Medicaid Program and Children's Health Insurance Program (CHIP); Revisions to the Medicaid Eligibility Quality Control and Payment Error Rate Measurement Programs, 34468-34487 [E9-16538]
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Federal Register / Vol. 74, No. 134 / Wednesday, July 15, 2009 / Proposed Rules
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Parts 431, 447, and 457
[CMS–6150–P]
RIN 0938–AP69
Medicaid Program and Children’s
Health Insurance Program (CHIP);
Revisions to the Medicaid Eligibility
Quality Control and Payment Error
Rate Measurement Programs
srobinson on DSKHWCL6B1PROD with PROPOSALS3
AGENCY: Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
SUMMARY: This proposed rule would
implement provisions from the
Children’s Health Insurance Program
Reauthorization Act of 2009 (CHIPRA)
(Pub. L. 111–3) with regard to the
Medicaid Eligibility Quality Control
(MEQC) and Payment Error Rate
Measurement (PERM) programs. This
proposed rule would also codify several
procedural aspects of the process for
estimating improper payments in
Medicaid and the Children’s Health
Insurance Program (CHIP).
DATES: To be assured consideration,
comments must be received at one of
the addresses provided below, no later
than 5 p.m. on August 14, 2009.
ADDRESSES: In commenting, please refer
to file code CMS–6150–P. Because of
staff and resource limitations, we cannot
accept comments by facsimile (FAX)
transmission.
You may submit comments in one of
four ways (please choose only one of the
ways listed):
1. Electronically. You may submit
electronic comments on this regulation
to https://www.regulations.gov. Follow
the instructions for ‘‘Comment or
Submission’’ and enter the filecode to
find the document accepting comments.
2. By regular mail. You may mail
written comments (one original and two
copies) to the following address only:
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, Attention: CMS–
6150–P, P.O. Box 8020, Baltimore,
MD 21244–8020.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments (one
original and two copies) to the following
address only:
Centers for Medicare & Medicaid
Services, Department of Health and
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Human Services, Attention: CMS–
6150–P, Mail Stop C4–26–05, 7500
Security Boulevard, Baltimore, MD
21244–1850.
4. By hand or courier. If you prefer,
you may deliver (by hand or courier)
your written comments (one original
and two copies) before the close of the
comment period to either of the
following addresses:
a. Room 445–G, Hubert H. Humphrey
Building, 200 Independence Avenue,
SW., Washington, DC 20201.
(Because access to the interior of the
Hubert H. Humphrey (HHH) Building is
not readily available to persons without
Federal Government identification,
commenters are encouraged to leave
their comments in the CMS drop slots
located in the main lobby of the
building. A stamp-in clock is available
for persons wishing to retain a proof of
filing by stamping in and retaining an
extra copy of the comments being filed.)
b. 7500 Security Boulevard, Baltimore,
MD 21244–1850.
If you intend to deliver your
comments to the Baltimore address,
please call (410) 786–9994 in advance to
schedule your arrival with one of our
staff members.
Comments mailed to the addresses
indicated as appropriate for hand or
courier delivery may be delayed and
received after the comment period.
Submission of comments on
paperwork requirements. You may
submit comments on this document’s
paperwork requirements by following
the instructions at the end of the
‘‘Collection of Information
Requirements’’ section in this
document.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT:
Elizabeth Lindner, (410) 786–7481, or
Jessica Woodard, (410) 786–9249.
SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following Web
site as soon as possible after they have
been received: https://
www.regulations.gov. Follow the search
instructions on that Web site to view
public comments.
Comments received timely will also
be available for public inspection as
they are received, generally beginning
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approximately 3 weeks after publication
of a document, at the headquarters of
the Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday
through Friday of each week from 8:30
a.m. to 4 p.m. To schedule an
appointment to view public comments,
phone 1–800–743–3951.
I. Background
A. Medicaid Eligibility Quality Control
Program
The Medicaid Eligibility Quality
Control (MEQC) program is set forth in
section 1903(u) of the Social Security
Act (the Act) and requires States to
report to the Secretary the ratio of
States’ erroneous excess payments for
medical assistance to total expenditures
for medical assistance. Section 1903(u)
of the Act also sets a 3-percent threshold
for improper payments in any fiscal year
and the Secretary may withhold
payments to States based on the amount
of improper payments that exceed the
threshold.
B. The Improper Payments Information
Act of 2002
The Improper Payments Information
Act of 2002 (IPIA) (Pub. L. 107–300,
enacted on November 26, 2002) requires
the heads of Federal agencies to
annually review programs they oversee
to determine if they are susceptible to
significant erroneous payments. If any
programs are found to be susceptible to
significant improper payments, then the
agency must estimate the amount of
improper payments, report those
estimates to the Congress, and submit a
report on actions the agency is taking to
reduce erroneous expenditures. The
IPIA directed the Office of Management
and Budget (OMB) to provide guidance
on implementation. OMB defines
‘‘significant erroneous payments’’ as
annual erroneous payments in the
program exceeding both 2.5 percent of
program payments and $10 million
(OMB M–06–23, Appendix C to OMB
Circular A–123, August 10, 2006). For
those programs found to be susceptible
to significant erroneous payments,
Federal agencies must provide the
estimated amount of improper payments
and report on what actions the agency
is taking to reduce them, including
setting targets for future erroneous
payment levels and a timeline by which
the targets will be reached.
The Medicaid program and the
Children’s Health Insurance Program
(CHIP) were identified as programs at
risk for significant erroneous payments.
The Department of Health and Human
Services (DHHS) reports the estimated
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error rates for the Medicaid and CHIP
programs in its annual Performance and
Accountability Report (PAR) to
Congress.
C. Regulatory History
1. Medicaid Eligibility Quality Control
Program
Sections 431.800 through 431.865 set
forth the regulatory requirements for
States to conduct the annual MEQC
measurement. A Medicaid State
Operations letter (#93–58) dated July 23,
1993 implemented MEQC pilots that
allowed States to conduct special
studies that would take the place of the
‘‘traditional’’ MEQC review. States
conducting pilot reviews are not subject
to the threshold and disallowance
provisions under section 1903(u) of the
Act as long as the special studies
continue.
Currently, the MEQC program
consists of the following:
• MEQC traditional—Operating
MEQC under 42 CFR 431.800 through
431.865 and selecting a random sample
of all Medicaid applicants and enrollees
and reviewing them under guidance in
the State Medicaid Manual.
• MEQC pilots—Operating MEQC
under a special study, a target
population and providing oversight to
reduce and prevent errors and improve
program administration.
• MEQC waivers—Operating MEQC
as a part of a CMS approved section
1115 waiver and reviewing beneficiaries
included in the research and
demonstration project.
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2. Payment Error Rate Measurement
(PERM) Program
Section 1102(a) of the Act authorizes
the Secretary to establish such rules and
regulations as may be necessary for the
efficient administration of the Medicaid
and CHIP programs. The Medicaid
statute at section 1902(a)(6) of the Act
and the CHIP statute at section
2107(b)(1) of the Act require States to
provide information that the Secretary
finds necessary for the administration,
evaluation, and verification of the
States’ programs. Also, section
1902(a)(27) of the Act (and § 457.950 of
the regulations) requires providers to
submit information regarding payments
and claims as requested by the
Secretary, State agency, or both. Under
the authority of these statutory
provisions, we published in the August
27, 2004 Federal Register (69 FR 52620)
a proposed rule to comply with the
requirements of the IPIA and the OMB
guidance. The proposed rule set forth
provisions for all States to annually
estimate improper payments in their
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Medicaid and CHIP programs and to
report the State-specific error rates for
purposes of our computing the national
improper payment estimates for these
programs.
In the October 5, 2005 Federal
Register (70 FR 58260), we published an
interim final rule with comment period
(IFC). The IFC responded to public
comments on the proposed rule, and
informed the public of our national
contracting strategy and of our plan to
measure improper payments in a subset
of States. Our State selection process
ensures that a State is measured once,
and only once, every 3 years for each
program.
In response to the public comments
from the October 5, 2005 IFC, we
published a second IFC in the August
28, 2006 Federal Register (71 FR
51050), which reiterated our national
contracting strategy to estimate
improper payments in both Medicaid
and CHIP fee-for-service (FFS) and
managed care, and set forth and invited
further comments on State requirements
for estimating improper payments due
to errors in Medicaid and CHIP
eligibility determinations. We also
announced that a State’s Medicaid and
CHIP programs would be reviewed in
the same year.
In the August 31, 2007 Federal
Register (72 FR 50490), we published a
final rule for the PERM program, which
implements the IPIA requirements. The
August 31, 2007 final rule responded to
the public comments on the August 28,
2006 IFC and finalized State
requirements for submitting claims to
the Federal contractors that conduct
FFS and managed care reviews. The
final rule also finalized State
requirements for conducting eligibility
reviews and estimating payment error
rates due to errors in eligibility
determinations.
D. Children’s Health Insurance Program
Reauthorization Act of 2009
On February 4, 2009, the Children’s
Health Insurance Program
Reauthorization Act of 2009 (CHIPRA)
(Pub. L. 111–3) was enacted. (Please
note, as a result of this legislation, that
the program formerly known as the
‘‘State Children’s Health Insurance
Program (SCHIP)’’ is now referred to as
the ‘‘Children’s Health Insurance
Program (CHIP)’’). Sections 203 and 601
of the CHIPRA relate to the PERM
program.
Section 203 of the CHIPRA establishes
an error rate measurement with respect
to the enrollment of children under the
express lane eligibility option. The law
directs States not to include children
enrolled using the express lane
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eligibility option in data or samples
used for purposes of complying with the
MEQC and PERM requirements.
Provisions for States’ express lane
eligibility option will be set forth in a
future rulemaking document.
Section 601 of the CHIPRA provides
for a 90 percent Federal match for
Children’s Health Insurance Program
(CHIP) spending related to PERM
administration and excludes such
spending from the 10 percent
administrative cap. (Section 2105(c)(2)
of the CHIP statute gives States the
ability to use an amount up to 10
percent of the CHIP benefit
expenditures for outreach efforts,
additional services other than the
standard benefit package for low-income
children, and administrative costs.)
The CHIPRA requires a new PERM
rule and delays any calculation of a
PERM error rate for CHIP until 6 months
after the new PERM rule is effective.
Additionally, the CHIPRA provides that
States that were scheduled for PERM
measurement in fiscal year (FY) 2007
may elect to accept a CHIP PERM error
rate determined in whole or in part on
the basis of data for FY 2007, or may
elect instead to consider its PERM
measurement conducted for FY 2010 as
the first fiscal year for which PERM
applies to the State for CHIP. Similarly,
the CHIPRA provides that States that
were scheduled for PERM measurement
in FY 2008 may elect to accept a CHIP
PERM error rate determined in whole or
in part on the basis of data for FY 2008,
or may elect instead to consider its
PERM measurement conducted for FY
2011 as the first fiscal year for which
PERM applies to the State for CHIP.
The CHIPRA requires that the new
PERM rule include the following:
• Clearly defined criteria for errors for
both States and providers.
• Clearly defined processes for
appealing error determinations.
• Clearly defined responsibilities and
deadlines for States in implementing
any corrective action plans.
• Requirements for State verification
of an applicant’s self-declaration or selfcertification of eligibility for, and
correct amount of, medical assistance
under Medicaid or child health
assistance under CHIP.
• State-specific sample sizes for
application of the PERM requirements.
In addition, the CHIPRA aims to
harmonize the PERM and MEQC
programs and provides States with the
option to apply PERM data resulting
from its eligibility reviews for meeting
MEQC requirements and vice versa,
with certain conditions.
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E. CMS Response to the CHIPRA
As required by the CHIPRA, we are
proposing revised MEQC and PERM
provisions in this proposed rule.
Section 601(b) of the CHIPRA states
that ‘‘the Secretary shall not calculate or
publish any national or State-specific
error rate based on the application of the
payment error rate measurement (in this
section referred to as ‘PERM’)
requirements to CHIP until after the date
that is 6 months after the date on which
a new final rule (in this section referred
to as the ‘new final rule’) promulgated
after the date of the enactment of this
Act and implementing such
requirements in accordance with the
requirements of subsection (c) is in
effect for all States.’’ The CHIP error rate
for the FY 2008 cycle was scheduled to
be published in the FY 2009 PAR (in
November 2009), which is less than 6
months after the expected promulgation
and effective date of this new final rule.
Therefore, the publication of any CHIP
error rates for FY 2008 is delayed until
at least 6 months after the final rule
implementing the CHIPRA requirements
for PERM is effective.
As noted above, section 601(d) of the
CHIPRA provides that States that were
scheduled for PERM measurement in FY
2007 may elect to accept a CHIP PERM
error rate determined in whole or in part
on the basis of data for FY 2007, or may
elect instead to consider its PERM
measurement conducted for FY 2010 as
the first fiscal year for which PERM
applies to the State for CHIP. In
addition, the CHIPRA provides that
States that were scheduled for PERM
measurement in FY 2008 may elect to
accept a CHIP PERM error rate
determined in whole or in part on the
basis of data for FY 2008, or may elect
instead to consider its PERM
measurement conducted for FY 2011 as
the first fiscal year for which PERM
applies to the State for CHIP.
Accordingly, a State measured in the
FY 2007 cycle that elects to accept the
PERM error rate for its CHIP program
determined in whole or in part on the
basis of data for FY 2007 is required to
notify CMS of its intentions through an
acceptance form provided to all States
in a State Health Official letter.
Similarly, a State measured in the FY
2008 cycle that elects to accept the
PERM error rate for its CHIP program
determined in whole or in part on the
basis of data for FY 2008 is required to
notify CMS of its intentions through an
acceptance form provided to all States
in a State Health Official letter. If a State
measured in the FY 2007 or FY 2008
cycles elects to reject the CHIP PERM
rate determined during those cycles,
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they do not need to notify CMS of this
decision. However, information from
those cycles will not be used to
calculate the State-specific sample sizes
and CMS will rely on the standard
assumptions for determining sample
size.
In order for section 601(d) of the
CHIPRA to be read in harmony with the
IPIA, which requires a CHIP PERM error
rate to be calculated annually, we
believe that the appropriate reading of
section 601(d) of the CHIPRA,
construing the law as a whole and
giving effect to all language of the
CHIPRA, is that a State may only elect
to reject the PERM error rate for the
State’s CHIP program for FY 2007 or FY
2008 and instead have its PERM error
rate for its CHIP program measured in
FY 2010 or FY 2011, respectively. A
State scheduled for PERM measurement
in FY 2008 will still have its PERM error
rate for its Medicaid program measured.
Additionally, States scheduled for
PERM measurement in FY 2009 will
have the CHIP program reviewed and
error rates calculated after the final rule
is in effect. Furthermore, the FY 2009
Medicaid measurement is proceeding
with no delays as a result of the
CHIPRA, and FY 2009 Medicaid error
rates will be calculated under the new
final rule.
II. Provisions of the Proposed
Regulations
As a result of the CHIPRA, we are
proposing a nomenclature change to
parts 431, 447, and 457. The program
formerly known as the ‘‘State Children’s
Health Insurance Program (SCHIP)’’ is
now referred to as the ‘‘Children’s
Health Insurance Program (CHIP).’’ We
are also proposing the following
revisions to the current PERM
provisions:
A. Sample Sizes
Section 601(f) of the CHIPRA requires
us to establish State-specific sample
sizes for application of the PERM
requirements with respect to CHIP for
fiscal years beginning with the first
fiscal year that begins on or after the
date on which the new final rule is in
effect for all States, on the basis of such
information as the Secretary determines
appropriate. In establishing such sample
sizes, the Secretary shall, to the greatest
extent practicable: (1) Minimize the
administrative cost burden on States
under Medicaid and CHIP; and (2)
maintain State flexibility to manage
such programs.
To comply with the IPIA, the PERM
program must estimate a national
Medicaid and a national CHIP error rate
that covers the 50 States and District of
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Columbia. Consistent with OMB’s
precision requirements defined in its
IPIA guidance, the estimated national
error rate for each program must be
bound by a 90 percent confidence
interval of 2.5 percentage points in
either direction of the estimate. Since
States administer Medicaid and CHIP
and make payments for services
rendered under the programs, we collect
State-level information at a high level of
confidence (the estimated error rate for
a State must be bound by a 95 percent
confidence interval of 3 percentage
points in either direction). To estimate
the national error rate, as well as Statespecific error rates, reviews are
conducted in three areas for both the
Medicaid and CHIP programs: (1) Feefor-service (FFS), (2) managed care, and
(3) program eligibility. The FFS and
managed care reviews are referred to
jointly as the ‘‘claims review,’’ while the
program eligibility review is referred to
as the ‘‘eligibility review.’’
Samples of payments made on a FFS
and managed care basis for the claims
review and samples of beneficiaries for
the eligibility review are drawn each
year in order to calculate a national
error rate that meets the precision
requirements described in OMB
Guidance (OMB M–06–23, Appendix C
to OMB Circular A–123, August 10,
2006). The preferred method is to
achieve the precision goal with the
smallest sample size possible, so as to
reduce the staff burden on States, the
Federal government, beneficiaries, and
providers. We determined that the most
efficient method, statistically, is to draw
a sample of States and then draw a
sample of payments from the payments
made by the sampled States. The
process for drawing a sample of States
is described in detail in the preamble to
the August 31, 2007 final rule (72 FR
50490). We are not proposing
modifications to the current approach,
which samples 17 States per year for a
PERM measurement cycle. This
rulemaking addresses the State-specific
sample sizes for samples of claims and
beneficiaries within a State.
In light of the new CHIPRA
requirements, we are proposing to add
new § 431.972, to describe more fully
the claims sampling procedures used for
the claims review, as well as the process
for establishing State-specific sample
sizes for PERM, although we note that
the execution of these responsibilities
would remain with CMS and the
Federal contractors, not with the States.
Under the Secretary’s authority at
section 1102(a) of the Act and in order
to effectively implement the IPIA, we
are also proposing that these sampling
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procedures apply to both Medicaid and
CHIP.
We are also proposing to revise
§ 431.978 to provide additional
guidance on State Medicaid and CHIP
eligibility sample sizes by clarifying the
process for establishing State-specific
sample sizes.
are proposing that States must establish
controls to ensure that the FFS,
managed care, and eligibility universes
are complete and accurate. For example,
this would include the comparisons
between the PERM universes and the
State’s CMS–64 and CMS–21 financial
reports.
1. Fee-for-Service (FFS) and Managed
Care
b. Stratification
In FY 2006, we measured only the
error rate for the FFS component of
Medicaid. To obtain the required
precision levels while minimizing the
sample size, and therefore reducing the
burden on States, the claims universe
for FFS payments for Medicaid was
stratified by service category and a
stratified random sample was drawn for
each State. In FY 2007 and beyond, we
measure the error rates for Medicaid
FFS, Medicaid managed care, CHIP FFS,
and CHIP managed care separately (to
the extent that a State has each of these
programs). We also stratify each
universe by dollars rather than service
category.
Under this stratification and sampling
approach, all payments in each universe
are sorted from largest to smallest
payment amounts. The payments are
then divided into strata such that the
total payments in each stratum are the
same. For example, if five strata are
used, the total dollars in each stratum
would equal 20 percent of the total
dollars in the universe. The first stratum
would contain the highest dollar-valued
payments, and the last stratum would
contain the smallest dollar-valued
payments, including all zero-paid and
denied claims (denials have a zero
dollar amount, and therefore, would
appear in the stratum with the smallest
dollar values). An equal number of FFS
claims or managed care payments are
then drawn from each stratum, which
means the sample would include
proportionately more high-dollar
payments and proportionately fewer
low-dollar payments and denials,
compared to their representation in the
universe. This overweighting of higherdollar payments (which is taken into
account when calculating error rates)
enables us to draw a smaller sample size
that has a reasonable probability of
meeting the precision requirements,
compared to a perfectly random sample
or a sample stratified by service type. In
this manner, we reduce burden on
States, the Federal government,
beneficiaries, and providers.
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a. Universe Definition
In order to implement the IPIA and
related requirements (OMB M–06–23,
Appendix C to OMB Circular A–123,
August 10, 2006) that require Federal
agencies to estimate the amount of
improper payments in programs with
significant erroneous payments (which
includes Medicaid and CHIP), in the
current § 431.970(a)(1) we require States
to submit ‘‘[a]ll adjudicated fee-forservice (FFS) and managed care claims
information, on a quarterly basis, from
the review year,’’ so that a sample of
payments can be reviewed and from the
review findings CMS can estimate the
amount of improper payments in each
program. We propose to remove the
word ‘‘all’’ from § 431.970(a)(1) because
certain types of payments are excluded
from PERM sampling and review for
technical reasons. This requirement has
been further clarified through
instructions issued by CMS to the
States.
For the PERM claims review
component, the ‘‘claims universe’’ is
defined in the new § 431.972 as
including payments that were originally
paid (paid claims) and for which
payment was requested but denied
(denied claims) during the Federal fiscal
year, and for which there was Federal
financial participation (FFP) (or would
have been if the claim had not been
denied) through Title XIX of the Act
(Medicaid) or Title XXI of the Act
(CHIP). Depending on the context in
which it is used, the claims universe
may refer to either all of the adjudicated
FFS claims during the fiscal year under
review, or all of the managed care
capitation payments made during the
fiscal year under review, for Medicaid
or CHIP.
Due to the significant variation in
State systems for processing, paying,
and claiming reimbursement for
medical services under Medicaid and
CHIP, we are not proposing to include
a more specific claims universe
description in regulation. Rather, States
should refer to more detailed claims
universe specifications that will be
published by CMS in separate
instructions at the beginning of each
PERM measurement cycle. However, we
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c. Fee-for-Service and Managed Care
Sample Size
In order to establish State-specific
sample sizes, we are proposing that the
annual sample size in a State’s first
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PERM cycle (referred to as ‘‘initial
sample’’ or ‘‘base sample’’) would be
500 FFS claims and 250 managed care
payments.
We determined this initial sample
size based on the experience of the
PERM pilot study and our requirement
that the estimated error rate for a State
must be bound by a 95 percent
confidence interval of 3 percentage
points in either direction. Specifically,
the sample size is calculated assuming
that the universe is ‘‘infinite’’ and the
error rate for FFS is 5 percent and the
error rate for managed care is 3 percent.
(Once the universe contains more than
approximately 10,000 sampling units, it
can be treated as if it were infinite.
Statistically speaking, beyond a
universe of approximately 10,000
sampling units, universe size does not
affect sample size.) Using these
assumptions and historical information
on payment variation in FFS and
managed care from previous PERM
cycles, we have determined that an
annual sample of 500 FFS and 250
managed care payments per State per
program should meet our State-level
precision requirements with reasonable
probability.
However, States with Medicaid or
CHIP PERM universes under 10,000 line
items or capitation payments can
petition CMS for an annual sample size
smaller than the base sample size in the
initial PERM year or beyond. While the
universe can be treated as if it were
infinite if its size exceeds 10,000
sampling units, if the total universe
from which the total (full year) sample
is drawn is less than 10,000 sampling
units, the sample size may be reduced
by the finite population correction
factor. A State that anticipates that the
total number of payments in the FFS or
managed care universe for either
Medicaid or CHIP will be less than
10,000 payments over the Federal fiscal
year may notify CMS before the fiscal
year being measured and include
information on the anticipated universe
size for their State. Our contractor will
develop a modified sampling plan for
that program in that State.
The State-specific annual sample size
in the base PERM year is based on an
assumed error rate of 5 percent. If a
State’s actual PERM error rates in a
cycle reveals that precision goals can be
achieved in future PERM cycles with
either lower or higher sample sizes than
indicated by the original assumptions,
sample sizes after the first PERM cycle
may vary among States according to
each State’s demonstrated ability, based
on PERM experience, to meet desired
precision goals.
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In subsequent years, we will provide
our contractor with information on each
State’s error rate and payment variation
in the previous cycle. Our contractor
will review each State’s prior PERM
cycle claims error rate and payment
variation to determine if a smaller or
larger claims sample size will be
required to meet the precision goal
established for that PERM cycle. Our
contractor will develop a State-specific
sample size for each program in each
State. If information from a previous
cycle is not available for a particular
State or program within the State, the
contractor will use the ‘‘base sample’’
size of 500 FFS claims and 250 managed
care payments. For States measured in
the FY 2007 or FY 2008 cycle that elect
to accept their State-specific CHIP
PERM error rate determined during
those cycles, FY 2007 or FY 2008 would
be considered their first PERM cycle for
purposes of sample size calculation for
CHIP. Therefore, these States would be
considered for an adjusted sample size
in their next year of measurement after
the publication of the new final rule.
For States measured in the FY 2007 or
FY 2008 cycle that elect to reject their
State-specific CHIP PERM error rate
determined during those cycles,
information from those cycles would
not be used to calculate the Statespecific sample sizes and the ‘‘base
sample’’ size of 500 FFS claims and 250
managed care payments would be used.
We are proposing to establish a
maximum sample size for Medicaid or
CHIP FFS or managed care of 1,000
claims. Additionally, as discussed
above, a State with a claims universe of
less than 10,000 sampling units in a
program may notify CMS and the
annual sample size will be reduced by
the finite population correction factor
for any PERM cycle. We believe that by
taking into consideration prior cycle
PERM error rates, as well as the finite
population correction factor in
establishing State-specific sample sizes,
the States’ administrative cost burden
will be reduced and the program will be
manageable at the State level.
2. Eligibility
The eligibility sampling requirements
are described in § 431.978. The universe
for the eligibility component is casebased, not claims-based. The case as a
sampling unit only applies to the
eligibility component. For PERM
eligibility, the ‘‘universe’’ is the total
number of Medicaid or CHIP cases,
which, as discussed later in this
proposed rule, is comprised of all
beneficiaries, both individuals and
families. The eligibility sampling plan
and procedures state that the total
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eligibility sample size must be estimated
to achieve within a 3 percent precision
level at 95 percent confidence interval
for the eligibility component of the
program.
For PERM eligibility, the initial
sample size is calculated under the
assumption that the error rate is 5
percent and the universe is greater than
10,000 total cases. This means that the
desired precision requirements will be
achieved with a high probability if the
actual error rate is 5 percent or less. For
this reason, an annual sample of 504
active cases and 204 negative cases
should be selected in a State’s base
PERM year to meet State-level precision
requirements with a high probability.
Appendix D of the PERM Eligibility
Review Instructions elaborates on the
theory of sample size at the State-level
for the dollar-weighted active case error
rates, and is on the CMS Web site at
https://www.cms.hhs.gov/perm/
downloads/PERM_Eligibility_Review_
Guidance.pdf.
Eligibility sampling is performed by
the States, and States have the
opportunity to adjust their eligibility
sample size based on the eligibility error
rate in the previous PERM cycle. After
a State’s base PERM year, we will
determine, with input from the State, a
sample size that will meet desired
precision goals at lower or higher
sample sizes based on the outcome of
the State’s previous PERM cycle. The
sample size could either increase or
decrease given the results of the
previous year. We are proposing to
establish a maximum sample size for
eligibility at 1,000 cases. States must
submit an eligibility sampling plan by
August 1st before the fiscal year being
measured and include a proposed
sample size for their State. Our
contractor will review and approve all
eligibility sampling plans. The State
must notify CMS that it will be using
the same plan from the previous review
year if the plan is unchanged. However,
we will review State sampling plans
from prior cycles in each PERM cycle to
ensure that information is accurate and
up-to-date. States will be asked for
revisions when necessary.
As in the claims universe, States with
PERM eligibility universes under 10,000
cases can notify CMS for a reduced
eligibility sample size for either the base
year or any subsequent PERM cycle.
Additionally, section 203 of the
CHIPRA describes the State option to
enroll children in CHIP based on
findings of an express lane agency that
has conducted simplified eligibility
determinations. Under section
203(a)(13)(E) of the CHIPRA, an error
rate measurement will be created with
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respect to the enrollment of children
under the express lane eligibility option.
The law directs States not to include
children enrolled using the express lane
eligibility option starting April 1, 2009,
in data or samples used for purposes of
complying with MEQC and PERM
requirements. Provisions for States’
express lane option will be set forth in
a future rulemaking document.
We are proposing to revise § 431.814
and § 431.978 to reflect the changes and
clarifications specified above.
B. Error Criteria
Under the PERM program, we identify
improper payments through claims
reviews and eligibility reviews. For the
claims review, we perform the
following: (1) A data processing review
of a sample of FFS and managed care
payments to ensure the payments were
processed and paid in accordance with
State and Federal policy; and (2) a
medical review of a sample of FFS
payments to ensure that the services
were medically necessary, coded
correctly, and provided and
documented in accordance with State
and Federal policy. For the eligibility
review, we rely on States to review a
sample of beneficiary cases to ensure
that they were eligible for the program
and for any services received and paid
for by Medicaid or CHIP (as applicable).
The PERM eligibility review also
considers negative cases (cases where
eligibility was denied or terminated). A
negative case is in error if the case was
improperly denied or incorrectly
terminated. However, because there are
no payments associated with these
cases, only a case error rate is
calculated. These errors are not factored
into the PERM error rate, which is a
payment error rate.
Under the IPIA, to be considered an
improper payment, the error made must
affect payment under applicable Federal
policy and State policy. Improper
payments include both overpayments
and underpayments. A payment is also
considered improper where it cannot be
discerned whether the payment was
proper as a result of insufficient or lack
of documentation.
Consistent with the IPIA, the PERM
error rate itself does not distinguish
between ‘‘State’’ and ‘‘provider’’ errors;
all dollars in error identified through
PERM reviews contribute to the State
error rate. In practice, the data
processing and eligibility reviews focus
on determinations made by State
systems and personnel, while the
medical review focuses on
documentation maintained and claims
submitted by providers.
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Section 601(c)(1)(A) of the CHIPRA
requires CMS to promulgate a new final
rule that includes clearly defined
criteria for errors for both States and
providers. Accordingly, we are
proposing to add § 431.960, ‘‘Types of
payment errors,’’ to clarify that State or
provider errors for purposes of the
PERM error rate must affect payment
under applicable Federal policy and
State policy, and to generally categorize
data processing errors and eligibility
determination errors as State errors and
medical review errors as provider errors.
The data processing errors, medical
review errors, and eligibility
determination errors may include, but
are not limited to, the types of improper
payments discussed below.
1. Claims Review Error Criteria
a. Data Processing Errors (Generally
State Errors)
viii. Managed Care Rate Cell Error
The beneficiary was enrolled in
managed care and payment was made,
but for the wrong rate cell.
categories, including State-specific noncovered services.
ix. Managed Care Payment Error
The beneficiary was enrolled in
managed care and assigned to the
correct rate cell, but the amount paid for
that rate cell was incorrect.
i. Not Eligible
x. Other Data Processing Error
Errors not included in any of the
above categories.
b. Medical Review Errors (Generally
Provider Errors)
i. No Documentation
The provider did not respond to the
request for records within the required
timeframe.
ii. Insufficient Documentation
i. Duplicate Item
The sampled line item/claim is an
exact duplicate of another line item/
claim that was previously paid (for
example, same patient, same provider,
same date of service, same procedure
code, and same modifier).
ii. Non-Covered Service
The State policy indicates that the
service is not payable by Medicaid or
CHIP under the State plan and/or the
beneficiary is not in the coverage
category for that service.
There is not enough documentation to
support the service.
iii. Procedure Coding Error
The procedure was performed but
billed using an incorrect procedure code
and the result affected the payment
amount.
iv. Diagnosis Coding Error
According to the medical record, the
diagnosis was incorrect and resulted in
a payment error—as in a Diagnosis
Related Group (DRG) error.
iii. Fee-for-Service Claim for a Managed
Care Service
The beneficiary is enrolled in a
managed care organization that should
have covered the service, but the
sampled service was inappropriately
paid by the Medicaid or CHIP FFS
component.
iv. Third-Party Liability
The service should have been paid by
a third party and was inappropriately
paid by Medicaid or CHIP.
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v. Unbundling
The provider separately billed and
was paid for the separate components of
a procedure code when only one
inclusive procedure code should have
been billed and paid.
vi. Number of Unit(s) Error
The incorrect number of units was
billed for a particular procedure/service,
National Drug Code (NDC) units, or
revenue code.
c. Eligibility Errors (Generally State
Errors)
An individual beneficiary or family is
receiving benefits under the program
but does not meet the State’s categorical
and financial criteria in the first 30 days
of eligibility being verified.
ii. Eligible With Ineligible Services
An individual beneficiary or family
meets the State’s categorical and
financial criteria for receipt of benefits
under the Medicaid or CHIP program
but was not eligible to receive particular
services. An example of ‘‘eligible with
ineligible services’’ would be a person
eligible under the medically needy
group who received services not
provided to the medically needy group.
iii. Undetermined
A beneficiary case subject to a
Medicaid or CHIP eligibility
determination review under PERM and
which a definitive determination of
eligibility could not be made.
iv. Liability Overstated
The beneficiary paid too much toward
his liability amount or cost of
institutional care and the State paid too
little.
v. Liability Understated
Beneficiary paid too little toward his
liability amount or cost of institutional
care and the State paid too much.
vi. Managed Care Error 1
Ineligible for managed care—Upon
verification of residency and program
eligibility, the beneficiary is enrolled in
managed care but is not eligible for
managed care.
vii. Managed Care Error 2
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v. Pricing Error
Payment for the service does not
correspond with the pricing schedule on
file for the date of service.
The service was medically
unnecessary based upon the
documentation of the patient’s
condition in the medical record.
Eligible for managed care but
improperly enrolled—Beneficiary is
eligible for both the program and for
managed care but not enrolled in the
correct managed care plan as of the
month eligibility is being verified.
vi. Logic Edit
A system edit was not in place based
on policy or a system edit was in place
but was not working correctly and the
claim line was paid (for example,
incompatibility between gender and
procedure).
viii. Policy Violation
viii. Improper Denial
A policy is in place regarding the
service or procedure performed and
medical review indicates that the
service or procedure is not in agreement
with the documented policy.
The application for program benefits
was denied by the State for not meeting
the categorical and/or financial
eligibility requirements but upon review
is found to be eligible.
ix. Administrative/Other Medical
Review Error
ix. Improper Termination
vii. Data Entry Errors
A claim/line item is in error due to
clerical errors in the data entry of the
claim.
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vii. Medically Unnecessary Service
A payment error was determined by
the medical review but does not fit into
one of the other medical review error
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Based on a completed
redetermination, the State determines
an existing beneficiary no longer meets
the program’s categorical and/or
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financial eligibility requirements and is
terminated but upon review is found to
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2. Definitions
Based on the criteria identified in
section II.B.1 of this proposed rule, we
are proposing to add the following
definitions for ‘‘provider error’’ and
‘‘State error’’ to § 431.958.
Provider error includes, but is not
limited to, an improper payment made
due to lack of or insufficient
documentation, incorrect coding,
improper billing (for example,
unbundling, incorrect number of units),
a payment that is in error due to lack of
medical necessity, or evidence that the
service was not provided in compliance
with documented State or Federal
policy.
State error includes, but is not limited
to the following:
• A payment that is in error due to
incorrect processing (for example,
duplicate of an earlier payment,
payment for a non-covered service,
payment for an ineligible beneficiary).
• Incorrect payment amount (for
example, incorrect fee schedule or
capitation rate applied, incorrect thirdparty liability applied).
• A payment error resulting from
services being provided to an individual
who—
++ Was ineligible when authorized
or when he or she received services;
++ Was eligible for the program but
was ineligible for certain services he or
she received; or
++ Had not met applicable
beneficiary liability requirements when
authorized eligible or paid too much
toward actual liability.
++ Had a lack of sufficient
documentation to make a definitive
determination of eligibility or
ineligibility.
C. Self-Declaration of Eligibility
Section 601(c)(2) of the CHIPRA
requires that the payment error rate
determined for a State shall not take
into account payment errors resulting
from the State’s verification of an
applicant’s self-declaration or selfcertification of eligibility for, and the
correct amount of, medical assistance or
child health assistance, if the State
process for verifying an applicant’s selfdeclaration or self-certification satisfies
the requirements for such process
applicable under regulations
promulgated by the Secretary or
otherwise approved by the Secretary.
Accordingly, we are proposing to
specify in the new § 431.960 that the
dollars paid in error due to the
eligibility error is the measure of the
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payment error. A State eligibility error
does not result from the State’s
verification of an applicant’s selfdeclaration or self-certification of
eligibility for, and the correct amount of,
medical assistance or child health
assistance, if the State process for
verifying an applicant’s self-declaration
or self-certification satisfies the
requirements for such process
applicable under regulations at
§ 457.380 of this chapter, in CMS
approved State Plans, or otherwise
approved by the Secretary.
We also propose to modify § 431.980
to provide review requirements for
acceptable self-declaration. We would
also modify the PERM eligibility
instructions, found at https://
www.cms.hhs.gov/perm/downloads/
PERM_Eligibility_Review_Guidance.pdf.
These instructions, which clarify and
provide additional guidance in
implementing the regulations, reflect
the new review procedures for self
declaration.
Currently, States are required to
review the case record and
independently verify elements of
eligibility where evidence is missing, or
outdated and likely to change, or
otherwise as needed. The instructions
and the regulation would provide that
‘‘a self-declaration statement for
Medicaid or CHIP is acceptable
verification for the PERM reviews for
elements of eligibility in which State
policy allows for self-declaration. A selfdeclaration statement must be—
• Present in the record;
• Not outdated (more than 12 months
old);
• In a valid, State approved format;
and
• Consistent with other facts in the
case record.
A State may verify eligibility through
a new self-declaration statement,
depending on State policies on selfdeclaration. We propose that if a new
self-declaration statement cannot be
obtained for the PERM review, the State
may verify eligibility using third party
sources, for example, documentation
listed in section 7269 of the State
Medicaid Manual. Verifying a selfdeclaration statement with third party
verification when a beneficiary does not
provide a new self-declaration statement
is the only new review procedure being
added. After all minimum efforts listed
in the eligibility instructions have been
exhausted, a case should be cited as
Undetermined if sufficient
documentation cannot be obtained to
complete the eligibility review. We are
proposing that these Undetermined
cases would not be included in the
State-specific payment error rate.
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However, we are proposing to specify in
the new § 431.960 that these errors be
tracked nationally by including these
Undetermined cases in the national
program payment error rates.
D. Difference Resolution and Appeals
Process
Section 601(c)(1)(B) of the CHIPRA
requires CMS to include in the new
final rule for PERM a clearly defined
process for appealing error
determinations by review contractors or
State agency and personnel responsible
for the development, direction,
implementation, and evaluation of
eligibility reviews and associated
activities.
1. Medical and Data Processing Review
The October 5, 2005 IFC established
the difference resolution process, which
is codified at § 431.998. Medical reviews
and data processing reviews for FFS and
managed care payments are conducted
by an independent Federal contractor.
States supply relevant policies but do
not participate in the review; States are
notified of all error findings. The
difference resolution process is the
mechanism by which a State may try to
resolve with the Federal contractor
differences in the Federal contractor’s
error findings; the State may appeal to
CMS if it cannot resolve the difference
in findings with the Federal contractor.
In accordance with the CHIPRA, we
are providing more detail in this
proposed rule by proposing the timeline
associated with the difference resolution
and CMS appeals processes. We are also
revising the heading of § 431.998 to
read, ‘‘Difference resolution and appeal
process,’’ which more accurately
describes the regulation.
We are proposing to revise § 431.998
to explain that the State may file, in
writing, a request with the Federal
contractor to resolve differences in the
Federal contractor’s findings based on
medical or data processing reviews of
FFS and managed care claims in
Medicaid or CHIP within 10 business
days after the disposition report of
claims review findings is posted on the
contractor’s Web site. Additionally, the
State may appeal to CMS for a final
resolution within 5 business days from
the date the contractor’s finding as a
result of the difference resolution is
posted on its Web site.
In addition to establishing the
timeline for the difference resolution
and appeal processes, we are proposing
to eliminate the dollar threshold for
engaging in the CMS appeals process.
Section 431.998 currently provides that
States may apply to the Federal
contractor to resolve differences in
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findings and may appeal to CMS for
final resolution for any claims in which
the State and Federal contractor cannot
resolve the difference in findings, as
long as the difference in findings is in
the amount of $100 or more. We
established the $100 threshold in order
to prevent de minimis disputes and to
ensure that appeals to CMS were
substantial enough to warrant
reconsideration. We were also
concerned that a large volume of smalldollar appeals would prevent the States
from receiving timely decisions on their
appeals.
Information from the FY 2006 and FY
2007 PERM cycles on the number of
total claims (including those with errors
less than $100) submitted to the Federal
contractor for difference resolution and
on the number appealed to CMS for
final resolution suggests that the volume
of appeals will not substantially
increase if CMS allows appeals of errors
of less than $100. Because all errors
regardless of their dollar amount
ultimately contribute to a State’s error
rate and hence the national error rate,
we are proposing to remove the $100
threshold set forth in § 431.998(b)(1).
2. Eligibility
As stated in the current PERM
regulations at § 431.974(a)(2), personnel
responsible for PERM eligibility
sampling and review ‘‘must be
functionally and physically separate
from the State agencies and personnel
that are responsible for Medicaid and
CHIP policy and operations, including
eligibility determinations.’’ The intent
of this provision was to ensure the
independence of the review in order to
achieve an unbiased error rate. We
provided further clarification in the
preamble of the August 2007 final rule,
indicating that the agency responsible
for PERM could be under the same
umbrella agency that oversees policy,
operations and determinations but the
two agencies cannot report to the same
supervisor.
We would further clarify that
qualified staff with knowledge of State
eligibility policies may be used to
conduct the eligibility reviews, but the
staff that is chosen must be independent
from the staff that oversees policy and
operations. Further, the PERM eligibility
instructions ask States to provide
assurance that the agency or contracting
entity responsible for the eligibility
reviews is independent of the State
agency responsible for eligibility
determination and enrollment. The
State is responsible for ensuring the
integrity of the eligibility reviews, but
we do not preclude the independent
State agency from sharing or reporting
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the eligibility findings to other agencies
or stakeholders.
Provided that agency independence
could cause a difference in findings
between the independent agency and
other stakeholder agencies at the State
level, we propose that appeals for
eligibility review findings should be
conducted in accordance with the
State’s appeal process, as eligibility
reviews are conducted at the State level.
In consideration of States that may
not have a State appeals process in
place, we are also proposing to make
State findings available to each
respective State’s stakeholders (that is,
the State Medicaid or CHIP agency),
with certain limitations, for the period
between the final monthly payment
findings submission and eligibility error
rate calculation, for example, April 15th
through June 15th after the fiscal year
being measured or according to the
eligibility timeline. We propose
facilitating documentation exchange
between the State Medicaid or CHIP
agency and the independent State
agency conducting the PERM eligibility
reviews to resolve differences. If any
eligibility appeals issues involve
Federal policy, States can appeal to
CMS for resolution. If our decision
causes an erroneous payment finding to
be made, any resulting recoveries will
be governed by § 431.1002.
Other stakeholder agencies may
document their differences in writing to
the independent State agency for
consideration. If resolutions of
differences occur during the PERM
cycle, eligibility findings can be
updated to reflect the resolution. If
differences are not resolved by the
deadline for eligibility findings to be
submitted to CMS (July 1), the
documentation of the difference can be
submitted to CMS for consideration no
sooner than 60 days and no later than
90 days after the deadline for eligibility
findings.
We are also seeking comment on other
ways that we can implement an
eligibility appeals process for which we
can provide consistent oversight.
E. Harmonization of Medicaid Eligibility
Quality Control (MEQC) and PERM
Programs
1. Options for Applying PERM and
MEQC Data
Section 601(e)(2) of the CHIPRA
requires that, once this final rule is
effective for all States, States will be
given the option to elect, for purposes
of determining the erroneous excess
payments for medical assistance ratio
applicable to the State for a fiscal year
under section 1903(u) of the Act, to
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substitute data resulting from the
application of the PERM requirements
to the State for data obtained from the
application of the MEQC requirements
to the State with respect to a fiscal year.
Because under section 601(b) of the
CHIPRA, there shall be no calculation or
publication of any national or Statespecific CHIP error rates until 6 months
after the final rule becomes effective,
States will not have the option to
substitute PERM data for MEQC data
until 6 months after this final rule is
effective.
We considered several interpretations
of the CHIPRA requirements that would
allow States the option to substitute
MEQC data for PERM data and vice
versa for purposes of the PERM
Medicaid eligibility reviews, but would
also retain two separate, independent
processes (MEQC and PERM), which are
governed by separate statutes and
regulations. As PERM is required to
meet specific statistical precision
requirements and the MEQC error rate is
not, we do not believe it is feasible to
incorporate the MEQC error rate into a
State’s overall PERM error rate.
Therefore, we interpret ‘‘data’’ as the
sample, eligibility review findings, and
payment findings as measured under
MEQC or PERM. We will calculate
separate rates for each program. We are
proposing to amend § 431.806 and
§ 431.812 of the MEQC regulations.
These proposed amendments would
provide for the State’s option in its
PERM year to use their samples,
eligibility findings and payment
findings as measured using PERM
sampling and review requirements to
meet their MEQC review requirement.
States operating under MEQC waivers
and pilot programs cannot use this
option. Therefore, to provide
requirements for implementing a pilot
or waiver MEQC program, we are
proposing revisions to the MEQC
regulation at § 431.812. We are
proposing that States that choose to
substitute PERM data for MEQC data,
would still have two eligibility error
rates calculated –- one for MEQC using
MEQC measurement requirements and
one for PERM using PERM
requirements. We are proposing to
revise § 431.806 of the MEQC
regulations to require that a State plan
provide a State plan amendment for
States opting to use PERM for MEQC in
a State’s PERM cycle.
We are proposing to amend § 431.812
of the MEQC regulation to provide that
States substituting PERM data for MEQC
data must use a sampling plan that
meets the requirements of § 431.978 of
the PERM regulation and perform active
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case reviews in accordance with
§ 431.980 of the PERM regulation.
We are proposing that States with
CHIP stand alone programs will only
have the option to substitute PERM
Medicaid data to meet MEQC
requirements under § 431.812(a)
through (e) since CHIP stand alone
programs are not reviewed under
MEQC.
We are also proposing that States with
Medicaid and Title XXI Medicaid
expansion programs may use Medicaid
and CHIP PERM reviews to meet the
MEQC requirements described under
§ 431.812(a) through (e), as both
Medicaid and Title XXI Medicaid
expansion programs are reviewed under
MEQC. States with Title XXI Medicaid
expansion programs must combine their
Medicaid and CHIP PERM findings to
calculate one MEQC error rate. The data
must be kept separate for purposes of
calculating the PERM error rate.
In addition, we are proposing that
States with combination CHIP programs,
in which a portion of their CHIP cases
are under a stand alone program and a
portion of their CHIP cases are under a
Title XXI Medicaid expansion program,
may use the PERM Medicaid eligibility
reviews and the portion of the PERM
CHIP eligibility reviews under Title XXI
Medicaid expansion programs to meet
their MEQC requirement. The Federal
contractor will combine the CHIP case
findings under the Title XXI Medicaid
expansion program and CHIP stand
alone findings to calculate one PERM
CHIP error rate. The Title XXI Medicaid
expansion portion of the PERM data
must be included with the Medicaid
PERM data to calculate the MEQC error
rate.
Section 601(e)(3) of the CHIPRA
provides that for purposes of satisfying
the requirements of the PERM
regulation relating to Medicaid
eligibility reviews, a State may elect to
substitute data obtained through MEQC
reviews conducted in accordance with
section 1903(u) of the Act for data
required for purposes of PERM
requirements, but only if the State
MEQC reviews are based on a broad,
representative sample of Medicaid
applicants or enrollees in the States.
The CHIPRA’s general effective date of
April 1, 2009 applies to this provision.
Therefore, as of April 1, 2009, States
have the option to substitute MEQC data
for PERM data so long as the MEQC
reviews are based on a broad,
representative sample of Medicaid
applicants or enrollees in the States.
We interpret ‘‘broad, representative
sample of Medicaid applicants or
enrollees’’ to mean that States must
develop the MEQC universe according
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to requirements at § 431.814 in order to
consider the option to use one
program’s findings to meet the
requirements for the other. Under
§ 431.814, States must sample from a
universe of all Medicaid and Title XXI
Medicaid expansion beneficiaries
(except for the exclusions provided in
§ 431.814(c)(4)). States operating MEQC
pilots or waivers will need to continue
operating PERM separately from MEQC.
We are proposing that States with
CHIP stand alone programs only have
the option to substitute Medicaid MEQC
data to meet the PERM Medicaid
eligibility review requirement, as CHIP
stand alone is not reviewed under the
MEQC review.
We are also proposing that States with
Title XXI Medicaid expansion programs
may use their MEQC reviews described
in § 431.812(a) through (e) to meet both
the PERM Medicaid and CHIP eligibility
review requirements, as both Medicaid
and Title XXI Medicaid expansion are
reviewed under MEQC. Title XXI
Medicaid expansion data must be
separated from the MEQC Medicaid data
to calculate a PERM CHIP error rate.
We are also proposing that States with
combination programs in which a
portion of their CHIP cases are under a
stand alone program and a portion of
their CHIP cases are under a Title XXI
Medicaid expansion program may use
the MEQC reviews described under
§ 431.812 (a) through (e) to meet the
PERM Medicaid eligibility review
requirement and the portion of the
PERM CHIP eligibility review
requirement under Title XXI Medicaid
expansion. However, the stand alone
portion of the CHIP universe must
remain separate and stratified, as
defined in § 431.978(d)(3), as CHIP
stand alone is not a part of the
harmonization of PERM and MEQC. The
Federal contractor, who we are
proposing will calculate State eligibility
error rates, will combine the Title XXI
Medicaid expansion and CHIP stand
alone findings to calculate one PERM
CHIP error rate.
In addition, we are proposing to
amend § 431.980 to allow for States in
their PERM year the option to use their
MEQC samples, eligibility findings, and
payment findings to meet their PERM
eligibility review requirement. MEQC
reporting requirements to the CMS
Regional Offices remain the same,
including reporting the error findings
for the two 6-month review periods, but
States will also be required to comply
with the PERM eligibility reporting
deadlines by posting error findings to
the PERM Error Rate Tracking (PERT)
Web site or other electronic eligibility
findings repository specified by CMS.
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We are proposing that States that choose
to substitute MEQC data for PERM data,
will still have two eligibility error rates
calculated—one for MEQC using MEQC
measurement requirements and one for
PERM using PERM requirements.
States that choose to substitute MEQC
data must ensure that the Medicaid and
Title XXI Medicaid expansion sample
sizes meet PERM precision
requirements when they are separated.
States must also note that if using
MEQC data, any cases sampled under
§ 431.814(c)(4) must be excluded from
the PERM sample. For example, Stateonly funded cases, should be reported
separately.
States that choose to substitute MEQC
or PERM data should note that although
two error rates are calculated, only the
MEQC error rate will be subject to
disallowances under section 1903(u) of
the Act. PERM does not have a
threshold for eligibility errors and any
improper payments identified during
the eligibility measurement are subject
to recovery according to § 431.1002 of
the regulations.
If a State chooses to substitute PERM
or MEQC data, the State may not
dispute error findings or the eligibility
error rate based on the possibility that
findings would not have been in error
had the other review methodology been
used.
We are also seeking comments on the
following alternative process for the
substitution of MEQC and PERM data:
States would select one annual sample
that meets MEQC minimum sample
requirements and PERM confidence and
precision requirements. The State
would conduct both an MEQC review
and a PERM review on each applicable
case. This would ensure a clear
distinction between an MEQC error and
a PERM eligibility error, and will be the
basis for the MEQC error rate and the
PERM eligibility error rate. We are also
seeking comment on other possible
methods for substitution of data.
States that choose to substitute MEQC
data may only claim the regular
administrative matching rate for
performing the MEQC procedures for
Medicaid and Title XXI Medicaid
expansion cases. The 90 percent PERM
enhanced administrative matching rate
will only be applicable to States
conducting PERM reviews for CHIP
cases.
2. Definition of a Case
Section 431.958 currently defines a
case as an ‘‘individual beneficiary.’’
States are required to sample and
conduct eligibility and payment reviews
for an individual beneficiary even if the
State grants eligibility at the family
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level. However, sampling at the
individual beneficiary level has proven
to be difficult for States from a
programming perspective.
Many States receive, review, and
grant eligibility based on an application
for an entire family, which could be for
one person or multiple people. Dividing
the family unit for PERM eligibility
sampling has been difficult for States to
achieve. In addition, the CHIPRA
requires MEQC and PERM
harmonization to reduce the burden on
States.
The MEQC regulation, at § 431.804,
defines an active case, in pertinent part,
as an ‘‘individual [beneficiary] or
family.’’ Changing the definition of a
case for PERM eligibility to include both
individual beneficiaries and families
will support the harmonization process
by making it easier for States to utilize
their new option of substituting PERM
data for MEQC data, and vice versa.
Therefore, we are proposing to revise
the definition of a case in § 431.958 to
mean an individual or family.
3. Error Rate Calculation: State
Responsibility for Calculating Error
Rates
Section 431.988 requires, as part of
the PERM eligibility review process, for
States to calculate and report case and
payment error rates for active cases and
case error rates for negative cases. As
originally envisioned, States retained
responsibility for sampling cases,
conducting eligibility reviews,
collecting payment information for
errors, and calculating eligibility error
rates. States were to report final
eligibility error rates to CMS, which will
forward the information to the Federal
contractor for inclusion in the overall
State and national error rates.
In practice, States have found it
difficult to calculate the eligibility error
rates. In most cases, States lack the
necessary statistical or technical
expertise to execute the error rate
calculation formulas provided in the
PERM eligibility instructions. During
the FY 2007 cycle, the Federal
contractor provided substantial
technical assistance to the States to
assist them in conducting these
calculations including developing a
spreadsheet that States could use to
perform the required calculations.
Several States requested that, rather
than have the Federal contractor
provide a spreadsheet that the States
merely populate and return to CMS, the
Federal contractor perform the required
calculations.
Initially, we did not consider it
feasible for the Federal contractor to
conduct the PERM eligibility error rate
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calculations because the States conduct
the reviews and maintain the case and
payment error data. However, during FY
2007, we developed a centralized
reporting system for monthly case and
payment error data. The Federal
contractor can access the centralized
system to conduct the eligibility error
rate calculations.
Given the difficulties States have
experienced in calculating the PERM
eligibility error rates and that there are
now mechanisms and processes for the
Federal contractor to calculate these
error rates, we are proposing to revise
§ 431.988(b)(1) and (b)(2) by replacing
‘‘rates’’ with ‘‘data’’ to read as follows:
‘‘The agency must report by July 1
following the review year, information
as follows: (1) Case and payment error
data for active cases; and (2) Case error
data for negative cases.’’
We maintain that this approach will
reduce the burden on the States and
more accurately reflect current practice,
which is that the Federal contractor
calculates the eligibility error rates used
in the generation of the PERM error rate,
as well as the State and national-level
error rates. We will continue to require
States to report data to the centralized
reporting system and will provide States
with a spreadsheet or similar calculator
that can be used to estimate their own
eligibility error rates, but will not
require States to submit these estimates
to CMS.
F. Corrective Action Plans
Section 601(c)(1)(C) of the CHIPRA
requires CMS to provide defined
responsibilities and deadlines for States
in implementing corrective action plans.
1. Corrective Action Plan Due Dates
We are proposing to revise § 431.992
to provide that States would be required
to submit to CMS and implement the
corrective action plan for the fiscal year
it was reviewed no later than 60
calendar days from the date the State’s
error rate is posted to the CMS
Contractor’s Web site. State error rates
will be posted to the Web site no later
than November 15 of each calendar
year.
2. Types of Plans
In addition to measuring programs at
risk for significant improper payments,
the IPIA also requires a report on
Federal agency actions taken to reduce
improper payments. Since States
administer Medicaid and CHIP and
make payments for services rendered
under these programs, it is necessary
that States take corrective actions to
reduce improper payments at the State
level. We issued a State Health Official
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34477
letter in October 2007 to all States
detailing the corrective action process
under PERM, which can be found on the
CMS PERM Web site at https://
www.cms.hhs.gov/PERM/Downloads/
Corrective_Action_Plan.pdf.
The corrective action process is the
means by which States take
administrative actions to reduce errors
which cause misspent Medicaid and
CHIP dollars. The corrective action
process involves analyzing findings
from the PERM measurement,
identifying root causes of errors and
developing corrective actions designed
to reduce major error causes, and trends
in errors or other factors for purposes of
reducing improper payments.
Development, implementation, and
monitoring of the corrective action plan
are the responsibility of the States. In
order to develop an effective corrective
action plan, States must perform data
and program analysis, as well as plan,
implement, monitor, and evaluate
corrective actions. We are proposing to
revise § 431.992 to define States’
responsibilities for these activities as
explained below.
(1) Data Analysis—States must
conduct data analysis such as reviewing
clusters of errors, general error causes,
characteristics, and frequency of errors.
States must also consider improper
payments associated with errors. Data
analysis may sort the predominant
payment errors and number of errors as
follows:
• Type—general classification (for
example, FFS, managed care,
eligibility).
• Element—specific type of
classification (for example, no
documentation errors, duplicate claims,
ineligible cases due to excess income).
• Nature—cause of error (for example,
providers not submitting medical
records, lack of systems edits,
unreported changes in income that
caused ineligibility). For the eligibility
component, States must analyze both
active and negative case errors and also
causes for undetermined case findings.
(2) Program Analysis—States must
review the findings of the data analysis
to determine the specific programmatic
causes to which errors are attributed (for
example, a provider’s lack of
understanding of section 1902(a)(27) of
the Act and § 457.950 of the regulations
requiring providers to submit
information regarding payments and
claims as requested by the Secretary,
State agency, or both) and to identify
root error causes. The States may need
to analyze the agency’s operational
policies and procedures and identify
those policies or procedures that
contribute to errors, for example,
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policies that are unclear, or there is a
lack of operational oversight at the local
level.
(3) Corrective Action Planning—States
must determine the corrective actions to
be implemented that address the root
error causes.
(4) Implementation and Monitoring—
States must implement the corrective
actions in accordance with an
implementation schedule. States must
develop an implementation schedule for
each corrective action initiative and
implement those actions. The
implementation schedule must identify
major tasks, key personnel responsible
for each activity, and must include a
timeline for each action including target
implementation dates, milestones, and
monitoring.
(5) Evaluation—States must evaluate
the effectiveness of the corrective action
by assessing improvements in
operations, efficiencies, and the
incidence of payment errors or number
of errors. Subsequent corrective action
plans that are submitted as a result of
the State’s next measurement must
include updates on the following
previous actions: (1) Effectiveness of
implemented corrective actions using
concrete data; (2) discontinued or
ineffective actions, and actions not
implemented and what actions were
used as replacements; (3) findings on
short-term corrective actions; and (4) the
status of the long-term corrective
actions.
In addition, we are proposing that
CMS would review and approve the
corrective action plans submitted by
States, and may request regular updates
on the approved corrective actions. We
are soliciting public comments on the
timeline and process associated with
this review and approval.
III. Additional Issues Soliciting Public
Comments
We are exploring options for the
future management of the CHIP and
Medicaid PERM programs. We welcome
input on components of the program.
When submitting input, please address
the following details:
• Data source;
• Sampling methodology;
• Medical and data processing
reviews;
• Reporting;
• Appeals.
We are soliciting public comments
and may consider them in a future
rulemaking effort.
IV. Collection of Information
Requirements
Under the Paperwork Reduction Act
of 1995, we are required to provide 60-
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day notice in the Federal Register and
solicit public comment before a
collection of information requirement is
submitted to the Office of Management
and Budget (OMB) for review and
approval. In order to fairly evaluate
whether an information collection
should be approved by OMB, section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires that we
solicit comment on the following issues:
• The need for the information
collection and its usefulness in carrying
out the proper functions of our agency.
• The accuracy of our estimate of the
information collection burden.
• The quality, utility, and clarity of
the information to be collected.
• Recommendations to minimize the
information collection burden on the
affected public, including automated
collection techniques.
We are soliciting public comment on
each of these issues for the following
sections of this document that contain
information collection requirements
(ICRs):
A. ICRs Regarding Review Procedure
(§ 431.812)
Section 431.812(a)(1) states that
except as provided in paragraph (a)(2) of
this section, the agency must review all
active cases selected from the State
agency’s lists of cases authorized
eligible for the review month, to
determine if the cases were eligible for
services during all or part of the month
under review, and, if appropriate,
whether the proper amount of recipient
liability was computed. In § 431.812,
proposed paragraph (g) states that a
State in its PERM year may elect to
substitute the random sample of
selected cases, eligibility review
findings, and payment review findings
obtained through PERM reviews
conducted in accordance with § 431.980
of the regulations for data required in
this section, where the only exclusions
are those set forth in § 431.978(d)(1) of
this regulation. The burden associated
with this requirement is the time and
effort necessary to complete the review
of active cases. The burden associated
with this requirement is currently
approved under OMB control number
0938–0147 with an October 31, 2009,
expiration date.
States in their PERM year that elect to
substitute PERM data to meet the
requirements of § 431.812 would
significantly reduce the burden
associated with reviewing active cases
for MEQC. The burden associated with
the information collection requirements
contained in proposed § 431.812(g) is
the time and effort necessary for a State
to substitute the random sample of
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selected cases, eligibility review
findings, and payment review findings
obtained through PERM reviews
conducted in accordance with
§ 431.980. Currently, we believe 19
States (12 Medicaid States and 7 CHIP
States) can elect the data substitution
and comply with this requirement. We
estimate that it would take each agency
10,055 hours to comply with the
information collection requirements. In
subsequent years, we expect that more
States will elect to substitute data from
section § 431.980 to meet this
requirement so we are estimating the
maximum burden for 34 States (17
Medicaid States and 17 CHIP States).
The total burden associated with the
requirements in proposed § 431.812(g) is
341,870 hours.
Although the review burden would be
significantly reduced, States would still
be required to report PERM and MEQC
findings separately. The additional
burden is explained in the section
below for § 431.980. We will submit a
revised information collection request
for 0938–0147 to account for the
increased burden as a result of the
requirements proposed in § 431.812(g).
B. ICRs Regarding MEQC Sampling Plan
and Procedures (§ 431.814)
Section 431.814 states that an agency
must submit a basic MEQC sampling
plan (or revisions to a current plan) that
meets the requirements of this section to
the appropriate CMS Regional Office for
approval at least 60 days before the
beginning of the review period in which
it is to be implemented. The burden
associated with this requirement is the
time and effort necessary to draft and
submit a new sampling plan or to draft
and submit a revised sampling plan to
the appropriate CMS Regional Office.
While this requirement is subject to the
PRA, it is currently approved under
OMB control number 0938–0146 with
an October 31, 2009, expiration date.
C. ICRs Regarding PERM Eligibility
Sampling Plan and Procedures
(§ 431.978)
In § 431.978, the proposed revisions
to paragraph (a) discuss the
requirements for sampling plan
approval. Specifically, the proposed
revision to § 431.978(a)(1) states that for
each review year, the agency must
submit a State-specific Medicaid or
CHIP sampling plan (or revisions to a
current plan) for both active and
negative cases to CMS for approval by
the August 1 before the review year and
must receive approval of the plan before
implementation. The proposed revision
to § 431.978(a)(2) further explains that
the agency must notify CMS that it
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would be using the same plan from the
previous review year if the plan is
unchanged.
The burden associated with the
information collection requirements
contained in § 431.978(a) is the time and
effort necessary for State agencies to
draft and submit the aforementioned
information to CMS. While this
requirement is subject to the PRA, the
associated burden is approved under
OMB control number 0938–1012 with a
January 31, 2010, expiration date.
D. ICRs Regarding Eligibility Review
Procedures (§ 431.980)
Proposed § 431.980(d) states that
unless the State has elected to substitute
MEQC data for PERM data under
paragraph (f) of this section, the agency
must complete the following.
Specifically, proposed § 431.980(d)(iii)
requires a State to examine the evidence
in the case file that supports categorical
and financial eligibility for the category
of coverage in which the case is
assigned, and independently verify
information that is missing, older than
12 months and likely to change, or
otherwise as needed, to verify
eligibility. Section 431.980(d)(vi) states
that the elements of eligibility in which
State policy allows for self declaration
can be verified with a new selfdeclaration statement. Proposed
§ 431.980(vii) contains the requirements
for a self-declaration statement.
The burden associated with the
requirements contained in proposed
§ 431.980 is the time and effort
necessary for a State agency to complete
the aforementioned requirements. While
this requirement is subject to the PRA,
the associated burden is currently
approved under OMB control number
0938–1012.
Proposed § 431.980(f)(1) allows for a
State in its PERM year to elect to
substitute the random sample of
selected cases, eligibility review
findings, and payment reviews findings
obtained through MEQC reviews
conducted in accordance with section
1903(u) of the Act to meet its PERM
eligibility review requirement. The
substitution of the MEQC data is
allowed as long as the State MEQC
reviews are based on a broad,
representative sample of Medicaid
applicants or enrollees in the State. In
addition, as stated in proposed
§ 431.980(f)(2), the MEQC samples must
also meet PERM confidence and
precision requirements.
The burden associated with the
information collection requirements
contained in proposed § 431.980(f) is
the time and effort necessary for a State
to collect, review, and submit the MEQC
data as part of meeting its PERM
eligibility review requirement. States
that elect to substitute MEQC data to
complete the requirements of § 431.980
would significantly reduce the burden
associated with reviewing active cases
for PERM. Although the review burden
would be eliminated, States would still
be required to report PERM and MEQC
findings separately. Currently we
believe 19 States (12 Medicaid States
and 7 CHIP States) can elect the data
substitution and comply with this
requirement. We estimate that it would
take each agency 10,500 hours to
comply with the information collection
requirements. In subsequent years, we
expect that more States will elect to
substitute data from section § 431.812 to
meet this requirement so we are
estimating the maximum burden for 34
States (17 Medicaid States and 17 CHIP
States). The total burden associated with
the requirements in proposed
§ 431.980(f) is 357,000 hours.
We also propose adding additional
burden as stated above. States must
report PERM and MEQC findings
separately and will use an estimated 2
34479
hours per required form to reformat
PERM or MEQC data into the
appropriate forms. We are adding an
additional 98 hours for each State to
reformat MEQC data into the
appropriate PERM eligibility forms and
98 hours for each State to compile
PERM eligibility data to submit on the
appropriate MEQC forms. We will
submit a revised information collection
request for 0938–1012 to account for the
increased burden as a result of the
requirements proposed in § 431.980(f).
E. ICRs Regarding Corrective Action
Plan (§ 431.992)
The proposed revisions to
§ 431.992(a) specify that State agencies
must submit to CMS a corrective action
plan to reduce improper payments in its
Medicaid and CHIP programs based on
its analysis of the error causes in the
FFS, managed care, and eligibility
components. In § 431.992(b), we are
proposing to revise this section to
require States to submit a corrective
action plan to CMS for the fiscal year it
was reviewed no later than 60 days from
the date the State’s error rate is posted
to the CMS Contractor’s Web site. As
proposed in § 431.992(c), States will be
required to implement corrective
actions in accordance with their
corrective action plans as submitted to
CMS. Proposed § 431.992(d) details the
required components of a corrective
action plan.
The burden associated with the
information collection requirements in
proposed revisions to § 431.992 is the
time and effort necessary for States to
develop corrective action plans, submit
the plans to CMS, and implement
corrective actions as dictated by their
corrective plans. While these
requirements are subject to the PRA, the
burden is approved under the OMB
control numbers shown in Table 1.
TABLE 1—OMB CONTROL NUMBERS
OMB control
No.
Expiration
date
Fee-for-Service .............................................................................................................................................................
Managed Care ..............................................................................................................................................................
Eligibility ........................................................................................................................................................................
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Program component
0938–0974 ..
0938–0994 ..
0938–1012 ..
02/29/2012
09/30/2009
01/31/2010
F. ICRs Regarding Difference Resolution
and Appeal Process (§ 431.998)
As proposed in § 431.998(a), a State
may file, in writing, a request with the
Federal contractor to resolve differences
in the Federal contractor’s findings
based on medical or data processing
reviews on FFS and managed care
claims in Medicaid and CHIP within 10
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business days after the disposition
report of claims review findings is
posted on the contractor’s Web site. The
written request must include a factual
basis for filing the difference and it must
provide the Federal contractor with
valid evidence directly related to the
error finding to support the State’s
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position that the claim was properly
paid.
Proposed § 431.998(b) states that for a
claim in which the State and the Federal
contractor cannot resolve the difference
in findings, the State may appeal to
CMS for final resolution within 5
business days from the date the
contractor’s finding as a result of the
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difference resolution is posted on its
Web site.
Proposed § 431.998(c) states that for
eligibility error determinations made by
agencies or personnel functionally and
physically separate from the State
agencies and personnel that are
responsible for Medicaid and CHIP
policy and operations, the State may
appeal error determinations by filing a
request with the appropriate State
agencies. If no appeals process is in
place at the State level, differences in
findings must be documented in writing
for the independent State agency to
consider. Any unresolved differences
may be addressed by CMS between the
final month of payment data submission
and error rate calculation. CMS may
facilitate documentation exchange to
assist in resolving difference at the State
level. Any changes in error findings
must be reported to CMS by the
deadline for submitting final eligibility
review findings. Any appeals of
determinations based on interpretations
of Federal policy may be referred to
CMS.
The burden associated with the
information collection requirements
contained in proposed § 431.998(a)
through (c) is the time and effort
necessary to draft and submit requests
for difference resolution proceedings
and determination appeals. We believe
the burden associated with these
requirements are exempt from the PRA
under 5 CFR 1320.4. Information
collected subsequent to an
administrative action is not subject to
the PRA.
G. OMB Control Number(s) for
Reporting and Recordkeeping Burden
The burden is approved under the
OMB control numbers stated in Table 2.
TABLE 2—ESTIMATED ANNUAL REPORTING AND RECORDKEEPING BURDEN
OMB control
No.
Respondents
Responses
Burden per
response
(hours)
0938–0147
0938–0146
0938–1012
0938–1012
0938–0974
0938–0994
0938–1012
........................
10
10
34
34
34
36
34
........................
120
20
1,360
1,360
34
2 18,000
1,360
........................
8
24
393.875
393.875
840
1
393.875
........................
Regulation section(s)
§ 431.812
§ 431.814
§ 431.978
§ 431.980
§ 431.992
..............................................................................
..............................................................................
..............................................................................
..............................................................................
..............................................................................
Total ..............................................................................
Total annual
burden
(hours)
1 960
480
535,670
1 535,670
28,560
23,400
3 535,670
589,070
1 We
are submitting a revision of the currently approved ICR for the proposed information collection requirements in this section of the regulation.
2 The currently approved number of responses is 23,400; however, the value is incorrect due to an arithmetic error. We have already submitted
an 83–C Change Worksheet to OMB to correct the error.
3 For the purpose of totaling the burden associated with the ICRs in this regulation, the annual burden associated with OMB control number
0938–1012 is counted only once.
If you comment on these information
collection and recordkeeping
requirements, please do either of the
following:
1. Submit your comments
electronically as specified in the
ADDRESSES section of this proposed rule;
or
2. Submit your comments to the
Office of Information and Regulatory
Affairs, Office of Management and
Budget,
Attention: CMS Desk Officer, [CMS–
6150–P].
Fax: (202) 395–6974; or
E-mail:
OIRA_submission@omb.eop.gov.
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V. Response to Comments
Because of the large number of public
comments we normally receive on
Federal Register documents, we are not
able to acknowledge or respond to them
individually. We will consider all
comments we receive by the date and
time specified in the DATES section of
this preamble, and, when we proceed
with a subsequent document, we will
respond to the comments in the
preamble to that document.
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VI. Regulatory Impact Analysis
A. Overall Impact
We have examined the impacts of this
rule as required by Executive Order
12866 on Regulatory Planning and
Review (September 30, 1993, as further
amended), the Regulatory Flexibility
Act (RFA) (September 19, 1980, Pub. L.
96–354), section 1102(b) of the Social
Security Act, section 202 of the
Unfunded Mandates Reform Act of 1995
(Pub. L. 104–4), Executive Order 13132
on Federalism (August 4, 1999), and the
Congressional Review Act (5 U.S.C.
804(2)).
Executive 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). For the reasons discussed
below, we have determined that this
proposed rule is not a major rule.
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1. Federal Contracting Cost Estimate
We have estimated that it will cost
$14.7 million annually for engaging
Federal contractors to review FFS and
managed care claims and calculate error
rates in 34 State programs (17 States for
Medicaid and 17 States for CHIP). We
estimated these costs as follows:
In the August 31, 2007 final rule, we
estimated the Federal cost for use of
Federal contractors conducting the FFS
and managed care measurements to be
$19.8 million annually. Due to more
recent data acquired through our
experience with Federal contractors in
the FY 2007, FY 2008, and FY 2009
PERM cycles, we were able to produce
a more accurate estimate by taking the
average of Federal contracting costs for
the three cycles and including
anticipated future PERM cycle costs.
The error rate measurements for 34 State
programs (17 States for Medicaid and 17
States for CHIP) would cost
approximately $14,682,777 in Federal
funds for the Federal contracting cost.
2. State Cost Estimate for Fee-for-Service
and Managed Care Reviews
We estimated that total State cost for
FFS and managed care reviews for 34
State programs is $6.2 million
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($4,309,490 in Federal cost and
$1,846,924 in State cost). This cost
estimate is based on the cost for States
to prepare and submit claims universe
information for both FFS and managed
care payments, prepare and submit
claims details and provider information
for sampled records, submit State
program policies and updates on a
quarterly basis, cooperate with Federal
contractors during data processing
review, participate in the difference
resolution and appeals process, and
prepare and submit a corrective action
plan for claims errors. These costs are
estimated as follows:
We estimated that the annualized
number of hours required to respond to
requests for required claims information
for FFS and managed care review for 34
State programs will be 112,200 hours
(3,300 hours per State per program). At
the 2009 general schedule GS–12–01
rate of pay that includes fringe and
overhead costs ($54.87/hour), we
calculated a cost of $6,156,414
($4,309,490 in Federal cost and
$1,846,924 in State cost). This cost
estimate includes the following
estimated annualized hours: (1) Up to
1,800 hours required for States to
develop and submit required claims and
capitation payments information; (2) up
to 500 hours for the collection and
submission of policies; and (3) up to
1,000 hours for States to cooperate with
CMS and the Federal contractors on
other aspects of the claims review and
corrective action process.
Therefore, the total annual estimate of
the State cost for 34 State programs to
submit information for FFS and
managed care reviews and participate
with CMS and Federal contractors is
$6,156,414 ($4,309,490 in Federal cost
and $1,846,924 in State cost).
3. Cost Estimate for Eligibility Reviews
Beginning in FY 2007, States review
eligibility in the same year they are
selected for FFS and managed care
reviews in Medicaid and CHIP. We
estimated that total cost for eligibility
review for 34 State programs is
$24,588,344 ($17,211,841 in Federal
cost and $7,376,503 in State cost). This
cost estimate is based on the cost for
States to submit information to CMS
and the cost for States to conduct
eligibility reviews and report rates to
CMS. These costs are estimated as
follows:
We estimated in the information
collection section, that the annualized
number of hours required to respond to
requests for information for the
eligibility review (for example, sampling
plan, monthly sample lists, the
eligibility corrective action report) for
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34 State programs will be 108,800 hours
(3,200 hours per State per program). At
the 2009 general schedule GS–12–01
rate of pay that includes fringe and
overhead costs ($54.87/hour), we
calculated a cost of $5,969,856
($4,178,899 in Federal cost and
$1,790,957 in State cost). This cost
estimate includes the following
estimated annualized hours: (1) Up to
1,000 hours required for States to
develop and submit a sampling plan; (2)
up to 1,200 hours for States to submit
12 monthly sample lists detailing the
cases selected for review; and (3) up to
1,000 hours for States to submit a
corrective action plan for purposes of
reducing the eligibility payment error
rate. For the eligibility review and
reporting of the findings, we estimated
that each State would need to review an
annual sample size of 504 active cases
to achieve a 3 percent margin of error
at a 95 percent confidence interval level
in the State-specific error rates. We also
estimated that States would need to
review 204 negative cases to produce a
case error rate that met similar
standards for statistical significance. We
estimated that for 34 State programs the
annualized number of hours required to
complete the eligibility case reviews
and report the eligibility-based error
data to CMS would be 339,320 hours
(9,980 hours per State, per program). At
the 2009 general schedule GS–12–01
rate of pay that includes fringe and
overhead costs ($54.87/hour), we
calculated a cost of $18,618,488
($13,032,942 in Federal cost and
$5,585,547 in State cost).
Therefore, the total annual estimate of
the cost for 34 State programs to submit
information and to conduct the
eligibility reviews and report the error
rate to CMS is $24,588,344 ($17,211,841
in Federal cost and $7,376,503 in State
cost).
The CHIPRA requires CMS to provide
States in their PERM year the option to
use PERM data to meet the MEQC
requirements described in section
1903(u) of the Act, and the option to use
MEQC data described in § 431.812 to
meet the PERM eligibility review
requirement. While the intent is to
reduce redundancies and cost burden
between the two programs and their
review requirements, States that
substitute findings may incur more costs
to implement changes to their PERM or
MEQC sampling and review procedures.
4. Cost Estimate for Total PERM Costs
Based on our estimates of the costs for
the FFS, managed care and eligibility
reviews for both the Medicaid and CHIP
programs at approximately $45.4
million ($36,204,108 in Federal cost and
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$9,223,428 in State cost), this rule does
not exceed the $100 million or more in
any 1 year criterion for a major rule, and
a regulatory impact analysis is not
required.
The RFA requires agencies to analyze
options for regulatory relief of small
businesses, if a rule has a significant
impact on a substantial number of small
entities. The great majority of hospitals
and most other health care providers
and suppliers are small entities, either
by being nonprofit organizations or by
meeting the SBA definition of a small
business (having revenues of less than
$7.0 million to $34.5 million in any 1
year). Individuals and States are not
included in the definition of a small
entity.
Providers could be required to supply
medical records or other similar
documentation that verified the
provision of Medicaid or CHIP services
to beneficiaries as part of the PERM
reviews, but we anticipate this action
would not have a significant cost impact
on providers. Providers would only
need to provide medical records for the
FFS component of this program. A
request for medical documentation to
substantiate a claim for payment would
not be a burden to providers nor would
it be outside the customary and usual
business practices of Medicaid or CHIP
providers. Not all States would be
reviewed every year and medical
records would only be requested for FFS
claims, so it is unlikely for a provider
to be selected more than once per
program per measurement cycle to
provide supporting documentation,
particularly in States with a large
Medicaid or CHIP managed care
population. If a provider is, in fact,
selected more than once per program to
provide supporting documentation it
would not be outside customary and
usual business practices.
In addition, the information should be
readily available and the response
should take minimal time and cost since
the response would merely require
gathering the documents and either
copying and mailing them or sending
them by facsimile. The request for
medical documentation from providers
is within the customary and usual
business practice of a provider who
accepts payment from an insurance
provider, whether it is a private
organization, Medicare, Medicaid, or
CHIP and should not have a significant
impact on the provider’s operations.
Therefore, the Secretary has determined
that this proposed 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
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impact analysis if a rule may have a
significant impact on the operations of
a substantial number of small rural
hospitals. This analysis must conform to
the provisions of section 603 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.
These entities may incur costs due to
collecting and submitting medical
records to the contractor to support
medical reviews; but, like any other
Medicaid or CHIP provider, we estimate
these costs would not be outside the
limit of usual and customary business
practices. Also, since the sample is
randomly selected and only FFS claims
are subject to medical review, we do not
anticipate that a great number of small
rural hospitals would be asked for an
unreasonable number of medical
records. As stated before, a State will be
reviewed only once, per program, every
3 years and it is unlikely for a provider
to be selected more than once per
program to provide supporting
documentation. Therefore, the Secretary
has determined that this proposed rule
would 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 (UMRA)
also requires that agencies assess
anticipated costs and benefits before
issuing any rule whose mandates
require spending in any 1 year of $100
million in 1995 dollars, updated
annually for inflation. In 2009, that
threshold is approximately $133
million. This proposed rule does not
impose costs on States to produce the
error rates for FFS and managed care
payments, but requires States and
providers to submit claims information
and medical records and cooperate with
Federal contractors during the review so
that error rates can be calculated.
Based on our estimates of State
participation burden for both Medicaid
and CHIP, for 34 States (17 States per
Medicaid and 17 States for CHIP), we
calculated that the annual burden for
these States for the PERM program is
approximately $9,223,428 in State costs
for both Medicaid and CHIP. The
combined costs of both programs total
approximately $542,555 for each of the
17 States. Thus, we do not anticipate
State costs to exceed $133 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
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otherwise has Federalism implications.
This proposed rule requires States to
prepare and submit claims universe
information for both FFS and managed
care payments, prepare and submit
claims details and provider information
for sampled records, submit State
program policies and updates on a
quarterly basis, cooperate with Federal
contractors during data processing
reviews, participate in the difference
resolution and appeals process, and
prepare and submit a corrective action
plan for claims errors. We estimated that
the burden to respond to requests for
claims information for the FFS and
managed care measurement for
Medicaid and CHIP for 34 State
programs (17 States for Medicaid and 17
States for CHIP) will be $6,156,414
($4,309,490 in Federal cost and
$1,846,924 in State cost).
This proposed rule also require States
selected for review to submit an
eligibility sampling plan, monthly
sample selection information, summary
review findings, State error rate data,
and other information in order for CMS
to calculate the eligibility State-specific
and national error rates. We estimated
that the burden to conduct the eligibility
measurement for Medicaid and CHIP for
34 State programs (17 States for
Medicaid and 17 States for CHIP) will
be approximately $24,588,344
($17,211,841 in Federal cost and
$7,376,503 in State cost). As a result, we
assert that this regulation will not have
a substantial impact on State or local
governments.
B. Anticipated Effects
This proposed rule is intended to
measure improper payments in
Medicaid and CHIP. States would
implement corrective actions to reduce
the error rate, thereby producing savings
over time. These savings cannot be
estimated until after the corrective
actions have been monitored and
determined to be effective, which can
take several years.
C. Alternatives Considered
This proposed rule reflects changes
required by the CHIPRA. Therefore, we
considered only applying additional
changes to the CHIP component of
PERM (except in instances where
CHIPRA specifically requires the
provision to apply to Medicaid and
CHIP). However, in order to maintain a
consistent measurement process for the
Medicaid and CHIP programs, we did
not choose this alternative. No other
alternatives were considered since the
modifications were required by Federal
statute.
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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
42 CFR Part 431
Grant programs—health, Health
facilities, Medicaid, Privacy, Reporting
and recordkeeping requirements.
42 CFR Part 447
Accounting, Administrative practice
and procedure, Drugs, Grant programs—
health, Health facilities, Health
professions, Medicaid, Reporting and
recordkeeping requirements, Rural
areas.
42 CFR Part 457
Administrative practice and
procedure, Grant programs—health,
Health insurance, Reporting and
recordkeeping requirements.
For the reasons set forth in the
preamble, the Centers for Medicare &
Medicaid Services proposes to amend
42 CFR chapter IV as set forth below:
PART 431—STATE ORGANIZATION
AND GENERAL ADMINISTRATION
1. The authority for part 431
continues to read as follows:
Authority: Sec. 1102 of the Social Security
Act, (42 U.S.C. 1302).
Subpart P—Quality Control
2. In 42 CFR part 431, revise all
references to ‘‘SCHIP’’ to read ‘‘CHIP’’.
3. Amend § 431.636 by revising all
references to ‘‘State Children’s Health
Insurance Program’’ to read ‘‘Children’s
Health Insurance Program.’’
4. Section 431.806 is amended by—
A. Redesignating paragraph (b) as
paragraph (c).
B. Adding new paragraph (b).
C. Revising redesignated paragraph
(c).
The addition and revision read as
follows:
§ 431.806
State plan requirements.
*
*
*
*
*
(b) Use of PERM data. A State plan
must provide for operating a Medicaid
eligibility quality control program that
is in accordance with § 431.978 through
§ 431.980 of this part to meet the
requirements of § 431.810 through
§ 431.822 of this subpart when a State
is in their PERM year.
(c) Claims processing assessment
system. Except in a State that has an
approved Medicaid Management
Information System (MMIS) under
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subpart C of part 433 of this subchapter,
a State Plan must provide for operating
a Medicaid quality control claims
processing assessment system that
meets the requirements of § 431.836 of
this subpart.
5. Section 431.812 is amended by
adding new paragraphs (f) and (g) to
read as follows:
§ 431.812
Review procedures.
*
*
*
*
*
(f) MEQC pilot reviews and waivers.
(1) A State may elect to conduct MEQC
pilot reviews using an alternative
methodology or a focused Medicaid
population with CMS approval.
(2) States must submit a pilot
proposal at least 60 days before planned
implementation of the pilot reviews.
(3) The State must receive CMS
approval of its plan before it is
implemented.
(g) Substitution of PERM data. A State
in its Payment Error Rate Measurement
(PERM) year may elect to substitute the
random sample of selected cases,
eligibility review findings, and payment
review findings obtained through PERM
reviews conducted in accordance with
§ 431.980 of this part for data required
in this section, if the only exclusions are
those set forth in § 431.978(d)(1) of this
part.
6. Section 431.814 is amended by
revising paragraph (c)(4) to read as
follows:
§ 431.814
Sampling plan and procedures.
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*
*
*
*
*
(c) * * *
(4) States must exclude from the
MEQC universe all of the following:
(i) SSI beneficiaries whose eligibility
determinations were made exclusively
by the Social Security Administration
under an agreement under section 1634
of the Act.
(ii) Individuals in foster care or
receiving adoption assistance whose
eligibility is determined under Title IV–
E of the Act.
(iii) Individuals receiving Medicaid
under programs that are 100 percent
Federally-funded.
(iv) Individuals whose eligibility was
determined under a State’s option under
section 1902(e)(13) of the Act.
*
*
*
*
*
Subpart Q—Requirements for
Estimating Improper Payments in
Medicaid and CHIP
7. Amend § 431.950 by revising the
reference to ‘‘State Children’s Health
Insurance Program’’ to read ‘‘Children’s
Health Insurance Program.’’
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8. Section § 431.954 is amended by
adding a sentence to the end of
paragraph (a) to read as follows:
§ 431.954
Basis and scope.
(a) * * * This subpart also
implements the provisions of section
601 of the Children’s Health Insurance
Program Reauthorization Act of 2009
(CHIPRA) (Pub. L. 111–3) which
requires that the new PERM regulations
include the following: Clearly defined
criteria for errors for both States and
providers; clearly defined processes for
appealing error determinations; clearly
defined responsibilities and deadlines
for States in implementing any
corrective action plans; requirements for
State verification of an applicant’s selfdeclaration or self-certification of
eligibility for, and correct amount of,
medical assistance under Medicaid or
child health assistance under CHIP; and
State-specific sample sizes for
application of the PERM requirements.
*
*
*
*
*
9. Section 431.958 is amended by—
A. Adding definitions for the terms
‘‘Annual sample size,’’ ‘‘Children’s
Health Insurance Program,’’ ‘‘Provider
error,’’ and ‘‘State error’’ in alphabetical
order.
B. Removing the definition of ‘‘State
Children’s Health Insurance Program.’’
C. Revising the definition of ‘‘Case’’.
The additions and revision read as
follows:
§ 431.958
Definitions and use of terms.
*
*
*
*
*
Annual sample size means the
number of fee-for-service claims,
managed care payments or eligibility
cases necessary to meet precision
requirements in a given PERM cycle.
*
*
*
*
*
Case means an individual beneficiary
or family enrolled in Medicaid or CHIP
or who has been denied enrollment or
has been terminated from Medicaid or
CHIP.
*
*
*
*
*
Children’s Health Insurance Program
(CHIP) means the program authorized
and funded under Title XXI of the Act.
*
*
*
*
*
Provider error includes, but is not
limited to one of the following:
(1) An improper payment made due to
lack of or insufficient documentation.
(2) Incorrect coding.
(3) Improper billing (for example,
unbundling, incorrect number of units).
(4) A payment that is in error due to
lack of medical necessity.
(5) Evidence that the service was not
provided in compliance with
documented State or Federal policy.
*
*
*
*
*
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State error includes, but is not limited
to one of the following:
(1) A payment that is in error due to
incorrect processing (for example,
duplicate of an earlier payment,
payment for a non-covered service,
payment for an ineligible beneficiary).
(2) Incorrect payment amount (for
example, incorrect fee schedule or
capitation rate applied, incorrect third
party liability applied).
(3) A payment error resulting from
services being provided to an individual
who—
(i) Was ineligible when authorized or
when he or she received services;
(ii) Was eligible for the program but
was ineligible for certain services he or
she received; or
(iii) Had not met applicable
beneficiary liability requirements when
authorized eligible or paid too much
toward actual liability.
*
*
*
*
*
10. Section 431.960 is added to read
as follows:
§ 431.960
Types of payment errors.
(a) General rule. State or provider
errors identified for the Medicaid and
CHIP improper payments measurement
under the Improper Payments
Information Act of 2002 must affect
payment under applicable Federal
policy and State policy.
(b) Data processing errors. (1) A
processing error is an error resulting in
an overpayment or underpayment that
is determined from a review of the claim
and other information available in the
State’s Medicaid Management
Information System, related systems, or
outside sources of provider verification.
(2) The difference in payment
between what the State paid (as
adjusted within improper payment
measurement guidelines) and what the
State should have paid is the dollar
measure of the payment error.
(c) Medical review errors. (1) A
medical review error is an error
resulting in an overpayment or
underpayment that is determined from
a review of the provider’s
documentation, the State’s written
policies, and a comparison with the
information presented on the claim.
(2) The difference in payment
between what the State paid (as
adjusted within improper payment
measurement guidelines) and what the
State should have paid is the dollar
measure of the payment error.
(d) Eligibility errors. (1) An eligibility
error is an error resulting from services
being provided to an individual who—
(i) Was ineligible when authorized or
when he or she received services;
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(ii) Was eligible for the program but
was ineligible for certain services he or
she received;
(iii) Had not met applicable
beneficiary liability requirements when
authorized as eligible or paid too much
toward actual liability; or
(iv) Had a lack of or insufficient
documentation in the case record to
make a definitive determination of
eligibility or ineligibility.
(2) The dollars paid in error due to the
eligibility error is the measure of the
payment error.
(3) A State eligibility error does not
result from the State’s verification of an
applicant’s self-declaration or selfcertification of eligibility for, and the
correct amount of, medical assistance or
child health assistance, if the State
process for verifying an applicant’s selfdeclaration or self-certification satisfies
the requirements for such process
applicable under regulations at
§ 457.380 of this chapter, in CMS
approved State plans, or otherwise
approved by the Secretary.
Requirements for acceptable selfdeclaration for eligibility reviews are
described at § 431.980(d)(1) and (d)(2).
(4) Negative case errors are errors
resulting from either of the following:
(i) Applications for Medicaid or CHIP
that are improperly denied by the State.
(ii) Existing cases that are improperly
terminated from Medicaid or CHIP by
the State.
(5) No payment errors are associated
with negative cases.
(e) Errors for purposes of determining
the national error rates. The Medicaid
and CHIP national error rates include
but are not limited to the errors
described in paragraphs (b) through
(d)(1) of this section.
(f) Errors for purposes of determining
the State error rates. (1) The Medicaid
and CHIP State error rates include but
are not limited to, the errors described
in paragraphs (b) through (d)(1)(iii) of
this section.
(2) Undetermined cases, as described
in paragraph (d)(1)(iv) of this section,
cited in the eligibility reviews are
excluded from State-specific payment
error rates if the errors satisfy the
criteria in paragraph (d)(3) of this
section.
(g) Error codes. CMS may define
different types of errors within the
above categories for analysis and
reporting purposes. Only dollars in error
will factor into a State’s PERM error
rate.
11. Section 431.970 is amended by
revising paragraph (a)(1) to read as
follows:
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§ 431.970 Information submission
requirements.
(a) * * *
(1) Adjudicated fee-for-service (FFS)
or managed care claims information or
both, on a quarterly basis, from the
review year;
*
*
*
*
*
12. Section 431.972 is added to read
as follows:
§ 431.972
Claims sampling procedures.
(a) Claims universe. The PERM claims
universe includes payments that were
originally paid (paid claims) and for
which payment was requested but
denied (denied claims) during the
Federal fiscal year, and for which there
is Federal financial participation (FFP)
(or would have been if the claim had not
been denied) through Title XIX
(Medicaid) or Title XXI (CHIP).
(b) Sample size. CMS estimates a
State’s annual sample size for claims
review at the beginning of the PERM
cycle.
(1) Precision and confidence levels.
The annual sample size must be
estimated to achieve a State-level error
rate within a 3 percent precision level
at 95 percent confidence interval for the
claims component of the PERM
program, unless the precision
requirement is waived by CMS on its
own initiative.
(2) Base year sample size. The annual
sample size in a State’s first PERM cycle
(the ‘‘base year’’) is—
(i) Five hundred fee-for-service claims
and 250 managed care payments drawn
from the claims universe; or
(ii) If the claims universe of fee-forservice claims or managed care
capitation payments from which the
annual sample is drawn is less than
10,000, the State may request to reduce
its sample size by the finite population
correction factor for the relevant PERM
cycle.
(3) Subsequent year sample size. In
PERM cycles following the base year:
(i) CMS considers the error rate from
the State’s previous PERM cycle to
determine the State’s annual sample
size for the current PERM cycle.
(ii) The maximum sample size is
1,000 fee-for-service or managed care
payments, respectively.
(iii) If a State measured in the FY
2007 or FY 2008 cycle elects to reject its
State-specific CHIP PERM rate
determined during those cycles,
information from those cycles will not
be used to calculate its annual sample
size in subsequent PERM cycles and the
State’s annual sample size in FY 2010
or FY 2011 is 500 fee-for-service and
250 managed care payments.
13. Section 431.978 is amended by—
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A. Revising paragraphs (a) through (c).
B. Revising paragraphs (d)(1)(i) and
(ii).
The revisions read as follows:
§ 431.978 Eligibility sampling plan and
procedures.
(a) Plan approval. For each review
year, the State must—
(1) Submit its Medicaid or CHIP
sampling plan (or revisions to a current
plan) for both active and negative cases
to CMS for approval by the August 1
before the review year; and
(2) Have its sampling plan approved
by CMS before the plan is implemented.
(b) Maintain current plan. The State
must do the both of the following:
(1) Keep its plan current, for example,
by making adjustments to the plan when
necessary due to fluctuations in the
universe.
(2) Review its plan each review year.
If it is determined that the approved
plan is—
(i) Unchanged from the previous
review year, the State must notify CMS
that it is using the plan from the
previous review year; or
(ii) Changed from the previous review
year, the State must submit a revised
plan for CMS approval.
(c) Sample size. (1) Precision and
confidence levels. Annual sample size
for eligibility reviews must be estimated
to achieve within a 3 percent precision
level at 95 percent confidence interval
for the eligibility component of the
program.
(2) Base year sample size. Annual
sample size for each State’s base year of
PERM is—
(i) Five hundred and four active cases
and 204 negative cases drawn from the
active and negative universes; or
(ii) If the active case universe or
negative case universe of Medicaid or
CHIP beneficiaries from which the
annual sample is drawn is less than
10,000, the sample size may be reduced
by the finite population correction
factor for the relevant PERM cycle.
(3) Subsequent year sample size. In
PERM cycles following the base year the
annual sample size may increase or
decrease based on the State’s prior
results of the previous cycle PERM error
rate information. The State may provide
information to CMS in the eligibility
sampling plan due to CMS by the
August 1 prior to the start of the fiscal
year to support the calculation of a
reduced annual sample size for the next
PERM cycle.
(i) CMS considers the error rate from
the State’s previous PERM cycle to
determine the State’s annual sample
size for the current PERM cycle.
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(ii) The maximum sample size is
1,000 for the active cases and negative
cases, respectively.
(iii) If the active case universe or
negative case universe of Medicaid or
CHIP beneficiaries from which the
annual sample is drawn is less than
10,000, the sample size may be reduced
by the finite population correction
factor for the relevant PERM cycle.
(iv) If a State measured in the FY 2007
or FY 2008 cycle elects to reject its
PERM CHIP rate as determined during
those cycles, information from those
cycles is not used to calculate the State’s
sample size in subsequent PERM cycles
and the State’s sample size in FY 2010
or FY 2011 is 504 active cases and 204
negative cases.
(d) * * *
(1) * * *
(i) Medicaid. (A) The Medicaid active
universe consists of all active Medicaid
cases funded through Title XIX for the
sample month.
(B) The following types of cases are
excluded from the Medicaid active
universe:
(1) Cases for which the Social
Security Administration, under a
section 1634 agreement with a State,
determines Medicaid eligibility for
Supplemental Security Income
recipients.
(2) All foster care and adoption
assistance cases under Title IV–E of the
Act are excluded from the universe in
all States.
(3) Cases under active fraud
investigations.
(4) Cases in which eligibility was
determined under section 1902(e)(13) of
the Act for States’ express lane option.
(C) If the State cannot identify cases
under active fraud investigations for
exclusion from the universe previous to
the sample selection, the State shall
drop these cases from review if they are
selected in the sample and are later
determined to be under active fraud
investigation at the time of selection.
(ii) CHIP. (A) The CHIP active
universe consists of all active case CHIP
and Title XXI Medicaid expansion cases
that are funded through Title XXI for the
sample month.
(B) The following types of cases are
excluded from the CHIP active universe:
(1) Cases under active fraud
investigation.
(2) Cases in which eligibility was
determined under section 1902(e)(13) of
the Act for States’ express lane option.
(C) If the State cannot identify cases
that meet the exclusion criteria
specified in paragraph (d)(1)(ii)(B) of
this section before sample selection, the
State must drop these cases from review
if is later determined that the cases meet
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the exclusion criteria specified in
paragraph (d)(1)(ii)(B) of this section.
*
*
*
*
*
14. Section 431.980 is amended by—
A. Revising the introductory text of
paragraph (d)(1).
B. In paragraph (d)(1)(i) and (ii),
removing the ‘‘;’’ at the end of the
paragraph and adding in its place a ‘‘.’’.
C. Revising paragraph (d)(1)(iii).
D. Redesignating paragraph (d)(1)(vi)
as (d)(1)(x).
D. Adding new paragraphs (d)(1)(vi)
through (d)(1)(ix).
E. Revising the introductory text of
newly redesignated paragraph (d)(1)(x).
F. Revising the introductory text of
paragraph (d)(2).
G. Adding paragraph (f).
The revisions and additions read as
follows:
§ 431.980
Eligibility review procedures.
*
*
*
*
*
(d) * * *
(1) Active cases—Medicaid. Unless
the State has selected to substitute
MEQC data for PERM data under
paragraph (f) of this section, the agency
must complete all of the following:
*
*
*
*
*
(iii) Examine the evidence in the case
file that supports categorical and
financial eligibility for the category of
coverage in which the case is assigned,
and independently verify information
that is missing, older than 12 months
and likely to change, or otherwise as
needed, to verify eligibility.
*
*
*
*
*
(vi) Elements of eligibility in which
State policy allows for self-declaration
can be verified with a new selfdeclaration statement.
(vii) The self-declaration must be—
(A) Present in the record;
(B) Not outdated (more than 12
months old);
(C) In a valid, State-approved format;
and
(D) Consistent with other facts in the
case record.
(viii) If a self-declaration statement in
the case record is more than 12 months
old, eligibility may be verified through
a new self-declaration statement or
other third party sources.
(ix) If eligibility or ineligibility cannot
be verified, cite a case as undetermined
as specified in paragraph (d)(1)(x)(B) or
(d)(2)(ii) of this section.
(x) As a result of paragraphs (d)(1)(i)
through (d)(1)(ix) of this section—
*
*
*
*
*
(2) Active cases—CHIP. In addition to
the procedures for active cases as set
forth in paragraphs (d)(1)(i) through
(d)(1)(ix) of this section, once the agency
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34485
establishes CHIP eligibility, the agency
must verify that the case is not eligible
for Medicaid by determining that the
child has income above the Medicaid
levels in accordance with the
requirements in § 457.350 of this
chapter. Upon verification, the agency
must—
*
*
*
*
*
(f) Substitution of MEQC data. (1) A
State in their PERM year may elect to
substitute the random sample of
selected cases, eligibility review
findings, and payment reviews findings
obtained through MEQC reviews
conducted in accordance with section
1903(u) of the Act for data required in
this section, as long as the State MEQC
reviews are based on a broad,
representative sample of Medicaid
applicants or enrollees in the State, if
the only exclusions are those set forth
in section 1902(e)(13) of the Act,
§ 431.814(c)(4), and § 431.978(d)(1) of
this part.
(2) MEQC samples must also meet
PERM confidence and precision
requirements.
15. Section 431.988 is amended by
revising paragraphs (b)(1) and (2) to read
as follows:
§ 431.988 Eligibility case review
completion deadlines and submittal of
reports.
*
*
*
*
*
(b) * * *
(1) Case and payment error data for
active cases.
(2) Case error data for negative cases.
*
*
*
*
*
16. Section 431.992 is revised to read
as follows:
§ 431.992
Corrective action plan.
(a) The State agency must develop a
corrective action plan designed to
reduce improper payments in its
Medicaid and CHIP programs based on
its analysis of the error causes in the
FFS, managed care, and eligibility
components.
(b) In developing a corrective action
plan, the State must take the following
actions:
(1) Data analysis. (i) States must
conduct data analysis such as reviewing
clusters of errors, general error causes,
characteristics, and frequency of errors
that are associated with improper
payments as well as error causes
associated with number of errors.
(ii) Data analysis may sort the
predominant payment errors and
number of errors by the following:
(A) Type: General classification (for
example, FFS, managed care,
eligibility).
(B) Element: Specific type of
classification (for example, no
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documentation errors, duplicate claims,
ineligible cases due to excess income).
(C) Nature: Cause of error (for
example, providers not submitting
medical records, lack of systems edits,
unreported changes in income that
caused ineligibility).
(iii) States must analyze active and
negative case errors and causes for
undetermined case findings under the
eligibility component.
(2) Program analysis. (i) States must
review the findings of the data analysis
to determine the specific programmatic
causes to which errors are attributed (for
example, provider lack of understanding
of the PERM requirement to provide
documentation) and to identify root
error causes.
(ii) The States may need to analyze
the agency’s operational policies and
procedures and identify those policies
or procedures, or both that are prone to
contribute to errors, for example,
unclear policies or lack of operational
oversight at the local level.
(3) Corrective action planning. States
must determine the corrective actions to
be implemented that address the root
error causes.
(4) Implementation and monitoring.
(i) States must develop an
implementation schedule for each
corrective action initiative and
implement those actions in accordance
with the schedule.
(ii) The implementation schedule
must identify the following:
(A) Major tasks;
(B) Key personnel responsible for
each activity; and
(C) A timeline for each action
including target implementation dates,
milestones, and monitoring.
(5) Evaluation. States must evaluate
the effectiveness of the corrective action
by assessing the following:
(i) Improvements in operations;
(ii) Efficiencies;
(iii) Number of errors; and
(iv) Improper payments.
(c) The State agency must submit to
CMS and implement the corrective
action plan for the fiscal year it was
reviewed no later than 60 calendar days
after the date on which the State’s
Medicaid or CHIP error rates are posted
on the CMS contractor’s Web site.
(d) The State must submit a new
corrective action plan for each
subsequent error rate measurement that
contains an update on the status of a
previous corrective action plan. Items to
address in the new corrective action
plan include, but are not limited to the
following:
(1) Effectiveness of implemented
corrective actions, as assessed using
concrete data.
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(2) Discontinued or ineffective
actions, actions not implemented, and
those actions, if any, that were
substituted for such discontinued,
ineffective, or abandoned actions.
(3) Findings on short-term corrective
actions.
(4) The status of the long-term
corrective actions.
17. Section 431.998 is amended by—
A. Revising the section heading as set
forth below.
B. Revising paragraphs (a) and (b).
C. Redesignating paragraph (c) as (d).
D. Adding new paragraph (c).
The revisions and addition read as
follows:
(2) After the filing of an appeals
request. (i) Any changes in error
findings must be reported to CMS by the
deadline for submitting final eligibility
review findings.
(ii) Any unresolved differences may
be addressed by CMS not less than 60
days and no more than 90 days after the
State submits its eligibility error data.
(iii) Any appeals of determinations
based on interpretations of Federal
policy may be referred to CMS.
(iv) If CMS’s decision causes an
erroneous payment finding to be made,
any resulting recoveries are governed by
§ 431.1002 of this subchapter.
*
*
*
*
*
§ 431.998
process.
PART 447—PAYMENTS FOR
SERVICES
Difference resolution and appeal
(a) The State may file, in writing, a
request with the Federal contractor to
resolve differences in the Federal
contractor’s findings based on medical
or data processing reviews on FFS and
managed care claims in Medicaid or
CHIP within 10 business days after the
disposition report of claims review
findings is posted on the contractor’s
Web site. The State must complete all of
the following:
(1) Have a factual basis for filing the
difference.
(2) Provide the Federal contractor
with valid evidence directly related to
the error finding to support the State’s
position that the claim was properly
paid.
(b) For a claim in which the State and
the Federal contractor cannot resolve
the difference in findings, the State may
appeal to CMS for final resolution
within 5 business days from the date of
the contractor’s finding as a result of the
difference resolution is posted on the
contractor’s Web site. There is no
minimum dollar threshold required to
appeal a difference in findings.
(c) For eligibility error determinations
made by agencies or personnel
functionally and physically separate
from the State agencies and personnel
that are responsible for Medicaid and
CHIP policy and operations, the State
may appeal error determinations by
filing an appeal request.
(1) Filing an appeal request. The State
may—
(i) File its appeal request with the
appropriate State agency; or
(ii) If no appeals process is in place
at the State level, differences in
findings—
(A) Must be documented in writing
for the independent State agency to
consider; or
(B) May be resolved at the State level
through document exchange facilitated
by CMS.
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18. The authority citation for part 447
continues to read as follows:
Authority: Sec. 1102 of the Social Security
Act (42 U.S.C. 1302).
19. In 42 CFR part 447, revise all
references to ‘‘SCHIP’’ to read ‘‘CHIP’’.
20. In § 447.504 amend paragraph
(g)(15) by revising the reference to
‘‘State Children’s Health Insurance
Program’’ to read ‘‘Children’s Health
Insurance Program.’’
PART 457—ALLOTMENTS AND
GRANTS TO STATES
21. The authority citation for part 457
continues to read as follows:
Authority: Section 1102 of the Social
Security Act (42 U.S.C. 1302).
22. In 42 CFR part 457, revise all
references to ‘‘SCHIP’’ to read ‘‘CHIP’’.
23. Section 457.10 is amended by—
A. Adding the definition of
‘‘Children’s Health Insurance Program’’
in alphabetical order.
B. Removing the definition of ‘‘State
Children’s Health Insurance Program.’’
The addition reads as follows:
§ 457.10
Definitions and use of terms.
*
*
*
*
*
Children’s Health Insurance Program
(CHIP) means a program established and
administered by a State, jointly funded
with the Federal government, to provide
child health assistance to uninsured,
low-income children through a separate
child health program, a Medicaid
expansion program, or a combination
program.
*
*
*
*
*
24. In 42 CFR part 457, revise all
references to ‘‘State Children’s Health
Insurance Program’’ to read ‘‘Children’s
Health Insurance Program.’’
Authority: (Catalog of Federal Domestic
Assistance Program No. 93.778, Medical
Assistance Program).
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Dated: April 14, 2009.
Charlene Frizzera,
Acting Administrator, Centers for Medicare
& Medicaid Services.
Approved: May 7, 2009.
Kathleen Sebelius,
Secretary.
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Agencies
[Federal Register Volume 74, Number 134 (Wednesday, July 15, 2009)]
[Proposed Rules]
[Pages 34468-34487]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-16538]
[[Page 34467]]
-----------------------------------------------------------------------
Part III
Department of Health and Human Services
-----------------------------------------------------------------------
Centers for Medicare & Medicaid Services
-----------------------------------------------------------------------
42 CFR Parts 431, 447, and 457
Medicaid Program and Children's Health Insurance Program (CHIP);
Revisions to the Medicaid Eligibility Quality Control and Payment Error
Rate Measurement Programs; Proposed Rule
Federal Register / Vol. 74, No. 134 / Wednesday, July 15, 2009 /
Proposed Rules
[[Page 34468]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Parts 431, 447, and 457
[CMS-6150-P]
RIN 0938-AP69
Medicaid Program and Children's Health Insurance Program (CHIP);
Revisions to the Medicaid Eligibility Quality Control and Payment Error
Rate Measurement Programs
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: This proposed rule would implement provisions from the
Children's Health Insurance Program Reauthorization Act of 2009
(CHIPRA) (Pub. L. 111-3) with regard to the Medicaid Eligibility
Quality Control (MEQC) and Payment Error Rate Measurement (PERM)
programs. This proposed rule would also codify several procedural
aspects of the process for estimating improper payments in Medicaid and
the Children's Health Insurance Program (CHIP).
DATES: To be assured consideration, comments must be received at one of
the addresses provided below, no later than 5 p.m. on August 14, 2009.
ADDRESSES: In commenting, please refer to file code CMS-6150-P. Because
of staff and resource limitations, we cannot accept comments by
facsimile (FAX) transmission.
You may submit comments in one of four ways (please choose only one
of the ways listed):
1. Electronically. You may submit electronic comments on this
regulation to https://www.regulations.gov. Follow the instructions for
``Comment or Submission'' and enter the filecode to find the document
accepting comments.
2. By regular mail. You may mail written comments (one original and
two copies) to the following address only:
Centers for Medicare & Medicaid Services, Department of Health and
Human Services, Attention: CMS-6150-P, P.O. Box 8020, Baltimore, MD
21244-8020.
Please allow sufficient time for mailed comments to be received
before the close of the comment period.
3. By express or overnight mail. You may send written comments (one
original and two copies) to the following address only:
Centers for Medicare & Medicaid Services, Department of Health and
Human Services, Attention: CMS-6150-P, Mail Stop C4-26-05, 7500
Security Boulevard, Baltimore, MD 21244-1850.
4. By hand or courier. If you prefer, you may deliver (by hand or
courier) your written comments (one original and two copies) before the
close of the comment period to either of the following addresses:
a. Room 445-G, Hubert H. Humphrey Building, 200 Independence Avenue,
SW., Washington, DC 20201.
(Because access to the interior of the Hubert H. Humphrey (HHH)
Building is not readily available to persons without Federal Government
identification, commenters are encouraged to leave their comments in
the CMS drop slots located in the main lobby of the building. A stamp-
in clock is available for persons wishing to retain a proof of filing
by stamping in and retaining an extra copy of the comments being
filed.)
b. 7500 Security Boulevard, Baltimore, MD 21244-1850.
If you intend to deliver your comments to the Baltimore address,
please call (410) 786-9994 in advance to schedule your arrival with one
of our staff members.
Comments mailed to the addresses indicated as appropriate for hand
or courier delivery may be delayed and received after the comment
period.
Submission of comments on paperwork requirements. You may submit
comments on this document's paperwork requirements by following the
instructions at the end of the ``Collection of Information
Requirements'' section in this document.
For information on viewing public comments, see the beginning of
the SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Elizabeth Lindner, (410) 786-7481, or
Jessica Woodard, (410) 786-9249.
SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All comments received before the
close of the comment period are available for viewing by the public,
including any personally identifiable or confidential business
information that is included in a comment. We post all comments
received before the close of the comment period on the following Web
site as soon as possible after they have been received: https://www.regulations.gov. Follow the search instructions on that Web site to
view public comments.
Comments received timely will also be available for public
inspection as they are received, generally beginning approximately 3
weeks after publication of a document, at the headquarters of the
Centers for Medicare & Medicaid Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday through Friday of each week from 8:30
a.m. to 4 p.m. To schedule an appointment to view public comments,
phone 1-800-743-3951.
I. Background
A. Medicaid Eligibility Quality Control Program
The Medicaid Eligibility Quality Control (MEQC) program is set
forth in section 1903(u) of the Social Security Act (the Act) and
requires States to report to the Secretary the ratio of States'
erroneous excess payments for medical assistance to total expenditures
for medical assistance. Section 1903(u) of the Act also sets a 3-
percent threshold for improper payments in any fiscal year and the
Secretary may withhold payments to States based on the amount of
improper payments that exceed the threshold.
B. The Improper Payments Information Act of 2002
The Improper Payments Information Act of 2002 (IPIA) (Pub. L. 107-
300, enacted on November 26, 2002) requires the heads of Federal
agencies to annually review programs they oversee to determine if they
are susceptible to significant erroneous payments. If any programs are
found to be susceptible to significant improper payments, then the
agency must estimate the amount of improper payments, report those
estimates to the Congress, and submit a report on actions the agency is
taking to reduce erroneous expenditures. The IPIA directed the Office
of Management and Budget (OMB) to provide guidance on implementation.
OMB defines ``significant erroneous payments'' as annual erroneous
payments in the program exceeding both 2.5 percent of program payments
and $10 million (OMB M-06-23, Appendix C to OMB Circular A-123, August
10, 2006). For those programs found to be susceptible to significant
erroneous payments, Federal agencies must provide the estimated amount
of improper payments and report on what actions the agency is taking to
reduce them, including setting targets for future erroneous payment
levels and a timeline by which the targets will be reached.
The Medicaid program and the Children's Health Insurance Program
(CHIP) were identified as programs at risk for significant erroneous
payments. The Department of Health and Human Services (DHHS) reports
the estimated
[[Page 34469]]
error rates for the Medicaid and CHIP programs in its annual
Performance and Accountability Report (PAR) to Congress.
C. Regulatory History
1. Medicaid Eligibility Quality Control Program
Sections 431.800 through 431.865 set forth the regulatory
requirements for States to conduct the annual MEQC measurement. A
Medicaid State Operations letter (93-58) dated July 23, 1993
implemented MEQC pilots that allowed States to conduct special studies
that would take the place of the ``traditional'' MEQC review. States
conducting pilot reviews are not subject to the threshold and
disallowance provisions under section 1903(u) of the Act as long as the
special studies continue.
Currently, the MEQC program consists of the following:
MEQC traditional--Operating MEQC under 42 CFR 431.800
through 431.865 and selecting a random sample of all Medicaid
applicants and enrollees and reviewing them under guidance in the State
Medicaid Manual.
MEQC pilots--Operating MEQC under a special study, a
target population and providing oversight to reduce and prevent errors
and improve program administration.
MEQC waivers--Operating MEQC as a part of a CMS approved
section 1115 waiver and reviewing beneficiaries included in the
research and demonstration project.
2. Payment Error Rate Measurement (PERM) Program
Section 1102(a) of the Act authorizes the Secretary to establish
such rules and regulations as may be necessary for the efficient
administration of the Medicaid and CHIP programs. The Medicaid statute
at section 1902(a)(6) of the Act and the CHIP statute at section
2107(b)(1) of the Act require States to provide information that the
Secretary finds necessary for the administration, evaluation, and
verification of the States' programs. Also, section 1902(a)(27) of the
Act (and Sec. 457.950 of the regulations) requires providers to submit
information regarding payments and claims as requested by the
Secretary, State agency, or both. Under the authority of these
statutory provisions, we published in the August 27, 2004 Federal
Register (69 FR 52620) a proposed rule to comply with the requirements
of the IPIA and the OMB guidance. The proposed rule set forth
provisions for all States to annually estimate improper payments in
their Medicaid and CHIP programs and to report the State-specific error
rates for purposes of our computing the national improper payment
estimates for these programs.
In the October 5, 2005 Federal Register (70 FR 58260), we published
an interim final rule with comment period (IFC). The IFC responded to
public comments on the proposed rule, and informed the public of our
national contracting strategy and of our plan to measure improper
payments in a subset of States. Our State selection process ensures
that a State is measured once, and only once, every 3 years for each
program.
In response to the public comments from the October 5, 2005 IFC, we
published a second IFC in the August 28, 2006 Federal Register (71 FR
51050), which reiterated our national contracting strategy to estimate
improper payments in both Medicaid and CHIP fee-for-service (FFS) and
managed care, and set forth and invited further comments on State
requirements for estimating improper payments due to errors in Medicaid
and CHIP eligibility determinations. We also announced that a State's
Medicaid and CHIP programs would be reviewed in the same year.
In the August 31, 2007 Federal Register (72 FR 50490), we published
a final rule for the PERM program, which implements the IPIA
requirements. The August 31, 2007 final rule responded to the public
comments on the August 28, 2006 IFC and finalized State requirements
for submitting claims to the Federal contractors that conduct FFS and
managed care reviews. The final rule also finalized State requirements
for conducting eligibility reviews and estimating payment error rates
due to errors in eligibility determinations.
D. Children's Health Insurance Program Reauthorization Act of 2009
On February 4, 2009, the Children's Health Insurance Program
Reauthorization Act of 2009 (CHIPRA) (Pub. L. 111-3) was enacted.
(Please note, as a result of this legislation, that the program
formerly known as the ``State Children's Health Insurance Program
(SCHIP)'' is now referred to as the ``Children's Health Insurance
Program (CHIP)''). Sections 203 and 601 of the CHIPRA relate to the
PERM program.
Section 203 of the CHIPRA establishes an error rate measurement
with respect to the enrollment of children under the express lane
eligibility option. The law directs States not to include children
enrolled using the express lane eligibility option in data or samples
used for purposes of complying with the MEQC and PERM requirements.
Provisions for States' express lane eligibility option will be set
forth in a future rulemaking document.
Section 601 of the CHIPRA provides for a 90 percent Federal match
for Children's Health Insurance Program (CHIP) spending related to PERM
administration and excludes such spending from the 10 percent
administrative cap. (Section 2105(c)(2) of the CHIP statute gives
States the ability to use an amount up to 10 percent of the CHIP
benefit expenditures for outreach efforts, additional services other
than the standard benefit package for low-income children, and
administrative costs.)
The CHIPRA requires a new PERM rule and delays any calculation of a
PERM error rate for CHIP until 6 months after the new PERM rule is
effective. Additionally, the CHIPRA provides that States that were
scheduled for PERM measurement in fiscal year (FY) 2007 may elect to
accept a CHIP PERM error rate determined in whole or in part on the
basis of data for FY 2007, or may elect instead to consider its PERM
measurement conducted for FY 2010 as the first fiscal year for which
PERM applies to the State for CHIP. Similarly, the CHIPRA provides that
States that were scheduled for PERM measurement in FY 2008 may elect to
accept a CHIP PERM error rate determined in whole or in part on the
basis of data for FY 2008, or may elect instead to consider its PERM
measurement conducted for FY 2011 as the first fiscal year for which
PERM applies to the State for CHIP.
The CHIPRA requires that the new PERM rule include the following:
Clearly defined criteria for errors for both States and
providers.
Clearly defined processes for appealing error
determinations.
Clearly defined responsibilities and deadlines for States
in implementing any corrective action plans.
Requirements for State verification of an applicant's
self-declaration or self-certification of eligibility for, and correct
amount of, medical assistance under Medicaid or child health assistance
under CHIP.
State-specific sample sizes for application of the PERM
requirements.
In addition, the CHIPRA aims to harmonize the PERM and MEQC
programs and provides States with the option to apply PERM data
resulting from its eligibility reviews for meeting MEQC requirements
and vice versa, with certain conditions.
[[Page 34470]]
E. CMS Response to the CHIPRA
As required by the CHIPRA, we are proposing revised MEQC and PERM
provisions in this proposed rule.
Section 601(b) of the CHIPRA states that ``the Secretary shall not
calculate or publish any national or State-specific error rate based on
the application of the payment error rate measurement (in this section
referred to as `PERM') requirements to CHIP until after the date that
is 6 months after the date on which a new final rule (in this section
referred to as the `new final rule') promulgated after the date of the
enactment of this Act and implementing such requirements in accordance
with the requirements of subsection (c) is in effect for all States.''
The CHIP error rate for the FY 2008 cycle was scheduled to be published
in the FY 2009 PAR (in November 2009), which is less than 6 months
after the expected promulgation and effective date of this new final
rule. Therefore, the publication of any CHIP error rates for FY 2008 is
delayed until at least 6 months after the final rule implementing the
CHIPRA requirements for PERM is effective.
As noted above, section 601(d) of the CHIPRA provides that States
that were scheduled for PERM measurement in FY 2007 may elect to accept
a CHIP PERM error rate determined in whole or in part on the basis of
data for FY 2007, or may elect instead to consider its PERM measurement
conducted for FY 2010 as the first fiscal year for which PERM applies
to the State for CHIP. In addition, the CHIPRA provides that States
that were scheduled for PERM measurement in FY 2008 may elect to accept
a CHIP PERM error rate determined in whole or in part on the basis of
data for FY 2008, or may elect instead to consider its PERM measurement
conducted for FY 2011 as the first fiscal year for which PERM applies
to the State for CHIP.
Accordingly, a State measured in the FY 2007 cycle that elects to
accept the PERM error rate for its CHIP program determined in whole or
in part on the basis of data for FY 2007 is required to notify CMS of
its intentions through an acceptance form provided to all States in a
State Health Official letter. Similarly, a State measured in the FY
2008 cycle that elects to accept the PERM error rate for its CHIP
program determined in whole or in part on the basis of data for FY 2008
is required to notify CMS of its intentions through an acceptance form
provided to all States in a State Health Official letter. If a State
measured in the FY 2007 or FY 2008 cycles elects to reject the CHIP
PERM rate determined during those cycles, they do not need to notify
CMS of this decision. However, information from those cycles will not
be used to calculate the State-specific sample sizes and CMS will rely
on the standard assumptions for determining sample size.
In order for section 601(d) of the CHIPRA to be read in harmony
with the IPIA, which requires a CHIP PERM error rate to be calculated
annually, we believe that the appropriate reading of section 601(d) of
the CHIPRA, construing the law as a whole and giving effect to all
language of the CHIPRA, is that a State may only elect to reject the
PERM error rate for the State's CHIP program for FY 2007 or FY 2008 and
instead have its PERM error rate for its CHIP program measured in FY
2010 or FY 2011, respectively. A State scheduled for PERM measurement
in FY 2008 will still have its PERM error rate for its Medicaid program
measured.
Additionally, States scheduled for PERM measurement in FY 2009 will
have the CHIP program reviewed and error rates calculated after the
final rule is in effect. Furthermore, the FY 2009 Medicaid measurement
is proceeding with no delays as a result of the CHIPRA, and FY 2009
Medicaid error rates will be calculated under the new final rule.
II. Provisions of the Proposed Regulations
As a result of the CHIPRA, we are proposing a nomenclature change
to parts 431, 447, and 457. The program formerly known as the ``State
Children's Health Insurance Program (SCHIP)'' is now referred to as the
``Children's Health Insurance Program (CHIP).'' We are also proposing
the following revisions to the current PERM provisions:
A. Sample Sizes
Section 601(f) of the CHIPRA requires us to establish State-
specific sample sizes for application of the PERM requirements with
respect to CHIP for fiscal years beginning with the first fiscal year
that begins on or after the date on which the new final rule is in
effect for all States, on the basis of such information as the
Secretary determines appropriate. In establishing such sample sizes,
the Secretary shall, to the greatest extent practicable: (1) Minimize
the administrative cost burden on States under Medicaid and CHIP; and
(2) maintain State flexibility to manage such programs.
To comply with the IPIA, the PERM program must estimate a national
Medicaid and a national CHIP error rate that covers the 50 States and
District of Columbia. Consistent with OMB's precision requirements
defined in its IPIA guidance, the estimated national error rate for
each program must be bound by a 90 percent confidence interval of 2.5
percentage points in either direction of the estimate. Since States
administer Medicaid and CHIP and make payments for services rendered
under the programs, we collect State-level information at a high level
of confidence (the estimated error rate for a State must be bound by a
95 percent confidence interval of 3 percentage points in either
direction). To estimate the national error rate, as well as State-
specific error rates, reviews are conducted in three areas for both the
Medicaid and CHIP programs: (1) Fee-for-service (FFS), (2) managed
care, and (3) program eligibility. The FFS and managed care reviews are
referred to jointly as the ``claims review,'' while the program
eligibility review is referred to as the ``eligibility review.''
Samples of payments made on a FFS and managed care basis for the
claims review and samples of beneficiaries for the eligibility review
are drawn each year in order to calculate a national error rate that
meets the precision requirements described in OMB Guidance (OMB M-06-
23, Appendix C to OMB Circular A-123, August 10, 2006). The preferred
method is to achieve the precision goal with the smallest sample size
possible, so as to reduce the staff burden on States, the Federal
government, beneficiaries, and providers. We determined that the most
efficient method, statistically, is to draw a sample of States and then
draw a sample of payments from the payments made by the sampled States.
The process for drawing a sample of States is described in detail in
the preamble to the August 31, 2007 final rule (72 FR 50490). We are
not proposing modifications to the current approach, which samples 17
States per year for a PERM measurement cycle. This rulemaking addresses
the State-specific sample sizes for samples of claims and beneficiaries
within a State.
In light of the new CHIPRA requirements, we are proposing to add
new Sec. 431.972, to describe more fully the claims sampling
procedures used for the claims review, as well as the process for
establishing State-specific sample sizes for PERM, although we note
that the execution of these responsibilities would remain with CMS and
the Federal contractors, not with the States. Under the Secretary's
authority at section 1102(a) of the Act and in order to effectively
implement the IPIA, we are also proposing that these sampling
[[Page 34471]]
procedures apply to both Medicaid and CHIP.
We are also proposing to revise Sec. 431.978 to provide additional
guidance on State Medicaid and CHIP eligibility sample sizes by
clarifying the process for establishing State-specific sample sizes.
1. Fee-for-Service (FFS) and Managed Care
a. Universe Definition
In order to implement the IPIA and related requirements (OMB M-06-
23, Appendix C to OMB Circular A-123, August 10, 2006) that require
Federal agencies to estimate the amount of improper payments in
programs with significant erroneous payments (which includes Medicaid
and CHIP), in the current Sec. 431.970(a)(1) we require States to
submit ``[a]ll adjudicated fee-for-service (FFS) and managed care
claims information, on a quarterly basis, from the review year,'' so
that a sample of payments can be reviewed and from the review findings
CMS can estimate the amount of improper payments in each program. We
propose to remove the word ``all'' from Sec. 431.970(a)(1) because
certain types of payments are excluded from PERM sampling and review
for technical reasons. This requirement has been further clarified
through instructions issued by CMS to the States.
For the PERM claims review component, the ``claims universe'' is
defined in the new Sec. 431.972 as including payments that were
originally paid (paid claims) and for which payment was requested but
denied (denied claims) during the Federal fiscal year, and for which
there was Federal financial participation (FFP) (or would have been if
the claim had not been denied) through Title XIX of the Act (Medicaid)
or Title XXI of the Act (CHIP). Depending on the context in which it is
used, the claims universe may refer to either all of the adjudicated
FFS claims during the fiscal year under review, or all of the managed
care capitation payments made during the fiscal year under review, for
Medicaid or CHIP.
Due to the significant variation in State systems for processing,
paying, and claiming reimbursement for medical services under Medicaid
and CHIP, we are not proposing to include a more specific claims
universe description in regulation. Rather, States should refer to more
detailed claims universe specifications that will be published by CMS
in separate instructions at the beginning of each PERM measurement
cycle. However, we are proposing that States must establish controls to
ensure that the FFS, managed care, and eligibility universes are
complete and accurate. For example, this would include the comparisons
between the PERM universes and the State's CMS-64 and CMS-21 financial
reports.
b. Stratification
In FY 2006, we measured only the error rate for the FFS component
of Medicaid. To obtain the required precision levels while minimizing
the sample size, and therefore reducing the burden on States, the
claims universe for FFS payments for Medicaid was stratified by service
category and a stratified random sample was drawn for each State. In FY
2007 and beyond, we measure the error rates for Medicaid FFS, Medicaid
managed care, CHIP FFS, and CHIP managed care separately (to the extent
that a State has each of these programs). We also stratify each
universe by dollars rather than service category.
Under this stratification and sampling approach, all payments in
each universe are sorted from largest to smallest payment amounts. The
payments are then divided into strata such that the total payments in
each stratum are the same. For example, if five strata are used, the
total dollars in each stratum would equal 20 percent of the total
dollars in the universe. The first stratum would contain the highest
dollar-valued payments, and the last stratum would contain the smallest
dollar-valued payments, including all zero-paid and denied claims
(denials have a zero dollar amount, and therefore, would appear in the
stratum with the smallest dollar values). An equal number of FFS claims
or managed care payments are then drawn from each stratum, which means
the sample would include proportionately more high-dollar payments and
proportionately fewer low-dollar payments and denials, compared to
their representation in the universe. This overweighting of higher-
dollar payments (which is taken into account when calculating error
rates) enables us to draw a smaller sample size that has a reasonable
probability of meeting the precision requirements, compared to a
perfectly random sample or a sample stratified by service type. In this
manner, we reduce burden on States, the Federal government,
beneficiaries, and providers.
c. Fee-for-Service and Managed Care Sample Size
In order to establish State-specific sample sizes, we are proposing
that the annual sample size in a State's first PERM cycle (referred to
as ``initial sample'' or ``base sample'') would be 500 FFS claims and
250 managed care payments.
We determined this initial sample size based on the experience of
the PERM pilot study and our requirement that the estimated error rate
for a State must be bound by a 95 percent confidence interval of 3
percentage points in either direction. Specifically, the sample size is
calculated assuming that the universe is ``infinite'' and the error
rate for FFS is 5 percent and the error rate for managed care is 3
percent. (Once the universe contains more than approximately 10,000
sampling units, it can be treated as if it were infinite. Statistically
speaking, beyond a universe of approximately 10,000 sampling units,
universe size does not affect sample size.) Using these assumptions and
historical information on payment variation in FFS and managed care
from previous PERM cycles, we have determined that an annual sample of
500 FFS and 250 managed care payments per State per program should meet
our State-level precision requirements with reasonable probability.
However, States with Medicaid or CHIP PERM universes under 10,000
line items or capitation payments can petition CMS for an annual sample
size smaller than the base sample size in the initial PERM year or
beyond. While the universe can be treated as if it were infinite if its
size exceeds 10,000 sampling units, if the total universe from which
the total (full year) sample is drawn is less than 10,000 sampling
units, the sample size may be reduced by the finite population
correction factor. A State that anticipates that the total number of
payments in the FFS or managed care universe for either Medicaid or
CHIP will be less than 10,000 payments over the Federal fiscal year may
notify CMS before the fiscal year being measured and include
information on the anticipated universe size for their State. Our
contractor will develop a modified sampling plan for that program in
that State.
The State-specific annual sample size in the base PERM year is
based on an assumed error rate of 5 percent. If a State's actual PERM
error rates in a cycle reveals that precision goals can be achieved in
future PERM cycles with either lower or higher sample sizes than
indicated by the original assumptions, sample sizes after the first
PERM cycle may vary among States according to each State's demonstrated
ability, based on PERM experience, to meet desired precision goals.
[[Page 34472]]
In subsequent years, we will provide our contractor with
information on each State's error rate and payment variation in the
previous cycle. Our contractor will review each State's prior PERM
cycle claims error rate and payment variation to determine if a smaller
or larger claims sample size will be required to meet the precision
goal established for that PERM cycle. Our contractor will develop a
State-specific sample size for each program in each State. If
information from a previous cycle is not available for a particular
State or program within the State, the contractor will use the ``base
sample'' size of 500 FFS claims and 250 managed care payments. For
States measured in the FY 2007 or FY 2008 cycle that elect to accept
their State-specific CHIP PERM error rate determined during those
cycles, FY 2007 or FY 2008 would be considered their first PERM cycle
for purposes of sample size calculation for CHIP. Therefore, these
States would be considered for an adjusted sample size in their next
year of measurement after the publication of the new final rule. For
States measured in the FY 2007 or FY 2008 cycle that elect to reject
their State-specific CHIP PERM error rate determined during those
cycles, information from those cycles would not be used to calculate
the State-specific sample sizes and the ``base sample'' size of 500 FFS
claims and 250 managed care payments would be used.
We are proposing to establish a maximum sample size for Medicaid or
CHIP FFS or managed care of 1,000 claims. Additionally, as discussed
above, a State with a claims universe of less than 10,000 sampling
units in a program may notify CMS and the annual sample size will be
reduced by the finite population correction factor for any PERM cycle.
We believe that by taking into consideration prior cycle PERM error
rates, as well as the finite population correction factor in
establishing State-specific sample sizes, the States' administrative
cost burden will be reduced and the program will be manageable at the
State level.
2. Eligibility
The eligibility sampling requirements are described in Sec.
431.978. The universe for the eligibility component is case-based, not
claims-based. The case as a sampling unit only applies to the
eligibility component. For PERM eligibility, the ``universe'' is the
total number of Medicaid or CHIP cases, which, as discussed later in
this proposed rule, is comprised of all beneficiaries, both individuals
and families. The eligibility sampling plan and procedures state that
the total eligibility sample size must be estimated to achieve within a
3 percent precision level at 95 percent confidence interval for the
eligibility component of the program.
For PERM eligibility, the initial sample size is calculated under
the assumption that the error rate is 5 percent and the universe is
greater than 10,000 total cases. This means that the desired precision
requirements will be achieved with a high probability if the actual
error rate is 5 percent or less. For this reason, an annual sample of
504 active cases and 204 negative cases should be selected in a State's
base PERM year to meet State-level precision requirements with a high
probability. Appendix D of the PERM Eligibility Review Instructions
elaborates on the theory of sample size at the State-level for the
dollar-weighted active case error rates, and is on the CMS Web site at
https://www.cms.hhs.gov/perm/downloads/PERM_Eligibility_Review_Guidance.pdf.
Eligibility sampling is performed by the States, and States have
the opportunity to adjust their eligibility sample size based on the
eligibility error rate in the previous PERM cycle. After a State's base
PERM year, we will determine, with input from the State, a sample size
that will meet desired precision goals at lower or higher sample sizes
based on the outcome of the State's previous PERM cycle. The sample
size could either increase or decrease given the results of the
previous year. We are proposing to establish a maximum sample size for
eligibility at 1,000 cases. States must submit an eligibility sampling
plan by August 1st before the fiscal year being measured and include a
proposed sample size for their State. Our contractor will review and
approve all eligibility sampling plans. The State must notify CMS that
it will be using the same plan from the previous review year if the
plan is unchanged. However, we will review State sampling plans from
prior cycles in each PERM cycle to ensure that information is accurate
and up-to-date. States will be asked for revisions when necessary.
As in the claims universe, States with PERM eligibility universes
under 10,000 cases can notify CMS for a reduced eligibility sample size
for either the base year or any subsequent PERM cycle.
Additionally, section 203 of the CHIPRA describes the State option
to enroll children in CHIP based on findings of an express lane agency
that has conducted simplified eligibility determinations. Under section
203(a)(13)(E) of the CHIPRA, an error rate measurement will be created
with respect to the enrollment of children under the express lane
eligibility option. The law directs States not to include children
enrolled using the express lane eligibility option starting April 1,
2009, in data or samples used for purposes of complying with MEQC and
PERM requirements. Provisions for States' express lane option will be
set forth in a future rulemaking document.
We are proposing to revise Sec. 431.814 and Sec. 431.978 to
reflect the changes and clarifications specified above.
B. Error Criteria
Under the PERM program, we identify improper payments through
claims reviews and eligibility reviews. For the claims review, we
perform the following: (1) A data processing review of a sample of FFS
and managed care payments to ensure the payments were processed and
paid in accordance with State and Federal policy; and (2) a medical
review of a sample of FFS payments to ensure that the services were
medically necessary, coded correctly, and provided and documented in
accordance with State and Federal policy. For the eligibility review,
we rely on States to review a sample of beneficiary cases to ensure
that they were eligible for the program and for any services received
and paid for by Medicaid or CHIP (as applicable). The PERM eligibility
review also considers negative cases (cases where eligibility was
denied or terminated). A negative case is in error if the case was
improperly denied or incorrectly terminated. However, because there are
no payments associated with these cases, only a case error rate is
calculated. These errors are not factored into the PERM error rate,
which is a payment error rate.
Under the IPIA, to be considered an improper payment, the error
made must affect payment under applicable Federal policy and State
policy. Improper payments include both overpayments and underpayments.
A payment is also considered improper where it cannot be discerned
whether the payment was proper as a result of insufficient or lack of
documentation.
Consistent with the IPIA, the PERM error rate itself does not
distinguish between ``State'' and ``provider'' errors; all dollars in
error identified through PERM reviews contribute to the State error
rate. In practice, the data processing and eligibility reviews focus on
determinations made by State systems and personnel, while the medical
review focuses on documentation maintained and claims submitted by
providers.
[[Page 34473]]
Section 601(c)(1)(A) of the CHIPRA requires CMS to promulgate a new
final rule that includes clearly defined criteria for errors for both
States and providers. Accordingly, we are proposing to add Sec.
431.960, ``Types of payment errors,'' to clarify that State or provider
errors for purposes of the PERM error rate must affect payment under
applicable Federal policy and State policy, and to generally categorize
data processing errors and eligibility determination errors as State
errors and medical review errors as provider errors. The data
processing errors, medical review errors, and eligibility determination
errors may include, but are not limited to, the types of improper
payments discussed below.
1. Claims Review Error Criteria
a. Data Processing Errors (Generally State Errors)
i. Duplicate Item
The sampled line item/claim is an exact duplicate of another line
item/claim that was previously paid (for example, same patient, same
provider, same date of service, same procedure code, and same
modifier).
ii. Non-Covered Service
The State policy indicates that the service is not payable by
Medicaid or CHIP under the State plan and/or the beneficiary is not in
the coverage category for that service.
iii. Fee-for-Service Claim for a Managed Care Service
The beneficiary is enrolled in a managed care organization that
should have covered the service, but the sampled service was
inappropriately paid by the Medicaid or CHIP FFS component.
iv. Third-Party Liability
The service should have been paid by a third party and was
inappropriately paid by Medicaid or CHIP.
v. Pricing Error
Payment for the service does not correspond with the pricing
schedule on file for the date of service.
vi. Logic Edit
A system edit was not in place based on policy or a system edit was
in place but was not working correctly and the claim line was paid (for
example, incompatibility between gender and procedure).
vii. Data Entry Errors
A claim/line item is in error due to clerical errors in the data
entry of the claim.
viii. Managed Care Rate Cell Error
The beneficiary was enrolled in managed care and payment was made,
but for the wrong rate cell.
ix. Managed Care Payment Error
The beneficiary was enrolled in managed care and assigned to the
correct rate cell, but the amount paid for that rate cell was
incorrect.
x. Other Data Processing Error
Errors not included in any of the above categories.
b. Medical Review Errors (Generally Provider Errors)
i. No Documentation
The provider did not respond to the request for records within the
required timeframe.
ii. Insufficient Documentation
There is not enough documentation to support the service.
iii. Procedure Coding Error
The procedure was performed but billed using an incorrect procedure
code and the result affected the payment amount.
iv. Diagnosis Coding Error
According to the medical record, the diagnosis was incorrect and
resulted in a payment error--as in a Diagnosis Related Group (DRG)
error.
v. Unbundling
The provider separately billed and was paid for the separate
components of a procedure code when only one inclusive procedure code
should have been billed and paid.
vi. Number of Unit(s) Error
The incorrect number of units was billed for a particular
procedure/service, National Drug Code (NDC) units, or revenue code.
vii. Medically Unnecessary Service
The service was medically unnecessary based upon the documentation
of the patient's condition in the medical record.
viii. Policy Violation
A policy is in place regarding the service or procedure performed
and medical review indicates that the service or procedure is not in
agreement with the documented policy.
ix. Administrative/Other Medical Review Error
A payment error was determined by the medical review but does not
fit into one of the other medical review error categories, including
State-specific non-covered services.
c. Eligibility Errors (Generally State Errors)
i. Not Eligible
An individual beneficiary or family is receiving benefits under the
program but does not meet the State's categorical and financial
criteria in the first 30 days of eligibility being verified.
ii. Eligible With Ineligible Services
An individual beneficiary or family meets the State's categorical
and financial criteria for receipt of benefits under the Medicaid or
CHIP program but was not eligible to receive particular services. An
example of ``eligible with ineligible services'' would be a person
eligible under the medically needy group who received services not
provided to the medically needy group.
iii. Undetermined
A beneficiary case subject to a Medicaid or CHIP eligibility
determination review under PERM and which a definitive determination of
eligibility could not be made.
iv. Liability Overstated
The beneficiary paid too much toward his liability amount or cost
of institutional care and the State paid too little.
v. Liability Understated
Beneficiary paid too little toward his liability amount or cost of
institutional care and the State paid too much.
vi. Managed Care Error 1
Ineligible for managed care--Upon verification of residency and
program eligibility, the beneficiary is enrolled in managed care but is
not eligible for managed care.
vii. Managed Care Error 2
Eligible for managed care but improperly enrolled--Beneficiary is
eligible for both the program and for managed care but not enrolled in
the correct managed care plan as of the month eligibility is being
verified.
viii. Improper Denial
The application for program benefits was denied by the State for
not meeting the categorical and/or financial eligibility requirements
but upon review is found to be eligible.
ix. Improper Termination
Based on a completed redetermination, the State determines an
existing beneficiary no longer meets the program's categorical and/or
[[Page 34474]]
financial eligibility requirements and is terminated but upon review is
found to still be eligible.
2. Definitions
Based on the criteria identified in section II.B.1 of this proposed
rule, we are proposing to add the following definitions for ``provider
error'' and ``State error'' to Sec. 431.958.
Provider error includes, but is not limited to, an improper payment
made due to lack of or insufficient documentation, incorrect coding,
improper billing (for example, unbundling, incorrect number of units),
a payment that is in error due to lack of medical necessity, or
evidence that the service was not provided in compliance with
documented State or Federal policy.
State error includes, but is not limited to the following:
A payment that is in error due to incorrect processing
(for example, duplicate of an earlier payment, payment for a non-
covered service, payment for an ineligible beneficiary).
Incorrect payment amount (for example, incorrect fee
schedule or capitation rate applied, incorrect third-party liability
applied).
A payment error resulting from services being provided to
an individual who--
++ Was ineligible when authorized or when he or she received
services;
++ Was eligible for the program but was ineligible for certain
services he or she received; or
++ Had not met applicable beneficiary liability requirements when
authorized eligible or paid too much toward actual liability.
++ Had a lack of sufficient documentation to make a definitive
determination of eligibility or ineligibility.
C. Self-Declaration of Eligibility
Section 601(c)(2) of the CHIPRA requires that the payment error
rate determined for a State shall not take into account payment errors
resulting from the State's verification of an applicant's self-
declaration or self-certification of eligibility for, and the correct
amount of, medical assistance or child health assistance, if the State
process for verifying an applicant's self-declaration or self-
certification satisfies the requirements for such process applicable
under regulations promulgated by the Secretary or otherwise approved by
the Secretary.
Accordingly, we are proposing to specify in the new Sec. 431.960
that the dollars paid in error due to the eligibility error is the
measure of the payment error. A State eligibility error does not result
from the State's verification of an applicant's self-declaration or
self-certification of eligibility for, and the correct amount of,
medical assistance or child health assistance, if the State process for
verifying an applicant's self-declaration or self-certification
satisfies the requirements for such process applicable under
regulations at Sec. 457.380 of this chapter, in CMS approved State
Plans, or otherwise approved by the Secretary.
We also propose to modify Sec. 431.980 to provide review
requirements for acceptable self-declaration. We would also modify the
PERM eligibility instructions, found at https://www.cms.hhs.gov/perm/downloads/PERM_Eligibility_Review_Guidance.pdf. These instructions,
which clarify and provide additional guidance in implementing the
regulations, reflect the new review procedures for self declaration.
Currently, States are required to review the case record and
independently verify elements of eligibility where evidence is missing,
or outdated and likely to change, or otherwise as needed. The
instructions and the regulation would provide that ``a self-declaration
statement for Medicaid or CHIP is acceptable verification for the PERM
reviews for elements of eligibility in which State policy allows for
self-declaration. A self-declaration statement must be--
Present in the record;
Not outdated (more than 12 months old);
In a valid, State approved format; and
Consistent with other facts in the case record.
A State may verify eligibility through a new self-declaration
statement, depending on State policies on self-declaration. We propose
that if a new self-declaration statement cannot be obtained for the
PERM review, the State may verify eligibility using third party
sources, for example, documentation listed in section 7269 of the State
Medicaid Manual. Verifying a self-declaration statement with third
party verification when a beneficiary does not provide a new self-
declaration statement is the only new review procedure being added.
After all minimum efforts listed in the eligibility instructions have
been exhausted, a case should be cited as Undetermined if sufficient
documentation cannot be obtained to complete the eligibility review. We
are proposing that these Undetermined cases would not be included in
the State-specific payment error rate. However, we are proposing to
specify in the new Sec. 431.960 that these errors be tracked
nationally by including these Undetermined cases in the national
program payment error rates.
D. Difference Resolution and Appeals Process
Section 601(c)(1)(B) of the CHIPRA requires CMS to include in the
new final rule for PERM a clearly defined process for appealing error
determinations by review contractors or State agency and personnel
responsible for the development, direction, implementation, and
evaluation of eligibility reviews and associated activities.
1. Medical and Data Processing Review
The October 5, 2005 IFC established the difference resolution
process, which is codified at Sec. 431.998. Medical reviews and data
processing reviews for FFS and managed care payments are conducted by
an independent Federal contractor. States supply relevant policies but
do not participate in the review; States are notified of all error
findings. The difference resolution process is the mechanism by which a
State may try to resolve with the Federal contractor differences in the
Federal contractor's error findings; the State may appeal to CMS if it
cannot resolve the difference in findings with the Federal contractor.
In accordance with the CHIPRA, we are providing more detail in this
proposed rule by proposing the timeline associated with the difference
resolution and CMS appeals processes. We are also revising the heading
of Sec. 431.998 to read, ``Difference resolution and appeal process,''
which more accurately describes the regulation.
We are proposing to revise Sec. 431.998 to explain that the State
may file, in writing, a request with the Federal contractor to resolve
differences in the Federal contractor's findings based on medical or
data processing reviews of FFS and managed care claims in Medicaid or
CHIP within 10 business days after the disposition report of claims
review findings is posted on the contractor's Web site. Additionally,
the State may appeal to CMS for a final resolution within 5 business
days from the date the contractor's finding as a result of the
difference resolution is posted on its Web site.
In addition to establishing the timeline for the difference
resolution and appeal processes, we are proposing to eliminate the
dollar threshold for engaging in the CMS appeals process. Section
431.998 currently provides that States may apply to the Federal
contractor to resolve differences in
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findings and may appeal to CMS for final resolution for any claims in
which the State and Federal contractor cannot resolve the difference in
findings, as long as the difference in findings is in the amount of
$100 or more. We established the $100 threshold in order to prevent de
minimis disputes and to ensure that appeals to CMS were substantial
enough to warrant reconsideration. We were also concerned that a large
volume of small-dollar appeals would prevent the States from receiving
timely decisions on their appeals.
Information from the FY 2006 and FY 2007 PERM cycles on the number
of total claims (including those with errors less than $100) submitted
to the Federal contractor for difference resolution and on the number
appealed to CMS for final resolution suggests that the volume of
appeals will not substantially increase if CMS allows appeals of errors
of less than $100. Because all errors regardless of their dollar amount
ultimately contribute to a State's error rate and hence the national
error rate, we are proposing to remove the $100 threshold set forth in
Sec. 431.998(b)(1).
2. Eligibility
As stated in the current PERM regulations at Sec. 431.974(a)(2),
personnel responsible for PERM eligibility sampling and review ``must
be functionally and physically separate from the State agencies and
personnel that are responsible for Medicaid and CHIP policy and
operations, including eligibility determinations.'' The intent of this
provision was to ensure the independence of the review in order to
achieve an unbiased error rate. We provided further clarification in
the preamble of the August 2007 final rule, indicating that the agency
responsible for PERM could be under the same umbrella agency that
oversees policy, operations and determinations but the two agencies
cannot report to the same supervisor.
We would further clarify that qualified staff with knowledge of
State eligibility policies may be used to conduct the eligibility
reviews, but the staff that is chosen must be independent from the
staff that oversees policy and operations. Further, the PERM
eligibility instructions ask States to provide assurance that the
agency or contracting entity responsible for the eligibility reviews is
independent of the State agency responsible for eligibility
determination and enrollment. The State is responsible for ensuring the
integrity of the eligibility reviews, but we do not preclude the
independent State agency from sharing or reporting the eligibility
findings to other agencies or stakeholders.
Provided that agency independence could cause a difference in
findings between the independent agency and other stakeholder agencies
at the State level, we propose that appeals for eligibility review
findings should be conducted in accordance with the State's appeal
process, as eligibility reviews are conducted at the State level.
In consideration of States that may not have a State appeals
process in place, we are also proposing to make State findings
available to each respective State's stakeholders (that is, the State
Medicaid or CHIP agency), with certain limitations, for the period
between the final monthly payment findings submission and eligibility
error rate calculation, for example, April 15th through June 15th after
the fiscal year being measured or according to the eligibility
timeline. We propose facilitating documentation exchange between the
State Medicaid or CHIP agency and the independent State agency
conducting the PERM eligibility reviews to resolve differences. If any
eligibility appeals issues involve Federal policy, States can appeal to
CMS for resolution. If our decision causes an erroneous payment finding
to be made, any resulting recoveries will be governed by Sec.
431.1002.
Other stakeholder agencies may document their differences in
writing to the independent State agency for consideration. If
resolutions of differences occur during the PERM cycle, eligibility
findings can be updated to reflect the resolution. If differences are
not resolved by the deadline for eligibility findings to be submitted
to CMS (July 1), the documentation of the difference can be submitted
to CMS for consideration no sooner than 60 days and no later than 90
days after the deadline for eligibility findings.
We are also seeking comment on other ways that we can implement an
eligibility appeals process for which we can provide consistent
oversight.
E. Harmonization of Medicaid Eligibility Quality Control (MEQC) and
PERM Programs
1. Options for Applying PERM and MEQC Data
Section 601(e)(2) of the CHIPRA requires that, once this final rule
is effective for all States, States will be given the option to elect,
for purposes of determining the erroneous excess payments for medical
assistance ratio applicable to the State for a fiscal year under
section 1903(u) of the Act, to substitute data resulting from the
application of the PERM requirements to the State for data obtained
from the application of the MEQC requirements to the State with respect
to a fiscal year. Because under section 601(b) of the CHIPRA, there
shall be no calculation or publication of any national or State-
specific CHIP error rates until 6 months after the final rule becomes
effective, States will not have the option to substitute PERM data for
MEQC data until 6 months after this final rule is effective.
We considered several interpretations of the CHIPRA requirements
that would allow States the option to substitute MEQC data for PERM
data and vice versa for purposes of the PERM Medicaid eligibility
reviews, but would also retain two separate, independent processes
(MEQC and PERM), which are governed by separate statutes and
regulations. As PERM is required to meet specific statistical precision
requirements and the MEQC error rate is not, we do not believe it is
feasible to incorporate the MEQC error rate into a State's overall PERM
error rate. Therefore, we interpret ``data'' as the sample, eligibility
review findings, and payment findings as measured under MEQC or PERM.
We will calculate separate rates for each program. We are proposing to
amend Sec. 431.806 and Sec. 431.812 of the MEQC regulations. These
proposed amendments would provide for the State's option in its PERM
year to use their samples, eligibility findings and payment findings as
measured using PERM sampling and review requirements to meet their MEQC
review requirement. States operating under MEQC waivers and pilot
programs cannot use this option. Therefore, to provide requirements for
implementing a pilot or waiver MEQC program, we are proposing revisions
to the MEQC regulation at Sec. 431.812. We are proposing that States
that choose to substitute PERM data for MEQC data, would still have two
eligibility error rates calculated -- one for MEQC using MEQC
measurement requirements and one for PERM using PERM requirements. We
are proposing to revise Sec. 431.806 of the MEQC regulations to
require that a State plan provide a State plan amendment for States
opting to use PERM for MEQC in a State's PERM cycle.
We are proposing to amend Sec. 431.812 of the MEQC regulation to
provide that States substituting PERM data for MEQC data must use a
sampling plan that meets the requirements of Sec. 431.978 of the PERM
regulation and perform active
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case reviews in accordance with Sec. 431.980 of the PERM regulation.
We are proposing that States with CHIP stand alone programs will
only have the option to substitute PERM Medicaid data to meet MEQC
requirements under Sec. 431.812(a) through (e) since CHIP stand alone
programs are not reviewed under MEQC.
We are also proposing that States with Medicaid and Title XXI
Medicaid expansion programs may use Medicaid and CHIP PERM reviews to
meet the MEQC requirements described under Sec. 431.812(a) through
(e), as both Medicaid and Title XXI Medicaid expansion programs are
reviewed under MEQC. States with Title XXI Medicaid expansion programs
must combine their Medicaid and CHIP PERM findings to calculate one
MEQC error rate. The data must be kept separate for purposes of
calculating the PERM error rate.
In addition, we are proposing that States with combination CHIP
programs, in which a portion of their CHIP cases are under a stand
alone program and a portion of their CHIP cases are under a Title XXI
Medicaid expansion program, may use the PERM Medicaid eligibility
reviews and the portion of the PERM CHIP eligibility reviews under
Title XXI Medicaid expansion programs to meet their MEQC requirement.
The Federal contractor will combine the CHIP case findings under the
Title XXI Medicaid expansion program and CHIP stand alone findings to
calculate one PERM CHIP error rate. The Title XXI Medicaid expansion
portion of the PERM data must be included with the Medicaid PERM data
to calculate the MEQC error rate.
Section 601(e)(3) of the CHIPRA provides that for purposes of
satisfying the requirements of the PERM regulation relating to Medicaid
eligibility reviews, a State may elect to substitute data obtained
through MEQC reviews conducted in accordance with section 1903(u) of
the Act for data required for purposes of PERM requirements, but only
if the State MEQC reviews are based on a broad, representative sample
of Medicaid applicants or enrollees in the States. The CHIPRA's general
effective date of April 1, 2009 applies to this provision. Therefore,
as of April 1, 2009, States have the option to substitute MEQC data for
PERM data so long as the MEQC reviews are based on a broad,
representative sample of Medicaid applicants or enrollees in the
States.
We interpret ``broad, representative sample of Medicaid applicants
or enrollees'' to mean that States must develop the MEQC universe
according to requirements at Sec. 431.814 in order to consider the
option to use one program's findings to meet the requirements for the
other. Under Sec. 431.814, States must sample from a universe of all
Medicaid and Title XXI Medicaid expansion beneficiaries (except for the
exclusions provided in Sec. 431.814(c)(4)). States operating MEQC
pilots or waivers will need to continue operating PERM separately from
MEQC.
We are proposing that States with CHIP stand alone programs only
have the option to substitute Medicaid MEQC data to meet the PERM
Medicaid eligibility review requirement, as CHIP stand alone is not
reviewed under the MEQC review.
We are also proposing that States with Title XXI Medicaid expansion
programs may use their MEQC reviews described in Sec. 431.812(a)
through (e) to meet both the PERM Medicaid and CHIP eligibility review
requirements, as both Medicaid and Title XXI Medicaid expansion are
reviewed under MEQC. Title XXI Medicaid expansion data must be
separated from the MEQC Medicaid data to calculate a PERM CHIP error
rate.
We are also proposing that States with combination programs in
which a portion of their CHIP cases are under a stand alone program and
a portion of their CHIP cases are under a Title XXI Medicaid expansion
program may use the MEQC reviews described under Sec. 431.812 (a)
through (e) to meet the PERM Medicaid eligibility review requirement
and the portion of the PERM CHIP eligibility review requirement under
Title XXI Medicaid expansion. However, the stand alone portion of the
CHIP universe must remain separate and stratified, as defined in Sec.
431.978(d)(3), as CHIP stand alone is not a part of the harmonization
of PERM and MEQC. The Federal contractor, who we are proposing will
calculate State eligibility error rates, will combine the Title XXI
Medicaid expansion and CHIP stand alone findings to calculate one PERM
CHIP error rate.
In addition, we are proposing to amend Sec. 431.980 to allow for
States in their PERM year the option to use their MEQC samples,
eligibility findings, and payment findings to meet their PERM
eligibility review requirement. MEQC reporting requirements to the CMS
Regional Offices remain the same, including reporting the error
findings for the two 6-month review periods, but States will also be
required to comply with the PERM eligibility reporting deadlines by
posting error findings to the PERM Error Rate Tracking (PERT) Web site
or other electronic eligibility findings repository specified by CMS.
We are proposing that States that choose to substitute MEQC data for
PERM data, will still have two eligibility error rates calculated--one
for MEQC using MEQC measurement requirements and one for PERM using
PERM requirements.
States that choose to substitute MEQC data must ensure that the
Medicaid and Title XXI Medicaid expansion sample sizes meet PERM
precision requirements when they are separated. States must also note
that if using MEQC data, any cases sampled under Sec. 431.814(c)(4)
must be excluded from the PERM sample. For example, State-only funded
cases, should be reported separately.
States that choose to substitute MEQC or PERM data should note that
although two error rates are calculated, only the MEQC error rate will
be subject to disallowances under section 1903(u) of the Act. PERM does
not have a threshold for eligibility errors and any improper payments
identified during the eligibility measurement are subject to recovery
according to Sec. 431.1002 of the regulations.
If a State chooses to substitute PERM or MEQC data, the State may
not dispute error findings or the eligibility error rate based on the
possibility that findings would not have been in error had the other
review methodology been used.
We are also seeking comments on the following alternative process
for the substitution of MEQC and PERM data: States would select one
annual sample that meets MEQC minimum sample requirements and PERM
confidence and precision requirements. The State would conduct both an
MEQC review and a PERM review on each applicable case. This would
ensure a clear distinction between an MEQC error and a PERM eligibility
error, and will be the basis for the MEQC error rate and the PERM
eligibility error rate