血液透析膜生物相容性的临床影响
- Author
- Jeffrey S Berns, MD
Jeffrey S Berns, MD
- Editor-in-Chief — Nephrology
- Section Editor — Dialysis
- Professor of Medicine
- Perelman School of Medicine at the University of Pennsylvania
- Section Editor
- Steve J Schwab, MD
Steve J Schwab, MD
- Editor-in-Chief — Nephrology
- Section Editor — Dialysis
- Chancellor
- University of Tennessee Health Science Center
- Deputy Editor
- Alice M Sheridan, MD
Alice M Sheridan, MD
- Deputy Editor — Nephrology
- Assistant Professor of Medicine
- Harvard Medical School
- Translators
- 江薇, 副主任医师
江薇, 副主任医师
- 上海东方医院肾内科
引言
透析膜与血液成分相互作用可能会引发炎症反应,并导致多种远期临床后遗症,临床后遗症部分取决于透析膜生物相容性程度。生物相容性良好的透析膜(biocompatible membrane, BCM)习惯上是指“最小程度地引起接触透析膜的患者发生炎症反应的膜”[1]。 (参见“血液与血液透析膜相互作用涉及的生化机制”)
然而,目前没有检测生物相容性的标准技术。因此,基于所用的检测方法不同,如白三烯的生成或补体激活的程度,不同透析膜生产商对生物相容性的要求有很大差别。
本专题将讨论血液透析膜生物相容性临床影响的相关问题。诸如环氧乙烷和补体激活导致的对血液透析膜的急性反应,将单独讨论。 (参见“对血液透析膜的反应”)
血液透析膜的类型
目前用于制造透析器的透析膜有3种:纤维素膜、改性纤维素膜(substituted cellulose)、合成非纤维素膜。
纤维素膜 — 纤维素主要被制作成铜仿膜(英文为cuprophan或cuprophane),是一种从压棉中获取的多糖膜。铜仿膜是由含大量自由羟基的失水葡萄糖环链组成。铜铵(cupammonium)被主要用于这种膜的制作过程(因此得名),但是也有其他的生产方法。
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