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Quantitation of platelet preservation with prostanoids during simulated bypass
The Journal of Surgical Research
|January 1, 1987
Summary
Cardiopulmonary bypass causes harmful platelet changes, increasing bleeding after heart surgery. Inhibiting platelet function with Iloprost (ZK) or PGE1 during bypass preserves platelet counts and function.
Area of Science:
- Cardiovascular Surgery
- Hematology
- Biomaterials Science
Background:
- Blood-synthetic surface interactions during cardiopulmonary bypass (CPB) lead to adverse platelet alterations.
- These alterations can increase blood loss following open cardiac surgery.
- Temporary inhibition of platelet function may mitigate these changes.
Purpose of the Study:
- To quantify platelet functional and structural alterations during simulated extracorporeal circulation (SEC).
- To compare the efficacy of Iloprost (ZK) and Prostaglandin E1 (PGE1) in inhibiting these alterations.
Main Methods:
- Fresh heparinized human blood was recirculated in a circuit with silicone rubber components and a membrane oxygenator for 2 hours.
- Simulated extracorporeal circulation (SEC) was performed with and without Iloprost (ZK) or PGE1.
- Platelet counts, mean platelet volume, and platelet aggregation responses to epinephrine and thrombin were measured.
Main Results:
- Uninhibited blood recirculation significantly decreased platelet counts and mean platelet volume, while increasing dispersion.
- Both Iloprost (ZK) and PGE1 significantly preserved platelet counts compared to no drug.
- Platelets recirculated with PGE1 showed reduced aggregation responses compared to those merely incubated with PGE1.
Conclusions:
- Platelet inhibition with Iloprost (ZK) or PGE1 during simulated extracorporeal circulation preserves platelet counts and reduces structural alterations.
- PGE1's effectiveness may be reduced by the extracorporeal circuit itself.
- Further optimization of platelet inhibition strategies is needed for CPB.