Page 1068 - Cote clinical veterinary advisor dogs and cats 4th
P. 1068

Icterus   529


           anemia; if significant anemia is not present   ○   Pre-hepatic:  hepatomegaly  and  spleno-  Nutrition/Diet
           (packed cell volume [PCV]  > 30% in dogs,   megaly  common  with  IMHA;  evaluate   Nutritional support is a key aspect of treatment
  VetBooks.ir  should be suspected. They are often differenti-  ○   Hepatic: hypoechoic hepatic parenchyma   is required for treatment of hepatic lipidosis,   Diseases and   Disorders
                                                                                  for some causes of icterus. Adequate nutrition
           > 25% cats), hepatic or post-hepatic icterus
                                                  for underlying cause of secondary IMHA
                                                  (infectious hepatitis, neoplastic infiltrate),
                                                                                  copper-restricted diets are necessary for copper-
           ated with a chemistry profile and abdominal
                                                  hyperechoic hepatic parenchyma (neo-
           ultrasound.
                                                  plasia), hepatic mass, large or small liver   associated hepatopathy, and fat-restricted diets
                                                                                  are appropriate for pancreatitis.
           Differential Diagnosis                 (size best assessed on radiographs), chronic
           Poor lighting or differences in visual perception   hepatopathies may have mild echogenicity   Drug Interactions
           can give a false impression of icterus; measure-  changes (hypoechoic, heterogenous) or   Hepatic  metabolism  and  biliary  excretion
           ment of total bilirubin is confirmatory.  may be normal in appearance  should be taken into account when prescrib-
                                                ○   Post-hepatic: evaluate gallbladder, common   ing medications to patients with hepatic and
           Initial Database                       bile duct, and extrahepatic structures/  post-hepatic icterus, respectively.
           The myriad causes of icterus are reflected by   organs that may result in post-hepatic
           variations in test results. Common findings:  icterus (e.g., pancreatitis, extramural   Possible Complications
           •  CBC                                 mass); peritonitis with free fluid if biliary   •  There  are  multiple  possible  complications
             ○   Pre-hepatic: anemia (often regenerative)   rupture                 for  the underlying disorders  that cause
               ± autoagglutination  ± spherocytes  ±                                icterus.
               RBC parasites  ± thrombocytopenia  ±   Advanced or Confirmatory Testing  •  In people, bilirubin accumulation in the brain
               leukocytosis                    •  Infectious disease testing, as appropriate  leads to neurologic dysfunction (kernicterus);
             ○   Hepatic: ± mild anemia ± inflammatory   ○   Pre-hepatic: vector-borne disease serology   this does not seem to be a problem in dogs
               or stress leukogram                and polymerase chain reaction (PCR) (e.g.,   or cats.
             ○   Post-hepatic: ± mild anemia ± inflamma-  babesiosis, cytauxzoonosis)
                                                                  †
               tory or stress leukogram         ○   Hepatic (dog*; cat ):  leptospirosis*   Recommended Monitoring
           •  Chemistry panel (by definition, all demon-  microscopic agglutination testing (MAT)   •  Pre-hepatic: vital parameters (as guide for
             strate hyperbilirubinemia)           and/or PCR (urine, blood), Histoplasma   transfusion  need and  indicator  or throm-
                                                                    †
             ○   Pre-hepatic: mild increase in liver enzymes   capsulatum urine antigen* , adenovirus*,   boembolism), PCV, total solids
                                                                    †
                                                                             †
                                                         †
               due to tissue hypoxia              tularemia , toxoplasmosis , calicivirus ,   •  Hepatic:  signs  of  hepatic  encephalopathy
             ○   Hepatic:  increased liver enzymes  (often   bartonellosis*         (dull  mentation,  hypersalivation  in  cats,
               proportional alanine aminotransferase   •  If  effusion  present,  abdominocentesis  and   nausea, seizures), appetite, serum biochem-
               [ALT]  >  alkaline  phosphatase  [ALP],   fluid analysis (pp. 1056 and 1343)  istry profile, abdominal effusion
               gamma-glutamyltransferase  [GGT]);  •  Ultrasound-guided  fine-needle  aspiration   •  Post-hepatic:  serum  biochemistry  profile,
               potential  for  decreased  in  synthetic   (FNA) of liver or associated masses (p. 1112)  appetite, abdominal comfort
               function (glucose, cholesterol, albumin,   ○   Often diagnostic for hepatic neoplasia
               blood urea nitrogen [BUN]); azotemia   (especially round cell neoplasia), hepatic    PROGNOSIS & OUTCOME
               with  leptospirosis.  Cats  with  hepatic   lipidosis, and some infectious diseases
               lipidosis often have normal GGT.  ○   Less useful for chronic hepatopathy,   Prognosis depends on the underlying disease
             ○   Post-hepatic: increased liver enzymes (ALP,   hepatotoxicity     process and severity of disease, ranging from
               GGT  > ALT), hypercholesterolemia,   •  Hepatic  biopsy  (ultrasound-guided needle   excellent (e.g., treatable cause of hemolysis) to
               hypertriglyceridemia             biopsy, laparoscopic, laparotomy; coagulation   grave (end-stage hepatic cirrhosis, metastatic
           •  Urinalysis:  bilirubinuria;  hemoglobinuria   profile first)        neoplasia).
             with intravascular hemolysis; proteinuria   ○   Histopathology, tissue copper quantification,
             with inflammatory or infectious disease  and tissue/bile culture if suspect cirrhosis,    PEARLS & CONSIDERATIONS
           •  Coagulation  panel  (prothrombin  time/   chronic hepatitis, copper hepatopathy, or
             partial  thromboplastin  time  [PT/aPTT]):   neoplasia (if FNA nondiagnostic)  Comments
             normal to increased (disseminated intra-  •  Exploratory  laparotomy,  if  certain  biliary   •  Serum  bilirubin  concentration  must  be
             vascular coagulation secondary to immune-  disorders  (e.g.,  bile  peritonitis)  are    greater than 2 mg/dL before icterus can be
             mediated hemolytic anemia [IMHA],   suspected                          visualized.
             severe hepatic dysfunction, or vitamin                               •  Bile acids testing is generally not useful in
             K deficiency)                      TREATMENT                           animals  with  icterus  because  it  does  not
           •  Blood  ammonia  concentration:  may  be                               help to differentiate between hepatic and
             increased with hepatic dysfunction  Treatment Overview                 post-hepatic causes of icterus.
           •  Bile acids: seldom useful in icterus; increased   Treatment depends on the underlying cause.  •  Imaging  with  abdominal  ultrasound  is
             with hepatic or post-hepatic causes                                    important to differentiate between hepatic
           •  Abdominal radiographs (may be normal)  Acute General Treatment        and post-hepatic icterus.
             ○   Pre-hepatic: check for coin (zinc) in GI   •  Pre-hepatic: RBC transfusion (packed RBCs   •  Although   theoretically   unconjugated
               tract; hepatomegaly and/or splenomegaly   or whole blood) may be necessary (p. 1169).  (indirect) bilirubin is increased more than
               may be present with hemolysis   •  Hepatic:  discontinue  hepatotoxic  drugs,   conjugated (direct) bilirubin in animals with
             ○   Hepatic: microhepatica (chronic hepatopa-  address  fluid  and  electrolyte  disorders,   hemolysis, there is little practical benefit to
               thy) or hepatomegaly (neoplasia, infectious   treat hepatic encephalopathy (p. 440), treat   testing for each type separately (as opposed
               hepatitis)                       suspected infectious disease.       to measuring total bilirubin and PCV).
             ○   Post-hepatic: mass effect in cranial abdomen;   •  Post-hepatic: bile peritonitis is considered a
               loss of  serosal detail  (pancreatitis,  bile    surgical emergency.  Technician Tips
               peritonitis)                                                       •  An initial PCV is an important test for dogs
           •  Abdominal ultrasound (most useful in dis-  Chronic Treatment          and cats presenting with icterus because a
             tinguishing between hepatic and post-hepatic   Treatment  depends  entirely  on  underlying   normal PCV helps to rule out pre-hepatic
             cause)                            disease.                             icterus.


                                                      www.ExpertConsult.com
   1063   1064   1065   1066   1067   1068   1069   1070   1071   1072   1073