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对有注意力缺陷多动障碍症状儿童的长期兴奋剂治疗。一项随机、双盲、安慰剂对照试验。

Long-term stimulant treatment of children with attention-deficit hyperactivity disorder symptoms. A randomized, double-blind, placebo-controlled trial.

作者信息

Gillberg C, Melander H, von Knorring A L, Janols L O, Thernlund G, Hägglöf B, Eidevall-Wallin L, Gustafsson P, Kopp S

机构信息

Department of Child and Adolescent Psychiatry, University of Göteborg, Sweden.

出版信息

Arch Gen Psychiatry. 1997 Sep;54(9):857-64. doi: 10.1001/archpsyc.1997.01830210105014.

Abstract

BACKGROUND

We wanted to study the effects of amphetamine on symptoms of attention-deficit hyperactivity disorder (ADHD) over a longer period than has been reported in previous studies of central stimulants in this condition.

METHODS

Sixty-two children, aged 6 to 11 years, meeting DSM-III-R symptom criteria for ADHD participated in a parallel-group design, randomized, double-blind, placebo-controlled study of amphetamine treatment. Treatment was not restricted to children with "pure" ADHD, ie, some had comorbid diagnoses. In the amphetamine group, children received active treatment for 15 months.

RESULTS

Amphetamine was clearly superior to placebo in reducing inattention, hyperactivity, and other disruptive behavior problems and tended to lead to improved results on the Wechsler Intelligence Scale for Children--Revised. Treatment failure rate was considerably lower and time to treatment failure was longer in the amphetamine group. Adverse effects were few and relatively mild.

CONCLUSION

The results of this long-term, placebo-controlled study of the central stimulant amphetamine in the treatment of ADHD indicate that there are remaining positive effects of the drug 15 months after starting treatment.

摘要

背景

我们希望研究苯丙胺对注意力缺陷多动障碍(ADHD)症状的影响,研究时长要超过此前关于中枢兴奋剂治疗该疾病的研究报告。

方法

62名年龄在6至11岁、符合DSM-III-R ADHD症状标准的儿童参与了一项平行组设计、随机、双盲、安慰剂对照的苯丙胺治疗研究。治疗对象不限于“单纯”ADHD儿童,即部分儿童有共病诊断。在苯丙胺组,儿童接受了15个月的积极治疗。

结果

在减少注意力不集中、多动及其他破坏性行为问题方面,苯丙胺明显优于安慰剂,并且在韦氏儿童智力量表修订版上的成绩往往更好。苯丙胺组的治疗失败率明显更低,治疗失败时间更长。不良反应少且相对较轻。

结论

这项关于中枢兴奋剂苯丙胺治疗ADHD的长期、安慰剂对照研究结果表明,开始治疗15个月后,该药物仍有积极效果。

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