Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Durham VA Geriatric Research Education and Clinical Center (GRECC), Durham, North Carolina, USA.
J Am Geriatr Soc. 2021 Nov;69(11):3212-3224. doi: 10.1111/jgs.17377. Epub 2021 Jul 22.
BACKGROUND/OBJECTIVES: Unintentional falls are a leading cause of injury for older adults, and evidence is needed to understand modifiable risk factors. We evaluated 1-year fall-related fracture risk and whether dispensing of medications with anticholinergic/sedating properties is temporally associated with an increased odds of these fractures.
A retrospective cohort study with nested self-controlled analyses conducted between January 1, 2014, and December 31, 2016.
Twenty percent nationwide, random sample of US Medicare beneficiaries.
New users of medications with anticholinergic/sedating properties who were 66+ years old and had Medicare Parts A, B, and D coverage but no claims for medications with anticholinergic/sedating properties in the year before initiation were eligible.
We followed new users of medications with anticholinergic/sedating properties until first non-vertebral, fall-related fracture (primary outcome), Medicare disenrollment, death, or end of study data. We estimated the 1-year risk with corresponding 95% confidence intervals (CIs) of first fracture after new use. We applied the self-controlled case-crossover and case-time-control designs to estimate odds ratios (ORs) and 95% CIs by comparing anticholinergic and/or sedating medication exposure (any vs. none) during a 14-day hazard period preceding the fracture to exposure to these medications during an earlier 14-day control period.
A total of 1,097,989 Medicare beneficiaries initiated medications with anticholinergic/sedating properties in the study period. The 1-year cumulative incidence of fall-related fracture, accounting for death as a competing risk, was 5.0% (95% CI: 5.0%-5.0%). Using the case-crossover design (n = 41,889), the adjusted OR for the association between anticholinergic/sedating medications and fractures was 1.03 (95% CI: 0.99, 1.08). Accounting for the noted temporal trend using the case-time-control design (n = 209,395), the adjusted OR was 1.60 (95% CI: 1.52, 1.69).
Use of anticholinergic/sedating medication was temporally associated with an increased odds of fall-related fractures. Patients and their healthcare providers should consider pharmacologic and non-pharmacologic treatments for the target condition that are safer.
背景/目的:意外跌倒导致老年人受伤的主要原因,需要有证据来了解可改变的危险因素。我们评估了 1 年内与跌倒相关的骨折风险,以及配药时使用具有抗胆碱能/镇静作用的药物是否与这些骨折的发生几率增加有关。
2014 年 1 月 1 日至 2016 年 12 月 31 日期间进行的回顾性队列研究和嵌套的自我对照分析。
美国医疗保险的 20%的全国范围内的随机抽样受益人群。
年龄在 66 岁及以上、有医疗保险 A、B 和 D 部分覆盖,但在开始使用具有抗胆碱能/镇静作用的药物之前的一年内没有这些药物索赔的新使用者。
我们随访了新使用具有抗胆碱能/镇静作用的药物的患者,直到首次非椎骨、跌倒相关骨折(主要结果)、医疗保险退出、死亡或研究数据结束。我们估计了新使用后 1 年内首次骨折的风险,以及相应的 95%置信区间(CI)。我们应用自我对照病例交叉和病例时间对照设计,通过比较骨折前 14 天危险期内的抗胆碱能和/或镇静药物暴露(任何 vs. 无)与更早的 14 天对照期内的这些药物暴露,来估计比值比(OR)和 95%CI。
在研究期间,共有 1097989 名医疗保险受益人开始使用具有抗胆碱能/镇静作用的药物。考虑到死亡是一种竞争风险,跌倒相关骨折的 1 年累积发生率为 5.0%(95%CI:5.0%-5.0%)。使用病例交叉设计(n=41889),抗胆碱能/镇静药物与骨折之间的调整后 OR 为 1.03(95%CI:0.99,1.08)。使用病例时间对照设计(n=209395)考虑到这一注意到的时间趋势,调整后 OR 为 1.60(95%CI:1.52,1.69)。
使用抗胆碱能/镇静药物与跌倒相关骨折的发生几率增加有关。患者及其医疗保健提供者应考虑针对目标疾病的更安全的药物和非药物治疗。