F. Leclercq et al., LOW-DOSE DOBUTAMINE ECHOCARDIOGRAPHIC ASS ESSMENT OF REVERSIBLE CONTRACTILE DYSFUNCTION (MYOCARDIAL STUNNING) AFTER MYOCARDIAL-INFARCTION, Archives des maladies du coeur et des vaisseaux, 91(3), 1998, pp. 331-336
Low dose (5 to 10 mu g/min) dobutamine echocardiography was used to pr
edict the presence of reversible contractile dysfunction (myocardial s
tunning) after myocardial infarction successfully revascularised in th
e acute phase of primary angioplasty. The investigation was undertaken
in 40 patients, 4 +/- 1 days after inaugural myocardial infarction. T
he left ventricle was divided into 16 segments. Viable myocardium was
diagnosed when the initial regional wall motion score decreased by at
least 2. Resting echocardiography was performed at 2 months to evaluat
e the effective recovery of regional wall motion (myocardial viability
). The presence of contractile reserve was documented by dobutamine ec
hocardiography in 18 patients (45 %). The sensitivity, specificity and
positive and negative predictive values of dobutamine echocardiograph
y for the diagnosis of myocardial viability were 82, 83, 78 and 86 % r
espectively. The negative predictive value was high in all dysynergic
segments (86 %). The positive predictive value of the investigation wa
s however higher in hypokinetic than in akinetic segments (73 vs 21 %;
p < 0.05). The recovery of regional wall motion during follow-up was
statistically related to higher initial left ventricular ejection frac
tion (p < 0.04), the presence of angiographically documented collatera
l circulation before revascularisation (p = 0.007), the contractile re
sponse to dobutamine (p = 0.0001) and was observed more frequently in
hypokinetic than in akinetic segments (p < 0.05). These results show t
hat low-dose dobutamine echocardiography is a sensitive and specific i
nvestigation for predicting irreversible myocardial damage after succe
ssful primary angioplasty in acute myocardial infarction. However, eve
n in the absence of residual coronary stenosis, the presence of viable
myocardium is only identified specifically in hypokinetic segments.