Development and trial of an instrument to evaluate accredited pharmacists' clinical home medicines review reports in Australia

IF 1 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmacy Practice and Research Pub Date : 2022-10-06 DOI:10.1002/jppr.1829
Marea Patounas PhD, BPharm, MPS, AACPA, SFHEA, AFHEA (Indigenous), Esther T. L. Lau PhD, BPharm (Hons), GCResComm, GradCertAcadPrac, SFHEA, AFHEA (Indigenous), MPS, Deborah Rigby BPharm, GradDipClinPharm, AdvPracPharm, FPS, FSHP, FACP, FASCP FAICD, Vincent Chan PhD, BPharm, MPH, MPS, Lisa M. Nissen PhD, BPharm, AdvPracPharm, FPS, FHKAPh, FSHP
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引用次数: 2

Abstract

In Australia, clinical reports are written by an accredited pharmacist following in-home patient consultations as part of a home medicines review (HMR). These reports communicate clinical findings and recommendations to the patient's general practitioner to optimise medicines and improve patient health. However, it is unknown if clinical HMR reports adhere to practice guidelines. This study aimed to develop an instrument from Australian practice guidelines, and then test the instrument by evaluating a small sample of clinical HMR reports written by accredited pharmacists. An instrument was developed from a consolidation of HMR practice guidelines and then applied to a small sample of de-identified clinical HMR reports provided by accredited pharmacists. The instrument developed contained 30 criteria for clinical HMR report writing, and 20 HMR reports were evaluated from 12 accredited pharmacists. Seven of the 30 criteria were met by all clinical HMR reports evaluated (were consumer-focused, documented a medicines list, medicines strengths, medicines directions, medication-related problems, and included both evidence-based and clinical recommendations for optimising medicines management). However, of the 20 HMR reports evaluated only 30% (n = 6) documented the general practitioner's reason for HMR referral, 60% (n = 12) detailed allergies/adverse drug reactions, 50% (n = 10) documented an adherence statement, and 20% (n = 4) documented vaccination status. Clinical HMR reports evaluated in this small study were aligned with practice guidelines for some criteria. Future research is warranted in a larger study to further investigate clinical HMR report writing adherence to practice guidelines in Australia.

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澳大利亚注册药剂师临床家庭药物审查报告评估工具的开发和试验
在澳大利亚,作为家庭药物审查(HMR)的一部分,临床报告由注册药剂师在家庭患者咨询后撰写。这些报告将临床发现和建议传达给患者的全科医生,以优化药物并改善患者健康。然而,尚不清楚临床HMR报告是否符合实践指南。本研究旨在根据澳大利亚执业指南开发一种仪器,然后通过评估由注册药剂师撰写的临床HMR报告的小样本来测试该仪器。该仪器是在HMR实践指南的基础上开发的,然后应用于认证药剂师提供的一小部分未鉴定的临床HMR报告样本。开发的仪器包含30项临床HMR报告撰写标准,12名注册药剂师对20份HMR报告进行了评估。所有评估的临床HMR报告都满足了30项标准中的7项(以消费者为中心,记录了药物清单、药物优势、药物方向、药物相关问题,并包括基于证据和优化药物管理的临床建议)。然而,在评估的20份HMR报告中,只有30%(n=6)记录了全科医生转诊HMR的原因,60%(n=12)记录了详细的过敏/药物不良反应,50%(n=10)记录了依从性声明,20%(n=4)记录了疫苗接种状态。在这项小型研究中评估的临床HMR报告与一些标准的实践指南一致。未来的研究需要在一项更大规模的研究中进行,以进一步调查澳大利亚临床HMR报告写作对实践指南的遵守情况。
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来源期刊
Journal of Pharmacy Practice and Research
Journal of Pharmacy Practice and Research Health Professions-Pharmacy
CiteScore
1.60
自引率
9.50%
发文量
68
期刊介绍: The purpose of this document is to describe the structure, function and operations of the Journal of Pharmacy Practice and Research, the official journal of the Society of Hospital Pharmacists of Australia (SHPA). It is owned, published by and copyrighted to SHPA. However, the Journal is to some extent unique within SHPA in that it ‘…has complete editorial freedom in terms of content and is not under the direction of the Society or its Council in such matters…’. This statement, originally based on a Role Statement for the Editor-in-Chief 1993, is also based on the definition of ‘editorial independence’ from the World Association of Medical Editors and adopted by the International Committee of Medical Journal Editors.
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