LUNG EDEMA CAUSED BY HIGH PEAK INSPIRATORY PRESSURES IN DOGS - ROLE OF INCREASED MICROVASCULAR FILTRATION PRESSURE AND PERMEABILITY

Mechanical ventilation with high peak airway pressures (Paw) has been shown to induce pulmonary edema in animal experiments, but the relative contributions of transvascular filtration pressure and microvascular permeability are unclear. Therefore, we examined the effects of positive-pressure ventilation on two groups of open-chest dogs ventilated for 30 min with a peak Paw of 21.8 ± 2.3 cm H2O (Low Paw) or 64.3 ± 3.5 cm H2O (High Paw). No hemodynamic changes were observed in the Low Paw group during ventilation, but mean pulmonary artery pressure (Ppa) increased by 9.9 cm H2O peak inspiratory Ppa by 24.6 cm H2O, and estimated mean microvascular pressure by 12.5 cm H2O during High Paw ventilation. During the same period, lung lymph flow increased by 435% in the High Paw and 35% in the Low Paw groups, and the terminal extravascular lung water/blood-free dry weight ratios were 5.65 ± 0.27 and 4.43 ± 0.13 g/g, respectively, for the two groups. Lung lymph protein clearance and minimal lymph/plasma ratios of total protein were significantly higher (p < 0.05) after 2 h of increased left atrial pressure (PLA) in the High Paw group versus the Low Paw group, which indicates a significant increase in microvascular permeability. Lymph prostacyclin concentrations in pulmonary lymph, measured as the stable metabolite 6-0-PGF(1α), was increased significantly by 70 to 150% from baseline (p < 0.05) in both groups during the periods of increased Paw and increased PLA, but it was not significantly different between the groups. Thromboxane A2, measured as thromboxane B2, was increased by 40 to 50% in the lung lymph of both groups at the end of the experiments. These studies indicated that: (1) microvascular permeability was variably increased after High Paw but not after Low Paw ventilation, (2) increased microvascular filtration pressures during High Paw ventilation contributed significantly to edema formation, and (3) hemodynamic effects and injury were mediated by the mechanical effects of High Paw rather than the release of cyclooxygenase products.