Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22570
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dc.contributor.authorVaara, Suvi T-
dc.contributor.authorOstermann, Marlies-
dc.contributor.authorSelander, Tuomas-
dc.contributor.authorBitker, Laurent-
dc.contributor.authorSchneider, Antoine-
dc.contributor.authorPoli, Elettra-
dc.contributor.authorHoste, Eric-
dc.contributor.authorJoannidis, Michael-
dc.contributor.authorZarbock, Alexander-
dc.contributor.authorvan Haren, Frank-
dc.contributor.authorProwle, John-
dc.contributor.authorPettilä, Ville-
dc.contributor.authorBellomo, Rinaldo-
dc.date2020-02-05-
dc.date.accessioned2020-02-11T01:18:16Z-
dc.date.available2020-02-11T01:18:16Z-
dc.date.issued2020-02-26-
dc.identifier.citationActa Anaesthesiologica Scandinavica 2020; 64(6): 831-838-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22570-
dc.description.abstractFluid accumulation frequently coexists with acute kidney injury (AKI) and is associated with increased risk for AKI progression and mortality. Among septic shock patients, restricted use of resuscitation fluid has been reported to reduce the risk of worsening of AKI. Restrictive fluid therapy, however, has not been studied in the setting of established AKI. Here, we present the protocol and statistical analysis plan of the REstricted fluid therapy VERsus Standard trEatment in Acute Kidney Injury - the REVERSE-AKI trial that compares a restrictive fluid therapy regimen to standard therapy in critically ill patients with AKI. REVERSE-AKI is an investigator-initiated, multinational, open-label, randomized, controlled, feasibility pilot trial conducted in 7 ICUs in 5 countries. We aim to randomize 100 critically ill patients with AKI to a restrictive fluid treatment regimen versus standard management. In the restrictive fluid therapy regimen, the daily fluid balance target is neutral or negative. The primary outcome is the cumulative fluid balance assessed after 72 hrs from randomization. Secondary outcomes include safety, feasibility, duration and severity of AKI, and outcome at 90 days (mortality and dialysis dependence). This is the first multinational trial investigating the feasibility and safety of a restrictive fluid therapy regimen in critically ill patients with AKI.-
dc.language.isoeng-
dc.subjectacute kidney injury-
dc.subjectcritically ill-
dc.subjectfluid balance-
dc.subjectrestrictive fluid therapy-
dc.titleProtocol and statistical analysis plan for the REstricted fluid therapy VERsus Standard trEatment in Acute Kidney Injury - REVERSE-AKI randomized controlled pilot trial.-
dc.typeJournal Article-
dc.identifier.journaltitleActa Anaesthesiologica Scandinavica -
dc.identifier.affiliationDepartment of Anesthesiology, Intensive Care and Pain Medicine, University Hospital Münster, Münster, Germanyen
dc.identifier.affiliationAdult Intensive Care Unit, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerlanden
dc.identifier.affiliationCritical Care and Preoperative Medicine Research Group, Centre for Translational Medicine and Therapeutics, William Harvey Research Institute, Queen Mary University of London, London, UKen
dc.identifier.affiliationIntensive Care Unit, Ghent University Hospital, Ghent University, Ghent, Belgiumen
dc.identifier.affiliationUniversité de Lyon, CREATIS CNRS UMR5220 INSERM U1044 INSA-Lyon, Lyon, Franceen
dc.identifier.affiliationSchool of Medicine, The University of Melbourne, Melbourne, Australiaen
dc.identifier.affiliationKing's College London, Guy's & St Thomas' Hospital, Department of Critical Care, London, UKen
dc.identifier.affiliationIntensive Care Unit, Canberra Hospital, Canberra, Australiaen
dc.identifier.affiliationAustralian National University Medical School, Canberra, Australiaen
dc.identifier.affiliationDepartment of Intensive Care, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDivision of Intensive Care Medicine, Department of Anesthesiology, Intensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finlanden
dc.identifier.affiliationScience Service Center, Kuopio University Hospital, Kuopio, Finland..-
dc.identifier.affiliationDivision of Intensive Care and Emergency Medicine, Department of Internal Medicine, Medical University of Innsbruck, Austria..-
dc.identifier.doi10.1111/aas.13557-
dc.identifier.orcid0000-0002-3921-4423-
dc.identifier.orcid0000-0002-1650-8939-
dc.identifier.pubmedid32022904-
dc.type.austinJournal Article-
local.name.researcherBellomo, Rinaldo
item.languageiso639-1en-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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