School of Pharmacy, Sungkyunkwan University, 2066 Seobu-ro, Jangan-gu, Suwon, Gyeong gi-do, South Korea.
Department of Medicine and Program in Public Heath, University of California, Irvine, CA, USA.
Soc Psychiatry Psychiatr Epidemiol. 2019 Dec;54(12):1535-1544. doi: 10.1007/s00127-019-01713-x. Epub 2019 Apr 29.
To evaluate whether the concurrent use of benzodiazepines, antidepressants, and opioid analgesics with zolpidem increases the risk of suicide or triggers suicide compared with the use of zolpidem alone.
We conducted a case-control and case-crossover study using the Korean National Health Insurance Service-National Sample Cohort database. Cases were older than 20 years with a suicide record (International Codes of Disease 10th Revision codes: X-60-X84 and Y87.0 intentional self-harm) between January 1, 2004, and December 31, 2013. For case-control design, ten controls were matched to each case by age, sex, index year, region, income, and health insurance type. For case-crossover analysis, we set hazard period to 60 days and assigned five corresponding sets of control periods of equal length. Exposure was assessed during 60 days before suicide for combinations of benzodiazepines, antidepressants, opioid analgesics with zolpidem against zolpidem alone. We conducted a conditional logistic regression to estimate odds ratios (ORs) and their 95% confidence intervals (CIs).
In the case-control study, the risk of suicide was 2.80-fold higher in cases taking benzodiazepines and antidepressants with zolpidem than in those taking zolpidem alone (adjusted OR [aOR], 2.80; 95% CI, 1.38-5.70). However, in the case-crossover study, suicide risk showed no significant difference (crude OR [cOR], 0.92; 95% CI, 0.55-1.52) and was underpowered.
The results of the traditional case-control study confirmed that the concurrent use of benzodiazepines and antidepressants with zolpidem was associated with an increased risk of suicide compared with the use of zolpidem alone. However, there was no significant difference in the magnitude of risk in the within-person comparison design.
评估与单独使用唑吡坦相比,同时使用苯二氮䓬类药物、抗抑郁药和阿片类镇痛药与唑吡坦合用是否会增加自杀风险或引发自杀。
我们使用韩国国家健康保险服务-国家样本队列数据库进行了病例对照和病例交叉研究。病例为年龄大于 20 岁且有自杀记录(国际疾病分类第 10 次修订版代码:X-60-X84 和 Y87.0 故意自伤)的患者,记录时间为 2004 年 1 月 1 日至 2013 年 12 月 31 日。对于病例对照设计,我们通过年龄、性别、索引年、地区、收入和医疗保险类型,为每个病例匹配了 10 个对照。对于病例交叉分析,我们将危险期设定为 60 天,并为每个病例分配了 5 个长度相等的相应对照期。暴露情况在自杀前 60 天内进行评估,评估内容为同时使用苯二氮䓬类药物、抗抑郁药和阿片类镇痛药与唑吡坦以及单独使用唑吡坦的情况。我们进行了条件逻辑回归分析,以估计比值比(ORs)及其 95%置信区间(CIs)。
在病例对照研究中,与单独使用唑吡坦相比,同时使用苯二氮䓬类药物和抗抑郁药的患者自杀风险高 2.80 倍(调整后的 OR [aOR],2.80;95%CI,1.38-5.70)。然而,在病例交叉研究中,自杀风险没有显著差异(粗 OR [cOR],0.92;95%CI,0.55-1.52),且检验效能不足。
传统病例对照研究的结果证实,与单独使用唑吡坦相比,同时使用苯二氮䓬类药物和抗抑郁药与自杀风险增加相关。然而,在个体内比较设计中,风险幅度没有显著差异。