Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
J Am Coll Cardiol. 2011 Mar 15;57(11):1264-70. doi: 10.1016/j.jacc.2010.10.035.
The purpose of this study was to determine whether cilostazol reduces intimal hyperplasia in patients undergoing long zotarolimus-eluting stent implantation (stent length: ≥ 30 mm) for native long coronary lesions (length: ≥ 25 mm).
Restenosis after drug-eluting stent implantation remains a significant clinical problem in long coronary lesions.
Patients (n = 499) were assigned randomly to triple (aspirin, clopidogrel, and cilostazol, triple group: n = 250) or dual antiplatelet therapy (aspirin and clopidogrel and placebo, dual group: n = 249) for 8 months after long zotarolimus-eluting stent implantation. The primary end point was in-stent late loss at the 8-month angiography according to the intention-to-treat principle.
The 2 groups had similar baseline characteristics. The in-stent (0.56 ± 0.55 mm vs. 0.68 ± 0.59 mm, p = 0.045) and in-segment (0.32 ± 0.54 mm vs. 0.47 ± 0.54 mm, p = 0.006) late loss were significantly lower in the triple versus dual group, as were 8-month in-stent restenosis (10.8% vs. 19.1%, p = 0.016), in-segment restenosis (12.2% vs. 20.0%, p = 0.028), and 12-month ischemic-driven target lesion revascularization (5.2% vs. 10.0%, p = 0.042) rates. At 12 months, major adverse cardiac events including death, myocardial infarction, and ischemic-driven target lesion revascularization tended to be lower in the triple group than the dual group (7.2% vs. 12.0%, p = 0.07). Percent intimal hyperplasia volume by volumetric intravascular ultrasound analysis was reduced from 27.1 ± 13.2% for the dual group to 22.1 ± 9.9% for the triple group (p = 0.017).
Patients receiving triple antiplatelet therapy after long zotarolimus-eluting stent implantation had decreased extent of late luminal loss, percent intimal hyperplasia volume, and angiographic restenosis, resulting in a reduced risk of 12-month target lesion revascularization compared with patients receiving dual antiplatelet therapy. (Triple Versus Dual Antiplatelet Therapy after ABT578-Eluting Stent; NCT00589927).
本研究旨在确定西洛他唑是否可减少接受长佐他莫司洗脱支架植入(支架长度≥30mm)治疗的原发性长冠状动脉病变(长度≥25mm)患者的内膜增生。
药物洗脱支架植入后再狭窄仍然是长冠状动脉病变的一个重要临床问题。
将 499 名患者随机分为三联(阿司匹林、氯吡格雷和西洛他唑,三联组:n=250)或双联(阿司匹林和氯吡格雷及安慰剂,双联组:n=249)抗血小板治疗 8 个月,对长佐他莫司洗脱支架植入后的患者进行治疗。主要终点为根据意向治疗原则在 8 个月时的血管造影内支架晚期丢失。
两组基线特征相似。与双联组相比,三联组的支架内(0.56±0.55mm 比 0.68±0.59mm,p=0.045)和支架内节段(0.32±0.54mm 比 0.47±0.54mm,p=0.006)晚期丢失以及 8 个月时的支架内再狭窄(10.8%比 19.1%,p=0.016)、支架内节段再狭窄(12.2%比 20.0%,p=0.028)和 12 个月时的缺血驱动的靶病变血运重建(5.2%比 10.0%,p=0.042)发生率均较低。12 个月时,三联组主要不良心脏事件(包括死亡、心肌梗死和缺血驱动的靶病变血运重建)发生率低于双联组(7.2%比 12.0%,p=0.07)。通过血管内超声分析的定量内膜增生体积显示,双联组的内膜增生体积百分比从 27.1±13.2%减少到三联组的 22.1±9.9%(p=0.017)。
与接受双联抗血小板治疗的患者相比,接受长佐他莫司洗脱支架植入后三联抗血小板治疗的患者,晚期管腔丢失、内膜增生体积百分比和血管造影再狭窄程度均有所减轻,12 个月时靶病变血运重建的风险降低。(ABT578 洗脱支架后三联与双联抗血小板治疗;NCT00589927)