The atrial septal defect (ASD) is a congenital cardiac disorder in which a hole in the wall (septum) divides the upper chambers (atria) of the heart. The hole can differ in size and may close on its own or need surgery. The atrial septal defect is a congenital cardiac defect that exists at the time of birth.
There is always an opening between the upper heart chambers of a baby at the time of birth called the foramen ovale. This opening allows fetal circulation to bypass the lungs until birth. This opening is no longer required and usually closes or becomes very small within some time after birth. However, if the opening is larger than normal, it may not close after birth.
If these openings do not close, a hole is left in the atria, and called an atrial septal defect. The hole increases blood flow to the lungs and may damage the blood vessels in the lungs later on. Damage caused to the blood vessels in the lungs can lead to cardiac problems in adulthood, including pulmonary hypertension in the lungs, an arrythmia (abnormal heartbeat), stroke, and cardiac arrest.
Atrial septal defects are the third most often reported type of congenital cardiac disorder. These defects are more common in adults and found more commonly in females than males.
There are no known causes of atrial septal defects among most babies. Some babies have cardiac conditions due to genetic conditions. These types of cardiac defects may be caused due to a combination of genes and other risk factors, such as environmental conditions, food, and drugs.
Atrial septal defects types include:
The atrial septal defect occurs when the baby’s heart is in the process of developing during pregnancy. Some health conditions or medicines during pregnancy can increase a baby’s risk of ASD or other congenital cardiac defects.
The risk factors can include:
If the patient’s family history includes a congenital cardiac disorder, such as an atrial septal defect, screening by a genetic advisor can help ascertain the risk of cardiac disorders in future babies.
A minor atrial septal defect doesn’t cause any concern, as these defects often close during infancy on their own.
Larger atrial septal defects can result in serious complications, which can include:
Pulmonary high blood pressure can lead to permanent lung damage. This complication, named Eisenmenger syndrome, typically develops over time and rarely occurs in those with large atrial septal defects.
As the exact cause of the atrial septal defect is unknown, prevention is currently impossible. However, getting proper prenatal care is important. Those planning to have a baby with an atrial septal defect should work closely with their health care provider.
Their visits should target:
Treatment for an atrial septal defect (ASD) depends on the size of the hole, the patient’s age, the number of or severity of symptoms, and the presence of other cardiac conditions. Sometimes certain medicines are prescribed to help treat symptoms. Sometimes the hole is repaired via surgery. There are no specific medications that can help in repairing the hole.
If a baby is diagnosed with an atrial septal defect, the health care provider may like to monitor it for a certain period of time to see if the hole closes on its own. During this period, the health care provider will treat symptoms with medications. To prevent cardiac problems later in life, the health care provider can recommend the atrial septal defect be treated for a baby. Closure can also be recommended for an adult with severe or many symptoms. Closure of the hole may be done during heart catheterization or open-heart surgery. After completing these procedures, follow-up care will depend on the patient’s age, the size of the hole, and whether the patient has any other birth disorders.
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