Sakai Yukinao, Otsuka Tomoyuki, Ohno Dai, Murasawa Tsuneo, Sakai Saori, Tsuruoka Shuichi
Division of Nephrology, Department of Internal Medicine, Nippon Medical School Musashikosugi Hospital, Kawasaki, Japan.
Ther Apher Dial. 2014 Apr;18(2):181-4. doi: 10.1111/1744-9987.12099.
Because active vitamin D preparations and calcimimetics have been widely used to treat secondary hyperparathyroidism, maintenance of acceptable serum calcium and phosphate levels is important. A 2.75 mEq/L dialysate calcium product, which may bring the calcium balance closer to 0, has recently been launched, and we had an opportunity to examine its possible benefits. We performed a 6-month retrospective review after switching from 3.0 mEq/L to 2.75 mEq/L calcium dialysate in 85 outpatients undergoing chronic hemodialysis. We evaluated blood biochemical parameters, including predialysis and postdialysis serum calcium and phosphate levels, predialysis intact parathyroid hormone (iPTH) levels; dialysis dose (Kt/V); and doses of concomitant active vitamin D preparations, calcimimetics, phosphate binder, and erythropoiesis-stimulating agents. Postdialysis calcium levels were significantly lower and predialysis corrected calcium levels significantly decreased. The change in calcium levels before and after dialysis was smaller after switching of the dialysate than before. iPTH levels significantly increased 1 month after switching of the dialysate. No remarkable changes were observed in phosphate levels or Kt/V. The dose of alfacalcidol, one of the concomitant drugs, somewhat increased, and no remarkable changes in dosage were observed for other concomitant drugs. These results were favorable in terms of calcium balance. However, there may be limitations in interpreting the results, but the resultant calcium levels suggest that switching to 2.75 mEq/L calcium dialysate may improve the control of calcium levels. In addition, it is hoped that the treatment choice of secondary hyperparathyroidism is extended.
由于活性维生素D制剂和拟钙剂已被广泛用于治疗继发性甲状旁腺功能亢进,维持可接受的血清钙和磷水平很重要。一种2.75 mEq/L的透析液钙产品最近已推出,其可能使钙平衡更接近零,我们有机会研究其潜在益处。我们对85例接受慢性血液透析的门诊患者从3.0 mEq/L钙透析液转换为2.75 mEq/L钙透析液后进行了为期6个月的回顾性研究。我们评估了血液生化参数,包括透析前和透析后血清钙和磷水平、透析前完整甲状旁腺激素(iPTH)水平;透析剂量(Kt/V);以及活性维生素D制剂、拟钙剂、磷结合剂和促红细胞生成素的伴随使用剂量。透析后钙水平显著降低,透析前校正钙水平显著下降。透析液转换后透析前后钙水平的变化比之前更小。透析液转换1个月后iPTH水平显著升高。磷水平或Kt/V未观察到显著变化。伴随药物之一阿法骨化醇的剂量略有增加,其他伴随药物的剂量未观察到显著变化。这些结果在钙平衡方面是有利的。然而,在解释结果时可能存在局限性,但最终的钙水平表明转换为2.75 mEq/L钙透析液可能改善钙水平的控制。此外,希望能扩展继发性甲状旁腺功能亢进的治疗选择。