The coagulation cascade is a series of enzymatic reactions that turns inactive precursors into active factors. The end result of the cascade is the production of fibrin (factor Ia), a protein that binds platelets and other materials in a stable clot. The cascade has 2 initial pathways: the extrinsic (tissue factor-mediated) and the intrinsic (contact system-initiated). These 2 pathways converge to become the common pathway with the activation of factor X (see figure below).1
Role of Antithrombin: The Coagulation Cascade
In addition to thrombin and factor Xa, AT inactivates other components of the coagulation cascade including factors IXa, XIa, XIIa, kallikrein, and the fibrinolytic plasmin.2
A Simplified Diagram of the Coagulation Cascade

References:
- Escobar CE, Harmening DM, Joiner Maier DM, Simmons VL, Smith-Moore KM, Wyrick-Glatzel J. Introduction to hemostasis. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: FA Davis Company; 2002:441-470.
- Kottke-Marchant K, Duncan A. Antithrombin deficiency: issues in laboratory diagnosis. Arch Pathol Lab Med. 2002;126(11):1326-1336.