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Updated: Jun 25, 2026

A Simplified Stepwise Approach to Echo Guidance during Percutaneous Mitral Valve Repair
Published on: October 16, 2021
HORIZONS trial: a step forward for primary percutaneous coronary intervention
1Green Lane Cardiovascular Service, Auckland City Hospital, Level 3, Building 32, Private Bag 92 024, Auckland 1030, New Zealand. harveyw@adhb.govt.nz
Insights
Bivalirudin significantly reduced bleeding and mortality in patients undergoing primary percutaneous coronary intervention (PCI). This antithrombotic agent demonstrated similar ischemic event rates compared to unfractionated heparin plus glycoprotein IIb/IIIa inhibitors.
Area of Science:
- Cardiology
- Pharmacology
- Interventional Cardiology
Background:
- Bivalirudin is an anticoagulant with a known association with reduced bleeding events.
- Existing data suggest similar ischemic event rates with bivalirudin across various acute coronary syndromes and elective percutaneous coronary intervention (PCI).
Purpose of the Study:
- To evaluate the efficacy and safety of bivalirudin compared to unfractionated heparin plus a glycoprotein IIb/IIIa inhibitor in patients undergoing primary PCI.
- To assess the impact of bivalirudin on bleeding events, mortality, and net clinical benefit.
Main Methods:
- The Harmonizing Outcomes with Revascularization and Stents in Acute Myocardial Infarction (HORIZONS-AMI) trial compared bivalirudin with unfractionated heparin plus a glycoprotein IIb/IIIa inhibitor during primary PCI.
- Outcomes assessed included major bleeding, death, reinfarction, target-vessel revascularization for ischemia, and stroke.
Main Results:
- Bivalirudin use resulted in a 40% reduction in major bleeding compared to the control group (4.9% vs. 8.3%).
- Net adverse clinical events were significantly reduced with bivalirudin (9.2% vs. 12.1%).
- Bivalirudin was associated with reduced cardiac and total mortality at both 30 days and 12 months post-procedure.
Conclusions:
- Bivalirudin is a safe and effective antithrombotic agent for patients undergoing primary PCI.
- It offers significant reductions in bleeding and mortality without compromising ischemic event rates.
- Bivalirudin represents an attractive therapeutic option in this patient population.
Abstract:
Bivalirudin has been associated with decreased bleeding, with similar rates of ischemia in patients with stable angina, unstable angina, non-ST elevation myocardial infarction and elective percutaneous coronary intervention (PCI). The Harmonizing Outcomes with Revascularization and Stents in Acute Myocardial Infarction trial tested whether with primary PCI, bivalirudin--compared with unfractionated heparin plus a glycoprotein IIb/IIIa inhibitor--reduced bleeding and net clinical benefit (bleeding, death, reinfarction, target-vessel revascularization for ischemia or stroke). Bivalirudin reduced major bleeding by 40% (4.9 vs 8.3%; risk ratio [RR]: 0.60; 95% confidence interval [CI]: 0.46-0.77; p < 0.0001) as compared with unfractionated heparin and a IIb/IIIa antagonist. Net adverse clinical events were reduced (9.2 vs 12.1%; RR: 0.76: 95% CI: 0.63-0.92; p = 0.005). Cardiac death and total death at 30 days were reduced with bivalirudin (1.8 vs 2.9%; p = 0.03) and (2.1 vs 3.1%; p = 0.047), and at 12 months (2.1 vs 3.8%; p < 0.005) and (3.4 vs 4.8%; p = 0.029), respectively. Bivalirudin reduced bleeding and net adverse clinical events as well as mortality compared with unfractionated heparin and a glycoprotein IIb/IIIa inhibitor. Bivalirudin is an attractive antithrombotic choice in patients undergoing primary PCI.
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