Frontal-onset absences in children: associated with worse outcome? A replication study
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Published on: December 2, 2015
Bosanka Jocić-Jakubi1, Marina Jovanović, Dojranka Stanković Janković
1Pediatric Clinic, Medical School, University of Nis, Nis, Serbia.
Insights
Childhood absence epilepsy with frontal onset may be a distinct subtype. These children often experience complex seizures and more behavioral issues, sometimes requiring additional medication beyond valproate.
Area of Science:
- Neurology
- Pediatric Neurology
- Epileptology
Background:
- Childhood absence epilepsy (CAE) is a common epilepsy syndrome in children.
- EEG patterns are crucial for diagnosing and classifying CAE.
- Frontal onset seizures in CAE may represent a unique clinical entity.
Purpose of the Study:
- To investigate the clinical and electroencephalographic (EEG) features of children with CAE.
- To compare children with classical absence seizures versus those with frontal onset epileptic abnormalities.
- To identify potential differences in treatment response and associated problems between these groups.
Main Methods:
- Retrospective analysis of 30 children diagnosed with CAE.
- Classification into two groups based on EEG patterns: classical absence (Group A) and frontal onset (Group B).
- Evaluation of clinical features, seizure types, EEG findings, treatment response, and learning/behavioral problems.
Main Results:
- Group B (frontal onset) showed more complex absences compared to Group A.
- While most children responded to valproate, 3 in Group B required ethosuximide for seizure freedom.
- The frontal group exhibited a higher prevalence of learning and behavioral problems.
Conclusions:
- Frontal onset absences appear to be a specific subtype of childhood absence epilepsy.
- This subtype may be associated with more complex seizure presentations and greater learning/behavioral challenges.
- Findings support and largely confirm previous research on frontal onset absences in children.
Abstract:
We studied the clinical and electroencephalographic features in 30 children who were diagnosed with childhood absence epilepsy. According to their EEG pattern we divided the 30 children into two groups: group A: 11 children with classical absences whose ictal EEG showed primary generalized spikes and waves and group B: 19 children with frontal onset of the EEG epileptic abnormalities ('frontal group'). In the frontal group, more frequently complex absences were seen. Although the majority of children responded very well to valproate monotherapy, ethosuximide has to be added in 3 children of the frontal group to achieve seizure freedom. In the frontal group, also more learning and behavioural problems were encountered. This study largely confirms a previous study of Lagae et al. [Lagae L, Pauwels J, Monte B, Verhelle J, Vervisch J. Frontal absences in children. Eur J Pediatr Neurol 2001;5:243-251]. It seems that frontal onset absences constitute a specific subtype within the childhood absence epilepsies.
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