Literature DB >> 12544890

Severe acute renal failure after exposure to sirolimus-tacrolimus in two living donor kidney recipients.

Loredo Lawsin1, Jimmy A Light.   

Abstract

BACKGROUND: We began a clinical trial in African Americans comparing sirolimus-tacrolimus to standard immunosuppression. We report two African American male living donor kidney recipients who developed acute renal failure after exposure to sirolimus-tacrolimus.
METHODS: Both patients received similar doses of sirolimus and tacrolimus to achieve target levels of 5 to 15 ng/mL and prednisone in tapering doses. Renal function and tacrolimus and sirolimus levels were systematically monitored.
RESULTS: Although both kidneys functioned immediately, acute oliguric renal failure developed approximately 2 weeks after transplantation. Transplant kidney biopsy showed acute tubular necrosis in patient 2. Sirolimus-tacrolimus was then stopped in both patients. Both patients required temporary hemodialysis. Renal function returned 2 weeks later and was normal 2 months after transplantation on tacrolimus plus mycophenolate mofetil.
CONCLUSION: Combination sirolimus-tacrolimus may cause nephrotoxicity in some patients by mechanisms that are presently unexplained.

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Year:  2003        PMID: 12544890     DOI: 10.1097/00007890-200301150-00029

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  2 in total

Review 1.  Benefit-risk assessment of sirolimus in renal transplantation.

Authors:  Dirk R J Kuypers
Journal:  Drug Saf       Date:  2005       Impact factor: 5.606

Review 2.  Therapeutic approach to FSGS in children.

Authors:  Debbie S Gipson; Keisha Gibson; Patrick E Gipson; Sandra Watkins; Marva Moxey-Mims
Journal:  Pediatr Nephrol       Date:  2006-11-16       Impact factor: 3.714

  2 in total

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