Wei Rao, Li Kexin, Wang Huaguang, Cai Xinbo, Liu Nian, An Zhuoling, Zhou Hong
Pharmacy Department of Beijing Chao-Yang Hospital, Capital Medical University, Beijing, People's Republic of China.
Hematology Department of Beijing Chao-Yang Hospital, Capital Medical University, Beijing, People's Republic of China.
Infect Drug Resist. 2025 May 23;18:2653-2661. doi: 10.2147/IDR.S479658. eCollection 2025.
Using artificial intelligence and machine learning to predict linezolid-induced thrombocytopenia helps identify related risk factors in patients.
Between January 2020 and December 2023, 284 patients receiving linezolid from Beijing Chaoyang Hospital were enrolled. The data underwent filtering to ensure completeness and quality. The filtered data were then randomly divided into training and validation sets at a 3:1 ratio using stratified sampling. Four machine learning methods-logistic regression, Lasso regression, support vector machine (SVM), and random forest-were employed to develop predictive models on the training set, with optimal hyperparameters determined through grid search. Model performance was assessed via 10 - fold cross - validation on the training set, and the model with the highest AUC was selected. The chosen model was further validated on the independent validation set, with AUC, sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) calculated.
During treatment with linezolid, 42 (14.8%) of the 284 patients developed thrombocytopenia, with an average onset of 12.0±5.6 days after starting linezolid therapy. The random forest model demonstrated the best performance, with an AUC of 0.902 (95% CI 0.814-0.991) in the validation set. This model achieved a sensitivity of 81.8%, specificity of 86.9%, positive predictive value (PPV) of 52.9%, and negative predictive value (NPV) of 96.4%.
We developed a machine learning model to predict linezolid-associated thrombocytopenia, with the random forest model achieving an AUC of 0.902. This model can help clinicians assess patient risk and optimize treatment plans. Future work should validate the model in multicenter studies and explore its integration into clinical decision support systems.
利用人工智能和机器学习预测利奈唑胺诱导的血小板减少症,有助于识别患者的相关风险因素。
2020年1月至2023年12月期间,纳入北京朝阳医院284例接受利奈唑胺治疗的患者。对数据进行筛选,以确保完整性和质量。然后使用分层抽样以3:1的比例将筛选后的数据随机分为训练集和验证集。采用逻辑回归、套索回归、支持向量机(SVM)和随机森林四种机器学习方法在训练集上建立预测模型,并通过网格搜索确定最佳超参数。通过在训练集上进行10倍交叉验证来评估模型性能,并选择AUC最高的模型。在独立验证集上对所选模型进行进一步验证,计算AUC、敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV)。
在利奈唑胺治疗期间,284例患者中有42例(14.8%)发生血小板减少症,利奈唑胺治疗开始后平均发病时间为12.0±5.6天。随机森林模型表现最佳,在验证集中AUC为0.902(95%CI 0.814-0.991)。该模型的敏感性为81.8%,特异性为86.9%,阳性预测值(PPV)为52.9%,阴性预测值(NPV)为96.4%。
我们开发了一种机器学习模型来预测利奈唑胺相关的血小板减少症,随机森林模型的AUC为0.902。该模型可帮助临床医生评估患者风险并优化治疗方案。未来的工作应在多中心研究中验证该模型,并探索将其整合到临床决策支持系统中。