Decompensated heart failure after one year of successful therapy with mavacamten: a case report.

IF 0.7 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
European Heart Journal: Case Reports Pub Date : 2026-10-07 eCollection Date: 2026-10-01 DOI:10.1093/ehjcr/ytag741
Giulia Marchionni, Lucrezia Netti, Silvia Stavagna, Cristina Chimenti
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引用次数: 0

Abstract

Background: Cardiac myosin inhibition is the first disease-specific therapeutic strategy for obstructive hypertrophic cardiomyopathy. Mavacamten, the first-in-class agent, has demonstrated an excellent safety profile and sustained efficacy in both clinical trials and real-world practice. However, its safe use requires careful monitoring and thorough patient education regarding potential drug-drug interactions.

Case summary: We report a case of acute heart failure occurring after long-term clinical stability on mavacamten following concomitant fluconazole administration. It is reasonable to assume that the pharmacokinetic interaction resulted in excessive mavacamten exposure, leading to transient systolic dysfunction, severe functional mitral regurgitation, and adverse left ventricular remodelling.

Discussion: This case report highlights the consequences of pharmacological interactions between mavacamten and a strong CYP2C19 inhibitor. Drug-drug interaction should always be considered and systematically excluded in a patient presenting with unexplained heart failure and left ventricular remodelling during mavacamten therapy.

马伐卡坦成功治疗一年后失代偿性心力衰竭1例报告。
背景:心肌肌球蛋白抑制是阻塞性肥厚性心肌病的第一种疾病特异性治疗策略。Mavacamten在临床试验和实际应用中均表现出良好的安全性和持续的疗效。然而,它的安全使用需要仔细监测和彻底的患者教育关于潜在的药物-药物相互作用。病例总结:我们报告了一例急性心力衰竭发生后,长期临床稳定的马伐卡坦与氟康唑联合用药。我们有理由认为,药代动力学相互作用导致过量的马伐卡坦暴露,导致短暂性收缩功能障碍、严重的功能性二尖瓣反流和不良的左心室重构。讨论:本病例报告强调了马伐卡坦与强CYP2C19抑制剂之间药理相互作用的后果。在马伐卡坦治疗期间出现原因不明的心力衰竭和左心室重构的患者,应始终考虑并系统地排除药物-药物相互作用。
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
European Heart Journal: Case Reports
European Heart Journal: Case Reports Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.30
自引率
10.00%
发文量
451
审稿时长
14 weeks
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