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.
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
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Constitutional SGA | Symmetrically small, normal Dopplers, small parents | Customised chart, serial growth |
| Incorrect dates | Early dating scan discrepancy | First trimester USS dating |
| Fetal anomaly | Structural abnormality, abnormal anatomy scan | Detailed anomaly USS |
| Chromosomal abnormality | Structural markers, early-onset symmetrical FGR | Karyotype/microarray (amniocentesis) |
| Congenital infection (CMV, toxo) | Symmetrical FGR, intracranial calcification, hepatosplenomegaly | Maternal 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 Finding | Surveillance Frequency | Delivery Timing |
|---|---|---|
| Normal | 2-4 weekly | By 37 weeks |
| Raised PI (>95th centile) | Twice weekly | 37 weeks |
| Absent EDF | Daily-twice weekly | 32-34 weeks |
| Reversed EDF | Daily + CTG | 30-32 weeks or immediately if >32 weeks |
ASPRE Trial Summary
| Feature | Detail |
|---|---|
| Population | 1,776 high-risk women |
| Intervention | Aspirin 150mg OD from 11-14 to 36 weeks |
| Result | 62% reduction in pre-eclampsia <37 weeks |
| FGR benefit | Significant reduction in associated FGR |