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日本儿科超说明书使用成人适应证精神药品情况调查:基于美国儿科患者药品审批信息的研究

Pediatric off-label use of psychotropic drugs approved for adult use in Japan in the light of approval information regarding pediatric patients in the United States: a study of a pharmacy prescription database.

机构信息

Division of Drug Development and Regulatory Science, Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.

Department of Child Psychiatry, Chiba University Hospital, Chiba, Japan.

出版信息

World J Pediatr. 2019 Feb;15(1):92-99. doi: 10.1007/s12519-018-0213-z. Epub 2018 Nov 30.

Abstract

BACKGROUND

Off-label use of psychotropic prescriptions for pediatric patients has been increasing in Japan. This study sought to clarify pediatric patients' off-label use of psychotropics approved only for adults in Japan.

METHODS

This retrospective study on psychotropic utilization employed a pharmaceutical health insurance claims database supplied by a pharmacy for the fiscal year 2016. Seven psychotropic drugs were examined. For each drug, we calculated the proportion of patients aged < 16 years or who were under the approved age limit set in the United States out of all patients. The maximum daily dose of each drug within the study period was plotted by age.

RESULTS

Data of 45,715 patients (female: 26,799, male: 18,916) with 331,920 prescriptions were examined in this study. For each drug, the proportion of pediatric patients aged < 16 years ranged from 0.15 to 1.1%, while the proportion of those under the approved age limit in the United States ranged from 0 to 0.27%. Olanzapine had the highest reported proportion. No drugs other than olanzapine were taken under the approved age limit in the United States.

CONCLUSIONS

We identified the pediatric off-label use of psychotropics that were limited to adult use in Japan. The results indicated the possibility of referring to international guidelines or evidence in clinical practice, but these factors do not discount the existing problems with off-label use. More clinical trials within the pediatric population in Japan are needed to address the issue of off-label use and obtain useful and reliable information in the package inserts for rational use in future pediatric patients.

摘要

背景

在日本,精神科处方的标签外使用在儿科患者中呈上升趋势。本研究旨在阐明日本仅批准成人使用的精神药物在儿科患者中的标签外使用情况。

方法

本项关于精神药物使用的回顾性研究利用了一家药店提供的 2016 财年的药品健康保险索赔数据库。研究中检查了 7 种精神药物。对于每种药物,我们计算了所有患者中年龄<16 岁或低于美国批准年龄限制的患者比例。在研究期间,按年龄绘制了每种药物的最大日剂量。

结果

本研究共检查了 45715 名患者(女性 26799 名,男性 18916 名)的 331920 份处方。对于每种药物,年龄<16 岁的儿科患者比例从 0.15%到 1.1%不等,而低于美国批准年龄限制的患者比例从 0%到 0.27%不等。奥氮平的报告比例最高。除奥氮平外,没有其他药物在美国批准的年龄限制内使用。

结论

我们发现了日本限制成人使用的精神药物在儿科中的标签外使用。结果表明,在临床实践中可能需要参考国际指南或证据,但这些因素并不能忽视标签外使用现有的问题。日本需要在儿科人群中进行更多的临床试验,以解决标签外使用问题,并在未来儿科患者的合理使用中获得有用和可靠的信息。

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