Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20092
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dc.contributor.authorMagne, Julien-
dc.contributor.authorCosyns, Bernard-
dc.contributor.authorPopescu, Bogdan A-
dc.contributor.authorCarstensen, Helle G-
dc.contributor.authorDahl, Jordi-
dc.contributor.authorDesai, Milind Y-
dc.contributor.authorKearney, Leighton G-
dc.contributor.authorLancellotti, Patrizio-
dc.contributor.authorMarwick, Thomas H-
dc.contributor.authorSato, Kimi-
dc.contributor.authorTakeuchi, Masaaki-
dc.contributor.authorZito, Concetta-
dc.contributor.authorCasalta, Anne-Claire-
dc.contributor.authorMohty, Dania-
dc.contributor.authorPiérard, Luc-
dc.contributor.authorHabib, Gilbert-
dc.contributor.authorDonal, Erwan-
dc.date.accessioned2019-01-18T04:19:40Z-
dc.date.available2019-01-18T04:19:40Z-
dc.date.issued2019-01-
dc.identifier.citationJACC. Cardiovascular Imaging 2019; 12(1): 84-92en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20092-
dc.description.abstractIn this individual participant data meta-analysis on left ventricular global longitudinal strain (LVGLS), our objective was to: 1) describe its distribution; 2) identify the most predictive cutoff values; and 3) assess its impact on mortality in asymptomatic patients with significant aortic stenosis (AS) and preserved left ventricular ejection fraction (LVEF). The evidence supporting the prognostic role of LVGLS in asymptomatic patients with AS has been obtained from several relatively small studies. A literature search was performed for studies published between 2005 and 2017 without language restriction according to the following criteria: "aortic stenosis" AND "longitudinal strain." The corresponding authors of selected studies were contacted and invited to share their data that we computerized in a specific database. The primary endpoint was all-cause mortality. Among the 10 studies included, 1,067 asymptomatic patients with significant AS and LVEF >50% were analyzed. The median of LVGLS was 16.2% (from 5.6% to 30.1%). There were 91 deaths reported during follow-up with median of 1.8 (0.9 to 2.8) years, resulting in a pooled crude mortality rate of 8.5%. The LVGLS performed well in the prediction of death (area under the curve: 0.68). The best cutoff value identified was LVGLS of 14.7% (sensitivity, 60%; specificity, 70%). Using random effects model, the risk of death for patients with LVGLS <14.7% is multiplied by >2.5 (hazard ratio: 2.62; 95% confidence interval: 1.66 to 4.13; p < 0.0001), without significant heterogeneity between studies (I2 = 18.3%; p = 0.275). The relationship between LVGLS and mortality remained significant in patients with LVEF ≥60% (p = 0.001). This individual participant data meta-analysis demonstrates that in asymptomatic patients with significant AS and normal LVEF, impaired LVGLS is associated with reduced survival. These data emphasize the potential usefulness of LVGLS for risk stratification and management of these patients.en_US
dc.language.isoeng-
dc.subjectaortic valve stenosisen_US
dc.subjectleft ventricular global longitudinal strainen_US
dc.subjectmeta-analysisen_US
dc.subjectmortalityen_US
dc.titleDistribution and Prognostic Significance of Left Ventricular Global Longitudinal Strain in Asymptomatic Significant Aortic Stenosis: An Individual Participant Data Meta-Analysis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJACC. Cardiovascular Imagingen_US
dc.identifier.affiliationCardiologyen_US
dc.identifier.affiliationUZ Brussel-CVHZ, Brussels, Belgiumen_US
dc.identifier.affiliationCardiology Unit, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italyen_US
dc.identifier.affiliationBaker Heart and Diabetes Institute, Melbourne, Australiaen_US
dc.identifier.affiliationCHU Limoges, Hôpital Dupuytren, Service Cardiologie, INSERM 1094, Limoges, Franceen_US
dc.identifier.affiliationUniversity of Medicine and Pharmacy "Carol Davila"-Euroecolab, Institute of Cardiovascular Diseases "Prof. Dr. C. C. Iliescu," Bucharest, Romaniaen_US
dc.identifier.affiliationDepartment of Cardiology, Gentofte Hospital, University of Copenhagen, Copenhagen, Denmarken_US
dc.identifier.affiliationDepartment of Cardiology, Odense University Hospital, Odense, Denmarken_US
dc.identifier.affiliationHeart and Vascular Institute, Cleveland Clinic, Cleveland, Ohioen_US
dc.identifier.affiliationUniversity of Liège Hospital, GIGA Cardiovascular Sciences, Department of Cardiology, CHU Sart Tilman, Liège, Belgiumen_US
dc.identifier.affiliationDepartment of Cardiology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japanen_US
dc.identifier.affiliationDepartment of Laboratory and Transfusion Medicine, Hopital of University of Occupational and Environmental Health, School of Medicine, Kitakyushu, Japanen_US
dc.identifier.affiliationDepartment of Cardiology, Gentofte Hospital, University of Copenhagen, Copenhagen, Denmarken_US
dc.identifier.affiliationCHU Limoges, Hôpital Dupuytren, Service Cardiologie, INSERM 1094, Limoges, Franceen_US
dc.identifier.affiliationUniversity of Liège Hospital, GIGA Cardiovascular Sciences, Department of Cardiology, CHU Sart Tilman, Liège, Belgiumen_US
dc.identifier.affiliationAix-Marseille Université, APHM, La Timone Hospital, Cardiology Department, Marseille, Franceen_US
dc.identifier.affiliationCardiologie et CIC-IT 1414, CHU Rennes; LTSI, Inserm 1099, University Rennes 1, Rennes, Franceen_US
dc.identifier.affiliationGruppo Villa Maria Care and Research, Anthea, Bari, Italyen_US
dc.identifier.doi10.1016/j.jcmg.2018.11.005en_US
dc.type.contentTexten_US
dc.identifier.pubmedid30621997-
dc.type.austinJournal Article-
local.name.researcherKearney, Leighton G
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptCardiology-
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