Myocarditis Treatment
All patients with definite myocarditis should be hospitalized, ideally at an advanced heart failure center, and treated with guideline-directed medical therapy for heart failure, while immunosuppression is generally NOT indicated except for specific subtypes like giant cell myocarditis, cardiac sarcoidosis, or eosinophilic myocarditis. 1, 2
Immediate Hospitalization and Risk Stratification
- Hospitalize all patients with mild or moderate myocarditis at an advanced heart failure center 3, 1
- Transfer patients with fulminant myocarditis (hemodynamic instability, cardiogenic shock, or refractory arrhythmias) to centers with expertise in mechanical circulatory support 3, 1, 2
- Fulminant myocarditis carries 28% mortality at 60 days despite aggressive treatment, but paradoxically has better long-term prognosis than non-fulminant forms if patients survive the acute phase 2, 4
Standard Medical Therapy (First-Line for All Patients)
Initiate guideline-directed heart failure therapy before discharge and titrate in outpatient setting: 3, 1, 2
- ACE inhibitors or ARBs for neurohormonal blockade (start with low doses like captopril 1-6.25 mg if systolic BP >100 mmHg) 2, 4
- Beta-blockers for patients with supraventricular arrhythmias, but ONLY if hemodynamically stable—avoid in overt heart failure with pulmonary congestion or low output 1, 2, 4
- Aldosterone antagonists for patients with mildly reduced left ventricular function and stable hemodynamics 1
Critical Pitfall: Avoid NSAIDs
- Do NOT use NSAIDs for chest pain in myocarditis (except when pericardial involvement is suspected), as they increase inflammation and mortality in animal models 3
- For pericardial involvement specifically, NSAIDs, colchicine, and/or prednisone are reasonable 3
Mechanical Circulatory Support for Severe Cases
For patients with cardiogenic shock despite optimal medical management: 3, 1, 2
- Start inotropic support (dopamine 5 mcg/kg/min, titrate up to 20-50 mcg/kg/min based on response) 4
- Initiate mechanical circulatory support urgently if shock does not reverse rapidly with pharmacological therapy 4
- Options include percutaneous cardiopulmonary support, ECMO, or intra-aortic balloon pump 2, 4
- Some patients can be bridged to recovery; cardiac transplantation survival rates are similar to other causes of heart failure 3, 1
Immunosuppression: Only for Specific Subtypes
Immunosuppression is generally NOT indicated for acute lymphocytic myocarditis in adults (the most common form), as individual trials and meta-analyses show no benefit 3, 1, 2
When to Use Immunosuppression:
Consider immunosuppressive therapy in these specific circumstances: 3, 1, 2
- Giant cell myocarditis (requires immunosuppression)
- Cardiac sarcoidosis (requires immunosuppression)
- Eosinophilic myocarditis (requires immunosuppression)
- COVID-19 myocarditis with hemodynamic compromise or MIS-A: IV corticosteroids may be considered 3
- COVID-19 myocarditis with pneumonia requiring supplemental oxygen: treat with corticosteroids 3, 1
- Biopsy-proven severe myocardial inflammatory infiltrates or fulminant myocarditis: empiric corticosteroids may be considered, balanced against infection risk 3, 1
For immune checkpoint inhibitor-induced myocarditis (grade 3-4): 2
- Permanently discontinue the immunotherapy
- Start high-dose methylprednisolone 1 mg/kg IV immediately
- Continue for several days until improvement to grade ≤1
- Mortality remains high at 23% despite rapid treatment
Arrhythmia Management
- Acute arrhythmias often resolve with resolution of inflammation—management is supportive 3
- Continuous ECG monitoring is essential 4
- Insert temporary pacemaker if symptomatic or high-grade AV block triggers ventricular tachyarrhythmias 4
- Consider permanent pacemaker if AV block persists 4
- For drug-refractory ventricular arrhythmias after myocarditis, endocardial and epicardial radiofrequency catheter ablation can be effective 3
Activity Restriction
Mandate complete exercise abstinence for 3-6 months after diagnosis 3, 1
- Sustained aerobic exercise during acute viral myocarditis increases mortality in animal models and can cause sudden death 3
- Competitive sport participation should be avoided for 3-6 months 3, 1
- Before resuming competitive sports, reassess with: 3
- Absence of cardiopulmonary symptoms
- Resolution of laboratory evidence of myocardial injury
- Normalization of LV systolic function
- Absence of spontaneous/inducible cardiac arrhythmias on ECG monitoring and exercise stress testing
Follow-Up Surveillance
Perform follow-up testing 3-6 months after presentation to assess recovery: 1, 2