[儿童用药及推荐条件]。

Anales Espanoles De Pediatria Pub Date : 2002-11-01
I Danés Carreras, A Vallano Ferraz, G de la Cruz Sugrañes, J C Juárez Giménez, J M Arnau de Bolós
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引用次数: 0

摘要

背景:在其他国家进行的研究表明,在儿科人群药物调查、信息和授权稀缺的背景下,药物在批准条件之外用于儿童。目的:评价儿童推荐用药条件和药物信息来源的可变性。方法:我们进行了一项描述性、回顾性研究。1997年的药物消费数据来自一所儿科大学医院。使用西班牙药物目录分析儿童药物使用情况的信息。这一信息与北美目录的信息进行了比较,以供国际参考。结果:绝大多数使用的药物是无限制的(43;47%)或限制(26%;28%)儿童使用,但不推荐的药物(8;9%)或儿童中使用条件未明确的药物(15%;16%)。大约12%的药物未在北美目录中确定;其余药物中,60%为儿童无限制用药,35%为限制用药,5%为不推荐用药。结论:有相当比例的药物不推荐给住院儿童,或者这些药物在这一人群中可能的使用没有明确规定。值得鼓励研究,拥有有助于决策的信息来源,特别是在尚未获得批准的情况下,并使监管态度尽可能适应证据和治疗需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Drug utilization and recommended conditions for use in children].

Background: Studies carried out in other countries show that drugs are used in children outside the approved conditions, in a context in which investigation, information and authorization of medications in the pediatric population are scarce.

Objectives: To evaluate the conditions of drug use recommended in children and variability in sources of drug information.

Methods: We performed a descriptive, retrospective study. Data on medication consumption in 1997 were obtained from a pediatric university hospital. Information on conditions of drug use in children was analyzed using a Spanish catalog of medications. This information was compared with that of a North American catalog for international reference.

Results: Most of the drugs used were of unrestricted (43; 47 %) or restricted (26; 28 %) pediatric use, but drugs that are not recommended (8; 9 %) or those with unspecified conditions of use in children were also used (15; 16 %). Approximately 12 % of the drugs were not identified in the North American catalog; of the remaining drugs, 60 % were of unrestricted pediatric use, 35 % of restricted use and 5 % were not recommended.

Conclusions: A substantial proportion of drugs administered to hospitalized children are not recommended or their possible use in this population is not specified. It is worth encouraging research, having sources of information that help to make decisions, especially in conditions that have not been approved, and adapting regulatory attitudes, as far as possible, to the evidence and therapeutic needs.

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