Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22611
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dc.contributor.authorKeijzers, Gerben-
dc.contributor.authorMacdonald, Stephen Pj-
dc.contributor.authorUdy, Andrew A-
dc.contributor.authorArendts, Glenn-
dc.contributor.authorBailey, Michael-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorBlecher, Gabriel E-
dc.contributor.authorBurcham, Jonathon-
dc.contributor.authorCoggins, Andrew R-
dc.contributor.authorDelaney, Anthony-
dc.contributor.authorFatovich, Daniel M-
dc.contributor.authorFraser, John F-
dc.contributor.authorHarley, Amanda-
dc.contributor.authorJones, Peter-
dc.contributor.authorKinnear, Frances B-
dc.contributor.authorMay, Katya-
dc.contributor.authorPeake, Sandra-
dc.contributor.authorTaylor, David McD-
dc.contributor.authorWilliams, Patricia-
dc.date2020-02-10-
dc.date.accessioned2020-02-18T22:28:58Z-
dc.date.available2020-02-18T22:28:58Z-
dc.date.issued2020-08-
dc.identifier.citationEmergency Medicine Australasia : EMA 2020; 32(4): 586-598-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22611-
dc.description.abstractTo describe haemodynamic resuscitation practices in ED patients with suspected sepsis and hypotension. This was a prospective, multicentre, observational study conducted in 70 hospitals in Australia and New Zealand between September 2018 and January 2019. Consecutive adults presenting to the ED during a 30-day period at each site, with suspected sepsis and hypotension (systolic blood pressure <100 mmHg) despite at least 1000 mL fluid resuscitation, were eligible. Data included baseline demographics, clinical and laboratory variables and intravenous fluid volume administered, vasopressor administration at baseline and 6- and 24-h post-enrolment, time to antimicrobial administration, intensive care admission, organ support and in-hospital mortality. A total of 4477 patients were screened and 591 were included with a mean (standard deviation) age of 62 (19) years, Acute Physiology and Chronic Health Evaluation II score 15.2 (6.6) and a median (interquartile range) systolic blood pressure of 94 mmHg (87-100). Median time to first intravenous antimicrobials was 77 min (42-148). A vasopressor infusion was commenced within 24 h in 177 (30.2%) patients, with noradrenaline the most frequently used (n = 138, 78%). A median of 2000 mL (1500-3000) of intravenous fluids was administered prior to commencing vasopressors. The total volume of fluid administered from pre-enrolment to 24 h was 4200 mL (3000-5661), with a range from 1000 to 12 200 mL. Two hundred and eighteen patients (37.1%) were admitted to an intensive care unit. Overall in-hospital mortality was 6.2% (95% confidence interval 4.4-8.5%). Current resuscitation practice in patients with sepsis and hypotension varies widely and occupies the spectrum between a restricted volume/earlier vasopressor and liberal fluid/later vasopressor strategy.-
dc.language.isoeng-
dc.subjectemergency department-
dc.subjectfluid therapy-
dc.subjecthypotension-
dc.subjectsepsis-
dc.subjectvasopressor-
dc.titleThe Australasian Resuscitation In Sepsis Evaluation: Fluids or vasopressors in emergency department sepsis (ARISE FLUIDS), a multi-centre observational study describing current practice in Australia and New Zealand.-
dc.typeJournal Article-
dc.identifier.journaltitleEmergency Medicine Australasia : EMA-
dc.identifier.affiliationAdult Emergency Department, Auckland City Hospital, Auckland, New Zealanden
dc.identifier.affiliationCritical Care Research Group, The Prince Charles Hospital, Brisbane, Queensland, Australiaen
dc.identifier.affiliationIntensive Care Unit, St Andrew's War Memorial Hospital, Brisbane, Queensland, Australiaen
dc.identifier.affiliationCritical Care Management Team, Queensland Children's Hospital, Brisbane, Queensland, Australiaen
dc.identifier.affiliationThe University of Queensland, Brisbane, Queensland, Australiaen
dc.identifier.affiliationEmergency and Children's Services, The Prince Charles Hospital, Brisbane, Queensland, Australiaen
dc.identifier.affiliationDepartment of Intensive Care Medicine, The Queen Elizabeth Hospital, Adelaide, South Australia, Australiaen
dc.identifier.affiliationFaculty of Health and Medical Sciences, School of Medicine, Adelaide University, Adelaide, South Australia, Australiaen
dc.identifier.affiliationSchool of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationEmergency Medicine Research, Department of Emergency Medicine, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationSchool of Medicine, The University of Western Australia, Perth, Western Australia, Australiaen
dc.identifier.affiliationSchool of Medicine, The University of Auckland, Auckland, New Zealanden
dc.identifier.affiliationEmergency Medicine and Trauma, Westmead Hospital, Sydney, New South Wales, Australiaen
dc.identifier.affiliationDepartment of Emergency Medicine, Gold Coast University Hospital, Gold Coast, Queensland, Australiaen
dc.identifier.affiliationSchool of Medicine, Bond University, Gold Coast, Queensland, Australiaen
dc.identifier.affiliationSchool of Medicine, Griffith University, Gold Coast, Queensland, Australiaen
dc.identifier.affiliationCentre for Clinical Research in Emergency Medicine, Harry Perkins Institute of Medical Research, Perth, Western Australia, Australiaen
dc.identifier.affiliationEmergency Department, Royal Perth Hospital, The University of Western Australia, Perth, Western Australia, Australiaen
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Intensive Care and Hyperbaric Medicine, The Alfred, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine and Radiology, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Intensive Care, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationSchool of Medicine, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationEmergency Department, Monash Medical Centre, Monash Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationMonash Emergency Research Collaborative, School of Clinical Sciences at Monash Health, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationMalcolm Fisher Department of Intensive Care Medicine, Royal North Shore Hospital, Sydney, New South Wales, Australiaen
dc.identifier.affiliationNorthern Clinical School, Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australiaen
dc.identifier.affiliationDivision of Critical Care and Trauma, The George Institute for Global Health, The University of New South Wales, Sydney, New South Wales, Australiaen
dc.identifier.affiliationFaculty of Medicine, The University of Queensland, Brisbane, Queensland, Australiaen
dc.identifier.doi10.1111/1742-6723.13469-
dc.identifier.orcid0000-0003-1100-4552-
dc.identifier.orcid0000-0001-9921-4620-
dc.identifier.orcid0000-0002-6284-2022-
dc.identifier.orcid0000-0001-7830-7756-
dc.identifier.orcid0000-0001-8537-2011-
dc.identifier.orcid0000-0002-5652-6920-
dc.identifier.orcid0000-0002-1015-7146-
dc.identifier.orcid0000-0001-9414-6905-
dc.identifier.orcid0000-0003-1560-1186-
dc.identifier.orcid0000-0002-8986-9997-
dc.identifier.orcid0000-0002-1650-8939-
dc.identifier.pubmedid32043315-
dc.type.austinJournal Article-
local.name.researcherBellomo, Rinaldo
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.deptEmergency-
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