Safety and Efficacy of Total Dose Iron Dextran Administration in Patients on Home Renal Replacement Therapies

Author:

Sloand James A.1,Shelly Mark A.1,Erenstone Anne L.1,Schiff Melissa J.1,Talley Thomas E.1,Dhakal Madhavendra P.1

Affiliation:

1. Nephrology and Infectious Disease Divisions, Department of Medicine, Highland Hospital, University of Rochester School of Medicine and Dentistry, Rochester, New York, U.S.A.

Abstract

Objective To determine the safety and efficacy of intravenous total dose iron (TDI) replacement in patients treated with home renal replacement therapy. Design Prospective open-label study on end points in the population studied. Setting Institutional outpatient home dialysis program. Patients The study included 20 end-stage renal disease (ESRD) patients, performing chronic peritoneal or home hemodialysis, with iron deficiency defined as ferritin < 100 ng/mL and/or an iron saturation < 20%. Intervention The total dose of iron dextran was calculated and infused at a rate not exceeding 6 mg/min. Hemoglobin, hematocrit, iron studies, and liver function tests (LFTs) were obtained before and 3 to 4 weeks after TDI infusion. Hematocrit of patients failing to achieve an increase in Hct over this period was re-examined 2 to 4 weeks later looking for a delayed response. Main Outcome Measures Primary end points for efficacy were changes in Hct, ferritin, and iron saturation. Toxicity was measured as reported immediate and delayed symptoms and elevated transaminases and/or alkaline phosphatase levels. Results A median iron dose of 1000 mg (range, 325 1500 mg) was administered. The infusions were generally well tolerated. Clinical adverse effects were seen in 2 patients weighing less than 50 kg. No increase in LFT results was seen. Hematocrit increased 2.2% (95% CI, 0.5% -3.9%) from 29.0% to 31.2% (p = 0.01) within 4 weeks of infusion. Significant increases also occurred in iron saturation (from 13% to 22%, p = 0.001) and ferritin (from 234 to 305 ng/mL, p = 0.008). Among the 9 patients who did not respond with a significant increase in Hct, 2 had a delayed response, increasing the overall response from 63% at 4 weeks to 71 %,8 weeks after TDI.lnadequate erythropoietin dosing and low-grade infectious/inflammatory disorders may have contributed to a poor response in several patients. Conclusion Total dose iron is a safe and effective means of restoring iron and erythropoietic response in ESRD patients weighing more than 50 kg who receive their renal replacement therapy at home.

Publisher

SAGE Publications

Subject

Nephrology,General Medicine

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Iron salts;Meyler's Side Effects of Drugs;2016

2. Blood Conservation Techniques;Journal of Infusion Nursing;2013-09

3. Effect of Intravenous Iron Sucrose in Peritoneal Dialysis Patients Who Receive Erythropoiesis-Stimulating Agents for Anemia: A Randomized, Controlled Trial;Clinical Journal of the American Society of Nephrology;2006-03-29

4. Iron salts;Meyler's Side Effects of Drugs: The International Encyclopedia of Adverse Drug Reactions and Interactions;2006

5. A randomized, controlled trial comparing IV iron sucrose to oral iron in anemic patients with nondialysis-dependent CKD;Kidney International;2005-12

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