Literature DB >> 21716119

What questions should newborn screening long-term follow-up be able to answer? A statement of the US Secretary for Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children.

Cynthia F Hinton1, Lisa Feuchtbaum, Christopher A Kus, Alex R Kemper, Susan A Berry, Jill Levy-Fisch, Julie Luedtke, Celia Kaye, Coleen A Boyle.   

Abstract

The US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children provides guidance on reducing the morbidity and mortality associated with heritable disorders detectable through newborn screening. Efforts to systematically evaluate health outcomes, beyond long-term survival, with a few exceptions, are just beginning. To facilitate these nascent efforts, the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children initiated a project to define the major overarching questions to be answered to assure that newborn screening is meeting its goal of achieving the best quality outcome for the affected children and their families. The questions identified follow the central components of long-term follow-up-care coordination, evidence-based treatment, continuous quality improvement, and new knowledge discovery-and are framed from the perspectives of the state and nation, primary and specialty healthcare providers, and the impacted families. These overarching questions should be used to guide the development of long-term follow-up data systems, quality health indicators, and specific data elements for evaluating the newborn screening system.

Entities:  

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Year:  2011        PMID: 21716119     DOI: 10.1097/GIM.0b013e3182209f09

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


  11 in total

1.  Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2. From screening laboratory results to treatment, follow-up and quality assurance.

Authors:  Peter Burgard; Kathrin Rupp; Martin Lindner; Gisela Haege; Tessel Rigter; Stephanie S Weinreich; J Gerard Loeber; Domenica Taruscio; Luciano Vittozzi; Martina C Cornel; Georg F Hoffmann
Journal:  J Inherit Metab Dis       Date:  2012-04-28       Impact factor: 4.982

2.  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 3.  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

4.  Clinical Follow-Up for Duchenne Muscular Dystrophy Newborn Screening: A Proposal.

Authors:  Jennifer M Kwon; Hoda Z Abdel-Hamid; Samiah A Al-Zaidy; Jerry R Mendell; Annie Kennedy; Kathi Kinnett; Valerie A Cwik; Natalie Street; Julie Bolen; John W Day; Anne M Connolly
Journal:  Muscle Nerve       Date:  2016-06-13       Impact factor: 3.217

5.  Primary Care Provider Management of Congenital Hypothyroidism Identified Through Newborn Screening.

Authors:  N A Rosenthal; E Bezar; S Mann; L K Bachrach; S Banerjee; M E Geffner; M Gottschalk; S K Shapira; L Hasegawa; L Feuchtbaum
Journal:  Ann Thyroid Res       Date:  2017-04-18

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

Review 7.  Neonatal neuroimaging findings in inborn errors of metabolism.

Authors:  Andrea Poretti; Susan I Blaser; Maarten H Lequin; Ali Fatemi; Avner Meoded; Frances J Northington; Eugen Boltshauser; Thierry A G M Huisman
Journal:  J Magn Reson Imaging       Date:  2012-05-07       Impact factor: 4.813

8.  Empowering newborn screening programs in African countries through establishment of an international collaborative effort.

Authors:  Bradford L Therrell; Michele A Lloyd-Puryear; Kwaku Ohene-Frempong; Russell E Ware; Carmencita D Padilla; Emmanuela E Ambrose; Amina Barkat; Hassan Ghazal; Charles Kiyaga; Tisungane Mvalo; Obiageli Nnodu; Karim Ouldim; Mohamed Chérif Rahimy; Brígida Santos; Léon Tshilolo; Careema Yusuf; Guisou Zarbalian; Michael S Watson
Journal:  J Community Genet       Date:  2020-05-15

9.  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

10.  Infrastructure and Educational Needs of Newborn Screening Short-Term Follow-Up Programs within the Southeast Regional Newborn Screening & Genetics Collaborative: A Pilot Survey.

Authors:  Cecelia A Bellcross; Lokie Harmond; Phaidra Floyd-Browning; Rani Singh
Journal:  Healthcare (Basel)       Date:  2015-10-15
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