Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20267
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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.authorDelaney, Anthony-
dc.contributor.authorCoggins, Andrew R-
dc.contributor.authorFatovich, Daniel M-
dc.contributor.authorFraser, John F-
dc.contributor.authorHarley, Amanda-
dc.contributor.authorJones, Peter-
dc.contributor.authorKinnear, Fran-
dc.contributor.authorMay, Katya-
dc.contributor.authorPeake, Sandra-
dc.contributor.authorTaylor, David McD-
dc.contributor.authorWilliams, Julian-
dc.contributor.authorWilliams, Patricia-
dc.date2019-
dc.date.accessioned2019-02-04T23:34:15Z-
dc.date.available2019-02-04T23:34:15Z-
dc.date.issued2019-
dc.identifier.citationEmergency Medicine Australasia : EMA 2019; 31(1): 90-96-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20267-
dc.description.abstractThere is uncertainty about the optimal i.v. fluid volume and timing of vasopressor commencement in the resuscitation of patients with sepsis and hypotension. We aim to study current resuscitation practices in EDs in Australia and New Zealand (the Australasian Resuscitation In Sepsis Evaluation: FLUid or vasopressors In Emergency Department Sepsis [ARISE FLUIDS] observational study). ARISE FLUIDS is a prospective, multicentre observational study in 71 hospitals in Australia and New Zealand. It will include adult patients presenting to the ED during a 30 day period with suspected sepsis and hypotension (systolic blood pressure <100 mmHg) despite at least 1000 mL fluid resuscitation. We will obtain data on baseline demographics, clinical and laboratory variables, all i.v. fluid given in the first 24 h, vasopressor use, time to antimicrobial administration, admission to intensive care, organ failure and in-hospital mortality. We will specifically describe (i) the volume of fluid administered at the following time points: when meeting eligibility criteria, in the first 6 h, at 24 h and prior to vasopressor commencement and (ii) the frequency and timing of vasopressor use in the first 6 h and at 24 h. Screening logs will provide reliable estimates of the proportion of ED patients meeting eligibility criteria for a subsequent randomised controlled trial. This multicentre, observational study will provide insight into current haemodynamic resuscitation practices in patients with sepsis and hypotension as well as estimates of practice variation and patient outcomes. The results will inform the design and feasibility of a multicentre phase III trial of early haemodynamic resuscitation in patients presenting to ED with sepsis and hypotension.-
dc.language.isoeng-
dc.subjectemergency department-
dc.subjectfluid therapy-
dc.subjecthypotension-
dc.subjectsepsis-
dc.subjectvasopressor-
dc.titleThe Australasian Resuscitation In Sepsis Evaluation: FLUid or vasopressors In Emergency Department Sepsis, a multicentre observational study (ARISE FLUIDS observational study): Rationale, methods and analysis plan.-
dc.typeJournal Article-
dc.identifier.journaltitleEmergency Medicine Australasia : EMA-
dc.identifier.affiliationSchool of Medicine, Griffith University, Gold Coast, Queensland, Australiaen
dc.identifier.affiliationEmergency Medicine and Trauma, Westmead Hospital, Sydney, New South Wales, 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.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.affiliationDepartment of Intensive Care, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationSchool of Medicine, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine and Radiology, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Intensive Care and Hyperbaric Medicine, The Alfred, Melbourne, Victoria, Australiaen
dc.identifier.affiliationSchool of Medicine, Bond University, Gold Coast, Queensland, Australiaen
dc.identifier.affiliationSchool of Medicine, The University of Western Australia, Perth, Western Australia, Australiaen
dc.identifier.affiliationDepartment of Surgery, The University of Auckland, Auckland, New Zealanden
dc.identifier.affiliationAdult Emergency Department, Auckland City Hospital, Auckland, New Zealanden
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 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.affiliationFaculty of Medicine, The University of Queensland, Brisbane, Queensland, Australiaen
dc.identifier.affiliationEmergency and Trauma Centre, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australiaen
dc.identifier.affiliationDepartment of Emergency Medicine, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Emergency Medicine, Gold Coast University Hospital, Gold Coast, Queensland, Australiaen
dc.identifier.affiliationEmergency and Children's Services, The Prince Charles Hospital, Brisbane, Queensland, Australiaen
dc.identifier.affiliationCritical Care Management Team, Queensland Children's Hospital, Brisbane, Queensland, Australiaen
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.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.doi10.1111/1742-6723.13223-
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.orcid0000-0001-9414-6905-
dc.identifier.orcid0000-0003-1560-1186-
dc.identifier.orcid0000-0002-8986-9997-
dc.identifier.orcid0000-0002-1650-8939-
dc.identifier.pubmedid30669181-
dc.type.austinJournal Article-
local.name.researcherBellomo, Rinaldo
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptEmergency-
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