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

María-José Giménez, Lorenzo Aguilar, Juan José Granizo
Author Information
  1. María-José Giménez: Research Department, PRISM-AG, Don Ramón de la Cruz 72, 28006 Madrid, Spain.
  2. Lorenzo Aguilar: Research Department, PRISM-AG, Don Ramón de la Cruz 72, 28006 Madrid, Spain.
  3. Juan José Granizo: 2Preventive Medicine Department, Hospital Universitario Infanta Cristina, Parla, Madrid, Spain.

Abstract

Fifteen years after its licensure, this revision assesses the role of cefditoren facing the current pharmacoepidemiology of resistances in respiratory human-adapted pathogens (, , and ). In the era of post- pneumococcal conjugate vaccines and in an environment of increasing diffusion of the I gene among 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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