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Published on: February 26, 2013
[Combined Antithrombotic Therapy in Patients with a Stable Atherosclerotic Cardiovascular Diseases: What Direction
1Kuban State Medical University, Ministry of Health of the Russian Federation, Krasnodar.
Insights
Adding low-dose rivaroxaban to aspirin significantly reduces cardiovascular death, heart attack, and stroke in patients with stable ischemic heart disease or peripheral artery disease. This combination therapy also lowers amputation risk in PAD patients without increasing fatal bleeding.
Area of Science:
- Cardiology
- Vascular Medicine
- Pharmacology
Background:
- Stable ischemic heart disease (IHD) and peripheral artery disease (PAD) patients face significant residual cardiovascular complication (CVC) risk despite current antiplatelet therapies.
- Atherothrombosis prevention strategies require further optimization, with coagulation pathways offering potential targets.
- Existing secondary prevention guidelines present challenges in practical application.
Purpose of the Study:
- To evaluate the efficacy and safety of adding rivaroxaban to aspirin for secondary prevention in patients with IHD and/or PAD.
- To assess the impact of combination antithrombotic therapy on cardiovascular outcomes and bleeding events.
- To identify patient subgroups who may benefit most from this intensified prevention strategy.
Main Methods:
- The study analyzed data from the COMPASS trial, comparing aspirin monotherapy to aspirin plus rivaroxaban (2.5 mg twice daily).
- Outcomes included major adverse cardiovascular events (MACE), all-cause death, and bleeding events (major, fatal, intracranial).
- Subgroup analyses focused on patients with specific risk profiles, including those with PAD and high CVC risk.
Main Results:
- Combination therapy with rivaroxaban and aspirin significantly reduced the risk of cardiovascular death, myocardial infarction, stroke, and all-cause death compared to aspirin alone.
- Major bleeding risk was increased with combination therapy, but fatal or intracranial bleeding did not significantly increase.
- Peripheral artery disease patients experienced a reduced risk of severe lower limb ischemic events, including amputations.
Conclusions:
- Adding low-dose rivaroxaban to aspirin provides superior secondary prevention for patients with stable atherosclerotic disease (IHD/PAD), significantly lowering CVC risk.
- The benefits of combination therapy, particularly in reducing ischemic limb events, outweigh the increased risk of major bleeding in high-risk patients.
- This strategy appears most beneficial for stable atherosclerotic patients at high risk for severe CVC, without a prohibitive increase in bleeding risk.
Abstract:
In patients with stable ischemic heart disease (IHD) and/or peripheral artery disease (PAD), current secondary prevention, including the antiplatelet monotherapy, is associated with a significant residual risk of recurrent cardiovascular complications (CVC). Practical application of results from many modern studies evaluating the effect of secondary prevention of atherothrombosis is complicated. An additional influence on coagulation may play a key role in prevention of atherothrombosis. In the COMPASS study, adding rivaroxaban 2.5 mg, b.i.d., to the acetylsalicylic acid (ASA) monotherapy significantly reduced the risk of death from cardiovascular complications, myocardial infarction or stroke, or all-cause death compared to the ASA monotherapy, in patients with IHD or PAD. The combination antithrombotic therapy was associated with an increased risk of major, but not fatal, or intracranial bleeding. In addition, PAD patients had a reduced risk of severe ischemic lower limb complications, including amputations. According to the subgroup analysis in the COMPASS study, supplementing ASA with rivaroxaban 2.5 mg, b.i.d., may appear most beneficial for patients with stable atherosclerotic disease and with a high risk of severe CVC without causing an increased risk of bleeding.
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