Objective: Iron supplementation plays a major role in erythropoietin-treate
d end-stage renal disease patients. For peritoneal dialysis (PD) patients,
oral iron substitution is more convenient than intravenous therapy, However
, disturbed iron absorption and adverse effects may be limiting factors for
oral treatment. Nevertheless, we compared the response to a high-dose and
low-dose oral iron absorption test between PD patients and healthy control
subjects.
Patients and Interventions: In 34 PD patients and 15 healthy control subjec
ts, blood samples were taken at baseline as well as 2, 4, and 8 hours after
oral intake of 4 tablets iron sulfate (105 mg elemental iron per tablet).
In a subgroup of 6 PD patients and 6 control subjects, the oral iron absorp
tion test was repeated using 1 tablet iron sulfate.
Results: There was no significant difference in the increase in serum iron
during the test between the two groups. As known for healthy subjects, iron
absorption was significantly better in PD patients with absolute iron defi
ciency compared to those with functional iron deficiency. Iron-repleted PD
patients showed the lowest iron absorption, indicating that a high dose of
oral iron did not overwhelm the ability of the bowel tract to reject unneed
ed iron. Increasing the oral iron dose from 1 to 4 tablets was followed by
a better response in a small subgroup of PD patients compared to control su
bjects. Side effects such as nausea and vomiting occurred more frequently d
uring high-dose oral iron in control subjects than in PD patients (20% vs 8
.8%).
Conclusion: High-dose oral iron is well absorbed in iron-depleted PD patien
ts. This kind of oral iron therapy should be considered in some subgroups o
f PD patients with iron deficiency, particularly in those patients with poo
r vascularization of arm veins or intolerance to intravenous iron preparati
ons.