Cho Sang Cheol, Jeong Myung Ho, Kim Wan, Ahn Youngkeun, Hong Young Joon, Kim Young Jo, Kim Chong Jin, Cho Myeong Chan, Han Kyoo Rok, Kim Hyo Soo
Department of Cardiology, Gwangju Veterans Hospital, Gwangju, Republic of Korea.
Department of Cardiology, Chonnam National University Hospital, Gwangju, Republic of Korea.
J Cardiol. 2014 Jun;63(6):409-17. doi: 10.1016/j.jjcc.2013.10.016. Epub 2013 Dec 5.
There were limited data about comparison of zotarolimus-eluting stents (ZES) and everolimus-eluting stents (EES) in patients with small coronary artery disease (CAD), especially in patients with acute myocardial infarction (AMI). The objective of this study was to compare the clinical outcomes of ZES and EES in patients with AMI for small CAD.
A total 1565 AMI patients treated with Endeavor-ZES (n=651) (Medtronic CardioVascular, Santa Rosa, CA, USA) or Xience V/Promus-EES (n=914) (Abbott Vascular, Temecula, CA/Boston Scientific, Natick, MA, USA) for small CAD (stent diameter ≤ 2.75 mm) in KAMIR (Korea Acute Myocardial Infarction Registry) were enrolled. After propensity score matching to adjust for baseline clinical and angiographic characteristics, we compared a total 1302 patients (651 ZES and 651 EES) about major adverse cardiac events (MACE) at 1-year. Subgroup analysis about 1-year clinical outcomes was undertaken in patients who were discharged alive.
Baseline clinical and angiographic characteristics were similar between the two groups after propensity score matching. Total MACE did not differ between the two groups before (9.8% vs. 8.2%, p=0.265) and after (9.8% vs. 9.4%, p=0.778) propensity score matching. The EES group showed lower rate of 1-year cardiac death (5.4% vs. 3.3%, p=0.041), target lesion failure (TLF; 6.9% vs. 4.3%, p=0.022), and stent thrombosis (1.4% vs. 0.4%, p=0.042) compared with the ZES group. However, there were no differences in 1-year cardiac death, TLF, and stent thrombosis in propensity score matched populations. Other various 1-year clinical outcomes showed no difference between the two groups. Subgroup analysis in patients who were discharged alive showed similar outcomes between the two groups at 1-year follow-up.
In-this propensity score matched analysis, EES and ZES showed no significant difference in clinical outcomes at 1-year follow-up in patients with AMI for small CAD.
关于佐他莫司洗脱支架(ZES)与依维莫司洗脱支架(EES)在冠状动脉疾病(CAD)较小的患者中的比较数据有限,尤其是在急性心肌梗死(AMI)患者中。本研究的目的是比较ZES和EES在患有小CAD的AMI患者中的临床结局。
在韩国急性心肌梗死注册研究(KAMIR)中,共有1565例因小CAD(支架直径≤2.75mm)接受安珂佐他莫司洗脱支架(ZES,n = 651)(美敦力心血管公司,美国加利福尼亚州圣罗莎)或雅培依维莫司洗脱支架/波士顿科学公司依维莫司洗脱支架(Xience V/Promus-EES,n = 914)(雅培血管公司,美国加利福尼亚州特梅库拉/波士顿科学公司,美国马萨诸塞州纳蒂克)治疗的AMI患者被纳入研究。在进行倾向评分匹配以调整基线临床和血管造影特征后,我们比较了1302例患者(651例ZES和651例EES)1年时的主要不良心脏事件(MACE)。对存活出院的患者进行了1年临床结局的亚组分析。
倾向评分匹配后,两组的基线临床和血管造影特征相似。在倾向评分匹配前(9.8%对8.2%,p = 0.265)和匹配后(9.8%对9.4%,p = 0.778),两组的总MACE无差异。与ZES组相比,EES组1年心脏死亡率(5.4%对3.3%,p = 0.041)、靶病变失败率(TLF;6.9%对4.3%,p = 0.022)和支架血栓形成率(1.4%对0.4%,p = 0.042)较低。然而,在倾向评分匹配的人群中,1年心脏死亡、TLF和支架血栓形成方面无差异。其他各种1年临床结局在两组之间无差异。对存活出院患者的亚组分析显示,两组在1年随访时结局相似。
在这项倾向评分匹配分析中,对于患有小CAD的AMI患者,EES和ZES在1年随访时的临床结局无显著差异。