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Providing support to surrogate decision-makers for people living with dementia: Healthcare professional, organisational and community responsibilities

机译:为患有痴呆症的人提供支持:医疗保健专业,组织和社区责任

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The prevalence of dementia will continue to increase with the ageing of the population. Many people living with dementia will reach a stage where surrogate decision-makersmostly family carerswill need to make a range of decisions on their behalf. The aim of this study was to learn from surrogate decision-makers how they can be most effectively supported in this role. The study employed a qualitative design using semi-structured face-to-face or telephone interviews with a purposive sample of 34 surrogate decision-makers of people living with dementia. Transcripts of participant interviews were reviewed using a thematic approach to analysis. Four main themes were identified from this analysis: needing greater community awareness of dementia and its impact; intervening early in cognitive decline; relying on health professionals for ongoing support; and seeking and using support from wherever is relevant for each person. Based on this analysis and a review of the literature, we propose a wholistic set of recommendations for the support of surrogate decision-makers. Healthcare professionals need to help family carers understand the likely trajectory of dementia, including the significance of surrogate decision-making. They can support the person living with dementia and their surrogates to undertake advance care planning and they can act as empathic guides during this process. Health and community care organisations need to provide a key worker model wherever possible so that the person living with dementia and their surrogate decision-maker do not have to seek support from multiple staff members or organisations. Carer support programmes can routinely include information and resources about surrogate decision-making. Community and government organisations can help people prepare for the possibility of becoming surrogate decision-makers by promoting a greater public awareness and understanding of both dementia and advance care planning.
机译:痴呆症的患病率将随着人口老龄化而继续增加。许多患有痴呆症的人将达到一个阶段,代理决策者最多的家庭护理需要代表他们的一系列决定。本研究的目的是从代理决策者中学到如何在这一角色中最有效地支持它们。该研究采用了一种使用半结构化面对面或电话采访的定性设计,其有34名患有痴呆症的人的替代决策者的目的样本。使用主题方法进行审查参与者访谈的成绩单。从这个分析中确定了四个主要主题:需要更大的社区对痴呆症及其影响的意识;早期在认知下降中介入;依靠卫生专业人士进行持续支持;并寻求和使用支持从任何人都与每个人相关。根据这一分析和对文献的审查,我们向代理决策者的支持提出了一系列的一系列建议。医疗保健专业人员需要帮助家庭照顾者了解痴呆症的可能轨迹,包括代理决策的意义。他们可以支持患有痴呆症的人和他们的代理人承接先进的护理计划,他们可以在此过程中充当异常指南。健康和社区护理组织需要尽可能提供关键工人模型,以便与痴呆症及其代理决策者居住的人不必寻求多个工作人员或组织的支持。 Carer支持计划可以常规地包括关于代理决策的信息和资源。社区和政府组织可以帮助人们通过促进对痴呆症和经济保健规划的更大的公众意识和理解来准备成为代理决策者的可能性。

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