Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38496
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dc.contributor.authorVan Geuns R.-J.en
dc.contributor.authorDe Bruyne B.en
dc.contributor.authorChristiansen E.en
dc.contributor.authorKoolen J.en
dc.contributor.authorSmits P.en
dc.contributor.authorChevalier B.en
dc.contributor.authorMcClean D.en
dc.contributor.authorDudek D.en
dc.contributor.authorWindecker S.en
dc.contributor.authorMeredith I.en
dc.contributor.authorNieman K.en
dc.contributor.authorVeldhof S.en
dc.contributor.authorOrmiston J.en
dc.contributor.authorSerruys P.W.en
dc.contributor.authorOnuma Y.en
dc.contributor.authorCollet C.en
dc.date.accessioned2021-05-14T13:08:06Zen
dc.date.available2021-05-14T13:08:06Zen
dc.date.copyright2017en
dc.date.created20171226en
dc.date.issued2017-12-26en
dc.identifier.citationEuropean Heart Journal Cardiovascular Imaging. 18 (8) (pp 870-879), 2017. Date of Publication: 01 Aug 2017.en
dc.identifier.issn2047-2404en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/38496en
dc.description.abstractAims Multimodality invasive imaging of the first-in-man cohort demonstrated at 5 years stable lumen dimensions and a low rate of major adverse cardiac events (MACE). However, the long-term non-invasive assessment of this device remains to be documented. The objective was to describe the 72-month multislice computed tomography (MSCT) angiographic and functional findings after the implantation of the second iteration of the fully resorbable everolimus-eluting polymeric scaffold. Methods and results In the ABSORB Cohort B trial patients with non-complex de novo lesions were treated with second iteration bioresobable vascular scaffold (BVS). MSCT angiography was performed as an optional investigation at 18 months; patients were reconsented for a second investigation at 72 months. MSCT data were analysed at independent core laboratories for quantitative analysis of lumen dimensions and for calculation of fractional flow reserve derived from computed tomography (FFRCT). From the overall Cohort B (101 patients), 53 patients underwent MSCT imaging at 72 months. The MACE rate was 1.9% (1/53). At 72 months, the median minimal lumen area (MLA) was 4.05 mm2 (interquartile range [IQR]: 3.15-4.90) and the mean percentage area stenosis was 18% (IQR: 4.75-31.25), one scaffold was totally occluded. In 39 patients with paired MSCT analysis, the MLA significantly increased from the first to the second follow-up (delta = 0.80 mm2, P = 0.002). The change in the median FFRCT scaffold gradient between time points was zero. Conclusion The long-term serial non-invasive MSCT evaluation with FFRCT assessment after bioresorbable scaffold implantation confirmed in-scaffold late lumen enlargement with the persistence of normalization of the FFRCT. Clinical trial URL: http://www.clinicaltrials.gov. Unique identifier: NCT00856856.Copyright © 2017 The Author.en
dc.languageenen
dc.languageEnglishen
dc.publisherOxford University Pressen
dc.relation.ispartofEuropean Heart Journal Cardiovascular Imagingen
dc.titleLong-term serial non-invasive multislice computed tomography angiography with functional evaluation after coronary implantation of a bioresorbable everolimus-eluting scaffold: The ABSORB cohort B MSCT substudy.en
dc.typeArticleen
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1093/ehjci/jex022en
dc.publisher.placeUnited Kingdomen
dc.identifier.pubmedid28329198 [http://www.ncbi.nlm.nih.gov/pubmed/?term=28329198]en
dc.identifier.source619714424en
dc.identifier.institution(Onuma, Van Geuns, Nieman) Department of Interventional Cardiology, ThoraxCenter, Erasmus University Medical Center, s-Gravendijkwal 230, CE Rotterdam 3015, Netherlands (Onuma, Nieman) Cardiology Department, Academic Medical Center, Meibergdreef 9, AZ Amsterdam-Zuidoost, Amsterdam 1105, Netherlands (Collet) Cardiology Department, Academic Medical Center, Westblaak 98, KM Rotterdam 3012, Netherlands (De Bruyne) Department of Cardiology, Onze-Lieve-Vrouwziekenhuis, Moorselbaan 164, Aalst 9300, Belgium (Christiansen) Department of Cardiology, Skejby Sygehus, Aarhus Universitet Skejby Sygehus, Brendstrupgardsvej 100, Aarhus N 8200, Denmark (Koolen) Department of Cardiology, Catharina Ziekenhuis, Michelangelolaan 2, EJ Eindhoven 5623, Netherlands (Smits) Department of Cardiology, Maasstad Ziekenhuis, Maasstadweg 21, DZ, Rotterdam 3079, Netherlands (Chevalier) Department of Interventional Cardiology, Institut Hospital Jacques Cartier, 6 Avenue du Noyer Lambert, Massy 91300, France (McClean) Department of Cardiology, Christchurch Hospital, Christchurch Central, 2 Riccarton Ave, Christchurch 4710, New Zealand (Dudek) Jagiellonian University Institute of Cardiology, University Hospital Krakow, Mikolaja Kopernika 36, Krakow 31-501, Poland (Windecker) Universit Atsklinik Fur Kardiologie, Inselspital, Freiburgstrasse 4, Bern 3010, Switzerland (Meredith) Monash Heart, Monash Medical Centre, 246 Clayton Rd, Clayton, Melbourne, VIC 3168, Australia (Veldhof) Clinical Development, Abbott Vascular, Diegem, Belgium (Ormiston) Department of Cardiology, Auckland City Hospital, 2 Park Rd, Grafton, Auckland 1023, New Zealand (Serruys) Imperial College London Kensington, London SW7 2AZ, United Kingdomen
dc.description.addressP.W. Serruys, Imperial College London Kensington, London SW7 2AZ, United Kingdom. E-mail: patrick.w.j.c.serruys@pwserruys.comen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2018 Elsevier B.V., All rights reserved.en
dc.subect.keywordsCoronary computed tomography angiography Fractional flow reserve derived from computed tomography Scaffolden
dc.identifier.authoremailSerruys P.W.; patrick.w.j.c.serruys@pwserruys.comen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.deptCardiology (MonashHeart & Victorian Heart Institute)-
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