Evidence map›Paper›PMID 39219264›Full record

ArticleVirulence2024

Simulating the clinical manifestations and disease progression of human sepsis: A monobacterial injection approach for animal modeling.

Xuanwen Ru, Simiao Chen, Danlei Chen, Qingyi Shao, Wenxia Shao, Qing Ye

Abstract read
In one paragraph

Article in Virulence, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
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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

6 authors.

Xuanwen RuDepartment of Clinical Laboratory, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID 0009-0002-7870-2515
Simiao ChenDepartment of Clinical Laboratory, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Danlei ChenSchool of Medical Technology and Information Engineering, Zhejiang Chinese Medical University, Hangzhou, China.
Qingyi ShaoSchool of Medical Technology and Information Engineering, Zhejiang Chinese Medical University, Hangzhou, China.
Wenxia ShaoHangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Qing YeDepartment of Clinical Laboratory, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID 0000-0002-6756-0630

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is defined as life-threatening organ dysfunction caused by a dysregulated host response to infection, with great clinical heterogeneity, high morbidity, and high mortality. At the same time, there are many kinds of infection sources, the pathophysiology is very complex, and the pathogenesis has not been fully elucidated. An ideal animal model of sepsis can accurately simulate clinical sepsis and promote the development of sepsis-related pathogenesis, treatment methods, and prognosis. The existing sepsis model still uses the previous Sepsis 2.0 modelling standard, which has some problems, such as many kinds of infection sources, poor repeatability, inability to take into account single-factor studies, and large differences from clinical sepsis patients. To solve these problems, this study established a new animal model of sepsis. The model uses intravenous tail injection of a single bacterial strain, simplifying the complexity of multibacterial infection, and effectively solving the above problems.

Indexed as

Disease Models, AnimalDisease ProgressionSepsisAnimalsHumansInjections, IntravenousMiceanimal model of sepsisclinical translationmonobacterial infectionpathophysiologySepsis

Identifiers

PMID39219264
PMCPMC11370922

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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.