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Revisiting cefditoren for the treatment of community-acquired infections caused by human-adapted respiratory pathogens in adults

Fifteen years after its licensure, this revision assesses the role of cefditoren facing the current pharmacoepidemiology of resistances in respiratory human-adapted pathogens (Streptococcus pneumoniae, Streptococcus pyogenes, Haemophilus influenzae and Moraxella catarrhalis). In the era of post- pne...

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Autores principales: Giménez, María-José, Aguilar, Lorenzo, Granizo, Juan José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214181/
https://www.ncbi.nlm.nih.gov/pubmed/30410757
http://dx.doi.org/10.1186/s40248-018-0152-5
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author Giménez, María-José
Aguilar, Lorenzo
Granizo, Juan José
author_facet Giménez, María-José
Aguilar, Lorenzo
Granizo, Juan José
author_sort Giménez, María-José
collection PubMed
description Fifteen years after its licensure, this revision assesses the role of cefditoren facing the current pharmacoepidemiology of resistances in respiratory human-adapted pathogens (Streptococcus pneumoniae, Streptococcus pyogenes, Haemophilus influenzae and Moraxella catarrhalis). In the era of post- pneumococcal conjugate vaccines and in an environment of increasing diffusion of the ftsI gene among H. influenzae isolates, published studies on the cefditoren in vitro microbiological activity, pharmacokinetic/pharmcodynamic (PK/PD) activity and clinical efficacy are reviewed. Based on published data, an overall analysis is performed for PK/PD susceptibility interpretation. Further translation of PK/PD data into clinical/microbiological outcomes obtained in clinical trials carried out in the respiratory indications approved for cefditoren in adults (tonsillitis, sinusitis, acute exacerbation of chronic bronchitis and community-acquired pneumonia) is commented. Finally, the role of cefditoren within the current antibiotic armamentarium for the treatment of community respiratory tract infections in adults is discussed based on the revised information on its intrinsic activity, pharmacodynamic adequacy and clinical/bacteriological efficacy. Cefditoren remains an option to be taken into account when selecting an oral antibiotic for the empirical treatment of respiratory infections in the community caused by human-adapted pathogens, even when considering changes in the pharmacoepidemiology of resistances over the last two decades.
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spelling pubmed-62141812018-11-08 Revisiting cefditoren for the treatment of community-acquired infections caused by human-adapted respiratory pathogens in adults Giménez, María-José Aguilar, Lorenzo Granizo, Juan José Multidiscip Respir Med Review Fifteen years after its licensure, this revision assesses the role of cefditoren facing the current pharmacoepidemiology of resistances in respiratory human-adapted pathogens (Streptococcus pneumoniae, Streptococcus pyogenes, Haemophilus influenzae and Moraxella catarrhalis). In the era of post- pneumococcal conjugate vaccines and in an environment of increasing diffusion of the ftsI gene among H. influenzae isolates, published studies on the cefditoren in vitro microbiological activity, pharmacokinetic/pharmcodynamic (PK/PD) activity and clinical efficacy are reviewed. Based on published data, an overall analysis is performed for PK/PD susceptibility interpretation. Further translation of PK/PD data into clinical/microbiological outcomes obtained in clinical trials carried out in the respiratory indications approved for cefditoren in adults (tonsillitis, sinusitis, acute exacerbation of chronic bronchitis and community-acquired pneumonia) is commented. Finally, the role of cefditoren within the current antibiotic armamentarium for the treatment of community respiratory tract infections in adults is discussed based on the revised information on its intrinsic activity, pharmacodynamic adequacy and clinical/bacteriological efficacy. Cefditoren remains an option to be taken into account when selecting an oral antibiotic for the empirical treatment of respiratory infections in the community caused by human-adapted pathogens, even when considering changes in the pharmacoepidemiology of resistances over the last two decades. BioMed Central 2018-11-02 /pmc/articles/PMC6214181/ /pubmed/30410757 http://dx.doi.org/10.1186/s40248-018-0152-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Giménez, María-José
Aguilar, Lorenzo
Granizo, Juan José
Revisiting cefditoren for the treatment of community-acquired infections caused by human-adapted respiratory pathogens in adults
title Revisiting cefditoren for the treatment of community-acquired infections caused by human-adapted respiratory pathogens in adults
title_full Revisiting cefditoren for the treatment of community-acquired infections caused by human-adapted respiratory pathogens in adults
title_fullStr Revisiting cefditoren for the treatment of community-acquired infections caused by human-adapted respiratory pathogens in adults
title_full_unstemmed Revisiting cefditoren for the treatment of community-acquired infections caused by human-adapted respiratory pathogens in adults
title_short Revisiting cefditoren for the treatment of community-acquired infections caused by human-adapted respiratory pathogens in adults
title_sort revisiting cefditoren for the treatment of community-acquired infections caused by human-adapted respiratory pathogens in adults
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214181/
https://www.ncbi.nlm.nih.gov/pubmed/30410757
http://dx.doi.org/10.1186/s40248-018-0152-5
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