Literature DB >> 17183569

Changing perspectives on the benefits of newborn screening.

Donald B Bailey1, Laura M Beskow, Arlene M Davis, Debra Skinner.   

Abstract

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. Copyright (c) 2006 Wiley-Liss, Inc.

Mesh:

Year:  2006        PMID: 17183569     DOI: 10.1002/mrdd.20119

Source DB:  PubMed          Journal:  Ment Retard Dev Disabil Res Rev        ISSN: 1080-4013


  22 in total

1.  Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders.

Authors:  Yvonne Bombard; Fiona A Miller; Robin Z Hayeems; Brenda J Wilson; June C Carroll; Martha Paynter; Julian Little; Judith Allanson; Jessica P Bytautas; Pranesh Chakraborty
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

2.  Newborn screening for sickle cell disease: whose reproductive benefit?

Authors:  Lainie Friedman Ross
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

3.  Reply to Ross' commentary: Reproductive benefit through newborn screening: preferences, policy and ethics.

Authors:  Yvonne Bombard; Fiona A Miller
Journal:  Eur J Hum Genet       Date:  2012-02-29       Impact factor: 4.246

Review 4.  Potential Uses and Inherent Challenges of Using Genome-Scale Sequencing to Augment Current Newborn Screening.

Authors:  Jonathan S Berg; Cynthia M Powell
Journal:  Cold Spring Harb Perspect Med       Date:  2015-10-05       Impact factor: 6.915

5.  The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

Authors:  Yvonne Bombard; Fiona A Miller; Robin Z Hayeems; Denise Avard; Bartha M Knoppers; Martina C Cornel; Pascal Borry
Journal:  Nat Rev Genet       Date:  2009-10       Impact factor: 53.242

Review 6.  Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening.

Authors:  Yvonne Bombard; Fiona A Miller; Robin Z Hayeems; Denise Avard; Bartha M Knoppers
Journal:  Eur J Hum Genet       Date:  2010-03-03       Impact factor: 4.246

Review 7.  International differences in the evaluation of conditions for newborn bloodspot screening: a review of scientific literature and policy documents.

Authors:  Marleen E Jansen; Selina C Metternick-Jones; Karla J Lister
Journal:  Eur J Hum Genet       Date:  2016-11-16       Impact factor: 4.246

8.  Newborn screening and cascade testing for FMR1 mutations.

Authors:  Page L Sorensen; Louise W Gane; Mark Yarborough; Randi J Hagerman; Flora Tassone
Journal:  Am J Med Genet A       Date:  2012-12-13       Impact factor: 2.802

9.  Biobank participant support of newborn screening for disorders with variable treatment and intervention options.

Authors:  Megan E Bunnell; Beth A Tarini; Michael Petros; Aaron J Goldenberg; Aishwarya Arjunan; Catherine Wicklund
Journal:  J Community Genet       Date:  2016-09-01

10.  A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.

Authors:  Flora Tassone; Ruiqin Pan; Khaled Amiri; Annette K Taylor; Paul J Hagerman
Journal:  J Mol Diagn       Date:  2007-12-28       Impact factor: 5.568

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.