Coming Soon: New Building for Children's Specialty Care
Our new Children's Health Specialty Clinics building will bring 30 pediatric specialties together under one roof, making it easier for families to get expert care.
Truncus arteriosus is a heart defect that is present at birth (congenital). It happens when there is an abnormal connection between the aorta and pulmonary artery. Normally, the aorta and the pulmonary artery are separate. In truncus arteriosus, both the aorta and pulmonary artery begin from a common blood vessel.
Another congenital heart defect that nearly always happens with this condition is a ventricular septal defect (VSD). This is an abnormal hole in the wall (septum) between the two lower chambers of the heart (right and left ventricles).
In truncus arteriosus, oxygen-poor (blue) and oxygen-rich (red) blood mix through the VSD. The mixed blood that goes to the body does not have as much oxygen as it should.
Some congenital heart defects may occur more often in certain families. These are called genetic defects. Truncus arteriosus is often seen in babies born with 22q11.2 deletion syndrome. But in most cases, the cause is not known.
Symptoms of truncus arteriosus include:
The symptoms of truncus arteriosus can be like other health conditions. Have your child see their healthcare provider for a diagnosis.
A prenatal ultrasound may show truncus arteriosus. Your child's healthcare provider will check your child after birth. They may find signs like a pounding heart and weak pulse. They may hear an abnormal heart sound (heart murmur) when listening to your baby's chest with a stethoscope. If they do, you may have been referred to a pediatric cardiologist for a diagnosis. This is a healthcare provider with special training to diagnose and treat heart problems in babies and children.
These specialists will also examine your baby. They will listen to their heart and lungs with a stethoscope. Your baby may have other tests, including:
Treatment will depend on your child’s symptoms, age, and general health. It will also depend on how severe the condition is.
Truncus arteriosus must be treated with surgery to fix the defects. Typically surgery needs to occur during the first few days or weeks of life. But your child may need medical support until it is time for the operation to take place. Support may include:
Nutritional support may include:
Surgery is often done in the first few weeks after birth to prevent lung damage. The pulmonary arteries are separated from the aorta and reattached to the right ventricle. The pulmonary arteries may be reattached directly to the right ventricle typically using a conduit. The ventricular septal defect is also closed. Your child will stay in the hospital until after the surgical repair.
If not treated, truncus arteriosus may cause complications, such as:
Soon after surgery, babies have more energy and start to eat better and gain weight faster. But your baby may need high-calorie formula for several weeks or months after surgery. Your baby may also need tube feedings until they are able to feed better.
Your baby may become tired easily, and sleep more right after surgery. But in a few weeks, they should be fully recovered.
You may get other instructions from your child's cardiac team and the hospital staff.
Most children who have had truncus arteriosus surgical repair will live healthy lives. Their activity levels, appetite, and growth will often return to normal. Talk with your child's cardiologist about what activities and sports are safe for your child.
Your child most likely will need more surgery and/or cardiac catheterization procedures as they grow. Surgery in young adulthood may also be needed. These surgeries may involve replacing valves, repairing a narrowed aorta or pulmonary arteries, or replacing conduits.
The cardiologist may advise that your child take antibiotics before surgery or dental procedures. This is to prevent infection in the lining of the heart and heart valves (bacterial endocarditis).
Your child will need regular follow-up care at a pediatric or adult congenital cardiac care center throughout life.
Talk with the cardiologist about your child’s outlook.
Call your child's healthcare provider if your child has trouble breathing or feeding, or develops new symptoms.
Tips to help you get the most from a visit to your child’s healthcare provider:
Our new Children's Health Specialty Clinics building will bring 30 pediatric specialties together under one roof, making it easier for families to get expert care.