Drug-induced cardiac toxicity and adverse drug reactions, a narrative review

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY Therapie Pub Date : 2024-03-01 DOI:10.1016/j.therap.2023.10.008
Alexandre Destere , Diane Merino , Thibaud Lavrut , Fanny Rocher , Delphine Viard , Milou-Daniel Drici , Alexandre O. Gérard
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Abstract

Drug-induced cardiotoxicity is a primary concern in both drug development and clinical practice. Although the heart is not a common target for adverse drug reactions, some drugs still cause various adverse cardiac events, with sometimes severe consequences. Direct cardiac toxicity encompasses functional and structural changes of the cardiovascular system due to possible exposure to medicines. This phenomenon extends beyond cardiovascular drugs to include non-cardiovascular drugs including anticancer drugs such as tyrosine kinase inhibitors, anthracyclines and immune checkpoint inhibitors (ICIs), as well as various antipsychotics, venlafaxine, and even some antibiotics (such as macrolides). Cardiac ADRs comprise an array of effects, ranging from heart failure and myocardial ischemia to valvular disease, thrombosis, myocarditis, pericarditis, arrhythmias, and conduction abnormalities. The underlying mechanisms may include disturbances of ionic processes, induction of cellular damage via impaired mitochondrial function, and even hypercoagulability. To mitigate the impact of drug-induced cardiotoxicity, multi-stage evaluation guidelines have been established, following the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines for in vitro and in vivo testing. Despite preclinical safeguards, post-marketing surveillance remains critical, as certain cardiotoxic drugs may escape initial scrutiny. Indeed, historical data show that cardiovascular ADRs contribute to almost 10% of market withdrawals. The impact of drug-induced cardiotoxicity on cardiac issues, particularly heart failure, is often underestimated, with incidence rates ranging from 11.0% to over 20.0%. We here comprehensively examine different patterns of drug-induced cardiotoxicity, highlighting current concerns and emerging pharmacovigilance signals. Understanding the underlying mechanisms and the associated risk factors is critical in order to promptly identify, effectively manage, and proactively prevent drug-induced cardiac adverse events. Collaborative efforts between physicians and cardiologists, coupled with thorough assessment and close monitoring, are essential to ensuring patient safety in the face of potential drug-induced cardiotoxicity.

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药物引起的心脏毒性和药物不良反应的叙述综述。
药物引起的心脏毒性是药物开发和临床实践中主要关注的问题。虽然心脏不是药物不良反应的常见目标,但一些药物仍然会引起各种不良的心脏事件,有时会产生严重的后果。直接心脏毒性包括由于可能暴露于药物而引起的心血管系统功能和结构变化。这一现象不仅限于心血管类药物,还包括非心血管类药物,如酪氨酸激酶抑制剂、蒽环类药物和免疫检查点抑制剂(ICIs)等抗癌药物,以及各种抗精神病药物、文拉法辛,甚至一些抗生素(如大环内酯类药物)。心脏不良反应包括一系列影响,从心力衰竭和心肌缺血到瓣膜疾病、血栓形成、心肌炎、心包炎、心律失常和传导异常。潜在的机制可能包括离子过程的干扰,通过线粒体功能受损诱导细胞损伤,甚至高凝性。为了减轻药物引起的心脏毒性的影响,根据国际人用药品技术要求协调委员会(ICH)体外和体内试验指南,已经建立了多阶段评估指南。尽管有临床前的保障措施,但上市后的监督仍然至关重要,因为某些心脏毒性药物可能会逃避最初的审查。事实上,历史数据显示,心血管不良反应占市场退出的近10%。药物引起的心脏毒性对心脏问题,特别是心力衰竭的影响往往被低估,其发生率从11.0%到20.0%以上。我们在这里全面检查不同模式的药物引起的心脏毒性,突出当前的关注和新出现的药物警戒信号。了解潜在的机制和相关的危险因素对于及时识别、有效管理和主动预防药物性心脏不良事件至关重要。医生和心脏病专家之间的合作努力,加上彻底的评估和密切的监测,对于面对潜在的药物引起的心脏毒性,确保患者的安全至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapie
Therapie 医学-药学
CiteScore
3.50
自引率
7.70%
发文量
132
审稿时长
57 days
期刊介绍: Thérapie is a peer-reviewed journal devoted to Clinical Pharmacology, Therapeutics, Pharmacokinetics, Pharmacovigilance, Addictovigilance, Social Pharmacology, Pharmacoepidemiology, Pharmacoeconomics and Evidence-Based-Medicine. Thérapie publishes in French or in English original articles, general reviews, letters to the editor reporting original findings, correspondence relating to articles or letters published in the Journal, short articles, editorials on up-to-date topics, Pharmacovigilance or Addictovigilance reports that follow the French "guidelines" concerning good practice in pharmacovigilance publications. The journal also publishes thematic issues on topical subject. The journal is indexed in the main international data bases and notably in: Biosis Previews/Biological Abstracts, Embase/Excerpta Medica, Medline/Index Medicus, Science Citation Index.
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