Animal Diagnostic Sàrl.

Analyses

Equine Analyses

Coprological analyses (parasites) are carried out according to several distinct techniques which make it possible to highlight the presence of parasites in their various forms (adult stages, larval stages, eggs).

We are, of course, willing to advise you on diagnostic issues beyond selective deworming, because even if you do not opt for a complex program, a coprological examination before deworming medication remains highly recommended.

We also offer all the necessary analyses for parasitic research associated with coprological analysis, such as cultures, DNA detection (PCR), IFAT, ELISA.


Material and Quantity:

  • The necessary materials and quantities are indicated below each analysis.
  • A sufficient quantity of faeces must be sent depending on the analyses (minimum 20 to 50 g) for equines. Do not forget to identify samples.
  • Sedimentation-Flotation and MacMaster sensitivity can be increased by taking coprological samples over several days (e.g. 1 sample taken over 3 consecutive days).

Corpological Analysis - Equines

- Nematodes, Cestodes, Coccidians oocysts, detection + egg count (EPG determination: Egg per Gram)
Quantity: 40 g / 2 dung balls min.

- Nematodes, Cestodes, Coccidians oocysts detection + egg count (EPG determination: Egg per Gram) + lungworms detection.

- A method which allows Nematode (Strongyles, Parascaris equorum) eggs excretion rate detection. Expressed in EPG (Egg per Gram).
Quantity: 20 g / 1-2 dung balls min.

- Nematodes, Cestodes and Coccidians oocysts parasite eggs detection. Method sensitivity can be increased by taking coprological samples over several days (e.g. 1 sample taken over 3 consecutive days).
Quantity: 40 g / 2 dung balls min.

- Due to resistance cases increase, it is recommended to carry out this resistance test 14-17 days post-treatments, to determine the FECRT.
Quantity: 20 g / 1-2 dung balls min

- Qualitative method for highlighting lungworms (Dictyocaulus arnfieldi). Infestation is rare in horses and occurs mainly when in contact with donkeys.
Quantity: 20 g / 1-2 dung balls min.

- On blade (adhesive) direct Oxyuris equi egg detection. To increase test sensitivity, repeat the scotch test over several days (2, 3 days).

- The culture is made from a positive coprological sample (Strongyles eggs presence). Used to differentiate larvae from small to large Strongyles.
Quantity: 50-100 g, taken over 3 days.

- Detection of small and large liver flukes.
Quantity: Since coprological excretion is not constant, it is important to take a coprological sample for several consecutive days (min 5 days).

The selective deworming program is based on regular analysis of coprological samples throughout the year.

These analyses provide an accurate overview of parasite egg excretion for each horse. Only animals with high egg excretion (> 200 EPG, or secretion of particular parasites) will be treated.

Selective deworming analyses are mainly performed with McMaster. However, it is strongly recommended to combine the analysis with Sedimentation-Flotation to increase test sensitivity.

You can find more information on selective deworming on our dedicated page.

Ruminants & New World Camelids

Bovines, Caprines and Ovines

Coprological analyses are carried out according to several distinct techniques which enables highlighting the presence of parasites in their various forms (adult stages, larval stages, eggs). Samples taken over 3 days allow an increase in tests sensitivity.

We also offer all the necessary analyses for parasitic research associated with coprological analyses, such as cultures, DNA detection (PCR), IFAT, ELISA.

Corpological Analysis -
Ruminants & New World Camelids

- Trematodes (Flukes, Paraphistomes) eggs, Cestodes eggs, Nematodes eggs, Coccidian oocysts. detection. Lungworms detection.
Quantity: 30-50 g min. fresh fecal matter.

- Trematodes (Flukes, Paraphistomes) eggs, Cestodes eggs, Nematodes eggs, Coccidian oocysts. detection.
Quantity: 30-50 g min. fresh fecal matter.

- Sedimentation (Flukes, Paraphistomes)
- Flotation (Cestodes eggs, Nematodes eggs, Coccidian oocysts)
- Baermann (lungworms detection)
Quantity: 20-30 g min. fresh fecal matter.

- A method which allows Nematodes eggs excretion rate detection. Expressed in EPG (Egg per Gram).
Quantity: 10-20 g min. fresh fecal matter.

- Due to resistance cases increase, it is recommended to carry out this resistance test 14-17 days post-treatments, to determine the FECRT.
Quantity: 10-20 g min. fresh fecal matter.

- The culture is made from a positive coprological sample (Strongyles eggs presence). Used to differentiate larvae from small to large Strongyles.
Quantity: 50-100 g taken over 3 days.

Dogs and Cats Analysis

It is important to regularly examine fecal samples from domestic animals to detect parasitic infestations, such as gastrointestinal worms, tapeworms, roundworms, Giardia and other protozoa.

Dewormers can then be administered in a more targeted manner and only when necessary, while preserving your pet and family’s health.

Lessening the use of deworming treatments helps to maintain their effectiveness by fighting the emergence of resistance, which currently is a real problem.

Analyses do not replace visits to the veterinarian, conversely it can guide the choice towards appropriate pest control.

Corpological Analysis - Cats and Dogs

Dogs, Cats, Small animals
Search for Cestodes eggs, Nematodes such as: Tapeworm, Ascarids (Toxocara), Ancylostoma.
Quantity: 1 whole nut equivalent, or 20-30 g. To increase test sensitivity, take a sample over three consecutive days.

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