Ceftolozane-tazobactam vs. colistin for the treatment of infections due to multidrug-resistant Pseudomonas aeruginosa: a multicentre cohort study.
Acute Kidney Injury
/ drug therapy
Anti-Bacterial Agents
/ pharmacology
Cephalosporins
Colistin
/ adverse effects
Drug Resistance, Multiple, Bacterial
Female
Humans
Male
Microbial Sensitivity Tests
Pseudomonas Infections
/ drug therapy
Pseudomonas aeruginosa
Retrospective Studies
Tazobactam
/ pharmacology
Ceftolozane-tazobactam
Colistin
Multidrug-resistant
Pseudomonas aeruginosa
Journal
Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459
Informations de publication
Date de publication:
03 2022
03 2022
Historique:
received:
22
11
2021
revised:
08
01
2022
accepted:
23
01
2022
pubmed:
6
2
2022
medline:
6
5
2022
entrez:
5
2
2022
Statut:
ppublish
Résumé
The aim of this study was to compare the safety and effectiveness of ceftolozane-tazobactam (C-T) to colistin-based regimen for treating infections caused by multidrug-resistant (MDR) Pseudomonas aeruginosa. This was a retrospective, multicentre, observational cohort study of inpatients who received either C-T or intravenous colistin for treating infections caused by MDR P. aeruginosa. The study was conducted in five tertiary care hospitals in Saudi Arabia. The main study outcomes included clinical cure at end of treatment, in-hospital mortality, and acute kidney injury (AKI). Univariate analysis and multivariate logistic regression model were conducted to evaluate the independent effect of C-T on the clinical outcome. A total of 184 patients were included in the study: 82 patients received C-T, and 102 patients received colistin-based regimen. Clinical cure (77% vs. 57%; P = 0.005; OR, 2.52; 95% CI, 1.32-4.79) was significantly more common in patients who received C-T. After adjusting the difference between the two groups, treatment with C-T is independently associated with clinical cure (adjusted OR, 2.47; 95% CI, 1.16-5.27). In-hospital mortality (39% vs. 49%; P = 0.175; OR, 0.67; 95% CI, 0.37-1.20) was lower in patients who received C-T, but the difference was not significant. AKI (15% vs. 41%; P < 0.001; OR, 0.25; 95% CI, 0.12-0.51) was significantly less common in patients who received C-T. C-T is associated with a higher rate of clinical cure and lower rate of AKI compared to colistin. Our findings support the preferential use of C-T over colistin-based regimen for treating these infections.
Identifiants
pubmed: 35121161
pii: S2213-7165(22)00027-3
doi: 10.1016/j.jgar.2022.01.023
pii:
doi:
Substances chimiques
Anti-Bacterial Agents
0
Cephalosporins
0
ceftolozane
37A4IES95Q
Tazobactam
SE10G96M8W
Colistin
Z67X93HJG1
Types de publication
Journal Article
Multicenter Study
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
288-294Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no conflict of interest.