Gao Yan, Huang Qingsong, Li Jun, He Junsheng, Qian Fang, Yi Juanjuan
Department of Pharmacy, Shanghai Jiading District Hospital of Traditional Chinese Medicine, Shanghai, China.
Department of Internal Medicine, Shanghai Jiading District Hospital of Traditional Chinese Medicine, Shanghai, China.
Front Pharmacol. 2024 Nov 29;15:1418997. doi: 10.3389/fphar.2024.1418997. eCollection 2024.
This study aims to examine the unresolved drug-drug interactions of warfarin using real-world data.
Electronic medical records from a hospital in Shanghai, China, were used to summarize drug-related problems (DRPs) among inpatients taking warfarin in 2022. Additionally, adverse event data for warfarin from January 2004 to December 2023 were extracted from the U.S. adverse event reporting system to evaluate the bleeding risk associated with the concomitant use of warfarin and COVID-19 Vaccine/drugs, monoclonal antibodies, and targeted anticancer agents.
The electronic clinical records yielded 180 cases, of which 130 cases (72.22%) had 276 DRPs identified. DRP5 (n = 172, 62.32%) was identified as the most common issue, comprising 145 drug interactions and 27 adverse drug reactions (ADRs). The analyses of warfarin ADR records (n = 53,709) from the database revealed that tocilizumab (adjusted Odds Ratio (aOR): 3.39 [95% CI: 1.77-7.03]; < 0.001), ibrutinib (aOR: 2.53 [1.61-4.19]; < 0.001), and cabozantinib (aOR: 3.34 [1.40-9.85]; = 0.013) significantly increased the risk of warfarin bleeding. In contrast, nirmatrelvir-ritonavir (aOR: 0.32 [0.14-0.69]; = 0.004), adalimumab (aOR: 0.72 [0.56-0.93]; = 0.012), golimumab (aOR: 0.18 [0.05-0.50]; = 0.002), tofacitinib (aOR: 0.51 [0.29-0.86]; = 0.013), and dabrafenib (aOR: 0.17 [0.04-0.55]; = 0.007) significantly reduced the risk of bleeding when combined with warfarin. Remdesivir combined with warfarin was associated with a statistically significant increase in bleeding events ( = 0.047); while the risk was not significant after adjusting for age and sex (aOR: 1.79; = 0.2). No significant effect was observed with the COVID-19 vaccine (aOR: 0.89; = 0.8).
Drug-drug interactions contribute to the adverse effects of warfarin. This study provides real-world evidence of newly identified drug interactions with warfarin. It reminds clinicians to monitor INR and adjust warfarin doses accordingly when used in combination with these medications.
本研究旨在利用真实世界数据检查华法林未解决的药物相互作用。
使用中国上海一家医院的电子病历总结2022年服用华法林的住院患者中的药物相关问题(DRP)。此外,从美国不良事件报告系统中提取2004年1月至2023年12月华法林的不良事件数据,以评估华法林与新冠疫苗/药物、单克隆抗体和靶向抗癌药联合使用时的出血风险。
电子临床记录产生了180例病例,其中130例(72.22%)有276个已识别的DRP。DRP5(n = 172,62.32%)被确定为最常见问题,包括145种药物相互作用和27种药物不良反应(ADR)。对数据库中华法林ADR记录(n = 53,709)的分析显示,托珠单抗(调整后比值比(aOR):3.39 [95%置信区间:1.77 - 7.03];P < 0.001)、伊布替尼(aOR:2.53 [1.61 - 4.19];P < 0.001)和卡博替尼(aOR:3.34 [1.40 - 9.85];P = 0.013)显著增加了华法林出血风险。相比之下,奈玛特韦 - 利托那韦(aOR:0.32 [0.14 - 0.69];P = 0.004)、阿达木单抗(aOR:0.72 [0.56 - 0.93];P = 0.012)、戈利木单抗(aOR:0.18 [0.05 - 0.50];P = 0.002)、托法替布(aOR:0.51 [0.29 - 0.86];P = 0.013)和达拉非尼(aOR:0.17 [0.04 - 0.55];P = 0.007)与华法林联合使用时显著降低了出血风险。瑞德西韦与华法林联合使用与出血事件的统计学显著增加相关(P = 0.047);而在调整年龄和性别后风险不显著(aOR:1.79;P = 0.2)。新冠疫苗未观察到显著影响(aOR:0.89;P = 0.8)。
药物相互作用导致了华法林的不良反应。本研究提供了新发现的与华法林药物相互作用的真实世界证据。它提醒临床医生在与这些药物联合使用时监测国际标准化比值(INR)并相应调整华法林剂量。