Agency Forms Undergoing Paperwork Reduction Act Review, 58394-58395 [2010-24016]
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58394
Federal Register / Vol. 75, No. 185 / Friday, September 24, 2010 / Notices
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC 20503 or by fax to (202) 395–5806.
Written comments should be received
within 30 days of this notice.
Proposed Project
Application Form and Related Forms
for the Operation of the National Death
Index, (OMB No. 0920–0215, Expiration
12/31/2010)—Extension—National
Center for Health Statistics (NCHS),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C.), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on the extent and nature of
illness and disability of the population
of the United States.
The National Death Index (NDI) is a
national data base containing
identifying death record information
submitted annually to NCHS by all the
state vital statistics offices, beginning
with deaths in 1979. Searches against
the NDI file provide the states and dates
of death, and the death certificate
numbers of deceased study subjects.
Using the NDI Plus service,
researchers have the option of also
receiving cause of death information for
deceased subjects, thus reducing the
need to request copies of death
certificates from the states. The NDI
Plus option currently provides the
International Classification of Disease
(ICD) codes for the underlying and
multiple causes of death for the years
1979–2007. Health researchers must
complete administrative forms in order
to apply for NDI services, and submit
records of study subjects for computer
matching against the NDI file. A threeyear clearance is requested. There is no
cost to respondents except for their
time. The total estimated annual burden
hours are 182.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response (in
hours)
Type of respondents
Form name
Health Researchers in Government, Universities,
and Private Industry.
Health Researchers in Government, Universities,
and Private Industry.
Health Researchers in Government, Universities,
and Private Industry.
Application Form ....................................
50
1
2.5
Repeat Request Form ...........................
70
1
18/60
Data Transmittal Form ...........................
120
1
18/60
Dated: September 20, 2010.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2010–24017 Filed 9–23–10; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–10–0743]
srobinson on DSKHWCL6B1PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
VerDate Mar<15>2010
16:12 Sep 23, 2010
Jkt 220001
Proposed Project
Assessment and Monitoring of
Breastfeeding-Related Maternity Care
Practices in Intra-partum Care Facilities
in the United States and Territories
(OMB Control No. 0920–0743, Exp. 10/
31/2010)—Revision—National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
Substantial evidence demonstrates the
health benefits of breastfeeding.
Breastfeeding mothers have lower risks
of breast and ovarian cancers and type
2 diabetes, and breastfeeding better
protects infants against infections,
chronic diseases like diabetes and
obesity, and even childhood leukemia
and sudden infant death syndrome
(SIDS). However, the groups that are at
higher risk for diabetes, obesity, and
poor health overall persistently have the
lowest breastfeeding rates. Public health
priorities for the U.S. include increasing
the overall rate of breastfeeding, and
reducing variation in breastfeeding rates
across population subgroups.
The health care system is one of the
most important and effective settings to
improve breastfeeding. In 2007, CDC
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conducted the first national survey of
Maternity Practices in Infant Nutrition
and Care (known as the mPINC Survey)
in health care facilities (hospitals and
free-standing childbirth centers) to
provide baseline information. The
survey was designed to provide baseline
information and to be repeated again
every two years. The second iteration of
the survey was conducted in 2009. The
survey inquired about patient education
and support for breastfeeding
throughout the maternity stay as well as
staff training and maternity care
policies. Each responding organization
received a customized Benchmark
Report as well as other feedback to use
in self-assessment and quality
improvement activities.
CDC proposes to repeat the mPINC in
2011 using previously fielded questions
and methodology. In addition to all
facilities that participated in 2007 or
2009, the 2011 survey will include those
that were invited but did not participate
in 2007 or 2009 and any that are new
since then. All birth centers and
hospitals with ≥1 registered maternity
bed will be screened via a brief phone
call to assess their eligibility, identify
additional locations, and identify the
appropriate point of contact.
E:\FR\FM\24SEN1.SGM
24SEN1
58395
Federal Register / Vol. 75, No. 185 / Friday, September 24, 2010 / Notices
A major goal of the 2011 survey is to
be fully responsive to respondents’
needs for information and technical
assistance. CDC will again provide
customized benchmark reports to
respondents and document progress
since 2009 on their quality
improvement efforts. National and state
reports will use de-identified data to
describe incremental changes in
practices and care processes over time at
the facility, state, and national levels.
Participation in the survey is
voluntary, and responses may be
submitted by mail or through a webbased system. There are no costs to
respondents other than their time. The
total estimated annualized burden hours
are 1,686.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Form name
Number of
respondents
Number of
responses per
respondent
Average burden
per response
(in hours)
Hospitals ...................................................
Telephone Screening Interview for Hospitals.
2011 mPINC Survey for Hospitals ...........
Telephone Screening Interview for Birth
Centers.
2011 mPINC Survey for Birth Centers .....
3,897
1
5/60
2,568
192
1
1
30/60
5/60
122
1
30/60
Birth Centers .............................................
Dated: September 17, 2010.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2010–24016 Filed 9–23–10; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection:
Comment Request
In compliance with the requirement
for opportunity for public comment on
proposed data collection projects
(section 3506(c)(2)(A) of Title 44, United
States Code, as amended by the
Paperwork Reduction Act of 1995, Pub.
L. 104–13), the Health Resources and
Services Administration (HRSA)
publishes periodic summaries of
proposed projects being developed for
submission to the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995. 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 the HRSA
Reports Clearance Officer at (301) 443–
1129.
Comments are invited on: (a) The
proposed collection of information for
the proper performance of the functions
of the Agency; (b) the accuracy of the
Agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology.
Proposed Project: Health Center
Controlled Networks Progress Reports
(OMB No. 0915–0315)—Revision
The Health Resources and Services
Administration (HRSA) collects network
outcome measures, conducts evaluation
of those measures, and has an electronic
reporting system for the following types
of grantees: Health Information
Technology Planning Grants, Electronic
Health Record Implementation Health
Number of
respondents
srobinson on DSKHWCL6B1PROD with NOTICES
Application
Responses
per
respondent
Center Controlled Networks, Health
Information Technology Innovations for
Health Center Controlled Networks, and
High Impact Electronic Health Records
Implementation for Health Center
Controlled Networks and Large Multi
Site Health Centers. In order to help
carry out its mission, HRSA created a
set of performance measures that
grantees use to evaluate the
effectiveness of their service programs
and monitor their progress through the
use of performance reporting data.
Grantees report to HRSA on their
grants to accomplish the following
goals: increase access to needed data
and services; improve quality, efficiency
and effectiveness of network services;
and enhance ability to track and
monitor patient outcomes. Grantees
submit their Progress Reports in a midyear report and an accumulative annual
progress report each fiscal year of the
grant. These grants are on three year
project periods. For HRSA grantees,
there is no increase in burden. The
hours per response has not changed.
The number of grantees increased from
40 to 109.
The annual estimate of burden is as
follows:
Total
responses
Hours per
response
Total burden
hours
Planning ...............................................................................
Electronic Health Records Implementation .........................
Innovations Category 1 ........................................................
Innovations Category 2 ........................................................
High Impact ..........................................................................
5
54
0
29
21
2
2
2
2
2
10
108
0
58
42
10
18
0
18
18
100
1,944
0
1,044
7,208
Total ..............................................................................
109
-
80
-
3,808
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]]>Agencies
[Federal Register Volume 75, Number 185 (Friday, September 24, 2010)]
[Notices]
[Pages 58394-58395]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-24016]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-10-0743]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-5960 or send an email to
omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-5806.
Written comments should be received within 30 days of this notice.
Proposed Project
Assessment and Monitoring of Breastfeeding-Related Maternity Care
Practices in Intra-partum Care Facilities in the United States and
Territories (OMB Control No. 0920-0743, Exp. 10/31/2010)--Revision--
National Center for Chronic Disease Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Substantial evidence demonstrates the health benefits of
breastfeeding. Breastfeeding mothers have lower risks of breast and
ovarian cancers and type 2 diabetes, and breastfeeding better protects
infants against infections, chronic diseases like diabetes and obesity,
and even childhood leukemia and sudden infant death syndrome (SIDS).
However, the groups that are at higher risk for diabetes, obesity, and
poor health overall persistently have the lowest breastfeeding rates.
Public health priorities for the U.S. include increasing the overall
rate of breastfeeding, and reducing variation in breastfeeding rates
across population subgroups.
The health care system is one of the most important and effective
settings to improve breastfeeding. In 2007, CDC conducted the first
national survey of Maternity Practices in Infant Nutrition and Care
(known as the mPINC Survey) in health care facilities (hospitals and
free-standing childbirth centers) to provide baseline information. The
survey was designed to provide baseline information and to be repeated
again every two years. The second iteration of the survey was conducted
in 2009. The survey inquired about patient education and support for
breastfeeding throughout the maternity stay as well as staff training
and maternity care policies. Each responding organization received a
customized Benchmark Report as well as other feedback to use in self-
assessment and quality improvement activities.
CDC proposes to repeat the mPINC in 2011 using previously fielded
questions and methodology. In addition to all facilities that
participated in 2007 or 2009, the 2011 survey will include those that
were invited but did not participate in 2007 or 2009 and any that are
new since then. All birth centers and hospitals with >=1 registered
maternity bed will be screened via a brief phone call to assess their
eligibility, identify additional locations, and identify the
appropriate point of contact.
[[Page 58395]]
A major goal of the 2011 survey is to be fully responsive to
respondents' needs for information and technical assistance. CDC will
again provide customized benchmark reports to respondents and document
progress since 2009 on their quality improvement efforts. National and
state reports will use de-identified data to describe incremental
changes in practices and care processes over time at the facility,
state, and national levels.
Participation in the survey is voluntary, and responses may be
submitted by mail or through a web-based system. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 1,686.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response (in
respondents respondent hours)
----------------------------------------------------------------------------------------------------------------
Hospitals........................ Telephone Screening 3,897 1 5/60
Interview for
Hospitals.
2011 mPINC Survey 2,568 1 30/60
for Hospitals.
Birth Centers.................... Telephone Screening 192 1 5/60
Interview for Birth
Centers.
2011 mPINC Survey 122 1 30/60
for Birth Centers.
----------------------------------------------------------------------------------------------------------------
Dated: September 17, 2010.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2010-24016 Filed 9-23-10; 8:45 am]
BILLING CODE 4163-18-P
