Gallieni M, Cozzolino M, Carpani P, Zoni U, Brancaccio D
Renal Unit, San Paolo Hospital, Milan, Italy.
J Nephrol. 2001 May-Jun;14(3):176-83.
Sevelamer HCl, a non-aluminum, non-calcium containing hydrogel, has proved an effective phosphate binder in North American hemodialysis patients. This single-center, open-label, dose titration study assessed the efficacy of sevelamer in a cohort of European hemodialysis patients with different dietary habits, in particular with lower phosphate intake. The aim of the study was to obtain a calcium x phosphate product lower than 60 mg2/dL2 in all patients.
Administration of calcium- or aluminum-based phosphate binders was discontinued during a two-week washout period. Nineteen patients whose serum phosphate level at the end of washout was greater than 5.5 mg/dL (1.78 mmol/L) qualified to receive sevelamer for six weeks. Based on the degree of hyperphosphatemia during washout, patients were started on 403 mg sevelamer capsules with a dose schedule different from previous studies. Only one capsule was administered at breakfast, and the rest of the phosphate binder was divided equally at the two main meals. Sevelamer could be increased by two capsules per day every two weeks, if necessary. A second two-week washout period followed.
Mean serum phosphorus rose from a baseline of 5.3 +/- 1.0 to 7.4 +/- 1.4 mg/dL at the end of washout, then declined to 5.4 +/- 0.8 mg/dL (p < 0.001) by the end of the six-week treatment period and rebounded significantly to 7.1 +/- 1.1 mg/dL after the second two-week washout. Calcium x phosphate product showed a similar pattern, decreasing significantly from 64.1 +/- 14.1 to 46.9 +/- 7.4 mg2/dL2 (p < 0.001) after six weeks of sevelamer. A level of less than 50 mg2/dL2 was reached by 68% of patients, and 95% had less than 60 mg2/dL2. The mean dose of sevelamer at the end of treatment was 3.1 +/- 0.6 g per day. As expected, calcium declined from 9.2 +/- 0.5 to 8.7 mg/dL (p < 0.01) during the initial washout after stopping calcium-based phosphate binders, but remained stable thereafter. Ionized calcium did not change significantly throughout the washout and sevelamer treatment. However, interruption of calcium salts led to a 81% reduction of total calcium intake.
We confirmed in an European sample of hemodialysis patients that sevelamer can reduce phosphate levels without inducing hypercalcemia. The drug can also be successfully used to reduce mean calcium x phosphate levels below 50 mg2/dL2, closer to normal values. Although similar results can be obtained with other phosphate binders, a concomitant accumulation of aluminum, calcium or magnesium could be detrimental to patients.
盐酸司维拉姆是一种不含铝、钙的水凝胶,已被证明是北美血液透析患者有效的磷结合剂。这项单中心、开放标签、剂量滴定研究评估了司维拉姆在一群饮食习惯不同、尤其是磷摄入量较低的欧洲血液透析患者中的疗效。该研究的目的是使所有患者的钙磷乘积低于60mg²/dL²。
在为期两周的洗脱期内停止使用钙基或铝基磷结合剂。19名在洗脱期末血清磷水平高于5.5mg/dL(1.78mmol/L)的患者符合接受司维拉姆治疗六周的条件。根据洗脱期高磷血症的程度,患者开始服用403mg司维拉姆胶囊,剂量方案与以往研究不同。早餐时仅服用一粒胶囊,其余的磷结合剂在两顿主餐时平均分配。如有必要,司维拉姆剂量可每两周增加两粒胶囊。随后是第二个为期两周的洗脱期。
洗脱期末平均血清磷从基线的5.3±1.0mg/dL升至7.4±1.4mg/dL,然后在六周治疗期末降至5.4±0.8mg/dL(p<0.001),在第二个两周洗脱期后显著反弹至7.1±1.1mg/dL。钙磷乘积呈现类似模式,服用司维拉姆六周后从64.1±14.1mg²/dL²显著降至46.9±7.4mg²/dL²(p<0.001)。68%的患者达到低于50mg²/dL²的水平,95%的患者低于60mg²/dL²。治疗期末司维拉姆的平均剂量为每天3.1±0.6g。正如预期的那样,停用钙基磷结合剂后的初始洗脱期内,钙从9.2±0.5mg/dL降至8.7mg/dL(p<0.01),但此后保持稳定。在整个洗脱期和司维拉姆治疗过程中,离子钙没有显著变化。然而,钙盐的中断导致总钙摄入量减少了81%。
我们在欧洲血液透析患者样本中证实,司维拉姆可降低磷水平而不诱发高钙血症。该药物还可成功用于将平均钙磷水平降至50mg²/dL²以下,更接近正常值。尽管使用其他磷结合剂也可获得类似结果,但铝、钙或镁的同时蓄积可能对患者有害。