Transposition of the great arteries (TGA) factsheet

Introduction

Transposition of the great arteries (TGA) is a rare, severe heart condition where the two main arteries leaving the heart are reversed. 

The heart is made up of:

  • left and right atrium – the top two chambers
  • left and right ventricle – the bottom two chambers
  • pulmonary artery – a passage that carries blood from the right ventricle to the lungs 
  • aorta – a passage that carries blood from the left ventricle to the rest of the body
  • coronary arteries – passages that carry blood into the heart.

In a normal heart, blood travels through the body in the following steps:

  1. the right ventricle pumps blood through the pulmonary artery into the lungs to get oxygen
  2. oxygen-rich blood travels back from the lungs into the left atrium, then down to the left ventricle
  3. the left ventricle pumps the oxygen-rich blood out to the rest of the body through the aorta.

In babies born with TGA, the position of the arteries is switched. This means:

  • the pulmonary artery is connected to the left ventricle, sending oxygen-rich blood back to the lungs
  • the aorta is connected to the right ventricle, sending oxygen-poor blood through the body.

When this happens, oxygen-rich blood cannot get through the body properly. 

TGA is a congenital heart condition. This means it is something your baby is born with.

TGA is life-threatening and needs to be corrected with surgery within the first few weeks of life.

 Signs and symptoms

Babies who are born with TGA may have symptoms like:

  • difficulty breathing
  • cyanosis - blue or grey colour in the skin
  • a weak pulse or heartbeat
  • heart murmur – a swishing sound in the heart
  • poor feeding and weight gain.

Diagnosis

TGA can be diagnosed:

  • during pregnancy with an ultrasound that looks at the structure of the baby’s heart
  • after your baby is born.

Symptoms of TGA can look like other conditions. A specialist doctor will look at your baby and order tests and scans to check the heart's structure and how it works.

Tests and scans can include:

  • pulse oximetry - a probe placed on your baby’s finger or toe to measure the level of oxygen in the blood
  • chest x-ray – to see the size and shape of the heart and lungs
  • electrocardiogram (ECG) – a test that records the heart's electrical activity and shows abnormal rhythms and heart muscle stress.
  • echocardiogram (echo) – a scan that uses sound waves to take a moving picture of the heart and heart valves
  • cardiac catheterisation – a thin tube is guided through a vein in the groin, up into the heart, and then used to get information about the structures inside.

Treatment

TGA must be treated with surgery within the first few weeks of a child’s life.

Treatment before surgery

Babies may need treatment in the neonatal intensive care unit (NICU) after they are born before they can have surgery.

Treatment before surgery can include:

  • extra oxygen through a machine
  • medications that help keep certain parts of the heart open, allowing the blood to mix better
  • balloon atrial septostomy - where a thin tube with a balloon is inserted through a cardiac catheter to create a hole in the heart, allowing the blood to mix better.

Arterial switch procedure

The procedure used to treat TGA is called an arterial switch. 

Generally, the arterial switch involves:

  1. switching the pulmonary artery over to the right ventricle
  2. switching the aorta to the left ventricle
  3. reattaching or moving the coronary arteries.

Your child’s surgeon may also repair any other heart issues that are found.

 Management

Long-term complications

Children who have surgery for TGA will still need life-long care under a heart specialist, known as a cardiologist.

They may be at a higher risk of heart complications, including:

  • issues with the coronary artery
  • issues with the heart muscles
  • bulges in the aorta
  • the pulmonary artery becoming narrow
  • heart failure
  • leaking from the heart valves.

Congenitally Corrected Transposition (ccTGA)

Congenitally Corrected Transposition (L-TGA) is a less common condition similar to TGA. In ccTGA, the bottom two ventricles of the heart are switched.

In ccTGA, the blood can flow properly, but the heart can develop problems with pumping over time.

Symptoms may take longer to notice, and treatment can include the repair of a ventricular septal defect (VSD).

Disclaimer

This factsheet is provided for general information only. It does not constitute health advice and should not be used to diagnose or treat any health condition.

Please consult with your doctor or other health professional to make sure this information is right for you and/or your child.

The Sydney Children’s Hospitals Network does not accept responsibility for inaccuracies or omissions, the interpretation of the information, or for success or appropriateness of any treatment described in the factsheet.

© Sydney Children’s Hospitals Network 2024


This factsheet was produced with support from John Hunter Children's Hospital.