2009
DOI: 10.1159/000253958
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Low-Molecular-Weight Iron Dextran in the Management of Renal Anaemia in Patients on Haemodialysis – the IDIRA Study

Abstract: Background: Intravenous iron supplementation is a basic principle in the therapy of haemodialysis (HD) patients with renal anaemia. In the Iron Dextran in Renal Anaemia (IDIRA) study, we analysed the efficacy of a therapy with low-molecular-weight iron dextran (LMW-ID) in stable HD patients with adequate iron stores previously treated with ferric gluconate. Methods: IDIRA was an open-label, prospective, non-randomized, observational multicenter trial over 12 months in iron-repleted HD patients. All patients we… Show more

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Cited by 3 publications
(2 citation statements)
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“…1) [7,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58], representing 24 single-arm or cohort studies and 10 parallel-arm RCT; 32 studies (94%) were published in full-text articles and 2 (6%) were scientific abstracts. The characteristics of the individual studies are displayed in table 1.…”
Section: Resultsmentioning
confidence: 99%
“…1) [7,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58], representing 24 single-arm or cohort studies and 10 parallel-arm RCT; 32 studies (94%) were published in full-text articles and 2 (6%) were scientific abstracts. The characteristics of the individual studies are displayed in table 1.…”
Section: Resultsmentioning
confidence: 99%
“…The efficacy and safety of IV ferumoxytol was comparable to IV iron sucrose in patients with varying degrees of renal function [ 205 ]. Intravenous low-molecular-weight iron dextran for 12 months was effective even in iron-pretreated HD patients [ 206 ]. Furthermore, ferric pyrophosphate citrate, a water-soluble iron salt administered via dialysate at a dose of 2 μmol/L (110 mg/L of Fe 3+ ) to supply ∼5–7 mg of iron during the course of each dialysis session, was able to decrease the amount of IV iron needed for maintenance of tHb with a reduction of the ESA dose in HD patients [ 207 ].…”
Section: Safety Issues Of Iron Therapymentioning
confidence: 99%