Evidence map›Paper›PMID 35918776›Full record

ArticleCritical care (London, England)2022

Early steroids and ventilator-associated pneumonia in COVID-19-related ARDS.

Pauline Lamouche-Wilquin, Jérôme Souchard, Morgane Pere, Matthieu Raymond, Pierre Asfar, Cédric Darreau, Florian Reizine, Baptiste Hourmant, Gwenhaël Colin, Guillaume Rieul and 12 more

Open access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 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

22 authors at 13 institutions in 1 country.

Pauline Lamouche-WilquinService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Nantes, 1 Place Alexis Ricordeau, 44093, Nantes Cedex 01, France.
Jérôme SouchardService de Réanimation Polyvalente, Centre Hospitalier Bretagne Atlantique, Vannes, France.
Morgane PerePlateforme de Méthodologie et Biostatistique, Centre Hospitalier Universitaire de Nantes, Nantes, France.
Matthieu RaymondService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Nantes, 1 Place Alexis Ricordeau, 44093, Nantes Cedex 01, France.
Pierre AsfarService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire d'Angers, Angers, France.
Cédric DarreauService de Réanimation Polyvalente, Centre Hospitalier du Mans, Le Mans, France.
Florian ReizineService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Rennes, Rennes, France.
Baptiste HourmantService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Brest, Brest, France.
Gwenhaël ColinService de Médecine Intensive Réanimation, Centre Hospitalier Départemental de Vendée, La Roche-sur-Yon, France.
Guillaume RieulService de Réanimation Polyvalente, Centre Hospitalier Bretagne Atlantique, Vannes, France.
Pierre KergoatService de Réanimation Polyvalente, Centre Hospitalier de Cornouaille, Quimper, France.
Aurélien FrérouService de Réanimation Polyvalente, Centre Hospitalier de Saint-Malo, Saint-Malo, France.
Julien LorberService de Médecine Intensive Réanimation, Centre Hospitalier de Saint-Nazaire, Saint-Nazaire, France.
Johann AuchabieService de Réanimation Polyvalente, Centre Hospitalier de Cholet, Cholet, France.
Béatrice La CombeService de Réanimation Polyvalente, Centre Hospitalier Bretagne Sud, Lorient, France.
Philippe SeguinService de Réanimation Chirurgicale, Centre Hospitalier Universitaire de Rennes, Rennes, France.
Pierre-Yves EgreteauService de Réanimation Polyvalente, Centre Hospitalier de Morlaix, Morlaix, France.
Jean MorinService de Soins Intensifs de Pneumologie, Centre Hospitalier Universitaire de Nantes, Nantes, France.
Yannick FedunService de Réanimation Polyvalente, Centre Hospitalier Bretagne Atlantique, Vannes, France.
Emmanuel CanetService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Nantes, 1 Place Alexis Ricordeau, 44093, Nantes Cedex 01, France.
Jean-Baptiste LascarrouService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Nantes, 1 Place Alexis Ricordeau, 44093, Nantes Cedex 01, France. jeanbaptiste.lascarrou@chu-nantes.fr.
Agathe DelboveService de Réanimation Polyvalente, Centre Hospitalier Bretagne Atlantique, Vannes, France.
Centre Hospitalier Universitaire de Nantes · FRCentre hospitalier Bretagne Atlantique · FRCentre Hospitalier Universitaire de Rennes · FRCentre Hospitalier de Bretagne Sud · FRCentre Hospitalier de Cornouaille · FRCentre Hospitalier de Lens · FRCentre Hospitalier Départemental Vendée · 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 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleEarly corticosteroid treatment is used to treat COVID-19-related acute respiratory distress syndrome (ARDS). Infection is a well-documented adverse effect of corticosteroid therapy.

objectivesTo determine whether early corticosteroid therapy to treat COVID-19 ARDS was associated with ventilator-associated pneumonia (VAP).

methodsWe retrospectively included adults with COVID-19-ARDS requiring invasive mechanical ventilation (MV) for ≥ 48 h at any of 15 intensive care units in 2020. We divided the patients into two groups based on whether they did or did not receive corticosteroids within 24 h. The primary outcome was VAP incidence, with death and extubation as competing events. Secondary outcomes were day 90-mortality, MV duration, other organ dysfunctions, and VAP characteristics. MEASUREMENTS AND MAIN

resultsOf 670 patients (mean age, 65 years), 369 did and 301 did not receive early corticosteroids. The cumulative VAP incidence was higher with early corticosteroids (adjusted hazard ratio [aHR] 1.29; 95% confidence interval [95% CI] 1.05-1.58; P = 0.016). Antibiotic resistance of VAP bacteria was not different between the two groups (odds ratio 0.94, 95% CI 0.58-1.53; P = 0.81). 90-day mortality was 30.9% with and 24.3% without early corticosteroids, a nonsignificant difference after adjustment on age, SOFA score, and VAP occurrence (aHR 1.15; 95% CI 0.83-1.60; P = 0.411). VAP was associated with higher 90-day mortality (aHR 1.86; 95% CI 1.33-2.61; P = 0.0003).

conclusionsEarly corticosteroid treatment was associated with VAP in patients with COVID-19-ARDS. Although VAP was associated with higher 90-day mortality, early corticosteroid treatment was not. Longitudinal randomized controlled trials of early corticosteroids in COVID-19-ARDS requiring MV are warranted.

Indexed as

COVID-19Pneumonia, Ventilator-AssociatedRespiratory Distress SyndromeAdrenal Cortex HormonesAdultAgedHumansIntensive Care UnitsRespiration, ArtificialRetrospective StudiesSteroidsAdrenal Cortex HormonesSteroidsDexamethasoneMechanical ventilationMethylprednisoloneNosocomial pneumoniaSARS-CoV-19

Identifiers

PMID35918776
PMCPMC9344449
OpenAlexW4289522791

What OpenQuestion holds

Textmetadata
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.