Alejandro G Szmulewicz, Hanna Gerlovin, Nick Rezaee, William Robb, Gonzalo Martínez-Alés, Howard Liu, Robert M Bossarte, Eric G Smith, Ira Katz, Ryan Ferguson, Ronald C Kessler, Miguel A Hernan
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引用次数: 0
Abstract
Background: Lithium has long been considered to reduce suicidal behaviour in patients with affective disorders, but evidence from large real-world populations remains limited.
Objective: To estimate the effects of lithium initiation and continuation on suicide deaths and non-lethal suicidal behaviours among adults with bipolar disorder or major depressive disorder.
Methods: We emulated two target trials using electronic health records and administrative claims from US veterans between January 2010 and December 2022. The first trial benchmarked results against the CSP-590 randomised trial by estimating the 1-year risk of suicide-related events (non-fatal suicide attempts, hospitalisations to prevent suicide or suicide deaths) among patients with a recent suicide attempt initiating lithium versus not initiating lithium. The second trial extended follow-up to 10 years to estimate risks of suicide deaths and non-lethal suicidal behaviours separately, including subgroup analyses by age and diagnosis. An additional analysis removed the requirement of a prior suicide attempt.
Findings: In the benchmarking analysis, the 1-year risk ratio for suicide-related events comparing lithium initiation with no initiation was 1.06 (95% CI 1.01 to 1.12), consistent with findings from the CSP-590 trial. In the extended analysis, the 10-year per-protocol risk ratio for suicide death was 1.00 (95% CI 0.86 to 1.15) and for non-lethal suicidal behaviours was 0.96 (95% CI 0.90 to 1.02). Results were similar among individuals with and without a prior suicide attempt.
Conclusion: When added to ongoing pharmacological treatment for patients with affective disorders, lithium may not substantially reduce suicide risk highlighting the need for additional suicide prevention strategies in this population. Limitations include lack of information on adherence, dosage or blood levels of lithium which may have obscured existing differences.
Clinical implications: Our findings suggest that adding lithium therapy to the ongoing treatment regimens of patients with affective disorders for the sole purpose of reducing suicide may not be well-tolerated or meaningfully reduce suicide risk.
背景:长期以来,锂一直被认为可以减少情感性障碍患者的自杀行为,但来自现实世界大量人群的证据仍然有限。目的:评估锂盐起始和持续治疗对双相情感障碍或重度抑郁症成人自杀死亡和非致命性自杀行为的影响。方法:我们利用2010年1月至2022年12月期间美国退伍军人的电子健康记录和行政索赔,模拟了两项目标试验。第一项试验以CSP-590随机试验的结果为基准,通过估计最近有自杀企图的患者在1年内发生自杀相关事件(非致命性自杀企图、住院预防自杀或自杀死亡)的风险,开始服用锂与未开始服用锂。第二项试验将随访时间延长至10年,分别评估自杀死亡和非致命性自杀行为的风险,包括按年龄和诊断进行亚组分析。另一项分析取消了先前自杀企图的要求。结果:在基准分析中,比较锂起始治疗与未起始治疗的自杀相关事件的1年风险比为1.06 (95% CI 1.01 - 1.12),与CSP-590试验的结果一致。在扩展分析中,自杀死亡的10年每方案风险比为1.00 (95% CI 0.86至1.15),非致命性自杀行为的10年每方案风险比为0.96 (95% CI 0.90至1.02)。在有和没有自杀企图的个体中,结果相似。结论:当添加到情感性障碍患者的持续药物治疗中时,锂可能不会显著降低自杀风险,这突出了在这一人群中需要额外的自杀预防策略。局限性包括缺乏关于锂的依从性、剂量或血液水平的信息,这可能掩盖了现有的差异。临床意义:我们的研究结果表明,在情感性障碍患者的持续治疗方案中加入锂治疗,以减少自杀的唯一目的可能无法很好地耐受或有意义地降低自杀风险。