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Published on: May 26, 2023
[Antithrombotic therapy of acute myocardial infarction]
1Innere Medizin III (Kardiologie), Universitätsklinik Freiburg, Hugstetter Strasse 55, Freiburg, Germany. Martin.Moser@uniklinik-freiburg.de
Insights
Inhibition of blood coagulation is key for acute myocardial infarction treatment. Risk stratification guides anticoagulation intensity and invasive therapy timing for better patient outcomes.
Area of Science:
- Cardiology
- Pharmacology
Context:
- Acute myocardial infarction (AMI) management relies on inhibiting blood coagulation.
- Risk stratification is crucial for tailoring anticoagulation and invasive strategies.
Purpose:
- To outline current anticoagulation strategies for acute myocardial infarction based on patient risk and planned interventions.
Summary:
- All myocardial infarction patients require aspirin and clopidogrel.
- High-risk patients undergoing invasive therapy need immediate unfractionated heparin (or enoxaparin) plus a glycoprotein IIb/IIIa antagonist; bivalirudin is a potential alternative.
- Low-risk patients with delayed intervention may benefit from fondaparinux due to a lower bleeding risk, though unfractionated heparin is required for percutaneous coronary intervention.
Impact:
- Optimizing anticoagulation therapy based on risk stratification can improve patient outcomes in acute myocardial infarction.
- This approach allows for personalized treatment, balancing efficacy with bleeding risk.
Abstract:
Inhibition of blood coagulation is an essential cornerstone of the therapy of acute myocardial infarction. Risk stratification represents a valuable tool to adjust the intensity of anticoagulation and timing of invasive therapy according to patient risk. All patients presenting with myocardial infarction should be treated with aspirin and clopidogrel. Patients with ST-segment elevation myocardial infarction and high-risk patients with myocardial infarction without ST-segment elevation who undergo invasive therapy should be treated immediately with unfractionated heparin (alternatively enoxaparin) and a glycoprotein (GP) IIb/IIIa antagonist in the catheter laboratory. The direct thrombin antagonist bivalirudin may emerge as an attractive alternative in these patients. In low-risk patients who undergo delayed urgent elective interventional therapy the factor Xa antagonist fondaparinux may be advantageous because of its low bleeding rate. In these patients administration of unfractionated heparin is necessary for percutaneous coronary intervention.
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