Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32700
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dc.contributor.authorMacdonald, Stephen-
dc.contributor.authorBosio, Erika-
dc.contributor.authorKeijzers, Gerben-
dc.contributor.authorBurrows, Sally-
dc.contributor.authorHibbs, Moira-
dc.contributor.authorO'Donoghue, Helen-
dc.contributor.authorTaylor, David McD-
dc.contributor.authorMukherjee, Ashes-
dc.contributor.authorKinnear, Frances-
dc.contributor.authorSmart, Lisa-
dc.contributor.authorAscencio-Lane, Juan-Carlos-
dc.contributor.authorLitton, Edward-
dc.contributor.authorFraser, John-
dc.contributor.authorShapiro, Nathan I-
dc.contributor.authorArendts, Glenn-
dc.contributor.authorFatovich, Daniel-
dc.date2023-
dc.date.accessioned2023-04-21T00:55:20Z-
dc.date.available2023-04-21T00:55:20Z-
dc.date.issued2023-04-17-
dc.identifier.citationIntensive Care Medicine Experimental 2023-04-17; 11(1)en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32700-
dc.description.abstractTo investigate the effect of IV fluid resuscitation on endothelial glycocalyx (EG) shedding and activation of the vascular endothelium and inflammation. A planned biomarker sub-study of the REFRESH trial in which emergency department (ED) patients) with suspected sepsis and hypotension were randomised to a restricted fluid/early vasopressor regimen or IV fluid resuscitation with later vasopressors if required (usual care). Blood samples were collected at randomisation (T0) and at 3 h (T3), 6 h (T6)- and 24 h (T24) for measurement of a range of biomarkers if EG shedding, endothelial cell activation and inflammation. Blood samples were obtained in 95 of 99 enrolled patients (46 usual care, 49 restricted fluid). Differences in the change in biomarker over time between the groups were observed for Hyaluronan (2.2-fold from T3 to T24, p = 0.03), SYN-4 (1.5-fold from T3 to T24, P = 0.01) and IL-6 (2.5-fold from T0 to T3, p = 0.03). No difference over time was observed between groups for the other biomarkers. A consistent signal across a range of biomarkers of EG shedding or of endothelial activation or inflammation was not demonstrated. This could be explained by pre-existing EG shedding or overlap between the fluid volumes administered in the two groups in this clinical trial. Trial registration Australia New Zealand Clinical Trials Registry ACTRN126160000006448 Registered 12 January 2016.en_US
dc.language.isoeng-
dc.subjectEndothelial glycocalyxen_US
dc.subjectEndotheliumen_US
dc.subjectFluid therapyen_US
dc.subjectInflammationen_US
dc.subjectSepsisen_US
dc.titleEffect of intravenous fluid volume on biomarkers of endothelial glycocalyx shedding and inflammation during initial resuscitation of sepsis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleIntensive Care Medicine Experimentalen_US
dc.identifier.affiliationCentre for Clinical Research in Emergency Medicine, Harry Perkins Institute of Medical Research, Perth, WA, Australiaen_US
dc.identifier.affiliationMedical School, University of Western Australia, Perth, WA, Australia.en_US
dc.identifier.affiliationEmergency Department, Gold Coast University Hospital, Gold Coast, QLD, Australiaen_US
dc.identifier.affiliationResearch Foundation, Royal Perth Hospital, Perth, WA, Australia.en_US
dc.identifier.affiliationResearch Centre, Royal Perth Hospital, Perth, WA, Australia.en_US
dc.identifier.affiliationEmergency Department, Royal Perth Hospital, Perth, WA, Australia.en_US
dc.identifier.affiliationEmergencyen_US
dc.identifier.affiliationEmergency Department, Armadale Health Service, Perth, WA, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, University of Queensland, Brisbane, QLD, Australia.en_US
dc.identifier.affiliationSchool of Science, Health Engineering and Education, Murdoch University, Perth, WA, Australia.en_US
dc.identifier.affiliationEmergency Department, Royal Hobart Hospital, Hobart, TAS, Australia.en_US
dc.identifier.affiliationIntensive Care, Fiona Stanley Hospital, Perth, WA, Australia.en_US
dc.identifier.affiliationCritical Care Research Group, The Prince Charles Hospital, University of Queensland, Brisbane, QLD, Australia.en_US
dc.identifier.affiliationDepartment of Emergency Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.en_US
dc.identifier.affiliationEmergency Department, Fiona Stanley Hospital, Perth, WA, Australiaen_US
dc.identifier.affiliationFaculty of Health Sciences and Medicine, Bond University, Gold Coast, QLD, Australiaen_US
dc.identifier.affiliationSchool of Medicine, Griffith University, Gold Coast, QLD, Australiaen_US
dc.identifier.doi10.1186/s40635-023-00508-4en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-9921-4620en_US
dc.identifier.pubmedid37062769-
dc.description.volume11-
dc.description.issue1-
dc.description.startpage21-
local.name.researcherTaylor, David McD
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptEmergency-
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