Ghanizadeh Ahmad, Sahraeizadeh Aliakbar, Berk Michael
School of Medicine, Research Center for Psychiatry and Behavioral Sciences, Shiraz University of Medical Sciences, School of Medicine, Shiraz, Iran,
Child Psychiatry Hum Dev. 2014;45(2):185-92. doi: 10.1007/s10578-013-0390-x.
Aripiprazole and risperidone are the only FDA approved medications for treating irritability in autistic disorder, however there are no head-to-head data comparing these agents. This is the first prospective randomized clinical trial comparing the safety and efficacy of these two medications in patients with autism spectrum disorders. Fifty nine children and adolescents with autism spectrum disorders were randomized to receive either aripiprazole or risperidone for 2 months. The primary outcome measure was change in Aberrant Behavior Checklist (ABC) scores. Adverse events were assessed. Aripiprazole as well as risperidone lowered ABC scores during 2 months. The rates of adverse effects were not significantly different between the two groups. The safety and efficacy of aripiprazole (mean dose 5.5 mg/day) and risperidone (mean dose 1.12 mg/day) were comparable. The choice between these two medications should be on the basis of clinical equipoise considering the patient's preference and clinical profile.
阿立哌唑和利培酮是美国食品药品监督管理局(FDA)批准的仅有的用于治疗孤独症谱系障碍中易激惹症状的药物,然而,尚无直接比较这两种药物的数据。这是第一项比较这两种药物在孤独症谱系障碍患者中的安全性和有效性的前瞻性随机临床试验。59名患有孤独症谱系障碍的儿童和青少年被随机分配接受阿立哌唑或利培酮治疗2个月。主要结局指标是异常行为检查表(ABC)评分的变化。对不良事件进行了评估。阿立哌唑和利培酮在2个月内均降低了ABC评分。两组之间的不良反应发生率无显著差异。阿立哌唑(平均剂量5.5毫克/天)和利培酮(平均剂量1.12毫克/天)的安全性和有效性相当。在选择这两种药物时,应根据临床权衡,考虑患者的偏好和临床特征。