Diagnosis and Managementof Small-
for-Gestational-Age Fetus and Fetal
Growth Restriction (FGR)
Presented by Dr. Riyam Kaur
Under the guidance of - Dr. Vettri Vignesh
Assistant Professor
2.
INTRODUCTION
• Fetal growthrestriction (FGR) and small-
for-gestational-age (SGA) are major causes
of perinatal morbidity and mortality.
• Accurate diagnosis allows improved
monitoring and timing of delivery.
• Fetal growth depends on maternal,
placental, and fetal factors.
3.
Terminologies – SGA,AGA & FGR
SGA – Small for Gestational Age:
• EFW or AC <10th percentile
• One that has not acheived its growth potential
AGA – Appropriate for Gestational Age:
• EFW/AC > 10 th percentile.
FGR – Fetal Growth Restriction:
• Pathologic restriction of growth potential irrespective of
absolute size
• Often defined as EFW or AC <5th percentile
• Doppler abnormalities typically present
4.
Epidemiology and Importance
Affects5–10% of pregnancies-
• Associated with stillbirth, hypoxia, and
neurodevelopmental delay.
• Overall, growth-restricted
fetuses have a higher rate of conditions associated
with prematurity, experience worse
neurodevelopmental outcome and are at increased
risk of non- communicable diseases in adulthood,
such as hypertension, metabolic syndrome, insulin
resistance, Type-2 diabetes mellitus, stroke.
.
Doppler Indices –PI, RI, S/D
PI (Pulsatility Index):
• (Peak systolic – End-diastolic) / Mean velocity
Sensitive marker of placental resistance
RI (Resistance Index):
• (Systolic – Diastolic) / Systolic
S/D Ratio:
• Systolic velocity / Diastolic velocity
Increases when placental resistance rises
7.
Cerebroplacental Ratio (CPR)
How to Calculate CPR:
• CPR = MCA PI / UA PI
Interpretation:
• Low CPR indicates redistribution & fetal hypoxia
• CPR <5th percentile = abnormal
Clinical Use:
• Helps identify late-onset FGR
• •Guides timing of delivery
8.
Pathophysiology
Placental insufficiency
•leads to decreased uteroplacental flow
and decreased oxygen and nutrient delivery
Fetal hypoxia
• Chronic low oxygen leads to redistrubution of
blood flow
• Brain sparing - increased flow to brain , heart
and adrenals
• Oxidative stress
damages placental villi and worsens placental
function
9.
Doppler Studies
Umbilical artery(UA): Increased PI →
placental resistance.
• Middle cerebral artery (MCA): Decreased
PI → brain sparing.
• Ductus venosus (DV): Reversed a-wave
→ severe hypoxia.
10.
Terminologies – Symmetricvs Asymmetric
FGR
Symmetric FGR:
• Proportionate reduction in AC, HC, FL
• Early pregnancy insult (chromosomal, infection)
Asymmetric FGR:
• AC reduced more than HC (HC/AC ratio ↑)
• Late placental insufficiency
• Brain-sparing present
11.
Diagnosis of Early-OnsetFGR (<32 Weeks)
Ultrasound:
• EFW or AC <3rd–5th percentile
• Falling growth centiles
• ↓ AFI / oligohydramnios
Doppler Abnormalities:
• UA: ↑PI, absent/reversed EDF
• MCA: ↓PI (brain-sparing)
• •DV: ↑PI or reversed a-wave
12.
Type of FGRSolitary Criterion Contributory Criteria
(≥2 required)
Early-Onset FGR
(<32 weeks, no
congenital anomalies)
• AC or EFW <3rd
percentile OR
• UA AEDF (absent end-
diastolic flow)
• AC or EFW <10th
percentile
• UtA-PI >95th percentile
and/or UA-PI >95th
percentile
• Growth crossing >2
quartiles
Late-Onset FGR
(≥32 weeks, no
congenital anomalies)
• AC or EFW <3rd
percentile
• AC or EFW <10th
percentile
• AC/EFW drop >2
quartiles
• CPR <5th percentile or
UA-PI >95th percentile
13.
Severity Stage (Primary)Factors (Secondary) Factors
Stage I – Mild Placental
Insufficiency
• Mild placental
insufficiency
• UA ↑PI
• Normal MCA & DV
• Mild maternal anemia
• Low maternal weight
gain
Stage II – Severe
Placental Insufficiency
• UA high resistance /
absent EDF
• Early MCA redistribution
• Maternal malnutrition
• Low BMI
• Smoking/alcohol
Stage III – Pre-acidosis • UA reversed EDF ±
• DV early abnormal PI
• High-altitude hypoxia
• Short inter-pregnancy
interval
Stage IV – High Risk of
Acidosis
• DV reversed a-wave
• Severe placental
vascular disease
• Socioeconomic stress
• Moderate maternal
illness
15.
Biophysical Profile &CTG
• BPP assesses fetal tone, movement,
breathing, and amniotic fluid.
• BPP score can predict both fetal pH and
outcome
• CTG evaluates fetal heart rate variability.
Gestational Age SurveillanceDelivery Criteria
24–28 weeks • UA Doppler 2–3×/week
• MCA + DV weekly
• Daily CTG if abnormal
• Steroids + MgSO₄
• DV reversed a-wave
• Persistent late
decelerations
28–30 weeks • UA/MCA q2–3 days
• DV weekly
• Growth every 1–2
weeks
• UA reversed EDF
• DV abnormal/high PI
• Abnormal CTG/BPP
30–32 weeks • UA q2–3 days
• MCA + CPR weekly
• DV weekly
• Absent EDF (>30 wks)
• Reversed EDF
• Rising DV PI
19.
Late-Onset FGR Management
LateFGR is characterized by milder and more aspecific
placental lesions
Category Findings Management /
Monitoring
Timing of
Delivery
Umbilical Artery
Doppler
Normal / PI>95th 1–2 wk or weekly
Doppler
38–39 wk / 37 wk
CPR / MCA CPR<5th, MCA
PI<5th
Increase
surveillance
37 wk
CTG Normal/Abnormal
Dopplers
Weekly / twice
weekly
—
Growth Scan — Every 2 weeks —
20.
TRUFFLE Protocol Overview
•Combines DV Doppler and computerized
CTG for delivery timing.
• Delivery recommended for reversed UA
flow after 30 weeks.
21.
Timing of Delivery
•Based on gestation, Doppler findings, and
fetal well-being.
• Early FGR: delivery when DV abnormal or
reversed flow.
• Late FGR: induction at 37–38 weeks if
CPR abnormal.
22.
Mode of Delivery
•Early FGR: often cesarean due to
compromised fetus.
• Late FGR: trial of labor possible with close
monitoring.
23.
Surveillance Frequency
• NormalDopplers: every 2 weeks.
• Abnormal Dopplers: every 2–3 days.
• Hospital admission for reversed flow or
abnormal CTG.
24.
Adjunctive Therapies
• Low-doseaspirin for prevention.
• Oxygen therapy not recommended.
• Nutritional supplements show limited
benefit.
25.
Prognosis
• Dependent ongestational age at onset and
severity.
• Early detection and optimal timing improve
survival.
26.
Postnatal Outcomes
• •FGR infants at risk for hypoglycemia,
hypothermia, and growth delay.
• • Long-term risk: metabolic and
cardiovascular diseases.
SUMMARY
• FGR ≠SGA — pathologic vs physiologic
smallness.
• Doppler is cornerstone of diagnosis.
• Early vs late FGR differ in etiology and
management.
• Individualized delivery timing is crucial.
29.
References
• Lees CC,Stampalija T, Baschat AA, et al.
• Diagnosis and Management of Small-for-
Gestational-Age Fetus and Fetal Growth
Restriction.
• Ultrasound Obstet Gynecol 2020; 56: 298–
312.