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Insights Into the Natural History of Recurrent Myocarditis, A Multicenter International Study (Re-Myo Study)
Chiara Baggio1,2, Antonio Cannata3,4, Alessio Gasperetti5
1Centre for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department Azienda Sanitaria Universitaria Giuliano-Isontina (ASUGI) and University of Trieste Trieste Italy.
Recurrent acute myocarditis (Re-AM) presents a distinct patient group with a worse prognosis and increased risk of arrhythmias compared to single acute myocarditis (S-AM). Understanding Re-AM characteristics is crucial for improved patient outcomes.
Area of Science:
- Cardiology
- Cardiovascular Research
- Clinical Medicine
Background:
- Recurrence of acute myocarditis (AM) poses significant clinical challenges.
- The natural history and management of recurrent AM (Re-AM) are not well-defined.
- This study aims to characterize Re-AM patients' clinical features and outcomes.
Purpose of the Study:
- To investigate the clinical characteristics of patients experiencing recurrent acute myocarditis (Re-AM).
- To compare the outcomes of Re-AM patients with those of single acute myocarditis (S-AM).
- To identify factors associated with an increased risk of recurrent AM.
Main Methods:
- An international multicenter study involving 141 patients with biopsy-proven or cardiac MRI-proven Re-AM.
- Comparison group: 372 patients with single acute myocarditis (S-AM).
- Primary outcome: composite of all-cause mortality, heart transplant, and major ventricular arrhythmias.
Main Results:
- Re-AM patients more frequently had a family history of cardiomyopathy and diffuse late gadolinium enhancement (LGE) on cardiac MRI.
- The extent of LGE increased between the first and second AM episodes in Re-AM patients.
- Re-AM patients faced a higher risk of the primary composite outcome and major ventricular arrhythmias compared to S-AM patients.
Conclusions:
- Recurrent acute myocarditis (Re-AM) represents a distinct clinical subgroup of AM.
- Re-AM is associated with a generally worse prognosis and a specific increased arrhythmic risk compared to S-AM.
- Family history of cardiomyopathy, autoimmune diseases, and ring-like LGE are independently associated with higher Re-AM risk.
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