What are the symptoms of an atrial septal defect?

Written by Tang Li
Cardiology
Updated on September 19, 2024
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Atrial septal defect is the most common congenital heart disease in adults, accounting for 20%-30% of adult congenital heart diseases, with a higher incidence in females than males, with a male to female ratio of about 1:1.5-3. There is also a familial tendency. Apart from larger defects, children with atrial septal defects generally show no symptoms. As they age, symptoms gradually appear, with exertional dyspnea being the main symptom, followed by supraventricular arrhythmias, especially atrial flutter and fibrillation, which exacerbate the symptoms. Some patients may develop right heart failure due to excessive right ventricular volume load. In the late stages, about 15% of patients develop severe pulmonary hypertension, resulting in a right-to-left shunt and cyanosis.

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Written by Di Zhi Yong
Cardiology
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Can atrial septal defect of the patent foramen ovale type heal itself?

This disease is a congenital heart disease, and it is recommended that the patient undergo a cardiac echocardiography. If symptoms such as palpitations and chest tightness occur, and distinct murmurs can be heard in the precordial area, surgical treatment is sometimes advised. After all, an atrial septal defect can lead to certain conditions, especially in children who are prone to pediatric pneumonia or bronchitis, which can affect their growth and development. Currently, surgical treatment is the main approach. If the issue is not very serious, the defect might heal on its own as the child grows, but this possibility is relatively small. In most cases, surgery is recommended.

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Written by Tang Li
Cardiology
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Is atrial septal defect common?

Atrial septal defect accounts for about 20%-30% of all congenital heart diseases and is more common in females. Many cases are mild in children and are not discovered until adulthood. Atrial septal defects can be classified based on anatomical abnormalities into patent foramen ovale, primary atrial septal defect, and secondary atrial septal defect. A patent foramen ovale generally does not cause shunting between the two atria. A primary atrial septal defect is located at the lower part of the atrial septum, is semicircular in shape, and is often larger, frequently associated with malformation of the mitral or tricuspid valves resulting in regurgitation. A secondary atrial septal defect is situated in the middle of the atrial septum at the fossa ovalis or near the superior and inferior vena cava. The symptoms of an atrial septal defect vary with the size of the defect; minor cases may be asymptomatic, while severe cases can result in heart failure.

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Written by Li Hai Wen
Cardiology
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How severe is an atrial septal defect considered to be?

Atrial septal defect (ASD) is a relatively common congenital heart disease in clinical practice. From a medical perspective, the severity of ASD depends on whether the patient is an adult or a child. For adults with ASD, generally speaking, defects larger than 20 millimeters are considered large atrial septal defects, which are more severe. If the defect size is between 10 and 20 millimeters, it is often classified as a moderate atrial septal defect. Defects smaller than 4 millimeters are considered small atrial septal defects. Generally, small and moderate atrial septal defects are not severe. For children, an atrial septal defect larger than 10 millimeters is considered a large atrial septal defect, which is more severe. Sizes between 5 and 10 millimeters are classified as moderate atrial septal defects. Defects smaller than 5 millimeters are considered small atrial septal defects, which generally are not severe.

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Written by Tang Li
Cardiology
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Can someone with an atrial septal defect get pregnant?

Whether patients with atrial septal defects can become pregnant depends on the following factors: 1. Whether the patient normally has symptoms. 2. Whether the echocardiography indicates heart enlargement or pulmonary hypertension. 3. The size of the atrial septal defect. 4. Whether there is a combination of arrhythmias such as atrial flutter or atrial fibrillation, and complications such as pulmonary hypertension or heart failure. For those without symptoms, and where the defect does not cause pulmonary hypertension or right heart enlargement, choosing to become pregnant is possible. Complications are not common in pregnant women with isolated atrial septal defects without pulmonary hypertension. Studies have shown that the incidence of complications in pregnant women, whether the defect is repaired or not, is relatively low. If the patient has related arrhythmias and complications, it should be closely monitored, because the cardiovascular system of the mother undergoes changes during pregnancy, leading to increased cardiac workload and a higher burden on the heart, which in turn can increase the incidence of arrhythmias. For women who are already at high risk of atrial flutter or fibrillation, this risk can increase further. Additionally, pregnant women are in an older physiological state, making it easier to form blood clots, and for those with atrial septal defects, the risk of paradoxical thrombosis increases.

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Written by Tang Li
Cardiology
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What are the symptoms of an atrial septal defect?

Atrial septal defect is the most common congenital heart disease in adults, accounting for 20%-30% of adult congenital heart diseases, with a higher incidence in females than males, with a male to female ratio of about 1:1.5-3. There is also a familial tendency. Apart from larger defects, children with atrial septal defects generally show no symptoms. As they age, symptoms gradually appear, with exertional dyspnea being the main symptom, followed by supraventricular arrhythmias, especially atrial flutter and fibrillation, which exacerbate the symptoms. Some patients may develop right heart failure due to excessive right ventricular volume load. In the late stages, about 15% of patients develop severe pulmonary hypertension, resulting in a right-to-left shunt and cyanosis.