Learn more about this rare congenital heart condition that results in underdevelopment of the left side of the heart.
Hypoplastic left heart syndrome is a complex and rare heart defect present at birth (congenital). In this condition, the left side of the heart is critically underdeveloped.
If your baby is born with hypoplastic left heart syndrome, the left side of the heart can't effectively pump blood to the body. Instead, the right side of the heart must pump blood to the lungs and to the rest of the body.
Medication to prevent closure of the connection (ductus arteriosus) between the right and left sides, followed by either surgery or a heart transplant, is necessary to treat hypoplastic left heart syndrome. Advances in care have improved the outlook for babies born with this condition.
Babies born with hypoplastic left heart syndrome usually are seriously ill soon after birth. Signs and symptoms include:
If the natural connections between the heart's left and right sides (foramen ovale and ductus arteriosus) are allowed to close in the first few days of life in babies with hypoplastic left heart syndrome, they can go into shock and possibly die.
Signs of shock include:
A baby in shock might be conscious or unconscious. If you suspect your baby is in shock, immediately call 911 or your local emergency number.
It's likely that your baby would be diagnosed with hypoplastic left heart syndrome either before birth or soon after. However, you should seek medical help if you notice that your baby has any of the signs or symptoms of the condition.
If your baby has signs or symptoms of shock, call 911 or your local emergency number right away.
Hypoplastic left heart syndrome occurs when the baby's heart is developing in the womb. The cause is unknown. However, if your family has one child with hypoplastic left heart syndrome, the risk of having another with a similar condition is increased.
A normal heart has four chambers, two on the right and two on the left. In performing its basic job — pumping blood throughout the body — the heart uses its left and right sides for different tasks.
The right side moves blood to the lungs. In the lungs, oxygen enriches the blood, which then circulates to the heart's left side. The left side of the heart pumps blood into a large vessel called the aorta, which circulates the oxygen-rich blood to the rest of the body.
In hypoplastic left heart syndrome, the left side of the heart can't properly supply blood to the body because the lower left chamber (left ventricle) is too small or in some cases doesn't exist. In addition, the valves on the left side of the heart (aortic valve and mitral valve) don't work properly, and the main artery leaving the heart (aorta) is smaller than normal.
For the first days of life, the right side of the heart can pump blood both to the lungs and to the rest of the body through a blood vessel that connects the pulmonary artery directly to the aorta (ductus arteriosus). The oxygen-rich blood returns to the right side of the heart through a natural opening (foramen ovale) between the right chambers of the heart (atria). When the foramen ovale and the ductus arteriosus are open, they are referred to as being "patent."
If the ductus arteriosus and the foramen ovale close — which they normally do after the first day or two of life — the right side of the heart has no way to pump blood out to the body. In babies with hypoplastic left heart syndrome, medication is necessary to keep these connections open and keep blood flowing to the body until heart surgery is performed.
If you already have a child with hypoplastic left heart syndrome, you have a higher risk of having another baby with this or a similar condition.
Beyond family history, there are no clear risk factors for hypoplastic left heart syndrome.
Without surgery, hypoplastic left heart syndrome is deadly, usually within the first few days or weeks of life.
With treatment, many babies survive, although most will have complications later in life. Some of the complications might include:
There's no way to prevent hypoplastic left heart syndrome. If you have a family history of heart defects, or if you already have a child with a congenital heart defect, consider talking with a genetic counselor and a cardiologist experienced in congenital heart defects before getting pregnant.
It's possible for a baby to be diagnosed with hypoplastic left heart syndrome while still in the womb. Your doctor might be able to identify the condition on a routine ultrasound exam during the second trimester of pregnancy.
After your baby is born, a doctor might suspect a heart defect, such as hypoplastic left heart syndrome, if your baby has grayish-blue skin color or has trouble breathing. Your baby's doctor might also suspect a heart defect if he or she hears a heart murmur — an abnormal sound caused by turbulent blood flow — when listening to the heart with a stethoscope.
Doctors usually use an echocardiogram to diagnose hypoplastic left heart syndrome. This test uses sound waves that bounce off your baby's heart to produce moving images that can be viewed on a video screen.
If your baby has hypoplastic left heart syndrome, the echocardiogram will show a smaller than normal left ventricle and aorta. The echocardiogram might also show abnormal heart valves.
Because this test can track blood flow, it also shows blood moving from the right ventricle into the aorta. In addition, an echocardiogram can identify associated heart defects, such as an atrial septal defect.
Hypoplastic left heart syndrome is treated through several surgical procedures or a heart transplant. Your child's doctor will discuss treatment options with you.
If the diagnosis has been made before the baby is born, doctors usually recommend delivery at a hospital with a cardiac surgery center.
Your baby's doctor might recommend several options to help manage your baby's condition before surgery or transplant, including:
Your child will likely need several surgical procedures to treat hypoplastic left heart syndrome. Surgeons perform these procedures to create separate pathways to get oxygen-rich blood to the body and oxygen-poor blood to the lungs. The procedures are done in three stages.
Norwood procedure. This surgery is usually done within the first two weeks of your child's life. There are several ways to do this procedure.
Surgeons reconstruct the aorta and connect it to the heart's lower right chamber (right ventricle). Surgeons insert a tube (shunt) that connects the aorta to the arteries leading to the lungs (pulmonary arteries), or they place a shunt that connects the right ventricle to the pulmonary arteries. This method allows the right ventricle to pump blood to both the lungs and the body.
In some cases, a hybrid procedure is done. Surgeons implant a stent in the ductus arteriosus to maintain the opening between the pulmonary artery and aorta. Bands placed around the pulmonary arteries reduce blood flow to the lungs and create an opening between the atria of the heart.
After the Norwood procedure, your baby's skin will still have a blue coloring because oxygen-rich and oxygen-poor blood continue to mix within the heart. Once your baby successfully passes through this stage of treatment, the odds of survival can increase.
Bidirectional Glenn procedure. This procedure is generally the second surgery. It's done when your child is between 3 and 6 months of age. Doctors remove the first shunt attached to the pulmonary arteries, and then connect one of the large veins that normally returns blood to the heart (the superior vena cava) to the pulmonary artery instead. If surgeons previously performed a hybrid procedure, they'll follow additional steps during this procedure.
This procedure reduces the work of the right ventricle by allowing it to pump blood mainly to the aorta. It also allows most of the oxygen-poor blood returning from the body to flow directly into the lungs without a pump.
After this procedure, all the blood returning from the upper body is sent to the lungs, so blood with more oxygen is pumped to the aorta to supply organs and tissues throughout the body.
Fontan procedure. This surgery is usually done when your child is between 18 months and 4 years of age. The surgeon creates a path for the oxygen-poor blood in one of the blood vessels that returns blood to the heart (the inferior vena cava) to flow directly into the pulmonary arteries. The pulmonary arteries then transport the blood into the lungs.
The Fontan procedure allows the rest of the oxygen-poor blood returning from the body to flow to the lungs. After this procedure, there's minimal mixing of oxygen-rich and oxygen-poor blood in the heart, and your child's skin will no longer look blue.
After surgery or a transplant, your baby will need lifelong follow-up care with a cardiologist trained in congenital heart diseases. Some medications might be needed to regulate heart function. Various complications can occur over time and might require further treatment or other medications.
Your child's cardiologist will tell you whether your child needs to take preventive antibiotics before certain dental or other procedures to prevent infections. In some cases, the doctor might also recommend that your child limit physical activity.
As an adult, you'll transition from a pediatric cardiologist to a cardiologist trained in congenital heart disease in adults. Only recently have advances in surgical care resulted in children with hypoplastic left heart syndrome surviving into adulthood, so it's not yet clear the challenges an adult with the condition might face. You'll need regular, lifelong follow-up care to monitor for any changes in your condition.
Women considering pregnancy should discuss pregnancy risks and birth control options with their doctors. Having this condition increases your risk of cardiovascular problems during pregnancy, the risk of miscarriage and the risk of having a baby with congenital heart disease.
It can be challenging to live with hypoplastic left heart syndrome or to care for a baby with the condition. Here are some strategies that may help make it easier:
Seek support. If you have a child with hypoplastic left heart syndrome, ask family members and friends for help. It's important for caregivers to take breaks. Talk with your child's cardiologist about support groups and other types of assistance.
If you're a teen or an adult with hypoplastic left heart syndrome, ask your doctor if there are support groups for adults with congenital heart conditions. It can be helpful to talk to other people who share your challenges.
Record your or your baby's health history. Write down your or your baby's diagnosis, medications, surgery and other procedures and the dates they were performed, as well as the name and phone number of your or your child's cardiologist, emergency contact numbers for your or your child's doctors and hospital, and other important information about your or your baby's care. Include a copy of the operative report from your or your child's surgeon in your records.
This information will help you recall the care you or your child has received, and it will be useful for doctors who are unfamiliar with you or your baby to review the complex health history. This information is also helpful as your child grows into adulthood and transitions from pediatric to adult cardiology care.
Talk about your concerns. As your child grows, talk with the cardiologist about which activities are best for your child. If some are off-limits, encourage your child in other pursuits rather than focusing on what he or she can't do.
If other issues about your child's health concern you, discuss them with your child's cardiologist, too. As an adult, ask your doctor about what activities you can do, and about your concerns.
November 10th, 2021
