Evidence map›Paper›PMID 30141752›Full record

ArticleJournal of neurosurgery. Pediatrics2018

Decompression for Chiari malformation type II in individuals with myelomeningocele in the National Spina Bifida Patient Registry.

Irene Kim, Betsy Hopson, Inmaculada Aban, Elias B Rizk, Mark S Dias, Robin Bowman, Laurie L Ackerman, Michael D Partington, Heidi Castillo, Jonathan Castillo and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neurosurgery. Pediatrics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Surgical management of Chiari II malformation: a systematic review of literature.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Sleep-related breathing disorders in children with spina bifida.Journal of pediatric rehabilitation medicine · 2024
    Review
  6. Article
  7. Myelomeningocele: Long-Term Neurosurgical Management.Advances and technical standards in neurosurgery · 2024
    Review
  8. Article
  9. Current status and challenges of neurosurgical procedures for patients with myelomeningocele in real-world Japan.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2023
    Article
  10. Myelomeningocele: the evolution of care over the last 50 years.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2023
    Review
  11. 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
  12. Fetal Surgery for Myelomeningocele: Neurosurgical Perspectives.Advances and technical standards in neurosurgery · 2023
    Article
  13. Multidisciplinary spina bifida clinic: the Chicago experience.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022
    Review
  14. Pediatric Spina Bifida and Spinal Cord Injury.Journal of personalized medicine · 2022
    Article
  15. Determination of anatomic level of myelomeningocele by prenatal ultrasound.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022
    Article
  16. Article
  17. Observational
  18. Surgical management of Chiari malformation type II.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 7 institutions in 1 country.

Irene Kim1Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, Wisconsin.
Betsy Hopson2Department of Neurosurgery, University of Alabama at Birmingham, Children's of Alabama, Birmingham.
Inmaculada Aban3Department of Biostatistics, University of Alabama at Birmingham, Alabama.
Elias B Rizk4Department of Neurological Surgery, Penn State College of Medicine, Hershey, Pennsylvania.
Mark S Dias4Department of Neurological Surgery, Penn State College of Medicine, Hershey, Pennsylvania.
Robin Bowman5Pediatric Neurosurgery, Lurie Children's Hospital of Chicago, Illinois.
Laurie L Ackerman6Goodman Campbell Brain and Spine Division of Pediatric Neurosurgery, Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Michael D Partington7Department of Neurosurgery, University of Kansas, Kansas City, Kansas.
Heidi Castillo8Department of Pediatrics, Baylor College of Medicine, Houston, Texas; and.
Jonathan Castillo8Department of Pediatrics, Baylor College of Medicine, Houston, Texas; and.
Paula R Peterson9Department of Neurology, University of Utah, Salt Lake City, Utah.
Jeffrey P Blount2Department of Neurosurgery, University of Alabama at Birmingham, Children's of Alabama, Birmingham.
Brandon G Rocque2Department of Neurosurgery, University of Alabama at Birmingham, Children's of Alabama, Birmingham.
University of Alabama at Birmingham · USNeurological Surgery · USBaylor College of Medicine · USChildren's of Alabama · USLurie Children's Hospital · USMedical College of Wisconsin · USUniversity of Kansas · 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
Comp B-Texas Children's Hospital and Baylor Coll of Med Spina Bifida RegistryU01DD001072 · DD · BAYLOR COLLEGE OF MEDICINE · PI CASTILLO, HEIDI, KOH, CHESTER · 2014 to 2018
$327k
Comp B-National Spina Bifida Registry-Lurie Children's HospitalU01DD001091 · DD · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI BOWMAN, ROBIN, CHENG, EARL Y · 2014 to 2018
$327k
NCBDD CDC HHS U01 DD000742NCBDD CDC HHS U01 DD000766NCBDD CDC HHS U01 DD000772NCBDD CDC HHS U01 DD001072NCBDD CDC HHS U01 DD001091NCBDD CDC HHS U01 DD001265
6 · The paper itself

Abstract

OBJECTIVEThe purpose of this study was to determine the rate of decompression for Chiari malformation type II in individuals with myelomeningocele in the National Spina Bifida Patient Registry (NSBPR). In addition, the authors explored the variation in rates of Chiari II decompression across NSBPR institutions, examined the relationship between Chiari II decompression and functional lesion level of the myelomeningocele, age, and need for tracheostomy, and they evaluated for temporal trends in rates of Chiari II decompression.METHODSThe authors queried the NSBPR to identify all individuals with myelomeningocele between 2009 and 2015. Among these patients, they identified individuals who had undergone at least 1 Chiari II decompression as well as those who had undergone tracheostomy. For each participating NSBPR institution, the authors calculated the proportion of patients enrolled at that site who underwent Chiari II decompression. Logistic regression was performed to analyze the relationship between Chiari II decompression, functional lesion level, age at decompression, and history of tracheostomy.RESULTSOf 4448 individuals with myelomeningocele identified from 26 institutions, 407 (9.15%) had undergone at least 1 Chiari II decompression. Fifty-one patients had undergone tracheostomy. Logistic regression demonstrated a statistically significant relationship between Chiari II decompression and functional lesion level of the myelomeningocele, with a more rostral lesion level associated with a higher likelihood of posterior fossa decompression. Similarly, children born before 2005 and those with history of tracheostomy had a significantly higher likelihood of Chiari II decompression. There was no association between functional lesion level and need for tracheostomy. However, among those children who underwent Chiari II decompression, the likelihood of also undergoing tracheostomy increased significantly with younger age at decompression.CONCLUSIONSThe rate of Chiari II decompression in patients with myelomeningocele in the NSBPR is consistent with that in previously published literature. There is a significant relationship between Chiari II decompression and functional lesion level of the myelomeningocele, which has not previously been reported. Younger children who undergo Chiari II decompression are more likely to have undergone tracheostomy. There appears to be a shift away from Chiari II decompression, as children born before 2005 were more likely to undergo Chiari II decompression than those born in 2005 or later.

Indexed as

AdolescentAdultAgedAged, 80 and overArnold-Chiari MalformationChildChild, PreschoolDecompression, SurgicalFemaleFollow-Up StudiesHumansInfantInfant, NewbornMaleMeningomyeloceleMiddle AgedCDC = Centers for Disease Control and PreventionChiari II malformationmyelomeningoceleNSBPR = National Spina Bifida Patient Registryposterior fossa decompressionspina bifidatracheostomy

Identifiers

PMID30141752
PMCPMC8934589
OpenAlexW2888726419

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.