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Correlation Between Efficacy of Levetiracetam and Serum Levels Among Children With Refractory Epilepsy

机译:顽固性癫痫患儿左乙拉西坦的疗效与血清水平的相关性

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BACKGROUND: Levetiracetam is used as adjunctive therapy in various types of seizures. Studies evaluating the effect of levetiracetam on children with refractory epilepsy are scarce. The aim of this study was to evaluate the correlation between serum concentration of levetiracetam and either efficacy or tolerability in children with refractory epilepsy, and to determine the value of levetiracetam blood level monitoring. METHODS: Medical records of 50 children with refractory epilepsy treated with levetiracetam and regularly followed at Assaf Harofeh Medical Center were retrospectively reviewed. Trough serum levetiracetam concentration was determined using high-performance liquid chromatography and correlated with the administered dose and clinical report. RESULTS: No correlation between levetiracetam serum levels and clinical efficacy, tolerability or administered dosage was found. The average dose of levetiracetam was 43.7 +/- 20.0 (range 14-100) mg/kg/day and the average serum concentration was 16.0 +/- 9.5 (range 2.5-38.5) mu g/mL. Forty-five patients (95%) had more than a 50% reduction of seizure frequency, with 22 (44%) patients becoming seizure-free for at least 6 months. Adverse events related to levetiracetam were reported in 15 (30%) patients. No correlation between serum concentrations and adverse events was found. These results were not affected by gender, age, type of seizure, and other drugs. CONCLUSIONS: Determination of serum concentration is not needed in all children treated with levetiracetam. Serum concentrations may be valuable either in patients with refractory epilepsy for compliance evaluation or in patients with satisfactory control of seizures for determination of their therapeutic baseline.
机译:背景:左乙拉西坦在各种类型的癫痫发作中用作辅助治疗。评估左乙拉西坦对难治性癫痫患儿疗效的研究很少。这项研究的目的是评估左乙拉西坦的血清浓度与难治性癫痫患儿的疗效或耐受性之间的相关性,并确定左乙拉西坦血液水平监测的价值。方法:回顾性分析50例接受左乙拉西坦治疗的难治性癫痫患儿的医疗记录,并定期在阿萨夫·哈罗费医疗中心进行随访。使用高效液相色谱法测定低谷左乙拉西坦的浓度,并与给药剂量和临床报告相关。结果:左乙拉西坦血清水平与临床疗效,耐受性或给药剂量之间无相关性。左乙拉西坦的平均剂量为43.7 +/- 20.0(范围14-100)mg / kg /天,平均血清浓度为16.0 +/- 9.5(范围2.5-38.5)μg / mL。四十五名患者(95%)的癫痫发作频率降低了50%以上,其中22名患者(44%)的癫痫发作至少六个月无发作。 15(30%)位患者报告了与左乙拉西坦相关的不良事件。没有发现血清浓度和不良事件之间的相关性。这些结果不受性别,年龄,癫痫发作类型和其他药物的影响。结论:所有接受左乙拉西坦治疗的儿童均无需测定血清浓度。血清浓度对于难治性癫痫患者的依从性评估或在癫痫发作控制良好以测定治疗基线的患者中可能是有价值的。

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