Thursday, 19 November 2020

Tutorial 19th. November 2020

19 November 2020

 

11

EMQ. Hepatitis B.

12

EMQ. Peutz-Jeghers syndrome.

13

EMQ Tranexamic acid.

14

EMQ. G6PDD & G6PD

15

EMQ. Caldicott guardian

 

11. EMQ. Hepatitis B and pregnancy.

Abbreviations.

HAV:          hepatitis A virus

HBcAg:      hepatitis B core antigen

HBeAg:      hepatitis B e antigen           

HBsAg:      hepatitis B surface antigen

HBcAb:      antibody to hepatitis B core antigen

HBeAb:     antibody to hepatitis B e antigen

HBsAb:      antibody to hepatitis B surface antigen

HBIG:         hepatitis B immunoglobulin

HBV:          hepatitis B virus

HBcAg:      hepatitis B core antigen

HBeAg:      hepatitis B e antigen           

HBsAg:      hepatitis B surface antigen

HBcAb:      antibody to hepatitis B core antigen

HBeAb:     antibody to hepatitis B e antigen

HBsAb:      antibody to hepatitis B surface antigen

HBIG:         hepatitis B immunoglobulin

HCV:          hepatitis C virus

HEV:          hepatitis E virus

HSV:          herpes simplex virus

VT:             vertical transmission

Option list.

A.      

acyclovir 

B.      

divorce

C.      

HBcAg +ve

D.      

HBeAg +ve

E.       

HbsAg +ve

F.       

HBsAg +ve; HBsAb –ve;  HBcAb –ve; HBeAg +ve

G.      

HBsAg +ve; HBsAb –ve on two tests six months apart

H.      

HBsAg -ve; HBsAb -ve on two tests six months apart

I.        

HBsAg -ve; HBsAb +ve; HBcAb –ve

J.        

HBsAg -ve; HBsAb +ve; HBcAb +ve

K.      

HBsAg -ve; HBsAb +ve

L.       

HBsAg +ve; HBcAg +ve

M.    

HBV vaccine

N.      

HBIG

O.     

HBV vaccine + HBIG

P.      

immune as a result of infection

Q.     

immune as a result of vaccination

R.      

not immune

S.       

chronic carrier of HBV infection

T.       

10%

U.      

30%

V.      

50%

W.    

60%

X.      

70-90%

Y.       

soap and boiling water

Z.       

10% dilution of bleach in water

AA.  

10% dilution of formaldehyde in alcohol

BB.  

ultraviolet irradiation

CC.   

yes

DD. 

no

EE.   

HAV

FF.    

HBV

GG.                      

HCV

HH.                      

HEV

II.       

HSV

JJ.      

none of the above

Question 1.          

An asymptomatic primigravida books at 10 weeks. Her partner had an acute HBV infection 4 months ago. What results on routine blood testing would indicate that she has an acute HBV infection?

Question 2.          

An asymptomatic primigravida books at 10 weeks. Her partner had an acute HBV infection 4 months ago. What results on routine blood testing would indicate that she is immune to the HBV as a result of infection?

Question 3.          

An asymptomatic primigravida books at 10 weeks. Her partner had an acute HBV infection 4 months ago. What results on routine blood testing would indicate that she is immune to the HBV as a result of HBV vaccine?

Question 4.          

An asymptomatic primigravida books at 10 weeks. Her partner had an acute HBV infection 9 months ago. What results on routine blood testing would show that she is a chronic carrier of HBV infection?

Question 5.          

Testing shows that he is positive for HBsAg, positive for HBcAb but negative for IgM HBcAb. What does this mean in relation to his HBV status?

Question 6.          

Testing shows that he is negative for HBsAg, positive for HBcAb and positive for HBsAb.

What does this mean in relation to his HBV status?

Question 7.          

How common is chronic HBV carrier status in UK pregnant women?

Question 8.          

What is the risk of death from chronic HBV carrier status?

Question 9.          

A primigravid woman at 8 weeks gestation is found to be non-immune to HBV. She has recently married and her husband is a chronic carrier. What should be done to protect her from infection?

Question 10.      

A woman is a known carrier of HBV. What is the risk of vertical transmission in the first trimester?

Question 11.      

What is the risk of the neonate who has been infected by vertical transmission becoming a carrier without treatment?

Question 12.      

Should antiviral maternal therapy in the 3rd. trimester be considered for women with HBeAg or high viral load?

Question 13.      

How effective is hepatitis B prophylaxis for the neonate in preventing chronic carrier status as a result of vertical transmission?

Question 14.      

Can a woman who is a chronic HBV carrier breastfeed safely?

Question 15.      

Hepatitis B infection is the most dangerous of the viral hepatitis infections in pregnancy.

Question 16.      

A pregnant woman who is not immune to HBV has a partner who is a chronic carrier. Can HBV vaccine be administered safely in pregnancy?

Question 17.      

How long can HBV survive outside the body?

Option list.

A

< 1 hour

B

up to 6 hours

C

up to 12 hours

D

up to 24 hours

E

up to 2 days

F

up to 5 days

G

at least 7 days

 

 

 

 

 

 

 

 

Question 18.      

A pregnant woman who is not immune has a partner with acute hepatitis due to HBV. He cuts his hand and bleeds onto the kitchen table. How should she clean the surface to ensure that she gets rid of the virus?

Question 19.      

Is it true that the presence of HBeAg in maternal blood is a particular risk factor for vertical transmission? Not really a scenario, but never mind!

Question 20.      

What does 5 log10 copies /mL mean?

A

> 10 copies / mL

B

> 100 copies / mL

C

> 1,000 copies / mL

D

> 10,000 copies / mL

E

> 100,000 copies / mL

F

this has scared me witless and I am going straight home to complain to my Mum

Question 21.      

Which, if any, of the following statements are true about amniocentesis and CVS and the risk of vertical transmission if the mother is HbsAg+ve?

Option list.

A

they are contraindicated

B

they should be done with cover with HBIG

C

they should be done with cover with a drug that is  effective for HBV and safe in pregnancy.

D

none of the above

Question 22.      

Which, if any, of the following statements are true about treatment in the third trimester to reduce the risk of vertical transmission?

Option list.

A

women who are HbsAg+ve should be offered testing for HBV DNA levels in the 3rd. trimester

B

there is no effective treatment for HBV in the 3rd. trimester

C

the risks of treatment for HBV in the 3rd. trimester outweigh the benefits

D

drug treatment for HBV in the 3rd. trimester adds nothing beneficial  to the normal use of HBIG + HB vaccination of the neonate

E

none of the above.

Question 23.      

Which, if any, of the following drugs is recommended for use in the third trimester to reduce the risk of vertical transmission?

Option list.

A

acyclovir 

B

lamivudine

C

telbivudine

D

tenofovir

Question 24.      

Does elective Cs before labour and with the membranes intact reduce the vertical transmission rate?

Question 25.      

Which hepatitis virus normally produces a mild illness, but represents a major risk to pregnant women, with a mortality rate of up to 5%?

Question 26.      

A pregnant woman has a history of viral hepatitis and informs the midwife at booking that she is a carrier and that she has a significant risk of cirrhosis and has been advised not to drink alcohol. Which is the most likely hepatitis virus?

Question 27.      

Which hepatitis virus is an absolute contraindication to breastfeeding after appropriate treatment of the infected mother and prophylaxis for the baby?

Question 28.      

Which hepatitis virus is linked to an increased risk of obstetric cholestasis?

 

12. EMQ. Peutz-Jeghers syndrome.

Abbreviations.

PJS:      Peutz-Jeghers syndrome.

Scenario 1.           

Which, if any, of the following are characteristics of PJS?

Option list.

A.      

buccal pigmentation

B.      

gastro-intestinal hamartomas

C.      

perianal pigmentation

D.      

increased risk of breast cancer

E.       

increased risk of cervical adenoma malignum

F.       

increased risk of colo-rectal cancer

G.      

increased risk of endometrial cancer

H.      

increased risk of ovarian cancer

I.        

increased risk of pancreatic cancer

J.        

increased risk of prostate cancer

K.      

increased risk of stomach cancer

Scenario 2.           

What is the approximate prevalence of PJS?

Option list.

A.      

< 1 in 1,000

B.      

1 in 1,000 to 1 in 10,000

C.      

1 in 10,000 to 1 in 100,000

D.      

1 in 25,000 to 1 in 100,000

E.       

1 in 25,000 to 1 in 200,000

F.       

1 in 25,000 to 1 in 300,000

G.      

1 in 300,000 to 1 in 500,000

H.      

< 1 in 500,000

Scenario 3.           

What is the mode of inheritance in PJS?

Option list.

A

autosomal dominant

B

autosomal recessive

C

X-linked dominant

D

X-linked recessive

E

Y-linked dominant

F

Y-linked recessive

G

triplet repeat

Scenario 4.           

Which, if any, of the following statements are true of PJS?

Option list.

A

PJS only occurs in families with other affected members

B

PJS mainly occurs in families with other affected members

C

PJS may arise de-novo in families with no other affected members

D

PJS may arise de-novo in families with other affected members

E

PJS does not arise de-novo in families with no other affected members

Scenario 5.           

What is the approximate lifetime risk of developing cancer in PJS?

Option list.

A.      

10%

B.      

20%

C.      

30%

D.      

40%

E.       

50%

F.       

60%

G.      

70%

H.      

80%

I.        

90%

J.        

>90%

Scenario 6.           

What is the relevance of STK11 to PJS?

Option list.

A.      

It is part of the postcode of the Peutz-Jeghers Society

B.      

It is the name of the gene most commonly associated with PJS

C.      

It is the Ornithological Society’s code for the Orkney Skua

D.      

Somatic mutations have been found in cervical cancer

E.       

None of the above

 

13. Tranexamic acid.

Tranexamic acid.

This topic featured in the exam in 2019.

Abbreviations.

GOH:         Goh E et al: “Perioperative management of women on oral anticoagulants and antiplatelet agents undergoing gynaecological procedures”.

TOG. 2020. Vol 22, Issue 2; Pages 131-6.

TA:             tranexamic acid.

Scenario 1.           

Which, if any, of the following describe the main mode of action of tranexamic acid? This is not a true EMQ as there may be more than one correct answer.

Option list.

A

inhibition of conversion of plasminogen to plasmin

B

inhibition of fibrinolysis

C

inhibition of factor Xa

D

inhibition of heparin activity

E

inhibition of plasmin activity

F

promotion of conversion of fibrinogen to fibrin

G

promotion of conversion of prothrombin to thrombin

H

promotion of platelet activation

I

promotion of platelet production

Scenario 2.           

Which, if any, of the following statements are true in relation to GOH?

Option list.

A

GOH says that TA should be considered when an apixaban antagonist is required

B

GOH says that TA should be considered when a clopidogrel antagonist is required

C

GOH says that TA should be considered when a factor Xa agonist is required

E

GOH says that TA should be considered when a factor Xa antagonist is required

F

GOH says that TA should be considered when a heparin  antagonist is required

G

GOH says that TA should be considered when Protein C is deficient

H

GOH says that TA should be considered when Protein S is deficient

I

none of the above

Scenario 3.           

Which, if any, of the following statements are true in relation to TA? This is not a true EMQ as there may be more than one correct answer.

Option list.

A

TA is teratogenic in rats and should be avoided in the first trimester

B

TA has not been shown to be teratogenic and is safe to use in pregnancy

C

TA is excreted is contraindicated in breastfeeding as the levels equate to maternal levels

D

TA levels in breast milk are one hundredth of maternal levels

E

none of the above.

Scenario 4.           

Which, if any, of the following statements are listed by eMC as contraindications?

Option list.

A

asthma

B

barbiturate use

C

consumption coagulopathy

D

convulsions

E

severe renal impairment

 

14.        Glucose-6-phosphate dehydrogenase deficiency.

Abbreviations.

G6PD:             glucose-6-phosphatase deficiency

G6PDD:          glucose-6-phosphate dehydrogenase deficiency           

Scenario 1.           

What is G6PDD? There is no option list.

Scenario 2.           

What categories are applied to G6PDD by the WHO? There is no option list.

Scenario 3.           

What other names are commonly used for G6PDD? There is no option list.

Scenario 4.           

Which, if any, of the following statements are true in relation to G6PDD?

Option list.

A

it is the most common enzyme defect in humans

B

it is the most common RBC enzyme defect in humans

C

it is the most common cause of neonatal jaundice

D

it is the most common cause of sickling crises

E

is a glycogen storage disorder

F

most of those with G6PDD have chronic anaemia

Scenario 5.           

Approximately how many people are affected by G6PDD worldwide?

Option list.

A

1,000 million

B

800 million

C

600 million

D

400 million

E

100 million

F

50 million

G

20 million

H

10 million

I

none of the above

Scenario 6.           

Which population has the highest prevalence of G6PDD?

Option list.

A

American Amish

B

Asians

C

Ashkenazi Jews

D

Eskimos

E

Irish Travellers

F

Kurdistan Jews

G

Sub-Saharan Africans

H

Turks

I

Uzbekistan albinos

J

None of the above

Scenario 7.           

Which, if any, of the following is the mode of inheritance of G6PDD?

Option list.

A

autosomal dominant

B

autosomal recessive

C

mitochondrial pattern

D

X-linked dominant

E

X-linked recessive

F

Y-linked

Scenario 8.           

Approximately how many mutations of the G6PDD gene have been identified? There is no option list.

Scenario 9.           

Which, if any, of the following is the mode of inheritance of G6PD?

Option list.

A

autosomal dominant

B

autosomal recessive

C

mitochondrial pattern

D

X-linked dominant

E

X-linked recessive

F

Y-linked

Scenario 10.        

Which foodstuff can trigger haemolysis in G6PDD and gives us one of the alternative names for the condition? What is the common name for the foodstuff? Which pest particularly attacks it? There is no option list.

Scenario 11.        

Which, if any, of the following drugs may cause haemolysis in those with G6PDD?

Option list.

A

aspirin

B

diphenhydramine

C

nalidixic acid

D

nitrofurantoin

E

paracetamol

F

phenytoin

G

sulphamethoxazole

H

trimethoprim

 

15.        Caldicott Guardian.

Question 1.

Lead-in

Which of the following statements is true of the Caldicott Guardian?

Option List

A

it is a large lizard, unique to the Galapagos Islands

B

it is the Trust Board member responsible for child safeguarding procedures

C

it is the Trust Board member responsible for complaint procedures

D

it is the person in a Trust responsible for patient confidentiality in relation to information

E

it is the person within a Trust responsible for dealing with bullying

Question 2.

Lead-in

The Caldicott Report identified 6 basic principles. What are they?

Option list.

There is none. Imagine that there is information about you stored on the computers of the local NHS Trust. What conditions would you want to lay down about sharing of that information within the Trust, with other NHS organisations and with non-NHS organisations?

Question 3.

Lead-in

The Caldicott Report made numerous recommendations. Which was particularly important for major NHS organisations such as Trusts?

Option List

A.      

the need to appoint a Caldicott Guardian

B.      

the need to create a Caldicott Register

C.      

the need to create a Caldicott Police Department

D.      

the need to create a link between the Caldicott Department and the DOH

E.       

none of the above.

Question 4.

Lead-in

What is the definition of the key role deriving from the answer to question 3?

Option List

There is none lest it give you the answer to question 3!

.

 

 

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