Evidence map›Paper›PMID 41854015›Full record

ArticleJournal of pediatric gastroenterology and nutrition2026

Neurodevelopmental assessment at 24 months in infants with esophageal atresia: A prospective cohort study.

Julia Tagmouti, Manon Midavaine, Victor Sartorius, Nicolas Vinit, Elise Leroy-Terquem, Sylvie Beaudoin, Elsa Kermorvant-Duchemin, Véronique Rousseau, Alexandre Lapillonne

Abstract read
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Article in Journal of pediatric gastroenterology and nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Julia TagmoutiDepartment of Neonatology and CRMR CRACMO, APHP, Necker-Enfants Malades University Hospital, Paris, France.ORCID https://orcid.org/0009-0000-1691-9212
Manon MidavaineDepartment of Neonatology and CRMR CRACMO, APHP, Necker-Enfants Malades University Hospital, Paris, France.
Victor SartoriusDepartment of Neonatology and CRMR CRACMO, APHP, Necker-Enfants Malades University Hospital, Paris, France.
Nicolas VinitUFR de Médecine, Paris Cité University, Paris, France.
Elise Leroy-TerquemDepartment of Neonatology and CRMR CRACMO, APHP, Necker-Enfants Malades University Hospital, Paris, France.
Sylvie BeaudoinUFR de Médecine, Paris Cité University, Paris, France.
Elsa Kermorvant-DucheminDepartment of Neonatology and CRMR CRACMO, APHP, Necker-Enfants Malades University Hospital, Paris, France.
Véronique RousseauDepartment of Pediatric Surgery, Urology and Transplantation, Necker-Enfants Malades University Hospital, APHP, Paris, France.
Alexandre LapillonneDepartment of Neonatology and CRMR CRACMO, APHP, Necker-Enfants Malades University Hospital, Paris, France.

Funding

ARFENNone
6 · The paper itself

Abstract

objectiveTo evaluate neurodevelopment at 24 months in infants surgically treated for esophageal atresia (EA), using the ages and stages questionnaire (ASQ), and identify perinatal and early-life factors associated with developmental delay.

methodsInfants with EA were prospectively enrolled in a structured multidisciplinary follow-up program. Total ASQ scores ≤185 were considered indicative of significant neurodevelopmental delay, while scores >220 reflected reassuring neurodevelopment. Five skill domains (communication, gross motor skills, fine motor skills, problem solving, and social skills) were also assessed. Clinical, surgical, and growth data were analyzed to identify associated risk factors.

resultsOf the 74 infants included, 13 patients (18%) had an ASQ score ≤185. Lower ASQ scores were significantly associated with prematurity, prolonged hospitalization, multiple surgeries, poor weight gain at 1 and 2 years, and feeding disorders. After adjusting for gestational age and genetic anomalies, prolonged hospitalization remained associated with lower ASQ scores, and higher weight-for-age at 1 and 2 years with better ASQ scores. Communication and social skills were the most severely affected, with approximately 80% of infants in the ASQ ≤ 185 group scoring below -2 standard deviations.

conclusionAlthough most children with EA demonstrated normal development at 2 years, a minority experienced significant delays, especially in communication and social skills. Early screening and targeted multidisciplinary follow-up are essential to support optimal outcomes in this high-risk population.

Indexed as

Child DevelopmentDevelopmental DisabilitiesEsophageal AtresiaNeurodevelopmentChild, PreschoolFemaleFollow-Up StudiesHumansInfantInfant, NewbornMaleProspective StudiesRisk FactorsSurveys and Questionnairescongenital gastrointestinal malformationsfeeding disordersneonatal surgeryneurodevelopment disordersperinatal factors

Identifiers

PMID41854015
PMCPMC13238391

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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.