Stefoni Sergio, Cianciolo Giuseppe, Donati Gabriele, Colì Luigi, La Manna Gaetano, Raimondi Concettina, Dalmastri Vittorio, Orlandi Valentina, D'Addio Franesca
Nephrology Dialysis and Renal Transplantation Unit, Department of Clinical Medicine and Applied Biotechnology, S. Orsola University Hospital, Bologna, Italy.
Nephron. 2002;92(3):589-600. doi: 10.1159/000064086.
To compare standard heparin (SH) and low molecular weight heparin (LMWH) in terms of anticoagulation, platelet activation and lipid metabolism, we selected 54 patients who had been on 4-hour hemodialysis three times weekly for at least 12 months, without bleeding disorders or dyslipidemic diseases. 28 were on hemodialysis with Polysulfone low-flux, 26 were on hemodiafiltration with Polysulfone high-flux. All patients underwent EPO.
During the first 18 months, we administered SH 1,500 IU on starting dialysis and 1,500 +/- 500 IU in continuous intradialytic infusion per session. In the following 18 months, we administered LMWH 64.6 IU/kg on starting dialysis in a single arterious bolus. We assessed aPTT, anti-factor Xa activity, TAT and FPA, beta-TG and PF4. Blood samples were taken monthly at times 0, 30, 60, 180 and 240 min, as well as 1, 4 and 20 h after dialysis end. Predialysis cholesterol, HDL, LDL, triglycerides and lipoprotein(a) were checked monthly.
During both LMWH and SH sessions no clotting or major bleeding complications were observed. APTT with LMWH was lower than that found with SH (p < 0.001); aFXa using LMWH was higher than when using SH (p < 0.001); TAT and FPA were lower in LMWH sessions (p < 0.01) than in SH sessions. We also detected lower beta-TG (p < 0.05) and PF4 levels (p < 0.05) using LMWH than using SH. As regards lipids, we only observed a significant decrease in triglycerides after 18 months of LMWH treatment.
Routine use of LMWH during hemodialysis affords a safe and effective alternative to SH, and causes reduced platelet activation.
为了比较标准肝素(SH)和低分子量肝素(LMWH)在抗凝、血小板活化和脂质代谢方面的差异,我们选择了54例每周进行3次4小时血液透析至少12个月、无出血性疾病或血脂异常疾病的患者。28例使用聚砜低通量进行血液透析,26例使用聚砜高通量进行血液透析滤过。所有患者均接受促红细胞生成素(EPO)治疗。
在最初的18个月里,我们在透析开始时给予SH 1500 IU,每次透析过程中持续静脉内输注1500±500 IU。在接下来的18个月里,我们在透析开始时通过单次动脉推注给予LMWH 64.6 IU/kg。我们评估了活化部分凝血活酶时间(aPTT)、抗Xa因子活性、凝血酶-抗凝血酶复合物(TAT)和纤维蛋白肽A(FPA)、β-血小板球蛋白(β-TG)和血小板第4因子(PF4)。每月在0、30、60、180和240分钟时以及透析结束后1、4和20小时采集血样。每月检查透析前胆固醇、高密度脂蛋白(HDL)、低密度脂蛋白(LDL)、甘油三酯和脂蛋白(a)。
在LMWH和SH治疗期间均未观察到凝血或严重出血并发症。LMWH治疗时的aPTT低于SH治疗时(p<0.001);使用LMWH时的抗Xa因子活性高于使用SH时(p<0.001);LMWH治疗期间的TAT和FPA低于SH治疗期间(p<0.01)。我们还检测到使用LMWH时的β-TG水平(p<0.05)和PF4水平(p<0.05)低于使用SH时。关于脂质,我们仅观察到LMWH治疗18个月后甘油三酯有显著下降。
血液透析期间常规使用LMWH是SH的一种安全有效的替代方法,并且可减少血小板活化。