Myocarditis
Myocarditis
🠶 The inflamed myocardium is soft, flabby, and pale, with areas of scarring on gross
examination.
🠶 Rarely, bacteria, rickettsia, fungi, protozoa, and parasites are the causative agents.
PHYSICAL EXAMINATION
🠶 Presentation depends on the patient’s age and the acute or chronic nature of the infection.
🠶 In neonates and infants, signs of CHF may be present; these include poor heart tone,
tachycardia, gallop rhythm, tachypnea, and (rarely) cyanosis. In older children, a gradual
onset of CHF and arrhythmia are commonly seen.
🠶 A soft, systolic heart murmur and irregular rhythm caused by supraventricular or ventricular
ectopic beats may be audible.
🠶 Hepatomegaly (evidence of viral hepatitis) may be present.
DIAGNOSIS
CXR :Radiography: Cardiomegaly of varying degrees is the most important clinical sign of
myocarditis
Electrocardiography
🠶 low QRS voltages, ST-T changes,
🠶 PR prolongation, prolongation of the QT interval, and
🠶 arrhythmias (especially premature contractions).
Echocardiography
🠶 Echocardiography reveals cardiac chamber enlargement and
🠶 impaired left ventricle (LV) function, often regional in nature.
🠶 Occasionally, increased wall thickness and LV thrombi are found.
Laboratory Studies:Cardiac troponin levels (troponin I and T) and myocardial enzymes (creatine
kinase [CK], MB isoenzyme of CK [CK-MB]) may be elevated. In children, the normal value of
cardiac troponin I has been reported to be 2 ng/mL or less, and it is frequently below the level of
detection for the assay. Troponin levels may be more sensitive than the cardiac enzymes.
Radionuclide scanning (after administration of gallium-67 or technetium-99m pyrophosphate) may
identify inflammatory and necrotic changes characteristic of myocarditis.
Endomyocardial biopsy. Myocarditis can be confirmed
Natural History
🠶 Mortality rate is as high as 75% in symptomatic neonates with acute viral
myocarditis.
🠶 Some patients develop subacute or chronic myocarditis with persistent cardiomegaly (with
or without signs of CHF) and ECG evidence of left ventricular hypertrophy (LVH) or
biventricular hypertrophy (BVH). Clinically, these patients are indistinguishable from those
with dilated cardiomyopathy.