Hypercoagulability Flashcards
Antithrombin Deficiency
Inherited deficiency of antithrombin, no direct effect on PT, PTT, or thrombin time but diminishes the increase of PTT following heparin administration because heparin usually activates antithrombin
Factor V Leiden (what it is, demographic)
Production of mutant factor V resistant to degradation by activated Protein C
Most common inherited hypercoagulability, especially in whites
Protein C or S Deficiency
Normally inactivate factors V and VIII (accelerating factors) but can’t now. Increases risk for thrombotic skin necrosis with hemorrhage following administration of warfarin (because eliminates what little C and S you have)
Prothromin gene mutation
Point mutation causes increased production leading to more thrombin/clots