Evidence map›Paper›PMID 33386749›Full record

ArticleDevelopmental medicine and child neurology2021

Neurosurgical procedures for children with myelomeningocele after fetal or postnatal surgery: a comparative effectiveness study.

Gordon Worley, Rachel G Greenberg, Brandon G Rocque, Tiebin Liu, Brad E Dicianno, Jonathan P Castillo, Elisabeth A Ward, Tonya R Williams, Jeffrey P Blount, John S Wiener

Open access · greenAbstract read
In one paragraph

Article in Developmental medicine and child neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Outcomes in prenatal vs. postnatal surgery for myelomeningocele: a systematic review and meta-analysis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2025
    Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Regression of Chiari malformation type 2 following early postnatal meningomyelocele repair-a retrospective observation from an institutional series of patients.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Article
  6. Article
  7. Article
  8. What has changed in pediatric neurosurgical care in spina bifida? A 30-year UAB/Children's of Alabama observational overview.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2023
    Article
  9. Article
  10. Fetal Surgery for Myelomeningocele: Neurosurgical Perspectives.Advances and technical standards in neurosurgery · 2023
    Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 1 country.

Gordon WorleyDivision of Pediatric Neurology and Developmental Medicine, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0001-5127-2514
Rachel G GreenbergDivision of Neonatology, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
Brandon G RocqueDivision of Pediatric Neurosurgery, Department of Neurosurgery, Children's Hospital of Alabama, University of Alabama at Birmingham, Birmingham, AL, USA.
Tiebin LiuDivision of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Brad E DiciannoDepartment of Physical Medicine and Rehabilitation, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Jonathan P CastilloDivision of Developmental Pediatrics, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Elisabeth A WardDivision of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Tonya R WilliamsDivision of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Jeffrey P BlountDivision of Pediatric Neurosurgery, Department of Neurosurgery, Children's Hospital of Alabama, University of Alabama at Birmingham, Birmingham, AL, USA.
John S WienerDivision of Urology, Department of Surgery, Duke University Medical Center, Durham, NC, USA.
Centers for Disease Control and Prevention · USChildren's of Alabama · USDuke Medical Center · USBaylor College of Medicine · USDuke University · USUniversity of Pittsburgh · US

Funding

Research Approaches to Improve the Care and Outcomes of People Living with Spina BifidaU01DD001265 · DD · BAYLOR COLLEGE OF MEDICINE · PI CASTILLO, HEIDI, TU, DUONG DAI · 2019 to 2023
$456k
National Spina Bifida Patient Registry and Urologic Management of Young Children with Spina Bifida - Component BU01DD001278 · DD · DUKE UNIVERSITY · PI ROUTH, JONATHAN C, WIENER, JOHN SAMUEL · 2019 to 2023
$456k
Comp B-Natl SB Patient Registry and Urologic Management of Young Children with SB- Duke ProjectU01DD001082 · DD · DUKE UNIVERSITY · PI WIENER, JOHN SAMUEL · 2014 to 2018
$326k
Urologic Management to Preserve Initial Renal Function Protocol for Young Children with Spina Bifida (UMPIRE) at Texas Children's Hospital/Baylor College of MedicineU01DD001263 · DD · BAYLOR COLLEGE OF MEDICINE · PI JAROSZ, SUSAN · 2019 to 2023
$141k
NCBDD CDC HHS U01 DD001082NCBDD CDC HHS U01 DD001263NCBDD CDC HHS U01 DD001265NCBDD CDC HHS U01 DD001278
6 · The paper itself

Abstract

aimTo compare the frequencies of neurosurgical procedures to treat comorbid conditions of myelomeningocele in patients who underwent fetal surgery versus postnatal surgery for closure of the placode.

methodBy utilizing the National Spina Bifida Patient Registry in a comparative effectiveness study, 298 fetal surgery patients were matched by birthdate (±3mo) and spina bifida clinic site with one to three postnatal surgery patients (n=648). Histories were obtained by record review on enrollment and yearly subsequently. Multivariable Poisson regression was used to compare frequencies of procedures between cohorts, with adjustments for sex, ethnicity, insurance status, spinal segmental level of motor function, age at last visit recorded in the Registry, and, for shunt revision in shunted patients, age at cerebrospinal fluid (CSF) diversion.

resultsThe median age at last visit was 4 years. In fully adjusted analyses in patients aged at least 12 months old, fetal surgery was associated with decreased frequency of CSF diversion for hydrocephalus by ventriculoperitoneal shunt insertion or endoscopic third ventriculostomy compared with postnatal surgery (46% vs 79%; incidence rate ratio=0.61; 95% confidence interval [CI] 0.53-0.71; p<0.01). Over all ages, fetal surgery was associated with decreased frequency of Chiari decompression for brainstem dysfunction (3% vs 7%; incidence rate ratio=0.41; 95% CI 0.19-0.88; p=0.02). Also over all ages, differences were not significant in frequencies of shunt revision in shunted patients (53% vs 55%; incidence rate ratio=0.87; 95% CI 0.69-1.11; p=0.27), nor tethered cord release for acquired spinal cord dysfunction (18% vs 16%; incidence rate ratio=1.11; 95% CI 0.84-1.47; p=0.46).

interpretationEven with the variations inherent in clinical practice, fetal surgery was associated with lower frequencies of CSF diversion and of Chiari decompression, independent of covariates. What this paper adds Fetal surgery was associated with lower frequencies of cerebrospinal fluid diversion and decompression of Chiari II malformation than postnatal surgery. Frequencies of ventriculoperitoneal shunt revision and tethered cord release were not significantly different between cohorts.

Indexed as

Ventriculoperitoneal ShuntChildChild, PreschoolFemaleHumansHydrocephalusInfantMaleMeningomyeloceleNeurosurgical ProceduresSpinal DysraphismTreatment Outcome

Identifiers

PMID33386749
PMCPMC8603138
OpenAlexW3114800945

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.