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Published on: March 5, 2020
Cell adhesion and tissue factor upregulation in oxygenators used during coronary artery bypass grafting are modified
1Laboratory for Coagulation Research, Department of Medical Sciences, Clinical Chemistry, University Hospital, SE-751 85 Uppsala, Sweden.
Insights
A new heparin surface coating on cardiopulmonary bypass circuits reduces cell adhesion during coronary artery bypass grafting (CABG). Standard heparin levels with this coating are most biocompatible, preventing monocyte activation.
Area of Science:
- Biomedical Engineering
- Cardiovascular Surgery
- Hematology
Background:
- Cardiopulmonary bypass (CPB) can trigger inflammatory responses and coagulation activation.
- Cellular activation within oxygenators during CPB is a concern in coronary artery bypass grafting (CABG).
Purpose of the Study:
- To evaluate the impact of a novel heparin surface coating on oxygenator circuits.
- To assess cellular activation, specifically monocytes, within oxygenators during CABG.
Main Methods:
- Sixty patients undergoing CABG with CPB were randomized to uncoated or Corline Heparin Surface (CHS)-coated circuits.
- Three systemic heparin levels (standard, high, low) were tested.
- Adhered cells from oxygenators were analyzed for cell count, tissue factor (TF), and CD11b expression, and monocytic TF mRNA.
Main Results:
- The CHS coating effectively prevented granulocyte, monocyte, and platelet adhesion.
- Monocytes from oxygenators showed higher TF expression compared to circulating cells.
- Uncoated oxygenators had low TF expression but high TF mRNA; CHS with high heparin showed high TF expression and low TF mRNA.
Conclusions:
- The CHS coating demonstrated superior biocompatibility with standard heparin levels during CABG.
- Elevated systemic heparin levels, in conjunction with the CHS coating, paradoxically increased monocyte activation and TF upregulation.
Objective:
Cardiopulmonary bypass (CPB) is associated with inflammatory response and activation of coagulation. We investigated the influence of a new heparin surface on the activation of cells retrieved from oxygenators used during coronary artery bypass grafting (CABG).
Design:
Sixty patients undergoing CABG with CPB were randomly assigned to either uncoated or completely Corline Heparin Surface (CHS)-coated circuits with one of three different levels of systemic heparin: standard, high or low. At end of surgery adhered cells were retrieved from the oxygenators and cell count, tissue factor (TF)- and CD11b-expression on monocytes and monocytic TFmRNA were analysed.
Results:
The heparin coating of the oxygenator prevented adhesion of granulocytes, monocytes and platelets. TF-expression on monocytes from the oxygenators was significantly higher than on circulating cells in all groups. Monocytes from the uncoated oxygenators showed low levels of TF-expression with high levels of TFmRNA. The coated group with high level of heparin showed higher surface-expression of TF with low levels of TFmRNA.
Conclusion:
The CHS was most biocompatible with the standard level of heparin used during CABG whereas elevation of systemic heparin rather increased the activation and TF upregulation in monocytes from oxygenators.
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