RANZCOG q Flashcards

1
Q

A 19 year old woman is referred by the GP with vaginal bleeding in her first pregnancy. The pregnancy is unplanned and of uncertain gestation. Examination shows a 14 week size uterus. An ultrasound arranged by the GP is strongly suggestive of a complete molar pregnancy.

a. Outline the investigations required for this patient. (3 marks)

A

• Serum hCG
• Full blood count
• Group and screen
• Consider:
o Chest Xray if clinically indicated
o Renal function tests, electrolytes, liver function tests if dehydrated
o TFTs if features of hyperthyroidism presen

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2
Q

b. Describe the initial management and follow up you would put in place for her. (5 marks) (for complete molar, after initial diagnosis)

A

• Consent: surgery and blood products (higher risk given molar pregnancy)
• Surgical evacuation of the uterus by an experienced operator using a large suction curette
o Misoprostol safe for cervical ripening
o Avoid oxytocics until evacuation complete
o Send POCs for histology + ancillary testing

• Anti-D if Rh negative
• Follow-up:
o Histology 1 week
o hCG 1 week (give form to have weekly bloods)
o Early pregnancy clinic review once histology and hCG back
Advice to use barrier contraception until HCG negative

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3
Q

c. Histology confirms a complete molar pregnancy.

i) How would you explain the cause of molar pregnancy to this woman? (1 mark)

A

• Occur when sperm fertilise an empty egg (an egg that has no genetic material)
o Either two sperm or one sperm that divides fertilise the egg
• The empty egg contains no maternal DNA and a fetus cannot develop- so a normal pregnancy cannot result
• The cells that make up the placenta divide abnormally and rapidly, filling up the uterus

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4
Q

ii) What are the characteristic histopathological features? (1 mark)

A
Embryo/fetus absent 
Widespread villous oedema 
Trophoblastic proliferation and atypia
P57 immunostaining negative 
XX or XY on karyotype (no triploidy)
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5
Q

d. What is the long term risk associated with molar pregnancy? Outline the principles of its management. (3 marks)

A

Gestational trophoblastic neoplasia
• Metastatic workup:
o MDT review,
o Bloods: hCG, UEC, LFTs, tumour hCG, TFTs, G&H
o CT head/chest/abdo/pelvis
• Calculate WHO risk score based on antecedent pregnancy, age, interval months from antecedent pregnancy, pre-treatment hCG level, largest tumour size (cm), number of metastases, failed chemoX
• If WHO score <7 then low risk protocol with MTX chemotherapy plus folinic acid
• If WHO score >7 then high risk protocol with EMACO (actinomycin D, etoposide, MTX)
• ChemoX until normal hCG level, then further 3 cycles
• Monthly hCG for 12 months- not to conceive during this time

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6
Q

Her ß-hCG levels completely resolve after the affected pregnancy. What are the implications of a molar pregnancy for future pregnancies? (2 marks)

A
  • Fertility rate not affected
  • 1:70 risk of repeat molar pregnancy: early USS and hCG level following the completion of future pregnancies, regardless of outcome
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7
Q

A 20 year old primigravid woman presents to the early pregnancy assessment unit at 7 weeks amenorrhoea with a history of vaginal spotting over the last few days. A diagnosis of tubal pregnancy is made on the basis of a transvaginal scan which shows an empty uterus with a 2.5cm left adnexal mass with no visible heartbeat. There is a corpus luteum seen in the left ovary. Her serum quantitative hCG is 2000iu/l at presentation.

a. What information above informs you that expectant management is contraindicated in this woman? (1 mark)

A

HCG >1,000 - 1,500
Size of the adnexal mass

This is not a pregnancy of unknown location with hcg < 1000 that can be managed expectantly. Serum HCG 2000 with a confirmed left adnexal mass with an empty uterus on transvaginal scan confirming ectopic pregnancy therefore contraindicated for expectant management.

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8
Q

b. Discuss the clinical criteria for the medical management of ectopic pregnancy. In particular, comment on the information available and that which is not available in this scenario. (5 marks)

A
Available: 
hCG is < 5000
No intra-uterine pregnancy 
Size of ectopic is smaller than 35mm
No FHR seen 

Unavailable:
Haemodynamic stability
No significant pain
No significant free fluid on USS
Normal bloods (FBC, LFTs, renal function)
Information on ability to return for assessment on days 4 &7, access to phone, car and assessment unit
Suitability for surgery (other medical conditions, previous surgery)

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9
Q

c. Assuming she has no clinical contraindications, outline your approach to medical treatment for this patient. (6 marks) (medical rx for ectopic)

A

Give written information on methotrexate and ectopic pregnancy
Offer condolences and pregnancy loss counsellor
Explain risks (stomatitis, conjunctivitis, GI upset, blood dyscrasias, deranged LFTs) and benefits (avoid surgery and surgical morbidity) and sign a consent form
Investigations: FBC, LFTs, UEC, G&H
USS on day of MTX
MTX dose is 50mg/m2 so use nomogram to calculate accurate dose
Give MTX by deep IM injection with safety precautions as it is a cytotoxic medication
If Rh negative, give anti-D
Return on day 4 and 7 for hCGs
If fall in hCG <15% then give second dose of MTX
Otherwise continue to monitor hCGs weekly until negative via early pregnancy clinic
Advise: refrain from ETOH, sexual intercourse and folic acid until hCG is negative
Advise against conception until 3 months after MTX dose
Discharge with written information and safety advice

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10
Q

With respect to treating ectopic pregnancy in general, list the surgical options available and the indication for each approach. (3 marks)

A

Laparoscopy vs laparotomy
Laparoscopy preferred management if patient is stable and surgeon available as reduced hospital stay and pain, quicker recovery
Laparotomy required if haemodynamically unstable with ongoing bleeding and deemped to be fastest approach

Salpingectomy vs salpingostomy
Salpingectomy standard of care- removal of the abnormal tube
Salpingostomy- can be performed if the woman requests it and understands that there is a risk of persistent trophoblast and an increased risk of recurrent ectopic and it does not improve the rate of spontaneous conception compared to salpingectomy
.There is a 1:5 chance of treatment failure if salpingostomy performed. Need to repeat HCG weekly until negative.

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11
Q

A 24 year old woman presents at 8 weeks of amenorrhoea with a scan that concludes she has a missed miscarriage / early pregnancy loss.

In Australia and New Zealand, what transvaginal ultrasound criteria are used to diagnose “missed miscarriage” / “early pregnancy loss”? (3 marks)

A

Intrauterine mean sac diameter 25mm or larger and no visible fetal pole or yolk sac.

Crown-rump length 7mm or larger and no fetal heart pulsation seen over 30 second period.

If uncertain of above findings, no growth in MSD or CRL in 7 days.

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12
Q

She has an empty intrauterine gestation sac measuring 30mm. You are asked to counsel her with respect to her management options.

b. List three management options available for this woman, their respective success rates and rank the effectiveness of each option with respect to success of treatment for missed miscarriage / early pregnancy loss. A table may be used. (6 marks)

A

conservative/expectant mx, success rate 60% (rank 3)

medical mx with misoprostol- success rate 84% (rank 2)

surgical mx - success rate 97% (rank 1)

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13
Q

The randomised controlled Miscarriage Treatment Trial (MIST trial BMJ 2006) examined the risk of harm for each management option. Choose three outcome measures from this trial and outline the result obtained. (6 marks)

A

Primary outcome: gynaecological infection
No difference between groups

Secondary outcomes:
Duration of symptoms: earlier cessation of bleeding with surgical management
Pain: higher rates of extra analgesia and pain with expectant management
Unplanned admission and curettage: 50% expectant and 40% medical management
Blood transfusion: no statistically significant difference
Return to work: no difference
Anxiety and depression scores: no difference

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14
Q

A 32 year old woman presents with a history of three miscarriages (G3P0) within the last 2 years at 8, 9 and 8 weeks gestation respectively. No investigations have been performed. You are seeing her and her partner to discuss their management.
a. Describe and evaluate the four recommended investigations which may establish a cause for their recurrent miscarriage prior to another pregnancy. (8 marks)

A
  • USS pelvis: Evaluate uterine abnormalities as a cause eg uterine septum for recurrent first trimester miscarriage, bicornuate uterus second trimester
  • Parental karyotype: Evaluates for Robertsonian or balanced translocations as a cause for recurrent miscarriage- 3-5% couples with miscarriage
  • Antiphospholipid syndrome: Evaluates for antiphospholipid syndrome- thrombosis and pregnancy criteria plus lab evidence (she would have the clinical criteria based on her recurrent first trimester miscarriage): lupus anticoagulant, anti-cardiolipin, b2 glycoprotein 1 antibodies
    Abnormal on 2 occasions 12 weeks apart
    15% all women, can improve pregnancy rate with treatment with aspirin/heparin
  • Thrombophilia screening: 5% of women may have a hereditary thrombophilia- these have been implicated in recurrent miscarriage.
  • Cytogenetics on POC: Evaluate for aneuploidy and evidence of other single-gene disorders such as alpha thalassemia
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15
Q

History, examination & investigation did not determine a cause for their previous miscarriages. You are seeing the woman for a follow-up consultation.
b. Outline and justify four issues which are relevant to her next pregnancy. (4 marks)

A

• Early management should be in a recurrent pregnancy loss clinic as the prognosis for a successful future pregnancy is around 75% with supportive care alone
• Pregnancy vitamins: folic acid and iodine should ideally be taken 1-3 months prior to conception, she should continue these
• Vaccines: if she is rubella or hep B non-immune, she should be vaccinated
• No evidence for the use of:
o Aspirin and heparin
o Progesterone
• Obesity: advise weight loss and exercise to maximise physical condition for healthy pregnancy
• Psychological: offer support

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16
Q

Two randomized controlled trials (RCTs) of treatment using heparin and low-dose aspirin for unexplained recurrent miscarriage provide Level 1 evidence for pharmacological intervention.

c. With respect to one of these RCTs
i) Name the trial or its lead author. (1 mark)
ii) State the main conclusion of the trial. (1 mark)
iii) Identify one important weakness in the trial design. (1 mark)

A

SPIN:

  • No difference between intensive monitoring and intensive monitoring + aspirin + LMWH to improve pregnancy rates
  • Included women with 2 or more recurrent miscarriages- may have diluted effects for women with 3 or more

ALIFE

  • No difference between placebo, aspirin, or aspirin + LMWH to improve live birth rates in unexplained, recurrent miscarriage
  • LMWH not blinded
  • Included women with 2 or more recurrent miscarriages- may have diluted effects for women with 3 or more
17
Q

Outline the theoretical immunological mechanisms in the mother that allow implantation of the embryo to occur in normal pregnancy.

A

High level of the proinflammatory T helper (Th)-1 and cytokines (IL-6, IL-8, TNFα) characterizes early implantation
NK cells in human decidua have a role in regulating trophoblast invasion by the production of IL-8 and interferon-inducible protein-10 chemokines. Furthermore, decidual NK cells are potent secretors of an array of angiogenic factors that induce vascular growth that is essential for the establishment of an adequate decidua

18
Q

A 39 year old woman G3P0 presents at 8 weeks gestation with an ultrasound demonstrating a non-viable fetus. She has had two previous first trimester miscarriages.

Describe the relevant clinical features you would obtain from the history.

A

Current symptoms – pain, bleeding, fever
LMP
Menstrual history
Other gynae history – uterine malformations, smear history
Details of previous miscarriages – dates, gestations, nature (embryonic, non embryonic, molar etc) and requirement for D+C, any cause found (chromosomal examination etc)
Any investigations of miscarriage to date
PMHx (APLS, thrombophias), PSurgHx, FHx (thrombophilias, chromosomal problems)
Meds
Lifestyle factors – smoking, alcohol, drugs
Any relevant medical history of partner eg balanced translocations

19
Q

List the investigations you would offer the patient with a justification for each.
(for recurrent miscarriage)

A

Chromosomal examination of fetus +/- karyotype of woman and partner
Chromosomal cause for miscarriage common and increases with age
Parents may be phenotypically normal but have balanced translocation which may be a cause of recurrent miscarriage

Antiphospholipid screen – lupus anticoagulant, anticardiolipin antibodies (one of these positive over 2 tests 12 weeks apart + history of recurrent miscarriages fulfills diagnostic criteria)
Affects 15% of women with recurrent miscarriages
Treatment available with heparin and aspirin

Thrombophilia screen – Factor V Leiden, activated Protein C resistance, antithrombin III
Cause of recurrent miscarriages
Also has implications for health with risk of VTE

Pelvic USS for uterine malformations
Suitable first screen for abnormalities, may require further investigation with saline sonohysterography or hysteroscopy
Resection of uterine septum can improve live pregnancy rates for women with recurrent miscarriage

20
Q

Discuss the pharmacology of mifepristone and misoprostol that enables them to act synergistically to achieve a medical termination of pregnancy. (4 marks)

A

• Mifepristone is an anti-progesterone and misoprostol is a prostaglandin E1 analogue and a naturally occuring uterotonic
• Mifepristone is given 24-48 hours and competitively inhibits natural progesterone, increasing the sensitivity of the myometrium to prostglandins by five times
o Maximal effect on uterine contractility and cervical ripening seen at 36-48 hours
• The combination of the two agents are the best regimen for medical termination and are 95% effective up to 9 weeks
o 200mg mifepristone and 800mcg misoprostol buccally
 Best route of administration for misoprostol is bucally or vaginally- more effective with a lower chance of systemic side effects

21
Q

The Management of miscarriage: expectant, medical or surgical? Results of randomised controlled trial (miscarriage treatment (MIST) trial) Trinder J. et al 2009 is a RANZCOG Landmark Trial.

b. With respect to the MIST Trial:
i) Outline the intervention in each of the three (3) arms of the trial. (3 marks)
ii) State the result of the primary outcome measure. (1 mark)
iii) Outline two (2) statistically significant advantages of surgical management for early fetal demise. (2 marks)

A

Expectant management- no intervention
Medical management:
Incomplete miscarriage: single PV dose of 800mcg misoprostol
Missed miscarriage: oral 200mg mifepristone then admitted to hospital for PV dose of 800mcg misoprostol
Surgical evac offered if expulsion didn’t occur within 8 hours of misoprostol
Surgical management: admitted to hospital for suction curettage under GA

ii) No difference between the groups in the rates of gynaecological infections

iii) Earlier cessation of bleeding (but no change in Hb or haematocrit)
Lower rates of unplanned hospital admissions
Lower rates of unplanned surgical curettage

22
Q

You are seeing a 23 year old woman at 10 weeks gestation with an incomplete miscarriage on ultrasound scan. She is having minimal bleeding. After discussion of her options her preference is to go home without any intervention. She is provided with the contact details of her closest hospital Emergency Department prior to leaving the Early Pregnancy Assessment Unit.
c. Discuss the information you give her regarding expectant management in this situation with reference to the results and discussion from the MIST trial (see above). (5 marks)

A

In the MIST trial, 80% of women completed their miscarriage over 3 days in the expectant management group
In women who choose expectant management with an incomplete miscarriage:
30-50% will have an unplanned admission due to an emergency or changing their minds about their method of management
20% will have an unplanned curettage
40% will need additional pain relief
There is no difference after miscarriage with regards to return to work, sick leave, psychological outcomes, or restrictions on activities of daily living
There is no increased risk of infections with expectant management
Women who are suitable for expectant management:
Women who have car and a phone
Women with 24 hour access to the emergency department
Women who will not be home alone but will have support and assistance through the process
When safety advice has been given

23
Q

A primigravid woman presents at 7 weeks gestation with persistent nausea and occasional vomiting which is affecting her quality of life. She has been given dietary and lifestyle advice and now seeks information about alternative therapies that evidence has shown to be effective for nausea in pregnancy.
Outline the protocols for 3 different alternative therapies effective for nausea and vomiting in pregnancy. (3 marks)

A

Ginger – The use of ginger products may be helpful to women but the evidence of effectiveness was limited and not consistent, though two recent studies support ginger over placebo.
Powdered ginger 1-1.5g divided over 24hrs, or ginger containing foods or ginger supplements.

Acupressure and acupuncture some evidence to show a slight reduction in nausea and vomiting but results mixed. However in absence of harm and strong placebo effect, patients may benefit from trial of acupressure wrist bands.

Vitamin B 12 – reduce nausea but not effecting for vomiting.

24
Q

At 9 weeks gestation she is admitted to hospital with hyperemesis gravidarum (HG).
Justify the initial investigations you will organise. (6 marks)

A

Weight – for baseline and to monitor of improvement or exacerbation over time.

MSU (for Ketones, WCC and specific gravity and culture): Assess for infection and ketones to assess dehydration and also for monitoring of improvement

Bloods (Urea and electrolytes, creatinine, liver function test, TFT’s) – assess for electrolyte abnormalities, renal impairment from dehydration. LFT’s – AST, ALT can be raised in hyperemesis, TFT’s if history of underlying thyroid abnormalities or other signs of hyperthyroidism, it can also be raised with high hcg from thyroid stimulation, FBC – can show increase in haematocrit with dehydration)

Pelvic ultrasound scan (Viability and to assess for molar pregnancy, multiple pregnancy and also assess for theca lutein cysts associated with molar pregnancies)

25
Q

List 8 severe maternal complications that may result from inadequately treated HG. (4 marks)

A

Short term severe outcomes:

Micronutrient deficiency
Wernickes encephalopathy from vitamin B1 deficiency
Rare bleeding disorder or embryopathy from vitamin K deficiency
Malnutrition causing
immunosuppression,
poor wound healing and
muscle wasting
Oesophageal tears ( Mallory Weiss ) , oesophageal rupture
Hepatic insufficiency
Acute tubular necrosis
Osmotic demyelination syndrome ( formerly known as central pontine myelinolysis )
Psychosocial and social dysfunction
VTE

26
Q

Discuss 2 postulated theories regarding the cause of HG in this woman. (2 marks)

A
  1. hCG and biochemical hyperthyroidism
    Raised level of hCG mimics TSH and causes raised thyroxine levels
    Level of hCG is directly correlated with vomiting and T4 level and inversely correlated with TSH levels
    Peak in hCG levels weeks 6-12 coincides with presentation of HG
  2. Physiological changes in GI tract
    Changes in oesophageal pressure, gastric peristalsis and stomach emptying from elevated oestrogen
27
Q

List the clinical features needed to make a diagnosis of hyperemesis gravidarum

A

Prolonged nausea and vomiting in pregnancy
Dehydration
Ketosis
Electrolyte disturbance (may or may not have)
Weight loss >5% body weight

28
Q

List the potential maternal complications of moderate/severe hyperemesis

A
Wernickes encephalopathy
Central pontine myelinolysis
Oesophageal rupture
Acute kidney injury from dehydration
Hypokalaemia
Hypernatraemia
Hypocholaemic alkalosis
VTE
Psychological consequences
29
Q

A 19 year old primigravida is admitted at 11 weeks gestation with intractable vomiting that has persisted over the previous five weeks. She has no previous history of any medical problems. On examination she is clinically dehydrated and tachycardic. Examination is otherwise normal. Blood has been sent for full blood count, urea and electrolytes, liver function tests and thyroid function test. The results from these are within normal limits except for:

Na 125 mmol/L (normal 135-145 mmol/L)
K 3.1 mmol/L (normal 3.5-5.0 mmol/L)
Urea 6.8 mmol/L (normal 2.5-6.7 mmol/L)
TSH 0.2 mU/L (normal 0.5-5.7 mU/L)
Free T4 25 pmol/L (normal 11.0-22.9 pmol/L)

Outline how you would manage this patient

A

Admit
IVF replacement
Normal saline + 30mml KCl initially to replace potassium, then plasmalyte (want to replace sodium more slowly)
Fluid balance
Fluid review after first 2-3L, likely to require more
Regular antiemetics dependent on local protocol, likely combination of:
Metoclopramide
Ondansetron
Cyclizine
Prochlorperazine
Pyridoxine
Thiamine – IV initially
Dietician input, daily weights
Monitor ketones
Arrange dating and viability scan
Ensure booking bloods done, started on iodine and folic acid
Ensure booked with LMC
No need to treat hyperthyroidism as likely self limiting biochemical hyperthyroidism that will resolve after 1st trimester once hyperemesis resolves – arrange followup TFTs in 6-8 weeks

30
Q

A primigravid woman presents at 7 weeks gestation with persistent nausea which is affecting her quality of life. She has already been given dietary and lifestyle advice and would like information about non-pharmacological interventions that may relieve her symptoms.
a. There is limited evidence from randomised controlled trials (RCT) to support the effectiveness of non-pharmacological intervention. List three (3) non-pharmacological interventions used for nausea and vomiting in pregnancy that have some RCT evidence of benefit, and describe how each is used/ administered. (3 marks)

A

Ginger
Powdered ginger 1-1.5g daily in divided doses
Can also be taken in food, in ginger tea or ginger beer

Acupressure
Applied by a band or a finger to the P6 point on the wrist
Some studies show benefit over placebo

Vitamin B6
25-50mg orally OD
Evidence for benefit for nausea, not for vomiting

31
Q

At 9 weeks gestation she is admitted to hospital with hyperemesis gravidarum (HG).
b. Name and justify the initial six (6) investigations you will organise. A table may be used for your answer. (6 marks)

A

USS
Dating of pregnancy, confirm viability, check if multiple or molar pregnancy

Electrolytes
Hyponatremia and hypokalaemia can occur due to dehydration and vomiting and need to be corrected

Renal function
Dehydration and vomiting can lead to renal impairment

FBC
Evaluate for anaemia, check haematocrit for haemoconcentration

Urine- MSU, ketones
UTI can cause and exacerbate nausea/vomiting
Point towards degree of dehydration and ketosis

LFTs
Severe hyperemesis gravidarum can cause deranged LFTs

Blood sugar
Rule out diabetic ketoacidosis