Evidence map›Paper›PMID 39912339›Full record

ArticleActa paediatrica (Oslo, Norway : 1992)2025

Infants With a Congenital Diaphragmatic Hernia Had Favourable Pulmonary Hypertension Outcomes at 1 Year of Age.

Alice Dirickx, Marilyne Levy, Kelly Mellul, Maxime Coignard, Naziha Khen-Dunlop, Alexandre Lapillonne, Julien Stirnemann, Elsa Kermorvant-Duchemin

Abstract read
In one paragraph

Article in Acta paediatrica (Oslo, Norway : 1992), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

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2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Alice DirickxDepartment of Neonatal Medicine, AP-HP, Necker-Enfants Malades Hospital, Paris, France.ORCID 0009-0001-2512-6887
Marilyne LevyDepartment of Pediatric Cardiology, AP-HP, Necker-Enfants Malades Hospital, Paris, France.
Kelly MellulDepartment of Neonatal Medicine, AP-HP, Necker-Enfants Malades Hospital, Paris, France.
Maxime CoignardDepartment of Neonatal Medicine, AP-HP, Necker-Enfants Malades Hospital, Paris, France.
Naziha Khen-DunlopDepartment of Pediatric Surgery, AP-HP, Necker Enfants-Malades Hospital, Paris, France.
Alexandre LapillonneDepartment of Neonatal Medicine, AP-HP, Necker-Enfants Malades Hospital, Paris, France.
Julien StirnemannUniversité Paris Cité, Paris, France.
Elsa Kermorvant-DucheminDepartment of Neonatal Medicine, AP-HP, Necker-Enfants Malades Hospital, Paris, France.

Funding

Fondation Université Paris Cité
6 · The paper itself

Abstract

aimPulmonary hypertension is frequent in neonates with a congenital diaphragmatic hernia, but long-term data have been scarce. Our aim was to examine its prevalence, evolution and management and identify factors associated with its persistence.

methodsThis French retrospective cohort study compared the characteristics of neonates who had persistent pulmonary hypertension, or died with it, and those with normalised pulmonary pressures at 1 month and 1 year of age.

resultsMost (92%) of the 88 neonates we studied underwent surgery. Two-thirds (67%) had preoperative pulmonary hypertension and they included 10 of the 11 who died after surgery. Pulmonary hypertension resolved after a median of 31 days in the 70 who were discharged alive and 27% required prolonged sildenafil treatment. At 1 year, 6 (9%) of the 65 children with echocardiographic data available still had elevated pulmonary pressures. Preoperative pulmonary hypertension, associated malformations and longer invasive ventilation were independently associated with persistent pulmonary hypertension at 1 month. Only prolonged invasive ventilation remained significant at 1 year.

conclusionDespite its high initial prevalence and impact on mortality, pulmonary hypertension resolved within weeks of surgery in the surviving neonates. The duration of invasive ventilation may have been a key factor in its persistence.

Indexed as

Hernias, Diaphragmatic, CongenitalHypertension, PulmonaryFemaleFranceHumansInfantInfant, NewbornMalePrevalenceRetrospective StudiesTreatment Outcomecongenital diaphragmatic herniafoetal tracheal occlusionpulmonary hypertensionsildenafil

Identifiers

PMID39912339
PMCPMC12147414

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