Poster Session 4
Category: Ultrasound/Imaging
Poster Session 4
Alex Dakin, MBBCH
Department of Obstetrics and Gynaecology, Royal College of Surgeons in Ireland
Dublin, Dublin, Ireland
Ronan Daly, MBBS
Royal College of Surgeons Ireland - Rotunda Hospital
Dublin, Dublin, Ireland
Denisa Asandei, MSc
Department of Obstetrics and Gynaecology, Royal College of Surgeons in Ireland
Royal College of Surgeons in Ireland, Dublin, Ireland
Zara Molphy, PhD
Royal College of Surgeons in Ireland
Dublin, Dublin, Ireland
Patrick Dicker, BA, MA, MSc, PhD (he/him/his)
Biostatistician
Department of Obstetrics and Gynaecology, Royal College of Surgeons in Ireland, Dublin, Ireland.
Royal College of Surgeons in Ireland, Dublin, Ireland
Michael Boyle, MBBS, PhD
Rotunda Hospital
Rotunda Hospital, Dublin, Ireland
Etaoin Kent, FRCOG, MBBCH
Consultant Fetal Maternal Medicine Specialist
Rotunda Hospital
Dublin, Dublin, Ireland
Fergal D. Malone, FRCOG, MD
Professor and Chairman of the Department of Obstetrics and Gynaecology at the Royal College of Surge
Royal College of Surgeons in Ireland
Dublin, Dublin, Ireland
Early-onset fetal growth restriction (EOFGR) is associated with significant perinatal morbidity and mortality. Our aim was to determine perinatal and infant outcomes of EOFGR, and to evaluate for presence of antenatal predictors of these adverse outcomes.
Study Design:
A retrospective cohort study was carried out from July 2016 to June 2022 of singleton pregnancies with uteroplacental EOFGR diagnosed prior to 32 weeks’ gestation, per Delphi consensus definition, at a tertiary institution with over 8,000 deliveries per year. Genetic, structural or infectious causes were excluded, along with preterm pre-labour rupture of membranes. Adverse outcome was defined as either perinatal mortality (intrauterine fetal demise or neonatal death) or composite neonatal morbidity (outlined in figure 1).
Results:
622 cases of EOFGR were diagnosed during the study period, of which 55% (341/622) were uteroplacental in origin. There was a 95% livebirth rate (325/341), and no terminations of pregnancy. There were 16 intrauterine fetal deaths (7.8%, 16/341) and 11 neonatal deaths (3.2%, 11/341), all occurring in cases diagnosed prior to 28 weeks’ gestation. Adverse outcomes of this cohort are described in figure 1. Table 1 correlates presence or absence of adverse outcome with maternal demographics, ultrasound characteristics and pregnancy outcomes. Unsurprisingly, earlier gestation and lower birthweight at delivery were associated with worse perinatal outcome, along with earlier gestation at diagnosis.
Conclusion:
Reassuringly, there was a high livebirth rate in our cohort, however almost one in four pregnancies experienced an adverse outcome. Maternal demographics such as obesity, assisted reproductive technology, and chronic hypertension are not only risk factors for development of EOFGR, but also markers of its severity. Doppler abnormalities on the last ultrasound prior to delivery are more predictive of adverse outcome than amniotic fluid abnormalities, and development of co-existent pre-eclampsia confers higher risk. This information provides valuable insights for clinicians caring for these high-risk pregnancies.