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89 Cards in this Set

  • Front
  • Back
What diseases do Helicobacter pylori cause?
duodenitis, duodenal ulcers, type B chronic antral gastritis, gastric ulcers, nonulcer dyspepsia, gastric carcinoma, and MALTomas.
What is used for the diagnosis of Helicobacter pylori?
Tissue sampling, breath tests, and serology are used for diagnosis.
What is the underlying principle of the tests used for diagnosing Helicobacter pylori?
Testing utilizes the ability of the organism to produce urease (urease splits urea to form ammonia).
What stains can be used on tissue to confirm Helicobacter pylori?
Warthin-Starry or Giemsa’s stain.
What test confirms eradication of H. pylori after treatment?
Breath test.
What conditions suggest hypersecretory states of gastrin?
peptic acid disease in the absence of H. pylori or NSAID use. Failure to respond to H2-receptor blocking agents and PPIs are also suggestive.
What is the process of determining gastrin levels?
H2-receptor blockers should be held for 48 hours and PPIs for 7 days before testing.
Secretin can be given (2U/kg) with gastrin levels drawn at 2, 5, 10, 15, and 20 minutes.
What values give a positive gastrin test result?
An increase of more than 100 ng/L (normal <50 ng/L) is a positive result.
What laboratory values suggest a gastrinoma?
Serum gastrin levels greater than 150 ng/L (normal <100 ng/L) and pH levels <3.
What are the characteristics of chronic diarrhea?
more than 3 loose stools per day for more than 4 weeks or daily stool weight >200 g/day.
What are the types of chronic diarrhea?
Inflammatory diarrhea.
Secretory diarrhea.
Osmotic diarrhea.
Motility disorders.
What are the features of inflammatory diarrheas?
Often bloody with presence of leukocytes.
Examples include Crohn’s disease, ulcerative colitis, radiation colitis, ischemic colitis, and infectious colitis. Atypical inflammatory diarrheas such as collagenous colitis and microscopic colitis do not produce exudate but rather have hypersecretion or decreased absorption.
What are the features of secretory diarrheas?
Caused by active secretion of water that is greater than absorption capability.
Continues to create diarrhea even with fasting.
Can be caused by gastrinomas, carcinoid syndrome, VIP-producing carcinoma, mastocytosis, villous adenoma, and medullary thyroid carcinoma.
What does an osmotic gap <50 mOsm/kg in a patient with chronic diarrhea suggest?
that the patient has ingested a laxative causing secretory diarrhea such as sodium phosphate (Fleet phosphosoda).
What are the features of osmotic diarrheas?
Caused when the osmotic load of the fecal stream favors water loss (osmotic gradient drives water into lumen).
Fasting causes osmotic diarrheas to subside.
Magnesium laxatives (Maalox) can be responsible.
What osmotic gap value is associated with osmotic diarrhea?
Osmotic gap is characteristically >100 mOsm/kg. Stool MUST be fresh for calculating osmotic gap because fecal bacteria continues to produce osmotic particles.
Osmotic gap: 290- [2 x (Sodium+ Potassium)].
What is the formula to determine osmotic gap?
Osmotic gap: 290- [2 x (Sodium+ Potassium)].
What are the features of a motility disorder resulting in chronic diarrhea?
A diagnosis of exclusion.
Short gut syndrome decreases the amount of absorptive gut.
Irritable bowel syndrome can have excessive neural stimulation that decreases stool transit time.
What bacteria is seen with nosocomial diarrhea?
Clostridium difficile, a Gram-positive, spore-forming anaerobic bacillus.
What drugs have been implicated with the development of nosocomial diarrhea?
Broad-spectrum antibiotics such as clindamycin, penicillin, and cephalosporins.
What are the features of nosocomial diarrhea?
Presentation ranges from mild watery diarrhea to pseudomembranous colitis and toxic megacolon.
How is nosocomial diarrhea diagnosed?
C. difficile toxin A or B virulence factors in stool.
The gold standard is tissue culture cytotoxicity assays that detect cytotoxin B and takes 48 hours to complete.
Rapid enzyme immunoassays take only several hours but are not sensitive or specific.
ELISA is the optimal test in patients with >6 stools per day.
Stool culture takes 96 hours to complete.
What causes hepatic malabsorption?
obstruction of bile flow, which causes decreased fat absorption and decreased lipase activity.
What causes enteric malabsorption?
altered bacterial flora (blind loop syndrome, diverticulosis), obstruction of lymph flow, or enteritis.
Enteritis in the ileum results in B12 deficiency and decreased circulating bile acids.
What are the hallmarks of malabsorption?
Steatorrhea and fat-soluble vitamin deficiencies.
What is the definition of steatorrhea?
>5g of lipid in feces per 24 hours.
What is celiac sprue?
Intestinal malabsorption due to sensitivity to the alcohol-soluble portion of gliadin that induces nonspecific villous atrophy of the small intestine.
In what patient should celiac sprue be suspected?
A patient with iron deficiency anemia, weight loss, diarrhea, and bloating.
What conditions are associated with celiac sprue?
IgA deficiency, dermatitis herpetiformis, Down syndrome, type I diabetes, and autoimmune thyroid disease.
What abnormal cells are found in the peripheral blood of a patient with celiac sprue?
Target cells, Howell-Jolly bodies, Heinz bodies, and siderocytes.
What tests are used to diagnose celiac sprue?
Testing for antibodies to gliadin (AGA-IgA and AGA-IgG), endomysium (EMA-IgA), reticulin (ARA-IgA) and transglutaminase (tTG-IgG).
Which antibody has the greatest sensitivity and specificity for celiac sprue?
Endomysial antibodies.
What is the gold standard for the diagnosis of celaic sprue?
Flattened small bowel villi that respond to dietary changes.
What clinical sequelae are associated with Whipple disease?
Arthralgias, diarrhea, and weight loss.
What causes Whipple disease?
Tropheryma whippelii, a Gram-positive rod.
How is Whipple disease diagnosed?
PCR testing for infected tissue and CSF or biopsy of duodenum with PAS staining.
What is the treatment for Whipple disease?
Long-term antibiotic therapy with CNS penetration.
What is the significance of the Clinitest tablet?
It can be sued to test for disaccharidase deficiency.
Normal = 0.25 g/dL
Suspicious = 0.25-0.5 g/dL
Abnormal = >.5g/dL
What is the significance of perinuclear-antineutrophilic cytoplasmic antibody (pANCA) as it concerns inflammatory bowel disease?
It is found in 70% of ulcerative colitis patients and 20% of Crohn’s disease patients but rarely in irritable bowel syndrome.
What is the significance of anti-saccharomyces cerevisae (ASCA) as it concerns inflammatory bowel disease?
It is found in 65% of patients with Crohn’s disease and 20% of ulcerative colitis patients but rarely in irritable bowel syndrome.
What clinical sequelae are associated with carcinoid?
Abdominal pain, flushing, diarrhea, asthma, edema
What protein is elevated in carcinoid?
Serotonin.
What clinical sequelae are associated with gastrinoma?
Ulcers, diarrhea
What is gastrin?
A gastrointestinal hormone produced by antral G cells that regulates gastric acid secretion, stimulates gastric mucosa growth, increases blood flow to the stomach, and increases gastric and intestinal motility.
Originates from preprogastrin that is cleaved by trypsin to form gastrin.
What are the features of gastrin?
Optimal pH is 5-7, and a low pH has a negative-feedback mechanism.
Three forms: G34 (big gastrin), G17 (little gastrin), and G14 (mini gastrin).
What is the significance of measuring gastrin levels?
Used to diagnose suspected gastrin-secreting tumors (gastrinomas, Zollinger-Ellison syndrome).
How are gastrin levels measured?
Determined by RIA or ELISA.
Patient must fast 12 hours before testing because G34 doubles and G17 quadruples following a meal.
Specimen must be frozen immediately because gastrin is unstable in serum. 50% of its immunoreactivity is lost within 48 hours at 4ºC. Should be measured immediately after thawing.
What is the normal reference range of gastrin?
<100 ng/L, but gastrin increases with age.
In what conditions can elevated gastrin be seen?
gastric ulcer disease, hyperparathyroidism, chronic renal failure, short bowel syndrome, pernicious anemia, and vagotomy.
Why is gastrin measured during the removal of a gstrin-secreting tumor?
. If the entire specimen is removed, levels drop to within reference values within 20 minutes.
What gastrin level suggests the presence of a gastrinoma?
Gastrin > 1000 ng/L.
What gastrin level suggests Zollinger-Ellison syndrome.
Gastrin levels 2000 x normal.
What is pepsin?
An enzyme that hydrolyzes proteins to polypeptides.
What are the features of pepsin and pepsinogen?
Pepsinogen is activated by gastric acid to pepsin.
Pepsinogen I (PGI, pepsinogen A) and pepsinogen II (PGII, pepsinogen C) are stimulated by the vagus nerve, gastrin, secretin, and CCK and inhibited by gastric inhibitory peptide (GIP), vagotomy, H2-receptor antagonists, and anticholinergics.
At what pH are pepsinogens activated?
A low (acidic) pH.
At what pH are pepsinogens destroyed?
A high (alkaline) pH.
What is the ratio of PGI to PGII?
4:1.
With what conditions is elevated pepsinogen associated?
Diseases that cause increased gastric output such as gastrinomas, Zollinger-Ellison syndrome, gastritis, and duodenal ulcer disease.
Wit what conditions is decreased pepsinogen associated?
Atrophic gastritis and gastric carcinoma.
What is an Apt test?
It is a test used to determine if the blood in the GI tract of a newborn is from the infant or the mother.
How is the Apt test performed?
Stool sample is mixed with water, centrifuged, and the pink supernatant is mixed with 1% sodium hydroxide in a 5:1 ratio.
Turns yellow-brown if of maternal origin and remains pink if of fetal origin. Results occur due to HbF being more resistant to alkali denaturation.
What is the significance of measuring carotenoids in stool?
Carotenoids are the major precursor for vitamin A, a fat-soluble vitamin (depends upon presence of fat for absorption).
What conditions can cause low serum carotenoid?
Steatorrhea, liver disease, and high fever.
What conditions can cause elevated serum carotenoids?
Hypothyroidism, diabetes, hyperlipidemia, and excessive intake of carotene.
What is the significance of the breath test concerning the diagnosis of steatorrhea?
Based on measurement of 14CO2 in expired air following labeled triglycerides (triolein, tripalmitin, and trioctanoin).
Steatorrhea results in a decreased expired CO2, corresponding to decreased absorption of triglycerides.
How is a pancreatic cause of steatorrhea distinguished from other causes of steatorrhea using the breath test?
A two-stage test is used in which the patient is given labeled triglycerides in the first stage and the patient is given labeled triglycerides and pancreatic enzymes in the second stage.
What tests are used to diagnose steatorrhea?
Carotenoids, breath test, fecal fat, titrimetric method
How is fecal fat determination performed?
Patient must be placed on 100 g fat diet in adults.
In children, fecal fat determination is based upon percent coefficient of fat retention.
Coefficient of fat retention = [(Dietary fat-Fecal fat)]/Dietary fat) x 100.
<95% is indicative of steatorrhea.
What test is used for the definitive diagnosis of steatorrhea?
Fecal fat determination.
What are the limitations of fecal fat determination?
Measurement from wet weight concentration is the least informative, measurement from dry weight concentration is slightly more informative, and measurement from 24 hours is the most informative.
How is the titrimetric method of fat determination performed?
Fats and fatty acids are converted to soap through boiling of the feces with addition of alcoholic potassium hydroxide.
After cooling, hydrochloric acid is added to convert the soaps to fatty acids, which are then extracted with petroleum ether.
Calculated as fatty acids titrated with sodium hydroxide.
What is the D-xylose test?
A test for malabsorption.
How is a D-xylose test perrformed?
Patient is given a 25g dose of pentose sugar in 250g water administered orally, and the amount excreted in urine over 5 hours is measured.
<3g excreted is enterogenous malabsorption because pancreatic enzymes are not required for absorption of D-xylose.
Rate of absorption also depends on rate of excretion so a blood sample should be collected in patients with renal insufficiency 2 hours after administration of xylose.
What does clay colored stool suggest?
Absence of bile or presence of barium sulfate.
What are the characteristics of stool from a patient with steatorrhea?
Large amounts of soft, foul-smelling, gray stool.
What causes black stool?
Bismuth, iron, charcoal, and upper GI bleed.
What causes green stool?
Spinach, calomel, biliverdin, oral antibiotics.
What does translucent mucus in stool suggest?
spastic constipation or mucous colitis.
What does bloody mucus in stool suggest?
Neoplasm or inflammatory process.
What does mucus with pus in stool suggest?
Inflammatory process.
How is fat in stool visualized microscopically?
Sudan or Oil Red O stain by placing a small amount of stool on a slide and adding two drops of 95% ethanol, then two drops of saturated ethanolic solution of Sudan III.
Neutral fats appear as large orange-red droplets whereas fatty acids can appear as lightly stained flakes or unstained needle-like crystals.
If results are unequivocal, repeat the procedure adding several drops of 36% acetic acid and warming the mixture until it starts to boil.
This process converts fats and soaps to fatty acids.
Up to 100 stained droplets per HPF is normal.
How are meat fibers visualized microscopically in stool?
Stool is mixed with 10% alcohol solution of eosin for 3 minutes, and only rectangular fibers with cross-striation are counted.
How are leukocytes visualized microscopically in stool?
Mucus or a drop of liquid stool is placed on a slide and Loffler methylene blue is added. A differential count of at least 200 cells is made.
Why is fecal occult blood testing performed?
Decreases mortality from colon cancer by 15-35%.
What are the features of the Guiac fecal occult blood test?
Guiac is a phenolic compound that oxidizes quinone by hydrogen peroxide causing a color change.
Can detect presence of >20 mL/day blood in stool.
Need 3 consecutive stool samples.
Drugs that cause GI irritation (anticoagulants, aspirin, NSAIDs, colchicines, iron) can cause false-positives.
Ingestion of large amounts of vitamin C can cause a false-negative.
What are the features of the HemeSelect fecal occult blood test?
HemeSelect is an antigen-antibody reaction that does not react with nonhuman hemoglobin or peroxidase, unlike guiac. Also more specific for lower GI bleed because it targets the portion of hemoglobin that does not survive passage in the upper GI tract.
How is a lactose tolerance test performed?
The patient has to fast overnight and receives 50 g of lactose in 400 mL of water.
Blood is drawn at 30, 60, and 120 minutes after ingestion for testing. An optional 5-hour stool sample can be collected.
What lactose tolerance test value is associated with lactose tolerance?
Patients with deficiency have a rise <20mg/dL in glucose.
How much lactose is given to a child when performing a lactose tolerance test?
The dose of lactose in children is 2g/kg.