Stool Studies



Stool Studies






OVERVIEW OF STOOL STUDIES

The elimination of digestive waste products from the body is essential to health. Excreted waste products are known as stool or feces. Stool examination is often done for evaluation of gastrointestinal (GI) disorders such as GI bleeding, GI obstruction, obstructive jaundice, parasitic disease, dysentery, ulcerative colitis, and increased fat excretion.

Stool is composed of the following materials:



  • Waste residue of indigestible material (e.g., cellulose) from food eaten during the previous 4 days


  • Bile (pigments and salts)


  • Intestinal secretions


  • Water and electrolytes


  • Epithelial cells that have been shed


  • Bacteria


  • Inorganic material, mainly calcium and phosphates


  • Undigested or unabsorbed food (normally present in very small quantities)

The output of feces depends on a complex series of absorptive, secretory, and fermentative processes. Normal function of the colon involves three physiologic processes: (1) absorption of fluid and electrolytes, (2) contractions that churn and expose the contents to the GI tract mucosa and transport the contents to the rectum, and (3) defecation.

The small intestine is approximately 23 feet (7 m) long, and the large intestine is 4 to 5 feet (1.2 to 1.5 m) long. The small intestine degrades ingested fats, proteins, and carbohydrates to absorbable units and then absorbs them. Pancreatic, gastric, and biliary secretions exert their effects on the GI contents to prepare this material for active mucosal transport. Other active substances absorbed in the small intestine include fat-soluble vitamins, iron, and calcium. Vitamin B12, after combining with intrinsic factors, is absorbed in the ileum. The small intestine also absorbs as much as 9.5 L of water and electrolytes for return to the bloodstream. Small intestine contents (i.e., chyme, which contains fragments of proteins, droplets of fat, salt, and water) begin to enter the rectum as soon as 2 to 3 hours after a meal, but the process is not complete until 6 to 9 hours after eating.

The large intestine performs less complex functions than the small intestine. The proximal, or right, colon absorbs most of the water remaining after the GI contents have passed through the small intestine. Colonic absorption of water, sodium, and chloride is a passive process. Fecal water excretion is only about 100 mL/day. The colon mainly moves the luminal contents by seemingly random contractions of circular smooth muscle. Increased propulsive activity (i.e., peristalsis) occurs after eating. Peristaltic waves are caused by the gastrocolic and duodenocolic reflexes, which are initiated after meals and stimulated by the emptying of the stomach into the duodenum. The muscles of the colon are innervated by the autonomic nervous system. In addition, the parasympathetic nervous system stimulates movement, and the sympathetic system inhibits movement. Massive peristalsis (progressive waves of muscular contractions pushing the contents ahead) usually occurs several times a day. Resultant distention of the rectum initiates the urge to defecate. In persons with normal motility and a mixed dietary intake, normal colon transit time is 24 to 48 hours.


STOOL ANALYSIS

Stool analysis determines the various properties of the stool for diagnostic purposes. Some of the more frequently ordered tests on feces include tests for leukocytes, blood, fat, ova, parasites, and pathogens (Table 4.1). (See Chapter 7 for stool culture.) Stool is also examined by chromatographic analysis for the presence of gallstones. The recovery of a gallstone (precipitated by cholesterol or bile pigments) from feces provides the only proof that a common bile duct stone has been dislodged and excreted. Stool analysis also screens for colon cancer and asymptomatic ulcerations or other masses of the GI tract and evaluates GI diseases in the presence of diarrhea or constipation. Stool analysis is done in immunocompromised persons for parasitic diseases. Fat analysis is used as the gold standard to diagnose malabsorption syndrome. The Centers for Disease Control and Prevention recommend that stool samples submitted for enteric pathogen testing should also be tested for Shiga toxin (produced by Escherichia coli O157:H7 and other strains of E. coli).









TABLE 4.1 Stool Testing for Infections




































Source of Stool Infection


Clinical Signs or Symptoms


Laboratory Test (Sequence or Follow-up)


Community Acquired from intermediate hosts, such as:


Diarrhea, bloody, purulent Steatorrhea


Cramping, bloating, belching


Small bowel obstruction, weight loss


Generalized skin rash


Huge swelling of legs, arms, or scrotum


Huge lymphatic swelling Fever, chills, night sweats


Screen stool for ova and parasites


Microscopic exam of stool for ova and parasites


Stool culture for Clostridium difficile (some patients may require more than one assay)


Eosinophilia in blood sample


Exam for worms in stool or around anus


Fecal smear for leukocytes and yeast



Home—domestic pets, contaminated water Occupational




Fishers—from snails and worms


Meat cutters—from contaminated animals


Healthcare workers— from patients


Farm workers—from animals (cows, pigs), garden, flies, mosquitoes, fleas, other insects



Recreational—backpacking, poor sanitation




Travel—Third World— contaminated water supply


Contact with fair animals



Hookworm infection—not fecal or oral; passed via direct penetration of skin by larva in contaminated soil or in animal droppings


Nosocomial Acquired from institutions such as hospitals or nursing homes


Diarrhea Medication history of antibiotic use


Eosinophilia in blood sample


Exam for worms in stool or around anus


Microscopic exam of stool for ova and parasites


Stool culture for C. difficile


Fecal smear for leukocytes and yeast


Personal Contact with an infected host when patient is compromised (weakened immune system; i.e., HIV) or debilitated (such as a frail child or elderly patient)


Testing may occur following contact with infected host but before symptoms appear.


Screen stool for ova and parasites


Microscopic exam of stool for ova and parasites


Stool culture for C. difficile Toxin stool assay


Acid-fast bacilli (AFB) in stool for tuberculosis


Microsporidium



Patients and healthcare personnel may dislike collecting and examining stool samples; however, this natural aversion must be overcome in light of the value of a stool examination for diagnosing disturbances and diseases of the GI tract, the liver, and the pancreas.


STOOL SPECIMEN COLLECTION AND TRANSPORT PROCEDURES


• Collection and Transport Procedures for All Types of Stool Collection



Interfering Factors



  • Stool specimens from patients receiving tetracyclines, antidiarrheal medications, barium, bismuth, oil, iron, or magnesium may not yield accurate results.


  • Bismuth found in paper towels and toilet tissue interferes with accurate results.


  • Do not collect or retrieve stool from the toilet bowl or use a specimen that has been contaminated with urine, water, or toilet bowl cleaner. A clean, dry bedpan may be the best receptacle for defecation.


  • Inaccurate test results may result if the sample is not representative of the entire stool evacuation.


  • Lifestyle, personal habits, travel, home and work environments, and bathroom accessibility are some of the factors that may interfere with proper sample procurement.


  • Prompt transport of the specimen is necessary for accurate results. Trophozoites (protozoa in the early growth stage) in liquid stool disintegrate rapidly after defecation; therefore, the specimen needs to be examined 30 minutes from start of collection of specimen, not 30 minutes from end of collection. Semi-formed stool should be examined within 60 minutes after defecation. No trophozoites are seen in formed stool.




• Collection and Transport of Random Specimens



  • Observe the Collection and Transport Procedures for All Types of Stool Collection on pages 276 through 277 of this chapter.


  • Collect the entire stool sample and transfer it to a clean container using a clean tongue blade or similar object. A sample 2.5-cm (1-inch) long or 64.7 mg (1 oz) of liquid stool may be sufficient for some tests.


  • For best results, cover specimens and deliver to the laboratory immediately after collection. Depending on the examination to be performed, the specimen should be either refrigerated or kept warm. Contact the laboratory for detailed instructions concerning the temperature of stool specimen before collection is begun to avoid delay once the specimen is obtained.


• Collection and Transport of Specimens for Ova and Parasites



  • Observe the Collection and Transport Procedures for All Types of Stool Collection on pages 276 through 277 of this chapter.


  • Warm stools are best for detection of ova and parasites. Do not refrigerate specimens for ova and parasites.



  • Special vials that contain 10% formalin and polyvinyl alcohol (PVA) fixative may be used for collecting stool samples to test for ova and parasites.


  • Because of the life cycle of parasites, three separate random stool specimens for analysis are recommended.


• Collection and Transport of Specimens for Enteric Pathogens



  • Observe the Collection and Transport Procedures for All Types of Stool Collection on pages 276 through 277 of this chapter.


  • Some coliform bacilli produce antibiotic substances that destroy enteric pathogens. Refrigerate the specimen immediately to prevent this from happening in the sample.


  • Samples that are diarrheal rather than formed stool are usually still adequate to give accurate results.


  • A freshly passed stool is the specimen of choice.


  • Collect stool specimens before antibiotic therapy is initiated and as early in the course of the disease as possible.


  • If mucus or blood is present, it should be included with the specimen because pathogens are more likely to be found in these substances. If only a small amount of stool is available, a walnut-sized specimen is usually adequate.


  • Keep the outside of the collection container free from contamination and immediately send the sealed container to the laboratory.


  • For best preservation and transport of specimens suspected of containing pathogens, a Cary-Blair solution (which contains sodium thioglycolate, disodium phosphate, sodium chloride, agar, and distilled water) vial with indicator should be used.


• Collection and Transport of 24-, 48-, 72-, and 96-Hour Stool Specimens

This method is used to test for fat, porphyrins, urobilinogen, nitrogen, and electrolytes.


Procedure for Submitting Individual Specimens



  • Observe the Collection and Transport Procedures for All Types of Stool Collection on pages 276 through 277 of this chapter.


  • Collect all stool specimens for 1 to 3 days. The entire stool should be collected. Some procedures may require 4 days.


  • Label specimens with day of test (e.g., Day 1, Day 2, Day 3, Day 4), time of day collected, patient’s name, and test(s) ordered. It is important to disclose the number of days collected because this information is needed for calculations.


  • Submit individual specimens to the laboratory as soon as they are collected.


Procedure for Submitting Total Specimens



  • Observe the Collection and Transport Procedures for All Types of Stool Collection on pages 276 through 277 of this chapter.


  • Obtain a 1-gallon container from the laboratory (a 1-gallon paint tin or covered plastic pail is preferred).


  • Save all stool and place in the container. Keep refrigerated or in a container with canned ice and replace ice as needed.


  • Label the specimen with the patient’s name, dates and times of collections, duration of collection time, and test(s) ordered.


  • Transfer the properly labeled container to the laboratory at the end of the collection period.



STOOL STUDIES


• Stool Consistency, Shape, Form, Amount, and Odor

Inspection of the feces is an important diagnostic tool. The quantity, form, consistency, and color of the stool should be noted. Normally, stool reflects the shape and caliber of the colonic lumen as well as the colonic motility. The normal consistency is somewhat plastic and neither fluid, mushy, nor hard. Consistency can also be described as formed, soft, mushy, frothy, or watery. When diarrhea is present, the stool is watery. Large amounts of mushy, frothy, foul-smelling stool are characteristic of steatorrhea (excess fat in the feces). Constipation is associated with hard, spherical masses of stool.

Feces have a characteristic odor that varies with diet and the pH of the stool. The odor of normal stool is caused by indole (produced in intestine by breakdown of tryptophan) and skatole (formed from decomposition of protein) formed by bacterial fermentation and putrefaction.


Normal Findings



  • 100 to 200 g/24 hours or 100 to 200 g/day


  • Characteristic odor present; plastic, soft, formed; soft and bulky on a high-fiber diet; small and dry on a high-protein diet; seeds and small amounts of vegetable fiber present (as opposed to muscle fiber) (Table 4.2)





• Stool Color

The brown color of normal stool is probably due to stercobilin (end product of heme catabolism), a bile pigment derivative, which results from the action of reducing bacteria in bilirubin and other undetermined factors.

The first indication of GI disturbances is often a change in the normal brown color of the feces. A change in color can provide information about pathologic conditions, organic dysfunction, or intake of drugs. Color abnormalities may aid the healthcare provider in selection of appropriate diagnostic chemical and microbiologic stool tests.


Normal Findings

Brown



Sep 25, 2018 | Posted by in PATHOLOGY & LABORATORY MEDICINE | Comments Off on Stool Studies
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