Wang Philip S, Schneeweiss Sebastian, Avorn Jerry, Fischer Michael A, Mogun Helen, Solomon Daniel H, Brookhart M Alan
Department of Psychiatry, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02120, USA.
N Engl J Med. 2005 Dec 1;353(22):2335-41. doi: 10.1056/NEJMoa052827.
Recently, the Food and Drug Administration (FDA) issued an advisory stating that atypical antipsychotic medications increase mortality among elderly patients. However, the advisory did not apply to conventional antipsychotic medications; the risk of death with these older agents is not known.
We conducted a retrospective cohort study involving 22,890 patients 65 years of age or older who had drug insurance benefits in Pennsylvania and who began receiving a conventional or atypical antipsychotic medication between 1994 and 2003. Analyses of mortality rates and Cox proportional-hazards models were used to compare the risk of death within 180 days, less than 40 days, 40 to 79 days, and 80 to 180 days after the initiation of therapy with an antipsychotic medication. We controlled for potential confounding variables with the use of traditional multivariate Cox models, propensity-score adjustments, and an instrumental-variable analysis.
Conventional antipsychotic medications were associated with a significantly higher adjusted risk of death than were atypical antipsychotic medications at all intervals studied (< or =180 days: relative risk, 1.37; 95 percent confidence interval, 1.27 to 1.49; <40 days: relative risk, 1.56; 95 percent confidence interval, 1.37 to 1.78; 40 to 79 days: relative risk, 1.37; 95 percent confidence interval, 1.19 to 1.59; and 80 to 180 days: relative risk, 1.27; 95 percent confidence interval, 1.14 to 1.41) and in all subgroups defined according to the presence or absence of dementia or nursing home residency. The greatest increases in risk occurred soon after therapy was initiated and with higher dosages of conventional antipsychotic medications. Increased risks associated with conventional as compared with atypical antipsychotic medications persisted in confirmatory analyses performed with the use of propensity-score adjustment and instrumental-variable estimation.
If confirmed, these results suggest that conventional antipsychotic medications are at least as likely as atypical agents to increase the risk of death among elderly persons and that conventional drugs should not be used to replace atypical agents discontinued in response to the FDA warning.
最近,美国食品药品监督管理局(FDA)发布一项公告称,非典型抗精神病药物会增加老年患者的死亡率。然而,该公告不适用于传统抗精神病药物;这些较老药物的死亡风险尚不清楚。
我们进行了一项回顾性队列研究,涉及宾夕法尼亚州22890名65岁及以上有药物保险福利且在1994年至2003年间开始接受传统或非典型抗精神病药物治疗的患者。使用死亡率分析和Cox比例风险模型,比较在开始使用抗精神病药物治疗后180天内、少于40天、40至79天以及80至180天内的死亡风险。我们通过使用传统多元Cox模型、倾向评分调整和工具变量分析来控制潜在的混杂变量。
在所有研究的时间段内(≤180天:相对风险为1.37;95%置信区间为1.27至1.49;<40天:相对风险为1.56;95%置信区间为1.37至1.78;40至79天:相对风险为1.37;95%置信区间为1.19至1.59;80至180天:相对风险为1.27;95%置信区间为1.14至1.41)以及根据是否患有痴呆症或是否居住在养老院定义的所有亚组中,与非典型抗精神病药物相比,传统抗精神病药物的调整后死亡风险显著更高。风险增加最大的情况发生在治疗开始后不久以及使用较高剂量传统抗精神病药物时。在使用倾向评分调整和工具变量估计进行的验证性分析中,与非典型抗精神病药物相比,传统抗精神病药物相关的风险增加仍然存在。
如果得到证实,这些结果表明传统抗精神病药物至少与非典型药物一样有可能增加老年人的死亡风险,并且不应使用传统药物来替代因FDA警告而停用的非典型药物。