Use of tranexamic acid in dogs with primary immune thrombocytopenia: A feasibility study

ObjectiveThe aim of this feasibility study is to evaluate the use of tranexamic acid and its safe use alongside standard therapy in dogs with primary immune thrombocytopenia (ITP).DesignThis is a cohort feasibility study involving 10 dogs diagnosed with primary ITP that received standard therapy for...

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Main Authors: Gerard Olivares, Mellora Sharman, Rachel Miller, Caroline Kisielewicz, Mayank Seth
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-03-01
Series:Frontiers in Veterinary Science
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fvets.2023.946127/full
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author Gerard Olivares
Gerard Olivares
Mellora Sharman
Rachel Miller
Caroline Kisielewicz
Mayank Seth
author_facet Gerard Olivares
Gerard Olivares
Mellora Sharman
Rachel Miller
Caroline Kisielewicz
Mayank Seth
author_sort Gerard Olivares
collection DOAJ
description ObjectiveThe aim of this feasibility study is to evaluate the use of tranexamic acid and its safe use alongside standard therapy in dogs with primary immune thrombocytopenia (ITP).DesignThis is a cohort feasibility study involving 10 dogs diagnosed with primary ITP that received standard therapy for ITP including corticosteroids, a single dose of vincristine, and omeprazole. Dogs were randomly divided into either the control group (n = 6) or the group receiving tranexamic acid (TXA group, n = 4).Key findingsThe mean time from the start of treatment until remission was 5 days in the TXA group and 6 days in the control group (P = 0.69). Two dogs, one in each group, did not achieve remission. Clinical bleeding scores were not significantly different between both groups (p = 0.43), and the median blood volume administered was 37.5 ml/kg for the TXA group and 9.72 ml/kg for the control group (p = 0.084). Three out of the four dogs receiving TXA of 20 mg/kg IV started vomiting within 15 min of administration and were given a reduced dose of 15 or 10 mg/kg IV.ConclusionTranexamic acid did not confer a clinical benefit in this small cohort study and was associated with a high incidence of vomiting. This study provides useful information for the design of future trials in dogs with ITP receiving tranexamic acid including outcome measures and safety.
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spelling doaj.art-a8633da7c2a541369772e30076f375902023-03-22T06:07:15ZengFrontiers Media S.A.Frontiers in Veterinary Science2297-17692023-03-011010.3389/fvets.2023.946127946127Use of tranexamic acid in dogs with primary immune thrombocytopenia: A feasibility studyGerard Olivares0Gerard Olivares1Mellora Sharman2Rachel Miller3Caroline Kisielewicz4Mayank Seth5Department of Small Animal Internal Medicine, Animal Health Trust, Newmarket, Suffolk, United KingdomDepartment of Small Animal Internal Medicine, Eastcott Veterinary Referrals, Part or Linnaeus Veterinary Limited, Swindon, United KingdomDepartment of Small Animal Internal Medicine, Animal Health Trust, Newmarket, Suffolk, United KingdomDepartment of Small Animal Internal Medicine, Dick White Referrals, Cambridgeshire, United KingdomDepartment of Small Animal Internal Medicine, Pride Veterinary Centre, Derby, United KingdomDepartment of Small Animal Internal Medicine, Animal Health Trust, Newmarket, Suffolk, United KingdomObjectiveThe aim of this feasibility study is to evaluate the use of tranexamic acid and its safe use alongside standard therapy in dogs with primary immune thrombocytopenia (ITP).DesignThis is a cohort feasibility study involving 10 dogs diagnosed with primary ITP that received standard therapy for ITP including corticosteroids, a single dose of vincristine, and omeprazole. Dogs were randomly divided into either the control group (n = 6) or the group receiving tranexamic acid (TXA group, n = 4).Key findingsThe mean time from the start of treatment until remission was 5 days in the TXA group and 6 days in the control group (P = 0.69). Two dogs, one in each group, did not achieve remission. Clinical bleeding scores were not significantly different between both groups (p = 0.43), and the median blood volume administered was 37.5 ml/kg for the TXA group and 9.72 ml/kg for the control group (p = 0.084). Three out of the four dogs receiving TXA of 20 mg/kg IV started vomiting within 15 min of administration and were given a reduced dose of 15 or 10 mg/kg IV.ConclusionTranexamic acid did not confer a clinical benefit in this small cohort study and was associated with a high incidence of vomiting. This study provides useful information for the design of future trials in dogs with ITP receiving tranexamic acid including outcome measures and safety.https://www.frontiersin.org/articles/10.3389/fvets.2023.946127/fulltranexamic acidcaninebleeding scoreimmune thrombocytopenia (ITP)antifibrinolytics
spellingShingle Gerard Olivares
Gerard Olivares
Mellora Sharman
Rachel Miller
Caroline Kisielewicz
Mayank Seth
Use of tranexamic acid in dogs with primary immune thrombocytopenia: A feasibility study
Frontiers in Veterinary Science
tranexamic acid
canine
bleeding score
immune thrombocytopenia (ITP)
antifibrinolytics
title Use of tranexamic acid in dogs with primary immune thrombocytopenia: A feasibility study
title_full Use of tranexamic acid in dogs with primary immune thrombocytopenia: A feasibility study
title_fullStr Use of tranexamic acid in dogs with primary immune thrombocytopenia: A feasibility study
title_full_unstemmed Use of tranexamic acid in dogs with primary immune thrombocytopenia: A feasibility study
title_short Use of tranexamic acid in dogs with primary immune thrombocytopenia: A feasibility study
title_sort use of tranexamic acid in dogs with primary immune thrombocytopenia a feasibility study
topic tranexamic acid
canine
bleeding score
immune thrombocytopenia (ITP)
antifibrinolytics
url https://www.frontiersin.org/articles/10.3389/fvets.2023.946127/full
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