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Hemocompatibility of a coaxial pump catheter for less invasive heart surgery
Xavier M Mueller1, Monique Augstburger, Yves Boone
1Clinic for Cardiovascular Surgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland. xavier.mueller@chuv.hospvd.ch
Insights
This study evaluated a novel right heart bypass minipump for off-pump coronary artery bypass (OPCAB) surgery. The device demonstrated excellent hemocompatibility, with minimal impact on blood cells during a 6-hour test.
Area of Science:
- Cardiovascular Surgery
- Biomedical Engineering
- Hematology
Background:
- Off-pump coronary artery bypass (OPCAB) surgery can lead to hemodynamic instability due to right ventricular dysfunction.
- Heart manipulation during OPCAB necessitates strategies to maintain cardiac function.
Purpose of the Study:
- To assess the hemocompatibility of a novel coaxial atrial cannula minipump designed for right heart bypass.
- To evaluate the safety and efficacy of this device during a 6-hour experimental run.
Main Methods:
- A minicentrifugal pump with a coaxial atrial cannula was tested in five calves for 6 hours at maximal speed (7000 rpm).
- Hemocompatibility was assessed through hourly blood sampling for blood gas, hematology, and chemistry analyses.
- Statistical analysis was performed using ANOVA.
Main Results:
- Hematocrit and red blood cell counts remained stable throughout the 6-hour experiment (p=0.77 and 0.87).
- Platelet counts showed no significant alteration (p=0.55), and LDH levels were stable (p=0.61).
- Plasma free hemoglobin stayed below 100 mg/l, indicating minimal red blood cell damage, and adequate tissue perfusion was maintained.
Conclusions:
- The developed right heart minipump demonstrates significant hemocompatibility with minimal impact on red blood cells and platelets.
- The system shows promise for enhancing hematological safety during OPCAB procedures requiring right heart support.
Abstract:
Off-pump coronary artery bypass (OPCAB) requires heart manipulation during exposure of the lateral and posterior walls of the heart, which may cause hemodynamic instability, mainly through right ventricular dysfunction. A coaxial atrial cannula connected to a minicentrifugal pump was developed to bypass the right heart. This study was designed to test the hemocompatibility of this pump ongoing for 6 h. In five calves (bodyweight, 70.3+/-4.2 kg), the pump was inserted and set to its maximal motor speed of 7000 rpm. Blood samples were taken for blood gas analyses, hematology and chemistry on an hourly basis. ANOVA was used for statistical analysis. During the 6-h run, hematocrit and red blood cell count were stable (p=0.77 and 0.87, respectively). Platelet count was not significantly altered (p=0.55). LDH was stable (p=0.61) and plasma free hemoglobin remained below 100 mg/l throughout the experiment. Adequate tissue perfusion was maintained as reflected by the stable mixed venous oxygen saturation (baseline, 72.5+/-2%, and 6 h, 65.6+/-3.4%) and no defect of any pump system was detected during this 6-h testing. This right heart minipump appears to have a minimal impact on red cells and platelets when set at its maximal speed for 6 h, underlining the hematological safety of the system.
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