Is it reasonable to use a lower DOAC dose in some patients with VTE? NO

Francesco Dentali1, Chiara Fantoni2

  • 1Department of Clinical Medicine, University of Insubria - Ospedale di Circolo, Via Guicciardini 9, 21100, Varese, Italy. fdentali@libero.it.

Insights

Direct oral anticoagulants (DOACs) are recommended for venous thromboembolism (VTE) and atrial fibrillation (AF). Lower DOAC doses are not advised for VTE patients, as studies show increased recurrence risk without reduced bleeding.

Area of Science:

  • Pharmacology
  • Cardiology
  • Thrombosis

Background:

  • International guidelines favor direct oral anticoagulants (DOACs) over vitamin K antagonists for long-term anticoagulation in venous thromboembolism (VTE) and non-valvular atrial fibrillation (AF).
  • DOAC dosing guidelines recommend dose reductions for AF patients with renal impairment, low body weight, or interacting medications.
  • Unlike AF patients, dose reductions for VTE patients are generally not recommended, except for Edoxaban, based on similar criteria.

Purpose of the Study:

  • To discuss the appropriateness of lower DOAC doses in specific patient populations with VTE.
  • To evaluate the evidence regarding dose adjustments for DOACs in VTE treatment compared to AF treatment.

Main Methods:

  • Review of observational studies and randomized controlled trials (RCTs) comparing DOAC use in AF and VTE patients.
  • Analysis of real-world data on DOAC dosing and outcomes in VTE patients.

Main Results:

  • Patients with AF often present with comorbidities and polypharmacy, increasing bleeding risk, unlike typical VTE patients.
  • VTE patients treated with inappropriately low DOAC doses showed higher VTE recurrence rates.
  • The bleeding risk was comparable between VTE patients on correct and incorrect DOAC doses.

Conclusions:

  • Lowering DOAC doses in VTE patients, based on criteria used for AF, is not supported by current evidence.
  • The use of lower DOAC doses in VTE patients may be unreasonable and potentially increase the risk of adverse events like recurrence.

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