Hollis Jean, Grayson David, Forrester Loelle, Brodaty Henry, Touyz Stephen, Cumming Robert
School of Psychology, University of Sydney, Sydney, Australia.
Am J Geriatr Psychiatry. 2007 Nov;15(11):932-41. doi: 10.1097/JGP.0b013e31813547ca.
To establish the instantaneous relative risk (RR) of death associated with individual antipsychotic drugs, carbamazepine and sodium valproate for those 65 years and older.
Subjects dispensed antipsychotic drugs, sodium valproate or carbamazepine in 2003 or 2004 were analyzed as incident (N = 16,634) or prevalent (N = 9,831) users. Survival curves, mortality rates, and Cox proportional hazards models over two time periods were used to explore risk of death. The models were adjusted for age, sex, residential status, and psychotropic and medical drug dispensing. Olanzapine subjects were the reference group in the Cox regression. Subanalyses were performed for incident subjects with more than 30 days of follow-up and those dispensed cholinesterase inhibitors.
In the adjusted Cox proportional hazards models, haloperidol dispensing was consistently associated with an increased risk of death compared with olanzapine users (relative risk [RR] for incident users: 2.26, 95% confidence intervals (CI): 2.08-2.47; Wald statistic: 345.36, df = 1, p < or =0.001). There was some evidence of decreased survival with dispensing of higher haloperidol doses, although confounding by medical comorbidity cannot be excluded. Chlorpromazine (RR: 1.39, 95% CI: 1.15-1.67; Wald statistic: 12.08, df = 1, p <0.001) and risperidone (RR: 1.23, 95% CI: 1.07-1.40; Wald statistic: 9.12, df = 1, p = 0.003) dispensing were associated with increased risk of death in incident users.
These results should be interpreted cautiously because haloperidol and chlorpromazine are used in broader clinical contexts. However, in the absence of data from randomized trials, the safety profile of haloperidol should not be assumed to be benign. Antipsychotic drugs should not be studied as an aggregated group because their associated risks are not uniform.
确定65岁及以上人群使用个别抗精神病药物、卡马西平和丙戊酸钠后的即时相对死亡风险(RR)。
将2003年或2004年使用抗精神病药物、丙戊酸钠或卡马西平的受试者作为新使用者(N = 16,634)或现使用者(N = 9,831)进行分析。采用两个时间段的生存曲线、死亡率和Cox比例风险模型来探讨死亡风险。模型针对年龄、性别、居住状况以及精神药物和医疗药物的配给情况进行了调整。在Cox回归中,以奥氮平使用者作为参照组。对随访时间超过30天的新使用者以及使用胆碱酯酶抑制剂的使用者进行了亚组分析。
在调整后的Cox比例风险模型中,与奥氮平使用者相比,使用氟哌啶醇始终与死亡风险增加相关(新使用者的相对风险[RR]:2.26,95%置信区间[CI]:2.08 - 2.47;Wald统计量:345.36,自由度 = 1,p≤0.001)。有一些证据表明,使用较高剂量氟哌啶醇会降低生存率,尽管不能排除合并症的混杂影响。使用氯丙嗪(RR:1.39,95% CI:1.15 - 1.67;Wald统计量:12.08,自由度 = 1,p <0.001)和利培酮(RR:1.23,95% CI:1.07 - 1.40;Wald统计量:9.12,自由度 = 1,p = 0.003)与新使用者的死亡风险增加相关。
由于氟哌啶醇和氯丙嗪的临床应用范围更广,这些结果应谨慎解读。然而,在缺乏随机试验数据的情况下,不应假定氟哌啶醇的安全性良好。抗精神病药物不应作为一个整体进行研究,因为它们的相关风险并不一致。