Abstract

PurposeMaintaining target hemoglobin (Hb) with minimal variability is a challenge in hemodialysis (HD) patients. The aim of this study is to compare the long- and short-acting erythropoietin-stimulating agents such as Aranesp and Eprex in achieving these targets.MethodsRandomized, prospective, open-labeled study of 24 weeks includes stable patients on HD >3 months, age >18 years, and on Eprex for >3 months. Patients were randomized into two groups: A-(Aranesp group):HD patients on Eprex Q TIW or BIW were converted to Aranesp Q weekly, by using the conversion factor of 200:1 and those on Eprex Q weekly to Aranesp Q 2 weeks; B-(Eprex group):patients continued on Eprex treatment. Hemoglobin target was set at (105–125 g/l). Primary end points were percentage of patients achieving target Hb, hemoglobin variability, and number of dose changes in each group.ResultsThis study consisted of 139 HD patients: 72 in the Aranesp and 67 in the Eprex—mean (SD) age 54 (16.2) years, 77 (55 %) males. About 46 % were diabetic. Target Hb achieved in 64.8 % of the Aranesp and 59.7 % in the Eprex (p = 0.006). Hb variability was less frequent in the Aranesp group (p = 0.2). Mean number of dose changes was 1.3 (0.87) in the Aranesp and 1.9 (1.2) in the Eprex (p < 0.001). There was 1 vascular access thrombosis in the Aranesp and 8 in the Eprex (p < 0.001). There was no difference in hospitalization and death number between the 2 groups.ConclusionsAranesp Q weekly or every 2 weeks is more efficient in achieving target Hb, with less dose changes and minor vascular access complications.

Highlights

  • The hormone erythropoietin is produced in the kidneys and stimulates the bone marrow production of red blood cells

  • Aranesp Q weekly or every 2 weeks is more efficient in achieving target Hb, with less dose changes and minor vascular access complications

  • The aim of the current study is to compare in hemodialysis patients, between the long-acting Erythropoiesis-stimulating agents (ESAs) (Aranesp) and the shortacting ESA (Eprex), in achieving target Hb and stability, number of dose adjustment, converting factor, outcome, and the cost

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Summary

Introduction

The hormone erythropoietin is produced in the kidneys and stimulates the bone marrow production of red blood cells. Diseased kidneys do not release sufficient amounts of erythropoietin hormone; anemia can result and it is universal in end-stage renal disease (ESRD). Anemia secondary to chronic kidney disease (CKD) is associated with increased hospitalization and decreased survival [1, 2], increased burden of cardiovascular disease [3, 4], and reduced quality of life [5, 6]. With the growing prevalence of CKD [7, 8], new approaches are required to improve the efficiency of anemia management without increasing the workload of health care staff. Erythropoiesis-stimulating agents (ESAs) have been available for almost two decades and remain the central strategy for the treatment for anemia in patients with CKD. The use of ESAs in the management of renal anemia has been shown to improve survival, reduce cardiovascular

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