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安全且有效的可变性——剂量个体化的标准。

Safe and effective variability-a criterion for dose individualization.

机构信息

Department of Pharmacology & Clinical Pharmacology, University of Auckland, Auckland, New Zealand.

出版信息

Ther Drug Monit. 2012 Oct;34(5):565-8. doi: 10.1097/FTD.0b013e31826aabc3.

Abstract

BACKGROUND

A primary goal of clinical pharmacology is to understand the factors that determine the dose-effect relationship and to use this knowledge to individualize drug dose.

METHODS

A principle-based criterion is proposed for deciding among alternative individualization methods.

RESULTS

Safe and effective variability defines the maximum acceptable population variability in drug concentration around the population average.

CONCLUSIONS

A decision on whether patient covariates alone are sufficient, or whether therapeutic drug monitoring in combination with target concentration intervention is needed, can be made by comparing the remaining population variability after a particular dosing method with the safe and effective variability.

摘要

背景

临床药理学的主要目标之一是了解决定剂量-效应关系的因素,并利用这一知识实现药物剂量个体化。

方法

提出了一种基于原理的标准,用于在替代个体化方法之间做出决策。

结果

安全有效的可变性定义了药物浓度围绕人群平均值的最大可接受个体间变异性。

结论

通过比较特定给药方法后剩余的群体变异性与安全有效的变异性,可以确定仅患者协变量是否足够,或者是否需要结合治疗药物监测和目标浓度干预。

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