Naumnik Beata, Pawlak Krystyna, Myśliwiec Michał
Department of Nephrology and Transplantation with Dialysis Unit, Medical University, Białystok, Poland.
Thromb Res. 2009 Feb;123(4):631-6. doi: 10.1016/j.thromres.2007.12.014. Epub 2008 Jan 30.
Unfractionated heparin (UFH) and low molecular weight heparin constitute fundamental anticoagulants during hemodialysis (HD). We aimed to investigate the effect of UFH and enoxaparin on plasma levels of prothrombin fragment 1+2 (PF 1+2) and thrombin/antithrombin complex (TAT) as markers of intravascular thrombogenesis during HD.
We enrolled 22 chronic HD patients, who were randomly assigned to either iv enoxaparin (n=11) or UFH (n=11) anticoagulation, and followed prospectively for 12 weeks before crossing over to the alternate therapy for further 12 weeks. Plasma levels of PF 1+2 and TAT were measured by immunoassay at the start, at 10 and 180 min of HD session after each period of evaluation.
The baseline PF 1+2 and TAT levels were comparable under enoxaparin and UFH treatment. PF 1+2 significantly decreased during both UFH (chi(2) ANOVA=9.82, P=0.007) and enoxaparin (chi(2) ANOVA=29.40, P<10(-6)) anticoagulated HD, while over-HD TAT levels changes differed depending on the type of heparin. The switch from enoxaparin to UFH treatment was connected with a significantly higher PF 1+2 after 10 and 180 min as well as higher TAT concentration after 180 min of HD. Only during enoxaparin anticoagulated HD 34% PF 1+2 decrease and TAT levels after 180 min of HD was closely associated with heparin dosage.
Single bolus of enoxaparin ensures efficient and convenient anti-thrombotic protection during HD procedure. Enoxaparin mean dose of 0.67 mg/kg, which is generally lower than manufacturer's instructions, can be recommended for over-dialytic regular use.
普通肝素(UFH)和低分子量肝素是血液透析(HD)期间的基本抗凝剂。我们旨在研究UFH和依诺肝素对血浆凝血酶原片段1 + 2(PF 1+2)水平以及作为HD期间血管内血栓形成标志物的凝血酶/抗凝血酶复合物(TAT)的影响。
我们招募了22名慢性HD患者,将他们随机分配接受静脉注射依诺肝素(n = 11)或UFH(n = 11)抗凝治疗,并进行前瞻性随访12周,之后交叉接受另一种治疗再持续12周。在每个评估期后的HD治疗开始时、10分钟和180分钟,通过免疫测定法测量PF 1+2和TAT的血浆水平。
在依诺肝素和UFH治疗下,基线PF 1+2和TAT水平相当。在UFH(卡方方差分析= 9.82,P = 0.007)和依诺肝素(卡方方差分析= 29.40,P < 10⁻⁶)抗凝的HD过程中,PF 1+2均显著下降,而HD期间TAT水平的变化因肝素类型而异。从依诺肝素转换为UFH治疗与HD 10分钟和180分钟后显著更高的PF 1+2以及180分钟后更高的TAT浓度相关。仅在依诺肝素抗凝的HD期间,HD 180分钟后PF 1+2下降34%且TAT水平与肝素剂量密切相关。
单次推注依诺肝素可确保HD过程中有效且便捷的抗血栓保护。依诺肝素平均剂量0.67 mg/kg通常低于制造商说明,可推荐用于透析期间常规使用。