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Drug-eluting stents to prevent stent thrombosis and restenosis

DC Field Value Language
dc.contributor.author임의-
dc.contributor.author홍명기-
dc.date.accessioned2017-01-19T12:57:55Z-
dc.date.available2017-01-19T12:57:55Z-
dc.date.issued2016-
dc.identifier.issn1477-9072-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/145509-
dc.description.abstractAlthough first-generation drug-eluting stents (DES) have significantly reduced the risk of in-stent restenosis, they have also increased the long-term risk of stent thrombosis. This safety concern directly triggered the development of new generation DES, with innovations in stent platforms, polymers, and anti-proliferative drugs. Stent platform materials have evolved from stainless steel to cobalt or platinum-chromium alloys with an improved strut design. Drug-carrying polymers have become biocompatible or biodegradable and even polymer-free DES were introduced. New limus-family drugs (such as everolimus, zotarolimus or biolimus) were adopted to enhance stent performances. As a result, these new DES demonstrated superior vascular healing responses on intracoronary imaging studies and lower stent thrombotic events in actual patients. Recently, fully-bioresorbable stents (scaffolds) have been introduced, and expanding their applications. In this article, the important concepts and clinical results of new generation DES and bioresorbable scaffolds are described.-
dc.description.statementOfResponsibilityrestriction-
dc.format.extent87~104-
dc.languageEnglish-
dc.publisherTaylor & Francis-
dc.relation.isPartOfEXPERT REVIEW OF CARDIOVASCULAR THERAPY-
dc.subject.MESHAbsorbable Implants-
dc.subject.MESHCoated Materials, Biocompatible/pharmacology-
dc.subject.MESHCoronary Restenosis*/etiology-
dc.subject.MESHCoronary Restenosis*/prevention & control-
dc.subject.MESHDrug-Eluting Stents*/adverse effects-
dc.subject.MESHDrug-Eluting Stents*/standards-
dc.subject.MESHHumans-
dc.subject.MESHImmunosuppressive Agents/pharmacology-
dc.subject.MESHInventions-
dc.subject.MESHPercutaneous Coronary Intervention/instrumentation*-
dc.subject.MESHPolymers/pharmacology-
dc.subject.MESHPostoperative Complications/prevention & control*-
dc.subject.MESHRandomized Controlled Trials as Topic-
dc.subject.MESHSirolimus*/analogs & derivatives-
dc.subject.MESHSirolimus*/pharmacology-
dc.subject.MESHThrombosis*/etiology-
dc.subject.MESHThrombosis*/prevention & control-
dc.titleDrug-eluting stents to prevent stent thrombosis and restenosis-
dc.typeArticle-
dc.publisher.locationEngland-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Internal Medicine-
dc.contributor.googleauthorEui Im-
dc.contributor.googleauthorMyeong-Ki Hong-
dc.identifier.doi10.1586/14779072.2016.1112267-
dc.contributor.localIdA03394-
dc.contributor.localIdA04391-
dc.relation.journalcodeJ00879-
dc.identifier.eissn1744-8344-
dc.identifier.pmid26567863-
dc.identifier.urlhttp://www.tandfonline.com/doi/full/10.1586/14779072.2016.1112267-
dc.subject.keyworddrug-eluting stent-
dc.subject.keywordstent restenosis-
dc.subject.keywordstent thrombosis-
dc.contributor.alternativeNameIm, Eui-
dc.contributor.alternativeNameHong, Myeong Ki-
dc.contributor.affiliatedAuthorIm, Eui-
dc.contributor.affiliatedAuthorHong, Myeong Ki-
dc.citation.volume14-
dc.citation.number1-
dc.citation.startPage87-
dc.citation.endPage104-
dc.identifier.bibliographicCitationEXPERT REVIEW OF CARDIOVASCULAR THERAPY, Vol.14(1) : 87-104, 2016-
dc.date.modified2017-01-16-
dc.identifier.rimsid47365-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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