TY - JOUR
T1 - Calcineurin inhibitors and Clostridium difficile infection in adult lung transplant recipients
T2 - The effect of cyclosporine versus tacrolimus
AU - Lee, Janet T.
AU - Whitson, Bryan A.
AU - Kelly, Rosemary F.
AU - D'Cunha, Jonathan
AU - Dunitz, Jordan M.
AU - Hertz, Marshall I.
AU - Shumway, Sara J.
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2013
Y1 - 2013
N2 - Background: Tacrolimus (FK506) has a superior immunosuppressive effect compared with cyclosporine (CSA) without a significant increase in generalized infectious complications. Differences in specific infections such as Clostridium difficile (CDI) have not been reported. We investigated the relationship between calcineurin inhibitors and CDI, hypothesizing that choice of calcineurin inhibitor (CSA or FK506) after lung transplantation would have no effect on the incidence of CDI. Methods: We performed a retrospective chart review of lung transplant recipients between June 1, 2000, and December 31, 2005, at a single institution. Positive CDI assays through December 11, 2011, were also recorded. We used Student's t- and chi-squared tests (α = 0.05) to compare CSA and FK506 groups. We calculated adjusted hazard ratios for CDI using Cox proportional hazard models. Results: We identified 217 lung transplant recipients: 106 patients in the CSA group and 111 patients in the FK506 group. A total of 31 patients (27.9%) in the FK506 group developed CDI postoperatively compared with 20 patients (18.9%) in the CSA group (P = 0.16). The adjusted hazard ratio for CDI in the FK506 group was not significantly higher (1.53; 95% confidence interval, 0.78-2.98).Therewasnosignificant differenceintheintensive care unit or total length of stay, in-hospital incidence rate, timeto firstCDI episode, or recurrence rate between groups. Conclusions: The CDI rates were not significantly higher in the FK506 group than the CSA group in our study. These data are consistent with previous studies on FK506 that show no increase in infectious complications over CSA, and demonstrate its continued safety in lung transplantation.
AB - Background: Tacrolimus (FK506) has a superior immunosuppressive effect compared with cyclosporine (CSA) without a significant increase in generalized infectious complications. Differences in specific infections such as Clostridium difficile (CDI) have not been reported. We investigated the relationship between calcineurin inhibitors and CDI, hypothesizing that choice of calcineurin inhibitor (CSA or FK506) after lung transplantation would have no effect on the incidence of CDI. Methods: We performed a retrospective chart review of lung transplant recipients between June 1, 2000, and December 31, 2005, at a single institution. Positive CDI assays through December 11, 2011, were also recorded. We used Student's t- and chi-squared tests (α = 0.05) to compare CSA and FK506 groups. We calculated adjusted hazard ratios for CDI using Cox proportional hazard models. Results: We identified 217 lung transplant recipients: 106 patients in the CSA group and 111 patients in the FK506 group. A total of 31 patients (27.9%) in the FK506 group developed CDI postoperatively compared with 20 patients (18.9%) in the CSA group (P = 0.16). The adjusted hazard ratio for CDI in the FK506 group was not significantly higher (1.53; 95% confidence interval, 0.78-2.98).Therewasnosignificant differenceintheintensive care unit or total length of stay, in-hospital incidence rate, timeto firstCDI episode, or recurrence rate between groups. Conclusions: The CDI rates were not significantly higher in the FK506 group than the CSA group in our study. These data are consistent with previous studies on FK506 that show no increase in infectious complications over CSA, and demonstrate its continued safety in lung transplantation.
KW - Calcineurin inhibitors
KW - Clostridium difficile
KW - Cyclosporine
KW - Immunosuppression
KW - Lung transplantation
KW - Tacrolimus
KW - Transplant infections
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U2 - 10.1016/j.jss.2013.03.041
DO - 10.1016/j.jss.2013.03.041
M3 - Article
C2 - 23566442
AN - SCOPUS:84884671478
SN - 0022-4804
VL - 184
SP - 599
EP - 604
JO - Journal of Surgical Research
JF - Journal of Surgical Research
IS - 1
ER -