Foetal Growth Restriction Flashcards

1
Q

Define Fatal growth restriction (FGR)

A

Failure of the fetus to achieve its predetermined growth potential for various reasons

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2
Q

Define small gestational age (SGA)

A

Birth weight <10th centile

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3
Q

Describe low birthweight babies (growth restriction, delivery time, morbidity and mortality, pathology)

A

Most LBW neonates are NOT growth restricted
Many FGR babies are delivered prematurely
3-10 fold increase in perinatal morbidity and mortality
LBW, FGR and preterm delivery have closely associated pathologies

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4
Q

Which centile is the most sensitive

A

10th is the most sensitive

The tenth centile will capture all babies with FGR, but will also include those babies that are just small for gestational age, i.e. you get a number of false positives.

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5
Q

Which centile is the most specific

A

3rd is the most specific
All babies recorded using the third centile will have FGR, but some FGR babies may be missed, i.e you get a number of false negatives.

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6
Q

What is the difference between gestational age and foetal age

A

GA is 2 weeks greater than FA. FA starts post fertilisation

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7
Q

What are the consequences of Intrauterine growth restriction (IUGR)

A

it has serious consequences for babies who survive (most common factor in stillborn)
There is an increased risk of IUGR and intrauterine death (IUD) in mother’s subsequent pregnancy.

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8
Q

What are the maternal causative factors of FGR

A
Smoking 
Diabetes 
Anaemia 
<16 
>25
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9
Q

What are the foetal causative factors of FGR

A

Multiple pregnancy
Chromosome abnormality
Inborn errors of metabolism

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10
Q

When are ‘at risk’ patient screened and what makes them ‘at risk’

A

24 weeks

PAPP-A < 0.3 MoM (Pregnancy associated plasma proteinA)
POHxPET/FGR (past obstetric history of Preclampsia/ fetal growth restriction)

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11
Q

What is screened for in “at risk” pregnancies

A

Maternal systemic disease e.g. HT< renal, sickle
Uterine artery Doppler in 1st/2nd trimester (blood flow in uterine arteries -> find high resistance flow)
Serial foetal biochemistry.

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12
Q

Define pre-eclampsia

A

Multisystem disease that usually manifests as hypertension and proteinuria
BP > 140/90mmHg
Proteinuria > 0.3g/24hour (PCR>30)

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13
Q

How does pre-eclampsia lead to IUGR

A

Normal exchange of nutrients is not possible

Due to inappropriate spiral artery remodelling

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14
Q

What may constitute a bad obstetric history

A

Previous maternal hypertension
Previous FGR
Stillbirth
Placental Abruption

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15
Q

When is delivery aimed for

A

≥28 weeks

and / or ≥500g

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16
Q

Describe the timing of delivery in pregnancies complicated by FGR

A

Timing delivery in these pregnancies depends on balancing the risks to the fetus if it remains in utero and the hazards from the prematurity, which decrease as the gestation advances

17
Q

What is required if the baby is born less than 36 weeks

A

Corticosteroids

18
Q

Is late IUGR or early IUGR easier to manage

A

Late

Early IUGR: 1%, usually linked to maternal disease e.g. PEC, difficult to manage because of risk of prematurity

Late IUGR: 5-7%, rarely linked to PEC, difficult to differentiate from SGA, easily managed by delivery

19
Q

Describe the growth of the baby if a dating problem is the cause of SGA

A

Consistent growth

Normal dopplers and fluid

20
Q

Describe the growth of the baby if placental insufficiency is caused by a foetal problem

A

Reduction in AC/FL
Reduced liquor
Deranged doppler

21
Q

Describe the growth of the baby if SGA is caused by a foetal problem

A

Fetal abnormality