Evidence map›Paper›PMID 35628922›Full record

ArticleJournal of clinical medicine2022

Design and Rationale of the Sevoflurane for Sedation in Acute Respiratory Distress Syndrome (SESAR) Randomized Controlled Trial.

Raiko Blondonnet, Laure-Anne Simand, Perine Vidal, Lucile Borao, Nathalie Bourguignon, Dominique Morand, Lise Bernard, Laurence Roszyk, Jules Audard, Thomas Godet and 15 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
6.8field-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

8 citing papers in PubMed, 44 citations in OpenAlex.

  1. Volatile anesthetics in the intensive care unit.Anaesthesiology intensive therapy · 2025
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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

25 authors at 6 institutions in 2 countries.

Raiko BlondonnetDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Laure-Anne SimandDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Perine VidalDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.ORCID 0000-0002-2600-1138
Lucile BoraoDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Nathalie BourguignonDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Dominique MorandDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Lise BernardDepartment of Clinical Research and Temporary Authorization, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.ORCID 0000-0002-1159-0048
Laurence RoszykiGReD, Université Clermont Auvergne, CNRS, INSERM, 63000 Clermont-Ferrand, France.
Jules AudardDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Thomas GodetDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Antoine MonselDepartment of Anesthesiology and Critical Care, GRC 29, DMU DREAM, Pitié-Salpêtrière Hospital, Sorbonne University, Assistance Publique-Hôpitaux de Paris, 75013 Paris, France.
Marc GarnierDepartment of Anesthesiology and Critical Care Medicine, DMU DREAM, Saint-Antoine University Hospital, Sorbonne University, Assistance Publique-Hôpitaux de Paris, 75012 Paris, France.
Christophe QuesnelDepartment of Anesthesiology and Critical Care Medicine, DMU DREAM, Tenon University Hospital, Sorbonne University, Assistance Publique-Hôpitaux de Paris, 75020 Paris, France.
Jean-Etienne BazinDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Vincent SapiniGReD, Université Clermont Auvergne, CNRS, INSERM, 63000 Clermont-Ferrand, France.ORCID 0000-0002-7452-315X
Julie A BastaracheDivision of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Lorraine B WareDivision of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0002-9429-4702
Christopher G HughesDivision of Anesthesiology Critical Care Medicine, Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Pratik P PandharipandeDivision of Anesthesiology Critical Care Medicine, Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
E Wesley ElyDivision of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Emmanuel FutierDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Bruno PereiraBiostatistics and Data Management Unit, Department of Clinical Research and Innovation (DRCI), CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.ORCID 0000-0003-3778-7161
Jean-Michel ConstantinDepartment of Anesthesiology and Critical Care, GRC 29, DMU DREAM, Pitié-Salpêtrière Hospital, Sorbonne University, Assistance Publique-Hôpitaux de Paris, 75013 Paris, France.ORCID 0000-0001-7634-5898
Matthieu JabaudonDepartment of Perioperative Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.ORCID 0000-0002-8121-1680
On Behalf Of The Sesar Collaborative Group
Centre Hospitalier Universitaire de Clermont-Ferrand · FRCentre National de la Recherche Scientifique · FRSorbonne Université · FRVA Tennessee Valley Healthcare System · USVanderbilt University · USVanderbilt University Medical Center · US

Funding

European Society of Anaesthesiology and Intensive Care Research Grant 2019French Ministry of Health Programme Hospitalier de Recherche Clinique National 2018Sedana Medical Research Grant 2019
6 · The paper itself

Abstract

Preclinical studies have shown that volatile anesthetics may have beneficial effects on injured lungs, and pilot clinical data support improved arterial oxygenation, attenuated inflammation, and decreased lung epithelial injury in patients with acute respiratory distress syndrome (ARDS) receiving inhaled sevoflurane compared to intravenous midazolam. Whether sevoflurane is effective in improving clinical outcomes among patients with ARDS is unknown, and the benefits and risks of inhaled sedation in ARDS require further evaluation. Here, we describe the SESAR (Sevoflurane for Sedation in ARDS) trial designed to address this question. SESAR is a two-arm, investigator-initiated, multicenter, prospective, randomized, stratified, parallel-group clinical trial with blinded outcome assessment designed to test the efficacy of sedation with sevoflurane compared to intravenous propofol in patients with moderate to severe ARDS. The primary outcome is the number of days alive and off the ventilator at 28 days, considering death as a competing event, and the key secondary outcome is 90 day survival. The planned enrollment is 700 adult participants at 37 French academic and non-academic centers. Safety and long-term outcomes will be evaluated, and biomarker measurements will help better understand mechanisms of action. The trial is funded by the French Ministry of Health, the European Society of Anaesthesiology, and Sedana Medical.

Indexed as

acute respiratory distress syndromeclinical trialinhaled sedationsevoflurane

Identifiers

PMID35628922
PMCPMC9147018
OpenAlexW4280553695

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.