Evidence map›Paper›PMID 32039976›Full record

Observational studyThe journal of trauma and acute care surgery2020

The gut microbiome distinguishes mortality in trauma patients upon admission to the emergency department.

David M Burmeister, Taylor R Johnson, Zhao Lai, Shannon R Scroggins, Mark DeRosa, Rachelle B Jonas, Caroline Zhu, Elizabeth Scherer, Ronald M Stewart, Martin G Schwacha and 3 more

Abstract readObservational Study
In one paragraph

Observational study in The journal of trauma and acute care surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Trial
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  5. Article
  6. Article
  7. New insights into metabolism dysregulation after TBI.Journal of neuroinflammation · 2024
    Review
  8. Radiation-induced multi-organ injury.International journal of radiation biology · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Review
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  14. Article
  15. Article
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  18. Stress-related changes in the gut microbiome after trauma.The journal of trauma and acute care surgery · 2021
    Article
  19. Review
  20. Review
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

13 authors.

David M BurmeisterFrom the Division of Trauma and Emergency Surgery, Department of Surgery (D.M.B., T.R.J., S.S., M.D., R.B.J., C.Z., E.S., R.M.S., M.G.S., D.H.J., B.J.E., S.E.N.), Greehey Children's Cancer Research Institute (Z.L.), and Department of Molecular Medicine (Z.L.), UT Health San Antonio, San Antonio, Texas; Department of Medicine, Uniformed Services University of the Health Sciences (D.M.B), Bethesda, MD and US Army Institute of Surgical Research (D.M.B., S.E.N.), Fort Sam Houston, Texas.
Taylor R Johnson
Zhao Lai
Shannon R Scroggins
Mark DeRosa
Rachelle B Jonas
Caroline Zhu
Elizabeth Scherer
Ronald M Stewart
Martin G Schwacha
Donald H Jenkins
Brian J Eastridge
Susannah E Nicholson

Funding

Institutional Career Development Core (KL2)KL2TR002646 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI TSEVAT, JOEL · 2018 to 2022
$3.4M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthKL2TR001118 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, DOUGHERTY, DONALD M · 2013 to 2017
$3.4M
NCATS NIH HHS KL2 TR001118NCATS NIH HHS KL2 TR002646
6 · The paper itself

Abstract

backgroundTraumatic injury can lead to a compromised intestinal epithelial barrier, decreased gut perfusion, and inflammation. While recent studies indicate that the gut microbiome (GM) is altered early following traumatic injury, the impact of GM changes on clinical outcomes remains unknown. Our objective of this follow-up study was to determine if the GM is associated with clinical outcomes in critically injured patients.

methodsWe conducted a prospective, observational study in adult patients (N = 67) sustaining severe injury admitted to a level I trauma center. Fecal specimens were collected on admission to the emergency department, and microbial DNA from all samples was analyzed using the Quantitative Insights Into Microbial Ecology pipeline and compared against the Greengenes database. α-Diversity and β-diversity were estimated using the observed species metrics and analyzed with t tests and permutational analysis of variance for overall significance, with post hoc pairwise analyses.

resultsOur patient population consisted of 63% males with a mean age of 44 years. Seventy-eight percent of the patients suffered blunt trauma with 22% undergoing penetrating injuries. The mean body mass index was 26.9 kg/m. Significant differences in admission β-diversity were noted by hospital length of stay, intensive care unit hospital length of stay, number of days on the ventilator, infections, and acute respiratory distress syndrome (p < 0.05). β-Diversity on admission differed in patients who died compared with patients who lived (mean time to death, 8 days). There were also significantly less operational taxonomic units in samples from patients who died versus those who survived. A number of species were enriched in the GM of injured patients who died, which included some traditionally probiotic species such as Akkermansia muciniphilia, Oxalobacter formigenes, and Eubacterium biforme (p < 0.05).

conclusionGut microbiome diversity on admission in severely injured patients is predictive of a variety of clinically important outcomes. While our study does not address causality, the GM of trauma patients may provide valuable diagnostic and therapeutic targets for the care of injured patients. LEVEL OF EVIDENCE: Prognostic and epidemiological, level III.

Indexed as

AdultAgedEmergency Service, HospitalFecesFemaleFollow-Up StudiesGastrointestinal MicrobiomeHospital MortalityHumansInjury Severity ScoreLength of StayMaleMiddle AgedPrognosisProspective StudiesTrauma Centers

Identifiers

PMID32039976
PMCPMC7905995

What OpenQuestion holds

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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.