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基于聚合物的紫杉醇洗脱支架治疗复杂长冠状动脉病变的多中心随机试验临床疗效:支持药物洗脱支架在当代临床实践中的应用

Clinical efficacy of polymer-based paclitaxel-eluting stents in the treatment of complex, long coronary artery lesions from a multicenter, randomized trial: support for the use of drug-eluting stents in contemporary clinical practice.

作者信息

Dawkins Keith D, Grube Eberhard, Guagliumi Giulio, Banning Adrian P, Zmudka Krzysztof, Colombo Antonio, Thuesen Leif, Hauptman Karl, Marco Jean, Wijns William, Popma Jeffrey J, Koglin Joerg, Russell Mary E

机构信息

Southampton University Hospital, Southampton, UK.

出版信息

Circulation. 2005 Nov 22;112(21):3306-13. doi: 10.1161/CIRCULATIONAHA.105.552190. Epub 2005 Nov 14.

Abstract

BACKGROUND

Intracoronary polymer-based stent delivery of paclitaxel has been shown to be effective in reducing restenosis in simple coronary lesions, but the evidence base for contemporary use in longer, more complex coronary stenoses is lacking.

METHODS AND RESULTS

TAXUS VI is a prospective, multicenter, double-blind, randomized trial assessing clinical and angiographic outcomes of the TAXUS Moderate Release paclitaxel-eluting stent in the treatment of long, complex coronary artery lesions. Four hundred forty-eight patients at 44 sites were randomized (1:1) between a drug-eluting TAXUS Express2 and an uncoated Express2 control stent. Per protocol, the 9-month follow-up included an angiographic reevaluation in all patients. The primary end point was the rate of target-vessel revascularization 9 months after the study procedure; secondary end points included the rate of target-lesion revascularization and binary restenosis at follow-up. Mean lesion length in the study was 20.6 mm, with a mean stent-covered length of 33.4 mm. Of all lesions, 55.6% were classified as complex lesions (type C of the AHA/ACC classification). At 9 months, target-vessel revascularization was 9.1% in the TAXUS group and 19.4% in the control group (P=0.0027; relative reduction, 53%). Target-lesion revascularization was reduced from 18.9% to 6.8%, respectively (P=0.0001). The incidence of major adverse cardiac events was similar in the 2 groups, 16.4% and 22.5% in TAXUS and control, respectively (P=0.12), including comparable rates for acute myocardial infarction. Binary restenosis in the stented area was reduced from 32.9% in the control group to 9.1% in the TAXUS patients (P<0.0001).

CONCLUSIONS

The finding that the TAXUS Moderate Release stent system is safe and effective in the treatment of long, complex coronary artery lesions provides the evidence base for the more widespread use of drug-eluting stents in contemporary clinical practice.

摘要

背景

冠状动脉内基于聚合物的紫杉醇支架植入已被证明可有效减少简单冠状动脉病变的再狭窄,但目前缺乏在更长、更复杂的冠状动脉狭窄中应用的证据基础。

方法与结果

TAXUS VI是一项前瞻性、多中心、双盲、随机试验,评估TAXUS中度释放紫杉醇洗脱支架治疗长段复杂冠状动脉病变的临床和血管造影结果。44个中心的448例患者被随机(1:1)分为药物洗脱TAXUS Express2支架组和无涂层Express2对照支架组。按照方案,9个月的随访包括对所有患者进行血管造影复查。主要终点是研究操作后9个月的靶血管血运重建率;次要终点包括随访时的靶病变血运重建率和二元再狭窄率。研究中病变平均长度为20.6 mm,支架覆盖平均长度为33.4 mm。所有病变中,55.6%被分类为复杂病变(AHA/ACC分类的C型)。9个月时,TAXUS组的靶血管血运重建率为9.1%,对照组为19.4%(P = 0.0027;相对降低53%)。靶病变血运重建率分别从18.9%降至6.8%(P = 0.0001)。两组主要不良心脏事件发生率相似,TAXUS组和对照组分别为16.4%和22.5%(P = 0.12),包括急性心肌梗死发生率相当。支架置入区域的二元再狭窄率从对照组的32.9%降至TAXUS组患者的9.1%(P < 0.0001)。

结论

TAXUS中度释放支架系统在治疗长段复杂冠状动脉病变中安全有效的这一发现,为当代临床实践中更广泛使用药物洗脱支架提供了证据基础。

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