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Paediatric pharmacokinetics: key considerations

机译:小儿药代动力学:主要考虑因素

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摘要

A number of anatomical and physiological factors determine the pharmacokinetic profile of a drug. Differences in physiology in paediatric populations compared with adults can influence the concentration of drug within the plasma or tissue. Healthcare professionals need to be aware of anatomical and physiological changes that affect pharmacokinetic profiles of drugs to understand consequences of dose adjustments in infants and children. Pharmacokinetic clinical trials in children are complicated owing to the limitations on blood sample volumes and perception of pain in children resulting from blood sampling. There are alternative sampling techniques that can minimize the invasive nature of such trials. Population based models can also limit the sampling required from each individual by increasing the overall sample size to generate robust pharmacokinetic data. This review details key considerations in the design and development of paediatric pharmacokinetic clinical trials.
机译:许多解剖和生理因素决定了药物的药代动力学特征。与成年人相比,儿科人群的生理差异可能会影响血浆或组织内药物的浓度。医疗保健专业人员需要了解影响药物药代动力学特征的解剖和生理变化,以了解婴儿和儿童剂量调整的后果。由于血液样本量的局限性以及对儿童因采血引起的疼痛感的限制,在儿童体内进行药代动力学临床试验非常复杂。有其他采样技术可以最大程度地减少此类试验的侵入性。基于人群的模型还可以通过增加总体样本量以生成可靠的药代动力学数据,来限制每个个体所需的样本。这篇综述详细介绍了儿科药代动力学临床试验设计和开发中的关键考虑因素。

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