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一项评估社区药房出院药物核对服务对非计划住院再入院影响的随机对照试验方案——DCMedsRec试验

Protocol for a randomised controlled trial evaluating the impact of a community pharmacy discharge medication reconciliation service on unplanned hospital readmissions - The DCMedsRec trial.

作者信息

Duncan Gregory, Ngo Cathy, Fanning Laura, Taylor David A, McNamara Kevin, Caliph Suzanne, Suen Bill, Johnston Stefanie, Darzins Peteris

机构信息

Eastern Health Clinical School, Monash University, 5 Arnold St, Box Hill, VIC, 3128, Australia.

Eastern Health Clinical School, Monash University, 5 Arnold St, Box Hill, VIC, 3128, Australia; Eastern Health, 5 Arnold St, Box Hill, VIC, 3128, Australia.

出版信息

Res Social Adm Pharm. 2021 Feb;17(2):460-465. doi: 10.1016/j.sapharm.2020.03.024. Epub 2020 Apr 6.

Abstract

INTRODUCTION

A substantial proportion of hospital admissions and readmissions are directly attributable to preventable medication-related harm. Interventions that reduce these harms could avert significant suffering and healthcare costs.

OBJECTIVES

The Discharge Medications Reconciliation (DCMedsRec) trial will evaluate a structured medication reconciliation service by community pharmacists post hospital discharge on the risk of 30-day unplanned readmission. Electronic access to the Hospital Discharge Summary via My Health Record will underpin this service.

METHODS

DCMedsRec is a non-blinded randomised controlled trial of an intervention by community pharmacists within 30 days of hospital discharge in Melbourne, Australia. Patients discharged from hospital will be assessed by a hospital pharmacist for trial eligibility. If eligible, patients will be randomised to either a control or intervention group by sequentially marked sealed envelopes. Intervention patients receive an invitation to the DCMedsRec service at a participating community pharmacy, who will be reimbursed. Control patients will receive usual care. A Number Needed to Treat of 20 will require 293 DCMedsRec interventions to achieve 80% power. With a predicted 30% uptake, a minimum sample of 977 in the intervention arm is required.

OUTCOMES

The primary outcome will be the rate of 30-day unplanned hospital readmission in intervention (DCMedsRec) versus usual care groups. Secondary analyses will evaluate the economic impact of the intervention and a qualitative thematic analysis of the experience and value of the service for both patients and service providers (community pharmacists).

ANALYSIS

An intention-to-treat analysis will be used to assess intervention efficacy and results will be reported using risk ratios with 95% confidence intervals. Cost-effectiveness analysis will compare within-trial costs and outcomes of the DCMedsRec versus usual care from a health-system perspective.

TRIAL REGISTRATION AND FUNDING

This trial is registered with the Australian and New Zealand Clinical Trials Register and funded by the Australian Digital Health Agency.

摘要

引言

相当一部分住院和再次入院情况直接归因于可预防的药物相关伤害。减少这些伤害的干预措施可以避免巨大的痛苦和医疗成本。

目的

出院药物核对(DCMedsRec)试验将评估社区药剂师在出院后提供的结构化药物核对服务对30天内非计划再次入院风险的影响。通过“我的健康记录”电子访问医院出院小结将为这项服务提供支持。

方法

DCMedsRec是一项在澳大利亚墨尔本进行的非盲随机对照试验,研究社区药剂师在医院出院后30天内进行干预的效果。出院患者将由医院药剂师评估是否符合试验条件。如果符合条件,患者将通过顺序标记的密封信封随机分为对照组或干预组。干预组患者会收到参与试验的社区药房提供的DCMedsRec服务邀请,该药房将获得报销。对照组患者将接受常规护理。需治疗人数为20时,需要293次DCMedsRec干预才能达到80%的检验效能。预计接受率为30%时,干预组至少需要977个样本。

结果

主要结果将是干预组(DCMedsRec)与常规护理组的30天非计划住院再次入院率。次要分析将评估干预措施的经济影响,并对该服务对患者和服务提供者(社区药剂师)的体验和价值进行定性主题分析。

分析

将采用意向性分析来评估干预效果,结果将以风险比及95%置信区间的形式报告。成本效益分析将从卫生系统角度比较DCMedsRec与常规护理的试验内成本和结果。

试验注册与资金

本试验已在澳大利亚和新西兰临床试验注册中心注册,并由澳大利亚数字健康局资助。

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