Treatment Costs of Kidney Injury in Patients Having Heart Surgery in the UK

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe Royal Wolverhampton Hospitals NHS Trust

About this trial

Single-centre retrospective analysis of prospectively collected data with propensity matched scoring groups (AKI v/s non-AKI). Data collection from databases (or their equivalent): PATS Dendrite, Electronic Medical Records, TD-web (results Portal), MedTrack (ICU database), iSite (Radiology), SPY (Long-term status)

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Underwent elective or in-house urgent cardiac surgery at the Royal Wolverhampton NHS Trust between 1st January 2013 and 31st December 2025, excluding those who had surgery during 2020 and 2021 due to the confounding effect of COVID-19 on acute kidney injury incidence.

Cardiopulmonary bypass (CPB) was utilised during the cardiac surgical procedure.

A complete minimum dataset is available within the study databases, comprising: age, sex, history of diabetes, left ventricular ejection fraction (LVEF), surgical priority, pre-operative haemoglobin and serum creatinine (SCr) levels, type of cardiac surgery performed, CPB duration, EuroSCORE or logistic EuroSCORE, renal replacement therapy (RRT) use, and post-operative day 1 and/or day 2 and/or day 3 SCr values.

Disqualifiers

The procedure was performed as an emergency surgery.

Required data fields are incomplete or unavailable.

Surgery was performed off-pump, without the use of cardiopulmonary bypass.

The patient was dialysis-dependent prior to surgery.

Trial population

The study will include patients undergoing elective or in-hospital urgent cardiac surgery requiring cardiopulmonary bypass at the participating cardiac surgery centre.

Trial design

Design model

Case-control

Time perspective

Retrospective

Treatments tested in this trial

  • No Intervention: Observational Cohort

    Other intervention

    No intervention

Treatment groups

4,600 Participants
are divided into 2 treatment groups
Group A: Patients who developed AKI in their post-operative phase0 interventions
Group B: Patients who did not develop AKI in their post-operative phase1 intervention

Trial outcomes

Primary outcomes

1

Overall cost of treatment in £ for the each KDIGO stage of CSA-AKI

Based on the KDIGO clinical practice guidelines, AKI is defined in relation to the change in serum creatinine (SCr), use of RRT (Renal Replacement Therapy) and urine output. For this study, CSA-AKI is defined (modified KDIGO) as when any one of the following three criteria are met: 1. An increase in serum creatinine (SCr) by ≥0.3 mg/dl (≥26.5 micromol/l) within 72 hours of surgery compared to the baseline value; or 2. An increase in SCr by ≥1.5 times from SCr value at baseline within 72 hours of surgery; or 3. Use of RRT within 7 days of surgery.

Time frame
From date each patient had surgery to the date each patient discharged from hospital, for all eligible patients who underwent surgery between 1st January 2013 and 31st December 2025 (varies from patient to patient), assessed at point of data extraction

Secondary outcomes

1

Number of patients with CSA-AKI

Incidence of CSA-AKI overall and by KDIGO stage

Time frame
From date each patient had surgery to date each patient discharged from hospital, for all eligible patients who underwent surgery between 1st January 2013 and 31st December 2025 (varies from patient to patient), , assessed at point of data extraction
2

Days patient spent in ICU

Duration of patient's ICU stay following surgery (days)

Time frame
From date each patient had surgery to date each patient discharged from ICU, for all eligible patients who underwent surgery between 1st January 2013 and 31st December 2025 (varies from patient to patient), assessed at point of data extraction
3

Average cost of ICU stay in £ for each KDIGO CSA-AKI stage

Costs of ICU stay (HRG) for the KDIGO CSA-AKI stages

Time frame
From date each patient had surgery to date each patient discharged from ICU, for all eligible patients who underwent surgery between 1st January 2013 and 31st December 2025 (varies from patient to patient), assessed at point of data extraction
4

Length of time each patient spent in hospital in days

In-hospital stay duration (days)

Time frame
From date each patient had surgery to date each patient discharged from hospital, for all eligible patients who underwent surgery between 1st January 2013 and 31st December 2025 (varies from patient to patient), assessed at point of data extraction

Other outcomes

Sponsors and contacts

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