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A Snapshot of Coagulopathy After Cardiopulmonary Bypass
Judith Höfer1, Dietmar Fries2, Cristina Solomon3
1Department of Anesthesiology and Critical Care Medicine, Medical University Innsbruck, Innsbruck, Austria.
Insights
Cardiac surgery with cardiopulmonary bypass (CPB) significantly alters patient coagulation, affecting fibrinogen and platelet function. Understanding these changes is crucial for developing better transfusion strategies to manage bleeding risks during CPB.
Area of Science:
- Cardiology
- Hematology
- Surgical Science
Background:
- Cardiopulmonary bypass (CPB) in cardiac surgery is linked to substantial blood loss, increased use of allogeneic blood products, and higher morbidity/mortality rates.
- Coagulopathy during CPB is complex, with inconsistent treatment protocols leading to variable bleeding management.
Purpose of the Study:
- To review available data on patient coagulation status post-CPB.
- To inform the development of standardized transfusion algorithms for managing bleeding during cardiac surgery.
Main Methods:
- A nonsystematic literature review was conducted.
- Coagulation parameters in patients undergoing CPB were identified and analyzed.
Main Results:
- Prothrombin time and activated partial thromboplastin time increased, but with significant variability, suggesting limited reliability for guiding therapy.
- Thrombin generation parameters showed changes, including increased lag time and decreased peak generation.
- Fibrinogen levels and platelet count/function were most affected, with significant decreases in plasma fibrinogen concentration, FIBTEM maximum clot firmness, and platelet count.
Conclusions:
- CPB significantly impacts coagulation, with notable reductions in fibrinogen and platelet function.
- Variability in reported coagulation changes highlights the need for further research.
- Standardized transfusion algorithms are needed to guide hemostatic therapy effectively post-CPB.
Abstract:
Cardiac surgery involving cardiopulmonary bypass (CPB) is often associated with important blood loss, allogeneic blood product usage, morbidity, and mortality. Coagulopathy during CPB is complex, and the current lack of uniformity for triggers and hemostatic agents has led to a wide variability in bleeding treatment. The aim of this review is to provide a simplified picture of the data available on patients' coagulation status at the end of CPB in order to provide relevant information for the development of tailored transfusion algorithms. A nonsystematic literature review was carried out to identify changes in coagulation parameters during CPB. Both prothrombin time and activated partial thromboplastin time increased during CPB, by a median of 33.3% and 17.9%, respectively. However, there was marked variability across the published studies, indicating these tests may be unreliable for guiding hemostatic therapy. Some thrombin generation (TG) parameters were affected, as indicated by a median increase in TG lag time of 55.0%, a decrease in TG peak of 17.5%, and only a slight decrease in endogenous thrombin potential of 7%. The most affected parameters were fibrinogen levels and platelet count/function. Both plasma fibrinogen concentration and FIBTEM maximum clot firmness decreased during CPB (median change of 36.4% and 33.3%, respectively) as did platelet count (44.5%) and platelet component (34.2%). This review provides initial information regarding changes in coagulation parameters during CPB but highlights the variability in the reported results. Further studies are warranted to guide physicians on the parameters most appropriate to guide hemostatic therapy.
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