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Late banding operation in children with ventricular septal defect and pulmonary arterial hypertension

European Journal of Cardiology
|October 1, 1975
PubMed

Insights

Pulmonary artery banding for large ventricular septal defects with pulmonary hypertension showed limited success in reducing pulmonary vascular resistance in children. Long-term follow-up revealed minimal improvement in most patients, questioning the procedure's efficacy.

Area of Science:

  • Pediatric Cardiology
  • Cardiovascular Surgery

Background:

  • Large ventricular septal defects (VSD) can lead to pulmonary arterial hypertension (PAH).
  • Pulmonary artery banding (PAB) is a palliative surgical approach for complex congenital heart disease with PAH.

Purpose of the Study:

  • To evaluate the long-term effectiveness of pulmonary artery banding in reducing pulmonary vascular resistance (PVR) in children with large VSD and PAH.

Main Methods:

  • Retrospective analysis of 31 children (2-10 years) who underwent PAB for large VSD and PAH.
  • Recatheterization of 22 children 3-5 years post-PAB to assess pressure and resistance.
  • Analysis of oxygen breathing test results pre-PAB.

Main Results:

  • Only 8 of 22 recatheterized children showed a significant pressure decrease distal to the band.
  • Pulmonary vascular resistance decreased to near-normal levels in only 2 children.
  • No significant improvement or even an increase in PVR was observed in the majority of patients.
  • Poor correlation between pressure reduction and PVR changes was noted.
  • Preoperative oxygen breathing test predicted limited PVR reduction post-PAB in some cases.

Conclusions:

  • Pulmonary artery banding offers limited long-term benefit in reducing pulmonary vascular resistance in children with large VSD and PAH.
  • The procedure's efficacy in normalizing pulmonary hemodynamics is questionable.
  • Further investigation into alternative or adjunctive treatments is warranted.

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