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衰弱的长期护理居民中降压药物的停用(OptimizeBP):一项前瞻性、随机、开放标签实用试验的方案。

Antihypertensive deprescribing in frail long-term care residents (OptimizeBP): protocol for a prospective, randomised, open-label pragmatic trial.

机构信息

Department of Family Medicine, University of Alberta, Edmonton, Alberta, Canada

Pragmatic Trials Collaborative, University of Alberta, Edmonton, Alberta, Canada.

出版信息

BMJ Open. 2024 Aug 29;14(8):e084619. doi: 10.1136/bmjopen-2024-084619.

Abstract

INTRODUCTION

Although antihypertensive medication use is common among frail older adults, observational studies in this population suggest blood pressure (BP) lowering may convey limited benefit and perhaps even harm. This protocol describes an antihypertensive deprescribing trial in frail older adults powered for mortality and morbidity outcomes.

METHODS AND ANALYSIS

Prospective, parallel, randomised, open-label pragmatic trial. Long-term care (LTC) residents ≥70 years of age, diagnosed with hypertension, with mean systolic BP <135 mm Hg, ≥1 daily antihypertensive medication and no history of congestive heart failure. 18 LTC facilities in Alberta, Canada, with eligible residents identified using electronic health services data. All non-opted-out eligible residents are randomised centrally by a provincial health data steward to either usual care, or continually reducing antihypertensives provided an upper systolic threshold of 145 mm Hg is not exceeded. Deprescribing is carried out by pharmacists/nurse practitioners, using an investigator-developed algorithm. Provincial healthcare databases tracking hospital, continuing care and community medical services. All-cause mortality. Composite of all-cause mortality or all-cause unplanned hospitalisation/emergency department visit. All-cause unplanned hospitalisation/emergency department visit, non-vertebral fracture, renal insufficiency and cost of care. Also, as assessed roughly 135-days postrandomisation, fall in the last 30 days, worsening cognition, worsening activities of daily living and skin ulceration. Number of daily antihypertensive medications (broken down by antihypertensive class) and average systolic and diastolic BP over study duration. Cox proportional hazards survival analysis. The trial will continue until observation of 247 primary outcome events has occurred. Enrolment is ongoing with ~400 randomisations to date (70% female, mean age 86 years).

ETHICS AND DISSEMINATION

Ethics approval was obtained from the University of Alberta Health Ethics Review Board (Pro00097312) and results will be published in a peer-reviewed journal.

TRIAL REGISTRATION NUMBER

NCT05047731.

摘要

简介

尽管降压药物在体弱的老年患者中广泛应用,但该人群中的观察性研究表明,降压治疗可能带来有限的益处,甚至可能有害。本方案描述了一项针对体弱老年患者的降压药物停药试验,该试验针对死亡率和发病率结局进行了充分设计。

方法和分析

前瞻性、平行、随机、开放标签实用试验。长期护理(LTC)机构≥70 岁,诊断为高血压,平均收缩压<135mmHg,≥1 种降压药物,且无充血性心力衰竭病史。在加拿大阿尔伯塔省 18 家 LTC 机构中,使用电子健康服务数据识别符合条件的居民。所有非选择退出的合格居民均由省级卫生数据管理员进行中央随机分组,分别接受常规护理或持续减少降压药物治疗,但收缩压上限为 145mmHg 不超标。停药由药剂师/执业护士根据研究者制定的算法进行。省级医疗保健数据库跟踪医院、持续护理和社区医疗服务。全因死亡率。全因死亡率或全因非计划性住院/急诊就诊的复合结局。全因非计划性住院/急诊就诊、非脊椎骨折、肾功能不全和医疗费用。还评估了大约随机分组后 135 天的跌倒情况、过去 30 天的认知功能恶化、日常生活活动能力恶化和皮肤溃疡。研究期间的每日降压药物数量(按降压药物类别细分)和平均收缩压和舒张压。Cox 比例风险生存分析。试验将继续进行,直到观察到 247 例主要结局事件发生。目前正在进行登记,迄今已完成约 400 例随机分组(70%为女性,平均年龄 86 岁)。

伦理和传播

已获得阿尔伯塔大学健康伦理审查委员会的批准(Pro00097312),研究结果将发表在同行评议的期刊上。

试验注册号

NCT05047731。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bb9/11404250/fed3e65954ae/bmjopen-14-8-g001.jpg

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