Cardiac fetal ultrasonographic parameters for predicting outcomes of isolated left-sided congenital diaphragmatic

Masaya Yamoto1, Yasuhiko Tanaka2, Koji Fukumoto1

  • 1Department of Pediatric Surgery, Shizuoka Children's Hospital, Shizuoka, Japan.

Journal of Pediatric Surgery
|September 29, 2015
PubMed

Insights

Fetal cardiac ultrasound measurements can predict outcomes for isolated left-sided congenital diaphragmatic hernia (CDH). The tricuspid valve to mitral valve (TV/MV) ratio is a reliable indicator for survival in CDH patients.

Area of Science:

  • Perinatology
  • Fetal Cardiology
  • Congenital Anomalies

Background:

  • Isolated left-sided congenital diaphragmatic hernia (CDH) presents significant challenges in predicting fetal outcomes.
  • Fetal cardiac ultrasonography offers potential for non-invasive assessment of cardiac function and structure.

Purpose of the Study:

  • To investigate fetal cardiac ultrasonographic parameters in relation to outcomes of isolated left-sided CDH.
  • To identify specific echocardiographic markers that correlate with survival in fetuses diagnosed with CDH.

Main Methods:

  • Comparison of cardiothoracic area ratio (CTAR), main pulmonary artery to ascending aorta diameter ratio (MPA/AAo), and tricuspid valve to mitral valve diameter ratio (TV/MV) between CDH fetuses and controls.
  • Analysis of these parameters in relation to survival (SG) and non-survival (NSG) groups within the CDH cohort.

Main Results:

  • All three ultrasonographic parameters (CTAR, MPA/AAo, TV/MV) differed significantly between CDH fetuses and controls.
  • CTAR and TV/MV ratios showed significant differences between survival and non-survival groups.
  • A TV/MV ratio >1.72 effectively discriminated between survivors and non-survivors, with increasing TV/MV ratio correlating with gestational age.

Conclusions:

  • Fetal cardiac ultrasonography is a valuable tool for predicting outcomes in isolated left-sided CDH.
  • The TV/MV ratio emerges as a reliable indicator for assessing the prognosis of fetuses with isolated left-sided CDH.
Abstract

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