Faecal analysis - lab session Flashcards

1
Q

What is the purpose of faecal analysis?

A

Allow us to identify:
- endoparasites and their eggs
- gastrointestinal disease
- digestive function
- diagnose bacteria/viral GI infections

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2
Q

What factors can effect the diagnostic quality of a faecal sample?

A

freshness of sample
amount
drying
contamination

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3
Q

What crude analysis of faeces can be performed?

A

smell
colour
consistency
presence of mucus
presence of worms

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4
Q

Different faecal collection methods? how should we store and preserve samples?

A

Can be collected rectally or as a fresh stool sample (<2 hours old)

Sample tube - fill to top - aim for 3-5grams
or clean plastic container

Label with animal’s details, date and place of collection

Can be kept up to three weeks in a fridge until processing – up to 2 months for parasites

Can add 10% formalin and keep it indefinitely
- not suitable for culture and may damage protozoa

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5
Q

What is a pooled sample? why do we do it?

A

Taking 3 separate samples across 3 days

Reduces the risk of a false negative or missing bacterial/ parasitic egg shedding.

Also reduced the chance of false positives due to contamination.

Faecal samples can be stored in the fridge between collections.

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6
Q

what are the different types of faecal testing?

A

McMaster Technique
Centrifugal flotation
Passive flotation
Baermann

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7
Q

How do you perform a passive flotation test?

A

Place faecal material into a disposable container

Add chemical solution

Macerate and mix gently

Add further chemical solution to dilute

Add sufficient to produce a rounded meniscus

Place a coverslip over the top

Leave for 15-20 mins

Remove the coverslip and place it on microscope slide

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8
Q

Positive and negatives of passive flotation?

A

Positive
- Less equipment
- Minimal steps

Negative
- Not as reliable - fecal debris may cover eggs
- longer time

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9
Q

How do you perform a centrifuge flotation?

A

Place fecal material into centrifuge tube

Add small amount of chemical solution

Macerate and mix gently

Add further chemical solution to dilute
- Add sufficient to produce a rounded meniscus

Place a coverslip over the top

Place into centrifuge
- Ensure to balance with the same tube and solution

Centrifuge for 3-5 minutes at 1000-1500RPM

Remove coverslip and place on microscope slide

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10
Q

Positives and negatives of centrifuge flotation?

A

Positives
- Reduces time by not waiting for passive flotation
- Increases yield of parasitic eggs

Negatives
- Requires more equipment

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11
Q

Advantages and disadvantages of faecal flotation?

A

Advantages
- Fast results
- Easy to obtain solutions
- Equipment easy to maintain

Disadvantages
- Can have contaminants from the environment - pollen, grass etc
- Can ‘miss’ or get false negative due to varying shedding of parasites
- Coprophagy (eaten faeces from another animal) may lead to false positives
- Some eggs may not float to the top and attach to the coverslip - false negative

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12
Q

What can you diagnose with floatation tests?

A

Roundworms
Hookworms
Whipworms
Giardia
Toxoplasmosis
Coccidia

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13
Q

How do you perform the McMasters technique?

A

Place 4g of fecal material and 56ml of chemical solution into measuring cyclinder

Macerate and mix gently

Using a sieve strain into a beaker
- keep liquid and dscard of solid waste

Leave faecal liquid for 5 mins

Place a small amount of the sample into a double-chambered microscopic slide

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14
Q

How do you analyse a McMaster’s sample under microcope?

A

Use 10x lens

Count the number of eggs within the grid of each chamber
- ignore all outside the squares

Multiply the total by 50
- this gives the eggs per gram of faeces

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15
Q

How do you perform the Baermann technique?

A

Place 5-10 grams of faeces on cloth
- tie four corners and apply an elastic band
- thread stick though to suspend on top of funnel

Fill funnel with lukewarm water to cover the sample
- leave to stand for 24hrs.

Take the bottom few mls,
- leave to stand for 30 mins
-or centrifuge for 2 mins at 1000 rpm

Remove sediment into petri dish
- some large nematodes may be seen.

Remove sediment from petri dish
- Place on slide
- Add drop of iodine and place cover slip

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16
Q

how does the Baermann technique work?

A

Works off active migration

Larvae move into the water and sink to the bottom

can then be collected for identification