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Remdesivir plus Dexamethasone in COVID-19: A cohort study of severe patients requiring high flow oxygen therapy or non-invasive ventilation

INTRODUCTION: Remdesivir and Dexamethasone represent the cornerstone of therapy for critically ill patients with acute hypoxemic respiratory failure caused by Coronavirus Disease 2019 (COVID-19). However, clinical efficacy and safety of concomitant administration of Remdesivir and Dexamethasone (Rem...

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Autores principales: De Pascale, Gennaro, Cutuli, Salvatore Lucio, Carelli, Simone, Xhemalaj, Rikardo, Rosà, Tommaso, Bello, Giuseppe, Vargas, Joel, Cesarano, Melania, Montini, Luca, Tanzarella, Eloisa Sofia, Pintaudi, Gabriele, Di Muro, Mariangela, Grieco, Domenico Luca, Antonelli, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049343/
https://www.ncbi.nlm.nih.gov/pubmed/35482703
http://dx.doi.org/10.1371/journal.pone.0267038
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author De Pascale, Gennaro
Cutuli, Salvatore Lucio
Carelli, Simone
Xhemalaj, Rikardo
Rosà, Tommaso
Bello, Giuseppe
Vargas, Joel
Cesarano, Melania
Montini, Luca
Tanzarella, Eloisa Sofia
Pintaudi, Gabriele
Di Muro, Mariangela
Grieco, Domenico Luca
Antonelli, Massimo
author_facet De Pascale, Gennaro
Cutuli, Salvatore Lucio
Carelli, Simone
Xhemalaj, Rikardo
Rosà, Tommaso
Bello, Giuseppe
Vargas, Joel
Cesarano, Melania
Montini, Luca
Tanzarella, Eloisa Sofia
Pintaudi, Gabriele
Di Muro, Mariangela
Grieco, Domenico Luca
Antonelli, Massimo
author_sort De Pascale, Gennaro
collection PubMed
description INTRODUCTION: Remdesivir and Dexamethasone represent the cornerstone of therapy for critically ill patients with acute hypoxemic respiratory failure caused by Coronavirus Disease 2019 (COVID-19). However, clinical efficacy and safety of concomitant administration of Remdesivir and Dexamethasone (Rem-Dexa) in severe COVID-19 patients on high flow oxygen therapy (HFOT) or non-invasive ventilation (NIV) remains unknown. MATERIALS AND METHODS: Prospective cohort study that was performed in two medical Intensive Care Units (ICUs) of a tertiary university hospital. The clinical impact of Rem-Dexa administration in hypoxemic patients with COVID-19, who required NIV or HFOT and selected on the simplified acute physiology score II, the sequential organ failure assessment score and the Charlson Comorbidity Index score, was investigated. The primary outcome was 28-day intubation rate; secondary outcomes were end-of-treatment clinical improvement and PaO2/FiO2 ratio, laboratory abnormalities and clinical complications, ICU and hospital length of stay, 28-day and 90-day mortality. RESULTS: We included 132 patients and found that 28-day intubation rate was significantly lower among Rem-Dexa group (19.7% vs 48.5%, p<0.01). Although the end-of-treatment clinical improvement was larger among Rem-Dexa group (69.7% vs 51.5%, p = 0.05), the 28-day and 90-day mortalities were similar (4.5% and 10.6% vs. 15.2% and 16.7%; p = 0.08 and p = 0.45, respectively). The logistic regression and Cox-regression models showed that concomitant Rem-Dexa therapy was associated with a reduction of 28-day intubation rate (OR 0.22, CI95% 0.05–0.94, p = 0.04), in absence of laboratory abnormalities and clinical complications (p = ns). CONCLUSIONS: In COVID-19 critically ill patients receiving HFO or NIV, 28-day intubation rate was lower in patients who received Rem-Dexa and this finding corresponded to lower end-of-treatment clinical improvement. The individual contribution of either Remdesevir or Dexamethasone to the observed clinical effect should be further investigated.
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spelling pubmed-90493432022-04-29 Remdesivir plus Dexamethasone in COVID-19: A cohort study of severe patients requiring high flow oxygen therapy or non-invasive ventilation De Pascale, Gennaro Cutuli, Salvatore Lucio Carelli, Simone Xhemalaj, Rikardo Rosà, Tommaso Bello, Giuseppe Vargas, Joel Cesarano, Melania Montini, Luca Tanzarella, Eloisa Sofia Pintaudi, Gabriele Di Muro, Mariangela Grieco, Domenico Luca Antonelli, Massimo PLoS One Research Article INTRODUCTION: Remdesivir and Dexamethasone represent the cornerstone of therapy for critically ill patients with acute hypoxemic respiratory failure caused by Coronavirus Disease 2019 (COVID-19). However, clinical efficacy and safety of concomitant administration of Remdesivir and Dexamethasone (Rem-Dexa) in severe COVID-19 patients on high flow oxygen therapy (HFOT) or non-invasive ventilation (NIV) remains unknown. MATERIALS AND METHODS: Prospective cohort study that was performed in two medical Intensive Care Units (ICUs) of a tertiary university hospital. The clinical impact of Rem-Dexa administration in hypoxemic patients with COVID-19, who required NIV or HFOT and selected on the simplified acute physiology score II, the sequential organ failure assessment score and the Charlson Comorbidity Index score, was investigated. The primary outcome was 28-day intubation rate; secondary outcomes were end-of-treatment clinical improvement and PaO2/FiO2 ratio, laboratory abnormalities and clinical complications, ICU and hospital length of stay, 28-day and 90-day mortality. RESULTS: We included 132 patients and found that 28-day intubation rate was significantly lower among Rem-Dexa group (19.7% vs 48.5%, p<0.01). Although the end-of-treatment clinical improvement was larger among Rem-Dexa group (69.7% vs 51.5%, p = 0.05), the 28-day and 90-day mortalities were similar (4.5% and 10.6% vs. 15.2% and 16.7%; p = 0.08 and p = 0.45, respectively). The logistic regression and Cox-regression models showed that concomitant Rem-Dexa therapy was associated with a reduction of 28-day intubation rate (OR 0.22, CI95% 0.05–0.94, p = 0.04), in absence of laboratory abnormalities and clinical complications (p = ns). CONCLUSIONS: In COVID-19 critically ill patients receiving HFO or NIV, 28-day intubation rate was lower in patients who received Rem-Dexa and this finding corresponded to lower end-of-treatment clinical improvement. The individual contribution of either Remdesevir or Dexamethasone to the observed clinical effect should be further investigated. Public Library of Science 2022-04-28 /pmc/articles/PMC9049343/ /pubmed/35482703 http://dx.doi.org/10.1371/journal.pone.0267038 Text en © 2022 De Pascale et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
De Pascale, Gennaro
Cutuli, Salvatore Lucio
Carelli, Simone
Xhemalaj, Rikardo
Rosà, Tommaso
Bello, Giuseppe
Vargas, Joel
Cesarano, Melania
Montini, Luca
Tanzarella, Eloisa Sofia
Pintaudi, Gabriele
Di Muro, Mariangela
Grieco, Domenico Luca
Antonelli, Massimo
Remdesivir plus Dexamethasone in COVID-19: A cohort study of severe patients requiring high flow oxygen therapy or non-invasive ventilation
title Remdesivir plus Dexamethasone in COVID-19: A cohort study of severe patients requiring high flow oxygen therapy or non-invasive ventilation
title_full Remdesivir plus Dexamethasone in COVID-19: A cohort study of severe patients requiring high flow oxygen therapy or non-invasive ventilation
title_fullStr Remdesivir plus Dexamethasone in COVID-19: A cohort study of severe patients requiring high flow oxygen therapy or non-invasive ventilation
title_full_unstemmed Remdesivir plus Dexamethasone in COVID-19: A cohort study of severe patients requiring high flow oxygen therapy or non-invasive ventilation
title_short Remdesivir plus Dexamethasone in COVID-19: A cohort study of severe patients requiring high flow oxygen therapy or non-invasive ventilation
title_sort remdesivir plus dexamethasone in covid-19: a cohort study of severe patients requiring high flow oxygen therapy or non-invasive ventilation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049343/
https://www.ncbi.nlm.nih.gov/pubmed/35482703
http://dx.doi.org/10.1371/journal.pone.0267038
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