Perventricular device closure of ventricular septal defects: results in patients less than 1 year of age

Alexander Omelchenko1, Yuriy Gorbatykh1, Alexey Voitov2

  • 1Division of Congenital Heart Surgery, State Research Institute of Circulation Pathology, Novosibirsk, Russian Federation.

Insights

Perventricular device closure is a safe and effective minimally invasive treatment for infants with ventricular septal defects. This approach offers a faster recovery and better cosmetic outcomes than traditional surgery.

Area of Science:

  • Cardiovascular Surgery
  • Pediatric Cardiology
  • Medical Devices

Background:

  • Ventricular septal defects (VSDs) are common congenital heart abnormalities.
  • Conventional surgical repair often involves cardiopulmonary bypass (CBP), posing risks for infants.
  • Minimally invasive techniques are sought to improve outcomes in pediatric cardiac surgery.

Purpose of the Study:

  • To evaluate the safety and efficacy of perventricular device closure for VSDs in patients under 1 year of age.
  • To compare this technique with conventional surgical repair.
  • To assess outcomes including procedural success, complications, and recovery time.

Main Methods:

  • A cohort of 51 infants (<1 year old) with VSDs underwent perventricular device closure.
  • The procedure utilized transesophageal echocardiography (TOE) guidance without CBP.
  • VSD occlusion devices were inserted via a small sternal incision.

Main Results:

  • A high procedural success rate of 96.1% was achieved.
  • Patients experienced short intensive care unit (ICU) stays (16.5 ± 9.4 hours) and ventilation times (3.2 ± 3.5 hours).
  • No major early postoperative complications, including atrioventricular blocks or significant residual shunts, were observed.

Conclusions:

  • Perventricular device closure is a safe and highly effective option for VSDs in infants.
  • This minimally invasive approach offers advantages over conventional surgery, including faster rehabilitation and superior cosmetic results.
  • Long-term follow-up showed no residual shunts, conduction disturbances, or valve complications.
Abstract

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