Anticoagulation in Atherosclerotic Disease
Samer Al Said1, Christoph Bode1, Daniel Duerschmied1
1Department of Cardiology and Angiology I, Heart Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Insights
Low-dose rivaroxaban combined with aspirin significantly reduced cardiovascular events and all-cause mortality in patients with atherosclerotic disease. This novel approach offers a new therapeutic option for high-risk individuals, despite a slight increase in gastrointestinal bleeding.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Thrombosis Research
Background:
- Atherothrombotic events are a major concern in arteriosclerotic diseases, leading to heart attack, stroke, and limb ischemia.
- Current prevention strategies for stable patients rely on antiplatelet agents like aspirin and clopidogrel, but recurrent ischemic events persist.
- Excessive thrombin generation contributes to ongoing cardiovascular risk despite antiplatelet therapy.
Purpose of the Study:
- To evaluate the efficacy and safety of low-dose anticoagulation with a factor Xa inhibitor in patients with stable coronary heart disease or peripheral arterial disease.
- To assess the impact of combining rivaroxaban with aspirin on cardiovascular outcomes and mortality.
Main Methods:
- The COMPASS study investigated the addition of low-dose rivaroxaban (2.5 mg twice daily) to long-term aspirin therapy.
- Participants had stable coronary heart disease or peripheral arterial disease.
- Outcomes were compared between the rivaroxaban-aspirin group and aspirin monotherapy.
Main Results:
- The combination of rivaroxaban and aspirin significantly reduced cardiovascular death, myocardial infarction, and stroke.
- All-cause mortality was reduced by a relative 18% in the treatment group.
- An increase in gastrointestinal bleeding was observed, but fatal or intracranial hemorrhages did not increase.
Conclusions:
- Low-dose anticoagulation with rivaroxaban in addition to aspirin represents a new therapeutic strategy for high-risk patients with atherosclerotic disease.
- This regimen offers significant benefits in preventing major adverse cardiovascular events and reducing overall mortality.
- Further research is needed to manage bleeding risks, potentially with proton pump inhibitors.
Abstract:
The prevention of atherothrombotic events is an essential therapeutic goal in the treatment of patients with arteriosclerotic diseases. After plaque rupture, a rapidly growing thrombus can lead to acute vascular occlusion and thus heart attack, stroke or limb ischaemia. The acute therapy combines anticoagulation and platelet inhibition. However, the only available therapy so far in the primary and secondary prevention of stable patients is the platelet inhibitors aspirin and clopidogrel. Despite the use of antiplatelet therapies, including aspirin and P2Y12-receptor antagonists, some patients with artery disease continue to experience recurrent cardiovascular ischaemic events due to excessive thrombin generation beyond the acute period. As a result, studies have tested non-vitamin K antagonist oral anticoagulants (NOACs), specifically the factor Xa inhibitors, either alone or in combination with antiplatelet therapy, in the management of arterial disease. For the first time, the COMPASS study investigated low-dose anticoagulation in stable coronary heart disease or peripheral arterial disease. The addition of 2 × 2.5 mg rivaroxaban to long-term aspirin therapy not only prevented cardiovascular death, myocardial infarction and stroke, but even reduced all-cause mortality by a relative 18% after a mean follow-up of 23 months. This benefit came at the expense of more gastrointestinal bleeding, which might be reduced by the addition of a proton pump inhibitor (investigations are ongoing). Interestingly, however, there was no increase in fatal or intracranial haemorrhages. Therefore, a new standard therapy for high-risk patients with atherosclerotic disease may become available in the near future.
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