TY - JOUR
T1 - Pediatric epilepsy surgery
T2 - Global survey of referral and presurgical evaluation practices
AU - Ramantani, Georgia
AU - Cross, J Helen
AU - Cserpan, Dorottya
AU - Ahemad, Emtnan
AU - Aparicio, Javier
AU - Arzimanoglou, Alexis
AU - Barba, Carmen
AU - Bingaman, William
AU - Braun, Kees
AU - Burman, Richard J
AU - Butler, James
AU - Cai, Lixin
AU - Cao, Dezhi
AU - Caraballo, Roberto
AU - Chipaux-Raffo, Mathilde
AU - Cloppenborg, Thomas
AU - Cukiert, Arthur
AU - Cukiert, Cristine Mella
AU - Dal, Sameer
AU - Englot, Dario
AU - Enright, Noelle
AU - Fallah, Aria
AU - Ferrand Sorbets, Sarah
AU - Feucht, Martha
AU - Gill, Deepak
AU - Guio Mahecha, Laura
AU - Hadjinicolaou, Aris
AU - Hallböök, Tove
AU - Harvey, A Simon
AU - Holthausen, Hans
AU - Jiang, Yuwu
AU - Kannan, Lakshminarayanan
AU - Katlowitz, Kalman A
AU - Kotulska-Jóźwiak, Katarzyna
AU - Kudr, Martin
AU - Lallas, Matt
AU - Valappil, Ahsan Moosa Naduvil
AU - Patil, Sandeep Bhagwan
AU - Pieper, Tom
AU - Specchio, Nicola
AU - Tripathi, Manjari
AU - Vendegh, Lejla
AU - Weiner, Howard
AU - Wilmshurst, Jo
AU - Smith, Mary Lou
AU - Wirrell, Elaine
N1 - Publisher Copyright:
© 2026 The Author(s). Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.
PY - 2026/8
Y1 - 2026/8
N2 - Objective: Pediatric epilepsy surgery is well established, but contemporary global data on referral and presurgical evaluation practices are lacking. This International League Against Epilepsy (ILAE) Pediatric Epilepsy Surgery Task Force study provides an updated overview of current trends and regional differences. Methods: Group-level data were collected from 61 epilepsy surgery programs (49 pediatric-only) across 29 countries and six continents, identified through ILAE networks, and included all children and adolescents treated in 2023 who underwent presurgical evaluation/epilepsy surgery. Results: Group-level data were available for 2427 patients. Mean age at surgery was 9.1 ± 4.9 years; mean epilepsy duration was 5.3. At surgery, 3.2% were <1 year old (highest in Oceania: 5.1%), and 6.1% were nonpharmacoresistant (highest in Europe: 15.0%). Prior neurosurgery was reported in 14.2% (highest in North America: 28.8%), including 8.0% resections (6.1% for epilepsy, 1.5% for tumors; highest in Oceania: 16.5%), 2.3% disconnections (1.3% corpus callosotomy; highest in South America: 4.7%), and 4.2% neuromodulation (3.7% vagal nerve stimulation,.2% responsive neurostimulation, one deep brain stimulation; highest in North America: 12.2%). Developmental and epileptic encephalopathies (DEEs) at surgery included Lennox–Gastaut syndrome (7.4%), infantile epileptic spasms syndrome (5.1%), and DEE with spike–wave activation in sleep (1.5%). Presurgical investigations included fluorodeoxyglucose positron emission tomography (52.6%; highest in Oceania: 79.7%), genetic testing (46.8%; highest in Asia: 54.3%), magnetic resonance imaging (MRI) postprocessing (32.4%; highest in South America: 53.0%), functional MRI (fMRI; 15.2%; highest in North America: 40.3%), magnetoencephalography (11.9%; highest in North America: 39.3%), single photon emission computed tomography (9.6%; highest in North America: 22.2%), high-density electroencephalography (EEG; 1.9%; highest in Europe: 4.7%), source localization (1.6%; highest in Oceania: 7.6%), Wada test (1.2%; highest in North America: 3.5%), and EEG-fMRI (.5%; highest in Europe: 1.1%). Significance: Despite some early surgeries, including in infancy and before pharmacoresistance, mean epilepsy duration before surgery remains >5 years. Reoperations are common, with resection more frequent than neuromodulation. Genetic testing in nearly half of patients reflects its growing relevance, and the high rate of DEEs underscores the complexity of surgical candidates.
AB - Objective: Pediatric epilepsy surgery is well established, but contemporary global data on referral and presurgical evaluation practices are lacking. This International League Against Epilepsy (ILAE) Pediatric Epilepsy Surgery Task Force study provides an updated overview of current trends and regional differences. Methods: Group-level data were collected from 61 epilepsy surgery programs (49 pediatric-only) across 29 countries and six continents, identified through ILAE networks, and included all children and adolescents treated in 2023 who underwent presurgical evaluation/epilepsy surgery. Results: Group-level data were available for 2427 patients. Mean age at surgery was 9.1 ± 4.9 years; mean epilepsy duration was 5.3. At surgery, 3.2% were <1 year old (highest in Oceania: 5.1%), and 6.1% were nonpharmacoresistant (highest in Europe: 15.0%). Prior neurosurgery was reported in 14.2% (highest in North America: 28.8%), including 8.0% resections (6.1% for epilepsy, 1.5% for tumors; highest in Oceania: 16.5%), 2.3% disconnections (1.3% corpus callosotomy; highest in South America: 4.7%), and 4.2% neuromodulation (3.7% vagal nerve stimulation,.2% responsive neurostimulation, one deep brain stimulation; highest in North America: 12.2%). Developmental and epileptic encephalopathies (DEEs) at surgery included Lennox–Gastaut syndrome (7.4%), infantile epileptic spasms syndrome (5.1%), and DEE with spike–wave activation in sleep (1.5%). Presurgical investigations included fluorodeoxyglucose positron emission tomography (52.6%; highest in Oceania: 79.7%), genetic testing (46.8%; highest in Asia: 54.3%), magnetic resonance imaging (MRI) postprocessing (32.4%; highest in South America: 53.0%), functional MRI (fMRI; 15.2%; highest in North America: 40.3%), magnetoencephalography (11.9%; highest in North America: 39.3%), single photon emission computed tomography (9.6%; highest in North America: 22.2%), high-density electroencephalography (EEG; 1.9%; highest in Europe: 4.7%), source localization (1.6%; highest in Oceania: 7.6%), Wada test (1.2%; highest in North America: 3.5%), and EEG-fMRI (.5%; highest in Europe: 1.1%). Significance: Despite some early surgeries, including in infancy and before pharmacoresistance, mean epilepsy duration before surgery remains >5 years. Reoperations are common, with resection more frequent than neuromodulation. Genetic testing in nearly half of patients reflects its growing relevance, and the high rate of DEEs underscores the complexity of surgical candidates.
KW - developmental and epileptic encephalopathies (DEEs)
KW - genetic testing
KW - neuromodulation
KW - pediatric epilepsy surgery
KW - presurgical evaluation
KW - reoperations
UR - https://www.scopus.com/pages/publications/105041064404
U2 - 10.1002/epi.70312
DO - 10.1002/epi.70312
M3 - Article
C2 - 42227967
SN - 0013-9580
VL - 67
SP - 4008
EP - 4024
JO - Epilepsia
JF - Epilepsia
IS - 8
ER -