Information Collection Activities; Proposed Collection; Comment Request, 28848-28850 [2013-11340]
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28848
Federal Register / Vol. 78, No. 95 / Thursday, May 16, 2013 / Notices
Dated: May 14, 2013.
Margaret M. Shanks,
Deputy Secretary of the Board.
[FR Doc. 2013–11772 Filed 5–14–13; 11:15 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the Advisory Committee on
Blood and Tissue Safety and
Availability
Department of Health and
Human Services, Office of the Secretary,
Office of the Assistant Secretary for
Health.
ACTION: Notice.
AGENCY:
As stipulated by the Federal
Advisory Committee Act, the U.S.
Department of Health and Human
Services is hereby giving notice that the
Advisory Committee on Blood and
Tissue Safety and Availability
(ACBTSA) will hold a meeting. The
meeting will be open to the public.
DATES: The meeting will take place
Wednesday, June 5 from 8:00 a.m. to
5:00 p.m. and Thursday, June 6, 2013,
from 8:00 a.m. to 4:00 p.m.
ADDRESSES: Fishers Lane Conference
Center, Terrace Level, 5635 Fishers
Lane, Rockville, MD, 20852.
FOR FURTHER INFORMATION CONTACT: Mr.
James Berger, Designated Federal
Officer, ACBTSA, and Senior Advisor
for Blood and Tissue Safety Policy,
Office of the Assistant Secretary for
Health, Department of Health and
Human Services, 1101 Wootton
Parkway, Suite 250, Rockville, MD,
20852. Phone: (240) 453–8803; Fax (240)
453–8456; Email ACBTSA@hhs.gov.
SUPPLEMENTARY INFORMATION: The
ACBTSA shall provide advice to the
Secretary through the Assistant
Secretary for Health. The Committee
advises on a range of policy issues to
include: (1) Identification of public
health issues through surveillance of
blood, and tissue safety issues with
national biovigilance data tools; (2)
identification of public health issues
that effect availability of blood, blood
products, and tissues; (3) broad public
health, ethical and legal issues related to
the safety of blood, blood products, and
tissues; (4) the impact of various
economic factors (e.g., product cost and
supply) on safety and availability of
blood, blood products, and tissues; (5)
risk communications related to blood
transfusion and tissue transplantation;
and (6) identification of infectious
disease transmission issues for blood,
organs, blood stem cells and tissues.
tkelley on DSK3SPTVN1PROD with NOTICES
SUMMARY:
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18:13 May 15, 2013
Jkt 229001
The Advisory Committee has met
regularly since its establishment in
1997.
At the June 2013 meeting, the
ACBTSA will hear updates on recent
activities of the Department and its
agencies in support of previous
Committee recommendations.
In the past, the Committee has heard
and made recommendations regarding
policy implications related to emerging
research developments involving blood
and tissue products available for use
during public health emergencies. The
Committee noted that a nationally
coordinated system to manage tissue
supplies and distributions during a
disaster does not exist. Past
recommendations made by the ACBTSA
may be viewed at www.hhs.gov/
bloodsafety.
The focus of the meeting will be to
address whether the current blood
center system in the United States is
designed for optimal service delivery in
the era of health care reform. In
particular, the Committee hopes to
address the services currently
performed by blood centers that are
essential to the U.S. health care system,
how anticipated changes in health care
may affect blood centers and the
provision of services, as well as how the
field of transfusion medicine will be
defined in the next decade.
The public will have the opportunity
to present their views to the Committee
during a public comment session
scheduled for June 6, 2013. Comments
will be limited to five minutes per
speaker and must be pertinent to the
discussion. Pre-registration is required
for participation in the public comment
session. Any member of the public who
would like to participate in this session
is encouraged to contact the Designated
Federal Officer at his/her earliest
convenience to register for time (limited
to 5 minutes) and registration must be
prior to close of business on June 3,
2013. If it is not possible to provide 30
copies of the material to be distributed,
then individuals are requested to
provide a minimum of one (1) copy of
the document(s) to be distributed prior
to the close of business on June 3, 2013.
It is also requested that any member of
the public who wishes to provide
comments to the Committee utilizing
electronic data projection to submit the
necessary material to the Designated
Federal Officer prior to the close of
business on June 3, 2013.
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Frm 00053
Fmt 4703
Sfmt 4703
Dated: May 9, 2013.
James J. Berger,
Designated Federal Official, ACBTSA and
Senior Advisor for Blood and Tissue Safety
Policy.
[FR Doc. 2013–11582 Filed 5–15–13; 8:45 am]
BILLING CODE 4150–41–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality Agency
Information Collection Activities;
Proposed Collection; Comment
Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project:
‘‘Collection of Information for Agency
for Healthcare Research and Quality’s
(AHRQ) Hospital Survey on Patient
Safety Culture Comparative Database.’’
In accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3521,
AHRQ invites the public to comment on
this proposed information collection.
DATES: Comments on this notice must be
received by July 15, 2013.
ADDRESSES: Written comments should
be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by
email at doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection
plans, data collection instruments, and
specific details on the estimated burden
can be obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
email at doris.lefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
Proposed Project
Collection of Information for Agency
for Healthcare Research and Quality’s
(AHRQ) Hospital Survey on Patient
Safety Culture Comparative Database.
Request for information collection
approval. The Agency for Healthcare
Research and Quality (AHRQ) requests
that the Office of Management and
Budget (OMB) reapprove, under the
Paperwork Reduction Act of 1995,
AHRQ’s collection of information for
the AHRQ Hospital Survey on Patient
Safety Culture (Hospital SOPS)
Comparative Database; OMB NO. 0935–
E:\FR\FM\16MYN1.SGM
16MYN1
28849
Federal Register / Vol. 78, No. 95 / Thursday, May 16, 2013 / Notices
0162, last approved on May 5th, 2010.
The Hospital SOPS Comparative
Database consists of data from the
AHRQ Hospital Survey on Patient
Safety Culture. Hospitals in the U.S. are
asked to voluntarily submit data from
the survey to AHRQ. The database was
developed by AHRQ in 2006 in
response to requests from hospitals
interested in knowing how their patient
safety culture survey results compare to
those of other hospitals in their efforts
to improve patient safety.
Background on the Hospital SOPS. In
1999, the Institute of Medicine called
for health care organizations to develop
a ‘‘culture of safety’’ such that their
workforce and processes focus on
improving the reliability and safety of
care for patients (IOM, 1999; To Err is
Human: Building a Safer Health
System). To respond to the need for
tools to assess patient safety culture in
health care, AHRQ developed and pilot
tested the Hospital Survey on Patient
Safety Culture with OMB approval
(OMB NO. 0935–0115; Approved 2/4/
2003). The survey was designed to
enable hospitals to assess staff opinions
about patient safety issues, medical
error, and error reporting and includes
42 items that measure 12 dimensions of
patient safety culture. AHRQ released
the survey to the public along with a
Survey User’s Guide and other toolkit
materials in November 2004 on the
AHRQ Web site. Since its release, the
survey has been voluntarily used by
hundreds of hospitals in the U.S.
Rationale for the information
collection. The Hospital SOPS survey
and the Hospital SOPS Comparative
Database are supported by AHRQ to
meet its goals of promoting
improvements in the quality and safety
of health care in hospital settings. The
surveys, toolkit materials, and
comparative database results are all
made publicly available along with
technical assistance, provided by AHRQ
through its contractor at no charge to
hospitals, to facilitate the use of these
materials for hospital patient safety and
quality improvement.
This study is being conducted by
AHRQ through its contractor, Westat,
pursuant to AHRQ’s statutory authority
to conduct and support research on
healthcare and on systems for the
delivery of such care, including
activities with respect to: the quality,
effectiveness, efficiency,
appropriateness and value of healthcare
services; quality measurement and
improvement; and database
development. 42 U.S.C. 299a(a)(1), (2),
and (a)(8).
Method of Collection
All information collection for the
Hospital SOPS Comparative Database is
done electronically, except the Data Use
Agreement (DUA) that hospitals sign in
hard copy and fax or mail back.
Registration, submission of hospital
information, and data upload is handled
online through a secure Web site.
Delivery of confidential hospital survey
feedback reports is also done
electronically by having submitters
enter a username and password and
downloading their reports from a secure
Web site.
Survey data from the AHRQ Hospital
Survey on Patient Safety Culture is used
to produce three types of products: (1)
An annual Hospital SOPS Comparative
Database Report that is made publicly
available in the public domain; (2)
Individual Hospital Survey Feedback
Reports that are confidential,
customized reports produced for each
hospital that submits data to the
database; and (3) Research data sets of
individual-level and hospital-level deidentified data to enable researchers to
conduct analyses.
Estimated Annual Respondent Burden
Hospitals administer the AHRQ
Hospital Survey on Patient Safety
Culture every 20 months on average.
Therefore, the number of hospital
submissions to the database varies
because hospitals do not submit data
every year. Data submission is typically
handled by one point-of-contact (POC)
who is either a hospital patient safety
manager or a survey vendor. The POC
completes a number of data submission
steps and forms, beginning with
completion of an online Eligibility and
Registration Form. The POCs typically
submit data on behalf of 3 hospitals, on
average, because many hospitals are part
of a multi-hospital system that is
submitting data, or the POC is a vendor
that is submitting data for multiple
hospitals. Exhibits 1 and 2 are based on
an estimated 304 individual POCs who
will complete the database submission
steps and forms in the coming years, not
based on the number of ‘‘hospitals.’’ The
Hospital Information Form is completed
by all POCs for each of their hospitals.
The total annual burden hours are
estimated to be 1,793.
Exhibit 2 shows the estimated
annualized cost burden based on the
respondents’ time to submit their data.
The cost burden is estimated to be
$91,297 annually.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents/
POCs
Form name
Number of
responses per
POC
Hours per
response
Total burden
hours
Eligibility/Registration Form and Data Submission ..........................................
Data Use Agreement .......................................................................................
Hospital Information Form ...............................................................................
304
304
304
1
1
3
5.6
3/60
5/60
1,702
15
76
Total ..........................................................................................................
912
NA
NA
1,793
*The Eligibility and Registration Form requires 3 minutes to complete; however about 5.5 hours is required to prepare/plan for the data submission. This includes the amount of time POCs and other hospital staff (CEO, lawyer, database administrator) typically spend deciding whether to
participate in the database and preparing their materials and data set for submission to the database, and performing the submission.
tkelley on DSK3SPTVN1PROD with NOTICES
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents/
POCs
Form name
Eligibility/Registration Form and Data Submission ..........................................
Data Use Agreement .......................................................................................
Hospital Information Form ...............................................................................
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PO 00000
Frm 00054
Fmt 4703
Sfmt 4703
Total burden
hours
304
304
304
E:\FR\FM\16MYN1.SGM
Average hourly wage rate*
1,702
15
76
16MYN1
$50.95
50.33
50.33
Total cost
burden
$86,717
755
3,825
28850
Federal Register / Vol. 78, No. 95 / Thursday, May 16, 2013 / Notices
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN—Continued
Number of
respondents/
POCs
Form name
Total ..........................................................................................................
Total burden
hours
912
Average hourly wage rate*
1,793
NA
Total cost
burden
91,297
*Wage rates were calculated using the mean hourly wage based on occupational employment and wage estimates from the Dept of Labor, Bureau of Labor Statistics’ May 2012 National Industry-Specific Occupational Employment and Wage Estimates NAICS 622000—Hospitals, located
at https://www.bls.gov/oes/current/naics3_622000.htm. Wage rate of $50.33 is based on the mean hourly wages for Medical and Health Services
Managers (11–9111). Wage rate of $50.95 is the weighted mean hourly wage for: Medical and Health Services Managers (11–9111; $50.33 ×
2.6 hours = $130.86), Lawyers (23–1011; $72.71 × 0.5 hours 436.36), Chief Executives (11–1011($95.36 (0.5 hours = $47.68), and Database
Administrators (15–1141; $35.20 × 2 hours = $70.40) [Weighted mean = ($130.86 + 36.36 + 47.68 + 70.40)/5.6 hours = $285.3015.6 hours =
$50.95/hour].
Request for Comments
In accordance with the Paperwork
Reduction Act, comments on AHRQ’s
information collection are requested
with regard to any of the following: (a)
Whether the proposed collection of
information is necessary for the proper
performance of AHRQ health care
research and health care information
dissemination functions, including
whether the information will have
practical utility; (b) the accuracy of
AHRQ’s estimate of burden (including
hours and costs) of the proposed
collection(s) 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 upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
Dated: May 7, 2013.
Carolyn M. Clancy,
AHRQ Director.
[FR Doc. 2013–11340 Filed 5–15–13; 8:45 am]
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–7570 or send
comments to Ron Otten, 1600 Clifton
Road, MS D–74, Atlanta, GA 30333 or
send an email to omb@cdc.gov.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (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. Written comments should
be received within 60 days of this
notice.
Proposed Project
CDC Work@Health Program: Phase 1
Needs Assessment and Pilot Training
Evaluation—New—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
BILLING CODE 4160–90–M
Background and Brief Description
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–13–13SL]
tkelley on DSK3SPTVN1PROD with NOTICES
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
VerDate Mar<15>2010
18:13 May 15, 2013
Jkt 229001
In the United States, chronic diseases
such as heart disease, obesity and
diabetes are among the leading causes of
death and disability. Although chronic
diseases are among the most common
and costly health problems, they are
also among the most preventable.
Adopting healthy behaviors—such as
eating nutritious foods, being physically
active and avoiding tobacco use—can
prevent the devastating effects and
reduce the rates of these diseases.
Employers are recognizing the role
they can play in creating healthy work
environments and providing employees
with opportunities to make healthy
lifestyle choices. To support these
efforts, the Centers for Disease Control
PO 00000
Frm 00055
Fmt 4703
Sfmt 4703
and Prevention (CDC) plans to offer a
comprehensive workplace health
training program called Work@Health.
The Work@Health Program is
authorized by the Public Health Service
Act and funded through the Prevention
and Public Health Fund of the Patient
Protection and Affordable Care Act
(ACA). The Work@Health curriculum
will be based on a problem-solving
approach to improving employer
knowledge and skills related to
effective, science-based workplace
health programs, and supporting the
adoption of these programs in the
workplace. Topics to be covered in the
Work@Health curriculum include
principles, strategies, and tools for
leadership engagement; how to make a
business case for workplace health
programs; how to assess the needs of
organizations and individual
employees; how to plan, implement,
and evaluate sustainable workplace
health programs; and how to partner
with community organizations for
additional support.
The Work@Health Program will be
implemented in two phases. In Phase 1,
CDC will conduct an employer needs
assessment, develop training models,
and conduct pilot training and
evaluation with approximately 72
employers and other organizations. In
Phase 2, CDC will transition to full-scale
program implementation and evaluation
involving approximately 600 employers
and other organizations.
CDC is requesting OMB approval to
initiate Phase 1 information collection
in summer 2013. A one-time Training
Needs Assessment Survey will be
administered electronically to 200
employers representing small, mid-size,
and large businesses from various
industry sectors and geographic locales.
The needs assessment survey will allow
CDC to assess employer preferences
with respect to curriculum content, the
types of support materials needed by
employers and the appropriate level of
detail for these materials, and the best
approaches for providing technical
assistance to employers. The estimated
E:\FR\FM\16MYN1.SGM
16MYN1
Agencies
[Federal Register Volume 78, Number 95 (Thursday, May 16, 2013)]
[Notices]
[Pages 28848-28850]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-11340]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality Agency
Information Collection Activities; Proposed Collection; Comment
Request
AGENCY: Agency for Healthcare Research and Quality, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the intention of the Agency for
Healthcare Research and Quality (AHRQ) to request that the Office of
Management and Budget (OMB) approve the proposed information collection
project: ``Collection of Information for Agency for Healthcare Research
and Quality's (AHRQ) Hospital Survey on Patient Safety Culture
Comparative Database.'' In accordance with the Paperwork Reduction Act,
44 U.S.C. 3501-3521, AHRQ invites the public to comment on this
proposed information collection.
DATES: Comments on this notice must be received by July 15, 2013.
ADDRESSES: Written comments should be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by email at
doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection plans, data collection
instruments, and specific details on the estimated burden can be
obtained from the AHRQ Reports Clearance Officer.
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427-1477, or by email at
doris.lefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
Collection of Information for Agency for Healthcare Research and
Quality's (AHRQ) Hospital Survey on Patient Safety Culture Comparative
Database.
Request for information collection approval. The Agency for
Healthcare Research and Quality (AHRQ) requests that the Office of
Management and Budget (OMB) reapprove, under the Paperwork Reduction
Act of 1995, AHRQ's collection of information for the AHRQ Hospital
Survey on Patient Safety Culture (Hospital SOPS) Comparative Database;
OMB NO. 0935-
[[Page 28849]]
0162, last approved on May 5th, 2010. The Hospital SOPS Comparative
Database consists of data from the AHRQ Hospital Survey on Patient
Safety Culture. Hospitals in the U.S. are asked to voluntarily submit
data from the survey to AHRQ. The database was developed by AHRQ in
2006 in response to requests from hospitals interested in knowing how
their patient safety culture survey results compare to those of other
hospitals in their efforts to improve patient safety.
Background on the Hospital SOPS. In 1999, the Institute of Medicine
called for health care organizations to develop a ``culture of safety''
such that their workforce and processes focus on improving the
reliability and safety of care for patients (IOM, 1999; To Err is
Human: Building a Safer Health System). To respond to the need for
tools to assess patient safety culture in health care, AHRQ developed
and pilot tested the Hospital Survey on Patient Safety Culture with OMB
approval (OMB NO. 0935-0115; Approved 2/4/2003). The survey was
designed to enable hospitals to assess staff opinions about patient
safety issues, medical error, and error reporting and includes 42 items
that measure 12 dimensions of patient safety culture. AHRQ released the
survey to the public along with a Survey User's Guide and other toolkit
materials in November 2004 on the AHRQ Web site. Since its release, the
survey has been voluntarily used by hundreds of hospitals in the U.S.
Rationale for the information collection. The Hospital SOPS survey
and the Hospital SOPS Comparative Database are supported by AHRQ to
meet its goals of promoting improvements in the quality and safety of
health care in hospital settings. The surveys, toolkit materials, and
comparative database results are all made publicly available along with
technical assistance, provided by AHRQ through its contractor at no
charge to hospitals, to facilitate the use of these materials for
hospital patient safety and quality improvement.
This study is being conducted by AHRQ through its contractor,
Westat, pursuant to AHRQ's statutory authority to conduct and support
research on healthcare and on systems for the delivery of such care,
including activities with respect to: the quality, effectiveness,
efficiency, appropriateness and value of healthcare services; quality
measurement and improvement; and database development. 42 U.S.C.
299a(a)(1), (2), and (a)(8).
Method of Collection
All information collection for the Hospital SOPS Comparative
Database is done electronically, except the Data Use Agreement (DUA)
that hospitals sign in hard copy and fax or mail back. Registration,
submission of hospital information, and data upload is handled online
through a secure Web site. Delivery of confidential hospital survey
feedback reports is also done electronically by having submitters enter
a username and password and downloading their reports from a secure Web
site.
Survey data from the AHRQ Hospital Survey on Patient Safety Culture
is used to produce three types of products: (1) An annual Hospital SOPS
Comparative Database Report that is made publicly available in the
public domain; (2) Individual Hospital Survey Feedback Reports that are
confidential, customized reports produced for each hospital that
submits data to the database; and (3) Research data sets of individual-
level and hospital-level de-identified data to enable researchers to
conduct analyses.
Estimated Annual Respondent Burden
Hospitals administer the AHRQ Hospital Survey on Patient Safety
Culture every 20 months on average. Therefore, the number of hospital
submissions to the database varies because hospitals do not submit data
every year. Data submission is typically handled by one point-of-
contact (POC) who is either a hospital patient safety manager or a
survey vendor. The POC completes a number of data submission steps and
forms, beginning with completion of an online Eligibility and
Registration Form. The POCs typically submit data on behalf of 3
hospitals, on average, because many hospitals are part of a multi-
hospital system that is submitting data, or the POC is a vendor that is
submitting data for multiple hospitals. Exhibits 1 and 2 are based on
an estimated 304 individual POCs who will complete the database
submission steps and forms in the coming years, not based on the number
of ``hospitals.'' The Hospital Information Form is completed by all
POCs for each of their hospitals. The total annual burden hours are
estimated to be 1,793.
Exhibit 2 shows the estimated annualized cost burden based on the
respondents' time to submit their data. The cost burden is estimated to
be $91,297 annually.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Number of
Form name respondents/ responses per Hours per Total burden
POCs POC response hours
----------------------------------------------------------------------------------------------------------------
Eligibility/Registration Form and Data 304 1 5.6 1,702
Submission.....................................
Data Use Agreement.............................. 304 1 3/60 15
Hospital Information Form....................... 304 3 5/60 76
---------------------------------------------------------------
Total....................................... 912 NA NA 1,793
----------------------------------------------------------------------------------------------------------------
*The Eligibility and Registration Form requires 3 minutes to complete; however about 5.5 hours is required to
prepare/plan for the data submission. This includes the amount of time POCs and other hospital staff (CEO,
lawyer, database administrator) typically spend deciding whether to participate in the database and preparing
their materials and data set for submission to the database, and performing the submission.
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Number of
Form name respondents/ Total burden Average hourly Total cost
POCs hours wage rate* burden
----------------------------------------------------------------------------------------------------------------
Eligibility/Registration Form and Data 304 1,702 $50.95 $86,717
Submission.....................................
Data Use Agreement.............................. 304 15 50.33 755
Hospital Information Form....................... 304 76 50.33 3,825
---------------------------------------------------------------
[[Page 28850]]
Total....................................... 912 1,793 NA 91,297
----------------------------------------------------------------------------------------------------------------
*Wage rates were calculated using the mean hourly wage based on occupational employment and wage estimates from
the Dept of Labor, Bureau of Labor Statistics' May 2012 National Industry-Specific Occupational Employment and
Wage Estimates NAICS 622000--Hospitals, located at https://www.bls.gov/oes/current/naics3_622000.htm. Wage
rate of $50.33 is based on the mean hourly wages for Medical and Health Services Managers (11-9111). Wage rate
of $50.95 is the weighted mean hourly wage for: Medical and Health Services Managers (11-9111; $50.33 x 2.6
hours = $130.86), Lawyers (23-1011; $72.71 x 0.5 hours 436.36), Chief Executives (11-1011($95.36 (0.5 hours =
$47.68), and Database Administrators (15-1141; $35.20 x 2 hours = $70.40) [Weighted mean = ($130.86 + 36.36 +
47.68 + 70.40)/5.6 hours = $285.3015.6 hours = $50.95/hour].
Request for Comments
In accordance with the Paperwork Reduction Act, comments on AHRQ's
information collection are requested with regard to any of the
following: (a) Whether the proposed collection of information is
necessary for the proper performance of AHRQ health care research and
health care information dissemination functions, including whether the
information will have practical utility; (b) the accuracy of AHRQ's
estimate of burden (including hours and costs) of the proposed
collection(s) 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 upon the
respondents, including the use of automated collection techniques or
other forms of information technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
proposed information collection. All comments will become a matter of
public record.
Dated: May 7, 2013.
Carolyn M. Clancy,
AHRQ Director.
[FR Doc. 2013-11340 Filed 5-15-13; 8:45 am]
BILLING CODE 4160-90-M