Although one would predict that surfactant replacement therapy would b
e effective in acute respiratory distress syndrome (ARDS), a recent la
rge trial proved unsuccessful, possibly reflecting the nature of the s
urfactant used. Given the importance of the unique proteins in the act
ion of surfactant, these would seem vital components of any exogenous
surfactant. The ability to identify patients at risk of ARDS and to ch
aracterise their surfactant might allow prophylactic treatment with a
nebulised, complementary, tailor-made preparation of surfactant. Advan
ced cases might undergo bronchoscopic focal lavage to remove plasma pr
oteins and inflammatory mediators prior to focal instillation of surfa
ctant to areas of greatest need. Ventilation regimens might be adjuste
d both to minimise trauma and to conserve endogenous surfactant.