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Updated: Mar 29, 2026

Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure
Published on: February 8, 2022
The Ductus Dilemma: To Close or Not to Close in the Fight Against Endocarditis/Endarteritis
Tessa A E Soede1, Gabriëlle G van Iperen1, Johannes M P J Breur1
1Center for Congenital Heart Disease Utrecht, Wilhelmina Children's Hospital, University Medical Center Utrecht, 3584 EA Utrecht, The Netherlands.
Insights
Routine closure of small patent ductus arteriosus (PDA) for infective endocarditis (IEE) prevention is not justified due to low incidence versus procedural risks. Both audible and silent PDAs pose similar IEE risks, warranting guideline reassessment.
Area of Science:
- Cardiology
- Congenital Heart Defects
- Infective Endocarditis
Background:
- Patent ductus arteriosus (PDA) is a common congenital heart defect.
- Closure of hemodynamically significant PDAs is standard, but closure of small, hemodynamically insignificant PDAs for infective endocarditis or endarteritis (IEE) prevention is controversial.
- Evidence supporting IEE prevention in small PDAs is limited.
Purpose of the Study:
- To evaluate the association between PDA characteristics and IEE.
- To assess the incidence of PDA-associated IEE in relation to percutaneous PDA closure risks.
- To inform guidelines regarding the closure of hemodynamically insignificant PDAs.
Main Methods:
- Systematic PubMed search for PDA-associated IEE case reports.
- Extraction of PDA characteristics, audibility, vegetation location, and pathogens.
- Analysis of national percutaneous PDA closure data and complication rates.
Main Results:
- Seventy-two PDA-IEE cases identified; most involved audible PDAs with turbulent flow, but silent PDAs showed similar vegetation locations and flow.
- Both audible and silent PDAs can promote IEE via similar hemodynamic mechanisms.
- 61% of 76.6 annual percutaneous PDA closures were hemodynamically insignificant; 10.1% had clinically significant complications.
Conclusions:
- Routine closure of non-hemodynamically significant PDAs for IEE prevention is not clearly justified due to low IEE incidence relative to procedural risks.
- No distinction should be made between audible and silent PDAs regarding IEE risk.
- Current guidelines for PDA closure require critical reassessment.
Background:
Patent ductus arteriosus (PDA) is a common congenital heart defect. While closure of hemodynamically significant PDAs is well established, closure of small, hemodynamically insignificant PDAs for prevention of infective endocarditis or endarteritis (IEE) remains controversial and is supported only by low-level evidence.
Methods:
A systematic PubMed search was performed in May 2025 to identify published case reports of PDA-associated IEE. Data on PDA characteristics, audibility, vegetation location, and causative pathogens were extracted. In addition, the annual national number of percutaneous PDA closures in The Netherlands was determined using data from the Dutch Society of Pediatrics. Finally, the literature was searched for the incidence of complications of percutaneous ductal closure.
Results:
Seventy-two PDA-IEE cases were identified, of which fifty-five reported PDA audibility. Most cases involved audible PDAs with high-velocity turbulent flow and vegetations at sites exposed to shear stress, particularly the main pulmonary artery. Silent PDAs demonstrated similar vegetation locations and flow characteristics, suggesting that they had comparable pathophysiology. National data showed an average of 76.6 percutaneous PDA closures annually, of which 61% were hemodynamically insignificant. Adverse events during percutaneous ductal closure occur in 23.3% of procedures and clinically significant complications are reported in 10.1%. Both audible and silent PDAs appear capable of promoting IEE through similar hemodynamic mechanisms.
Conclusions:
Given the low incidence of PDA IEE relative to procedural risks, the high number needed to treat and the associated costs, routine closure of non-hemodynamically significant PDAs solely for IEE prevention is not clearly justified, and no distinction should be made between audible and silent PDAs. The current guidelines warrant critical reassessment.
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