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Fluoroquinolones in the treatment of cystic fibrosis

N Høiby1, S S Pedersen, T Jensen

  • 1Department of Clinical Microbiology, Rigshospitalet, Copenhagen, Denmark.

Drugs
|January 1, 1993
PubMed

Insights

Fluoroquinolones like ciprofloxacin are effective oral treatments for Pseudomonas aeruginosa lung infections in cystic fibrosis patients. However, the increasing development of bacterial resistance is a growing concern for this important therapy.

Area of Science:

  • Medical Microbiology
  • Pulmonology
  • Infectious Diseases

Background:

  • Cystic fibrosis (CF) patients experience frequent lung infections.
  • Key pathogens include Staphylococcus aureus, Haemophilus influenzae, and Pseudomonas aeruginosa.
  • Pseudomonas aeruginosa is a major cause of morbidity and mortality in CF.

Purpose of the Study:

  • To evaluate the role of fluoroquinolones in treating P. aeruginosa infections in CF.
  • To assess the efficacy and safety of oral fluoroquinolones for CF lung infections.
  • To highlight the challenge of antimicrobial resistance.

Main Methods:

  • Review of existing literature on fluoroquinolone use in CF.
  • Analysis of treatment outcomes for P. aeruginosa infections.
  • Assessment of adverse effects and resistance patterns.

Main Results:

  • Fluoroquinolones (ciprofloxacin, ofloxacin) provide effective oral therapy for P. aeruginosa.
  • Treatment is suitable for early colonization and chronic infections, including in children.
  • Adverse effects are generally mild.
  • Increasing bacterial resistance to fluoroquinolones is a significant issue.

Conclusions:

  • Fluoroquinolones are valuable for managing P. aeruginosa in CF.
  • Oral administration offers treatment convenience.
  • Antimicrobial stewardship is crucial due to rising resistance.

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