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Cholestatic liver injury as a side-effect of dabigatran and the use of coagulation tests in dabigatran intoxication and after reversal by idarucizumab in bleeding and sepsis
Authors:Willemijn J Comuth  Anne-Mette Haase  Linda Ø Henriksen  Jerzy Malczynski  Daan van de Kerkhof  Anna-Marie B Münster
Institution:1. Department of Clinical Biochemistry, Hospital Unit West, Herning and Holstebro, Denmark;2. Department of Cardiology, Hospital Unit West, Herning, Denmark;3. Faculty of Health, Institute of Clinical Medicine, Aarhus University, Aarhus, Denmark;4. wilcom@rm.dk;6. Department of Medicine, Hospital Unit West, Herning, Denmark;7. Department of Cardiology, Hospital Unit West, Herning, Denmark;8. Department of Clinical Biochemistry, Catharina Hospital, Eindhoven, the Netherlands;9. Unit for Thrombosis Research, University of Southern Denmark, Esbjerg, Denmark;10. Department of Clinical Biochemistry, Hospital of South West Denmark, Esbjerg, Denmark
Abstract:Idarucizumab, an antidote specific for dabigatran, became available recently. Dabigatran is not associated with increased risk of hepatotoxicity in comparison with warfarin, but it is seen as a rare side-effect. Cases of cholestatic liver injury due to dabigatran have not been reported previously. We present a case of severe gastro-intestinal bleeding with underlying dabigatran intoxication in a patient with renal failure and the effect of reversal of dabigatran using idaruzicumab on coagulation assays. International normalized ratio (INR) and activated partial thromboplastin time (APTT) results were elevated in a setting of sepsis, possibly due to liver failure. INR and APTT can be elevated if sepsis is complicated by disseminated intravascular coagulation (DIC) or liver failure, making it challenging to determine dabigatrans contribution to their prolongation. A rebound effect after administration of idarucizumab and slow elimination of dabigatran due to reduced kidney function could be detected using the Hemoclot® diluted thrombin time (dTT) in this situation, in contrast to with non-dilutional assays. Before admission, cholestatic liver injury started shortly after initiation of dabigatran etexilate therapy. As no other cause was found, this liver injury was likely to be drug-induced. Bleeding cessated promptly after administration of idarucizumab in dabigatran intoxication. In conclusion, the anticoagulant effect of dabigatran can be measured by Hemoclot® dTT in sepsis and cholestatic liver injury was seen as a possible rare side-effect of dabigatran treatment.
Keywords:Antidotes  blood coagulation tests  dabigatran  chemical and drug induced liver injury  sepsis  haemorrhage  anticoagulants  activated partial thromboplastin time  blood coagulation  prothrombin time  international normalized ratio  thrombin time
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