Key result
Investigational treatments for myocarditis include immunosuppressants and antivirals, but improved early detection and differentiation between viral and autoimmune etiologies are required.
This review highlights the current standard of care and investigational treatments for myocarditis, emphasizing the critical need for early detection and etiology-specific management.
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Standard myocarditis care should continue without investigational agents; leaves open the need for trials validating early etiology-specific detection.
Myocarditis is a common cause of cardiomyopathy and is thought to account for 25% of all cases in humans. Unfortunately, the disease is difficult to detect clinically before a myopathic process ensues. Management of myocarditis-induced heart failure includes the standard regimen of diuretics, digoxin, angiotensin-converting enzyme inhibitors, angiotensin-II receptor blockers, and beta-adrenergic blockers. The management of myocarditis itself is dependent on the etiology of the illness. Treatments that are currently under investigation include immunosuppressants, nonsteroidal antiinflammatory agents, immunoglobulins, immunomodulation, antiadrenergics, calcium-channel blockers, angiotensin-converting enzyme inhibitors, nitric oxide inhibitors (e.g., aminoguanidine), and antivirals. Despite advances in treatment, more work needs to be done in the early detection of myocarditis. Additionally, better means need to be established for distinguishing between viral and noninfectious autoimmune forms of the disease, so that appropriate treatment can be instituted.
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Frishman et al. (2002) conducted a review in Viral and Autoimmune Myocarditis. Investigational treatments (immunosuppressants, antivirals, immunomodulators) was evaluated. Investigational treatments for myocarditis include immunosuppressants and antivirals, but improved early detection and differentiation between viral and autoimmune etiologies are required.
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