Department of Pharmaceutical Health Outcomes and Policy (FC, MLJ, HC, RRA), College of Pharmacy, University of Houston, Houston, TX.
The University of Texas Health Science Center (HMH), Houston, TX; Division of Geriatric and Palliative Medicine (HMH), McGovern Medical School, Houston, TX.
Am J Geriatr Psychiatry. 2020 Oct;28(10):1079-1088. doi: 10.1016/j.jagp.2020.01.193. Epub 2020 Feb 7.
This study examined the risk of all-cause-mortality in patients with Parkinson's Disease (PD) and comorbid depression using inappropriate atypical antipsychotics (AAPs), based on the 2015 American Geriatrics Society Beers criteria.
A retrospective analysis of 2007-2010 Minimum Data Set linked Medicare data was conducted using a propensity-matched approach. The cohort included PD patients aged 65 years or older without schizophrenia or bipolar disorder who started AAPs. All patients had a diagnosis of comorbid depression. Risk of 6-month all-cause-mortality was compared across appropriate AAPs (aripiprazole, clozapine, or quetiapine) and inappropriate AAPs (olanzapine, asenapine, brexpiprazole, iloperidone, lurasidone, paliperidone, risperidone, or ziprasidone) using robust Cox regression models involving the matched cohort.
All-cause mortality rate was 15.65% in appropriate AAP group (n = 6,038) and 16.91% in inappropriate AAP group (n = 6,038) over 6-month follow-up in the matched cohort. The robust Cox proportional hazards models revealed increased risk of all-cause mortality (hazard ratio [HR] 1.13 [95% confidence interval {CI}: 1.01-1.28)] for patients who used inappropriate compared to appropriate AAPs. Risk of death was also higher for risperidone compared to quetiapine (HR: 1.20 [95% CI: 1.03-1.40]) in sensitivity analysis. However, there was a significant relationship between pneumonia and death in all analyses. The impact of inappropriate AAP use on mortality was not significant when pneumonia was modeled as a mediator.
Inappropriate AAP use is associated with a higher risk of all-cause-mortality in older patients with PD which is mainly mediated by pneumonia. Therefore, inappropriate AAP use should be avoided to improve quality of care in PD.
本研究基于 2015 年美国老年医学会 Beers 标准,使用不适当的非典型抗精神病药物(AAPs),检查帕金森病(PD)合并抑郁患者的全因死亡率风险。
使用倾向匹配方法对 2007-2010 年最低数据组链接医疗保险数据进行回顾性分析。该队列包括年龄在 65 岁或以上、无精神分裂症或双相情感障碍且开始使用 AAP 的 PD 患者。所有患者均有合并抑郁的诊断。使用稳健的 Cox 回归模型比较了合适的 AAP(阿立哌唑、氯氮平或喹硫平)和不合适的 AAP(奥氮平、阿塞那平、布瑞哌唑、依匹哌唑、鲁拉西酮、帕利哌酮、利培酮或齐拉西酮)在匹配队列中 6 个月全因死亡率的风险。
在匹配队列中,合适的 AAP 组(n=6038)的全因死亡率为 15.65%,而不合适的 AAP 组(n=6038)为 16.91%。稳健的 Cox 比例风险模型显示,与使用合适的 AAP 相比,使用不合适的 AAP 的患者全因死亡率风险增加(风险比[HR]1.13[95%置信区间{CI}:1.01-1.28])。在敏感性分析中,与喹硫平相比,利培酮的死亡风险也更高(HR:1.20[95%CI:1.03-1.40])。然而,在所有分析中,肺炎与死亡之间存在显著关系。当肺炎作为中介变量建模时,不适当的 AAP 使用对死亡率的影响并不显著。
在老年 PD 患者中,使用不适当的 AAP 与全因死亡率风险增加相关,这主要是由肺炎介导的。因此,应避免不适当的 AAP 使用,以提高 PD 的护理质量。