EPIdemiology of Surgery-Associated Acute Kidney Injury (EPIS-AKI): study protocol for a multicentre, observational trial

Abstract

Introduction: More than 300 million surgical procedures are performed each year. Acute kidney injury (AKI) is a common complication after major surgery and is associated with adverse short-term and long-term outcomes. However, there is a large variation in the incidence of reported AKI rates. The establishment of an accurate epidemiology of surgery-associated AKI is important for healthcare policy, quality initiatives, clinical trials, as well as for improving guidelines. The objective of the Epidemiology of Surgery-associated Acute Kidney Injury (EPIS-AKI) trial is to prospectively evaluate the epidemiology of AKI after major surgery using the latest Kidney Disease: Improving Global Outcomes (KDIGO) consensus definition of AKI.

Methods and analysis: EPIS-AKI is an international prospective, observational, multicentre cohort study including 10 000 patients undergoing major surgery who are subsequently admitted to the ICU or a similar high dependency unit. The primary endpoint is the incidence of AKI within 72 hours after surgery according to the KDIGO criteria. Secondary endpoints include use of renal replacement therapy (RRT), mortality during ICU and hospital stay, length of ICU and hospital stay and major adverse kidney events (combined endpoint consisting of persistent renal dysfunction, RRT and mortality) at day 90. Further, we will evaluate preoperative and intraoperative risk factors affecting the incidence of postoperative AKI. In an add-on analysis, we will assess urinary biomarkers for early detection of AKI.

Ethics and dissemination: EPIS-AKI has been approved by the leading Ethics Committee of the Medical Council North Rhine-Westphalia, of the Westphalian Wilhelms-University Münster and the corresponding Ethics Committee at each participating site. Results will be disseminated widely and published in peer-reviewed journals, presented at conferences and used to design further AKI-related trials.

Trial registration number: NCT04165369.

Keywords: acute renal failure; adult intensive & critical care; chronic renal failure; epidemiology; surgery.

Conflict of interest statement

Competing interests: None declared.

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Figures

Figure 1

EPIS-AKI Trial Workflow Research coordinators will screen patients for eligibility on a daily basis and then ask patients for study participation. After surgery, inclusion/exclusion criteria will be rechecked and if still eligible (especially duration of surgery ≥2 hours, admission to ICU or similar), patients will be enrolled and included in the trial. All subjects will be treated according to the standards of the local centres. Patients will be monitored closely for the first postoperative 72 hours during their stay on a high dependency unit. In addition, in selected study sites urine samples will be collected directly from the routinely inserted urine catheter immediately after surgery. AKI, acute kidney injury; EPIS-AKI, Epidemiology of Surgery-associated Acute Kidney Injury; ICU, intensive care unit, PACU; post anesthesia care unit, MAKE90; major adverse kidney events at day 90.