Adjuvant therapy may allow patients being treated with epoetin to derive gr
eater clinical benefits. Iron supplementation is currently the most widely
used form of adjuvant therapy; intravenous (i.v.) iron is required by the m
ajority of haemodialysis patients receiving epoetin. Measurement of hypochr
omic red blood cells is the most direct way of assessing iron supply to the
bone marrow. During the correction phase, a dose of i.v. iron equivalent t
o 50 mg/day if recommended, with the total dose not exceeding 3 g. When sub
clinical vitamin C deficiency is suspected. ascorbic acid may be given oral
ly (1-1.5 g/week) or i.v. (300 mg three times weekly at the end of dialysis
). The active vitamin D metabolites alfacalcidol and calcitriol may, under
some circumstances, improve anaemia and reduce epoetin dosage requirements.
Vitamin B-6 requirements are increased during epoetin therapy, and supplem
entation at a dose of 100-150 mg/week is recommended. Supplementation of vi
tamin B-12 is optional. Folic acid is supplemented routinely in haemodialys
is patients, though evidence that it increases the efficacy of epoetin is l
imited. Low doses (2-3 mg/week) should normally be sufficient to maintain o
ptimal folic acid stores in epoetin-treated patients, although higher doses
are necessary for patients with hyperhomocysteinaemia. L-Carnitine supplem
entation may be appropriate in some patients with anaemia of chronic renal
failure (CRF) unresponsive to, or requiring large doses of, epoetin. Androg
ens potentially could reduce epoetin costs in countries with limited resour
ces, but should only be used in men older than 50 years with a remnant kidn
ey. Recent animal studies indicate that the combination of epoetin and insu
lin-like growth factor 1 might be beneficial in CRF patients. High doses of
angiotensin-converting enzyme (ACE) inhibitors should be reserved for dial
ysis patients who have hypertension that cannot be controlled by other agen
ts, or who require an ACE inhibitor for treatment of heart failure.