Evidence map›Paper›PMID 40768068›Full record

Trial reportIntensive care medicine2025

Heterogenous treatment effect of neuromuscular blocking agents for moderate-to-severe ARDS: a post hoc Markov model re-analysis of the ACURASYS trial.

Michael Brunini, Jean-Marie Forel, Xavier Muracciole, Antoine Roch, Dominique Barbolosi, Laurent Papazian

Erratum issuedAbstract readRandomized Controlled TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Intensive care medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Update on acute respiratory failure.Intensive care medicine · 2026
    Article
  3. Review
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Michael BruniniUniversità di Corsica Pasquale Paoli, Corte, Corsica, France.
Jean-Marie ForelAssistance Publique-Hôpitaux de Marseille, Hôpital Nord, Médecine Intensive Réanimation, Marseille, France.
Xavier MuraccioleAssistance Publique-Hôpitaux de Marseille, Hôpital Nord, Département Oncologie-Radiothérapie, Aix-Marseille Université, Équipe Inria-Inserm COMPO, Pharmacologie Computationnelle et Oncologie Clinique, Centre Inria Sophia Antipolis-Méditerranée, Centre de Recherches en Cancérologie de Marseille, Inserm U1068, CNRS UMR7258, Institut Paoli-Calmettes, Marseille, France.
Antoine RochAssistance Publique-Hôpitaux de Marseille, Hôpital Nord, Médecine Intensive Réanimation, Marseille, France.
Dominique BarbolosiAix-Marseille Université, Faculté de Pharmacie, Équipe Inria-Inserm COMPO, Pharmacologie Computationnelle et Oncologie Clinique, Centre Inria Sophia Antipolis-Méditerranée, Centre de Recherches en Cancérologie de Marseille, Inserm U1068, CNRS UMR7258, Institut Paoli-Calmettes, Marseille, France.
Laurent PapazianCentre Hospitalier de Bastia, Médecine Intensive Réanimation, Chemin de Falconaja, Bastia, Corsica, France. laurent.papazian.pro@gmail.com.ORCID 0000-0002-8125-9406

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe beneficial effects of systematic cisatracurium administration observed in the ACURASYS randomized, multicenter, double-blinded trial may depend on patient-specific factors. This post hoc analysis aimed to explore whether the impact of cisatracurium on mortality varies with baseline characteristics.

methodsA Markov chain analysis was conducted using daily clinical states from inclusion to day 90: death (state 0), under mechanical ventilation (state 1), or weaned and alive at day 90 (state 2). Patient trajectories were modeled accordingly.

resultsAmong the 321 included patients, subgroup analysis following univariate analysis focused on 130 individuals under 60 years with non-fatal McCabe scores. Within this subgroup, cisatracurium administration and absence of vasopressor use significantly reduced the probability of remaining ventilated. Estimated survival increased therefore from 0.63 (placebo group, N = 62) to 0.93 (cisatracurium group, N = 68). In contrast, among patients with a rapidly or ultimately fatal prognosis according to McCabe score, the probability of survival did not differ substantially between the placebo and cisatracurium groups. Among patients with a PaO

conclusionThe systematic and short-term administration of cisatracurium in patients with moderate-to-severe ARDS appears to confer greater survival benefit in those with a higher baseline life expectancy. Further validation through retrospective and prospective studies is warranted.

Indexed as

AtracuriumNeuromuscular Blocking AgentsRespiratory Distress SyndromeAdultAgedDouble-Blind MethodFemaleHumansMaleMarkov ChainsMiddle AgedRespiration, ArtificialTreatment OutcomeAtracuriumcisatracuriumNeuromuscular Blocking AgentsAcute respiratory distress syndrome (ARDS)CisatracuriumMarkov chain analysisMechanical ventilationMortality predictors

Identifiers

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.