CC BY 4.0 · TH Open 2019; 03(03): e306-e308
DOI: 10.1055/s-0039-1697642
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Georg Thieme Verlag KG Stuttgart · New York

The (Fab)ulous Destiny of Idarucizumab: Highlighting Its Interference with Urine Protein Immunofixation

Nicolas Gendron
1   Laboratoire d'Hématologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France
2   Université de Paris, INSERM, U1148, Paris, France
,
Héloïse Flament
3   Laboratoire d'Immunologie-Hématologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France
4   Université de Paris, INSERM, U1149, Paris, France
,
Elena Litvinova
3   Laboratoire d'Immunologie-Hématologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France
4   Université de Paris, INSERM, U1149, Paris, France
,
Sofia Ortuno
5   Service de Néphrologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France
,
Nadine Ajzenberg
1   Laboratoire d'Hématologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France
2   Université de Paris, INSERM, U1148, Paris, France
,
Dorothée Faille
1   Laboratoire d'Hématologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France
2   Université de Paris, INSERM, U1148, Paris, France
› Author Affiliations
Further Information

Publication History

15 April 2019

05 August 2019

Publication Date:
16 September 2019 (online)

Abstract

Idarucizumab is a humanized antigen binding fragment (Fab) of a recombinant anti-dabigatran monoclonal antibody (IgG1-kappa) that allows rapid and sustained reversal of dabigatran-induced anticoagulation in case of bleeding or urgent surgery. Herein, we report a very unusual case of dabigatran reversal by idarucizumab in a 79-year-old woman with acute kidney failure admitted to a hospital in a context of hemoptysis. Three repeated injections were necessary because of massive dabigatran overdose and high rebounds of dabigatran plasma concentration. Idarucizumab was found on urine immunofixation up to 6 days after the last injection where it reacted with anti-kappa light chain antibody, but not with anti-gamma heavy chain antibody. Physicians should be aware of the increased half-life of idarucizumab in this context of acute kidney impairment and of its interference with urine immunofixation because it could lead to false-positive results and misdiagnosis of a paraprotein.

 
  • References

  • 1 Schiele F, van Ryn J, Canada K. , et al. A specific antidote for dabigatran: functional and structural characterization. Blood 2013; 121 (18) 3554-3562
  • 2 Glund S, Stangier J, Schmohl M. , et al. Safety, tolerability, and efficacy of idarucizumab for the reversal of the anticoagulant effect of dabigatran in healthy male volunteers: a randomised, placebo-controlled, double-blind phase 1 trial. Lancet 2015; 386 (9994): 680-690
  • 3 Pollack Jr CV, Reilly PA, van Ryn J. , et al. Idarucizumab for dabigatran reversal: full cohort analysis. N Engl J Med 2017; 377 (05) 431-441
  • 4 Glund S, Gan G, Moschetti V. , et al. The renal elimination pathways of the dabigatran reversal agent idarucizumab and its impact on dabigatran elimination. Clin Appl Thromb Hemost 2018; 24 (05) 724-733
  • 5 Gendron N, Gay J, Lemoine M, Gaussem P, Lillo-Le-Louet A, Smadja DM. Usefulness of initial plasma dabigatran concentration to predict rebound after reversal. Haematologica 2018; 103 (05) e226-e229