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Abstract
Context: An overdose of oral anticoagulants represents a challenging scenario for emergency physicians. Dabigatran, an oral direct thrombin inhibitor, is increasingly used in place of warfarin. The lack of an antidote is a concern in patients who overdose on dabigatran, even though the drug can be eliminated with hemodialysis. Idarucizumab is an antibody fragment that binds dabigatran with high affinity. It reverses the anticoagulant effect of dabigatran within minutes and is approved for the reversal of dabigatran during emergency situations.
Case details: We describe the use of idarucizumab in the management of a 68-year-old woman who was taking dabigatran 150 mg twice daily and ingested 125 capsules. Despite gastric lavage and administration of activated charcoal within two hours of drug intake, the activated partial thromboplastin time (aPTT) and prothrombin time (PT) remained prolonged. The administration of 5 g of intravenous idarucizumab promptly and completely reversed the anticoagulant activity of dabigatran as assessed by routine and specific coagulation assays (aPTT from to 75 to 26 s, PT from 26 to 11 s and diluted thrombin time from 92 to 27 s). The initially planned emergency hemodialysis was canceled.
Discussion: This case highlights the potential use of idarucizumab for the management of massive dabigatran overdoses.
Disclosure statement
These authors have no conflicts of interest to declare.
Funding information
Marijke Peetermans and Laurens Liesenborghs receive a grant from the Research Foundation Flanders (FWO-Vlaanderen, 11I0113N and 11S5416N). Paul Reilly is employed by Boehringer Ingelheim. Charles Pollack reports receiving scientific consulting fees from Boehringer Ingelheim, Janssen, Daiichi-Sankyo and BMS/Pfizer. Marc Jacquemin reports research support from Bayer, Baxalta, Pfizer and Instrumentation Laboratories. Jerrold H. Levy has participated in steering committees for Boehringer Ingelheim, CSL Behring, Grifols, Instrumentation Laboratories and Janssen. Jeffrey I. Weitz has served as a consultant and has received honoraria from Bayer, Johnson & Johnson, Bristol-Myers Squibb, Pfizer, Boehringer Ingelheim, Daiichi Sankyo, Portola, and ISIS Pharmaceuticals. Peter Verhamme reports receiving consulting fees and/or research support from Boehringer Ingelheim, Bayer-Healthcare, Daiichi-Sankyo, and Pfizer.