligible for these loans and loan
guarantees.
The government’s total
exposure for this program would not
exceed $50 million per year and the
principal amount of all loans directly made
or guaranteed in any year is not to exceed
$250 million per year. In addition, rural
providers could apply to receive $50,000
planning grants to help assess capital and
infrastructure needs. The grants awarded
in any year would not exceed $2.5 million.
The program would expire after September
30, 2008.
No provision.
Establish rural community hospital
demonstration program. No provision
in current law.
Section 410A. The Secretary will establish
a 5-year rural community hospital (RCH)
demonstration program in selected rural
areas with low population densities. Under
Section 414. The Secretary would be
required to establish a 5-year RCH
demonstration program in 4 areas
including Kansas and Nebraska to pay for
No provision.
CRS-31
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
the program, up to 15 hospitals with 50
acute care beds will receive payment for
inpatient services either on the basis of its
reasonable costs (without regard to the
amount of customary charges) or using a
target amount.
The project will be
implemented not later than January 1, 2005
and not before October 1, 2004. The
project would be budget neutral. Certain
limits on beneficiary cost-sharing will be
imposed. The Secretary will submit a
report with recommendations to Congress
no later than 6 months after completion of
the project
acute inpatient services, outpatient
services, and certain home health services
in qualifying hospitals either on the basis
of its reasonable costs (without regard to
the amount of customary charges) or using
the respective prospective payment
systems for those services. In this instance,
reasonable cost reimbursement of capital
costs would include a return on equity
payment of 150% of the average rate of
interest paid by the HI Trust Fund. The
project would be budget neutral. Certain
limits on beneficiary cost-sharing would be
imposed.
Ensure status as long-term hospitals
for certain hospital-in-hospitals. A
hospital-in-a-hospital is a long-term care
hospital that is physically located in an
acute care hospital. CMS has established
certain requirements for these entities to
be excluded from the IPPS and be paid as
a long-term hospital. It exempted
existing entities (those that were in
existence on or before September 30,
1995) when these requirements were
established. On May 19, 2003, CMS
proposed that a grandfathered hospitalin-a hospital would only be exempt from
the existing requirements if it continues
to operate within the same terms and
conditions that were in effect as of
September 30, 1995.
No provision.
Section 416. The Secretary would not be
able to impose any special conditions on
the operation, size, number of beds, or
location of an existing long-term hospital
in order to continue participating in
Medicare or Medicaid or to continue being
classified as a long-term hospital. The
Secretary would not be able to adopt a
proposed regulation that would implement
such conditions or any revision to such
regulation that have a comparable effect.
[Duplicate provision is at Section 420B]
No provision.
Establish special treatment for certain
entities. Unlike other providers, acute
hospitals may apply to the Medicare
Section 508(f). Reclassifications of a
county or area made by an Act of Congress
that expired on September 30, 2003 shall
Section 417. Starting October 1, 2003,
Iredell County and Rowan County, North
Carolina would be deemed to be located in
No provision.
CRS-32
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
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. Hospital
reclassifications are established on a
budget neutral basis so aggregate inpatient
prospective payment system expenditures
will not increase as a result. Aside from
reclassifications through the MGCRB,
hospitals have also been reclassified by
law.
be reinstated starting on January 1, 2004
through September 30, 2004.
Limit charges for contract health
services provided to Indians by
participating hospitals.
The Indian
Health Service (IHS) provides health care
both directly, through tribes and tribal
consortia, and through urban Indian
organizations.
Section 506. Hospitals that participate in
Medicare and that provide Medicare
covered inpatient hospital services under
the contract health services program
funded by the Indian Health Services and
operated by the Indian Health Service, an
Indian tribe, an Indian tribal organization,
or an urban Indian organization will be
paid in accordance with regulations
promulgated by the Secretary regarding
admission practices, payment
methodologies, and rates of payments.
This will include the requirement to accept
these rates as payment in full except for the
payment rates for neonatal care. This
provision will apply to Medicare
participation agreements in effect or
entered into by a date specified by the
Secretary. In no case will this date be later
than 1 year after the date of enactment.
the Charlotte-Gastonia-Rock Hill, NC-SC
Metropolitan Statistical Area for the
purpose of Medicare’s inpatient and
outpatient acute hospital payments as well
as SNF and home health payments. The
Secretary would be required to adjust the
wage index values of all hospitals in North
Carolina to assure that aggregate payments
for hospital inpatient operating costs are
not greater than they would have been
without such a change: also aggregate
payments for SNF and home health
services in North Carolina would not be
greater than they would have been without
such a change.
Section 412. The amendment would
prohibit Medicare providers from charging
the Indian Health Service more than the
Medicare-established rates for inpatient
hospital services.
H.R. 1 (as passed the House)
No provision.
CRS-33
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
Pay interest on clerical error into HI
Trust Fund. An incorrect amount of
income was transferred into the HI Trust
Fund in April 2001, because of a clerical
error.
An additional amount was
transferred into the HI Trust Fund in
December, 2001 to correct for the principal
amount associated with the error.
Correction of the interest associated with
the clerical error requires legislation.
Section 734. The Secretary of the Treasury
is required to transfer into the HI Trust
Fund an amount that would have been held
by that fund if the clerical error had not
occurred. The appropriation is to be made
and transfer is required within 120 days of
enactment of this Act. In the case of a
clerical error that occurs after April 15,
2001, the Secretary of the Treasury is
required to notify the appropriate
committees of Congress about the error
and the actions to be taken, before such
action is taken.
Section 947. Public hospitals, not
otherwise subject to the Occupational
Safety and Health Act of 1970, are
required to comply with the Bloodborne
Pathogens standard under section
1910.1030 of title 29 of the Code of
Federal Regulations. A hospital that fails
to comply with the requirement will be
subject to a civil monetary penalty, but
cannot be terminated from participating in
Medicare.
The provision applies to
hospitals as of July 1, 2004.
Section 623. After consultation with the
Secretary of HHS, the Secretary of the
Treasury would be required to transfer into
the HI Trust fund an amount that would
have been held by that fund if the clerical
error had not occurred within 120 days of
enactment.
Section 513. Same provision.
No provision.
Section 947. As of July 1, 2004, public
hospitals that are not otherwise subject to
OSHA would be required to comply with
the Bloodborne Pathogens standard under
Section 1910.1030 of Title 29 of the Code
of Federal Regulations. A hospital that
fails to comply with the requirement would
be subject to a civil monetary penalty, but
would not be terminated from participating
in Medicare.
Apply the Occupational Safety and
Health Act of 1970 (OSHA) bloodborne
pathogens standard to public hospitals.
Section 1866 of the Social Security Act
establishes certain conditions of
participation that hospitals must meet in
order to participate in Medicare.
H.R. 1 (as passed the House)
CRS-34
Provisions Relating to Part B
Physician and Practitioner Services.
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Establish floor on geographic
adjustment for physician fee schedule.
Medicare’s payment for physicians’
services under a fee schedule has three
components: the relative value for the
service, geographic adjustment factors and
a conversion factor into a dollar amount.
The geographic adjustment factors are
indices that reflect the relative cost
difference in a given area in comparison to
the national average
Section 412. The Secretary is required to
increase the value of any work geographic
index that is below 1.0 to 1.0 for services
furnished on or after January 1, 2004 and
before January 1, 2007
Section 421. For services furnished after
January 1, 2004, the Secretary would be
required to increase the value of any work
geographic index that is below .980 to
.980. The values for work index would be
raised to 1.0 for services furnished in 2005,
2006, and 2007. The practice expense and
malpractice geographic indices in low
value localities areas would be raised to
1.00 for services furnished in 2005 until
2008.
Section 605(a). For services furnished
after January 1, 2004 and before January 1,
2006, the Secretary would be required to
increase the value of any work geographic
index that is below 1.00. to 1.00 unless the
Secretary determines, based on the
subsequent GAO study which is due by
September 1, 2004, that there is no sound
economic rationale for such change.
Increase practice expense payments for
certain specialists. The relative value
associated with a particular physician
service is the sum of three components one
of which is practice expense. Practice
expense includes both direct costs (such as
a clinician’s time and the medical supplies
to provide a specific service to a patient)
and indirect costs (such as rent and
utilities). BBRA required the Secretary to
establish a data collection process and
standards for determining practice expense
relative values as well as to use data
collected or developed outside HHS, to the
maximum extent practicable, consistent
with sound data collection practices. The
relative values are periodically reviewed
and adjusted to account for various factors;
changes that cause more than $20 million
in spending trigger a budget neutrality
adjustment.
Sections 303(a) and 304. Beginning in
2004, the practice expense relative value
units for oncology administration services
will be adjusted using survey data that was
collected as of January 1, 2003 (this data
was submitted by the American Society of
Clinical Oncologists); the additional
expenditures will be exempt from the
budget neutrality requirement in 2004. The
work relative value units for drug
administration services furnished on or
after January 1, 2004 will be equal to the
work relative value units for a level 1
office medical visit for an established
patient. Starting in 2005 through 2006, the
practice expense relative values for other
drug administration services will be
increased in the physician fee schedule
using appropriate supplemental survey data
submitted by March 1, 2004, for 2005, or
March 1, 2005 for 2006. Data will be
Section 432(b)(1). The Secretary would
establish the practice expense relative
values for the CY2004 fee schedule using
the survey data from a physician specialty
group as of January 1, 2003 if the data
appropriately covers the practice expenses
for oncology administration services. The
Secretary would review and appropriately
modify payments for the administration of
more than one anti-cancer agent to a
patient in a day. The resulting increase in
spending would be exempt from the
budget neutrality requirement. Also, the
Secretary would change the non-physician
work pool method so that associated
payments are not inordinately reduced.
These adjustments would not be
implemented unless other outpatient drug
pricing changes in the section are
implemented.
Section 303(a) The Secretary would
increase the practice expense relative
values for the physician fee schedule in
CY2005 using appropriate survey data on
the expenses associated with drug
administration provided by entities and
organizations that are submitted by
December 31, 2004. Using existing
processes for coding considerations, the
Secretary would evaluate existing codes
for drug administration to ensure accurate
reporting and billing for these services.
Any resulting CY2005 payment increase
would not be subject to budget neutrality
provisions, would be exempt from
administrative and judicial review, and
would be treated as a change in law and
regulation in the sustainable growth rate
determination.
Subsequent budget
neutrality adjustments would be permitted.
The same non-physician work pool
CRS-35
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
methodology provision as in S. 1 is
included.
accepted from those specialists who
received 40% or more of their Medicare
payments in 2002 from drugs and
b iologicals. The existing d r ug
administration codes will be evaluated
under existing processes after consultation
with interested parties. These adjustments
in practice expense relative value units for
certain drug administration services are
exempt from the budget neutrality
requirements in 2005, 2006, and 2007.
The Secretary can adjust practice expense
payments in subsequent years, subject to
the budget neutrality provisions. The
effect of the nonphysician workpool
methodology will not be changed.
Medicare’s payment policy in effect on
October 1, 2003, for the administration of
more than one drug or biological to an
individual on a single day through the push
technique will be modified and the
increased payments will be exempt from
the budget-neutrality requirement in 2004.
A transitional adjustment (or additional
payment) of 32% in 2004 and 3% in 2005
will be made.
Increase payments to physicians in
newly created scarcity areas; change
Medicare Incentive Program (MIP).
Physicians providing services in a health
professional shortage area (HPSA) are
entitled to an incentive payment from the
Medicare program.
This incentive
payment is a 10% increase over the
amount which would otherwise be paid
under the physician fee schedule.
Section 413. Certain physicians, both
primary care and specialists, in scarcity
areas are eligible for an additional 5%
increase in payments starting on January 1,
2005 and ending by January 1, 2008. To
determine the scarcity areas, the Secretary
will calculate ratios of practicing primary
care physicians and specialists to Medicare
beneficiaries, rank each county (or
equivalent area) according to each ratio,
H.R. 1 (as passed the House)
Section 422. The Secretary would be
required to establish procedures to
determine when a physician in a HPSA is
eligible for a bonus payment.
The
Secretary would also be required to
establish an ongoing education program,
an ongoing study and submit annual
reports. A GAO report would be required
no later than 1 year from enactment.
Section 417. Same provision with respect
to Secretary developing procedures to
identify physicians eligible for bonus
payments. Also, physicians in newlycreated scarcity areas as well as other
physicians would be eligible for an
additional 5% increase in their fee
schedule payment amounts. The Secretary
would also be required to publish a list of
all areas that qualify as a HPSA each year
CRS-36
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
in the proposed and final rule
implementing the physician fee schedule.
and then identify those areas with the
lowest ratios which collectively represent
20% of the total Medicare beneficiary
population in those areas. The list of
counties will be revised no less often than
once every 3 years unless there are no new
data. There will be no administrative or
judicial review of the designation of the
county or area as a scarcity area, the
designation of an individual physician’s
specialty, or the assignment of a postal zip
code to the county or other area. MIP
payments to physicians in HPSAs that
consist of entire counties will be made
without requiring the physician to identify
the HPSA when requesting payment.
Revise reassignment provisions.
Beneficiaries are the parties who are
entitled to receive Medicare payments
under the Medicare statute. However, most
beneficiaries assign these rights to
participating physicians, suppliers, and
other providers who directly provide the
care and then submit claims for Medicare
payment. Although Medicare permits
physicians to reassign their right to
payment to certain other entities, they
cannot reassign their right to payment to
staffing companies (entities that retain
physicians on a contractual basis).
Section 952. The bill permits Medicare
payment for Part B services to be made to
an entity, as defined by the Secretary, that
has a contractual arrangement with the
physician or other person who provided
the service. In order to bill for the service,
the entity and the contractual arrangement
will have to meet program integrity and
other safeguards specified by the
Secretary.
Section 434.
Staffing companies
(individuals or entities) would be able to
submit claims to Medicare for physician
services provided under contractual
arrangement between the company and the
physician, if the arrangement meets
appropriate program integrity and other
safeguards established by the Secretary.
Section 952. Same provision with some
drafting differences.
Extend provision for separate payments
of certain inpatient pathology services.
In general, independent laboratories cannot
directly bill for the technical component of
pathology services provided to Medicare
Section 732. Direct payments for the
technical component for these pathology
services will be made for services
furnished during 2005 and 2006.
Section 435. Direct payments for the
technical component for these pathology
services would be made for services
furnished during 2005.
Section 734. Similar provision except
Medicare would make direct payments for
the technical component of pathology
services from 2004 though 2008. Would
also specify that a change in hospital
CRS-37
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
ownership would not affect these direct
billing arrangements.
beneficiaries who are inpatients or
outpatients of acute care hospitals. BIPA
permitted certain independent laboratories
with existing arrangements with acute
hospitals to do so if the arrangement had
been in effect as of July 22, 1999. The
direct payments for these services apply to
services furnished during a 2-year period
starting on January 1, 2001 and ending
December 31, 2002.
Increase Medicare payments to
physicians in Alaska. Physicians that
provide services to Medicare beneficiaries
are paid based on Medicare’s physician fee
schedule that is adjusted to account for
geographic variations in practice expenses.
Section 602. Physicians in Alaska with
values of practice expense, malpractice,
and work geographic index below 1.67
will have these values raised to 1.67
starting January 1, 2004 and before
January 1, 2006.
Section 450K. For 2004, physicians in
Alaska would be paid 90% of the VA
physician fee schedule used for FY2001.
In 2005, this amount would be increased
by the update amount for the Medicare
physician fee schedule for 2005. If no VA
fee schedule amount exists for a service,
the payment amount would be an
adjustment to the Medicare payment. The
adjustment would equal 90% of the overall
percentage difference between the two fee
schedules weighted by the distribution of
Medicare claims in 2001.
No provision.
Establish update to physician fee
schedule. Medicare pays for services of
physicians and certain non-physician
practitioners on the basis of a fee schedule.
The law provides a specific formula for
calculating the annual update to the
conversion factor.
Section 601. The update to the conversion
factor for 2004 and 2005 will not be less
than 1.5% and will be exempt from the
budget neutrality adjustment.
No provision.
Section 601. The update to the conversion
factor for 2004 and 2005 would be not less
than 1.5% and would be exempt from the
budget neutrality adjustment.
CRS-38
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Change the sustainable growth rate
formula. Medicare pays for services of
physicians and certain non-physician
practitioners on the basis of a fee schedule.
The law provides a specific formula for
calculating the annual update to the
conversion factor which regulates overall
spending for physicians’ services. Several
factors enter into the calculation of the
formula. One of those factors is the
sustainable growth rate (SGR) which is
essentially a target for Medicare spending
growth in physicians’ services. One
measure used to calculate the SGR is the
annual percentage change in gross
domestic product (GDP). If expenditures
exceed the target, the update for a future
year is reduced. If expenditures are less
than the target, the update is increased.
The recent negative update adjustment
factors reflect the application of the SGR
system.
Section 601. The formula for calculating
the sustainable growth rate will be
modified. Starting in 2003, the GDP factor
will be based on the annual average change
over the preceding 10 years (a 10-year
rolling average). The 10-year rolling
average calculation of the GDP will apply
to computations of the SGR starting in
2003.
Section 464. The provision expresses a
sense of the Senate that Medicare
beneficiary access to quality care may be
compromised if Congress does not prevent
cuts in 2004 and following years that stem
from the SGR formula. [Duplicate of
Section 622]
Section 601. The formula for calculating
the sustainable growth rate would be
modified. Starting with the SGR for 2003,
the GDP factor would be based on the
annual average change over the preceding
10 years (a 10-year rolling average). This
calculation would replace the current GDP
factor which measures the 1-year change
from the preceding year.
Require GAO report on physician
compensation. No provision in current
law.
No provision.
Section 629. The provision provides a
sense of the Senate that the reductions in
Medicare’s physician fee schedule are
destabilizing, primarily caused by the
sustainable growth rate calculation, and
that CMS should use its discretion to make
certain exclusions and adjustments to the
SGR calculation.
No provision.
Section 953(a). No later than six months
from enactment, GAO would report to
Congress on the appropriateness of the
conversion factor updates and the SGR
formula for 2002 and subsequently; the
stability and the predictability of the
updates; and alternatives to the SGR in the
update. No later than 12 months from
enactment, GAO would be required to
report to Congress on all aspects of
physician compensation for Medicare
services.
The report would review
alternatives to the physician fee schedule.
CRS-39
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Extend Medicare’s private contracting
authority to dentists and podiatrists.
Private contracting allows a physician and
Medicare beneficiary not to submit a claim
for a service which would otherwise be
covered and paid for by Medicare. Under
private contracting, physicians (not
podiatrists or dentists) can bill patients at
their discretion without being subject to
upper payment limits specified by
Medicare. If a physician decides to enter a
private contract with a Medicare
beneficiary, that physician must agree to
forego any reimbursement by Medicare for
all Medicare beneficiaries for 2 years.
Section 603. Doctors of dental surgery or
of dental medicine, doctors of podiatric
medicine, and doctors of optometry will be
able to enter into private contracts with
Medicare beneficiaries. The provision will
be effective upon enactment.
No provision.
Section 604. Doctors of dental surgery or
of dental medicine and doctors of podiatric
medicine would be able to enter into
private contracts with Medicare
beneficiaries.
Require GAO report on geographic
differences in physician payments. No
provision in current law.
Section 413(c). GAO will study payment
differences under the physician fee
schedule for different geographic areas.
The study, including recommendations
concerning use of more current data and
use of cost data rather than price proxies, is
due to Congress within 1 year of the
enactment date.
Section 444. GAO would be required to
study geographic differences in payment
amounts in the physician fee schedule and
report to Congress within 1 year of
enactment.
Section 413. Same provision.
Require GAO report on beneficiary
access to services including concierge
care and impact of these mandatory fees
and/or services on access Periodic
analyses by the Physician Payment Review
Commission, and subsequently MedPAC,
as well as CMS showed that access to
physicians’ services generally remained
good for most beneficiaries through 1999.
More recent surveys convey a more mixed
picture however.
Section 604. GAO is required to conduct
a study on access of Medicare beneficiaries
to physicians’ services under Medicare and
submit a report to Congress on this study
within 18 months of enactment.
Section 650. GAO would study concierge
care provided to Medicare beneficiaries
and its effect on their access to Medicare
covered services and submit a report to
Congress, including recommendations, no
later than 12 months from enactment.
Section 447. GAO would submit a report
to Congress, including recommendations,
regarding the effect of concierge care on
beneficiaries’ access to Medicare covered
services by 12 months from enactment. In
this instance, concierge care would be an
arrangement where a physician or
practitioner charges an individual a
membership fee or other fee or requires the
purchase of an item or service as a
prerequisite for providing the care.
Section 602(a). GAO would be required
to conduct a study on access of Medicare
beneficiaries to physicians’ services under
Medicare including beneficiaries’ use of
services through an analysis of claims data
and the extent to which physicians are not
accepting new Medicare beneficiaries as
patients.
CRS-40
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Require Institute of Medicine (IOM)
study on supply of physicians. No
provision in current law.
No provision.
No provision.
Section 602(b). The Secretary would be
required to request that IOM study the
adequacy of the supply of physicians
(including specialists) in the country and
the factors that affect supply.
The
Secretary would be required to submit the
results of the study in a report to Congress
no later than 2 years from the date of
enactment.
Require MedPAC report on payment
for physician services. No provision in
current law.
Section 303(a). MedPAC is required to
review the payment changes as they affect
payments for items and services furnished
by oncologists and for drug administration
services furnished by other specialists and
submit a report to the Secretary. The
MedPAC report on oncologists’ payments
is due to Congress by January 1, 2006 and
the report on drug administration services
furnished by other specialists is due by
January 1, 2007. The Secretary could
make appropriate adjustments to payments
as part of the rulemaking for physician
payments for 2006.
Section 606. MedPAC is required to
report to Congress on the effects of
refinements to the practice expense
component, by specialty within 1 year of
enactment. A MedPAC report on the
effect of increased physician services on
the well-being of Medicare beneficiaries
and other factors is due within 1 year of
enactment as well.
No provision.
Section 603. MedPAC would be required
to report to Congress on the effects of
refinements to the practice expense
component of payments for physicians’
services after full implementation of the
resource-based payment in 2002.
CRS-41
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Require consultative process before
establishing new evaluation and
management (E&M) codes. Initial E&M
documentation guidelines were issued in
1995 with revisions issued in 1997; both
remain in force today. Approximately 40%
of Medicare payments for physician
services are for services which are
classified as evaluation and management
services (i.e., physician visits). The
Secretary stopped work on the current redraft of E&M codes in order to reassess the
entire effort.
Section 941. The Secretary is prohibited
f r o m i mp le me nting n e w E & M
documentation guidelines unless the
Secretary developed the guidelines in
collaboration with practicing physicians,
established a plan with goals, conducted
pilot projects, and established and
implemented an education program on the
use of the guidelines with appropriate
outreach. Any changes to E&M guidelines
are required to reduce paperwork burden
on physicians.
Section 553.
The Secretary, before
making changes in documentation
guidelines for, providing clinical examples
of, or changing codes for reporting E&M
physician services, would be required to
ensure that the process used in developing
the guidelines, examples, or codes was
widely consultative among physicians,
reflects a broad consensus among
specialties, and would allow verification of
reported and furnished services.
Section 941. The Secretary would be
prohibited from implementing new E&M
documentation guidelines unless the
Secretary developed the guidelines in
collaboration with practicing physicians;
established a plan with goals; conducted
pilot projects;
established and
implemented an education program on the
use of the guidelines with appropriate
outreach. Changes to E&M guidelines
would be required to reduce paperwork
burden on physicians.
Pay for additional hospital outpatient
department (HOPD) mammography
services using physician fee schedule.
Screening mammography coverage
includes the radiological procedure as well
as the physician’s interpretation of the
results of the procedure. The usual Part B
deductible is waived for tests. Payment is
made under the physician fee schedule.
Certain services paid under fee schedules
or other payment systems are excluded
from Medicare’s OPPS-PPS. For
diagnostic mammography services
provided in an HOPD, the technical
component of the fee is paid under the
HOPD PPS.
Section 614. Screening mammography
and diagnostic mammography will be
excluded from OPPS. This provision will
apply to screening mammography services
furnished on or after the date of enactment
a n d will ap p ly to d ia g n o s t i c
mammography services furnished on or
after January 1, 2005.
Section 445. Unilateral and bilateral
diagnostic mammography as well as
screening mammography services would
be paid for under the physician fee
schedule beginning January 1, 2005.
Section 614. Same provision except
effective date would be January 1, 2004.
Pay the physician for
pharmacy
management services. No provision in
current law.
Section 303(e)(2). The Secretary will pay
a dispensing fee (less the applicable
deductible and coinsurance amounts) to
licensed approved pharmacies for covered
immunosuppressive drugs, oral anti-cancer
drugs, and oral anti-nausea drugs used as
part of a chemotherapeutic regimen.
No provision.
Section 303(g). The Secretary would be
required to provide for separate payments
in the physician fee schedule to cover the
administration and acquisition costs
associated with covered drugs and
biologicals furnished by a contractor under
the competitive acquisition program.
CRS-42
Hospital Outpatient Department (HOPD), Ambulatory Surgery Center (ASC), and Clinic Services.
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Hospital Outpatient Department (HOPD) Services
Extend hold-harmless provisions for
small rural hospitals. The outpatient
prospective payment system (OPPS) was
implemented in August 2000 for most
acute care hospitals. Under hold-harmless
provisions, rural hospitals with no more
than 100 beds are paid no less under this
PPS system than they would have received
under the prior reimbursement system for
covered HOPD services provided before
January 1, 2004.
Section 411. The hold-harmless provisions
governing OPPS for small rural hospitals
are extended to HOPD services provided
before January 1, 2006. The Secretary is
required to conduct a study to determine if
the costs, by ambulatory payment
classification (APC) groups, incurred by
rural providers exceed those costs incurred
by urban providers. If appropriate, the
Secretary will provide for a payment
adjustment to reflect the higher costs of
rural providers by January 1, 2006
Section 423. The hold-harmless provisions
governing OPPS reimbursement for small
rural hospitals would be re-established in
2006.
Section 407. The hold-harmless provision
would be extended to January 1, 2006.
The Secretary would be required to
conduct a study to determine if the costs by
ambulatory payment classification (APC)
groups incurred by rural providers exceeds
those costs incurred by urban providers
and provide an appropriate payment
adjustment to reflect the higher costs of
rural providers by January 1, 2005.
Establish hold-harmless provision for
sole community hospitals (SCHs). No
provision in current law.
Section 411. The hold harmless provisions
are extended to SCHs located in a rural
area starting for cost reporting periods
beginning on and after January 1, 2004 and
ending for HOPD services furnished
before January 1,2006.
Section 423.
OPPS hold-harmless
provisions would be extended to SCHs
located in rural areas for services provided
in 2006.
Section 407. The hold-harmless provisions
would be extended to SCHs for 2004 and
2005.
Change hold-harmless provision for
children’s hospitals. OPPS contains a
permanent hold-harmless for cancer
hospitals and children’s hospitals where
payments to these hospitals cannot fall
below what these hospitals would have
received under the payment system in
place before OPPS.
No provision.
Section 450J.
These provisions for
children’s hospitals would be modified so
that those in Maryland (which has a
Medicare waiver) that are paid less under
OPPS than what would have been received
under the prior system or using hospital’s
reasonable operating and capital costs
receive additional payments after October
1, 2003.
No provision.
Increase HOPD payments to small rural
hospitals. Under OPPS, which was
implemented in August, 2000, Medicare
No provision.
Section 424. Medicare’s fee schedule
payments would be increased by 5% for
covered outpatient clinic and emergency
No provision.
CRS-43
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
room visits that are provided by rural
hospitals with up to 100 beds beginning
January 1, 2005 and before January 1,
2008. Beneficiary copayment amounts
would not be affected. The increased
Medicare payments would not be
considered when calculating a rural
hospital’s hold-harmless payment. Budget
neutrality provisions for Medicare’s OPPS
would not apply. Finally, these increased
payments would not affect Medicare
payments for covered outpatient services
after January 1, 2008.
pays for covered services using a fee
schedule based on APCs. Beneficiary
copayments are established as a percentage
of Medicare’s fee schedule payment and
differ by APC. Certain hospitals, including
rural hospitals with no more than 100 beds,
are protected, either on a temporary or on
a permanent basis, from financial losses
that result from implementation of OPPS
under hold-harmless provisions
Increase payments to sole community
hospitals (SCHs) for clinical diagnostic
laboratory tests. Generally, hospitals that
provide clinical diagnostic laboratory tests
under Part B are reimbursed using a fee
schedule. SCHs that provide some clinical
diagnostic tests 24 hours a day qualify for
a 2% increase in the amounts established in
the outpatient laboratory fee schedule; no
beneficiary cost-sharing amounts are
imposed.
No provision.
Section 427. SCHs that provide clinical
diagnostic laboratory tests covered under
Part B in 2005 and 2006 would be
reimbursed their reasonable costs of
furnishing the tests. No beneficiary costsharing amounts would apply to these
services.
No provision.
Establish new payment method for
certain HOPD drugs and biologicals.
Under OPPS, Medicare pays for covered
outpatient drugs in one of three ways: (1)
as a transitional pass-through payment; (2)
as a separate APC payment; or (3) as
packaged APC payment with other
services.
Transitional pass-through
payments are extra payments to cover the
incremental cost associated with certain
Section 621. Starting January 1, 2004,
specified covered HOPD drugs will be
paid based on a percentage of the reference
average wholesale price for the drug. The
percentage of the reference price for solesource drugs manufactured by one entity
can be no less than 88% and no greater
than 95% in CY2004 and no less than 83%
and no greater than 95% in CY2005. The
percentage of the reference price for
Section 436. A new payment method for
certain HOPD drugs and biologicals would
be established for 2005 and 2006. The
drugs and biologicals would be those for
which hospitals received transitional passthrough payments prior to January 1, 2005
that have been assigned to drug-specific
APCs beginning the date of enactment. Or
those that would have been paid in such a
manner but for the application of this
Section 621(a). Starting for services
furnished beginning January 1, 2004,
certain covered HOPD drugs would be
paid no more than 95% of AWP or less
than the transition percentage of the AWP
from CY2004 through CY2006.
In
subsequent years, payment would be equal
to average price for the drug in the area
and year established by the competitive
acquisition program under 1847A. The
CRS-44
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
medical devices, drugs and biologicals that
are inputs to an existing service. The
additional payment for a given item is
established for 2 or 3 years and then the
costs are incorporated into the APC
relative weights.
BBRA specified that
pass-through payments would be made for
current orphan drugs; current cancer
therapy drugs, biologicals, and
brachytherapy; current radiophamaceutical
drugs and biological products; and new
drugs and biological agents. Generally,
CMS has established that a pass-through
payment for an eligible drug is based on
the difference between 95% of its average
wholesale price and the portion of the
otherwise applicable APC payment rate
attributable to the existing drug, subject to
a budget neutrality provision.
innovator multiple source drugs can be no
greater than 68% in CY2004 and CY2005.
The percentage of the reference price for
noninnovator multiple source drugs can be
no greater than 46% in CY2004 and
CY2005. The reference average wholesale
price is the average wholesale price for the
drug as of May 1, 2003. In subsequent
years, payment will equal to the average
acquisition cost for the drug for that year
(which may vary by hospital group taking
into account hospital volume or other
hospital characteristics) or if hospital
acquisition cost data are not available, the
average price for the drug in the year
established under Sections 1842(o), 1847A
or 1847B (which specify Medicare
payments for outpatient drugs covered
under Part B) as calculated and adjusted by
the Secretary. The covered HOPD drugs
affected by this provision are outpatient
drugs that were paid on a pass-through
basis on or before December 31, 2002.
These would not include drugs for which
pass-through payments are first made on or
after January 1, 2003; those drugs for
which a temporary HCPCS code has not
been assigned; or, during 2004 and 2005,
orphan drugs.
Drugs for which a
temporary HCPCS code has not been
assigned will be reimbursed at 95% of the
AWP. Orphan drugs during this 2-year
time period will be paid at an amount
specified by the Secretary.
provision. Payments made under this
provision would be exempt from the
budget neutrality requirement in FY2005
and FY2006. In 2005, these drugs would
be paid as follows: a single source or
orphan product would be paid at 94% of
the AWP existing on May 1, 2003; a
multiple source drug would be paid at 91%
of that existing average wholesale price
(AWP); and a drug with generic versions
would be paid at 71% of that existing
AWP. Those items furnished as part of
other HOPD services would be paid using
the same applicable percentage of the
AWP that would have been determined on
May 1, 2003 if such payment were to have
been made on that date. For 2006, these
payment amounts would be increased by
CPI-U. A private non-profit organization
under contract would determine the
hospital acquisition, pharmacy services,
and handling costs for each of the drugs
paid in this fashion to set payments in 2007
and beyond. This analysis would be
accurate within 3% of the true mean
hospital acquisition and handling costs at a
95% confidence level; begin by January 1,
2005; and be updated annually. Starting
January 1, 2006, a report would be due to
Congress each year.
covered HOPD drugs affected by this
provision are radiopharmaceuticals and
outpatient drugs that were paid on a passthrough basis on or before December 31,
2002. These would not include drugs for
which pass-through payments are first
made beginning January 1, 2003 or those
drugs for which a temporary HCPCS code
has not been assigned. Drugs for which a
temporary HCPCS code has not been
assigned would be reimbursed at 95% of
the AWP. The transition percentage to
AWP for sole-source drugs manufactured
by one entity is 83% in CY2004, 77% in
CY2005, and 71% in CY2006. The
transition percentage to AWP for innovator
multiple source drugs is 81.5% in CY2004,
75% in CY2005, and 68% in CY2006. The
transition percentage to AWP for multiple
source drugs with generic drug competitors
is 46% in CY2004 through CY2006. The
additional expenditures resulting from
these provisions would not be subject to
the budget neutrality requirement. Starting
in CY2004, the Secretary would be
required to lower the threshold for
establishing a separate APC group for
higher costs drugs from $150 to $50 per
administration. These separate drug APC
groups would not be eligible for outlier
payments.
Starting in CY2004,
Medicare’s transitional pass-through
payments for drugs and biologicals
covered under a competitive acquisition
contract would reflect the amount paid
under that contract, not 95% of AWP.
MedPAC will submit a report to the
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Provision and Current Law
H.R. 1 as enacted
Secretary on the payment adjustment to
ambulatory payment classifications for
specified covered outpatient drugs that
takes into account overhead and related
expenses (such as pharmacy services and
handling costs). The Secretary is
authorized to adjust the weights for
ambulatory payment classification based
on such a recommendation. The additional
expenditures that result from the previous
changes will not be taken into account in
establishing the conversion, weighting and
other adjustment factors for 2004 and
2005, but will be taken into account in
subsequent years.
For drugs and biologicals furnished in
2005 and 2006, the Secretary is required
to lower the threshold for establishing a
separate APC group for higher cost drugs
from $150 to $50 per administration.
These separate drug APC groups are not
eligible for outlier payments. Starting in
CY2004, Medicare’s transitional passthrough payments for drugs and
biologicals covered under a competitive
acquisition contract will equal the average
price for the drug or biological for all
competitive acquisition areas calculated
and adjusted by the Secretary for that year.
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
CRS-46
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Limit application of functional
equivalence standards when determining
a drug’s eligibility for transitional pass
though payments. Starting in 2003,
CMS decided that a new anemia treatment
for cancer patients was no longer eligible
for pass-though payments under OPPS,
because it was functionally equivalent
(although not structurally identical or
therapeutically equivalent) to an existing
treatment. The transitional pass-through
rate for the drug was reduced to zero
starting for services in 2003.
Section 622. The Secretary is prohibited
from publishing regulations that apply a
functional equivalence standard to a drug
or biological for transitional pass-through
payments under OPPS. This prohibition
applies to the application of the functional
equivalence standard on or after the date of
enactment, unless such application was
made prior to enactment and the Secretary
applies such standard to the drug only for
the purposes of transitional pass-through
payments. This provision does not affect
the Secretary’s authority to deem a
particular drug to be identical to another
drug if the 2 products are pharmaceutically
equivalent and bioequivalent, as
determined by the Commissioner of the
Food and Drug Administration.
Section 437. The Secretary would not be
able to apply this standard to a drug or
biological for transitional pass-through
payments under OPPS. This prohibition
would apply, unless such a standard was
made prior to enactment and only for the
purposes of transitional pass-through
payments. The Secretary would still be
able to deem a particular drug as identical
to another drug if the two products are
pharmaceutically equivalent and
bioequivalent, as determined by FDA.
Section 621(c). The Secretary would be
prohibited from applying a “functional
equivalence” standard or any similar
standard in order to deem a particular drug
or biological to be similar or functionally
equivalent to another drug unless the
Commissioner of FDA establishes such a
standard and certifies that the two products
are functionally equivalent. The Secretary
would be able to implement this standard
after meeting applicable rulemaking
requirements. The provision prohibits the
application of this standard to a drug or
biological prior to June 13, 2003.
Establish separate payments for certain
brachytherapy devices. In Medicare’s
OPPS, current drugs and biologicals that
were eligible for transitional pass-through
payments on or prior to January 1, 2000,
were removed from that payment status
effective January 1, 2003.
CMS
established separate APC payments for
certain of these drugs. Other drugs such as
brachytherapy seeds (radioactive isotopes
used in cancer treatments) were packaged
into payments for brachytherapy
procedures.
Section 421(b). From January 1, 2004
through December 31, 2006, Medicare’s
payments for brachytherapy devices will
equal the hospital’s charges adjusted to
cost. Charges for such devices will not be
included in determining any outlier
payments. The Secretary is required to
create separate APCs to pay for these
devices that reflect the number, isotope,
and radioactive intensity of such devices,
including separate groups for palladium103 and iodine-125 devices. GAO is
required to study the appropriateness of
payments for brachytherapy devices and
submit a report including
recommendations to Congress and to the
Secretary no later than January 1, 2005.
Section 450A. The Secretary would be
required to conduct a budget neutral, 3year demonstration project that would
exclude brachytherapy devices from the
OPPS and make payment on the basis of
the hospital’s charges for each device,
adjusted to cost. The Secretary would be
required to create separate, additional
groups of covered HOPD services for
brachytherapy devices to reflect the
number, isotope, and radioactive intensity
of such devices.
Section 621(b). From 2004 through
2006, payments for brachytherapy devices
would equal the hospital’s charges adjusted
to cost. The Secretary would be required
to create separate APCs to pay for these
devices that reflect the number, isotope,
and radioactive intensity of such devices.
This would include separate groups for
palladium-103 and iodine-125 devices.
GAO would submit a report to Congress
on the appropriateness of such payments
no later than January 1, 2005.
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Provision and Current Law
H.R. 1 as enacted
Require hospital acquisition study. No
provision in current law
Section 621(a). GAO will conduct an
acquisition cost survey for each specified
covered drug in 2004 and 2005. No later
than April 1, 2005, GAO will furnish this
survey data to set 2006 payment rates.
GAO will submit a report to Congress on
2006 rates no later than 30 days after
issuance of the proposed rule setting forth
these rates.
GAO will submit
recommendations regarding the survey
methodology and
frequency to the
Secretary who will conduct periodic
surveys to set subsequent payment rates.
S. 1 (as passed the Senate)
No provision.
H.R. 1 (as passed the House)
Section 621(d). The Secretary would
study the hospital acquisition costs related
to covered outpatient drugs that cost $50
per administration and more that are
reimbursed under the OPPS.
Ambulatory Surgery Center Services (ASCs)
Reduce ambulatory surgery center
(ASC) update. Medicare uses a fee
schedule to pay for the facility services
related to a surgery provided in an ASC.
From FY1998 through FY2002, the update
was established as the CPI-U minus 2.0
percentage points, but not less than zero.
In 2003 and subsequent years, the update is
CPI-U.
Section 626. In FY2004, starting April 1,
2004, the ASC update will be the CPI-U
(estimated as of March 31, 2003) minus
3.0 percentage points. In FY2005, the last
quarter of calendar year 2005, and each of
the calendar years 2006 through 2009 the
update will be 0%. A revised payment
system for surgical services furnished in an
ASC will be implemented on or after
January 1, 2006 and not later than January
1, 2008. It will be budget neutral in its
implementation year. There will be no
administrative or judicial review of the
ASC classification system, relative
weights, payment amounts and any
geographic adjustments. GAO will study
the relative costs of ASC procedures.
No provision.
Section 625. The reduction in the update
would be reestablished for FY 2004 - FY
2008. ASCs would get an increase
calculated as the CPI-U minus 2.0
percentage points (but not less than zero)
in each of the fiscal years from 2004
through 2008.
CRS-48
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Rural Health Clinics (RHCs) and Federally Qualified Health Clinics (FQHCs) Services
Increase payments for rural health
clinics. BBA 1997 extended the per visit
payment limits that had existed for
independent rural health clinics to
provider-based rural health clinics (RHC)
except for those clinics based in small rural
hospitals with fewer than 50 beds. For
services rendered from January 1, 2003
through February 28, 2003, the RHC upper
payment limit is $66.46, which reflects a
2.6% increase in 2002 payment limit as
established by the 2002 Medicare
Economic Index (MEI). For services
rendered from March 1, 2003 through
December 31, 2003, the Medicare RHC
upper payment limit is $66.72, which
reflects a 3.0% increase in the 2002
payment limit as established by the 2003
MEI. The 2002 MEI was used as an
update for 3 months because of the delayed
implementation.
No provision.
Section 428. The RHC upper payment
would be increased to $80.00 for calendar
year 2005. The MEI applicable to primary
care services would be used to increase the
payment limit in subsequent years.
No provision.
Covered Part B Outpatient Drugs (Not Provided by a HOPD).
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Pay for existing outpatient drugs
provided incident to a physician’s
services. Although Medicare does not
currently have an outpatient prescription
drug benefit, it covers approximately 450
outpatient drugs and biologicals authorized
by statute, including those: (1) that are
Section 303(b) In general, payments for
most covered Part B drugs, including
intravenous immune globulin, furnished in
2004 will equal 85% of the average
wholesale price (determined as of April 1,
2003). Certain categories of drugs and
biologicals (drug products) will continue to
Section 432(a). In 2004, existing drugs
(available by April 1, 2003) would be paid
the lower of the widely available market
price or 85% of the listed AWP as of Apr.
1, 2003 as subsequently increased by the
CPI for medical care as of June. The
Secretary would be required to determine
Section 303(b). Physicians who opt out of
the competitive acquisition program
(which is described subsequently) would
be paid under a new, separate 1847B
payment method. Subject to the
beneficiary cost-sharing, non-generic drugs
would be paid 112% of the applicable
CRS-49
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
covered if they are usually not selfadministered and are provided incident to
a physician’s services; (2) those that are
necessary for the effective use of covered
durable medical equipment; (3) certain
self-administered oral cancer and antinausea drugs (those with injectable
equivalents; (4) erythropoietin (used to
treat anemia); (5) immunosuppressive
drugs after covered Medicare organ
transplants; (6) hemophilia clotting factors;
and (7) vaccines for influenza, pneumonia,
and hepatitis B. Payments are based on
95% of the average wholesale price (AWP)
published in industry reference
publications. AWP does not account for
discounts routinely offered to providers
and physicians.
Current Medicare
payment rates are 95% of AWP for brand
name drugs produced by a single
manufacturer (or single source drugs).
Medicare will pay 95% of the lower of (a)
the median AWP of all generic drugs or (b)
the lowest brand-name product AWP for
drugs with two or more competing brand
names (or multiple source drugs) or those
drugs with available generic equivalents.
Although Medicare uses the Healthcare
Common Procedure Coding System
(HCPCS) codes to pay for physician
administered drugs, the AWPs are
established for national drug codes (NDC)
which provides data on chemical molecule,
drug manufacturer, dosage, dosage form
and package size.
be paid at 95% of the AWP including
blood products and clotting factors
furnished during 2004; a drug product
furnished during 2004 that was not
available for Part B payment as of April 1,
2003; pneumococcal, influenza, and
hepatitis B vaccines; and a drug or
biological (other than erythropoietin)
furnished in connection with renal dialysis
services that are separately billed by renal
dialysis facilities. Drug products paid at
85% of AWP in 2004 may be paid a
different amount if the widely available
market price is different than the payment
amount for the year. Also payments may
be adjusted because of data submitted by
the manufacturer or by another entity by
October 15, 2003. In no case will payment
be less than 80% of AWP.
whether the widely available market price
is different from the AWP amounts using
any HHS-IG or GAO report issued in 2000
and later as well as other data from
purchaser, supplier and manufacturers. If
different, the widely available market price
would be treated as the AWP amount in
2004 and subsequently. However, if that
difference is more than 15%, payments
would be reduced in 15% increments of
Medicare’s prior year payment. This
transition would not apply to those with
generic versions in the market beginning
2004. After Jan. 1, 2004, payments for
covered vaccines would be equal to the
AWP.
price in 2005 and 2006 and 100% of the
price subsequently. The multiple source
drug applicable price would be the
reported volume-weighted average of the
average sales price; the applicable price for
a single source drug would be the lesser of
the manufacturer’s average sales price
(ASP) for the NDC code or the reported
wholesale acquisition cost (WAC).
Payments would not account for special
packaging, labeling or identifiers on the
dosage form or product or package. By
April 1, 2004, the ASP would be
calculated by NDC each calendar quarter
by dividing a manufacturer’s total sales by
the units sold in that quarter with certain
adjustments to account for volume
discounts and other rebates. Certain sales
would be exempt from the calculation.
The WAC would be the manufacturer’s list
price to wholesalers or direct purchasers
for the most recent available month, not
including discounts or other price
reductions, as reported in wholesale price
guides or other pricing publications.
Payment rates would be updated on a
quarterly basis. Certain contractors would
determine the payment amounts. Certain
standards would define multiple and single
source drugs and establish pharmaceutical
equivalence. There would be no
administrative or judicial review of the
ASP.
Section 303(c) Beginning in 2005, drug
products, except for pneumococcal,
influenza, and hepatitis B vaccines, those
associated with certain renal dialysis
services, blood products and clotting
factors and radiopharmaceuticals, will be
paid using either the average sales price
methodology or through the competitive
acquisition program. Medicare’s payment
under the average sales price (ASP)
methodology will equal 106% of the
applicable price for a multiple source drug
or single source drug subject to beneficiary
deductible and coinsurance amounts. The
applicable price for multiple source drugs
is the volume-weighted average of the
average sale price calculated by NDC code
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Provision and Current Law
H.R. 1 as enacted
for each calendar quarter. The applicable
price for single source drugs is the lesser of
the average sales price or the wholesale
acquisition cost. Certain sales such as
those to the Medicaid drug rebate program
are exempt from the calculation, but the
ASP will take into account certain
discounts (not including Medicaid rebates).
After 2004, the Secretary may include
other price concessions recommended by
the HHS-IG who will conduct market
surveys. If the ASP exceeds the market
price or average manufacturer price by a
threshold percentage, the ASP may be
disregarded. In 2005 the threshold is 5%;
in 2006 and subsequent years, the
percentage threshold will be specified by
the Secretary. The payment amount will
then be equal to the lesser of the widely
available market price or 103% of the
average manufacturer price. For drugs
furnished in a year after 2004, the widely
available market price is the price that a
prudent physician or supplier would pay
for a drug product, taking into account
certain routinely available discounts. The
wholesale acquisition cost or other
reasonable measure may be used instead of
the manufacturer’s average sale price in
the case of certain public emergencies.
There will be no administrative or judicial
review of determinations of payment
amounts; the identification of units and
package size; or the method used to
allocate price concessions to a specific
quarter among other items.
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
CRS-51
Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
H.R. 1 (as passed the House)
Pay for new outpatient drugs provided
incident to a physician’s services. See
above.
Section 303(c). Drug products during an
initial period (not to exceed a full calendar
quarter) when data on the prices for sales is
not sufficiently available to compute ASP
will be paid based on the wholesale
acquisition cost or on the payment methods
in effect as of November 1, 2003.
Section 432(a) continued. New drugs
(available after April 1, 2003) would be
paid based on the manufacturer’s estimated
price data. During the first and second
years, the manufacturer would provide data
on the actual market prices paid by
physicians or suppliers which would be
equal to the lesser of the AWP or the
original estimate. Subsequently, payments
would be equal to the lesser of the AWP or
the widely available market price
established for existing drugs. If no
market price exists, the prior year’s
payment is increased by June’s CPI for
medical care. Other payment changes for
the administration of drugs would be
contingent on the implementation of these
provisions.
Section 303(b) continued. New drugs.
The Secretary would be able to disregard
the average sales price during the first
quarter of a new drug’s sales if the price
data is not sufficient to determine an
average amount payable.
Establish competitive pricing program
as an establish alternative pricing
method for physicians who elect not to
participate in competitive bidding
program. See above
Section 303(d). Under the new Section
1847B, the Secretary is required to
establish a competitive acquisition
program to acquire and pay for
competitively biddable drug products. The
Secretary is required to compute an area
average of the bid prices submitted, in
contract offers accepted for the category
and the area, for each year or other
contract period. Medicare’s program
payment for these drugs will equal 80% of
the average bid price after the Medicare
beneficiary meets the applicable
deductible. Generally, coinsurance and
deductible amounts will be collected by the
contractor that supplies the drug product.
There shall be no administrative or judicial
review with respect to the establishment of
See above.
Section 303(b).
Under new section
1847A, the Secretary would establish a
competitive acquisition program to acquire
and pay for covered outpatient drugs.
Under this program, at least two
contractors would be established in each
competitive acquisition area (which would
be defined as an appropriate geographic
region) throughout the United States. Each
year, a physician would be able to select a
contractor who would deliver covered
drugs and biologicals to the physician; as
discussed above, a physician would be able
to elect payment under the ASP payment
methodology established by 1847B. Blood
clotting factors, drugs and biologicals
furnished as treatment for end-stage renal
disease (ESRD), radiopharmaceuticals, and
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Provision and Current Law
H.R. 1 as enacted
S. 1 (as passed the Senate)
vaccines would not be considered covered
drugs under the competitive acquisition
program.
payment amounts, contract awards,
establishment of competitive acquisition
areas, the phased-in implementation, the
selection of categories of competitively
biddable drugs and biologicals for
competitive acquisition, or the bidding
structure or number of contractors who are
selected. No later than July 1, 2008, the
Secretary is required to report to Congress
on savings, reductions in cost-sharing,
access to competitively biddable drugs and
biologicals, the range of choices of
contractors available to providers as well
as beneficiary and provider satisfaction
under the competitive acquisition program.
Establish contracting requirements for
competitive acquisition program. No
provision in current law.
Section 303(d)
Certain contractor
selection and contracting requirements for
the competitive acquisition program are
established. Specifically, the Secretary is
required to establish an annual selection
process for a contractor in each area for
each category of drugs and biologicals.
The Secretary may not award the 3-year
contract to any entity that does not have
the capacity to supply the drug products or
does not meet established quality, service,
fi
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