Szymanski Thomas W, Rockhold Matthew R, Lacoste Jordan L
Department of Pharmacy, WVU Medicine, Morgantown, WV, USA.
J Pharm Pract. 2025 Feb;38(1):204-207. doi: 10.1177/08971900241273095. Epub 2024 Aug 15.
Ticagrelor is contraindicated in combination with cytochrome P450 3A4 and 3A5 enzyme (CYP3A4/5) inducers due to increased clearance, causing diminished antiplatelet effects. The emergent nature of acute coronary syndromes (ACS) may preclude scrutinization of home medications before P2Y inhibitor administration. The purpose of this case series is to establish the temporal impact of CYP3A4/5 enzyme induction on ticagrelor's pharmacodynamic effect by utilizing VerifyNow platelet aggregation studies. This was a retrospective case series of three patients who were taking a CYP3A4/5-inducing medication and loaded with ticagrelor for ACS. The duration of ticagrelor's antiplatelet effect was dramatically shortened in the presence of background CYP3A4/5 induction. The offset of antiplatelet effect, defined by platelet reactivity units (PRU), was 10-24 hours in the presence of CYP3A4/5 enzyme induction compared to the anticipated 36-48 hours. This was consistent across CYP3A4/5-inducing medications including carbamazepine, phenobarbital, and phenytoin. This study demonstrates rapid return of platelet function after a ticagrelor loading dose in the presence of CYP3A4/5-inducing medications. Monitoring of PRU every 6-12 hours with subsequent loading with clopidogrel or prasugrel should be considered. Larger scale studies are warranted to confirm these results.
由于清除率增加会导致抗血小板作用减弱,替格瑞洛禁止与细胞色素P450 3A4和3A5酶(CYP3A4/5)诱导剂联合使用。急性冠状动脉综合征(ACS)的紧急性质可能使在给予P2Y抑制剂之前无法仔细检查家庭用药。本病例系列的目的是通过使用VerifyNow血小板聚集研究来确定CYP3A4/5酶诱导对替格瑞洛药效学作用的时间影响。这是一个回顾性病例系列,包含三名正在服用CYP3A4/5诱导药物并因ACS而负荷替格瑞洛的患者。在存在背景CYP3A4/5诱导的情况下,替格瑞洛的抗血小板作用持续时间显著缩短。与预期的36 - 48小时相比,在存在CYP3A4/5酶诱导的情况下,由血小板反应性单位(PRU)定义的抗血小板作用消退时间为10 - 24小时。在包括卡马西平、苯巴比妥和苯妥英在内的CYP3A4/5诱导药物中均是如此。本研究表明,在存在CYP3A4/5诱导药物的情况下,替格瑞洛负荷剂量后血小板功能会迅速恢复。应考虑每6 - 12小时监测PRU,随后负荷氯吡格雷或普拉格雷。需要进行更大规模的研究来证实这些结果。