Cuisset Thomas, Frere Corinne, Quilici Jacques, Uhry Sabrina, Morange Pierre-Emmanuel, Mouret Jean-Philippe, Gaborit Benedicte, Bali Laurent, Moro Pierre-Julien, Lambert Marc, Bonnet Jean Louis
Department of Cardiology, CHU Timone, Marseille, 13385 France.
Thromb Res. 2009 May;124(1):33-6. doi: 10.1016/j.thromres.2008.09.014. Epub 2008 Nov 5.
Increased doses of antiplatelet therapy have been proposed to overcome the variability of response. However, the chronic dose of aspirin after DES remains controversial.
We assessed in a prospective and randomized study the benefit of higher dose of aspirin, in association with clopidogrel, on aspirin response and non COX-specific platelet testing in patients receiving Drug Eluting Stent (DES) for stable angina pectoris. 50 consecutive patients receiving DES for stable angina pectoris were prospectively included. They received loading dose of 250 mg aspirin and 600 mg clopidogrel and antiplatelet response was assessed with Arachidonic Acid-induced aggregation (AA-Ag) and ADP-induced aggregation (ADP-Ag) for aspirin and clopidogrel response respectively. Patients were randomized to either 75 or 160 mg of aspirin with 150 mg clopidogrel and platelet testing were repeated one month after hospital discharge. The two groups (aspirin "75 mg" or "160 mg") had no difference for aspirin response: AA-Ag (5.2 +/- 1.7% vs 6 +/- 2%, p = 0.75) and non COX-specific pathway testing: ADP-Ag (47 +/- 3% vs 49 +/- 4%, p = 0.61).
The present study did not show any benefit of higher dose of aspirin neither on aspirin responsiveness, nor on inhibition of non COX-specific pathway. These data does not support use of higher dose than 75 mg of aspirin in association with clopidogrel in patients receiving DES, especially while higher doses have been associated with increased bleeding risk.
有人提出增加抗血小板治疗剂量以克服反应变异性。然而,药物洗脱支架(DES)置入术后阿司匹林的长期剂量仍存在争议。
我们进行了一项前瞻性随机研究,评估在接受DES治疗稳定型心绞痛的患者中,高剂量阿司匹林联合氯吡格雷对阿司匹林反应及非环氧化酶(COX)特异性血小板检测的益处。前瞻性纳入了50例连续接受DES治疗稳定型心绞痛的患者。他们接受了250mg阿司匹林和600mg氯吡格雷的负荷剂量,分别通过花生四烯酸诱导的聚集(AA-Ag)和ADP诱导的聚集(ADP-Ag)评估阿司匹林和氯吡格雷的抗血小板反应。患者被随机分为服用75mg或160mg阿司匹林联合150mg氯吡格雷,出院1个月后重复血小板检测。两组(阿司匹林“75mg”组或“160mg”组)在阿司匹林反应方面无差异:AA-Ag(5.2±1.7%对6±2%,p=0.75)以及非COX特异性途径检测:ADP-Ag(47±3%对49±4%,p=0.61)。
本研究未显示高剂量阿司匹林在阿司匹林反应性或非COX特异性途径抑制方面有任何益处。这些数据不支持在接受DES的患者中使用高于75mg的阿司匹林联合氯吡格雷,特别是鉴于高剂量与出血风险增加相关。