Device closure of secundum atrial septal defects in infants weighing less than 8 kg

Ram N Bishnoi1, Allen D Everett, Richard E Ringel

  • 1Division of Pediatric Cardiology, Johns Hopkins University School of Medicine, 1800 Orleans street M2328, Baltimore, MD, 21287, USA, rbishno1@jhmi.edu.

Pediatric Cardiology
|April 12, 2014
PubMed

Insights

Percutaneous closure of atrial septal defects (ASDs) using Amplatzer or Gore Helex devices is safe and effective in infants under 8 kg. These transcatheter procedures lead to significant clinical improvement and are rarely complicated.

Area of Science:

  • Interventional Cardiology
  • Pediatric Cardiology
  • Medical Device Technology

Background:

  • Atrial septal defects (ASDs) in infants often require intervention for failure to thrive or significant cardiac enlargement.
  • Transcatheter closure offers a less invasive alternative to surgical repair.

Purpose of the Study:

  • To evaluate the technical success, safety, and outcomes of percutaneous ASD closure in infants weighing less than 8 kg.
  • To compare the Amplatzer septal occluder (ASO) and Gore Helex septal occluder (GHSO) in this pediatric population.

Main Methods:

  • Retrospective analysis of the Mid-Atlantic Group of Interventional Cardiology Registry.
  • Inclusion of 68 infants (< 8 kg) undergoing transcatheter ASD closure at 10 US hospitals.
  • Assessment of procedural success, complications, and clinical outcomes at follow-up.

Main Results:

  • Successful device implantation in 97.1% of infants.
  • Only five minor procedure-related complications were reported.
  • Significant clinical improvement observed, including weight gain and reduced respiratory support dependence.
  • All residual shunts closed spontaneously; six late deaths were not clearly device-related.

Conclusions:

  • Transcatheter ASD closure with ASO and GHSO is a safe and effective option for infants weighing less than 8 kg.
  • The procedures are generally successful with low complication rates.
  • Significant improvements in clinical status are achievable following device implantation.