![]() UFH and LMWH bind and activate antithrombin, which acts to inhibit factor IIa (thrombin) and factor Xa, inhibiting further progression of the clotting cascade. Unfractionated heparin (UFH) and low-molecular weight heparin (LMWH) are often used in acute thrombosis because of their rapid onset of action and effectiveness. Overview of the coagulation cascade, indicating the sites of action of anticoagulant medications and their reversal agents.Īnticoagulants are important drugs used as the primary intervention for the prevention and treatment of thrombosis ( Table 1). ![]() They are poised to replace traditional anticoagulants including warfarin. Conclusions: A new generation of anticoagulants, the DOACs, and their reversal agents, are gaining prominence in clinical practice, having demonstrated superior efficacy and safety profiles. Additionally, ciraparantag, a potential “universal” reversal agent, is currently under clinical development. Two reversal agents have been approved within the last five years: idarucizumab for the reversal of dabigatran, and andexanet alfa for the reversal of rivaroxaban and apixaban. These DOACs all have a rapid onset of action and each has a predictable therapeutic response requiring no monitoring, unlike the older anticoagulants, such as warfarin. Results: The DOACs include the direct thrombin inhibitor-dabigatran, and the factor Xa inhibitors-rivaroxaban, apixaban, edoxaban, and betrixaban. ![]() ![]() Methods: Published literature was searched, and information extracted to provide an update on DOACS and their reversal agents. Like the older generation anticoagulants, DOACs require specific reversal agents in cases of life-threatening bleeding or the need for high-risk surgery. Background: Over the last ten years, a new class of drugs, known as the direct-acting oral anticoagulants (DOACs), have emerged at the forefront of anticoagulation therapy. ![]()
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