Parker KP, LaCoursiere T, Macon EJ, Stivelman JC, Bailey JL, Mitch WE, Sands JM
Can the erythropoietin dose be lowered safely? A case-control study of subcutaneous administration
Am Soc Nephrol
J Am Soc Nephrol (abstract) (Nov) 6:880 1995

Erythropoietin (epo) is extremely expensive, and accounts for about 25% of the budget for hemodialysis therapy. Thus, any method for reducing the cost of this therapy would be appreciated. This group previously showed that administration of epo subcutaneously once a week, using 1/3 of the weekly iv dose, could maintain a stable hematocrit in 4 dialysis patients for 6 months. They have extended their initial report by preforming a cross-over trial of subcutaneous vs intravenous epo. Patients were initially stabilized on iv epo for 6 months, crossed over to sc epo for 10 months, then returned to iv epo for 5 months. Again, the patients were given a sc dose equal to 1/3 of the weekly iv dose. The amount of iron given did not differ between the two groups. Both treatments were able to maintain stable hemoatocrits, reticulocyte counts, iron saturation, and ferritin. In addition, there was no change in dialysis indices (Kt/V, PCR, albumin, and PTH). The only side-effect was stinging at the injection site, which required discontinuation of sc epo in about 20% of patients. The group is working do develop a more appropriate diluent to minimize this side effect. Thus, weekly subcutaneous epo is safe, effective, and allows for a substantial reduction in the dose and cost of epo therapy.

Additional comments by Steven Fishbane: Several studies have documented an improved erythropoietic response when erythropoietin is administered sub-q vs. iv. Sub-q dosing has not, however, become routinely used in clinical practice, probably because the modest reduction in EPO doses is at the expense of subjecting the patient to frequent injections. In this study, HD patients treated with iv EPO were converted to once weekly sub-q EPO at 1/3rd the original weekly dose. 27 patients completed 10 months of follow-up and were compared to 27 retrospectively matched controls. The main result was that hematocrits were maintained as well in the sub-q as in the iv group, but at 1/3 the weekly EPO dose.

Comment: Despite the nonrandomized design, and a difficulty in iron management during the study period, this is probably the most important anemia study reported at the ASN. Given the high cost of EPO therapy, a 2/3 reduction in dosing would be very significant, and I think that most patients would find once weekly injections to be acceptable. (Star)

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Am Soc Nephrol
CRF by problem area : Anemia/Erythropoietin/Iron