Department of Cardiology, Clinical Military Hospital, Wroclaw, Poland.
Kardiol Pol. 2013;71(1):25-31.
Recent data from "real world" registries and some randomised trials concerning the safety and efficacy of drug-eluting stents (DES) in patients with acute ST-elevation myocardial infarction (STEMI) are equivocal.
We sought to compare DES with bare-metal stents (BMS) in STEMI patients treated with primary percutaneous coronary intervention in terms of safety and efficacy parameters in long-term follow-up.
895 consecutive STEMI patients admitted between 2003 and 2006 were included in this observational study. The clinical and procedural characteristic as well as long-term outcome of 327 patients treated with DES were compared with 568 patients treated with BMS. Combined primary endpoint consisted of: death, myocardial infarction (MI) and target vessel revascularisation (TVR).
Age, sex, risk factors, presence of 3-vessel disease, left ventricular ejection fraction and the use of IIb/IIIa antagonist were comparable in both groups. During a mean follow-up of 570 ± 490 days, the mortality rate was 8.9% in the DES group vs. 15.5% in the BMS group (p = 0.005). In the DES group, lower incidences of both death and MI (9.5% vs. 16%, p = 0.006) as well as the combined endpoint of death, MI and TVR (19.3% vs. 31.3%, p < 0.001) were recorded. Target lesion revascularisation was more frequently performed in the BMS group (13.4% vs. 8.6%, p = 0.03). However, patients who received BMS more frequently had history of MI and coronary interventions, Killip class > 1 on admission, lower level of haemoglobin and HDL-cholesterol and higher level of troponin than those who received DES. After adjustment, the use of BMS was no longer significantly associated with worse clinical outcome with a trend in favour of DES. The only independent factor associated with increased risk of the combined endpoint was the Killip class > 1 (p = 0.003).
In STEMI patients, DES are not inferior in comparison to BMS in terms of safety and efficacy parameters and seem to be associated with a lower rate of target lesion revascularisations. Additionally, Killip classification remains a simple and important classification used to stratify risk in patients with acute MI.
近期“真实世界”登记研究和一些随机试验的数据显示,药物洗脱支架(DES)在急性 ST 段抬高型心肌梗死(STEMI)患者中的安全性和疗效存在争议。
我们旨在比较直接经皮冠状动脉介入治疗(PCI)治疗的 STEMI 患者中,DES 和金属裸支架(BMS)的安全性和疗效参数的长期随访结果。
本观察性研究纳入了 2003 年至 2006 年间连续收治的 895 例 STEMI 患者。比较了 327 例接受 DES 治疗的患者与 568 例接受 BMS 治疗的患者的临床和手术特征以及长期预后。联合主要终点包括:死亡、心肌梗死(MI)和靶血管血运重建(TVR)。
两组患者的年龄、性别、危险因素、三血管病变、左心室射血分数和使用 IIb/IIIa 拮抗剂情况相似。在平均 570±490 天的随访期间,DES 组的死亡率为 8.9%,BMS 组为 15.5%(p=0.005)。DES 组的死亡率和 MI 发生率均较低(9.5%比 16%,p=0.006),以及死亡、MI 和 TVR 的联合终点发生率也较低(19.3%比 31.3%,p<0.001)。BMS 组的靶病变血运重建更为频繁(13.4%比 8.6%,p=0.03)。然而,接受 BMS 治疗的患者更常患有 MI 和冠状动脉介入史、入院时 Killip 分级>1、血红蛋白和 HDL-胆固醇水平较低、肌钙蛋白水平较高。校正后,BMS 的使用与临床结局恶化不再显著相关,DES 组有改善趋势。唯一与联合终点风险增加相关的独立因素是 Killip 分级>1(p=0.003)。
在 STEMI 患者中,DES 在安全性和疗效参数方面并不逊于 BMS,并且似乎与靶病变血运重建率较低相关。此外,Killip 分级仍然是一种简单而重要的分类方法,用于对急性 MI 患者进行风险分层。