Rwg. Gruessner et al., SUGGESTED GUIDELINES FOR THE USE OF TACROLIMUS IN PANCREAS KIDNEY TRANSPLANTATION/, Clinical transplantation, 12(3), 1998, pp. 260-262
As experience with tacrolimus (FK506, Prograf(R)) accumulates and redu
ced rejection rates are increasingly demonstrated, some transplant cen
ters are adopting tacrolimus-based primary immunosuppressive regimens
for their patients undergoing pancreas/kidney transplantation. The gui
delines provided in this article based on the experience of four major
US transplant centers, cover issues related to dosing, blood levels,
concomitant use of mycophenolate mofetil (MMF), antifungal and antivir
al prophylaxis, and drug interactions, For post-transplant immunosuppr
ession some centers initiate oral tacrolimus administration on postope
rative day 1, 2, or 3, while others wait until day 6 or 7, when renal
or gastrointestinal function has resumed. Most centers endeavor to ach
ieve higher target trough levels (similar to 10-20 ngl/mL, but not hig
her) in the first 3 months post-transplant, reducing levels thereafter
. Several centers are now using MMF instead of azathioprine as an adju
nct to tacrolimus. Conversion from cyclosporine to tacrolimus during m
aintenance therapy is often considered in the event of rejection or wh
en adverse events do not respond to dosage reduction.