Implementation of Newborn Screening for Conditions in the United States First Recommended during 2010–2018

Author:

Singh Sikha1,Ojodu Jelili1,Kemper Alex R.2,Lam Wendy K. K.3,Grosse Scott D.4ORCID

Affiliation:

1. Association of Public Health Laboratories, Silver Spring, MD 20910, USA

2. Division of Primary Care Pediatrics, Nationwide Children’s Hospital, Columbus, OH 43205, USA

3. Clinical and Translational Science Institute, Duke University School of Medicine, Durham, NC 27710, USA

4. National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA 30341, USA

Abstract

The Recommended Uniform Screening Panel (RUSP) is the list of conditions recommended by the US Secretary of Health and Human Services for inclusion in state newborn screening (NBS). During 2010–2022, seven conditions were added to the RUSP: severe combined immunodeficiency (SCID) (2010), critical congenital heart disease (CCHD) (2011), glycogen storage disease, type II (Pompe) (2015), mucopolysaccharidosis, type I (MPS I) (2016), X-linked adrenoleukodystrophy (X-ALD) (2016), spinal muscular atrophy (SMA) (2018), and mucopolysaccharidosis, type II (MPS II) (2022). The adoption of SCID and CCHD newborn screening by programs in all 50 states and three territories (Washington, D.C.; Guam; and Puerto Rico) took 8.6 and 6.8 years, respectively. As of December 2022, 37 programs screen for Pompe, 34 for MPS I, 32 for X-ALD, and 48 for SMA. The pace of implementation based on the average additional number of NBS programs per year was most rapid for SMA (11.3), followed by CCHD (7.8), SCID (6.2), MPS I (5.4), Pompe (4.9), and X-ALD (4.7).

Funder

US Department of Health and Human Services, Health Resources and Services Administration under Cooperative Agreement

Association of Public Health Laboratories and Contract

Duke University

Publisher

MDPI AG

Subject

Obstetrics and Gynecology,Immunology and Microbiology (miscellaneous),Pediatrics, Perinatology and Child Health

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