Related Experiment Video
Updated: Jul 16, 2026

Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Bivalirudin in percutaneous coronary intervention
1Department of Medicine, Flinders University, South Australia, Australia.
Insights
Bivalirudin, a direct thrombin inhibitor, offers a safe and effective alternative to heparin for patients undergoing percutaneous coronary intervention (PCI) and acute coronary syndrome (ACS), reducing bleeding without compromising efficacy.
Area of Science:
- Cardiovascular Pharmacology
- Thrombosis and Hemostasis
Background:
- Bivalirudin is a direct thrombin inhibitor anticoagulant.
- It is evaluated as an alternative to heparins in percutaneous coronary intervention (PCI) and acute coronary syndrome (ACS).
Purpose of the Study:
- Review the pharmacology of bivalirudin.
- Examine clinical trial evidence for its use in PCI and ACS.
Main Methods:
- Review of pharmacology of bivalirudin.
- Analysis of clinical trial data and meta-analyses in ACS and PCI settings.
- Discussion of early results from the ACUITY trial.
Main Results:
- Bivalirudin is a viable alternative to heparin plus glycoprotein IIb/IIIa inhibitors in PCI and ACS.
- Consistent reduction in bleeding rates without loss of anti-thrombotic efficacy across trials.
- Potential economic benefits due to reduced use of glycoprotein IIb/IIIa inhibitors.
Conclusions:
- Bivalirudin demonstrates pharmacokinetic and pharmacodynamic advantages over indirect anticoagulants.
- Clinical trials support bivalirudin as an effective and safe anticoagulant option.
- Further data from trials like ACUITY contribute to understanding its role in cardiovascular interventions.
Abstract:
Bivalirudin is a member of the direct thrombin inhibitor group of anticoagulants. It has been evaluated as an alternative to unfractionated and low-molecular-weight heparins in the settings of percutaneous coronary intervention (PCI) and acute coronary syndrome (ACS). Results of clinical trials to date suggest bivalirudin is a viable alternative to the use of a heparin combined with a glycoprotein (GP) IIb/IIIa inhibitor in these settings. Thrombin has a central role in coagulation and platelet activation in ACS and during PCI. Its direct inhibition is an attractive target for therapy in these settings. Bivalirudin is a 20 amino acid polypeptide hirudin analog. It displays bivalent and reversible binding to the thrombin molecule, inhibiting its action. Direct inhibition of thrombin with bivalirudin has theoretical pharmacokinetic and pharmacodynamic advantages over the indirect anticoagulants. A reduction in rates of bleeding without loss of anti-thrombotic efficacy has been a consistent finding across multiple clinical trials. There may be economic benefits to the use ofbivalirudin if it permits a lower rate of use of the GP IIb/IIIa inhibitors. This article reviews the pharmacology of bivalirudin and clinical trial evidence to date. There are now data from multiple clinical trials and meta-analyses in the setting of ACS and PCI. Early results from the acute catheterization and urgent intervention strategy (ACUITY) trial are discussed.
Related Concept Videos
Venous Thrombosis III: Interprofessional Care
Peripheral Artery Disease III: Interprofessional Care
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Pulmonary Embolism II: Diagnostic Studies and Interprofessional Care
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...