Evidence map›Paper›PMID 39994065›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2025

Posterior vault encephaloceles: from antenatal management to post-surgical follow-up-a cooperative study.

Claudia Pasquali, Ulrich-Wilhelm Thomale, Alexandru Szathamri, Pier Aurelien Beuriat, Valentina Pennacchietti, Mélodie Anne Karnoub, Matthieu Vinchon, Federico Di Rocco

Erratum issuedAbstract readMulticenter Study
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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.

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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Claudia PasqualiHôpital Femme Mère Enfant, Université de Lyon, INSERM 1033, Lyon, France.
Ulrich-Wilhelm ThomalePediatric Neurosurgery Charité - Universitätsmedizin, Berlin, Germany.
Alexandru SzathamriHôpital Femme Mère Enfant, Université de Lyon, INSERM 1033, Lyon, France.
Pier Aurelien BeuriatHôpital Femme Mère Enfant, Université de Lyon, INSERM 1033, Lyon, France.
Valentina PennacchiettiPediatric Neurosurgery Charité - Universitätsmedizin, Berlin, Germany.
Mélodie Anne KarnoubPediatric Neurosurgery Hôpital Roger Salengro, Lille, France.
Matthieu VinchonHôpital Femme Mère Enfant, Université de Lyon, INSERM 1033, Lyon, France.
Federico Di RoccoHôpital Femme Mère Enfant, Université de Lyon, INSERM 1033, Lyon, France. federico.dirocco@chu-lyon.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEncephalocele is a herniation of intracranial structures associated with a skull anomaly. In Western countries, posterior encephaloceles are more common than anterior encephaloceles and may occur in the parietal (parietal encephalocele, PE) or occipital (occipital encephalocele, OE) region. Although those entities are relatively common in pediatric neurosurgery, large clinical series are scarce, and their clinical outcomes are poorly documented in the literature.

methodsWe retrospectively analyzed the clinical and radiological findings, post-operative long-term outcomes of consecutive patients diagnosed with posterior encephaloceles from 2010 to 2021 in 3 centers: Hôpital Femme Mère Enfant (Lyon, France); Hôpital Roger Salengro (Lille, France); and Charité Universitätsmedizin (Berlin, Germany).

resultsWe collected 79 observations, 46 PEs and 33 OEs. Cerebral anomalies were more common in OEs than PEs (15/33, 45% vs 7/46, 15%, p = 0.001). Vascular anomalies were more common in PEs than OEs (41/46, 88% vs 5/33, 15%). All children underwent a surgical correction of the malformation. CSF disorders requiring surgical management were present in 4/33 OEs and 4/46 PEs. During the mean follow-up of 33 months (12-160 months), 3 OEs patients died, and various degrees of psychomotor impairment were found in both entities: 18/33 (54%) OEs and 8/46 (17%) PEs (p = 0.005); however, in most cases of PE, developmental delay was mild.

conclusionsThe clinical evolution in OEs is significantly more unfavorable than in PEs. However, even in case of PEs, psychomotor impairments are not uncommon. The presence of herniated cerebral tissue, hydrocephalus, and syndromic context increase the risk of developmental delay.

Indexed as

EncephaloceleChildChild, PreschoolDisease ManagementFemaleFollow-Up StudiesHumansInfantInfant, NewbornMaleNeurosurgical ProceduresPregnancyRetrospective StudiesTreatment OutcomeAtretic cephaloceleCerebral malformationsDevelopmental outcomeOccipital meningocelePrenatal diagnosis

Identifiers

PMID39994065
PMCPMC11850399

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.