While the effects of Warfarin can be reversed, some of the newer oral anticoagulants do not have direct antidotes therefore management should focus on resuscitation and factor replacement. 13 Early haematological advice from the MTS’s is recommended to guide management.
Vitamin K, given orally or intravenously (Phytomenadione) can be used to accelerate Warfarin reversal by counteracting its effects on Vitamin K-dependent coagulation factor synthesis. 6 The intravenous route achieves a more rapid response compared with oral administration, with an onset of action seen within 6-8 hours.1 Its effect is not immediate but will progress over time as the liver synthesises sufficient quantities of coagulation proteins (factors II, VII, IX, X) dependant on Vitamin K. The usual does is 5-10mg IV given as a bolus dose.
Fresh Frozen Plasma (FFP)
Replacement is required to correct the low levels of factors II, VII, IX and X induced by warfarin. FFP contains all coagulation factors present in whole blood but it is not a factor concentrate therefore multiple units may be required. The use of plasma requires the treating facility to have appropriate facilities for frozen plasma storage and thawing. The patients’ blood group must be determined (or group AB plasma may be used) and the time taken for infusion are all be factors to be considered.1
Tranexamic Acid (TXA)
Consideration of the use of the anti-fibrinolytic agent TXA IV 15-30mg/kg, followed by a continuous infusion at 1mg/kg/hr until bleeding is under control in Factor Xa inhibitors. There is limited evidence of the clinical benefit for TXA in this setting and treatment should not delay resuscitative efforts.14
Prothrombinex-VF is the only PCC product currently available for use in Australia and NZ for warfarin reversal. It is a three factor PCC (II, IX and X) with low levels of factor VII. Prothrombinex-VF can be rapidly reconstituted into a small volume for infusion over a few minutes with a fast onset of action. The early use of PCC is recommended for the emergency reversal of Vitamin K dependant oral anticoagulants (Warfarin). Prothrombinex-VF is able to completely reverse an elevated INR within 15 minutes but due to the short half-life should be supplemented with Vitamin K to sustain the effect.1 In patients with life threatening bleeding, supplementing factor VII by administration of FFP should ensure optimal reversal of the anticoagulant effect of warfarin. Reversal of Direct Factor Xa inhibitors (Rivaroxaban, Apixaban) cannot be achieved with PCC however, small doses of PCC will optimise coagulation in the presence of vitamin K deficiency or unknown co-administration of vitamin K antagonists and may act as a partial bypassing agent in very high doses and can be considered in extreme cases. PCC is not suggested for use in patients being treated with direct thrombin inhibitors (Dabigatran). 15 A specific reversal agent, Idarucizumab, is available in some centres for reversal of Dabigatran (see below). The use of PCC does carry the increased risk of venous and arterial thrombosis during the recovery period, therefore careful consideration of its use should be weighed against the need for rapid correction of coagulopathy.
Recombinant Factor VIIa – rFVIIa (Novoseven)
rFVIIa is a novel agent used to control intractable haemorrhage. rFVIIa promotes the formation of clots by activating the extrinsic clotting cascade which leads to thrombin converting fibrinogen to fibrin. Ideally, the following should be present before rFVIIa administration:
platelets >50 x 10E9/L
An IV Bolus of 50mcg/kg may be trialled if critical bleeding from Factor Xa inhibitors. Each hospital setting will have its own local procedure for the use of Novoseven in the management of life threatening bleeding.
Idarucizumab is a monoclonal antibody fragment which binds free and thrombin-bound dabigatran and neutralises its activity, resulting in complete reversal of the anticoagulant effect. Its effect is immediate and lasts for 24 hour. 16 The complete dose of 5g should be given as two consecutive IV infusions over 5-10 minutes each. As it is a fairly new drug on the scene, its availability is limited and in Victoria is only located at The Alfred and Royal Melbourne Major Trauma Centres.