RANZCOG q Flashcards

1
Q

a. Describe the relationship between zygosity and chorionicity in twin pregnancy. (3 marks, diagrams are acceptable)

A
Zygosity = number of fertilized ova resulting in pregnancy
Monozygous = 1 egg, 1 sperm, 1 zygote that subsequently splits to create twins
Dizygous = 2 eggs, 2 sperm, 2 zygotes
Chorionicity = number of chorion – placenta and membranes
Monochorionic = 1 placenta
Dichorionic = 2 placentae

Dizygous twins always become dichorionic, diamniotic
Monozygous - depends on the stage of development at which inner cell mass divided
If division occurs:
<3 days – DCDA
4-7 days – MCDA
8 days of more MCMA

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2
Q

You see a 28 year old primigravid woman with light bleeding at 8 weeks gestation. An ultrasound shows she has dichorionic diamniotic twins.

b. Outline the key events you should recommend for antenatal care in this pregnancy. (5 marks)

A
  • Further history – LMP. Obstetric and general medical history.
  • Antenatal bloods – as per singleton
  • 1st trimester screening – as per singleton
  • Supplementation – high dose folate (5mg), iron and iodine
  • Counselling re: risks to mother and fetuses
  • Planning care – shared care - secondary care (obstetric) with midwife appropriate
  • Morphology USS 20/40 including detailed cardiac views
  • 4-weekly growth USS from 20/40, shorter intervals if abnormality detected
  • 28/40 – GTT, FBC and iron studies
  • Each visit – vigilance HTN/PET – BP and urine
  • Delivery planning – gestation depends on maternal and fetal wellbeing. Mode depends on presentation – appropriate to consider NVD if 1st twin cephalic and consider maternal wishes, recommend elective delivery by 38/40 if uncomplicated
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3
Q

She presents in spontaneous labour at 34 weeks gestation. (DCDA twins)

c. Discuss the steps you will undertake in preparing for and performing this particular delivery in order to optimise the outcome. (7 marks)

A

Planning

  • Determine presentation of 1st twin – if cephalic, reasonable to proceed with NVD.
  • Setting – timely access to obstetric/anaesthetic staff and operating theatre. Arrange in utero transfer if not suitable NICU/obstetric unit and birth not imminent (may consider short term tocolysis for transfer)
  • Inform NICU as twins and preterm
  • Ensure equipment
  • 1:1 midwifery care

Performing

  • IVL and FBC/G&S in early labour
  • Regular VE to ensure adequate progress
  • IV antibiotics intrapartum as preterm – GBS prophylaxis
  • Analgesia – Epidural recommended - if quick recourse to OT or internal manouvres required. Consider maternal wishes.
  • Syntocinon indications as per singleton
  • CEFM – ensure both twins monitored consider ARM and FSE of 1st twin if required

Delivery

  • Paediatric team at delivery
  • After delivery of 1st twin – USS available, use to determine position of T2
  • If cephalic – stabilize
  • If non-cephalic options are ECV/continue labour and IPV/breech extraction – try to avoid rupture of membranes until twin turned
  • Consider use of syntocinon to minimize inter-twin delivery interval
  • Quick recourse to operative delivery if abnormal CTG – risk 4-10%
  • When 2nd twin delivered, active management of 3rd stage and deliver placentae
  • Vigilance PPH

(Also- steroids and ?tocolyse)

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4
Q

February 2015: Question 3: Twin Pregnancy

a. Describe the different types of twin pregnancy and how they arise. Where relevant include descriptions of the embryological events and their timing (3 marks)

A

Monozygotic – arise from splitting of a single embryo (ie one egg, one sperm) – can be di- or monochorionic
o Dizygotic – arise when two eggs have each been fertilized by one sperm at the same time. Are always DCDA

o Dichorionic diaamniotic – either dizygotic (as above) or monozygotic splitting within first 3 days of fertilization. Each have a placenta and amniotic sac
o Monochorionic diamniotic – always monozygotic, splitting between 3-9 days. Share a single placenta, each have amniotic sac
o Monochorionic monoamniotic – always monozygotic, splitting between 9-12 days. Share a placeta and single amniotic sac
o Conjoined twins – always monozygotic, splitting after 12 days. Share a placenta and aminiotic sac and are joined (variable types)

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5
Q

b. Chorionicity is best determined by ultrasound:
i) Using what criteria? (2 marks)
ii) At what gestation? (1 mark)

A
o	Dividing membrane
o	Twin peak or lambda sign – DCDA
o	T sign – MCDA
o	DCDA usually thicker (>2mm) separating membrane
o	Number of placental masses

ii) 10-14/40

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6
Q

You are reviewing a 34 year old woman in her first pregnancy at 12 weeks gestation. She has had an ultrasound showing she has monochorionic diamniotic twins (MCDA) with no abnormal features detected at first trimester aneuploidy screening.

c. You explain that her pregnancy is at increased risk of complications similar to dichorionic twins but is also at risk of specific monochorionic complications.
i) Briefly discuss 3 specific complications of MCDA twin pregnancies that may occur in this woman (3 marks)

A
o	TTTS (15%)
o	Caused by inequal sharing of placental blood flow through unidirectional placental anastomoses causing one twin to become donor 
o	Classical type – TOPS (twin oligohydramnios/polyhydramnios sequence) -can cause growth restriction, oligohydramnios, absent bladder, abnormal umbilical artery dopplers in donor and polyhydramnios, cardiac dysfunction and cardiac failure (hydrops) in recipient. Usually occurs in 2nd trimester. Occurs in 10% MCDA.
o	TAPS (twin anaemia/polycythemia sequence) – very slow transfusion from donor to recipient, so lacks the amniotic fluid discordance and cardiac dysfunction, but can cause significant anaemia and polycythemia reflected by markedly discordant MCA PSV. More common later pregnancy, may not be detected until birth. Occurs in 5% MCDA, and 10% post laser for TOPS.

o TRAPS – Twin reversed arterial perfusion syndrome – 1 twin is acardiac or has non-functioning heart, and other twin becomes ‘pump’. Very poor outcome if untreated, as hydrops can occur in pump twin
o Significant risk >20% of cerebral palsy or other significant neurodevelopmental delay of surviving cotwin if death of the other, due to significant haemodynamic changes at the time of demise
o Discordant growth – usually due to unequal share of placenta and velementous cord insertion but without fluid shifts associated with TTTS. Significant if >25% discrepancy

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7
Q

ii) Outline your management of her pregnancy to enable you to diagnose and/or facilitate appropriate intervention for MCDA specific complications that may occur (5 marks)

A

o Care under specialist obstetrician, often MFM unit if available
o NT at 12/40 as aneuploidy and NTD screen but also as discordance of NT and CRL increases the likelihood of later diagnosis TTTS (but not diagnostic and insufficient predictive value to use as screening test for this)
o Detailed anatomy scan with good views fetal hearts
o Fortnightly USS from 16/40 for growth, liquor, presence fetal bladder, dopplers including UAPI.
MCA PSV – from 24/40

earlier diagnosis of TTTS and referral to specialist centre likely to improve outcomes
o Patient education to present immediately if sudden increase abdominal girth or breathlessness as signs of polyhydramnios, or signs of preterm labour
o Usually delivery by 36-37/40 due to increased risk of stillbirth despite intensive surveillance. Mode of delivery controversial. Depends on patient’s wishes, can have vaginal birth if twin 1 cephalic and no other obstetric indications CS
o Consider corticosteroids if preterm delivery

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8
Q

At 34 weeks gestation, both twins are cephalic and are appropriately grown with no growth discordancy. The mother has no pregnancy complications.

d. What is the specific fetal risk of vaginal twin delivery in this woman? (1 mark)

A

Acute transfusion in labour (occurs in up to 10%)

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9
Q

Diagnosis of TTTS

A

Quintero staging based on Discordancy of Amniotic fluid
• Stage 1
• <20 weeks Twin 1 DVP <2cm, Twin 2 DVP > 8cm
• >20 weeks Twin 1 DVP <2cm, Twin 2 DVP > 10cm
• Stage 2 Absent Bladder in Oligohydramnios twin
• Stage 3 Critical Dopplers in either twin
• Critical Dopplers = Umbilical artery Doppler absent or reversed
• Stage 4 Hydrops in either twin
Stage 5- death of 1 twin

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10
Q

Diagnosis of TAPS

A

• MCA PSV which are >1.5 MoM AND <1.0 MoM
• There is a risk of TAPS because of small anastomoses that may remain after laser
coagulation (may be right at the edge of the placenta)

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11
Q

Diagnosis of sFGR

A
  • EFW discordancy of >25% OR

* EFW of one twin < 10th centile

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12
Q

When to deliver?

  • DCDA
  • MCDA
  • MCMA
A
  • DCDA 37-38/40
  • MCDA 36-37/40
  • MCMA 32/40
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13
Q

Definition zygosity

A

Degree of genetic similarity between each pair

Dizygous- 2 eggs and 2 sperm, typically share approx 50% of genetic material

Monozygous- 1 egg fertilised by 1 sperm which then splits at some stage in early pregnancy

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14
Q

Definition chorionicity

A

No of placentae in the pregnancy

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15
Q

Risks of twin pregnancy

A
  • Fetal loss- 2% DCDA, 8% monochorionic
  • Anomaly
  • Preterm birth
  • PET
  • IUGR
  • GDM
  • Complicated delivery
  • Monochorionic: TTTS (10-15%), TAPS, TRAP, selective IUGR-
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16
Q

What is the risk of TTTS?

A
  • 10-15%
17
Q

When is TTTS most likely to occur?

A
  • 16-26/40
18
Q

Mortality rate of TTTS if untreated?

A

80-90%

19
Q

Definition of TTTS

A

one twin receives more blood flow than the other by virtue of unidirectional flow along connecting vessels

20
Q

Definition of TAPS

A

Part of the spectrum of conditions attributable to anastomoses on the placenta.

It usually occurs later in pregnancy and has a better prognosis.

Characterised by one twin being anaemic and one polycythaemic without the discordant amniotic fluid associated with TTTS

MCA PSV which are >1.5 MoM AND <1.0 MoM

21
Q

Cause of sFGR in MC twins?

A

Unequal sharing of the placental mass

EFW discordancy of >25% OR EFW of one twin < 10th centile

22
Q

USS features of chorionicity

A
  • DC: Lambda sign
  • Absence of lambda suggests MC
  • T sign- MC di amniotic - ‘thin line- showing 1 placenta with dividing line of 2 amnion
  • Absence of membranes = MCMA
23
Q

USS for DCDA

A

1st trimester: Dating, chorionicity <14/40, NT

Anatomy 18-20/40

Growth from 24/40 every 4/52 unless concern

24
Q

USS for MC twins

A

1st trimester: Dating, chorionicity <14/40, NT

Twice weekly from 16/40 to detect TTTS - LV and UAPI

Anatomy 18-20/40

From 24/40 include MCA-PSV

25
Q

Mode of delivery

A

Large canadian study compared elective CS to NVD

  • No improvement in perinatal morbidity/mortality with elective CS
  • 44% of those in NVD group required CS, a third of these were in labour
  • NVD if leading twin cephalic appropriate but centre needs access to CS services
26
Q

Managing delivery of twins

A

Preparation:

  • Discussion antenatally re MOD and risks
  • USS to confirm leading twin cephalic
  • Inform SMO and paeds unit
  • IVA and FBC/G+H
  • Inform theatres/anaesthetic team

In first stage of labour:

  • Continuous CTG- Ensure FHR separated, may need to use FSE for twin 1
  • Recommend epidural once labour established
  • May need to use syntocinon to augment

Second stage:

  • USS in room for presentation of second twin
  • Inform paeds
  • May need to use synto to augment after delivery of twin 1
  • Can perform ARM if FH engaged in pelvis
  • If twin 2 not cephalic- consider ECV vs internal podalic version

Third stage:
- Active third stage with 40IU synto, prepare for risk of PPH

27
Q

Criteria for NVD in twins

A

o Uncomplicated twin pregnancy from 32 week gestation.
o The leading twin is cephalic presentation
o The estimated fetal weight of the second twin is no more than 20% that of the presenting twin (especially if planning breech extraction of the second twin)
o The estimated fetal weight of the second twin is ≥ 1500g if breech extraction of the second twin is planned.
o Absence of other contraindications to vaginal delivery (e.g placenta previa)

28
Q

Definition of TRAP sequence

A

Acardiac twin (with usually no cardiac tissue) being perfused by the anatomically ‘normal’ pump twin through a large artery–artery anastomosis on the placental surface.

29
Q

A healthy 38 year old primigravid woman is found to have dichorionic diamniotic (DCDA) twins at her 10 week dating scan.
a. Explain the physiology relating to dichorionic diamniotic twinning. (1 mark)

A

Dichorionic- two placentas. Diamniotic- 2 amniotic sacs

Can MZ or DZ

Monozygotic or dizygotic
Dizygotic- 2 ova fertilised by 2 different sperm. Typically share approx. 50% of genetic material.
Monozygotic- 1 ovum fertilised by 1 sperm. Then fertilised ovum splits between day 0-3 and results in 2x fetuses with separate placentas and amniotic sacs.

30
Q

b. Evaluate the use of one (1) currently available Down syndrome screening test in the context of this twin pregnancy. (3 marks)

A

MSS1 (nuchal + maternal age + analytes- PAPP-A, hCG)
• NT is accurate in twin pregnancy as in singletons (75% for 5% FPR) and can provide individual risk of aneuploidy
• In DC twins each NT is comparted with serum analytes to give individual risks of aneuploidy (DR 90% for FPR 5.9%), in MC the NT is averaged and combined with serum analytes to give the same risk

NIPT
• Expensive

31
Q

She has a morphology scan at 19 weeks gestation that indicates both fetuses have normal biometry and structural anatomy. You are seeing her in the antenatal clinic to discuss these results and plan her on-going care.
c. Explain how the increased risks associated with her twin pregnancy would change your antenatal management beyond routine care. (5 marks)

A

Risks: increased risk of fetal loss- risk for DCDA twins is 2%, as a result important to closely monitor the pregnancy. Obstetrician lead care.

Specific risks for DCDA:

  • Fetal anomaly- anatomy scan result is reassuring
  • SGA/FGR – recommend growth scans every 4 weeks from 24/40- may need to increase frequency if concerns
  • Risk of PET: BP monitoring, be aware of sx of PET and check urine for proteinuria. If additional RF for PET consider use of aspirin
  • Risk of GDM therefore recommend completion of OGTT
  • Risk of preterm labour and PPROM- discuss signs and symptoms of both and when to contact midwife/obstetric team for assessment
  • Risk of more complicated delivery – need to meet certain criteria to aim for NVD, increased risk of manipulation in 2nd stage for 2nd twin with risk of EMCS therefore recommend early epidural, increased PPH risk. Delivery in hospital with access to obstetric team and theatre.
32
Q

A vaginal delivery has been planned as her pregnancy has remained uncomplicated and the first twin is cephalic. At 36 weeks she presents in spontaneous labour.
d. Justify your intrapartum management beyond routine care. (6 marks)

A
  • Assess whether she meets criteria for NVD:
    o USS to confirm leading twin cephalic
    o Second twin >1500g, and has to be less than 20% growth discrepancy between twins
    o No other contraindication to vaginal birth
    o Otherwise uncomplicated twin pregnancy
    o Discuss delivery and check documented antenatal discussion re delivery. Discuss risks and recommendations.
  • Management of first stage:
    o Inform Obstetric SMO, Anaesthetic team, paeds, theatres
    o IV access with G+H and FBC
    o Continuous CTG and assessment of progress at least four hourly. May need to use FSE to confirm FHR monitoring for twin 1. Split FHR.
    o Recommend early epidural
    o May need to consider augmentation with synto as more likely to have irregular contractions
    o USS for presentation on arrival
    o Prepare room for twin delivery – 2x resuscitaires
  • Management of second stage:
    o SMO present for delivery, call paeds, inform OT and anaesthetic team
    o USS in room to scan presentation for 2nd twin
    o Stabilise second twin after delivery of first
    o May need to perform internal podalic version or ECV.
    o Consider amniotomy of second twin once in pelvis
    o May need to augment with synto to reduce delivery time if contractions stop.
    o Rare but may need to perform EMCS for second twin if malpresentation or fetal distress
  • Management of third stage:
    o Active 3rd stage with infusion of 40 IU oxytocin
    o Prepare for risk of PPH