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Pediatric renal transplantation with mycophenolate mofetil-based immunosuppression without induction: results after three years
Authors:Jungraithmayr Therese,Staskewitz Astrid,Kirste Günter,Böswald Michael,Bulla Monika,Burghard Rainer,Dippell Jürgen,Greiner Christel,Helmchen Udo,Klare Bernd,Klaus Günter,Leichter Heinz E,Mihatsch Michael J,Michalk Dietrich V,Misselwitz Joachim,Plank Christian,Querfeld Uwe,Weber Lutz T,Wiesel Manfred,Tönshoff Burkhard,Zimmerhackl Lothar B  German Pediatric Renal Transplantation Study Group
Affiliation:Zentrum für Kinderheilkunde und Jugendmedizin, Freiburg, Germany.
Abstract:BACKGROUND: Mycophenolate mofetil (MMF)-based immunosuppression has reduced the acute rejection rate in adults and in children in the early posttransplantation period. Three-year posttransplantation results have been reported for adults but not for children thus far. In the present open-labeled study, patients 18 years old and younger were evaluated prospectively for up to 3 years after renal transplantation (RTX). METHODS: Eighty-six patients receiving MMF in combination with cyclosporine and prednisone without induction were evaluated for patient survival, transplant survival, renal function, arterial blood pressure, adverse events, and opportunistic infections. These patients were compared with a historic control group (n=54) receiving azathioprine (AZA) instead of MMF. RESULTS: Patient survival after 3 years was 98.8% in the MMF group and 94.4% in the AZA group (NS). Intent-to-treat analysis of graft survival demonstrated superiority for MMF (98% vs. 80%; P<0.001). Cumulative acute rejection episodes occurred in 47% of patients in the MMF group versus 61% in the AZA group (P<0.05). Renal function was not significantly different, neither after 3 years nor in the long-term calculation. Antihypertensive medication was administered to 73% to 84% of patients, similar in both groups. Opportunistic infections were recorded only for MMF. Infection rates were comparable to those reported in adults. CONCLUSIONS: These results suggest that MMF is safe and beneficial as a longer term maintenance immunosuppressive drug in children and adolescents.
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