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Cefiderocol-containing regimens for the treatment of carbapenem-resistant A. baumannii ventilator-associated pneumonia: a propensity-weighted cohort study

BACKGROUND: Cefiderocol is a novel β-lactam with activity against carbapenem-resistant Acinetobacter baumannii (CRAB), but its role in CRAB pulmonary infections is controversial due to limited evidence. OBJECTIVES: To assess the association between cefiderocol-containing regimens treatment and 28-da...

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Autores principales: Rando, Emanuele, Cutuli, Salvatore Lucio, Sangiorgi, Flavio, Tanzarella, Eloisa Sofia, Giovannenze, Francesca, De Angelis, Giulia, Murri, Rita, Antonelli, Massimo, Fantoni, Massimo, De Pascale, Gennaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359102/
https://www.ncbi.nlm.nih.gov/pubmed/37484029
http://dx.doi.org/10.1093/jacamr/dlad085
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author Rando, Emanuele
Cutuli, Salvatore Lucio
Sangiorgi, Flavio
Tanzarella, Eloisa Sofia
Giovannenze, Francesca
De Angelis, Giulia
Murri, Rita
Antonelli, Massimo
Fantoni, Massimo
De Pascale, Gennaro
author_facet Rando, Emanuele
Cutuli, Salvatore Lucio
Sangiorgi, Flavio
Tanzarella, Eloisa Sofia
Giovannenze, Francesca
De Angelis, Giulia
Murri, Rita
Antonelli, Massimo
Fantoni, Massimo
De Pascale, Gennaro
author_sort Rando, Emanuele
collection PubMed
description BACKGROUND: Cefiderocol is a novel β-lactam with activity against carbapenem-resistant Acinetobacter baumannii (CRAB), but its role in CRAB pulmonary infections is controversial due to limited evidence. OBJECTIVES: To assess the association between cefiderocol-containing regimens treatment and 28-day mortality in carbapenem-resistant A. baumannii ventilator-associated pneumonia (VAP). METHODS: An observational cohort study including critically ill COVID-19 patients with CRAB-VAP admitted to two ICUs of a large academic hospital in Rome between September 2020 and December 2022. The primary outcome was 28-day all-cause mortality. A propensity score was created to balance the cefiderocol- and non-cefiderocol-containing groups. A propensity-weighted multiple logistic regression model was calculated to evaluate risk factors for 28-day mortality. Survival curves were calculated using the Kaplan–Meier method. RESULTS: 121 patients were enrolled, 55 were treated with cefiderocol- and 66 with non-cefiderocol-containing regimens. The 28-day all-cause mortality was 56% (68/121). A statistically significant difference in 28-day mortality was found between cefiderocol- and non-cefiderocol- containing regimens groups (44% versus 67%, P = 0.011). In the propensity-adjusted multiple logistic regression, cefiderocol (OR 0.35 95% CI 0.14, 0.83) was a predictor of 28-day survival, Charlson comorbidity index (OR 1.36 95% CI 1.16, 1.78), SOFA score (OR 1.24 95% CI 1.09, 1.57) and septic shock (OR 3.71 95% CI 1.44, 12.73) were all associated with increased 28-day mortality. CONCLUSION: Cefiderocol-containing regimens were associated with reduced 28-day mortality in CRAB-VAP. The sample size and the observational design limit the study’s conclusions. Future RCTs are needed to establish cefiderocol’s definite role in these infections.
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spelling pubmed-103591022023-07-21 Cefiderocol-containing regimens for the treatment of carbapenem-resistant A. baumannii ventilator-associated pneumonia: a propensity-weighted cohort study Rando, Emanuele Cutuli, Salvatore Lucio Sangiorgi, Flavio Tanzarella, Eloisa Sofia Giovannenze, Francesca De Angelis, Giulia Murri, Rita Antonelli, Massimo Fantoni, Massimo De Pascale, Gennaro JAC Antimicrob Resist Original Article BACKGROUND: Cefiderocol is a novel β-lactam with activity against carbapenem-resistant Acinetobacter baumannii (CRAB), but its role in CRAB pulmonary infections is controversial due to limited evidence. OBJECTIVES: To assess the association between cefiderocol-containing regimens treatment and 28-day mortality in carbapenem-resistant A. baumannii ventilator-associated pneumonia (VAP). METHODS: An observational cohort study including critically ill COVID-19 patients with CRAB-VAP admitted to two ICUs of a large academic hospital in Rome between September 2020 and December 2022. The primary outcome was 28-day all-cause mortality. A propensity score was created to balance the cefiderocol- and non-cefiderocol-containing groups. A propensity-weighted multiple logistic regression model was calculated to evaluate risk factors for 28-day mortality. Survival curves were calculated using the Kaplan–Meier method. RESULTS: 121 patients were enrolled, 55 were treated with cefiderocol- and 66 with non-cefiderocol-containing regimens. The 28-day all-cause mortality was 56% (68/121). A statistically significant difference in 28-day mortality was found between cefiderocol- and non-cefiderocol- containing regimens groups (44% versus 67%, P = 0.011). In the propensity-adjusted multiple logistic regression, cefiderocol (OR 0.35 95% CI 0.14, 0.83) was a predictor of 28-day survival, Charlson comorbidity index (OR 1.36 95% CI 1.16, 1.78), SOFA score (OR 1.24 95% CI 1.09, 1.57) and septic shock (OR 3.71 95% CI 1.44, 12.73) were all associated with increased 28-day mortality. CONCLUSION: Cefiderocol-containing regimens were associated with reduced 28-day mortality in CRAB-VAP. The sample size and the observational design limit the study’s conclusions. Future RCTs are needed to establish cefiderocol’s definite role in these infections. Oxford University Press 2023-07-20 /pmc/articles/PMC10359102/ /pubmed/37484029 http://dx.doi.org/10.1093/jacamr/dlad085 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Rando, Emanuele
Cutuli, Salvatore Lucio
Sangiorgi, Flavio
Tanzarella, Eloisa Sofia
Giovannenze, Francesca
De Angelis, Giulia
Murri, Rita
Antonelli, Massimo
Fantoni, Massimo
De Pascale, Gennaro
Cefiderocol-containing regimens for the treatment of carbapenem-resistant A. baumannii ventilator-associated pneumonia: a propensity-weighted cohort study
title Cefiderocol-containing regimens for the treatment of carbapenem-resistant A. baumannii ventilator-associated pneumonia: a propensity-weighted cohort study
title_full Cefiderocol-containing regimens for the treatment of carbapenem-resistant A. baumannii ventilator-associated pneumonia: a propensity-weighted cohort study
title_fullStr Cefiderocol-containing regimens for the treatment of carbapenem-resistant A. baumannii ventilator-associated pneumonia: a propensity-weighted cohort study
title_full_unstemmed Cefiderocol-containing regimens for the treatment of carbapenem-resistant A. baumannii ventilator-associated pneumonia: a propensity-weighted cohort study
title_short Cefiderocol-containing regimens for the treatment of carbapenem-resistant A. baumannii ventilator-associated pneumonia: a propensity-weighted cohort study
title_sort cefiderocol-containing regimens for the treatment of carbapenem-resistant a. baumannii ventilator-associated pneumonia: a propensity-weighted cohort study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359102/
https://www.ncbi.nlm.nih.gov/pubmed/37484029
http://dx.doi.org/10.1093/jacamr/dlad085
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