Dexamethasone use and mortality in hospitalized patients with coronavirus disease 2019: A multicentre retrospective observational study.


Journal

British journal of clinical pharmacology
ISSN: 1365-2125
Titre abrégé: Br J Clin Pharmacol
Pays: England
ID NLM: 7503323

Informations de publication

Date de publication:
10 2021
Historique:
revised: 30 01 2021
received: 19 11 2020
accepted: 10 02 2021
pubmed: 21 2 2021
medline: 2 10 2021
entrez: 20 2 2021
Statut: ppublish

Résumé

To examine the association between dexamethasone use and mortality among patients hospitalized for COVID-19. We examined the association between dexamethasone use and mortality at AP-HP Greater Paris University hospitals. Study baseline was defined as the date of hospital admission. The primary endpoint was time to death. We compared this endpoint between patients who received dexamethasone and those who did not in time-to-event analyses adjusted for patient characteristics (such as age, sex and comorbidity) and clinical and biological markers of clinical severity of COVID-19, and stratified by the need for respiratory support, i.e. mechanical ventilation or oxygen. The primary analysis was a multivariable Cox regression model. Of 12 217 adult patients hospitalized with a positive COVID-19 reverse transcriptase-polymerase chain reaction test, 171 (1.4%) received dexamethasone orally or by intravenous perfusion during the visit. Among patients who required respiratory support, the end-point occurred in 10/63 (15.9%) patients who received dexamethasone and 298/1129 (26.4%) patients who did not. In this group, there was a significant association between dexamethasone use and reduced mortality in the primary analysis (hazard ratio, 0.46; 95% confidence interval 0.22-0.96, P = .039). Among patients who did not require respiratory support, there was no significant association between dexamethasone use and the endpoint. In this multicentre observational study, dexamethasone use administered either orally or by intravenous injection at a cumulative dose between 60 mg and 150 mg was associated with reduced mortality among patients with COVID-19 requiring respiratory support.

Identifiants

pubmed: 33608891
doi: 10.1111/bcp.14784
pmc: PMC8013383
doi:

Substances chimiques

Dexamethasone 7S5I7G3JQL

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

3766-3775

Informations de copyright

© 2021 British Pharmacological Society.

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Auteurs

Nicolas Hoertel (N)

Département de Psychiatrie, AP-HP.Centre, Hôpital Corentin-Celton, Issy-les-Moulineaux, France.
Institut de Psychiatrie et Neurosciences de Paris, Université de Paris, INSERM, Paris, France.
Faculté de Santé, UFR de Médecine, Université de Paris, Paris, France.

Marina Sánchez-Rico (M)

Département de Psychiatrie, AP-HP.Centre, Hôpital Corentin-Celton, Issy-les-Moulineaux, France.
Department of Psychobiology & Behavioural Sciences Methods, Faculty of Psychology, Universidad Complutense de Madrid, Campus de Somosaguas, Pozuelo de Alarcon, Spain.

Raphaël Vernet (R)

Hôpital Européen Georges Pompidou, Medical Informatics, Biostatistics and Public Health Department, AP-HP.Centre-Université de Paris, Paris, France.

Nathanaël Beeker (N)

Unité de Recherche clinique, Hopital Cochin, Assistance Publique-Hopitaux de Paris, Paris, France.

Antoine Neuraz (A)

INSERM, UMR_S 1138, Cordeliers Research Center, Université de Paris, France.
Department of Medical Informatics, Necker-Enfants Malades Hospital, AP-HP. Centre-Université de Paris, Paris, France.

Jesús M Alvarado (JM)

Department of Psychobiology & Behavioural Sciences Methods, Faculty of Psychology, Universidad Complutense de Madrid, Campus de Somosaguas, Pozuelo de Alarcon, Spain.

Christel Daniel (C)

AP-HP, DSI-WIND (Web Innovation Données), Paris, France.
Sorbonne University, University Paris 13, Sorbonne Paris Cité, INSERM UMR_S 1142, Paris, France.

Nicolas Paris (N)

AP-HP, DSI-WIND (Web Innovation Données), Paris, France.
LIMSI, CNRS, Université Paris-Sud, Université Paris-Saclay, Orsay, France.

Alexandre Gramfort (A)

Université Paris-Saclay, INRIA, CEA, Palaiseau, France.

Guillaume Lemaitre (G)

Université Paris-Saclay, INRIA, CEA, Palaiseau, France.

Elisa Salamanca (E)

Banque Nationale de Données Maladies Rares (BNDMR), Campus Picpus, Département WIND (Web Innovation Données), Paris, France.

Mélodie Bernaux (M)

Direction de la stratégie et de la transformation, AP-HP, Paris, France.

Ali Bellamine (A)

Unité de Recherche clinique, Hôpital Cochin, AP-HP.Centre-Université de Paris, Paris, France.

Anita Burgun (A)

INSERM, UMR_S 1138, Cordeliers Research Center, Université de Paris, France.

Frédéric Limosin (F)

Département de Psychiatrie, AP-HP.Centre, Hôpital Corentin-Celton, Issy-les-Moulineaux, France.
Institut de Psychiatrie et Neurosciences de Paris, Université de Paris, INSERM, Paris, France.
Faculté de Santé, UFR de Médecine, Université de Paris, Paris, France.

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