Effect of Recombinant Surfactant Protein C–Based Surfactant on the Acute Respiratory Distress Syndrome

The acute respiratory distress syndrome (ARDS) results from a deficiency of functional surfactant in the airways. These investigators carried out a multicenter study in which patients with ARDS were treated with a recombinant human surfactant protein C–based surfactant. No clinical benefits were not...

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Bibliographic Details
Published in:The New England journal of medicine Vol. 351; no. 9; pp. 884 - 892
Main Authors: Spragg, Roger G, Lewis, James F, Walmrath, Hans-Dieter, Johannigman, Jay, Bellingan, Geoff, Laterre, Pierre-Francois, Witte, Michael C, Richards, Guy A, Rippin, Gerd, Rathgeb, Frank, Häfner, Dietrich, Taut, Friedemann J.H, Seeger, Werner
Format: Journal Article
Language:English
Published: Boston, MA Massachusetts Medical Society 26-08-2004
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Summary:The acute respiratory distress syndrome (ARDS) results from a deficiency of functional surfactant in the airways. These investigators carried out a multicenter study in which patients with ARDS were treated with a recombinant human surfactant protein C–based surfactant. No clinical benefits were noted. A multicenter study in which patients with ARDS were treated with a recombinant human surfactant protein C–based surfactant. Although exogenous surfactant is of proven benefit in the prevention and treatment of the respiratory distress syndrome in infants, 1 its value in treating patients with the acute respiratory distress syndrome (ARDS) has not been established. Whereas infants with an immature lung have a deficit in surfactant production, patients with ARDS have decreased surfactant production as well as biochemical alterations of endogenous surfactant that impair surface-tension–lowering properties and decreased surfactant function in distal airways. 2 Normally, pulmonary surfactant phospholipids, acting in concert with surfactant proteins A, B, and C, cause alveolar surface tension to reach very low values at end expiration, thus . . .
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ISSN:0028-4793
1533-4406
DOI:10.1056/NEJMoa033181