Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38452
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dc.contributor.authorCarrie D.en
dc.contributor.authorHagiwara N.en
dc.contributor.authorRabinowitz A.en
dc.contributor.authorPompili V.en
dc.contributor.authorStone G.W.en
dc.contributor.authorDawkins K.D.en
dc.contributor.authorAllocco D.J.en
dc.contributor.authorSaito S.en
dc.contributor.authorBouchard A.en
dc.contributor.authorKelly C.R.en
dc.contributor.authorTeirstein P.S.en
dc.contributor.authorMeredith I.T.en
dc.contributor.authorFarah B.en
dc.contributor.authorDubois C.L.en
dc.contributor.authorFeldman R.L.en
dc.contributor.authorDens J.en
dc.date.accessioned2021-05-14T13:07:11Zen
dc.date.available2021-05-14T13:07:11Zen
dc.date.copyright2017en
dc.date.created20171226en
dc.date.issued2017-12-26en
dc.identifier.citationJACC: Cardiovascular Interventions. 10 (23) (pp 2392-2400), 2017. Date of Publication: 11 Dec 2017.en
dc.identifier.issn1936-8798en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/38452en
dc.description.abstractObjectives The authors sought to evaluate the final 5-year safety and effectiveness of the platinum-chromium everolimus-eluting stent (PtCr-EES) in the randomized trial, as well as in 2 single-arm substudies that evaluated PtCr-EES in small vessels (diameter <2.5 mm; n = 94) and long lesions (24 to 34 mm; n = 102). Background In the multicenter, randomized PLATINUM (PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions), the PtCr-EES was noninferior to the cobalt-chromium everolimus-eluting stent (CoCr-EES) at 1 year in 1,530 patients undergoing percutaneous coronary intervention. Methods Patients with 1 or 2 de novo coronary artery lesions (reference vessel diameter 2.50 to 4.25 mm, length <=24 mm) were randomized 1:1 to PtCr-EES versus CoCr-EES. All patients in the substudies received PtCr-EES. The primary endpoint was target lesion failure (TLF), a composite of target vessel-related cardiac death, target vessel-related myocardial infarction, or ischemia-driven target lesion revascularization. Results In the randomized trial, the 5-year TLF rate was 9.1% for PtCr-EES and 9.3% for CoCr-EES (hazard ratio [HR]: 0.97; p = 0.87). Landmark analysis demonstrated similar TLF rates from discharge to 1 year (HR: 1.12; p = 0.70) and from 1 to 5 years (HR: 0.90; p = 0.63). There were no significant differences in the rates of cardiac death, myocardial infarction, target lesion or vessel revascularization, or stent thrombosis. PtCr-EES had 5-year TLF rates of 7.0% in small vessels and 13.6% in long lesions. Conclusions PtCr-EES demonstrated comparable safety and effectiveness to CoCr-EES through 5 years of follow-up, with low rates of stent thrombosis and other adverse events. The 5-year event rates were also acceptable in patients with small vessels and long lesions treated with PtCr-EES. (The PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions [PLATINUM]; NCT00823212; The PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions in Small Vessels [PLATINUM SV]; NCT01498692; The PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of Long De Novo Coronary Artery Lesions [PLATINUM LL]; NCT01500434)Copyright © 2017 American College of Cardiology Foundationen
dc.languageEnglishen
dc.languageenen
dc.publisherElsevier Inc. (E-mail: usjcs@elsevier.com)en
dc.relation.ispartofJACC: Cardiovascular Interventionsen
dc.titleLong-Term Safety and Efficacy of Platinum Chromium Everolimus-Eluting Stents in Coronary Artery Disease: 5-Year Results From the PLATINUM Trial.en
dc.typeArticleen
dc.type.studyortrialRandomised controlled trial-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.jcin.2017.06.070en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid29217001 [http://www.ncbi.nlm.nih.gov/pubmed/?term=29217001]en
dc.identifier.source619770827en
dc.identifier.institution(Kelly, Stone) Columbia University Medical Center/New York-Presbyterian Hospital and the Cardiovascular Research Foundation, New York, New York, United States (Teirstein) Scripps Clinic, La Jolla, California, United States (Meredith) MonashHEART, Southern Health, Monash Medical Centre, Clayton, Victoria, Australia (Farah) Clinique Pasteur-Toulouse, Toulouse, France (Dubois) University Hospital Leuven, Leuven, Belgium (Feldman) Mediquest Research at Munroe Regional Medical Center, Ocala, Florida, United States (Dens) Department of Cardiology, Ziekenhuis Oost-Limburg, Genk, Belgium (Hagiwara) Tokyo Women's Medical University Hospital, Shinjuku, Tokyo, Japan (Rabinowitz) TexSan Heart Hospital, San Antonio, Texas, United States (Carrie) Universite Paul Sabatier, Centre Hospitalier Universitaire Rangueil, Toulouse, France (Pompili) University of Nebraska Medical Center, Omaha, Nebraska, United States (Bouchard) Baptist Medical Center-Princeton, Birmingham, Alabama, United States (Saito) Shonan Kamakura General Hospital, Kanagawa, Japan (Allocco, Dawkins) Boston Scientific Corporation, Marlborough, Massachusetts, United Statesen
dc.description.addressG.W. Stone, Columbia University Medical Center, The Cardiovascular Research Foundation, 1700 Broadway, 8th Floor, New York, New York 10019, United States. E-mail: gs2184@columbia.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2018 Elsevier B.V., All rights reserved.en
dc.subect.keywordscoronary artery disease drug-eluting stent(s) percutaneous coronary intervention stent designen
dc.identifier.authoremailStone G.W.; gs2184@columbia.eduen
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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