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Peer-reviewed veterinary case report

Eltrombopag does not improve treatment of immune low platelets in dogs

By Lee, Jeongmin et al.·Published in Journal of the American Veterinary Medical Association·2026·1Korea Animal Medical Center, South Korea·View original on PubMed

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Original publication title: Eltrombopag is well tolerated but provides no additional benefit in the treatment of canine primary immune-mediated thrombocytopenia.

Species:
dog

Plain-English summary

A 5-year-old dog diagnosed with primary immune-mediated thrombocytopenia (pITP) was treated with a combination of medications, including corticosteroids and human immunoglobulin, along with the addition of eltrombopag. While eltrombopag was well tolerated and caused fewer gastrointestinal side effects, it did not improve the dog's recovery time, hospitalization duration, or survival rates compared to standard treatments alone. The findings suggest that while eltrombopag can be safely used, it may not provide significant benefits for dogs with pITP.

People also search for: dog ITP treatment · eltrombopag for dogs · primary immune-mediated thrombocytopenia in dogs

Abstract

OBJECTIVE: To evaluate the efficacy and tolerability of eltrombopag in dogs diagnosed with primary immune-mediated thrombocytopenia (pITP). METHODS: Medical records from dogs diagnosed with pITP between January 2018 and March 2024 were retrospectively reviewed. Data collected included signalment, presenting signs, diagnostic findings, duration of hospitalization, time to platelet recovery (defined as days to achieve a platelet count ≥ 100,000/μL, with no evidence of bleeding), mortality, relapse incidence, transfusion requirements, and adverse events. Dogs were included if they received a combination of corticosteroids, vincristine, mycophenolate mofetil, and human immunoglobulin, with or without the addition of oral eltrombopag administered within 24 hours of diagnosis. Dogs were grouped on the basis of whether they did or did not receive eltrombopag (eltrombopag group vs control group), and results were compared between groups. RESULTS: 18 dogs met the inclusion criteria (control group, n = 13; eltrombopag group, 5). Median time to platelet recovery, hospitalization, transfusion needs, and mortality did not differ significantly between groups. Eltrombopag was well tolerated, and adverse events, primarily gastrointestinal, were less frequent in the eltrombopag group. CONCLUSIONS: Eltrombopag was well tolerated as part of a multimodal treatment protocol for pITP in dogs. However, it was not associated with improved platelet recovery, shorter hospitalization, or reduced mortality compared with standard therapy alone. CLINICAL RELEVANCE: This study provided evidence that eltrombopag may be safely incorporated into immunosuppressive regimens for canine pITP; however, its clinical benefit remains uncertain. Further research is required to determine its role in optimizing treatment for ITP in dogs.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/41160978/