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Health Information For Parents
Tricuspid atresia is a congenital heart defect (this means that a baby who has it is born with it). It happens when the heart‘s tricuspid valve does not develop. This means that blood can’t flow from the heart’s right atrium (upper receiving chamber) to the right ventricle (lower pumping chamber) as it should.
A baby born with tricuspid atresia often has serious symptoms soon after birth because blood flow to the lungs is much less than normal.
In a normal heart, the tricuspid valve lets blood flow from the right atrium into the right ventricle. When the right ventricle squeezes to pump blood to the lungs, the tricuspid valve closes. This keeps blood from flowing back into the right atrium.
The right side of the heart (the right atrium and the right ventricle) gets oxygen-poor blood from the body and pumps it to the lungs. Then, the lungs add fresh oxygen to the blood. The blood, now full of oxygen, returns to the left side of the heart. The left atrium gets the oxygen-rich blood and passes it to the left ventricle, which then pumps it out to the body.
In a heart with tricuspid atresia, solid tissue sits between the right atrium and the right ventricle. Because blood in the right atrium can’t move through the tricuspid valve, the wall separating the right and left sides of the heart does not form completely.
In most babies with tricuspid atresia, the heart has two holes:
Oxygen-poor blood received by the right atrium can only flow by the atrial septal defect (ASD). The oxygen-poor blood passes through the ASD into the left atrium, where it mixes with oxygen-rich blood. The left atrium passes the mixed blood to the left ventricle. The left ventricle pumps most of the mixed blood to the body, but some pushes through the ventricular septal defect (VSD) and the right ventricle to the lungs.
Soon after birth, a newborn with tricuspid atresia usually will:
Tricuspid atresia happens when the heart forms very early in pregnancy. No one knows why the the valve doesn’t grow normally.
A baby is more likely to have tricuspid atresia if:
But, having one or more risk factors doesn’t mean that a baby will have tricuspid atresia. Tricuspid atresia can happen without any risk factors.
Tricuspid atresia sometimes is seen on ultrasound scans before birth. A fetal echocardiogram (a more detailed ultrasound study of the unborn baby’s heart) can give more information and help the delivery team plan treatment.
A screening pulse oximeter test usually is done on all newborns right after birth using a light on a fingertip or toe. If tricuspid atresia isn’t found before birth, this test will show that the baby’s blood is not carrying as much oxygen as expected. The delivery team will then do other tests to find the problem and help plan treatment.
The tests may include:
Treatment for tricuspid atresia combines medicine, surgery, and cardiac catheterization to improve the flow of blood to the lungs. Replacing the tricuspid valve does not help because the right ventricle is not large enough to pump blood well.
A medicine called prostaglandin E1 helps keep the ductus arteriosus (often just called “the ductus”) open. The ductus arteriosus is a normal blood vessel that connects two major arteries — the aorta and the pulmonary artery — that carry blood away from the heart. Keeping the ductus open in babies with tricuspid atresia improves the flow of blood to the lungs.
These surgical steps (called the single ventricle pathway) can improve blood flow to the lungs in a baby with tricuspid atresia:
Doctors decide which steps to take based on what they learn from all the tests.
Cardiac catheterization can make or enlarge openings in the wall between the two atria and between the two ventricles. It also can be used to place a stent (mesh tube) in the ductus to keep it open.
Treatments for tricuspid atresia improve the baby’s condition, but can’t make the heart work like one without a defect. A child born with tricuspid atresia will regularly see a cardiologist (a doctor who treats heart problems) throughout childhood and as an adult.
The heart and circulatory system are our body’s lifeline, delivering blood to the body’s tissues. Brush up on your ticker with this body basics article.
Hypoplastic left heart syndrome (HLHS) is a birth defect of a babyâs heart. The left side of the heart doesnât grow as it should, making it smaller and weaker than normal.
This minimally invasive procedure helps doctors performÂ diagnostic tests on the heart and even treat some heart conditions.
Atrial septal defect (ASD) â also known as a “hole in the heart” â is a type of congenital heart defect. Most ASDs are diagnosed and treated successfully.
Double outlet right ventricle (DORV) is a heart defect where the aorta connects to the heart in the wrong place.
Heart defects happen when there’s a problem with a baby’s heart development during pregnancy. Most heart defects can be treated during infancy.
An interrupted aortic arch (IAA) is a rare heart condition in which the aorta doesnât form completely. Surgery must be done within the first few days of a babyâs life to close the gap in the aorta.
Truncus arteriosus is a heart defect that happens when a child is born with one large artery instead of two separate arteries.
Ventricular septal defect (VSD) â also known as a “hole in the heart” â is a congenital heart defect. Most VSDs are diagnosed and treated successfully.
A guide to medical terms about the heart and circulatory system. In an easy A-Z format, find definitions on heart defects, heart conditions, treatments, and more.
Usually, a heart has two working ventricles (pumping chambers). Having a single ventricle means that only one of the two ventricles works well enough to pump blood.
Note: All information is for educational purposes only. For specific medical advice, diagnoses, and treatment, consult your doctor.
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