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

COVID-19 dexamethasone methylprednisolone mortality pulse therapy

Journal

Critical care explorations
ISSN: 2639-8028
Titre abrégé: Crit Care Explor
Pays: United States
ID NLM: 101746347

Informations de publication

Date de publication:
Apr 2023
Historique:
medline: 1 4 2023
entrez: 31 3 2023
pubmed: 1 4 2023
Statut: epublish

Résumé

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. To compare pulse methylprednisolone to dexamethasone as a COVID-19 treatment. 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. 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. 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. 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.

Identifiants

pubmed: 36998527
doi: 10.1097/CCE.0000000000000886
pmc: PMC10047604
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e0886

Informations de copyright

Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine.

Déclaration de conflit d'intérêts

The authors have disclosed that they do not have any potential conflicts of interest.

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Auteurs

Atsuyuki Watanabe (A)

Division of Hospital Medicine, University of Tsukuba Hospital, Tsukuba, Japan.

Ryota Inokuchi (R)

Department of Health Services Research, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.

Toshiki Kuno (T)

Division of Cardiology, Montefiore Medical Center, Albert Einstein College of Medicine, New York, NY.

Kazuaki Uda (K)

Department of Health Services Research, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.

Jun Komiyama (J)

Department of Health Services Research, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.

Motohiko Adomi (M)

Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA.

Yoshiko Ishisaka (Y)

Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, New York, NY.

Toshikazu Abe (T)

Department of Health Services Research, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.
Department of Emergency and Critical Care Medicine, Tsukuba Memorial Hospital, Tsukuba, Japan.

Nanako Tamiya (N)

Department of Health Services Research, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.

Masao Iwagami (M)

Department of Health Services Research, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.
Department of Non-Communicable Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Classifications MeSH