Monday, 25 July 2022

Tutorial 25th. July 2022

 

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27

Role-play. Break bad news. Non-viable early pregnancy.

28

EMQ. Kallmann’s syndrome

29

SBA. Tamoxifen

30

EMQ. Listeriosis and pregnancy

31

SBA.   Lynch syndrome

32

EMQ. Flu and pregnancy

 

27.   Role-play. Break bad news. Non-viable early pregnancy.

Candidate’s instructions.

You are the SpR in the ante-natal clinic. The consultant who was in clinic has been asked to assist her consultant colleague in the labour ward theatre. She is unlikely to return for some time as the case is one of massive PPH and hysterectomy may be necessary. 

One of the midwives asks you to see Jane Brown, who has just had a scan in the early pregnancy unit.  She is primigravid and the gestation is 8 weeks. She has had some bleeding.   

An ultrasound scan = IUP.  CRL = 12 mm.  No fetal heart activity.  No adnexal masses.

 

28.   Kallmann’s syndrome

Abbreviations.

Ks:         Kallmann’s syndrome

Scenario 1.              

Which of the following might be included in descriptions of Kallmann’s syndrome?

Option list.

A

hypogonadotrophic hypogonadism

B

hypogonadotrophic hypogonadism + anosmia

C

hypogonadotrophic hypogonadism + anosmia + colour-blindness.

D

hypogonadotrophic hypogonadism due to uterine agenesis

Scenario 2.              

Lead in.

Which, if any, of the following are features of the Kallmann phenotype?

A

absent or minimal breast development

B

aortic stenosis

C

blue eyes

D

blue hair

E

hot flushes

F

short stature

G

tall stature

H

vaginal agenesis

I

none of the above

Scenario 3.              

How common is Kallmann’s syndrome and what is the female: male ratio?

A

1 in 1,000 and F:M ratio 1:1

B

1 in 5,000 and F:M ratio 1:1

C

1 in 10,000 and F:M ratio 1:4

D

1 in 50,000 and F:M ratio 1:4

E

1 in 100,000 and F:M ratio 1:8

F

1 in 250,000 and F:M ration 1:10

Scenario 4.              

What is the most common mode of inheritance of Ks?

Option list.

A

hypogonadotrophic hypogonadism

B

hypogonadotrophic hypogonadism + anosmia

C

hypogonadotrophic hypogonadism due to uterine agenesis

D

autosomal dominant

E

autosomal recessive

F

X-linked recessive

G

new mutation of the ANOS1 gene

H

the most common mode of inheritance is not known

Scenario 5.              

How is Kallmann’s syndrome diagnosed?

A

abdominal and pelvic ultrasound scan

B

cell-free fetal DNA

C

chromosome analysis

D

CT scan of hypothalamus / pituitary

E

MR scan of hypothalamus / pituitary

F

none of the above.

Scenario 6.              

How is Kallmann’s syndrome treated initially?

Which of the following statements are true?

Option list.

A

GnRH analogue depot

B

pulsatile GnRH therapy

C

combined oral contraceptive

D

counselling & education re gender re-assignment

E

depot progestogen

F

none of the above

Scenario 7.              

A woman was diagnosed with Kallmann’s syndrome at 16 and had successful initial treatment. She is now 25, married and wishes to have a pregnancy. She has had pre-pregnancy assessment and counselling. Which of the following should be considered?

A

GnRH analogue depot

B

induction of ovulation with clomiphene

C

gonadotrophin therapy

D

pulsatile GnRH therapy

E

none of the above

 

29.   Tamoxifen

Abbreviations.

HER2:            Human epidermal growth factor receptor 2.

SERM:           selective oestrogen receptor modulator

Question 1.    What kind of drug is Taxoxifen?

Option List

A

aromatase inhibitor

B

GnRH analogue

C

selective anti-oestrogen

D

selective oestrogen-receptor blocker

E

selective oestrogen receptor modulator.

Question 2.    Which of the following are current indications for using tamoxifen?

Option List

A

reducing risk of development of breast cancer in women +ve for BRCA1 & 2

B

treatment of oestrogen receptor –ve breast cancer

C

treatment of oestrogen receptor +ve breast cancer

D

treatment of HER2 –ve breast cancer

E

treatment of HER2 +ve breast cancer

Question 3.    How do aromatase inhibitors work?

Option List

A

negate the olfactory-ovarian feedback loop’s effects

B

reduce DNA replication and cell division

C

reduce FSH production and oestrogen levels in premenopausal women

D

reduce production of oestrogen from androgen

E

none of the above

Question 4.    How do SERMS work?

Option List

A

competitive binding to oestrogen-receptors

B

competitive binding to oestrogen-receptors in granulosa cells

C

competitive binding to oestrogen-receptors in the anterior pituitary

D

increased oestrogen receptor apoptosis

E

none of the above

Question 5.    What have been the main uses of tamoxifen in gynaecology?

Option List

A

peri and postmenopausal oestrogen replacement therapy

B

contraception, though no longer used

C

ovulation induction as an alternative to clomifene

D

osteoporosis prevention in premature ovarian insufficiency

E

none of the above

Question 6.    Which, if any,  of the following are recognised side-effects of tamoxifen?

Option List

A

risk of cataract and retinopathy

B

risk of endometrial pathology, including cancer

C

risk of thrombocytopenia

D

risk of thrombosis and VTE by a factor of 2-3

E

menopausal symptoms: hot flushes & sweats

Question 7.    Which, if any, of the following statements are true in relation to the risk of uterine

cancer in women using Tamoxifen?

Option List

A

the overall risk of endometrial cancer  is increased by a factor of 2-3

B

the overall risk of endometrial cancer is increased by a factor of 5-10

C

the risk of endometrial cancer  is not increased in postmenopausal women

D

the risk of endometrial cancer is increased by 50% in premenopausal women

E

the risk is endometrial cancer is increased, but the risk of sarcoma is not

Question 8.    Which, if any, of the following statements are true in relation to the risk of thrombosis

and VTE in women using Tamoxifen?

Option List

A

the risk is increased by a factor of 1.5-2

B

the risk is increased by a factor of 2-3

C

the risk is increased by a factor of 5-10

D

the risk increases with age

E

the risk increases if chemotherapy is given at the same time

Question 9.    Which, if any, of the following statements are true?

Option List

A

tamoxifen is metabolised by cytochrome P450 34A

B

tamoxifen is metabolised by cytochrome P450 34B

C

inducers of the relevant P450 enzyme reduce tamoxifen levels

D

inducers of the relevant P450 enzyme reduce the efficacy of tamoxifen

E

fluoxetine is a potent inducer of the relevant P450 enzyme

Question 10.  Which, if any, of the following statements are true?

Option List

A

endoxifen is a main active metabolite of tamoxifen

B

cytochrome P450 2D6 reduces endoxifen levels

C

cytochrome P450 2D6 inducers can reduce tamoxifen’s efficacy

D

fluoxetine is a potent inducer of cytochrome P450 2DS

E

paroxetine is a potent inducer of cytochrome P450 2DS

 

30.   Listeriosis

Abbreviations.

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.

 

31.   SBA.   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

 

32.   EMQ. Flu and pregnancy

Abbreviations.

GB19:              The DOH’s book: “Immunisation against infectious disease”, commonly known as the “Green Book”. Chapter_19_influenza_October_2020.

DOH:                Department of Health

JCVI:                 Joint Committee on Vaccination and Immunisation

MBRRACE:      MBRRACE-UK: Mothers and Babies: Reducing Risk through Audits and Confidential Enquiries across the UK.

PHE:                 Public Health England.

WHO:              World Health Organisation

Question 1. What did MBRRACE say about flu & pregnancy in its first report in 2014?

Option List

A

1 in 11 women died from flu

B

1 in 11 women died from flu and flu vaccination could have prevented ½ of the deaths

C

1 in 21 women died from flu

D

1 in 21 women died from flu and flu vaccination could have prevented ½ of the deaths

E

1 in 51 women died from flu

F

1 in 51 women died from flu and flu vaccination could have prevented ½ of the deaths

Question 2. How many types of flu virus are recognised?

Option List

A

3

B

5

C

10

D

15

E

>100

Question 3. Why can’t we have a universal flu vaccine?

List of statements.

A

The main surface antigens are haemagglutinin and neuraminidase

B

The main surface antigens are haemolysin and neuroxidase

C

The main surface antigens change frequently rendering existing vaccines impotent

D

The main core antigens change frequently, rendering existing vaccines impotent

E

The big drug companies avoid making a universal vaccine for financial reasons.

Question 4. When is flu’ most often a problem in the UK?

Option List

A

Spring

B

Summer

C

Autumn

D

Winter

E

None of the above.

Question 5. How is flu spread?

Option List

A

via aerosol or droplets from respiratory tract of an infected person

B

via aerosol or droplets from respiratory tract or direct contact with respiratory secretions  of an infected person

C

from getting drenched in cold winter showers

D

from thinking lascivious thoughts

E

from toilet seats

Question 6. What is the incubation period for flu?

Option List

A

1 – 3 days

B

1 – 7 days

C

5 – 10 days

D

up to 2 weeks

E

up to 3 weeks

Question 7. Who decides which viruses will be used in the vaccine for seasonal flu?

Option List

A

DOH

B

JCVI

C

the Prime Minister

D

the vaccine manufacturers

E

WHO

Question 8. How long has flu vaccination been recommended in the UK?

Option List

A

since the 1950s

B

since the 1960s

C

since the 1970s

D

since the 1980s

E

since the 1990s

Question 9. What is the recommendation about when the vaccine should be given?

Option List

A

May - July

B

June - August

C

July - September

D

August - October

E

September - November

Question 10. What advice is given about vaccination in pregnancy?

Option List

A

flu vaccine is potentially teratogenic and should be avoided before 16 weeks

B

the vaccine contains an attenuated virus with no evidence of risk in pregnancy

C

the vaccine recommended for pregnancy has no live viral material and all pregnant women are encouraged to have the seasonal vaccine

D

flu vaccine contains an attenuated virus with minimal risk, but the anti-viral drug Tamiflu is given with the vaccine to eliminate any risk of harm

Question 11. What is the H1N1 virus?

Option List

A

The avian virus which causes outbreaks of “bird flu”

B

The virus associated with “swine” flu, which caused a pandemic in 2009

C

The virus associate with MERS, currently causing deaths particularly in Saudi Arabia

D

The virus associated with simian flu

E

The virus associated with the pandemic of 1915.

Question 12. What advice should be given to pregnant women about protection against the H1N1 virus?

Option List

A

to have vaccination against H1N1 in addition to the seasonal vaccine

B

to have vaccination against H1N1 in preference to the seasonal vaccine

C

to await evidence of epidemic H1N1 flu and then have vaccination against H1N1

D

to have the seasonal vaccine as it gives good protection against H1N1

E

not to have any flu vaccination, but to take antiviral drugs if symptoms of flu occur

Question 13. Which of the following conditions have been linked to flu in pregnancy?

Conditions.

A

­ risk of flu complications for the mother

B

­ risk of low birthweight

C

­ risk of maternal death

D

­ risk of perinatal death

E

­ risk of  prematurity

Question 14. What is the estimated uptake of flu vaccination by pregnant women in the UK?

Pick the best option from the following list.

Option List

A

20-30%

B

30-40%

C

40-50%

D

50-60%

E

> 60%

Question 15. How many maternal deaths from flu were reported by MBRRACE for the years 2012 - 2013?

Pick the best option from the following list.

Option List

A

0

B

5

C

10

D

15

E

20

Question 16. With regard to the probable explanation for the numbers of maternal deaths from ‘flu in 2012 and 2013, which, if any, of the following statements is true?

Option List

A

the numbers reflected increased prevalence of ‘flu

B

the numbers reflected reduced prevalence of ‘flu

C

the numbers reflected improved uptake of ‘flu vaccine in pregnancy

D

the numbers reflected the introduction of Tamiflu for pregnant women with ‘flu

E

none of the above

 

 

 

 


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