肝脏 ›› 2025, Vol. 30 ›› Issue (1): 24-30.

• 肝功能衰竭 • 上一篇    下一篇

双重血浆分子吸附系统在HBV相关慢加急性肝衰竭患者中的疗效分析

张冬青, 廖资渊, 林升龙, 吴雯军, 王香梅, 马华皙, 高海兵   

  1. 350028 福州 福建医科大学孟超肝胆医院重症肝病科
  • 收稿日期:2023-11-30 出版日期:2025-01-31 发布日期:2025-03-10
  • 通讯作者: 高海兵,Email:gaohb605@163.com
  • 基金资助:
    北京肝胆相照公益基金会人工肝专项基金(iGandanF-1082022-RGG047);福州市科技计划项目(2022-S-012);福建省自然科学基金资助项目(2022J011289);福建省自然科学基金资助项目(2023J011471)

The efficacy of double plasma molecular adsorption system in the treatment of patients with HBV-related acute-on-chronic liver failure

ZHANG Dong-qing, LIAO Zi-yuan, LIN Sheng-long, WU Wen-jun, WANG Xiang-mei, MA Hua-xi, GAO Hai-bing   

  1. Department of Severe Hepatology,Mengchao Hepatobiliary Hospital of Fujian Medical University,Fuzhou 350028,China
  • Received:2023-11-30 Online:2025-01-31 Published:2025-03-10
  • Contact: GAO Hai-bing,Email:gaohb605@163.com

摘要: 目的 探讨双重血浆分子吸附系统(DPMAS)与单纯血浆置换(PE)换在HBV相关慢加急性肝衰竭患者中的疗效。 方法 回顾性收集2022年9月—2023年1月于福建医科大学孟超肝胆医院住院的HBV相关慢加急性肝衰竭患者40例,根据患者所接受的人工肝模式分为A组为DPMAS治疗组,B组为PE组,两组各20例。收集患者治疗前后包括血常规、生化指标、凝血功能、炎症指标等临床指标以及患者并发症发生情况,并计算治疗前MELD值及MELD-Na值。所有入组患者随访3个月,比较观察期内的病情进展、实验室指标变化和无肝移植存活率。 结果 两组患者人工肝治疗前性别、年龄、病情分期、并发症发生情况、临床指标、MELD评分及MELD-Na评分差异均无统计学意义(P值>0.05)。两组人工肝治疗模式,患者3个月的无肝移植存活率分别为:DPMAS组80%,PE组70%,两组间差异无统计学意义。 治疗后24 h,两组患者总胆红素(TBil)、直接胆红素(DBil)均较前显著下降,DPMAS组治疗前后TBil分别为362.2(302.8, 443.1)、263.0(219.9, 349.2)μmol/L(Z=-3.003,P=0.003);DBil分别为180.6(154.7, 222.3)、127.6(112.0, 178.7)μmol/L(Z=-2.867,P=0.004);PE组治疗前后TBil分别为(419.2±147.0)、(339.7±113.3)μmol/L(t=1.914,P=0.063);DBil分别为(202.9±59.3)、(164.5±48.1)μmol/L,t=2.254,P=0.030;与PE治疗组相比,DPMAS治疗组TBil、DBil下降率更高,分别为TBil:(25.6±8.3)、(17.9±7.4)μmol/L(t=3.090,P=0.004);DBil:(25.7±9.2)、(18.4±8.1)μmol/L(t=2.682,P=0.011);PE治疗组凝血酶原时间(PT)、国际标准化比值(INR)均较前下降,分别为PT:28.6(21.1, 32.7)、21.9(17.7, 24.8)s(Z=-2.489,P=0.013);INR:2.7(1.9, 3.2)、1.9(1.4, 2.2)(Z=-2.462,P=0.014);凝血酶原活动度(PTA)较前升高,分别为(31.2±11.1)%、(42.7±13.7)%(t=-2.918,P=0.006),差异均具有统计学意义;DPMAS治疗组在治疗前后凝血指标无显著差异;PE治疗组白蛋白(Alb)较前显著升高,分别为29.5(27.3, 33.8)、32.0(30.3, 35.0)g/L(Z=-2.025,P=0.043);DPMAS组治疗前后Alb无显著差异;DPMAS组治疗后C反应蛋白(CRP)均较前显著下降,分别为11.8(7.1, 21.4)、8.0(5.4, 12.0)mg/L(Z=-2.002,P=0.045);PE组治疗前后CRP无统计学差异。4.治疗后72 h:DPMAS治疗组TBil、DBil仍较治疗前显著下降TBil:362.2(302.8, 443.1)、297.8(213.4, 394.6)μmol/L,Z=-2.110,P=0.035;DBil:180.6(154.7, 222.3)、143.8(102.8, 184.9)μmol/L,Z=-2.218,P=0.027;PE治疗组TBil、DBil治疗前后差异无统计学意义;两组治疗前后凝血功能差异均无统计学意义;PE组治疗后血红蛋白(Hb)较前显著下降,分别为(121.4±14.0)、(111.3±12.3)g/L(t=2.423,P=0.020);DPMAS组治疗前后Hb无显著差异。DPMAS治疗组患者与PE治疗组患者3个月无肝移植存活率无统计学差异。 结论 DPMAS治疗模式对于胆红素以及CRP等炎症介质的清除优于PE模式;DPMAS治疗模式对凝血功能无明显影响。

关键词: 双重血浆分子吸附系统, 血浆置换, 乙型肝炎病毒, 肝功能衰竭, 疗效

Abstract: Objective To investigate the efficacy of double plasma molecular adsorption system (DPMAS) and plasma exchange (PE) in patients with HBV-related acute-on-chronic liver failure. Methods Forty patients with HBV-related acute-on-chronic liver failure who were hospitalized in Mengchao Hepatobiliary Hospital of Fujian Medical University from September 2022 to January 2023 were retrospectively collected. The patients were divided into a DPMAS treatment group (group A) and a PE treatment group (group B), with 20 cases in each group. The clinical indicators including blood routine, biochemical indicators, coagulation function, inflammatory indicators and the occurrence of complications were collected before and after treatment, and the MELD value and MELD-Na value before treatment were calculated. All patients were followed up for 3 months. The disease progression, laboratory parameters and liver transplantation-free survival rate during the observation period were compared. Methods 1. There were no significant differences in gender, age, disease stage, complications, clinical indicators, MELD score and MELD-Na score between the two groups before artificial liver treatment (P>0.05). 2.The 3-month liver transplantation-free survival rate was 80% in group A and 70% in group B. There was no statistical difference between the two groups. 3. At 24 hours after treatment, the levels of total bilirubin (TBil) and direct bilirubin (DBil) in the two groups decreased, and the difference was statistically significant (Group A:TBil 362.2(302.8, 443.1) vs. 263.0(219.9, 349.2)μmol/L,Z=-3.003,P=0.003;DBil 180.6(154.7, 222.3) vs. 127.6(112.0, 178.7)μmol/L,Z=-2.867,P=0.004;Group B:TBil 419.2±147.0 vs. 339.7±113.3 μmol/L,t=1.914,P=0.063;DBil 202.9±59.3 vs. 164.5±48.1 μmol/L,t=2.254,P=0.030). Compared with group B, the reduction rate of TBil and DBil in group A was higher ( TBil:25.6±8.3 vs. 17.9±7.4 μmol/L,t=3.090,P=0.004;DBil:25.7±9.2 vs. 18.4±8.1 μmol/L,t=2.682,P=0.011). The prothrombin time (PT) and international normalized ratio (INR) in the group B decreased (PT:28.6(21.1, 32.7) vs. 21.9(17.7, 24.8) s,Z=-2.489,P=0.013;INR:2.7(1.9, 3.2) vs. 1.9(1.4, 2.2),Z=-2.462,P=0.014), whereas the prothrombin time activity (PTA) increased (31.2±11.1% vs. 42.7±13.7%,t=-2.918,P=0.006). There was no significant difference in coagulation indexes before and after treatment in group A. Group B had a significant increase in albumin (Alb) [11.8(7.1, 21.4) vs. 8.0(5.4, 12.0)g/L,Z=-2.002,P=0.045], whereas group A had no significant difference in Alb before and after treatment. Group A had a decrease in C-reactive protein (CRP) after treatment, while group B had no significant difference in CRP before and after treatment. 4. At72 hours after treatment: TBil and DBil in DPMAS treatment group continued to decrease and had statistical significance [TBil:362.2(302.8, 443.1) vs. 297.8(213.4, 394.6)μmol/L,Z=-2.110,P=0.035;DBil:180.6(154.7, 222.3) vs. 143.8(102.8, 184.9)μmol/L,Z=-2.218,P=0.027]. While TBil and DBil in group B had no statistical significance before and after treatment; There was no significant difference in coagulation function between the two groups before and after treatment. The patients in group B had a significant reduction in hemoglobin (Hb) before and after treatment (121.4±14 vs. 111.3±12.3 g/L,t=2.423,P=0.020), whereas group A had no significant difference in HB before and after treatment. There was no statistically significant difference in 3-month liver transplantation-free survival rate between group A and group B patients. Conclusion DPMAS is superior to PE in the clearance of bilirubin and inflammatory mediators such as CRP. DPMAS treatment has no significant effect on coagulation function.

Key words: Double plasma molecular adsorption system, Plasma exchange, Hepatitis B virus, Liver failure, Efficacy