胸腺肽α1联合乌司他丁辅助治疗多重耐药菌感染重症肺炎的疗效

Efficacy of thymosin α1 combined with ulinastatin in treating severe pneumonia caused by multidrug-resistant bacteria

  • 摘要:
    目的 探讨胸腺肽α1联合乌司他丁在多药耐药菌感染重症肺炎患者中的辅助治疗效果。
    方法 回顾性收集2022年1月-2024年1月于西安交通大学附属红会医院治疗的多药耐药菌感染重症肺炎患者的临床资料,经1∶1倾向性评分匹配后,对照组、研究组各纳入75例,对照组依据药敏结果采用常规治疗,研究组在对照组基础上采用胸腺肽α1联合乌司他丁治疗。比较两组临床疗效,临床症状改善时间及相关指标(体温恢复正常时间、肺部啰音消失时间、重症监护室停留时间、住院时间、呼吸机撤机时间),病情程度,病原菌清除情况、28 d病死率、用药不良反应率;检测并比较两组患者治疗前、治疗后T淋巴细胞亚群(CD8+、CD4+、CD3+及CD4+/CD8+)、炎症因子水平C-反应蛋白(CRP)、降钙素原(PCT)、肿瘤坏死因子-α(TNF-α)、白细胞介素-10(IL-10)。
    结果 研究组疗效优于对照组(P=0.020);研究组体温恢复正常时间、肺部啰音消失时间、重症监护室停留时间、呼吸机撤机时间分别为(3.52±0.78)、(13.62±2.40)、(7.22±1.05)、(3.54±1.22)d,均短于对照组(P<0.05);研究组病原菌清除率为90.67%,高于对照组(P<0.001);治疗14 d时,研究组CD4+、CD3+、CD4+/CD8+、IL-10分别为(47.55±2.11)、(49.55±2.17)、(1.73±0.28)、(133.51±14.71)pg/L,高于对照组,CD8+、CRP、PCT、TNF-α分别为(27.44±1.85)、(19.05±3.51)mg/L、(0.61±0.24)μg/L、(55.02±7.51)ng/L,低于对照组(P<0.05);两组28 d病死率、用药不良反应差异无统计学意义。
    结论 胸腺肽α1联合乌司他丁在多药耐药菌感染重症肺炎患者中具有良好的辅助治疗效果,有助于提高病原菌清除率及免疫功能状态,降低炎症因子水平,缓解病情进展。

     

    Abstract:
    OBJECTIVE  To investigate the adjuvant therapeutic effect of thymosin α1 combined with ulinastatin in patients with severe pneumonia caused by multidrug-resistant bacteria.
    METHODS  A retrospective collection of clinical data was conducted on patients with severe pneumonia caused by multidrug-resistant bacteria, who were treated at Honghui Hospital Affiliated to Xi'an Jiaotong University from Jan. 2022 to Jan. 2024. After 1∶1 propensity score matching, the patients were assigned as the control group and the study group with is cases in each group. The control group received conventional treatment based on drug susceptibility results, while the study group received thymosin α1 combined with ulinastatin in addition to the treatment given to the control group. Clinical efficacy, time of clinical symptom improvement, relevant indicators (time required for body temperature normalization, disappearance time of pulmonary rales, length of stay in the intensive care unit, hospital stay and ventilator weaning time), disease severity, pathogen clearance, 28-day mortality rate and the rate of adverse drug reactions were compared between the two groups. T lymphocyte subsets (CD8+, CD4+, CD3+ and CD4+/CD8+) and levels of inflammatory factors C-reactive protein (CRP), procalcitonin (PCT), tumor necrosis factor-α (TNF-α) and interleukin-10 (IL-10) were measured and compared between the two groups before and after treatment.
    RESULTS  The therapeutic efficacy in the study group was superior to that in the control group (P=0.020). The time required for body temperature normalization, disappearance time of pulmonary rales, length of stay in the intensive care unit and ventilator weaning time in the study group were (3.52±0.78) days, (13.62±2.40) days, (7.22±1.05) days and (3.54±1.22) days, respectively, all shorter than those in the control group (P<0.05). The clearance rate of pathogens in the study group was 90.67%, higher than that in the control group (P<0.001). On day 14 of treatment, the levels of CD4+, CD3+, CD4+/CD8+ and IL-10 in the study group were (47.55±2.11), (49.55±2.17), (1.73±0.28) and (133.51±14.71) pg/L, respectively, higher than those in the control group, while the levels of CD8+, CRP, PCT and TNF-α were (27.44±1.85), (19.05±3.51) mg/L, (0.61±0.24) μg/L and (55.02±7.51) ng/L, respectively, lower than those in the control group (P<0.05). There was no statistically significant difference in the 28-day mortality rate or adverse drug reactions between the two groups.
    CONCLUSIONS  Thymosin α1 combined with ulinastatin demonstrates favorable effects in patients with severe pneumonia caused by multidrug-resistant bacteria, which contributes to improving pathogen clearance rates and immune function status, reducing levels of inflammatory factors, and alleviating disease progression.

     

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