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    Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children

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    Authors
    Kemper, Alex R.
    Green, Nancy S.
    Calonge, Ned
    Lam, Wendy K.K.
    Comeau, Anne Marie
    Goldenberg, Aaron J.
    Ojodu, Jelili
    Prosser, Lisa A.
    Tanksley, Susan
    Bocchini, Joseph A. Jr.
    UMass Chan Affiliations
    New England Newborn Screening Program
    Department of Pediatrics
    Document Type
    Journal Article
    Publication Date
    2014-02-01
    Keywords
    *Advisory Committees
    Child
    Child, Preschool
    *Decision Making
    *Evidence-Based Medicine
    Humans
    Infant
    Infant, Newborn
    Neonatal Screening
    United States
    *United States Dept. of Health and Human Services
    Congenital, Hereditary, and Neonatal Diseases and Abnormalities
    Maternal and Child Health
    Medical Genetics
    Pediatrics
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    Link to Full Text
    http://dx.doi.org/10.1038/gim.2013.98
    Abstract
    PURPOSE: The US Secretary of Health and Human Services provides guidance to state newborn screening programs about which conditions should be included in screening (i.e., the "Recommended Uniform Screening Panel"). This guidance is informed by evidence-based recommendations from the Secretary's Advisory Committee on Heritable Disorders in Newborns and Children. This report describes the Advisory Committee's revised decision-making process for considering conditions nominated to the panel. METHODS: An expert panel meeting was held in April 2012 to revise the decision matrix, which helps to guide the recommendation process. In January 2013, the Advisory Committee voted to adopt the revised decision matrix. RESULTS: The revised decision matrix clarifies the approach to rating magnitude and certainty of the net benefit of screening to the population of screened newborns for nominated conditions, and now includes the consideration of the capability of state newborn screening programs for population-wide implementation by evaluating the feasibility and readiness of states to adopt screening for nominated conditions. CONCLUSION: The revised decision matrix will bring increased quality, transparency, and consistency to the process of modifying the recommended uniform screening panel and will now allow formal evaluation of the challenges that state newborn screening programs face in adopting screening for new conditions.
    Source
    Genet Med. 2014 Feb;16(2):183-7. doi: 10.1038/gim.2013.98. Epub 2013 Aug 1. Link to article on publisher's site
    DOI
    10.1038/gim.2013.98
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/30249
    PubMed ID
    23907646
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1038/gim.2013.98
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