“ANZDATA” is the Australia and New Zealand Dialysis and Transplant Registry. ANZDATA collects information (data) about the treatment of all people (adults and children) in Australia and New Zealand who have kidney failure and have either dialysis or a kidney transplant.
Collecting information about the health and treatment of kidney patients helps hospitals make sure dialysis and transplantation is as safe as possible, helps hospitals and health services plan for services and to learn new things that may help you or others with kidney failure in the future.
Every year, hospitals and dialysis facilities complete a survey about patients’ health and kidney failure treatment and sends this information to ANZDATA either by computer or by post.
ANZDATA is paid for by the Australian and New Zealand Governments, Kidney Health Australia and the Australia and New Zealand Society of Nephrology, and has one office that is located in Adelaide.
Find out more at our website www.anzdata.org.au
Publications based upon ANZDATA Registry information reported or supplied upon request, must include the citation below and the following notice.
“The data reported here have been supplied by the Australia and New Zealand Dialysis and Transplant Registry. The interpretation and reporting of these data are the responsibility of the authors and in no way should be seen as an official policy or interpretation of the Australia and New Zealand Dialysis and Transplant Registry.”
ANZDATA Registry. 41st Report, Chapter 5: Peritoneal Dialysis, Australia and New Zealand Dialysis and Transplant Registry, Adelaide, Australia. 2018.
Available at: https://www.anzdata.org.au
Data requests are received and considered by the ANZDATA Executive following principles agreed by the Registry Advisory Committee (see Policy 2.2). There is a standard procedure for processing data requests received and releasing data to third parties. This can be found on our website at https://www.anzdata.org.au/anzdata/PoliciesProcedures/2.3Data_request_procedure_v2019.1.pdf