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一项关于接受经皮冠状动脉介入治疗(PCI)的急性冠状动脉综合征(ACS)患者血小板功能引导下抗血小板治疗降阶梯的随机试验。急性冠状动脉综合征慢性抗血小板治疗中血小板抑制反应性测试(TROPICAL-ACS)试验的原理与设计。

A randomised trial on platelet function-guided de-escalation of antiplatelet treatment in ACS patients undergoing PCI. Rationale and design of the Testing Responsiveness to Platelet Inhibition on Chronic Antiplatelet Treatment for Acute Coronary Syndromes (TROPICAL-ACS) Trial.

作者信息

Sibbing Dirk, Aradi Dániel, Jacobshagen Claudius, Gross Lisa, Trenk Dietmar, Geisler Tobias, Orban Martin, Gori Tommaso, Hadamitzky Martin, Merkely Béla, Kiss Róbert Gábor, Komócsi András, Dézsi Csaba A, Thalmeier Andreas, Löw Anja, Holdt Lesca, Teupser Daniel, Ince Hüseyin, Felix Stephan B, Parma Radoslaw, Malek Lukasz, Horstkotte Jan, Baylacher Monika, Schwinger Robert, Rieber Johannes, Mudra Harald, Hausleiter Jörg, Huber Kurt, Neumann Franz-Josef, Koltowski Lukasz, Huczek Zenon, Mehilli Julinda, Massberg Steffen

机构信息

Prof. Dr. med. Dirk Sibbing, Medizinische Klinik und Poliklinik I, Ludwig-Maximilians-Universität München, Marchioninistr. 15, 81377 Munich, Germany, E-mail:

出版信息

Thromb Haemost. 2017 Jan 5;117(1):188-195. doi: 10.1160/TH16-07-0557. Epub 2016 Sep 22.

Abstract

Outcomes of acute coronary syndrome (ACS) patients undergoing percutaneous coronary intervention (PCI) have been significantly improved with the use of potent P2Y receptor inhibitors like prasugrel. While most of the ischaemic risk reduction for prasugrel versus clopidogrel was demonstrated in the early treatment period, the risk of bleeding became particularly prominent during the chronic course of therapy. It may therefore be a valid approach to substitute prasugrel for clopidogrel in the early phase of chronic antiplatelet treatment after PCI. In the Testing Responsiveness To Platelet Inhibition On Chronic Antiplatelet Treatment For Acute Coronary Syndromes (TROPICAL-ACS) trial, we aim to compare standard prasugrel therapy with a de-escalating antiplatelet treatment approach guided by platelet function testing (PFT). The study is an investigator-initiated European multicentre, randomised clinical trial in biomarker-positive ACS patients after successful PCI. Two thousand six hundred patients will be randomised prior to hospital discharge in a 1:1 fashion to either receive standard prasugrel therapy (control group) or de-escalating therapy (one-week prasugrel followed by one-week clopidogrel and PFT-guided maintenance therapy from day 14 after hospital discharge, monitoring group). Patients of the monitoring group with high on-clopidogrel platelet reactivity (HPR) based on Multiplate analyzer testing (HPR: ≥ 46U per consensus definition) will be switched back to prasugrel, whereas those without HPR (<46 U) will continue clopidogrel treatment. The overall study treatment duration will be one year in both groups. The primary endpoint of the study is net clinical benefit (combined incidence of cardiovascular death, myocardial infarction, stroke and bleeding ≥ grade 2 according to BARC criteria) one-year after randomisation. TROPICAL-ACS is the first large-scale, randomised controlled trial assessing the clinical value of a PFT-guided de-escalation of antiplatelet treatment in biomarker positive ACS patients undergoing PCI.

摘要

使用强效P2Y受体抑制剂(如普拉格雷)后,接受经皮冠状动脉介入治疗(PCI)的急性冠状动脉综合征(ACS)患者的预后得到了显著改善。虽然普拉格雷与氯吡格雷相比,在早期治疗阶段降低缺血风险的作用最为明显,但在慢性治疗过程中,出血风险变得尤为突出。因此,在PCI术后慢性抗血小板治疗的早期阶段,用普拉格雷替代氯吡格雷可能是一种有效的方法。在急性冠状动脉综合征慢性抗血小板治疗血小板抑制反应测试(TROPICAL - ACS)试验中,我们旨在比较标准普拉格雷治疗与基于血小板功能测试(PFT)的降阶梯抗血小板治疗方法。该研究是一项由研究者发起的欧洲多中心随机临床试验,针对PCI成功后生物标志物阳性的ACS患者。2600名患者将在出院前以1:1的比例随机分组,分别接受标准普拉格雷治疗(对照组)或降阶梯治疗(一周普拉格雷,随后一周氯吡格雷,并从出院后第14天开始进行PFT指导的维持治疗,监测组)。根据多电极血小板功能分析仪测试,监测组中氯吡格雷治疗时血小板高反应性(HPR:根据共识定义≥46U)的患者将换回普拉格雷,而无HPR(<46U)的患者将继续氯吡格雷治疗。两组的总体研究治疗时长均为一年。该研究的主要终点是随机分组一年后的净临床获益(心血管死亡、心肌梗死、中风以及根据BARC标准出血≥2级的综合发生率)。TROPICAL - ACS是首个评估PFT指导的抗血小板治疗降阶梯在接受PCI的生物标志物阳性ACS患者中的临床价值的大规模随机对照试验。

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