Page 1431 - Small Animal Internal Medicine, 6th Edition
P. 1431

CHAPTER 87   Disorders of Hemostasis   1403



                   TABLE 87.6                                           BOX 87.6
  VetBooks.ir  Hemostatic Abnormalities*  DOGS (%)  CATS (%)     Treatment of Dogs and Cats With Disseminated
                                                                 Intravascular Coagulation
             ABNORMALITY
                                                                  1. Eliminate the precipitating cause.
             Thrombocytopenia          90             57          2. Halt intravascular coagulation:
             Prolonged aPTT            88            100            Heparin
             Schistocytosis            76             67            •  Minidose: 5-10 IU/kg SC q8h
             Positive FDP              64             24            •  Low dose: 50-100 IU/kg SC q8h
                                                                    •  Intermediate dose: 300-500 IU/kg, SC or IV, q8h
             Prolonged OSPT            42             71            •  High dose: 750-1000 IU/kg, SC or IV, q8h
             Hypofibrinogenemia        14              5            Blood or blood products (provide AT, other anticoagu-
                                                                  lants, and clotting factors)
            aPTT, Activated partial thromboplastin time; FDP, fibrin degradation   3. Maintain parenchymal organ perfusion:
            product; OSPT, one-stage prothrombin time.              Aggressive fluid therapy
            *In 50 dogs and 21 cats with disseminated intravascular   4. Prevent secondary complications:
            coagulation (DIC) evaluated at The Ohio State University Veterinary   Oxygen
            Teaching Hospital.                                      Correction of acid-base imbalance
            From Couto CG: Disseminated intravascular coagulation in dogs
            and cats, Vet Med 94:547, 1999.                         Antiarrhythmics
                                                                    Antibiotics

            whereas the presence of FDPs and hypofibrinogenemia were   AT, Antithrombin.
            rare.
              Estrin  et al. (2006)  have described  clinical  and clinico-
            pathologic findings in 46 cats with DIC. Spontaneous bleed-  Of note, if blood and blood products were available in
            ing was present in 15% of the cats; 43 of 46 cats died or were   an unlimited supply, as is the case in most human hos-
            euthanized. The most common underlying disorders were   pitals, small animal patients with DIC would not die of
            lymphoma, other forms of neoplasia, pancreatitis, and sepsis.   hypovolemic shock. Most dogs with DIC die of pulmonary
            The median PT of nonsurvivors was more prolonged than in   or renal dysfunction. At our clinic, so-called DIC lungs
            survivors (P = 0.005). DIC in cats can result from a variety   (i.e., intrapulmonary hemorrhages with alveolar septal
            of neoplastic, infectious, and inflammatory disorders and is   microthrombi) appear to be a common cause of death in
            associated with a high case fatality rate.           these patients.
            Treatment                                            Halting Intravascular Coagulation
            Once a diagnosis of DIC has been established, or even if the   I use a dual approach to halt intravascular coagulation—the
            degree of suspicion is high that DIC is present, treatment   administration of heparin and blood or blood products. As
            should be instituted without delay. Unfortunately, no con-  noted,  heparin  is  a  co-factor  for  AT and  therefore  is  not
            trolled clinical trials have been performed in veterinary   effective in preventing the activation of coagulation unless
            medicine evaluating the effects of different treatments in   AT activity in the plasma is sufficient. Because AT activity
            dogs or cats with DIC, so this discussion reflects my personal   in animals with DIC is usually low as a result of consump-
            recommendations for the treatment of dogs with this dis-  tion and possibly inactivation, the patient should be pro-
            order (Box 87.6).                                    vided  with  sufficient  quantities  of  this  anticoagulant.  The
              Unquestionably, removing or eliminating the precipitat-  most  cost-efficient  way  of  achieving  this  is  to  administer
            ing cause constitutes the main therapeutic goal in patients   FFP. The old adage that administering blood or blood prod-
            with DIC, but this is not always possible. Conditions in   ucts to a dog with DIC is analogous to “adding logs to a
            which the precipitating causes can be eliminated or amelio-  fire” has not been true, in my experience. Therefore blood
            rated  include  a  primary  HSA  (surgical  excision),  dissemi-  or blood products should never be withheld based solely
            nated or metastatic HSA (chemotherapy), sepsis (appropriate   on this.
            antimicrobial  treatment),  and  IHA  (immunosuppressive   Heparin  has  been  used  historically  to  treat  DIC  in
            treatment). In most other situations (e.g., electrocution, heat   humans  and  dogs.  However,  controversy  still  exists  re-
            stroke,  pancreatitis),  the  cause  can  rarely  be  eliminated   garding whether it is beneficial. In my experience, the
            within a short time. Therefore the treatment of dogs with   survival rate in dogs with DIC seems to have increased
            DIC is aimed at the following:                       since I started using heparin and blood products. Al-
                                                                 though this can also be attributed to improvement in
            •  Halting intravascular coagulation                 patient  care,  I  believe  that  heparin  is  beneficial  in  such
            •  Maintaining good parenchymal organ perfusion      patients and indeed may be responsible for the increased
            •  Preventing secondary complications                survival rate.
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