Department of Cardiovascular Sciences, European Hospital, Rome, Italy.
Catheter Cardiovasc Interv. 2015 Feb 15;85(3):352-8. doi: 10.1002/ccd.25627. Epub 2014 Aug 28.
To evaluate the performance of biolimus-eluting stent (BES) in patients with ST-elevation myocardial infarction (STEMI) undergoing percutaneous coronary intervention (PCI) in a real world clinical scenario.
Randomized studies suggest that the BES with biodegradable polymer is more effective and safe than early generation coronary stents in patients with STEMI.
We included all consecutive STEMI patients undergoing PCI in this prospective, multicenter registry. The primary endpoint of the study was the rate of major adverse cardiac events (MACE), a composite of cardiac death, recurrent myocardial infarction and ischemia-driven target vessel revascularization at 1-year follow-up.
Between June and December 2012 we enrolled 311 STEMI patients. The primary endpoint occurred in 3.2% (95% confidence interval: 1.6-5.8) of patients: cardiac death, re-infarction, and ischemia-driven TVR occurred in 2.3%, 1.3%, and 0.6% of patients, respectively. One-year MACE-free survival was 96.8% ± 1.0%.
In a real-world cohort of STEMI patients undergoing PCI, the use of BES is associated with good 1-year clinical outcome. These results confirm and expand previous findings showing the efficacy and safety of BES in the setting of randomized trials.
评估生物可降解聚合物涂层雷帕霉素洗脱支架(BES)在经皮冠状动脉介入治疗(PCI)治疗 ST 段抬高型心肌梗死(STEMI)患者中的临床疗效。
随机研究表明,在 STEMI 患者中,与早期冠状动脉支架相比,BES 具有更好的有效性和安全性。
我们纳入了这项前瞻性、多中心注册研究中所有连续接受 PCI 的 STEMI 患者。研究的主要终点是 1 年随访时主要不良心脏事件(MACE)的发生率,MACE 是心脏死亡、再发心肌梗死和缺血驱动的靶血管血运重建的复合终点。
2012 年 6 月至 12 月期间,我们共纳入了 311 例 STEMI 患者。主要终点事件发生率为 3.2%(95%置信区间:1.6-5.8):心脏死亡、再梗死和缺血驱动的 TVR 分别占 2.3%、1.3%和 0.6%。1 年 MACE 无事件生存率为 96.8%±1.0%。
在接受 PCI 的 STEMI 患者的真实世界队列中,BES 的使用与良好的 1 年临床结局相关。这些结果证实并扩展了先前在随机试验中显示 BES 的疗效和安全性的发现。