Evidence map›Paper›PMID 28466149›Full record

ArticleIntensive care medicine2017

Potentially modifiable factors contributing to sepsis-associated encephalopathy.

Romain Sonneville, Etienne de Montmollin, Julien Poujade, Maïté Garrouste-Orgeas, Bertrand Souweine, Michael Darmon, Eric Mariotte, Laurent Argaud, François Barbier, Dany Goldgran-Toledano and 7 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Intensive care medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 202 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
202citing papers in PubMed, 6 pooled it
7.0field-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

202 citing papers in PubMed, 6 syntheses or guidelines pooled it, 317 citations in OpenAlex.

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142 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 11 institutions in 1 country.

Romain SonnevilleDepartment of Intensive Care Medicine and Infectious Diseases, Hôpital Bichat-Claude Bernard, 46 rue Henri Huchard, 75877, Paris Cedex, France. romain.sonneville@aphp.fr.
Etienne de MontmollinUMR 1137, IAME Team 5, DeSCID: Decision Sciences in Infectious Diseases, Control and Care, Sorbonne Paris Cité, Inserm/Paris Diderot University, Paris, France.
Julien PoujadeDepartment of Intensive Care Medicine and Infectious Diseases, Hôpital Bichat-Claude Bernard, 46 rue Henri Huchard, 75877, Paris Cedex, France.
Maïté Garrouste-OrgeasUMR 1137, IAME Team 5, DeSCID: Decision Sciences in Infectious Diseases, Control and Care, Sorbonne Paris Cité, Inserm/Paris Diderot University, Paris, France.
Bertrand SouweineMedical Intensive Care Unit, Gabriel Montpied University Hospital, Clermont-Ferrand, France.
Michael DarmonMedical Intensive Care Unit, Saint Etienne University Hospital, Saint-Etienne, France.
Eric MariotteMedical Intensive Care Unit, AP-HP, Saint Louis Hospital, Paris, France.
Laurent ArgaudMedical Intensive Care Unit, Lyon University Hospital, Lyon, France.
François BarbierMedical Intensive Care Unit, La Source Hospital, Orléans, France.
Dany Goldgran-ToledanoMedical-Surgical Intensive Care Unit, Gonesse Hospital, Gonesse, France.
Guillaume MarcotteSurgical ICU, Edouard Herriot University Hospital, Lyon, France.
Anne-Sylvie DumenilMedical-Surgical Intensive Care Unit, AP-HP, Antoine Béclère University Hospital, Clamart, France.
Samir JamaliMedical-Surgical Intensive Care Medicine Unit, Dourdan Hospital, Dourdan, France.
Guillaume LacaveMedical Intensive Care Unit, André Mignot Hospital, Versailles, France.
Stéphane RucklyUMR 1137, IAME Team 5, DeSCID: Decision Sciences in Infectious Diseases, Control and Care, Sorbonne Paris Cité, Inserm/Paris Diderot University, Paris, France.
Bruno MourvillierDepartment of Intensive Care Medicine and Infectious Diseases, Hôpital Bichat-Claude Bernard, 46 rue Henri Huchard, 75877, Paris Cedex, France.
Jean-François TimsitDepartment of Intensive Care Medicine and Infectious Diseases, Hôpital Bichat-Claude Bernard, 46 rue Henri Huchard, 75877, Paris Cedex, France.
Université Paris Cité · FRHôpital Bichat-Claude-Bernard · FRCentre Hospitalier de Gonesse · FRCentre hospitalier régional d'Orléans · FRHôpital André Mignot · FRHôpital Antoine-Béclère · FRHôpital Edouard Herriot · FRHôpital Saint-Louis · FRHospices Civils de Lyon · FRUniversité Claude Bernard Lyon 1 · FRUniversité Jean Monnet · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIdentifying modifiable factors for sepsis-associated encephalopathy may help improve patient care and outcomes.

methodsWe conducted a retrospective analysis of a prospective multicenter database. Sepsis-associated encephalopathy (SAE) was defined by a score on the Glasgow coma scale (GCS) <15 or when features of delirium were noted. Potentially modifiable risk factors for SAE at ICU admission and its impact on mortality were investigated using multivariate logistic regression analysis and Cox proportional hazard modeling, respectively.

resultsWe included 2513 patients with sepsis at ICU admission, of whom 1341 (53%) had sepsis-associated encephalopathy. After adjusting for baseline characteristics, site of infection, and type of admission, the following factors remained independently associated with sepsis-associated encephalopathy: acute renal failure [adjusted odds ratio (aOR) = 1.41, 95% confidence interval (CI) 1.19-1.67], hypoglycemia <3 mmol/l (aOR = 2.66, 95% CI 1.27-5.59), hyperglycemia >10 mmol/l (aOR = 1.37, 95% CI 1.09-1.72), hypercapnia >45 mmHg (aOR = 1.91, 95% CI 1.53-2.38), hypernatremia >145 mmol/l (aOR = 2.30, 95% CI 1.48-3.57), and S. aureus (aOR = 1.54, 95% CI 1.05-2.25). Sepsis-associated encephalopathy was associated with higher mortality, higher use of ICU resources, and longer hospital stay. After adjusting for age, comorbidities, year of admission, and non-neurological SOFA score, even mild alteration of mental status (i.e., a score on the GCS of 13-14) remained independently associated with mortality (adjusted hazard ratio = 1.38, 95% CI 1.09-1.76).

conclusionsAcute renal failure and common metabolic disturbances represent potentially modifiable factors contributing to sepsis-associated encephalopathy. However, a true causal relationship has yet to be demonstrated. Our study confirms the prognostic significance of mild alteration of mental status in patients with sepsis.

Indexed as

Acute Kidney InjuryAgedDeliriumFemaleGlasgow Coma ScaleHumansIntensive Care UnitsLength of StayMaleMetabolic DiseasesMiddle AgedOrgan Dysfunction ScoresProportional Hazards ModelsProspective StudiesRetrospective StudiesRisk FactorsAcute renal failureBrain injuryDeliriumEncephalopathyOutcomeSepsis

Identifiers

PMID28466149
OpenAlexW2611883831

What OpenQuestion holds

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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.