This trial is being performed to evaluate the feasibility of the study protocol and to test the efficacy and safety of platelets stored at cold conditions (1-6°C) in 100% plasma for 10-14 days (CSP) in cardiac surgery patients who are actively bleeding and require platelet transfusion.
Cardiac surgery featuring cardiopulmonary bypass (CPB) has a detrimental effect on platelet function. Contact with foreign surfaces causes a transient platelet dysfunction. The bleeding time is prolonged for the time on bypass and reverts to normal approximately one hour after cardiac surgery in uncomplicated cases. Hemorrhage following cardiac surgery with CPB can cause surgical re-exploration and increased mortality. The overall risk for surgical re-exploration is between 2.5-5%. Patients who undergo re-exploration due to excessive bleeding have a 2-6 fold increased mortality compared with non-bleeding patients. Storage of platelets at 1-6°C has the advantage of potentially prolonging storage times while reducing bacterial contamination. Room-temperature storage has led to a 5 day storage time limit since bacterial growth and septic reactions increase rapidly after 5-7 days. CSP were the standard of care in the 1960-70s. CSP were abandoned when a reduced platelet survival was observed in platelet radiolabeling studies. Nevertheless, CSP may have several advantages over RSP in the study population including a state of pre-activation and therefore a potentially superior hemostatic function. A small pilot trial investigating CSP in cardiac surgery patients in Norway found a non-significant trend towards improved bleeding control with CSP transfusions. However, data evaluating the in vivo efficacy of CSP is limited in scale and quality with mixed results. The investigators and others have shown that CSP have a superior function compared with RSP in vitro and more data are needed to clarify the relative efficacy of CSP in vivo. The investigators hypothesize that 1) CSP are more effective than RSP at reducing blood loss and improving platelet function in subjects actively bleeding due to cardiac surgery with cardiopulmonary bypass (CPB), and that 2) CSP are safe and do not lead to increased risks relative to RSP.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
30
Subjects will receive cold stored platelets from the start of surgery until 24 hours after the end of surgery
Subjects will receive room temperature stored platelets from the start of surgery until 24 hours after the end of surgery
Swedish Medical Center - Cherry Hill
Seattle, Washington, United States
RECRUITINGFeasibility of the recruitment and accrual into the study protocol.
Number of subjects screened and enrolled into the study protocol.
Time frame: 24 hours following end of cardiac surgery
Total allogeneic blood units transfused (RBCs only, platelets only, plasma only, and composite of all three)
Number of units
Time frame: Start of surgery to 24 hours after surgery
Chest tube output volume
volume of chest tube output measured in milliliters.
Time frame: 24 hours after completion of surgery
Hemostatic agents administered
The total individual doses of hemostatic agents
Time frame: 24 hours after completion of surgery
Number of subjects requiring surgical re-exploration due to uncontrolled bleeding
binary
Time frame: 24 hours after completion of surgery
Number of subjects with evidence of new infection or sepsis
per protocol definition
Time frame: Through post-op day 3
Number of subjects with evidence of a thrombotic event
per protocol definition
Time frame: Through study completion, an average of 3 weeks.
Number of subjects with evidence of liver injury.
Maximum post-operative change from pre-surgical baseline within the first three days
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Time frame: Through post-op day 3
Hospital free days
Number of days out of the hospital.
Time frame: Post-op through day 28.
ICU free days
Number of days out of the ICU
Time frame: Post-op through day 28.
Ventilator free days
Number of days not on a ventilator.
Time frame: post-op through day 28.
Mortality
To evaluate mortality at 28 days.
Time frame: Post-op through day 28.