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Is Escitalopram Really Relevantly Superior to Citalopram in Treatment of Major Depressive Disorder? A Meta-analysis of Head-tohead Randomized Trials

机译:在严重抑郁症的治疗中,依西酞普兰真的比西酞普兰更重要吗?头对头随机试验的荟萃分析

摘要

Aim To evaluate clinical relevance of differences betweenescitalopram and citalopram (equimolar) for major depressivedisorder.Methods Review and meta-analysis of comparative randomizedcontrolled trials (RCT). Comparisons were in relationto Montgomery-Asberg depression rating scale(MADRS) score reduction at weeks 1 (5 RCTs), 4 (5 RCTs), 6(4 RCTs), 8 (5 RCTs), and 24 (1 RCT); proportion of respondersat weeks 2, 4, 6 (2 RCTs for each time point), 8 (5 RCTs),and 24 (1 RCT); clinical global impression-severity (CGI-S)reduction at weeks 6 (1 RCT), 8 (5 RCTs), and 24 (1 RCT),and discontinuation due to adverse events or inefficacyduring short-term (up to 8 weeks) and medium-term (24weeks) treatment.Results MADRS reduction was greater with escitalopram,but 95% confidence intervals (CI) around the mean differencewere entirely or largely below 2 scale points (minimallyimportant difference) and CI around the effect size(ES) was below 0.32 (“small”) at all time points. Risk of responsewas higher with escitalopram at week 8 (relativerisk, 1.14; 95% CI, 1.04 to 1.26) but number needed to treatwas 14 (95% CI, 7 to 111). All 95% CIs around the mean differenceand ES of CGI-S reduction at week 8 were below0.32 points and the limit of “small,” respectively. Data for severepatients (MADRS≥30) are scarce (only 1 RCT), indicatingsomewhat greater efficacy (response rate and MADRSreduction at week 8, but not CGI-S reduction) of escitalopram,but without compelling evidence of clinically relevantdifferences. Discontinuations due to adverse eventsor inefficacy up to 8 weeks of treatment were comparable.Data for the period up to 24 weeks are scarce and inconclusive.Conclusion Presently, the claims about clinically relevantsuperiority of escitalopram over citalopram in short-to-mediumterm treatment of major depressive disorder are notsupported by evidence.
机译:目的评价依西酞普兰和西酞普兰(等摩尔)之间的差异对主要抑郁症的临床意义。方法回顾性比较对照研究(RCT)和荟萃分析。比较在第1周(5 RCT),4(5 RCT),6(4 RCT),8(5 RCT)和24(1 RCT)时的蒙哥马利-阿斯伯格抑郁量表(MADRS)得分降低;第2、4、6周(每个时间点2个RCT),8个(5 RCT)和24个(1 RCT)响应者的比例;在第6周(1 RCT),8周(5 RCT)和24周(1 RCT)时临床总体印象严重度(CGI-S)降低,以及由于不良事件或短期(至多8周)无效而终止治疗结果:依他普仑治疗可使MADRS降低更大,但平均差异周围的95%置信区间(CI)完全或大大低于2个标度点(最小重要差异),且效应量(ES)周围的CI低于在所有时间点均为0.32(“小”)。依他普仑在第8周的反应风险较高(相对风险为1.14; 95%CI为1.04至1.26),但需要治疗的人数为14(95%CI为7至111)。在第8周,平均差和CGI-S降低的ES周围的所有95%CI均低于0.32点和“小”限值。重症患者(MADRS≥30)的数据稀少(仅1个RCT),表明依他普仑的疗效(在第8周时缓解率和MADRS降低,但CGI-S降低不明显),但无明显的临床相关差异证据。在8周的治疗中因不良事件或无效而停药的情况是可比的。长达24周的数据尚无定论。没有证据支持这种疾病。

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    Trkulja Vladimir;

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  • 年度 2010
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