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Lior Sasson
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J Thorac Cardiovasc Surg 2003;126:1875-1879
© 2003 The American Association for Thoracic Surgery


Cardiopulmonary support and physiology

Preoperative use of enoxaparin is not a risk factor for postoperative bleeding after coronary artery bypass surgery

Benjamin Medalion, MDa,*, George Frenkel, MDa, Paulina Patachenko, MDb, Eli Hauptman, MDa, Lior Sasson, MDa, Arie Schachner, MDa

a Department of Cardiothoracic Surgery, The Edith Wolfson Medical Center, Holon, Israel,
b Department of Hematology, The Edith Wolfson Medical Center, Holon, Israel

Received for publication January 7, 2003; revisions received May 18, 2003; accepted for publication June 17, 2003.

* Address for reprints: Benjamin Medalion, MD, Department of Cardiothoracic Surgery, The Edith Wolfson Medical Center, POB 5, Holon 58100, Israel
medalion{at}wolfson.health.gov.il

BACKGROUND: The purpose of this study was to determine whether the use of low-molecular-weight heparin before coronary artery bypass surgery would be associated with an increase in bleeding and use of blood products after the operation.

METHODS: Sixty-four patients (48 men and 16 women) aged 64 ± 10 years who were undergoing primary coronary artery bypass surgery were prospectively studied. Forty-one patients were treated with either subcutaneous enoxaparin 1 mg/kg twice daily (n = 21; enoxaparin group) or intravenous heparin (n = 20; heparin group). Patients received the last dose of enoxaparin 8.7 ± 0.75 hours (range, 8-10 hours) before skin incision. Heparin was stopped before transfer to the operating room. An additional 23 consecutive patients who received neither enoxaparin nor heparin served as controls (n = 23). Anti–factor Xa activity, a measure of enoxaparin and heparin activity, was measured at the start of the operation in all patients.

RESULTS: There was no perioperative mortality. The length of stay and frequency of postoperative complications were similar between groups. Preoperative anti–factor Xa activity was present only in the enoxaparin group (0.43 ± 0.25 IU/mL). Chest tube drainage at 24 hours was 553 ± 160 mL, 532 ± 140 mL, and 587 ± 230 mL for the enoxaparin, heparin, and control groups, respectively (P = .48). There was no difference among groups in the amount of blood products transfused.

CONCLUSIONS: Enoxaparin administration more than 8 hours before coronary artery bypass surgery is not associated with increased postoperative bleeding or blood product transfusion.





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