Surgery: Cardiopulmonary bypass Surgery
Conditions
Interventions
Sponsors
Department of Health
Eligibility
Inclusion criteria
Inclusion criteria: Patients undergoing first-time, isolated, elective coronary artery bypass grafting at UHCW, who have not taken any anti-platelet medication for five days previous to the operation, will be eligible for the study. We aim to recruit 40 patients.
Exclusion criteria
Exclusion criteria: 1. Patients undergoing repeated surgery 2. Patients undergoing emergency surgery 3. Patients taking antiplatelet medication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post-operative blood loss and transfusion requirements, pulmonary, renal, neurological, cardiac and infective complications during hospitalisation, duration of ICU and hospital stay and thirty day mortality. The magnitude of the inflammatory response will be assessed by measuring plasma levels of inflammatory mediators. Platelet function and coagulation will be assessed by flow cytometry and thromboelastography. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed