Snyder Richard, Turgay Atilla, Aman Michael, Binder Carin, Fisman Sandra, Carroll Allan
Royal University Hospital, Saskatoon, Saskatchewan, Canada.
J Am Acad Child Adolesc Psychiatry. 2002 Sep;41(9):1026-36. doi: 10.1097/00004583-200209000-00002.
To determine whether risperidone is effective in reducing symptoms of disruptive behaviors (such as aggression, impulsivity, defiance of authority figures, and property destruction) associated with conduct disorder, oppositional defiant disorder, and disruptive behavior disorder-not otherwise specified in children with subaverage IQs.
The trial consisted of a 1-week, single-blind, placebo run-in period and was followed by a 6-week, double-blind, placebo-controlled period. One hundred ten children (aged 5-12 years inclusive) with an IQ of 36-84 with a disruptive behavior disorder and a score of at least 24 on the Conduct Problem subscale of the Nisonger Child Behavior Rating Form (NCBRF) were enrolled. Eighty percent of subjects had comorbid attention-deficit/hyperactivity disorder (ADHD). Risperidone doses ranged from 0.02 to 0.06 mg/kg per day. Subjects were rated on the NCBRF, Aberrant Behavior Checklist, Behavior Problems Inventory, Clinical Global Impressions (CGI), modified California Verbal Learning Test (CVLT), and a continuous performance task (CPT).
The intention-to-treat analysis of risperidone-treated subjects showed a significant (p < .001) reduction in mean scores (from 33.4 at baseline to 17.6 at end point; 47.3% reduction) versus placebo-treated subjects (mean baseline of 32.6 to 25.8 at end point; 20.9% reduction) on the Conduct Problem subscale of the NCBRF. Between-group differences in favor of risperidone were seen as early as week 1 and were significant at all post-baseline visits. Other subscales showed significant improvement with risperidone compared with placebo. CGI scale ratings of improvement showed highly significant gains for risperidone over placebo. A subanalysis demonstrated that the effect of risperidone was unaffected by diagnosis, presence/absence of ADHD, psychostimulant use, IQ status, and somnolence. Risperidone produced no changes on the cognitive variables (CPT/modified CVLT). The most common side effects included somnolence, headache, appetite increase, and dyspepsia. Side effects related to extrapyramidal symptoms were reported in 7 (13.2%) and 3 (5.3%) of the subjects in the risperidone and placebo groups, respectively (p = .245).
Risperidone appears to be an adequately tolerated and effective treatment in children with subaverage IQs and severe disruptive behaviors such as aggression and destructive behavior.
确定利培酮对于降低智商低于平均水平的儿童中与品行障碍、对立违抗障碍及未特定的破坏性行为障碍相关的破坏性行为症状(如攻击行为、冲动、违抗权威人物及破坏财物行为)是否有效。
该试验包括为期1周的单盲安慰剂导入期,随后是为期6周的双盲安慰剂对照期。招募了110名年龄在5至12岁(含)、智商为36至84、患有破坏性行为障碍且在尼森格儿童行为评定量表(NCBRF)的品行问题子量表上得分至少为24分的儿童。80%的受试者患有共病注意力缺陷/多动障碍(ADHD)。利培酮剂量范围为每日0.02至0.06毫克/千克。受试者在NCBRF、异常行为检查表、行为问题量表、临床总体印象(CGI)、改良的加利福尼亚言语学习测试(CVLT)及持续性操作任务(CPT)上接受评定。
对接受利培酮治疗的受试者进行的意向性分析显示,与接受安慰剂治疗的受试者相比,在NCBRF的品行问题子量表上,平均得分有显著降低(p <.001)(从基线时的33.4降至终点时的17.6;降低47.3%),而接受安慰剂治疗的受试者从基线时的32.6降至终点时的25.8(降低20.9%)。早在第1周就观察到利培酮组与安慰剂组之间存在有利于利培酮的组间差异,且在基线后的所有访视中均显著。与安慰剂相比,利培酮在其他子量表上也显示出显著改善。CGI改善量表评分显示利培酮比安慰剂有高度显著的改善。一项亚组分析表明,利培酮的效果不受诊断、是否存在ADHD、是否使用精神兴奋剂、智商状态及嗜睡的影响。利培酮对认知变量(CPT/改良CVLT)无影响。最常见的副作用包括嗜睡、头痛、食欲增加及消化不良。利培酮组和安慰剂组分别有7名(13.2%)和3名(5.3%)受试者报告了与锥体外系症状相关的副作用(p =.245)。
对于智商低于平均水平且有攻击和破坏行为等严重破坏性行为的儿童,利培酮似乎是一种耐受性良好且有效的治疗方法。