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

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dc.contributor.author Coca, Armando
dc.contributor.author Bustamante-Munguira, Elena
dc.contributor.author Fidalgo, Verónica
dc.contributor.author Fernández, Manuel
dc.contributor.author Abad, Cristina
dc.contributor.author Franco, Marta
dc.contributor.author González-Pinto, Ángel
dc.contributor.author Pereda, Daniel
dc.contributor.author Cánovas, Sergio
dc.contributor.author Bustamante-Munguira, Juan
dc.date.accessioned 2025-11-19T15:39:34Z
dc.date.available 2025-11-19T15:39:34Z
dc.date.issued 2024-08-13
dc.identifier.citation Coca A, Bustamante-Munguira E, Fidalgo V, Fernández M, Abad C, Franco M, et al. EValuating the Effect of periopeRaTIve empaGliflOzin on cardiac surgery associated acute kidney injury: rationale and design of the VERTIGO study. Clinical Kidney Journal. 1 de agosto de 2024;17(8):sfae229.
dc.identifier.issn 2048-8505
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21393
dc.description.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.
dc.language.iso eng
dc.publisher OXFORD UNIV PRESS
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/ *
dc.title EValuating the Effect of periopeRaTIve empaGliflOzin on cardiac surgery associated acute kidney injury: rationale and design of the VERTIGO study
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 39139185
dc.relation.publisherversion https://academic.oup.com/ckj/article/doi/10.1093/ckj/sfae229/7718102
dc.identifier.doi 10.1093/ckj/sfae229
dc.journal.title Clinical Kidney Journal
dc.identifier.essn 2048-8513


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