Deflazacort (DFZ) pharmacokinetics was evaluated in fifteen pediatric
patients on chronic hemodialysis or after renal transplantation, and i
n three normal children. After overnight fasting: oral DFZ 0.26 +/- 0.
01 mg/kg (mean +/- SEM) was given. Serial blood samples were collected
for 360 min and analyzed by HPLC for 21-hydroxy-DFZ (21-HO-DFZ). Seru
m concentration profiles and pharmacokinetic parameters were similar i
n patients on hemodialysis, renal transplant recipients and normal chi
ldren. Elimination half-life was longer in the 9 cyclosporine-treated
subjects (108.0 +/- 13.6 min) than in the other nine (71.2 +/- 8.3 min
; p < 0.02). Our finding suggests that, from a pharmacokinetic point o
f view DFZ dose adjustment for renal function is not necessary in chil
dren with chronic renal failure or after renal transplantation.