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超越简单计划:与心力衰竭风险患者对话的存在维度。

Beyond Simple Planning: Existential Dimensions of Conversations With Patients at Risk of Dying From Heart Failure.

机构信息

Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada; Centre for Education Research and Innovation, McMaster University, Hamilton, Ontario, Canada; Department of Anesthesia & Perioperative Medicine, practicing in Palliative Care, McMaster University, Hamilton, Ontario, Canada.

Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada; Department of Family Medicine, McMaster University, Hamilton, Ontario, Canada.

出版信息

J Pain Symptom Manage. 2017 Nov;54(5):637-644. doi: 10.1016/j.jpainsymman.2017.07.041. Epub 2017 Aug 5.

Abstract

CONTEXT

Despite the recent promotion of communication guides to improve decision making with patients nearing the end of their lives, these conversations remain challenging. Deeper and more comprehensive understanding of communication barriers that undermine discussions and decisions with patients at risk of dying from heart failure (HF) is vital for informing communication in health care.

OBJECTIVES

To explore experiences and perspectives of patients with advanced HF, their caregivers, and providers, regarding conversations for patients at risk of dying from HF.

METHODS

Following Research Ethics Board approval, index patients with advanced HF (New York Heart Association III or IV) and consenting patient-identified care team members were interviewed. A team sampling unit was formed when the patient plus at least two additional team members participated in interviews. Team members included health professionals (e.g., cardiologist, family physician, HF nurse practitioner, social worker, and specialists, such as respirologist, nephrologist, palliative care physician), family caregivers (e.g., daughter, spouse, roommate, close friend), and community members (e.g., minister, neighbor, regular taxi driver). Our data set included 209 individual interviews clustered into 50 team sampling units at five sites from three Canadian provinces. Key informants, identified as practicing experts in the field, reviewed our initial findings with attention to relevance to practice as a form of triangulation. Iterative data collection and analysis followed constructivist grounded theory procedures with sensitizing concepts drawn from complexity theory. To ensure confidentiality, all participants were given a pseudonym.

RESULTS

Participants' reports of their perceptions and experiences of conversations related to death and dying suggested two main dimensions of such conversations: instrumental and existential. Instrumental dimensions included how these conversations were planned and operationalized as well as the triggers and barriers to these discussions. Existential dimensions of these conversations included evasive maneuvers, powerful emotions, and the phenomenon of death without dying. Existential dimensions appeared to have a basis in issues of mortality and could strongly influence conversations related to death and dying.

CONCLUSION

Conversations for patients at risk of dying from HF have both instrumental and existential dimensions, in which routines and relationships are inseparable. Our current focus on the instrumental aspects of these conversations is necessary but insufficient. The existential dimensions of conversations related to death are profound and may explain why these conversations have struggled to achieve their desired effect. To improve this communication, we need to also attend to existential dimensions, particularly in terms of their impact on the occurrence of these conversations, the nature of relationships and responses within these conversations, and the fluidity of meaning within these conversations.

摘要

背景

尽管最近推广了沟通指南以改善临终患者的决策,但这些对话仍然具有挑战性。深入了解可能因心力衰竭(HF)而死亡的患者的沟通障碍,并全面了解这些障碍,对于为医疗保健中的沟通提供信息至关重要。

目的

探讨患有晚期 HF 的患者、他们的照顾者和提供者对有风险死于 HF 的患者的对话的经验和观点。

方法

在获得研究伦理委员会批准后,对患有晚期 HF(纽约心脏协会 III 或 IV 级)的索引患者和同意的患者确定的护理团队成员进行了采访。当患者加上至少两名额外的团队成员参与访谈时,形成了一个团队采样单元。团队成员包括卫生专业人员(例如心脏病专家、家庭医生、HF 执业护士、社会工作者以及专家,例如呼吸科医生、肾脏病专家、姑息治疗医生)、家庭照顾者(例如女儿、配偶、室友、密友)和社区成员(例如部长、邻居、常规出租车司机)。我们的数据集中包括 209 次个人访谈,这些访谈聚类为来自三个加拿大省份的五个地点的 50 个团队采样单元。关键知情人被确定为该领域的实践专家,他们根据复杂性理论的敏感性概念,审查了我们的初步发现,重点关注与实践的相关性,以此作为三角测量的一种形式。按照建构主义扎根理论程序进行迭代数据收集和分析,该理论的启发概念来自复杂性理论。为了确保保密性,所有参与者都使用了化名。

结果

参与者对与死亡和临终相关的对话的看法和经验报告表明,这些对话有两个主要维度:工具性和存在性。工具性维度包括这些对话的计划和运作方式,以及这些讨论的触发因素和障碍。这些对话的存在性维度包括回避策略、强烈的情绪以及死亡而不死的现象。存在性维度似乎基于死亡率问题,并且可能强烈影响与死亡和临终相关的对话。

结论

有风险死于 HF 的患者的对话具有工具性和存在性两个维度,其中常规和关系是不可分割的。我们目前对这些对话的工具性方面的关注是必要的,但还不够。与死亡相关的对话的存在性方面是深刻的,可能解释了为什么这些对话难以达到预期的效果。为了改善这种沟通,我们还需要关注存在性方面,特别是要关注它们对这些对话发生的影响、这些对话中的关系和回应的性质,以及这些对话中意义的流动性。

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