L5 Normal and Disordered Foetal Growth Flashcards

1
Q

How are small-for-GA babies classified?

A
  • Normal small fetuses: no structural abnormality, normal umbilical artery Doppler and liquor -> Not at risk, no special care needed
  • Abnormal small fetuses: chromosomal/structural abnormalities -> specialised care and counselling
  • Growth restricted fetuses: placental dysfunction, necessitating treatment and careful timing of delivery
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Define ‘small for gestational age’:

A
  • Fetus is within 10th weight percentile for its age (in weeks)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Define intrauterine growth restriction:

A
  • Fetus is unable to achieve its genetically predetermined size
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What qualifies as low birth weight?

A
  • Less than 2500gms
  • Baby could be SGA or could simply pre born prematurely
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What percentage of SGA babies are considered normal vs ‘at-risk’?

A
  • 40% healthy, 40% growth restricted
  • Those that are actually healthy should not be subjected to risky protocols or risk iatrogenic prematurity
  • Only the growth-restricted fetuses are at risk of potentially preventable perinatal death
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How is FGR classified and what contributes to each?

A
  • Symmetrical or asymmetrical
  • Related to underlying cause of growth delay and the duration of the insult
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Describe symmetrical FGR:

A
  • Fetal head and body are proportionately small
  • Fetal insult occurring during early development, impacting growth processes and cell hyperplasia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe asymmetrical FGR:

A
  • Fetal brain disproportionately large compared to liver (ratio >6)
  • Fetal insult during later development -> distinct growth patterns by differential impacts on axial and peripheral skeletal growth
  • Potential link to brain sparing effect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the brain sparing effect?

A
  • Blood flow prioritised to brain over other areas during development
  • Response to placental insufficiency
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What groups of risk factors exist for FGR?

A
  • Maternal (age, height, genetics, other conditions, lifestyle etc)
  • Placental and cord abnormality
  • Fetal factors (often congenital)
  • Infections (TORCH, malaria)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What lifestyle factors can increase risk of fetal growth restriction? (x3)

A
  • Drug use/abuse: marijuana, opiates, cocaine, smoking, drinking, chemotherapy, and others
  • Under/overnutrition
  • Altitude
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

List some placental and cord abnormalities:

A
  • Incorrect cord insertion
  • Single umbilical artery
  • Placental tumour
  • Circumvillate placenta
  • Defective trophoblastic invasion/placentation
  • Reduced blood flow to placental bed e.g. preeclampsia
  • Vascular anomalies e.g. TTTS
  • Decreased functioning mass: Small placenta, abruption, placenta praevia, post term pregnancy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Give examples of infections that are risk factors for FGR:

A
  • TORCH
  • TB
  • Malaria -> can invade placenta and damage its function
  • Parvo virus B19
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the underlying mechanism of IUGR?

A
  • Insufficient gas exchange and nutrient delivery to fetus
  • Often as a result of reduced capacity to carry/deliver/recieve oygen
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What factors can cause placental damage?

A
  • Smoking
  • Thrombophilia
  • Autoimmune diseases
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What factors can reduce oxygen carrying capacity of the mother?

A
  • Cyanotic heart disease
  • Smoking
  • Haemoglobinopathy
17
Q

What factors can impair oxygen delivery to the fetus:

A
  • Diabetes with vascular disease
  • Hypertension
  • Autoimmune conditions
18
Q

Outline the thrifty phenotype hypothesis:

A
  • Nutritional insult during critical period of gestation may permanently impact the child
  • Maternal nutritional status can alter epigenetic state of fetal genome and imprint gene expression
  • Examples include development of T2DM, metabolic syndromes
19
Q

Why is timing so important in delivery of FGR babies?

A
  • Increased fetal morbidity and mortality -> 10x increase in late fetal deaths among very small fetuses
20
Q

List some perinatal implications of FGR:

A
  • Stillbirth (40% non-malformed stillbirths are SGA)
  • Prematurity -> nacrotizing enterocolitis, ischaemic bowel, thrombocytopenia, temperature instability, renal failure, metabolic problems
  • Asphyxia
  • Congenital malformations
21
Q

Long-term consequences of FGR: (mother)

A
  • Abnormalities of hypothalamic pituitary axis
  • Cardiovascular disease
  • Insulin resistance
  • Metabolic syndrome
22
Q

Long term consequences for FGR children:

A
  • LBW associated with high cholesterol
  • Associated with decresed stroke volume, abnormally globular ventricles, high BP, increased intima-media thickness
  • Other: Poor physical and intellectual performance by various metrics, behavioural problems
23
Q

How can aspirin improve outcomes of IUGR?

A
  • Prevents aggregation of platelets
  • Thinning of blood improves flow
  • Particularly useful in cases of preeclampsia
24
Q

Evidence for clinical examination of IUGR using symphysio-fundal height:

A
  • Poor sensitivity and specificity, not particularly fallible
  • Benefits from being cheap and quick, can be conducted by the midwife
  • Predictive value can possibly be improved using customisation of charts (age, ethnicity, weight and parity) -> improved sensitivity to detect SGA
25
Q

What aspects of fetal biometry might be measured to help diagnose SGA?

A
  • Biparietal diameter
  • Head circumference
  • Abdominal circumference
  • Femur length
  • Estimated fetal weight
  • Amniotic fluid volumes (via deepest vertical pocket)
26
Q

What surveillance is typically carried out for mothers at risk of FGR?

A
  • Serial scans
  • Antenatal cardiocography (CTG)
  • Amniotic fluid volume assessment
  • Umbilical doppler
  • Biophysical profile assessment
27
Q

What test is done on FGR neonates?

A
  • Ponderal index (relationship between height and weight) -> Low?
  • If low, can indicate hypoglycaemia, hyperbilirubinemia, necrotising enterocolitis, hyperviscosity syndromes
28
Q

How may FGR be prevented?

A
  • Known to be largely unpreventabe
  • Some evidence of benefit for…
  • LDA and miniheparin
  • Reducing smoking
  • Antibiotics to prevent UTIs
  • Antimalarial prophyaxis
29
Q

What is the key idea in fetal surveillance in cases of FGR:

A
  • Careful monitoring to time delivery
  • Waiting until risk of in utero demise outweighs risk of delivery and prematurity
30
Q

Define fetal macrosomia and LGA:

A
  • LGA: Above 90th percentile
  • Macrosomia: BW>4000g regardless of GA
31
Q

How common is macrosomia?

A
  • 9 - 10% neonates
  • Geographical variation -> potential genetic and envirnomnental factors
32
Q

List the key risk factors associated with macrosomia:

A
  • Obesity
  • Diabetes (GDM/T2DM)
  • Postterm gestation
  • Multiparity
  • Stature of parents
  • Advanced maternal age
  • Previous macrosomic infant
  • Ethicity
33
Q

What are the key complications associated with fetal overgrowth?

A
  • Maternal diabetes
  • Fetal demise
  • Birth trauma -> shoulder dystocia, nerve palsies
  • Neonatal hypoglycaemia
34
Q

What is the greatest risk factor for macrosomia?

A
  • Maternal hyperglycaemia
  • Accelerates fetal growth
  • Alters body proportions