<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Patrier J</submitter><funding>Direction générale des armées (france)</funding><funding>Direction générale des armées</funding><pagination>300</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9527714</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The composition of the digestive microbiota may be associated with outcome and infections in patients admitted to the intensive care unit (ICU). The dominance by opportunistic pathogens (such as Enterococcus) has been associated with death. However, whether this association remains all throughout the hospitalization are lacking.&lt;h4>Methods&lt;/h4>We performed a single-center observational prospective cohort study in critically ill patients admitted with severe SARS-CoV-2 infection. Oropharyngeal and rectal swabs were collected at admission and then twice weekly until discharge or death. Quantitative cultures for opportunistic pathogens were performed on oropharyngeal and rectal swabs. The composition of the intestinal microbiota was assessed by 16S rDNA sequencing. Orophary</pubmed_abstract><journal>Critical care (London, England)</journal><pubmed_title>Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults.</pubmed_title><pmcid>PMC9527714</pmcid><funding_grant_id>project FastGeneII</funding_grant_id><pubmed_authors>Villageois-Tran K</pubmed_authors><pubmed_authors>Jaafoura S</pubmed_authors><pubmed_authors>Ruppe E</pubmed_authors><pubmed_authors>Eloy P</pubmed_authors><pubmed_authors>Mouquet H</pubmed_authors><pubmed_authors>Dorival C</pubmed_authors><pubmed_authors>Le Hingrat Q</pubmed_authors><pubmed_authors>de Montmollin E</pubmed_authors><pubmed_authors>Deplanque D</pubmed_authors><pubmed_authors>Su R</pubmed_authors><pubmed_authors>Patrier J</pubmed_authors><pubmed_authors>Goehringer F</pubmed_authors><pubmed_authors>Laouenan C</pubmed_authors><pubmed_authors>Chirouze C</pubmed_authors><pubmed_authors>Lina B</pubmed_authors><pubmed_authors>Florence AM</pubmed_authors><pubmed_authors>Paul C</pubmed_authors><pubmed_authors>Armand-Lefevre L</pubmed_authors><pubmed_authors>Beluze M</pubmed_authors><pubmed_authors>Diallo A</pubmed_authors><pubmed_authors>Petrov-Sanchez V</pubmed_authors><pubmed_authors>Gueye S</pubmed_authors><pubmed_authors>Cervantes-Gonzalez M</pubmed_authors><pubmed_authors>Rosa-Calatrava M</pubmed_authors><pubmed_authors>Le M</pubmed_authors><pubmed_authors>Levy Y</pubmed_authors><pubmed_authors>Wicky PH</pubmed_authors><pubmed_authors>Bartoli M</pubmed_authors><pubmed_authors>Timsit JF</pubmed_authors><pubmed_authors>Lafhej N</pubmed_authors><pubmed_authors>Abel L</pubmed_authors><pubmed_authors>Andrejak C</pubmed_authors><pubmed_authors>Gschwind R</pubmed_authors><pubmed_authors>Malvy D</pubmed_authors><pubmed_authors>Bouadma L</pubmed_authors><pubmed_authors>Rossignol P</pubmed_authors><pubmed_authors>Tardivon C</pubmed_authors><pubmed_authors>Couffignal C</pubmed_authors><pubmed_authors>Gigante T</pubmed_authors><pubmed_authors>Hoffmann I</pubmed_authors><pubmed_authors>Le Mestre S</pubmed_authors><pubmed_authors>Esperou H</pubmed_authors><pubmed_authors>Lingas G</pubmed_authors><pubmed_authors>da Silva FD</pubmed_authors><pubmed_authors>Houas I</pubmed_authors><pubmed_authors>Rossignol B</pubmed_authors><pubmed_authors>Sonneville R</pubmed_authors><pubmed_authors>Etienne M</pubmed_authors><pubmed_authors>Wiedemann A</pubmed_authors><pubmed_authors>Khalil A</pubmed_authors><pubmed_authors>Chair A</pubmed_authors><pubmed_authors>Debray MP</pubmed_authors><pubmed_authors>Gilg M</pubmed_authors><pubmed_authors>Behilill S</pubmed_authors><pubmed_authors>Bachelet D</pubmed_authors><pubmed_authors>Mentre F</pubmed_authors><pubmed_authors>Gaymard A</pubmed_authors><pubmed_authors>Hulot JS</pubmed_authors><pubmed_authors>Esposito-Farese M</pubmed_authors><pubmed_authors>Szychowiak P</pubmed_authors><pubmed_authors>Ruckly S</pubmed_authors><pubmed_authors>Neant N</pubmed_authors><pubmed_authors>Laribi S</pubmed_authors><pubmed_authors>Abrous A</pubmed_authors><pubmed_authors>Charpentier C</pubmed_authors><pubmed_authors>Enouf V</pubmed_authors><pubmed_authors>Marzouk M</pubmed_authors><pubmed_authors>Peytavin G</pubmed_authors><pubmed_authors>Lamara F</pubmed_authors><pubmed_authors>Picone O</pubmed_authors><pubmed_authors>French COVID Cohort Study Group</pubmed_authors><pubmed_authors>Chenard L</pubmed_authors><pubmed_authors>Descamps D</pubmed_authors><pubmed_authors>Roy C</pubmed_authors><pubmed_authors>Tubiana S</pubmed_authors><pubmed_authors>Angoulvant F</pubmed_authors><pubmed_authors>Schneider M</pubmed_authors><pubmed_authors>Letrou S</pubmed_authors><pubmed_authors>Visseaux B</pubmed_authors><pubmed_authors>Bhavsar K</pubmed_authors><pubmed_authors>Couffin-Cadiergues S</pubmed_authors><pubmed_authors>Duval X</pubmed_authors><pubmed_authors>Kafif O</pubmed_authors><pubmed_authors>Ghosn J</pubmed_authors><pubmed_authors>Guedj J</pubmed_authors><pubmed_authors>Papadopoulos A</pubmed_authors><pubmed_authors>Piquard V</pubmed_authors><pubmed_authors>Van Der Werf S</pubmed_authors><pubmed_authors>Petitjean M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Oropharyngeal and intestinal concentrations of opportunistic pathogens are independently associated with death of SARS-CoV-2 critically ill adults.</name><description>&lt;h4>Background&lt;/h4>The composition of the digestive microbiota may be associated with outcome and infections in patients admitted to the intensive care unit (ICU). The dominance by opportunistic pathogens (such as Enterococcus) has been associated with death. However, whether this association remains all throughout the hospitalization are lacking.&lt;h4>Methods&lt;/h4>We performed a single-center observational prospective cohort study in critically ill patients admitted with severe SARS-CoV-2 infection. Oropharyngeal and rectal swabs were collected at admission and then twice weekly until discharge or death. Quantitative cultures for opportunistic pathogens were performed on oropharyngeal and rectal swabs. The composition of the intestinal microbiota was assessed by 16S rDNA sequencing. Orophary</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-05-31T17:03:22.975Z</modification><creation>2024-11-07T03:09:35.027Z</creation></dates><accession>S-EPMC9527714</accession><cross_references><pubmed>36192756</pubmed><doi>10.1186/s13054-022-04164-0</doi></cross_references></HashMap>