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Caregivers’ interactions with health care services – Mediator of stress or added strain? Experiences and perceptions of informal caregivers of people with dementia – A qualitative study

机译:护理人员与医疗保健服务的互动 - 压力或增加压力的介质? 对痴呆症的非正式照顾者的经验与看法 - 一个定性研究

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Background: There are an estimated 46.8 million people worldwide living with dementia in 2015, being cared for usually by family members or friends (informal caregivers). The challenges faced by informal caregivers often lead to increased levels of stress, burden and risk of care-recipient institutionalisation. Aim: The overarching aim of this study was to explore the experiences and perceptions of informal caregivers of people with dementia when interacting with the health care system, and whether the support received acted as a mediator of caregiver stress. The secondary aim was to investigate healthcare professionals’ views and current practice regarding people with dementia and their interactions with informal caregivers. Method: We employed a qualitative research design, using focus groups and one face-to-face interview with a purposive sample of informal caregivers and healthcare professionals in Lincolnshire, UK. Data were collected between March and July 2015. We used the stress-process model of stress in caregivers as a theoretical framework. Results: We interviewed 18 caregivers and 17 healthcare professionals. Five themes, mapped to the stress-process in caregivers’ model, captured the main challenges faced by caregivers and the type of support they wanted from health care services. Primary stressors included the challenge of diagnosing dementia; caregivers’ needs and expectations of an in-depth knowledge and understanding of dementia from healthcare professionals; and need for carer education. Secondary role strain included lack of support and mismatch of communication and expectations. Caregiver involvement in monitoring care and disease was a potential mediator tool. Conclusions: Fragmentation of dementia care services, lack of training for healthcare professionals and the dearth of information for caregivers means health care services are only partially fulfilling a support role. In turn, lack of support may be intensifying caregiver stress leading to worsening in their health and well-being; thus, potentially increasing the risk of institutionalisation of their care-recipient.
机译:背景:2015年估计有4680万人患有痴呆症的痴呆症,通常由家庭成员或朋友(非正式护理人员)感到关怀。非正式护理人员面临的挑战往往导致压力,负担和护理受援人士制度化的风险增加。目的:本研究的总体目标是探讨与医疗保健系统互动时痴呆症的非正式护理人员的经验和看法,以及是否被收到的支持作为护理人员压力的调解员。二次目的是调查医疗保健专业人员的观点和目前对痴呆症人民的看法以及与非正式护理人员的互动。方法:我们采用了一个定性研究设计,使用焦点小组和一个面对面的采访,与英国林肯郡的非正式护理人员和医疗保健专业人士的目的地采访。 2015年3月至7月之间收集了数据。我们在护理人员中使用了压力的压力过程模型作为理论框架。结果:我们采访了18名护理人员和17名医疗专业人士。五个主题,映射到护理人员模型中的压力过程,捕获了护理人员面临的主要挑战以及他们想要的医疗保健服务的支持类型。主要压力源包括诊断痴呆症的挑战;照顾者对医疗专业人士的深入知识和对痴呆症的理解的需求和期望;并需要护理人员教育。次要角色应变包括缺乏沟通和期望的支持和不匹配。护理人员参与监测护理和疾病是潜在的调解工具。结论:痴呆症护理服务的破碎化,医疗保健专业人员缺乏培训以及护理人员信息的缺乏意味着医疗保健服务仅部分履行支持作用。反过来,缺乏支持可能会加强护理人员压力,导致健康和福祉恶化;因此,可能增加了他们的护理受援人员制度化的风险。

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