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Clopidogrel: a review of its use in the prevention of thrombosis
Greg L Plosker1, Katherine A Lyseng-Williamson
1Wolters Kluwer Health | Adis, Auckland, New Zealand, an editorial office of Wolters Kluwer Health, Conshohocken, Pennsylvania, USA. demail@adis.co.nz
Insights
Clopidogrel is an effective antiplatelet medication that reduces cardiovascular events, especially when added to aspirin therapy for acute coronary syndromes. It is a well-tolerated option for secondary prevention in various cardiovascular conditions.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Clopidogrel selectively and irreversibly inhibits adenosine diphosphate (ADP)-induced platelet aggregation.
- Established cardiovascular disease patients showed a modest advantage of clopidogrel over aspirin in reducing adverse cardiovascular outcomes (CAPRIE trial).
- Addition of clopidogrel to aspirin improved outcomes in acute coronary syndromes (CURE, COMMIT, CLARITY-TIMI 28 trials).
Purpose of the Study:
- To evaluate the efficacy and tolerability of clopidogrel as an antiplatelet agent.
- To assess clopidogrel's role in secondary prevention of ischemic events.
- To review unresolved issues regarding clopidogrel use, such as optimal dosing and treatment duration post-PCI and stent placement.
Main Methods:
- Analysis of results from large randomized trials including CAPRIE, CURE, COMMIT, and CLARITY-TIMI 28.
- Review of clinical data on clopidogrel's impact on cardiovascular outcomes.
- Examination of treatment guidelines from US and European bodies.
Main Results:
- Clopidogrel demonstrated a statistically significant advantage over aspirin in reducing adverse cardiovascular outcomes in established cardiovascular disease.
- Addition of clopidogrel to aspirin therapy significantly improved outcomes in patients with acute coronary syndromes.
- Clopidogrel is established as an effective and well-tolerated agent for secondary prevention in ischemic stroke and acute coronary syndromes.
Conclusions:
- Clopidogrel is a crucial antiplatelet agent for secondary prevention in patients with cardiovascular conditions.
- Current evidence supports clopidogrel's efficacy and tolerability in managing cardiovascular risks.
- Further research may be needed to address optimal dosing and duration for specific interventions like percutaneous coronary interventions (PCI).
Abstract:
Clopidogrel (Plavix), Iscover) selectively and irreversibly inhibits adenosine diphosphate (ADP)-induced platelet aggregation. Long-term administration of clopidogrel was associated with a modest but statistically significant advantage over aspirin in reducing adverse cardiovascular outcomes in patients with established cardiovascular disease in the CAPRIE trial. In other large well designed multicentre trials, such as CURE, COMMIT and CLARITY-TIMI 28, the addition of clopidogrel to aspirin therapy improved outcomes in patients with acute coronary syndromes. However, some issues regarding the use of clopidogrel remain unresolved, such as the optimal loading dose in patients undergoing percutaneous coronary interventions (PCI) and the optimal treatment duration following drug-eluting intracoronary stent placement. Results of several large randomised trials, therefore, have established clopidogrel as an effective and well tolerated antiplatelet agent for the secondary prevention of ischaemic events in patients with various cardiovascular conditions, including those with ischaemic stroke or acute coronary syndromes. In addition, treatment guidelines from the US and Europe acknowledge the importance of clopidogrel in contemporary cardiovascular medicine.
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