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Omadacycline for the Treatment of Mycobacterium abscessus Disease: A Case Series

BACKGROUND: Omadacycline is an aminomethylcycline antimicrobial approved by the US Food and Drug Administration in 2018 for community-acquired bacterial pneumonia and acute bacterial skin and skin structure infections. It has in vitro activity against nontuberculous mycobacteria, including Mycobacte...

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Autores principales: Pearson, Jeffrey C, Dionne, Brandon, Richterman, Aaron, Vidal, Samuel J, Weiss, Zoe, Velásquez, Gustavo E, Marty, Francisco M, Sax, Paul E, Yawetz, Sigal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566545/
https://www.ncbi.nlm.nih.gov/pubmed/33094118
http://dx.doi.org/10.1093/ofid/ofaa415
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author Pearson, Jeffrey C
Dionne, Brandon
Richterman, Aaron
Vidal, Samuel J
Weiss, Zoe
Velásquez, Gustavo E
Marty, Francisco M
Sax, Paul E
Yawetz, Sigal
author_facet Pearson, Jeffrey C
Dionne, Brandon
Richterman, Aaron
Vidal, Samuel J
Weiss, Zoe
Velásquez, Gustavo E
Marty, Francisco M
Sax, Paul E
Yawetz, Sigal
author_sort Pearson, Jeffrey C
collection PubMed
description BACKGROUND: Omadacycline is an aminomethylcycline antimicrobial approved by the US Food and Drug Administration in 2018 for community-acquired bacterial pneumonia and acute bacterial skin and skin structure infections. It has in vitro activity against nontuberculous mycobacteria, including Mycobacterium abscessus complex, but clinical data for this indication are lacking. METHODS: Omadacycline use was reviewed at an 804-bed academic medical center. Patients were included if they received omadacycline for culture-proven M abscessus disease in 2019. RESULTS: Four patients received omadacycline for the treatment of culture-positive M abscessus disease in 2019. Two patients had cutaneous disease, 1 had pulmonary disease, and 1 had osteomyelitis and bacteremia. The patients received omadacycline for a median duration of 166 days (range, 104–227) along with a combination of other antimicrobial agents. Omadacycline-containing regimens were associated with a clinical cure in 3 of 4 patients, with 1 patient improving on ongoing treatment. Omadacycline’s tolerability was acceptable for patients with M abscessus disease, with 1 patient discontinuing therapy in month 6 due to nausea. CONCLUSIONS: Omadacycline is a novel oral option for the treatment of M abscessus disease, for which safe and effective options are needed. Although this case series is promising, further data are required to determine omadacycline’s definitive role in the treatment of M abscessus disease.
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spelling pubmed-75665452020-10-21 Omadacycline for the Treatment of Mycobacterium abscessus Disease: A Case Series Pearson, Jeffrey C Dionne, Brandon Richterman, Aaron Vidal, Samuel J Weiss, Zoe Velásquez, Gustavo E Marty, Francisco M Sax, Paul E Yawetz, Sigal Open Forum Infect Dis Major Articles BACKGROUND: Omadacycline is an aminomethylcycline antimicrobial approved by the US Food and Drug Administration in 2018 for community-acquired bacterial pneumonia and acute bacterial skin and skin structure infections. It has in vitro activity against nontuberculous mycobacteria, including Mycobacterium abscessus complex, but clinical data for this indication are lacking. METHODS: Omadacycline use was reviewed at an 804-bed academic medical center. Patients were included if they received omadacycline for culture-proven M abscessus disease in 2019. RESULTS: Four patients received omadacycline for the treatment of culture-positive M abscessus disease in 2019. Two patients had cutaneous disease, 1 had pulmonary disease, and 1 had osteomyelitis and bacteremia. The patients received omadacycline for a median duration of 166 days (range, 104–227) along with a combination of other antimicrobial agents. Omadacycline-containing regimens were associated with a clinical cure in 3 of 4 patients, with 1 patient improving on ongoing treatment. Omadacycline’s tolerability was acceptable for patients with M abscessus disease, with 1 patient discontinuing therapy in month 6 due to nausea. CONCLUSIONS: Omadacycline is a novel oral option for the treatment of M abscessus disease, for which safe and effective options are needed. Although this case series is promising, further data are required to determine omadacycline’s definitive role in the treatment of M abscessus disease. Oxford University Press 2020-09-09 /pmc/articles/PMC7566545/ /pubmed/33094118 http://dx.doi.org/10.1093/ofid/ofaa415 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Articles
Pearson, Jeffrey C
Dionne, Brandon
Richterman, Aaron
Vidal, Samuel J
Weiss, Zoe
Velásquez, Gustavo E
Marty, Francisco M
Sax, Paul E
Yawetz, Sigal
Omadacycline for the Treatment of Mycobacterium abscessus Disease: A Case Series
title Omadacycline for the Treatment of Mycobacterium abscessus Disease: A Case Series
title_full Omadacycline for the Treatment of Mycobacterium abscessus Disease: A Case Series
title_fullStr Omadacycline for the Treatment of Mycobacterium abscessus Disease: A Case Series
title_full_unstemmed Omadacycline for the Treatment of Mycobacterium abscessus Disease: A Case Series
title_short Omadacycline for the Treatment of Mycobacterium abscessus Disease: A Case Series
title_sort omadacycline for the treatment of mycobacterium abscessus disease: a case series
topic Major Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566545/
https://www.ncbi.nlm.nih.gov/pubmed/33094118
http://dx.doi.org/10.1093/ofid/ofaa415
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