Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35485
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dc.contributor.authorBurrell, Aidan-
dc.contributor.authorBailey, Michael J-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorBuscher, Hergen-
dc.contributor.authorEastwood, Glenn M-
dc.contributor.authorForrest, Paul-
dc.contributor.authorFraser, John F-
dc.contributor.authorFulcher, Bentley-
dc.contributor.authorGattas, David-
dc.contributor.authorHiggins, Alisa M-
dc.contributor.authorHodgson, Carol L-
dc.contributor.authorLitton, Edward-
dc.contributor.authorMartin, Emma-Leah-
dc.contributor.authorNair, Priya-
dc.contributor.authorNg, Sze J-
dc.contributor.authorOrford, Neil-
dc.contributor.authorOttosen, Kelly-
dc.contributor.authorPaul, Eldho-
dc.contributor.authorPellegrino, Vincent-
dc.contributor.authorReid, Liadain-
dc.contributor.authorShekar, Kiran-
dc.contributor.authorTotaro, Richard J-
dc.contributor.authorTrapani, Tony-
dc.contributor.authorUdy, Andrew-
dc.contributor.authorZiegenfuss, Marc-
dc.contributor.authorPilcher, David-
dc.date2024-
dc.date.accessioned2024-09-12T01:01:03Z-
dc.date.available2024-09-12T01:01:03Z-
dc.date.issued2024-09-
dc.identifier.citationIntensive Care Medicine 2024-09; 50(9)en_US
dc.identifier.issn1432-1238-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/35485-
dc.description.abstractPatients receiving venoarterial extracorporeal membrane oxygenation (VA-ECMO) frequently develop arterial hyperoxaemia, which may be harmful. However, lower oxygen saturation targets may also lead to harmful episodes of hypoxaemia. In this registry-embedded, multicentre trial, we randomly assigned adult patients receiving VA-ECMO in an intensive care unit (ICU) to either a conservative (target SaO2 92-96%) or to a liberal oxygen strategy (target SaO2 97-100%) through controlled oxygen administration via the ventilator and ECMO gas blender. The primary outcome was the number of ICU-free days to day 28. Secondary outcomes included ICU-free days to day 60, mortality, ECMO and ventilation duration, ICU and hospital lengths of stay, and functional outcomes at 6 months. From September 2019 through June 2023, 934 patients who received VA-ECMO were reported to the EXCEL registry, of whom 300 (192 cardiogenic shock, 108 refractory cardiac arrest) were recruited. We randomised 149 to a conservative and 151 to a liberal oxygen strategy. The median number of ICU-free days to day 28 was similar in both groups (conservative: 0 days [interquartile range (IQR) 0-13.7] versus liberal: 0 days [IQR 0-13.7], median treatment effect: 0 days [95% confidence interval (CI) - 3.1 to 3.1]). Mortality at day 28 (59/159 [39.6%] vs 59/151 [39.1%]) and at day 60 (64/149 [43%] vs 62/151 [41.1%] were similar in conservative and liberal groups, as were all other secondary outcomes and adverse events. The conservative group experienced 44 (29.5%) major protocol deviations compared to 2 (1.3%) in the liberal oxygen group (P < 0.001). In adults receiving VA-ECMO in ICU, a conservative compared to a liberal oxygen strategy, did not affect the number of ICU-free days to day 28.en_US
dc.language.isoeng-
dc.subjectECMOen_US
dc.subjectExtracorporeal membrane oxygenationen_US
dc.subjectHyperoxaemiaen_US
dc.subjectHyperoxiaen_US
dc.subjectOxygen targeten_US
dc.titleConservative or liberal oxygen targets in patients on venoarterial extracorporeal membrane oxygenation.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleIntensive Care Medicineen_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, Melbourne, VIC, 3004, Australia.;Department of Intensive Care and Hyperbaric Medicine, The Alfred, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationData Analytics Research and Evaluation (DARE) Centreen_US
dc.identifier.affiliationIntensive Careen_US
dc.identifier.affiliationIntensive Care Service, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.;Sydney Medical School, University of Sydney, Sydney, NSW, Australia.en_US
dc.identifier.affiliationInstitute of Molecular Bioscience, The University of Queensland, Herston, QLD, Australia.;Critical Care Research Group, The Prince Charles Hospital, Chermside, QLD, Australia.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, Melbourne, VIC, 3004, Australia.en_US
dc.identifier.affiliationIntensive Care Service, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.;Sydney Medical School, University of Sydney, Sydney, NSW, Australia.en_US
dc.identifier.affiliationIntensive Care Unit, Fiona Stanley Hospital, Murdoch, WA, Australia.;The Australian and New Zealand Intensive Care Society (ANZICS) Centre for Outcomes and Resources Evaluation, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Intensive Care and Hyperbaric Medicine, The Alfred, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationThe George Institute for Global Health, Newtown, NSW, Australia.;Intensive Care Unit, St Vincent's Hospital, Darlinghurst, NSW, Australia.;University of New South Wales, Sydney, NSW, Australia.en_US
dc.identifier.affiliationDepartment of Intensive Care and Hyperbaric Medicine, The Alfred, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationInstitute of Molecular Bioscience, The University of Queensland, Herston, QLD, Australia.;Adult Intensive Care Unit, The Prince Charles Hospital, Chermside, QLD, Australia.en_US
dc.identifier.affiliationIntensive Care Service, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.;Sydney Medical School, University of Sydney, Sydney, NSW, Australia.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, Melbourne, VIC, 3004, Australia.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, Melbourne, VIC, 3004, Australia.;Department of Intensive Care and Hyperbaric Medicine, The Alfred, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationCritical Care Research Group, The Prince Charles Hospital, Chermside, QLD, Australia.;Adult Intensive Care Unit, The Prince Charles Hospital, Chermside, QLD, Australia.en_US
dc.identifier.doi10.1007/s00134-024-07564-8en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-8939-7985en_US
dc.identifier.pubmedid39162827-
dc.description.volume50-
dc.description.issue9-
dc.description.startpage1470-
dc.description.endpage1483-
dc.subject.meshtermssecondaryExtracorporeal Membrane Oxygenation/methods-
dc.subject.meshtermssecondaryExtracorporeal Membrane Oxygenation/adverse effects-
dc.subject.meshtermssecondaryIntensive Care Units/statistics & numerical data-
dc.subject.meshtermssecondaryOxygen Saturation/physiology-
dc.subject.meshtermssecondaryRegistries/statistics & numerical data-
dc.subject.meshtermssecondaryShock, Cardiogenic/therapy-
dc.subject.meshtermssecondaryShock, Cardiogenic/mortality-
dc.subject.meshtermssecondaryHeart Arrest/therapy-
dc.subject.meshtermssecondaryHeart Arrest/mortality-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptIntensive Care-
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