# Agency Forms Undergoing Paperwork Reduction Act Review

> Briefs, arguments, decisions, and more.

URL: https://www.frixlaw.com/law-library/documents/fr%3A97-1475

## Record

- **Collection:** Federal Register
- **Document type:** Notice
- **Published:** January 22, 1997
- **Citation:** 62 FR 3292

## Text

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention
[30 DAY-26]

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 Office on (404) 639-7090. Send written
comments to CDC, Desk Officer; Human Resources and Housing Branch, New
Executive Office Building, Room 10235; Washington, DC 20503. Written
comments should be received within 30 days of this notice.
The following requests have been submitted for review since the
last publication date on January 16, 1997.

Proposed Project

Studies of Immunotoxicity in Occupational Groups--(0920-0333)--
Reinstatement--A number of chemicals to which U.S. workers are
potentially exposed, including metals such as lead and beryllium and
solvents such as carbon tetrachloride, have been found to be
immunotoxic in experimental animals. There is little data on
immunosuppression, hypersensitivity or autoimmune disease in workers
exposed to chemicals that are immunotoxic in experimental animals.
NIOSH has undertaken a coordinated series of studies to focus on
immune-system effects related to specific chemical exposures in the
workplace. In the previous three years, NIOSH conducted studies of lead
and egg protein exposed workers.
In this reinstatement of the program, it is anticipated that up to
six additional research studies will be conducted under this program.
Examples of chemicals for which studies are being considered are latex,
silica, and solvents. In most of these studies, the immune function of
a group of workers exposed to the chemical of interest, and not exposed
to any other known or potential immunotoxins, will be compared to the
immune function in a group of individuals with no occupational exposure
to known or suspected immunotoxins. In some studies, the immune
function in a group of individuals will be compared before and after
they have exposure to the potential immunotoxin. The primary
information collected will be data on the level of exposure to the
potential immunotoxin (as measured in the air in the breathing zone of
the respondent, and/or in the respondent's blood or urine) and data on
specific markers of the status of the immune system from blood or
saliva samples provided by the subjects. The questionnaire data will be
directed at demographic, lifestyle, and medical factors (other than the
exposure or condition of interest) which may influence the function of
the immune system. In selected studies, the questionnaire will be used
to assess the presence of respiratory symptoms, dermatologic conditions
and/or reproductive effects, if the literature indicates a potential
relationship to these health problems. Study populations will be
identified through telephone contact and follow-up site visits (if
needed) with workplace facilities that use the chemical of interest.
The total annual burden is 1607.

----------------------------------------------------------------------------------------------------------------
Avg.
No. of burden/
Respondent (form) No. of responses/ response Total burden
respondents respondent (in (in hrs.)
hrs.)
----------------------------------------------------------------------------------------------------------------
Interview and blood collection.............................. 600 1 1 600
Additional interview module (respiratory, dermatologic, or
reproductive).............................................. 600 1 .5 300
Peak flow measurement (hypersensitivity studies only)....... 200 28 .08 467
Allergy skin tests (hypersensitivity studies only).......... 200 1 1 200
Company interview........................................... 40 1 1 40
----------------------------------------------------------------------------------------------------------------

Dated: January 15, 1997.
William G. Johnson,
Acting Associate Director for Policy Planning and Evaluation, Centers
for Disease Control and Prevention (CDC).
[FR Doc. 97-1475 Filed 1-21-97; 8:45 am]
BILLING CODE 4163-18-P

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Source: Frix Law Library, https://www.frixlaw.com/law-library/documents/fr%3A97-1475. Public record. Not legal advice.
