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The clinical and economic impact of bivalirudin for percutaneous coronary intervention
Nikesh Malik1, Anthony H Gershlick
1Department of Cardiovascular Sciences, University Hospitals of Leicester NHS Trust, Glenfield Hospital, Groby Road, Leicester, LE3 9QP, UK.
Insights
Bivalirudin (BVR), a direct thrombin inhibitor, is effective and safe for acute coronary syndrome patients undergoing percutaneous coronary intervention. It offers reduced bleeding complications compared to heparin and glycoprotein IIb/IIIa inhibitors, proving cost-effective.
Area of Science:
- Cardiology
- Pharmacology
- Thrombosis Research
Background:
- Bivalirudin (BVR) is a direct thrombin inhibitor.
- It is used as an antithrombotic agent with aspirin and ADP-receptor blockers for acute coronary syndrome (ACS) patients undergoing percutaneous coronary intervention (PCI).
Purpose of the Study:
- To evaluate the efficacy and safety of BVR compared to heparin plus glycoprotein IIb/IIIa inhibitors in ACS patients undergoing PCI.
- To assess the cost-effectiveness of BVR in this patient population.
Main Methods:
- Review of randomized clinical trials comparing BVR to heparin plus glycoprotein IIb/IIIa inhibitors.
- Analysis of economic data regarding BVR versus heparin plus glycoprotein IIb/IIIa inhibitors.
Main Results:
- BVR demonstrated at least equivalent efficacy in reducing ischemic endpoints compared to heparin plus glycoprotein IIb/IIIa inhibitors.
- BVR consistently showed a lower rate of bleeding complications.
- Economic analyses indicated BVR is cost-effective.
Conclusions:
- Bivalirudin is a clinically effective and safe antithrombotic agent for ACS patients undergoing PCI.
- Its favorable bleeding profile and cost-effectiveness support its inclusion in clinical guidelines.
- Ongoing research is exploring BVR's role with newer oral antiplatelet agents.
Abstract:
Bivalirudin (BVR) is a direct thrombin inhibitor used as an adjunctive antithrombotic agent in combination with aspirin and an ADP-receptor blocker in patients with acute coronary syndrome undergoing percutaneous coronary intervention. When compared to a strategy of heparin plus a glycoprotein IIb/IIIa inhibitor, BVR has been shown in a number of randomized clinical trials to be at least as effective at reducing ischemic endpoints and to have a consistently lower rate of bleeding complications. In addition, various economic analyses have shown it to be cost-effective compared to heparin plus a glycoprotein IIb/IIIa inhibitor and this, coupled with its proven clinical efficacy, has led to the incorporation of BVR into both EU and US clinical guidelines. Previous studies with BVR have mostly assessed its use in patients treated with aspirin and clopidogrel and further studies are ongoing to determine its role in combination with newer, more potent oral antiplatelet agents.
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