The Value of Heparin Binding Protein in Early Identification of Sepsis-Induced Coagulopathy Disease and Prognosis.

IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY
Daorong Wu, Tingyu Wen, Fan Li, Zhixiang Wanyan, Zihao Ma, Peng Ji, Shujun Guo, Rui Li, Ming Xue, Kaijun Fen, Qiuming Song
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引用次数: 0

Abstract

Background: The aim of this study was to explore the value of heparin-binding protein (HBP) in the early recognition of sepsis coagulopathy (SIC) and the prognosis of sepsis patients.

Methods: A retrospective analysis was performed for 139 patients with sepsis admitted to the Intensive Care Unit (ICU) of Hefei Third People's Hospital from April 2022 through April 2024. The clinical baseline data, disease scores [sequential organ failure (SOFA) score, acute physiology and chronic health status (APACHE II) score, and SIC score], inflammatory markers [HBP, procalcitonin (PCT), and interleukin 6 (IL-6)], coagulation-related indexes [platelet count (PLT), prothrombin time (PT), prothrombin time international normalized ratio (PT-INR), activated partial thromboplastin time (APTT), fibrinogen (Fib), and D dimer (D-D)], and the survival time and 28-day prognosis of all patients were observed. The correlation between HBP and disease scores, inflammatory indexes, and coagulation-related indexes was analyzed. The receiver operating characteristic (ROC) curve was used to analyze the predictive value of HBP for SIC and the value of HBP and SIC score for the prognosis of sepsis, the risk stratification was carried out according to the optimal cutoff value of HBP, the differences in the occurrence of major clinical events under different HBP stratifications were compared, and the Kaplan-Meier survival curve was used to analyze the 28-day cumulative survival rate under different HBP stratifications.

Results: Among the 139 patients, 98 developed SIC, 41 did not, 73 died at 28 days, and 66 survived. The disease score, inflammation index, and coagulation-related indexes of the non-SIC group were better than those of the SIC group, and the disease scores, inflammation indexes, and coagulation-related indexes of the survival group were better than those of the death group. Correlation analysis showed that HBP was positively correlated with disease score and inflammation index. Coagulation-related index was positively correlated with PT, APTT, PT-INR, Fib, and D-D, and negatively correlated with PLT, among which HBP had the best correlation with disease score (HBP was best correlated with SIC, SOFA, and APACHE II scores; r = 0.818, 0.847, and 0.829, p < 0.001). ROC analysis showed that HBP had a high efficacy in identifying SIC (AUC = 0.934, sensitivity 96.9%, specificity 87.8%, p < 0.001), and the AUC of HBP and SIC score and their combination for 28-day death prediction were 0.802, 0.773, and 0.844 (p < 0.001), respectively. Compared with the HBP ≤ 118.25 ng/mL group (n = 52), the 28-day mortality rate, SIC incidence, APACHE II, and SOFA scores were higher in the HBP > 118.25 ng/mL group (n = 52) (p < 0.001). Kaplan-Meier survival curve analysis showed that the cumulative survival rate of the HBP > 118.25 ng/mL group was significantly lower than that of the HBP ≤ 118.25 ng/mL group (p < 0.001).

Conclusions: HBP has a high predictive value in the early identification of SIC and the prognosis evaluation of sepsis, and patients with sepsis with an early HBP > 118.25 ng/mL in the ICU have a higher risk of SIC and death.

肝素结合蛋白在脓毒症致凝血病早期诊断及预后中的价值。
背景:本研究旨在探讨肝素结合蛋白(HBP)在脓毒症凝血病(SIC)早期识别及脓毒症患者预后中的价值。方法:对合肥市第三人民医院重症监护病房(ICU) 2022年4月至2024年4月收治的139例脓毒症患者进行回顾性分析。临床基线数据、疾病评分[顺序性器官衰竭(SOFA)评分、急性生理和慢性健康状况(APACHE II)评分和SIC评分]、炎症标志物[HBP、降钙素原(PCT)和白细胞介素6 (IL-6)]、凝血相关指标[血小板计数(PLT)、凝血酶原时间(PT)、凝血酶原时间国际标准化比值(PT- inr)、活化部分凝血活素时间(APTT)、纤维蛋白原(Fib)和D-二聚体(D-D)]、观察患者的生存时间及28天预后。分析HBP与疾病评分、炎症指标、凝血相关指标的相关性。接受者操作特征曲线(ROC)被用来分析预测价值方面对碳化硅和HBP的价值和碳化硅为脓毒症的预后评分,根据最优风险分层进行了截断值方面,主要临床事件的发生的差异在不同HBP层次比较、和kaplan meier生存曲线用于分析不同HBP层次下的28天累积生存率。结果:139例患者中,98例发生SIC, 41例未发生SIC, 73例在28天死亡,66例存活。非SIC组的疾病评分、炎症指标、凝血相关指标优于SIC组,生存组的疾病评分、炎症指标、凝血相关指标优于死亡组。相关分析显示,HBP与疾病评分、炎症指数呈正相关。凝血相关指数与PT、APTT、PT- inr、Fib、D-D呈正相关,与PLT呈负相关,其中HBP与疾病评分相关性最好(HBP与SIC、SOFA、APACHE II评分相关性最好;R = 0.818, 0.847, 0.829, p < 0.001)。ROC分析显示,HBP对SIC有较高的识别效率(AUC = 0.934,敏感性96.9%,特异性87.8%,p < 0.001), HBP与SIC评分及其联合预测28天死亡的AUC分别为0.802、0.773、0.844 (p < 0.001)。与HBP≤118.25 ng/mL组(n = 52)相比,HBP≤118.25 ng/mL组(n = 52) 28天死亡率、SIC发生率、APACHE II和SOFA评分均较高(p < 0.001)。Kaplan-Meier生存曲线分析显示,HBP≥118.25 ng/mL组的累积生存率显著低于HBP≤118.25 ng/mL组(p < 0.001)。结论:HBP对SIC的早期识别和脓毒症的预后评价具有较高的预测价值,ICU中早期HBP > 118.25 ng/mL的脓毒症患者发生SIC及死亡的风险较高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical laboratory
Clinical laboratory 医学-医学实验技术
CiteScore
1.50
自引率
0.00%
发文量
494
审稿时长
3 months
期刊介绍: Clinical Laboratory is an international fully peer-reviewed journal covering all aspects of laboratory medicine and transfusion medicine. In addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies. The journal publishes original articles, review articles, posters, short reports, case studies and letters to the editor dealing with 1) the scientific background, implementation and diagnostic significance of laboratory methods employed in hospitals, blood banks and physicians'' offices and with 2) scientific, administrative and clinical aspects of transfusion medicine and 3) in addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies.
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