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Understanding Chinese-Canadian pathways to a diagnosis of dementia through a critical-constructionist lens

机译:通过批判建构主义的视角了解中加拿大诊断痴呆的途径

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Efforts to understand pathways to a diagnosis of Alzheimer's Disease and Related Dementias (ADRD) are important in light of the benefits of early diagnosis to both patients and families, but very little is known about the ways in which persons with dementia and their family caregivers experience this pathway from the point of initial symptom recognition by family or friends to formal diagnosis seeking, particularly for immigrant older adults. Our team employed qualitative methods and a critical constructionist and intersectional framework to understand this experience from the perspectives often Chinese-Canadian dyads of persons with dementia and their caregivers. Situating the decisions made by these dyads relative to their intersecting identities and the power structures that inhibit them steered us away from essentializing attributions of their experiences to their 'culture' or ethnicity. Early signs of dementia were recognized as such in hindsight. There was no evidence of a strong link between culture and symptom appraisal. Knowledge about dementia, which may be influenced by culture, age, income, knowledge of English, and other determinants of health, played a role in symptom appraisal and help seeking. The role of family caregivers in care-seeking was more highly influenced by structural factors than by traditional Chinese cultural norms about family responsibilities and filial piety. Once caregivers realized that the symptoms and behaviors were 'problematic,' they quickly sought out additional information, usually from a family physician. At 1.5 years, the time between symptom onset and diagnosis is comparable to or shorter than that reported in research with other cultural groups. Gender-based power imbalance between female family caregivers and male Chinese-Canadian physicians appear to have contributed to delayed investigations and diagnosis. Sensitivity to such imbalances is important when working with older adults and those from more hierarchical cul...
机译:鉴于尽早诊断对患者和家属都有好处,因此努力了解阿尔茨海默氏病和相关痴呆症的诊断途径非常重要,但对于痴呆症患者及其家庭护理人员的体验方式知之甚少从家人或朋友最初的症状识别到正式诊断的过程,尤其是对于移民的老年人。我们的团队采用定性方法,严格的建构主义和交叉框架来从华裔加拿大痴呆症患者及其照护者的双胞胎视角理解这一经验。将这些二元论相对于他们的相交身份和阻碍他们发展的权力结构所做出的决定放在首位,这使我们无法将他们的经验归因于他们的“文化”或种族。事后看来,痴呆的早期迹象已被确认。没有证据表明文化和症状评估之间有很强的联系。有关痴呆症的知识可能会受到文化,年龄,收入,英语知识以及其他健康决定因素的影响,在症状评估和寻求帮助中发挥作用。家庭看护人在寻求照顾中的作用受结构因素的影响要比受中国传统的有关家庭责任和孝道的文化规范影响更大。一旦看护者意识到症状和行为“有问题”,他们通常会从家庭医生那里迅速寻求更多信息。在1.5岁时,症状发作和诊断之间的时间与其他文化群体的研究报告的时间相当或更短。女性家庭照料者与男性加拿大华裔医生之间基于性别的权力失衡似乎加剧了调查和诊断的延迟。当与老年人以及来自更分层文化的人一起工作时,对这种失衡的敏感性非常重要。

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