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Journal of the American Veterinary Medical Association2014; 244(6); 719-723; doi: 10.2460/javma.244.6.719

Hemorrhage and blood loss-induced anemia associated with an acquired coagulation factor VIII inhibitor in a Thoroughbred mare.

Abstract: A 23-year-old Thoroughbred mare was evaluated because of a coagulopathy causing hemoperitoneum, hematomas, and signs of blood loss-induced anemia. Results: The mare had tachycardia, pallor, hypoperfusion, and a large mass in the right flank. The mass was further characterized ultrasonographically as an extensive hematoma in the body wall with associated hemoabdomen. Coagulation testing revealed persistent, specific prolongation of the activated partial thromboplastin time (> 100 seconds; reference interval, 24 to 44 seconds) attributable to severe factor VIII deficiency (12%; reference interval, 50% to 200%). On the basis of the horse's age, lack of previous signs of a bleeding diathesis, and subsequent quantification of plasma factor VIII inhibitory activity (Bethesda assay titer, 2.7 Bethesda units/mL), acquired hemophilia A was diagnosed. The medical history did not reveal risk factors or underlying diseases; thus, the development of inhibitory antibodies against factor VIII was considered to be idiopathic. Results: The mare was treated with 2 transfusions of fresh whole blood and fresh-frozen plasma. Immunosuppressive treatment consisting of dexamethasone and azathioprine was initiated. Factor VIII deficiency and signs of coagulopathy resolved, and the inhibitory antibody titer decreased. The mare remained healthy with no relapse for at least 1 year after treatment. Conclusions: Horses may develop inhibitory antibodies against factor VIII that cause acquired hemophilia A. A treatment strategy combining transfusions of whole blood and fresh-frozen plasma and administration of immunosuppressive agents was effective and induced sustained remission for at least 1 year in the mare described here.
Publication Date: 2014-02-27 PubMed ID: 24568115DOI: 10.2460/javma.244.6.719Google Scholar: Lookup
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Summary

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The research article discusses the diagnosis, treatment and successful management of a rare bleeding disorder known as acquired hemophilia A in a 23-year-old Thoroughbred mare.

Background

  • The horse, upon examination, showed signs of severe anemia due to blood loss which included a high heart rate, pale gums, reduced blood flow and a large swelling observed in the right flank of the horse.
  • Further ultrasonographic examination revealed the swelling to be a massive hematoma (blood-filled swelling) in the body wall leading to bleeding within the abdomen.

Diagnosis

  • Results from coagulation tests showed a prolonged activated partial thromboplastin time (aPTT), indicating an issue with blood clotting.
  • The aPTT score was significantly higher than the normal range, leading researchers to further examine clotting factors in the mare’s blood.
  • The mare was found to have seriously deficient levels of Factor VIII, which contributes to normal blood clotting.
  • Considering the mare’s age, the sudden onset of the bleeding disorder, and specific tests assessing Factor VIII inhibitory activity in the plasma, the horse was diagnosed with acquired hemophilia A. This is a rare condition caused by the idiopathic (unexplained) development of inhibitory antibodies against Factor VIII.

Treatment and Outcome

  • The mare was treated initially with transfusions of fresh whole blood and fresh-frozen plasma, to supplement the deficient Factor VIII and to correct anemia.
  • Next, an immunosuppressive treatment was introduced comprising of dexamethasone and azathioprine, to counter the activity of the inhibitory antibodies that were preventing Factor VIII from performing its normal function.
  • The treatment was successful as observed in the normalized Factor VIII levels, resolved signs of coagulopathy (bleeding disorder), and a decrease in the inhibitory antibody titer (measurement of the concentration of the antibodies).
  • The mare exhibited sustained remission for at least a year following the treatment with no signs of recurrence of the disease.

Conclusions

  • The study concludes that horses can develop acquired hemophilia A due to the emergence of inhibitory antibodies against Factor VIII..
  • The case study demonstrates how combining transfusion of fresh whole blood and fresh-frozen plasma, along with administration of immunosuppressive drugs, can effectively treat the condition and induce sustained remission.

Cite This Article

APA
Winfield LS, Brooks MB. (2014). Hemorrhage and blood loss-induced anemia associated with an acquired coagulation factor VIII inhibitor in a Thoroughbred mare. J Am Vet Med Assoc, 244(6), 719-723. https://doi.org/10.2460/javma.244.6.719

Publication

ISSN: 1943-569X
NlmUniqueID: 7503067
Country: United States
Language: English
Volume: 244
Issue: 6
Pages: 719-723

Researcher Affiliations

Winfield, Laramie S
  • Steinbeck Country Equine Clinic, 15881 Toro Hills Ave, Salinas, CA 93908.
Brooks, Marjory B

    MeSH Terms

    • Animals
    • Blood Transfusion / veterinary
    • Factor VIII / metabolism
    • Female
    • Hemophilia A / pathology
    • Hemophilia A / therapy
    • Hemophilia A / veterinary
    • Horse Diseases / pathology
    • Horses

    Citations

    This article has been cited 1 times.
    1. Satué K, Gardon JC, Muñoz A. Clinical and laboratorial description of the differential diagnoses of hemostatic disorders in the horse. Iran J Vet Res 2020 Winter;21(1):1-8.
      pubmed: 32368218