POTENTIAL CLINICAL IMPLICATIONS OF ABNORMAL MYOCARDIAL PERFUSION PATTERNS IMMEDIATELY AFTER REPERFUSION IN A CANINE MODEL - A MYOCARDIAL CONTRAST ECHOCARDIOGRAPHY STUDY
Ma. Kates et al., POTENTIAL CLINICAL IMPLICATIONS OF ABNORMAL MYOCARDIAL PERFUSION PATTERNS IMMEDIATELY AFTER REPERFUSION IN A CANINE MODEL - A MYOCARDIAL CONTRAST ECHOCARDIOGRAPHY STUDY, The American heart journal, 132(2), 1996, pp. 303-313
During myocardial infarction, lack of myocardial opacification after r
eperfusion has been associated with poor or no recovery of function. W
e have previously documented the presence of perfusion abnormalities a
fter brief coronary occlusions without infarction and the absence of p
erfusion abnormalities after prolonged occlusions with infarction. To
characterize myocardial perfusion patterns immediately after reperfusi
on, we studied 53 animals in two groups in a coronary occlusion-reperf
usion model. Temporary occlusions (group 1, 15 minutes; group 2, 30 to
360 minutes) were performed, followed by reperfusion with and without
dobutamine. Myocardial contrast echocardiography was performed with a
ortic root injections of sonicated 5% serum human albumin (Albunex) du
ring each intervention. Group 1 dogs showed no evidence of myocardial
infarction. In group 2, 26 of 40 dogs had infarctions. After reperfusi
on, no perfusion abnormalities were seen in 13 of 26 group 2 dogs with
infarctions; perfusion abnormalities were identified after reperfusio
n in 2 of 13 group 1 and in 8 of 14 group 2 dogs without infarctions.
In animals subjected to prolonged ischemia, the absence of perfusion a
bnormalities after reperfusion did not rule out the presence of necros
is. Similarly, in animals without infarction subjected to ischemia, th
e presence of a perfusion defect after reperfusion did not represent t
he presence of necrosis but an abnormal microvascular reserve. These r
esults suggest that early after reperfusion, assessment of perfusion b
y myocardial contrast echocardiography has significant limitations in
the evaluation of myocardial viability and salvage.