MRI characterization of hemodynamic patterns of human fetuses with cyanotic congenital heart disease

L Sun1,2, J F P van Amerom2, D Marini2

  • 1Cardiovascular Center, Children's Hospital of Fudan University, Shanghai, China.

Insights

Fetal congenital heart disease (CHD) significantly alters blood flow and oxygen transport. These changes in fetal circulation may impact prenatal development and the neonatal period for infants with cyanotic CHD.

Area of Science:

  • Cardiovascular Physiology
  • Fetal Medicine
  • Medical Imaging

Background:

  • Congenital heart disease (CHD) encompasses a range of structural abnormalities present at birth.
  • Cyanotic CHD presents unique challenges in fetal circulation and oxygenation.
  • Understanding fetal circulatory dynamics is crucial for predicting neonatal outcomes.

Purpose of the Study:

  • To characterize blood flow and oxygen transport in fetuses with cyanotic congenital heart disease using magnetic resonance imaging (MRI).
  • To identify specific patterns of circulatory alterations in various subtypes of fetal CHD.

Main Methods:

  • Cine phase-contrast MRI was employed to measure blood flow in major fetal vessels.
  • Oxygen saturation (SaO2) was assessed in key vessels of fetuses with CHD and controls.
  • The study included 152 fetuses with CHD and 40 gestational-age-matched controls.

Main Results:

  • Fetuses with single-ventricle physiology showed reduced combined ventricular output.
  • Obstructive lesions were linked to altered flow on the contralateral side.
  • Reduced pulmonary and umbilical blood flow were observed in specific CHD subtypes like Ebstein's anomaly.
  • Lower oxygen saturation was noted in the ascending aorta and superior vena cava across most CHD subtypes.

Conclusions:

  • Cyanotic CHD leads to significant alterations in fetal blood flow and oxygen transport.
  • These circulatory changes affect cerebral, pulmonary, and placental oxygenation.
  • The identified physiological changes may explain prenatal growth abnormalities and influence the neonatal course in affected infants.
Abstract

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