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中国临床研究英文版:2026,39(5):692-696
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HA380血液灌流联合血必净治疗脓毒症患者的疗效及对血清IL-17和Presepsin水平的影响
(1. 沧州市中心医院急诊医学部, 河北 沧州 061000;2. 沧州市中心医院呼吸与危重症医学二科, 河北 沧州 061000)
The efficacy of HA380 hemoperfusion combined with Xuebijing on sepsis patients and its impacts on serum IL-17 and Presepsin levels
摘要
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Received:July 25, 2025   Published Online:May 22, 2026
中文摘要: 目的 观察HA380血液灌流联合血必净注射液用于脓毒症患者的临床价值,分析其对患者血清白细胞介素(IL)-17、可溶性白细胞分化抗原14亚型(Presepsin)水平的作用。方法 前瞻性选取沧州市中心医院2021年12月至2023年6月收治的120例脓毒症患者为研究对象,采用随机数字表法分为血必净组和联合组,各60例。研究过程中共脱落15例,最终血必净组纳入52例,联合组53例。血必净组给予血必净注射液治疗,联合组给予血必净注射液联合HA-380树脂血液灌流器治疗。两组疗程均为1周。观察两组患者治疗前和治疗1周的血液指标、相关评分以及治疗1周的临床疗效和不良反应情况。结果 治疗1周后,联合组患者总有效率显著高于血必净组(94.34% vs 80.77%,χ2=4.456,P=0.035);两组患者血清IL-17、肿瘤坏死因子-α(TNF-α)、降钙素原(PCT)、Presepsin、血清肌酐、血尿素氮、动脉血二氧化碳分压(PaCO2)水平和急性生理学与慢性健康状况评分系统Ⅱ(APACHE-Ⅱ)评分、序贯器官衰竭评估(SOFA)评分显著降低(P<0.05),且联合组显著低于血必净组(P<0.05);两组患者动脉血氧饱和度(SaO2)、酸碱度(pH 值)显著升高(P<0.05),且联合组显著高于血必净组(P<0.05)。联合组患者不良反应总发生率显著低于血必净组(5.66% vs 19.23%,χ2=4.456,P=0.035)。结论 HA380血液灌流联合血必净治疗脓毒症患者的疗效显著,可改善患者预后,降低患者血清IL-17和Presepsin水平。
Abstract:Objective To observe the clinical value of the HA380 hemoperfusion combined with Xuebijing injection for patients with sepsis,and analyze the effect of this regimen on the serum levels of interleukin(IL-17 and soluble leukocyte differentiation antigen 14 subtype(Presepsin)in patients. Methods A total of 120 sepsis patients admitted to Cangzhou Central Hospital between December 2021 and June 2023 were enrolled prospectively,and randomly divided into two groups:the Xuebijing group(n=60)and the combined group(n=60)using a random number table.During the study,15 cases were excluded due to dropout,resulting in 52 cases in the Xuebijing group and 53 cases in the combined group. The Xuebijing group received intravenous Xuebijing injection,while the combined group received Xuebijing injection combined with HA380 hemoperfusion therapy. The treatment course for both groups lasted one week.The blood indicators and relevant scores of the two groups of patients before treatment and after one week of treatment,as well as the clinical efficacy and adverse reactions after one week of treatment were observed. Results After one week of treatment,the total effective rate was significantly higher in the combined group than that in the Xuebijing group (94.34% vs 80.77%,χ2=4.456,P=0.035). Serum levels of IL- 17,tumor necrosis factor- α(TNF- α), procalcitonin(PCT),Presepsin,serum creatinine,blood urea nitrogen,and arterial partial pressure of carbon dioxide(PaCO2),as well as Acute Physiology and Chronic Health Evaluation Ⅱ(APACHE - Ⅱ)score and Sequential Organ Failure Assessment(SOFA)score,were significantly reduced in both groups(P<0.05),with the combined group showing significantly lower levels than the Xuebijing group(P<0.05). Conversely,arterial oxygen saturation(SaO2)levels and pondus hydrogenii(pH)values were significantly increased in both groups(P<0.05),with significantly higher levels in the combined group than in the Xuebijing group(P<0.05). The incidence of adverse reactions was significantly lower in the combined group than in the Xuebijing group(5.66% vs 19.23%,χ2=4.456,P=0.035). Conclusion The combination of HA380 hemoperfusion and Xuebijing has significant therapeutic effects on sepsis patients,which can improve the prognosis of patients and reduce the levels of serum IL-17 and Presepsin.
文章编号:     中图分类号:R631 R459.5    文献标志码:A
基金项目:沧州市重点研发计划指导项目(213106053)
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