INDIVIDUAL TESTS *Indicates send out test I NDIVIDUALTESTS CODE TEST DESCRIPTION *S16005 ACETYLCHOLINE RECEPTOR ANTIBODY Specimen: 1mlserum, preferred sample Method: Immunoprecipitation RIA Schedule: 7-14 working days Indication: Diagnosis of acquired Myasthenia gravis. Interpretive Guidelines: Apositive titerconfirms a diagnosis ofMyasthenia gravis. Negativetiterscanoccur in 10 to 20% ofcases, therefore, a negative result does notexclude Myasthenia gravis. T435 ACTH ( Endogenous level ) Specimen: Plasmafrom LT containing aprotinin. Method: RIA Schedule: 7working days Indication: Todifferentiate pituitary-dependentfrom adrenaltumor hyperadrenocorticism. Interpretive Guidelines: Endogenous ACTH concentrations will be increased ( > 45 pg/ml ) in approximately 90% of dogs with PDH and will be decreased ( < 15 pg/ml ) in approximately 60% of dogs with adrenal tumor hyperadrenocorticism. A value between 15 and 45 pg/ml is non-diagnostic. Comments: UseLTcontainingaprotinin for sample collection, centrifuge immediately and transfer plasma to a plastic vial. ( Antech will provide the necessary tubes. ) Transport on ice or cold packs. Do not use any plain, uncoated glass tubes or pipettes. Please allow for a minimum of three daystoobtain the special containerfrom oursupply department. 23 “Defining the Standard of Excellence” Rev.April 2007 INDIVIDUAL TESTS *Indicates send out test I NDIVIDUALTESTS CODE TEST DESCRIPTION T440 ACTH RESPONSE TEST ( CORTISOL 2 ) Specimen: 1 ml serum or heparinized plasma per tube, label tubes PRE and POST Method: RIA Schedule: Daily ( M-Sat ) Indication: Investigation of hypoadrenocorticism or hyperadrenocorticism. Monitoring response to Lysodren or Trilostane treatment. Special Drawing instructions: Canine(using Acthar ACTH gel ): 1) Collect pre-sample; label tube "Pre-ACTH." 2) Inject 2.2 IU/kg ( maximum 40 units ) ACTH gel IM. 3) Collect 2 hr post-sample; label "2 hr Post ACTH." Canine(using synthetic ACTH ): 1) Collect pre-sample; label tube "Pre-ACTH." 2) Inject 0.25 mg Cosyntropin ( Cortrosyn ) IM or IV OR inject 5 ug/kg IV only. 3) Collect 1 hr post-sample; label "1 hr Post ACTH." Feline ( using Acthar ACTH gel ): 1) Collect pre-sample; label tube "Pre-ACTH." 2) Inject 2.2 IU/kg ACTH gel IM. 3) Collect 1hr and 2 hr post-samples; label accordingly. Feline ( using synthetic ACTH ): 1) Collect pre-sample; label tube "Pre-ACTH." 2) Inject 0.125 mg Cosyntropin ( Cortrosyn ) IM or IV. 3) Collect 1 hr post sample; label accordingly. Equine: 1) Draw a resting cortisol. Centrifuge tube, remove the serum and refrigerate. 2) Inject ACTHgel: 0.5I.U. per pound givenIMorsyntheticACTHgelmay be used 100 I.U. given IV or IM. 3) Collect a 4 hr post sample if using the ACTH gel. Collect a 2 hr post sample if cosyntropin is given IV. Collect a 2 & 4 hr post sample if cosyntropin is given IM. Centrifuge the tube, remove the serum and refrigerate. Comments: If animal is on Prednisone, wait 24 hours before doing test. If animal has received Methyl Prednisone acetate, wait 6 weeks before drawing. Dexamethasone will not interfere with cortisol assay, other than suppressing the pre value. 24 “Defining the Standard of Excellence” INDIVIDUAL TESTS *Indicates send out test I NDIVIDUAL TESTS CODE TEST DESCRIPTION T010 ALBUMIN Specimen: 1 ml serum, heparinized or EDTA plasma Method: Bromcresol Green dye Schedule: Daily Indication: To assess the quantity of this major protein which maintains colloid osmotic pressure and acts as a carrier protein for many other compounds. Interpretive Guidelines: Decreased with renal or intestinal disease ( increased loss ), or hepatic disease ( decreased production ). Increase seen only with hemoconcentration due to dehydration. Comments: 1) Hypoalbuminemia may result in edema/ascites. 2) Hypoalbuminemia may result in a decrease of any compound carried by albumin ( e.g. Calcium ) T215 ALK PHOS ISOENZYME ( Canine only ) ` Specimen: 1 ml serum Method: Heat inactivation or Levamisole inhibition Schedule: 1 - 2 working days Indication: Measures corticosteriod induced fraction of alkaline phosphatase. Interpretive Guidelines: Increased with corticosteroids, Cushing’s or persistent stress. 25 “Defining the Standard of Excellence” Rev.April 2007 INDIVIDUAL TESTS *Indicates send out test I NDIVIDUAL TESTS C T D ODE EST ESCRIPTION T020 ALKALINE PHOSPHATASE Specimen: 1 ml serum or heparinized plasma Method: Kinetic/Bowers&McComb Schedule: Daily Indication: Evaluation of hepatic disease ( esp. the biliary system ), hyperadrenocorticism, and less commonly, bone disorders. Interpretive Guidelines: Increased with cholestasis, any condition resulting in increased osteoblastic activity ( e.g. fracture repair, bone neoplasms ), phenobarbital or phenytoin medication, and corticosteroid excess. Comments: 1) Young animals will often show an increase secondary to normal bone growth. 2) In canines ONLY, there is a steroid-induced fraction ( Cushing’s, steroid therapy ), which can be differentiated from the hepatic fraction by special testing ( heat resistance test, levamisole inhibition test ). T030 ALT ( SGPT ) Specimen: 1 ml serum or heparinized plasma Method: Kinetic/Wroblewski & LaDue Schedule: Daily Indication: Evaluation of hepatic disease. Interpretive Guidelines: Increase in this cytosolic enzyme indicates cell membrane damage and leakage, secondary hepatic infection, inflammation, trauma, neoplasia, anoxia/hypoxia, and hepatoxic compounds ( including a variety of drugs ). Comments: 1) Value does not necessarily correlate with the degree of hepatic insufficiency. 2) A moderate increase may be induced by glucocorticoids or anti-convulsant medication. 3) Severe muscle damage may cause ALT to increase. 26 “Defining the Standard of Excellence” INDIVIDUAL TESTS *Indicates send out test I NDIVIDUAL TESTS CODE TEST DESCRIPTION T040 AMYLASE Specimen: 1 ml serum or heparinized plasma Method: Kinetic/CNPG3 substrate Schedule: Daily Indication: Evaluation of pancreatic disease. Interpretive Guidelines: Increases are seen with pancreatitis, azotemia, and, less commonly, intestinal disease and hepatic disease. Comments: 1) Value may not correlate with the severity of pancreatic disease. 2) Amylase is cleared through the kidney; therefore, the value is affected by the glomerular filtration rate. T050 AMYLASE and LIPASE Specimen: 1 ml serum or heparinized plasma Method: Please refer to individual tests Schedule: Daily Indication: Pancreatic disease panel. *S16872 ANAPLASMA PHAGOCYTOPHILUM TITER ( Canine and Equine only ) Formally called Ehrlichia equi Specimen: 1 ml serum Method: IFA Schedule: 2 - 4 working days Indication: Investigation of granulocytic ehrlichiosis. Interpretive Guidelines: May infect various species; positive results indicate previous or current infection. Increasing titers seen in recent infections. Comments: This organism was formally called Ehrlichia equi. 27 “Defining the Standard of Excellence” Rev.April 2007 INDIVIDUAL TESTS *Indicates send out test I NDIVIDUAL TESTS C T D ODE EST ESCRIPTION *S16265 ANAPLASMA PLATYS TITER Formally called Ehrlichia platys Specimen: 1 ml serum Method: IFA Schedule: 5 - 7 working days Indication: Check for exposure to A. platys in cases of cyclic thrombocytopenia. Interpretive Guidelines: Positive results indicate exposure to A. platys. Comments: This organism was formally called Ehrlichia platys. T515 ANTINUCLEAR ANTIBODIES ( ANA ) Specimen: 1 ml serum Method: IFA Schedule: 1 - 2 working days Indication: Evaluation for Systemic Lupus Erythematosus ( SLE ) in patients with appropriate history, clinical and laboratory findings. Interpretive Guidelines: The ANA titer is a sensitive but not specific test for SLE. Elevated ANA titers can occur in other inflammatory diseases, although these titers tend to be low. Comments: False negative results can occur from long-term glucocorticoid administration. *S16055 ARSENIC Specimen: 1 ml heparinized plasma or LT 1 ml urine or 0.5-1 gram kidney or liver tissue or 10 grams stomach content, feed or water SHIP ON ICE Method: Atomic absorption Schedule: 7 - 10 working days Indication: Suspicion of arsenic toxicity. Interpretive Guidelines: Levels above baseline are consistent with Arsenic toxicity. 28 “Defining the Standard of Excellence” INDIVIDUAL TESTS I *Indicates send out test NDIVIDUAL TESTS C T D ODE EST ESCRIPTION T060 AST ( SGOT ) Specimen: 1 ml serum or heparinized plasma Method: Kinetic/Enzymatic Schedule: Daily Indication: Evaluation of hepatic and muscle disease. Interpretive Guidelines: Increase in this enzyme indicates hepatic cell damage ( infection, inflammation, neoplasia, trauma, anoxia/hypoxia, hepatotoxic compounds ), or muscle disease ( inflammation, infection, necrosis, trauma, anoxia/hypoxia, neoplasia ). Comments: 1) Hemolysis may interfere with result. 2) AST is a mitochondrial enzyme, therefore, an increase reflects more serious cell damage. 3) AST is not as liver-specific as ALT; significant increases in both enzymes suggest the AST increase is of hepatic origin. *S16070 BABESIA CANIS TITER Specimen: 1 ml serum or plasma Method: IFA Schedule: 5 - 7 working days Indication: Detection of occult ( no visible parasitemia ) Babesia canis infections. Interpretive Guidelines: A positive titer indicates exposure to, and likely chronic infection with, Babesia canis. Dogs may be seropositive with no clinical signs of illness. *S16075 BABESIA GIBSONI TITER ( non export ) Specimen: 1 ml serum or plasma Method: IFA Schedule: 7 – 10 working days Indication: Detection of occult ( no visible parasitemia ) Babesia gibsoni infections. Interpretive Guidelines: A positive titer indicates exposure to, and likely chronic infection with, Babesia gibsoni. Dogs may be seropositive with no clinical signs of illness. Comments: When exporting use test code *S16502. 29 “Defining the Standard of Excellence” Rev.April 2007 INDIVIDUAL TESTS *Indicates send out test I NDIVIDUAL TESTS CODE TEST DESCRIPTION T785 BAERMANN FECAL Specimen: Feces Method: Baermann Schedule: 2 - 7 working days Indication: Concentration technique used to collect certain parasites in larval stages or as ova; most often used to detect larvae of respiratory nematodes. *S16001 BARTONELLA CULTURE ( Cat Scratch Fever ) Specimen: 2 ml LT. Send cold. Method: Culture Schedule: 4 weeks Indication: Investigates cats as carriers of Bartonella. Interpretive Guidelines: A positive culture result confirms that the cat is infected with Bartonella. The organism is present in the blood in low numbers so false negative results may occur. Therefore, a negative culture result does not exclude the cat as a carrier of Bartonella. Comments: Bartonella PCR testing and Bartonella serology are more sensitive tests for detecting carrier cats. *S85889 BARTONELLA HENSELAE TITER ( Feline only ) Specimen: 1 ml serum Method: ELISA Schedule: 5 - 12 working days Indication: Investigate cats as carriers of Bartonella. Comments: Additional testing for Bartonella include PCR testing and culture. 30 “Defining the Standard of Excellence” INDIVIDUAL TESTS *Indicates send out test I NDIVIDUAL TESTS C T D ODE EST ESCRIPTION *S1315 BARTONELLA PCR ( Cat Scratch Fever ) Specimen: 1 ml LT, Send cold. Method: PCR Schedule: 5 – 7 working days Indication: Investigate cats as carriers of Bartonella. Interpretive Guidelines: A positive test indicates active infection. False negative results may occur due to the low numbers of circulating organisms but PCR testing is more sensitive than culture. Comments: Bartonella serology can also be used to investigate Bartonella infection. T220 BILE ACIDS, PRE AND POST Specimen: 1 ml serum or heparinized plasma ( pre and post ) Method: Enzymatic Schedule: 1 - 2 working days Indication: Tests for hepatic insufficiency or portosystemic shunts. Interpretive Guidelines: 1) Elevated levels are seen with decreased hepatic function. 2) Steroid hepatopathies may cause mild to moderate elevations. 3) High levels may be seen with portosystemic shunts. Comments: Fast for 12 hours prior to drawing pre- sample. Feed a small fatty meal and draw post 2 hours later. Label tubes accordingly. Occasionally, fasting levels are greater than the post-prandial level. This occurrence may be due to spontaneous gall bladder contraction prior to feeding. T225 BILE ACIDS, RESTING Specimen: 1 ml serum or heparinized plasma Method: Enzymatic Schedule: 1 - 2 working days Indication: May be useful for portosystemic shunts, but pre/post test is recommended. Interpretive Guidelines: 1) Elevated levels are seen with decreased hepatic function. 2) Steroid hepatopathies may cause mild to moderate elevations. 3) High levels may be seen with portosystemic shunts. Comments: Fast for 12 hours prior to draw. Occasionally, fasting levels are greater than the post-prandial level. This occurrence may be due to spontaneous gall bladder contraction prior to feeding. 31 “Defining the Standard of Excellence” Rev.April 2007 INDIVIDUAL TESTS *Indicates send out test I NDIVIDUAL TESTS C T D ODE EST ESCRIPTION T070 BILIRUBIN, direct Specimen: 1 ml serum or heparinized plasma Method: Van den Bergh & Mueller Schedule: Daily Indication: Evaluation of liver and biliary diseases. Interpretive Guidelines: Increased levels are seen in biliary disease ( including both intrahepatic and extrahepatic lesions ) hepatocellular disease ( hepatitis, cirrhosis and advanced neoplastic states ) and hemolytic disease. T090 BILIRUBIN, total Specimen: 1 ml serum or heparinized plasma or LT Method: Colorimetric Schedule: Daily Indication: Liver disorders, post hepatic disease, hemolytic disorders. Interpretive Guidelines: Elevation may be due to pre-hepatic ( hemolytic ), intrahepatic ( inflammation, infection, or neoplasia ) or post-hepatic ( adhesion, swelling, neoplasia, etc.) causes. T520 BLADDER TUMOR antigen (Canine only) Specimen: 2 ml Urine in RT ( spin urine, submit supernatant ) Method: Latex agglutination Schedule: 1 - 2 working days Indication: As a screening test to investigate possible transitional cell carcinoma. Interpretive Guidelines: If the Bladder Tumor antigen ( BTA ) is negative, then transitional cell carcinoma is unlikely ( 90% sensitivity ). Significant pyuria or hematuria, however, may cause false positives ( 78% specificity ). Animals with positive results should be further evaluated ( ultrasound, radiographs, cytology, biopsy, etc. ) to confirm the presence of neoplasia. 32 “Defining the Standard of Excellence”
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