Past papers 5 Flashcards

1
Q

OSPACE example questions

Examine this Quality Control Chart (6 min)
a. What abnormality is shown in this quality control chart?
b. Which rule has been violated and how?
c. Give two possible scenarios which may account for this abnormality.

A

Westgard rules

Abnormality -
change in quality control batch
inappropriate storage of quality controls - temperature
inadequate maintenance of instrument
calibration errors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

OSPACE example questions

Examine these electron-micrographs (6 min)
a. In which clinical specimen type can you find all these viruses?
b. Name the viruses labelled A to G.
c. Which of these viruses belong to the same viral family? Name the family.
d. Which of these viruses have effective vaccines? What is t
he nature of this
vaccine?

A

Examine all EM pictures

A. Faeces
B. EM - 7 viruses. Possibly 5x GI viruses, plus CMV/ EBV
C. Caliciviridae - Noro/ Sapo
D. Rotavirus - live attenuated oral vaccine, children 8/12 weeks.
Adenovirus has live vaccine against types 4/7 - this is orally adminsitered. Only uses for military USA. Only for respiratory infections

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

OSPACE example questions

Examine this phylogenetic tree (6 min)
a. Does this phylogenetic tree support transmission of hepatitis C in the
dialysis unit? Why do you say so and which patients were involved?
b. Can you determine which patient is th
e index case from this tree? Why do
you say so?
c. What is the meaning of the number at the node of each branch?

A

Read phylogenetic tree flashcards

Nodes at each branch - the number is usually between 0 and 1.
A high value means that there is strong evidence that the sequences to the right of the node are correct

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

OSPACE example questions

These pictures are from different patients suffering different
complications of the same viral infection (6 min)
a. Which virus caused these complications?
b. Name each complication.
c. Name four other possible complications of this viral infection?

A

Not sure

Adenovirus?

conjunctivitis
Encpehalitis
Pneumonitis
Hepatitis
Gastroenteritis
Haemorrhagic cystitis

Enterovirus
Haemorrhagic conjunctivitisis
Meningitis
Myocarditis
Hand foot and mouth
Herpangina

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

OSPACE example questions

This is the histological examination of brain tissue of a man died of an unexplained encephalopathy (6 min)

a. What is the diagnosis?
b. What is the pathognomonic feature found in the histology slide?
c. How do you diagnose this condition before death?

A

? HSV encephalitis

necrosis of medial temporal lobe/ frontal lobe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

OSPACE example questions

This is the brain MRI of a patient from sub-Saharan Africa who
presented with a two week history of headache and admitted with generalised seizures (6 min)

a. What is the most likely diagnosis?
b. Name one possible alternative diagnosis.
c. What is the most likely underlying condition?
d. What is the management of this condition?

A

HIV

?cysticercosis - most common cause seizures worldwide. Pork tapeworm

Toxoplasma
Malignancy e.g Lymphoma
Viral encephalitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

OSPACE example questions

8.
Examine these clinical pictures (6 min)
a. Which two viral infections were demonstrated in these clinical pictures?
b. Name the signs found in the oral cavity and match each one to its
corresponding clinical picture.
c. What laboratory methods are available to diagnose these two infections?

A

?EBV - oral hairy leukoplakia
PCR and histology + IHC

?HHV8 - Kaposi sarcoma
PCR and histology + IHC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

OSPACE example questions

Examine these monolayer cell culture inoculated with respiratory
sample from a patient (6 min)

a. Describe the morphology of the cells.
b. Describe the cytopathic effect observed
c. What viruses could be growing in this cell monolayer with this cytopathic effect?

A

?RSV

cytopathic effect -
enlarged multinucleated cells with cytoplasmic inclusions - syncytium

syncytium infection -
RSV
Covid
HSV
VZV
EBV
CMV
HIV

typically enveloped viruses that cause cell fusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

OSPACE example questions

Examine this HIV protease and reverse transcriptase sequence and
the report? (10 min)
a. What mutations are shown?
b. What are the clinical significances?
c. Recommend a suitable treatment regimen for this patient

A

Learn common mutations

Learn which drugs to switch to

probably switch:
2x NRTI + PI to
2x NRTI + INT

Probably switch NNRTI to NRTI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

OSPACE example questions

A nucleic acid amplification test for Chlamydia trachomatis
has a claimed sensitivity of 99.9% and a specificity of 99.9% for self-
taken vulvo-vaginal swab in women (7 minutes)

It is applied to two different populations, screening 10,000 individuals in each group:

Population A:
Sexually active female teenagers (prevalence 1 in 100)
Population B:
Asymptomatic women > 40 years old (prevalence 1 in 1000)

A 2x2 table has been completed for population A

Test pos: 100 TP /1 TN aka false pos Total: 101
Test neg: 0 TP aka false neg / 899 TN Total: 899
Total: 100 TP / 900 TN Total: 1000

Draw out 2x2 table

What is the PPV for the test in population A?

A

The positive predictive value is the probability that following a positive test result, that individual will truly have that specific disease.

PPV = TP/ TP + FP

PPV = 100 TP/ 100 TP + 1 FP

PPV = 100/ 101 = 99%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

OSPACE example questions

A nucleic acid amplification test for Chlamydia trachomatis
has a claimed sensitivity of 99.9% and a specificity of 99.9% for self-
taken vulvo-vaginal swab in women (7 minutes)

It is applied to two different populations, screening 10,000 individuals in each group:

Population A:
Sexually active female teenagers (prevalence 1 in 100)
Population B:
Asymptomatic women > 40 years old (prevalence 1 in 1000)

A 2x2 table has been completed for population A

Test pos: 100 TP /1 TN aka false pos Total: 101
Test neg: 0 TP aka false neg / 899 TN Total: 899
Total: 100 TP / 900 TN Total: 1000

Draw out 2x2 table

What is the NPV for the test in population A?

A

The negative predictive value is the probability that following a negative test result, that individual will truly not have that specific disease.

NPV = TN/ TN + FN

NPV = 899 TN/ 899 + 0 FN

NPV = 100%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

OSPACE example questions

A nucleic acid amplification test for Chlamydia trachomatis
has a claimed sensitivity of 99.9% and a specificity of 99.9% for self-
taken vulvo-vaginal swab in women (7 minutes)

It is applied to two different populations, screening 10,000 individuals in each group:

Population A:
Sexually active female teenagers (prevalence 1 in 100)
Population B:
Asymptomatic women > 40 years old (prevalence 1 in 1000)

A 2x2 table has been completed for population A

Test pos: 100 TP /1 TN aka false pos Total: 101
Test neg: 0 TP aka false neg / 899 TN Total: 899
Total: 100 TP / 900 TN Total: 1000

Draw out 2x2 table

Calculate the same table for population B

A
  1. Sensitivity is the ability to detect the true positives ie not falsely assigning them to false neg (C), specificity is the ability to detect the true negatives, if neither of these are 100% then you may get some false negatives and false positives.
  2. Positive predictive value is likelihood that positive test = true positive ie A/(A+B)x100.
  3. If the prevalence of infection is 1 in 1000 then in 10,000 there should be 10 true positives. If the sensitivity is 99.9% then if you test those 10 true positives you will be right 99.9% of the time, 0.1% of 10 is so small that 0 goes in C. So I think all of the true positives will be detected and correctly assigned to A.
  4. If the prevalence is 1 in 1000 then in 10,000 there should be 9990 true negatives. If specificity is 99.9%, then you will be wrong 0.1% of the time. 0.1% of 9990 is 10. So I think that 9980 of your 9990 will be correctly assigned as negative and 10 will be incorrectly assigned as positive (B).
    I reckon the PPV is therefore 10/20x100 = 50%.

True pos/ Test pos 10 (A)
True pos/ Test neg 0 (C)
True neg/ Test pos 10 (B)
True neg/ Test neg 9980 (D)

Test pos total - 20
Test neg total - 9980

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

OSPACE example questions

Explain the difference between positive predictive values between populations between A + B

A

For any given test (i.e. sensitivity and specificity remain the same) as prevalence decreases, the PPV decreases because there will be more false positives for every true positive. This is because you’re hunting for a “needle in a haystack” and likely to find lots of other things that look similar along the way – the bigger the haystack, the more frequently you mistake things for a needle.

Therefore, as prevalence decreases, the NPV increases because there will be more true negatives for every false negative. This is because a false negative would mean that a person actually has the disease, which is unlikely because the disease is rare (low prevalence).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

OSPACE example questions

You are asked to set up a multiplex real time PCR for influenza viruses.

1.1.List the basic reagents required in a real time PCR reaction.

A

PCR

6 main components:

DNA template
primers
nucleotides
enzymes - DNA polymerase (Taq polymerase) or reverse transcriptase
reaction buffer - magnesium
fluorescent probes for real-time PCR - e.g SYBR green

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

OSPACE example questions

You are asked to set up a multiplex real time PCR for influenza viruses.

1.2.Explain the mechanism of action of a dual-labelled probe in real time PCR.

A

Dual labeled probes used in quantitative real-time PCR systems take advantage of the 5’ -> 3’ exonuclease activity of Taq polymerase.

Dual labeled probes contain a 5’ fluorescent reporter and a 3’ quencher which anneals between the PCR primers.

During the extension phase of PCR, the 5’ -> 3’ exonuclease activity of Taq polymerase cleaves the fluorescent reporter from the probe. The amount of free reporter accumulates as the number of PCR cycles increases.

The resulting, detectable fluorescence signal is proportional to the amount of accumulated PCR product - this provides real-time analysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

OSPACE example questions

You are asked to set up a multiplex real time PCR for influenza viruses.

1.3. What is SYBR Green and how can it be used in a PCR designed to
detect two viral variants?

A

SYBR green binds to dsDNA, and fluoresces, allowing measurement of PCR product

viral variants - have different DNA/RNA sequences. So will have different melt curves, and different fluorescent pattern e.g may see a double peak in melt curve

17
Q

OSPACE example questions

A multiplex real time PCR run for influenza A and influenza B matrix
targets and an internal control target is performed and the amplification curves are provided.
The run include throat/nasal swabs from the following 4 patients:

Patient A/Sample A – 52 year old man with lymphoma who has just
completed chemotherapy and found to be in remission. Admitted to
hospital with fever, cough and shortness of breath.
Chest x-ray showed patchy consolidation.

Amplification Plots:

Analyse the results and provide a report for each sample. Please
explain any anomalies.

What further tests would you recommend on each sample?

Provide management advice to the clinical team in each case

A

Reject run as negative control is positive - suggets contamination. Cannot exclude a positive result is due to contamination. However, may want to act on positive results e.g start oseltamivir for influenza, if clinical picture/ radiology compatible

Influenza including typing
Covid
Adenovirus
Enterovirus
Parainfluenza

CMV/ EBV

HSV/ VZV/ Adeno PCR blood

PCP

bacterial/ fungal culture

Management -
oseltamivir/ zanamavir if high risk resistance
IPC - Side room respiratory precautions

answer unclear

18
Q

OSPACE example questions

A multiplex real time PCR run for influenza A and influenza B matrix
targets and an internal control target is performed and the amplification curves are provided.
The run include throat/nasal swabs from the following 4 patients:

Patient B/Sample B – 20 year old international student returned from
China 2 days ago. Admitted to hospital with fever and flu like
symptoms. ? atypical pneumonia.

Amplification Plots:

Analyse the results and provide a report for each sample. Please
explain any anomalies.

What further tests would you recommend on each sample?

Provide management advice to the clinical team in each case

A

Reject run as negative control is positive - suggets contamination. Cannot exclude a positive result is due to contamination. However, may want to act on positive results e.g start oseltamivir for influenza, if clinical picture/ radiology compatible

Avian influenza
Covid
SARS
MERS

HIV
Hendra/ Nipah
Leptospirosis
Legionella

Management
Side room with respiratory precautions

answer unclear

19
Q

OSPACE example questions

A multiplex real time PCR run for influenza A and influenza B matrix
targets and an internal control target is performed and the amplification curves are provided.
The run include throat/nasal swabs from the following 4 patients:

Patient C/Sample C– 63 year old woman returned 2 days ago from a
pilgrimage to Saudi Arabia. Developed high fever and was admitted to ITU with respiratory distress.

Amplification Plots:

Analyse the results and provide a report for each sample. Please
explain any anomalies.

What further tests would you recommend on each sample?

Provide management advice to the clinical team in each case

A

Reject run as negative control is positive - suggets contamination. Cannot exclude a positive result is due to contamination. However, may want to act on positive results e.g start oseltamivir for influenza, if clinical picture/ radiology compatible

Covid
MERS

Management
Side room with full PPE as could be MERS

answer unclear

20
Q

OSPACE example questions

A multiplex real time PCR run for influenza A and influenza B matrix
targets and an internal control target is performed and the amplification curves are provided.
The run include throat/nasal swabs from the following 4 patients:

Patient D/Sample D – 4 year old boy previously healthy. Attended GP
because of coryzal symptoms. Up to date with immunisation.

Amplification Plots:

Analyse the results and provide a report for each sample. Please
explain any anomalies.

What further tests would you recommend on each sample?

Provide management advice to the clinical team in each case

A

Reject run as negative control is positive - suggets contamination. Cannot exclude a positive result is due to contamination. However, may want to act on positive results e.g start oseltamivir for influenza, if clinical picture/ radiology compatible

check he has not had recent intranasal immunisation

management -
if no admission required, symptomatic treatment

answer unclear

21
Q

How many HIV tests are required to confirm a diagnosis?

A

3 separate tests

2x serology/ antigen tests
1x tests to discern HIV1 from HIV2

22
Q

First HIV1/2 serology test positive
Second HIV1/2 serology test positive
HIV1 p24 antigen negative

HIV immunoblot is indeterminate

What is the most likely diagnosis?

A

HIV2 infection

Some shared proteins, can flag weak pos on immunoblot

Or maternal transferred antibodies

23
Q

HIV Geenius immunochromatographic test

Which proteins detect HIV1?

A

p24
p31
gp 41
gp 160

gp 160 made from gp120 external glycoprotein, and gp41 transmembrane protein

HIV2 also has p31 sometimes

24
Q

HIV Geenius immunochromatographic test

Which proteins detect HIV2?

A

gp 36 transmembrane protein
gp 140

25
Q

Suspected HIV2 positive on screening tests

What further specific tests in relation to this pathogen would you advise?

A

HIV2 viral load
HIV2 proviral DNA

History of travel/ links to West Africa. But also France/ Portugal which have west Africa links

26
Q

New HIV diagnosis

List all the baseline pathogen-
based laboratory investigations on blood
samples for a patient with a new diagnosis of this infection [use precise pathogen-target scientific terminologies]

A

Repeat confirmation of result
HIV avidity
HIV RNA PCR viral load
HIV proviral DNA PCR

CD4 count
U&Es
LFTs
Bone profile
HLA B27

HBsAg
Anti-HBc
Anti-HCV

Syphilis IgG screening
Chlamydia/ Gonorrhoea NAT

Toxoplasma
Stronglyoides
CrAg serum

27
Q

HIV2

What classes of antivirals are contraindicated?

A

NNRTI due to reverse transcriptase binding site change

Enfuvirtide fusion inhibitor also contra-indicated

28
Q

HIV2

name three NRTI drugs where there is evidence of efficacy?

A

Tenofovir alafenamide/ disoproxil
Emtricitabine
Abacavir
Lamivudine

Tenofovir + emtricitabine is first line backbone

Abacavir + lamivudine is second line backbone if cant have other drugs

29
Q

HIV2

in addition to NRTI, name three classes of drug where there is evidence of efficacy

A

Integrase strand transfer inhibitors

Protease inhibitors

Maraviroc entry inhibitor - in vitro activity shows efficacy, but not used in practice