ORIGINAL RESEARCH article

Front. Vet. Sci.

Sec. Veterinary Emergency and Critical Care Medicine

Volume 12 - 2025 | doi: 10.3389/fvets.2025.1561003

This article is part of the Research TopicComparative Coagulation Profiles and Clot Function in Veterinary Medicine: Unravelling Species-Specific Hemostatic Mechanisms and Fibrin Meshwork StructuresView all 4 articles

Indications and outcomes of rivaroxaban use in cats

Provisionally accepted
  • 1School of Veterinary Medicine, Murdoch University, Murdoch, Australia
  • 2Centre for Terrestrial Ecosystem Science and Sustainability, Harry Butler Institute, Murdoch University, Murdoch, Australia
  • 3Animal Referral Centre (ARC Central), Freemans Bay, Auckland, New Zealand
  • 4School of Veterinary Science, Massey University, Palmerston North, New Zealand
  • 5Small Animal Specialist Hospital (SASH), North Ryde, New South Wales, Australia

The final, formatted version of the article will be published soon.

Introduction: Use of rivaroxaban, an oral direct factor Xa inhibitor, has only been described in a small number of publications in cats. The study objective was to describe the use of rivaroxaban in a large population of hospitalised cats.Cases were retrospectively identified from June 2017 to July 2024 at 7 veterinary specialty hospitals. Any cat prescribed rivaroxaban was eligible for inclusion. Data extracted from the medical records included signalment (age, sex, breed), body weight, reason for commencing rivaroxaban, dose and duration of rivaroxaban, concurrent anticoagulant and antiplatelet therapies, potential rivaroxaban adverse effects, and outcome. Non-parametric descriptive statistics are reported.Results: 66 cats were included. Median rivaroxaban dose was 2.5 mg (Min-Max 1.25-10, Q1-Q3 2.5-5.0), equal to 0.73 mg/kg/day (Min-Max 0.28-1.87, Q1-Q3 0.53-1.0). 36 cats (54.5%) were within the suggested dose range of 0.5-1 mg/kg/day of the CURATIVE (Consensus on the Rational Use of Antithrombotics in Veterinary Critical Care) guidelines, 14 (21.2%) were below, while 16 (24.2%) were above. Median duration of rivaroxaban was 26.5 days (Min-Max 0-442, Q1-Q3 2-60). The indication for rivaroxaban administration was confirmed thrombosis (48, 72.7%), strong clinical suspicion of thrombosis (6, 9.1%), and prophylaxis (12, 18.2%). Most thrombi were arterial, including aortic thromboembolism affecting both pelvic limbs (25/54 cats with thrombosis, 46.3%), arterial thrombosis affecting a single limb (16, 29.6%), and cardiac chamber thrombus (7, 13%). Cardiac disease was the most common thrombosis risk factor (53/66, 80.3%). Other CURATIVE defined risk factors included immune mediated haemolytic anaemia in four cats (6.1%), and sepsis in one. Other thromboprophylaxis administered included clopidogrel in 58 (87.9%), dalteparin in 8 cats (12.1%), and aspirin in 4 (6.1%). Potential adverse effects prompting rivaroxaban discontinuation included one case each of vomiting, a cerebrovascular accident, gastrointestinal bleeding, and haemorrhagic pleural effusion. Forty five cats (68.2%) survived to hospital discharge, 14 (21.2%) were euthanised, two (3%) died, and five (7.6%) were taken home against medical advice Conclusions: Rivaroxaban was well tolerated in a large population of cats, predominantly prescribed for arterial thrombosis associated with cardiac disease.

Keywords: thromboprophylaxis1, aortic thromboembolism2, anticoagulant3, thrombus4, immune mediated haemolytic anaemia (IMHA)5, clopidogrel6, Consensus on the Rational Use of Antithrombotics in Veterinary Critical Care (CURATIVE)7 (Min.5-Max. 8)

Received: 15 Jan 2025; Accepted: 08 May 2025.

Copyright: © 2025 Yarsley, Sharp, Boyd, Seo and Mooney. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Claire Rebecca Sharp, School of Veterinary Medicine, Murdoch University, Murdoch, Australia

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