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ScreenPlus: A comprehensive, multi-disorder newborn screening program.
Kelly, Nicole R; Orsini, Joseph J; Goldenberg, Aaron J; Mulrooney, Niamh S; Boychuk, Natalie A; Clarke, Megan J; Paleologos, Katrina; Martin, Monica M; McNeight, Hannah; Caggana, Michele; Bailey, Sean M; Eiland, Lisa R; Ganesh, Jaya; Kupchik, Gabriel; Lumba, Rishi; Nafday, Suhas; Stroustrup, Annemarie; Gelb, Michael H; Wasserstein, Melissa P.
Afiliação
  • Kelly NR; Department of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
  • Orsini JJ; Newborn Screening Program, Wadsworth Center, New York State Department of Health, Albany, 12208, NY, USA.
  • Goldenberg AJ; Department of Bioethics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
  • Mulrooney NS; Department of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
  • Boychuk NA; Touro College of Osteopathic Medicine, New York, NY 10027, USA.
  • Clarke MJ; Department of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
  • Paleologos K; Department of Epidemiology, Columbia University Mailman School of Public Health, New York, NY 10032, USA.
  • Martin MM; Department of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
  • McNeight H; Department of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
  • Caggana M; Newborn Screening Program, Wadsworth Center, New York State Department of Health, Albany, 12208, NY, USA.
  • Bailey SM; Division of Health and Safety-Compliance, New York State Office of Cannabis Management, Albany, NY 12226, USA.
  • Eiland LR; Newborn Screening Program, Wadsworth Center, New York State Department of Health, Albany, 12208, NY, USA.
  • Ganesh J; Newborn Screening Program, Wadsworth Center, New York State Department of Health, Albany, 12208, NY, USA.
  • Kupchik G; Division of Neonatology, NYU Grossman School of Medicine, New York, NY 10016, USA.
  • Lumba R; Division of Newborn Medicine and Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Nafday S; Division of Neonatology, Hackensack University Medical Center, Joseph M. Sanzari Children's Hospital, Hackensack, NJ 07601, USA.
  • Stroustrup A; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Gelb MH; Division of Medical Genetics, Maimonides Children's Hospital of Brooklyn, Brooklyn, NY 11219, USA.
  • Wasserstein MP; Division of Neonatology, NYU Grossman School of Medicine, New York, NY 10016, USA.
Mol Genet Metab Rep ; 38: 101037, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38173711
ABSTRACT
The increasing availability of novel therapies highlights the importance of screening newborns for rare genetic disorders so that they may benefit from early therapy, when it is most likely to be effective. Pilot newborn screening (NBS) studies are a way to gather objective evidence about the feasibility and utility of screening, the accuracy of screening assays, and the incidence of disease. They are also an optimal way to evaluate the complex ethical, legal and social implications (ELSI) that accompany NBS expansion for disorders. ScreenPlus is a consented pilot NBS program that aims to enroll over 100,000 infants across New York City. The initial ScreenPlus panel includes 14 disorders and uses an analyte-based, multi-tiered screening platform in an effort to enhance screening accuracy. Infants who receive an abnormal result are referred to a ScreenPlus provider for confirmatory testing, management, and therapy as needed, along with longitudinal capture of outcome data. Participation in ScreenPlus requires parental consent, which is obtained in active and passive manners. Patient-facing documents are translated into the ten most common languages spoken at our nine pilot hospitals, all of which serve diverse communities. At the time of consent, parents are invited to receive a series of online surveys to capture their opinions about specific ELSI-related topics, such as NBS policy, residual dried blood spot retention, and the types of disorders that should be on NBS panels. ScreenPlus has developed a stakeholder-based, collective funding model that includes federal support in addition to funding from 14 advocacy and industry sponsors, all of which have a particular interest in NBS for at least one of the ScreenPlus disorders. Taken together, ScreenPlus is a model, multi-sponsored pilot NBS program that will provide critical data about NBS for a broad panel of disorders, while gathering key stakeholder opinions to help guide ethically sensitive decision-making about NBS expansion.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies / Qualitative_research / Screening_studies Idioma: En Revista: Mol Genet Metab Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies / Qualitative_research / Screening_studies Idioma: En Revista: Mol Genet Metab Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos