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Real-world use of ceftolozane/tazobactam: a systematic literature review

BACKGROUND: Antibacterial-resistant gram-negative infections are a serious risk to global public health. Resistant Enterobacterales and Pseudomonas aeruginosa are highly prevalent, particularly in healthcare settings, and there are limited effective treatment options. Patients with infections caused...

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Autores principales: Puzniak, Laura, Dillon, Ryan, Palmer, Thomas, Collings, Hannah, Enstone, Ashley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027296/
https://www.ncbi.nlm.nih.gov/pubmed/33832545
http://dx.doi.org/10.1186/s13756-021-00933-8
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author Puzniak, Laura
Dillon, Ryan
Palmer, Thomas
Collings, Hannah
Enstone, Ashley
author_facet Puzniak, Laura
Dillon, Ryan
Palmer, Thomas
Collings, Hannah
Enstone, Ashley
author_sort Puzniak, Laura
collection PubMed
description BACKGROUND: Antibacterial-resistant gram-negative infections are a serious risk to global public health. Resistant Enterobacterales and Pseudomonas aeruginosa are highly prevalent, particularly in healthcare settings, and there are limited effective treatment options. Patients with infections caused by resistant pathogens have considerably worse outcomes, and incur significantly higher costs, relative to patients with susceptible infections. Ceftolozane/tazobactam (C/T) has established efficacy in clinical trials. This review aimed to collate data on C/T use in clinical practice. METHODS: This systematic literature review searched online biomedical databases for real-world studies of C/T for gram-negative infections up to June 2020. Relevant study, patient, and treatment characteristics, microbiology, and efficacy outcomes were captured. RESULTS: There were 83 studies comprising 3,701 patients were identified. The most common infections were respiratory infections (52.9% of reported infections), urinary tract infections (UTIs; 14.9%), and intra-abdominal infections (IAIs; 10.1%). Most patients included were seriously ill and had multiple comorbidities. The majority of patients had infections caused by P. aeruginosa (90.7%), of which 86.0% were antimicrobial-resistant. C/T was used as both a 1.5 g q8h and 3 g q8h dose, for a median duration of 7–56 days (varying between studies). Outcome rates were comparable between studies: clinical success rates ranged from 45.7 to 100.0%, with 27 studies (69%) reporting clinical success rates of > 70%; microbiological success rates ranged from 31 to 100%, with 14 studies (74%) reporting microbiological success rates of > 70%. Mortality rates ranged from 0 to 50%, with 31 studies (69%) reporting mortality rates of ≤ 20%. In comparative studies, C/T was as effective as aminoglycoside- or polymyxin-based regimens, and in some instances, significantly more effective. CONCLUSIONS: The studies identified in this review demonstrate that C/T is effective in clinical practice, despite the diverse group of seriously ill patients, different levels of resistance of the pathogens treated, and varying dosing regimens used. Furthermore, comparative studies suggest that C/T offers a successful alternative to standard of care (SoC). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13756-021-00933-8.
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spelling pubmed-80272962021-04-08 Real-world use of ceftolozane/tazobactam: a systematic literature review Puzniak, Laura Dillon, Ryan Palmer, Thomas Collings, Hannah Enstone, Ashley Antimicrob Resist Infect Control Research BACKGROUND: Antibacterial-resistant gram-negative infections are a serious risk to global public health. Resistant Enterobacterales and Pseudomonas aeruginosa are highly prevalent, particularly in healthcare settings, and there are limited effective treatment options. Patients with infections caused by resistant pathogens have considerably worse outcomes, and incur significantly higher costs, relative to patients with susceptible infections. Ceftolozane/tazobactam (C/T) has established efficacy in clinical trials. This review aimed to collate data on C/T use in clinical practice. METHODS: This systematic literature review searched online biomedical databases for real-world studies of C/T for gram-negative infections up to June 2020. Relevant study, patient, and treatment characteristics, microbiology, and efficacy outcomes were captured. RESULTS: There were 83 studies comprising 3,701 patients were identified. The most common infections were respiratory infections (52.9% of reported infections), urinary tract infections (UTIs; 14.9%), and intra-abdominal infections (IAIs; 10.1%). Most patients included were seriously ill and had multiple comorbidities. The majority of patients had infections caused by P. aeruginosa (90.7%), of which 86.0% were antimicrobial-resistant. C/T was used as both a 1.5 g q8h and 3 g q8h dose, for a median duration of 7–56 days (varying between studies). Outcome rates were comparable between studies: clinical success rates ranged from 45.7 to 100.0%, with 27 studies (69%) reporting clinical success rates of > 70%; microbiological success rates ranged from 31 to 100%, with 14 studies (74%) reporting microbiological success rates of > 70%. Mortality rates ranged from 0 to 50%, with 31 studies (69%) reporting mortality rates of ≤ 20%. In comparative studies, C/T was as effective as aminoglycoside- or polymyxin-based regimens, and in some instances, significantly more effective. CONCLUSIONS: The studies identified in this review demonstrate that C/T is effective in clinical practice, despite the diverse group of seriously ill patients, different levels of resistance of the pathogens treated, and varying dosing regimens used. Furthermore, comparative studies suggest that C/T offers a successful alternative to standard of care (SoC). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13756-021-00933-8. BioMed Central 2021-04-08 /pmc/articles/PMC8027296/ /pubmed/33832545 http://dx.doi.org/10.1186/s13756-021-00933-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Puzniak, Laura
Dillon, Ryan
Palmer, Thomas
Collings, Hannah
Enstone, Ashley
Real-world use of ceftolozane/tazobactam: a systematic literature review
title Real-world use of ceftolozane/tazobactam: a systematic literature review
title_full Real-world use of ceftolozane/tazobactam: a systematic literature review
title_fullStr Real-world use of ceftolozane/tazobactam: a systematic literature review
title_full_unstemmed Real-world use of ceftolozane/tazobactam: a systematic literature review
title_short Real-world use of ceftolozane/tazobactam: a systematic literature review
title_sort real-world use of ceftolozane/tazobactam: a systematic literature review
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027296/
https://www.ncbi.nlm.nih.gov/pubmed/33832545
http://dx.doi.org/10.1186/s13756-021-00933-8
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