What is the recommended treatment for an 18-year history of atrial septal defect (hole in the heart)?

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Last updated: October 13, 2025View editorial policy

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Treatment Recommendations for Atrial Septal Defect (ASD) with 18-Year History

Surgical or percutaneous closure is strongly recommended for adults with atrial septal defects causing right heart volume overload, regardless of symptom status. 1

Assessment and Indications for Intervention

  • Comprehensive evaluation should include assessment of:

    • Right ventricular (RV) size and function 1
    • Pulmonary arterial pressure 1
    • Left ventricular (LV) function 1
    • Presence of associated anomalies 1
  • Closure is indicated when there is:

    • Significant RV volume overload 1
    • Evidence of right heart enlargement 1
    • Symptoms attributable to the ASD 1
  • Pooled data analysis shows significant benefits of ASD closure including:

    • Improved New York Heart Association (NYHA) functional class (OR 13.78,95% CI 3.33-57.08) 1
    • Reduction in right ventricular systolic pressure 1
    • Improved peak oxygen consumption (VO₂) 1
    • Decreased right ventricular end-diastolic diameter (RVEDD) 1

Treatment Options

Percutaneous Device Closure

  • First-line option for secundum ASD when anatomically suitable 1
  • Advantages:
    • Less invasive procedure 2
    • Shorter hospital stay 2
    • Quicker recovery time 2
  • Requirements:
    • Adequate rim of tissue surrounding the defect (typically ≥5mm except at aortic side) 1
    • No significant associated anomalies requiring surgical repair 1

Surgical Closure

  • Indicated for:
    • ASDs not amenable to device closure (large defects, inadequate rims) 1
    • Primum ASDs, sinus venosus defects, or coronary sinus defects 2
    • When associated anomalies require surgical correction 1
    • Significant pulmonary venous anomalies 1

Timing Considerations

  • Earlier intervention is associated with better outcomes 3
  • Mortality benefit is demonstrated with ASD closure (adjusted mortality HR 0.28,95% CI 0.13-0.58) 1
  • Delaying closure increases risk of:
    • Atrial arrhythmias 4
    • Right ventricular dysfunction 4
    • Pulmonary hypertension 4
    • Reduced exercise capacity 1

Contraindications and Special Considerations

  • Eisenmenger syndrome (irreversible pulmonary hypertension with right-to-left shunting) is an absolute contraindication to ASD closure 1
  • Pulmonary vascular resistance testing is recommended in cases of suspected elevated pulmonary pressures 1
  • Female patients have higher risk of developing pulmonary vascular disease if left untreated 4

Post-Closure Management and Follow-up

  • Lifelong regular follow-up is recommended for all patients with ASD (both operated and unoperated) 1
  • Follow-up should include:
    • Assessment for residual shunts 1
    • Monitoring of AV valve function 1
    • Evaluation of ventricular size and function 1
    • Screening for pulmonary arterial pressure elevation 1
    • Detection of arrhythmias 1
  • Frequency of follow-up:
    • Every 2-3 years for repaired ASDs without significant residual abnormalities 1
    • More frequent monitoring for those with residual abnormalities 1

Outcomes and Prognosis

  • When performed before age 25, surgical closure is associated with normal life expectancy 4
  • Older adults with untreated defects have increased risk of:
    • Exercise intolerance 4
    • Atrial tachyarrhythmias 4
    • Right ventricular dysfunction 4
    • Pulmonary hypertension 4
  • Non-operated patients fare significantly worse in all hemodynamic aspects compared to those with closed defects 3

Conclusion

For an 18-year history of ASD, the evidence strongly supports closure (either percutaneous or surgical depending on anatomical considerations) to prevent long-term complications and improve quality of life, particularly when there is evidence of right heart volume overload or enlargement.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Atrial septal defects.

Lancet (London, England), 2014

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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