cute myocarditis is diagnosed when the heart is involved in an acute inflammatory process caused by infectious agents (eg, viruses). The clinical manifestation ranges from the asymptomatic state to fulminant heart failure. Acute viral myocarditis is entirely selflimiting and often unrecognized, but in some patients, the myocarditis culminates in dilated cardiomyopathy as a consequence of viral-mediated immunological chronic myocardial damage. In others, viral myocarditis rapidly progresses to critical fulminant state and requires aggressive pharmacologic and mechanical support. 1 It is therefore clinically important to determine whether the myocardial damage is transient or persistent. Endomyocardial biopsy is currently used to confirm the diagnosis of myocarditis, but it is invasive and a borderline or negative biopsy can not exclude the diagnosis. Echocardiographic integrated backscatter (IB) attempts to identify myocardial pathology from changes in myocardial acoustic properties and has been used to evaluate ischemic heart disease, 2-5 cardiomyopathies, 6,7 cardiac allograft rejection 8,9 and diabetic hearts. 10 In acute myocardial infarction, the cardiac cycle-dependent variation of myocardial IB (cyclic variation of IB, CV-IB) is reduced, but after reperfusion therapy, the blunted CV-IB recovers earlier than the improvement of left ventricular (LV) asynergy. 2 It is therefore uncertain whether IB analysis can also predict LV functional recovery in acute myocarditis, so we measured the serial changes in the systolic echo parameters and CV-IB in a young adult patient with acute myocarditis.
MethodsConventional echocardiography and IB analysis were carried out. LV end-diastolic and end-systolic dimensions and posterior wall thickness were measured as recommended by the American Society of Echocardiology 11 and fractional shortening and systolic posterior wall thickening were calculated. The IB study was performed using a modified commercially available system (Toshiba SSA 250A, Toshiba Medical Co, Tokyo, Japan) equipped with a 3.75 MHz broadband transducer, which enabled us to quantify the backscatter energy returned from the myocardium in M-mode format. A parasternal LV long or short axis view at the chordal level was obtained, in which the M-mode cursor line was perpendicular to the myocardial fiber orientation of the posterior wall. The native raw radiofrequency signal was sampled with a digital oscilloscope (Sony Tektronix TDS 754A, Sony Tektronix Co, Tokyo) at a sampling rate of 2 GHz with 8-bit resolution. For analysis of the myocardium, the radiofrequency signal was electronically gated from the intramural region of the LV posterior wall to avoid epicardial and endocardial specular reflections. The sample gate width was set to 2.5 s, which corresponds to 2.0 mm, given that the velocity of ultrasound in biological tissue is 1.57 mm/ s. Power spectral analysis of the gated data was determined by fast Fourier transformation with a Hanning window. Signal sampling and power spectral analysis were performed e...