Cardiff School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, Wales, UK.
University Library Services, Cardiff University, Cardiff, Wales, UK.
Res Social Adm Pharm. 2023 Jul;19(7):1025-1041. doi: 10.1016/j.sapharm.2023.04.120. Epub 2023 Apr 20.
Unlicensed medicines are used across the UK to treat an individual's clinical needs when there are no appropriate licensed alternatives. Patients, carers and parents have reported facing challenges with unlicensed medicines at the points of transfer of care between settings, a key time when medication errors may occur. There is little known about the patient journey as a whole, or the factors affecting patient care when receiving an unlicensed medicine.
A systematic review of UK literature to better understand factors that affect the entire patient journey from the decision to initiate treatment with an unlicensed medicine to the point at which treatment is supplied through a community pharmacy or ends.
Scopus, OVID EMCARE, EMBASE, OVID Medline ALL, CINAHL, Web of Science and Joanna Briggs Institute were searched from 1968 (introduction of the Medicines Act) until November 2020, using the PRISMA guidelines. Narrative synthesis of UK studies was employed to analyse descriptive and qualitative data on any reported findings that would impact the patient journey or care related to the use of unlicensed medicines, and any described barriers or enablers.
Forty-five studies met criteria for final inclusion, with high levels of heterogeneity in terms of designs and methods. Specific challenges that were seen to impact the continuity of care across care settings, patient safety and provision of patient-centred care included diversity of clinical needs and impact of patient population age; healthcare professional awareness and acceptability of the use of unlicensed medicines; the hierarchical structure of the NHS; inconsistent doses and formulations with varying bioequivalence; patient/parent/carer/public awareness of unlicensed medicines use and perceived acceptability.
This review identified a clear need for consistent information to be provided to healthcare professional and patients alike to support the safe and effective use of unlicensed medicines across care settings.
在英国,当没有合适的许可替代药物时,未经许可的药物被用于治疗个人的临床需求。患者、护理人员和家长报告称,在医疗机构之间的护理交接点面临着未经许可的药物使用的挑战,这是药物错误可能发生的关键时期。人们对整个患者就医过程或在接受未经许可的药物时影响患者护理的因素知之甚少。
对英国文献进行系统回顾,以更好地了解从决定开始使用未经许可的药物治疗到通过社区药房供应或结束治疗的整个患者就医过程中影响因素。
从 1968 年(药品法出台)到 2020 年 11 月,使用 PRISMA 指南,在 Scopus、OVID EMCARE、EMBASE、OVID Medline ALL、CINAHL、Web of Science 和 Joanna Briggs Institute 上进行了搜索。采用英国研究的叙述性综合方法,分析了与使用未经许可的药物相关的任何报告结果对患者就医过程或护理的影响,以及任何描述的障碍或促进因素的描述性和定性数据。
45 项研究符合最终纳入标准,在设计和方法方面存在高度异质性。被认为影响跨护理环境的连续性、患者安全和提供以患者为中心的护理的具体挑战包括临床需求的多样性和患者人群年龄的影响;医疗保健专业人员对使用未经许可的药物的意识和接受程度;NHS 的等级结构;剂量和配方不一致,生物等效性不同;患者/家长/护理人员/公众对未经许可的药物使用的认识和可接受程度。
本综述确定了明确的需求,需要向医疗保健专业人员和患者提供一致的信息,以支持在跨护理环境中安全有效地使用未经许可的药物。