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钙通道阻滞剂和利尿剂处方级联与不良事件的关联:一项基于人群的队列研究。

Association of a calcium channel blocker and diuretic prescribing cascade with adverse events: A population-based cohort study.

机构信息

Women's Age Lab and Women's College Research Institute, Women's College Hospital, Toronto, Ontario, Canada.

ICES, Toronto, Ontario, Canada.

出版信息

J Am Geriatr Soc. 2024 Feb;72(2):467-478. doi: 10.1111/jgs.18683. Epub 2023 Nov 27.

Abstract

BACKGROUND

Prescribing cascades occur when a drug adverse event is misinterpreted as a new medical condition and a second, potentially unnecessary drug, is prescribed to treat the adverse event. The population-level consequences of prescribing cascades remain unknown.

METHODS

This population-based cohort study used linked health administrative databases in Ontario, Canada. The study included community-dwelling adults, 66 years of age or older with hypertension and no history of heart failure (HF) or diuretic use in the prior year, newly dispensed a calcium channel blocker (CCB). Individuals subsequently dispensed a diuretic within 90 days of incident CCB dispensing were classified as the prescribing cascade group, and compared to those not dispensed a diuretic, classified as the non-prescribing cascade group. Those with and without a prescribing cascade were matched one-to-one on the propensity score and sex. The primary outcome was a serious adverse event (SAE), which was the composite of emergency room visits and hospitalizations in the 90-day follow-up period. We estimated hazard ratios (HRs) with 95% confidence intervals (CI) for SAE using an Andersen-Gill recurrent events regression model.

RESULTS

Among 39,347 older adults with hypertension and no history of HF who were newly dispensed a CCB, 1881 (4.8%) had a new diuretic dispensed within 90 days after CCB initiation. Compared to the non-prescribing cascade group, those in the prescribing cascade group had higher rates of SAEs (HR: 1.21, 95% CI: 1.02-1.43).

CONCLUSIONS

The CCB-diuretic prescribing cascade was associated with an increased rate of SAEs, suggesting harm beyond prescribing a second drug therapy. Our study raises awareness of the downstream impact of the CCB-diuretic prescribing cascade at a population level and provides an opportunity for clinicians who identify this prescribing cascade to review their patients' medications to determine if they can be optimized.

摘要

背景

当药物不良反应被误解为新的医学病症,并且开出第二种潜在不必要的药物来治疗不良反应时,就会发生处方级联。处方级联对人群的影响仍不清楚。

方法

这是一项基于人群的队列研究,使用了加拿大安大略省的相关健康管理数据库。该研究纳入了年龄在 66 岁及以上、患有高血压且在过去一年中没有心力衰竭(HF)或利尿剂使用史的社区居住成年人,新开出了钙通道阻滞剂(CCB)。在 CCB 配药后 90 天内配给利尿剂的患者被归类为处方级联组,与未配给利尿剂的患者进行比较,归类为非处方级联组。对有和没有处方级联的患者进行倾向评分和性别匹配。主要结局是严重不良事件(SAE),即在 90 天随访期间急诊就诊和住院的综合结果。我们使用 Andersen-Gill 复发性事件回归模型估计了 95%置信区间(CI)内 SAE 的风险比(HR)。

结果

在 39347 名年龄在 66 岁及以上、患有高血压且没有 HF 病史的成年人中,有 1881 名(4.8%)在 CCB 开始后 90 天内新开出了利尿剂。与非处方级联组相比,处方级联组的 SAE 发生率更高(HR:1.21,95%CI:1.02-1.43)。

结论

CCB-利尿剂处方级联与 SAE 发生率的增加有关,这表明除了开出第二种药物治疗之外,还存在其他危害。我们的研究提高了人们对 CCB-利尿剂处方级联在人群层面的下游影响的认识,并为识别出这种处方级联的临床医生提供了机会,以便审查他们的患者的药物,以确定是否可以优化药物。

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