Evidence map›Paper›PMID 39589673›Full record

ArticleAnnals of intensive care2024

Early reduction in gut microbiota diversity in critically ill patients is associated with mortality.

Hannah Wozniak, Nadia Gaïa, Vladimir Lazarevic, Christophe Le Terrier, Tal Sarah Beckmann, Eleonora Balzani, Martin Urner, Jérôme Pugin, Jacques Schrenzel, Claudia-Paula Heidegger and 1 more

Abstract read
In one paragraph

Article in Annals of intensive care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 3 pooled it
–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

13 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  4. Review
  5. The intestinal microbiota impacts nutritional immunity and resistance toProceedings of the National Academy of Sciences of the United States of America · 2026
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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

11 authors.

Hannah WozniakIntensive Care Unit, Department of Acute Medicine, Geneva University Hospitals, Geneva, Switzerland. hannah.wozniak@hug.ch.ORCID http://orcid.org/0000-0001-5404-4621
Nadia Gaïa *Genomic Research Laboratory, Department of Medicine, Geneva University, Geneva, Switzerland.
Vladimir Lazarevic *Genomic Research Laboratory, Department of Medicine, Geneva University, Geneva, Switzerland.
Christophe Le TerrierIntensive Care Unit, Department of Acute Medicine, Geneva University Hospitals, Geneva, Switzerland.
Tal Sarah BeckmannIntensive Care Unit, Department of Acute Medicine, Geneva University Hospitals, Geneva, Switzerland.
Eleonora BalzaniInterdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, Canada.
Martin UrnerInterdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, Canada.
Jérôme PuginIntensive Care Unit, Department of Acute Medicine, Geneva University Hospitals, Geneva, Switzerland.
Jacques Schrenzel *Genomic Research Laboratory, Department of Medicine, Geneva University, Geneva, Switzerland.
Claudia-Paula Heidegger *Intensive Care Unit, Department of Acute Medicine, Geneva University Hospitals, Geneva, Switzerland.
Gut Microbiota working group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCritical illness is associated with an altered gut microbiota, yet its association with poor outcomes remains unclear. This study evaluates the early gut microbiota diversity changes in intensive care unit patients and its association with mortality. Additionally, it explores fecal pH as a potential biomarker for these changes.

methodsIn this prospective observational cohort study, fecal samples were collected at two time points: S1, the first stool passed upon intensive care unit admission, and S2, the first stool passed at least 24 h after S1. Full-length 16S rRNA gene sequencing was performed for gut microbiota analysis, with α-diversity measured using the Shannon index. Bayesian joint models were used to estimate the association between time-varying changes in gut microbiota diversity and 60-day mortality, as well as the association between daily changes in stool pH and in diversity.

resultsTwenty-four of 96 patients overall died during follow-up. Daily Shannon index decreased on average by -0.1 points [95% Credible Intervals (CrI) -0.20 to -0.10]. Every point decrease in Shannon index was associated with a 1.99-fold increase in the hazard of death (95% CrI, 1.04 to 4.51). Time-varying fecal pH levels were not associated with changes in Shannon index.

conclusionsGut microbiota diversity decreased over time, associated with increased mortality. Fecal pH is an unreliable marker of gut microbiota change. Future studies on gut microbiota and related biomarkers should focus on the initial days in the intensive care unit to detect and mitigate a decline in gut microbiota diversity.

Indexed as

Critical careGut microbiotaPatients’ outcome

Identifiers

PMID39589673
PMCPMC11599525

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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.