5 January 2023.
57 |
Role-play. Trans man |
58 |
SBA. Lynch syndrome. |
59 |
EMQ. Toxoplasmosis |
60 |
SBA. Quinolone antibiotics |
61 |
EMQ. Listeriosis and pregnancy |
57. Role-play.
Candidate’s instructions.
You are an ST5 doctor
in the gynaecology clinic, your next patient is Mr Vic Williams; you have
received the following letter from the GP. Take a history from the patient and
make a management plan.
Dear Doctor,
I should be most grateful if you would see Vic
Williams, a 35-year-old transgender man. He appears to have a premature
menopause and I have no idea about the implications. He was referred to the
gender identity clinic one year ago but the waiting list for a first appointment
is two years, so he is not yet on any hormone therapy. He has two children,
both by normal delivery before he decided to transition and was ‘Victoria’. The
children are 12 and 14 and seem well-adjusted to the maternal gender change.
Vic has no significant medical history. I shall be most grateful for your
expert opinion. Dr. P.E.R. Plexed.
58. SBA. Lynch syndrome.
Lynch syndrome.
Abbreviations
CRC: colorectal
cancer.
EC: endometrial
cancer.
IBD: inflammatory
bowel disease: Crohn’s & ulcerative colitis.
IDDM: insulin-dependent
diabetes mellitus.
Ls: Lynch
syndrome.
MLH: mutL-homolog
family of DNA, mismatch repair genes.
MMR: mismatch
repair.
MSH: mutS
homolog family of DNA, mismatch repair genes.
Question 1.
What is Lynch syndrome?
Option List
A |
auto-immune
condition leading to reduced factor X levels in blood |
B |
hereditary condition which increases the risk of many
cancers, particularly breast |
C |
hereditary
condition which increases the risk of many cancers, particularly breast &
colorectal |
D |
hereditary
condition which increases the risk of many cancers, particularly colorectal
& endometrial |
E |
none of
the above |
Question 2.
How is Lynch syndrome inherited?
Option List
A |
it is an
autosomal dominant condition |
B |
it is an autosomal recessive condition |
C |
it is an X-linked dominant condition |
D |
it is an X-linked recessive condition |
E |
none of the above |
Question 3.
Which, if any, of the following genes can cause Lynch syndrome?
Option List
A |
MLH1 +
MLH2 + MOH1 |
B |
MLH1 + MLH2 + MSH1 |
C |
MLH1 + MLH2 + MSH6 |
D |
MLH1 + MSH2 + MSH6 |
E |
None of the above |
Question 4.
Mutations of which 2 of the following genes cause most cases of Lynch
syndrome?
Option List
A |
MLH1 +
MLH2 |
B |
MLH1 + MSH1 |
C |
MLH1 + MSH2 |
D |
MLH2 + MSH1 |
E |
MLH2 + MSH2 |
Question 5.
What is the approximate prevalence of Ls in the UK population?
Option List
A |
1 in 50 |
B |
1 in 100 |
C |
1 in
1,000 |
D |
3 in
1,000 |
E |
none of the above |
Question 6.
Approximately what % of individuals with Ls have had the diagnosis
established?
Option List
A |
< 5% |
B |
5 -10% |
C |
10-20% |
D |
20-30% |
E |
>30% |
Question 7.
Which, if any, of the following conditions are associated with an ↑
risk of Ls?
Option List
A |
acromegaly
+ Addison’s disease + coeliac disease + IBD + IDDM |
B |
acromegaly
+ disease + anosmia + coeliac disease + IBD |
C |
acromegaly
+ IBD + IDDM |
D |
acromegaly
+ IBD |
E |
Addison’s
disease + anosmia + coeliac disease + IBD + IDDM |
F |
acromegaly
+ Addison’s disease + anosmia + coeliac disease + IBD + IDDM |
G |
none of the above |
Question 8.
Which 2 cancers are most likely in women with Lynch syndrome?
Option List
A |
breast +
bowel |
B |
breast + pancreas |
C |
breast + endometrium |
D |
bowel + cervix |
E |
bowel + endometrium |
F |
bowel + ovary |
G |
bowel + pancreas |
H |
endometrium + ovary |
Question 9.
What does NICE recommend about screening for Lynch syndrome for the
population
with no
personal history of colorectal cancer?
Option List
A |
offer screening to those aged < 50 years with ≥ 1 affected 1st.O
relative |
B |
offer screening to those aged < 60 years with ≥ 1
affected 1st.O relative |
C |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 50 years at diagnosis |
D |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 60 years at diagnosis |
E |
none of the above |
Question 10.
What does NICE recommend in relation to screening for Lynch syndrome in
those with
a new
diagnosis of colorectal cancer?
Option List
A |
offer
screening to everyone, regardless of age and family history |
B |
offer screening to those aged < 50 years at diagnosis |
C |
offer screening to those aged < 60 years at
diagnosis |
D |
offer screening to those aged < 50 years at
diagnosis with + ≥ 1 affected 1st.O relative |
E |
offer screening to those aged < 60 years at
diagnosis with + ≥ 1 affected 1st.O relative |
Question 11.
What does NICE recommend about screening for Lynch syndrome for the
population
with no
personal history of thyroid cancer?
Option List
A |
offer screening to those aged < 50 years with ≥ 1 affected 1st.O
relative |
B |
offer screening to those aged < 60 years with ≥ 1
affected 1st.O relative |
C |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 50 years at diagnosis |
D |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 60 years at diagnosis |
E |
none of the above |
Question 12.
What does NICE recommend in relation to screening for Lynch syndrome in
those
with a new
diagnosis of thyroid cancer?
Option List
A |
offer
screening to everyone, regardless of age and family history |
B |
offer screening to those aged < 50 years at diagnosis |
C |
offer screening to those aged < 60 years at
diagnosis |
D |
offer screening to those aged < 50 years at
diagnosis with + ≥ 1 affected 1st.O relative |
E |
none of the above |
Question 13.
What does NICE recommend about screening for Lynch syndrome for the
population
with no personal history of endometrial
cancer?
Option List
A |
offer screening to those aged < 50 years with ≥ 1 affected 1st.O
relative |
B |
offer screening to those aged < 60 years with ≥ 1
affected 1st.O relative |
C |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 50 years at diagnosis |
D |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 60 years at diagnosis |
E |
none of the above |
Question 14.
What does NICE recommend in relation to screening for Lynch syndrome in
those with
a new diagnosis
of endometrial cancer?
Option List
A |
offer screening to those aged < 50 years with ≥ 1 affected 1st.O
relative |
B |
offer screening to those aged < 60 years with ≥ 1
affected 1st.O relative |
C |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 50 years at diagnosis |
D |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 60 years at diagnosis |
E |
none of the above |
Question 15.
What does NICE recommend about screening for Lynch syndrome for the
population
with no
personal history of colorectal cancer?
Option List
A |
offer screening to those aged < 50 years with ≥ 1 affected 1st.O
relative |
B |
offer screening to those aged < 60 years with ≥ 1
affected 1st.O relative |
C |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 50 years at diagnosis |
D |
offer screening to those with ≥ 1 affected 1st.O
relative aged < 60 years at diagnosis |
E |
none of the above |
Question 16.
What does NICE recommend in relation to screening for Lynch syndrome in
those with
a new
diagnosis of colorectal cancer?
Option List
A |
offer
screening to everyone, regardless of age and family history |
B |
offer screening to those aged < 50 years at
diagnosis |
C |
offer screening to those aged < 60 years at
diagnosis |
D |
offer screening to those aged < 50 years at
diagnosis with + ≥ 1 affected 1st.O relative |
E |
offer screening to those aged < 60 years at
diagnosis with + ≥ 1 affected 1st.O relative |
Question 17.
What relationship, if any, exists between Ls and acromegaly?
Option List
A |
the risk
of Ls is ↓
in those with acromegaly compared with the general population |
B |
the risk
of Ls is ↑
in those with acromegaly compared with the general population |
C |
the risk
of Ls is unchanged in those with acromegaly compared with the general
population |
D |
the risk
of Ls in unknown in those with acromegaly |
E |
|
Question 18.
What is the effect of aspirin consumption on the risk of EC and CRC?
Option List
A |
aspirin
reduces the risk of EC and CRC |
B |
aspirin
reduces the risk of EC but not CRC |
C |
aspirin
reduces the risk of CRC but not EC |
D |
aspirin
does not reduce the risk of EC or CRC |
E |
aspirin reduces the risk of EC and CRC, but the risks
outweigh the benefits |
Question 19.
A healthy woman of 35 years is diagnosed with Ls? What are the key
elements of the
National Screening
Programme for people with Ls?
There is
no option list – just write down everything you know.
Question
20. Which, if any, of the following were
recommendations made by Monahan et al, the 30
experts who wrote to the BMJ in 2017.
Option List
A |
creation of a national register of
people with Ls |
B |
creation of a
post of Consultant in Ls for each NHS Trust |
C |
creation of a
post of Clinical Champion for Ls in each NHS Region. |
D |
creation of a
post of Clinical Champion for Ls in the DOH. |
E |
none of the
above |
With regard to Lynch
syndrome,
1. loss of mismatch repair protein expression
on immunohistochemistry of cancer is diagnostic.
True/False
2. most carriers of the mutation associated
with the syndrome know they have the condition.
True/False
3. the first cancers associated with the
syndrome are predominantly endometrial or ovarian cancers. True/False
4. when cancers occur, they have in them an unusually
high immune infiltrate. True/False
With regard to testing for Lynch syndrome,
5. consent must be sought before definitive germline
testing for Lynch syndrome by a trained professional. True/False
6. immunohistochemical staining of tumours for
the mismatch repair proteins or microsatellite instability analysis are recognised
ways of screening cancers for characteristics suggestive of the syndrome. True/False
7. the National Institute for Health and Care Excellence
endorses universal screening of colorectal cancer patients for Lynch syndrome. True/False
8. most gynaecological cancers found to have aberrant
mismatch repair immunohistochemical staining will be in those with the
syndrome. True/False
9. the addition of MLH1 promotor hypermethylation
testing in a Lynch syndrome diagnostic pathway improves specificity. True/False
Regarding gynaecological surveillance in women with Lynch
syndrome,
10. there is strong evidence to recommend its use.
True/False
11. this should be offered to women around 25 years
of age. True/False
12. counselling should include education on red flag
symptoms of cancer and risk-reducing surgery.
True/False
With regard to risk-reducing strategies for women with Lynch
syndrome,
13. hysterectomy is strongly recommended for all those
with the syndrome. True/False
14. the timing of risk-reducing surgery depends on
the syndrome gene. True/False
15. where possible, a laparoscopic approach is
recommended. True/False
16. aspirin is not recommended as a means of reducing
their overall cancer risk. True/False
Regarding Lynch syndrome-associated gynaecological
cancers,
17. endometrial types that arise as a result of
the syndrome have a poorer prognosis than sporadic types. True/False
18. checkpoint inhibition of the PD-1/PD-L1 pathway
has been shown to be very effective in mismatch repair-deficient cancers. True/False
19. vaccination against these cancers is currently
the focus of research. True/False
20. the Manchester International Consensus guideline
is a useful reference for gynaecologists managing women with these cancers. True/False
59. Toxoplasmosis.
Abbreviations.
cTg: congenital toxoplasmosis.
TgIgG: Toxoplasmosis
immunoglobulin G.
TgIgM: Toxoplasmosis immunoglobulin M.
Question
1.
Which, if any, of
the following are true in relation to the organism causing
toxoplasmosis.
Option list.
A |
it is Toxoplasma giardia |
B |
it is Toxoplasma gondi |
C |
it is Toxoplasma gondii |
D |
it is Toxoplasma gondola |
E |
it is Toxoplasma gung-ho |
F |
none of the above |
Question
2.
Approximately what
proportion of the UK pregnant population shows evidence of
previous Tg infection?
Option list.
A |
< 10% |
B |
10% |
C |
20% |
D |
30% |
E |
40% |
F |
50% |
G |
> 50% |
Question
3.
When is maternal
infection believed to be of greatest risk to the fetus?
Option list.
A |
peri-conceptually |
B |
1st. trimester |
C |
2nd. trimester |
D |
3rd. trimester |
E |
during vaginal birth |
F |
in the puerperium |
G |
in the puerperium if breastfeeding |
H |
none of the above |
Question
4.
Which, if any, of the following are true with regard to when
tgIgG is detectable after
1ry maternal infection?
Option list.
A |
2 weeks |
B |
4 weeks |
C |
2 months |
D |
3 months |
E |
6 months |
F |
none of the above |
Question
5.
Which, if any, of the following are true with regard to when TgIgM
is detectable after
1ry maternal infection?
Option list.
A |
2 weeks |
B |
4 weeks |
C |
2 months |
D |
3 months |
E |
6 months |
F |
none of the above |
Question
6.
Which, if any, of the following are true with regard to
avidity testing for Tg?
Option list.
A |
avidity testing is of little use |
B |
avidity testing requires expert advice |
C |
avidity < 30% indicates infection in the previous 3
months |
D |
avidity < 30% indicates infection in the previous 6
months |
E |
avidity < 30% indicates infection in the previous 9 months |
F |
avidity > 40% indicates infection more than 3 months
previously |
G |
avidity > 40% indicates infection more than 6 months
previously |
H |
avidity > 40% indicates infection more than 9 months
previously |
I |
none of the above |
Question
7.
Which, if any, of the following are true with regard to confirmation
of fetal infection?
Option list.
A |
avidity testing is of little use |
B |
avidity testing requires expert advice |
C |
avidity < 30% indicates infection in the previous 3
months |
D |
avidity < 30% indicates infection in the previous 6
months |
E |
avidity < 30% indicates infection in the previous 9 months |
F |
avidity > 40% indicates infection more than 3 months
previously |
G |
avidity > 40% indicates infection more than 6 months
previously |
H |
avidity > 40% indicates infection more than 9 months
previously |
I |
none of the above |
Question
8.
Which, if any, of
the following are true in relation to the NSC’s decision on routine
toxoplasmosis screening in
pregnancy in 2016?
Option list.
A |
screening should be introduced as soon as practicable |
B |
testing would produce a falsely-high prevalence of Tg
in pregnancy |
C |
the prevalence of Tg is too low for screening to be
cost-effective |
D |
the prevalence of Tg is high enough for screening to be cost-effective |
E |
the prevalence of Tg is unknown |
F |
there is no treatment in pregnancy of proven benefit to
mother or baby |
G |
they would leave the decision until after lunch, but
drank too much wine and did not return |
H |
maybe some of the above, please tick the boxes for me |
I |
none of the above |
Question 9.
Which, if any, of
the following are complications of intrauterine Tg infection for the fetus and newborn.
Option list.
A |
miscarriage |
B |
IUGR |
C |
stillbirth |
D |
chorioretinitis |
E |
hepato-splenomegaly |
F |
holoprosencephaly |
G |
hydrocephalus |
H |
intracranial calcification |
I |
microcephaly |
J |
neural tube defect |
Question
10. Approximately how common in vertical transmission of Tg in
the 1st. trimester?
Option list.
A |
< 10% |
B |
10-20% |
C |
25% |
D |
50% |
E |
> 50% |
Question
11. Approximately how common in vertical transmission of Tg in
the 2nd. trimester? Use
the option list for question 4.
Option list.
A |
< 10% |
B |
10-20% |
C |
25% |
D |
50% |
E |
> 50% |
Question 12.
Approximately how
common in vertical transmission of Tg in the 3rd. trimester? Use the
option list for question 4.
Option list.
A |
< 10% |
B |
10-20% |
C |
25% |
D |
50% |
E |
> 50% |
Question 13.
Which of the
following are true in relation to reducing the risk of vertical transmission of
Tg?
Option list.
A |
the SYROCOT trial showed strong evidence of the
efficacy of spiramycin |
B |
a Cochrane trial has suggested that pyrimethamine +
sulfadiazine give better results than spiromycin |
C |
there is evidence that metronidazole is the most
effective drug |
D |
there is a lack of clear evidence about effective
therapies |
E |
spiromycin crosses the placenta, so is effective in
reducing MTBT and treating the infected fetus |
E |
this is too esoteric for my poor pummelled brain |
Question 14.
Which, if any, of
the following are features of the classical triad associated with congenital
Tg?
Option list.
A |
chorioretinitis |
B |
deafness |
C |
hepatosplenomegaly |
D |
hydrocephalus |
E |
intracranial calcifications |
F |
low birthweight |
G |
jaundice |
H |
leukopenia |
Question
15. Which of the following are used in the treatment of cTg?
Option list.
A |
metronidazole |
B |
pyrimethamine |
C |
steroids |
D |
sulfadiazine |
E |
none of the above. |
60. Quinolone & fluoroquinolone antibacterial drugs
Abbreviations.
FQ: fluoroquinolone.
MHRA: UK’s Medicines and Healthcare products Regulatory
Agency.
SLE: systemic lupus erythematosus.
QUI: quinolone.
Question 1. Which, if any, of the following drugs
are QUIs or FQs?
Drugs
A |
cimetidine
|
B |
ciprofloxacin |
C |
nalidixic acid |
D |
neomycin |
E |
nitrofurantoin |
Option List
1 |
A + B |
2 |
A + B + C |
3 |
B + C |
4 |
B + C + D + E |
5 |
A + B + C + D + E |
Question 2. Which, if any, of the following
statements are true in relation to QUIs & FQs? This is
not a true
SBA as there may be more than one answer.
Statements
A |
nalidixic
acid is an older quinolone and is mainly excreted in the urine |
B |
ciprofloxacin is effective against most Gram +ve and
–ve bacteria and 1st- line treatment for pneumococcal pneumonia. |
C |
ciprofloxacin is contraindicated in pregnancy due to
the ↑ risk of neonatal haemolysis |
D |
many staphylococci are resistant to quinolones |
E |
quinolones are particularly useful in the treatment of
MRSA |
Question 3. Which was the first QUI antibiotic?
Option List
A |
acetylsalicylic
acid |
B |
nalidixic
acid |
C |
oxalic
acid |
D |
pipemidic
acid |
E |
none of
the above |
Question 4. How do QUI and FQ antibiotics work?
There is only one correct answer.
Option List
A |
impair
bacterial DNA coiling |
B |
impair
bacterial DNA binding |
C |
impair
bacterial RNA action |
D |
impair
bacterial mitochondrial action |
E |
none of
the above. |
Question 5. Which, if any, of the following QUIs
& FQs is not available for prescription in the UK.
There is
only one correct answer.
Option List
A |
ciprofloxacin |
B |
levofloxacin |
C |
nalidixic
acid |
D |
moxifloxacin |
E |
ofloxacin |
Question 6. Which, if any, of the following
statements are true in relation to the quinolones and
fluoroquinolones
and pregnancy? This is not a true SBA as there may be more than one answer.
Option list.
A |
FQs are
newer than QUIs with better systemic spread and efficacy |
B |
QUIs concentrate in urine but have a special affinity
for cartilage |
C |
consumption of a FQ in the 1st. trimester is
grounds for TOP |
D |
if an FQ is used, norfloxacin and ciprofloxacin should
be considered 1st. |
E |
FQs are linked to a risk of discolouration of the teeth
of offspring |
Question 7. Which of the following is true about
the warning issued by the FDA in 2008 in relation
to QUIs
& FQs?
Option List
A |
they may
cause congenital cartilage defects |
B |
they may
cause congenital deafness |
C |
they may
cause tendonitis and tendon rupture |
D |
they may
cause prolongation of the Q-T interval |
E |
none of
the above |
Question 8. Which of the following is true about
the warning issued by the FDA in 2011 in relation
to QUIs
& FQs?
Option List
A |
they may
cause exacerbation of eczema |
B |
they may
cause exacerbation of hypertension |
C |
they may
cause exacerbation of multiple sclerosis |
D |
they may
cause exacerbation of myasthenia gravis |
E |
they may
cause exacerbation of SLE |
Question 9. Which of the following is true about the
warning emphasised by the FDA in 2013 in
relation
to QUIs & FQs?
Option List
A |
they may
cause aortic dissection |
B |
they may
cause mitral stenosis |
C |
they may
cause pancreatitis |
D |
they may
cause peripheral neuropathy |
E |
they may
cause flare of SLE |
Question 10. FDA issued a warning in July 2016.
Which, if any, of the following were included? This
is not a
true SBA as there may be more than one answer.
Option List
A |
the
risks generally outweigh the benefits |
B |
QUIs
& FQs should not be used for acute
sinusitis, |
C |
QUIs
& FQs should not be used for exacerbation
of chronic bronchitis |
D |
QUIs
& FQs should not be used for uncomplicated
UTI |
E |
QUIs
& FQs may be useful for anthrax and plague |
Question 11. FDA issued a warning in July 2018
about the use of FQs in pregnancy. Which, if any, of
the
following were included in the reasons for its publication?
Option List
A |
to
strengthen previous warnings about hyperglycaemia and mental health risks |
B |
to
strengthen previous warnings about hypoglycaemia and mental health risks |
C |
to
strengthen previous warnings about the risk of ASD in the offspring |
D |
to
strengthen previous warnings about the risk of acute pancreatitis |
E |
to
strengthen previous warnings about the risk of PET |
Question 12. The FDA issued a warning in December 2018
about the use of FQs in pregnancy.
Which, if
any, of the following was included? This is an SBA with only one correct
answer.
Option List
A |
↑ risk of atrial
fibrillation |
B |
↑ risk of aortic
aneurysm and rupture |
C |
↑ risk of
mitral stenosis |
D |
↑ risk of
pulmonary hypertension |
E |
↑ risk of
ulcerative colitis |
61. Listeriosis
and pregnancy.
Lm: Listeria monocytogenes.
TOC: test of cure.
Scenario
1.
Which organism is
responsible for human listeriosis?
A |
Listeria diogenys |
B |
Listeria frigidaire |
C |
Listeria hominis |
D |
Listeria monocytogenes |
E |
Listeria xenophylus |
Scenario
2.
Which, if any, of
the following statements are true about Lm?
Option list.
A |
it is a small, Gram -ve rod |
B |
it is a Gram +ve coccus |
C |
it is flagellated |
D |
it has no cell wall |
E |
it is an obligate aerobe |
F |
it functions within host cells |
G |
it can easily be mistaken for commensal organisms |
H |
none of the above |
Scenario
3.
Which of the
following are associated with an increased risk of contracting LM?
A |
age > 60 years |
B |
age < 1 year |
C |
blond hair |
D |
pregnancy |
E |
strabismus |
Scenario 4.
Which of the following
are true of the susceptibility of pregnant women to Lm?
Option list.
A |
they are not more susceptible |
B |
they are more susceptible x 2 |
C |
they are more susceptible x 5 |
D |
they are more susceptible x 10 |
E |
they are more susceptible x 20 |
F |
they are > 20 times more susceptible |
G |
none of the above. |
Scenario
5.
When does Lm most
often occur?
Option list.
A |
1st. trimester |
B |
2nd. trimester |
C |
3rd trimester |
D |
1st. + 2nd. trimesters |
E |
2nd. + 3rd trimesters |
F |
all trimesters equally |
G |
puerperium |
H |
none of the above |
Scenario
6.
What is the incubation
period for Lm?.
Option list.
A |
7±3 days |
B |
7±5 days |
C |
10±3 days |
D |
10±5 days |
E |
14±3 days |
F |
14±5 days |
G |
none of the above. |
Scenario
7.
What is the
significance of Granulomatosis Infantisepticum ?
Option list.
A |
it is a
fabrication by the author and of no significance |
B |
it is pathognomonic
of Lm infection |
C |
it is the cause
of vertical transmission of Lm |
D |
I refuse to
answer Latin questions as they make me think of Boris Johnson |
E |
none of the above |
Scenario
8.
Which of the following
are accurate about cervico-vaginal infection? This is not a true
EMQ as there may be >1 correct answer.
Option list.
A |
Lm is as often found in the cervix as in the bowel. |
B |
Lm is as often found in the vagina as in the bowel. |
C |
Lm is less often found in the cervix than in the bowel. |
D |
Lm is less often found
in the vagina than in the bowel. |
E |
Lm is more often found in the cervix than in the bowel. |
F |
Lm is more often found in the cervix than in the bowel. |
G |
no one knows and no one cares |
Scenario
9.
A GP phones about
a primigravida at 28 weeks. She has possibly ingested food
contaminated by Lm. She is asymptomatic and afebrile. What
advice will you give?
Option list.
A |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 2 weeks |
B |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 4 weeks |
C |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 6 weeks |
D |
reassure and advise her about avoiding exposure and to reattend
if she develops signs or symptoms within 8 weeks |
E |
prescribe appropriate antibiotic(s) for 7 days with
follow-up for TOC |
F |
prescribe appropriate antibiotic(s) for 7 days with
follow-up for TOC |
G |
prescribe appropriate antibiotic(s) for 7 days with
follow-up for TOC |
H |
admit to hospital for investigation and intensive
treatment if Lm infection found |
I |
none of the above |
Scenario
10. A GP phones about a primigravida at 28 weeks. She has possibly
ingested food
contaminated by Lm. She has mild symptoms but is afebrile.
What advice will you give?
Option list.
A |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 2 weeks |
B |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 4 weeks |
C |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 6 weeks |
D |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 8 weeks |
E |
prescribe appropriate antibiotic(s) for 7 days with
follow-up for TOC |
F |
prescribe appropriate antibiotic(s) for 7 days with
follow-up for TOC |
G |
prescribe appropriate antibiotic(s) for 7 days with
follow-up for TOC |
H |
admit to hospital for investigation and intensive
treatment if Lm infection found |
I |
none of the above |
Scenario
11. A GP phones about a primigravida at 28 weeks. She has possibly
ingested food
contaminated by Lm. She is symptomatic and her temperature
is 38.2oC. What advice will you give?
Option list.
A |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 2 weeks |
B |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 4 weeks |
C |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 6 weeks |
D |
reassure and advise her about avoiding exposure and to
reattend if she develops signs or symptoms within 8 weeks |
E |
prescribe appropriate antibiotic(s) for 7 days with
follow-up for TOC |
F |
prescribe appropriate antibiotic(s) for 7 days with
follow-up for TOC |
G |
prescribe appropriate antibiotic(s) for 7 days with
follow-up for TOC |
H |
admit to hospital for investigation and intensive
treatment if Lm infection found |
I |
none of the above |
Scenario
12. Which, if any, of the following would be appropriate for
consideration as 1st. line
treatment of Lm in pregnancy? This is not a true EMQ as
there may be more than 1 correct answer.
Option list.
A |
ampicillin |
B |
ampicillin + gentamycin |
C |
ampicillin + streptomycin |
D |
amoxicillin + clavulanic acid |
E |
clarithromycin |
F |
erythromycin |
G |
erythromycin + metronidazole |
H |
trimethoprim |
I |
none of the above |
Scenario
13. Is listeriosis a notifiable infection in the UK? Yes/No.
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