Key result
Rivaroxaban was associated with a significantly higher incidence of bleeding (1.2%) compared to warfarin or warfarin plus enoxaparin (0.4%) after major orthopedic surgery.
Why the study?
Does rivaroxaban increase bleeding or VTE events compared to warfarin or warfarin plus enoxaparin in patients after major orthopedic surgery?
Cohort (n=3,246)
No
Does rivaroxaban increase bleeding or VTE events compared to warfarin or warfarin plus enoxaparin in patients after major orthopedic surgery?
Effect estimate: IRR 0.218 (warfarin vs rivaroxaban) and IRR 0.242 (warfarin+enoxaparin vs rivaroxaban)
Absolute Event Rate: 1.2% vs 0.4%
p-value: p=0.0120 and 0.021
Rivaroxaban is associated with a small but significant increase in bleeding compared to warfarin-based regimens for VTE prophylaxis in the immediate postoperative period after major orthopedic surgery.
May favor warfarin-based regimens to minimize bleeding after major orthopedic surgery; leaves open net benefit pending randomized confirmation.
STUDY OBJECTIVES: To evaluate the occurrence of bleeding and venous thromboembolic (VTE) events in patients receiving rivaroxaban, warfarin, or warfarin with the addition of enoxaparin during the immediate postoperative period following major orthopedic surgery. METHODS: Patients older than 18 years who received at least one dose of rivaroxaban the morning following surgery, adjusted dose warfarin, or adjusted dose warfarin with the addition of enoxaparin for VTE prophylaxis after major orthopedic surgery between October 1, 2011, and February 28, 2015, were included. Data collected from the electronic health record included patient demographics, renal function, inpatient aspirin, P2Y12 inhibitor and/or nonsteroidal antiinflammatory drug (NSAID) use, type of surgery, postoperative analgesia, and presence of VTE risk factors. Adjusted incidence rate ratio for bleeding or VTE events was estimated using modified Poisson regression with robust standard errors. Covariates included in a multivariable model were age, sex, aspirin use, P2Y12 inhibitor use, NSAID use, obesity, VTE risk factors, and creatinine clearance. RESULTS: There were 3246 patients who met study inclusion criteria. Overall, incidences of bleeding and VTE events were rare. Bleeding event incidence ranged from 0.4% in the warfarin and warfarin with the addition of enoxaparin groups to 1.2% in the rivaroxaban group (p=0.088). There were two major bleeding events and 18 minor bleeding events (including hemorrhagic wound complications). VTE event incidence ranged from 0.2% in the warfarin with the addition of enoxaparin group to 0.6% in the rivaroxaban group (p=0.230). Two deep vein thromboses and 10 pulmonary emboli occurred. With use of the multivariable model, the warfarin and warfarin with the addition of enoxaparin groups had significantly lower incidence rates of bleeding compared with rivaroxaban (incidence rate ratio [IRR] = 0.218, p=0.0120, and IRR = 0.242, p=0.021, respectively). PRINCIPAL CONCLUSIONS: We observed a small, yet significant, increase in rivaroxaban-related bleeding in the immediate postoperative period relative to warfarin or warfarin with the addition of enoxaparin for the prevention of VTE after major orthopedic surgery.
No takes yet. Share an insight, caveat, or question.
Cieri et al. (2016) conducted a cohort in Major orthopedic surgery (n=3,246). Rivaroxaban vs. Warfarin or warfarin with enoxaparin was evaluated on Bleeding events (IRR 0.218 (warfarin vs rivaroxaban) and IRR 0.242 (warfarin+enoxaparin vs rivaroxaban), p=0.0120 and 0.021). Rivaroxaban was associated with a significantly higher incidence of bleeding (1.2%) compared to warfarin or warfarin plus enoxaparin (0.4%) after major orthopedic surgery.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: