首页> 外文OA文献 >Efficacy and Safety of Cangrelor in Women Versus Men During Percutaneous Coronary Intervention: Insights From the Cangrelor versus Standard Therapy to Achieve Optimal Management of Platelet Inhibition (CHAMPION PHOENIX) Trial
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Efficacy and Safety of Cangrelor in Women Versus Men During Percutaneous Coronary Intervention: Insights From the Cangrelor versus Standard Therapy to Achieve Optimal Management of Platelet Inhibition (CHAMPION PHOENIX) Trial

机译:Cangrelor在经皮冠状动脉介入治疗中对女性与男性的疗效和安全性:来自Cangrelor与标准疗法的见解,以实现血小板抑制的最佳管理(CHampION pHOENIX)试验

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摘要

Background—Cangrelor is an intravenous ADP receptor antagonist that leads to potent and reversible inhibition of platelet aggregation. The relative safety and efficacy of some antiplatelet drugs in women has been disputed. Methods and Results—The Cangrelor versus Standard Therapy to Achieve Optimal Management of Platelet Inhibition (CHAMPION PHOENIX) trial randomized 11 145 patients undergoing elective or urgent percutaneous coronary intervention to cangrelor or clopidogrel. The primary efficacy end point was the composite of death, myocardial infarction, ischemia-driven revascularization, or stent thrombosis at 48 hours; the key secondary end point was stent thrombosis at 48 hours. The primary safety end point was GUSTO severe bleeding at 48 hours. Of subjects analyzed, 3051 (28%) were female. Cangrelor reduced the odds of the primary end point by 35% in women (adjusted odds ratio [OR], 0.65; 95% confidence interval [CI], 0.48–0.89) and by 14% in men (OR, 0.86; 95% CI, 0.70–1.05; P interaction=0.23) compared with clopidogrel. Cangrelor reduced the odds of stent thrombosis by 61% in women (OR, 0.39; 95% CI, 0.20–0.77) and 16% in men (OR, 0.84; 95% CI, 0.53–1.33; P interaction=0.11). The odds of severe bleeding were similar in both women and men treated with cangrelor (0.3% versus 0.2%, P=0.30 [women]; 0.1% versus 0.1%, P=0.41 [men]; P interaction=0.88) versus clopidogrel. Cangrelor increased the odds of moderate bleeding in women (0.9% versus 0.3%, P=0.02), but not in men (0.2% versus 0.2%, P=0.68; P interaction=0.040). The net clinical benefit (primary efficacy and safety end point) favored cangrelor in both women (OR, 0.68; 95% CI, 0.50–0.92) and men (OR, 0.87; 95% CI, 0.71–1.06; P interaction=0.26). Conclusions—In CHAMPION PHOENIX, cangrelor reduced the odds of major adverse cardiovascular events and stent thrombosis in women and men and appeared to offer greater net clinical benefit than clopidogrel.
机译:背景技术Cangrelor是一种静脉ADP受体拮抗剂,可有效且可逆地抑制血小板凝集。一些抗血小板药物在女性中的相对安全性和有效性一直存在争议。方法和结果-通过Cangrelor与标准疗法实现最佳血小板抑制治疗(CHAMPION PHOENIX)的研究,将11名145例接受选择性或紧急经皮冠状动脉介入治疗cangrelor或氯吡格雷的患者随机分组。主要疗效终点是48小时时死亡,心肌梗塞,缺血性血运重建或支架血栓形成的综合结果;关键的次要终点是48小时支架血栓形成。主要安全终点是在48小时内GUSTO严重出血。在分析的受试者中,3051(28%)是女性。 Cangrelor降低了女性主要终点的几率35%(调整后的优势比[OR],0.65; 95%的置信区间[CI],0.48-0.89),男性降低了14%(OR,0.86; 95%CI) (0.70–1.05; P交互作用= 0.23)与氯吡格雷相比。 Cangrelor将女性支架内血栓形成的几率降低了61%(OR,0.39; 95%CI,0.20-0.77),男性降低了16%(OR,0.84; 95%CI,0.53-1.33; P相互作用= 0.11)。与氯吡格雷相比,接受坎格雷洛治疗的男女严重出血的几率相似(0.3%vs 0.2%,P = 0.30 [女性]; 0.1%vs 0.1%,P = 0.41 [男性]; P相互作用= 0.88)。坎格雷洛增加了女性中度出血的几率(0.9%比0.3%,P = 0.02),而男性则没有(0.2%比0.2%,P = 0.68; P交互作用= 0.040)。男性(OR,0.68; 95%CI,0.50-0.92)和男性(OR,0.87; 95%CI,0.71-1.06; P交互作用= 0.26)对坎格雷洛的临床疗效(主要疗效和安全性终点)均偏爱坎格雷洛。结论—在Champion Phoenix中,cangrelor降低了男性和女性发生重大心血管不良事件和支架血栓的几率,并提供了比氯吡格雷更大的净临床收益。

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