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首页> 外文期刊>BMC Palliative Care >Context, mechanisms and outcomes in end-of-life care for people with advanced dementia: family carers perspective
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Context, mechanisms and outcomes in end-of-life care for people with advanced dementia: family carers perspective

机译:晚期痴呆症患者临终关怀的背景,机制和结果:家庭照顾者的观点

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Keeping people living with advanced dementia in their usual place of residence is becoming a key governmental goal but to achieve this, family carers and health care professionals must negotiate how to provide optimal care. Previously, we reported a realist analysis of the health care professional perspective. Here, we report on family carer perspectives. We aimed to understand the similarities and differences between the two perspectives, gain insights into how the interdependent roles of family carers and HCPs can be optimised, and make recommendations for policy and practice. Qualitative study using a realist approach in which we used the criteria from guidance on optimal palliative care in advanced dementia to examine key contexts, mechanisms and outcomes highlighted by family carers. The themes and views of family caregivers resonate with those of health care professionals. Their overlapping anxieties related to business-driven care homes, uncertainty of families when making EOL decisions and the importance of symptom management referring to contexts, mechanisms and outcomes, respectively. Contexts specific to family carers were ad hoc information about services, dementia progression and access to funding. Not all family carers identified dementia as terminal, but many recognised the importance of continuity of care and knowing the wishes of the person with dementia. New mechanisms included specific resources for improving EOL care and barriers to discussing and planning for future care. Family carers identified the importance of comfort, being present, the meeting of basic care needs and feeling the right decisions have been made as good outcomes of care. Family carers and health care professionals share similar concerns about the challenges to good EOL dementia care. Better understanding of the effects of dementia at the advanced stages would improve confidence in EOL care and reduce uncertainty in decision making for family carers and health care professionals.
机译:将患有高龄痴呆症的人留在其通常的住所已成为政府的主要目标,但要实现这一目标,家庭护理人员和医疗保健专业人员必须协商如何提供最佳护理。以前,我们报告了对医疗保健专业人员观点的现实主义分析。在这里,我们将介绍家庭照顾者的观点。我们旨在了解两种观点之间的异同,了解如何优化家庭照顾者和HCP的相互依存关系,并提出政策和实践建议。使用现实主义方法进行的定性研究,在该研究中,我们使用了晚期痴呆患者最佳姑息治疗指南中的标准,以检查家庭护理人员强调的关键情况,机制和结果。家庭护理人员的主题和观点与卫生保健专业人员的主题和观点共鸣。他们重叠的焦虑与商业驱动的护理院,做出EOL决策时家庭的不确定性以及症状管理对上下文,机制和结果的重要性有关。家庭护理者的具体情况是有关服务,痴呆症进展和获得资金的临时信息。并非所有家庭护理人员都将痴呆症视为终末期,但许多人意识到持续护理的重要性以及了解痴呆症患者的意愿。新的机制包括改善EOL护理的特定资源以及讨论和规划未来护理的障碍。家庭看护者认为舒适,到场,满足基本护理需求以及感觉做出正确的决定作为护理的良好结果的重要性。家庭护理人员和卫生保健专业人员对良好的EOL痴呆症护理面临的挑战也有类似的担忧。更好地了解晚期痴呆症的效果将提高人们对EOL护理的信心,并减少家庭护理人员和医疗保健专业人员决策的不确定性。

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