摘要
目的:探讨奥卡西平口服混悬液单药治疗2岁以下婴幼儿部分性发作癫痫的临床疗效和安全性。方法:收集2岁以下婴幼儿部分性发作癫痫患儿52例,给予奥卡西平口服混悬液单药治疗,起始量为8—10mg/(kg·d),渐加量至20~40mg/(kg·d),随访6~18个月,进行自身对照开放性研究,观察其疗效及安全性。结果:应用奥卡西平口服混悬液治疗后,有效率及控制率分别为94.2%、84.6%,8例(15.4%)患儿发生腹泻、呕吐、纳差、皮疹等不良反应。结论:奥卡西平口服混悬液治疗婴幼儿部分性发作癫痫疗效显著,临床应用方便,安全性好,不良反应较少,值得临床推广应用。
Objective: To evaluate the efficacy and security of children under two years of age with epilepsy partial seizures treated by oxcarbazepine oral suspension monotherapy. Methods : Fifty-two cases of children under two years of age with epilepsy partial seizures were collected. Starting dose of oxcarbazepine was from 8 - 10 mg/( kg . d), and added to 20 - 40 mg/( kg . d) gradually. All patients were followed up for 6 - 18 months in the self-controlled open-label study. The efficacy and safety were evaluated. Results: After taking oxcarbazepine oral suspension monotherapy, effective rate and control rate were 94.2% and 84.6% respectively; and adverse reactions rate was 15.4%. Adverse reactions included diarrhea, vomiting, poor appetite, and skin rash. Conclusions: Oxcarbazepine oral suspension monotherapy has significant effect in children under two years of age with epilepsy partial seizures. It is easy to use, with high-performance security, and few adverse reactions.
出处
《儿科药学杂志》
CAS
2014年第3期13-15,共3页
Journal of Pediatric Pharmacy
关键词
奥卡西平口服混悬液
癫痫
安全性
Oxcarbazepine oral suspension
Epilepsy
Efficacy
Security