Direct oral anticoagulants in the treatment of cerebral venous sinus thrombosis: a single institution's experience

Neurol Neurochir Pol. 2019;53(5):384-387. doi: 10.5603/PJNNS.a2019.0037. Epub 2019 Aug 27.

Abstract

Aim of the study: Oral anticoagulants, preferentially vitamin K antagonists (VKA), are recommended for 3-12 months in patients with cerebral venous sinus thrombosis (CVST). We present a series of patients with CVST treated with direct oral anticoagulants (DOAC).

Materials and methods: We prospectively recruited 36 patients with CVST (aged 40.3 ± 9.2 years, 58.3% female) treated with DOAC based on the physician's or patient's preferences. Functional outcome was assessed with modified Rankin Scale. Recanalisation was assessed on imaging at 3-6 months post the event. Patients were followed for a median of 30 [interquartile range (IQR) 25-37] months.

Results: After use of heparin (median: 6 days; IQR 5-8.75), patients received dabigatran (150 mg bid, n = 16 or 110 mg bid, n = 2), rivaroxaban (20 mg qd, n = 10) or apixaban (5 mg bid, n = 8) for a median of 8.5 months (IQR 6.25-12). Complete or partial recanalisation was observed in 34 cases (94.4%). Three patients (8.3%) experienced major bleeding: menorrhagia on rivaroxaban (n = 2) and gastrointestinal bleeding on dabigatran (n = 1). A favourable functional outcome was observed in 24 (66.7%) patients, without any fatality. CSVT recurred in two patients (5.6%) and two venous thromboses developed in two other patients with inherited thrombophilia after anticoagulation withdrawal.

Conclusions and clinical implications: DOACs could be an alternative to VKA in CVST patients.

Keywords: anticoagulation; bleeding; cerebral venous sinus thrombosis; direct oral anticoagulants; venous thromboembolism.

MeSH terms

  • Administration, Oral
  • Adult
  • Anticoagulants
  • Dabigatran
  • Female
  • Humans
  • Male
  • Middle Aged
  • Rivaroxaban
  • Sinus Thrombosis, Intracranial*

Substances

  • Anticoagulants
  • Rivaroxaban
  • Dabigatran