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首页> 外文期刊>Clinical nephrology >Lanthanum carbonate (Fosrenol) efficacy and tolerability in the treatment of hyperphosphatemic patients with end-stage renal disease.
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Lanthanum carbonate (Fosrenol) efficacy and tolerability in the treatment of hyperphosphatemic patients with end-stage renal disease.

机译:碳酸镧(Fosrenol)在高磷血症晚期肾病患者中的疗效和耐受性。

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AIMS: High serum phosphorus levels are a common problem in patients receiving long-term dialysis treatment. Lanthanum carbonate (Fosrenol) is a new non-aluminum, non-calcium phosphate binder developed for the treatment of hyperphosphatemia in patients with end-stage renal disease (ESRD). We report data from a recent trial, which, for the first time, assessed the efficacy and tolerability of lanthanum carbonate treatment, compared with placebo, in Chinese patients with ESRD. PATIENTS AND METHODS: Following a one- to three-week washout phase and a four-week, open-label lanthanum carbonate dose-titration phase, male and female hemodialysis patients were randomized (1:1) to receive either lanthanum carbonate or placebo for four weeks. The primary efficacy parameter of the study was the control of serum phosphorus levels (< or =1.8 mmol/l [< or = 5.6 mg/dl]). Secondary endpoints included the profile of serum phosphorus during titration and parathyroid hormone, calcium, and calcium x phosphorus (Ca x P) product levels. The safety and tolerability of lanthanum carbonate were assessed by monitoring adverse events throughout the study. RESULTS: Mean serum phosphorus level at the end of washout was 2.5 +/- 0.5 mmol/l (7.7 +/- 1.5 mg/dl; n=73), and there was no evidence of a difference in levels between the treatment groups pre-randomization. At the end of the study, lanthanum carbonate-treated patients had significantly lower phosphorus levels (1.6 +/- 0.5 mmol/l [5.1 +/- 1.5 mg/dl]; n=30) than those receiving placebo (2.3 +/- 0.4 mmol/l [7.2 +/- 1.3 mg/dl]; n=31; p < 0.001). In addition, a significantly higher proportion of patients receiving lanthanum carbonate had controlled serum phosphorus levels (60%) compared with the placebo group (10%; p < 0.001). Ca x P product levels were also significantly lower in the lanthanum carbonate group at the end of randomized treatment (p < 0.001). Lanthanum carbonate was well tolerated; only one serious adverse event was reported, which was unrelated to treatment. CONCLUSIONS: Lanthanum carbonate was shown to be an effective and well-tolerated phosphate binder for the treatment of hyperphosphatemia in Chinese patients with ESRD. This finding supports the results of previous US and European studies, which have also shown that lanthanum carbonate treatment effectively controls serum phosphorus levels.
机译:目的:血清磷水平高是接受长期透析治疗的患者的普遍问题。碳酸镧(Fosrenol)是一种新型的非铝,非磷酸钙粘合剂,被开发用于治疗终末期肾病(ESRD)患者的高磷酸盐血症。我们报告了一项最近试验的数据,该试验首次评估了碳酸镧治疗与安慰剂相比在中国ESRD患者中的疗效和耐受性。患者和方法:在1至3周的洗脱期和4周的开放标签碳酸镧剂量滴定阶段之后,将男性和女性血液透析患者随机(1:1)接受碳酸镧或安慰剂治疗四周。该研究的主要功效参数是控制血清磷水平(<或= 1.8 mmol / l [<或= 5.6 mg / dl])。次要终点包括滴定过程中的血清磷水平以及甲状旁腺激素,钙和钙x磷(Ca x P)产物水平。在整个研究过程中,通过监测不良事件来评估碳酸镧的安全性和耐受性。结果:洗脱结束时的平均血清磷水平为2.5 +/- 0.5 mmol / l(7.7 +/- 1.5 mg / dl; n = 73),并且没有证据表明治疗前各治疗组之间的水平存在差异-随机化。在研究结束时,碳酸镧治疗的患者的磷水平(1.6 +/- 0.5 mmol / l [5.1 +/- 1.5 mg / dl]; n = 30)显着低于接受安慰剂的患者(2.3 +/-) 0.4 mmol / l [7.2 +/- 1.3 mg / dl]; n = 31; p <0.001)。此外,与安慰剂组(10%; p <0.001)相比,接受碳酸镧治疗的患者血清磷水平得到控制的比例(60%)明显更高。在随机治疗结束时,碳酸镧组的Ca x P产物水平也显着降低(p <0.001)。碳酸镧具有良好的耐受性。据报道只有一个严重的不良事件,与治疗无关。结论:碳酸镧被证明是一种有效且耐受性良好的磷酸盐结合剂,可用于治疗中国ESRD患者的高磷酸盐血症。这一发现支持了先前美国和欧洲研究的结果,这些研究还表明,碳酸镧处理可有效控制血清磷水平。

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