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外周血白细胞水平对脑挫裂伤血肿进展的预测作用

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目的 探究外周血白细胞水平对脑挫裂伤患者颅内血肿进展的预测作用.方法 回顾性分析2021年1月至2023年1月扬州大学附属医院神经外科收治的248例脑挫裂伤患者的临床资料.根据受伤后24 h内的头颅CT结果确定血肿是否进展(血肿体积增大>25%或新发颅内血肿).比较非进展组与进展组患者的性别、年龄、入院时的格拉斯哥昏迷评分(GCS)、血肿类型(硬膜下血肿和硬膜外血肿)、血肿位置、既往病史、是否手术,以及发病后24 h内的外周血实验室相关指标[包括白细胞、中性粒细胞、淋巴细胞、单核细胞、血小板计数,肌酐、D-二聚体水平,凝血酶原时间(PT)、活化部分凝血活酶时间(APTT),中性粒细胞与淋巴细胞比值(NLR)、系统性免疫炎症指数(SII)、单核细胞与淋巴细胞比值(MLR)、血小板与淋巴细胞比值(PLR)、衍生NLR(dNLR)]的差异.将上述指标中P<0.1的指标纳入到多因素logistic回归模型中,分析外周血白细胞水平对患者血肿进展的影响.绘制受试者工作特征曲线(ROC)并计算曲线下面积(AUC),评估白细胞水平对脑挫裂伤患者血肿进展的预测作用.结果 248例患者中,非进展组142例,进展组106例.非进展组外周血白细胞计数[M(Q1,Q3)]为 12.53(9.19,15.45)×109/L,进展组为 13.01(10.83,15.76)× 109/L,差异有统计学意义(P=0.043).多因素logistic回归分析显示,除入院时GCS低(OR=0.84,95%CI:0.73~0.96)、有抗凝或抗血小板药物使用史(OR=1.34,95%CI:1.12~1.97)外,外周血白细胞计数升高(OR=1.16,95%CI:1.01~1.32)、MLR 升高(OR=3.55,95%CI:1.19~10.60)均是脑挫裂伤血肿进展的独立影响因素(均P<0.05).根据入院时GCS+抗凝或抗血小板药物使用史构建的ROC曲线预测脑挫裂伤血肿进展的AUC为0.60;根据入院时GCS+抗凝或抗血小板药物使用史+周血白细胞计数+MLR构建的ROC曲线预测脑挫裂伤血肿进展的AUC为0.75.结论 外周血白细胞水平是脑挫裂伤患者血肿进展的重要影响因素,对患者血肿进展有预测价值.
The predictive effect of peripheral blood leukocyte levels on the progression of hematoma after cerebral contusion and laceration
Objective To explore the predictive value of peripheral blood leukocyte levels for hematoma progression in patients with cerebral contusion and laceration.Methods A retrospective analysis was conducted on clinical data of 248 patients with cerebral contusion and laceration who were admitted to the Department of Neurosurgery at Affiliated Hospital of Yangzhou University from January 2021 to January 2023.Hematoma progression was determined based on CT scan results within 24 hours after injury(hematoma volume increased by more than 25%or new intracranial hematoma).Gender,age,Glasgow Coma Scale(GCS)at admission,hematoma type(subdural hematoma or epidural hematoma),hematoma location,medical history,surgical intervention,and peripheral blood laboratory parameters within 24 hours post-onset[including white blood cells,neutrophils,lymphocytes,monocytes,platelets,creatinine,D-dimer levels,prothrombin time(PT),activated partial thromboplastin time(APTT),neutrophil-to-lymphocyte ratio(NLR),systemic immune-inflammatory index(SII),monocyte-to-lymphocyte ratio(MLR),platelet-to-lymphocyte ratio(PLR),derived NLR(dNLR)]were compared between the non-progression group and progression group.Factors with a significance level of P<0.1 were included in a multivariate logistic regression model to analyze the impact of leukocyte levels on hematoma progression.Receiver operating characteristic(ROC)curves were generated,and the area under the curve(AUC)was calculated to assess the predictive value of leukocyte levels for hematoma progression in cerebral contusion patients.Results Among the 248 patients,142 were in the non-progression group and 106 in the progression group.The white blood cell count[M(Q1,Q3)]was 12.53(9.19,15.45)x 109/L in the non-progression group and 13.01(10.83,15.76)x 109/L in the progression group,with a statistically significant difference(P=0.043).Multivariate logistic regression analysis showed that,in addition to low GCS at admission(OR=0.84,95%CI:0.73-0.96)and a history of anticoagulant or antiplatelet use(OR=1.34,95%CI:1.12-1.97),an increase in white blood cell count(0R=1.16,95%CI:1.01-1.32)and a decrease in MLR(OR=3.55,95%CI:1.19-10.60)were independent factors influencing hematoma progression in cerebral contusion(all P<0.05).The ROC curve model constructed based on these parameters showed an AUC of 0.60 for predicting hematoma progression with GCS at admission and a history of anticoagulant or antiplatelet use.When white blood cell count and MLR were added to the model,the AUC increased to 0.75.Conclusion The level of peripheral blood leukocytes is an important factor influencing the progression of hematoma in patients with cerebral contusion and laceration,and has predictive value for the progression of hematoma in patients.

Brain injuries,traumaticLeukocytesHematomaForecastingProgression

张华军、段晓春、庄国权、张一妙、李运帷、邵利英、齐文涛

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扬州大学附属医院神经外科,扬州 225001

大连医科大学研究生院,大连 116000

陕西中医药大学研究生院,咸阳 712046

脑损伤,创伤性 白细胞 血肿 预测 进展

2024

中华神经外科杂志
中华医学会

中华神经外科杂志

CSTPCD北大核心
影响因子:1.107
ISSN:1001-2346
年,卷(期):2024.40(5)
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