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Particles released from the Gyro C1E3 during simulated extracorporeal circulation
T Takano1, K Nakata, S Schulte-Eistrup
1Department of Surgery, Baylor College of Medicine, Houston, Texas 77030, USA. ttakano@bcm.tmc.edu
Artificial Organs
|July 13, 2000
Summary
The Gyro C1E3 centrifugal blood pump significantly reduces microembolism risk. It released fewer and smaller particles compared to a roller pump during simulated extracorporeal circulation.
Area of Science:
- Biomedical Engineering
- Medical Devices
- Cardiovascular Technology
Background:
- Microembolism is a risk during extracorporeal circulation.
- Released particles from blood pumps can cause microembolism.
- Evaluating particle release is crucial for blood pump safety.
Purpose of the Study:
- To evaluate particle release from the Gyro C1E3 centrifugal blood pump.
- To compare particle release between the Gyro C1E3 and a roller pump.
- To assess the risk of microembolism associated with the Gyro C1E3.
Main Methods:
- The Gyro C1E3 was operated for 14 days simulating left ventricular assist device (LVAD) and percutaneous cardiopulmonary support (PCPS).
- A roller pump was operated for 2 days for comparison.
- Released particles were collected, weighed, and analyzed using Scanning Electron Microscopy (SEM).
Main Results:
- After 14 days, the Gyro C1E3 released 238.6 microg of particles under LVAD conditions.
- The roller pump released 270.2 microg of particles in just 2 days.
- Average particle size was 0.6 microm for the C1E3 versus 3.7 microm for the roller pump.
Conclusions:
- The Gyro C1E3 demonstrates a substantially lower risk of microembolism due to reduced particle release.
- The centrifugal design of the Gyro C1E3 appears advantageous in minimizing particle generation.
- Further evaluation supports the Gyro C1E3 as a safer option for extracorporeal circulation support.