Fergusson Dean, Doucette Steve, Glass Kathleen Cranley, Shapiro Stan, Healy David, Hebert Paul, Hutton Brian
Ottawa Health Research Institute, Clinical Epidemiology Program, 501 Smyth Road, Box 201, Ottawa, Ontario, Canada K1H 8L6.
BMJ. 2005 Feb 19;330(7488):396. doi: 10.1136/bmj.330.7488.396.
To establish whether an association exists between use of selective serotonin reuptake inhibitors (SSRIs) and suicide attempts.
Systematic review of randomised controlled trials.
Medline and the Cochrane Collaboration's register of controlled trials (November 2004) for trials produced by the Cochrane depression, anxiety, and neurosis group.
Studies had to be randomised controlled trials comparing an SSRI with either placebo or an active non-SSRI control. We included clinical trials that evaluated SSRIs for any clinical condition. We excluded abstracts, crossover trials, and all trials whose follow up was less than one week.
Seven hundred and two trials met our inclusion criteria. A significant increase in the odds of suicide attempts (odds ratio 2.28, 95% confidence 1.14 to 4.55, number needed to treat to harm 684) was observed for patients receiving SSRIs compared with placebo. An increase in the odds ratio of suicide attempts was also observed in comparing SSRIs with therapeutic interventions other than tricyclic antidepressants (1.94, 1.06 to 3.57, 239). In the pooled analysis of SSRIs versus tricyclic antidepressants, we did not detect a difference in the odds ratio of suicide attempts (0.88, 0.54 to 1.42).
Our systematic review, which included a total of 87 650 patients, documented an association between suicide attempts and the use of SSRIs. We also observed several major methodological limitations in the published trials. A more accurate estimation of risks of suicide could be garnered from investigators fully disclosing all events.
确定选择性5-羟色胺再摄取抑制剂(SSRI)的使用与自杀未遂之间是否存在关联。
对随机对照试验进行系统评价。
Medline以及Cochrane协作网的对照试验注册库(2004年11月),以获取Cochrane抑郁、焦虑和神经症小组开展的试验。
研究必须为将一种SSRI与安慰剂或活性非SSRI对照进行比较的随机对照试验。我们纳入了评估SSRI用于任何临床状况的临床试验。我们排除了摘要、交叉试验以及所有随访时间少于一周的试验。
702项试验符合我们的纳入标准。与安慰剂相比,接受SSRI治疗的患者自杀未遂几率显著增加(优势比2.28,95%置信区间1.14至4.55,伤害需治人数684)。在将SSRI与三环类抗抑郁药以外的治疗干预措施进行比较时,也观察到自杀未遂优势比增加(1.94,1.06至3.57,239)。在SSRI与三环类抗抑郁药的汇总分析中,我们未检测到自杀未遂优势比存在差异(0.88,0.54至1.42)。
我们的系统评价共纳入87650例患者,记录了自杀未遂与SSRI使用之间的关联。我们还观察到已发表试验存在若干主要方法学局限性。研究者充分披露所有事件可能会得出更准确的自杀风险估计。