Until recently, warfarin (also known as Coumadin), a vitamin K antagonist (VKA), had been the only available oral anticoagulant. The use of warfarin has been always complicated by many issues including its narrow therapeutic index and multiple drug and diet interactions affected its safety, compliance, and efficacy. Patients needed regular and close monitoring of the its anticoagulant effect (how thin is blood?). Despite regular monitoring, patients suffered bleeding complications when blood was too thin (supra-therapeutic range) or blood was thin within the desired range but other patient factors (such as trauma/injury) resulted in bleeding.
A very common use of warfarin is for anticoagulation in patients who suffer from atrial fibrillation. With increasing age, the risk of atrial fibrillation increases and atrial fibrillation is common older individuals. Patients with atrial fibrillation can develop a clot in the left atrium of the heart and this clot can dislodge and go to other parts of the body. If this dislodged clot goes to arteries that supply blood to the brain, it usually results in large stroke. The risk of stroke with atrial fibrillation varies from person to person but can be calculated using a CHADS2 score and may vary from 1.8% per year to 18% per year without anticoagulation.
The above noted problems with warfarin prompted the development of new oral anticoagulants that target key coagulation proteins. Within past few years, FDA has approved several new oral anticoagulants that don’t require regular monitoring with blood tests and have very few drug interactions. However, one limitation with these new anticoagulants is lack of an antidote that can quickly reverse the effect of these drugs in cases of emergency, such as when a patient is bleeding. On the other hand, vitamin K can be used to reverse the effect of warfarin. Several pharmaceutical companies and other research groups are trying to develop agents that can effectively reverse the effects of these new anticoagulants.
Pollack and colleagues have published in this issue of the New England Journal of Medicine a trial of such an antidote of dabigatran, an oral thrombin inhibitor that is approved for the prevention of stroke in patients with non-valvular atrial fibrillation and for the prevention and treatment of venous thromboembolism. Investigators used idarucizumab, a monoclonal antibody fragment that binds dabigatran with an affinity that is 350 times as high as that of dabigatran’s affinity with thrombin (a coagulant protein through which dabigatran acts). In blood, idarucizumab binds free and thrombin-bound dabigatran and neutralizes its activity. In this prospective cohort study, investigators examined the safety of 5 g of intravenous idarucizumab and its inhibitory effect on dabigatran in patients who had serious bleeding (group A) or who required an urgent procedure (group B). Investigators determined the maximum percentage reversal of the anticoagulant effect of dabigatran within 4 hours after the administration of idarucizumab (primary endpoint).
Of the 90 patients who received idarucizumab (51 patients in group A and 39 in group B), idarucizumab normalized the blood coagulation in 88 to 98% of the patients often within minutes. Concentrations of unbound dabigatran was below 20 ng per milliliter at 24 hours in 79% of the patients. Among 35 patients in group A who could be assessed, bleeding was controlled at a median of 11.4 hours. Among 36 patients in group B who underwent a procedure, normal intraoperative hemostasis was reported in 33, and mildly or moderately abnormal hemostasis was reported in 2 patients and 1 patient, respectively. One thrombotic event occurred within 72 hours after idarucizumab administration in a patient in whom anticoagulants had not been reinitiated.
As noted above idarucizumab is specific for dabigatran and is unlikely to be effective with other new oral antocagulants. However, various reversal agents and/or strategies, nonspecific to dabigatran, are available to physicians, including prothrombin complex concentrates, activated prothrombin complex concentrates, or recombinant factor VIIa.
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