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dc.contributor.authorWeiss, Raphael
dc.contributor.authorSaadat-Gilani, Khaschayar
dc.contributor.authorKerschke, Laura
dc.contributor.authorWempe, Carola
dc.contributor.authorMeersch, Melanie
dc.contributor.authorZarbock, Alexander
dc.contributor.authorMakhloufi, Hichem
dc.contributor.authorSağır, Özlem
dc.date.accessioned2022-10-06T07:54:21Z
dc.date.available2022-10-06T07:54:21Z
dc.date.issued2021en_US
dc.identifier.issn2044-6055
dc.identifier.urihttps://doi.org/10.1136/bmjopen-2021-055705
dc.identifier.urihttps://hdl.handle.net/20.500.12462/12577
dc.descriptionSağır, Özlem (Balikesir Author)en_US
dc.description.abstractIntroduction 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. ©en_US
dc.language.isoengen_US
dc.publisherBMJ Publishing Groupen_US
dc.relation.isversionof10.1136/bmjopen-2021-055705en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAcute Renal Failureen_US
dc.subjectAdult Intensive & Critical Careen_US
dc.subjectChronic Renal Failureen_US
dc.subjectEpidemiologyen_US
dc.subjectSurgeryen_US
dc.titleEPIdemiology of Surgery-Associated Acute Kidney Injury (EPIS-AKI): Study protocol for a multicentre, observational trialen_US
dc.typearticleen_US
dc.relation.journalBMJ Openen_US
dc.contributor.departmentTıp Fakültesien_US
dc.identifier.volume11en_US
dc.identifier.issue12en_US
dc.identifier.startpage1en_US
dc.identifier.endpage9en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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