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持续性非卧床腹膜透析中低透析液钙:一项随机对照多中心试验。腹膜透析多中心研究组。

Low dialysate calcium in continuous ambulatory peritoneal dialysis: a randomized controlled multicenter trial. The Peritoneal Dialysis Multicenter Study Group.

作者信息

Weinreich T, Passlick-Deetjen J, Ritz E

机构信息

Department of Nephrology, University of Heidelberg, Germany.

出版信息

Am J Kidney Dis. 1995 Mar;25(3):452-60. doi: 10.1016/0272-6386(95)90108-6.

Abstract

Hypercalcemia is a common complication in continuous ambulatory peritoneal dialysis (CAPD) patients treated with calcium-containing phosphate binders and using the standard dialysate calcium concentration of 3.5 mEq/L (SCa). Lowering the dialysate calcium was proposed to overcome this problem. The current randomized controlled multicenter study was designed to investigate efficiency and safety of a low calcium dialysate (2.00 mEq/L; LCa) compared with SCa (3.5 mEq/L) in CAPD patients. After an 8-week run-in period, 103 stable CAPD patients, 68 men, 35 women, aged 54.5 years (range, 20 to 77)) were randomly allotted to treatment with either LCa or SCa. All patients received calcium carbonate as oral phosphate binder to achieve serum phosphate levels < 6.2 mg/dL. If persistent hypercalcemia arose, CaCO3 was replaced by Al(OH)3 until normocalcemia was achieved. All patients received 0.25 microgram calcitriol/d. Parameters monitored included total and ionized serum calcium, serum phosphate, phosphate binder intake, incidence of hypercalcemia, serum aluminium, intact parathyroid hormone (1,84PTH), osteocalcin, alkaline phosphatase, bone mineral density and hand skeletal x-ray. Primary end points were (a) number of hypercalcemic episodes, (b) tolerated doses of calcium-containing phosphate binders, and (c) 1,84PTH. After 6 months of therapy, total and ionized calcium were lower in LCa patients (total Ca:9.6 v 10.08 mEq/L, P = 0.005; iCa: 4.76 v 5.15 mg/dL; P = 0.013). In the LCa group, significantly fewer episodes of hypercalcemia were recorded (total S-calcium > 10.8 mg/dL: LCa 24 v SCa 86 episodes; P < 0.005). Use of LCa permitted the administration of more CaCO3 (mean daily tablet number: LCa, 5.9 v SCa, 4.2; P < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

高钙血症是接受含钙磷结合剂治疗且使用标准透析液钙浓度3.5 mEq/L(SCa)的持续性非卧床腹膜透析(CAPD)患者的常见并发症。有人提出降低透析液钙浓度以解决这一问题。当前这项随机对照多中心研究旨在调查低钙透析液(2.00 mEq/L;LCa)与SCa(3.5 mEq/L)相比在CAPD患者中的有效性和安全性。经过8周的导入期后,103例稳定的CAPD患者(68例男性,35例女性,年龄54.5岁,范围20至77岁)被随机分配接受LCa或SCa治疗。所有患者均接受碳酸钙作为口服磷结合剂,以使血清磷水平<6.2 mg/dL。如果出现持续性高钙血症,则将碳酸钙替换为氢氧化铝,直至血钙正常。所有患者每天接受0.25微克骨化三醇治疗。监测的参数包括血清总钙和离子钙、血清磷、磷结合剂摄入量、高钙血症发生率、血清铝、完整甲状旁腺激素(1,84PTH)、骨钙素、碱性磷酸酶、骨密度和手部骨骼X线检查。主要终点为:(a)高钙血症发作次数;(b)含钙磷结合剂的耐受剂量;(c)1,84PTH。治疗6个月后,LCa组患者的总钙和离子钙水平较低(总钙:9.6对10.08 mEq/L,P = 0.005;离子钙:4.76对5.15 mg/dL,P = 0.013)。在LCa组中,记录到的高钙血症发作次数明显较少(血清总钙>10.8 mg/dL:LCa组24次发作,SCa组86次发作;P<0.005)。使用LCa允许给予更多的碳酸钙(平均每日片剂数量:LCa组5.9片,SCa组4.2片;P<0.05)。(摘要截断于250字)

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