Batchelor Hannah K, Marriott John F
Br J Clin Pharmacol. 2015 Mar;79(3):405-18. doi: 10.1111/bcp.12268.
Paediatric formulation design is complex as there is a need to understand the developmental physiological changes that occur during childhood and their impact on the absorption of drugs. Paediatric dose adjustments are usually based on achieving pharmacokinetic or pharmacodynamic profiles equivalent to those achieved in adult populations. However, differences in the way in which children handle adult products or the use of bespoke paediatric formulations can result in unexpected pharmacokinetic drug profiles with altered clinical efficacy. Differences in drug formulations need to be understood by healthcare professionals involved in the prescribing, administration or dispensing of drugs to children such that appropriate advice is given to ensure that therapeutic outcomes are achieved. This issue is not confined to oral medicines but is applicable for all routes of administration encountered in paediatric therapy.
儿科制剂设计很复杂,因为需要了解儿童时期发生的发育生理变化及其对药物吸收的影响。儿科剂量调整通常基于实现与成人人群相当的药代动力学或药效学特征。然而,儿童使用成人产品的方式差异或定制儿科制剂的使用可能导致意外的药代动力学药物特征,临床疗效改变。参与给儿童开药、给药或配药的医疗保健专业人员需要了解药物制剂的差异,以便提供适当建议,确保实现治疗效果。这个问题不仅限于口服药物,也适用于儿科治疗中遇到的所有给药途径。