The cost-effectiveness of rivaroxaban with or without aspirin in the COMPASS trial

Andre Lamy1,2,3,4, John Eikelboom1,5, Wesley Tong1,2

  • 1Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Insights

The combination of rivaroxaban and aspirin is highly cost-effective for preventing cardiovascular events in patients with stable coronary artery disease or peripheral artery disease. This strategy reduces healthcare costs and improves quality-adjusted life years in Canada, France, and Germany.

Area of Science:

  • Cardiovascular Medicine
  • Health Economics

Background:

  • The COMPASS trial showed rivaroxaban plus aspirin is superior to aspirin alone for preventing major adverse cardiovascular events in stable coronary artery disease (CAD) or peripheral artery disease (PAD).
  • Evaluating the cost-effectiveness of this strategy is crucial for clinical and policy decisions.

Purpose of the Study:

  • To assess the cost-effectiveness of rivaroxaban 2.5 mg twice daily (BID) plus aspirin 100 mg compared to aspirin 100 mg alone in patients from the COMPASS trial.

Main Methods:

  • An in-trial analysis was combined with a 33-year extrapolation using a two-state Markov model.
  • Country-specific healthcare costs were applied to patient-level data, calculating quality-adjusted life years (QALYs) and incremental cost-effectiveness ratios (ICERs).

Main Results:

  • The rivaroxaban plus aspirin group incurred higher total costs but gained 1.17 QALYs over a lifetime horizon.
  • ICERs were $3946/QALY in Canada, $9962/QALY in France, and $10,264/QALY in Germany.
  • Subgroup analyses revealed lower ICERs for patients with PAD and polyvascular disease.

Conclusions:

  • Rivaroxaban 2.5 mg BID plus aspirin reduces direct healthcare costs and is highly cost-effective in Canada, France, and Germany, even after considering drug acquisition costs.
  • This combination therapy represents a valuable strategy for managing cardiovascular risk in appropriate patient populations.
Abstract

Related Concept Videos

Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants01:18

Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants

Oral anticoagulants are vital tools in preventing and treating blood clotting disorders. This diverse class of medications can be categorized as vitamin K antagonists, exemplified by warfarin, and direct thrombin inhibitors (DTIs), such as dabigatran, as well as factor Xa inhibitors, including rivaroxaban.
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
1.3K
Anticoagulant Drugs: Low-Molecular-Weight Heparins01:30

Anticoagulant Drugs: Low-Molecular-Weight Heparins

Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
864
Venous Thrombosis III: Interprofessional Care01:29

Venous Thrombosis III: Interprofessional Care

Venous thrombosis requires effective prevention and treatment strategies to improve patient outcomes and reduce potential complications.Prevention StrategiesHealthcare providers must prioritize preventing venous thromboembolism (VTE) for all adult patients upon admission. Interventions depend on bleeding and thrombosis risk, medical history, current medications, diagnoses, planned procedures, and patient preferences. Patients on bed rest should change positions every two hours and, if not...
18
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors01:20

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors

Antiplatelet drugs emerge as frontline defenders against the insidious threat of thromboembolic diseases, where abnormal clots obstruct vital blood vessels. These drugs stand as bulwarks, inhibiting platelet aggregation and clot formation, thereby mitigating the risk of life-threatening conditions like myocardial infarction, coronary artery disease, and thrombotic strokes.
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
621
Coronary Artery Disease V: Interprofessional Care01:27

Coronary Artery Disease V: Interprofessional Care

Interprofessional care for coronary artery disease includes pharmacological therapy and revascularization procedures.Pharmacological therapy for Coronary Artery Disease (CAD) aims to manage symptoms, prevent complications, and improve patient outcomes through various classes of medications:Antiplatelet Agents:Aspirin and Clopidogrel: These medications inhibit platelet aggregation, preventing blood clots, which is crucial for avoiding heart attacks and strokes. Doctors often prescribe these...
24
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists01:23

Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists

Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
248