Author:
Wildi Karin,Livingstone Samantha,Ainola Carmen,Colombo Sebastiano Maria,Heinsar Silver,Sato Noriko,Sato Kei,Bouquet Mahé,Wilson Emily,Abbate Gabriella,Passmore Margaret,Hyslop Kieran,Liu Keibun,Wang Xiaomeng,Palmieri Chiara,See Hoe Louise E.,Jung Jae-Seung,Ki Katrina,Mueller Christian,Laffey John,Pelosi Paolo,Li Bassi Gianluigi,Suen Jacky,Fraser John
Abstract
AbstractWhilst the presence of 2 subphenotypes among the heterogenous Acute Respiratory Distress Syndrome (ARDS) population is becoming clinically accepted, subphenotype-specific treatment efficacy has yet to be prospectively tested. We investigated anti-inflammatory treatment in different ARDS models in sheep, previously shown similarities to human ARDS subphenotypes, in a preclinical, randomized, blinded study. Thirty anesthetized sheep were studied up to 48 h and randomized into: (a) OA: oleic acid (n = 15) and (b) OA-LPS: oleic acid and subsequent lipopolysaccharide (n = 15) to achieve a PaO2/FiO2 ratio of < 150 mmHg. Then, animals were randomly allocated to receive treatment with methylprednisolone or erythromycin or none. Assessed outcomes were oxygenation, pulmonary mechanics, hemodynamics and survival. All animals reached ARDS. Treatment with methylprednisolone, but not erythromycin, provided the highest therapeutic benefit in Ph2 animals, leading to a significant increase in PaO2/FiO2 ratio by reducing pulmonary edema, dead space ventilation and shunt fraction. Animals treated with methylprednisolone displayed a higher survival up to 48 h than all others. In animals treated with erythromycin, there was no treatment benefit regarding assessed physiological parameters and survival in both phenotypes. Treatment with methylprednisolone improves oxygenation and survival, more so in ovine phenotype 2 which resembles the human hyperinflammatory subphenotype.
Funder
the Wesley Medical Research Foundation
Prince Charles Hospital Foundation
Publisher
Springer Science and Business Media LLC
Cited by
2 articles.
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