Jin Yude, Fei Liping
Department of General Surgery, First Affiliated Hospital of Huzhou University Huzhou 313000, Zhejiang, China.
Department of Intensive Care Unit, First Affiliated Hospital of Huzhou University Huzhou 313000, Zhejiang, China.
Am J Transl Res. 2025 Aug 15;17(8):6381-6390. doi: 10.62347/ZZBC1816. eCollection 2025.
To investigate the role of coagulation biomarkers (fibrinogen [FIB], fibrin degradation products [FDP], D-dimer [D-D], FDP/FIB ratio) in predicting transfusion outcomes in trauma patients.
A retrospective analysis of 112 trauma cases (May 2020-May 2024) stratified into good (n=80) and poor prognosis (n=32) groups based on transfusion outcomes was conducted. Pre-transfusion levels of coagulation biomarkers were compared between groups. Pearson correlation assessed associations among markers, and logistic regression identified outcome predictors. Clinical parameters, including blood pressure, complete blood count, and coagulation function, were also considered. The predictive value was evaluated through receiver operating characteristic curve analysis.
The poor prognosis group exhibited lower FIB but higher FDP, D-D, FDP/FIB ratio, and white blood cell count (WBC) (all P<0.01). Additionally, this group had longer prothrombin time and activated partial thromboplastin time (both P<0.01) as well as greater plasma transfusion volumes (P<0.05). An inverse relationship was identified between FIB and FDP/D-D levels across prognosis groups. However, positive FDP/D-D correlation was observed only in the poor prognosis group, with no significant FDP/D-D linkage found in the good prognosis group; moreover, these correlations were stronger in cases with worse clinical outcomes. Multivariate analysis identified FIB, FDP, D-D, and WBC as independent predictors. The combined biomarker model (area under the curve (AUC) =0.923) outperformed individual markers (AUC range: 0.691-0.809).
FIB, FDP, D-D, and WBC are significant predictors of transfusion outcomes in trauma patients. A combined biomarker model demonstrates superior predictive performance, highlighting the importance of identifying coagulation dysregulation in trauma prognosis.
探讨凝血生物标志物(纤维蛋白原[FIB]、纤维蛋白降解产物[FDP]、D-二聚体[D-D]、FDP/FIB比值)在预测创伤患者输血结局中的作用。
对112例创伤病例(2020年5月至2024年5月)进行回顾性分析,根据输血结局将其分为预后良好组(n = 80)和预后不良组(n = 32)。比较两组输血前凝血生物标志物水平。采用Pearson相关性分析评估标志物之间的关联,并通过逻辑回归确定结局预测因子。还考虑了包括血压、全血细胞计数和凝血功能在内的临床参数。通过受试者工作特征曲线分析评估预测价值。
预后不良组的FIB水平较低,但FDP、D-D、FDP/FIB比值和白细胞计数(WBC)较高(均P<0.01)。此外,该组的凝血酶原时间和活化部分凝血活酶时间较长(均P<0.01),血浆输注量也较大(P<0.05)。在不同预后组中,FIB与FDP/D-D水平呈负相关。然而,仅在预后不良组中观察到FDP/D-D呈正相关,在预后良好组中未发现显著的FDP/D-D关联;此外,在临床结局较差的病例中,这些相关性更强。多因素分析确定FIB、FDP、D-D和WBC为独立预测因子。联合生物标志物模型(曲线下面积[AUC]=0.923)优于单个标志物(AUC范围:0.691-0.809)。
FIB、FDP、D-D和WBC是创伤患者输血结局的重要预测因子。联合生物标志物模型具有卓越的预测性能,凸显了识别创伤预后中凝血功能失调的重要性。