Publication:
Quantitative Flow Ratio to Predict Non-Target-Vessel Events Before Planned Staged Percutaneous Coronary Intervention in Patients With Acute Coronary Syndrome.

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cris.virtualsource.author-orcid31134751-5aa4-429b-82a9-a4f94bac9190
cris.virtualsource.author-orcid881e9af4-866d-4dc8-8ffd-eb7fa0dff52d
cris.virtualsource.author-orcid101f1394-72d5-4dda-b28f-666a3dee6c70
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datacite.rightsopen.access
dc.contributor.authorBär, Sarah
dc.contributor.authorKavaliauskaite, Raminta
dc.contributor.authorOtsuka, Tatsuhiko
dc.contributor.authorUeki, Yasushi
dc.contributor.authorHäner, Jonas
dc.contributor.authorLanz, Jonas
dc.contributor.authorFürholz, Monika
dc.contributor.authorPraz, Fabien Daniel
dc.contributor.authorHunziker Munsch, Lukas Christoph
dc.contributor.authorSiontis, Georgios
dc.contributor.authorPilgrim, Thomas
dc.contributor.authorStortecky, Stefan
dc.contributor.authorLosdat, Sylvain Pierre
dc.contributor.authorWindecker, Stephan
dc.contributor.authorRäber, Lorenz
dc.date.accessioned2024-10-26T16:52:31Z
dc.date.available2024-10-26T16:52:31Z
dc.date.issued2024-01-02
dc.description.abstractBACKGROUND The optimal time point of staged percutaneous coronary intervention (PCI) among patients with acute coronary syndrome (ACS) remains a matter of debate. Quantitative flow ratio (QFR) is a novel noninvasive method to assess the hemodynamic significance of coronary stenoses. We aimed to investigate whether QFR could refine the timing of staged PCI of non-target vessels (non-TVs) on top of clinical judgment for patients with ACS. METHODS AND RESULTS For this cohort study, patients with ACS from Bern University Hospital, Switzerland, scheduled to undergo out-of-hospital non-TV staged PCI were eligible. The primary end point was the composite of non-TV myocardial infarction and urgent unplanned non-TV PCI before planned staged PCI. The association between lowest QFR per patient measured in the non-TV (from index angiogram) and the primary end point was assessed using multivariable adjusted Cox proportional hazards regressions with QFR included as linear or penalized spline (nonlinear) term. QFR was measured in 1093 of 1432 patients with ACS scheduled to undergo non-TV staged PCI. Median time to staged PCI was 28 days. The primary end point occurred in 5% of the patients. In multivariable analysis (1018 patients), there was no independent association between non-TV QFR and the primary end point (hazard ratio, 0.87 [95% CI, 0.69-1.05] per 0.1 increase; P=0.125; nonlinear P=0.648). CONCLUSIONS In selected patients with ACS scheduled to undergo staged PCI at a median of 4 weeks after index PCI, QFR did not emerge as an independent predictor of non-TV events before planned staged PCI. Thus, this study does not provide conceptual evidence that QFR is helpful to refine the timing of staged PCI on top of clinical judgment. REGISTRATION URL: https://www.clinicaltrials.gov; Unique identifier: NCT02241291.
dc.description.numberOfPages13
dc.description.sponsorshipUniversitätsklinik für Kardiologie
dc.description.sponsorshipUniversitätsklinik für Kardiologie
dc.description.sponsorshipDepartment of Clinical Research (DCR) - Statistics & Methodology (Heg)
dc.identifier.doi10.48350/191041
dc.identifier.pmid38156592
dc.identifier.publisherDOI10.1161/JAHA.123.031847
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/172940
dc.language.isoen
dc.publisherAmerican Heart Association
dc.relation.ispartofJournal of the American Heart Association
dc.relation.issn2047-9980
dc.relation.organizationDCD5A442BB15E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BE42E17DE0405C82790C4DE2
dc.subjectacute coronary syndrome multivessel disease quantitative flow ratio staged percutaneous coronary intervention
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleQuantitative Flow Ratio to Predict Non-Target-Vessel Events Before Planned Staged Percutaneous Coronary Intervention in Patients With Acute Coronary Syndrome.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.startPagee031847
oaire.citation.volume13
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationDepartment of Clinical Research (DCR) - Statistics & Methodology (Heg)
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliation2Clinical Trials Unit Bern (CTU) - Statistics & Methodology (Heg)
oairecerif.author.affiliation3Department of Clinical Research (DCR)
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unibe.date.licenseChanged2024-01-04 09:01:17
unibe.description.ispublishedpub
unibe.eprints.legacyId191041
unibe.journal.abbrevTitleJ Am Heart Assoc
unibe.refereedtrue
unibe.subtype.articlejournal

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