Drug dosage individualization based on a random-effects linear model.
نویسندگان
چکیده
This article investigates drug dosage individualization when the patient population can be described with a random-effects linear model of a continuous pharmacokinetic or pharmacodynamic response. Specifically, we show through both decision-theoretic arguments and simulations that a published clinical algorithm may produce better individualized dosages than some traditional methods of therapeutic drug monitoring. Since empirical evidence suggests that the linear model may adequately describe drugs and patient populations, and linear models are easier to handle than the nonlinear models traditionally used in population pharmacokinetics, our results highlight the potential applicability of linear mixed models to dosage computations and personalized medicine.
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Center). The contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH.
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عنوان ژورنال:
- Journal of biopharmaceutical statistics
دوره 22 3 شماره
صفحات -
تاریخ انتشار 2012