改变生活计划:何时让老年癌症患者的照顾者参与预先护理计划。

IF 1.2 4区 医学 Q3 NURSING Journal of Hospice & Palliative Nursing Pub Date : 2024-02-01 DOI:10.1097/NJH.0000000000000981
Jyotsana Parajuli, Kim L Larson
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引用次数: 0

摘要

预先护理计划 (ACP) 是一个持续的过程,在这个过程中,个人会与值得信赖的护理人员和医疗服务提供者讨论并记录他们的临终偏好。照护者是参与 ACP 讨论的关键人物,因为他们会帮助所爱的人应对严重的医疗疾病。本研究的目的是考察护理者在 ACP 决策制定过程中对其癌症亲人的参与情况。研究采用了定性描述设计,并借鉴了恩格尔的生物-心理-社会模型,对北卡罗来纳州的 14 名照顾者进行了抽样调查。采用半结构化访谈指南进行了虚拟访谈。采用流行逻辑,"改变生活计划 "这一总主题由 "了解诊断 "和 "保持跟踪 "两个副主题解释。ACP 对话的时间和地点是重要的考虑因素。超过一半的参与者(64%)对 ACP 一无所知或存在误解,5 人有准确的认知。护士可以与接受过姑息关怀原则培训的社区领袖建立合作关系,尽早与社区成员开始对话。倡导团体可在社区环境中举办 "你好游戏 "等活动,以促进早期 ACP 对话。
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Changing Life Plans: When to Engage Caregivers of Older Adults With Cancer in Advance Care Planning.

Advance care planning (ACP) is a continuous process where individuals discuss and document their end-of-life preferences with trusted caregivers and health care providers. Caregivers are pivotal to include in ACP discussions because they assist loved ones to navigate serious medical illness. The purpose of this study was to examine caregivers' engagement in ACP decision making with their loved ones with cancer. A qualitative descriptive design was used, informed by Engel's biopsychosocial model, with a convenience sample of 14 caregivers in North Carolina. Virtual interviews were conducted using a semistructured interview guide. Using prevalence logic, the overarching theme of "Changing Life Plans" was explained by two subthemes, "Learning the Diagnosis" and "Keeping Them on Track." The timing and location of ACP conversations were important considerations. Over half of the participants (64%) had no knowledge or had misconceptions about ACP, and 5 had accurate knowledge. Nurses could develop partnerships with community leaders trained in palliative care principles to begin conversations early with community members. Advocacy groups might hold events, such as the Hello Game, in community settings to facilitate early ACP conversations.

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来源期刊
CiteScore
2.60
自引率
11.10%
发文量
203
审稿时长
6-12 weeks
期刊介绍: Journal of Hospice & Palliative Nursing (JHPN) is the official journal of the Hospice & Palliative Nurses Association and is the professional, peer-reviewed journal for nurses in hospice and palliative care settings. Focusing on the clinical, educational and research aspects of care, JHPN offers current and reliable information on end of life nursing. Feature articles in areas such as symptom management, ethics, and futility of care address holistic care across the continuum. Book and article reviews, clinical updates and case studies create a journal that meets the didactic and practical needs of the nurse caring for patients with serious illnesses in advanced stages.
期刊最新文献
Association News. Hospice and Palliative Nurses Association Position Statement: Medical Aid in Dying. Improving Patient-Centered Care for End-Stage Renal Disease Patients at a Community Palliative Setting. The Impact of Allyship on Minoritized Patients and Providers in Palliative Practice. True North.
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