Evidence map›Paper›PMID 30205441›Full record

ReviewHealthcare (Basel, Switzerland)2018

Sepsis: Personalized Medicine Utilizing 'Omic' Technologies-A Paradigm Shift?

Theis Skovsgaard Itenov, Daniel D Murray, Jens Ulrik Stæhr Jensen

Abstract readReview
In one paragraph

Review in Healthcare (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. Observational
  3. Observational
  4. Article
  5. Article
  6. Neonatal Sepsis: A Comprehensive Review.Antibiotics (Basel, Switzerland) · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Omics of endothelial cell dysfunction in sepsis.Vascular biology (Bristol, England) · 2022
    Review
  16. Article
  17. Review
  18. Resolving trained immunity with systems biology.European journal of immunology · 2021
    Review
  19. Review
  20. Article
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

3 authors.

Theis Skovsgaard ItenovPERSIMUNE, Rigshospitalet, Copenhagen DK-2100, Denmark. theis.skovsgaard.itenov@regionh.dk.
Daniel D MurrayPERSIMUNE, Rigshospitalet, Copenhagen DK-2100, Denmark. daniel.dawson.murray@regionh.dk.ORCID 0000-0001-8501-8661
Jens Ulrik Stæhr JensenPERSIMUNE, Rigshospitalet, Copenhagen DK-2100, Denmark. jens.ulrik.jensen@regionh.dk.ORCID 0000-0003-4036-0521

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis has over the years proven a considerable challenge to physicians and researchers. Numerous pharmacological and non-pharmacological interventions have been tested in trials, but have unfortunately failed to improve the general prognosis. This has led to the speculation that the sepsis population may be too heterogeneous to be targeted with the traditional one treatment suits all' approach. Recent advances in genetic and biochemical analyses now allow genotyping and biochemical characterisation of large groups of patients via the 'omics' technologies. These new opportunities could lead to a paradigm shift in the approach to sepsis towards personalised treatments with interventions targeted towards specific pathophysiological mechanisms activated in the patient. In this article, we review the potentials and pitfalls of using new advanced technologies to deepen our understanding of the clinical syndrome of sepsis.

Indexed as

genomicsmetabolomicssepsissystems biologytranscriptomicstransitional research

Identifiers

PMID30205441
PMCPMC6163606

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.