The Norwood procedure is primarily performed on infants born with Hypoplastic Left Heart Syndrome (HLHS). This surgery aims to enable the right side of the infant’s heart to pump oxygenated blood to the body, a function typically handled by the left side of the heart. In babies with HLHS, the left side of the heart is underdeveloped and unable to perform this crucial function.
After the Norwood procedure, the baby’s right ventricle (the lower chamber of the heart) continues its normal task of pumping deoxygenated blood to the lungs. Additionally, it assumes the role of the left ventricle in delivering oxygenated blood to the body. Unlike a normal heart, this setup does not maintain a strict separation between oxygenated and deoxygenated blood, which is an imperfect solution. Nevertheless, it significantly enhances oxygen delivery to the baby’s cells and tissues.
The three HLHS surgeries are as follows:
Babies diagnosed with hypoplastic left heart syndrome require early intervention, often within the first weeks of life, typically through procedures such as the Norwood operation. This surgery is critical because it allows the right ventricle to take on the combined workload of both ventricles, compensating for the underdeveloped left ventricle in these infants.
During the initial days after birth, the baby’s blood can naturally flow between the aorta and pulmonary artery via the patent ductus arteriosus, allowing the right ventricle to supply blood to both the lungs and the body. However, once this duct closes shortly after birth, the right ventricle can no longer effectively supply blood to the body.
Medication can temporarily keep the ductus arteriosus open. Nevertheless, the Norwood procedure serves as an interim solution, enabling the functional ventricle (typically the right one) to manage all pumping duties of the heart.
Some infants may not qualify for a Norwood procedure due to factors such as premature birth, small size for their gestational age (SGA), or other significant health challenges. In these cases, pulmonary artery bands may be used to regulate blood flow to the lungs and improve circulation to the body.
Complications from the Norwood operation include:
If your baby is diagnosed with hypoplastic left heart syndrome, they will receive medication shortly after birth to prevent the closure of the patent ductus arteriosus, a normal process. Keeping this duct open allows for increased blood flow through the heart until they undergo Norwood heart surgery.
In addition, a doctor may perform a septostomy to enlarge an opening between the two upper chambers of the heart (the right and left atria), improving the flow of blood from the lungs into the right side of the heart.
A Norwood procedure is a complex surgical operation involving several critical steps. Here is a simplified outline of what the surgeon will do:
The Norwood procedure is a lengthy surgery, often lasting as long as a full workday.
After surgery, your baby will initially receive care in the Intensive Care Unit (ICU). They typically spend about a week there before moving to a regular hospital room.
During their stay, you’ll notice various tubes and equipment designed to provide necessary support. Your baby will have a chest bandage following the Norwood procedure.
While the surgery improves blood circulation, it doesn’t cure the underlying condition. Mixing of oxygenated and deoxygenated blood can still occur in their heart, which may result in a persistent bluish tint to their skin.
Your doctor will provide detailed instructions for caring for your baby at home. Many hospitals offer specialized clinics for follow-up care, often including a home monitoring program. It’s beneficial to find a program that provides comprehensive, multidisciplinary care throughout your child’s development into adulthood.
Following surgery, your child will typically spend between seven to 21 days in the hospital, with a portion of this time in the intensive care unit.
In-hospital survival rates following the Norwood procedure are approximately 90%. Five-year survival rates range from 60% to 75%. Unfortunately, some children with HLHS may experience sudden fatal complications before they can undergo the second surgery.
Six years after surgery, about 60% of children survive without needing a heart transplant, a rate that remains stable at around 20 years post-surgery.
Babies with lower birth weight, premature birth, or other congenital disorders not related to the heart generally have a poorer prognosis following surgery