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首页> 外文期刊>BMC Nephrology >Conversion to lanthanum carbonate monotherapy effectively controls serum phosphorus with a reduced tablet burden: a multicenter open-label study
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Conversion to lanthanum carbonate monotherapy effectively controls serum phosphorus with a reduced tablet burden: a multicenter open-label study

机译:多中心开放标签研究表明,转用碳酸镧单一疗法可有效控制血清磷,降低片剂负担

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Background Lanthanum carbonate (FOSRENOL?) is an effective, well-tolerated phosphate binder. The ability of lanthanum to reduce serum phosphorus levels to ≤5.5 mg/dL in patients with end-stage renal disease (ESRD) was assessed in a clinical practice setting. Methods A 16-week, phase IV study enrolled 2763 patients at 223 US sites to evaluate the efficacy of lanthanum carbonate in controlling serum phosphorus in patients with ESRD, and patient and physician satisfaction with, and preference for, lanthanum carbonate after conversion from other phosphate-binder medications. Patients received lanthanum carbonate prescriptions from physicians. These prescriptions were filled at local pharmacies rather than obtaining medication at the clinical trial site. Changes from serum phosphorus baseline values were analyzed using paired t tests. Patient and physician preferences for lanthanum carbonate versus previous medications were assessed using binomial proportion tests. Satisfaction was analyzed using the McNemar test. Daily dose, tablet burden, and laboratory values including albumin-adjusted serum calcium, calcium × phosphorus product, and parathyroid hormone levels were secondary endpoints. Results Serum phosphorus control (≤5.5 mg/dL) was effectively maintained in patients converting to lanthanum carbonate monotherapy; 41.6% of patients had controlled serum phosphate levels at 16 weeks. Patients and physicians expressed markedly higher satisfaction with lanthanum carbonate, and preferred lanthanum carbonate over previous medication. There were significant reductions in daily dose and daily tablet burden after conversion to lanthanum carbonate. Conclusions Serum phosphorus levels were effectively maintained in patients converted from other phosphate-binder medications to lanthanum carbonate, with increased satisfaction and reduced tablet burden. ClinicalTrials.gov: NCT0016012
机译:背景技术碳酸镧(FOSRENOL ?)是一种有效的,耐受性良好的磷酸盐粘合剂。在临床实践中评估了镧将终末期肾病(ESRD)患者的血清磷水平降低至≤5.5mg / dL的能力。方法一项为期16周的IV期研究招募了美国223个地区的2763名患者,以评估碳酸镧在控制ESRD患者中控制血磷的功效以及患者和医生对碳酸镧从其他磷酸盐转化后的满意程度和偏好-粘合剂药物。患者从医师那里收到了碳酸镧处方。这些处方是在当地药房填写的,而不是在临床试验现场获得药物的。使用配对t检验分析血清磷基线值的变化。使用二项式比例测试评估了患者和医师对碳酸镧与先前药物的偏爱。使用McNemar检验分析满意度。次要终点是每日剂量,片剂负担以及包括白蛋白调整后的血清钙,钙×磷产物和甲状旁腺激素水平在内的实验室值。结果转为碳酸镧单药治疗的患者可有效维持血磷控制(≤5.5mg / dL)。 41.6%的患者16周时血清磷酸盐水平得到控制。患者和医师对碳酸镧的满意度明显高于以往,并且首选碳酸镧。转换为碳酸镧后,每日剂量和每日片剂负担显着减少。结论从其他磷酸盐粘合剂药物转换为碳酸镧的患者可有效维持血清磷水平,从而增加满意度并减轻片剂负担。 ClinicalTrials.gov:NCT0016012

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