Gong Zhao-Tang, Yang Hong-Xin, Zhu Ben-Ben, Liu Huan-Huan, Siri Guleng
Department of Pharmacy, Inner Mongolia Autonomous Region People's Hospital, Hohhot 010017, Inner Mongolia Autonomous Region, China; Department of Pharmacy, Inner Mongolia Medical University, Hohhot 010110, Inner Mongolia Autonomous Region, China.
Department of Pharmacy, Inner Mongolia Autonomous Region People's Hospital, Hohhot 010017, Inner Mongolia Autonomous Region, China.
J Integr Med. 2024 Nov;22(6):645-651. doi: 10.1016/j.joim.2024.08.006. Epub 2024 Aug 30.
The objective of this study was to investigate the clinical efficacy and safety of treating sepsis patients with Xuebijing injection (XBJI).
We conducted a retrospective analysis of 418 patients who experienced severe infections and were treated with XBJI from June 2018 to June 2021. Propensity score matching was used to match the patient cases. The study population included 209 pairs of cases (418 individuals), and the analysis included data from before and after a 14-day course of treatment with carbapenem alone, or carbapenem with XBJI.
There were no significant differences in the 14-day mortality or length of hospital stay (P > 0.05) between the two groups. The combined treatment group had more patients with C-reactive protein that returned to normal levels (compared to baseline) than the non-combined treatment group (14.4% vs 8.1%; odds ratio [OR]: 0.528; 95% confidence interval [CI]: 0.282-0.991; P = 0.026). Similarly, the combined treatment group had higher procalcitonin attainment rate (55.0% vs 39.7%; OR: 0.513; 95% CI: 0.346-0.759; P = 0.001) than the non-combined treatment group. Further, more patients in the combined treatment group achieved normal creatinine levels than in the non-combined treatment group (64.1% vs 54.1%; OR: 0.659; 95% CI: 0.445-0.975; P = 0.037).
The combination of XBJI with carbapenem did not reduce the 14-day mortality rate of patients with severe infection, but it was able to reduce the level of inflammatory factors in patients with sepsis, and had a protective effect on liver and kidney function. Please cite this article as: Gong ZT, Yang HX, Zhu BB, Liu HH, Siri GL. Clinical efficacy of Xuebijing injection for the treatment of sepsis: A retrospective cohort study. J Integr Med. 2024; 22(6): 645-651.
本研究旨在探讨血必净注射液(XBJI)治疗脓毒症患者的临床疗效及安全性。
我们对2018年6月至2021年6月期间418例经历严重感染并接受血必净治疗的患者进行了回顾性分析。采用倾向得分匹配法对患者病例进行匹配。研究人群包括209对病例(418例个体),分析包括单独使用碳青霉烯类药物或碳青霉烯类药物联合血必净治疗14天疗程前后的数据。
两组患者的14天死亡率和住院时间无显著差异(P>0.05)。联合治疗组中C反应蛋白恢复至正常水平(相对于基线)的患者比非联合治疗组更多(14.4%对8.1%;优势比[OR]:0.528;95%置信区间[CI]:0.282-0.991;P=0.026)。同样,联合治疗组的降钙素原达标率高于非联合治疗组(55.0%对39.7%;OR:0.513;95%CI:0.346-0.759;P=0.001)。此外,联合治疗组中肌酐水平恢复正常的患者比非联合治疗组更多(64.1%对54.1%;OR:0.659;95%CI:0.445-0.975;P=0.037)。
血必净联合碳青霉烯类药物并未降低严重感染患者的14天死亡率,但能够降低脓毒症患者的炎症因子水平,并对肝肾功能有保护作用。请引用本文:龚ZT,杨HX,朱BB,刘HH,西里GL。血必净注射液治疗脓毒症的临床疗效:一项回顾性队列研究。《整合医学杂志》。2024;22(6):645-651。