Total Anomalous Pulmonary Venous ReturnRegreso Total Anómalo de la Vena Pulmonar
Total Anomalous Pulmonary Venous Return
What is total anomalous pulmonary venous return?Total anomalous pulmonary venous return (TAPVR) is a congenital heart defect. This means that your child is born with it. It happens as the baby’s heart develops during the first 8 weeks of pregnancy.
In this condition, the 4 blood vessels (pulmonary veins) that carry oxygen-rich (red) blood to the heart from the lungs aren’t connected right. They should be connected to left chamber (atrium) of the heart. Instead, they’re connected somewhere else.
There are different types of TAPVR. The type your child has depends on where the pulmonary veins are connected.
This condition causes oxygen-rich blood from the lungs to mix with oxygen-poor (blue) blood from the body. This keeps oxygen-rich blood from being carried throughout the body. Your child cannot live with TAPVR long-term because he or she needs oxygen-rich blood throughout the body.
Other heart defects often occur with TAPVR. They actually help infants have enough oxygen in their blood until they can have surgery. These other defects include:
- Atrial septal defect. In this condition, an opening is between the two upper chambers of the heart (atrial septum). This causes oxygen-poor and oxygen-rich blood to be mixed.
- Open (patent) ductus arteriosus. The ductus arteriosus is a blood vessel that carries blood away from the heart in a developing baby. It usually closes soon after birth. If it stays open, it’s called patent ductus arteriosus. Sometimes it stays open with TAPVR. This causes oxygen-poor and oxygen-rich blood to be mixed.
What causes TAPVR?Most of the time, the cause of TAPVR isn’t known. It may occur with other heart or body system problems.
What are the symptoms of TAPVR?
The symptoms of TAPVR may be similar to symptoms of other conditions. Your child’s healthcare provider must diagnose him or her with this condition.
Newborns with TAPVR will have blue coloring of their skin, lips, and nailbeds (cyanosis). This happens in the first hours or days of their life. How severe your child’s condition is depends on how much blood is able to get to his or her body.
Other symptoms can occur a bit differently in each child. They can include:
- Fast breathing
- Trouble breathing
- Fast heart rate
- Cool, clammy skin
- Tiredness and little movement
- Poor feeding
How is TAPVR diagnosed?
A healthcare provider may first spot TAPVR in a baby during an ultrasound in pregnancy. After birth, if your child has signs of TAPVR, a pediatric cardiologist or neonatologist will check him or her. A pediatric cardiologist is a doctor with special training to diagnose and treat heart problems in babies and children. A neonatologist is a doctor with special training to diagnose and treat problems in newborns. These include babies born premature and full-term.
Next, your child’s doctor may do tests to check for heart problems. The tests your child needs depends on his or her age and condition. They also depend on the doctor’s preferences.
A chest X-ray may show changes in the heart and lungs caused by TAPVR.
An ECG records the electrical activity of the heart. It also shows abnormal rhythms (arrhythmias) and detects heart muscle stress. These problems may be caused by TAPVR.
This test uses sound waves to produce a moving picture of the heart and heart valves. An echo can show the structural changes of TAPVR.
A cardiac catheterization gives detailed information about the structures inside the heart. In this test, a small, thin, flexible tube (catheter) is put into a blood vessel in your child’s groin. Then the healthcare provider guides it to your child’s heart. A healthcare provider will inject your child with contrast dye to see the heart more clearly. Your child’s healthcare provider will give him or her medicine to help relax and prevent pain (sedation). Your child’s blood pressure and oxygen levels will be checked during the procedure. Your child may not need this test if a diagnosis is made during the echo.
How is TAPVR treated?
Treatment will depend on your child’s symptoms, age, and general health. It will also depend on how severe the condition is.
All children with an TAPVR will need to have surgery to fix it. Your baby may need to go into the neonatal intensive care unit (NICU) for treatment. TAPVR may also be treated through medical management and cardiac catheterization.
At first, your baby may get the following care:
- Supplemental oxygen or a machine that allows breathable air to move in an out of the lungs (ventilator). This helps with breathing.
- A medicine called prostaglandin E1. This is used to keep the ductus arteriosus open and allow blood to flow through the heart. This medicine isn’t used in some types of TAPVR.
- Medicine to help the heart
This test can be used to diagnose and treat some heart defects. To treat TAPVR, your child’s healthcare provider may do a test called balloon atrial septostomy. This test makes it easier for oxygen-rich blood to get to the rest of the body.
The surgery is done through a cut (incision) through the breastbone (sternum) and into the chest. Your baby will be connected to a heart-lung machine during surgery. This device does the work of your baby's heart and lungs during surgery. The details of the surgery depend on the type of defect your baby has. Your child’s heart doctor will explain the procedure to you.
What are the complications of TAPVR?The complications of TAPVR include:
- Enlarged heart
- Lung problems, including respiratory failure
- Heart failure
- Slowed growth and development
- Enlarged liver
Living with TAPVR
Your child will likely stay in the hospital until TAPVR is repaired. Your child’s healthcare team will give you instructions about special treatments or medicines your child needs before your child leaves the hospital. For instance, your child may need special formula and supplemental feedings to help with his or her growth. Your child’s healthcare team will also help you plan for home health care if you need it.
Many children with TAPVR will grow and develop normally after they have surgery. Most children don’t need to limit their physical activity. Your child will still need to see his or her heart doctor for regular checkups for the rest of his or her life. Your child’s follow-up care should be at a center that specializes in congenital heart defects. Ask your child's healthcare provider about your child’s outlook.
Your child may also need the following care:
- As children grow, they may need more heart repair procedures.
- Your child's heart doctor may give your child antibiotics before surgeries or dental procedures. This is to prevent infections. But this often isn’t needed.
- Some children are delayed in their development. Talk to your child’s healthcare provider about his or her development. Your child may need to be checked for issues.
When should I call my child's healthcare provider?If your child's skin, lips, or fingernails become blue or your child has trouble breathing or feeding, call your child's healthcare provider.
Key points about TAPVRIn TAPVR, the 4 blood vessels that carry oxygen-rich blood to the heart from the lungs aren’t connected right.
- This keeps oxygen-rich blood from being pumped to the body. Your child cannot live with TAPVR long-term because people need oxygen-rich blood throughout their body.
- All children with a TAPVR will need to have surgery. This is done to restore normal blood flow through the heart.
- Many children with TAPVR will grow and develop normally after they have surgery.
- Your child will need to see his or her heart doctor for regular checkups for the rest of his or her life.
Tips to help you get the most from a visit to your child’s healthcare 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.
- 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.