Agency Information Collection Activities: Proposed Collection; Comment Request, 80410-80412 [E8-30762]
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Clarian Health Partners, Inc ..................
Partners Limited .....................................
Atlantis Holdings LLC ............................
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Alltel Corporation.
Ball Memorial Hospital, Inc.
Norbord Inc.
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Windjammer Senior Equity Fund III, L.P.
Compass Group PLC .............................
SPC Partners II, L.P ..............................
Kimco Facilities Services Corporation ...
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Kimco Facilities Services Corporation.
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Prime Financial Credit Union .................
Guardian Credit Union ...........................
Guardian Credit Union.
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Platinum Equity Capital Partners II, L.P.
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326–3100.
By Direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. E8–30872 Filed 12–30–08; 8:45 am]
BILLING CODE 6750–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
pwalker on PROD1PC71 with NOTICES
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: ‘‘The
AHRQ Data Inventory.’’ In accordance
with the Paperwork Reduction Act of
VerDate Aug<31>2005
20:19 Dec 30, 2008
Jkt 217001
Stimson Lumber Company, Inc .............
Wavecom S.A ........................................
Tygris Commercial Finance Group, Inc
Tygris Commercial Finance Group, Inc
Stephen J. Williams ...............................
1995, 44 U.S.C. 3506(c)(2)(A), AHRQ
invites the public to comment on this
proposed information collection.
This proposed information collection
was previously published in the Federal
Register on October 24th, 2008 and
allowed 60 days for public comment.
One comment was received. The
purpose of this notice is to allow an
additional 30 days for public comment.
DATES: Comments on this notice must be
received by January 30, 2009.
ADDRESSES: Written comments should
be submitted to: AHRQ’s OMB Desk
Officer by fax at (202) 395–6974
(Attention: AHRQs desk officer) or by email at OIRA_submission@omb.eop.gov
(attention: AHRQ’s desk officer).
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: ‘‘The AHRQ Data
Inventory’’
The Agency for Healthcare Research
and Quality (AHRQ) is interested in
determining the availability of regularly
collected administrative and other data
collection initiatives about outpatient
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
Stimson Lumber Company, Inc.
Wavecom S.A.
Tygris Commercial Finance Group, Inc.
Tygris Commercial Finance Group, Inc.
International Offshore Services, LLC.
health service utilization. AHRQ seeks
to better understand issues in
developing data collection initiatives,
redundancies in these initiatives, uses
of available data, gaps in available
information, similarities across data
projects, and areas for possible
collaboration and coordination. AHRQ’s
initial focus is on those data sets that
would inform healthcare providers,
policymakers, and consumers about
outpatient health service utilization and
episodes of care.
The primary purpose of this
information collection is to
comprehensively document outpatient
health care data collection initiatives in
the 50 states, the District of Columbia,
and other geographic units. Information
being collected about the data sets is not
readily available to the public. In-depth
information about the data sets will
provide guidance to AHRQ on the
potential synergy across such initiatives
and suggest how the information can
inform Federal, State, and local health
care policymakers, clinicians, and
consumers. Information collected
during the interviews will
comprehensively document outpatient
health care data collection initiatives.
This project is important for several
reasons. First, many data collection
initiatives exist or are in the planning
E:\FR\FM\31DEN1.SGM
31DEN1
80411
Federal Register / Vol. 73, No. 251 / Wednesday, December 31, 2008 / Notices
stages, but there is limited collaboration
and synthesis among initiatives. With
limited resources and common goals, it
is imperative to understand the issues in
developing data collection initiatives,
redundancies in such initiatives, and
gaps in available information. Second,
with the increasing costs of health care,
it has become more important than ever
to use health services efficiently, yet
care and information about care is often
collected and delivered in isolation
without coordination across sites or
providers of care. The results of this
project will provide AHRQ and other
policymakers with the information they
need to serve as a catalyst to promote
coordinated standardization, reduce
redundancies, identify gaps in
information, and assist in further
development of needed data efforts.
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 the
costs and utilization of, and access to,
health care and the ways in which
health care services are organized,
delivered, and financed (42 U.S.C.
299(b)(l)(D) and (E)); (2) conduct and
support research on health care and on
systems for the delivery of such care (42
U.S.C. 299a(a)); and (3) conduct and
support research to advance the creation
of effective linkages between various
sources of health information (42 U.S.C.
299b–3(a)(3)).
Method of Collection
The survey will be initiated with an
e-mail message from AHRQ to
managers/administrators of each data
set selected for inclusion in the
Inventory. Data sets listed in the
inventory were identified from a search
of Web-based information about
outpatient and ambulatory patient care
data sets. The initial contact will be
followed by an e-mail distribution of a
cover letter and the questionnaire. The
cover letter will include information
about the purpose of the study, reason
respondents are being contacted,
information about the nondisclosure of
their responses, and a request to have
respondents review information
captured from the Internet about their
data sets. In addition, respondents will
be informed that they have the option to
complete and return the questionnaire
electronically or participate in a
telephone interview. Respondents who
do not return their questionnaires by the
requested time will get an e-mail
reminder. The e-mail reminder will be
followed by a telephone reminder.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annual
burden hours for the respondent’s time
to participate in this project. A
maximum of 80 respondents will
complete the survey questionnaire
which will require about 45 minutes to
complete. The total estimated burden
hours for this information collection is
60 hours.
Exhibit 2 show the estimated cost
burden based on the respondent’s time
to participate in this project. The total
cost burden is approximately $2,993.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Hours per
response
Total burden
hours
Inventory Survey ..............................................................................................
80
1
45/60
60
Total ..........................................................................................................
80
1
na
60
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents
Form name
Total burden
hours
Average
hourly wage
rate *
Total costs
burden
Inventory Survey ..............................................................................................
80
60
$49.89
$2,993
Total ..........................................................................................................
80
60
na
2,993
* Based upon the mean of general and operations managers (11–102 1), National Compensation Survey: Occupational Wages in the United
States 2007, U.S. Department of Labor, Bureau of Labor Statistics.
AHRQ health care research and health
care information dissemination
functions, including whether the
This one-year project is estimated to
information will have practical utility;
Cost component
Total cost
cost the government $136,000. Exhibit 3
(b) the accuracy of AHRQ’s estimate of
details the costs associated with this
Project Management ............
20,000.00 burden (including hours and costs) of
project, which include $11,000 for
Overhead ..............................
21,000.00 the proposed collection(s) of
project development, $72,500 for data
information; (c) ways to enhance the
collection and analysis, $12,000 for
Total ...............................
136,500.00
quality, utility, and clarity of the
preparing reports, $20,000 for project
information to be collected; and (d)
management and $21,000 for overhead.
Request for Comments
ways to minimize the burden of the
In accordance with the above-cited
collection of information upon the
EXHIBIT 3—PROJECT COSTS
Paperwork Reduction Act legislation,
respondents, including the use of
comments on AHRQ’s information
automated collection techniques or
Cost component
Total cost
collection are requested with regard to
other forms of information technology.
Comments submitted in response to
Project Development ............
$11,000.00 any of the following: (a) Whether the
this notice will be summarized and
Data Collection and Analysis
72,500.00 proposed collection of information is
Preparation of Reports .........
12,000.00 necessary for the proper performance of
included in the Agency’s subsequent
pwalker on PROD1PC71 with NOTICES
Estimated Annual Costs to the Federal
Government
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17:41 Dec 30, 2008
Jkt 217001
PO 00000
EXHIBIT 3—PROJECT COSTS—
Continued
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Federal Register / Vol. 73, No. 251 / Wednesday, December 31, 2008 / Notices
Prevention and the Agency for Toxic
Substances and Disease Registry.
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
BILLING CODE 4160–90–M
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Centers for Medicare & Medicaid
Services
Board of Scientific Counselors,
National Center for Injury Prevention
and Control: Notice of Charter
Amendment
pwalker on PROD1PC71 with NOTICES
Dated: December 17, 2008.
Carolyn M. Clancy,
Director.
[FR Doc. E8–30762 Filed 12–30–08; 8:45 am]
Dated: December 17, 2008.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E8–31111 Filed 12–30–08; 8:45 am]
Privacy Act of 1974; Notice of Modified
System of Records
This gives notice under the Federal
Advisory Committee Act (Pub. L. 92–
463) of October 6, 1972, that the
statutory requirements of the Advisory
Committee for Injury Prevention and
Control (ACIPC) have been transferred
to the Board of Scientific Counselors,
National Center for Injury Prevention
and Control (BSC, NCIPC).
The ACIPC was established on
October 18, 1988, in accordance with
Public Law 92–463, as amended (5
U.S.C. App. 2). Section 394(a) of the
Public Health Service Act, (42 U.S.C.
280b–2(a)), as amended, directed the
Secretary, Department of Health and
Human Services, acting through the
Director, CDC, to establish an advisory
committee to provide advice with
respect to the prevention and control of
injuries. On October 28, 1994, ACIPC
was reestablished under statute.
The responsibilities of ACIPC have
been assumed by the BSC, NCIPC. By
assuming the statutorily mandated
responsibilities of ACIPC, the BSC,
NCIPC will thereby become a statutorily
mandated committee, continuing to
serve the purposes set forth by Section
394(a) of the Public Health Service Act.
For information, contact Gwendolyn
Cattledge, Ph.D., Executive Secretary,
Board of Scientific Counselors, National
Center for Injury Prevention and
Control, Centers for Disease Control and
Prevention, Department of Health and
Human Services, 4770 Buford Highway,
Mailstop K02, Atlanta, Georgia 30341,
telephone (770) 488–4655 or fax (770)
488–4422.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
VerDate Aug<31>2005
17:41 Dec 30, 2008
Jkt 217001
AGENCY: Department of Health and
Human Services (HHS), Centers for
Medicare & Medicaid Services (CMS).
ACTION: Notice of a Modified System of
Records.
SUMMARY: In accordance with the
requirements of the Privacy Act of 1974,
CMS is proposing to make minor
amendments to an existing system of
records (SOR) titled, ‘‘Performance
Measurement and Reporting System
(PMRS),’’ System No. 09–70–0584,
published at 72 FR 52133 (September
12, 2007). PMRS serves as a master
system of records to assist in projects
that provide transparency in health care
on a broad scale enabling consumers to
compare the quality and price of health
care services so that they can make
informed choices among individual
physicians, practitioners, and other
providers of services. We are making
minor amendments to PMRS to include
two additional legal authorities: The
Medicare, Medicaid, and SCHIP
Extension Act of 2007 (MMSEA) (Pub.
L. 110–173) and the Medicare
Improvements for Patients and
Providers Act of 2008 (MIPPA) (Pub. L.
110–275). Section 101(b) of the MMSEA
amended section 1848(k)(2)(B) of the
Social Security Act (the Act) (42 U.S.C.
1395w–4) and section 101(c) of division
B of the Tax Relief and Health Care Act
of 2006 to extend the Physician Quality
Reporting Initiative (PQRI). MIPPA,
effective July 15, 2008, extended the
PQRI for 2010 and subsequent years and
authorized a new incentive program for
successful electronic prescribers under
section 1848(m)(2) of the Act. In
addition, the MIPPA requires the
Secretary to post on the CMS Web site
the names of eligible professionals or
group practices who satisfactorily
submit data on quality measures
through PQRI and the names of those
eligible professionals or group practices
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Frm 00052
Fmt 4703
Sfmt 4703
who are successful electronic
prescribers. This requirement is codified
at section 1848(m)(5)(G) of the Act.
Accordingly, CMS is adding §§ 131 and
132 of MIPPA, § 101 of MMSEA,
§ 1848(k) of the Act, and § 1848(m) of
the Act to the PMRS’ legal authority
section.
In addition, we are clarifying in this
notice that the term, ‘‘performance
measurement results’’ used in the PMRS
includes, but is not limited to,
submission of data on measures, eprescribing usage, frequency of
reporting or performance, as well as
rates or scores based on application of
specific measures. We consider all of
these types of information to be valid
indicators of a physician’s,
practitioner’s, or other provider’s
commitment to and delivery of high
quality, high value health care.
The primary purpose of this system is
to support the collection, maintenance,
and processing of information to
promote the delivery of high quality,
efficient, effective, and economical
health care services, and promoting the
quality and efficiency of services of the
type for which payment may be made
under title XVIII by allowing for the
establishment and implementation of
performance measures, the provision of
feedback to physicians, and public
reporting of performance information.
Information in this system will also be
disclosed to: (1) Support regulatory,
reimbursement, and policy functions
performed for the Agency or by a
contractor, consultant, or a CMS
grantee; (2) assist another Federal and/
or state agency, agency of a state
government, or an agency established by
state law; (3) promote more informed
choices by Medicare beneficiaries
among their Medicare group options by
making physician performance
measurement information available to
Medicare beneficiaries through a Web
site and other forms of data
dissemination; (4) provide CVEs and
data aggregators with information that
will assist in generating single or multipayer performance measurement results
to promote transparency in health care
to members of their community; (5)
assist individual physicians,
practitioners, providers of services,
suppliers, laboratories, and other health
care professionals who are participating
in health care transparency projects; (6)
assist individuals or organizations with
projects that provide transparency in
health care on a broad scale enabling
consumers to compare the quality and
price of health care services; or for
research, evaluation, and
epidemiological projects related to the
prevention of disease or disability;
E:\FR\FM\31DEN1.SGM
31DEN1
Agencies
[Federal Register Volume 73, Number 251 (Wednesday, December 31, 2008)]
[Notices]
[Pages 80410-80412]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-30762]
=======================================================================
-----------------------------------------------------------------------
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: ``The AHRQ Data Inventory.'' 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.
This proposed information collection was previously published in
the Federal Register on October 24th, 2008 and allowed 60 days for
public comment. One comment was received. The purpose of this notice is
to allow an additional 30 days for public comment.
DATES: Comments on this notice must be received by January 30, 2009.
ADDRESSES: Written comments should be submitted to: AHRQ's OMB Desk
Officer by fax at (202) 395-6974 (Attention: AHRQs desk officer) or by
e-mail at OIRA_submission@omb.eop.gov (attention: AHRQ's desk
officer).
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: ``The AHRQ Data Inventory''
The Agency for Healthcare Research and Quality (AHRQ) is interested
in determining the availability of regularly collected administrative
and other data collection initiatives about outpatient health service
utilization. AHRQ seeks to better understand issues in developing data
collection initiatives, redundancies in these initiatives, uses of
available data, gaps in available information, similarities across data
projects, and areas for possible collaboration and coordination. AHRQ's
initial focus is on those data sets that would inform healthcare
providers, policymakers, and consumers about outpatient health service
utilization and episodes of care.
The primary purpose of this information collection is to
comprehensively document outpatient health care data collection
initiatives in the 50 states, the District of Columbia, and other
geographic units. Information being collected about the data sets is
not readily available to the public. In-depth information about the
data sets will provide guidance to AHRQ on the potential synergy across
such initiatives and suggest how the information can inform Federal,
State, and local health care policymakers, clinicians, and consumers.
Information collected during the interviews will comprehensively
document outpatient health care data collection initiatives.
This project is important for several reasons. First, many data
collection initiatives exist or are in the planning
[[Page 80411]]
stages, but there is limited collaboration and synthesis among
initiatives. With limited resources and common goals, it is imperative
to understand the issues in developing data collection initiatives,
redundancies in such initiatives, and gaps in available information.
Second, with the increasing costs of health care, it has become more
important than ever to use health services efficiently, yet care and
information about care is often collected and delivered in isolation
without coordination across sites or providers of care. The results of
this project will provide AHRQ and other policymakers with the
information they need to serve as a catalyst to promote coordinated
standardization, reduce redundancies, identify gaps in information, and
assist in further development of needed data efforts.
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 the costs and
utilization of, and access to, health care and the ways in which health
care services are organized, delivered, and financed (42 U.S.C.
299(b)(l)(D) and (E)); (2) conduct and support research on health care
and on systems for the delivery of such care (42 U.S.C. 299a(a)); and
(3) conduct and support research to advance the creation of effective
linkages between various sources of health information (42 U.S.C. 299b-
3(a)(3)).
Method of Collection
The survey will be initiated with an e-mail message from AHRQ to
managers/administrators of each data set selected for inclusion in the
Inventory. Data sets listed in the inventory were identified from a
search of Web-based information about outpatient and ambulatory patient
care data sets. The initial contact will be followed by an e-mail
distribution of a cover letter and the questionnaire. The cover letter
will include information about the purpose of the study, reason
respondents are being contacted, information about the nondisclosure of
their responses, and a request to have respondents review information
captured from the Internet about their data sets. In addition,
respondents will be informed that they have the option to complete and
return the questionnaire electronically or participate in a telephone
interview. Respondents who do not return their questionnaires by the
requested time will get an e-mail reminder. The e-mail reminder will be
followed by a telephone reminder.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annual burden hours for the
respondent's time to participate in this project. A maximum of 80
respondents will complete the survey questionnaire which will require
about 45 minutes to complete. The total estimated burden hours for this
information collection is 60 hours.
Exhibit 2 show the estimated cost burden based on the respondent's
time to participate in this project. The total cost burden is
approximately $2,993.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form name Number of responses per Hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Inventory Survey................................ 80 1 45/60 60
---------------------------------------------------------------
Total....................................... 80 1 na 60
----------------------------------------------------------------------------------------------------------------
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Number of Total burden Average hourly Total costs
Form name respondents hours wage rate * burden
----------------------------------------------------------------------------------------------------------------
Inventory Survey................................ 80 60 $49.89 $2,993
---------------------------------------------------------------
Total....................................... 80 60 na 2,993
----------------------------------------------------------------------------------------------------------------
* Based upon the mean of general and operations managers (11-102 1), National Compensation Survey: Occupational
Wages in the United States 2007, U.S. Department of Labor, Bureau of Labor Statistics.
Estimated Annual Costs to the Federal Government
This one-year project is estimated to cost the government $136,000.
Exhibit 3 details the costs associated with this project, which include
$11,000 for project development, $72,500 for data collection and
analysis, $12,000 for preparing reports, $20,000 for project management
and $21,000 for overhead.
Exhibit 3--Project Costs
------------------------------------------------------------------------
Cost component Total cost
------------------------------------------------------------------------
Project Development..................................... $11,000.00
Data Collection and Analysis............................ 72,500.00
Preparation of Reports.................................. 12,000.00
Project Management...................................... 20,000.00
Overhead................................................ 21,000.00
---------------
Total............................................... 136,500.00
------------------------------------------------------------------------
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 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
[[Page 80412]]
request for OMB approval of the proposed information collection. All
comments will become a matter of public record.
Dated: December 17, 2008.
Carolyn M. Clancy,
Director.
[FR Doc. E8-30762 Filed 12-30-08; 8:45 am]
BILLING CODE 4160-90-M