What is the recommended management for adult patent ductus arteriosus (PDA)?

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Last updated: December 28, 2025View editorial policy

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Management of Adult Patent Ductus Arteriosus

Primary Treatment Approach

Transcatheter device closure is the first-line treatment for adult PDA and should be prioritized over surgical intervention whenever technically feasible. 1, 2

Diagnostic Evaluation

Before determining management, perform these critical assessments:

  • Measure oxygen saturation in both feet AND both hands to detect differential cyanosis from right-to-left shunting (lower extremities may be cyanotic while upper extremities remain pink in Eisenmenger physiology) 1
  • Perform ambulatory pulse oximetry in addition to resting measurements, as some patients with resting oxygen saturation >90% will desaturate to <90% with activity, indicating dynamic shunt reversal 1
  • Echocardiography is the key diagnostic tool to assess left atrial/LV enlargement, pulmonary artery pressure, shunt direction, and cardiac chamber dimensions 1
  • Cardiac catheterization with invasive hemodynamics is indicated when pulmonary hypertension is suspected on echocardiography to accurately measure pulmonary vascular resistance and assess vasoreactivity 1

Indications for PDA Closure

Class I Recommendations (Definite Closure Indicated)

Close the PDA if ANY of the following are present: 1

  • Left atrial or left ventricular enlargement attributable to PDA with net left-to-right shunt
  • PA systolic pressure <50% of systemic pressure AND pulmonary vascular resistance <1/3 systemic resistance
  • Prior history of endarteritis (infective endocarditis)

Class IIa/IIb Recommendations (Closure May Be Considered)

PDA closure may be considered in these scenarios: 1

  • Small asymptomatic PDA with continuous murmur (reasonable to close via catheter device) 1, 3
  • Net left-to-right shunt with PA systolic pressure ≥50% systemic OR pulmonary vascular resistance >1/3 systemic but still demonstrating left-to-right flow 1
  • Even with elevated pulmonary pressures, closure may prevent further progression of pulmonary arterial hypertension if persistent left-to-right shunting exists 1

Class III (Closure Contraindicated - HARM)

DO NOT close the PDA if: 1

  • Net right-to-left shunt (Eisenmenger physiology) with PA systolic pressure >2/3 systemic OR pulmonary vascular resistance >2/3 systemic
  • This represents irreversible pulmonary vascular disease where closure would be harmful

Treatment Modality Selection

Transcatheter Device Closure (First-Line)

Device closure should be attempted first for all suitable anatomy because: 1, 2, 3

  • Success rates exceed 95% with complete closure approaching 100% in follow-up 4
  • In adults, ductal calcification and tissue friability make surgical manipulation significantly more hazardous 1
  • Large PDAs up to 16mm can be closed with available devices (AMPLATZER, Cocoon, Cera occluders) 5, 4
  • Even off-label use of large occluders (≥16mm) shows effective and safe outcomes in adolescents and adults 5

Surgical Closure (Reserved for Specific Scenarios)

Surgery should ONLY be considered when: 1, 2, 3

  • PDA is too large for available device closure
  • Distorted ductal anatomy precludes device closure (aneurysm or endarteritis)
  • Concomitant cardiac surgery is required for other indications (e.g., coronary artery bypass grafting)
  • Critical pitfall: Consult with ACHD interventional cardiologists BEFORE selecting surgical closure for calcified PDAs 1, 2
  • Surgery must be performed by a surgeon experienced in congenital heart disease 1

Special Consideration: PDA with Severe Pulmonary Hypertension

For adults with PDA and severe pulmonary arterial hypertension:

  • Trial balloon occlusion during cardiac catheterization is essential to assess hemodynamic response 6
  • If mean pulmonary arterial pressure decreases significantly after trial occlusion AND systemic oxygen saturation remains >90%, transcatheter closure can proceed safely 6
  • If pulmonary arterial pressure increases by >10mmHg after trial occlusion OR oxygen saturation drops below 85%, closure is contraindicated 6
  • Successful closure in appropriate candidates results in sustained reduction of mean pulmonary pressure (e.g., from 77mmHg to 33mmHg) 4

Post-Closure Management

Follow-Up Schedule

  • Discharge from follow-up once complete closure is documented by transthoracic echocardiography 1, 2, 3
  • For device closure: Follow-up every 5 years is recommended due to limited long-term data on device durability 1, 2, 3
  • For small unclosed PDAs without volume overload: Routine follow-up every 3-5 years 1, 3

Endocarditis Prophylaxis

  • Discontinue antibiotic prophylaxis 6 months after complete PDA closure is documented 1, 2, 3

Critical Pitfalls to Avoid

  • Never rely solely on upper extremity oxygen saturation - always check feet and both hands to avoid missing differential cyanosis 1
  • Do not assume small PDAs are benign - even small PDAs carry risk of endarteritis and may warrant closure 1, 3, 7
  • Avoid surgical closure as first-line in adults - calcification makes surgery hazardous; attempt device closure first 1, 2
  • Do not close PDAs with established Eisenmenger physiology - this causes harm 1
  • Always perform invasive hemodynamics when pulmonary hypertension is suspected - echocardiography alone may be insufficient for decision-making 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Patent Ductus Arteriosus Closure Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

PDA Closure Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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