Effect of an Herbal-Based Injection on 28-Day Mortality in Patients With Sepsis The EXIT-SEP Randomized Clinical Trial

作者：Liu, Songqiao; Yao, Chen; Xie, Jianfeng; Liu, Hong; Wang, Hongliang; Lin, Zhaofen; Qin, Bingyu; Wang, Difen; Lu, Weihua; Ma, Xiaochun; Liu, Yan; Liu, Ling; Zhang, Chi; Xu, Lei; Zheng, Ruiqiang; Zhou, Feihu; Liu, Zhongmin; Zhang, Guoqiang; Zhou, Lixin; Liu, Jian; Fei, Aihua; Zhang, Guoxiu; Zhu, Yimin; Qian, Kejian; Wang, Ruilan; Liang, Yafeng; Duan, Meili; Wu, Dawei; Sun, Rongqing; Wang, Ying; Zhang, Xijing; Cao, Quan; Yang, Mingshi; Jin, Minggen; Song, Yan; Huang, Ling; Zhou, Fachun

来源：JAMA Internal Medicine, 2023, 183(7): 647-655.

DOI：10.1001/jamainternmed.2023.0780

• XUEBIJING INJECTION
• INJURY

Importance Previous research has suggested that Xuebijing injection (XBJ), an herbal-based intravenous preparation, may reduce mortality among patients with sepsis.Objective To determine the effect of XBJ vs placebo on 28-day mortality among patients with sepsis.Design, Setting, and Participants The Efficacy of Xuebijing Injection in Patients With Sepsis (EXIT-SEP) trial was a multicenter, randomized double-blind, placebo-controlled trial conducted in intensive care units at 45 sites and included 1817 randomized patients with sepsis (sepsis 3.0) present for less than 48 hours. Patients aged 18 to 75 years with a Sequential Organ Failure Assessment score of 2 to 13 were enrolled. The study was conducted from October 2017 to June 2019. The final date of follow-up was July 26, 2019. Data analysis was performed from January 2020 to August 2022.Interventions The patients were randomized to receive either intravenous infusion of XBJ (100 mL, n = 911) or volume-matched saline placebo (n = 906) every 12 hours for 5 days.Main Outcomes and Measures The primary outcome was 28-day mortality.Results Among the 1817 patients who were randomized (mean [SD] age, 56.5 [13.5] years; 1199 [66.0%] men), 1760 (96.9%) completed the trial. In these patients, the 28-day mortality rate was significantly different between the placebo group and the XBJ group (230 of 882 patients [26.1%] vs 165 of 878 patients [18.8%], respectively; P < .001). The absolute risk difference was 7.3 (95% CI, 3.4-11.2) percentage points. The incidence of adverse events was 222 of 878 patients (25.3%) in the placebo group and 200 of 872 patients (22.9%) in the XBJ group.Conclusions and Relevance In this randomized clinical trial among patients with sepsis, the administration of XBJ reduced 28-day mortality compared with placebo.

• 单位
  吉林大学; 青岛大学; 复旦大学; 兰州大学; 武汉大学; 北京大学; 中国医科大学; 南昌大学; 上海交通大学; 1; 哈尔滨医科大学; 郑州大学; 中国科学院; 佛山市第一人民医院; 内蒙古医学院