Anticoagulants are used to interfere with hemostasis (stop bleeding) and prevent the formation of thrombi. They suppress coagulation by reducing the formation of fibrin
Fibrin is a tough protein that forms a mesh around the clot and solidifies it
Indications for anticoagulants
treat DVT and PE
prevent VTE and thrombosis with atrial fibrillation and prosthetic heart valves
prevent complications with MI
Anticoagulant act on the third step of hemostasis. Coagulation is when fibrin forms a mesh that traps red blood cells and platelets, forming the clot
There are 2 factors in hemostasis:
factors affected by warfarin (vitamin K dependent clotting factor)
factor affected by heparin (factor that can be inactivated by antithrombin)
Fibrinolysis is a mechanism by which formed thrombi are lysed. Anticoagulants do not lyse thrombi, they prevent them from bigger
There are 4 types of anticoagulants
unfractioned heparin (heparin)
low molecular weight heparin (dalteparin, enoxaparin and tinzaparin)
vitamin K antagonist (warfarin)
direct oral anticoagulants (thrombin inhibitors like dabigatran) and factor Xa inhibitors like apixaban)
Action of unfractioned heparin: enhance the activity of antithrombin by inactivating thrombin and factor Xa and reducing the production of fibrin
Unfractioned heparin is only administered by injection. Its therapeutic response is to prevent DVT and PE and permit adequate anticoagulation
Adverse effects of unfractioned and LMW heparin
bleeding
heparin induced thrombocytopenia (low level of platelets increasing the risk of bleeding)
antidote: protamine sulfate
Anticoagulants are not indicated for patients with thrombocytopenia since it increases the risk of bleeding
Unfractioned heparin needs aPTT monitoring, a blood test measuring the time it takes for the blood to clot. Heparin increases aPTT to around 60 to 80 seconds
Administration of heparin and LMW heparin
independent double verification
favor abdomen as injection site
rotate sites at each injection
do not massage injection site
LMW heparin enhances the activity of antithrombin by inactivating factor Xa over thrombin (predictable response) and reducing fibrin production
Manifestations of bleeding are bleeding gums, petechiae (type of rash), ecchymosis, black tarry stools, hematuria, low BP and low hematocrit
LMW heparin like dalteparin does not require aPTT since plasma levels are highly predictable
Vitamin K angonist inhibitis the synthesis of vitamin K dependent clotting factors and reduces fibrin production
Bridging atnicoagulants means administering 2 anticoagulants at the same time while warfarin (vitamin K antagonist) reaches its peak
Warfarin labatory monitoring is done with PT (prothrombin time) and INR (international normalized ratio). Target INR is 2-3 for VTE and 3 for mechanical mitral valve. It is measured frequently initially to allow dosage adjustment
Adverse affects of warfarin
bleeding
antidote is vitamin K
Direct oral anticoagulants direct the inhibition thrombin and factorXa (reduction of fibrin)
Dabigatran is a thrombin inhibitor vs apixaban is a factor Xa inhibitor. They are used to prevent or treat VTE and to prevent strokes
Direct anticoagulant adverse effects
bleeding
antidote is praxbind or ondexxya
Direct oral anticoagulant do not require anticoagulant monitoring since plasma levels are highly predictable
Nursing implications of anticoagulants
monitor for signs of bleeding
rotate injection sites
education on soft toothbrush and electric razor
notify if invasive procedure
for warfarin: maintain constant intake of vitamin K