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Follow-up after Percutaneous Patent Ductus Arteriosus Occlusion in Lower Weight Infants
Erin Nealon1, Brian K Rivera2, Clifford L Cua1
1Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH; The Heart Center, Nationwide Children's Hospital, Columbus, OH.
Insights
Percutaneous closure of the patent ductus arteriosus (PDA) in infants under 6 kg shows improved respiratory health long-term. However, very low weight infants face higher risks, necessitating device improvements and further trials.
Area of Science:
- Pediatric Cardiology
- Interventional Cardiology
- Neonatology
Background:
- Patent ductus arteriosus (PDA) is a common condition in premature and low-birth-weight infants.
- Percutaneous closure of PDA has become an alternative to surgical ligation.
- Longer-term outcomes in infants weighing less than 6 kg are not well-described.
Purpose of the Study:
- To describe longer-term outcomes for infants weighing less than 6 kg undergoing percutaneous occlusion of the PDA.
- To examine differences in cardiopulmonary outcomes and device-related complications between very low weight (<3 kg) and low weight (3-<6 kg) infants.
Main Methods:
- Retrospective cohort study of infants <6 kg who underwent isolated percutaneous PDA closure.
- Data collected from 2003-2017 at a single, tertiary center.
- Cardiopulmonary outcomes and device-related complications were assessed using linear mixed effects models.
Main Results:
- 92 of 106 procedures were successful. Median age and weight at procedure were 3.0 months and 3.7 kg.
- Oxygenation failure (28% vs 8%) and decreased left ventricular systolic function (29% vs 5%) were higher in very low weight infants.
- Pulmonary scores improved post-procedure, suggesting better respiratory status.
Conclusions:
- Percutaneous PDA occlusion in lower weight infants may lead to long-term respiratory health improvements.
- Higher risks of complications in very low weight infants necessitate device modification.
- Clinical trials comparing percutaneous closure with alternative treatments are needed before widespread adoption.
Objectives:
To describe longer term outcomes for infants <6 kg undergoing percutaneous occlusion of the patent ductus arteriosus (PDA).
Study Design:
This was a retrospective cohort study of infants <6 kg who underwent isolated percutaneous closure of the PDA at a single, tertiary center (2003-2017). Cardiopulmonary outcomes and device-related complications (eg, left pulmonary artery obstruction) were examined for differences across weight thresholds (very low weight, <3 kg; low weight, 3-<6 kg). We assessed composite measures of respiratory status during and beyond the initial hospitalization using linear mixed effects models.
Results:
In this cohort of lower weight infants, 92 of 106 percutaneous occlusion procedures were successful. Median age and weight at procedure were 3.0 months (range, 0.5-11.1 months) and 3.7 kg (range, 1.4-5.9 kg), respectively. Among infants with pulmonary artery obstruction on initial postprocedural echocardiograms (n = 20 [22%]), obstruction persisted through hospital discharge in 3 infants. No measured variables were associated with device-related complications. Rates of oxygenation failure (28% vs 8%; P < .01) and decreased left ventricular systolic function (29% vs 5%; P < .01) were higher among very low weight than low weight infants. Pulmonary scores decreased (indicating improved respiratory status) following percutaneous PDA closure.
Conclusions:
Percutaneous PDA occlusion among lower weight infants is associated with potential longer term improvements in respiratory health. Risks of device-related complications and adverse cardiopulmonary outcomes, particularly among very low weight infants, underscore the need for continued device modification. Before widespread use, clinical trials comparing percutaneous occlusion vs alternative treatments are needed.
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