首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Hemoglobin stability in patients with anemia, CKD, and type 2 diabetes: An analysis of the TREAT (trial to reduce cardiovascular events with aranesp therapy) placebo arm
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Hemoglobin stability in patients with anemia, CKD, and type 2 diabetes: An analysis of the TREAT (trial to reduce cardiovascular events with aranesp therapy) placebo arm

机译:贫血,CKD和2型糖尿病患者的血红蛋白稳定性:TREAT(尝试通过阿兰斯普疗法减少心血管事件)安慰剂治疗组的分析

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Background: Sparse data are available about the natural history of hemoglobin (Hb) level trends in contemporary patients with anemia, chronic kidney disease (CKD), and type 2 diabetes mellitus. We intended to describe Hb level trends over time with no or minimal administration of erythropoiesis- stimulating agents. Study Design: Prospective clinical trial cohort. Setting & Participants: 2,019 individuals with type 2 diabetes, moderate anemia, and CKD from the placebo arm of the Trial to Reduce Cardiovascular Events With Aranesp Therapy (TREAT) followed up for 2.3 years with an average of 32 monthly Hb level determinations per patient. Darbepoetin alfa was administered only if Hb level decreased to <9 g/dL. Outcomes & Measurements: Number of protocol-directed doses of darbepoetin alfa received due to an Hb level decrease to <9 g/dL. Results: 1,106 (55%) placebo patients consistently maintained an Hb level ??9 g/dL and received no protocol-directed darbepoetin alfa. The other patients received 1 (16%), 2-4 (16%), or 5 or more (13%) doses of darbepoetin alfa. Those who received no darbepoetin alfa doses had higher baseline Hb levels, higher estimated glomerular filtration rates (eGFRs), less proteinuria, and lower ferritin and transferrin saturation values. On average, Hb levels were stable or increased in all groups. Compared with individuals who received no darbepoetin alfa, those who received 5 or more doses were more likely to receive intravenous iron therapy and blood transfusions and progress to renal replacement therapy, but were not at higher risk of death. The strongest predictors of requiring 5 or more doses of darbepoetin alfa were lower baseline Hb level, lower eGFR, and higher proteinuria level. Limitations: Post hoc analysis of a clinical trial of a specific population with diabetes, anemia, and non-dialysis-dependent CKD. Conclusions: In the TREAT placebo arm, Hb levels were stable with no or minimal protocol-directed darbepoetin alfa during 2.3 years of follow-up. Most patients with moderate anemia, non-dialysis- dependent CKD, and type 2 diabetes are able to maintain a stable Hb level without implementing long-term erythropoiesis-stimulating agent therapy. ? 2013 National Kidney Foundation, Inc.
机译:背景:关于贫血,慢性肾脏病(CKD)和2型糖尿病的当代患者血红蛋白(Hb)水平趋势自然史的稀疏数据可用。我们打算描述在不使用或仅使用促红细胞生成促进剂的情况下随时间推移的血红蛋白水平趋势。研究设计:前瞻性临床试验队列。研究与参与者:2,019名患有2型糖尿病,中度贫血和CKD的患者通过Aranesp疗法(TREAT)的安慰剂试验减少了心血管事件,随访了2.3年,每位患者平均每月测定32次Hb。仅当血红蛋白水平降至<9 g / dL时才施用达比泊汀α。结果与测量:由于Hb水平降至<9 g / dL,收到的协议指定剂量的达比泊汀α剂量。结果:1,106名(55%)安慰剂患者始终保持Hb水平≥9 g / dL,且未接受任何针对方案的达比泊汀阿尔法治疗。其他患者接受1(16%),2-4(16%)或5或更多(13%)剂量的darbepoetin alfa。那些未服用达贝泊汀α剂量的患者基线Hb水平较高,估计的肾小球滤过率(eGFR)较高,蛋白尿较少,铁蛋白和转铁蛋白饱和度值较低。平均而言,所有组中的Hb水平均稳定或升高。与未接受darbepoetin alfa的个体相比,接受5次或更多剂量的个体更有可能接受静脉铁疗法和输血并发展为肾脏替代疗法,但死亡风险不高。需要5或更多剂量的darbepoetin alfa的最强预测因素是较低的基线Hb水平,较低的eGFR和较高的蛋白尿水平。局限性:对特定人群患有糖尿病,贫血和非透析依赖性CKD的临床试验进行事后分析。结论:在TREAT安慰剂组中,在2.3年的随访中,无或仅有协议指导的darbepoetin alfa血红蛋白水平稳定。大多数患有中度贫血,非透析依赖型CKD和2型糖尿病的患者能够维持稳定的Hb水平,而无需实施长期的促红细胞生成剂治疗。 ? 2013国家肾脏基金会

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