INSERM UMR738, University Paris Diderot, Paris, France.
Clin Pharmacol Ther. 2012 May;91(5):777-86. doi: 10.1038/clpt.2011.309.
In the PREPA observational study, we investigated the factors influencing pharmacokinetic and pharmacodynamic variability in the responses to fluindione, an oral anticoagulant drug, in a general population of octogenarian inpatients.Measurements of fluindione concentrations and international normalized ratio (INR ) were obtained for 131 inpatients in whom fluindione treatment was initiated. Treatment was adjusted according to routine clinical practice. The data were analyzed using nonlinear mixed-effects modeling, and the parameters were estimated using MONOLI X 3.2. The pharmacokinetics (PK) of fluindione was monocompartmental, whereas the evolution of INR was modeled in accordance with a turnover model (inhibition of vitamin K recycling). Interindividual variability (II V) was very large. Clearance decreased with age and with prior administration of cordarone. Patients who had undergone surgery before the study had lower IC50 values, leading to an increased sensitivity to fluindione. Pharmacokinetic exposure is substantially increased in elderly patients, warranting a lower dose of fluindione.
在 PREPA 观察性研究中,我们调查了影响口服抗凝药物 fluindione 反应的药代动力学和药效动力学变异性的因素,该研究纳入了一般人群的 80 岁以上住院患者。我们对 131 名开始 fluindione 治疗的住院患者进行 fluindione 浓度和国际标准化比值(INR)的测量。根据常规临床实践调整治疗。使用非线性混合效应模型进行数据分析,并使用 MONOLIX 3.2 估计参数。fluindione 的药代动力学(PK)为单室模型,而 INR 的演变则根据周转率模型(维生素 K 再循环的抑制)进行建模。个体间变异性(IIV)非常大。清除率随年龄和 cordarone 的先前给药而降低。在研究之前接受过手术的患者的 IC50 值较低,导致对 fluindione 的敏感性增加。老年患者的药代动力学暴露显著增加,需要降低 fluindione 的剂量。