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Published on: November 18, 2015
Flow simulation-based particle swarm optimization for developing improved hemolysis models
B Torner1, D Frank2, S Grundmann2
1Institute of Turbomachinery, University of Rostock, Rostock, Germany. benjamin.torner@uni-rostock.de.
This study optimizes numerical models for predicting blood trauma in medical devices. The new method improves existing hemolysis predictions but highlights limitations in current stress-based models.
Area of Science:
- Biomedical Engineering
- Computational Fluid Dynamics
- Medical Device Design
Background:
- Blood-contacting medical devices require high hemocompatibility.
- In-silico trials (flow simulations) are crucial for device optimization.
- Accurate prediction of blood trauma, like hemolysis, is essential but challenging with current numerical models.
Purpose of the Study:
- To propose a novel optimization strategy for improving existing numerical hemolysis models.
- To enhance the development of future hemolysis prediction models for medical devices.
- To investigate the reliability of stress-based hemolysis models.
Main Methods:
- Performed flow simulations for three turbulent blood flow test cases.
- Numerically predicted hemolysis using widely-applied stress-based models.
- Utilized multiple-objective particle swarm optimization (MOPSO) to correlate flow field stresses with measured hemolysis across over one million predictions.
Main Results:
- The proposed optimization approach demonstrated an improvement over existing hemolysis models.
- The study identified deficiencies and limitations inherent in current stress-based hemolysis prediction models.
- Results indicate areas for future research to enhance model reliability.
Conclusions:
- The novel optimization path offers a viable method for refining numerical hemolysis models.
- Further research is needed to address the identified limitations of stress-based models for more reliable hemocompatibility assessment.
- This work contributes to the development of safer and more effective blood-contacting medical devices.
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