Evidence map›Paper›PMID 33134937›Full record

ArticleCritical care explorations2020

Neuron-Specific Enolase Levels in Adults Under Venoarterial Extracorporeal Membrane Oxygenation.

Jean Reuter, Katell Peoc'h, Lila Bouadma, Stéphane Ruckly, Valérie Chicha-Cattoir, Dorothée Faille, Marie-Charlotte Bourrienne, Claire Dupuis, Eric Magalhaes, Sébastien Tanaka and 9 more

Open access · goldAbstract read
In one paragraph

Article in Critical care explorations, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  3. Observational
  4. Review
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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

19 authors at 6 institutions in 1 country.

Jean ReuterUniversité de Paris, INSERM UMR1148, Team 6, Paris, France.
Katell Peoc'hDepartment of Biochemistry, Beaujon University Hospital, AP-HP, Bichat-Claude Bernard Hospital, Clichy, France.
Lila BouadmaDepartment of Intensive Care Medicine, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Stéphane RucklyUniversité de Paris, INSERM UMR1148, Team 6, Paris, France.
Valérie Chicha-CattoirDepartment of Biochemistry, Beaujon University Hospital, AP-HP, Bichat-Claude Bernard Hospital, Clichy, France.
Dorothée FailleUniversité de Paris, INSERM UMR1148, Team 6, Paris, France.
Marie-Charlotte BourrienneUniversité de Paris, INSERM UMR1148, Team 6, Paris, France.
Claire DupuisDepartment of Intensive Care Medicine, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Eric MagalhaesDepartment of Intensive Care Medicine, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Sébastien TanakaDepartment of Anesthesiology and Intensive Care, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Camille VinclairDepartment of Intensive Care Medicine, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Etienne de MontmollinDepartment of Intensive Care Medicine, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Mikael MazighiUniversité de Paris, INSERM UMR1148, Team 6, Paris, France.
Marylou ParaDepartment of Cardiac Surgery, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Wael BrahamDepartment of Cardiac Surgery, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Angelo PisaniDepartment of Cardiac Surgery, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Nadine AjzenbergUniversité de Paris, INSERM UMR1148, Team 6, Paris, France.
Jean-François TimsitDepartment of Intensive Care Medicine, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
Romain SonnevilleUniversité de Paris, INSERM UMR1148, Team 6, Paris, France.
Inserm · FRUniversité Paris Cité · FRHôpital Bichat-Claude-Bernard · FRAssistance Publique – Hôpitaux de Paris · FRHôpital Lariboisière · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe aimed to determine if elevations in serum neuron-specific enolase are associated with brain injury and outcomes in adults who require venoarterial extracorporeal membrane oxygenation.

designProspective observational study.

settingTwo ICUs of a university hospital, Paris, France. PATIENTS: Consecutive adult patients treated with venoarterial extracorporeal membrane oxygenation for refractory cardiogenic shock or in-hospital refractory cardiac arrest.

interventionsNone. MEASUREMENTS AND MAIN

resultsSerum sampled 1, 3, and 7 days after venoarterial extracorporeal membrane oxygenation cannulation was stored at -80°C and neuron-specific enolase concentrations were measured in batches at the end of the study. The association between neuron-specific enolase concentrations and outcomes (28-d mortality and poor outcome, defined by a score of 4-6 on the modified Rankin scale at 90 d) were explored by multivariable logistic regression, with neuron-specific enolase concentrations dichotomized according to median values. One-hundred three patients were included, of whom 26 (25%) received preextracorporeal membrane oxygenation cardiopulmonary resuscitation. Median (interquartile range) day-1, day-3, and day-7 neuron-specific enolase serum concentrations were 37 μg/L (26-51 μg/L), 25 μg/L (19-37) μg/L, and 22 μg/L (17-31 μg/L). After adjustment for Simplified Acute Physiology Score II, preextracorporeal membrane oxygenation cardiopulmonary resuscitation, and Sepsis Organ Failure Assessment score at time of cannulation, a day-3 neuron-specific enolase greater than 25 μg/L remained independently associated with 28-day mortality (adjusted odds ratio, 4.98; 95% CI, 1.86-13.32) and poor outcome at 90 days (adjusted odds ratio, 4.63; 95% CI, 1.81-11.84). A day-3 neuron-specific enolase threshold greater than 80 μg/L had a 100% specificity for prediction of both mortality (95% CI, 92-100%) and poor functional outcome (95% CI, 89-100%). In a subset of patients who underwent brain CT, neuron-specific enolase concentrations were significantly higher in patients diagnosed with stroke, as compared with those without stroke.

conclusionsIn adult patients under venoarterial extracorporeal membrane oxygenation, day-3 serum neuron-specific enolase concentrations are independently associated with short-term mortality and poor functional outcomes. These findings deserve validation in a multicenter setting.

Indexed as

extracorporeal membrane oxygenationneuron-specific enolaseoutcomestroke

Identifiers

PMID33134937
PMCPMC7566864
OpenAlexW3095273747

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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.