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Rivaroxaban versus enoxaparin for thromboprophylaxis after total knee arthroplasty

Lassen, Michael R (author)
Nordsjællands Hospital
Ageno, Walter (author)
University of Insubria
Borris, Lars C (author)
Aarhus University Hospital
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Lieberman, Jay R (author)
University of Connecticut
Rosencher, Nadia (author)
Cochin Hospital
Bandel, Tiemo J (author)
Bayer Corporation, USA
Misselwitz, Frank (author)
Bayer Corporation, USA
Turpie, Alexander G G (author)
McMaster University
Levine, M (creator_code:cre_t)
Flondell, M. (creator_code:cre_t)
Lund University,Lunds universitet,Medicinska fakulteten,Faculty of Medicine
Wykman, A (creator_code:cre_t)
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 (creator_code:org_t)
 
2008
2008
English.
In: The New England journal of medicine. - 0028-4793. ; 358:26, s. 86-2776
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: We investigated the efficacy of rivaroxaban, an orally active direct factor Xa inhibitor, in preventing venous thrombosis after total knee arthroplasty.METHODS: In this randomized, double-blind trial, 2531 patients who were to undergo total knee arthroplasty received either oral rivaroxaban, 10 mg once daily, beginning 6 to 8 hours after surgery, or subcutaneous enoxaparin, 40 mg once daily, beginning 12 hours before surgery. The primary efficacy outcome was the composite of any deep-vein thrombosis, nonfatal pulmonary embolism, or death from any cause within 13 to 17 days after surgery. Secondary efficacy outcomes included major venous thromboembolism (i.e., proximal deep-vein thrombosis, nonfatal pulmonary embolism, or death related to venous thromboembolism) and symptomatic venous thromboembolism. The primary safety outcome was major bleeding.RESULTS: The primary efficacy outcome occurred in 79 of 824 patients (9.6%) who received rivaroxaban and in 166 of 878 (18.9%) who received enoxaparin (absolute risk reduction, 9.2%; 95% confidence interval [CI], 5.9 to 12.4; P<0.001). Major venous thromboembolism occurred in 9 of 908 patients (1.0%) given rivaroxaban and 24 of 925 (2.6%) given enoxaparin (absolute risk reduction, 1.6%; 95% CI, 0.4 to 2.8; P=0.01). Symptomatic events occurred less frequently with rivaroxaban than with enoxaparin (P=0.005). Major bleeding occurred in 0.6% of patients in the rivaroxaban group and 0.5% of patients in the enoxaparin group. The incidence of drug-related adverse events, mainly gastrointestinal, was 12.0% in the rivaroxaban group and 13.0% in the enoxaparin group.CONCLUSIONS: Rivaroxaban was superior to enoxaparin for thromboprophylaxis after total knee arthroplasty, with similar rates of bleeding. (ClinicalTrials.gov number, NCT00361894.)

Subject headings

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

Keyword

Adult
Aged
Aged, 80 and over
Anticoagulants/adverse effects
Arthroplasty, Replacement, Knee
Double-Blind Method
Enoxaparin/adverse effects
Factor Xa Inhibitors
Female
Humans
Male
Middle Aged
Morpholines/adverse effects
Pulmonary Embolism/epidemiology
Rivaroxaban
Thiophenes/adverse effects
Venous Thromboembolism/epidemiology
Venous Thrombosis/epidemiology

Publication and Content Type

art (subject category)
ref (subject category)

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