Evidence map›Paper›PMID 39652857›Full record

ArticleJournal of neurosurgery. Case lessons2024

Spinal cord-spinal canal disproportion following treatment for syringomyelia associated with Chiari malformation type I: illustrative case.

Arjun Nair, Vivek P Gupta, Devin Kolmetzky, Jennifer M Strahle, David D Limbrick

Abstract read
In one paragraph

Article in Journal of neurosurgery. Case lessons, 2024. 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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0citing papers in PubMed
–field-weighted citation impact
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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Arjun NairDepartment of Neurological Surgery, Washington University in Saint Louis School of Medicine, Saint Louis, Missouri.
Vivek P GuptaDepartment of Neurological Surgery, Washington University in Saint Louis School of Medicine, Saint Louis, Missouri.
Devin KolmetzkyPhiladelphia College of Osteopathic Medicine, Philadelphia, Pennsylvania.
Jennifer M StrahleDepartment of Neurological Surgery, Washington University in Saint Louis School of Medicine, Saint Louis, Missouri.
David D LimbrickDepartment of Neurological Surgery, Virginia Commonwealth University, Richmond, Virginia.

Funding

Redefining Chiari Type I Malformation through Genetically, Radiologically, and Clinically-Derived Endophenotypes that are Predictive of Long-Term Neurological OutcomeP01NS131131 · NINDS · WASHINGTON UNIVERSITY · PI David Delmar Limbrick, Chenyang Lu · 2023 to 2026
$7.6M
NINDS NIH HHS P01 NS131131
6 · The paper itself

Abstract

backgroundChiari malformation type I (CM-I) is a common pediatric neurosurgical condition that is often associated with syringomyelia (SM) and spine deformity. The association of these three conditions is well recognized, but the pathophysiology linking them has yet to be fully elucidated. OBSERVATIONS: This case report describes the unusual course of a 13-year-old male with CM-I, a large holocord syrinx, and progressive scoliosis who developed an angiography-negative subarachnoid hemorrhage (SAH) 4 months after successful posterior fossa decompression with duraplasty (PFDD). Notably, his cervical spinal canal diameter was increased relative to normative data. After presenting with SAH, he was treated with a course of lumbar cerebrospinal fluid drainage, which relieved his symptoms, and he had no further incidents. His syrinx responded to PFDD with a dramatic decrease in spinal cord diameter, in contradistinction to his dilated bony spinal canal. He is presently 4 years out from his SAH and doing well clinically. LESSONS: This report describes the first case of nonaneurysmal SAH following PFDD for CM-I and SM and explores a possible link between SM and bony spinal canal diameter. https://thejns.org/doi/10.3171/CASE24272.

Indexed as

Chiari malformation type Ispinal canal dilationsyringomyelia

Identifiers

PMID39652857
PMCPMC11633020

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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.