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Levetiracetam in continuous spike waves during slow-wave sleep syndrome
Shi-Bing Wang1, Wen-Chin Weng, Pi-Chuan Fan
1Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Insights
Levetiracetam effectively treats epilepsy with continuous spike waves during slow-wave sleep (CSWS) in children, reducing seizure frequency. However, young children may experience a high relapse rate of CSWS.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Neuroscience
Background:
- Epilepsy with continuous spike waves during slow-wave sleep (CSWS) is a rare epilepsy syndrome.
- Understanding the clinical presentation and treatment outcomes is crucial for effective management.
Purpose of the Study:
- To investigate the clinical characteristics of children diagnosed with CSWS.
- To evaluate the treatment response and relapse rates associated with levetiracetam in this pediatric population.
Main Methods:
- Retrospective review of clinical data for six children diagnosed with CSWS.
- Analysis of neuroimaging findings, seizure frequency, and response to levetiracetam.
- Monitoring for relapse of electrical status epilepticus during sleep pattern.
Main Results:
- The most common sign was increased seizure frequency (100%).
- Levetiracetam showed initial efficacy in five out of six children.
- A 40% relapse rate was observed in two 5-year-old children within 4-5 months.
Conclusions:
- Levetiracetam is an effective treatment for CSWS in children.
- Younger children with CSWS may have a higher risk of relapse, necessitating continued monitoring.
Abstract:
We investigated the clinical characteristics of children with continuous spike waves during slow-wave sleep syndrome and their treatment response to levetiracetam. Five boys and one girl, diagnosed with epilepsy with continuous spike waves during slow-wave sleep syndrome, were enrolled. Their clinical characteristics, including neuroimaging findings, were reviewed. The signs related to continuous spike waves during slow-wave sleep included increased seizure frequency (6/6), impaired responsiveness (3/6), and psychomotor regression (2/6). Magnetic resonance imaging disclosed lissencephaly in one patient, and porencephaly of the left hemisphere in another. The number of antiepileptic drugs before the use of levetiracetam was 0-4 (mean +/- SD, 2.3 +/- 1.5). Five of 6 children demonstrated a good response to levetiracetam, whereas 2 (40%) underwent a relapse of electrical status epilepticus during sleep pattern on electroencephalograms 4 and 5 months after clinical improvement. Both were 5 years old. The most common presenting sign in children with continuous spike waves during slow-wave sleep syndrome is increasing seizure frequency. Levetiracetam is effective in treating children with continuous spike waves during slow-wave sleep syndrome. However, the relapse rate of continuous spike waves during slow-wave sleep syndrome remains high in young children.
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