Assessment of Myocardial Reperfusion by Intravenous Myocardial Contrast Echocardiography and Coronary Flow Reserve After Primary Percutaneous Transluminal Coronary Angiography in Patients With Acute Myocardial Infarction

Background —This study investigated whether the extent of perfusion defect determined by intravenous myocardial contrast echocardiography (MCE) in patients with acute myocardial infarction (AMI) treated by primary percutaneous transluminal coronary angioplasty (PTCA) relates to coronary flow reserve...

Full description

Saved in:
Bibliographic Details
Published inCirculation (New York, N.Y.) Vol. 101; no. 20; pp. 2368 - 2374
Main Authors Lepper, Wolfgang, Hoffmann, Rainer, Kamp, Otto, Franke, Andreas, de Cock, Carel C., Kühl, Harald P., Sieswerda, Gertjan T., Dahl, Jürgen vom, Janssens, Uwe, Voci, Paolo, Visser, Cees A., Hanrath, Peter
Format Journal Article
LanguageEnglish
Published 23.05.2000
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background —This study investigated whether the extent of perfusion defect determined by intravenous myocardial contrast echocardiography (MCE) in patients with acute myocardial infarction (AMI) treated by primary percutaneous transluminal coronary angioplasty (PTCA) relates to coronary flow reserve (CRF) for assessment of myocardial reperfusion and is predictive for left ventricular recovery. Methods and Results —Twenty-five patients with first AMI underwent intravenous MCE with NC100100 with intermittent harmonic imaging before PTCA and after 24 hours. MCE before PTCA defined the risk region and MCE at 24 hours the “no-reflow” region. The no-reflow region divided by the risk region determined the ratio to the risk region. CFR was assessed immediately after PTCA and 24 hours later. Left ventricular wall motion score indexes were calculated before PTCA and after 4 weeks. CFR at 24 hours defined a recovery (CFR ≥1.6; n=17) and a nonrecovery group (CFR <1.6; n=8). Baseline CFR did not differ between groups. MCE ratio to the risk region was smaller in the recovery group compared with the nonrecovery group (34±49% vs 81±46%, P =0.009). A ratio to the risk region of ≤50% defined an MCE reperfusion group. It was associated with improvement of CFR from 1.67±0.47 at baseline to 2.15±0.53 at 24 hours ( P <0.001) and of regional wall motion score index from 2.6±0.5 to 1.9±0.5 at 4 weeks ( P <0.001). Conclusions —Intravenous MCE can be used to define perfusion defects after AMI. Assessment of microcirculation by MCE corresponds to evaluation by CFR. Serial intravenous MCE has the potential to identify patients likely to have improved left ventricular function after AMI.
ISSN:0009-7322
1524-4539
DOI:10.1161/01.CIR.101.20.2368