Pokroky v antitrombotickej liecbe--antitrombotiká s anti-Xa ucinkom
[Advances in antithrombotic treatment--antithrombotics with anti-Xa effect]
Language Slovak Country Czech Republic Media print
Document type Journal Article, Review
PubMed
19378862
- MeSH
- Anticoagulants therapeutic use MeSH
- Fondaparinux MeSH
- Factor Xa Inhibitors * MeSH
- Humans MeSH
- Morpholines therapeutic use MeSH
- Polysaccharides therapeutic use MeSH
- Rivaroxaban MeSH
- Thiophenes therapeutic use MeSH
- Thromboembolism drug therapy prevention & control MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Anticoagulants MeSH
- Fondaparinux MeSH
- Factor Xa Inhibitors * MeSH
- Morpholines MeSH
- Polysaccharides MeSH
- Rivaroxaban MeSH
- Thiophenes MeSH
The use of anticoagulants in the prophylaxis and treatment of arterial and venous thrombosis has substantially expanded during the last years. Increasing knowledge about the inherited and acquired thrombophilia and the risk factors predisposing to the recurrency of thromboembolic events result in a new indications for primary and secondary thromboprophylaxis with prolonged or even life-long duration. The limitations of classical anticoagulans, heparin and vitamin K antagonists support the development of medicaments with a specific antithrombotic action. The new generation anticoagulants inhibit in a specific way either particular coagulation enzyme or hemostasis activation step. Based on the in vitro studies and extensive clinical observations the activated factor Xa (FXa) seems to be one of the most advantageous targets for a specific action of perspective antithrombotic agents. Two selective F Xa inhibitors have been approved for clinical use: fondaparinux is an indirect parenteral F Xa inhibitor, and most recently approved rivaroxaban is the first oral anti-Xa inhibitor. Other anti-Xa molecules are under development for either parenteral (idraparinux, DX-9065a) or oral use (razaxaban, apixaban, rivaroxaban, LY-51, 7717, BMS-56247 a DU-176b).