Symptoms
Common signs and symptoms of Atrial Septal Defect (Secundum Type) include:
When to see a doctor
If you experience severe or worsening symptoms, seek immediate medical attention. Always consult with a healthcare professional for proper diagnosis and treatment.
Causes & Risk Factors
Several factors can contribute to Atrial Septal Defect (Secundum Type).
Secundum atrial septal defects develop during the earliest weeks of pregnancy when the heart is forming.
Secundum atrial septal defects develop during the earliest weeks of pregnancy when the heart is forming. Between the fourth and sixth weeks of fetal development, a thin wall called the septum normally grows to separate the heart's right and left atria. This process involves several tissue flaps that must align and fuse properly. When the central portion of this septum, called the septum secundum, fails to develop completely or has an abnormally large opening, blood can flow between the chambers after birth.
The exact reason why this developmental process goes wrong remains largely unknown in most cases.
The exact reason why this developmental process goes wrong remains largely unknown in most cases. Genetic factors play a role, as the condition sometimes runs in families. Certain genetic syndromes, such as Holt-Oram syndrome or Down syndrome, are associated with higher rates of atrial septal defects. Environmental factors during pregnancy may also contribute, though researchers haven't identified specific triggers that consistently cause this type of heart defect.
Unlike some heart conditions that develop due to lifestyle choices or infections, secundum atrial septal defects are purely developmental.
Unlike some heart conditions that develop due to lifestyle choices or infections, secundum atrial septal defects are purely developmental. They're not caused by anything the mother did or didn't do during pregnancy. The heart simply formed differently during those crucial early weeks when most women don't even know they're pregnant. This random developmental variation affects families across all backgrounds and ethnicities.
Risk Factors
- Family history of congenital heart defects
- Genetic syndromes like Down syndrome or Holt-Oram syndrome
- Maternal diabetes during pregnancy
- Maternal alcohol consumption during pregnancy
- Maternal use of certain medications during pregnancy
- Maternal viral infections during early pregnancy
- Being born female (2:1 female predominance)
- Having other congenital anomalies
Diagnosis
How healthcare professionals diagnose Atrial Septal Defect (Secundum Type):
- 1
Diagnosing a secundum atrial septal defect often begins when a doctor hears an unusual heart sound during a routine physical exam.
Diagnosing a secundum atrial septal defect often begins when a doctor hears an unusual heart sound during a routine physical exam. This heart murmur occurs because blood flowing through the hole creates turbulence that can be detected with a stethoscope. However, not all heart murmurs indicate a problem, so additional tests are needed to confirm the diagnosis and determine the size and location of the defect.
- 2
Echocardiography serves as the primary diagnostic tool for atrial septal defects.
Echocardiography serves as the primary diagnostic tool for atrial septal defects. This painless ultrasound test creates detailed images of the heart's structure and shows how blood flows through the chambers. The test can measure the exact size of the hole, determine its precise location, and assess how much extra blood volume the right side of the heart is handling. Sometimes a special type of echocardiogram called a transesophageal echo provides even clearer images by placing the ultrasound probe in the esophagus.
- 3
Additional tests may include an electrocardiogram to check the heart's electrical activity, chest X-rays to evaluate heart size and lung blood flow, or cardiac catheterization in complex cases.
Additional tests may include an electrocardiogram to check the heart's electrical activity, chest X-rays to evaluate heart size and lung blood flow, or cardiac catheterization in complex cases. Some doctors also order exercise stress tests to see how well the heart functions during physical activity. Blood tests to check oxygen levels might be performed if there are concerns about the defect's impact on circulation.
Complications
- Most small secundum atrial septal defects cause no complications throughout life.
- However, larger defects that remain untreated can lead to several serious problems over time.
- The most common long-term complication is right heart enlargement, which occurs because the right ventricle must pump extra blood that flows through the defect.
- This extra workload can eventually lead to heart failure, typically developing in the fourth or fifth decade of life if the defect hasn't been repaired.
- Other potential complications include irregular heart rhythms, particularly atrial fibrillation, and increased risk of stroke due to blood clots that can form in the enlarged right atrium.
- Some adults develop pulmonary hypertension, a condition where blood pressure in the lung arteries becomes dangerously elevated.
- Paradoxical embolism, where blood clots bypass the lungs and travel to other parts of the body, represents a rare but serious complication.
- The encouraging news is that timely repair of significant defects prevents most of these complications entirely, and even adults who undergo closure see substantial improvements in their long-term health outlook.
Prevention
- Since secundum atrial septal defects are congenital conditions that develop during early fetal heart formation, complete prevention isn't possible.
- The developmental process that creates these defects occurs so early in pregnancy that most women don't yet know they're expecting.
- However, women planning to become pregnant can take several steps that support overall fetal heart development and reduce risks of various birth defects.
- General prenatal health measures include taking folic acid supplements before conception and during early pregnancy, avoiding alcohol and recreational drugs, managing diabetes carefully if present, and discussing all medications with healthcare providers.
- Women with family histories of congenital heart defects should consider genetic counseling to understand their risks and options for prenatal screening.
- For families with one child who has an atrial septal defect, the risk of having another affected child is slightly higher than average but still relatively low.
- Fetal echocardiography during pregnancy can sometimes detect heart defects early, allowing families to plan for specialized care at birth if needed.
- While these measures can't guarantee prevention, they represent the best current approach to supporting healthy fetal development.
Treatment decisions for secundum atrial septal defects depend primarily on the size of the hole and its impact on heart function.
Treatment decisions for secundum atrial septal defects depend primarily on the size of the hole and its impact on heart function. Small defects that cause no symptoms often require only regular monitoring with periodic echocardiograms. Many small holes actually close on their own during the first two years of life as heart tissue continues to grow and develop. Children with small, asymptomatic defects can usually participate in normal activities without restrictions.
For larger defects or those causing symptoms, closure is typically recommended to prevent long-term complications.
For larger defects or those causing symptoms, closure is typically recommended to prevent long-term complications. The preferred method today is transcatheter closure, a minimally invasive procedure performed in a cardiac catheterization lab. During this procedure, a cardiologist guides a small umbrella-like device through blood vessels to plug the hole. The device is made of materials that allow heart tissue to grow over it, creating a permanent seal. Most patients go home the next day and return to normal activities within a week.
Surgical repair becomes necessary when the defect is too large for device closure or has an unusual shape.
Surgical repair becomes necessary when the defect is too large for device closure or has an unusual shape. Open-heart surgery involves making a small incision in the chest and using a patch or stitches to close the hole. While this approach requires a longer recovery period, it has excellent success rates with very low complication rates. Most children return to full activities within 6-8 weeks after surgery.
Medications rarely cure atrial septal defects but may help manage symptoms while awaiting closure.
Medications rarely cure atrial septal defects but may help manage symptoms while awaiting closure. Diuretics can reduce fluid buildup, while medications to regulate heart rhythm might be prescribed if arrhythmias develop. Blood thinners may be recommended for adults who experience strokes related to their defect. Recent advances in device technology continue to expand treatment options, making closure possible for defects that previously required surgery.
Living With Atrial Septal Defect (Secundum Type)
Children and adults with small, unoperated secundum atrial septal defects typically live normal lives with few activity restrictions. Regular checkups with a cardiologist help monitor the defect's size and the heart's function over time. Most children can participate fully in school sports and recreational activities. Parents should watch for signs of decreased exercise tolerance or unusual fatigue, but overprotection isn't necessary for most kids with small defects.
Latest Medical Developments
Latest medical developments are being researched.
Frequently Asked Questions
Update History
Mar 9, 2026v1.0.0
- Published page overview and treatments by DiseaseDirectory