In this post, I link to and excerpt the article, Viral Myocarditis from StatPearls [Link is to the complete StatPearls Table of Contents]
Michael Kang1; Jason An2.
1 University of California Riverside School of Medicine
2 Riverside Community Hospital/UCRiverside
Last Update: August 11, 2020.
All that follows are excerpts from Viral Myocarditis:
Pearls and Other Issues
All patients diagnosed or suspected to have acute myocarditis should be admitted to the hospital and be monitored for hemodynamic instability. Immediate complications of myocarditis include ventricular dysrhythmias, left ventricular aneurysm, CHF, and dilated cardiomyopathy. The mortality rate is up to 20% at 1 year and 50% at 5 years. Despite optimal medical management, overall mortality has not changed in the last 30 years.
Myocarditis is an inflammatory process of the myocardium. It can present as an acute, subacute, or chronic disease process and may present with either focal or diffuse involvement of the myocardium. In symptomatic patients, the presentation can be highly variable from generalized fatigue, malaise, chest pain, congestive heart failure (CHF), cardiogenic shock, arrhythmias and even cardiac arrest.
In the United States and other developed countries, viral infections are most frequently the cause of myocarditis. In developing countries, rheumatic carditis, Chagas disease, and complications related to advanced HIV/AIDS also provide important causes of myocarditis. Other causes include toxic myocarditis, which is related to drugs that may cause an insidious form of the disease.
Myocarditis is diagnosed based on clinical presentation. Diagnosis is classically confirmed by endomyocardial biopsy (EMB) via established histologic, immunologic, and immunohistochemical criteria.
Myocarditis can occur in another wise healthy person and quickly result in progressive heart failure. Myocarditis my be acute (first 2 weeks) or chronic (lasting more than 2 weeks).
The etiology is thought to be caused by a variety of infectious and non-infectious causes. Among the infectious causes, viruses are presumed to be the most common pathogen. In North America and Europe the most frequently implicated viruses include enteroviruses, including coxsackievirus. Parvovirus B-19 and human herpesvirus 6 are frequent culprits as well. Other pathogens that have been implicated include various bacteria, fungi, protozoa, and helminths. Other common but non-infectious causes of myocarditis include autoimmune disorders such as systemic lupus erythematosus (SLE), Wegener’s granulomatosis, and giant cell arteritis. In almost 50-80% of cases, no cause is ever found. In some of these patients, viral particles may be found in biopsy specimens.
The incidence of myocarditis is approximately 1.5 million cases worldwide per year. Incidence is usually estimated between 10 to 20 cases per 100,000 persons. The overall incidence is unknown and probably underdiagnosed. In the United States, the frequency of myocarditis is difficult to ascertain as many cases are subclinical. In community-based populations, the prevalence and outcomes of myocarditis are unknown as epidemiologic studies suggest that the majority of Coxsackie B virus infections, an important cause of myocarditis are subclinical, thus following a benign course.
According to some estimates, 1% to 5% of all patients with acute viral infections may involve the myocardium.
The majority of patients are young and healthy. Individuals who are susceptible include children, pregnant women and those who are immunocompromised.
History and Physical
Patients typically will present with a 7-14 day history of a flu-like illness, including fever, malaise, myalgia, vomiting, and diarrhea.
- Adults will typically present with dyspnea, chest pain, and arrhythmias. Vital signs will be abnormal, including fever, tachycardia, tachypnea and sometimes hypotension. No single sign or symptom will be specific to make the diagnosis, but a presentation with chest pain or CHF often indicates a poor prognosis.
- Children will often present with grunting respirations and intercostal retractions. Infants will often present with the fulminant syndrome, fever, hypoxia with cyanosis, respiratory distress/failure, and even cardiac arrest. Much like adults, long-term prognosis correlates with the severity of their initial presentation.
Most patients will present with abnormal ECG that are widely variable. This included sinus tachycardia, widened QRS patterns, low voltage, prolonged QT, variable atrioventricular (AV) blocks, and even acute myocardial infarction (AMI) pattern.
Cardiac markers, such as troponin, may be elevated, but during which course of the disease process is mostly unknown. Higher levels of troponin likely correlate with more myocardial damage as it is indicative of myonecrosis, but negative values do not rule out the diagnosis. Other tests that should be ordered include complete blood count (CBC), erythrocyte sedimentation rate (ESR), and c-reactive protein (CRP). The white count, ESR, and CRP may be elevated but are not diagnostic in any way.
Viral antibody titers should also be ordered and should include coxsackievirus group B, HIV, CMV, Ebstein-Barr virus, hepatitis and influenza viruses. Titers will typically increase by four-fold during the acute phase with gradual fall with the progression of the disease process. Serial titers may be helpful.
Cardiac ECHO should be ordered and may show nonspecific findings such as reduced left the ventricular function, global hypokinesis, and even regional wall motion abnormalities.
Contrast MRI or nuclear studies can show the extent of the inflammation and cellular edema, although this may still be non-specific.
Endomyocardial biopsy (EMB), while considered the “gold standard” for diagnosis, is rarely utilized as it has limited sensitivity and specificity, as inflammation across the myocardium may be diffuse or focal in myocarditis. More importantly, histologic diagnosis rarely has an impact on therapeutic approaches. However, if a patient is deteriorating and no cause if found, the Heart Failure Society of America does recommend a myocardial biopsy.
In some patients, cardiac catheterization may be required to rule out coronary artery disease.
Treatment / Management
Patients who presently acutely need to be managed with supplemental oxygen and optimization of fluid status. Beta blockers should be avoided in those with heart block and heart failure. Patients with a heart block may require a temporary pacemaker. Some patients may require an AICD.
Those patients with heart failure often require diuretics and inotropic support. Log term treatment with ACE inhibitors is recommended. All cardiotixic drugs should be withheld. NSAIDs should be withheld as they impede healing of the myocardium and exacerbate the inflammatory process. Some patients may require anticoagulation. The use of antiarrhythmics requires good clinical judgment as many of these agents also have negative inotropic effects that may aggravate heart failure.
Treatment, for the most part, is supportive and aimed at preserving left ventricular function and can range from a simple limitation of activity to rhythm and CHF management, ventricular assist devices and even cardiac transplantation down the road. Multicenter trials evaluating immunosuppressive therapies have shown no benefit at this time. In the chronic stage, CHF symptoms tend to predominate, and standard pharmacologic treatments for CHF are indicated.
Some patients may benefit from short term use of the intra-aortic balloon pump and or ventricular assist device. Cardiac transplantation is an option if a donor can be found.
Patients with mild symptoms do improve spontaneously but recovery can take months. Repeat assessment with echocardiograms is necessary. Patients who continue to do poor should be referred to a tertiary care center where transplant and assist device services are available.
- Carnitine deficiency
- Coarctation of the aorta
- Coronary artery anomalies
- Cardiac tumour
- Dilated cardiomyopathy
- Endocardial fibroelastosis
- Enteroviral infections
- Genetics of von Gierke disease
- Genetics of glycogen-storage disease type II
- Medial necrosis of coronary arteries
- Nonviral myocarditis
- Valvar aortic stenosis
- Viral pericarditis
The prognosis of patients with myocarditis depends on the severity of the inflammatory process and presentation of symptoms. Patients with severe disease have a poor prognosis without a transplant. Patients with mild myocarditis usually have a good outcome. Poor prognostic factors include low ejection fraction, left bundle branch block and syncope. The most common cause of death is cardiogenic shock. Others may develop varying degrees of heart block that requires permanent pacing. The highest mortality rates are seen in postpartum cardiomyopathy.*
*Postpartum Cardiomyopathy from StatPearls
Ateeq Mubarik1; Venu Chippa2; Arshad Muhammad Iqbal3.
1 Oak hill hospital
2 Indiana university
3 Oak Hill Hospital, Brooksville, FL
Last Update: March 28, 2021.