Key result
Recent 2017 trials on antithrombotic drugs highlight the efficacy of low-dose anti-Xa with aspirin and the safety benefits of dual over triple antithrombotic therapy following coronary intervention.
Why the study?
What are the most recent clinical trial findings regarding antithrombotic drugs for cardiovascular diseases?
What are the most recent clinical trial findings regarding antithrombotic drugs for cardiovascular diseases?
This review highlights 2017 advancements in antithrombotic therapy, emphasizing a shift towards tailored regimens that balance ischemic efficacy with bleeding safety across various cardiovascular interventions.
PURPOSE OF REVIEW: To provide an up to date review of the most recent randomized clinical trials in the field of antithrombotic drugs for cardiovascular diseases. RECENT FINDINGS: In 2017, low-dose anti-Xa treatment added to aspirin proved to be more efficacious than either treatment alone in patients with stable atherosclerotic disease despite the increase in nonfatal bleeding events. Furthermore, anticoagulation strategy during coronary interventions was again tested in a registry-based trial and showed comparable efficacy and safety between heparin alone and bivalirudin. Data from safety trials demonstrated lower risk of bleeding with dual antithrombotic therapy compared with triple antithrombotic therapy following coronary intervention, albeit these trials were underpowered for efficacy. Although still in its infancy, the role of antithrombotic treatment following transcatheter aortic valve replacement (TAVR) has been investigated in small trials with evidence that a single antiplatelet drug may be noninferior to dual antiplatelet therapy with a better safety profile. SUMMARY: In this review, we discuss the most recent clinical trials investigating antithrombotic drugs for cardiovascular diseases published in 2017.
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Ibrahim et al. (2018) conducted a review in Cardiovascular diseases. Antithrombotic drugs was evaluated. Recent 2017 trials on antithrombotic drugs highlight the efficacy of low-dose anti-Xa with aspirin and the safety benefits of dual over triple antithrombotic therapy following coronary intervention.
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