Agency Forms Undergoing Paperwork Reduction Act Review, 4577-4578 [E8-1260]
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4577
Federal Register / Vol. 73, No. 17 / Friday, January 25, 2008 / Notices
Dated: January 16, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–1257 Filed 1–24–08; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–08–07BR]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an
e-mail to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
National Survey of Residential Care
Facilities (NSRCF) 2008–2010—New—
National Center for Health Statistics
(NCHS), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on the extent and nature of
illness and disability of the population
of the United States.
The National Survey of Residential
Care Facilities (NSRCF) is a new
collection. It is designed to complement
data collected by other federal surveys
and to fill a significant data gap about
a major portion of the long-term care
population. Data from the NSRCF will
provide a database on residential care
facilities that researchers and
policymakers can use to address a wide
array of research and policy questions.
The survey will utilize a computerassisted personal interviewing (CAPI)
system to collect information about
facility and resident characteristics.
This computerized system speeds the
flow of data making it possible to
release information on a more timely
basis and makes it easier for
respondents to participate in the survey.
A stratified random sample of
residential care facilities across four
strata (small, medium, large and extra
large) will be selected to participate in
the NSRCF. Within each facility a
random sample of residents will be
selected. To be eligible a facility must
have four or more beds, be licensed,
certified, or registered and provide or
arrange for 24 hour supervision and
personal care services for residents.
The facility questionnaire will collect
data about facility characteristics (size,
age, types of rooms), services offered,
characteristics of the resident
population, facility policies and
services, costs of services, and
background of the administrator. The
Resident Questionnaire collects
information on resident demographics,
current living arrangements within the
facility, involvement in activities, use of
services, charges for care, health status,
and cognitive and physical functioning.
In the pretest 25 facility
administrators, and 25 facility staff
serving as respondents will be
interviewed on an annualized basis, for
a total of 75 facilities. Residents
themselves will not be interviewed. For
the national survey, approximately
2,250 facilities will be surveyed for an
annual average of 750. Information on
an average of 5 residents each will be
collected.
Anticipated users of NSRCF data
include, but are not limited to the CDC;
the Congressional Research Office; the
Bureau of Health Professions, Health
Resources and Services Administration;
the Office of the Assistant Secretary for
Planning and Evaluation (ASPE); the
Agency for Healthcare Research and
Quality; the American Association of
Homes and Services for the Aging; the
National Hospice and Palliative Care
Organization; American Health Care
Association, Centers for Medicare and
Medicaid Services (CMS), Bureau of the
Census; and AARP. Other users of these
data include universities, contract
research organizations, many in the
private sector, foundations, and a
variety of users in the print media.
There is no cost to respondents other
than their time to participate. The total
estimated annualized burden hours are
2,778.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Number of
responses
per
respondent
Average
burden per
response
(in hours)
Pretest
Facility
Facility
Facility
Facility
Administrator (Facility Screener) .....................................................................................
Administrator (Advance Data Collection Form) ..............................................................
Administrator (Facility Questionnaire) .............................................................................
Staff (Resident Questionnaire) ........................................................................................
25
25
25
25
1
1
1
5
10/60
15/60
40/60
30/60
750
750
750
750
1
1
1
5
10/60
15/60
40/60
30/60
National Survey
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Facility
Facility
Facility
Facility
Administrator (Facility Screener) .....................................................................................
Administrator (Advance Data Collection Form) ..............................................................
Administrator (Facility Questionnaire) .............................................................................
Staff (Resident Questionnaire) ........................................................................................
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4578
Federal Register / Vol. 73, No. 17 / Friday, January 25, 2008 / Notices
Dated: January 16, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–1260 Filed 1–24–08; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4163–18–P
[Docket Number NIOSH–123]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Notice of Opportunity for Public to
Provide NIOSH with Comment:
Positive-Pressure Closed-Circuit SelfContained Breathing Apparatus
Centers for Disease Control and
Prevention
AGENCY:
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): FY 2008
National Office of Public Health
Genomics (NOPHG) Seed Grants
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the aforementioned meeting:
jlentini on PROD1PC65 with NOTICES
Time and Date:
1 p.m.–5 p.m., February 11, 2008 (Closed).
1 p.m.–5 p.m., February 12, 2008 (Closed).
1 p.m.–5 p.m., February 13, 2008 (Closed).
1 p.m.–5 p.m., February 14, 2008 (Closed).
1 p.m.–5 p.m., February 15, 2008 (Closed).
1 p.m.–5 p.m., February 19, 2008 (Closed).
Place: Teleconference.
Status: The meeting will be closed to the
public in accordance with provisions set
forth in section 552b(c) (4) and (6), Title 5
U.S.C., and the Determination of the Director,
Management Analysis and Services Office,
CDC, pursuant to Public Law 92–463.
Matters To Be Discussed: The meeting will
include the review, discussion, and
evaluation of proposals submitted in
response to the FY 2008 NOPHG Seed Grants
announcement.
Contact Person for More Information:
Brenda Colley Gilbert, Director, Extramural
Research Program Office, Coordinating
Center for Health Promotion, CDC, 1600
Clifton Road, NE., Mailstop K92, Atlanta, GA
30333, Telephone (770) 488–8390.
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 CDC and the Agency for Toxic
Substances and Disease Registry.
Dated: January 18, 2008.
Diane Allen,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. E8–1274 Filed 1–24–08; 8:45 am]
BILLING CODE 4163–18–P
VerDate Aug<31>2005
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Centers for Disease Control and
Prevention
The National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services.
ACTION: (1) Notice of opportunity for
public to provide NIOSH with comment
on the public’s reevaluation of NIOSH
limitations on and precaution for safe
use of positive-pressure closed-circuit
self-contained breathing apparatus,
Authority: Public Law 91–596.
(2) Notice of opportunity for
manufacturers and stakeholders to
provide NIOSH with input on the
NIOSH prohibition against using a
respirator which uses a breathing gas of
pure oxygen during direct exposure to
open flames and/or high radiant heat.
SUMMARY: The NIOSH, National
Personal Protective Technology
Laboratory (NPPTL), is currently
reevaluating its limitations on and
precaution for safe use of positivepressure closed-circuit self-contained
breathing apparatus. As stated in the
Federal Register (Vol. 50, No. 222,
pages 47456–47457 dated Monday,
November 18, 1985) NIOSH’s position
on this topic is that:
Available information does not
demonstrate to the satisfaction of NIOSH that
positive-pressure closed-circuit selfcontained breathing apparatus which use a
breathing gas of pure oxygen can be used
during direct exposure to open flames and/
or high radiant heat and assure the wearer’s
safety. Therefore, NIOSH has determined that
until it has been demonstrated to the
satisfaction of NIOSH that those devices can
be worn under such conditions, it is prudent
to presently limit the use of positive-pressure
closed-circuit self-contained breathing
apparatus which use pure oxygen breathing
gas to mines and mining atmospheres which
do not involve exposure to open flames or
high radiant heat.
Background: NIOSH/NPPTL is
currently developing performance
concepts as part of the rulemaking
process to develop a Closed-Circuit SelfContained Breathing Apparatus (CC–
SCBA) Module. This process has
identified that flame and heat durability
requirements need to be considered as
part of the module. On possible
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Frm 00063
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inclusion to the requirements is the
National Fire Protection Agency (NFPA)
Heat and Flame Test, NFPA 1981,
Section 8.11. NIOSH has conducted
laboratory testing on two (2) different
manufacturer’s apparatus. In the initial
testing, NFPA testing procedures were
followed with the exception that a
‘‘dummy’’ cylinder was used in lieu of
the oxygen cylinder. Test results were
encouraging and were presented at
NIOSH/NPPTL public meetings held on
July 19, 2005 and on October 12, 2006.
Arrangements are being made to
conduct the same tests with full oxygen
cylinders.
Additional research was garnered
through testing conducted at a second
laboratory. NPPTL personnel witnessed
a Flame Engulfment Test. In Germany,
Department 8 of the Association for the
Promotion of German Fire Safety
(VFDB) has included in its Guideline
0802 the same requirements for CloseCircuit Breathing Apparatus that has
been written into the draft European
Standard EN137 for Open-circuit
Compressed Air Breathing Apparatus
for flame engulfment. In this Directive,
if special thermal loads for protective
equipment cannot be excluded during
tactical operation, the device must pass
the flame engulfment test which is
described in Appendix D. Their flame
engulfment test is similar to NFPA’s. In
addition, this directive requires that
when using closed-circuit compressed
air breathing apparatus, type positive
pressure with mixed gas supply (N2, O2)
with an oxygen content of ≥ 30% by
volume in the breathing circuit risks by
oxygen emerging from a leakage in the
mask cannot be excluded. These devices
must pass the oxygen flame engulfment
test procedure described in appendix G
as follows:
• Simulate possible oxygen
enrichment under a firefighter helmet
according to EN 443 through a defined
leakage in the respiratory protective
mask (2.5 mm, 10 mm above the right
temple strap). The test set-up simulates
real conditions by equipping the test
head with real hair, a flame protection
hood and the respective neck curtains.
• Flame engulfment test is in
accordance with Appendix D
Æ Device is attached to a test dummy
and preheated in an oven at 90 ± 5° C
for 15 minutes
Æ Complete unit is then exposed to
direct flames for 10 seconds
Æ Test dummy with the apparatus is
then lifted to 150 ± 5/0 mm and
dropped
Æ During the entire test, the device is
connected to a breathing machine. The
pass/fail criteria are:
E:\FR\FM\25JAN1.SGM
25JAN1
Agencies
[Federal Register Volume 73, Number 17 (Friday, January 25, 2008)]
[Notices]
[Pages 4577-4578]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-1260]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-08-07BR]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-6974.
Written comments should be received within 30 days of this notice.
Proposed Project
National Survey of Residential Care Facilities (NSRCF) 2008-2010--
New--National Center for Health Statistics (NCHS), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health Service (PHS) Act (42 U.S.C.
242k), as amended, authorizes that the Secretary of Health and Human
Services (DHHS), acting through NCHS, shall collect statistics on the
extent and nature of illness and disability of the population of the
United States.
The National Survey of Residential Care Facilities (NSRCF) is a new
collection. It is designed to complement data collected by other
federal surveys and to fill a significant data gap about a major
portion of the long-term care population. Data from the NSRCF will
provide a database on residential care facilities that researchers and
policymakers can use to address a wide array of research and policy
questions. The survey will utilize a computer-assisted personal
interviewing (CAPI) system to collect information about facility and
resident characteristics. This computerized system speeds the flow of
data making it possible to release information on a more timely basis
and makes it easier for respondents to participate in the survey.
A stratified random sample of residential care facilities across
four strata (small, medium, large and extra large) will be selected to
participate in the NSRCF. Within each facility a random sample of
residents will be selected. To be eligible a facility must have four or
more beds, be licensed, certified, or registered and provide or arrange
for 24 hour supervision and personal care services for residents.
The facility questionnaire will collect data about facility
characteristics (size, age, types of rooms), services offered,
characteristics of the resident population, facility policies and
services, costs of services, and background of the administrator. The
Resident Questionnaire collects information on resident demographics,
current living arrangements within the facility, involvement in
activities, use of services, charges for care, health status, and
cognitive and physical functioning.
In the pretest 25 facility administrators, and 25 facility staff
serving as respondents will be interviewed on an annualized basis, for
a total of 75 facilities. Residents themselves will not be interviewed.
For the national survey, approximately 2,250 facilities will be
surveyed for an annual average of 750. Information on an average of 5
residents each will be collected.
Anticipated users of NSRCF data include, but are not limited to the
CDC; the Congressional Research Office; the Bureau of Health
Professions, Health Resources and Services Administration; the Office
of the Assistant Secretary for Planning and Evaluation (ASPE); the
Agency for Healthcare Research and Quality; the American Association of
Homes and Services for the Aging; the National Hospice and Palliative
Care Organization; American Health Care Association, Centers for
Medicare and Medicaid Services (CMS), Bureau of the Census; and AARP.
Other users of these data include universities, contract research
organizations, many in the private sector, foundations, and a variety
of users in the print media. There is no cost to respondents other than
their time to participate. The total estimated annualized burden hours
are 2,778.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Pretest
----------------------------------------------------------------------------------------------------------------
Facility Administrator (Facility Screener)...................... 25 1 10/60
Facility Administrator (Advance Data Collection Form)........... 25 1 15/60
Facility Administrator (Facility Questionnaire)................. 25 1 40/60
Facility Staff (Resident Questionnaire)......................... 25 5 30/60
----------------------------------------------------------------------------------------------------------------
National Survey
----------------------------------------------------------------------------------------------------------------
Facility Administrator (Facility Screener)...................... 750 1 10/60
Facility Administrator (Advance Data Collection Form)........... 750 1 15/60
Facility Administrator (Facility Questionnaire)................. 750 1 40/60
Facility Staff (Resident Questionnaire)......................... 750 5 30/60
----------------------------------------------------------------------------------------------------------------
[[Page 4578]]
Dated: January 16, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E8-1260 Filed 1-24-08; 8:45 am]
BILLING CODE 4163-18-P