Mehta Shamir R, Bassand Jean-Pierre, Chrolavicius Susan, Diaz Rafael, Fox Keith A A, Granger Christopher B, Jolly Sanjit, Rupprecht Hans-Jurgen, Widimsky Petr, Yusuf Salim
McMaster University and the Population Health Research Institute, Hamilton Health Sciences, Hamilton, Ontario, Canada.
Am Heart J. 2008 Dec;156(6):1080-1088.e1. doi: 10.1016/j.ahj.2008.07.026. Epub 2008 Nov 1.
Antiplatelet therapy with clopidogrel and acetylsalicylic acid (ASA) reduces major cardiovascular events in patients with ST and non-ST-segment-elevation acute coronary syndromes (ACS). Recent mechanistic and clinical data suggest that higher loading and maintenance doses of clopidogrel may achieve a more rapid and greater degree of platelet inhibition that translates into improved clinical outcomes, but this is yet to be formally evaluated in an adequately powered randomized trial.
To evaluate the efficacy and safety of (1) a higher loading and initial maintenance dose of clopidogrel compared with the standard-dose regimen and (2) high-dose ASA compared with low-dose ASA in patients with ST or non-ST-segment-elevation ACS managed with an early invasive strategy.
Multicenter, international, randomized, 2 x 2 factorial design trial evaluating a clopidogrel high-dose regimen (600 mg loading dose on day 1 followed by 150 mg once daily on days 2 to 7, followed by 75 mg once daily on days 8-30) compared with the standard-dose regimen (300 mg loading dose on day 1, followed by 75 mg once daily on days 2-30) and high-dose ASA (300-325 mg daily) versus low-dose ASA (75-100 mg daily) in patients with ST or non-ST-segment-elevation ACS managed with an early invasive strategy. The clopidogrel dose comparison is double-blind and the ASA dose comparison is open-label. The primary outcome is the composite of death from cardiovascular causes, myocardial (re)infarction or stroke up to day 30. The primary safety outcome is major bleeding. The sample size is 18,000 to 20,000 patients.
The CURRENT-OASIS 7 trial will help to define optimal dosing regimens for clopidogrel and ASA in patients with ST and non-ST-segment-elevation ACS treated with an early invasive strategy.
氯吡格雷与阿司匹林联合抗血小板治疗可降低ST段抬高型和非ST段抬高型急性冠状动脉综合征(ACS)患者的主要心血管事件发生率。近期的机制研究和临床数据表明,更高的氯吡格雷负荷剂量和维持剂量可能实现更快、更强的血小板抑制,从而改善临床结局,但这一点尚未在一项足够大规模的随机试验中得到正式评估。
评估在采用早期侵入性策略治疗的ST段抬高或非ST段抬高型ACS患者中,(1)与标准剂量方案相比,更高的氯吡格雷负荷剂量和初始维持剂量;(2)与低剂量阿司匹林相比,高剂量阿司匹林的疗效和安全性。
多中心、国际性、随机、2×2析因设计试验,评估氯吡格雷高剂量方案(第1天负荷剂量600mg,随后第2至7天每日150mg,第8至30天每日75mg)与标准剂量方案(第1天负荷剂量300mg,随后第2至30天每日75mg)以及高剂量阿司匹林(每日300 - 325mg)与低剂量阿司匹林(每日75 - 100mg)在采用早期侵入性策略治疗的ST段抬高或非ST段抬高型ACS患者中的疗效。氯吡格雷剂量比较为双盲,阿司匹林剂量比较为开放标签。主要结局是至第30天心血管原因死亡、心肌(再)梗死或卒中的复合终点。主要安全性结局是大出血。样本量为18000至20000例患者。
CURRENT - OASIS 7试验将有助于确定在采用早期侵入性策略治疗的ST段抬高和非ST段抬高型ACS患者中氯吡格雷和阿司匹林的最佳给药方案。