生命终结时的叙事认同:存在主义视角下尊严治疗访谈的定性分析。

IF 2.5 2区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Pia Devuyst, Richard E Leiter, Aimee Milliken, Josef Jenewein, David Blum, Annina Seiler
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引用次数: 0

摘要

背景:面对绝症和死亡的前景会严重破坏一个人的认同感、生命的意义和目的,导致存在的痛苦,增加绝望、抑郁症状和死亡焦虑。目的:本研究探讨叙事方法如何减轻面临死亡和临终的个体的存在性痛苦,促进情感愈合,巩固身份。具体而言,本研究旨在(1)应用Ricoeur的自我和身份框架,分析尊严治疗(DT)遗留文献中反映的身份维度;(2)加深对存在主义痛苦与认同的关系及其转化为有意义适应的可能性的理解;(3)将这些发现综合成一个生命终结时叙事认同的概念模型。方法:采用MAXQDA软件对32份DT访谈进行定性数据分析。采用归纳范畴发展方法构建了一个包含身份关键维度的三层编码系统。在利科的自我和身份框架的基础上,运用解释学和存在现象学的方法,在脆弱、痛苦、失去和生命即将结束的背景下,加深对自我和身份的生活经历和叙事重建的理解。结果:叙事认同的维度包括“出身”、“家庭”、“运动”、“社会”、“工作”、“娱乐”、“破坏”、“当下体验”、“感受”、“自我意识”和“未来”。对病人叙述的分析产生了对存在的痛苦的深入理解,以及在生命结束时的真实性,完整性和整体性的对比体验。叙事作品在重申自我和身份认同的同时减轻存在主义痛苦的三个核心机制:(1)培养愈合联系并拥抱希望;(2)寻找连贯和意义建构;(3)内在成长与转化。这些发现为生命终结时叙事认同的概念模型的发展提供了信息。结论:面对死亡和濒死是一项挑战,但它可能是增强自我意识、自我成长和向更真实转变的催化剂。讲故事是一种简单而有力的工具,它可以在失去控制和无能为力的时期重新获得叙事身份,减轻存在的痛苦。我们的“生命终结时的叙事身份模型”说明了叙事工作如何促进深度工作,通过这种方式,治疗联系和希望可以被接受,使人们能够基于意义适应临终疾病,从而使个人能够保持控制感、能动性和自主性,即使面对自己的死亡。试验注册:本研究已在临床试验注册中心注册(ClinicalTrials.gov -方案记录NCT02646527;注册日期:04/01/2016)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Narrative identity at the end of life: a qualitative analysis of dignity therapy interviews from an existential perspective.

Background: Confronting terminal illness and the prospect of death and dying can severely undermine an individual's sense of identity, meaning and purpose in life, leading to existential suffering, increasing hopelessness, depressive symptoms, and death anxieties.

Objectives: This study explored how narrative approaches can alleviate existential suffering, promote emotional healing, and consolidate identity for individuals confronted with death and dying. Specifically, the study aimed to (1) analyze dimensions of identity reflected in Dignity Therapy (DT) legacy documents from a randomized controlled trial, applying Ricoeur's framework of selfhood and identity; (2) deepen the understanding of existential suffering in relation to identity and its potential transformation into meaningful adaptation; and (3) synthesize these findings into a conceptual Model of Narrative Identity at the End of Life.

Methods: Thirty-two DT interviews were analyzed using MAXQDA software for qualitative data analysis. An inductive category development approach was employed to construct a three-tiered coding system capturing key dimensions of identity. Drawing on Ricoeur's framework of selfhood and identity, a hermeneutic and existential-phenomenological approach was employed to deepen understanding of the lived experiences and narrative reconstruction of self and identity in the context of vulnerability, suffering, loss, and the approaching end of life.

Results: The identified dimensions of narrative identity included "origin", "family", "movement", "societal", "work", "recreation", "disruption", "experience of the now", "feelings", "sense of self", and "future". Analysis of patients' narratives yielded an in-depth understanding of existential suffering, as well as the contrasting experiences of authenticity, integrity, and wholeness at the end of life. Three core mechanisms emerged through which narrative work may mitigate existential suffering while reaffirming selfhood and identity: (1) cultivation healing connections and embracing hope; (2) the search for coherence and meaning-making; and (3) inner growth and transformation. These findings informed the development of a conceptual Model of Narrative Identity at the End of Life.

Conclusions: Confronting death and dying is challenging, yet it may serve as a catalyst for increased self-awareness, self-growth, and transformation towards greater authenticity. Storytelling is a simple yet powerful tool for reclaiming narrative identity and alleviating existential suffering during a time marked by loss of control and powerlessness. Our Model of Narrative Identity at the End of Life illustrates how narrative work facilitates depth work, through which healing connections and hope can be embraced, enabling meaning-based adaptation to terminal illness, thereby empowering individuals to retain a sense of control, agency, and autonomy, even in the face of their own mortality.

Trial registration: This study was registered with Clinical Trial Registry (ClinicalTrials.gov - Protocol Record NCT02646527; date of registration: 04/01/2016).

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来源期刊
BMC Palliative Care
BMC Palliative Care HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.60
自引率
9.70%
发文量
201
审稿时长
21 weeks
期刊介绍: BMC Palliative Care is an open access journal publishing original peer-reviewed research articles in the clinical, scientific, ethical and policy issues, local and international, regarding all aspects of hospice and palliative care for the dying and for those with profound suffering related to chronic illness.
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