Intravenous iron dextran treatment in predialysis patients with chronic renal failure

Citation
K. Dahdah et al., Intravenous iron dextran treatment in predialysis patients with chronic renal failure, AM J KIDNEY, 36(4), 2000, pp. 775-782
Citations number
31
Categorie Soggetti
Urology & Nephrology
Journal title
AMERICAN JOURNAL OF KIDNEY DISEASES
ISSN journal
02726386 → ACNP
Volume
36
Issue
4
Year of publication
2000
Pages
775 - 782
Database
ISI
SICI code
0272-6386(200010)36:4<775:IIDTIP>2.0.ZU;2-8
Abstract
Iron deficiency anemia is common in patients with chronic renal failure not undergoing hemodialysis. Current therapy consists of oral or intravenous ( IV) iron dextran (IVID). The standard IV regimen is 100 to 200 mg/dose for a 1-g total dose. We hypothesized that 500 mg/wk of IVID for two doses woul d be less costly and equally effective as 200 mg/wk for five doses. We pros pectively studied 22 patients with creatinine clearances less than 50 mL/mi n who were not undergoing dialysis and had anemia and evidence of iron defi ciency (ferritin level <100 ng/mL or transferrin saturation [TSAT] <20%). P atients were randomized into two groups: group I (n = 8), 200 mg/wk of IVID for 5 weeks, and group II (n = 14), 500 mg/wk of IVID for;! weeks. AII pat ients tolerated IVID infusions without serious adverse reactions. Over the 6-month follow-up, both groups experienced an increase in hemoglobin levels from baseline. Ferritin levels in both groups increased (P < 0.005), peake d at 2 weeks, then declined thereafter. Over the 6-month follow-up, both gr oups experienced significant improvement, although the beneficial effects o f group II declined at a significantly faster rate than group I (P = 0.003) . There was no significant difference in change in ferritin levels between groups. TSAT peaked at 2 weeks in both groups (P < 0.001). Group I experien ced a significant increase in TSAT throughout the 6-month follow-up (P < 0. 03), and group II achieved a significant increase in TSAT at 2 weeks, but n ot at 3 and 6 months. There was no significant difference in pretreatment t o posttreatment change in TSAT. Treatment in group II was 35.2% more cost-e ffective than in group 1 ($965 versus $1,490, respectively). We conclude th at IVID, 500 mg/wk, for 2 weeks is as effective and safe as 200 mg/wk for 5 weeks, but much less costly. (C) 2000 by the National Kidney Foundation, I nc.