EValuating the Effect of periopeRaTIve empaGliflOzin on cardiac surgery associated acute kidney injury: rationale and design of the VERTIGO study

Author:

Coca Armando12ORCID,Bustamante-Munguira Elena23,Fidalgo Verónica4,Fernández Manuel5,Abad Cristina6,Franco Marta3,González-Pinto Ángel7,Pereda Daniel8ORCID,Cánovas Sergio5,Bustamante-Munguira Juan910

Affiliation:

1. Department of Nephrology, Hospital Clínico Universitario , Valladolid , Spain

2. Department of Medicine, Dermatology, and Toxicology, Facultad de Medicina, Universidad de Valladolid , Valladolid , Spain

3. Department of Intensive Care Medicine, Hospital Clínico Universitario , Valladolid , Spain

4. Department of Nephrology, Hospital Virgen de la Concha , Zamora , Spain

5. Department of Cardiovascular Surgery, Hospital Clínico Universitario Virgen de la Arrixaca , Murcia , Spain

6. Department of Immunology, Hospital Clínico Universitario , Valladolid , Spain

7. Department of Cardiovascular Surgery, Hospital General Universitario Gregorio Marañón , Madrid , Spain

8. Department of Cardiovascular Surgery, Hospital Clinic de Barcelona, Barcelona , Spain

9. Department of Cardiovascular Surgery, Hospital Clínico Universitario , Valladolid , Spain

10. Department of Surgery, Facultad de Medicina, Universidad de Valladolid , Valladolid , Spain

Abstract

ABSTRACT Background Cardiac surgery-associated acute kidney injury (CSA-AKI) is a serious complication in patients undergoing cardiac surgery with extracorporeal circulation (ECC) that increases postoperative complications and mortality. CSA-AKI develops due to a combination of patient- and surgery-related risk factors that enhance renal ischemia–reperfusion injury. Sodium-glucose cotransporter 2 inhibitors (SGLT2i) such as empagliflozin reduce renal glucose reabsorption, improving tubulo-glomerular feedback, reducing inflammation and decreasing intraglomerular pressure. Preclinical studies have observed that SGLT2i may provide significant protection against renal ischemia–reperfusion injury due to their effects on inadequate mitochondrial function, reactive oxygen species activity or renal peritubular capillary congestion, all hallmarks of CSA-AKI. The VERTIGO (EValuating the Effect of periopeRaTIve empaGliflOzin) trial is a Phase 3, investigator-initiated, randomized, double-blind, placebo-controlled, multicenter study that aims to explore whether empagliflozin can reduce the incidence of adverse renal outcomes in cardiac surgery patients. Methods The VERTIGO study (EudraCT: 2021-004938-11) will enroll 608 patients that require elective cardiac surgery with ECC. Patients will be randomly assigned in a 1:1 ratio to receive either empagliflozin 10 mg orally daily or placebo. Study treatment will start 5 days before surgery and will continue during the first 7 days postoperatively. All participants will receive standard care according to local practice guidelines. The primary endpoint of the study will be the proportion of patients that develop major adverse kidney events during the first 90 days after surgery, defined as ≥25% renal function decline, renal replacement therapy initiation or death. Secondary, tertiary and safety endpoints will include rates of AKI during index hospitalization, postoperative complications and observed adverse events. Conclusions The VERTIGO trial will describe the efficacy and safety of empagliflozin in preventing CSA-AKI. Patient recruitment is expected to start in May 2024.

Funder

Gerencia Regional de Salud de Castilla y León

Publisher

Oxford University Press (OUP)

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