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Case Reports
. 2005;32(4):598-601.

Myoangiogenesis after cell patch cardiomyoplasty and omentopexy in a patient with ischemic cardiomyopathy

Affiliations
Case Reports

Myoangiogenesis after cell patch cardiomyoplasty and omentopexy in a patient with ischemic cardiomyopathy

Syde A Taheri et al. Tex Heart Inst J. 2005.

Abstract

We describe a procedure to promote angiogenesis and impregnation of skeletal myoblast into infarcted myocardium. At the completion of coronary artery bypass surgery, the midline sternotomy incision was extended to open the abdomen, and the greater omentum was tailored to reach the myocardium. Four pieces of autologous rectus muscle were applied to the infarcted left ventricle. This implantation was reinforced by the greater omentum. Incisions were closed in the usual manner. Postoperatively, the patient showed significant improvements in left ventricular ejection fraction (from 0.15 to 0.40) and in exercise tolerance (from 3 METs to 6 METs, or 100%). Computed tomographic angiography and positron emission tomography demonstrated improved myocardial viability and vascularity in the ischemic segments of the left ventricle. Omentopexy and cell patch cardiomyoplasty in conjunction with coronary artery bypass surgery may stimulate myogenesis and angiogenesis in avascular, dyskinetic scar tissue of left ventricle; in this preliminary study, this procedure appeared to improve the functional capacity of the left ventricle.

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Figures

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Fig. 1 Polar maps of representative left anterior descending coronary artery ligation in the rabbit. Left and right panels are ammonia (NH3) and fluorodeoxyglucose (FDG) positron emission tomographic polar maps, respectively. Closely matched defects of perfusion and glucose metabolism are noted in the apex and in the distal anteroseptal wall, although the FDG defect is larger.
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Fig. 2 Ammonia (NH3) and fluorodeoxyglucose (FDG) polar maps of a representative cellular patch cardiomyoplasty (CEPAC) rabbit. Myoplasty was performed at the same surgical session as the left anterior descending coronary artery ligation. Note the protective effect of CEPAC on apex and anterior wall perfusion (FDG image) and metabolism (NH3 image).
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Fig. 3 Photomicrograph (H&E, orig. x 100) shows regeneration of transplanted skeletal muscle (black arrow) penetrating into infarcted myocardium. The white arrow depicts regenerated cardiac muscle.
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Fig. 4 Perfusion: The postoperative rubidium (Rb) study shows improvement in resting myocardial perfusion in the basal posterior wall, the inferior segment, and the basal septum, with persistently reduced perfusion at the apex. Metabolism: Postoperative viability study using fluorodeoxyglucose (FDG) demonstrates a moderate-size nontransmural infarct, which involves 15% of total left ventricular mass in the inferoapical and apicoseptal segments. There is improvement in FSG uptake in the inferobasal and apicolateral segments, the site of skeletal muscle grafting.
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Fig. 5 Computed tomographic angiogram shows new capillaries originating from the omentum and extending into the myocardium.

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