Literature DB >> 16980812

Exploring barriers to long-term follow-up in newborn screening programs.

Timothy Hoff1, Adrienne Hoyt, Brad Therrell, Maria Ayoob.   

Abstract

PURPOSE: To inform current policy debate regarding the public health role in long-term follow-up for individuals with disorders identified through state newborn testing efforts, by identifying and assessing key challenges, quality assurance activities, and long-term follow-up perceptions of state newborn screening programs.
METHODS: A 23-question, web-based survey sent to newborn screening programs in all 50 states and Washington, DC, during January and February, 2005.
RESULTS: Many U.S. newborn screening programs do not currently engage in structured long-term follow-up for newborns with diagnosed disorders. The newborn screening programs that do long-term follow-up face various challenges that may impact their ability to perform it effectively. Barriers include a lack of comprehensive quality assurance practices, outsourcing, financial constraints, and perceived communication problems with providers who treat these patients.
CONCLUSIONS: A more in-depth analysis of the desired and feasible roles that should be played by newborn screening programs in long-term follow-up is needed. The wide variability within programs regarding the structure and implementation of long-term follow-up, and the relative absence of long-term follow-up systems components in some newborn screening programs, poses an interesting question regarding responsibility for evaluation of longer-term outcomes associated with newborn testing and disorder diagnosis.

Entities:  

Mesh:

Year:  2006        PMID: 16980812     DOI: 10.1097/01.gim.0000237790.54074.3d

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  8 in total

1.  Quality performance of newborn screening systems: strategies for improvement.

Authors:  D Webster
Journal:  J Inherit Metab Dis       Date:  2007-08-14       Impact factor: 4.982

2.  Supporting family adaptation to presymptomatic and "untreatable" conditions in an era of expanded newborn screening.

Authors:  Donald B Bailey; F Daniel Armstrong; Alex R Kemper; Debra Skinner; Steven F Warren
Journal:  J Pediatr Psychol       Date:  2008-03-30

3.  Transient hypothyroidism at 3-year follow-up among cases of congenital hypothyroidism detected by newborn screening.

Authors:  Steven J Korzeniewski; Violanda Grigorescu; Mary Kleyn; William I Young; Gretchen Birbeck; David Todem; Roberto Romero; Nigel Paneth
Journal:  J Pediatr       Date:  2012-08-09       Impact factor: 4.406

Review 4.  Emerging issues in public health genomics.

Authors:  Dana Dolinoy; Beth Tarini; J Scott Roberts
Journal:  Annu Rev Genomics Hum Genet       Date:  2014       Impact factor: 8.929

5.  Tracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States-lessons learned.

Authors:  Judith Livingston; Bradford L Therrell; Marie Y Mann; Carolyn Stady Anderson; Katherine Christensen; Jerome L Gorski; Dorothy K Grange; Dawn Peck; Margy Roberston; Sharmini Rogers; Maura Taylor; Celia I Kaye
Journal:  J Community Genet       Date:  2011-07-06

6.  A framework for assessing outcomes from newborn screening: on the road to measuring its promise.

Authors:  Cynthia F Hinton; Charles J Homer; Alexis A Thompson; Andrea Williams; Kathryn L Hassell; Lisa Feuchtbaum; Susan A Berry; Anne Marie Comeau; Bradford L Therrell; Amy Brower; Katharine B Harris; Christine Brown; Jana Monaco; Robert J Ostrander; Alan E Zuckerman; Celia Kaye; Denise Dougherty; Carol Greene; Nancy S Green
Journal:  Mol Genet Metab       Date:  2016-05-31       Impact factor: 4.797

7.  Structures for clinical follow-up: newborn screening.

Authors:  R Rodney Howell; Gilian Engelson
Journal:  J Inherit Metab Dis       Date:  2007-08-10       Impact factor: 4.982

8.  Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings.

Authors:  Cynthia F Hinton; Cara T Mai; Sarah K Nabukera; Lorenzo D Botto; Lisa Feuchtbaum; Paul A Romitti; Ying Wang; Kimberly Noble Piper; Richard S Olney
Journal:  Genet Med       Date:  2013-12-05       Impact factor: 8.822

  8 in total

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