Evidence map›Paper›PMID 41620611›Full record

ArticleBMC infectious diseases2026

Toward precision risk stratification: predicting in-hospital death in sepsis patients with MRSA bacteremia.

Linmu Chen, Yunxiu Huang, Weiguo Zhao

Abstract read
In one paragraph

Article in BMC infectious diseases, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

3 authors.

Linmu ChenDepartment of Pharmacy of Zhongshan City People's Hospital, Zhongshan, Guangdong Province, 528403, China.
Yunxiu HuangDepartment of Laboratory Medicine of Zhongshan City People's Hospital, Zhongshan, Guangdong Province, 528403, China.
Weiguo ZhaoDepartment of Pharmacy of Zhongshan City People's Hospital, Zhongshan, Guangdong Province, 528403, China. zwgbaby@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with sepsis and concurrent methicillin-resistant Staphylococcus aureus (MRSA) bloodstream infection face a substantial risk of mortality. This study aimed to develop and validate a pragmatic, interpretable prediction model for in-hospital mortality in this high-risk population. We conducted a retrospective, single-center cohort study including 1,605 eligible patients, who were randomly divided into a training set (n = 1,124) and a validation set (n = 481). A rigorous, multi-stage feature selection pipeline—integrating univariate analysis, multi-model machine learning importance assessment, the Boruta algorithm, and stability selection via LASSO—was applied to 64 candidate variables. This process identified seven parsimonious, clinically accessible predictors: Glasgow Coma Scale score, minimum pH, maximum blood urea nitrogen, minimum white blood cell count, minimum platelet count, maximum lactate level, and the presence of pneumonia. Among six compared machine learning algorithms, logistic regression was selected for its optimal balance of performance and inherent interpretability. The final model demonstrated strong discriminative ability, with an area under the receiver operating characteristic curve (AUC) of 0.861 (95% CI: 0.840–0.882) in the training set and 0.844 (95% CI: 0.811–0.877) in the independent validation set, and showed good calibration (Hosmer-Lemeshow test p = 0.274). Decision curve analysis confirmed superior clinical net benefit across a wide range of risk thresholds. The model maintained robust and equitable performance across key patient subgroups and exhibited stability in extensive sensitivity analyses, including multiple imputation and bootstrap internal validation. This interpretable, seven-variable logistic regression model provides a clinically actionable tool for early mortality risk stratification, potentially supporting timely and tailored intervention strategies for sepsis patients with MRSA bacteremia.

Indexed as

BacteremiaHospital MortalityMethicillin-Resistant Staphylococcus aureusSepsisStaphylococcal InfectionsAgedAged, 80 and overFemaleHumansLogistic ModelsMachine LearningMaleMiddle AgedRetrospective StudiesRisk AssessmentROC CurveMortalityMRSAPredictive modelRisk stratificationSepsis

Identifiers

PMID41620611
PMCPMC12934007

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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.