Utility of Follow-Up Echocardiograms in Uncomplicated PDA Device Closures Performed After Infancy

Rachel Reo1, Erin Van Pelt1, Casey Lovelace1

  • 1Heart Center, Nationwide Children's Hospital, Columbus, OH, USA.

Insights

Lifelong echocardiograms after uncomplicated patent ductus arteriosus (PDA) device closure in children may not be necessary. Follow-up transthoracic echocardiograms (TTE) showed stable cardiac function, suggesting repeat testing might be omitted if no clinical concerns arise.

Area of Science:

  • Cardiology
  • Pediatric Cardiology
  • Medical Devices

Background:

  • Current guidelines recommend lifelong transthoracic echocardiograms (TTE) following patent ductus arteriosus (PDA) device closure.
  • The clinical utility of routine lifelong TTE follow-up after uncomplicated PDA device closure in patients treated after infancy requires evaluation.

Purpose of the Study:

  • To assess the necessity of routine lifelong follow-up TTE in patients who underwent uncomplicated PDA device closure after infancy.
  • To determine if TTE parameters remain stable or improve post-procedure in this specific patient group.

Main Methods:

  • Retrospective chart review of 189 patients who underwent PDA closure ≥ 1 year of age.
  • Exclusion criteria included other congenital heart disease or inadequate follow-up TTE.
  • Analysis focused on TTE parameters at initial, 6-month, and most recent follow-up points.

Main Results:

  • No significant changes in fractional shortening or left pulmonary artery (LPA) velocity were observed between initial and most recent TTE.
  • Left ventricular internal diastolic diameter Z-score decreased significantly, while descending aorta (DAo) peak velocity increased slightly.
  • No deaths or interventions for LPA or DAo stenosis occurred; 75 patients had repeat TTEs >1 year post-procedure without clinical management changes.

Conclusions:

  • Transthoracic echocardiogram parameters generally stabilize or improve within normal limits after uncomplicated PDA closure in patients treated after infancy.
  • Routine lifelong TTE follow-up beyond 1 year post-device placement may not be essential for this population if no clinical concerns are present.
Abstract