Current Status of Pharmacokinetic Research in Children: A Systematic Review of Clinical Trial Records.

IF 1.3 Q4 PHARMACOLOGY & PHARMACY
Pugazhenthan Thangaraju, Hemasri Velmurugan, Krishnapriya Neelambaran
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Abstract

Background: Many medications have different pharmacokinetics in children than in adults. Knowledge about the safety and efficacy of medications in children requires research into the pharmacokinetic profiles of children's medicines. By analysing registered clinical trial records, this study determined how frequently pharmacokinetic data is gathered in paediatric drug trials.

Methods: We searched for the pharmacokinetic data from clinical trial records for preterm infants and children up to the age of 16 from January 2011 to April 2022. The records of trials involving one or more drugs in preterm infants and children up to the age of 16 were examined for evidence that pharmacokinetic data would be collected.

Results: In a total of 1483 records of interventional clinical trials, 136 (9.17%) pharmacokinetic data involved adults. Of those 136 records, 60 (44.1%) records were pharmacokinetics trials involving one or more medicines in children up to the age of 16.20 (33.3%) in America, followed by 19 (31.6%) in Europe. Most trials researched medicines in the field of infection or parasitic diseases 20 (33.3%). 27 (48.2%) and 26 (46.4%) trials investigated medicines that were indicated as essential medicine.

Conclusion: The pharmacokinetic characteristics of children's drugs need to be better understood. The current state of pharmacokinetic research appears to address the knowledge gap in this area adequately. Despite slow progress, paediatric clinical trials have experienced a renaissance as the significance of paediatric trials has gained international attention. The outcome of paediatric trials will have an impact on children's health in the future. In recent years, the need for greater availability and access to safe child-size pharmaceuticals has received a lot of attention.

儿童药代动力学研究现状:临床试验记录的系统回顾。
背景:许多药物在儿童体内的药代动力学与成人不同。要了解儿童用药的安全性和有效性,就必须研究儿童药物的药代动力学特征。本研究通过分析已登记的临床试验记录,确定在儿科药物试验中收集药代动力学数据的频率:我们搜索了 2011 年 1 月至 2022 年 4 月期间早产儿和 16 岁以下儿童临床试验记录中的药代动力学数据。我们对涉及早产儿和 16 岁以下儿童的一种或多种药物的试验记录进行了检查,以确定是否有证据表明收集了药代动力学数据:在总共 1483 份介入性临床试验记录中,有 136 份(9.17%)涉及成人的药代动力学数据。在这 136 条记录中,有 60 条(44.1%)是涉及 16 岁以下儿童的一种或多种药物的药代动力学试验,其中 20 条(33.3%)在美国,其次是 19 条(31.6%)在欧洲。大多数试验研究的是感染或寄生虫病领域的药物 20 项(33.3%)。有 27 项(48.2%)和 26 项(46.4%)试验研究的药物被列为基本药物:结论:需要更好地了解儿童药物的药代动力学特征。药代动力学研究的现状似乎足以弥补这方面的知识差距。尽管进展缓慢,但随着儿科临床试验的重要性得到国际关注,儿科临床试验已经历了一次复兴。儿科试验的结果将对未来儿童的健康产生影响。近年来,提供更多安全儿童规格药品的需求受到广泛关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
9.10%
发文量
55
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