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A once-daily, oral, direct Factor Xa inhibitor, rivaroxaban (BAY 59-7939), for thromboprophylaxis after total hip replacement

Eriksson, Bengt I., 1946 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Borris, L. C. (author)
Dahl, O. E. (author)
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Haas, S. (author)
Huisman, M. V. (author)
Kakkar, A. K. (author)
Muehlhofer, E. (author)
Dierig, C. (author)
Misselwitz, F. (author)
Kalebo, P. (author)
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 (creator_code:org_t)
2006
2006
English.
In: Circulation. - 1524-4539. ; 114:22, s. 2374-81
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Rivaroxaban (BAY 59-7939)--an oral, direct Factor Xa inhibitor--could be an alternative to heparins and warfarin for the prevention and treatment of thromboembolic disorders. METHODS AND RESULTS: This randomized, double-blind, double-dummy, active-comparator-controlled, multinational, dose-ranging study assessed the efficacy and safety of once-daily rivaroxaban relative to enoxaparin for prevention of venous thromboembolism in patients undergoing elective total hip replacement. Patients (n=873) were randomized to once-daily oral rivaroxaban doses of 5, 10, 20, 30, or 40 mg (initiated 6 to 8 hours after surgery) or a once-daily subcutaneous enoxaparin dose of 40 mg (given the evening before and > or = 6 hours after surgery). Study drugs were continued for an additional 5 to 9 days; mandatory bilateral venography was performed the following day. The primary end point (composite of any deep vein thrombosis, objectively confirmed pulmonary embolism, and all-cause mortality) was observed in 14.9%, 10.6%, 8.5%, 13.5%, 6.4%, and 25.2% of patients receiving 5, 10, 20, 30, and 40 mg rivaroxaban, and 40 mg enoxaparin, respectively (n=618, per-protocol population). No significant dose-response relationship was found for efficacy (P=0.0852). Major postoperative bleeding was observed in 2.3%, 0.7%, 4.3%, 4.9%, 5.1%, and 1.9% of patients receiving 5, 10, 20, 30, and 40 mg rivaroxaban, and 40 mg enoxaparin, respectively (n=845, safety population), representing a significant dose-response relationship (P=0.0391). CONCLUSIONS: Rivaroxaban showed efficacy and safety similar to enoxaparin for thromboprophylaxis after total hip replacement, with the convenience of once-daily oral dosing and without the need for coagulation monitoring. When both efficacy and safety are considered, these results suggest that 10 mg rivaroxaban once daily should be investigated in phase III studies.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)

Keyword

Administration
Oral
Adult
Anticoagulants/administration & dosage/*therapeutic use
*Arthroplasty
Replacement
Hip/mortality
Double-Blind Method
Drug Administration Schedule
Factor Xa/*antagonists & inhibitors
Female
Hemorrhage/*prevention & control
Humans
Male
Middle Aged
Morpholines/administration & dosage/*therapeutic use
Postmenopause
Postoperative Complications/*prevention & control
Safety
Sample Size
Survival Analysis
Thiophenes/administration & dosage/*therapeutic use

Publication and Content Type

ref (subject category)
art (subject category)

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