Evidence map›Paper›PMID 40692680›Full record

ArticleFrontiers in cellular and infection microbiology2025

Development and validation of a multidimensional predictive model for 28-day mortality in ICU patients with bloodstream infections: a cohort study.

Jun Jin, Lei Yu, Qingshan Zhou, Qian Du, Xiangrong Nie, Hai-Yan Yin, Wan-Jie Gu

Abstract readValidation Study
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. 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.

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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

7 authors.

Jun Jin *Department of Intensive Care Unit, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Lei Yu *Department of Intensive Care Unit, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Qingshan ZhouDepartment of Intensive Care Unit, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Qian DuDepartment of Intensive Care Unit, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Xiangrong NieDepartment of Intensive Care Unit, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Hai-Yan YinDepartment of Intensive Care Unit, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Wan-Jie GuDepartment of Intensive Care Unit, The First Affiliated Hospital of Jinan University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bloodstream infections (BSI) are a leading cause of sepsis and death in intensive care unit (ICU). Traditional severity scores, including the Sequential Organ Failure Assessment (SOFA), Acute Physiology Score III (APSIII), and Simplified Acute Physiology Score II (SAPS II), exhibit limitations in effectively predicting mortality among BSI patients, primarily due to their reliance on a narrow range of clinical variables. This study aimed to develop and validate a comprehensive nomogram model for 28-day all-cause mortality prediction in BSI patients. Methods: A retrospective cohort study was conducted using data from 3,615 patients with positive blood cultures from the MIMIC-IV database, divided into training (n=2,532) and validation (n=1,083) cohorts. Through a two-step variable selection process combining LASSO regression and Boruta algorithm, we identified 12 predictive variables from 58 initial clinical parameters. The model's performance was evaluated using AUROC, net reclassification improvement (NRI), integrated discrimination improvement (IDI), and decision curve analysis (DCA). Results: The nomogram demonstrated superior discrimination (AUROC: 0.760 Conclusions: This study developed and validated a predictive model for 28-day mortality in BSI patients that demonstrated superior performance compared to traditional severity scores. By integrating clinical, laboratory, and treatment-related variables, the model provides a more comprehensive approach to risk stratification. These findings highlight its potential for improving early identification of high-risk patients and guiding clinical decision-making, though further prospective validation is needed to confirm its generalizability.

Indexed as

BacteremiaIntensive Care UnitsSepsisAgedCohort StudiesFemaleHumansMaleMiddle AgedNomogramsOrgan Dysfunction ScoresPrognosisRetrospective StudiesSeverity of Illness Index28-day all-cause mortalitybloodstream infectionsintensive care unitMIMIC-IV databasenomogrampredictive modelsepsis

Identifiers

PMID40692680
PMCPMC12277296

What Socratic holds

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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 Socratic graph.