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持续性非卧床腹膜透析中低钙透析液与口服碳酸钙:一种在尽量减少铝暴露和高钙血症的同时控制高磷血症的方法。

Low-calcium dialysis fluid and oral calcium carbonate in CAPD. A method of controlling hyperphosphataemia whilst minimizing aluminium exposure and hypercalcaemia.

作者信息

Hutchison A J, Freemont A J, Boulton H F, Gokal R

机构信息

Manchester Royal Infirmary Renal Unit, University of Manchester, UK.

出版信息

Nephrol Dial Transplant. 1992;7(12):1219-25. doi: 10.1093/ndt/7.12.1219.

Abstract

Oral calcium carbonate is an effective phosphate binder in dialysis patients. Its use minimizes aluminium intake, and by maintaining a high-normal serum ionized calcium, suppresses serum parathyroid hormone levels. However, the dose required to control hyperphosphataemia may cause hypercalcaemia. We performed prospective studies in 50 previously undialysed patients starting CAPD (28 study group, 22 control group). Calcium carbonate was the only phosphate binder used in the study group which utilized a low calcium PD fluid (calcium 1.25 mmol/l), whilst the control group used standard PD solution (calcium 1.75 mmol/l) with calcium carbonate plus aluminium hydroxide phosphate binders as clinically indicated. The study group was able to take larger doses of oral calcium carbonate with no increase in episodes of hypercalcaemia compared to the control group. There were no instances of hypocalcaemia in any patient using the low-calcium dialysis fluid. Phosphate control was better in the study group, despite the additional use of aluminium-containing phosphate binders by some patients in the control group. Serum aluminium levels in the study group were maintained at < 11.5 mumol/l, but increased significantly in the control group from 3 months onward. Mean serum parathyroid hormone in the study group declined significantly from baseline values over the first 6 months, and remained at the lower level. Bone histology showed a tendency towards improvement over the 12 months, in terms of osteoclast numbers and activity. We conclude that using dialysis fluid with a reduced calcium concentration in compliant, well-monitored patients is safe.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

口服碳酸钙是透析患者有效的磷结合剂。其使用可使铝摄入量降至最低,并通过维持血清离子钙处于高正常水平来抑制血清甲状旁腺激素水平。然而,控制高磷血症所需的剂量可能会导致高钙血症。我们对50名开始进行持续性非卧床腹膜透析(CAPD)的未透析患者进行了前瞻性研究(28名研究组患者,22名对照组患者)。研究组仅使用碳酸钙作为磷结合剂,采用低钙腹膜透析液(钙1.25 mmol/L),而对照组使用标准腹膜透析液(钙1.75 mmol/L),并根据临床指征使用碳酸钙加氢氧化铝磷结合剂。与对照组相比,研究组能够服用更大剂量的口服碳酸钙,且高钙血症发作次数未增加。使用低钙透析液的任何患者均未出现低钙血症情况。尽管对照组一些患者额外使用了含铝磷结合剂,但研究组的磷控制效果更好。研究组血清铝水平维持在<11.5 μmol/L,但对照组从3个月起显著升高。研究组的平均血清甲状旁腺激素在最初6个月内从基线值显著下降,并维持在较低水平。骨组织学显示,在破骨细胞数量和活性方面,12个月内有改善趋势。我们得出结论,在依从性好、监测良好的患者中使用钙浓度降低的透析液是安全的。(摘要截短至250字)

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