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Acute Injury with Intravenous Iron and Concerns Regarding
Acute Injury with Intravenous Iron and Concerns Regarding
Long-Term Safety
Kalkidan Bishu and Rajiv Agarwal
Division of Nephrology, Department of Medicine, Indiana University School of Medicine, and Richard L. Roudebush
VA Medical Center, Indianapolis, Indiana
Intravenous iron is widely used to maintain adequate iron stores and prevent iron deficiency anemia in patients with chronic
kidney disease, yet concerns remain about its long-term safety with respect to oxidative stress, kidney injury, and accelerated
atherosclerosis, which are the subjects of this review. Three parenteral iron formulations are available for use in the United
States: Iron dextran, iron gluconate, and iron sucrose. Iron dextran, especially the high molecular form, has been linked with
anaphylactoid and anaphylactic reactions, and its use has been declining. A portion of intravenous iron preparations is
redox-active, labile iron available for direct donation to transferrin. In vitro tests show that commonly available intravenous
iron formulations have differing capacities to saturate transferrin directly: Iron gluconate iron sucrose iron dextran.
Intravenous iron treatment produces oxidative stress, as demonstrated by increases in plasma levels of lipid peroxidation
products (malondialdehyde), at a point that is much earlier than the time to peak concentration of catalytically active iron,
suggesting a direct effect of iron sucrose on oxidative stress. Furthermore, iron sucrose infusion produces endothelial
dysfunction that seems to peak earlier than the serum level of free iron. Intravenous iron sucrose infusion also has been shown
to produce acute renal injury and inflammation as demonstrated by increased urinary albumin, enzyme (N-acetyl--
glucosaminidase), and cytokine (chemokine monocyte chemoattractant protein-1) excretions. Although the long-term dangers
of intravenous iron are unproved, these data call for examination of effects of intravenous iron on the potential for long-term
harm
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