Clinical value of subclinical seizures in children with focal epilepsy
Abel Velkey1, Zsuzsanna Siegler, József Janszky
1Epilepsy Center, Bethesda Children's Hospital, Bethesda Street 3, Budapest, Hungary.
Insights
Subclinical seizures (SCSs) are common in children with focal epilepsy, detected via scalp-EEG. These electrographic discharges often aid in diagnosing epilepsy, helping localize seizure origins and guide treatment decisions.
Area of Science:
- Neurology
- Pediatric Epilepsy
- Clinical Neurophysiology
Background:
- Subclinical seizures (SCSs) are electrographic discharges without clinical manifestations.
- Understanding SCSs in pediatric focal epilepsy is crucial for accurate diagnosis and management.
Purpose of the Study:
- To determine the frequency, characteristics, and diagnostic utility of SCSs detected by scalp-EEG in children with focal epilepsy.
- To assess the impact of SCSs on epilepsy evaluation and treatment.
Main Methods:
- Analysis of a long-term monitoring (LTM) database of 322 pediatric patients (<18 years) with focal epilepsy.
- Re-analysis of video-EEG data for all identified cases of SCSs.
Main Results:
- SCSs were identified in 18% (59/322) of children, with 15% having no clinical seizures during LTM.
- SCSs were associated with longer epilepsy duration and LTM duration.
- SCSs provided supplementary diagnostic value in 85% of cases, aiding seizure onset zone localization (53%) and influencing treatment (12%).
Conclusions:
- Scalp-EEG detected SCSs are a frequent and significant finding in pediatric focal epilepsy.
- SCSs should be considered in the epilepsy evaluation process, alongside clinical symptoms and other EEG data.
- This study represents the first assessment of SCSs recorded by scalp-EEG in this population.
Purpose:
Subclinical seizures (SCSs) are ictal electrographic discharges lacking clinical seizure signs or subjective symptoms. In this study, frequency, characteristics and diagnostic relevance of SCSs recorded by scalp-EEG were analyzed in a large population of children with focal epilepsy.
Methods:
Long-term monitoring (LTM) database of 322 consecutive patients <18 years with focal epilepsy were assessed. Video-EEG data of all children with SCS were re-analyzed.
Results:
Fifty-nine of 322 (18%) children showed SCS on scalp-EEG, nine (15%) of them had no clinical seizures during LTM. Duration of epilepsy (5.2 vs. 6.9 years; p=0.019) as well as length of LTM (2.8 vs. 3.6 days; p<0.001) were longer in children with SCS. Neither sex, age at onset, age at LTM, nor focus localization showed significant difference. In 85% of cases the presence of SCS had supplementary value during the diagnostic process. It assisted localizing the seizure onset zone in 53%, suggested multiple seizure onset zones in 20% and influenced antiepileptic drug therapy in 12% of cases.
Discussion:
Scalp-EEG SCS in children with focal epilepsy is a frequent and important phenomenon. Although our therapeutic decisions are usually based on interictal and ictal EEG data and clinical symptoms, SCS is also suggested to be considered during the epilepsy evaluation process. This is the first study assessing SCSs recorded by scalp-EEG.
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