Contact us.
If you want my versions of the answers, e-mail your answers to me. I'll then connect you to the answers, which are on Dropbox.
See "Contact us" above for my e-mail address.
If you want my versions of the answers, e-mail your answers to me. I'll then connect you to the answers, which are on Dropbox.
See "Contact us" above for my e-mail address.
25 August 2016.
80
|
EMQ. Puerperal mental illness
|
81
|
EMQ. Menopause. NG23. Definition & diagnosis
|
82
|
EMQ. Menopause. NG23. Management
|
83
|
SBA. Needle-stick and related injuries
|
84
|
SBA. Endometrial hyperplasia. GTG67
|
80. EMQ.
Puerperal mental illness.
Lead-in.
The following scenarios relate to puerperal mental
illness.
If I had put all the answers into the option list it
would have been enormous. So there are quite a few where you need to decide
what your answer would be. Opting for “none of the above” is not exercising
your brain – make sure you come up with an answer.
Option list.
a.
arrange admission to
hospital under Section 5 of the Mental Health Act
b.
send a referral letter
to the perinatal psychiatrist requesting an urgent appointment.
c.
send an e-mail to the
perinatal psychiatrist requesting an urgent appointment.
d.
phone the community
psychiatric team.
e.
phone the on-call
psychiatrist.
f.
arrange to see the patient
in the next ante-natal clinic.
g.
arrange to see the
patient urgently.
h.
send a referral letter
to the social services department.
i.
phone the fire
brigade.
j.
phone the police.
k.
there is no such
thing.
l.
4 weeks
m. 6 weeks
n.
12 weeks
o.
26 weeks
p.
1 year
q.
<1%
r.
1-5%
s.
5-10%
t.
10-20%
u.
25%
v.
50%
w. 60%
x.
70%
y.
80%
z.
True
aa. False
bb. none of the above.
Scenario 1
What is the internationally
agreed classification for postpartum psychiatric disease?
Scenario 2
What time limits does DSM-IV
use for postpartum psychiatric disorders?
Scenario 3
What time limits does ICD-10
use pro postpartum psychiatric disorders?
Scenario 4
What clinical classification
would you use in a viva or SAQ?
Scenario 5
What is the incidence of
suicide in relation to pregnancy and the puerperium?
Scenario 6
What are the main conditions
associated with suicide in pregnancy and the postnatal period?
Scenario 7
Most suicides occur in single
women of low social class who have poor education. True / False
Scenario 8
The preferred method of suicide
reported in recent MMRs was drug overdose. True / False.
Scenario 9
When are women with Social
Services involvement particularly at risk of suicide.
Scenario 10
Which women have the highest
risk for puerperal psychosis and what is the risk?
Scenario 11.
What is the risk of puerperal
psychosis for a primigravida with BPD?
Scenario 12
What is the risk of PP in a
woman with no history of psychiatric illness but who has a FH of PP?
Scenario 13
Should screening include the
identification of women with no history of psychiatric illness but who has a FH
of PP?
Scenario 14
What do the Confidential Enquiries into Maternal Deaths
say about the use of the term “postnatal depression”?
Scenario 15
Women with schizophrenia have a
≥ 25% risk of puerperal recurrence. True / False
Scenario 16
If lithium therapy for BPD is
stopped in pregnancy, there is an increased risk of severe puerperal illness.
True / False.
Scenario 17
You are the on-call SpR for obstetrics. A woman has just
had a normal delivery of a 30 week baby that requires resuscitation. The mother
says that the baby must be left alone and not resuscitated. The paediatric SpR
and midwives are uncertain about what to do. What action will you take?
Scenario 18
You are the on-call SpR for obstetrics. The midwife on
the postnatal ward phones for advice. A primigravida who delivered yesterday
has stated that the baby is not hers and is refusing to care for it. What
action will you take?
Scenario 19
You are the on-call Consultant in O&G. The community
midwife has phoned for advice. She was asked to visit a primiparous woman who
had a normal delivery seven days before. The husband reports that she has
struck him several times. The woman tells her that voices have informed her
that this man is not her husband and that she should drive him away in case he
rapes her. What action will you take?
Scenario 20
You are the on-call Consultant in O&G. The community
midwife has phoned. She has just been phoned by a woman who had a Caesarean
section for breech presentation four weeks ago. She has been told by God that
breech babies are the spawn of the Devil and she is going to the local
multi-storey car park to jump off with the baby so that the baby cannot grow up
and harm people and so that she cannot have more Devil babies. What action will
you advise?
81. EMQ. Menopause NG23. Diagnosis & definitions.
Abbreviations.
AFC: antral follicle count.
AMH: anti-Müllerian hormone.
POF: premature ovarian failure.
POI: premature ovarian insufficiency.
Question 1.
Which
adjective did NICE use in relation to ideal care in recommendation 1.1.1 of
NG23?
Option List
A.
|
best
|
B.
|
holistic
|
C.
|
individualised
|
D.
|
personalised
|
E.
|
privatised
|
Question 2.
What is
the average age at the menopause?
Option List
A.
|
49 years
|
B.
|
50 years
|
C.
|
51 years
|
D.
|
52 years
|
E.
|
53 years
|
Question 3.
What age limit is used for the diagnosis of premature
ovarian insufficiency?
Option List
A.
|
30 years
|
B.
|
35 years
|
C.
|
37 years
|
D.
|
40 years
|
E.
|
45 years
|
Question 4.
What is
the approximate incidence of premature ovarian insufficiency?
Option List
A.
|
0.1%
|
B.
|
0.5%
|
C.
|
1%
|
D.
|
2%
|
E.
|
5%
|
Question 5.
What is the definition of the perimenopause?
Question 6.
What is
the definition of the postmenopause?
Question 7.
What is
the definition of premature ovarian insufficiency?
Question 8.
A healthy
physics teacher of 35 is diagnosed as menopausal. There is no obvious
explanation. Which of the following conditions could be the undiagnosed hereditary
cause?
Option List
A.
|
Cystic
fibrosis carrier status
|
B.
|
Elliptocytosis
|
C.
|
Fragile X carrier status
|
D.
|
Galactosaemia
|
E.
|
Polycythaemia vera
|
Question 9.
A healthy
woman of 52 presents with amenorrhoea for 15 months and vasomotor symptoms. She
is not taking any drugs. What tests should be done to confirm the diagnosis of
the menopause.
Option List.
A.
|
FSH
|
B.
|
FSH & LH
|
C.
|
FSH & oestradiol
|
D.
|
AMH
|
E.
|
None of the above
|
Question 10.
A healthy
woman of 46 presents with vasomotor symptoms and irregular periods. She is not
taking any drugs. What tests should be done to confirm the diagnosis of the
menopause?
Option List.
A.
|
FSH
|
B.
|
FSH & LH
|
C.
|
FSH & oestradiol
|
D.
|
AMH
|
E.
|
None of the above
|
Question 11.
Which
tests does NICE say should not be used to diagnose the menopause and
perimenopause in women > 45 years?
List of possible investigations.
A.
|
AFCA
|
B.
|
MH
|
C.
|
CT scan of pituitary fossa
|
D.
|
inhibin A
|
E.
|
inhibin B
|
F.
|
oestradiol
|
G.
|
ovarian volume
|
H.
|
prolactin
|
I.
|
thyroid function tests
|
Question 12.
What does
NICE recommend with regard to the use of FSH in relation to diagnosis of the
menopause?
Question 13.
What does
NICE recommend with regard to the use of FSH in relation to diagnosis of the
perimenopause?
Question 14.
What does
NICE say about the cost of FSH assay?
Question 15.
Which of
the following statements, if any, are true in relation to the advice from NICE
about the diagnosis of the menopause?
Option List
A
|
diagnose
without lab tests in healthy women > 45 years with menopausal symptoms
|
B
|
diagnose
without lab tests in healthy women > 50 years with menopausal symptoms
|
C
|
diagnose
without lab tests in women > 50 years with amenorrhoea > 6/12 and not
taking hormones
|
D
|
diagnose
without lab tests in women > 55 years with amenorrhoea > 6/12 and not
taking hormones
|
E
|
diagnose
on symptoms without lab tests in women > 45 years who have had
hysterectomy and are not taking hormones
|
F
|
none of
the above
|
Question 16.
Which of
the following statements is true in relation to the advice from NICE about the
diagnosis of the perimenopause?
Option List
A
|
diagnose
without lab tests in healthy women > 45 years with menopausal symptoms
|
B
|
diagnose
without lab tests in healthy women > 50 years with menopausal symptoms
|
C
|
diagnose
without lab tests in women > 50 years with amenorrhoea > 6/12 and not
taking hormones
|
D
|
diagnose
without lab tests in women > 55 years with amenorrhoea > 6/12 and not
taking hormones
|
E
|
diagnose
on symptoms without lab tests in women > 45 years who have had
hysterectomy and are not taking hormones
|
F
|
none of
the above
|
Question 17.
What does
NICE recommend with regard to the use of oestradiol assay in relation to
diagnosis of the menopause and perimenopause?
Question 18.
What does
NICE recommend in relation to the diagnosis of POI?
Question 19.
NICE uses
the term “urogenital atrophy” for the changes that may accompany the menopause.
There is now a preferred term – what is it?
82. EMQ.
Menopause NG23.
Management.
This is a follow-on from the SBA on “Menopause. NG23. Diagnosis &
definitions”.
Abbreviations.
POF: premature ovarian
failure.
POI: premature ovarian
insufficiency.
SJW: St. John’s Wort.
Question 1.
What information should be given to menopausal women considering
treatment?
Option List
There is none: this could be an OSCE station with no option list and you
need to have the answers in your large brain.
Question 2.
How does NICE define “short-term” in relation to risks and benefits?
Option List
A
|
≤ 6 months
|
B
|
≤ 1 year
|
C
|
≤ 18
months
|
D
|
≤ 2
years
|
E
|
≤ 5
years
|
Question 3.
What
does NG 23 say about how information should be provided?
Option List
A
|
orally
|
B
|
orally and written
|
C
|
orally, written and using intranet
|
D
|
orally, written and using internet
|
E
|
in different ways
|
Question 4.
Lead-in. What symptoms does
NG23 include as associated with the menopause?
List of symptoms.
A
|
joint and muscle pain
|
B
|
menstrual cycle changes
|
C
|
mood changes
|
D
|
vaginal dryness
|
E
|
vasomotor symptoms
|
Question 5.
What
information does NG23 say should be given to women about the available types of
treatment for menopausal symptoms?
Question 6.
Which, if any, of the following are recommended in relation to review /
follow-up for short-term symptoms.
A
|
review each treatment at 3/12 for efficacy / tolerability
|
B
|
review annually once established on treatment
|
C
|
review every 2 years once established on treatment
|
D
|
use NICE chart for documenting efficacy
|
E
|
none of the above
|
Question 7.
Which, if any, of the following should be advised in relation to
starting / stopping HRT
A
|
unscheduled vaginal bleeding is common
|
B
|
unscheduled vaginal bleeding should be reported immediately
|
C
|
HRT should be stopped until unscheduled vaginal bleeding is
investigated
|
D
|
HRT is best stopped in a regime of gradual reduction
|
E
|
none of the above
|
Question 8.
A woman with a high risk of breast cancer due to being a carrier of a
BRCA1 mutation wishes to discuss HRT. Which of the following is true.
Option List
A
|
oestrogen-only HRT is safe for her to use in relation to breast cancer
risk
|
B
|
HRT
is contraindicated and should not be used
|
C
|
paroxetine
should not be used when taking tamoxifen
|
D
|
fluoxetine
is safe to use when taking tamoxifen
|
E
|
none
of the above
|
Question 9.
Lead-in. A woman has a
diagnosis of POI at the age of 35. She has no risk factors for oestrogen
therapy and there is no family history of note. She wishes to discuss HRT.
Which of the following are true and worthy of discussion.
Option List.
A
|
HRT or the COC protect against osteoporosis if taken to the average
age at the menopause
|
B
|
HRT
is less likely to be linked to the development of hypertension
|
C
|
combined
HRT and the COC are linked to an increased risk of breast cancer, but the
increase is small
|
D
|
contraception
is not needed when she has gone 12 months from the diagnosis of POI
|
E
|
none
of the above
|
Question 10.
Which, if any, of the following are true of transdermal oestrogen.
Option List.
A
|
transdermal HRT at standard doses ↑ the risk of diabetes, but < oral
HRT
|
B
|
transdermal
HRT at standard doses ↑ the risk of stroke, but < oral HRT
|
C
|
transdermal
HRT at standard doses does not ↑ the risk of VTE
|
D
|
VTE risk is less with transdermal HRT than oral
|
E
|
none
of the above
|
83. EMQ.
Topic. Needle-stick, sharps and related risks.
Abbreviations.
CMV: cytomegalovirus
GBCV: GB virus C
HAV: hepatitis A virus
HBV: hepatitis B virus
HCV: hepatitis C virus
HDV: hepatitis
D virus
SOE: significant occupational exposure to
blood-borne infective agent.
VL: viral load.
Question 1.
Approximately
how many SOEs are reported annually in the UK?
Option List
A
|
~ 100
|
B
|
~ 250
|
C
|
~ 500
|
D
|
~ 1,000
|
E
|
~ 5,000
|
Question 2.
Who was Ignac
Phillip Semmelweis?
Option List
A
|
the
person credited with demonstrating the infective nature of puerperal sepsis
|
B
|
the horticulturist who first grew the white flower
subsequently popularised in the musical, “The sound of music”, naming it
after his first wife, Eidel.
|
C
|
the person who first used antisepsis in aerosol form to
reduce the risk of infection during C.
section.
|
D
|
the inventor of catgut sutures
|
E
|
the inventor of the Dalkon shield
|
Question 3.
Why does
the name of Semmelweis’s colleague Kotecha live on in medical history?
Option List
A
|
he was
the first doctor to perform hysterectomy
|
B
|
he was the first doctor know to undergo transgender
surgery
|
C
|
he died of infection akin to puerperal sepsis after a
SOE
|
D
|
he performed the first successful repair of a 3rd.
degree perineal tear
|
E
|
none of the above
|
Question 4.
Which of
the following have been described as causing infection after a SOE.
Infective agents
1.
|
hepatitis
A virus
|
2.
|
hepatitis
B virus
|
3.
|
hepatitis C virus
|
4.
|
human T cell leukaemia virus
|
5.
|
malaria parasites
|
Option List
A.
|
1 + 2 + 3 + 4 + 5
|
B.
|
1 + 2 + 3 + 5
|
C.
|
2 + 3 + 4 + 5
|
D.
|
2 + 3 + 4
|
E.
|
2 + 3 + 5
|
Question 5.
Which are
the main causes of infection to cause concern in the UK in relation to SOEs?
Infective agents.
1.
|
hepatitis A virus
|
2.
|
hepatitis B virus
|
3.
|
hepatitis C virus
|
4.
|
HIV
|
5.
|
treponema pallidum
|
Option List
A.
|
1 + 2 + 3 + 4 + 5
|
B.
|
1 + 2 + 3 + 4
|
C.
|
1 + 2 + 3 + 5
|
D.
|
2 + 3 + 4 + 5
|
E.
|
2 + 3 + 4
|
Question 6.
Which
group features most in the list of those reporting SOEs?
Option List
A.
|
doctors
|
B.
|
midwives
|
C.
|
phlebotomists
|
D.
|
nurses
|
E.
|
other healthcare workers.
|
Question 7.
Which
clinical activity generates most SOEs?
Option List
A
|
acupuncture
|
B
|
assisting in the operating theatre
|
C
|
intramuscular drug / vaccine injection
|
D
|
subcutaneous drug / vaccine injection
|
E
|
venepuncture
|
Question 8.
Approximately
how many cases of HIV seroconversion after SOE were recorded in the UK between
2004 and 2013?
Option List
A
|
0
|
B
|
1
|
C
|
20
|
D
|
100
|
E
|
500
|
Question 9.
Rate the
following body fluids as: high or low risk in relation to infectivity.
Option List
A.
|
amniotic
fluid
|
|
B.
|
blood
|
|
C.
|
breast milk
|
|
D.
|
cerebro-spinal fluid
|
|
E.
|
faeces
|
|
F.
|
peritoneal fluid
|
|
G.
|
saliva
|
|
H.
|
urine
|
|
I.
|
urine – blood stained
|
|
J.
|
vaginal fluid
|
|
K.
|
vomit
|
Question 10.
Rate the
following types of contact with body fluids as:
high-risk
low-risk
minimal or zero risk
Answer
A.
|
exposure to faeces: not bloodstained
|
|
B.
|
exposure to saliva: not bloodstained
|
|
C.
|
exposure to urine: not bloodstained
|
|
D.
|
exposure to vomit: not bloodstained
|
|
E.
|
exposure via broken skin
|
|
F.
|
exposure via intact skin
|
|
G.
|
injury deep, percutaneous
|
|
H.
|
exposure via mucosa
|
|
I.
|
injury superficial
|
|
J.
|
needle not used on source’s blood vessels
|
|
K.
|
needle used on source’s blood vessels
|
|
L.
|
sharps old
|
|
M.
|
sharps recently used
|
|
N.
|
sharps with blood not visible
|
|
O.
|
sharps with blood visible sharps
|
Question 11.
Rate the
following types of sources of potentially infective body fluids as:
high-risk
low-risk
minimal or
zero risk
Answer
A.
|
infected but VL and treatment details unknown
|
|
B.
|
recent blood test negative for all relevant viruses
|
|
C.
|
source has known risk factors but recent tests negative
|
|
D.
|
viral status not known but source has known risk factors
|
|
E.
|
viral status not known but source has no known risk
factors
|
|
F.
|
VL detectable
|
|
G.
|
VL not detectable
|
|
H.
|
VL unknown but on treatment with good adherence
|
Question 12.
Approximately
how many cases of HBV seroconversion after SOE have been recorded in the UK
since 1997?
Option List
A.
|
0
|
B.
|
1
|
C.
|
20
|
D.
|
100
|
E.
|
500
|
Question 13.
Approximately
how many cases of HCV seroconversion after SOE have been recorded in the UK
since 1997?
Option List
A.
|
0
|
B.
|
1
|
C.
|
20
|
D.
|
100
|
E.
|
500
|
Question 14.
What is
the estimated risk of transmission of infection of HBV in a SOE involving
sharps in a patient +ve for HBe antigen?
Option List
|
1 in 2
|
|
1 in 3
|
|
1 in 30
|
|
1 in 300
|
|
1 in 1,000 or less
|
Question 15.
What is
the estimated risk of transmission of infection of HCV in a SOE involving
sharps?
Option List
|
1 in 2
|
|
1 in 3
|
|
1 in 30
|
|
1 in 300
|
|
1 in 1,000 or less
|
Question 16.
What is
the estimated risk of transmission of infection of HIV in a SOE involving
sharps?
Option List
|
1 in 2
|
|
1 in 3
|
|
1 in 30
|
|
1 in 300
|
|
1 in 1,000 or less
|
Question 17.
What is
the estimated risk of transmission of infection of HIV in a SOE involving
mucosal splashing?
Option List
|
1 in 2
|
|
1 in 3
|
|
1 in 30
|
|
1 in 300
|
|
1 in 1,000 or less
|
Question 18.
Which of
the following carries the highest risk of transmission of an infective agent
after a SOE.
Option List
A.
|
a bite
on the bottom by an HIV-infected patient who finds your buttocks irresistible
|
B.
|
deep injury from a scalpel wielded by a psychopathic
surgeon
|
C.
|
deep
needle-stick after venepuncture
|
D.
|
spitting by a patient with HIV
|
E.
|
splash SOE from beating a disagreeable patient round
the head with a frozen turkey because you are sick to death of their
whingeing and perennial misery
|
Question 19.
List the
steps you would take in relation to immediate first aid, including the things
that might be suggested but you know are contraindicated.
Question 20.
Which
tests should be performed on the source after obtaining consent?
List what
you think should be done.
Option List
A.
|
HBV
surface antigen
|
B.
|
HCV
antibody
|
C.
|
HCV RNA
|
D.
|
HIV
antigen and antibody (fourth generation HIV immunoassay)
|
E.
|
TTV
antibody
|
Question 21.
What
consent is required from the source individual?
Option List
A.
|
consent
to having the tests
|
B.
|
consent
to having the results given to the occupational health department
|
C.
|
consent
to having the results given to the person who sustained the SOE
|
D.
|
consent
to having the results given to the hospital’s legal team
|
E.
|
consent
to notifying the hospital staff if the results are +ve.
|
Question 22.
What tests
should be done on the person who has sustained the SOE and there is a
significant risk of infection?
Option List
A.
|
a
baseline sample should be taken and stored for possible future use
|
B.
|
HBV surface antibody
|
C.
|
HCV antibody
|
D.
|
HIV antigen and antibody
|
Question 23.
If there is
a significant risk of HIV transmission, which of the following statements are
correct in relation to when should PEP be given?
Option List
A.
|
before
the results of the tests done on the source are available
|
B.
|
after the results of the tests done on the source are
available
|
C.
|
as soon as is practical
|
D.
|
within 24 hours
|
E.
|
within 72 hours
|
Question 24.
What are
the recommended drugs for PEP in the UK?
Option List
A.
|
Kaletra (200 mg lopinavir and 50 mg ritonavir)
|
B.
|
Raltegravir
400 mg twice daily
|
C.
|
Rifampicin 450-600mg daily as a single dose
|
D.
|
Tenofovir
+ lamivudine or emtricitabine
|
E.
|
Truvada
(245 mg tenofovir disoproxil fumarate and 200 mg emtricitabine)
|
Question 25.
Which of
the following statements are correct in relation to PEP in early pregnancy
Option List
A.
|
PEP is
contraindicated until after 12 weeks
|
B.
|
PEP should be started as for the non-pregnant
|
C.
|
PEP should be started, but TOP should be offered
|
D.
|
PEP should be started, but not until the puerperium
|
Question 26.
Which of
the following statements is true in relation to reducing the risk of HCV
infection.
Option List
A.
|
HCV
vaccine is safe in pregnancy and should be offered immediately
|
B.
|
HCV vaccine is a live vaccine and contraindicated in
pregnancy
|
C.
|
acyclovir is an effective drug for prophylaxis
|
D.
|
there is no known effective prophylactic drug
|
E.
|
early treatment of HCV infection is effective, so SOE
staff should be closely followed up for evidence of infection.
|
84. SBA.
Endometrial hyperplasia.
Abbreviations.
BSO: bilateral salpingo-oophorectomy
c.f. compared with
EC: endometrial cancer
EH: endometrial hyperplasia
ES: endometrial surveillance
Question 1.
What is
the definition of endometrial hyperplasia?
Option List
F.
|
endometrial thickness ≥ twice that of proliferative endometrium
|
G.
|
endometrial thickness ≥ twice that of proliferative
endometrium in the absence of oestrogenic stimulation
|
H.
|
premenopausal
endometrial thickness ≥ 6 mm; postmenopausal thickness ≥ 4 mm.
|
I.
|
proliferation of endometrial glands with ↑ gland to
stroma ratio c.f. proliferative endometrium
|
J.
|
proliferation of endometrial stroma with ↑ stroma to gland
ratio c.f. proliferative endometrium
|
Question 2.
Approximately
how many cases of endometrial cancer are diagnosed annually in the UK?
Option List
|
≤ 1,000
|
|
1,000 - ≤
1,500
|
|
1,500 - ≤
3,000
|
|
3,000 - ≤
5,000
|
|
5,000 - ≤
10,000
|
Question 3.
Where does
endometrial cancer rank in the list of gynaecological cancers by incidence?
Option List
A.
|
1st.
|
B.
|
2nd.
|
C.
|
3rd.
|
D.
|
4th.
|
E.
|
5th.
|
Question 4.
Where does
endometrial cancer rank in the list of gynaecological cancers causing death?
Option List
A
|
1st.
|
B
|
2nd.
|
C
|
3rd.
|
D
|
4th.
|
E
|
5th.
|
Question 5.
What is
the prevalence of EH compared with that of EC.?
Option List
A.
|
~ ¼
|
B.
|
~ ½
|
C.
|
similar
|
D.
|
> double
|
E.
|
> treble
|
Question 6.
What
classification system does the RCOG recommend for EH?
Option List
A.
|
BSGE
2015 classification based on endometrial thickness
|
B.
|
FIGO 2000 classification based on risk of malignancy
assessment
|
C.
|
FIGO 2005 classification based on histological grading
|
D.
|
WHO 2014 classification based on endometrial thickness
|
E.
|
WHO 2014 classification based on cytological atypia
|
Question 7.
A
48-year-old woman presents with erratic bleeding and menopausal symptoms.
Endometrial histology shows hyperplasia with no cytological anomaly. What is
the risk of progression to endometrial cancer in the next 10 years?
Option List
A.
|
< 1%
|
B.
|
≤ 5%
|
C.
|
5% - ≤
10%
|
D.
|
10% - ≤
15%
|
E.
|
> 15%
|
Question 8.
A
48-year-old woman presents with menopausal symptoms. Endometrial histology
shows hyperplasia with no cytological anomaly. What is the chance of
spontaneous regression of the endometrial hyperplasia?
Option List
A.
|
< 1%
|
B.
|
1% - ≤
10%
|
C.
|
10% - ≤
15%
|
D.
|
15% - ≤ 25%
|
E.
|
> 25%
|
Question 9.
A
48-year-old woman presents with erratic bleeding and menopausal symptoms. An
outpatient endometrial sample shows atypical hyperplasia. What is her lifetime
risk of EC?
Option List
A.
|
≤ 5%
|
B.
|
5% - ≤
10%
|
C.
|
10% - ≤
25%
|
D.
|
25% - ≤ 50%
|
E.
|
> 50%
|
Question 10.
Which of
the following are risk factors for the development of endometrial hyperplasia?
Option List
A.
|
aromatase
inhibitors
|
B.
|
clomiphene
used for induction of ovulation
|
C.
|
continuous combined HRT
|
D.
|
obesity
|
E.
|
tamoxifen
|
Question 11.
Which, if
any, of the following should be used for the diagnosis of endometrial
hyperplasia?
Option List
A.
|
endometrial
histology
|
B.
|
CT scan
|
C.
|
hystero-salpingography
|
D.
|
MRI scan
|
E.
|
trans-vaginal ultrasound scan
|
Question 12.
Which of
the following are true of the management of endometrial hyperplasia without
cytological abnormality?
Option List
A.
|
identified
risk factors should be discussed with the woman
|
B.
|
observation with follow-up endometrial biopsies is
acceptable
|
C.
|
progestogens improve the chance of regression
|
D.
|
progestogen should not be used when women show no
regression after B
|
E.
|
progestogen should not be used when women have abnormal
bleeding
|
Question 13.
Which of
the following are true of the management of endometrial hyperplasia without
cytological abnormality?
Option List
A.
|
brachytherapy
is the recommended 1st. line treatment in the GTG
|
B.
|
cyclical
oral progestogen therapy is the recommended 1st. line treatment in
the GTG
|
C.
|
intra-cavity
methotrexate is the recommended 1st. line treatment in the GTG
|
D.
|
the COC
is the recommended 1st. line treatment in the GTG
|
E.
|
the
LNG-IUS is the recommended 1st. line treatment in the GTG
|
Question 14.
Which of
the following statements are true in relation to the management of endometrial
hyperplasia without cytological abnormality?
Option List
A.
|
treatment
should be for a minimum of 6 months
|
B.
|
women should be encouraged to continue with the LNG-IUS
for at least 3 years
|
C.
|
endometrial surveillance with biopsy should be provided
at a minimum of 12 monthly
|
D.
|
review schedules should be individualised
|
E.
|
two consecutive 6-monthly biopsies should be negative
before discharge is considered
|
Question 15.
Which of
the following are true in relation to hysterectomy as management of endometrial
hyperplasia without cytological abnormality?
Option List
A.
|
treatment
to achieve regression should be for at least 6 months before surgery is
considered
|
B.
|
treatment to achieve regression should be for at least 12
months before surgery is considered
|
C.
|
treatment to achieve regression should be for at least 24
months before surgery is considered
|
D.
|
recurrence of endometrial hyperplasia without
cytological abnormality after progestogen therapy is grounds for considering
hysterectomy
|
E.
|
hysterectomy should be recommended to the woman who
declines surveillance
|
Question 16.
Which, if any, of the following statements are
true in relation to women with endometrial hyperplasia without cytological
atypia for whom hysterectomy is being considered?
Option List
A.
|
post-menopausal
women should have bilateral salpingo-oophorectomy
|
B.
|
pre-menopausal women should have bilateral salpingo-oophorectomy
|
C.
|
bilateral salpingectomy should be offered to all women
not having BSO
|
D.
|
laparoscopic hysterectomy should be offered in
preference to abdominal
|
E.
|
the GTG uses the term “total hysterectomy” which is
really stupid
|
Question 17.
Which of
the following is true in relation to the management of atypical hyperplasia of
the endometrium?
Option List
A.
|
endometrial
ablation is satisfactory if ES can be done for at least 5 years
|
B.
|
brachytherapy is satisfactory if ES can be done for at
least 5 years
|
C.
|
hysterectomy ±
BSO or bilateral salpingectomy should be offered
|
D.
|
frozen section should be done at the time of
hysterectomy to determine the need for lymphadenectomy
|
E.
|
continuous oral progestogen therapy should given for at
least 12 months post-op
|
Question 18.
A woman
with atypical hyperplasia of the endometrium wishes to retain her fertility.
Which, if any of the following are true?
Option List
A.
|
endometrial
and ovarian cancer must be ruled out to start with
|
B.
|
the MDT should decide management after reviewing the
results of the histology, imaging and tumour markers
|
C.
|
the woman should be advised is that medical advice is
to have hysterectomy because of the risk of cancer
|
D.
|
the LNG-IUS is the first-line preference for
conservative management
|
E.
|
oral progestogens should not be used
|
F.
|
she should have at least one clear endometrial biopsy
before conceiving
|
G.
|
referral to a fertility specialist should be arranged
to discuss ART
|
Question 19.
What
follow-up should be offered to the woman with atypical hyperplasia of the
endometrium who wishes conservative management?
Option List
A.
|
surveillance
includes endometrial biopsy
|
B.
|
surveillance should be at intervals of not more than 6
months until 2 consecutive, clear biopsies have been obtained
|
C.
|
surveillance should be at intervals of not more than 3
months until 2 consecutive, clear biopsies have been obtained
|
D.
|
long-term follow-up after 2 consecutive, clear biopsies
have been obtained can be at 6 – 12 month intervals
|
E.
|
long-term follow-up after 2 consecutive, clear biopsies
have been obtained can be at 12 – 24 month intervals
|
Question 20.
A woman
who has had successful conservative treatment for atypical hyperplasia of the
endometrium wishes to go onto HRT. Which, if any, of the following are true?
Option List
A.
|
continuous
progestogen therapy is necessary regardless of the type or mode of
administration of oestrogen replacement
|
B.
|
LNG-IUS or depot progestogens are preferred to oral
therapy
|
C.
|
hysterectomy should be recommended if not already done
|
D.
|
six-months TV scans should be done for endometrial
thickness
|
E.
|
none of the above
|
Question 21.
Which, if
any, of the following are true in relation to the woman with endometrial
hyperplasia who has been treated for breast cancer and are taking tamoxifen or
aromatase inhibitors.
Option List
A.
|
she
should be informed that tamoxifen ↑the risk of endometrial cancer
|
B.
|
she should be informed that aromatase inhibitors ↑the
risk of endometrial cancer
|
C.
|
she should be informed that the LNG-IUS ↓ the risk of
endometrial cancer for women on tamoxifen
|
D.
|
she should be informed that the LNG-IUS ↓ the risk of
endometrial cancer for women on aromatase inhibitors
|
E.
|
she should be informed that the effect of the LNG-IUS on
the risk of breast cancer recurrence is unknown and that it is not
recommended as a result
|
Question 22.
A woman is
found to have endometrial hyperplasia on an endometrial polyp. Which of the
following are true of the best management?
Option List
A.
|
complete
removal of the polyp must be checked
|
B.
|
hysteroscopy and curettage must be done to check the
endometrium
|
C.
|
an LNG-IUS should be recommended
|
D.
|
hysterectomy should be recommended
|
E.
|
none of the above.
|