Current Recommendations for ASD Closure Eligible by Device Criteria
For adults with secundum ASD meeting device criteria, transcatheter closure is recommended when there is right atrial and/or RV enlargement with Qp:Qs ≥1.5:1, provided PA systolic pressure is <50% of systemic pressure and PVR is <1/3 systemic vascular resistance, regardless of symptom status. 1
Primary Indications for Device Closure
Symptomatic Patients (Class I Recommendation)
- Device closure is recommended for adults with isolated secundum ASD causing impaired functional capacity, right atrial and/or RV enlargement, and Qp:Qs ≥1.5:1 without cyanosis, when PA systolic pressure <50% systemic and PVR <1/3 systemic resistance. 1
- The goal is to reduce RV volume overload and improve exercise tolerance. 1
Asymptomatic Patients (Class IIa Recommendation)
- Device closure is reasonable in asymptomatic adults when right atrial and RV enlargement are present with Qp:Qs ≥1.5:1, meeting the same hemodynamic criteria (PA pressure <50% systemic, PVR <1/3 systemic). 1
- This prevents progression to symptomatic heart failure and atrial arrhythmias. 2
Critical Hemodynamic Thresholds
Favorable Hemodynamics (Proceed with Closure)
- PA systolic pressure <50% of systemic pressure 1
- PVR <1/3 systemic vascular resistance (<5 Wood units) 1
- Qp:Qs ≥1.5:1 with evidence of RV volume overload 1
Borderline Hemodynamics (Consider Closure with Caution - Class IIb)
- PA systolic pressure 50-67% of systemic pressure 1
- PVR 1/3 to 2/3 systemic resistance (5-10 Wood units) 1
- Requires evaluation by pulmonary hypertension specialists and may benefit from vasodilator testing or trial occlusion. 1
- Recent evidence suggests patients with anatomically large defects (>25mm) and reversible PVR may benefit from fenestrated device closure with pulmonary vasodilators. 3
Absolute Contraindications (Class III - Do Not Close)
- PA systolic pressure >2/3 systemic pressure 1
- PVR >2/3 systemic vascular resistance 1
- Net right-to-left shunt (Eisenmenger physiology) 1
- Closure in these patients causes acute RV failure and death. 4
Device-Specific Anatomic Criteria
Favorable Anatomy for Device Closure
- Secundum ASD with stretched diameter <38mm 1, 5
- Adequate rim of ≥5mm in most locations (except toward the aorta where smaller rim acceptable) 1, 6
- Device closure is the preferred method when anatomically suitable, occurring in approximately 80% of secundum ASDs. 1
Deficient Rim Considerations
- Deficiency in one rim (particularly superior anterior) does not significantly influence success rate, though repositioning may be required more frequently. 6
- Large defects (>25mm) with deficient rims may still be amenable to device closure in experienced centers. 5
Special Clinical Scenarios
Paradoxical Embolism
- Device closure should be considered for ASDs of any size when paradoxical embolism is suspected after excluding other causes. 1
Concomitant Cardiac Surgery
- Surgical closure is reasonable when another cardiac procedure is being performed and Qp:Qs ≥1.5:1 with RV enlargement, even if ASD was not the primary indication. 1
Small Defects (<5mm)
- Do not require closure unless associated with paradoxical embolism, as they do not impact natural history. 2
Defects NOT Eligible for Device Closure
The following require surgical repair rather than device closure: 1
- Sinus venosus defects
- Coronary sinus defects
- Primum ASDs
- ASDs with anomalous pulmonary venous drainage
Critical Pitfalls to Avoid
Underestimating Risk in Older Adults
- Acquired conditions (hypertension, coronary disease, valvular disease) increase left-to-right shunting over time, making previously insignificant ASDs hemodynamically relevant. 4
- Even asymptomatic patients benefit from closure at any age regarding morbidity (exercise capacity, heart failure). 1
Timing of Intervention
- Outcome is best with repair before age 25 years; surgery after this age results in reduced survival compared to age-matched controls. 2
- Nearly 25% of patients with unoperated ASDs die before age 27, and 90% by age 60. 2
Pulmonary Hypertension Assessment
- The most critical assessment is excluding severe PAH before closure. 4
- Invasive hemodynamic assessment is required when PA pressure is elevated on echocardiography. 1
Post-Procedure Monitoring
- Antiplatelet therapy (aspirin 100mg daily minimum) is required for at least 6 months. 1, 7
- Device erosion, though rare (<1%), is life-threatening and requires urgent evaluation if new chest pain or syncope develops. 7
- Pericardial effusion may develop up to several weeks post-procedure. 7
- Atrial arrhythmias occur in 15-25% of adult patients, particularly those closed after age 40. 7
Expected Outcomes
Device Closure Success Rates
- Procedural success rate is 97-100% in appropriately selected patients. 8, 9, 6
- Complete closure rate is 82% immediately, increasing to 97% at 6-24 months follow-up. 9, 6
- Serious complications occur in ≤1% of patients. 1, 2
- Early mortality is approximately 1% in the absence of PAH or major comorbidities. 1, 2