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.