Coronary disease, cardiac valve disease
Conditions
Interventions
None listed
Sponsors
Amsterdam UMC, VUmc location
Eligibility
Inclusion criteria
Inclusion criteria: • Informed consent • Patients undergoing elective cardiac surgery
Exclusion criteria
Exclusion criteria: • Emergency operations • Patients with previous heart surgery • Patients undergoing elective thoracic aortic surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| •To determine the changes in COP between different priming fluids during cardiac surgery with CPB | — |
Secondary
| Measure | Time frame |
|---|---|
| • Is the serum albumin level correlated with the level of COP during cardiac surgery with CPB? • Is the change of COP during cardiac surgery with CPB associated with a change in extravascular fluid shift (positive fluid balance, weight gain, mean arterial pressure)? • Is the change of COP during cardiac surgery with CPB associated with intravascular hemodilution (hemoglobin, hematocrit, blood product use)? • Is the change of COP during cardiac surgery with CPB associated with blood loss and hemostasis (platelet count, fibrinogen, use of coagulation factors concentrate)? | — |
Contacts
Public ContactAnne Beukers
Amsterdam UMC, VUmc location
Outcome results
None listed