Agency Information Collection Activities: Proposed Collection; Comment Request, 20643-20646 [2016-08106]
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Federal Register / Vol. 81, No. 68 / Friday, April 8, 2016 / Notices
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that increase the probability of a patient
safety event.
AHRQ’s Common Formats for patient
safety event reporting include:
• Event descriptions (definitions of
patient safety events, near misses, and
unsafe conditions to be reported);
• Specifications for patient safety
aggregate reports and individual event
summaries that derive from event
descriptions;
• Delineation of data elements and
algorithms to be used for collection of
adverse event data to populate the
reports; and
• Technical specifications for
electronic data collection and reporting.
The technical specifications promote
standardization of collected patient
safety event information by specifying
rules for data collection and submission,
as well as by providing guidance for
how and when to create data elements,
their valid values, conditional and go-to
logic, and reports. These specifications
will ensure that data collected by PSOs
and other entities have comparable
clinical meaning. They also provide
direction to software developers, so that
the formats can be implemented
electronically, and to PSOs, so that the
Common Formats can be submitted
electronically to the PSO Privacy
Protection Center (PSOPPC) for data deidentification and transmission to the
Network of Patient Safety Databases
(NPSD).
Common Formats Development
In anticipation of the need for
Common Formats, AHRQ began their
development by creating an inventory of
functioning private and public sector
patient safety reporting systems. This
inventory provided an evidence base to
inform construction of the Common
Formats. The inventory included many
systems from the private sector,
including prominent academic settings,
hospital systems, and international
reporting systems (e.g., from the United
Kingdom and the Commonwealth of
Australia). In addition, virtually all
major Federal patient safety reporting
systems were included, such as those
from the Centers for Disease Control and
Prevention (CDC), the Food and Drug
Administration (FDA), the Department
of Defense (DoD), and the Department of
Veterans Affairs (VA).
Since February 2005, AHRQ has
convened the PSWG to assist AHRQ
with developing and maintaining the
Common Formats. The PSWG includes
major health agencies within HHS—
CDC, Centers for Medicare & Medicaid
Services, FDA, Health Resources and
Services Administration, Indian Health
Service, National Institutes of Health,
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National Library of Medicine, Office of
the National Coordinator for Health
Information Technology, Office of
Public Health and Science, and
Substance Abuse and Mental Health
Services Administration—as well as the
DoD and VA.
When developing Common Formats,
AHRQ first reviews existing patient
safety practices and event reporting
systems. In collaboration with the
PSWG and Federal subject matter
experts, AHRQ drafts and releases beta
versions and updates to current versions
of the Common Formats for public
review and comment. The prior version
of Common Formats for Event Reporting
for Hospitals, Version 1.2, was released
in April 2013. The PSWG assists AHRQ
with assuring the consistency of
definitions/formats with those of
relevant government agencies as
refinement of the Common Formats
continues.
Since the initial release of the
Common Formats in August 2008,
AHRQ has regularly revised the formats
based upon public comment. AHRQ
solicits feedback on beta, and
subsequent, versions of Common
Formats from private sector
organizations and individuals. Based
upon the feedback received, AHRQ
further revises the formats. To the extent
practicable, the Common Formats are
also aligned with World Health
Organization (WHO) concepts,
frameworks, and definitions.
Participation by the private sector in
the development and subsequent
revision of the Common Formats is
achieved through working with the
NQF. The Agency engages the NQF, a
non-profit organization focused on
health care quality, to solicit comments
and advice regarding proposed versions
of the Common Formats. AHRQ began
this process with the NQF in 2008,
receiving feedback on AHRQ’s 0.1 Beta
release of the Common Formats for
Event Reporting—Hospital. After
receiving public comment, the NQF
solicits the review and advice of its
Common Formats Expert Panel and
subsequently provides feedback to
AHRQ. The Agency then revises and
refines the Common Formats and issues
them as a production version. AHRQ
has continued to employ this process for
all subsequent versions of the formats.
Commenting on Common Formats for
Event Reporting—Hospital Version 2.0
AHRQ used a tiered approach to
develop Hospital Version 2.0. This
approach was done in response to
feedback from PSOs and the public to
decrease the number of questions for
each module of the formats in order to
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20643
reduce the burden on health care
providers and to facilitate data
transmission. These formats have two
tiers, or data sets. The first tier, or
national data set, contains elements that
are collected for submission to the
PSOPPC. The second tier, or local data
set, is optional and is designed for use
at the local level for additional analyses.
This local data set is not meant for
transmission to the PSOPPC.
The Agency is specifically interested
in obtaining feedback from both the
private and public sectors on the
updated Common Formats for Event
Reporting—Hospitals Version 2.0. At
this time, only the event descriptions—
which define adverse events of interest
in the inpatient hospital setting—are
available. Other elements of the
Common Formats, including aggregate
reports and technical specifications,
will be developed following revision of
the Common Formats for Hospital
Version 2.0 based on public comment
and NQF advice. Information on how to
comment and provide feedback on the
Common Formats for Hospital Version
2.0 is available at the NQF Web site:
https://www.qualityforum.org/Project_
Pages/Common_Formats_for_Patient_
Safety_Data.aspx.
AHRQ appreciates the time and effort
individuals invest in providing
comments. The Agency will review and
consider all feedback received to help
guide the development of a revised
version. The process for updating and
refining the formats will continue to be
an iterative one.
Further information on the Common
Formats can be obtained through
AHRQ’s PSO Web site: https://
www.pso.ahrq.gov/. To receive
notifications about final versions of
AHRQ Common Formats, please
subscribe to ‘‘E-Mail Updates’’ at:
https://pso.ahrq.gov/about/subscribe.
Sharon B. Arnold,
Acting Director.
[FR Doc. 2016–08021 Filed 4–7–16; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–317, CMS–319,
CMS–10166, CMS–10178, and CMS–10184]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services.
AGENCY:
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ACTION:
Federal Register / Vol. 81, No. 68 / Friday, April 8, 2016 / Notices
Notice.
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
SUMMARY:
Comments must be received by
June 7, 2016.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number ___, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/Paperwork
ReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
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DATES:
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3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–317 State Medicaid Eligibility
Quality Control Sampling Plan
CMS–319 State Medicaid Eligibility
Quality Control Sample Selection
Lists
CMS–10166 Payment Error Rate
Measurement in Medicaid and the
State Children’s Health Insurance
Program
CMS–10178 Medicaid and State
Children’s Health Insurance Plan
(SCHIP) Managed Care
CMS–10184 Payment Error Rate
Measurement—State Medicaid and
SCHIP Eligibility
Under the PRA (44 U.S.C. 3501–
3520), federal agencies must obtain
approval from the Office of Management
and Budget (OMB) for each collection of
information they conduct or sponsor.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: State Medicaid
Eligibility Quality Control (MEQC)
Sample Plans; Use: The Medicaid
Eligibility Quality Control (MEQC)
system is based on monthly State
reviews of Medicaid and Medicaid
expansion under Title XXI cases by
States performing the traditional
sampling process identified through
statistically reliable statewide samples
of cases selected from the eligibility
files. These reviews are conducted to
determine whether or not the sampled
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cases meet applicable State Title XIX or
XXI eligibility requirements when
applicable. The reviews are also used to
assess beneficiary liability, if any, and to
determine the amounts paid to provide
Medicaid services for these cases. In the
MEQC system, sampling is the only
practical method of validating eligibility
of the total caseload and determining
the dollar value of eligibility liability
errors. Any attempt to make such
validations and determinations by
reviewing every case would be an
enormous and unwieldy undertaking. In
1993, CMS implemented MEQC pilots
in which States could focus on special
studies, targeted populations,
geographic areas or other forms of
oversight with CMS approval. States
must submit a sampling plan, or pilot
proposal to be approved by CMS before
implementing their pilot program. The
Children’s Health Insurance Program
Reauthorization Act (CHIPRA) was
enacted February 4, 2009. Sections 203
and 601 of the CHIPRA relate to MEQC.
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 requirements. Section 601 of the
CHIPRA, among other things, requires a
new final rule for the Payment Error
Rate Measurement (PERM) program and
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. We review,
either directly or through its contractors,
of the sampling plans helps to ensure
States are using valid statistical methods
for sample selection. The collection of
information is also necessary to
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. Form
Number: CMS–317 (OMB control
number: 0938–0146); Frequency: SemiAnnually Affected Public: State, Local,
or Tribal Governments; Number of
Respondents: 10; Total Annual
Responses: 20; Total Annual Hours:
480. (For policy questions regarding this
collection contact Bridgett Rider at 410–
786–2602.)
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
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Federal Register / Vol. 81, No. 68 / Friday, April 8, 2016 / Notices
Information Collection: State Medicaid
Eligibility Quality Control (MEQC)
Sample Selection Lists; Use: The MEQC
system is based on monthly State
reviews of Medicaid and Medicaid
expansion under Title XXI cases by
States performing the traditional
sampling process identified through
statistically reliable statewide samples
of cases selected from the eligibility
files. These reviews are conducted to
determine whether or not the sampled
cases meet applicable State Title XIX or
XXI eligibility requirements when
applicable. The reviews are also used to
assess beneficiary liability, if any, and to
determine the amounts paid to provide
Medicaid services for these cases. In the
MEQC system, sampling is the only
practical method of validating eligibility
of the total caseload and determining
the dollar value of eligibility liability
errors. Any attempt to make such
validations and determinations by
reviewing every case would be an
enormous and unwieldy undertaking.
At the beginning of each month, State
agencies still performing the traditional
sample are required to submit sample
selection lists which identify all of the
cases selected for review in the States’
samples. The sample selection lists
contain identifying information on
Medicaid beneficiaries such as: State
agency review number, beneficiary’s
name and address, the name of the
county where the beneficiary resides,
Medicaid case number, etc. The
submittal of the sample selection lists is
necessary for Regional Office validation
of State reviews. Without these lists, the
integrity of the sampling results would
be suspect and the Regional Offices
would have no data on the adequacy of
the States’ monthly sample draw or
review completion status. The authority
for collecting this information is Section
1903(u) of the Social Security Act. The
specific requirement for submitting
sample selection lists is described in
regulations at 42 CFR 431.814(h).
Regional Office staff review the sample
selection lists to determine that States
are sampling a sufficient number of
cases for review. Form Number: CMS–
319 (OMB control number: 0938–0147);
Frequency: Monthly; Affected Public:
State, Local, or Tribal Governments;
Number of Respondents: 10; Total
Annual Responses: 120; Total Annual
Hours: 960. (For policy questions
regarding this collection contact
Bridgett Rider at 410–786–2602.)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Payment Error
Rate Measurement in Medicaid &
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Children’s Health Insurance Program
(CHIP); Use: The Improper Payments
Information Act (IPIA) of 2002 as
amended by the Improper Payments
Elimination and Recovery Improvement
Act (IPERIA) of 2012 requires CMS to
produce national error rates for
Medicaid and Children’s Health
Insurance Program (CHIP). To comply
with the IPIA, CMS will engage a
Federal contractor to produce the error
rates in Medicaid and CHIP. The error
rates for Medicaid and CHIP are
calculated based on the reviews on three
components of both Medicaid and CHIP
program. They are: Fee-for-service
claims medical reviews and data
processing reviews, managed care
claims data-processing reviews, and
eligibility reviews. Each of the review
components collects different types of
information, and the state-specific error
rates for each of the review components
will be used to calculate an overall
state-specific error rate, and the
individual state-specific error rates will
be used to produce a national error rate
for Medicaid and CHIP. The states will
be requested to submit, at their option,
test data which include full claims
details to the contractor prior to the
quarterly submissions to detect
potential problems in the dataset to and
ensure the quality of the data. These
states will be required to submit
quarterly claims data to the contractor
who will pull a statistically valid
random sample, each quarter, by strata,
so that medical and data processing
reviews can be performed. State-specific
error rates will be based on these review
results. We need to collect the fee-forservice claims data, medical policies,
and other information from states as
well as medical records from providers
in order for the contractor to sample and
review adjudicated claims in those
states selected for medical reviews and
data processing reviews. Based on the
reviews, state-specific error rates will be
calculated which will serve as part of
the basis for calculating national
Medicaid and CHIP error rates. Form
Number: CMS–10166 (OMB control
number: 0938–0974); Frequency:
Annually, Quarterly; Affected Public:
State, Local, or Tribal Governments;
Number of Respondents: 34; Total
Annual Responses: 34; Total Annual
Hours: 56,100. (For policy questions
regarding this collection contact
Bridgett Rider at 410–786–2602.)
4. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Medicaid and
Children’s Health Insurance (CHIP)
Managed Care Claims and Related
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20645
Information; Use: The Payment Error
Rate Measurement (PERM) program
measures improper payments for
Medicaid and the State Children’s
Health Insurance Program (SCHIP). The
program was designed to comply with
the Improper Payments Information Act
(IPIA) of 2002 and the Office of
Management and Budget (OMB)
guidance. Although OMB guidance
requires error rate measurement for
SCHIP, 2009 SCHIP legislation
temporarily suspended PERM
measurement for this program and
changed to Children’s Health Insurance
Program (CHIP) effective April 01, 2009.
See Children’s Health Insurance
Program Reauthorization Act of 2009
(CHIPRA) Public Law 111–3 for more
details. There are two phases of the
PERM program, the measurement phase
and the corrective action phase. The
PERM measures improper payments in
Medicaid and CHIP and produces State
and national-level error rates for each
program. The error rates are based on
reviews of Medicaid and CHIP fee-forservice (FFS) and managed care
payments made in the Federal fiscal
year under review. States conduct
eligibility reviews and report eligibility
related payment error rates also used in
the national error rate calculation. We
created a 17 State rotation cycle so that
each State will participate in PERM
once every three years. Following is the
list of States in which we will measure
improper payments over the next three
years in Medicaid. We need to collect
capitation payment information from
the selected States so that the federal
contractor can draw a sample and
review the managed care capitation
payments. We will also collect State
managed care contracts, rate schedules
and updates to the contracts and rate
schedules. This information will be
used by the Federal contractor when
conducting the managed care claims
reviews. Sections 1902(a)(6) and
2107(b)(1) of the Social Security Act
grants CMS authority to collect
information from the States. The IPIA
requires us to produce national error
rates in Medicaid and CHIP fee-forservice, including the managed care
component. The State-specific Medicaid
managed care and CHIP managed care
error rates will be based on reviews of
managed care capitation payments in
each program and will be used to
produce national Medicaid managed
care and CHIP managed care error rates.
Form Number: CMS–10178 (OMB
control number: 0938–0994); Frequency:
Occasionally; Affected Public: State,
Local, or Tribal Governments; Number
of Respondents: 34; Total Annual
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Federal Register / Vol. 81, No. 68 / Friday, April 8, 2016 / Notices
Responses: 28,050; Total Annual Hours:
28,050. (For policy questions regarding
this collection contact Bridgett Rider at
410–786–2602.)
5. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Eligibility Error
Rate Measurement in Medicaid and the
Children’s Health Insurance Program;
Use: The Improper Payments
Information Act (IPIA) of 2002 requires
CMS to produce national error rates for
Medicaid and the Children’s Health
Insurance Program (CHIP). To comply
with the IPIA, CMS will use a national
contracting strategy to produce error
rates for Medicaid and CHIP fee-forservice and managed care improper
payments. The federal contractor will
review States on a rotational basis so
that each State will be measured for
improper payments, in each program,
once and only once every three years.
Subsequent to the first publication, we
determined that we will measure
Medicaid and CHIP in the same State.
Therefore, States will measure Medicaid
and CHIP eligibility in the same year
measured for fee-for-service and
managed care. We believe this approach
will advantage States through
economies of scale (e.g. administrative
ease and shared staffing for both
programs reviews). We also determined
that interim case completion timeframes
and reporting are critical to the integrity
of the reviews and to keep the reviews
on schedule to produce a timely error
rate. Lastly, the sample sizes were
increased slightly in order to produce an
equal sample size per strata each month.
Periodically, CMS will conduct Federal
re-reviews of States’ PERM files to
ensure the accuracy of States’ review
findings and the validity of the review
process. CMS will select a random
subsample of Medicaid and CHIP cases
from the sample selection lists provided
by each State. States will submit all
pertinent information related to the
review of each sampled case that is
selected by CMS. Form Number: CMS–
10184 (OMB control number: 0938–
1012); Frequency: Annually, Quarterly
Affected Public: State, Local, or Tribal
Governments; Number of Respondents:
34; Total Annual Responses: 1,583;
Total Annual Hours: 946,164. (For
policy questions regarding this
collection contact Bridgett Rider at 410–
786–2602.)
Dated: April 5, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–08106 Filed 4–7–16; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: National Survey of Child and
Adolescent Well-Being-Third Cohort
(NSCAW III): Agency Recruitment.
OMB No.: 0970–0202.
Description: The Administration for
Children and Families (ACF) within the
U.S. Department of Health and Human
Services (HHS) intends to collect data
on a third cohort of children and
families for the National Survey of Child
and Adolescent Well-Being (NSCAW).
NSCAW is the only source of nationally
representative, longitudinal, firsthand
information about the functioning and
well-being, service needs, and service
utilization of children and families who
come to the attention of the child
welfare system. The first two cohorts of
NSCAW were collected beginning in
1999 and 2008 and studied children
who had been the subject of
investigation by Child Protective
Services. Children were sampled from
child welfare agencies nationwide. The
proposed data collection plan for the
third cohort of NSCAW includes two
phases: Phase 1 includes child welfare
agency recruitment and collection of
files for sampling children, and Phase 2
includes baseline data collection and an
18-month follow-up data collection. The
current data collection plan calls for
selecting a new cohort of 4,565 children
and families and repeating similar data
collection procedures as the previous
two cohorts. This Notice is specific to
Phase 1. The overall goal is to recruit
child welfare agencies in 83 primary
sampling units nationwide. Child
welfare agencies will be selected with
probability proportional to size, based
on the current distributions in the child
welfare system. Child welfare agency
recruitment will include: mail, email,
phone calls, and site visits with child
welfare agency administrators.
Respondents: Child welfare agency
administrators and other personnel.
Data collection will take place over a 2year period.
ANNUAL BURDEN ESTIMATES
Total number
of respondents
Instrument
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Information package for agency administrators ..................
Initial visit or call with agency staff ......................................
Visit or call with agency staff explaining the sample file
process .............................................................................
Agency staff monthly sample file generation and transmission .............................................................................
Estimated Total Annual Burden
Hours: 767.
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
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Annual
number of
respondents
(rounded)
Frm 00041
Average
burden hours
per response
Annual burden
hours
83
83
42
42
1
1
.25
1
11
42
83
42
1
2
84
83
42
15
1
630
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 330 C Street SW.,
Washington, DC 20201, Attn: OPRE
Reports Clearance Officer. Email
address: OPREinfocollection@
acf.hhs.gov. All requests should be
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responses per
respondent
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identified by the title of the information
collection.
The Department specifically requests
comments on (a) whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
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Agencies
[Federal Register Volume 81, Number 68 (Friday, April 8, 2016)]
[Notices]
[Pages 20643-20646]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-08106]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-317, CMS-319, CMS-10166, CMS-10178, and CMS-
10184]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services.
[[Page 20644]]
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (the PRA), federal agencies are required to publish notice
in the Federal Register concerning each proposed collection of
information (including each proposed extension or reinstatement of an
existing collection of information) and to allow 60 days for public
comment on the proposed action. Interested persons are invited to send
comments regarding our burden estimates or any other aspect of this
collection of information, including any of the following subjects: (1)
The necessity and utility of the proposed information collection for
the proper performance of the agency's functions; (2) the accuracy of
the estimated burden; (3) ways to enhance the quality, utility, and
clarity of the information to be collected; and (4) the use of
automated collection techniques or other forms of information
technology to minimize the information collection burden.
DATES: Comments must be received by June 7, 2016.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number. To be assured consideration, comments and
recommendations must be submitted in any one of the following ways:
1. Electronically. You may send your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) that are accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number ___, Room C4-26-05, 7500 Security Boulevard, Baltimore,
Maryland 21244-1850.
To obtain copies of a supporting statement and any related forms
for the proposed collection(s) summarized in this notice, you may make
your request using one of following:
1. Access CMS' Web site address at https://www.cms.hhs.gov/PaperworkReductionActof1995.
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at (410) 786-1326.
FOR FURTHER INFORMATION CONTACT: Reports Clearance Office at (410) 786-
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the use and burden associated
with the following information collections. More detailed information
can be found in each collection's supporting statement and associated
materials (see ADDRESSES).
CMS-317 State Medicaid Eligibility Quality Control Sampling Plan
CMS-319 State Medicaid Eligibility Quality Control Sample Selection
Lists
CMS-10166 Payment Error Rate Measurement in Medicaid and the State
Children's Health Insurance Program
CMS-10178 Medicaid and State Children's Health Insurance Plan (SCHIP)
Managed Care
CMS-10184 Payment Error Rate Measurement--State Medicaid and SCHIP
Eligibility
Under the PRA (44 U.S.C. 3501-3520), federal agencies must obtain
approval from the Office of Management and Budget (OMB) for each
collection of information they conduct or sponsor. The term
``collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA requires federal agencies
to publish a 60-day notice in the Federal Register concerning each
proposed collection of information, including each proposed extension
or reinstatement of an existing collection of information, before
submitting the collection to OMB for approval. To comply with this
requirement, CMS is publishing this notice.
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: State Medicaid
Eligibility Quality Control (MEQC) Sample Plans; Use: The Medicaid
Eligibility Quality Control (MEQC) system is based on monthly State
reviews of Medicaid and Medicaid expansion under Title XXI cases by
States performing the traditional sampling process identified through
statistically reliable statewide samples of cases selected from the
eligibility files. These reviews are conducted to determine whether or
not the sampled cases meet applicable State Title XIX or XXI
eligibility requirements when applicable. The reviews are also used to
assess beneficiary liability, if any, and to determine the amounts paid
to provide Medicaid services for these cases. In the MEQC system,
sampling is the only practical method of validating eligibility of the
total caseload and determining the dollar value of eligibility
liability errors. Any attempt to make such validations and
determinations by reviewing every case would be an enormous and
unwieldy undertaking. In 1993, CMS implemented MEQC pilots in which
States could focus on special studies, targeted populations, geographic
areas or other forms of oversight with CMS approval. States must submit
a sampling plan, or pilot proposal to be approved by CMS before
implementing their pilot program. The Children's Health Insurance
Program Reauthorization Act (CHIPRA) was enacted February 4, 2009.
Sections 203 and 601 of the CHIPRA relate to MEQC. 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 requirements. Section 601 of the CHIPRA, among
other things, requires a new final rule for the Payment Error Rate
Measurement (PERM) program and 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. We review, either directly or
through its contractors, of the sampling plans helps to ensure States
are using valid statistical methods for sample selection. The
collection of information is also necessary to 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. Form Number: CMS-317 (OMB control number: 0938-0146);
Frequency: Semi-Annually Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 10; Total Annual Responses: 20;
Total Annual Hours: 480. (For policy questions regarding this
collection contact Bridgett Rider at 410-786-2602.)
2. Type of Information Collection Request: Extension of a currently
approved collection; Title of
[[Page 20645]]
Information Collection: State Medicaid Eligibility Quality Control
(MEQC) Sample Selection Lists; Use: The MEQC system is based on monthly
State reviews of Medicaid and Medicaid expansion under Title XXI cases
by States performing the traditional sampling process identified
through statistically reliable statewide samples of cases selected from
the eligibility files. These reviews are conducted to determine whether
or not the sampled cases meet applicable State Title XIX or XXI
eligibility requirements when applicable. The reviews are also used to
assess beneficiary liability, if any, and to determine the amounts paid
to provide Medicaid services for these cases. In the MEQC system,
sampling is the only practical method of validating eligibility of the
total caseload and determining the dollar value of eligibility
liability errors. Any attempt to make such validations and
determinations by reviewing every case would be an enormous and
unwieldy undertaking. At the beginning of each month, State agencies
still performing the traditional sample are required to submit sample
selection lists which identify all of the cases selected for review in
the States' samples. The sample selection lists contain identifying
information on Medicaid beneficiaries such as: State agency review
number, beneficiary's name and address, the name of the county where
the beneficiary resides, Medicaid case number, etc. The submittal of
the sample selection lists is necessary for Regional Office validation
of State reviews. Without these lists, the integrity of the sampling
results would be suspect and the Regional Offices would have no data on
the adequacy of the States' monthly sample draw or review completion
status. The authority for collecting this information is Section
1903(u) of the Social Security Act. The specific requirement for
submitting sample selection lists is described in regulations at 42 CFR
431.814(h). Regional Office staff review the sample selection lists to
determine that States are sampling a sufficient number of cases for
review. Form Number: CMS-319 (OMB control number: 0938-0147);
Frequency: Monthly; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 10; Total Annual Responses: 120;
Total Annual Hours: 960. (For policy questions regarding this
collection contact Bridgett Rider at 410-786-2602.)
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Payment Error
Rate Measurement in Medicaid & Children's Health Insurance Program
(CHIP); Use: The Improper Payments Information Act (IPIA) of 2002 as
amended by the Improper Payments Elimination and Recovery Improvement
Act (IPERIA) of 2012 requires CMS to produce national error rates for
Medicaid and Children's Health Insurance Program (CHIP). To comply with
the IPIA, CMS will engage a Federal contractor to produce the error
rates in Medicaid and CHIP. The error rates for Medicaid and CHIP are
calculated based on the reviews on three components of both Medicaid
and CHIP program. They are: Fee-for-service claims medical reviews and
data processing reviews, managed care claims data-processing reviews,
and eligibility reviews. Each of the review components collects
different types of information, and the state-specific error rates for
each of the review components will be used to calculate an overall
state-specific error rate, and the individual state-specific error
rates will be used to produce a national error rate for Medicaid and
CHIP. The states will be requested to submit, at their option, test
data which include full claims details to the contractor prior to the
quarterly submissions to detect potential problems in the dataset to
and ensure the quality of the data. These states will be required to
submit quarterly claims data to the contractor who will pull a
statistically valid random sample, each quarter, by strata, so that
medical and data processing reviews can be performed. State-specific
error rates will be based on these review results. We need to collect
the fee-for-service claims data, medical policies, and other
information from states as well as medical records from providers in
order for the contractor to sample and review adjudicated claims in
those states selected for medical reviews and data processing reviews.
Based on the reviews, state-specific error rates will be calculated
which will serve as part of the basis for calculating national Medicaid
and CHIP error rates. Form Number: CMS-10166 (OMB control number: 0938-
0974); Frequency: Annually, Quarterly; Affected Public: State, Local,
or Tribal Governments; Number of Respondents: 34; Total Annual
Responses: 34; Total Annual Hours: 56,100. (For policy questions
regarding this collection contact Bridgett Rider at 410-786-2602.)
4. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Medicaid and
Children's Health Insurance (CHIP) Managed Care Claims and Related
Information; Use: The Payment Error Rate Measurement (PERM) program
measures improper payments for Medicaid and the State Children's Health
Insurance Program (SCHIP). The program was designed to comply with the
Improper Payments Information Act (IPIA) of 2002 and the Office of
Management and Budget (OMB) guidance. Although OMB guidance requires
error rate measurement for SCHIP, 2009 SCHIP legislation temporarily
suspended PERM measurement for this program and changed to Children's
Health Insurance Program (CHIP) effective April 01, 2009. See
Children's Health Insurance Program Reauthorization Act of 2009
(CHIPRA) Public Law 111-3 for more details. There are two phases of the
PERM program, the measurement phase and the corrective action phase.
The PERM measures improper payments in Medicaid and CHIP and produces
State and national-level error rates for each program. The error rates
are based on reviews of Medicaid and CHIP fee-for-service (FFS) and
managed care payments made in the Federal fiscal year under review.
States conduct eligibility reviews and report eligibility related
payment error rates also used in the national error rate calculation.
We created a 17 State rotation cycle so that each State will
participate in PERM once every three years. Following is the list of
States in which we will measure improper payments over the next three
years in Medicaid. We need to collect capitation payment information
from the selected States so that the federal contractor can draw a
sample and review the managed care capitation payments. We will also
collect State managed care contracts, rate schedules and updates to the
contracts and rate schedules. This information will be used by the
Federal contractor when conducting the managed care claims reviews.
Sections 1902(a)(6) and 2107(b)(1) of the Social Security Act grants
CMS authority to collect information from the States. The IPIA requires
us to produce national error rates in Medicaid and CHIP fee-for-
service, including the managed care component. The State-specific
Medicaid managed care and CHIP managed care error rates will be based
on reviews of managed care capitation payments in each program and will
be used to produce national Medicaid managed care and CHIP managed care
error rates. Form Number: CMS-10178 (OMB control number: 0938-0994);
Frequency: Occasionally; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 34; Total Annual
[[Page 20646]]
Responses: 28,050; Total Annual Hours: 28,050. (For policy questions
regarding this collection contact Bridgett Rider at 410-786-2602.)
5. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Eligibility Error
Rate Measurement in Medicaid and the Children's Health Insurance
Program; Use: The Improper Payments Information Act (IPIA) of 2002
requires CMS to produce national error rates for Medicaid and the
Children's Health Insurance Program (CHIP). To comply with the IPIA,
CMS will use a national contracting strategy to produce error rates for
Medicaid and CHIP fee-for-service and managed care improper payments.
The federal contractor will review States on a rotational basis so that
each State will be measured for improper payments, in each program,
once and only once every three years. Subsequent to the first
publication, we determined that we will measure Medicaid and CHIP in
the same State. Therefore, States will measure Medicaid and CHIP
eligibility in the same year measured for fee-for-service and managed
care. We believe this approach will advantage States through economies
of scale (e.g. administrative ease and shared staffing for both
programs reviews). We also determined that interim case completion
timeframes and reporting are critical to the integrity of the reviews
and to keep the reviews on schedule to produce a timely error rate.
Lastly, the sample sizes were increased slightly in order to produce an
equal sample size per strata each month. Periodically, CMS will conduct
Federal re-reviews of States' PERM files to ensure the accuracy of
States' review findings and the validity of the review process. CMS
will select a random subsample of Medicaid and CHIP cases from the
sample selection lists provided by each State. States will submit all
pertinent information related to the review of each sampled case that
is selected by CMS. Form Number: CMS-10184 (OMB control number: 0938-
1012); Frequency: Annually, Quarterly Affected Public: State, Local, or
Tribal Governments; Number of Respondents: 34; Total Annual Responses:
1,583; Total Annual Hours: 946,164. (For policy questions regarding
this collection contact Bridgett Rider at 410-786-2602.)
Dated: April 5, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2016-08106 Filed 4-7-16; 8:45 am]
BILLING CODE 4120-01-P