Evidence map›Paper›PMID 40399915›Full record

ArticleBMC infectious diseases2025

Development of a risk prediction model for secondary infection in severe/critical COVID-19 patients.

Yinmei Zhang, Mingmei Lin, Zhenchao Wu, Zhongyu Han, Liyan Cui, Jiajia Zheng

Abstract read
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

6 authors.

Yinmei Zhang *Department of Laboratory Medicine, Peking University Third Hospital, Haidian District, No. 49 North Garden Road, Beijing, 100191, People's Republic of China.
Mingmei Lin *Department of Obstetrics and Gynecology, Peking University Third Hospital, Haidian District, No. 49 North Garden Road, Beijing, 100191, People's Republic of China.
Zhenchao WuDepartment of Respiratory and Critical Care Medicine, Peking University Third Hospital, Haidian District, No. 49 North Garden Road, Beijing, 100191, People's Republic of China.
Zhongyu HanDepartment of Laboratory Medicine, Peking University Third Hospital, Haidian District, No. 49 North Garden Road, Beijing, 100191, People's Republic of China.
Liyan CuiDepartment of Laboratory Medicine, Peking University Third Hospital, Haidian District, No. 49 North Garden Road, Beijing, 100191, People's Republic of China. cliyan@163.com.
Jiajia ZhengDepartment of Laboratory Medicine, Peking University Third Hospital, Haidian District, No. 49 North Garden Road, Beijing, 100191, People's Republic of China. zhengjiajia@bjmu.edu.cn.

Funding

Innovation & Transfer Fund of Peking University Third Hospital BYSYZHKC2022114Joint Laboratory of Medicine and Chemistry at Peking University Thrid Hospital BYSYJC2023005National Key Research and Development Program of China YFC2303203-02project for Beijing Haidian District Health Development Research and Cultivation Plan HP2024-30-501002
6 · The paper itself

Abstract

objectiveThis study aimed to develop a predictive model for secondary infections in patients with severe or critical COVID-19 by analyzing clinical characteristics and laboratory indicators.

methodA total of 307 patients with severe or critical COVID-19 admitted to Peking University Third Hospital from December 2022 to February 2023 were retrospectively analyzed, including 156 patients with secondary infection and 151 patients without secondary infection. The Boruta algorithm identified significant variables, and eight machine learning models were evaluated based on area under the curve (AUC) performance. The optimal model selected was further assessed, with model interpretability provided using SHapley Additive exPlanations (SHAP).

resultNine predictive factors were identified: Mechanical Ventilation, Procalcitonin (PCT), Interleukin-8 (IL-8), Interleukin-6 (IL-6), Blood Urea Nitrogen, Glucose, Creatine Kinase, Lactate Dehydrogenase, and Mean Platelet Volume (MPV). The random forest model demonstrated the best performance, with further evaluation showing an average AUC of 0.981 (CI 0.965-0.998) on the training set and 0.836 (CI 0.761-0.912) on the test set. SHAP analysis identified MPV, PCT, and IL-8 as the strongest predictors of secondary infections.

conclusionWe developed an effective predictive model for secondary infection risk in severe COVID-19 patients using readily available clinical parameters, enabling early clinical intervention. This machine learning approach demonstrates potential for improving patient management. CLINICAL TRIAL: This study does not involve clinical trial interventions. Therefore, clinical trial registration was not applicable.

Indexed as

CoinfectionCOVID-19AdultAgedCritical IllnessFemaleHumansInterleukin-8Machine LearningMaleMiddle AgedProcalcitoninRespiration, ArtificialRetrospective StudiesRisk AssessmentRisk FactorsInterleukin-8ProcalcitoninLaboratory indicatorsMachine learningRisk prediction modelSecondary infectionsSevere/critical COVID-19

Identifiers

PMID40399915
PMCPMC12096510

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.