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文拉法辛治疗成人重性抑郁障碍的不良事件风险:系统评价随机临床试验的Meta 分析和试验序贯分析。

The risks of adverse events with venlafaxine for adults with major depressive disorder: a systematic review of randomised clinical trials with meta-analysis and Trial Sequential Analysis.

机构信息

Copenhagen Trial Unit, Centre for Clinical Intervention Research, The Capital Region, Copenhagen University Hospital - Rigshospitalet, Copenhagen Ø, Denmark.

Department of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark, Odense, Denmark.

出版信息

Epidemiol Psychiatr Sci. 2024 Oct 23;33:e51. doi: 10.1017/S2045796024000520.

Abstract

AIMS

Venlafaxine is used to treat depression worldwide. Previous reviews have demonstrated that venlafaxine lowers scores on depression rating scales, producing statistically significant results but the relevance to patients remains uncertain. Knowledge of the incidence of the adverse effects associated with venlafaxine has previously been based on the results of non-randomised studies. Our primary objective was to assess the risks of adverse events with venlafaxine in the treatment of adults with major depressive disorder in randomised trials.

METHODS

We searched relevant databases and other sources from inception to 7 March 2024 for randomised clinical trials comparing venlafaxine versus placebo or no intervention in adults with major depressive disorder. Data were synthesised using meta-analysis and Trial Sequential Analysis. The primary outcomes were suicides or suicide attempts, serious adverse events and non-serious adverse events.

RESULTS

We included 28 trials randomising 6,253 participants to venlafaxine versus placebo. All results were at high risk of bias, and the certainty of the evidence was very low. All trials assessed outcomes at a maximum of 12 weeks after randomisation. Meta-analysis and Trial Sequential Analysis showed insufficient information to assess the effects of venlafaxine on the risks of suicides or suicide attempts. Meta-analysis showed evidence of harm of venlafaxine versus placebo on serious adverse events (risk ratio: 2.66; 95% confidence interval: 1.67-4.25; < 0.01; 22 trials), mainly due to a higher risk of sexual dysfunction and anorexia. Meta-analysis showed that venlafaxine also increased the risk of several non-serious adverse events: nausea, dry mouth, dizziness, sweating, somnolence, constipation, nervousness, insomnia, asthenia, tremor and decreased appetite.

CONCLUSIONS

Short-term results show that venlafaxine has uncertain effects on the risks of suicides but increases the risks of serious adverse events (especially sexual dysfunction and anorexia) and many non-serious adverse events. The long-term effects of venlafaxine for major depressive disorder are unknown. It is a particular cause for concern that there are no data on the long-term adverse effects of venlafaxine given that so many people use these drugs for several years.

摘要

目的

文拉法辛被广泛用于治疗全球抑郁症患者。此前的综述表明,文拉法辛可降低抑郁评分量表的评分,产生具有统计学意义的结果,但与患者的相关性仍不确定。先前对文拉法辛相关不良反应发生率的了解是基于非随机研究的结果。我们的主要目标是评估文拉法辛治疗成人重度抑郁症的随机试验中不良事件的风险。

方法

我们从成立到 2024 年 3 月 7 日搜索了相关数据库和其他来源,以寻找比较文拉法辛与安慰剂或无干预治疗成人重度抑郁症的随机临床试验。使用荟萃分析和试验序贯分析综合数据。主要结局为自杀或自杀企图、严重不良事件和非严重不良事件。

结果

我们纳入了 28 项随机对照试验,共纳入 6253 名参与者,比较文拉法辛与安慰剂。所有结果均存在高度偏倚风险,证据质量极低。所有试验均在随机分组后 12 周内评估结局。荟萃分析和试验序贯分析显示,信息不足,无法评估文拉法辛对自杀或自杀企图风险的影响。荟萃分析表明,与安慰剂相比,文拉法辛对严重不良事件的危害(风险比:2.66;95%置信区间:1.67-4.25;<0.01;22 项试验),主要是由于性功能障碍和厌食的风险增加。荟萃分析还表明,文拉法辛还增加了几种非严重不良事件的风险:恶心、口干、头晕、出汗、嗜睡、便秘、紧张、失眠、乏力、震颤和食欲下降。

结论

短期结果表明,文拉法辛对自杀风险的影响不确定,但增加了严重不良事件(尤其是性功能障碍和厌食)和许多非严重不良事件的风险。文拉法辛治疗重度抑郁症的长期效果尚不清楚。特别令人担忧的是,没有关于文拉法辛长期不良反应的数据,因为有这么多人使用这些药物多年。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3976/11561525/7cd76ef90a65/S2045796024000520_fig1.jpg

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