ADDITIONAL LABORATORY TESTING
Other specific laboratory tests may provide additional information about the nature and location of intestinal disease. In
some cases, a definitive diagnosis may be provided. Some of these tests are referred to as GI function tests. It is important
to point out, however, that many of the essential functions of the GI tract, such as secretion, motility, and immunologic
surveillance and protection, are not readily evaluated.
Folate (vitamin B9) is a water-soluble B-group vitamin. Serum folate concentrations are influenced by dietary intake, small intestinal brush
border enzyme activity, and the number and function of specific folate carriers in the proximal small intestine. Dietary deficiency
of folate is extremely uncommon, and low serum folate concentrations strongly suggest proximal small intestinal mucosal disease.10 Proper sample handling is important since hemolysis causes the release of folate from red blood cells, resulting in spuriously
high concentrations.
Cobalamin (vitamin B12) is also a water-soluble B-group vitamin. Only bacteria are capable of cobalamin synthesis, and cats are dependent on dietary
sources for their cobalamin needs. After ingestion, cobalamin is bound to salivary and gastric proteins and then transferred
to intrinsic factor in the duodenum. In cats, the exocrine pancreas is the only source of intrinsic factor. The cobalamin-intrinsic
factor complex then attaches to specific receptors in the ileum. As a result, subnormal serum cobalamin concentrations suggest
mucosal disease in the distal small intestine or exocrine pancreatic insufficiency (EPI).10
The trypsin-like immunoreactivity assay (TLI) determines serum trypsinogen and trypsin concentrations. Small amounts of these
enzymes can be found in the bloodstream after synthesis by the pancreatic acinar cells. Subnormal TLI concentrations are a
sensitive and specific marker for EPI.11 Administration of oral pancreatic extracts does not affect serum TLI concentrations. However, cats should be fasted for
12 hours before serum collection because patients with borderline exocrine pancreatic function may have results within the
normal range.
Additional testing for pancreatitis may be warranted in any cat with chronic signs of GI disease, especially if triaditis
complex—concurrent inflammation of the pancreas, hepatobiliary system, and GI tract—is suspected. The feline pancreatic lipase
immunoreactivity (fPLI) test has higher sensitivity and specificity when compared with abdominal ultrasonography for identifying
pancreatic inflammation, although the two tests may provide complementary information.12 Measuring serum amylase and lipase activities is no longer considered useful, and TLI concentrations are of limited value
for diagnosing feline pancreatitis.
ABDOMINAL IMAGING
Abdominal radiography in cats with chronic diarrhea is usually unrewarding but may indicate a foreign body, an obstruction,
an intussusception, a traumatic or congenital hernia, megacolon, or a mass lesion. An upper GI barium series may help to detect
motility disorders, bowel thickening, partial obstruction, bowel torsion or displacement, strictures, or masses. A barium
enema may be helpful to assess the large intestinal mucosa.
Abdominal ultrasonography is a more sensitive tool than radiography for detecting abdominal masses, intussusceptions, lymphadenopathy,
and intestinal wall thickening or loss of normal intestinal layering.13 Abnormal organ parenchyma, masses, and lymph nodes can be aspirated or biopsied with ultrasonographic guidance. Cytologic
examination of mesenteric lymph nodes cannot distinguish small cell lymphoma from normal lymph nodes. However, fungal disease,
mast cell disease, and large cell lymphoma can be reliably identified with cytologic evaluation of intestinal or lymph node
aspirates.
ENDOSCOPY
Depending on the results of the initial diagnostic tests, an endoscopic examination of the GI tract may be considered. This
test is relatively noninvasive but does have substantial limitations. Most important, not all of the intestine can be evaluated
since much of the small bowel is out of reach. An upper endoscopic examination permits visualization of the esophagus, stomach,
and proximal duodenum. The distal ileum may be reached via the colon during a lower endoscopic examination, but the jejunum
is inaccessible. In addition, only mucosal lesions can be identified, and focal thickening or submucosal changes will not
be appreciated. Thus, endoscopy is most appropriate in patients in which diffuse inflammatory or infiltrative mucosal disease
is suspected.
This diagnostic procedure requires specialized equipment and expertise. An inexperienced practitioner may have difficulty
entering the duodenum or ileum, and biopsy quality may be suboptimal.14 Multiple (six to 10) mucosal biopsy samples should be collected from the stomach, duodenum, ileum, and colon for histologic
examination, even if the tissue is grossly normal. Handle the samples carefully, and fix them quickly to avoid manipulation
artifact or drying.
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