Evidence map›Paper›PMID 39871521›Full record

ArticleEpilepsia2025

Stereoelectroencephalographic exploration and surgical outcome in Lennox-Gastaut syndrome.

Soomi Cho, Julia Makhalova, Samuel Medina Villalon, Nathalie Villeneuve, Agnes Trébuchon, Manel Krouma, Didier Scavarda, Anne Lépine, Mathieu Milh, Romain Carron and 6 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Observational
  2. Review
  3. Radiofrequency thermocoagulation for the treatment of refractory focal status epilepticus.Epileptic disorders : international epilepsy journal with videotape · 2025
    Article
  4. Article
  5. Article
  6. 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

16 authors.

Soomi ChoDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.ORCID https://orcid.org/0000-0003-4723-8975
Julia MakhalovaDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.ORCID https://orcid.org/0000-0001-7962-2942
Samuel Medina VillalonDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.
Nathalie VilleneuveDepartment of Pediatric Neurology, APHM, Timone Hospital, Marseille, France.
Agnes TrébuchonDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.
Manel KroumaDepartment of Pediatric Neurosurgery, APHM, Timone Hospital, Marseille, France.
Didier ScavardaDepartment of Pediatric Neurosurgery, APHM, Timone Hospital, Marseille, France.ORCID https://orcid.org/0000-0001-9344-8071
Anne LépineDepartment of Pediatric Neurology, APHM, Timone Hospital, Marseille, France.
Mathieu MilhDepartment of Pediatric Neurology, APHM, Timone Hospital, Marseille, France.ORCID https://orcid.org/0000-0002-2454-8543
Romain CarronDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.
Francesca BoniniDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.
Géraldine DaquinDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.
Sandrine AubertDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.
Stanislas LagardeDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.ORCID https://orcid.org/0000-0003-2916-1302
Francesca PizzoDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.ORCID https://orcid.org/0000-0001-6345-1288
Fabrice BartolomeiDepartment of Epileptology and Cerebral Rhythmology, APHM, Timone Hospital, Marseille, France.ORCID https://orcid.org/0000-0002-1678-0297

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveLennox-Gastaut syndrome (LGS) is typically characterized by drug-resistant epilepsy and subsequent cognitive deterioration. Surgery is a rare but viable option for the control of seizures in a subset of patients with LGS. This study aimed to describe the organization of the epileptogenic zone network (EZN) in patients with LGS using stereoelectroencephalography (SEEG) and to report the outcome of post-SEEG treatment.

methodsA quantitative SEEG signal analysis was conducted in 14 consecutive patients with LGS, in whom a potentially localized EZN was suggested based on a comprehensive noninvasive evaluation. The EZN and the irritative zone network were identified using relevant biomarkers during ictal (epileptogenicity index and connectivity epileptogenicity index) and interictal (spikes and high-frequency oscillations) recordings. The applied post-SEEG treatments were assessed, including SEEG-guided radiofrequency thermocoagulation (RF-TC), surgery, and neurostimulation.

resultsThe seizure onset patterns showed some specificity by seizure type, with 84% of tonic seizures involving low-voltage fast activity. The EZN of patients with LGS was often, but not always, complex and extensive, involving two or more lobes (79%) and both hemispheres (64%). The lateral neocortical structures, particularly the lateral premotor and dorsolateral prefrontal cortices, were identified as being most frequently involved in the EZN. Among the explored subcortical structures, only the pulvinar, central-lateral thalamic nucleus, and hypothalamic hamartoma belonged to the EZN. Twelve patients (86%) underwent SEEG-guided RF-TC, with 50% experiencing a >50% reduction in baseline seizure frequency. Four patients (29%) underwent curative surgery for significant involvement of a lesion in the EZN, and one case achieved an Engel class I outcome. SIGNIFICANCE: This is the first quantitative SEEG study in patients with LGS to demonstrate the utility of SEEG in identifying patients who may benefit from surgery and to perform SEEG-guided RF-TC. Nevertheless, the indications for SEEG should be carefully assessed, as localized EZN is uncommon in LGS.

Indexed as

ElectroencephalographyLennox Gastaut SyndromeStereotaxic TechniquesAdolescentAdultChildChild, PreschoolElectrocoagulationFemaleHumansMaleTreatment OutcomeYoung AdultepileptogenicityLGSpost‐SEEG outcomeepileptogenic zoneSEEG

Identifiers

PMID39871521
PMCPMC12097472

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Registered trials

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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.