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Published on: February 28, 2012
Extended-release acetylsalicylic acid for secondary prevention of stroke and cardiovascular events
Kevin P Bliden1, Udaya S Tantry1, Rahul Chaudhary1
1a Inova Center for Thrombosis Research and Drug Development , Inova Heart and Vascular Institute , Fairfax , VA , USA.
Insights
Extended-release aspirin may offer an alternative to standard aspirin for secondary prevention of cardiovascular events, potentially mitigating bleeding risks. Further research is needed to confirm its safety and efficacy compared to traditional aspirin therapy.
Area of Science:
- Cardiology
- Pharmacology
- Neurology
Background:
- Aspirin is a cornerstone in secondary prevention of cardiovascular and cerebrovascular events.
- Standard aspirin therapy presents limitations including bleeding, gastrotoxicity, and short duration of effect.
- Extended-release (ER) aspirin formulations aim to address these limitations.
Purpose of the Study:
- To review the use of aspirin for secondary prevention of stroke and cardiovascular events.
- To describe pharmacodynamics of standard and extended-release aspirin formulations.
- To evaluate ER aspirin as a potential alternative to standard aspirin therapy.
Main Methods:
- Comprehensive literature search of PubMed articles until May 2016.
- Review of active- and placebo-controlled clinical trials.
- Analysis of American and European recommendations and controversies.
Main Results:
- Standard aspirin therapy increases bleeding risk with P2Y12 inhibitors or oral anticoagulants.
- Ongoing trials are evaluating low-dose oral anticoagulants as aspirin alternatives.
- ER aspirin may offer a safer alternative, but further studies are warranted.
Conclusions:
- ER aspirin formulations may provide an alternative to standard aspirin for secondary cardiovascular prevention.
- Further research is necessary to confirm the safety and efficacy of ER aspirin.
- Addressing safety concerns associated with standard aspirin therapy is crucial.
Introduction:
Aspirin has been the bedrock of antiplatelet treatment strategies for the secondary prevention of recurrent cardiovascular and cerebrovascular events for the last 3 decades. The limitations of standard aspirin therapy include bleeding, gastrotoxicity, and loss of antiplatelet effect over a 24-hour period in selected high-risk patients. An extended-release (ER) aspirin formulation, Durlaza® (New Haven Pharmaceuticals, Inc., North Haven, CT), has been developed to address some of the latter limitations and may provide an alternative to standard aspirin in the secondary prevention of cardiovascular disease.
Areas Covered:
We searched articles describing the use aspirin for secondary prevention of stroke and cardiovascular events in PubMed published until May 2016. This is a comprehensive review which describes active- and placebo-controlled clinical trials, overview of American and European recommendations, controversies surrounding standard aspirin use, and a description of pharmacodynamics of standard and extended release aspirin formulations. Expert commentary: Available data indicates an increased bleeding risk with the use of standard aspirin therapy in conjunction with potent P2Y12 receptor blockers, and/or oral anticoagulants. Trials evaluating the efficacy of replacing aspirin with a low-dose oral anticoagulant in patients with stable cardiovascular disease or acute coronary syndrome are ongoing. Future studies are warranted to determine if the use of ER-ASA formulation may obviate safety concerns surrounding standard aspirin therapy.
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