Lane D A, Ireland H, Flynn A, Anastassiades E, Curtis J R
Nephrol Dial Transplant. 1986;1(3):179-87.
We have performed a dose ranging study of a low MW heparin, Kabi 2165, during haemodialysis in humans (n = 16) and compared it to a dose of unfractionated commercial heparin that has already been shown to inhibit fibrin formation. Low MW heparin administered as 5000 or 10,000 anti-factor Xa units, s.c., half an hour prior to the initiation of dialysis was unable to prevent fibrin formation in the dialyser circuit. A single bolus injection of 5000 anti-factor Xa units of low MW heparin given i.v. inhibited fibrin formation, as determined by FPA generation, for up to 4 h and permitted dialysis for 6 h. Such a bolus injection may be useful for short frequent dialyses. Infusion of low MW heparin in the same dosage regimen as unfractionated heparin, 5000 anti-factor Xa units bolus plus 1500 anti-factor Xa units/h, resulted in a progressive rise in heparin, caused by its longer half-life of elimination from the circulation, and almost completely suppressed both FPA generation and fibrin clot formation for 6 h dialysis. From these studies we calculate that infusion of this low MW heparin at a dose of approximately 4000 anti-factor Xa units bolus plus 750 anti-factor Xa units/h should be a useful regimen that will be effective in suppressing fibrin formation during prolonged dialysis, and the plasma anti-factor Xa level of low MW heparin may reflect its ability to inhibit fibrin formation, although exactly comparable anti-factor Xa levels of unfractionated commercial heparin and low MW heparins may not have identical inhibitory effects.
我们对一种低分子量肝素(卡比2165)在人体血液透析过程中进行了剂量范围研究(n = 16),并将其与已被证明能抑制纤维蛋白形成的普通商业肝素剂量进行了比较。在透析开始前半小时皮下注射5000或10000抗Xa因子单位的低分子量肝素,无法防止透析器回路中纤维蛋白的形成。静脉注射5000抗Xa因子单位的低分子量肝素单次推注可抑制纤维蛋白形成,通过纤维蛋白肽A生成测定,长达4小时,并允许进行6小时的透析。这种推注可能对短时间频繁透析有用。以与普通肝素相同的剂量方案输注低分子量肝素,即5000抗Xa因子单位推注加1500抗Xa因子单位/小时,由于其从循环中消除的半衰期较长,导致肝素水平逐渐升高,并且在6小时透析期间几乎完全抑制了纤维蛋白肽A的生成和纤维蛋白凝块的形成。从这些研究中我们计算出,以大约4000抗Xa因子单位推注加750抗Xa因子单位/小时的剂量输注这种低分子量肝素应该是一种有用的方案,在长时间透析期间能有效抑制纤维蛋白形成,并且低分子量肝素的血浆抗Xa水平可能反映其抑制纤维蛋白形成的能力,尽管普通商业肝素和低分子量肝素的抗Xa水平完全可比时可能没有相同的抑制作用。