Fetal cardiac dimensions in congenital diaphragmatic hernia: relationship with gestational age and postnatal outcomes

Anna Claudia Massolo1, Anita Romiti2, Milena Viggiano2

  • 1Department of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy. annaclaudia.massolo@opbg.net.

Insights

Fetal cardiac measurements, including mitral valve diameter (MVD), are reduced in congenital diaphragmatic hernia (CDH). Smaller MVDs in early gestation may predict severe CDH outcomes.

Area of Science:

  • Fetal cardiology
  • Congenital abnormalities
  • Neonatal outcomes

Background:

  • Congenital diaphragmatic hernia (CDH) is a serious condition affecting fetal development.
  • Cardiac anomalies are frequently observed in fetuses with CDH.
  • Understanding fetal cardiac changes is crucial for predicting CDH severity.

Purpose of the Study:

  • To serially assess fetal cardiac dimensions in congenital diaphragmatic hernia (CDH).
  • To determine the relationship between fetal cardiac dimensions and CDH disease severity.

Main Methods:

  • Retrospective analysis of CDH cases and matched controls.
  • Serial assessment of mitral valve diameter (MVd), tricuspid valve diameter (TVd), left ventricular (LV) length and area, and their Z-scores.
  • Measurements taken at 24-26, 30-32, and 35-37 weeks gestational age (GA).

Main Results:

  • CDH cases showed significantly reduced MVd, MVd Z-score, and LV area at 24-26 and 35-37 weeks GA.
  • Reduced TVd, TVd Z-score, and RV area were observed at 24-26 weeks GA in CDH.
  • Lower MVd and MVd Z-scores at 24-26 weeks GA were associated with combined outcomes of death and/or extracorporeal membrane oxygenation (ECMO).

Conclusions:

  • Left ventricular (LV) hypoplasia in CDH is indicated by reduced MVd from 24 weeks GA.
  • MVd and the ratio of mitral to tricuspid valve diameters may predict CDH disease severity.
Abstract