Refining an acute respiratory distress syndrome animal model supported by extracorporeal membrane oxygenator: incorporating clinically relevant mechanical ventilation strategy upon development
BACKGROUND: Acute respiratory distress syndrome (ARDS) requiring veno-venous extracorporeal membrane oxygenation (VV-ECMO) is associated with high mortality. One of the primary challenges in translating preclinical findings into effective clinical treatments lies in developing animal models that accurately replicate clinical scenarios. Thus, we aimed to develop a clinically relevant novel ovine model of severe ARDS with VV-ECMO support, with the primary aim of assessing feasibility through 48-h survival, while monitoring safety and clinical relevance. METHODS: > 60 mmHg, or refractory respiratory acidosis (T0) before commencing VV-ECMO (T1), followed by a 48-h observation. The primary outcome was survival at 48 h to assess the feasibility of a novel model. All complications were also recorded, and lung tissues were obtained upon autopsy. Assessments followed the American Thoracic Society (ATS) Workshop Report 2022 recommendations, including histological assessments, alveolar-capillary barrier evaluations, and inflammatory and physiological responses. Data were analysed using the Friedman test. RESULTS: to 181 (IQR: 167-185) mmHg within 60 min, requiring additional oleic acid doses to reach injury criteria. All sheep developed hallmark features of experimental ARDS including histological evidence (filling of the alveolar space with proteinaceous alveolar fluid and debris and increasing histologic injury score), impaired alveolar-capillary barrier (elevated total protein in bronchoalveolar lavage fluid (BAL) and increased lung wet-to-dry weight ratio), inflammatory response (increase in IL6, IL-8 and neutrophil numbers in BAL), and physiologic dysfunction (e.g., impaired oxygenation, reduction in lung compliance). CONCLUSIONS: We developed a novel animal model of ARDS that closely replicates ARDS management, including lung-protective mechanical ventilation before the initiation of VV-ECMO, ensuring a prolonged 48-h survival observation without any complications. This model meets all four key features of ARDS as recommended by the latest ATS guidelines and provides an innovative platform to support clinical translation.
Authors
- Angelo Milani (ORCID: https://orcid.org/0000-0002-6572-593X)
- Jacky Y. Suen (ORCID: https://orcid.org/0000-0002-0309-2524)
- Sun Kyun Ro (ORCID: https://orcid.org/0000-0003-1472-0845)
- Hideaki Nonaka (ORCID: https://orcid.org/0000-0003-3832-8936)
- Margaret R. Passmore (ORCID: https://orcid.org/0000-0002-0859-8882)
- Silver Heinsar (ORCID: https://orcid.org/0000-0002-5004-4816)
- Shinichi Ijuin (ORCID: https://orcid.org/0000-0003-3385-1533)
- Lucia Gandini (ORCID: https://orcid.org/0000-0001-7241-3363)
- Keibun Liu (ORCID: https://orcid.org/0000-0002-6867-1420)
- Gabriella Abbate
- Carmen Ainola (ORCID: https://orcid.org/0000-0003-2930-588X)
- Molly-Rose McInerney
- Kota Hoshino
- Gianluigi Li Bassi (ORCID: https://orcid.org/0000-0002-0816-0880)
- Chiara Palmieri (ORCID: https://orcid.org/0000-0002-5791-6066)
- Kieran Hyslop (ORCID: https://orcid.org/0000-0002-6604-8758)
- Samia Farah
- Cheng Zhang (ORCID: https://orcid.org/0000-0002-5676-1779)
- Sofia Portatadino
- Nchafatso Obonyo
- Mahe Bouquet
- Gabriele Fior
- John F. Fraser
- Rachana Panduru
- Emily S. Wilson
- Kei Sato
- Caitlin McGrath
- Noriko Sato
- Joshua Paech
Institutions
- Griffith University (AU)
- Queensland University of Technology (AU)
- The University of Queensland (AU)
- International Christian University (JP)
- North Estonia Medical Centre (EE)
- Prince Charles Hospital (AU)
- University of Tartu (EE)
Publication Details
- Journal
- Intensive Care Medicine Experimental
- Published
- 2026-04-20
- DOI
- https://doi.org/10.1186/s40635-026-00892-7
- Primary Topic
- Mechanical Circulatory Support Devices
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- University of Queensland
- Senko Medical Instrument Manufacturing Company
- Prince Charles Hospital Foundation