98-2677. Proposed Data Collections Submitted for Public Comment and Recommendations  

  • [Federal Register Volume 63, Number 23 (Wednesday, February 4, 1998)]
    [Notices]
    [Pages 5806-5807]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-2677]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Centers for Disease Control and Prevention
    [INFO-98-11]
    
    
    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 for opportunity for public comment on 
    proposed data collection projects, the Centers for Disease Control and 
    Prevention (CDC) will publish periodic summaries of proposed 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 Wilma Johnson, CDC 
    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. A Longitudinal Study of Lead Poisoning from the Maternal Infant 
    Relationship Through Early Childhood--New--
        The Agency for Toxic Substances and Disease Registry (ATSDR) is 
    mandated pursuant to the 1980 Comprehensive Environmental Response 
    Compensation and Liability Act (CERCLA), and its 1986 Amendments, The 
    Superfund Amendments and Reauthorization Act (SARA), to prevent or 
    mitigate adverse human health effects and diminished quality of life 
    resulting from exposure to hazardous substances in the environment. 
    Lead exposure has been associated with negative pregnancy outcomes in 
    humans, including low birth weight, spontaneous abortion, congenital 
    malformation, and various neurological effects in newborns and young 
    children. The level of lead considered to be toxic has been lowered 
    over the years by major research groups, organizations, and agencies. 
    While lead has been shown to affect all organs, the brain or nervous 
    system seems to be the most sensitive to lead toxicity, especially in 
    young children. Blood lead levels as low as 10 g/dL have been 
    shown to result in delayed cognitive development, reduced IQ scores, 
    and impaired hearing.
        This study, originally approved by OMB in 1995, examines the long-
    term effects of low and marginal toxic blood lead levels in neonates 
    and preschool African-American children in the Atlanta area. This study 
    is divided into two components, (i) Prevalence of lead exposure in 
    children of preschool age and (ii) longitudinal health effects of low 
    and marginal lead exposure. These studies are conducted concurrently.
        The primary focus of the prevalence study is the evaluation of the 
    relationship between socio-economic status, elemental blood lead levels 
    within the home environment, and blood lead levels of preschool aged 
    children. The objective of the longitudinal study is the evaluation of 
    the relationship between lead levels found in maternal and cord blood 
    and adverse health effects in the infant, including deficits in 
    behavioral, cognitive and physical development. To correlate cognitive 
    and behavioral development with varying blood lead levels, each newborn 
    is to undergo a series of psychometric testing at birth, then again at 
    6 months, 1, and 2 years of age. Evaluations of physician development 
    will be conducted by reviewing the medical records of each newborn 
    within the first year after birth.
        This request is for a 3-year extension of the current OMB approval; 
    however we are requesting a new OMB authority (and number) as the old 
    number (0923-0015) will now apply only to the Substance Specific 
    Applied Research Program (AMHPS) [King/Drew Lead Study in-Person 
    Interview, Lead and Hypertension Screening Questionnaire/Risk Factor 
    Questionnaire]. The requests for OMB approval for the two studies has 
    been separated, with the King/Drew investigation retaining the old OMB 
    number (0923-0015).
    
    [[Page 5807]]
    
    
    
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                                                                               No. of     Avg. burden/              
                   Study                     Respondents          No. of     responses/   response (in  Total burden
                                                               respondents   respondent       hrs.)       (in hrs.) 
    ----------------------------------------------------------------------------------------------------------------
    Prevalence........................  Households...........          100           1           0.75          75   
                                        Daycare Centers......           10           1           0.25           2.5 
    Longitudinal......................  Pregnant Women.......          300           3.5         0.167        175.35
                                        Infants..............          300           7           0.524      1,100.40
                                       -----------------------------------------------------------------------------
        Total.........................  .....................  ...........  ............  ............      1,353.25
    ----------------------------------------------------------------------------------------------------------------
    
        2. Weekly and Annual Morbidity and Mortality Reports--In 1878 
    Congress authorized the U.S. Marine Hospital Service (later re-named 
    the U.S. Public Health Service) to collect morbidity reports on 
    cholera, smallpox, plague, and yellow fever from U.S. consuls overseas; 
    this information was to be used for instituting quarantine measures to 
    prevent the introduction and spread of these diseases in the United 
    States. In 1879, a specific Congressional appropriation was made for 
    the collection and publication of reports of these notifiable diseases. 
    The authority for weekly reporting and publication was expanded by 
    Congress in 1893 to include data from state and municipal authorities 
    throughout the U.S. To increase the uniformity of the data, Congress 
    enacted a law in 1902 directing the Surgeon General of the Public 
    Health Service to provide forms for the collection and compilation of 
    data and for the publication of reports at the national level.
        In 1961, responsibility for the collection of data on nationally 
    notifiable diseases and deaths in 121 U.S. cities was transferred from 
    the National Office of Vital Statistics to CDC. For 37 years the MMWR 
    has consistently served as CDC's main communication mode for disease 
    outbreaks and trends in health and health behavior. In collaboration 
    with the Council of State and Territorial Epidemiologists (CSTE), CDC 
    has demonstrated the efficiency and effectiveness of computer 
    transmission of data. The data collected electronically for publication 
    in the MMWR provides information which CDC and State epidemiologists 
    use to detail and more effectively interrupt outbreaks. Reporting also 
    provides the timely information needed to measure and demonstrate the 
    impact of changed immunization laws or a new therapeutic measure. Users 
    of data include, but are not limited to, congressional offices, state 
    and local health agencies, health care providers, and other health 
    related groups.
        The dissemination of public health information is accomplished 
    through the MMWR series of publications. The publications consist of 
    the MMWR, the CDC Surveillance Summaries, the Recommendations and 
    Reports, and the Annual Summary of Notifiable Diseases. The total cost 
    to respondents is estimated to be $48,100.
    
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                                                                          No. of       Avg. burden/                 
                       Respondents                         No.of        responses/     response (in    Total burden 
                                                        respondents     respondent         hrs.)         (in hrs.)  
    ----------------------------------------------------------------------------------------------------------------
    State and local health departments..............             178              52             .45           4,165
                                                     ---------------------------------------------------------------
        Total.......................................  ..............  ..............  ..............           4,165
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        Dated: January 29, 1998.
    Wilma G. Johnson,
    Acting Associate Director for Policy Planning And Evaluation, Centers 
    for Disease Control and Prevention (CDC).
    [FR Doc. 98-2677 Filed 2-3-98; 8:45 am]
    BILLING CODE 4163-18-P
    
    
    

Document Information

Published:
02/04/1998
Department:
Centers for Disease Control and Prevention
Entry Type:
Notice
Document Number:
98-2677
Pages:
5806-5807 (2 pages)
Docket Numbers:
INFO-98-11
PDF File:
98-2677.pdf