LAISHA
Open Laisha

EBVS European College diplomas Clinical, Diagnostic & Immuno-Parasitology: practice questions

EBVS European College diplomas (e.g. DipECVS, DipECVIM-CA) · Europe · European Board of Veterinary Specialisation and the individual colleges

Original practice questions written to the published syllabus · not past papers
10worked here, free
15written to this exam in this subject
8syllabus units

About EBVS European College diplomas

EBVS European College diplomas (e.g. DipECVS, DipECVIM-CA) is a specialist certification exam run by European Board of Veterinary Specialisation and the individual colleges, for candidates in Europe. College-specific: residency and exam.

Source: ecvd.org.

Checked against the exam body's published information. Formats and fees change; confirm the current edition there before you book.

Clinical, Diagnostic & Immuno-Parasitology in EBVS European College diplomas

The laboratory and field methods that find parasites in faeces, blood and skin, the immune response to parasites, parasitic zoonoses and integrated control. Advanced and postgraduate level.

Our 15 EBVS European College diplomas questions in this subject: 0 easy, 1 medium, 14 hard, across 8 units.

10 practice questions, worked

Choose an answer, then open the working. Each explanation says why the right answer is right and why the others are not.

These 10 were written to EBVS European College diplomas and are not shown on any other exam's page.

Question 1 · medium

A flotation device reads two chambers of 1 mL each from a suspension of 5 g of faeces made up to 50 mL. What is its analytical sensitivity (EPG represented by one egg)?

  1. 5 EPG
  2. 50 EPG
  3. 10 EPG
  4. 4.5 EPG
Answer and working

A. 5 EPG

Factor = 50 mL ÷ 2 mL read ÷ 5 g = 5 EPG per egg. 10 EPG would apply if only one chamber were read; 50 EPG is the usual McMaster factor; 4.5 EPG uses the 45 mL of added fluid instead of the 50 mL total.

Question 2 · hard

A practice offers flock monitoring by composite faecal egg count (equal weights from ten lambs pooled). Which statement about composite counts is correct?

  1. They give each lamb's count once the pooled result is divided by ten
  2. They are invalid for any resistance testing because the pooling step destroys strongyle eggs
  3. They estimate the group mean well but cannot show which individuals are high shedders
  4. They are less accurate than one individual count because pooling dilutes the eggs
Answer and working

C. They estimate the group mean well but cannot show which individuals are high shedders

Pooling equal weights gives an estimate of the mean at lower cost, but information on distribution between animals is lost. It does not destroy eggs, and the pooled result is a mean, not ten individual counts.

Question 3 · hard

A coprophagic dog's flotation shows large numbers of Eimeria oocysts and some strongyle-type eggs. The dog is healthy. The most likely explanation is:

  1. Pseudoparasites such as pollen grains and mites
  2. Spurious parasitism
  3. Canine coccidiosis caused by Eimeria species
  4. Ancylostoma infection with coccidial co-infection
Answer and working

B. Spurious parasitism

Eimeria does not infect dogs (canine coccidia are Cystoisospora); oocysts and strongyle eggs of herbivores pass through coprophagic dogs unchanged. Pseudoparasites are objects that only resemble parasite stages, whereas these are genuine parasite stages of another host. The spurious parasitism here comes from eating herbivore faeces.

Question 4 · hard

A flock has itchy sheep but surface scrapings are negative. Which additional test can detect Psoroptes ovis infestation at flock level, even early in infestation?

  1. A McMaster count of faecal mite eggs from ten ewes
  2. A modified Knott's test on pooled jugular blood
  3. An ELISA for serum antibodies against Psoroptes ovis
  4. A Giemsa smear of wool fibres from the shoulder area
Answer and working

C. An ELISA for serum antibodies against Psoroptes ovis

A serological ELISA detects antibodies to P. ovis and is used as a flock test in some countries, including before obvious lesions. Mite eggs are not counted in faeces, and Knott's test detects microfilariae.

Question 5 · hard

A test has sensitivity 90% and specificity 95%. It is used where 10% of animals are infected. What is the positive predictive value?

  1. 99%
  2. 95%
  3. 67%
  4. 90%
Answer and working

C. 67%

Per 1,000 animals: 100 infected give 90 true positives; 900 uninfected give 45 false positives. PPV = 90 ÷ 135 = 67%. 90% is the sensitivity, 95% the specificity, and 99% is close to the negative predictive value (855 ÷ 865).

Question 6 · hard

A serosurvey finds 25% of animals positive with a test of sensitivity 80% and specificity 95%. Using the Rogan–Gladen estimator, the true prevalence is about:

  1. 31.3%
  2. 25.0%
  3. 20.0%
  4. 26.7%
Answer and working

D. 26.7%

True prevalence = (AP + Sp − 1) ÷ (Se + Sp − 1) = (0.25 + 0.95 − 1) ÷ (0.80 + 0.95 − 1) = 0.20 ÷ 0.75 = 26.7%. 25% is the uncorrected apparent prevalence; 20% multiplies AP by Se; 31.3% divides AP by Se only, ignoring false positives.

Question 7 · hard

Two independent tests with sensitivities 80% and 70% are used in parallel (an animal is positive if either test is positive). The combined sensitivity is:

  1. 56%
  2. 150%
  3. 94%
  4. 75%
Answer and working

C. 94%

In parallel, an infected animal is missed only if both tests miss it: 0.2 × 0.3 = 0.06, so sensitivity = 94%. 56% (0.8 × 0.7) is the combined sensitivity of serial testing; 75% is a simple average; 150% adds them.

Question 8 · hard

Which factor is NOT a recognised reason why vaccines against parasites have been slow to develop?

  1. Parasites have too few antigens for the immune system to recognise
  2. Cheap, broad-spectrum antiparasitic drugs set a high commercial bar
  3. Parasites have multiple life stages expressing different antigens
  4. Many parasites actively evade or modulate host immune responses
Answer and working

A. Parasites have too few antigens for the immune system to recognise

Parasites have many antigens; the problem is finding protective ones. Multiple life stages, immune evasion and competition from cheap drugs are the real obstacles.

Question 9 · hard

Ten treated lambs have post-treatment counts (EPG) of 0, 0, 50, 0, 100, 0, 0, 50, 0, 0; the untreated control mean is 400 EPG. Using arithmetic means, what is the FECR?

  1. 95%
  2. 83%
  3. 50%
  4. 5%
Answer and working

A. 95%

Treated mean = 200 ÷ 10 = 20 EPG. FECR = 100 × (1 − 20 ÷ 400) = 95%. 5% is the fraction remaining; 83% averages only the three positive lambs (200 ÷ 3 = 66.7 EPG); 50% uses the group total of 200 instead of the mean.

Question 10 · hard

Demodex mites are found in deep scrapings from an adult dog that has developed generalised demodicosis for the first time at 8 years of age. What is the most important next step besides treating the mites?

  1. Treat all in-contact dogs, as adult-onset demodicosis is contagious
  2. Look for underlying disease or immunosuppressive treatment
  3. Stop investigating, as Demodex is never found in normal dogs
  4. Test the owners, as Demodex canis is a major zoonosis
Answer and working

B. Look for underlying disease or immunosuppressive treatment

Demodex canis is a normal follicular inhabitant; generalised disease starting in adulthood suggests failing immunity from endocrine disease, neoplasia or immunosuppressive drugs. It is not zoonotic or contagious between adult dogs.

A study plan for Clinical, Diagnostic & Immuno-Parasitology in EBVS European College diplomas

This plan follows where our questions actually fall, so the time goes where the marks are likely to be. It is our reading of the syllabus, not the exam body's weighting.

  1. First, the heavy units (60% of the 15 questions): Serodiagnosis of parasitic infections (5, 33%); Faecal egg counting: the McMaster method (2, 13%); Integrated parasite control (2, 13%).

    Read the manual chapters for these first and do every worked question you can find on them.

  2. Then the middle band: Skin scrapings (2, 13%); Anti-parasitic vaccines (1, 7%); Immunoparasitology (1, 7%).

    Aim for one sitting per unit, then mixed questions across them.

  3. Then the lighter units: Parasitic zoonoses (1, 7%); Sedimentation and flotation techniques (1, 7%).

    Learn the definitions, classifications and standard numbers; these units are more often recalled than worked.

  4. Leave time for the hard ones: Serodiagnosis of parasitic infections (5 hard of 5), Integrated parasite control (2 hard of 2), Skin scrapings (2 hard of 2).

    Come back to these after a first pass, untimed, and read every explanation, including for the options you rejected.

  5. Finish timed. Sit the subject as a timed set without notes, mark it, and send each wrong answer back to its unit above.

Last updated · How Laisha writes and checks its pages · Report a mistake

Ask Laisha about this

Opens Laisha's chat with your question ready to send. Sign in or start free.

Unlock every question — EBVS European College diplomas Clinical, Diagnostic & Immuno-Parasitology

US$10 a month · one price worldwide · cancel any time

  • Every practice question in this subject, with full working
  • Timed exam papers and progress by unit
  • Ask Laisha to explain any answer — up to 1,000 questions a month
Free or Smarter
FreeSmarter
Grow guides, pest pages, articlesRead allRead all
Ask Laisha5 a dayUp to 1,000 a month
Exam practiceThe sample on each pageEvery question, timed papers
Crop calendar and pest alerts—For your own fields
Calculators and tools—All
Uploads and reports—100 a month, real files
10 days free for every new account, no card.