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Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
Damage to gut mucosa following conditioning regimens may favour bacterial infections that can trigger graft versus host disease (GvHD) in patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT). Rifaximin, an oral and non-absorbable antibiotic, has been recently proposed as eff...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357665/ https://www.ncbi.nlm.nih.gov/pubmed/34180023 http://dx.doi.org/10.1007/s00277-021-04569-x |
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author | Marzuttini, Francesca Mancusi, Antonella Bonato, Samanta Griselli, Mario Tricarico, Sara Casarola, Genni Paradiso, Matteo Ruggeri, Loredana Terenzi, Adelmo Merluzzi, Mara Prigitano, Anna Tortorano, Anna Maria Pitzurra, Lucia Falini, Brunangelo Carotti, Alessandra Velardi, Andrea Pierini, Antonio |
author_facet | Marzuttini, Francesca Mancusi, Antonella Bonato, Samanta Griselli, Mario Tricarico, Sara Casarola, Genni Paradiso, Matteo Ruggeri, Loredana Terenzi, Adelmo Merluzzi, Mara Prigitano, Anna Tortorano, Anna Maria Pitzurra, Lucia Falini, Brunangelo Carotti, Alessandra Velardi, Andrea Pierini, Antonio |
author_sort | Marzuttini, Francesca |
collection | PubMed |
description | Damage to gut mucosa following conditioning regimens may favour bacterial infections that can trigger graft versus host disease (GvHD) in patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT). Rifaximin, an oral and non-absorbable antibiotic, has been recently proposed as effective prophylaxis to reduce bacterial infections in the gut and consequently acute GvHD in this setting. The present study evaluated safety and outcomes of HSCT patients that were treated with rifaximin prophylaxis at Perugia University Hospital. Rifaximin prophylaxis was introduced as standard of care in HSCT patients in May 2018. We retrieved data from 118 consecutive transplants, and we compared the outcomes of rifaximin-treated patients with historical controls that did not receive antibiotic prophylaxis. While incidences of neutropenic fever, documented bacterial infections, and aGvHD were similar in the two groups, we found an increased frequency of invasive candidiasis and clinically relevant Candida spp. infections in rifaximin-treated patients (5 patients vs 1 patient, 25% [± 0.99%] vs 1% [± 0.01%], p < .0001). Three rifaximin-treated patients experienced life-threating candidemia (2 C. krusei, 1 C. orthopsilosis). Rifaximin was the only factor that increased the risk of Candida spp. infections. Rifaximin could have contributed to microbiome disruption which favoured an outbreak of life-threatening Candida infections. This important complication forced us to halt its use. Larger, prospective studies are needed to assess the impact of rifaximin prophylaxis on incidence of bacterial infections, aGvHD, and survival of HSCT patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-021-04569-x. |
format | Online Article Text |
id | pubmed-8357665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-83576652021-08-30 Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation Marzuttini, Francesca Mancusi, Antonella Bonato, Samanta Griselli, Mario Tricarico, Sara Casarola, Genni Paradiso, Matteo Ruggeri, Loredana Terenzi, Adelmo Merluzzi, Mara Prigitano, Anna Tortorano, Anna Maria Pitzurra, Lucia Falini, Brunangelo Carotti, Alessandra Velardi, Andrea Pierini, Antonio Ann Hematol Original Article Damage to gut mucosa following conditioning regimens may favour bacterial infections that can trigger graft versus host disease (GvHD) in patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT). Rifaximin, an oral and non-absorbable antibiotic, has been recently proposed as effective prophylaxis to reduce bacterial infections in the gut and consequently acute GvHD in this setting. The present study evaluated safety and outcomes of HSCT patients that were treated with rifaximin prophylaxis at Perugia University Hospital. Rifaximin prophylaxis was introduced as standard of care in HSCT patients in May 2018. We retrieved data from 118 consecutive transplants, and we compared the outcomes of rifaximin-treated patients with historical controls that did not receive antibiotic prophylaxis. While incidences of neutropenic fever, documented bacterial infections, and aGvHD were similar in the two groups, we found an increased frequency of invasive candidiasis and clinically relevant Candida spp. infections in rifaximin-treated patients (5 patients vs 1 patient, 25% [± 0.99%] vs 1% [± 0.01%], p < .0001). Three rifaximin-treated patients experienced life-threating candidemia (2 C. krusei, 1 C. orthopsilosis). Rifaximin was the only factor that increased the risk of Candida spp. infections. Rifaximin could have contributed to microbiome disruption which favoured an outbreak of life-threatening Candida infections. This important complication forced us to halt its use. Larger, prospective studies are needed to assess the impact of rifaximin prophylaxis on incidence of bacterial infections, aGvHD, and survival of HSCT patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-021-04569-x. Springer Berlin Heidelberg 2021-06-28 2021 /pmc/articles/PMC8357665/ /pubmed/34180023 http://dx.doi.org/10.1007/s00277-021-04569-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Marzuttini, Francesca Mancusi, Antonella Bonato, Samanta Griselli, Mario Tricarico, Sara Casarola, Genni Paradiso, Matteo Ruggeri, Loredana Terenzi, Adelmo Merluzzi, Mara Prigitano, Anna Tortorano, Anna Maria Pitzurra, Lucia Falini, Brunangelo Carotti, Alessandra Velardi, Andrea Pierini, Antonio Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation |
title | Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
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title_full | Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
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title_fullStr | Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
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title_full_unstemmed | Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
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title_short | Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
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title_sort | rifaximin use favoured micafungin-resistant candida spp. infections in recipients of allogeneic hematopoietic cell transplantation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357665/ https://www.ncbi.nlm.nih.gov/pubmed/34180023 http://dx.doi.org/10.1007/s00277-021-04569-x |
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