Strategies For Treating Tricuspid Atresia
Tricuspid atresia is a form of congenital heart disease where the heart has an abnormally developed or missing tricuspid valve. In healthy individuals, blood flows into the heart's right atrium through the tricuspid valve, into the right ventricle, then from the right ventricle to the lungs for oxygen, and then into the left atrium. The oxygenated blood then flows into the left ventricle where it is pumped out of the heart and around the body. However, blood in tricuspid atresia patients flows into the right atrium and through a hole into the left atrium rather than through the tricuspid valve. Affected individuals receive some oxygenated blood through a hole between the right and left ventricles or via a ductus arteriosus connecting the pulmonary artery to the aorta. The oxygen-poor blood that never reaches the lungs mixes with oxygenated blood before being pumped throughout the body.
Treatment for tricuspid atresia involves a series of corrective surgical procedures. Learn more about this now.
Implant A Shunt

It may be necessary for a surgeon to implant a shunt or a bypass from the right subclavian artery or the first artery that branches off of the aorta to the pulmonary artery in infants with tricuspid atresia. This procedure is performed when the infant's oxygen levels urgently need to be brought up. A shunting procedure improves the infant's blood flow from the heart to the lungs. Once the shunt is in place, some of the blood that flows through the infant's aorta towards the rest of the body can pass through this new connection into the pulmonary artery. Once in the pulmonary artery, the blood will pick up oxygen from the lungs and then it returns to the heart. While this new mechanism helps the overall oxygen level circumstances, it does not stop some of the oxygen-poor blood from moving out of the right atrium and into the left atrium and combining with the oxygen-rich blood. This bypass is usually implanted during the first couple weeks of the baby's life. This shunt allows the infant to remain relatively stable for several months, but eventually, the infant will outgrow the shunt and require another surgical procedure to continue treatment.
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Glenn Operation

The Glenn operation is usually the second procedure performed on an infant affected by tricuspid atresia. The procedure may be performed on the patient when they are anywhere between four and twelve months old. This procedure replaces the first shunt with a different and more effective connection arrangement. During the Glenn procedure, the old shunt is removed, and the large vein that carries oxygen-poor blood from the arms and head to the heart or the superior vena cava is attached to the right pulmonary artery. This connection allows blood to flow from the arms and the head directly into the lungs to pick up oxygen. While this new connection arrangement further improves the infant's overall oxygen level, there is still oxygen-poor blood flowing from the lower body into the left chambers in the heart containing oxygen-rich blood. This mechanism means less oxygen-poor blood is mixing with oxygenated blood overall, but it does not entirely resolve the infant's tricuspid atresia. This procedure does, however, make some of the new connections needed to carry out the final surgical procedure that stops all oxygen-poor and oxygen-rich mixing.
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