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首页> 外文期刊>Frontiers in Pharmacology >Comparative Long-Term Effect of Three Anti-P2Y12 Drugs after Percutaneous Angioplasty: An Observational Study Based on Electronic Drug Adherence Monitoring
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Comparative Long-Term Effect of Three Anti-P2Y12 Drugs after Percutaneous Angioplasty: An Observational Study Based on Electronic Drug Adherence Monitoring

机译:三种抗P2Y12药物经皮血管成形术后的远期效果比较:基于电子药物粘附监测的观察性研究

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Aims: Dual platelet inhibition using anti-P2Y12 drugs and aspirin is the standard of care in patients after percutaneous coronary interventions (PCI). Prasugrel and ticagrelor have been shown to be more potent than clopidogrel with less high on-treatment platelet reactivity. Whether differences in long-term adherence to these drugs can partly explain different antiplatelet efficacy has not been studied so far. The objective was to compare the long-term P2Y12 receptor inhibition and drug adherence to different anti-P2Y12 drugs, and to assess the impact of adherence on the pharmacodynamic effect. Methods: Monocentric, prospective, observational study. Stable outpatients treated with clopidogrel 75 mg once daily, prasugrel 10 mg once daily or ticagrelor 90 mg twice daily after PCI with stent implantation were included. Drug adherence was recorded during 6 months using electronic monitoring. Platelet responsiveness was assessed with the vasodilator-stimulated phosphoprotein platelet reactivity index (VASP-PRI) at inclusion, 3 and 6 months. Results: 120 patients had VASP-PRI and adherence data available. At 6-months, mean VASP-PRI (±SD) was 17.7 ± 11.0% with ticagrelor, 29.2 ± 15.5% with prasugrel and 47.2 ± 17.6% with clopidogrel (ANOVA, P < 0.0001).Median [IQR] taking adherence was 96 [82–100]% with ticagrelor, 100 [97–101]% with prasugrel and 100 [99–101]% with clopidogrel ( p = 0.0001). Median [IQR] correct dosing was 88 [73–95]% with ticagrelor, 97 [92.5–98]% with prasugrel and 98 [96–99]% with clopidogrel ( p = 0.0001).Anti-P2Y12 drug ( p ≤ 0.001) and diabetes ( p = 0.014) emerged as predictors of poor antiplatelet response after adjusting for age, BMI, sex, and CYP2C19~(?)2 carriers status. Conclusion: Drug adherence to anti-P2Y12 drugs assessed with electronic monitoring was very high. However, anti-P2Y12 drugs showed significant differences in antiplatelet activity, with newer anti-P2Y12 drugs ticagrelor and prasugrel exerting a stronger P2Y12 receptor inhibition.These data suggest that pharmacokinetic-pharmacodynamic differences between oral anti-P2Y12 drugs are more important than adherence in determining antiplatelet efficacy when adherence to prescription is high.The study was registered (Current Controlled Trials ISRCTN85949729).
机译:目的:使用抗P2Y12药物和阿司匹林双重抑制血小板,是经皮冠状动脉介入治疗(PCI)后患者的标准护理。已显示普拉格雷和替卡格雷比氯吡格雷更有效,治疗时血小板反应性较低。到目前为止,尚未研究长期坚持使用这些药物的差异能否部分解释抗血小板药效的不同。目的是比较长期P2Y12受体抑制和药物对不同抗P2Y12药物的依从性,并评估依从性对药效的影响。方法:单中心,前瞻性,观察性研究。包括在支架植入后行PCI的氯吡格雷75 mg /天,普拉格雷10 mg /天或ticagrelor 90 mg /天2次的稳定门诊患者。使用电子监测记录6个月内的药物依从性。用血管舒张剂刺激的磷蛋白血小板反应性指数(VASP-PRI)在入选后3个月和6个月评估血小板反应性。结果:120例患者具有VASP-PRI和依从性数据。在6个月时,替卡格雷的平均VASP-PRI(±SD)为17.7±11.0%,普拉格雷的平均VASP-PRI为29.2±15.5%,氯吡格雷的平均VASP-PRI为47.2±17.6%(ANOVA,P <0.0001)。接受治疗的中位[IQR]为96替格瑞洛[82–100]%,普拉格雷100 [97–101]%和氯吡格雷100 [99–101]%(p = 0.0001)。替格瑞洛[IQR]正确剂量的中位数为88 [73-95]%,普拉格雷为97 [92.5-98]%,氯吡格雷为98 [96-99]%(p = 0.0001)。抗P2Y12药物(p≤0.001 ),糖尿病(p = 0.014)在调整了年龄,BMI,性别和CYP2C19〜(?)2携带者状态后成为抗血小板反应不良的预测指标。结论:通过电子监测评估的抗P2Y12药物依从性很高。然而,抗P2Y12药物在抗血小板活性方面表现出显着差异,新的抗P2Y12药物替卡格雷或普拉格雷对P2Y12受体的抑制作用更强,这些数据表明口服抗P2Y12药物之间的药代动力学药效学差异比依从性更重要。遵守处方时抗血小板药效高。该研究已注册(现行对照试验ISRCTN85949729)。

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