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Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial

BACKGROUND: We sought to clarify the benefit of cytokine adsorption in patients with COVID-19 supported with venovenous extracorporeal membrane oxygenation (ECMO). METHODS: We did a single-centre, open-label, randomised, controlled trial to investigate cytokine adsorption in adult patients with seve...

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Autores principales: Supady, Alexander, Weber, Enya, Rieder, Marina, Lother, Achim, Niklaus, Tim, Zahn, Timm, Frech, Franziska, Müller, Sissi, Kuhl, Moritz, Benk, Christoph, Maier, Sven, Trummer, Georg, Flügler, Annabelle, Krüger, Kirsten, Sekandarzad, Asieb, Stachon, Peter, Zotzmann, Viviane, Bode, Christoph, Biever, Paul M, Staudacher, Dawid, Wengenmayer, Tobias, Graf, Erika, Duerschmied, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121541/
https://www.ncbi.nlm.nih.gov/pubmed/34000236
http://dx.doi.org/10.1016/S2213-2600(21)00177-6
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author Supady, Alexander
Weber, Enya
Rieder, Marina
Lother, Achim
Niklaus, Tim
Zahn, Timm
Frech, Franziska
Müller, Sissi
Kuhl, Moritz
Benk, Christoph
Maier, Sven
Trummer, Georg
Flügler, Annabelle
Krüger, Kirsten
Sekandarzad, Asieb
Stachon, Peter
Zotzmann, Viviane
Bode, Christoph
Biever, Paul M
Staudacher, Dawid
Wengenmayer, Tobias
Graf, Erika
Duerschmied, Daniel
author_facet Supady, Alexander
Weber, Enya
Rieder, Marina
Lother, Achim
Niklaus, Tim
Zahn, Timm
Frech, Franziska
Müller, Sissi
Kuhl, Moritz
Benk, Christoph
Maier, Sven
Trummer, Georg
Flügler, Annabelle
Krüger, Kirsten
Sekandarzad, Asieb
Stachon, Peter
Zotzmann, Viviane
Bode, Christoph
Biever, Paul M
Staudacher, Dawid
Wengenmayer, Tobias
Graf, Erika
Duerschmied, Daniel
author_sort Supady, Alexander
collection PubMed
description BACKGROUND: We sought to clarify the benefit of cytokine adsorption in patients with COVID-19 supported with venovenous extracorporeal membrane oxygenation (ECMO). METHODS: We did a single-centre, open-label, randomised, controlled trial to investigate cytokine adsorption in adult patients with severe COVID-19 pneumonia requiring ECMO. Patients with COVID-19 selected for ECMO at the Freiburg University Medical Center (Freiburg, Germany) were randomly assigned (1:1) to receive cytokine adsorption using the CytoSorb device or not. Randomisation was computer-generated, allocation was concealed by opaque, sequentially numbered sealed envelopes. The CytoSorb device was incorporated into the ECMO circuit before connection to the patient circuit, replaced every 24 h, and removed after 72 h. The primary endpoint was serum interleukin-6 (IL-6) concentration 72 h after initiation of ECMO analysed by intention to treat. Secondary endpoints included 30-day survival. The trial is registered with ClinicalTrials.gov (NCT04324528) and the German Clinical Trials Register (DRKS00021300) and is closed. FINDINGS: From March 29, 2020, to Dec 29, 2020, of 34 patients assessed for eligibility, 17 (50%) were treated with cytokine adsorption and 17 (50%) without. Median IL-6 decreased from 357·0 pg/mL to 98·6 pg/mL in patients randomly assigned to cytokine adsorption and from 289·0 pg/mL to 112·0 pg/mL in the control group after 72 h. One patient in each group died before 72 h. Adjusted mean log IL-6 concentrations after 72 h were 0·30 higher in the cytokine adsorption group (95% CI −0·70 to 1·30, p=0·54). Survival after 30 days was three (18%) of 17 with cytokine adsorption and 13 (76%) of 17 without cytokine adsorption (p=0·0016). INTERPRETATION: Early initiation of cytokine adsorption in patients with severe COVID-19 and venovenous ECMO did not reduce serum IL-6 and had a negative effect on survival. Cytokine adsorption should not be used during the first days of ECMO support in COVID-19. FUNDING: None.
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spelling pubmed-81215412021-05-17 Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial Supady, Alexander Weber, Enya Rieder, Marina Lother, Achim Niklaus, Tim Zahn, Timm Frech, Franziska Müller, Sissi Kuhl, Moritz Benk, Christoph Maier, Sven Trummer, Georg Flügler, Annabelle Krüger, Kirsten Sekandarzad, Asieb Stachon, Peter Zotzmann, Viviane Bode, Christoph Biever, Paul M Staudacher, Dawid Wengenmayer, Tobias Graf, Erika Duerschmied, Daniel Lancet Respir Med Articles BACKGROUND: We sought to clarify the benefit of cytokine adsorption in patients with COVID-19 supported with venovenous extracorporeal membrane oxygenation (ECMO). METHODS: We did a single-centre, open-label, randomised, controlled trial to investigate cytokine adsorption in adult patients with severe COVID-19 pneumonia requiring ECMO. Patients with COVID-19 selected for ECMO at the Freiburg University Medical Center (Freiburg, Germany) were randomly assigned (1:1) to receive cytokine adsorption using the CytoSorb device or not. Randomisation was computer-generated, allocation was concealed by opaque, sequentially numbered sealed envelopes. The CytoSorb device was incorporated into the ECMO circuit before connection to the patient circuit, replaced every 24 h, and removed after 72 h. The primary endpoint was serum interleukin-6 (IL-6) concentration 72 h after initiation of ECMO analysed by intention to treat. Secondary endpoints included 30-day survival. The trial is registered with ClinicalTrials.gov (NCT04324528) and the German Clinical Trials Register (DRKS00021300) and is closed. FINDINGS: From March 29, 2020, to Dec 29, 2020, of 34 patients assessed for eligibility, 17 (50%) were treated with cytokine adsorption and 17 (50%) without. Median IL-6 decreased from 357·0 pg/mL to 98·6 pg/mL in patients randomly assigned to cytokine adsorption and from 289·0 pg/mL to 112·0 pg/mL in the control group after 72 h. One patient in each group died before 72 h. Adjusted mean log IL-6 concentrations after 72 h were 0·30 higher in the cytokine adsorption group (95% CI −0·70 to 1·30, p=0·54). Survival after 30 days was three (18%) of 17 with cytokine adsorption and 13 (76%) of 17 without cytokine adsorption (p=0·0016). INTERPRETATION: Early initiation of cytokine adsorption in patients with severe COVID-19 and venovenous ECMO did not reduce serum IL-6 and had a negative effect on survival. Cytokine adsorption should not be used during the first days of ECMO support in COVID-19. FUNDING: None. Elsevier Ltd. 2021-07 2021-05-14 /pmc/articles/PMC8121541/ /pubmed/34000236 http://dx.doi.org/10.1016/S2213-2600(21)00177-6 Text en © 2021 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Articles
Supady, Alexander
Weber, Enya
Rieder, Marina
Lother, Achim
Niklaus, Tim
Zahn, Timm
Frech, Franziska
Müller, Sissi
Kuhl, Moritz
Benk, Christoph
Maier, Sven
Trummer, Georg
Flügler, Annabelle
Krüger, Kirsten
Sekandarzad, Asieb
Stachon, Peter
Zotzmann, Viviane
Bode, Christoph
Biever, Paul M
Staudacher, Dawid
Wengenmayer, Tobias
Graf, Erika
Duerschmied, Daniel
Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial
title Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial
title_full Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial
title_fullStr Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial
title_full_unstemmed Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial
title_short Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial
title_sort cytokine adsorption in patients with severe covid-19 pneumonia requiring extracorporeal membrane oxygenation (cycov): a single centre, open-label, randomised, controlled trial
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121541/
https://www.ncbi.nlm.nih.gov/pubmed/34000236
http://dx.doi.org/10.1016/S2213-2600(21)00177-6
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