Evidence map›Paper›PMID 42159779›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2026

Pediatric complex Chiari I Malformation-how complex is it?

Amparo Saenz, Honglin Zhu, Jasneet Dhaliwal, Sniya Sudhakar, Kshitij Mankad, Dominic Thompson, M Zubair Tahir

Abstract read
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2026. 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Amparo SaenzPediatric Neurosurgery Department, Great Ormond Street Hospital, London, UK. amparo.saenz@ucl.ac.uk.
Honglin ZhuPediatric Neurosurgery Department, Great Ormond Street Hospital, London, UK.
Jasneet DhaliwalPediatric Neurosurgery Department, Great Ormond Street Hospital, London, UK.
Sniya SudhakarPediatric Neuroradiology Department, Great Ormond Street Hospital, London, UK.
Kshitij MankadPediatric Neuroradiology Department, Great Ormond Street Hospital, London, UK.
Dominic ThompsonPediatric Neurosurgery Department, Great Ormond Street Hospital, London, UK.
M Zubair TahirPediatric Neurosurgery Department, Great Ormond Street Hospital, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPediatric complex Chiari I Malformation (CCM), defined by Chiari I with additional craniovertebral junction anomalies, has been associated with higher failure rates following foramen magnum decompression (FMD) alone, leading some to advocate occipitocervical fixation (OCF) or ventral decompression. This study evaluates a single-institution experience with isolated FMD in CCM.

methodsPatients meeting CCM criteria were identified from a prospective surgical database from March 2020 to December 2023. Patients with incomplete imaging or < 6-month follow-up were excluded. Pre- and postoperative imaging assessed tonsillar descent, brainstem crowding, CSF flow, and syringomyelia. Clinical outcome was recorded.

resultsSixty patients met the inclusion criteria for CCM, but nineteen patients were excluded. Forty-one CCM patients underwent FMD. Headache prevalence decreased from 73.2% preoperatively to 7.3% at last follow-up (p < 0.001). One patient (2.4%) required reoperation for inadequate decompression. Median tonsillar descent improved from 15.0 to 0.0 mm (p < 0.001), and obex ectopia from 7.0 to 0.0 mm (p < 0.001). Anterior and posterior CSF effacement significantly improved. Craniocervical angle increased from 122.0 to 130.0° (p = 0.007), and pb-C2 distance decreased from 7.0 to 5.0 mm (p < 0.001). No patient required OCF or ventral decompression during a mean 2.1-year follow-up.

conclusionIsolated FMD provides effective clinical and radiological improvement in most pediatric CCM patients. Routine addition of OCF or ventral decompression may be unnecessary, preserving cervical mobility while minimizing morbidity.

Indexed as

Arnold-Chiari MalformationDecompression, SurgicalForamen MagnumAdolescentChildChild, PreschoolFemaleHumansMaleTreatment OutcomeChiari malformationForamen magnum decompressionPediatric neurosurgerySpine

Identifiers

PMID42159779
PMCPMC13190738

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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.