Suppr超能文献

Endeavor 佐他莫司洗脱支架临床试验项目的 5 年最终结果:与第一代药物洗脱支架和裸金属支架的安全性和疗效比较。

Final 5-year outcomes from the Endeavor zotarolimus-eluting stent clinical trial program: comparison of safety and efficacy with first-generation drug-eluting and bare-metal stents.

机构信息

Piedmont Heart Institute, Atlanta, Georgia 30309, USA.

出版信息

JACC Cardiovasc Interv. 2013 May;6(5):504-12. doi: 10.1016/j.jcin.2012.12.125. Epub 2013 Apr 17.

Abstract

OBJECTIVES

The aim of this study was to evaluate late safety and efficacy outcomes among patients enrolled in clinical trials comparing Endeavor zotarolimus-eluting stents (E-ZES) (Medtronic, Inc., Santa Rosa, California) with first-generation drug-eluting stents (DES) and bare-metal stents (BMS).

BACKGROUND

Despite demonstration of higher angiographic luminal loss and restenosis with E-ZES compared with alternative DES, whether differences in these early angiographic measures translate into more disparate late clinical events is uncertain.

METHODS

Among 3,616 patients undergoing percutaneous coronary revascularization in 5 registration trials, late safety and efficacy events were compared between E-ZES (n = 2,132) versus sirolimus- or paclitaxel-eluting stents (n = 888) or BMS (n = 596).

RESULTS

Compared with a parallel cohort of patients treated with first-generation DES and BMS, 5-year rates of cardiac death/myocardial infarction (MI) (5.8% vs. 8.8% DES, p = 0.003; vs. 8.4% BMS, p = 0.02) and major adverse cardiac events (16.1% vs. 20.6% DES, p = 0.009; vs. 24.6% BMS, p < 0.001) were significantly lower with E-ZES. The E-ZES was associated with significantly lower target lesion revascularization (TLR) compared with BMS (7.4% vs. 16.3%, p < 0.001) but similar to comparator DES (7.4% vs. 8.1%, p = 0.63). Despite higher TLR in the first year with E-ZES compared with DES, between 1- and 5-year follow-up, rates of cardiac death/MI, TLR, and definite/probable stent thrombosis were significantly lower with E-ZES.

CONCLUSIONS

Over 5 years, significant differences in cardiac death/MI and composite endpoints favored treatment with E-ZES over comparator BMS and DES. Rates of clinical restenosis and safety events, including stent thrombosis beyond the first year of revascularization, remain stable with E-ZES, leading to significant differences compared with first-generation DES.

摘要

目的

本研究旨在评估对比 Endeavor 佐他莫司洗脱支架(E-ZES)(美敦力公司,加利福尼亚州圣罗莎)与第一代药物洗脱支架(DES)和裸金属支架(BMS)的临床试验中入组患者的晚期安全性和疗效结局。

背景

尽管与其他 DES 相比,E-ZES 显示出更高的血管造影管腔丢失和再狭窄,但这些早期血管造影测量结果是否转化为更不同的晚期临床事件尚不确定。

方法

在 5 项注册试验中,有 3616 名接受经皮冠状动脉血运重建的患者,比较 E-ZES(n=2132)与西罗莫司或紫杉醇洗脱支架(n=888)或 BMS(n=596)之间的晚期安全性和疗效事件。

结果

与接受第一代 DES 和 BMS 治疗的平行队列患者相比,E-ZES 组 5 年时的心脏死亡/心肌梗死(MI)(5.8%比 DES 组 8.8%,p=0.003;比 BMS 组 8.4%,p=0.02)和主要不良心脏事件(16.1%比 DES 组 20.6%,p=0.009;比 BMS 组 24.6%,p<0.001)发生率显著降低。E-ZES 与 BMS 相比,靶病变血运重建(TLR)发生率显著降低(7.4%比 16.3%,p<0.001),但与对照 DES 相似(7.4%比 8.1%,p=0.63)。尽管 E-ZES 在前 1 年的 TLR 高于 DES,但在 1 至 5 年的随访期间,E-ZES 组的心脏死亡/MI、TLR 和确定/可能的支架血栓形成的发生率显著降低。

结论

在 5 年期间,E-ZES 在心脏死亡/MI 和复合终点方面与对照 BMS 和 DES 相比具有显著差异。E-ZES 的临床再狭窄和安全性事件(包括血运重建后第一年的支架血栓形成)发生率保持稳定,与第一代 DES 相比,E-ZES 具有显著差异。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验