Double outlet right ventricle (DORV) is a congenital heart defect. There is a malformation of the fetal heart in the uterus leading to the right ventricle that has the two major arteries, namely the aorta and pulmonary artery arising from it.
Normal hearts have four chambers: two atria on top and two ventricles on the bottom. Two major blood vessels, or “great” arteries, normally connect to the ventricles.
With DORV, both great arteries connect to the right ventricle — either totally or in part. The left ventricle has just a part of either of the great arteries, or no artery at all.
Depending on the connections to the right ventricle, the body could receive oxygen-desaturated blood or the lung could receive excessive blood flow. The heart has to work harder to make up for the shortfall. DORV can also cause too much blood to get pumped into the lungs. This extra flow can damage both the heart and the lungs.
DORV is rare. It happens just once for every 6,000 to 10,000 newborns.
Babies with DORV always have a ventricular septal defect (VSD), too. VSD is a hole in the septum, the wall between the two ventricles. Blood flows through the hole and between the ventricles. The other possible associated anomaly is pulmonary valve stenosis.
Healthcare providers classify DORV by the location of the hole:
Scientists don’t completely understand what causes DORV. In some cases, it happens to babies who have problems with their chromosomes, the cell structures that hold their DNA.
Symptoms of DORV usually appear during the first days or weeks after birth. They’re like symptoms of other congenital heart problems and include:
Babies with DORV often have other congenital problems:
Sometimes healthcare providers can find a heart defect before a baby is born. They may do so during a routine ultrasound screening called a fetal echocardiogram.
If not, DORV is usually diagnosed in the days or weeks after birth because the baby has symptoms.
Sometimes a healthcare provider spots DORV before a baby is born. In other cases, the first signs of a heart problem get noticed with birth. Either way, the baby needs an exam:
Then the healthcare provider may order one or more tests:
Almost all babies with DORV need open-heart surgery within the first year of life. Your healthcare provider will help you make decisions about surgery by considering:
The surgeon may take one of the following approaches:
There is no way to prevent DORV. Scientists are still trying to understand its cause.
Without surgery, a baby with DORV will eventually develop:
With biventricular repair, people often live a normal life, with at least an average lifespan. People who needed other procedures may have shorter lifespans, and they may need further surgery later in life. Anyone who’s had surgery for DORV needs lifelong care from a cardiologist.
Most babies have good outcomes from surgery for DORV. But any heart surgery has risks, such as:
A note from Cleveland Clinic
Double outlet right ventricle is a serious condition that happens when the heart doesn’t develop correctly in the womb. While it can lead to serious heart and lung problems, timely treatment can keep your baby safe. Surgery and regular checkups can help people born with DORV live healthier, longer lives.