- A patient who is on anticoagulation therapy is at risk for development of thrombosis after reversal of anticoagulation
- All anticoagulation reversal agents are potentially thrombogenic
- rVIIa corrects INR, but it does not correct warfarin-induced coagulopathy
- Kcentra is a 4-factor prothrombin complex concentrate (PCC) and is the only PCC FDA approved for warfarin reversal. If using 3-factor PCC, consider concomitant FFP as 3-factor PCC contains negligible quantities of FVII
- Administering PCC and rVIIa together significantly increases the risk of thrombosis
- When starting NOAC treatment for DVT, Edoxoban and Dabigatran require an initial 5-10 days of parenteral anticoagulation, whereas Apixaban and Rivaroxaban do not
- NOACs are contraindicated if INR is elevated due to liver disease; INR in this situation may not reflect antithrombotic effect
- Protamine sulfate has anticoagulant properties
- LMWH is the anticoagulant of choice in patients who are pregnant or who have active cancer
- Initiation of anticoagulation after surgical procedure should be based on thrombotic risk vs. risk of bleeding due to the procedure
- There is a lag period between reversal of anticoagulant effect and reconstitution of hemostasis
- Consider consulting with a hematologist before complete reversal
General principles of management of anticoagulant-associated bleeding, as recommended by the American Society of Hematology, are represented by the acronym HASHTI3:
- Hold anticoagulant
- Consider Antidote, if available
- Supportive treatment
- Volume resuscitation
- Hemodynamic support
- Hemostasis (Local/Surgical)
- Consider antifibrinolytic agents (aminocaproic acid, tranexamic acid)
- Transfusion
- RBCs for severe/symptomatic anemia
- Platelets for thrombocytopenia <50 x 109/L or patient on long-acting antiplatelet agent
- Investigate for bleeding source
