Page 564 - Small Animal Internal Medicine, 6th Edition
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536    PART IV   Hepatobiliary and Exocrine Pancreatic Disorders


            with secondary hepatopathies, particularly hyperadrenocor-  kg orally) with a meal to increase the stimulation of gallblad-
            ticism, and with small intestinal bacterial overgrowth because   der emptying. The effect of this treatment on gallbladder
  VetBooks.ir  of reduced hepatic clearance of deconjugated bile acids.   emptying has been studied but not its effect on the bile acid
                                                                 stimulation test.
            Therefore the author would recommend a liver biopsy with
                                                                   Several questions remain to be answered regarding the
            a higher cut-off value of 40 µmol/L for postprandial bile
            acids. In patients with PSS, the magnitude of elevation does   clinical use of SBA level measurement in cats and dogs.
            not correlate with the degree of shunting or severity of clini-  Investigation of individual SBA profiles in cats and dogs with
            cal signs. The change between the fasting and postprandial   various hepatobiliary diseases has provided interesting
            values likely corresponds to portosystemic shunting, either   information but no clear and specific profile for any one
            microscopic (intrahepatic) or macroscopic. There is so much   disease. Can sequential SBA levels be used to monitor a cat’s
            overlap in  fasting and postprandial SBA patterns among   or dog’s progress more precisely? Until this and other ques-
            primary hepatobiliary diseases that no definitive statement   tions are answered, the use of SBA analysis is limited to
            can be made regarding the specific causative hepatobiliary   measuring total serum values, in the absence of cholestasis
            disease. Occasionally, fasting SBA levels are higher than   and jaundice, as a sensitive and relatively specific screening
            postprandial levels, which signify nothing more than occa-  test for the presence or absence of clinically significant hepa-
            sional, normal, spontaneous gallbladder contraction in   tobiliary disease  and/or congenital or acquired portosys-
            fasting. In general, secondary hepatic diseases cause more   temic shunting. Additional diagnostic testing must always
            modest hepatobiliary dysfunction (SBA level < 100 µmol/L).   follow to identify the specific cause.
            It is very important to remember that elevation of the SBA
            level has no functional significance in a dog or cat with   Urinary Bile Acid Concentration
            jaundice of hepatic or posthepatic origin. In these cases,   Determination of bile acids accumulating in urine over time
            elevations will purely reflect cholestasis, and measuring the   can be used to assess hepatobiliary function. Urine bile acids
            SBA level does not provide any further information.  are believed to reflect average SBA concentrations during the
              For the diagnosis of congenital PSS, fasting and postpran-  interval of urine formation. Expressing urine bile acid con-
            dial SBA level determinations are recommended to enhance   centrations as a ratio with the urine creatinine concentration
            detection ability; this is because it is relatively common for   eliminates  the  influence  of  urine  concentration  and  flow.
            fasting values to be well within normal limits and for post-  Random urine sampling for bile acid determination does not
            prandial values to be as high as 10- to 20-fold higher than   require attending to the timing of an enterohepatic challenge
            normal postprandial values.                          or obtaining a sample after withholding food. Studies of
              Because the measurement  of  fasting  and postprandial   urinary bile acid concentrations have shown that they were
            SBA concentrations assesses the same functions as the   increased in dogs and cats with hepatobiliary disease and
            ammonium chloride (NH 4 Cl) tolerance test, but without   portosystemic vascular anomalies compared with dogs and
            potentially dangerous consequences, it is the preferred   cats with nonhepatic disorders, except for hepatic neoplasia
            method. As with any specially requested test, the laboratory   in dogs. The urine nonsulfated bile acid–to–creatinine ratio
            chosen should use methods verified for clinical use in the   and the urine sulfated plus nonsulfated bile acid–to–creati-
            target species and be able to provide reference ranges.  nine ratio positively correlated with SBA test results and had
              Several factors may affect SBA levels and therefore their   similar overall diagnostic performance and substantially
            interpretation. One aspect of the SBA challenge test that has   higher (dogs) or similar (cats) specificity compared with the
            not been standardized is the feeding step. The ideal quantity   SBA test. Therefore these are recommended. The urine sul-
            and composition of the test meal have not been determined.   fated bile acid–to–creatinine ratio had lower sensitivity in
            Size of the test meal and therefore consumption of the entire   dogs and cats compared with the SBA test.
            meal or only part of the meal may affect gastric emptying.
            Delayed gastric emptying could cause the peak SBA concen-  Plasma Ammonia Concentration
            tration to occur more than 2 hours later. Hastened or delayed   One test that is not included in a standard screening battery
            intestinal transit time or the presence of intestinal disease,   of  tests  but  is  available  through  reference  laboratories is
            especially of the ileum, may also impede and blunt peak   plasma ammonia concentration. Fasting plasma ammonia
            absorption of the test meal. It is likely that fat content of the   can be measured in any cat or dog with historic or physical
            test meal is important because fat is the primary stimulus for   examination findings suggestive of HE. Signs of HE, whether
            the small intestinal mucosa to secrete cholecystokinin, which   they have a congenital or acquired basis, appear the same
            causes gallbladder contraction. Expulsion of bile during   (see Box 33.3). Quantifying the plasma ammonia concentra-
            periodic physiologic gallbladder contraction between meals   tion not only can confirm HE, although normal fasting
            may  complicate  interpretation  of  the  fasted  sample  result.   values in animals with hepatobiliary disease are relatively
            Lipemia of the sample can seriously affect the validity of the   common, but can also provide baseline data and help in
            test, particularly on heparinized blood. For this reason, it is   evaluating response to treatment. SBA values, particularly
            far preferable to use serum, both for the external samples   postprandial levels, provide similar information in dogs with
            and for the SNAP test. It is possible to use erythromycin at   congenital PSS. A high plasma ammonia concentration
            a small fraction of the therapeutic antibiotic dose (1-2.5 mg/  usually indicates reduced hepatic mass available to process
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