Diabetes mellitus (DM) is a well-recognized complication of immunosuppressi
ve therapy in the post-transplant (Tx) period. The DM encountered in the se
tting of tacrolimus therapy has been managed in the past by tacrolimus dose
reduction and a rapid corticosteroid taper; frequently insulin therapy is
also required to maintain normoglycemia. However, the dose reduction of imm
unosuppressive agents has often resulted in acute allograft rejection. We a
re reporting our experience in managing three pediatric renal Tx recipients
who developed DM in the post-Tx period while on triple immunosuppressive t
herapy including tacrolimus and corticosteroids. All of our patients were m
anaged by substitution of tacrolimus with conventional doses of neoral whil
e maintaining their usual corticosteroid dose. All three patients had resol
ution of hyperglycemia and none experienced acute rejection. Tacrolimus was
then successfully reinitiated 4.6 months later; at last follow-up, all of
our patients have good allograft function and have maintained a normal bloo
d sugar. In conclusion, we feel that conversion of patients from tacrolimus
to neoral should be attempted as a safer alternative to tacrolimus dose re
duction, for managing post-Tx DM in tacrolimus treated patients.