Evidence map›Paper›PMID 35157109›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2022

Postoperative speech impairment and cranial nerve deficits after secondary surgery of posterior fossa tumours in childhood: a prospective European multicentre study.

J Kjær Grønbæk, S Toescu, R Frič, P Nilsson, C Castor, C Mallucci, B Pizer, K Aquilina, E Molinari, M Aasved Hjort and 14 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Proceedings of the first global meeting of the Posterior Fossa Society: state of the art in cerebellar mutism syndrome.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Article
  5. Article
  6. The Cerebellar Mutism Syndrome: Risk Assessment, Prevention and Treatment.Advances and technical standards in neurosurgery · 2023
    Article
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

24 authors at 14 institutions in 9 countries.

J Kjær GrønbækDepartment of Neurosurgery, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen E, Denmark. jonathan.kjaer.groenbaek@regionh.dk.ORCID 0000-0002-7170-422X
S ToescuDepartment of Neurosurgery, Great Ormond Street Hospital for Children, Great Ormond Street, London, WC1N 3JH, UK.
R FričDepartment of Neurosurgery, Oslo University Hospital, Postboks 4950 Nydalen, 0424, Oslo, Norway.
P NilssonDepartment of Neuroscience, Section of Neurosurgery, Uppsala University Hospital, 751 85, Uppsala, Sweden.
C CastorDepartment of Health Sciences, Lund University, Box 117, 221 00, Lund, Sweden.
C MallucciDepartment of Paediatric Neurosurgery, Alder Hey Children's NHS Foundation Trust, E. Prescot Road, Liverpool, L14 5AB, UK.
B PizerSchool of Health and Life Sciences, University of Liverpool, Brownlow Hill, Liverpool, L69 3BX, UK.
K AquilinaDepartment of Neurosurgery, Great Ormond Street Hospital for Children, Great Ormond Street, London, WC1N 3JH, UK.
E MolinariDepartment of Neurology, The Queen Elizabeth University Hospital, University of Glasgow, University Avenue, Glasgow, G12 8QQ, UK.
M Aasved HjortDepartment of Pediatric Hematology and Oncology, St Olavs Hospital, Postboks 3250 Torgarden, 7006, Trondheim, Norway.
A KarppinenDepartment of Neurosurgery, Helsinki University Hospital and University of Helsinki, P.O. Box 266, N00029, Helsinki, Finland.
G RutkauskieneDepartment of Pediatrics, Lithuanian University of Health Science, Mickeviciaus 9, 44307, Kaunas, Lithuania.
K Mudra2Nd Department of Pediatrics, Semmelweis University, Tűzoltó street 7-9, Budapest, Hungary.
B MarkiaNeurology and Neurosurgery, National Institute of Mental Health, Laky Adolf u. 44, 1145, Budapest, Hungary.
K van BaarsenPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584 CS, Utrecht, The Netherlands.
E HovingPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584 CS, Utrecht, The Netherlands.
J ZipfelDepartment of Neurosurgery, Pediatric Neurosurgery, University Hospital Tuebingen, Hoppe-Seyler-Str. 3, 72076, Tuebingen, Germany.
M WibroeDepartment of Paediatrics and Adolescent Medicine, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen E, Denmark.
K NysomDepartment of Paediatrics and Adolescent Medicine, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen E, Denmark.
K SchmiegelowDepartment of Paediatrics and Adolescent Medicine, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen E, Denmark.
A SehestedDepartment of Paediatrics and Adolescent Medicine, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen E, Denmark.
R MathiasenDepartment of Paediatrics and Adolescent Medicine, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen E, Denmark.
M JuhlerDepartment of Neurosurgery, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen E, Denmark.
CMS study group
Copenhagen University Hospital · DKGreat Ormond Street Hospital · GBPrincess Máxima Center · NLUniversity of Copenhagen · DKAlder Hey Children's NHS Foundation Trust · GBLithuanian University of Health Sciences · LTLund University · SEOslo University Hospital · NOQueen Elizabeth University Hospital · GBSemmelweis University · HUSt Olav's University Hospital · NOUniversity of Helsinki · FIUniversity of Liverpool · GBUppsala University Hospital · SE

Funding

Barncancerfonden PR2012-0106, KP2019-0014Børnecancerfonden 2012-9, 2014-3, 2015-14, 2016-0143, 2018-3653, 2020-6732
6 · The paper itself

Abstract

purposeBrain tumours constitute 25% of childhood neoplasms, and half of them are in the posterior fossa. Surgery is a fundamental component of therapy, because gross total resection is associated with a higher progression-free survival. Patients with residual tumour, progression of residual tumour or disease recurrence commonly require secondary surgery. We prospectively investigated the risk of postoperative speech impairment (POSI) and cranial nerve dysfunction (CND) following primary and secondary resection for posterior cranial fossa tumours.

methodsIn the Nordic-European study of the cerebellar mutism syndrome, we prospectively included children undergoing posterior fossa tumour resection or open biopsy in one of the 26 participating European centres. Neurological status was assessed preoperatively, and surgical details were noted post-operatively. Patients were followed up 2 weeks, 2 months and 1 year postoperatively. Here, we analyse the risk of postoperative speech impairment (POSI), defined as either mutism or reduced speech, and cranial nerve dysfunction (CND) following secondary, as compared to primary, surgery.

resultsWe analysed 426 children undergoing primary and 78 undergoing secondary surgery between 2014 and 2020. The incidence of POSI was significantly lower after secondary (12%) compared with primary (28%, p = 0.0084) surgery. In a multivariate analysis adjusting for tumour histology, the odds ratio for developing POSI after secondary surgery was 0.23, compared with primary surgery (95% confidence interval: 0.08-0.65, p = 0.006). The frequency of postoperative CND did not differ significantly after primary vs. secondary surgery (p = 0.21).

conclusionChildren have a lower risk of POSI after secondary than after primary surgery for posterior fossa tumours but remain at significant risk of both POSI and CND. The present findings should be taken in account when weighing risks and benefits of secondary surgery for posterior fossa tumours.

Indexed as

Cerebellar NeoplasmsInfratentorial NeoplasmsMutismChildCranial Fossa, PosteriorCranial NervesHumansNeoplasm Recurrence, LocalPostoperative ComplicationsProspective StudiesSpeechCerebellar mutism syndromePosterior fossa syndromePosterior fossa tumourSecondary resection

Identifiers

PMID35157109
OpenAlexW4212869872

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.