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两种血液透析膜(聚丙烯腈和醋酸纤维素)对补体和凝血系统影响的比较

Comparison of two hemodialysis membranes, polyacrylonitrile and cellulose acetate, on complement and coagulation systems.

作者信息

Moll S, De Moerloose P, Reber G, Schifferli J, Leski M

机构信息

Department of Medicine, University Cantonal Hospital, Geneva, Switzerland.

出版信息

Int J Artif Organs. 1990 May;13(5):273-9.

PMID:2142140
Abstract

Two hemodialysis membranes, polyacrilonitrile (AN 69) and cellulose acetate (CA), were compared for their effects on complement and hemostasis. Two groups of 5 patients, in dialysis for more than 5 years, were successively dialysed for 4 weeks periods with each type of membrane. We measured C3a (complement activation), platelets and beta-thromboglobulin (platelet activation), thrombin-antithrombin III complexes and fibrinopeptide A (coagulation activation), using C-Reactive Protein as a control for dilution effects. As previously shown, activation of complement was more important with CA than with AN 69 (p less than 0.01). In contrast, activation of coagulation (increase in fibrinopeptide A and thrombin-antithrombin III complexes) was more pronounced with AN 69 than with CA. This study emphasizes the need to consider different biological systems when the bioincompatibility of a hemodialysis membrane is evaluated.

摘要

比较了两种血液透析膜,即聚丙烯腈(AN 69)和醋酸纤维素(CA)对补体和止血的影响。两组各5名透析超过5年的患者,先后使用每种类型的膜进行为期4周的透析。我们检测了C3a(补体激活)、血小板和β-血小板球蛋白(血小板激活)、凝血酶-抗凝血酶III复合物和纤维蛋白肽A(凝血激活),使用C反应蛋白作为稀释效应的对照。如先前所示,CA引起的补体激活比AN 69更显著(p<0.01)。相反,AN 69引起的凝血激活(纤维蛋白肽A和凝血酶-抗凝血酶III复合物增加)比CA更明显。这项研究强调,在评估血液透析膜的生物不相容性时,需要考虑不同的生物系统。

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引用本文的文献

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Cellulose, modified cellulose and synthetic membranes in the haemodialysis of patients with end-stage renal disease.纤维素、改性纤维素及合成膜在终末期肾病患者血液透析中的应用
Cochrane Database Syst Rev. 2005 Jul 20;2005(3):CD003234. doi: 10.1002/14651858.CD003234.pub2.
2
Complement activation and bioincompatibility. The terminal complement complex for evaluation and surface modification with heparin for improvement of biomaterials.补体激活与生物不相容性。用于评估的末端补体复合物以及用肝素进行表面修饰以改善生物材料。
Clin Exp Immunol. 1991 Oct;86 Suppl 1(Suppl 1):21-6.