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Hypoplastic Left Heart Syndrome


What Is Hypoplastic Left Heart Syndrome?

Hypoplastic left heart syndrome (HLHS) is a heart defect in which the left side of the heart does not grow to its usual size and strength.

Babies who have HLHS are born with it.

What Happens in Hypoplastic Left Heart Syndrome?

After birth, the job of the right side of the heart is to pump blood to the lungs. The job of the left side of the heart is to pump blood to the rest of the body. Pumping blood to the body is harder work than pumping blood to the lungs, so the left ventricle is usually stronger than the right ventricle.

To do both jobs properly, a newborn's body normally closes two openings in the heart:

  1. the ductus arteriosus, a connection between two large blood vessels closes during the first days after birth
  2. the foramen ovale, an opening between the left atrium and right atrium (the blood-receiving chambers of the heart) closes during the first few weeks of life

In a baby with HLHS, the left side of the heart can't do its job. When one or both of the openings close, the right side of the heart can't help the left side, so the symptoms get worse.

What Problems Can Happen?

A newborn with HLHS may not look sick right away. But problems are already present and can include:

What Are the Signs & Symptoms of Hypoplastic Left Heart Syndrome?

Starting a few hours to a day or so after delivery, a newborn with untreated HLHS will have:

Without treatment, the baby's blood pressure will fall too low to meet the body's needs, a condition called "shock."

What Causes Hypoplastic Left Heart Syndrome?

Most cases of HLHS happen in the developing heart during early pregnancy. Some might be due to a combination of genes and things in the baby's and mother's environment during this early stage.

Who Gets Hypoplastic Left Heart Syndrome?

There is a very small chance of HLHS in every pregnancy and a higher chance in a second pregnancy if the first baby had HLHS. Babies with certain genetic problems (syndromes) have a greater chance of having HLHS, but no single gene has been found to cause it.

How Is Hypoplastic Left Heart Syndrome Diagnosed?

HLHS may be seen on fetal (before birth) ultrasound scans. A fetal echocardiogram (a detailed ultrasound scan of the fetal heart) provides more information and tells the delivery team how to prepare for care after birth.

Common tests used to learn more about a newborn's heart include:

How Is Hypoplastic Left Heart Syndrome Treated?

Treatment is essential for a newborn with HLHS. The treatment plan includes:

Ventilator Support

A ventilator sometimes is used to help the baby breathe and let the intensive care team adjust oxygen levels, which can help keep blood flow to the body and lungs in balance.

Surgery

Doctors usually treat HLHS with a three-step surgical "staged palliation" plan:

  1. The Norwood procedure: Usually done within the first 2 weeks of life. Surgeons build a new aorta and place a tube to the lung blood vessels called a shunt. This redirects the right ventricle's output to go to both the body and the lungs instead of going only to the lungs.

    For some babies, especially those born early or who have problems in other organs (besides the heart), the Hybrid procedure is done first. This helps to stabilize the baby before the Norwood procedure. The Hybrid procedure is less risky because it does not require open heart surgery.
  2. The bidirectional Glenn procedure (also called the hemi-Fontan procedure): Usually done between 4–6 months of age, this operation allows blood returning from the upper part of the body to flow directly to the lungs without passing through the heart. Now the right ventricle only has to do one job, pumping blood to the body.
  3. The Fontan procedure: Most often done between 18–36 months of age, this operation channels blood from the lower half of the body to the lungs. Now, blue blood returning from the entire body flows to the lungs without passing through the heart. When it reaches the lungs, the blood becomes oxygen-rich (red). The heart pumps this oxygen-rich blood to the body.

Treatment is called "palliative" because it helps the baby stay alive and grow, but does not completely correct the heart problems. In some cases, a heart transplant will be considered.

Medicines

The baby will get medicines, including prostaglandin, through tubes called intravenous (IV) catheters. The catheters usually are placed in the stub of the baby's umbilical cord.

Cardiac Catheterization

Several cardiac catheterization techniques can help with HLHS, such as inserting a wire mesh tube called a stent into the ductus arteriosus to keep it open.

Looking Ahead

Surgery does not cure HLHS, so problems can happen that require more surgery. Follow-up appointments with a pediatric cardiologist (a doctor who specializes in heart conditions) are essential.

A child who receives a heart transplant will need medicine throughout life to keep the immune system from attacking the transplanted heart.

Reviewed by: Gina Baffa, MD
Date reviewed: January 2018


Note: All information on KidsHealth® is for educational purposes only. For specific medical advice, diagnoses, and treatment, consult your doctor.

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