Evidence map›Paper›PMID 42948031›Full record

ReviewMedComm2026

Sepsis: Epidemiology, Pathophysiology, and Management.

Guang-Tao Pan, Yu Deng, Lin-Rui Ma, Yu-Tong Li, Yu Qian, Yi-Hua Ma, Hai-Wei Rao, Yi-Zhun Zhu, Pei-Yu Yan

Abstract readReview
In one paragraph

Review in MedComm, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Guang-Tao Pan *Yancheng Hospital of Traditional Chinese Medicine Affiliated to Nanjing University of Chinese Medicine (Yancheng Hospital of Traditional Chinese Medicine) Yancheng Jiangsu China.
Yu Deng *Faculty of Chinese Medicine Macau University of Science and Technology Macau SAR China.
Lin-Rui MaFaculty of Chinese Medicine Macau University of Science and Technology Macau SAR China.
Yu-Tong LiFaculty of Chinese Medicine Macau University of Science and Technology Macau SAR China.
Yu QianFaculty of Chinese Medicine Macau University of Science and Technology Macau SAR China.
Yi-Hua MaFaculty of Chinese Medicine Macau University of Science and Technology Macau SAR China.
Hai-Wei RaoFaculty of Chinese Medicine Macau University of Science and Technology Macau SAR China.
Yi-Zhun ZhuSchool of Pharmacy Macau University of Science and Technology Macau SAR China.
Pei-Yu YanFaculty of Chinese Medicine State Key Laboratory of Mechanism and Quality of Chinese Medicine Macau University of Science and Technology Macau SAR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis remains a major cause of global morbidity and mortality despite advances in recognition, antimicrobial therapy, and organ support, reflecting its biological heterogeneity and the absence of broadly effective host-directed treatments. Here, we synthesize recent evidence across the three domains that define contemporary sepsis: epidemiology, pathophysiology, and management. Global and regional data indicate a persistently high but uneven burden, shaped by differences in case definitions, population structure, healthcare resources, and ascertainment. Mechanistically, sepsis is best viewed as an interconnected systems disorder in which hyperinflammation and immunoparalysis coexist with oxidative stress, endothelial and coagulation injury, immunometabolic dysfunction, gut dysbiosis, mitochondrial damage, and dysregulated programmed cell death, collectively driving organ dysfunction. Current management remains centered on timely antimicrobials, source control, individualized fluid and vasopressor therapy, corticosteroids, and organ support, while biomarker-guided immunotherapy and other host-directed strategies remain investigational. Recent randomized trials have mainly refined how established treatments are delivered rather than identified a universally effective new therapy. We also evaluate preclinical evidence for natural compounds targeting inflammatory and cell-death networks and highlight persistent methodological, pharmacokinetic, and translational barriers. Integrating rigorous phenotyping, mechanistic biomarkers, and guideline-based care may provide a more realistic path toward precision sepsis therapy.

Indexed as

epidemiologymanagementnatural compoundspathophysiologyprecision immunotherapyprogrammed cell deathsepsis

Identifiers

PMID42948031
PMCPMC13711029

What OpenQuestion holds

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Read underepoch 390

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.