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未经许可的“特殊”药品:运用支柱整合模型了解不同护理环境下利益相关者的观点

Unlicensed "Special" Medicines: Using the Pillar Integration Model to Understand Stakeholder Perspectives Across Care Settings.

作者信息

Wale Alesha, Mantzourani Efi

机构信息

Cardiff School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, Wales, UK.

出版信息

Integr Pharm Res Pract. 2024 Nov 27;13:209-228. doi: 10.2147/IPRP.S477087. eCollection 2024.

Abstract

BACKGROUND

The use of unlicensed medicines has been associated with safety concerns, availability and accessibility issues, and lack of integrated care across care settings.

OBJECTIVE

To understand the interaction between the views and experiences of those who prescribe, those who supply and those who receive unlicensed "special" medicines, so that factors affecting the patient journey and successful treatment can be identified and used to inform areas for change.

METHODS

A qualitative, phenomenological approach was adopted, with semi-structured interviews with prescribers, community pharmacy staff and patients. A combination of stratified, purposive, snowball and convenience sampling was used to identify participants. Interviews were analysed using reflexive thematic analysis and the findings were integrated using an adapted model of the Pillar Integration Process.

RESULTS

Three pillars were constructed after synthesising results from interviews with patients (n=4), prescribers (n=5) and pharmacy staff (n=6): the awareness of licensing status; perceptions of patient care and acceptability of unlicensed medicine use; and challenges associated with the accessibility of unlicensed medicines. The varying levels of awareness when unlicensed medicines are prescribed and the varying perceptions of responsibility and acceptability of the use of unlicensed medicines help to explain the challenges faced by participants across the patient journey, Challenges identified included understanding what unlicensed medicines are, awareness of the licensing status when unlicensed medicines are prescribed, managing care across care settings to ensure the patient is effectively treated and ensuring continuity of care for patients in the community.

CONCLUSION

The results highlight a clear need for more integrated care and support for prescribers to reduce the chances of delays between care settings, and more patient-centred care to ensure that any delays when accessing medicines do not lead to treatment disruption for the patient. The new national guidelines informed by findings of this study can support policy-makers across the globe.

摘要

背景

使用未经许可的药品会引发安全问题、供应和可及性问题,以及不同医疗机构之间缺乏综合护理的问题。

目的

了解开具、供应和使用未经许可的“特殊”药品的各方的观点和经历之间的相互作用,以便确定影响患者就医过程和成功治疗的因素,并将其用于指导变革领域。

方法

采用定性的现象学方法,对开具处方者、社区药房工作人员和患者进行半结构化访谈。使用分层、目的、滚雪球和便利抽样相结合的方法来确定参与者。采用反思性主题分析法对访谈进行分析,并使用支柱整合过程的改进模型对研究结果进行整合。

结果

在对患者(n = 4)、开具处方者(n = 5)和药房工作人员(n = 6)的访谈结果进行综合后,构建了三个支柱:对许可状态的认知;对患者护理的看法以及使用未经许可药品的可接受性;与未经许可药品可及性相关的挑战。开具未经许可药品时不同程度的认知,以及对使用未经许可药品的责任和可接受性的不同看法,有助于解释患者就医过程中参与者面临的挑战。所确定的挑战包括了解什么是未经许可的药品、开具未经许可药品时对许可状态的认知、跨医疗机构管理护理以确保患者得到有效治疗,以及确保社区患者护理的连续性。

结论

结果凸显出明显需要提供更综合的护理,并为开具处方者提供更多支持,以减少医疗机构之间延误的可能性,以及提供更多以患者为中心的护理,以确保获取药品时的任何延误不会导致患者治疗中断。本研究结果所形成的新的国家指南可为全球政策制定者提供支持。

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