Application of anti-inflammatory treatment in two different ovine Acute Respiratory Distress Syndrome injury models: a preclinical randomized intervention study

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作者
Karin Wildi
Samantha Livingstone
Carmen Ainola
Sebastiano Maria Colombo
Silver Heinsar
Noriko Sato
Kei Sato
Mahé Bouquet
Emily Wilson
Gabriella Abbate
Margaret Passmore
Kieran Hyslop
Keibun Liu
Xiaomeng Wang
Chiara Palmieri
Louise E. See Hoe
Jae-Seung Jung
Katrina Ki
Christian Mueller
John Laffey
Paolo Pelosi
Gianluigi Li Bassi
Jacky Suen
John Fraser
机构
[1] The Prince Charles Hospital,Critical Care Research Group
[2] The University of Queensland,Cardiovascular Research Institute Basel, University Hospital Basel
[3] University of Basel,Department of Anaesthesia and Intensive Care Medicine
[4] Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico,Center for Cardiac Intensive Care, Beijing Anzhen Hospital
[5] Capital Medical University,Department of Thoracic and Cardiovascular Surgery, College of Medicine
[6] The University of Queensland,Galway University Hospitals
[7] School of Veterinary Science,Anesthesiology and Critical Care
[8] Korea University,Department of Surgical Sciences and Integrated Diagnostics
[9] University of Galway,Uniting Care Hospitals
[10] San Martino Policlinico Hospital,undefined
[11] IRCCS for Oncology and Neurosciences,undefined
[12] University of Genoa,undefined
[13] Queensland University of Technology,undefined
[14] St Andrews War Memorial and The Wesley Intensive Care Units,undefined
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Scientific Reports | / 13卷
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摘要
Whilst 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.
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