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Ann Thorac Surg 1997;64:81-85
© 1997 The Society of Thoracic Surgeons


Original Articles: Cardiovascular

Cardiac Binding in Experimental Heart Failure

Mikhail Vaynblat, MD, Mario Chiavarelli, MD, PhD, Himansu R. Shah, MD, Geeta Ramdev, MD, Michelle Aron, RDCS, Zvi Zisbrod, MD, Joseph N. Cunningham, Jr, MD

Divisions of Cardiothoracic Surgery and Cardiology, State University of New York-Health Science Center at Brooklyn, Brooklyn, New York

Accepted for publication January 10, 1997.

Background. Cardiomyoplasty is a potential therapy for heart failure. Its benefits are attributed to systolic augmentation (dynamic cardiomyoplasty) and prevention of cardiac dilatation (static cardiomyoplasty). To evaluate the static component, we used an artificial membrane for cardiac binding in a canine model of heart failure.

Methods. Intracoronary doxorubicin was administered weekly for 4 weeks to induce heart failure in 10 dogs, each of which was assigned to one of two treatment groups: (1) no treatment, or (2) cardiac binding. Hemodynamic data were obtained at operation and at 7 weeks after operation. Echocardiography was performed weekly.

Results. Left ventricular end-diastolic pressure and diameter, and right ventricular end-diastolic diameter increased in group 1 (from 9.6 ± 6.1 to 19.6 ± 2.3 mm Hg, p = 0.009; from 3.9 ± 0.4 to 5 ± 0.3 cm, p = 0.0013; and from 1.6 ± 0.2 to 1.9 ± 0.3 cm, p = 0.0036, respectively). Ejection fraction fell in group 1 from 0.60 ± 0.10 to 0.40 ± 0.04 (p = 0.0009) and in group 2 from 0.56 ± 0.02 to 0.40 ± 0.04 (p = 0.0001), but the difference between groups was not significant.

Conclusion. Cardiac binding reduces the ventricular dilatation associated with heart failure without exacerbating left ventricular dysfunction.


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Invited Commentary
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Ann. Thorac. Surg. 1997 64: 85. [Extract] [Full Text]



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