Actions in Support of Newborn Screening for Critical Congenital Heart Disease — United States, 2011–2018

Author:

Glidewell Jill,Grosse Scott D.,Riehle-Colarusso Tiffany,Pinto Nelangi,Hudson Jeff,Daskalov Rachel,Gaviglio Amy,Darby Erin,Singh Sikha,Sontag Marci

Publisher

Centers for Disease Control MMWR Office

Subject

Health Information Management,Health, Toxicology and Mutagenesis,General Medicine,Health(social science),Epidemiology

Reference10 articles.

1. US Department of Health and Human Services Office of the Secretary. Letter from the Secretary to the Advisory Committee on Heritable Disorders in Newborns and Children, September 21, 2011. Washington, DC: US Department of Health and Human Services; 2011. https://www.hrsa.gov/sites/default/files/hrsa/advisory-committees/heritable-disorders/reports-recommendations/response-congenital-cyanotic.pdf

2. Role of pulse oximetry in examining newborns for congenital heart disease: a scientific statement from the AHA and AAP.;Mahle;Pediatrics,2009

3. Association of US state implementation of newborn screening policies for critical congenital heart disease with early infant cardiac deaths.;Abouk;JAMA,2017

4. State legislation, regulations, and hospital guidelines for newborn screening for critical congenital heart defects—United States, 2011–2014.;Glidewell;MMWR Morb Mortal Wkly Rep,2015

5. CDC grand rounds: newborn screening for hearing loss and critical congenital heart disease.;Grosse;MMWR Morb Mortal Wkly Rep,2017

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