Korean J Thorac Cardiovasc Surg.
1999 Dec;32(12):1065-1077.
Animal Experiment of the Pneumatic Ventrivular Assist Device
- Affiliations
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- 1Department of Cardiovascular Surgery, Medical College, Dankook University.
- 2Department of Biomedical Engineering, Medical College, Dankook University.
- 3Department of Anesthesiology, Medical College, Dankook University.
- 4Department of Thoracic and Cardiovascular Surgery,
Seoul National University Hospital Seoul National University College of Medicine.
Abstract
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BACKGROUND: Ventricular assist devices(VADs) are being used for patients in postcvardiotomy
cardiogenic shock status bridge to cardiac transplant settings and in post-myocardial
infarction cardiogenic shock. The VAD which was developed at the Deparment of medical
engineering in Dankook University College of Medicine was a pneumatically driven device
and can maintain pulsatile flow. The goal of this study is to develop animal experimental
models using the VAD and to clarify the reliability and hemodynamic property adequacy of
end organ perfusion durability and severity of thrombotic-hemolytic tendency of the device.
MATERIAL AND METHOD: The pneumatic VAD was applied to 8 adult female lambs, We examined
some hemodynamic parameters such as arterial blood pressure pulmonary capillary wedge
pressure(pcwp) pulmonary artery pressure(PAP) left atrial pressure hour urine output
cardiac index VAD flow EKG to determine the reliability of the VAD and hemodynamic
compatibility of the experimental animals within 24 hours of experiment. We also observed
the end organ perfusion durability of the VAD and thrombotic-hemolytic property of the VAD
after 24 hours of VAD insertion.
RESULT: We could monitor all hemodynamic parameters including pcwp PAP cardiac index EKG,
adn hour urine as true clinical settings. We observed that the reliability of the VAD was
excellent and the hemodynamic property of the experimental animal and end organ perfusion
were adequate within 24 hours of experiment. In four lambs surviving 24 hours after insertion
the reliability of the VAD and end organ perfusion were excellent and no thrombotic-hemolytic
tendency was noted. However after 15 days of experiment the diaphragm of the VAD was torn and
it was recommende that the durability of the VAD should be extended.
CONCLUSION
e conclude that the pneumatic VAD developed at Dankook University Biomedical
Engineering has good hemodynamic property and low thromboembolic tendency and presents
adequate end organ perfusion but we noted that the durability of the device should be
expanded further. It will be possible to do more reliable experiment in the future according
to the animal experimental method developed in this study especially with the heart failure models.