文拉法辛治疗重度抑郁症成人患者的不良事件风险:随机临床试验的系统回顾、荟萃分析和试验序列分析。

IF 5.9 2区 医学 Q1 PSYCHIATRY
C B Kamp, J J Petersen, P Faltermeier, S Juul, F Siddiqui, J Moncrieff, M A Horowitz, M P Hengartner, I Kirsch, C Gluud, J C Jakobsen
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引用次数: 0

摘要

目的:文拉法辛在全球范围内被用于治疗抑郁症。以往的综述表明,文拉法辛能降低抑郁评分量表的得分,其结果具有统计学意义,但与患者的相关性仍不确定。关于文拉法辛相关不良反应的发生率,以前一直是基于非随机研究的结果。我们的主要目的是评估文拉法辛在随机试验中治疗成人重度抑郁症患者时发生不良反应的风险:我们检索了从开始到 2024 年 3 月 7 日的相关数据库和其他来源,以了解在成人重度抑郁障碍患者中比较文拉法辛与安慰剂或无干预措施的随机临床试验。采用荟萃分析法和试验序列分析法对数据进行了综合。主要结果为自杀或自杀未遂、严重不良事件和非严重不良事件:我们纳入了28项试验,将6253名参与者随机分为文拉法辛与安慰剂两组。所有结果的偏倚风险都很高,证据的确定性很低。所有试验均在随机化后最长12周进行了结果评估。元分析和试验序列分析显示,没有足够的信息来评估文拉法辛对自杀或自杀未遂风险的影响。Meta分析显示,有证据表明文拉法辛与安慰剂相比会对严重不良事件造成危害(风险比:2.66;95%置信区间:1.67-4.25;P < 0.01;22项试验),主要是由于性功能障碍和厌食症的风险较高。Meta分析表明,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、气喘、震颤和食欲下降:短期结果显示,文拉法辛对自杀风险的影响不确定,但会增加严重不良事件(尤其是性功能障碍和厌食症)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,鉴于许多人使用文拉法辛长达数年之久,目前尚无关于文拉法辛长期不良反应的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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; p < 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.

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来源期刊
CiteScore
7.80
自引率
1.20%
发文量
121
审稿时长
>12 weeks
期刊介绍: Epidemiology and Psychiatric Sciences is a prestigious international, peer-reviewed journal that has been publishing in Open Access format since 2020. Formerly known as Epidemiologia e Psichiatria Sociale and established in 1992 by Michele Tansella, the journal prioritizes highly relevant and innovative research articles and systematic reviews in the areas of public mental health and policy, mental health services and system research, as well as epidemiological and social psychiatry. Join us in advancing knowledge and understanding in these critical fields.
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