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急性心肌梗死直接支架置入患者中噻氯匹定与氯吡格雷的比较:CADILLAC试验结果

Comparison between ticlopidine and clopidogrel in patients undergoing primary stenting in acute myocardial infarction: results from the CADILLAC trial.

作者信息

Lansky Alexandra J, Tsuchiya Yoshihiro, Brener Micheal, Mehran Roxana, Cristea Ecaterina, Pietras Cody, Grines Cindy L, Cox David A, Garcia Eulogio, Tcheng James E, Guagliumi Giulio, Stuckey Thomas, Turco Mark, Carroll John D, Rutherford Barry D, Leon Martin B, Moses Jeffrey, Stone Gregg W

机构信息

Columbia University Medical Center, Department of Cardiology, Cardiovascular Research Foundation, New York, New York 10022, USA.

出版信息

Catheter Cardiovasc Interv. 2008 Dec 1;72(7):917-24. doi: 10.1002/ccd.21714.

Abstract

OBJECTIVE

The aim of this article is to examine whether clopidogrel and ticlopidine treatments produce similar clinical outcomes for patients receiving primary stenting for acute myocardial infarction (AMI).

BACKGROUND

Prior studies have yielded conflicting results on the relative safety and efficacy of clopidogrel and ticlopidine after stent implantation, warranting an evaluation in primary stenting for AMI.

METHODS

In the multicenter, prospective CADILLAC trial, patients undergoing primary infarct stenting were treated at operator discretion with either ticlopidine (931 patients) or clopidogrel (163 patients) and then followed for 1 year. Baseline clinical and angiographic characteristics were comparable except for baseline TIMI 0/1 flow (72.5% clopidogrel vs. 63.9% ticlopidine, P = 0.04).

RESULTS

Patients receiving clopidogrel had more recurrent ischemia in hospital (6.1 vs. 2.8%, P = 0.02) and at 30 days (10.5 vs. 5.8%, P = 0.02), more moderate and severe bleeding at 30 days (7.4 vs. 2.7%, P = 0.002), and similar rates of stent thrombosis out to 1 year (P = 0.11). By multivariable analysis, clopidogrel use was an independent predictor for recurrent ischemia in hospital (P = 0.0002), and at 30 days (P = 0.012); and of moderate and severe bleeding in hospital (P = 0.002), and at 30 days (P = 0.001).

CONCLUSIONS

Despite thienopyridines similarities, their efficacy may be different within the first 30 days of primary stenting for AMI. A prospective, randomized trial is required to confirm these findings.

摘要

目的

本文旨在研究对于接受急性心肌梗死(AMI)直接支架置入术的患者,氯吡格雷和噻氯匹定治疗是否会产生相似的临床结果。

背景

先前的研究对于支架植入术后氯吡格雷和噻氯匹定的相对安全性和有效性得出了相互矛盾的结果,因此有必要对AMI直接支架置入术进行评估。

方法

在多中心、前瞻性CADILLAC试验中,接受梗死相关动脉直接支架置入术的患者由术者决定给予噻氯匹定(931例患者)或氯吡格雷(163例患者)治疗,随后随访1年。除基线TIMI 0/1血流情况外(氯吡格雷组为72.5%,噻氯匹定组为63.9%,P = 0.04),两组患者的基线临床和血管造影特征具有可比性。

结果

接受氯吡格雷治疗的患者在住院期间(6.1%对2.8%,P = 0.02)和30天时(10.5%对5.8%,P = 0.02)有更多的再发缺血事件,30天时出现更多中重度出血(7.4%对2.7%,P = 0.002),至1年时支架血栓形成率相似(P = 0.11)。通过多变量分析,使用氯吡格雷是住院期间(P = 0.0002)和30天时(P = 0.012)再发缺血事件的独立预测因素;也是住院期间(P = 0.002)和30天时(P = 0.001)中重度出血的独立预测因素。

结论

尽管噻吩并吡啶类药物有相似之处,但在AMI直接支架置入术的最初30天内,它们的疗效可能不同。需要进行一项前瞻性随机试验来证实这些发现。

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