Evidence map›Paper›PMID 38173711›Full record

ArticleMolecular genetics and metabolism reports2024

ScreenPlus: A comprehensive, multi-disorder newborn screening program.

Nicole R Kelly, Joseph J Orsini, Aaron J Goldenberg, Niamh S Mulrooney, Natalie A Boychuk, Megan J Clarke, Katrina Paleologos, Monica M Martin, Hannah McNeight, Michele Caggana and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05368038 (ScreenPlus), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05368038 enrolling by invitationnot on this map

ScreenPlus: A Comprehensive, Flexible, Multi-disorder Newborn Screening Program

TypeobservationalSponsorAlbert Einstein College of MedicineRan2021 to 2029Enrolled100,000ConditionsAcid Sphingomyelinase Deficiency, Ceroid Lipofuscinosis, Neuronal, 2, Cerebrotendinous Xanthomatosis, Fabry DiseaseArmsConfirmatory Testing
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 13 institutions in 1 country.

Nicole R KellyDepartment of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
Joseph J OrsiniNewborn Screening Program, Wadsworth Center, New York State Department of Health, Albany, 12208, NY, USA.
Aaron J GoldenbergDepartment of Bioethics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Niamh S MulrooneyDepartment of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
Natalie A BoychukDepartment of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
Megan J ClarkeDepartment of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
Katrina PaleologosDepartment of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
Monica M MartinNewborn Screening Program, Wadsworth Center, New York State Department of Health, Albany, 12208, NY, USA.
Hannah McNeightNewborn Screening Program, Wadsworth Center, New York State Department of Health, Albany, 12208, NY, USA.
Michele CagganaNewborn Screening Program, Wadsworth Center, New York State Department of Health, Albany, 12208, NY, USA.
Sean M BaileyDivision of Neonatology, NYU Grossman School of Medicine, New York, NY 10016, USA.
Lisa R EilandDivision of Newborn Medicine and Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Jaya GaneshDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Gabriel KupchikDivision of Medical Genetics, Maimonides Children's Hospital of Brooklyn, Brooklyn, NY 11219, USA.
Rishi LumbaDivision of Neonatology, NYU Grossman School of Medicine, New York, NY 10016, USA.
Suhas NafdayDepartment of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
Annemarie StroustrupDivision of Neonatal Services, Cohen Children's Medical Center, New Hyde Park, NY 11040, USA.
Michael H GelbDepartment of Chemistry and Biochemistry, University of Washington, Seattle, WA 98195, USA.
Melissa P WassersteinDepartment of Pediatrics, Albert Einstein College of Medicine and Children's Hospital at Montefiore, Bronx, NY 10467, USA.
Albert Einstein College of Medicine · USNew York State Department of Health · USNew York University · USWadsworth Center · USCase Western Reserve University · USChildren's Hospital at Montefiore · USCohen Children's Medical Center · USColumbia University · USHackensack University Medical Center · USIcahn School of Medicine at Mount Sinai · USMaimonides Medical Center · USTouro College · USUniversity of Washington · US

Funding

NY ScreenPlus: A Comprehensive, Flexible, Multi-disorder Newborn Screening ProgramR01HD073292 · NICHD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Melissa Pittel Wasserstein · 2012 to 2026
$8.3M
NICHD NIH HHS R01 HD073292
6 · The paper itself

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.

Indexed as

ELSIEthicsExpanded conditionsNewborn screeningPilot studiesResearch

Identifiers

PMID38173711
PMCPMC10761901
OpenAlexW4389763763

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.