Cueva J E, Overall J E, Small A M, Armenteros J L, Perry R, Campbell M
Psychiatry, New York Medical College, Valhalla, NY, USA.
J Am Acad Child Adolesc Psychiatry. 1996 Apr;35(4):480-90. doi: 10.1097/00004583-199604000-00014.
To assess critically the short-term efficacy and safety of carbamazepine in the reduction of aggressiveness in children with diagnosed conduct disorder.
Subjects were children aged 5 to 12 years who were hospitalized for treatment-resistant aggressiveness and explosiveness and who had diagnosed conduct disorder. The study was double-blind and placebo-controlled, using a parallel-groups design. Following a 2-week placebo baseline period, children who met the aggression criteria were randomly assigned to treatments for 6 weeks; the study ended with a 1-week posttreatment placebo period. Multiple raters rated the children independently, using multiple rating scales under four conditions. The main outcome measures included the Overt Aggression Scale, the Global Clinical Judgments (Consensus) Scale, and the Children's Psychiatric Rating Scale.
Twenty-two children, aged 5.33 to 11.7 years, completed the study. Carbamazepine was not superior to placebo at optimal daily doses ranging from 400 to 800 mg, mean 683 mg, at serum levels of 4.98 to 9.1 micrograms/mL. Untoward effects associated with administration of carbamazepine were common.
In this modest sample of children, the superiority of carbamazepine over placebo in reducing aggressive behavior was not demonstrated.
严格评估卡马西平在降低已确诊品行障碍儿童攻击性方面的短期疗效和安全性。
研究对象为5至12岁因难治性攻击性和爆发性而住院且已确诊品行障碍的儿童。该研究采用双盲、安慰剂对照的平行组设计。在为期2周的安慰剂基线期后,符合攻击标准的儿童被随机分配接受为期6周的治疗;研究以1周的治疗后安慰剂期结束。多名评估者在四种情况下使用多个评定量表对儿童进行独立评定。主要结局指标包括公开攻击量表、整体临床判断(共识)量表和儿童精神病评定量表。
22名年龄在5.33至11.7岁之间的儿童完成了研究。在每日最佳剂量为400至800毫克(平均683毫克)、血清水平为4.98至9.1微克/毫升时,卡马西平并不优于安慰剂。与卡马西平给药相关的不良反应很常见。
在这个规模不大的儿童样本中,未证明卡马西平在减少攻击行为方面优于安慰剂。