Differences between genetic dilated cardiomyopathy and myocarditis in children presenting with severe cardiac dysfunction.
Ferran GranAndrea FidalgoPaola DoladerMarta GarridoAlexandra NavarroJaume Izquierdo-BlascoJoan BalcellsMarta Codina-SolaPaula Fernandez-AlvarezAnna Sabaté-RotésPedro BetriánJoaquín Fernández-DoblasRaúl AbellaFerran Roses-NoguerPublished in: European journal of pediatrics (2021)
Acute myocarditis is an inflammatory disease of the myocardium, and it can present as severe heart failure in children. Differential diagnosis with genetic cardiomyopathy can be difficult. The objective of this study is to identify patterns of clinical presentation and to assess invasive and non-invasive measures to differentiate patients with acute myocarditis from patients with dilated genetic cardiomyopathy. We performed a retrospective descriptive study of all paediatric patients (0-16 years old) that presented with new-onset heart failure with left ventricle ejection fraction < 35% in whom we performed an endomyocardial biopsy (EMB) during the period from April 2007 to December 2020. The patients were classified into two groups: Group 1 included 18 patients with myocarditis. Group 2 included 9 patients with genetic cardiomyopathy. Findings favouring a diagnosis of myocarditis included a fulminant or acute presentation (77.8% vs 33.3%, p = 0.01), higher degree of cardiac enzyme elevation (p = 0.011), lower left ventricular dimension z-score (2.2 vs 5.4, p = 0.03) increase of ventricular wall thickness (88.8% vs 33.3%, p = 0.03) and oedema in the EMB. Seven (77.8%) patients with genetic cardiomyopathy had inflammation in the endomyocardial biopsy fulfilling the diagnostic criteria of inflammatory cardiomyopathy.Conclusion: Differentiating patients with a myocarditis from those with genetic cardiomyopathy can be challenging, even performing an EMB. Some patients with genetic cardiomyopathy fulfil the diagnostic criteria of inflammatory cardiomyopathy. Using invasive and non-invasive measures may be useful to develop a predictive model to differentiate myocarditis from genetic cardiomyopathy. What is Known: • Acute myocarditis could present with cardiogenic shock in paediatric patients. • Parvovirus B19 is the main cause of myocarditis in this population. What is New: • Current diagnostic criteria for myocarditis have limited use in paediatric patients presenting with new-onset heart failure. • Some patients with a genetic cardiomyopathy and a new-onset heart failure fulfill the diagnostic criteria of inflammatory cardiomyopathy.
Keyphrases
- heart failure
- ejection fraction
- left ventricular
- end stage renal disease
- genome wide
- aortic stenosis
- cardiac resynchronization therapy
- chronic kidney disease
- oxidative stress
- newly diagnosed
- intensive care unit
- atrial fibrillation
- liver failure
- acute heart failure
- drug induced
- young adults
- emergency department
- peritoneal dialysis
- patient reported outcomes
- dna methylation
- coronary artery disease
- prognostic factors
- magnetic resonance imaging
- left atrial
- pulmonary artery
- mechanical ventilation
- aortic valve
- fine needle aspiration