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Integrated Compensatory Responses in a Human Model of Hemorrhage
Published on: November 20, 2016
Physiological and hemodynamic evaluation of nonuniform direct cardiac compression
J H Artrip1, G H Yi, H R Levin
1Department of Surgery, Division of Cardiothoracic Surgery, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Biventricular direct cardiac compression (DCC) enhances heart function by improving ventricular pressure and increasing cardiac output. This novel approach avoids complications associated with blood-contacting ventricular assist devices.
Area of Science:
- Cardiovascular Physiology
- Biomedical Engineering
- Heart Failure Research
Background:
- Current ventricular assist devices pose risks due to blood/device interfaces.
- Biventricular direct cardiac compression (DCC) offers a bloodless alternative for cardiac support.
- A clinically designed DCC device was developed for synchronised cardiac compression.
Purpose of the Study:
- To evaluate the efficacy of a novel biventricular direct cardiac compression (DCC) device.
- To assess DCC's impact on cardiac function in failing heart models.
- To determine if DCC can mitigate complications of existing ventricular support systems.
Main Methods:
- Ex vivo canine heart preparation with a computerized afterload system.
- In vivo canine model of acute ischemic heart failure induced by coronary artery embolization.
- Testing DCC under various ventricular preloads and simulated heart failure conditions.
Main Results:
- DCC shifted the end-systolic pressure-volume relation upward by approximately 40% of compression pressure.
- In severe heart failure, DCC increased cardiac output (CO) by 104% and mean arterial pressure by 95%.
- CO was restored to about 60% of normal baseline values, demonstrating significant hemodynamic improvement.
Conclusions:
- Nonuniform DCC significantly enhances left and right ventricular pressure generation.
- DCC effectively increases cardiac output and mean arterial pressure in acute heart failure.
- DCC devices present a promising alternative, potentially avoiding blood/device interface complications.
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