TextbookObstetrics & GynaecologyFetal Growth Restriction

Fetal Growth Restriction

Fetal growth restriction (FGR) is a pathological failure of the fetus to reach its growth potential, associated with significant perinatal morbidity and mortality, and requiring close surveillance.

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Key Facts

FGR affects approximately 3-8% of pregnancies and is a leading cause of stillbirth in the UK Defined as estimated fetal weight (EFW) or abdominal circumference (AC) <10th centile with evidence of pathological growth RCOG GTG 31 and NICE NG201 guide management and surveillance of small-for-gestational-age (SGA) fetuses Umbilical artery Doppler is the primary surveillance tool; absent/reversed end-diastolic flow (AREDF) is a critical finding Risk factors include pre-eclampsia, smoking, chronic hypertension, antiphospholipid syndrome, placental insufficiency Customised growth charts (GROW/INTERGROWTH-21st) improve detection of pathological SGA Aspirin 150mg from 12 weeks reduces FGR risk in high-risk women (ASPRE trial) Timing of delivery depends on Doppler findings: AREDF typically warrants delivery by 32-37 weeks depending on other parameters

Overview

Key Facts

Fetal growth restriction is a pathological condition where the fetus fails to achieve its genetically determined growth potential, usually due to placental insufficiency. It is distinct from constitutionally small-for-gestational-age (SGA) fetuses, who are small but healthy.

Epidemiology

  • SGA (<10th centile): approximately 10% of pregnancies by definition
  • True FGR: approximately 3-8% of pregnancies
  • Responsible for significant proportion of UK stillbirths (accounts for 30-50% of non-anomalous stillbirths)

Aetiology

  • Placental factors (most common): uteroplacental insufficiency, pre-eclampsia, placental infarction
  • Maternal factors: chronic hypertension, renal disease, autoimmune disease (SLE, APS), diabetes with vasculopathy, smoking, substance misuse, malnutrition
  • Fetal factors: chromosomal abnormalities (trisomy 13, 18, triploidy), congenital infections (CMV, toxoplasmosis, rubella), structural anomalies
  • Multiple pregnancy: particularly monochorionic twins (TTTS)

Pathophysiology

  • Abnormal placentation with inadequate trophoblastic invasion of spiral arteries
  • Increased vascular resistance in the uterine and umbilical arteries
  • Fetal circulatory redistribution: blood preferentially directed to brain, heart, and adrenals (brain-sparing effect)
  • Progressive deterioration: abnormal umbilical artery Doppler → abnormal MCA Doppler → abnormal ductus venosus → fetal compromise

Clinical Presentation

Clinical Detection

  • Symphysis-fundal height (SFH) measurement <10th centile or crossing centiles
  • Static or slow fetal growth on serial measurements
  • Reduced fetal movements (in advanced FGR)

USS Findings

  • EFW or AC <10th centile on customised chart
  • Crossing centiles (fall of ≥2 centile lines)
  • Reduced amniotic fluid (oligohydramnios)
  • Abnormal Doppler indices

Red Flags

  • Absent or reversed end-diastolic flow (AREDF) in umbilical artery
  • Abnormal ductus venosus Doppler (absent or reversed a-wave)
  • Reduced fetal movements
  • Concurrent pre-eclampsia features
  • Abnormal CTG (reduced variability, decelerations)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Constitutional SGASymmetrically small, normal Dopplers, small parentsCustomised chart, serial growth
Incorrect datesEarly dating scan discrepancyFirst trimester USS dating
Fetal anomalyStructural abnormality, abnormal anatomy scanDetailed anomaly USS
Chromosomal abnormalityStructural markers, early-onset symmetrical FGRKaryotype/microarray (amniocentesis)
Congenital infection (CMV, toxo)Symmetrical FGR, intracranial calcification, hepatosplenomegalyMaternal serology, amniocentesis PCR

Diagnosis / Investigation

Bedside

  • Symphysis-fundal height measurement at each antenatal visit from 24 weeks (plot on customised chart)
  • Blood pressure and urinalysis (exclude pre-eclampsia)
  • CTG from 26 weeks if FGR suspected

Bloods

  • FBC, U&Es, LFTs, uric acid (pre-eclampsia screen)
  • PlGF-based testing if <37 weeks (NICE NG133)
  • TORCH screen if symmetrical early-onset FGR (CMV IgM/IgG, toxoplasma, rubella)
  • Thrombophilia screen if recurrent FGR/pre-eclampsia

Imaging

  • Serial USS: EFW, AC, HC, FL; plotted on customised growth charts; repeat every 2-4 weeks
  • Umbilical artery (UA) Doppler: primary surveillance tool
    • Normal → reduced → absent → reversed end-diastolic flow
  • Middle cerebral artery (MCA) Doppler: low PI suggests brain-sparing redistribution
  • Ductus venosus (DV) Doppler: absent/reversed a-wave indicates cardiac decompensation (late finding)
  • Amniotic fluid assessment: oligohydramnios (deepest pool <2cm) worsens prognosis

Special Tests

  • Amniocentesis for karyotype/microarray if early severe FGR with normal Dopplers
  • Placental histology postpartum

Management

Non-pharmacological

  • Smoking cessation (most modifiable risk factor)
  • Monitor fetal movements (kick counting)
  • Reduce activity if severe FGR
  • Multidisciplinary surveillance with fetal medicine input

Pharmacological

  • Aspirin 150mg OD from 12 weeks in high-risk women (reduces FGR risk; ASPRE trial)
  • Antenatal corticosteroids: betamethasone 12mg IM × 2 (24h apart) if delivery anticipated <34+6 weeks
  • Magnesium sulphate: for neuroprotection if delivery anticipated <30 weeks (4g IV loading)
  • Optimise maternal conditions: antihypertensives for pre-eclampsia/hypertension

Surgical/Interventional

  • Timing of delivery guided by gestational age and Doppler findings:
    • Normal UA Doppler: delivery by 37 weeks
    • Abnormal UA Doppler (raised PI): delivery by 37 weeks with closer surveillance
    • AREDF: deliver from 32-34 weeks (after steroids); by caesarean section
    • Abnormal DV Doppler: deliver from 30-32 weeks
    • Abnormal CTG: immediate delivery at any gestation

Referral Criteria

  • EFW <3rd centile: refer to fetal medicine
  • Abnormal Doppler findings: fetal medicine review
  • Concurrent pre-eclampsia: obstetric medicine input
  • Recurrent FGR: thrombophilia/APS screening, preconception counselling

Prognosis

  • Perinatal mortality in FGR: 5-10 times higher than appropriately grown fetuses
  • Stillbirth rate: significantly increased, particularly with AREDF
  • AREDF: if delivery delayed beyond 34 weeks, perinatal mortality can reach 40%
  • Neonatal complications: hypothermia, hypoglycaemia, polycythaemia, NEC, IVH
  • Long-term: increased risk of cardiovascular disease, type 2 diabetes, and metabolic syndrome in adulthood (Barker hypothesis)
  • Recurrence risk: 15-25% in subsequent pregnancies; higher if associated with pre-eclampsia

Other Relevant Information

Doppler Surveillance Frequency

UA Doppler FindingSurveillance FrequencyDelivery Timing
Normal2-4 weeklyBy 37 weeks
Raised PI (>95th centile)Twice weekly37 weeks
Absent EDFDaily-twice weekly32-34 weeks
Reversed EDFDaily + CTG30-32 weeks or immediately if >32 weeks

ASPRE Trial Summary

FeatureDetail
Population1,776 high-risk women
InterventionAspirin 150mg OD from 11-14 to 36 weeks
Result62% reduction in pre-eclampsia <37 weeks
FGR benefitSignificant reduction in associated FGR