Reports and research
Reports and research using UK Renal Registry (UKRR) and National Registry of Rare Kidney Diseases (RaDaR) data build our understanding of kidney disease, treatment and outcomes.
Our national clinical audit reports help kidney teams assess care against clinical standards, understand variation and identify priorities for improvement. Research publications explore these findings further, contributing evidence to inform clinical practice and future research.
National and centre-level analyses of care and outcomes for adults and children with CKD, including people receiving dialysis or living with a kidney transplant.
Reports on AKI in England, examining patterns in laboratory alerts, the populations affected and patient outcomes.
Findings from the National Kidney Patient Survey, previously known as the Kidney PREM. These reports examine patients’ experiences of kidney care and identify opportunities for services to improve.
Our disparities reports examine differences in care and outcomes associated with age, sex, ethnicity and socioeconomic circumstances among people with kidney failure.
Other reports and research
Using and acknowledging our work
If you are producing a publication or presentation using UKRR data, include the appropriate acknowledgement and disclaimer.