Australia and New Zealand dialysis and transplant registry

Research output: Contribution to journalArticle

14 Citations (Scopus)


The ANZDATA Registry includes all patients treated with renal replacement therapy (RRT) throughout Australia and New Zealand. Funding is predominantly from government sources, together with the non-government organization Kidney Health Australia. Registry operations are overseen by an Executive committee, and a Steering Committee with wide representation. Data is collected from renal units throughout Australia and New Zealand on a regular basis, and forwarded to the Registry. Areas covered include demographic details, primary renal disease, type of renal replacement therapy, process measures, and a variety of outcomes. From this data collection a number of themes of work are produced. These include production of Registry reports with an extensive range of national and regional data, a suite of quality assurance reports, key process indicator (KPI) reports, and data sets for a variety of audit and research purposes. The various types of information from the ANZDATA Registry are used in a wide variety of areas, including health services planning, safety and quality programs, and clinical research projects.

Original languageEnglish
Pages (from-to)39-44
Number of pages6
JournalKidney International Supplements
Issue number1
Publication statusPublished - 1 Jun 2015


  • dialysis
  • end-stage kidney disease
  • incidence
  • prevalence
  • registry

ASJC Scopus subject areas

  • Nephrology

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