From the Department of Clinical Neuroscience, Karolinska Institutet, Stockholm; the Department of Forensic Psychiatry, University of Eastern Finland, Niuvanniemi Hospital, Kuopio; and the Department of Mental Health and Substance Abuse Services, National Institute for Health and Welfare, Helsinki.
Am J Psychiatry. 2016 Jun 1;173(6):600-6. doi: 10.1176/appi.ajp.2015.15050618. Epub 2015 Dec 7.
Although mortality related to psychotropic medications has received much attention in recent years, little is known about the relationship between risk of death and cumulative antipsychotic load, and even less about the relationship between mortality and cumulative exposure to antidepressants or benzodiazepines. The authors examined these relationships using nationwide databases.
The authors used prospectively collected nationwide databases to identify all individuals 16-65 years of age with a schizophrenia diagnosis (N=21,492) in Sweden. All-cause and cause-specific mortality rates were calculated as a function of cumulative low, moderate, and high exposure to antipsychotics, antidepressants, and benzodiazepines from 2006 through 2010.
Compared with no exposure, both moderate (adjusted hazard ratio=0.59, 95% CI=0.49-0.70) and high (adjusted hazard ratio=0.75, 95% CI=0.63-0.89) antipsychotic exposures were associated with substantially lower overall mortality. Moderate antidepressant exposure was associated with a lower mortality (adjusted hazard ratio=0.85, 95% CI=0.73-0.98), and high exposure, even lower (adjusted hazard ratio=0.71, 95% CI=0.59-0.86). Exposure to benzodiazepines showed a dose-response relationship with mortality (hazard ratios up to 1.74 [95% CI=1.50-2.03]).
Moderate and high-dose antipsychotic and antidepressant use were associated with 15%-40% lower overall mortality, whereas chronic high-dose use of benzodiazepines was associated with up to a 70% higher risk of death compared with no exposure. Since patients with anxiety and depressive symptoms may have a higher intrinsic risk of death, the finding for benzodiazepines may be attributable to some extent to residual confounding.
尽管近年来人们对精神药物相关死亡率给予了高度关注,但对于死亡风险与累积抗精神病药剂量之间的关系知之甚少,甚至对于与抗抑郁药或苯二氮䓬类药物的累积暴露相关的死亡率也知之甚少。作者使用全国性数据库研究了这些关系。
作者使用前瞻性收集的全国性数据库,确定了瑞典年龄在 16-65 岁之间的所有精神分裂症患者(n=21492)。计算了从 2006 年到 2010 年期间,低、中、高累积暴露于抗精神病药、抗抑郁药和苯二氮䓬类药物与全因和特定原因死亡率之间的关系。
与无暴露相比,中剂量(调整后的危险比=0.59,95%可信区间=0.49-0.70)和高剂量(调整后的危险比=0.75,95%可信区间=0.63-0.89)抗精神病药物暴露与整体死亡率显著降低相关。中剂量抗抑郁药暴露与死亡率降低相关(调整后的危险比=0.85,95%可信区间=0.73-0.98),而高剂量暴露甚至更低(调整后的危险比=0.71,95%可信区间=0.59-0.86)。苯二氮䓬类药物暴露与死亡率呈剂量反应关系(危险比高达 1.74[95%可信区间 1.50-2.03])。
中剂量和高剂量抗精神病药和抗抑郁药的使用与总死亡率降低 15%-40%相关,而慢性高剂量使用苯二氮䓬类药物与无暴露相比,死亡风险增加高达 70%。由于患有焦虑和抑郁症状的患者可能具有更高的内在死亡风险,因此苯二氮䓬类药物的发现可能在一定程度上归因于残余混杂因素。