Outcomes following antenatal identification of hydrops fetalis: a single-centre experience from 2001 to 2012. Issue 3 (16th May 2018)

• Record Type: Journal Article
• Authors: Gilby, Damien M; Mee, J Bridie; Kamlin, C Omar Farouk; Kornman, Louise H; Davis, Peter G; Manley, Brett James
• Is Part Of: Archives of disease in childhood. Volume 104:Issue 3(2019)
• Page Start: F253
• Page End: F258
• Publication Date: 2018-05-16
• Subjects: hydrops fetalis -- fetus -- newborn -- congenital anomaly; Infants -- Diseases -- Periodicals; Newborn infants -- Diseases -- Periodicals; Fetus -- Diseases -- Periodicals; 618.920105
• DOI: 10.1136/archdischild-2017-313604
• Languages: English
• ISSNs: 1359-2998

Abstract

Abstract : Objective: To describe the aetiologies and outcomes of pregnancies complicated by hydrops fetalis (HF). Study design: Case series of all pregnancies complicated by HF managed at The Royal Women's Hospital (RWH), Melbourne, Australia, between 2001 and 2012. Multiple pregnancies, and cases where antenatal care was not provided at RWH were excluded. Cases were identified from neonatal and obstetric databases. Data were extracted from maternal and neonatal case files, electronic pathology and radiology reports, and obstetric and neonatal databases. Results: Over 12 years, 131 fetuses with HF with a median (IQR) gestational age (GA) at diagnosis of 24 (20–30) weeks were included in the analysis. There were 65 liveborn infants with a median (IQR) GA at birth of 33 (31–37) weeks and a median (IQR) birthweight Z-score of 1.4 (0.4–2.2). Overall survival from diagnosis was 27% (36/131) increasing to 55% (36/65) if born alive. Conclusions: The perinatal mortality risk for fetuses and newborn infants with HF is high with important differences dependent on underlying diagnosis and the time at which counselling is provided. Clinicians need to be aware of the outcomes of both fetuses and neonates with this condition.