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Updated: Apr 21, 2026

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Insertion, Maintenance, and Removal of the Percutaneous Dual Lumen Cannula Right Ventricular Assist Device
Published on: July 20, 2022
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A novel less invasive single port pulsatile ventricular assist device
Li Li1, Jinsong Chen2, Zhongjiang Zhuang2
1Department of Surgery, University of Kentucky, Lexington, Kentucky.
JHLT Open
|April 20, 2026
Summary
A new less invasive paracorporeal single port pulsatile ventricular assist device (sppVAD) offers temporary left ventricle support for cardiogenic shock. This device demonstrated effective flow and stable hemodynamics in sheep with good short-term hemocompatibility.
Area of Science:
- Cardiovascular Engineering
- Medical Devices
- Hemodynamics
Background:
- Cardiogenic shock requires immediate circulatory support.
- Existing ventricular assist devices (VADs) can be invasive.
- Development of less invasive VADs is crucial.
Purpose of the Study:
- To develop and evaluate a less invasive paracorporeal single port pulsatile ventricular assist device (sppVAD).
- To assess the sppVAD's performance and hemocompatibility in a preclinical setting.
Main Methods:
- Fabrication of a sppVAD system including a valved single lumen cannula (VSLC) and a valveless single port diaphragm displacement pump (spDDP).
- Mock loop testing with a 33/27 Fr VSLC to evaluate flow capacity.
- In vivo testing in sheep (n=5) using a 28/25 Fr VSLC for 6-hour duration, assessing hemodynamic stability and hemocompatibility.
Main Results:
- The sppVAD achieved a flow of 6.2 L/min in mock loop testing.
- In sheep, the VSLC was implanted rapidly (within 1 minute) without cardiopulmonary bypass.
- The device provided 3.75 L/min flow in sheep with stable hemodynamics and unchanged hemocompatibility markers over 6 hours.
Conclusions:
- The less invasive sppVAD successfully provided total left ventricle support.
- The device demonstrated acceptable short-term hemocompatibility in a preclinical model.
- The sppVAD shows promise as a temporary VAD for managing cardiogenic shock.
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