Evidence map›Paper›PMID 42094972›Full record

ArticleFrontiers in medicine2026

Systemic inflammatory indices and 28-day mortality in severe pneumonia: a retrospective single-center exploratory study.

Xingxing Chen, Weiqiang Huang, Wenjing Dai, Wei Zhang, Xiaofeng Zhong, Ming Hu

Abstract read
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Article in Frontiers in medicine, 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.

Xingxing Chen *Intensive Care Unit, Wuhan Pulmonary Hospital, Wuhan, Hubei, China.
Weiqiang Huang *Intensive Care Unit, Wuhan Pulmonary Hospital, Wuhan, Hubei, China.
Wenjing DaiIntensive Care Unit, Wuhan Pulmonary Hospital, Wuhan, Hubei, China.
Wei ZhangIntensive Care Unit, Wuhan Pulmonary Hospital, Wuhan, Hubei, China.
Xiaofeng ZhongIntensive Care Unit, Wuhan Pulmonary Hospital, Wuhan, Hubei, China.
Ming HuIntensive Care Unit, Wuhan Pulmonary Hospital, Wuhan, Hubei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Severe pneumonia remains a major cause of intensive care unit admission and death, and practical tools for early risk stratification remain limited. We evaluated several readily available systemic inflammatory indices and their association with 28-day all-cause mortality in patients with severe pneumonia. Methods: This retrospective single-center study included 100 ICU patients with severe pneumonia treated between January 2022 and December 2023. The primary endpoint was 28-day all-cause mortality. Patients were classified into a death group ( Results: Several inflammatory indices were higher in patients who died within 28 days. In unadjusted and minimally adjusted analyses, SIRI, NLR, and IBI were significantly associated with 28-day mortality. After further adjustment for age, sex, body mass index, smoking, drinking, admission APACHE II score, oxygenation index, mechanical ventilation duration, and major baseline comorbidities, only SIRI and NLR remained independently associated with 28-day mortality. In the fully adjusted model, each 1-standard deviation increase in SIRI and NLR was associated with higher odds of 28-day death (SIRI: OR 2.16, 95% CI 1.08-4.33; NLR: OR 2.12, 95% CI 1.14-3.95). By contrast, the associations of SII and IBI were attenuated after additional adjustment, and PLR was not independently associated with 28-day mortality. Conclusion: Among the evaluated inflammatory indices, SIRI and NLR showed the most stable independent associations with 28-day all-cause mortality in severe pneumonia. These findings are exploratory and require external validation, but they suggest that selected inflammation-based indices may provide additional prognostic information beyond conventional severity markers.

Indexed as

immune-inflammatory biomarkersinflammation-based indexintensive care unitprognostic modelrisk stratificationsevere pneumonia

Identifiers

PMID42094972
PMCPMC13139138

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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.