Background Patients who undergo total hip replacement have ahigh risk of thromboembolic complications. Recombinant hirudin(desirudin), a specific inhibitor of thrombin, represents anew development in antithrombotic therapy. We compared the efficacyand safety of desirudin with those of a low-molecular-weightheparin (enoxaparin) for the prevention of thromboembolic complicationsin patients undergoing primary total hip replacement.
Methods Both treatments, which were assigned in a randomized,double-blind manner, were started preoperatively: enoxaparinon the evening before surgery, and desirudin within 30 minutesbefore the start of surgery. The dose of desirudin was 15 mgsubcutaneously twice daily, and the dose of enoxaparin was 40mg subcutaneously once daily. The duration of treatment was8 to 12 days. Deep-vein thrombosis was verified by bilateralvenography performed at the end of the treatment period or earlier,if there were clinical signs of deep-vein thrombosis.
Results At 31 centers in 10 European countries, 2079 eligiblepatients were randomly assigned to receive desirudin or enoxaparin.A total of 1587 patients were included in the primary analysisof efficacy. In the desirudin group, as compared with the enoxaparingroup, there was a significantly lower rate of proximal deep-veinthrombosis (4.5 vs. 7.5 percent, P = 0.01; relative reductionin risk, 40.3 percent) and a lower overall rate of deep-veinthrombosis (18.4 vs. 25.5 percent, P = 0.001; relative reductionin risk, 28.0 percent). The safety profiles were similar inthe two treatment groups.
Conclusions When administered 30 minutes before total hip replacement,desirudin is more effective than enoxaparin in preventing deep-veinthrombosis.
Source Information
From the Departments of Orthopedics and Radiology, SahlgrenskaÖstra University Hospital, Göteborg, Sweden (B.I.E., P.K.); the Center for Clinical Thrombosis Research, Bispebjerg Hospital, Copenhagen, Denmark (P.W.-J.); Orthopädische Klinik der Städtischen Klinik, Goethe Universität, Frankfurt am Main, Germany (P.M.); the Département d'AnesthésieRéanimation, Hôpital Cochin, Paris (N.R.); the Department of Orthopedic Surgery, Krankenhaus, Wiener Neustadt, Austria (P.B.); Novartis, Basel, Switzerland (M.B., S.E., D.B., P.C.); and Novartis, Stockholm, Sweden (S.L.).
Address reprint requests to Dr. Eriksson at the Department of Orthopedics, SahlgrenskaÖstra University Hospital, S-416 85 Göteborg, Sweden.
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