痴呆症患者的健康和社会护理需求:澳大利亚吉普斯兰维多利亚地区痴呆症支持定性研究。

IF 2 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Rural and remote health Pub Date : 2024-01-01 Epub Date: 2024-01-18 DOI:10.22605/RRH8244
Maria H Garrett, Denise Azar, Dianne Goeman, Mishael Thomas, Elizabeth A Craig, Darryl Maybery
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引用次数: 0

摘要

导言:目前缺乏有关痴呆症患者及其照护者经历的信息,尤其是在农村和地区。了解他们的经历有助于找出医疗系统中的不足和未满足的需求,并提高对痴呆症患者的护理质量和效果。这项研究旨在提高我们对痴呆症支持需求的认识。这包括痴呆症患者以及为痴呆症患者提供非正式或正式支持的人员获得医疗和社会护理服务及支持的情况:对来自澳大利亚维多利亚州吉普斯兰地区的 26 名了解痴呆症护理知识的参与者进行了访谈。有针对性的抽样调查涉及有生活经验的人、照护者/家庭成员以及提供痴呆症照护和社会服务的医疗专业人员。讨论围绕参与者对支持服务的体验、诊断过程以及他们认为需要改进的服务和支持展开。采用框架法对数据进行了专题分析:访谈数据表明,许多痴呆症患者及其照护者的需求目前没有得到满足。这些主题包括:获得服务和支持(包括初级和专科护理)的机会有限,这往往受到缺乏护理选择知识、难以驾驭系统和资金模式等障碍的影响,从而导致诊断和获得专科服务方面的延误;缺乏使痴呆症患者能够 "生活得很好 "的整体护理;以及专业人士和社区对痴呆症缺乏了解而产生的耻辱感。以关系为中心的护理被认为是改善痴呆症患者生活的一种方式:需要改进的关键领域包括:提高社区对痴呆症和当地可用服务的认识;为获得早期痴呆症诊断提供更多支持;为驾驭系统提供更多帮助,尤其是在诊断后立即提供帮助;以及在需要时更容易获得适当的家庭支持服务。其他建议还包括:在资助模式的支持下,在各种环境中提供以人为本的护理服务;为医疗专业人员和护理人员提供更多的教育和沟通技巧培训;以及为护理人员提供更多的支持并提高他们对护理人员的认可度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Health and social care needs of people living with dementia: a qualitative study of dementia support in the Victorian region of Gippsland, Australia.

Introduction: There is a lack of information about the experiences of people living with dementia and their carers, especially in rural and regional areas. Understanding these experiences helps to identify gaps and unmet needs within the health system and improve quality of care and outcomes for people living with dementia. The aim of this study was to improve our knowledge of dementia support needs. This included access to health and social care services and supports for people living with dementia and those who provide informal or formal support to someone living with dementia.

Methods: Interviews were conducted with 26 participants from the Gippsland region of Victoria, Australia with knowledge of dementia care. Purposive sampling engaged people with lived experience, carers/family members and health professionals delivering dementia care and social services. Discussions centred around participants' experiences of support services, the diagnosis process and what they thought was needed to improve the services and supports offered. Thematic analysis of the data was undertaken using the framework method.

Results: The interview data indicated that the needs of many people living with dementia and their carers were not currently being met. The themes were limited access to services and supports, including primary and specialist care, often impacted by lack of knowledge of care options, difficulty navigating the system and funding models as a barrier, leading to delays in getting a diagnosis and accessing specialist services; lack of holistic care to enable people living with dementia to 'live well'; and stigma impacted by a lack of knowledge of dementia among professionals and in the community. Relationship-centred care was described as a way to improve the lives of people living with dementia.

Conclusion: Key areas for improvement include increasing community awareness of dementia and available local services, more support to obtain an early dementia diagnosis, increased help to navigate the system, especially immediately after diagnosis, and easier access to appropriate home support services when they are needed. Other recommendations include person-centred care across settings - supported by funding models, more education and communication skills training for health professionals and care staff - and greater support for and increased recognition of carers.

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来源期刊
Rural and remote health
Rural and remote health Rural Health-
CiteScore
2.00
自引率
9.50%
发文量
145
审稿时长
8 weeks
期刊介绍: Rural and Remote Health is a not-for-profit, online-only, peer-reviewed academic publication. It aims to further rural and remote health education, research and practice. The primary purpose of the Journal is to publish and so provide an international knowledge-base of peer-reviewed material from rural health practitioners (medical, nursing and allied health professionals and health workers), educators, researchers and policy makers.
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