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Myocardial perfusion abnormalities by intravenous administration of the contrast agent NC100100 in an experimental model of coronary artery occlusion and reperfusion
CNR, Institute of Clinical Physiology, Pisa, Italy.
Linköping University, Department of Biomedical Engineering, Physiological Measurements. Linköping University, The Institute of Technology. Östergötlands Läns Landsting, Heart and Medicine Centre, Department of Clinical Physiology UHL.
Gottsegen György Hungarian Institute of Cardiology, Budapest, Hungary.
CNR, Institute of Clinical Physiology, Pisa, Italy.
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1998 (English)In: Echocardiography, ISSN 0742-2822, E-ISSN 1540-8175, Vol. 15, no 8, 731-740 p.Article in journal (Refereed) Published
Abstract [en]

The aim of this study was to evaluate a second-generation echo contrast agent (NC100100) for the study of myocardial perfusion. In eight anesthetized open-chest dogs, this agent was injected intravenously under baseline conditions, during acute coronary thrombosis, and after reperfusion, using both fundamental (FI) and harmonic (HI) imaging, both continuous and intermittent imaging, and both ultrasound (US) and integrated backscatter (IBS) imaging. Contrast injections did not modify the hemodynamic parameters. With all imaging modalities, myocardial contrast enhancement (MCE) was higher with intermittent than with continuous imaging (134 vs 82 gray level/pixel using FI, P = 0.02; 62 vs 32 acoustic units using US HI, P = 0.02; and 52 vs 12 dB using IBS, P = 0.05). MCE equally increased using either US or IBS imaging. The accuracy of MCE in detecting perfusion defects during coronary occlusion and myocardial reperfusion after thrombolysis was very good (sensitivity and specificity = 93% and 95% and 89% and 93%, respectively). The extent of myocardial perfusion defects by echo contrast showed a closer correlation with microspheres using HI (r = 0.82) than FI (r = 0.53). Thus, the intravenous administration of NC100100 during intermittent HI allows myocardial perfusion abnormalities to be accurately detected during acute myocardial infarction.

Place, publisher, year, edition, pages
1998. Vol. 15, no 8, 731-740 p.
National Category
Medical Laboratory and Measurements Technologies
URN: urn:nbn:se:liu:diva-67489DOI: 10.1111/j.1540-8175.1998.tb00673.xPubMedID: 11175105OAI: diva2:410591
Available from: 2011-04-14 Created: 2011-04-14 Last updated: 2011-05-03

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