Department of Primary Care and Public Health Sciences, King's College London, London, UK.
Ethn Health. 2013;18(4):367-90. doi: 10.1080/13557858.2012.752073. Epub 2012 Dec 19.
A systematic review and synthesis of quantitative and qualitative research were undertaken to examine attitudes to deceased donation and registration as an organ donor among ethnic minorities in the U.K. and North America.
A systematic search and assessments of relevance and quality were conducted. Parallel syntheses were then undertaken of 14 quantitative and 12 qualitative papers followed by their integration. The synthesis was organised around five barriers that emerged as key issues: (1) knowledge regarding deceased donation and registration as a donor; (2) discussion of donation/registration with family members; (3) faith and cultural beliefs; (4) bodily concerns including disfigurement and intactness; and (5) trust in doctors and the health care system.
In all countries, knowledge of organ donation and registration remained low despite public campaigns, with African-Americans and Black African and Black Caribbean populations in the U.K. often regarding organ donation as a 'white' issue. Each of the four attitudinal barriers was also more prevalent among ethnic minorities compared with the majority population. However, the significance of trust and uncertainties regarding religion/faith differed between groups, reflecting salient aspects of ethnic identity and experiences. Differences were also identified within ethnic groups associated with age and generation, although respect for the views of elders often influenced younger peoples' willingness to donate.
There is a need for a more nuanced understanding of ethnicity and of variations in attitudes associated with country of origin, age/generation, socio-economic status and area of residence, to inform public campaigns and promote sensitive discussions with bereaved ethnic minority families. The traditional focus on knowledge and attitudes also requires to be complemented by a greater emphasis on organisational and service-related barriers and changes required to enhance ethnic minorities' access to registration as a donor and consent to deceased donation.
系统综述和综合定量和定性研究,以检查英国和北美的少数民族对已故捐赠者和器官捐献登记的态度。
进行了系统搜索,并对相关性和质量进行了评估。然后对 14 篇定量论文和 12 篇定性论文进行了平行综合,然后进行了整合。综合分析围绕着五个关键问题展开:(1)对已故捐赠和登记为捐赠者的知识;(2)与家人讨论捐赠/登记;(3)信仰和文化信仰;(4)身体问题,包括毁容和完整性;(5)对医生和医疗保健系统的信任。
在所有国家,尽管开展了公共宣传活动,但对器官捐赠和登记的了解仍然很低,英国的非裔美国人和非洲裔加勒比海人和黑人往往将器官捐赠视为“白人”问题。与多数人群相比,所有四个态度障碍在少数民族中更为普遍。然而,在信任和对宗教/信仰的不确定性方面,不同群体之间存在差异,这反映了种族身份和经历的显著方面。还在与年龄和代际相关的族裔群体中发现了差异,尽管尊重长辈的观点往往影响年轻人捐赠的意愿。
需要更细致地了解族裔群体以及与原籍国、年龄/代际、社会经济地位和居住地相关的态度差异,为宣传活动提供信息,并促进与少数民族悲痛欲绝的家庭进行敏感讨论。传统上对知识和态度的关注也需要辅以更加强调组织和服务相关障碍,以及为增强少数民族登记为捐赠者和同意已故捐赠而需要进行的变革。