Agency Information Collection Activities: Submission for OMB Review; Comment Request, 78438-78439 [2014-30468]
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78438
Federal Register / Vol. 79, No. 249 / Tuesday, December 30, 2014 / Notices
SUPPLEMENTARY INFORMATION:
Change in Standard Procedure
GSA posts the POV mileage
reimbursement rates, formerly
published in 41 CFR Chapter 301, solely
on the internet at www.gsa.gov/mileage.
Also, posted on this site is the standard
mileage rate for moving purposes. This
process, implemented in FTR
Amendments 2010–07, 75 FR 72965,
November 29, 2010, 2007–03, 72 FR
35187, June 27, 2007, and 2007–06, 72
FR 70234, December 11, 2007, in the
Federal Register ensures more timely
updates in mileage reimbursement rates
by GSA for Federal employees who are
on official travel or relocating. Notices
published periodically in the Federal
Register, such as this one, and the
changes posted on the GSA Web site,
now constitute the only notification to
Federal agencies of revisions to the POV
mileage reimbursement rates and the
standard mileage reimbursement rate for
moving purposes.
Dated: December 16, 2014.
Alexander J. Kurien,
Deputy Associate Administrator, Office of
Asset and Transportation Management,
Office of Government-Wide Policy.
[FR Doc. 2014–30317 Filed 12–29–14; 8:45 am]
BILLING CODE 6820–14–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10421]
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
(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
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including any of the
following subjects: (1) The necessity and
utility of the proposed information
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SUMMARY:
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21:42 Dec 29, 2014
Jkt 235001
Under the
Paperwork Reduction Act of 1995 (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 (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-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 that summarizes
the following proposed collection(s) of
information for public comment:
SUPPLEMENTARY INFORMATION:
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
ACTION:
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 on the collection(s) of
information must be received by the
OMB desk officer by January 29, 2015.
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions:
OMB, Office of Information and
Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number: (202) 395–5806 or
Email: OIRA_submission@omb.eop.gov.
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.
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1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Fee-for-Service
Recovery Audit Prepayment Review
Demonstration and Prior Authorization
Demonstration; Use: On July 23, 2012,
the Office of Management and Budget
approved the collections required for
two demonstrations of prepayment
review and prior authorization. The first
demonstration allows Medicare
Recovery Auditors to review claims on
a pre-payment basis in certain States.
The second demonstration established a
prior authorization program for Power
Mobility Device claims in certain States.
For the Recovery Audit Prepayment
Review Demonstration, CMS and its
agents request additional
documentation, including medical
records, to support submitted claims. As
discussed in more detail in Chapter 3 of
the Program Integrity Manual,
additional documentation includes any
medical documentation, beyond what is
included on the face of the claim that
supports the item or service that is
billed. For Medicare to consider
coverage and payment for any item or
service, the information submitted by
the provider or supplier (e.g., claims)
must be supported by the
documentation in the patient’s medical
records. When conducting complex
medical review, the contractor specifies
documentation they require in
accordance with Medicare’s rules and
policies. In addition, providers and
suppliers may supply additional
documentation not explicitly listed by
the contractor. This supporting
information may be requested by CMS
and its agents on a routine basis in
instances where diagnoses on a claim do
not clearly indicate medical necessity,
or if there is a suspicion of fraud.
For the Prior Authorization of Power
Mobility Devices (PMDs)
Demonstration, we are piloting prior
authorization for PMDs. Prior
authorization will allow the applicable
documentation that supports a claim to
be submitted before the item is
delivered. For prior authorization,
relevant documentation for review is
submitted before the item is delivered or
the service is rendered. CMS will
conduct this demonstration in
California, Florida, Illinois, Michigan,
New York, North Carolina, Texas,
Pennsylvania, Ohio, Louisiana,
Missouri, Maryland, New Jersey,
Indiana, Kentucky, Georgia, Tennessee,
Washington, and Arizona based on
beneficiary address as reported to the
Social Security Administration and
recorded in the Common Working File
(CWF). For the demonstration, a prior
E:\FR\FM\30DEN1.SGM
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Federal Register / Vol. 79, No. 249 / Tuesday, December 30, 2014 / Notices
authorization request can be completed
by the (ordering) physician or treating
practitioner and submitted to the
appropriate DME MAC for an initial
decision. The supplier may also submit
the request on behalf of the physician or
treating practitioner. The physician,
treating practitioner or supplier who
submits the request on behalf of the
physician or treating practitioner, is
referred to as the ‘‘submitter.’’ Under
this demonstration, the submitter will
submit to the DME MAC a request for
prior authorization and all relevant
documentation to support Medicare
coverage of the PMD item. Form
Number: CMS–10421 (OMB control
number: 0938–1169); Frequency:
Occasionally; Affected Public: State,
Local or Tribal Governments; Number of
Respondents: 333,750; Total Annual
Responses: 333,750; Total Annual
Hours: 170,060. (For policy questions
regarding this collection contact Daniel
Schwartz at 410–786–4197.)
Dated: December 23, 2014.
Martique Jones,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2014–30468 Filed 12–29–14; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3296–FN]
RIN 0938–ZB14
Medicare Program; Evaluation Criteria
and Standards for Beneficiary and
Family Centered Care Quality
Improvement Organization Contract
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Final notice.
AGENCY:
This final notice announces
the general criteria we will use to
evaluate the effectiveness and efficiency
of Beneficiary and Family Centered Care
(BFCC) Quality Improvement
Organizations (QIOs) that entered into
contracts with CMS under the 11th
Statement of Work (SOW) in May 2014.
The activities for the BFCC–QIO SOW
began August 1, 2014. (This contract
allows for a transition period from the
incumbent QIOs to the successor QIOs.)
In addition, this notice addresses the
public comments received on the July
28, 2014 notice with comment period
entitled, ‘‘Evaluation Criteria and
Standards for Beneficiary and Family
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SUMMARY:
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Centered Care Quality Improvement
Organization Contracts.’’
DATES: Effective Dates: August 1, 2014
to July 31, 2019.
FOR FURTHER INFORMATION CONTACT:
Alfreda Staton, (410) 786–4194.
SUPPLEMENTARY INFORMATION:
I. Background
Section 1153(h)(2) of the Social
Security Act (the Act) requires the
Secretary of the Department of Health
and Human Services (the Secretary) to
publish in the Federal Register the
general criteria and standards that will
be used to evaluate the effective and
efficient performance of contract
obligations by the Quality Improvement
Organizations (QIOs) and to provide the
opportunity for public comment with
respect to these criteria and standards.
II. Provisions of the Notice With
Comment Period
On July 28, 2014, we published a
notice with comment period in the
Federal Register (79 FR 43747 through
43749) entitled, ‘‘Evaluation Criteria
and Standards for Beneficiary and
Family Centered Care Quality
Improvement Organization Contracts,’’
announcing the general criteria we
would use to evaluate the effectiveness
and efficiency of Beneficiary and Family
Centered Care (BFCC) Quality
Improvement Organizations (QIOs) that
entered into contracts with CMS under
the 11th Statement of Work (SOW) in
May 2014 (HHSM–500–2014–RFP–
BFCC–QIO). That notice generally
summarized the tasks of the BFCC–QIOs
and the criteria to be used for annual
performance evaluations during the 5year term of the contract. BFCC–QIO
performance under the 11th SOW
contract began on August 1, 2014, after
a transition period.
The tasks of the BFCC–QIOs under
the BFCC–QIO 11th SOW contract are as
follows:
• Quality of care reviews, including
beneficiary complaint and general
quality of care reviews.
• Beneficiary appeals of denials of
hospital admissions discharge and
terminations of services decisions
commonly referred to as Grijalva, BIPA,
and Weichardt appeals.
• Medical necessity reviews.
• Appropriateness of setting reviews.
• Diagnosis Related Group (DRG)
reviews.
• Readmission reviews.
• Reviews under Emergency Medical
Treatment and Active Labor Act
(EMTALA).
• Sanctions.
• Monitoring of Physician
Acknowledgement Statements under
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78439
section 1156(a) of the Act and our
regulations at 42 CFR 412.46.
Evaluation of the Tasks Measures
The measures of BFCC–QIO
performance for the 11th SOW are as
follows:
• Quality of Review: Inter-Rater
Reliability.
• 4-day Data Entry Compliance.
• Timeliness of Beneficiary
Complaints and Other Quality of Care
Reviews.
• Timeliness of Discharge/Service
Termination Reviews.
• Timeliness of EMTALA and Higher
Weighted Diagnosis-Related Group
Reviews.
• Complainant Agreement to
Complete Survey.
• Beneficiary Experience with
Quality of Care Complaints.
• Beneficiary Experience with Appeal
Reviews.
Evaluation Criteria
The Annual and 54th Month
Evaluation Criteria for each of these
measures are specifically defined in
Attachment J–10, ‘‘Annual and 54th
Month Evaluation Criteria Measures
Table,’’ of the BFCC–QIO SOW; the
criteria for evaluating each deliverable
are identified in Schedule F of the 11th
SOW. Additional detail is provided in
the notice posted at: https://
www.gpo.gov/fdsys/pkg/FR-2014-07-28/
pdf/2014-17625.pdf.
III. Analysis of and Responses to Public
Comments on the Notice With Comment
Period
Two commenters submitted several
comments concerning the general
criteria we would use to evaluate the
effectiveness and efficiency of BFCC–
QIOs that will enter into contracts with
CMS under the 11th SOW. One
commenter was affiliated with a private
healthcare quality improvement entity
and the other commenter was with a
healthcare quality improvement
association. A summary of the
comments and our responses are as
follows:
Comment: Both commenters
expressed concern with potential public
perception of bias arising from the
evaluation criterion that considers of
beneficiary experience with the quality
of care complaints and appeal reviews
as part of the evaluation of the BFCC–
QIO’s performance of quality-of-care
and other statutory and regulatory
reviews and appeals. The commenters
indicated that consideration of
beneficiary experience with the quality
of care complaints and appeal reviews
as part of the evaluation of the BFCC–
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Agencies
[Federal Register Volume 79, Number 249 (Tuesday, December 30, 2014)]
[Notices]
[Pages 78438-78439]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-30468]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10421]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
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 (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 a second opportunity
for public comment on the notice. Interested persons are invited to
send comments regarding the burden estimate 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 on the collection(s) of information must be received by
the OMB desk officer by January 29, 2015.
ADDRESSES: When commenting on the proposed information collections,
please reference the document identifier or OMB control number. To be
assured consideration, comments and recommendations must be received by
the OMB desk officer via one of the following transmissions:
OMB, Office of Information and Regulatory Affairs, Attention: CMS
Desk Officer, Fax Number: (202) 395-5806 or Email:
OIRA_submission@omb.eop.gov.
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: Under the Paperwork Reduction Act of 1995
(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 (44 U.S.C. 3506(c)(2)(A)) requires
federal agencies to publish a 30-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 that
summarizes the following proposed collection(s) of information for
public comment:
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Fee-for-Service
Recovery Audit Prepayment Review Demonstration and Prior Authorization
Demonstration; Use: On July 23, 2012, the Office of Management and
Budget approved the collections required for two demonstrations of
prepayment review and prior authorization. The first demonstration
allows Medicare Recovery Auditors to review claims on a pre-payment
basis in certain States. The second demonstration established a prior
authorization program for Power Mobility Device claims in certain
States.
For the Recovery Audit Prepayment Review Demonstration, CMS and its
agents request additional documentation, including medical records, to
support submitted claims. As discussed in more detail in Chapter 3 of
the Program Integrity Manual, additional documentation includes any
medical documentation, beyond what is included on the face of the claim
that supports the item or service that is billed. For Medicare to
consider coverage and payment for any item or service, the information
submitted by the provider or supplier (e.g., claims) must be supported
by the documentation in the patient's medical records. When conducting
complex medical review, the contractor specifies documentation they
require in accordance with Medicare's rules and policies. In addition,
providers and suppliers may supply additional documentation not
explicitly listed by the contractor. This supporting information may be
requested by CMS and its agents on a routine basis in instances where
diagnoses on a claim do not clearly indicate medical necessity, or if
there is a suspicion of fraud.
For the Prior Authorization of Power Mobility Devices (PMDs)
Demonstration, we are piloting prior authorization for PMDs. Prior
authorization will allow the applicable documentation that supports a
claim to be submitted before the item is delivered. For prior
authorization, relevant documentation for review is submitted before
the item is delivered or the service is rendered. CMS will conduct this
demonstration in California, Florida, Illinois, Michigan, New York,
North Carolina, Texas, Pennsylvania, Ohio, Louisiana, Missouri,
Maryland, New Jersey, Indiana, Kentucky, Georgia, Tennessee,
Washington, and Arizona based on beneficiary address as reported to the
Social Security Administration and recorded in the Common Working File
(CWF). For the demonstration, a prior
[[Page 78439]]
authorization request can be completed by the (ordering) physician or
treating practitioner and submitted to the appropriate DME MAC for an
initial decision. The supplier may also submit the request on behalf of
the physician or treating practitioner. The physician, treating
practitioner or supplier who submits the request on behalf of the
physician or treating practitioner, is referred to as the
``submitter.'' Under this demonstration, the submitter will submit to
the DME MAC a request for prior authorization and all relevant
documentation to support Medicare coverage of the PMD item. Form
Number: CMS-10421 (OMB control number: 0938-1169); Frequency:
Occasionally; Affected Public: State, Local or Tribal Governments;
Number of Respondents: 333,750; Total Annual Responses: 333,750; Total
Annual Hours: 170,060. (For policy questions regarding this collection
contact Daniel Schwartz at 410-786-4197.)
Dated: December 23, 2014.
Martique Jones,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. 2014-30468 Filed 12-29-14; 8:45 am]
BILLING CODE 4120-01-P