Division of Nephrology, University of Wisconsin, Madison, WI, USA.
Int J Nanomedicine. 2013;8:3297-307. doi: 10.2147/IJN.S44944. Epub 2013 Aug 26.
Anemia in chronic kidney disease is a prevalent and expensive problem in the United States, and it is well documented that anemia worsens as glomerular filtration rates decline. The complications of severe anemia in this patient population contribute significantly to their overall morbidity with increased cardiovascular complications, decreased quality of life, and increased dependence on transfusions to maintain adequate hemoglobin levels. Erythropoietin-stimulating agents (ESAs) have revolutionized the treatment of anemia in this population, but there has been a great deal of controversy surrounding the quest for the ideal hemoglobin target. In addition, there are economic and practice management implications where anemia treatment is concerned, with ongoing refinement of Centers for Medicare and Medicaid Services-bundled payments. One of the newest additions to the arsenal used to fight anemia in end-stage renal disease patients is peginesatide (Omontys), a synthetic, PEGylated, peptide-based ESA that acts by stimulating the erythropoietin receptor. The role of peginesatide in the future treatment of anemia in chronic kidney disease remains uncertain, with new safety concerns being brought to attention as it emerges on the market, prompting a national recall.
美国慢性肾脏病患者中贫血普遍且昂贵,已有大量文献记录表明贫血会随着肾小球滤过率的下降而恶化。该患者人群重度贫血的并发症会显著增加其整体发病率,包括心血管并发症增加、生活质量下降以及需要更多输血来维持血红蛋白水平。促红细胞生成素刺激剂(ESAs)的出现彻底改变了该人群贫血的治疗方法,但在寻找理想血红蛋白目标方面一直存在很大争议。此外,在贫血治疗方面还存在经济和实践管理方面的影响,医疗保险和医疗补助服务中心的捆绑支付也在不断完善。治疗终末期肾病患者贫血的最新武器之一是培高利特(Omontys),这是一种合成的、聚乙二醇化的、基于肽的 ESA,通过刺激促红细胞生成素受体发挥作用。培高利特在慢性肾脏病贫血治疗中的未来作用仍不确定,随着它在市场上的出现,新的安全问题引起了人们的关注,导致了全国范围内的召回。