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Children in clinical trials: survey on the current situation in paediatric university clinics in Germany

机译:儿童正在接受临床试验:德国儿科大学诊所的现状调查

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Many prescribed treatments for children have not been adequately tested in children, sometimes resulting in harmful treatments being given and beneficial treatments being withheld. In the absence of specific trial-based data in children, results of studies in adults are extrapolated, which is often inappropriate because children have different range of diseases and metabolize medications differently. Trials in children are more challenging than those in adults and the pool of eligible children entering trials is often small. Children must have at last the same rights as adults in relation to receiving treatment with medicinal products that have been fully tested. The need for more studies to obtain paediatric information for medicines used in children is now a matter of consensus on a global basis and is considered a public health priority. Therfore a survey was performed in university hospitals in Germany targeting the current and future situation of children in clinical trials. The questionnaire of this survey was sent to 68 paediatric departments in 31 university clinics in Germany with a respond rate of 27% with respect to 18 returned questionnaires. With regard to new laws, guidelines and strong governmental support and funding an increasing number of clinical trials is expected. Surprisingly, the number of trials in the paediatric population remains unchanged within a period of 4 years (2005-2008). Added to the surveys performed within the pharmaceutical industry from Heinrich and Hark the number of trials in children remains unchanged even within a period of 9 years (2000-2008). The efforts undertaken by the government regarding funding and supporting KKS (Coordinating Centers for Clinical Trials) and affiliated PAED-Net (Pediatric Network on Medication Development and Testing in Children and Adolescents at KKS) appear to be insufficient. Beginning of this year the legal framework with the urgent expected “Paediatric Regulation” was established. May be the implementation by clinicians and pharmaceutical industry will improve the current situation.
机译:许多针对儿童的处方治疗尚未在儿童中得到充分测试,有时会导致使用有害的治疗方法,并放弃有益的治疗方法。在没有针对儿童的特定基于试验的数据的情况下,对成人的研究结果进行推论,这通常是不合适的,因为儿童的疾病范围不同且药物的代谢方式也不同。儿童试验比成人试验更具挑战性,参加试验的合格儿童人数通常很少。在接受经过充分测试的药物治疗方面,儿童最终必须具有与成年人相同的权利。现在需要对更多的研究来获得儿童使用的药物的儿科信息已经成为全球共识,被认为是公共卫生的优先事项。因此,在德国的大学医院进行了一项针对儿童临床试验当前和未来状况的调查。该调查问卷已发送到德国31个大学诊所的68个儿科部门,对18份返回的问卷的答复率为27%。关于新法律,指南以及政府的大力支持和资助,预计将有越来越多的临床试验。令人惊讶的是,在4年(2005-2008年)内,儿科人群的试验次数保持不变。除Heinrich和Hark在制药行业进行的调查外,即使在9年内(2000-2008年),针对儿童的试验次数也保持不变。政府在资助和支持KKS(临床试验协调中心)和附属的PAED-Net(KKS儿童和青少年药物开发和测试的儿科网络)方面所做的努力似乎不足。从今年年初开始,建立了带有迫切期望的“儿科法规”的法律框架。由临床医生和制药业实施可能会改善目前的状况。

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