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首页> 外文期刊>BMC Psychiatry >Vortioxetine in the treatment of adult patients with major depressive disorder: a meta-analysis of randomized double-blind controlled trials
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Vortioxetine in the treatment of adult patients with major depressive disorder: a meta-analysis of randomized double-blind controlled trials

机译:伏替西汀治疗成人重度抑郁症:随机双盲对照试验的荟萃分析

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Background Vortioxetine is a novel multimodal compound that has recently been approved by the FDA for the treatment of major depressive disorder (MDD). It is a selective serotonin (5-HT) 3A and 5-HT7 receptor antagonist, 5-HT1B receptor partial agonist, 5-HT1A receptor agonist and inhibitor of serotonin transporters. The objective of this meta-analysis was to evaluate the efficacy and safety of vortioxetine in adults with MDD. Methods A literature search was conducted in the databases of PubMed, EMBASE, Cochrane library and HINARI. The meta-analysis was conducted by including randomized controlled trials that assessed the efficacy and safety of vortioxetine in adult patients with MDD. Using the random effects model, which assumes individual studies are estimating different treatment effects, the efficacy and safety of vortioxetine was determined by weighted mean differences (WMDs) and odds ratios (ORs). The findings were considered as statistically significant when the 95% CI of WMDs and ORs did not include 0 and 1, respectively. Heterogeneity testing, meta-regression and sensitivity analysis were also performed. Results During the initial literature search about 151 publications were identified. Based on the predetermined inclusion criteria, 7 randomized controlled trials were included. The pooled analysis demonstrated a statistically significant reduction in the Montgomery–?sberg Depression Rating Scale (MADRS) total score from baseline among patients who were on vortioxetine (WMD?=??3.92; 95% CI, ?5.258 to ?2.581). Furthermore, a statistically significant number of patients with MDD who were on vortioxetine have achieved a greater than or equal to 50% reduction in depression symptoms from baseline. However, a significant number of patients who were on vortioxetine therapy reported more adverse events than patients who were on placebo (overall OR?=?1.21; 95% CI, 1.06 to 1.38). Conclusions Therapy with vortioxetine was significantly associated with reduction in depression symptoms from baseline compared to placebo. Nevertheless, a significant number of patients who were on vortioxetine therapy have reported more adverse events.
机译:背景技术Vortioxetine是一种新型的多峰化合物,最近已被FDA批准用于治疗重度抑郁症(MDD)。它是选择性5-羟色胺(5-HT)3A和5-HT7受体拮抗剂,5-HT1B受体部分激动剂,5-HT1A受体激动剂和5-羟色胺转运蛋白抑制剂。这项荟萃分析的目的是评估伏立西汀对MDD成人的疗效和安全性。方法在PubMed,EMBASE,Cochrane库和HINARI的数据库中进行文献检索。荟萃分析是通过纳入随机对照试验进行的,该试验评估了伏替西汀对成年MDD患者的疗效和安全性。使用随机效应模型(该模型假设个别研究正在评估不同的治疗效果),伏立西汀的疗效和安全性由加权均数差(WMD)和优势比(OR)确定。当WMD和OR的95%CI分别不包括0和1时,该发现被认为具有统计学意义。还进行了异质性测试,Meta回归和敏感性分析。结果在最初的文献检索中,共鉴定出约151种出版物。根据预定的纳入标准,纳入了7项随机对照试验。汇总分析显示,在接受伏替西汀治疗的患者中,蒙哥马利?sberg抑郁评分量表(MADRS)总分较基线降低了统计学意义(WMD == 3.92; 95%CI,从5.258降至2.581)。此外,接受伏替西汀治疗的统计学上显着的MDD患者与基线相比,抑郁症状的减轻幅度大于或等于50%。但是,与接受安慰剂治疗的患者相比,接受伏替西汀治疗的患者有更多的不良事件发生(总OR?=?1.21; 95%CI,1.06-1.38)。结论与安慰剂相比,伏替西汀治疗与抑郁症状从基线开始减轻显着相关。尽管如此,仍有大量接受伏替西汀治疗的患者报告了更多的不良事件。

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