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乌司他丁联合胸腺法新治疗脓毒症患者的临床研究

赵璟 冯丽霞 史晶心 范风江

中国临床药理学杂志2025,Vol.41Issue(4):467-471,5.
中国临床药理学杂志2025,Vol.41Issue(4):467-471,5.DOI:10.13699/j.cnki.1001-6821.2025.04.004

乌司他丁联合胸腺法新治疗脓毒症患者的临床研究

Clinical trial of ulinastatin combined with thymalfasin α1 in the treatment of patients with sepsis

赵璟 1冯丽霞 1史晶心 1范风江1

作者信息

  • 1. 南阳市第一人民医院综合重症监护室,河南南阳 473000||南阳市第一人民医院脓毒症转化医学重点实验室,河南南阳 473000
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摘要

Abstract

Objective To observe the clinical efficacy of ulinastatin injection and thymalfasin for injection in the treatment of sepsis patients and their effects on peripheral blood T lymphocyte subsets.Methods Sepsis patients were divided into control group and treatment group according to the cohort method.The control group was treated with ulinastatin injection in addition to initial resuscitation,hemoperfusion,and antimicrobial therapy.The treatment regimen was intravenous infusion,2.0 × 105 U bid for 4 days,followed by intravenous pump infusion,1.0 × 105 U bid for 6 days.The treatment group received thymalfasin for injection on base of the control group's treatment,subcutaneous injection,1.6 mg twice a week,for 2 weeks.The clinical efficacy,Sequential Organ Failure Assessment(SOFA)score,Acute Physiology and Chronic Health Evaluation(APACHE)Ⅱ score,peripheral blood procalcitonin(PCT),lactate(Lac),D-dimer(D-D),and levels of T lymphocyte subsets were compared between the two groups,as well as 28-day mortality rate and safety were evaluated.Results A total of 43 patients were enrolled in the control group and 37 patients in the treatment group.After treatment,the total effective rates in the treatment group and the control group were 94.59%(35 cases/37 cases)and 86.05%(37 cases/43 cases),respectively,with no significant difference statistically(P>0.05).After treatment,the SOFA scores in the treatment group and the control group were(5.46±1.20)and(6.71±1.33)points;the APACHE Ⅱ scores were(16.17±3.49)and(18.63±3.82)points;the peripheral blood PCT levels were(1.51±0.33)and(1.88±0.42)μg·L-1;the Lac levels were(2.73±0.52)and(5.06±1.19)nmol·L-1;the D-D levels were(0.85±0.27)and(1.02±0.33)mg·L-1;the CD3+levels were(38.98±4.36)%and(34.42±4.14)%;the CD4+levels were(18.66±2.47)%and(13.17±1.96)%;the CD8+levels were(12.35±1.42)%and(13.01±1.39)%;and the CD4+/CD8+ratio were 1.49±0.24 and 1.04±0.22,respectively,all showing statistically significant differences(all P<0.05).The 28-day mortality rates in the treatment group and the control group were 18.92%(7 cases/37 cases)and 23.26%(10 cases/43 cases),respectively,with no significant difference statistically(P>0.05).No drug-related adverse reactions were observed in either group.Conclusion The clinical efficacy of thymalfasin for injection in the treatment of sepsis is more ideal than that of ulinastatin alone,as it can better reduce the levels of peripheral PCT,Lac,and D-D,regulate T lymphocyte subsets,demonstrating definite efficacy and safety.

关键词

注射用胸腺法新/乌司他丁注射液/脓毒症/降钙素原/乳酸/D-二聚体/T淋巴细胞亚群

Key words

thymalfasin for injection/ulinastatin injection/sepsis/procalcitonin/lactic acid/D-dimer/T lymphocyte subsets

分类

药学

引用本文复制引用

赵璟,冯丽霞,史晶心,范风江..乌司他丁联合胸腺法新治疗脓毒症患者的临床研究[J].中国临床药理学杂志,2025,41(4):467-471,5.

中国临床药理学杂志

OA北大核心

1001-6821

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