99-27467. Proposed Data Collections Submitted for Public Comment and Recommendations  

  • [Federal Register Volume 64, Number 203 (Thursday, October 21, 1999)]
    [Notices]
    [Pages 56794-56795]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-27467]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Centers for Disease Control And Prevention
    [60Day-00-03]
    
    
    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, the Center for Disease Control and 
    Prevention is providing opportunity for public comment on proposed data 
    collection 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) 639-7090.
        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 for other 
    forms of information technology. Send comments to Seleda Perryman, CDC 
    Assistant Reports Clearance Officer, 1600 Clifton Road, MS-D24, 
    Atlanta, GA 30333. Written comments should be received within 60 days 
    of this notice.
    
    Proposed Projects
    
        1. Surveillance and Evaluation of Plasma Donors for the Human 
    Immunodeficiency Virus (HIV) and Hepatitis C Virus (HCV)--New--National 
    Center for HIV, STD, and TB Prevention (NCHSTP). In 1987, the President 
    directed the Department of Health and Human Services (DHHS) to 
    determine the nationwide incidence of, to predict the future of, and to 
    determine the extent to which human immunodeficiency virus (HIV) was 
    present in various segments of the population. In response, the CDC 
    formed an epidemiologic team to summarize existing information. An 
    extensive review of published and unpublished data led to the 
    conclusion that even though there was information suggesting a very 
    large number of Americans were infected, there was no substitute for 
    carefully and scientifically obtained incidence and prevalence data. 
    The need to monitor HIV seroprevalence existed on the national and at 
    the state and local levels for public health management: Targeting and 
    evaluating prevention programs, planning future health care needs and 
    determining health policy. Research has also indicated that similar 
    studies are needed to determine the incidence and prevalence of 
    hepatitis C (HCV) infection.
        A complementary family of surveys and studies, organized by the 
    CDC, provides empirical estimates of the extent of the epidemic of the 
    human immunodeficiency virus (HIV) in the United States. The national 
    surveillance system of HIV infection in the United States includes 
    monitoring incidence and prevalence rates of HIV-infection among first 
    time and repeat whole blood donors. Although this surveillance system 
    has been in place for several years to monitor HIV trends in the United 
    States blood supply, such a system does not exist for the source
    
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    plasma industry for either HIV or hepatitis C (HCV).
        The source plasma industry collects approximately 14 million of 
    plasma each year. The majority of source plasma is used to produce 
    immune globulins, albumin and other blood products utilized in the 
    United States and in other countries. Donors may donate up to two times 
    per week and are remunerated for each donation. Although the source 
    collection industry plays an important role in the production of blood 
    products, little information regarding HIV or HCV rates within the 
    industry has been published to date.
        The objectives of this study of HIV and HCV in plasma donors are 
    to:
        1. Analyze the risk behavior characteristics of infected donors to 
    assess distribution and trends of HIV and HCV;
        2. Study the motivations and risk factors of HIV and HCV infected 
    deferred donors in order to improve the donor screening and deferral 
    processes;
        3. Monitor additional human immunodeficiency and hepatitis viruses, 
    HIV and HCV genetic variation, and other infections relevant to the 
    epidemiology of HIV and HCV among U.S. plasma donors;
        4. Evaluate the laboratory characteristics of plasma from infected 
    donors to determine the effectiveness of current and anticipated test 
    modalities; and
        5. Evaluate risk factors for transmission of HCV among recently 
    infected individuals.
        The above objectives will be attained though a questionnaire 
    designed to evaluate demographic information, knowledge of HIV and HCV, 
    risks for HIV and HCV and motivations for donating plasma. In order to 
    elucidate risks for transmission among this population, a group of HIV 
    and HCV negative persons will also be given the questionnaire. 
    Respondents will be interviewed with the aid of a computer assisted 
    telephone interview (CATI) and respondents will receive a stipend for 
    their time and travel expenses. Participation is voluntary, and all 
    information will be gathered only after written informed consent has 
    been obtained.
        The CDC anticipates 430 individuals will be enrolled annually in 
    this study (based upon combined estimates obtained from the plasma 
    companies regarding the number of HIV and HCV positive donors 
    identified per year, plus the number of HIV and HCV negative 
    individuals enrolled as comparisons). It has been estimated that the 
    interview will take approximately 20 minutes to complete; therefore, 
    the response burden will be 143 hours. The approximate hourly wage 
    earned per respondent is $10.00/hour. The total cost to the respondents 
    would be $1430.00.
    
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                                                                      Number of     Avg. burden per
                      Form name                      Number of        responses/     response  (in     Total Burden
                                                    respondents       respondent         hrs.)          (in hrs.)
    ----------------------------------------------------------------------------------------------------------------
    Questionnaire...............................             430                1            20/60              143
    ----------------------------------------------------------------------------------------------------------------
    
        Date: October 14, 1999.
    Nancy Cheal,
    Acting Associate Director for Policy, Planning, and Evaluation, Centers 
    for Disease Control and Prevention (CDC).
    [FR Doc. 99-27467 Filed 10-20-99; 8:45 am]
    BILLING CODE 4163-18-P
    
    
    

Document Information

Published:
10/21/1999
Department:
Centers for Disease Control and Prevention
Entry Type:
Notice
Document Number:
99-27467
Dates:
October 14, 1999. Nancy Cheal, Acting Associate Director for Policy, Planning, and Evaluation, Centers for Disease Control and Prevention (CDC). [FR Doc. 99-27467 Filed 10-20-99; 8:45 am] BILLING CODE 4163-18-P
Pages:
56794-56795 (2 pages)
Docket Numbers:
60Day-00-03
PDF File:
99-27467.pdf