IUGR Flashcards
What are the risks of IUGR?
- increased risk of: hypothermia, hypoglycemia, pulmonary hemorrhage, infection, encephalopathy, NE
- asphyxia, meconium aspiration, MR
- operative delivery
- higher risk of stillbirth
What are the types of IUGR?
- type I - symmetrical IUGR <28 weeks
- type II - asymmetrical IUGR >28 weeks
What are the causes of symmetric IUGR?
fetal causes (20%)
- structural or chromosomal abnormalities (trisomy 13, 18, 21)
- Dwarf syndrome: Osteogenesis imperfecta
- Congenital malformation: structural defects
- early congenital/fetal infections: TORCH
What are the risk factors for chromosomal anomalies?
- 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
What are the infections that lead to symmetric IUGR?
Viral
- Rubella
- Cytomegalovirus
- hepatitis
- varicella
- influenza
Bacterial
- Listeriosis
- TB
- Syphilis
Protozoal
- toxoplasmosis
What are the causes of asymmetric IUGR?
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
What are the types of placental & cord abnormalities?
- placental abruption
- extensive infarctions
- placental calcifications
- true knots
- marginal & velamentous insertion of the cord
How will diagnosis of IUGR be suspected in ANC visits?
1- Poor maternal weight gain
2- uterine fundal heights (if < 2 cm from expected height)
How is diagnosis of IUGR diagnosed using ultrasound assessment?
1- abnormal BPD & abdominal circumference
2- associated oligohydramnios
3- accelerated placental aging
How is detection of CFMF diagnosed?
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)
How is assessment of fetal wellbeing done?
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)
How is IUGR managed?
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