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[艾司西酞普兰的疗效与抑郁严重程度:新数据]

[Efficacy of escitalopram and severity of depression: new data].

作者信息

Spadone C

机构信息

CHU Saint-Louis, AP-HP, université Paris-Diderot, 1, avenue Claude-Vellefaux, 75010 Paris, France.

出版信息

Encephale. 2009 Dec;35(6):577-85. doi: 10.1016/j.encep.2009.10.004.

Abstract

According to recent data in the literature, severe forms of depression represent almost half of all characterised episodes of depression; in view of this their treatment is a real public health challenge. According to the recommendations of various health authorities, treatment first relies on antidepressant medication. A recent meta-analysis of 12 new generation antidepressants has shown that these products are not all equivalent in the treatment of major depression, and that differences exist in terms not only of efficacy but also of acceptability. These differences in efficacy also appear true in the treatment of severe depression. Very recent publications, with a meta-analysis carried out on large cohorts of patients included in clinical trials, have shown the superior efficacy of escitalopram (which is the most active enantiomer of the racemic component, citalopram) in severe depression (defined by a total score on the MADRS scale > or =30). A pooled analysis by Kilts et al. assessed the response to treatment according to the baseline severity of the depression, under escitalopram and under six comparable products: citalopram, duloxetine, fluoxetine, paroxetine, sertraline, and venlafaxine. It showed that the rate of responders to the different treatments decreased when baseline severity increased, which agrees with the data in the literature, except for escitalopram, with which the rate of responders remained stable. The pooled analysis of Kennedy et al., that partly referred to the same studies, showed that for all the patients exhibiting severe depression, escitalopram was significantly superior to the other same six comparable products (mean estimated difference of 1.8 on the total MADRS score [p<0.0001]; a rate of 64.4 responders vs 55.8% [odds ratio=1.60, p<0.0001]; rate of remission of 47.7 vs 41.6% [odds ratio=1.39, p<0.0007]). In parallel with the statistical significance of the results, the criterion of clinical pertinence of the differences revealed between the medicinal products is highly significant. Regarding antidepressants, the criteria of clinical pertinence most frequently applied are the difference in rate of responders, the number needed to treat (NNT) and, to a lesser extent, the difference between the rates of patients in remission and the difference in the effect of treatment. According to these criteria, Montgomery and Möller (2009) assessed the clinical pertinence of the results showing the superior efficacy of escitalopram on three products: citalopram, paroxetine and duloxetine. Hence, they established this clinical pertinence for all of the depressed patients, but also in the particular case of severe depression. All these new data confirm the interest of escitalopram in the treatment of characterised depression and notably in the severe forms, with a particularly favourable efficacy/acceptability ratio.

摘要

根据文献中的最新数据,重度抑郁症几乎占所有已确诊抑郁症发作病例的一半;鉴于此,其治疗成为一项切实的公共卫生挑战。根据各卫生当局的建议,治疗首先依赖抗抑郁药物。最近一项对12种新一代抗抑郁药的荟萃分析表明,这些产品在治疗重度抑郁症方面并非都等效,不仅在疗效方面存在差异,在可接受性方面也有不同。这些疗效差异在重度抑郁症治疗中似乎也很明显。最近的出版物,通过对纳入临床试验的大量患者队列进行荟萃分析,已显示艾司西酞普兰(其是消旋体西酞普兰中最具活性的对映体)在重度抑郁症(定义为蒙哥马利抑郁评定量表总分≥30分)治疗中疗效更佳。Kilts等人的一项汇总分析根据抑郁症的基线严重程度评估了艾司西酞普兰以及六种可比产品(西酞普兰、度洛西汀、氟西汀、帕罗西汀、舍曲林和文拉法辛)的治疗反应。结果显示,随着基线严重程度增加,不同治疗的反应者比例下降,这与文献数据相符,但艾司西酞普兰除外,其反应者比例保持稳定。Kennedy等人的汇总分析部分参考了相同的研究,结果显示,对于所有患有重度抑郁症的患者,艾司西酞普兰显著优于其他六种可比产品(蒙哥马利抑郁评定量表总分的平均估计差异为1.8 [p<0.0001];反应者比例为64.4% 对55.8% [优势比=1.60,p<0.0001];缓解率为47.7% 对41.6% [优势比=1.39,p<0.0007])。与结果的统计学显著性并行的是,所揭示的药品之间差异的临床相关性标准具有高度显著性。对于抗抑郁药,最常应用的临床相关性标准是反应者比例差异、需治疗人数(NNT),以及在较小程度上,缓解患者比例差异和治疗效果差异。根据这些标准,Montgomery和Möller(2009年)评估了显示艾司西酞普兰对三种产品(西酞普兰、帕罗西汀和度洛西汀)疗效更佳的结果的临床相关性。因此,他们确定了这一临床相关性不仅适用于所有抑郁症患者,也适用于重度抑郁症的特殊情况。所有这些新数据证实了艾司西酞普兰在治疗已确诊抑郁症尤其是重度抑郁症方面的价值,其疗效/可接受性比特别有利。

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