Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/27989
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dc.contributor.authorWong D.en
dc.contributor.authorCameron J.en
dc.contributor.authorMalaiapan Y.en
dc.contributor.authorSeneviratne S.en
dc.contributor.authorMeredith I.T.en
dc.contributor.authorNarayan O.en
dc.contributor.authorKo B.S.en
dc.contributor.authorLeong D.en
dc.date.accessioned2021-05-14T09:25:37Zen
dc.date.available2021-05-14T09:25:37Zen
dc.date.copyright2013en
dc.date.created20131121en
dc.date.issued2013-11-26en
dc.identifier.citationJournal of the American College of Cardiology. Conference: 25th Annual Symposium Transcatheter Cardiovascular Therapeutics, TCT 2013. San Francisco, CA United States. Conference Publication: (var.pagings). 62 (18 SUPPL. 1) (pp B189), 2013. Date of Publication: 29 Oct 2013.en
dc.identifier.issn0735-1097en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/27989en
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 (BARI-myocardial-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 areaof- 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): 196 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 18.7 vs 9.37 mm 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 USAen
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.jacc.2013.08.1371en
local.date.conferencestart2013-10-27en
dc.identifier.source71228674en
dc.identifier.institution(Wong, Cameron, Seneviratne) Monash Heart, Clayton, VIC, Australia (Narayan, Ko) Monash Heart, Monash Cardiovascular Research Centre, Clayton, VIC, Australia (Leong) Leiden University, Medical Centre, Wassenaar, Leiden, Netherlands (Meredith) Monash University, Melbourne, Australia (Malaiapan) Monash Medical Centre, Clayton, VIC, Australiaen
dc.description.addressD. Wong, Monash Heart, Clayton, VIC, Australiaen
dc.description.publicationstatusCONFERENCE ABSTRACTen
local.date.conferenceend2013-11-01en
dc.rights.statementCopyright 2013 Elsevier B.V., All rights reserved.en
dc.identifier.affiliationext(Leong) Leiden University, Medical Centre, Wassenaar, Leiden, Netherlands-
dc.identifier.affiliationext(Meredith) Monash University, Melbourne, Australia-
dc.identifier.affiliationmh(Wong, Cameron, Seneviratne) Monash Heart, Clayton, VIC, Australia-
dc.identifier.affiliationmh(Narayan, Ko) Monash Heart, Monash Cardiovascular Research Centre, Clayton, VIC, Australia-
dc.identifier.affiliationmh(Malaiapan) Monash Medical Centre, Clayton, VIC, 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)-
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