Childhood absence epilepsy
Insights
Regular valproate treatment is key for childhood absence epilepsy (CAE). Posterior delta rhythm on EEG indicates a better prognosis, suggesting fewer patients will develop generalized tonic-clonic seizures.
Area of Science:
- Neurology
- Pediatric Epilepsy
Background:
- Childhood absence epilepsy (CAE) is a rare idiopathic generalized epilepsy in children.
- It has a strong genetic component and an estimated incidence of 6.3-8/100,000 children.
Purpose of the Study:
- To review medical and electroencephalographic (EEG) records of 50 Chinese children with CAE.
- To identify factors influencing the evolution to generalized tonic-clonic seizures (GTCS) and prognostic indicators.
Main Methods:
- Retrospective review of 50 Chinese children diagnosed with CAE.
- Analysis of demographic data, medical history, EEG findings, treatment, and seizure evolution.
Main Results:
- The mean age of onset was 6.9 years; 12% had a family history of epilepsy, and 22% had prior febrile convulsions.
- Valproate was the primary treatment; 32% evolved to GTCS, with irregular treatment and longer disease duration being significant risk factors.
- Posterior delta rhythm on EEG was observed in 6 patients, none of whom evolved to GTCS.
Conclusions:
- Regular valproate treatment is the preferred management for CAE.
- Posterior delta rhythm on EEG appears to be a favorable prognostic indicator for CAE patients.
Background:
Childhood absence epilepsy (CAE) is a relatively rare form of idiopathic generalized epilepsy, occurring in previously normal children with a strong genetic predisposition. The annual incidence of CAE has been estimated at 6.3/100,000 to 8/100,000 children aged 0-15 years.
Methods:
Medical and electroencephalographic records of 50 Chinese children with CAE were reviewed.
Results:
There were 22 males and 28 females. The age of onset ranged from 3 to 12 years with a mean of 6.9 +/- 2.4 years. Six children (12%) had positive familial epileptic history and 11 patients (22%) had a past history of febrile convulsion. Electroencephalographically, there were posterior delta rhythm (6/50), frontocentral (1/50), and centrotemporal (1/50) spikes in addition to the characteristic 3 Hz spike and wave complex. All patients received regular or irregular treatment with valproate. Sixteen patients (32%) evolved to generalized tonic-clonic seizure (GTCS) with a mean of 2.1 +/- 1.6 years of lag from stopping valproate. The patients with GTCS had significant late onset of age, a longer active period, and longer treatment duration than those without GTCS (p < 0.01). There were significantly more patients with irregular treatment evolving to GTCS than those with regular treatment (p < 0.01). None of the patients with posterior delta rhythm evolved to GTCS.
Conclusions:
Regular treatment with valproate is the modality of choice in the management of CAE. Posterior delta rhythm seems to be a good prognostic factor electroencephalographically.
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