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Pulse Methylprednisolone Versus Dexamethasone in COVID-19: A Multicenter Cohort Study

Although pulse (high-dose) methylprednisolone therapy can hypothetically control immune system flare-ups effectively, the clinical benefit of pulse methylprednisolone compared with dexamethasone in COVID-19 remains inconclusive. OBJECTIVES: To compare pulse methylprednisolone to dexamethasone as a C...

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Autores principales: Watanabe, Atsuyuki, Inokuchi, Ryota, Kuno, Toshiki, Uda, Kazuaki, Komiyama, Jun, Adomi, Motohiko, Ishisaka, Yoshiko, Abe, Toshikazu, Tamiya, Nanako, Iwagami, Masao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047604/
https://www.ncbi.nlm.nih.gov/pubmed/36998527
http://dx.doi.org/10.1097/CCE.0000000000000886
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author Watanabe, Atsuyuki
Inokuchi, Ryota
Kuno, Toshiki
Uda, Kazuaki
Komiyama, Jun
Adomi, Motohiko
Ishisaka, Yoshiko
Abe, Toshikazu
Tamiya, Nanako
Iwagami, Masao
author_facet Watanabe, Atsuyuki
Inokuchi, Ryota
Kuno, Toshiki
Uda, Kazuaki
Komiyama, Jun
Adomi, Motohiko
Ishisaka, Yoshiko
Abe, Toshikazu
Tamiya, Nanako
Iwagami, Masao
author_sort Watanabe, Atsuyuki
collection PubMed
description Although pulse (high-dose) methylprednisolone therapy can hypothetically control immune system flare-ups effectively, the clinical benefit of pulse methylprednisolone compared with dexamethasone in COVID-19 remains inconclusive. OBJECTIVES: To compare pulse methylprednisolone to dexamethasone as a COVID-19 treatment. DESIGN, SETTING, AND PARTICIPANTS: Using a Japanese multicenter database, we identified adult patients admitted for COVID-19 and discharged between January 2020 and December 2021 treated with pulse methylprednisolone (250, 500, or 1,000 mg/d) or IV dexamethasone (≥ 6 mg/d) at admission day 0 or 1. MAIN OUTCOMES AND MEASURES: The primary outcome was in-hospital mortality. Secondary outcomes were 30-day mortality, new ICU admission, insulin initiation, fungal infection, and readmission. Multivariable logistic regression was conducted to differentiate the dose of pulse methylprednisolone (250, 500, or 1,000 mg/d). Additionally, subgroup analyses by characteristics such as the need for invasive mechanical ventilation (IMV) were also conducted. RESULTS: A total of 7,519, 197, 399, and 1,046 patients received dexamethasone, 250, 500, and 1,000 mg/d of methylprednisolone, respectively. The crude in-hospital mortality was 9.3% (702/7,519), 8.6% (17/197), 17.0% (68/399), and 16.2% (169/1,046) for the different doses, respectively. The adjusted odds ratio (95% CI) was 1.26 (0.69–2.29), 1.48 (1.07–2.04), and 1.75 (1.40–2.19) in patients starting 250, 500, and 1,000 mg/d of methylprednisolone, respectively, compared with those starting dexamethasone. In subgroup analyses, the adjusted odds ratio of in-hospital mortality was 0.78 (0.25–2.47), 1.12 (0.55–2.27), and 1.04 (0.68–1.57) in 250, 500, and 1,000 mg/d of methylprednisolone, respectively, among patients with IMV, whereas the adjusted odds ratio was 1.54 (0.77–3.08), 1.62 (1.13–2.34), and 2.14 (1.64–2.80) among patients without IMV. CONCLUSIONS AND RELEVANCE: Higher doses of pulse methylprednisolone (500 or 1,000 mg/d) may be associated with worse COVID-19 outcomes when compared with dexamethasone, especially in patients not on IMV.
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spelling pubmed-100476042023-03-29 Pulse Methylprednisolone Versus Dexamethasone in COVID-19: A Multicenter Cohort Study Watanabe, Atsuyuki Inokuchi, Ryota Kuno, Toshiki Uda, Kazuaki Komiyama, Jun Adomi, Motohiko Ishisaka, Yoshiko Abe, Toshikazu Tamiya, Nanako Iwagami, Masao Crit Care Explor Observational Study Although pulse (high-dose) methylprednisolone therapy can hypothetically control immune system flare-ups effectively, the clinical benefit of pulse methylprednisolone compared with dexamethasone in COVID-19 remains inconclusive. OBJECTIVES: To compare pulse methylprednisolone to dexamethasone as a COVID-19 treatment. DESIGN, SETTING, AND PARTICIPANTS: Using a Japanese multicenter database, we identified adult patients admitted for COVID-19 and discharged between January 2020 and December 2021 treated with pulse methylprednisolone (250, 500, or 1,000 mg/d) or IV dexamethasone (≥ 6 mg/d) at admission day 0 or 1. MAIN OUTCOMES AND MEASURES: The primary outcome was in-hospital mortality. Secondary outcomes were 30-day mortality, new ICU admission, insulin initiation, fungal infection, and readmission. Multivariable logistic regression was conducted to differentiate the dose of pulse methylprednisolone (250, 500, or 1,000 mg/d). Additionally, subgroup analyses by characteristics such as the need for invasive mechanical ventilation (IMV) were also conducted. RESULTS: A total of 7,519, 197, 399, and 1,046 patients received dexamethasone, 250, 500, and 1,000 mg/d of methylprednisolone, respectively. The crude in-hospital mortality was 9.3% (702/7,519), 8.6% (17/197), 17.0% (68/399), and 16.2% (169/1,046) for the different doses, respectively. The adjusted odds ratio (95% CI) was 1.26 (0.69–2.29), 1.48 (1.07–2.04), and 1.75 (1.40–2.19) in patients starting 250, 500, and 1,000 mg/d of methylprednisolone, respectively, compared with those starting dexamethasone. In subgroup analyses, the adjusted odds ratio of in-hospital mortality was 0.78 (0.25–2.47), 1.12 (0.55–2.27), and 1.04 (0.68–1.57) in 250, 500, and 1,000 mg/d of methylprednisolone, respectively, among patients with IMV, whereas the adjusted odds ratio was 1.54 (0.77–3.08), 1.62 (1.13–2.34), and 2.14 (1.64–2.80) among patients without IMV. CONCLUSIONS AND RELEVANCE: Higher doses of pulse methylprednisolone (500 or 1,000 mg/d) may be associated with worse COVID-19 outcomes when compared with dexamethasone, especially in patients not on IMV. Lippincott Williams & Wilkins 2023-03-27 /pmc/articles/PMC10047604/ /pubmed/36998527 http://dx.doi.org/10.1097/CCE.0000000000000886 Text en Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Observational Study
Watanabe, Atsuyuki
Inokuchi, Ryota
Kuno, Toshiki
Uda, Kazuaki
Komiyama, Jun
Adomi, Motohiko
Ishisaka, Yoshiko
Abe, Toshikazu
Tamiya, Nanako
Iwagami, Masao
Pulse Methylprednisolone Versus Dexamethasone in COVID-19: A Multicenter Cohort Study
title Pulse Methylprednisolone Versus Dexamethasone in COVID-19: A Multicenter Cohort Study
title_full Pulse Methylprednisolone Versus Dexamethasone in COVID-19: A Multicenter Cohort Study
title_fullStr Pulse Methylprednisolone Versus Dexamethasone in COVID-19: A Multicenter Cohort Study
title_full_unstemmed Pulse Methylprednisolone Versus Dexamethasone in COVID-19: A Multicenter Cohort Study
title_short Pulse Methylprednisolone Versus Dexamethasone in COVID-19: A Multicenter Cohort Study
title_sort pulse methylprednisolone versus dexamethasone in covid-19: a multicenter cohort study
topic Observational Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047604/
https://www.ncbi.nlm.nih.gov/pubmed/36998527
http://dx.doi.org/10.1097/CCE.0000000000000886
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