#1 Ranked Children’s Hospital by U.S. News & World Report
MyPatients provides referring primary care providers with secure access to their patients’ information.
Boston Children's has launched the world's 1st program dedicated to offering hand transplants to children who qualify.
Innovation insider is a semi-monthly e-newsletter analyzes innovations at Boston Children’s, other academic medical centers and from industry.
Read the latest blog by a Boston Children's doctor, clinician or staff member.
There are many ways you can help children and their families get the care they need.
It’s natural for you to be concerned right now about your child’s health—a diagnosis of pulmonary atresia can be overwhelming. But you can rest assured that at Boston Children's Hospital, your child is in expert hands.
There are two major variations in pulmonary atresia, usually characterized by the presence or absence of a hole (ventricular septal defect, or VSD) between the right and left ventricles:
Like many congenital heart conditions, pulmonary atresia isn’t a single defect, but rather a cluster of associated defects. Two additional holes usually close after birth, but are now important as temporary alternative openings for blood flow through the baby’s heart to his body and lungs:
Before birth, while the fetus is developing, pulmonary atresia isn’t a problem because the placenta provides oxygen for the baby. But once a baby is born, his lungs must provide the oxygen needed for survival. In children with pulmonary atresia, because there’s no opening on the pulmonary valve, blood cannot to get to the lungs and become oxygenated.
In PA, the abnormal development of the pulmonary valve prevents oxygen-poor (blue) blood from passing from the right atrium to the right ventricle and on to the lungs for oxygenation as it should. In this situation, blue blood will pass from the right atrium across the foramen ovale to the left atrium and ultimately out to the body, causing the characteristic “blueness” seen in babies with PA.
This situation is life-threatening, since the body requires oxygenated blood for survival, and oxygen-poor (blue) blood cannot meet the body’s demands.
Signs and symptoms of PA are clear shortly after a baby’s birth. The obvious sign of PA is a newborn who becomes cyanotic (blue) in the transitional first day of life, when the maternal source of oxygen (from the placenta) is removed. The degree of cyanosis is related to the presence of other defects that allow blood to mix, including a patent (open) ductus arteriosus.
Besides cyanosis (“blue baby syndrome”), the most common symptoms of pulmonary atresia are lethargy and pale, cool or clammy skin.
If your baby’s pediatrician notices any of these symptoms, the doctor may refer you to a pediatric cardiologist (and/or neonatologist) for immediate testing, diagnosis and a determination of treatment.
Most babies with PA show symptoms on the day they’re born. Others show symptoms in the first few days of life. If your newborn baby was born with a bluish tint to his skin, or if he’s having difficulty breathing, your pediatrician may refer you to a pediatric cardiologist (and/or neonatologist), who will perform a physical exam.
Your Boston Children’s cardiologist will detect a heart murmur, measure blood oxygen levels (non-invasively) and order diagnostic testing, which could include EKG, cardiac ultrasound, cardiac MRI, cardiac catheterization or chest x-ray. (PA is sometimes diagnosed before birth by a prenatal ultrasound done by your obstetrician.)
The heart starts to form during the first eight weeks of fetal development. In PA, during this development period the pulmonary valve doesn’t develop properly.
Some congenital heart defects may have a genetic link, either due to a defect in a gene or a chromosome abnormality—causing heart problems to occur more often in certain families. Most often, though, this heart defect occurs sporadically (by chance), with no clear reason for its development.
It’s important for parents to understand that you’ve done nothing to cause your baby’s pulmonary atresia and its accompanying defects. Nothing you’ve ingested or have been exposed to environmentally has been definitively be linked to having a baby with PA.
Treatment of pulmonary atresia with intact ventricular septum depends on the degree of undevelopment of the right ventricle (RV) and associated abnormalities. All babies with PA/IVS undergo cardiac catheterization to further define the heart’s anatomy. Some babies may be candidates for balloon dilation of the pulmonary valve in the catheterization lab.
In other babies, the RV may be too small, or associated abnormalities may exist that preclude opening the valve in the catheterization lab. Infants with this more severe form of PA/IVS are treated with a series of surgeries performed in the baby’s first few years. The goal of these surgeries is to re-route blood flow so that enough oxygen is added to the baby’s bloodstream to meet his body’s needs.
Your child most likely will be admitted to Boston Children’s cardiac intensive care unit (CICU) once symptoms are noted. Initially, he may be placed on oxygen, and possibly a ventilator, to help his breathing. We may give him IV (intravenous) medications to help his heart and lungs function more efficiently.
Important aspects of initial treatment—that allow time for the baby to stabilize —include the following:
Ultimately, for patients with a more severe form of PA/IVS, surgery will be necessary to improve permanent blood flow to the lungs. A series of three staged operations—called the Fontan sequence—may be needed, starting shortly after birth and concluding when a child is a few years old. The operations will redirect blood flow to the lungs and body through various surgical connections.
The outlook varies from child to child, but open heart surgery at Boston Children’s has among the highest success rates in the United States among large pediatric cardiac centers.
Your child may need multiple operations or catheterizations to replace conduits or revise a palliation as your infant grows older. After each procedure, your child will need to be followed by a Children’s pediatric cardiologist, who will make adjustments to medications, assist you with feeding problems, measure oxygen levels, and determine when/if it’s time for another procedure.
Note: Infants who’ve had initial surgery for a single ventricle defect are typically enrolled in Children’s Home Monitoring Program between the baby’s Stage I and Stage II operations in the Fontan sequence.
What is pulmonary atresia (PA)?
How common is PA?
If my child has PA/IVS, will he be OK?
How does Boston Children’s treat PA?
What are the symptoms of PA?
When is PA usually diagnosed, and how?
What should we do at home after PA surgery?
Will my baby be OK in the medium- and longer-term?
What is Boston Children’s’ experience treating congenital heart defects?
What heart research and innovations are coming from Boston Children’s?
Where can my child find care and support when he grows up?
Q: What is pulmonary atresia (PA)?
A: The pulmonary valve has three one-way leaflets that allow blood to flow into the pulmonary artery. With pulmonary atresia, abnormal valve development prevents these leaflets from opening; therefore, blood cannot flow forward from the right ventricle to the lungs to get oxygenated.
Back to top.
Q: How common is PA?
A: Pulmonary atresia affects one out of every 10,000 babies. While relatively rare, it’s the tenth most common form of congenital heart disease in newborns. It occurs slightly more often in boys than girls.
Q: If my child has PA/IVS, will he be OK?
A: Open heart surgery at Boston Children's Hospital has among the highest success rates in the United States among large pediatric cardiac centers. While very serious, pulmonary atresia is treatable surgically, and recent surgical advances have greatly improved your child’s outlook for success.
Q: How does Boston Children’s treat PA?
A: Initial stabilization of your baby usually happens with medications and catheterizations. In your baby’s first few years, the skilled surgeons at Boston Children’s will usually treat pulmonary atresia with a series of surgeries that re-route blood flow so that enough oxygen is added to the baby’s bloodstream to meet his body’s needs.
Q: What are the symptoms of PA?
A: Most babies with PA show symptoms on the day they’re born. Others show symptoms in the first few days of life. These include:
If your child has any of these symptoms, your pediatrician may refer you to a pediatric cardiologist for immediate testing, diagnosis and a determination of treatment.
Q: When is PA usually diagnosed, and how?
A: Most babies with PA show symptoms on the day they’re born. Others show symptoms in the first few days of life. If your newborn baby was born with a bluish tint to his skin, your pediatrician may refer you to a pediatric cardiologist (and/or neonatologist), who will perform a physical examination.
Your Boston Children’s cardiologist will detect a heart murmur, measure blood oxygen levels (non-invasively) and order diagnostic testing, which could include EKG, cardiac ultrasound, cardiac MRI, cardiac catheterization or chest x-ray. (Some PA may be diagnosed before birth by an ultrasound done by your obstetrician.)
Q: What should we do at home after PA surgery?
A: Consult your child’s cardiologist for guidance on follow-up care—including:
Your child may need multiple surgeries or catheterizations in his early years. As he recovers and grows, be sure to follow a regular program of well-baby/well-child checkups.
Q: Will my baby be OK in the medium and longer-term?
A: Your cardiologist will help you create a long-term care program as your baby matures into childhood, the teen years and even adulthood. Most people who have had congenital heart disease will have an ongoing relationship with their Boston Children’s cardiologist. We’ll prevent and treat complications, and will advise on daily-life issues, such as exercise and activity levels, nutrition and precautions related to pregnancy.
Surgical techniques for treating PA and its associated defects are continually being refined, and surgical success rates at Boston Children’s are very high. Nevertheless, your child will need lifelong monitoring and medication, since he may be at some risk for arrhythmias, infections, leaky valves, heart failure or stroke.
Non-cardiac surgeries and, for females, pregnancy do pose major risks and will require careful evaluation and discussion with a cardiologist.
Q: What is Boston Children’s’ experience treating congenital heart defects?
A: Boston Children’s surgeons treat some of the most complex pediatric heart conditions in the world, with overall success rates approaching 98 percent—among the highest in the nation among large pediatric cardiac centers.
Our experts have pioneered some of medical science’s most advanced heart treatments, now in use around the globe. Boston Children’s is among the only major pediatric heart centers in the world performing fetal heart interventions for certain congenital defects.
Q: What heart research and innovations are coming from Boston Children’s?
A: A significant amount of Boston Children’s groundbreaking cardiac research aims to refine and advance the open heart surgery and catheterization procedures that treat congenital heart defects in newborns and young children—including pulmonary atresia. Boston Children’s Cardiac Surgery Research Laboratory is studying the mechanisms of heart disease and new treatments for children with congenital heart defects.
Learn more about Boston Children’s cardiac research initiatives and Boston Children’s current projects in cardiology research.
Call your health care provider immediately if your baby or child is having difficulty breathing or is breathing rapidly, has a bluish color or seems to tire too easily.
After your child is diagnosed with PA, you may feel overwhelmed with information. It can be easy to lose track of the questions that occur to you. Lots of parents find it helpful to jot down questions as they arise—that way, when you talk to your child’s doctors, you can be sure that all of your concerns are addressed.
Some of the questions you may want to ask include:
Congenital heart defects usually occur sporadically (by chance), with no clear reason for their development. So, it’s difficult to predict who’s at risk. Familial cases have been reported, but no genetic link has been confirmed. In general, if you have a child with a congenital cardiac defect, the chance of other children you may have being born with a defect is about 2 to 3 percent.
The first children who underwent the staged surgical repairs for congenital heart defects are now in their 20s and largely doing well. However, complications can occur, including arrhythmias, blood clots, infections within the heart (endocarditis), leaky valves, easy tiring and loss of protein from the digestive tract. As he grows, it’s important for your child to be closely monitored by his cardiologist.
Surgical techniques for PA and its associated defects are continually being refined, and the long-term outlook is continually improving. Nevertheless, your child will need lifelong monitoring and possibly medication, since he may be at some risk for arrhythmias, infections, leaky valves, heart failure or stroke.
If you’re a teen with a congenital heart defect, you have a lot to cope with. Besides the typical issues any teenager faces—from social acceptance to body changes and more—you’ll also have to deal with medical appointments and procedures, some delay of your natural wish for independence, feeling different and assuming a lot of personal responsibility for maintaining your own good health.
If you feel overwhelmed, depressed or anxious through this important time in your transition to adulthood, speak to your doctor or counselor to get help.
If you were treated for congenital heart disease as a child, you’re probably being followed by your cardiologist, since complications from early heart disease can arise in adulthood.
You may need lifelong monitoring and medication, since you could be at some risk for arrhythmias, blood clots, infections, leaky valves, heart failure or stroke. Going forward, your cardiologist will advise you on activity levels, pregnancy issues and certain lifestyle choices.
Fortunately, Boston Children’s can help adults with congenital heart defects. Many adults who were patients at Boston Children’s as babies or children continue to be monitored by the clinicians who’ve followed them since childhood.
In addition, our Boston Adult Congenital Heart and Pulmonary Hypertension Service (BACH) provides long-term inpatient and outpatient care and advanced therapeutic options for patients with congenital heart disease and pulmonary hypertension as they reach and progress through adulthood.
BACH is an international center for excellence, with physicians and services from Boston Children’s, Brigham and Women’s Hospital and Beth Israel Deaconess Medical Center. The center promotes and supports clinical and scientific research for the advancement of care of these patients, and is a leader in the education of providers caring for this unique population.
After surgery, your child’s cardiologist will offer recommendations for follow-up care,
It’s important to understand that as parents, you’ve done nothing to cause PA and its accompanying defects, and there are no precautions you could have taken to prevent it. Congenital heart defects usually occur sporadically (by chance), with no clear reason for their development.
one of the heart’s two great arteries. In a normal heart, the aorta arises from the left ventricle and carries oxygen-rich blood out to the body.
atrial septal defect (ASD)
a congenital (present at birth) heart defect in which there is an opening in the tissue wall (septum) that divides the two upper chambers of the heart (right and left atria). A patent foramen ovale (PFO) is a type of ASD.
surgical procedure that frequently replaces the Blalock-Taussig shunt with another connection to the pulmonary artery to provide a path for blue blood to go out to the lungs. The superior vena cava is surgically connected to the right pulmonary artery to direct blood from the upper part of the body to the lungs to receive oxygen. This is the second procedure of the Fontan Sequence.
a surgical procedure to create a pathway for blood to reach the lungs. A shunt (tube) may be inserted between the aorta or one of its branches and pulmonary artery to increase blood flow. This is frequently the first procedure of the Fontan Sequence.
an invasive diagnostic procedure performed under sedation to obtain detailed visual information and measurements about the structures inside the baby’s heart. Blood pressure and oxygen measurements are taken in the four chambers of the heart, as well as the pulmonary artery and aorta. Cardiac catheterization can also be an interventional procedure. For some babies with PA, the pulmonary valve may be dilated in the catheterization lab.
pertaining to the heart
cardiac magnetic resonance imaging (MRI)
a non-invasive diagnostic tool using 3-D imaging technology produced by magnets to accurately determine the blood flow and functioning of your child's heart
a surgical procedure performed on the heart or one of the blood vessels connected to the heart
a doctor who performs surgery on the heart. A pediatric cardiac surgeon performs surgery on the hearts of infants and children.
a doctor who diagnoses and treats heart problems non-surgically. A pediatric cardiologist treats infants, children and some adults with heart problems.
a diagnostic tool to evaluate the size and spatial relationships of the heart within the child’s chest
blue color of skin, lips and nailbeds caused by a reduction in the amount of oxygen-rich (red) blood circulating in baby’s bloodstream
congenital heart defect
heart defect present at birth. The heart usually starts to form in the first eight weeks of fetal development. It’s thought that most congenital heart defects develop during this period.
medical determination of illness or disease based on history, physical examinations and advanced technology diagnostic testing tools
echocardiogram (echo, cardiac ultrasound)
An echocardiogram evaluates the structure and function of your child’s heart using electronically recorded sound waves that produce a moving picture of the heart and heart valves. If your baby has PA, the ultrasound will reveal the absence of a pulmonary valve and an underdeveloped right ventricle. No discomfort is involved. It takes 30-60 minutes. Some younger children may need to be sedated. If, during your pregnancy, a routine prenatal ultrasound or other signs raise your obstetrician’s suspicion of a congenital heart defect in the fetus, a cardiac ultrasound (described in the paragraph above) of the baby in utero will usually be the next step. The cardiac ultrasound—focusing exclusively on the baby’s heart—can usually detect whether a congenital heart defect is present.
a non-invasive test to measure the amount of oxygen in the blood
We are grateful to have been ranked #1 on U.S. News & World Report's list of the best children's hospitals in the nation for the third year in a row, an honor we could not have achieved without the patients and families who inspire us to do our very best for them. Thanks to you, Boston Children's is a place where we can write the greatest children's stories ever told.”