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Atrial Septal Defect

Congenital heart defects (also called congenital heart diseases) are structural abnormalities that are present in the heart at birth.

Atrial Septal Defect

Atrial Septal Defect

What is an atrial septal defect (ASD)?

An atrial septal defect (ASD) is a hole in the septum, or muscular wall, that separates the heart’s two upper chambers (atria). An ASD occurs when part of the atrial septum does not form properly.

What causes atrial septal defects?

About 10 percent of congenital heart problems are caused by specific genetic defects. Most congenital heart defects are likely due to maternal environmental factors combined with a genetic predisposition. Environmental factors include use of alcohol and street drugs, as well as diseases such as diabetes, lupus and rubella.

Who is affected by atrial septal defects?

Atrial septal defects account for about seven percent of all congenital heart defects, making them the third most common type. In addition, ASDs are the most common congenital defect in adults and are more common among women than men.

What are the long-term effects of atrial septal defects?

Normally, the right side of the heart pumps blood that is low in oxygen to the lungs, while the heart’s left side pumps oxygen-rich blood to the body. When there is an ASD, blood from the left and right sides mix, and the heart generally does not work at its most efficient level.

The risk of problems is greater when the defect is large (greater than 2 cm). Problems may include:

  • Right heart enlargement (leading to right heart failure)
  • Heart rhythm disturbances, including atrial fibrillation or atrial flutter, occur in 50 to 60 percent of all patients over age 40 with an ASD.
  • Stroke
  • Pulmonary hypertension (high blood pressure in the arteries that supply blood to the lungs). Blood normally flows from the left side of the heart to the right, but in patients with an ASD and severe pulmonary hypertension, the blood flow across the ASD can reverse (flow right to left). As a result, oxygen levels in the blood will decrease, leading to a condition known as Eisenmenger syndrome.
  • Leaking tricuspid and mitral valves as a result of enlargement of the heart

Types of atrial septal defects

Within the broad category of ASDs, there are several types of defects. Atrial septal defects are classified by where they occur and their size.

A secundum ASD is a hole in the middle of the atrial septum, which lets blood flow from the left chamber to the right chamber, or from the right chamber to the left chamber, depending on pressures in the atria.

A patent foramen ovale (PFO) is a "flap" that is present when the atrial septum does not close properly at birth. A PFO allows blood to flow from the right atrium to the left atrium. This type of defect generally only permits blood flow when there is more pressure inside the chest, such as straining during a bowel movement, coughing or sneezing. Learn more about PFO.

More complicated and rare types of ASDs involve different parts of the septum and also involve abnormal blood return from the lungs (sinus venosus) or heart valve abnormalities (primum ASDs).

What are the symptoms of atrial septal defect?

Although ASDs are present from birth, there are usually no associated symptoms, and the condition can go undetected until adulthood. In some patients, the defect is discovered incidentally during a chest X-ray that reveals enlargement of the right side of the heart.

By age 50, an individual with an ASD may start having symptoms such as shortness of breath, fainting, irregular heart rhythms or fatigue after mild activity or exercise.

In people with PFO, a stroke may be the first indication of the defect. More than 40 percent of people who have a stroke but do not have any other risk factors for a stroke are diagnosed with PFO.

How is an atrial septal defect diagnosed?

An assessment for an ASD may include:

How is an atrial septal defect treated?

Treatment of an ASD depends on the type and size of the defect, its effect on the heart, and the presence of any other related conditions, such as pulmonary hypertension, valve disease or coronary artery disease.

In general, when a patient has a large ASD that causes significant shunting (flow of blood through the defect) and right-sided heart enlargement, Cleveland Clinic specialists recommend correcting the defect.

The size of the defect correlates with the degree of shunting—the more shunting, the greater the risk of long-term complications such as atrial fibrillation and pulmonary hypertension. The degree of shunting is determined by echocardiography, MRI or oxygen saturations measured during catheterization. The degree of right-heart enlargement, as measured by echocardiography or MRI, usually correlates with the degree of shunting.

Atrial septal defect repair

Nonsurgical treatment

Nonsurgical, percutaneous (through the skin) repair is the preferred treatment for most secundum ASDs, but surgery may be needed to repair other types of ASDs (see Surgical Repair section below for more information). Your doctor will determine what type of repair procedure is best for you.

Two different brands of closure devices are approved by the U.S. Food and Drug Administration for percutaneous ASD closure—Amplatzer® Septal Occluder and the GORE HELEX® Septal Occluder. The closure devices differ in design, but the placement method and their function are similar.

The device is attached to a catheter, which is inserted into a vein in the groin and advanced to the heart and through the defect, guided by X-ray and intracardiac echo. As the device slowly is pushed out of the catheter, it opens up to cover each edge of the defect, sealing it closed. Over time, tissue grows over the implant and it becomes part of the heart.

Before a percutaneous closure device procedure, the patient will have a cardiac catheterization to determine the size and location of the defect. Pressures inside the heart chambers also will be measured.

For at least the first six months after the repair, the patient will need to take an anticoagulant such as aspirin, clopidogrel or warfarin (Coumadin) to prevent clots from forming on the device.

Percutaneous closure devices for atrial septal defect repair

Percutaneous Closure Devices

AMPLATZER® device used for ASD repair (Photo used with permission from W.L. Gore & Associates, Inc.)

AMPLATZER® Septal Occluder

The AMPLATZER® Septal Occluder is a transcatheter closure device used to treat ASDs. It consists of two Nitinol wire mesh discs filled with polyester fabric. It is folded into a special delivery catheter, similar to the catheter used to cross the heart defect during catheterization.

The catheter is inserted into a vein in the leg, advanced into the atrial septum and through the defect. When the catheter is in the proper position, the device slowly is pushed out of the catheter until the discs of the device sit on each side of the defect, like a sandwich. The two discs are linked together by a short connecting waist that matches the size of the defect. The discs and the waist are filled with polyester fabric to increase the device’s closing ability. Over time, heart tissue grows over the implant, and it becomes part of the heart, permanently correcting the defect.

GORE HELEX® Septal Occluder
GORE HELEX® Septal Occluder - used for ASD repair

GORE HELEX® Septal Occluder used for ASD repair (Photo used with permission from W.L. Gore & Associates, Inc.)

The GORE HELEX® Septal Occluder is a transcatheter closure device used to treat ASDs. It is a disc-like device that consists of ePTFE patch material supported by a single Nitinol wire frame. The device is folded into a special catheter and inserted into a vein in the leg. Using a guide wire, the device is advanced through the atrial septum. When the catheter is in the correct position, the device slowly is pushed out of the catheter until it covers the defect. The device bridges the septal defect. Over time, heart tissue grows over the implant, and it becomes part of the heart, permanently correcting the defect.

Surgical repair

Prior to the introduction of percutaneous techniques, surgical closure was the only treatment option for an ASD, regardless of the type of defect. Surgical repair may be needed for large secundum ASDs and other types of ASDs.

Surgical repair usually is performed using a tissue patch, preferably from the patient’s own pericardium (the membrane around the heart). Some secundum ASDs can be surgically closed with sutures alone.

Follow-up care

The patient usually returns to the cardiologist 3, 6 and 12 months after a procedure for a follow-up physical exam and echocardiogram, and once a year thereafter. After a secundum ASD is repaired, most people can return to their regular activities without any activity restrictions (other than those associated with all heart catheterizations). Patients usually take a blood thinner for six months to a year after the repair to prevent blood clots and help the healing process. Patients who have had a stroke may need to take blood thinners indefinitely, and those with other heart problems, such as coronary artery disease or pulmonary hypertension, may need to take additional medication. 

Patients who have heart surgery to repair a defect or receive a transcatheter closure device will need to take preventive antibiotics for at least six months after the repair procedure to reduce the risk of infective endocarditis. The doctor will provide specific guidelines about when to take antibiotics. According to the American Heart Association, there is not enough evidence to recommend taking preventive antibiotics for longer than six months.

How to find a doctor if you have adult congenital heart disease

Doctors vary in quality due to differences in training and experience; hospitals differ in the number of services available. The more complex your medical problem, the greater these differences in quality become and the more they matter.

Clearly, the doctor and hospital that you choose for complex, specialized medical care will have a direct impact on how well you do. To help you make this choice, read more about our Sydell and Arnold Miller Family Heart & Vascular Institute outcomes.

The Center for Adult Congenital Heart Disease in the Sydell and Arnold Miller Family Heart & Vascular Institute is a specialized center involving a multi-disciplinary group of specialists, including cardiologists, cardiac surgeons and nurses from Cardiovascular Medicine, Pediatric Cardiology, Pediatric and Congenital Heart Surgery, Cardiothoracic Surgery, Diagnostic Radiology, Pulmonary, Allergy and Critical Care Medicine, and Transplantation Center, who provide a comprehensive approach to diagnosing and treating adult congenital heart disease.

Learn more about specialized teams of doctors who treat congenital heart disease.

You may also use our MyConsult second opinion consultation using the Internet.

For younger patients with congenital heart disease:

See: About Us to learn more about the Sydell and Arnold Miller Family Heart & Vascular Institute.


If you need more information, click here to contact us, chat online with a nurse or call the Miller Family Heart and Vascular Institute Resource & Information Nurse at 216.445.9288 or toll-free at 866.289.6911. We would be happy to help you.

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Congenital heart disease is diagnosed by a murmur on a physical exam and several diagnostic tests:



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Reviewed: 07/15

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