Multicenter experience with perventricular device closure of muscular ventricular septal defects. Academic Article uri icon

Overview

abstract

  • Hybrid procedures are becoming increasingly important, especially in the management of congenital heart lesions for which there are no ideal surgical or interventional options. This report describes a multicenter experience with perventricular muscular venticular septal defect (VSD) device closure. Three groups of patients (n = 12) were identified: infants with isolated muscular VSDs (n = 2), neonates with aortic coarctation and muscular VSDs (n = 3) or patients with muscular VSDs and other complex cardiac lesions (n = 2), and patients with muscular VSDs and pulmonary artery bands (n = 5). Via a sternotomy or a subxyphoid approach, the right ventricle (RV) free wall was punctured under transesophageal echocardiography guidance. A guidewire was introduced across the largest defect. A short delivery sheath was positioned in the left ventricle cavity. An Amplatzer muscular VSD occluding device was deployed across the VSD. Cardiopulmonary bypass was needed only for repair of concomitant lesions, such as double-outlet right ventricle, aortic coarctation, or pulmonary artery band removal. No complications were encountered using this technique. Discharge echocardiograms showed either mild or no significant shunting across the ventricular septum. At a median follow-up of 12 months, all patients were asymptomatic and 2 patients had mild residual ventricular level shunts. Perventricular closure of muscular VSDs is safe and effective for a variety of patients with muscular VSDs.

authors

  • Bacha, Emile
  • Cao, Q L
  • Galantowicz, M E
  • Cheatham, J P
  • Fleishman, C E
  • Weinstein, S W
  • Becker, P A
  • Hill, S L
  • Koenig, P
  • Alboliras, E
  • Abdulla, R
  • Starr, J P
  • Hijazi, Z M

publication date

  • March 1, 2005

Research

keywords

  • Heart Defects, Congenital
  • Heart Septal Defects, Ventricular

Identity

Scopus Document Identifier

  • 27144479445

PubMed ID

  • 15868323

Additional Document Info

volume

  • 26

issue

  • 2