Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16257
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dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorMårtensson, Johan-
dc.contributor.authorKaukonen, Kirsi-Maija-
dc.contributor.authorLo, Serigne-
dc.contributor.authorGallagher, Martin-
dc.contributor.authorCass, Alan-
dc.contributor.authorMyburgh, John-
dc.contributor.authorFinfer, Simon-
dc.contributor.authorRandomized Evaluation of Normal Versus Augmented Level of Replacement Therapy Study Investigators-
dc.contributor.authorAustralian and New Zealand Intensive Care Society Clinical Trials Group-
dc.date.accessioned2016-09-14T00:38:03Z-
dc.date.available2016-09-14T00:38:03Z-
dc.date.issued2016-05-
dc.identifier.citationCritical Care Medicine 2016; 44(5): 892-900en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16257-
dc.description.abstractObjective: To assess the epidemiology and outcomes associated with RBC transfusion in patients with severe acute kidney injury requiring continuous renal replacement therapy. Design: Post hoc analysis of data from a multicenter, randomized, controlled trial. Setting: Thirty-five ICUs in Australia and New Zealand. Patients: Cohort of 1,465 patients enrolled in the Randomized Evaluation of Normal versus Augmented Level replacement therapy study. Interventions: Daily information on morning hemoglobin level and amount of RBC transfused were prospectively collected in the Randomized Evaluation of Normal versus Augmented Level study. We analyzed the epidemiology of such transfusions and their association with clinical outcomes. Measurements and Main Results: Overall, 977 patients(66.7%) received a total of 1,192 RBC units. By day 5, 785 of 977 transfused patients (80.4%) had received at least one RBC transfusion. Hemoglobin at randomization was lower in transfused than in nontransfused patients (94 vs 111 g/L; p < 0.001). Mean daily hemoglobin was 88 ± 7 and 99 ± 12 g/L in transfused and nontransfused patients. Among transfused patients, 228 (46.7%) had died by day 90 when compared with 426 (43.6%) of nontransfused patients (p = 0.27). Survivors received on average 316 ± 261 mL of RBC, whereas nonsurvivors received 302 ± 362 mL (p = 0.42). On multivariate Cox regression analysis, RBC transfusion was independently associated with lower 90-day mortality (hazard ratio, 0.55; 95% CI, 0.38–0.79). However, we found no independent association between RBC transfusions and mortality when the analyses were restricted to patients surviving at least 5 days (hazard ratio, 1.29; 95% CI, 0.90–1.85). We found no independent association between RBC transfusion and renal replacement therapy–free days, mechanical ventilator–free days, or length of stay in ICU or hospital. Conclusions: In patients with severe acute kidney injury treated with continuous renal replacement therapy, we found no association of RBC transfusion with 90-day mortality or other patient-centered outcomes. The optimal hemoglobin threshold for RBC transfusion in such patients needs to be determined in future randomized controlled trials.en_US
dc.subjectAcute Kidney Injuryen_US
dc.subjectCritical Illnessen_US
dc.subjectErythrocyte Transfusionen_US
dc.subjectHemoglobinsen_US
dc.subjectRenal Replacement Therapyen_US
dc.titleEpidemiology of RBC transfusions in patients with severe acute kidney injury: analysis from the randomized evaluation of normal versus augmented level studyen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleCritical Care Medicineen_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre (ANZIC-RC), Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Intensive Care, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationSection of Anaesthesia and Intensive Care Medicine, Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Swedenen_US
dc.identifier.affiliationDepartment of Anaesthesiology, Helsinki University Central Hospital, Helsinki, Finlanden_US
dc.identifier.affiliationDepartment of Nephrology, The George Institute for Global Health, University of Sydney, Sydney, NSW, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/26619086en_US
dc.identifier.doi10.1097/CCM.0000000000001518en_US
dc.type.contentTexten_US
dc.type.austinJournal Articleen_US
local.name.researcherBellomo, Rinaldo
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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