Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16877
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dc.contributor.authorLloyd-Donald, Patryck-
dc.contributor.authorVasudevan, Abhinav-
dc.contributor.authorAngus, Peter W-
dc.contributor.authorGow, Paul J-
dc.contributor.authorMårtensson, Johan-
dc.contributor.authorGlassford, Neil J-
dc.contributor.authorEastwood, Glenn M-
dc.contributor.authorHart, Graeme K-
dc.contributor.authorBellomo, Rinaldo-
dc.date2016-11-04-
dc.date.accessioned2017-09-26T23:39:01Z-
dc.date.available2017-09-26T23:39:01Z-
dc.date.issued2017-04-
dc.identifier.citationJournal of Critical Care 2017; 38: 215-224en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16877-
dc.description.abstractBackground and aims There is controversy about the true coagulation state of acutely ill patients with chronic liver disease (CLD) due to simultaneous pro- and anticoagulant factor deficits and limitations of conventional coagulation tests (CCTs). Thromboelastography (TEG) may provide more physiologically relevant insights. Methods In acutely ill patients with severe (Child-Pugh C) CLD, we conducted a prospective observational study of daily coagulation assessment with both CCTs and TEG. Results We studied 34 patients with CLD on a total of 109 occasions (median of 3 samples per patient), comparing findings with 157 healthy controls. Conventional coagulation tests and TEG both demonstrated clear hypocoagulability. Thromboelastography-confirmed delayed clot formation was demonstrated by longer reaction time (1.1 minutes vs 0.6 minutes on rapid TEG; P < .01), longer kinetic time (2.9 minutes vs 1.3; P < .01), more acute α angle (65° vs 72.2°; P < .01), and longer activated clotting time (157 seconds vs 105 seconds; P < .01). Patients with CLD demonstrated weaker thrombus strength (maximum amplitude, 43.3 mm vs 61.8 mm; P < .01) and reduced clot lysis (0% vs 1% on rapid TEG; P < .01). Conclusions In acutely ill patients with CLD, TEG demonstrates delayed clot formation and weaker thrombus strength despite decreased clot lysis. This challenges the notion that such patients experience a balanced coagulation state, highlighting the complexity of their coagulopathies.en_US
dc.subjectHepatic cirrhosisen_US
dc.subjectGlobal coagulation assaysen_US
dc.subjectThromboelastographyen_US
dc.subjectCoagulopathyen_US
dc.titleCoagulation in acutely ill patients with severe chronic liver disease: insights from thromboelastographyen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Critical Careen_US
dc.identifier.affiliationIntensive Careen_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationDepartment of Anesthesia and Intensive Care Medicine, Karolinska University Hospital, Solna, Swedenen_US
dc.identifier.affiliationDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Swedenen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/27978499en_US
dc.identifier.doi10.1016/j.jcrc.2016.10.030en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-1650-8939en_US
dc.type.austinJournal Articleen_US
local.name.researcherAngus, Peter W
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptIntensive Care-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptIntensive Care-
crisitem.author.deptIntensive Care-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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