Holford Nick H G, Anderson Brian J
Department of Pharmacology & Clinical Pharmacology, University of Auckland, New Zealand.
Department of Anaesthesiology, University of Auckland, New Zealand.
Br J Clin Pharmacol. 2017 Apr;83(4):685-687. doi: 10.1111/bcp.13230. Epub 2017 Feb 2.
Germovsek and colleagues have recently concluded that a standard approach to modelling pharmacokinetics is not wrong and appears to be at least as useful as other ad hoc methods for describing drug concentrations. There are other advantages of this approach including learning about biology, comparing different studies, detecting errors and rationalizing dose prediction. A standard approach to size and maturation is not a panacea but provides the framework for challenging new ideas and supports a consistent method of dosing in patients of all ages.
格莫夫塞克及其同事最近得出结论,标准的药代动力学建模方法并无错误,而且似乎至少与其他用于描述药物浓度的临时方法一样有用。这种方法还有其他优点,包括了解生物学知识、比较不同研究、检测误差以及使剂量预测合理化。标准的体型和成熟度方法并非万灵药,但它为挑战新观点提供了框架,并支持在所有年龄段患者中采用一致的给药方法。