Management of Atrial Septal Defect (ASD)
Closure of an ASD is recommended for adults with right atrial and right ventricular enlargement, with or without symptoms, provided that pulmonary arterial systolic pressure is less than 50% of systemic pressure and pulmonary vascular resistance is less than one-third systemic resistance. 1
Types of ASDs and Diagnostic Approach
ASDs are classified into four main types:
- Secundum ASD (most common, 90% of cases) - defect in the central portion of atrial septum
- Primum ASD - defect in the lower portion of atrial septum
- Sinus venosus defect - defect near the entry of superior or inferior vena cava
- Coronary sinus defect - defect in the wall between coronary sinus and left atrium
Key Diagnostic Tests:
- Transthoracic echocardiography (TTE) - first-line imaging to assess:
- ASD size and location
- Right heart enlargement
- Estimated pulmonary pressures
- Qp:Qs ratio (shunt magnitude)
- Transesophageal echocardiography (TEE) - indicated when TTE is inadequate, especially for:
- Superior sinus venosus defects
- Anomalous pulmonary venous connections
- Detailed atrial septal anatomy 1
- Pulse oximetry - at rest and with exercise to detect right-to-left shunting 1
- Cardiac catheterization - when pulmonary hypertension is suspected 1
Management Algorithm
1. Indications for ASD Closure:
- Right atrial and RV enlargement (with or without symptoms) 1
- Qp:Qs ratio ≥1.5:1 1
- Paradoxical embolism 1
- Documented orthodeoxia-platypnea 1
2. Closure Method Selection:
For Secundum ASD:
- Percutaneous device closure is preferred when:
- Defect has adequate rims for device anchoring
- No associated anomalies requiring surgical repair
- Patient prefers less invasive approach
Surgical closure is indicated when:
- Sinus venosus, coronary sinus, or primum ASD (not amenable to device closure) 1
- Inadequate rims for device placement
- Large secundum ASD (>38mm)
- Need for concomitant cardiac surgery (e.g., tricuspid valve repair) 1
3. Contraindications to Closure:
- Severe irreversible pulmonary arterial hypertension with:
- PA systolic pressure >2/3 systemic
- Pulmonary vascular resistance >2/3 systemic
- Net right-to-left shunt 1
Benefits of Closure
Pooled analysis from studies shows:
- Improvement in New York Heart Association functional class
- Reduction in right ventricular systolic pressure, volumes, and dimensions 1
- Weak protective effect on adjusted mortality rate 1
- Prevention of right heart failure, exercise intolerance, and atrial arrhythmias 1
Percutaneous closure offers additional benefits:
- Shorter hospital stay
- Avoidance of sternotomy
- Lower overall complication rate (6.6% vs 31% for surgery) 2
- More rapid recovery 3
Post-Procedure Management
Medical Management:
- Atrial arrhythmias: Cardioversion after appropriate anticoagulation to restore sinus rhythm 1
- If sinus rhythm cannot be maintained: Rate control and anticoagulation 1
- After device closure: Low-dose aspirin for at least 6 months 4
Follow-up:
- Echocardiography at 24 hours, 1 month, 6 months, and annually thereafter 4
- Regular monitoring for:
- Pulmonary arterial hypertension
- Atrial arrhythmias
- RV or LV dysfunction 4
Important Considerations and Pitfalls
False-negative diagnosis: Sinus venosus defects are often missed on TTE; TEE or other advanced imaging is essential when RV volume overload is present without an obvious ASD 1
Age considerations: While early repair is preferred, ASD closure still provides benefits in older adults with right heart enlargement 1
Pulmonary hypertension assessment: Accurate evaluation of pulmonary pressures and vascular resistance is crucial before closure, as severe pulmonary hypertension is a contraindication 1
Device-related complications: Potential issues include device embolization/migration, arrhythmias, vascular access complications, and cardiac erosion/perforation 4
Small ASDs: Defects <5mm without RV volume overload may not require closure 4
By following this evidence-based approach to ASD management, clinicians can optimize outcomes related to morbidity, mortality, and quality of life for patients with this common congenital heart defect.