Profiles and outcomes of indigenous patients with chronic kidney disease in renal speciality clinics in the public health system in Queensland, Australia

Abstract Background High rates of chronic kidney disease (CKD) are well recognised in Australia’s Indigenous people, but kidney replacement therapy (KRT) registrations give an incomplete view of disease burden and outcomes. We describe profiles and outcomes of Indigenous people with preterminal CKD...

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Detalhes bibliográficos

Principais autores:	Wendy E. Hoy, Vishal Diwan, Zaimin Wang, Jenny Zhang, Anne Cameron, Sree K. Venuthurupalli, Robert G. Fassett, Samuel Chan, Helen G. Healy, Ken-Soon Tan, Richard Baer, Andrew J. Mallett, Nicholas Gray, Murty Mantha, Roy Cherian, Clyson Mutatiri, Krishan Madhan, George Kan, Geoffrey Mitchell, Shahadat Hossain, Danielle Wu, Thin Han, Adrian Kark, Sonia Coleman, Thomas Titus, Dwarakanatan Ranganathan, Ann Bonner, Sridevi Govindarajulu, Claire Brolan, Adithya Sreedharan, Tracey Johnson, Suzanne Williams
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2026-03-01
coleção:	BMC Nephrology
Assuntos:	Chronic kidney disease CKD burden CKD monitoring CKD QLD registry Indigenous australians
Acesso em linha:	https://doi.org/10.1186/s12882-026-04878-1
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