Evidence map›Paper›PMID 39015767›Full record

ArticleBrain communications2024

Neuroanatomy of cerebellar mutism syndrome: the role of lesion location.

Jax Skye, Joel Bruss, Sebastian Toescu, Kristian Aquilina, Amanda Grafft, Gino Bardi Lola, Aaron D Boes

Abstract read
In one paragraph

Article in Brain communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Jax SkyeDepartment of Neurology, University of Iowa Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.ORCID https://orcid.org/0000-0001-7873-1469
Joel BrussDepartment of Neurology, University of Iowa Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Sebastian ToescuDepartment of Neurosurgery, Great Ormond Street Hospital, London WC1N 3JH, UK.ORCID https://orcid.org/0000-0001-8768-9231
Kristian AquilinaDepartment of Neurosurgery, Great Ormond Street Hospital, London WC1N 3JH, UK.ORCID https://orcid.org/0000-0001-7015-5196
Amanda GrafftDepartment of Pediatrics, Division of Developmental and Behavioral Pediatrics, University of Iowa Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Gino Bardi LolaDepartment of Pediatrics, Division of Hematology/Oncology, University of Iowa Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Aaron D BoesDepartment of Neurology, University of Iowa Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.ORCID https://orcid.org/0000-0002-7865-9257

Funding

Predicting Cognitive Outcomes from Stroke Based on Lesion LocationR01NS114405 · NINDS · UNIVERSITY OF IOWA · PI BOES, AARON D · 2020 to 2024
$2.1M
NINDS NIH HHS R01 NS114405
6 · The paper itself

Abstract

Approximately 25% of paediatric patients who undergo cerebellar tumour resection develop cerebellar mutism syndrome. Our group recently showed that damage to the cerebellar deep nuclei and superior cerebellar peduncles, which we refer to as the cerebellar outflow pathway, is associated with an increased risk of cerebellar mutism syndrome. Here, we tested whether these findings replicate in an independent cohort. We evaluated the relationship between lesion location and the development of cerebellar mutism syndrome in an observational study of 56 paediatric patients ranging from five months to 14 years of age who underwent cerebellar tumour resection. We hypothesized that individuals who developed cerebellar mutism syndrome after surgery, relative to those who did not, would have lesions that preferentially intersect with: (i) the cerebellar outflow pathway and (ii) a previously generated 'lesion-symptom map' of cerebellar mutism syndrome. Analyses were conducted in accordance with pre-registered hypotheses and analytic methods (https://osf.io/r8yjv/). We found supporting evidence for both hypotheses. Compared to patients who did not develop cerebellar mutism syndrome, patients with cerebellar mutism syndrome (

Indexed as

brainstem tumourcerebellar cognitive affective syndromecerebellar mutism syndromecerebellum diseaseposterior fossa tumour

Identifiers

PMID39015767
PMCPMC11250198

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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.