Evidence map›Paper›PMID 27086130›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2016

Myelomeningocele - a single institute analysis of the years 2007 to 2015.

Elke Januschek, Andreas Röhrig, Sandra Kunze, Christian Fremerey, Bea Wiebe, Martina Messing-Jünger

Abstract read
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In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
28.7field-weighted citation impact, top 1% of its field
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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 122 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Differences in brain development and need for CSF diversion based on MMC level: Comparison between prenatal and postnatal repair.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Myelomeningocele as an anomaly of secondary neurulation.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022
    Article
  11. Article
  12. Retrospective analysis of early- and late-operated meningomyelocele patients.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Article
  13. Shunt timing in meningomyelocele and clinical results: analysis of 80 cases.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Article
  14. Shunt revision rates in myelomeningocele patients in the first year of life: a retrospective study of 52 patients.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2018
    Article
  15. How much do plastic surgeons add to the closure of myelomeningoceles?Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2018
    Article
  16. The problem with myelomeningoceles, hydrocephalus, and progressive neurological deficits-what do we know?Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2017
    Article
  17. Article
  18. A comparison of the MOMS trial results to a contemporaneous, single-institution, postnatal closure cohort.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Elke JanuschekNeurosurgical Department, Sana Klinikum Offenbach GmbH, Starkenburgring 66, 63069, Offenbach, Germany. e.januschek@gmx.de.
Andreas RöhrigNeurosurgical Department, Asklepios Children's Hospital, Arnold-Janssen Straße 29, 53757, Sankt Augustin, Germany.
Sandra KunzeNeurosurgical Department, Asklepios Children's Hospital, Arnold-Janssen Straße 29, 53757, Sankt Augustin, Germany.
Christian FremereyDepartment of Neonatology and Pediatric Intensive Care Medicine, Asklepios Children's Hospital, Arnold-Janssen Straße 29, 53757, Sankt Augustin, Germany.
Bea WiebeDepartment of Neonatology and Pediatric Intensive Care Medicine, Asklepios Children's Hospital, Arnold-Janssen Straße 29, 53757, Sankt Augustin, Germany.
Martina Messing-JüngerNeurosurgical Department, Asklepios Children's Hospital, Arnold-Janssen Straße 29, 53757, Sankt Augustin, Germany.
Asklepios Klinik Sankt Augustin · DESana Klinikum Offenbach · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAfter the introduction of folate supplementation, the number of open spinal dysraphism was successfully reduced over time. In 2007, the department for pediatric neurosurgery was established in the children's hospital. Since then, newborns with myelomeningocele (MMC), the most common form of open neural tube defects (NTD), are treated here. The aim of this study is to present the concepts applied to and experiences resulting from treatment of MMC.

methodsRecords of all newborns with MMC treated surgically during the period January 2007 to August 2015 in our institution were analyzed. Children, who were previously operated in utero were excluded. The type of neural tube defect, its location, associated comorbidities, and ambulation were recorded.

resultsForty-eight children (25 males, 23 females) with spinal dysraphism were included in the analysis. In nearly 90 % of the cases, the repair of the MMC was done on the day of delivery. The follow-up period ranges from 9 weeks to 8 9/12 years (loss of follow-up in 2 cases). In 19 %, the defect remained undetected during gestation and in one case, carbamazepine was taken despite pregnancy. In 36 children (75 %), we found a Chiari malformation type II (CMII) associated with myelomeningocele. 85.4 % suffered from hydrocephalus and implantation of a shunt was necessary. In cases of bladder impairment, an intermittent catheterization was the most common management (83.3 %); no bladder augmentation was required. Twelve children required orthopedic surgery. Twenty-three of 33 patients (70 %) are ambulatory w/wo orthoses and devices. The 13 children who are younger than 2 years were considered separately to assess the motor activity safely.

conclusionsOur data show that neural tube defects to this day can remain undetected despite medical care during pregnancy. The most common associated diseases with MMC are Chiari II malformations and hydrocephalus. In the seven cases of simultaneous repair of MMC with shunt implantation, no additional complications were encountered. An interdisciplinary approach was allowed in a high percentage independence and social continence.

Indexed as

MeningomyeloceleChildChild, PreschoolFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleRetrospective StudiesChiari malformationHydrocephalusNeural tube defectSpinal dysraphism

Identifiers

PMID27086130
OpenAlexW2339565574

What OpenQuestion holds

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Read underepoch 390

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.