Heparin-resistant Thrombosis Due to Homozygous Antithrombin Deficiency Treated With Rivaroxaban: A Case Report

J Pediatr Hematol Oncol. 2016 Nov;38(8):658-660. doi: 10.1097/MPH.0000000000000608.

Abstract

Background: Heparin fulfills its anticoagulant action through activation of antithrombin (AT), and thus thrombosis secondary to AT deficiency can be associated with heparin resistance.

Observation: A 12-year-old girl with severe venous thrombosis was referred to us because of undetectable anti-Xa levels despite low-molecular-weight heparin therapy. Laboratory investigations revealed a homozygous AT mutation in the heparin binding site (AT Budapest III). She was subsequently treated with rivaroxaban successfully.

Conclusions: Heparin resistance warrants evaluation for AT deficiency. Rivaroxaban may be considered a valid anticoagulant alternative to low-molecular-weight heparin in these patients.

Publication types

  • Case Reports

MeSH terms

  • Antithrombin III / analysis
  • Antithrombin III Deficiency / complications*
  • Binding Sites / genetics
  • Child
  • Drug Resistance / genetics
  • Factor Xa Inhibitors
  • Female
  • Heparin, Low-Molecular-Weight / pharmacology*
  • Heparin, Low-Molecular-Weight / therapeutic use
  • Humans
  • Rivaroxaban / administration & dosage*
  • Thrombosis / drug therapy*

Substances

  • Factor Xa Inhibitors
  • Heparin, Low-Molecular-Weight
  • antithrombin III Budapest 2
  • Antithrombin III
  • Rivaroxaban