Fetal single ventricle journey to first postnatal procedure: a multicentre UK cohort study

Arch Dis Child Fetal Neonatal Ed. 2024 Jun 19;109(4):384-390. doi: 10.1136/archdischild-2023-326213.

Abstract

Objectives: UK single ventricle (SV) palliation outcomes after first postnatal procedure (FPP) are well documented. However, survival determinants from fetal diagnosis to FPP are lacking. To better inform parental-fetal counselling, we examined factors favouring survival at two large UK centres.

Design: Retrospective multicentre cohort study.

Setting: Two UK congenital cardiac centres: Leeds and Birmingham.

Patients: SV fetal diagnoses from 2015 to 2021.

Main outcome measures: Survival from fetal diagnosis with intention to treat (ITT) to birth and then FPP. Maternal, fetal and neonatal risk factors were assessed.

Results: There were 666 fetal SV diagnoses with 414 (62%) ITT. Of ITT, 381 (92%) were live births and 337 (81%) underwent FPP. Survival (ITT) to FPP was notably reduced for severe Ebstein's 14/22 (63.6%), unbalanced atrioventricular septal defect 32/45 (71%), indeterminate SV 3/4 (75%), mitral atresia 8/10 (80%) and hypoplastic left heart syndrome 127/156 (81.4%). Biventricular pathway was undertaken in five (1%). After multivariable adjustment, prenatal risk factors for mortality were increasing maternal age (OR 1.05, 95% CI 1.0 to 1.1), non-white ethnicity (OR 2.6, 95% CI 1.4 to 4.8), extracardiac anomaly (OR 6.34, 95% CI 1.8 to 22.7) and hydrops (OR 7.39, 95% CI 1.2 to 45.1). Postnatally, prematurity was significantly associated with mortality (OR 6.3, 95% CI 2.3 to 16.8).

Conclusions: Around 20% of ITT fetuses diagnosed with SV will not reach FPP. Risk varies according to the cardiac lesion and is significantly influenced by the presence of an extracardiac anomaly, fetal hydrops, ethnicity, increasing maternal age and gestation at birth. These data highlight the need for fetal preprocedure data to be used in conjunction with procedural outcomes for fetal counselling.

Keywords: Cardiology; Mortality; Neonatology; Paediatrics.

Publication types

  • Multicenter Study

MeSH terms

  • Female
  • Heart Defects, Congenital* / mortality
  • Heart Defects, Congenital* / surgery
  • Heart Ventricles* / abnormalities
  • Humans
  • Infant, Newborn
  • Male
  • Palliative Care
  • Pregnancy
  • Prenatal Diagnosis
  • Retrospective Studies
  • Risk Factors
  • United Kingdom / epidemiology