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Experiences of racism related to kidney transplantation in Aotearoa New Zealand

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Summary:

Racism may be contributing to kidney transplantation inequity in New Zealand, according to a study of 40 Māori with kidney disease, their family members and donors. Semi-structured interviews were conducted between September and December 2020, and participants included those with kidney disease who had considered, were being worked up for, or who had already received a kidney transplant as well as family members and potential or previous donors. Subthemes were identified at each level of racism: institutional (excluded and devalued by health system; disease stigmatisation; discriminatory body weight criteria, lack of power), personally mediated (experiencing racial profiling; explicit racism), and internalised racism (shame and unworthiness to receive a transplant). Addressing racism at all levels is imperative if inequitable outcomes for Māori requiring kidney transplantation are to be addressed, the study authors concluded.

Comment:
Reading this made me think of Vera Keefe, at the Eru Pōmare Centre, who, back in the 1990s, alerted us to the racism she experienced in her own transplant journey. I hope that this evidence brings much needed, and long-awaited, change.
Reference: J Racial Ethn Health Disparities. 2023; 10(1):219-227.
Independent commentary by Dr. Matire Hardwood

Dr Matire Harwood (Ngapuhi) has worked in Hauora Māori, primary health and rehabilitation settings as clinician and researcher since graduating from Auckland Medical School in 1994. She also holds positions on a number of boards, committees and advisory groups including the Health Research Council. Matire lives in Auckland with her whānau including partner Haunui and two young children Te Rangiura and Waimarie.

Research Review publications are intended for New Zealand health professionals.

Disclaimer: This publication is not intended as a replacement for regular medical education but to assist in the process. The reviews are a summarised interpretation of the published study and reflect the opinion of the writer rather than those of the research group or scientific journal. It is suggested readers review the full trial data before forming a final conclusion on its merits.

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