W. Girsch et al., EXPERIMENTAL DEVELOPMENT OF AN ELECTRICALLY STIMULATED BIOLOGICAL SKELETAL-MUSCLE VENTRICLE FOR CHRONIC AORTIC COUNTERPULSATION, European journal of cardio-thoracic surgery, 13(1), 1998, pp. 78-83
Objective: The chronic shortage of donor organs for cardiac transplant
ation and the high costs for mechanical assist devices demand the deve
lopment of alternative cardiac assist devices for the treatment of sev
ere heart failure. Cardiac assistance by stimulated skeletal muscles i
s currently investigated as such a possible alternative. The goal of t
he presented study was to construct a newly designed biological skelet
al muscle ventricle and to evaluate its possible hemodynamic efficacy
in an acute sheep model. Methods: A total of 14 adult sheep were used
for acute experiments. The entire thoracic aorta including the aortic
root was excised from a donor sheep. An aorto-pericardial pouch condui
t (APPC) was created by enlarging the aortic circumference in its midd
le section with two strips of pericardium. This biological conduit was
anastomosed in parallel to the descending aorta of a recipient sheep,
using the aortic root as an inflow valve to the conduit. Stimulation
electrodes were applicated to the thoracodorsal nerve and the latissim
us dorsi muscle was detached from the trunk and wrapped around the pou
ch. EGG-triggered functional electrical stimulation was applied during
cardiac diastole to simulate aortic counterpulsation. Stimulation was
performed during various hemodynamic conditions. Results: A standardi
sed surgical procedure suitable for long term studies was established
during six experiments. An APPC, with 70-80 mm filling volume, was fou
nd to be of optimal size. In another eight experiments, hemodynamic me
asurements were performed. Under stable hemodynamic conditions the sti
mulation of the biological skeletal muscle ventricle induced a signifi
cant increase of mean arterial pressure by 14% and mean diastolic pres
sure by 26%. During pharmacologically induced periods of cardiac failu
re, the stimulation of the APPC increased mean arterial pressure by 13
% and mean diastolic pressure by 19%. In all eight experiments, the di
astolic peak pressure reached supra-systolic values during stimulation
. Conclusions: The results demonstrate the hemodynamic efficacy of thi
s newly designed biological skeletal muscle ventricle as an aortic cou
nterpulsation device. Chronic experiments using a preconditioned fatig
ue-resistant muscle will further help to evaluate its possible clinica
l significance. (C) 1998 Elsevier Science B.V.