Antithrombogenicity evaluation of a centrifugal blood pump
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Updated: Oct 13, 2026

In Vitro Thrombosis Test for Ventricular Assist Devices
Published on: March 21, 2025
K Nakata1, M Yoshikawa, T Takano
1Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.
Insights
This study investigated thrombus formation in Gyro C1E3 pumps used as left ventricular assist devices (LVAD) and during percutaneous cardiopulmonary support (PCPS). A predictive equation was developed to estimate thrombus weight based on pump parameters and activated clotting time (ACT).
Area of Science:
- Biomedical Engineering
- Cardiovascular Devices
- Thrombosis Research
Background:
- The Gyro C1E3 pump is designed for cardiopulmonary bypass and short-term assist device applications.
- Understanding thrombus formation within these pumps is critical for patient safety and device efficacy.
Purpose of the Study:
- To investigate the correlation between thrombus formation factors and the Gyro C1E3 pump.
- To develop a predictive model for estimating thrombus accumulation within the device.
Main Methods:
- Seven Gyro C1E3 pumps were implanted in calves as paracorporeal left ventricular assist devices (LVAD) and one for percutaneous cardiopulmonary support (PCPS).
- Anticoagulation was managed with heparin to maintain specific activated clotting time (ACT) ranges.
- Post-experiment, pumps were examined for blood-derived deposits, and the dry weight of adhered thrombi was measured.
Main Results:
- A multiple correlation analysis was performed to identify factors influencing thrombus formation.
- An equation was derived to estimate thrombus dry weight based on pump flow rate, motor speed, pumping duration, and ACT: Estimated dry weight of thrombi = 1.140 x pump flow rate -0.001 motor speed + 1.652 pumping time -0.041 x ACT (R² = 0.944).
Conclusions:
- The study demonstrates a significant correlation between pump operational parameters and thrombus formation.
- The developed equation provides a method to quantify adhered thrombus formation within the Gyro C1E3 pump, aiding in risk assessment and device optimization.
Abstract:
The Gyro C1E3 pump was developed not only for cardiopulmonary bypass but also as a short-term assist device. The main purpose of this study was to examine the correlation between the thrombus formation factor and the Gyro C1E3 pumps. Seven pumps were implanted into 3 calves and evaluated for different periods of duration as a paracorporeal left ventricular assist device (LVAD). One pump was subjected to percutaneous cardiopulmonary support condition (PCPS) (total pressure head 500 mm Hg with a pump flow rate of 3 L/min). The anticoagulation treatment consisted of a continuous administration of heparin to maintain an activated clotting time (ACT) of 200-250 during the LVAD study and 250-300 during the PCPS study. After the experiment, the pumps were disassembled and examined. In cases where there were any blood-derived deposits inside the pumps, the dry weight of these thrombi that adhered to the bearing area of the pump was measured. A multiple correlation was attempted to speculate possible thrombus formation. The estimated dry weight of thrombi was calculated from pump flow rate, pumping day, motor speed, and activated clotting time. This equation was estimated dry weight of thrombi = 1.140 x pump flow rate -0.001 motor speed + 1.652 pumping time -0.041 x ACT + 2.198 R2 = 0.944. This study suggested that there was a possibility to calculate the amount of adhered thrombus formation from pump flow rate, motor speed, pumping day, and ACT.
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