痴呆症患者和照护者是否得到了他们所需要的?社会护理和照护者需求评估中的障碍。

Dementia (London, England) Pub Date : 2024-05-01 Epub Date: 2024-03-01 DOI:10.1177/14713012241237673
Clarissa Giebel, James Watson, Julie Dickinson, Mark Gabbay, Kath Halpin, Andrew Harding, Caroline Swarbrick
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引用次数: 0

摘要

背景:痴呆症患者和无偿照护者需要通过社会护理或照护者需求评估,才能获得和接受补贴或全额资助的社会护理。由于之前没有相关证据,本定性研究旨在深入了解社会护理或照护者需求评估的获取途径、接受评估和进行评估的经验以及社会护理的获取途径:方法:在 2023 年 4 月至 8 月期间,对居住或工作在英格兰的痴呆症患者的无偿照护者和进行社会照护或照护者需求评估的专业人士进行了远程访谈,了解他们的经历。我们与两名无酬照护者共同制作了主题指南,并协助他们对匿名记录誊本进行编码。采用主题分析法对数据进行分析:27 名无报酬照护者(n = 21)和专业人员(n = 6)参与了研究。共产生了四个主题:(1) 获得需求评估的问题,而非评估过程;(2) 对需求评估以及医疗和社会护理系统的了解;(3) 无酬照护者的期望;以及 (4) 评估后未满足的需求。无酬照护者及其痴呆症患者亲属遇到的最突出障碍是对需求评估的认识和获得需求评估的机会。无酬照护者大多不知道需求评估的存在和权利,有时他们会意识到自己在不知情的情况下参加了需求评估。专业人员描述了他们的时间压力以及服务机构缺乏财政资源的情况:为了更好地为痴呆症患者提供护理和对照护者的支持,获得需求评估的途径需要更加清晰,同时加强医疗和社会护理之间的整合与沟通。
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Do people with dementia and carers get what they need? Barriers in social care and carers needs assessments.

Background: People with dementia and unpaid carers need to go through a social care or carers needs assessment to access and receive subsidised or fully-funded social care. With no previous evidence, this qualitative study aimed to provide insights into the access to, experiences of receiving and conducting social care or carers needs assessments, and access to social care.

Methods: Unpaid carers of people with dementia and professionals conducting social care or carers needs assessment living or working in England were interviewed remotely about their experiences between April and August 2023. Topic guides were co-produced with two unpaid carers, and both were supported to code anonymised transcripts. Thematic analysis was used to analyse the data.

Findings: Twenty-seven unpaid carers (n = 21) and professionals (n = 6) participated. Four themes were generated: (1) Issues with accessing needs assessments, not the process; (2) Knowledge of needs assessments and the health and social care system; (3) Expectations of unpaid carers; and (4) Post-assessment unmet needs. The most prominent barriers unpaid carers and their relatives with dementia encountered were awareness of and access to needs assessment. Unpaid carers were mostly unaware of the existence and entitlement to a needs assessment, and sometimes realised they had participated in one without their knowledge. Professionals described the pressures on their time and the lack of financial resources within services.

Conclusions: To facilitate improved access to dementia care and support for carers, the pathway to accessing needs assessments needs to be clearer, with better integration and communication between health and social care.

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