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Dialysis Unphysiology and Sodium Balance

机译:透析生理异常与钠平衡

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摘要

Dialysis unphysiology was first discussed by Carl Kjellstrand in 1975 for the possible negative effects of the unphysiology of intermittent dialysis treatment. Current hemodialysis practices are still unphysiologic because they cannot keep blood chemistries within normal limits, both before and after dialysis. In addition, the discontinuous nature of hemodialysis causes saw-tooth volume fluctuations, and the extracellular fluid volume expansion during the interdialytic period may lead to hypertension and adverse cardiovascular consequences. Sodium, which is accumulated over the interdialytic period, may be divided into two fractions. The one is the fraction of osmotically active sodium which is mainly confined to the extracellular space, and the other is that of water-free (osmotically inactive) sodium which diffuses into the intracellular space. Both contribute to the pathogenesis of hypertension because the former may act to expand extracellular fluid volume and the latter may cause vasoconstriction in the long run by increasing cytosolic concentration of calcium in the vascular smooth muscle cells. Even in intensive hemodialysis, it may take several weeks to months for water-free sodium storage in the vascular smooth muscle cells to be relieved. This may be an explanation for the lag phenomenon, i.e., the delay of blood pressure decrease after normalization of extracellular fluid volume shown in the Tassin experience. Modest restriction of dietary sodium intake, the dialytic session length long enough to maintain a high ultrafiltration volume, and the reasonably low dialysate sodium concentration are required to avoid unphysiology of positive sodium balance in current hemodialysis practice.
机译:透析非生理学是1975年由Carl Kjellstrand首次讨论的,涉及间歇性透析治疗的非生理学可能产生的负面影响。当前的血液透析实践仍然是不生理的,因为它们不能在透析前后将血液化学性质保持在正常范围内。另外,血液透析的不连续性导致锯齿形的体积波动,并且在透析间隔期间细胞外液的体积膨胀可能导致高血压和不利的心血管后果。在渗析期间累积的钠可分为两部分。一个是渗透活性钠的一部分,主要限于细胞外空间,另一部分是无水(渗透惰性)的钠,其扩散到细胞内空间。两者均与高血压的发病机理有关,因为前者可能通过增加血管平滑肌细胞中钙的胞浆浓度而长期起到扩大细胞外液体积的作用,而后者可能引起血管收缩。即使在进行密集的血液透析时,也可能需要数周至数月才能缓解血管平滑肌细胞中无水钠的储存。这可能是滞后现象的一种解释,即,Tassin经验中所示的细胞外液量正常化后,血压下降的延迟。饮食中钠的摄入量应适度限制,透析时间应足够长以维持高超滤量,并且透析液中的钠浓度应合理低一些,以避免当前血液透析中钠平衡失衡的生理现象。

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