Optimization of Immunosuppression by Switching From Azathioprine to Enteric-Coated Mycophenolate Sodium in Stable Kidney Transplant Patients
Transplantation Proceedings(2009)
Abstract
The aim of our retrospective, observational, single center study was to analyze renal function changes among stable kidney transplant patients treated with a calcineurin inhibitor (CNI) + azathioprine (AZA), in whom immunosuppression was optimized by a switch from AZA to enteric-coated mycophenolate sodium (EC-MPS) with a view to protecting long-term renal function. Between April 2005 and June 2008, 36 renal transplant patients on previous treatment with a CNI and AZA for a period of 86.94 ± 66.9 months were switched to EC-MPS. After the change, there were no cases of acute rejection episodes. Six patients (16.6%) developed gastrointestinal secondary effects and 5 had to discontinue EC-MPS treatment: 4 due to severe diarrhea 1 due to thrombocytopenia. Among the remaining patients, it was possible to gradually increase the EC-MPS dose (starting at 376 ± 122 mg/d vs current at 533.5 ± 210 mg/d; P < .002), maintaining through levels at 2.1 ± 1.9 ng/mL. Although 11 patients (30.5%) displayed chronic allograft nephropathy upon the preconversion biopsy, at a follow-up of 29.2 ± 9.4 months they showed significantly improved renal function (Modification of Diet in Renal Disease [MDRD4] at change 49.5 ± 19.8 mL/min/1.73 m2 vs current MDRD4 55.6 ± 23.4 mL/min/1.73 m2; P = .02), with no increase in proteinuria (proteinuria at change 0.4 ± 0.4 g/d vs current proteinuria 0.4 ± 0.5 g/d; P = NS). This improvement was evident without changes in CNI levels: cyclosporine at change 133.1 ± 30.2 ng/mL vs current 122 ± 28 ng/mL (P = NS) and tacrolimus at change 7.7 ± 2.2 ng/mL vs current 8.2 ± 2.4 ng/mL (P = NS). In conclusion, conversion from AZA to EC-MPA to optimize immunosuppression seemed to be safe, with no complications in 85% of cases, as well as effective, achieving improved long-term renal function protection. These results suggested a greater protective immunological effect by switching from AZA to EC-MPA.
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Key words
stable kidney transplant patients,immunosuppression,transplant patients,enteric-coated
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