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XARELTO®

(rivaroxaban)

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XARELTO - Reversal Agents in Human Studies - Other - Tranexamic Acid

Last updated : 05/16/2024

Clave et al (2012) assessed the efficacy of tranexamic acid in reducing blood loss during primary cementless THR in patients using XARELTO alone for thromboprophylaxis in a single-blind, prospective, case-control study.1

Study Design1

Study Assessments

  • To assess tranexamic acid action, pre- and postoperative blood effusion volume; real blood loss; need for PRBC transfusion; hemoglobinemia at day 0 (preoperative), day 1, and day 5; and complications were systematically collected.1
  • Twelve patients on antiplatelet therapy (6 in group A and 6 in group B) had therapy interrupted 5 days before surgery and resumed 1 day after surgery.1
  • In group A, no PRBC transfusions were needed; in group B, there were 4 transfusions.
  • No thromboembolic complications were observed at discharge or at 3-month follow-up.
  • Blood loss and mean hemoglobinemia between groups are provided in the table below.1

Blood Loss and Mean Hemoglobinemia1

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Group A: Tranexamic acid
(n=37)

Group B: Control
(n=33)

P-value

Mean peroperative blood effusion volume, mL

227.0

229.8

0.9529

Mean postoperative blood loss, mL

440.5

641.8

0.0002

Mean real blood loss, mL of 100% hematocrit

414.6

587.6

0.0006

Mean hemoglobinemia, g/dL

Day 0

14.15

14.14

0.471

Day 1

11.41

10.51

0.002

Day 5

11.05

10.24

0.002

IV, intravenous; PRBC, packed red blood cell; THR, total hip replacement.

Reference

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1. Clave A, Fazilleau F, Dumser D, et al. Efficacy of tranexamic acid on blood loss after primary cementless total hip replacement with rivaroxaban thromboprophylaxis: a case-control study in 70 patients. Orthop Traumatol Surg Res. 2012;98(5):484-490.