[Federal Register: November 20, 2008 (Volume 73, Number 225)]
[Notices]
[Page 70354-70355]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr20no08-67]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-08-0010]
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
The National Birth Defects Prevention Study (NBDPS)--Revision--
National Center on Birth Defects and Developmental Disabilities
(NCBDDD), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Address the following criteria provided in 5 CFR 1320.5(a): CDC has
been monitoring the occurrence of serious birth defects and genetic
diseases in Atlanta since 1967 through the Metropolitan Atlanta
Congenital Defects Program (MACDP). The MACDP is a population-based
surveillance system for birth defects in the 5 counties of Metropolitan
Atlanta, which is being requested for OMB clearance for three
additional years. Its primary purpose is to describe the spatial and
temporal patterns of birth defects occurrence and serves as an early
warning system for new Teratogens. In 1997, the Birth Defects Risk
Factor Surveillance (BDRFS) study, a case-control study of risk factors
for selected birth defects, became the National Birth Defects
Prevention Study (NBDPS). The major components of the study did not
change.
The NBDPS is a case-control study of major birth defects that
includes cases identified from existing birth defect surveillance
registries in nine states,
[[Page 70355]]
including metropolitan Atlanta. Control infants are randomly selected
from birth certificates or birth hospital records. Mothers of case and
control infants are interviewed using a computer-assisted telephone
interview. The interview is estimated to take one hour. A maximum of
thirty-six hundred interviews are planned, 2,700 cases and 900
controls, resulting in a maximum interview burden of 3,600 hours for
all Centers.
Parents are also asked to collect cheek cells from themselves and
their infants for DNA testing. The collection of cheek cells by the
mother, father, and infant is estimated to take about 10 minutes per
person. Each person will be asked to rub 1 brush inside the left cheek
and 1 brush inside the right cheek for a total of 2 brushes per person.
Collection of the cheek cells takes approximately 1-2 minutes, but the
estimate of burden is 10 minutes to account for reading and
understanding the consent form and specimen collection instructions and
mailing back the completed kits. The anticipated maximum burden for
collection of the cheek cells is 1,800 hours.
Information gathered from both the interviews and the DNA specimens
will be used to study independent genetic and environmental factors as
well as gene-environment interactions for a broad range of carefully
classified birth defects.
There are no costs to the respondents other than their time. The
total estimated annualized burden is 5,400 hours.
Estimated Annualized Burden Table
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Number of Avg. burden
Respondents Number of responses per per response
respondents respondent (In hours)
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NBDPS case/control interview.................................... 3,600 1 1
Biologic Specimen Collection.................................... 10,800 1 10/60
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Dated: November 13, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E8-27618 Filed 11-19-08; 8:45 am]
BILLING CODE 4163-18-P