Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25694
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dc.contributor.authorKoshy, Anoop N-
dc.contributor.authorGow, Paul J-
dc.contributor.authorTestro, Adam G-
dc.contributor.authorTeh, Andrew W-
dc.contributor.authorKo, Jefferson-
dc.contributor.authorLim, Han S-
dc.contributor.authorHan, Hui-Chen-
dc.contributor.authorWeinberg, Laurence-
dc.contributor.authorVanWagner, Lisa B-
dc.contributor.authorFarouque, Omar-
dc.date2021-01-16-
dc.date.accessioned2021-01-26T22:55:57Z-
dc.date.available2021-01-26T22:55:57Z-
dc.date.issued2021-06-
dc.identifier.citationAmerican Journal of Transplantation 2021; 21(6): 2240-2245en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25694-
dc.description.abstractIt is postulated that cardiac structural abnormalities observed in cirrhotic cardiomyopathy (CCM) contribute to the electrophysiologic abnormality of QT-interval (QTc) prolongation. We sought to evaluate whether QTc prolongation is associated with intrinsic abnormalities in cardiac structure and function that characterize CCM. Consecutive patients undergoing liver transplant work-up between 2010-2018 were included. Measures of cardiac function on stress testing including cardiac reserve and chronotropic incompetence were collected prospectively and a corrected QTc≥440ms was considered prolonged. Overall, 439 patients were included and 65.1% had a prolonged QTc. There were no differences in markers of left ventricular and atrial remodelling, or resting systolic and diastolic function across QTc groups. The proportion of patients that met the criteria for a low cardiac reserve (39.2 vs 36.6%, p=0.66) or chronotropic incompetence (18.1 vs 21.3%, p=0.52) was not different in those with a QTc≥440 vs <440 ms. Further, there was no association between QTc-prolongation and CCM by either the 2005 World College of Gastroenterology or modified 2020 Cirrhotic Cardiomyopathy Consortium criteria. Conclusion: QT-interval prolongation was not associated with structural or functional cardiac abnormalities that characterize CCM. These findings suggest that CCM and QT-interval prolongation in cirrhosis may be two separate entities with distinct pathophysiological origins.en
dc.language.isoeng-
dc.titleRelationship between QT-interval prolongation and structural abnormalities in cirrhotic cardiomyopathy: A change in the current paradigm.en
dc.typeJournal Articleen
dc.identifier.journaltitleAmerican Journal of Transplantationen
dc.identifier.affiliationDivision of Gastroenterology & Hepatology and Preventive Medicine-Epidemiology Comprehensive Transplant Center, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USAen
dc.identifier.affiliationThe University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationAnaesthesiaen
dc.identifier.affiliationCardiologyen
dc.identifier.affiliationVictorian Liver Transplant Uniten
dc.identifier.doi10.1111/ajt.16500en
dc.type.contentTexten
dc.identifier.orcid0000-0002-8741-8631en
dc.identifier.orcid0000-0002-6264-2573en
dc.identifier.pubmedid33453141-
local.name.researcherFarouque, Omar
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptCardiology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptAnaesthesia-
crisitem.author.deptCardiology-
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