Congenital heart disease
In many cases, congenital heart disease is diagnosed during pregnancy. However, a diagnosis may sometimes only be confirmed after the birth.
Congenital heart disease mayinitially be suspected duringa routine ultrasound scan of the baby in the womb. Specialist ultrasound called foetal Echocardiogram will then be carried out at around 18 to 22 weeks of the pregnancy to try to confirm the exact diagnosis.
This may be also undertaken if there's a family history of congenital heart disease or where there's an increased risk. Echocardiography is a type of ultrasound scan, where high-frequency sound waves are used to create an image of the heart.
However, it's not always possible to detect heart defects, particularly mild ones, using foetal echocardiography.
The examination involves observing your baby, feeling their pulse, and listening to their heart with a stethoscope. Heart murmurs are sometimes picked up.
However, some defects don't cause any noticeable symptoms for several months or even years. You should see your GP if you or your child shows signs of the condition. Further testing can usually help to confirm or rule out a diagnosis.
Further tests that may be used to diagnose congenital heart disease are described below.
Echocardiography is often used to check the inside ofthe heart. Heart problems thatweremissed during foetal echocardiography can sometimes be detected as a child develops.
An electrocardiogram (ECG) is a test that measures the heart's electrical activity. Electrodes are placed on the skin around the heart and are connected to a computer. The computer analyses the electrical signals produced by the heart to assess how well it's beating.
A chest X-ray of the heart and lungs can be used to check whether there's an excess amount of blood in the lungs, or whether the heart is larger than normal. Both may be signs of heart disease.
Pulse oximetry is a test that measures the amount of oxygen present in the blood.
The test involves placing a special sensor on the fingertip, ear or toe that sends out light waves. A computer is connected to the sensor and measures how the light waves are absorbed.
Oxygen can affect how the light waves are absorbed, so by analysing the results, the computer can quickly determine how much oxygen is present inthe blood.
Cardiac catheterisation is a useful way of obtaining more information about exactly how the blood is being pumped through the heart.
During the procedure,asmall, flexible tubecalled a catheter is inserted into a blood vessel, usually through an artery and/or vein in the groin or arm. The catheteris moved up into the heart, guided byX-rays or sometimes an MRI scanner , and allows pressure measurements in different parts of the heart or lungs to be taken.
A coloured dye that shows up on X-rays can also be injected into the catheter. The dye can be studied as it moves through the heart, allowing the shape and function of each heart chamber, vessels and the lung to be assessed.
Cardiac catheterisation is painless, because it's carried out under a general anaesthetic or a local anaesthetic .
Being told that you or your child has a potentially complex and lifelong condition such as congenital heart disease can be a confusing and frightening experience, even ifthe condition is relatively mild.
It's natural to want to find out as much as possible about congenital heart disease, including the available treatments, and howit can affect your life.
Below is a list of charities and support groups you may find useful:
You may alsowant to find out what help isavailable for parents who care for children with complex conditions. Read tips for caring for a disabled child .
The specialist nurse at the congenital heart disease department at your hospital can point you in the direction of further information.
Congenital heart disease is a general term for a range of birth defects that affect the normal workings of the heart. The term "congenital" means the condition is present at birth.
Congenital heart disease refers to a range of possible heart defects.
Congenital heart disease can have a range of symptoms, because the condition refers to several different types of heart defect.
Congenital heart disease is caused when something disrupts the normal development of the heart. It's thought that most cases occur when something affects the heart's development during about week five of pregnancy.
In many cases, congenital heart disease is diagnosed during pregnancy. However, a diagnosis may sometimes only be confirmed after the birth.
Treatment for congenital heart disease depends on the specific defect you or your child has.
Children and adults with congenital heart disease are at an increased risk of developing further problems. Many children with congenital heart disease experience delays in their development.
As so little is known about the causes of congenital heart disease, there's no guaranteed way of avoiding having a baby with the condition.