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A design improvement strategy for axial blood pumps using computational fluid dynamics
G W Burgreen1, J F Antaki, B P Griffith
1Department of Surgery, University of Pittsburgh, PA 15219, USA.
Summary
Computational fluid dynamics (CFD) simulations improved a novel axial flow blood pump design, reducing harmful reverse flow and enhancing efficiency. This iterative numerical approach mitigated blood trauma and thrombogenesis risks before physical prototyping.
Area of Science:
- Biomedical Engineering
- Fluid Dynamics
- Computational Science
Background:
- Non-traditional axial flow pumps require advanced design methods.
- Computational Fluid Dynamics (CFD) offers significant advantages in early-stage concept development.
- Initial designs may exhibit undesirable flow features like reverse flow, impacting efficiency and biocompatibility.
Purpose of the Study:
- To numerically evolve the design of a novel axial flow blood pump using CFD.
- To mitigate undesirable flow features, specifically reverse flow.
- To improve hydrodynamic efficiency and reduce the potential for blood trauma and thrombogenesis.
Main Methods:
- Utilized Computational Fluid Dynamics (CFD) for numerical simulation.
- Created geometric models of blood-wetted surfaces for iterative design changes.
- Solved incompressible Navier-Stokes equations in rotating coordinates to analyze fluid flow.
- Employed an evolutionary sequence of four design generations.
Main Results:
- CFD analysis revealed large regions of reverse flow in the initial design.
- Iterative geometric modifications led to significant improvements in fluid dynamics.
- Marked enhancements in major fluid dynamic aspects were observed across the four design generations.
- Reduced reverse flow and improved flow characteristics were achieved.
Conclusions:
- CFD is a powerful tool for optimizing non-traditional axial flow pump designs.
- Iterative numerical design significantly mitigates undesirable flow features.
- The optimized axial flow pump design shows improved hydrodynamic performance and reduced biocompatibility risks.