Diagnosis and Management of Small-
for-Gestational-Age Fetus and Fetal
Growth Restriction (FGR)
Presented by Dr. Riyam Kaur
Under the guidance of - Dr. Vettri Vignesh
Assistant Professor
INTRODUCTION
• Fetal growth restriction (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.
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
Epidemiology and Importance
Affects 5–10% 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.
.
Etiology of FGR
 Maternal: Hypertension, preeclampsia,
malnutrition, smoking.
 Placental: Infarction, abruption,
insufficiency.
 Fetal: Chromosomal abnormalities,
infections (TORCH).
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
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
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
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.
Terminologies – Symmetric vs 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
Diagnosis of Early-Onset FGR (<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
Type of FGR Solitary 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
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
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.
Demand–Supply Situation in FGR
 Normal Demand & Normal Supply:
• Normal fetal oxygenation & growth
 Low Demand State:
• Fetus reduces metabolism to survive hypoxia
Growth slows (adaptive response)
 Low Supply State:
• Placental insufficiency → decreased oxygen/nutrient
delivery
• Primary mechanism behind FGR
Early-Onset FGR Management
• Intensive Doppler surveillance.
• Antenatal corticosteroids < 34 weeks.
• Magnesium sulfate for neuroprotection <
32 weeks.
Gestational Age Surveillance Delivery 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
Late-Onset FGR Management
Late FGR 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 —
TRUFFLE Protocol Overview
• Combines DV Doppler and computerized
CTG for delivery timing.
• Delivery recommended for reversed UA
flow after 30 weeks.
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.
Mode of Delivery
• Early FGR: often cesarean due to
compromised fetus.
• Late FGR: trial of labor possible with close
monitoring.
Surveillance Frequency
• Normal Dopplers: every 2 weeks.
• Abnormal Dopplers: every 2–3 days.
• Hospital admission for reversed flow or
abnormal CTG.
Adjunctive Therapies
• Low-dose aspirin for prevention.
• Oxygen therapy not recommended.
• Nutritional supplements show limited
benefit.
Prognosis
• Dependent on gestational age at onset and
severity.
• Early detection and optimal timing improve
survival.
Postnatal Outcomes
• • FGR infants at risk for hypoglycemia,
hypothermia, and growth delay.
• • Long-term risk: metabolic and
cardiovascular diseases.
Follow-Up
• Pediatric growth and neurodevelopmental
monitoring.
• Parental counseling regarding long-term
risks.
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.
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.
THANK YOU

fetal growth restriction updated ppt 2.pptx

  • 1.
    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. .
  • 5.
    Etiology of FGR Maternal: Hypertension, preeclampsia, malnutrition, smoking.  Placental: Infarction, abruption, insufficiency.  Fetal: Chromosomal abnormalities, infections (TORCH).
  • 6.
    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.
  • 16.
    Demand–Supply Situation inFGR  Normal Demand & Normal Supply: • Normal fetal oxygenation & growth  Low Demand State: • Fetus reduces metabolism to survive hypoxia Growth slows (adaptive response)  Low Supply State: • Placental insufficiency → decreased oxygen/nutrient delivery • Primary mechanism behind FGR
  • 17.
    Early-Onset FGR Management •Intensive Doppler surveillance. • Antenatal corticosteroids < 34 weeks. • Magnesium sulfate for neuroprotection < 32 weeks.
  • 18.
    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.
  • 27.
    Follow-Up • Pediatric growthand neurodevelopmental monitoring. • Parental counseling regarding long-term risks.
  • 28.
    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.
  • 30.