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DOI: 10.1111/tog.

12567 2019;21:143–7
The Obstetrician & Gynaecologist
CPD
http://onlinetog.org

CPD questions for volume 21 issue 2

CPD credits can be claimed for the following questions 6. estrogen levels are low in women with
online via the TOG CPD submission system in the RCOG polycystic ovary syndrome. ThFh
CPD ePortfolio. You must be a registered CPD participant 7. levels of LH and follicule-stimulating
of the RCOG CPD programme (available in the UK and hormone will be low in affected women. ThFh
worldwide) in order to submit your answers. Please log in 8. anti-m€ ullerian hormone is an accurate marker
to the RCOG website (www.rcog.org.uk) to access your of ovarian reserve in affected women. ThFh
CPD ePortfolio.
With regard to the clinical presentations of patients with
Participants can claim 2 credits per set of questions if at
RED-S,
least 70% of questions have been answered correctly. At least
50 credits must be obtained in this way over the 5-year cycle. 9. menstrual disturbances (such as amenorrhoea,
CPD participants are advised to consider whether the articles oligomenorrhoea and dysmenorrhoea) are
are still relevant for their CPD, in particular if there are more common symptoms. ThFh
recent articles on the same topic available and if clinical 10. eating disorders should be actively
guidelines have been updated since publication. screened for. ThFh
Please direct all questions or problems to the CPD Office. 11. amenorrhoeic sportswomen continue to
Tel: +44(0) 20 7772 6307 or email: cpd@rcog.org.uk remain at a 2–4-fold increased risk of stress
The blue symbol denotes which source the questions refer fractures once menstrual function has
to including the RCOG journals, TOG and BJOG, and been restored. ThFh
RCOG guidance, such as Green-top Guidelines (GTGs) and 12. delayed menarche is particularly common
Scientific Impact Papers (SIPs). All of the above sources among athletes participating in aesthetic
are available to RCOG Members and Fellows via the sports that emphasise leanness. ThFh
RCOG website. 13. polycystic ovary syndrome is common in
RCOG Members, Fellows, Registered Trainees and affected sportswomen. ThFh
Associates have full access to TOG content via the TOG
Regarding management of sportswomen with RED-S,
app (available for iOS and Android).
14. elite sportswomen with formal eating
disorders should not be allowed to train or
TOG Sports gynaecology compete until treatment has been initiated and
healthy eating behaviour has resumed. ThFh
Regarding Relative Energy Deficiency in Sport (RED-S),
15. energy intake should be initially increased by
1. energy availability is determined by dividing between 500 and 800 kcal/day, with a target
energy expenditure by energy intake relative to body mass index of >20.0 kg/m2. ThFh
fat-free mass. ThFh 16. serial LH measurements are useful in
2. the ‘female athlete triad’ encompasses the inter- monitoring management. ThFh
relationship between energy availability, 17. the use of LH and human chorionic
menstrual function and bone health. ThFh gonadotrophin therapy should be avoided in
3. less than 10% of clinicians feel comfortable fertility treatment for sportswomen as they
treating amenorrhoeic athletes. ThFh are prohibited by the World Anti-
4. women who partake in sports that emphasise Doping Agency. ThFh
strength and power are more likely to suffer
Concerning urinary incontinence in sportswomen,
from RED-S. ThFh
18. it is more common during competition
With regard to the physiology of RED-S,
compared with during training. ThFh
5. luteinising hormone (LH) is produced in the 19. pelvic floor exercises are the mainstay
anterior pituitary gland. ThFh of treatment. ThFh

ª 2019 Royal College of Obstetricians and Gynaecologists 143


CPD

20. duloxetine should be offered for improved 14. combined continuous therapy has a lower risk
symptom control where pelvic floor exercises of endometrial cancer. ThFh
are ineffective. ThFh
Regarding bleeding and HRT,
15. up to 80% of women on combined
TOG Unscheduled bleeding with hormone continuous HRT will experience unscheduled
replacement therapy bleeding or spotting in the first 6 months
of treatment. ThFh
Regarding menopause,
16. NICE recommends reporting any unscheduled
1. it is defined by the World Health Organization bleeding if it occurs after the first 6 months
1996 declaration as the permanent cessation of of therapy. ThFh
menstruation resulting from the loss of 17. unscheduled or abnormal bleeding is responsible
ovarian follicular activity. ThFh for 25–50% of women stopping HRT. ThFh
2. it is the last menstrual bleed diagnosed
Regarding investigations and treatment for unscheduled
retrospectively after 1 year of amenorrhoea in
bleeding during HRT,
the absence of any pathologic disorder that
could be responsible for the amenorrhoea. ThFh 18. hysteroscopy with endometrial sampling
3. in the UK, the median age is 50.8 years. ThFh remains the gold standard for uterine cavity
4. follicle-stimulating hormone (FSH) is the first evaluation in the UK. ThFh
gonadotrophin to rise in the biological 19. using a cut-off reference of 5 mm endometrial
ageing process. ThFh thickness on transvaginal ultrasound, the risk
5. the findings of plasma estradiol below of endometrial cancer in postmenopausal
20 pg/ml (range 5–25 pg/ml) as well as an women decreases by 90% for those with
elevated FSH >100mU/ml are consistent with thickness < 5 mm, regardless of hormone use. T h F h
cessation of ovarian function. ThFh 20. endometrial biopsy has been shown to miss up
to 20% of focal lesions like
Regarding vasomotor symptoms and menopause, endometrial polyps. ThFh
6. the ‘domino effect’ of hormone replacement
therapy (HRT) refers to the reduction in
anxiety, depression and cognitive disorders TOG Surgical smoke – what are the risks?
by its positive impact on With regard to the components of surgical smoke,
vasomotor symptoms. ThFh
7. hot flushes occur in about 70–80% of women 1. most of it is water vapour. ThFh
who go through physiological menopause. ThFh 2. about 25% of the constituents
are carcinogenic. ThFh
Regarding osteoporosis and menopause, 3. carbon monoxide is a component. ThFh
4. the plume generated from electrocautery of
8. menopause predisposes to type 2 osteoporosis. ThFh
1g tissue is comparable to that from
9. postmenopausal osteoporosis is responsible
three cigarettes. ThFh
for fractures in one of every two
5. human papillomavirus (HPV) and HIV have
postmenopausal women. ThFh
not been identified in it. ThFh
Regarding postmenopausal HRT, With regard to surgical smoke particle size and
10. it increases muscle mass and concentration,
maintains strength. ThFh 6. particles of mean diameter >100 lm have
11. it is indicated as first-line in women with been shown to remain airborne. ThFh
premature menopause. ThFh 7. particles generated by electrosurgery have a
12. the National Institute for Health and Care mean diameter ≥0.35 lm. ThFh
Excellence (NICE) says the lowest effective 8. particles <10 lm in diameter are inhalable. ThFh
dose should be used for the shortest 9. particles <2.5 lm in size can penetrate
possible period. ThFh the alveoli. ThFh
13. combined continuous therapy is 10. the highest emission of surgical smoke is
recommended in perimenopausal women. ThFh from muscle. ThFh

144 ª 2019 Royal College of Obstetricians and Gynaecologists


CPD

Exposure to surgical smoke has been associated with, Regarding fertility in women with EOA,
11. throat irritation. ThFh 14. the trend towards older age at motherhood
12. seizures. ThFh is now reversing. ThFh
13. sneezing. ThFh 15. fertility is lost early in the process. ThFh
14. diarrhoea. ThFh 16. EOA is associated with increased miscarriagerisk. T h F h
15. eye pain. ThFh
Regarding IVF in women with EOA,
A standard surgical facemask,
17. the live-birth rate per frozen oocyte is
16. offers good protection against surgical smoke. ThFh currently around 5–6%. ThFh
17. will filter out particles <5 lm in diameter. ThFh 18. mild ovarian stimulation has been shown to be
18. is effective whether it is loose or tight fitting. ThFh superior to normal or high-dose stimulation
19. when worn for long durations is in terms of live-birth rates. ThFh
less effective. ThFh 19. dehydroepiandrosterone improves pregnancy
20. is less effective against surgical smoke than a rates during IVF in women in some cases. ThFh
high-filtration respirator. ThFh 20. few adjuvants have consistently been shown to
improve outcomes in women with low
ovarian reserve. ThFh
TOG Early ovarian ageing
Regarding normal ovarian ageing, TOG Maternal, fetal, and neonatal outcomes
associated with long term use of
1. oocytes reach a maximum number in utero at
corticosteroids during pregnancy
16–20 weeks of gestation. ThFh
2. follicle loss is primarily due to ovulation. ThFh Placental transfer of exogenous corticosteroids is,
3. environmental factors affect ovarian ageing 1. similar for different corticosteroids. ThFh
more than genetic factors. ThFh 2. affected by their pharmacokinetics
4. oocyte quality declines from 37.5 years of age. ThFh and pharmacodynamics. ThFh
5. menopause occurs once the ovarian follicle
numbers decline to around 1000. ThFh Placental 11b-hydroxysteroid dehydrogenase type 2
(11b-HSD2) enzyme,
Regarding early ovarian ageing (EOA),
3. is a complete barrier to the fetoplacental
6. women with the condition usually passage of exogenous corticosteroids. ThFh
present with oligomenorrhoea. ThFh 4. has a different metabolism profile for
7. anti-m€ ullerian hormone levels are a good endogenous corticosteroids compared with
predictor of time to pregnancy exogenous corticosteroids. ThFh
in natural conception. ThFh
8. women with poor response to ovarian Fetal plasma corticosteroid concentration is,
stimulation during in vitro fertilisation (IVF) 5. higher with maternal exposure to fluorinated
have a higher risk of early menopause. ThFh corticosteroids compared with
9. it is associated with increased risk of other corticosteroids. ThFh
cardiovascular disease. ThFh 6. comparable following maternal administration
With regard to the pathophysiology of EOA, of hydrocortisone and dexamethasone. ThFh

10. oocyte quality is relatively preserved compared Regarding antenatal corticosteroid therapy,
with oocyte quantity. ThFh 7. routine repeat courses are recommended to
11. it is recognised to occur either as a result of a enhance fetal lung maturation. ThFh
smaller follicle pool at birth or 8. there is a dose-dependent relationship
accelerated follicle loss. ThFh between cumulative antenatal corticosteroid
12. polycystic ovary syndrome is a risk factor. ThFh exposure and reduced fetal growth. ThFh
13. the in utero environment has been shown to 9. neonatal benefits include reductions in
affect the rate of ovarian ageing in respiratory distress syndrome, neonatal death,
later life. ThFh cerebroventricular haemorrhage and
necrotising enterocolitis. ThFh

ª 2019 Royal College of Obstetricians and Gynaecologists 145


CPD

10. hydrocortisone is a last-resort alternative when 7. when the woman experiences a late
betamethasone and dexamethasone are miscarriage. ThFh
not available. ThFh
With regard to massive perivillous fibrin deposition,
Betamethasone and dexamethasone, 8. it is seen in third-trimester placentas only. ThFh
11. are both fluorinated corticosteroids. ThFh 9. the placenta appears stiff with a
12. have 30–40-fold increased glucocorticoid yellowish colouration. ThFh
potency than cortisol. ThFh 10. it is associated with 13–50% of stillbirths. ThFh
13. are poor substrates for placental metabolism 11. there is a low rate of recurrence in
by the 11b-HSD2 enzyme. ThFh subsequent pregnancy. ThFh
14. have significant mineralocorticoid action. ThFh Concerning fetal thrombotic vasculopathy,
15. are considered ‘long-acting’ corticosteroids. ThFh
12. variations in umbilical cord anatomy are a
Considering maternal chronic use of systemic recognised association. ThFh
corticosteroids, 13. its prevalence is between 10% and 15%. ThFh
14. thrombophilia screening is indicated in those
16. no adverse effects have been reported in
for whom placental histology confirms
breastfed infants with use during lactation. ThFh
the diagnosis. ThFh
17. they are associated with an increased risk of
gestational diabetes. ThFh With regard to villitis of unknown aetiology,
18. they are associated with neonatal
15. it is a common finding in up to 15% of
adrenal suppression. ThFh
near-term placentas. ThFh
There is sufficient evidence to, 16. it is associated with an infectious organism in
most cases. ThFh
19. recommend withholding antenatal
corticosteroid therapy for neonatal benefit in Villous dysmaturity,
the presence of maternal use of corticosteroids 17. is associated with maternal diabetes. ThFh
on a chronic basis. ThFh
20. confirm the long-term safety of fetuses In chorioamnionitis,
exposed to chronic maternal corticosteroids. ThFh 18. microbial invasion of the amniotic cavity has
been shown to also occur through
intact membranes. ThFh
TOG Placental histopathological
19. acute onset has been shown to lead to
abnormalities and poor perinatal neurological morbidity in the neonatal period
outcomes in some cases. ThFh
With regard to sending placentas for examination, 20. the grade 1 (mild-to-moderate) histological
type is characterised by the presence of three
1. they should be stored at 8°C to enable proper or more chorionic micro-abscesses. ThFh
histopathological evaluation. ThFh
2. they should be fixed in formalin if cytogenetic
analysis is indicated. ThFh BJOGImproving the effectiveness of lifestyle
3. histology will yield vital information if there is interventions for gestational diabetes
severe fetal distress and unexpected admission prevention: a meta-analysis and
of the baby to the neonatal unit. ThFh meta-regression
4. relevant information and clinical details are
vital to interpret the placental With regard to gestational diabetes mellitus (GDM),
histology findings. ThFh 1. the global prevalence is higher than 10%. ThFh
2. regulating gestational weight gain, according
Placentas should be sent for histology,
to Institute of Medicine guidelines, has been
5. when there is unexplained polyhydramnios. ThFh shown to reduce risk of occurrence. ThFh
6. as the information sought from examination 3. risk prediction models provide a more
helps to improve the outcome in comprehensive evaluation of risk than body
subsequent pregnancy. ThFh mass index ThFh

146 ª 2019 Royal College of Obstetricians and Gynaecologists


CPD

Concerning lifestyle interventions, 2. is more prevalent in offspring born from


pregnancies in which the mother had
4. they do not reduce the risk of GDM in
pre-eclampsia. ThFh
pregnant women with normal body
3. progression is significantly accelerated in
mass index. ThFh
women with recurrent pre-eclampsia
5. exercise of moderate intensity for
compared with women with a single event of
50–60 minutes twice a week during pregnancy
pre-eclampsia and subsequent
is associated with a more than 20% reduction
uncomplicated pregnancy. ThFh
in GDM. ThFh
4. risk is high in women who have only one
With regard to systematic reviews and meta-analyses, pregnancy complicated by pre-eclampsia and
no subsequent pregnancies. ThFh
6. the same person should extract all data to
maintain consistency. ThFh Women with a history of pre-eclampsia,
7. I2 is used to measure the effect size of
5. have an up to five-fold increased risk of
an intervention. ThFh
cardiovascular disease. ThFh
8. forest plots are used to show the relative risk
6. have a higher risk of future cardiovascular
of individual studies and the overall results. ThFh
disease when pre-eclampsia is early in onset. ThFh
9. relative risk is used to describe the
7. can decrease the risk of cardiovascular disease
heterogeneity of studies. ThFh
by almost 14% through lifestyle interventions
10. funnel plots are used to measure
after pregnancy. ThFh
publication bias. ThFh
Risk factors for recurrence of pre-eclampsia include,
Reference 8. inter-pregnancy interval of less than 4 years. ThFh
9. increasing body mass index
Guo X-Y, Shu J, Fu X-H, Chen X-P, Zhang L, Ji M-X, Liu X-M, Yu T-T, Sheng J-Z,
Huang H-F. Improving the effectiveness of lifestyle interventions for between pregnancies. ThFh
gestational diabetes prevention: a meta-analysis and meta-regression. BJOG 10. fetal growth restriction in the
2019;126:311–20. index pregnancy. ThFh

BJOG Recurrence of pre-eclampsia and the


Reference
risk of future hypertension and
cardiovascular disease: a systematic review Brouwers L, van der Meiden-van Roest AJ, Savelkoul C, Vogelvang TE, Lely AT,
Franx A, van Rijn BB. Recurrence of pre-eclampsia and the risk of future
and meta-analysis hypertension and cardiovascular disease: a systematic review and meta-
analysis. BJOG 2018;125:1642–54.
Cardiovascular disease,
1. is currently the leading cause of death in
women worldwide. ThFh

ª 2019 Royal College of Obstetricians and Gynaecologists 147

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