Agency Information Collection Activities: Submission for OMB Review; Comment Request, 66031-66033 [2016-23157]
Download as PDF
66031
Federal Register / Vol. 81, No. 186 / Monday, September 26, 2016 / Notices
comments should be received within 30
days of this notice.
Proposed Project
Aggregate Reports for Tuberculosis
Program Evaluation (OMB Control
Number 0920–0457)—Reinstatement
Without Change of a Previously
Approved Collection—National Center
for HIV/AIDS, Viral Hepatitis, STD, and
TB Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC, NCHHSTP, Division of
Tuberculosis Elimination (DTBE)
proposes a reinstatement without
change of the Aggregate Reports for
Tuberculosis Program Evaluation,
previously approved under OMB
Control Number 0920–0457. This
request is for a three-year clearance.
There are no revisions to the report
forms, data definitions, or reporting
instructions.
DTBE is the lead agency for
tuberculosis elimination in the United
States. To ensure the elimination of
tuberculosis in the United States, CDC
monitors indicators for key program
activities, such as finding tuberculosis
infections in recent contacts of cases
and in other persons likely to be
infected and providing therapy for
latent tuberculosis infection.
In 2000, CDC implemented two
program evaluation reports for annual
submission: Aggregate report of followup for contacts of tuberculosis, and
Aggregate report of screening and
preventive therapy for tuberculosis
infection (OMB No. 0920–0457). The
respondents for these reports were the
68 state and local tuberculosis control
programs receiving federal cooperative
agreement funding through DTBE. This
group will also respond to this
collection of information.
These Aggregate reports emphasize
treatment outcomes, high-priority target
populations vulnerable to tuberculosis,
and programmed electronic report entry,
which transitioned to the National
Tuberculosis Indicators Project (NTIP), a
secure web-based system for program
evaluation data, in 2010. No other
federal agency collects this type of
national tuberculosis data, and the
Aggregate report of follow-up for
contacts of tuberculosis, and Aggregate
report of screening and preventive
therapy for tuberculosis infection are
the only data source about latent
tuberculosis infection for monitoring
national progress toward tuberculosis
elimination with these activities.
CDC provides ongoing assistance in
the preparation and utilization of these
reports at the local and state levels of
public health jurisdiction. CDC also
provides respondents with technical
support for NTIP access (Electronic—
100%, Use of Electronic Signatures).
The annual burden to respondents is
estimated to be 226 hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Data clerks and Program Managers
(electronic).
Program Managers (manual) ............
Data clerks (manual) .........................
Data clerks and Program Managers
(electronic).
Program Managers (manual) ............
Data clerks (manual) .........................
Number of
responses per
respondent
Tuberculosis
100
1
30/60
Tuberculosis
18
1
30/60
Tuberculosis
18
1
3
Tuberculosis
100
1
30/60
Tuberculosis
18
1
30/60
Tuberculosis
Follow-up and Treatment of Contacts to
Cases Form.
Follow-up and Treatment of Contacts to
Cases Form.
Follow-up and Treatment of Contacts to
Cases Form.
Targeted Testing and Treatment for Latent
Infection.
Targeted Testing and Treatment for Latent
Infection.
Targeted Testing and Treatment for Latent
Infection.
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2016–23072 Filed 9–23–16; 8:45 am]
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1
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–R–70, CMS–R–
72, CMS–R–247, CMS–10062, CMS–10268,
CMS–10615 and CMS–10623]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services.
ACTION: Notice.
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AGENCY:
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
SUMMARY:
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PO 00000
Frm 00037
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Average
burden per
response
(in hours)
Number of
respondents
Form name
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.
E:\FR\FM\26SEN1.SGM
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66032
Federal Register / Vol. 81, No. 186 / Monday, September 26, 2016 / Notices
Comments on the collection(s) of
information must be received by the
OMB desk officer by October 26, 2016.
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_s 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: Information
Collection Requirements in HSQ–110,
Acquisition, Protection and Disclosure
of Peer review Organization Information
and Supporting Regulations; Use: The
Peer Review Improvement Act of 1982
authorizes quality improvement
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DATES:
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19:40 Sep 23, 2016
Jkt 238001
organizations (QIOs), formally known as
peer review organizations (PROs), to
acquire information necessary to fulfill
their duties and functions and places
limits on disclosure of the information.
The QIOs are required to provide
notices to the affected parties when
disclosing information about them.
These requirements serve to protect the
rights of the affected parties. The
information provided in these notices is
used by the patients, practitioners and
providers to: Obtain access to the data
maintained and collected on them by
the QIOs; add additional data or make
changes to existing QIO data; and reflect
in the QIO’s record the reasons for the
QIO’s disagreeing with an individual’s
or provider’s request for amendment.
Form Number: CMS–R–70 (OMB control
number: 0938–0426); Frequency:
Reporting—On occasion; Affected
Public: Business or other for-profits;
Number of Respondents: 400; Total
Annual Responses: 21,200; Total
Annual Hours: 42,400. (For policy
questions regarding this collection
contact Winsome Higgins at 410–786–
1835.)
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Information
Collection Requirements in 42 CFR
478.18, 478.34, 478.36, 478.42, QIO
Reconsiderations and Appeals; Use: In
the event that a beneficiary, provider,
physician, or other practitioner does not
agree with the initial determination of a
Quality Improvement Organization
(QIO) or a QIO subcontractor, it is
within that party’s rights to request
reconsideration. The information
collection requirements 42 CFR 478.18,
478.34, 478.36, and 478.42, contain
procedures for QIOs to use in
reconsideration of initial
determinations. The information
requirements contained in these
regulations are on QIOs to provide
information to parties requesting the
reconsideration. These parties will use
the information as guidelines for appeal
rights in instances where issues are
actively being disputed. Form Number:
CMS–R–72 (OMB control number:
0938–0443); Frequency: Reporting—On
occasion; Affected Public: Individuals or
Households and Business or other forprofit institutions; Number of
Respondents: 2,590; Total Annual
Responses: 5,228; Total Annual Hours:
2,822. (For policy questions regarding
this collection contact Winsome Higgins
at 410–786–1835.)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Expanded
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Coverage for Diabetes Outpatient SelfManagement Training Services and
Supporting Regulations; Use: According
to the National Health and Nutrition
Examination Survey (NHANES), as
many as 18.7 percent of Americans over
age 65 are at risk for developing
diabetes. The goals in the management
of diabetes are to achieve normal
metabolic control and reduce the risk of
micro- and macro-vascular
complications. Numerous epidemiologic
and interventional studies point to the
necessity of maintaining good glycemic
control to reduce the risk of the
complications of diabetes. Despite this
knowledge, diabetes remains the leading
cause of blindness, lower extremity
amputations and kidney disease
requiring dialysis. Diabetes and its
complications are primary or secondary
factors in an estimated 9 percent of
hospitalizations (Aubert, RE, et al.,
Diabetes-related hospitalizations and
hospital utilization. In: Diabetes in
America. 2nd ed. National Institutes of
Health, National Institute of Diabetes
and Digestive and Kidney Disease, NIH,
Pub. No 95–1468–1995: 553–570).
Overall, beneficiaries with diabetes are
hospitalized 1.5 times more often than
beneficiaries without diabetes. HCFA–
3002–F provided for uniform coverage
of diabetes outpatient self-management
training services. These services include
educational and training services
furnished to a beneficiary with diabetes
by an entity approved to furnish the
services. The physician or qualified
non-physician practitioner treating the
beneficiary’s diabetes would certify that
these services are needed as part of a
comprehensive plan of care. This rule
established the quality standards that an
entity would be required to meet in
order to participate in furnishing
diabetes outpatient self-management
training services. It set forth payment
amounts that have been established in
consultation with appropriate diabetes
organizations. It implements section
4105 of the Balanced Budget Act of
1997. Form Number: CMS–R–247 (OMB
control number: 0938–0818); Frequency:
Recordkeeping and Reporting—
Occasionally; Affected Public: Business
or other for-profit institutions; Number
of Respondents: 5,327; Total Annual
Responses: 63,924; Total Annual Hours:
197,542. (For policy questions regarding
this collection contact Kristin Shifflett
at 410–786–4133.)
4. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Collection of
Diagnostic Data from Medicare
Advantage Organizations for Risk
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Federal Register / Vol. 81, No. 186 / Monday, September 26, 2016 / Notices
Adjusted Payments; Use: CMS requires
hospital inpatient, hospital outpatient
and physician diagnostic data from
Medicare Advantage (MA) organizations
to continue making payment under the
risk adjustment methodology. CMS will
use the data to make risk adjusted
payment under Parts C and D. MA and
MA–PD plans will use the data to
develop their Part C and D bids. As
required by law, CMS also annually
publishes the risk adjustment factors for
plans and other interested entities in the
Advance Notice of Methodological
Changes for MA Payment Rates (every
February) and the Announcement of
Medicare Advantage Payment Rates
(every April). Lastly, CMS issues
monthly reports to each individual plan
that contains the CMS Hierarchical
Condition Category (HCC) and RxHCC
models’ output and the risk scores and
reimbursements for each beneficiary
that is enrolled in their plan. Form
Number: CMS–10062 (OMB control
number: 0938–0878); Frequency:
Quarterly; Affected Public: Private
sector (Business or other for profit and
Not-for-profit institutions); Number of
Respondents: 691; Total Annual
Responses: 83,000,000; Total Annual
Hours: 40,650. (For policy questions
regarding this collection contact
Michael P. Massimini at 410–786–1566.)
5. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Consolidated
Renal Operations in a Web Enabled
Network (CROWNWeb) Third-party
Submission Authorization Form; Use:
The Consolidated Renal Operations in a
Web Enabled Network (CROWNWeb)
Third-Party Submission Authorization
form (CWTPSA) is to be completed by
‘‘Facility Administrators’’
(administrators of CMS-certified dialysis
facilities) if they intend to authorize a
third party (a business with which the
facility is associated, or an independent
vendor) to submit data to us to comply
with the recently-revised Conditions for
Coverage of dialysis facilities. The
CROWNWeb system is the system used
as the collection point of data necessary
for entitlement of ESRD patients to
Medicare benefits and for federal
government monitoring and assessing of
the quality and types of care provided
to renal patients. The information
collected through the CWTPSA form
will allow us along with our contractors
to receive data from authorized parties
acting on behalf of CMS-certified
dialysis facilities. Since February 2009,
we have received 4,160 CWTPSA forms
and anticipates that they will continue
to receive no more than 400 new
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Jkt 238001
CWTPSA forms annually to address the
creation of new facilities under the
current participating ‘‘third party
submitters.’’ Form Number: CMS–10268
(OMB control number: 0938–1052);
Frequency: Occasionally; Affected
Public: Business or other for-profits and
Not-for-profit institutions; Number of
Respondents: 400; Total Annual
Responses: 400; Total Annual Hours:
34. (For policy questions regarding this
collection contact Victoria Schlining at
410–786–6878.)
6. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Healthy Indiana
Program (HIP) 2.0 Beneficiaries Survey,
Focus Groups, and Informational
Interviews; Use: The collected
information will be used to make
decisions about the renewal of
precedent-setting waivers of Medicaid
policy that assure important beneficiary
protections regarding coverage and
access to care; e.g., the State of Indiana’s
non-emergency medical transportation
waiver which will end or will be
extended by no later than December 1,
2016. To support CMS decision making,
the collection’s survey effort would
provide more detailed information on
the Healthy Indiana Program (HIP) 2.0
demonstration’s beneficiary
understanding and experiences (current
and new enrollees as well as
disenrollees/lockouts). Additional
information on other key policies under
the demonstration, such as the 60-day
beneficiary lock-out period, is also
included in this information collection
request.
This request does not propose any
new or revised information collection
requirements or burden estimates
outside of what is currently approved by
OMB. Rather, it seeks to extend the
collection’s current expiration date of
September 30, 2016 (approved under
the emergency PRA process on March
21, 2016; see 81 FR 17460 dated March
29, 2106, and 81 FR 26798 dated May
4, 2016). Since the collection has
already been subject to the public
comment process for collection
activities taking place through
September 30, 2016, this ‘‘Extension of
a currently approved collection’’ will
only consider comments for activities
taking place from October 1, 2016,
through the end of the revised
expiration date. The revised expiration
date will be made available upon OMB
approval at reginfo.gov. Form Number:
CMS–10615 (OMB control number:
0938–1300); Frequency: Once; Affected
Public: Individuals and households,
Private sector (Business or other forprofits and Not-for-profits institutions),
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66033
and State, Local, or Tribal Governments;
Number of Respondents: 5,240; Total
Annual Responses: 5,240; Total Annual
Hours: 1,442. (For policy questions
regarding this collection contact Teresa
DeCaro at 202–384–6309.)
7. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Testing
Experience and Functional Tools
Demonstration: Personal Health Record
(PHR) User Survey; Use: The PHR user
survey is important to the TEFT
Program Evaluation and understanding
the impact of the TEFT PHR on
Medicaid CB–LTSS beneficiaries. The
TEFT evaluation team’s approach
includes monitoring state PHR
implementation efforts and fielding a
follow-up questionnaire to CB–LTSS
program participants that asks about
their experiences using the PHR. The
evaluation seeks to measure the degree
to which the PHR is implemented in an
accessible manner for Medicaid
beneficiaries of CB–LTSS. The survey
also is designed to assess the user
experience of the PHR, including access
and usability, as well as some measures
of user satisfaction and perceived
impacts of PHR use.
The information collection request
has been revised subsequent to the
publication of the 60-day Federal
Register notice on June 13, 2016 (81 FR
38187). Details can be found in the
package’s Supporting Statement. While
the June 13 Supporting Statement had
set out the correct number of burden
hours, the 60-day Federal Register
notice had inadvertently set out 192,113
hours. This should have been 206 hours.
Form Number: CMS–10623 (OMB
control number: 0938-New); Frequency:
Once; Affected Public: Individuals and
households; Number of Respondents:
576; Total Annual Responses: 576; Total
Annual Hours: 190. (For policy
questions regarding this collection
contact Kerry Lida at 410–786–4826.)
Dated: September 21, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–23157 Filed 9–23–16; 8:45 am]
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Agencies
[Federal Register Volume 81, Number 186 (Monday, September 26, 2016)]
[Notices]
[Pages 66031-66033]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-23157]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-R-70, CMS-R-72, CMS-R-247, CMS-10062, CMS-
10268, CMS-10615 and CMS-10623]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services.
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.
[[Page 66032]]
DATES: Comments on the collection(s) of information must be received by
the OMB desk officer by October 26, 2016.
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: Information
Collection Requirements in HSQ-110, Acquisition, Protection and
Disclosure of Peer review Organization Information and Supporting
Regulations; Use: The Peer Review Improvement Act of 1982 authorizes
quality improvement organizations (QIOs), formally known as peer review
organizations (PROs), to acquire information necessary to fulfill their
duties and functions and places limits on disclosure of the
information. The QIOs are required to provide notices to the affected
parties when disclosing information about them. These requirements
serve to protect the rights of the affected parties. The information
provided in these notices is used by the patients, practitioners and
providers to: Obtain access to the data maintained and collected on
them by the QIOs; add additional data or make changes to existing QIO
data; and reflect in the QIO's record the reasons for the QIO's
disagreeing with an individual's or provider's request for amendment.
Form Number: CMS-R-70 (OMB control number: 0938-0426); Frequency:
Reporting--On occasion; Affected Public: Business or other for-profits;
Number of Respondents: 400; Total Annual Responses: 21,200; Total
Annual Hours: 42,400. (For policy questions regarding this collection
contact Winsome Higgins at 410-786-1835.)
2. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Information
Collection Requirements in 42 CFR 478.18, 478.34, 478.36, 478.42, QIO
Reconsiderations and Appeals; Use: In the event that a beneficiary,
provider, physician, or other practitioner does not agree with the
initial determination of a Quality Improvement Organization (QIO) or a
QIO subcontractor, it is within that party's rights to request
reconsideration. The information collection requirements 42 CFR 478.18,
478.34, 478.36, and 478.42, contain procedures for QIOs to use in
reconsideration of initial determinations. The information requirements
contained in these regulations are on QIOs to provide information to
parties requesting the reconsideration. These parties will use the
information as guidelines for appeal rights in instances where issues
are actively being disputed. Form Number: CMS-R-72 (OMB control number:
0938-0443); Frequency: Reporting--On occasion; Affected Public:
Individuals or Households and Business or other for-profit
institutions; Number of Respondents: 2,590; Total Annual Responses:
5,228; Total Annual Hours: 2,822. (For policy questions regarding this
collection contact Winsome Higgins at 410-786-1835.)
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Expanded Coverage
for Diabetes Outpatient Self-Management Training Services and
Supporting Regulations; Use: According to the National Health and
Nutrition Examination Survey (NHANES), as many as 18.7 percent of
Americans over age 65 are at risk for developing diabetes. The goals in
the management of diabetes are to achieve normal metabolic control and
reduce the risk of micro- and macro-vascular complications. Numerous
epidemiologic and interventional studies point to the necessity of
maintaining good glycemic control to reduce the risk of the
complications of diabetes. Despite this knowledge, diabetes remains the
leading cause of blindness, lower extremity amputations and kidney
disease requiring dialysis. Diabetes and its complications are primary
or secondary factors in an estimated 9 percent of hospitalizations
(Aubert, RE, et al., Diabetes-related hospitalizations and hospital
utilization. In: Diabetes in America. 2nd ed. National Institutes of
Health, National Institute of Diabetes and Digestive and Kidney
Disease, NIH, Pub. No 95-1468-1995: 553-570). Overall, beneficiaries
with diabetes are hospitalized 1.5 times more often than beneficiaries
without diabetes. HCFA-3002-F provided for uniform coverage of diabetes
outpatient self-management training services. These services include
educational and training services furnished to a beneficiary with
diabetes by an entity approved to furnish the services. The physician
or qualified non-physician practitioner treating the beneficiary's
diabetes would certify that these services are needed as part of a
comprehensive plan of care. This rule established the quality standards
that an entity would be required to meet in order to participate in
furnishing diabetes outpatient self-management training services. It
set forth payment amounts that have been established in consultation
with appropriate diabetes organizations. It implements section 4105 of
the Balanced Budget Act of 1997. Form Number: CMS-R-247 (OMB control
number: 0938-0818); Frequency: Recordkeeping and Reporting--
Occasionally; Affected Public: Business or other for-profit
institutions; Number of Respondents: 5,327; Total Annual Responses:
63,924; Total Annual Hours: 197,542. (For policy questions regarding
this collection contact Kristin Shifflett at 410-786-4133.)
4. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Collection of
Diagnostic Data from Medicare Advantage Organizations for Risk
[[Page 66033]]
Adjusted Payments; Use: CMS requires hospital inpatient, hospital
outpatient and physician diagnostic data from Medicare Advantage (MA)
organizations to continue making payment under the risk adjustment
methodology. CMS will use the data to make risk adjusted payment under
Parts C and D. MA and MA-PD plans will use the data to develop their
Part C and D bids. As required by law, CMS also annually publishes the
risk adjustment factors for plans and other interested entities in the
Advance Notice of Methodological Changes for MA Payment Rates (every
February) and the Announcement of Medicare Advantage Payment Rates
(every April). Lastly, CMS issues monthly reports to each individual
plan that contains the CMS Hierarchical Condition Category (HCC) and
RxHCC models' output and the risk scores and reimbursements for each
beneficiary that is enrolled in their plan. Form Number: CMS-10062 (OMB
control number: 0938-0878); Frequency: Quarterly; Affected Public:
Private sector (Business or other for profit and Not-for-profit
institutions); Number of Respondents: 691; Total Annual Responses:
83,000,000; Total Annual Hours: 40,650. (For policy questions regarding
this collection contact Michael P. Massimini at 410-786-1566.)
5. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Consolidated
Renal Operations in a Web Enabled Network (CROWNWeb) Third-party
Submission Authorization Form; Use: The Consolidated Renal Operations
in a Web Enabled Network (CROWNWeb) Third-Party Submission
Authorization form (CWTPSA) is to be completed by ``Facility
Administrators'' (administrators of CMS-certified dialysis facilities)
if they intend to authorize a third party (a business with which the
facility is associated, or an independent vendor) to submit data to us
to comply with the recently-revised Conditions for Coverage of dialysis
facilities. The CROWNWeb system is the system used as the collection
point of data necessary for entitlement of ESRD patients to Medicare
benefits and for federal government monitoring and assessing of the
quality and types of care provided to renal patients. The information
collected through the CWTPSA form will allow us along with our
contractors to receive data from authorized parties acting on behalf of
CMS-certified dialysis facilities. Since February 2009, we have
received 4,160 CWTPSA forms and anticipates that they will continue to
receive no more than 400 new CWTPSA forms annually to address the
creation of new facilities under the current participating ``third
party submitters.'' Form Number: CMS-10268 (OMB control number: 0938-
1052); Frequency: Occasionally; Affected Public: Business or other for-
profits and Not-for-profit institutions; Number of Respondents: 400;
Total Annual Responses: 400; Total Annual Hours: 34. (For policy
questions regarding this collection contact Victoria Schlining at 410-
786-6878.)
6. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Healthy Indiana
Program (HIP) 2.0 Beneficiaries Survey, Focus Groups, and Informational
Interviews; Use: The collected information will be used to make
decisions about the renewal of precedent-setting waivers of Medicaid
policy that assure important beneficiary protections regarding coverage
and access to care; e.g., the State of Indiana's non-emergency medical
transportation waiver which will end or will be extended by no later
than December 1, 2016. To support CMS decision making, the collection's
survey effort would provide more detailed information on the Healthy
Indiana Program (HIP) 2.0 demonstration's beneficiary understanding and
experiences (current and new enrollees as well as disenrollees/
lockouts). Additional information on other key policies under the
demonstration, such as the 60-day beneficiary lock-out period, is also
included in this information collection request.
This request does not propose any new or revised information
collection requirements or burden estimates outside of what is
currently approved by OMB. Rather, it seeks to extend the collection's
current expiration date of September 30, 2016 (approved under the
emergency PRA process on March 21, 2016; see 81 FR 17460 dated March
29, 2106, and 81 FR 26798 dated May 4, 2016). Since the collection has
already been subject to the public comment process for collection
activities taking place through September 30, 2016, this ``Extension of
a currently approved collection'' will only consider comments for
activities taking place from October 1, 2016, through the end of the
revised expiration date. The revised expiration date will be made
available upon OMB approval at reginfo.gov. Form Number: CMS-10615 (OMB
control number: 0938-1300); Frequency: Once; Affected Public:
Individuals and households, Private sector (Business or other for-
profits and Not-for-profits institutions), and State, Local, or Tribal
Governments; Number of Respondents: 5,240; Total Annual Responses:
5,240; Total Annual Hours: 1,442. (For policy questions regarding this
collection contact Teresa DeCaro at 202-384-6309.)
7. Type of Information Collection Request: New collection (Request
for a new OMB control number); Title of Information Collection: Testing
Experience and Functional Tools Demonstration: Personal Health Record
(PHR) User Survey; Use: The PHR user survey is important to the TEFT
Program Evaluation and understanding the impact of the TEFT PHR on
Medicaid CB-LTSS beneficiaries. The TEFT evaluation team's approach
includes monitoring state PHR implementation efforts and fielding a
follow-up questionnaire to CB-LTSS program participants that asks about
their experiences using the PHR. The evaluation seeks to measure the
degree to which the PHR is implemented in an accessible manner for
Medicaid beneficiaries of CB-LTSS. The survey also is designed to
assess the user experience of the PHR, including access and usability,
as well as some measures of user satisfaction and perceived impacts of
PHR use.
The information collection request has been revised subsequent to
the publication of the 60-day Federal Register notice on June 13, 2016
(81 FR 38187). Details can be found in the package's Supporting
Statement. While the June 13 Supporting Statement had set out the
correct number of burden hours, the 60-day Federal Register notice had
inadvertently set out 192,113 hours. This should have been 206 hours.
Form Number: CMS-10623 (OMB control number: 0938-New); Frequency: Once;
Affected Public: Individuals and households; Number of Respondents:
576; Total Annual Responses: 576; Total Annual Hours: 190. (For policy
questions regarding this collection contact Kerry Lida at 410-786-
4826.)
Dated: September 21, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2016-23157 Filed 9-23-16; 8:45 am]
BILLING CODE 4120-01-P