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Variability and singularity arising from a Piecewise-Deterministic Markov Process applied to model poor patient compliance in the multi-Ⅳ case

机译:分段确定的Markov过程产生的变异性和奇点应用于模型患者符合多-∞案件的较差

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We propose a Piecewise-Deterministic Markov Process (PDMP) to model the drug concentration in the case of multiple intravenous-bolus (multi-IV) doses and poor patient adherence situation: the scheduled time and doses of drug administration are not respected by the patient, the drug administration considers switching regime with random drug intake times. We study the randomness of drug concentration and derive probability results on the stochastic dynamics using the PDMP theory, focusing on two aspects of practical relevance: the variability of the concentration and the regularity of its stationary probability distribution. The main result show as the regularity of the concentration is governed by a parameter, which quantifies in a precise way the situations where drug intake times are too scarce concerning the elimination rate. Our approach is novel for the study of the regularity of the stationary distribution in PDMP models. This article extends the results given in [J. Levy-Vehel and P.E. Levy-Vehel, Variability and singularity arising from poor compliance in a pharmacodynamical model I: The multi-IV case, J. Pharmacokinet. Pharmacodyn. 40 (2013), pp. 15-39], by considering more realistic irregular dosing schedules. The computations permit precise assessment of the effect of various significant parameters such as the mean rate of intake, the elimination rate, and the mean dose. They quantify how much poor adherence will affect the regimen. Our results help to understand the consequences of poor adherence.
机译:我们提出了一种分段确定的Markov方法(PDMP)来模拟在多个静脉内推注(多体IV)剂量和患者粘附情况的情况下的药物浓度:预定时间和药物管理剂量不受患者的尊重,药物管理局认为具有随机药物进气量的切换制度。我们研究药物浓度的随机性,并使用PDMP理论对随机动力学的概率产生概率,重点关注实际相关性的两个方面:浓度的变化和静止概率分布的规律性。主要结果表明作为浓度的规律性由参数控制,该参数以精确的方式量化药物进气量太少的情况而不是消除率。我们的方法是研究PDMP模型中固定分布规律性的新颖。本文扩展了[J. levy-veakel和p.e.征收载体,可变性和奇异性来自药效学模型的差,I:Multi-IV案例,J. Pharmacokinet。 Pharmacodyn。 40(2013),第15-39页],考虑更现实的不规则给药时间表。计算允许精确评估各种显着参数的效果,例如摄入量,消除率和平均剂量。它们量化了遵守较差的依从性会影响方案。我们的结果有助于了解粘附不良的后果。

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