Department of Community Medicine and Epidemiology, Lady Davis Carmel Medical Center, Clalit Health Services, Haifa, Israel.
Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Clin Pharmacol Ther. 2021 Dec;110(6):1526-1536. doi: 10.1002/cpt.2369. Epub 2021 Aug 10.
Concomitant use of direct oral anticoagulants (DOACs) and medications with inhibition/induction effect on P-gp/CYP3A might increase risk of bleeding/treatment failure, respectively. We designed a nested case-control study within a Clalit cohort of patients with atrial fibrillation (AF) and a cohort of patients with venous thromboembolism, new users of a DOAC (January 1, 2010 to August 24, 2020). Propensity scores were constructed from demographic/clinical characteristics, and medications at cohort entry. Each case of: (i) serious bleeding event; (ii) stroke/systemic emboli (SE) in patients with AF; (iii) recurrent thromboembolism in patients with thromboembolism, was matched by age, sex, length of follow-up, year of cohort entry, DOAC type, and DOAC indication, to up to 20 controls. Within 89,284 patients with AF and venous thromboembolism and 126,302 patient-years of follow-up, there were 1,587 serious bleeding events. Risk of serious bleeding increased in association with concurrent prescription of P-gp/CYP3A4 inhibitors. Specifically, higher bleeding risk was associated with dabigatran-verapamil, rivaroxaban-verapamil, and rivaroxaban-amiodarone concurrent prescriptions: adjusted odds ratios (ORs) 2.29 (1.13-4.60), 2.18 (1.07-4.40), and 1.68 (1.14-2.49), respectively. There were 1,116 events of stroke/SE, in 79,302 DOAC-treated patients with AF and 118,124 patient-years of follow-up. Concomitant use of phenytoin, carbamazepine, valproic acid, or levetiracetam was associated with risk for stroke/SE: adjusted OR 2.18 (1.55-3.10). Risk of recurrent venous thromboembolism could not be assessed due to the low number of cases. Concurrent prescriptions of dabigatran or rivaroxaban with verapamil, and of rivaroxaban with amiodarone, are associated with increased risk for serious bleeding. Higher risk for stroke/SE in patients with AF is associated with concurrent prescriptions of DOACs with phenytoin, carbamazepine, valproic acid, or levetiracetam.
同时使用直接口服抗凝剂(DOAC)和对 P-糖蛋白/细胞色素 3A 具有抑制/诱导作用的药物可能分别增加出血/治疗失败的风险。我们在 Clalit 心房颤动(AF)患者队列和静脉血栓栓塞患者队列中设计了一个嵌套病例对照研究,新使用 DOAC(2010 年 1 月 1 日至 2020 年 8 月 24 日)。从人口统计学/临床特征和队列入组时的药物中构建倾向评分。AF 患者的:(i)严重出血事件;(ii)中风/全身性栓塞(SE);(iii)血栓栓塞患者的复发性血栓栓塞,分别与年龄、性别、随访时间、队列入组年份、DOAC 类型和 DOAC 适应症相匹配,最多匹配 20 名对照。在 89284 名 AF 和静脉血栓栓塞患者和 126302 患者年的随访中,有 1587 例严重出血事件。同时处方 P-糖蛋白/细胞色素 3A4 抑制剂与严重出血风险增加相关。具体而言,与达比加群-维拉帕米、利伐沙班-维拉帕米和利伐沙班-胺碘酮同时处方相关的出血风险更高:调整后的比值比(OR)分别为 2.29(1.13-4.60)、2.18(1.07-4.40)和 1.68(1.14-2.49)。在 79302 例接受 AF DOAC 治疗的患者和 118124 患者年的随访中,有 1116 例发生中风/SE。同时使用苯妥英钠、卡马西平、丙戊酸或左乙拉西坦与中风/SE 风险相关:调整后的 OR 为 2.18(1.55-3.10)。由于病例数量较少,无法评估复发性静脉血栓栓塞的风险。达比加群或利伐沙班与维拉帕米同时处方,以及利伐沙班与胺碘酮同时处方,与严重出血风险增加相关。AF 患者中风/SE 风险增加与 DOAC 与苯妥英钠、卡马西平、丙戊酸或左乙拉西坦同时处方相关。