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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
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.
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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
title_full Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
title_fullStr Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
title_full_unstemmed Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
title_short Rifaximin use favoured micafungin-resistant Candida spp. infections in recipients of allogeneic hematopoietic cell transplantation
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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