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更安全的药物治疗以减少骨质疏松性骨折(#STOP):一项在初级医疗中由医学专家发起、药剂师主导的药物管理审查的随机对照试验研究方案。

Safer medicines To reduce falls and refractures for OsteoPorosis (#STOP): a study protocol for a randomised controlled trial of medical specialist-initiated pharmacist-led medication management reviews in primary care.

机构信息

Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.

School of Nursing and Midwifery, University of Technology Sydney Faculty of Health, Sydney, New South Wales, Australia.

出版信息

BMJ Open. 2023 Aug 24;13(8):e072050. doi: 10.1136/bmjopen-2023-072050.

Abstract

INTRODUCTION

Minimal trauma fractures (MTFs) often occur in older patients with osteoporosis and may be precipitated by falls risk-increasing drugs. One category of falls risk-increasing drugs of concern are those with sedative/anticholinergic properties. Collaborative medication management services such as Australia's Home Medicine Review (HMR) can reduce patients' intake of sedative/anticholinergics and improve continuity of care. This paper describes a protocol for an randomised controlled trial to determine the efficacy of an HMR service for patients who have sustained MTF.

METHOD AND ANALYSIS

Eligible participants are as follows: ≥65 years of age, using ≥5 medicines including at least one falls risk-increasing drug, who have sustained an MTF and under treatment in one of eight Osteoporosis Refracture Prevention clinics in Australia. Consenting participants will be randomised to control (standard care) or intervention groups. For the intervention group, medical specialists will refer to a pharmacist for HMR focused on reducing falls risk predominately through making recommendations to reduce falls risk medicines, and adherence to antiosteoporosis medicines. Twelve months from treatment allocation, comparisons between groups will be made. The main outcome measure is participants' cumulative exposure to sedative and anticholinergics, using the Drug Burden Index. Secondary outcomes include medication adherence, emergency department visits, hospitalisations, falls and mortality. Economic evaluation will compare the intervention strategy with standard care.

ETHICS AND DISSEMINATION

Approval was obtained via the New South Wales Research Ethics and Governance Information System (approval number: 2021/ETH12003) with site-specific approvals granted through Human Research Ethics Committees for each research site. Study outcomes will be published in peer-reviewed journals. It will provide robust insight into effectiveness of a pharmacist-based intervention on medicine-related falls risk for patients with osteoporosis. We anticipate that this study will take 2 years to fully accrue including follow-up.

TRIAL REGISTRATION NUMBER

ACTRN12622000261718.

摘要

简介

微小创伤性骨折(MTFs)常发生于骨质疏松症的老年患者,可能由增加跌倒风险的药物引发。引起关注的一类增加跌倒风险的药物是具有镇静/抗胆碱能特性的药物。协作药物管理服务,如澳大利亚的家庭药物审查(HMR),可以减少患者镇静/抗胆碱能药物的摄入,并提高护理的连续性。本文描述了一项随机对照试验的方案,以确定 HMR 服务对发生 MTF 的患者的疗效。

方法与分析

符合条件的参与者如下:年龄≥65 岁,使用≥5 种药物,包括至少一种增加跌倒风险的药物,发生微小创伤性骨折,并在澳大利亚的 8 个骨质疏松性骨折预防诊所之一接受治疗。同意参与的患者将被随机分配到对照组(标准护理)或干预组。对于干预组,医学专家将向药剂师转介 HMR,重点是通过减少跌倒风险药物的建议和抗骨质疏松药物的使用,来降低跌倒风险。在治疗分配后 12 个月,将对两组进行比较。主要观察指标是使用药物负担指数评估参与者对镇静剂和抗胆碱能药物的累积暴露量。次要结果包括药物依从性、急诊科就诊、住院、跌倒和死亡率。经济评估将比较干预策略与标准护理。

伦理和传播

通过新南威尔士州研究伦理和治理信息系统(批准号:2021/ETH12003)获得批准,并通过每个研究地点的人类研究伦理委员会获得特定地点的批准。研究结果将发表在同行评议的期刊上。它将为骨质疏松症患者的药物相关跌倒风险提供基于药剂师的干预的有效性的有力见解。我们预计这项研究需要 2 年时间才能完全累积,包括随访。

试验注册号

ACTRN12622000261718。

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