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The clinical efficacy and safety of levetiracetam add-on therapy for child refractory epilepsy

机译:左乙拉西坦联合治疗儿童难治性癫痫的临床疗效和安全性

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OBJECTIVE: To investigate the clinical efficacy and safety of Levetiracetam (LEV) add-on therapy for child refractory epilepsy. PATIENTS AND METHODS: Levetiracetam add-on therapy was tested on 65 children who suffered refractory epilepsy, and clinical seizures. Electroencephalogram (EGG) changes and adverse reactions were observed in these children respectively in three, six and twelve months after the therapy. RESULTS: The complete control rates observed after 3, 6 and 12 months were respectively: 6.9%, 10.3% and 3.4%, while the response rates were accordingly 44.8%, 58.6% and 39.6%. The ameliorative rate of EGG reached 65.5%, appearing in positive correlation with the clinical efficacy (r = 0.436, p = 0.001). The retention rate after one year was 89%. Adverse reactions were expressed in 3% of the child patients, and the symptoms were dysphoria, mental and behavior disorders. CONCLUSIONS: The levetiracetam add-on therapy for child refractory epilepsy, demonstrates fast and obvious efficacy as well as fewer adverse reactions.
机译:目的:探讨左乙拉西坦(LEV)联合治疗儿童难治性癫痫的临床疗效和安全性。患者和方法:对65例难治性癫痫和临床发作的儿童进行了左乙拉西坦附加疗法的测试。在治疗后的三个月,六个月和十二个月中,分别观察到这些儿童的脑电图(EGG)变化和不良反应。结果:3、6和12个月后观察到的完全控制率分别为:6.9%,10.3%和3.4%,相应的缓解率分别为44.8%,58.6%和39.6%。 EGG的改善率达到65.5%,与临床疗效呈正相关(r = 0.436,p = 0.001)。一年后的保留率为89%。 3%的儿童患者出现不良反应,症状为烦躁不安,精神和行为障碍。结论:左乙拉西坦治疗儿童难治性癫痫的附加疗法显示出快速而明显的疗效以及较少的不良反应。

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