Ceftazidime-avibactam and comparators against Pseudomonas aeruginosa isolates collected globally and in each geographical region between 2017–2020
dc.contributor.author | Kiratisin P. | |
dc.contributor.author | Kempf M. | |
dc.contributor.author | Stone G. | |
dc.contributor.author | Utt E. | |
dc.contributor.other | Mahidol University | |
dc.date.accessioned | 2023-08-09T18:01:47Z | |
dc.date.available | 2023-08-09T18:01:47Z | |
dc.date.issued | 2023-09-01 | |
dc.description.abstract | Objectives: The objective of this study was to assess the distribution and antimicrobial susceptibility of Pseudomonas aeruginosa isolates against ceftazidime-avibactam (CAZ-AVI) and a panel of comparator agents collected globally and in each region from 2017–2020 from the Antimicrobial Testing Leadership and Surveillance program. Methods: Susceptibility and minimum inhibitory concentration of all P. aeruginosa isolates were determined using broth microdilution methodology according to the Clinical and Laboratory Standards Institute guidelines. Results: Of the total 29746 isolates of P. aeruginosa collected, 20.9% were multidrug resistant (MDR), 20.7% were extremely drug resistant (XDR), 8.4% were CAZ-AVI-resistant (CAZ-AVI-R), and 3.0% were MBL-positive. Amongst the MBL-positive isolates, the proportion of VIM-positive isolates was highest (77.8%). The highest proportion of MDR (25.5%), XDR (25.0%), MBL-positive (5.7%), and CAZ-AVI-R (12.3%) isolates were in Latin America. Amongst the sources, the highest proportion of isolates were from respiratory sources (43.0%), and the majority of isolates were from non-intensive care unit wards (71.2%). Overall, all P. aeruginosa isolates (90.9%) showed high susceptibility to CAZ-AVI. However, MDR and XDR isolates were less susceptible to CAZ-AVI (≤60.7). The only comparators to which all isolates of P. aeruginosa showed good overall susceptibility were colistin (99.1%) and amikacin (90.5%). However, only colistin was active (≥98.3%) against all the resistant isolates. Conclusion: CAZ-AVI presents a potential treatment option against P. aeruginosa infections. However, active monitoring and surveillance, especially of the resistant phenotypes, is warranted for effective treatment of infections caused by P. aeruginosa. | |
dc.identifier.citation | Journal of Global Antimicrobial Resistance Vol.34 (2023) , 113-118 | |
dc.identifier.doi | 10.1016/j.jgar.2023.06.005 | |
dc.identifier.eissn | 22137173 | |
dc.identifier.issn | 22137165 | |
dc.identifier.pmid | 37422001 | |
dc.identifier.scopus | 2-s2.0-85165939880 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/88227 | |
dc.rights.holder | SCOPUS | |
dc.subject | Immunology and Microbiology | |
dc.title | Ceftazidime-avibactam and comparators against Pseudomonas aeruginosa isolates collected globally and in each geographical region between 2017–2020 | |
dc.type | Article | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85165939880&origin=inward | |
oaire.citation.endPage | 118 | |
oaire.citation.startPage | 113 | |
oaire.citation.title | Journal of Global Antimicrobial Resistance | |
oaire.citation.volume | 34 | |
oairecerif.author.affiliation | Siriraj Hospital | |
oairecerif.author.affiliation | Université d’Angers | |
oairecerif.author.affiliation | CHU Angers | |
oairecerif.author.affiliation | Pfizer Inc. |