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56  Pancreatitis in the Cat  607

               Table 56.2  Medications commonly used in the management of severe pancreatitis in the feline patient
  VetBooks.ir   Class          Drug              Mechanism             Main indication  Dose and route



                Analgesic      Buprenorphine     Opioid                Acute, severe    0.01–0.02 mg/kg SC, IM, IV, TM
                               Fentanyl          Opioid                Acute, severe    25 μg/h patch,
                                                                                        5 μg/kg IV bolus, CRI 2–4 μg/kg/h
                               Butorphanol       Opioid                Acute, severe    0.1–0.5 mg/kg SC, IM, IV
                Antiemetic     Maropitant        Neurokinin‐1 receptor   Acute, severe   1 mg/kg SC q24h,
                Antinausea                       antagonist            chronic          2 mg/kg PO q24h
                               Dolasetron or     5‐HT 3  receptor      Acute, severe    0.8–1.0 mg/kg IV q24h
                               ondansetron       antagonist
                               Metoclopramide    Dopamine D2 receptor   Acute, severe   0.2–0.5 mg/kg PO, SC, IM q6–8h,
                                                 antagonist                             1–2 mg/kg/24h CRI
                Antacid        Omeprazole        Proton pump inhibitor  Acute, severe   1.0–1.3 mg/kg PO q12h
                               Pantoprazole      Proton pump inhibitor  Acute, severe   0.7–1.0 mg/kg IV q12h
                               Ranitidine        Histamine H2 receptor   Acute, severe  0.5 mg/kg PO q12h
                                                 antagonist
               CRI, constant rate infusion; IM, intramuscular; IV, intravenous; PO, by mouth (per os); SC, subcutaneous.

               associated with shorter ICU and hospital stays, lower   chronic management approach once they are eating vol­
               total costs of care, and fewer complications during ini­  untarily and are able to be discharged.
               tial management. With cats, the potential for develop­  Cats with a clinical suspicion of chronic pancreatitis
               ment  of  hepatic  lipidosis as a complication of severe   are treated in essentially the same manner as cats with
               pancreatitis and inadequate caloric intake must also be   chronic enteropathies or diagnoses of idiopathic inflam­
               considered.  While currently there is limited informa­  matory bowel disease. There is no meaningful way to
               tion  in  the  veterinary literature regarding the use of   distinguish between chronic pancreatitis as a solitary
               early enteral nutrition in cats with severe pancreatitis,   disease entity and the presence of multiorgan inflamma­
               the  author  uses  this modality regularly, and quite   tory disease (so‐called feline inflammatory disease or
               aggressively. In many cats, assisted feeding devices such   “triaditis”). Initially, dietary modification, typically by
               as  esophagostomy  tubes are placed during the first   use of a novel protein source or hypoallergenic diet, is
               24–36 hours of hospitalization to achieve early return   suggested. In contrast to dogs, where fat restriction is a
               to feeding. For both hepatic  lipidosis  and  diabetic   cornerstone of management for most cases of chronic
               ketoacidosis, a return to caloric intake is critical to their   pancreatitis, fat restriction is not recommended in the
               successful management, and the presence of pancreati­  cat due to their high constitutive requirement for both
               tis (either as an inciting disease or a complication) does   fat and arachidonic acid intake. Many cats will respond
               not alter the importance of a return to positive caloric   to dietary manipulation; in those who fail to respond to
               balance in these diseases.                         dietary  manipulation,  it  is  rational  to  consider  antiin­
                                                                  flammatory or immune modulatory therapies, assuming
                                                                  that no other co‐morbidities are present that would con­
               Outpatient Management of Cats with                 traindicate the use of these medications.
               Chronic Pancreatitis
                                                                   A common additional finding in cats with chronic
               Cats presenting with less severe clinical signs, perhaps   pancreatitis, particularly in those with significant gastro­
               with histories of vomiting, weight loss or other gastroin­  intestinal disease accompanying their pancreatic disease,
               testinal signs but without significant abnormalities on   is the presence of hypocobalaminemia. Cats with hypoc­
               screening biochemical panels, can typically be treated on   obalaminemia (low vitamin B 12 ) are known to be less
               an outpatient basis. In these patients, collection of sam­  responsive  to treatment for other diseases, such as
               ples for specialized testing (Spec‐fPL) is recommended,   chronic inflammatory bowel disease, if this hypocobala­
               but there is less utility to the patient‐side testing, as these   minemia  is  not  addressed  via  supplementation.
               patients will be treated on an outpatient basis in the same   Supplementation of  cats with cobalamin is  straight­
               manner regardless of the initial patient‐side test result.   forward, and can be carried out using injectable or oral
               Cats  that had  originally  presented  with  a suspicion  of   supplementation regimes. In some cats, particularly
               severe pancreatitis should also transition to this more   those with diffuse small intestinal disease, serum folate
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