Acceptability of a cross-sectoral hospital pharmacist intervention for patients in transition between hospital and general practice: a mixed methods study.

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Therapeutic Advances in Drug Safety Pub Date : 2023-12-15 eCollection Date: 2023-01-01 DOI:10.1177/20420986231213714
Charlotte Arp Sørensen, Linda Jeffery, Klaus Roelsgaard, Solveig Gram, Jannik Falhof, Philipp Harbig, Charlotte Olesen
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引用次数: 0

Abstract

Background and objective: Drug-related problems (DRPs) are often seen when a patient is transitioning from one healthcare sector to another, for example, when a patient moves from the hospital to a General Practice (GP) setting. This transition creates an opportunity for information on medication changes and follow-up plans to be lost. A cross-sectoral hospital pharmacist intervention was developed and pilot-tested in a large GP clinic. The intervention included medication history, medication reconciliation, medication review, follow-up telephone calls, identification of possible DRPs and communication with the GP. It is unknown whether the intervention is transferable to other GP clinics. The aim of the study was to explore similarities and differences between GP clinics in descriptive data and intervention acceptability.

Methods: A convergent mixed methods study design was used. The intervention was tested in four GP clinics with differing characteristics. Quantitative data on the GP clinics, patients and pharmacist activities were collected. Qualitative data on the acceptability were collected through focus group interviews with general practitioners, nurses and pharmacists. The Theoretical Framework of Acceptability was used.

Results: Overall, the intervention was found acceptable and relevant by all. There were differences between the GP clinics in terms of size, daily physician work form and their use of pharmacists for ad hoc tasks. There were similarities in patient characteristics across GP clinics. Therefore, the intervention was found equally relevant for all of the clinics. Shared employment with unique access to health records in both sectors was important in the identification and resolution of DRPs. Economy was a barrier for further implementation.

Conclusions: The intervention was found acceptable and relevant by all; therefore, it was considered transferable to other GP clinics. Hospital pharmacists were perceived to be relevant healthcare professionals to be utilized in GP, in hospitals and in the cross-sectoral transition of patients.

跨部门医院药剂师对医院和全科诊所之间过渡病人的干预措施的可接受性:一项混合方法研究。
背景和目的:当病人从一个医疗部门转到另一个医疗部门时,例如,当病人从医院转到全科医生(GP)诊所时,经常会出现与药物相关的问题(DRPs)。这种过渡会造成用药变化和后续计划信息的丢失。我们开发了一种跨部门医院药剂师干预措施,并在一家大型全科医生诊所进行了试点测试。干预措施包括询问用药史、用药核对、用药检查、电话随访、识别可能的 DRP 以及与全科医生沟通。目前尚不清楚该干预措施是否可用于其他全科医生诊所。本研究旨在探讨全科医生诊所在描述性数据和干预措施可接受性方面的异同:方法:采用聚合混合方法研究设计。干预措施在四家具有不同特点的全科医生诊所进行了测试。收集了有关全科医生诊所、患者和药剂师活动的定量数据。通过对全科医生、护士和药剂师进行焦点小组访谈,收集了有关可接受性的定性数据。采用了可接受性理论框架:结果:总体而言,所有人都认为干预措施是可接受的,并且具有相关性。全科医生诊所在规模、医生日常工作形式以及使用药剂师完成临时任务方面存在差异。各全科医生诊所的病人特征具有相似性。因此,干预措施对所有诊所都同样适用。在两个部门共享工作岗位并能唯一访问健康记录,这对识别和解决 DRP 问题非常重要。经济因素是进一步实施的障碍:结论:所有人都认为该干预措施是可接受的,并且具有相关性;因此,该干预措施可推广到其他全科医生诊所。医院药剂师被认为是可用于全科医生、医院和跨部门病人转诊的相关医护专业人员。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapeutic Advances in Drug Safety
Therapeutic Advances in Drug Safety Medicine-Pharmacology (medical)
CiteScore
6.70
自引率
4.50%
发文量
31
审稿时长
9 weeks
期刊介绍: Therapeutic Advances in Drug Safety delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies pertaining to the safe use of drugs in patients. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in drug safety, providing a forum in print and online for publishing the highest quality articles in this area. The editors welcome articles of current interest on research across all areas of drug safety, including therapeutic drug monitoring, pharmacoepidemiology, adverse drug reactions, drug interactions, pharmacokinetics, pharmacovigilance, medication/prescribing errors, risk management, ethics and regulation.
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