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Transplant Proc ; 37(2): 895-8, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15848568

ABSTRACT

UNLABELLED: Basiliximab added to a maintenance regimen consisting of cyclosporine microemulsion and mycophenolate mofetil was studied for its effectiveness in allowing early steroid withdrawal in renal transplantation. Furthermore, the cyclosporine-sparing effects between groups with and without basiliximab induction therapy were compared. PATIENTS: Between September 2001 and June 2003, 90 patients underwent renal transplants with cyclosporine-based immunosuppression, namely, cyclosporine, mycophenolate mofetil, and methylprednisolone, (group 1; n = 25). During the latter half of the study basiliximab was administered during the induction phase (group 2; n = 65). In group 2, steroids were completely withdrawn on postoperative day 14 in 57 patients. RESULTS: The incidence of acute rejection was significantly higher among group 1 patients (P = .005). The incidence of steroid-resistant rejection in group 1 patients was significantly higher (P = .025). At each time point cyclosporine levels in group 1 patients were significantly higher (P < .01). The incidence of infection was comparable between the groups. Patient and graft survival rates in group 1 were 100% and 100%; in group 2, they were 99% and 99%, respectively. In group 2, steroids were discontinued in 57 patients with permanent withdrawal achieved in 32 patients (56%). CONCLUSION: The use of basiliximab, together with mycophenolate mofetil allowed for a significant reduction in the cyclosporine dose without increasing the risk of acute rejection. Although further follow-up is necessary to confirm the effect, this regimen may attenuate cyclosporine nephrotoxicity thereby affecting the long-term outcomes of renal transplantation.


Subject(s)
Antibodies, Monoclonal/therapeutic use , Cyclosporine/therapeutic use , Graft Rejection/epidemiology , Kidney Transplantation/immunology , Mycophenolic Acid/analogs & derivatives , Recombinant Fusion Proteins/therapeutic use , Basiliximab , Dose-Response Relationship, Drug , Drug Administration Schedule , Drug Therapy, Combination , Graft Rejection/prevention & control , Humans , Immunosuppressive Agents/therapeutic use , Methylprednisolone/therapeutic use , Mycophenolic Acid/therapeutic use
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