Abstract

Objective: To study the efficacy of intravenous erythropoietin and subcutaneous erythropoietin in hemodialysis patients who have persistent anemia despite correction of iron therapy and to measure the outcomes in terms of raise in haemoglobin concentration and adverse events in both the groups.Methods: After ethical committee approval the current study was conducted at the Department of Hemodialysis of Owasi Hospital and Research Centre, Hyderabad a period of 6 mo duration. 60 patients undergoing hemodialysis were recruited into out study who had haemoglobin less than 10.0 despite corrected iron levels. Patients were divided into two groups for intravenous administration and subcutaneous administration of alpha erythropoietin. Patients were stratified into three sub-groups of mild, moderate and severe anaemia. Therapeutic response was recorded in the form of monthly hemoglobin and hemoatocrit. Of the 30 patients in the subcutaneous group, erythropoietin was given to 19 males and 11 females, while intravenous erythropoietin was administered to 17 males and 13 females in the other 30 patients.Results: The mean hemoglobin level in the subcutaneous group was 5.16 at the commencement of the study and in the intravenous group the mean hemoglobin was 5.0. In the subcutaneous group, the mean rise in the hemoglobin was rapidly achieved in 3 mo duration when compared to the intravenous group. Mean Systolic Blood pressure was higher in the intravenous group when compared to the subcutaneous group. Spillage of the drug was minimal in subcutaneous group when compared to the intravenous group.Conclusion: After correction of the iron deficiency, low dose of erythropoietin subcutaneously promised to maintain expected hemoglobin level above 10 g/dL with no adverse events compared to intravenous erythropoietin. Erythropoitin alpha at a dose of 4000 IU was enough to achieve the therapeutic target of Hemoglobin>10.0 by administering subcutaneously accelerated hypertension was less when compared to Intravenous erythropieitn post dialysis. Hence we recommend to use erythropoietin subcutaneously rather than intravenously.

Highlights

  • Chronic kidney disease is a global health problem rising across the world due to diabetes and hypertension

  • 60 patients were divided into 2 equal groups receiving subcutaneous erythropoietin and intravenous erythropoietin at a dose of 4000 units per session

  • There was a significant elevation in the mean hemoglobin levels with respect to the fixed dose of 4000 units per session over the subcutaneous and intravenous route which demonstrated that the increase in hemoglobin levels was substantially high in the subcutaneous group over a period of 6 mo duration

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Summary

Introduction

Chronic kidney disease is a global health problem rising across the world due to diabetes and hypertension. End stage renal disease is associated with multiple problems like anemia, volume overload and increased risk of death. The World Health Organization (WHO) defines anemia as hemoglobin (Hgb) concentration below 13.0 g/dl for adult men and below 12.0 g/dl for mature women [2]. Renal anemia is a major complication in patients with chronic kidney disease, dialysis patients. The prevalence of anemia increases from 1% in patients with an eGFR of 60 ml/mil/1.73m2 (stage III CKD) to 9% at an eGFR rate of 30 ml/min/1.73m2 (stage IV CKD) and to 33% for men and 67% for women at an eGFR of 15 ml/min/1.73m2 (Stage V CKD) [3]. Correction of anemia is essential and the target hemoglobin up to 12 g/dl helps in regressing the heart failure [4]

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