Effect of transcatheter pulmonary valve implantation on short-term right ventricular function as determined by

Nasser Moiduddin1, Kentaro Asoh, Cameron Slorach

  • 1Division of Paediatric Cardiology, The Labatt Family Heart Center, The Hospital for Sick Children, Toronto, Ontario, Canada.

Insights

Transcatheter pulmonary valve implantation (PVI) improved right ventricular (RV) function in children with congenital heart disease. This emerging therapy reduced RV pressure and improved RV strain and septal function shortly after the procedure.

Area of Science:

  • Cardiology
  • Pediatric Cardiology
  • Echocardiography

Background:

  • Transcatheter pulmonary valve implantation (PVI) is an innovative treatment for right ventricular (RV) outflow dysfunction in pediatric congenital heart disease.
  • Assessing the immediate impact of PVI on RV and left ventricular (LV) function is crucial for understanding its therapeutic benefits.

Purpose of the Study:

  • To evaluate the short-term effects of PVI on RV and LV function in children post-congenital heart surgery.
  • To investigate changes in myocardial mechanics using 2D speckle tracking echocardiography and tissue Doppler imaging.

Main Methods:

  • Utilized 2D speckle tracking echocardiography and tissue Doppler imaging to assess RV and LV function before and after PVI.
  • Measured strain and strain rate of the LV, RV free wall, and interventricular septum.
  • Recorded catheter right heart hemodynamics and pulmonary regurgitation.

Main Results:

  • PVI significantly reduced the RV to pulmonary artery pressure gradient and RV end-diastolic volume.
  • Septal systolic velocities, strain, and strain rate, along with RV free wall strain, showed significant improvement post-PVI.
  • Left ventricular function, assessed by tissue velocities, strain, and strain rate, remained unchanged.

Conclusions:

  • Transcatheter pulmonary valve implantation effectively unloads the right ventricle.
  • PVI acutely enhances right ventricular and septal myocardial function in pediatric patients with congenital heart disease.

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