Morath Benedict, Foerster Kathrin I, Chiriac Ute, Zaradzki Marcin, Hoppe-Tichy Torsten, Schrey David, Burhenne Jürgen, Czock David, Karck Matthias, Haefeli Walter E, Wicha Sebastian G
Hospital Pharmacy, Heidelberg University Hospital, Im Neuenheimer Feld 670, 69120, Heidelberg, Germany.
Internal Medicine IX, Department of Clinical Pharmacology and Pharmacoepidemiology, Heidelberg University Hospital, Heidelberg, Germany.
Clin Pharmacokinet. 2025 Jun 5. doi: 10.1007/s40262-025-01534-z.
To investigate the effect of amiodarone on apixaban pharmacokinetics in cardiac surgery patients with postoperative atrial fibrillation.
Apixaban concentrations of postoperative cardiac surgery patients with or without amiodarone therapy were quantified using liquid chromatography-tandem mass spectrometry (LC-MS/MS) in clinical routine. A population pharmacokinetic model was built using nonlinear mixed effects modeling in NONMEM 7.5 using first-order conditional estimation with interaction. The impact of amiodarone and creatinine clearance (CrCL) on apixaban exposure under various dosing regimens was analyzed using Simulx (Lixoft).
A total of 33 patients with 76 apixaban concentrations were included. A one-compartment model best described the pharmacokinetics of apixaban with a clearance (CL/F) of 3.05 L/h, apparent volume of distribution (V/F) of 23.7 L, and an absorption rate constant (k) of 0.652/h. Interindividual variability (IIV) was observed in CL/F but not in V/F and k. The covariates amiodarone and CrCL were independently associated with apixaban CL/F. Under concomitant amiodarone therapy, simulations predicted an increase of 44-49% in apixaban area under the concentration-time curve (AUC), and AUC nearly doubled at CrCL 35 mL/min. A dose of 2.5 mg apixaban twice daily (b.i.d.) was identified as a potential dosing option in the CrCL range of 15-50 mL/min under amiodarone comedication.
Concomitant amiodarone therapy reduced apixaban CL/F and increased the risk of high exposure in patients with impaired renal function. A dose of 2.5 mg apixaban b.i.d. for a CrCL range of 30-50 mL/min under concomitant amiodarone therapy was identified as a new dosing option.
研究胺碘酮对心脏手术后发生房颤的患者中阿哌沙班药代动力学的影响。
在临床常规中,使用液相色谱 - 串联质谱法(LC-MS/MS)对接受或未接受胺碘酮治疗的心脏手术后患者的阿哌沙班浓度进行定量。使用NONMEM 7.5中的非线性混合效应模型,采用带交互作用的一阶条件估计法建立群体药代动力学模型。使用Simulx(Lixoft)分析胺碘酮和肌酐清除率(CrCL)在各种给药方案下对阿哌沙班暴露的影响。
共纳入33例患者,有76个阿哌沙班浓度数据。单室模型能最好地描述阿哌沙班的药代动力学,清除率(CL/F)为3.05 L/h,表观分布容积(V/F)为23.7 L,吸收速率常数(k)为0.652/h。在CL/F中观察到个体间变异性(IIV),但在V/F和k中未观察到。协变量胺碘酮和CrCL与阿哌沙班CL/F独立相关。在胺碘酮伴随治疗下,模拟预测阿哌沙班浓度 - 时间曲线下面积(AUC)增加44% - 49%,当CrCL为35 mL/min时,AUC几乎翻倍。在胺碘酮联合用药的情况下,对于CrCL在15 - 50 mL/min范围内,每日两次服用2.5 mg阿哌沙班被确定为一种潜在的给药方案。
胺碘酮伴随治疗降低了阿哌沙班CL/F,并增加了肾功能受损患者高暴露的风险。在胺碘酮伴随治疗下,对于CrCL范围为30 - 50 mL/min的患者,每日两次服用2.5 mg阿哌沙班被确定为一种新的给药方案。