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Parvovirus B19-associated fulminant acute myocarditis in children during the fifth disease outbreak in 2024: What
Mattia Pasquinucci1,2,3, Marco Scaglione1, Alessandra Siboldi4
1Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Insights
Pediatric myocarditis cases linked to Parvovirus B19 (PVB19) infections are rising post-COVID-19. This study of 5 children found severe heart dysfunction and variable outcomes with immunomodulatory therapy.
Area of Science:
- Pediatric Cardiology
- Viral Infections
- Immunology
Background:
- Myocarditis is a serious heart condition in children, often caused by viral infections.
- Parvovirus B19 (PVB19) is a key culprit, with recent reports indicating increased incidence post-COVID-19.
- This surge raises concerns about severe pediatric myocarditis cases.
Purpose of the Study:
- To retrospectively analyze clinical, laboratory, and imaging data of pediatric patients diagnosed with PVB19-associated myocarditis in 2024.
- To investigate the clinical presentation, severity, and outcomes of this condition.
- To explore potential links with viral coinfections and treatment responses.
Main Methods:
- Retrospective analysis of 5 pediatric patients with acute myocarditis and confirmed PVB19 DNA.
- Review of clinical symptoms, laboratory results, echocardiography findings, and treatment regimens.
- Assessment of disease severity, need for advanced support (ECMO), and patient outcomes.
Main Results:
- Patients (median age 6.4 years, 80% male) often presented with cardiogenic shock; two required ECMO.
- Echocardiography showed severely reduced ejection fraction (median 25%), atrial enlargement, and mitral insufficiency.
- PVB19 DNA load did not correlate with severity; immunomodulatory therapy showed variable results. Three patients had viral coinfections.
Conclusions:
- PVB19-associated myocarditis in children can lead to severe cardiac dysfunction, including fulminant cases.
- Immunomodulatory therapies (IVIG, corticosteroids) had variable efficacy.
- Further large-scale multicenter studies are essential to understand PVB19's role and the impact of coinfections in pediatric myocarditis.
Abstract:
Myocarditis is a significant cause of cardiac morbidity in children, with viral infections, including Parvovirus B19 (PVB19), among the most implicated agents. Recent epidemiological reports suggest a resurgence of PVB19 infections post-COVID-19, raising concerns about associated myocarditis. We aimed to retrospectively analyze clinical, laboratory, and imaging data of patients with PVB19-associated myocarditis in 2024. We included 5 pediatric patients admitted with acute myocarditis and positive blood PVB19-DNA. Median age was 6.4 years; 80% were male. Most patients presented with cardiogenic shock; two required extracorporeal membrane oxygenation. Echocardiography revealed severely reduced left ventricular ejection fraction (median 25%), atrial enlargement, and mitral insufficiency. No direct correlation was found between PVB19 DNA load and disease severity. Immunomodulatory therapy, including IVIG (intravenous immunoglobulin) and corticosteroids, was administered in most cases, with variable outcomes. Three patients had viral coinfections, raising concern for a potential link with worse outcomes. Following the SARS-CoV-2 pandemic, an apparent increase in pediatric myocarditis has been observed. The 2024 outbreak of PVB19 infections was associated with an unusual number of fulminant myocarditis cases, particularly in infants. However, our small sample precludes definitive conclusions. Larger multicenter studies are needed to clarify the role of PVB19 and coinfections in pediatric myocarditis.
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