Evidence map›Paper›PMID 41639295›Full record

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

Preoperative hydrocephalus and the risk of postoperative speech impairment following posterior fossa tumour surgery in children: results from a prospective, multinational cohort study.

Aske Foldbjerg Laustsen, Radek Frič, Jonathan Kjær Grønbæk, Vladimír Beneš, Vicente Santa-Maria Lopez, Ulf Nestler, Andrea Carai, Guirish Solanki, Shivaram Avula, Conor Malluci and 17 more

Registry-linked trialAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study 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. It is linked to trial NCT02300766 (Nordic Study of the Cerebellar Mutism Syndrome in Children With Brain Tumours of the Posterior Fossa), which is not on this 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.

NCT02300766 recruitingnot on this map

Nordic Study of the Cerebellar Mutism Syndrome in Children With Brain Tumours of the Posterior Fossa

Typeobservational_patient_registrySponsorRigshospitalet, DenmarkRan2014 to 2028Enrolled2,000ConditionsInfratentorial Neoplasms, Mutism
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

27 authors.

Aske Foldbjerg LaustsenDepartment of Neurosurgery, Rigshospitalet, Copenhagen, Denmark. aske.foldbjerg.laustsen@regionh.dk.
Radek FričDepartment of Neurosurgery, University Hospital Oslo-Rikshospitalet, Oslo, Norway.
Jonathan Kjær GrønbækDepartment of Neurosurgery, Rigshospitalet, Copenhagen, Denmark.
Vladimír BenešDepartment of Neurosurgery, 2nd Medical Faculty and Motol University Hospital, Prague, Czechia.
Vicente Santa-Maria LopezNeuro-Oncology Unit, Pediatric Cancer Center Barcelona, Hospital Sant Joan de Déu, Barcelona, Spain.
Ulf NestlerDepartment of Neurosurgery, Fondation Lenval Children's Hospital, Nice, France.
Andrea CaraiDepartment of Neurosurgery, Bambino Gesù Children's Hospital, Rome, Italy.
Guirish SolankiDepartment of Paediatric Neurosurgery, Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
Shivaram AvulaDepartment of Radiology, Alder Hey Children's NHS Foundation, Liverpool, UK.
Conor MalluciDepartment of Neurosurgery, Alder Hey Children's NHS Trust, Liverpool, UK.
Pelle NilssonDepartment of Medical Sciences/Neurosurgery, Uppsala University, Uppsala University Hospital, Uppsala, Sweden.
Per NymanCrown Princess Victoria Children's Hospital, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Magnus Aasved HjortDepartment of Pediatric Hematology and Oncology, St. Olavs Hospital, Trondheim, Norway.
Rick BrandsmaPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.
Eelco HovingPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.
Antonella BuaDepartment of Neurosurgery, Bambino Gesù Children's Hospital, Rome, Italy.
Jana TáborskáDepartment of Neurosurgery, 2nd Medical Faculty and Motol University Hospital, Prague, Czechia.
Katalin Mudra2nd, Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Markia Balázs2nd, Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Giedre RutkaiskieneDepartment of Pediatrics, Lithuanian University of Health Science, Kaunas, Lithuania.
Saulius RočkaClinic of Neurology and Neurosurgery, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
Jurgen LemierePediatric Oncology, Department of Oncology, KU Leuven, Louvain, Belgium.
Florian WilhelmyDepartment of Neurosurgery, University Hospital Leipzig, Leipzig, Germany.
Christian DorferDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Astrid SehestedDepartment of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark.
Marianne Juhler *Department of Neurosurgery, Rigshospitalet, Copenhagen, Denmark.
René Mathiasen *Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCerebellar mutism syndrome (CMS) is a common complication of paediatric posterior fossa (PF) tumour surgery, with postoperative speech impairment (POSI) as the cardinal symptom. Preoperative hydrocephalus (pHC) is present in up to 70% of cases of paediatric PF tumours, but its association with POSI remains unclear. This study investigated whether pHC is an independent risk factor for POSI and assessed the impact of alleviating pHC prior to tumour resection on POSI risk.

methodsWe included 800 children who underwent PF tumour surgery between 2014 and 2024 at 35 centres across 13 countries in the European CMS study. Speech and neurological assessments were conducted pre- and postoperatively. Neurosurgeons assessed pHC status, pHC treatment and tumour location; histology was recorded at a 2-month follow-up. pHC treatment was categorised as "yes" (pHC alleviated prior to tumour surgery) and "no" (pHC alleviated by tumour surgery alone). POSI was categorised as "habitual speech", "reduced speech" or "mutism".

resultsOf 800 patients, 515 (64%) had pHC. Absence of pHC was associated with lower POSI risk in univariate analysis (OR 0.51 (95% CI 0.35; 0.76)), but this reversed and became non-significant after adjustment (1.20 (0.60; 2.41)). pHC treatment was associated with an increased POSI risk in the univariate analysis (1.93 (1.14; 3.26)), which became non-significant in the adjusted analysis (1.15 (0.60; 2.21)).

conclusionThe presence of pHC was not independently associated with POSI nor did treatment of pHC prior to tumour resection appear to reduce the risk of POSI. These findings highlight the importance of individualizing pHC management in paediatric PF tumour cases, with decisions guided by the clinical context.

trial registrationClinical Trials ID NCT02300766 (October 2014).

Indexed as

HydrocephalusInfratentorial NeoplasmsNeurosurgical ProceduresPostoperative ComplicationsSpeech DisordersAdolescentChildChild, PreschoolCohort StudiesFemaleHumansInfantMaleMutismProspective StudiesRisk FactorsCerebellar mutism syndromePaediatric posterior fossa tumourPosterior fossa syndromePreoperative hydrocephalus

Identifiers

PMID41639295
PMCPMC12872776

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.