Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16995
Full metadata record
DC FieldValueLanguage
dc.contributor.authorCooper, D James-
dc.contributor.authorMcQuilten, Zoe K-
dc.contributor.authorNichol, Alistair-
dc.contributor.authorAdy, Bridget-
dc.contributor.authorAubron, Cécile-
dc.contributor.authorBailey, Michael-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorGantner, Dashiell-
dc.contributor.authorIrving, David O-
dc.contributor.authorKaukonen, Kirsi-Maija-
dc.contributor.authorMcArthur, Colin-
dc.contributor.authorMurray, Lynne-
dc.contributor.authorPettilä, Ville-
dc.contributor.authorFrench, Craig-
dc.contributor.authorTRANSFUSE Investigators-
dc.contributor.authorAustralian and New Zealand Intensive Care Society Clinical Trials Group-
dc.date2017-09-27-
dc.date.accessioned2017-12-08T03:11:17Z-
dc.date.available2017-12-08T03:11:17Z-
dc.date.issued2017-11-
dc.identifier.citationThe New England Journal of Medicine 2017; 377: 1858-1867en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16995-
dc.description.abstractBACKGROUND: It is uncertain whether the duration of red-cell storage affects mortality after transfusion among critically ill adults. METHODS: In an international, multicenter, randomized, double-blind trial, we assigned critically ill adults to receive either the freshest available, compatible, allogeneic red cells (short-term storage group) or standard-issue (oldest available), compatible, allogeneic red cells (long-term storage group). The primary outcome was 90-day mortality. RESULTS: From November 2012 through December 2016, at 59 centers in five countries, 4994 patients underwent randomization and 4919 (98.5%) were included in the primary analysis. Among the 2457 patients in the short-term storage group, the mean storage duration was 11.8 days. Among the 2462 patients in the long-term storage group, the mean storage duration was 22.4 days. At 90 days, there were 610 deaths (24.8%) in the short-term storage group and 594 (24.1%) in the long-term storage group (absolute risk difference, 0.7 percentage points; 95% confidence interval [CI], -1.7 to 3.1; P=0.57). At 180 days, the absolute risk difference was 0.4 percentage points (95% CI, -2.1 to 3.0; P=0.75). Most of the prespecified secondary measures showed no significant between-group differences in outcome. CONCLUSIONS: The age of transfused red cells did not affect 90-day mortality among critically ill adults. (Funded by the Australian National Health and Medical Research Council and others; TRANSFUSE Australian and New Zealand Clinical Trials Registry number, ACTRN12612000453886 ; ClinicalTrials.gov number, NCT01638416 .).en_US
dc.subjectBlood Preservationen_US
dc.subjectErythrocyte Transfusion/mortalityen_US
dc.subjectCritical Illness/therapyen_US
dc.titleAge of Red Cells for Transfusion and Outcomes in Critically Ill Adultsen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThe New England Journal of Medicineen_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Intensive Care, Alfred Hospital, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Haematology, Monash Health, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Intensive Care, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationThe University of Melbourne, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationResearch and Development, Australian Red Cross Blood Service, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationIrish Critical Care Clinical Trials Network, University College Dublin Clinical Research Centre at St. Vincent's University Hospital, Dublinen_US
dc.identifier.affiliationDépartement de Médecine Intensive Réanimation, Brest University Hospital, Brest, Franceen_US
dc.identifier.affiliationDepartment of Anesthesiology, University of Helsinki and Helsinki University Hospital, Helsinkien_US
dc.identifier.affiliationDivision of Intensive Care, University of Helsinki and Helsinki University Hospital, Helsinkien_US
dc.identifier.affiliationIntensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinkien_US
dc.identifier.affiliationMedical Research Institute of New Zealand and the Department of Critical Care Medicine, Auckland City Hospital, Auckland, New Zealanden_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28952891en_US
dc.identifier.doi10.1056/NEJMoa1707572en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-1650-8939en_US
dc.type.austinJournal Articleen_US
local.name.researcherBellomo, Rinaldo
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

30
checked on Oct 4, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.