| Literature DB >> 27665404 |
Ming-Lung Tsai1, Chun-Chi Chen1, Dong-Yi Chen1, Chia-Hung Yang1, Ming-Jer Hsieh1, Cheng-Hung Lee1, Chao-Yung Wang1, Shang-Hung Chang1, I-Chang Hsieh2.
Abstract
Compared to bare metal stent (BMS) implantation, drug-eluting stents (DES) is significantly better in attenuating intimal hyperplasia and reducing the rate of revascularization. However, the requirement of prolonged dual antiplatelet therapy (DAPT) and the economic cost have been the major disadvantages of DES. Studies have shown that the use of DES in small vessels decrease revascularization rate, but the results in large vessels vary. Previous studies have shown that the extent of late loss is unrelated to vessel diameter, and that late loss is easily accommodated in large vessels, thus resulting in decreased clinical benefit of DES in this setting. No definite cut-off point value of the vessel size has yet been demonstrated. Series studies aimed at evaluating the clinical outcomes of DES versus BMS in large vessels, but their results have been controversial. In this review, we evaluate the latest studies on clinical outcomes for different vessel sizes and clinical conditions. Nonetheless, further large clinical trials are warranted to address the clinical results of newer stents in different size vessels, especially in large vessels.Entities:
Keywords: Bare metal stent; Coronary Artery Disease; Drug eluting stent; Stent
Mesh:
Substances:
Year: 2016 PMID: 27665404 DOI: 10.1016/j.ijcard.2016.09.061
Source DB: PubMed Journal: Int J Cardiol ISSN: 0167-5273 Impact factor: 4.164