Antipsychotic Medication Risk of Dementia and Death: A Propensity Matched Cohort Study.

Xiu R Lowe, M. Merchant, Rachel A Whitmer
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Abstract

OBJECTIVE This study aimed to compare the incidence of dementia and all-cause mortality up to 20 years post-treatment in an index non-demented cohort between antipsychotic (AP) medication treatment and non-AP treatment groups. METHOD All patients in Kaiser Permanente Northern California with a major psychiatric diagnosis between 01/01/1996 and 12/31/2000, age ≥ 50 years, and without dementia diagnosis were included. The study cohort was divided into a "user group", patients treated with AP for ≥ 365 days (n = 1,829), and a "non-user group", propensity score matched on age, sex, and race (n = 9,145). The association between AP exposure and dementia or mortality during the follow-up period (01/01/2001-12/31/2015) was evaluated using Cox proportional hazard models adjusted for psychiatric diagnosis, comorbidities, and other medications. The user group had a hazard ratio (HR) of 2.2 (CI 1.8-2.7) for dementia and 1.3 (CI 1.2-1.5) for death. The onset of dementia in the user group was significantly higher in patients aged ≤ 65 years (p < 0.001). The user group was sub-grouped into atypical, typical, and both; HR for dementia was 1.7 (CI 1.2-2.4), 2.5 (CI 1.9-3.1), and 1.8 (CI 1.4-2.4), respectively. RESULT Dementia and mortality were significantly higher in patients concurrently treated with benzodiazepine (HR 1.3; CI 1.2-1.5 and HR 1.4; CI 1.3-1.5) or tricyclic antidepressants (HR 1.2; CI 1.1-1.4 and HR 1.1; CI 1.0-1.2), respectively. CONCLUSION Our preliminary results reveal an association between AP treatment and increased rates of both dementia and mortality. Future research is needed to substantiate our current findings.
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抗精神病药物痴呆和死亡风险:一项倾向匹配队列研究。
目的:本研究旨在比较抗精神病药物治疗组和非抗精神病药物治疗组治疗后20年内痴呆和全因死亡率的发生率。方法纳入1996年1月1日至2000年12月31日期间在北加州凯撒医疗机构(Kaiser Permanente Northern California)诊断为主要精神科的患者,年龄≥50岁,无痴呆诊断。研究队列被分为“用户组”,接受AP治疗≥365天的患者(n = 1,829)和“非用户组”,倾向评分与年龄、性别和种族相匹配(n = 9,145)。在随访期间(2001年1月1日至2015年12月31日),使用经精神诊断、合并症和其他药物校正的Cox比例风险模型评估AP暴露与痴呆或死亡率之间的关系。用户组的痴呆风险比(HR)为2.2 (CI 1.8-2.7),死亡风险比(HR)为1.3 (CI 1.2-1.5)。在年龄≤65岁的患者中,用户组中痴呆的发病明显更高(p < 0.001)。用户组分为非典型、典型和两者兼而有之;痴呆的HR分别为1.7 (CI 1.2-2.4)、2.5 (CI 1.9-3.1)和1.8 (CI 1.4-2.4)。结果同时服用苯二氮卓类药物的患者痴呆和死亡率显著高于对照组(HR 1.3;CI 1.2-1.5, HR 1.4;CI 1.3-1.5)或三环类抗抑郁药(HR 1.2;CI 1.1-1.4, HR 1.1;CI 1.0-1.2)。我们的初步结果揭示了AP治疗与痴呆和死亡率增加之间的关联。需要进一步的研究来证实我们目前的发现。
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来源期刊
Current Drug Research Reviews
Current Drug Research Reviews Medicine-Psychiatry and Mental Health
CiteScore
3.70
自引率
0.00%
发文量
38
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