Evidence-Based Medicine

Myocarditis

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

  1. 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
  2. Japanese Circulation Society Joint Working Group. Guidelines for diagnosis and treatment of myocarditis (JCS 2009): digest version. Circ J. 2011;75(3):734-43
  3. Sagar S, Liu PP, Cooper LT Jr. Myocarditis. Lancet. 2012 Feb 25;379(9817):738-47
  4. 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
  5. Elamm C, Fairweather D, Cooper LT. Pathogenesis and diagnosis of myocarditis. Heart. 2012 Jun;98(11):835-40

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