Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20870
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dc.contributor.authorWigmore, Geoffrey J-
dc.contributor.authorAnstey, James R-
dc.contributor.authorSt John, Ashley-
dc.contributor.authorGreaney, Joel-
dc.contributor.authorMorales-Codina, Marc-
dc.contributor.authorPresneill, Jeffrey J-
dc.contributor.authorDeane, Adam M-
dc.contributor.authorMacIsaac, Christopher M-
dc.contributor.authorBailey, Michael-
dc.contributor.authorTatoulis, James-
dc.contributor.authorBellomo, Rinaldo-
dc.date2019-03-28-
dc.date.accessioned2019-06-05T01:28:44Z-
dc.date.available2019-06-05T01:28:44Z-
dc.date.issued2019-11-
dc.identifier.citationJournal of Cardiothoracic and Vascular Anesthesia 2019; 33(11): 2920-2927en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20870-
dc.description.abstractTo compare the effects of fluid bolus therapy using 20% albumin versus crystalloid on fluid balance, hemodynamic parameters, and intensive care unit (ICU) treatment effects in post-cardiac surgery patients. Sequential period open-label pilot study. University teaching hospital. One hundred adult cardiac surgery patients who were prescribed fluid bolus therapy to correct hypotension or perceived hypovolemia or to optimize cardiac index during the first 24 hours in the ICU. The first 50 patients were treated with crystalloid fluid bolus therapy in the first period (control), and 50 patients with up to 2 treatments of 100 mL of 20% albumin fluid bolus therapy in the second period (intervention), followed by crystalloid therapy if needed. Demographic characteristics were similar at baseline. The intervention was associated with a less positive median fluid balance in the first 24 hours (albumin: 1,100 [650-1,960] v crystalloid: 1,970 [1,430-2,550] p = 0.001), fewer episodes of fluid bolus therapy (3 [2-5] v 5 [4-7]; p < 0.0001) and a lesser volume of fluid bolus therapy (700 [200-1,450] v 1,500 mL/24 h [1,100-2,250]; p < 0.0001). The intervention also was associated with a decreased median overall dose of norepinephrine in the first 24 hours of ICU stay (19 [0-52] v 47 µg/kg/24 hours [0-134]; p = 0.025) and shorter median time to cessation of norepinephrine (17 [5-28] v 28 hours [20-48]; p = 0.002). Post-cardiac surgery fluid bolus therapy with 20% albumin when compared with crystalloid fluid resulted in less positive fluid balance as well as several hemodynamic and potential ICU treatment advantages.en
dc.language.isoeng-
dc.subjectalbuminen
dc.subjectcardiac surgeryen
dc.subjectcrystalloiden
dc.subjectfluid balanceen
dc.subjectfluid bolusen
dc.subjectresuscitationen
dc.title20% Human Albumin Solution Fluid Bolus Administration Therapy in Patients After Cardiac Surgery (the HAS FLAIR Study).en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Cardiothoracic and Vascular Anesthesiaen
dc.identifier.affiliationDepartment of Cardiothoracic Surgery, Royal Melbourne Hospital, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Intensive Care, Royal Melbourne Hospital, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine and Radiology, University of Melbourne, Australiaen
dc.identifier.affiliationUniversity of Melbourne, Department of Medicine, Royal Melbourne Hospital, Parkville, Australiaen
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, The Alfred Centre, Melbourne, Victoria, Australiaen
dc.identifier.affiliationIntensive Careen
dc.identifier.doi10.1053/j.jvca.2019.03.049en
dc.type.contentTexten
dc.identifier.orcid0000-0002-1650-8939en
dc.identifier.pubmedid31097338-
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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