This proposal intends to eliminate the two most important impediments of the artificial heart as a bridge to donor heart transplantation in human patients today. The space problem is eliminated by introducing small artificial hearts that fit easily inside the human chest. Thromboemboli are prevented by eliminating their origin - mechanical valves and quick connectors, while replacing them by tissue valves which are directly sewn into atria, aorta and pulmonary artery. The blood contacting surface of the hearts will be covered with Dacron fibrils to prevent possible small thrombi to become emboli. Durability and functional performance of these new ventricles will be studied in the mock circulation. A new, all pneumatic drive system with low dp/dt will be used to drive the hearts. Physiological studies will provide data for optimal use of this combination. Pyrolysis Mass Spectroscopy (Biomaterials Profiling Center) and other techniques of the University of Utah will guarantee quality of materials and detect degeneration after use. Five sheep or calves per year will receive the new hearts. Our hypothesis is that blood damage and coagulopathy will be minimal: kidneys will be free of emboli; calcification will not occur within three months in sheep; and function will be adequate on treadmill exercise. Two brain dead human cadavers per year will receive the new hearts at Temple University. This will demonstrate that implantation without quick connectors does not increase bleeding, and that there is an easy fit because of small ventricle size and absence of quick connectors. Compromising large veins and atria is thus prevented. Physiological studies will show by temporarily reducing or increasing CO of one ventricle that Starling's Law applies to the function of the other ventricle of the artificial heart. Tricusp semilunar Polyurethane valves are under development. If satisfactory, they will gradually replace the tissue valves. The ventricles will also be used as L-RVAD's in calves. When successful, a chimeric donor heart will be implanted with the assist pump in situ, thus allowing the donor heart to recover from damage it may have incurred. When the animal has not thrown any emboli and when we recover the artificial ventricles anyway, we might as well give the animal a chance.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL038304-03
Application #
3354492
Study Section
Surgery and Bioengineering Study Section (SB)
Project Start
1987-04-01
Project End
1991-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
3
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
Schools of Medicine
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Kolff, W J (1992) All is not well with the artificial heart. Artif Organs 16:118-22
Yu, L S; Versteeg, F; Kinoshita, M et al. (1990) Soft artificial ventricles for infants and adults, with or without a clamshell. ASAIO Trans 36:M238-42
Pijl, A J; Solen, K A; Mohammad, S F et al. (1990) Loss of anticoagulant effect of heparin during circulation of human blood in vitro. Artif Organs 14:125-9
Wijsmuller, E G; Yu, L S; Yuan, B et al. (1990) Development of a new inflow valve for a 20cc semisoft ventricle: preliminary results. Int J Artif Organs 13:503-8
Swier, P; Bos, W J; Mohammad, S F et al. (1989) An in vitro test model to study the performance and thrombogenicity of cardiovascular devices. ASAIO Trans 35:683-7
Yu, L S; Yuan, B; Bishop, D et al. (1989) New polyurethane valves in new soft artificial hearts. ASAIO Trans 35:301-4