Specimen Collection and Processing Flashcards

1
Q

the most common procedure performed in the area of parasitology is the examination of a stool specimen for _

A

ova and parasites (abbreviated as O&P)

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2
Q

ova refers to the _ stage of parasite

A

egg

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3
Q

When present, the protozoan forms known as _ may be recovered from these samples.

A

trophozoites and cysts

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4
Q

_ stages, such as eggs, larvae, proglottids, and adult worms, may also be found.

A

Helminth

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5
Q

The typical stool collection protocol con- sists of three specimens, one specimen collected every other day or a total of _ collected in _.

A

3; 10 days

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6
Q

Stool samples from patients whose therapy includes _ oil should be col- lected prior to therapy or not until 5 to 7 days after the completion of therapy.

A

barium, bismuth, or mineral

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7
Q

Collection of speci- mens from patients who have taken antibiotics or antimalarial medications should be delayed for _ following therapy.

A

2 weeks

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8
Q

Amount of stool required for parasite study

A

2-5 g; “walnut size”

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9
Q

t/f. Urine should not be allowed to con- taminate the stool specimen because it has been known to destroy some parasites.

A

true

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10
Q

Stool should not be retrieved from toilet bowl water because _ may be con- fused with human parasites.

A

free-living protozoa and nematodes

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11
Q

To demonstrate the motil- ity of protozoan trophozoites, a _ specimen is required.

A

fresh

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12
Q

liquid stool must be examined within _

A

30 minutes

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13
Q

usually found in liquid stool

A

trophozoites

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14
Q

semiformed specimen should be evaluated within

A

1 hour

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15
Q

usually seen in semiformed specimen

A

protozoan cysts and trophozoites

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16
Q

formed specimens can be held for _

A

24 hours

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17
Q

substances that preserve the morphology of protozoa and prevent further development of certain helminth eggs and larvae

A

fixatives

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18
Q

recommended part of fixative and stool

A

3:1

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19
Q

The specimen must be fixed in the preservative for at least _ minutes before processing begins.

A

30

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20
Q

all-purpose fixative for the recovery of protozoa and helminths

A

formalin

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21
Q

5% formalin concentration ideally preserves

A

protozoan cysts

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22
Q

10% formalin concentration ideally preserves

A

helminth eggs and larvae

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23
Q

does not preserve parasite morphology adequately for permanent smears (-)

A

formalin

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24
Q

a plastic powder that acts as an adhesive for the stool specimen when preparing slides for staining

A

polyvinyl alcohol

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25
PVA combined with Schaudinn solution has _ chloride base which can cause potential health problem.
mercuric
26
viable alternative to the use of PVA and Schaudinn fixative
SAF (sodium acetate formalin)
27
requires a single vial and it is mercury-free
SAF
28
SAF is easy to prepare, has a long shelf life, and can be used for preparing smears for staining with the modified acid-fast stain to detect _
coccidian oocysts
29
t/f SAF-preserved specimens is not as clear in permanent stains as when mercury-containing preservatives are used.
true
30
SAF for permanent stains with _ provide better results
iron hematoxylin
31
Other alternatives to mercury-based PVA are the use of sub- stitute compounds containing copper sulfate or zinc sulfate
modified polyvinyl alcohol
32
free of formalin and mercury and can be used for concentration techniques and permanent stained smears
alternative single-vial systems
33
Conspicuously fibrous
hard (dark brown)
34
Fiber scanty to moderate
soft (black)
35
colloidal (homogenous)
mushy (brown)
36
scanty mucus
loose (pale brown)
37
much mucus
diarrheic (clay)
38
mucus with scanty blood
watery, liquid (yellow)
39
formed stool color
red-brown
40
semiformed stool color
green, other
41
The microscopic examination of stool for ova and parasites involves three distinct procedures:
1. direct wet preparation 2. concentration technique 3. permanent staining
42
it is necessary for the microscope to contain a specially designed ocular piece equipped with a measuring scale known as
ocular micrometer
43
The ocular micrometer is a disk that is inserted into the _ of the micro- scope.
eyepiece
44
primary purpose is to detect the presence of motile protozoan trophozoites
direct wet preparation
45
added preservative in direct wet prep
saline or iodine
46
% of saline in direct wet prep
0.85%
47
A direct iodine wet preparation may be made to enhance the detail of protozoan _
cysts
48
to aggregate parasites present into a small volume of the sample and to remove as much debris as possible that might hinder the labora- tory technician’s ability to see any parasites present clearly
concentration techniques
49
2 types of concentration methods
- flotation - sedimentation
50
most widely used sedimentation technique that provides good recovery of most para- sites and is easy to perform
Formalin–Ethyl Acetate Sedimentation Procedure
51
it yields a cleaner preparation, making it easier for microscopic examination but some helminth eggs are very dense and will not float
Zinc Sulfate Flotation Technique
52
to confirm the presence of protozoa cysts and/or trophozoites by staining intracellular organelles
permanent stains
53
if a permanent stained smear is not performed, this parasite will likely be missed
Dientamoeba fragilis
54
Helminth eggs or larvae are best detected and identified using a
concentration technique
55
Two common stains used for routine O&P testing include
trichrome (Wheatley modifica- tion) and iron hematoxylin
56
most widely used stain with a relatively long shelf life and the procedure is easy to perform
wheatley trichrome
57
reveals excellent morphology of the intestinal protozoa
iron hematoxylin
58
A modified iron hematoxylin stain has been developed that incorporates a _ step; this allows for the detection of acid-fast parasites
carbol fuchsin
59
from which area can the Enterotest be used to collect specimens?
duodenum
60
how many hours Enterost incubates
4 hours
61
helpful for detecting E. histolytica
sigmoidoscopy material
62
for the detection of Enterobius vermicularis
cellophane tape prep
63
in cellophane tape prep, when does the specimen collected?
morning before the patient washes or defecates
64
If malaria is suspected, it is best to prepare smears within _ of collection.
1 hour
65
smear for frequently satisfactory screening purooses
thick smear
66
smear that provides best biew of the malarial parasite in the RBCs and recommended for species indentification
thin smears
67
two permanent stains commonly used
• Wright’s stain • Giemsa stain
68
preferred stain because it allows for the detection of parasite detail necessary for species identification
giemsa stain
69
to concentrate blood specimens sus- pected of containing low numbers of microfilariae
knott technique
70
knott technique consist of 1ml of blood and _ of _
10 mL of 2% formalin
71
specimen collected for the diagnosis of amebic conditions
Cerebrospinal fluid (CSF)
72
recommended for the recovery of a number of parasites, including intracellular organisms such as Leishmania spp. and T. gondii.
Tissue and biopsy specimens
73
sputum typically collected and tested from patients suspected of being infected by the lung fluke _
Paragonimus westermani
74
specimen for Acanthamoeba keratitis
eye specimen
75
is best diagnosed by the collection and examination of corneal scrapings.
Acanthamoeba keratitis
76
t/f. Mouth scrapings are the sample of choice for the detection of E. gingivalis and Trichomonas tenax, whereas nasal discharge specimens are helpful for the recovery of parasites such as N. fowleri.
true
77
Useful in the detection of Onchocerca volvulus
skin snips
78
a technique used for the diagnosis of Chagas’ disease
xenodiagnosis