The spotlight is on the kidney health of Aboriginal and Torres Strait Islander peoples, with a new supplement published today in the Medical Journal of Australia.
The supplement highlights the need for equity for Aboriginal and Torres Strait Islander people who require a kidney transplant and demonstrates the importance of engaging with Indigenous communities about their health and wellbeing needs.
“Recorded rates of kidney failure requiring dialysis or transplantation among Aboriginal and Torres Strait Islander Australians have risen progressively over the past 40 years, remaining consistently higher than rates for non-Indigenous Australians,” wrote the authors, including Professor Jaquelyne Hughes, a clinical research professor at Flinders University and a consultant nephrologist.
“Aboriginal and Torres Strait Islander people have age-adjusted incidence rates of kidney replacement therapy — dialysis or transplantation — eight to nine times higher than those of non-Indigenous Australians, with the median age of Aboriginal and Torres Strait Islander people who experience kidney failure being nearly 30 years younger than non-Indigenous people.”
In light of this information and community and clinician prioritising, a 23-member National Indigenous Kidney Transplantation Taskforce (NIKTT) was commissioned in 2019. It has worked to improve access to the kidney transplant waiting list for Aboriginal and Torres Strait Islander peoples.
“The taskforce looked within ANZDATA to learn about presenting a data pathway of clients and clinicians working together through the transplant assessments,” Professor Stephen McDonald, Chair of NIKTT, said.
“Taskforce members also said they needed local support to improve the local pathway, and NIKTT supported seven local projects with a one-year equity and access sponsorship.”
The NIKKT was tasked with reporting on the extent of effort to reduce cultural bias in the kidney transplant area. It worked with the Lowitja Institute, which produced a cultural bias report that identified a dearth of publications. This highlights how future health improvements in kidney transplantation should be designed and also publicly reports on cultural bias and the steps taken by the NIKKT to mitigate cultural bias influencing access to transplantation.
It was therefore crucial to establish a national network of Indigenous Reference Groups; this was led by supplement co-author Kelli Owen, the national community engagement coordinator for the NKTT.
“Although there have been so many efforts to improve kidney health outcomes for Aboriginal and Torres Strait Islander people, there has not been a coordinated approach to consultation on addressing these challenges or improving service delivery,” Ms Owen said.
“The key focus of the Taskforce is embedding our people’s self-determination and authority into designing models of care to improve access to kidney transplantation.
“Before the establishment of the Indigenous Reference Groups, there was very limited input by Aboriginal and Torres Strait Islander consumers into the processes of care in renal units and no input about care in kidney transplant units.”
Health systems across Australia need to be empowered to embrace and work with Indigenous knowledges, the authors wrote.
“For Aboriginal and Torres Strait Islander peoples living with kidney disease and after transplantation, the health system must embed true partnership, engagement and, most importantly, real change from existing verbal feedback that is backed by evidence,” Ms Owen said.
The MJA’s cover page today also features a photo of message sticks.
“The message sticks depicted on the cover of the MJA today were purchased for our Indigenous Reference Groups,” Ms Owen said.
“The message sticks help keep formalities at a meeting, with only the person holding a stick being able to have the floor.”
Professor Hughes said the message sticks and the MJA cover were a visible demonstration of the way the taskforce and communities and listening to each other and working collaboratively.
“The taskforce was a fantastic opportunity for Aboriginal and Torres Strait Islander peoples to create change they needed in health care, with the Indigenous Reference Groups carrying the voice and message of our people back to the taskforce and onwards to Canberra,” Professor Hughes said.
“We look forward to a commitment for continued support of the Taskforce, so that we can be sure that improved kidney health and wellbeing among all our people is seen in real improvements in peoples lives and captured in routine data reporting.”
Read the research in the Medical Journal of Australia.
The Medical Journal of Australia is a publication of the Australian Medical Association.
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- Sam Hunt