Adverse ventricular-ventricular interactions in right ventricular pressure load: Insights from pediatric pulmonary

Mieke M P Driessen1, Wei Hui2, Bart H Bijnens3

  • 1Department of Pediatric Cardiology, The Labatt Family Heart Centre, The Hospital for Sick Children, Toronto, Canada Interuniversity Cardiology Institute of the Netherlands-Netherlands Heart Institute (ICIN-NHI), Utrecht, the Netherlands.

Physiological Reports
|June 16, 2016
PubMed

Insights

Pediatric idiopathic pulmonary arterial hypertension (iPAH) shows prolonged RV mechanics and septal dyskinesia, leading to biventricular dysfunction. These adverse interactions, distinct from pulmonary stenosis (PS), impact systolic and diastolic efficiency, affecting clinical outcomes.

Area of Science:

  • Cardiology
  • Pediatric Cardiology
  • Cardiovascular Physiology

Background:

  • Right ventricular (RV) pressure overload presents differently in pediatric idiopathic pulmonary arterial hypertension (iPAH) versus pulmonary stenosis (PS).
  • While RV function is a known prognostic factor in iPAH, ventricular-ventricular interactions and left ventricular (LV) dysfunction are less understood.
  • The pathophysiology driving biventricular dysfunction in pediatric iPAH requires further elucidation.

Purpose of the Study:

  • To compare ventricular-ventricular interactions as drivers of biventricular dysfunction in pediatric iPAH versus PS.
  • To investigate the distinct pathophysiological mechanisms underlying RV pressure overload in iPAH and PS.

Main Methods:

  • Retrospective study of 18 iPAH patients, 16 PS patients, and 18 age/size-matched controls.
  • Echocardiography (M-mode and Doppler) used to measure cardiac cycle events.
  • Statistical analysis (ANOVA, ANCOVA) comparing groups, with RV systolic pressure as a covariate.

Main Results:

  • Prolonged RV free wall thickening beyond pulmonary valve closure observed in iPAH compared to PS and controls.
  • Significantly prolonged LV and RV isovolumetric relaxation times in iPAH.
  • Adverse septal kinetics (rightward early systolic, leftward late RV systolic displacement) and decreased early LV diastolic filling in iPAH.

Conclusions:

  • Prolonged RV mechanics and septal dyskinesia are associated with interventricular mechanical discoordination and reduced early LV filling in pediatric iPAH.
  • These adverse mechanics contribute to impaired systolic and diastolic biventricular efficiency in iPAH, independent of RV systolic pressure.
  • Distinct ventricular-ventricular interactions in iPAH, compared to PS, may underlie worse clinical outcomes.

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