Double-Inlet Left Ventricle

• The Heart Center team includes more than 40 pediatric cardiologists who diagnose and treat every kind of heart problem. We have treated many babies with this condition.
• Our doctors and surgeons are experts in the treatments your child may need. These may include surgery to change blood flow in your child’s heart, medicine and a heart transplant.
• Our 4 pediatric cardiac surgeons perform more than 500 procedures yearly. Our surgical outcomes are among the best in the nation year after year. See our outcomes for surgeries related to single-ventricle defects.
• We also have a pediatric cardiac anesthesia team and a Cardiac Intensive Care Unit ready to care for children who have heart surgery.
• Children with double-inlet left ventricle receive compassionate, comprehensive care through Seattle Children’s Single Ventricle Program. We bring together specialists in cardiology, nutrition, social work, feeding therapy and neurodevelopment to support your child’s health between surgeries.
• The transplant team does several heart transplants each year for children with this or other heart problems that cannot be controlled using other treatments. 
• Your child’s team includes experts from other areas of Seattle Children’s based on their needs, like doctors who specialize in newborns (neonatologists) or lung health (pulmonologists).

• If your developing baby is diagnosed with double-inlet left ventricle before birth, our Fetal Care and Treatment Center team works closely with you and your family to plan and prepare for any care your baby may need.
• Your child’s treatment plan is custom-made. We plan and carry out their treatment based on the specific details of their heart defect. We closely check your child’s needs to make sure they get the care that is right for them at every age.
• We have a special Adult Congenital Heart Disease Program to meet your child’s long-term healthcare needs. This program, shared with the University of Washington, transitions your child to adult care when they are ready.

• We are committed to your child’s overall health and well-being and to helping your child live a full and active life.
• Whatever types of care your child needs, we will help your family through this experience. We will discuss your child’s condition and treatment options in ways you understand and involve you in every decision.
• Our Child Life specialists know how to help children understand their illnesses and treatments in ways that make sense for their age.
• Seattle Children’s has many resources, from financial to spiritual, to support your child and your family and make the journey as smooth as possible.
• Many children and families travel to Seattle Children’s for heart surgery or other care. We help you coordinate travel and housing so you can stay focused on your child.
• Read more about the supportive care we offer.

Seattle Children’s is part of a nationwide group of children’s hospitals called the National Pediatric Cardiology Quality Improvement Collaborative (NPC-QIC). This group works to improve the outcomes and quality of life for children with double-inlet left ventricle. The NPC-QIC also offers resources, support and information for families.

Usually, doctors can diagnose double-inlet left ventricle when a baby is in the womb using a fetal echocardiogram (fetal echo). This is a special ultrasound that uses sound waves to view and make pictures of a developing baby’s heart during pregnancy. The results are interpreted by a pediatric heart doctor (cardiologist) who specializes in fetal congenital heart disease.

Your obstetrician may refer you for a fetal echo if your family has a history of congenital heart disease or if a routine prenatal ultrasound shows a problem.

Seattle Children’s Fetal Care and Treatment Center team can care for you when you are pregnant if your developing baby has a known or suspected problem.

To diagnose this condition, your child’s doctor will examine your baby, check their heartbeat and pulse and listen to their heart. In children with double-inlet left ventricle, doctors can often hear a heart murmur — the sound of blood moving in the heart in a way that’s not normal.

The doctor will ask for details about your child’s symptoms, their health history and your family health history.

Your child will need tests that provide more information about how their heart looks and works. These may include:

• Chest X-rays
• Cardiac catheterization
• MRI (magnetic resonance imaging)
• Echocardiography
• Electrocardiography

Babies born with double-inlet left ventricle usually have 3 surgeries during the first few years of life to change the blood flow through their heart: 

• Oxygen-poor blood, which returns from the body, is sent to blood vessels that go to the lungs.
• Oxygen-rich blood returns from the lungs into the working ventricle. This ventricle should be able to pump the oxygen-rich blood to the entire body.

The exact procedures and timing depend on your child’s condition and any other heart defects they have.

Your child may need medicines like these before and after surgery: 

• Angiotensin-converting enzyme (ACE) inhibitors, which lower blood pressure
• Digoxin, which makes the heart beat slower and with more force
• Anticoagulants, which help prevent or dissolve blood clots

Some children need a heart transplant. The heart transplant team at Seattle Children’s does many transplants each year for children with this or other heart problems that cannot be controlled with standard medical or surgical treatment. Read more about our Heart Transplant Program and our exceptional outcomes.

Outcomes for children with double-inlet left ventricle have improved greatly in the past several decades. Still, these babies are quite vulnerable between their first and second surgeries. They are at risk for serious health problems from common childhood illnesses, like colds, and they may have trouble feeding and growing. To provide care and closely check babies with double-inlet left ventricle, we see them through our Single Ventricle Program.