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原发性线粒体疾病患者药物使用的安全性:基于国际德尔菲共识的研究。

Safety of drug use in patients with a primary mitochondrial disease: An international Delphi-based consensus.

机构信息

Radboudumc Amalia Children's Hospital, Radboud Center for Mitochondrial Medicine, Nijmegen, The Netherlands.

Department of Human Nutrition, Foods, and Exercise and the Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia.

出版信息

J Inherit Metab Dis. 2020 Jul;43(4):800-818. doi: 10.1002/jimd.12196. Epub 2020 Feb 7.

Abstract

Clinical guidance is often sought when prescribing drugs for patients with primary mitochondrial disease. Theoretical considerations concerning drug safety in patients with mitochondrial disease may lead to unnecessary withholding of a drug in a situation of clinical need. The aim of this study was to develop consensus on safe medication use in patients with a primary mitochondrial disease. A panel of 16 experts in mitochondrial medicine, pharmacology, and basic science from six different countries was established. A modified Delphi technique was used to allow the panellists to consider draft recommendations anonymously in two Delphi rounds with predetermined levels of agreement. This process was supported by a review of the available literature and a consensus conference that included the panellists and representatives of patient advocacy groups. A high level of consensus was reached regarding the safety of all 46 reviewed drugs, with the knowledge that the risk of adverse events is influenced both by individual patient risk factors and choice of drug or drug class. This paper details the consensus guidelines of an expert panel and provides an important update of previously established guidelines in safe medication use in patients with primary mitochondrial disease. Specific drugs, drug groups, and clinical or genetic conditions are described separately as they require special attention. It is important to emphasise that consensus-based information is useful to provide guidance, but that decisions related to drug prescribing should always be tailored to the specific needs and risks of each individual patient. We aim to present what is current knowledge and plan to update this regularly both to include new drugs and to review those currently included.

摘要

当为原发性线粒体疾病患者开处方时,通常会寻求临床指导。关于线粒体疾病患者药物安全性的理论考虑可能导致在临床需要的情况下不必要地拒绝使用药物。本研究的目的是就原发性线粒体疾病患者安全用药达成共识。成立了一个由来自六个不同国家的线粒体医学、药理学和基础科学领域的 16 名专家组成的专家组。使用改良 Delphi 技术允许小组成员在两轮 Delphi 中匿名考虑草案建议,两轮 Delphi 具有预定的共识水平。该过程得到了对现有文献的审查和包括小组成员和患者权益团体代表在内的共识会议的支持。专家组就所有 46 种已审查药物的安全性达成了高度共识,他们认识到不良事件的风险既受个体患者风险因素的影响,也受药物或药物类别选择的影响。本文详细介绍了专家组的共识指南,并提供了对以前在原发性线粒体疾病患者安全用药方面建立的指南的重要更新。具体药物、药物组和临床或遗传条件分别进行了描述,因为它们需要特别注意。重要的是要强调,基于共识的信息有助于提供指导,但与药物处方相关的决策应始终根据每个患者的具体需求和风险进行调整。我们旨在介绍当前的知识,并计划定期更新,以包括新的药物,并审查目前包括的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1494/7383489/b3f98251fc63/JIMD-43-800-g001.jpg

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