Department of Translational Medical Sciences, University of Campania, Caserta, Italy.
Cardiology Unit, Ospedale "Sant'Anna e San Sebastiano", Caserta, Italy.
Catheter Cardiovasc Interv. 2019 Dec 1;94(7):972-979. doi: 10.1002/ccd.28305. Epub 2019 Apr 29.
The ULISSE registry has demonstrated the real-world performance of the Ultimaster biodegradable polymer sirolimus-eluting stent (BP-SES) in a large cohort of patients undergoing percutaneous coronary intervention, including a large proportion of patients presenting with acute myocardial infarction (AMI).
We performed a subgroup analysis of the ULISSE registry in AMI patients and compared the outcomes of this vulnerable cohort with that of patients presenting without AMI (non-AMI). The primary end point was the incidence of 1-year target lesion failure (TLF), a composite of cardiac death, target vessel myocardial infarction (TV-MI), and clinically indicated target lesion revascularization (TLR).
Of 1,660 patients included in the ULISSE registry, 381(23%) presented with AMI, 207(54.3%) non-ST elevation myocardial infarction, and 174(45.7%) ST-elevation myocardial infarction. Compared with non-AMI patients, those with AMI were more frequently female and smokers, with lower left ventricular ejection fraction (LVEF) and chronic kidney disease requiring dialysis. At 1 year, TLF rate was significantly higher in AMI than non-AMI patients (7.9 vs. 4.1%; HR 1.98, CI 95% 1.22-3.23; p = .005) driven by higher rate of cardiac death (4.0 vs. 1.1%; HR 3.59, CI 95% 1.64-7.88; p = .01) and TV-MI (2.8 vs 0.9%; HR 2.99,CI 95% 1.22-7.37; p = .01), without differences in TLR rate (4.3 vs. 2.9%,HR 0.66, CI95% 0.35-1.25; p = .2). At multivariate Cox regression analysis, eGFR <40 mL/min (HR: 2.868) and LVEF <40% (HR: 2.394) were the only independent predictors of TLF.
In AMI patients, Ultimaster BP-SES implantation was associated with higher rate of TLF and definite stent thrombosis compared with non-AMI patients. The high incidence of adverse events was mainly driven by the unfavorable baseline risk profile.
ULISSE 注册研究已经证明了 Ultimaster 可生物降解聚合物西罗莫司洗脱支架(BP-SES)在接受经皮冠状动脉介入治疗的大量患者中的真实世界疗效,其中包括很大一部分急性心肌梗死(AMI)患者。
我们对 ULISSE 注册研究中的 AMI 患者进行了亚组分析,并比较了这一脆弱人群与无 AMI(非 AMI)患者的结局。主要终点是 1 年靶病变失败(TLF)的发生率,复合终点包括心源性死亡、靶血管心肌梗死(TV-MI)和临床指征靶病变血运重建(TLR)。
在 ULISSE 注册研究的 1660 例患者中,381 例(23%)为 AMI,207 例(54.3%)为非 ST 段抬高型心肌梗死,174 例(45.7%)为 ST 段抬高型心肌梗死。与非 AMI 患者相比,AMI 患者更常为女性和吸烟者,左心室射血分数(LVEF)更低,且需要透析的慢性肾脏病。1 年时,AMI 患者的 TLF 发生率明显高于非 AMI 患者(7.9%比 4.1%;HR 1.98,95%CI 1.22-3.23;p = 0.005),这主要是由于心源性死亡(4.0%比 1.1%;HR 3.59,95%CI 1.64-7.88;p = 0.01)和 TV-MI(2.8%比 0.9%;HR 2.99,95%CI 1.22-7.37;p = 0.01)发生率较高所致,TLR 发生率无差异(4.3%比 2.9%;HR 0.66,95%CI 0.35-1.25;p = 0.2)。多变量 Cox 回归分析显示,eGFR<40 mL/min(HR:2.868)和 LVEF<40%(HR:2.394)是 TLF 的唯一独立预测因素。
在 AMI 患者中,与非 AMI 患者相比,Ultimaster BP-SES 植入后靶病变失败和明确的支架血栓形成发生率更高。不良事件发生率较高主要是由于基线风险状况不佳。