Peripheral airways injury in acute lung injury/acute respiratory distress syndrome

Manu Jain*, J. Iasha Sznajder

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

11 Scopus citations


PURPOSE OF REVIEW: Peripheral airways are less than 2 mm in diameter and comprise a relatively large cross-sectional area, which allows for slower, laminar airflow. They include both membranous bronchioles and gas exchange ducts, and have been referred to in the past as the 'quiet zone', partly because these structures were felt to contribute little to lung mechanics, and partly because they are difficult to study directly. RECENT FINDINGS: Recent studies suggest that peripheral airway dysfunction plays a significant role in acute respiratory distress syndrome, which may be exacerbated by injurious mechanical ventilation strategies. The presence of elevated airways resistance, intrinsic positive end-expiratory pressure or a lower inflection point on a pressure-volume curve of the respiratory system may indicate presence of impaired peripheral airway function. In-vitro animal and human studies have begun to elucidate the signaling mechanisms responsible for stretch and shear mediated cellular injury. SUMMARY: Understanding the pathophysiology of peripheral airway dysfunction in acute respiratory distress syndrome and mechanical ventilation continues to evolve. Greater insight into the signaling mechanisms involved in cellular injury and repair will lead to further alterations in mechanical ventilation strategies, and may lead to specific treatment options.

Original languageEnglish (US)
Pages (from-to)37-43
Number of pages7
JournalCurrent opinion in critical care
Issue number1
StatePublished - Feb 2008


  • ALI
  • ARDS
  • Lower inflection point
  • Mechanical ventilation
  • Peripheral airways

ASJC Scopus subject areas

  • Critical Care and Intensive Care Medicine


Dive into the research topics of 'Peripheral airways injury in acute lung injury/acute respiratory distress syndrome'. Together they form a unique fingerprint.

Cite this