D-Transposition of the Great Vessels :: Nationwide Children's Hospital

D-Transposition of the Great Vessels

The staff of the Adolescent and Adult Congenital Heart Disease Program at Nationwide Children's Hospital are experts in caring for patients with D-transposition of the Great Vessels (D-TGA) and other congenital heart diseases. Our program is comprised of experts with an understanding of congenital heart disease as well as patient care after surgical or specialized transcatheter therapy. A full range of diagnostic and treatment capabilities are available to our patients.

Download our D-Transposition of the Great Vessels Patient Education Handout.

 

[-] 


D-Transposition of the great vessels (d-TGA) is a congenital heart defect where the aorta and pulmonary artery are switched from their normal positions.  In the normal heart, the right ventricle pumps out to the pulmonary artery (to the lungs) and the left ventricle pumps out to the aorta (to the body). Instead, in d-TGA, the aorta comes off of the right ventricle and the pulmonary artery comes off the left ventricle. The ventricles are the pumping chambers for the heart; the left ventricle was created to handle high pressure (out to the body) and the right ventricle was created to handle lower pressure (out to the lungs). In d-TGA, the blue (low-oxygen) blood returning from the body goes right back to the body instead of going to the lungs to get oxygen (to become red blood). The red (with oxygen) blood returns from the lungs and goes right back to the lungs, instead of to the body to give the tissues oxygen.



[-] 


Early Treatment (Non-Surgical)

Shortly after birth, babies with d-TGA are blue because not enough oxygen is getting to the body. Because of this, many will undergo a cardiac catheterization (heart cath) where a small catheter (tube) is placed in a blood vessel in the groin that tunnels up into the heart. A balloon is contained on the catheter and is inflated and pulled across the wall in the upper chambers (atrial septum) of the heart to create a hole. This way, red (oxygen) blood will mix with the blue (low-oxygen) blood and improve the oxygen level in the body. However, this procedure is only temporary and later requires surgical repair.

Surgical Procedures

Up until approximately 1990, most surviving patients with d-TGA underwent a Mustard operation at around 1-2 years of age. This procedure, named after the surgeon who created it, permanently switches the red and blue blood flow by using “baffles”, typically created out of synthetic material called GorTex. These baffles direct the blood through the atria (upper collecting chambers of the heart) to the proper place. By doing so, blue (low-oxygen) blood is directed to the left ventricle and then to the lungs to pick up oxygen. The red (with oxygen) blood is directed to the right ventricle and then to the aorta and body. After this surgery, the body’s oxygen levels are expected to be normal.



[-] 


Most patients do extremely well for many years, but as they approach late teenage years and into their 20s, despite previous surgery, some may develop complications such as:

Arrhythmias

The electrical system of the heart runs from the right atrium (upper collecting chamber) and through the wall separating the ventricles (bottom pumping chambers). Due to the extensive stitching in the heart, the heart’s electrical system is often damaged, therefore patients may develop slow heart rate, fast heart rhythms, or other abnormal heart rhythms . Depending on the heart rhythm problem, these may require medication or placement of a pacemaker/and or internal cardiac defibrillator (ICD) because some abnormal heart rhythm problems may cause passing out episodes or even sudden death.

Baffle Leaks

Small leaks commonly occur over time in the Mustard baffles and cause lower oxygen in the body (blueness or cyanosis) when blue blood again mixes with the red blood and goes out to the body. They may occur in the baffles that supply blood to the lungs (systemic venous baffle) or that supplying blood to the body (pulmonary venous baffle). More concerning, is the risk for stroke or “mini-strokes” if blood clots cross this leak and enter the arteries going to the brain. For most patients, baffle leaks can be treated with procedures that do not require surgery, in the cardiac catheterization (heart cath) lab with special closure devices.

Baffle Obstruction

The baffles, that were created to switch the blood flow in the heart, are usually made from a synthetic material, called GorTex. With time, the baffles can scar which causes difficulty with blood flow (obstruction) in the heart. The most common site of obstruction is where the head and neck vein (superior vena cava) comes into the heart. Also, obstruction can occur at the point where the pulmonary veins (from the lungs) enter the heart. Baffle obstruction can cause symptoms such as shortness of breath. In most situations, baffle obstructions are diagnosed by echocardiography (heart ultrasound), however, heart MRI or catheterization may be necessary diagnostic tests to detect baffle obstruction. If the obstruction is in the systemic venous (SV) baffle, it can often be alleviated in the cardiac catheterization lab using transcatheter stent therapy with a combination of ballon angioplasty and transcatheter stent therapy. A stent is a mesh-like metal tube that is loaded into a catheter (or small tube) and is inserted into an artery in the groin. The catheter is advanced into the heart, at the area of obstruction, and a balloon is inflated causing the stent to expand and open the area of narrowing. In cases of pulmonary venous (PV) baffle obstruction, surgery is typically necessary to alleviate the narrowing.

Heart Failure

Although the heart has been repaired, it is still not normal. The right ventricle, which usually pumps blood to the lungs (low-pressure) now pumps blood to the body (high pressure). The right ventricle handles the high-pressure load fairly well for many years but, eventually begins to wear down. Eventually, it becomes dilated, boggy, and weakens. This weakening is can cause symptoms of heart failure such as shortness of breath, tiredness, chest pain, and decreased activity ability. Treatments with medicines are typically helpful and can restore some of the heart function and improve symptoms. If the function of the right ventricle continues to worsen, despite medical treatment, heart transplant is considered.

Tips for Staying Healthy

  • Maintain routine cardiac follow-up

  • Notify your cardiologist of concerning symptoms

  • Take medications as they are prescribed (including antibiotics for dental procedures, tattoos, & piercings if indicated for your heart defect)

  • Maintain a healthy weight

  • Eat a healthy diet (low-sodium, low-fat)

  • Avoid all tobacco products

  • Participate in regular aerobic exercise (walking, swimming, jogging, or biking) for at least 30 minutes, most days of the week. Patients should avoid isometric activities, or those to the point of grunting or straining (chin-ups, push-ups, heavy lifting) as these activities cause added strain to the heart

  • Avoid dietary or medication sources of stimulants (caffeine in soda or chocolate, ephedrine/pseudoephredrine-containing decongestant cold medications)

  • If you are female, it is important to plan pregnancy with your cardiologist to ensure optimal cardiac status, prior to becoming pregnant



6 Myths about Congenital Heart Disease

Video

Learn more about D-Transposition of the Great Vessels including treatment options.

Watch now »

Nationwide Children's Hospital
700 Children's Drive Columbus, Ohio 43205 614.722.2000