ABSTRACT
Fondaparinux (Arixtra® ), a synthetic pentasaccharide, is the first in a new class of antithrombotic agents
that selectively inhibit coagulation factor Xa. In vitro experiments demonstrated
that it is a selective inhibitor of factor Xa. In plasma, fondaparinux selectively
binds to antithrombin, catalyzes factor Xa inhibition, and thereby inhibits thrombin
generation. Its antithrombotic efficacy has been demonstrated in various animal models
mimicking venous and arterial thrombosis. In humans, its pharmacokinetic profile is
favorable, with a rapid onset of antithrombotic activity and an elimination half-life
allowing a convenient once-daily dosing regimen. In several clinical trials, fondaparinux
was more effective than the reference drug, enoxaparin, in preventing venous thromboembolism
after hip fracture, major knee, and elective hip replacement surgeries. The overall
reduction in the risk of venous thromboembolism ranged between 26.3 and 56.4%, depending
on the trial. This superior efficacy was achieved without increasing the risk of clinically
relevant bleeding. Fondaparinux also showed promising results in the treatment of
patients with venous thromboembolism and acute coronary syndromes. Thus, it is now
established that selective factor Xa inhibition is an efficient way to prevent venous
thrombosis. The advent of fondaparinux offers an opportunity to improve substantially
the management of venous thromboembolism.
KEYWORDS
Fondaparinux - pentasaccharide - antithrombin - thrombosis - antithrombotic - factor
Xa