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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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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: BMC 2026-03-01
Col·lecció:BMC Nephrology
Matèries:
Chronic kidney disease
CKD burden
CKD monitoring
CKD QLD registry
Indigenous australians
Accés en línia:https://doi.org/10.1186/s12882-026-04878-1
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