Agency Information Collection Activities: Proposed Collection: Public Comment Request Information Collection Request Title: Health Resources and Service Administration Uniform Data System, OMB No. 0915-0193-Revision, 29800-29801 [2018-13587]
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29800
Federal Register / Vol. 83, No. 123 / Tuesday, June 26, 2018 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS—Continued
Number of
respondents
Form name
Number of
responses per
respondent
Total
responses
Average
burden per
response
(in hours)
Total
burden
hours
National Survey of Organ Donation Attitudes and Practices—Web Online Panel (English and Spanish
Versions) ..........................................................................
8,000
1
8,000
.27
2,160
Total ..............................................................................
10,000
........................
10,000
........................
2,900
Amy P. McNulty,
Acting Director, Division of the Executive
Secretariat.
[FR Doc. 2018–13590 Filed 6–25–18; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request Information
Collection Request Title: Health
Resources and Service Administration
Uniform Data System, OMB No. 0915–
0193—Revision
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects of the Paperwork Reduction Act
of 1995, HRSA announces plans to
submit an Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting the ICR to
OMB, HRSA seeks comments from the
public regarding the burden estimate,
below, or any other aspect of the ICR.
DATES: Comments on this ICR must be
received no later than August 27, 2018.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 14N39, 5600 Fishers
Lane, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call Lisa Wright-Solomon, HRSA
Information Collection Clearance Officer
at (301) 443–1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
sradovich on DSK3GMQ082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:24 Jun 25, 2018
Jkt 244001
information request collection title for
reference.
Information Collection Request Title:
HRSA Uniform Data System (UDS),
OMB No. 0915–0193—Revision.
Abstract: HRSA utilizes the UDS for
annual reporting by certain HRSA
award recipients, including Health
Center Program awardees (those funded
under section 330 of the Public Health
Service (PHS) Act), Health Center
Program look-alikes, and Nurse
Education, Practice, Quality and
Retention (NEPQR) Program awardees
(specifically those funded under the
practice priority areas of section 831(b)
of the PHS Act).
Need and Proposed Use of the
Information: HRSA collects UDS data
annually to ensure compliance with
legislative and regulatory requirements,
improve clinical and operational
performance, and report overall program
accomplishments. These data help to
identify trends over time, enabling
HRSA to establish or expand targeted
programs and to identify effective
services and interventions that will
improve the health of medically
underserved communities. HRSA
compares UDS data with other national
health-related data sets to compare
HRSA award recipient patient
populations and the overall U.S.
population.
HRSA is considering several changes
for 2019 UDS data collection:
• Substance Use Disorder and Mental
Health Services: Collect substance use
disorder and mental health services by
provider specialty to better assess which
providers are delivering behavioral
health services; support investments in
these priority areas; and better describe
comprehensive, integrated models of
care.
• Closing the Referral Loop: Receipt
of Specialist Report (https://
ecqi.healthit.gov/ecqm/measures/
cms050v6t): Add a clinical quality
measure from the Centers for Medicare
and Medicaid Services (CMS)
electronic-specified clinical quality
measures to address care coordination.
• Health Information Technology
(health IT): Streamline and clarify
PO 00000
Frm 00060
Fmt 4703
Sfmt 4703
health IT questions regarding utilization
of health IT to include information
sharing, patient engagement, quality
improvement, and program evaluation
and research.
• Statin Therapy for the Prevention
and Treatment of Cardiovascular
Disease (https://ecqi.healthit.gov/ecqm/
measures/cms347v1): Replace the
current non-specified Coronary Artery
Disease measure with an e-specified
measure that aligns with the Centers for
Disease Control and Prevention and the
CMS Million Hearts® clinical quality
measures relating to statin therapy.
• Telemedicine and Virtual Visits:
Collect information on services
provided via telemedicine or virtual
visits by provider in order to capture the
changing health care delivery
landscape.
• Tenure for Health Center Staff:
Retire Table 5A related to the tenure for
staff.
• Workforce: Collect workforce
related information, including
workforce satisfaction and health
professional training.
Likely Respondents: The respondents
will include Health Center Program
awardees, Health Center Program lookalikes, and NEPQR Program awardees
funded under the practice priority areas
of section 831(b) of the PHS Act.
Burden Statement: Burden includes
the time expended by persons to
generate, maintain, retain, disclose or
provide the information requested. This
includes the time needed to review
instructions; to develop, acquire, install,
and utilize technology and systems for
the purpose of: Collecting, validating
and verifying information, processing
and maintaining information, disclosing
and providing information. It also
accounts for time to train personnel,
respond to a collection of information,
search data sources, complete and
review the collection of information,
and transmit or otherwise disclose the
information. The total annual burden
hours estimated for this ICR are
summarized in the table below.
E:\FR\FM\26JNN1.SGM
26JNN1
29801
Federal Register / Vol. 83, No. 123 / Tuesday, June 26, 2018 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Total
responses
Average
burden per
response
(in hours)
Total
burden
hours
Universal Report ..................................................................
Grant Report ........................................................................
1,471
504
1
1
1,471
504
223
30
328,033
15,120
Total ..............................................................................
1,975
........................
1,975
........................
343,153
HRSA specifically requests comments
on: (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.
Amy P. McNulty,
Acting Director, Division of the Executive
Secretariat.
[FR Doc. 2018–13587 Filed 6–25–18; 8:45 a.m.]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Heart, Lung, and Blood
Institute; Notice of Closed Meetings
sradovich on DSK3GMQ082PROD with NOTICES
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Heart, Lung,
and Blood Institute Special Emphasis Panel;
lncRNAs in HLBS Diseases.
Date: August 17, 2018.
Time: 8:30 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Crowne Plaza Washington National
Airport, 1480 Jefferson Davis Hwy, Arlington,
VA 22202.
Contact Person: Keith A. Mintzer, Ph.D.,
Scientific Review Officer, Office of Review
Branch/DERA, National Heart, Lung, and
Blood Institute, 6701 Rockledge Drive, Room
VerDate Sep<11>2014
17:24 Jun 25, 2018
Jkt 244001
7186, Bethesda, MD 20892–7924, 301–594–
7947 mintzerk@nhlbi.nih.gov.
Name of Committee: National Heart, Lung,
and Blood Institute Special Emphasis Panel;
MACS–WIHS DACC.
Date: August 21, 2018.
Time: 8:00 a.m. to 8:30 a.m.
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency Bethesda, One
Bethesda Metro Center, 7400 Wisconsin
Avenue, Bethesda, MD 20814.
Contact Person: Tony L. Creazzo, Ph.D.,
Scientific Review Officer, Office of Scientific
Review/DERA, National Heart, Lung, and
Blood Institute, National Institutes of Health,
6701 Rockledge Drive, Room 7180, Bethesda,
MD 20892–7924, 301–827–7913, creazzotl@
mail.nih.gov.
Name of Committee: National Heart, Lung,
and Blood Institute Special Emphasis Panel;
MACS–WIHS Clinical Research Sites.
Date: August 21, 2018.
Time: 8:30 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency Bethesda, One
Bethesda Metro Center, 7400 Wisconsin
Avenue, Bethesda, MD 20814.
Contact Person: Tony L. Creazzo, Ph.D.,
Scientific Review Officer, Office of Scientific
Review/DERA, National Heart, Lung, and
Blood Institute, National Institutes of Health,
6701 Rockledge Drive, Room 7180, Bethesda,
MD 20892–7924, 301–827–7913, creazzotl@
mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.233, National Center for
Sleep Disorders Research; 93.837, Heart and
Vascular Diseases Research; 93.838, Lung
Diseases Research; 93.839, Blood Diseases
and Resources Research, National Institutes
of Health, HHS)
Dated: June 19, 2018.
Michelle D. Trout,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2018–13633 Filed 6–25–18; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Heart, Lung, and Blood
Institute; Notice of Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
PO 00000
Frm 00061
Fmt 4703
Sfmt 4703
amended, notice is hereby given of the
following meetings of the NHLBI
Special Emphasis Panel.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
contract proposals and the discussions
could disclose confidential trade secrets
or commercial property such as
patentable material, and personal
information concerning individuals
associated with the grant applications
and contract proposals, the disclosure of
which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: National Heart, Lung,
and Blood Institute Special Emphasis Panel;
Career Development Program to Promote
Diversity in Health Research.
Date: July 13, 2018.
Time: 8:00 p.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: The William F. Bolger Center, 9600
Newbridge Drive, Potomac, MD 20854.
Contact Person: Michael P. Reilly, Ph.D.,
Scientific Review Officer, Office of Scientific
Review, National Heart, Lung, and Blood
Institute, National Institutes of Health, 6701
Rockledge Drive, Room 7200, Bethesda, MD
20892, 301–827–7975, reillymp@
nhlbi.nih.gov.
Name of Committee: National Heart, Lung,
and Blood Institute, Special Emphasis Panel;
Short-term Research Education to Increase
Diversity.
Date: July 20, 2018.
Time: 8:00 p.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: The William F. Bolger Center, 9600
Newbridge Drive, Potomac, MD 20854.
Contact Person: Lindsay M. Garvin, Ph.D.,
Scientific Review Officer, Office of Scientific
Review, National Heart, Lung, and Blood
Institute, National Institutes of Health, 6701
Rockledge Drive, Suite 7189, Bethesda, MD
20892, 301–827–7911, lindsay.garvin@
nih.gov.
Name of Committee: National Heart, Lung,
and Blood Institute Special Emphasis Panel;
NHLBI Mentored Career Development
Awards—K08 and K99.
Date: July 25, 2018.
Time: 1:00 p.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
E:\FR\FM\26JNN1.SGM
26JNN1
]]>Agencies
[Federal Register Volume 83, Number 123 (Tuesday, June 26, 2018)]
[Notices]
[Pages 29800-29801]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-13587]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request Information Collection Request Title: Health
Resources and Service Administration Uniform Data System, OMB No. 0915-
0193--Revision
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement for opportunity for public
comment on proposed data collection projects of the Paperwork Reduction
Act of 1995, HRSA announces plans to submit an Information Collection
Request (ICR), described below, to the Office of Management and Budget
(OMB). Prior to submitting the ICR to OMB, HRSA seeks comments from the
public regarding the burden estimate, below, or any other aspect of the
ICR.
DATES: Comments on this ICR must be received no later than August 27,
2018.
ADDRESSES: Submit your comments to [email protected] or mail the HRSA
Information Collection Clearance Officer, Room 14N39, 5600 Fishers
Lane, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
draft instruments, email [email protected] or call Lisa Wright-
Solomon, HRSA Information Collection Clearance Officer at (301) 443-
1984.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the information request collection title
for reference.
Information Collection Request Title: HRSA Uniform Data System
(UDS), OMB No. 0915-0193--Revision.
Abstract: HRSA utilizes the UDS for annual reporting by certain
HRSA award recipients, including Health Center Program awardees (those
funded under section 330 of the Public Health Service (PHS) Act),
Health Center Program look-alikes, and Nurse Education, Practice,
Quality and Retention (NEPQR) Program awardees (specifically those
funded under the practice priority areas of section 831(b) of the PHS
Act).
Need and Proposed Use of the Information: HRSA collects UDS data
annually to ensure compliance with legislative and regulatory
requirements, improve clinical and operational performance, and report
overall program accomplishments. These data help to identify trends
over time, enabling HRSA to establish or expand targeted programs and
to identify effective services and interventions that will improve the
health of medically underserved communities. HRSA compares UDS data
with other national health-related data sets to compare HRSA award
recipient patient populations and the overall U.S. population.
HRSA is considering several changes for 2019 UDS data collection:
Substance Use Disorder and Mental Health Services: Collect
substance use disorder and mental health services by provider specialty
to better assess which providers are delivering behavioral health
services; support investments in these priority areas; and better
describe comprehensive, integrated models of care.
Closing the Referral Loop: Receipt of Specialist Report
(https://ecqi.healthit.gov/ecqm/measures/cms050v6t): Add a clinical
quality measure from the Centers for Medicare and Medicaid Services
(CMS) electronic-specified clinical quality measures to address care
coordination.
Health Information Technology (health IT): Streamline and
clarify health IT questions regarding utilization of health IT to
include information sharing, patient engagement, quality improvement,
and program evaluation and research.
Statin Therapy for the Prevention and Treatment of
Cardiovascular Disease (https://ecqi.healthit.gov/ecqm/measures/cms347v1): Replace the current non-specified Coronary Artery Disease
measure with an e-specified measure that aligns with the Centers for
Disease Control and Prevention and the CMS Million Hearts[reg] clinical
quality measures relating to statin therapy.
Telemedicine and Virtual Visits: Collect information on
services provided via telemedicine or virtual visits by provider in
order to capture the changing health care delivery landscape.
Tenure for Health Center Staff: Retire Table 5A related to
the tenure for staff.
Workforce: Collect workforce related information,
including workforce satisfaction and health professional training.
Likely Respondents: The respondents will include Health Center
Program awardees, Health Center Program look-alikes, and NEPQR Program
awardees funded under the practice priority areas of section 831(b) of
the PHS Act.
Burden Statement: Burden includes the time expended by persons to
generate, maintain, retain, disclose or provide the information
requested. This includes the time needed to review instructions; to
develop, acquire, install, and utilize technology and systems for the
purpose of: Collecting, validating and verifying information,
processing and maintaining information, disclosing and providing
information. It also accounts for time to train personnel, respond to a
collection of information, search data sources, complete and review the
collection of information, and transmit or otherwise disclose the
information. The total annual burden hours estimated for this ICR are
summarized in the table below.
[[Page 29801]]
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of Total burden per Total burden
Form name respondents responses per responses response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Universal Report................ 1,471 1 1,471 223 328,033
Grant Report.................... 504 1 504 30 15,120
-------------------------------------------------------------------------------
Total....................... 1,975 .............. 1,975 .............. 343,153
----------------------------------------------------------------------------------------------------------------
HRSA specifically requests comments on: (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.
Amy P. McNulty,
Acting Director, Division of the Executive Secretariat.
[FR Doc. 2018-13587 Filed 6-25-18; 8:45 a.m.]
BILLING CODE 4165-15-P
