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Updated: Jul 9, 2026

Ferric Chloride-induced Murine Thrombosis Models
Published on: September 5, 2016
[Factor Xa-inhibition in interventional cardiology]
1Centre for Thrombosis & Myocardial Infarction, Baker Heart Research Institute, St Kilda Road Central, Melbourne, Victoria 8008, Australia. ingo.ahrens@baker.edu.au
Insights
Safer anticoagulants are needed for acute coronary syndromes (ACS) patients on antiplatelet therapy. Selective factor Xa inhibitors show promise for improving outcomes in ST-elevation myocardial infarction (STEMI) and other ACS cases.
Area of Science:
- Cardiology
- Pharmacology
- Hematology
Context:
- Bleeding events in acute coronary syndromes (ACS) patients correlate with poor clinical outcomes.
- Current anticoagulants (unfractionated heparin, low molecular weight heparins) have limitations.
- There is an unmet need for safer anticoagulants for patients on dual or triple antiplatelet therapy.
Purpose:
- To discuss the pharmacology of selective factor Xa inhibitors.
- To review indirect and direct selective factor Xa inhibitors.
- To explore their role in interventional cardiology for ACS patients.
Summary:
- Coagulation factors IIa and Xa are key targets for anticoagulants.
- New agents selectively inhibit factor Xa, offering potential safety benefits.
- Indirect selective factor Xa inhibitors (Fondaparinux, Idraparinux) and direct selective factor Xa inhibitors (DX-9065a, Otamixaban) are discussed.
Impact:
- Selective factor Xa inhibitors may offer improved safety profiles compared to traditional anticoagulants.
- These agents could enhance clinical outcomes for ACS patients, particularly those undergoing invasive procedures.
- Further research into selective factor Xa inhibitors is crucial for advancing anticoagulant therapy in cardiology.
Abstract:
The recently established correlation between bleeding events and clinical outcomes in patients with coronary artery disease undergoing either non-invasive or invasive treatment for acute coronary syndromes (ACS) highlights the unmet need for safer anticoagulants that can be used in conjunction with dual or triple antiplatelet therapy. The central position of the coagulation factors IIa and Xa within the coagulation system account for their prominent role as targets for anticoagulants. Unfractionated heparin (UFH) achieves a variable indirect inhibition of both factors. The low molecular weight heparins (LMWH) show favourable pharmacokinetics over UFH and have a more pronounced activity against factor Xa as opposed to thrombin which may partially account for the benefits observed with LMWH in clinical trials. New agents that have been developed allow for a selective inhibition of factor Xa. Recently, exciting results have been reported with an indirect selective inhibitor of factor Xa in patients with ST-elevation myocardial infarction (STEMI) -acute coronary syndromes (ACS) and non-STEMI-ACS. In this article the pharmacology of the indirect selective factor Xa inhibitors Fondaparinux and Idraparinux will be discussed along with the direct selective factor Xa inhibitors DX-9065a and Otamixaban in the setting of interventional cardiology.
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