Skip Navigation


NDT Advance Access originally published online on July 12, 2008
Nephrology Dialysis Transplantation 2008 23(12):4049-4053; doi:10.1093/ndt/gfn387
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
23/12/4049    most recent
gfn387v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Hanvesakul, R.
Right arrow Articles by Cockwell, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hanvesakul, R.
Right arrow Articles by Cockwell, P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org



Increased incidence of infections following the late introduction of mycophenolate mofetil in renal transplant recipients

Rajesh Hanvesakul, Chandrashekhar Kubal, Seema Jham, Esha Sarkar, Kevin Eardley, Dwomoa Adu and Paul Cockwell

Department of Nephrology and Renal Transplantation, University Hospital Birmingham, Edgbaston, Birmingham B15 2TH, UK

Correspondence and offprint requests to: Rajesh Hanvesakul, Department of Nephrology and Renal Transplantation, University Hospital Birmingham, Edgbaston, Birmingham B15 2TH, UK. Tel: +44-7980800867; Fax: +44-7980800867; E-mail: rhanvesakul{at}doctors.org.uk



  Abstract

Background. Late introduction of mycophenolate mofetil (MMF) is used in renal transplant patients to allow calcineurin inhibitor (CNI) withdrawal. This change in treatment may alter the immunosuppressive load predisposing patients to infections. To assess this we have analysed infection rates in 30 consecutive patients with chronic allograft nephropathy commenced on MMF for CNI withdrawal.

Methods and results. The study period was from 12 months pre-commencement to 12 months post-commencement. At commencement, patient mean age was 51.2 ± 12.9 years and mean time post-transplant was 3170 ± 2130 days. Estimated glomerular filtration rate (eGFR) at the start of the study period and at conversion was 30.7 ± 12.1 ml/min and 23.1 ± 9.9 ml/min, respectively. The mean dose of MMF post-conversion was 1575 ± 428 mg/day. Estimated GFR had stabilized at 12 months post-conversion to 25.3 ± 12.2 ml/min. There was a significant increase in infections following conversion: pre-conversion, 26.7% (8/30); post-conversion, 66.6% (20/30) ({chi}2 = 24.5, P < 0.0005). There was an inverse correlation between eGFR at conversion and infection rates post-conversion (r = –0.379, P = 0.039). There were no hospitalizations for infection pre-conversion and 6 patients (20%) were hospitalized post-conversion, for a total of 285 days (7–107).

Conclusion. There is significant morbidity associated with an increased incidence of infection after late introduction of MMF at standard doses in renal transplant recipients. This risk may be related to GFR at the time of conversion.

Keywords: chronic allograft nephropathy (CAN); CNI withdrawal; infections; mycophenolate mofetil (MMF); renal transplant

Received for publication: 7. 1.08
Accepted in revised form: 19. 6.08


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.