About this trial
The goal of this observational study is to determine the efficacy a of combined management and treatment driven by the systematic determination of viral genome, bacterial serology, and markers of inflammation in pediatric patients (\< 18 years old) diagnosed with myocarditis complicated by arrhythmias (supraventricular and ventricular tachycardias and heart block) or ventricular dysfunction (left ventricular ejection fraction \< 50% or right ventricular fractional area change \< 35%).
The main question it aims to answer is: Does this panel help resolve arrhythmias or myocardial dysfunction due to myocarditis during hospitalisation and follow-up?
Researchers will compare patients managed and treated in 2024 without applying the myocarditis panel with those enrolled in 2025 who received the panel. Arrhythmias and myocardial dysfunction will be managed in accordance with recent guidelines. Antiviral, antibiotic or immunosuppressive therapies will be implemented in addition to standard therapy when required by the panel.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
All the consecutive pediatric patients (< 18 years old) presenting with myocarditis complicated by arrhythmias or myocardial dysfunction
Disqualifiers
Refused consent to be included in the study given by parents or legal tutors
Uncomplicated myocarditis presenting without arrhythmias or myocardial dysfunction
Trial design
Crossover
Treatments tested in this trial
Determination of viral genome, bacterial serology, and markers of inflammation in pediatrics diagnosed with myocarditis
Diagnostic testN=15 patients from 2025, in which management and treatment of arrhythmias and or myocardial dysfunction were driven by the panel
Treatment groups
Trial outcomes
Primary outcomes
Arrhythmias duration
Total duration of in-hospital arrhythmias assessed by electrocardiography
Myocardial dysfunction
Total duration of myocardial dysfunction assessed by echocardiography
Secondary outcomes
Follow-up
Recurrences of arrhythmias or myocardial dysfunction at the follow-up
Sponsors and contacts
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