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首页> 外文期刊>Catheterization and cardiovascular interventions: Official journal of the Society for Cardiac Angiography & Interventions >Comparison between ticlopidine and clopidogrel in patients undergoing primary stenting in acute myocardial infarction: results from the CADILLAC trial.
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Comparison between ticlopidine and clopidogrel in patients undergoing primary stenting in acute myocardial infarction: results from the CADILLAC trial.

机译:急性心肌梗死初次置入支架的患者中噻氯匹定和氯吡格雷的比较:CADILLAC试验的结果。

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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.
机译:目的:本文的目的是检查氯吡格雷和噻氯匹定对接受急性心肌梗死(AMI)支架置入术的患者是否产生相似的临床结果。背景:先前的研究在支架植入后氯吡格雷和噻氯匹定的相对安全性和有效性方面产生了矛盾的结果,有必要对AMI的一次支架置入进行评估。方法:在一项多中心,前瞻性CADILLAC试验中,接受原发性梗塞支架置入术的患者根据操作者的判断,使用噻氯匹定(931例)或氯吡格雷(163例)治疗,然后随访1年。除了基线TIMI 0/1流量外(72.5%氯吡格雷与63.9%噻氯匹定,P = 0.04)相比,基线临床和血管造影特征具有可比性。结果:接受氯吡格雷的患者在医院内的复发性缺血较多(6.1 vs. 2.8%,P = 0.02),在30天时(10.5 vs. 5.8%,P = 0.02),在30天时的中度和重度出血更为严重(7.4 vs. 7.8)。 2.7%,P = 0.002),直到1年的支架血栓形成率相似(P = 0.11)。通过多变量分析,氯吡格雷的使用是医院和30天(P = 0.012)复发缺血的独立预测因素(P = 0.0002);以及在医院以及30天时(P = 0.001)中度和重度出血。结论:尽管噻吩并吡啶类药物具有相似性,但在急性AMI初次置入支架的前30天内,其疗效可能有所不同。需要一项前瞻性随机试验来确认这些发现。

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