Gastrointestinal congenital anomalies requiring surgery
M R C O G PA R T 2 · S O S P O C K E T C A R D · K N O W L E D G E A R E A 5 – A N T E N ATA L C A R E
GI Congenital Anomalies Requiring Surgery: Diagnosis, Counselling & Management Mires S et al. Gastrointestinal congenital anomalies requiring surgery: diagnosis, counselling, and management. TOG 2023;25:186–195. doi:10.1111/tog.12884
6% ~10% 95.7% WHO GLOBAL CONGENITAL ANOMALY RATE OF ANOMALIES ARE GI ANTENATAL DETECTION, OMPHALOCELE
DO N' T-M IS S FA C TS
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Giant omphalocele = >5 cm diameter or >50% liver in sac – risk of pulmonary hypoplasia; consider ELCS to ↓dystocia/trauma
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Physiological gut herniation resolves by 12 weeks – scanning for omphalocele before this risks false positives
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Gastroschisis: usually right-sided, no peritoneal covering, normal cord insertion; omphalocele: covered, cord at apex
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Beckwith–Wiedemann syndrome – check neonatal blood glucose (hypoglycaemia risk, long-term neurological harm if missed)
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Ruptured omphalocele sac → manage as gastroschisis; associated with ↑mortality
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Delayed atresia repair 4–6 weeks post gastroschisis closure – reduces anastomotic leak risk
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TOP Ground E cut-off 24 weeks; feticide mandatory if performed beyond 21+6 weeks
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MDT = fetal medicine + obstetrics + paediatric surgery + neonatology – anxiety reduction independent of anomaly severity
ANTENATAL FEATURES AT A GLANCE
Omphalocele: membrane-covered, cord at apex, msAFP↑
Gastroschisis: uncovered, right of normal cord, oligohydramnios up to 25%
ABBREVIATION KEY
WHO — World Health Organization CVS — chorionic villus sampling
GI — gastrointestinal PPROM — preterm prelabour rupture of membranes
FASP — fetal anomaly screening programme ELCS — elective caesarean section
msAFP — maternal serum alpha-fetoprotein TOP — termination of pregnancy
CHD — congenital heart defect(s) BMI — body mass index
MDT — multidisciplinary team OEIS — omphalocele, exstrophy of bladder, imperforate anus, spinal defects (complex)
Source: The Obstetrician & Gynaecologist (TOG), RCOG journal — 2023;25:186–195. doi:10.1111/tog.12884
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