Ajmera Transplant Centre, University Health Network, Toronto, Ontario, Canada.
Black Health Alliance, Toronto, Ontario, Canada.
BMJ Open. 2023 Aug 16;13(8):e073176. doi: 10.1136/bmjopen-2023-073176.
Living donor (LD) kidney transplant (KT) is the best treatment option for many patients with kidney failure as it improves quality of life and survival compared with dialysis and deceased donor KT. Unfortunately, LDKT is underused, especially among groups marginalised by race and ethnicity. African, Caribbean and Black (ACB) patients are 60%-70% less likely to receive LDKT in Canada compared with white patients. Research from the USA and the UK suggests that mistrust, cultural and generational norms, access, and affordability may contribute to inequities. To date, no Canadian studies have explored the beliefs and behaviours related to LDKT in ACB communities. Research approaches that use a critical, community-based approach can help illuminate broader structural factors that may shape individual beliefs and behaviours. In this qualitative study, we will investigate barriers to accessing LDKT in ACB communities in the Greater Toronto Area, to enhance our understanding of the perspectives and experiences of ACB community members, both with and without lived experience of chronic kidney disease (CKD).
Hospital-based and community-based recruitment strategies will be used to recruit participants for focus groups and individual interviews. Participants will include self-identified ACB individuals with and without experiences of CKD and nephrology professionals. Collaboration with ACB community partners will facilitate a community-based research approach. Data will be analysed using reflexive thematic analysis and critical race theory. Findings will be revised based on feedback from ACB community partners.
This study has been approved by the University Health Network Research Ethics Board UHN REB file #15-9775. Study findings will contribute to the codevelopment of culturally safe and responsive educational materials to raise awareness about CKD and its treatments and to improve equitable access to high-quality kidney care, including LDKT, for ACB patients.
对于许多肾衰竭患者来说,活体供者(LD)肾脏移植(KT)是最佳的治疗选择,因为与透析和已故供者 KT 相比,它可以提高生活质量和生存率。不幸的是,LDKT 的使用率较低,尤其是在因种族和民族而处于劣势的群体中。与白人患者相比,加拿大的非洲裔、加勒比裔和黑人(ACB)患者接受 LDKT 的可能性低 60%-70%。来自美国和英国的研究表明,不信任、文化和代际规范、获取途径和负担能力可能导致不平等。迄今为止,加拿大尚无研究探讨过 ACB 社区中与 LDKT 相关的信仰和行为。使用批判性、以社区为基础的研究方法可以帮助阐明可能影响个人信仰和行为的更广泛的结构性因素。在这项定性研究中,我们将调查在大多伦多地区的 ACB 社区中获取 LDKT 的障碍,以增强我们对 ACB 社区成员的观点和经验的理解,包括有和没有慢性肾病(CKD)经历的成员。
将采用基于医院和社区的招募策略招募参与者参加焦点小组和个人访谈。参与者将包括自我认同的具有和不具有 CKD 经历的 ACB 个体以及肾脏病学专业人员。与 ACB 社区合作伙伴的合作将促进基于社区的研究方法。将使用反思性主题分析和批判种族理论分析数据。将根据 ACB 社区合作伙伴的反馈意见修订研究结果。
本研究已获得多伦多大学健康网络伦理审查委员会 UHN REB 文件 #15-9775 的批准。研究结果将有助于共同制定文化安全和响应式教育材料,提高对 CKD 及其治疗方法的认识,并改善公平获得高质量肾脏护理的机会,包括 ACB 患者的 LDKT。