High Inflation Pressure Pulmonary Edema: Respective Effects of High Airway Pressure, High Tidal Volume, and Positive End-expiratory Pressure

Didier Dreyfuss, P Soler, Guy Basset, Georges Saumon

American Review of Respiratory Disease · 1988 · 1.7K citations · 23 references

Concepts

TL;DR

High airway pressure pulmonary edema’s pathogenesis is unclear, with uncertain contributions from high pressure versus high tidal volume, and although PEEP reduces lung water, its impact on cellular lesions has not been documented. The study compared normal tidal volume ventilation at high airway pressure with high tidal volume ventilation at high or low airway pressure, and evaluated the effects of 10 cm H₂O PEEP on edema and lung ultrastructure in mechanically ventilated rats. Edema was quantified by extravascular lung water content and microvascular permeability assessed via lung weight and the distribution space of 125I‑labeled albumin. High‑volume ventilation produced permeability edema—especially in low‑pressure, high‑volume rats—while PEEP markedly reduced edema, preserved alveolar epithelium, and represented the first evidence of PEEP’s protective effect in this model.

Abstract

The respective roles of high pressure and high tidal volume to promote high airway pressure pulmonary edema are unclear. Positive end-expiratory pressure (PEEP) was shown to reduce lung water content in this type of edema, but its possible effects on cellular lesions were not documented. We compared the consequences of normal tidal volume ventilation in mechanically ventilated rats at a high airway pressure (HiP-LoV) with those of high tidal volume ventilation at a high (HiP-HiV) or low (LoP-HiV) airway pressure and the effects of PEEP (10 cm H2O) on both edema and lung ultrastructure. Pulmonary edema was assessed by extravascular lung water content and microvascular permeability by the drug lung weight and the distribution space of 125I-labeled albumin. HiP-LoV rat lungs were not different from those of controls (7 cm H2O peak pressure ventilation). By contrast, the lungs from the groups submitted to high volume ventilation had significant permeability type edema. This edema was more pronounced in LoP-HiV rats. It was markedly reduced by PEEP, which, in addition, preserved the normal ultrastructural aspect of the alveolar epithelium. This was in striking contrast to the diffuse alveolar damage usually encountered in this type of edema. To our knowledge, this constitutes the first example of a protective effect of PEEP during permeability edema.

References

23