4.2 Article

Immunosuppressive therapy and infection after kidney transplantation

Journal

TRANSPLANT INFECTIOUS DISEASE
Volume 12, Issue 5, Pages 397-405

Publisher

WILEY
DOI: 10.1111/j.1399-3062.2010.00526.x

Keywords

sirolimus; cytomegalovirus; transplantation; immunosuppressive therapy; infection; kidney transplant

Funding

  1. Ministerio de Sanidad y Consumo, Instituto de Salud Carlos III-FEDER [RESITRA G03/075]
  2. Spanish Network for the Study of Infection in Transplantation (RESITRA) [G03/075]
  3. Spanish Study Group of Infection in Transplantation of the Spanish Society of Infectious Diseases and Clinical Microbiology (GESITRA-SEIMC)

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P>Background The role of immunosuppressive drugs in the development of infection in transplant recipients has been poorly analyzed. Objective To evaluate the possible association between infection and immunosuppression regimens in a large cohort of renal transplant recipients. Methods All renal transplant recipients included in the RESITRA prospective cohort from August 2003 to February 2005 with a minimum follow-up of 3 months were studied. An intention-to-treat analysis was performed and patients were analyzed in groups according to the type of induction and initial maintenance therapy. Viral, bacterial, and fungal infections occurring during this period were evaluated. Results A total of 1398 renal transplant recipients were studied. A maintenance regimen containing sirolimus was independently associated with a lower risk of cytomegalovirus (CMV) infection (odds ratio [OR], 0.16; 95% confidence interval [CI], 0.05-0.54) and with a higher rate of surgical site infection (OR, 3.21; 95% CI, 1.26-8.21). Excluding treatment used for acute rejection episodes, no other factors related to the immunosuppression regimens were associated with the development of bacteremia, urinary infections, pneumonia, or other infections. Conclusion The use of sirolimus as maintenance therapy in kidney recipients is associated with a low rate of CMV infection and with a higher risk of surgical site infection.

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