Evidence-Based Medicine
Myocarditis
Background
- Myocarditis is an inflammation of the myocardium secondary to pathologic immune processes that are triggered by a variety of underlying etiologies (such as infection [including HIV and Zika], autoimmune disease, drug reactions, or peripartum syndromes).
Evaluation
- Suspect myocarditis in patients with new-onset myocardial injury resulting in electrical or mechanical abnormalities in cardiac function in absence of acute coronary syndromes or other causes.
- Patients commonly present with nonspecific symptoms including chest pain, dyspnea, and palpitations.
- Myocarditis is often part of a pancarditis involving the epicardium, pericardium, and endocardium and may present with pericarditis, worsening heart failure, atrial or ventricular arrhythmias, valvular dysfunction, heart block, cardiogenic shock, or sudden cardiac death.
- Perform an echocardiography to assess ventricular size and function to rule out other causes of cardiac dysfunction (Strong recommendation).
- Consider obtaining cardiac magnetic resonance (CMR) to distinguish ischemic from nonischemic cardiomyopathy.
- Consider measuring serum biomarkers such as cardiac troponin where elevated levels are supportive but not diagnostic of myocarditis.
- Perform an endomyocardial biopsy in patients with (Strong recommendation):
- new-onset heart failure of < 2 weeks with normal-sized or dilated left ventricle and hemodynamic compromise (suspected fulminant lymphocytic myocarditis)
- new-onset heart failure of 2 weeks to 3 months with dilated left ventricle and new ventricular arrhythmias, second- or third-degree heart block, or failure to respond to usual care in 1-2 weeks (suspected giant cell myocarditis)
Management
- Provide standard pharmacologic and supportive medical care for a patient presenting with heart failure (Strong recommendation).
- Do not routinely use immunosuppressive therapy (Strong recommendation).
- Consider a trial of immunosuppressive therapy for children and patients with (Weak recommendation):
- giant cell myocarditis
- autoimmune or hypersensitivity myocarditis
- severe hemodynamic compromise and deteriorating conditions
- cardiac sarcoidosis
- eosinophilic myocarditis
- nonviral myocarditis
- Refer patients with suspected myocarditis to a specialty center (Strong recommendation).
- Refer patients for cardiac transplantation evaluation or mechanical circulatory support if they have:
- heart failure and evidence of end-organ damage or progressive deterioration (refer urgently) (Strong recommendation)
- severe heart failure despite standard heart failure therapy (Strong recommendation)
Published: 01-07-2023 Updeted: 01-07-2023
References
- Howlett JG, McKelvie RS, Arnold JM, et al. Canadian Cardiovascular Society Consensus Conference guidelines on heart failure, update 2009: diagnosis and management of right-sided heart failure, myocarditis, device therapy and recent important clinical trials. Can J Cardiol. 2009 Feb;25(2):85-105
- Japanese Circulation Society Joint Working Group. Guidelines for diagnosis and treatment of myocarditis (JCS 2009): digest version. Circ J. 2011;75(3):734-43
- Sagar S, Liu PP, Cooper LT Jr. Myocarditis. Lancet. 2012 Feb 25;379(9817):738-47
- Friedrich MG, Sechtem U, Schulz-Menger J, et al; International Consensus Group on Cardiovascular Magnetic Resonance in Myocarditis. Cardiovascular magnetic resonance in myocarditis: A JACC White Paper. J Am Coll Cardiol. 2009 Apr 28;53(17):1475-87
- Elamm C, Fairweather D, Cooper LT. Pathogenesis and diagnosis of myocarditis. Heart. 2012 Jun;98(11):835-40