Clinical efficacy and safety of fondaparinux in the prevention and treatment of venous and arterial thrombosis

Author:

Decousus Hervé1,Rivron-Guillot Karine2,Girard Gaelle3,Moulin Nathalie3

Affiliation:

1. Inserm, CIE3, 42055 Saint-Etienne, France; Univ Saint-Etienne, Groupe de Recherche sur la Thrombose, (EA3065), Saint-Etienne, F-42023, France; CHU Saint-Etienne, Service de Médecine Interne et Thérapeutique, Saint-Etienne, F-42055 France.

2. Inserm, CIE3, 42055 Saint-Etienne, France; Univ Saint-Etienne, Groupe de Recherche sur la Thrombose, (EA3065), Saint-Etienne, F-42023, France; CHU Saint-Etienne, Service de Médecine Interne et Thérapeutique, Saint-Etienne, F-42055 France

3. CHU Saint-Etienne, Service de Médecine Interne et Thérapeutique, Saint-Etienne, F-42055 France

Abstract

Fondaparinux (Arixtra®) is a synthetic, selective Factor Xa inhibitor. Its pharmacokinetic profile allows once-daily subcutaneous administration of the drug without any laboratory monitoring. The benefit-to-risk ratio of fondaparinux in the prevention of venous thromboembolism has been extensively studied in both surgical and acutely ill medical patients at risk of thrombosis. Its efficacy and safety have also been investigated in the initial treatment of symptomatic deep-vein thrombosis and pulmonary embolism. Finally, a number of Phase II trials investigated the safety and efficacy of fondaparinux in patients with acute coronary syndromes, and a large Phase III program is ongoing in this setting. This review focuses on the use of fondaparinux in the prevention and treatment of thromboembolic disorders.

Publisher

Future Medicine Ltd

Subject

Cardiology and Cardiovascular Medicine,Molecular Medicine

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