Agency Information Collection Activities: Proposed Collection; Comment Request, 43238-43239 [E8-16874]
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43238
Federal Register / Vol. 73, No. 143 / Thursday, July 24, 2008 / Notices
Terry Nicolosi,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. E8–16963 Filed 7–23–08; 8:45 am]
BILLING CODE 4150–31–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.
AGENCY:
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:
‘‘National Study of the Hospital Adverse
Event Reporting Follow-Up Survey.’’ In
accordance with the Paperwork
Reduction Act of 1995, 44 U.S.C.
3506(c)(2)(A), AHRQ invites the public
to comment on this proposed
information collection.
Comments on this notice must be
received by September 22, 2008.
DATES:
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.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
e-mail at doris.lefkowitz@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
‘‘National Study of the Hospital Adverse
Event Reporting Follow-Up Survey’’
This proposed information collection
will conduct a survey similar to a
previous AHRQ baseline survey
conducted in 2005, which examined
and characterized adverse event
reporting in the Nation’s hospitals
(Farley DO, Haviland A, Champagne S,
Jam AK, Battles JB, Munier WB, Loeb
JM. Adverse Event Reporting Practices
by U.S. Hospitals: Results of a National
Survey, under review for publication).
The follow-up survey will allow AHRQ
to examine how hospitals’ use of
adverse event reporting systems has
changed over time. The baseline survey
was completed by 1,652 hospital risk
managers selected from a nationally
representative sample frame. The
follow-up survey will consist of a
random sample of 1,200 of the
respondents to the baseline survey. We
anticipate an 85% response rate for the
follow-up survey, resulting in 1,020
completed questionnaires.
Similar to the baseline survey, the
follow-up survey will ascertain whether
hospitals collect information on adverse
events, and how the information is
stored. Information will also be
collected regarding the hospital’s case
definition of a reportable event, whether
information on the severity of the
adverse event is collected, who might
report this information and whether
they can report to a system which is
confidential and/or anonymous. The
questionnaire also asks about the uses of
the data that are collected, and whether
information is used for purposes
including analytic uses, personnel
action, and improvement interventions.
Finally, the questionnaire asks about the
other sources of information that are
useful to hospitals for patient safetyrelated interventions.
This project is being conducted
pursuant to AHRQ’s statutory mandates
to (1) promote health care quality
improvement by conducting and
supporting research that develops and
presents scientific evidence regarding
all aspects of health care, including
methods for measuring quality and
strategies for improving quality (42
U.S.C. 299(b)(1)(F)) and (2) conduct and
support research on health care and on
systems for the delivery of such care,
including activities with respect to
quality measurement and improvement
(42 U.S.C. 299a(a)(2)). In addition,
Congress has, in report language,
directed AHRQ to provide a report
detailing the results of its efforts to
reduce medical errors. See Report for
the Departments of Labor, Health and
Human Services, and Education, and
related agencies Appropriation Bill for
Fiscal Year 2002, S. Rep. 107–84, at 11
(2001).
This project is being funded by AHRQ
and conducted by the RAND
corporation as part of a contract under
which RAND serves as the Patient
Safety Evaluation center for AHRQ’s
patient safety initiative.
Method of Collection
The baseline survey and data
collection procedures have been
previously conducted and reviewed
(under OMB Number 0935–0125,
Expiration Date 07/31/2008). The
follow-up survey will include an initial
mailed survey with two waves of mailed
follow-ups as needed, and a computerAssisted Telephone Interviewing (CATI)
survey follow-up for the remaining nonresponders. The survey will be
completed by one Risk Manager per
hospital.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated
annualized burden hours for the
respondents’ time to participate in this
information collection. The
questionnaire is expected to require 25
minutes to complete, resulting in a total
burden of 425 hours.
Exhibit 2 shows the estimated
annualized cost burden for the
respondents, which is estimated to be
$11,518. The respondents will not incur
any other costs beyond those associated
with their time to participate.
EXHIBIT 1.—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Hours per
response
Total burden
hours
ebenthall on PRODPC60 with NOTICES
Risk manager questionnaire ............................................................................
1,020
1
25/60
425
Total ..........................................................................................................
1,020
NA
NA
425
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43239
Federal Register / Vol. 73, No. 143 / Thursday, July 24, 2008 / Notices
EXHIBIT 2.—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents
Form name
Total burden
hours
Average hourly wage rate*
Total cost
burden
Risk manager questionnaire ............................................................................
1,020
425
$27.10
$11,518
Total ..........................................................................................................
1,020
425
NA
11,518
* Based upon the mean of the average wages, National Compensation Survey: Occupational wages in the United States 2006, ‘‘U.S. Department of Labor, Bureau of Labor Statistics.’’
Estimated Annual Costs to the Federal
Government
The Agency is supporting the conduct
of this survey and analysis of survey
data as part of a contract with the RAND
Corporation under which RAND serves
as the Patient Safety Evaluation Center
for AHRQ’s patient safety initiative. The
estimated cost for this work is $240,000,
including $190,000 for data collection
activities and $50,000 to design the
study, analyze the data and report the
findings.
Request for Comments
In accordance with the above-cited
Paperwork Reduction Act legislation,
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, quality
improvement and 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: July 16, 2008.
Carolyn M. Clancy,
Director.
[FR Doc. E8–16874 Filed 7–23–08; 8:45 am]
BILLING CODE 4160–90–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30 Day–08–0706]
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) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
National Program of Cancer Registries
Program Evaluation Instrument (NPCR–
PEI)—Revision—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC is responsible for administering
and monitoring the National Program of
Cancer Registries (NPCR). As of 2008,
CDC supports 45 states, two territories,
the District of Columbia, and the Pacific
Island Jurisdictions’ unified Central
Cancer Registry (CCR) for populationbased cancer registries. CCRs are the
foundation of cancer prevention and
control, providing information from
reporting jurisdictions to ensure that
high-quality and timely cancer
surveillance data are available to CDC.
CDC has collected program activity
information from NPCR-funded
registries on an annual basis. Beginning
in 2009, CDC proposes to change the
data collection frequency from annual to
every other year, with data collection
occurring only in odd-numbered years.
Information will be collected
electronically in 2009 and 2011 using
the Web-based Program Evaluation
Instrument (NPCR–PEI). The
information will be used to evaluate
various attributes of the registries
funded by NPCR, monitor NPCR
registries’ progress towards program
standards and objectives, compare an
individual NPCR registry’s progress
towards standards with national
program standards, and disseminate
information about the NPCR. Continued
clearance for a three-year period is
requested.
There are no costs to respondents
except their time. The total estimated
annualized burden hours are 50.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses
per respondent
Average
burden
per response
(in hours)
NPCR Grantees ...........................................................................................................................
ebenthall on PRODPC60 with NOTICES
Type of respondents
33
1
1.5
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Agencies
[Federal Register Volume 73, Number 143 (Thursday, July 24, 2008)]
[Notices]
[Pages 43238-43239]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-16874]
-----------------------------------------------------------------------
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: ``National Study of the Hospital Adverse Event Reporting
Follow-Up Survey.'' In accordance with the Paperwork Reduction Act of
1995, 44 U.S.C. 3506(c)(2)(A), AHRQ invites the public to comment on
this proposed information collection.
DATES: Comments on this notice must be received by September 22, 2008.
ADDRESSES: Written comments should be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by e-mail 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 e-mail at
doris.lefkowitz@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
``National Study of the Hospital Adverse Event Reporting Follow-Up
Survey''
This proposed information collection will conduct a survey similar
to a previous AHRQ baseline survey conducted in 2005, which examined
and characterized adverse event reporting in the Nation's hospitals
(Farley DO, Haviland A, Champagne S, Jam AK, Battles JB, Munier WB,
Loeb JM. Adverse Event Reporting Practices by U.S. Hospitals: Results
of a National Survey, under review for publication). The follow-up
survey will allow AHRQ to examine how hospitals' use of adverse event
reporting systems has changed over time. The baseline survey was
completed by 1,652 hospital risk managers selected from a nationally
representative sample frame. The follow-up survey will consist of a
random sample of 1,200 of the respondents to the baseline survey. We
anticipate an 85% response rate for the follow-up survey, resulting in
1,020 completed questionnaires.
Similar to the baseline survey, the follow-up survey will ascertain
whether hospitals collect information on adverse events, and how the
information is stored. Information will also be collected regarding the
hospital's case definition of a reportable event, whether information
on the severity of the adverse event is collected, who might report
this information and whether they can report to a system which is
confidential and/or anonymous. The questionnaire also asks about the
uses of the data that are collected, and whether information is used
for purposes including analytic uses, personnel action, and improvement
interventions. Finally, the questionnaire asks about the other sources
of information that are useful to hospitals for patient safety-related
interventions.
This project is being conducted pursuant to AHRQ's statutory
mandates to (1) promote health care quality improvement by conducting
and supporting research that develops and presents scientific evidence
regarding all aspects of health care, including methods for measuring
quality and strategies for improving quality (42 U.S.C. 299(b)(1)(F))
and (2) conduct and support research on health care and on systems for
the delivery of such care, including activities with respect to quality
measurement and improvement (42 U.S.C. 299a(a)(2)). In addition,
Congress has, in report language, directed AHRQ to provide a report
detailing the results of its efforts to reduce medical errors. See
Report for the Departments of Labor, Health and Human Services, and
Education, and related agencies Appropriation Bill for Fiscal Year
2002, S. Rep. 107-84, at 11 (2001).
This project is being funded by AHRQ and conducted by the RAND
corporation as part of a contract under which RAND serves as the
Patient Safety Evaluation center for AHRQ's patient safety initiative.
Method of Collection
The baseline survey and data collection procedures have been
previously conducted and reviewed (under OMB Number 0935-0125,
Expiration Date 07/31/2008). The follow-up survey will include an
initial mailed survey with two waves of mailed follow-ups as needed,
and a computer-Assisted Telephone Interviewing (CATI) survey follow-up
for the remaining non-responders. The survey will be completed by one
Risk Manager per hospital.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden hours for the
respondents' time to participate in this information collection. The
questionnaire is expected to require 25 minutes to complete, resulting
in a total burden of 425 hours.
Exhibit 2 shows the estimated annualized cost burden for the
respondents, which is estimated to be $11,518. The respondents will not
incur any other costs beyond those associated with their time to
participate.
Exhibit 1.--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form name Number of responses per Hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Risk manager questionnaire...................... 1,020 1 25/60 425
---------------------------------------------------------------
Total....................................... 1,020 NA NA 425
----------------------------------------------------------------------------------------------------------------
[[Page 43239]]
Exhibit 2.--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Number of Total burden Average hourly Total cost
Form name respondents hours wage rate* burden
----------------------------------------------------------------------------------------------------------------
Risk manager questionnaire...................... 1,020 425 $27.10 $11,518
---------------------------------------------------------------
Total....................................... 1,020 425 NA 11,518
----------------------------------------------------------------------------------------------------------------
* Based upon the mean of the average wages, National Compensation Survey: Occupational wages in the United
States 2006, ``U.S. Department of Labor, Bureau of Labor Statistics.''
Estimated Annual Costs to the Federal Government
The Agency is supporting the conduct of this survey and analysis of
survey data as part of a contract with the RAND Corporation under which
RAND serves as the Patient Safety Evaluation Center for AHRQ's patient
safety initiative. The estimated cost for this work is $240,000,
including $190,000 for data collection activities and $50,000 to design
the study, analyze the data and report the findings.
Request for Comments
In accordance with the above-cited Paperwork Reduction Act
legislation, 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, quality improvement and 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: July 16, 2008.
Carolyn M. Clancy,
Director.
[FR Doc. E8-16874 Filed 7-23-08; 8:45 am]
BILLING CODE 4160-90-M