Li Chuanlei, Xie Yun, Zheng Zhihuang, Xu Kexin, Zhu Nan, Zang Xiujuan, Wang Xuemin, Bao Jinfang, Yu Qing, Wang Ruilan, Liu Jun, Zhou Zhigang
Department of Nephrology, Shanghai General Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 201620, China.
Department of Intensive Care Unit, Shanghai General Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 201620, China.
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2021 Jul;33(7):815-820. doi: 10.3760/cma.j.cn121430-20201228-00776.
To investigate the clinical effect of Jiedu Limai decoction in septic patients with syndrome of heat-toxin exuberance.
A prospective randomized controlled trial was conducted. From March 2019 to April 2020, septic patients with syndrome of heat-toxin exuberance admitted to intensive care unit (ICU) of Shanghai General Hospital and Songjiang Branch of Shanghai General Hospital were enrolled as the research objects, and they were divided into routine treatment group and Jiedu Limai decoction group by the random number table method. Patients in both groups were given standard treatment in accordance with the guidelines, and patients in the Jiedu Limai decoction group were given Jiedu Limai decoction in addition to the standard treatment, once a day for 14 days. The 28-day survival of patients of the two groups were recorded, the acute physiology and chronic health evaluation II (APACHE II) score, sequential organ failure assessment (SOFA) score, coagulation indexes, infection indexes, inflammatory cytokines and organ function indicators before treatment and 7 days after treatment in both groups were recorded, and the prognosis of the two groups were recorded.
A total of 259 patients with infection or clinical diagnosis of infection admitted during the experimental observation period were included, and those who did not meet the Sepsis-3 diagnostic criteria, more than 80 years old or less than 18 years old, with multiple tumor metastases, autoimmune system diseases, with length of ICU stay less than 24 hours, with acute active gastrointestinal bleeding and with incomplete data were excluded. One hundred patients were finally enrolled, with 50 patients in the routine treatment group and 50 patients in the Jiedu Limai decoction group. There were no statistically significant differences in coagulation indexes, infection indicators, inflammatory cytokines and organ function indicators before treatment between the two groups. After 7 days of treatment, the coagulation indexes, infection biomarkers and inflammatory cytokines in the Jiedu Limai decoction group were significantly lower than those in the routine treatment group [D-dimer (mg/L): 2.2 (1.8, 8.5) vs. 4.0 (1.5, 8.7), fibrinogen (Fib, g/L): 3.7 (3.4, 4.3) vs. 4.2 (3.7, 4.3), fibrinogen degradation product (FDP, mg/L): 7.2 (5.4, 10.2) vs. 13.2 (9.2, 15.2), procalcitonin (PCT, μg/L): 0.4 (0.2, 2.9) vs. 0.5 (0.2, 0.9), C-reactive protein (CRP, mg/L): 50.1 (9.5, 116.0) vs. 75.1 (23.5, 115.2), interleukin-6 (IL-6, ng/L): 31.6 (21.6, 81.0) vs. 44.1 (14.0, 71.3), all P < 0.05], and the levels of B-type brain natriuretic peptide (BNP) and kidney injury molecule-1 (KIM-1) were significantly lowered [BNP (ng/L): 261.1 (87.5, 360.3) vs. 347.3 (128.8, 439.4), KIM-1 (μg/L): 0.86 (0.01, 1.40) vs. 1.24 (1.05, 1.57), both P < 0.05]. Compared with the routine treatment group, the number of new organ failure in the Jiedu Limai decoction group was decreased (30.0% vs. 50.0%, P < 0.05). Although there was no significant difference in 28-day mortality between the two groups (P > 0.05), the 28-day mortality in the Jiedu Limai decoction group was lower than that in the routine treatment group (18.0% vs. 24.0%).
Combining Jiedu Limai decoction to the sepsis guideline in treating syndrome of heat-toxin exuberance can effectively improve patients' coagulation function, the situation of heart and renal injury, reduce the level of inflammatory cytokines, and fewer people develop new organ failure after treatment.
探讨解毒利脉汤对热毒炽盛型脓毒症患者的临床疗效。
进行一项前瞻性随机对照试验。选取2019年3月至2020年4月在上海交通大学医学院附属瑞金医院重症医学科及上海交通大学医学院附属瑞金医院松江分院收治的热毒炽盛型脓毒症患者作为研究对象,采用随机数字表法将其分为常规治疗组和解毒利脉汤组。两组患者均按照指南给予标准治疗,解毒利脉汤组患者在标准治疗基础上加用解毒利脉汤,每日1剂,连续服用14天。记录两组患者28天生存率,记录两组患者治疗前及治疗7天后的急性生理与慢性健康状况评分系统Ⅱ(APACHEⅡ)评分、序贯器官衰竭评估(SOFA)评分、凝血指标、感染指标、炎症因子及器官功能指标,并比较两组患者预后。
实验观察期间共纳入259例感染或临床诊断为感染的患者,排除不符合脓毒症-3诊断标准、年龄大于80岁或小于18岁、有多发肿瘤转移、自身免疫系统疾病、入住重症监护病房时间小于24小时、急性活动性消化道出血及资料不全者。最终纳入100例患者,常规治疗组50例,解毒利脉汤组50例。两组患者治疗前凝血指标、感染指标、炎症因子及器官功能指标比较,差异均无统计学意义。治疗7天后,解毒利脉汤组患者凝血指标、感染生物标志物及炎症因子水平均显著低于常规治疗组[D-二聚体(mg/L):2.2(1.8,8.5)比4.0(1.5,8.7),纤维蛋白原(Fib,g/L):3.7(3.4,4.3)比4.2(3.7,4.3),纤维蛋白原降解产物(FDP,mg/L):7.2(5.4,10.2)比13.2(9.2,15.2),降钙素原(PCT,μg/L):0.4(0.2,2.9)比0.5(0.2,0.9),C反应蛋白(CRP,mg/L):50.1(9.5,116.0)比75.1(23.5,115.2),白细胞介素-6(IL-6,ng/L):31.6(21.6,81.0)比44.1(14.0,71.3),均P<0.05],B型脑钠肽(BNP)及肾损伤分子-1(KIM-1)水平也显著降低[BNP(ng/L):261.1(87.5,360.3)比347.3(128.8,439.4),KIM-1(μg/L):0.86(0.01,1.40)比1.24(1.05,1.57),均P<0.05]。与常规治疗组比较,解毒利脉汤组患者新发生器官衰竭例数减少(30.0%比50.0%,P<0.05)。两组患者28天死亡率比较,差异无统计学意义(P>0.05),但解毒利脉汤组28天死亡率低于常规治疗组(18.0%比24.0%)。
在脓毒症指南基础上联用解毒利脉汤治疗热毒炽盛型脓毒症,可有效改善患者凝血功能、心肾损伤情况,降低炎症因子水平,治疗后新发生器官衰竭者较少。