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The Journal of Thoracic and Cardiovascular Surgery, Vol 88, 11-21, Copyright © 1984 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
WF Bernhard, DG Gernes, WC Clay, FJ Schoen, R Burgeson, RC Valeri, AJ Melaragno and VL Poirier
A permanent, implantable, circulatory support system for patients with
irreversible cardiomyopathy is gradually becoming a reality. Progress has
been achieved toward formation of a stable, nonthrombogenic, blood-
prosthesis interface, and an electrically actuated ventricular assist
device has reached an advanced stage of fabrication. The two most important
components of the system, an electromechanical energy converter and a
contiguous, pusher-plate, blood pump (stroke volume 85 ml) were employed in
these studies. The energy converter consisted of a 50 volt, low-speed,
brushless, torque motor and a mechanism to convert rotary motion into a
pulsatile output. An electronic controller and variable-volume compliance
chamber were not evaluated. Left ventricular bypass experiments were
conducted in 13 calves for periods of 30 to 149 days. Preoperatively, four
devices were inoculated with bovine, fetal fibroblasts to accelerate
formation of a collagenous lining, and nine nonseeded pumps served as
controls. The collagen-lined devices functioned for longer periods of time
with unrestricted blood flow and no thromboembolic complications when
compared to the control devices. Additional studies are contemplated
employing a complete VAD system prior to undertaking preclinical trials.
ARTICLES
Investigations with an implantable, electrically actuated ventricular assist device
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