Due to the complexity of HLHS, it is a challenging disease to care for. But our competent doctors at the Children's Hospital Services Lines at The Aga Khan University Hospital are internationally trained so they can provide exemplary medical care to your baby. Their commitment to providing quality healthcare makes them the best in the country.
HLHS is treated with step by step surgical procedures or a heart transplant. After consultation from you, your child may be admitted in the hospital. Initially, the doctor may recommend various options to stabilize their condition. These may include:
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Medications to help dilate blood vessels and keep the ductus arteriosis open
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Breathing assistance with a ventilator
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Intravenous (IV) fluids
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Feeding tube
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Atrial septostomy in which the opening between the two atria is enlarged to promote more blood flow if the foramen ovale closes
The surgical steps include:
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Norwood procedure which is usually performed in the first week of your baby’s life. In this procedure the doctor reconstructs the aorta and connects it to the heart’s left ventricle. A tube is inserted to make a path between the aorta and the pulmonary arteries (arteries leading to the lungs), or they place a tube to connect the right ventricle to the pulmonary arteries. At times, the doctor may perform a hybrid procedure where they implant a stent in the ductus arteriosis to keep it open, place bands around the pulmonary arteries to reduce blood flow to the lungs and create an opening between the two atria
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Bi-directional Glenn procedure which is performed once your child is between three to six months. The doctor removes the shunt on the pulmonary artery and connects the superior vena cava (large veins that returns blood to the heart from the top half of the body) to the pulmonary artery. The blood travels from the top half of body directly to the lungs, for oxygenation, via the pulmonary artery
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Fontan procedure which is performed once your child is between eighteen months and four years. The doctor creates a path for the oxygen-poor blood to travel from the inferior vena cava (veins that carries blood from the rest of the body) to the pulmonary artery and then to the lungs. After this procedure, the oxygen-rich and oxygen-poor blood do not mix
Heart transplant is another option, especially if the defects are very complex. Your child will be kept on medications until a donor heart becomes available.