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Seizure Freedom in Children With Pathology-Confirmed Focal Cortical Dysplasia
Anna Mrelashvili1, Robert J Witte2, Elaine C Wirrell1
1Division of Child and Adolescent Neurology, Mayo Clinic, Rochester, Minnesota.
Insights
Children with focal cortical dysplasia who underwent surgery achieved sustained seizure freedom more often when older at seizure onset and surgery, and with mild intellectual disability. These factors predict long-term seizure control after epilepsy surgery.
Area of Science:
- Pediatric Neurology
- Epilepsy Surgery
- Neuroscience
Background:
- Focal cortical dysplasia (FCD) is a leading cause of drug-resistant focal epilepsy in children.
- Resective surgery offers a potential cure for epilepsy in select pediatric patients.
- Understanding predictors of long-term seizure control is crucial for surgical decision-making.
Purpose of the Study:
- To evaluate the temporal course of seizure outcomes in children with FCD after resective surgery.
- To identify clinical predictors associated with sustained seizure freedom in this population.
Main Methods:
- Retrospective single-center study of pediatric patients (≤ 18 years) with pathology-confirmed FCD who underwent resective surgery.
- Surgical outcomes classified as seizure freedom (Engel class I) or recurrence (Engel classes II-IV).
- Survival analysis used to assess time to seizure recurrence and cumulative seizure-free rates.
Main Results:
- Of 38 patients, 53% achieved seizure freedom and 68% had at least 3 months of seizure freedom.
- Median time to seizure recurrence was 38 months.
- Older age at seizure onset, older age at surgery, and absent/mild intellectual disability predicted sustained seizure freedom.
Conclusions:
- Older age at seizure onset and surgery are favorable predictors for sustained seizure freedom in pediatric FCD.
- Absence or mild intellectual disability is also associated with better long-term seizure control post-surgery.
- Achieving initial seizure freedom for at least 3 months is a strong predictor of sustained seizure freedom.
Objective:
We evaluated the temporal course of seizure outcome in children with pathology-confirmed focal cortical dysplasia and explored predictors of sustained seizure freedom.
Methods:
We performed a single-center retrospective study of children ≤ 18 years who underwent resective surgery from January 1, 2000 through December 31, 2012 and had pathology-proven focal cortical dysplasia. Surgical outcome was classified as seizure freedom (Engel class I) or seizure recurrence (Engel classes II-IV). Fisher exact and nonparametric Wilcoxon ranksum tests were used, as appropriate. Survival analysis was based on seizure-free outcome. Patients were censored at the time of seizure recurrence or seizure freedom at last follow-up.
Results:
Thirty-eight patients were identified (median age at surgery, 6.5 years; median duration of epilepsy, 3.3 years). Median time to last follow-up was 13.5 months (interquartile range, 7-41 months). Twenty patients (53%) were seizure free and 26 patients (68%) attained seizure freedom for a minimum of 3 months. Median time to seizure recurrence was 38 months (95% confidence interval, 6-109 months), and the cumulative seizure-free rate was 60% at 12 months (95% confidence interval, 43%-77%). Clinical features associated with seizure freedom at last follow-up included older age at seizure onset (P = .02), older age at surgery (P = .04), absent to mild intellectual disability before surgery (P = .05), and seizure freedom for a minimum of 3 months (P < .001).
Conclusion:
Favorable clinical features associated with sustained seizure freedom included older age at seizure onset, older age at surgery, absent or mild intellectual disability at baseline, and seizure freedom for a minimum of 3 months.
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