coagulation disturbance Coagulopathy
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: * Coronary artery bypass graft (CABG), isolated and combined with aortic valve replacement (AVR) * Left ventricle ejection fraction > 35% * Age >18 years
Exclusion criteria
Exclusion criteria: * Any other procedure than CABG whether or not combined with AVR * Emergency surgery * History of bleeding diathesis or coagulopathy * Participation in any study involving an investigational drug or device * Inability to understand the study information and/or sign informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Several parameters will be studied in the collected blood samples, e.g.: Coagulation: - Aggregometer --> platelet aggregation - Prothrombin time, Activated partial thromboplastin time, fibrinogen, D-dimer - Platelets Fibrinolysis: Fibrinolytic assays (t-PA activity, PAI-I activity etc.) Thromboelastography, Fluorescence Activated Cell Sorter | — |
Secondary
| Measure | Time frame |
|---|---|
| Peroperative: - Operation time - CPB time - Aortic clamping time Postoperative: - Bloedtransfusions within 48 hours after surgery - Amount of blood loss within 48 hours after surgery - Total amount of blood loss after surgery | — |
Countries
Netherlands