Comparison of Contemporary Drug-eluting Coronary Stents - Is Any Stent Better than the Others?

IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Heart International Pub Date : 2020-06-18 eCollection Date: 2020-01-01 DOI:10.17925/HI.2020.14.1.34
William Parker, Javaid Iqbal
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引用次数: 6

Abstract

Percutaneous coronary intervention (PCI) with implantation of a metallic drug-eluting stent (DES) is the mainstay of treatment in patients with significant coronary artery disease or acute coronary syndromes. DESs comprise a metallic platform and an anti-proliferative drug, usually released from a polymer coating. A wide range of DESs, differing in platform, polymer or drug, are currently available for clinical use. Although there are significant differences in the physical, biological and pharmacological properties of contemporary DESs, it remains unclear whether these impact meaningfully on clinical outcomes for patients undergoing PCI. Numerous randomised clinical trials have compared DESs in recent years, but these trials are typically designed to show non-inferiority, rather than superiority. Data from meta-analyses have helped to study this in larger populations, but have limitations. Improvement in stent design continues and ongoing work is exploring the effects of new innovations as well as gathering further data on existing devices. This review explores the development, properties and clinical efficacy of current-generation DESs, comparing different types where possible, whilst identifying areas of further work.

当代药物洗脱冠状动脉支架的比较——是否有一种支架比其他支架更好?
经皮冠状动脉介入治疗(PCI)植入金属药物洗脱支架(DES)是治疗严重冠状动脉疾病或急性冠状动脉综合征患者的主要方法。DESs包括金属平台和抗增殖药物,通常从聚合物涂层中释放。目前临床使用的DESs种类繁多,平台、聚合物或药物不同。尽管当代DESs在物理、生物学和药理学特性上存在显著差异,但尚不清楚这些差异是否会对PCI患者的临床结果产生有意义的影响。近年来,许多随机临床试验对DESs进行了比较,但这些试验通常旨在显示非劣效性,而不是优越性。荟萃分析的数据有助于在更大的人群中研究这一点,但有局限性。支架设计的改进仍在继续,正在进行的工作是探索新的创新的影响,以及收集现有设备的进一步数据。这篇综述探讨了当前一代DESs的发展、特性和临床疗效,比较了不同类型的DESs,同时确定了进一步工作的领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Heart International
Heart International Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.90
自引率
0.00%
发文量
9
审稿时长
7 weeks
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