Evidence map›Paper›PMID 40987007›Full record

ArticleShock (Augusta, Ga.)2026

Dynamic Multiorgan Dysfunction After Trauma With Secondary Sepsis in Rats: A 6-72-Hour Temporal Map Validated by Rodent-Specific Mods Scoring.

Baisheng Sun, Dongxu Qian, Cong Zhang, Ziwei Han, Zhi Mao, Feihu Zhou

Abstract read
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Article in Shock (Augusta, Ga.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Baisheng SunDepartment of Critical Care Medicine, the First Medical Centre, Chinese PLA General Hospital, Beijing, China.
Dongxu QianDepartment of Critical Care Medicine, the First Medical Centre, Chinese PLA General Hospital, Beijing, China.
Cong ZhangHealth Team of the 61172nd Troop of Chinese PLA, Beijing, China.
Ziwei HanDepartment of Critical Care Medicine, the First Medical Centre, Chinese PLA General Hospital, Beijing, China.
Zhi MaoDepartment of Critical Care Medicine, the First Medical Centre, Chinese PLA General Hospital, Beijing, China.
Feihu ZhouDepartment of Critical Care Medicine, the First Medical Centre, Chinese PLA General Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aimed to quantify the temporal evolution of multiple organ dysfunction syndrome (MODS) following trauma with secondary sepsis and to validate a rodent-specific MODS scoring system over 6-72 hours.

methodsA total of 168 male Sprague-Dawley rats (8 weeks old, SPF grade) were randomly divided into four groups: the normal control group (NC group), limb crush injury group (Fx group), cecal ligation and puncture group (CLP group), and limb crush injury combined with CLP group (Fx+CLP group). A stepwise CLP surgery was performed in the Fx+CLP group 24 hours after closed tibial and fibular fracture surgery to mimic the clinical window of high infection incidence. Five observation time points were set: 6, 12, 24, 48, and 72 hours. Hematological parameters were detected, and tissues of rats were examined histopathologically before a diagnostic scoring system for MODS in experimental animals was constructed.

resultsThe mortality rate of the Fx+CLP group was 58.33%, significantly higher than in the other groups ( P < 0.01). The levels of white blood cells, interleukin (IL)-6, and IL-10 in the Fx+CLP group, which peaked at 24 hours, were notably higher than those of the CLP group at each time point ( P < 0.01). During the organ-function assessment, the Fx+CLP group started to present with cardiac and hepatic dysfunction 12 hours after the first onset, and pulmonary and renal dysfunction 24 hours after the first onset. The pathological damage to the organs worsened with time. Particularly, the brain tissue pathology suggested that the pathological score of the Fx+CLP group exceeded 2 at 24 hours after the first onset. Moreover, coagulation dysfunction started 12 hours after the first onset. In general, the timing features of organ damage were distinct, and the overall damage was much more severe than in the single-factor damage groups.

conclusionsA consecutive 6- to -72-hour quantitative profile of MODS across six organ systems was established, demonstrating that cardiac and hepatic dysfunction emerged at 12 hours, followed by pulmonary, renal, neurological, and coagulatory failure at 24 hours. The validated MODS score was expected to offer a robust translational tool for timing therapeutic interventions.

Indexed as

Multiple Organ FailureSepsisWounds and InjuriesAnimalsDisease Models, AnimalInterleukin-10Interleukin-6MaleOrgan Dysfunction ScoresRatsRats, Sprague-DawleyTime FactorsInterleukin-10Interleukin-6Animal modelinflammatory responsemultiple organ dysfunction syndrome (MODS)organ injury assessmenttraumatic sepsis

Identifiers

PMID40987007
PMCPMC13313464

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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.