Pediatric Artificial Lung: A Low-Resistance Pumpless Artificial Lung Alleviates an Acute Lamb Model of Increased

Fares Alghanem1, Benjamin S Bryner, Emilia M Jahangir

  • 1From the *Extracorporeal Life Support Laboratory, University of Michigan, Ann Arbor, Michigan; †Section of Transplant Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan, and ‡Section of Pediatric Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan.

ASAIO Journal (American Society for Artificial Internal Organs : 1992)
|November 19, 2016
PubMed

Insights

A novel pediatric artificial lung (PAL) effectively reduced pulmonary hypertension and improved heart function in an animal model. This device shows promise for children awaiting lung recovery or transplantation.

Area of Science:

  • Biomedical Engineering
  • Pediatric Cardiology
  • Pulmonary Medicine

Background:

  • Pediatric lung disease frequently leads to pulmonary hypertension and right heart failure.
  • A pediatric artificial lung (PAL) could offer new management strategies, bridging acute recovery or chronic transplantation.
  • Current treatment options for severe pediatric pulmonary hypertension are limited.

Purpose of the Study:

  • To evaluate the efficacy of a novel PAL in an animal model of pediatric pulmonary hypertension.
  • To assess the PAL's impact on hemodynamics, pulmonary vascular input impedance, and right ventricle efficiency.
  • To determine the PAL's potential as a bridge therapy for pediatric patients.

Main Methods:

  • Five juvenile lambs underwent PAL implantation in a pulmonary artery to left atrium configuration.
  • Pulmonary hypertension was induced via temporary occlusion of the right main pulmonary artery.
  • Hemodynamic variables, pulmonary vascular input impedance, and right ventricle efficiency were measured under baseline, disease, and disease + PAL conditions.

Main Results:

  • The disease model successfully replicated pulmonary hypertension, altering hemodynamic variables.
  • PAL attachment significantly improved pulmonary artery pressure (p = 0.018) and cardiac output (p = 0.050).
  • The PAL also reduced pulmonary vascular input impedance (Z.0 p = 0.028; Z.1 p = 0.058) and enhanced right ventricle efficiency (p = 0.001).

Conclusions:

  • This novel, low-resistance PAL effectively alleviates pulmonary hypertension in an acute animal model.
  • The PAL demonstrated significant improvements in key hemodynamic parameters and cardiac function.
  • The findings suggest the PAL holds potential as a bridge-to-transplant or bridge-to-recovery therapy for pediatric pulmonary hypertension.