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An exploration of the experiences of professionals supporting patients approaching the end of life in medicines management at home. A qualitative study

机译:支持患者在家中医药管理结束时患者的专业人士经验的探讨。定性学

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The management of medicines towards the end of life can place increasing burdens and responsibilities on patients and families. This has received little attention yet it can be a source of great difficulty and distress patients and families. Dose administration aids can be useful for some patients but there is no evidence for their wide spread use or the implications for their use as patients become increasing unwell. The study aimed to explore how healthcare professionals describe the support they provide for patients to manage medications at home at end of life. Qualitative interview study with thematic analysis. Participants were a purposive sample of 40 community healthcare professionals (including GPs, pharmacists, and specialist palliative care and community nurses) from across two English counties. Healthcare professionals reported a variety of ways in which they tried to support patients to take medications as prescribed. While the paper presents some solutions and strategies reported by professional respondents it was clear from both professional and patient/family caregiver accounts in the wider study that rather few professionals provided this kind of support. Standard solutions offered included: rationalising the number of medications; providing different formulations; explaining what medications were for and how best to take them. Dose administration aids were also regularly provided, and while useful for some, they posed a number of practical difficulties for palliative care. More challenging circumstances such as substance misuse and memory loss required more innovative strategies such as supporting ways to record medication taking; balancing restricted access to controlled drugs and appropriate pain management and supporting patient choice in medication use. The burdens and responsibilities of managing medicines at home for patients approaching the end of life has not been widely recognised or understood. This paper considers some of the strategies reported by professionals in the study, and points to the great potential for a more widely proactive stance in supporting patients and family carers to understand and take their medicines effectively. By adopting tailored, and sometimes, ‘outside the box’ thinking professionals can identify immediate, simple solutions to the problems patients and families experience with managing medicines.
机译:在生命结束时,药物的管理可以增加患者和家庭的负担和责任。这已经很少受到关注,但它可能是一个很大的困难和痛苦患者和家庭的来源。剂量给药艾滋病对某些患者来说有用,但没有证据表明他们广泛的频繁使用或对患者的使用影响,因为患者不适地增加。该研究旨在探讨医疗保健专业人员如何描述他们为患者提供患者的支持,以在生命结束时管理家中的药物。具有专题分析的定性访谈研究。参与者是来自两个英语县的40名社区医疗保健专业人士(包括GPS,药剂师和专业姑娘护理和社区护士)的有目的地。医疗保健专业人员报告了各种方式,他们试图支持患者服用规定的药物。虽然本文提出了一些解决方案和专业受访者报告的策略,但在更广泛的研究中,从专业和患者/家庭照顾者账户中清楚地看出,而且少数专业人士提供了这种支持。提供的标准解决方案包括:合理化药物数量;提供不同的配方;解释哪些药物是有什么药物和如何最好服用它们。还定期提供剂量给药艾滋病,同时对一些有用,它们为姑息治疗提供了许多实际困难。更具挑战性的情况,如物质滥用和记忆力损失需要更多的创新策略,例如支持培养药物的方法;平衡限制对受控药物的准入和适当的疼痛管理和在药物使用中的患者选择。在接近生命结束的患者中,在家中管理药物的负担和责任尚未得到广泛认可或理解。本文考虑了研究中专业人员报告的一些策略,并指出了在支持患者和家庭护理人员了解并有效地采取药物的巨大潜力。通过采用量身定制,有时候,“箱子外”思维专业人员可以识别立即的,简单的解决方案,对患者和管理药物的经验。

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