Département de Cardiologie, CHU Timone, Marseille, France.
JACC Cardiovasc Interv. 2013 Aug;6(8):854-63. doi: 10.1016/j.jcin.2013.04.009.
This study was designed to define the hyperresponse to thienopyridine (very low on-treatment platelet reactivity [VLTPR]) as the most predictive threshold value of platelet reactivity index vasodilator-stimulated phosphoprotein (PRI VASP) for the prediction of non-access site-related bleeding events. We also aimed to identify predictors of bleeding and VLTPR in patients treated with thienopyridines.
New P2Y12 blockers and platelet monitoring has been proposed to optimize platelet inhibition after acute coronary syndromes and improve ischemic outcomes. However, bleeding complications remain the Achilles' heel of antiplatelet therapy, and platelet monitoring could be useful to evaluate this risk.
A total of 1,542 consecutive patients undergoing coronary stenting for ACS were included in the present study (287 taking clopidogrel 75 mg, 868 taking clopidogrel 150 mg, and 387 taking prasugrel 10 mg).
During 6-month follow-up, 9% of patients (n = 139) experienced nonaccess site-related Bleeding Academic Research Consortium bleeding complications. These patients were more often women and nondiabetic and had lower PRI VASP values than others (p < 0.001). Receiver-operating characteristic curve analysis (0.71, p < 0.01) identified a threshold value for VLTPR of PRI VASP ≤10% to predict bleeding events with a sensitivity of 17% and a specificity of 97%. Although prasugrel was the main predictor of VLTPR in the whole population (odds ratio: 10.2, 95% confidence interval: 3.0 to -34.2; p < 0.001), VLTPR was the strongest and independent predictor of bleeding (odds ratio: 4.7, 95% confidence interval: 2.7 to 8.3; p < 0.001).
The present study identified VLTPR (PRI VASP ≤10%) as the strongest predictor of bleeding complications in patients treated with thienopyridines. This marker could be useful for tailored therapy and bleeding prevention.
本研究旨在将噻吩吡啶的高反应(极低的治疗后血小板反应性 [VLTPR])定义为血小板反应指数血管扩张刺激磷酸蛋白(PRI VASP)预测非介入部位相关出血事件的最具预测价值的阈值。我们还旨在确定接受噻吩吡啶治疗的患者出血和 VLTPR 的预测因素。
新的 P2Y12 抑制剂和血小板监测已被提出用于优化急性冠脉综合征后的血小板抑制作用并改善缺血结局。然而,出血并发症仍然是抗血小板治疗的阿喀琉斯之踵,血小板监测可能有助于评估这种风险。
本研究共纳入 1542 例因 ACS 行冠状动脉支架置入术的连续患者(287 例服用氯吡格雷 75mg,868 例服用氯吡格雷 150mg,387 例服用普拉格雷 10mg)。
在 6 个月的随访期间,9%的患者(n=139)发生了非介入部位相关的出血学术研究联合会出血并发症。这些患者更常为女性和非糖尿病患者,且 PRI VASP 值低于其他患者(p<0.001)。受试者工作特征曲线分析(0.71,p<0.01)确定了 PRI VASP 中 VLTPR 的截断值≤10%,以预测出血事件,其敏感性为 17%,特异性为 97%。尽管普拉格雷是整个人群中 VLTPR 的主要预测因素(优势比:10.2,95%置信区间:3.0 至-34.2;p<0.001),但 VLTPR 是出血的最强和独立预测因素(优势比:4.7,95%置信区间:2.7 至 8.3;p<0.001)。
本研究确定了 VLTPR(PRI VASP≤10%)是接受噻吩吡啶治疗的患者出血并发症的最强预测因素。该标志物可用于个体化治疗和出血预防。