Suppr超能文献

记忆的低语:尼日利亚家庭如何在生物医学视角之外寻求痴呆症支持

Whispers of memory: How families navigate dementia support beyond the biomedical lens in Nigeria.

作者信息

Oyinlola Oluwagbemiga, Sussman Tamara, Mfoafo-M'Carthy Magnus, Adebusoye Lawrence Adekunle

机构信息

School of Social Work, McGill University, Montreal, Quebec, Canada.

Lyle S. Hallman Faculty of Social Work, Wilfrid Laurier University, Kitchener, Ontario, Canada.

出版信息

Alzheimers Dement. 2025 Jul;21(7):e70290. doi: 10.1002/alz.70290.

Abstract

INTRODUCTION

Research on dementia caregiving in Africa often prioritizes biomedical and formal health-care services, overlooking broader family and community-based support networks. Addressing this gap, this study explores when and which support services Yoruba families use and how these services shape their caregiving experiences within the dementia care context.

METHODS

Guided by interpretive phenomenology and Afrocentric principles, we conducted 15 semi-structured family interviews with 52 participants (2-5 per family), alongside persons with dementia. Interviews were audio-recorded, translated, and thematically analyzed.

RESULTS

Help seeking often began when behavioral symptoms became overwhelming. Urban families (n = 11) leaned on hospital services, while rural families (n = 4) turned to faith-based and traditional healers. Support was appreciated for offering reassurance, though hospital services often lacked cultural sensitivity, and traditional options-while fostering hope-could reinforce stigma.

DISCUSSION

Enhancing dementia awareness and collaboration between medical, spiritual, and traditional systems may improve caregiver experiences and encourage earlier, culturally appropriate interventions.

HIGHLIGHTS

Yoruba families caring for loved ones with dementia do not adhere to rigid care pathways. Instead, they move fluidly between hospitals, religious spaces, and traditional healing practices-not just in search of treatment but to find meaning, reassurance, and continuity with ancestral ways of knowing. Memory loss is not always seen as a medical condition; it is often interpreted through spiritual, cultural, and communal lenses. Families may turn to faith leaders or elders first, delaying formal care until behaviors become disruptive or socially visible. Our interpretive phenomenological analysis, grounded in an Afrocentric lens, reveals caregiving as both an expression of love and a weighty responsibility. The ever-present fear of judgment-from within and outside the family-can lead to silence, isolation, and hesitation in seeking biomedical support. A more compassionate and culturally anchored dementia care model requires health-care professionals, traditional healers, and faith leaders to work together. Through dialogue and mutual respect, they can create care networks that honor Yoruba worldviews, allowing families to navigate dementia in ways that feel both medically sound and spiritually resonant.

摘要

引言

非洲关于痴呆症护理的研究通常将生物医学和正规医疗服务作为重点,而忽视了更广泛的家庭和社区支持网络。为了填补这一空白,本研究探讨约鲁巴家庭在何时以及使用哪些支持服务,以及这些服务如何在痴呆症护理背景下塑造他们的护理体验。

方法

在解释现象学和以非洲为中心的原则指导下,我们对52名参与者(每个家庭2 - 5人)以及痴呆症患者进行了15次半结构化家庭访谈。访谈进行了录音、翻译并进行了主题分析。

结果

当行为症状变得无法承受时,通常就会开始寻求帮助。城市家庭(n = 11)依赖医院服务,而农村家庭(n = 4)则求助于宗教人士和传统治疗师。人们对所提供的支持表示感激,因为它能让人安心,不过医院服务往往缺乏文化敏感性,而传统选择虽然能带来希望,但可能会强化污名化。

讨论

提高对痴呆症的认识以及加强医疗、精神和传统体系之间的合作,可能会改善护理人员的体验,并鼓励更早地采取符合文化的干预措施。

要点

照顾患有痴呆症亲人的约鲁巴家庭并不遵循固定的护理路径。相反,他们在医院、宗教场所和传统治疗方式之间灵活转换,这不仅是为了寻求治疗,也是为了寻找意义、安心,并与祖先的认知方式保持连续性。记忆丧失并不总是被视为一种医学状况;它通常通过精神、文化和社区的视角来解读。家庭可能首先求助于宗教领袖或长辈,直到行为变得具有破坏性或在社会上引起关注才会延迟寻求正规护理。我们基于以非洲为中心视角的解释现象学分析表明,护理既是爱的表达,也是一项重大责任。来自家庭内部和外部的对评判的持续恐惧,可能导致在寻求生物医学支持时保持沉默、孤立和犹豫。一个更具同情心和文化根基的痴呆症护理模式需要医疗保健专业人员、传统治疗师和宗教领袖共同努力。通过对话和相互尊重,他们可以创建尊重约鲁巴世界观的护理网络,让家庭能够以在医学上合理且在精神上共鸣的方式应对痴呆症。

相似文献

本文引用的文献

10
Perceptions and experiences of dementia and its care in rural Kenya.肯尼亚农村地区对痴呆症及其护理的认知和体验。
Dementia (London). 2021 Nov;20(8):2802-2819. doi: 10.1177/14713012211014800. Epub 2021 Apr 30.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验