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Elsevier, Kidney International, 4(73), p. 511-512, 2008

DOI: 10.1038/sj.ki.5002756

Elsevier, Kidney International, 5(72), p. 638-642, 2007

DOI: 10.1038/sj.ki.5002422

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Iron sucrose causes greater proteinuria than ferric gluconate in non-dialysis chronic kidney disease

Journal article published in 2007 by R. Agarwal ORCID, Ar R. Rizkala, Mo O. Kaskas, R. Minasian, J. R. Trout, B. L. Jaber
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Non-dextran intravenous (i.v.) iron preparations seem to differentially affect proteinuria in patients with chronic kidney disease. To study effects of ferric gluconate and iron sucrose on proteinuria, we conducted a crossover trial in 12 patients with stage 3-4 chronic kidney disease. These patients were randomized to receive the same dose of either drug 1 week apart. Urine samples were obtained immediately before and at frequent intervals after the drug. The urine total protein/creatinine ratio was significantly greater after iron sucrose than ferric gluconate treatment with the effect noted within 15 min post-infusion. Furthermore, when iron sucrose was given first, a significantly greater protein/creatinine ratio was seen subsequently with ferric gluconate than with the reverse order of treatment. The urine albumin/creatinine ratio was also significantly greater with iron sucrose than with ferric gluconate. There was no significant difference, however, between the two i.v. irons in the measured urine N-acetyl-beta-D-glucosaminidase/creatinine ratio. Although our study showed that acutely, iron sucrose increased proteinuria, the long-term effects of repeated i.v. non-dextran iron on kidney function requires further study.