IUGR Flashcards

1
Q

What are the risks of IUGR?

A
  • increased risk of: hypothermia, hypoglycemia, pulmonary hemorrhage, infection, encephalopathy, NE
  • asphyxia, meconium aspiration, MR
  • operative delivery
  • higher risk of stillbirth
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2
Q

What are the types of IUGR?

A
  • type I - symmetrical IUGR <28 weeks
  • type II - asymmetrical IUGR >28 weeks
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3
Q

What are the causes of symmetric IUGR?

A

fetal causes (20%)
- structural or chromosomal abnormalities (trisomy 13, 18, 21)
- Dwarf syndrome: Osteogenesis imperfecta
- Congenital malformation: structural defects
- early congenital/fetal infections: TORCH

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4
Q

What are the risk factors for chromosomal anomalies?

A
  • maternal age > 35 years
  • history of previous child with chromosomal disorder
  • abnormal parent (carrier)
  • consanguinity (first cousins) -> risk 6%
  • presence of gene defects -> risk 50%
  • diabetic mothers
  • hemoglobinopathies
  • inborn error of metabolism
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5
Q

What are the infections that lead to symmetric IUGR?

A

Viral
- Rubella
- Cytomegalovirus
- hepatitis
- varicella
- influenza

Bacterial
- Listeriosis
- TB
- Syphilis

Protozoal
- toxoplasmosis

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6
Q

What are the causes of asymmetric IUGR?

A

Maternal disease (chronic causes of placental insufficiency)
1- inadequate maternal nutrition
2- decreased utero-placental blood flow: (HTN, DM vasculopathy, post-dated pregnancy)
3- decreased oxygen carrying capacity: (sickle cell, cyanotic heart defect)
4- Brain sparing effect -> decreased urine output -> oligohydramnios
5- vascular diseases
6- chronic renal diseases
7- chronic hypoxia: living at high altitudes or cyanotic heart disease
8- placental & cord abnormalities

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7
Q

What are the types of placental & cord abnormalities?

A
  • placental abruption
  • extensive infarctions
  • placental calcifications
  • true knots
  • marginal & velamentous insertion of the cord
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8
Q

How will diagnosis of IUGR be suspected in ANC visits?

A

1- Poor maternal weight gain
2- uterine fundal heights (if < 2 cm from expected height)

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9
Q

How is diagnosis of IUGR diagnosed using ultrasound assessment?

A

1- abnormal BPD & abdominal circumference
2- associated oligohydramnios
3- accelerated placental aging

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10
Q

How is detection of CFMF diagnosed?

A

1- screening tests (noninvasive)
- PGD
- maternal serum cell-free fetal DNA (10w)
- serum PAPP-A, hCG + fetal NT ultrasound (11-13w)
- quadruple test: AFP, hCG, Estriol, Inhibin-A (15-20w)

2- confirmatory tests (invasive)
- chorionic villous sampling: TA (14-16w) TV (11-13w)
- amniocentesis (14-16w)
- cordocentesis (20w)

3- Screening for TORCH antibodies
4- detailed anomaly scanning (18 - 20w)

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11
Q

How is assessment of fetal wellbeing done?

A

1- daily fetal movement count
2- non-stress test
3- oxytocin challenge test
4- biophysical profile
5- doppler study for UA & MCA -> high resistance in UA & low resistance in MCA (ominous sign)

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12
Q

How is IUGR managed?

A

1- Prevention
- stop smoking & alcohol with proper dietary intake & vitamins
- control underlying pathology
- low dose aspirin (100mg) + anticoagulants (APS)

2- Near term (37w)
- early delivery
- IOL + continuous CTG monitoring
- emergency CS

3- Remote from term (<37w)
- in cases with trisomy 13 or 18 -> TOP
- expectant management + corticosteroids + MgSO4
- if severe placental insufficiency (fetal distress) -> TOP

4- Care of newborn baby
- examine to rule out congenital anomalies & infections
- monitor blood glucose levels (hypoglycemia is common)
- care for hypothermia & hyperbilirubinemia

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