Evidence map›Paper›PMID 39636170›Full record

ArticleEpilepsia2025

Epilepsy surgery in children with operculoinsular epilepsy: Results of a large unicentric cohort.

Martin Kudr, Radek Janca, Alena Jahodova, Anezka Belohlavkova, Matyas Ebel, Katerina Bukacova, Alice Maulisova, Michal Tichy, Petr Liby, Martin Kyncl and 7 more

Abstract read
In one paragraph

Article in Epilepsia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Beyond Broca and Wernicke: Epilepsy surgery in the language areas.Epileptic disorders : international epilepsy journal with videotape · 2026
    Review
  4. Article
  5. 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

17 authors.

Martin KudrDepartment of Paediatric Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.ORCID https://orcid.org/0000-0001-7853-3446
Radek JancaEpilepsy Research Centre Prague-EpiReC Consortium, Prague, Czech Republic.ORCID https://orcid.org/0000-0003-0825-1069
Alena JahodovaDepartment of Paediatric Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Anezka BelohlavkovaDepartment of Paediatric Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Matyas EbelDepartment of Paediatric Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Katerina BukacovaDepartment of Paediatric Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Alice MaulisovaDepartment of Paediatric Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Michal TichyEuropean Reference Network EpiCARE, Prague, Czech Republic.
Petr LibyEuropean Reference Network EpiCARE, Prague, Czech Republic.
Martin KynclEuropean Reference Network EpiCARE, Prague, Czech Republic.
Zuzana HolubovaEuropean Reference Network EpiCARE, Prague, Czech Republic.
Jan SandaEuropean Reference Network EpiCARE, Prague, Czech Republic.
Petr JezdikEpilepsy Research Centre Prague-EpiReC Consortium, Prague, Czech Republic.ORCID https://orcid.org/0000-0001-8932-0497
Katerina MackovaEpilepsy Research Centre Prague-EpiReC Consortium, Prague, Czech Republic.
Gonzalo Alonso Ramos RiveraDepartment of Pediatrics, Jessenius Medical Faculty, Comenius University and University Hospital Martin, Martin, Slovakia.ORCID https://orcid.org/0009-0003-4184-0321
Luka KopacDepartment of Pediatrics, General Hospital Celje, Celje, Slovenia.
Pavel KrsekDepartment of Paediatric Neurology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.

Funding

Charles University Grant Agency 666320Czech Science Foundation 20-21339SERDF-Project Brain Dynamics CZ.02.01.01/00/22_008/0004643EU Next Generation project X22NPO5107 NEUR-inGrant Agency of the Czech Technical University in Prague SGS23/170/OHK3/3T/13Ministry of Health of the Czech Republic 00064203Ministry of Health of the Czech Republic NU23-08-00528
6 · The paper itself

Abstract

objectiveEpilepsy surgery in the operculoinsular cortex is challenging due to the difficult delineation of the epileptogenic zone and the high risk of postoperative deficits.

methodsPre- and postsurgical data from 30 pediatric patients who underwent operculoinsular cortex surgery at the Motol Epilepsy Center Prague from 2010 to 2022 were analyzed.

resultsFocal cortical dysplasia (FCD; n = 15, 50%) was the predominant cause of epilepsy, followed by epilepsy-associated tumors (n = 5, 17%) and tuberous sclerosis complex (n = 2, 7%). In eight patients where FCD was the most likely etiology, the histology was negative. Seven patients (23%) displayed normal magnetic resonance imaging results. Seizures exhibited diverse semiology and propagation patterns (frontal, perisylvian, and temporal). The ictal and interictal electroencephalographic (EEG) findings were mostly extensive. Multimodal imaging and advanced postprocessing were frequently used. Stereo-EEG was used for localizing the epileptogenic zone and eloquent cortex in 23 patients (77%). Oblique electrodes were used as guides for better neurosurgeon orientation. The epileptogenic zone was in the dominant hemisphere in 16 patients. At the 2-year follow-up, 22 patients (73%) were completely seizure-free, and eight (27%) experienced a seizure frequency reduction of >50% (International League Against Epilepsy class 3 and 4). Fourteen patients (47%) underwent antiseizure medication tapering; treatment was completely withdrawn in two (7%). Nineteen patients (63%) remained seizure-free following the definitive outcome assessment (median = 6 years 5 months, range = 2 years to 13 years 5 months postsurgery). Six patients (20%) experienced corona radiata or basal ganglia ischemia; four (13%) improved to mild and one (3%) to moderate hemiparesis. Two patients (7%) operated on in the anterior insula along with frontotemporal resection experienced major complications: pontine ischemia and postoperative brain edema. SIGNIFICANCE: Epilepsy surgery in the operculoinsular cortex can lead to excellent patient outcomes. A comprehensive diagnostic approach is crucial for surgical success. Rehabilitation brings a great chance for significant recovery of postoperative deficits.

Indexed as

Epilepsy, Frontal LobeNeurosurgical ProceduresAdolescentChildChild, PreschoolCohort StudiesElectroencephalographyFemaleHumansMagnetic Resonance ImagingMaleMalformations of Cortical DevelopmentTreatment OutcomeTuberous Sclerosisepilepsy surgerymultimodal imagingopercular–insular epilepsypartial‐volume effect correctionPETSEEGSISCOM

Identifiers

PMID39636170
PMCPMC11827755

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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.