Early identification of CKD and risk of dialysis

  • Research type

    Research Database

  • IRAS ID

    306012

  • Contact name

    Spiros Denaxas

  • Contact email

    s.denaxas@ucl.ac.uk

  • Research summary

    National Chronic Kidney Disease Audit (linked to UK Renal Registry, Hospital Episode Statistics, National Institute of Cardiovascular Outcomes Research))

  • REC name

    London - Chelsea Research Ethics Committee

  • REC reference

    22/LO/0222

  • Date of REC Opinion

    12 Apr 2022

  • REC opinion

    Favourable Opinion

  • Data collection arrangements

    The National Chronic Kidney Disease Audit (NCKDA) collected between 2014-2016 data from 1057 general practices in England and Wales on testing of patients at risk of chronic kidney disease, as well as the identification and management of patients with chronic kidney disease. The current application is to continue to allow the data to be used in future research of long term outcomes of Audit participants.

    Anonymised clinical data will be stored at the London School of Hygiene & Tropical Medicine. Identifiable data (e.g. NHS numbers) will be stored separately in the secure data haven at the University College London.

    Future data on the outcomes (e.g. hospitalisations, deaths, heart disease, acute kidney problems in the context of other illness, complete kidney failure with need of dialysis) of patients who provided data for the audit will be collected by linking the NHS numbers to clinical records held in other databases, thus forming a large cohort study on outcomes and health needs of patients at risk of or with chronic kidney disease in primary care.

  • Research programme

    If this application was approved, data from the National Chronic Kidney Disease Audit with its follow-up of health outcomes will continue to provide a very large cohort study of kidney disease. The availability of additional information on those with advanced kidney disease held in the UK Renal Association Renal Registry would enable research across the entire patient journey from primary to secondary and then tertiary care. Many patients with kidney disease develop cardiovascular problems, and the present application would enable linkage to hospital records as well as to data on heart failure and heart attacks which are held at the National Institute for Cardiovascular Outcomes Research. Thus the proposed database would benefit both the renal and cardiovascular research community and continue to provide important information that would help improve the clinical services for patients at risk of or with kidney disease.

  • Research database title

    National Chronic Kidney Disease Audit (linked to UK Renal Registry, Hospital Episode Statistics, National Institute of Cardiovascular Outcomes Research))

  • Establishment organisation

    UCL Information Services Division

  • Establishment organisation address

    University College London, Gower Street

    NW1 2DA