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Respiratory Physiology of COVID-19 and Influenza Associated Acute Respiratory Distress Syndrome

Background: There is ongoing debate whether lung physiology of COVID-19-associated acute respiratory distress syndrome (ARDS) differs from ARDS of other origin. Objective: The aim of this study was to analyze and compare how critically ill patients with COVID-19 and Influenza A or B were ventilated...

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Autores principales: Kronibus, Niklas, Seiler, Frederik, Danziger, Guy, Muellenbach, Ralf M., Reyher, Christian, Becker, André P., Kamphorst, Maren, Rixecker, Torben M., Metz, Carlos, Bals, Robert, Lepper, Philipp M., Mang, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657360/
https://www.ncbi.nlm.nih.gov/pubmed/36362465
http://dx.doi.org/10.3390/jcm11216237
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author Kronibus, Niklas
Seiler, Frederik
Danziger, Guy
Muellenbach, Ralf M.
Reyher, Christian
Becker, André P.
Kamphorst, Maren
Rixecker, Torben M.
Metz, Carlos
Bals, Robert
Lepper, Philipp M.
Mang, Sebastian
author_facet Kronibus, Niklas
Seiler, Frederik
Danziger, Guy
Muellenbach, Ralf M.
Reyher, Christian
Becker, André P.
Kamphorst, Maren
Rixecker, Torben M.
Metz, Carlos
Bals, Robert
Lepper, Philipp M.
Mang, Sebastian
author_sort Kronibus, Niklas
collection PubMed
description Background: There is ongoing debate whether lung physiology of COVID-19-associated acute respiratory distress syndrome (ARDS) differs from ARDS of other origin. Objective: The aim of this study was to analyze and compare how critically ill patients with COVID-19 and Influenza A or B were ventilated in our tertiary care center with or without extracorporeal membrane oxygenation (ECMO). We ask if acute lung failure due to COVID-19 requires different intensive care management compared to conventional ARDS. Methods: 25 patients with COVID-19-associated ARDS were matched to a cohort of 25 Influenza patients treated in our center from 2011 to 2021. Subgroup analysis addressed whether patients on ECMO received different mechanical ventilation than patients without extracorporeal support. Results: Compared to Influenza-associated ARDS, COVID-19 patients had higher ventilatory system compliance (40.7 mL/mbar [31.8–46.7 mL/mbar] vs. 31.4 mL/mbar [13.7–42.8 mL/mbar], p = 0.198), higher ventilatory ratio (1.57 [1.31–1.84] vs. 0.91 [0.44–1.38], p = 0.006) and higher minute ventilation at the time of intubation (mean minute ventilation 10.7 L/min [7.2–12.2 L/min] for COVID-19 vs. 6.0 L/min [2.5–10.1 L/min] for Influenza, p = 0.013). There were no measurable differences in P/F ratio, positive end-expiratory pressure (PEEP) and driving pressures (ΔP). Respiratory system compliance deteriorated considerably in COVID-19 patients on ECMO during 2 weeks of mechanical ventilation (C(rs), mean decrease over 2 weeks −23.87 mL/mbar ± 32.94 mL/mbar, p = 0.037) but not in ventilated Influenza patients on ECMO and less so in ventilated COVID-19 patients without ECMO. For COVID-19 patients, low driving pressures on ECMO were strongly correlated to a decline in compliance after 2 weeks (Pearson’s R 0.80, p = 0.058). Overall mortality was insignificantly lower for COVID-19 patients compared to Influenza patients (40% vs. 48%, p = 0.31). Outcome was insignificantly worse for patients requiring veno-venous ECMO in both groups (50% mortality for COVID-19 on ECMO vs. 27% without ECMO, p = 0.30/56% vs. 34% mortality for Influenza A/B with and without ECMO, p = 0.31). Conclusion: The pathophysiology of early COVID-19-associated ARDS differs from Influenza-associated acute lung failure by sustained respiratory mechanics during the early phase of ventilation. We question whether intubated COVID-19 patients on ECMO benefit from extremely low driving pressures, as this appears to accelerate derecruitment and consecutive loss of ventilatory system compliance.
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spelling pubmed-96573602022-11-15 Respiratory Physiology of COVID-19 and Influenza Associated Acute Respiratory Distress Syndrome Kronibus, Niklas Seiler, Frederik Danziger, Guy Muellenbach, Ralf M. Reyher, Christian Becker, André P. Kamphorst, Maren Rixecker, Torben M. Metz, Carlos Bals, Robert Lepper, Philipp M. Mang, Sebastian J Clin Med Article Background: There is ongoing debate whether lung physiology of COVID-19-associated acute respiratory distress syndrome (ARDS) differs from ARDS of other origin. Objective: The aim of this study was to analyze and compare how critically ill patients with COVID-19 and Influenza A or B were ventilated in our tertiary care center with or without extracorporeal membrane oxygenation (ECMO). We ask if acute lung failure due to COVID-19 requires different intensive care management compared to conventional ARDS. Methods: 25 patients with COVID-19-associated ARDS were matched to a cohort of 25 Influenza patients treated in our center from 2011 to 2021. Subgroup analysis addressed whether patients on ECMO received different mechanical ventilation than patients without extracorporeal support. Results: Compared to Influenza-associated ARDS, COVID-19 patients had higher ventilatory system compliance (40.7 mL/mbar [31.8–46.7 mL/mbar] vs. 31.4 mL/mbar [13.7–42.8 mL/mbar], p = 0.198), higher ventilatory ratio (1.57 [1.31–1.84] vs. 0.91 [0.44–1.38], p = 0.006) and higher minute ventilation at the time of intubation (mean minute ventilation 10.7 L/min [7.2–12.2 L/min] for COVID-19 vs. 6.0 L/min [2.5–10.1 L/min] for Influenza, p = 0.013). There were no measurable differences in P/F ratio, positive end-expiratory pressure (PEEP) and driving pressures (ΔP). Respiratory system compliance deteriorated considerably in COVID-19 patients on ECMO during 2 weeks of mechanical ventilation (C(rs), mean decrease over 2 weeks −23.87 mL/mbar ± 32.94 mL/mbar, p = 0.037) but not in ventilated Influenza patients on ECMO and less so in ventilated COVID-19 patients without ECMO. For COVID-19 patients, low driving pressures on ECMO were strongly correlated to a decline in compliance after 2 weeks (Pearson’s R 0.80, p = 0.058). Overall mortality was insignificantly lower for COVID-19 patients compared to Influenza patients (40% vs. 48%, p = 0.31). Outcome was insignificantly worse for patients requiring veno-venous ECMO in both groups (50% mortality for COVID-19 on ECMO vs. 27% without ECMO, p = 0.30/56% vs. 34% mortality for Influenza A/B with and without ECMO, p = 0.31). Conclusion: The pathophysiology of early COVID-19-associated ARDS differs from Influenza-associated acute lung failure by sustained respiratory mechanics during the early phase of ventilation. We question whether intubated COVID-19 patients on ECMO benefit from extremely low driving pressures, as this appears to accelerate derecruitment and consecutive loss of ventilatory system compliance. MDPI 2022-10-22 /pmc/articles/PMC9657360/ /pubmed/36362465 http://dx.doi.org/10.3390/jcm11216237 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kronibus, Niklas
Seiler, Frederik
Danziger, Guy
Muellenbach, Ralf M.
Reyher, Christian
Becker, André P.
Kamphorst, Maren
Rixecker, Torben M.
Metz, Carlos
Bals, Robert
Lepper, Philipp M.
Mang, Sebastian
Respiratory Physiology of COVID-19 and Influenza Associated Acute Respiratory Distress Syndrome
title Respiratory Physiology of COVID-19 and Influenza Associated Acute Respiratory Distress Syndrome
title_full Respiratory Physiology of COVID-19 and Influenza Associated Acute Respiratory Distress Syndrome
title_fullStr Respiratory Physiology of COVID-19 and Influenza Associated Acute Respiratory Distress Syndrome
title_full_unstemmed Respiratory Physiology of COVID-19 and Influenza Associated Acute Respiratory Distress Syndrome
title_short Respiratory Physiology of COVID-19 and Influenza Associated Acute Respiratory Distress Syndrome
title_sort respiratory physiology of covid-19 and influenza associated acute respiratory distress syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657360/
https://www.ncbi.nlm.nih.gov/pubmed/36362465
http://dx.doi.org/10.3390/jcm11216237
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