<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>51(4)</volume><submitter>Pilgram L</submitter><funding>Charité - Universitätsmedizin Berlin</funding><pubmed_abstract>&lt;h4>Objectives&lt;/h4>The use of remdesivir (RDV) as the first drug approved for coronavirus disease 2019 (COVID-19) remains controversial. Based on the Lean European Open Survey on severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infected patients (LEOSS), we aim to contribute timing-focused complementary real-world insights to its evaluation.&lt;h4>Methods&lt;/h4>SARS-CoV-2 infected patients between January 2020 and December 2021 treated with RDV were matched 1:1 to controls considering sociodemographics, comorbidities and clinical status. Multiple imputations were used to account for missing data. Effects on fatal outcome were estimated using uni- and multivariable Cox regression models.&lt;h4>Results&lt;/h4>We included 9,687 patients. For those starting RDV administration in the complicat</pubmed_abstract><journal>Infection</journal><pagination>1033-1049</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9913009</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Use and effectiveness of remdesivir for the treatment of patients with covid-19 using data from the Lean European Open Survey on SARS-CoV-2 infected patients (LEOSS): a multicentre cohort study.</pubmed_title><pmcid>PMC9913009</pmcid><pubmed_authors>Pilgram L</pubmed_authors><pubmed_authors>de Miranda SMN</pubmed_authors><pubmed_authors>Hellwig K</pubmed_authors><pubmed_authors>Appel KS</pubmed_authors><pubmed_authors>Stecher M</pubmed_authors><pubmed_authors>Vehreschild MJGT</pubmed_authors><pubmed_authors>Vom Dahl J</pubmed_authors><pubmed_authors>Spinner CD</pubmed_authors><pubmed_authors>Hertenstein B</pubmed_authors><pubmed_authors>Hower M</pubmed_authors><pubmed_authors>Jensen BO</pubmed_authors><pubmed_authors>Wille K</pubmed_authors><pubmed_authors>Ruethrich MM</pubmed_authors><pubmed_authors>Koll CEM</pubmed_authors><pubmed_authors>Hanses F</pubmed_authors><pubmed_authors>Haselberger M</pubmed_authors><pubmed_authors>Westhoff T</pubmed_authors><pubmed_authors>Vehreschild JJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Use and effectiveness of remdesivir for the treatment of patients with covid-19 using data from the Lean European Open Survey on SARS-CoV-2 infected patients (LEOSS): a multicentre cohort study.</name><description>&lt;h4>Objectives&lt;/h4>The use of remdesivir (RDV) as the first drug approved for coronavirus disease 2019 (COVID-19) remains controversial. Based on the Lean European Open Survey on severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infected patients (LEOSS), we aim to contribute timing-focused complementary real-world insights to its evaluation.&lt;h4>Methods&lt;/h4>SARS-CoV-2 infected patients between January 2020 and December 2021 treated with RDV were matched 1:1 to controls considering sociodemographics, comorbidities and clinical status. Multiple imputations were used to account for missing data. Effects on fatal outcome were estimated using uni- and multivariable Cox regression models.&lt;h4>Results&lt;/h4>We included 9,687 patients. For those starting RDV administration in the complicat</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2025-04-04T13:08:23.454Z</modification><creation>2025-04-04T13:08:23.454Z</creation></dates><accession>S-EPMC9913009</accession><cross_references><pubmed>36763285</pubmed><doi>10.1007/s15010-023-01994-0</doi></cross_references></HashMap>