3.8 Review

Changing perspectives on the benefits of newborn screening

Publisher

WILEY-LISS
DOI: 10.1002/mrdd.20119

Keywords

consumer advocacy; early intervention; family; infant; newborn; newborn screening

Funding

  1. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT [R21HD043616] Funding Source: NIH RePORTER
  2. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [P20HG003387] Funding Source: NIH RePORTER
  3. NHGRI NIH HHS [P20-HG003387] Funding Source: Medline
  4. NICHD NIH HHS [R21-HD043616] Funding Source: Medline

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The likelihood of benefit is fundamental to decision making about newborn screening. But benefit is construed in different ways by different stakeholders. This article begins with a review of benefit as considered historically by various expert panels and organizations. We then show how 78 conditions fared when experts recently rated them on benefit using a scoring system recommended by a task force of the American College of Medical Genetics. Finally, we analyze how benefit is reflected in the public comments submitted in response to the ACMG report. Results show that benefit has been and remains a core consideration for screening decisions. Historically the focus has been on improved physical health as a result of medical treatment; however, in only 4 of the 78 conditions rated does newborn screening prevent all negative consequences. In fact the majority of both core conditions (51.7%) and secondary targets (87.5%) recommended in the ACMG report were rated as having treatments that prevented only some negative consequences. All conditions rated had perceived benefits for family and society, but currently no conditions are screened on the basis of family or societal benefits alone. No agreed-upon threshold exists for what would be considered meaningful benefit, and stakeholder groups differ in their perceptions of benefit. We conclude by suggesting several key research studies needed to further inform public policy. (c) 2006 Wiley-Liss, Inc.

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