Cargando…

1082. Real-World Experience with Omadacycline for Nontuberculous Mycobacterial Infections: A Multicenter Evaluation

BACKGROUND: Nontuberculous mycobacteria (NTM) are resistant to numerous antibiotics and lead to significant morbidity and mortality. Omadacycline (OMC) is an aminomethylcycline antibiotic that is Food and Drug Administration-approved for acute bacterial skin and skin structure infections and communi...

Descripción completa

Detalles Bibliográficos
Autores principales: Morrisette, Taylor, Alosaimy, Sara, Lagnf, Abdalhamid M, Philley, Julie V, Sigler, Carly, Butt, Saira, Kaip, Emily A, MacDougall, Conan, Mejia-Chew, Carlos, Bouchard, Jeannette, Frens, Jeremy J, Gore, Tristan, Hamad, Yasir, Howard, Catessa, Barger, Melissa, Gabriela Cabanilla, M, Ong, Aaron, Veve, Michael P, Webb, Andrew J, Stevens, Ryan W, Cohen, Keira A, Rybak, Michael J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8644900/
http://dx.doi.org/10.1093/ofid/ofab466.1276
_version_ 1784610193042046976
author Morrisette, Taylor
Alosaimy, Sara
Lagnf, Abdalhamid M
Philley, Julie V
Sigler, Carly
Butt, Saira
Kaip, Emily A
MacDougall, Conan
Mejia-Chew, Carlos
Bouchard, Jeannette
Frens, Jeremy J
Gore, Tristan
Hamad, Yasir
Howard, Catessa
Barger, Melissa
Gabriela Cabanilla, M
Ong, Aaron
Veve, Michael P
Webb, Andrew J
Stevens, Ryan W
Cohen, Keira A
Rybak, Michael J
author_facet Morrisette, Taylor
Alosaimy, Sara
Lagnf, Abdalhamid M
Philley, Julie V
Sigler, Carly
Butt, Saira
Kaip, Emily A
MacDougall, Conan
Mejia-Chew, Carlos
Bouchard, Jeannette
Frens, Jeremy J
Gore, Tristan
Hamad, Yasir
Howard, Catessa
Barger, Melissa
Gabriela Cabanilla, M
Ong, Aaron
Veve, Michael P
Webb, Andrew J
Stevens, Ryan W
Cohen, Keira A
Rybak, Michael J
author_sort Morrisette, Taylor
collection PubMed
description BACKGROUND: Nontuberculous mycobacteria (NTM) are resistant to numerous antibiotics and lead to significant morbidity and mortality. Omadacycline (OMC) is an aminomethylcycline antibiotic that is Food and Drug Administration-approved for acute bacterial skin and skin structure infections and community-acquired bacterial pneumonia. Furthermore, OMC has shown in vitro activity against NTM. Given that real-world evidence is lacking, our primary objective was to evaluate the clinical success and tolerability of OMC when used for a variety of NTM infections. METHODS: This was a multicenter, retrospective, observational study conducted from January 2020 to June 2021. We included all patients ≥ 18 years of age that received OMC of any indication for Mycobacterium spp. The primary outcome was clinical success, defined as a lack of all-cause mortality, lack of persistence or re-emergence of infection during or after therapy, and lack of alteration of OMC. Incidence of adverse effects potentially attributable to OMC and reasons for OMC utilization were also analyzed. RESULTS: A total of 31 patients were included from 12 geographically distinct academic health systems (median age: 57 (IQR, 45-63) years; 45% male; 81% Caucasian). The majority of isolated pathogens were Mycobacterium abscessus complex (84%) and of those with subspeciation performed (54%), the majority (86%) were subsp. abscessus. The primary infections were of pulmonary origin (67%) and the median (IQR) duration of OMC therapy was 5.3 (3.2-9.4) months. Most isolates did not have OMC susceptibility conducted (87%), while the majority did for tigecycline (90%). Clinical success was reported in 81% of the population. Most patients were on combination antimicrobial therapy, and 39% of patients reported an adverse effect while on OMC (58% gastrointestinal distress). The majority of patients were prescribed OMC due to ease of administration (61%) and antimicrobial resistance to previous antibiotics (42%). CONCLUSION: OMC may be a potential option for the therapy of NTM infections. Prospective, randomized clinical trials are needed to confirm our preliminary findings. DISCLOSURES: Julie V. Philley, MD, Paratek Pharmaceuticals (Advisor or Review Panel member)Paratek Pharmaceuticals, Inc. (Consultant) Michael P. Veve, Pharm.D., Cumberland (Grant/Research Support)Paratek Pharmaceuticals (Research Grant or Support) Michael J. Rybak, PharmD, MPH, PhD, Paratek Pharmaceuticals (Research Grant or Support)
format Online
Article
Text
id pubmed-8644900
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-86449002021-12-06 1082. Real-World Experience with Omadacycline for Nontuberculous Mycobacterial Infections: A Multicenter Evaluation Morrisette, Taylor Alosaimy, Sara Lagnf, Abdalhamid M Philley, Julie V Sigler, Carly Butt, Saira Kaip, Emily A MacDougall, Conan Mejia-Chew, Carlos Bouchard, Jeannette Frens, Jeremy J Gore, Tristan Hamad, Yasir Howard, Catessa Barger, Melissa Gabriela Cabanilla, M Ong, Aaron Veve, Michael P Webb, Andrew J Stevens, Ryan W Cohen, Keira A Rybak, Michael J Open Forum Infect Dis Poster Abstracts BACKGROUND: Nontuberculous mycobacteria (NTM) are resistant to numerous antibiotics and lead to significant morbidity and mortality. Omadacycline (OMC) is an aminomethylcycline antibiotic that is Food and Drug Administration-approved for acute bacterial skin and skin structure infections and community-acquired bacterial pneumonia. Furthermore, OMC has shown in vitro activity against NTM. Given that real-world evidence is lacking, our primary objective was to evaluate the clinical success and tolerability of OMC when used for a variety of NTM infections. METHODS: This was a multicenter, retrospective, observational study conducted from January 2020 to June 2021. We included all patients ≥ 18 years of age that received OMC of any indication for Mycobacterium spp. The primary outcome was clinical success, defined as a lack of all-cause mortality, lack of persistence or re-emergence of infection during or after therapy, and lack of alteration of OMC. Incidence of adverse effects potentially attributable to OMC and reasons for OMC utilization were also analyzed. RESULTS: A total of 31 patients were included from 12 geographically distinct academic health systems (median age: 57 (IQR, 45-63) years; 45% male; 81% Caucasian). The majority of isolated pathogens were Mycobacterium abscessus complex (84%) and of those with subspeciation performed (54%), the majority (86%) were subsp. abscessus. The primary infections were of pulmonary origin (67%) and the median (IQR) duration of OMC therapy was 5.3 (3.2-9.4) months. Most isolates did not have OMC susceptibility conducted (87%), while the majority did for tigecycline (90%). Clinical success was reported in 81% of the population. Most patients were on combination antimicrobial therapy, and 39% of patients reported an adverse effect while on OMC (58% gastrointestinal distress). The majority of patients were prescribed OMC due to ease of administration (61%) and antimicrobial resistance to previous antibiotics (42%). CONCLUSION: OMC may be a potential option for the therapy of NTM infections. Prospective, randomized clinical trials are needed to confirm our preliminary findings. DISCLOSURES: Julie V. Philley, MD, Paratek Pharmaceuticals (Advisor or Review Panel member)Paratek Pharmaceuticals, Inc. (Consultant) Michael P. Veve, Pharm.D., Cumberland (Grant/Research Support)Paratek Pharmaceuticals (Research Grant or Support) Michael J. Rybak, PharmD, MPH, PhD, Paratek Pharmaceuticals (Research Grant or Support) Oxford University Press 2021-12-04 /pmc/articles/PMC8644900/ http://dx.doi.org/10.1093/ofid/ofab466.1276 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Poster Abstracts
Morrisette, Taylor
Alosaimy, Sara
Lagnf, Abdalhamid M
Philley, Julie V
Sigler, Carly
Butt, Saira
Kaip, Emily A
MacDougall, Conan
Mejia-Chew, Carlos
Bouchard, Jeannette
Frens, Jeremy J
Gore, Tristan
Hamad, Yasir
Howard, Catessa
Barger, Melissa
Gabriela Cabanilla, M
Ong, Aaron
Veve, Michael P
Webb, Andrew J
Stevens, Ryan W
Cohen, Keira A
Rybak, Michael J
1082. Real-World Experience with Omadacycline for Nontuberculous Mycobacterial Infections: A Multicenter Evaluation
title 1082. Real-World Experience with Omadacycline for Nontuberculous Mycobacterial Infections: A Multicenter Evaluation
title_full 1082. Real-World Experience with Omadacycline for Nontuberculous Mycobacterial Infections: A Multicenter Evaluation
title_fullStr 1082. Real-World Experience with Omadacycline for Nontuberculous Mycobacterial Infections: A Multicenter Evaluation
title_full_unstemmed 1082. Real-World Experience with Omadacycline for Nontuberculous Mycobacterial Infections: A Multicenter Evaluation
title_short 1082. Real-World Experience with Omadacycline for Nontuberculous Mycobacterial Infections: A Multicenter Evaluation
title_sort 1082. real-world experience with omadacycline for nontuberculous mycobacterial infections: a multicenter evaluation
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8644900/
http://dx.doi.org/10.1093/ofid/ofab466.1276
work_keys_str_mv AT morrisettetaylor 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT alosaimysara 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT lagnfabdalhamidm 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT philleyjuliev 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT siglercarly 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT buttsaira 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT kaipemilya 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT macdougallconan 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT mejiachewcarlos 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT bouchardjeannette 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT frensjeremyj 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT goretristan 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT hamadyasir 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT howardcatessa 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT bargermelissa 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT gabrielacabanillam 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT ongaaron 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT vevemichaelp 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT webbandrewj 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT stevensryanw 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT cohenkeiraa 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation
AT rybakmichaelj 1082realworldexperiencewithomadacyclinefornontuberculousmycobacterialinfectionsamulticenterevaluation