Evidence map›Paper›PMID 40767023›Full record

ArticleEpilepsia open2025

What determines the timing of epilepsy surgery in children with cortical malformations and low-grade epilepsy-associated tumors?

Maurits W C B Sanders, Matyas Ebel, Aswin Chari, Merel Fleumer, Anca M Vasilica, Maria H Eriksson, Martin Tisdall, Barbora Splitkova, Anezka Belohlavkova, Willem M Otte and 4 more

Abstract readMulticenter Study
In one paragraph

Article in Epilepsia open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

14 authors.

Maurits W C B SandersDepartment of Child Neurology, Brain Center, University Medical Center, Utrecht, The Netherlands.ORCID https://orcid.org/0000-0003-0592-1098
Matyas EbelDepartment of Paediatric Neurology, Motol Epilepsy Center, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.ORCID https://orcid.org/0000-0002-4795-152X
Aswin ChariUCL NIHR BRC Great Ormond Street Institute of Child Health and Great Ormond Street Hospital for Children, London, UK.
Merel FleumerDepartment of Child Neurology, Brain Center, University Medical Center, Utrecht, The Netherlands.
Anca M VasilicaUCL NIHR BRC Great Ormond Street Institute of Child Health and Great Ormond Street Hospital for Children, London, UK.
Maria H ErikssonUCL NIHR BRC Great Ormond Street Institute of Child Health and Great Ormond Street Hospital for Children, London, UK.ORCID https://orcid.org/0000-0001-6869-5804
Martin TisdallUCL NIHR BRC Great Ormond Street Institute of Child Health and Great Ormond Street Hospital for Children, London, UK.
Barbora SplitkovaDepartment of Paediatric Neurology, Motol Epilepsy Center, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.ORCID https://orcid.org/0000-0002-3462-7421
Anezka BelohlavkovaDepartment of Paediatric Neurology, Motol Epilepsy Center, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Willem M OtteDepartment of Child Neurology, Brain Center, University Medical Center, Utrecht, The Netherlands.ORCID https://orcid.org/0000-0003-1511-6834
Floor E JansenDepartment of Child Neurology, Brain Center, University Medical Center, Utrecht, The Netherlands.
J Helen CrossUCL NIHR BRC Great Ormond Street Institute of Child Health and Great Ormond Street Hospital for Children, London, UK.ORCID https://orcid.org/0000-0001-7345-4829
Kees P J BraunDepartment of Child Neurology, Brain Center, University Medical Center, Utrecht, The Netherlands.
Pavel KrsekDepartment of Paediatric Neurology, Motol Epilepsy Center, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.

Funding

Ministry of Health of the Czech Republic in cooperation with the Czech Health Research Council NU21J-08-00081NIHR Great Ormond Street Hospital Biomedical Research Centre
6 · The paper itself

Abstract

objectivesTimely referral and efficient presurgical evaluation are important to optimize postoperative seizure and developmental outcomes in epilepsy surgery patients. We aimed to identify determinants of time intervals from epilepsy diagnosis to referral to specialized centers and epilepsy surgery in children with malformations of cortical development (MCDs) and low-grade epilepsy-associated tumors (LEATs).

methodsWe performed a retrospective cohort study in 3 European centers, including children with MCD or LEAT who underwent epilepsy surgery between 2010 and 2020. Primary endpoints were (1) time interval between epilepsy diagnosis and referral for presurgical evaluation, (2) duration of presurgical evaluation trajectory, and (3) time from diagnosis to surgery. The secondary endpoint was postoperative seizure outcome. In our primary analysis, we performed a multivariable Cox proportional hazards analysis and used histopathological diagnosis, age at first seizure, presence of developmental delay, 1st seizure classification, initial EEG and MRI findings, duration until drug resistance, and family history as covariates.

resultsOf the 507 children included, 259 (51%) had an MCD and 248 (49%) had a LEAT. Earlier drug resistance and the presence of an MR-visible epileptogenic lesion were associated with shorter times from diagnosis to referral and surgery, and later onset of seizures was associated with a shorter time to surgery. LEAT was associated with a shorter presurgical evaluation and shorter time to surgery. An older age at surgery, shorter time from diagnosis to surgery, and a histopathological diagnosis of FCDII and LEAT were all independently associated with better postoperative seizure outcome. SIGNIFICANCE: Epilepsy surgery was performed earlier in children with MR-visible lesions and early drug resistance, particularly those with LEAT, and a shorter duration to epilepsy surgery was associated with better seizure outcomes. Many patients were initially considered MRI-negative in the referring center, highlighting the importance of early referral, epilepsy-dedicated MRI protocols, and experienced neuroradiologists. Increasing awareness of timely referral and surgery benefits is crucial for improving outcomes. PLAIN LANGUAGE SUMMARY: Children with severe focal structural epilepsy who have not responded to medication often benefit from surgery, especially when they are referred early. This study of 507 children found that certain factors-such as visible brain abnormalities on the first MRI, especially a specific type of brain tumor (LEAT), early signs of drug resistance, and seizures starting later in childhood-were linked to shorter times from diagnosis to surgery and that shorter time to surgery was linked to better seizure outcomes. Many children whose initial MRIs appeared to be normal were later found to have an epileptogenic brain lesion when examined at specialized centers. Early referral, advanced imaging, and expert evaluation are key to improving postsurgical outcomes.

Indexed as

Brain NeoplasmsEpilepsyMalformations of Cortical DevelopmentNeurosurgical ProceduresTime-to-TreatmentAdolescentChildChild, PreschoolCohort StudiesDrug Resistant EpilepsyElectroencephalographyFemaleHumansInfantMagnetic Resonance ImagingMaleepilepsy surgeryLEATMCDMRItiming

Identifiers

PMID40767023
PMCPMC12514363

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