Ménard Alixe, Adekoya Adebusola, Birchall Elizabeth, Seetharaman Kishore, Kervin Lucy, Khan Koushambhi, Baumbusch Jennifer
Faculty of Health Sciences, Interdisciplinary School of Health Sciences, University of Ottawa, Ottawa, ON, Canada.
School of Public Health Sciences, University of Waterloo, Waterloo, ON, Canada.
BMC Med Ethics. 2025 Mar 21;26(1):39. doi: 10.1186/s12910-025-01197-2.
Future planning is essential for care partners to discuss and prepare for the goals of care for their relatives living with dementia. However, engaging in these discussions can be particularly challenging as care partners navigate the unpredictable and uncertain trajectory of dementia. This study aimed to explore how care partners of persons living with dementia engage in future planning (or not) throughout the dementia journey.
This multi-method qualitative study used a relational autonomy framework to examine the experiences of care partners providing daily care to a person living with dementia. Fifteen care partners from British Columbia, Canada, participated in semi-structured interviews and maintained reflective diaries over a period of up to two years (August 2020-October 2023). Data were analyzed using thematic analysis to identify patterns and themes related to future planning.
Four key themes were identified through the analysis: (1) changes to living arrangements, as care partners adjusted to the evolving needs of their relatives; (2) anticipatory grief, reflecting the emotional impact of witnessing the progression of dementia; (3) future planning with changing health, highlighting the challenges of aligning care plans with the shifting health status of the person living with dementia; and (4) finding hope, as care partners sought meaning and optimism amidst uncertainty.
This study underscores the complex and dynamic nature of future planning for care partners of individuals with progressive dementias. The findings highlight the need for tailored resources and interventions to support care partners in navigating future planning discussions, particularly in light of the emotional and relational challenges they face. Developing such resources could improve the preparedness and well-being of care partners as they engage in this critical aspect of caregiving.
对于护理伙伴来说,未来规划对于讨论并为患有痴呆症的亲属的护理目标做准备至关重要。然而,参与这些讨论可能极具挑战性,因为护理伙伴要应对痴呆症不可预测且不确定的病程。本研究旨在探讨痴呆症患者的护理伙伴在整个痴呆症病程中是如何(或未如何)参与未来规划的。
这项多方法定性研究使用关系自主性框架来考察为痴呆症患者提供日常护理的护理伙伴的经历。来自加拿大不列颠哥伦比亚省的15名护理伙伴参与了半结构化访谈,并在长达两年的时间里(2020年8月至2023年10月)撰写反思日记。使用主题分析法对数据进行分析,以识别与未来规划相关的模式和主题。
通过分析确定了四个关键主题:(1)生活安排的变化,即护理伙伴根据亲属不断变化的需求进行调整;(2)预期性悲伤,反映目睹痴呆症进展的情感影响;(3)随着健康状况变化进行未来规划,突出了使护理计划与痴呆症患者不断变化的健康状况相匹配的挑战;(4)寻找希望,即护理伙伴在不确定性中寻求意义和乐观。
本研究强调了为进行性痴呆症患者的护理伙伴进行未来规划的复杂性和动态性。研究结果凸显了需要有针对性的资源和干预措施,以支持护理伙伴参与未来规划讨论,特别是鉴于他们面临的情感和关系挑战。开发此类资源可以提高护理伙伴在参与这一关键护理环节时的准备程度和幸福感。