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首页> 外文期刊>BMC Nephrology >Lanthanum carbonate versus placebo for management of hyperphosphatemia in patients undergoing peritoneal dialysis: a subgroup analysis of a phase 2 randomized controlled study of dialysis patients
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Lanthanum carbonate versus placebo for management of hyperphosphatemia in patients undergoing peritoneal dialysis: a subgroup analysis of a phase 2 randomized controlled study of dialysis patients

机译:碳酸镧与安慰剂治疗腹膜透析患者的高磷酸盐血症:透析患者2期随机对照研究的亚组分析

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Background This short-term study assessed the efficacy and safety of lanthanum carbonate in the treatment of hyperphosphatemia in dialysis patients; here, we report a prespecified subgroup analysis of patients undergoing peritoneal dialysis. Methods Men and women (n = 39) who had received continuous ambulatory peritoneal dialysis for chronic kidney disease for 6?months or more were enrolled in eight renal medicine departments in the United Kingdom. A 2-week washout period was followed by a 4-week dose-titration phase during which patients received lanthanum carbonate titrated up to 2250?mg/day. This was followed by a 4-week, randomized, placebo-controlled, parallel-group phase during which patients continued to receive either lanthanum carbonate at the titrated dose, or a matched dose of placebo. The main outcome measure was control of serum phosphate levels (1.3-1.8?mmol/l) at the end of the parallel-group phase. Results Serum phosphate was controlled in 3/39 (8%) patients at the beginning of the dose-titration phase (after washout) and in 18/31 (58%) patients treated with lanthanum carbonate at its end. After the parallel-group phase, 60% of lanthanum carbonate-treated patients and 10% of those receiving placebo had controlled serum phosphate. There was no difference in mean (95% confidence interval) serum phosphate levels between groups at randomization: lanthanum carbonate, 1.57 (1.34-1.81) mmol/l; placebo, 1.58 (1.40-1.76) mmol/l (p = 0.96). However, a difference was seen at the end of the parallel-group phase: lanthanum carbonate, 1.56 (1.33-1.79) mmol/l; placebo, 2.25 (1.81-2.68) mmol/l (p = 0.0015). There were no clinically important changes in nutritional parameters and no serious treatment-related adverse events were recorded. Conclusions At doses up to 2250?mg/day, lanthanum carbonate is well tolerated and controls hyperphosphatemia effectively. Treatment with higher doses of lanthanum carbonate may allow patients undergoing peritoneal dialysis the potential to increase their dietary protein intake without compromising their phosphate control.
机译:背景这项短期研究评估了碳酸镧治疗透析患者高磷酸盐血症的疗效和安全性。在这里,我们报告了进行腹膜透析患者的预先指定的亚组分析。方法在英国的八个肾脏内科就诊了连续9个月或更长时间因慢性肾脏病接受非卧床腹膜透析的男女(n = 39)。在为期2周的洗脱期之后,接着是4周的剂量滴定阶段,在此期间,患者接受的碳酸镧滴定至2250?mg / day。随后进行为期4周的随机,安慰剂对照,平行组研究,在此期间,患者继续接受滴定剂量的碳酸镧或安慰剂的匹配剂量。主要结果指标是在平行组阶段结束时控制血清磷酸盐水平(1.3-1.8?mmol / l)。结果在剂量滴定阶段开始(洗脱后)时,控制了3/39(8%)患者的磷酸盐血清,在结束时用碳酸镧治疗的18/31(58%)患者中的磷酸盐血清得到控制。在平行组阶段后,接受碳酸镧治疗的患者中有60%和接受安慰剂的患者中有10%的患者血清磷酸盐控制了。随机分组时,两组之间的平均血清磷酸盐水平没有差异(95%置信区间):碳酸镧1.57(1.34-1.81)mmol / l;安慰剂1.58(1.40-1.76)mmol / l(p = 0.96)。但是,在平行基团阶段结束时发现了差异:碳酸镧1.56(1.33-1.79)mmol / l;碳酸镧1.56(1.33-1.79)mmol / l。安慰剂,2.25(1.81-2.68)mmol / l(p = 0.0015)。营养参数没有临床上重要的变化,也没有记录到与治疗相关的严重不良事件。结论在高达2250mg / day的剂量下,碳酸镧具有良好的耐受性,可有效控制高磷血症。用更高剂量的碳酸镧治疗可以使接受腹膜透析的患者增加饮食中蛋白质的摄入量而又不影响磷酸盐的控制。

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