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低分子量肝素依诺肝素在血液透析中的剂量探索性研究。

Dose finding study of a low molecular weight heparin, Innohep, in haemodialysis.

作者信息

Ryan K E, Lane D A, Flynn A, Shepperd J, Ireland H A, Curtis J R

机构信息

Department of Haematology, Charing Cross and Westminster Medical School, London, UK.

出版信息

Thromb Haemost. 1991 Sep 2;66(3):277-82.

PMID:1745997
Abstract

A pilot investigation was performed with Innohep, a low molecular weight (LMWH) preparation (peak maximum molecular mass 3,000-6,000), to determine possible dose regimens for patients undergoing regular maintenance haemodialysis for chronic renal failure. Results from this study suggested that suppression of macroscopic clot formation and fibrinopeptide A (FPA), a marker of fibrin formation, could be achieved following bolus injections rather than bolus injections and an infusion. On the basis of these preliminary findings, a randomised crossover study was performed in eight patients undergoing regular maintenance haemodialysis for 5-7 h to determine the effective antithrombotic dose of this LMWH. Single i.v. bolus doses of 1,250 AFXa u, 2,500 AFXa u and 5,000 AFXa u (n = 7-8) were compared to an UFH regime of 5,000 iu + 1,500 iu/h. Excessive clot formation in the dialyser bubble trap, necessitating additional UFH to enable completion of a prolonged (up to 7 h) dialysis, was observed in all patients on the 1,250 AFXa u dose (mean duration of dialysis prior to UFH, 3 h) but in a single patient only receiving the other LMWH doses. A dose-related response in the AFXa activity, measured by chromogenic substrate (CS) assay was seen in the three LMWH groups, with levels declining significantly (p less than 0.05) from 1-7 h. This contrasted with the constant levels maintained during dialysis with UFH. FPA levels were significantly elevated after 2 h following the 1,250 AFXa u bolus and after 4 h following the 2,500 AFXa u bolus. There was no significant difference in FPA levels between the 5,000 AFXa u bolus and UFH.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用低分子量(LMWH)制剂依诺肝素(峰值最大分子量3000 - 6000)进行了一项初步研究,以确定慢性肾衰竭定期维持性血液透析患者的可能给药方案。该研究结果表明,推注给药而非推注加输注给药后,可抑制肉眼可见的凝块形成以及纤维蛋白形成标志物纤维蛋白肽A(FPA)。基于这些初步发现,对8名进行5 - 7小时定期维持性血液透析的患者进行了一项随机交叉研究,以确定该LMWH的有效抗血栓剂量。将1250抗Xa国际单位、2500抗Xa国际单位和5000抗Xa国际单位的单次静脉推注剂量(n = 7 - 8)与5000国际单位 + 1500国际单位/小时的普通肝素(UFH)方案进行比较。在接受1250抗Xa国际单位剂量的所有患者(在使用UFH之前的平均透析时间为3小时)中,但仅在一名接受其他LMWH剂量的患者中,观察到透析器气泡捕集器中形成过多凝块,需要额外使用UFH才能完成延长(长达7小时)的透析。通过发色底物(CS)测定法测量,在三个LMWH组中观察到抗Xa活性的剂量相关反应,从1 - 7小时水平显著下降(p小于0.05)。这与使用UFH透析期间维持的恒定水平形成对比。在1250抗Xa国际单位推注后2小时和2500抗Xa国际单位推注后4小时,FPA水平显著升高。5000抗Xa国际单位推注和UFH之间的FPA水平无显著差异。(摘要截短于250字)

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