Expanding Newborn Screening for Pompe Disease in the United States: The NewSTEPs New Disorders Implementation Project, a Resource for New Disorder Implementation
- PMID: 33073038
- PMCID: PMC7423006
- DOI: 10.3390/ijns6020048
Expanding Newborn Screening for Pompe Disease in the United States: The NewSTEPs New Disorders Implementation Project, a Resource for New Disorder Implementation
Abstract
Public health programs in the United States screen more than four million babies each year for at least 30 genetic disorders. The Health and Human Services (HHS) Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC) recommends the disorders for state newborn screening (NBS) programs to screen. ACHDNC updated the Recommended Uniform Screening Panel (RUSP) to include Pompe disease in March 2015. To support the expansion of screening for Pompe disease, the Association of Public Health Laboratories (APHL) proposed the Newborn Screening Technical assistance and Evaluation Program (NewSTEPs) New Disorders Implementation Project, funded by the HHS' Health Resources and Services Administration (HRSA) Maternal and Child Health Bureau (MCHB). Through this project, APHL provided financial support to 15 state NBS programs to enable full implementation of screening for Pompe disease. As of April 27, 2020, nine of the 15 programs had fully implemented Pompe disease newborn screening and six programs are currently pursuing implementation. This article will discuss how states advanced to statewide implementation of screening for Pompe disease, the challenges associated with implementing screening for this condition, the lessons learned during the project, and recommendations for implementing screening for Pompe disease.
Keywords: Pompe disease; new disorders implementation; newborn screening.
© 2020 by the authors.
Conflict of interest statement
Conflicts of InterestThe authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of the data; in the writing of the manuscript, or in the decision to publish the results.
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References
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- Health Resources and Services Administration Advisory Committee on Heritable Disorders in Newborns and Children. [(accessed on 7 May 2020)]; Available online: https://www.hrsa.gov/advisory-committees/heritable-disorders/index.html.
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- Health Resources and Services Administration Recommended Uniform Screening Panel. [(accessed on 7 May 2020)]; Available online: https://www.hrsa.gov/advisory-committees/heritable-disorders/rusp/index.....
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- National Institutes of Health. U.S. National Library of Medicine Pompe Disease. [(accessed on 26 November 2019)]; Available online: https://ghr.nlm.nih.gov/condition/pompe-disease.
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- APHL Request for Proposals (RFP): Support for Newborn Screening Implementation of New RUSP Disorders. [(accessed on 7 May 2020)]; Available online: https://www.aphl.org/rfp/Documents/2017_RFP_Y02%20_New_Disorders_Project....
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