Study Comparing Desirudin With Heparin to Prevent Vein Clots After Heart and Lung Surgery
Deep Venous Thrombosis
About this trial
This is an interventional prevention trial for Deep Venous Thrombosis focused on measuring Deep venous thrombosis, DVT, Heparin induced thrombocytopenia, HIT, Direct thrombin inhibitor
Eligibility Criteria
Inclusion Criteria: Patients who are scheduled for elective Cardiac or Thoracic Surgery. Age > 18 years of age. Exclusion Criteria: Patients with a clinical suspicion or a documented history of DVT/PE Patients who may require anticoagulation during the post-op period. (i.e. Patients with a history of A-fib, scheduled for a MAZE procedure or placement of a mechanical valve, or those on Coumadin/IV heparin preoperatively) Patients who have a history of HIT or if there is a suspicion of the patient having HIT pre-operatively. Documented allergy to heparin, desirudin, or lepirudin Patients with a history of coagulation disorder Platelet count< 100 X109 /dl Active bleeding Serum Creatinine ≥ 1.5 mg/dl or CrCl ≤ 30 ml/min Patients with a baseline coagulopathy (INR > 1.5 or aPTT > 45 sec) Patients with liver disease Pregnancy Patients who require ventricular assist devices before or after surgery
Sites / Locations
- Barnes-Jewish Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Heparin
Desirudin (Iprivask™)
Both groups of patients will receive study drug three times a day (TID) for DVT prophylaxis. The current TID schedule is 0900, 1300, and 2100. The patients who are randomized to the Heparin (standard of care) group will receive subcutaneous injections of heparin three times a day (0900, 1300 and 2100).
Both groups of patients will receive study drug three times a day (TID) for DVT prophylaxis. The current TID schedule is 0900, 1300, and 2100. Patients who are randomized to the desirudin (study) group will receive 15 mg of subcutaneous desirudin twice a day (at 0900 and 2100). These patients will also receive an injection of normal saline placebo at 1300 so that patients in both groups will receive three injections at the same time points.