Huang Huai, Ren Guangqin, Sun Shanghui, Li Zhi, Zheng Yongtian, Dong Lijuan, Zhu Shaoliang, Zhu Xiaosheng, Jiang Wenyu
Department of Neurological Rehabilitation, Jiangbin Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Department of Anesthesiology, Zhongshan Hospital of Traditional Chinese Medicine Affiliated to Guangzhou University of Traditional Chinese Medicine, Zhongshan, China.
Front Pharmacol. 2025 Jan 7;15:1527664. doi: 10.3389/fphar.2024.1527664. eCollection 2024.
This study aims to evaluate the association between the white blood cell-to-platelet ratio (WPR) and 28-day all-cause mortality among patients experiencing cardiac arrest.
Utilizing data from 748 cardiac arrest patients in the Medical Information Mart for Intensive Care-IV (MIMIC-IV) 2.2 database, machine learning algorithms, including the Boruta feature selection method, random forest modeling, and SHAP value analysis, were applied to identify significant prognostic biomarkers. Key patient characteristics, encompassing demographic data, comorbidities, hematological and biochemical indices, and vital signs, were extracted using PostgreSQL Administration Tool (pgAdmin) software. The Cox proportional hazards model assessed the impact of WPR on mortality outcomes, while Kaplan-Meier survival curves and restricted cubic spline (RCS) analysis further validated the findings. Subgroup analyses stratified the prognostic value of WPR by demographic and clinical factors.
WPR demonstrated the highest prognostic significance among the variables studied, showing a strong association with 28-day all-cause mortality. In the unadjusted Model 1, hazard ratios (HRs) for WPR quartiles ranged from 1.88 (95% CI: 1.22-2.90) in Q2 to 3.02 (95% CI: 2.04-4.47) in Q4 (Ptrend <0.05). Adjusted models (Models 2-4) confirmed the robustness of these associations, even after accounting for demographic and clinical covariates. Kaplan-Meier and RCS analyses revealed a significant U-shaped relationship between WPR and mortality risk. Subgroup analyses indicated that elevated WPR was particularly associated with increased mortality in males, elderly patients, married individuals, and those with chronic pulmonary disease.
WPR serves as an independent and reliable prognostic biomarker for 28-day mortality in cardiac arrest patients. Its integration into clinical decision-making may enhance the early identification of high-risk patients and guide tailored therapeutic interventions.
本研究旨在评估心脏骤停患者的白细胞与血小板比值(WPR)与28天全因死亡率之间的关联。
利用重症监护医学信息集市-IV(MIMIC-IV)2.2数据库中748例心脏骤停患者的数据,应用机器学习算法,包括Boruta特征选择方法、随机森林建模和SHAP值分析,以识别重要的预后生物标志物。使用PostgreSQL管理工具(pgAdmin)软件提取关键患者特征,包括人口统计学数据、合并症、血液学和生化指标以及生命体征。Cox比例风险模型评估WPR对死亡率结局的影响,而Kaplan-Meier生存曲线和受限立方样条(RCS)分析进一步验证了研究结果。亚组分析按人口统计学和临床因素对WPR的预后价值进行分层。
在研究的变量中,WPR显示出最高的预后意义,与28天全因死亡率密切相关。在未调整的模型1中,WPR四分位数的风险比(HR)范围从第二四分位数的1.88(95%CI:1.22-2.90)到第四四分位数的3.02(95%CI:2.04-4.47)(P趋势<0.05)。调整后的模型(模型2-4)证实了这些关联的稳健性,即使在考虑了人口统计学和临床协变量之后。Kaplan-Meier和RCS分析揭示了WPR与死亡风险之间存在显著的U形关系。亚组分析表明,WPR升高尤其与男性、老年患者、已婚个体以及患有慢性肺病的患者死亡率增加相关。
WPR是心脏骤停患者28天死亡率的独立且可靠的预后生物标志物。将其纳入临床决策可能会增强对高危患者的早期识别,并指导针对性的治疗干预。