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加拿大原住民在器官移植过程中遭遇系统性种族主义的经验证据。

Experiential Evidence of Systemic Racism for Indigenous Peoples Navigating Transplantation in Canada.

作者信息

Kennedy Simone, Wiebe Robyn, Kaur Reetinder, Sasaki Ayumi, Charlie Adrienne, Assu Alissa, Jaure Allison, Gill Jagbir

机构信息

Kidney Transplant Research Program, Providence Research, Vancouver, British Columbia, Canada.

Sydney School of Public Health, University of Sydney, Sydney, New South Wales, Australia.

出版信息

Kidney Int Rep. 2025 Mar 6;10(5):1538-1547. doi: 10.1016/j.ekir.2025.02.027. eCollection 2025 May.

Abstract

INTRODUCTION

Despite previous data stating that Indigenous patients with kidney failure are 66% less likely to receive a kidney transplant compared with White Canadians, there is a very limited understanding of the barriers and challenges experienced and described by Indigenous Peoples when accessing kidney transplantation. The aim of this study was to describe the perspectives and experiences of Indigenous kidney transplant candidates and recipients, living kidney donors, and Elders on access to kidney transplantation in British Columbia, Canada in the hopes of codeveloping and implementing health services interventions to address systemic barriers to transplantation.

METHODS

Semistructured interviews were conducted with 19 participants and 4 focus groups were conducted with 18 participants ( = 37). Transcripts were thematically analyzed.

RESULTS

Five themes were identified as follows: (i) confronting uncertainty and risk, (ii) culture of giving, (iii) systemic racism and discrimination, (iv) navigating complexities of transplant and donation process, and (v) a lack of culturally safe care.

CONCLUSION

These findings highlight that Indigenous patients face potentially modifiable barriers that may be amenable to health system improvements, such as development of culturally safe patient education tools and Indigenous-specific navigation supports. Health services and policy interventions need to be explored and evaluated to begin to address inequities in access to transplantation.

摘要

引言

尽管此前有数据表明,与加拿大白人相比,患有肾衰竭的原住民患者接受肾移植的可能性要低66%,但对于原住民在获取肾移植时所经历和描述的障碍与挑战,人们的了解却非常有限。本研究的目的是描述加拿大不列颠哥伦比亚省原住民肾移植候选者、接受者、活体肾捐赠者以及长者在获取肾移植方面的观点和经历,以期共同制定并实施卫生服务干预措施,以消除移植过程中的系统性障碍。

方法

对19名参与者进行了半结构化访谈,并对18名参与者开展了4次焦点小组讨论(共37人)。对访谈记录进行了主题分析。

结果

确定了五个主题,分别为:(i)面对不确定性和风险;(ii)给予的文化;(iii)系统性种族主义和歧视;(iv)应对移植和捐赠过程的复杂性;(v)缺乏文化安全护理。

结论

这些研究结果表明,原住民患者面临一些可能通过改善卫生系统来消除的潜在障碍,例如开发具有文化安全性的患者教育工具以及针对原住民的导航支持。需要探索和评估卫生服务及政策干预措施,以着手解决移植获取方面的不平等问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e76e/12142638/5e9aa845a5fd/ga1.jpg

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