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Safety and efficacy of methylprednisolone versus dexamethasone in critically ill patients with COVID-19 acute respiratory distress syndrome: a retrospective study

BACKGROUND: Corticosteroids (CSs), specifically dexamethasone (DEX), are the treatment of choice for severe acute respiratory distress syndrome (ARDS) due to COVID-19 pneumonia (CARDS). However, data from both ARDS and relatively small CARDS clinical trials have suggested improved outcomes with meth...

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Autores principales: Kellogg, Dean, Gutierrez, G. Christina, Small, Clay E., Stephens, Benjamin, Sanchez, Paloma, Beg, Moezzullah, Keyt, Holly L., Restrepo, Marcos I., Attridge, Rebecca L., Maselli, Diego J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936170/
https://www.ncbi.nlm.nih.gov/pubmed/36818803
http://dx.doi.org/10.1177/20499361231153546
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author Kellogg, Dean
Gutierrez, G. Christina
Small, Clay E.
Stephens, Benjamin
Sanchez, Paloma
Beg, Moezzullah
Keyt, Holly L.
Restrepo, Marcos I.
Attridge, Rebecca L.
Maselli, Diego J.
author_facet Kellogg, Dean
Gutierrez, G. Christina
Small, Clay E.
Stephens, Benjamin
Sanchez, Paloma
Beg, Moezzullah
Keyt, Holly L.
Restrepo, Marcos I.
Attridge, Rebecca L.
Maselli, Diego J.
author_sort Kellogg, Dean
collection PubMed
description BACKGROUND: Corticosteroids (CSs), specifically dexamethasone (DEX), are the treatment of choice for severe acute respiratory distress syndrome (ARDS) due to COVID-19 pneumonia (CARDS). However, data from both ARDS and relatively small CARDS clinical trials have suggested improved outcomes with methylprednisolone (MP) versus DEX. The objective of this retrospective cohort study was to compare the safety and effectiveness of MP and DEX in critically ill CARDS patients. METHODS: The study cohort included CARDS patients admitted to a tertiary referral intensive care unit (ICU) between April and September 2020 who received at least 5 days of CSs for CARDS. RESULTS: The cohort was notable for a high severity of illness (overall, 88.5% of patients required mechanical ventilation and 16% required vasopressors on admission). The DEX group (n = 62) was significantly older with a higher illness severity [Sequential Organ Failure Assessment (SOFA) 6 (4.75–8) versus 4.5 (3–7), p = 0.008], while the MP group (n = 51) received significantly more loading doses [19 (37.3%) versus 4 (6.5%), p < 0.0001]. MP was associated with a shorter time to intubation and more rapid progression to mortality [days to death: 18 (15–23) versus 27 (15–34), p = 0.026]. After correction for baseline imbalances in age and SOFA score, DEX was associated with improved mortality at 90 days compared with MP [hazard ratio (HR) = 0.43, 95% confidence interval (CI) = 0.23–0.80, p = 0.008]. However, there were no differences between rates of secondary infections during hospitalization or insulin requirements at 7 and 14 days. CONCLUSION: In this cohort of critically ill CARDS, choice of CS was associated with mortality but not adverse event profile, and thus warrants further investigation.
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spelling pubmed-99361702023-02-18 Safety and efficacy of methylprednisolone versus dexamethasone in critically ill patients with COVID-19 acute respiratory distress syndrome: a retrospective study Kellogg, Dean Gutierrez, G. Christina Small, Clay E. Stephens, Benjamin Sanchez, Paloma Beg, Moezzullah Keyt, Holly L. Restrepo, Marcos I. Attridge, Rebecca L. Maselli, Diego J. Ther Adv Infect Dis Original Research BACKGROUND: Corticosteroids (CSs), specifically dexamethasone (DEX), are the treatment of choice for severe acute respiratory distress syndrome (ARDS) due to COVID-19 pneumonia (CARDS). However, data from both ARDS and relatively small CARDS clinical trials have suggested improved outcomes with methylprednisolone (MP) versus DEX. The objective of this retrospective cohort study was to compare the safety and effectiveness of MP and DEX in critically ill CARDS patients. METHODS: The study cohort included CARDS patients admitted to a tertiary referral intensive care unit (ICU) between April and September 2020 who received at least 5 days of CSs for CARDS. RESULTS: The cohort was notable for a high severity of illness (overall, 88.5% of patients required mechanical ventilation and 16% required vasopressors on admission). The DEX group (n = 62) was significantly older with a higher illness severity [Sequential Organ Failure Assessment (SOFA) 6 (4.75–8) versus 4.5 (3–7), p = 0.008], while the MP group (n = 51) received significantly more loading doses [19 (37.3%) versus 4 (6.5%), p < 0.0001]. MP was associated with a shorter time to intubation and more rapid progression to mortality [days to death: 18 (15–23) versus 27 (15–34), p = 0.026]. After correction for baseline imbalances in age and SOFA score, DEX was associated with improved mortality at 90 days compared with MP [hazard ratio (HR) = 0.43, 95% confidence interval (CI) = 0.23–0.80, p = 0.008]. However, there were no differences between rates of secondary infections during hospitalization or insulin requirements at 7 and 14 days. CONCLUSION: In this cohort of critically ill CARDS, choice of CS was associated with mortality but not adverse event profile, and thus warrants further investigation. SAGE Publications 2023-02-15 /pmc/articles/PMC9936170/ /pubmed/36818803 http://dx.doi.org/10.1177/20499361231153546 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Kellogg, Dean
Gutierrez, G. Christina
Small, Clay E.
Stephens, Benjamin
Sanchez, Paloma
Beg, Moezzullah
Keyt, Holly L.
Restrepo, Marcos I.
Attridge, Rebecca L.
Maselli, Diego J.
Safety and efficacy of methylprednisolone versus dexamethasone in critically ill patients with COVID-19 acute respiratory distress syndrome: a retrospective study
title Safety and efficacy of methylprednisolone versus dexamethasone in critically ill patients with COVID-19 acute respiratory distress syndrome: a retrospective study
title_full Safety and efficacy of methylprednisolone versus dexamethasone in critically ill patients with COVID-19 acute respiratory distress syndrome: a retrospective study
title_fullStr Safety and efficacy of methylprednisolone versus dexamethasone in critically ill patients with COVID-19 acute respiratory distress syndrome: a retrospective study
title_full_unstemmed Safety and efficacy of methylprednisolone versus dexamethasone in critically ill patients with COVID-19 acute respiratory distress syndrome: a retrospective study
title_short Safety and efficacy of methylprednisolone versus dexamethasone in critically ill patients with COVID-19 acute respiratory distress syndrome: a retrospective study
title_sort safety and efficacy of methylprednisolone versus dexamethasone in critically ill patients with covid-19 acute respiratory distress syndrome: a retrospective study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936170/
https://www.ncbi.nlm.nih.gov/pubmed/36818803
http://dx.doi.org/10.1177/20499361231153546
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