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无镁透析液对持续性非卧床腹膜透析期间镁代谢的影响。

Effects of a magnesium-free dialysate on magnesium metabolism during continuous ambulatory peritoneal dialysis.

作者信息

Shah G M, Winer R L, Cutler R E, Arieff A I, Goodman W G, Lacher J W, Schoenfeld P Y, Coburn J W, Horowitz A M

机构信息

Nephrology Section (III N), VA Medical Center, Long Beach, CA 90822.

出版信息

Am J Kidney Dis. 1987 Oct;10(4):268-75. doi: 10.1016/s0272-6386(87)80021-5.

Abstract

While the use of magnesium-containing compounds is usually contraindicated in dialysis patients, the risk of toxicity from hypermagnesemia can be reduced by lowering the magnesium concentration in dialysate. We examined the effects of a magnesium-free dialysate on both serum magnesium level and the peritoneal removal rate of magnesium over 12 weeks in 25 stable patients undergoing continuous ambulatory peritoneal dialysis (CAPD). After 2 weeks, the serum magnesium level decreased from 2.2 to 1.9 mg/dL (0.9 to 0.8 mmol/L) (P less than .02) and the peritoneal removal rate increased from 66 to 83 mg/d (2.8 to 3.5 mmol/d) (P less than .05), with both values remaining stable thereafter. There was a strong association between these parameters (r = -0.62, P less than .05), suggesting that the serum magnesium level decreased as a result of the initial increased peritoneal removal rate. For an additional 4-week period, a subgroup of nine patients received magnesium-containing, phosphate binding agents instead of those containing only aluminum. During this phase, serum inorganic phosphorus was well controlled. The serum magnesium level increased only from 1.8 to 2.5 mg/dL (0.7 to 1.0 mmol/L) (P less than .05), due in great part to the concomitant 41% rise in peritoneal magnesium removal from 91 to 128 mg/d (3.8 to 5.3 mmol/d) (P less than .05). No toxicity was noted during the entire 16-week study period, nor did serum calcium change. Thus, serum magnesium levels remained within an acceptable range as magnesium-containing phosphate binders were given through the use of magnesium-free peritoneal dialysate.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

虽然含镁化合物的使用在透析患者中通常是禁忌的,但通过降低透析液中的镁浓度可以降低高镁血症中毒的风险。我们研究了无镁透析液对25例接受持续性非卧床腹膜透析(CAPD)的稳定患者在12周内血清镁水平和腹膜镁清除率的影响。2周后,血清镁水平从2.2降至1.9mg/dL(0.9至0.8mmol/L)(P<0.02),腹膜清除率从66增加至83mg/d(2.8至3.5mmol/d)(P<0.05),此后这两个值均保持稳定。这些参数之间存在很强的相关性(r = -0.62,P<0.05),表明血清镁水平下降是由于最初腹膜清除率增加所致。在另外4周的时间里,9名患者组成的亚组接受了含镁的磷结合剂而非仅含铝的结合剂。在此阶段,血清无机磷得到了很好的控制。血清镁水平仅从1.8升至2.5mg/dL(0.7至1.0mmol/L)(P<0.05),这在很大程度上是由于腹膜镁清除率随之升高了41%,从91增至128mg/d(3.8至5.3mmol/d)(P<0.05)。在整个16周的研究期间未观察到毒性反应,血清钙也未发生变化。因此,通过使用无镁腹膜透析液给予含镁磷结合剂时,血清镁水平仍保持在可接受范围内。(摘要截取自250字)

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