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2395. Mechanism-Based-Susceptibility Testing (MBST) Using Disc Diffusion Assays (DDA) to Guide Treatment of Multidrug- and Extensively Drug-Resistant Pseudomonas aeruginosa (MDR-XDR-Pa) in a Cystic Fibrosis (CF) Lung Transplant Recipient; Are We Ready for Combination Therapy vs. MDR-XDR-Pa?

BACKGROUND: Lung infections with MDR-XDR-Pa in patients with CF are challenging due to the emergence of antibiotic resistance. We applied MBST with DDA to guide combination antibiotic therapy in an 18-year-old woman with CF. We investigated if this approach can assist in choosing effective regimens....

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Autores principales: Abbo, Lilian M, Yasmin, Mohamad, Marshall, Steven H, Perez, Federico, Corzo-Pedrosa, Mónica, Camargo, Jose F, Simkins, Jacques, Aragon, Laura, Anjan, Shweta, Morris, Michele I, Brozzi, Nicolas, Loebe, Mathias, Fulmer, Jesse, Sinha, Neeraj, Martinez, Octavio, Perez-Cardona, Armando, Colin, Andrew, Cloke, Christina, Bonomo, Robert A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255010/
http://dx.doi.org/10.1093/ofid/ofy210.2048
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author Abbo, Lilian M
Yasmin, Mohamad
Marshall, Steven H
Perez, Federico
Corzo-Pedrosa, Mónica
Camargo, Jose F
Simkins, Jacques
Aragon, Laura
Anjan, Shweta
Morris, Michele I
Brozzi, Nicolas
Loebe, Mathias
Fulmer, Jesse
Sinha, Neeraj
Martinez, Octavio
Perez-Cardona, Armando
Colin, Andrew
Cloke, Christina
Bonomo, Robert A
author_facet Abbo, Lilian M
Yasmin, Mohamad
Marshall, Steven H
Perez, Federico
Corzo-Pedrosa, Mónica
Camargo, Jose F
Simkins, Jacques
Aragon, Laura
Anjan, Shweta
Morris, Michele I
Brozzi, Nicolas
Loebe, Mathias
Fulmer, Jesse
Sinha, Neeraj
Martinez, Octavio
Perez-Cardona, Armando
Colin, Andrew
Cloke, Christina
Bonomo, Robert A
author_sort Abbo, Lilian M
collection PubMed
description BACKGROUND: Lung infections with MDR-XDR-Pa in patients with CF are challenging due to the emergence of antibiotic resistance. We applied MBST with DDA to guide combination antibiotic therapy in an 18-year-old woman with CF. We investigated if this approach can assist in choosing effective regimens. METHODS: Consecutive Pa respiratory isolates were collected between 12/16 and 3/18 and typed with MLST. After automated antibiotic susceptibility (AST) and Kirby-Bauer testing, we performed double or triple DDAs. Combinations were based on mechanisms (MBST) of anti-pseudomonal antibiotics (e.g., targeting of penicillin-binding proteins, β-lactamase inhibition, and cell membrane disruption). RESULTS: During therapy, 1859 antibiotic-days were administered. Fifteen Pa isolates, (9 sequence type (ST) 2100 and 1 ST463) with varying AST patterns were found (figure). MBST with DDA revealed active combinations for isolates resistant to individual antibiotics (table). These combinations led to a microbiological response permitting lung transplantation. Antibiotic regimens were also informed by allergies, clinical and radiologic findings. CONCLUSION: Strains with evolving resistance profiles recapitulate the dynamic nature of respiratory infections in CF. Double or triple DDAs identified potential treatment options, e.g., vs. MDR-XDR Pa. MBST can support the management of challenging infections. Table: Antimicrobial combinations reflecting zones of inhibition by strain and date. CZA: ceftazidime–avibactam; C/T: ceftolozane-tazobactam; TOB: tobramycin; PMB: polymyxin B; FOF: fosfomycin; TZP: piperacillin–tazobactam; CIP: ciprofloxacin; IPM: imipenem; MEM: meropenem. Bold: largest zone [Image: see text] DISCLOSURES: L. M. Abbo, Roche Diagnostics: Scientific Advisor, Consulting fee. M. I. Morris, Chimerix: Investigator and Scientific Advisor, Consulting fee and Research support. Merck: Investigator, Research grant.
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spelling pubmed-62550102018-11-28 2395. Mechanism-Based-Susceptibility Testing (MBST) Using Disc Diffusion Assays (DDA) to Guide Treatment of Multidrug- and Extensively Drug-Resistant Pseudomonas aeruginosa (MDR-XDR-Pa) in a Cystic Fibrosis (CF) Lung Transplant Recipient; Are We Ready for Combination Therapy vs. MDR-XDR-Pa? Abbo, Lilian M Yasmin, Mohamad Marshall, Steven H Perez, Federico Corzo-Pedrosa, Mónica Camargo, Jose F Simkins, Jacques Aragon, Laura Anjan, Shweta Morris, Michele I Brozzi, Nicolas Loebe, Mathias Fulmer, Jesse Sinha, Neeraj Martinez, Octavio Perez-Cardona, Armando Colin, Andrew Cloke, Christina Bonomo, Robert A Open Forum Infect Dis Abstracts BACKGROUND: Lung infections with MDR-XDR-Pa in patients with CF are challenging due to the emergence of antibiotic resistance. We applied MBST with DDA to guide combination antibiotic therapy in an 18-year-old woman with CF. We investigated if this approach can assist in choosing effective regimens. METHODS: Consecutive Pa respiratory isolates were collected between 12/16 and 3/18 and typed with MLST. After automated antibiotic susceptibility (AST) and Kirby-Bauer testing, we performed double or triple DDAs. Combinations were based on mechanisms (MBST) of anti-pseudomonal antibiotics (e.g., targeting of penicillin-binding proteins, β-lactamase inhibition, and cell membrane disruption). RESULTS: During therapy, 1859 antibiotic-days were administered. Fifteen Pa isolates, (9 sequence type (ST) 2100 and 1 ST463) with varying AST patterns were found (figure). MBST with DDA revealed active combinations for isolates resistant to individual antibiotics (table). These combinations led to a microbiological response permitting lung transplantation. Antibiotic regimens were also informed by allergies, clinical and radiologic findings. CONCLUSION: Strains with evolving resistance profiles recapitulate the dynamic nature of respiratory infections in CF. Double or triple DDAs identified potential treatment options, e.g., vs. MDR-XDR Pa. MBST can support the management of challenging infections. Table: Antimicrobial combinations reflecting zones of inhibition by strain and date. CZA: ceftazidime–avibactam; C/T: ceftolozane-tazobactam; TOB: tobramycin; PMB: polymyxin B; FOF: fosfomycin; TZP: piperacillin–tazobactam; CIP: ciprofloxacin; IPM: imipenem; MEM: meropenem. Bold: largest zone [Image: see text] DISCLOSURES: L. M. Abbo, Roche Diagnostics: Scientific Advisor, Consulting fee. M. I. Morris, Chimerix: Investigator and Scientific Advisor, Consulting fee and Research support. Merck: Investigator, Research grant. Oxford University Press 2018-11-26 /pmc/articles/PMC6255010/ http://dx.doi.org/10.1093/ofid/ofy210.2048 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
Abbo, Lilian M
Yasmin, Mohamad
Marshall, Steven H
Perez, Federico
Corzo-Pedrosa, Mónica
Camargo, Jose F
Simkins, Jacques
Aragon, Laura
Anjan, Shweta
Morris, Michele I
Brozzi, Nicolas
Loebe, Mathias
Fulmer, Jesse
Sinha, Neeraj
Martinez, Octavio
Perez-Cardona, Armando
Colin, Andrew
Cloke, Christina
Bonomo, Robert A
2395. Mechanism-Based-Susceptibility Testing (MBST) Using Disc Diffusion Assays (DDA) to Guide Treatment of Multidrug- and Extensively Drug-Resistant Pseudomonas aeruginosa (MDR-XDR-Pa) in a Cystic Fibrosis (CF) Lung Transplant Recipient; Are We Ready for Combination Therapy vs. MDR-XDR-Pa?
title 2395. Mechanism-Based-Susceptibility Testing (MBST) Using Disc Diffusion Assays (DDA) to Guide Treatment of Multidrug- and Extensively Drug-Resistant Pseudomonas aeruginosa (MDR-XDR-Pa) in a Cystic Fibrosis (CF) Lung Transplant Recipient; Are We Ready for Combination Therapy vs. MDR-XDR-Pa?
title_full 2395. Mechanism-Based-Susceptibility Testing (MBST) Using Disc Diffusion Assays (DDA) to Guide Treatment of Multidrug- and Extensively Drug-Resistant Pseudomonas aeruginosa (MDR-XDR-Pa) in a Cystic Fibrosis (CF) Lung Transplant Recipient; Are We Ready for Combination Therapy vs. MDR-XDR-Pa?
title_fullStr 2395. Mechanism-Based-Susceptibility Testing (MBST) Using Disc Diffusion Assays (DDA) to Guide Treatment of Multidrug- and Extensively Drug-Resistant Pseudomonas aeruginosa (MDR-XDR-Pa) in a Cystic Fibrosis (CF) Lung Transplant Recipient; Are We Ready for Combination Therapy vs. MDR-XDR-Pa?
title_full_unstemmed 2395. Mechanism-Based-Susceptibility Testing (MBST) Using Disc Diffusion Assays (DDA) to Guide Treatment of Multidrug- and Extensively Drug-Resistant Pseudomonas aeruginosa (MDR-XDR-Pa) in a Cystic Fibrosis (CF) Lung Transplant Recipient; Are We Ready for Combination Therapy vs. MDR-XDR-Pa?
title_short 2395. Mechanism-Based-Susceptibility Testing (MBST) Using Disc Diffusion Assays (DDA) to Guide Treatment of Multidrug- and Extensively Drug-Resistant Pseudomonas aeruginosa (MDR-XDR-Pa) in a Cystic Fibrosis (CF) Lung Transplant Recipient; Are We Ready for Combination Therapy vs. MDR-XDR-Pa?
title_sort 2395. mechanism-based-susceptibility testing (mbst) using disc diffusion assays (dda) to guide treatment of multidrug- and extensively drug-resistant pseudomonas aeruginosa (mdr-xdr-pa) in a cystic fibrosis (cf) lung transplant recipient; are we ready for combination therapy vs. mdr-xdr-pa?
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255010/
http://dx.doi.org/10.1093/ofid/ofy210.2048
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