COST-MINIMIZATION ANALYSIS OF USING SHORT AND LONG-ACTING ERYTHROPOESIS-STIMULATING AGENTS FOR CORRECTION OF NEPHROGENIC ANEMIA AGAINST THE BACKGROUND OF SUBSTITUTION THERAPY

I. Krysanov, E. Y. Ermakova, L. Vaskova, M. Tiapkina
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引用次数: 2

Abstract

Clinical trials conducted in various countries indicate that the use of epoetin alfa in patients with nephrogenic anemia in chronic kidney disease can increase the effectiveness of treatment, reduce the incidence of cardiovascular and infectious complications, and reduce mortality in patients with chronic kidney disease.The aim of the article was to conduct a comparative clinical and economic assessment of the treatment costs of nephrogenic anemia in adult dialysis patients with recombinant human erythropoietins: epoetin alfa, darbepoetin and long-acting methoxy polyethylene glycol – epoetin beta.Materials and methods. The study took into account direct medical costs of nephrogenic anemia pharmacotherapy on the basis of 1 year maintenance therapy according to the following scheme: epoetin alfa – 3 times per week, darbepoetin alfa – once per week, methoxy polyethylene glycol – epoetin beta – once per 2 or 4 weeks. A “costs minimization” analysis was performed for equivalent maintenance epoetins doses for intravenous and subcutaneous administrations. Epoetin alpha equivalents were calculated for an average patient weighing 75 kg by converting a weekly dose of short-acting epoetin (7500 IU) into equivalent doses using dose conversion factors.Results. In the hypothetical cohort of patients under study, epoetin alfa, darbepoetin alfa, and methoxy polyethylene glycol – epoetin beta not differ in effectiveness in achieving target Hb values and in safety. With the equal effectiveness of the investigated drugs, in the studied patients, intravenous epoetin alfa can be less expensive drug therapy relative to the equivalent doses obtained by the calculation: darbepoetin by 14–24% and methoxy polyethylene glycol – epoetin beta by 4–30%. The change-over of patients to the subcutaneous administration makes it possible to decline a weekly dose of epoetin alfa by 20–30% by reducing the frequency of taking the drug to twice a week, and to reduce the cost of drug therapy by a third.Conclusion. Intravenous and subcutaneous administrations of epoetin alfa 2500 IU may be a more economical drug therapy in comparison with the equivalent doses of darbepoetin and methoxy polyethylene glycol – epoetin beta.
在替代疗法的背景下,使用短效和长效促红细胞生成剂矫正肾源性贫血的成本最小化分析
各国进行的临床试验表明,在慢性肾病肾源性贫血患者中使用促生成素可提高治疗效果,减少心血管和感染性并发症的发生率,降低慢性肾病患者的死亡率。本文的目的是对成人透析患者肾源性贫血的治疗成本进行比较临床和经济评估重组人促红细胞生成素:促红细胞生成素α、达贝泊丁和长效甲氧基聚乙二醇-促红细胞生成素β。材料和方法。该研究在1年维持治疗的基础上考虑了肾源性贫血药物治疗的直接医疗费用,根据以下方案:每周一次促生成素- 3次,每周一次达贝泊丁-每周一次,甲氧基聚乙二醇-促生成素-每2或4周一次。对静脉和皮下给药的同等维持剂量进行了“成本最小化”分析。通过使用剂量转换因子将每周短效Epoetin (7500 IU)的剂量转换为等效剂量,计算平均体重75 kg的患者的Epoetin α当量。在假设的研究患者队列中,epoetin α、darbepoetin α和甲氧基聚乙二醇- epoetin β在达到目标Hb值的有效性和安全性方面没有差异。在所研究药物的有效性相同的情况下,在所研究的患者中,相对于计算得出的等效剂量:达贝泊丁为14-24%,甲氧基聚乙二醇- β为4-30%,静脉注射肾上腺素可以更便宜的药物治疗。患者改为皮下给药,通过将服用频率减少到每周两次,可以使每周一次的促生成素剂量减少20-30%,并使药物治疗费用减少三分之一。与同等剂量的达贝泊丁和甲氧基聚乙二醇-促生成素相比,静脉注射和皮下注射2500 IU促生成素可能是一种更经济的药物治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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