Children with more mild forms of total anomalous pulmonary venous return may only have mild feeding and breathing problems in infancy.
Children with more severe total anomalous pulmonary venous return may have bluish discoloration of the skin (cyanosis), shortness of breath, and fatigue.
Children with the most severe forms of this anomaly may develop severe respiratory distress and cyanosis shortly after birth.
Echocardiography is needed for diagnosis.
Surgical repair is needed.
(See also Overview of Heart Defects.)
Total anomalous pulmonary venous return (TAPVR) accounts for 1 to 2% of birth defects of the heart.
Normally, the pulmonary veins return blood that has picked up oxygen in the lungs to the left atrium. This oxygenated blood then flows from the left atrium into the left ventricle, where it is pumped to the body. (See also Normal Fetal Circulation.) In infants born with total anomalous pulmonary venous return, the pulmonary veins do not connect normally to the left atrium and connect instead by an abnormal pathway eventually leading to the right atrium. So the right atrium, which usually receives only deoxygenated blood from the body to be pumped to the lungs, receives a mix of oxygenated and deoxygenated blood. The additional blood return causes an increased workload and enlargement of the right side of the heart. Even more importantly, blood flow from the pulmonary veins makes its way to the right atrium through various pathways, going up above the heart, down below the heart, or around the back wall of the heart. These pathways can be narrow or blocked, causing blood to back up in the lungs and pressure to build up in the lungs, preventing their normal function. Blood only flows to the left side of the heart through a hole between the right and left atria (a patent foramen ovale or atrial septal defect).
Total Anomalous Pulmonary Venous Return
Newborns with a severe form of TAPVR have difficulty breathing and bluish coloration of the skin (cyanosis).
In milder forms, symptoms of heart failure (see figure Types of Heart Failure) may be present but be more difficult to detect. Symptoms of heart failure include shortness of breath and fatigue. Some infants may have no symptoms.
Diagnosis is suspected based on the findings on a chest x-ray. Diagnosis is confirmed by echocardiography (ultrasonography of the heart). Occasionally, magnetic resonance imaging (MRI) of the heart or computed tomography (CT) angiography may be needed so doctors can more clearly view the defect.
Newborns with TAPVR require surgery early in life. When there is severe obstruction in the pulmonary venous pathway, emergency surgical repair is often needed. Heart failure should be treated with drugs to improve breathing until surgery can be done.
Surgical repair consists of creating a wide open connection between the pulmonary veins and the left atrium. The abnormal connection pathway from the left atrium is tied off.
Some children need to take antibiotics before visits to the dentist and before certain surgeries (such as on the respiratory tract). These antibiotics are used to prevent serious heart infections called endocarditis.
The following are some English-language resources that may be useful. Please note that THE MANUAL is not responsible for the content of these resources.
American Heart Association: Common Heart Defects: Provides an overview of common birth defects of the heart for parents and caregivers
American Heart Association: Infective Endocarditis: Provides an overview of infective endocarditis, including summarizing antibiotic use, for parents and caregivers