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Clinical phenotypes and outcomes associated with SARS-CoV-2 variant Omicron in critically ill French patients with COVID-19

Infection with SARS-CoV-2 variant Omicron is considered to be less severe than infection with variant Delta, with rarer occurrence of severe disease requiring intensive care. Little information is available on comorbid factors, clinical conditions and specific viral mutational patterns associated wi...

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Autores principales: de Prost, Nicolas, Audureau, Etienne, Heming, Nicholas, Gault, Elyanne, Pham, Tài, Chaghouri, Amal, de Montmollin, Nina, Voiriot, Guillaume, Morand-Joubert, Laurence, Joseph, Adrien, Chaix, Marie-Laure, Préau, Sébastien, Favory, Raphaël, Guigon, Aurélie, Luyt, Charles-Edouard, Burrel, Sonia, Mayaux, Julien, Marot, Stéphane, Roux, Damien, Descamps, Diane, Meireles, Sylvie, Pène, Frédéric, Rozenberg, Flore, Contou, Damien, Henry, Amandine, Gaudry, Stéphane, Brichler, Ségolène, Timsit, Jean-François, Kimmoun, Antoine, Hartard, Cédric, Jandeaux, Louise-Marie, Fafi-Kremer, Samira, Gabarre, Paul, Emery, Malo, Garcia-Sanchez, Claudio, Jochmans, Sébastien, Pitsch, Aurélia, Annane, Djillali, Azoulay, Elie, Mekontso Dessap, Armand, Rodriguez, Christophe, Pawlotsky, Jean-Michel, Fourati, Slim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555693/
https://www.ncbi.nlm.nih.gov/pubmed/36224216
http://dx.doi.org/10.1038/s41467-022-33801-z
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author de Prost, Nicolas
Audureau, Etienne
Heming, Nicholas
Gault, Elyanne
Pham, Tài
Chaghouri, Amal
de Montmollin, Nina
Voiriot, Guillaume
Morand-Joubert, Laurence
Joseph, Adrien
Chaix, Marie-Laure
Préau, Sébastien
Favory, Raphaël
Guigon, Aurélie
Luyt, Charles-Edouard
Burrel, Sonia
Mayaux, Julien
Marot, Stéphane
Roux, Damien
Descamps, Diane
Meireles, Sylvie
Pène, Frédéric
Rozenberg, Flore
Contou, Damien
Henry, Amandine
Gaudry, Stéphane
Brichler, Ségolène
Timsit, Jean-François
Kimmoun, Antoine
Hartard, Cédric
Jandeaux, Louise-Marie
Fafi-Kremer, Samira
Gabarre, Paul
Emery, Malo
Garcia-Sanchez, Claudio
Jochmans, Sébastien
Pitsch, Aurélia
Annane, Djillali
Azoulay, Elie
Mekontso Dessap, Armand
Rodriguez, Christophe
Pawlotsky, Jean-Michel
Fourati, Slim
author_facet de Prost, Nicolas
Audureau, Etienne
Heming, Nicholas
Gault, Elyanne
Pham, Tài
Chaghouri, Amal
de Montmollin, Nina
Voiriot, Guillaume
Morand-Joubert, Laurence
Joseph, Adrien
Chaix, Marie-Laure
Préau, Sébastien
Favory, Raphaël
Guigon, Aurélie
Luyt, Charles-Edouard
Burrel, Sonia
Mayaux, Julien
Marot, Stéphane
Roux, Damien
Descamps, Diane
Meireles, Sylvie
Pène, Frédéric
Rozenberg, Flore
Contou, Damien
Henry, Amandine
Gaudry, Stéphane
Brichler, Ségolène
Timsit, Jean-François
Kimmoun, Antoine
Hartard, Cédric
Jandeaux, Louise-Marie
Fafi-Kremer, Samira
Gabarre, Paul
Emery, Malo
Garcia-Sanchez, Claudio
Jochmans, Sébastien
Pitsch, Aurélia
Annane, Djillali
Azoulay, Elie
Mekontso Dessap, Armand
Rodriguez, Christophe
Pawlotsky, Jean-Michel
Fourati, Slim
author_sort de Prost, Nicolas
collection PubMed
description Infection with SARS-CoV-2 variant Omicron is considered to be less severe than infection with variant Delta, with rarer occurrence of severe disease requiring intensive care. Little information is available on comorbid factors, clinical conditions and specific viral mutational patterns associated with the severity of variant Omicron infection. In this multicenter prospective cohort study, patients consecutively admitted for severe COVID-19 in 20 intensive care units in France between December 7th 2021 and May 1st 2022 were included. Among 259 patients, we show that the clinical phenotype of patients infected with variant Omicron (n = 148) is different from that in those infected with variant Delta (n = 111). We observe no significant relationship between Delta and Omicron variant lineages/sublineages and 28-day mortality (adjusted odds ratio [95% confidence interval] = 0.68 [0.35–1.32]; p = 0.253). Among Omicron-infected patients, 43.2% are immunocompromised, most of whom have received two doses of vaccine or more (85.9%) but display a poor humoral response to vaccination. The mortality rate of immunocompromised patients infected with variant Omicron is significantly higher than that of non-immunocompromised patients (46.9% vs 26.2%; p = 0.009). In patients infected with variant Omicron, there is no association between specific sublineages (BA.1/BA.1.1 (n = 109) and BA.2 (n = 21)) or any viral genome polymorphisms/mutational profile and 28-day mortality.
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spelling pubmed-95556932022-10-13 Clinical phenotypes and outcomes associated with SARS-CoV-2 variant Omicron in critically ill French patients with COVID-19 de Prost, Nicolas Audureau, Etienne Heming, Nicholas Gault, Elyanne Pham, Tài Chaghouri, Amal de Montmollin, Nina Voiriot, Guillaume Morand-Joubert, Laurence Joseph, Adrien Chaix, Marie-Laure Préau, Sébastien Favory, Raphaël Guigon, Aurélie Luyt, Charles-Edouard Burrel, Sonia Mayaux, Julien Marot, Stéphane Roux, Damien Descamps, Diane Meireles, Sylvie Pène, Frédéric Rozenberg, Flore Contou, Damien Henry, Amandine Gaudry, Stéphane Brichler, Ségolène Timsit, Jean-François Kimmoun, Antoine Hartard, Cédric Jandeaux, Louise-Marie Fafi-Kremer, Samira Gabarre, Paul Emery, Malo Garcia-Sanchez, Claudio Jochmans, Sébastien Pitsch, Aurélia Annane, Djillali Azoulay, Elie Mekontso Dessap, Armand Rodriguez, Christophe Pawlotsky, Jean-Michel Fourati, Slim Nat Commun Article Infection with SARS-CoV-2 variant Omicron is considered to be less severe than infection with variant Delta, with rarer occurrence of severe disease requiring intensive care. Little information is available on comorbid factors, clinical conditions and specific viral mutational patterns associated with the severity of variant Omicron infection. In this multicenter prospective cohort study, patients consecutively admitted for severe COVID-19 in 20 intensive care units in France between December 7th 2021 and May 1st 2022 were included. Among 259 patients, we show that the clinical phenotype of patients infected with variant Omicron (n = 148) is different from that in those infected with variant Delta (n = 111). We observe no significant relationship between Delta and Omicron variant lineages/sublineages and 28-day mortality (adjusted odds ratio [95% confidence interval] = 0.68 [0.35–1.32]; p = 0.253). Among Omicron-infected patients, 43.2% are immunocompromised, most of whom have received two doses of vaccine or more (85.9%) but display a poor humoral response to vaccination. The mortality rate of immunocompromised patients infected with variant Omicron is significantly higher than that of non-immunocompromised patients (46.9% vs 26.2%; p = 0.009). In patients infected with variant Omicron, there is no association between specific sublineages (BA.1/BA.1.1 (n = 109) and BA.2 (n = 21)) or any viral genome polymorphisms/mutational profile and 28-day mortality. Nature Publishing Group UK 2022-10-12 /pmc/articles/PMC9555693/ /pubmed/36224216 http://dx.doi.org/10.1038/s41467-022-33801-z Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
de Prost, Nicolas
Audureau, Etienne
Heming, Nicholas
Gault, Elyanne
Pham, Tài
Chaghouri, Amal
de Montmollin, Nina
Voiriot, Guillaume
Morand-Joubert, Laurence
Joseph, Adrien
Chaix, Marie-Laure
Préau, Sébastien
Favory, Raphaël
Guigon, Aurélie
Luyt, Charles-Edouard
Burrel, Sonia
Mayaux, Julien
Marot, Stéphane
Roux, Damien
Descamps, Diane
Meireles, Sylvie
Pène, Frédéric
Rozenberg, Flore
Contou, Damien
Henry, Amandine
Gaudry, Stéphane
Brichler, Ségolène
Timsit, Jean-François
Kimmoun, Antoine
Hartard, Cédric
Jandeaux, Louise-Marie
Fafi-Kremer, Samira
Gabarre, Paul
Emery, Malo
Garcia-Sanchez, Claudio
Jochmans, Sébastien
Pitsch, Aurélia
Annane, Djillali
Azoulay, Elie
Mekontso Dessap, Armand
Rodriguez, Christophe
Pawlotsky, Jean-Michel
Fourati, Slim
Clinical phenotypes and outcomes associated with SARS-CoV-2 variant Omicron in critically ill French patients with COVID-19
title Clinical phenotypes and outcomes associated with SARS-CoV-2 variant Omicron in critically ill French patients with COVID-19
title_full Clinical phenotypes and outcomes associated with SARS-CoV-2 variant Omicron in critically ill French patients with COVID-19
title_fullStr Clinical phenotypes and outcomes associated with SARS-CoV-2 variant Omicron in critically ill French patients with COVID-19
title_full_unstemmed Clinical phenotypes and outcomes associated with SARS-CoV-2 variant Omicron in critically ill French patients with COVID-19
title_short Clinical phenotypes and outcomes associated with SARS-CoV-2 variant Omicron in critically ill French patients with COVID-19
title_sort clinical phenotypes and outcomes associated with sars-cov-2 variant omicron in critically ill french patients with covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555693/
https://www.ncbi.nlm.nih.gov/pubmed/36224216
http://dx.doi.org/10.1038/s41467-022-33801-z
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