Fetus
Poster Session 2
Fiona Cody, MSc PhD scholar (she/her/hers)
Clinical specialist sonographer in Obstetric ultrasound/PhD scholar
Royal College of Surgeons in Ireland
Dublin, Ireland, Ireland
Orla Franklin, FRCOG, MBA
CHI at Crumlin Children's Hospital, Trinity College Dublin
Dublin, Ireland, Ireland
Nicola Mc Cay, MD
Specialist pediatric cardiology registrar
CHI at Crumlin Children's Hospital
Dublin, Ireland, Ireland
Zara Molphy, PhD
Royal College of Surgeons in Ireland
Dublin, Ireland, Ireland
Patrick Dicker, MA, MSc, PhD
Biostatistician
Royal College of Surgeons in Ireland
Dublin, Ireland, Ireland
Fionnuala M. Breathnach, FRCOG, MD, MSc
Obstetrician & Gynecologist
Royal College of Surgeons in Ireland
Dublin, Ireland, Ireland
A 4-year retrospective cohort study examined all cases of CCHD requiring intervention in the first 4 weeks of life among infants delivered in a perinatology center and its affiliated regional sites. All cases of CCHD that underwent pregnancy termination, died in-utero or in the early neonatal period were also ascertained. The protocolised prenatal screening service included a scan at 18-22 weeks, repeat screening for cases of non-acquisition of defined 4-chamber or outflow tract views and Fetal Medicine review in the event of non-acquisition on 2nd attempt. CCHD was defined as duct-dependency or cardiac abnormality requiring urgent intervention in the first 4 weeks of life. All cases were referred to a single national pediatric cardiac centre. Data sources included dedicated prenatal ultrasound and pediatric cardiology databases, perinatal, neonatal and pediatric chart review.
Results:
From 01/2019 to 12/2022, among a consecutive cohort of 49,950 pregnancies who underwent prenatal screening for congenital heart disease, 104 cases (0.2%) were significant for CCHD, of whom 91% (95/104) were detected in the prenatal period. Aortic coarctation represented 78% (7/9) of CCHD cases first identified in the neonatal period, with 2 additional cases of postnatally-identified pulmonary stenosis. No case of single-ventricle pathology nor of transposition of the great arteries was missed by the prenatal screening program.
Conclusion:
Prenatal detection of CCHD in a tertiary care unit and its affiliated sites exceeds 91%, with undetected cases limited to outflow tract obstructive lesions that may not be amenable to prenatal detection.