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Cardiac Findings in Fetal and Pediatric Autopsies: A 15-Year Retrospective Review
Mana Taweevisit1, Paul Thorner1,2
1a Pathology, Faculty of Medicine , Chulalongkorn University , Bangkok , Thailand.
Insights
Autopsies reveal a wide spectrum of congenital heart defects (CHDs) in pediatric patients. Postmortem examination is crucial for accurate diagnosis and genetic counseling.
Area of Science:
- Pediatric Pathology
- Cardiovascular Research
- Medical Genetics
Background:
- Congenital heart defects (CHDs) are a leading cause of morbidity and mortality in children.
- Understanding the spectrum of CHDs is vital for improving patient outcomes.
- Autopsy remains a critical tool for diagnosing CHDs and associated anomalies.
Purpose of the Study:
- To determine the spectrum of congenital heart defects (CHDs) using fetal and pediatric autopsies.
- To correlate autopsy findings with prenatal echocardiography.
- To assess the diagnostic accuracy of prenatal imaging for CHDs.
Main Methods:
- Retrospective review of 608 autopsy reports over 15 years.
- Correlation of postmortem findings with echocardiography records.
- Analysis of extracardiac malformations and chromosomal abnormalities in CHD cases.
Main Results:
- 119 cases (19.6%) had congenital heart defects (CHDs).
- Persistent left superior vena cava was the most common defect; 41% had extracardiac malformations, and 18.5% had chromosomal abnormalities.
- Prenatal echocardiography showed 85% correlation with autopsy findings, missing milder defects.
Conclusions:
- Postmortem examination is essential for precise CHD anatomy delineation.
- Autopsies aid in identifying extracardiac malformations and potential genetic syndromes.
- Findings support accurate parental counseling and evaluation of prenatal imaging accuracy.
Introduction:
Congenital heart defects (CHDs) carry significant morbidity and mortality in pediatric patients. This study determined the spectrum of CHDs based on fetal and pediatric autopsies.
Methods:
Autopsy reports over a 15-year period were reviewed. Postmortem findings were correlated with echocardiography records.
Results:
From 608 autopsies, 119 cases with CHDs were identified (11% of fetal, 53% of neonatal, 18% of infant, and 4.5% of childhood autopsies). Persistent left superior vena cava was the most common individual defect. 41% of cases had extracardiac malformations. 18.5% of cases had chromosomal abnormalities. Prenatal echocardiography was available in 52 cases, showing 85% correlation with autopsy findings. Defects missed by echocardiography were generally of mild severity.
Conclusion:
Postmortem examination is important to delineate the anatomy of CHDs, and recognize extracardiac malformations for identification of possible genetic syndromes. This information can be used for parental counseling and for assessment of accuracy of pre-mortem imaging studies.
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