Indications and Usage Guidelines for Fluoroquinolones
Fluoroquinolones should be restricted to situations where there is no safe and effective alternative to treat an infection caused by multidrug-resistant bacteria or when parenteral therapy is not feasible and no other effective oral agent is available. 1
Primary Indications
- Urinary Tract Infections: Fluoroquinolones remain a potential first-line agent only for complicated UTIs or pyelonephritis when typically recommended agents are not appropriate based on susceptibility data, allergy, or adverse-event history 1
- Respiratory Infections:
- Intra-abdominal Infections: Moxifloxacin is recommended by IDSA for mild-to-moderate complicated intra-abdominal infections, though not recommended in areas with high fluoroquinolone resistance rates (>20%) 1
- Neutropenic Patients: Fluoroquinolone prophylaxis should be considered for high-risk patients with expected durations of prolonged and profound neutropenia (ANC <100 cells/mm³ for >7 days) 1
Special Indications
- Multidrug-resistant tuberculosis: Fluoroquinolones (particularly levofloxacin and moxifloxacin) have demonstrated bactericidal activity against M. tuberculosis and are used in multidrug-resistant TB regimens 1
- Pseudomonas infections: Ciprofloxacin has particular utility for Pseudomonas aeruginosa infections, including skin infections following exposure to inadequately chlorinated swimming pools or hot tubs 1
- Traveler's diarrhea: Though historically effective, increasing resistance rates limit current utility, particularly in countries like Taiwan, Thailand, and Sweden 1
- Meningococcal carriage eradication: Ciprofloxacin is effective in eradicating nasal carriage of Neisseria meningitidis 1
Selection Guidelines
- Ciprofloxacin: Preferred for Gram-negative infections, particularly those involving Pseudomonas aeruginosa 6
- Levofloxacin: Balanced activity against both Gram-positive and Gram-negative pathogens 4, 5
- Moxifloxacin: Enhanced activity against respiratory pathogens, particularly S. pneumoniae 6
Resistance Considerations
- Local resistance patterns should guide empiric use - fluoroquinolones should only be used empirically when local resistance rates are below 10% 7
- Fluoroquinolone resistance in Campylobacter species is particularly problematic in countries such as Taiwan (57%), Thailand (84%), and Sweden (up to 88%) 1
- A systematic strategy for monitoring the development of fluoroquinolone resistance among gram-negative bacilli is recommended 1
Pediatric Considerations
- FDA-approved pediatric indications are limited to:
- Complicated urinary tract infections
- Pyelonephritis
- Post-exposure treatment for inhalation anthrax 1
- Despite limited approval, approximately 520,000 prescriptions for fluoroquinolones were written for children and adolescents in the United States in 2002 1
- Fluoroquinolones should be restricted in children to situations where no safe and effective alternative exists 1
Safety Concerns
- Arthropathy in juvenile animals has been a consistent finding with most fluoroquinolones 1
- Other adverse events include:
- Central nervous system disorders (nervousness, agitation, insomnia) 3
- Photosensitivity/phototoxicity reactions 3
- Disorders of glucose homeostasis 3
- QT interval prolongation 1
- Hepatic dysfunction 3
- Tendinopathy, particularly in older patients, those taking corticosteroids, and patients with kidney, heart or lung transplants 3
Treatment Duration Guidelines
- For documented infections, therapy should continue for at least the duration of neutropenia (until ANC >500 cells/mm³) or longer if clinically necessary 1
- For community-acquired pneumonia: 7-14 days for standard regimens, 5 days for specific pathogens 2
- For complicated UTIs: 7-10 days 7
Common Pitfalls to Avoid
- Using fluoroquinolones as first-line therapy when other effective and safer alternatives are available 1
- Ignoring local resistance patterns when selecting empiric therapy 7
- Not obtaining cultures before initiating therapy for suspected complicated infections 7
- Inadequate duration of therapy for complicated infections 7
- Failing to monitor for adverse effects, particularly in high-risk populations 3
By following these guidelines, clinicians can optimize the use of fluoroquinolones while helping to preserve their efficacy and minimize the development of resistance.