[Federal Register: December 19, 2003 (Volume 68, Number 244)]
[Notices]
[Page 70798]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr19de03-64]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-14-04]
Proposed Data Collections Submitted for Public Comment and
Recommendations
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) 498-1210. Send written
comments to CDC, Desk Officer, Human Resources and Housing Branch, New
Executive Office Building, Room 10235, Washington, DC 20503 or by fax
to (202) 395-6974. Written comments should be received within 30 days
of this notice.
Proposed Project: Workplace Exacerbation of Asthma (OMB No. 0920-
0495)--Extension--National Institute for Occupational Safety and Health
(NIOSH), Centers for Disease Control and Prevention (CDC).
Work-related asthma is the most common lung disease seen in
occupational health clinics in the United States based on data from the
Association of Occupational and Environmental Clinics for 1991-1996.
Work-related asthma includes both new onset asthma initiated by
workplace exposures and pre-existing asthma exacerbated by workplace
environments, in both types of cases repeated exposure to asthmatic
agents can lead to chronic pulmonary impairment. The 1985 American
Thoracic Society statement ``What Constitutes an Adverse Health Effect
of Air Pollution'' identified exacerbation of asthma as one of the
serious effects of environmental air pollution. While anecdotal
evidence suggests that as many as one-half of work-related asthma
patients treated in occupational medicine clinics had pre-existing
asthma that was exacerbated by workplace conditions, there are few data
from studies in the United States to support this claim.
Three years ago, NIOSH requested approval from OMB to conduct a
three phase study. In Phase 1 (Baseline Study), a telephone interview
was conducted to address three specific aims: (1) To determine the
frequency of workplace exacerbation of asthma (WEA); (2) to determine
the circumstances at work associated with exacerbation of asthma; and
(3) to determine the social and economic costs associated with
workplace exacerbation of asthma. To date, the Baseline Study telephone
interviews have been completed for a total of 615 participants. Also,
patient care records have been obtained in order to ascertain cost of
care for asthma for each participant (Specific Aim 3).
Phase 2 (Validation Phase) is being conducted with a subset of
respondents from the Baseline Study. Employed respondents with and
without workplace exacerbation are being asked to conduct serial
spirometry with a portable device. These findings will serve as the
``gold standard'' to determine the sensitivity and specificity of a
self-report of workplace exacerbation of asthma (Specific Aim
4). As part of the serial testing, respondents complete a
diary and final brief telephone interview at the end of the serial
testing. Data collection for Phase 2 continues. The Paperwork Reduction
Act does not apply to Phase 2 of the study.
In Phase 3 (Follow-up Study), all respondents from the Baseline
Study will be asked to complete a follow-up telephone interview
approximately two years later to investigate whether workplace
exacerbation at baseline predicts an increase in asthma severity
(Specific Aim 5). We anticipate that interviewing for Phase 3
will continue through August, 2004.
The data collected in this study will be used to further understand
the frequency of workplace-exacerbated asthma, the social and economic
impacts of this problem, and the implication of self-reporting WEA for
subsequent asthma severity. This information can be used to prioritize
resources for addressing this problem. The data collected in this study
will also identify which jobs and exposures are likely to exacerbate
existing asthma, thus providing guidance on where to focus preventive
efforts. Collected data on the validity of self-reporting WEA will be
useful to both clinicians and researchers who attempt to treat or study
individuals with this problem. The annualized burden for this data
collection is 214 hours.
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Number of Average Burden
Respondents Number of responses per per Response
respondents respondent (in hours)
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Validation Study \*\............................................ (200) (1) (7.5)
Follow-up Study: Attempt to conduct an interview................ 465 1 5/60
Follow-up Study: Completed interviews........................... 349 1 30/60
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\*\ The Paperwork Reduction Act does not apply to the Validation Study.
Dated: December 11, 2003.
Alvin Hall,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. 03-31306 Filed 12-18-03; 8:45 am]
BILLING CODE 4163-18-P