Pandina Gahan J, Bossie Cynthia A, Youssef Eriene, Zhu Young, Dunbar Fiona
Medical Affairs, Janssen Pharmaceutica, Inc., Titusville, NJ 08560, USA.
J Autism Dev Disord. 2007 Feb;37(2):367-73. doi: 10.1007/s10803-006-0234-7.
Subgroup analysis of children (5-12 years) with autism enrolled in an 8-week, double-blind, placebo-controlled trial of risperidone for pervasive developmental disorders. The primary efficacy measure was the Aberrant Behavior Checklist-Irritability (ABC-I) subscale. Data were available for 55 children given risperidone (n=27) or placebo (n=28); mean baseline ABC-I ( +/- SD) was 20.6 (8.1) and 21.6 (10.2). Risperidone [mean dose ( +/- SD): 1.37 mg/day (0.7)] resulted in significantly greater reduction from baseline to endpoint in ABC-I versus placebo [mean change ( +/- SD): -13.4 (1.5) vs. -7.2 (1.4), P<0.05; ES=-0.7]. The most common adverse effect with risperidone was somnolence (74% vs. 7% with placebo). Risperidone treatment was well tolerated and significantly improved behavioral problems associated with autism.
对参加为期8周的利培酮治疗广泛性发育障碍双盲、安慰剂对照试验的5至12岁自闭症儿童进行亚组分析。主要疗效指标为异常行为检查表-易激惹(ABC-I)子量表。有55名接受利培酮(n=27)或安慰剂(n=28)治疗的儿童的数据;ABC-I的平均基线值(±标准差)为20.6(8.1)和21.6(10.2)。与安慰剂相比,利培酮[平均剂量(±标准差):1.37毫克/天(0.7)]从基线到终点时ABC-I的降低幅度显著更大[平均变化(±标准差):-13.4(1.5)对-7.2(1.4),P<0.05;效应量=-0.7]。利培酮最常见的不良反应是嗜睡(74%,而安慰剂组为7%)。利培酮治疗耐受性良好,显著改善了与自闭症相关的行为问题。