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ALL / Cardiology
Warfarin
Warfarin
Warfarin is an oral anticoagulant that was used first-line for many years in both the management of venous thromboembolism and reducing stroke risk in patients with atrial fibrillation. It has now been largely superseded by the use of direct oral anticoagulants (DOACs) which do not require the same level of monitoring as warfarin.Mechanism of action
- inhibits epoxide reductase preventing the reduction of vitamin K to its active hydroquinone form
- this in turn acts as a cofactor in the carboxylation of clotting factor II, VII, IX and X (mnemonic = 1972) and protein C.
Indications
- mechanical heart valves
- target INR depends on the valve type and location
- mitral valves generally require a higher INR than aortic valves.
- second-line after DOACs:
- venous thromboembolism: target INR = 2.5, if recurrent 3.5
- atrial fibrillation, target INR = 2.5
Monitoring
- patients are monitored using the INR (international normalised ratio), the ratio of the prothrombin time for the patient over the normal prothrombin time.
- warfarin has a long half-life and achieving a stable INR may take several days
- there are a variety of loading regimes and computer software is now often used to alter the dose
Factors that may potentiate warfarin
- liver disease
- P450 enzyme inhibitors, e.g.: amiodarone, ciprofloxacin
- cranberry juice
- drugs which displace warfarin from plasma albumin, e.g. NSAIDs
- inhibit platelet function: NSAIDs
Side-effects
- haemorrhage
- teratogenic, although can be used in breastfeeding mothers
- skin necrosis
- when warfarin is first started biosynthesis of protein C is reduced
- this results in a temporary procoagulant state after initially starting warfarin, normally avoided by concurrent heparin administration
- thrombosis may occur in venules leading to skin necrosis
- purple toes
+PassMedicine Notes
Warfarin is an oral anticoagulant that was used first-line for many years in both the management of venous thromboembolism and reducing stroke risk in patients with atrial fibrillation. It has now been largely superseded by the use of direct oral anticoagulants (DOACs) which do not require the same level of monitoring as warfarin.
Mechanism of action- inhibits epoxide reductase preventing the reduction of vitamin K to its active hydroquinone form
- this in turn acts as a cofactor in the carboxylation of clotting factor II, VII, IX and X (mnemonic = 1972) and protein C.
- mechanical heart valves
- target INR depends on the valve type and location
- mitral valves generally require a higher INR than aortic valves.
- second-line after DOACs:
- venous thromboembolism: target INR = 2.5, if recurrent 3.5
- atrial fibrillation, target INR = 2.5
- patients are monitored using the INR (international normalised ratio), the ratio of the prothrombin time for the patient over the normal prothrombin time.
- warfarin has a long half-life and achieving a stable INR may take several days
- there are a variety of loading regimes and computer software is now often used to alter the dose
- liver disease
- P450 enzyme inhibitors, e.g.: amiodarone, ciprofloxacin
- cranberry juice
- drugs which displace warfarin from plasma albumin, e.g. NSAIDs
- inhibit platelet function: NSAIDs
- haemorrhage
- teratogenic, although can be used in breastfeeding mothers
- skin necrosis
- when warfarin is first started biosynthesis of protein C is reduced
- this results in a temporary procoagulant state after initially starting warfarin, normally avoided by concurrent heparin administration
- thrombosis may occur in venules leading to skin necrosis
- purple toes
