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Randomized Controlled Trial Comparative Study Clinical Trial
A prospective, randomized study of cardiopulmonary bypass temperature and blood transfusion.
- P E Stensrud, G A Nuttall, M A de Castro, M D Abel, M H Ereth, W C Oliver, S C Bryant, and H V Schaff.
- Department of Anesthesiology, Mayo Clinic, Rochester, Minnesota 55905, USA. stensrud.paul@mayo.edu
- Ann. Thorac. Surg. 1999 Mar 1; 67 (3): 711-5.
BackgroundWe hypothesized that normothermic cardiopulmonary bypass (CPB) would be associated with decreased blood loss and allogeneic transfusion requirements relative to hypothermic CPB.MethodsAfter obtaining institutional review board approval and informed patient consent, we conducted a prospective, randomized study of 79 patients undergoing CPB for a primary cardiac operation at normothermic (37 degrees C) (n = 44) or hypothermic temperature (25 degrees C) (n = 35). Blood loss and transfusion requirements in the operating room and for the first 24 hours in the intensive care unit were determined. A paired t test and rank sum tests were used. A p value of less than 0.05 was considered significant.ResultsThe normothermic and hypothermic CPB groups did not differ in demographic variables, CPB or cross-clamp duration, heparin sodium or protamine sulfate dose, prothrombin time, or thromboelastogram results. There were no differences between the two CPB groups in blood loss or transfusion requirements.ConclusionsWe found that when there was no difference in duration of CPB, normothermic and hypothermic CPB groups demonstrated similar blood loss and transfusion requirements even though other studies have shown hypothermia induces platelet dysfunction and alters the activity of the coagulation cascade.
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