Atrial septal defect is an abnormality of the upper chambers of the heart (atria) where the wall between the right and left atria does not close completely. In general the defect is a hole in the wall (septum) between the top two chambers of the heart (atria). As a group, atrial septal defects are detected in 1 child per 1500 live births. Smaller atrial septal defects may close on their own during infancy or early childhood. The health effects of holes that remain open often don’t show up until last age — usually by age 40. Many people don’t realize they have an atrial septal defect until then. Sometimes a doctor detects an atrial septal defect during a newborn exam, or during a routine exam later in life. Large and long-standing atrial septal defects can damage the heart and lungs. An who has had an undetected atrial septal defect for decades may have a shortened life span from heart failure or high blood pressure in the lungs. For children with very small ASDs, the ASD closes on its own about 90% of the time. However, most other ASDs must be closed. People with some types of heart defects, including certain rarer forms of ASD, are at greater risk of developing bacterial endocarditis, an infection of the inner surface of the heart.
The term “atrial septal defect” usually refers to holes in the atria resulting from a lack of atrial septal tissue, rather than those related to a condition called patent foramen ovale (PFO). Symptoms usually have manifested by age 30. Infants with larger atrial septal defects may have poor appetite and not grow as they should. Infants may have signs of heart failure or arrhythmias. Congenital heart defects appear to run in families and sometimes occur with other genetic problems, such as Down syndrome. A genetic counselor can predict the approximate odds that any future children will have one. An atrial septal defect allows oxygen-rich (red) blood to pass from the left atrium, through the opening in the septum, and then mix with oxygen-poor (blue) blood in the right atrium. Complete closure occurs in most individuals. In 25-30% of normal hearts, however, a probe can be passed from the right atrium to the left atrium via the foramen ovale and ostium secundum.
The person also could develop heart or blood vessel damage and be at increased risk of having a stroke or getting a heart infection. Congenital heart defects of significance occur in approximately 8 in 1000 live births. Surgical closure of the defect is recommended if the atrial septal defect is large or if symptoms occur. Anticoagulants, often called blood thinners, can help reduce the chances of developing a blood clot and having a stroke. Anti-coagulants include warfarin (Coumadin) and anti-platelet agents such as aspirin. Keep the heartbeat regular. Examples include beta-blockers (Lopressor, Inderal) and digoxin (Lanoxin). Prophylactic (preventive) antibiotics should be given prior to dental procedures to reduce the risk of developing infective endocarditis. Embolization (dislodgement of thrombi) normally go to the lung and cause pulmonary emboli. In an individual with ASD, these emboli can potentially enter the arterial system. In most cases, atrial septal defects can’t be prevented. Consider talking with a genetic counselor before getting pregnant.
Treatment for Atrial Septal Defect Tips:
1. Surgical closure of an ASD involves opening up at least one atrium and closing the defect with a patch under direct visualization.
2. Embolization (dislodgement of thrombi) normally go to the lung and cause pulmonary emboli.
3. Keep the heartbeat regular. Examples include beta-blockers (Lopressor, Inderal) and digoxin (Lanoxin).
4. Increase the strength of the heart’s contractions. Examples include digoxin (Lanoxin).
5. Decrease the amount of fluid in circulation. Doing so reduces the volume of blood that must be pumped. These medications, called diuretics, include furosemide (Lasix).
6.Prophylactic (preventive) antibiotics should be given prior to dental procedures to reduce the risk of developing infective endocarditis.
