| Literature DB >> 26097784 |
Abstract
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.Entities:
Keywords: dialysis; end-stage kidney disease; incidence; prevalence; registry
Year: 2015 PMID: 26097784 PMCID: PMC4455186 DOI: 10.1038/kisup.2015.8
Source DB: PubMed Journal: Kidney Int Suppl (2011) ISSN: 2157-1716