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Breakthrough invasive fungal diseases during voriconazole treatment for aspergillosis: A 5-year retrospective cohort study
Breakthrough invasive fungal diseases (bIFDs) during voriconazole treatment are concerning, as they are associated with high rates of mortality and pathogen distribution. To evaluate the prevalence, incidence, patient characteristics, including IFD events, and overall mortality of bIFDs during voric...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654366/ https://www.ncbi.nlm.nih.gov/pubmed/27562861 http://dx.doi.org/10.1093/mmy/myw067 |
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author | Kim, Sun Bean Cho, Sung-Yeon Lee, Dong-Gun Choi, Jae-Ki Lee, Hyo-Jin Kim, Si-Hyun Park, Sun Hee Choi, Su-Mi Choi, Jung-Hyun Yoo, Jin-Hong Lee, Jong-Wook |
author_facet | Kim, Sun Bean Cho, Sung-Yeon Lee, Dong-Gun Choi, Jae-Ki Lee, Hyo-Jin Kim, Si-Hyun Park, Sun Hee Choi, Su-Mi Choi, Jung-Hyun Yoo, Jin-Hong Lee, Jong-Wook |
author_sort | Kim, Sun Bean |
collection | PubMed |
description | Breakthrough invasive fungal diseases (bIFDs) during voriconazole treatment are concerning, as they are associated with high rates of mortality and pathogen distribution. To evaluate the prevalence, incidence, patient characteristics, including IFD events, and overall mortality of bIFDs during voriconazole treatment for invasive aspergillosis (IA). We retrospectively analyzed the medical records of consecutive patients who had undergone voriconazole treatment for IA and who had bIFD events between January 2011 and December 2015. Eleven bIFD events occurred in 9 patients. The prevalence and incidence of bIFDs were 2.25% (9/368) and 0.22 cases per year, respectively. Overall mortality was 44.4% (4/9). The severity of the illness and persistence of immunodeficiency, mixed infection, and low concentration of the treatment drug at the site of infection were identified as possible causes of bIFDs. Seven of 11 events (63.6%) required continued voriconazole treatment with drug level monitoring. In 4 (36.3%) cases, the treatment was changed to liposomal amphotericin B. Two cases resulted in surgical resection (18.2%). Clinicians should be aware that bIFDs during voriconazole treatment for IA can occur, and active therapeutic approaches are required in these cases. |
format | Online Article Text |
id | pubmed-5654366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56543662017-10-30 Breakthrough invasive fungal diseases during voriconazole treatment for aspergillosis: A 5-year retrospective cohort study Kim, Sun Bean Cho, Sung-Yeon Lee, Dong-Gun Choi, Jae-Ki Lee, Hyo-Jin Kim, Si-Hyun Park, Sun Hee Choi, Su-Mi Choi, Jung-Hyun Yoo, Jin-Hong Lee, Jong-Wook Med Mycol Original Article Breakthrough invasive fungal diseases (bIFDs) during voriconazole treatment are concerning, as they are associated with high rates of mortality and pathogen distribution. To evaluate the prevalence, incidence, patient characteristics, including IFD events, and overall mortality of bIFDs during voriconazole treatment for invasive aspergillosis (IA). We retrospectively analyzed the medical records of consecutive patients who had undergone voriconazole treatment for IA and who had bIFD events between January 2011 and December 2015. Eleven bIFD events occurred in 9 patients. The prevalence and incidence of bIFDs were 2.25% (9/368) and 0.22 cases per year, respectively. Overall mortality was 44.4% (4/9). The severity of the illness and persistence of immunodeficiency, mixed infection, and low concentration of the treatment drug at the site of infection were identified as possible causes of bIFDs. Seven of 11 events (63.6%) required continued voriconazole treatment with drug level monitoring. In 4 (36.3%) cases, the treatment was changed to liposomal amphotericin B. Two cases resulted in surgical resection (18.2%). Clinicians should be aware that bIFDs during voriconazole treatment for IA can occur, and active therapeutic approaches are required in these cases. Oxford University Press 2017-04 2016-08-25 /pmc/articles/PMC5654366/ /pubmed/27562861 http://dx.doi.org/10.1093/mmy/myw067 Text en © The Author 2016. Published by Oxford University Press on behalf of The International Society for Human and Animal Mycology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Kim, Sun Bean Cho, Sung-Yeon Lee, Dong-Gun Choi, Jae-Ki Lee, Hyo-Jin Kim, Si-Hyun Park, Sun Hee Choi, Su-Mi Choi, Jung-Hyun Yoo, Jin-Hong Lee, Jong-Wook Breakthrough invasive fungal diseases during voriconazole treatment for aspergillosis: A 5-year retrospective cohort study |
title | Breakthrough invasive fungal diseases during voriconazole treatment for aspergillosis: A 5-year retrospective cohort study |
title_full | Breakthrough invasive fungal diseases during voriconazole treatment for aspergillosis: A 5-year retrospective cohort study |
title_fullStr | Breakthrough invasive fungal diseases during voriconazole treatment for aspergillosis: A 5-year retrospective cohort study |
title_full_unstemmed | Breakthrough invasive fungal diseases during voriconazole treatment for aspergillosis: A 5-year retrospective cohort study |
title_short | Breakthrough invasive fungal diseases during voriconazole treatment for aspergillosis: A 5-year retrospective cohort study |
title_sort | breakthrough invasive fungal diseases during voriconazole treatment for aspergillosis: a 5-year retrospective cohort study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654366/ https://www.ncbi.nlm.nih.gov/pubmed/27562861 http://dx.doi.org/10.1093/mmy/myw067 |
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