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The informal caregiver's lived experience of being present with a patient who receives a diagnosis of dementia: A phenomenological inquiry

机译:非正式的护理人员与患有患有痴呆症的患者的患者的生活经历:一种现象学探究

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摘要

This article describes the lived experience of informal caregivers who accompany loved ones as the loved ones receive a diagnosis of dementia. Each of 12 informal caregivers participated in a face-to-face interview that was audiotaped and transcribed. Analysis of the interview text revealed seven constituents as central to the general structure of this experience: (a) having anticipated the diagnosis; (b) feeling relief; (c) feeling the gravitas of the words; (d) grieving the loss; (e) watching for the patient's reaction; (f) accepting the diagnosis and taking action; and (g) committing to care. Implications for healthcare providers are discussed, with an emphasis on the need to be sensitive to the experience of both patients and informal caregivers when disclosing a diagnosis of dementia.
机译:本文介绍了作为亲人陪同亲人的非正式护理人员的生活体验,因为亲人受到痴呆症的诊断。 12个非正式护理人员中的每一个都参加了一个面对面的面试,曾是录音和转录的。 对面试文本的分析揭示了七个成分,作为这种经验的一般结构的核心:(a)预期诊断; (b)感到浮雕; (c)感受到这些词的贪婪; (d)悲伤的损失; (e)观察患者的反应; (f)接受诊断和采取行动; (g)致力于关心。 讨论了对医疗保健提供商的影响,重点是在揭示痴呆症的诊断时对患者和非正式护理人员的经验敏感。

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