Heart Institute, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
JACC Cardiovasc Interv. 2009 Dec;2(12):1227-35. doi: 10.1016/j.jcin.2009.10.001.
The E-Five registry was designed to evaluate the safety and effectiveness of the Endeavor zotarolimus-eluting stent (ZES) (Medtronic CardioVascular, Santa Rosa, California) for the treatment of coronary artery stenosis across a wide range of patients treated in real-world clinical practice settings.
Early clinical trials with the Endeavor ZES have demonstrated low rates of target lesion revascularization with a favorable safety profile including low late stent thrombosis with up to 4 years of follow-up. A clinical registry was designed to complement controlled trial data by examining a large patient population, including high-risk patient subsets.
The E-Five registry is a prospective, nonrandomized, multicenter global registry conducted at 188 centers worldwide. Adult patients (n = 8,314) with coronary artery disease who underwent single-vessel or multivessel percutaneous coronary intervention were enrolled. The primary end point was the rate of major adverse cardiac events (MACE) at 12 months. A secondary analysis stratified patients by standard versus extended-use clinical and lesion characteristics.
Overall 12-month outcome rates were MACE 7.5%; cardiac death 1.7%; myocardial infarction (all) 1.6%; target lesion revascularization 4.5%; and stent thrombosis (Academic Research Consortium definite and probable) 1.1%. The 12-month MACE rates were 4.3% and 8.6% for standard- and extended-use patients, respectively (p < 0.001).
This large, international multicenter registry provides important information regarding the long-term safety and efficacy of the Endeavor ZES across standard and extended-use patients in the real-world setting. Rates of MACE and measures of safety including cardiac death, myocardial infarction, and stent thrombosis were low and consistent with pooled results of clinical trials. (E-Five Registry: A World-Wide Registry With The Endeavor Zotarolimus Eluting Coronary Stent [eFive Registry]; NCT00623441).
E-Five 注册研究旨在评估 Endeavor 佐他莫司洗脱支架(ZES)(美敦力心血管,加利福尼亚州圣罗莎)在真实世界临床实践环境中治疗广泛患者的冠状动脉狭窄的安全性和有效性。
早期临床试验显示, Endeavor ZES 的靶病变血运重建率较低,安全性良好,包括在长达 4 年的随访中晚期支架血栓形成率较低。设计临床注册研究是为了通过检查大量患者人群(包括高危患者亚组),补充对照试验数据。
E-Five 注册研究是一项前瞻性、非随机、多中心全球注册研究,在全球 188 个中心进行。纳入接受单支或多支经皮冠状动脉介入治疗的成年冠心病患者(n=8314)。主要终点为 12 个月时主要不良心脏事件(MACE)的发生率。二次分析根据标准和延长使用的临床和病变特征对患者进行分层。
总体 12 个月的预后率为 MACE 7.5%;心脏死亡 1.7%;心肌梗死(所有)1.6%;靶病变血运重建 4.5%;支架血栓形成(学术研究联合会确定和可能)1.1%。标准使用和延长使用患者的 12 个月 MACE 发生率分别为 4.3%和 8.6%(p<0.001)。
这项大型国际多中心注册研究提供了关于 Endeavor ZES 在真实世界环境中标准和延长使用患者的长期安全性和疗效的重要信息。MACE 发生率和安全性指标(包括心脏死亡、心肌梗死和支架血栓形成)较低,与临床试验的汇总结果一致。(E-Five 注册研究: Endeavor 佐他莫司洗脱冠状动脉支架的全球注册研究 [eFive 注册研究];NCT00623441)。