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蒙哥马利-阿斯伯格抑郁评定量表、汉密尔顿抑郁评定量表及临床总体印象量表在抗抑郁药物临床试验中的相对敏感性

Relative sensitivity of the Montgomery-Asberg Depression Rating Scale, the Hamilton Depression rating scale and the Clinical Global Impressions rating scale in antidepressant clinical trials.

作者信息

Khan A, Khan S R, Shankles E B, Polissar N L

机构信息

Northwest Clinical Research Center, Bellevue, WA 98004, USA.

出版信息

Int Clin Psychopharmacol. 2002 Nov;17(6):281-5. doi: 10.1097/00004850-200211000-00003.

Abstract

Although early antidepressant clinical trials simply relied on a clinician's judgment as to whether a depressed patient clinically improved or not, the Hamilton Depression (HAM-D) rating scale has become the 'gold standard' to assess the efficacy of new antidepressants. The alternative Montgomery-Asberg Depression Rating Scale (MADRS) has not achieved general acceptance. However, its ease of use warrants evaluation as to whether it is comparable to HAM-D in its sensitivity in detecting antidepressant-placebo differences in antidepressant clinical trials. A retrospective chart review was performed on the records of 208 depressed adult patients that participated in eight randomized, placebo-controlled, double-blind antidepressant clinical trials at the Northwest Clinical Research Center between 1996 and 2000. We compared the effect sizes of the HAM-D, MADRS and Clinical Impressions Rating Scale (CGI-S for severity and CGI-I for improvement) for patients assigned to placebo or an established antidepressant. The effect size (measured as the mean change in rating with antidepressants minus the mean change for placebo divided by the pooled SD of change, adjusted for age, gender and initial scores) was 0.49 with MADRS, 0.53 with HAM-D, 0.55 with CGI-S and 0.59 with CGI-I. The four rating scales had similar effect sizes regardless of the type of antidepressant evaluated. These data suggest that MADRS is as sensitive an instrument as HAM-D for detecting antidepressant efficacy in clinical trials. Thus, MADRS may be a desirable tool in large-scale, pivotal antidepressant clinical trials.

摘要

尽管早期的抗抑郁药物临床试验仅仅依靠临床医生对抑郁患者是否在临床上有所改善的判断,但汉密尔顿抑郁量表(HAM-D)已成为评估新型抗抑郁药物疗效的“金标准”。替代的蒙哥马利-阿斯伯格抑郁评定量表(MADRS)尚未得到广泛认可。然而,其使用的简便性值得评估,以确定在抗抑郁药物临床试验中,它在检测抗抑郁药物与安慰剂差异方面的敏感性是否与HAM-D相当。对1996年至2000年期间在西北临床研究中心参与八项随机、安慰剂对照、双盲抗抑郁药物临床试验的208名成年抑郁患者的记录进行了回顾性图表审查。我们比较了接受安慰剂或已确立的抗抑郁药物治疗的患者在HAM-D、MADRS和临床印象评定量表(CGI-S用于严重程度,CGI-I用于改善情况)上的效应大小。效应大小(计算方法为:抗抑郁药物治疗组评分的平均变化减去安慰剂组评分的平均变化,再除以合并的变化标准差,并根据年龄、性别和初始评分进行调整),MADRS为0.49,HAM-D为0.53,CGI-S为0.55,CGI-I为0.59。无论评估的抗抑郁药物类型如何,这四种评定量表的效应大小相似。这些数据表明,在临床试验中检测抗抑郁药物疗效方面,MADRS与HAM-D一样敏感。因此,MADRS可能是大规模、关键的抗抑郁药物临床试验中一种理想的工具。

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