Agency Forms Undergoing Paperwork Reduction Act Review, 20601-20602 [2010-9086]
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20601
Federal Register / Vol. 75, No. 75 / Tuesday, April 20, 2010 / Notices
ESTIMATE OF ANNUALIZED BURDEN TABLE—Continued
Number of
respondents
Types of data collection
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Screener—Site B .............................................................................................
Locator—Site B ................................................................................................
Baseline Assessment—Site B .........................................................................
Follow-up Assessment—Site B .......................................................................
Screener—Site C .............................................................................................
Locator—Site C ...............................................................................................
Baseline Assessment—Site C .........................................................................
Follow-up Assessment—Site C .......................................................................
214
80
80
80
200
80
80
80
1
1
1
1
1
1
1
1
10/60
5/60
45/60
45/60
5/60
5/60
20/60
20/60
36
7
60
60
17
7
27
27
Total ..........................................................................................................
........................
........................
........................
335
Dated: April 14, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2010–9087 Filed 4–19–10; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–10–09CK]
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 20503 or by fax to (202) 395–5806.
Written comments should be received
within 30 days of this notice.
Proposed Project
Asthma Information Reporting System
(AIRS)—New—Air Pollution and
Respiratory Health Branch (APRHB),
National Center for Environmental
Health (NCEH), Centers for Disease
Control and Prevention (CDC).
erowe on DSK5CLS3C1PROD with NOTICES
Background and Brief Description
In 1999, the CDC began developing its
National Asthma Control Program, a
population-based, public health
approach to addressing the burden of
asthma. The program supports the goals
and objectives of ‘‘Healthy People 2010’’
for asthma and is based on the public
health principles of surveillance,
VerDate Nov<24>2008
14:55 Apr 19, 2010
Jkt 220001
partnerships, and interventions. This
data collection request will provide
NCEH with routine information,
through a semi-annual Management
Information System, AIRS, about the
activities and performance of the State
and territorial grantees funded under
the National Asthma Control Program.
The primary purpose of the National
Asthma Control Program is to develop
program capacity to address asthma
from a public health perspective to
bring about: (1) A focus on asthmarelated activity within States; (2) an
increased understanding of asthmarelated data and its application to
program planning and evaluation
through the development and
maintenance of an ongoing asthma
surveillance system; (3) an increased
recognition, within the public health
structure of States, of the potential to
use a public health approach to reduce
the burden of asthma; (4) linkages of
State health agencies to other agencies
and organizations addressing asthma in
the population; and (5) implementation
of interventions to achieve positive
health impacts, such as reducing the
number of deaths, hospitalizations,
emergency department visits, school or
work days missed, and limitations on
activity due to asthma.
The proposed AIRS management
information system will be comprised of
multiple components that enable the
electronic reporting of three types of
data/information from State asthma
control programs: (1) Information that is
currently collected as part of interim
(semi-annual) and end-of-year progress
reporting, (2) Aggregate level reports of
surveillance data on long-term program
outcomes, and (3) Specific data
indicative of progress made on:
Partnerships, surveillance,
interventions, and evaluation.
Currently, data is collected on an
interim (semi-annual) basis from State
asthma control programs as part of
regular reporting of cooperative
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
agreement activities. Programs report
information such as progress to date on
accomplishing intended objectives,
programmatic changes, changes to
staffing or management, and budgetary
information. Regular reporting of this
information is a requirement of the cooperative agreement mechanism utilized
to fund State asthma control programs.
Information in this section will be
consistent with previous reporting by
States through Grants.gov. States will be
required to submit interim (semiannual) and year-end progress report
information into AIRS, thus this type of
programmatic information on activities
and objectives will be collected twice
per year (interim report and end-of-year
report).
The National Asthma Control Program
at CDC has access to and analyzes
national-level asthma surveillance data
(https://www.cdc.gov/asthma/
asthmadata.htm). With the exception of
data from the Behavioral Risk Factor
Surveillance System (BRFSS), analyses
cannot be conducted at the level of the
State. Therefore, as part of AIRS, State
asthma control programs will be asked
to submit aggregate surveillance data to
allow calculation of State asthma
surveillance indicators across all funded
States (where data is available) in a
standardized manner. Data likely to be
requested through this system include:
Hospital discharges (with asthma as first
listed diagnosis), and emergency
department visits (with asthma as first
listed diagnosis). States will be required
to submit this information into AIRS
once per year, in conjunction with the
end of year reporting of activities and
objectives described above.
National and State asthma
surveillance data provide information
useful to examining progress on longterm outcomes of State asthma
programs. To identify appropriate
indicators of program implementation
and short-term outcomes, CDC
convened and facilitated workgroups
E:\FR\FM\20APN1.SGM
20APN1
20602
Federal Register / Vol. 75, No. 75 / Tuesday, April 20, 2010 / Notices
comprised of State asthma control
program representatives over the course
of two years. In collaboration with these
workgroups, the CDC generated specific
questions (qualitative and quantitative
in nature) intended to collect data on
key features of State asthma control
programs:
environment about what is working in
State asthma programs and to identify
potential areas for improvement. There
are no costs to respondents, other than
their time. The total estimated annual
burden hours are 288.
Partnerships, surveillance,
interventions, and evaluation. States
will be asked to provide answers to
these questions once per year in
conjunction with the end of year
reporting of activities and objectives,
described above. These data will be
used to foster a continuous learning
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Forms
Number of
respondents
Number of
response per
respondent
Burden per
response
(in hours)
State Health Departments ..............................
Interim and end of year reports on activities
and objectives.
36
2
4
Dated: April 14, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2010–9086 Filed 4–19–10; 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, e-mail
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: The Stem Cell
Therapeutic Outcomes Database (OMB
No. 0915–0310)—Extension
The Stem Cell Therapeutic and
Research Act of 2005 provides for the
collection and maintenance of human
cord blood stem cells for the treatment
of patients and research. The Health
Resources and Services
Number of
respondents
Reporting
Responses
per
respondent
Administration’s (HRSA) Healthcare
Systems Bureau (HSB) has established
the Stem Cell Therapeutic Outcomes
Database. Operation of this database
necessitates certain recordkeeping and
reporting requirements in order to
perform the functions related to
hematopoietic stem cell transplantation
under contract to HHS. The Act requires
the Secretary to contract for the
establishment and maintenance of
information related to patients who
have received stem cell therapeutic
products and to do so using a
standardized, electronic format. Data is
collected from transplant centers in a
manner similar to the data collection
activities conducted by the Center for
International Blood and Marrow
Transplant Research (CIBMTR) and is
used for ongoing analysis of transplant
outcomes. HRSA uses the information
in order to carry out its statutory
responsibilities. Information is needed
to monitor the clinical status of
transplantation and to provide the
Secretary with an annual report of
transplant center-specific survival data.
The estimate of burden is as follows:
Total
responses
Hours per
response
250
250
250
250
250
250
250
40
40
40
28
22
40
25
8,000
8,000
8,000
5,538
4,308
8,000
4,923
2.25
1
2.25
2.25
2.25
2.25
0.5
Total ..........................................................................
erowe on DSK5CLS3C1PROD with NOTICES
Baseline Patient/Day of Transplant Data ........................
Product Receipt/Analysis/Preparation Data .....................
100-Day Post-Transplant Data ........................................
6-Month Post-Transplant Data .........................................
12-Month Post-Transplant Data .......................................
Annual Post-Transplant Data (year two and beyond) .....
Death Information ............................................................
250
........................
46,769
..........................
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14:55 Apr 19, 2010
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PO 00000
Frm 00048
Fmt 4703
Sfmt 4703
E:\FR\FM\20APN1.SGM
20APN1
Total burden
hours
18,000
8,000
18,000
12,460.5
9,693
18,000
2,461.5
86,615
]]>Agencies
[Federal Register Volume 75, Number 75 (Tuesday, April 20, 2010)]
[Notices]
[Pages 20601-20602]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-9086]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-10-09CK]
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 e-mail
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
Asthma Information Reporting System (AIRS)--New--Air Pollution and
Respiratory Health Branch (APRHB), National Center for Environmental
Health (NCEH), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
In 1999, the CDC began developing its National Asthma Control
Program, a population-based, public health approach to addressing the
burden of asthma. The program supports the goals and objectives of
``Healthy People 2010'' for asthma and is based on the public health
principles of surveillance, partnerships, and interventions. This data
collection request will provide NCEH with routine information, through
a semi-annual Management Information System, AIRS, about the activities
and performance of the State and territorial grantees funded under the
National Asthma Control Program.
The primary purpose of the National Asthma Control Program is to
develop program capacity to address asthma from a public health
perspective to bring about: (1) A focus on asthma-related activity
within States; (2) an increased understanding of asthma-related data
and its application to program planning and evaluation through the
development and maintenance of an ongoing asthma surveillance system;
(3) an increased recognition, within the public health structure of
States, of the potential to use a public health approach to reduce the
burden of asthma; (4) linkages of State health agencies to other
agencies and organizations addressing asthma in the population; and (5)
implementation of interventions to achieve positive health impacts,
such as reducing the number of deaths, hospitalizations, emergency
department visits, school or work days missed, and limitations on
activity due to asthma.
The proposed AIRS management information system will be comprised
of multiple components that enable the electronic reporting of three
types of data/information from State asthma control programs: (1)
Information that is currently collected as part of interim (semi-
annual) and end-of-year progress reporting, (2) Aggregate level reports
of surveillance data on long-term program outcomes, and (3) Specific
data indicative of progress made on: Partnerships, surveillance,
interventions, and evaluation.
Currently, data is collected on an interim (semi-annual) basis from
State asthma control programs as part of regular reporting of
cooperative agreement activities. Programs report information such as
progress to date on accomplishing intended objectives, programmatic
changes, changes to staffing or management, and budgetary information.
Regular reporting of this information is a requirement of the co-
operative agreement mechanism utilized to fund State asthma control
programs. Information in this section will be consistent with previous
reporting by States through Grants.gov. States will be required to
submit interim (semi-annual) and year-end progress report information
into AIRS, thus this type of programmatic information on activities and
objectives will be collected twice per year (interim report and end-of-
year report).
The National Asthma Control Program at CDC has access to and
analyzes national-level asthma surveillance data (https://www.cdc.gov/asthma/asthmadata.htm). With the exception of data from the Behavioral
Risk Factor Surveillance System (BRFSS), analyses cannot be conducted
at the level of the State. Therefore, as part of AIRS, State asthma
control programs will be asked to submit aggregate surveillance data to
allow calculation of State asthma surveillance indicators across all
funded States (where data is available) in a standardized manner. Data
likely to be requested through this system include: Hospital discharges
(with asthma as first listed diagnosis), and emergency department
visits (with asthma as first listed diagnosis). States will be required
to submit this information into AIRS once per year, in conjunction with
the end of year reporting of activities and objectives described above.
National and State asthma surveillance data provide information
useful to examining progress on long-term outcomes of State asthma
programs. To identify appropriate indicators of program implementation
and short-term outcomes, CDC convened and facilitated workgroups
[[Page 20602]]
comprised of State asthma control program representatives over the
course of two years. In collaboration with these workgroups, the CDC
generated specific questions (qualitative and quantitative in nature)
intended to collect data on key features of State asthma control
programs:
Partnerships, surveillance, interventions, and evaluation. States
will be asked to provide answers to these questions once per year in
conjunction with the end of year reporting of activities and
objectives, described above. These data will be used to foster a
continuous learning environment about what is working in State asthma
programs and to identify potential areas for improvement. There are no
costs to respondents, other than their time. The total estimated annual
burden hours are 288.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Burden per
Type of respondent Forms Number of response per response (in
respondents respondent hours)
----------------------------------------------------------------------------------------------------------------
State Health Departments............ Interim and end of year 36 2 4
reports on activities
and objectives.
----------------------------------------------------------------------------------------------------------------
Dated: April 14, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2010-9086 Filed 4-19-10; 8:45 am]
BILLING CODE 4163-18-P
