The effect of changing pulmonary artery pressure during flushing (flus
hing pressure) on lung preservation was examined in an ex vivo rabbit
lung perfusion model, Both lungs were flushed in situ with 200 ml of a
preservation solution (extracellular fluid [ECF] type) at 8 degrees C
, at a constant flushing pressure maintained by regulating the flushin
g flow rate from 20 to 120 ml/min, In the controls, the flushing press
ure was maintained at 15 mmHg and the lungs were assessed without stor
age, In the other 5 groups (n = 7 in each group), the lungs were flush
ed at pressures of 5, 10, 15, 20, and 25 mmHg, respectively, The heart
-lung block was then harvested, and immersed in the same solution at 8
degrees C for 24 hr, After 24 hr of storage, the block was reperfused
with pooled venous blood for 10 min, and then with oxygenated blood f
or another 60 min in a closed circuit, Assessment of lung function inc
luded blood gas analysis of effluent blood, pulmonary artery pressure,
airway pressure, wet:dry weight ratio, and histologic study. At flush
ing pressures of 5, 20, and 25 mmHg, uniform and clear flushing out of
the pulmonary vascular beds was not obtained, resulting in postperfus
ion pulmonary hypofunction and a high incidence of pulmonary edema, Ho
wever, at flushing pressures of 10-15 mmHg, we succeeded in completely
flushing out the pulmonary vascular beds, and managed to preserve goo
d pulmonary function, In conclusion, we determined the optimal flushin
g pressure for rabbit lung preservation to be 10-15 mmHg.