Journal article
Outcomes of Early-Life Focal Cortical Dysplasia-Related Epilepsy: A PERC Surgery Study
Neurology. Clinical practice, Vol.15(6), e200539
12/2025
DOI: 10.1212/CPJ.0000000000200539
PMCID: PMC12507445
PMID: 41070137
Abstract
Focal cortical dysplasia (FCD) is the most common cause of surgically treatable drug-resistant epilepsy (DRE) in children. Surgical outcomes are poorly defined in early-onset FCD-DRE. The purpose of this study was to evaluate clinical and presurgical characteristics relating to surgical outcomes in early-life (seizure onset <4 months old) FCD-DRE.
A multicenter prospective cohort was analyzed from the Pediatric Epilepsy Research Consortium (PERC) Surgery Database to identify patients with pathologically confirmed FCD-DRE and seizure onset younger than 4 months old. Clinical characteristics, presurgical workup, and surgical intervention and outcomes data were collected and analyzed. Primary outcome was to evaluate whether earlier surgery is associated with seizure freedom; secondary outcomes evaluated clinical/presurgical predictors of seizure freedom and safety.
Thirty-one patients with FCD-DRE were identified from 18 PERC centers. Median age at seizure onset was 2.4 months (interquartile range 1.2-3.6 months). Four patients had focal to bilateral tonic-clonic seizures (FBTCS); 35% (n = 11) had epileptic spasms. Median age at phase 1 referral was 2.0 years (0.7-4.0 years). Median age at surgery was 2.6 years (1.1-5.5 years). Pathology was type II, 65% (n = 20); type I, 26% (n = 8); and type III, 6% (n = 2). Seizure freedom was achieved in 65% (n = 20) with median follow-up 2.5 years (1.3-4 years). Age at seizure onset/referral/surgery, surgery type, and experiencing FBTCS were not associated with seizure-free outcome. Type IIB pathology had 89% (n = 8) seizure-free outcome. Epileptic spasms had 45% seizure-free outcome. Transient neurologic deficits occurred in 2 patients, and an expected neurologic deficit in 1 (visual field cut from occipital lobectomy). There were no deaths.
This study finds high rates of seizure-free outcome in epilepsy surgery for early-onset FCD-DRE across all pathologies and procedures with minimal complication rates and no deaths. Focal cortical dysplasia type IIB is associated with very high rates of seizure-free outcome. Epileptic spasms were associated with lower seizure-free outcome. The study also fails to confirm a high rate of multilobar unilateral hypoplasia with severe epilepsy in children, a type I FCD variant that has been reported as a common etiology of early-life FCD.
Details
- Title: Subtitle
- Outcomes of Early-Life Focal Cortical Dysplasia-Related Epilepsy: A PERC Surgery Study
- Creators
- Nathan T Cohen - George Washington University HospitalDewi Frances Depositario-Cabacar - George Washington University HospitalChima O Oluigbo - George Washington University HospitalAdam P Ostendorf - Nationwide Children's HospitalLily Wong-Kisiel - Mayo ClinicErin Fedak Romanowski - Michigan MedicineNancy A McNamara - C. S. Mott Children's HospitalPriyamvada Tatachar - Northwestern UniversityKrista Eschbach - Children's Hospital ColoradoAllyson L Alexander - Children's Hospital ColoradoPilar D Pichon - Children's Hospital of Orange CountyMichael A Ciliberto - University of IowaErnesto Gonzalez-Giraldo - University of California, San FranciscoDanilo Bernardo - University of California, San FranciscoKurtis I Auguste - University of California, San FranciscoJason Coryell - Oregon Health & Science UniversityKristen H Arredondo - The University of Texas at AustinEdward John Novotny - University of WashingtonShilpa B Reddy - Monroe Carell Jr. Children's HospitalAbhinaya Ganesh - Monroe Carell Jr. Children's HospitalAhmad Marashly - Johns Hopkins UniversityPradeep K Javarayee - Medical College of WisconsinRani K Singh - Wake Forest UniversityJeffrey Brian Bolton - Boston Children's MuseumZachary M Grinspan - Weill Cornell MedicineSamir Karia - University of LouisvilleCemal Karakas - University of LouisvilleJenny Lin - Children's Healthcare of AtlantaAndrew T Knox - University of Wisconsin–MadisonSteven M Wolf - Maria Fareri Children's HospitalTaylor J Abel - University of PittsburghDebopam Samanta - University of Arkansas for Medical SciencesDallas Michael Armstrong - The University of Texas Southwestern Medical CenterSpriha Pavuluri - Children's Hospital & Medical CenterAnn Hyslop - Stanford UniversityFernando N Galan - Nemours Children's Health SystemDerryl J Miller - Indiana University – Purdue University IndianapolisJason S Hauptman - Phoenix Children's HospitalAvery Robert Caraway - Cook Children's Medical CenterM Scott Perry - Cook Children's Medical CenterWilliam D Gaillard - George Washington University Hospital
- Resource Type
- Journal article
- Publication Details
- Neurology. Clinical practice, Vol.15(6), e200539
- DOI
- 10.1212/CPJ.0000000000200539
- PMID
- 41070137
- PMCID
- PMC12507445
- NLM abbreviation
- Neurol Clin Pract
- ISSN
- 2163-0402
- eISSN
- 2163-0933
- Publisher
- LIPPINCOTT WILLIAMS & WILKINS
- Grant note
- Cook Children's Medical Center
The authors acknowledge the Pediatric Epilepsy Research Consortium (PERC) members who provided patient information to the database and helped contribute to this paper. The authors also acknowledge the Cook Children's Medical Center for funding and housing the PERC Surgery database.
- Language
- English
- Date published
- 12/2025
- Academic Unit
- Neurology; Stead Family Department of Pediatrics; Neurology (Pediatrics)
- Record Identifier
- 9985014876202771
Metrics
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