Related Experiment Video
Updated: Mar 29, 2026

Digital Home-Monitoring of Patients after Kidney Transplantation: The MACCS Platform
Published on: April 12, 2021
Mycophenolate mofetil versus enteric-coated mycophenolate sodium after simultaneous pancreas-kidney transplantation
E B Rangel1, C S Melaragno, J R Sá
1Nephrology Division, Universidade Federal de São Paulo, Rua Botucatu, 740 VilaClementino, 04023-900 São Paulo, Brazil. erikabr@uol.com.br
Introduction:
Adverse gastrointestinal events are frequent after mycophenolate use. The objectives of the present study were to report the incidence of acute noninfectious diarrhea, to determine the risk factors, and to compare the severity of reactions between mycophenolate mofetil (MMF) and enteric-coated mycophenolate sodium (EC-MPS) after simultaneous pancreas kidney transplantation (SPKT).
Methods:
We included 165 SPKT patients from December 2000 to May 2007. Uni- and multivariate analyses were performed, using acute noninfectious diarrhea as the dependent variable. P < .05 was considered significant.
Results:
Mean age and duration of dialysis and of diabetes were 34.9 +/- 8.2 years, 27.3 +/- 18.3 months, and 21.9 +/- 16.2 years, respectively. Sixty-three percent used MMF, 36.4% used EC-MPS, and 0.6% used azathioprine. Multivariate analysis showed that the duration of diabetes (P = .049, confidence interval [CI] 1.0- 1.13) and MMF use (P = .013, 95% CI 0.2-0.82) were the main determinants of acute diarrhea after SPKT. MMF dose reduction (79.2% vs 62.3%, P = .024) and severity of diarrhea associated with orthostatic hypotension were more pronounced among MMF than EC-MPS patients (42.4% vs 15.1%, P = .001). There was no difference between MMF and EC-MPS after dose reduction in relation to the occurrence of acute kidney rejection (30.8% vs 26.7%, P = .53).
Conclusions:
Acute noninfectious diarrhea after SPKT was related to the duration of diabetes and to prescription of MMF. Preferential use of EC-MPS was associated with a lower necessity of dose reduction and less severe episodes of acute diarrhea compared with MMF, although dose reduction was equally associated with acute episodes of kidney rejection.
Insights
Acute noninfectious diarrhea after pancreas kidney transplantation is linked to diabetes duration and mycophenolate mofetil (MMF) use. Enteric-coated mycophenolate sodium (EC-MPS) showed fewer severe diarrhea episodes and less MMF dose reduction.
Area of Science:
- Nephrology
- Transplantation Immunology
- Gastroenterology
Background:
- Gastrointestinal adverse events are common following mycophenolate immunosuppression.
- Understanding risk factors for diarrhea is crucial in post-transplant care.
Purpose of the Study:
- To determine the incidence of acute noninfectious diarrhea post-simultaneous pancreas kidney transplantation (SPKT).
- To identify risk factors associated with this adverse event.
- To compare the severity and management of diarrhea between mycophenolate mofetil (MMF) and enteric-coated mycophenolate sodium (EC-MPS).
Main Methods:
- A cohort of 165 SPKT patients was analyzed.
- Univariate and multivariate regression analyses were employed to identify determinants of acute diarrhea.
- Statistical significance was set at P < .05.
Main Results:
- Longer diabetes duration and MMF use were significant risk factors for acute diarrhea (P = .049 and P = .013, respectively).
- MMF use was associated with a higher incidence of dose reduction (79.2% vs 62.3%) and more severe diarrhea with orthostatic hypotension (42.4% vs 15.1%) compared to EC-MPS.
- No significant difference in acute kidney rejection rates was observed between MMF and EC-MPS groups after dose reduction (30.8% vs 26.7%).
Conclusions:
- Acute noninfectious diarrhea following SPKT is associated with diabetes duration and MMF therapy.
- EC-MPS demonstrates a favorable profile with reduced diarrhea severity and lower dose reduction rates compared to MMF.
- While EC-MPS may mitigate gastrointestinal side effects, careful monitoring for kidney rejection post-dose reduction remains essential for both formulations.
Related Concept Videos
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions
Extracorporeal Removal of Drugs: Continuous Renal Replacement Therapy
Kidney Transplant I: Introduction
Kidney Transplant III: Nursing Management
Kidney Transplant II: Surgical Procedure

