4.8 Article

Aspirin or Rivaroxaban for VTE Prophylaxis after Hip or Knee Arthroplasty

Journal

NEW ENGLAND JOURNAL OF MEDICINE
Volume 378, Issue 8, Pages 699-707

Publisher

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa1712746

Keywords

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Funding

  1. Canadian Institutes of Health Research
  2. Bayer Pharma
  3. Bristol-Myers Squibb
  4. Pfizer
  5. Leo Pharma
  6. Boehringer Ingelheim
  7. Pendopharm
  8. Victhom
  9. Bodycad
  10. Sanofi
  11. Smith Nephew
  12. Stryker
  13. Ministere de la Sante et des Services Sociaux
  14. Bayer
  15. Octapharma
  16. Shionogi
  17. Bristol-Myers Squibb/Pfizer
  18. Alexion
  19. Portola
  20. McCarthy Tetrault
  21. Daiichi Sankyo
  22. DePuy Synthes
  23. Zimmer Biomet
  24. MicroPort
  25. Daiichi Sankyo Pharma
  26. Bayer Healthcare

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BACKGROUND Clinical trials and meta-analyses have suggested that aspirin may be effective for the prevention of venous thromboembolism (proximal deep-vein thrombosis or pulmonary embolism) after total hip or total knee arthroplasty, but comparisons with direct oral anticoagulants are lacking for prophylaxis beyond hospital discharge. METHODS We performed a multicenter, double-blind, randomized, controlled trial involving patients who were undergoing total hip or knee arthroplasty. All the patients received once-daily oral rivaroxaban (10 mg) until postoperative day 5 and then were randomly assigned to continue rivaroxaban or switch to aspirin (81 mg daily) for an additional 9 days after total knee arthroplasty or for 30 days after total hip arthroplasty. Patients were followed for 90 days for symptomatic venous thromboembolism (the primary effectiveness outcome) and bleeding complications, including major or clinically relevant nonmajor bleeding (the primary safety outcome). RESULTS A total of 3424 patients (1804 undergoing total hip arthroplasty and 1620 undergoing total knee arthroplasty) were enrolled in the trial. Venous thromboembolism occurred in 11 of 1707 patients (0.64%) in the aspirin group and in 12 of 1717 patients (0.70%) in the rivaroxaban group (difference, 0.06 percentage points; 95% confidence interval [CI], -0.55 to 0.66; P<0.001 for noninferiority and P=0.84 for superiority). Major bleeding complications occurred in 8 patients (0.47%) in the aspirin group and in 5 (0.29%) in the rivaroxaban group (difference, 0.18 percentage points; 95% CI, -0.65 to 0.29; P=0.42). Clinically important bleeding occurred in 22 patients (1.29%) in the aspirin group and in 17 (0.99%) in the rivaroxaban group (difference, 0.30 percentage points; 95% CI, -1.07 to 0.47; P=0.43). CONCLUSIONS Among patients who received 5 days of rivaroxaban prophylaxis after total hip or total knee arthroplasty, extended prophylaxis with aspirin was not significantly different from rivaroxaban in the prevention of symptomatic venous thromboembolism.

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