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用于预测横纹肌溶解症患者预后的可解释多任务模型的开发与验证:一项多中心回顾性队列研究

Development and validation of an interpretable multi-task model to predict outcomes in patients with rhabdomyolysis: a multicenter retrospective cohort study.

作者信息

Liu Chunli, Shi Jie, Wang Fengjuan, Li Duo, Luo Yu, Yang Bofan, Zhao Yunlong, Zhang Li, Yang Dingwei, Jin Heng, Song Jie, Guo Xiaoqin, Fan Haojun, Lv Qi

机构信息

School of Disaster and Emergency Medicine, Tianjin University, Tianjin, China.

Department of Nephrology, National Key Laboratory of Kidney Diseases, National Clinical Research Center for Kidney Diseases, Military Logistics Research Key Laboratory of Field Disease Treatment, Beijing Key Laboratory of Kidney Disease Research, First Medical Center of Chinese PLA General Hospital, Beijing, China.

出版信息

EClinicalMedicine. 2025 Aug 21;87:103438. doi: 10.1016/j.eclinm.2025.103438. eCollection 2025 Sep.

DOI:10.1016/j.eclinm.2025.103438
PMID:40896465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12396465/
Abstract

BACKGROUND

Rhabdomyolysis (RM) is a complex clinical syndrome with heterogeneous progression patterns among patients of varying severity. Early and accurate prediction of acute kidney injury (AKI), disease severity, renal replacement therapy (RRT) requirements, and mortality risk is essential for timely identification of high-risk individuals, personalized treatment planning, and optimal allocation of healthcare resources. We aimed to develop and externally validate an interpretable multi-task machine learning (ML) model to predict four clinical outcomes in patients with rhabdomyolysis: AKI, disease severity, the need for RRT, and in-hospital mortality.

METHODS

We conducted a retrospective study using three data sources: the eICU Collaborative Research Database (eICU-CRD), the Medical Information Mart for Intensive Care IV (MIMIC-IV), and electronic medical records from four tertiary hospitals in China. Data from eICU-CRD and MIMIC-IV were combined to form the derivation cohort for model training and internal validation, while data from the Chinese hospitals served as the external validation cohort. We analyzed 1429 patients from 2008 to 2019 in the derivation cohort and 362 patients from 2016 to 2022 in the external validation cohort. AKI was defined according to the Kidney Disease: Improving Global Outcomes (KDIGO) criteria, based on serum creatinine levels and urine output. Twenty-two clinical features available within the first 24 h of admission were selected to develop the prediction models. Ten machine learning (ML) algorithms were applied to construct multi-task prediction models. Model performance was evaluated using the area under the receiver operating characteristic curve (AUC). To improve interpretability, feature importance was assessed using the SHapley Additive exPlanation (SHAP) method.

FINDINGS

1429 patients were included in the derivation cohort (69.4% developed AKI, 36.7% were classified as having severe disease, 12.1% required RRT, and 9.8% had in-hospital mortality). 362 patients were included in the external validation cohort (27.9% developed AKI, 25.7% had severe disease, 27.3% required RRT, and 4.1% had in-hospital mortality). Among all evaluated models, the random forest (RF) algorithm exhibited the highest overall discriminative performance across the four prediction tasks. Based on feature importance rankings, interpretable final models were developed for each task using the top five contributing features. These models demonstrated robust predictive accuracy for AKI, disease severity, RRT requirements, and in-hospital mortality, with AUCs and corresponding 95% confidence intervals (CIs) of 0.914 (0.875-0.944), 0.909 (0.869-0.940), 0.888 (0.844-0.921), and 0.823 (0.773-0.865) in the internal validation cohort, and 0.906 (0.871-0.934), 0.856 (0.815-0.890), 0.852 (0.811-0.887), and 0.832 (0.789-0.869) in the external validation cohort, respectively. To support clinical implementation, a web- and Android-based decision support system was developed and is currently undergoing pilot testing in multiple hospitals.

INTERPRETATION

We developed and validated an interpretable multi-task ML model capable of accurately predicting key clinical outcomes in patients with RM. To improve clinical applicability, a user-friendly decision support system was implemented, incorporating interactive features to support frontline healthcare providers in real-time risk stratification and individualized management of RM.

FUNDING

National Key Research and Development Program of China (Nos. 2021YFC3002202 and 2023YFF1204104).

摘要

背景

横纹肌溶解症(RM)是一种复杂的临床综合征,在不同严重程度的患者中具有异质性进展模式。早期准确预测急性肾损伤(AKI)、疾病严重程度、肾脏替代治疗(RRT)需求和死亡风险对于及时识别高危个体、制定个性化治疗方案以及优化医疗资源分配至关重要。我们旨在开发并外部验证一个可解释的多任务机器学习(ML)模型,以预测横纹肌溶解症患者的四种临床结局:AKI、疾病严重程度、RRT需求和院内死亡率。

方法

我们使用三个数据源进行了一项回顾性研究:电子重症监护病房协作研究数据库(eICU-CRD)、重症监护医学信息集市IV(MIMIC-IV)以及中国四家三级医院的电子病历。来自eICU-CRD和MIMIC-IV的数据合并形成用于模型训练和内部验证的推导队列,而来自中国医院的数据作为外部验证队列。我们分析了推导队列中2008年至2019年的1429例患者以及外部验证队列中2016年至2022年的362例患者。AKI根据肾脏病:改善全球预后(KDIGO)标准,基于血清肌酐水平和尿量来定义。选择入院后24小时内可用的22项临床特征来开发预测模型。应用十种机器学习(ML)算法构建多任务预测模型。使用受试者操作特征曲线下面积(AUC)评估模型性能。为提高可解释性,使用SHapley加法解释(SHAP)方法评估特征重要性。

结果

推导队列纳入1429例患者(69.4%发生AKI,36.7%被分类为患有严重疾病,12.1%需要RRT,9.8%有院内死亡)。外部验证队列纳入362例患者(27.9%发生AKI,25.7%患有严重疾病,27.3%需要RRT,4.1%有院内死亡)。在所有评估模型中,随机森林(RF)算法在四项预测任务中总体判别性能最高。基于特征重要性排名,使用前五项贡献特征为每个任务开发了可解释的最终模型。这些模型在内部验证队列中对AKI、疾病严重程度、RRT需求和院内死亡率显示出强大的预测准确性,AUC及相应的95%置信区间(CI)分别为0.914(0.875 - 0.944)、0.909(0.869 - 0.940)、0.888(0.844 - 0.921)和0.823(0.773 - 0.865),在外部验证队列中分别为0.906(0.871 - 0.934)、0.856(0.815 - 0.890)、0.852(0.811 - 0.887)和0.832(0.789 - 0.869)。为支持临床应用,开发了一个基于网络和安卓的决策支持系统,目前正在多家医院进行试点测试。

解读

我们开发并验证了一个可解释的多任务ML模型,能够准确预测RM患者的关键临床结局。为提高临床适用性,实施了一个用户友好的决策支持系统,纳入交互式功能以支持一线医疗保健提供者对RM进行实时风险分层和个体化管理。

资助

中国国家重点研发计划(编号2021YFC3002202和2023YFF1204104)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7eb/12396465/3ac5115375b8/gr6.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7eb/12396465/7affc8f89cc7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7eb/12396465/1ef0cba00235/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7eb/12396465/9a7a8bb33782/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7eb/12396465/8b5140bb05ea/gr4.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7eb/12396465/3ac5115375b8/gr6.jpg

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