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Cardiopulmonary Bypass in a Mouse Model: A Novel Approach
Published on: September 22, 2017
Hemoadsorption does not Have Influence on Hemolysis During Cardiopulmonary Bypass
Martin H Bernardi1, Harald Rinoesl2, Robin Ristl3
1From the Division of Cardiac Thoracic Vascular Anesthesia and Intensive Care Medicine, Medical University of Vienna, Vienna, Austria.
This study found no significant reduction in hemolysis markers like free hemoglobin during cardiopulmonary bypass (CPB) when using a novel hemoadsorption device. However, some secondary markers suggested a potential moderate effect, warranting further investigation in larger trials.
Area of Science:
- Cardiovascular Surgery
- Hemostasis and Thrombosis
- Biomaterials and Medical Devices
Background:
- Cardiopulmonary bypass (CPB) is associated with hemolysis, leading to elevated plasma free hemoglobin.
- Hemolysis during CPB can contribute to postoperative complications.
- Novel hemoadsorption devices aim to mitigate adverse effects during CPB.
Purpose of the Study:
- To investigate the effect of a novel hemoadsorption device on hemolysis during CPB.
- To analyze changes in plasma free hemoglobin, haptoglobin, lactate dehydrogenase, and bilirubin levels.
- To evaluate the efficacy of hemoadsorption in reducing CPB-induced hemolysis.
Main Methods:
- Post hoc analysis of a single-center, blinded, controlled study.
- Inclusion of 35 patients undergoing elective CPB surgery with expected CPB duration > 120 minutes.
- Comparison between a hemoadsorption intervention group (n=17) and a control group (n=18).
Main Results:
- No significant difference in postoperative free hemoglobin levels between groups.
- Statistically significant differences in median haptoglobin levels (58.4 vs. 17.9 mg/dL; P < 0.01) on postoperative day 1.
- Significant differences in median lactate dehydrogenase levels (353.0 vs. 432.0 U/L; P < 0.05) on postoperative day 1.
Conclusions:
- The hemoadsorption device did not demonstrate a significant effect on reducing hemolysis markers during CPB in this study.
- Lower haptoglobin and higher secondary hemolysis markers in the control group suggest a potential moderate effect of the device.
- Larger studies are required to confirm the clinical significance of the observed differences.
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