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Soluble Thrombomodulin can Predict In-Hospital Mortality of Community-Acquired Pneumonia Patients in Intensive Care Unit

医学 重症监护室 内科学 逻辑回归 阿帕奇II 肺炎 生物标志物 急性肾损伤 肾脏疾病 曲线下面积 接收机工作特性 重症监护医学 降钙素原 回顾性队列研究 血栓调节蛋白 疾病 疾病严重程度 败血症 急诊医学 死亡风险 重症监护 试验预测值 切断 死亡率 社区获得性肺炎
作者
Yan Pan
出处
期刊:Clinical Laboratory [Clinical Laboratory Publications]
卷期号:72 (06/2026)
标识
DOI:10.7754/clin.lab.2025.251055
摘要

BACKGROUND: Community-acquired pneumonia (CAP) patients admitted to ICU face high mortality rates, necessitating prognostic biomarkers to risk stratify patients. Soluble thrombomodulin (sTM) is a biomarker of endothelial injury. This retrospective study aimed to investigate sTM's association with disease severity and in-hospital mortality in ICU-admitted CAP patients. METHODS: From June 2024 to September 2025, 115 ICU CAP patients in Shanghai Jian District Shibei Hospital were analyzed retrospectively. sTM levels were measured together with other laboratory tests at ICU admission. Demographic data, clinical characteristics, APACHE II scores and laboratory test results were obtained from medical records. The difference between 97 survivors and 18 non-survivors were compared. ROC analysis and multivariable logistic regression were used to evaluate sTM's value in predicting in-hospital mortality. Spearman's correlation and multiple linear regression assessed the association of sTM with other blood biomarkers and APECH II scores. RESULTS: Non-survivors had significantly higher sTM than survivors. sTM correlated with APACHE II scores and disease severity, as well as blood biomarkers of kidney function, inflammation and coagulation. ROC analysis showed that sTM predicted in-hospital mortality with an AUC of 0.747 (p < 0.001), higher than that of APACHE II score. The optimal cutoff of sTM was 12.9 TU/mL with sensitivity of 88.9% and specificity of 53.6%. Elevated sTM levels remained independently associated with the risk of in-hospital mortality even after adjusted with APACHE II scores or kidney dysfunction. CONCLUSIONS: sTM levels were significantly higher in non-survivors and correlates to APACHE II scores, suggesting its potential as a prognostic biomarker, aiding early risk stratification and tailored ICU management for CAP patients.
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