Sealed and sent to the laboratory immediately after collection
Preserved specimens can usually be kept at a room temperature
Large gallon containers for 24-, 48-, and72-hour stool collections for fecal fat and urobilinogen; specimens normally refrigerated throughout collection period
Carefully give instruction to the patient on how to properly collect their stool
Let the feces go on the side of the toilet and use the scooper to collect a pea-sized amount [avoid contamination with water]
Adult worms (ascaris, tapeworms), proglottids (egg laying segments of adult tapeworms), and parasitic indications (pus and mucus)
Samples containing adult worms (ascaris, tapeworms [thinner]) may be carefully washed through a wire screen. This process allows for the retrieval and examination of the parasites for identification purposes
CHEMICAL EXAMINATION
Detection of occult blood (hidden blood)
— Fat, urobilinogen (gives stool normal color) could be tested as well, not just occult blood
Hema-screen Guiac Slide Test Kit
Hema-screen slide
Hema-screen developer (<6% H2O2)
Results
(+) any trace of blue coloration
(-) no detectable blue coloration
INTERFERENCE OF FOBT : False-positive
Aspirin and anti-inflammatory medications
Red meat (beef or goat)
Horseradish
Raw broccoli, cauliflower, radishes, turnips
Melons
Menstrual and hemorrhoid contamination
INTERFERENCE OF FOBT : False-negative
Vitamin C > 250 mg/d
Iron supplements containing vitamin C
Failure to wait specified time after sample is
applied to add the developer reagent
MICROSCOPIC EXAMINATION
To detect the presence of parasites in a stool specimen
It can also reveal artifact (microscopic structures that can be seen in the stool)
It should be performed on a fresh specimen
NOPS – No ova and/or parasite seen
NIPS – No intestinal parasite seem
DIRECT FECAL SMEAR
About 2 mg of stool (amount forming a low cone at the tip of an applicator stick)
0.85% sodium chloride solution (NSS)
Cover with cover slip - Primary useful in the detection of motile protozoan trophozoites (pale and transparent)
Weak iodine solution (Lugol’s and D’Antoni) are temporary stain to demonstrate nuclei [help color the nuclei]
Helminth eggs and larvae can be detected using this preparation