Clinical Trial: Sequestration of Platelets Prior to Bypass Reduces Bleeding After Cardiac Surgery

Study Status: Terminated
Recruit Status: Terminated
Study Type: Interventional

Official Title: Post-operative Administration of Platelet Rich Plasma Sequestered Prior to Cardiopulmonary Bypass Reduces the Coagulopathy Associated With Complex Cardiac Surgery

Brief Summary: Excessive bleeding is common after cardiac surgery. This may result in patients receiving a blood transfusion or suffering the life-threatening complication of cardiac tamponade. Tamponade is when excessive bleeding compresses the heart and prevents it from pumping properly. A major reason for the bleeding is the damage done to platelets by the cardiopulmonary bypass (CPB) machine. Often patients receive platelets and plasma from blood donors to try to reduce the bleeding post-operatively. The investigators plan to take platelets and plasma from patients before they are damaged. They would then return these 'undamaged' sequestered platelets to the patients after the bypass machine is no longer needed. Therefore, the investigators' primary question is whether platelet sequestration would reduce the bleeding problems that occur following cardiac surgery. They will evaluate bleeding problems using thromboelastography, which provides a comprehensive assessment of both how blood clots form and their strength. If sequestration reduces bleeding problems following cardiac surgery then it may reduce the chance of patients receiving blood products from donors. Although donated blood is thoroughly tested, its use does expose patients to the risk of transfusion errors, blood borne infections and reactions. Avoiding its use would be very desirable.

Detailed Summary:

Hypothesis:

Patients undergoing repeat median sternotomy or requiring prolonged cardiopulmonary bypass (CPB) often develop a coagulopathy at the end of surgery. We propose sequestering plasma and platelets from these patients prior to CPB and thus prior to the dilution and platelet damage that occurs with CPB. We hypothesise that if these plasma and platelets are stored properly during CPB, and administered at the end of the operation, they will reduce any coagulopathy and the associated bleeding.

Study population:

Patients undergoing repeat median sternotomy, mitral valve repair, double valve operations, aortic surgery, or combined valve and coronary artery surgery.

Exclusion criteria will include those with anaemia, thrombocytopenia, unstable angina, anti-platelet therapy within the previous seven days, known or symptomatic cerebrovascular disease, known disorders of haemostasis, aprotinin sensitivity and pregnancy.

Intervention:

Patients will be randomised by a closed envelope technique to receive platelet/plasma sequestration or not. Patients randomised to undergo sequestration will have 14 mL/Kg blood taken. The blood will be separated into red cells and platelets/plasma. Anaemia would be prevented by returning the processed red blood cells to the patient. We will store platelets at 20-24°C/room temperature on a platelet rocker according to guidelines from the National Blood Service.

Assessment of coagulation:

Patients' coagulation status will be evaluated before and after surgery. Four methods will be employed to comp
Sponsor: Royal Brompton & Harefield NHS Foundation Trust

Current Primary Outcome: Incidence of coagulation abnormalities as assessed by thromboelastography and platelet function analyser [ Time Frame: At end of surgery (usually <1 day) ]

Original Primary Outcome: Incidence of coagulation abnormalities as assessed by thromboelastography and platelet function analyser

Current Secondary Outcome:

  • Volume of blood lost into chest drains during first 24 post-operative hours [ Time Frame: 24 hours ]
  • Volume of blood product administered during first 24 post-operative hours [ Time Frame: 24 hours ]
  • Length of stay in the intensive care unit (ICU) [ Time Frame: Usually < 30 days ]
  • ICU mortality [ Time Frame: Usually < 30 days ]
  • Incidence of surgical re-exploration [ Time Frame: Hospital admission (usually < 30 days) ]


Original Secondary Outcome:

  • Incidence of surgical re-exploration
  • Volume of blood lost into chest drains during first 24 post-operative hours
  • Volume of blood product administered during first 24 post-operative hours
  • Length of stay on the intensive care unit
  • ICU mortality


Information By: Royal Brompton & Harefield NHS Foundation Trust

Dates:
Date Received: August 1, 2006
Date Started: August 2006
Date Completion:
Last Updated: April 13, 2016
Last Verified: April 2016