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Invasive fungal infections in renal transplant patients: a single center study

Background: Timely diagnosis of invasive fungal infections (IFI) in renal transplant (RT) patients on immunosuppression is often difficult, jeopardizing their life and graft. We reported IFI and their causative fungal agents in post-RT patients. Materials and methods: This was a retrospective 6-year...

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Autores principales: Patel, Minaxi H., Patel, Rashmi D., Vanikar, Aruna V., Kanodia, Kamal V., Suthar, Kamlesh S., Nigam, Lovelesh K., Patel, Himanshu V., Patel, Ansy H., Kute, Vivek B., Trivedi, Hargovind L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014505/
https://www.ncbi.nlm.nih.gov/pubmed/28085530
http://dx.doi.org/10.1080/0886022X.2016.1268537
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author Patel, Minaxi H.
Patel, Rashmi D.
Vanikar, Aruna V.
Kanodia, Kamal V.
Suthar, Kamlesh S.
Nigam, Lovelesh K.
Patel, Himanshu V.
Patel, Ansy H.
Kute, Vivek B.
Trivedi, Hargovind L.
author_facet Patel, Minaxi H.
Patel, Rashmi D.
Vanikar, Aruna V.
Kanodia, Kamal V.
Suthar, Kamlesh S.
Nigam, Lovelesh K.
Patel, Himanshu V.
Patel, Ansy H.
Kute, Vivek B.
Trivedi, Hargovind L.
author_sort Patel, Minaxi H.
collection PubMed
description Background: Timely diagnosis of invasive fungal infections (IFI) in renal transplant (RT) patients on immunosuppression is often difficult, jeopardizing their life and graft. We reported IFI and their causative fungal agents in post-RT patients. Materials and methods: This was a retrospective 6-year clinical study carried out from 2010 to 2015 on 1900 RT patients. Clinical data included patient-donor demographics, time to onset of infection, risk factors and graft function in terms of serum creatinine (SCr). To identify IFI, we examined bronchoalveolar lavage (BAL), blood, tissue, and wound swab samples by conventional mycological methods. Results: IFI were diagnosed in 30 (1.56%) patients on triple immunosuppression, mainly males (n = 25) with mean age of 36.57 ± 11.9 years at 13.12 ± 18.35 months post-RT. Aspergillus species was identified in 11 BAL, one tissue, and one wound specimen each, 30.76% of these were fatal and 15.38% caused graft loss; Candida albicans was in nine BAL, four blood, two wound swab, and one tissue specimens, 25% of these were fatal and 25% had graft loss and one mucor in BAL which was fatal. Seven patients were diabetic, 10 had superadded cytomegalovirus infection, and 15 were anti-rejected. Conclusion: IFI are associated with increased morbidity and mortality in RT patients. Triple immunosuppression, broad spectrum antibiotics for ≥ two weeks, diabetes and superadded infection are added risks for these patients. Prevention, early diagnosis, and appropriate management are necessary to improve their prognosis.
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spelling pubmed-60145052018-06-28 Invasive fungal infections in renal transplant patients: a single center study Patel, Minaxi H. Patel, Rashmi D. Vanikar, Aruna V. Kanodia, Kamal V. Suthar, Kamlesh S. Nigam, Lovelesh K. Patel, Himanshu V. Patel, Ansy H. Kute, Vivek B. Trivedi, Hargovind L. Ren Fail Clinical Study Background: Timely diagnosis of invasive fungal infections (IFI) in renal transplant (RT) patients on immunosuppression is often difficult, jeopardizing their life and graft. We reported IFI and their causative fungal agents in post-RT patients. Materials and methods: This was a retrospective 6-year clinical study carried out from 2010 to 2015 on 1900 RT patients. Clinical data included patient-donor demographics, time to onset of infection, risk factors and graft function in terms of serum creatinine (SCr). To identify IFI, we examined bronchoalveolar lavage (BAL), blood, tissue, and wound swab samples by conventional mycological methods. Results: IFI were diagnosed in 30 (1.56%) patients on triple immunosuppression, mainly males (n = 25) with mean age of 36.57 ± 11.9 years at 13.12 ± 18.35 months post-RT. Aspergillus species was identified in 11 BAL, one tissue, and one wound specimen each, 30.76% of these were fatal and 15.38% caused graft loss; Candida albicans was in nine BAL, four blood, two wound swab, and one tissue specimens, 25% of these were fatal and 25% had graft loss and one mucor in BAL which was fatal. Seven patients were diabetic, 10 had superadded cytomegalovirus infection, and 15 were anti-rejected. Conclusion: IFI are associated with increased morbidity and mortality in RT patients. Triple immunosuppression, broad spectrum antibiotics for ≥ two weeks, diabetes and superadded infection are added risks for these patients. Prevention, early diagnosis, and appropriate management are necessary to improve their prognosis. Taylor & Francis 2017-01-13 /pmc/articles/PMC6014505/ /pubmed/28085530 http://dx.doi.org/10.1080/0886022X.2016.1268537 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Patel, Minaxi H.
Patel, Rashmi D.
Vanikar, Aruna V.
Kanodia, Kamal V.
Suthar, Kamlesh S.
Nigam, Lovelesh K.
Patel, Himanshu V.
Patel, Ansy H.
Kute, Vivek B.
Trivedi, Hargovind L.
Invasive fungal infections in renal transplant patients: a single center study
title Invasive fungal infections in renal transplant patients: a single center study
title_full Invasive fungal infections in renal transplant patients: a single center study
title_fullStr Invasive fungal infections in renal transplant patients: a single center study
title_full_unstemmed Invasive fungal infections in renal transplant patients: a single center study
title_short Invasive fungal infections in renal transplant patients: a single center study
title_sort invasive fungal infections in renal transplant patients: a single center study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014505/
https://www.ncbi.nlm.nih.gov/pubmed/28085530
http://dx.doi.org/10.1080/0886022X.2016.1268537
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