Evidence map›Paper›PMID 41273363›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2025

Mapping the neurocognitive landscape of pediatric Chiari malformation type I: a scoping review of the literature.

Mohammed A Fouda, Asia Srhir, Elliot Zakursky, Aharnish Dev, Amanda Sacks-Zimmerman, Jeffrey P Greenfield, H Allison Bender

Abstract readScoping Review
PubMed Publisher
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
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

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

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

7 authors.

Mohammed A FoudaDepartment of Neurological Surgery, New York-Presbyterian Hospital, Weill Cornell Medicine, 525 E 68th St, New York, NY, USA. Maf4023@med.cornell.edu.ORCID 0000-0001-8884-7289
Asia SrhirDepartment of Neurological Surgery, New York-Presbyterian Hospital, Weill Cornell Medicine, 525 E 68th St, New York, NY, USA.
Elliot ZakurskyDepartment of Neurological Surgery, New York-Presbyterian Hospital, Weill Cornell Medicine, 525 E 68th St, New York, NY, USA.
Aharnish DevDepartment of Neurological Surgery, New York-Presbyterian Hospital, Weill Cornell Medicine, 525 E 68th St, New York, NY, USA.
Amanda Sacks-ZimmermanDepartment of Neurological Surgery, New York-Presbyterian Hospital, Weill Cornell Medicine, 525 E 68th St, New York, NY, USA.
Jeffrey P GreenfieldDepartment of Neurological Surgery, New York-Presbyterian Hospital, Weill Cornell Medicine, 525 E 68th St, New York, NY, USA.
H Allison BenderDepartment of Neurological Surgery, New York-Presbyterian Hospital, Weill Cornell Medicine, 525 E 68th St, New York, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to advancements in neuroimaging, Chiari malformation type I (CM-I) has become more widely recognized in pediatric populations. While its neurological manifestations are well documented, research on its neurocognitive impact remains limited and poorly characterized. This scoping review facilitates a comprehensive mapping of the current evidence, identifies the neurocognitive domains most frequently assessed, evaluates the extent of available evidence regarding surgical outcomes, and highlights critical knowledge gaps. The most frequently examined domains were working memory, executive function, language, and attention. Parental reports commonly indicated executive dysfunction, particularly within metacognitive processes. Evidence linking surgical decompression to improvements in neurocognitive function was inconsistent, and most studies lacked baseline or longitudinal assessments. Across studies, substantial methodological heterogeneity and variable use of validated instruments limited cross-comparison. Current evidence on the neurocognitive sequelae of pediatric CM-I is fragmented and methodologically diverse. The findings underscore the need for standardized neurocognitive assessments at diagnosis, the use of validated pediatric instruments, and prospective, longitudinal research integrating clinical, neuroimaging, and neurocognitive data to clarify the developmental impact of CM-I and its management.

Indexed as

Arnold-Chiari MalformationChildHumansNeuropsychological TestsChiari malformation type IExecutive functionNeurocognitivePediatricWorking memory

Identifiers

What OpenQuestion holds

Textmetadata
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.