醋酸钙治疗尿毒性高磷血症:碳酸钙的安全替代品。

M Biagini, M Malaguti, R Sicoli, R Capece, A Friggi, G Ciaffi, R Bargagna
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引用次数: 2

摘要

对19例稳定性血液透析伴持续性高磷血症患者应用醋酸钙(CAA)作为磷结合剂的临床疗效进行了评价。所有患者每周透析3次,透析时间固定,透析液钙含量为3.5 mEq/l。在研究开始前一个月,所有患者停止服用钙和维生素D补充剂。在研究的第一阶段,CAA(平均每日剂量2.2 g)服用一个月,然后停药15天。平均血清磷由7.6 +/- 1.4 mg%降至5.8 +/- 0.8 mg% (p < 0.005)。停药15 d后,血清磷均值达到预处理值。然后,患者进入一项长期研究,使用个性化剂量的CAA(1 - 4克/天),其中8人服用α -骨化醇。平均随访5.4 +/- 1.5个月后,血清磷从7.5 +/- 1.1 mg%降至5.6 +/- 1.1 mg% (p < 0.0005),血钙从9.0 +/- 0.7 mg%上升至9.6 +/- 0.6 mg% (p < 0.005)。只有一名患者出现轻度高钙血症。我们的结论是,CAA是一种安全的替代碳酸钙控制尿毒症患者的高磷血症,因为它最有效的磷结合和较少的钙吸收。
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Treatment of uraemic hyperphosphatemia with calcium acetate: a safe alternative to calcium carbonate.

Clinical usefulness of calcium acetate (CAA) as phosphorus binder was assessed in 19 stable hemodialysis patients with persistent hyperphosphatemia. All were dialysed thrice weekly with a constant dialytic schedule and a dialysate calcium of 3.5 mEq/l. One month prior the study beginning all patients stopped assumption of Ca and vitamin D supplements. In the first period of the study CAA (mean daily doses 2.2 g) was administered for one month followed by 15 days of withdrawal. The mean serum phosphorus decreased from 7.6 +/- 1.4 to 5.8 +/- 0.8 mg% (p < 0.005). After 15 days of withdrawal mean serum phosphorus reached the pretreatment value. Then the patients entered a long term study with personalized doses of CAA (between 1 and 4 g/day) and administration in 8 of them of alpha-calcidol. After a mean follow-up period of 5.4 +/- 1.5 months serum phosphorus was reduced from 7.5 +/- 1.1 to 5.6 +/- 1.1 mg% (p < 0.0005) while calcemia increased from 9.0 +/- 0.7 to 9.6 +/- 0.6 mg% (p < 0.005). Only one patient developed mild hypercalcemia. We concluded that CAA is a safe alternative to calcium carbonate for the control of hyperphosphatemia of uraemic patients for the most efficient phosphorus binding and the lesser absorption of calcium.

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