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Updated: Sep 15, 2026

Murine Fetal Echocardiography
Published on: February 15, 2013
Arterial Doppler ultrasound in 115 second- and third-trimester fetuses with congenital heart disease
C Meise1, U Germer, U Gembruch
1Division of Prenatal Medicine, Department of Obstetrics and Gynaecology, Medical University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Insights
Isolated congenital heart disease (CHD) does not significantly alter fetal umbilical artery Doppler waveforms for diagnosis. Other factors like extracardiac anomalies often cause changes, limiting Doppler
Area of Science:
- Fetal Medicine
- Cardiology
- Medical Imaging
Background:
- Congenital heart disease (CHD) is a common birth defect.
- Assessing fetal well-being in CHD pregnancies is crucial.
- Doppler ultrasound is used to evaluate fetal circulation.
Purpose of the Study:
- To investigate the impact of isolated congenital heart disease (CHD) on fetal arterial Doppler blood flow velocity waveforms.
- To determine if Doppler findings can aid in diagnosing isolated CHD.
- To differentiate Doppler changes caused by isolated CHD versus other complications.
Main Methods:
- Doppler flow velocimetry of umbilical and middle cerebral arteries was performed in 115 fetuses with antenatally diagnosed CHD.
- Fetuses were categorized into isolated CHD (Group A) and CHD with other complications (Group B).
- A control group of 100 healthy fetuses was used for comparison; pulsatility index (PI) Z-scores were analyzed.
Main Results:
- Fetuses with CHD showed significantly higher umbilical artery PI (delta values) than controls (P < 0.001).
- However, only 7% of isolated CHD cases had elevated umbilical artery PI; most elevations were linked to extracardiac issues.
- No significant differences in middle cerebral artery blood flow were found between groups.
Conclusions:
- Fetal arterial Doppler waveforms in isolated CHD lack sufficient alterations for diagnostic value.
- Elevated umbilical artery PI in CHD is often due to extracardiac anomalies, not the heart defect itself.
- Umbilical artery Doppler is not clinically useful for predicting fetal outcomes in CHD.
Objective:
To assess the influence of isolated congenital heart disease (CHD) on fetal arterial Doppler blood flow velocity waveforms.
Methods:
Doppler flow velocimetry was performed in the umbilical artery and middle cerebral artery in 115 consecutive fetuses with antenatally diagnosed CHD. Gestational age ranged between 19 and 41 weeks. Fetuses with isolated CHD were defined as group A (n = 55), showing cardiogenic hydrops fetalis in six cases; group B included 60 cases complicated by chromosomal or non-chromosomal extracardiac malformation, uteroplacental dysfunction or non-cardiogenic non-immune hydrops fetalis. The control group comprised 100 healthy fetuses of uncomplicated pregnancies. Individual pulsatility index measurements were converted into their Z-scores (delta values) for statistical analysis.
Results:
In regard to the umbilical artery pulsatility index, 115 fetuses with CHD showed a significantly greater (P < 0.001) difference from the normal mean for gestation (delta values) than the control group. However, 29 of the 33 cases with indices above the 95% reference interval were additionally associated with extracardiac malformations, uteroplacental dysfunction or non-cardiogenic non-immune hydrops fetalis. While fetuses with isolated CHD still showed significantly higher values than healthy fetuses (P < 0.01), only in 4 of 55 (7%) fetuses did the measured umbilical artery pulsatility index exceed the 95% reference interval. There was no significant difference from the control group, in which 4 of 100 cases showed an umbilical artery pulsatility index above the 95% reference interval. Elevated umbilical artery pulsatility indices were seen in only four cases of severe obstruction of the outflow tracts leading to reverse perfusion of the affected great artery and in one case of Ebstein's anomaly with pulmonary insufficiency. Although all four fetuses with isolated CHD and elevated umbilical artery pulsatility index died, 14 of 18 fetuses with lethal outcome had normal pulsatility index values in the umbilical artery. Investigations of the middle cerebral artery blood flow revealed no significant difference between fetuses with and without CHD or any subgroups.
Conclusions:
This study shows that arterial blood flow velocity waveforms in fetuses with isolated CHD do not show sufficient alterations to be of diagnostic value. Only in severe outflow tract obstructions due to a 'steal effect' or in significant insufficiencies of semilunar valves leading to an impaired 'wind-kessel function' may the special hemodynamic changes induced by CHD result in a significant increase of pulsatility index in the umbilical artery. In the majority of cases with CHD the increase of pulsatility index of umbilical arterial blood flow velocity waveforms, however, results from extracardiac anomalies, especially uteroplacental dysfunction and chromosomal abnormalities. Furthermore, umbilical artery Doppler sonography is not clinically helpful in predicting fetal outcome.
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