Hypoplastic Right Heart Syndrome
Hypoplastic right heart syndrome (HRHS) is the underdevelopment of the right side of the heart, particularly the ventricle. The ventricle is the muscular lower chamber of the heart.
Normally, the right ventricle pushes blood out of the heart and to the lungs where it can pick up oxygen. The blood with oxygen then moves to the left side of the heart which pumps the blood to the rest of the body.
HRHS makes it difficult or impossible to pass blood to the lungs. This decreases the amount of oxygen for the rest of the body. The underdeveloped muscle of the right ventricle can also be easily exhausted by normal heart functions.
Other structures of the right side of the heart may also be underdeveloped and decrease the flow of blood from the heart to the lungs. Structures that may be affected include:
- Tricuspid valve—Tissue that manages blood flow between the upper and lower chambers of the heart. If the valve does not exist or does not open it is called tricuspid atresia.
- Pulmonary valve—Tissue that manages flow of blood out of the heart to the pulmonary artery. If the valve does not exist or does not open it is called pulmonary atresia.
- Pulmonary artery—Blood vessel that carries the blood from the right ventricle to the lungs. The artery may be underdeveloped as well.
- Atrium—The top chamber of the heart.
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A fetus does not need to rely on their lungs for oxygen so blood flow to the lungs is not important. The mother’s blood will provide all the oxygen they need. However, after birth the lungs provide oxygen and poor blood flow to the lungs will begin to cause:
- Blue tint to skins and lips
- Rapid breathing
- Feeding problems
Certain structures of the heart and related blood vessels are present before birth. These structures decrease blood flow to the lungs. After birth, the baby will need to supply its own oxygen through the lungs. These structures gradually close over the first few weeks of life to increase the flow of blood to the lungs. Structures include:
- Ductus arteriosus—a connection between the pulmonary artery and the aorta (a large blood vessel that carries blood with oxygen away from the heart to the body)
- Foramen ovale—opening between the right and left side of the heart
These structures can decrease the efficiency of a normal heart. However, these structures actually help compensate for shortcomings created by HRHS. Symptoms of HRHS may worsen over the first few weeks of life as these structures close.
HRHS may be diagnosed before birth with prenatal ultrasound. The doctor may notice a size difference between the right and left side of the heart. A fetal echocardiogram may be done to confirm the diagnosis. An echocardiogram takes images of the heart in motion and can show structural and functional abnormalities.
After birth, HRHS may be suspected based on the baby’s symptoms. The doctor may also hear a heart murmur, which is the sound of turbulent blood flow. Your baby may be referred to a pediatric cardiologist. An echocardiogram may be used to examine the heart.
Babies with HRHS will need treatment shortly after birth. If HRHS was detected before birth, a team of specialists will help monitor and treat the baby immediately after birth. The course of later treatment will depend on the baby’s overall health and parental choice.
Medicine may be given shortly after birth to help keep the ductus arteriosus open. This and other openings will provide some relief until surgery can be done.
This procedure is often done within the first few days of life. It will help to increase the flow of blood to the lungs.
A tube, called a shunt, is attached from the pulmonary artery to the aorta (major blood vessel that carries blood from the left side of the heart to the body). Some blood can then move from the aorta to the pulmonary artery which carries the blood to the lungs. This increases the amount of blood that passes the lungs. The oxygen available for the body will increase as a result.
The shunt is a temporary measure to improve oxygen supply to the body and relieve symptoms such as blue tint to skin.
Glenn and Fontan Procedures
As the child ages, the shunt will not be able to provide enough blood flow to the lungs. Glenn and Fontan procedures may be done once the child is around age 3 months. The procedures are often split into 2 separate surgeries.
Blood returns from the body to the right side of the heart through major blood vessels called inferior and superior vena cava. The Glenn shunt creates a connection between the superior vena cava and the pulmonary arteries. This allows blood returning to the heart from the upper part of the body to bypass the right side of the heart and go directly to the lungs.
The Fontan or Fontan completion is done when the child is age 3-5 years. It creates a connection between the inferior vena cava and superior vena cava. This means all the blood returning from the body will go directly to the lungs and bypass the right side of the heart.
The shunts will help improve the amount of oxygen in the blood and reduce symptoms. However, surgery cannot repair the damaged right ventricle. Eventually, the left side of the heart will have difficulty keeping up with the extra workload. The heart will eventually need to be replaced with a heart transplant.
A heart transplant may be done early in childhood instead of the Glenn and Fontan procedures or late in adulthood when the heart is no longer able to properly function.
This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.
Edits to original content made by Denver Health.
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American Heart Association http://www.heart.org
GARD—Genetic and Rare Diseases Information Center https://rarediseases.info.nih.gov
About Kids Health—The Hospital for Sick Children http://www.aboutkidshealth.ca
Canadian Cardiovascular Society http://www.ccs.ca
Blalock-Taussig (BT) shunts. About Kids Health—The Hospital for Sick Children website. Available at: http://www.aboutkidshealth.ca/En/ResourceCentres/CongenitalHeartConditions/TreatmentofCongenitalHeartConditions/SurgicalCorrectionofCongenitalHeartDefects/Pages/Blalock-Taussig-BT-Shunts.aspx. Updated December 11, 2009. Accessed September 15, 2017.
Hypoplastic right heart syndrome. GARD—Genetic and Rare Diseases Information Center website. Available at: https://rarediseases.info.nih.gov/diseases/2922/hypoplastic-right-heart-syndrome. Updated June 18, 2013. Accessed September 15, 2017.
Norwood, Glenn and Fontan procedures. Children’s Healthcare of Atlanta website. Available at: https://www.choa.org/medical-services/cardiac-care/cardiothoracic-surgery-program/norwood-glenn-and-fontan-procedures. Accessed September 15, 2017.
Single ventricle defects. American Heart Association website. Available at: http://www.heart.org/HEARTORG/Conditions/CongenitalHeartDefects/AboutCongenitalHeartDefects/Single-Ventricle-Defects%5FUCM%5F307037%5FArticle.jsp#.WbwA3bKGNxA. Updated September 12, 2017. Accessed September 15, 2017.
Tricuspid atresia. EBSCO DynaMed website. Available at: https://www.dynamed.com/condition/tricuspid-atresia . Updated May 11, 2017. Accessed Updated September 15, 2017.
When your child has hypoplastic right ventricle: tricuspid atresia. Fairview website: https://www.fairview.org/patient-education/89171. Accessed September 15, 2017.