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In many cases, congenital heart disease is diagnosed during pregnancy. However, a diagnosis may sometimes only be confirmed after the birth.
Congenital heart disease may initially be suspected during a routine ultrasound scan of the baby in the womb. Specialist ultrasound called foetal echocardiography 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.
Read more about ultrasound scans during pregnancy.
It's sometimes possible to diagnose a baby with congenital heart disease shortly after birth if some of the characteristic signs or symptoms of congenital heart disease, such as a blue tinge to the skin (cyanosis), are present.
Your baby's heart will be checked as part of the newborn physical examination. 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 of the heart. Heart problems that were missed 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 in the 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, a small, flexible tube called a catheter is inserted into a blood vessel, usually through an artery and/or vein in the groin or arm. The catheter is moved up into the heart, guided by X-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.
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 if the 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 how it can affect your life.
Below is a list of charities and support groups you may find useful:
You may also want to find out what help is available 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.