Department of Pharmaceutical Health Outcomes and Policy, College of Pharmacy, University of Houston, Houston, Texas, USA.
Department of Pharmacy Practice and Translational Research, College of Pharmacy, University of Houston, Houston, Texas, USA.
Pharmacotherapy. 2024 Oct;44(10):782-793. doi: 10.1002/phar.4610. Epub 2024 Sep 17.
Both Alzheimer's disease (AD) and deliriogenic medications increase the risk of delirium in older adults. This study examined the association between delirium and the subsequent monthly use of anticholinergic, sedative, and opioid medications in the 1 year after delirium in older adults with AD.
This comparative interrupted time series analysis involved adults (aged 65 years and older) with a diagnosis of AD initiating on cholinesterase inhibitors (ChEIs) based on 2013-2017 Medicare data. Separate patient-level segmented regression models were used for each outcome to evaluate changes in the cumulative anticholinergic burden (CAB), sedative load, and opioid load after the delirium/index event using a 12-month baseline and follow-up period among patients who had a delirium event and those without delirium (control group). Propensity score-based stabilized weights were utilized to balance baseline factors in the delirium and control groups.
The study included 80,019 older adults with AD with incident ChEI use; 17.11% had delirium. There was an immediate decline in monthly CAB after the delirium event (mean estimate -0.86, p-value: 0.01) compared to the control group. A similar decline was observed when examining the sedative load (-0.06, p-value: 0.002) after the delirium event. However, there was no decline in opioid load (-0.50, p-value: 0.18). In the long term, CAB (0.13; p-value: <0.0001), sedative load (0.01; p-value: <0.001), and opioid load (0.07; p-value: 0.006) increased over the 1-year post-delirium period in the delirium group compared to those without delirium.
This study found the burden of deliriogenic medications over the 1-year follow-up showed increasing trends in older adults with AD, even though there was some level shift in CAB and sedative load after the delirium event.
阿尔茨海默病(AD)和致谵妄药物都会增加老年人发生谵妄的风险。本研究旨在探讨谵妄与 AD 老年患者谵妄后 1 年内每月使用抗胆碱能药物、镇静剂和阿片类药物之间的关联。
本项对比性中断时间序列分析纳入了根据 2013-2017 年医疗保险数据开始使用胆碱酯酶抑制剂(ChEI)的年龄在 65 岁及以上的 AD 成人患者。分别使用每个结局的患者水平分段回归模型,评估谵妄/指数事件后 12 个月基线和随访期间,谵妄组和无谵妄组(对照组)的累积抗胆碱能负担(CAB)、镇静负荷和阿片类药物负荷的变化。使用基于倾向评分的稳定权重来平衡谵妄组和对照组的基线因素。
本研究纳入了 80019 例使用 ChEI 治疗的 AD 老年患者,其中 17.11%发生了谵妄。与对照组相比,谵妄事件后 CAB 每月立即下降(平均估计值-0.86,p 值:0.01)。在谵妄事件后,镇静负荷也观察到类似的下降(-0.06,p 值:0.002)。然而,阿片类药物负荷没有下降(-0.50,p 值:0.18)。在长期随访中,与无谵妄患者相比,谵妄组在谵妄后 1 年内 CAB(0.13;p 值:<0.0001)、镇静负荷(0.01;p 值:<0.001)和阿片类药物负荷(0.07;p 值:0.006)持续增加。
本研究发现,在 AD 老年患者中,即使在谵妄事件后 CAB 和镇静负荷出现一定程度的水平转移,在 1 年的随访期间,致谵妄药物的负担仍呈上升趋势。