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日本儿童新型抗生素的临床试验。

Clinical trials of new antibiotics in children in Japan.

作者信息

Fujii R

机构信息

Institute of Chemotherapy for Mother and Child, Tokyo, Japan.

出版信息

Acta Paediatr Jpn. 1997 Feb;39(1):98-104. doi: 10.1111/j.1442-200x.1997.tb03566.x.

Abstract

Japan is the most advanced of the industrialized nations in the development of antibiotics. Compared to the United States and countries of the European Union, there is a rich selection and availability of new and appropriate antibiotics for patients with infectious diseases in Japan that is unchallenged under a medical system where its people are all covered by a national health insurance plan. This can also be said in the area of antimicrobial treatment of children and newborns. In Japan, the turning point (T-point), which the author defines as the point when the average life expectancy of newborns equals that of 1 year olds, was in 1970. Keeping infant deaths from infectious diseases under control was indispensable for this achievement, to which antibiotics had greatly contributed. After the T-point, another methodology was needed in pediatrics. The situation in Japan, where most newly developed antibiotics are equipped with statements concerning methods of administration, dosage and safety for children or newborns, differs considerably from overseas situation. The procedures and methods of the clinical trials on children that were performed in strict compliance with good clinical practice are described. Trial studies cannot be performed easily in Japan. Next, the reason why the clinical trials of the antibiotics in pediatrics were performed and accurately evaluated without incident over 50 years by comparatively small numbers of specialists and facilities is described historically and retrospectively. During the 30 years since modern methods were established, clinical trials of antibiotics with children and newborns have been performed only on essential agents; about one-half and one-third, respectively, of the 91 new antibiotics on which clinical trials with adults were conducted. The author has recently published evaluation criteria for clinical studies on antibiotics in the pediatric field. In addition, as the trial's director/administrator, the author states his concept for future clinical development of new antibiotics for children.

摘要

在抗生素研发方面,日本是工业化国家中最先进的。与美国和欧盟国家相比,在全民纳入国民健康保险计划的医疗体系下,日本为传染病患者提供了丰富多样且合适的新型抗生素,这一点无可比拟。在儿童和新生儿抗菌治疗领域也是如此。作者将新生儿平均预期寿命与1岁幼儿相等的那个点定义为转折点(T点),日本的转折点出现在1970年。控制婴儿因传染病导致的死亡对于这一成就不可或缺,抗生素对此贡献巨大。在转折点之后,儿科需要另一种方法。日本的情况与海外不同,大多数新研发的抗生素都配有关于儿童或新生儿给药方法、剂量和安全性的说明。描述了严格按照良好临床实践进行的儿童临床试验的程序和方法。在日本进行试验研究并非易事。接下来,从历史和回顾的角度描述了为何儿科抗生素临床试验能在50多年间由相对较少的专家和机构顺利进行并得到准确评估。自现代方法确立后的30年里,仅对必需药物进行了儿童和新生儿抗生素临床试验;在针对成人进行临床试验的91种新型抗生素中,儿童和新生儿临床试验分别约占一半和三分之一。作者最近发表了儿科领域抗生素临床研究的评估标准。此外,作为试验的主任/管理者,作者阐述了他对未来儿童新型抗生素临床开发的理念。

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