Proposed Data Collections Submitted for Public Comment and Recommendations, 22557-22558 [E9-11128]
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22557
Federal Register / Vol. 74, No. 91 / Wednesday, May 13, 2009 / Notices
ANNUAL BURDEN ESTIMATES
Responses
per
respondent
Total
responses
Hours per
response
Total burden
hours
Form
Number of respondents
Survey of Consumers .......................
Survey of the Distributors of the
Consumer Tools.
Consumer Focus Groups ..................
563 ...................................................
40 .....................................................
1
1
563
40
0.5
0.5
281.5
20
4 sites × 16 focus group participants
per site = 64.
1
64
1.5
96
Total ...........................................
667 ...................................................
3
667
2.5
397.5
E-mail comments to
paperwork@hrsa.gov or mail the HRSA
Reports Clearance Officer, Room 10–33,
Parklawn Building, 5600 Fishers Lane,
Rockville, MD 20857. Written comments
should be received within 60 days of
this notice.
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.
Dated: May 5, 2009.
Alexandra Huttinger,
Director, Division of Policy Review and
Coordination.
[FR Doc. E9–11086 Filed 5–12–09; 8:45 am]
Proposed Project
The National Violent Death Reporting
System (NVDRS) OMB# 0920–0607—
Revision—National Center for Injury
Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–09–0607]
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
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 404–639–5960 or send
comments to Maryam I. Daneshvar, CDC
Acting Reports Clearance Officer, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an e-mail 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
VerDate Nov<24>2008
20:03 May 12, 2009
Jkt 217001
Background and Brief Description
Violence is an important public
health problem. In the United States,
homicide and suicide are the second
and third leading causes of death,
respectively, in the 1–34 year old age
group. Unfortunately, public health
agencies do not know much more about
the problem than the numbers and the
sex, race, and age of the victims, all
information obtainable from the
standard death certificate. Death
certificates, however, carry no
information about key facts necessary
for prevention such as the relationship
of the victim and suspect and the
circumstances of the deaths, thereby
making it impossible to discern
anything but the gross contours of the
problem. Furthermore, death certificates
are typically available 20 months after
the completion of a single calendar year.
Official publications of national violent
death rates, e.g. those in Morbidity and
Mortality Weekly Report, rarely use data
that is less than two years old. Public
health interventions aimed at a moving
target last seen two years ago may well
miss the mark.
Local and Federal criminal justice
agencies such as the Federal Bureau of
Investigation (FBI) provide slightly more
information about homicides, but they
do not routinely collect standardized
data about suicides, which are in fact
much more common than homicides.
The FBI´s Supplemental Homicide
Report (SHRs) does collect basic
information about the victim-suspect
PO 00000
Frm 00049
Fmt 4703
Sfmt 4703
relationship and circumstances related
to the homicide. SHRs do not link
violent deaths that are part of one
incident such as homicide-suicides. It
also is a voluntary system in which
some 10–20 percent of police
departments nationwide do not
participate. The FBI´s National Incident
Based Reporting System (NIBRS)
provides slightly more information than
SHRs, but it covers less of the country
than SHRs. NIBRS also only provides
data regarding homicides. Also, the
Bureau of Justice Statistics Reports does
not use data that is less than two years
old.
CDC therefore proposes to continue a
state-based surveillance system for
violent deaths that will provide more
detailed and timely information. It taps
into the case records held by medical
examiners/coroners, police, and crime
labs. Data is collected centrally by each
state in the system, stripped of
identifiers, and then sent to the CDC.
Information is collected from these
records about the characteristics of the
victims and suspects, the circumstances
of the deaths, and the weapons
involved. States use standardized data
elements and software designed by CDC.
Ultimately, this information will guide
states in designing programs that reduce
multiple forms of violence.
Neither victim families nor suspects
are contacted to collect this information.
It all comes from existing records and is
collected by state health department
staff or their subcontractors. Health
departments incur an average of 2.5
hours per death in identifying the
deaths from death certificates,
contacting the police and medical
examiners to get copies of or to view the
relevant records, abstracting all the
records, various data processing tasks,
various administrative tasks, data
utilization, training, communications,
etc.
This revision is a request to allow 10
new state health departments to be
added to the currently funded 17, if
funding becomes available. This may
bring the total to 27 by the year 2012.
E:\FR\FM\13MYN1.SGM
13MYN1
22558
Federal Register / Vol. 74, No. 91 / Wednesday, May 13, 2009 / Notices
Violent deaths include all homicides,
suicides, legal interventions, deaths
from undetermined causes, and
unintentional firearm deaths. The
average state will experience
approximately 1,000 such deaths each
year.
There is no cost to respondents to
participate other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Respondents
Number of
respondents
Number of
responses/
respondent
Average
burden/
response
(in hours)
Total burden
(in hours)
State Health Departments ...............................................................................
27
1,000
2.5
67,500
Dated: May 6, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E9–11128 Filed 5–12–09; 8:45 am]
Proposed Project
BILLING CODE 4163–18–P
AHRQ proposes to conduct a pretest
of the Consumer Assessment of
Healthcare Providers and Systems
(CAHPSR) Hospital Survey health
literacy module. The CAHPS program is
a multi-year initiative of the Agency for
Healthcare Research and Quality. AHRQ
first launched the program in October
1995 in response to concerns about the
lack of good information about the
quality of health plans from the
enrollees’ perspective. Numerous public
and private organizations collected
information on enrollee and patient
satisfaction, but the surveys varied from
sponsor to sponsor and often changed
from year to year. The CAHPSR program
was designed to make it possible to
compare survey results across sponsors
and over time, and to generate tools and
resources that sponsors can use to
produce understandable and usable
comparative information for consumers.
Over time, the program has expanded
beyond its original focus on health
plans to address a range of health care
services to meet the various needs of
health care consumers, purchasers,
health plans, providers, and
policymakers. Based on a literature
review and an assessment of currently
available questionnaires, AHRQ
identified the need to develop a health
literacy module for the CAHPSR
Hospital Survey. The intent of the
planned module is to examine patients’
perspectives on how well health
information is communicated to them
by healthcare professionals in the
hospital setting. The objective of the
new module is to provide information to
health plans, hospitals, clinicians, group
practices, and other interested parties
regarding the quality of health
information delivered to patients. The
set of questions about health literacy
will be evaluated as a supplement to the
CAHPSR Hospital Survey.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Conunent 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: ‘‘Health
Literacy Item Set Supplemental to
CAHPS Hospital Survey—Pretest of
Proposed Questions and Methodology.’’
In accordance with the Paperwork
Reduction Act of 1995, Public Law 104–
13 (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 July 13, 2009.
Written comments should
be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by email at doris.lefkowit@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:
VerDate Nov<24>2008
18:44 May 12, 2009
Jkt 217001
‘‘Health Literacy Item Set Supplemental
to CAHPS Hospital Survey—Pretest of
Proposed Questions and Methodology’’
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
This study will be conducted for
AHRQ by its contactor, RAND
Corporation. It is being conducted
pursuant to AHRQ’s statutory authority
to conduct research and evaluations on
health care and systems for the delivery
of such care, including activities with
respect to the quality, effectiveness,
efficiency, appropriateness and value of
health care services. See 42 U.S.C.
299a(a)(1).
This study is a one-time field test to
be completed in the calendar years 2009
and 2010. The field test to be conducted
under this request will be done for the
following purposes:
a. Analysis of item wording—Assess
candidate wordings for items.
b. Analysis of participation rate—
Evaluate the overall response rate and
the proportion of that obtained from
mail versus telephone modes of data
collection.
c. Case mix adjustment analysis—
Evaluate variables that need to be
considered for case mix adjustment of
scores.
d. Psychometric Analysis—Provide
information for the revision of the
health literacy item set based on the
assessment of the reliability and
validity.
The end result will be collection of
the data related to the assessment of
patients’ perspective on how well health
information is communicated to them
by health care professionals in hospital
setting. The field testing will ensure that
future data collections yield high
quality data and minimize respondent
burden, increase agency efficiency, and
improve responsiveness to the public.
The survey items will be added to
currently available CAHPS R surveys
and will enhance the ability of hospitals
to assess the quality of their services.
Method of Collection
The potential respondent universe is
persons who had at least one overnight
stay at a hospital within the previous
five months. Excluded from the study
will be those who were less than 18
years old at the time of their admission,
had a psychiatric diagnosis, were
E:\FR\FM\13MYN1.SGM
13MYN1
Agencies
[Federal Register Volume 74, Number 91 (Wednesday, May 13, 2009)]
[Notices]
[Pages 22557-22558]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-11128]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-09-0607]
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 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 404-639-5960 or
send comments to Maryam I. Daneshvar, CDC Acting Reports Clearance
Officer, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail
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
The National Violent Death Reporting System (NVDRS) OMB
0920-0607--Revision--National Center for Injury Prevention and Control
(NCIPC), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Violence is an important public health problem. In the United
States, homicide and suicide are the second and third leading causes of
death, respectively, in the 1-34 year old age group. Unfortunately,
public health agencies do not know much more about the problem than the
numbers and the sex, race, and age of the victims, all information
obtainable from the standard death certificate. Death certificates,
however, carry no information about key facts necessary for prevention
such as the relationship of the victim and suspect and the
circumstances of the deaths, thereby making it impossible to discern
anything but the gross contours of the problem. Furthermore, death
certificates are typically available 20 months after the completion of
a single calendar year. Official publications of national violent death
rates, e.g. those in Morbidity and Mortality Weekly Report, rarely use
data that is less than two years old. Public health interventions aimed
at a moving target last seen two years ago may well miss the mark.
Local and Federal criminal justice agencies such as the Federal
Bureau of Investigation (FBI) provide slightly more information about
homicides, but they do not routinely collect standardized data about
suicides, which are in fact much more common than homicides. The
FBI[acute]s Supplemental Homicide Report (SHRs) does collect basic
information about the victim-suspect relationship and circumstances
related to the homicide. SHRs do not link violent deaths that are part
of one incident such as homicide-suicides. It also is a voluntary
system in which some 10-20 percent of police departments nationwide do
not participate. The FBI[acute]s National Incident Based Reporting
System (NIBRS) provides slightly more information than SHRs, but it
covers less of the country than SHRs. NIBRS also only provides data
regarding homicides. Also, the Bureau of Justice Statistics Reports
does not use data that is less than two years old.
CDC therefore proposes to continue a state-based surveillance
system for violent deaths that will provide more detailed and timely
information. It taps into the case records held by medical examiners/
coroners, police, and crime labs. Data is collected centrally by each
state in the system, stripped of identifiers, and then sent to the CDC.
Information is collected from these records about the characteristics
of the victims and suspects, the circumstances of the deaths, and the
weapons involved. States use standardized data elements and software
designed by CDC. Ultimately, this information will guide states in
designing programs that reduce multiple forms of violence.
Neither victim families nor suspects are contacted to collect this
information. It all comes from existing records and is collected by
state health department staff or their subcontractors. Health
departments incur an average of 2.5 hours per death in identifying the
deaths from death certificates, contacting the police and medical
examiners to get copies of or to view the relevant records, abstracting
all the records, various data processing tasks, various administrative
tasks, data utilization, training, communications, etc.
This revision is a request to allow 10 new state health departments
to be added to the currently funded 17, if funding becomes available.
This may bring the total to 27 by the year 2012.
[[Page 22558]]
Violent deaths include all homicides, suicides, legal interventions,
deaths from undetermined causes, and unintentional firearm deaths. The
average state will experience approximately 1,000 such deaths each
year.
There is no cost to respondents to participate other than their
time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden/
Respondents Number of responses/ response (in Total burden
respondents respondent hours) (in hours)
----------------------------------------------------------------------------------------------------------------
State Health Departments.................... 27 1,000 2.5 67,500
----------------------------------------------------------------------------------------------------------------
Dated: May 6, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E9-11128 Filed 5-12-09; 8:45 am]
BILLING CODE 4163-18-P