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Published on: May 11, 2018
Development of DexAide right ventricular assist device: update II
Kiyotaka Fukamachi1, Diyar Saeed, Alex L Massiello
1Department of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
The DexAide right ventricular assist device (RVAD) shows promise for heart failure treatment. Successful 3-month in vivo tests and 18-month in vitro endurance testing were completed, paving the way for further development.
Area of Science:
- Cardiovascular Engineering
- Biomedical Devices
- Medical Technology
Background:
- The DexAide is a magnetically and hydrodynamically levitated implantable centrifugal pump designed as a right ventricular assist device (RVAD).
- Advancements in medical devices are crucial for managing end-stage heart failure.
Purpose of the Study:
- To report recent progress and ongoing development of the DexAide RVAD and a prototype biventricular assist device (BVAD) system.
- To evaluate the performance and reliability of the DexAide RVAD through in vitro and in vivo testing.
Main Methods:
- Redesign and testing of inflow/outflow conduits for the RVAD.
- Development and evaluation of alternative journal bearing materials.
- Completion of 18-month in vitro endurance testing of the RVAD.
- Acute and chronic implantation studies of the DexAide/CorAide BVAD system in calves, including those with induced heart failure.
Main Results:
- Two successful 3-month in vivo experiments with the redesigned RVAD conduits were completed.
- 18-month in vitro endurance testing of the RVAD was successfully finished.
- Acute BVAD implantations in calves demonstrated successful control algorithms and anatomical fit.
- Successful BVAD implantation in a calf with drug-induced chronic heart failure was achieved.
Conclusions:
- The DexAide RVAD has undergone significant development, including successful short-term in vivo and long-term in vitro testing.
- The development of a BVAD system shows potential for treating biventricular heart failure.
- Future steps include validating alternative bearing materials, conducting reliability studies, and seeking FDA approval for clinical trials.
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