Evidence map›Paper›PMID 38651397›Full record

ArticleInternational journal of neonatal screening2024

Assessing the Benefits and Harms Associated with Early Diagnosis from the Perspective of Parents with Multiple Children Diagnosed with Duchenne Muscular Dystrophy.

Oindrila Bhattacharyya, Nicola B Campoamor, Niki Armstrong, Megan Freed, Rachel Schrader, Norah L Crossnohere, John F P Bridges

Open access · goldAbstract read
In one paragraph

Article in International journal of neonatal screening, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 32% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Duchenne Muscular Dystrophy Under Three Years of Age.Children (Basel, Switzerland) · 2026
    Article
  2. Article
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

7 authors at 3 institutions in 1 country.

Oindrila BhattacharyyaDepartment of Biomedical Informatics, The Ohio State University College of Medicine, Columbus, OH 43210, USA.ORCID 0000-0001-9006-7409
Nicola B CampoamorDepartment of Biomedical Informatics, The Ohio State University College of Medicine, Columbus, OH 43210, USA.ORCID 0009-0005-7836-5135
Niki ArmstrongFoundation for Angelman Syndrome Therapeutics, Austin, TX 78704, USA.
Megan FreedParent Project Muscular Dystrophy, Washington, DC 20005, USA.
Rachel SchraderParent Project Muscular Dystrophy, Washington, DC 20005, USA.
Norah L CrossnohereDepartment of Internal Medicine, The Ohio State University College of Medicine, Columbus, OH 43202, USA.
John F P BridgesDepartment of Biomedical Informatics, The Ohio State University College of Medicine, Columbus, OH 43210, USA.
The Ohio State University · USParent Project Muscular Dystrophy · USRome Foundation · US

Funding

Burroughs Wellcome Fund No grant number availableParent Project Muscular Dystrophy No grant number available
6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is a rare neuromuscular disorder diagnosed in childhood. Limited newborn screening in the US often delays diagnosis. With multiple FDA-approved therapies, early diagnosis is crucial for timely treatment but may entail other benefits and harms. Using a community-based survey, we explored how parents of siblings with DMD perceived early diagnosis of one child due to a prior child's diagnosis. We assessed parents' viewpoints across domains including diagnostic journey, treatment initiatives, service access, preparedness, parenting, emotional impact, and caregiving experience. We analyzed closed-ended responses on a -1.0 to +1.0 scale to measure the degree of harm or benefit parents perceived and analyzed open-ended responses thematically. A total of 45 parents completed the survey, with an average age of 43.5 years and 20.0% identifying as non-white. Younger siblings were diagnosed 2 years earlier on average (

Indexed as

Duchenne muscular dystrophyearly diagnosisnewborn screening

Identifiers

PMID38651397
PMCPMC11036293
OpenAlexW4394822059

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.