Haematology-Oncology · Pathway 50
Antithrombin Iii Deficiency
Key points
- Antithrombin III deficiency is an inherited cause of thrombophilia occurring in approximately 1:3,000 of the population. Inheritance is autosomal dominant. Antithrombin III inhibits several clotting factors, primarily thrombin,
- recurrent venous thromboses
- arterial thromboses do occur but are uncommon Management
- thromboembolic events are treated with lifelong warfarinisation
- heparinisation during pregnancy*