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共同应对 COVID-19 大流行:早期痴呆症患者及其成年子女之间的讨论。

Navigating the COVID-19 pandemic together: Discussions between persons with early-stage dementia and their adult children.

机构信息

Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut, USA.

Yale College, New Haven, Connecticut, USA.

出版信息

Int J Geriatr Psychiatry. 2023 Mar;38(3):e5905. doi: 10.1002/gps.5905.

Abstract

OBJECTIVES

Studies have separately examined the health impacts of the COVID-19 pandemic on persons with dementia and their caregivers. Less attention has been paid to the social and emotional impacts of the pandemic in this population or how these individuals are mutually coping with the pandemic. Guided by the social citizenship theory, this qualitative study sought to characterize how persons with dementia and their adult children are coping during this time with a focus on the strengths demonstrated by persons with dementia.

METHODS

Participants were 43 dyads of individuals aged 55 and older with early-stage dementia and their adult children. Discussions between parent-child dyads were recorded. Using reflexive thematic analysis, themes related to social and emotional impacts of the pandemic and coping strategies were identified.

RESULTS

Adult children shared with their parents how the pandemic resulted in reduced social engagement and challenging work arrangements. Dyads described how the pandemic positively impacted their relationship, allowing some of them to spend more time together. In coping with the pandemic, adult children provided instrumental support to their parents and parents reciprocated with emotional support. Participants also coped by making meaning of their situation during discussions.

CONCLUSIONS

Findings characterize the resilience of persons with dementia and the mutuality of the relationship between both members of the care partner dyad, as both parents and adult children offered support to one another. Facilitating dyadic discussions may be a cost-effective way to sustain social connections and offer ongoing coping support through the pandemic or other challenging circumstances.

摘要

目的

已有研究分别考察了 COVID-19 大流行对痴呆症患者及其照护者的健康影响。但较少关注该人群中大流行的社会和情感影响,也较少关注这些人如何相互应对大流行。本研究以社会公民理论为指导,旨在描述痴呆症患者及其成年子女在此期间的应对方式,重点关注痴呆症患者表现出的优势。

方法

参与者为 43 对年龄在 55 岁及以上、患有早期痴呆症的个体及其成年子女。记录了父母-子女对子之间的讨论。采用反思性主题分析,确定了与大流行的社会和情感影响以及应对策略相关的主题。

结果

成年子女与父母分享了大流行如何导致社交活动减少和工作安排具有挑战性。对子描述了大流行如何对他们的关系产生积极影响,使他们中的一些人能够有更多的时间在一起。在应对大流行时,成年子女为父母提供了工具性支持,而父母则以情感支持作为回报。参与者还通过在讨论中对自己的情况进行意义建构来应对。

结论

研究结果描述了痴呆症患者的适应能力,以及照护伙伴对子中两个成员之间关系的相互性,因为父母和成年子女都相互提供支持。促进对子讨论可能是一种具有成本效益的方式,可以通过大流行或其他具有挑战性的情况维持社交联系并提供持续的应对支持。

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