{"title":"Pediatric Myocarditis: Challenges in Diagnosis and Treatment.","authors":"Bibhuti B Das","doi":"10.1007/s40272-026-00739-4","DOIUrl":null,"url":null,"abstract":"<p><p>Pediatric myocarditis is a clinically diverse and often under-recognized inflammatory condition of the myocardium, with presentations that range from mild symptoms to acute heart failure. Advances in cardiac imaging, biomarker discovery, and molecular genetics have improved diagnostic precision and individualized care. Genetic studies indicate that 8-10% of pediatric patients with myocarditis carry pathogenic variants in cardiomyopathy-related genes, supporting the \"double-hit\" hypothesis where genetic predisposition interacts with viral or autoimmune triggers. This paradigm shift has underscored the relevance of precision medicine, emphasizing tailored management based on the underlying etiology and genetic background. While supportive care remains the foundation of therapy, including rest, hemodynamic monitoring, and guideline-directed medical therapy for heart failure, pharmacologic strategies are evolving. Corticosteroids are under investigation for modulating inflammation, with mixed results showing improvements in ventricular function but unclear survival benefits. Immunomodulatory agents, such as intravenous immunoglobulin and other immunosuppressive therapies, offer promise in reducing myocardial fibrosis and injury. Virus-specific therapies are increasingly utilized in confirmed viral myocarditis, improving outcomes in selected cases. Recent studies highlight the potential role of biologic agents targeting inflammatory pathways, such as interferons, interleukin modulators, and micro-RNA-based therapy in refractory cases. Despite limited pediatric-specific trial data, extrapolation from adult myocarditis studies continues to inform treatment direction. Continued translational research and pediatric-focused clinical trials are critical to optimizing treatment of myocarditis and improving long-term cardiac outcomes. Future investigations should focus on refining immunomodulatory strategies, identifying novel therapeutic targets, and enhancing risk stratification to improve individualized care.</p>","PeriodicalId":19955,"journal":{"name":"Pediatric Drugs","volume":" ","pages":"249-268"},"PeriodicalIF":3.3000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Drugs","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s40272-026-00739-4","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/7 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0
Abstract
Pediatric myocarditis is a clinically diverse and often under-recognized inflammatory condition of the myocardium, with presentations that range from mild symptoms to acute heart failure. Advances in cardiac imaging, biomarker discovery, and molecular genetics have improved diagnostic precision and individualized care. Genetic studies indicate that 8-10% of pediatric patients with myocarditis carry pathogenic variants in cardiomyopathy-related genes, supporting the "double-hit" hypothesis where genetic predisposition interacts with viral or autoimmune triggers. This paradigm shift has underscored the relevance of precision medicine, emphasizing tailored management based on the underlying etiology and genetic background. While supportive care remains the foundation of therapy, including rest, hemodynamic monitoring, and guideline-directed medical therapy for heart failure, pharmacologic strategies are evolving. Corticosteroids are under investigation for modulating inflammation, with mixed results showing improvements in ventricular function but unclear survival benefits. Immunomodulatory agents, such as intravenous immunoglobulin and other immunosuppressive therapies, offer promise in reducing myocardial fibrosis and injury. Virus-specific therapies are increasingly utilized in confirmed viral myocarditis, improving outcomes in selected cases. Recent studies highlight the potential role of biologic agents targeting inflammatory pathways, such as interferons, interleukin modulators, and micro-RNA-based therapy in refractory cases. Despite limited pediatric-specific trial data, extrapolation from adult myocarditis studies continues to inform treatment direction. Continued translational research and pediatric-focused clinical trials are critical to optimizing treatment of myocarditis and improving long-term cardiac outcomes. Future investigations should focus on refining immunomodulatory strategies, identifying novel therapeutic targets, and enhancing risk stratification to improve individualized care.
期刊介绍:
Pediatric Drugs promotes the optimization and advancement of all aspects of pharmacotherapy for healthcare professionals interested in pediatric drug therapy (including vaccines). The program of review and original research articles provides healthcare decision makers with clinically applicable knowledge on issues relevant to drug therapy in all areas of neonatology and the care of children and adolescents. The Journal includes:
-overviews of contentious or emerging issues.
-comprehensive narrative reviews of topics relating to the effective and safe management of drug therapy through all stages of pediatric development.
-practical reviews covering optimum drug management of specific clinical situations.
-systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement.
-Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in the pediatric population.
-original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies.
Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Pediatric Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.