| Literature DB >> 33439454 |
Shoichi Kuramitsu1, Shinjo Sonoda2, Kenji Ando3, Hiromasa Otake4, Masahiro Natsuaki5, Reo Anai2, Yasuhiro Honda6, Kazushige Kadota7, Yoshio Kobayashi8, Takeshi Kimura9.
Abstract
Over the past 40 years, the safety and efficacy of percutaneous coronary intervention has dramatically improved by overcoming several challenges. The introduction of drug-eluting stent (DES) in particular was a major breakthrough in interventional cardiology. Compared to bare-metal stents, first-generation DES (G1-DES) has dramatically reduced the rates of in-stent restenosis and subsequent target lesion revascularization. However, major safety concerns surrounding stent thrombosis (ST) emerged with G1-DES in clinical practice as a result of the high incidences of death, myocardial infarction, and repeat revascularization associated with ST. To overcome these limitations, second-generation DES (G2-DES) has been developed with an improved stent platform with thinner strut and biocompatible durable or biodegradable polymers. Indeed, G2-DES, when compared with G1-DES, has improved clinical outcomes by reducing the risk of late thrombotic events while maintaining anti-restenotic efficacy, whereas ST still occurs, even with the use of G2-DES. This review gives an overview of pathophysiology, risk factors, and outcomes of ST after DES implantation. Additionally, we discuss the management and prevention of ST.Entities:
Keywords: Drug-eluting stent; Percutaneous coronary intervention; Stent thrombosis
Mesh:
Year: 2021 PMID: 33439454 DOI: 10.1007/s12928-021-00754-x
Source DB: PubMed Journal: Cardiovasc Interv Ther ISSN: 1868-4297