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The safety of ceftolozane-tazobactam for the treatment of acute bacterial infections: a systemic review and meta-analysis

OBJECTIVE(S): The aim of this study was to conduct a meta-analysis to assess the clinical safety of ceftolozane-tazobactam for the treatment of acute bacterial infections in adult patients. METHODS: The PubMed, Embase, and Cochrane databases were searched from their inception until May 2020 for rele...

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Autores principales: Wang, Li-Ting, Lin, Wei-Ting, Lai, Chih-Cheng, Wang, Ya-Hui, Chen, Cheng-Hsin, Chang, Yen-Teh, Chen, Chao-Hsien, Wang, Cheng-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290504/
https://www.ncbi.nlm.nih.gov/pubmed/34349976
http://dx.doi.org/10.1177/20420986211027096
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author Wang, Li-Ting
Lin, Wei-Ting
Lai, Chih-Cheng
Wang, Ya-Hui
Chen, Cheng-Hsin
Chang, Yen-Teh
Chen, Chao-Hsien
Wang, Cheng-Yi
author_facet Wang, Li-Ting
Lin, Wei-Ting
Lai, Chih-Cheng
Wang, Ya-Hui
Chen, Cheng-Hsin
Chang, Yen-Teh
Chen, Chao-Hsien
Wang, Cheng-Yi
author_sort Wang, Li-Ting
collection PubMed
description OBJECTIVE(S): The aim of this study was to conduct a meta-analysis to assess the clinical safety of ceftolozane-tazobactam for the treatment of acute bacterial infections in adult patients. METHODS: The PubMed, Embase, and Cochrane databases were searched from their inception until May 2020 for relevant randomized controlled trials (RCTs). Only RCTs evaluating the risk of adverse events (AEs) for ceftolozane-tazobactam and comparative treatments for acute bacterial infections in adult patients were included. RESULTS: Overall, four RCTs including a total of 2924 patients (1475 in the ceftolozane-tazobactam group and 1449 in the control group) were included in the meta-analysis. The rate of treatment-emergent AEs was 51.3% (748/1458) in the ceftolozane-tazobactam group, which was comparable to the control group, 49.9% [714/1430; odd’s ratio (OR), 1.06; 95% confidence interval (CI), 0.91–1.25; I(2) = 0%]. In addition, no difference was observed between the ceftolozane-tazobactam and control groups in terms of the risk of serious AEs (OR, 1.22; 95% CI, 0.93–1.61; I(2) = 15.5%) and the risk of discontinuing the study drug due to AEs (OR, 0.85; 95% CI, 0.55–1.33; I(2) = 0%). The rate of all-cause mortality did not significantly differ between the ceftolozane-tazobactam and control groups (OR, 1.11; 95% CI, 0.82–1.50; I(2) = 0%). The only exception was the risk of Clostridiodes difficile (C. difficile) colitis, where ceftolozane-tazobactam treatment was associated with a significantly higher risk compared with the control group [0.72% (10/1376) versus 0.14% (2/1391), OR, 3.84; 95% CI, 1.23–11.97; I(2) = 0%]. CONCLUSION: Ceftolozane-tazobactam treatment is as tolerable as comparative treatment options for acute bacterial infections in adult patients, however it has an increased risk of C. difficile infection. As a novel broad-spectrum antibiotic, ceftolozane-tazobactam could be a safe therapeutic option for use in common clinical practice. PLAIN LANGUAGE SUMMARY: The safety of ceftolozane-tazobactam (an antibiotics) for the treatment of acute bacterial infections Objective(s): Ceftolozane-tazobactam is an effective antibiotic for the treatment of acute bacterial infections. This study conducts a meta-analysis to assess the clinical safety (side effects) of ceftolozane-tazobactam for the treatment of acute bacterial infections in adult patients compared with other drugs. Methods: We extracted data from four randomized controlled trials, including a total of 2924 patients (1475 in the ceftolozane-tazobactam group and 1449 in the control group). Results: The rate of treatment related adverse events (AEs) was similar in the ceftolozane-tazobactam group (51.3%) and control group (49.9%). There was also no difference in risk of serious adverse events, the risk of discontinuing the study drug due to AEs, and all-cause mortality. The only exception was the risk of Clostridiodes difficile colitis (a cause of antibiotic-associated diarrhea), where ceftolozane-tazobactam treatment was associated with a significantly higher risk compared with the control group. Conclusion: In conclusion, as a novel broad-spectrum antibiotic, ceftolozane-tazobactam could be a safe therapeutic option for use in clinical practice.
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spelling pubmed-82905042021-08-03 The safety of ceftolozane-tazobactam for the treatment of acute bacterial infections: a systemic review and meta-analysis Wang, Li-Ting Lin, Wei-Ting Lai, Chih-Cheng Wang, Ya-Hui Chen, Cheng-Hsin Chang, Yen-Teh Chen, Chao-Hsien Wang, Cheng-Yi Ther Adv Drug Saf Meta-Analysis OBJECTIVE(S): The aim of this study was to conduct a meta-analysis to assess the clinical safety of ceftolozane-tazobactam for the treatment of acute bacterial infections in adult patients. METHODS: The PubMed, Embase, and Cochrane databases were searched from their inception until May 2020 for relevant randomized controlled trials (RCTs). Only RCTs evaluating the risk of adverse events (AEs) for ceftolozane-tazobactam and comparative treatments for acute bacterial infections in adult patients were included. RESULTS: Overall, four RCTs including a total of 2924 patients (1475 in the ceftolozane-tazobactam group and 1449 in the control group) were included in the meta-analysis. The rate of treatment-emergent AEs was 51.3% (748/1458) in the ceftolozane-tazobactam group, which was comparable to the control group, 49.9% [714/1430; odd’s ratio (OR), 1.06; 95% confidence interval (CI), 0.91–1.25; I(2) = 0%]. In addition, no difference was observed between the ceftolozane-tazobactam and control groups in terms of the risk of serious AEs (OR, 1.22; 95% CI, 0.93–1.61; I(2) = 15.5%) and the risk of discontinuing the study drug due to AEs (OR, 0.85; 95% CI, 0.55–1.33; I(2) = 0%). The rate of all-cause mortality did not significantly differ between the ceftolozane-tazobactam and control groups (OR, 1.11; 95% CI, 0.82–1.50; I(2) = 0%). The only exception was the risk of Clostridiodes difficile (C. difficile) colitis, where ceftolozane-tazobactam treatment was associated with a significantly higher risk compared with the control group [0.72% (10/1376) versus 0.14% (2/1391), OR, 3.84; 95% CI, 1.23–11.97; I(2) = 0%]. CONCLUSION: Ceftolozane-tazobactam treatment is as tolerable as comparative treatment options for acute bacterial infections in adult patients, however it has an increased risk of C. difficile infection. As a novel broad-spectrum antibiotic, ceftolozane-tazobactam could be a safe therapeutic option for use in common clinical practice. PLAIN LANGUAGE SUMMARY: The safety of ceftolozane-tazobactam (an antibiotics) for the treatment of acute bacterial infections Objective(s): Ceftolozane-tazobactam is an effective antibiotic for the treatment of acute bacterial infections. This study conducts a meta-analysis to assess the clinical safety (side effects) of ceftolozane-tazobactam for the treatment of acute bacterial infections in adult patients compared with other drugs. Methods: We extracted data from four randomized controlled trials, including a total of 2924 patients (1475 in the ceftolozane-tazobactam group and 1449 in the control group). Results: The rate of treatment related adverse events (AEs) was similar in the ceftolozane-tazobactam group (51.3%) and control group (49.9%). There was also no difference in risk of serious adverse events, the risk of discontinuing the study drug due to AEs, and all-cause mortality. The only exception was the risk of Clostridiodes difficile colitis (a cause of antibiotic-associated diarrhea), where ceftolozane-tazobactam treatment was associated with a significantly higher risk compared with the control group. Conclusion: In conclusion, as a novel broad-spectrum antibiotic, ceftolozane-tazobactam could be a safe therapeutic option for use in clinical practice. SAGE Publications 2021-07-15 /pmc/articles/PMC8290504/ /pubmed/34349976 http://dx.doi.org/10.1177/20420986211027096 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Meta-Analysis
Wang, Li-Ting
Lin, Wei-Ting
Lai, Chih-Cheng
Wang, Ya-Hui
Chen, Cheng-Hsin
Chang, Yen-Teh
Chen, Chao-Hsien
Wang, Cheng-Yi
The safety of ceftolozane-tazobactam for the treatment of acute bacterial infections: a systemic review and meta-analysis
title The safety of ceftolozane-tazobactam for the treatment of acute bacterial infections: a systemic review and meta-analysis
title_full The safety of ceftolozane-tazobactam for the treatment of acute bacterial infections: a systemic review and meta-analysis
title_fullStr The safety of ceftolozane-tazobactam for the treatment of acute bacterial infections: a systemic review and meta-analysis
title_full_unstemmed The safety of ceftolozane-tazobactam for the treatment of acute bacterial infections: a systemic review and meta-analysis
title_short The safety of ceftolozane-tazobactam for the treatment of acute bacterial infections: a systemic review and meta-analysis
title_sort safety of ceftolozane-tazobactam for the treatment of acute bacterial infections: a systemic review and meta-analysis
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290504/
https://www.ncbi.nlm.nih.gov/pubmed/34349976
http://dx.doi.org/10.1177/20420986211027096
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