Evidence map›Paper›PMID 28828366›Full record

ReviewAnnals of translational medicine2017

Sedation and neuromuscular blocking agents in acute respiratory distress syndrome.

Jeremy Bourenne, Sami Hraiech, Antoine Roch, Marc Gainnier, Laurent Papazian, Jean-Marie Forel

Open access · hybridAbstract readReview
In one paragraph

Review in Annals of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 4 pooled it
4.5field-weighted citation impact, top 5% 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

31 citing papers in PubMed, 4 syntheses or guidelines pooled it, 73 citations in OpenAlex.

  1. Pooled it
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  3. ICU-acquired weakness.Intensive care medicine · 2020
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  19. Intensive Care Unit-acquired Weakness: A Frequent but Under-recognized Threat.Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine · 2021
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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

6 authors at 2 institutions in 1 country.

Jeremy BourenneAPHM, Hôpital la Timone, Réanimation des urgences et médicale, Marseille, France.
Sami HraiechCentre d'Études et de Recherche sur les Services de Santé et la Qualité de Vie, CEReSS, Aix-Marseille Université, Faculté de Médecine, Marseille, France.
Antoine RochCentre d'Études et de Recherche sur les Services de Santé et la Qualité de Vie, CEReSS, Aix-Marseille Université, Faculté de Médecine, Marseille, France.
Marc GainnierAPHM, Hôpital la Timone, Réanimation des urgences et médicale, Marseille, France.
Laurent PapazianCentre d'Études et de Recherche sur les Services de Santé et la Qualité de Vie, CEReSS, Aix-Marseille Université, Faculté de Médecine, Marseille, France.
Jean-Marie ForelCentre d'Études et de Recherche sur les Services de Santé et la Qualité de Vie, CEReSS, Aix-Marseille Université, Faculté de Médecine, Marseille, France.
Aix-Marseille Université · FRHôpital Nord · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanical ventilation (MV) is the cornerstone of acute respiratory distress syndrome (ARDS) management. The use of protective ventilation is a priority in this acute phase of lung inflammation. Neuromuscular blocking agents (NMBAs) induce reversible muscle paralysis. Their use in patients with ARDS remains controversial but occurs frequently. NMBAs are used in 25-45% of ARDS patients for a mean period of 1±2 days. The main indications of NMBAs are hypoxemia and facilitation of MV. For ethical reasons, NMBA use is inseparable from sedation in the management of early ARDS. During paralysis, sedation monitoring seems to be necessary to avoid awareness with recall. Three randomized controlled trials (RCTs) have demonstrated that the systematic use of NMBAs in the early management of ARDS patients improves oxygenation. Furthermore, the most recent trial reported a reduction of mortality at 90 days when NMBAs were infused over 48 hours. Spontaneous ventilation (SV) during MV at the acute phase of ARDS could improve oxygenation and alveolar recruitment, but it may not allow protective ventilation. The major risk is an increase in ventilator-induced lung injury. However, the adverse effects of NMBAs are widely discussed, particularly the occurrence of intensive care unit (ICU)-acquired weakness. This review analyses the recent findings in the literature concerning sedation and paralysis in managing ARDS.

Indexed as

Acute respiratory distress syndrome (ARDS)muscle paralysisneuromuscular blocking agent (NMBA)protective ventilationsedationspontaneous breathingtranspulmonary pressure

Identifiers

PMID28828366
PMCPMC5537113
OpenAlexW2739048507

What OpenQuestion holds

Textmetadata
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.