Hypoplastic Left Heart Syndrome
Also known as: HLHS
What is Hypoplastic Left Heart Syndrome (HLHS)?
Hypoplastic left heart syndrome (HLHS) is one of the most complex cardiac defects seen in newborns. Children diagnosed with hypoplastic left heart syndrome have all of the structures on the left side of the heart, which receive oxygenated blood from the lungs, severely undeveloped.
What are the signs/symptoms?
Babies with HLHS typically display the following:
- Lower than normal oxygen saturation
- Cyanosis, a blue skin color indicating a decrease in oxygen in the bloodstream
- Difficulty breathing (rapid breathing or shortness of breath)
- Low pulse
What causes HLHS?
Most of the time this heart defect occurs by chance, with no clear reason for its development
How is HLHS diagnosed?
Hypoplastic left heart syndrome is one of the most readily diagnosed on fetal echocardiograms and is one of the most common cardiac defects picked up on an obstetrical ultrasounds.
Treatment for Hypoplastic Left Heart Syndrome
Surgery for babies with HLHS will allow their heart to pump blood better to the lungs and the rest of the body. The surgery is conducted in three phases during the first few years of life.
- The first phase, called the Norwood procedure, is usually performed in the first weeks of life and includes the building of a new aorta.
- The second phase, called the Glenn operation, is usually performed between four and six months of age. This procedure connects the major vein carrying blood from the top half of the body directly to blood vessels to the lungs to get oxygen.
- The last phase, the Fontan procedure, is usually performed around three to four years of age. The exact procedures and timing depend on your child’s condition.