Progression of congenital heart disease in the prenatal period
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Published on: May 5, 2018
1Department of Pediatrics, Kurume University School of Medicine, Japan. yasukim@med.kurume-u.ac.jp
Insights
Congenital heart disease can develop before birth, with changes in fetal heart structure and function impacting diagnosis. Understanding prenatal progression is key for accurate diagnosis, management, and improved outcomes for affected infants.
Area of Science:
- Cardiology
- Fetal Medicine
- Pediatric Cardiology
Background:
- Prenatal echocardiography reveals congenital heart disease development during gestation.
- Fetal cardiac anatomy and function evolve, altering postnatal appearance of cardiac anomalies.
Purpose of the Study:
- To review and discuss the in utero development of congenital heart disease from mid-gestation to the early postnatal period.
- To highlight the importance of understanding prenatal progression for diagnosis and management.
Main Methods:
- Systematic review of published prenatal echocardiographic studies.
- Discussion of in utero development of congenital heart disease.
Main Results:
- Ventricular outflow obstruction reduces great vessel and ventricle growth; valve regurgitation may worsen.
- Restrictive foramen ovale and ductus arteriosus, progressive pulmonary vascular obstructive changes, and fetal arrhythmias can occur in utero.
- Congestive heart failure, fetal hydrops, and poor prognosis are significant concerns in affected fetuses.
Conclusions:
- Accurate prenatal diagnosis and management planning require knowledge of congenital heart disease progression.
- Predicting in utero progression is crucial for counseling families and assessing prenatal vs. postnatal treatment benefits.
- Further extensive studies are needed to accurately predict progression and elucidate underlying mechanisms for better fetal outcomes.
Background:
Prenatal echocardiography has shown evidence of prenatal development of congenital heart disease. Prenatal cardiac anatomy, chamber size and function change during gestation, so that the appearance of cardiac structure in abnormal hearts may be different from that which is usually seen postnatally.
Methods:
Published prenatal echocardiographic studies were reviewed and in utero development of congenital heart disease from midtrimester to the early postnatal period is discussed.
Results:
The growth of the great vessels and ventricles is reduced in fetuses with ventricular outflow obstruction. Valve regurgitation may progress. The foramen ovale and ductus arteriosus have been reported to become restrictive in utero in several settings. Pulmonary vascular obstructive changes may progress prenatally. Fetal arrhythmia (both bradycardia and tachycardia) may develop in utero. Development of congestive heart failure is a very important issue during follow up of fetuses with significant cardiac or extracardiac problems. Some may progress to fetal hydrops and prognosis of the affected fetuses is usually very poor.
Conclusions:
Correct knowledge of possible development is important for accurate prenatal diagnosis. Information on prenatal progression of the cardiac anomaly is also important to make plans for follow up and perinatal management, to predict outcomes and to counsel family. Furthermore, the benefits of prenatal treatment instead of postnatal treatment should be assessed by the accurate prediction of the progression of the cardiac problem in utero. Further extensive studies using a large number of cases is required to predict progression accurately. In addition, further studies for elucidating the mechanisms of progression is important to provide better outcomes for fetuses with various congenital heart diseases.
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