Moncrieff Joanna, Kirsch Irving
University College London, Division of Psychiatry, Maple House, 149, Tottenham Court Road, London, W1T 7NF, UK.
Harvard Medical School, Program in Placebo Studies, Beth Israel Deaconess Medical Centre, 330 Brookline Avenue, Boston, MA 02215, United States.
Contemp Clin Trials. 2015 Jul;43:60-2. doi: 10.1016/j.cct.2015.05.005. Epub 2015 May 12.
Meta-analyses indicate that antidepressants are superior to placebos in statistical terms, but the clinical relevance of the differences has not been established. Previous suggestions of clinically relevant effect sizes have not been supported by empirical evidence. In the current paper we apply an empirical method that consists of comparing scores obtained on the Hamilton rating scale for depression (HAM-D) and scores from the Clinical Global Impressions-Improvement (CGI-I) scale. This method reveals that a HAM-D difference of 3 points is undetectable by clinicians using the CGI-I scale. A difference of 7 points on the HAM-D, or an effect size of 0.875, is required to correspond to a rating of 'minimal improvement' on the CGI-I. By these criteria differences between antidepressants and placebo in randomised controlled trials, including trials conducted with people diagnosed with very severe depression, are not detectable by clinicians and fall far short of levels consistent with clinically observable minimal levels of improvement. Clinical significance should be considered alongside statistical significance when making decisions about the approval and use of medications like antidepressants.
荟萃分析表明,从统计学角度来看,抗抑郁药优于安慰剂,但差异的临床相关性尚未得到证实。先前有关具有临床相关性效应大小的建议并未得到实证证据的支持。在本文中,我们采用了一种实证方法,即比较汉密尔顿抑郁量表(HAM-D)得分与临床总体印象改善量表(CGI-I)得分。该方法表明,使用CGI-I量表的临床医生无法检测到HAM-D有3分的差异。HAM-D相差7分,即效应大小为0.875,才相当于CGI-I量表上的“轻度改善”评级。根据这些标准,临床医生无法检测到随机对照试验中抗抑郁药与安慰剂之间的差异,包括对被诊断为非常严重抑郁症的患者进行的试验,且这些差异远低于与临床上可观察到的最小改善水平相一致的程度。在决定批准和使用抗抑郁药等药物时,应将临床意义与统计学意义一并考虑。