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Right arrow Cardiothoracic Anesthesia, Respiration and Airway
Canadian Journal of Anesthesia 47:255-260 (2000)
© Canadian Anesthesiologists' Society, 2000

Clinical Report

Recombinant hirudin anticoagulation for aortic valve replacement in heparin-induced thrombocytopenia

Dan Longrois, MD PhD*, Emmanuel de Maistre, MD{dagger}, Nicolas Bischoff, MD{ddagger}, Christian Dopff, MD*, Claude Meistelman, MD*, Michaël Angioï, MD§ and Thomas Lecompte, MD{dagger}

* From the Department of Anesthesia and Intensive Care, Department of Hematology,
{dagger} Haemostasis Unit, Department of Cardiovascular Surgery and
{ddagger} Department of Cardiology,
§ CHU Nancy-Brabois, Vandoeuvre-les-Nancy, France.

Address correspondence to: Dan Longrois MD PhD, Department of Anesthesia and Intensive Care, CHU Nancy- Brabois, 4, rue du Morvan 54500 Vandoeuvre les Nancy, France. Phone: 33-3-83-15-41-66; Fax: 33-3-83-15-36-88; E-mail: d.longrois{at}chu-nancy.fr

Purpose: To report the case of a patient with HIT that received a prolonged infusion of r-hirudin (lepirudin; Refludan®; Hoechst, France) before, during and after cardiopulmonary bypass (CPB) for aortic surgery. Although administration of r-hirudin for CPB anticoagulation has previously been reported, many questions persist concerning the best therapeutic regimen for CPB anticoagulation as well as the time of onset and the doses for postoperative anticoagulation.

Clinical Features: A 65-yr-old man was admitted for surgery of aortic stenosis after an episode of acute pulmonary edema complicated by deep venous thrombosis in the context of documented HIT. The patient received r-hirudin for 13 dy before surgery at doses (0.4 mg•kg–1 bolus followed by 0.15 mg•kg–1•hr–1 continuous infusion) that maintained activated partial thromboplastin time (aPTT) ratios between 2 and 2.5. Anticoagulation for CPB was performed with r-hirudin given as 0.1 mg•kg–1 iv bolus and 0.2 mg•kg–1 in the CPB priming volume. Anticoagulation during CPB was monitored with the whole blood activated coagulation time and ecarin clotting time (ECT) performed in the operating room with values corresponding to r-hirudin concentrations > 5 µg•ml–1 during CPB. Anticoagulation during CPB was uneventful. Two bleeding episodes, related to the r-hirudin regimen and necessitating allogeneic blood transfusion, occurred after surgery.

Conclusion: This case report confirms previous experience of the use of r-hirudin for anticoagulation during CPB and provides additional information in the context of prolonged r-hirudin infusion before and after CPB.




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