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Benign epilepsy of childhood with rolandic spikes: typical and atypical variants
Anita Datta1, D Barry Sinclair
1Comprehensive Epilepsy Program, University of Alberta, Edmonton, Alberta, Canada.
Insights
Children with typical and atypical benign epilepsy of childhood with rolandic spikes (BECRS) show similar seizure freedom rates and long-term outcomes. Comorbidities were slightly more common in the atypical group.
Area of Science:
- Pediatric Neurology
- Epileptology
Background:
- Benign epilepsy of childhood with rolandic spikes (BECRS) is a common epilepsy syndrome in children.
- Distinguishing typical from atypical presentations is crucial for prognosis and management.
Purpose of the Study:
- To compare the clinical course and outcomes of children with typical versus atypical features of BECRS.
- To identify any differences in seizure control, medication requirements, and long-term prognosis between the two groups.
Main Methods:
- Retrospective case series design.
- Inclusion of 126 children diagnosed with BECRS at a tertiary-care pediatric hospital.
- Subdivision into typical (Group A) and atypical (Group B) features based on clinical presentation.
Main Results:
- Comorbid disorders, such as ADHD and behavioral problems, were slightly more frequent in the atypical BECRS group.
- No significant difference in time to seizure freedom was observed between groups; by two years, 62% of typical and 71% of atypical cases were seizure-free.
- Approximately 16% of children required a second anti-epileptic drug, with a slightly higher proportion in the atypical group.
- Resolution of epilepsy occurred over similar timeframes for both groups, with comparable long-term outcomes.
Conclusions:
- Typical and atypical presentations of BECRS exhibit similar seizure control rates and long-term outcomes.
- While comorbid conditions may be more prevalent in atypical cases, they do not appear to significantly alter the overall prognosis of BECRS.
Abstract:
Clinical course and outcome were compared for 126 children with typical and atypical features of benign epilepsy of childhood with rolandic spikes (BECRS). A retrospective case series design was used, in the setting of a tertiary-care pediatric hospital. The subjects were subdivided into two groups, based on clinical presentation. Group A comprised children with typical features of BECRS (n = 66; 52%) and Group B, those with atypical features (n = 60; 48%). Patients' charts were reviewed for demographic data, family history, comorbid conditions, atypical clinical features, anti-epileptic drugs, and outcome data. Comorbid disorders (e.g., attention deficit hyperactivity disorder, behavioral problems) were slightly more frequent in the atypical group. Overall, there was no difference between the time to become seizure free between the groups: by two years, 41 of 66 in Group A (62%) and 44 of 60 in Group B (71%) were controlled on medication and seizure free. Twenty of the 126 children (16%) required trial of a second anti-epileptic drug: 7 in Group A and 13 in Group B. Resolution of the epilepsy occurred in about the same length of time in both groups (but at different ages, consistent with different age of onset). Both groups had similar long-term outcome.
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