Caregiver Perspectives on Alzheimer's Care in the Turkish Sociocultural Context.

IF 2.2
Hatice Reyhan Özgöbek, Zeynep Güldem Ökem, İlknur Yüksel-Kaptanoğlu, Sıdıka Kaya
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Abstract

In the context of global demographic change, the number of patients with Alzheimer's disease (AD) and other forms of dementia is steadily increasing. These individuals require ongoing care but often struggle to communicate their needs and preferences regarding quality care. This study re-examines existing qualitative data to explore perceptions of "quality care" for patients with AD within the Turkish sociocultural context. Building on a primary study of caregivers' definitions of quality care, it employs a secondary analysis approach to generate new insights without collecting additional data. The dataset includes face-to-face, semi-structured interviews conducted in 2018 with 15 formal and informal caregivers, including family members, professional caregivers, and managers from care institutions across four provinces in Türkiye. Analysis reveals that patients with AD often experience discomfort when their bodies are exposed or touched, particularly in ways that infringe upon their sense of privacy. Caregivers emphasised that protecting privacy relies on understanding the individual's life story, values, and preferences, highlighting the role of relational familiarity in delivering care. Many participants described forming close, family-like bonds, often adopting kinship roles to provide personalised support. These dynamics were also shaped by gender norms, with caregiving commonly framed through a mother-child lens, reflecting societal expectations that women assume primary caregiving responsibilities. The findings show how privacy, emotional closeness, and gender roles intersect to shape caregiving practices. These findings suggest that care quality for patients with AD in Türkiye may be enhanced by approaches that attend to cultural and relational dimensions, recognise caregiver support needs, and incorporate culturally attuned practices - though further research across diverse settings is needed to assess the broader applicability of these insights. These insights contribute to the international discourse on dementia care by showing how culturally specific practices can guide globally relevant approaches to quality care.

土耳其社会文化背景下阿尔茨海默氏症护理者的观点。
在全球人口结构变化的背景下,阿尔茨海默病(AD)和其他形式的痴呆症患者数量正在稳步增加。这些人需要持续的护理,但往往难以沟通他们的需求和对优质护理的偏好。本研究重新检查了现有的定性数据,以探索在土耳其社会文化背景下对AD患者的“优质护理”的看法。在对护理人员对优质护理的定义进行初步研究的基础上,它采用了二次分析方法,在不收集额外数据的情况下产生新的见解。该数据集包括2018年对15名正式和非正式护理人员进行的面对面半结构化访谈,其中包括来自缅甸四个省的护理机构的家庭成员、专业护理人员和管理人员。分析显示,当他们的身体被暴露或触摸时,尤其是以侵犯他们隐私的方式接触时,阿尔茨海默病患者经常感到不适。护理人员强调,保护隐私依赖于了解个人的生活经历、价值观和偏好,强调了关系熟悉度在提供护理中的作用。许多参与者描述了建立亲密的家庭关系,通常采用亲属角色来提供个性化的支持。这些动态也受到性别规范的影响,照顾通常是通过母子视角来设定的,反映了社会对女性承担主要照顾责任的期望。研究结果表明,隐私、情感亲密和性别角色如何相互影响,影响着护理实践。这些发现表明,通过关注文化和关系维度的方法,认识到护理人员的支持需求,并纳入与文化相适应的做法,可以提高 rkiye AD患者的护理质量——尽管需要在不同环境中进行进一步的研究,以评估这些见解的更广泛的适用性。这些见解通过展示特定文化的实践如何指导全球相关的高质量护理方法,为痴呆症护理的国际讨论做出了贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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