Diagnosis

Before birth

Because of advances in ultrasound technology, doctors can usually identify tricuspid atresia on a routine ultrasound exam during gestation.

After birth

Your baby's doctor might suspect a heart defect, such as tricuspid atresia, if your newborn has blue-tinged skin or is having trouble breathing.

Another indication is hearing a heart murmur, an abnormal whooshing sound caused by blood not flowing properly, when listening to your baby's heart during a physical exam.

If tricuspid atresia is suspected, your baby's doctor might order tests including:

  • Echocardiogram. This test uses sound waves that bounce off your baby's heart to produce moving images the doctor can view on a video screen. In a baby with tricuspid atresia, the echocardiogram reveals the absence of a tricuspid valve, irregular blood flow and other heart defects.
  • Electrocardiogram (ECG). This test records the electrical activity of the heart and can determine whether the heart's chambers are enlarged or the heart rhythm is abnormal.
  • Pulse oximetry. This measures the oxygen in your or your baby's blood using a sensor placed over the end of your or your baby's finger.
  • Chest X-ray. This might show whether the heart and its chambers are enlarged. It can also show whether there is too much or too little blood flow to the lungs.
  • Cardiac catheterization. A thin, flexible tube (catheter) is inserted into a blood vessel at your child's groin and guided into the heart. Rarely used to diagnose tricuspid atresia, this test might be used to examine the heart before surgery to treat tricuspid atresia.

Treatment

In tricuspid atresia, there's no way to replace a tricuspid valve. Treatment involves surgery to ensure adequate blood flow through the heart and into the lungs.

Often, this requires more than one surgery. Medications to strengthen the heart muscle, lower blood pressure and rid the baby's body of excess fluid and supplemental oxygen to help the baby breathe also might be given before surgery.

Surgery

Some of the procedures used to treat tricuspid atresia are a temporary fix to increase blood flow (palliative surgeries). Procedures that might be needed include:

  • Atrial septostomy. This creates or enlarges the opening between the heart's upper chambers to allow more blood to flow from the right atrium to the left atrium.
  • Shunting. This creates a bypass (shunt) from a main blood vessel leading out of the heart to the blood vessel leading to the lungs (pulmonary artery), which improves oxygen levels.

    Surgeons generally implant a shunt during the first two weeks of life. However, babies usually outgrow this shunt and might need another surgery to replace it.

  • Pulmonary artery band placement. If your baby has too much blood flowing to the lungs from the heart, a surgeon might place a band around the pulmonary artery to reduce the flow.
  • Glenn operation. When babies outgrow the first shunt, they often require this surgery, which sets the stage for the more-permanent corrective surgery, called the Fontan procedure.

    Doctors usually perform the Glenn operation when a child is between 3 and 6 months old. Doctors remove the first shunt, then connect one of the large veins that normally returns blood to the heart (the superior vena cava) to the pulmonary artery instead.

    This procedure allows blood to flow directly to the lungs and reduces the workload on the left ventricle, decreasing the risk of damage to it.

  • Fontan procedure. A variation of this standard treatment of tricuspid atresia is usually done when the child is 2 to 3 years old. In general, the surgeon creates a path for the blood that's returning to the heart (the inferior vena cava) to flow directly into the pulmonary arteries, which then transport the blood into the lungs.

    Doctors sometimes leave an opening between the pathway and the right atrium (fenestration).

Medication

Before surgery, your child's cardiologist might recommend that your child take the medication prostaglandin to help widen (dilate) and keep open the ductus arteriosus.

Follow-up care

To monitor heart health, you or your child will need lifelong follow-up care with a cardiologist who specializes in congenital heart disease.

Your or your child's cardiologist will tell you whether you or your child needs to take preventive antibiotics before dental and other procedures. In some cases, your child's cardiologist might recommend limiting vigorous physical activity.

The short- and intermediate-term outlook for children who have a Fontan procedure is generally promising. A variety of complications can occur over time and require additional monitoring and procedures.

Failure of the circulation system created by the Fontan procedure might make a heart transplant necessary.

Lifestyle and home remedies

Here are some tips for caring for your child with tricuspid atresia:

  • Strive for good nutrition. Your baby might not be getting enough calories because of tiring during feeding and an increased need for calories. It's often helpful to give your baby frequent, small feedings.

    Breast milk is an excellent source of nutrition, but formula works well, too. Your doctor might prescribe a special high-calorie formula.

  • Preventive antibiotics. Your or your child's cardiologist will likely recommend preventive antibiotics be taken before certain dental and other procedures to prevent bacteria from infecting the inner lining of the heart (infective endocarditis).

    Practicing good oral hygiene — brushing and flossing teeth, getting regular dental checkups — also helps prevent infection.

  • Stay active. Encourage as much normal play and activity as you or your child can tolerate or as your doctor recommends, with ample opportunity for rest. Staying active helps your or your child's heart stay fit.
  • Keep up with routine medical and well-child care. Standard immunizations are encouraged for children with congenital heart defects, as well as vaccines against the flu, pneumonia and respiratory syncytial virus infections. Your child should take all medications as prescribed.
  • Keep follow-up appointments with your or your child's doctor. Your child will need at least annual appointments with a doctor trained in congenital heart conditions. Your child's doctor is likely to recommend several tests to evaluate your or your child's heart condition.

Adults with tricuspid atresia

If you're an adult with tricuspid atresia, you need to be seen regularly throughout your life by a doctor trained in adult congenital heart conditions. Your doctor is likely to recommend regular tests to evaluate your condition at these appointments.

Your doctor might recommend that you take preventive antibiotics before certain dental or medical procedures to prevent infective endocarditis.

Ask your doctor about what activities are best for you, and if there are sports or activities that you should limit or avoid.

Tricuspid atresia and pregnancy

Women with tricuspid atresia who are considering pregnancy should talk to a doctor who specializes in adult congenital heart diseases as well as a maternal-fetal medicine specialist. If you do become pregnant, it's best to see a doctor who specializes in pregnancies in women with congenital heart disease.

For women who have had a Fontan procedure, pregnancy will be considered high-risk. Some women, such as those with a history of heart failure, will be discouraged from becoming pregnant.

Coping and support

Caring for a baby with a serious heart problem such as tricuspid atresia can be challenging. Here are some strategies that might help:

  • Try to maintain normalcy and closeness. Maintaining a regular daily routine will help both you and your child. Even if your baby is in the hospital, try to spend as much time together as you can. Include other children you have. Family bonding is important for your baby's social and emotional development.
  • Seek support. Ask family members and friends for help. Ask your child's cardiologist about support groups and other types of assistance. The American Heart Association offers a support group called Mended Little Hearts.
  • Record your baby's health history. Write down your baby's diagnosis, medications, surgery and other procedures and their dates, the name and phone number of your child's cardiologist, and other important information about your baby's care. It's also helpful to keep copies of surgical reports.
  • Talk about your concerns. As your child grows and develops, discuss your concerns about his or her health with your child's cardiologist.

Remember that many children with congenital heart defects, such as tricuspid atresia, grow up to lead full lives.

Preparing for your appointment

Eventually you or your baby will see a cardiologist with experience in treating congenital heart defects. Here's some information to help you get ready for the appointment.

What you can do

Make a list of:

  • Symptoms you've noticed in yourself or your child, including any that may seem unrelated to a heart defect
  • Important personal information, including family history of congenital heart disease, illnesses the mother had during pregnancy or behaviors, such as smoking, during pregnancy
  • Questions to ask your doctor

Take a family member or friend along, if possible, to help you remember the information your doctor gives you.

For a congenital heart defect, questions to ask the cardiologist include:

  • What tests are needed?
  • What treatments are available, and which do you recommend?
  • Will this require more than one surgery?
  • How can I make myself or my child more comfortable?
  • Are there restrictions to follow?
  • If I get pregnant again, is there a way to prevent this from happening again?
  • Are there brochures or other printed material that I can have? What websites do you recommend?

Don't hesitate to ask other questions.

What to expect from your doctor

Your doctor is likely to ask you questions, such as:

  • Have symptoms been continuous or occasional?
  • What, if anything, seems to improve the symptoms?
  • Does anything worsen the symptoms?