Topic Overview
What are congenital heart defects?
Congenital
			 heart defects are problems with how a baby's heart forms. "Congenital" means
			 that the heart problem develops before the baby is born or at birth.
Most
			 congenital heart defects affect how blood flows
			 through the
			 heart or through the blood vessels near the heart.
			 Some defects may cause blood to flow in a pattern that isn't normal. Others
			 can completely or partially block blood flow.
There are many
			 different types of congenital heart defects. They can be fairly simple, such as
			 a hole between the chambers of the heart or a heart valve that has not formed
			 right. Others are more serious and complex, such as a missing heart valve or
			 heart chamber.
Some defects are discovered in the fetus (developing baby)
			 while a woman is pregnant. Others are not found until birth. Still others may
			 not be discovered until your child gets older or even until he or she is
			 an adult.
No matter when a heart defect is discovered, having a
			 child with a heart problem is very stressful. Dealing with the fear and
			 uncertainty may seem overwhelming, especially when you have a fragile newborn.
			 It may help you to learn as much as you can about your child's treatment and to
			 talk to your doctor and other parents who have a child with similar
			 problems.
What causes the defects?
No one knows exactly what
			 causes most congenital heart defects. Genes passed down from a parent are a
			 possible cause. Viral infections also may play a role. For example, if a woman
			 gets German measles (rubella) while she is pregnant, it may cause problems with
			 how her baby's heart develops. Women who have
			 diabetes have a greater chance of having a child with
			 a congenital heart defect. 
Congenital heart defects are more
			 common in babies who are born with genetic conditions such as
			 Down syndrome.
Taking some prescription
			 or other medicines during pregnancy may cause congenital heart defects. Women who use  illegal "street" drugs or who drink alcohol during pregnancy have a
			 higher risk of having a baby with a congenital heart defect.
What are the symptoms?
Symptoms of congenital
			 heart defects will depend on what problem your baby has. Babies with congenital
			 heart defects may have one or more of these symptoms:
- Tiring quickly
- Difficulty breathing
- Puffiness
				or swelling
- Sweating easily
- Not gaining weight as they should
				
- A bluish tint to the skin, lips, and fingernails that
				becomes worse while eating or crying
- Fainting or near-fainting spells, especially related to
				physical activity
- Having dark, strong-smelling urine or other signs of dehydration
In some cases, your child's congenital heart defect may
			 be so mild that symptoms won't appear until the child is a teenager or young
			 adult.
How are congenital heart defects diagnosed?
In
			 most cases, congenital heart defects are found at birth or during a baby's
			 first few months.
You may find that your baby has trouble eating
			 or isn't gaining weight. Or your doctor may hear abnormal sounds or murmurs in
			 your baby's heart during a routine checkup. The first sign may be a bluish tint
			 to the baby's skin.
After a doctor suspects a heart defect, your
			 baby will probably need several tests, such as blood tests, an
			 echocardiogram, and possibly a heart catheterization.
			 The doctor may use the echocardiogram to check blood flow through your baby's
			 heart and to look at the valves, thickness, and shape of the heart. A heart
			 catheterization measures blood pressure in the heart and heart arteries and can
			 show how well the heart is pumping. 
Having your child go through
			 this testing can be very scary. Don't be afraid to ask as many questions as
			 you need to ask to feel comfortable. Talk to your doctor and the nurses. And talk to the
			 people who are doing the testing. 
How are they treated?
Some defects get better on
			 their own and may not need treatment. Your baby's or child's treatment will
			 depend on the type of defect.
Medicines may be used to help the
			 heart work better. Medicines may also treat symptoms until the defect is
			 repaired.
Some defects can be fixed by using a thin, flexible tube called a catheter. This procedure
			 doesn't require opening up the chest. The
			 doctor threads the catheter through a blood
			 vessel-typically in the groin-and into the heart. There, he or she uses the catheter to close holes or
			 open narrowed blood vessels or valves.
 If a baby has a large or
			 complex defect, the baby may need one or more open-heart surgeries. The surgery
			 may be done right away, done over several steps, or delayed until the baby is
			 stronger. Sometimes surgery is delayed if the baby is premature or until the
			 baby is strong enough to handle the surgery. In some cases, the child may need
			 different types of surgery over time as he or she grows.
In rare
			 cases, a heart defect may be so serious that a heart transplant is
			 needed.
Frequently Asked Questions
| Learning about congenital heart defects: |  | 
| Being diagnosed: |  | 
| Getting treatment: |  | 
| Ongoing concerns: |  | 
| Living with congenital heart defects: |  | 
Cause
The exact cause of most
		  congenital heart defects is not known. But doctors do
		  know that certain things increase the risk that a baby will have a heart
		  defect. See What Increases Your Risk.  
Symptoms
Congenital heart defects cause a wide range of symptoms. Your baby may have only mild
		  symptoms and tire easily, for example. He or she may have life-threatening
		  symptoms, such as
		  severe difficulty breathing. Or your baby may not have
		  any symptoms that you notice at birth but may have them later as he or she
		  grows. 
Symptoms usually go away after the defect is corrected. A
		  congenital heart defect that is repaired at the right time is less likely to
		  permanently affect your child's growth and development. 
Common symptoms include:
- Difficult or rapid  breathing.
			 You may notice trouble breathing when your baby is active, such as when he or she feeds or cries. Your baby may also breathe fast during rest or activities.
- Poor weight gain. When most of a
			 baby's energy is spent pumping blood to the body, little is left for eating and
			 growing. Your baby may tire when eating and may take longer than expected to
			 finish feeding. 
- Sweating, especially
			 on the head. You may notice that your baby has damp hair and cool, moist skin.
			 
- Fatigue and fussiness. Your baby may be too
			 tired to play and may sleep most of the time.
- Sudden weight gain or
			 puffiness and swelling of the skin, seen most often around the eyes and in the
			 hands and feet. These symptoms may be most noticeable when your baby first wakes up. The
			 weight gain or puffiness can be caused by fluid retention that is related to
			 poor blood circulation.
- Dehydration. Signs of dehydration include having dry mouth and eyes and having dark and strong-smelling urine.
Symptoms of blood flow problems
Blood flow problems caused by heart defects can mean that
		  your baby gets less oxygen. This happens mostly in children who have
		  cyanotic heart defects ("blue babies"). 
 If a baby has trouble getting oxygen or the heart is working extra hard, symptoms include:
- A bluish tint (cyanosis) to
			 the skin, lips, and nail beds. This becomes worse when your baby cries or eats.
			 
- Slower-than-expected growth and development (with more severe
			 congenital heart defects). Your baby may weigh less, be shorter, and take
			 longer than expected to learn skills such as standing and walking. 
What Happens
Congenital heart defects happen when the heart doesn't form normally as the developing baby (fetus) grows in the uterus. Heart defects may
		  cause problems with
		  blood flow through the heart after a baby is born. The problems can affect the
		  baby's blood and oxygen supply.
There are many types of congenital heart defects. If the defect lowers the amount of oxygen in the body, it is called cyanotic. If the defect doesn't affect oxygen in the body, it is called acyanotic. Some defects require treatment right away. Other defects get better on their own
		  and don't require treatment. 
Only about
		one-third of full-term babies born with a congenital heart defect have major defects
		that need surgery or have defects that may cause death during the first year of
		life.footnote 1
Not all defects are found when a child is very young. Some defects don't cause symptoms and aren't life-threatening. These defects may not
		  be found until the teen years or later.
Some children have a shorter life span than average if
			 their defect is severe or if heart failure or
		  other complications happen.
Long-term problems
 Many children and adults
		  with corrected heart defects lead healthy lives. But the treatments they've had or the defect itself can cause or be related to long-term problems. These include:
- Developmental delays or disabilities or
			 behavior problems.
- Certain physical
			 traits, such as smaller-than-average adult height and weight,
			 clubbing, or cyanosis (bluish tint to the skin from
			 low blood-oxygen levels). These can present challenges to a person's
			 self-esteem and confidence.
Adults
If you are an adult with a congenital heart defect, see the topic Congenital Heart Defects in Adults.
 You may
		  have to make decisions about things like:
- Pregnancy.
-  Birth control.
- Type of employment.
What Increases Your Risk
In most cases, the cause of a
		  congenital heart defect isn't known. But certain
		  things increase your baby's chances of having a heart defect.  These include:
- Family history. A child's risk for
			 having a congenital heart defect increases if a brother, sister, or parent has
			 one. 
- Other genetic conditions. For example,
			 Down syndrome has been linked to these
			 defects.
- Premature birth. Babies born too
			 early have a higher chance of having a heart
			 defect.
- Chronic conditions. Babies born to women with
			 diabetes or
			 phenylketonuria have a higher chance of having a
			 heart defect.
- Use of alcohol or drugs during the pregnancy. When a woman drinks alcohol or takes certain drugs while she is pregnant, her baby may develop a heart
			 defect.
If you're concerned about having a baby with a congenital heart defect, you can take steps to lower your
		  risk. For healthy pregnancy choices, see the topic Pregnancy.
When To Call a Doctor
Call  911  or other emergency services immediately if your child has
		  severe difficulty breathing, faints, or has
		  seizures.
Call your doctor immediately if your child
		  with a
		  congenital heart defect has:
- Symptoms of
			 heart failure or cyanosis-the bluish tint that affects
			 skin, lips, and nails because of lack of oxygen-that become significantly worse
			 within a short time period.
- Symptoms of
			 endocarditis, such as a fever that won't go
			 away.
- Symptoms of dehydration, such as sunken eyes with few tears, a dry mouth with little or no
			 spit, and little or no urine for 6 hours.
Talk to your doctor if your child with a congenital heart
		  defect has:
- Moderate difficulty
			 breathing.
- A poor appetite and isn't eating well, or sweats while eating, or has a
			 rapid heartbeat or rapid breathing while
			 eating.
- Less energy or seems to be sleeping more than
			 usual.
- Sudden weight gain or isn't gaining weight.
Who to see
The following health professionals can evaluate
			 symptoms of a congenital heart defect:
To prepare for your appointment, see the topic Making the Most of Your Appointment.
Exams and Tests
Testing a baby for
		  congenital heart defects can be done while a woman is
		  pregnant or after a baby's birth. Children and adults who have a heart defect need regular checkups throughout their lives.
Tests during pregnancy
A fetal
		  echocardiogram, which can be done as early as 16 weeks
		  of pregnancy, is the best test before a baby's birth. The test uses sound waves
		  to take pictures of the baby's heart. The fetal echocardiogram may be done if:
		  
-  The mother or father has a congenital heart defect.
- During her pregnancy the mother has
			 been exposed to certain chemicals.
- During her pregnancy the mother has
			 taken medicines that may increase the risk that her baby
			 (fetus) will develop heart defects.
- Other exams or tests show signs that a baby may have a
			 problem related to the heart's structure.
Tests after your baby is born
Many congenital heart defects are found in the first
		  month after a baby is born. Your doctor may ask about the baby's symptoms, appetite, and other habits. He or she may do other tests to find a heart problem, such as: 
More tests may be needed, depending on the symptoms and
		  type of defect. These may include:
- Chest X-ray,
			 to check the size and blood vessels of the heart.
- Electrocardiogram (ECG, EKG), to check for irregular
			 heart rhythms (arrhythmias) that may be related to a congenital heart defect.
			 
- Blood tests, to check for
			 anemia,
			 polycythemia, or levels of certain chemicals in the
			 blood.
- Oximetry, to see whether oxygen-poor
			 blood is being pumped to the body.  The amount of oxygen in the blood
			 can also be measured by an
			 arterial blood gas (ABG).
- CT scan or MRI of the heart and major blood vessels, to view
			 abnormal heart structures and/or blood vessels. During these tests, your
			 child will probably be given medicine to make him or her relax and sleep.
Tests for children and adults
Children, teens, and adults with congenital heart defects need regular checkups. They might have tests to check the health of the heart and to check for complications. 
A stress test (exercise electrocardiogram) can be done to check if a child or an adult with a heart defect needs exercise restrictions or to see if exercise performance is changing over time. This test might  be done before a child starts school or before a teen or adult starts a new exercise program.
Adults who have congenital heart defects need routine checkups. Be sure you have a primary care physician. You might also need to see your cardiologist regularly, such as once a year.
Early detection
If you are thinking of becoming pregnant and you or your partner has a congenital heart defect, it's best to plan ahead for a pregnancy. Genetic counseling  can help you find out your risk of passing a heart defect to your child. 
If you are already pregnant and you or your partner has a family history of congenital heart
			 defects, a fetal
		  echocardiogram or genetic testing may be done during pregnancy.
A baby may be checked for
			 congenital heart defects if:
Treatment Overview
 Your child's treatment for a
		  congenital heart defect will be based on the type of
		  problem he or she has. Your child's age, size, and general health also are
		  important. 
Your child may need:
- Medicines to help with symptoms. Some medicines
			 can control a heartbeat that isn't regular. Others make the heart stronger
			 until a defect can be fixed. Your child may need some medicines after
			 surgery. To learn more, see Medications. 
- A procedure called heart catheterization to find out details about the
			 heart defect or sometimes to repair the defect. To learn more, see Other Treatment. 
- Surgery to
			 repair the structural defect. If a newborn needs surgery, the
			 surgery may be delayed until the baby is stronger. If the defect threatens the
			 baby's life, surgery will be done right away. To learn more, see Surgery. 
Your child will also need regular visits to a pediatric cardiologist.
Coping
Caring for a child who has a heart problem can be
			 hard.
You may need to keep track of medicines and make frequent trips to
			 the doctor. Costs can be high. Try to
			 find support groups and other parents who can help you with the many emotions
			 involved.
What to think about
Some children die from severe congenital heart defects or related
			 complications, such as heart failure. If your baby is born with
			 a severe heart defect, there's a good chance that he or she
			 will survive with treatment. But you must also prepare for the possibility that
			 your child may die. Talk with your doctor about local resources and
			 organizations that can help you manage your emotional and practical
			 struggles when faced with this possibility.
Prevention
Congenital heart defects generally cannot be
		  prevented. 
If you or your partner has a congenital heart defect and you are planning to have a baby, see the topic Congenital Heart
		  Defects: Pregnancy.
Women who plan to get pregnant and women who are pregnant can lower their risk of having babies  with congenital
		  heart defects by taking steps to have healthy pregnancies. For healthy pregnancy choices, see the topic Pregnancy.
Home Treatment
Congenital heart defects often are repaired with surgery or heart catheterization, but home treatment also plays an important role. Some of the issues you'll face may include:
- Getting your child to eat enough.
- Giving medicines.
- Caring for a child in the hospital.
- Exercise restrictions.
- Coping with oxygen problems.
- Caring for yourself.
- Dealing with family issues and medical bills.
For more information and help, see Congenital Heart Defects: Caring for Your Child. 
Teens and adults who have heart defects may need to think  ahead about pregnancy, birth control, employment, and other issues. For help, see Congenital Heart Defects in Adults.
Medications
Medicines often are needed to treat
		  congenital heart defects until the defect can be
		  repaired or corrected. Some children and adults need to take medicine even after the defect is repaired. Children with certain defects that
		  cannot be completely corrected may have to take medicines for a long
		  time.
Treatment with medicines depends on the:
- Type of defect. Complex cyanotic heart defects usually need treatment with medicines more often than acyanotic heart defects. 
- Size of the defect. Children with large or complex defects are
				likely to have symptoms and may need medicines to relieve the symptoms.
Medicine choices
Medicines might be used to treat complications, relieve symptoms, or prevent problems. They might not treat the defect itself. 
The following are some of the medicines used for heart defects.
To treat complications and relieve symptoms
- Diuretics  lower the amount of extra fluid in the body.
- Digoxin increases the strength of the heartbeats.
- Vasodilators widen blood vessels so blood can flow more easily.
- Antiarrhythmics treat and prevent irregular heartbeats.
To treat a certain defect
To prevent problems
What to think about
Know how to give  medicine safely. Your child's heart medicines are very
			 strong and can be dangerous if they aren't given correctly. For help, see the topic Congenital Heart Defects: Caring for Your Child.
Surgery
Surgery is done for more complex defects or when
			 catheterization cannot correct the defect. Or your child might need a combination of surgery and catheterization to fix a defect. The kind of surgery will depend on what defect the child has. 
 Some congenital heart defects can be completely repaired
			 with one surgery. Defects that are more complex often require several surgeries over time. 
			 
Preparing for surgery
Prepare yourself for
		  what to expect at the hospital. It may be shocking to see your newborn or
		  child hooked up to so many machines and tubes. 
 If your child is older, you can help your child feel more
		  comfortable and secure by preparing him or her for what to expect. Your child's doctor or the hospital staff can help you prepare your child. Encourage your child to ask questions. And let him or her talk to the doctors too.
For more tips, see:
Surgery choices
In
		  general, the types of surgery are:
- Closing holes or blood vessels that have either formed or not
			 closed. Usually, a patch or stitches are used.
- Widening arteries.
-  Repairing or replacing valves that are too tight or that leak too much.
- Returning the aorta or pulmonary arteries to the
			 right position.
In rare cases, a heart transplant may be needed.
The type of surgery depends on the type of defect and the
			 surgeon's preference. 
What to think about
If a young baby (for example, newborn to age 3 months) has a life-threatening defect, surgery may be needed right away. For some
			 defects, the best time for surgery is before the child is 2 years old. For
			 other defects, the best time may be between the ages of 2 and 4.
 In some cases,
			 surgery may be done when a child is older. Surgery may be delayed if the defect
			 is likely to heal on its own.
Some types of surgery are more invasive and take longer to recover from than others. Even after
			 surgery, your child may still have symptoms such as weakness and a bluish tint
			 (cyanosis) to the skin, lips, and nail beds. 
After surgery, it's possible for symptoms to return or for complications to develop later. In these cases, more surgeries also may be needed.
Other Treatment
Heart catheterization may be used to correct certain
		  congenital heart defects. Children typically recover
		  more quickly from a heart catheterization procedure than from a surgery.
		  
With heart catheterization, a
			 doctor threads a thin, flexible tube called a catheter through a blood
			 vessel-typically in the groin-and into the heart. This lets the doctor check the heart and treat a defect.
Other Places To Get Help
Organization
National Heart, Lung, and Blood Institute (U.S.)
www.nhlbi.nih.gov
References
Citations
- Brown DW, Fulton DR (2011). Congenital heart disease in children and adolescents. In V Fuster et al., eds., Hurst's The Heart, 13th ed., pp. 1827-1883. New York: McGraw-Hill.
Other Works Consulted
- Brickner ME (2007). Congenital heart disease. In EJ Topol, ed., Textbook of Cardiovascular Medicine, 3rd ed., pp. 502-536. Philadelphia: Lippincott Williams and Wilkins.
- Brown DW, Fulton DR (2011). Congenital heart disease in children and adolescents. In V Fuster et al., eds., Hurst's The Heart, 13th ed., pp. 1827-1883. New York: McGraw-Hill.
- Feltes TF, et al. (2011). Indications for cardiac catheterization and intervention in pediatric cardiac disease: A scientific statement from the American Heart Association. Circulation, 123(22): 2607-2652.
- Giglia TM, et al. (2013). Prevention and treatment of thrombosis in pediatric and congenital heart disease: A scientific statement from the American Heart Association. Circulation, 128(24): 2622-2703. DOI: 10.1161/01.cir.0000436140.77832.7a. Accessed March 25, 2014.
- Madriago E, Silberbach M (2010). Heart failure in infants and children. Pediatrics in Review, 31(1): 4-12.
- Marino BS, et al. (2012). Neurodevelopmental outcomes in children with congenital heart disease: Evaluation and management. A scientific statement from the American Heart Association. Circulation, 126(9): 1143-1172.
- Sable C, et al. (2011). Best practices in managing transition to adulthood for adolescents with congenital heart disease: The transition process and medical and psychosocial issues: A scientific statement from the American Heart Association. Circulation, 123(13): 1454-1485.
- Warnes CA, et al. (2008). ACC/AHA 2008 Guidelines for the management of adults with congenital heart disease: Executive summary: A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation, 118(23): 2395-2451.
- Webb GD, et al. (2015) Congenital heart disease. In DL Mann et al., eds. Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 10th ed., vol. 2, pp. 1391-1445. Philadelphia: Saunders.
Credits
ByHealthwise Staff
Primary Medical ReviewerJohn Pope, MD - Pediatrics
Martin J. Gabica, MD - Family Medicine
E. Gregory Thompson, MD - Internal Medicine
Specialist Medical ReviewerLarry A. Latson, MD - Pediatric Cardiology
Current as ofSeptember 21, 2016