肝脏 ›› 2025, Vol. 30 ›› Issue (2): 231-235.

• 其他肝病 • 上一篇    下一篇

甲磺酸萘莫司他与普通肝素在双重血浆分子吸附系统治疗中的抗凝作用

王新月, 周莉, 陈煜   

  1. 100069 北京 首都医科大学附属北京佑安医院肝病中心四科 肝衰竭与人工肝治疗研究北京市重点实验室
  • 收稿日期:2024-08-13 出版日期:2025-02-28 发布日期:2025-03-17
  • 通讯作者: 陈煜,Email: chybeyond1071@ccmu.edu.cn
  • 基金资助:
    高层次公共卫生技术人才建设项目资助(学科带头人-01-12);北京市医院管理中心“登峰”计划专项经费资助(DFL20221501);双重血浆分子吸附系统(DPMAS)治疗萘莫司他抗凝方案初探的研究(iGandanF-1082022-RGG055)

Case-control study on the efficacy and safety of nafamostat mesylate and heparin in double plasma molecular absorption system

WANG Xin-yue, Zhou Li, CHEN Yu   

  1. Beijing Municipal Key Laboratory of Liver Failure and Artificial Liver Treatment Research, Fourth Department of Liver Diseases, You' an Hospital, Affiliated to Capital Medical University, Beijing 100069, China
  • Received:2024-08-13 Online:2025-02-28 Published:2025-03-17
  • Contact: CHEN Yu, Email: chybeyond1071@ccmu.edu.cn

摘要: 目的 探讨甲磺酸萘莫司他(NM)与肝素(HP)在双重血浆分子吸附系统(DPMAS)治疗中的抗凝效果。方法 选择2022年4月至2024年3月于首都医科大学附属北京佑安医院诊治的高胆红素血症患者103例,在接受DPMAS治疗过程中,分别应用NM或HP体外抗凝。收集患者DPMAS治疗前后TBil、PLT计数、凝血酶原活动度(PTA)及活化部分凝血活酶时间(APTT)等实验室指标和治疗过程中各种压力参数、报警情况、出血或堵管等并发症情况。结果 103例患者中102例顺利完成治疗, HP组1例患者因抗凝不足发生严重堵管而导致治疗中断。NM组抗凝良好率为88.2%(45/51),显著高于HP组的37.3%(19/51);抗凝过量率为3.9%(2/51),显著低于HP组的58.8%(30/51)(P<0.05)。治疗过程中,NM组体外循环管路静脉端APTT与动脉端APTT差值显著大于HP组,为247(110, 286.3)比0. 0(0. 0, 55.5) s(P<0. 05);NM组患者治疗前后血清TBil、Alb和PLT计数差值分别为(164.8±62.6)μmol/L、5.7 (4.7, 7.8)g/L和21.0 (11.5, 33.5)×109/L, HP组分别为(174.3±64.9)μmol/L、6.5 (5.1,8.7)g/L和15(6,24)×109/L,差异无统计学意义(P>0.05)。在治疗过程中,HP组出现严重堵管1例,颈内静脉置管处渗血1例,NM组出现跨膜压和静脉压短时间内上升或机器频繁发生凝血警报4例,颈内静脉置管处渗血1例。结论 在行DPMAS治疗过程中,应用NM体外抗凝效果较HP更佳,安全性更高,但对于PTA≤40%患者,NM的最佳剂量值得进一步探讨。

关键词: 肝衰竭, 双重血浆分子吸附系统, 甲磺酸萘莫司他, 肝素

Abstract: Objective This case-control study was conducted to compare the anticoagulant efficacy and safety of nafmostat mesylate (NM) and heparin (HP) during double plasma molecular absorption system (DPMAS) treatment. Methods 103 patients with hyperbilirubinemia were included in You'an Hospital affiliated to Capital Medical University between April 2022~March 2024 using prospective case-control research methods, and were divided into NM group and HP group with NM or HP in vitro anticoagulation during DPMAS treatment. Laboratory indicators, including total bilirubin (TBil), platelet(PLT) count, prothrombin activity(PTA) and partial thromboplastin time (APTT)were collected before and after DPMAS treatment, and complications such as various pressure parameters, alarms, bleeding or blockage during treatment. Results Out of the 103 DPMAS treatments, the procedure successfully completed in 102(99. 0% ), with only one treatment being discontinued because of plugged pipes induced by insufficient anticoagulation of HP; the satisfactory anticoagulation rate in NM-managed group was 88.2%, significantly higher than the 37.3% observed in HP-intervened group, and the over anticoagulation rate was 3.9%, much lower than the 58.8%(P<0.05) observed in HP-intervened group; During the treatment, the difference between the APTT at the venous and arterial end of the cardiopulmonary bypass line in the NM group [247(110, 286.3) vs. 0.0(0. 0, 55.5) s, P<0.05] significantly larger than the HP group; there were no significant differences in serum bilirubin, albumin levels and platelet counts between the two groups [(164.8±62.6) μmol/L, 5.7 (4.7, 7.8) g/L and 21 (11.5, 33.5) ×109/L, vs. (174.3±64.9) μmol/L, 6.5 (5.1, 8.7) g/L and 15 (6, 24) ×109/L, respectively, P>0.05]; During the course of treatment, severe pipe blockage was found in 1 case in HP anticoagulant group , the puncture skin haemorrhage was observed in 1 case in HP anticoagulant group, 1 case in the NM group, and transient increased transmembrane pressure, or venous pressure or coagulation alert by the machine occurred in 4 cases in NM anticoagulant group. Conclusion In the process of DPMAS treatment, NM demonstrates a better anticoagulation effect and higher safety compared to HP, which is worthy of further discussion. However, for patients with PTA≤40%, the optimal dose of NM requires further investigation.

Key words: Liver failure, Double plasma molecular absorption system, Nafamostat mesylate, Heparin