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dc.contributor.authorBär, S
dc.contributor.authorKavaliauskaite, R
dc.contributor.authorUeki, Y
dc.contributor.authorOtsuka, T
dc.contributor.authorKelbæk, H
dc.contributor.authorEngstrøm, T
dc.contributor.authorBaumbach, A
dc.contributor.authorRoffi, M
dc.contributor.authorvon Birgelen, C
dc.contributor.authorOstojic, M
dc.contributor.authorPedrazzini, G
dc.contributor.authorKornowski, R
dc.contributor.authorTüller, D
dc.contributor.authorVukcevic, V
dc.contributor.authorMagro, M
dc.contributor.authorLosdat, S
dc.contributor.authorWindecker, S
dc.contributor.authorRäber, L
dc.date.accessioned2021-08-02T17:58:41Z
dc.date.available2021-08-02T17:58:41Z
dc.date.issued2021-05-04
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/73381
dc.description.abstractBackground In ST-segment-elevation myocardial infarction, angiography-based complete revascularization is superior to culprit-lesion-only percutaneous coronary intervention. Quantitative flow ratio (QFR) is a novel, noninvasive, vasodilator-free method used to assess the hemodynamic significance of coronary stenoses. We aimed to investigate the incremental value of QFR over angiography in nonculprit lesions in patients with ST-segment-elevation myocardial infarction undergoing angiography-guided complete revascularization. Methods and Results This was a retrospective post hoc QFR analysis of untreated nontarget vessels (any degree of diameter stenosis [DS]) from the randomized multicenter COMFORTABLE AMI (Comparison of Biolimus Eluted From an Erodible Stent Coating With Bare Metal Stents in Acute ST-Elevation Myocardial Infarction) trial by assessors blinded for clinical outcomes. The primary end point was cardiac death, spontaneous nontarget vessel myocardial infarction, and clinically indicated nontarget vessel revascularization (ie, ≥70% DS by 2-dimensional quantitative coronary angiography or ≥50% DS and ischemia) at 5 years. Of 1161 patients with ST-segment-elevation myocardial infarction, 946 vessels in 617 patients were analyzable by QFR. At 5 years, the rate of the primary end point was significantly higher in patients with QFR ≤0.80 (n=35 patients, n=36 vessels) versus QFR >0.80 (n=582 patients, n=910 vessels) (62.9% versus 12.5%, respectively; hazard ratio [HR], 7.33 [95% CI, 4.54-11.83], P<0.001), driven by higher rates of nontarget vessel myocardial infarction (12.8% versus 3.1%, respectively; HR, 4.38 [95% CI, 1.47-13.02], P=0.008) and nontarget vessel revascularization (58.6% versus 7.7%, respectively; HR, 10.99 [95% CI, 6.39-18.91], P<0.001) with no significant differences for cardiac death. Multivariable analysis identified QFR ≤0.80 but not ≥50% DS by 3-dimensional quantitative coronary angiography as an independent predictor of the primary end point. Results were consistent, including only >30% DS by 3-dimensional quantitative coronary angiography. Conclusions Our study suggests incremental value of QFR over angiography-guided percutaneous coronary intervention for nonculprit lesions among patients with ST-segment-elevation myocardial infarction undergoing primary percutaneous coronary intervention.en_US
dc.format.extente019052 - ?
dc.languageeng
dc.relation.ispartofJournal of the American Heart Association
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs License
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectST‐segment–elevation myocardial infarctionen_US
dc.subjectangiographyen_US
dc.subjectcoronary flowen_US
dc.subjectfractional flow reserveen_US
dc.titleQuantitative Flow Ratio to Predict Nontarget Vessel-Related Events at 5 Years in Patients With ST-Segment-Elevation Myocardial Infarction Undergoing Angiography-Guided Revascularization.en_US
dc.typeArticleen_US
dc.rights.holder© 2021 The Authors.
dc.identifier.doi10.1161/JAHA.120.019052
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33899509en_US
pubs.issue9en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.publisher-urlhttps://doi.org/10.1161/JAHA.120.019052
pubs.volume10en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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