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23 – THE BLEEDING CAT  505


           Concurrent thrombocytopenia or thrombocytopathia  Vitamin K antagonist poisoning – PT is prolonged as
           was believed to have triggered bleeding in a cat follow-  well as aPTT.
           ing modified-live virus vaccination. This would appear
                                                          DIC – thrombocytopenia is often present, in addition to
           to be an uncommon event, and is not reported in
                                                          signs of a primary disease.
           humans with Hageman trait.
                                                          Acquired factor XII deficiency has been reported in
           Humans with Hageman deficiency are at increased risk
                                                          humans but not in cats.
           for thromboembolic events as a result of a deficient fib-
           rinolytic system. It is not known if cats with Hageman
           trait and cardiomyopathy are at increased risk of arte-  Treatment
           rial thromboembolism.
                                                          None required.
           It is not known if cats with Hageman trait have blunted
           inflammatory responses.
                                                          Prognosis
           Diagnosis                                      Normal life expectancy.
           No signs of abnormal bleeding unless another disease
           process affecting hemostasis is present.       Transmission
           Hageman trait is the most common inherited coagu-  Factor XII deficiency is a heritable single-gene defect
           lation factor deficiency in cats, but prevalence is not  that is autosomal recessive.
           known. Although stated to be common, recent large retro-
           spective reviews of hemostatic disorders in sick cats
                                                          Prevention
           have not identified any cases.
                                                          Probably none is required.
           Hemostatic testing reveals normal platelet count and
           BMBT, normal PT, and markedly prolonged ACT and
           aPTT (e.g. aPTT > 50 s, often > 100 s, where the upper
                                                          MISCELLANEOUS DISEASES*
           limit of normal range is 25 s).
           Definitive diagnosis is based on quantification of fac-  Classical signs
           tor XII activity (FXII:C), similar to the diagnosis of
                                                           ● Signs of the primary disease.
           hemophilia A, and ruling-out acquired factor XII defi-
           ciency (see Circulating anti-coagulant, below).
                                                          Clinical signs
           Differential diagnosis                         Thrombocytopenia, increased ACT/aPTT/PIVKA
                                                          time, or decreased antithrombin III levels have been
           Hemophilia A, B (and C) are the main differential
                                                          noted in various diseases not typically associated with
           diagnoses for markedly prolonged ACT and aPTT as
                                                          bleeding tendencies. Diseases include hypertrophic car-
           solitary abnormalities.
                                                          diomyopathy, congenital cardiac disorders, pleural
           If a cat is presented with bleeding and a prolonged ACT  effusions not due to feline infectious peritonitis, dia-
           and aPTT are found, a judgment must be made as to  betes mellitus, hyperthyroidism, hypertension, chronic
           whether the bleeding is appropriate for the injury. For  renal failure, urinary tract infection, urethral obstruction,
           example, a cat with hemothorax and prolonged ACT  rhinitis,  Mycoplasma haemofelis infection (haemo-
           and aPTT could have hemophilia A or chest trauma and  bartonellosis), primary neurologic diseases, and non-
           Hageman trait, but in the former case there would be no  anti-coagulant toxicoses.
           evidence of injury.
                                                          DIC may be the mechanism for at least some of these
           Hemophilia B and Hageman trait have occurred con-  abnormalities. The close  interaction between the
           currently.                                     intrinsic system and inflammation via factor XII
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