Xiang Yanping, Li Renhua, Cai Jia, Jiang Qian
Department of Infectious Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing, People's Republic of China.
Ther Clin Risk Manag. 2024 Oct 25;20:731-740. doi: 10.2147/TCRM.S485620. eCollection 2024.
This study aimed to investigate clinical efficacy, safety and short-term prognosis of plasma exchange (PE), plasma perfusion combining PE (PP+PE), dual-plasma molecular adsorption system combining PE (DPMAS+PE) in treating acute-on-chronic liver failure (ACLF).
Two hundred and fourteen ACLF patients admitted to our hospital were included and divided into PE (n = 72), PP+PE (n = 75), DPMAS+PE group (n = 67). Laboratory indexes and MELD scores were collected, and clinical efficacy was compared. Patients' adverse reactions during and 24-h after treatment were collected, and safety was compared. Survival status of patients was followed-up within 90 days, and prognosis was analyzed.
PE, PP+PE and DPMAS+PE significantly reduce TBiL, DBiL, ALT, AST, SA, PT, INR, PCT and CRP levels, and increase PA and PTA levels, compared with pre-treatments ( < 0.05). WBC and SCR levels in DPMAS+PE group decreased significantly post-treatment ( < 0.05). Na and Cl levels in PE and PP+PE group decreased significantly post-treatment ( < 0.05). Total adverse reaction incidence in PE, PP+PE, DPMAS+PE group were 38.89%, 22.70%, 17.90%, respectively, with significant differences among three groups ( < 0.05). Ninety-day mortality rates of patients in PE, PP+PE, DPMAS+PE group were 41.67%, 34.67%, 20.90%, respectively, with significant differences among three groups ( < 0.05).
PE, PP+PE and DPMAS+PE three artificial liver treatment modes can effectively improve liver, kidney and coagulation function of ACLF patients. DPMAS+PE demonstrated better ability to remove endotoxin and inflammatory mediators, showed advantages in reducing ACLF patient mortality within 90 days, and had the least impact on electrolyte post-treatment. Therefore, DPMAS+PE can be used as a better choice for clinical treatment.
本研究旨在探讨血浆置换(PE)、血浆灌流联合血浆置换(PP + PE)、双重血浆分子吸附系统联合血浆置换(DPMAS + PE)治疗慢加急性肝衰竭(ACLF)的临床疗效、安全性及短期预后。
纳入我院收治的214例ACLF患者,分为PE组(n = 72)、PP + PE组(n = 75)、DPMAS + PE组(n = 67)。收集实验室指标及终末期肝病模型(MELD)评分,比较临床疗效。收集患者治疗期间及治疗后24小时的不良反应,比较安全性。随访患者90天内的生存状况,分析预后。
与治疗前比较,PE、PP + PE及DPMAS + PE均能显著降低总胆红素(TBiL)、直接胆红素(DBiL)、谷丙转氨酶(ALT)、谷草转氨酶(AST)、血清淀粉样蛋白A(SA)、凝血酶原时间(PT)、国际标准化比值(INR)、降钙素原(PCT)及C反应蛋白(CRP)水平,提高前白蛋白(PA)及凝血酶原活动度(PTA)水平(P < 0.05)。DPMAS + PE组治疗后白细胞(WBC)及血肌酐(SCR)水平显著降低(P < 0.05)。PE组及PP + PE组治疗后血钠(Na)及血氯(Cl)水平显著降低(P < 0.05)。PE组、PP + PE组、DPMAS + PE组总不良反应发生率分别为38.89%、22.70%、17.90%,三组比较差异有统计学意义(P < 0.05)。PE组、PP + PE组、DPMAS + PE组患者90天死亡率分别为41.67%、34.67%、20.90%,三组比较差异有统计学意义(P < 0.05)。
PE、PP + PE及DPMAS + PE三种人工肝治疗模式均可有效改善ACLF患者的肝脏、肾脏及凝血功能。DPMAS + PE清除内毒素及炎症介质能力更强,在降低ACLF患者90天死亡率方面具有优势,且治疗后对电解质影响最小。因此,DPMAS + PE可作为临床治疗的较好选择。