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A factor VII-based method for the prediction of anticoagulant response to warfarin

机译:基于因子VII的方法预测华法林抗凝反应

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摘要

Warfarin dosing methods based on existing models for warfarin and the international normalised ratio (INR) give biased maintenance dose predictions at the upper and lower quantiles of dose requirements. The aim of this work is to propose a conceptually different approach to predict INR after warfarin dosing. Factor VII concentration was proposed as the principal driving force for the INR. The time to steady-state INR (tSS,INR) was determined based on the INR response to changes in factor VII concentrations following warfarin initiation, and from this the steady-state INR (INRSS) was derived. The proposed method requires timed, paired blood samples of INR and factor VII. At different simulated warfarin dose rates, the prediction error associated with the proposed method was shown to be within clinically acceptable limits for both the tSS,INR (±2 days) and INRSS (±0.2). The use of the method was demonstrated in two patients who were initiated with 5 mg of warfarin daily. The difference in predicted versus actual steady-state INR were 0.0 and −0.4. The proposed method represents a unique approach to predict the INR. It considers factor VII as the main driver for INR and provides valuable information about the time to steady state INR.
机译:基于现有华法林模型和国际标准化比率(INR)的华法林给药方法在较高和较低的剂量需求分位数下均得出有偏差的维持剂量预测。这项工作的目的是提出一种概念上不同的方法来预测华法林给药后的INR。建议将因子VII浓度作为INR的主要驱动力。根据华法令引发后对VII因子浓度变化的INR响应,确定达到稳态INR的时间(tSS,INR),并由此得出稳态INR(INRSS)​​。拟议的方法需要定时配对的INR和VII因子血样。在不同的模拟华法林剂量率下,与拟议方法相关的预测误差显示在tSS,INR(±2天)和INRSS(±0.2)的临床可接受范围内。在两名每天服用5微克华法林的患者中证明了该方法的使用。预测稳态INR与实际稳态INR之差为0.0和-0.4。所提出的方法代表了一种预测INR的独特方法。它认为因子VII是INR的主要驱动因素,并提供了有关达到INR稳态所需时间的宝贵信息。

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