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Experience of the use of enteric coated sodium mycophenolate in renal transplant patients

Abstract

Aim of the study was to investigate the efficacy, safety and tolerability of sodium mycophenolate after renal transplantation. Material: 183 renal transplant recipients from 16 centers were analysed. The 1st (de novo) group of 83 recipients who received sodium mycophenolate since renal transplantation (RT) in combination with prednisolone and cyclosporine. The 2nd (maintenance) group of 100 patients was switched from mophetyl mycophenolate or azathioprine to myfortic after 57,3 ± 48,6 months after RT. The duration of follow-up was 6 months. The efficacy of immunosuppression was evaluated by the rates of acute rejection, graft survival, serum creatinine level (Pcr) and creatinine clearance. For the analysis of safety and tolerability of sodium mycophenolate sodium, the frequency of adverse effects and dose reduction/drug withdrawal were taken into account. Results: In de novo group acute rejection was detected in 6% of patients. The 6-month patients and grafts survival were 98,7% and 98,7%, respectively. Pcr at 3 and 6 months of observation was 120 ± 32 mM and 124 ± 38 mM, respectively. Infections haved developed in 44,5%, hepatic disorders in 13%, leucopenia in 12% and gastrointestinal complications in 7,2% of patients. The sodium mycophenolate dose was reduced in 7 (8,4%) patients due to development of adverse effects. No acute rejection was observed in maintenance group. Patient and graft survival at 6 months were 100% and 98%, respectively. Two grafts were lost due to chronic rejection. Pcr at 3 and 6 months of observation was 137 ± 43 mM and 134 ± 47 mM, respectively. Infections in this group occurred in 27%, liver dysfunction in 6%, gastrointestinal disorders in 10% and leucopenia in 11% of patients. In 13 (13%) of patients mycophenolate sodium dose was reduced, and in 3 of those the drug was cancelled completely thereafter. Conclusions : Preliminary results of the study confirmed data of other authors about high efficacy and safety of in basic immunosuppressive therapy after renal transplantation. The adverse effects of sodium mycophenolate can restrict its application to a limited number of patients.

About the Authors

I. G. Kim
ФНЦ Трансплантологии и искусственных органов им. В.И. Шумакова, г. Москва
Russian Federation


E. S. Stolyarevich
ФНЦ Трансплантологии и искусственных органов им. В.И. Шумакова, г. Москва
Russian Federation


R. N. Vedernikova
ФНЦ Трансплантологии и искусственных органов им. В.И. Шумакова, г. Москва
Russian Federation


N. A. Tomilina
ФНЦ Трансплантологии и искусственных органов им. В.И. Шумакова, г. Москва
Russian Federation


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Review

For citations:


Kim I.G., Stolyarevich E.S., Vedernikova R.N., Tomilina N.A. Experience of the use of enteric coated sodium mycophenolate in renal transplant patients. Nephrology and Dialysis. 2010;12(2):106-110. (In Russ.)

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