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2007 年发表的儿科随机对照药物试验的系统评价。

A systematic review of paediatric randomised controlled drug trials published in 2007.

机构信息

Academic Division of Child Health, School of Graduate Entry Medicine and Health Sciences, University of Nottingham, Derby, UK.

出版信息

Arch Dis Child. 2010 Jun;95(6):469-73. doi: 10.1136/adc.2009.173591.

Abstract

OBJECTIVE

To elucidate the current situation of randomised drug trials involving the paediatric population.

METHODS

Systematic review of paediatric randomised controlled trials of medicinal products published in 2007. Three major databases were searched with validated search strategies; Medline, Embase and Cochrane Central Register of Controlled Clinical Trials. Data was collected on the location, participants, class of drug and methodological quality of the trials.

RESULTS

Six hundred and four trials were found involving more than 100,000 paediatric participants. Only about a quarter (146, 24%) were conducted in low and lower-middle income countries. Few studies (42, 7%) were performed in neonates. Many trials recruiting both adult and paediatric patients inadequately describe the characteristics of the paediatric participants. The most studied areas were nervous system (155, 26%), anti-infective (101, 17%) respiratory (74, 12%) or antiparasitic (45, 8%) drugs. A high proportion of the studies (36%) used an inactive placebo as the comparator. Paediatric randomised drug trials performed in low and low-middle income countries were of lower methodological quality (mean Jadad score 2.90 vs 3.27, p<0.01), studied more antiparasitic and anti-infectives (47% vs 16%, p<0.01) but fewer reported that ethical approval was obtained (83% vs 93%, p<0.01), compared to those conducted in high or upper-middle income countries.

CONCLUSIONS

There are a significant number of randomised controlled drug trials involving children taking place throughout the world. To develop the evidence base for safe and effective medicines for the benefit of the whole paediatric population, high quality and ethical clinical trials should involve a wide range of children.

摘要

目的

阐明涉及儿科人群的随机药物试验的现状。

方法

对 2007 年发表的儿科随机对照药物试验进行系统评价。使用经过验证的搜索策略在三个主要数据库中进行搜索:Medline、Embase 和 Cochrane 对照临床试验中心注册库。收集试验的地点、参与者、药物类别和方法学质量的数据。

结果

共发现 604 项涉及超过 10 万名儿科参与者的试验。只有约四分之一(146 项,24%)在低收入和中下收入国家进行。很少有研究(42 项,7%)在新生儿中进行。许多招募成人和儿科患者的试验未能充分描述儿科参与者的特征。研究最多的领域是神经系统(155 项,26%)、抗感染(101 项,17%)、呼吸(74 项,12%)或抗寄生虫(45 项,8%)药物。相当一部分研究(36%)使用非活性安慰剂作为对照。在低收入和中下收入国家进行的儿科随机药物试验方法学质量较低(平均 Jadad 评分 2.90 与 3.27,p<0.01),研究更多的抗寄生虫和抗感染药物(47%与 16%,p<0.01),但报告获得伦理批准的比例较低(83%与 93%,p<0.01)与在高收入或中上收入国家进行的试验相比。

结论

全世界范围内有大量涉及儿童的随机对照药物试验。为了为整个儿科人群的安全有效药物的发展提供证据基础,高质量和符合伦理的临床试验应包括广泛的儿童。

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