The treatment for congenital heart disease depends on the specific defect your child has.
Mild defects don’t usually need to be treated, although it is likely that you will have regular check-ups to monitor your health. More severe defects usually require surgery and long term surveillance of the heart afterwards throughout adult life by a congenital heart disease specialist.
In some cases, medications may be used to temporarily relieve symptoms or stabilise the condition before surgery.
These may include diuretics, to remove fluid from the body and make breathing easier, and digoxin, to slow your child’s heartbeat and increase the strength at which the heart pumps.
Types of congenital heart disease
Treatment plans for the following types of congenital heart defect are described below:
- aortic valve stenosis
- coarctation of the aorta
- Ebstein’s anomaly
- patent ductus arteriosus
- pulmonary valve stenosis
- septal defects – including atrial septal defects and ventricular septal defects
- single ventricle defects – including tricuspid atresia and hypoplastic left heart syndrome
- tetralogy of Fallot
- total anomalous pulmonary venous connection
- transposition of the great arteries
- truncus arteriosus
See types of congenital heart disease for descriptions of these defects.
Aortic valve stenosis
The urgency for treatment depends on how narrow the valve. Treatment may be needed immediately, or delayed until your child develops symptoms. If treatment is required, a procedure called a balloon valvuloplasty is often the recommended treatment option.
During this procedure a small tube (catheter) is passed through the blood vessels to the site of the narrowed valve. A balloon attached to the catheter is inflated, which helps to widen the valve and relieve any blockage in blood flow.
If balloon valvuloplasty is ineffective or unsuitable, it is usually necessary to remove and replace the valve using open heart surgery. This is where the surgeon makes a cut in the chest to access the heart.
Replacement valves are usually made from animal or human tissue if used in children, Metal valves are used in adulthood.
Coarctation of the aorta
If your child has the more serious form of coarctation of the aorta that develops shortly after birth, surgery to restore the flow of blood through the aorta is usually recommended.
Several surgical techniques can be used, including:
- removing the narrowed section of the aorta and reconnecting the two remaining ends
- inserting a catheter into the aorta and widening it with a balloon or metal tube (stent)
- removing sections of blood vessels from other parts of your child’s body and using them to create a bypass around the site of the blockage (this is similar to a coronary artery bypass graft which is used to treat heart disease)
If your child develops the less serious form of coarctation of the aorta in later life, the main goal of treatment will be to control their high blood pressure. This will usually involve using a combination of diet, exercise and, in some cases, medication. Read more about treating high blood pressure.
Ebstein’s anomaly
In many cases, Ebstein’s anomaly is mild and does not require treatment. However, surgery to repair the abnormal tricuspid valve is usually recommended if the valve is very leaky.
If valve repair surgery is ineffective or unsuitable, a replacement valve may be implanted. If Ebstein’s anomaly occurs along with an atrial septal defect (see below), the hole will be closed at the same time.
Patent ductus arteriosus
Many cases of patent ductus arteriosus (PDA) can be treated with medication shortly after birth.
Two types of medication have been shown to effectively stimulate the closure of the duct that is responsible for PDA. These are indomethacin and a special form of ibuprofen.
If PDA does not close with medication, the duct may be sealed with a coil or plug, which is implanted using a catheter.
Pulmonary valve stenosis
Mild pulmonary valve stenosis does not require treatment as it does not cause any symptoms or problems.
More severe cases of pulmonary valve stenosis usually require treatment, even if they cause few or no symptoms. This is because there is a high risk of heart failure in later life if it’s not treated.
As with aortic valve stenosis (see above), the main treatment for pulmonary valve stenosis is a balloon pulmonary valvuloplasty. However, if this is ineffective or the valve is not suitable for this treatment surgery may be needed to open the valve (valvotomy).
Septal defects
The treatment of ventricular and atrial septal defects depends very much on the size of the hole. No treatment will be required if your child has a small septal defect that does not cause any symptoms or stretch on the heart. These types of septal defects have an excellent outcome and do not pose a threat to your child’s health.
If your child has a larger ventricular septal defect, surgery is usually recommended to close the hole.
If there is a large atrial septal defect, this can be closed with an umbrella device inserted with a catheter. If the defect is too big or not suitable for the umbrella, surgery may be needed to close the hole. Unlike open heart surgery, the catheter procedure does not cause any scarring and is associated with just a small bruise in the groin. Recovery is very quick. This procedure is undertaken in specialist units which treat congenital heart problems in children and adults.
Single ventricle defects
Tricuspid atresia and hypoplastic left heart syndrome (HLHS) are treated in much the same way.
Shortly after birth, your baby will be given an injection of medication called prostaglandin. This will encourage the mixing of oxygen-rich blood with oxygen-poor blood. The condition will then need to be treated using a three-stage procedure.
The first stage is usually performed during the first few days of life. An artificial passage, known as a shunt, is created between the heart and lungs so blood can enter the lungs. However, not all babies will need a shunt.
The second stage will be performed when your child is four to six months old. The surgeon will connect veins from the upper part of the body, which carry oxygen-poor blood, directly to your child’s pulmonary valve. This will allow blood to be pumped into the lungs, where it can be filled with oxygen.
The final stage is usually performed when your child is 18 to 36 months old. It involves connecting the remaining veins to the pulmonary valve.
An effective alternative to this three-stage procedure would be to carry out a heart transplant, where a healthy heart is taken from a donor and surgically implanted into your baby. However, heart transplant surgery is rarely carried out in these circumstances because of a shortage of donated hearts that are suitable for a young baby.
Tetralogy of Fallot
Tetralogy of Fallot is treated using surgery. If your baby is born with severe symptoms, surgery may be recommended soon after birth. If the symptoms are less severe, surgery will usually be carried out when your child is three to six months old.
During the operation , the surgeon will close the hole in the heart and open up the narrowing in the pulmonary valve.
Total anomalous pulmonary venous connection
Total anomalous pulmonary venous connection (TAPVC) is treated with surgery. During the procedure, the surgeon will reconnect the abnormally positioned veins into the right place (the left atrium).
The timing of surgery will usually depend on whether your child’s pulmonary vein (the vein that connects the lungs and heart) is also obstructed. If the pulmonary vein is obstructed, surgery will be performed after birth. If the vein is not obstructed, surgery can often be postponed until your child is a few weeks or months old.
Transposition of the great arteries
As with treatment for single ventricle defects, your baby will be given an injection of medication called prostaglandin shortly after birth. This will prevent the passage between the aortic and pulmonary valve (the ductus arteriosus) closing after birth.
Keeping the ductus arteriosus open means that oxygen-rich blood is able to mix with oxygen-poor blood, which should help relieve your baby’s symptoms. In some cases, it may also be necessary to use a catheter to create a temporary hole in the atrial septum (the wall that separates the two upper chambers of the heart) to further encourage the mixing of blood.
Once your baby’s health has stabilised, it is likely surgery will be recommended. This should ideally be carried out during the first month of the baby’s life. A surgical technique called arterial switch is used. This involves detaching the arteries and reattaching them in the correct position.
Truncus arteriosus
Once your baby is in a stable condition, surgery is used to treat truncus arteroisus. This is usually carried out within a few weeks after birth.
The abnormal blood vessel will be split in two to create two new bloodvessels, and each one will be reconnected in the correct position.
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