Perspectives of elders and their adult children of Black and minority ethnic heritage on end-of-life conversations: A meta-ethnography

奇纳 民族 心理信息 包裹体(矿物) 批判性评价 临终关怀 民族志 生活质量(医疗保健) 缓和医疗 梅德林 老年学 医学 引用 心理学 护理部 社会学 社会心理学 图书馆学 替代医学 心理干预 政治学 人类学 病理 计算机科学 法学
作者
Joanna De Souza,Karen Gillett,Katherine Froggatt,Catherine Walshe
出处
期刊:Palliative Medicine [SAGE Publishing]
卷期号:34 (2): 195-208 被引量:22
标识
DOI:10.1177/0269216319887070
摘要

Background: People of Black and minority ethnic heritage are more likely to die receiving life supporting measures and less likely to die at home. End-of-life care decision making often involves adult children as advance care planning is uncommon in these communities. Physicians report family distress as being a major factor in continuing with futile care. Aim: To develop a deeper understanding of the perspectives of elders of Black and minority ethnic heritage and their children, about end-of-life conversations that take place within the family, using a meta-ethnographic approach Design: Systematic interpretive exploration using the process of meta-ethnography was utilised. Data sources: CINAHL, MEDLINE, PubMed and PsycINFO databases were searched. Inclusion criteria included studies published between 2005 and 2019 and studies of conversations between ethnic minority elders and family about end-of-life care. Citation snowballing was used to ensure all appropriate references were identified. A total of 13 studies met the inclusion criteria and required quality level using Critical Appraisal Skills Programme. Results: The following four storylines were constructed: ‘My family will carry out everything for me; it is trust’; ‘No Mum, don’t talk like that’; ‘I leave it in God’s hands’; and ‘Who’s going to look after us?’ The synthesis reflected the dichotomous balance of trust and burden avoidance that characterises the perspectives of Black and minority ethnic elders to end-of-life care planning with their children.

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