Antimicrobial activity of ceftolozane/tazobactam tested against contemporary (2015–2017) Pseudomonas aeruginosa isolates from a global surveillance programme

Objectives: Ceftolozane/tazobactam (C–T) is an antimicrobial combination of an antipseudomonal cephalosporin and a β-lactamase inhibitor. C–T has been approved in >60 countries for complicated urinary tract infections, acute pyelonephritis, complicated intra-abdominal infections in combination wi...

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Main Authors: Dee Shortridge, Michael A. Pfaller, Jennifer M. Streit, Robert K. Flamm
Format: Article
Language:English
Published: Elsevier 2020-06-01
Series:Journal of Global Antimicrobial Resistance
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213716519302632
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spelling doaj-f9f25171ea5b49a39a00b5372e73e4b92021-05-20T07:48:47ZengElsevierJournal of Global Antimicrobial Resistance2213-71652020-06-01216064Antimicrobial activity of ceftolozane/tazobactam tested against contemporary (2015–2017) Pseudomonas aeruginosa isolates from a global surveillance programmeDee Shortridge0Michael A. Pfaller1Jennifer M. Streit2Robert K. Flamm3Corresponding author.; JMI Laboratories, 345 Beaver Kreek Centre, Suite A, North Liberty, IA 52317, USAJMI Laboratories, 345 Beaver Kreek Centre, Suite A, North Liberty, IA 52317, USAJMI Laboratories, 345 Beaver Kreek Centre, Suite A, North Liberty, IA 52317, USAJMI Laboratories, 345 Beaver Kreek Centre, Suite A, North Liberty, IA 52317, USAObjectives: Ceftolozane/tazobactam (C–T) is an antimicrobial combination of an antipseudomonal cephalosporin and a β-lactamase inhibitor. C–T has been approved in >60 countries for complicated urinary tract infections, acute pyelonephritis, complicated intra-abdominal infections in combination with metronidazole, and was recently approved for hospital-acquired bacterial pneumonia. In this study, data for Pseudomonas aeruginosa isolates consecutively collected from various infection types in hospitalised patients from 2015 to 2017 were analysed. Methods: A total of 6836 P. aeruginosa isolates were collected from 104 hospitals in four continents and were tested for susceptibility to C–T by CLSI broth microdilution methodology at JMI Laboratories using CLSI (2018) breakpoints. Other agents tested included amikacin, ceftazidime (CAZ), colistin (COL), levofloxacin (LVX), meropenem (MEM) and piperacillin/tazobactam (TZP). Resistance phenotypes analysed included CAZ-non-susceptible (CAZ-NS), COL-NS, MEM-NS, LVX-NS, TZP-NS and β-lactam-NS. Multidrug resistance (MDR) was defined as NS to ≥1 drug in ≥3 drug classes, and extensively drug-resistant (XDR) was defined as NS to ≥1 agent in all but 2 or fewer antimicrobial classes. Results: The most common infection from which P. aeruginosa was isolated was pneumonia (51.6%), followed by skin and skin-structure infection (22.2%) and bloodstream infection (15.3%). Percentage susceptibility to C–T varied by region: 98.2% in North America; 94.8% in Asia-Pacific; 90.8% in Latin America; and 89.1% in Europe. Conclusion: C–T had potent activity against P. aeruginosa isolated from patients in hospitals in four continents. C–T was more active than all comparators, except COL, and maintained activity against MDR and XDR isolates and isolates NS to all four tested β-lactams. C–T was active against 13/16 COL-NS isolates.http://www.sciencedirect.com/science/article/pii/S2213716519302632Pseudomonas aeruginosaCeftolozane/tazobactamGlobal surveillance
collection DOAJ
language English
format Article
sources DOAJ
author Dee Shortridge
Michael A. Pfaller
Jennifer M. Streit
Robert K. Flamm
spellingShingle Dee Shortridge
Michael A. Pfaller
Jennifer M. Streit
Robert K. Flamm
Antimicrobial activity of ceftolozane/tazobactam tested against contemporary (2015–2017) Pseudomonas aeruginosa isolates from a global surveillance programme
Journal of Global Antimicrobial Resistance
Pseudomonas aeruginosa
Ceftolozane/tazobactam
Global surveillance
author_facet Dee Shortridge
Michael A. Pfaller
Jennifer M. Streit
Robert K. Flamm
author_sort Dee Shortridge
title Antimicrobial activity of ceftolozane/tazobactam tested against contemporary (2015–2017) Pseudomonas aeruginosa isolates from a global surveillance programme
title_short Antimicrobial activity of ceftolozane/tazobactam tested against contemporary (2015–2017) Pseudomonas aeruginosa isolates from a global surveillance programme
title_full Antimicrobial activity of ceftolozane/tazobactam tested against contemporary (2015–2017) Pseudomonas aeruginosa isolates from a global surveillance programme
title_fullStr Antimicrobial activity of ceftolozane/tazobactam tested against contemporary (2015–2017) Pseudomonas aeruginosa isolates from a global surveillance programme
title_full_unstemmed Antimicrobial activity of ceftolozane/tazobactam tested against contemporary (2015–2017) Pseudomonas aeruginosa isolates from a global surveillance programme
title_sort antimicrobial activity of ceftolozane/tazobactam tested against contemporary (2015–2017) pseudomonas aeruginosa isolates from a global surveillance programme
publisher Elsevier
series Journal of Global Antimicrobial Resistance
issn 2213-7165
publishDate 2020-06-01
description Objectives: Ceftolozane/tazobactam (C–T) is an antimicrobial combination of an antipseudomonal cephalosporin and a β-lactamase inhibitor. C–T has been approved in >60 countries for complicated urinary tract infections, acute pyelonephritis, complicated intra-abdominal infections in combination with metronidazole, and was recently approved for hospital-acquired bacterial pneumonia. In this study, data for Pseudomonas aeruginosa isolates consecutively collected from various infection types in hospitalised patients from 2015 to 2017 were analysed. Methods: A total of 6836 P. aeruginosa isolates were collected from 104 hospitals in four continents and were tested for susceptibility to C–T by CLSI broth microdilution methodology at JMI Laboratories using CLSI (2018) breakpoints. Other agents tested included amikacin, ceftazidime (CAZ), colistin (COL), levofloxacin (LVX), meropenem (MEM) and piperacillin/tazobactam (TZP). Resistance phenotypes analysed included CAZ-non-susceptible (CAZ-NS), COL-NS, MEM-NS, LVX-NS, TZP-NS and β-lactam-NS. Multidrug resistance (MDR) was defined as NS to ≥1 drug in ≥3 drug classes, and extensively drug-resistant (XDR) was defined as NS to ≥1 agent in all but 2 or fewer antimicrobial classes. Results: The most common infection from which P. aeruginosa was isolated was pneumonia (51.6%), followed by skin and skin-structure infection (22.2%) and bloodstream infection (15.3%). Percentage susceptibility to C–T varied by region: 98.2% in North America; 94.8% in Asia-Pacific; 90.8% in Latin America; and 89.1% in Europe. Conclusion: C–T had potent activity against P. aeruginosa isolated from patients in hospitals in four continents. C–T was more active than all comparators, except COL, and maintained activity against MDR and XDR isolates and isolates NS to all four tested β-lactams. C–T was active against 13/16 COL-NS isolates.
topic Pseudomonas aeruginosa
Ceftolozane/tazobactam
Global surveillance
url http://www.sciencedirect.com/science/article/pii/S2213716519302632
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