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Published on: September 20, 2024
Efficacy and tolerability of levetiracetam in children with epilepsy
Jiahui Li1, Nong Xiao, Siyuan Chen
1Department of Rehabilitation Center, Children's Hospital of Chongqing Medical University, China.
Insights
Levetiracetam (Lev) demonstrated significant efficacy and good tolerability in pediatric epilepsy patients. Most children achieved seizure freedom or reduction, with a high retention rate indicating its safety and effectiveness.
Area of Science:
- Pediatric Neurology
- Clinical Pharmacology
Background:
- Epilepsy affects a significant number of children worldwide.
- Levetiracetam is an antiepileptic drug with a broad spectrum of action.
- Assessing its use in pediatric populations is crucial for treatment optimization.
Purpose of the Study:
- To evaluate the efficacy of levetiracetam in treating pediatric epilepsy.
- To assess the tolerability and safety profile of levetiracetam in children.
- To determine the retention rate and reasons for withdrawal in this cohort.
Main Methods:
- An open-label, prospective, single-arm, non-interventional study.
- 120 pediatric patients (≤14 years) with epilepsy were enrolled.
- Levetiracetam dosage was initiated at 10mg/kg/day, titrated up to a maximum of 60mg/kg/day, with seizure control and side effects monitored.
Main Results:
- 64.8% of patients achieved seizure freedom, and 83.0% experienced ≥50% seizure reduction.
- Common side effects included somnolence and nervousness, with an overall incidence rate of 47.5%.
- The one-year retention rate was 73.3%, with poor efficacy being the primary reason for withdrawal.
Conclusions:
- Levetiracetam appears to be a safe and effective antiepileptic drug for various seizure types in children.
- The drug shows a favorable efficacy and tolerability profile in pediatric epilepsy management.
- Further research can explore long-term outcomes and specific epilepsy syndromes in children treated with levetiracetam.
Objective:
To assess the efficacy and tolerability of levetiracetam (Lev) in children with epilepsy.
Methods:
Open-label observational, prospective, single arm, non-interventional study examining patients (≤14 years) with epilepsy, receiving mono- or combination therapy with levetiracetam. Levetiracetam was started at a dose of approximately 10mg/kg/day. The dose was titrated up with 10mg/kg increments if seizures were poorly controlled but the maximum daily dose could not be more than 60 mg/kg/day. Documented were seizure type and frequency, levetiracetam dose and side effects.
Results:
120 patients (39.3% females, mean age 4.5 ± 3.9 years) were enrolled. Average duration of follow-up was 10.3 ± 3.5 months. At study endpoint, 64.8% of patients got seizure free and 83.0% got a seizure reduction of ≥50%. Observed side effects were somnolence, dysphoria, nervousness, dystrophy, somnipathy, asitia, debilitation, etc. and the incidence rate in the study was 47.5%. Four (3.3%) of 120 patients withdrew because of intolerance of side effects. The estimated one year retention rate of levetiracetam was 73.3%. Poor effect was the most common reason for withdrawal.
Conclusions:
In our study, it seemed that levetiracetam was safe and effective for a wide range of epileptic seizures in children with epilepsy.
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