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药物起效速率和作用持续时间如何影响药物宽恕。

How drug onset rate and duration of action affect drug forgiveness.

作者信息

Clark Elias D, Lawley Sean D

机构信息

Metrum Research Group, 2 Tunxis Road, Suite 112, Tariffville, CT, 06081, USA.

Department of Mathematics, University of Utah, Salt Lake City, UT, 84112, USA.

出版信息

J Pharmacokinet Pharmacodyn. 2024 Jun;51(3):213-226. doi: 10.1007/s10928-023-09897-1. Epub 2024 Jan 10.

Abstract

Medication nonadherence is one of the largest problems in healthcare today, particularly for patients undergoing long-term pharmacotherapy. To combat nonadherence, it is often recommended to prescribe so-called "forgiving" drugs, which maintain their effect despite lapses in patient adherence. Nevertheless, drug forgiveness is difficult to quantify and compare between different drugs. In this paper, we construct and analyze a stochastic pharmacokinetic/pharmacodynamic (PK/PD) model to quantify and understand drug forgiveness. The model parameterizes a medication merely by an effective rate of onset of effect when the medication is taken (on-rate) and an effective rate of loss of effect when a dose is missed (off-rate). Patient dosing is modeled by a stochastic process that allows for correlations in missed doses. We analyze this "on/off" model and derive explicit formulas that show how treatment efficacy depends on drug parameters and patient adherence. As a case study, we compare the effects of nonadherence on the efficacy of various antihypertensive medications. Our analysis shows how different drugs can have identical efficacies under perfect adherence, but vastly different efficacies for adherence patterns typical of actual patients. We further demonstrate that complex PK/PD models can indeed be parameterized in terms of effective on-rates and off-rates. Finally, we have created an online app to allow pharmacometricians to explore the implications of our model and analysis.

摘要

药物治疗不依从是当今医疗保健领域最大的问题之一,对于接受长期药物治疗的患者而言尤其如此。为了应对不依从问题,人们通常建议开所谓的“宽容性”药物,这类药物即便患者出现服药中断情况仍能保持疗效。然而,药物宽容性难以量化,也无法在不同药物之间进行比较。在本文中,我们构建并分析了一个随机药代动力学/药效学(PK/PD)模型,以量化并理解药物宽容性。该模型仅通过服药时效应的有效起效速率(开启速率)和漏服一剂时效应的有效丧失速率(关闭速率)来对药物进行参数化。患者给药情况通过一个随机过程进行建模,该过程考虑了漏服剂量之间的相关性。我们分析了这个“开启/关闭”模型,并推导出显式公式,展示了治疗效果如何取决于药物参数和患者依从性。作为一个案例研究,我们比较了不依从对各种抗高血压药物疗效的影响。我们的分析表明,不同药物在完美依从的情况下可能具有相同的疗效,但对于实际患者典型的依从模式,其疗效可能会有很大差异。我们进一步证明,复杂的PK/PD模型确实可以根据有效的开启速率和关闭速率进行参数化。最后,我们创建了一个在线应用程序,以便药理计量学家探索我们的模型和分析的意义。

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