2. FETAL GROWTH
• Nearly 20% of the almost 4 million infants born in the United States
are at the low and high extremes of fetal growth.
• In 2010, 8.2% of infants weighed <2500gm at birth, whereas 7.6%
percent weighed >4000gm
3. • THREE PHASES:
1. 1ST
Phase
- occurs in the first 16 weeks,
- rapid increase in cell number
2. 2ND
Phase
- extends up to 32 weeks gestation
- includes cellular hypertrophy and hyperplasia
3. 3RD
Phase
- after 32 weeks
- most fetal fat and glycogen are accumulated
4. • Corresponding fetal-growth rates:
5gm/day at 15 weeks
15 to 20gm/day at 24 weeks
30 to 35gm/day at 34 weeks
5. • Factors affecting fetal growth
Insulin and IGF (IGF-I)
Adipokines (Leptin)
Adequate supply of nutrients
6. • Fetal growth based on birthweight vary with ethnicity and geographic
region
• Term infants average 3400g at sea level, 3200g at 5000 feet, and 2900g
at 10,000 feet
8. FETAL-GROWTH RESTRICTION
• Designated to low birthweight newborns who are SGA
• In 1967, Battaglia and Lubchenco classified SGA neonates as those
whose weights were below the 10th
percentile for their gestational age
• In 1977, Campbell and Thomas described the use of the
sonographically determined head to abdomen circumference ratio
(HC/AC)
• 2 types of growth restriction:
– Symmetrical
– Asymmetrical
9. SYMMETRICAL GROWTH
RESTRICTION
• Proportionally small
• An early insult could result in a relative decrease in cell number and
size
• Chemical exposure, viral infection or cellular development
10. ASYMMETRICAL GROWTH
RESTRICTION
• Disproportionately lagging abdomen
• Might follow a late pregnancy insult such as placental insufficiency
from hypertension
• Resultant diminished glucose transfer and hepatic storage would effect
cell size and fetal abdominal circumference would be reduced
• Such somatic growth restriction is proposed to result from preferential
shunting of oxygen and nutrients to the brain
• This allows normal brain and head growth, that is brain sparing
11. RISK FACTORS AND ETIOLOGIES
• Gestational weight gain and nutrition
• Social deprivation
• Vascular disease
• Renal disease
• Pregestational diabetes
• Chronic hypoxia
• Anemia
• APA syndrome
• Inherited thrombophilias
• In fertility
12. • Placental and cord abnormalities
• Multiple fetuses
• Drugs with teratogenic and fetal effects
• Maternal and fetal infections
• Congenital malformations
• Chromosomal aneuploidies
13.
14. DIAGNOSIS OIF FETAL-GROWTH
RESTRICTION
1. Uterine fundal height
- safe, inexpensive and reasonably accurate screening method
2. Sonographic measurements of fetal size
- the most common method identifying poor fetal growth is
estimation of weight using fetal biometric measurements
- FL is the easiest and the most reproducible
- BPD and HC are dependent on the plane of section and may be
affected by deformative pressures in the skull
- AC are more variable
15. 3. AFV measurement
- association between fetal growth restriction and
oligohydramnios has been recognized
4. Doppler velocimetry
- detected in peripheral vessels such as the umbilical and middle
cerebral arteries
- considered standard in the evaluation and management of the
growth restricted fetus
16. • FIGURE 44-8 Umbilical arterial
Doppler velocimetry studies,
ranging from normal to
markedly abnormal. A. Normal
velocimetry pattern with a
systolic to diastolic (S/D) ratio
of < 3. B. The diastolic velocity
approaching zero reflects
increased placental vascular
resistance. C. During diastole,
arterial flow is reversed
(negative S/D ratio), which is an
ominous sign that may precede
fetal demise.
17. PREVENTION
• Begins before conception, with optimization of maternal medical
conditions, medications and nutrition
• Ant-malarial prophylaxis
• Correction of nutritional deficiencies
• Accurate dating
• According to ACOG, if growth is normal during a pregnancy following
a prior pregnancy complicated by fetal growth restriction, Doppler
velocimetry and fetal surveillance are not indicated
• Prophylaxis with low dose aspirin beginning early in gestation is not
recommended because of its poor efficacy to reduce growth restriction
18. MANAGEMENT
• Patient counseling and prenatal diagnostic testing are indicated
• Antepartum fetal surveillance should include periodic Doppler
velocimetry of the umbilical arteries in addition to more frequent fetal
testing
• Pregnancies complicated by fetal-growth restriction and at risk for
birth before 34 weeks receive antenatal corticosteroids for pulmonary
maturation
19.
20. • Management of the near term fetus
– delivery of a suspected growth restricted fetus with normal
umbilical artery Doppler velocimetry, normal amnionic fluid
volume, and reassuring fetal heart rate testing can likely be deferred
until 38 weeks’ gestation
– recommend delivery at 34 weeks or beyond if there is clinically
significant oligohydramnios
– With a reassuring fetal heart rate pattern, vaginal delivery is planned
21. • Management of the fetus remote from term
– If growth restriction is identified in an anatomically normal fetus
before 34 weeks, and amnionic fluid volume and fetal surveillance
findings are normal, then observation is recommended
– As long as there is interval fetal growth and fetal surveillance test
results are normal, pregnancy is allowed to continue until fetal lung
maturity is reached
– Reassessment of fetal growth is typically made no sooner than 3 to
4 weeks.
– Weekly assessment of umbilical artery Doppler velocimetry and
amnionic fluid volume is combined with periodic non stress testing
22. • Labor and delivery
– a woman with a suspected growth-restricted fetus should undergo
“high-risk” intrapartum monitoring
– frequency of cesarean delivery is increased
24. FETAL OVERGROWTH
• infants exceeding the 90th
percentile for a given gestational week are
usually used as the threshold for macrosomia or large-for-gestational
age (LGA) birthweight
• ACOG concluded that the term macrosomia was an appropriate
appellation for newborns who weigh 4500 g or more at birth
25. RISK FACTORS
• Obesity
• Diabetes—gestational and type 2
• Postterm gestation
• Multiparity
• Large size of parents
• Advancing maternal age
• Previous macrosomic infant
• Racial and ethnic factors
26. MATERNAL AND PERINATAL
MORBDTY
• Increased cesarean delivery rate exceeding 50%
• Rate of shoulder dystocia s as high as 17%
• Increased rates of postpartum hemorrhage, perineal laceration, and
maternal infection
28. MANAGEMENT
• Prophylactic labor induction
– obviate further fetal growth and thereby reduce potential delivery
complications
– A review of early term births indicates that elective delivery before
39 weeks’ gestation does not improve maternal outcomes and is
associated with worse neonatal outcomes
– current evidence does not support a policy for early labor induction
before 39 weeks’ gestation or delivery for suspected macrosomia
29. • Elective CS
– The ACOG does not recommend routine cesarean delivery in
women without diabetes when the estimated fetal weight is < 5000
g
– in diabetic women with overgrown fetuses, such a policy of elective
cesarean delivery seems tenable
30. • Prevention of shoulder dystocia
– when fetal overgrowth is suspected, the obstetrician naturally seeks
to balance the risks to the fetus with maternal risks
– elective delivery for the fetus that is suspected to be overgrown is
inadvisable, particularly before 39 weeks’ gestation
– elective cesarean delivery is not indicated when estimated fetal
weight is < 5000 g among women without diabetes and < 4500 g
among women with diabetes
Notes de l'éditeur
Human fetal growth is characterized by sequential patterns of tissue organ growth, differentiation and maturation.
Fetal development is determined by maternal provision of substrate, placental transfer of these substrates and fetal growth potential governed by the genome. However, the precise cellular and molecular mechanisms by which normal fetal growth ensues are incompletely understood.