4.6 Article

Low-dose rivaroxaban and aspirin among patients with peripheral artery disease: a meta-analysis of the COMPASS and VOYAGER trials

Journal

EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY
Volume 29, Issue 5, Pages E181-E189

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/eurjpc/zwab128

Keywords

Rivaroxaban; Peripheral artery disease; Meta-analysis

Funding

  1. Bayer AG (COMPASS)
  2. Janssen Research & Development, LLC (VOYAGER)
  3. Tier 1 Canada Research Chair in Ethnicity and Cardiovascular Disease
  4. Michael G. DeGroote Heart and Stroke Foundation Chair in Population Health
  5. Jack Hirsh Population Health Research Institute Chair in Thrombosis Research
  6. Heart & Stroke Foundation/Marion W. Burke Chair in Cardiovascular Disease
  7. William R. Hiatt Chair in Cardiovascular Research

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Among peripheral artery disease (PAD) patients, low-dose rivaroxaban plus aspirin is superior to aspirin alone in reducing cardiovascular and limb events, including acute limb ischemia and major vascular amputation. Despite an increased risk of major bleeding, there is no significant increase in severe bleeding with the combination therapy.
Aims Peripheral artery disease (PAD) patients suffer a high risk of major cardiovascular (CV) events, with athero-thrombo-embolism as the underlying pathophysiologic mechanism. Recently, two large randomized clinical trials evaluated the efficacy and safety of low-dose rivaroxaban twice daily plus aspirin in stable PAD outpatients and those immediately after peripheral revascularization. We sought to determine if the effects of low-dose rivaroxaban and aspirin compared to aspirin alone are consistent across this broad spectrum of PAD patients. Methods and results We conducted a random-effects meta-analysis of the COMPASS and VOYAGER randomized trials among 11 560 PAD patients (4996 from COMPASS and 6564 from VOYAGER) in the primary analysis and 9332 (2768 from COMPASS and 6564 from VOYAGER) with lower extremity (LE)-PAD in the secondary analysis. The hazard ratio (HR) for the composite of CV death, myocardial infarction, ischaemic stroke, acute limb ischaemia, or major vascular amputation was 0.79 (95% confidence interval, CI: 0.65-0.95) comparing low-dose rivaroxaban plus aspirin to aspirin alone. While the risk of major bleeding was increased with low-dose rivaroxaban plus aspirin compared to aspirin alone [HR: 1.51 (95% CI: 1.22-1.87)], there was no significant increase in severe bleeding [HR: 1.18 (95% CI: 0.79-1.76)]. Similar effects were observed in the subset with symptomatic LE-PAD. Conclusions Among PAD patients, low-dose rivaroxaban plus aspirin is superior to aspirin alone in reducing CV and limb outcomes including acute limb ischaemia and major vascular amputation. This reduction is offset by a relative increase in major bleeding, but not by an excess of fatal or critical organ bleeding. The consistency of findings of these trials supports the use of combination low-dose rivaroxaban plus aspirin in PAD patients across a broad spectrum of disease.

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