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Fetal diagnosis of hypoplastic left heart, associations and outcomes in the current era
R Axt-Fliedner1, C Enzensberger1, N Fass1
1Division of Prenatal Medicine, Department of OB/GYN, Justus-Liebig-University, Giessen.
Insights
Prenatal diagnosis of Hypoplastic Left Heart (HLH) allows for informed decisions. Overall survival after fetal diagnosis is 40.9%, with higher rates for surgical candidates.
Area of Science:
- Fetal Cardiology
- Pediatric Cardiac Surgery
- Prenatal Diagnosis
Background:
- Hypoplastic Left Heart (HLH) is a common congenital heart defect diagnosed prenatally.
- Antenatal diagnosis of HLH is crucial for parental counseling and treatment planning.
Purpose of the Study:
- To report outcome data for Hypoplastic Left Heart (HLH) following fetal diagnosis.
- To assess survival rates and factors influencing outcomes in HLH cases diagnosed antenatally.
Main Methods:
- Retrospective analysis of 105 HLH cases diagnosed prenatally between 1994 and 2011.
- Inclusion of data from two tertiary referral centers specializing in prenatal diagnosis and pediatric cardiology.
Main Results:
- Overall survival after prenatal diagnosis was 40.9% (43/105).
- Survival rates were 81.1% for infants undergoing surgery and 64.1% from an intention-to-treat perspective.
- Associated extracardiac or karyotype anomalies were present in 18.9% of cases, often leading to compassionate care decisions or termination of pregnancy.
Conclusions:
- Antenatal evaluation for HLH should include karyotyping and detailed anomaly assessment to predict surgical risks.
- Exclusion of additional anomalies can refine prenatal counseling.
- These findings provide current data to support parental counseling for HLH.
Purpose:
Hypoplastic left heart (HLH) is one of the most common forms of cardiac abnormality detectable during gestation by fetal echocardiography. Antenatal diagnosis allows for appropriate counseling and time to consider treatment options. We report the actual outcome data after fetal diagnosis of HLH.
Materials And Methods:
Retrospective analysis of the outcome in all cases with HLH from 1994 - 2011 presenting in fetal life at two tertiary referral centers for prenatal diagnosis and pediatric cardiology.
Results:
105 cases were included and the overall survival is 40.9 % (43/105) after prenatal diagnosis. There was an 81.1 % survival rate in infants undergoing surgery and a 64.1 % survival rate from an intention-to-treat position. Two neonates died due to tamponade and cardiac arrest following balloon septostomy and one neonate from sepsis before surgery. Extracardiac anomalies occurred in three fetuses, and karyotype anomalies in seven fetuses (18.9 %). In 4 of 5 babies born with additional extracradiac or karyotype anomalies, parents opted for compassionate care. The first had trisomy 13, the second had trisomy 18, the third neonate presented with spina bifida, and the fourth presented with hydronephrosis and pulmonary atresia. Termination of pregnancy took place in 17 cases (16.1 %).
Conclusion:
Thorough antenatal evaluation should include karyotyping, detailed extracardiac and intracardiac assessment to accurately predict the risks of surgery. Prenatal counseling might be modified after the exclusion of additional anomalies. These data provide up-to-date information for parental counseling.
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