Monitoring of Rivaroxaban Therapy in Hypercoagulable Dogs.

J Vet Intern Med

Department of Small Animal Clinical Sciences, School of Veterinary Medicine, University College Dublin, Dublin, Ireland.

Published: February 2025

Background: Measurement of rivaroxaban efficacy using the rivaroxaban-specific anti-Xa assay (raXa) can be used for monitoring in veterinary medicine. Detection of rivaroxaban efficacy using other hemostatic tests would make monitoring timelier and more accessible.

Objectives: Compare results of raXa with prothrombin time (PT), activated partial thromboplastin time (aPTT), fibrinogen concentration, tissue factor (TF) and kaolin-activated thromboelastography (TEG), and thrombin generation (TG) in hypercoagulable dogs.

Animals: Twelve client-owned dogs, diagnosed with hypercoagulability or thromboembolic disease, and prescribed rivaroxaban, were recruited from a tertiary referral hospital from 2020 to 2022.

Methods: Prospective clinical trial. Jugular vein blood samples were collected before treatment, and 1 week and 1-3 months after initiation of rivaroxaban therapy. Hemostatic tests were performed at each visit (3 h after rivaroxaban dosing). TG curve parameters lag time, endogenous thrombin potential (ETP), peak, and time to peak (ttpeak) were assessed.

Results: There was a significant linear relationship between raXa and PT (r = 0.74, p < 0.001), ETP (r = 0.83, p < 0.001), lag time (r = 0.87, p < 0.001), peak (r = 0.86, p < 0.001), and ttpeak (r = 0.86, p < 0.001). There was a weak linear relationship between raXa and kaolin-activated TEG parameter reaction time (R) (r = 0.49, p = 0.026). There was no significant relationship between raXa and aPTT, fibrinogen concentration and the remainder of the TEG variables (p > 0.05).

Conclusion And Clinical Importance: PT and TG correlated with raXa. PT performed at a reference laboratory appeared to be a convenient method to monitor a small cohort of dogs receiving rivaroxaban therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11836667PMC
http://dx.doi.org/10.1111/jvim.70014DOI Listing

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