Evaluation of stunned and infarcted canine myocardium by real time myocardial contrast echocardiography

P.M.M. Dourado, J.M. Tsutsui, W. Mathias Jr., J.L. Andrade, P.L. da Luz, A.C.P. Chagas
2003 Brazilian Journal of Medical and Biological Research  
Differentiation between stunned and infarcted myocardium in the setting of acute ischemia is challenging. Real time myocardial contrast echocardiography allows the simultaneous assessment of myocardial perfusion and function. In the present study we evaluated infarcted and stunned myocardium in an experimental model using real time myocardial contrast echocardiography. Sixteen dogs underwent 180 min of coronary occlusion followed by reperfusion (infarct model) and seven other dogs were
more » ... dogs were submitted to 20 min of coronary occlusion followed by reperfusion (stunned model). Wall motion abnormality and perfusional myocardial defect areas were measured by planimetry. Risk and infarct areas were determined by tissue staining. In the infarct model, the wall motion abnormality area during coronary occlusion (5.52 ± 1.14 cm 2 ) was larger than the perfusional myocardial defect area (3.71 ± 1.45 cm 2 ; P < 0.001). Reperfusion resulted in maintenance of wall motion abnormality (5.45 ± 1.41 cm 2 ; P = 0.43 versus occlusion) and reduction of perfusional myocardial defect (1.51 ± 1.29 cm 2 ; P = 0.004 versus occlusion). Infarct size determined by contrast echocardiography correlated with tissue staining (r = 0.71; P = 0.002). In the stunned model, the wall motion abnormality area was 5.49 ± 0.68 cm 2 during occlusion and remained 5.1 ± 0.63 cm 2 after reperfusion (P = 0.07). Perfusional defect area was 2.43 ± 0.79 cm 2 during occlusion and was reduced to 0.2 ± 0.53 cm 2 after reperfusion (P = 0.04). 2,3,5-Triphenyl tetrazolium chloride staining confirmed the absence of necrotic myocardium in all dogs in the stunned model. Real time myocardial contrast echocardiography is a noninvasive technique capable of distinguishing between stunned and infarcted myocardium after acute ischemia.
doi:10.1590/s0100-879x2003001100009 pmid:14576906 fatcat:fywnrrosgnhoznkcbyu2efrti4