Care and decision-making at the end of life for migrants living in the Netherlands: An intersectional analysis

IF 3.9 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Marieke Torensma , Xanthe de Voogd , Roukayya Oueslati , Irene G.M. van Valkengoed , Dick L. Willems , Bregje D. Onwuteaka-Philipsen , Jeanine L. Suurmond
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Abstract

As migrant populations age, the care system is confronted with the question how to respond to care needs of an increasingly diverse population of older adults. We used qualitative intersectional analysis to examine differential preferences and experiences with care at the end of life of twenty-five patients and their relatives from Suriname, Morocco and Turkey living in The Netherlands. Our analysis focused on the question how – in light of impairment – ethnicity, religion and gender intersect to create differences in social position that shape preferences and experiences related to three main themes: place of care at the end of life; discussing prognosis, advance care, and end-of-life care; and, end-of-life decision-making.
Our findings show that belonging to an ethnic or religious minority brings forth concerns about responsive care. In the nursing home, patients’ minority position and the interplay thereof with gender make it difficult for female patients to request and receive responsive care. Patients with a strong religious affiliation prefer to discuss diagnosis but not prognosis. These preferences are at interplay with factors related to socioeconomic status. The oversight of this variance hampers responsive care for patients and relatives. Preferences for discussion of medical aspects of care are subject to functional impairment and faith. Personal values and goals often remain unexpressed. Lastly, preferences regarding medical end-of-life decisions are foremost subject to religious affiliation and associated moral values. Respondents’ impairment and limited Dutch language proficiency requires their children to be involved in decision-making. Intersecting gendered care roles determine that mostly daughters are involved.
Considering the interplay of aspects of social identity and their effect on social positioning, and pro-active enquiry into values, goals and preferences for end-of-life care of patients and their relatives are paramount to achieve person centred and family-oriented care responsive to the needs of diverse communities.
生活在荷兰的移民临终关怀和决策:交叉分析。
随着流动人口的老龄化,护理系统面临着如何应对日益多样化的老年人的护理需求的问题。我们使用定性交叉分析来检查25名来自苏里南、摩洛哥和土耳其的患者及其亲属在荷兰生活的临终关怀的不同偏好和经历。我们的分析集中在种族、宗教和性别如何在残疾的情况下产生社会地位的差异,这些差异影响了与三个主题相关的偏好和经历:临终关怀的地点;讨论预后、预先护理和临终关怀;还有,临终决策。我们的研究结果表明,属于少数民族或宗教少数派会引起对反应性护理的关注。在养老院中,患者的少数民族地位及其与性别的相互作用使得女性患者难以要求和接受响应性护理。有强烈宗教信仰的患者更愿意讨论诊断而不是预后。这些偏好与社会经济地位相关的因素相互作用。对这种差异的监督阻碍了对患者和家属的响应性护理。对医疗方面的讨论的偏好取决于功能障碍和信仰。个人价值观和目标往往没有表达出来。最后,关于临终医疗决定的偏好主要取决于宗教信仰和相关的道德价值观。受访者的荷兰语能力受损和有限,要求他们的孩子参与决策。交叉的性别照顾角色决定了大多数女儿都参与其中。考虑到社会认同的相互作用及其对社会定位的影响,以及对患者及其亲属的临终关怀的价值观、目标和偏好的积极调查,对于实现以人为本和面向家庭的护理是至关重要的,以满足不同社区的需求。
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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来源期刊
Journal of Migration and Health
Journal of Migration and Health Social Sciences-Sociology and Political Science
CiteScore
5.70
自引率
8.70%
发文量
65
审稿时长
153 days
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