Browse: Departments Dates Agencies
DOCUMENT ID: [30Day-14-04]
SUBJECT CATEGORY: Proposed Data Collections Submitted for Public Comment and Recommendations
DOCUMENT SUMMARY:
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) 4981210. 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) 3956974. Written comments should be received within 30 days of this notice.
Proposed Project: Workplace Exacerbation of Asthma (OMB No. 0920 0495)ExtensionNational Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention (CDC).
Workrelated 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 19911996. Workrelated asthma includes both new onset asthma initiated by workplace exposures and preexisting 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 onehalf of workrelated asthma patients treated in occupational medicine clinics had preexisting 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
selfreport of workplace exacerbation of asthma (Specific Aim
In Phase 3 (Followup Study), all respondents from the Baseline
Study will be asked to complete a followup telephone interview
approximately two years later to investigate whether workplace
exacerbation at baseline predicts an increase in asthma severity
(Specific Aim
The data collected in this study will be used to further understand
the frequency of workplaceexacerbated asthma, the social and economic
impacts of this problem, and the implication of selfreporting 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 selfreporting 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.
Number of Average Burden
Respondents Number of responses per per Response
respondents respondent (in hours)
Validation Study \*\............................................ (200) (1) (7.5)
Followup Study: Attempt to conduct an interview................ 465 1 5/60
Followup Study: Completed interviews........................... 349 1 30/60
\*\ 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. 0331306 Filed 121803; 8:45 am]
BILLING CODE 416318P
SUMMARY: Agency information collection activities; proposals, submissions, and approvals,
DOCUMENT BODY 2:
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) 4981210. 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) 3956974. Written comments should be received within 30 days of this notice.
Proposed Project: Workplace Exacerbation of Asthma (OMB No. 0920 0495)ExtensionNational Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention (CDC).
Workrelated 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 19911996. Workrelated asthma includes both new onset asthma initiated by workplace exposures and preexisting 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 onehalf of workrelated asthma patients treated in occupational medicine clinics had preexisting 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
selfreport of workplace exacerbation of asthma (Specific Aim
In Phase 3 (Followup Study), all respondents from the Baseline
Study will be asked to complete a followup telephone interview
approximately two years later to investigate whether workplace
exacerbation at baseline predicts an increase in asthma severity
(Specific Aim
The data collected in this study will be used to further understand
the frequency of workplaceexacerbated asthma, the social and economic
impacts of this problem, and the implication of selfreporting 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 selfreporting 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.
Number of Average Burden
Respondents Number of responses per per Response
respondents respondent (in hours)
Validation Study \*\............................................ (200) (1) (7.5)
Followup Study: Attempt to conduct an interview................ 465 1 5/60
Followup Study: Completed interviews........................... 349 1 30/60
\*\ 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. 0331306 Filed 121803; 8:45 am]
BILLING CODE 416318P
14 CFR Part 39 40 CFR Part 52 14 CFR Part 71 33 CFR Part 165 50 CFR Part 679 47 CFR Part 73 26 CFR Part 1 40 CFR Part 180 33 CFR Part 117 50 CFR Part 17 44 CFR Part 67 50 CFR Part 648 14 CFR Part 97 33 CFR Part 100 40 CFR Part 63 50 CFR Part 622 44 CFR Part 65 50 CFR Part 660 26 CFR Part 301 39 CFR Part 111 40 CFR Part 300 6 CFR Part 5 40 CFR Part 271 47 CFR Part 64 40 CFR Parts 52 and 81 50 CFR Part 665 44 CFR Part 64 10 CFR Part 50 49 CFR Part 571 47 CFR Part 76