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小剂量阿加曲班在连续性肾脏替代治疗中的疗效和安全性分析
引用本文:唐莲,陆灏迪,许晓文,周峰,赵富丽,庄智伟,尚尔宁.小剂量阿加曲班在连续性肾脏替代治疗中的疗效和安全性分析[J].中国医院药学杂志,2018,38(6):626-629,644.
作者姓名:唐莲  陆灏迪  许晓文  周峰  赵富丽  庄智伟  尚尔宁
作者单位:1. 南京医科大学附属苏州医院, 苏州市立医院药学部, 江苏 苏州 215002; 2. 南京医科大学药学院, 江苏 南京 211166; 3. 南京医科大学附属苏州医院, 急诊科, 江苏 苏州 215002; 4. 南京医科大学附属苏州医院, 重症监护室, 江苏 苏州 215002
基金项目:江苏省药学会奥赛康临床药学基金科研项目(编号:201511)
摘    要:目的:探讨小剂量阿加曲班在高出血风险患者行连续性肾脏替代治疗(CRRT)中的抗凝效果以及安全性。方法:入选高出血风险患者给予阿加曲班0.1~0.3μg·(kg·min)-1抗凝,评估凝血指标、滤器管路凝血事件、全身出血事件以及血象和肝功能指标。结果:共入选28例高出血风险患者行CRRT397周期,与CRRT前相比:治疗期间和CRRT结束后0~3h的活化部分凝血活酶时间(APTT)差异有显著性(P=0.000);CRRT结束3h后APTT的差异无显著性。根据CRRT上机2~4h的APTT以及血液净化管路动静脉压情况调整阿加曲班给药剂量共114次,调整剂量后复测APTT较前降低,与CRRT上机2~4h相比,差异有显著性(P=0.034)。CRRT期间发生管路和滤器凝血事件共55周期(13.85%)。阿加曲班抗凝期间发生出血事件6例,其中气道出血3例,皮肤瘀斑2例,消化道出血1例,CRRT期间继续减量使用阿加曲班抗凝未观察到有出血加重事件。结论:APTT与阿加曲班抗凝剂量具有较好的相关性,在CRRT结束后凝血指标较快恢复正常,小剂量阿加曲班对高出血风险患者CRRT期间抗凝治疗具有较好的抗凝效果和安全性。

关 键 词:阿加曲班  小剂量  高出血风险  连续性肾脏替代治疗  凝血指标
收稿时间:2017-04-17

Anticoagulative efficacy and safety of small dose argatroban in continuous renal replacement therapy
TANG Lian,LU Hao-di,XU Xiao-wen,ZHOU Feng,ZHAO Fu-li,ZHUANG Zhi-wei,SHANG Er-ning.Anticoagulative efficacy and safety of small dose argatroban in continuous renal replacement therapy[J].Chinese Journal of Hospital Pharmacy,2018,38(6):626-629,644.
Authors:TANG Lian  LU Hao-di  XU Xiao-wen  ZHOU Feng  ZHAO Fu-li  ZHUANG Zhi-wei  SHANG Er-ning
Institution:1. Department of Pharmacy, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Jiangsu Suzhou 215002, China; 2. College of Pharmacy, Nanjing Medical University, Jiangsu Nanjing 211166, China; 3. Department of Emergency, Jiangsu Suzhou 215002, China; 4. Intensive Care Unit, Jiangsu Suzhou 215002, China
Abstract:OBJECTIVE To investigate the anticoagulative efficacy and safety of argatroban in patients with high risk of bleeding receiving continuous renal replacement therapy (CRRT).METHODS Patients with high risk of bleeding received argatroban 0.1-0.3 μg·(kg·min)-1 during CRRT therapy. Coagulation parameters, clotting events, systemic bleeding events were evaluated for the anticoagulative efficacy and safety of argatroban. RESULTS Twenty eight cases with high risk of bleeding received CRRT totally for 397 cycles. Compared to that before CRRT, activated partial thromboplastin times (APTT) during CRRT and 3 h after CRRT had significant differences. No difference was found between the values before and 3h after CRRT. According to APTT at 2-4 h after starting CRRT and blood purification tube arteriovenous pressure, argatroban dose had been adjusted for 114 times. APTT after dose adjustment was decreased and showed significant difference compared to APTT at 2-4 h after starting CRRT (P=0.034). The incidence of coagulation within the filter and/or the pipeline in the argatroban anticoagulation was 13.85%(55 cycles). There were 6 cases of bleeding events, including 3 cases of trachea hemorrhage, 2 of skin ecchymosis and 1 of gastrointestinal bleeding. There were no hemorrhage symptoms aggravated at decreased dose of argatroban. CONCLUSION APTT has a close correlation with the dose of argatroban. The coagulation parameters recover quickly after CRRT. Small dose argatroban in high risk bleeding patients receiving CRRT has good effect and high security.
Keywords:argatroban  small dose  high risk of bleeding  CRRT  coagulation parameters  
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