Division of Cardiology, Eulji University Hospital, Daejeon, Korea.
Circ J. 2012;76(5):1102-8. doi: 10.1253/circj.cj-11-1313. Epub 2012 Mar 1.
Positive peri-stent vascular remodeling (PPVR) after drug-eluting stent (DES) implantation is an important mechanism of late-acquired stent malapposition (LASM).
A total of 226 patients (sirolimus-eluting stent [SES], n=105; paclitaxel-eluting stent [PES], n=121) from the Poststent Optimal Stent Expansion Trial who underwent a post-intervention and 9-month follow-up intravascular ultrasound were followed clinically for 5 years. PPVR was arbitrarily defined as a >10% increase in the external elastic membrane volume index at follow-up. PPVR and LASM occurred more frequently with SESs than with PESs. The 5-year rate of major adverse cardiac events was lower with SES than with PES (10.7% vs. 23.2%, P=0.002). The late and very late stent thrombosis (ST) rate was similar between the 2 DES types, but it was higher in patients with PPVR than in those without PPVR (8.8% vs. 1.3%, P=0.009) regardless of the DES type. Early discontinuation (<1 year) of dual antiplatelet therapy (DAPT; hazard ratio [HR], 24.14; 95% confidence interval [CI]: 4.90-118.87; P<0.001), PPVR (HR, 14.94; 95%CI: 1.85-120.46; P=0.011), LASM (HR, 8.01; 95%CI: 1.93-33.16; P=0.004), and stent length (HR, 1.14; 95%CI: 0.98-1.32 per mm; P=0.078) were associated with increased risk of late and very late ST.
PPVR and LASM development after DES implantation, along with early discontinuation of DAPT and longer stent length, are important risk factors of late and very late ST.
药物洗脱支架(DES)植入后正向血管重构(PPVR)是晚期获得支架贴壁不良(LASM)的重要机制。
共纳入 226 例(西罗莫司洗脱支架[SES],n=105;紫杉醇洗脱支架[PES],n=121)来自 Poststent Optimal Stent Expansion Trial 的患者,这些患者在介入治疗后和 9 个月时进行了血管内超声随访,并在临床上进行了 5 年随访。PPVR 被任意定义为随访时外膜弹性膜体积指数增加>10%。SES 比 PES 更容易发生 PPVR 和 LASM。SES 组的 5 年主要不良心脏事件发生率低于 PES 组(10.7%比 23.2%,P=0.002)。两种 DES 类型的晚期和极晚期支架血栓形成(ST)发生率相似,但在有 PPVR 的患者中高于无 PPVR 的患者(8.8%比 1.3%,P=0.009),无论 DES 类型如何。双重抗血小板治疗(DAPT)早期停药(<1 年)(危险比[HR],24.14;95%置信区间[CI]:4.90-118.87;P<0.001)、PPVR(HR,14.94;95%CI:1.85-120.46;P=0.011)、LASM(HR,8.01;95%CI:1.93-33.16;P=0.004)和支架长度(HR,每毫米 1.14;95%CI:0.98-1.32;P=0.078)与晚期和极晚期 ST 的风险增加相关。
DES 植入后 PPVR 和 LASM 的发展以及 DAPT 的早期停药和更长的支架长度是晚期和极晚期 ST 的重要危险因素。