Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/27768
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dc.contributor.authorSeneviratne S.en
dc.contributor.authorCameron J.en
dc.contributor.authorWong D.en
dc.contributor.authorMeredith I.en
dc.contributor.authorKo B.en
dc.contributor.authorNarayan O.en
dc.contributor.authorLeong D.en
dc.contributor.authorMalaiapan Y.en
dc.date.accessioned2021-05-14T09:21:07Zen
dc.date.available2021-05-14T09:21:07Zen
dc.date.copyright2013en
dc.date.created20150108en
dc.date.issued2015-02-02en
dc.identifier.citationHeart Lung and Circulation. Conference: Cardiac Society of Australia and New Zealand Annual Scientific Meeting and the International Society for Heart Research Australasian Section Annual Scientific Meeting 2013. Gold Coast, QLD Australia. Conference Publication: (var.pagings). 22 (SUPPL. 1) (pp S127), 2013. Date of Publication: 2013.en
dc.identifier.issn1443-9506en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/27768en
dc.description.abstractBackground: Angiographic evaluation of diameter stenosis has only modest predictive value for functionally significant coronary-artery-stenoses as assessed by fractional-flow-reserve (FFR). Lesion length and assessment of area of myocardium at risk (BAR Imyocardial- jeopardy-index) subtended by the stenotic coronary arteries are also predictors of functionally significant coronary-artery-stenoses. We compared the diagnostic accuracy of minimal-lumen-diameter (MLD), lesion length and BARI-myocardial-jeopardy-index (MJI) in prediction of significantly reduced FFR (<=0.8). Method(s): We assessed consecutive patients who underwent coronary angiography and FFR. Lesion length and MLD were assessed by QCA. Estimation of area-of myocardium at risk subtended by coronary stenoses was performed using the BARI-MJI. Coronary stenoses were classified as functionally significant when FFR was <=0.8. Result(s): One hundred and ninety-six consecutive patients (age 65.6+/-10.9; 69% male, 306 vessels) were included. 117 vessels (51%) had FFR <=0.8. The BARI MJI was 34.2+/-13.8 in vessels with FFR <=0.8 compared to 21.8+/-11.0 in vessels with FFR >0.8 (P < 0.001). The mean lesion length in vessels with FFR <=0.8 was 18.7mm vs 9.37mm in vessels with FFR >0.8 (P < 0.001). The MLD in vessels with FFR <=0.8 was 1.16+/-0.458 mm compared to 1.51+/-0.470 mm in vessels with FFR >0.8 (P < 0.001). The bootstrapped Harrell's c-statistic of BARI MJI, lesion length and MLD in predicting significant FFR were 0.76 (0.71-0.82), 0.75 (0.70-0.80) and 70 (0.65-0.75), respectively. Conclusion(s): Diameter stenosis alone has modest predictive value of significant FFR. Area of myocardium at risk and lesion length are also predictors of functionally significant coronary artery stenoses.en
dc.languageenen
dc.languageEnglishen
dc.publisherElsevier Ltden
dc.titleArea of myocardium at risk and lesion length are predictors of functionally significant coronary artery stenoses assessed by fractional flow reserve.en
dc.typeConference Abstracten
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.hlc.2013.05.303en
local.date.conferencestart2013-08-08en
dc.identifier.source71743869en
dc.identifier.institution(Wong) MonashHEART, Victoria, and Royal Adelaide Hospital, University of Adelaide, Australia (Ko, Narayan, Seneviratne, Cameron, Meredith, Malaiapan) Monash Cardiovascular Research Centre, Department of Medicine Monash University, MonashHEART, Monash Medical Centre, Australia (Leong) Flinders University, Australia (Leong) University of Adelaide, Australiaen
dc.description.addressD. Wong, MonashHEART, Victoria, and Royal Adelaide Hospital, University of Adelaide, Australiaen
dc.description.publicationstatusCONFERENCE ABSTRACTen
local.date.conferenceend2013-08-11en
dc.rights.statementCopyright 2015 Elsevier B.V., All rights reserved.en
dc.identifier.affiliationext(Wong) MonashHEART, Victoria, and Royal Adelaide Hospital, University of Adelaide, Australia-
dc.identifier.affiliationext(Leong) Flinders University, Australia-
dc.identifier.affiliationext(Leong) University of Adelaide, Australia-
dc.identifier.affiliationmh(Ko, Narayan, Seneviratne, Cameron, Meredith, Malaiapan) Monash Cardiovascular Research Centre, Department of Medicine Monash University, MonashHEART, Monash Medical Centre, Australia-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeConference Abstract-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptCardiology (MonashHeart & Victorian Heart Institute)-
crisitem.author.deptCardiology (MonashHeart & Victorian Heart Institute)-
crisitem.author.deptCardiology (MonashHeart & Victorian Heart Institute)-
crisitem.author.deptCardiology (MonashHeart & Victorian Heart Institute)-
crisitem.author.deptCardiology (MonashHeart & Victorian Heart Institute)-
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