Campbell M, Anderson L T, Small A M, Adams P, Gonzalez N M, Ernst M
Department of Psychiatry, New York University Medical Center, NY 10016.
J Am Acad Child Adolesc Psychiatry. 1993 Nov;32(6):1283-91. doi: 10.1097/00004583-199311000-00024.
To assess critically the short-term efficacy and safety of naltrexone in autistic children and its effects on discrimination learning in the laboratory.
A parallel group design was employed. After a 2-week placebo baseline period, children were randomly assigned either to naltrexone or to placebo for a period of 3 weeks followed by a one-week posttreatment placebo period. Multiple raters and rating scales were employed in a variety of conditions. Forty-one children, all inpatients, ages 2.9 to 7.8 years, completed the study. Naltrexone reduced hyperactivity and had no effect on discrimination learning in the laboratory. There was a suggestion that it had a beneficial effect on decreasing self-injurious behavior. Untoward effects were mild and transient.
In the present study, naltrexone significantly reduced only hyperactivity, and no serious untoward effects were observed. The effectiveness of naltrexone in the treatment of autism and self-injurious behavior requires additional assessment in a sample of children with moderate to severe self-injurious behavior.
严格评估纳曲酮对自闭症儿童的短期疗效和安全性及其在实验室中对辨别学习的影响。
采用平行组设计。在为期2周的安慰剂基线期后,儿童被随机分配接受纳曲酮或安慰剂治疗3周,随后是为期1周的治疗后安慰剂期。在各种情况下使用了多个评估者和评定量表。41名年龄在2.9至7.8岁的住院儿童完成了该研究。纳曲酮减少了多动,且对实验室中的辨别学习没有影响。有迹象表明它对减少自伤行为有有益作用。不良反应轻微且短暂。
在本研究中,纳曲酮仅显著降低了多动,未观察到严重不良反应。纳曲酮在治疗自闭症和自伤行为方面的有效性需要在中度至重度自伤行为儿童样本中进行额外评估。