TY - JOUR
T1 - Randomized cross-over comparison of intravenous and subcutaneous darbepoetin dosing efficiency in haemodialysis patients
AU - Cervelli, Matthew J.
AU - Gray, Nicholas
AU - McDonald, Stephen
AU - Gentgall, Melanie G.
AU - Disney, Alex P S
PY - 2005/4
Y1 - 2005/4
N2 - Background: Studies have consistently shown the superior dosing efficiency of subcutaneous (s.c.) compared to intravenous (i.v.) erythropoietin (r-HuEPO). Unlike r-HuEPO, data from pivotal darbepoetin trials support s.c. and i.v. dosing equivalence, however, no blinded cross-over randomized studies of s.c. and i.v. dose efficiency or intra-patient variability in response have been published. Methods: During this 12-month study, 53 haemodialysis patients were randomized to s.c. or i.v. darbepoetin for a 6-month period and then switched to the alternative route for a second 6-month period. Darbepoetin dose was titrated during the first 4-months of each period to acheive a stable haemoglobin during the final 2-month observation period of each arm. Results: Twenty-four patients were included in analysis. No significant difference between s.c. and i.v. administration was observed for any measured parameter. Patients acheived a non-significantly higher haemoglobin (123.6 ± 3.76 vs 120.9 ± 4.42 g/L, P = 0.11) from a non-significantly lower darbepoetin dose (40.8 ± 10.7 vs 42.5 ± 11.0 meg/week, P = 0.23) with i.v. administration. The population-based weight normalized s.c./i.v. dose ratio was 1.04 (0.97-1.11). Despite no significant overall difference, some patients experienced changes in individual dose efficiency response. Three of 24 patients recorded a greater than 30% change, four of 24 recorded between a 20 and 30% change, and five of 24 patients recorded between a 10 and 20% change relative to i.v. dose efficiency. Conclusions: This study further supports s.c. and i.v. dosing equality and that overall the more convenient i.v. route can be used with equal dosing efficiency. However, patients switching routes of administration should be monitored due to the wide range in individual response.
AB - Background: Studies have consistently shown the superior dosing efficiency of subcutaneous (s.c.) compared to intravenous (i.v.) erythropoietin (r-HuEPO). Unlike r-HuEPO, data from pivotal darbepoetin trials support s.c. and i.v. dosing equivalence, however, no blinded cross-over randomized studies of s.c. and i.v. dose efficiency or intra-patient variability in response have been published. Methods: During this 12-month study, 53 haemodialysis patients were randomized to s.c. or i.v. darbepoetin for a 6-month period and then switched to the alternative route for a second 6-month period. Darbepoetin dose was titrated during the first 4-months of each period to acheive a stable haemoglobin during the final 2-month observation period of each arm. Results: Twenty-four patients were included in analysis. No significant difference between s.c. and i.v. administration was observed for any measured parameter. Patients acheived a non-significantly higher haemoglobin (123.6 ± 3.76 vs 120.9 ± 4.42 g/L, P = 0.11) from a non-significantly lower darbepoetin dose (40.8 ± 10.7 vs 42.5 ± 11.0 meg/week, P = 0.23) with i.v. administration. The population-based weight normalized s.c./i.v. dose ratio was 1.04 (0.97-1.11). Despite no significant overall difference, some patients experienced changes in individual dose efficiency response. Three of 24 patients recorded a greater than 30% change, four of 24 recorded between a 20 and 30% change, and five of 24 patients recorded between a 10 and 20% change relative to i.v. dose efficiency. Conclusions: This study further supports s.c. and i.v. dosing equality and that overall the more convenient i.v. route can be used with equal dosing efficiency. However, patients switching routes of administration should be monitored due to the wide range in individual response.
KW - Darbepoetin
KW - Dose
KW - Efficiency
KW - Intravenous
KW - Subcutaneous
UR - http://www.scopus.com/inward/record.url?scp=20144376223&partnerID=8YFLogxK
U2 - 10.1111/j.1440-1797.2005.00386.x
DO - 10.1111/j.1440-1797.2005.00386.x
M3 - Article
C2 - 15877671
AN - SCOPUS:20144376223
SN - 1320-5358
VL - 10
SP - 129
EP - 135
JO - Nephrology
JF - Nephrology
IS - 2
ER -