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痴呆症患者的照护环境过渡:当前和前任照护伙伴的定性观点。

Care Setting Transitions for People With Dementia: Qualitative Perspectives of Current and Former Care Partners.

机构信息

UC Berkeley-UCSF Joint Medical Program, University of California at Berkeley, Berkeley, CA, USA.

School of Medicine, University of California at San Francisco, San Francisco, CA, USA.

出版信息

Am J Hosp Palliat Care. 2023 Dec;40(12):1310-1316. doi: 10.1177/10499091231155601. Epub 2023 Feb 2.

Abstract

Care partners (CP) of people with dementia (PWD) report that decisions about care setting are aided by the support of healthcare providers. However, providers are often underprepared to offer adequate counseling. This qualitative study aimed to identify what support from providers will assist CPs in making decisions related to care setting throughout the dementia journey. We conducted semi-structured interviews with current CPs of PWD and former CPs of decedents. We utilized the constant comparative method to identify themes regarding preferences around care setting as the PWD progressed from diagnosis to end-of-life. Participants were 31 CPs, including 16 current and 15 former CPs. CPs had a mean age of 67 and were primarily white (n = 23/31), female (n = 21/31), and spouses (n = 24/31). Theme 1: Current CPs discussed overwhelming uncertainty pertaining to care setting, expressing "I don't know when I need to plan on more care," and a desire to understand "what stage we are at." Theme 2: Later in the disease, former CPs wanted guidance from healthcare providers on institutional placement ("I sure would've loved some help finding better places") or support to stay in the home ("a doctor had to come to the house"). CPs want early, specific guidance from healthcare providers related to transitions between home and long-term care. Early in the disease course, counseling geared toward prognosis and expected disease course helps CPs make plans. Later, caregivers want help identifying locations or institutionalization or finding home care resources.

摘要

照护者(CP)报告称,痴呆症患者(PWD)的医疗服务提供者的支持有助于他们做出有关护理地点的决策。然而,提供者通常准备不足,无法提供足够的咨询。这项定性研究旨在确定提供者提供哪些支持将有助于 CP 在整个痴呆症旅程中做出与护理地点相关的决策。我们对目前的 PWD 照护者和已故 PWD 的前照护者进行了半结构式访谈。我们采用恒定性比较方法,确定参与者在 PWD 从诊断到临终期间对护理地点偏好的主题。参与者有 31 名 CP,包括 16 名现任 CP 和 15 名前 CP。CP 的平均年龄为 67 岁,主要是白人(n = 23/31),女性(n = 21/31),配偶(n = 24/31)。主题 1:目前的 CP 讨论了有关护理地点的压倒性不确定性,他们表示“我不知道何时需要计划更多的护理”,并希望了解“我们处于哪个阶段”。主题 2:在疾病后期,前 CP 希望医疗保健提供者在机构安置方面提供指导(“我真的很希望有人帮助找到更好的地方”)或支持他们留在家里(“医生必须到家里来”)。CP 希望医疗保健提供者在家庭和长期护理之间的过渡早期提供有关过渡的具体指导。在疾病早期,针对预后和预期疾病过程的咨询可以帮助 CP 制定计划。之后,护理人员希望帮助确定地点或机构化或寻找家庭护理资源。

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