Evidence map›Paper›PMID 36308564›Full record

ArticleAnnals of intensive care2022

Association of early dexamethasone therapy with mortality in critically Ill COVID-19 patients: a French multicenter study.

Matthieu Raymond, Aurélie Le Thuaut, Pierre Asfar, Cédric Darreau, Florian Reizine, Gwenhaël Colin, Charly Dano, Julien Lorber, Baptiste Hourmant, Agathe Delbove and 7 more

Open access · goldAbstract read
In one paragraph

Article in Annals of intensive care, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 11 institutions in 1 country.

Matthieu RaymondService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire Hôtel-Dieu, 30 Bd. Jean Monnet, 44093, Nantes Cedex 1, France.
Aurélie Le ThuautDirection de la recherche, Plateforme de Méthodologie et Biostatistique, CHU de Nantes, Nantes, France.
Pierre AsfarService de Médecine Intensive Reanimation, CHU d'Angers, Angers, France.
Cédric DarreauService de Réanimation Polyvalente, CH du Mans, Le Mans, France.
Florian ReizineService de Médecine Intensive Réanimation, CHU de Rennes, Rennes, France.
Gwenhaël ColinService de Médecine Intensive Réanimation, CHD de La Roche Sur Yon, La Roche-Sur-Yon, France.
Charly DanoService de Réanimation Polyvalente, CH de Cholet, Cholet, France.
Julien LorberService de Réanimation Polyvalente, CH de Saint Nazaire, Saint-Nazaire, France.
Baptiste HourmantService de Médecine Intensive Réanimation, CHU de Brest, Brest, France.
Agathe DelboveService de Réanimation Polyvalente, CH de Vannes, Vannes, France.
Aurélien FrérouService de Réanimation Polyvalente, CH de Saint Malo, Saint Malo, France.
Jean MorinUnité de Soins Intensifs de Pneumologie, CHU de Nantes, Nantes, France.
Pierre Yves EgreteauService de Réanimation Polyvalente, CH de Morlaix, Morlaix, France.
Philippe SeguinService de Réanimation Chirurgicale, CHU de Rennes, Rennes, France.
Jean ReignierService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire Hôtel-Dieu, 30 Bd. Jean Monnet, 44093, Nantes Cedex 1, France.
Jean-Baptiste LascarrouService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire Hôtel-Dieu, 30 Bd. Jean Monnet, 44093, Nantes Cedex 1, France.
Emmanuel CanetService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire Hôtel-Dieu, 30 Bd. Jean Monnet, 44093, Nantes Cedex 1, France. emmanuel.canet@chu-nantes.fr.ORCID http://orcid.org/0000-0002-2143-8082
Centre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Rennes · FRCentre hospitalier Bretagne Atlantique · FRCentre Hospitalier de Lens · FRCentre Hospitalier de Saint-Malo · FRCentre Hospitalier des Pays de Morlaix · FRCentre Hospitalier du Mans · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Saint-Nazaire · FRCentre Hospitalier Universitaire d'Angers · FRRoche (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDexamethasone is recommended for COVID-19 patients who require oxygen therapy. However, its effectiveness in reducing mortality and intubation, and its safety, remain debated. We aimed to investigate whether dexamethasone reduces day-28 mortality in unselected patients with critical COVID-19.

methodsWe performed an observational cohort study in consecutive COVID-19 patients admitted to any of 13 French intensive care units (ICUs) in 2020. The primary objective was to determine whether early dexamethasone therapy was associated with day-28 mortality and the secondary objectives were to assess whether early dexamethasone decreased intubation requirements and to collect adverse events.

resultsOf 1058 included patients, 611 (57.75%) received early dexamethasone (early dexamethasone group), 358 (33.83%) did not receive any steroids (no steroids group), and 89 (8.41%) received late dexamethasone or other steroids. Day-28 mortality was similar between the early dexamethasone and the no steroids groups (15.06% and 14.25%, respectively; P = 0.59). Factors associated with day-28 mortality were older age (adjusted hazard ratio [aHR], 1.06; 1.04-1.09; P < 0.001), worse SOFA score (aHR, 1.13; 1.06-1.20; P < 0.001), and immunocompromised status (aHR, 1.59; 1.01-2.50; P = 0.043). Early dexamethasone was associated with fewer intubations (48.55% vs. 61.49%, P < 0.001) and more ventilator-free days by day 28 (22 [2-28] vs. 17 [1-28] days, P = 0.003), compared to no steroids. Ventilator-associated pneumonia (VAP) was more common with early dexamethasone (HR, 1.29 [1.01-1.63], P = 0.04) than with no steroids, whereas no differences were noted for bloodstream infection, fungal infection, or gastrointestinal bleeding.

conclusionsEarly dexamethasone in critically ill COVID-19 patients was not associated with lower day-28 mortality. However, early dexamethasone was associated with lower intubation needs and more ventilator-free days by day 28. In patients treated with invasive mechanical ventilation, early dexamethasone was associated with a higher risk of VAP.

Indexed as

COVID-19DexamethasoneIntubationMortalityVentilator-associated pneumonia

Identifiers

PMID36308564
PMCPMC9617242
OpenAlexW4307810434

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.