Key result
Percutaneous Embozene microspheres reliably produce nonreperfused swine MI with ~23% mortality.
Why the study?
Modeling nontreated nonreperfused myocardial infarction is important for developing and preclinical testing of new therapies for patients missing the revascularization time window after MI.
Percutaneous injection of Embozene microspheres successfully generates a nonreperfused myocardial infarction model in swine that is fully compatible with MRI evaluation.
Answers are grounded in this paper and cite their sources.
Supports swine modeling of nonreperfused MI; leaves open translation to clinical therapeutic testing.
OBJECTIVES: To develop a magnetic resonance imaging (MRI) compatible, percutaneous technique for the generation of nonreperfused myocardial infarct (MI). BACKGROUND: Modeling nontreated MI has major importance in the development and preclinical testing of new therapeutic strategies for patients missing the time window suitable for revascularization following MI. METHODS: In 31 male swine, nonreperfused MI was generated by permanent occlusion of either the LAD or LCX coronary artery using 900 μm Embozene™ microspheres. Animals were monitored for 90 min postocclusion. Surviving animals were followed up for 2 (n = 6), 4 (n = 6), 14 (n = 6), or 56 (n = 6) days. At the end of the planned study session, contrast enhanced MRI, triphenyl-tetrazolium-chloride staining, and microscopic histopathology were carried out. RESULTS: The mortality rate in this study was 22.6%. Intraoperative arrhythmias occurred in 14 cases: premature ventricular complexes with (5) or without (3) ventricular tachycardia, 2nd degree atrio-ventricular block (1), and ventricular fibrillation (6). MRI, TTC, and histology confirmed the existence of MI in every case. Macroscopic pathology showed that the microspheres caused a practically total occlusion at the epicardial level of the coronary artery. Multiple infarcts were detected in one case, probably due to unintentional reflux of the microspheres. Microspheres retained in the coronary arteries did not cause any MRI artifact. CONCLUSIONS: The generation of nonreperfused MI is feasible by percutaneous injection of Embozene into the coronary artery system. The MI model thus obtained is suitable for the purposes of MRI experiments.
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Varga‐Szemes et al. (2012) studied Nonreperfused myocardial infarction (n=31). Embozene™ microspheres was evaluated on Mortality rate. Percutaneous injection of 900 μm Embozene microspheres successfully generated MRI-compatible nonreperfused myocardial infarction in a swine model, with a 22.6% mortality rate.
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