L3 Multiple Pregnancy Flashcards

1
Q

Define zygosity:

A
  • Original number of fertilised eggs
  • e.g. monozygous twins have split from one original egg
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2
Q

Define chorionicity:

A
  • Whether the placenta is shared or not
  • e.g. dichorionic twins do not share a placenta
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3
Q

Mono- vs diamniotic twins:

A
  • Diamniotic: both babies share the same amniotic sac
  • e.g. MCMA means monochorionic monoamniotic where everything is shared
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4
Q

What shape would you look for on an USS to distinguish chorionicity?

A
  • Lambda sign: dichorionic
  • T-shape: monochorionic
  • Other signals: Membrane thickness
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5
Q

At what points does monozygotic typically occur following fertilisation (and in what proportion)?

A
  • Days 0 -3: Splitting of morula, ~25%
  • Days 4 - 7: Split at hatching, ~75%
  • Days 7 - 14: Blastocyst splitting after implantation, 1 - 2%
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6
Q

Describe Helin’s law:

A
  • Rule of thumb for incidence of multiple pregnancies
  • 1 in 89^n-1 twins where n = parity
  • e.g. Twins 1 in 89 pregnancies where n = 2
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7
Q

How does incidence of dizygotic twins vary around the world?

A
  • 6 in 1000 in Asia
  • 10 -20 in 1000 in Europe/USA
  • 40 in 1000 in Africa (Highest in Nigeria)
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8
Q

List some key risk factors for DZ twins:

A
  • ART (ovarian stimulation, mET)
  • Maternal age
  • Parity
  • Genetics (multiple modes of inheritance described)
  • Dietary sources of oestrogen
  • Geography
  • Seasonal light
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9
Q

What is the logic behind most risk factors for DZ twins?

A
  • Multiple ovulation
  • Two eggs reaching maturity at the same time and being fertilised by 2 sperm
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10
Q

How did the sET policy in ART affect multiple births?

A
  • Aiming to reach a target of 10% multiple births
  • Policy implemented in 2007 (UK)
  • 13% elective single transfer in 1991 vs 75% in 2019
  • Foudn to have same pregnancy rate as mET but with lower multiple pregnancy rate
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11
Q

What is known about risk factors for MZ twins?

A
  • Mechanisms largely unclear
  • No natural animal models exist to study this type of twinning
  • Factors related to environment are likely to include hypoxia, delayed implantation and temperature
  • Definitely known to be more common with IVF -> potentially via disruption of ZP, temperature and blastocyst transfer stage
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12
Q

What complications can arise in cases of monochorionic twinning?

A
  • Twin-to-twin transfusion syndrome (TTTS)
  • Twin anaemia polycthaemia sequence (TAPS)
  • Twin reverse arterial perfusion sequence (TRAPS)
  • Selective fetal growth resriction
  • Cord entanglement (MCMA)
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13
Q

What complications can affect all types of twins?

A
  • Maternal: Anaemia, GTT (Diabetes), PIH/PET (hypertension), hyperemesis, PPH
  • Fetal: Stillbirth, preterm births, miscarriage (3x), growth restriction, fetal abnormalities
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14
Q

Clinical management of different types of twins (during gestation):

A
  • GA and chorionicity determined at 11-14w -> nomenclature assigned
  • All types: 12w NT scan
  • Scans 4 weekly for DCDA and 2 weekly for MCDA and MCMA
  • Surveillance should take place for TTTS as well as maternal risks
  • Regular growth scans
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15
Q

When might delivery be induced for different types of twins?

A
  • DCDA: 37 - 38 weeks
  • MCDA: 36-37 weeks
  • MCMA: 32 weeks
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16
Q

How is the risk of congenital abnormalities affected in twins?

A
  • Dichorionic: same risk as normal
  • Monochorionic: 2-3x increased rate of CAs (20% chance of both twins being affected)
  • Management depends on nature of abnormality
17
Q

What type of congenital abnormalities can be seen in monochorionic twins?

A
  • Malformations e.g. neural tube defects, congenital heart disease (possibly due to part of twinning process)
  • Disruptions (e.g. limb reduction defects)
  • Deformations (e.g. club foot, hip dysplasia) -> overcrowding
18
Q

How will twins typically be delivered:

A
  • MCMA: C-section at 32 weeks
  • MCDA/DCDA: Varies based on GA, evidence of fetal compromise, maternal history and preference
19
Q

What is TTTS?

A
  • Twin to twin transfusion syndrome
  • In monochorionic pregnancies, vascular anastomoses occur between the two ‘halves’
  • Some are bidirectional (A-A, V-V) and thus are superficial
  • Some are unidirectional (particularly worried about deep A-V anastomoses)
  • This transmits one-way flow from a donor to recipient twin
  • Occurs in 15% of monochorionic twins with dire consequences for both babies
20
Q

How is TTTS diagnosed?

A
  • USS (2 weekly from 16 weeks)
  • Looking at liquor volumes, stomach and bladders of babies, doppler, growth
  • Maternal: shortness of breath, increased abdominal girth
21
Q

How is TTTS graded?

A
  • Grades I to V increasing in severity
  • Lowest: Significant discordance in amniotic fluid volumes (specific threshold for DVP aka deepest vertical pocket) but normal doppler and donor bladder visible
  • Highest: One or both babies dead
  • Will typically be treated at grade I or II
22
Q

How is TTTS treated?

A
  • Fetoscopic laser ablation
  • Improved survival compared to amnioreduction
  • Ongoing USS monitoring after procedure
  • Delivery at 34 - 37 weeks
23
Q

What is TAPS?

A
  • Twin anaemia-polycythaemia sequence
  • Small a-v vascular anastomoses (can occur following laser for TTTS)
  • Results in anaemia-polycythaemia discordance without haemodynamic instability (i.e. imbalance in RBCs)
24
Q

How is TAPS screened and managed?

A
  • MCA peak systolic velocity
  • Management uncertain; expectant delivery, transfusion, selective fetocide, repeat laser
25
Q

What occurs in TRAPS?

A
  • Twin reversed arterial perfusion
  • One twin supports an abnormal heartless tissue mass (acardiac twin)
  • 1% monochorionic twins
  • Acardiac twin certain to die, pump twin at 50% mortality (heart failure, preterm birth, hypoxia)
26
Q

What are the risks to the remaining twin if one dies in utero?

A
  • 15% mortality
  • 26% neurological abnormality
  • 66% preterm birth
  • Essentially due to the survivor losing blood into the dying twin
27
Q

What are the risks associated with MCMA twins?

A
  • Very high risk; 60% overall survival rate
  • Occurs in 1% of all twins
  • Cord entanglement!
  • Delivery by CS at 32 weeks
28
Q

What are the neonatal morbidities associated with spontaneous preterm birth?

A
  • Acute: Respiratory, gastrointestinal, neurological
  • Chronic: neurodevelopment, mental, respiratory, growth