Rivaroxaban plus aspirin versus acenocoumarol to manage recurrent venous thromboembolic events despite systemic anticoagulation with rivaroxaban

Thromb Res. 2023 Feb:222:43-48. doi: 10.1016/j.thromres.2022.12.008. Epub 2022 Dec 21.

Abstract

Introduction: The evaluation and management of patients who sustain recurrent thromboembolic events while taking therapeutic anticoagulation have not been well characterized; moreover, there has been no systematic review or randomized trial focused on treating patients with recurrent deep vein thrombosis (DVT) and pulmonary embolism (PE) during anticoagulant treatment. Therefore, we developed a pilot trial to compare rivaroxaban plus aspirin versus acenocoumarol in patients with recurrent venous thromboembolism despite ongoing anticoagulation with rivaroxaban.

Materials and methods: The study was a multicenter, randomized clinical trial. We randomly assigned patients with objectively documented recurrent venous thromboembolism to receive rivaroxaban (20 mg once a day) plus aspirin (300 mg once a day) or an adjusted dose of acenocoumarol. The study was designed to evaluate the incidence of recurrent thromboembolic events (recurrent ipsilateral or contralateral DVT, PE, ischemic stroke, and myocardial infarction) and hemorrhagic events.

Results: A total of 58 patients were randomized: 28 were allocated to the rivaroxaban plus aspirin group and 30 to the acenocoumarol group. After 90 days of follow-up, three recurrent thromboembolic events (primary outcome) occurred in the acenocoumarol group - two DVTs and one ischemic stroke - and zero events in the rivaroxaban plus aspirin group (risk ratio [RR] 0.15; 95 % confidence interval [CI] 0.008-2.83; P = 0.20). Minor bleeding occurred in five patients in the acenocoumarol group and zero in the rivaroxaban plus aspirin group (RR 0.09; 95 % CI 0.005-1.68; p = 0.10). There was one non-fatal gastrointestinal major bleed in the rivaroxaban plus aspirin group.

Conclusions: In this pilot study, there were no significant differences in any outcome assessed; however, recurrent thromboembolic events and minor bleeding events occurred numerically less frequently in the rivaroxaban plus aspirin group. These data suggest the need to carry out more extensive randomized studies with sufficient statistical power to clarify these results.

Keywords: Acenocoumarol; Aspirin; Deep vein thrombosis; Pulmonary embolism; Recurrent venous thromboembolism; Rivaroxaban.

Publication types

  • Randomized Controlled Trial
  • Multicenter Study

MeSH terms

  • Acenocoumarol / adverse effects
  • Anticoagulants / therapeutic use
  • Aspirin / therapeutic use
  • Hemorrhage / chemically induced
  • Hemorrhage / drug therapy
  • Humans
  • Ischemic Stroke*
  • Pilot Projects
  • Pulmonary Embolism* / drug therapy
  • Rivaroxaban / pharmacology
  • Rivaroxaban / therapeutic use
  • Venous Thromboembolism* / drug therapy
  • Venous Thrombosis* / drug therapy

Substances

  • Rivaroxaban
  • Aspirin
  • Acenocoumarol
  • Anticoagulants