美国老年人的性别、种族/民族和年龄与开始服用慢性高风险药物之间的关系。

Katharina Tabea Jungo, Niteesh K Choudhry, Alexander Chaitoff, Julie C Lauffenburger
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引用次数: 0

摘要

背景:高危药物的使用与不良事件风险的增加有关,但人们对主要人口群体长期使用高危药物的情况知之甚少。我们旨在研究老年人的年龄、性别、种族/民族与新的高风险药物长期使用之间的关系:在这项回顾性队列研究中,我们分析了加入一家全国性医疗保险公司的年龄≥65 岁的老年人的数据,他们在 2017 年至 2022 年期间开始使用 16 种高风险药物类别中的高风险药物。我们使用广义估计方程来估计社会人口学分类与起始后长期使用高风险药物(180 天内≥2 次服药,用药量≥90 天)之间的关联。我们根据患者的社会人口学特征和临床特征对分析进行了调整,并添加了种族/民族、性别和年龄的三方交互项,以探讨结果是否会因种族/民族、年龄和性别的不同分组而有所变化:在 2,751,069 名患者(平均年龄:74 岁 [SD = 7],72%为白人,60%为女性)中,有 406,075 人(15%)成为≥1 种高风险药物的新慢性使用者。与白人老年人相比,亚裔(RR = 0.81,95% CI:0.79-0.84)、黑人(RR = 0.92,95% CI:0.90-0.94)和西班牙裔(RR = 0.85,95% CI:0.83-0.86)老年人成为新的慢性用药者的风险较低。与女性相比,男性的风险更高(RR = 1.09,95% CI:1.08-1.10)。年龄与新的高风险慢性病用药并无明显关联(≥75 岁:RR = 1.00,95% CI:1.00-1.01)。我们观察到一些药物类别之间存在差异,如苯二氮卓类药物、第一代抗组胺药物和抗心律失常药物,非白人老年人使用这些药物的风险较高。同时具有特定的年龄、性别和种族/民族特征会降低成为新的慢性用药者的风险(例如,西班牙裔/女性/65-74 岁:RR = 0.96,95% CI:0.94-0.99):不同社会人口特征的老年人新的慢性高危用药情况各不相同,这表明有必要采取个性化的用药优化方法,并更好地了解获得医疗保健方面的系统性障碍如何影响老年人高危用药的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations between sex, race/ethnicity, and age and the initiation of chronic high-risk medication in US older adults.

Background: High-risk medication use is associated with an increased risk of adverse events, but little is known about its chronic utilization by key demographic groups. We aimed to study the associations between age, sex, and race/ethnicity with new chronic use of high-risk medications in older adults.

Methods: In this retrospective cohort study, we analyzed data from older adults aged ≥65 years enrolled in a national health insurer who started a high-risk medication between 2017 and 2022 across 16 high-risk medication classes. We used generalized estimating equations to estimate the associations between sociodemographic classifications and the onset of chronic high-risk medication use after initiation (≥90 days' supply across ≥2 fills within 180 days). We adjusted the analyses for sociodemographic and clinical patient characteristics and added three-way interaction terms for race/ethnicity, sex, and age to explore whether the outcome varied across different subgroups of race/ethnicity, age, and sex.

Results: Across 2,751,069 patients (mean age: 74 years [SD = 7], 72% White, 60% Female), 406,075 (15%) became new chronic users of ≥1 high-risk medication. Compared to White older adults, Asian (RR = 0.81, 95% CI: 0.79-0.84), Black (RR = 0.92, 95% CI: 0.90-0.94), and Hispanic (RR = 0.85, 95% CI: 0.83-0.86) older adults had a lower risk of becoming new chronic users. Men had a higher risk compared to women (RR = 1.09, 95% CI: 1.08-1.10). Age was not significantly associated with new chronic high-risk medication use (≥75 years: RR = 1.00, 95% CI: 1.00-1.01). We observed differences across some medication classes, like benzodiazepines, first-generation antihistamines, and antimuscarinics for which non-White older adults were at a higher risk. The joint presence of specific age, sex, and race/ethnicity characteristics decreased the risk of becoming a new chronic user (e.g., Hispanic/Female/65-74 years: RR = 0.96, 95% CI: 0.94-0.99).

Conclusions: New chronic high-risk medication use varied across older adults by sociodemographic characteristics, suggesting the need to individualize medication optimization approaches and better understand how systematic barriers in access to health care may influence differences in high-risk medication use in older adults.

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