Medicare Program; Use of Repayment Plans, 36443-36448 [E8-13520]
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Federal Register / Vol. 73, No. 125 / Friday, June 27, 2008 / Rules and Regulations
PART 52—[AMENDED]
I. Background
1. The authority citation for part 52
continues to read as follows:
A. Medicare Overpayment
Medicare overpayments are Medicare
funds an individual, provider, or
supplier has received that exceed
amounts due and payable under the
Medicare statute and regulations (plus
any applicable interest and penalties
assessed on the overpayment). Section
400.202 defines a ‘‘supplier’’ as ‘‘a
physician or other practitioner, or an
entity other than a provider, that
furnishes health care services under
Medicare.’’
Generally, overpayments result when
payment is made by Medicare for items
or services that are not covered, exceeds
the amount allowed by Medicare for an
item or service, or is made for items or
services that should have been paid by
another insurer (for example, Medicare
secondary payer obligations). Once a
determination and any necessary
adjustments in the amount of the
overpayment have been made, the
remaining amount is a debt owed to the
United States Government.
Section 1870 of the Social Security
Act (the Act) provides a framework
within which liability for such Medicare
overpayments is determined and
recoupment of overpayments is
pursued. This framework prescribes a
decision making process that the agency
follows when pursuing the recoupment
of Medicare overpayments.
The regulation governing the liability
for Medicare overpayments is located at
42 CFR part 401 (subpart F).
I
Authority: 42 U.S.C. 7401 et seq.
Subpart WW—Washington
2. Section 52.2475 is amended by
adding paragraph (a)(4) to read as
follows:
I
§ 52.2475
Approval of plans.
(a) * * *
(4) Vancouver.
(i) EPA approves as a revision to the
Washington State Implementation Plan,
the Vancouver Air Quality Maintenance
Area Second 10-year Carbon Monoxide
Maintenance Plan submitted by the
Washington Department of Ecology on
April 25, 2007.
(ii) [Reserved]
*
*
*
*
*
[FR Doc. E8–14518 Filed 6–26–08; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 401
[CMS–6032–F]
RIN 0938–AO27
Medicare Program; Use of Repayment
Plans
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Final rule.
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AGENCY:
SUMMARY: This final rule modifies
Medicare regulations to implement
section 935(a) of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 pertaining to
the use of repayment plans (also known
as extended repayment schedules or
‘‘ERS’’) for Medicare provider and
supplier overpayments. Under this
provision, we are granting a provider or
a supplier an ERS under certain terms
and conditions as defined in the statute.
This final rule establishes criteria and
procedures to apply this requirement
and to define the concepts of
‘‘hardship’’ and ‘‘extreme hardship.’’
DATES: Effective Date: These regulations
are effective on July 28, 2008.
FOR FURTHER INFORMATION CONTACT: Tom
Noplock, (410) 786–3378.
SUPPLEMENTARY INFORMATION:
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B. Statutory Authority
The Federal Claims Collection Act of
1966 (Pub. L. 89–508) (FCCA), 80 Stat.
308 (amended by the Debt Collection
Improvement Act of 1996 (Pub. L. 104–
134) (DCIA) (codified at 31 U.S.C. 3711))
is the Federal government’s basic
statutory authority for debt management
practices. The Congress intended the
FCCA to reduce the amount of litigation
previously required to collect claims
and to reduce the volume of private
relief legislation in the Congress. The
FCCA was intended to be independent
of the other authorities we use to collect
debt and added to, rather than
supplanted, our other authorities,
including common law authority.
The FCCA authorized the head of an
agency to collect claims in any amount.
This statute also provided that the head
of an agency may, under certain
conditions, compromise a claim, or
suspend or terminate collection action
on a claim. Uncollectible claims in
excess of $100,000, exclusive of interest,
must be referred to the Department of
Justice for compromise. The FCCA was
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amended in 1996 and is now referred to
as the Debt Collection Improvement Act
of 1996 (Pub. L. 104–134) (DCIA), 110
Stat. 1321, 1358 (April 26, 1996)
(codified at 31 U.S.C. 3711).
In the November 2, 1977 Federal
Register (42 FR 57351), the Secretary of
the Department of Health and Human
Services (the Secretary) published a rule
to delegate authority to the Department
Claims Officer generally, and the
Administrator of the Centers for
Medicare & Medicaid Services (the
Administrator) for necessary claims
collection actions under our programs.
The authority delegated to the
Administrator covers all of our activities
in the Medicare program (Title XVIII)
and pertains to claims up to $20,000.
(This amount has been increased to
$100,000; see 31 U.S.C. 3711.)
In the August 29, 1983 Federal
Register (48 FR 39060), we published
the ‘‘Federal Claims Collection Act;
Claims Collection and Compromise’’
final rule with comment period in
accordance with the FCCA. In that final
rule with comment period, we adopted
the applicable debt collection tools
made available to us under the FCCA
including the ability to collect or
compromise claims, or suspend or
terminate collection action, as
appropriate. The final rule with
comment period also set forth the
requirements we use to evaluate
debtors’ requests for extended
repayment agreements specified in
§ 401.607.
As part of the Health Insurance
Portability and Accountability Act of
1996 (Pub. L. 104–191) (HIPAA), the
Congress added section 1893 to the Act
establishing the Medicare integrity
program (MIP) to carry out Medicare
program integrity activities that are
funded from the Medicare Trust Funds.
Section 1893 of the Act expands our
contracting authority to allow us to
contract with eligible entities to perform
MIP activities. These activities include
review of provider and supplier
activities including medical, fraud, and
utilization review; cost report audits;
Medicare secondary payer
determinations; education of providers,
suppliers, beneficiaries, and other
persons regarding payment integrity and
benefit quality assurance issues; and
developing and updating a list of
durable medical equipment items that
are subject to prior authorization (42
U.S.C. 1395ddd). These MIP contractors
assist us in the identification and
collection of Medicare provider and
supplier overpayments.
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C. Overview of Current Policy
The current policy that CMS and its
contractors use for the evaluation of
extended repayment schedules (ERSs) is
based on the existing regulations at
§ 401.607(c)(2) and guidance in the
Medicare Financial Management
Manual, Pub. 100–6 (Chapter 4, Section
50). Under our current policy, we
determine the frequency and amount of
the installment payments based on the
factors set forth at the current
§ 401.607(c)(2) which include the
following: (1) The amount of the claim;
(2) the debtor’s ability to pay; and (3)
the cost to CMS of administering an
installment agreement.
Under the current ERS review
process, we primarily focus on the
second factor, the debtor’s ability to
repay the overpayment, by conducting a
review of the debtor’s financial status,
similar to how banks assess applicants
for a loan. In almost all cases, we try to
work with the provider or supplier to
recover the overpayment. In general, it
has been our experience that it is in
both CMS and the debtor’s best interests
to work out a reasonable repayment
schedule to recoup an overpayment
rather than demand immediate
collection of the debt within 30 days,
which could place a provider or
supplier at financial risk or bring the
provider or supplier a step closer to
bankruptcy.
Under our existing procedures we
review financial documentation
submitted by the provider or supplier to
assess the provider’s or supplier’s
ability to repay the Medicare
overpayment. This documentation must
include, at a minimum, a statement of
financial position (for example, a
balance sheet), a statement of financial
performance (for example, an income
statement), and a statement of future
viability (for example, a projected
statement of cash flow). In addition, the
provider must include a letter from a
financial institution proving that it
cannot obtain financing from an
alternative source.
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D. Medicare Prescription Drug,
Improvement, and Modernization Act of
2003
On December 8, 2003, the Congress
enacted the Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (Pub. L. 108–173) (MMA). This
legislation contained provisions
affecting the recovery of provider and
supplier overpayments under the
Medicare program. Section 935(a) of the
MMA amended title XVIII of the Act by
adding a new section 1893(f)(1) to the
Act to require us to use certain statutory
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criteria in evaluating whether a provider
or supplier should be granted a
repayment schedule of at least 6 months
and up to 5 years.
II. Provisions of the Proposed
Regulations
The following is an overview of the
provisions we proposed in the Use of
Repayment Plans proposed rule
published in the November 27, 2006
Federal Register (71 FR 68519).
1. Hardship Provision
Under section 1893(f)(1) of the Act,
we may grant a provider or a supplier
upon request, a repayment schedule of
at least 6 months, if repaying an
overpayment within 30 days would
constitute a ‘‘hardship’’ on the provider
or supplier, provided that certain
criteria are met.
The new statute at section
1893(f)(1)(B)(i) of the Act defines
‘‘hardship’’ based on the relationship
between the amount of the Medicare
overpayment(s) not covered under an
existing ERS owed by a provider or
supplier and the total amount of
Medicare payments made to that
provider or supplier over the most
recently submitted cost report or for the
previous calendar year.
Under section 1893(f)(1)(B) of the Act,
a provider or supplier’s repayment of an
overpayment within 30 days is deemed
to be a ‘‘hardship’’ when the total
amount of all outstanding overpayments
not included in an approved existing
repayment schedule is 10 percent or
greater than the total Medicare
payments made for the cost reporting
period covered by the most recently
submitted cost report (for a provider
filing a cost report), or the previous
calendar year (for a supplier or non cost
report provider). We proposed to
interpret ‘‘outstanding overpayments’’
to include both principal and accrued
interest. We read the newly added
section 1893(f)(1)(B)(iii) of the Act to
exclude overpayments already being
repaid under an approved ERS.
We proposed to interpret the new
‘‘hardship’’ test under section 935(a) of
the MMA as not to supersede our ERS
regulations currently at § 401.607(c)(2),
(which we proposed to redesignate as
§ 401.607(c)(3)). Since our existing
regulations governing ERSs are issued
under the FCCA, we do not plan to
eliminate the criteria and procedures
currently used to grant providers and
suppliers ERSs. Instead, we proposed to
add an initial ‘‘hardship’’ test to existing
regulations and procedures for
determining a debtor’s ERS.
We proposed that all requests for an
ERS first be evaluated under the new
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‘‘hardship’’ test. Under section 935(a) of
the MMA, if ‘‘hardship’’ is determined
and no statutory exception applies
under § 401.607(c)(2)(iv), then the
statute requires that the Secretary grant
a provider or supplier a repayment
period of at least 6 months but not
longer than 3 years.
Section 935(a) of the MMA requires
that the Secretary establish rules for
cases when a provider or a supplier was
not paid during the previous year or
paid for only a portion of that year. For
these cases, we proposed to use the last
12 months of Medicare payments made
to the provider or supplier. In cases
where there is less than a 12-month
payment history, we proposed that the
number of months available be
annualized to equal an approximate
yearly Medicare payment level for the
provider or supplier. (For detailed
examples on how to apply the new
‘‘hardship’’ test provided in section
1893(f)(1) of the Act, please see the
November 27, 2006 proposed rule, ‘‘Use
of Repayment Plans’’ (71 FR 68521).)
2. Exceptions Under the ‘‘Hardship’’
Provision in Section 935(a) of the MMA
Section 935(a) of the MMA sets out
exceptions to granting a provider or
supplier an extended repayment
schedule even if the provider or
supplier meets the ‘‘hardship’’ test.
These exceptions occur when there is
reason to suspect the provider or
supplier may file for bankruptcy, cease
to do business, discontinue
participation in the program, or when
there is an indication of fraud or abuse
committed against the program. (We
proposed that contractors continue to
use existing procedures and definitions
applicable to bankruptcy and fraud or
abuse.) In such cases, CMS or its
contractors are prohibited from granting
an ERS.
3. Extreme Hardship Provision
Under the provisions of
§ 401.607(c)(2)(vi) of this final rule, the
Secretary may grant a provider or a
supplier a repayment schedule of 36
months and up to 60 months if repaying
an overpayment would constitute an
‘‘extreme hardship’’ unless a statutory
exception applies under
§ 401.607(c)(2)(iv). Since the Congress
left the definition of ‘‘extreme hardship’’
to our discretion, we considered
different approaches for defining
‘‘extreme hardship’’ and sought public
comment on this section.
We considered proposing a new
financial threshold to determine if a
provider or supplier was in extreme
financial hardship, such as using a 15
percent threshold. We rejected this
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approach because it could result in
discriminating against providers and
suppliers who may be similarly
financially situated but may attribute
more of their total revenue to Medicare
income. This could occur for example
with a home health agency (HHA)
which may attribute 100 percent of its
revenue to Medicare business and a
skilled nursing facility (SNF) which
may only attribute 20 percent of its
business to Medicare.
We proposed to define ‘‘extreme
hardship’’ when a provider or supplier
qualifies under the ‘‘hardship’’
provision defined above and the
provider’s or supplier’s request for an
ERS is approved under newly
redesignated § 401.607(c)(3). If we
determine the request meets the criteria
in the redesignated § 401.607(c)(3) and
meets the CMS manual guidance set
forth in the Medicare Financial
Management Manual, Pub. 100–6,
Chapter 4, Section 50, we proposed that
the provider or supplier may be granted
an ERS between 36 and 60 months. We
also proposed that contractors apply the
statutory exceptions to ‘‘extreme
hardship’’ cases in a similar manner as
they do to ‘‘hardship’’ cases. We
solicited comments on other alternative
approaches to define ‘‘extreme
hardship’’ that could distinguish
between the most extreme cases
requiring ERSs between 36 and 60
months.
4. Extended Repayment Schedules
(ERSs)
We proposed to initially handle ERS
requests differently than we have under
our current regulations. We proposed to
allow providers or suppliers that meet
the ‘‘hardship’’ test and request only a
6-month ERS period, the opportunity to
pay back the Medicare debt in 6 months
without having to submit financial
documentation to the contractor in
accordance with the existing
instructions in the Medicare Financial
Management Manual, CMS, Pub. 100–6,
Chapter 4, Section 50. We believe that
by waiving the requirement to submit
financial documentation (such as
financial statements or a bank denial
letter) for a 6-month ERS, we allow a
provider or supplier time to generate or
secure the necessary capital to liquidate
the debt without having to file extensive
documentation in order to secure a
repayment schedule.
We therefore proposed that a provider
or supplier that requests a 6-month ERS,
meets the ‘‘hardship’’ test, does not fall
within an exception, and elects not to
submit financial documentation would
be approved for a 6-month ERS. Any
provider or supplier qualifying for the 6-
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month ERS under the ‘‘hardship’’
provision has the choice to turn down
the 6-month ERS and either pay off the
debt within 30 days of the date of
determination or request a longer than
6-month ERS. In addition, we proposed
not to prohibit any provider or supplier
under the 6-month ‘‘hardship’’
provision ERS from applying for a
longer ERS if it later desires to do so
under § 401.607(c)(3).
For all ERS requests greater than 6
months, we proposed to rely on current
regulations and procedures that require
the provider or supplier to submit
financial documentation in accordance
with the Medicare Financial
Management Manual, CMS Pub. 100–6,
Chapter 4, Section 50. A provider or
supplier must continue to submit a
written request that refers to the specific
overpayment for which an ERS is being
requested, the number of months
requested in the ERS, and include the
first payment with its request. The
contractor would determine the
duration of the ERS based on its review
of the provider or supplier’s
documentation in accordance with CMS
manual guidance.
If a provider or supplier misses one
installment payment in any ERS granted
under section 935(a) of the MMA, the
statute permits us to immediately
collect the entire overpayment.
However, we proposed to impose this
penalty only on the ‘‘automatic’’ 6month ERS. With all other ERSs, we
proposed to continue to use the existing
procedures that define a default of an
ERS as missing two consecutive
installment payments.
We proposed to revise § 401.601(a) to
read as follows: ‘‘This subpart
implements the following provisions:
(1) For CMS the Debt Collection
Improvement Act of 1996 (Pub. L. 104–
134) (DCIA), 110 Stat. 1321, 1358 (April
26, 1996) (codified at 31 U.S.C. 3711),
and conforms to the regulations (31 CFR
parts 900–904) issued jointly by the
Department of the Treasury and the
Department of Justice that generally
prescribe claims collection standards
and procedures under the DCIA for the
Federal government; (2) section
1893(f)(1) of the Act regarding the use
of repayment plans.’’
In addition, in § 401.603 we proposed
to add a definition for an ‘‘extended
repayment schedule.’’
We proposed to redesignate
§ 401.607(c)(2) as § 401.607(c)(3). In
addition, we proposed a new
§ 401.607(c)(2), Extended repayment
schedule, in accordance with section
1893(f)(1) of the Act. We proposed to
implement the provisions of section
1893(f)(1) of the Act, as amended by
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36445
section 935(a) of the MMA, in new
§ 401.607(c)(2), Extended repayment
schedule.
III. Analysis of and Responses to Public
Comments
We received 6 public comments on
the November 27, 2006 proposed rule.
The following is a summary of the major
issues and our responses.
Comment: One commenter believed
that the provisions of the proposed rule
were not equitable between provider
types because 10 percent of total
Medicare reimbursement for a provider
with a 50 percent Medicare fee-forservice revenue is a greater threshold to
reach than a provider with a 5 percent
Medicare fee-for-service revenue.
Response: We agree with the
comment that the proposed rule may
not in all cases treat different provider
types similarly. However, the statute
was written to define hardship as a ratio
of Medicare overpayments to total
Medicare payments/reimbursement in a
given time period. The statute does not
allow CMS to take into account the
percentage of patient revenue from other
sources when defining ‘‘hardship.’’ For
all other ERS requests, we proposed to
rely on current regulations and
procedures that require the provider or
supplier to submit financial
documentation in accordance with the
Medicare Financial Management
Manual, CMS Pub. 100–6, Chapter 4,
Section 50.
Comment: Some commenters believed
it would be more consistent and more
fair to providers if we would use the
definition of default for all ERSs as
missing two consecutive installment
payments.
Response: While the statute permits
us to immediately collect on an entire
overpayment if a provider or supplier
misses one installment payment in any
ERS granted under section 935(a) of the
MMA, we have decided to impose the
1-month missed payment rule only for
the 6-month ‘‘hardship-based’’ ERS. We
chose not to apply the two missed
payment rule to 6-month ERSs because
we do not want a provider or supplier
to be too far in arrears if they miss
payments in such a short ERS. A
provider or supplier that is behind two
payments in a 6-month ERS has a
greater amount of its payments in
arrears than a provider or supplier that
is behind two payments in a 36-month
or 60-month ERS. For example, two
missed payments on the amortization of
an overpayment covered under a 6month ERS (2 divided by 6) is equal to
approximately 33.3 percent of the total
overpayment whereas 2 missed
payments under a 36-month ERS (2
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divided by 36) is equal to a much lower
5.5 percent of the total overpayment. On
a 60-month ERS, two missed payments
would only equal 3.3 percent of the total
overpayment (2 divided by 60).
Comment: Some commenters were
concerned that we may be inadvertently
legally binding providers to the
‘‘automatic’’ 6-month ERS and not
offering providers a future opportunity
to request a second ERS under
§ 401.607(c).
Response: In the proposed rule, we
stated that any provider or supplier
qualifying for the 6-month ERS under
the ‘‘hardship’’ provision has the choice
to turn down the 6-month ERS and
either pay off the debt within 30 days
of the date of determination or request
a longer ERS under newly redesignated
§ 401.607(c)(3). In addition, we will not
prohibit any provider or supplier under
the 6-month ‘‘hardship’’ provision ERS
from applying for a longer ERS if it later
desires to do so under § 401.607(c)(3).
Comment: One commenter believed
that there is no practical reason for why
we have not adopted a parallel
numerical threshold approach to
extreme hardship by using some
percentage above the numerical 10
percent threshold for hardship.
Response: The 10 percent used in this
final rule to define hardship is required
by statute. As stated in the proposed
rule, we considered proposing a new
financial threshold to determine if a
provider or supplier was in extreme
financial hardship, such as using a 15
percent threshold. However, we rejected
this approach because it could result in
discriminating against providers and
suppliers who may be similarly
financially situated but may attribute
more of their total revenue to Medicare
income. This could occur for example
with a home health agency (HHA)
which may attribute 100 percent of its
revenue to Medicare business and a
skilled nursing facility (SNF) which
may only attribute 20 percent of its
business to Medicare. In addition, the
ERS review process is a multivariable
financial analysis and it would not be
practical or equitable to either the
provider/supplier or the Medicare
program to reduce the ERS process
down to a single variable. We believe
keeping the definition of extreme
hardship broader than a single variable
is in the best interests of the provider
and supplier community and is the most
effective way to ensure that
overpayments will be collected and
returned to the Medicare Trust Fund.
Comment: One commenter stated that
there is confusion as to why the burden
of producing financial documentation
can be removed for the ‘‘automatic’’ 6-
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month ERS but not for ERS plans longer
than 6 months.
Response: We removed the financial
documentation requirement for 6-month
ERSs because the contractor already has
the requisite information needed to
determine if a provider or supplier
meets the statutory hardship test.
However, in order to grant an ERS
longer than 6 months, we continue to
need financial documentation to
determine a provider or supplier’s
ability to make future ERS payments.
We also need financial data to
determine the length of the ERS or
payback period that should be granted
to the provider or supplier. While a
short ERS may cause a provider or
supplier to go out of business, the longer
the ERS period the greater the delay in
the overpayment recovery and the
greater the financial risk to the Medicare
program. We believe the increased risk
associated with a longer repayment or
amortization period requires that we
give an ERS request greater financial
scrutiny.
Comment: We received comments
that were outside the scope of the
proposed rule (for example, regarding
the effects on State Medicaid programs).
Response: We are not responding in
this final rule to comments that are
outside of the scope of the proposed
rule.
IV. Provisions of the Final Regulations
As a result of our review of the public
comments, we do not find any cause to
alter the provisions of the proposed
rule. Therefore, we are finalizing the
provisions as proposed.
V. Collection of Information
Requirements
This final rule does not impose any
new information collection or
recordkeeping requirements. The
information collection requirements
discussed in the preamble pertain to the
extension of repayment schedules. The
requirements and associated paperwork
burden are approved under Office of
Management and Budget (OMB) control
number 0938–0270, with a current
expiration date of January 31, 2011.
We plan to submit a revised
information collection request (ICR) to
OMB to address the reduction of burden
associated with the ‘‘hardship test’’ and
6-month ERS period. As discussed in
Section I. of the preamble, providers or
suppliers that meet the ‘‘hardship’’ test
and request only a 6-month ERS period,
will have the opportunity to pay back
the Medicare debt in 6 months without
having to submit financial
documentation to the contractor. This
new requirement reduces the
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information collection burden placed on
providers and suppliers. We will
announce the revisions to 0938–0270
under separate notice and comment
periods prior to submitting the revisions
for OMB approval.
VI. Regulatory Impact Statement
A. Overall Impact
We have examined the impacts of this
rule as required by Executive Order
12866 (September 1993, Regulatory
Planning and Review), the Regulatory
Flexibility Act (RFA) (September 19,
1980, Pub. L. 96–354), section 1102(b) of
the Social Security Act, the Unfunded
Mandates Reform Act of 1995 (Pub. L.
104–4), Executive Order 13132 on
Federalism, and the Congressional
Review Act (5 U.S.C. 804(2)).
Executive Order 12866 (as amended
by Executive Order 13258 directs
agencies to assess all costs and benefits
of available regulatory alternatives and,
if regulation is necessary, to select
regulatory approaches that maximize
net benefits (including potential
economic, environmental, public health
and safety effects, distributive impacts,
and equity). A regulatory impact
analysis (RIA) must be prepared for
major rules with economically
significant effects ($100 million or more
in any 1 year). This final rule will not
reach the economic threshold and thus
is not considered a major rule. There
will be no additional costs or
documented savings resulting from the
implementation of this final rule.
The RFA requires agencies to analyze
options for regulatory relief of small
businesses. For purposes of the RFA,
small entities include small businesses,
nonprofit organizations, and small
governmental jurisdictions. Most
hospitals and most other providers and
suppliers are small entities, either by
nonprofit status or by having revenues
of $6.5 million to $31.5 million in any
1 year. For purposes of the RFA,
approximately 95 percent of the health
care industry is considered small
businesses according to the Small
Business Administration’s size
standards with total revenues of $6.5
million to $31.5 million or less in any
1 year. Individuals and States are not
included in the definition of a small
entity. Because there are no additional
costs or documented savings resulting
from the implementation of this rule,
the Secretary has determined that this
final rule will not have a significant
economic impact on a substantial
number of small entities.
In addition, section 1102(b) of the Act
requires us to prepare a regulatory
impact analysis if a rule may have a
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significant impact on the operations of
a substantial number of small rural
hospitals. This analysis must conform to
the provisions of section 604 of the
RFA. For purposes of section 1102(b) of
the Act, we define a small rural hospital
as a hospital that is located outside of
a metropolitan statistical area and has
fewer than 100 beds. Because there are
no additional costs or documented
savings resulting from the
implementation of this final rule, this
final rule will not have a significant
impact on the operations of a substantial
number of small rural hospitals.
Section 202 of the Unfunded
Mandates Reform Act of 1995 also
requires that agencies assess anticipated
costs and benefits before issuing any
rule whose mandates require spending
in any 1 year of $100 million in 1995
dollars, updated annually for inflation.
That threshold level is currently
approximately $127 million. This final
rule will not impose spending costs on
State, local, or tribal governments in the
aggregate, or by the private sector, of
$127 million.
Executive Order 13132 establishes
certain requirements that an agency
must meet when it promulgates a
proposed rule (and subsequent final
rule) that imposes substantial direct
requirement costs on State and local
governments, preempts State law, or
otherwise has Federalism implications.
This final rule will not have a
substantial effect on State or local
governments.
B. Anticipated Effects
1. Effects on Medicare Providers and
Suppliers
implementation of this final rule. There
may be savings due to a possible
reduction in paperwork.
C. Alternatives Considered
We considered adopting
mathematically precise distinctions
between ‘‘hardship’’ and ‘‘extreme
hardship,’’ but rejected this approach.
To select any type of numerical
threshold, for example, defining
‘‘extreme hardship’’ as 15 percent of
total overpayments in an effort to
distinguish it from the test for
‘‘hardship,’’ will result in inequitable
outcomes for different providers and
suppliers as discussed in the ‘‘extreme
hardship’’ section in section II. of this
final rule, Provisions of the Proposed
Regulations.
In implementing section 935(a) of the
MMA, we want to assure providers and
suppliers that we will be looking closely
at the financial picture each of them has
that has prompted them to seek an ERS.
Analyzing these financial profiles is a
complex undertaking that does not lend
itself to overly simplified numerical
cutoffs that may qualify some for longer
repayment periods but deny them to
others that ought to be just as eligible.
We solicited comments on other
alternative ways to distinguish between
‘‘hardship’’ and ‘‘extreme hardship’’ in
an effort to establish a standardized
approach to applying the two
definitions.
D. Conclusion
In accordance with the provisions of
Executive Order 12866, this regulation
was reviewed by the Office of
Management and Budget.
This final rule could affect all
Medicare provider and supplier types
with a Medicare overpayment. This
final rule will allow Medicare providers
or suppliers falling within these
provisions a 6 month period to pay back
debt owed to Medicare without being
required to file extensive financial
documentation. We believe that this
short repayment time period could
provide a provider or supplier time to
generate or secure the necessary capital
to liquidate the debt without having to
file the financial documentation
required to secure a longer repayment
schedule.
List of Subjects in 42 CFR Part 401
Claims, Freedom of information,
Health facilities, Medicare, Privacy.
I For the reasons set forth in the
preamble, the Centers for Medicare &
Medicaid Services amends 42 CFR
chapter IV as set forth below:
2. Effects on Other Providers
Subpart F—Claims Collection and
Compromise
jlentini on PROD1PC65 with RULES
There will be no effect on other
providers.
PART 401—GENERAL
ADMINISTRATIVE REQUIREMENTS
1. The authority citation for part 401
is revised to read as follows:
I
Authority: Secs. 1102 and 1871 of the
Social Security Act (42 U.S.C. 1302 and
1395hh).
2. In § 401.601, paragraph (a) is
revised to read as follows:
I
3. Effects on the Medicare and Medicaid
Programs
§ 401.601
There will be no additional costs or
documented savings resulting from the
(a) Basis. This subpart implements the
following statutory provisions:
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Frm 00041
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36447
(1) For CMS the Debt Collection
Improvement Act of 1996 (Pub. L. 104–
134) (DCIA), 110 Stat. 1321, 1358 (April
26, 1996) (codified at 31 U.S.C. 3711),
and conforms to the regulations (31 CFR
parts 900–904) issued jointly by the
Department of the Treasury and the
Department of Justice that generally
prescribe claims collection standards
and procedures under the DCIA for the
Federal government.
(2) Section 1893(f)(1) of the Act
regarding the use of repayment plans.
*
*
*
*
*
I 3. In § 401.603, add a new definition
for ‘‘Extended repayment schedule’’ to
read as follows:
§ 401.603
Definitions.
*
*
*
*
*
Extended repayment schedule means
installment payments to pay back a
debt.
§ 401.607
[Amended]
4. In § 401.607—
A. Redesignate paragraph (c)(2) as
paragraph (c)(3).
I B. Add a new paragraph (c)(2).
The addition reads as follows:
I
I
§ 401.607
Claims collection.
*
*
*
*
*
(c) * * *
(2) Extended repayment schedule.
(i) For purposes of this paragraph
(c)(2), the following definitions apply:
Extreme hardship exists when a
provider or supplier qualifies as being
in ‘‘hardship’’ as defined in this
paragraph and the provider’s or
supplier’s request for an extended
repayment schedule (ERS) is approved
under paragraph (c)(3) of this section.
Hardship exists when the total
amount of all outstanding overpayments
(principal and interest) not included in
an approved, existing repayment
schedule is 10 percent or greater than
the total Medicare payments made for
the cost reporting period covered by the
most recently submitted cost report for
a provider filing a cost report, or for the
previous calendar year for a supplier or
non cost-report provider.
(ii) CMS or its contractor reviews a
provider’s or supplier’s request for an
ERS. For a provider or a supplier not
paid by Medicare during the previous
year or paid only during a portion of
that year, the contractor or CMS will use
the last 12 months of Medicare
payments. If less than a 12-month
payment history exists, the number of
months available is annualized to equal
an approximate yearly Medicare
payment level for the provider or
supplier.
(iii) For a provider or supplier
requesting an ERS, CMS or its contractor
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evaluates the request based on the
definitions and information submitted
under this paragraph (c)(2). For a
provider or supplier whose situation
does not meet the definitions in
paragraph (c)(2)(i) of this section, CMS
or its contractor evaluates the ERS
request using the information in
paragraph (c)(3) of this section in
deciding to grant an ERS.
(iv) CMS or its contractor is
prohibited from granting an ERS to a
provider or supplier if there is reason to
suspect the provider or supplier may
file for bankruptcy, cease to do business,
discontinue participation in the
Medicare program, or there is an
indication of fraud or abuse committed
against the Medicare program.
(v) CMS or its contractor may grant a
provider or a supplier an ERS of at least
6 months if repaying an overpayment
within 30 days will constitute a
‘‘hardship’’ as defined in paragraph
(c)(2)(i) of this section. If a provider or
supplier is granted an ERS under this
paragraph, missing one installment
payment constitutes a default and the
total balance of the overpayment will be
recovered immediately.
(vi) CMS or its contractor may grant
a provider or a supplier an ERS of 36
months and up to 60 months if repaying
an overpayment will constitute an
‘‘extreme hardship’’ as defined in
paragraph (c)(2)(i) of this section.
Authority: (Catalog of Federal Domestic
Assistance Program No. 93.773, Medicare—
Hospital Insurance; and Program No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
Dated: January 22, 2008.
Kerry Weems,
Acting Administrator, Centers for Medicare
& Medicaid Services.
Approved: February 27, 2008.
Michael O. Leavitt,
Secretary.
Editorial Note: This document was
received at the Office of the Federal Register
on June 11, 2008.
[FR Doc. E8–13520 Filed 6–26–08; 8:45 am]
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BILLING CODE 4120–01–P
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Jkt 214001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Parts 405, 424, and 498
[CMS–6003–F]
RIN 0938–AI49
Medicare Program; Appeals of CMS or
CMS Contractor Determinations When
a Provider or Supplier Fails to Meet the
Requirements for Medicare Billing
Privileges
Centers for Medicare and
Medicaid Services (CMS), HHS.
ACTION: Final rule.
AGENCY:
SUMMARY: This final rule implements a
number of regulatory provisions that are
applicable to all providers and
suppliers, including durable medical
equipment, prosthetics, orthotics, and
supplies (DMEPOS) suppliers. This final
rule establishes appeals processes for all
providers and suppliers whose
enrollment, reenrollment or revalidation
application for Medicare billing
privileges is denied and whose
Medicare billing privileges are revoked.
It also establishes timeframes for
deciding enrollment appeals by an
Administrative Law Judge (ALJ) within
the Department of Health and Human
Services (DHHS) or the Departmental
Appeals Board (DAB), or Board, within
the DHHS; and processing timeframes
for CMS’ Medicare fee-for-service (FFS)
contractors.
In addition, this final rule allows
Medicare FFS contractors to revoke
Medicare billing privileges when a
provider or supplier submits a claim or
claims for services that could not have
been furnished to a beneficiary. This
final rule also specifies that a Medicare
contractor may establish a Medicare
enrollment bar for any provider or
supplier whose billing privileges have
been revoked.
Lastly, the final rule requires that all
providers and suppliers receive
Medicare payments by electronic funds
transfer (EFT) if the provider or
supplier, is submitting an initial
enrollment application to Medicare,
changing their enrollment information,
revalidating or re-enrolling in the
Medicare program.
DATES: Effective Date: These regulations
are effective on August 26, 2008.
FOR FURTHER INFORMATION CONTACT:
August Nemec, (410) 786–0612.
SUPPLEMENTARY INFORMATION:
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I. Background
A Medicare beneficiary may obtain
covered Medicare items or services from
any person, or institution that is
enrolled in the Medicare program and is
qualified to furnish those services.
Various provisions of the statute and
regulations establish conditions of
participation or standards that a
healthcare provider or supplier must
meet in order to receive Medicare
payment. These standards differ
depending on the type of provider or
supplier involved and whether the
services are furnished under Parts A or
B of the Medicare statute. There are also
differences in qualifications between
providers and suppliers of services, and
differences among the various types of
suppliers, in how they are enrolled in
the Medicare program. For some
classifications of providers and
suppliers, an on-site survey is required.
For other individuals or entities, a
determination can be made based
largely on the information provided by
the applicant.
The Medicare regulations in 42 CFR
part 498 provide appeal rights for
providers and suppliers that have been
found to not meet certain conditions of
participation or established standards.
For the purposes of part 498, these
suppliers include, but are not limited to,
independent laboratories; suppliers of
portable x-ray services; rural health
clinics; federally qualified health
centers; ambulatory surgical centers;
entities approved by CMS to furnish
outpatient diabetes self-management
training or end-stage renal disease
treatment facilities. For the purposes of
part 498, the term ‘‘provider’’ refers to
a hospital, critical access hospital
(CAH), skilled nursing facility,
comprehensive outpatient rehabilitation
facility (CORF), home health agency or
hospice (HHA), religious nonmedical
health care institutions (RNHCIs) that
has in effect an agreement to participate
in Medicare; or a clinic, rehabilitation
agency, or public health agency that has
in effect a similar agreement but only to
furnish outpatient physical therapy or
speech pathology services.
In addition, § 405.874 provides an
appeals process for suppliers of
DMEPOS that wish to contest a denial
of an application for billing privileges or
the revocation of existing billing
privileges. It also affords DMEPOS
suppliers the right to a carrier or
Medicare Administrative Contractor
(MAC) hearing before an official who
was not involved in the original
determination, and the right to seek a
review before a CMS official designated
by the CMS Administrator.
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Agencies
[Federal Register Volume 73, Number 125 (Friday, June 27, 2008)]
[Rules and Regulations]
[Pages 36443-36448]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-13520]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 401
[CMS-6032-F]
RIN 0938-AO27
Medicare Program; Use of Repayment Plans
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This final rule modifies Medicare regulations to implement
section 935(a) of the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003 pertaining to the use of repayment plans
(also known as extended repayment schedules or ``ERS'') for Medicare
provider and supplier overpayments. Under this provision, we are
granting a provider or a supplier an ERS under certain terms and
conditions as defined in the statute. This final rule establishes
criteria and procedures to apply this requirement and to define the
concepts of ``hardship'' and ``extreme hardship.''
DATES: Effective Date: These regulations are effective on July 28,
2008.
FOR FURTHER INFORMATION CONTACT: Tom Noplock, (410) 786-3378.
SUPPLEMENTARY INFORMATION:
I. Background
A. Medicare Overpayment
Medicare overpayments are Medicare funds an individual, provider,
or supplier has received that exceed amounts due and payable under the
Medicare statute and regulations (plus any applicable interest and
penalties assessed on the overpayment). Section 400.202 defines a
``supplier'' as ``a physician or other practitioner, or an entity other
than a provider, that furnishes health care services under Medicare.''
Generally, overpayments result when payment is made by Medicare for
items or services that are not covered, exceeds the amount allowed by
Medicare for an item or service, or is made for items or services that
should have been paid by another insurer (for example, Medicare
secondary payer obligations). Once a determination and any necessary
adjustments in the amount of the overpayment have been made, the
remaining amount is a debt owed to the United States Government.
Section 1870 of the Social Security Act (the Act) provides a
framework within which liability for such Medicare overpayments is
determined and recoupment of overpayments is pursued. This framework
prescribes a decision making process that the agency follows when
pursuing the recoupment of Medicare overpayments.
The regulation governing the liability for Medicare overpayments is
located at 42 CFR part 401 (subpart F).
B. Statutory Authority
The Federal Claims Collection Act of 1966 (Pub. L. 89-508) (FCCA),
80 Stat. 308 (amended by the Debt Collection Improvement Act of 1996
(Pub. L. 104-134) (DCIA) (codified at 31 U.S.C. 3711)) is the Federal
government's basic statutory authority for debt management practices.
The Congress intended the FCCA to reduce the amount of litigation
previously required to collect claims and to reduce the volume of
private relief legislation in the Congress. The FCCA was intended to be
independent of the other authorities we use to collect debt and added
to, rather than supplanted, our other authorities, including common law
authority.
The FCCA authorized the head of an agency to collect claims in any
amount. This statute also provided that the head of an agency may,
under certain conditions, compromise a claim, or suspend or terminate
collection action on a claim. Uncollectible claims in excess of
$100,000, exclusive of interest, must be referred to the Department of
Justice for compromise. The FCCA was amended in 1996 and is now
referred to as the Debt Collection Improvement Act of 1996 (Pub. L.
104-134) (DCIA), 110 Stat. 1321, 1358 (April 26, 1996) (codified at 31
U.S.C. 3711).
In the November 2, 1977 Federal Register (42 FR 57351), the
Secretary of the Department of Health and Human Services (the
Secretary) published a rule to delegate authority to the Department
Claims Officer generally, and the Administrator of the Centers for
Medicare & Medicaid Services (the Administrator) for necessary claims
collection actions under our programs. The authority delegated to the
Administrator covers all of our activities in the Medicare program
(Title XVIII) and pertains to claims up to $20,000. (This amount has
been increased to $100,000; see 31 U.S.C. 3711.)
In the August 29, 1983 Federal Register (48 FR 39060), we published
the ``Federal Claims Collection Act; Claims Collection and Compromise''
final rule with comment period in accordance with the FCCA. In that
final rule with comment period, we adopted the applicable debt
collection tools made available to us under the FCCA including the
ability to collect or compromise claims, or suspend or terminate
collection action, as appropriate. The final rule with comment period
also set forth the requirements we use to evaluate debtors' requests
for extended repayment agreements specified in Sec. 401.607.
As part of the Health Insurance Portability and Accountability Act
of 1996 (Pub. L. 104-191) (HIPAA), the Congress added section 1893 to
the Act establishing the Medicare integrity program (MIP) to carry out
Medicare program integrity activities that are funded from the Medicare
Trust Funds. Section 1893 of the Act expands our contracting authority
to allow us to contract with eligible entities to perform MIP
activities. These activities include review of provider and supplier
activities including medical, fraud, and utilization review; cost
report audits; Medicare secondary payer determinations; education of
providers, suppliers, beneficiaries, and other persons regarding
payment integrity and benefit quality assurance issues; and developing
and updating a list of durable medical equipment items that are subject
to prior authorization (42 U.S.C. 1395ddd). These MIP contractors
assist us in the identification and collection of Medicare provider and
supplier overpayments.
[[Page 36444]]
C. Overview of Current Policy
The current policy that CMS and its contractors use for the
evaluation of extended repayment schedules (ERSs) is based on the
existing regulations at Sec. 401.607(c)(2) and guidance in the
Medicare Financial Management Manual, Pub. 100-6 (Chapter 4, Section
50). Under our current policy, we determine the frequency and amount of
the installment payments based on the factors set forth at the current
Sec. 401.607(c)(2) which include the following: (1) The amount of the
claim; (2) the debtor's ability to pay; and (3) the cost to CMS of
administering an installment agreement.
Under the current ERS review process, we primarily focus on the
second factor, the debtor's ability to repay the overpayment, by
conducting a review of the debtor's financial status, similar to how
banks assess applicants for a loan. In almost all cases, we try to work
with the provider or supplier to recover the overpayment. In general,
it has been our experience that it is in both CMS and the debtor's best
interests to work out a reasonable repayment schedule to recoup an
overpayment rather than demand immediate collection of the debt within
30 days, which could place a provider or supplier at financial risk or
bring the provider or supplier a step closer to bankruptcy.
Under our existing procedures we review financial documentation
submitted by the provider or supplier to assess the provider's or
supplier's ability to repay the Medicare overpayment. This
documentation must include, at a minimum, a statement of financial
position (for example, a balance sheet), a statement of financial
performance (for example, an income statement), and a statement of
future viability (for example, a projected statement of cash flow). In
addition, the provider must include a letter from a financial
institution proving that it cannot obtain financing from an alternative
source.
D. Medicare Prescription Drug, Improvement, and Modernization Act of
2003
On December 8, 2003, the Congress enacted the Medicare Prescription
Drug, Improvement, and Modernization Act of 2003 (Pub. L. 108-173)
(MMA). This legislation contained provisions affecting the recovery of
provider and supplier overpayments under the Medicare program. Section
935(a) of the MMA amended title XVIII of the Act by adding a new
section 1893(f)(1) to the Act to require us to use certain statutory
criteria in evaluating whether a provider or supplier should be granted
a repayment schedule of at least 6 months and up to 5 years.
II. Provisions of the Proposed Regulations
The following is an overview of the provisions we proposed in the
Use of Repayment Plans proposed rule published in the November 27, 2006
Federal Register (71 FR 68519).
1. Hardship Provision
Under section 1893(f)(1) of the Act, we may grant a provider or a
supplier upon request, a repayment schedule of at least 6 months, if
repaying an overpayment within 30 days would constitute a ``hardship''
on the provider or supplier, provided that certain criteria are met.
The new statute at section 1893(f)(1)(B)(i) of the Act defines
``hardship'' based on the relationship between the amount of the
Medicare overpayment(s) not covered under an existing ERS owed by a
provider or supplier and the total amount of Medicare payments made to
that provider or supplier over the most recently submitted cost report
or for the previous calendar year.
Under section 1893(f)(1)(B) of the Act, a provider or supplier's
repayment of an overpayment within 30 days is deemed to be a
``hardship'' when the total amount of all outstanding overpayments not
included in an approved existing repayment schedule is 10 percent or
greater than the total Medicare payments made for the cost reporting
period covered by the most recently submitted cost report (for a
provider filing a cost report), or the previous calendar year (for a
supplier or non cost report provider). We proposed to interpret
``outstanding overpayments'' to include both principal and accrued
interest. We read the newly added section 1893(f)(1)(B)(iii) of the Act
to exclude overpayments already being repaid under an approved ERS.
We proposed to interpret the new ``hardship'' test under section
935(a) of the MMA as not to supersede our ERS regulations currently at
Sec. 401.607(c)(2), (which we proposed to redesignate as Sec.
401.607(c)(3)). Since our existing regulations governing ERSs are
issued under the FCCA, we do not plan to eliminate the criteria and
procedures currently used to grant providers and suppliers ERSs.
Instead, we proposed to add an initial ``hardship'' test to existing
regulations and procedures for determining a debtor's ERS.
We proposed that all requests for an ERS first be evaluated under
the new ``hardship'' test. Under section 935(a) of the MMA, if
``hardship'' is determined and no statutory exception applies under
Sec. 401.607(c)(2)(iv), then the statute requires that the Secretary
grant a provider or supplier a repayment period of at least 6 months
but not longer than 3 years.
Section 935(a) of the MMA requires that the Secretary establish
rules for cases when a provider or a supplier was not paid during the
previous year or paid for only a portion of that year. For these cases,
we proposed to use the last 12 months of Medicare payments made to the
provider or supplier. In cases where there is less than a 12-month
payment history, we proposed that the number of months available be
annualized to equal an approximate yearly Medicare payment level for
the provider or supplier. (For detailed examples on how to apply the
new ``hardship'' test provided in section 1893(f)(1) of the Act, please
see the November 27, 2006 proposed rule, ``Use of Repayment Plans'' (71
FR 68521).)
2. Exceptions Under the ``Hardship'' Provision in Section 935(a) of the
MMA
Section 935(a) of the MMA sets out exceptions to granting a
provider or supplier an extended repayment schedule even if the
provider or supplier meets the ``hardship'' test. These exceptions
occur when there is reason to suspect the provider or supplier may file
for bankruptcy, cease to do business, discontinue participation in the
program, or when there is an indication of fraud or abuse committed
against the program. (We proposed that contractors continue to use
existing procedures and definitions applicable to bankruptcy and fraud
or abuse.) In such cases, CMS or its contractors are prohibited from
granting an ERS.
3. Extreme Hardship Provision
Under the provisions of Sec. 401.607(c)(2)(vi) of this final rule,
the Secretary may grant a provider or a supplier a repayment schedule
of 36 months and up to 60 months if repaying an overpayment would
constitute an ``extreme hardship'' unless a statutory exception applies
under Sec. 401.607(c)(2)(iv). Since the Congress left the definition
of ``extreme hardship'' to our discretion, we considered different
approaches for defining ``extreme hardship'' and sought public comment
on this section.
We considered proposing a new financial threshold to determine if a
provider or supplier was in extreme financial hardship, such as using a
15 percent threshold. We rejected this
[[Page 36445]]
approach because it could result in discriminating against providers
and suppliers who may be similarly financially situated but may
attribute more of their total revenue to Medicare income. This could
occur for example with a home health agency (HHA) which may attribute
100 percent of its revenue to Medicare business and a skilled nursing
facility (SNF) which may only attribute 20 percent of its business to
Medicare.
We proposed to define ``extreme hardship'' when a provider or
supplier qualifies under the ``hardship'' provision defined above and
the provider's or supplier's request for an ERS is approved under newly
redesignated Sec. 401.607(c)(3). If we determine the request meets the
criteria in the redesignated Sec. 401.607(c)(3) and meets the CMS
manual guidance set forth in the Medicare Financial Management Manual,
Pub. 100-6, Chapter 4, Section 50, we proposed that the provider or
supplier may be granted an ERS between 36 and 60 months. We also
proposed that contractors apply the statutory exceptions to ``extreme
hardship'' cases in a similar manner as they do to ``hardship'' cases.
We solicited comments on other alternative approaches to define
``extreme hardship'' that could distinguish between the most extreme
cases requiring ERSs between 36 and 60 months.
4. Extended Repayment Schedules (ERSs)
We proposed to initially handle ERS requests differently than we
have under our current regulations. We proposed to allow providers or
suppliers that meet the ``hardship'' test and request only a 6-month
ERS period, the opportunity to pay back the Medicare debt in 6 months
without having to submit financial documentation to the contractor in
accordance with the existing instructions in the Medicare Financial
Management Manual, CMS, Pub. 100-6, Chapter 4, Section 50. We believe
that by waiving the requirement to submit financial documentation (such
as financial statements or a bank denial letter) for a 6-month ERS, we
allow a provider or supplier time to generate or secure the necessary
capital to liquidate the debt without having to file extensive
documentation in order to secure a repayment schedule.
We therefore proposed that a provider or supplier that requests a
6-month ERS, meets the ``hardship'' test, does not fall within an
exception, and elects not to submit financial documentation would be
approved for a 6-month ERS. Any provider or supplier qualifying for the
6-month ERS under the ``hardship'' provision has the choice to turn
down the 6-month ERS and either pay off the debt within 30 days of the
date of determination or request a longer than 6-month ERS. In
addition, we proposed not to prohibit any provider or supplier under
the 6-month ``hardship'' provision ERS from applying for a longer ERS
if it later desires to do so under Sec. 401.607(c)(3).
For all ERS requests greater than 6 months, we proposed to rely on
current regulations and procedures that require the provider or
supplier to submit financial documentation in accordance with the
Medicare Financial Management Manual, CMS Pub. 100-6, Chapter 4,
Section 50. A provider or supplier must continue to submit a written
request that refers to the specific overpayment for which an ERS is
being requested, the number of months requested in the ERS, and include
the first payment with its request. The contractor would determine the
duration of the ERS based on its review of the provider or supplier's
documentation in accordance with CMS manual guidance.
If a provider or supplier misses one installment payment in any ERS
granted under section 935(a) of the MMA, the statute permits us to
immediately collect the entire overpayment. However, we proposed to
impose this penalty only on the ``automatic'' 6-month ERS. With all
other ERSs, we proposed to continue to use the existing procedures that
define a default of an ERS as missing two consecutive installment
payments.
We proposed to revise Sec. 401.601(a) to read as follows: ``This
subpart implements the following provisions: (1) For CMS the Debt
Collection Improvement Act of 1996 (Pub. L. 104-134) (DCIA), 110 Stat.
1321, 1358 (April 26, 1996) (codified at 31 U.S.C. 3711), and conforms
to the regulations (31 CFR parts 900-904) issued jointly by the
Department of the Treasury and the Department of Justice that generally
prescribe claims collection standards and procedures under the DCIA for
the Federal government; (2) section 1893(f)(1) of the Act regarding the
use of repayment plans.''
In addition, in Sec. 401.603 we proposed to add a definition for
an ``extended repayment schedule.''
We proposed to redesignate Sec. 401.607(c)(2) as Sec.
401.607(c)(3). In addition, we proposed a new Sec. 401.607(c)(2),
Extended repayment schedule, in accordance with section 1893(f)(1) of
the Act. We proposed to implement the provisions of section 1893(f)(1)
of the Act, as amended by section 935(a) of the MMA, in new Sec.
401.607(c)(2), Extended repayment schedule.
III. Analysis of and Responses to Public Comments
We received 6 public comments on the November 27, 2006 proposed
rule. The following is a summary of the major issues and our responses.
Comment: One commenter believed that the provisions of the proposed
rule were not equitable between provider types because 10 percent of
total Medicare reimbursement for a provider with a 50 percent Medicare
fee-for-service revenue is a greater threshold to reach than a provider
with a 5 percent Medicare fee-for-service revenue.
Response: We agree with the comment that the proposed rule may not
in all cases treat different provider types similarly. However, the
statute was written to define hardship as a ratio of Medicare
overpayments to total Medicare payments/reimbursement in a given time
period. The statute does not allow CMS to take into account the
percentage of patient revenue from other sources when defining
``hardship.'' For all other ERS requests, we proposed to rely on
current regulations and procedures that require the provider or
supplier to submit financial documentation in accordance with the
Medicare Financial Management Manual, CMS Pub. 100-6, Chapter 4,
Section 50.
Comment: Some commenters believed it would be more consistent and
more fair to providers if we would use the definition of default for
all ERSs as missing two consecutive installment payments.
Response: While the statute permits us to immediately collect on an
entire overpayment if a provider or supplier misses one installment
payment in any ERS granted under section 935(a) of the MMA, we have
decided to impose the 1-month missed payment rule only for the 6-month
``hardship-based'' ERS. We chose not to apply the two missed payment
rule to 6-month ERSs because we do not want a provider or supplier to
be too far in arrears if they miss payments in such a short ERS. A
provider or supplier that is behind two payments in a 6-month ERS has a
greater amount of its payments in arrears than a provider or supplier
that is behind two payments in a 36-month or 60-month ERS. For example,
two missed payments on the amortization of an overpayment covered under
a 6-month ERS (2 divided by 6) is equal to approximately 33.3 percent
of the total overpayment whereas 2 missed payments under a 36-month ERS
(2
[[Page 36446]]
divided by 36) is equal to a much lower 5.5 percent of the total
overpayment. On a 60-month ERS, two missed payments would only equal
3.3 percent of the total overpayment (2 divided by 60).
Comment: Some commenters were concerned that we may be
inadvertently legally binding providers to the ``automatic'' 6-month
ERS and not offering providers a future opportunity to request a second
ERS under Sec. 401.607(c).
Response: In the proposed rule, we stated that any provider or
supplier qualifying for the 6-month ERS under the ``hardship''
provision has the choice to turn down the 6-month ERS and either pay
off the debt within 30 days of the date of determination or request a
longer ERS under newly redesignated Sec. 401.607(c)(3). In addition,
we will not prohibit any provider or supplier under the 6-month
``hardship'' provision ERS from applying for a longer ERS if it later
desires to do so under Sec. 401.607(c)(3).
Comment: One commenter believed that there is no practical reason
for why we have not adopted a parallel numerical threshold approach to
extreme hardship by using some percentage above the numerical 10
percent threshold for hardship.
Response: The 10 percent used in this final rule to define hardship
is required by statute. As stated in the proposed rule, we considered
proposing a new financial threshold to determine if a provider or
supplier was in extreme financial hardship, such as using a 15 percent
threshold. However, we rejected this approach because it could result
in discriminating against providers and suppliers who may be similarly
financially situated but may attribute more of their total revenue to
Medicare income. This could occur for example with a home health agency
(HHA) which may attribute 100 percent of its revenue to Medicare
business and a skilled nursing facility (SNF) which may only attribute
20 percent of its business to Medicare. In addition, the ERS review
process is a multivariable financial analysis and it would not be
practical or equitable to either the provider/supplier or the Medicare
program to reduce the ERS process down to a single variable. We believe
keeping the definition of extreme hardship broader than a single
variable is in the best interests of the provider and supplier
community and is the most effective way to ensure that overpayments
will be collected and returned to the Medicare Trust Fund.
Comment: One commenter stated that there is confusion as to why the
burden of producing financial documentation can be removed for the
``automatic'' 6-month ERS but not for ERS plans longer than 6 months.
Response: We removed the financial documentation requirement for 6-
month ERSs because the contractor already has the requisite information
needed to determine if a provider or supplier meets the statutory
hardship test. However, in order to grant an ERS longer than 6 months,
we continue to need financial documentation to determine a provider or
supplier's ability to make future ERS payments. We also need financial
data to determine the length of the ERS or payback period that should
be granted to the provider or supplier. While a short ERS may cause a
provider or supplier to go out of business, the longer the ERS period
the greater the delay in the overpayment recovery and the greater the
financial risk to the Medicare program. We believe the increased risk
associated with a longer repayment or amortization period requires that
we give an ERS request greater financial scrutiny.
Comment: We received comments that were outside the scope of the
proposed rule (for example, regarding the effects on State Medicaid
programs).
Response: We are not responding in this final rule to comments that
are outside of the scope of the proposed rule.
IV. Provisions of the Final Regulations
As a result of our review of the public comments, we do not find
any cause to alter the provisions of the proposed rule. Therefore, we
are finalizing the provisions as proposed.
V. Collection of Information Requirements
This final rule does not impose any new information collection or
recordkeeping requirements. The information collection requirements
discussed in the preamble pertain to the extension of repayment
schedules. The requirements and associated paperwork burden are
approved under Office of Management and Budget (OMB) control number
0938-0270, with a current expiration date of January 31, 2011.
We plan to submit a revised information collection request (ICR) to
OMB to address the reduction of burden associated with the ``hardship
test'' and 6-month ERS period. As discussed in Section I. of the
preamble, providers or suppliers that meet the ``hardship'' test and
request only a 6-month ERS period, will have the opportunity to pay
back the Medicare debt in 6 months without having to submit financial
documentation to the contractor. This new requirement reduces the
information collection burden placed on providers and suppliers. We
will announce the revisions to 0938-0270 under separate notice and
comment periods prior to submitting the revisions for OMB approval.
VI. Regulatory Impact Statement
A. Overall Impact
We have examined the impacts of this rule as required by Executive
Order 12866 (September 1993, Regulatory Planning and Review), the
Regulatory Flexibility Act (RFA) (September 19, 1980, Pub. L. 96-354),
section 1102(b) of the Social Security Act, the Unfunded Mandates
Reform Act of 1995 (Pub. L. 104-4), Executive Order 13132 on
Federalism, and the Congressional Review Act (5 U.S.C. 804(2)).
Executive Order 12866 (as amended by Executive Order 13258 directs
agencies to assess all costs and benefits of available regulatory
alternatives and, if regulation is necessary, to select regulatory
approaches that maximize net benefits (including potential economic,
environmental, public health and safety effects, distributive impacts,
and equity). A regulatory impact analysis (RIA) must be prepared for
major rules with economically significant effects ($100 million or more
in any 1 year). This final rule will not reach the economic threshold
and thus is not considered a major rule. There will be no additional
costs or documented savings resulting from the implementation of this
final rule.
The RFA requires agencies to analyze options for regulatory relief
of small businesses. For purposes of the RFA, small entities include
small businesses, nonprofit organizations, and small governmental
jurisdictions. Most hospitals and most other providers and suppliers
are small entities, either by nonprofit status or by having revenues of
$6.5 million to $31.5 million in any 1 year. For purposes of the RFA,
approximately 95 percent of the health care industry is considered
small businesses according to the Small Business Administration's size
standards with total revenues of $6.5 million to $31.5 million or less
in any 1 year. Individuals and States are not included in the
definition of a small entity. Because there are no additional costs or
documented savings resulting from the implementation of this rule, the
Secretary has determined that this final rule will not have a
significant economic impact on a substantial number of small entities.
In addition, section 1102(b) of the Act requires us to prepare a
regulatory impact analysis if a rule may have a
[[Page 36447]]
significant impact on the operations of a substantial number of small
rural hospitals. This analysis must conform to the provisions of
section 604 of the RFA. For purposes of section 1102(b) of the Act, we
define a small rural hospital as a hospital that is located outside of
a metropolitan statistical area and has fewer than 100 beds. Because
there are no additional costs or documented savings resulting from the
implementation of this final rule, this final rule will not have a
significant impact on the operations of a substantial number of small
rural hospitals.
Section 202 of the Unfunded Mandates Reform Act of 1995 also
requires that agencies assess anticipated costs and benefits before
issuing any rule whose mandates require spending in any 1 year of $100
million in 1995 dollars, updated annually for inflation. That threshold
level is currently approximately $127 million. This final rule will not
impose spending costs on State, local, or tribal governments in the
aggregate, or by the private sector, of $127 million.
Executive Order 13132 establishes certain requirements that an
agency must meet when it promulgates a proposed rule (and subsequent
final rule) that imposes substantial direct requirement costs on State
and local governments, preempts State law, or otherwise has Federalism
implications. This final rule will not have a substantial effect on
State or local governments.
B. Anticipated Effects
1. Effects on Medicare Providers and Suppliers
This final rule could affect all Medicare provider and supplier
types with a Medicare overpayment. This final rule will allow Medicare
providers or suppliers falling within these provisions a 6 month period
to pay back debt owed to Medicare without being required to file
extensive financial documentation. We believe that this short repayment
time period could provide a provider or supplier time to generate or
secure the necessary capital to liquidate the debt without having to
file the financial documentation required to secure a longer repayment
schedule.
2. Effects on Other Providers
There will be no effect on other providers.
3. Effects on the Medicare and Medicaid Programs
There will be no additional costs or documented savings resulting
from the implementation of this final rule. There may be savings due to
a possible reduction in paperwork.
C. Alternatives Considered
We considered adopting mathematically precise distinctions between
``hardship'' and ``extreme hardship,'' but rejected this approach. To
select any type of numerical threshold, for example, defining ``extreme
hardship'' as 15 percent of total overpayments in an effort to
distinguish it from the test for ``hardship,'' will result in
inequitable outcomes for different providers and suppliers as discussed
in the ``extreme hardship'' section in section II. of this final rule,
Provisions of the Proposed Regulations.
In implementing section 935(a) of the MMA, we want to assure
providers and suppliers that we will be looking closely at the
financial picture each of them has that has prompted them to seek an
ERS. Analyzing these financial profiles is a complex undertaking that
does not lend itself to overly simplified numerical cutoffs that may
qualify some for longer repayment periods but deny them to others that
ought to be just as eligible. We solicited comments on other
alternative ways to distinguish between ``hardship'' and ``extreme
hardship'' in an effort to establish a standardized approach to
applying the two definitions.
D. Conclusion
In accordance with the provisions of Executive Order 12866, this
regulation was reviewed by the Office of Management and Budget.
List of Subjects in 42 CFR Part 401
Claims, Freedom of information, Health facilities, Medicare,
Privacy.
0
For the reasons set forth in the preamble, the Centers for Medicare &
Medicaid Services amends 42 CFR chapter IV as set forth below:
PART 401--GENERAL ADMINISTRATIVE REQUIREMENTS
0
1. The authority citation for part 401 is revised to read as follows:
Authority: Secs. 1102 and 1871 of the Social Security Act (42
U.S.C. 1302 and 1395hh).
Subpart F--Claims Collection and Compromise
0
2. In Sec. 401.601, paragraph (a) is revised to read as follows:
Sec. 401.601 Basis and scope.
(a) Basis. This subpart implements the following statutory
provisions:
(1) For CMS the Debt Collection Improvement Act of 1996 (Pub. L.
104-134) (DCIA), 110 Stat. 1321, 1358 (April 26, 1996) (codified at 31
U.S.C. 3711), and conforms to the regulations (31 CFR parts 900-904)
issued jointly by the Department of the Treasury and the Department of
Justice that generally prescribe claims collection standards and
procedures under the DCIA for the Federal government.
(2) Section 1893(f)(1) of the Act regarding the use of repayment
plans.
* * * * *
0
3. In Sec. 401.603, add a new definition for ``Extended repayment
schedule'' to read as follows:
Sec. 401.603 Definitions.
* * * * *
Extended repayment schedule means installment payments to pay back
a debt.
Sec. 401.607 [Amended]
0
4. In Sec. 401.607--
0
A. Redesignate paragraph (c)(2) as paragraph (c)(3).
0
B. Add a new paragraph (c)(2).
The addition reads as follows:
Sec. 401.607 Claims collection.
* * * * *
(c) * * *
(2) Extended repayment schedule.
(i) For purposes of this paragraph (c)(2), the following
definitions apply:
Extreme hardship exists when a provider or supplier qualifies as
being in ``hardship'' as defined in this paragraph and the provider's
or supplier's request for an extended repayment schedule (ERS) is
approved under paragraph (c)(3) of this section.
Hardship exists when the total amount of all outstanding
overpayments (principal and interest) not included in an approved,
existing repayment schedule is 10 percent or greater than the total
Medicare payments made for the cost reporting period covered by the
most recently submitted cost report for a provider filing a cost
report, or for the previous calendar year for a supplier or non cost-
report provider.
(ii) CMS or its contractor reviews a provider's or supplier's
request for an ERS. For a provider or a supplier not paid by Medicare
during the previous year or paid only during a portion of that year,
the contractor or CMS will use the last 12 months of Medicare payments.
If less than a 12-month payment history exists, the number of months
available is annualized to equal an approximate yearly Medicare payment
level for the provider or supplier.
(iii) For a provider or supplier requesting an ERS, CMS or its
contractor
[[Page 36448]]
evaluates the request based on the definitions and information
submitted under this paragraph (c)(2). For a provider or supplier whose
situation does not meet the definitions in paragraph (c)(2)(i) of this
section, CMS or its contractor evaluates the ERS request using the
information in paragraph (c)(3) of this section in deciding to grant an
ERS.
(iv) CMS or its contractor is prohibited from granting an ERS to a
provider or supplier if there is reason to suspect the provider or
supplier may file for bankruptcy, cease to do business, discontinue
participation in the Medicare program, or there is an indication of
fraud or abuse committed against the Medicare program.
(v) CMS or its contractor may grant a provider or a supplier an ERS
of at least 6 months if repaying an overpayment within 30 days will
constitute a ``hardship'' as defined in paragraph (c)(2)(i) of this
section. If a provider or supplier is granted an ERS under this
paragraph, missing one installment payment constitutes a default and
the total balance of the overpayment will be recovered immediately.
(vi) CMS or its contractor may grant a provider or a supplier an
ERS of 36 months and up to 60 months if repaying an overpayment will
constitute an ``extreme hardship'' as defined in paragraph (c)(2)(i) of
this section.
Authority: (Catalog of Federal Domestic Assistance Program No.
93.773, Medicare--Hospital Insurance; and Program No. 93.774,
Medicare--Supplementary Medical Insurance Program)
Dated: January 22, 2008.
Kerry Weems,
Acting Administrator, Centers for Medicare & Medicaid Services.
Approved: February 27, 2008.
Michael O. Leavitt,
Secretary.
Editorial Note: This document was received at the Office of the
Federal Register on June 11, 2008.
[FR Doc. E8-13520 Filed 6-26-08; 8:45 am]
BILLING CODE 4120-01-P