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357. Aspergillus Isolates Remain Largely Susceptible to Azoles and Other Antifungals at a Large Transplant Program Using Azole Prophylaxis

BACKGROUND: The emergence of azole resistance globally among Aspergillus species has major clinical and agricultural implications. At our center, isavuconazole (ISA), posaconazole (POS), and voriconazole (VOR) have been used as antifungal prophylaxis in solid-organ transplant recipients. We determin...

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Autores principales: Driscoll, Eileen, Clancy, Cornelius J, Squires, Kevin, Shields, Ryan K, Nguyen, Minh-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253242/
http://dx.doi.org/10.1093/ofid/ofy210.368
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author Driscoll, Eileen
Clancy, Cornelius J
Squires, Kevin
Shields, Ryan K
Nguyen, Minh-Hong
author_facet Driscoll, Eileen
Clancy, Cornelius J
Squires, Kevin
Shields, Ryan K
Nguyen, Minh-Hong
author_sort Driscoll, Eileen
collection PubMed
description BACKGROUND: The emergence of azole resistance globally among Aspergillus species has major clinical and agricultural implications. At our center, isavuconazole (ISA), posaconazole (POS), and voriconazole (VOR) have been used as antifungal prophylaxis in solid-organ transplant recipients. We determined susceptibility to azoles and other antifungals among Aspergillus isolates from our center. METHODS: Fifty-two patient isolates of Aspergillus species were collected from the UPMC Microbiology Laboratory between December 2016 and April 2018. Minimum inhibitory concentrations (MICs) of ISA, POS, VOR, amphotericin B (AmB), and caspofungin (CAS) were measured using EUCAST Antimicrobial Susceptibility Testing methods. Candida parapsilosis ATCC 22019 and Candida krusei ATCC 6258 were used as quality control. RESULTS: Seventy-one percent (37/52) of isolates were from solid-organ transplant recipients (34 lungs, two liver, and one heart). Aspergillus spp. were A. fumigatus (29), A. terreus (At, 6), A. niger, A. flavus and Aspergillus calidoustus (five of each species), and A. lentulus and A. thermomutatus (one of each species). Thirteen breakthrough (BT) isolates were recovered from patients on azoles: A. calidoustus (5), A. niger (4), A. flavus (2), A. fumigatus (1) and At (1). A. calidoustus, A. flavus, and A. niger were more likely than other species to be recovered from azole BT (75% (12/16) vs. 5% (2/36), P = 0.06). For all isolates, ISA, VOR, and POSA MIC(50) were 0.25 µg/mL, 0.04 µg/mL, and 0.25 µg/mL, respectively. One A. calidoustus and one At were resistant to all antifungals (azoles, AmB, and caspofungin MICs were >16 µg/mL); both were associated with azole BT. ISA, POS, and VOR MIC(50) vs. azole BT isolates (0.5, 0.125, and 0.5 µg/mL, respectively) were higher than those vs. non-BT isolates (0.25, 0.03, and 0.25 µg/mL, respectively; P < 0.01 for all). CONCLUSION: Despite widespread use of azole prophylaxis in transplant recipients at our center, we did not observe high rates of resistance to azoles or other antifungals among Aspergillus isolates, although azole MICs were higher against BT isolates. Azole BT isolates were more likely to be non-A. fumigatus species. Clinicians should understand that antifungal resistance rates can vary by center and geographical location, and use their local epidemiology to guide decisions about the utility of specific agents in their populations. [Image: see text] DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62532422018-11-28 357. Aspergillus Isolates Remain Largely Susceptible to Azoles and Other Antifungals at a Large Transplant Program Using Azole Prophylaxis Driscoll, Eileen Clancy, Cornelius J Squires, Kevin Shields, Ryan K Nguyen, Minh-Hong Open Forum Infect Dis Abstracts BACKGROUND: The emergence of azole resistance globally among Aspergillus species has major clinical and agricultural implications. At our center, isavuconazole (ISA), posaconazole (POS), and voriconazole (VOR) have been used as antifungal prophylaxis in solid-organ transplant recipients. We determined susceptibility to azoles and other antifungals among Aspergillus isolates from our center. METHODS: Fifty-two patient isolates of Aspergillus species were collected from the UPMC Microbiology Laboratory between December 2016 and April 2018. Minimum inhibitory concentrations (MICs) of ISA, POS, VOR, amphotericin B (AmB), and caspofungin (CAS) were measured using EUCAST Antimicrobial Susceptibility Testing methods. Candida parapsilosis ATCC 22019 and Candida krusei ATCC 6258 were used as quality control. RESULTS: Seventy-one percent (37/52) of isolates were from solid-organ transplant recipients (34 lungs, two liver, and one heart). Aspergillus spp. were A. fumigatus (29), A. terreus (At, 6), A. niger, A. flavus and Aspergillus calidoustus (five of each species), and A. lentulus and A. thermomutatus (one of each species). Thirteen breakthrough (BT) isolates were recovered from patients on azoles: A. calidoustus (5), A. niger (4), A. flavus (2), A. fumigatus (1) and At (1). A. calidoustus, A. flavus, and A. niger were more likely than other species to be recovered from azole BT (75% (12/16) vs. 5% (2/36), P = 0.06). For all isolates, ISA, VOR, and POSA MIC(50) were 0.25 µg/mL, 0.04 µg/mL, and 0.25 µg/mL, respectively. One A. calidoustus and one At were resistant to all antifungals (azoles, AmB, and caspofungin MICs were >16 µg/mL); both were associated with azole BT. ISA, POS, and VOR MIC(50) vs. azole BT isolates (0.5, 0.125, and 0.5 µg/mL, respectively) were higher than those vs. non-BT isolates (0.25, 0.03, and 0.25 µg/mL, respectively; P < 0.01 for all). CONCLUSION: Despite widespread use of azole prophylaxis in transplant recipients at our center, we did not observe high rates of resistance to azoles or other antifungals among Aspergillus isolates, although azole MICs were higher against BT isolates. Azole BT isolates were more likely to be non-A. fumigatus species. Clinicians should understand that antifungal resistance rates can vary by center and geographical location, and use their local epidemiology to guide decisions about the utility of specific agents in their populations. [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6253242/ http://dx.doi.org/10.1093/ofid/ofy210.368 Text en © The Author(s) 2018. 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 Abstracts
Driscoll, Eileen
Clancy, Cornelius J
Squires, Kevin
Shields, Ryan K
Nguyen, Minh-Hong
357. Aspergillus Isolates Remain Largely Susceptible to Azoles and Other Antifungals at a Large Transplant Program Using Azole Prophylaxis
title 357. Aspergillus Isolates Remain Largely Susceptible to Azoles and Other Antifungals at a Large Transplant Program Using Azole Prophylaxis
title_full 357. Aspergillus Isolates Remain Largely Susceptible to Azoles and Other Antifungals at a Large Transplant Program Using Azole Prophylaxis
title_fullStr 357. Aspergillus Isolates Remain Largely Susceptible to Azoles and Other Antifungals at a Large Transplant Program Using Azole Prophylaxis
title_full_unstemmed 357. Aspergillus Isolates Remain Largely Susceptible to Azoles and Other Antifungals at a Large Transplant Program Using Azole Prophylaxis
title_short 357. Aspergillus Isolates Remain Largely Susceptible to Azoles and Other Antifungals at a Large Transplant Program Using Azole Prophylaxis
title_sort 357. aspergillus isolates remain largely susceptible to azoles and other antifungals at a large transplant program using azole prophylaxis
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253242/
http://dx.doi.org/10.1093/ofid/ofy210.368
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