Evidence map›Paper›PMID 40237858›Full record

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

Detailed analysis of hydrocephalus patterns and associated variables in patients after open fetal repair and postnatal myelomeningocele/myeloschisis closure.

Adam J Kundishora, Kamila Bond, Martin Rosenfeld, Sierra D Land, Taryn Gallagher, Tom A Reynolds, Juliana S Gebb, N Scott Adzick, Tracy M Flanders, Gregory G Heuer

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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. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Adam J KundishoraDivision of Neurosurgery, Department of Surgery, Children's Hospital of Philadelphia, 3501 Civic Center Boulevard, 10 th Floor, Hub for Clinical Collaboration, Philadelphia, PA, USA. kundishora@CHOP.edu.
Kamila BondDepartment of Neurosurgery, University of Pennsylvania Perlman School of Medicine, Philadelphia, PA, USA.
Martin RosenfeldDivision of Neurosurgery, Department of Surgery, Children's Hospital of Philadelphia, 3501 Civic Center Boulevard, 10 th Floor, Hub for Clinical Collaboration, Philadelphia, PA, USA.
Sierra D LandRichard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Taryn GallagherRichard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Tom A ReynoldsRichard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Juliana S GebbRichard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
N Scott AdzickRichard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Tracy M FlandersDivision of Neurosurgery, Department of Surgery, Children's Hospital of Philadelphia, 3501 Civic Center Boulevard, 10 th Floor, Hub for Clinical Collaboration, Philadelphia, PA, USA.
Gregory G HeuerDivision of Neurosurgery, Department of Surgery, Children's Hospital of Philadelphia, 3501 Civic Center Boulevard, 10 th Floor, Hub for Clinical Collaboration, Philadelphia, PA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyelomeningocele (MMC) and myeloschisis (MS) are severe neural tube defects that result in neurodevelopmental impairments and hydrocephalus due to prenatal spinal cord exposure to amniotic fluid. Fetal MMC/MS (fMMC/MS) repair has become the standard of care in appropriately selected patients, demonstrating improved outcomes, including a reduction in the need for cerebrospinal fluid (CSF) diversion compared to postnatal MMC/MS (pMMC/MS) closure. This study is a detailed analysis of the incidence, timing, and imaging predictors of hydrocephalus and CSF diversion dependence in fetal repair and postnatal closure patients in the post-MOMS trial era.

methodsA retrospective review was conducted of MMC/MS patients treated at a single institution between 2016 and 2023. Inclusion criteria required complete prenatal and postnatal follow-up data. Imaging metrics, including prenatal atrial diameter (AD) and postnatal fronto-occipital horn ratio (FOR), were analyzed alongside head circumference (HC) growth trajectories. Statistical analyses, including Youden's index, were performed to identify predictive cutoffs for shunt dependence.

resultsAmong 333 MMC/MS patients, fetal repair significantly reduced permanent CSF diversion rates compared to postnatal closure (27.8% vs. 70.1%, p < 0.01). Timing of clinical hydrocephalus onset was delayed in fetal patients (24.2 weeks vs. 2.8 weeks, p < 0.01). HC of fetal patients was highly correlated with timing of shunt dependence. AD ≥ 10 mm and postnatal FOR ≥ 0.5 were associated with higher shunt dependence (p < 0.01). Optimal cut points for predicting shunt dependence were identified by Youden's index as 14 mm for AD and 0.57 for early postnatal FOR.

conclusionFetal repair of MMC/MS decreases the incidence of clinical hydrocephalus and delays its onset compared to postnatal closure. Early imaging metrics (AD and FOR) may stratify hydrocephalus risk, enabling improved prenatal counseling and postnatal care. Long-term follow-up remains crucial for early detection and management of hydrocephalus in fetal MMC/MS patients.

Indexed as

HydrocephalusMeningomyeloceleCerebrospinal Fluid ShuntsFemaleHumansInfant, NewbornMalePregnancyRetrospective StudiesFetal repairHydrocephalusMyelomeningoceleMyeloschisisSpina bifida

Identifiers

PMID40237858
PMCPMC12003469

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