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Historical clinical and economic consequences of anemia management in patients with end-stage renal disease on dialysis using erythropoietin stimulating agents versus routine blood transfusions: a retrospective cost-effectiveness analysis

机译:使用促红细胞生成素刺激剂与常规输血相比,终末期肾病患者贫血治疗的历史临床和经济后果:回顾性成本 - 效果分析

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摘要

Objective: To determine whether Medicare's decision to cover routine administration of erythropoietin stimulating agents (ESAs) to treat anemia of end-stage renal disease (ESRD) has been a cost-effective policy relative to standard of care at the time. Methods: The authors used summary statistics from the actual cohort of ESRD patients receiving ESAs between 1995 and 2004 to create a simulated patient cohort, which was compared with a comparable simulated cohort assumed to rely solely on blood transfusions. Outcomes modeled from the Medicare perspective included estimated treatment costs, life-years gained, and quality-adjusted life-years (QALYs). Incremental cost-effectiveness ratio (ICER) was calculated relative to the hypothetical reference case of no ESA use in the transfusion cohort. Sensitivity of the results to model assumptions was tested using one-way and probabilistic sensitivity analyses. Results: Estimated total costs incurred by the ESRD population were $155.47B for the cohort receiving ESAs and $155.22B for the cohort receiving routine blood transfusions. Estimated QALYs were 2.56M and 2.29M, respectively, for the two groups. The ICER of ESAs compared to routine blood transfusions was estimated as $873 per QALY gained. The model was sensitive to a number of parameters according to one-way and probabilistic sensitivity analyses. Limitations: This model was counter-factual as the actual comparison group, whose anemia was managed via transfusion and iron supplements, rapidly disappeared following introduction of ESAs. In addition, a large number of model parameters were obtained from observational studies due to the lack of randomized trial evidence in the literature. Conclusions: This study indicates that Medicare's coverage of ESAs appears to have been cost effective based on commonly accepted levels of willingness-to-pay. The ESRD population achieved substantial clinical benefit at a reasonable cost to society.
机译:目的:确定医疗保险是否决定涵盖常规促进促红细胞生成素刺激剂(ESAs)治疗末期肾病(ESRD)的贫血,这是当时的护理标准的成本效益的政策。方法:作者使用来自1995年和2004年之间接受ESAS的实际核心群体的综述统计数据,以创建模拟患者队列,该群体与具有可比模拟的群体进行比较,假设依赖于输血。从Medicare角度建模的结果包括估计的治疗成本,获得的生命年份,以及质量调整的生命年龄(QALYS)。相对于输血队列中没有ESA的假设参考案例计算增量成本效益比(ICER)。使用单向和概率敏感性分析测试结果对模型假设的结果的敏感性。结果:核心核心核算局估计的核心股份人口的总成本为155.47亿美元,接收欧川队员和155.22亿美元用于接受常规输血的队列。两组分别为2.56米和2.29米的估计QALYs分别为2.56亿和2.29米。与常规输血相比的ESAS的转换器估计每次QALY每次QALY为873美元。根据单向和概率敏感性分析,该模型对许多参数敏感。局限性:该模型作为实际比较组的逆事实,其贫血通过输血和铁补充剂进行管理,在引入ESA后迅速消失。此外,由于文献中缺乏随机试验证据,从观察性研究获得了大量模型参数。结论:本研究表明,基于普通接受的愿意支付水平,Medicare对ESA的覆盖率似乎具有成本效益。 ESRD人口以合理的成本实现了大量的临床益处。

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