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首页> 外文期刊>International Journal of Cardiology >Long-term clinical outcome with titanium-nitride-oxide-coated stents and paclitaxel-eluting stents for coronary revascularization in an unselected population.
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Long-term clinical outcome with titanium-nitride-oxide-coated stents and paclitaxel-eluting stents for coronary revascularization in an unselected population.

机译:氮氧化钛涂层支架和紫杉醇洗脱支架在未选定人群中的冠状动脉血运重建的长期临床结果。

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摘要

BACKGROUND: The aim of this study was to evaluate long-term clinical events in patients treated with titanium-nitride-oxide-coated bio-active stents (BAS) and paclitaxel-eluting stents (PES) in routine clinical practice. METHODS: All patients undergoing percutaneous coronary intervention (PCI) were eligible for this single-centre registry between May 2003 and November 2004. The primary end point of the study was major adverse cardiac events (MACE) at 3 years including myocardial infarction (MI), cardiac death and target vessel revascularization (TVR). RESULTS: A total of 201 patients received BAS and 204 patients PES. In addition, during the same study period, 184 patients were treated with bare-metal stents (BMS) and 125 patients underwent CABG. Complete follow-up datasets were available in all patients. After 3 years of follow-up, the rate of MACE was 13.9% for BAS and 23.5% for PES (adjusted HR 2.0, 95% CI 1.2-3.2, p=0.006). This difference was mainly driven by a higher incidence of MI in the PES group (19.1%) compared with the BAS (7.5%) group (adjusted HR 3.2, 95% CI 1.7-5.8, p<0.001). The rate of MACE was 31.5% in the BMS group and 4% in the CABG group. At 3 years, stent thrombosis occurred in 15 patients in the PES (7.4%) group. There was no stent thrombosis in the BAS group. CONCLUSIONS: After the 3 year follow-up, BAS resulted in better long-term outcome compared with PES with infrequent need for TVR.
机译:背景:这项研究的目的是评估常规临床实践中使用氮化钛氧化物生物活性支架(BAS)和紫杉醇洗脱支架(PES)治疗的患者的长期临床事件。方法:2003年5月至2004年11月之间,所有接受经皮冠状动脉介入治疗(PCI)的患者均符合该单中心登记的条件。研究的主要终点是3年时的主要不良心脏事件(MACE),包括心肌梗塞(MI) ,心脏死亡和目标血管血运重建(TVR)。结果:总共201例患者接受了BAS,204例患者接受了PES。此外,在同一研究期间,有184例患者接受了裸金属支架(BMS)治疗,有125例患者接受了CABG。在所有患者中都有完整的随访数据集。经过3年的随访,BAS的MACE率为13.9%,PES的MACE率为23.5%(调整后的HR 2.0、95%CI 1.2-3.2,p = 0.006)。这种差异主要是由PES组(19.1%)相比BAS组(7.5%)组的MI发生率更高(校正后的HR 3.2、95%CI 1.7-5.8,p <0.001)引起的。 BMS组的MACE率为31.5%,CABG组的MACE率为4%。在3年时,PES组(7.4%)中有15例发生了支架血栓形成。 BAS组无支架血栓形成。结论:3年的随访后,与不需要TVR的PES相比,BAS可带来更好的长期疗效。

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