首页> 外文期刊>Cardiology and therapy. >Dual Antithrombotic Therapy with Clopidogrel and Novel Oral Anticoagulants in Patients with Atrial Fibrillation Undergoing Percutaneous Coronary Intervention: A Real-world Study
【24h】

Dual Antithrombotic Therapy with Clopidogrel and Novel Oral Anticoagulants in Patients with Atrial Fibrillation Undergoing Percutaneous Coronary Intervention: A Real-world Study

机译:氯吡格雷和新型口服抗凝剂的双重抗血栓治疗在经皮冠状动脉介入治疗的房颤患者中的应用:一项真实世界的研究

获取原文
       

摘要

IntroductionFor patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI), proper antithrombotic therapy is equivocal. Current guidelines recommend triple therapy, which carries a high risk of bleeding. Recent large trials suggest that dual therapy (DT) with novel oral anticoagulant (NOAC) plus P2Y12 inhibitor can be an appropriate alternative, but real-world data for this alternative are scarce and the optimal duration of DT has not yet been established. MethodsThis analysis was performed in a single-center prospective cohort. We investigated 216 PCI patients with indication for anticoagulation due to AF. After PCI patients received DT with reduced doses NOAC plus P2Y12 inhibitor for 6?months, which was followed by standard dose NOAC monotherapy. Efficacy endpoints were defined as cardiac death, myocardial infarction (MI), stent thrombosis (ST), and stroke. Safety endpoints were bleeding events as defined by Bleeding Academic Consortium (BARC). ResultsBaseline characteristics of our study population were described by a CHA2DS2-VASc score of greater than 4 and a HAS-BLED score of greater than 3. After a mean follow-up of 18.7?months, efficacy events occurred in 12 patients (5.6%). We observed three (1.4%) cardiac deaths, two (0.9%) MIs, six (2.8%) strokes, and one (0.5%) definite ST. After switching from DT to NOAC monotherapy after 6.3?±?1.7?months, there was no rebound of ischemic events. Bleeding events occurred in 34 patients (15.7%) mainly under DT, while bleeding was less during NOAC monotherapy. ConclusionsIn this long-term study of high-risk and real-world AF-patients with PCI, DT with NOAC and P2Y12 inhibitor (6?months) followed by NOAC monotherapy was safe and effective.
机译:简介对于正在接受经皮冠状动脉介入治疗(PCI)的房颤(AF)患者,适当的抗血栓治疗是模棱两可的。当前的指南建议采用三联疗法,这种疗法具有很高的出血风险。最近的大型试验表明,采用新型口服抗凝剂(NOAC)加P2Y 12 抑制剂的双重疗法(DT)可能是一种合适的替代方法,但这种替代方法的实际数据很少,并且DT的最佳持续时间尚未建立。方法本研究在单中心前瞻性队列中进行。我们调查了216位有AF指征的抗凝指征的PCI患者。 PCI患者接受减量剂量的NOAC加P2Y 12 抑制剂DT后6个月,然后进行标准剂量的NOAC单药治疗。疗效终点定义为心源性死亡,心肌梗塞(MI),支架血栓形成(ST)和中风。安全终点是出血事件,如出血学术协会(BARC)所定义。结果我们的研究人群的基线特征由CHA 2 DS 2 -VASc得分大于4和HAS-BLED得分大于3来描述。在长达18.7个月的时间里,有12例患者发生了疗效事件(5.6%)。我们观察到三例(1.4%)心源性死亡,两例(0.9%)心梗,六例(2.8%)中风和一例(0.5%)明确的ST。在6.3±1.7个月后从DT改为NOAC单药治疗后,没有缺血事件的反弹。主要在DT下进行的出血事件发生在34例患者中(15.7%),而在NOAC单药治疗期间出血较少。结论在这项对PCI高危,现实世界房颤患者的长期研究中,采用NOAC和P2Y 12 抑制剂治疗DT(6个月),然后进行NOAC单一疗法是安全有效的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号