Patent Ductus Arteriosus (PDA)

Patent ductus arteriosus (PDA) is a heart defect found in the days or weeks after birth. The ductus arteriosus is a normal blood vessel that's part of fetal blood circulation before a baby is born. It’s an extra blood vessel that connects two arteries: the pulmonary artery and the aorta. The pulmonary artery carries blood from the heart to the lungs. The aorta carries blood from the heart to the body. Before birth, the ductus arteriosus lets blood go around (bypass) the lungs. This is because the baby gets oxygen from the mother through the placenta.

All babies are born with this opening between the aorta and the pulmonary artery. But it often closes on its own shortly after birth, once the baby breathes on their own and inflates their lungs. If it stays open (patent), it's called patent ductus arteriosus. With PDA, extra blood flows to the lungs. If the PDA is large, too much blood goes to the lungs. The blood vessels and the lungs have to work much harder to handle the extra blood. This can lead to fluid buildup in the lungs. The baby can have a harder time breathing and feeding.

PDA occurs twice as often in girls as in boys.

Experts don't know exactly why PDA occurs. It's more common in babies born prematurely. PDA can also occur along with other heart defects.

The size of the opening between the aorta and the pulmonary artery will affect symptoms. If your baby has a small opening, they may not have symptoms. If your baby has a larger opening, they may have symptoms. These are the most common symptoms of PDA:

• Skin that turns a blue color from not getting enough oxygen (cyanosis)

• Tiredness

• Fast or hard breathing

• Trouble feeding, tiredness while feeding, or sweating during feeding

• Infections

• Poor weight gain

• Frequent respiratory infections

• In older children, trouble doing activities

The symptoms of PDA can seem like other health conditions. Have your child see their health care provider for a diagnosis.

The provider will ask about your baby’s symptoms and health history. They will give your baby a physical exam. The provider may find a heart murmur or other symptoms during an exam. The provider may refer your baby to a pediatric cardiologist. This is a provider with special training to diagnose and treat heart problems in children.

The cardiologist will also check your baby and listen to the heart and lungs. The details about the heart murmur will help the provider make the diagnosis. Your baby may need tests, such as:

• Echocardiogram (echo). An echo uses sound waves to make a moving picture of the heart and heart valves. An echo shows the blood flow pattern through the PDA. It also shows how large the opening is and how much blood is passing through it. An echo is the most common way that a PDA is diagnosed.

• Chest X-ray. A chest X-ray may show an enlarged heart and lung changes in a baby with PDA.

Treatment will depend on your child’s symptoms, age, and general health. It will also depend on how severe the condition is.

A small PDA will often close on its own as your child grows. A PDA that causes symptoms will need to be treated with medicine, cardiac catheterization, or surgery. The cardiologist will check from time to time to see if the PDA is closing on its own. If a PDA does not close, it will be fixed to prevent lung problems. Treatment may include the following.

If not treated, PDA may lead to long-term lung damage. It can also damage the blood vessels in the lungs. But this is not common because most children will have been treated for their PDA before the lungs and blood vessels get damaged.

• If your child is discharged home before having a repair procedure, you will be shown how to feed and give medicine to your child. You will also be taught what symptoms to report to your child's provider.

• When your child is discharged after the PDA repair, you may give them pain medicine such as acetaminophen or ibuprofen to keep them comfortable. Your child's cardiac team will talk about pain control before your child goes home.

• Often infants who fed poorly before surgery have more energy once they recover. They begin to eat better and gain weight faster.

• Within a few weeks after surgery, older children are often fully recovered and able to do normal activities.

• You will get other instructions from your child's cardiac team and the hospital staff.

• In premature infants, the outlook after PDA surgical repair depends on gestational age and overall health.

• In children born full-term, early diagnosis and repair of PDA lets them live normal, healthy lives. Activity levels, appetite, and growth should return to normal. Your child's cardiologist may advise that your child take antibiotics to prevent infection in the heart lining and valves (bacterial endocarditis).

• In children with large PDAs diagnosed very late or never repaired, the outlook is uncertain. They are at risk for increased blood pressure in the blood vessels of the lungs (pulmonary hypertension). These children should get follow-up at a care center that specializes in congenital heart disease.

• Talk with your child's cardiologist about your child’s outlook.

Call your child's provider if your child's symptoms get worse or if new symptoms develop, especially breathing or feeding problems.

• PDA is a heart defect found in the days or weeks after birth.

• It occurs because a normal fetal connection between the aorta and the pulmonary artery does not close as it should after birth.

• PDA happens most often in premature infants. It often occurs with other congenital heart defects.

• A small PDA may close on its own as your child grows. If it is large or does not close, your child will need a repair procedure.

• An infant or child with PDA will be cared for by a pediatric cardiologist.

• Most children with a fixed PDA will live normal, healthy lives.

Tips to help you get the most from a visit to your child’s provider:

• Know the reason for the visit and what you want to happen.

• Before your visit, write down questions you want answered.

• At the visit, write down the name of a new diagnosis and any new medicines, treatments, or tests. Also write down any new instructions your provider gives you for your child.

• Know why a new medicine or treatment is prescribed and how it will help your child. Also know what the side effects are and when they should be reported.

• Ask if your child’s condition can be treated in other ways.

• Know why a test or procedure is recommended and what the results could mean.

• Know what to expect if your child does not take the medicine or have the test or procedure.

• If your child has a follow-up appointment, write down the date, time, and purpose for that visit.

• Know how you can contact your child’s provider after office hours. This is important if your child becomes ill and you have questions or need advice.