Stool Analysis
Stool Analysis
Stool Analysis
Stool analysis is a series of tests done on a stool (feces) sample to help diagnose certain conditions
affecting the digestive tract . These conditions can include infection (such as from parasites, viruses,
or bacteria), poor nutrient absorption, or cancer.
For a stool analysis,
1.A stool sample (more than 2 gm) is collected in a clean container and then sent to the laboratory.
2. Laboratory analysis includes microscopic examination, chemical tests, and microbiologic tests.
3.The stool will be checked for color, consistency, shape, odor, and the presence of mucus. The stool may
be examined for hidden (occult) blood, fat, meat fibers,white blood cells, and sugars called reducing
substances. The pH of the stool also may be measured.
Why It Is Done: Stool analysis is done to:
Check for poor absorption of nutrients by the digestive tract (malabsorption syndrome).
Physical Examination:
a) Consistency and form: Normally faeces when passed tens to be well
formed and smooth.
1.Hard: If faces appear hard they might indicate constipation.
2.Flattened and ribbon like : stool indicate some obstruction in the
lumen of the bowel.
3.Semi-solid: In mild diarrhoea, digestive upsets, or after taking laxatives.
administration.
Chemical Examination
a)pH:
Normal stools are slightly acidic, slightly alkaline or neutral. The pH values range from 6.5 to 7.5.
1.
Strongly acidic stool (pH below 6.5) indicates an excess of carbohydrates in the diet.( It is
nonpathologic),and lactose intolerance. (It is pathologic).
2.
Strongly alkaline stool (pH above 7.5) indicates an excess of protein in the diet. It is non
pathologic.
3.
Occult blood: Generally it is not present. If there, it indicates either infection or some disorder
of the digestive system.
b)Reducing substances: They are generally found in stools of infants suffering from diarrhea . Faecal
Reducing Substances is a test to diagnose lactose intolerance (and some rare metabolic
abnormalities). Lactose intolerance can be caused by a prolonged or severe episode of viral
gastroenteritis. Other conditions, in which other sugars, such as glucose, sucrose and fructose are
not absorbed properly, can also cause a positive test for reducing sugars in the stool.
Reducing Substances are reported as:
Negative this is the normal result and means that the body is digestying and absorbing sugars
properly
Positive this means there are substances in the stool that can act as reducing agents, i.e.
there are forms of sugar in the stool that have not been absorbed by the body.
c)Fat: The fecal fat test measures the amount of fat in the stool ,that the body does not absorb. This test
evaluates fat absorption to tell how well the liver, gallbladder, pancreas, and intestines are
working.Fat malabsorption can cause a change in your stools called steatorrhea. To absorb fat
normally, the body needs bile from the gallbladder (or liver if the gallbladder has been removed),
enzymes from the pancreas, and normal intestines. This test evaluates fat absorption to tell how well
the liver, gallbladder, pancreas, and intestines are working.
Normal value:Less than 7 grams of fat per 24 hours.
MICROSCOPIC EXAMINATION :
Requirements: Stool sample,Saline/Iodine,toothpick.slides,coverslip,pH
indicator paper
Procedure:
Wet mount:Place a loopful of stool (or a small quantity with the help of
toothpick) on a slide and mix with a drop ofsaline/iodine until smooth. Cover
with a cover slip. Examine under 10x and 40x objectives. Report the
2.Epithelial Cells
Normally a few are present. If many are present, however, it indicates inflammation of the bowels.
3.Macrophages: Large mononuclear phagocytes with nucleus and ingested WBCs.
Normally, present only occasionally.If many are present, it indicates bacillary dysentery or ulcerative
colitis.
4.Eosinophil: may be present in allergies.
5.Erythrocytes (Red Blood Cells)
Normally absent. If present, it indicates lesions in the colon, rectum or the anus. If clumped, it means
amoebiasis (a kind of infective dysentery).
Note:Cells are usually reported as the number seen per high power field.
b) Crystals: Phosphates, oxalate, Calcium carbonate, Calcium sulphate,
Charcot Leyden crystals.
~Triple phosphate crystals are normal constituents of faeces and occur
as coffin lid shaped crystals
~.Calcium oxalate crystals, occur most frequently when fruits and
vegetables rich in oxalates are eaten.
Other Findings
1.
2.
Bacteria: Normally gram negative are present.If a high percentage of gram positive bacteria are
present, it indicates intestinal ulceration.
e) Intestinal Protozoa/Parasite: Iodine colors the egg and larvae and help in easy visulazation
of trophozoites also.
Note:Parasitic amoebae, eggs, larvae and cysts are usually reported as the
number seen in the entire preparation as follows.
Scanty (rare) 1-3, 3-10 (+), 10 to 20 (++), 20 to 40 (+++), and more
than 40 (++++).
Pathogenic:
.
Entamoeba histolytica cysts or vegetative form.
Giardia lambliacysts.
Balantidium coli:
:Left fig:Cyst
Right.fig:Trophozoite.
Nematohelminths
They are pathogenic in nature.e.g
Ascaris lumbricoides (roundworm).
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3.Identify a person who may not have any symptoms of disease but who carries bacteria that can spread
infection to others. This person is called a carrier. A person who is a carrier and who handles food is likely
to infect others.
Procedure:
1.Sterile the wireloop to red hot.Stab loop in areas where there is mucus,pus or
blood.
2.Streak on EMB and SS agar.
3.If Cholera is suspected,.inoculate a TCBS plate.
4.Incubate the plates for 24 hr at 37C.
5.Next day observre the colonies.If there are colorless colonies,inoculate them
on TSI for further investigation.
6.Next day observe TSI also.
7.Set up sensitivity in Mueller hinton plates by making lawn from EMB and SS
agar plates.
8.Incubate at 37C for 24 hr.
9.Next day not zones of inhibitions.