Memorial Hermann-Texas Medical Center, Houston, TX, USA.
Ann Pharmacother. 2014 May;48(5):644-7. doi: 10.1177/1060028013520140. Epub 2014 Jan 29.
To report the influence of phenytoin on the antiplatelet effects of ticagrelor using a validated platelet aggregation study.
A 71-year-old man with coronary artery disease underwent percutaneous coronary intervention to revascularize several major coronary arteries. The patient was previously on phenytoin and was initiated on ticagrelor for antiplatelet therapy following stent placement. While the patient was receiving both drugs, platelet aggregation studies revealed less platelet inhibition than would be expected in a patient not taking a concomitant inducer of ticagrelor metabolism. On discontinuation of phenytoin, platelet inhibition improved.
Dual antiplatelet therapy with aspirin and a P2Y12 receptor antagonist following placement of coronary stents is critical to prevent stent thrombosis and subsequent myocardial infarction. Ticagrelor is a recently approved P2Y12 receptor antagonist that is subject to drug-drug interactions involving the hepatic cytochrome P450-3A4 enzyme system because of its metabolic elimination pathway. This case demonstrates ticagrelor's drug-drug interaction with phenytoin through a platelet aggregation study and supports the manufacturer recommendation to avoid the combination of ticagrelor with any known inducers of cytochrome P450-3A4 metabolism.
The combination of ticagrelor and phenytoin may represent a potentially clinically significant drug-drug interaction because of phenytoin induction of ticagrelor metabolism and reduced P2Y12 receptor inhibition in patients who have recently undergone percutaneous coronary intervention and cardiac stent placement.
使用经过验证的血小板聚集研究报告苯妥英对替格瑞洛抗血小板作用的影响。
一名 71 岁男性患有冠状动脉疾病,进行了经皮冠状动脉介入治疗以重新开通几条主要冠状动脉。该患者之前服用苯妥英,并在支架放置后开始服用替格瑞洛进行抗血小板治疗。在患者同时接受这两种药物治疗时,血小板聚集研究显示血小板抑制作用不如未服用替格瑞洛代谢诱导剂的患者预期的那样。停用苯妥英后,血小板抑制作用得到改善。
在放置冠状动脉支架后,联合使用阿司匹林和 P2Y12 受体拮抗剂进行双重抗血小板治疗对于预防支架血栓形成和随后的心肌梗死至关重要。替格瑞洛是一种最近批准的 P2Y12 受体拮抗剂,由于其代谢消除途径,涉及肝细胞色素 P450-3A4 酶系统,它会发生药物相互作用。该病例通过血小板聚集研究证明了替格瑞洛与苯妥英的药物相互作用,并支持制造商的建议,即避免替格瑞洛与任何已知的细胞色素 P450-3A4 代谢诱导剂联合使用。
替格瑞洛和苯妥英的联合使用可能代表一种潜在的临床显著的药物相互作用,因为苯妥英诱导替格瑞洛代谢,以及最近接受经皮冠状动脉介入治疗和心脏支架放置的患者 P2Y12 受体抑制作用降低。