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Published on: May 28, 2019
Anticoagulation with bivalirudin during percutaneous coronary intervention for ST-segment elevation myocardial
Joseph F Stella1, Ronald E Stella, Robert A Iaffaldano
1Heart Care Centers of Illinois, Interventional Cardiology Division, 2338 New Street, Blue Island, IL, 60406, USA. jstella@heartcc.com
Insights
Bivalirudin, a direct thrombin inhibitor, was safely used for ST-segment elevation myocardial infarction (STEMI) patients undergoing percutaneous coronary intervention (PCI) without glycoprotein IIb/IIIa inhibitors. This approach demonstrated excellent blood flow and low complication rates, suggesting feasibility for further trials.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Percutaneous coronary intervention (PCI) is the primary treatment for ST-segment elevation myocardial infarction (STEMI).
- Bivalirudin has shown efficacy and safety in reducing bleeding events in non-STEMI PCI procedures compared to heparin with glycoprotein IIb/IIIa inhibitors.
- Limited data exists on bivalirudin use in STEMI patients undergoing primary PCI.
Purpose of the Study:
- To assess the safety and feasibility of using bivalirudin, a direct thrombin inhibitor (DTI), as a sole anticoagulant during primary PCI for STEMI.
- To evaluate outcomes without the routine addition of glycoprotein (GP) IIb/IIIa inhibitors in high-risk STEMI patients.
Main Methods:
- A retrospective analysis of 91 consecutive high-risk STEMI patients undergoing primary PCI.
- Bivalirudin was administered as a bolus (0.75 mg/kg) followed by an infusion (1.75 mg/kg/hr).
- Outcomes were monitored over a 30-day follow-up period.
Main Results:
- The study included high-risk patients (40% female, 30% diabetes, 21% prior MI, 18% cardiogenic shock).
- PCI involved balloons, stents, or both, with 41% receiving intra-aortic balloon pumps and 24% using closure devices.
- Excellent Thrombolysis In Myocardial Infarction (TIMI) flow was achieved without additional GP IIb/IIIa inhibitors.
Conclusions:
- Bivalirudin anticoagulation in STEMI patients undergoing primary PCI is feasible and safe.
- Low mortality and complication rates were observed, supporting the use of bivalirudin without GP IIb/IIIa inhibitors.
- Further large-scale controlled trials are warranted to confirm bivalirudin's effectiveness in this population.
Objective:
The objective of this retrospective analysis of high-risk patients treated with bivalirudin during primary percutaneous coronary intervention (PCI) for ST-segment elevation myocardial infarction (STEMI) was to evaluate the safety and feasibility of direct thrombin inhibitor (DTI) without concomitant glycoprotein (GP) IIb/IIIa inhibition.
Background:
Reperfusion by PCI is the treatment of choice for patients with STEMI. In patients with stable or unstable angina without ST-segment elevation undergoing PCI, bivalirudin was at least as effective as heparin plus GPIIb/IIIa inhibitors in reducing ischemic events and more effective in preventing bleeding. There are no published studies detailing the use of bivalirudin in patients with STEMI.
Methods:
From 09/02 to 05/03 at the Heart Care Centers of Illinois, Blue Island, Illinois. Ninety-one consecutive patients with STEMI underwent PCI with or without stent placement. Bivalirudin was administered as a bolus dose (0.75 mg/kg) followed by infusion (1.75 mg/kg/hr) for the duration of the procedure. Outcomes were recorded over a 30-day follow-up period.
Results:
Patients (n = 91) had several high-risk characteristics (40% female, 30% diabetes mellitus, 21% previous MI and 18% cardiogenic shock). PCI procedures utilized balloons, stents, or a combination of both. Intraaortic balloon pumps were used for 41% and closure devices for 24% of patients.
Conclusions:
This evaluation demonstrates excellent TIMI flow without the addition of GPIIb/IIIa inhibitors. The low mortality and complication rates suggest anticoagulation with bivalirudin in patients with STEMI undergoing PCI is feasible and warrants further study in larger controlled trials to evaluate the effectiveness of bivalirudin in this patient population.
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