Abstract

IntroductionOne potential mechanism of ventilator-induced lung injury (VILI) is due to shear stresses associated with alveolar instability (recruitment/derecruitment). It has been postulated that the optimal combination of tidal volume (Vt) and positive end-expiratory pressure (PEEP) stabilizes alveoli, thus diminishing recruitment/derecruitment and reducing VILI. In this study we directly visualized the effect of Vt and PEEP on alveolar mechanics and correlated alveolar stability with lung injury.MethodsIn vivo microscopy was utilized in a surfactant deactivation porcine ARDS model to observe the effects of Vt and PEEP on alveolar mechanics. In phase I (n = 3), nine combinations of Vt and PEEP were evaluated to determine which combination resulted in the most and least alveolar instability. In phase II (n = 6), data from phase I were utilized to separate animals into two groups based on the combination of Vt and PEEP that caused the most alveolar stability (high Vt [15 cc/kg] plus low PEEP [5 cmH2O]) and least alveolar stability (low Vt [6 cc/kg] and plus PEEP [20 cmH2O]). The animals were ventilated for three hours following lung injury, with in vivo alveolar stability measured and VILI assessed by lung function, blood gases, morphometrically, and by changes in inflammatory mediators.ResultsHigh Vt/low PEEP resulted in the most alveolar instability and lung injury, as indicated by lung function and morphometric analysis of lung tissue. Low Vt/high PEEP stabilized alveoli, improved oxygenation, and reduced lung injury. There were no significant differences between groups in plasma or bronchoalveolar lavage cytokines or proteases.ConclusionA ventilatory strategy employing high Vt and low PEEP causes alveolar instability, and to our knowledge this is the first study to confirm this finding by direct visualization. These studies demonstrate that low Vt and high PEEP work synergistically to stabilize alveoli, although increased PEEP is more effective at stabilizing alveoli than reduced Vt. In this animal model of ARDS, alveolar instability results in lung injury (VILI) with minimal changes in plasma and bronchoalveolar lavage cytokines and proteases. This suggests that the mechanism of lung injury in the high Vt/low PEEP group was mechanical, not inflammatory in nature.

Highlights

  • One potential mechanism of ventilator-induced lung injury (VILI) is due to shear stresses associated with alveolar instability

  • A ventilatory strategy employing high Vt and low positive end-expiratory pressure (PEEP) causes alveolar instability, and to our knowledge this is the first study to confirm this finding by direct visualization

  • These studies demonstrate that low Vt and high PEEP work synergistically to stabilize alveoli, increased PEEP is more effective at stabilizing alveoli than reduced Vt

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Summary

Introduction

One potential mechanism of ventilator-induced lung injury (VILI) is due to shear stresses associated with alveolar instability (recruitment/derecruitment). Acute lung injury and its more severe manifestation, acute respiratory distress syndrome (ARDS), continue to represent significant clinical challenges with daunting mortality rates of up to 60% [1]. Treatment in this patient population remains largely supportive, with mechanical ventilation until the acute insult subsides. ARDS = acute respiratory distress syndrome; BAL = bronchoalveolar lavage; HPF = high-power field; I-ED = dynamic change in alveolar area between inspiration and expiration; I-E% = I-EΔ divided by the alveolar area at end-expiration; IL = interleukin; MMP = matrix metalloproteinase; PCO2 = partial carbon dioxide tension; PEEP = positive end-expiratory pressure; TNF = tumor necrosis factor; VILI = ventilator-induced lung injury; Vt = tidal volume. We use the novel technique of in vivo microscopy to observe and measure subpleural alveoli directly and in real time during tidal ventilation in both normal and injured lung

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