Brighton ARC Study

  • Research type

    Research Study

  • Full title

    Augmented Renal Clearance: a prospective cohort study in emergency admissions to intensive care.

  • IRAS ID

    319953

  • Contact name

    Barbara Philips

  • Contact email

    b.philips@bsms.ac.uk

  • Sponsor organisation

    University Hospitals Sussex NHS Foundation Trust

  • Duration of Study in the UK

    0 years, 12 months, 0 days

  • Research summary

    This observational cohort study aims to look at a broad cohort of general intensive care patients, to gain an understanding of how often we should be expecting to see augmented renal clearance (ARC). This study will recruit patients from the adult Intensive Care Unit (ICU) in the Royal Sussex County Hospital, Brighton. Recruitment will not be restricted by age or reason for admission. To ensure data collection is manageable, patients will be recruited weekly, recruiting those admitted to ICU over the weekend. The exposure in this prospective cohort study is therefore ICU admission, with the outcome as ARC, defined as creatinine clearance >130ml/min/1.73m^2.

    Urinary and serum creatinine will be collected from indwelling lines, for up to 5 days from recruitment. The urinary creatinine levels will be used to measure creatinine clearance. Serum creatinine levels are used in 3 different equations to calculate estimated creatinine clearance: Cockcroft-Gault (CG), the Modification of Diet in Renal Disease 7 (MDRD 7), 2021 Chronic Kidney Disease Epidemiology Collaboration (CKD-Epi). The estimated and measured creatinine clearance will be compared to assess the accuracy of these equations.

    A recent publication produced an ARC prediction tool, giving the probability for a particular patient to develop ARC in the next 24 hours. The research team tested this on patients in Belgium, but it is unknown if this has external validity with a UK cohort, and therefore, if it has use in a UK-based hospital. An online version of this tool is available for research purposes and will be used to investigate the accuracy and precision of the tool when compared to confirmed incidence of ARC in this cohort of patients.

  • REC name

    Wales REC 1

  • REC reference

    24/WA/0080

  • Date of REC Opinion

    19 Jun 2024

  • REC opinion

    Further Information Favourable Opinion