Evidence map›Paper›PMID 39843779›Full record

ArticlePediatric research2025

Isolated congenital diaphragmatic hernia and three-year neurodevelopmental outcomes.

Katsuaki Toyoshima, Hirosato Aoki, Kaoru Katsumata, Yoshiaki Sato, Hirosuke Inoue, Miharu Ito, Shoichiro Amari, Hidehiko Maruyama, Hitomi Arahori, Takuya Kondo and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Pediatric research, 2025. 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

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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

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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.

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4 · The record

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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

18 authors.

Katsuaki ToyoshimaDepartment of Neonatology, Kanagawa Children's Medical Center, Yokohama, Japan. nqf37179@nifty.com.
Hirosato AokiDepartment of Neonatology, Kanagawa Children's Medical Center, Yokohama, Japan.
Kaoru KatsumataDepartment of Neonatology, Kanagawa Children's Medical Center, Yokohama, Japan.
Yoshiaki SatoDivision of Neonatology, Center for Maternal-Neonatal Care, Nagoya University Hospital, Nagoya, Japan.
Hirosuke InoueDepartment of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Miharu ItoDivision of Neonatology, Center for Maternal-Neonatal Care, Nagoya University Hospital, Nagoya, Japan.
Shoichiro AmariDivision of Neonatology, National Center for Child Health and Development, Tokyo, Japan.
Hidehiko MaruyamaDivision of Neonatology, National Center for Child Health and Development, Tokyo, Japan.
Hitomi ArahoriDepartment of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
Takuya KondoDepartment of Pediatric Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Kiyokazu KimDepartment of Pediatric Surgery, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Masaya YamotoDepartment of Pediatric Surgery, Shizuoka Children's Hospital, Shizuoka, Japan.
Tomoko SaitoDepartment of Neonatology, Kanagawa Children's Medical Center, Yokohama, Japan.
Hiroomi OkuyamaDepartment of Pediatric Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Noriaki UsuiDepartment of Pediatric Surgery, Osaka Women's and Children's Hospital, Osaka, Japan.
Keita TeruiDivision of Pediatric Surgery, Department of Surgery, Jichi Medical University, School of Medicine, Tochigi, Japan.
Kouji NagataDepartment of Pediatric Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Japanese Congenital Diaphragmatic Hernia Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo retrospectively investigate the developmental outcomes at 3 years of age in patients with congenital diaphragmatic hernia (CDH) using a multicenter collaborative research approach.

methodsWe evaluated patients with CDH and no other malformations born between 2010 and 2016 in seven facilities in the Japanese CDH Research Group. The developmental quotient (DQ) at 3 years of age was evaluated using the Kyoto Scale of Psychological Development 2001, the most standardized scale in Japan. Factors associated with a DQ score < 85 were also analyzed.

resultsOf 196 patients, developmental assessments at 3 years of age were performed in 132 patients (67%). Among these, 99 patients (75%) had a DQ score ≥ 85, 25 (19%) had a DQ score between 70 and 84, and 8 (6%) had a DQ score < 70. Multivariate analysis showed that the observed/expected lung area-to-head circumference ratio was an independent predictor of a DQ score < 85, with an adjusted odds ratio of 0.62 (95% confidence interval: 0.40-0.96; p = 0.03).

conclusionGenerally, isolated CDH is associated with good developmental outcomes for survivors, even after intensive care. However, there is a risk of neurodevelopmental impairment if pulmonary hypoplasia is present. IMPACT: This research highlights the observed/expected lung area-to-head circumference ratio (o/e LHR) as a crucial indicator to predict neurodevelopmental outcomes in 3-year-old children diagnosed with isolated congenital diaphragmatic hernia (CDH). Our results provide robust evidence from a large multicenter cohort, emphasizing the importance of o/e LHR in early risk stratification and prolonged neurodevelopmental follow-up. These findings highlight the need for comprehensive management and tailored follow-up care in CDH patients, potentially improving clinical protocols and enhancing the quality of life and outcomes for affected children.

Indexed as

Child DevelopmentHernias, Diaphragmatic, CongenitalNeurodevelopmental DisordersChild, PreschoolDevelopmental DisabilitiesFemaleHumansJapanLungMaleRetrospective Studies

Identifiers

PMID39843779
PMCPMC12454112

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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.