create your own

CHD - The Most Common Birth Defect

75
rate or flag this page

By Cari Jean


baby shortly after open heart surgery
baby shortly after open heart surgery

Congenital heart defects (CHD) are the most common birth defects. CHD affects 8 out of every 1,000 newborns. Each year, more than 35,000 babies in the United States are born with congenital heart defects. Congenital heart defects are also responsible for more deaths in the first year of life than any other birth defect.

What exactly is CHD?

Congenital Heart Defects are when babies are born with something wrong with their hearts. When some part of the heart doesn't develop normally, the flow of blood is changed through the heart. Some CHDs, like mild pulmonary valve stenosis (narrowing of the pulmonary valve) are simple defects and usually do not require treatment. The only symptom may be a heart murmur.

Other defects, however, can be more complex, such as tetralogy of fallot, which is the most common complex CHD. Tetralogy of fallot (TOF) consists of four different types of defects which prevents an adequate amount of blood from reaching the lungs, resulting in oxygen-poor blood flow to the body. In the case of this type of defect, open heart surgery is needed either at birth or later in infancy. Symptoms of TOF usually include cyanosis or blueness of the skin and/or mouth and fingernails.

Whether mild or complex, there are 35 known types of defects. Heart defects may involve missing, unconnected or misplaced arteries; underdevloped or missing valves, and narrowed or blocked blood vessels.


smoking has been linked to babies born with CHD
smoking has been linked to babies born with CHD

Causes of CHD

To date, there is no known cause of CHD. Researches have speculated that heart defects are caused by a genetic abnormality or when the developing fetus is exposed to infections, toxic substances or drugs. Other factors may include:

  • Hereditary - a parent with a congenital heart defect may be more likely to have a child with CHD.
  • Genetic Disorders - Children with genetic disorders are more likely to have CHD. Half of all Down Syndrome babies have heart conditions.
  • Smoking during pregnancy - smoking has been linked to several congenital heart defects
  • Babies born prematurely have a higher chance of having a congenital heart defect.
  • Babies born to women who have chronic conditions such as diabetes have a higher chance of having a congenital heart defect.

Symptoms of CHD

If a baby has a mild defect, there may be no symptoms at all. There may be a heart murmur which can be heard with a stethoscope but sometimes even healthy babies and children have heart murmurs and some of them even grow out of their murmur.

Some symptoms of CHD in babies and children include:

  • Rapid or difficulty breathing
  • Cyanosis
  • Tires easily
  • Poor circulation
  • Sweating
  • Poor weight gain
  • Sudden weight gain or puffiness or swelling of the skin

There are some types of heart defects that cause the heart to work harder than it should. If the heart continues to work too hard it could result in heart failure. This is also known as Congestive Heart Failure or CHF.

Symptoms of heart failure include:

  • Fatigue with physical activity
  • Shortness of breath
  • A buildup of blood and fluid in the lungs
  • A buildup of fluid in the feet, ankles, and legs


surgeons performing open heart surgery
surgeons performing open heart surgery

Treatments for CHD

Treatments for CHD vary depending on the severity of the heart defect and also the general health of the heart patient. As discussed earlier, mild defects might not require any treatment. While this is true, it is important to be seen by a pediatric cardiologist as he or she deems necessary. Some defects can get worse over time so it is always best to take extra caution.

Medication

Sometimes medication is required. Some examples of medicines used to treat CHD include:

  • Antiarrhythmics - controls irregular heartbeats
  • Cardiac glycosides - increases strength of heartbeats
  • Vasodilators - enlarges blood vessels
  • Diuretics - reduces extra fluid (usually used in cases of heart failure)
  • Prostaglandins and prostaglandin inhibitors - improves blood flow to the lungs or body

Catherization

Some who have CHD need to undergo a heart catherization. This is done in order to find out the details of the heart defect or to sometimes to repair it. With heart catherization, a catheter is threaded through a blood vessel, usually in the groin and into the heart. This procedure allows the doctor see how blood is flowing through the heart and heart arteries.

Surgery

Sometimes treatment includes surgery. The type of surgery depends on the type of heart defect. There are many different kinds of surgeries to treat several different heart defects. If the defect is life-threatening, surgery might be done right away in a newborn. For other defects, surgery is usually done within the first two years of the child's life. Sometimes a child has two, three or more surgeries within the first years of the child's life.

There are cases where all three types of treatment - medicine, catherization and surgery - may be required. Also, it is important to know that just because a child has had corrective surgery does not mean they are cured. A congenital heart defect is something the child is going to receive ongoing care for, or at least be seen by a pediatric or a congenital adult cardiologist on a regular basis.


I will give you a new heart and put a new spirit in you; I will remove from you a heart of stone and give you a heart of flesh. And I will put my spirit in you and move you to follow my decrees. Ezekiel 36:26-27a

My Heart Defect

I myself was born with a congenital heart defect called Double Outlet Right Ventricle (DORV), which is considered a very complex defect. When I was a baby, symptoms my mom noticed were tiring easily and cyanosis. I had my first heart surgery called a Waterston shunt at six months of age. At the time, my parents and older brother lived in Montana and they needed to take me (by car) all the way to Minneapolis for the surgery. When I was four, I had my second surgery called the BT shunt. We got to travel by train to Minneapolis for that one. And when I was ten I had the fontan. Post fontan, I was so excited to have pink fingernails and I took my first plane ride from the Twin Cities to Minot, ND.

The best way to describe my heart condition is that there are two main arteries attached to the ventricles. There is the pulmonary artery which carries oxygen-poor blood to the lungs and there is the aorta which carries oxygen-rich blood from the heart to the body. In a normal heart, the pulmonary artery rises from the right ventricle and the aorta rises from the left ventricle. In my heart, both the pulmonary artery and the aorta were attached to my right ventricle which caused my left ventricle to be non-functioning. Along with this, I also had pulmonary stenosis and a ventral septal defect.

It was hard being a kid with a heart defect because it meant I couldn't do many of the normal physical activites that kids do. Running was a huge no-no. When I did overextend myself I got really bad headaches, sometimes migraines. I was pale and cyanotic with blue lips and blue fingernails. I had scars on each side of my body and after my third surgery I had a scar down the middle of my chest. After my fontan when I was ten, I actually felt 'normal' and healthy and could do more things. It seemed I had been cured, until my bout with congestive heart failure when I was 19. That though, is another hub which I hope to write soon regarding adults living with congenital heart defects.

Comments

RSS for comments on this Hub

Deone  says:
3 months ago

Very well written,Cari..Sometimes I look back on that time and wonder how we made it through. Dad and I were so young and you had so much to endure..

Specialk3749  says:
3 months ago

Very educational, Cari! I have had one baby born with a heart murmur and thankfully, it went away. I do have a nephew who has down syndrom and he has heart problems. He had his first surgery when he was under a year of age. He hasn't had any problems till this past year when he started passing out from over exhaustion. They are now watching his heart closely. He is 26 years old now! I'm looking forward to reading your hub about adults.

breakfastpop profile image

breakfastpop  says:
3 months ago

Dear Cari Jean,

Very well-written informative hub. I am so sorry you had to suffer through this.

OTmommy profile image

OTmommy  says:
3 months ago

Very informative! I am an occupational therapist working with infants and toddlers with special needs. Many of my clients have heart defects. Another symptom I often see is babies with feeding problems who can't get that suck-swallow-breathe pattern down, so they either guzzle the bottle or breast, or only drink small amounts. This eventually leads to poor weight gain. Many of the babies I work with are waiting to have heart surgery until they gain a certain amount of weight and reach a certain age. The ironic thing is because of the heart defect, they aren't good feeders and are sometimes diagnosed with failure to thrive.

Cari Jean profile image

Cari Jean  says:
3 months ago

Hey Mom! I wonder too how you and dad did it, being so young and far away from necessary medical care. While some things I have gone through with my daughter have been difficult, I can't imagine seeing your daughter go through three open heart surgeries as a child. I am very thankful for parents like you!

Cari Jean profile image

Cari Jean  says:
3 months ago

specialk3749 - I am really hoping your nephew is seeing a cardiologist who has experience treating adults who have congenital heart defects. It is very important. For a list of these specialized cardiologists, you can go to www.achaheart.org. Thanks for reading!

Cari Jean profile image

Cari Jean  says:
3 months ago

breakfastpop - thanks for stopping by! At one time I was confused and angry at God for allowing me to have this heart condition, but really it has helped shape me into who I am today. I believe that God can always turn what was meant for bad into something good.

Cari Jean profile image

Cari Jean  says:
3 months ago

O Tommy - thanks for reading and thanks for your comment. My daughter has CP so she has seen a pediatric occupational therapist since she was six months old. I really appreciate all the work pediatric therapists do! My heart goes out to the little babies waiting to have heart surgeries and diagnosed as failure to thrive. I pray that each of them are able to gain the necessary weight and reach the age for them to have the necessary surgery so that the quality of their lives can be improved.

Godslittlechild profile image

Godslittlechild  says:
3 months ago

You're a real survivor! Thanks for the inspiration!

Cari Jean profile image

Cari Jean  says:
3 months ago

Godslittlechild - thank you for your comment. It can only be by God's grace that I am still around! He has truly been good to me.

jacobkuttyta profile image

jacobkuttyta  says:
3 months ago

Thanks for the informative hub.

Keep posting

Cari Jean profile image

Cari Jean  says:
3 months ago

jacobkuttyta - you are welcome. Thanks for reading.

Submit a Comment

Members and Guests

Sign in or sign up and post using a hubpages account.


optional


  • No HTML is allowed in comments, but URLs will be hyperlinked
  • Comments are not for promoting your hubs or other sites

working