Evidence map›Paper›PMID 39806409›Full record

ArticleJournal of translational medicine2025

Establishment and validation of predictive model of ARDS in critically ill patients.

Senhao Wei, Hua Zhang, Hao Li, Chao Li, Ziyuan Shen, Yiyuan Yin, Zhukai Cong, Zhaojin Zeng, Qinggang Ge, Dongfeng Li and 1 more

Abstract readValidation Study
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

11 authors.

Senhao Wei *Department of Critical Care Medicine, Peking University Third Hospital, Beijing, 100191, China.
Hua Zhang *Clinical Epidemiology Research Center, Peking University Third Hospital, Beijing, 100191, China.
Hao Li *Department of Critical Care Medicine, Fuyang People's Hospital, Fuyang, 236000, China.
Chao Li *Department of Critical Care Medicine, Peking University Third Hospital, Beijing, 100191, China.
Ziyuan ShenDepartment of Critical Care Medicine, Peking University Third Hospital, Beijing, 100191, China.
Yiyuan YinDepartment of Critical Care Medicine, Peking University Third Hospital, Beijing, 100191, China.
Zhukai CongDepartment of Critical Care Medicine, Peking University Third Hospital, Beijing, 100191, China.
Zhaojin ZengDepartment of Critical Care Medicine, Peking University Third Hospital, Beijing, 100191, China.
Qinggang GeDepartment of Critical Care Medicine, Peking University Third Hospital, Beijing, 100191, China. qingganggelin@126.com.
Dongfeng LiDepartment of Critical Care Medicine, Fuyang People's Hospital, Fuyang, 236000, China. fylidongfeng@163.com.
Xi ZhuDepartment of Critical Care Medicine, Peking University Third Hospital, Beijing, 100191, China. xizhuccm@163.com.ORCID 0000-0001-6091-8831

Funding

Beijing Municipal Natural Science Foundation 7212130Capital Health Research and Development of Special Fund 20202-4094National Natural Science Foundation of China 82172166Peking University Third Hospital Cohort Study Project BYSYDL2021010Peking University Third Hospital Cohort Study Project BYSYZD2023012
6 · The paper itself

Abstract

backgroundAcute respiratory distress syndrome (ARDS) is a prevalent complication among critically ill patients, constituting around 10% of intensive care unit (ICU) admissions and mortality rates ranging from 35 to 46%. Hence, early recognition and prediction of ARDS are crucial for the timely administration of targeted treatment. However, ARDS is frequently underdiagnosed or delayed, and its heterogeneity diminishes the clinical utility of ARDS biomarkers. This study aimed to observe the incidence of ARDS among high-risk patients and develop and validate an ARDS prediction model using machine learning (ML) techniques based on clinical parameters.

methodsThis prospective cohort study in China was conducted on critically ill patients to derivate and validate the prediction model. The derivation cohort, consisting of 400 patients admitted to the ICU of the Peking University Third Hospital(PUTH) between December 2020 and August 2023, was separated for training and internal validation, and an external data set of 160 patients at the FU YANG People's Hospital from August 2022 to August 2023 was employed for external validation. Least absolute shrinkage and selection operator (LASSO) and multivariate logistic regression were used to screen predictor variables. Multiple ML classification models were integrated to analyze and identify the best models. Several evaluation indexes were used to compare the model performance, including the area under the receiver-operating-characteristic curve (AUC) and decision curve analysis (DCA). SHapley Additive ex Planations (SHAP) is used to interpret ML models.

results400 critically ill patients were included in the analysis, with 117 developing ARDS during follow-up. The final model included gender, Lung Injury Prediction Score (LIPS), Hepatic Disease, Shock, and combined Lung Contusion. Based on the AUC and DCA in the validation group, the logistic model demonstrated excellent performance, achieving an AUC of 0.836 (95% CI: 0.762-0.910). For external validation, comprising 160 patients, 44 of whom developed ARDS, the AUC was 0.799 (95% CI: 0.723-0.875), significantly outperforming the LIPS score alone.

conclusionCombining the LIPS score with other clinical parameters in a logistic regression model provides a more accurate, clinically applicable, and user-friendly ARDS prediction tool than the LIPS score alone.

Indexed as

Critical IllnessRespiratory Distress SyndromeAgedFemaleHumansIntensive Care UnitsLogistic ModelsMachine LearningMaleMiddle AgedProspective StudiesReproducibility of ResultsROC CurveARDSIntensive care unitLung injury prediction scorePrediction model

Identifiers

PMID39806409
PMCPMC11730794

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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.