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Implementation and evaluation of a CYP2C19 genotype-guided antiplatelet therapy algorithm in high-risk coronary artery disease patients

机译:CYP2C19基因型指导的抗血小板治疗算法在高危冠心病患者中的实施和评估

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Aim: An algorithm that uses clinical factors and CYP2C19 genotype to guide P2Y(12) inhibitor selection in high-risk patients undergoing percutaneous coronary intervention was implemented at our institution. We sought to evaluate use of this algorithm and identify which factors influenced P2Y(12) inhibitor selection. Patients & methods: This retrospective cohort study included 264 patients receiving percutaneous coronary intervention from July-December 2012. Results: CYP2C19 genotype was obtained in 229 patients; of these, 30% were intermediate or poor metabolizers. CYP2C19 intermediate or poor metabolizer phenotype was among the strongest predictors for selecting prasugrel or ticagrelor as maintenance therapy (p < 0.001), and was the only significant predictor of a change in therapy (p < 0.001). Conclusion: These findings suggest that using CYP2C19 genotype to guide P2Y(12) inhibitor selection is feasible.
机译:目的:在我院实施了一种算法,该算法利用临床因素和CYP2C19基因型指导经皮冠状动脉介入治疗的高危患者选择P2Y(12)抑制剂。我们试图评估该算法的使用并确定哪些因素影响了P2Y(12)抑制剂的选择。患者与方法:这项回顾性队列研究包括2012年7月至12月接受264例经皮冠状动脉介入治疗的患者。结果:229例患者获得了CYP2C19基因型。其中,30%是中度或弱代谢者。 CYP2C19中度或不良代谢者表型是选择普拉格雷或替卡格雷作为维持治疗的最强预测指标之一(p <0.001),并且是治疗改变的唯一重要预测指标(p <0.001)。结论:这些发现表明使用CYP2C19基因型指导P2Y(12)抑制剂的选择是可行的。

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