Division of Cardiology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02120, USA.
Catheter Cardiovasc Interv. 2011 Jan 1;77(1):22-8. doi: 10.1002/ccd.22613.
To evaluate the efficacy and safety of drug eluting stents (DES) when compared with bare metal stents (BMS) in patients with moderate to severe calcified coronary lesions.
Calcified coronary lesions present unique technical challenges during percutaneous coronary intervention (PCI) and it is not known if DES are as safe and as effective in the presence of calcium, as randomized trials typically exclude this common patient subset.
We evaluated patients with PCI of a single calcified lesion enrolled across five recruitment waves in the National Heart, Lung, and Blood Institute Dynamic Registry between 1997 and 2006. Patients were divided into two groups based on the stent type- BMS and DES. The primary efficacy outcome was the need for repeat revascularization at 1 year and the primary safety outcome was a composite of death and myocardial infarction at 1 year.
Among the 1,537 patients included in the analysis, 884 (57%) underwent PCI with BMS and 653 (43%) with DES. DES use was associated with a significant reduction in the risk of repeat revascularization (10.0% vs. 15.3%; P = 0.003) with no significant higher risk of primary safety outcome (9.3% vs. 10.5%; P = 0.45) when compared to the BMS group. In a propensity score adjusted analysis, DES use was associated with a significantly lower risk in repeat revascularization (HR = 0.57; 95% CI 0.40-0.82; P = 0.002) and no significant difference in the risk of death and myocardial infarction (HR = 0.78; 95% CI 0.53-1.15; P = 0.20) compared to BMS group.
In this large multicenter registry of patients with a moderate to severe calcified coronary lesion, use of DES compared to BMS was associated with significant reduction in the risk of repeat revascularization without any increase in death and myocardial infarction.
评估药物洗脱支架(DES)与金属裸支架(BMS)在中重度钙化冠状动脉病变患者中的疗效和安全性。
在经皮冠状动脉介入治疗(PCI)中,钙化冠状动脉病变带来了独特的技术挑战,目前尚不清楚 DES 在存在钙的情况下是否与随机试验一样安全有效,因为这些试验通常排除了这种常见的患者亚组。
我们评估了 1997 年至 2006 年期间在国立心肺血液研究所动态注册中心的五个招募波中接受单一钙化病变 PCI 的患者。根据支架类型,将患者分为 BMS 和 DES 两组。主要疗效终点为 1 年内需要再次血运重建,主要安全性终点为 1 年内死亡和心肌梗死的复合终点。
在纳入分析的 1537 例患者中,884 例(57%)接受 BMS 治疗,653 例(43%)接受 DES 治疗。与 BMS 组相比,DES 治疗与再次血运重建风险显著降低相关(10.0% vs. 15.3%;P=0.003),而主要安全性终点无显著更高风险(9.3% vs. 10.5%;P=0.45)。在倾向评分调整分析中,与 BMS 组相比,DES 治疗与再次血运重建风险显著降低相关(HR=0.57;95%CI 0.40-0.82;P=0.002),而死亡和心肌梗死风险无显著差异(HR=0.78;95%CI 0.53-1.15;P=0.20)。
在这项针对中重度钙化冠状动脉病变患者的大型多中心注册研究中,与 BMS 相比,DES 的使用与再次血运重建风险显著降低相关,而死亡和心肌梗死风险无增加。