Evidence map›Paper›PMID 39876584›Full record

ArticlePediatric pulmonology2025

Pulmonary Morbidity in Congenital Diaphragmatic Hernia Survivors Treated at a Non-ECMO Center From 1998 to 2015: A Cross-Sectional Study.

Ulla Lei Larsen, Lone Agertoft, Anne Maria Herskind, Thomas Strøm, Palle Toft, Susanne Halken

Abstract read
In one paragraph

Article in Pediatric pulmonology, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ulla Lei LarsenResearch Unit for Department of Anaesthesiology & Intensive Care, Odense University Hospital, Odense, Denmark.ORCID http://orcid.org/0000-0002-6986-2907
Lone AgertoftDepartment of Paediatrics, University Hospital of Southern Denmark, Aabenraa, Denmark.
Anne Maria HerskindH.C. Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
Thomas StrømResearch Unit for Department of Anaesthesiology & Intensive Care, Odense University Hospital, Odense, Denmark.
Palle ToftResearch Unit for Department of Anaesthesiology & Intensive Care, Odense University Hospital, Odense, Denmark.
Susanne HalkenDepartment of Clinical Research, Faculty of Health sciences, University of Southern Denmark, Odense, Denmark.

Funding

This study was supported by The Child Lung Foundation in Denmark (Børnelungefonden); Læge Else Poulsens Mindelegat (grant number 53-A2591); and DASAIMs Research initiative fond (Danske Selskab for Anæstesiologi og Intensiv Medicin). Also, through scholarships from The University of Southern Denmark (Syddansk Universitet) and The Research Council of the region of Southern Denmark (grant number 18/17564).
6 · The paper itself

Abstract

introductionA main feature of CDH is lung hypoplasia and the related presentation of pulmonary hypertension and cardiac dysfunction. Multiple factors influence pulmonary status after CDH: degree of hypoplasia, ventilator-induced injury, altered growth and development of pulmonary structures, reduced diaphragm function and chest wall abnormalities. The evolution of pulmonary sequela in this population is still unclear. We aimed to describe the pulmonary status of our population of CDH-survivors and evaluated on risk factors.

methodsCDH-survivors (1998-2015) were included and performed lung function tests and chest X-rays.

resultsFifty-one (51/71, 71.8%) participated. Median age was 12.2 (5.5-21.4) years, 28 (54.9%) male, 42 (82.4%) had left-sided hernias, 10 (19.6%) needed patch-repair and median length of stay in hospital was 28.0 (IQR 18.5-61.6) days in Table 1. Spirometry including bronchodilator response (BDR)-test, body plethysmography, and diffusion capacity, were available for 48, 42, and 40 participants. The mean (SD) z-score for FEV1 and FVC was -0.26 (1.70) and -0.28 (1.70). Twenty-one (43.8%) had obstructive patterns and six had positive BDR. TLC mean (SD) z-score was -0.18 (1.10). Four showed restricted/mixed patterns and 13 showed signs of hyperinflation. Increased RV/TLC-ratio and reduced FEV1 was associated with longer time on mechanical ventilation. Diffusion capacity was decreased in three cases. Chest X-ray revealed hernia recurrence (13.9%) and scoliosis (38.9%).

conclusionMild obstructive impairment and hyperinflation was frequent in our CDH cohort and only a small subset of restrictive disorders were identified. We advocate follow-up by a specialized multidisciplinary team through childhood and into adulthood.

Indexed as

Hernias, Diaphragmatic, CongenitalLungLung DiseasesAdolescentChildChild, PreschoolCross-Sectional StudiesFemaleHumansLength of StayMaleRespiratory Function TestsRisk FactorsSurvivorsYoung Adult

Identifiers

PMID39876584
PMCPMC11775427

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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.