Sgueglia Gregory A, D'Errico Fabrizio, Gioffrè Gaetano, De Santis Antonella, Summaria Francesco, Piccioni Fabiana, Gaspardone Achille
Sant'Eugenio Hospital, Rome, Italy.
Catheter Cardiovasc Interv. 2018 Apr 1;91(5):851-858. doi: 10.1002/ccd.27206. Epub 2017 Aug 2.
This study aimed at assessing the performance of a new generation polymer-free biolimus-eluting stent (BES) in real-world patients with ST-segment elevation myocardial infarction (STEMI).
Polymers components of early-generation drug-eluting stents have been implicated in the pathogenesis of delayed arterial healing, vessel remodeling, and delayed stent thrombosis. Recently, a novel polymer-free BES has shown excellent clinical performance in clinical trial setting.
Overall, 175 consecutive patients (64 ± 14 years, 141 men) treated with the BioFreedom (Biosensors Europe, Morges, Switzerland) polymer-free BES because of STEMI were included in this study. The primary endpoint 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. A subgroup of patients underwent 6-month angiographic follow-up. Dual antiplatelet therapy was prescribed for 12 months after STEMI.
At 1 year, the cumulative rate of MACE was 4.6%. One patient (0.6%) had an arrhythmic cardiac death and five (2.9%) had ischemia-driven target vessel revascularization, although only three (1.7%) had target lesion revascularization. Two (1.1%) patients had acute stent thrombosis yielding nonfatal myocardial infarction. In 70 patients (63 ± 14 years, 61 men), quantitative coronary angiography at 6-month follow-up revealed diameter stenosis of 24.1 ± 13.7% and minimal lumen diameter of 2.29 ± 0.56 mm, yielding a late lumen loss of 0.13 ± 0.14 mm.
In real-world setting, implantation of a new-generation polymer-free BES during STEMI is associated with favorable clinical and angiographic results, pointing toward the overall efficacy and safety of the device in complex clinical scenarios.
本研究旨在评估新一代无聚合物生物雷帕霉素洗脱支架(BES)在ST段抬高型心肌梗死(STEMI)真实世界患者中的性能。
早期药物洗脱支架的聚合物成分与延迟动脉愈合、血管重塑和延迟支架血栓形成的发病机制有关。最近,一种新型无聚合物BES在临床试验中显示出优异的临床性能。
本研究共纳入175例因STEMI接受BioFreedom(瑞士莫尔日的Biosensors Europe公司)无聚合物BES治疗的连续患者(64±14岁,141例男性)。主要终点是主要不良心脏事件(MACE)发生率,MACE是1年随访时心脏死亡、再发心肌梗死和缺血驱动的靶血管血运重建的复合终点。一组亚组患者接受了6个月的血管造影随访。STEMI后双联抗血小板治疗持续12个月。
1年时,MACE累积发生率为4.6%。1例患者(0.6%)发生心律失常性心脏死亡,5例患者(2.9%)发生缺血驱动的靶血管血运重建,尽管只有3例患者(1.7%)发生靶病变血运重建。2例患者(1.1%)发生急性支架血栓形成,导致非致命性心肌梗死。在70例患者(63±14岁,61例男性)中,6个月随访时的定量冠状动脉造影显示直径狭窄为24.1±13.7%,最小管腔直径为2.29±0.56 mm,晚期管腔丢失为0.13±0.14 mm。
在真实世界中,STEMI期间植入新一代无聚合物BES与良好的临床和血管造影结果相关,表明该装置在复杂临床情况下的总体有效性和安全性。