Skeletal muscle ventricles are constructed from canine latissimus dors
i muscle. These skeletal muscle ventricles can be placed subcutaneousl
y on the chest wall or inside the chest cavity. Skeletal muscle ventri
cles are connected to the descending thoracic aorta and activated to p
ump blood as aortic diastolic counterpulsators. The skeletal muscle ve
ntricle in 1 animal pumped blood in the circulation for 27 months. Ske
letal muscle ventricles can also function effectively under the condit
ion of low cardiac output. Although thrombus has been detected in some
skeletal muscle ventricles, thromboembolism to distal organs has been
detected only rarely during the past few years. This research appears
promising; however, skeletal muscle ventricle rupture remains a probl
em and currently accounts for about 30% of the mortality in the long-t
erm experiments. It occurs at the site between the skeletal muscle ven
tricle outlet and the Dacron sewing ring that is necessary to connect
conduits from the skeletal muscle ventricle to the animal's circulatio
n. We believe that skeletal muscle ventricle rupture is likely to be a
solvable problem. Once a solution has been found, skeletal muscle ven
tricles may be read for clinical use in patients with chronic congesti
ve heart failure.