Clinical Parasitology: Specimen Collection and Processing

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Flashcards covering specimen collection protocols, storage, preservation methods, macroscopic/microscopic examination, and specialized parasitologic techniques based on the MTY1206 Clinical Parasitology lecture.

Last updated 7:51 AM on 7/20/26
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34 Terms

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Definitive diagnosis

The demonstration of parasite or parasite components such as adults, egg, larvae, cysts, oocysts, trophozoites, and antigen.

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Presumptive evidence

The detection of the host immune response (antibodies) to the parasites.

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Typical stool collection protocol

Submission of 33 specimens, with one collected every other day for 1010 days.

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Amoebiasis collection protocol

Submission of 66 specimens within a period of 1414 days.

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Standard stool specimen size

A thumb-sized specimen for formed stool or 565-6 tablespoons for watery stool.

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Temporary storage temperature

Fecal samples should be stored in a 353-5℃ refrigerator; they must never be frozen or incubated.

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Stool to fixative ratio

One part stool to 33 parts preservative.

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5% Formalin

An all-purpose fixative concentration used specifically for protozoan cysts.

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10% Formalin

An all-purpose fixative concentration used for helminth eggs and larvae.

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Polyvinyl Alcohol (PVA)

A plastic resin incorporated into Schaudinn’s solution that serves to adhere stool onto a slide.

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Mercuric Chloride

A toxic substance contained in Schaudinn’s solution and PVA-based fixatives.

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Sodium Acetate-Acetic Acid Formalin (SAF)

A liquid fixative with a long shelf-life that does not contain Mercuric chloride.

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Liquid or soft consistency

Stool consistency associated with trophozoites that must be processed within 30mins30\,mins.

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Formed consistency

Stool consistency associated with cysts that should be processed within 34hrs3-4\,hrs.

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Dark red stool

Macroscopic observation indicative of upper GI bleeding.

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Bright red stool

Macroscopic observation indicative of distal location bleeding.

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Blood-tinged mucus (formed)

Macroscopic finding indicating the presence of trophic amoebae.

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Bloody mucus (loose/liquid)

Macroscopic finding indicating amoebic ulcerations.

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Charcot-Leyden Crystal

A specific microscopic finding in stool examination, often associated with immune response to parasites.

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Direct Fecal Smear (DFS)

A technique using small amounts of unfixed stool and Saline/Iodine for the detection of trophic forms of amoeba and flagellates.

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Iodine-stained Preparation

A preparation using Lugol’s or D’Antoni Iodine that kills trophozoites but enhances protozoan cysts.

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Glycerine

The reagent used as a clearing solution in the Kato Thick Smear.

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Malachite green

A reagent used in the Kato Thick Smear to minimize brightness.

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Concentration Techniques

Procedures used in light infections to recover cysts, oocysts, helminth eggs, and larvae based on specific gravity.

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40% HCl

A reagent in AECT used to dissolve albuminous material.

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Ether

A reagent used in AECT and FECT to dissolve neutral fat.

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Zinc Flotation Technique

A technique using 33%33\% Zinc Sulfate solution with an ideal specific gravity of 1.181.18 to 1.201.20.

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Sheather’s Sugar Flotation Technique

A method using boiled sugar solution and Phenol; it is best for the recovery of Coccidian oocysts like Cryptosporidium.

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Harada Mori

A test tube culture method used for hookworms, Strongyloides, and Trichostrongylus spp.

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Kato-Katz Method

An egg counting procedure used to assess the intensity of infection or worm burden.

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Perianal Swab

A collection method involving cellophane tape used to recover eggs of Enterobius vermicularis and Taenia spp.

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Knott’s conc. technique

A specialized technique used primarily for examining blood specimens.

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Xenodiagnosis

An advanced parasitologic technique listed for detecting specific infections.

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Enterotest

A specialized technique used for the recovery of parasites from the intestinal tract.