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Published on: February 10, 2023
Neonatal Enterovirus Myocarditis With Severe Dystrophic Calcification: Novel Treatment With Pocapavir
Samuel G Wittekind1, Catherine C Allen1, John L Jefferies1
1Cincinnati Children's Hospital Medical Center and University of Cincinnati, Cincinnati, OH, USA.
Insights
This study details a neonate with enterovirus myocarditis and dystrophic calcification. Treatment with pocapavir improved heart function, though calcification remained.
Area of Science:
- Cardiology
- Virology
- Neonatal Medicine
Background:
- Dystrophic myocardial calcification is linked to myocardial injury with normal serum calcium.
- Enterovirus myocarditis can cause severe left ventricular systolic dysfunction in neonates.
Purpose of the Study:
- To report a case of neonatal enterovirus myocarditis with significant dystrophic calcification.
- To evaluate the efficacy of the antiviral pocapavir in this context.
- To highlight imaging findings and treatment outcomes.
Main Methods:
- Case presentation of a neonate with enterovirus myocarditis.
- Utilized multiple imaging modalities to assess cardiac function and calcification.
- Administered pocapavir combined with a standard heart failure regimen.
Main Results:
- The neonate presented with prominent dystrophic myocardial calcification and severe left ventricular systolic dysfunction.
- Following treatment with pocapavir and standard care, significant left ventricular remodeling occurred.
- Dystrophic calcification persisted despite clinical improvement.
Conclusions:
- Pocapavir may be a viable treatment option for enterovirus myocarditis in neonates, contributing to cardiac remodeling.
- This case represents the first reported use of pocapavir for enterovirus-induced myocardial calcification.
- Further research is warranted to explore pocapavir's role in managing viral myocarditis and associated complications.
Abstract:
Dystrophic myocardial calcification occurs in the setting of myocardial injury and normal serum calcium. We present a case of a neonate with prominent dystrophic calcification and severe left ventricular systolic dysfunction in the setting of enterovirus myocarditis. These findings are superbly illustrated by multiple imaging modalities. The patient was treated with the novel antiviral, pocapavir, in addition to a standard heart failure regimen. The dystrophic calcification persisted but the left ventricle remodeled significantly. To our knowledge, this is the first reported use of pocapavir for this indication. The literature regarding enterovirus myocarditis and pocapavir is briefly reviewed.
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