Evidence map›Paper›PMID 34232379›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2021

Long-term outcomes of posterior fossa decompression for Chiari malformation type 1: which patients are most prone to failure?

Khashayar Mozaffari, Laurence Davidson, Eric Chalif, Tiffany N Phan, Andrew D Sparks, John S Myseros, Chima O Oluigbo, Robert F Keating

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Chiari type 1 malformations and hypermobility spectrum disorder: clinical outcomes and the importance of the differential diagnosis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  4. Article
  5. Article
  6. Complication Avoidance in Chiari Malformation Surgery.Advances and technical standards in neurosurgery · 2024
    Review
  7. Review
  8. Article
  9. Article
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

8 authors at 3 institutions in 1 country.

Khashayar MozaffariGeorge Washington University School of Medicine and Health Sciences, Washington, DC, USA. kmozaffari@gwmail.gwu.edu.ORCID http://orcid.org/0000-0002-6848-4211
Laurence DavidsonDivision of Neurosurgery, Children's National Hospital, Washington, DC, USA.
Eric ChalifGeorge Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Tiffany N PhanDivision of Neurosurgery, Children's National Hospital, Washington, DC, USA.
Andrew D SparksDepartment of Surgery, The George Washington University Hospital, Washington, DC, USA.
John S MyserosDivision of Neurosurgery, Children's National Hospital, Washington, DC, USA.
Chima O OluigboDivision of Neurosurgery, Children's National Hospital, Washington, DC, USA.
Robert F KeatingDivision of Neurosurgery, Children's National Hospital, Washington, DC, USA.
Children's National · USGeorge Washington University · USGeorge Washington University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe role of an osseous-only posterior fossa decompression (PFD) for Chiari malformation type 1 (CM1) remains controversial. We reviewed long-term outcomes for patients with CM1 undergoing a PFD to evaluate if there was any difference for failure when compared to patients undergoing a PFD with duraplasty (PFDD).

methodsConsecutive patients surgically treated at a single tertiary pediatric neurosurgery clinic over a 25-year period with at least 5 years of follow-up were evaluated. PFD patients were compared to those that initially received a PFDD. Demographics, surgical indications, surgical approach, outcomes, and complications were reviewed.

resultsA total of 60 patients were included in this study of which 25 (41.67%) underwent PFD and 35 (58.33%) underwent PFDD. Mean age at surgery was 7.41 years (range 0.4 to 18 years) with a mean follow-up of 8.23 years (range 5 to 21 years). Those that received a PFD had a lower rate of radiographic syrinx improvement (p = 0.03), especially in the setting of holocord syringes. Failure rate was significantly higher in the PFD group (20% vs 2.90%, p = 0.03). However, complications were significantly higher in the PFDD group (17.14% vs 4.0%, p = 0.04).

conclusionsPFD provides a safe treatment option with similar clinical improvements and lower post-operative complication rate compared to PFDD, albeit at the cost of greater chance of reoperation, especially in the setting of a holocord syrinx. Patients with a holocord syrinx should be considered for a PFDD as their initial procedure.

Indexed as

Arnold-Chiari MalformationSyringomyeliaAdolescentChildChild, PreschoolDecompression, SurgicalDura MaterHumansInfantRetrospective StudiesTreatment OutcomeYoung AdultChiari malformationDuraplastyLong-termSyringomyeliaSyrinx

Identifiers

PMID34232379
OpenAlexW3181154716

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.