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Impact of Dabigatran versus Phenprocoumon on ADP Induced Platelet Aggregation in Patients with Atrial Fibrillation with or without Concomitant Clopidogrel Therapy (the Dabi-ADP-1 and Dabi-ADP-2 Trials)

机译:达比加群vs苯丙酮对房颤合并或不合并氯吡格雷治疗的房颤患者ADP诱导的血小板聚集的影响(Dabi-ADP-1和Dabi-ADP-2试验)

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摘要

Background. A relevant number of patients receive triple therapy with clopidogrel, aspirin, and oral anticoagulation. Clopidogrel's efficacy on ADP induced platelet function may be influenced by concomitant antithrombotic therapies. Data regarding the effect of dabigatran on platelet function is limited to in vitro studies and healthy individuals. Methods. The “Dabi-ADP-1” and “Dabi-ADP-2” trials randomized patients with atrial fibrillation to either dabigatran or phenprocoumon for a 2-week period. In Dabi-ADP-1 (n = 70) patients with clopidogrel therapy were excluded and in Dabi-ADP-2 (n = 46) patients had to be treated concomitantly with clopidogrel. The primary endpoint was ADP-induced platelet aggregation between dabigatran and phenprocoumon at 14 days. Secondary endpoints were ADPtest HS-, TRAP-, and COL-induced platelet aggregation. Results. There was no significant difference regarding the primary endpoint between both groups in either trial (Dabi-ADP-1: Dabigatran: 846 [650–983] AU × min versus phenprocoumon: 839 [666–1039] AU × min, P = 0.90 and Dabi-ADP-2: 326 [268–462] versus 350 [214–535], P = 0.70) or regarding the secondary endpoints, ADPtest HS-, TRAP-, and COL-induced platelet aggregation. Conclusion. Dabigatran as compared to phenprocoumon has no impact on ADP-induced platelet aggregation in atrial fibrillation patients neither with nor without concomitant clopidogrel therapy.
机译:背景。相当多的患者接受了氯吡格雷,阿司匹林和口服抗凝三联疗法。氯吡格雷对ADP诱导的血小板功能的疗效可能会受到抗栓治疗的影响。关于达比加群对血小板功能影响的数据仅限于体外研究和健康个体。方法。 “ Dabi-ADP-1”和“ Dabi-ADP-2”试验将患有房颤的患者随机分为达比加群或苯普卡蒙,为期2周。在Dabi-ADP-1(n = 70)中,使用氯吡格雷治疗的患者被排除在外;在Dabi-ADP-2(n = 46)中,患者必须同时使用氯吡格雷治疗。主要终点是在14天时ADP诱导的达比加群和苯普鲁蒙之间的血小板聚集。次要终点是ADPtest HS-,TRAP-和COL诱导的血小板聚集。结果。在两项试验中,两组之间的主要终点均无显着差异(Dabi-ADP-1:达比加群:846 [650–983] AU×min与苯普鲁蒙:839 [666–1039] AU×min,P = 0.90和Dabi-ADP-2:326 [268-462]与350 [214-535],P = 0.70),或就次要终点而言,ADPtest HS-,TRAP-和COL诱导的血小板聚集。结论。与苯丙香酚相比,达比加群对有或无氯吡格雷治疗的房颤患者的ADP诱导的血小板聚集均无影响。

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