Silver S M, Sterns R H, Halperin M L
Department of Medicine/Nephrology Unit, University of Rochester School of Medicine, Rochester General Hospital, Rochester, NY 14621, USA.
Am J Kidney Dis. 1996 Jul;28(1):1-13. doi: 10.1016/s0272-6386(96)90124-9.
The pathogenesis of brain swelling and neurological deterioration after rapid hemodialysis (dialysis disequilibrium syndrome) is controversial. The "reverse urea hypothesis" suggests that hemodialysis removes urea more slowly from the brain than from the plasma, creating an osmotic gradient that results in cerebral edema. The "idiogenic osmole hypothesis" proposes that an osmotic gradient between brain and plasma develops during rapid dialysis because of newly formed brain osmoles. In this review, the experimental basis for the two hypotheses are critically examined. Based on what is known about the physiology of urea and water diffusion across the blood-brain barrier, and empiric observations of brain solute composition after experimental hemodialysis, we conclude that the "reverse urea hypothesis" remains a viable explanation for dialysis disequilibrium and that rapid reduction of a high urea level in and of itself predisposes to this condition.
快速血液透析后出现脑肿胀和神经功能恶化(透析失衡综合征)的发病机制存在争议。“反向尿素假说”认为,血液透析从大脑中清除尿素的速度比从血浆中清除的速度慢,从而形成渗透梯度,导致脑水肿。“内源性渗透物质假说”提出,在快速透析过程中,由于新形成的脑渗透物质,大脑和血浆之间会形成渗透梯度。在本综述中,对这两种假说的实验依据进行了严格审查。基于对尿素和水跨血脑屏障扩散生理学的了解,以及实验性血液透析后脑溶质组成的经验性观察,我们得出结论,“反向尿素假说”仍然是透析失衡的一个可行解释,并且快速降低高尿素水平本身就易引发这种情况。