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Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: A Multicenter Study
BACKGROUND: Multidrug-resistant Pseudomonas aeruginosa infections remain common in hospitals worldwide. We investigated the outcomes associated with the use of ceftolozane-tazobactam for the treatment of these infections. METHODS: Data were collected retrospectively from 20 hospitals across the Unit...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247659/ https://www.ncbi.nlm.nih.gov/pubmed/30488041 http://dx.doi.org/10.1093/ofid/ofy280 |
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author | Gallagher, Jason C Satlin, Michael J Elabor, Abdulrahman Saraiya, Nidhi McCreary, Erin K Molnar, Esther El-Beyrouty, Claudine Jones, Bruce M Dixit, Deepali Heil, Emily L Claeys, Kimberly C Hiles, Jon Vyas, Nikunj M Bland, Christopher M Suh, Jin Biason, Kenneth McCoy, Dorothy King, Madeline A Richards, Lynette Harrington, Nicole Guo, Yi Chaudhry, Saira Lu, Xiaoning Yu, Daohai |
author_facet | Gallagher, Jason C Satlin, Michael J Elabor, Abdulrahman Saraiya, Nidhi McCreary, Erin K Molnar, Esther El-Beyrouty, Claudine Jones, Bruce M Dixit, Deepali Heil, Emily L Claeys, Kimberly C Hiles, Jon Vyas, Nikunj M Bland, Christopher M Suh, Jin Biason, Kenneth McCoy, Dorothy King, Madeline A Richards, Lynette Harrington, Nicole Guo, Yi Chaudhry, Saira Lu, Xiaoning Yu, Daohai |
author_sort | Gallagher, Jason C |
collection | PubMed |
description | BACKGROUND: Multidrug-resistant Pseudomonas aeruginosa infections remain common in hospitals worldwide. We investigated the outcomes associated with the use of ceftolozane-tazobactam for the treatment of these infections. METHODS: Data were collected retrospectively from 20 hospitals across the United States about adults who received ceftolozane-tazobactam for the treatment of multidrug-resistant P aeruginosa infections of any source for at least 24 hours. The primary outcome was a composite of 30-day and inpatient mortality, and secondary outcomes were clinical success and microbiological cure. Multivariable regression analysis was conducted to determine factors associated with outcomes. RESULTS: Two-hundred five patients were included in the study. Severe illness and high degrees of comorbidity were common, with median Acute Physiology and Chronic Health Evaluation (APACHE) II scores of 19 (interquartile range [IQR], 11–24) and median Charlson Comorbidity Indexes of 4 (IQR, 3–6). Delayed initiation of ceftolozane-tazobactam was common with therapy started a median of 9 days after culture collection. Fifty-nine percent of patients had pneumonia. On susceptibility testing, 125 of 139 (89.9%) isolates were susceptible to ceftolozane-tazobactam. Mortality occurred in 39 patients (19%); clinical success and microbiological cure were 151 (73.7%) and 145 (70.7%), respectively. On multivariable regression analysis, starting ceftolozane-tazobactam within 4 days of culture collection was associated with survival (adjusted odds ratio [OR], 5.55; 95% confidence interval [CI], 2.14–14.40), clinical success (adjusted OR, 2.93; 95% CI, 1.40–6.10), and microbiological cure (adjusted OR, 2.59; 95% CI, 1.24–5.38). CONCLUSIONS: Ceftolozane-tazobactam appeared to be effective in the treatment of multidrug-resistant P aeruginosa infections, particularly when initiated early after the onset of infection. |
format | Online Article Text |
id | pubmed-6247659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62476592018-11-28 Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: A Multicenter Study Gallagher, Jason C Satlin, Michael J Elabor, Abdulrahman Saraiya, Nidhi McCreary, Erin K Molnar, Esther El-Beyrouty, Claudine Jones, Bruce M Dixit, Deepali Heil, Emily L Claeys, Kimberly C Hiles, Jon Vyas, Nikunj M Bland, Christopher M Suh, Jin Biason, Kenneth McCoy, Dorothy King, Madeline A Richards, Lynette Harrington, Nicole Guo, Yi Chaudhry, Saira Lu, Xiaoning Yu, Daohai Open Forum Infect Dis Major Articles BACKGROUND: Multidrug-resistant Pseudomonas aeruginosa infections remain common in hospitals worldwide. We investigated the outcomes associated with the use of ceftolozane-tazobactam for the treatment of these infections. METHODS: Data were collected retrospectively from 20 hospitals across the United States about adults who received ceftolozane-tazobactam for the treatment of multidrug-resistant P aeruginosa infections of any source for at least 24 hours. The primary outcome was a composite of 30-day and inpatient mortality, and secondary outcomes were clinical success and microbiological cure. Multivariable regression analysis was conducted to determine factors associated with outcomes. RESULTS: Two-hundred five patients were included in the study. Severe illness and high degrees of comorbidity were common, with median Acute Physiology and Chronic Health Evaluation (APACHE) II scores of 19 (interquartile range [IQR], 11–24) and median Charlson Comorbidity Indexes of 4 (IQR, 3–6). Delayed initiation of ceftolozane-tazobactam was common with therapy started a median of 9 days after culture collection. Fifty-nine percent of patients had pneumonia. On susceptibility testing, 125 of 139 (89.9%) isolates were susceptible to ceftolozane-tazobactam. Mortality occurred in 39 patients (19%); clinical success and microbiological cure were 151 (73.7%) and 145 (70.7%), respectively. On multivariable regression analysis, starting ceftolozane-tazobactam within 4 days of culture collection was associated with survival (adjusted odds ratio [OR], 5.55; 95% confidence interval [CI], 2.14–14.40), clinical success (adjusted OR, 2.93; 95% CI, 1.40–6.10), and microbiological cure (adjusted OR, 2.59; 95% CI, 1.24–5.38). CONCLUSIONS: Ceftolozane-tazobactam appeared to be effective in the treatment of multidrug-resistant P aeruginosa infections, particularly when initiated early after the onset of infection. Oxford University Press 2018-10-31 /pmc/articles/PMC6247659/ /pubmed/30488041 http://dx.doi.org/10.1093/ofid/ofy280 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Major Articles Gallagher, Jason C Satlin, Michael J Elabor, Abdulrahman Saraiya, Nidhi McCreary, Erin K Molnar, Esther El-Beyrouty, Claudine Jones, Bruce M Dixit, Deepali Heil, Emily L Claeys, Kimberly C Hiles, Jon Vyas, Nikunj M Bland, Christopher M Suh, Jin Biason, Kenneth McCoy, Dorothy King, Madeline A Richards, Lynette Harrington, Nicole Guo, Yi Chaudhry, Saira Lu, Xiaoning Yu, Daohai Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: A Multicenter Study |
title | Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: A Multicenter Study |
title_full | Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: A Multicenter Study |
title_fullStr | Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: A Multicenter Study |
title_full_unstemmed | Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: A Multicenter Study |
title_short | Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: A Multicenter Study |
title_sort | ceftolozane-tazobactam for the treatment of multidrug-resistant pseudomonas aeruginosa infections: a multicenter study |
topic | Major Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247659/ https://www.ncbi.nlm.nih.gov/pubmed/30488041 http://dx.doi.org/10.1093/ofid/ofy280 |
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