[Federal Register: May 21, 2004 (Volume 69, Number 99)]
[Notices]
[Page 29311-29312]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr21my04-91]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-04-54]
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 the CDC Reports
Clearance Officer on (404) 498-1210.
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. Send comments to Sandra Gambescia, CDC
Assistant Reports Clearance Officer, 1600 Clifton Road, MS-E11,
Atlanta, GA 30333 or send an e-mail to omb@cdc.gov. Written comments
should be received within 60 days of this notice.
Proposed Project
Gonococcal Isolate Surveillance Project (GISP) (OMB Control No.
0920-0307)--Extension--National Center for HIV, STD, and TB Prevention
(NCHSTP), Centers for Disease Control and Prevention (CDC).
CDC is requesting OMB approval for a 3-year extension of the
Gonococcal Isolate Surveillance Project (GISP), OMB Control No. 0920-
0307. The objectives of GISP are to: (1) Monitor trends in
antimicrobial susceptibility of strains of Neisseria gonorrhoeae in the
U.S. and (2) characterize resistant isolates. GISAP provides critical
surveillance for antimicrobial resistance, allowing for informed
treatment recommendations. GISP was begun in 1986 as a voluntary
surveillance project and has involved 5 regional laboratories and 28
publicly funded sexually transmitted disease (STD) clinics around the
country. The STD clinics submit up to 25 gonococcal isolates per month
to the regional laboratories, which measure susceptibility to a panel
of antibiotics. Limited demographic and clinical information
corresponding to the isolates are submitted directly by the clinics to
CDC.
During 1986-2003, GISP has demonstrated the ability to effectively
achieve its objectives. The emergence of resistance in the U.S. to
fluoroquinolones, commonly used therapies for gonorrhea was identified
through GISP and makes ongoing surveillance critical. Emergence of
decreased susceptibility to fluoroquinolones among the men having sex
with men (MSM) population in the U.S. was also identified through GISP
in 2003. Data gathered through GISP were used to change the treatment
for gonorrhea for the MSM population in April, 2004.
Under the GISP protocol, clinics are asked to provide 25 isolates
per month. However, due to low volume at some site, clinics submit an
average of 19 isolates per clinic per month, providing an average of
108 isolates per laboratory per month. For this data collection, a
``response'' is defined as the laboratory processing and data
collection/processing associated with an individual gonococcal isolate
from an individual patient. Based on previous laboratory experience in
analyzing the gonococcal isolates, the estimated burden for each
participating laboratory is 1 hour per response. This time estimate
includes the time to record control strain data. We estimate 108
gonococcal isolates per laboratory each month (total number of
responses per 5 laboratories is 1,296). The estimated time for clinical
personnel to abstract data is 11 minutes per response (19 isolates per
clinic per month). The estimated annualized burden for this data
collection is 7,650 hours. There is no cost to respondents.
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Average
Number of Number of burden per Total burden
Respondent respondents responses per response (in (in hours)
respondent hours)
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Laboratory...................................... 5 1,296 1 6,480
Clinic.......................................... 28 228 11/60 1,170
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Total....................................... 33 .............. .............. 7,650
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[[Page 29312]]
Dated: May 17, 2004.
Alvin Hall,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. 04-11528 Filed 5-20-04; 8:45 am]
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