Anti-Coagulants
Warfarin (Coumadin®)
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Inhibits Vitamin K-dependent clotting Factors II, VII, IX, and X, as well as proteins C and S
- Effects are gradual and may take 2-3 days to deplete Factors and protein C and S
- Monitored via PT/INR
Heparin
- Activates Anti-thrombin
- Monitored via PTT
Low-molecular-weight Heparin (LMWH)
- Enoxaparin (Lovenox®)
- Fondaparinux (Arixtra®) - synthetic Factor Xa inhibitor chemically similar to LMWH
Dabigatran (Pradaxa®)
- Inhibits thrombin
- Idarucizumab (Praxbind®) is only FDA approved reversal agent
Rivaroxaban (Xarelto®) and Apixaban (Eliquis®)
- Inhibit only Factor Xa
- Anti-coagulant effects are immediate
- Reverse with PCC
Anti-Platelet Agents
Aspirin
- Blocks thomboxane to inhibit platelet aggregation
- Contra-indicated in patients under age 12 due to risk of Reye's Syndrome
Platelet ADP inhibitors
- Clopidigrel (Plavix®)
- Ticagrelor (Brilinta®)
Reversal Agents
Vitamin K
- Increases hepatic production of vitamin K-dependent clotting factors
- Takes 6-8 hours for INR to drop
- Takes 12-24 hours for full therapeutic effect
- IV infusion may induce anaphylactoid reactions (slow, dilute infusions may minimize)
FFP (Fresh frozen plasma)
- Separated from whole human blood
- Stored frozen - normally takes 45 minutes to defrost
- Used for Factor V deficiency, anti-thrombin III deficiency, serious bleeding on warfarin
- May also be used in massive transfusion protocols (MTP)
Protamine
- Reversal agent for heparin
- Reversal agent for Lovenox® but less effective than for heparin
Prothrombin complex concentrate (PCC)
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Manufactured from plasma pools and then lyophilized (therefore does not need to be stored frozen)
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Combination of Factors II, VII (variable concentrations by brand), IX and X, as well as proteins C and S
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Protein C and S (PCC may also contain heparin) act to limit risk of thrombosis from infusion of Factors
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USA - Profilnine SD® and Bebulin VH® (three-factor PCC), Kcentra® (four-factor PCC)
- Used for serious bleeding in patients on coumadin, Factor deficiency (from liver disease or hemophilia or congenital)
- Contra-indicated in DIC or HIT
Recombinant Factor VIIa (NovoSeven®)
- Glycoprotein made with recombinant DNA
- Indicated in Hemophilia A (Factor VIII) and B (Factor IX, Christmas disease)
- May have role in reversal of dabigatran, rivaroxaban, or apixaban
Idarucizumab (Praxbind®)
- Mono-clonal Ab that binds Dabigatran (Pradaxa®)
Platelets
- Used for reversal of anti-platelet agents (aspirin, clopidigrel)
- Stored at room temperature and have short shelf life
- May also be used in massive transfusion protocols (MTP)
- Contra-indicated in TTP
Desmopressin (DDAVP)
- Stimulates release of vWF from endothelial cells
- Also used in Hemophilia A and thrombocytopenia
- Not effective for Hemophilia B
Tranexamic acid (TXA)
- Synthetic analog lysine with anti-fibrinolytic activity
- Generally used with massive blood loss from trauma or during surgery
- May be helpful in hemoptysis
- Dilute 1 gram of TXA in 100 mL of 0.9% NS
- Nebulize over 30-45 minutes
Factors / Proteins
Protein C
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Vitamin K-dependent zymogen (inactive enzyme) activated by Thrombin
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Once active has regulatory function in anti-coagulation
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Deficiency predisposes to venous thrombosis
Protein S
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Vitamin K-dependent glyco-protein
- Fucntions as a co-factor for activated form of Protein C
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Deficiency predisposes to venous thrombosis
Factor V
- Made in the liver
- Co-factor helping to activate thrombin
- Degraded by Activated Protein C
- Factor V Leiden - genetic disorder that leads to increased risk of hyper-coagulability