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Updated: Apr 8, 2026

Postconditioning with Lactate-enriched Blood for Cardioprotection in ST-segment Elevation Myocardial Infarction
Published on: May 28, 2019
Antithrombotic therapy before, during and after emergency angioplasty for ST elevation myocardial infarction
Stefano Savonitto1, Giuseppe De Luca2, Patrick Goldstein3
11 Ospedale A. Manzoni, Lecco, Italy.
Insights
Timely intervention within three hours of symptom onset is crucial for ST-elevation myocardial infarction (STEMI) patients. Treatment strategies, including percutaneous coronary intervention and antithrombotic therapy, should be individualized based on patient risk and presentation time.
Area of Science:
- Cardiology
- Interventional Cardiology
- Thrombosis Research
Background:
- The initial three hours post-symptom onset are critical for myocardial salvage in ST-elevation myocardial infarction (STEMI).
- Early reperfusion strategies like primary percutaneous coronary intervention (PPCI) or pre-hospital fibrinolysis/glycoprotein IIb/IIIa-inhibitors (GPI) can restore coronary patency.
- Oral antiplatelet therapy may not provide sufficient platelet inhibition early on, and benefits diminish after the initial golden period.
Purpose of the Study:
- To review optimal antithrombotic treatment strategies for STEMI patients undergoing primary angioplasty.
- To discuss tailoring antithrombotic therapy based on coronary thrombotic burden, vascular approach, and bleeding risk.
- To highlight remaining challenges in STEMI management, including high-risk patients and dual antiplatelet therapy duration.
Main Methods:
- Review of current evidence and guidelines for antithrombotic therapy in STEMI.
- Analysis of treatment approaches based on patient presentation time and risk factors.
- Discussion of specific antithrombotic agents (GPI, bivalirudin, P2Y12 inhibitors) and their indications.
Main Results:
- A GPI-based approach may benefit early presenters with high thrombus burden, while bivalirudin without GPI suits higher bleeding risk patients.
- Oral P2Y12 inhibitors (prasugrel, ticagrelor) effectively prevent stent thrombosis and recurrent ischemic events post-PPCI.
- No data supports GPI use in bailout situations.
Conclusions:
- Antithrombotic treatment during primary angioplasty requires individualized tailoring based on clinical factors.
- Effective strategies exist for STEMI reperfusion, but challenges remain in managing high-risk bleeding patients and optimizing dual antiplatelet therapy duration.
- Further research is needed to address open issues in STEMI management.
Abstract:
The first three hours after symptom onset hold the maximum potential for myocardial reperfusion and salvage in ST-elevation myocardial infarction (STEMI) patients. During this period timely primary percutaneous coronary intervention (PPCI) or, when PPCI is not promptly feasible, pre-hospital administration of fibrinolyis or a glycoprotein IIb/IIIa-inhibitor (GPI) have been shown to restore coronary patency and reperfusion and even result in myocardial infarction (MI) abortion. On the other hand, oral antiplatelet therapy may not yet guarantee sufficient platelet inhibition. Patients presenting after this golden time have less, if any, benefit from an aggressive antithrombotic treatment prior to PPCI. Antithrombotic treatment during primary angioplasty should be tailored on the basis of the coronary thrombotic burden, vascular approach and the patient's risk of bleeding complications. A GPI-based approach may be favourable in patients presenting early with large MI and high thrombus burden, whereas a bivalirudin-based approach without GPI may be preferred in patients with higher bleeding risk. There are no data to support the use of GPI in bailout conditions. The powerful oral P2Y12 inhibitors, prasugrel and ticagrelor, have been clearly shown to prevent stent thrombosis and recurrent ischaemic events after emergency percutaneous coronary intervention in STEMI patients. Open issues remaining are the treatment of patients with high bleeding risk, such as the elderly and those requiring anticoagulation, as well as the duration of dual antiplatelet therapy after STEMI.
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