Department of Clinical Pharmacology, Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
State Key Laboratory of Drug Delivery Technology and Pharmacokinetics, Tianjin Institute of Pharmaceutical Research, Tianjin, China.
Clin Ther. 2019 Jun;41(6):1097-1109. doi: 10.1016/j.clinthera.2019.04.006. Epub 2019 May 1.
The combination of warfarin and compound Danshen dripping pill (CDDP) is helpful for patients with both coronary heart disease (CHD) and atrial fibrillation (AF). The main adverse drug reaction of warfarin is bleeding because of its narrow therapeutic index. The safety of a combination therapy with warfarin and CDDP is always a concern. Our previous research showed that the combination of warfarin and CDDP improved the quality of life for patients with both CHD and AF. This study describes the changes in dose and concentration of warfarin necessary and evaluates bleeding risk when warfarin is given concomitantly with CDDP.
An ultra-performance liquid chromatography-MS/MS method with a chiral column was developed to assay the concentration of S-warfarin and R-warfarin in human plasma simultaneously. The method was applied to compare the concentration of warfarin in patients taking warfarin combined with CDDP and without CDDP. International normalized ratio (INR) values were monitored to evaluate bleeding risk. Paired t tests were then used to compare the dose and the concentration in 2 periods. Moreover, patients with VKORC1, CYP2C9*3, CYP4F2, EPHX1, and PROC gene polymorphisms were evaluated to determine interactions.
The results indicate that the dose of warfarin had no significant change with or without CDDP. Also, the peak concentrations of S-warfarin and total warfarin were significantly different in CYP4F2 C/C patients, but there was no significant difference identified in other genetic groups. No bleeding occurred in the study.
The dose of warfarin would be sustainable when combined with CDDP, because CDDP did not affect concentration of warfarin significantly in most patients and the change of INR was not significant.
ChiCTR-ONRC-13003523.
华法林与复方丹参滴丸联合应用有助于冠心病(CHD)合并心房颤动(AF)患者。华法林主要的不良反应是出血,因其治疗指数较窄。华法林与复方丹参滴丸联合治疗的安全性一直备受关注。我们之前的研究表明,华法林与复方丹参滴丸联合应用可改善 CHD 合并 AF 患者的生活质量。本研究描述了华法林与复方丹参滴丸合用所需的剂量和浓度变化,并评估了出血风险。
建立了一种超高效液相色谱-串联质谱法(UPLC-MS/MS),并用手性柱同时测定人血浆中 S-华法林和 R-华法林的浓度。该方法用于比较服用华法林联合和不联合复方丹参滴丸的患者的华法林浓度。监测国际标准化比值(INR)值以评估出血风险。然后使用配对 t 检验比较两个时期的剂量和浓度。此外,还评估了 VKORC1、CYP2C9*3、CYP4F2、EPHX1 和 PROC 基因多态性的患者,以确定相互作用。
结果表明,华法林的剂量在联合或不联合复方丹参滴丸时没有显著变化。此外,CYP4F2 C/C 患者的 S-华法林和总华法林的峰值浓度有显著差异,但在其他基因组中未发现显著差异。研究中未发生出血。
当与复方丹参滴丸联合使用时,华法林的剂量可能是可持续的,因为在大多数患者中,复方丹参滴丸不会显著影响华法林的浓度,INR 的变化也不显著。
ChiCTR-ONRC-13003523。