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产品特性摘要中信息对肾功能损害患者剂量调整的临床意义。

Clinical relevance of information in the Summaries of Product Characteristics for dose adjustment in renal impairment.

机构信息

Research Institute for Medicines and Pharmaceutical Sciences (iMed.UL), Faculty of Pharmacy, University of Lisbon, Av. Prof. Gama Pinto, 1649-003, Lisbon, Portugal.

出版信息

Eur J Clin Pharmacol. 2013 Nov;69(11):1973-9. doi: 10.1007/s00228-013-1560-2. Epub 2013 Jul 25.

Abstract

PURPOSE

Information about dosing adjustments in patients with chronic kidney disease is important to avoid toxicity for several medicines. The aim of our study was to assess the clinical relevance of the instructions for dose adjustment in patients with renal impairment provided in the Summaries of Product Characteristics (SmPCs) approved by the European Medicines Agency (EMA).

METHODS

SmPCs available on the EMA website on April 2011 were retrieved, and information on the elimination route and instructions for use in renal impairment was analysed independently by two of the authors. SmPCs were classified as containing 'explicit' or 'poor' information based on whether they presented (or not) instructions for use of the medicine in renal impairment. Information was considered 'relevant' if SmPCs provided clear instructions for dose adjustment.

RESULTS

Of the 356 SmPCs analysed, 13.8 and 37.4 % were classified as providing poor information and explicit but not relevant information, respectively. Only 48.8 % SmPCs provided both explicit and relevant information on medicine use in renal impairment. No difference was found in the average time since last update among SmPCs classified as containing explicit or poor information, as well as those classified as containing relevant or not relevant information. Also, no association was found between the clinical relevance of the information and whether or not the medication was an orphan drug, and 80 % SmPCs did not provide information on the use of the medicine in patients undergoing haemodialysis.

CONCLUSIONS

Based on our analysis, current versions of SmPCs are characterised by several information deficits and by containing recommendations that are not relevant to clinical practice in terms of dose adjustment in renal impairment. These shortcomings might limit their usefulness for healthcare professionals and integration into clinical decision-making support systems.

摘要

目的

对于多种药物,了解慢性肾脏病患者的剂量调整信息对于避免毒性非常重要。我们的研究旨在评估欧洲药品管理局(EMA)批准的产品特性摘要(SmPC)中针对肾功能损害患者的剂量调整说明的临床相关性。

方法

检索了 EMA 网站上 2011 年 4 月的 SmPC,由两位作者独立分析有关消除途径和肾功能损害使用说明的信息。根据是否提供肾功能损害时药物使用说明,将 SmPC 分为“明确”或“差”信息。如果 SmPC 提供了明确的剂量调整说明,则认为信息是“相关”的。

结果

在分析的 356 份 SmPC 中,分别有 13.8%和 37.4%被归类为提供差信息和明确但不相关信息。只有 48.8%的 SmPC 提供了肾功能损害时药物使用的明确和相关信息。分类为明确或差信息的 SmPC 之间,以及分类为相关或不相关信息的 SmPC 之间,自上次更新以来的平均时间没有差异。此外,信息的临床相关性与药物是否为孤儿药之间也没有关联,80%的 SmPC 未提供血液透析患者使用药物的信息。

结论

根据我们的分析,当前版本的 SmPC 存在几个信息缺陷,并且包含的剂量调整建议与肾功能损害的临床实践无关。这些缺陷可能会限制它们对医疗保健专业人员的有用性,并限制它们整合到临床决策支持系统中。

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