Whole-lung lavage in infants and children with pulmonary alveolar proteinosis

Karl Reiter1, Carola Schoen, Matthias Griese

  • 1Kinderklinik und Kinderpoliklinik der Universitaet Muenchen am Dr. von Haunerschen Kinderspital, Muenchen, Germany. karl.reiter@med.uni-muenchen.de

Paediatric Anaesthesia
|January 5, 2011
PubMed

Insights

A novel whole-lung lavage (WLL) technique safely adapted for pediatric patients with pulmonary alveolar proteinosis (PAP) shows promise. This modified WLL procedure offers a potential treatment option for children with this rare lung disease.

Area of Science:

  • Pediatric Pulmonology
  • Respiratory Medicine
  • Critical Care

Background:

  • Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by alveolar filling.
  • Current treatment involves therapeutic whole-lung lavage (WLL), but adult techniques require modification for pediatric patients due to airway size differences.

Purpose of the Study:

  • To describe a modified whole-lung lavage (WLL) technique suitable for treating small children with pulmonary alveolar proteinosis (PAP).

Main Methods:

  • A novel WLL technique was developed, incorporating safe single-lung ventilation.
  • An age-appropriate endotracheal tube and a balloon catheter for selective main bronchus occlusion were utilized.
  • Lavage was performed through the occluded bronchus, with effectiveness assessed by changes in oxygen requirements and adverse events.

Main Results:

  • Sixty-four WLL procedures were conducted on four pediatric patients (13 months to 7 years) with PAP.
  • Two patients demonstrated reduced oxygen dependency and improved radiological findings post-WLL.
  • Two patients did not show significant improvement; transient hypoxemia was the primary adverse effect.

Conclusions:

  • The described WLL technique, combining single-lung ventilation and balloon catheter-guided lung exclusion, can be safely and effectively applied to pediatric patients with PAP.
  • This adapted WLL method provides a viable treatment strategy for infants and young children suffering from this rare alveolar filling syndrome.
Abstract

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