Evidence map›Paper›PMID 39030337›Full record

Observational studyChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2024

Neurosurgical management of Myelomeningocele in premature infants: a case series.

Addison Stewart, Andrew T Hale, Benjamin W Saccomano, Ariana S Barkley, Betsy D Hopson, Anastasia Arynchyna-Smith, James M Johnston, Brandon G Rocque, Jeffrey P Blount, Curtis J Rozzelle

Abstract readObservational Study
In one paragraph

Observational study in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2024. 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

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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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Addison StewartDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
Andrew T HaleDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
Benjamin W SaccomanoDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
Ariana S BarkleyDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
Betsy D HopsonDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
Anastasia Arynchyna-SmithDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
James M JohnstonDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
Brandon G RocqueDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
Jeffrey P BlountDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA.
Curtis J RozzelleDivision of Pediatric Neurosurgery, Children's of Alabama, Birmingham, AL, USA. Curtis.rozzelle@childrensal.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMyelomeningocele (MMC) is the most common neural tube defect, but rarely seen in premature infants. Most centers advocate for closure of MMC within 24 h of birth. However, this is not always possible in severely premature infants. Given the rarity of this patient population, we aimed to share our institutional experience and outcomes of severely premature infants with MMC.

methodsWe performed a retrospective, observational review of premature infants (≤ 32 weeks gestational age) identified through our multidisciplinary spina bifida clinic (1995-2021) and surgical logs. Descriptive statistics were compiled about this sample including timing of MMC closure and incidence of adverse events such as sepsis, CSF diversion, meningitis, and death.

resultsEight patients were identified (50% male) with MMC who were born ≤ 32 weeks gestational age. Mean gestational age of the population was 27.3 weeks (SD 3.5). Median time to MMC closure was 1.5 days (IQR = 1-80.8). Five patients were taken for surgery within the recommended 48 h of birth; 2 patients underwent significantly delayed closure (107 and 139 days); and one patient's defect epithelized without surgical intervention. Six of eight patients required permanent cerebrospinal fluid (CSF) diversion (2 patients were treated with ventriculoperitoneal shunting (VPS), three were treated with endoscopic third ventriculostomy (ETV) with choroid plexus cauterization (CPC) and 1 patient treated with ETV; mean of 3 years after birth, ranging from 1 day to 16 years). Two patients required more than one permanent CSF diversion procedure. Two patients developed sepsis (defined as meeting at least 2/4 SIRS criteria). In both cases of sepsis, patients developed signs and symptoms more than 72 h after birth. Notably, both instances of sepsis occurred unrelated to operative intervention as they occurred before permanent MMC closure. Two patients had intraventricular hemorrhage (both grade III). No patients developed meningitis (defined as positive CSF cultures) prior to MMC closure. Median follow up duration was 9.7 years. During this time epoch, 3 patients died: Two before 2 years of age of causes unrelated to surgical intervention. One of the two patients with grade III IVH died within 24 h of MMC closure.

conclusionsIn our institutional experience with premature infants with MMC, some patients underwent delayed MMC closure. The overall rate of meningitis, sepsis, and mortality for preterm children with MMC was similar to MMC patients born at term.

Indexed as

Infant, PrematureMeningomyeloceleNeurosurgical ProceduresFemaleHumansInfantInfant, NewbornMaleRetrospective StudiesCase seriesMyelomeningocelePrematuritySpina bifida

Identifiers

PMID39030337
PMCPMC11538150

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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.