Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34014
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dc.contributor.authorWald, Ron-
dc.contributor.authorGaudry, Stephane-
dc.contributor.authorda Costa, Bruno R-
dc.contributor.authorAdhikari, Neill K J-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorDu, Bin-
dc.contributor.authorGallagher, Martin P-
dc.contributor.authorHoste, Eric A-
dc.contributor.authorLamontagne, François-
dc.contributor.authorJoannidis, Michael-
dc.contributor.authorLiu, Kathleen D-
dc.contributor.authorMcAuley, Daniel F-
dc.contributor.authorMcGuinness, Shay P-
dc.contributor.authorNichol, Alistair D-
dc.contributor.authorOstermann, Marlies-
dc.contributor.authorPalevsky, Paul M-
dc.contributor.authorQiu, Haibo-
dc.contributor.authorPettilä, Ville-
dc.contributor.authorSchneider, Antoine G-
dc.contributor.authorSmith, Orla M-
dc.contributor.authorVaara, Suvi T-
dc.contributor.authorWeir, Matthew-
dc.contributor.authorDreyfuss, Didier-
dc.contributor.authorBagshaw, Sean M-
dc.date2023-
dc.date.accessioned2023-10-18T03:29:39Z-
dc.date.available2023-10-18T03:29:39Z-
dc.date.issued2023-11-
dc.identifier.citationIntensive Care Medicine 2023-11; 49(11)en_US
dc.identifier.issn1432-1238-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34014-
dc.description.abstractThere is controversy regarding the optimal renal-replacement therapy (RRT) modality for critically ill patients with acute kidney injury (AKI). We conducted a secondary analysis of the STandard versus Accelerated Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial to compare outcomes among patients who initiated RRT with either continuous renal replacement therapy (CRRT) or intermittent hemodialysis (IHD). We generated a propensity score for the likelihood of receiving CRRT and used inverse probability of treatment with overlap-weighting to address baseline inter-group differences. The primary outcome was a composite of death or RRT dependence at 90-days after randomization. We identified 1590 trial participants who initially received CRRT and 606 who initially received IHD. The composite outcome of death or RRT dependence at 90-days occurred in 823 (51.8%) patients who commenced CRRT and 329 (54.3%) patients who commenced IHD (unadjusted odds ratio (OR) 0.90; 95% confidence interval (CI) 0.75-1.09). After balancing baseline characteristics with overlap weighting, initial receipt of CRRT was associated with a lower risk of death or RRT dependence at 90-days compared with initial receipt of IHD (OR 0.81; 95% CI 0.66-0.99). This association was predominantly driven by a lower risk of RRT dependence at 90-days (OR 0.61; 95% CI 0.39-0.94). In critically ill patients with severe AKI, initiation of CRRT, as compared to IHD, was associated with a significant reduction in the composite outcome of death or RRT dependence at 90-days.en_US
dc.language.isoeng-
dc.subjectAcute kidney injuryen_US
dc.subjectContinuousen_US
dc.subjectIntermittent hemodialysisen_US
dc.subjectModalityen_US
dc.subjectMortalityen_US
dc.subjectRandomized trialen_US
dc.subjectRenal-replacement therapyen_US
dc.titleInitiation of continuous renal replacement therapy versus intermittent hemodialysis in critically ill patients with severe acute kidney injury: a secondary analysis of STARRT-AKI trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleIntensive Care Medicineen_US
dc.identifier.affiliationDivision of Nephrology, St. Michael's Hospital, University of Toronto, Li Ka Shing Knowledge Institute, Toronto, ON, Canada.en_US
dc.identifier.affiliationAP-HP, Hôpital Avicenne, Service de Réanimation Médico-Chirurgicale, UFR SMBH, Université Sorbonne Paris Nord, Bobigny, France.;UMR S1155, French National Institute of Health and Medical Research (INSERM), CORAKID, Hôpital Tenon, Sorbonne Université, 75020, Paris, France.en_US
dc.identifier.affiliationClinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.en_US
dc.identifier.affiliationDepartment of Critical Care Medicine, Sunnybrook Health Sciences Centre and University of Toronto, Toronto, Canada.en_US
dc.identifier.affiliationIntensive Careen_US
dc.identifier.affiliationDepartment of Critical Care Medicine, Peking Union Medical College Hospital, Beijing, China.en_US
dc.identifier.affiliationThe George Institute for Global Health, University of New South Wales, Kensington, NSW, Australia.en_US
dc.identifier.affiliationIntensive Care Unit, Department of Internal Medicine and Pediatrics, Ghent University Hospital, Ghent University, Ghent, Belgium.en_US
dc.identifier.affiliationDepartment of Medicine, Université de Sherbrooke, Centre de Recherche du CHU de Sherbrooke, Sherbrooke, QC, Canada.en_US
dc.identifier.affiliationDivision of Intensive Care and Emergency Medicine, Department of Internal Medicine, Medical University Innsbruck, Innsbruck, Austria.en_US
dc.identifier.affiliationDivision of Intensive Care and Nephrology, University of California San Francisco, San Francisco, CA, USA.en_US
dc.identifier.affiliationThe Regional Intensive Care Unit, The Wellcome-Wolfson Institute for Experimental Medicine, Queen's University, Royal Victoria Hospital, Belfast, UK.en_US
dc.identifier.affiliationCardiothoracic and Vascular Intensive Care Unit, Auckland City Hospital, Auckland and Medical Research Institute of New Zealand, Wellington, New Zealand.en_US
dc.identifier.affiliationDepartment of Critical Care Medicine, University College Dublin Clinical Research Centre at St. Vincent's University Hospital, Dublin, Ireland.;Monash University, Melbourne, Australia.en_US
dc.identifier.affiliationDepartment of Critical Care Medicine, King's College London, Guy's & St Thomas Hospital, London, UK.en_US
dc.identifier.affiliationRenal-Electrolyte Division, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.;Kidney Medicine Section, VA Pittsburgh Healthcare System, Pittsburgh, PA, USA.en_US
dc.identifier.affiliationDepartment of Critical Care Medicine, Zhongda Hospital Southeast University, Nanjing, China.en_US
dc.identifier.affiliationDivision of Intensive Care Medicine, Department of Perioperative, Intensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.en_US
dc.identifier.affiliationDepartment of Critical Care Medicine Centre, Hospitalier Universitaire Vaudois, Lausanne, Switzerland.en_US
dc.identifier.affiliationDepartment of Critical Care, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Canada.en_US
dc.identifier.affiliationDepartment of Intensive Care Medicine, Department of Anesthesiology, Intensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.en_US
dc.identifier.affiliationDivision of Nephrology, London Health Sciences Centre, London, ON, Canada.en_US
dc.identifier.affiliationUMR S1155, French National Institute of Health and Medical Research (INSERM), CORAKID, Hôpital Tenon, Sorbonne Université, 75020, Paris, France.;Service de Médecine Intensive Réanimation, Sorbonne Université, Hôpital Louis Mourier, Assistance Publique, Université de Paris-Cité, Paris, France.en_US
dc.identifier.affiliationDepartment of Critical Care Medicine, Faculty of Medicine and Dentistry, University of Alberta, and Alberta Health Services, Edmonton, AB, Canada.en_US
dc.identifier.doi10.1007/s00134-023-07211-8en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-4411-8169en_US
dc.identifier.pubmedid37815560-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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