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Guidelines for implementation of population-based newborn screening for severe combined immunodeficiency
Authors:Anne Marie Comeau  Jaime E. Hale  Sung-Yun Pai  Francisco A. Bonilla  Luigi D. Notarangelo  Mark S. Pasternack  H. Cody Meissner  Ellen Rae Cooper  Alfred DeMaria  Inderneel Sahai  Roger B. Eaton
Affiliation:1.New England Newborn Screening Program,UMass Medical School,Jamaica Plain,USA;2.Children’s Hospital,Boston,USA;3.Dana-Farber Cancer Institute,Boston,USA;4.Massachusetts General Hospital,Boston,USA;5.Tufts Medical Center,Boston,USA;6.Boston Medical Center,Boston,USA;7.Massachusetts Department of Public Health,Boston,USA
Abstract:Severe combined immunodeficiency (SCID) is a Primary Immune Deficiency that is under consideration for population-based newborn screening (NBS) by many NBS programs, and has recently been recommended for inclusion in the US uniform panel of newborn screening conditions. A marker of SCID, the T cell receptor excision circle (TREC), is detectable in the newborn dried blood spot using a unique molecular assay as a primary screen. The New England Newborn Screening Program developed and validated a multiplex TREC assay in which both the TREC analyte and an internal control are acquired from a single punch and run in the same reaction. Massachusetts then implemented a statewide pilot SCID NBS program. The authors describe the rationale for a pilot SCID NBS program, a comprehensive strategy for successful implementation, the screening test algorithm, the screening follow-up algorithm and preliminary experience based on statewide screening in the first year. The Massachusetts experience demonstrates that SCID NBS is a program that can be implemented on a population basis with reasonable rates of false positives.
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