All infants with complete transposition of the great arteries (
D-TGA) need surgery to correct the heart problem. Treatment for congenitally corrected transposition (
L-TGA) depends on when the condition is diagnosed and what other heart conditions exist.
Medications
Before surgery is done to fix the switched arteries, a medicine called alprostadil (Caverject, Edex, others) may be given to the baby. This medicine increases blood flow. It helps oxygen-poor and oxygen-rich blood better mix together.
Surgery or other procedures
Surgery for transposition of the great arteries (TGA) is usually done within the first days to weeks after birth. Options depend on the type of
TGA. Not all people with congenitally corrected transposition need surgery.
Surgeries and other treatments used to treat transposition of the great arteries may include:
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Atrial septostomy. This treatment may be done urgently as a temporary fix before surgery. It uses thin tubes and small cuts to widen a natural connection between the heart's upper chambers. It helps mix oxygen-rich and oxygen-poor blood, improving oxygen levels in the baby's body.
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Arterial switch operation. This is the most common surgery used to correct transposition of the great arteries. During this surgery, the two main arteries leaving the heart are moved to their correct positions. Other heart problems present at birth may be repaired during this surgery.
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Atrial switch operation. The surgeon splits blood flow between the heart's two upper chambers. After this surgery, the right lower heart chamber must pump blood to the body, instead of just to the lungs.
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Rastelli procedure.
This surgery may be done if a baby with
TGA also has a hole in the heart called a ventricular septal defect. The surgeon patches the hole and redirects blood flow from the left lower heart chamber to the aorta. This lets oxygen-rich blood go to the body. An artificial valve connects the right lower heart chamber to the lung artery.
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Double switch procedure. This complex surgery is used to treat congenitally corrected transposition. It redirects blood flow coming into the heart. It switches the great artery connections so the left lower heart chamber can pump oxygen-rich blood to the aorta.
Babies born with
TGA
often have other heart problems. Other surgeries may be needed to fix those heart problems. Surgery also may be needed to treat complications of
TGA. If
TGA causes changes in the heartbeat, a device called a pacemaker may be recommended.
After surgery to fix
TGA, lifelong care is needed with a provider trained in heart problems present at birth. This type of health care provider is called a congenital cardiologist.