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Ultra-lung-protective ventilation and biotrauma in severe ARDS patients on veno-venous extracorporeal membrane oxygenation: a randomized controlled study
BACKGROUND: Ultra-lung-protective ventilation may be useful during veno-venous extracorporeal membrane oxygenation (vv-ECMO) for severe acute respiratory distress syndrome (ARDS) to minimize ventilator-induced lung injury and to facilitate lung recovery. The objective was to compare pulmonary and sy...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744058/ https://www.ncbi.nlm.nih.gov/pubmed/36510324 http://dx.doi.org/10.1186/s13054-022-04272-x |
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author | Guervilly, Christophe Fournier, Théotime Chommeloux, Juliette Arnaud, Laurent Pinglis, Camille Baumstarck, Karine Boucekine, Mohamed Valera, Sabine Sanz, Celine Adda, Mélanie Bobot, Mickaël Daviet, Florence Gragueb-Chatti, Ines Forel, Jean-Marie Roch, Antoine Hraiech, Sami Dignat-George, Françoise Schmidt, Matthieu Lacroix, Romaric Papazian, Laurent |
author_facet | Guervilly, Christophe Fournier, Théotime Chommeloux, Juliette Arnaud, Laurent Pinglis, Camille Baumstarck, Karine Boucekine, Mohamed Valera, Sabine Sanz, Celine Adda, Mélanie Bobot, Mickaël Daviet, Florence Gragueb-Chatti, Ines Forel, Jean-Marie Roch, Antoine Hraiech, Sami Dignat-George, Françoise Schmidt, Matthieu Lacroix, Romaric Papazian, Laurent |
author_sort | Guervilly, Christophe |
collection | PubMed |
description | BACKGROUND: Ultra-lung-protective ventilation may be useful during veno-venous extracorporeal membrane oxygenation (vv-ECMO) for severe acute respiratory distress syndrome (ARDS) to minimize ventilator-induced lung injury and to facilitate lung recovery. The objective was to compare pulmonary and systemic biotrauma evaluated by numerous biomarkers of inflammation, epithelial, endothelial injuries, and lung repair according to two ventilator strategies on vv-ECMO. METHODS: This is a prospective randomized controlled study. Patients were randomized to receive during 48 h either ultra-lung-protective ventilation combining very low tidal volume (1–2 mL/kg of predicted body weight), low respiratory rate (5–10 cycles per minute), positive expiratory transpulmonary pressure, and 16 h of prone position or lung-protective-ventilation which followed the ECMO arm of the EOLIA trial (control group). RESULTS: The primary outcome was the alveolar concentrations of interleukin-1-beta, interleukin-6, interleukin-8, surfactant protein D, and blood concentrations of serum advanced glycation end products and angiopoietin-2 48 h after randomization. Enrollment was stopped for futility after the inclusion of 39 patients. Tidal volume, respiratory rate, minute ventilation, plateau pressure, and mechanical power were significantly lower in the ultra-lung-protective group. None of the concentrations of the pre-specified biomarkers differed between the two groups 48 h after randomization. However, a trend to higher 60-day mortality was observed in the ultra-lung-protective group compared to the control group (45 vs 17%, p = 0.06). CONCLUSIONS: Despite a significant reduction in the mechanical power, ultra-lung-protective ventilation during 48 h did not reduce biotrauma in patients with vv-ECMO-supported ARDS. The impact of this ventilation strategy on clinical outcomes warrants further investigation. Trial registration Clinical trial registered with www.clinicaltrials.gov (NCT03918603). Registered 17 April 2019. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04272-x. |
format | Online Article Text |
id | pubmed-9744058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97440582022-12-13 Ultra-lung-protective ventilation and biotrauma in severe ARDS patients on veno-venous extracorporeal membrane oxygenation: a randomized controlled study Guervilly, Christophe Fournier, Théotime Chommeloux, Juliette Arnaud, Laurent Pinglis, Camille Baumstarck, Karine Boucekine, Mohamed Valera, Sabine Sanz, Celine Adda, Mélanie Bobot, Mickaël Daviet, Florence Gragueb-Chatti, Ines Forel, Jean-Marie Roch, Antoine Hraiech, Sami Dignat-George, Françoise Schmidt, Matthieu Lacroix, Romaric Papazian, Laurent Crit Care Research BACKGROUND: Ultra-lung-protective ventilation may be useful during veno-venous extracorporeal membrane oxygenation (vv-ECMO) for severe acute respiratory distress syndrome (ARDS) to minimize ventilator-induced lung injury and to facilitate lung recovery. The objective was to compare pulmonary and systemic biotrauma evaluated by numerous biomarkers of inflammation, epithelial, endothelial injuries, and lung repair according to two ventilator strategies on vv-ECMO. METHODS: This is a prospective randomized controlled study. Patients were randomized to receive during 48 h either ultra-lung-protective ventilation combining very low tidal volume (1–2 mL/kg of predicted body weight), low respiratory rate (5–10 cycles per minute), positive expiratory transpulmonary pressure, and 16 h of prone position or lung-protective-ventilation which followed the ECMO arm of the EOLIA trial (control group). RESULTS: The primary outcome was the alveolar concentrations of interleukin-1-beta, interleukin-6, interleukin-8, surfactant protein D, and blood concentrations of serum advanced glycation end products and angiopoietin-2 48 h after randomization. Enrollment was stopped for futility after the inclusion of 39 patients. Tidal volume, respiratory rate, minute ventilation, plateau pressure, and mechanical power were significantly lower in the ultra-lung-protective group. None of the concentrations of the pre-specified biomarkers differed between the two groups 48 h after randomization. However, a trend to higher 60-day mortality was observed in the ultra-lung-protective group compared to the control group (45 vs 17%, p = 0.06). CONCLUSIONS: Despite a significant reduction in the mechanical power, ultra-lung-protective ventilation during 48 h did not reduce biotrauma in patients with vv-ECMO-supported ARDS. The impact of this ventilation strategy on clinical outcomes warrants further investigation. Trial registration Clinical trial registered with www.clinicaltrials.gov (NCT03918603). Registered 17 April 2019. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04272-x. BioMed Central 2022-12-12 /pmc/articles/PMC9744058/ /pubmed/36510324 http://dx.doi.org/10.1186/s13054-022-04272-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Guervilly, Christophe Fournier, Théotime Chommeloux, Juliette Arnaud, Laurent Pinglis, Camille Baumstarck, Karine Boucekine, Mohamed Valera, Sabine Sanz, Celine Adda, Mélanie Bobot, Mickaël Daviet, Florence Gragueb-Chatti, Ines Forel, Jean-Marie Roch, Antoine Hraiech, Sami Dignat-George, Françoise Schmidt, Matthieu Lacroix, Romaric Papazian, Laurent Ultra-lung-protective ventilation and biotrauma in severe ARDS patients on veno-venous extracorporeal membrane oxygenation: a randomized controlled study |
title | Ultra-lung-protective ventilation and biotrauma in severe ARDS patients on veno-venous extracorporeal membrane oxygenation: a randomized controlled study |
title_full | Ultra-lung-protective ventilation and biotrauma in severe ARDS patients on veno-venous extracorporeal membrane oxygenation: a randomized controlled study |
title_fullStr | Ultra-lung-protective ventilation and biotrauma in severe ARDS patients on veno-venous extracorporeal membrane oxygenation: a randomized controlled study |
title_full_unstemmed | Ultra-lung-protective ventilation and biotrauma in severe ARDS patients on veno-venous extracorporeal membrane oxygenation: a randomized controlled study |
title_short | Ultra-lung-protective ventilation and biotrauma in severe ARDS patients on veno-venous extracorporeal membrane oxygenation: a randomized controlled study |
title_sort | ultra-lung-protective ventilation and biotrauma in severe ards patients on veno-venous extracorporeal membrane oxygenation: a randomized controlled study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744058/ https://www.ncbi.nlm.nih.gov/pubmed/36510324 http://dx.doi.org/10.1186/s13054-022-04272-x |
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